• Human bipedalism

    From jillery@21:1/5 to All on Mon Oct 24 02:50:19 2022
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Mon Oct 24 08:50:51 2022
    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    Thanks I added a couple comments.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Trolidan7@21:1/5 to jillery on Tue Oct 25 01:18:27 2022
    On 10/23/22 11:50 PM, jillery wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    I tend to think of it as none of the above.

    Simply because it is not that easy to stand upright.

    When an animal stands upright you need to solve a problem -
    how do you keep from falling over forward and backward.

    This might seem simple but it is not because with a four
    footed animal the center of gravity forward and backward
    is between the front legs and the back legs, and often
    that is a greater distance than between the left legs and
    the right legs.

    Some animals that sort of walk on twos have not solved the
    problem - a kangaroo can hop but in general it can not
    stably stand. Either way, in essence, the long hand enables
    force to be supplied to the far front and far back to counter
    falling forward or backward - the forefoot and big toe are
    the front force appliers and the heel is the back force
    applier. Then of course there are some animals that might
    sort of walk on threes (I am thinking of the Jerboa) - but
    humans have an extra problem because they have no tail to
    possibly act as an extra walking limb, or at least a balance.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to Trolidan7@eternal-september.org on Tue Oct 25 18:59:02 2022
    On Tue, 25 Oct 2022 01:18:27 -0700, Trolidan7
    <Trolidan7@eternal-september.org> wrote:

    On 10/23/22 11:50 PM, jillery wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    I tend to think of it as none of the above.

    Simply because it is not that easy to stand upright.

    When an animal stands upright you need to solve a problem -
    how do you keep from falling over forward and backward.

    This might seem simple but it is not because with a four
    footed animal the center of gravity forward and backward
    is between the front legs and the back legs, and often
    that is a greater distance than between the left legs and
    the right legs.


    Watch the cited videos. Erika points out the challenges of going from quadruped to biped, the differences between upright posture and
    bipedalism, and the plausibility of suspensory orthograde posture in
    trees as a precursor to bipedalism on the ground.


    Some animals that sort of walk on twos have not solved the
    problem - a kangaroo can hop but in general it can not
    stably stand. Either way, in essence, the long hand enables
    force to be supplied to the far front and far back to counter
    falling forward or backward - the forefoot and big toe are
    the front force appliers and the heel is the back force
    applier. Then of course there are some animals that might
    sort of walk on threes (I am thinking of the Jerboa) - but
    humans have an extra problem because they have no tail to
    possibly act as an extra walking limb, or at least a balance.


    That's why humans like big butts, I can not lie.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Tue Oct 25 16:32:06 2022
    On Tuesday, October 25, 2022 at 6:59:05 PM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 01:18:27 -0700, Trolidan7 <Trol...@eternal-september.org> wrote:

    On 10/23/22 11:50 PM, jillery wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    I tend to think of it as none of the above.

    Simply because it is not that easy to stand upright.

    When an animal stands upright you need to solve a problem -
    how do you keep from falling over forward and backward.

    This might seem simple but it is not because with a four
    footed animal the center of gravity forward and backward
    is between the front legs and the back legs, and often
    that is a greater distance than between the left legs and
    the right legs.
    Watch the cited videos. Erika points out the challenges of going from quadruped to biped, the differences between upright posture and
    bipedalism, and the plausibility of suspensory orthograde posture in
    trees as a precursor to bipedalism on the ground.
    Some animals that sort of walk on twos have not solved the
    problem - a kangaroo can hop but in general it can not
    stably stand. Either way, in essence, the long hand enables
    force to be supplied to the far front and far back to counter
    falling forward or backward - the forefoot and big toe are
    the front force appliers and the heel is the back force
    applier. Then of course there are some animals that might
    sort of walk on threes (I am thinking of the Jerboa) - but
    humans have an extra problem because they have no tail to
    possibly act as an extra walking limb, or at least a balance.
    That's why humans like big butts, I can not lie.

    Bigger butt bones, bigger brain bones, initially.
    Homo erectus had unusually thick dense femurs and unusually thick dense occiputs (rear skull bone), which counterbalanced the pace over orthogonal bipedal treks on the ground, substituting for the more typical long dense tail of other bipeds (T rex,
    giant short faced kangaroo, giant ground sloth, running jesus lizard). This primitive mechanical gyroscope was replaced by genetic software improvements enabling reduced body bone weight (esp. femur & occiput), faster & longer bipedal locomotion,
    drastically reduced climbing/brachiating abilities.

    Casually walking while chewing gum, chatting and carrying a squirming child is something only humans could ever do.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to daud.deden@gmail.com on Wed Oct 26 04:10:45 2022
    On Tue, 25 Oct 2022 16:32:06 -0700 (PDT), Daud Deden
    <daud.deden@gmail.com> wrote:

    On Tuesday, October 25, 2022 at 6:59:05 PM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 01:18:27 -0700, Trolidan7
    <Trol...@eternal-september.org> wrote:

    On 10/23/22 11:50 PM, jillery wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several >> >> papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several >> >> hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    I tend to think of it as none of the above.

    Simply because it is not that easy to stand upright.

    When an animal stands upright you need to solve a problem -
    how do you keep from falling over forward and backward.

    This might seem simple but it is not because with a four
    footed animal the center of gravity forward and backward
    is between the front legs and the back legs, and often
    that is a greater distance than between the left legs and
    the right legs.
    Watch the cited videos. Erika points out the challenges of going from
    quadruped to biped, the differences between upright posture and
    bipedalism, and the plausibility of suspensory orthograde posture in
    trees as a precursor to bipedalism on the ground.
    Some animals that sort of walk on twos have not solved the
    problem - a kangaroo can hop but in general it can not
    stably stand. Either way, in essence, the long hand enables
    force to be supplied to the far front and far back to counter
    falling forward or backward - the forefoot and big toe are
    the front force appliers and the heel is the back force
    applier. Then of course there are some animals that might
    sort of walk on threes (I am thinking of the Jerboa) - but
    humans have an extra problem because they have no tail to
    possibly act as an extra walking limb, or at least a balance.
    That's why humans like big butts, I can not lie.

    Bigger butt bones, bigger brain bones, initially.
    Homo erectus had unusually thick dense femurs and unusually thick dense occiputs (rear skull bone), which counterbalanced the pace over orthogonal bipedal treks on the ground, substituting for the more typical long dense tail of other bipeds (T rex,
    giant short faced kangaroo, giant ground sloth, running jesus lizard). This primitive mechanical gyroscope was replaced by genetic software improvements enabling reduced body bone weight (esp. femur & occiput), faster & longer bipedal locomotion,
    drastically reduced climbing/brachiating abilities.

    Casually walking while chewing gum, chatting and carrying a squirming child is something only humans could ever do.


    @378 cm^3, S. tchadensis' braincase is similar to that of extant
    chimpanzees and approximately a third the size of modern human brains.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Wed Oct 26 03:17:08 2022
    On Wednesday, October 26, 2022 at 4:10:49 AM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 16:32:06 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, October 25, 2022 at 6:59:05 PM UTC-4, 69jp...@gmail.com wrote: >> On Tue, 25 Oct 2022 01:18:27 -0700, Trolidan7
    <Trol...@eternal-september.org> wrote:

    On 10/23/22 11:50 PM, jillery wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD >> >> student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several >> >> papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in >> >> central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several >> >> hypotheses about *why* our ancestors shifted to obligate bipedalism. >> >> She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    I tend to think of it as none of the above.

    Simply because it is not that easy to stand upright.

    When an animal stands upright you need to solve a problem -
    how do you keep from falling over forward and backward.

    This might seem simple but it is not because with a four
    footed animal the center of gravity forward and backward
    is between the front legs and the back legs, and often
    that is a greater distance than between the left legs and
    the right legs.
    Watch the cited videos. Erika points out the challenges of going from
    quadruped to biped, the differences between upright posture and
    bipedalism, and the plausibility of suspensory orthograde posture in
    trees as a precursor to bipedalism on the ground.
    Some animals that sort of walk on twos have not solved the
    problem - a kangaroo can hop but in general it can not
    stably stand. Either way, in essence, the long hand enables
    force to be supplied to the far front and far back to counter
    falling forward or backward - the forefoot and big toe are
    the front force appliers and the heel is the back force
    applier. Then of course there are some animals that might
    sort of walk on threes (I am thinking of the Jerboa) - but
    humans have an extra problem because they have no tail to
    possibly act as an extra walking limb, or at least a balance.
    That's why humans like big butts, I can not lie.

    Bigger butt bones, bigger brain bones, initially.
    Homo erectus had unusually thick dense femurs and unusually thick dense occiputs (rear skull bone), which counterbalanced the pace over orthogonal bipedal treks on the ground, substituting for the more typical long dense tail of other bipeds (T rex,
    giant short faced kangaroo, giant ground sloth, running jesus lizard). This primitive mechanical gyroscope was replaced by genetic software improvements enabling reduced body bone weight (esp. femur & occiput), faster & longer bipedal locomotion,
    drastically reduced climbing/brachiating abilities.

    Casually walking while chewing gum, chatting and carrying a squirming child is something only humans could ever do.
    @378 cm^3, S. tchadensis' braincase is similar to that of extant
    chimpanzees and approximately a third the size of modern human brains.
    S chadensis was imo not a habitual nor obligate terrestrial orthograde biped, nor a part-time knucklewalking terrestrial quadruped, its foramen magnum reflected a more primitive arboreal orthograde bipedalism associated with suspensory slow brachiation x
    arboreal bipedalism, as in European miocene - pliocene apes and similar to but distinct from faster extant gibbons.

    Chimps & gorillas became more quadrupedal (partly pronograde terrestrial knucklewalking) while Homo became more bipedal (fully orthograde habitual obligate terrestrial striding), these produced changes of position and orientation of the foramen magnum.

    https://carta.anthropogeny.org/moca/topics/foramen-magnum-placement#:~:text=The%20foramen%20magnum%20position%20has,case%20for%20Ardipithecus%20and%20Sahelanthropus.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to daud.deden@gmail.com on Wed Oct 26 19:56:40 2022
    On Wed, 26 Oct 2022 03:17:08 -0700 (PDT), Daud Deden
    <daud.deden@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 4:10:49 AM UTC-4, 69jp...@gmail.com wrote: >> On Tue, 25 Oct 2022 16:32:06 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, October 25, 2022 at 6:59:05 PM UTC-4, 69jp...@gmail.com wrote: >> >> On Tue, 25 Oct 2022 01:18:27 -0700, Trolidan7
    <Trol...@eternal-september.org> wrote:

    On 10/23/22 11:50 PM, jillery wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD >> >> >> student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in >> >> >> central-african Chad, and also because it may be the oldest bipedal >> >> >> hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism. >> >> >> She discusses several hypotheses, and presents compelling arguments >> >> >> for her preferred one.

    I tend to think of it as none of the above.

    Simply because it is not that easy to stand upright.

    When an animal stands upright you need to solve a problem -
    how do you keep from falling over forward and backward.

    This might seem simple but it is not because with a four
    footed animal the center of gravity forward and backward
    is between the front legs and the back legs, and often
    that is a greater distance than between the left legs and
    the right legs.
    Watch the cited videos. Erika points out the challenges of going from
    quadruped to biped, the differences between upright posture and
    bipedalism, and the plausibility of suspensory orthograde posture in
    trees as a precursor to bipedalism on the ground.
    Some animals that sort of walk on twos have not solved the
    problem - a kangaroo can hop but in general it can not
    stably stand. Either way, in essence, the long hand enables
    force to be supplied to the far front and far back to counter
    falling forward or backward - the forefoot and big toe are
    the front force appliers and the heel is the back force
    applier. Then of course there are some animals that might
    sort of walk on threes (I am thinking of the Jerboa) - but
    humans have an extra problem because they have no tail to
    possibly act as an extra walking limb, or at least a balance.
    That's why humans like big butts, I can not lie.

    Bigger butt bones, bigger brain bones, initially.
    Homo erectus had unusually thick dense femurs and unusually thick dense occiputs (rear skull bone), which counterbalanced the pace over orthogonal bipedal treks on the ground, substituting for the more typical long dense tail of other bipeds (T rex,
    giant short faced kangaroo, giant ground sloth, running jesus lizard). This primitive mechanical gyroscope was replaced by genetic software improvements enabling reduced body bone weight (esp. femur & occiput), faster & longer bipedal locomotion,
    drastically reduced climbing/brachiating abilities.

    Casually walking while chewing gum, chatting and carrying a squirming child is something only humans could ever do.
    @378 cm^3, S. tchadensis' braincase is similar to that of extant
    chimpanzees and approximately a third the size of modern human brains.
    S chadensis was imo not a habitual nor obligate terrestrial orthograde biped, nor a part-time knucklewalking terrestrial quadruped, its foramen magnum reflected a more primitive arboreal orthograde bipedalism associated with suspensory slow brachiation
    x arboreal bipedalism, as in European miocene - pliocene apes and similar to but distinct from faster extant gibbons.

    Chimps & gorillas became more quadrupedal (partly pronograde terrestrial knucklewalking) while Homo became more bipedal (fully orthograde habitual obligate terrestrial striding), these produced changes of position and orientation of the foramen magnum.

    https://carta.anthropogeny.org/moca/topics/foramen-magnum-placement#:~:text=The%20foramen%20magnum%20position%20has,case%20for%20Ardipithecus%20and%20Sahelanthropus.


    The authors of the paper Erika cited disagree with your opinion.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Thu Oct 27 02:17:42 2022
    On Wednesday, October 26, 2022 at 7:56:43 PM UTC-4, 69jp...@gmail.com wrote:
    On Wed, 26 Oct 2022 03:17:08 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 4:10:49 AM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 16:32:06 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, October 25, 2022 at 6:59:05 PM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 01:18:27 -0700, Trolidan7
    <Trol...@eternal-september.org> wrote:

    On 10/23/22 11:50 PM, jillery wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the >> >> >> latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal >> >> >> hominin fossil found to date. However, there appears to be strong >> >> >> disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments >> >> >> for her preferred one.

    I tend to think of it as none of the above.

    Simply because it is not that easy to stand upright.

    When an animal stands upright you need to solve a problem -
    how do you keep from falling over forward and backward.

    This might seem simple but it is not because with a four
    footed animal the center of gravity forward and backward
    is between the front legs and the back legs, and often
    that is a greater distance than between the left legs and
    the right legs.
    Watch the cited videos. Erika points out the challenges of going from >> >> quadruped to biped, the differences between upright posture and
    bipedalism, and the plausibility of suspensory orthograde posture in >> >> trees as a precursor to bipedalism on the ground.
    Some animals that sort of walk on twos have not solved the
    problem - a kangaroo can hop but in general it can not
    stably stand. Either way, in essence, the long hand enables
    force to be supplied to the far front and far back to counter
    falling forward or backward - the forefoot and big toe are
    the front force appliers and the heel is the back force
    applier. Then of course there are some animals that might
    sort of walk on threes (I am thinking of the Jerboa) - but
    humans have an extra problem because they have no tail to
    possibly act as an extra walking limb, or at least a balance.
    That's why humans like big butts, I can not lie.

    Bigger butt bones, bigger brain bones, initially.
    Homo erectus had unusually thick dense femurs and unusually thick dense occiputs (rear skull bone), which counterbalanced the pace over orthogonal bipedal treks on the ground, substituting for the more typical long dense tail of other bipeds (T rex,
    giant short faced kangaroo, giant ground sloth, running jesus lizard). This primitive mechanical gyroscope was replaced by genetic software improvements enabling reduced body bone weight (esp. femur & occiput), faster & longer bipedal locomotion,
    drastically reduced climbing/brachiating abilities.

    Casually walking while chewing gum, chatting and carrying a squirming child is something only humans could ever do.
    @378 cm^3, S. tchadensis' braincase is similar to that of extant
    chimpanzees and approximately a third the size of modern human brains.
    S chadensis was imo not a habitual nor obligate terrestrial orthograde biped, nor a part-time knucklewalking terrestrial quadruped, its foramen magnum reflected a more primitive arboreal orthograde bipedalism associated with suspensory slow
    brachiation x arboreal bipedalism, as in European miocene - pliocene apes and similar to but distinct from faster extant gibbons.

    Chimps & gorillas became more quadrupedal (partly pronograde terrestrial knucklewalking) while Homo became more bipedal (fully orthograde habitual obligate terrestrial striding), these produced changes of position and orientation of the foramen magnum.


    https://carta.anthropogeny.org/moca/topics/foramen-magnum-placement#:~:text=The%20foramen%20magnum%20position%20has,case%20for%20Ardipithecus%20and%20Sahelanthropus.
    The authors of the paper Erika cited disagree with your opinion.
    They might
    be right.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to daud.deden@gmail.com on Thu Oct 27 05:53:01 2022
    On Thu, 27 Oct 2022 02:17:42 -0700 (PDT), Daud Deden
    <daud.deden@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 7:56:43 PM UTC-4, 69jp...@gmail.com wrote: >> On Wed, 26 Oct 2022 03:17:08 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 4:10:49 AM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 16:32:06 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, October 25, 2022 at 6:59:05 PM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 01:18:27 -0700, Trolidan7
    <Trol...@eternal-september.org> wrote:

    On 10/23/22 11:50 PM, jillery wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the >> >> >> >> latest developments relating to the origins of human bipedalism: >> >> >> >>
    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong >> >> >> >> disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    I tend to think of it as none of the above.

    Simply because it is not that easy to stand upright.

    When an animal stands upright you need to solve a problem -
    how do you keep from falling over forward and backward.

    This might seem simple but it is not because with a four
    footed animal the center of gravity forward and backward
    is between the front legs and the back legs, and often
    that is a greater distance than between the left legs and
    the right legs.
    Watch the cited videos. Erika points out the challenges of going from >> >> >> quadruped to biped, the differences between upright posture and
    bipedalism, and the plausibility of suspensory orthograde posture in >> >> >> trees as a precursor to bipedalism on the ground.
    Some animals that sort of walk on twos have not solved the
    problem - a kangaroo can hop but in general it can not
    stably stand. Either way, in essence, the long hand enables
    force to be supplied to the far front and far back to counter
    falling forward or backward - the forefoot and big toe are
    the front force appliers and the heel is the back force
    applier. Then of course there are some animals that might
    sort of walk on threes (I am thinking of the Jerboa) - but
    humans have an extra problem because they have no tail to
    possibly act as an extra walking limb, or at least a balance.
    That's why humans like big butts, I can not lie.

    Bigger butt bones, bigger brain bones, initially.
    Homo erectus had unusually thick dense femurs and unusually thick dense occiputs (rear skull bone), which counterbalanced the pace over orthogonal bipedal treks on the ground, substituting for the more typical long dense tail of other bipeds (T
    rex, giant short faced kangaroo, giant ground sloth, running jesus lizard). This primitive mechanical gyroscope was replaced by genetic software improvements enabling reduced body bone weight (esp. femur & occiput), faster & longer bipedal locomotion,
    drastically reduced climbing/brachiating abilities.

    Casually walking while chewing gum, chatting and carrying a squirming child is something only humans could ever do.
    @378 cm^3, S. tchadensis' braincase is similar to that of extant
    chimpanzees and approximately a third the size of modern human brains. >> >S chadensis was imo not a habitual nor obligate terrestrial orthograde biped, nor a part-time knucklewalking terrestrial quadruped, its foramen magnum reflected a more primitive arboreal orthograde bipedalism associated with suspensory slow
    brachiation x arboreal bipedalism, as in European miocene - pliocene apes and similar to but distinct from faster extant gibbons.

    Chimps & gorillas became more quadrupedal (partly pronograde terrestrial knucklewalking) while Homo became more bipedal (fully orthograde habitual obligate terrestrial striding), these produced changes of position and orientation of the foramen
    magnum.

    https://carta.anthropogeny.org/moca/topics/foramen-magnum-placement#:~:text=The%20foramen%20magnum%20position%20has,case%20for%20Ardipithecus%20and%20Sahelanthropus.
    The authors of the paper Erika cited disagree with your opinion.
    They might be right.


    If only there were some way to judge between contrasting opinions...

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Thu Oct 27 16:44:19 2022
    On Thursday, October 27, 2022 at 5:53:29 AM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 02:17:42 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 7:56:43 PM UTC-4, 69jp...@gmail.com wrote:
    On Wed, 26 Oct 2022 03:17:08 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 4:10:49 AM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 16:32:06 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, October 25, 2022 at 6:59:05 PM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 01:18:27 -0700, Trolidan7
    <Trol...@eternal-september.org> wrote:

    On 10/23/22 11:50 PM, jillery wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism: >> >> >> >>
    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    I tend to think of it as none of the above.

    Simply because it is not that easy to stand upright.

    When an animal stands upright you need to solve a problem -
    how do you keep from falling over forward and backward.

    This might seem simple but it is not because with a four
    footed animal the center of gravity forward and backward
    is between the front legs and the back legs, and often
    that is a greater distance than between the left legs and
    the right legs.
    Watch the cited videos. Erika points out the challenges of going from
    quadruped to biped, the differences between upright posture and
    bipedalism, and the plausibility of suspensory orthograde posture in
    trees as a precursor to bipedalism on the ground.
    Some animals that sort of walk on twos have not solved the
    problem - a kangaroo can hop but in general it can not
    stably stand. Either way, in essence, the long hand enables
    force to be supplied to the far front and far back to counter
    falling forward or backward - the forefoot and big toe are
    the front force appliers and the heel is the back force
    applier. Then of course there are some animals that might
    sort of walk on threes (I am thinking of the Jerboa) - but
    humans have an extra problem because they have no tail to
    possibly act as an extra walking limb, or at least a balance.
    That's why humans like big butts, I can not lie.

    Bigger butt bones, bigger brain bones, initially.
    Homo erectus had unusually thick dense femurs and unusually thick dense occiputs (rear skull bone), which counterbalanced the pace over orthogonal bipedal treks on the ground, substituting for the more typical long dense tail of other bipeds (T
    rex, giant short faced kangaroo, giant ground sloth, running jesus lizard). This primitive mechanical gyroscope was replaced by genetic software improvements enabling reduced body bone weight (esp. femur & occiput), faster & longer bipedal locomotion,
    drastically reduced climbing/brachiating abilities.

    Casually walking while chewing gum, chatting and carrying a squirming child is something only humans could ever do.
    @378 cm^3, S. tchadensis' braincase is similar to that of extant
    chimpanzees and approximately a third the size of modern human brains. >> >S chadensis was imo not a habitual nor obligate terrestrial orthograde biped, nor a part-time knucklewalking terrestrial quadruped, its foramen magnum reflected a more primitive arboreal orthograde bipedalism associated with suspensory slow
    brachiation x arboreal bipedalism, as in European miocene - pliocene apes and similar to but distinct from faster extant gibbons.

    Chimps & gorillas became more quadrupedal (partly pronograde terrestrial knucklewalking) while Homo became more bipedal (fully orthograde habitual obligate terrestrial striding), these produced changes of position and orientation of the foramen
    magnum.

    https://carta.anthropogeny.org/moca/topics/foramen-magnum-placement#:~:text=The%20foramen%20magnum%20position%20has,case%20for%20Ardipithecus%20and%20Sahelanthropus.
    The authors of the paper Erika cited disagree with your opinion.
    They might be right.
    If only there were some way to judge between contrasting opinions...

    Parsimony is good.
    Please direct me to the author(s) who disagree with what I wrote earlier. I don't know where to start, which vid, which paper... I'll examine inconsistencies (their or mine).
    DD

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Peter Nyikos@21:1/5 to 69jp...@gmail.com on Thu Oct 27 18:42:42 2022
    How about that! You, who seldom post here, actually did an on-topic OP.
    This puts you ahead of John Harshman: in the almost dozen years
    since I returned here, I don't recall him ever doing an on-topic OP to sci.bio.paleontology.
    This despite the fact that he has probably done a few thousand posts
    here in that time.

    I do have a few recommendations. The optimal place to post information about homini is sci.anthropology.paleo. Not only are they the "specialty" of that ng,
    it is more active, with more regulars than s.b.p. Best of all perhaps, Pandora takes a very active part there, going into depth with one person after another. Pandora occasionally posts to s.b.p. too, but the majority of her posts here are OP's.
    They are almost invariably excellent and thought-provoking, but she seldom comments on the thoughts she has provoked, even when they are on-topic
    in every sense of the word.

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:

    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis.

    I don't have enough time this evening to watch either this video or
    the one you mention below. This being a science ng, it is very
    appropriate to give the titles of these papers. Those of us who
    are interested in research papers shouldn't have to sit through a video
    to find out what they are.


    This fossil is remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    In science, hypotheses on such an open ended theme are seldom
    compelling. Before you decide to post this to s.a.p., I strongly recommend
    that you state this preferred hypothesis; some people there may already
    have heard of it (especially Pandora, who comes across as a professional
    well past the age of earning the Ph.D.) and have formulated ideas about it.


    Peter Nyikos
    Professor, Dept. of Mathematics -- standard disclaimer--
    University of South Carolina
    http://people.math.sc.edu/nyikos

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to peter2nyikos@gmail.com on Thu Oct 27 22:56:01 2022
    On Thu, 27 Oct 2022 18:42:42 -0700 (PDT), Peter Nyikos
    <peter2nyikos@gmail.com> wrote:

    How about that! You, who seldom post here, actually did an on-topic OP.
    This puts you ahead of John Harshman: in the almost dozen years
    since I returned here, I don't recall him ever doing an on-topic OP to sci.bio.paleontology.
    This despite the fact that he has probably done a few thousand posts
    here in that time.

    I do have a few recommendations. The optimal place to post information about >homini is sci.anthropology.paleo. Not only are they the "specialty" of that ng,
    it is more active, with more regulars than s.b.p. Best of all perhaps, Pandora >takes a very active part there, going into depth with one person after another.
    Pandora occasionally posts to s.b.p. too, but the majority of her posts here are OP's.
    They are almost invariably excellent and thought-provoking, but she seldom >comments on the thoughts she has provoked, even when they are on-topic
    in every sense of the word.

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:

    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Erika. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis.

    I don't have enough time this evening to watch either this video or
    the one you mention below. This being a science ng, it is very
    appropriate to give the titles of these papers. Those of us who
    are interested in research papers shouldn't have to sit through a video
    to find out what they are.


    This fossil is remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    In science, hypotheses on such an open ended theme are seldom
    compelling. Before you decide to post this to s.a.p., I strongly recommend >that you state this preferred hypothesis; some people there may already
    have heard of it (especially Pandora, who comes across as a professional
    well past the age of earning the Ph.D.) and have formulated ideas about it.


    The videos are comparable to college-level lectures. Anybody who is
    actually interested in the topic can easily find the answers to your
    questions in the cited videos. Anybody who is more interested in
    posting transparent obfuscating noise won't bother no matter what I
    post.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to daud.deden@gmail.com on Thu Oct 27 22:56:52 2022
    On Thu, 27 Oct 2022 16:44:19 -0700 (PDT), Daud Deden
    <daud.deden@gmail.com> wrote:

    On Thursday, October 27, 2022 at 5:53:29 AM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 02:17:42 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 7:56:43 PM UTC-4, 69jp...@gmail.com wrote:
    On Wed, 26 Oct 2022 03:17:08 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 4:10:49 AM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 16:32:06 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, October 25, 2022 at 6:59:05 PM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 01:18:27 -0700, Trolidan7
    <Trol...@eternal-september.org> wrote:

    On 10/23/22 11:50 PM, jillery wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Erika. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    I tend to think of it as none of the above.

    Simply because it is not that easy to stand upright.

    When an animal stands upright you need to solve a problem -
    how do you keep from falling over forward and backward.

    This might seem simple but it is not because with a four
    footed animal the center of gravity forward and backward
    is between the front legs and the back legs, and often
    that is a greater distance than between the left legs and
    the right legs.
    Watch the cited videos. Erika points out the challenges of going from
    quadruped to biped, the differences between upright posture and
    bipedalism, and the plausibility of suspensory orthograde posture in
    trees as a precursor to bipedalism on the ground.
    Some animals that sort of walk on twos have not solved the
    problem - a kangaroo can hop but in general it can not
    stably stand. Either way, in essence, the long hand enables
    force to be supplied to the far front and far back to counter
    falling forward or backward - the forefoot and big toe are
    the front force appliers and the heel is the back force
    applier. Then of course there are some animals that might
    sort of walk on threes (I am thinking of the Jerboa) - but
    humans have an extra problem because they have no tail to
    possibly act as an extra walking limb, or at least a balance.
    That's why humans like big butts, I can not lie.

    Bigger butt bones, bigger brain bones, initially.
    Homo erectus had unusually thick dense femurs and unusually thick dense occiputs (rear skull bone), which counterbalanced the pace over orthogonal bipedal treks on the ground, substituting for the more typical long dense tail of other bipeds (T
    rex, giant short faced kangaroo, giant ground sloth, running jesus lizard). This primitive mechanical gyroscope was replaced by genetic software improvements enabling reduced body bone weight (esp. femur & occiput), faster & longer bipedal locomotion,
    drastically reduced climbing/brachiating abilities.

    Casually walking while chewing gum, chatting and carrying a squirming child is something only humans could ever do.
    @378 cm^3, S. tchadensis' braincase is similar to that of extant
    chimpanzees and approximately a third the size of modern human brains.
    S chadensis was imo not a habitual nor obligate terrestrial orthograde biped, nor a part-time knucklewalking terrestrial quadruped, its foramen magnum reflected a more primitive arboreal orthograde bipedalism associated with suspensory slow
    brachiation x arboreal bipedalism, as in European miocene - pliocene apes and similar to but distinct from faster extant gibbons.

    Chimps & gorillas became more quadrupedal (partly pronograde terrestrial knucklewalking) while Homo became more bipedal (fully orthograde habitual obligate terrestrial striding), these produced changes of position and orientation of the foramen
    magnum.

    https://carta.anthropogeny.org/moca/topics/foramen-magnum-placement#:~:text=The%20foramen%20magnum%20position%20has,case%20for%20Ardipithecus%20and%20Sahelanthropus.
    The authors of the paper Erika cited disagree with your opinion.
    They might be right.
    If only there were some way to judge between contrasting opinions...

    Parsimony is good.
    Please direct me to the author(s) who disagree with what I wrote earlier. I don't know where to start, which vid, which paper... I'll examine inconsistencies (their or mine).


    Once again, watch the cited video. Erika identifies the paper in the
    first few minutes of the first vdeo. But if you watch/listen to all
    of both, you might actually learn something.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Peter Nyikos@21:1/5 to All on Thu Oct 27 19:26:00 2022
    On Tuesday, October 25, 2022 at 4:18:31 AM UTC-4, Trolidan7 wrote:
    On 10/23/22 11:50 PM, jillery wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    I tend to think of it as none of the above.

    Did you watch the video, to see what they were?

    Granted, with an open-ended subject like bipedalism, it is quite
    unlikely that any "why" that we humans can easily formulate
    gives a reason that is anywhere near complete. It's almost
    as bad as theories about how we developed such amazingly
    sophisticated speech. Simplified theories have been
    given derisive names like "bow-wow theory" and "ding-dong theory"
    or even been accused of being "pseudoscientific."

    Simply because it is not that easy to stand upright.

    When an animal stands upright you need to solve a problem -
    how do you keep from falling over forward and backward.

    This might seem simple but it is not because with a four
    footed animal the center of gravity forward and backward
    is between the front legs and the back legs, and often
    that is a greater distance than between the left legs and
    the right legs.

    Some animals that sort of walk on twos have not solved the
    problem - a kangaroo can hop but in general it can not
    stably stand.

    On the other hand, sifakas, the avahi, and the indri -- all lemurs -- are even more
    obligate bipedal than we are: their forelimbs are even shorter
    in proportion to their hindlimbs than ours are.

    Their primary way of getting from one place to another
    is fully bipedal hopping, generally between trees.
    However, I have a book with a photograph
    in which a sifaka has a very typically human style
    running pose, with arms swinging in opposite
    orientation to her wide-apart (from front to back) legs.


    Either way, in essence, the long hand enables
    force to be supplied to the far front and far back to counter
    falling forward or backward - the forefoot and big toe are
    the front force appliers and the heel is the back force
    applier. Then of course there are some animals that might
    sort of walk on threes (I am thinking of the Jerboa) - but
    humans have an extra problem because they have no tail to
    possibly act as an extra walking limb, or at least a balance.

    Indris have almost lost their tails, but you've made me wonder
    whether the long, narrow tail of that sifaka was an aid in
    balancing, making that human-like stride possible.


    Peter Nyikos
    Professor, Dept. of Mathematics -- standard disclaimer--
    Univ. of South Carolina at Columbia
    http://people.math.sc.edu/nyikos

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Thu Oct 27 21:13:31 2022
    On Thursday, October 27, 2022 at 10:56:53 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 16:44:19 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, October 27, 2022 at 5:53:29 AM UTC-4, 69jp...@gmail.com wrote: >> On Thu, 27 Oct 2022 02:17:42 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 7:56:43 PM UTC-4, 69jp...@gmail.com wrote:
    On Wed, 26 Oct 2022 03:17:08 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 4:10:49 AM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 16:32:06 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, October 25, 2022 at 6:59:05 PM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 01:18:27 -0700, Trolidan7
    <Trol...@eternal-september.org> wrote:

    On 10/23/22 11:50 PM, jillery wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Erika. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is >> >> >> >> >> remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    I tend to think of it as none of the above.

    Simply because it is not that easy to stand upright.

    When an animal stands upright you need to solve a problem -
    how do you keep from falling over forward and backward.

    This might seem simple but it is not because with a four
    footed animal the center of gravity forward and backward
    is between the front legs and the back legs, and often
    that is a greater distance than between the left legs and
    the right legs.
    Watch the cited videos. Erika points out the challenges of going from
    quadruped to biped, the differences between upright posture and >> >> >> >> bipedalism, and the plausibility of suspensory orthograde posture in
    trees as a precursor to bipedalism on the ground.
    Some animals that sort of walk on twos have not solved the
    problem - a kangaroo can hop but in general it can not
    stably stand. Either way, in essence, the long hand enables
    force to be supplied to the far front and far back to counter >> >> >> >> >falling forward or backward - the forefoot and big toe are
    the front force appliers and the heel is the back force
    applier. Then of course there are some animals that might
    sort of walk on threes (I am thinking of the Jerboa) - but
    humans have an extra problem because they have no tail to
    possibly act as an extra walking limb, or at least a balance. >> >> >> >> That's why humans like big butts, I can not lie.

    Bigger butt bones, bigger brain bones, initially.
    Homo erectus had unusually thick dense femurs and unusually thick dense occiputs (rear skull bone), which counterbalanced the pace over orthogonal bipedal treks on the ground, substituting for the more typical long dense tail of other bipeds (
    T rex, giant short faced kangaroo, giant ground sloth, running jesus lizard). This primitive mechanical gyroscope was replaced by genetic software improvements enabling reduced body bone weight (esp. femur & occiput), faster & longer bipedal locomotion,
    drastically reduced climbing/brachiating abilities.

    Casually walking while chewing gum, chatting and carrying a squirming child is something only humans could ever do.
    @378 cm^3, S. tchadensis' braincase is similar to that of extant
    chimpanzees and approximately a third the size of modern human brains.
    S chadensis was imo not a habitual nor obligate terrestrial orthograde biped, nor a part-time knucklewalking terrestrial quadruped, its foramen magnum reflected a more primitive arboreal orthograde bipedalism associated with suspensory slow
    brachiation x arboreal bipedalism, as in European miocene - pliocene apes and similar to but distinct from faster extant gibbons.

    Chimps & gorillas became more quadrupedal (partly pronograde terrestrial knucklewalking) while Homo became more bipedal (fully orthograde habitual obligate terrestrial striding), these produced changes of position and orientation of the foramen
    magnum.

    https://carta.anthropogeny.org/moca/topics/foramen-magnum-placement#:~:text=The%20foramen%20magnum%20position%20has,case%20for%20Ardipithecus%20and%20Sahelanthropus.
    The authors of the paper Erika cited disagree with your opinion.
    They might be right.
    If only there were some way to judge between contrasting opinions...

    Parsimony is good.
    Please direct me to the author(s) who disagree with what I wrote earlier. I don't know where to start, which vid, which paper... I'll examine inconsistencies (their or mine).
    Once again, watch the cited video. Erika identifies the paper in the
    first few minutes of the first vdeo. But if you watch/listen to all
    of both, you might actually learn something.
    Ok, I'd watched half of the 2nd video. I'll watch both tomorrow. I'll certainly learn something, I always do. For now, I stand behind every word I wrote earlier about Homo & Sahelanthropus.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to Daud Deden on Thu Oct 27 21:53:46 2022
    On Friday, October 28, 2022 at 12:20:59 AM UTC-4, Daud Deden wrote:
    On Friday, October 28, 2022 at 12:13:33 AM UTC-4, Daud Deden wrote:
    On Thursday, October 27, 2022 at 10:56:53 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 16:44:19 -0700 (PDT), Daud Deden <daud....@gmail.com> wrote:

    On Thursday, October 27, 2022 at 5:53:29 AM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 02:17:42 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 7:56:43 PM UTC-4, 69jp...@gmail.com wrote:
    On Wed, 26 Oct 2022 03:17:08 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 4:10:49 AM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 16:32:06 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, October 25, 2022 at 6:59:05 PM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 01:18:27 -0700, Trolidan7
    <Trol...@eternal-september.org> wrote:

    On 10/23/22 11:50 PM, jillery wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Erika. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    I tend to think of it as none of the above.

    Simply because it is not that easy to stand upright.

    When an animal stands upright you need to solve a problem - >> >> >> >> >how do you keep from falling over forward and backward.

    This might seem simple but it is not because with a four
    footed animal the center of gravity forward and backward
    is between the front legs and the back legs, and often
    that is a greater distance than between the left legs and >> >> >> >> >the right legs.
    Watch the cited videos. Erika points out the challenges of going from
    quadruped to biped, the differences between upright posture and
    bipedalism, and the plausibility of suspensory orthograde posture in
    trees as a precursor to bipedalism on the ground.
    Some animals that sort of walk on twos have not solved the >> >> >> >> >problem - a kangaroo can hop but in general it can not
    stably stand. Either way, in essence, the long hand enables >> >> >> >> >force to be supplied to the far front and far back to counter
    falling forward or backward - the forefoot and big toe are >> >> >> >> >the front force appliers and the heel is the back force
    applier. Then of course there are some animals that might >> >> >> >> >sort of walk on threes (I am thinking of the Jerboa) - but >> >> >> >> >humans have an extra problem because they have no tail to >> >> >> >> >possibly act as an extra walking limb, or at least a balance.
    That's why humans like big butts, I can not lie.

    Bigger butt bones, bigger brain bones, initially.
    Homo erectus had unusually thick dense femurs and unusually thick dense occiputs (rear skull bone), which counterbalanced the pace over orthogonal bipedal treks on the ground, substituting for the more typical long dense tail of other
    bipeds (T rex, giant short faced kangaroo, giant ground sloth, running jesus lizard). This primitive mechanical gyroscope was replaced by genetic software improvements enabling reduced body bone weight (esp. femur & occiput), faster & longer bipedal
    locomotion, drastically reduced climbing/brachiating abilities.

    Casually walking while chewing gum, chatting and carrying a squirming child is something only humans could ever do.
    @378 cm^3, S. tchadensis' braincase is similar to that of extant
    chimpanzees and approximately a third the size of modern human brains.
    S chadensis was imo not a habitual nor obligate terrestrial orthograde biped, nor a part-time knucklewalking terrestrial quadruped, its foramen magnum reflected a more primitive arboreal orthograde bipedalism associated with suspensory slow
    brachiation x arboreal bipedalism, as in European miocene - pliocene apes and similar to but distinct from faster extant gibbons.

    Chimps & gorillas became more quadrupedal (partly pronograde terrestrial knucklewalking) while Homo became more bipedal (fully orthograde habitual obligate terrestrial striding), these produced changes of position and orientation of the
    foramen magnum.

    https://carta.anthropogeny.org/moca/topics/foramen-magnum-placement#:~:text=The%20foramen%20magnum%20position%20has,case%20for%20Ardipithecus%20and%20Sahelanthropus.
    The authors of the paper Erika cited disagree with your opinion. >> >They might be right.
    If only there were some way to judge between contrasting opinions...

    Parsimony is good.
    Please direct me to the author(s) who disagree with what I wrote earlier. I don't know where to start, which vid, which paper... I'll examine inconsistencies (their or mine).
    Once again, watch the cited video. Erika identifies the paper in the first few minutes of the first vdeo. But if you watch/listen to all
    of both, you might actually learn something.
    Ok, I'd watched half of the 2nd video. I'll watch both tomorrow. I'll certainly learn something, I always do. For now, I stand behind every word I wrote earlier about Homo & Sahelanthropus.
    After a sneak peek, I see the paper, Postcranial ..., about the femur. I've skimmed it, no change in my thinking. But I'm flexible.
    I am so far sorely disappointed. At around 8:23, Erika intelligently but ignorantly describes the position of the foramen magnum and its significance. To her, bipedalism is terrestrial bipedalism. That is the central flaw in the study of hominoid,
    hominin & Homo evolution, one which I have already specifically addressed earlier. She and the various authors seem to be unable to comprehend the significance of arboreal habitual bipedalism. The authors do not disagree with my opinion, they are not
    even aware of the concept that bipedalism led to ape quadrupedalism. Erika is bright, but as blind as they are on this. More tomorrow, hopefully more enlightening.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to Daud Deden on Thu Oct 27 21:20:57 2022
    On Friday, October 28, 2022 at 12:13:33 AM UTC-4, Daud Deden wrote:
    On Thursday, October 27, 2022 at 10:56:53 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 16:44:19 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, October 27, 2022 at 5:53:29 AM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 02:17:42 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 7:56:43 PM UTC-4, 69jp...@gmail.com wrote:
    On Wed, 26 Oct 2022 03:17:08 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 4:10:49 AM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 16:32:06 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, October 25, 2022 at 6:59:05 PM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 01:18:27 -0700, Trolidan7
    <Trol...@eternal-september.org> wrote:

    On 10/23/22 11:50 PM, jillery wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Erika. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    I tend to think of it as none of the above.

    Simply because it is not that easy to stand upright.

    When an animal stands upright you need to solve a problem - >> >> >> >> >how do you keep from falling over forward and backward.

    This might seem simple but it is not because with a four
    footed animal the center of gravity forward and backward
    is between the front legs and the back legs, and often
    that is a greater distance than between the left legs and
    the right legs.
    Watch the cited videos. Erika points out the challenges of going from
    quadruped to biped, the differences between upright posture and
    bipedalism, and the plausibility of suspensory orthograde posture in
    trees as a precursor to bipedalism on the ground.
    Some animals that sort of walk on twos have not solved the
    problem - a kangaroo can hop but in general it can not
    stably stand. Either way, in essence, the long hand enables >> >> >> >> >force to be supplied to the far front and far back to counter >> >> >> >> >falling forward or backward - the forefoot and big toe are
    the front force appliers and the heel is the back force
    applier. Then of course there are some animals that might
    sort of walk on threes (I am thinking of the Jerboa) - but
    humans have an extra problem because they have no tail to
    possibly act as an extra walking limb, or at least a balance. >> >> >> >> That's why humans like big butts, I can not lie.

    Bigger butt bones, bigger brain bones, initially.
    Homo erectus had unusually thick dense femurs and unusually thick dense occiputs (rear skull bone), which counterbalanced the pace over orthogonal bipedal treks on the ground, substituting for the more typical long dense tail of other
    bipeds (T rex, giant short faced kangaroo, giant ground sloth, running jesus lizard). This primitive mechanical gyroscope was replaced by genetic software improvements enabling reduced body bone weight (esp. femur & occiput), faster & longer bipedal
    locomotion, drastically reduced climbing/brachiating abilities.

    Casually walking while chewing gum, chatting and carrying a squirming child is something only humans could ever do.
    @378 cm^3, S. tchadensis' braincase is similar to that of extant >> >> >> chimpanzees and approximately a third the size of modern human brains.
    S chadensis was imo not a habitual nor obligate terrestrial orthograde biped, nor a part-time knucklewalking terrestrial quadruped, its foramen magnum reflected a more primitive arboreal orthograde bipedalism associated with suspensory slow
    brachiation x arboreal bipedalism, as in European miocene - pliocene apes and similar to but distinct from faster extant gibbons.

    Chimps & gorillas became more quadrupedal (partly pronograde terrestrial knucklewalking) while Homo became more bipedal (fully orthograde habitual obligate terrestrial striding), these produced changes of position and orientation of the
    foramen magnum.

    https://carta.anthropogeny.org/moca/topics/foramen-magnum-placement#:~:text=The%20foramen%20magnum%20position%20has,case%20for%20Ardipithecus%20and%20Sahelanthropus.
    The authors of the paper Erika cited disagree with your opinion.
    They might be right.
    If only there were some way to judge between contrasting opinions...

    Parsimony is good.
    Please direct me to the author(s) who disagree with what I wrote earlier. I don't know where to start, which vid, which paper... I'll examine inconsistencies (their or mine).
    Once again, watch the cited video. Erika identifies the paper in the
    first few minutes of the first vdeo. But if you watch/listen to all
    of both, you might actually learn something.
    Ok, I'd watched half of the 2nd video. I'll watch both tomorrow. I'll certainly learn something, I always do. For now, I stand behind every word I wrote earlier about Homo & Sahelanthropus.
    After a sneak peek, I see the paper, Postcranial ..., about the femur. I've skimmed it, no change in my thinking. But I'm flexible.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to daud.deden@gmail.com on Fri Oct 28 04:45:54 2022
    On Thu, 27 Oct 2022 21:53:46 -0700 (PDT), Daud Deden
    <daud.deden@gmail.com> wrote:

    On Friday, October 28, 2022 at 12:20:59 AM UTC-4, Daud Deden wrote:
    On Friday, October 28, 2022 at 12:13:33 AM UTC-4, Daud Deden wrote:
    On Thursday, October 27, 2022 at 10:56:53 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 16:44:19 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, October 27, 2022 at 5:53:29 AM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 02:17:42 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 7:56:43 PM UTC-4, 69jp...@gmail.com wrote:
    On Wed, 26 Oct 2022 03:17:08 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 4:10:49 AM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 16:32:06 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, October 25, 2022 at 6:59:05 PM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 01:18:27 -0700, Trolidan7
    <Trol...@eternal-september.org> wrote:

    On 10/23/22 11:50 PM, jillery wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Erika. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism. >> > > >> >> >> >> >>
    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    I tend to think of it as none of the above.

    Simply because it is not that easy to stand upright.

    When an animal stands upright you need to solve a problem -
    how do you keep from falling over forward and backward.

    This might seem simple but it is not because with a four >> > > >> >> >> >> >footed animal the center of gravity forward and backward >> > > >> >> >> >> >is between the front legs and the back legs, and often
    that is a greater distance than between the left legs and >> > > >> >> >> >> >the right legs.
    Watch the cited videos. Erika points out the challenges of going from
    quadruped to biped, the differences between upright posture and
    bipedalism, and the plausibility of suspensory orthograde posture in
    trees as a precursor to bipedalism on the ground.
    Some animals that sort of walk on twos have not solved the >> > > >> >> >> >> >problem - a kangaroo can hop but in general it can not
    stably stand. Either way, in essence, the long hand enables
    force to be supplied to the far front and far back to counter
    falling forward or backward - the forefoot and big toe are >> > > >> >> >> >> >the front force appliers and the heel is the back force
    applier. Then of course there are some animals that might >> > > >> >> >> >> >sort of walk on threes (I am thinking of the Jerboa) - but >> > > >> >> >> >> >humans have an extra problem because they have no tail to >> > > >> >> >> >> >possibly act as an extra walking limb, or at least a balance.
    That's why humans like big butts, I can not lie.

    Bigger butt bones, bigger brain bones, initially.
    Homo erectus had unusually thick dense femurs and unusually thick dense occiputs (rear skull bone), which counterbalanced the pace over orthogonal bipedal treks on the ground, substituting for the more typical long dense tail of other
    bipeds (T rex, giant short faced kangaroo, giant ground sloth, running jesus lizard). This primitive mechanical gyroscope was replaced by genetic software improvements enabling reduced body bone weight (esp. femur & occiput), faster & longer bipedal
    locomotion, drastically reduced climbing/brachiating abilities.

    Casually walking while chewing gum, chatting and carrying a squirming child is something only humans could ever do.
    @378 cm^3, S. tchadensis' braincase is similar to that of extant
    chimpanzees and approximately a third the size of modern human brains.
    S chadensis was imo not a habitual nor obligate terrestrial orthograde biped, nor a part-time knucklewalking terrestrial quadruped, its foramen magnum reflected a more primitive arboreal orthograde bipedalism associated with suspensory slow
    brachiation x arboreal bipedalism, as in European miocene - pliocene apes and similar to but distinct from faster extant gibbons.

    Chimps & gorillas became more quadrupedal (partly pronograde terrestrial knucklewalking) while Homo became more bipedal (fully orthograde habitual obligate terrestrial striding), these produced changes of position and orientation of the
    foramen magnum.

    https://carta.anthropogeny.org/moca/topics/foramen-magnum-placement#:~:text=The%20foramen%20magnum%20position%20has,case%20for%20Ardipithecus%20and%20Sahelanthropus.
    The authors of the paper Erika cited disagree with your opinion. >> > > >> >They might be right.
    If only there were some way to judge between contrasting opinions... >> > > >
    Parsimony is good.
    Please direct me to the author(s) who disagree with what I wrote earlier. I don't know where to start, which vid, which paper... I'll examine inconsistencies (their or mine).
    Once again, watch the cited video. Erika identifies the paper in the
    first few minutes of the first vdeo. But if you watch/listen to all
    of both, you might actually learn something.
    Ok, I'd watched half of the 2nd video. I'll watch both tomorrow. I'll certainly learn something, I always do. For now, I stand behind every word I wrote earlier about Homo & Sahelanthropus.
    After a sneak peek, I see the paper, Postcranial ..., about the femur. I've skimmed it, no change in my thinking. But I'm flexible.
    I am so far sorely disappointed. At around 8:23, Erika intelligently but ignorantly describes the position of the foramen magnum and its significance. To her, bipedalism is terrestrial bipedalism. That is the central flaw in the study of hominoid,
    hominin & Homo evolution, one which I have already specifically addressed earlier. She and the various authors seem to be unable to comprehend the significance of arboreal habitual bipedalism. The authors do not disagree with my opinion, they are not
    even aware of the concept that bipedalism led to ape quadrupedalism. Erika is bright, but as blind as they are on this. More tomorrow, hopefully more enlightening.


    I acknowledge in the first video Erika mostly uses "bipedalism"
    without distinction between arboreal and terrestrial. However, her
    argument explicitly distinguishes between hominin and panin, and also explicitly mentions terrestrial bipedality once. My understanding is
    Erika uses hominin v panin to distinguish terrestrial v arboreal
    bipedalism. I could be wrong.

    Also, in the second video, Erika explicitly identifies arboreal
    bipedalism as an enabling adaptation to terrestrial bipedalism. So to
    say she doesn't comprehend its significance is an exaggeration at
    least.

    Erika is careful for copyright purposes to limit how much of the cited
    paper she includes in her video, so I can't say if the paper's authors
    make an explicit distinction between arboreal and terrestrial
    bipedalism. Someone who has access to the full paper will have to
    weigh in on that point.

    However, Erika does mention that the paper discusses anatomical
    features of the femur (proto linear aspira, gluteal tuberosity, calcar
    femoral {sp?}), and cortical bone of the ulnae. My understanding is
    these features are not present in arboreal bipedal species, and
    instead indicate the more robust musculature of terrestrial
    bipedalism.

    Finally, Erika's expressed reservation with the paper is if the
    evidence supports habitual bipedalism. She argues that would inform
    whether the common ancestor between hominin and panin was more
    human-like or more chimpanzee-like.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Fri Oct 28 14:45:08 2022
    On Friday, October 28, 2022 at 4:45:58 AM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 21:53:46 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, October 28, 2022 at 12:20:59 AM UTC-4, Daud Deden wrote:
    On Friday, October 28, 2022 at 12:13:33 AM UTC-4, Daud Deden wrote:
    On Thursday, October 27, 2022 at 10:56:53 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 16:44:19 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, October 27, 2022 at 5:53:29 AM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 02:17:42 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 7:56:43 PM UTC-4, 69jp...@gmail.com wrote:
    On Wed, 26 Oct 2022 03:17:08 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 4:10:49 AM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 16:32:06 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, October 25, 2022 at 6:59:05 PM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 01:18:27 -0700, Trolidan7
    <Trol...@eternal-september.org> wrote:

    On 10/23/22 11:50 PM, jillery wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Erika. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism. >> > > >> >> >> >> >>
    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    I tend to think of it as none of the above.

    Simply because it is not that easy to stand upright.

    When an animal stands upright you need to solve a problem -
    how do you keep from falling over forward and backward. >> > > >> >> >> >> >
    This might seem simple but it is not because with a four >> > > >> >> >> >> >footed animal the center of gravity forward and backward >> > > >> >> >> >> >is between the front legs and the back legs, and often >> > > >> >> >> >> >that is a greater distance than between the left legs and
    the right legs.
    Watch the cited videos. Erika points out the challenges of going from
    quadruped to biped, the differences between upright posture and
    bipedalism, and the plausibility of suspensory orthograde posture in
    trees as a precursor to bipedalism on the ground.
    Some animals that sort of walk on twos have not solved the
    problem - a kangaroo can hop but in general it can not >> > > >> >> >> >> >stably stand. Either way, in essence, the long hand enables
    force to be supplied to the far front and far back to counter
    falling forward or backward - the forefoot and big toe are
    the front force appliers and the heel is the back force >> > > >> >> >> >> >applier. Then of course there are some animals that might
    sort of walk on threes (I am thinking of the Jerboa) - but
    humans have an extra problem because they have no tail to
    possibly act as an extra walking limb, or at least a balance.
    That's why humans like big butts, I can not lie.

    Bigger butt bones, bigger brain bones, initially.
    Homo erectus had unusually thick dense femurs and unusually thick dense occiputs (rear skull bone), which counterbalanced the pace over orthogonal bipedal treks on the ground, substituting for the more typical long dense tail of other
    bipeds (T rex, giant short faced kangaroo, giant ground sloth, running jesus lizard). This primitive mechanical gyroscope was replaced by genetic software improvements enabling reduced body bone weight (esp. femur & occiput), faster & longer bipedal
    locomotion, drastically reduced climbing/brachiating abilities.

    Casually walking while chewing gum, chatting and carrying a squirming child is something only humans could ever do.
    @378 cm^3, S. tchadensis' braincase is similar to that of extant
    chimpanzees and approximately a third the size of modern human brains.
    S chadensis was imo not a habitual nor obligate terrestrial orthograde biped, nor a part-time knucklewalking terrestrial quadruped, its foramen magnum reflected a more primitive arboreal orthograde bipedalism associated with suspensory
    slow brachiation x arboreal bipedalism, as in European miocene - pliocene apes and similar to but distinct from faster extant gibbons.

    Chimps & gorillas became more quadrupedal (partly pronograde terrestrial knucklewalking) while Homo became more bipedal (fully orthograde habitual obligate terrestrial striding), these produced changes of position and orientation of the
    foramen magnum.

    https://carta.anthropogeny.org/moca/topics/foramen-magnum-placement#:~:text=The%20foramen%20magnum%20position%20has,case%20for%20Ardipithecus%20and%20Sahelanthropus.
    The authors of the paper Erika cited disagree with your opinion.
    They might be right.
    If only there were some way to judge between contrasting opinions...

    Parsimony is good.
    Please direct me to the author(s) who disagree with what I wrote earlier. I don't know where to start, which vid, which paper... I'll examine inconsistencies (their or mine).
    Once again, watch the cited video. Erika identifies the paper in the >> > > first few minutes of the first vdeo. But if you watch/listen to all >> > > of both, you might actually learn something.
    Ok, I'd watched half of the 2nd video. I'll watch both tomorrow. I'll certainly learn something, I always do. For now, I stand behind every word I wrote earlier about Homo & Sahelanthropus.
    After a sneak peek, I see the paper, Postcranial ..., about the femur. I've skimmed it, no change in my thinking. But I'm flexible.
    I am so far sorely disappointed. At around 8:23, Erika intelligently but ignorantly describes the position of the foramen magnum and its significance. To her, bipedalism is terrestrial bipedalism. That is the central flaw in the study of hominoid,
    hominin & Homo evolution, one which I have already specifically addressed earlier. She and the various authors seem to be unable to comprehend the significance of arboreal habitual bipedalism. The authors do not disagree with my opinion, they are not
    even aware of the concept that bipedalism led to ape quadrupedalism. Erika is bright, but as blind as they are on this. More tomorrow, hopefully more enlightening.
    I acknowledge in the first video Erika mostly uses "bipedalism"
    without distinction between arboreal and terrestrial. However, her
    argument explicitly distinguishes between hominin and panin, and also explicitly mentions terrestrial bipedality once. My understanding is
    Erika uses hominin v panin to distinguish terrestrial v arboreal
    bipedalism. I could be wrong.

    Also, in the second video, Erika explicitly identifies arboreal
    bipedalism as an enabling adaptation to terrestrial bipedalism. So to
    say she doesn't comprehend its significance is an exaggeration at
    least.

    Erika is careful for copyright purposes to limit how much of the cited
    paper she includes in her video, so I can't say if the paper's authors
    make an explicit distinction between arboreal and terrestrial
    bipedalism. Someone who has access to the full paper will have to
    weigh in on that point.

    However, Erika does mention that the paper discusses anatomical
    features of the femur (proto linear aspira, gluteal tuberosity, calcar femoral {sp?}), and cortical bone of the ulnae. My understanding is
    these features are not present in arboreal bipedal species, and
    instead indicate the more robust musculature of terrestrial
    bipedalism.

    Finally, Erika's expressed reservation with the paper is if the
    evidence supports habitual bipedalism. She argues that would inform
    whether the common ancestor between hominin and panin was more
    human-like or more chimpanzee-like.

    My written response was lost. Damn. 15 sentences evaporated.
    The data graphs have nothing about hylobatids or macaques, so are worthless. Near the end of video one, Erika talks about 'bipedal or arboreal', revealing that she still doesn't get it.
    J: "these features are not present in arboreal bipedal species" Extant knucklewalking apes which sleep in bowl nests? Humans are gracile terrestrial bipeds.
    Not even mentioned: gibbons and humans share long achilles tendon and long lower back, opposite of extant great apes.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to Daud Deden on Fri Oct 28 21:26:43 2022
    On Friday, October 28, 2022 at 5:45:10 PM UTC-4, Daud Deden wrote:
    On Friday, October 28, 2022 at 4:45:58 AM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 21:53:46 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, October 28, 2022 at 12:20:59 AM UTC-4, Daud Deden wrote:
    On Friday, October 28, 2022 at 12:13:33 AM UTC-4, Daud Deden wrote:
    On Thursday, October 27, 2022 at 10:56:53 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 16:44:19 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, October 27, 2022 at 5:53:29 AM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 02:17:42 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 7:56:43 PM UTC-4, 69jp...@gmail.com wrote:
    On Wed, 26 Oct 2022 03:17:08 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 4:10:49 AM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 16:32:06 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, October 25, 2022 at 6:59:05 PM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 01:18:27 -0700, Trolidan7
    <Trol...@eternal-september.org> wrote:

    On 10/23/22 11:50 PM, jillery wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Erika. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    I tend to think of it as none of the above.

    Simply because it is not that easy to stand upright. >> > > >> >> >> >> >
    When an animal stands upright you need to solve a problem -
    how do you keep from falling over forward and backward.

    This might seem simple but it is not because with a four
    footed animal the center of gravity forward and backward
    is between the front legs and the back legs, and often >> > > >> >> >> >> >that is a greater distance than between the left legs and
    the right legs.
    Watch the cited videos. Erika points out the challenges of going from
    quadruped to biped, the differences between upright posture and
    bipedalism, and the plausibility of suspensory orthograde posture in
    trees as a precursor to bipedalism on the ground.
    Some animals that sort of walk on twos have not solved the
    problem - a kangaroo can hop but in general it can not >> > > >> >> >> >> >stably stand. Either way, in essence, the long hand enables
    force to be supplied to the far front and far back to counter
    falling forward or backward - the forefoot and big toe are
    the front force appliers and the heel is the back force
    applier. Then of course there are some animals that might
    sort of walk on threes (I am thinking of the Jerboa) - but
    humans have an extra problem because they have no tail to
    possibly act as an extra walking limb, or at least a balance.
    That's why humans like big butts, I can not lie.

    Bigger butt bones, bigger brain bones, initially.
    Homo erectus had unusually thick dense femurs and unusually thick dense occiputs (rear skull bone), which counterbalanced the pace over orthogonal bipedal treks on the ground, substituting for the more typical long dense tail of
    other bipeds (T rex, giant short faced kangaroo, giant ground sloth, running jesus lizard). This primitive mechanical gyroscope was replaced by genetic software improvements enabling reduced body bone weight (esp. femur & occiput), faster & longer
    bipedal locomotion, drastically reduced climbing/brachiating abilities.

    Casually walking while chewing gum, chatting and carrying a squirming child is something only humans could ever do.
    @378 cm^3, S. tchadensis' braincase is similar to that of extant
    chimpanzees and approximately a third the size of modern human brains.
    S chadensis was imo not a habitual nor obligate terrestrial orthograde biped, nor a part-time knucklewalking terrestrial quadruped, its foramen magnum reflected a more primitive arboreal orthograde bipedalism associated with suspensory
    slow brachiation x arboreal bipedalism, as in European miocene - pliocene apes and similar to but distinct from faster extant gibbons.

    Chimps & gorillas became more quadrupedal (partly pronograde terrestrial knucklewalking) while Homo became more bipedal (fully orthograde habitual obligate terrestrial striding), these produced changes of position and orientation of the
    foramen magnum.

    https://carta.anthropogeny.org/moca/topics/foramen-magnum-placement#:~:text=The%20foramen%20magnum%20position%20has,case%20for%20Ardipithecus%20and%20Sahelanthropus.
    The authors of the paper Erika cited disagree with your opinion.
    They might be right.
    If only there were some way to judge between contrasting opinions...

    Parsimony is good.
    Please direct me to the author(s) who disagree with what I wrote earlier. I don't know where to start, which vid, which paper... I'll examine inconsistencies (their or mine).
    Once again, watch the cited video. Erika identifies the paper in the
    first few minutes of the first vdeo. But if you watch/listen to all >> > > of both, you might actually learn something.
    Ok, I'd watched half of the 2nd video. I'll watch both tomorrow. I'll certainly learn something, I always do. For now, I stand behind every word I wrote earlier about Homo & Sahelanthropus.
    After a sneak peek, I see the paper, Postcranial ..., about the femur. I've skimmed it, no change in my thinking. But I'm flexible.
    I am so far sorely disappointed. At around 8:23, Erika intelligently but ignorantly describes the position of the foramen magnum and its significance. To her, bipedalism is terrestrial bipedalism. That is the central flaw in the study of hominoid,
    hominin & Homo evolution, one which I have already specifically addressed earlier. She and the various authors seem to be unable to comprehend the significance of arboreal habitual bipedalism. The authors do not disagree with my opinion, they are not
    even aware of the concept that bipedalism led to ape quadrupedalism. Erika is bright, but as blind as they are on this. More tomorrow, hopefully more enlightening.
    I acknowledge in the first video Erika mostly uses "bipedalism"
    without distinction between arboreal and terrestrial. However, her argument explicitly distinguishes between hominin and panin, and also explicitly mentions terrestrial bipedality once. My understanding is
    Erika uses hominin v panin to distinguish terrestrial v arboreal bipedalism. I could be wrong.

    Also, in the second video, Erika explicitly identifies arboreal
    bipedalism as an enabling adaptation to terrestrial bipedalism. So to
    say she doesn't comprehend its significance is an exaggeration at
    least.

    Erika is careful for copyright purposes to limit how much of the cited paper she includes in her video, so I can't say if the paper's authors make an explicit distinction between arboreal and terrestrial
    bipedalism. Someone who has access to the full paper will have to
    weigh in on that point.

    However, Erika does mention that the paper discusses anatomical
    features of the femur (proto linear aspira, gluteal tuberosity, calcar femoral {sp?}), and cortical bone of the ulnae. My understanding is
    these features are not present in arboreal bipedal species, and
    instead indicate the more robust musculature of terrestrial
    bipedalism.

    Finally, Erika's expressed reservation with the paper is if the
    evidence supports habitual bipedalism. She argues that would inform whether the common ancestor between hominin and panin was more
    human-like or more chimpanzee-like.
    My written response was lost. Damn. 15 sentences evaporated.
    The data graphs have nothing about hylobatids or macaques, so are worthless. Near the end of video one, Erika talks about 'bipedal or arboreal', revealing that she still doesn't get it.
    J: "these features are not present in arboreal bipedal species" Extant knucklewalking apes which sleep in bowl nests? Humans are gracile terrestrial bipeds.
    Not even mentioned: gibbons and humans share long achilles tendon and long lower back, opposite of extant great apes.
    There's also this: https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-022-08828-7

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to daud.deden@gmail.com on Sat Oct 29 02:11:41 2022
    On Fri, 28 Oct 2022 21:26:43 -0700 (PDT), Daud Deden
    <daud.deden@gmail.com> wrote:

    On Friday, October 28, 2022 at 5:45:10 PM UTC-4, Daud Deden wrote:
    On Friday, October 28, 2022 at 4:45:58 AM UTC-4, 69jp...@gmail.com wrote: >> > On Thu, 27 Oct 2022 21:53:46 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, October 28, 2022 at 12:20:59 AM UTC-4, Daud Deden wrote:
    On Friday, October 28, 2022 at 12:13:33 AM UTC-4, Daud Deden wrote:
    On Thursday, October 27, 2022 at 10:56:53 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 16:44:19 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, October 27, 2022 at 5:53:29 AM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 02:17:42 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 7:56:43 PM UTC-4, 69jp...@gmail.com wrote:
    On Wed, 26 Oct 2022 03:17:08 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 4:10:49 AM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 16:32:06 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, October 25, 2022 at 6:59:05 PM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 01:18:27 -0700, Trolidan7
    <Trol...@eternal-september.org> wrote:

    On 10/23/22 11:50 PM, jillery wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Erika. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    I tend to think of it as none of the above.

    Simply because it is not that easy to stand upright. >> > >> > > >> >> >> >> >
    When an animal stands upright you need to solve a problem -
    how do you keep from falling over forward and backward.

    This might seem simple but it is not because with a four
    footed animal the center of gravity forward and backward
    is between the front legs and the back legs, and often
    that is a greater distance than between the left legs and
    the right legs.
    Watch the cited videos. Erika points out the challenges of going from
    quadruped to biped, the differences between upright posture and
    bipedalism, and the plausibility of suspensory orthograde posture in
    trees as a precursor to bipedalism on the ground.
    Some animals that sort of walk on twos have not solved the
    problem - a kangaroo can hop but in general it can not
    stably stand. Either way, in essence, the long hand enables
    force to be supplied to the far front and far back to counter
    falling forward or backward - the forefoot and big toe are
    the front force appliers and the heel is the back force
    applier. Then of course there are some animals that might
    sort of walk on threes (I am thinking of the Jerboa) - but
    humans have an extra problem because they have no tail to
    possibly act as an extra walking limb, or at least a balance.
    That's why humans like big butts, I can not lie.

    Bigger butt bones, bigger brain bones, initially.
    Homo erectus had unusually thick dense femurs and unusually thick dense occiputs (rear skull bone), which counterbalanced the pace over orthogonal bipedal treks on the ground, substituting for the more typical long dense tail of
    other bipeds (T rex, giant short faced kangaroo, giant ground sloth, running jesus lizard). This primitive mechanical gyroscope was replaced by genetic software improvements enabling reduced body bone weight (esp. femur & occiput), faster & longer
    bipedal locomotion, drastically reduced climbing/brachiating abilities.

    Casually walking while chewing gum, chatting and carrying a squirming child is something only humans could ever do.
    @378 cm^3, S. tchadensis' braincase is similar to that of extant
    chimpanzees and approximately a third the size of modern human brains.
    S chadensis was imo not a habitual nor obligate terrestrial orthograde biped, nor a part-time knucklewalking terrestrial quadruped, its foramen magnum reflected a more primitive arboreal orthograde bipedalism associated with suspensory
    slow brachiation x arboreal bipedalism, as in European miocene - pliocene apes and similar to but distinct from faster extant gibbons.

    Chimps & gorillas became more quadrupedal (partly pronograde terrestrial knucklewalking) while Homo became more bipedal (fully orthograde habitual obligate terrestrial striding), these produced changes of position and orientation of
    the foramen magnum.

    https://carta.anthropogeny.org/moca/topics/foramen-magnum-placement#:~:text=The%20foramen%20magnum%20position%20has,case%20for%20Ardipithecus%20and%20Sahelanthropus.
    The authors of the paper Erika cited disagree with your opinion.
    They might be right.
    If only there were some way to judge between contrasting opinions...

    Parsimony is good.
    Please direct me to the author(s) who disagree with what I wrote earlier. I don't know where to start, which vid, which paper... I'll examine inconsistencies (their or mine).
    Once again, watch the cited video. Erika identifies the paper in the
    first few minutes of the first vdeo. But if you watch/listen to all
    of both, you might actually learn something.
    Ok, I'd watched half of the 2nd video. I'll watch both tomorrow. I'll certainly learn something, I always do. For now, I stand behind every word I wrote earlier about Homo & Sahelanthropus.
    After a sneak peek, I see the paper, Postcranial ..., about the femur. I've skimmed it, no change in my thinking. But I'm flexible.
    I am so far sorely disappointed. At around 8:23, Erika intelligently but ignorantly describes the position of the foramen magnum and its significance. To her, bipedalism is terrestrial bipedalism. That is the central flaw in the study of hominoid,
    hominin & Homo evolution, one which I have already specifically addressed earlier. She and the various authors seem to be unable to comprehend the significance of arboreal habitual bipedalism. The authors do not disagree with my opinion, they are not
    even aware of the concept that bipedalism led to ape quadrupedalism. Erika is bright, but as blind as they are on this. More tomorrow, hopefully more enlightening.
    I acknowledge in the first video Erika mostly uses "bipedalism"
    without distinction between arboreal and terrestrial. However, her
    argument explicitly distinguishes between hominin and panin, and also
    explicitly mentions terrestrial bipedality once. My understanding is
    Erika uses hominin v panin to distinguish terrestrial v arboreal
    bipedalism. I could be wrong.

    Also, in the second video, Erika explicitly identifies arboreal
    bipedalism as an enabling adaptation to terrestrial bipedalism. So to
    say she doesn't comprehend its significance is an exaggeration at
    least.

    Erika is careful for copyright purposes to limit how much of the cited
    paper she includes in her video, so I can't say if the paper's authors
    make an explicit distinction between arboreal and terrestrial
    bipedalism. Someone who has access to the full paper will have to
    weigh in on that point.

    However, Erika does mention that the paper discusses anatomical
    features of the femur (proto linear aspira, gluteal tuberosity, calcar
    femoral {sp?}), and cortical bone of the ulnae. My understanding is
    these features are not present in arboreal bipedal species, and
    instead indicate the more robust musculature of terrestrial
    bipedalism.

    Finally, Erika's expressed reservation with the paper is if the
    evidence supports habitual bipedalism. She argues that would inform
    whether the common ancestor between hominin and panin was more
    human-like or more chimpanzee-like.
    My written response was lost. Damn. 15 sentences evaporated.


    Been there, done that. I agree it suks.


    The data graphs have nothing about hylobatids or macaques, so are worthless.
    Near the end of video one, Erika talks about 'bipedal or arboreal', revealing that she still doesn't get it.
    J: "these features are not present in arboreal bipedal species"


    I can't find where Erika says that, but I suspect she's referring to
    the 4 anatomical features of the tibia and ulnae I mention above. What
    arboreal bipedal species do you know with these features?


    Extant knucklewalking apes which sleep in bowl nests? Humans are gracile terrestrial bipeds.
    Not even mentioned: gibbons and humans share long achilles tendon and long lower back, opposite of extant great apes.


    Do the cited papers mention these things? If not, that would explain
    why Erika doesn't either.


    There's also this: https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-022-08828-7


    Not sure what chromosome 2 fusion has to do with this topic. Please
    elaborate.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Sat Oct 29 05:26:51 2022
    On Saturday, October 29, 2022 at 2:11:43 AM UTC-4, 69jp...@gmail.com wrote:
    On Fri, 28 Oct 2022 21:26:43 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, October 28, 2022 at 5:45:10 PM UTC-4, Daud Deden wrote:
    On Friday, October 28, 2022 at 4:45:58 AM UTC-4, 69jp...@gmail.com wrote: >> > On Thu, 27 Oct 2022 21:53:46 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, October 28, 2022 at 12:20:59 AM UTC-4, Daud Deden wrote:
    On Friday, October 28, 2022 at 12:13:33 AM UTC-4, Daud Deden wrote: >> > >> > On Thursday, October 27, 2022 at 10:56:53 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 16:44:19 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, October 27, 2022 at 5:53:29 AM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 02:17:42 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 7:56:43 PM UTC-4, 69jp...@gmail.com wrote:
    On Wed, 26 Oct 2022 03:17:08 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 4:10:49 AM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 16:32:06 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, October 25, 2022 at 6:59:05 PM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 01:18:27 -0700, Trolidan7
    <Trol...@eternal-september.org> wrote:

    On 10/23/22 11:50 PM, jillery wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Erika. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    I tend to think of it as none of the above.

    Simply because it is not that easy to stand upright.

    When an animal stands upright you need to solve a problem -
    how do you keep from falling over forward and backward.

    This might seem simple but it is not because with a four
    footed animal the center of gravity forward and backward
    is between the front legs and the back legs, and often
    that is a greater distance than between the left legs and
    the right legs.
    Watch the cited videos. Erika points out the challenges of going from
    quadruped to biped, the differences between upright posture and
    bipedalism, and the plausibility of suspensory orthograde posture in
    trees as a precursor to bipedalism on the ground.
    Some animals that sort of walk on twos have not solved the
    problem - a kangaroo can hop but in general it can not
    stably stand. Either way, in essence, the long hand enables
    force to be supplied to the far front and far back to counter
    falling forward or backward - the forefoot and big toe are
    the front force appliers and the heel is the back force
    applier. Then of course there are some animals that might
    sort of walk on threes (I am thinking of the Jerboa) - but
    humans have an extra problem because they have no tail to
    possibly act as an extra walking limb, or at least a balance.
    That's why humans like big butts, I can not lie.

    Bigger butt bones, bigger brain bones, initially.
    Homo erectus had unusually thick dense femurs and unusually thick dense occiputs (rear skull bone), which counterbalanced the pace over orthogonal bipedal treks on the ground, substituting for the more typical long dense tail of
    other bipeds (T rex, giant short faced kangaroo, giant ground sloth, running jesus lizard). This primitive mechanical gyroscope was replaced by genetic software improvements enabling reduced body bone weight (esp. femur & occiput), faster & longer
    bipedal locomotion, drastically reduced climbing/brachiating abilities.

    Casually walking while chewing gum, chatting and carrying a squirming child is something only humans could ever do.
    @378 cm^3, S. tchadensis' braincase is similar to that of extant
    chimpanzees and approximately a third the size of modern human brains.
    S chadensis was imo not a habitual nor obligate terrestrial orthograde biped, nor a part-time knucklewalking terrestrial quadruped, its foramen magnum reflected a more primitive arboreal orthograde bipedalism associated with
    suspensory slow brachiation x arboreal bipedalism, as in European miocene - pliocene apes and similar to but distinct from faster extant gibbons.

    Chimps & gorillas became more quadrupedal (partly pronograde terrestrial knucklewalking) while Homo became more bipedal (fully orthograde habitual obligate terrestrial striding), these produced changes of position and orientation of
    the foramen magnum.

    https://carta.anthropogeny.org/moca/topics/foramen-magnum-placement#:~:text=The%20foramen%20magnum%20position%20has,case%20for%20Ardipithecus%20and%20Sahelanthropus.
    The authors of the paper Erika cited disagree with your opinion.
    They might be right.
    If only there were some way to judge between contrasting opinions...

    Parsimony is good.
    Please direct me to the author(s) who disagree with what I wrote earlier. I don't know where to start, which vid, which paper... I'll examine inconsistencies (their or mine).
    Once again, watch the cited video. Erika identifies the paper in the
    first few minutes of the first vdeo. But if you watch/listen to all
    of both, you might actually learn something.
    Ok, I'd watched half of the 2nd video. I'll watch both tomorrow. I'll certainly learn something, I always do. For now, I stand behind every word I wrote earlier about Homo & Sahelanthropus.
    After a sneak peek, I see the paper, Postcranial ..., about the femur. I've skimmed it, no change in my thinking. But I'm flexible.
    I am so far sorely disappointed. At around 8:23, Erika intelligently but ignorantly describes the position of the foramen magnum and its significance. To her, bipedalism is terrestrial bipedalism. That is the central flaw in the study of hominoid,
    hominin & Homo evolution, one which I have already specifically addressed earlier. She and the various authors seem to be unable to comprehend the significance of arboreal habitual bipedalism. The authors do not disagree with my opinion, they are not
    even aware of the concept that bipedalism led to ape quadrupedalism. Erika is bright, but as blind as they are on this. More tomorrow, hopefully more enlightening.
    I acknowledge in the first video Erika mostly uses "bipedalism"
    without distinction between arboreal and terrestrial. However, her
    argument explicitly distinguishes between hominin and panin, and also >> > explicitly mentions terrestrial bipedality once. My understanding is
    Erika uses hominin v panin to distinguish terrestrial v arboreal
    bipedalism. I could be wrong.

    Also, in the second video, Erika explicitly identifies arboreal
    bipedalism as an enabling adaptation to terrestrial bipedalism. So to >> > say she doesn't comprehend its significance is an exaggeration at
    least.

    Erika is careful for copyright purposes to limit how much of the cited >> > paper she includes in her video, so I can't say if the paper's authors >> > make an explicit distinction between arboreal and terrestrial
    bipedalism. Someone who has access to the full paper will have to
    weigh in on that point.

    However, Erika does mention that the paper discusses anatomical
    features of the femur (proto linear aspira, gluteal tuberosity, calcar >> > femoral {sp?}), and cortical bone of the ulnae. My understanding is
    these features are not present in arboreal bipedal species, and
    instead indicate the more robust musculature of terrestrial
    bipedalism.

    Finally, Erika's expressed reservation with the paper is if the
    evidence supports habitual bipedalism. She argues that would inform
    whether the common ancestor between hominin and panin was more
    human-like or more chimpanzee-like.
    My written response was lost. Damn. 15 sentences evaporated.
    Been there, done that. I agree it suks.
    The data graphs have nothing about hylobatids or macaques, so are worthless.
    Near the end of video one, Erika talks about 'bipedal or arboreal', revealing that she still doesn't get it.
    J: "these features are not present in arboreal bipedal species"
    I can't find where Erika says that,

    Possibly video 2.

    but I suspect she's referring to
    the 4 anatomical features of the tibia [femur] and ulnae I mention above. What
    arboreal bipedal species do you know with these features?

    All, in a spectrum, Homo at one end, arboreals the other.

    Extant knucklewalking apes which sleep in bowl nests? Humans are gracile terrestrial bipeds.
    Not even mentioned: gibbons and humans share long achilles tendon and long lower back, opposite of extant great apes.
    Do the cited papers mention these things? If not, that would explain
    why Erika doesn't either.

    *Human bipedalism* cannot be *explained* without it. (It can be discussed & lectured, but not explained.) Picking out a few unique features and ignoring others doesn't explain anything.

    There's also this: https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-022-08828-7
    Not sure what chromosome 2 fusion has to do with this topic. Please elaborate.
    H/P split estimated timing .9ma is much later than MSC (Medit. & Red Sea dried out); H erectus bridged the est. date, so would have had 24, not 23 like Hs. I doubt their estimate.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to daud.deden@gmail.com on Sun Oct 30 02:40:43 2022
    On Sat, 29 Oct 2022 05:26:51 -0700 (PDT), Daud Deden
    <daud.deden@gmail.com> wrote:

    On Saturday, October 29, 2022 at 2:11:43 AM UTC-4, 69jp...@gmail.com wrote:
    On Fri, 28 Oct 2022 21:26:43 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, October 28, 2022 at 5:45:10 PM UTC-4, Daud Deden wrote:
    On Friday, October 28, 2022 at 4:45:58 AM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 21:53:46 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, October 28, 2022 at 12:20:59 AM UTC-4, Daud Deden wrote: >> >> > >> On Friday, October 28, 2022 at 12:13:33 AM UTC-4, Daud Deden wrote: >> >> > >> > On Thursday, October 27, 2022 at 10:56:53 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 16:44:19 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, October 27, 2022 at 5:53:29 AM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 02:17:42 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 7:56:43 PM UTC-4, 69jp...@gmail.com wrote:
    On Wed, 26 Oct 2022 03:17:08 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 4:10:49 AM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 16:32:06 -0700 (PDT), Daud Deden >> >> > >> > > >> >> >> <daud....@gmail.com> wrote:

    On Tuesday, October 25, 2022 at 6:59:05 PM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 01:18:27 -0700, Trolidan7
    <Trol...@eternal-september.org> wrote:

    On 10/23/22 11:50 PM, jillery wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Erika. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    I tend to think of it as none of the above.

    Simply because it is not that easy to stand upright.

    When an animal stands upright you need to solve a problem -
    how do you keep from falling over forward and backward.

    This might seem simple but it is not because with a four
    footed animal the center of gravity forward and backward
    is between the front legs and the back legs, and often
    that is a greater distance than between the left legs and
    the right legs.
    Watch the cited videos. Erika points out the challenges of going from
    quadruped to biped, the differences between upright posture and
    bipedalism, and the plausibility of suspensory orthograde posture in
    trees as a precursor to bipedalism on the ground. >> >> > >> > > >> >> >> >> >Some animals that sort of walk on twos have not solved the
    problem - a kangaroo can hop but in general it can not
    stably stand. Either way, in essence, the long hand enables
    force to be supplied to the far front and far back to counter
    falling forward or backward - the forefoot and big toe are
    the front force appliers and the heel is the back force
    applier. Then of course there are some animals that might
    sort of walk on threes (I am thinking of the Jerboa) - but
    humans have an extra problem because they have no tail to
    possibly act as an extra walking limb, or at least a balance.
    That's why humans like big butts, I can not lie.

    Bigger butt bones, bigger brain bones, initially.
    Homo erectus had unusually thick dense femurs and unusually thick dense occiputs (rear skull bone), which counterbalanced the pace over orthogonal bipedal treks on the ground, substituting for the more typical long dense tail of
    other bipeds (T rex, giant short faced kangaroo, giant ground sloth, running jesus lizard). This primitive mechanical gyroscope was replaced by genetic software improvements enabling reduced body bone weight (esp. femur & occiput), faster & longer
    bipedal locomotion, drastically reduced climbing/brachiating abilities.

    Casually walking while chewing gum, chatting and carrying a squirming child is something only humans could ever do.
    @378 cm^3, S. tchadensis' braincase is similar to that of extant
    chimpanzees and approximately a third the size of modern human brains.
    S chadensis was imo not a habitual nor obligate terrestrial orthograde biped, nor a part-time knucklewalking terrestrial quadruped, its foramen magnum reflected a more primitive arboreal orthograde bipedalism associated with
    suspensory slow brachiation x arboreal bipedalism, as in European miocene - pliocene apes and similar to but distinct from faster extant gibbons.

    Chimps & gorillas became more quadrupedal (partly pronograde terrestrial knucklewalking) while Homo became more bipedal (fully orthograde habitual obligate terrestrial striding), these produced changes of position and orientation of
    the foramen magnum.

    https://carta.anthropogeny.org/moca/topics/foramen-magnum-placement#:~:text=The%20foramen%20magnum%20position%20has,case%20for%20Ardipithecus%20and%20Sahelanthropus.
    The authors of the paper Erika cited disagree with your opinion.
    They might be right.
    If only there were some way to judge between contrasting opinions...

    Parsimony is good.
    Please direct me to the author(s) who disagree with what I wrote earlier. I don't know where to start, which vid, which paper... I'll examine inconsistencies (their or mine).
    Once again, watch the cited video. Erika identifies the paper in the
    first few minutes of the first vdeo. But if you watch/listen to all
    of both, you might actually learn something.
    Ok, I'd watched half of the 2nd video. I'll watch both tomorrow. I'll certainly learn something, I always do. For now, I stand behind every word I wrote earlier about Homo & Sahelanthropus.
    After a sneak peek, I see the paper, Postcranial ..., about the femur. I've skimmed it, no change in my thinking. But I'm flexible.
    I am so far sorely disappointed. At around 8:23, Erika intelligently but ignorantly describes the position of the foramen magnum and its significance. To her, bipedalism is terrestrial bipedalism. That is the central flaw in the study of
    hominoid, hominin & Homo evolution, one which I have already specifically addressed earlier. She and the various authors seem to be unable to comprehend the significance of arboreal habitual bipedalism. The authors do not disagree with my opinion, they
    are not even aware of the concept that bipedalism led to ape quadrupedalism. Erika is bright, but as blind as they are on this. More tomorrow, hopefully more enlightening.
    I acknowledge in the first video Erika mostly uses "bipedalism"
    without distinction between arboreal and terrestrial. However, her
    argument explicitly distinguishes between hominin and panin, and also >> >> > explicitly mentions terrestrial bipedality once. My understanding is >> >> > Erika uses hominin v panin to distinguish terrestrial v arboreal
    bipedalism. I could be wrong.

    Also, in the second video, Erika explicitly identifies arboreal
    bipedalism as an enabling adaptation to terrestrial bipedalism. So to >> >> > say she doesn't comprehend its significance is an exaggeration at
    least.

    Erika is careful for copyright purposes to limit how much of the cited >> >> > paper she includes in her video, so I can't say if the paper's authors >> >> > make an explicit distinction between arboreal and terrestrial
    bipedalism. Someone who has access to the full paper will have to
    weigh in on that point.

    However, Erika does mention that the paper discusses anatomical
    features of the femur (proto linear aspira, gluteal tuberosity, calcar >> >> > femoral {sp?}), and cortical bone of the ulnae. My understanding is
    these features are not present in arboreal bipedal species, and
    instead indicate the more robust musculature of terrestrial
    bipedalism.

    Finally, Erika's expressed reservation with the paper is if the
    evidence supports habitual bipedalism. She argues that would inform
    whether the common ancestor between hominin and panin was more
    human-like or more chimpanzee-like.
    My written response was lost. Damn. 15 sentences evaporated.
    Been there, done that. I agree it suks.
    The data graphs have nothing about hylobatids or macaques, so are worthless.
    Near the end of video one, Erika talks about 'bipedal or arboreal', revealing that she still doesn't get it.
    J: "these features are not present in arboreal bipedal species"
    I can't find where Erika says that,

    Possibly video 2.


    I can't find your quote in either video. Why don't you know where you
    got that quote?


    but I suspect she's referring to
    the 4 anatomical features of the tibia [femur] and ulnae I mention above. What
    arboreal bipedal species do you know with these features?

    All, in a spectrum, Homo at one end, arboreals the other.


    I am hard-pressed to describe extant humans as arboreal bipeds. Human
    are likely descended from arboreal bipeds, but it's a derived
    characteristic.


    Extant knucklewalking apes which sleep in bowl nests? Humans are gracile terrestrial bipeds.
    Not even mentioned: gibbons and humans share long achilles tendon and long lower back, opposite of extant great apes.
    Do the cited papers mention these things? If not, that would explain
    why Erika doesn't either.

    *Human bipedalism* cannot be *explained* without it. (It can be discussed & lectured, but not explained.) Picking out a few unique features and ignoring others doesn't explain anything.

    There's also this: https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-022-08828-7
    Not sure what chromosome 2 fusion has to do with this topic. Please
    elaborate.
    H/P split estimated timing .9ma is much later than MSC (Medit. & Red Sea dried out); H erectus bridged the est. date, so would have had 24, not 23 like Hs. I doubt their estimate.


    I acknowledge that chromosome 2 distinguishes extant humans from all
    other extant apes, and that the most parsimonious explanation is that
    the fusion event happened after the LCA of humans and other extant
    apes.

    According to this:
    <https://en.wikipedia.org/wiki/Hominini>

    LCA of gibbons and humans existed around 15.7 mya.
    LCA of orangs and humans existed around 8.8 mya.
    LCA of gorillas and humans existed around 6.3 mya.
    LCA of chimpanzees and humans existed some time after that, with no
    specified date. I have read other articles which suggest 4 mya.

    So your cited paper's estimated date for the fusion event of 0.9 mya
    is well after those dates. I agree that sounds very recent, but
    either way doesn't inform when the human lineage first began
    terrestrial bipedalism. As Erika points out, arboreal bipedalism can
    be precursor to both knuckle-walking and human terrestrial bipedalism.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Sun Oct 30 00:42:50 2022
    On Sunday, October 30, 2022 at 2:40:46 AM UTC-4, 69jp...@gmail.com wrote:
    On Sat, 29 Oct 2022 05:26:51 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Saturday, October 29, 2022 at 2:11:43 AM UTC-4, 69jp...@gmail.com wrote: >> On Fri, 28 Oct 2022 21:26:43 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, October 28, 2022 at 5:45:10 PM UTC-4, Daud Deden wrote:
    On Friday, October 28, 2022 at 4:45:58 AM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 21:53:46 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, October 28, 2022 at 12:20:59 AM UTC-4, Daud Deden wrote: >> >> > >> On Friday, October 28, 2022 at 12:13:33 AM UTC-4, Daud Deden wrote:
    On Thursday, October 27, 2022 at 10:56:53 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 16:44:19 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, October 27, 2022 at 5:53:29 AM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 02:17:42 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 7:56:43 PM UTC-4, 69jp...@gmail.com wrote:
    On Wed, 26 Oct 2022 03:17:08 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 4:10:49 AM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 16:32:06 -0700 (PDT), Daud Deden >> >> > >> > > >> >> >> <daud....@gmail.com> wrote:

    On Tuesday, October 25, 2022 at 6:59:05 PM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 01:18:27 -0700, Trolidan7
    <Trol...@eternal-september.org> wrote:

    On 10/23/22 11:50 PM, jillery wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Erika. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE> >> >> > >> > > >> >> >> >> >>
    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps> >> >> > >> > > >> >> >> >> >>
    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    I tend to think of it as none of the above.

    Simply because it is not that easy to stand upright.

    When an animal stands upright you need to solve a problem -
    how do you keep from falling over forward and backward.

    This might seem simple but it is not because with a four
    footed animal the center of gravity forward and backward
    is between the front legs and the back legs, and often
    that is a greater distance than between the left legs and
    the right legs.
    Watch the cited videos. Erika points out the challenges of going from
    quadruped to biped, the differences between upright posture and
    bipedalism, and the plausibility of suspensory orthograde posture in
    trees as a precursor to bipedalism on the ground. >> >> > >> > > >> >> >> >> >Some animals that sort of walk on twos have not solved the
    problem - a kangaroo can hop but in general it can not
    stably stand. Either way, in essence, the long hand enables
    force to be supplied to the far front and far back to counter
    falling forward or backward - the forefoot and big toe are
    the front force appliers and the heel is the back force
    applier. Then of course there are some animals that might
    sort of walk on threes (I am thinking of the Jerboa) - but
    humans have an extra problem because they have no tail to
    possibly act as an extra walking limb, or at least a balance.
    That's why humans like big butts, I can not lie. >> >> > >> > > >> >> >> >
    Bigger butt bones, bigger brain bones, initially. >> >> > >> > > >> >> >> >Homo erectus had unusually thick dense femurs and unusually thick dense occiputs (rear skull bone), which counterbalanced the pace over orthogonal bipedal treks on the ground, substituting for the more typical long dense tail
    of other bipeds (T rex, giant short faced kangaroo, giant ground sloth, running jesus lizard). This primitive mechanical gyroscope was replaced by genetic software improvements enabling reduced body bone weight (esp. femur & occiput), faster & longer
    bipedal locomotion, drastically reduced climbing/brachiating abilities.

    Casually walking while chewing gum, chatting and carrying a squirming child is something only humans could ever do.
    @378 cm^3, S. tchadensis' braincase is similar to that of extant
    chimpanzees and approximately a third the size of modern human brains.
    S chadensis was imo not a habitual nor obligate terrestrial orthograde biped, nor a part-time knucklewalking terrestrial quadruped, its foramen magnum reflected a more primitive arboreal orthograde bipedalism associated with
    suspensory slow brachiation x arboreal bipedalism, as in European miocene - pliocene apes and similar to but distinct from faster extant gibbons.

    Chimps & gorillas became more quadrupedal (partly pronograde terrestrial knucklewalking) while Homo became more bipedal (fully orthograde habitual obligate terrestrial striding), these produced changes of position and orientation
    of the foramen magnum.

    https://carta.anthropogeny.org/moca/topics/foramen-magnum-placement#:~:text=The%20foramen%20magnum%20position%20has,case%20for%20Ardipithecus%20and%20Sahelanthropus.
    The authors of the paper Erika cited disagree with your opinion.
    They might be right.
    If only there were some way to judge between contrasting opinions...

    Parsimony is good.
    Please direct me to the author(s) who disagree with what I wrote earlier. I don't know where to start, which vid, which paper... I'll examine inconsistencies (their or mine).
    Once again, watch the cited video. Erika identifies the paper in the
    first few minutes of the first vdeo. But if you watch/listen to all
    of both, you might actually learn something.
    Ok, I'd watched half of the 2nd video. I'll watch both tomorrow. I'll certainly learn something, I always do. For now, I stand behind every word I wrote earlier about Homo & Sahelanthropus.
    After a sneak peek, I see the paper, Postcranial ..., about the femur. I've skimmed it, no change in my thinking. But I'm flexible.
    I am so far sorely disappointed. At around 8:23, Erika intelligently but ignorantly describes the position of the foramen magnum and its significance. To her, bipedalism is terrestrial bipedalism. That is the central flaw in the study of
    hominoid, hominin & Homo evolution, one which I have already specifically addressed earlier. She and the various authors seem to be unable to comprehend the significance of arboreal habitual bipedalism. The authors do not disagree with my opinion, they
    are not even aware of the concept that bipedalism led to ape quadrupedalism. Erika is bright, but as blind as they are on this. More tomorrow, hopefully more enlightening.
    I acknowledge in the first video Erika mostly uses "bipedalism"
    without distinction between arboreal and terrestrial. However, her >> >> > argument explicitly distinguishes between hominin and panin, and also
    explicitly mentions terrestrial bipedality once. My understanding is >> >> > Erika uses hominin v panin to distinguish terrestrial v arboreal
    bipedalism. I could be wrong.

    Also, in the second video, Erika explicitly identifies arboreal
    bipedalism as an enabling adaptation to terrestrial bipedalism. So to
    say she doesn't comprehend its significance is an exaggeration at
    least.

    Erika is careful for copyright purposes to limit how much of the cited
    paper she includes in her video, so I can't say if the paper's authors
    make an explicit distinction between arboreal and terrestrial
    bipedalism. Someone who has access to the full paper will have to
    weigh in on that point.

    However, Erika does mention that the paper discusses anatomical
    features of the femur (proto linear aspira, gluteal tuberosity, calcar
    femoral {sp?}), and cortical bone of the ulnae. My understanding is >> >> > these features are not present in arboreal bipedal species, and
    instead indicate the more robust musculature of terrestrial
    bipedalism.

    Finally, Erika's expressed reservation with the paper is if the
    evidence supports habitual bipedalism. She argues that would inform >> >> > whether the common ancestor between hominin and panin was more
    human-like or more chimpanzee-like.
    My written response was lost. Damn. 15 sentences evaporated.
    Been there, done that. I agree it suks.
    The data graphs have nothing about hylobatids or macaques, so are worthless.
    Near the end of video one, Erika talks about 'bipedal or arboreal', revealing that she still doesn't get it.
    J: "these features are not present in arboreal bipedal species"
    I can't find where Erika says that,

    Possibly video 2.
    I can't find your quote in either video. Why don't you know where you
    got that quote?

    The quote by Erica was "bipedal or arboreal" (or VV). It was referenced amongst the 15 vaporised sentences. I can't watch the videos again until I get to a computer, youtube burns cell phone data too quick. Monday.

    but I suspect she's referring to
    the 4 anatomical features of the tibia [femur] and ulnae I mention above. What
    arboreal bipedal species do you know with these features?

    All, in a spectrum, Homo at one end, arboreals the other.
    I am hard-pressed to describe extant humans as arboreal bipeds.

    Probable part-time arboreal bipeds: Homo habilis, georgicus, naledi, florensis, etc.

    Human
    are likely descended from arboreal bipeds, but it's a derived characteristic.
    Extant knucklewalking apes which sleep in bowl nests? Humans are gracile terrestrial bipeds.
    Not even mentioned: gibbons and humans share long achilles tendon and long lower back, opposite of extant great apes.
    Do the cited papers mention these things? If not, that would explain
    why Erika doesn't either.

    *Human bipedalism* cannot be *explained* without it. (It can be discussed & lectured, but not explained.) Picking out a few unique features and ignoring others doesn't explain anything.

    There's also this: https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-022-08828-7
    Not sure what chromosome 2 fusion has to do with this topic. Please
    elaborate.
    H/P split estimated timing .9ma is much later than MSC (Medit. & Red Sea dried out); H erectus bridged the est. date, so would have had 24, not 23 like Hs. I doubt their estimate.
    I acknowledge that chromosome 2 distinguishes extant humans from all
    other extant apes, and that the most parsimonious explanation is that
    the fusion event happened after the LCA of humans and other extant
    apes.

    Rather, during, imo.

    According to this:
    <https://en.wikipedia.org/wiki/Hominini>

    LCA of gibbons and humans existed around 15.7 mya.
    LCA of orangs and humans existed around 8.8 mya.
    LCA of gorillas and humans existed around 6.3 mya.
    LCA of chimpanzees and humans existed some time after that, with no specified date. I have read other articles which suggest 4 mya.

    So your cited paper's estimated date for the fusion event of 0.9 mya
    is well after those dates. I agree that sounds very recent, but
    either way doesn't inform when the human lineage first began
    terrestrial bipedalism.

    True.

    As Erika points out, arboreal bipedalism can
    be precursor to both knuckle-walking and human terrestrial bipedalism.

    Yes, of course. Can & was, alongside arboreal bimanualism (slow brachiation).

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to daud.deden@gmail.com on Sun Oct 30 10:46:42 2022
    On Sun, 30 Oct 2022 00:42:50 -0700 (PDT), Daud Deden
    <daud.deden@gmail.com> wrote:

    On Sunday, October 30, 2022 at 2:40:46 AM UTC-4, 69jp...@gmail.com wrote:
    On Sat, 29 Oct 2022 05:26:51 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Saturday, October 29, 2022 at 2:11:43 AM UTC-4, 69jp...@gmail.com wrote:
    On Fri, 28 Oct 2022 21:26:43 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, October 28, 2022 at 5:45:10 PM UTC-4, Daud Deden wrote:
    On Friday, October 28, 2022 at 4:45:58 AM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 21:53:46 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, October 28, 2022 at 12:20:59 AM UTC-4, Daud Deden wrote:
    On Friday, October 28, 2022 at 12:13:33 AM UTC-4, Daud Deden wrote:
    On Thursday, October 27, 2022 at 10:56:53 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 16:44:19 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, October 27, 2022 at 5:53:29 AM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 02:17:42 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 7:56:43 PM UTC-4, 69jp...@gmail.com wrote:
    On Wed, 26 Oct 2022 03:17:08 -0700 (PDT), Daud Deden >> >> >> > >> > > >> >> <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 4:10:49 AM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 16:32:06 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, October 25, 2022 at 6:59:05 PM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 01:18:27 -0700, Trolidan7
    <Trol...@eternal-september.org> wrote:

    On 10/23/22 11:50 PM, jillery wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Erika. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE> >> >> >> > >> > > >> >> >> >> >>
    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps> >> >> >> > >> > > >> >> >> >> >>
    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    I tend to think of it as none of the above.

    Simply because it is not that easy to stand upright.

    When an animal stands upright you need to solve a problem -
    how do you keep from falling over forward and backward.

    This might seem simple but it is not because with a four
    footed animal the center of gravity forward and backward
    is between the front legs and the back legs, and often
    that is a greater distance than between the left legs and
    the right legs.
    Watch the cited videos. Erika points out the challenges of going from
    quadruped to biped, the differences between upright posture and
    bipedalism, and the plausibility of suspensory orthograde posture in
    trees as a precursor to bipedalism on the ground.
    Some animals that sort of walk on twos have not solved the
    problem - a kangaroo can hop but in general it can not
    stably stand. Either way, in essence, the long hand enables
    force to be supplied to the far front and far back to counter
    falling forward or backward - the forefoot and big toe are
    the front force appliers and the heel is the back force
    applier. Then of course there are some animals that might
    sort of walk on threes (I am thinking of the Jerboa) - but
    humans have an extra problem because they have no tail to
    possibly act as an extra walking limb, or at least a balance.
    That's why humans like big butts, I can not lie. >> >> >> > >> > > >> >> >> >
    Bigger butt bones, bigger brain bones, initially. >> >> >> > >> > > >> >> >> >Homo erectus had unusually thick dense femurs and unusually thick dense occiputs (rear skull bone), which counterbalanced the pace over orthogonal bipedal treks on the ground, substituting for the more typical long dense tail
    of other bipeds (T rex, giant short faced kangaroo, giant ground sloth, running jesus lizard). This primitive mechanical gyroscope was replaced by genetic software improvements enabling reduced body bone weight (esp. femur & occiput), faster & longer
    bipedal locomotion, drastically reduced climbing/brachiating abilities.

    Casually walking while chewing gum, chatting and carrying a squirming child is something only humans could ever do.
    @378 cm^3, S. tchadensis' braincase is similar to that of extant
    chimpanzees and approximately a third the size of modern human brains.
    S chadensis was imo not a habitual nor obligate terrestrial orthograde biped, nor a part-time knucklewalking terrestrial quadruped, its foramen magnum reflected a more primitive arboreal orthograde bipedalism associated with
    suspensory slow brachiation x arboreal bipedalism, as in European miocene - pliocene apes and similar to but distinct from faster extant gibbons.

    Chimps & gorillas became more quadrupedal (partly pronograde terrestrial knucklewalking) while Homo became more bipedal (fully orthograde habitual obligate terrestrial striding), these produced changes of position and orientation
    of the foramen magnum.

    https://carta.anthropogeny.org/moca/topics/foramen-magnum-placement#:~:text=The%20foramen%20magnum%20position%20has,case%20for%20Ardipithecus%20and%20Sahelanthropus.
    The authors of the paper Erika cited disagree with your opinion.
    They might be right.
    If only there were some way to judge between contrasting opinions...

    Parsimony is good.
    Please direct me to the author(s) who disagree with what I wrote earlier. I don't know where to start, which vid, which paper... I'll examine inconsistencies (their or mine).
    Once again, watch the cited video. Erika identifies the paper in the
    first few minutes of the first vdeo. But if you watch/listen to all
    of both, you might actually learn something.
    Ok, I'd watched half of the 2nd video. I'll watch both tomorrow. I'll certainly learn something, I always do. For now, I stand behind every word I wrote earlier about Homo & Sahelanthropus.
    After a sneak peek, I see the paper, Postcranial ..., about the femur. I've skimmed it, no change in my thinking. But I'm flexible.
    I am so far sorely disappointed. At around 8:23, Erika intelligently but ignorantly describes the position of the foramen magnum and its significance. To her, bipedalism is terrestrial bipedalism. That is the central flaw in the study of
    hominoid, hominin & Homo evolution, one which I have already specifically addressed earlier. She and the various authors seem to be unable to comprehend the significance of arboreal habitual bipedalism. The authors do not disagree with my opinion, they
    are not even aware of the concept that bipedalism led to ape quadrupedalism. Erika is bright, but as blind as they are on this. More tomorrow, hopefully more enlightening.
    I acknowledge in the first video Erika mostly uses "bipedalism"
    without distinction between arboreal and terrestrial. However, her >> >> >> > argument explicitly distinguishes between hominin and panin, and also
    explicitly mentions terrestrial bipedality once. My understanding is
    Erika uses hominin v panin to distinguish terrestrial v arboreal
    bipedalism. I could be wrong.

    Also, in the second video, Erika explicitly identifies arboreal
    bipedalism as an enabling adaptation to terrestrial bipedalism. So to
    say she doesn't comprehend its significance is an exaggeration at >> >> >> > least.

    Erika is careful for copyright purposes to limit how much of the cited
    paper she includes in her video, so I can't say if the paper's authors
    make an explicit distinction between arboreal and terrestrial
    bipedalism. Someone who has access to the full paper will have to >> >> >> > weigh in on that point.

    However, Erika does mention that the paper discusses anatomical
    features of the femur (proto linear aspira, gluteal tuberosity, calcar
    femoral {sp?}), and cortical bone of the ulnae. My understanding is >> >> >> > these features are not present in arboreal bipedal species, and
    instead indicate the more robust musculature of terrestrial
    bipedalism.

    Finally, Erika's expressed reservation with the paper is if the
    evidence supports habitual bipedalism. She argues that would inform >> >> >> > whether the common ancestor between hominin and panin was more
    human-like or more chimpanzee-like.
    My written response was lost. Damn. 15 sentences evaporated.
    Been there, done that. I agree it suks.
    The data graphs have nothing about hylobatids or macaques, so are worthless.
    Near the end of video one, Erika talks about 'bipedal or arboreal', revealing that she still doesn't get it.
    J: "these features are not present in arboreal bipedal species"
    I can't find where Erika says that,

    Possibly video 2.
    I can't find your quote in either video. Why don't you know where you
    got that quote?

    The quote by Erica was "bipedal or arboreal" (or VV). It was referenced amongst the 15 vaporised sentences. I can't watch the videos again until I get to a computer, youtube burns cell phone data too quick. Monday.


    I agree that videos on cell phones can be a challenge. As a rule, I
    try to piggyback on open WiFi while using a VPN.

    Alternately, ignore the video and read the transcript. On my Android,
    below the video is the video title. To the right is a down caret. Tap
    on the caret brings up the video description which has a "show
    transcript" window. Tap on the window brings up the transcript, which
    is text searchable without burning too much data.

    I acknowledge it's all much easier on a full screen. FWIW I didn't
    find either quote in either video.


    but I suspect she's referring to
    the 4 anatomical features of the tibia [femur] and ulnae I mention above. What
    arboreal bipedal species do you know with these features?

    All, in a spectrum, Homo at one end, arboreals the other.
    I am hard-pressed to describe extant humans as arboreal bipeds.

    Probable part-time arboreal bipeds: Homo habilis, georgicus, naledi, florensis, etc.


    So you don't mean H.sapiens or H. neanderthalensis.


    Human
    are likely descended from arboreal bipeds, but it's a derived
    characteristic.
    Extant knucklewalking apes which sleep in bowl nests? Humans are gracile terrestrial bipeds.
    Not even mentioned: gibbons and humans share long achilles tendon and long lower back, opposite of extant great apes.
    Do the cited papers mention these things? If not, that would explain
    why Erika doesn't either.

    *Human bipedalism* cannot be *explained* without it. (It can be discussed & lectured, but not explained.) Picking out a few unique features and ignoring others doesn't explain anything.

    There's also this: https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-022-08828-7
    Not sure what chromosome 2 fusion has to do with this topic. Please
    elaborate.
    H/P split estimated timing .9ma is much later than MSC (Medit. & Red Sea dried out); H erectus bridged the est. date, so would have had 24, not 23 like Hs. I doubt their estimate.
    I acknowledge that chromosome 2 distinguishes extant humans from all
    other extant apes, and that the most parsimonious explanation is that
    the fusion event happened after the LCA of humans and other extant
    apes.

    Rather, during, imo.


    Of course it's possible the fusion event coincidentally happened
    during LCA, but less likely and not necessary. The chromosome 2
    fusion wouldn't have caused any loss of genetic information or a
    speciation event, at least not initially. So it's more likely to have
    happened somewhere between 4 mya and 0.9 mya.


    According to this:
    <https://en.wikipedia.org/wiki/Hominini>

    LCA of gibbons and humans existed around 15.7 mya.
    LCA of orangs and humans existed around 8.8 mya.
    LCA of gorillas and humans existed around 6.3 mya.
    LCA of chimpanzees and humans existed some time after that, with no
    specified date. I have read other articles which suggest 4 mya.

    So your cited paper's estimated date for the fusion event of 0.9 mya
    is well after those dates. I agree that sounds very recent, but
    either way doesn't inform when the human lineage first began
    terrestrial bipedalism.

    True.

    As Erika points out, arboreal bipedalism can
    be precursor to both knuckle-walking and human terrestrial bipedalism.

    Yes, of course. Can & was, alongside arboreal bimanualism (slow brachiation).

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Trolidan7@21:1/5 to Peter Nyikos on Sun Oct 30 09:11:39 2022
    On 10/27/22 7:26 PM, Peter Nyikos wrote:
    On Tuesday, October 25, 2022 at 4:18:31 AM UTC-4, Trolidan7 wrote:
    On 10/23/22 11:50 PM, jillery wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    I tend to think of it as none of the above.

    Did you watch the video, to see what they were?

    I did watch nearly all of both.

    In general she studied questions about the nature
    of the environmental factors that may have produced
    bipedalism rather than the factors involving the
    specific dynamics of walking.

    I once partially remember a teacher a long time
    ago saying science does not ask 'why' questions.

    I argued that one could rephrase questions so
    that they were essentially the same either using
    or not using the word 'why'. Reasonably, if
    the question is short enough it can have an array
    of meanings and what is referred to can be unclear.

    This was about 30 years ago and it would take a while
    to remember which specific class or subject.

    About 'blood and lymph' and the nature of where
    copper is on a cellular and extracellular level
    in invertebrates and giving a reference I am also
    sorry. It could take an incredible amount of digging
    to find where and when I read that and I could still
    be off when it comes to precisely when or where I
    might have done that. I could be way off.

    For the video I did that a few days ago.

    Granted, with an open-ended subject like bipedalism, it is quite
    unlikely that any "why" that we humans can easily formulate
    gives a reason that is anywhere near complete. It's almost
    as bad as theories about how we developed such amazingly
    sophisticated speech. Simplified theories have been
    given derisive names like "bow-wow theory" and "ding-dong theory"
    or even been accused of being "pseudoscientific."

    Simply because it is not that easy to stand upright.

    When an animal stands upright you need to solve a problem -
    how do you keep from falling over forward and backward.

    This might seem simple but it is not because with a four
    footed animal the center of gravity forward and backward
    is between the front legs and the back legs, and often
    that is a greater distance than between the left legs and
    the right legs.

    Some animals that sort of walk on twos have not solved the
    problem - a kangaroo can hop but in general it can not
    stably stand.

    On the other hand, sifakas, the avahi, and the indri -- all lemurs -- are even more
    obligate bipedal than we are: their forelimbs are even shorter
    in proportion to their hindlimbs than ours are.

    Their primary way of getting from one place to another
    is fully bipedal hopping, generally between trees.
    However, I have a book with a photograph
    in which a sifaka has a very typically human style
    running pose, with arms swinging in opposite
    orientation to her wide-apart (from front to back) legs.

    She gave the idea that the apes may have once been
    more bipedal, and then specialized for four legged
    walking in chimps and gorillas and specialized for
    bipedal walking in humans, and she did not specify
    precisely what she was referring to. What you
    are typing, however, may have parallels in natural
    history that are what she is referring to.

    Often the word 'walking' tends to imply locomotion
    on the ground, but when you are climbing up, down,
    or across a tree it can in some ways be motion
    across a different substrate, just as 'swimming',
    'walking', are 'flying' can often be thought of
    as different things, involving substrates of liquid,
    a solid ground, or air.

    Are we obligate bipeds? For humans, it is possible
    to crawl but that is rare. That tends to be most
    commonly used. Do many apes or monkeys have four
    'hands'? Often we tend to use the word 'hand' for
    a limb that tends to manipulate objects, and 'wing'
    for one that tends to fly. But if an animal is
    moving by transferring to different locations on
    or between trees, then the boundary between 'moving'
    and 'manipulating objects' may be blurred.

    It was several days ago, and I would have to rewatch
    it again to summarize the different theories that
    she gave and the specific one that she supported.

    Admittedly, it was generally a different question.

    Either way, in essence, the long hand enables
    force to be supplied >> to the far front and far back to counter
    falling forward or backward - the forefoot and big toe are
    the front force appliers and the heel is the back force
    applier. Then of course there are some animals that might
    sort of walk on threes (I am thinking of the Jerboa) - but
    humans have an extra problem because they have no tail to
    possibly act as an extra walking limb, or at least a balance.

    Indris have almost lost their tails, but you've made me wonder
    whether the long, narrow tail of that sifaka was an aid in
    balancing, making that human-like stride possible.


    Peter Nyikos
    Professor, Dept. of Mathematics -- standard disclaimer--
    Univ. of South Carolina at Columbia
    http://people.math.sc.edu/nyikos


    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Trolidan7@21:1/5 to Peter Nyikos on Sun Oct 30 09:23:01 2022
    On 10/27/22 6:42 PM, Peter Nyikos wrote:
    How about that! You, who seldom post here, actually did an on-topic OP.
    This puts you ahead of John Harshman: in the almost dozen years
    since I returned here, I don't recall him ever doing an on-topic OP to sci.bio.paleontology.
    This despite the fact that he has probably done a few thousand posts
    here in that time.

    I do have a few recommendations. The optimal place to post information about homini is sci.anthropology.paleo. Not only are they the "specialty" of that ng,
    it is more active, with more regulars than s.b.p. Best of all perhaps, Pandora
    takes a very active part there, going into depth with one person after another.
    Pandora occasionally posts to s.b.p. too, but the majority of her posts here are OP's.
    They are almost invariably excellent and thought-provoking, but she seldom comments on the thoughts she has provoked, even when they are on-topic
    in every sense of the word.

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:

    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis.

    I don't have enough time this evening to watch either this video or
    the one you mention below. This being a science ng, it is very
    appropriate to give the titles of these papers. Those of us who
    are interested in research papers shouldn't have to sit through a video
    to find out what they are.


    This fossil is remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    In science, hypotheses on such an open ended theme are seldom
    compelling. Before you decide to post this to s.a.p., I strongly recommend that you state this preferred hypothesis; some people there may already
    have heard of it (especially Pandora, who comes across as a professional
    well past the age of earning the Ph.D.) and have formulated ideas about it.

    Then there is of course the question, 'what is science',
    is it knowledge in general, a specific subset of all
    knowledge, or a specific subset of ways of acquiring
    knowledge? Then again, maybe this type of question
    is a 'philosophy' question. But of you are just enough
    unclear in just the right way, you can ask 'what is
    philosophy' and make the question not obviously fall
    in either category.

    Peter Nyikos
    Professor, Dept. of Mathematics -- standard disclaimer--
    University of South Carolina
    http://people.math.sc.edu/nyikos


    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Sun Oct 30 09:52:58 2022
    On Sunday, October 30, 2022 at 10:46:43 AM UTC-4, 69jp...@gmail.com wrote:
    On Sun, 30 Oct 2022 00:42:50 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Sunday, October 30, 2022 at 2:40:46 AM UTC-4, 69jp...@gmail.com wrote: >> On Sat, 29 Oct 2022 05:26:51 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Saturday, October 29, 2022 at 2:11:43 AM UTC-4, 69jp...@gmail.com wrote:
    On Fri, 28 Oct 2022 21:26:43 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, October 28, 2022 at 5:45:10 PM UTC-4, Daud Deden wrote:
    On Friday, October 28, 2022 at 4:45:58 AM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 21:53:46 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, October 28, 2022 at 12:20:59 AM UTC-4, Daud Deden wrote:
    On Friday, October 28, 2022 at 12:13:33 AM UTC-4, Daud Deden wrote:
    On Thursday, October 27, 2022 at 10:56:53 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 16:44:19 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, October 27, 2022 at 5:53:29 AM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 27 Oct 2022 02:17:42 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 7:56:43 PM UTC-4, 69jp...@gmail.com wrote:
    On Wed, 26 Oct 2022 03:17:08 -0700 (PDT), Daud Deden >> >> >> > >> > > >> >> <daud....@gmail.com> wrote:

    On Wednesday, October 26, 2022 at 4:10:49 AM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 16:32:06 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, October 25, 2022 at 6:59:05 PM UTC-4, 69jp...@gmail.com wrote:
    On Tue, 25 Oct 2022 01:18:27 -0700, Trolidan7 >> >> >> > >> > > >> >> >> >> <Trol...@eternal-september.org> wrote:

    On 10/23/22 11:50 PM, jillery wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Erika. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    I tend to think of it as none of the above. >> >> >> > >> > > >> >> >> >> >
    Simply because it is not that easy to stand upright.

    When an animal stands upright you need to solve a problem -
    how do you keep from falling over forward and backward.

    This might seem simple but it is not because with a four
    footed animal the center of gravity forward and backward
    is between the front legs and the back legs, and often
    that is a greater distance than between the left legs and
    the right legs.
    Watch the cited videos. Erika points out the challenges of going from
    quadruped to biped, the differences between upright posture and
    bipedalism, and the plausibility of suspensory orthograde posture in
    trees as a precursor to bipedalism on the ground.
    Some animals that sort of walk on twos have not solved the
    problem - a kangaroo can hop but in general it can not
    stably stand. Either way, in essence, the long hand enables
    force to be supplied to the far front and far back to counter
    falling forward or backward - the forefoot and big toe are
    the front force appliers and the heel is the back force
    applier. Then of course there are some animals that might
    sort of walk on threes (I am thinking of the Jerboa) - but
    humans have an extra problem because they have no tail to
    possibly act as an extra walking limb, or at least a balance.
    That's why humans like big butts, I can not lie.

    Bigger butt bones, bigger brain bones, initially.
    Homo erectus had unusually thick dense femurs and unusually thick dense occiputs (rear skull bone), which counterbalanced the pace over orthogonal bipedal treks on the ground, substituting for the more typical long dense
    tail of other bipeds (T rex, giant short faced kangaroo, giant ground sloth, running jesus lizard). This primitive mechanical gyroscope was replaced by genetic software improvements enabling reduced body bone weight (esp. femur & occiput), faster &
    longer bipedal locomotion, drastically reduced climbing/brachiating abilities.

    Casually walking while chewing gum, chatting and carrying a squirming child is something only humans could ever do.
    @378 cm^3, S. tchadensis' braincase is similar to that of extant
    chimpanzees and approximately a third the size of modern human brains.
    S chadensis was imo not a habitual nor obligate terrestrial orthograde biped, nor a part-time knucklewalking terrestrial quadruped, its foramen magnum reflected a more primitive arboreal orthograde bipedalism associated with
    suspensory slow brachiation x arboreal bipedalism, as in European miocene - pliocene apes and similar to but distinct from faster extant gibbons.

    Chimps & gorillas became more quadrupedal (partly pronograde terrestrial knucklewalking) while Homo became more bipedal (fully orthograde habitual obligate terrestrial striding), these produced changes of position and
    orientation of the foramen magnum.

    https://carta.anthropogeny.org/moca/topics/foramen-magnum-placement#:~:text=The%20foramen%20magnum%20position%20has,case%20for%20Ardipithecus%20and%20Sahelanthropus.
    The authors of the paper Erika cited disagree with your opinion.
    They might be right.
    If only there were some way to judge between contrasting opinions...

    Parsimony is good.
    Please direct me to the author(s) who disagree with what I wrote earlier. I don't know where to start, which vid, which paper... I'll examine inconsistencies (their or mine).
    Once again, watch the cited video. Erika identifies the paper in the
    first few minutes of the first vdeo. But if you watch/listen to all
    of both, you might actually learn something.
    Ok, I'd watched half of the 2nd video. I'll watch both tomorrow. I'll certainly learn something, I always do. For now, I stand behind every word I wrote earlier about Homo & Sahelanthropus.
    After a sneak peek, I see the paper, Postcranial ..., about the femur. I've skimmed it, no change in my thinking. But I'm flexible.
    I am so far sorely disappointed. At around 8:23, Erika intelligently but ignorantly describes the position of the foramen magnum and its significance. To her, bipedalism is terrestrial bipedalism. That is the central flaw in the study of
    hominoid, hominin & Homo evolution, one which I have already specifically addressed earlier. She and the various authors seem to be unable to comprehend the significance of arboreal habitual bipedalism. The authors do not disagree with my opinion, they
    are not even aware of the concept that bipedalism led to ape quadrupedalism. Erika is bright, but as blind as they are on this. More tomorrow, hopefully more enlightening.
    I acknowledge in the first video Erika mostly uses "bipedalism" >> >> >> > without distinction between arboreal and terrestrial. However, her
    argument explicitly distinguishes between hominin and panin, and also
    explicitly mentions terrestrial bipedality once. My understanding is
    Erika uses hominin v panin to distinguish terrestrial v arboreal >> >> >> > bipedalism. I could be wrong.

    Also, in the second video, Erika explicitly identifies arboreal >> >> >> > bipedalism as an enabling adaptation to terrestrial bipedalism. So to
    say she doesn't comprehend its significance is an exaggeration at >> >> >> > least.

    Erika is careful for copyright purposes to limit how much of the cited
    paper she includes in her video, so I can't say if the paper's authors
    make an explicit distinction between arboreal and terrestrial
    bipedalism. Someone who has access to the full paper will have to >> >> >> > weigh in on that point.

    However, Erika does mention that the paper discusses anatomical >> >> >> > features of the femur (proto linear aspira, gluteal tuberosity, calcar
    femoral {sp?}), and cortical bone of the ulnae. My understanding is
    these features are not present in arboreal bipedal species, and >> >> >> > instead indicate the more robust musculature of terrestrial
    bipedalism.

    Finally, Erika's expressed reservation with the paper is if the >> >> >> > evidence supports habitual bipedalism. She argues that would inform
    whether the common ancestor between hominin and panin was more
    human-like or more chimpanzee-like.
    My written response was lost. Damn. 15 sentences evaporated.
    Been there, done that. I agree it suks.
    The data graphs have nothing about hylobatids or macaques, so are worthless.
    Near the end of video one, Erika talks about 'bipedal or arboreal', revealing that she still doesn't get it.
    J: "these features are not present in arboreal bipedal species"
    I can't find where Erika says that,

    Possibly video 2.
    I can't find your quote in either video. Why don't you know where you
    got that quote?

    The quote by Erica was "bipedal or arboreal" (or VV). It was referenced amongst the 15 vaporised sentences. I can't watch the videos again until I get to a computer, youtube burns cell phone data too quick. Monday.
    I agree that videos on cell phones can be a challenge. As a rule, I
    try to piggyback on open WiFi while using a VPN.
    I'm often offgrid. Wifi when I can.

    Alternately, ignore the video and read the transcript. On my Android,
    below the video is the video title. To the right is a down caret. Tap
    on the caret brings up the video description which has a "show
    transcript" window. Tap on the window brings up the transcript, which
    is text searchable without burning too much data.
    Thanks, I didn't know about the transcript.

    I acknowledge it's all much easier on a full screen. FWIW I didn't
    find either quote in either video.
    Will dig.

    but I suspect she's referring to
    the 4 anatomical features of the tibia [femur] and ulnae I mention above. What
    arboreal bipedal species do you know with these features?

    All, in a spectrum, Homo at one end, arboreals the other.
    I am hard-pressed to describe extant humans as arboreal bipeds.

    Probable part-time arboreal bipeds: Homo habilis, georgicus, naledi, florensis, etc.
    So you don't mean H.sapiens or H. neanderthalensis.
    They are at the far end. Rainforest H&G do climb trees seeking seasonal foods, fruits, honey, nuts, and during war hide in tree nests, but otherwise are terrestrial. Neanderthals may have hunted from treestands. No Homo had a divergent hallux.
    I've seen many young men climb coconut palms in SEAsia w/o tools, just takes practice & thirst.

    Human
    are likely descended from arboreal bipeds, but it's a derived
    characteristic.
    Extant knucklewalking apes which sleep in bowl nests? Humans are gracile terrestrial bipeds.
    Not even mentioned: gibbons and humans share long achilles tendon and long lower back, opposite of extant great apes.
    Do the cited papers mention these things? If not, that would explain >> >> why Erika doesn't either.

    *Human bipedalism* cannot be *explained* without it. (It can be discussed & lectured, but not explained.) Picking out a few unique features and ignoring others doesn't explain anything.

    There's also this: https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-022-08828-7
    Not sure what chromosome 2 fusion has to do with this topic. Please
    elaborate.
    H/P split estimated timing .9ma is much later than MSC (Medit. & Red Sea dried out); H erectus bridged the est. date, so would have had 24, not 23 like Hs. I doubt their estimate.
    I acknowledge that chromosome 2 distinguishes extant humans from all
    other extant apes, and that the most parsimonious explanation is that
    the fusion event happened after the LCA of humans and other extant
    apes.

    Rather, during, imo.
    Of course it's possible the fusion event coincidentally happened
    during LCA, but less likely and not necessary.
    Uncertain, but I think there was causation. The chr 2 fusion also partly inverted the script, a rare thing; which I think produced speciation. No Homo is known to have 24/48 chromosomes.

    The chromosome 2
    fusion wouldn't have caused any loss of genetic information or a
    speciation event, at least not initially. So it's more likely to have happened somewhere between 4 mya and 0.9 mya.
    I'll stick with my conjecture.

    According to this:
    <https://en.wikipedia.org/wiki/Hominini>

    LCA of gibbons and humans existed around 15.7 mya.
    LCA of orangs and humans existed around 8.8 mya.
    LCA of gorillas and humans existed around 6.3 mya.
    LCA of chimpanzees and humans existed some time after that, with no
    specified date. I have read other articles which suggest 4 mya.

    So your cited paper's estimated date for the fusion event of 0.9 mya
    is well after those dates. I agree that sounds very recent, but
    either way doesn't inform when the human lineage first began
    terrestrial bipedalism.

    True.

    As Erika points out, arboreal bipedalism can
    be precursor to both knuckle-walking and human terrestrial bipedalism.

    Yes, of course. Can & was, alongside arboreal bimanualism (slow brachiation).

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to daud.deden@gmail.com on Sun Oct 30 17:17:45 2022
    On Sun, 30 Oct 2022 09:52:58 -0700 (PDT), Daud Deden
    <daud.deden@gmail.com> wrote:

    On Sunday, October 30, 2022 at 10:46:43 AM UTC-4, 69jp...@gmail.com wrote:

    <snip uncommented text for brevity>

    but I suspect she's referring to
    the 4 anatomical features of the tibia [femur] and ulnae I mention above. What
    arboreal bipedal species do you know with these features?

    All, in a spectrum, Homo at one end, arboreals the other.
    I am hard-pressed to describe extant humans as arboreal bipeds.

    Probable part-time arboreal bipeds: Homo habilis, georgicus, naledi, florensis, etc.
    So you don't mean H.sapiens or H. neanderthalensis.
    They are at the far end. Rainforest H&G do climb trees seeking seasonal foods, fruits, honey, nuts, and during war hide in tree nests, but otherwise are terrestrial. Neanderthals may have hunted from treestands. No Homo had a divergent hallux.
    I've seen many young men climb coconut palms in SEAsia w/o tools, just takes practice & thirst.


    I am hard-pressed to describe tree-climbing as arboreal bipedalism,
    especially the way those young men climb coconut palms.


    Human
    are likely descended from arboreal bipeds, but it's a derived
    characteristic.
    Extant knucklewalking apes which sleep in bowl nests? Humans are gracile terrestrial bipeds.
    Not even mentioned: gibbons and humans share long achilles tendon and long lower back, opposite of extant great apes.
    Do the cited papers mention these things? If not, that would explain >> >> >> why Erika doesn't either.

    *Human bipedalism* cannot be *explained* without it. (It can be discussed & lectured, but not explained.) Picking out a few unique features and ignoring others doesn't explain anything.

    There's also this: https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-022-08828-7
    Not sure what chromosome 2 fusion has to do with this topic. Please >> >> >> elaborate.
    H/P split estimated timing .9ma is much later than MSC (Medit. & Red Sea dried out); H erectus bridged the est. date, so would have had 24, not 23 like Hs. I doubt their estimate.
    I acknowledge that chromosome 2 distinguishes extant humans from all
    other extant apes, and that the most parsimonious explanation is that
    the fusion event happened after the LCA of humans and other extant
    apes.

    Rather, during, imo.
    Of course it's possible the fusion event coincidentally happened
    during LCA, but less likely and not necessary.
    Uncertain, but I think there was causation. The chr 2 fusion also partly inverted the script, a rare thing; which I think produced speciation. No Homo is known to have 24/48 chromosomes.


    I acknowledge the fusion event inverted part of chromosome 2. However,
    that didn't alter how genes are transcribed. This is a common
    misconception. For any given DNA sequence, there is a 5-prime end and
    a 3-prime end. Transcription from DNA to mRNA always starts from the
    5-prime end and ends at the 3-prime end:

    <https://www.thoughtco.com/steps-of-transcription-from-dna-to-rna-603895>


    The chromosome 2
    fusion wouldn't have caused any loss of genetic information or a
    speciation event, at least not initially. So it's more likely to have
    happened somewhere between 4 mya and 0.9 mya.
    I'll stick with my conjecture.


    Some molecular biology might help unstick you from your conjecture.


    According to this:
    <https://en.wikipedia.org/wiki/Hominini>

    LCA of gibbons and humans existed around 15.7 mya.
    LCA of orangs and humans existed around 8.8 mya.
    LCA of gorillas and humans existed around 6.3 mya.
    LCA of chimpanzees and humans existed some time after that, with no
    specified date. I have read other articles which suggest 4 mya.

    So your cited paper's estimated date for the fusion event of 0.9 mya
    is well after those dates. I agree that sounds very recent, but
    either way doesn't inform when the human lineage first began
    terrestrial bipedalism.

    True.

    As Erika points out, arboreal bipedalism can
    be precursor to both knuckle-walking and human terrestrial bipedalism. >> >
    Yes, of course. Can & was, alongside arboreal bimanualism (slow brachiation).

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Sun Oct 30 16:58:57 2022
    On Sunday, October 30, 2022 at 5:17:46 PM UTC-4, 69jp...@gmail.com wrote:
    On Sun, 30 Oct 2022 09:52:58 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Sunday, October 30, 2022 at 10:46:43 AM UTC-4, 69jp...@gmail.com wrote: <snip uncommented text for brevity>
    but I suspect she's referring to
    the 4 anatomical features of the tibia [femur] and ulnae I mention above. What
    arboreal bipedal species do you know with these features?

    All, in a spectrum, Homo at one end, arboreals the other.
    I am hard-pressed to describe extant humans as arboreal bipeds.

    Probable part-time arboreal bipeds: Homo habilis, georgicus, naledi, florensis, etc.
    So you don't mean H.sapiens or H. neanderthalensis.
    They are at the far end. Rainforest H&G do climb trees seeking seasonal foods, fruits, honey, nuts, and during war hide in tree nests, but otherwise are terrestrial. Neanderthals may have hunted from treestands. No Homo had a divergent hallux.
    I've seen many young men climb coconut palms in SEAsia w/o tools, just takes practice & thirst.
    I am hard-pressed to describe tree-climbing as arboreal bipedalism, especially the way those young men climb coconut palms.

    I watched my buddy climb swiftly (for a human) up a coconut palm, using his hands in (bimanual) tension and feet in (bipedal) compression, at the top of the stem, he spun off and dropped a half dozen nuts, then climbed down. That is one form of arboreal
    bipedalism. Tswa pygmies climb tall trees by using neighboring small trees to start up, then bridge over to horizontal branches which they then walk on, using hands in tension, feet in compression. Monkeys doing the same switch to quadrupedalism, hands
    and feet in compression on horizontal branches.

    Human
    are likely descended from arboreal bipeds, but it's a derived
    characteristic.
    Extant knucklewalking apes which sleep in bowl nests? Humans are gracile terrestrial bipeds.
    Not even mentioned: gibbons and humans share long achilles tendon and long lower back, opposite of extant great apes.
    Do the cited papers mention these things? If not, that would explain
    why Erika doesn't either.

    *Human bipedalism* cannot be *explained* without it. (It can be discussed & lectured, but not explained.) Picking out a few unique features and ignoring others doesn't explain anything.

    There's also this: https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-022-08828-7
    Not sure what chromosome 2 fusion has to do with this topic. Please >> >> >> elaborate.
    H/P split estimated timing .9ma is much later than MSC (Medit. & Red Sea dried out); H erectus bridged the est. date, so would have had 24, not 23 like Hs. I doubt their estimate.
    I acknowledge that chromosome 2 distinguishes extant humans from all >> >> other extant apes, and that the most parsimonious explanation is that >> >> the fusion event happened after the LCA of humans and other extant
    apes.

    Rather, during, imo.
    Of course it's possible the fusion event coincidentally happened
    during LCA, but less likely and not necessary.
    Uncertain, but I think there was causation. The chr 2 fusion also partly inverted the script, a rare thing; which I think produced speciation. No Homo is known to have 24/48 chromosomes.
    I acknowledge the fusion event inverted part of chromosome 2. However,
    that didn't alter how genes are transcribed.

    All great apes have 24, all humans have 23 pairs (except Downs syndrome etc.). The method of transcription is irrelevant, the *result* is speciation, no known exception, a genetic firewall.
    Like hylobatids, humans do not have 24 pairs of chromosomes, nor sleep in arboreal bowl nests, nor have short backs, nor short legs. Like hylobatids, we have relatively long legs, walk upright and use hands to grasp tensionally.
    My conjecture stands.

    By the way, the video transcripts are cringeworthy. Hard to believe they are processed by a company called Alphabet, google-youtube's parent company. I expected far better performance from them.

    This is a common
    misconception. For any given DNA sequence, there is a 5-prime end and
    a 3-prime end. Transcription from DNA to mRNA always starts from the
    5-prime end and ends at the 3-prime end:

    <https://www.thoughtco.com/steps-of-transcription-from-dna-to-rna-603895>
    The chromosome 2
    fusion wouldn't have caused any loss of genetic information or a
    speciation event, at least not initially. So it's more likely to have
    happened somewhere between 4 mya and 0.9 mya.
    I'll stick with my conjecture.
    Some molecular biology might help unstick you from your conjecture.
    According to this:
    <https://en.wikipedia.org/wiki/Hominini>

    LCA of gibbons and humans existed around 15.7 mya.
    LCA of orangs and humans existed around 8.8 mya.
    LCA of gorillas and humans existed around 6.3 mya.
    LCA of chimpanzees and humans existed some time after that, with no
    specified date. I have read other articles which suggest 4 mya.

    So your cited paper's estimated date for the fusion event of 0.9 mya >> >> is well after those dates. I agree that sounds very recent, but
    either way doesn't inform when the human lineage first began
    terrestrial bipedalism.

    True.

    As Erika points out, arboreal bipedalism can
    be precursor to both knuckle-walking and human terrestrial bipedalism. >> >
    Yes, of course. Can & was, alongside arboreal bimanualism (slow brachiation).

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to daud.deden@gmail.com on Sun Oct 30 22:20:33 2022
    On Sun, 30 Oct 2022 16:58:57 -0700 (PDT), Daud Deden
    <daud.deden@gmail.com> wrote:

    On Sunday, October 30, 2022 at 5:17:46 PM UTC-4, 69jp...@gmail.com wrote:
    On Sun, 30 Oct 2022 09:52:58 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Sunday, October 30, 2022 at 10:46:43 AM UTC-4, 69jp...@gmail.com wrote: >> <snip uncommented text for brevity>
    but I suspect she's referring to
    the 4 anatomical features of the tibia [femur] and ulnae I mention above. What
    arboreal bipedal species do you know with these features?

    All, in a spectrum, Homo at one end, arboreals the other.
    I am hard-pressed to describe extant humans as arboreal bipeds.

    Probable part-time arboreal bipeds: Homo habilis, georgicus, naledi, florensis, etc.
    So you don't mean H.sapiens or H. neanderthalensis.
    They are at the far end. Rainforest H&G do climb trees seeking seasonal foods, fruits, honey, nuts, and during war hide in tree nests, but otherwise are terrestrial. Neanderthals may have hunted from treestands. No Homo had a divergent hallux.
    I've seen many young men climb coconut palms in SEAsia w/o tools, just takes practice & thirst.
    I am hard-pressed to describe tree-climbing as arboreal bipedalism,
    especially the way those young men climb coconut palms.

    I watched my buddy climb swiftly (for a human) up a coconut palm, using his hands in (bimanual) tension and feet in (bipedal) compression, at the top of the stem, he spun off and dropped a half dozen nuts, then climbed down. That is one form of arboreal
    bipedalism. Tswa pygmies climb tall trees by using neighboring small trees to start up, then bridge over to horizontal branches which they then walk on, using hands in tension, feet in compression. Monkeys doing the same switch to quadrupedalism, hands
    and feet in compression on horizontal branches.

    Human
    are likely descended from arboreal bipeds, but it's a derived
    characteristic.
    Extant knucklewalking apes which sleep in bowl nests? Humans are gracile terrestrial bipeds.
    Not even mentioned: gibbons and humans share long achilles tendon and long lower back, opposite of extant great apes.
    Do the cited papers mention these things? If not, that would explain
    why Erika doesn't either.

    *Human bipedalism* cannot be *explained* without it. (It can be discussed & lectured, but not explained.) Picking out a few unique features and ignoring others doesn't explain anything.

    There's also this: https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-022-08828-7
    Not sure what chromosome 2 fusion has to do with this topic. Please
    elaborate.
    H/P split estimated timing .9ma is much later than MSC (Medit. & Red Sea dried out); H erectus bridged the est. date, so would have had 24, not 23 like Hs. I doubt their estimate.
    I acknowledge that chromosome 2 distinguishes extant humans from all >> >> >> other extant apes, and that the most parsimonious explanation is that >> >> >> the fusion event happened after the LCA of humans and other extant
    apes.

    Rather, during, imo.
    Of course it's possible the fusion event coincidentally happened
    during LCA, but less likely and not necessary.
    Uncertain, but I think there was causation. The chr 2 fusion also partly inverted the script, a rare thing; which I think produced speciation. No Homo is known to have 24/48 chromosomes.
    I acknowledge the fusion event inverted part of chromosome 2. However,
    that didn't alter how genes are transcribed.

    All great apes have 24, all humans have 23 pairs (except Downs syndrome etc.). >The method of transcription is irrelevant, the *result* is speciation, no known exception, a genetic firewall.
    Like hylobatids, humans do not have 24 pairs of chromosomes, nor sleep in arboreal bowl nests, nor have short backs, nor short legs. Like hylobatids, we have relatively long legs, walk upright and use hands to grasp tensionally.
    My conjecture stands.


    You're entitled to your opinion.


    By the way, the video transcripts are cringeworthy. Hard to believe they are processed by a company called Alphabet, google-youtube's parent company. I expected far better performance from them.

    This is a common
    misconception. For any given DNA sequence, there is a 5-prime end and
    a 3-prime end. Transcription from DNA to mRNA always starts from the
    5-prime end and ends at the 3-prime end:

    <https://www.thoughtco.com/steps-of-transcription-from-dna-to-rna-603895>
    The chromosome 2
    fusion wouldn't have caused any loss of genetic information or a
    speciation event, at least not initially. So it's more likely to have
    happened somewhere between 4 mya and 0.9 mya.
    I'll stick with my conjecture.
    Some molecular biology might help unstick you from your conjecture.
    According to this:
    <https://en.wikipedia.org/wiki/Hominini>

    LCA of gibbons and humans existed around 15.7 mya.
    LCA of orangs and humans existed around 8.8 mya.
    LCA of gorillas and humans existed around 6.3 mya.
    LCA of chimpanzees and humans existed some time after that, with no >> >> >> specified date. I have read other articles which suggest 4 mya.

    So your cited paper's estimated date for the fusion event of 0.9 mya >> >> >> is well after those dates. I agree that sounds very recent, but
    either way doesn't inform when the human lineage first began
    terrestrial bipedalism.

    True.

    As Erika points out, arboreal bipedalism can
    be precursor to both knuckle-walking and human terrestrial bipedalism.

    Yes, of course. Can & was, alongside arboreal bimanualism (slow brachiation).

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Sun Oct 30 21:59:15 2022
    On Sunday, October 30, 2022 at 10:20:34 PM UTC-4, 69jp...@gmail.com wrote:
    On Sun, 30 Oct 2022 16:58:57 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Sunday, October 30, 2022 at 5:17:46 PM UTC-4, 69jp...@gmail.com wrote: >> On Sun, 30 Oct 2022 09:52:58 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Sunday, October 30, 2022 at 10:46:43 AM UTC-4, 69jp...@gmail.com wrote:
    <snip uncommented text for brevity>
    but I suspect she's referring to
    the 4 anatomical features of the tibia [femur] and ulnae I mention above. What
    arboreal bipedal species do you know with these features?

    All, in a spectrum, Homo at one end, arboreals the other.
    I am hard-pressed to describe extant humans as arboreal bipeds.

    Probable part-time arboreal bipeds: Homo habilis, georgicus, naledi, florensis, etc.
    So you don't mean H.sapiens or H. neanderthalensis.
    They are at the far end. Rainforest H&G do climb trees seeking seasonal foods, fruits, honey, nuts, and during war hide in tree nests, but otherwise are terrestrial. Neanderthals may have hunted from treestands. No Homo had a divergent hallux.
    I've seen many young men climb coconut palms in SEAsia w/o tools, just takes practice & thirst.
    I am hard-pressed to describe tree-climbing as arboreal bipedalism,
    especially the way those young men climb coconut palms.

    I watched my buddy climb swiftly (for a human) up a coconut palm, using his hands in (bimanual) tension and feet in (bipedal) compression, at the top of the stem, he spun off and dropped a half dozen nuts, then climbed down. That is one form of
    arboreal bipedalism. Tswa pygmies climb tall trees by using neighboring small trees to start up, then bridge over to horizontal branches which they then walk on, using hands in tension, feet in compression. Monkeys doing the same switch to quadrupedalism,
    hands and feet in compression on horizontal branches.

    Human
    are likely descended from arboreal bipeds, but it's a derived
    characteristic.
    Extant knucklewalking apes which sleep in bowl nests? Humans are gracile terrestrial bipeds.
    Not even mentioned: gibbons and humans share long achilles tendon and long lower back, opposite of extant great apes.
    Do the cited papers mention these things? If not, that would explain
    why Erika doesn't either.

    *Human bipedalism* cannot be *explained* without it. (It can be discussed & lectured, but not explained.) Picking out a few unique features and ignoring others doesn't explain anything.

    There's also this: https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-022-08828-7
    Not sure what chromosome 2 fusion has to do with this topic. Please
    elaborate.
    H/P split estimated timing .9ma is much later than MSC (Medit. & Red Sea dried out); H erectus bridged the est. date, so would have had 24, not 23 like Hs. I doubt their estimate.
    I acknowledge that chromosome 2 distinguishes extant humans from all
    other extant apes, and that the most parsimonious explanation is that
    the fusion event happened after the LCA of humans and other extant >> >> >> apes.

    Rather, during, imo.
    Of course it's possible the fusion event coincidentally happened
    during LCA, but less likely and not necessary.
    Uncertain, but I think there was causation. The chr 2 fusion also partly inverted the script, a rare thing; which I think produced speciation. No Homo is known to have 24/48 chromosomes.
    I acknowledge the fusion event inverted part of chromosome 2. However,
    that didn't alter how genes are transcribed.

    All great apes have 24, all humans have 23 pairs (except Downs syndrome etc.).
    The method of transcription is irrelevant, the *result* is speciation, no known exception, a genetic firewall.
    Like hylobatids, humans do not have 24 pairs of chromosomes, nor sleep in arboreal bowl nests, nor have short backs, nor short legs. Like hylobatids, we have relatively long legs, walk upright and use hands to grasp tensionally.
    My conjecture stands.
    You're entitled to your opinion.
    And you yours.
    By the way, the video transcripts are cringeworthy. Hard to believe they are processed by a company called Alphabet, google-youtube's parent company. I expected far better performance from them.

    This is a common
    misconception. For any given DNA sequence, there is a 5-prime end and
    a 3-prime end. Transcription from DNA to mRNA always starts from the
    5-prime end and ends at the 3-prime end:

    <https://www.thoughtco.com/steps-of-transcription-from-dna-to-rna-603895> >> >> The chromosome 2
    fusion wouldn't have caused any loss of genetic information or a
    speciation event, at least not initially. So it's more likely to have >> >> happened somewhere between 4 mya and 0.9 mya.
    I'll stick with my conjecture.
    Some molecular biology might help unstick you from your conjecture.
    According to this:
    <https://en.wikipedia.org/wiki/Hominini>

    LCA of gibbons and humans existed around 15.7 mya.
    LCA of orangs and humans existed around 8.8 mya.
    LCA of gorillas and humans existed around 6.3 mya.
    LCA of chimpanzees and humans existed some time after that, with no >> >> >> specified date. I have read other articles which suggest 4 mya.

    So your cited paper's estimated date for the fusion event of 0.9 mya
    is well after those dates. I agree that sounds very recent, but
    either way doesn't inform when the human lineage first began
    terrestrial bipedalism.

    True.

    As Erika points out, arboreal bipedalism can
    be precursor to both knuckle-walking and human terrestrial bipedalism.

    Yes, of course. Can & was, alongside arboreal bimanualism (slow brachiation).

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to daud.deden@gmail.com on Mon Oct 31 02:04:18 2022
    On Sun, 30 Oct 2022 21:59:15 -0700 (PDT), Daud Deden
    <daud.deden@gmail.com> wrote:

    On Sunday, October 30, 2022 at 10:20:34 PM UTC-4, 69jp...@gmail.com wrote:
    On Sun, 30 Oct 2022 16:58:57 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Sunday, October 30, 2022 at 5:17:46 PM UTC-4, 69jp...@gmail.com wrote: >> >> On Sun, 30 Oct 2022 09:52:58 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Sunday, October 30, 2022 at 10:46:43 AM UTC-4, 69jp...@gmail.com wrote:
    <snip uncommented text for brevity>
    but I suspect she's referring to
    the 4 anatomical features of the tibia [femur] and ulnae I mention above. What
    arboreal bipedal species do you know with these features?

    All, in a spectrum, Homo at one end, arboreals the other.
    I am hard-pressed to describe extant humans as arboreal bipeds.

    Probable part-time arboreal bipeds: Homo habilis, georgicus, naledi, florensis, etc.
    So you don't mean H.sapiens or H. neanderthalensis.
    They are at the far end. Rainforest H&G do climb trees seeking seasonal foods, fruits, honey, nuts, and during war hide in tree nests, but otherwise are terrestrial. Neanderthals may have hunted from treestands. No Homo had a divergent hallux.
    I've seen many young men climb coconut palms in SEAsia w/o tools, just takes practice & thirst.
    I am hard-pressed to describe tree-climbing as arboreal bipedalism,
    especially the way those young men climb coconut palms.

    I watched my buddy climb swiftly (for a human) up a coconut palm, using his hands in (bimanual) tension and feet in (bipedal) compression, at the top of the stem, he spun off and dropped a half dozen nuts, then climbed down. That is one form of
    arboreal bipedalism. Tswa pygmies climb tall trees by using neighboring small trees to start up, then bridge over to horizontal branches which they then walk on, using hands in tension, feet in compression. Monkeys doing the same switch to quadrupedalism,
    hands and feet in compression on horizontal branches.

    Human
    are likely descended from arboreal bipeds, but it's a derived
    characteristic.
    Extant knucklewalking apes which sleep in bowl nests? Humans are gracile terrestrial bipeds.
    Not even mentioned: gibbons and humans share long achilles tendon and long lower back, opposite of extant great apes.
    Do the cited papers mention these things? If not, that would explain
    why Erika doesn't either.

    *Human bipedalism* cannot be *explained* without it. (It can be discussed & lectured, but not explained.) Picking out a few unique features and ignoring others doesn't explain anything.

    There's also this: https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-022-08828-7
    Not sure what chromosome 2 fusion has to do with this topic. Please
    elaborate.
    H/P split estimated timing .9ma is much later than MSC (Medit. & Red Sea dried out); H erectus bridged the est. date, so would have had 24, not 23 like Hs. I doubt their estimate.
    I acknowledge that chromosome 2 distinguishes extant humans from all
    other extant apes, and that the most parsimonious explanation is that
    the fusion event happened after the LCA of humans and other extant >> >> >> >> apes.

    Rather, during, imo.
    Of course it's possible the fusion event coincidentally happened
    during LCA, but less likely and not necessary.
    Uncertain, but I think there was causation. The chr 2 fusion also partly inverted the script, a rare thing; which I think produced speciation. No Homo is known to have 24/48 chromosomes.
    I acknowledge the fusion event inverted part of chromosome 2. However, >> >> that didn't alter how genes are transcribed.

    All great apes have 24, all humans have 23 pairs (except Downs syndrome etc.).
    The method of transcription is irrelevant, the *result* is speciation, no known exception, a genetic firewall.
    Like hylobatids, humans do not have 24 pairs of chromosomes, nor sleep in arboreal bowl nests, nor have short backs, nor short legs. Like hylobatids, we have relatively long legs, walk upright and use hands to grasp tensionally.
    My conjecture stands.
    You're entitled to your opinion.
    And you yours.


    So that's something else we agree about.


    By the way, the video transcripts are cringeworthy. Hard to believe they are processed by a company called Alphabet, google-youtube's parent company. I expected far better performance from them.

    This is a common
    misconception. For any given DNA sequence, there is a 5-prime end and
    a 3-prime end. Transcription from DNA to mRNA always starts from the
    5-prime end and ends at the 3-prime end:

    <https://www.thoughtco.com/steps-of-transcription-from-dna-to-rna-603895>
    The chromosome 2
    fusion wouldn't have caused any loss of genetic information or a
    speciation event, at least not initially. So it's more likely to have >> >> >> happened somewhere between 4 mya and 0.9 mya.
    I'll stick with my conjecture.
    Some molecular biology might help unstick you from your conjecture.
    According to this:
    <https://en.wikipedia.org/wiki/Hominini>

    LCA of gibbons and humans existed around 15.7 mya.
    LCA of orangs and humans existed around 8.8 mya.
    LCA of gorillas and humans existed around 6.3 mya.
    LCA of chimpanzees and humans existed some time after that, with no
    specified date. I have read other articles which suggest 4 mya.

    So your cited paper's estimated date for the fusion event of 0.9 mya
    is well after those dates. I agree that sounds very recent, but
    either way doesn't inform when the human lineage first began
    terrestrial bipedalism.

    True.

    As Erika points out, arboreal bipedalism can
    be precursor to both knuckle-walking and human terrestrial bipedalism.

    Yes, of course. Can & was, alongside arboreal bimanualism (slow brachiation).

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Mon Oct 31 03:06:42 2022
    On Monday, October 31, 2022 at 2:04:19 AM UTC-4, 69jp...@gmail.com wrote:
    On Sun, 30 Oct 2022 21:59:15 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Sunday, October 30, 2022 at 10:20:34 PM UTC-4, 69jp...@gmail.com wrote: >> On Sun, 30 Oct 2022 16:58:57 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Sunday, October 30, 2022 at 5:17:46 PM UTC-4, 69jp...@gmail.com wrote:
    On Sun, 30 Oct 2022 09:52:58 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Sunday, October 30, 2022 at 10:46:43 AM UTC-4, 69jp...@gmail.com wrote:
    <snip uncommented text for brevity>
    but I suspect she's referring to
    the 4 anatomical features of the tibia [femur] and ulnae I mention above. What
    arboreal bipedal species do you know with these features?

    All, in a spectrum, Homo at one end, arboreals the other.
    I am hard-pressed to describe extant humans as arboreal bipeds. >> >> >> >
    Probable part-time arboreal bipeds: Homo habilis, georgicus, naledi, florensis, etc.
    So you don't mean H.sapiens or H. neanderthalensis.
    They are at the far end. Rainforest H&G do climb trees seeking seasonal foods, fruits, honey, nuts, and during war hide in tree nests, but otherwise are terrestrial. Neanderthals may have hunted from treestands. No Homo had a divergent hallux.
    I've seen many young men climb coconut palms in SEAsia w/o tools, just takes practice & thirst.
    I am hard-pressed to describe tree-climbing as arboreal bipedalism,
    especially the way those young men climb coconut palms.

    I watched my buddy climb swiftly (for a human) up a coconut palm, using his hands in (bimanual) tension and feet in (bipedal) compression, at the top of the stem, he spun off and dropped a half dozen nuts, then climbed down. That is one form of
    arboreal bipedalism. Tswa pygmies climb tall trees by using neighboring small trees to start up, then bridge over to horizontal branches which they then walk on, using hands in tension, feet in compression. Monkeys doing the same switch to quadrupedalism,
    hands and feet in compression on horizontal branches.

    Human
    are likely descended from arboreal bipeds, but it's a derived
    characteristic.
    Extant knucklewalking apes which sleep in bowl nests? Humans are gracile terrestrial bipeds.
    Not even mentioned: gibbons and humans share long achilles tendon and long lower back, opposite of extant great apes.
    Do the cited papers mention these things? If not, that would explain
    why Erika doesn't either.

    *Human bipedalism* cannot be *explained* without it. (It can be discussed & lectured, but not explained.) Picking out a few unique features and ignoring others doesn't explain anything.

    There's also this: https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-022-08828-7
    Not sure what chromosome 2 fusion has to do with this topic. Please
    elaborate.
    H/P split estimated timing .9ma is much later than MSC (Medit. & Red Sea dried out); H erectus bridged the est. date, so would have had 24, not 23 like Hs. I doubt their estimate.
    I acknowledge that chromosome 2 distinguishes extant humans from all
    other extant apes, and that the most parsimonious explanation is that
    the fusion event happened after the LCA of humans and other extant
    apes.

    Rather, during, imo.
    Of course it's possible the fusion event coincidentally happened
    during LCA, but less likely and not necessary.
    Uncertain, but I think there was causation. The chr 2 fusion also partly inverted the script, a rare thing; which I think produced speciation. No Homo is known to have 24/48 chromosomes.
    I acknowledge the fusion event inverted part of chromosome 2. However, >> >> that didn't alter how genes are transcribed.

    All great apes have 24, all humans have 23 pairs (except Downs syndrome etc.).
    The method of transcription is irrelevant, the *result* is speciation, no known exception, a genetic firewall.
    Like hylobatids, humans do not have 24 pairs of chromosomes, nor sleep in arboreal bowl nests, nor have short backs, nor short legs. Like hylobatids, we have relatively long legs, walk upright and use hands to grasp tensionally.
    My conjecture stands.
    You're entitled to your opinion.
    And you yours.
    So that's something else we agree about.
    Coincidence, perhaps.
    By the way, the video transcripts are cringeworthy. Hard to believe they are processed by a company called Alphabet, google-youtube's parent company. I expected far better performance from them.

    This is a common
    misconception. For any given DNA sequence, there is a 5-prime end and >> >> a 3-prime end. Transcription from DNA to mRNA always starts from the >> >> 5-prime end and ends at the 3-prime end:

    <https://www.thoughtco.com/steps-of-transcription-from-dna-to-rna-603895>
    The chromosome 2
    fusion wouldn't have caused any loss of genetic information or a
    speciation event, at least not initially. So it's more likely to have
    happened somewhere between 4 mya and 0.9 mya.
    I'll stick with my conjecture.
    Some molecular biology might help unstick you from your conjecture.
    According to this:
    <https://en.wikipedia.org/wiki/Hominini>

    LCA of gibbons and humans existed around 15.7 mya.
    LCA of orangs and humans existed around 8.8 mya.
    LCA of gorillas and humans existed around 6.3 mya.
    LCA of chimpanzees and humans existed some time after that, with no
    specified date. I have read other articles which suggest 4 mya. >> >> >> >>
    So your cited paper's estimated date for the fusion event of 0.9 mya
    is well after those dates. I agree that sounds very recent, but >> >> >> >> either way doesn't inform when the human lineage first began
    terrestrial bipedalism.

    True.

    As Erika points out, arboreal bipedalism can
    be precursor to both knuckle-walking and human terrestrial bipedalism.

    Yes, of course. Can & was, alongside arboreal bimanualism (slow brachiation).

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Mon Oct 31 15:15:01 2022
    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY

    At 3:40 she talks about different modes of arboreal locomotion...she mentions "generalized miocene ape" & similar to "palmigrade pronograde arboreal quadrupeds of the miocene'.
    To me, the European miocene apes were arboreal slow bimanual brachiating & slow upright bipedal walking on horizontal tree branches.
    Is she referring to African miocene apes being pronograde palmigrade?

    At 7:20, she apparently claims that chimp and gorilla arboreal traits interfere with their terrestrial locomotion "act to negate bipedalism" No, sleeping in bowl nests did that, selecting for short legs & backs.
    https://youtu.be/jo2ZLnucuHY?t=451

    I wanted to go in depth on this video, but there is a massive noisy halloween celebration of trick or treating goblins and princesses here at the library. So enough.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Peter Nyikos@21:1/5 to where I elaborated a bit on what I on Mon Oct 31 17:50:26 2022
    On Sunday, October 30, 2022 at 12:11:42 PM UTC-4, Trolidan7 wrote:
    On 10/27/22 7:26 PM, Peter Nyikos wrote:
    On Tuesday, October 25, 2022 at 4:18:31 AM UTC-4, Trolidan7 wrote:
    On 10/23/22 11:50 PM, jillery wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several >>> papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several >>> hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.

    I tend to think of it as none of the above.

    Did you watch the video, to see what they were?

    I did watch nearly all of both.

    I watched both over the weekend, and even did a comment to the one on bipedalism,
    where I elaborated a bit on what I wrote below about the bipedal lemurs.


    In general she studied questions about the nature
    of the environmental factors that may have produced
    bipedalism rather than the factors involving the
    specific dynamics of walking.

    I once partially remember a teacher a long time
    ago saying science does not ask 'why' questions.

    I argued that one could rephrase questions so
    that they were essentially the same either using
    or not using the word 'why'.

    Yes. Later this week, I will be starting a thread titled something like:

    "Which mammals and birds survived the great K-T extinction, and why?"

    You might think "how" could be substituted for "why," but it does not
    lead so easily into talking about why other species perished.


    Reasonably, if
    the question is short enough it can have an array
    of meanings and what is referred to can be unclear.

    This was about 30 years ago and it would take a while
    to remember which specific class or subject.

    About 'blood and lymph' and the nature of where
    copper is on a cellular and extracellular level
    in invertebrates and giving a reference I am also
    sorry. It could take an incredible amount of digging
    to find where and when I read that and I could still
    be off when it comes to precisely when or where I
    might have done that. I could be way off.

    As the Aussies say, "No worries, mate."


    For the video I did that a few days ago.

    Granted, with an open-ended subject like bipedalism, it is quite
    unlikely that any "why" that we humans can easily formulate
    gives a reason that is anywhere near complete.

    Erika says something like this in her video, but then she gives
    what she thinks is the dominant reason.


    It's almost as bad as theories about how we developed such amazingly sophisticated speech. Simplified theories have been
    given derisive names like "bow-wow theory" and "ding-dong theory"
    or even been accused of being "pseudoscientific."

    Simply because it is not that easy to stand upright.

    When an animal stands upright you need to solve a problem -
    how do you keep from falling over forward and backward.

    This might seem simple but it is not because with a four
    footed animal the center of gravity forward and backward
    is between the front legs and the back legs, and often
    that is a greater distance than between the left legs and
    the right legs.

    Some animals that sort of walk on twos have not solved the
    problem - a kangaroo can hop but in general it can not
    stably stand.

    On the other hand, sifakas, the avahi, and the indri -- all lemurs -- are even more
    obligate bipedal than we are: their forelimbs are even shorter
    in proportion to their hindlimbs than ours are.

    Their primary way of getting from one place to another
    is fully bipedal hopping, generally between trees.
    However, I have a book with a photograph
    in which a sifaka has a very typically human style
    running pose, with arms swinging in opposite
    orientation to her wide-apart (from front to back) legs.

    She gave the idea that the apes may have once been
    more bipedal, and then specialized for four legged
    walking in chimps and gorillas and specialized for
    bipedal walking in humans, and she did not specify
    precisely what she was referring to. What you
    are typing, however, may have parallels in natural
    history that are what she is referring to.

    The kind of bipedalism displayed by these lemurs, even though it takes place in trees,
    is different from the kind Erika talked about in her favored theory.
    So the transition to walking and running on the ground used by the sifaka I mentioned
    is yet another possible transition to the kind of walking and running in which our
    remote ancestors came to adopt.


    Often the word 'walking' tends to imply locomotion
    on the ground, but when you are climbing up, down,
    or across a tree it can in some ways be motion
    across a different substrate, just as 'swimming',
    'walking', are 'flying' can often be thought of
    as different things, involving substrates of liquid,
    a solid ground, or air.

    An example I talked about with John Harshman on another thread
    is that penguins "fly" through water using their "wings" as
    the main form of propulsion.

    Are we obligate bipeds? For humans, it is possible
    to crawl but that is rare. That tends to be most
    commonly used. Do many apes or monkeys have four
    'hands'? Often we tend to use the word 'hand' for
    a limb that tends to manipulate objects, and 'wing'
    for one that tends to fly. But if an animal is
    moving by transferring to different locations on
    or between trees, then the boundary between 'moving'
    and 'manipulating objects' may be blurred.

    Yes, like manipulating branches while slowly making
    one's way through dense foliage.


    It was several days ago, and I would have to rewatch
    it again to summarize the different theories that
    she gave and the specific one that she supported.

    I saw it more recently, but I'd have to watch it again
    to really understand the one that she supported.
    The other two, environmental pressure due to forests being
    replaced by savannas, and wading frequently in water,
    are easy to describe in comparison.

    Admittedly, it was generally a different question.

    Either way, in essence, the long hand enables
    force to be supplied >> to the far front and far back to counter
    falling forward or backward - the forefoot and big toe are
    the front force appliers and the heel is the back force
    applier. Then of course there are some animals that might
    sort of walk on threes (I am thinking of the Jerboa) - but
    humans have an extra problem because they have no tail to
    possibly act as an extra walking limb, or at least a balance.

    Indris have almost lost their tails, but you've made me wonder
    whether the long, narrow tail of that sifaka was an aid in
    balancing, making that human-like stride possible.

    And, like a bicyclist may use training wheels while learning how to
    properly pedal, and then remove them, so the tail might come to shrink,
    given a few million years, as one lineage of sifakas take more and
    more to walking/running rather than hopping with both feet at a time.

    This makes me wonder how much monkeys changed their movements
    as they gradually lost their tails to become apes.


    Peter Nyikos
    Professor, Dept. of Mathematics -- standard disclaimer--
    Univ. of South Carolina in Columbia
    http://people.math.sc.edu/nyikos

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to daud.deden@gmail.com on Tue Nov 1 04:17:27 2022
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud.deden@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY


    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy.


    At 3:40 she talks about different modes of arboreal locomotion...she mentions "generalized miocene ape" & similar to "palmigrade pronograde arboreal quadrupeds of the miocene'.
    To me, the European miocene apes were arboreal slow bimanual brachiating & slow upright bipedal walking on horizontal tree branches.
    Is she referring to African miocene apes being pronograde palmigrade?


    Erika says this:
    *********************************
    Obviously australopithecus afarensis didn't evolve from a chimp but
    from sort of generalized Miocene ape. But that being said, the
    morphology of modern chimpanzees is at least similar to some of our
    palmigrade pronograde arboreal quadrupeds of the Miocene. *********************************

    So yes, Erika is saying at least some African Miocene apes were
    palmigrade aka foot parallel to the ground pronograde aka spine
    parallel to the ground, similar to modern chimpanzees.

    I don't know enough about Miocene apes to say if European and African
    apes were different. My understanding is climate change caused
    European Miocene apes to go extinct before Australopiths evolved in
    Africa, which suggests to me the two environments were different
    enough to support the differences you describe.


    At 7:20, she apparently claims that chimp and gorilla arboreal traits interfere with their terrestrial locomotion "act to negate bipedalism" No, sleeping in bowl nests did that, selecting for short legs & backs.
    https://youtu.be/jo2ZLnucuHY?t=451


    Erika says this:
    ***********************************************
    Either way, the aspects that allow for arboriality found in
    australopithecus afarensis are not the same types as the ones that we
    find in chimpanzees and gorillas. In the latter two species, the
    arboreal aspects act to negate efficient bipedality, whereas in australopithecus afarensis they're sort of removed from it. They
    allow for arboreal behaviors when necessary but don't
    harm the effectiveness of bipedality when the animal came down to the
    ground.
    *********************************************

    Erika doesn't argue the cause for these arboreal aspects, but only
    that their presence in chimpanzees and gorillas inhibits efficient
    bipedality. Anybody who has seen videos of gorillas and chimpanzees
    walking bipedally would agree they are much less efficient at it than
    are humans. Erika's point in paraphrase is that Lucy had a big butt, I
    cannot lie, and so walked more like humans do.



    I wanted to go in depth on this video, but there is a massive noisy halloween celebration of trick or treating goblins and princesses here at the library. So enough.


    I hope you find time once the ghosts and goblins have gone.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Wed Nov 2 15:39:00 2022
    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy.
    At 3:40 she talks about different modes of arboreal locomotion...she mentions "generalized miocene ape" & similar to "palmigrade pronograde arboreal quadrupeds of the miocene'.
    To me, the European miocene apes were arboreal slow bimanual brachiating & slow upright bipedal walking on horizontal tree branches.
    Is she referring to African miocene apes being pronograde palmigrade?
    Erika says this:
    *********************************
    Obviously australopithecus afarensis didn't evolve from a chimp but
    from sort of generalized Miocene ape. But that being said, the
    morphology of modern chimpanzees is at least similar to some of our palmigrade pronograde arboreal quadrupeds of the Miocene. *********************************

    So yes, Erika is saying at least some African Miocene apes were
    palmigrade aka foot parallel to the ground pronograde aka spine
    parallel to the ground, similar to modern chimpanzees.

    I don't know enough about Miocene apes to say if European and African
    apes were different. My understanding is climate change caused
    European Miocene apes to go extinct before Australopiths evolved in
    Africa, which suggests to me the two environments were different
    enough to support the differences you describe.
    At 7:20, she apparently claims that chimp and gorilla arboreal traits interfere with their terrestrial locomotion "act to negate bipedalism" No, sleeping in bowl nests did that, selecting for short legs & backs.
    https://youtu.be/jo2ZLnucuHY?t=451
    Erika says this:
    ***********************************************
    Either way, the aspects that allow for arboriality found in
    australopithecus afarensis are not the same types as the ones that we
    find in chimpanzees and gorillas. In the latter two species, the
    arboreal aspects act to negate efficient bipedality, whereas in australopithecus afarensis they're sort of removed from it. They
    allow for arboreal behaviors when necessary but don't
    harm the effectiveness of bipedality when the animal came down to the
    ground.
    *********************************************

    Erika doesn't argue the cause for these arboreal aspects, but only
    that their presence in chimpanzees and gorillas inhibits efficient bipedality. Anybody who has seen videos of gorillas and chimpanzees
    walking bipedally would agree they are much less efficient at it than
    are humans. Erika's point in paraphrase is that Lucy had a big butt, I
    cannot lie, and so walked more like humans do.
    I wanted to go in depth on this video, but there is a massive noisy halloween celebration of trick or treating goblins and princesses here at the library. So enough.
    I hope you find time once the ghosts and goblins have gone.

    All gone, library quiet today. Unfortunately, it closes in a few minutes, so will write later.
    Found Erika's video on new fossil gibbon, 7-8ma, interesting. https://www.youtube.com/watch?v=zCJH1O1Rpw8&list=RDCMUCJNcAH2yzV3VAMYIGxCZ8_w&index=4

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Thu Nov 3 07:56:05 2022
    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote: >> Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.

    At 3:40 she talks about different modes of arboreal locomotion...she mentions "generalized miocene ape" & similar to "palmigrade pronograde arboreal quadrupeds of the miocene'.
    To me, the European miocene apes were arboreal slow bimanual brachiating & slow upright bipedal walking on horizontal tree branches.
    Is she referring to African miocene apes being pronograde palmigrade?
    Erika says this:
    *********************************
    Obviously australopithecus afarensis didn't evolve from a chimp but
    from sort of generalized Miocene ape. But that being said, the
    morphology of modern chimpanzees is at least similar to some of our palmigrade pronograde arboreal quadrupeds of the Miocene. *********************************

    So yes, Erika is saying at least some African Miocene apes were
    palmigrade aka foot parallel to the ground pronograde aka spine
    parallel to the ground, similar to modern chimpanzees.

    Chimps aren't palmigrade, no extant ape is, all monkeys are obligatory palmigrade. Humans are palmigrade only during infancy while knee-crawling and bear-walking (I'd guess only within a dome shelter). Humans and chimps hold tools in hands, but that's
    different from palmigrady.

    I don't know enough about Miocene apes to say if European and African
    apes were different. My understanding is climate change caused
    European Miocene apes to go extinct before Australopiths evolved in
    Africa, which suggests to me the two environments were different
    enough to support the differences you describe.

    I opine that European Miocene apes expanded from the Black Sea region after the MSC, some of their descendants included australopiths, Homo etc. entering Africa in waves.

    At 7:20, she apparently claims that chimp and gorilla arboreal traits interfere with their terrestrial locomotion "act to negate bipedalism" No, sleeping in bowl nests did that, selecting for short legs & backs.
    https://youtu.be/jo2ZLnucuHY?t=451
    Erika says this:
    ***********************************************
    Either way, the aspects that allow for arboriality found in
    australopithecus afarensis are not the same types as the ones that we
    find in chimpanzees and gorillas. In the latter two species, the
    arboreal aspects

    I guess 'aspect' could include arboreal bowl nesting, I thought she meant arboreal locomotion only.

    act to negate efficient bipedality,

    Not arboreal hylobatids. Bowl sleeping in great apes shrank their leg, achilles & back length.

    whereas in
    australopithecus afarensis they're sort of removed from it.

    The key is whether australopiths & kin had halluces that could swivel outwardly while branch-walking and swivel inwardly while ground-walking.

    They
    allow for arboreal behaviors when necessary but don't
    harm the effectiveness of bipedality when the animal came down to the ground.
    *********************************************

    Erika doesn't argue the cause for these arboreal aspects, but only
    that their presence in chimpanzees and gorillas inhibits efficient bipedality. Anybody who has seen videos of gorillas and chimpanzees
    walking bipedally would agree they are much less efficient at it than
    are humans. Erika's point in paraphrase is that Lucy had a big butt, I cannot lie, and so walked more like humans do.

    Consider my earlier point about Homo erectus: thick heavy femur and skull occiput mechanically improved balance and pace while ground-walking orthogonally; this continued with neanderthals with pronounced occipital bun (bone + enlarged posteriorly
    cerebrum) and wide hips (Venus figurines?) and with Homo sapiens (software replaced mechanistic balancing, except in Khoisan and Andamaner females with very posterior buttocks (steatopygia), selected by long distance trekking.

    I wanted to go in depth on this video, but there is a massive noisy halloween celebration of trick or treating goblins and princesses here at the library. So enough.
    I hope you find time once the ghosts and goblins have gone.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to Daud Deden on Thu Nov 3 09:06:25 2022
    On Thursday, November 3, 2022 at 10:56:06 AM UTC-4, Daud Deden wrote:
    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote: >> Gutsick Gibbon is the Youtube handle of a biological anthropology PhD >> student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several >> papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several >> hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy.
    In another video, Top 3 Misconceptions about human evolution, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.

    Sahelanthropus has a flatter skull than modern chimps & humans. Chimps have a more prognathic muzzle, due to knucklewalking pronograde, derived from an ancestor with orthognathic muzzle. Chimp infant muzzles are more humanlike, more like sahelanthropus.
    At 6:20 Erika claims Miocene apes didn't knucklewalk (since their hands were more like humans than chimps), then she claims they were "pronograde palmigrade like most monkeys do today", that is false, they occasionally ground walked bipedally slowly on
    the forest floor, no quadrupedalism (all limbs in compression, which is selected for in open spaces to evade fast quadrupedal predators). https://youtu.be/g4FTbZLkpzU?t=388 Rather, they were slow brachiators, tightly grasping branches above rather than
    swiftly hooking them like modern hylobatids, so they had large strong thumbs and not very long fingers, unlike monkeys and extant apes. At 6:50, she says chimp hands are more 'evolved' than humans, that should be 'derived' (away from primitive). At 9:12
    she again talks about the LCA H\P as a monkey-like quadruped via Peter Andrew. That's not even possible. I don't know why she is pushing this fake paradigm.

    At 3:40 she talks about different modes of arboreal locomotion...she mentions "generalized miocene ape" & similar to "palmigrade pronograde arboreal quadrupeds of the miocene'.
    To me, the European miocene apes were arboreal slow bimanual brachiating & slow upright bipedal walking on horizontal tree branches.
    Is she referring to African miocene apes being pronograde palmigrade? Erika says this:
    *********************************
    Obviously australopithecus afarensis didn't evolve from a chimp but
    from sort of generalized Miocene ape. But that being said, the
    morphology of modern chimpanzees is at least similar to some of our palmigrade pronograde arboreal quadrupeds of the Miocene. *********************************

    So yes, Erika is saying at least some African Miocene apes were
    palmigrade aka foot parallel to the ground pronograde aka spine
    parallel to the ground, similar to modern chimpanzees.
    Chimps aren't palmigrade, no extant ape is, all monkeys are obligatory palmigrade. Humans are palmigrade only during infancy while knee-crawling and bear-walking (I'd guess only within a dome shelter). Humans and chimps hold tools in hands, but that's
    different from palmigrady.
    I don't know enough about Miocene apes to say if European and African
    apes were different. My understanding is climate change caused
    European Miocene apes to go extinct before Australopiths evolved in Africa, which suggests to me the two environments were different
    enough to support the differences you describe.
    I opine that European Miocene apes expanded from the Black Sea region after the MSC, some of their descendants included australopiths, Homo etc. entering Africa in waves.
    At 7:20, she apparently claims that chimp and gorilla arboreal traits interfere with their terrestrial locomotion "act to negate bipedalism" No, sleeping in bowl nests did that, selecting for short legs & backs.
    https://youtu.be/jo2ZLnucuHY?t=451
    Erika says this:
    ***********************************************
    Either way, the aspects that allow for arboriality found in australopithecus afarensis are not the same types as the ones that we
    find in chimpanzees and gorillas. In the latter two species, the
    arboreal aspects
    I guess 'aspect' could include arboreal bowl nesting, I thought she meant arboreal locomotion only.
    act to negate efficient bipedality,
    Not arboreal hylobatids. Bowl sleeping in great apes shrank their leg, achilles & back length.
    whereas in
    australopithecus afarensis they're sort of removed from it.
    The key is whether australopiths & kin had halluces that could swivel outwardly while branch-walking and swivel inwardly while ground-walking.
    They
    allow for arboreal behaviors when necessary but don't
    harm the effectiveness of bipedality when the animal came down to the ground.
    *********************************************

    Erika doesn't argue the cause for these arboreal aspects, but only
    that their presence in chimpanzees and gorillas inhibits efficient bipedality. Anybody who has seen videos of gorillas and chimpanzees walking bipedally would agree they are much less efficient at it than
    are humans. Erika's point in paraphrase is that Lucy had a big butt, I cannot lie, and so walked more like humans do.
    Consider my earlier point about Homo erectus: thick heavy femur and skull occiput mechanically improved balance and pace while ground-walking orthogonally; this continued with neanderthals with pronounced occipital bun (bone + enlarged posteriorly
    cerebrum) and wide hips (Venus figurines?) and with Homo sapiens (software replaced mechanistic balancing, except in Khoisan and Andamaner females with very posterior buttocks (steatopygia), selected by long distance trekking.
    I wanted to go in depth on this video, but there is a massive noisy halloween celebration of trick or treating goblins and princesses here at the library. So enough.
    I hope you find time once the ghosts and goblins have gone.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to Daud Deden on Thu Nov 3 09:54:57 2022
    On Thursday, November 3, 2022 at 12:06:26 PM UTC-4, Daud Deden wrote:
    On Thursday, November 3, 2022 at 10:56:06 AM UTC-4, Daud Deden wrote:
    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD >> student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in >> central-african Chad, and also because it may be the oldest bipedal >> hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism. >> She discusses several hypotheses, and presents compelling arguments >> for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy.
    In another video, Top 3 Misconceptions about human evolution, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus has a flatter skull than modern chimps & humans. Chimps have a more prognathic muzzle, due to knucklewalking pronograde, derived from an ancestor with orthognathic muzzle. Chimp infant muzzles are more humanlike, more like sahelanthropus.
    At 6:20 Erika claims Miocene apes didn't knucklewalk (since their hands were more like humans than chimps), then she claims they were "pronograde palmigrade like most monkeys do today", that is false, they occasionally ground walked bipedally slowly on
    the forest floor, no quadrupedalism (all limbs in compression, which is selected for in open spaces to evade fast quadrupedal predators). https://youtu.be/g4FTbZLkpzU?t=388 Rather, they were slow brachiators, tightly grasping branches above rather than
    swiftly hooking them like modern hylobatids, so they had large strong thumbs and not very long fingers, unlike monkeys and extant apes. At 6:50, she says chimp hands are more 'evolved' than humans, that should be 'derived' (away from primitive). At 9:12
    she again talks about the LCA H\P as a monkey-like quadruped via Peter Andrew. That's not even possible. I don't know why she is pushing this fake paradigm.
    At 3:40 she talks about different modes of arboreal locomotion...she mentions "generalized miocene ape" & similar to "palmigrade pronograde arboreal quadrupeds of the miocene'.
    To me, the European miocene apes were arboreal slow bimanual brachiating & slow upright bipedal walking on horizontal tree branches.
    Is she referring to African miocene apes being pronograde palmigrade? Erika says this:
    *********************************
    Obviously australopithecus afarensis didn't evolve from a chimp but
    from sort of generalized Miocene ape. But that being said, the morphology of modern chimpanzees is at least similar to some of our palmigrade pronograde arboreal quadrupeds of the Miocene. *********************************

    So yes, Erika is saying at least some African Miocene apes were palmigrade aka foot parallel to the ground pronograde aka spine
    parallel to the ground, similar to modern chimpanzees.
    Chimps aren't palmigrade, no extant ape is, all monkeys are obligatory palmigrade. Humans are palmigrade only during infancy while knee-crawling and bear-walking (I'd guess only within a dome shelter). Humans and chimps hold tools in hands, but that'
    s different from palmigrady.
    I don't know enough about Miocene apes to say if European and African apes were different. My understanding is climate change caused
    European Miocene apes to go extinct before Australopiths evolved in Africa, which suggests to me the two environments were different
    enough to support the differences you describe.
    I opine that European Miocene apes expanded from the Black Sea region after the MSC, some of their descendants included australopiths, Homo etc. entering Africa in waves.
    At 7:20, she apparently claims that chimp and gorilla arboreal traits interfere with their terrestrial locomotion "act to negate bipedalism" No, sleeping in bowl nests did that, selecting for short legs & backs.
    https://youtu.be/jo2ZLnucuHY?t=451
    Erika says this:
    ***********************************************
    Either way, the aspects that allow for arboriality found in australopithecus afarensis are not the same types as the ones that we find in chimpanzees and gorillas. In the latter two species, the arboreal aspects
    I guess 'aspect' could include arboreal bowl nesting, I thought she meant arboreal locomotion only.
    act to negate efficient bipedality,
    Not arboreal hylobatids. Bowl sleeping in great apes shrank their leg, achilles & back length.
    whereas in
    australopithecus afarensis they're sort of removed from it.
    The key is whether australopiths & kin had halluces that could swivel outwardly while branch-walking and swivel inwardly while ground-walking.
    They
    allow for arboreal behaviors when necessary but don't
    harm the effectiveness of bipedality when the animal came down to the ground.
    *********************************************

    Erika doesn't argue the cause for these arboreal aspects, but only
    that their presence in chimpanzees and gorillas inhibits efficient bipedality. Anybody who has seen videos of gorillas and chimpanzees walking bipedally would agree they are much less efficient at it than are humans. Erika's point in paraphrase is that Lucy had a big butt, I cannot lie, and so walked more like humans do.
    Consider my earlier point about Homo erectus: thick heavy femur and skull occiput mechanically improved balance and pace while ground-walking orthogonally; this continued with neanderthals with pronounced occipital bun (bone + enlarged posteriorly
    cerebrum) and wide hips (Venus figurines?) and with Homo sapiens (software replaced mechanistic balancing, except in Khoisan and Andamaner females with very posterior buttocks (steatopygia), selected by long distance trekking.
    I wanted to go in depth on this video, but there is a massive noisy halloween celebration of trick or treating goblins and princesses here at the library. So enough.
    I hope you find time once the ghosts and goblins have gone.

    I note that Wikipedia's article on brachiation is quite useful, but contains a blatant stupid falsehood. https://en.wikipedia.org/wiki/Brachiation

    'Currently, researchers classify gibbons and siamangs as the only true brachiators and classify the great apes as modified brachiators. Some traits that allow primates to brachiate include a short spine (particularity the lumbar spine)' [DD: 'primates'
    should be 'hominoids', 'particularity' is not a word, gibbons have a *long* spine, and are the only (fast) brachiators.
    Never trust Wikipedia to get it right.]

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to daud.deden@gmail.com on Thu Nov 3 18:28:59 2022
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden
    <daud.deden@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote: >> >> Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several >> >> papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several >> >> hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.


    Sahelanthropus tchadensis is neither Miocene nor European, but is a
    Pliocene central African species.


    At 3:40 she talks about different modes of arboreal locomotion...she mentions "generalized miocene ape" & similar to "palmigrade pronograde arboreal quadrupeds of the miocene'.
    To me, the European miocene apes were arboreal slow bimanual brachiating & slow upright bipedal walking on horizontal tree branches.
    Is she referring to African miocene apes being pronograde palmigrade?
    Erika says this:
    *********************************
    Obviously australopithecus afarensis didn't evolve from a chimp but
    from sort of generalized Miocene ape. But that being said, the
    morphology of modern chimpanzees is at least similar to some of our
    palmigrade pronograde arboreal quadrupeds of the Miocene.
    *********************************

    So yes, Erika is saying at least some African Miocene apes were
    palmigrade aka foot parallel to the ground pronograde aka spine
    parallel to the ground, similar to modern chimpanzees.

    Chimps aren't palmigrade, no extant ape is, all monkeys are obligatory palmigrade. Humans are palmigrade only during infancy while knee-crawling and bear-walking (I'd guess only within a dome shelter). Humans and chimps hold tools in hands, but that's
    different from palmigrady.


    You seem to have mixed palmigrade with pronograde.


    I don't know enough about Miocene apes to say if European and African
    apes were different. My understanding is climate change caused
    European Miocene apes to go extinct before Australopiths evolved in
    Africa, which suggests to me the two environments were different
    enough to support the differences you describe.

    I opine that European Miocene apes expanded from the Black Sea region after the MSC, some of their descendants included australopiths, Homo etc. entering Africa in waves.

    At 7:20, she apparently claims that chimp and gorilla arboreal traits interfere with their terrestrial locomotion "act to negate bipedalism" No, sleeping in bowl nests did that, selecting for short legs & backs.
    https://youtu.be/jo2ZLnucuHY?t=451
    Erika says this:
    *********************************************
    Either way, the aspects that allow for arboriality found in
    australopithecus afarensis are not the same types as the ones that we
    find in chimpanzees and gorillas. In the latter two species, the
    arboreal aspects

    I guess 'aspect' could include arboreal bowl nesting, I thought she meant arboreal locomotion only.

    act to negate efficient bipedality,

    Not arboreal hylobatids. Bowl sleeping in great apes shrank their leg, achilles & back length.


    My understanding is, when Erika refers to bipedality without
    qualifiers, she means terrestrial bipedality.


    whereas in
    australopithecus afarensis they're sort of removed from it.

    The key is whether australopiths & kin had halluces that could swivel outwardly while branch-walking and swivel inwardly while ground-walking.


    Erika persuasively argues that an outward hallux would help to
    stabilize a not-fully-developed terrestrial bipedal stance.


    They
    allow for arboreal behaviors when necessary but don't
    harm the effectiveness of bipedality when the animal came down to the
    ground.
    *********************************************

    Erika doesn't argue the cause for these arboreal aspects, but only
    that their presence in chimpanzees and gorillas inhibits efficient
    bipedality. Anybody who has seen videos of gorillas and chimpanzees
    walking bipedally would agree they are much less efficient at it than
    are humans. Erika's point in paraphrase is that Lucy had a big butt, I
    cannot lie, and so walked more like humans do.

    Consider my earlier point about Homo erectus: thick heavy femur and skull occiput mechanically improved balance and pace while ground-walking orthogonally; this continued with neanderthals with pronounced occipital bun (bone + enlarged posteriorly
    cerebrum) and wide hips (Venus figurines?) and with Homo sapiens (software replaced mechanistic balancing, except in Khoisan and Andamaner females with very posterior buttocks (steatopygia), selected by long distance trekking.

    I wanted to go in depth on this video, but there is a massive noisy halloween celebration of trick or treating goblins and princesses here at the library. So enough.
    I hope you find time once the ghosts and goblins have gone.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to Daud Deden on Thu Nov 3 15:21:48 2022
    On Thursday, November 3, 2022 at 12:54:58 PM UTC-4, Daud Deden wrote:
    On Thursday, November 3, 2022 at 12:06:26 PM UTC-4, Daud Deden wrote:
    On Thursday, November 3, 2022 at 10:56:06 AM UTC-4, Daud Deden wrote:
    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the >> latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal >> hominin fossil found to date. However, there appears to be strong >> disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments >> for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I cited, and refers to them, and so complete a logical trilogy.
    In another video, Top 3 Misconceptions about human evolution, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus has a flatter skull than modern chimps & humans. Chimps have a more prognathic muzzle, due to knucklewalking pronograde, derived from an ancestor with orthognathic muzzle. Chimp infant muzzles are more humanlike, more like
    sahelanthropus. At 6:20 Erika claims Miocene apes didn't knucklewalk (since their hands were more like humans than chimps), then she claims they were "pronograde palmigrade like most monkeys do today", that is false, they occasionally ground walked
    bipedally slowly on the forest floor, no quadrupedalism (all limbs in compression, which is selected for in open spaces to evade fast quadrupedal predators). https://youtu.be/g4FTbZLkpzU?t=388 Rather, they were slow brachiators, tightly grasping branches
    above rather than swiftly hooking them like modern hylobatids, so they had large strong thumbs and not very long fingers, unlike monkeys and extant apes. At 6:50, she says chimp hands are more 'evolved' than humans, that should be 'derived' (away from
    primitive). At 9:12 she again talks about the LCA H\P as a monkey-like quadruped via Peter Andrew. That's not even possible. I don't know why she is pushing this fake paradigm.
    At 3:40 she talks about different modes of arboreal locomotion...she mentions "generalized miocene ape" & similar to "palmigrade pronograde arboreal quadrupeds of the miocene'.
    To me, the European miocene apes were arboreal slow bimanual brachiating & slow upright bipedal walking on horizontal tree branches.
    Is she referring to African miocene apes being pronograde palmigrade? Erika says this:
    *********************************
    Obviously australopithecus afarensis didn't evolve from a chimp but from sort of generalized Miocene ape. But that being said, the morphology of modern chimpanzees is at least similar to some of our palmigrade pronograde arboreal quadrupeds of the Miocene. *********************************

    So yes, Erika is saying at least some African Miocene apes were palmigrade aka foot parallel to the ground pronograde aka spine parallel to the ground, similar to modern chimpanzees.
    Chimps aren't palmigrade, no extant ape is, all monkeys are obligatory palmigrade. Humans are palmigrade only during infancy while knee-crawling and bear-walking (I'd guess only within a dome shelter). Humans and chimps hold tools in hands, but
    that's different from palmigrady.
    I don't know enough about Miocene apes to say if European and African apes were different. My understanding is climate change caused European Miocene apes to go extinct before Australopiths evolved in Africa, which suggests to me the two environments were different enough to support the differences you describe.
    I opine that European Miocene apes expanded from the Black Sea region after the MSC, some of their descendants included australopiths, Homo etc. entering Africa in waves.
    At 7:20, she apparently claims that chimp and gorilla arboreal traits interfere with their terrestrial locomotion "act to negate bipedalism" No, sleeping in bowl nests did that, selecting for short legs & backs.
    https://youtu.be/jo2ZLnucuHY?t=451
    Erika says this:
    ***********************************************
    Either way, the aspects that allow for arboriality found in australopithecus afarensis are not the same types as the ones that we find in chimpanzees and gorillas. In the latter two species, the arboreal aspects
    I guess 'aspect' could include arboreal bowl nesting, I thought she meant arboreal locomotion only.
    act to negate efficient bipedality,
    Not arboreal hylobatids. Bowl sleeping in great apes shrank their leg, achilles & back length.
    whereas in
    australopithecus afarensis they're sort of removed from it.
    The key is whether australopiths & kin had halluces that could swivel outwardly while branch-walking and swivel inwardly while ground-walking.
    They
    allow for arboreal behaviors when necessary but don't
    harm the effectiveness of bipedality when the animal came down to the ground.
    *********************************************

    Erika doesn't argue the cause for these arboreal aspects, but only that their presence in chimpanzees and gorillas inhibits efficient bipedality. Anybody who has seen videos of gorillas and chimpanzees walking bipedally would agree they are much less efficient at it than are humans. Erika's point in paraphrase is that Lucy had a big butt, I cannot lie, and so walked more like humans do.
    Consider my earlier point about Homo erectus: thick heavy femur and skull occiput mechanically improved balance and pace while ground-walking orthogonally; this continued with neanderthals with pronounced occipital bun (bone + enlarged posteriorly
    cerebrum) and wide hips (Venus figurines?) and with Homo sapiens (software replaced mechanistic balancing, except in Khoisan and Andamaner females with very posterior buttocks (steatopygia), selected by long distance trekking.
    I wanted to go in depth on this video, but there is a massive noisy halloween celebration of trick or treating goblins and princesses here at the library. So enough.
    I hope you find time once the ghosts and goblins have gone.
    I note that Wikipedia's article on brachiation is quite useful, but contains a blatant stupid falsehood. https://en.wikipedia.org/wiki/Brachiation

    'Currently, researchers classify gibbons and siamangs as the only true brachiators and classify the great apes as modified brachiators. Some traits that allow primates to brachiate include a short spine (particularity the lumbar spine)' [DD: 'primates'
    should be 'hominoids', 'particularity' is not a word, gibbons have a *long* spine, and are the only (fast) brachiators.
    Never trust Wikipedia to get it right.]

    Side note:
    Qpedal palmigrade patas monkey top speed 35mph
    Qpedal kwalk chimp top speed 25mph
    Bpedal Hs Usain Bolt top speed 28mph
    Bimanual Hylobatid brachiation top speed 35mph

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Thu Nov 3 20:32:40 2022
    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote: >> On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD >> >> student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several >> >> papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in >> >> central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several >> >> hypotheses about *why* our ancestors shifted to obligate bipedalism. >> >> She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a
    Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.

    At 3:40 she talks about different modes of arboreal locomotion...she mentions "generalized miocene ape" & similar to "palmigrade pronograde arboreal quadrupeds of the miocene'.
    To me, the European miocene apes were arboreal slow bimanual brachiating & slow upright bipedal walking on horizontal tree branches.
    Is she referring to African miocene apes being pronograde palmigrade?
    Erika says this:
    *********************************
    Obviously australopithecus afarensis didn't evolve from a chimp but
    from sort of generalized Miocene ape. But that being said, the
    morphology of modern chimpanzees is at least similar to some of our
    palmigrade pronograde arboreal quadrupeds of the Miocene.
    *********************************

    So yes, Erika is saying at least some African Miocene apes were
    palmigrade aka foot parallel to the ground pronograde aka spine
    parallel to the ground, similar to modern chimpanzees.

    Chimps aren't palmigrade, no extant ape is, all monkeys are obligatory palmigrade. Humans are palmigrade only during infancy while knee-crawling and bear-walking (I'd guess only within a dome shelter). Humans and chimps hold tools in hands, but that's
    different from palmigrady.
    You seem to have mixed palmigrade with pronograde.

    Please cite specifically where I seem to have done that.

    I don't know enough about Miocene apes to say if European and African
    apes were different. My understanding is climate change caused
    European Miocene apes to go extinct before Australopiths evolved in
    Africa, which suggests to me the two environments were different
    enough to support the differences you describe.

    I opine that European Miocene apes expanded from the Black Sea region after the MSC, some of their descendants included australopiths, Homo etc. entering Africa in waves.

    At 7:20, she apparently claims that chimp and gorilla arboreal traits interfere with their terrestrial locomotion "act to negate bipedalism" No, sleeping in bowl nests did that, selecting for short legs & backs.
    https://youtu.be/jo2ZLnucuHY?t=451
    Erika says this:
    *********************************************
    Either way, the aspects that allow for arboriality found in
    australopithecus afarensis are not the same types as the ones that we
    find in chimpanzees and gorillas. In the latter two species, the
    arboreal aspects

    I guess 'aspect' could include arboreal bowl nesting, I thought she meant arboreal locomotion only.

    act to negate efficient bipedality,

    Not arboreal hylobatids. Bowl sleeping in great apes shrank their leg, achilles & back length.
    My understanding is, when Erika refers to bipedality without
    qualifiers, she means terrestrial bipedality.
    whereas in
    australopithecus afarensis they're sort of removed from it.

    The key is whether australopiths & kin had halluces that could swivel outwardly while branch-walking and swivel inwardly while ground-walking.
    Erika persuasively argues that an outward hallux would help to
    stabilize a not-fully-developed terrestrial bipedal stance.

    I presume that an "outward hallux" is a divergent hallux. That may differ from one that can swivel in or out per need. One that permanently stays divergent is a walking hazard, constantly snagging on vegetation, and would likely be selected against in a
    biped. Our toes have shortened, halluces converged, while our soles have lengthened providing postural stability.

    They
    allow for arboreal behaviors when necessary but don't
    harm the effectiveness of bipedality when the animal came down to the
    ground.
    *********************************************

    Erika doesn't argue the cause for these arboreal aspects, but only
    that their presence in chimpanzees and gorillas inhibits efficient
    bipedality. Anybody who has seen videos of gorillas and chimpanzees
    walking bipedally would agree they are much less efficient at it than
    are humans. Erika's point in paraphrase is that Lucy had a big butt, I
    cannot lie, and so walked more like humans do.

    Consider my earlier point about Homo erectus: thick heavy femur and skull occiput mechanically improved balance and pace while ground-walking orthogonally; this continued with neanderthals with pronounced occipital bun (bone + enlarged posteriorly
    cerebrum) and wide hips (Venus figurines?) and with Homo sapiens (software replaced mechanistic balancing, except in Khoisan and Andamaner females with very posterior buttocks (steatopygia), selected by long distance trekking.

    I wanted to go in depth on this video, but there is a massive noisy halloween celebration of trick or treating goblins and princesses here at the library. So enough.
    I hope you find time once the ghosts and goblins have gone.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to daud.deden@gmail.com on Fri Nov 4 02:21:55 2022
    On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden
    <daud.deden@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote: >> >> On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD >> >> >> student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in >> >> >> central-african Chad, and also because it may be the oldest bipedal >> >> >> hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism. >> >> >> She discusses several hypotheses, and presents compelling arguments >> >> >> for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a
    Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.


    My impression is there isn't enough evidence to show whether Pliocene
    African apes descended from Miocene European apes or Miocene African
    apes. Either way, there was enough time between the two eras to have
    evolved differences between either Miocene populations and Pliocene S. tchadensis.


    At 3:40 she talks about different modes of arboreal locomotion...she mentions "generalized miocene ape" & similar to "palmigrade pronograde arboreal quadrupeds of the miocene'.
    To me, the European miocene apes were arboreal slow bimanual brachiating & slow upright bipedal walking on horizontal tree branches.
    Is she referring to African miocene apes being pronograde palmigrade? >> >> Erika says this:
    *********************************
    Obviously australopithecus afarensis didn't evolve from a chimp but
    from sort of generalized Miocene ape. But that being said, the
    morphology of modern chimpanzees is at least similar to some of our
    palmigrade pronograde arboreal quadrupeds of the Miocene.
    *********************************

    So yes, Erika is saying at least some African Miocene apes were
    palmigrade aka foot parallel to the ground pronograde aka spine
    parallel to the ground, similar to modern chimpanzees.

    Chimps aren't palmigrade, no extant ape is, all monkeys are obligatory palmigrade. Humans are palmigrade only during infancy while knee-crawling and bear-walking (I'd guess only within a dome shelter). Humans and chimps hold tools in hands, but that'
    s different from palmigrady.
    You seem to have mixed palmigrade with pronograde.

    Please cite specifically where I seem to have done that.


    Just look at your sentence immediately above the one you challenge.
    Palmigrade is a scientific term to refer to locomotion with the whole
    foot on the ground, as with humans and apes when they walk bipedally.
    The feet of crawling infants are incidentally vertical to the ground
    aka not palmigrade, while their spine is nearly parallel to the ground
    aka pronograde.


    I don't know enough about Miocene apes to say if European and African
    apes were different. My understanding is climate change caused
    European Miocene apes to go extinct before Australopiths evolved in
    Africa, which suggests to me the two environments were different
    enough to support the differences you describe.

    I opine that European Miocene apes expanded from the Black Sea region after the MSC, some of their descendants included australopiths, Homo etc. entering Africa in waves.

    At 7:20, she apparently claims that chimp and gorilla arboreal traits interfere with their terrestrial locomotion "act to negate bipedalism" No, sleeping in bowl nests did that, selecting for short legs & backs.
    https://youtu.be/jo2ZLnucuHY?t=451
    Erika says this:
    *********************************************
    Either way, the aspects that allow for arboriality found in
    australopithecus afarensis are not the same types as the ones that we
    find in chimpanzees and gorillas. In the latter two species, the
    arboreal aspects

    I guess 'aspect' could include arboreal bowl nesting, I thought she meant arboreal locomotion only.

    act to negate efficient bipedality,

    Not arboreal hylobatids. Bowl sleeping in great apes shrank their leg, achilles & back length.
    My understanding is, when Erika refers to bipedality without
    qualifiers, she means terrestrial bipedality.
    whereas in
    australopithecus afarensis they're sort of removed from it.

    The key is whether australopiths & kin had halluces that could swivel outwardly while branch-walking and swivel inwardly while ground-walking.
    Erika persuasively argues that an outward hallux would help to
    stabilize a not-fully-developed terrestrial bipedal stance.

    I presume that an "outward hallux" is a divergent hallux. That may differ from one that can swivel in or out per need. One that permanently stays divergent is a walking hazard, constantly snagging on vegetation, and would likely be selected against in a
    biped. Our toes have shortened, halluces converged, while our soles have lengthened providing postural stability.


    My understanding is the primitive hallux was anatomically similar to
    the pollex, in that it was opposable under voluntary muscular control.
    So an "outward" (your word) hallux would not have been an impediment
    to walking on the ground. To the contrary, such a feature would be advantageous to organisms which moved both terrestrially and
    arboreally.

    As you say, modern humans have shortened parallel toes, a derived specialization for efficiently walking long distance on the ground.
    Personally, I can with difficulty move my big toes only a little in
    and out, like some crippled crab. However, I have a good friend who
    can move her big toes substantially and strongly, enough to painfully
    pinch other people's legs under the table while playing card games, to
    good strategic effect.


    They
    allow for arboreal behaviors when necessary but don't
    harm the effectiveness of bipedality when the animal came down to the
    ground.
    *********************************************

    Erika doesn't argue the cause for these arboreal aspects, but only
    that their presence in chimpanzees and gorillas inhibits efficient
    bipedality. Anybody who has seen videos of gorillas and chimpanzees
    walking bipedally would agree they are much less efficient at it than
    are humans. Erika's point in paraphrase is that Lucy had a big butt, I >> >> cannot lie, and so walked more like humans do.

    Consider my earlier point about Homo erectus: thick heavy femur and skull occiput mechanically improved balance and pace while ground-walking orthogonally; this continued with neanderthals with pronounced occipital bun (bone + enlarged posteriorly
    cerebrum) and wide hips (Venus figurines?) and with Homo sapiens (software replaced mechanistic balancing, except in Khoisan and Andamaner females with very posterior buttocks (steatopygia), selected by long distance trekking.

    I wanted to go in depth on this video, but there is a massive noisy halloween celebration of trick or treating goblins and princesses here at the library. So enough.
    I hope you find time once the ghosts and goblins have gone.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Fri Nov 4 11:01:30 2022
    On Friday, November 4, 2022 at 2:21:56 AM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote: >> On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the >> >> >> latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal >> >> >> hominin fossil found to date. However, there appears to be strong >> >> >> disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments >> >> >> for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a
    Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.
    My impression is there isn't enough evidence to show whether Pliocene African apes descended from Miocene European apes or Miocene African
    apes. Either way, there was enough time between the two eras to have
    evolved differences between either Miocene populations and Pliocene S. tchadensis.

    I agree. I didn't mean all 'Pliocene African apes', only Sahelanthropus, but might include some others.

    At 3:40 she talks about different modes of arboreal locomotion...she mentions "generalized miocene ape" & similar to "palmigrade pronograde arboreal quadrupeds of the miocene'.
    To me, the European miocene apes were arboreal slow bimanual brachiating & slow upright bipedal walking on horizontal tree branches.
    Is she referring to African miocene apes being pronograde palmigrade? >> >> Erika says this:
    *********************************
    Obviously australopithecus afarensis didn't evolve from a chimp but
    from sort of generalized Miocene ape. But that being said, the
    morphology of modern chimpanzees is at least similar to some of our
    palmigrade pronograde arboreal quadrupeds of the Miocene.
    *********************************

    So yes, Erika is saying at least some African Miocene apes were
    palmigrade aka foot parallel to the ground pronograde aka spine
    parallel to the ground, similar to modern chimpanzees.

    Chimps aren't palmigrade, no extant ape is, all monkeys are obligatory palmigrade. Humans are palmigrade only during infancy while knee-crawling and bear-walking (I'd guess only within a dome shelter). Humans and chimps hold tools in hands, but
    that's different from palmigrady.
    You seem to have mixed palmigrade with pronograde.

    Please cite specifically where I seem to have done that.

    Ok, my use of 'palmigrade' was in the palm-only sense, using plantigrade (sole) instead, since we normally refer to animals standing/walking on their feet, not their hands. I'll review things and adjust before responding, thanks for spotlighting the
    confusion, (my Bio background is more from botanical than zoological.). Some definitions are warranted.

    Palmigrade Etymology
    From Latin palma (“palm of the hand”) + gradi (“to walk”).

    palmigrade
    (zoology) Putting the whole foot upon the ground in walking, as some mammals do

    https://wikidiff.com/plantigrade/palmigrade

    https://en.m.wikipedia.org/wiki/Plantigrade
    Plantigrade mammal species include (but are not limited to): Some primates (including humans)
    Ailuridae: red pandas
    Ursidae: bears

    Just look at your sentence immediately above the one you challenge. Palmigrade is a scientific term to refer to locomotion with the whole
    foot on the ground, as with humans and apes when they walk bipedally.
    The feet of crawling infants are incidentally vertical to the ground
    aka not palmigrade, while their spine is nearly parallel to the ground
    aka pronograde.
    I don't know enough about Miocene apes to say if European and African >> >> apes were different. My understanding is climate change caused
    European Miocene apes to go extinct before Australopiths evolved in
    Africa, which suggests to me the two environments were different
    enough to support the differences you describe.

    I opine that European Miocene apes expanded from the Black Sea region after the MSC, some of their descendants included australopiths, Homo etc. entering Africa in waves.

    At 7:20, she apparently claims that chimp and gorilla arboreal traits interfere with their terrestrial locomotion "act to negate bipedalism" No, sleeping in bowl nests did that, selecting for short legs & backs.
    https://youtu.be/jo2ZLnucuHY?t=451
    Erika says this:
    *********************************************
    Either way, the aspects that allow for arboriality found in
    australopithecus afarensis are not the same types as the ones that we >> >> find in chimpanzees and gorillas. In the latter two species, the
    arboreal aspects

    I guess 'aspect' could include arboreal bowl nesting, I thought she meant arboreal locomotion only.

    act to negate efficient bipedality,

    Not arboreal hylobatids. Bowl sleeping in great apes shrank their leg, achilles & back length.
    My understanding is, when Erika refers to bipedality without
    qualifiers, she means terrestrial bipedality.
    whereas in
    australopithecus afarensis they're sort of removed from it.

    The key is whether australopiths & kin had halluces that could swivel outwardly while branch-walking and swivel inwardly while ground-walking.
    Erika persuasively argues that an outward hallux would help to
    stabilize a not-fully-developed terrestrial bipedal stance.

    I presume that an "outward hallux" is a divergent hallux. That may differ from one that can swivel in or out per need. One that permanently stays divergent is a walking hazard, constantly snagging on vegetation, and would likely be selected against in
    a biped. Our toes have shortened, halluces converged, while our soles have lengthened providing postural stability.
    My understanding is the primitive hallux was anatomically similar to
    the pollex, in that it was opposable under voluntary muscular control.
    So an "outward" (your word) hallux would not have been an impediment
    to walking on the ground. To the contrary, such a feature would be advantageous to organisms which moved both terrestrially and
    arboreally.

    As you say, modern humans have shortened parallel toes, a derived specialization for efficiently walking long distance on the ground. Personally, I can with difficulty move my big toes only a little in
    and out, like some crippled crab. However, I have a good friend who
    can move her big toes substantially and strongly, enough to painfully
    pinch other people's legs under the table while playing card games, to
    good strategic effect.
    :~}
    They
    allow for arboreal behaviors when necessary but don't
    harm the effectiveness of bipedality when the animal came down to the >> >> ground.
    *********************************************

    Erika doesn't argue the cause for these arboreal aspects, but only
    that their presence in chimpanzees and gorillas inhibits efficient
    bipedality. Anybody who has seen videos of gorillas and chimpanzees
    walking bipedally would agree they are much less efficient at it than >> >> are humans. Erika's point in paraphrase is that Lucy had a big butt, I >> >> cannot lie, and so walked more like humans do.

    Consider my earlier point about Homo erectus: thick heavy femur and skull occiput mechanically improved balance and pace while ground-walking orthogonally; this continued with neanderthals with pronounced occipital bun (bone + enlarged posteriorly
    cerebrum) and wide hips (Venus figurines?) and with Homo sapiens (software replaced mechanistic balancing, except in Khoisan and Andamaner females with very posterior buttocks (steatopygia), selected by long distance trekking.

    I wanted to go in depth on this video, but there is a massive noisy halloween celebration of trick or treating goblins and princesses here at the library. So enough.
    I hope you find time once the ghosts and goblins have gone.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to daud.deden@gmail.com on Sat Nov 5 02:25:10 2022
    On Fri, 4 Nov 2022 11:01:30 -0700 (PDT), Daud Deden
    <daud.deden@gmail.com> wrote:

    On Friday, November 4, 2022 at 2:21:56 AM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the >> >> >> >> latest developments relating to the origins of human bipedalism: >> >> >> >>
    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong >> >> >> >> disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a
    Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.
    My impression is there isn't enough evidence to show whether Pliocene
    African apes descended from Miocene European apes or Miocene African
    apes. Either way, there was enough time between the two eras to have
    evolved differences between either Miocene populations and Pliocene S.
    tchadensis.

    I agree. I didn't mean all 'Pliocene African apes', only Sahelanthropus, but might include some others.

    At 3:40 she talks about different modes of arboreal locomotion...she mentions "generalized miocene ape" & similar to "palmigrade pronograde arboreal quadrupeds of the miocene'.
    To me, the European miocene apes were arboreal slow bimanual brachiating & slow upright bipedal walking on horizontal tree branches.
    Is she referring to African miocene apes being pronograde palmigrade?
    Erika says this:
    *********************************
    Obviously australopithecus afarensis didn't evolve from a chimp but >> >> >> from sort of generalized Miocene ape. But that being said, the
    morphology of modern chimpanzees is at least similar to some of our >> >> >> palmigrade pronograde arboreal quadrupeds of the Miocene.
    *********************************

    So yes, Erika is saying at least some African Miocene apes were
    palmigrade aka foot parallel to the ground pronograde aka spine
    parallel to the ground, similar to modern chimpanzees.

    Chimps aren't palmigrade, no extant ape is, all monkeys are obligatory palmigrade. Humans are palmigrade only during infancy while knee-crawling and bear-walking (I'd guess only within a dome shelter). Humans and chimps hold tools in hands, but
    that's different from palmigrady.
    You seem to have mixed palmigrade with pronograde.

    Please cite specifically where I seem to have done that.

    Just look at your sentence immediately above the one you challenge.
    Palmigrade is a scientific term to refer to locomotion with the whole
    foot on the ground, as with humans and apes when they walk bipedally.
    The feet of crawling infants are incidentally vertical to the ground
    aka not palmigrade, while their spine is nearly parallel to the ground
    aka pronograde.

    Ok, my use of 'palmigrade' was in the palm-only sense, using plantigrade (sole) instead, since we normally refer to animals standing/walking on their feet, not their hands. I'll review things and adjust before responding, thanks for spotlighting the
    confusion, (my Bio background is more from botanical than zoological.). Some definitions are warranted.

    Palmigrade Etymology
    From Latin palma (“palm of the hand”) + gradi (“to walk”).

    palmigrade
    (zoology) Putting the whole foot upon the ground in walking, as some mammals do

    https://wikidiff.com/plantigrade/palmigrade

    https://en.m.wikipedia.org/wiki/Plantigrade
    Plantigrade mammal species include (but are not limited to): >Some primates (including humans)
    Ailuridae: red pandas
    Ursidae: bears


    Ok. I too am unfamiliar with the distinction between palmigrade and plantigrade. One source I found said "palmigrade" is an adjective and "plantigrade" is a noun, but that just adds to the confusion.

    Anatomically, the relevant distinction is how much of the foot rests
    on the ground when walking, either plantigrade, digitigrade or
    unguligrade.

    For primates, the importance of fingers as manipulating tools means
    they necessarily compromise the hand's anatomy for locomotion. For
    arboreal primates, the phalanges are curved to better grasp branches.
    For quadruped primates, the hands may be flat on the ground as with
    baboons. Facultative bipedal primates may use knuckle-walking as with chimpanzees.

    For obligate bipeds like genus homo, the hands aren't used for
    locomotion at all, and their anatomy is devoted to manipulation. My understanding is genus australopithecus are transitional between
    arboreal bipedal primates and terrestrial bipedal primates.


    I don't know enough about Miocene apes to say if European and African >> >> >> apes were different. My understanding is climate change caused
    European Miocene apes to go extinct before Australopiths evolved in >> >> >> Africa, which suggests to me the two environments were different
    enough to support the differences you describe.

    I opine that European Miocene apes expanded from the Black Sea region after the MSC, some of their descendants included australopiths, Homo etc. entering Africa in waves.

    At 7:20, she apparently claims that chimp and gorilla arboreal traits interfere with their terrestrial locomotion "act to negate bipedalism" No, sleeping in bowl nests did that, selecting for short legs & backs.
    https://youtu.be/jo2ZLnucuHY?t=451
    Erika says this:
    *********************************************
    Either way, the aspects that allow for arboriality found in
    australopithecus afarensis are not the same types as the ones that we >> >> >> find in chimpanzees and gorillas. In the latter two species, the
    arboreal aspects

    I guess 'aspect' could include arboreal bowl nesting, I thought she meant arboreal locomotion only.

    act to negate efficient bipedality,

    Not arboreal hylobatids. Bowl sleeping in great apes shrank their leg, achilles & back length.
    My understanding is, when Erika refers to bipedality without
    qualifiers, she means terrestrial bipedality.
    whereas in
    australopithecus afarensis they're sort of removed from it.

    The key is whether australopiths & kin had halluces that could swivel outwardly while branch-walking and swivel inwardly while ground-walking.
    Erika persuasively argues that an outward hallux would help to
    stabilize a not-fully-developed terrestrial bipedal stance.

    I presume that an "outward hallux" is a divergent hallux. That may differ from one that can swivel in or out per need. One that permanently stays divergent is a walking hazard, constantly snagging on vegetation, and would likely be selected against
    in a biped. Our toes have shortened, halluces converged, while our soles have lengthened providing postural stability.
    My understanding is the primitive hallux was anatomically similar to
    the pollex, in that it was opposable under voluntary muscular control.
    So an "outward" (your word) hallux would not have been an impediment
    to walking on the ground. To the contrary, such a feature would be
    advantageous to organisms which moved both terrestrially and
    arboreally.

    As you say, modern humans have shortened parallel toes, a derived
    specialization for efficiently walking long distance on the ground.
    Personally, I can with difficulty move my big toes only a little in
    and out, like some crippled crab. However, I have a good friend who
    can move her big toes substantially and strongly, enough to painfully
    pinch other people's legs under the table while playing card games, to
    good strategic effect.
    :~}
    They
    allow for arboreal behaviors when necessary but don't
    harm the effectiveness of bipedality when the animal came down to the >> >> >> ground.
    *********************************************

    Erika doesn't argue the cause for these arboreal aspects, but only
    that their presence in chimpanzees and gorillas inhibits efficient
    bipedality. Anybody who has seen videos of gorillas and chimpanzees >> >> >> walking bipedally would agree they are much less efficient at it than >> >> >> are humans. Erika's point in paraphrase is that Lucy had a big butt, I
    cannot lie, and so walked more like humans do.

    Consider my earlier point about Homo erectus: thick heavy femur and skull occiput mechanically improved balance and pace while ground-walking orthogonally; this continued with neanderthals with pronounced occipital bun (bone + enlarged posteriorly
    cerebrum) and wide hips (Venus figurines?) and with Homo sapiens (software replaced mechanistic balancing, except in Khoisan and Andamaner females with very posterior buttocks (steatopygia), selected by long distance trekking.

    I wanted to go in depth on this video, but there is a massive noisy halloween celebration of trick or treating goblins and princesses here at the library. So enough.
    I hope you find time once the ghosts and goblins have gone.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Sat Nov 5 20:05:10 2022
    On Saturday, November 5, 2022 at 2:25:13 AM UTC-4, 69jp...@gmail.com wrote:
    On Fri, 4 Nov 2022 11:01:30 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, November 4, 2022 at 2:21:56 AM UTC-4, 69jp...@gmail.com wrote: >> On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism: >> >> >> >>
    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a
    Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.
    My impression is there isn't enough evidence to show whether Pliocene
    African apes descended from Miocene European apes or Miocene African
    apes. Either way, there was enough time between the two eras to have
    evolved differences between either Miocene populations and Pliocene S.
    tchadensis.

    I agree. I didn't mean all 'Pliocene African apes', only Sahelanthropus, but might include some others.

    At 3:40 she talks about different modes of arboreal locomotion...she mentions "generalized miocene ape" & similar to "palmigrade pronograde arboreal quadrupeds of the miocene'.
    To me, the European miocene apes were arboreal slow bimanual brachiating & slow upright bipedal walking on horizontal tree branches.
    Is she referring to African miocene apes being pronograde palmigrade?
    Erika says this:
    *********************************
    Obviously australopithecus afarensis didn't evolve from a chimp but >> >> >> from sort of generalized Miocene ape. But that being said, the
    morphology of modern chimpanzees is at least similar to some of our >> >> >> palmigrade pronograde arboreal quadrupeds of the Miocene.
    *********************************

    So yes, Erika is saying at least some African Miocene apes were
    palmigrade aka foot parallel to the ground pronograde aka spine
    parallel to the ground, similar to modern chimpanzees.

    Chimps aren't palmigrade, no extant ape is, all monkeys are obligatory palmigrade. Humans are palmigrade only during infancy while knee-crawling and bear-walking (I'd guess only within a dome shelter). Humans and chimps hold tools in hands, but
    that's different from palmigrady.
    You seem to have mixed palmigrade with pronograde.

    Please cite specifically where I seem to have done that.

    Just look at your sentence immediately above the one you challenge.
    Palmigrade is a scientific term to refer to locomotion with the whole
    foot on the ground, as with humans and apes when they walk bipedally.
    The feet of crawling infants are incidentally vertical to the ground
    aka not palmigrade, while their spine is nearly parallel to the ground
    aka pronograde.

    Ok, my use of 'palmigrade' was in the palm-only sense, using plantigrade (sole) instead, since we normally refer to animals standing/walking on their feet, not their hands. I'll review things and adjust before responding, thanks for spotlighting the
    confusion, (my Bio background is more from botanical than zoological.). Some definitions are warranted.

    Palmigrade Etymology
    From Latin palma (“palm of the hand”) + gradi (“to walk”).

    palmigrade
    (zoology) Putting the whole foot upon the ground in walking, as some mammals do

    https://wikidiff.com/plantigrade/palmigrade

    https://en.m.wikipedia.org/wiki/Plantigrade
    Plantigrade mammal species include (but are not limited to):
    Some primates (including humans)
    Ailuridae: red pandas
    Ursidae: bears
    Ok. I too am unfamiliar with the distinction between palmigrade and plantigrade. One source I found said "palmigrade" is an adjective and "plantigrade" is a noun, but that just adds to the confusion.
    Yes, both can be noun or adjective as needed, -grade, -grady.
    Anatomically, the relevant distinction is how much of the foot rests
    on the ground when walking, either plantigrade, digitigrade or
    unguligrade.
    Yes. Knucklewalking fits in-between, plantigrade hind limbs & digitigrade (dorsal) forelimbs.
    For primates, the importance of fingers as manipulating tools means
    they necessarily compromise the hand's anatomy for locomotion. For
    arboreal primates, the phalanges are curved to better grasp branches.
    For quadruped primates, the hands may be flat on the ground as with
    baboons. Facultative bipedal primates may use knuckle-walking as with chimpanzees.
    Yes. Rainforest drills have shortish fingers, they walk on their fingertips not palms.
    For obligate bipeds like genus homo, the hands aren't used for
    locomotion at all, and their anatomy is devoted to manipulation. My understanding is genus australopithecus are transitional between
    arboreal bipedal primates and terrestrial bipedal primates.
    I liked this Sci Am article, especially near the end, section called Open Question.
    https://www.scientificamerican.com/article/fossils-upend-conventional-wisdom-about-evolution-of-human-bipedalism/

    I don't know enough about Miocene apes to say if European and African
    apes were different. My understanding is climate change caused
    European Miocene apes to go extinct before Australopiths evolved in >> >> >> Africa, which suggests to me the two environments were different
    enough to support the differences you describe.

    I opine that European Miocene apes expanded from the Black Sea region after the MSC, some of their descendants included australopiths, Homo etc. entering Africa in waves.

    At 7:20, she apparently claims that chimp and gorilla arboreal traits interfere with their terrestrial locomotion "act to negate bipedalism" No, sleeping in bowl nests did that, selecting for short legs & backs.
    https://youtu.be/jo2ZLnucuHY?t=451
    Erika says this:
    *********************************************
    Either way, the aspects that allow for arboriality found in
    australopithecus afarensis are not the same types as the ones that we
    find in chimpanzees and gorillas. In the latter two species, the
    arboreal aspects

    I guess 'aspect' could include arboreal bowl nesting, I thought she meant arboreal locomotion only.

    act to negate efficient bipedality,

    Not arboreal hylobatids. Bowl sleeping in great apes shrank their leg, achilles & back length.
    My understanding is, when Erika refers to bipedality without
    qualifiers, she means terrestrial bipedality.
    whereas in
    australopithecus afarensis they're sort of removed from it.

    The key is whether australopiths & kin had halluces that could swivel outwardly while branch-walking and swivel inwardly while ground-walking.
    Erika persuasively argues that an outward hallux would help to
    stabilize a not-fully-developed terrestrial bipedal stance.

    I presume that an "outward hallux" is a divergent hallux. That may differ from one that can swivel in or out per need. One that permanently stays divergent is a walking hazard, constantly snagging on vegetation, and would likely be selected against
    in a biped. Our toes have shortened, halluces converged, while our soles have lengthened providing postural stability.
    My understanding is the primitive hallux was anatomically similar to
    the pollex, in that it was opposable under voluntary muscular control.
    So an "outward" (your word) hallux would not have been an impediment
    to walking on the ground. To the contrary, such a feature would be
    advantageous to organisms which moved both terrestrially and
    arboreally.

    As you say, modern humans have shortened parallel toes, a derived
    specialization for efficiently walking long distance on the ground.
    Personally, I can with difficulty move my big toes only a little in
    and out, like some crippled crab. However, I have a good friend who
    can move her big toes substantially and strongly, enough to painfully
    pinch other people's legs under the table while playing card games, to
    good strategic effect.
    :~}
    They
    allow for arboreal behaviors when necessary but don't
    harm the effectiveness of bipedality when the animal came down to the
    ground.
    *********************************************

    Erika doesn't argue the cause for these arboreal aspects, but only >> >> >> that their presence in chimpanzees and gorillas inhibits efficient >> >> >> bipedality. Anybody who has seen videos of gorillas and chimpanzees >> >> >> walking bipedally would agree they are much less efficient at it than
    are humans. Erika's point in paraphrase is that Lucy had a big butt, I
    cannot lie, and so walked more like humans do.

    Consider my earlier point about Homo erectus: thick heavy femur and skull occiput mechanically improved balance and pace while ground-walking orthogonally; this continued with neanderthals with pronounced occipital bun (bone + enlarged
    posteriorly cerebrum) and wide hips (Venus figurines?) and with Homo sapiens (software replaced mechanistic balancing, except in Khoisan and Andamaner females with very posterior buttocks (steatopygia), selected by long distance trekking.

    I wanted to go in depth on this video, but there is a massive noisy halloween celebration of trick or treating goblins and princesses here at the library. So enough.
    I hope you find time once the ghosts and goblins have gone.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to All on Sun Nov 6 00:03:09 2022
    <Full snip for focus>
    As you say, modern humans have shortened parallel toes, a derived specialization for efficiently walking long distance on the ground. Personally, I can with difficulty move my big toes only a little in
    and out, like some crippled crab. However, I have a good friend who
    can move her big toes substantially and strongly, enough to painfully
    pinch other people's legs under the table while playing card games, to
    good strategic effect.

    Our comfy confining cushioned shoes can cripple... this video short shows Barefoot shoes can return them to health. https://youtube.com/shorts/EOxOrxggBMI?feature=share

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to daud.deden@gmail.com on Sun Nov 6 11:52:35 2022
    On Sun, 6 Nov 2022 00:03:09 -0700 (PDT), Daud Deden
    <daud.deden@gmail.com> wrote:


    <Full snip for focus>
    As you say, modern humans have shortened parallel toes, a derived
    specialization for efficiently walking long distance on the ground.
    Personally, I can with difficulty move my big toes only a little in
    and out, like some crippled crab. However, I have a good friend who
    can move her big toes substantially and strongly, enough to painfully
    pinch other people's legs under the table while playing card games, to
    good strategic effect.

    Our comfy confining cushioned shoes can cripple... this video short shows Barefoot shoes can return them to health. https://youtube.com/shorts/EOxOrxggBMI?feature=share


    Interesting you mention that. She grew up in Hawaii when going around
    shoeless was common.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to daud.deden@gmail.com on Sun Nov 6 11:50:17 2022
    On Sat, 5 Nov 2022 20:05:10 -0700 (PDT), Daud Deden
    <daud.deden@gmail.com> wrote:

    On Saturday, November 5, 2022 at 2:25:13 AM UTC-4, 69jp...@gmail.com wrote:
    On Fri, 4 Nov 2022 11:01:30 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, November 4, 2022 at 2:21:56 AM UTC-4, 69jp...@gmail.com wrote: >> >> On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY >> >> >> >> Thank you for citing the above video. It's prelude to the ones I >> >> >> >> cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a >> >> >> Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.
    My impression is there isn't enough evidence to show whether Pliocene
    African apes descended from Miocene European apes or Miocene African
    apes. Either way, there was enough time between the two eras to have
    evolved differences between either Miocene populations and Pliocene S. >> >> tchadensis.

    I agree. I didn't mean all 'Pliocene African apes', only Sahelanthropus, but might include some others.

    At 3:40 she talks about different modes of arboreal locomotion...she mentions "generalized miocene ape" & similar to "palmigrade pronograde arboreal quadrupeds of the miocene'.
    To me, the European miocene apes were arboreal slow bimanual brachiating & slow upright bipedal walking on horizontal tree branches.
    Is she referring to African miocene apes being pronograde palmigrade?
    Erika says this:
    *********************************
    Obviously australopithecus afarensis didn't evolve from a chimp but
    from sort of generalized Miocene ape. But that being said, the
    morphology of modern chimpanzees is at least similar to some of our
    palmigrade pronograde arboreal quadrupeds of the Miocene.
    *********************************

    So yes, Erika is saying at least some African Miocene apes were
    palmigrade aka foot parallel to the ground pronograde aka spine
    parallel to the ground, similar to modern chimpanzees.

    Chimps aren't palmigrade, no extant ape is, all monkeys are obligatory palmigrade. Humans are palmigrade only during infancy while knee-crawling and bear-walking (I'd guess only within a dome shelter). Humans and chimps hold tools in hands, but
    that's different from palmigrady.
    You seem to have mixed palmigrade with pronograde.

    Please cite specifically where I seem to have done that.

    Just look at your sentence immediately above the one you challenge.
    Palmigrade is a scientific term to refer to locomotion with the whole
    foot on the ground, as with humans and apes when they walk bipedally.
    The feet of crawling infants are incidentally vertical to the ground
    aka not palmigrade, while their spine is nearly parallel to the ground >> >> aka pronograde.

    Ok, my use of 'palmigrade' was in the palm-only sense, using plantigrade (sole) instead, since we normally refer to animals standing/walking on their feet, not their hands. I'll review things and adjust before responding, thanks for spotlighting the
    confusion, (my Bio background is more from botanical than zoological.). Some definitions are warranted.

    Palmigrade Etymology
    From Latin palma (“palm of the hand”) + gradi (“to walk”).

    palmigrade
    (zoology) Putting the whole foot upon the ground in walking, as some mammals do

    https://wikidiff.com/plantigrade/palmigrade

    https://en.m.wikipedia.org/wiki/Plantigrade
    Plantigrade mammal species include (but are not limited to):
    Some primates (including humans)
    Ailuridae: red pandas
    Ursidae: bears
    Ok. I too am unfamiliar with the distinction between palmigrade and
    plantigrade. One source I found said "palmigrade" is an adjective and
    "plantigrade" is a noun, but that just adds to the confusion.
    Yes, both can be noun or adjective as needed, -grade, -grady.
    Anatomically, the relevant distinction is how much of the foot rests
    on the ground when walking, either plantigrade, digitigrade or
    unguligrade.
    Yes. Knucklewalking fits in-between, plantigrade hind limbs & digitigrade (dorsal) forelimbs.


    My understanding is those terms apply equally to both forelimbs and
    hindlimbs.


    For primates, the importance of fingers as manipulating tools means
    they necessarily compromise the hand's anatomy for locomotion. For
    arboreal primates, the phalanges are curved to better grasp branches.
    For quadruped primates, the hands may be flat on the ground as with
    baboons. Facultative bipedal primates may use knuckle-walking as with
    chimpanzees.
    Yes. Rainforest drills have shortish fingers, they walk on their fingertips not palms.
    For obligate bipeds like genus homo, the hands aren't used for
    locomotion at all, and their anatomy is devoted to manipulation. My
    understanding is genus australopithecus are transitional between
    arboreal bipedal primates and terrestrial bipedal primates.
    I liked this Sci Am article, especially near the end, section called Open Question.
    https://www.scientificamerican.com/article/fossils-upend-conventional-wisdom-about-evolution-of-human-bipedalism/


    Thanks for the link. Are you familiar with a book called "Contested
    Bones"? Erika does a multi-part and extremely detailed critique of
    it.


    I don't know enough about Miocene apes to say if European and African
    apes were different. My understanding is climate change caused
    European Miocene apes to go extinct before Australopiths evolved in
    Africa, which suggests to me the two environments were different >> >> >> >> enough to support the differences you describe.

    I opine that European Miocene apes expanded from the Black Sea region after the MSC, some of their descendants included australopiths, Homo etc. entering Africa in waves.

    At 7:20, she apparently claims that chimp and gorilla arboreal traits interfere with their terrestrial locomotion "act to negate bipedalism" No, sleeping in bowl nests did that, selecting for short legs & backs.
    https://youtu.be/jo2ZLnucuHY?t=451
    Erika says this:
    *********************************************
    Either way, the aspects that allow for arboriality found in
    australopithecus afarensis are not the same types as the ones that we
    find in chimpanzees and gorillas. In the latter two species, the >> >> >> >> arboreal aspects

    I guess 'aspect' could include arboreal bowl nesting, I thought she meant arboreal locomotion only.

    act to negate efficient bipedality,

    Not arboreal hylobatids. Bowl sleeping in great apes shrank their leg, achilles & back length.
    My understanding is, when Erika refers to bipedality without
    qualifiers, she means terrestrial bipedality.
    whereas in
    australopithecus afarensis they're sort of removed from it.

    The key is whether australopiths & kin had halluces that could swivel outwardly while branch-walking and swivel inwardly while ground-walking.
    Erika persuasively argues that an outward hallux would help to
    stabilize a not-fully-developed terrestrial bipedal stance.

    I presume that an "outward hallux" is a divergent hallux. That may differ from one that can swivel in or out per need. One that permanently stays divergent is a walking hazard, constantly snagging on vegetation, and would likely be selected
    against in a biped. Our toes have shortened, halluces converged, while our soles have lengthened providing postural stability.
    My understanding is the primitive hallux was anatomically similar to
    the pollex, in that it was opposable under voluntary muscular control. >> >> So an "outward" (your word) hallux would not have been an impediment
    to walking on the ground. To the contrary, such a feature would be
    advantageous to organisms which moved both terrestrially and
    arboreally.

    As you say, modern humans have shortened parallel toes, a derived
    specialization for efficiently walking long distance on the ground.
    Personally, I can with difficulty move my big toes only a little in
    and out, like some crippled crab. However, I have a good friend who
    can move her big toes substantially and strongly, enough to painfully
    pinch other people's legs under the table while playing card games, to >> >> good strategic effect.
    :~}
    They
    allow for arboreal behaviors when necessary but don't
    harm the effectiveness of bipedality when the animal came down to the
    ground.
    *********************************************

    Erika doesn't argue the cause for these arboreal aspects, but only >> >> >> >> that their presence in chimpanzees and gorillas inhibits efficient >> >> >> >> bipedality. Anybody who has seen videos of gorillas and chimpanzees
    walking bipedally would agree they are much less efficient at it than
    are humans. Erika's point in paraphrase is that Lucy had a big butt, I
    cannot lie, and so walked more like humans do.

    Consider my earlier point about Homo erectus: thick heavy femur and skull occiput mechanically improved balance and pace while ground-walking orthogonally; this continued with neanderthals with pronounced occipital bun (bone + enlarged
    posteriorly cerebrum) and wide hips (Venus figurines?) and with Homo sapiens (software replaced mechanistic balancing, except in Khoisan and Andamaner females with very posterior buttocks (steatopygia), selected by long distance trekking.

    I wanted to go in depth on this video, but there is a massive noisy halloween celebration of trick or treating goblins and princesses here at the library. So enough.
    I hope you find time once the ghosts and goblins have gone.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Mon Nov 7 14:03:13 2022
    On Sunday, November 6, 2022 at 11:52:37 AM UTC-5, 69jp...@gmail.com wrote:
    On Sun, 6 Nov 2022 00:03:09 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:


    <Full snip for focus>
    As you say, modern humans have shortened parallel toes, a derived
    specialization for efficiently walking long distance on the ground.
    Personally, I can with difficulty move my big toes only a little in
    and out, like some crippled crab. However, I have a good friend who
    can move her big toes substantially and strongly, enough to painfully
    pinch other people's legs under the table while playing card games, to
    good strategic effect.

    Our comfy confining cushioned shoes can cripple... this video short shows Barefoot shoes can return them to health. https://youtube.com/shorts/EOxOrxggBMI?feature=share
    Interesting you mention that. She grew up in Hawaii when going around shoeless was common.
    I'm from Minnesota, shod always but in bed or bath.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Mon Nov 7 13:57:52 2022
    On Sunday, November 6, 2022 at 11:50:21 AM UTC-5, 69jp...@gmail.com wrote:
    On Sat, 5 Nov 2022 20:05:10 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Saturday, November 5, 2022 at 2:25:13 AM UTC-4, 69jp...@gmail.com wrote: >> On Fri, 4 Nov 2022 11:01:30 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, November 4, 2022 at 2:21:56 AM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is >> >> >> >> >> remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY >> >> >> >> Thank you for citing the above video. It's prelude to the ones I >> >> >> >> cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a >> >> >> Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.
    My impression is there isn't enough evidence to show whether Pliocene >> >> African apes descended from Miocene European apes or Miocene African >> >> apes. Either way, there was enough time between the two eras to have >> >> evolved differences between either Miocene populations and Pliocene S. >> >> tchadensis.

    I agree. I didn't mean all 'Pliocene African apes', only Sahelanthropus, but might include some others.

    At 3:40 she talks about different modes of arboreal locomotion...she mentions "generalized miocene ape" & similar to "palmigrade pronograde arboreal quadrupeds of the miocene'.
    To me, the European miocene apes were arboreal slow bimanual brachiating & slow upright bipedal walking on horizontal tree branches.
    Is she referring to African miocene apes being pronograde palmigrade?
    Erika says this:
    *********************************
    Obviously australopithecus afarensis didn't evolve from a chimp but
    from sort of generalized Miocene ape. But that being said, the >> >> >> >> morphology of modern chimpanzees is at least similar to some of our
    palmigrade pronograde arboreal quadrupeds of the Miocene.
    *********************************

    So yes, Erika is saying at least some African Miocene apes were >> >> >> >> palmigrade aka foot parallel to the ground pronograde aka spine >> >> >> >> parallel to the ground, similar to modern chimpanzees.

    Chimps aren't palmigrade, no extant ape is, all monkeys are obligatory palmigrade. Humans are palmigrade only during infancy while knee-crawling and bear-walking (I'd guess only within a dome shelter). Humans and chimps hold tools in hands,
    but that's different from palmigrady.
    You seem to have mixed palmigrade with pronograde.

    Please cite specifically where I seem to have done that.

    Just look at your sentence immediately above the one you challenge.
    Palmigrade is a scientific term to refer to locomotion with the whole >> >> foot on the ground, as with humans and apes when they walk bipedally. >> >> The feet of crawling infants are incidentally vertical to the ground >> >> aka not palmigrade, while their spine is nearly parallel to the ground >> >> aka pronograde.

    Ok, my use of 'palmigrade' was in the palm-only sense, using plantigrade (sole) instead, since we normally refer to animals standing/walking on their feet, not their hands. I'll review things and adjust before responding, thanks for spotlighting
    the confusion, (my Bio background is more from botanical than zoological.). Some definitions are warranted.

    Palmigrade Etymology
    From Latin palma (“palm of the hand”) + gradi (“to walk”).

    palmigrade
    (zoology) Putting the whole foot upon the ground in walking, as some mammals do

    https://wikidiff.com/plantigrade/palmigrade

    https://en.m.wikipedia.org/wiki/Plantigrade
    Plantigrade mammal species include (but are not limited to):
    Some primates (including humans)
    Ailuridae: red pandas
    Ursidae: bears
    Ok. I too am unfamiliar with the distinction between palmigrade and
    plantigrade. One source I found said "palmigrade" is an adjective and
    "plantigrade" is a noun, but that just adds to the confusion.
    Yes, both can be noun or adjective as needed, -grade, -grady.
    Anatomically, the relevant distinction is how much of the foot rests
    on the ground when walking, either plantigrade, digitigrade or
    unguligrade.
    Yes. Knucklewalking fits in-between, plantigrade hind limbs & digitigrade (dorsal) forelimbs.
    My understanding is those terms apply equally to both forelimbs and hindlimbs.
    Yes. Knucklewalking doesn't afaik.

    For primates, the importance of fingers as manipulating tools means
    they necessarily compromise the hand's anatomy for locomotion. For
    arboreal primates, the phalanges are curved to better grasp branches.
    For quadruped primates, the hands may be flat on the ground as with
    baboons. Facultative bipedal primates may use knuckle-walking as with
    chimpanzees.
    Yes. Rainforest drills have shortish fingers, they walk on their fingertips not palms.
    For obligate bipeds like genus homo, the hands aren't used for
    locomotion at all, and their anatomy is devoted to manipulation. My
    understanding is genus australopithecus are transitional between
    arboreal bipedal primates and terrestrial bipedal primates.
    I liked this Sci Am article, especially near the end, section called Open Question.
    https://www.scientificamerican.com/article/fossils-upend-conventional-wisdom-about-evolution-of-human-bipedalism/
    Thanks for the link. Are you familiar with a book called "Contested
    Bones"? Erika does a multi-part and extremely detailed critique of
    it.

    I'll watch when I get time. Hurricane Nicole is coming around.

    I don't know enough about Miocene apes to say if European and African
    apes were different. My understanding is climate change caused >> >> >> >> European Miocene apes to go extinct before Australopiths evolved in
    Africa, which suggests to me the two environments were different >> >> >> >> enough to support the differences you describe.

    I opine that European Miocene apes expanded from the Black Sea region after the MSC, some of their descendants included australopiths, Homo etc. entering Africa in waves.

    At 7:20, she apparently claims that chimp and gorilla arboreal traits interfere with their terrestrial locomotion "act to negate bipedalism" No, sleeping in bowl nests did that, selecting for short legs & backs.
    https://youtu.be/jo2ZLnucuHY?t=451
    Erika says this:
    *********************************************
    Either way, the aspects that allow for arboriality found in
    australopithecus afarensis are not the same types as the ones that we
    find in chimpanzees and gorillas. In the latter two species, the >> >> >> >> arboreal aspects

    I guess 'aspect' could include arboreal bowl nesting, I thought she meant arboreal locomotion only.

    act to negate efficient bipedality,

    Not arboreal hylobatids. Bowl sleeping in great apes shrank their leg, achilles & back length.
    My understanding is, when Erika refers to bipedality without
    qualifiers, she means terrestrial bipedality.
    whereas in
    australopithecus afarensis they're sort of removed from it.

    The key is whether australopiths & kin had halluces that could swivel outwardly while branch-walking and swivel inwardly while ground-walking.
    Erika persuasively argues that an outward hallux would help to
    stabilize a not-fully-developed terrestrial bipedal stance.

    I presume that an "outward hallux" is a divergent hallux. That may differ from one that can swivel in or out per need. One that permanently stays divergent is a walking hazard, constantly snagging on vegetation, and would likely be selected
    against in a biped. Our toes have shortened, halluces converged, while our soles have lengthened providing postural stability.
    My understanding is the primitive hallux was anatomically similar to >> >> the pollex, in that it was opposable under voluntary muscular control. >> >> So an "outward" (your word) hallux would not have been an impediment >> >> to walking on the ground. To the contrary, such a feature would be
    advantageous to organisms which moved both terrestrially and
    arboreally.

    As you say, modern humans have shortened parallel toes, a derived
    specialization for efficiently walking long distance on the ground.
    Personally, I can with difficulty move my big toes only a little in
    and out, like some crippled crab. However, I have a good friend who
    can move her big toes substantially and strongly, enough to painfully >> >> pinch other people's legs under the table while playing card games, to >> >> good strategic effect.
    :~}
    They
    allow for arboreal behaviors when necessary but don't
    harm the effectiveness of bipedality when the animal came down to the
    ground.
    *********************************************

    Erika doesn't argue the cause for these arboreal aspects, but only
    that their presence in chimpanzees and gorillas inhibits efficient
    bipedality. Anybody who has seen videos of gorillas and chimpanzees
    walking bipedally would agree they are much less efficient at it than
    are humans. Erika's point in paraphrase is that Lucy had a big butt, I
    cannot lie, and so walked more like humans do.

    Consider my earlier point about Homo erectus: thick heavy femur and skull occiput mechanically improved balance and pace while ground-walking orthogonally; this continued with neanderthals with pronounced occipital bun (bone + enlarged
    posteriorly cerebrum) and wide hips (Venus figurines?) and with Homo sapiens (software replaced mechanistic balancing, except in Khoisan and Andamaner females with very posterior buttocks (steatopygia), selected by long distance trekking.

    I wanted to go in depth on this video, but there is a massive noisy halloween celebration of trick or treating goblins and princesses here at the library. So enough.
    I hope you find time once the ghosts and goblins have gone.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to All on Wed Nov 16 11:08:08 2022
    On Fri, 04 Nov 2022 02:21:55 -0400, jillery <69jpil69@gmail.com>
    wrote:

    On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden
    <daud.deden@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote: >>> On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the >>> >> >> latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in >>> >> >> central-african Chad, and also because it may be the oldest bipedal >>> >> >> hominin fossil found to date. However, there appears to be strong >>> >> >> disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism. >>> >> >> She discusses several hypotheses, and presents compelling arguments >>> >> >> for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a
    Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.


    My impression is there isn't enough evidence to show whether Pliocene
    African apes descended from Miocene European apes or Miocene African
    apes. Either way, there was enough time between the two eras to have
    evolved differences between either Miocene populations and Pliocene S. >tchadensis.


    I have recently become aware of:

    <https://en.wikipedia.org/wiki/Danuvius_guggenmosi>

    which was a Miocene European ape that may have evolved arboreal
    bipedalism similar to S.tchadensis.

    Depending on how widespread its range, and how successful its
    descendants, it's plausible they lived south of the Black Sea during
    the late Miocene.

    The question then becomes whether it's more likely these apes found
    their way into Africa to become the ancestors of Pliocene
    S.tchadensis, or whether S.tchadensis evolved from Miocene African
    apes.

    Unfortunately, the habitat of these apes made their fossil
    preservation extremely rare, and so the evidence to well support
    either hypothesis is lacking.

    However, the question at least conditionally can be answered by
    comparing the likelihood of a migratory pathway during that time,
    versus the likelihood of arboreal bipedalism evolving independently in
    two populations.

    There are a number of anatomic features associated with arboreal
    bipedalism, some of which are necessary, ex. anterior foramen magnum,
    and some of which are incidental, ex. molar patterns. Descendant
    populations are more likely to share these features than are
    independent populations. This suggests to me that a sufficiently
    robust fossil record could answer this question with some degree of
    certainty.

    Alternately, my understanding is southern Europe and central Africa
    are ecological opposites, in the sense that when one is hot and dry
    the other is temperate and wet. This is as true now as it was in the
    Miocene. This suggests to me there could not have been an unbroken
    forested path for arboreal apes to migrate between Europe/Near East
    and Central Africa.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Wed Nov 16 22:29:02 2022
    On Wednesday, November 16, 2022 at 11:08:11 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 04 Nov 2022 02:21:55 -0400, jillery <69jp...@gmail.com>
    wrote:

    On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the >>> >> >> latest developments relating to the origins of human bipedalism: >>> >> >>
    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong >>> >> >> disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a
    Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.


    My impression is there isn't enough evidence to show whether Pliocene >African apes descended from Miocene European apes or Miocene African
    apes. Either way, there was enough time between the two eras to have >evolved differences between either Miocene populations and Pliocene S. >tchadensis.
    I have recently become aware of:

    <https://en.wikipedia.org/wiki/Danuvius_guggenmosi>

    which was a Miocene European ape that may have evolved arboreal
    bipedalism similar to S.tchadensis.

    Depending on how widespread its range, and how successful its
    descendants, it's plausible they lived south of the Black Sea during
    the late Miocene.

    The question then becomes whether it's more likely these apes found
    their way into Africa to become the ancestors of Pliocene
    S.tchadensis, or whether S.tchadensis evolved from Miocene African
    apes.

    Unfortunately, the habitat of these apes made their fossil
    preservation extremely rare, and so the evidence to well support
    either hypothesis is lacking.

    However, the question at least conditionally can be answered by
    comparing the likelihood of a migratory pathway during that time,
    versus the likelihood of arboreal bipedalism evolving independently in
    two populations.

    There are a number of anatomic features associated with arboreal
    bipedalism, some of which are necessary, ex. anterior foramen magnum,

    4
    The foramen magnum is always situated relatively more anteriorly in immature than in mature apes and men.

    and some of which are incidental, ex. molar patterns. Descendant
    populations are more likely to share these features than are
    independent populations. This suggests to me that a sufficiently
    robust fossil record could answer this question with some degree of certainty.

    Alternately, my understanding is southern Europe and central Africa
    are ecological opposites, in the sense that when one is hot and dry
    the other is temperate and wet.

    Central Africa is and was hot, the southern Black Sea is between temperate and tropical.

    This is as true now as it was in the
    Miocene. This suggests to me there could not have been an unbroken
    forested path for arboreal apes to migrate between Europe/Near East
    and Central Africa.

    I would not claim nor disclaim that. The Levant is near the midpoint, extends the African Rift valley to Anatolia, is a major avian migration route between Africa and Eurasia, has fossil/artifacts of Homo erectus, neanderthal & sapiens oldest known
    cooking (fish .78ma) and earliest waternut gathering and bread making. The region is amenable to hominins & Homo.

    Danuvius, Rudapithecus, Graecopithecus, Oranopithecus each had a unique trait shared with hominins. I think of them as a superspecies with local variations.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to Daud Deden on Wed Nov 16 22:42:03 2022
    On Thursday, November 17, 2022 at 1:29:04 AM UTC-5, Daud Deden wrote:
    On Wednesday, November 16, 2022 at 11:08:11 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 04 Nov 2022 02:21:55 -0400, jillery <69jp...@gmail.com>
    wrote:

    On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism: >>> >> >>
    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY >>> >> Thank you for citing the above video. It's prelude to the ones I >>> >> cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a >>> Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.


    My impression is there isn't enough evidence to show whether Pliocene >African apes descended from Miocene European apes or Miocene African >apes. Either way, there was enough time between the two eras to have >evolved differences between either Miocene populations and Pliocene S. >tchadensis.
    I have recently become aware of:

    <https://en.wikipedia.org/wiki/Danuvius_guggenmosi>

    which was a Miocene European ape that may have evolved arboreal
    bipedalism similar to S.tchadensis.

    Depending on how widespread its range, and how successful its
    descendants, it's plausible they lived south of the Black Sea during
    the late Miocene.

    The question then becomes whether it's more likely these apes found
    their way into Africa to become the ancestors of Pliocene
    S.tchadensis, or whether S.tchadensis evolved from Miocene African
    apes.

    Unfortunately, the habitat of these apes made their fossil
    preservation extremely rare, and so the evidence to well support
    either hypothesis is lacking.

    However, the question at least conditionally can be answered by
    comparing the likelihood of a migratory pathway during that time,
    versus the likelihood of arboreal bipedalism evolving independently in
    two populations.

    There are a number of anatomic features associated with arboreal bipedalism, some of which are necessary, ex. anterior foramen magnum,
    4
    The foramen magnum is always situated relatively more anteriorly in immature than in mature apes and men.
    and some of which are incidental, ex. molar patterns. Descendant populations are more likely to share these features than are
    independent populations. This suggests to me that a sufficiently
    robust fossil record could answer this question with some degree of certainty.

    Alternately, my understanding is southern Europe and central Africa
    are ecological opposites, in the sense that when one is hot and dry
    the other is temperate and wet.
    Central Africa is and was hot, the southern Black Sea is between temperate and tropical.
    This is as true now as it was in the
    Miocene. This suggests to me there could not have been an unbroken forested path for arboreal apes to migrate between Europe/Near East
    and Central Africa.
    I would not claim nor disclaim that. The Levant is near the midpoint, extends the African Rift valley to Anatolia, is a major avian migration route between Africa and Eurasia, has fossil/artifacts of Homo erectus, neanderthal & sapiens oldest known
    cooking (fish .78ma) and earliest waternut gathering and bread making. The region is amenable to hominins & Homo.

    Danuvius, Rudapithecus, Graecopithecus, Oranopithecus each had a unique trait shared with hominins. I think of them as a superspecies with local variations.
    -
    If you place Danuvius half-way between fast brachiating bipedal long backed long achilles tendon hylobatids and bipedal Homo with long back and long achilles tendon, it fits perfectly.

    Wiki:
    Danuvius is thought to have had a broad chest. It is the first recorded Miocene great ape to have had the diaphragm located in the lower chest cavity, as in Homo, indicating an extended lower back and a greater number of functional lumbar vertebrae. This
    may have caused lordosis (the normal curvature of the human spine) and moved the center of mass over the hips and legs, which implies some habitual bipedal activity.

    The robust finger and hypertrophied wrist and elbow bones indicate a strong grip and load bearing adaptations for the arms. The legs also show adaptations for load-bearing, especially at the hypertrophied knee joint. There was likely limited ankle
    loading, and the ankle would have had a hinge-like function, being most stable if positioned perpendicularly to the leg as opposed to at an angle in apes. Danuvius was likely able to achieve a strong grip with its big toes, unlike modern African great
    apes, which would have allowed it to grasp onto thinner trees. The limb proportions are most similar to those of bonobos.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to daud.deden@gmail.com on Thu Nov 17 12:57:55 2022
    On Wed, 16 Nov 2022 22:42:03 -0800 (PST), Daud Deden
    <daud.deden@gmail.com> wrote:

    On Thursday, November 17, 2022 at 1:29:04 AM UTC-5, Daud Deden wrote:
    On Wednesday, November 16, 2022 at 11:08:11 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 04 Nov 2022 02:21:55 -0400, jillery <69jp...@gmail.com>
    wrote:

    On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY >> > >>> >> Thank you for citing the above video. It's prelude to the ones I >> > >>> >> cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a >> > >>> Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.


    My impression is there isn't enough evidence to show whether Pliocene
    African apes descended from Miocene European apes or Miocene African
    apes. Either way, there was enough time between the two eras to have
    evolved differences between either Miocene populations and Pliocene S. >> > >tchadensis.

    I have recently become aware of:

    <https://en.wikipedia.org/wiki/Danuvius_guggenmosi>

    which was a Miocene European ape that may have evolved arboreal
    bipedalism similar to S.tchadensis.

    Depending on how widespread its range, and how successful its
    descendants, it's plausible they lived south of the Black Sea during
    the late Miocene.

    The question then becomes whether it's more likely these apes found
    their way into Africa to become the ancestors of Pliocene
    S.tchadensis, or whether S.tchadensis evolved from Miocene African
    apes.

    Unfortunately, the habitat of these apes made their fossil
    preservation extremely rare, and so the evidence to well support
    either hypothesis is lacking.

    However, the question at least conditionally can be answered by
    comparing the likelihood of a migratory pathway during that time,
    versus the likelihood of arboreal bipedalism evolving independently in
    two populations.

    There are a number of anatomic features associated with arboreal
    bipedalism, some of which are necessary, ex. anterior foramen magnum,

    The foramen magnum is always situated relatively more anteriorly in immature than in mature apes and men.


    Not sure what you mean by "mature"; the individual or the species?
    Either way, the important point is the position and angle of foramen
    magnum are diagnostic among all vertebrates for how they habitually
    hold their head, and so includes/excludes bipedalism among hominids.


    and some of which are incidental, ex. molar patterns. Descendant
    populations are more likely to share these features than are
    independent populations. This suggests to me that a sufficiently
    robust fossil record could answer this question with some degree of
    certainty.

    Alternately, my understanding is southern Europe and central Africa
    are ecological opposites, in the sense that when one is hot and dry
    the other is temperate and wet.
    Central Africa is and was hot,


    ... and wet aka tropical, just right for the evolution of small
    bipedal arboreal apes.


    the southern Black Sea is between temperate and tropical.


    Correct. Southern Europe and the Black Sea are at the same latitudes.
    This suggests they would tend to have the same climate. However, the
    Black Sea is farther inland, and so suffers more continental extremes.
    So any climate changes will appear first around the Black Sea and
    become more extreme compared to southern Europe.

    Moving toward 30 degrees latitude, rainfall becomes seasonally dry,
    and then almost continuously dry. My understanding is, the only
    native forests south of the Caspian are in the mountains, and adjacent
    to the Mediterranean coasts. Arboreal apes of any kind would find
    these deserts impassible.

    To a first approximation, average rainfall and temperature are
    functions of latitude. However, while temperature is a function of
    the sine of latitude, rainfall is more complex. It tends to be
    continuously heavy near the equator, continuously dry near 30 degrees,
    and seasonally variable between 30 and 60 degrees. This general
    pattern is modified, sometimes dramatically, by terrain, ocean
    currents, seasons, and Milankovitch cycles.

    The most significant variable is Africa's northward tectonic
    migration, about a centimeter a year since before the Miocene. So,
    while central Africa has moved from south to north of the equator with
    little effect, north Africa has approached and then went north of 30
    degrees, making it over time ever drier, amplifying other climate
    trends, making once wooded areas into vast savannah and desert.

    Also, Africa's tectonic slide north almost certainly pinched closed
    the Gilbraltar Sttraits, which caused the Mediterranean to dry up at
    least once, and likely several times as sea levels rose and fell. The resulting hot salt basin would also have been impassible for arboreal
    apes.


    This is as true now as it was in the
    Miocene. This suggests to me there could not have been an unbroken
    forested path for arboreal apes to migrate between Europe/Near East
    and Central Africa.
    I would not claim nor disclaim that. The Levant is near the midpoint, extends the African Rift valley to Anatolia, is a major avian migration route between Africa and Eurasia, has fossil/artifacts of Homo erectus, neanderthal & sapiens oldest known
    cooking (fish .78ma) and earliest waternut gathering and bread making. The region is amenable to hominins & Homo.


    I acknowledge the facts you describe above. However, the Levant is
    savannah and desert except for a narrow strip along the Mediterranean
    and up in the mountains. While this is no problem for terrestrial
    bipeds like Homo, ISTM arboreal hominids like D.guggenmosi would have
    a much harder time living/migrating there.


    Danuvius, Rudapithecus, Graecopithecus, Oranopithecus each had a unique trait shared with hominins. I think of them as a superspecies with local variations.
    -
    If you place Danuvius half-way between fast brachiating bipedal long backed long achilles tendon hylobatids and bipedal Homo with long back and long achilles tendon, it fits perfectly.

    Wiki:
    Danuvius is thought to have had a broad chest. It is the first recorded Miocene great ape to have had the diaphragm located in the lower chest cavity, as in Homo, indicating an extended lower back and a greater number of functional lumbar vertebrae.
    This may have caused lordosis (the normal curvature of the human spine) and moved the center of mass over the hips and legs, which implies some habitual bipedal activity.

    The robust finger and hypertrophied wrist and elbow bones indicate a strong grip and load bearing adaptations for the arms. The legs also show adaptations for load-bearing, especially at the hypertrophied knee joint. There was likely limited ankle
    loading, and the ankle would have had a hinge-like function, being most stable if positioned perpendicularly to the leg as opposed to at an angle in apes. Danuvius was likely able to achieve a strong grip with its big toes, unlike modern African great
    apes, which would have allowed it to grasp onto thinner trees. The limb proportions are most similar to those of bonobos.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Thu Nov 17 15:53:51 2022
    On Thursday, November 17, 2022 at 12:57:57 PM UTC-5, 69jp...@gmail.com wrote:
    On Wed, 16 Nov 2022 22:42:03 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 1:29:04 AM UTC-5, Daud Deden wrote:
    On Wednesday, November 16, 2022 at 11:08:11 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 04 Nov 2022 02:21:55 -0400, jillery <69jp...@gmail.com>
    wrote:

    On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is >> > >>> >> >> remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY >> > >>> >> Thank you for citing the above video. It's prelude to the ones I >> > >>> >> cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a >> > >>> Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.


    My impression is there isn't enough evidence to show whether Pliocene >> > >African apes descended from Miocene European apes or Miocene African >> > >apes. Either way, there was enough time between the two eras to have >> > >evolved differences between either Miocene populations and Pliocene S. >> > >tchadensis.

    I have recently become aware of:

    <https://en.wikipedia.org/wiki/Danuvius_guggenmosi>

    which was a Miocene European ape that may have evolved arboreal
    bipedalism similar to S.tchadensis.

    Depending on how widespread its range, and how successful its
    descendants, it's plausible they lived south of the Black Sea during
    the late Miocene.

    The question then becomes whether it's more likely these apes found
    their way into Africa to become the ancestors of Pliocene
    S.tchadensis, or whether S.tchadensis evolved from Miocene African
    apes.

    Unfortunately, the habitat of these apes made their fossil
    preservation extremely rare, and so the evidence to well support
    either hypothesis is lacking.

    However, the question at least conditionally can be answered by
    comparing the likelihood of a migratory pathway during that time,
    versus the likelihood of arboreal bipedalism evolving independently in >> > two populations.

    There are a number of anatomic features associated with arboreal
    bipedalism, some of which are necessary, ex. anterior foramen magnum, >>
    The foramen magnum is always situated relatively more anteriorly in immature than in mature apes and men.
    Not sure what you mean by "mature"; the individual or the species?

    Individually.

    Either way, the important point is the position and angle of foramen
    magnum are diagnostic among all vertebrates for how they habitually
    hold their head, and so includes/excludes bipedalism among hominids.

    Yes, but no. Great apes are bipedal except when (hurrying) on open ground they adopt quadrupedalism. Homo retains the primitive bipedal gait of hominoid ancestors, as do hylobatids.

    and some of which are incidental, ex. molar patterns. Descendant
    populations are more likely to share these features than are
    independent populations. This suggests to me that a sufficiently
    robust fossil record could answer this question with some degree of
    certainty.

    Alternately, my understanding is southern Europe and central Africa
    are ecological opposites, in the sense that when one is hot and dry
    the other is temperate and wet.
    Central Africa is and was hot,
    ... and wet aka tropical,

    The adoption of qpal knucklewalking by African apes indicates that their ancient habitat went through a dry phase (rainforest became patchy) forcing a terrestrial dog-like gait.

    just right for the evolution of small
    bipedal arboreal apes.

    The fact that there are no small bipedal arboreal apes in Africa indicates that there was some climate shifting.

    the southern Black Sea is between temperate and tropical.
    Correct. Southern Europe and the Black Sea are at the same latitudes.
    This suggests they would tend to have the same climate. However, the
    Black Sea is farther inland, and so suffers more continental extremes.
    So any climate changes will appear first around the Black Sea and
    become more extreme compared to southern Europe.

    I'm talking about from 11ma through the MSC to 5ma. The Medit. & Red Seas dried out, the Black Sea didn't.

    Moving toward 30 degrees latitude, rainfall becomes seasonally dry,
    and then almost continuously dry. My understanding is, the only
    native forests south of the Caspian are in the mountains, and adjacent
    to the Mediterranean coasts. Arboreal apes of any kind would find
    these deserts impassible.

    You are speaking of recent climate. There are no arboreal apes there now.

    To a first approximation, average rainfall and temperature are
    functions of latitude. However, while temperature is a function of
    the sine of latitude, rainfall is more complex. It tends to be
    continuously heavy near the equator, continuously dry near 30 degrees,
    and seasonally variable between 30 and 60 degrees. This general
    pattern is modified, sometimes dramatically, by terrain, ocean
    currents, seasons, and Milankovitch cycles.

    The most significant variable is Africa's northward tectonic
    migration, about a centimeter a year since before the Miocene. So,
    while central Africa has moved from south to north of the equator with little effect, north Africa has approached and then went north of 30 degrees, making it over time ever drier, amplifying other climate
    trends, making once wooded areas into vast savannah and desert.

    Yes.

    Also, Africa's tectonic slide north almost certainly pinched closed
    the Gilbraltar Sttraits, which caused the Mediterranean to dry up at
    least once, and likely several times as sea levels rose and fell. The resulting hot salt basin would also have been impassible for arboreal
    apes.
    This is as true now as it was in the
    Miocene. This suggests to me there could not have been an unbroken
    forested path for arboreal apes to migrate between Europe/Near East
    and Central Africa.
    I would not claim nor disclaim that. The Levant is near the midpoint, extends the African Rift valley to Anatolia, is a major avian migration route between Africa and Eurasia, has fossil/artifacts of Homo erectus, neanderthal & sapiens oldest known
    cooking (fish .78ma) and earliest waternut gathering and bread making. The region is amenable to hominins & Homo.
    I acknowledge the facts you describe above. However, the Levant is
    savannah and desert except for a narrow strip along the Mediterranean
    and up in the mountains. While this is no problem for terrestrial
    bipeds like Homo, ISTM arboreal hominids like D.guggenmosi would have
    a much harder time living/migrating there.

    "is". Again, refer to microclimate of Levant 11ma - 5ma. Today's Dead Sea was once the vast brackish Lake Lisan that reached to Lebanon, a gallery forest may have reached from Anatolia to Egypt.
    What is ISTM?

    Danuvius, Rudapithecus, Graecopithecus, Oranopithecus each had a unique trait shared with hominins. I think of them as a superspecies with local variations.
    -
    If you place Danuvius half-way between fast brachiating bipedal long backed long achilles tendon hylobatids and bipedal Homo with long back and long achilles tendon, it fits perfectly.

    Wiki:
    Danuvius is thought to have had a broad chest. It is the first recorded Miocene great ape to have had the diaphragm located in the lower chest cavity, as in Homo, indicating an extended lower back and a greater number of functional lumbar vertebrae.
    This may have caused lordosis (the normal curvature of the human spine) and moved the center of mass over the hips and legs, which implies some habitual bipedal activity.

    The robust finger and hypertrophied wrist and elbow bones indicate a strong grip and load bearing adaptations for the arms. The legs also show adaptations for load-bearing, especially at the hypertrophied knee joint. There was likely limited ankle
    loading, and the ankle would have had a hinge-like function, being most stable if positioned perpendicularly to the leg as opposed to at an angle in apes. Danuvius was likely able to achieve a strong grip with its big toes, unlike modern African great
    apes, which would have allowed it to grasp onto thinner trees. The limb proportions are most similar to those of bonobos.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to Daud Deden on Thu Nov 17 22:08:36 2022
    On Thursday, November 17, 2022 at 6:53:53 PM UTC-5, Daud Deden wrote:
    On Thursday, November 17, 2022 at 12:57:57 PM UTC-5, 69jp...@gmail.com wrote:
    On Wed, 16 Nov 2022 22:42:03 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 1:29:04 AM UTC-5, Daud Deden wrote:
    On Wednesday, November 16, 2022 at 11:08:11 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 04 Nov 2022 02:21:55 -0400, jillery <69jp...@gmail.com>
    wrote:

    On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy. >> > >>> >
    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a
    Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.


    My impression is there isn't enough evidence to show whether Pliocene
    African apes descended from Miocene European apes or Miocene African >> > >apes. Either way, there was enough time between the two eras to have >> > >evolved differences between either Miocene populations and Pliocene S.
    tchadensis.

    I have recently become aware of:

    <https://en.wikipedia.org/wiki/Danuvius_guggenmosi>

    which was a Miocene European ape that may have evolved arboreal
    bipedalism similar to S.tchadensis.

    Depending on how widespread its range, and how successful its
    descendants, it's plausible they lived south of the Black Sea during >> > the late Miocene.

    The question then becomes whether it's more likely these apes found >> > their way into Africa to become the ancestors of Pliocene
    S.tchadensis, or whether S.tchadensis evolved from Miocene African
    apes.

    Unfortunately, the habitat of these apes made their fossil
    preservation extremely rare, and so the evidence to well support
    either hypothesis is lacking.

    However, the question at least conditionally can be answered by
    comparing the likelihood of a migratory pathway during that time,
    versus the likelihood of arboreal bipedalism evolving independently in
    two populations.

    There are a number of anatomic features associated with arboreal
    bipedalism, some of which are necessary, ex. anterior foramen magnum, >>
    The foramen magnum is always situated relatively more anteriorly in immature than in mature apes and men.
    Not sure what you mean by "mature"; the individual or the species?
    Individually.
    Either way, the important point is the position and angle of foramen magnum are diagnostic among all vertebrates for how they habitually
    hold their head, and so includes/excludes bipedalism among hominids.
    Yes, but no. Great apes are bipedal except when (hurrying) on open ground they adopt quadrupedalism. Homo retains the primitive bipedal gait of hominoid ancestors, as do hylobatids.
    and some of which are incidental, ex. molar patterns. Descendant
    populations are more likely to share these features than are
    independent populations. This suggests to me that a sufficiently
    robust fossil record could answer this question with some degree of >> > certainty.

    Alternately, my understanding is southern Europe and central Africa >> > are ecological opposites, in the sense that when one is hot and dry >> > the other is temperate and wet.
    Central Africa is and was hot,
    ... and wet aka tropical,
    The adoption of qpal knucklewalking by African apes indicates that their ancient habitat went through a dry phase (rainforest became patchy) forcing a terrestrial dog-like gait.
    just right for the evolution of small
    bipedal arboreal apes.
    The fact that there are no small bipedal arboreal apes in Africa indicates that there was some climate shifting.
    the southern Black Sea is between temperate and tropical.
    Correct. Southern Europe and the Black Sea are at the same latitudes.
    This suggests they would tend to have the same climate. However, the
    Black Sea is farther inland, and so suffers more continental extremes.
    So any climate changes will appear first around the Black Sea and
    become more extreme compared to southern Europe.
    I'm talking about from 11ma through the MSC to 5ma. The Medit. & Red Seas dried out, the Black Sea didn't.
    Moving toward 30 degrees latitude, rainfall becomes seasonally dry,
    and then almost continuously dry. My understanding is, the only
    native forests south of the Caspian are in the mountains, and adjacent
    to the Mediterranean coasts. Arboreal apes of any kind would find
    these deserts impassible.
    You are speaking of recent climate. There are no arboreal apes there now.
    To a first approximation, average rainfall and temperature are
    functions of latitude. However, while temperature is a function of
    the sine of latitude, rainfall is more complex. It tends to be continuously heavy near the equator, continuously dry near 30 degrees,
    and seasonally variable between 30 and 60 degrees. This general
    pattern is modified, sometimes dramatically, by terrain, ocean
    currents, seasons, and Milankovitch cycles.

    The most significant variable is Africa's northward tectonic
    migration, about a centimeter a year since before the Miocene. So,
    while central Africa has moved from south to north of the equator with little effect, north Africa has approached and then went north of 30 degrees, making it over time ever drier, amplifying other climate
    trends, making once wooded areas into vast savannah and desert.
    Yes.
    Also, Africa's tectonic slide north almost certainly pinched closed
    the Gilbraltar Sttraits, which caused the Mediterranean to dry up at
    least once, and likely several times as sea levels rose and fell. The resulting hot salt basin would also have been impassible for arboreal apes.
    This is as true now as it was in the
    Miocene. This suggests to me there could not have been an unbroken
    forested path for arboreal apes to migrate between Europe/Near East >> > and Central Africa.
    I would not claim nor disclaim that. The Levant is near the midpoint, extends the African Rift valley to Anatolia, is a major avian migration route between Africa and Eurasia, has fossil/artifacts of Homo erectus, neanderthal & sapiens oldest
    known cooking (fish .78ma) and earliest waternut gathering and bread making. The region is amenable to hominins & Homo.
    I acknowledge the facts you describe above. However, the Levant is savannah and desert except for a narrow strip along the Mediterranean
    and up in the mountains. While this is no problem for terrestrial
    bipeds like Homo, ISTM arboreal hominids like D.guggenmosi would have
    a much harder time living/migrating there.
    "is". Again, refer to microclimate of Levant 11ma - 5ma. Today's Dead Sea was once the vast brackish Lake Lisan that reached to Lebanon, a gallery forest may have reached from Anatolia to Egypt.
    What is ISTM?
    Danuvius, Rudapithecus, Graecopithecus, Oranopithecus each had a unique trait shared with hominins. I think of them as a superspecies with local variations.
    -
    If you place Danuvius half-way between fast brachiating bipedal long backed long achilles tendon hylobatids and bipedal Homo with long back and long achilles tendon, it fits perfectly.

    Wiki:
    Danuvius is thought to have had a broad chest. It is the first recorded Miocene great ape to have had the diaphragm located in the lower chest cavity, as in Homo, indicating an extended lower back and a greater number of functional lumbar vertebrae.
    This may have caused lordosis (the normal curvature of the human spine) and moved the center of mass over the hips and legs, which implies some habitual bipedal activity.

    The robust finger and hypertrophied wrist and elbow bones indicate a strong grip and load bearing adaptations for the arms. The legs also show adaptations for load-bearing, especially at the hypertrophied knee joint. There was likely limited ankle
    loading, and the ankle would have had a hinge-like function, being most stable if positioned perpendicularly to the leg as opposed to at an angle in apes. Danuvius was likely able to achieve a strong grip with its big toes, unlike modern African great
    apes, which would have allowed it to grasp onto thinner trees. The limb proportions are most similar to those of bonobos.
    -
    Add.

    The latest version of Lake Lisan existed between 70ka and 12ka. What existed there between 10ma and 5ma? Was there a lake during wetter periods? Was the Dead Sea transform/rift as attractive to hominids as the African rift valley?
    I'm not knowledgeable about the ancient ecology, but it seems to me that when the Arabian peninsula had inland lakes and the Sahara had green periods with hominins, the lake could have extended to the Gulf of Aqaba of the Red Sea. African hyrax may have
    followed it?

    https://www.geoexpro.com/articles/2019/12/the-dead-sea-transform

    We were excited to explore the sedimentary evidence of ancient earthquakes hidden in obscure arroyos cut through the Lisan Formation below the mountain. This formation consists of varves deposited between 70,000 and 12,000 years ago in Lake Lisan, a
    larger version of the Dead Sea that also encompassed today’s Sea of Galilee. Identical millimetre-thick varve couplets accumulate on the floor of today’s Dead Sea, composed of clastic detritus that washes into the lake during winter storms,
    alternating with aragonite that precipitates during intense summer evaporation. In places the Lisan Formation’s varves are interbedded with fractured and folded beds that record sediment liquefaction and slumping that occurred during an ancient
    earthquake. Scientists have used these ‘seismites’ to construct a 50,000-year earthquake record for the Dead Sea Transform, the longest continuous such record on Earth.

    Human and Geological Monuments
    The lush oasis of Ein Gedi is perched on the banks of the Dead Sea 21km north of Masada. Here two fault-controlled canyons carved by spring-fed streams crease the Judean Plateau. The streams tumble down beautiful, travertine-encrusted waterfalls and
    sustain local wildlife, including hyrax and Nubian ibex, in the otherwise harsh and unforgiving landscape.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to daud.deden@gmail.com on Fri Nov 18 02:12:32 2022
    On Thu, 17 Nov 2022 15:53:51 -0800 (PST), Daud Deden
    <daud.deden@gmail.com> wrote:

    On Thursday, November 17, 2022 at 12:57:57 PM UTC-5, 69jp...@gmail.com wrote: >> On Wed, 16 Nov 2022 22:42:03 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 1:29:04 AM UTC-5, Daud Deden wrote:
    On Wednesday, November 16, 2022 at 11:08:11 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 04 Nov 2022 02:21:55 -0400, jillery <69jp...@gmail.com>
    wrote:

    On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is >> >> > >>> >> >> remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy. >> >> > >>> >
    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a
    Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.


    My impression is there isn't enough evidence to show whether Pliocene >> >> > >African apes descended from Miocene European apes or Miocene African >> >> > >apes. Either way, there was enough time between the two eras to have >> >> > >evolved differences between either Miocene populations and Pliocene S.
    tchadensis.

    I have recently become aware of:

    <https://en.wikipedia.org/wiki/Danuvius_guggenmosi>

    which was a Miocene European ape that may have evolved arboreal
    bipedalism similar to S.tchadensis.

    Depending on how widespread its range, and how successful its
    descendants, it's plausible they lived south of the Black Sea during >> >> > the late Miocene.

    The question then becomes whether it's more likely these apes found
    their way into Africa to become the ancestors of Pliocene
    S.tchadensis, or whether S.tchadensis evolved from Miocene African
    apes.

    Unfortunately, the habitat of these apes made their fossil
    preservation extremely rare, and so the evidence to well support
    either hypothesis is lacking.

    However, the question at least conditionally can be answered by
    comparing the likelihood of a migratory pathway during that time,
    versus the likelihood of arboreal bipedalism evolving independently in >> >> > two populations.

    There are a number of anatomic features associated with arboreal
    bipedalism, some of which are necessary, ex. anterior foramen magnum, >> >>
    The foramen magnum is always situated relatively more anteriorly in immature than in mature apes and men.
    Not sure what you mean by "mature"; the individual or the species?

    Individually.


    My understanding is the relative position of foramen magnum doesn't
    change significantly during human development.


    Either way, the important point is the position and angle of foramen
    magnum are diagnostic among all vertebrates for how they habitually
    hold their head, and so includes/excludes bipedalism among hominids.

    Yes, but no. Great apes are bipedal except when (hurrying) on open ground they adopt quadrupedalism. Homo retains the primitive bipedal gait of hominoid ancestors, as do hylobatids.


    All Homo species are great apes by definition, including H.sapiens.
    They do/did quadrupedalism only in exceptional cases.


    and some of which are incidental, ex. molar patterns. Descendant
    populations are more likely to share these features than are
    independent populations. This suggests to me that a sufficiently
    robust fossil record could answer this question with some degree of
    certainty.

    Alternately, my understanding is southern Europe and central Africa
    are ecological opposites, in the sense that when one is hot and dry
    the other is temperate and wet.
    Central Africa is and was hot,
    ... and wet aka tropical,

    The adoption of qpal knucklewalking by African apes indicates that their ancient habitat went through a dry phase (rainforest became patchy) forcing a terrestrial dog-like gait.


    Perhaps. My understanding is bipedal arboreal apes continued to walk
    bipedally on the ground, while non-bipedal arboreal apes also adopted quadrupedal habits on the ground.


    just right for the evolution of small bipedal arboreal apes.

    The fact that there are no small bipedal arboreal apes in Africa indicates that there was some climate shifting.


    Again perhaps. It also suggests small bipedal arboreal apes were
    outcompeted.


    the southern Black Sea is between temperate and tropical.
    Correct. Southern Europe and the Black Sea are at the same latitudes.
    This suggests they would tend to have the same climate. However, the
    Black Sea is farther inland, and so suffers more continental extremes.
    So any climate changes will appear first around the Black Sea and
    become more extreme compared to southern Europe.

    I'm talking about from 11ma through the MSC to 5ma. The Medit. & Red Seas dried out, the Black Sea didn't.


    The relative position of the Black Sea didn't change from then to now.
    The important point is its position is deep in Eurasia, where
    continental climates rule.

    My understanding is the Mediterranean dried out only about 6mya, long
    after European, and presumably Black Sea, arboreal apes went extinct.

    The Red Sea is too far south to affect migration from Europe to Africa regardless of climate patterns.


    Moving toward 30 degrees latitude, rainfall becomes seasonally dry,
    and then almost continuously dry. My understanding is, the only
    native forests south of the Caspian are in the mountains, and adjacent
    to the Mediterranean coasts. Arboreal apes of any kind would find
    these deserts impassible.

    You are speaking of recent climate. There are no arboreal apes there now.


    No, I am speaking of climate then *and* now. Regions around 30
    degrees latitude tend to be drier than those around the equator, with exceptions due to terrain and ocean currents.


    To a first approximation, average rainfall and temperature are
    functions of latitude. However, while temperature is a function of
    the sine of latitude, rainfall is more complex. It tends to be
    continuously heavy near the equator, continuously dry near 30 degrees,
    and seasonally variable between 30 and 60 degrees. This general
    pattern is modified, sometimes dramatically, by terrain, ocean
    currents, seasons, and Milankovitch cycles.

    The most significant variable is Africa's northward tectonic
    migration, about a centimeter a year since before the Miocene. So,
    while central Africa has moved from south to north of the equator with
    little effect, north Africa has approached and then went north of 30
    degrees, making it over time ever drier, amplifying other climate
    trends, making once wooded areas into vast savannah and desert.

    Yes.

    Also, Africa's tectonic slide north almost certainly pinched closed
    the Gilbraltar Sttraits, which caused the Mediterranean to dry up at
    least once, and likely several times as sea levels rose and fell. The
    resulting hot salt basin would also have been impassible for arboreal
    apes.
    This is as true now as it was in the
    Miocene. This suggests to me there could not have been an unbroken
    forested path for arboreal apes to migrate between Europe/Near East
    and Central Africa.
    I would not claim nor disclaim that. The Levant is near the midpoint, extends the African Rift valley to Anatolia, is a major avian migration route between Africa and Eurasia, has fossil/artifacts of Homo erectus, neanderthal & sapiens oldest known
    cooking (fish .78ma) and earliest waternut gathering and bread making. The region is amenable to hominins & Homo.
    I acknowledge the facts you describe above. However, the Levant is
    savannah and desert except for a narrow strip along the Mediterranean
    and up in the mountains. While this is no problem for terrestrial
    bipeds like Homo, ISTM arboreal hominids like D.guggenmosi would have
    a much harder time living/migrating there.

    "is".
    Again, refer to microclimate of Levant 11ma - 5ma. Today's Dead Sea was once the vast brackish Lake Lisan that reached to Lebanon, a gallery forest may have reached from Anatolia to Egypt.


    The regions you describe above are part of the Mediterranean coastal
    mountains I mentioned previously. I agree a coastal Mediterranean
    forest is plausible. However, my understanding is the evidence is
    insufficient to say if it would have been as extensive and continuous
    as you suggest during the time you suggest.


    What is ISTM?


    It's shorthand acronym for "It Seems To Me"


    Danuvius, Rudapithecus, Graecopithecus, Oranopithecus each had a unique trait shared with hominins. I think of them as a superspecies with local variations.
    -
    If you place Danuvius half-way between fast brachiating bipedal long backed long achilles tendon hylobatids and bipedal Homo with long back and long achilles tendon, it fits perfectly.

    Wiki:
    Danuvius is thought to have had a broad chest. It is the first recorded Miocene great ape to have had the diaphragm located in the lower chest cavity, as in Homo, indicating an extended lower back and a greater number of functional lumbar vertebrae.
    This may have caused lordosis (the normal curvature of the human spine) and moved the center of mass over the hips and legs, which implies some habitual bipedal activity.

    The robust finger and hypertrophied wrist and elbow bones indicate a strong grip and load bearing adaptations for the arms. The legs also show adaptations for load-bearing, especially at the hypertrophied knee joint. There was likely limited ankle
    loading, and the ankle would have had a hinge-like function, being most stable if positioned perpendicularly to the leg as opposed to at an angle in apes. Danuvius was likely able to achieve a strong grip with its big toes, unlike modern African great
    apes, which would have allowed it to grasp onto thinner trees. The limb proportions are most similar to those of bonobos.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Fri Nov 18 03:45:32 2022
    On Friday, November 18, 2022 at 2:12:32 AM UTC-5, 69jp...@gmail.com wrote:
    On Thu, 17 Nov 2022 15:53:51 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 12:57:57 PM UTC-5, 69jp...@gmail.com wrote:
    On Wed, 16 Nov 2022 22:42:03 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 1:29:04 AM UTC-5, Daud Deden wrote:
    On Wednesday, November 16, 2022 at 11:08:11 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 04 Nov 2022 02:21:55 -0400, jillery <69jp...@gmail.com>
    wrote:

    On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy. >> >> > >>> >
    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a
    Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.


    My impression is there isn't enough evidence to show whether Pliocene
    African apes descended from Miocene European apes or Miocene African
    apes. Either way, there was enough time between the two eras to have
    evolved differences between either Miocene populations and Pliocene S.
    tchadensis.

    I have recently become aware of:

    <https://en.wikipedia.org/wiki/Danuvius_guggenmosi>

    which was a Miocene European ape that may have evolved arboreal
    bipedalism similar to S.tchadensis.

    Depending on how widespread its range, and how successful its
    descendants, it's plausible they lived south of the Black Sea during >> >> > the late Miocene.

    The question then becomes whether it's more likely these apes found >> >> > their way into Africa to become the ancestors of Pliocene
    S.tchadensis, or whether S.tchadensis evolved from Miocene African >> >> > apes.

    Unfortunately, the habitat of these apes made their fossil
    preservation extremely rare, and so the evidence to well support
    either hypothesis is lacking.

    However, the question at least conditionally can be answered by
    comparing the likelihood of a migratory pathway during that time,
    versus the likelihood of arboreal bipedalism evolving independently in
    two populations.

    There are a number of anatomic features associated with arboreal
    bipedalism, some of which are necessary, ex. anterior foramen magnum,

    The foramen magnum is always situated relatively more anteriorly in immature than in mature apes.[ - and men. ]
    Not sure what you mean by "mature"; the individual or the species?

    Individually.
    My understanding is the relative position of foramen magnum doesn't
    change significantly during human development.

    Right. In chimps the muzzle gradually moves anteriorly relative to the foramen magnum, in Homo only the nose does.
    Sorry, I erred above, I'd meant "...than in mature apes." The "and men" was NOT meant, I thought I'd erased it! Oops.

    Either way, the important point is the position and angle of foramen
    magnum are diagnostic among all vertebrates for how they habitually
    hold their head, and so includes/excludes bipedalism among hominids.

    Yes, but no. Great apes are bipedal except when (hurrying) on open ground they adopt quadrupedalism. Homo retains the primitive bipedal gait of hominoid ancestors, as do hylobatids.
    All Homo species are great apes by definition, including H.sapiens.

    Yes, I meant 'arboreal great apes'. Humans are terrestrial great apes, hylobatids are arboreal lesser apes.

    They do/did quadrupedalism only in exceptional cases.

    https://youtu.be/pCrH6BOwxe4 15mph qpal running as a patas monkey, not a chimp.

    and some of which are incidental, ex. molar patterns. Descendant
    populations are more likely to share these features than are
    independent populations. This suggests to me that a sufficiently
    robust fossil record could answer this question with some degree of >> >> > certainty.

    Alternately, my understanding is southern Europe and central Africa >> >> > are ecological opposites, in the sense that when one is hot and dry >> >> > the other is temperate and wet.
    Central Africa is and was hot,
    ... and wet aka tropical,

    The adoption of qpal knucklewalking by African apes indicates that their ancient habitat went through a dry phase (rainforest became patchy) forcing a terrestrial dog-like gait.
    Perhaps. My understanding is bipedal arboreal apes continued to walk bipedally on the ground, while non-bipedal arboreal apes also adopted quadrupedal habits on the ground.

    Bipedal walking is primitive in arboreal hominoids, quadrupedal walking is derived. I don't know of any 'non-bipedal arboreal apes', only monkeys.

    just right for the evolution of small bipedal arboreal apes.

    The fact that there are no small bipedal arboreal apes in Africa indicates that there was some climate shifting.
    Again perhaps. It also suggests small bipedal arboreal apes were outcompeted.

    They were, by monkeys which were more ground adapted, able to swiftly run between forest stands during a drier climate phase.

    the southern Black Sea is between temperate and tropical.
    Correct. Southern Europe and the Black Sea are at the same latitudes.
    This suggests they would tend to have the same climate. However, the
    Black Sea is farther inland, and so suffers more continental extremes.
    So any climate changes will appear first around the Black Sea and
    become more extreme compared to southern Europe.

    I'm talking about from 11ma through the MSC to 5ma. The Medit. & Red Seas dried out, the Black Sea didn't.
    The relative position of the Black Sea didn't change from then to now.
    The important point is its position is deep in Eurasia, where
    continental climates rule.

    It lies between the Atlantic-Mediterranean and the Caspian Sea, in the Peri-Tethyan basin, protected by the high Iranian plateau to the south. Not a typical continental climate.

    My understanding is the Mediterranean dried out only about 6mya, long
    after European, and presumably Black Sea, arboreal apes went extinct.

    No, Danuvius and later Miocene apes there were of one lineage IMO, that may have lived there until 5ma, with successive expansional waves emigrating outwardly including towards Africa.

    The Red Sea is too far south to affect migration from Europe to Africa regardless of climate patterns.

    It is part of the African-Anatolian rift.

    Moving toward 30 degrees latitude, rainfall becomes seasonally dry,
    and then almost continuously dry. My understanding is, the only
    native forests south of the Caspian are in the mountains, and adjacent
    to the Mediterranean coasts. Arboreal apes of any kind would find
    these deserts impassible.

    You are speaking of recent climate. There are no arboreal apes there now. No, I am speaking of climate then *and* now. Regions around 30
    degrees latitude tend to be drier than those around the equator, with exceptions due to terrain and ocean currents.

    You appear to be claiming that the European Miocene apes could never have been linked to African and Asian apes. Yet they certainly were, else they wouldn't have existed at all.

    To a first approximation, average rainfall and temperature are
    functions of latitude. However, while temperature is a function of
    the sine of latitude, rainfall is more complex. It tends to be
    continuously heavy near the equator, continuously dry near 30 degrees,
    and seasonally variable between 30 and 60 degrees. This general
    pattern is modified, sometimes dramatically, by terrain, ocean
    currents, seasons, and Milankovitch cycles.

    The most significant variable is Africa's northward tectonic
    migration, about a centimeter a year since before the Miocene. So,
    while central Africa has moved from south to north of the equator with
    little effect, north Africa has approached and then went north of 30
    degrees, making it over time ever drier, amplifying other climate
    trends, making once wooded areas into vast savannah and desert.

    Yes.

    Also, Africa's tectonic slide north almost certainly pinched closed
    the Gilbraltar Sttraits, which caused the Mediterranean to dry up at
    least once, and likely several times as sea levels rose and fell. The
    resulting hot salt basin would also have been impassible for arboreal
    apes.
    This is as true now as it was in the
    Miocene. This suggests to me there could not have been an unbroken >> >> > forested path for arboreal apes to migrate between Europe/Near East >> >> > and Central Africa.
    I would not claim nor disclaim that. The Levant is near the midpoint, extends the African Rift valley to Anatolia, is a major avian migration route between Africa and Eurasia, has fossil/artifacts of Homo erectus, neanderthal & sapiens oldest
    known cooking (fish .78ma) and earliest waternut gathering and bread making. The region is amenable to hominins & Homo.
    I acknowledge the facts you describe above. However, the Levant is
    savannah and desert except for a narrow strip along the Mediterranean
    and up in the mountains. While this is no problem for terrestrial
    bipeds like Homo, ISTM arboreal hominids like D.guggenmosi would have
    a much harder time living/migrating there.

    "is".
    Again, refer to microclimate of Levant 11ma - 5ma. Today's Dead Sea was once the vast brackish Lake Lisan that reached to Lebanon, a gallery forest may have reached from Anatolia to Egypt.
    The regions you describe above are part of the Mediterranean coastal mountains I mentioned previously.

    The Dead Sea is by no means a coastal mountain region.

    I agree a coastal Mediterranean
    forest is plausible.

    I'm referring to the tectonic rift valley between Zimbabwe/Zambia and Lebanon/Anatolia.
    Of course, there were coastal forests as well, but they were affected by the MSC.

    However, my understanding is the evidence is
    insufficient to say if it would have been as extensive and continuous
    as you suggest during the time you suggest.

    Haven't got enough hard data yet.

    What is ISTM?


    It's shorthand acronym for "It Seems To Me"

    Ok, thanks.

    Danuvius, Rudapithecus, Graecopithecus, Oranopithecus each had a unique trait shared with hominins. I think of them as a superspecies with local variations.
    -
    If you place Danuvius half-way between fast brachiating bipedal long backed long achilles tendon hylobatids and bipedal Homo with long back and long achilles tendon, it fits perfectly.

    Wiki:
    Danuvius is thought to have had a broad chest. It is the first recorded Miocene great ape to have had the diaphragm located in the lower chest cavity, as in Homo, indicating an extended lower back and a greater number of functional lumbar vertebrae.
    This may have caused lordosis (the normal curvature of the human spine) and moved the center of mass over the hips and legs, which implies some habitual bipedal activity.

    The robust finger and hypertrophied wrist and elbow bones indicate a strong grip and load bearing adaptations for the arms. The legs also show adaptations for load-bearing, especially at the hypertrophied knee joint. There was likely limited ankle
    loading, and the ankle would have had a hinge-like function, being most stable if positioned perpendicularly to the leg as opposed to at an angle in apes. Danuvius was likely able to achieve a strong grip with its big toes, unlike modern African great
    apes, which would have allowed it to grasp onto thinner trees. The limb proportions are most similar to those of bonobos.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to Daud Deden on Fri Nov 18 04:55:36 2022
    On Friday, November 18, 2022 at 6:45:33 AM UTC-5, Daud Deden wrote:
    On Friday, November 18, 2022 at 2:12:32 AM UTC-5, 69jp...@gmail.com wrote:
    On Thu, 17 Nov 2022 15:53:51 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 12:57:57 PM UTC-5, 69jp...@gmail.com wrote:
    On Wed, 16 Nov 2022 22:42:03 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 1:29:04 AM UTC-5, Daud Deden wrote: >> >> On Wednesday, November 16, 2022 at 11:08:11 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 04 Nov 2022 02:21:55 -0400, jillery <69jp...@gmail.com>
    wrote:

    On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism. >> >> > >>> >> >>
    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a
    Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.


    My impression is there isn't enough evidence to show whether Pliocene
    African apes descended from Miocene European apes or Miocene African
    apes. Either way, there was enough time between the two eras to have
    evolved differences between either Miocene populations and Pliocene S.
    tchadensis.

    I have recently become aware of:

    <https://en.wikipedia.org/wiki/Danuvius_guggenmosi>

    which was a Miocene European ape that may have evolved arboreal
    bipedalism similar to S.tchadensis.

    Depending on how widespread its range, and how successful its
    descendants, it's plausible they lived south of the Black Sea during
    the late Miocene.

    The question then becomes whether it's more likely these apes found
    their way into Africa to become the ancestors of Pliocene
    S.tchadensis, or whether S.tchadensis evolved from Miocene African >> >> > apes.

    Unfortunately, the habitat of these apes made their fossil
    preservation extremely rare, and so the evidence to well support >> >> > either hypothesis is lacking.

    However, the question at least conditionally can be answered by
    comparing the likelihood of a migratory pathway during that time, >> >> > versus the likelihood of arboreal bipedalism evolving independently in
    two populations.

    There are a number of anatomic features associated with arboreal >> >> > bipedalism, some of which are necessary, ex. anterior foramen magnum,

    The foramen magnum is always situated relatively more anteriorly in immature than in mature apes.[ - and men. ]
    Not sure what you mean by "mature"; the individual or the species?

    Individually.
    My understanding is the relative position of foramen magnum doesn't
    change significantly during human development.
    Right. In chimps the muzzle gradually moves anteriorly relative to the foramen magnum, in Homo only the nose does.
    Sorry, I erred above, I'd meant "...than in mature apes." The "and men" was NOT meant, I thought I'd erased it! Oops.
    Either way, the important point is the position and angle of foramen
    magnum are diagnostic among all vertebrates for how they habitually
    hold their head, and so includes/excludes bipedalism among hominids.

    Yes, but no. Great apes are bipedal except when (hurrying) on open ground they adopt quadrupedalism. Homo retains the primitive bipedal gait of hominoid ancestors, as do hylobatids.
    All Homo species are great apes by definition, including H.sapiens.
    Yes, I meant 'arboreal great apes'. Humans are terrestrial great apes, hylobatids are arboreal lesser apes.
    They do/did quadrupedalism only in exceptional cases.
    https://youtu.be/pCrH6BOwxe4 15mph qpal running as a patas monkey, not a chimp.
    and some of which are incidental, ex. molar patterns. Descendant >> >> > populations are more likely to share these features than are
    independent populations. This suggests to me that a sufficiently >> >> > robust fossil record could answer this question with some degree of
    certainty.

    Alternately, my understanding is southern Europe and central Africa
    are ecological opposites, in the sense that when one is hot and dry
    the other is temperate and wet.
    Central Africa is and was hot,
    ... and wet aka tropical,

    The adoption of qpal knucklewalking by African apes indicates that their ancient habitat went through a dry phase (rainforest became patchy) forcing a terrestrial dog-like gait.
    Perhaps. My understanding is bipedal arboreal apes continued to walk bipedally on the ground, while non-bipedal arboreal apes also adopted quadrupedal habits on the ground.
    Bipedal walking is primitive in arboreal hominoids, quadrupedal walking is derived. I don't know of any 'non-bipedal arboreal apes', only monkeys.
    just right for the evolution of small bipedal arboreal apes.

    The fact that there are no small bipedal arboreal apes in Africa indicates that there was some climate shifting.
    Again perhaps. It also suggests small bipedal arboreal apes were outcompeted.
    They were, by monkeys which were more ground adapted, able to swiftly run between forest stands during a drier climate phase.
    the southern Black Sea is between temperate and tropical.
    Correct. Southern Europe and the Black Sea are at the same latitudes. >> This suggests they would tend to have the same climate. However, the
    Black Sea is farther inland, and so suffers more continental extremes. >> So any climate changes will appear first around the Black Sea and
    become more extreme compared to southern Europe.

    I'm talking about from 11ma through the MSC to 5ma. The Medit. & Red Seas dried out, the Black Sea didn't.
    The relative position of the Black Sea didn't change from then to now.
    The important point is its position is deep in Eurasia, where
    continental climates rule.
    It lies between the Atlantic-Mediterranean and the Caspian Sea, in the Peri-Tethyan basin, protected by the high Iranian plateau to the south. Not a typical continental climate.
    My understanding is the Mediterranean dried out only about 6mya, long after European, and presumably Black Sea, arboreal apes went extinct.
    No, Danuvius and later Miocene apes there were of one lineage IMO, that may have lived there until 5ma, with successive expansional waves emigrating outwardly including towards Africa.
    The Red Sea is too far south to affect migration from Europe to Africa regardless of climate patterns.
    It is part of the African-Anatolian rift.
    Moving toward 30 degrees latitude, rainfall becomes seasonally dry,
    and then almost continuously dry. My understanding is, the only
    native forests south of the Caspian are in the mountains, and adjacent >> to the Mediterranean coasts. Arboreal apes of any kind would find
    these deserts impassible.

    You are speaking of recent climate. There are no arboreal apes there now. No, I am speaking of climate then *and* now. Regions around 30
    degrees latitude tend to be drier than those around the equator, with exceptions due to terrain and ocean currents.
    You appear to be claiming that the European Miocene apes could never have been linked to African and Asian apes. Yet they certainly were, else they wouldn't have existed at all.
    To a first approximation, average rainfall and temperature are
    functions of latitude. However, while temperature is a function of
    the sine of latitude, rainfall is more complex. It tends to be
    continuously heavy near the equator, continuously dry near 30 degrees, >> and seasonally variable between 30 and 60 degrees. This general
    pattern is modified, sometimes dramatically, by terrain, ocean
    currents, seasons, and Milankovitch cycles.

    The most significant variable is Africa's northward tectonic
    migration, about a centimeter a year since before the Miocene. So,
    while central Africa has moved from south to north of the equator with >> little effect, north Africa has approached and then went north of 30
    degrees, making it over time ever drier, amplifying other climate
    trends, making once wooded areas into vast savannah and desert.

    Yes.

    Also, Africa's tectonic slide north almost certainly pinched closed
    the Gilbraltar Sttraits, which caused the Mediterranean to dry up at
    least once, and likely several times as sea levels rose and fell. The >> resulting hot salt basin would also have been impassible for arboreal >> apes.
    This is as true now as it was in the
    Miocene. This suggests to me there could not have been an unbroken >> >> > forested path for arboreal apes to migrate between Europe/Near East
    and Central Africa.
    I would not claim nor disclaim that. The Levant is near the midpoint, extends the African Rift valley to Anatolia, is a major avian migration route between Africa and Eurasia, has fossil/artifacts of Homo erectus, neanderthal & sapiens oldest
    known cooking (fish .78ma) and earliest waternut gathering and bread making. The region is amenable to hominins & Homo.
    I acknowledge the facts you describe above. However, the Levant is
    savannah and desert except for a narrow strip along the Mediterranean >> and up in the mountains. While this is no problem for terrestrial
    bipeds like Homo, ISTM arboreal hominids like D.guggenmosi would have >> a much harder time living/migrating there.

    "is".
    Again, refer to microclimate of Levant 11ma - 5ma. Today's Dead Sea was once the vast brackish Lake Lisan that reached to Lebanon, a gallery forest may have reached from Anatolia to Egypt.
    The regions you describe above are part of the Mediterranean coastal mountains I mentioned previously.
    The Dead Sea is by no means a coastal mountain region.
    I agree a coastal Mediterranean
    forest is plausible.
    I'm referring to the tectonic rift valley between Zimbabwe/Zambia and Lebanon/Anatolia.
    Of course, there were coastal forests as well, but they were affected by the MSC.
    However, my understanding is the evidence is
    insufficient to say if it would have been as extensive and continuous
    as you suggest during the time you suggest.
    Haven't got enough hard data yet.
    What is ISTM?


    It's shorthand acronym for "It Seems To Me"
    Ok, thanks.
    Danuvius, Rudapithecus, Graecopithecus, Oranopithecus each had a unique trait shared with hominins. I think of them as a superspecies with local variations.
    -
    If you place Danuvius half-way between fast brachiating bipedal long backed long achilles tendon hylobatids and bipedal Homo with long back and long achilles tendon, it fits perfectly.

    Wiki:
    Danuvius is thought to have had a broad chest. It is the first recorded Miocene great ape to have had the diaphragm located in the lower chest cavity, as in Homo, indicating an extended lower back and a greater number of functional lumbar
    vertebrae. This may have caused lordosis (the normal curvature of the human spine) and moved the center of mass over the hips and legs, which implies some habitual bipedal activity.

    The robust finger and hypertrophied wrist and elbow bones indicate a strong grip and load bearing adaptations for the arms. The legs also show adaptations for load-bearing, especially at the hypertrophied knee joint. There was likely limited
    ankle loading, and the ankle would have had a hinge-like function, being most stable if positioned perpendicularly to the leg as opposed to at an angle in apes. Danuvius was likely able to achieve a strong grip with its big toes, unlike modern African
    great apes, which would have allowed it to grasp onto thinner trees. The limb proportions are most similar to those of bonobos.

    OT, h/t Pandora at SAP, diving whale at Turkana 17ma, before tectonic uplifting & aridification: https://www.pnas.org/doi/10.1073/pnas.1421502112
    Also later, stingray.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to daud.deden@gmail.com on Sat Nov 19 06:39:57 2022
    On Fri, 18 Nov 2022 03:45:32 -0800 (PST), Daud Deden
    <daud.deden@gmail.com> wrote:

    On Friday, November 18, 2022 at 2:12:32 AM UTC-5, 69jp...@gmail.com wrote:
    On Thu, 17 Nov 2022 15:53:51 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 12:57:57 PM UTC-5, 69jp...@gmail.com wrote:
    On Wed, 16 Nov 2022 22:42:03 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 1:29:04 AM UTC-5, Daud Deden wrote: >> >> >> On Wednesday, November 16, 2022 at 11:08:11 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 04 Nov 2022 02:21:55 -0400, jillery <69jp...@gmail.com>
    wrote:

    On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a
    Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.


    My impression is there isn't enough evidence to show whether Pliocene
    African apes descended from Miocene European apes or Miocene African
    apes. Either way, there was enough time between the two eras to have
    evolved differences between either Miocene populations and Pliocene S.
    tchadensis.

    I have recently become aware of:

    <https://en.wikipedia.org/wiki/Danuvius_guggenmosi>

    which was a Miocene European ape that may have evolved arboreal
    bipedalism similar to S.tchadensis.

    Depending on how widespread its range, and how successful its
    descendants, it's plausible they lived south of the Black Sea during
    the late Miocene.

    The question then becomes whether it's more likely these apes found >> >> >> > their way into Africa to become the ancestors of Pliocene
    S.tchadensis, or whether S.tchadensis evolved from Miocene African >> >> >> > apes.

    Unfortunately, the habitat of these apes made their fossil
    preservation extremely rare, and so the evidence to well support
    either hypothesis is lacking.

    However, the question at least conditionally can be answered by
    comparing the likelihood of a migratory pathway during that time, >> >> >> > versus the likelihood of arboreal bipedalism evolving independently in
    two populations.

    There are a number of anatomic features associated with arboreal
    bipedalism, some of which are necessary, ex. anterior foramen magnum,

    The foramen magnum is always situated relatively more anteriorly in immature than in mature apes.[ - and men. ]
    Not sure what you mean by "mature"; the individual or the species?

    Individually.
    My understanding is the relative position of foramen magnum doesn't
    change significantly during human development.

    Right. In chimps the muzzle gradually moves anteriorly relative to the foramen magnum, in Homo only the nose does.
    Sorry, I erred above, I'd meant "...than in mature apes." The "and men" was NOT meant, I thought I'd erased it! Oops.


    The positions of the muzzle and/or nose relative to the foramen magnum
    don't inform bipedalism.


    Either way, the important point is the position and angle of foramen
    magnum are diagnostic among all vertebrates for how they habitually
    hold their head, and so includes/excludes bipedalism among hominids.

    Yes, but no. Great apes are bipedal except when (hurrying) on open ground they adopt quadrupedalism. Homo retains the primitive bipedal gait of hominoid ancestors, as do hylobatids.
    All Homo species are great apes by definition, including H.sapiens.

    Yes, I meant 'arboreal great apes'. Humans are terrestrial great apes, hylobatids are arboreal lesser apes.

    They do/did quadrupedalism only in exceptional cases.

    https://youtu.be/pCrH6BOwxe4 15mph qpal running as a patas monkey, not a chimp.


    Imagine how much faster that person would be if he ran normally, like
    this:

    <https://www.youtube.com/watch?v=k3PZgbQ8auE>


    and some of which are incidental, ex. molar patterns. Descendant
    populations are more likely to share these features than are
    independent populations. This suggests to me that a sufficiently
    robust fossil record could answer this question with some degree of >> >> >> > certainty.

    Alternately, my understanding is southern Europe and central Africa >> >> >> > are ecological opposites, in the sense that when one is hot and dry >> >> >> > the other is temperate and wet.
    Central Africa is and was hot,
    ... and wet aka tropical,

    The adoption of qpal knucklewalking by African apes indicates that their ancient habitat went through a dry phase (rainforest became patchy) forcing a terrestrial dog-like gait.
    Perhaps. My understanding is bipedal arboreal apes continued to walk
    bipedally on the ground, while non-bipedal arboreal apes also adopted
    quadrupedal habits on the ground.

    Bipedal walking is primitive in arboreal hominoids, quadrupedal walking is derived. I don't know of any 'non-bipedal arboreal apes', only monkeys.


    That's not my understanding. My understanding is chimpanzees,
    gorillas, and orangutans are non-bipedal arboreal apes, meaning when
    they are in the trees, they do not walk upright. As were most
    arboreal apes prior to Australopithecines.


    just right for the evolution of small bipedal arboreal apes.

    The fact that there are no small bipedal arboreal apes in Africa indicates that there was some climate shifting.
    Again perhaps. It also suggests small bipedal arboreal apes were
    outcompeted.

    They were, by monkeys which were more ground adapted, able to swiftly run between forest stands during a drier climate phase.

    the southern Black Sea is between temperate and tropical.
    Correct. Southern Europe and the Black Sea are at the same latitudes.
    This suggests they would tend to have the same climate. However, the
    Black Sea is farther inland, and so suffers more continental extremes. >> >> So any climate changes will appear first around the Black Sea and
    become more extreme compared to southern Europe.

    I'm talking about from 11ma through the MSC to 5ma. The Medit. & Red Seas dried out, the Black Sea didn't.
    The relative position of the Black Sea didn't change from then to now.
    The important point is its position is deep in Eurasia, where
    continental climates rule.

    It lies between the Atlantic-Mediterranean and the Caspian Sea, in the Peri-Tethyan basin, protected by the high Iranian plateau to the south. Not a typical continental climate.


    <https://www.britannica.com/place/Black-Sea/Climate> **********************************
    The climate of the landlocked Black Sea can be characterized generally
    as continental (i.e., subject to pronounced seasonal temperature
    variations), although climatic conditions in some parts of the basin
    are controlled to a great extent by the shoreline relief. A steppe
    climate, with cold winters and hot, dry summers, is found in the
    northwestern part of the basin exposed to the influence of air masses
    from the north.
    ************************************


    My understanding is the Mediterranean dried out only about 6mya, long
    after European, and presumably Black Sea, arboreal apes went extinct.

    No, Danuvius and later Miocene apes there were of one lineage IMO, that may have lived there until 5ma, with successive expansional waves emigrating outwardly including towards Africa.

    The Red Sea is too far south to affect migration from Europe to Africa
    regardless of climate patterns.

    It is part of the African-Anatolian rift.


    I acknowledge that rift was one plausible pathway from Europe to
    Africa. The Red Sea was not, nor did it block such a pathway.


    Moving toward 30 degrees latitude, rainfall becomes seasonally dry,
    and then almost continuously dry. My understanding is, the only
    native forests south of the Caspian are in the mountains, and adjacent >> >> to the Mediterranean coasts. Arboreal apes of any kind would find
    these deserts impassible.

    You are speaking of recent climate. There are no arboreal apes there now. >> No, I am speaking of climate then *and* now. Regions around 30
    degrees latitude tend to be drier than those around the equator, with
    exceptions due to terrain and ocean currents.

    You appear to be claiming that the European Miocene apes could never have been linked to African and Asian apes. Yet they certainly were, else they wouldn't have existed at all.


    Such an "appearance" is incorrect. In certain cases, regions around
    30 degrees latitude have/had enough rainfall to support forests. The
    relevant point here is, global climate since the Miocene has gotten
    colder and drier, especially around 30 degrees latitude, which has led
    to the creation of large areas of treeless savannah and desert. I
    don't know when European and African forests separated. Do you?

    Also, the question isn't about the origin of apes generally. It's
    about the origin of arboreal bipedal apes. We know they existed in
    Pliocene Africa. They *may* have existed in Miocene Europe. Even if
    they did, the two populations may still have evolved independently.


    To a first approximation, average rainfall and temperature are
    functions of latitude. However, while temperature is a function of
    the sine of latitude, rainfall is more complex. It tends to be
    continuously heavy near the equator, continuously dry near 30 degrees, >> >> and seasonally variable between 30 and 60 degrees. This general
    pattern is modified, sometimes dramatically, by terrain, ocean
    currents, seasons, and Milankovitch cycles.

    The most significant variable is Africa's northward tectonic
    migration, about a centimeter a year since before the Miocene. So,
    while central Africa has moved from south to north of the equator with >> >> little effect, north Africa has approached and then went north of 30
    degrees, making it over time ever drier, amplifying other climate
    trends, making once wooded areas into vast savannah and desert.

    Yes.

    Also, Africa's tectonic slide north almost certainly pinched closed
    the Gilbraltar Sttraits, which caused the Mediterranean to dry up at
    least once, and likely several times as sea levels rose and fell. The
    resulting hot salt basin would also have been impassible for arboreal
    apes.
    This is as true now as it was in the
    Miocene. This suggests to me there could not have been an unbroken >> >> >> > forested path for arboreal apes to migrate between Europe/Near East >> >> >> > and Central Africa.
    I would not claim nor disclaim that. The Levant is near the midpoint, extends the African Rift valley to Anatolia, is a major avian migration route between Africa and Eurasia, has fossil/artifacts of Homo erectus, neanderthal & sapiens oldest
    known cooking (fish .78ma) and earliest waternut gathering and bread making. The region is amenable to hominins & Homo.
    I acknowledge the facts you describe above. However, the Levant is
    savannah and desert except for a narrow strip along the Mediterranean
    and up in the mountains. While this is no problem for terrestrial
    bipeds like Homo, ISTM arboreal hominids like D.guggenmosi would have
    a much harder time living/migrating there.

    "is".
    Again, refer to microclimate of Levant 11ma - 5ma. Today's Dead Sea was once the vast brackish Lake Lisan that reached to Lebanon, a gallery forest may have reached from Anatolia to Egypt.
    The regions you describe above are part of the Mediterranean coastal
    mountains I mentioned previously.

    The Dead Sea is by no means a coastal mountain region.


    https://en.wikipedia.org/wiki/Judaean_Mountains

    These are part of a series of ranges all along the eastern
    Mediterranean coast.


    I agree a coastal Mediterranean
    forest is plausible.

    I'm referring to the tectonic rift valley between Zimbabwe/Zambia and Lebanon/Anatolia.


    ... which runs parallel to the Mediterranean coast.


    Of course, there were coastal forests as well, but they were affected by the MSC.

    However, my understanding is the evidence is
    insufficient to say if it would have been as extensive and continuous
    as you suggest during the time you suggest.

    Haven't got enough hard data yet.


    Cite the data you think is sufficient to answer this question.


    What is ISTM?


    It's shorthand acronym for "It Seems To Me"

    Ok, thanks.

    Danuvius, Rudapithecus, Graecopithecus, Oranopithecus each had a unique trait shared with hominins. I think of them as a superspecies with local variations.
    -
    If you place Danuvius half-way between fast brachiating bipedal long backed long achilles tendon hylobatids and bipedal Homo with long back and long achilles tendon, it fits perfectly.

    Wiki:
    Danuvius is thought to have had a broad chest. It is the first recorded Miocene great ape to have had the diaphragm located in the lower chest cavity, as in Homo, indicating an extended lower back and a greater number of functional lumbar
    vertebrae. This may have caused lordosis (the normal curvature of the human spine) and moved the center of mass over the hips and legs, which implies some habitual bipedal activity.

    The robust finger and hypertrophied wrist and elbow bones indicate a strong grip and load bearing adaptations for the arms. The legs also show adaptations for load-bearing, especially at the hypertrophied knee joint. There was likely limited ankle
    loading, and the ankle would have had a hinge-like function, being most stable if positioned perpendicularly to the leg as opposed to at an angle in apes. Danuvius was likely able to achieve a strong grip with its big toes, unlike modern African great
    apes, which would have allowed it to grasp onto thinner trees. The limb proportions are most similar to those of bonobos.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Sat Nov 19 06:06:22 2022
    On Saturday, November 19, 2022 at 6:40:01 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 18 Nov 2022 03:45:32 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, November 18, 2022 at 2:12:32 AM UTC-5, 69jp...@gmail.com wrote: >> On Thu, 17 Nov 2022 15:53:51 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 12:57:57 PM UTC-5, 69jp...@gmail.com wrote:
    On Wed, 16 Nov 2022 22:42:03 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 1:29:04 AM UTC-5, Daud Deden wrote: >> >> >> On Wednesday, November 16, 2022 at 11:08:11 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 04 Nov 2022 02:21:55 -0400, jillery <69jp...@gmail.com> >> >> >> > wrote:

    On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism. >> >> >> > >>> >> >>
    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a
    Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.


    My impression is there isn't enough evidence to show whether Pliocene
    African apes descended from Miocene European apes or Miocene African
    apes. Either way, there was enough time between the two eras to have
    evolved differences between either Miocene populations and Pliocene S.
    tchadensis.

    I have recently become aware of:

    <https://en.wikipedia.org/wiki/Danuvius_guggenmosi>

    which was a Miocene European ape that may have evolved arboreal >> >> >> > bipedalism similar to S.tchadensis.

    Depending on how widespread its range, and how successful its
    descendants, it's plausible they lived south of the Black Sea during
    the late Miocene.

    The question then becomes whether it's more likely these apes found
    their way into Africa to become the ancestors of Pliocene
    S.tchadensis, or whether S.tchadensis evolved from Miocene African
    apes.

    Unfortunately, the habitat of these apes made their fossil
    preservation extremely rare, and so the evidence to well support >> >> >> > either hypothesis is lacking.

    However, the question at least conditionally can be answered by >> >> >> > comparing the likelihood of a migratory pathway during that time, >> >> >> > versus the likelihood of arboreal bipedalism evolving independently in
    two populations.

    There are a number of anatomic features associated with arboreal >> >> >> > bipedalism, some of which are necessary, ex. anterior foramen magnum,

    The foramen magnum is always situated relatively more anteriorly in immature than in mature apes.[ - and men. ]
    Not sure what you mean by "mature"; the individual or the species?

    Individually.
    My understanding is the relative position of foramen magnum doesn't
    change significantly during human development.

    Right. In chimps the muzzle gradually moves anteriorly relative to the foramen magnum, in Homo only the nose does.
    Sorry, I erred above, I'd meant "...than in mature apes." The "and men" was NOT meant, I thought I'd erased it! Oops.
    The positions of the muzzle and/or nose relative to the foramen magnum
    don't inform bipedalism.

    It does, in tail-less upright orthogonal striding terrestrial former/partial arboreal bipeds, it does not in hopping bipeds.
    Cf short-faced giant kangaroo (short tail, striding upright bipedal)

    Either way, the important point is the position and angle of foramen >> >> magnum are diagnostic among all vertebrates for how they habitually
    hold their head, and so includes/excludes bipedalism among hominids. >> >
    Yes, but no. Great apes are bipedal except when (hurrying) on open ground they adopt quadrupedalism. Homo retains the primitive bipedal gait of hominoid ancestors, as do hylobatids.
    All Homo species are great apes by definition, including H.sapiens.

    Yes, I meant 'arboreal great apes'. Humans are terrestrial great apes, hylobatids are arboreal lesser apes.

    They do/did quadrupedalism only in exceptional cases.

    https://youtu.be/pCrH6BOwxe4 15mph qpal running as a patas monkey, not a chimp.
    Imagine how much faster that person would be if he ran normally, like
    this:

    <https://www.youtube.com/watch?v=k3PZgbQ8auE>
    How is that an exceptional case among hominins? Only Usain Bolt can outrun qpal chimp at top speed.

    and some of which are incidental, ex. molar patterns. Descendant >> >> >> > populations are more likely to share these features than are
    independent populations. This suggests to me that a sufficiently >> >> >> > robust fossil record could answer this question with some degree of
    certainty.

    Alternately, my understanding is southern Europe and central Africa
    are ecological opposites, in the sense that when one is hot and dry
    the other is temperate and wet.
    Central Africa is and was hot,
    ... and wet aka tropical,

    The adoption of qpal knucklewalking by African apes indicates that their ancient habitat went through a dry phase (rainforest became patchy) forcing a terrestrial dog-like gait.
    Perhaps. My understanding is bipedal arboreal apes continued to walk
    bipedally on the ground, while non-bipedal arboreal apes also adopted
    quadrupedal habits on the ground.

    Bipedal walking is primitive in arboreal hominoids, quadrupedal walking is derived. I don't know of any 'non-bipedal arboreal apes', only monkeys.
    That's not my understanding. My understanding is chimpanzees,
    gorillas, and orangutans are non-bipedal arboreal apes, meaning when
    they are in the trees, they do not walk upright.

    Their body orientation on and under branches is primarily upright, not pronograde with all limbs in compression aka quadrupedal. The modern AMHs orthogonal posture is derived, not the same as primitive upright bipedal arboreal hominoids.

    As were most
    arboreal apes prior to Australopithecines.
    just right for the evolution of small bipedal arboreal apes.

    The fact that there are no small bipedal arboreal apes in Africa indicates that there was some climate shifting.
    Again perhaps. It also suggests small bipedal arboreal apes were
    outcompeted.

    They were, by monkeys which were more ground adapted, able to swiftly run between forest stands during a drier climate phase.

    the southern Black Sea is between temperate and tropical.
    Correct. Southern Europe and the Black Sea are at the same latitudes. >> >> This suggests they would tend to have the same climate. However, the >> >> Black Sea is farther inland, and so suffers more continental extremes. >> >> So any climate changes will appear first around the Black Sea and
    become more extreme compared to southern Europe.

    I'm talking about from 11ma through the MSC to 5ma. The Medit. & Red Seas dried out, the Black Sea didn't.
    The relative position of the Black Sea didn't change from then to now.
    The important point is its position is deep in Eurasia, where
    continental climates rule.

    It lies between the Atlantic-Mediterranean and the Caspian Sea, in the Peri-Tethyan basin, protected by the high Iranian plateau to the south. Not a typical continental climate.
    <https://www.britannica.com/place/Black-Sea/Climate> **********************************
    The climate of the landlocked Black Sea can be characterized generally
    as continental (i.e., subject to pronounced seasonal temperature variations), although climatic conditions in some parts of the basin
    are controlled to a great extent by the shoreline relief. A steppe
    climate, with cold winters and hot, dry summers, is found in the northwestern part of the basin exposed to the influence of air masses
    from the north.
    ************************************

    Summer in north including Bavaria via Danube valley, winter in south including visits further southwardly.

    My understanding is the Mediterranean dried out only about 6mya, long
    after European, and presumably Black Sea, arboreal apes went extinct.

    No, Danuvius and later Miocene apes there were of one lineage IMO, that may have lived there until 5ma, with successive expansional waves emigrating outwardly including towards Africa.

    The Red Sea is too far south to affect migration from Europe to Africa
    regardless of climate patterns.

    It is part of the African-Anatolian rift.
    I acknowledge that rift was one plausible pathway from Europe to
    Africa. The Red Sea was not, nor did it block such a pathway.

    I include it provisionally, more data needed.

    Moving toward 30 degrees latitude, rainfall becomes seasonally dry,
    and then almost continuously dry. My understanding is, the only
    native forests south of the Caspian are in the mountains, and adjacent >> >> to the Mediterranean coasts. Arboreal apes of any kind would find
    these deserts impassible.

    You are speaking of recent climate. There are no arboreal apes there now.
    No, I am speaking of climate then *and* now. Regions around 30
    degrees latitude tend to be drier than those around the equator, with
    exceptions due to terrain and ocean currents.

    Stop temporarily.


    You appear to be claiming that the European Miocene apes could never have been linked to African and Asian apes. Yet they certainly were, else they wouldn't have existed at all.
    Such an "appearance" is incorrect. In certain cases, regions around
    30 degrees latitude have/had enough rainfall to support forests. The relevant point here is, global climate since the Miocene has gotten
    colder and drier, especially around 30 degrees latitude, which has led
    to the creation of large areas of treeless savannah and desert. I
    don't know when European and African forests separated. Do you?

    Also, the question isn't about the origin of apes generally. It's
    about the origin of arboreal bipedal apes. We know they existed in
    Pliocene Africa. They *may* have existed in Miocene Europe. Even if
    they did, the two populations may still have evolved independently.
    To a first approximation, average rainfall and temperature are
    functions of latitude. However, while temperature is a function of
    the sine of latitude, rainfall is more complex. It tends to be
    continuously heavy near the equator, continuously dry near 30 degrees, >> >> and seasonally variable between 30 and 60 degrees. This general
    pattern is modified, sometimes dramatically, by terrain, ocean
    currents, seasons, and Milankovitch cycles.

    The most significant variable is Africa's northward tectonic
    migration, about a centimeter a year since before the Miocene. So,
    while central Africa has moved from south to north of the equator with >> >> little effect, north Africa has approached and then went north of 30 >> >> degrees, making it over time ever drier, amplifying other climate
    trends, making once wooded areas into vast savannah and desert.

    Yes.

    Also, Africa's tectonic slide north almost certainly pinched closed
    the Gilbraltar Sttraits, which caused the Mediterranean to dry up at >> >> least once, and likely several times as sea levels rose and fell. The >> >> resulting hot salt basin would also have been impassible for arboreal >> >> apes.
    This is as true now as it was in the
    Miocene. This suggests to me there could not have been an unbroken
    forested path for arboreal apes to migrate between Europe/Near East
    and Central Africa.
    I would not claim nor disclaim that. The Levant is near the midpoint, extends the African Rift valley to Anatolia, is a major avian migration route between Africa and Eurasia, has fossil/artifacts of Homo erectus, neanderthal & sapiens oldest
    known cooking (fish .78ma) and earliest waternut gathering and bread making. The region is amenable to hominins & Homo.
    I acknowledge the facts you describe above. However, the Levant is
    savannah and desert except for a narrow strip along the Mediterranean >> >> and up in the mountains. While this is no problem for terrestrial
    bipeds like Homo, ISTM arboreal hominids like D.guggenmosi would have >> >> a much harder time living/migrating there.

    "is".
    Again, refer to microclimate of Levant 11ma - 5ma. Today's Dead Sea was once the vast brackish Lake Lisan that reached to Lebanon, a gallery forest may have reached from Anatolia to Egypt.
    The regions you describe above are part of the Mediterranean coastal
    mountains I mentioned previously.

    The Dead Sea is by no means a coastal mountain region. https://en.wikipedia.org/wiki/Judaean_Mountains

    These are part of a series of ranges all along the eastern
    Mediterranean coast.
    I agree a coastal Mediterranean
    forest is plausible.

    I'm referring to the tectonic rift valley between Zimbabwe/Zambia and Lebanon/Anatolia.
    ... which runs parallel to the Mediterranean coast.
    Of course, there were coastal forests as well, but they were affected by the MSC.

    However, my understanding is the evidence is
    insufficient to say if it would have been as extensive and continuous
    as you suggest during the time you suggest.

    Haven't got enough hard data yet.
    Cite the data you think is sufficient to answer this question.
    What is ISTM?


    It's shorthand acronym for "It Seems To Me"

    Ok, thanks.

    Danuvius, Rudapithecus, Graecopithecus, Oranopithecus each had a unique trait shared with hominins. I think of them as a superspecies with local variations.
    -
    If you place Danuvius half-way between fast brachiating bipedal long backed long achilles tendon hylobatids and bipedal Homo with long back and long achilles tendon, it fits perfectly.

    Wiki:
    Danuvius is thought to have had a broad chest. It is the first recorded Miocene great ape to have had the diaphragm located in the lower chest cavity, as in Homo, indicating an extended lower back and a greater number of functional lumbar
    vertebrae. This may have caused lordosis (the normal curvature of the human spine) and moved the center of mass over the hips and legs, which implies some habitual bipedal activity.

    The robust finger and hypertrophied wrist and elbow bones indicate a strong grip and load bearing adaptations for the arms. The legs also show adaptations for load-bearing, especially at the hypertrophied knee joint. There was likely limited
    ankle loading, and the ankle would have had a hinge-like function, being most stable if positioned perpendicularly to the leg as opposed to at an angle in apes. Danuvius was likely able to achieve a strong grip with its big toes, unlike modern African
    great apes, which would have allowed it to grasp onto thinner trees. The limb proportions are most similar to those of bonobos.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to daud.deden@gmail.com on Sat Nov 19 14:20:17 2022
    On Sat, 19 Nov 2022 06:06:22 -0800 (PST), Daud Deden
    <daud.deden@gmail.com> wrote:

    On Saturday, November 19, 2022 at 6:40:01 AM UTC-5, 69jp...@gmail.com wrote: >> On Fri, 18 Nov 2022 03:45:32 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, November 18, 2022 at 2:12:32 AM UTC-5, 69jp...@gmail.com wrote: >> >> On Thu, 17 Nov 2022 15:53:51 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 12:57:57 PM UTC-5, 69jp...@gmail.com wrote:
    On Wed, 16 Nov 2022 22:42:03 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 1:29:04 AM UTC-5, Daud Deden wrote:
    On Wednesday, November 16, 2022 at 11:08:11 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 04 Nov 2022 02:21:55 -0400, jillery <69jp...@gmail.com> >> >> >> >> > wrote:

    On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism. >> >> >> >> > >>> >> >>
    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a
    Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.


    My impression is there isn't enough evidence to show whether Pliocene
    African apes descended from Miocene European apes or Miocene African
    apes. Either way, there was enough time between the two eras to have
    evolved differences between either Miocene populations and Pliocene S.
    tchadensis.

    I have recently become aware of:

    <https://en.wikipedia.org/wiki/Danuvius_guggenmosi>

    which was a Miocene European ape that may have evolved arboreal >> >> >> >> > bipedalism similar to S.tchadensis.

    Depending on how widespread its range, and how successful its
    descendants, it's plausible they lived south of the Black Sea during
    the late Miocene.

    The question then becomes whether it's more likely these apes found
    their way into Africa to become the ancestors of Pliocene
    S.tchadensis, or whether S.tchadensis evolved from Miocene African
    apes.

    Unfortunately, the habitat of these apes made their fossil
    preservation extremely rare, and so the evidence to well support >> >> >> >> > either hypothesis is lacking.

    However, the question at least conditionally can be answered by >> >> >> >> > comparing the likelihood of a migratory pathway during that time,
    versus the likelihood of arboreal bipedalism evolving independently in
    two populations.

    There are a number of anatomic features associated with arboreal >> >> >> >> > bipedalism, some of which are necessary, ex. anterior foramen magnum,

    The foramen magnum is always situated relatively more anteriorly in immature than in mature apes.[ - and men. ]
    Not sure what you mean by "mature"; the individual or the species?

    Individually.
    My understanding is the relative position of foramen magnum doesn't
    change significantly during human development.

    Right. In chimps the muzzle gradually moves anteriorly relative to the foramen magnum, in Homo only the nose does.
    Sorry, I erred above, I'd meant "...than in mature apes." The "and men" was NOT meant, I thought I'd erased it! Oops.
    The positions of the muzzle and/or nose relative to the foramen magnum
    don't inform bipedalism.

    It does, in tail-less upright orthogonal striding terrestrial former/partial arboreal bipeds, it does not in hopping bipeds.
    Cf short-faced giant kangaroo (short tail, striding upright bipedal)


    The topic isn't general bipedalism, but hominoid bipedalism.
    Non-hominoid species don't inform this discussion.


    Either way, the important point is the position and angle of foramen >> >> >> magnum are diagnostic among all vertebrates for how they habitually >> >> >> hold their head, and so includes/excludes bipedalism among hominids. >> >> >
    Yes, but no. Great apes are bipedal except when (hurrying) on open ground they adopt quadrupedalism. Homo retains the primitive bipedal gait of hominoid ancestors, as do hylobatids.
    All Homo species are great apes by definition, including H.sapiens.

    Yes, I meant 'arboreal great apes'. Humans are terrestrial great apes, hylobatids are arboreal lesser apes.

    They do/did quadrupedalism only in exceptional cases.

    https://youtu.be/pCrH6BOwxe4 15mph qpal running as a patas monkey, not a chimp.
    Imagine how much faster that person would be if he ran normally, like
    this:

    <https://www.youtube.com/watch?v=k3PZgbQ8auE>
    How is that an exceptional case among hominins? Only Usain Bolt can outrun qpal chimp at top speed.


    Your cited video shows an exceptional case among humans, which have
    relatively short arms and long legs, anatomically maladapted for
    quadrupedal locomotion. Also, even though his head is in extreme
    elevation, he can barely see where he's going, as his foramen magnum
    is anatomically maladapted for quadrupedal motion. Silly Guinness
    records notwithstanding, any human moving quadrupedally from a
    predator would soon become predator poop.


    and some of which are incidental, ex. molar patterns. Descendant >> >> >> >> > populations are more likely to share these features than are
    independent populations. This suggests to me that a sufficiently >> >> >> >> > robust fossil record could answer this question with some degree of
    certainty.

    Alternately, my understanding is southern Europe and central Africa
    are ecological opposites, in the sense that when one is hot and dry
    the other is temperate and wet.
    Central Africa is and was hot,
    ... and wet aka tropical,

    The adoption of qpal knucklewalking by African apes indicates that their ancient habitat went through a dry phase (rainforest became patchy) forcing a terrestrial dog-like gait.
    Perhaps. My understanding is bipedal arboreal apes continued to walk
    bipedally on the ground, while non-bipedal arboreal apes also adopted
    quadrupedal habits on the ground.

    Bipedal walking is primitive in arboreal hominoids, quadrupedal walking is derived. I don't know of any 'non-bipedal arboreal apes', only monkeys.
    That's not my understanding. My understanding is chimpanzees,
    gorillas, and orangutans are non-bipedal arboreal apes, meaning when
    they are in the trees, they do not walk upright.

    Their body orientation on and under branches is primarily upright, not pronograde with all limbs in compression aka quadrupedal. The modern AMHs orthogonal posture is derived, not the same as primitive upright bipedal arboreal hominoids.


    You continue to use above a non-standard meaning of bipedalism.
    Hanging from branches using combinations of limbs isn't bipedalism any
    more than is climbing up coconut palms.


    As were most
    arboreal apes prior to Australopithecines.
    just right for the evolution of small bipedal arboreal apes.

    The fact that there are no small bipedal arboreal apes in Africa indicates that there was some climate shifting.
    Again perhaps. It also suggests small bipedal arboreal apes were
    outcompeted.

    They were, by monkeys which were more ground adapted, able to swiftly run between forest stands during a drier climate phase.

    the southern Black Sea is between temperate and tropical.
    Correct. Southern Europe and the Black Sea are at the same latitudes. >> >> >> This suggests they would tend to have the same climate. However, the >> >> >> Black Sea is farther inland, and so suffers more continental extremes.
    So any climate changes will appear first around the Black Sea and
    become more extreme compared to southern Europe.

    I'm talking about from 11ma through the MSC to 5ma. The Medit. & Red Seas dried out, the Black Sea didn't.
    The relative position of the Black Sea didn't change from then to now. >> >> The important point is its position is deep in Eurasia, where
    continental climates rule.

    It lies between the Atlantic-Mediterranean and the Caspian Sea, in the Peri-Tethyan basin, protected by the high Iranian plateau to the south. Not a typical continental climate.
    <https://www.britannica.com/place/Black-Sea/Climate>
    **********************************
    The climate of the landlocked Black Sea can be characterized generally
    as continental (i.e., subject to pronounced seasonal temperature
    variations), although climatic conditions in some parts of the basin
    are controlled to a great extent by the shoreline relief. A steppe
    climate, with cold winters and hot, dry summers, is found in the
    northwestern part of the basin exposed to the influence of air masses
    from the north.
    ************************************

    Summer in north including Bavaria via Danube valley, winter in south including visits further southwardly.


    I suppose Miocene apes collected frequent-flier miles.


    My understanding is the Mediterranean dried out only about 6mya, long
    after European, and presumably Black Sea, arboreal apes went extinct.

    No, Danuvius and later Miocene apes there were of one lineage IMO, that may have lived there until 5ma, with successive expansional waves emigrating outwardly including towards Africa.

    The Red Sea is too far south to affect migration from Europe to Africa >> >> regardless of climate patterns.

    It is part of the African-Anatolian rift.
    I acknowledge that rift was one plausible pathway from Europe to
    Africa. The Red Sea was not, nor did it block such a pathway.

    I include it provisionally, more data needed.


    Sounds like a segue for aquatic ape hypothesis.


    Moving toward 30 degrees latitude, rainfall becomes seasonally dry, >> >> >> and then almost continuously dry. My understanding is, the only
    native forests south of the Caspian are in the mountains, and adjacent
    to the Mediterranean coasts. Arboreal apes of any kind would find
    these deserts impassible.

    You are speaking of recent climate. There are no arboreal apes there now.
    No, I am speaking of climate then *and* now. Regions around 30
    degrees latitude tend to be drier than those around the equator, with
    exceptions due to terrain and ocean currents.

    Stop temporarily.


    Unclear. Do you mean stop migration temporarily? If so, keep in mind
    that the same climate changes which would create arid conditions
    around 30 degrees latitude would also shrink forests further north and
    south.


    You appear to be claiming that the European Miocene apes could never have been linked to African and Asian apes. Yet they certainly were, else they wouldn't have existed at all.
    Such an "appearance" is incorrect. In certain cases, regions around
    30 degrees latitude have/had enough rainfall to support forests. The
    relevant point here is, global climate since the Miocene has gotten
    colder and drier, especially around 30 degrees latitude, which has led
    to the creation of large areas of treeless savannah and desert. I
    don't know when European and African forests separated. Do you?

    Also, the question isn't about the origin of apes generally. It's
    about the origin of arboreal bipedal apes. We know they existed in
    Pliocene Africa. They *may* have existed in Miocene Europe. Even if
    they did, the two populations may still have evolved independently.
    To a first approximation, average rainfall and temperature are
    functions of latitude. However, while temperature is a function of
    the sine of latitude, rainfall is more complex. It tends to be
    continuously heavy near the equator, continuously dry near 30 degrees,
    and seasonally variable between 30 and 60 degrees. This general
    pattern is modified, sometimes dramatically, by terrain, ocean
    currents, seasons, and Milankovitch cycles.

    The most significant variable is Africa's northward tectonic
    migration, about a centimeter a year since before the Miocene. So,
    while central Africa has moved from south to north of the equator with
    little effect, north Africa has approached and then went north of 30 >> >> >> degrees, making it over time ever drier, amplifying other climate
    trends, making once wooded areas into vast savannah and desert.

    Yes.

    Also, Africa's tectonic slide north almost certainly pinched closed >> >> >> the Gilbraltar Sttraits, which caused the Mediterranean to dry up at >> >> >> least once, and likely several times as sea levels rose and fell. The >> >> >> resulting hot salt basin would also have been impassible for arboreal >> >> >> apes.
    This is as true now as it was in the
    Miocene. This suggests to me there could not have been an unbroken
    forested path for arboreal apes to migrate between Europe/Near East
    and Central Africa.
    I would not claim nor disclaim that. The Levant is near the midpoint, extends the African Rift valley to Anatolia, is a major avian migration route between Africa and Eurasia, has fossil/artifacts of Homo erectus, neanderthal & sapiens oldest
    known cooking (fish .78ma) and earliest waternut gathering and bread making. The region is amenable to hominins & Homo.
    I acknowledge the facts you describe above. However, the Levant is
    savannah and desert except for a narrow strip along the Mediterranean >> >> >> and up in the mountains. While this is no problem for terrestrial
    bipeds like Homo, ISTM arboreal hominids like D.guggenmosi would have >> >> >> a much harder time living/migrating there.

    "is".
    Again, refer to microclimate of Levant 11ma - 5ma. Today's Dead Sea was once the vast brackish Lake Lisan that reached to Lebanon, a gallery forest may have reached from Anatolia to Egypt.
    The regions you describe above are part of the Mediterranean coastal
    mountains I mentioned previously.

    The Dead Sea is by no means a coastal mountain region.
    https://en.wikipedia.org/wiki/Judaean_Mountains

    These are part of a series of ranges all along the eastern
    Mediterranean coast.
    I agree a coastal Mediterranean
    forest is plausible.

    I'm referring to the tectonic rift valley between Zimbabwe/Zambia and Lebanon/Anatolia.
    ... which runs parallel to the Mediterranean coast.
    Of course, there were coastal forests as well, but they were affected by the MSC.

    However, my understanding is the evidence is
    insufficient to say if it would have been as extensive and continuous
    as you suggest during the time you suggest.

    Haven't got enough hard data yet.
    Cite the data you think is sufficient to answer this question.
    What is ISTM?


    It's shorthand acronym for "It Seems To Me"

    Ok, thanks.

    Danuvius, Rudapithecus, Graecopithecus, Oranopithecus each had a unique trait shared with hominins. I think of them as a superspecies with local variations.
    -
    If you place Danuvius half-way between fast brachiating bipedal long backed long achilles tendon hylobatids and bipedal Homo with long back and long achilles tendon, it fits perfectly.

    Wiki:
    Danuvius is thought to have had a broad chest. It is the first recorded Miocene great ape to have had the diaphragm located in the lower chest cavity, as in Homo, indicating an extended lower back and a greater number of functional lumbar
    vertebrae. This may have caused lordosis (the normal curvature of the human spine) and moved the center of mass over the hips and legs, which implies some habitual bipedal activity.

    The robust finger and hypertrophied wrist and elbow bones indicate a strong grip and load bearing adaptations for the arms. The legs also show adaptations for load-bearing, especially at the hypertrophied knee joint. There was likely limited
    ankle loading, and the ankle would have had a hinge-like function, being most stable if positioned perpendicularly to the leg as opposed to at an angle in apes. Danuvius was likely able to achieve a strong grip with its big toes, unlike modern African
    great apes, which would have allowed it to grasp onto thinner trees. The limb proportions are most similar to those of bonobos.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Sat Nov 19 12:48:18 2022
    On Saturday, November 19, 2022 at 2:20:20 PM UTC-5, 69jp...@gmail.com wrote:
    On Sat, 19 Nov 2022 06:06:22 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Saturday, November 19, 2022 at 6:40:01 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 18 Nov 2022 03:45:32 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, November 18, 2022 at 2:12:32 AM UTC-5, 69jp...@gmail.com wrote:
    On Thu, 17 Nov 2022 15:53:51 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 12:57:57 PM UTC-5, 69jp...@gmail.com wrote:
    On Wed, 16 Nov 2022 22:42:03 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 1:29:04 AM UTC-5, Daud Deden wrote:
    On Wednesday, November 16, 2022 at 11:08:11 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 04 Nov 2022 02:21:55 -0400, jillery <69jp...@gmail.com>
    wrote:

    On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a
    Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.


    My impression is there isn't enough evidence to show whether Pliocene
    African apes descended from Miocene European apes or Miocene African
    apes. Either way, there was enough time between the two eras to have
    evolved differences between either Miocene populations and Pliocene S.
    tchadensis.

    I have recently become aware of:

    <https://en.wikipedia.org/wiki/Danuvius_guggenmosi>

    which was a Miocene European ape that may have evolved arboreal
    bipedalism similar to S.tchadensis.

    Depending on how widespread its range, and how successful its >> >> >> >> > descendants, it's plausible they lived south of the Black Sea during
    the late Miocene.

    The question then becomes whether it's more likely these apes found
    their way into Africa to become the ancestors of Pliocene
    S.tchadensis, or whether S.tchadensis evolved from Miocene African
    apes.

    Unfortunately, the habitat of these apes made their fossil
    preservation extremely rare, and so the evidence to well support
    either hypothesis is lacking.

    However, the question at least conditionally can be answered by
    comparing the likelihood of a migratory pathway during that time,
    versus the likelihood of arboreal bipedalism evolving independently in
    two populations.

    There are a number of anatomic features associated with arboreal
    bipedalism, some of which are necessary, ex. anterior foramen magnum,

    The foramen magnum is always situated relatively more anteriorly in immature than in mature apes.[ - and men. ]
    Not sure what you mean by "mature"; the individual or the species? >> >> >
    Individually.
    My understanding is the relative position of foramen magnum doesn't
    change significantly during human development.

    Right. In chimps the muzzle gradually moves anteriorly relative to the foramen magnum, in Homo only the nose does.
    Sorry, I erred above, I'd meant "...than in mature apes." The "and men" was NOT meant, I thought I'd erased it! Oops.
    The positions of the muzzle and/or nose relative to the foramen magnum
    don't inform bipedalism.

    It does, in tail-less upright orthogonal striding terrestrial former/partial arboreal bipeds, it does not in hopping bipeds.
    Cf short-faced giant kangaroo (short tail, striding upright bipedal)
    The topic isn't general bipedalism, but hominoid bipedalism.
    Non-hominoid species don't inform this discussion.
    Either way, the important point is the position and angle of foramen
    magnum are diagnostic among all vertebrates for how they habitually >> >> >> hold their head, and so includes/excludes bipedalism among hominids.

    Yes, but no. Great apes are bipedal except when (hurrying) on open ground they adopt quadrupedalism. Homo retains the primitive bipedal gait of hominoid ancestors, as do hylobatids.
    All Homo species are great apes by definition, including H.sapiens.

    Yes, I meant 'arboreal great apes'. Humans are terrestrial great apes, hylobatids are arboreal lesser apes.

    They do/did quadrupedalism only in exceptional cases.

    https://youtu.be/pCrH6BOwxe4 15mph qpal running as a patas monkey, not a chimp.
    Imagine how much faster that person would be if he ran normally, like
    this:

    <https://www.youtube.com/watch?v=k3PZgbQ8auE>
    How is that an exceptional case among hominins? Only Usain Bolt can outrun qpal chimp at top speed.
    Your cited video shows an exceptional case among humans, which have relatively short arms and long legs, anatomically maladapted for
    quadrupedal locomotion. Also, even though his head is in extreme
    elevation, he can barely see where he's going, as his foramen magnum
    is anatomically maladapted for quadrupedal motion. Silly Guinness
    records notwithstanding, any human moving quadrupedally from a
    predator would soon become predator poop.
    and some of which are incidental, ex. molar patterns. Descendant
    populations are more likely to share these features than are >> >> >> >> > independent populations. This suggests to me that a sufficiently
    robust fossil record could answer this question with some degree of
    certainty.

    Alternately, my understanding is southern Europe and central Africa
    are ecological opposites, in the sense that when one is hot and dry
    the other is temperate and wet.
    Central Africa is and was hot,
    ... and wet aka tropical,

    The adoption of qpal knucklewalking by African apes indicates that their ancient habitat went through a dry phase (rainforest became patchy) forcing a terrestrial dog-like gait.
    Perhaps. My understanding is bipedal arboreal apes continued to walk >> >> bipedally on the ground, while non-bipedal arboreal apes also adopted >> >> quadrupedal habits on the ground.

    Bipedal walking is primitive in arboreal hominoids, quadrupedal walking is derived. I don't know of any 'non-bipedal arboreal apes', only monkeys.
    That's not my understanding. My understanding is chimpanzees,
    gorillas, and orangutans are non-bipedal arboreal apes, meaning when
    they are in the trees, they do not walk upright.

    Their body orientation on and under branches is primarily upright, not pronograde with all limbs in compression aka quadrupedal. The modern AMHs orthogonal posture is derived, not the same as primitive upright bipedal arboreal hominoids.
    You continue to use above a non-standard meaning of bipedalism.
    Hanging from branches using combinations of limbs isn't bipedalism any
    more than is climbing up coconut palms.
    As were most
    arboreal apes prior to Australopithecines.
    just right for the evolution of small bipedal arboreal apes.

    The fact that there are no small bipedal arboreal apes in Africa indicates that there was some climate shifting.
    Again perhaps. It also suggests small bipedal arboreal apes were
    outcompeted.

    They were, by monkeys which were more ground adapted, able to swiftly run between forest stands during a drier climate phase.

    the southern Black Sea is between temperate and tropical.
    Correct. Southern Europe and the Black Sea are at the same latitudes.
    This suggests they would tend to have the same climate. However, the
    Black Sea is farther inland, and so suffers more continental extremes.
    So any climate changes will appear first around the Black Sea and >> >> >> become more extreme compared to southern Europe.

    I'm talking about from 11ma through the MSC to 5ma. The Medit. & Red Seas dried out, the Black Sea didn't.
    The relative position of the Black Sea didn't change from then to now. >> >> The important point is its position is deep in Eurasia, where
    continental climates rule.

    It lies between the Atlantic-Mediterranean and the Caspian Sea, in the Peri-Tethyan basin, protected by the high Iranian plateau to the south. Not a typical continental climate.
    <https://www.britannica.com/place/Black-Sea/Climate>
    **********************************
    The climate of the landlocked Black Sea can be characterized generally
    as continental (i.e., subject to pronounced seasonal temperature
    variations), although climatic conditions in some parts of the basin
    are controlled to a great extent by the shoreline relief. A steppe
    climate, with cold winters and hot, dry summers, is found in the
    northwestern part of the basin exposed to the influence of air masses
    from the north.
    ************************************

    Summer in north including Bavaria via Danube valley, winter in south including visits further southwardly.
    I suppose Miocene apes collected frequent-flier miles.
    My understanding is the Mediterranean dried out only about 6mya, long >> >> after European, and presumably Black Sea, arboreal apes went extinct. >> >
    No, Danuvius and later Miocene apes there were of one lineage IMO, that may have lived there until 5ma, with successive expansional waves emigrating outwardly including towards Africa.

    The Red Sea is too far south to affect migration from Europe to Africa >> >> regardless of climate patterns.

    It is part of the African-Anatolian rift.
    I acknowledge that rift was one plausible pathway from Europe to
    Africa. The Red Sea was not, nor did it block such a pathway.

    I include it provisionally, more data needed.
    Sounds like a segue for aquatic ape hypothesis.
    Moving toward 30 degrees latitude, rainfall becomes seasonally dry, >> >> >> and then almost continuously dry. My understanding is, the only
    native forests south of the Caspian are in the mountains, and adjacent
    to the Mediterranean coasts. Arboreal apes of any kind would find >> >> >> these deserts impassible.

    You are speaking of recent climate. There are no arboreal apes there now.
    No, I am speaking of climate then *and* now. Regions around 30
    degrees latitude tend to be drier than those around the equator, with >> >> exceptions due to terrain and ocean currents.

    Stop temporarily.

    Sorry, I'm on buses today around town, some w wifi, others not. I meant BRB be right back.

    Unclear. Do you mean stop migration temporarily? If so, keep in mind
    that the same climate changes which would create arid conditions
    around 30 degrees latitude would also shrink forests further north and south.
    You appear to be claiming that the European Miocene apes could never have been linked to African and Asian apes. Yet they certainly were, else they wouldn't have existed at all.
    Such an "appearance" is incorrect. In certain cases, regions around
    30 degrees latitude have/had enough rainfall to support forests. The
    relevant point here is, global climate since the Miocene has gotten
    colder and drier, especially around 30 degrees latitude, which has led
    to the creation of large areas of treeless savannah and desert. I
    don't know when European and African forests separated. Do you?

    Also, the question isn't about the origin of apes generally. It's
    about the origin of arboreal bipedal apes. We know they existed in
    Pliocene Africa. They *may* have existed in Miocene Europe. Even if
    they did, the two populations may still have evolved independently.
    To a first approximation, average rainfall and temperature are
    functions of latitude. However, while temperature is a function of >> >> >> the sine of latitude, rainfall is more complex. It tends to be
    continuously heavy near the equator, continuously dry near 30 degrees,
    and seasonally variable between 30 and 60 degrees. This general
    pattern is modified, sometimes dramatically, by terrain, ocean
    currents, seasons, and Milankovitch cycles.

    The most significant variable is Africa's northward tectonic
    migration, about a centimeter a year since before the Miocene. So, >> >> >> while central Africa has moved from south to north of the equator with
    little effect, north Africa has approached and then went north of 30
    degrees, making it over time ever drier, amplifying other climate >> >> >> trends, making once wooded areas into vast savannah and desert.

    Yes.

    Also, Africa's tectonic slide north almost certainly pinched closed >> >> >> the Gilbraltar Sttraits, which caused the Mediterranean to dry up at
    least once, and likely several times as sea levels rose and fell. The
    resulting hot salt basin would also have been impassible for arboreal
    apes.
    This is as true now as it was in the
    Miocene. This suggests to me there could not have been an unbroken
    forested path for arboreal apes to migrate between Europe/Near East
    and Central Africa.
    I would not claim nor disclaim that. The Levant is near the midpoint, extends the African Rift valley to Anatolia, is a major avian migration route between Africa and Eurasia, has fossil/artifacts of Homo erectus, neanderthal & sapiens
    oldest known cooking (fish .78ma) and earliest waternut gathering and bread making. The region is amenable to hominins & Homo.
    I acknowledge the facts you describe above. However, the Levant is >> >> >> savannah and desert except for a narrow strip along the Mediterranean
    and up in the mountains. While this is no problem for terrestrial >> >> >> bipeds like Homo, ISTM arboreal hominids like D.guggenmosi would have
    a much harder time living/migrating there.

    "is".
    Again, refer to microclimate of Levant 11ma - 5ma. Today's Dead Sea was once the vast brackish Lake Lisan that reached to Lebanon, a gallery forest may have reached from Anatolia to Egypt.
    The regions you describe above are part of the Mediterranean coastal >> >> mountains I mentioned previously.

    The Dead Sea is by no means a coastal mountain region.
    https://en.wikipedia.org/wiki/Judaean_Mountains

    These are part of a series of ranges all along the eastern
    Mediterranean coast.
    I agree a coastal Mediterranean
    forest is plausible.

    I'm referring to the tectonic rift valley between Zimbabwe/Zambia and Lebanon/Anatolia.
    ... which runs parallel to the Mediterranean coast.
    Of course, there were coastal forests as well, but they were affected by the MSC.

    However, my understanding is the evidence is
    insufficient to say if it would have been as extensive and continuous >> >> as you suggest during the time you suggest.

    Haven't got enough hard data yet.
    Cite the data you think is sufficient to answer this question.
    What is ISTM?


    It's shorthand acronym for "It Seems To Me"

    Ok, thanks.

    Danuvius, Rudapithecus, Graecopithecus, Oranopithecus each had a unique trait shared with hominins. I think of them as a superspecies with local variations.
    -
    If you place Danuvius half-way between fast brachiating bipedal long backed long achilles tendon hylobatids and bipedal Homo with long back and long achilles tendon, it fits perfectly.

    Wiki:
    Danuvius is thought to have had a broad chest. It is the first recorded Miocene great ape to have had the diaphragm located in the lower chest cavity, as in Homo, indicating an extended lower back and a greater number of functional lumbar
    vertebrae. This may have caused lordosis (the normal curvature of the human spine) and moved the center of mass over the hips and legs, which implies some habitual bipedal activity.

    The robust finger and hypertrophied wrist and elbow bones indicate a strong grip and load bearing adaptations for the arms. The legs also show adaptations for load-bearing, especially at the hypertrophied knee joint. There was likely limited
    ankle loading, and the ankle would have had a hinge-like function, being most stable if positioned perpendicularly to the leg as opposed to at an angle in apes. Danuvius was likely able to achieve a strong grip with its big toes, unlike modern African
    great apes, which would have allowed it to grasp onto thinner trees. The limb proportions are most similar to those of bonobos.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Sat Nov 19 12:43:27 2022
    On Saturday, November 19, 2022 at 2:20:20 PM UTC-5, 69jp...@gmail.com wrote:
    On Sat, 19 Nov 2022 06:06:22 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Saturday, November 19, 2022 at 6:40:01 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 18 Nov 2022 03:45:32 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, November 18, 2022 at 2:12:32 AM UTC-5, 69jp...@gmail.com wrote:
    On Thu, 17 Nov 2022 15:53:51 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 12:57:57 PM UTC-5, 69jp...@gmail.com wrote:
    On Wed, 16 Nov 2022 22:42:03 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 1:29:04 AM UTC-5, Daud Deden wrote:
    On Wednesday, November 16, 2022 at 11:08:11 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 04 Nov 2022 02:21:55 -0400, jillery <69jp...@gmail.com>
    wrote:

    On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a
    Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.


    My impression is there isn't enough evidence to show whether Pliocene
    African apes descended from Miocene European apes or Miocene African
    apes. Either way, there was enough time between the two eras to have
    evolved differences between either Miocene populations and Pliocene S.
    tchadensis.

    I have recently become aware of:

    <https://en.wikipedia.org/wiki/Danuvius_guggenmosi>

    which was a Miocene European ape that may have evolved arboreal
    bipedalism similar to S.tchadensis.

    Depending on how widespread its range, and how successful its >> >> >> >> > descendants, it's plausible they lived south of the Black Sea during
    the late Miocene.

    The question then becomes whether it's more likely these apes found
    their way into Africa to become the ancestors of Pliocene
    S.tchadensis, or whether S.tchadensis evolved from Miocene African
    apes.

    Unfortunately, the habitat of these apes made their fossil
    preservation extremely rare, and so the evidence to well support
    either hypothesis is lacking.

    However, the question at least conditionally can be answered by
    comparing the likelihood of a migratory pathway during that time,
    versus the likelihood of arboreal bipedalism evolving independently in
    two populations.

    There are a number of anatomic features associated with arboreal
    bipedalism, some of which are necessary, ex. anterior foramen magnum,

    The foramen magnum is always situated relatively more anteriorly in immature than in mature apes.[ - and men. ]
    Not sure what you mean by "mature"; the individual or the species? >> >> >
    Individually.
    My understanding is the relative position of foramen magnum doesn't
    change significantly during human development.

    Right. In chimps the muzzle gradually moves anteriorly relative to the foramen magnum, in Homo only the nose does.
    Sorry, I erred above, I'd meant "...than in mature apes." The "and men" was NOT meant, I thought I'd erased it! Oops.
    The positions of the muzzle and/or nose relative to the foramen magnum
    don't inform bipedalism.

    It does, in tail-less upright orthogonal striding terrestrial former/partial arboreal bipeds, it does not in hopping bipeds.
    Cf short-faced giant kangaroo (short tail, striding upright bipedal)
    The topic isn't general bipedalism, but hominoid bipedalism.
    Non-hominoid species don't inform this discussion.
    Either way, the important point is the position and angle of foramen
    magnum are diagnostic among all vertebrates for how they habitually >> >> >> hold their head, and so includes/excludes bipedalism among hominids.

    Yes, but no. Great apes are bipedal except when (hurrying) on open ground they adopt quadrupedalism. Homo retains the primitive bipedal gait of hominoid ancestors, as do hylobatids.
    All Homo species are great apes by definition, including H.sapiens.

    Yes, I meant 'arboreal great apes'. Humans are terrestrial great apes, hylobatids are arboreal lesser apes.

    They do/did quadrupedalism only in exceptional cases.

    https://youtu.be/pCrH6BOwxe4 15mph qpal running as a patas monkey, not a chimp.
    Imagine how much faster that person would be if he ran normally, like
    this:

    <https://www.youtube.com/watch?v=k3PZgbQ8auE>
    How is that an exceptional case among hominins? Only Usain Bolt can outrun qpal chimp at top speed.
    Your cited video shows an exceptional case among humans, which have relatively short arms and long legs, anatomically maladapted for
    quadrupedal locomotion.

    Humans are faster qpal palm-down sprinter and qpal endurance runner than any other hominoid.
    Patas monkey's arms are shorter than their legs: https://www.britannica.com/animal/patas-monkey

    Locomotor Anatomy and Behavior of Patas Monkeys (Erythrocebus patas) with Comparison to Vervet Monkeys (Cercopithecus aethiops)
    Adrienne L. Zihlman and Carol E. Underwood

    Additional article information

    Abstract
    Patas monkeys (Erythrocebus patas) living in African savanna woodlands and grassland habitats have a locomotor system that allows them to run fast, presumably to avoid predators. Long fore- and hindlimbs, long foot bones, short toes, and a digitigrade
    foot posture were proposed as anatomical correlates with speed. In addition to skeletal proportions, soft tissue and whole body proportions are important components of the locomotor system. To further distinguish patas anatomy from other Old World
    monkeys, a comparative study based on dissection of skin, muscle, and bone from complete individuals of patas and vervet monkeys (Cercopithecus aethiops) was undertaken. Analysis reveals that small adjustments in patas skeletal proportions, relative mass
    of limbs and tail, and specific muscle groups promote efficient sagittal limb motion. The ability to run fast is based on a locomotor system adapted for long distance walking. The patas' larger home range and longer daily range than those of vervets give
    them access to highly dispersed, nutritious foods, water, and sleeping trees. Furthermore, patas monkeys have physiological adaptations that enable them to tolerate and dissipate heat. These features all contribute to the distinct adaptation that is the
    patas monkeys' basis for survival in grassland and savanna woodland areas.

    Also, even though his head is in extreme
    elevation, he can barely see where he's going, as his foramen magnum
    is anatomically maladapted for quadrupedal motion. Silly Guinness
    records notwithstanding, any human moving quadrupedally from a
    predator would soon become predator poop.

    Why? Carrying a blade pirate-style teeth-clenched, with a few pards similarly equipped, would present predators with a serious challenge. Bipedally, better weapons could be carried, of course, but running itself isn't enough. Patas, verbet & baboons
    climb trees, qpal running is just the short sprint to flight.

    and some of which are incidental, ex. molar patterns. Descendant
    populations are more likely to share these features than are >> >> >> >> > independent populations. This suggests to me that a sufficiently
    robust fossil record could answer this question with some degree of
    certainty.

    Alternately, my understanding is southern Europe and central Africa
    are ecological opposites, in the sense that when one is hot and dry
    the other is temperate and wet.
    Central Africa is and was hot,
    ... and wet aka tropical,

    The adoption of qpal knucklewalking by African apes indicates that their ancient habitat went through a dry phase (rainforest became patchy) forcing a terrestrial dog-like gait.
    Perhaps. My understanding is bipedal arboreal apes continued to walk >> >> bipedally on the ground, while non-bipedal arboreal apes also adopted >> >> quadrupedal habits on the ground.

    Bipedal walking is primitive in arboreal hominoids, quadrupedal walking is derived. I don't know of any 'non-bipedal arboreal apes', only monkeys.
    That's not my understanding. My understanding is chimpanzees,
    gorillas, and orangutans are non-bipedal arboreal apes, meaning when
    they are in the trees, they do not walk upright.

    Their body orientation on and under branches is primarily upright, not pronograde with all limbs in compression aka quadrupedal. The modern AMHs orthogonal posture is derived, not the same as primitive upright bipedal arboreal hominoids.
    You continue to use above a non-standard meaning of bipedalism.

    Please direct me to "a standard meaning of bipedalism". Afaik, bipedalism is a trait of locomoting on 2 legs in compression, whether the hands are swinging, carrying or plucking.
    Sloths are quadrumanual, orangs are also called that when hanging tensionally from four limbs, but bipedal when walking on thick branches.

    Hanging from branches using combinations of limbs isn't bipedalism any
    more than is climbing up coconut palms.

    Suspension itself is not bipedalism.

    As were most
    arboreal apes prior to Australopithecines.
    just right for the evolution of small bipedal arboreal apes.

    The fact that there are no small bipedal arboreal apes in Africa indicates that there was some climate shifting.
    Again perhaps. It also suggests small bipedal arboreal apes were
    outcompeted.

    They were, by monkeys which were more ground adapted, able to swiftly run between forest stands during a drier climate phase.

    the southern Black Sea is between temperate and tropical.
    Correct. Southern Europe and the Black Sea are at the same latitudes.
    This suggests they would tend to have the same climate. However, the
    Black Sea is farther inland, and so suffers more continental extremes.
    So any climate changes will appear first around the Black Sea and >> >> >> become more extreme compared to southern Europe.

    I'm talking about from 11ma through the MSC to 5ma. The Medit. & Red Seas dried out, the Black Sea didn't.
    The relative position of the Black Sea didn't change from then to now. >> >> The important point is its position is deep in Eurasia, where
    continental climates rule.

    It lies between the Atlantic-Mediterranean and the Caspian Sea, in the Peri-Tethyan basin, protected by the high Iranian plateau to the south. Not a typical continental climate.
    <https://www.britannica.com/place/Black-Sea/Climate>
    **********************************
    The climate of the landlocked Black Sea can be characterized generally
    as continental (i.e., subject to pronounced seasonal temperature
    variations), although climatic conditions in some parts of the basin
    are controlled to a great extent by the shoreline relief. A steppe
    climate, with cold winters and hot, dry summers, is found in the
    northwestern part of the basin exposed to the influence of air masses
    from the north.
    ************************************

    Summer in north including Bavaria via Danube valley, winter in south including visits further southwardly.
    I suppose Miocene apes collected frequent-flier miles.
    They weren't sessile, but very mobile.

    My understanding is the Mediterranean dried out only about 6mya, long >> >> after European, and presumably Black Sea, arboreal apes went extinct. >> >
    No, Danuvius and later Miocene apes there were of one lineage IMO, that may have lived there until 5ma, with successive expansional waves emigrating outwardly including towards Africa.

    The Red Sea is too far south to affect migration from Europe to Africa >> >> regardless of climate patterns.

    It is part of the African-Anatolian rift.
    I acknowledge that rift was one plausible pathway from Europe to
    Africa. The Red Sea was not, nor did it block such a pathway.

    I include it provisionally, more data needed.
    Sounds like a segue for aquatic ape hypothesis.

    Most proponents of that hypothesis tend to refuse to acknowledge that all extant (and by extension, archaic) Homo sleep well sheltered (dry, warm, shielded) from the elements (or try to be). Thus it is unrealistic imo.
    Of course, I refer to the surrounding region, which today is hyper-arid


    Moving toward 30 degrees latitude, rainfall becomes seasonally dry, >> >> >> and then almost continuously dry. My understanding is, the only
    native forests south of the Caspian are in the mountains, and adjacent
    to the Mediterranean coasts. Arboreal apes of any kind would find >> >> >> these deserts impassible.

    You are speaking of recent climate. There are no arboreal apes there now.
    No, I am speaking of climate then *and* now. Regions around 30
    degrees latitude tend to be drier than those around the equator, with >> >> exceptions due to terrain and ocean currents.
    Another stop.
    Stop temporarily.
    Unclear. Do you mean stop migration temporarily? If so, keep in mind
    that the same climate changes which would create arid conditions
    around 30 degrees latitude would also shrink forests further north and south.
    You appear to be claiming that the European Miocene apes could never have been linked to African and Asian apes. Yet they certainly were, else they wouldn't have existed at all.
    Such an "appearance" is incorrect. In certain cases, regions around
    30 degrees latitude have/had enough rainfall to support forests. The
    relevant point here is, global climate since the Miocene has gotten
    colder and drier, especially around 30 degrees latitude, which has led
    to the creation of large areas of treeless savannah and desert. I
    don't know when European and African forests separated. Do you?

    Also, the question isn't about the origin of apes generally. It's
    about the origin of arboreal bipedal apes. We know they existed in
    Pliocene Africa. They *may* have existed in Miocene Europe. Even if
    they did, the two populations may still have evolved independently.
    To a first approximation, average rainfall and temperature are
    functions of latitude. However, while temperature is a function of >> >> >> the sine of latitude, rainfall is more complex. It tends to be
    continuously heavy near the equator, continuously dry near 30 degrees,
    and seasonally variable between 30 and 60 degrees. This general
    pattern is modified, sometimes dramatically, by terrain, ocean
    currents, seasons, and Milankovitch cycles.

    The most significant variable is Africa's northward tectonic
    migration, about a centimeter a year since before the Miocene. So, >> >> >> while central Africa has moved from south to north of the equator with
    little effect, north Africa has approached and then went north of 30
    degrees, making it over time ever drier, amplifying other climate >> >> >> trends, making once wooded areas into vast savannah and desert.

    Yes.

    Also, Africa's tectonic slide north almost certainly pinched closed >> >> >> the Gilbraltar Sttraits, which caused the Mediterranean to dry up at
    least once, and likely several times as sea levels rose and fell. The
    resulting hot salt basin would also have been impassible for arboreal
    apes.
    This is as true now as it was in the
    Miocene. This suggests to me there could not have been an unbroken
    forested path for arboreal apes to migrate between Europe/Near East
    and Central Africa.
    I would not claim nor disclaim that. The Levant is near the midpoint, extends the African Rift valley to Anatolia, is a major avian migration route between Africa and Eurasia, has fossil/artifacts of Homo erectus, neanderthal & sapiens
    oldest known cooking (fish .78ma) and earliest waternut gathering and bread making. The region is amenable to hominins & Homo.
    I acknowledge the facts you describe above. However, the Levant is >> >> >> savannah and desert except for a narrow strip along the Mediterranean
    and up in the mountains. While this is no problem for terrestrial >> >> >> bipeds like Homo, ISTM arboreal hominids like D.guggenmosi would have
    a much harder time living/migrating there.

    "is".
    Again, refer to microclimate of Levant 11ma - 5ma. Today's Dead Sea was once the vast brackish Lake Lisan that reached to Lebanon, a gallery forest may have reached from Anatolia to Egypt.
    The regions you describe above are part of the Mediterranean coastal >> >> mountains I mentioned previously.

    The Dead Sea is by no means a coastal mountain region.
    https://en.wikipedia.org/wiki/Judaean_Mountains

    These are part of a series of ranges all along the eastern
    Mediterranean coast.
    I agree a coastal Mediterranean
    forest is plausible.

    I'm referring to the tectonic rift valley between Zimbabwe/Zambia and Lebanon/Anatolia.
    ... which runs parallel to the Mediterranean coast.
    Of course, there were coastal forests as well, but they were affected by the MSC.

    However, my understanding is the evidence is
    insufficient to say if it would have been as extensive and continuous >> >> as you suggest during the time you suggest.

    Haven't got enough hard data yet.
    Cite the data you think is sufficient to answer this question.
    What is ISTM?


    It's shorthand acronym for "It Seems To Me"

    Ok, thanks.

    Danuvius, Rudapithecus, Graecopithecus, Oranopithecus each had a unique trait shared with hominins. I think of them as a superspecies with local variations.
    -
    If you place Danuvius half-way between fast brachiating bipedal long backed long achilles tendon hylobatids and bipedal Homo with long back and long achilles tendon, it fits perfectly.

    Wiki:
    Danuvius is thought to have had a broad chest. It is the first recorded Miocene great ape to have had the diaphragm located in the lower chest cavity, as in Homo, indicating an extended lower back and a greater number of functional lumbar
    vertebrae. This may have caused lordosis (the normal curvature of the human spine) and moved the center of mass over the hips and legs, which implies some habitual bipedal activity.

    The robust finger and hypertrophied wrist and elbow bones indicate a strong grip and load bearing adaptations for the arms. The legs also show adaptations for load-bearing, especially at the hypertrophied knee joint. There was likely limited
    ankle loading, and the ankle would have had a hinge-like function, being most stable if positioned perpendicularly to the leg as opposed to at an angle in apes. Danuvius was likely able to achieve a strong grip with its big toes, unlike modern African
    great apes, which would have allowed it to grasp onto thinner trees. The limb proportions are most similar to those of bonobos.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Sat Nov 19 20:21:27 2022
    On Saturday, November 19, 2022 at 2:20:20 PM UTC-5, 69jp...@gmail.com wrote:
    On Sat, 19 Nov 2022 06:06:22 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Saturday, November 19, 2022 at 6:40:01 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 18 Nov 2022 03:45:32 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, November 18, 2022 at 2:12:32 AM UTC-5, 69jp...@gmail.com wrote:
    On Thu, 17 Nov 2022 15:53:51 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 12:57:57 PM UTC-5, 69jp...@gmail.com wrote:
    On Wed, 16 Nov 2022 22:42:03 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 1:29:04 AM UTC-5, Daud Deden wrote:
    On Wednesday, November 16, 2022 at 11:08:11 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 04 Nov 2022 02:21:55 -0400, jillery <69jp...@gmail.com>
    wrote:

    On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a
    Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.


    My impression is there isn't enough evidence to show whether Pliocene
    African apes descended from Miocene European apes or Miocene African
    apes. Either way, there was enough time between the two eras to have
    evolved differences between either Miocene populations and Pliocene S.
    tchadensis.

    I have recently become aware of:

    <https://en.wikipedia.org/wiki/Danuvius_guggenmosi>

    which was a Miocene European ape that may have evolved arboreal
    bipedalism similar to S.tchadensis.

    Depending on how widespread its range, and how successful its >> >> >> >> > descendants, it's plausible they lived south of the Black Sea during
    the late Miocene.

    The question then becomes whether it's more likely these apes found
    their way into Africa to become the ancestors of Pliocene
    S.tchadensis, or whether S.tchadensis evolved from Miocene African
    apes.

    Unfortunately, the habitat of these apes made their fossil
    preservation extremely rare, and so the evidence to well support
    either hypothesis is lacking.

    However, the question at least conditionally can be answered by
    comparing the likelihood of a migratory pathway during that time,
    versus the likelihood of arboreal bipedalism evolving independently in
    two populations.

    There are a number of anatomic features associated with arboreal
    bipedalism, some of which are necessary, ex. anterior foramen magnum,

    The foramen magnum is always situated relatively more anteriorly in immature than in mature apes.[ - and men. ]
    Not sure what you mean by "mature"; the individual or the species? >> >> >
    Individually.
    My understanding is the relative position of foramen magnum doesn't
    change significantly during human development.

    Right. In chimps the muzzle gradually moves anteriorly relative to the foramen magnum, in Homo only the nose does.
    Sorry, I erred above, I'd meant "...than in mature apes." The "and men" was NOT meant, I thought I'd erased it! Oops.
    The positions of the muzzle and/or nose relative to the foramen magnum
    don't inform bipedalism.

    It does, in tail-less upright orthogonal striding terrestrial former/partial arboreal bipeds, it does not in hopping bipeds.
    Cf short-faced giant kangaroo (short tail, striding upright bipedal)
    The topic isn't general bipedalism, but hominoid bipedalism.
    Topic: 'Human bipedalism'
    A version of hominoid bipedalism eg. Homo, hylobatid
    A version of primate bipedalism eg. Sifaka
    A version of mammal bipedalism eg. Kangaroo
    A version of animal bipedalism eg. Hoatzin (adult)

    Non-hominoid species don't inform this discussion.
    Either way, the important point is the position and angle of foramen
    magnum are diagnostic among all vertebrates for how they habitually >> >> >> hold their head, and so includes/excludes bipedalism among hominids.

    Yes, but no. Great apes are bipedal except when (hurrying) on open ground they adopt quadrupedalism. Homo retains the primitive bipedal gait of hominoid ancestors, as do hylobatids.
    All Homo species are great apes by definition, including H.sapiens.

    Yes, I meant 'arboreal great apes'. Humans are terrestrial great apes, hylobatids are arboreal lesser apes.

    They do/did quadrupedalism only in exceptional cases.

    https://youtu.be/pCrH6BOwxe4 15mph qpal running as a patas monkey, not a chimp.
    Imagine how much faster that person would be if he ran normally, like
    this:

    <https://www.youtube.com/watch?v=k3PZgbQ8auE>
    How is that an exceptional case among hominins? Only Usain Bolt can outrun qpal chimp at top speed.
    Your cited video shows an exceptional case among humans, which have relatively short arms and long legs, anatomically maladapted for
    quadrupedal locomotion. Also, even though his head is in extreme
    elevation, he can barely see where he's going, as his foramen magnum
    is anatomically maladapted for quadrupedal motion. Silly Guinness
    records notwithstanding, any human moving quadrupedally from a
    predator would soon become predator poop.
    and some of which are incidental, ex. molar patterns. Descendant
    populations are more likely to share these features than are >> >> >> >> > independent populations. This suggests to me that a sufficiently
    robust fossil record could answer this question with some degree of
    certainty.

    Alternately, my understanding is southern Europe and central Africa
    are ecological opposites, in the sense that when one is hot and dry
    the other is temperate and wet.
    Central Africa is and was hot,
    ... and wet aka tropical,

    The adoption of qpal knucklewalking by African apes indicates that their ancient habitat went through a dry phase (rainforest became patchy) forcing a terrestrial dog-like gait.
    Perhaps. My understanding is bipedal arboreal apes continued to walk >> >> bipedally on the ground, while non-bipedal arboreal apes also adopted >> >> quadrupedal habits on the ground.

    Bipedal walking is primitive in arboreal hominoids, quadrupedal walking is derived. I don't know of any 'non-bipedal arboreal apes', only monkeys.
    That's not my understanding. My understanding is chimpanzees,
    gorillas, and orangutans are non-bipedal arboreal apes, meaning when
    they are in the trees, they do not walk upright.

    Their body orientation on and under branches is primarily upright, not pronograde with all limbs in compression aka quadrupedal. The modern AMHs orthogonal posture is derived, not the same as primitive upright bipedal arboreal hominoids.
    You continue to use above a non-standard meaning of bipedalism.
    Hanging from branches using combinations of limbs isn't bipedalism any
    more than is climbing up coconut palms.
    As were most
    arboreal apes prior to Australopithecines.
    just right for the evolution of small bipedal arboreal apes.

    The fact that there are no small bipedal arboreal apes in Africa indicates that there was some climate shifting.
    Again perhaps. It also suggests small bipedal arboreal apes were
    outcompeted.

    They were, by monkeys which were more ground adapted, able to swiftly run between forest stands during a drier climate phase.

    the southern Black Sea is between temperate and tropical.
    Correct. Southern Europe and the Black Sea are at the same latitudes.
    This suggests they would tend to have the same climate. However, the
    Black Sea is farther inland, and so suffers more continental extremes.
    So any climate changes will appear first around the Black Sea and >> >> >> become more extreme compared to southern Europe.

    I'm talking about from 11ma through the MSC to 5ma. The Medit. & Red Seas dried out, the Black Sea didn't.
    The relative position of the Black Sea didn't change from then to now. >> >> The important point is its position is deep in Eurasia, where
    continental climates rule.

    It lies between the Atlantic-Mediterranean and the Caspian Sea, in the Peri-Tethyan basin, protected by the high Iranian plateau to the south. Not a typical continental climate.
    <https://www.britannica.com/place/Black-Sea/Climate>
    **********************************
    The climate of the landlocked Black Sea can be characterized generally
    as continental (i.e., subject to pronounced seasonal temperature
    variations), although climatic conditions in some parts of the basin
    are controlled to a great extent by the shoreline relief. A steppe
    climate, with cold winters and hot, dry summers, is found in the
    northwestern part of the basin exposed to the influence of air masses
    from the north.
    ************************************

    Summer in north including Bavaria via Danube valley, winter in south including visits further southwardly.
    I meant summer north of Black Sea...winter south of Black Sea

    I suppose Miocene apes collected frequent-flier miles.
    My understanding is the Mediterranean dried out only about 6mya, long >> >> after European, and presumably Black Sea, arboreal apes went extinct. >> >
    No, Danuvius and later Miocene apes there were of one lineage IMO, that may have lived there until 5ma, with successive expansional waves emigrating outwardly including towards Africa.

    The Red Sea is too far south to affect migration from Europe to Africa >> >> regardless of climate patterns.

    It is part of the African-Anatolian rift.
    I acknowledge that rift was one plausible pathway from Europe to
    Africa. The Red Sea was not, nor did it block such a pathway.

    I include it provisionally, more data needed.
    Sounds like a segue for aquatic ape hypothesis.
    Moving toward 30 degrees latitude, rainfall becomes seasonally dry, >> >> >> and then almost continuously dry. My understanding is, the only
    native forests south of the Caspian are in the mountains, and adjacent
    to the Mediterranean coasts. Arboreal apes of any kind would find >> >> >> these deserts impassible.

    You are speaking of recent climate. There are no arboreal apes there now.
    No, I am speaking of climate then *and* now. Regions around 30
    degrees latitude tend to be drier than those around the equator, with >> >> exceptions due to terrain and ocean currents.

    Stop temporarily.
    Unclear. Do you mean stop migration temporarily? If so, keep in mind
    that the same climate changes which would create arid conditions
    around 30 degrees latitude would also shrink forests further north and south.
    You appear to be claiming that the European Miocene apes could never have been linked to African and Asian apes. Yet they certainly were, else they wouldn't have existed at all.
    Such an "appearance" is incorrect. In certain cases, regions around
    30 degrees latitude have/had enough rainfall to support forests. The
    relevant point here is, global climate since the Miocene has gotten
    colder and drier, especially around 30 degrees latitude, which has led
    to the creation of large areas of treeless savannah and desert. I
    don't know when European and African forests separated. Do you?

    Not at the moment. However, gallery forests remained along rivers & lakes, and highlands tended to get precipitation after lowland plains dried. Apparently during the MSC the Red Sea was blocked from the Mediterranean and at some time (tectonically?)
    opened to the Indian Ocean. The post-MSC Zanclean flood may have refilled basins and brought moisture to the general Mediterranean region.

    Also, the question isn't about the origin of apes generally. It's
    about the origin of arboreal bipedal apes. We know they existed in
    Pliocene Africa. They *may* have existed in Miocene Europe. Even if
    they did, the two populations may still have evolved independently.
    To a first approximation, average rainfall and temperature are
    functions of latitude. However, while temperature is a function of >> >> >> the sine of latitude, rainfall is more complex. It tends to be
    continuously heavy near the equator, continuously dry near 30 degrees,
    and seasonally variable between 30 and 60 degrees. This general
    pattern is modified, sometimes dramatically, by terrain, ocean
    currents, seasons, and Milankovitch cycles.

    The most significant variable is Africa's northward tectonic
    migration, about a centimeter a year since before the Miocene. So, >> >> >> while central Africa has moved from south to north of the equator with
    little effect, north Africa has approached and then went north of 30
    degrees, making it over time ever drier, amplifying other climate >> >> >> trends, making once wooded areas into vast savannah and desert.

    Yes.

    Also, Africa's tectonic slide north almost certainly pinched closed >> >> >> the Gilbraltar Sttraits, which caused the Mediterranean to dry up at
    least once, and likely several times as sea levels rose and fell. The
    resulting hot salt basin would also have been impassible for arboreal
    apes.
    This is as true now as it was in the
    Miocene. This suggests to me there could not have been an unbroken
    forested path for arboreal apes to migrate between Europe/Near East
    and Central Africa.
    I would not claim nor disclaim that. The Levant is near the midpoint, extends the African Rift valley to Anatolia, is a major avian migration route between Africa and Eurasia, has fossil/artifacts of Homo erectus, neanderthal & sapiens
    oldest known cooking (fish .78ma) and earliest waternut gathering and bread making. The region is amenable to hominins & Homo.
    I acknowledge the facts you describe above. However, the Levant is >> >> >> savannah and desert except for a narrow strip along the Mediterranean
    and up in the mountains. While this is no problem for terrestrial >> >> >> bipeds like Homo, ISTM arboreal hominids like D.guggenmosi would have
    a much harder time living/migrating there.

    "is".
    Again, refer to microclimate of Levant 11ma - 5ma. Today's Dead Sea was once the vast brackish Lake Lisan that reached to Lebanon, a gallery forest may have reached from Anatolia to Egypt.
    The regions you describe above are part of the Mediterranean coastal >> >> mountains I mentioned previously.

    The Dead Sea is by no means a coastal mountain region.
    https://en.wikipedia.org/wiki/Judaean_Mountains

    These are part of a series of ranges all along the eastern
    Mediterranean coast.
    I agree a coastal Mediterranean
    forest is plausible.

    I'm referring to the tectonic rift valley between Zimbabwe/Zambia and Lebanon/Anatolia.
    ... which runs parallel to the Mediterranean coast.
    Of course, there were coastal forests as well, but they were affected by the MSC.

    However, my understanding is the evidence is
    insufficient to say if it would have been as extensive and continuous >> >> as you suggest during the time you suggest.

    Haven't got enough hard data yet.
    Cite the data you think is sufficient to answer this question.
    What is ISTM?


    It's shorthand acronym for "It Seems To Me"

    Ok, thanks.

    Danuvius, Rudapithecus, Graecopithecus, Oranopithecus each had a unique trait shared with hominins. I think of them as a superspecies with local variations.
    -
    If you place Danuvius half-way between fast brachiating bipedal long backed long achilles tendon hylobatids and bipedal Homo with long back and long achilles tendon, it fits perfectly.

    Wiki:
    Danuvius is thought to have had a broad chest. It is the first recorded Miocene great ape to have had the diaphragm located in the lower chest cavity, as in Homo, indicating an extended lower back and a greater number of functional lumbar
    vertebrae. This may have caused lordosis (the normal curvature of the human spine) and moved the center of mass over the hips and legs, which implies some habitual bipedal activity.

    The robust finger and hypertrophied wrist and elbow bones indicate a strong grip and load bearing adaptations for the arms. The legs also show adaptations for load-bearing, especially at the hypertrophied knee joint. There was likely limited
    ankle loading, and the ankle would have had a hinge-like function, being most stable if positioned perpendicularly to the leg as opposed to at an angle in apes. Danuvius was likely able to achieve a strong grip with its big toes, unlike modern African
    great apes, which would have allowed it to grasp onto thinner trees. The limb proportions are most similar to those of bonobos.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to daud.deden@gmail.com on Sun Nov 20 02:01:13 2022
    On Sat, 19 Nov 2022 12:43:27 -0800 (PST), Daud Deden
    <daud.deden@gmail.com> wrote:

    On Saturday, November 19, 2022 at 2:20:20 PM UTC-5, 69jp...@gmail.com wrote: >> On Sat, 19 Nov 2022 06:06:22 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Saturday, November 19, 2022 at 6:40:01 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 18 Nov 2022 03:45:32 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, November 18, 2022 at 2:12:32 AM UTC-5, 69jp...@gmail.com wrote:
    On Thu, 17 Nov 2022 15:53:51 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 12:57:57 PM UTC-5, 69jp...@gmail.com wrote:
    On Wed, 16 Nov 2022 22:42:03 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 1:29:04 AM UTC-5, Daud Deden wrote:
    On Wednesday, November 16, 2022 at 11:08:11 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 04 Nov 2022 02:21:55 -0400, jillery <69jp...@gmail.com>
    wrote:

    On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden >> >> >> >> >> > >>> >> <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a
    Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.


    My impression is there isn't enough evidence to show whether Pliocene
    African apes descended from Miocene European apes or Miocene African
    apes. Either way, there was enough time between the two eras to have
    evolved differences between either Miocene populations and Pliocene S.
    tchadensis.

    I have recently become aware of:

    <https://en.wikipedia.org/wiki/Danuvius_guggenmosi>

    which was a Miocene European ape that may have evolved arboreal
    bipedalism similar to S.tchadensis.

    Depending on how widespread its range, and how successful its >> >> >> >> >> > descendants, it's plausible they lived south of the Black Sea during
    the late Miocene.

    The question then becomes whether it's more likely these apes found
    their way into Africa to become the ancestors of Pliocene
    S.tchadensis, or whether S.tchadensis evolved from Miocene African
    apes.

    Unfortunately, the habitat of these apes made their fossil
    preservation extremely rare, and so the evidence to well support
    either hypothesis is lacking.

    However, the question at least conditionally can be answered by
    comparing the likelihood of a migratory pathway during that time,
    versus the likelihood of arboreal bipedalism evolving independently in
    two populations.

    There are a number of anatomic features associated with arboreal
    bipedalism, some of which are necessary, ex. anterior foramen magnum,

    The foramen magnum is always situated relatively more anteriorly in immature than in mature apes.[ - and men. ]
    Not sure what you mean by "mature"; the individual or the species? >> >> >> >
    Individually.
    My understanding is the relative position of foramen magnum doesn't >> >> >> change significantly during human development.

    Right. In chimps the muzzle gradually moves anteriorly relative to the foramen magnum, in Homo only the nose does.
    Sorry, I erred above, I'd meant "...than in mature apes." The "and men" was NOT meant, I thought I'd erased it! Oops.
    The positions of the muzzle and/or nose relative to the foramen magnum >> >> don't inform bipedalism.

    It does, in tail-less upright orthogonal striding terrestrial former/partial arboreal bipeds, it does not in hopping bipeds.
    Cf short-faced giant kangaroo (short tail, striding upright bipedal)
    The topic isn't general bipedalism, but hominoid bipedalism.
    Non-hominoid species don't inform this discussion.

    <inserted your reply in your later post>

    Topic: 'Human bipedalism'


    Fair point. To be precise, the topic is the *origin* of human
    bipedalism. But human bipedalism didn't originate in humans, but is
    derived from *hominoid* ancestors like australopiths or earlier.


    A version of hominoid bipedalism eg. Homo, hylobatid
    A version of primate bipedalism eg. Sifaka
    A version of mammal bipedalism eg. Kangaroo
    A version of animal bipedalism eg. Hoatzin (adult)

    A version of animal bipedalism eg. T.rex

    If you want to expand the discussion beyond the origins of human
    bipedalism, then don't limit yourself to bipedalism; include all
    animal locomotion, up to and including invertebrates. Good luck with
    that.

    If you want to make coherent and relevant points about the origin of
    human bipedalism, then constrain your comments to Homo species and
    their likely ancestors.


    Either way, the important point is the position and angle of foramen
    magnum are diagnostic among all vertebrates for how they habitually
    hold their head, and so includes/excludes bipedalism among hominids.

    Yes, but no. Great apes are bipedal except when (hurrying) on open ground they adopt quadrupedalism. Homo retains the primitive bipedal gait of hominoid ancestors, as do hylobatids.
    All Homo species are great apes by definition, including H.sapiens. >> >> >
    Yes, I meant 'arboreal great apes'. Humans are terrestrial great apes, hylobatids are arboreal lesser apes.

    They do/did quadrupedalism only in exceptional cases.

    https://youtu.be/pCrH6BOwxe4 15mph qpal running as a patas monkey, not a chimp.
    Imagine how much faster that person would be if he ran normally, like
    this:

    <https://www.youtube.com/watch?v=k3PZgbQ8auE>
    How is that an exceptional case among hominins? Only Usain Bolt can outrun qpal chimp at top speed.
    Your cited video shows an exceptional case among humans, which have
    relatively short arms and long legs, anatomically maladapted for
    quadrupedal locomotion.

    Humans are faster qpal palm-down sprinter and qpal endurance runner than any other hominoid.
    Patas monkey's arms are shorter than their legs: https://www.britannica.com/animal/patas-monkey

    Locomotor Anatomy and Behavior of Patas Monkeys (Erythrocebus patas) with Comparison to Vervet Monkeys (Cercopithecus aethiops)
    Adrienne L. Zihlman and Carol E. Underwood

    Additional article information

    Abstract
    Patas monkeys (Erythrocebus patas) living in African savanna woodlands and grassland habitats have a locomotor system that allows them to run fast, presumably to avoid predators. Long fore- and hindlimbs, long foot bones, short toes, and a digitigrade
    foot posture were proposed as anatomical correlates with speed. In addition to skeletal proportions, soft tissue and whole body proportions are important components of the locomotor system. To further distinguish patas anatomy from other Old World
    monkeys, a comparative study based on dissection of skin, muscle, and bone from complete individuals of patas and vervet monkeys (Cercopithecus aethiops) was undertaken. Analysis reveals that small adjustments in patas skeletal proportions, relative mass
    of limbs and tail, and specific muscle groups promote efficient sagittal limb motion. The ability to run fast is based on a locomotor system adapted for long distance walking. The patas' larger home range and longer daily range than those of
    vervets give them access to highly dispersed, nutritious foods, water, and sleeping trees. Furthermore, patas monkeys have physiological adaptations that enable them to tolerate and dissipate heat. These features all contribute to the distinct
    adaptation that is the patas monkeys' basis for survival in grassland and savanna woodland areas.


    Footraces between humans and patas monkeys are exceptional events.


    Also, even though his head is in extreme
    elevation, he can barely see where he's going, as his foramen magnum
    is anatomically maladapted for quadrupedal motion. Silly Guinness
    records notwithstanding, any human moving quadrupedally from a
    predator would soon become predator poop.

    Why? Carrying a blade pirate-style teeth-clenched, with a few pards similarly equipped, would present predators with a serious challenge. Bipedally, better weapons could be carried, of course, but running itself isn't enough. Patas, verbet & baboons
    climb trees, qpal running is just the short sprint to flight.


    Imagine yourself running quadrupedally with a blade pirate-style teeth clenched. Now imagine yourself running out of breath and exhausted as
    the predator you're running from catches up and eats you.

    Fun is fun, but at least make your jokes relevant to the topic.


    and some of which are incidental, ex. molar patterns. Descendant
    populations are more likely to share these features than are >> >> >> >> >> > independent populations. This suggests to me that a sufficiently
    robust fossil record could answer this question with some degree of
    certainty.

    Alternately, my understanding is southern Europe and central Africa
    are ecological opposites, in the sense that when one is hot and dry
    the other is temperate and wet.
    Central Africa is and was hot,
    ... and wet aka tropical,

    The adoption of qpal knucklewalking by African apes indicates that their ancient habitat went through a dry phase (rainforest became patchy) forcing a terrestrial dog-like gait.
    Perhaps. My understanding is bipedal arboreal apes continued to walk >> >> >> bipedally on the ground, while non-bipedal arboreal apes also adopted >> >> >> quadrupedal habits on the ground.

    Bipedal walking is primitive in arboreal hominoids, quadrupedal walking is derived. I don't know of any 'non-bipedal arboreal apes', only monkeys.
    That's not my understanding. My understanding is chimpanzees,
    gorillas, and orangutans are non-bipedal arboreal apes, meaning when
    they are in the trees, they do not walk upright.

    Their body orientation on and under branches is primarily upright, not pronograde with all limbs in compression aka quadrupedal. The modern AMHs orthogonal posture is derived, not the same as primitive upright bipedal arboreal hominoids.
    You continue to use above a non-standard meaning of bipedalism.

    Please direct me to "a standard meaning of bipedalism". Afaik, bipedalism is a trait of locomoting on 2 legs in compression, whether the hands are swinging, carrying or plucking.
    Sloths are quadrumanual, orangs are also called that when hanging tensionally from four limbs, but bipedal when walking on thick branches.


    I acknowledge I am no authority to assert a standard meaning of
    *human* bipedalism. But I rely on the list of diagnostic features as
    described by Erika's aka Gutsick Gibbon's, who is at least one
    authority. From the video you cited previously:

    <https://youtu.be/jo2ZLnucuHY>

    1. Foramen magnum and occipital condyles positioned anterior and
    angled vertically.

    2. Vertebrate lumbar lordosis.

    3. Bowl-shaped pelvis with sagittally oriented iliia and anterior
    iliac spine.

    4. Broad sacrum.

    5. Thick cortical bone around femur neck.

    6. Flattened elliptical distal condyles.

    7. Opterator externus groove.

    8. Valgus knee.

    9. Three arches of foot's sole.

    Also, I note that Erika expressed the same criticism I did about your quadrupedal human, that the foramen magnum precludes such habitual
    behavior.


    Hanging from branches using combinations of limbs isn't bipedalism any
    more than is climbing up coconut palms.

    Suspension itself is not bipedalism.


    That's what I said.


    As were most
    arboreal apes prior to Australopithecines.
    just right for the evolution of small bipedal arboreal apes.

    The fact that there are no small bipedal arboreal apes in Africa indicates that there was some climate shifting.
    Again perhaps. It also suggests small bipedal arboreal apes were
    outcompeted.

    They were, by monkeys which were more ground adapted, able to swiftly run between forest stands during a drier climate phase.

    the southern Black Sea is between temperate and tropical.
    Correct. Southern Europe and the Black Sea are at the same latitudes.
    This suggests they would tend to have the same climate. However, the
    Black Sea is farther inland, and so suffers more continental extremes.
    So any climate changes will appear first around the Black Sea and >> >> >> >> become more extreme compared to southern Europe.

    I'm talking about from 11ma through the MSC to 5ma. The Medit. & Red Seas dried out, the Black Sea didn't.
    The relative position of the Black Sea didn't change from then to now.
    The important point is its position is deep in Eurasia, where
    continental climates rule.

    It lies between the Atlantic-Mediterranean and the Caspian Sea, in the Peri-Tethyan basin, protected by the high Iranian plateau to the south. Not a typical continental climate.
    <https://www.britannica.com/place/Black-Sea/Climate>
    **********************************
    The climate of the landlocked Black Sea can be characterized generally >> >> as continental (i.e., subject to pronounced seasonal temperature
    variations), although climatic conditions in some parts of the basin
    are controlled to a great extent by the shoreline relief. A steppe
    climate, with cold winters and hot, dry summers, is found in the
    northwestern part of the basin exposed to the influence of air masses
    from the north.
    ************************************

    Summer in north including Bavaria via Danube valley, winter in south including visits further southwardly.
    I suppose Miocene apes collected frequent-flier miles.
    They weren't sessile, but very mobile.


    I am unaware of any arboreal species which seasonally migrate. To the
    best of my knowledge, although they may have a large home range, they
    stick to one area throughout the year. This would suggest migrating
    Miocene arboreal apes are a unique exception. Do you know of any
    extant arboreal animals which seasonally migrate?


    My understanding is the Mediterranean dried out only about 6mya, long >> >> >> after European, and presumably Black Sea, arboreal apes went extinct. >> >> >
    No, Danuvius and later Miocene apes there were of one lineage IMO, that may have lived there until 5ma, with successive expansional waves emigrating outwardly including towards Africa.

    The Red Sea is too far south to affect migration from Europe to Africa
    regardless of climate patterns.

    It is part of the African-Anatolian rift.
    I acknowledge that rift was one plausible pathway from Europe to
    Africa. The Red Sea was not, nor did it block such a pathway.

    I include it provisionally, more data needed.
    Sounds like a segue for aquatic ape hypothesis.

    Most proponents of that hypothesis tend to refuse to acknowledge that all extant (and by extension, archaic) Homo sleep well sheltered (dry, warm, shielded) from the elements (or try to be). Thus it is unrealistic imo.
    Of course, I refer to the surrounding region, which today is hyper-arid


    Moving toward 30 degrees latitude, rainfall becomes seasonally dry,
    and then almost continuously dry. My understanding is, the only
    native forests south of the Caspian are in the mountains, and adjacent
    to the Mediterranean coasts. Arboreal apes of any kind would find >> >> >> >> these deserts impassible.

    You are speaking of recent climate. There are no arboreal apes there now.
    No, I am speaking of climate then *and* now. Regions around 30
    degrees latitude tend to be drier than those around the equator, with >> >> >> exceptions due to terrain and ocean currents.
    Another stop.
    Stop temporarily.


    Ok, stop as in "be right back". But this isn't a real-time chat.
    What's the point of mentioning it?


    Unclear. Do you mean stop migration temporarily? If so, keep in mind
    that the same climate changes which would create arid conditions
    around 30 degrees latitude would also shrink forests further north and
    south.
    You appear to be claiming that the European Miocene apes could never have been linked to African and Asian apes. Yet they certainly were, else they wouldn't have existed at all.
    Such an "appearance" is incorrect. In certain cases, regions around
    30 degrees latitude have/had enough rainfall to support forests. The
    relevant point here is, global climate since the Miocene has gotten
    colder and drier, especially around 30 degrees latitude, which has led >> >> to the creation of large areas of treeless savannah and desert. I
    don't know when European and African forests separated. Do you?

    Also, the question isn't about the origin of apes generally. It's
    about the origin of arboreal bipedal apes. We know they existed in
    Pliocene Africa. They *may* have existed in Miocene Europe. Even if
    they did, the two populations may still have evolved independently.
    To a first approximation, average rainfall and temperature are
    functions of latitude. However, while temperature is a function of >> >> >> >> the sine of latitude, rainfall is more complex. It tends to be
    continuously heavy near the equator, continuously dry near 30 degrees,
    and seasonally variable between 30 and 60 degrees. This general
    pattern is modified, sometimes dramatically, by terrain, ocean
    currents, seasons, and Milankovitch cycles.

    The most significant variable is Africa's northward tectonic
    migration, about a centimeter a year since before the Miocene. So, >> >> >> >> while central Africa has moved from south to north of the equator with
    little effect, north Africa has approached and then went north of 30
    degrees, making it over time ever drier, amplifying other climate >> >> >> >> trends, making once wooded areas into vast savannah and desert.

    Yes.

    Also, Africa's tectonic slide north almost certainly pinched closed
    the Gilbraltar Sttraits, which caused the Mediterranean to dry up at
    least once, and likely several times as sea levels rose and fell. The
    resulting hot salt basin would also have been impassible for arboreal
    apes.
    This is as true now as it was in the
    Miocene. This suggests to me there could not have been an unbroken
    forested path for arboreal apes to migrate between Europe/Near East
    and Central Africa.
    I would not claim nor disclaim that. The Levant is near the midpoint, extends the African Rift valley to Anatolia, is a major avian migration route between Africa and Eurasia, has fossil/artifacts of Homo erectus, neanderthal & sapiens
    oldest known cooking (fish .78ma) and earliest waternut gathering and bread making. The region is amenable to hominins & Homo.
    I acknowledge the facts you describe above. However, the Levant is >> >> >> >> savannah and desert except for a narrow strip along the Mediterranean
    and up in the mountains. While this is no problem for terrestrial >> >> >> >> bipeds like Homo, ISTM arboreal hominids like D.guggenmosi would have
    a much harder time living/migrating there.

    "is".
    Again, refer to microclimate of Levant 11ma - 5ma. Today's Dead Sea was once the vast brackish Lake Lisan that reached to Lebanon, a gallery forest may have reached from Anatolia to Egypt.
    The regions you describe above are part of the Mediterranean coastal >> >> >> mountains I mentioned previously.

    The Dead Sea is by no means a coastal mountain region.
    https://en.wikipedia.org/wiki/Judaean_Mountains

    These are part of a series of ranges all along the eastern
    Mediterranean coast.
    I agree a coastal Mediterranean
    forest is plausible.

    I'm referring to the tectonic rift valley between Zimbabwe/Zambia and Lebanon/Anatolia.
    ... which runs parallel to the Mediterranean coast.
    Of course, there were coastal forests as well, but they were affected by the MSC.

    However, my understanding is the evidence is
    insufficient to say if it would have been as extensive and continuous >> >> >> as you suggest during the time you suggest.

    Haven't got enough hard data yet.
    Cite the data you think is sufficient to answer this question.
    What is ISTM?


    It's shorthand acronym for "It Seems To Me"

    Ok, thanks.

    Danuvius, Rudapithecus, Graecopithecus, Oranopithecus each had a unique trait shared with hominins. I think of them as a superspecies with local variations.
    -
    If you place Danuvius half-way between fast brachiating bipedal long backed long achilles tendon hylobatids and bipedal Homo with long back and long achilles tendon, it fits perfectly.

    Wiki:
    Danuvius is thought to have had a broad chest. It is the first recorded Miocene great ape to have had the diaphragm located in the lower chest cavity, as in Homo, indicating an extended lower back and a greater number of functional lumbar
    vertebrae. This may have caused lordosis (the normal curvature of the human spine) and moved the center of mass over the hips and legs, which implies some habitual bipedal activity.

    The robust finger and hypertrophied wrist and elbow bones indicate a strong grip and load bearing adaptations for the arms. The legs also show adaptations for load-bearing, especially at the hypertrophied knee joint. There was likely limited
    ankle loading, and the ankle would have had a hinge-like function, being most stable if positioned perpendicularly to the leg as opposed to at an angle in apes. Danuvius was likely able to achieve a strong grip with its big toes, unlike modern African
    great apes, which would have allowed it to grasp onto thinner trees. The limb proportions are most similar to those of bonobos.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Sun Nov 20 01:50:25 2022
    On Sunday, November 20, 2022 at 2:01:18 AM UTC-5, 69jp...@gmail.com wrote:
    On Sat, 19 Nov 2022 12:43:27 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Saturday, November 19, 2022 at 2:20:20 PM UTC-5, 69jp...@gmail.com wrote:
    On Sat, 19 Nov 2022 06:06:22 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Saturday, November 19, 2022 at 6:40:01 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 18 Nov 2022 03:45:32 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, November 18, 2022 at 2:12:32 AM UTC-5, 69jp...@gmail.com wrote:
    On Thu, 17 Nov 2022 15:53:51 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 12:57:57 PM UTC-5, 69jp...@gmail.com wrote:
    On Wed, 16 Nov 2022 22:42:03 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 1:29:04 AM UTC-5, Daud Deden wrote:
    On Wednesday, November 16, 2022 at 11:08:11 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 04 Nov 2022 02:21:55 -0400, jillery <69jp...@gmail.com>
    wrote:

    On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden >> >> >> >> >> > >>> >> <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a
    Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.


    My impression is there isn't enough evidence to show whether Pliocene
    African apes descended from Miocene European apes or Miocene African
    apes. Either way, there was enough time between the two eras to have
    evolved differences between either Miocene populations and Pliocene S.
    tchadensis.

    I have recently become aware of:

    <https://en.wikipedia.org/wiki/Danuvius_guggenmosi>

    which was a Miocene European ape that may have evolved arboreal
    bipedalism similar to S.tchadensis.

    Depending on how widespread its range, and how successful its
    descendants, it's plausible they lived south of the Black Sea during
    the late Miocene.

    The question then becomes whether it's more likely these apes found
    their way into Africa to become the ancestors of Pliocene >> >> >> >> >> > S.tchadensis, or whether S.tchadensis evolved from Miocene African
    apes.

    Unfortunately, the habitat of these apes made their fossil >> >> >> >> >> > preservation extremely rare, and so the evidence to well support
    either hypothesis is lacking.

    However, the question at least conditionally can be answered by
    comparing the likelihood of a migratory pathway during that time,
    versus the likelihood of arboreal bipedalism evolving independently in
    two populations.

    There are a number of anatomic features associated with arboreal
    bipedalism, some of which are necessary, ex. anterior foramen magnum,

    The foramen magnum is always situated relatively more anteriorly in immature than in mature apes.[ - and men. ]
    Not sure what you mean by "mature"; the individual or the species?

    Individually.
    My understanding is the relative position of foramen magnum doesn't >> >> >> change significantly during human development.

    Right. In chimps the muzzle gradually moves anteriorly relative to the foramen magnum, in Homo only the nose does.
    Sorry, I erred above, I'd meant "...than in mature apes." The "and men" was NOT meant, I thought I'd erased it! Oops.
    The positions of the muzzle and/or nose relative to the foramen magnum >> >> don't inform bipedalism.

    It does, in tail-less upright orthogonal striding terrestrial former/partial arboreal bipeds, it does not in hopping bipeds.
    Cf short-faced giant kangaroo (short tail, striding upright bipedal)
    The topic isn't general bipedalism, but hominoid bipedalism.
    Non-hominoid species don't inform this discussion.
    <inserted your reply in your later post>

    Topic: 'Human bipedalism'


    Fair point. To be precise, the topic is the *origin* of human
    bipedalism. But human bipedalism didn't originate in humans, but is
    derived from *hominoid* ancestors like australopiths or earlier.
    A version of hominoid bipedalism eg. Homo, hylobatid
    A version of primate bipedalism eg. Sifaka
    A version of mammal bipedalism eg. Kangaroo
    A version of animal bipedalism eg. Hoatzin (adult)
    A version of animal bipedalism eg. T.rex

    If you want to expand the discussion beyond the origins of human
    bipedalism, then don't limit yourself to bipedalism; include all
    animal locomotion, up to and including invertebrates. Good luck with
    that.
    If you want to make coherent and relevant points about the origin of
    human bipedalism, then constrain your comments to Homo species and
    their likely ancestors.

    That is a good way to lose useful information relative to the topic, IMO. You've just erased hylobatids from the conversation. Just like Lieberman did in his endurance running H. erectus fantasy.

    Adult chimps have protruding muzzles and are mostly qpal on the ground.
    Adult humans have flat faces and are bipedal on the ground.

    Either way, the important point is the position and angle of foramen
    magnum are diagnostic among all vertebrates for how they habitually
    hold their head, and so includes/excludes bipedalism among hominids.

    Yes, but no. Great apes are bipedal except when (hurrying) on open ground they adopt quadrupedalism. Homo retains the primitive bipedal gait of hominoid ancestors, as do hylobatids.
    All Homo species are great apes by definition, including H.sapiens. >> >> >
    Yes, I meant 'arboreal great apes'. Humans are terrestrial great apes, hylobatids are arboreal lesser apes.

    They do/did quadrupedalism only in exceptional cases.

    https://youtu.be/pCrH6BOwxe4 15mph qpal running as a patas monkey, not a chimp.
    Imagine how much faster that person would be if he ran normally, like >> >> this:

    <https://www.youtube.com/watch?v=k3PZgbQ8auE>
    How is that an exceptional case among hominins? Only Usain Bolt can outrun qpal chimp at top speed.
    Your cited video shows an exceptional case among humans, which have
    relatively short arms and long legs, anatomically maladapted for
    quadrupedal locomotion.

    Humans are faster qpal palm-down sprinter and qpal endurance runner than any other hominoid.
    Patas monkey's arms are shorter than their legs: https://www.britannica.com/animal/patas-monkey

    Locomotor Anatomy and Behavior of Patas Monkeys (Erythrocebus patas) with Comparison to Vervet Monkeys (Cercopithecus aethiops)
    Adrienne L. Zihlman and Carol E. Underwood

    Additional article information

    Abstract
    Patas monkeys (Erythrocebus patas) living in African savanna woodlands and grassland habitats have a locomotor system that allows them to run fast, presumably to avoid predators. Long fore- and hindlimbs, long foot bones, short toes, and a digitigrade
    foot posture were proposed as anatomical correlates with speed. In addition to skeletal proportions, soft tissue and whole body proportions are important components of the locomotor system. To further distinguish patas anatomy from other Old World
    monkeys, a comparative study based on dissection of skin, muscle, and bone from complete individuals of patas and vervet monkeys (Cercopithecus aethiops) was undertaken. Analysis reveals that small adjustments in patas skeletal proportions, relative mass
    of limbs and tail, and specific muscle groups promote efficient sagittal limb motion. The ability to run fast is based on a locomotor system adapted for long distance walking. The patas' larger home range and longer daily range than those of
    vervets give them access to highly dispersed, nutritious foods, water, and sleeping trees. Furthermore, patas monkeys have physiological adaptations that enable them to tolerate and dissipate heat. These features all contribute to the distinct
    adaptation that is the patas monkeys' basis for survival in grassland and savanna woodland areas.
    Footraces between humans and patas monkeys are exceptional events.
    Also, even though his head is in extreme
    elevation, he can barely see where he's going, as his foramen magnum
    is anatomically maladapted for quadrupedal motion. Silly Guinness
    records notwithstanding, any human moving quadrupedally from a
    predator would soon become predator poop.

    Why? Carrying a blade pirate-style teeth-clenched, with a few pards similarly equipped, would present predators with a serious challenge. Bipedally, better weapons could be carried, of course, but running itself isn't enough. Patas, vervet & baboons
    climb trees, qpal running is just the short sprint to flight.
    Imagine yourself running quadrupedally with a blade pirate-style teeth clenched. Now imagine yourself running out of breath and exhausted as
    the predator you're running from catches up and eats you.

    Don't bring a fang to a knife fight. Don't run with scissors. But most importantly, don't get encircled, because then you're prey. My pards and I run out only far enough to encircle said predator, then sing kumbaya as we slash it into ribbons of jerky.
    Predators attack from behind. There is no behind in a circle. But there is a vulnerable behind in an encircled predator. That is why the first knife slashes a rear hamstring/achilles/artery, while a pard is taunting up front, keeping the predator's
    attention away. Being quadrupedal with a knife is less useful than being bipedal with a knife. But it by no means is as vulnerable as being bipedal without one.

    Fun is fun, but at least make your jokes relevant to the topic.
    and some of which are incidental, ex. molar patterns. Descendant
    populations are more likely to share these features than are
    independent populations. This suggests to me that a sufficiently
    robust fossil record could answer this question with some degree of
    certainty.

    Alternately, my understanding is southern Europe and central Africa
    are ecological opposites, in the sense that when one is hot and dry
    the other is temperate and wet.
    Central Africa is and was hot,
    ... and wet aka tropical,

    The adoption of qpal knucklewalking by African apes indicates that their ancient habitat went through a dry phase (rainforest became patchy) forcing a terrestrial dog-like gait.
    Perhaps. My understanding is bipedal arboreal apes continued to walk
    bipedally on the ground, while non-bipedal arboreal apes also adopted
    quadrupedal habits on the ground.

    Bipedal walking is primitive in arboreal hominoids, quadrupedal walking is derived. I don't know of any 'non-bipedal arboreal apes', only monkeys.
    That's not my understanding. My understanding is chimpanzees,
    gorillas, and orangutans are non-bipedal arboreal apes, meaning when >> >> they are in the trees, they do not walk upright.

    Their body orientation on and under branches is primarily upright, not pronograde with all limbs in compression aka quadrupedal. The modern AMHs orthogonal posture is derived, not the same as primitive upright bipedal arboreal hominoids.
    You continue to use above a non-standard meaning of bipedalism.

    Please direct me to "a standard meaning of bipedalism". Afaik, bipedalism is a trait of locomoting on 2 legs in compression, whether the hands are swinging, carrying or plucking.
    Sloths are quadrumanual, orangs are also called that when hanging tensionally from four limbs, but bipedal when walking on thick branches.
    I acknowledge I am no authority to assert a standard meaning of
    *human* bipedalism. But I rely on the list of diagnostic features as described by Erika's aka Gutsick Gibbon's, who is at least one
    authority. From the video you cited previously:

    <https://youtu.be/jo2ZLnucuHY>

    1. Foramen magnum and occipital condyles positioned anterior and
    angled vertically.

    2. Vertebrate lumbar lordosis.

    3. Bowl-shaped pelvis with sagittally oriented iliia and anterior
    iliac spine.

    4. Broad sacrum.

    5. Thick cortical bone around femur neck.

    6. Flattened elliptical distal condyles.

    7. Opterator externus groove.

    8. Valgus knee.

    9. Three arches of foot's sole.

    Also, I note that Erika expressed the same criticism I did about your quadrupedal human, that the foramen magnum precludes such habitual
    behavior.

    Rather obvious that. Yet we can do it, quickly when we have to. Our body form is closer to monkeys than to apes in some ways.

    A list of features does not a meaning make.

    Please direct me to "a standard meaning of bipedalism". You demanded it, I requested it.
    Because there are some octopi that notoriously walk bipedally, they don't have any of those features.
    BUT THEY DO WALK ON TWO LIMBS IN COMPRESSION. And **THAT** is the standard meaning of bipedalism.
    So you must incorporate that into your description of human bipedalism. And so should Erika.

    Hanging from branches using combinations of limbs isn't bipedalism any
    more than is climbing up coconut palms.

    Suspension itself is not bipedalism.
    That's what I said.
    As were most
    arboreal apes prior to Australopithecines.
    just right for the evolution of small bipedal arboreal apes.

    The fact that there are no small bipedal arboreal apes in Africa indicates that there was some climate shifting.
    Again perhaps. It also suggests small bipedal arboreal apes were
    outcompeted.

    They were, by monkeys which were more ground adapted, able to swiftly run between forest stands during a drier climate phase.

    the southern Black Sea is between temperate and tropical.
    Correct. Southern Europe and the Black Sea are at the same latitudes.
    This suggests they would tend to have the same climate. However, the
    Black Sea is farther inland, and so suffers more continental extremes.
    So any climate changes will appear first around the Black Sea and
    become more extreme compared to southern Europe.

    I'm talking about from 11ma through the MSC to 5ma. The Medit. & Red Seas dried out, the Black Sea didn't.
    The relative position of the Black Sea didn't change from then to now.
    The important point is its position is deep in Eurasia, where
    continental climates rule.

    It lies between the Atlantic-Mediterranean and the Caspian Sea, in the Peri-Tethyan basin, protected by the high Iranian plateau to the south. Not a typical continental climate.
    <https://www.britannica.com/place/Black-Sea/Climate>
    **********************************
    The climate of the landlocked Black Sea can be characterized generally >> >> as continental (i.e., subject to pronounced seasonal temperature
    variations), although climatic conditions in some parts of the basin >> >> are controlled to a great extent by the shoreline relief. A steppe
    climate, with cold winters and hot, dry summers, is found in the
    northwestern part of the basin exposed to the influence of air masses >> >> from the north.
    ************************************

    Summer in north including Bavaria via Danube valley, winter in south including visits further southwardly.
    I suppose Miocene apes collected frequent-flier miles.
    They weren't sessile, but very mobile.
    I am unaware of any arboreal species which seasonally migrate.

    Songbirds? If you meant hominoids only, they are all tropical. Miocene apes had warm/cool seasons, they did migrate.

    To the
    best of my knowledge, although they may have a large home range, they
    stick to one area throughout the year. This would suggest migrating
    Miocene arboreal apes are a unique exception. Do you know of any
    extant arboreal animals which seasonally migrate?

    Songbirds? Which 'arboreal animals' do you mean, hominoids only?

    My understanding is the Mediterranean dried out only about 6mya, long
    after European, and presumably Black Sea, arboreal apes went extinct.

    No, Danuvius and later Miocene apes there were of one lineage IMO, that may have lived there until 5ma, with successive expansional waves emigrating outwardly including towards Africa.

    The Red Sea is too far south to affect migration from Europe to Africa
    regardless of climate patterns.

    It is part of the African-Anatolian rift.
    I acknowledge that rift was one plausible pathway from Europe to
    Africa. The Red Sea was not, nor did it block such a pathway.

    I include it provisionally, more data needed.
    Sounds like a segue for aquatic ape hypothesis.

    Most proponents of that hypothesis tend to refuse to acknowledge that all extant (and by extension, archaic) Homo sleep well sheltered (dry, warm, shielded) from the elements (or try to be). Thus it is unrealistic imo.
    Of course, I refer to the surrounding region, which today is hyper-arid


    Moving toward 30 degrees latitude, rainfall becomes seasonally dry,
    and then almost continuously dry. My understanding is, the only >> >> >> >> native forests south of the Caspian are in the mountains, and adjacent
    to the Mediterranean coasts. Arboreal apes of any kind would find
    these deserts impassible.

    You are speaking of recent climate. There are no arboreal apes there now.
    No, I am speaking of climate then *and* now. Regions around 30
    degrees latitude tend to be drier than those around the equator, with
    exceptions due to terrain and ocean currents.
    Another stop.
    Stop temporarily.
    Ok, stop as in "be right back". But this isn't a real-time chat.
    What's the point of mentioning it?
    To inform that I was stopping until i could get wifi again.

    Unclear. Do you mean stop migration temporarily? If so, keep in mind
    that the same climate changes which would create arid conditions
    around 30 degrees latitude would also shrink forests further north and
    south.
    You appear to be claiming that the European Miocene apes could never have been linked to African and Asian apes. Yet they certainly were, else they wouldn't have existed at all.
    Such an "appearance" is incorrect. In certain cases, regions around
    30 degrees latitude have/had enough rainfall to support forests. The >> >> relevant point here is, global climate since the Miocene has gotten
    colder and drier, especially around 30 degrees latitude, which has led >> >> to the creation of large areas of treeless savannah and desert. I
    don't know when European and African forests separated. Do you?

    Also, the question isn't about the origin of apes generally. It's
    about the origin of arboreal bipedal apes. We know they existed in
    Pliocene Africa. They *may* have existed in Miocene Europe. Even if
    they did, the two populations may still have evolved independently.
    To a first approximation, average rainfall and temperature are >> >> >> >> functions of latitude. However, while temperature is a function of
    the sine of latitude, rainfall is more complex. It tends to be >> >> >> >> continuously heavy near the equator, continuously dry near 30 degrees,
    and seasonally variable between 30 and 60 degrees. This general >> >> >> >> pattern is modified, sometimes dramatically, by terrain, ocean >> >> >> >> currents, seasons, and Milankovitch cycles.

    The most significant variable is Africa's northward tectonic
    migration, about a centimeter a year since before the Miocene. So,
    while central Africa has moved from south to north of the equator with
    little effect, north Africa has approached and then went north of 30
    degrees, making it over time ever drier, amplifying other climate
    trends, making once wooded areas into vast savannah and desert. >> >> >> >
    Yes.

    Also, Africa's tectonic slide north almost certainly pinched closed
    the Gilbraltar Sttraits, which caused the Mediterranean to dry up at
    least once, and likely several times as sea levels rose and fell. The
    resulting hot salt basin would also have been impassible for arboreal
    apes.
    This is as true now as it was in the
    Miocene. This suggests to me there could not have been an unbroken
    forested path for arboreal apes to migrate between Europe/Near East
    and Central Africa.
    I would not claim nor disclaim that. The Levant is near the midpoint, extends the African Rift valley to Anatolia, is a major avian migration route between Africa and Eurasia, has fossil/artifacts of Homo erectus, neanderthal & sapiens
    oldest known cooking (fish .78ma) and earliest waternut gathering and bread making. The region is amenable to hominins & Homo.
    I acknowledge the facts you describe above. However, the Levant is
    savannah and desert except for a narrow strip along the Mediterranean
    and up in the mountains. While this is no problem for terrestrial
    bipeds like Homo, ISTM arboreal hominids like D.guggenmosi would have
    a much harder time living/migrating there.

    "is".
    Again, refer to microclimate of Levant 11ma - 5ma. Today's Dead Sea was once the vast brackish Lake Lisan that reached to Lebanon, a gallery forest may have reached from Anatolia to Egypt.
    The regions you describe above are part of the Mediterranean coastal
    mountains I mentioned previously.

    The Dead Sea is by no means a coastal mountain region.
    https://en.wikipedia.org/wiki/Judaean_Mountains

    These are part of a series of ranges all along the eastern
    Mediterranean coast.
    I agree a coastal Mediterranean
    forest is plausible.

    I'm referring to the tectonic rift valley between Zimbabwe/Zambia and Lebanon/Anatolia.
    ... which runs parallel to the Mediterranean coast.
    Of course, there were coastal forests as well, but they were affected by the MSC.

    However, my understanding is the evidence is
    insufficient to say if it would have been as extensive and continuous
    as you suggest during the time you suggest.

    Haven't got enough hard data yet.
    Cite the data you think is sufficient to answer this question.
    What is ISTM?


    It's shorthand acronym for "It Seems To Me"

    Ok, thanks.

    Danuvius, Rudapithecus, Graecopithecus, Oranopithecus each had a unique trait shared with hominins. I think of them as a superspecies with local variations.
    -
    If you place Danuvius half-way between fast brachiating bipedal long backed long achilles tendon hylobatids and bipedal Homo with long back and long achilles tendon, it fits perfectly.

    Wiki:
    Danuvius is thought to have had a broad chest. It is the first recorded Miocene great ape to have had the diaphragm located in the lower chest cavity, as in Homo, indicating an extended lower back and a greater number of functional lumbar
    vertebrae. This may have caused lordosis (the normal curvature of the human spine) and moved the center of mass over the hips and legs, which implies some habitual bipedal activity.

    The robust finger and hypertrophied wrist and elbow bones indicate a strong grip and load bearing adaptations for the arms. The legs also show adaptations for load-bearing, especially at the hypertrophied knee joint. There was likely
    limited ankle loading, and the ankle would have had a hinge-like function, being most stable if positioned perpendicularly to the leg as opposed to at an angle in apes. Danuvius was likely able to achieve a strong grip with its big toes, unlike modern
    African great apes, which would have allowed it to grasp onto thinner trees. The limb proportions are most similar to those of bonobos.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to Daud Deden on Sun Nov 20 20:26:09 2022
    On Sunday, November 20, 2022 at 4:50:27 AM UTC-5, Daud Deden wrote:
    On Sunday, November 20, 2022 at 2:01:18 AM UTC-5, 69jp...@gmail.com wrote:
    On Sat, 19 Nov 2022 12:43:27 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Saturday, November 19, 2022 at 2:20:20 PM UTC-5, 69jp...@gmail.com wrote:
    On Sat, 19 Nov 2022 06:06:22 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Saturday, November 19, 2022 at 6:40:01 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 18 Nov 2022 03:45:32 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, November 18, 2022 at 2:12:32 AM UTC-5, 69jp...@gmail.com wrote:
    On Thu, 17 Nov 2022 15:53:51 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 12:57:57 PM UTC-5, 69jp...@gmail.com wrote:
    On Wed, 16 Nov 2022 22:42:03 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 1:29:04 AM UTC-5, Daud Deden wrote:
    On Wednesday, November 16, 2022 at 11:08:11 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 04 Nov 2022 02:21:55 -0400, jillery <69jp...@gmail.com>
    wrote:

    On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden >> >> >> >> >> > >>> <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE> >> >> >> >> >> > >>> >> >>
    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps> >> >> >> >> >> > >>> >> >>
    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a
    Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.


    My impression is there isn't enough evidence to show whether Pliocene
    African apes descended from Miocene European apes or Miocene African
    apes. Either way, there was enough time between the two eras to have
    evolved differences between either Miocene populations and Pliocene S.
    tchadensis.

    I have recently become aware of:

    <https://en.wikipedia.org/wiki/Danuvius_guggenmosi>

    which was a Miocene European ape that may have evolved arboreal
    bipedalism similar to S.tchadensis.

    Depending on how widespread its range, and how successful its
    descendants, it's plausible they lived south of the Black Sea during
    the late Miocene.

    The question then becomes whether it's more likely these apes found
    their way into Africa to become the ancestors of Pliocene >> >> >> >> >> > S.tchadensis, or whether S.tchadensis evolved from Miocene African
    apes.

    Unfortunately, the habitat of these apes made their fossil
    preservation extremely rare, and so the evidence to well support
    either hypothesis is lacking.

    However, the question at least conditionally can be answered by
    comparing the likelihood of a migratory pathway during that time,
    versus the likelihood of arboreal bipedalism evolving independently in
    two populations.

    There are a number of anatomic features associated with arboreal
    bipedalism, some of which are necessary, ex. anterior foramen magnum,

    The foramen magnum is always situated relatively more anteriorly in immature than in mature apes.[ - and men. ]
    Not sure what you mean by "mature"; the individual or the species?

    Individually.
    My understanding is the relative position of foramen magnum doesn't
    change significantly during human development.

    Right. In chimps the muzzle gradually moves anteriorly relative to the foramen magnum, in Homo only the nose does.
    Sorry, I erred above, I'd meant "...than in mature apes." The "and men" was NOT meant, I thought I'd erased it! Oops.
    The positions of the muzzle and/or nose relative to the foramen magnum
    don't inform bipedalism.

    It does, in tail-less upright orthogonal striding terrestrial former/partial arboreal bipeds, it does not in hopping bipeds.
    Cf short-faced giant kangaroo (short tail, striding upright bipedal) >> The topic isn't general bipedalism, but hominoid bipedalism.
    Non-hominoid species don't inform this discussion.
    <inserted your reply in your later post>

    Topic: 'Human bipedalism'


    Fair point. To be precise, the topic is the *origin* of human
    bipedalism. But human bipedalism didn't originate in humans, but is derived from *hominoid* ancestors like australopiths or earlier.
    A version of hominoid bipedalism eg. Homo, hylobatid
    A version of primate bipedalism eg. Sifaka
    A version of mammal bipedalism eg. Kangaroo
    A version of animal bipedalism eg. Hoatzin (adult)
    A version of animal bipedalism eg. T.rex

    If you want to expand the discussion beyond the origins of human bipedalism, then don't limit yourself to bipedalism; include all
    animal locomotion, up to and including invertebrates. Good luck with
    that.
    If you want to make coherent and relevant points about the origin of
    human bipedalism, then constrain your comments to Homo species and
    their likely ancestors.
    That is a good way to lose useful information relative to the topic, IMO. You've just erased hylobatids from the conversation. Just like Lieberman did in his endurance running H. erectus fantasy.

    Adult chimps have protruding muzzles and are mostly qpal on the ground. Adult humans have flat faces and are bipedal on the ground.
    Either way, the important point is the position and angle of foramen
    magnum are diagnostic among all vertebrates for how they habitually
    hold their head, and so includes/excludes bipedalism among hominids.

    Yes, but no. Great apes are bipedal except when (hurrying) on open ground they adopt quadrupedalism. Homo retains the primitive bipedal gait of hominoid ancestors, as do hylobatids.
    All Homo species are great apes by definition, including H.sapiens.

    Yes, I meant 'arboreal great apes'. Humans are terrestrial great apes, hylobatids are arboreal lesser apes.

    They do/did quadrupedalism only in exceptional cases.

    https://youtu.be/pCrH6BOwxe4 15mph qpal running as a patas monkey, not a chimp.
    Imagine how much faster that person would be if he ran normally, like
    this:

    <https://www.youtube.com/watch?v=k3PZgbQ8auE>
    How is that an exceptional case among hominins? Only Usain Bolt can outrun qpal chimp at top speed.
    Your cited video shows an exceptional case among humans, which have
    relatively short arms and long legs, anatomically maladapted for
    quadrupedal locomotion.

    Humans are faster qpal palm-down sprinter and qpal endurance runner than any other hominoid.
    Patas monkey's arms are shorter than their legs: https://www.britannica.com/animal/patas-monkey

    Locomotor Anatomy and Behavior of Patas Monkeys (Erythrocebus patas) with Comparison to Vervet Monkeys (Cercopithecus aethiops)
    Adrienne L. Zihlman and Carol E. Underwood

    Additional article information

    Abstract
    Patas monkeys (Erythrocebus patas) living in African savanna woodlands and grassland habitats have a locomotor system that allows them to run fast, presumably to avoid predators. Long fore- and hindlimbs, long foot bones, short toes, and a
    digitigrade foot posture were proposed as anatomical correlates with speed. In addition to skeletal proportions, soft tissue and whole body proportions are important components of the locomotor system. To further distinguish patas anatomy from other Old
    World monkeys, a comparative study based on dissection of skin, muscle, and bone from complete individuals of patas and vervet monkeys (Cercopithecus aethiops) was undertaken. Analysis reveals that small adjustments in patas skeletal proportions,
    relative mass of limbs and tail, and specific muscle groups promote efficient sagittal limb motion. The ability to run fast is based on a locomotor system adapted for long distance walking. The patas' larger home range and longer daily range than those
    of
    vervets give them access to highly dispersed, nutritious foods, water, and sleeping trees. Furthermore, patas monkeys have physiological adaptations that enable them to tolerate and dissipate heat. These features all contribute to the distinct
    adaptation that is the patas monkeys' basis for survival in grassland and savanna woodland areas.
    Footraces between humans and patas monkeys are exceptional events.
    Also, even though his head is in extreme
    elevation, he can barely see where he's going, as his foramen magnum
    is anatomically maladapted for quadrupedal motion. Silly Guinness
    records notwithstanding, any human moving quadrupedally from a
    predator would soon become predator poop.

    Why? Carrying a blade pirate-style teeth-clenched, with a few pards similarly equipped, would present predators with a serious challenge. Bipedally, better weapons could be carried, of course, but running itself isn't enough. Patas, vervet & baboons
    climb trees, qpal running is just the short sprint to flight.
    Imagine yourself running quadrupedally with a blade pirate-style teeth clenched. Now imagine yourself running out of breath and exhausted as
    the predator you're running from catches up and eats you.
    Don't bring a fang to a knife fight. Don't run with scissors. But most importantly, don't get encircled, because then you're prey. My pards and I run out only far enough to encircle said predator, then sing kumbaya as we slash it into ribbons of jerky.
    Predators attack from behind. There is no behind in a circle. But there is a vulnerable behind in an encircled predator. That is why the first knife slashes a rear hamstring/achilles/artery, while a pard is taunting up front, keeping the predator's
    attention away. Being quadrupedal with a knife is less useful than being bipedal with a knife. But it by no means is as vulnerable as being bipedal without one.
    Fun is fun, but at least make your jokes relevant to the topic.
    and some of which are incidental, ex. molar patterns. Descendant
    populations are more likely to share these features than are
    independent populations. This suggests to me that a sufficiently
    robust fossil record could answer this question with some degree of
    certainty.

    Alternately, my understanding is southern Europe and central Africa
    are ecological opposites, in the sense that when one is hot and dry
    the other is temperate and wet.
    Central Africa is and was hot,
    ... and wet aka tropical,

    The adoption of qpal knucklewalking by African apes indicates that their ancient habitat went through a dry phase (rainforest became patchy) forcing a terrestrial dog-like gait.
    Perhaps. My understanding is bipedal arboreal apes continued to walk
    bipedally on the ground, while non-bipedal arboreal apes also adopted
    quadrupedal habits on the ground.

    Bipedal walking is primitive in arboreal hominoids, quadrupedal walking is derived. I don't know of any 'non-bipedal arboreal apes', only monkeys.
    That's not my understanding. My understanding is chimpanzees,
    gorillas, and orangutans are non-bipedal arboreal apes, meaning when >> >> they are in the trees, they do not walk upright.

    Their body orientation on and under branches is primarily upright, not pronograde with all limbs in compression aka quadrupedal. The modern AMHs orthogonal posture is derived, not the same as primitive upright bipedal arboreal hominoids.
    You continue to use above a non-standard meaning of bipedalism.

    Please direct me to "a standard meaning of bipedalism". Afaik, bipedalism is a trait of locomoting on 2 legs in compression, whether the hands are swinging, carrying or plucking.
    Sloths are quadrumanual, orangs are also called that when hanging tensionally from four limbs, but bipedal when walking on thick branches.
    I acknowledge I am no authority to assert a standard meaning of
    *human* bipedalism. But I rely on the list of diagnostic features as described by Erika's aka Gutsick Gibbon's, who is at least one
    authority. From the video you cited previously:

    <https://youtu.be/jo2ZLnucuHY>

    1. Foramen magnum and occipital condyles positioned anterior and
    angled vertically.

    2. Vertebrate lumbar lordosis.

    3. Bowl-shaped pelvis with sagittally oriented iliia and anterior
    iliac spine.

    4. Broad sacrum.

    5. Thick cortical bone around femur neck.

    6. Flattened elliptical distal condyles.

    7. Opterator externus groove.

    8. Valgus knee.

    9. Three arches of foot's sole.

    Also, I note that Erika expressed the same criticism I did about your quadrupedal human, that the foramen magnum precludes such habitual behavior.
    Rather obvious that. Yet we can do it, quickly when we have to. Our body form is closer to monkeys than to apes in some ways.

    A list of features does not a meaning make.

    Please direct me to "a standard meaning of bipedalism". You demanded it, I requested it.
    Because there are some octopi that notoriously walk bipedally, they don't have any of those features.
    BUT THEY DO WALK ON TWO LIMBS IN COMPRESSION. And **THAT** is the standard meaning of bipedalism.
    So you must incorporate that into your description of human bipedalism. And so should Erika.
    Hanging from branches using combinations of limbs isn't bipedalism any >> more than is climbing up coconut palms.

    Suspension itself is not bipedalism.
    That's what I said.
    As were most
    arboreal apes prior to Australopithecines.
    just right for the evolution of small bipedal arboreal apes.

    The fact that there are no small bipedal arboreal apes in Africa indicates that there was some climate shifting.
    Again perhaps. It also suggests small bipedal arboreal apes were >> >> >> outcompeted.

    They were, by monkeys which were more ground adapted, able to swiftly run between forest stands during a drier climate phase.

    the southern Black Sea is between temperate and tropical.
    Correct. Southern Europe and the Black Sea are at the same latitudes.
    This suggests they would tend to have the same climate. However, the
    Black Sea is farther inland, and so suffers more continental extremes.
    So any climate changes will appear first around the Black Sea and
    become more extreme compared to southern Europe.

    I'm talking about from 11ma through the MSC to 5ma. The Medit. & Red Seas dried out, the Black Sea didn't.
    The relative position of the Black Sea didn't change from then to now.
    The important point is its position is deep in Eurasia, where
    continental climates rule.

    It lies between the Atlantic-Mediterranean and the Caspian Sea, in the Peri-Tethyan basin, protected by the high Iranian plateau to the south. Not a typical continental climate.
    <https://www.britannica.com/place/Black-Sea/Climate>
    **********************************
    The climate of the landlocked Black Sea can be characterized generally
    as continental (i.e., subject to pronounced seasonal temperature
    variations), although climatic conditions in some parts of the basin >> >> are controlled to a great extent by the shoreline relief. A steppe >> >> climate, with cold winters and hot, dry summers, is found in the
    northwestern part of the basin exposed to the influence of air masses
    from the north.
    ************************************

    Summer in north including Bavaria via Danube valley, winter in south including visits further southwardly.
    I suppose Miocene apes collected frequent-flier miles.
    They weren't sessile, but very mobile.
    I am unaware of any arboreal species which seasonally migrate.
    Songbirds? If you meant hominoids only, they are all tropical. Miocene apes had warm/cool seasons, they did migrate.
    To the
    best of my knowledge, although they may have a large home range, they stick to one area throughout the year. This would suggest migrating Miocene arboreal apes are a unique exception. Do you know of any
    extant arboreal animals which seasonally migrate?
    Songbirds? Which 'arboreal animals' do you mean, hominoids only?
    My understanding is the Mediterranean dried out only about 6mya, long
    after European, and presumably Black Sea, arboreal apes went extinct.

    No, Danuvius and later Miocene apes there were of one lineage IMO, that may have lived there until 5ma, with successive expansional waves emigrating outwardly including towards Africa.

    The Red Sea is too far south to affect migration from Europe to Africa
    regardless of climate patterns.

    It is part of the African-Anatolian rift.
    I acknowledge that rift was one plausible pathway from Europe to
    Africa. The Red Sea was not, nor did it block such a pathway.

    I include it provisionally, more data needed.
    Sounds like a segue for aquatic ape hypothesis.

    Most proponents of that hypothesis tend to refuse to acknowledge that all extant (and by extension, archaic) Homo sleep well sheltered (dry, warm, shielded) from the elements (or try to be). Thus it is unrealistic imo.
    Of course, I refer to the surrounding region, which today is hyper-arid


    Moving toward 30 degrees latitude, rainfall becomes seasonally dry,
    and then almost continuously dry. My understanding is, the only
    native forests south of the Caspian are in the mountains, and adjacent
    to the Mediterranean coasts. Arboreal apes of any kind would find
    these deserts impassible.

    You are speaking of recent climate. There are no arboreal apes there now.
    No, I am speaking of climate then *and* now. Regions around 30
    degrees latitude tend to be drier than those around the equator, with
    exceptions due to terrain and ocean currents.
    Another stop.
    Stop temporarily.
    Ok, stop as in "be right back". But this isn't a real-time chat.
    What's the point of mentioning it?
    To inform that I was stopping until i could get wifi again.
    Unclear. Do you mean stop migration temporarily? If so, keep in mind
    that the same climate changes which would create arid conditions
    around 30 degrees latitude would also shrink forests further north and >> south.
    You appear to be claiming that the European Miocene apes could never have been linked to African and Asian apes. Yet they certainly were, else they wouldn't have existed at all.
    Such an "appearance" is incorrect. In certain cases, regions around >> >> 30 degrees latitude have/had enough rainfall to support forests. The >> >> relevant point here is, global climate since the Miocene has gotten >> >> colder and drier, especially around 30 degrees latitude, which has led
    to the creation of large areas of treeless savannah and desert. I
    don't know when European and African forests separated. Do you?

    Also, the question isn't about the origin of apes generally. It's
    about the origin of arboreal bipedal apes. We know they existed in >> >> Pliocene Africa. They *may* have existed in Miocene Europe. Even if >> >> they did, the two populations may still have evolved independently. >> >> >> >> To a first approximation, average rainfall and temperature are >> >> >> >> functions of latitude. However, while temperature is a function of
    the sine of latitude, rainfall is more complex. It tends to be >> >> >> >> continuously heavy near the equator, continuously dry near 30 degrees,
    and seasonally variable between 30 and 60 degrees. This general
    pattern is modified, sometimes dramatically, by terrain, ocean >> >> >> >> currents, seasons, and Milankovitch cycles.

    The most significant variable is Africa's northward tectonic >> >> >> >> migration, about a centimeter a year since before the Miocene. So,
    while central Africa has moved from south to north of the equator with
    little effect, north Africa has approached and then went north of 30
    degrees, making it over time ever drier, amplifying other climate
    trends, making once wooded areas into vast savannah and desert.

    Yes.

    Also, Africa's tectonic slide north almost certainly pinched closed
    the Gilbraltar Sttraits, which caused the Mediterranean to dry up at
    least once, and likely several times as sea levels rose and fell. The
    resulting hot salt basin would also have been impassible for arboreal
    apes.
    This is as true now as it was in the
    Miocene. This suggests to me there could not have been an unbroken
    forested path for arboreal apes to migrate between Europe/Near East
    and Central Africa.
    I would not claim nor disclaim that. The Levant is near the midpoint, extends the African Rift valley to Anatolia, is a major avian migration route between Africa and Eurasia, has fossil/artifacts of Homo erectus, neanderthal & sapiens
    oldest known cooking (fish .78ma) and earliest waternut gathering and bread making. The region is amenable to hominins & Homo.
    I acknowledge the facts you describe above. However, the Levant is
    savannah and desert except for a narrow strip along the Mediterranean
    and up in the mountains. While this is no problem for terrestrial
    bipeds like Homo, ISTM arboreal hominids like D.guggenmosi would have
    a much harder time living/migrating there.

    "is".
    Again, refer to microclimate of Levant 11ma - 5ma. Today's Dead Sea was once the vast brackish Lake Lisan that reached to Lebanon, a gallery forest may have reached from Anatolia to Egypt.
    The regions you describe above are part of the Mediterranean coastal
    mountains I mentioned previously.

    The Dead Sea is by no means a coastal mountain region.
    https://en.wikipedia.org/wiki/Judaean_Mountains

    These are part of a series of ranges all along the eastern
    Mediterranean coast.
    I agree a coastal Mediterranean
    forest is plausible.

    I'm referring to the tectonic rift valley between Zimbabwe/Zambia and Lebanon/Anatolia.
    ... which runs parallel to the Mediterranean coast.
    Of course, there were coastal forests as well, but they were affected by the MSC.

    However, my understanding is the evidence is
    insufficient to say if it would have been as extensive and continuous
    as you suggest during the time you suggest.

    Haven't got enough hard data yet.
    Cite the data you think is sufficient to answer this question.
    What is ISTM?


    It's shorthand acronym for "It Seems To Me"

    Ok, thanks.

    Danuvius, Rudapithecus, Graecopithecus, Oranopithecus each had a unique trait shared with hominins. I think of them as a superspecies with local variations.
    -
    If you place Danuvius half-way between fast brachiating bipedal long backed long achilles tendon hylobatids and bipedal Homo with long back and long achilles tendon, it fits perfectly.

    Wiki:
    Danuvius is thought to have had a broad chest. It is the first recorded Miocene great ape to have had the diaphragm located in the lower chest cavity, as in Homo, indicating an extended lower back and a greater number of functional
    lumbar vertebrae. This may have caused lordosis (the normal curvature of the human spine) and moved the center of mass over the hips and legs, which implies some habitual bipedal activity.

    The robust finger and hypertrophied wrist and elbow bones indicate a strong grip and load bearing adaptations for the arms. The legs also show adaptations for load-bearing, especially at the hypertrophied knee joint. There was likely
    limited ankle loading, and the ankle would have had a hinge-like function, being most stable if positioned perpendicularly to the leg as opposed to at an angle in apes. Danuvius was likely able to achieve a strong grip with its big toes, unlike modern
    African great apes, which would have allowed it to grasp onto thinner trees. The limb proportions are most similar to those of bonobos.
    ---
    Q: Alex, what is Sifaka?

    The Origins of Bipedal Locomotion
    William EH Harcourt-Smith 2013
    Handbook of PA doi 10.1007/978-3-642-27800-6_48-3

    "BPism is a highly specialized & unusual form of primate locomotion, found today only in modern Hs."

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to daud.deden@gmail.com on Mon Nov 21 00:25:10 2022
    On Sun, 20 Nov 2022 01:50:25 -0800 (PST), Daud Deden
    <daud.deden@gmail.com> wrote:

    On Sunday, November 20, 2022 at 2:01:18 AM UTC-5, 69jp...@gmail.com wrote:
    On Sat, 19 Nov 2022 12:43:27 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Saturday, November 19, 2022 at 2:20:20 PM UTC-5, 69jp...@gmail.com wrote:
    On Sat, 19 Nov 2022 06:06:22 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Saturday, November 19, 2022 at 6:40:01 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 18 Nov 2022 03:45:32 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, November 18, 2022 at 2:12:32 AM UTC-5, 69jp...@gmail.com wrote:
    On Thu, 17 Nov 2022 15:53:51 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 12:57:57 PM UTC-5, 69jp...@gmail.com wrote:
    On Wed, 16 Nov 2022 22:42:03 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 1:29:04 AM UTC-5, Daud Deden wrote:
    On Wednesday, November 16, 2022 at 11:08:11 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 04 Nov 2022 02:21:55 -0400, jillery <69jp...@gmail.com>
    wrote:

    On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a
    Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.


    My impression is there isn't enough evidence to show whether Pliocene
    African apes descended from Miocene European apes or Miocene African
    apes. Either way, there was enough time between the two eras to have
    evolved differences between either Miocene populations and Pliocene S.
    tchadensis.

    I have recently become aware of:

    <https://en.wikipedia.org/wiki/Danuvius_guggenmosi>

    which was a Miocene European ape that may have evolved arboreal
    bipedalism similar to S.tchadensis.

    Depending on how widespread its range, and how successful its
    descendants, it's plausible they lived south of the Black Sea during
    the late Miocene.

    The question then becomes whether it's more likely these apes found
    their way into Africa to become the ancestors of Pliocene >> >> >> >> >> >> > S.tchadensis, or whether S.tchadensis evolved from Miocene African
    apes.

    Unfortunately, the habitat of these apes made their fossil >> >> >> >> >> >> > preservation extremely rare, and so the evidence to well support
    either hypothesis is lacking.

    However, the question at least conditionally can be answered by
    comparing the likelihood of a migratory pathway during that time,
    versus the likelihood of arboreal bipedalism evolving independently in
    two populations.

    There are a number of anatomic features associated with arboreal
    bipedalism, some of which are necessary, ex. anterior foramen magnum,

    The foramen magnum is always situated relatively more anteriorly in immature than in mature apes.[ - and men. ]
    Not sure what you mean by "mature"; the individual or the species?

    Individually.
    My understanding is the relative position of foramen magnum doesn't
    change significantly during human development.

    Right. In chimps the muzzle gradually moves anteriorly relative to the foramen magnum, in Homo only the nose does.
    Sorry, I erred above, I'd meant "...than in mature apes." The "and men" was NOT meant, I thought I'd erased it! Oops.
    The positions of the muzzle and/or nose relative to the foramen magnum
    don't inform bipedalism.

    It does, in tail-less upright orthogonal striding terrestrial former/partial arboreal bipeds, it does not in hopping bipeds.
    Cf short-faced giant kangaroo (short tail, striding upright bipedal)
    The topic isn't general bipedalism, but hominoid bipedalism.
    Non-hominoid species don't inform this discussion.
    <inserted your reply in your later post>

    Topic: 'Human bipedalism'


    Fair point. To be precise, the topic is the *origin* of human
    bipedalism. But human bipedalism didn't originate in humans, but is
    derived from *hominoid* ancestors like australopiths or earlier.
    A version of hominoid bipedalism eg. Homo, hylobatid
    A version of primate bipedalism eg. Sifaka
    A version of mammal bipedalism eg. Kangaroo
    A version of animal bipedalism eg. Hoatzin (adult)
    A version of animal bipedalism eg. T.rex

    If you want to expand the discussion beyond the origins of human
    bipedalism, then don't limit yourself to bipedalism; include all
    animal locomotion, up to and including invertebrates. Good luck with
    that.
    If you want to make coherent and relevant points about the origin of
    human bipedalism, then constrain your comments to Homo species and
    their likely ancestors.

    That is a good way to lose useful information relative to the topic, IMO. You've just erased hylobatids from the conversation. Just like Lieberman did in his endurance running H. erectus fantasy.


    The posts in this topic show how useful information is lost by being
    obscured with tangential topics. This is not to say those other
    topics aren't interesting. This is not to say that meandering and
    open-ended discussions aren't interesting. This is to say that IMO
    the topic of the origin of human bipedalism is interesting in itself.
    I hope you will join me in continuing to discuss that topic.


    Adult chimps have protruding muzzles and are mostly qpal on the ground.
    Adult humans have flat faces and are bipedal on the ground.

    Either way, the important point is the position and angle of foramen
    magnum are diagnostic among all vertebrates for how they habitually
    hold their head, and so includes/excludes bipedalism among hominids.

    Yes, but no. Great apes are bipedal except when (hurrying) on open ground they adopt quadrupedalism. Homo retains the primitive bipedal gait of hominoid ancestors, as do hylobatids.
    All Homo species are great apes by definition, including H.sapiens.

    Yes, I meant 'arboreal great apes'. Humans are terrestrial great apes, hylobatids are arboreal lesser apes.

    They do/did quadrupedalism only in exceptional cases.

    https://youtu.be/pCrH6BOwxe4 15mph qpal running as a patas monkey, not a chimp.
    Imagine how much faster that person would be if he ran normally, like >> >> >> this:

    <https://www.youtube.com/watch?v=k3PZgbQ8auE>
    How is that an exceptional case among hominins? Only Usain Bolt can outrun qpal chimp at top speed.
    Your cited video shows an exceptional case among humans, which have
    relatively short arms and long legs, anatomically maladapted for
    quadrupedal locomotion.

    Humans are faster qpal palm-down sprinter and qpal endurance runner than any other hominoid.
    Patas monkey's arms are shorter than their legs: https://www.britannica.com/animal/patas-monkey

    Locomotor Anatomy and Behavior of Patas Monkeys (Erythrocebus patas) with Comparison to Vervet Monkeys (Cercopithecus aethiops)
    Adrienne L. Zihlman and Carol E. Underwood

    Additional article information

    Abstract
    Patas monkeys (Erythrocebus patas) living in African savanna woodlands and grassland habitats have a locomotor system that allows them to run fast, presumably to avoid predators. Long fore- and hindlimbs, long foot bones, short toes, and a
    digitigrade foot posture were proposed as anatomical correlates with speed. In addition to skeletal proportions, soft tissue and whole body proportions are important components of the locomotor system. To further distinguish patas anatomy from other Old
    World monkeys, a comparative study based on dissection of skin, muscle, and bone from complete individuals of patas and vervet monkeys (Cercopithecus aethiops) was undertaken. Analysis reveals that small adjustments in patas skeletal proportions,
    relative mass of limbs and tail, and specific muscle groups promote efficient sagittal limb motion. The ability to run fast is based on a locomotor system adapted for long distance walking. The patas' larger home range and longer daily range than those
    of
    vervets give them access to highly dispersed, nutritious foods, water, and sleeping trees. Furthermore, patas monkeys have physiological adaptations that enable them to tolerate and dissipate heat. These features all contribute to the distinct
    adaptation that is the patas monkeys' basis for survival in grassland and savanna woodland areas.
    Footraces between humans and patas monkeys are exceptional events.
    Also, even though his head is in extreme
    elevation, he can barely see where he's going, as his foramen magnum
    is anatomically maladapted for quadrupedal motion. Silly Guinness
    records notwithstanding, any human moving quadrupedally from a
    predator would soon become predator poop.

    Why? Carrying a blade pirate-style teeth-clenched, with a few pards similarly equipped, would present predators with a serious challenge. Bipedally, better weapons could be carried, of course, but running itself isn't enough. Patas, vervet & baboons
    climb trees, qpal running is just the short sprint to flight.
    Imagine yourself running quadrupedally with a blade pirate-style teeth
    clenched. Now imagine yourself running out of breath and exhausted as
    the predator you're running from catches up and eats you.

    Don't bring a fang to a knife fight. Don't run with scissors. But most importantly, don't get encircled, because then you're prey. My pards and I run out only far enough to encircle said predator, then sing kumbaya as we slash it into ribbons of jerky.
    Predators attack from behind. There is no behind in a circle. But there is a vulnerable behind in an encircled predator. That is why the first knife slashes a rear hamstring/achilles/artery, while a pard is taunting up front, keeping the predator's
    attention away. Being quadrupedal with a knife is less useful than being bipedal with a knife. But it by no means is as vulnerable as being bipedal without one.

    Fun is fun, but at least make your jokes relevant to the topic.
    and some of which are incidental, ex. molar patterns. Descendant
    populations are more likely to share these features than are
    independent populations. This suggests to me that a sufficiently
    robust fossil record could answer this question with some degree of
    certainty.

    Alternately, my understanding is southern Europe and central Africa
    are ecological opposites, in the sense that when one is hot and dry
    the other is temperate and wet.
    Central Africa is and was hot,
    ... and wet aka tropical,

    The adoption of qpal knucklewalking by African apes indicates that their ancient habitat went through a dry phase (rainforest became patchy) forcing a terrestrial dog-like gait.
    Perhaps. My understanding is bipedal arboreal apes continued to walk
    bipedally on the ground, while non-bipedal arboreal apes also adopted
    quadrupedal habits on the ground.

    Bipedal walking is primitive in arboreal hominoids, quadrupedal walking is derived. I don't know of any 'non-bipedal arboreal apes', only monkeys.
    That's not my understanding. My understanding is chimpanzees,
    gorillas, and orangutans are non-bipedal arboreal apes, meaning when >> >> >> they are in the trees, they do not walk upright.

    Their body orientation on and under branches is primarily upright, not pronograde with all limbs in compression aka quadrupedal. The modern AMHs orthogonal posture is derived, not the same as primitive upright bipedal arboreal hominoids.
    You continue to use above a non-standard meaning of bipedalism.

    Please direct me to "a standard meaning of bipedalism". Afaik, bipedalism is a trait of locomoting on 2 legs in compression, whether the hands are swinging, carrying or plucking.
    Sloths are quadrumanual, orangs are also called that when hanging tensionally from four limbs, but bipedal when walking on thick branches.
    I acknowledge I am no authority to assert a standard meaning of
    *human* bipedalism. But I rely on the list of diagnostic features as
    described by Erika's aka Gutsick Gibbon's, who is at least one
    authority. From the video you cited previously:

    <https://youtu.be/jo2ZLnucuHY>

    1. Foramen magnum and occipital condyles positioned anterior and
    angled vertically.

    2. Vertebrate lumbar lordosis.

    3. Bowl-shaped pelvis with sagittally oriented iliia and anterior
    iliac spine.

    4. Broad sacrum.

    5. Thick cortical bone around femur neck.

    6. Flattened elliptical distal condyles.

    7. Opterator externus groove.

    8. Valgus knee.

    9. Three arches of foot's sole.

    Also, I note that Erika expressed the same criticism I did about your
    quadrupedal human, that the foramen magnum precludes such habitual
    behavior.

    Rather obvious that. Yet we can do it, quickly when we have to. Our body form is closer to monkeys than to apes in some ways.

    A list of features does not a meaning make.

    Please direct me to "a standard meaning of bipedalism". You demanded it, I requested it.
    Because there are some octopi that notoriously walk bipedally, they don't have any of those features.
    BUT THEY DO WALK ON TWO LIMBS IN COMPRESSION. And **THAT** is the standard meaning of bipedalism.
    So you must incorporate that into your description of human bipedalism. And so should Erika.

    Hanging from branches using combinations of limbs isn't bipedalism any >> >> more than is climbing up coconut palms.

    Suspension itself is not bipedalism.
    That's what I said.
    As were most
    arboreal apes prior to Australopithecines.
    just right for the evolution of small bipedal arboreal apes.

    The fact that there are no small bipedal arboreal apes in Africa indicates that there was some climate shifting.
    Again perhaps. It also suggests small bipedal arboreal apes were >> >> >> >> outcompeted.

    They were, by monkeys which were more ground adapted, able to swiftly run between forest stands during a drier climate phase.

    the southern Black Sea is between temperate and tropical.
    Correct. Southern Europe and the Black Sea are at the same latitudes.
    This suggests they would tend to have the same climate. However, the
    Black Sea is farther inland, and so suffers more continental extremes.
    So any climate changes will appear first around the Black Sea and
    become more extreme compared to southern Europe.

    I'm talking about from 11ma through the MSC to 5ma. The Medit. & Red Seas dried out, the Black Sea didn't.
    The relative position of the Black Sea didn't change from then to now.
    The important point is its position is deep in Eurasia, where
    continental climates rule.

    It lies between the Atlantic-Mediterranean and the Caspian Sea, in the Peri-Tethyan basin, protected by the high Iranian plateau to the south. Not a typical continental climate.
    <https://www.britannica.com/place/Black-Sea/Climate>
    **********************************
    The climate of the landlocked Black Sea can be characterized generally
    as continental (i.e., subject to pronounced seasonal temperature
    variations), although climatic conditions in some parts of the basin >> >> >> are controlled to a great extent by the shoreline relief. A steppe
    climate, with cold winters and hot, dry summers, is found in the
    northwestern part of the basin exposed to the influence of air masses >> >> >> from the north.
    ************************************

    Summer in north including Bavaria via Danube valley, winter in south including visits further southwardly.
    I suppose Miocene apes collected frequent-flier miles.
    They weren't sessile, but very mobile.
    I am unaware of any arboreal species which seasonally migrate.

    Songbirds? If you meant hominoids only, they are all tropical. Miocene apes had warm/cool seasons, they did migrate.

    To the
    best of my knowledge, although they may have a large home range, they
    stick to one area throughout the year. This would suggest migrating
    Miocene arboreal apes are a unique exception. Do you know of any
    extant arboreal animals which seasonally migrate?

    Songbirds? Which 'arboreal animals' do you mean, hominoids only?

    My understanding is the Mediterranean dried out only about 6mya, long
    after European, and presumably Black Sea, arboreal apes went extinct.

    No, Danuvius and later Miocene apes there were of one lineage IMO, that may have lived there until 5ma, with successive expansional waves emigrating outwardly including towards Africa.

    The Red Sea is too far south to affect migration from Europe to Africa
    regardless of climate patterns.

    It is part of the African-Anatolian rift.
    I acknowledge that rift was one plausible pathway from Europe to
    Africa. The Red Sea was not, nor did it block such a pathway.

    I include it provisionally, more data needed.
    Sounds like a segue for aquatic ape hypothesis.

    Most proponents of that hypothesis tend to refuse to acknowledge that all extant (and by extension, archaic) Homo sleep well sheltered (dry, warm, shielded) from the elements (or try to be). Thus it is unrealistic imo.
    Of course, I refer to the surrounding region, which today is hyper-arid


    Moving toward 30 degrees latitude, rainfall becomes seasonally dry,
    and then almost continuously dry. My understanding is, the only >> >> >> >> >> native forests south of the Caspian are in the mountains, and adjacent
    to the Mediterranean coasts. Arboreal apes of any kind would find
    these deserts impassible.

    You are speaking of recent climate. There are no arboreal apes there now.
    No, I am speaking of climate then *and* now. Regions around 30
    degrees latitude tend to be drier than those around the equator, with
    exceptions due to terrain and ocean currents.
    Another stop.
    Stop temporarily.
    Ok, stop as in "be right back". But this isn't a real-time chat.
    What's the point of mentioning it?
    To inform that I was stopping until i could get wifi again.

    Unclear. Do you mean stop migration temporarily? If so, keep in mind
    that the same climate changes which would create arid conditions
    around 30 degrees latitude would also shrink forests further north and >> >> south.
    You appear to be claiming that the European Miocene apes could never have been linked to African and Asian apes. Yet they certainly were, else they wouldn't have existed at all.
    Such an "appearance" is incorrect. In certain cases, regions around >> >> >> 30 degrees latitude have/had enough rainfall to support forests. The >> >> >> relevant point here is, global climate since the Miocene has gotten >> >> >> colder and drier, especially around 30 degrees latitude, which has led
    to the creation of large areas of treeless savannah and desert. I
    don't know when European and African forests separated. Do you?

    Also, the question isn't about the origin of apes generally. It's
    about the origin of arboreal bipedal apes. We know they existed in
    Pliocene Africa. They *may* have existed in Miocene Europe. Even if >> >> >> they did, the two populations may still have evolved independently. >> >> >> >> >> To a first approximation, average rainfall and temperature are >> >> >> >> >> functions of latitude. However, while temperature is a function of
    the sine of latitude, rainfall is more complex. It tends to be >> >> >> >> >> continuously heavy near the equator, continuously dry near 30 degrees,
    and seasonally variable between 30 and 60 degrees. This general >> >> >> >> >> pattern is modified, sometimes dramatically, by terrain, ocean >> >> >> >> >> currents, seasons, and Milankovitch cycles.

    The most significant variable is Africa's northward tectonic
    migration, about a centimeter a year since before the Miocene. So,
    while central Africa has moved from south to north of the equator with
    little effect, north Africa has approached and then went north of 30
    degrees, making it over time ever drier, amplifying other climate
    trends, making once wooded areas into vast savannah and desert. >> >> >> >> >
    Yes.

    Also, Africa's tectonic slide north almost certainly pinched closed
    the Gilbraltar Sttraits, which caused the Mediterranean to dry up at
    least once, and likely several times as sea levels rose and fell. The
    resulting hot salt basin would also have been impassible for arboreal
    apes.
    This is as true now as it was in the
    Miocene. This suggests to me there could not have been an unbroken
    forested path for arboreal apes to migrate between Europe/Near East
    and Central Africa.
    I would not claim nor disclaim that. The Levant is near the midpoint, extends the African Rift valley to Anatolia, is a major avian migration route between Africa and Eurasia, has fossil/artifacts of Homo erectus, neanderthal & sapiens
    oldest known cooking (fish .78ma) and earliest waternut gathering and bread making. The region is amenable to hominins & Homo.
    I acknowledge the facts you describe above. However, the Levant is
    savannah and desert except for a narrow strip along the Mediterranean
    and up in the mountains. While this is no problem for terrestrial
    bipeds like Homo, ISTM arboreal hominids like D.guggenmosi would have
    a much harder time living/migrating there.

    "is".
    Again, refer to microclimate of Levant 11ma - 5ma. Today's Dead Sea was once the vast brackish Lake Lisan that reached to Lebanon, a gallery forest may have reached from Anatolia to Egypt.
    The regions you describe above are part of the Mediterranean coastal
    mountains I mentioned previously.

    The Dead Sea is by no means a coastal mountain region.
    https://en.wikipedia.org/wiki/Judaean_Mountains

    These are part of a series of ranges all along the eastern
    Mediterranean coast.
    I agree a coastal Mediterranean
    forest is plausible.

    I'm referring to the tectonic rift valley between Zimbabwe/Zambia and Lebanon/Anatolia.
    ... which runs parallel to the Mediterranean coast.
    Of course, there were coastal forests as well, but they were affected by the MSC.

    However, my understanding is the evidence is
    insufficient to say if it would have been as extensive and continuous
    as you suggest during the time you suggest.

    Haven't got enough hard data yet.
    Cite the data you think is sufficient to answer this question.
    What is ISTM?


    It's shorthand acronym for "It Seems To Me"

    Ok, thanks.

    Danuvius, Rudapithecus, Graecopithecus, Oranopithecus each had a unique trait shared with hominins. I think of them as a superspecies with local variations.
    -
    If you place Danuvius half-way between fast brachiating bipedal long backed long achilles tendon hylobatids and bipedal Homo with long back and long achilles tendon, it fits perfectly.

    Wiki:
    Danuvius is thought to have had a broad chest. It is the first recorded Miocene great ape to have had the diaphragm located in the lower chest cavity, as in Homo, indicating an extended lower back and a greater number of functional lumbar
    vertebrae. This may have caused lordosis (the normal curvature of the human spine) and moved the center of mass over the hips and legs, which implies some habitual bipedal activity.

    The robust finger and hypertrophied wrist and elbow bones indicate a strong grip and load bearing adaptations for the arms. The legs also show adaptations for load-bearing, especially at the hypertrophied knee joint. There was likely
    limited ankle loading, and the ankle would have had a hinge-like function, being most stable if positioned perpendicularly to the leg as opposed to at an angle in apes. Danuvius was likely able to achieve a strong grip with its big toes, unlike modern
    African great apes, which would have allowed it to grasp onto thinner trees. The limb proportions are most similar to those of bonobos.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Mon Nov 21 00:31:25 2022
    On Monday, November 21, 2022 at 12:25:13 AM UTC-5, 69jp...@gmail.com wrote:
    On Sun, 20 Nov 2022 01:50:25 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Sunday, November 20, 2022 at 2:01:18 AM UTC-5, 69jp...@gmail.com wrote: >> On Sat, 19 Nov 2022 12:43:27 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Saturday, November 19, 2022 at 2:20:20 PM UTC-5, 69jp...@gmail.com wrote:
    On Sat, 19 Nov 2022 06:06:22 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Saturday, November 19, 2022 at 6:40:01 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 18 Nov 2022 03:45:32 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, November 18, 2022 at 2:12:32 AM UTC-5, 69jp...@gmail.com wrote:
    On Thu, 17 Nov 2022 15:53:51 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 12:57:57 PM UTC-5, 69jp...@gmail.com wrote:
    On Wed, 16 Nov 2022 22:42:03 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 1:29:04 AM UTC-5, Daud Deden wrote:
    On Wednesday, November 16, 2022 at 11:08:11 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 04 Nov 2022 02:21:55 -0400, jillery <69jp...@gmail.com>
    wrote:

    On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden >> >> >> >> >> >> > >>> <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE> >> >> >> >> >> >> > >>> >> >>
    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps> >> >> >> >> >> >> > >>> >> >>
    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a
    Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.


    My impression is there isn't enough evidence to show whether Pliocene
    African apes descended from Miocene European apes or Miocene African
    apes. Either way, there was enough time between the two eras to have
    evolved differences between either Miocene populations and Pliocene S.
    tchadensis.

    I have recently become aware of:

    <https://en.wikipedia.org/wiki/Danuvius_guggenmosi>

    which was a Miocene European ape that may have evolved arboreal
    bipedalism similar to S.tchadensis.

    Depending on how widespread its range, and how successful its
    descendants, it's plausible they lived south of the Black Sea during
    the late Miocene.

    The question then becomes whether it's more likely these apes found
    their way into Africa to become the ancestors of Pliocene
    S.tchadensis, or whether S.tchadensis evolved from Miocene African
    apes.

    Unfortunately, the habitat of these apes made their fossil
    preservation extremely rare, and so the evidence to well support
    either hypothesis is lacking.

    However, the question at least conditionally can be answered by
    comparing the likelihood of a migratory pathway during that time,
    versus the likelihood of arboreal bipedalism evolving independently in
    two populations.

    There are a number of anatomic features associated with arboreal
    bipedalism, some of which are necessary, ex. anterior foramen magnum,

    The foramen magnum is always situated relatively more anteriorly in immature than in mature apes.[ - and men. ]
    Not sure what you mean by "mature"; the individual or the species?

    Individually.
    My understanding is the relative position of foramen magnum doesn't
    change significantly during human development.

    Right. In chimps the muzzle gradually moves anteriorly relative to the foramen magnum, in Homo only the nose does.
    Sorry, I erred above, I'd meant "...than in mature apes." The "and men" was NOT meant, I thought I'd erased it! Oops.
    The positions of the muzzle and/or nose relative to the foramen magnum
    don't inform bipedalism.

    It does, in tail-less upright orthogonal striding terrestrial former/partial arboreal bipeds, it does not in hopping bipeds.
    Cf short-faced giant kangaroo (short tail, striding upright bipedal) >> >> The topic isn't general bipedalism, but hominoid bipedalism.
    Non-hominoid species don't inform this discussion.
    <inserted your reply in your later post>

    Topic: 'Human bipedalism'


    Fair point. To be precise, the topic is the *origin* of human
    bipedalism. But human bipedalism didn't originate in humans, but is
    derived from *hominoid* ancestors like australopiths or earlier.
    A version of hominoid bipedalism eg. Homo, hylobatid
    A version of primate bipedalism eg. Sifaka
    A version of mammal bipedalism eg. Kangaroo
    A version of animal bipedalism eg. Hoatzin (adult)
    A version of animal bipedalism eg. T.rex

    If you want to expand the discussion beyond the origins of human
    bipedalism, then don't limit yourself to bipedalism; include all
    animal locomotion, up to and including invertebrates. Good luck with
    that.
    If you want to make coherent and relevant points about the origin of
    human bipedalism, then constrain your comments to Homo species and
    their likely ancestors.

    That is a good way to lose useful information relative to the topic, IMO. You've just erased hylobatids from the conversation. Just like Lieberman did in his endurance running H. erectus fantasy.
    The posts in this topic show how useful information is lost by being obscured with tangential topics. This is not to say those other
    topics aren't interesting. This is not to say that meandering and
    open-ended discussions aren't interesting. This is to say that IMO
    the topic of the origin of human bipedalism is interesting in itself.
    I hope you will join me in continuing to discuss that topic.
    Adult chimps have protruding muzzles and are mostly qpal on the ground. >Adult humans have flat faces and are bipedal on the ground.

    Either way, the important point is the position and angle of foramen
    magnum are diagnostic among all vertebrates for how they habitually
    hold their head, and so includes/excludes bipedalism among hominids.

    Yes, but no. Great apes are bipedal except when (hurrying) on open ground they adopt quadrupedalism. Homo retains the primitive bipedal gait of hominoid ancestors, as do hylobatids.
    All Homo species are great apes by definition, including H.sapiens.

    Yes, I meant 'arboreal great apes'. Humans are terrestrial great apes, hylobatids are arboreal lesser apes.

    They do/did quadrupedalism only in exceptional cases.

    https://youtu.be/pCrH6BOwxe4 15mph qpal running as a patas monkey, not a chimp.
    Imagine how much faster that person would be if he ran normally, like
    this:

    <https://www.youtube.com/watch?v=k3PZgbQ8auE>
    How is that an exceptional case among hominins? Only Usain Bolt can outrun qpal chimp at top speed.
    Your cited video shows an exceptional case among humans, which have
    relatively short arms and long legs, anatomically maladapted for
    quadrupedal locomotion.

    Humans are faster qpal palm-down sprinter and qpal endurance runner than any other hominoid.
    Patas monkey's arms are shorter than their legs: https://www.britannica.com/animal/patas-monkey

    Locomotor Anatomy and Behavior of Patas Monkeys (Erythrocebus patas) with Comparison to Vervet Monkeys (Cercopithecus aethiops)
    Adrienne L. Zihlman and Carol E. Underwood

    Additional article information

    Abstract
    Patas monkeys (Erythrocebus patas) living in African savanna woodlands and grassland habitats have a locomotor system that allows them to run fast, presumably to avoid predators. Long fore- and hindlimbs, long foot bones, short toes, and a
    digitigrade foot posture were proposed as anatomical correlates with speed. In addition to skeletal proportions, soft tissue and whole body proportions are important components of the locomotor system. To further distinguish patas anatomy from other Old
    World monkeys, a comparative study based on dissection of skin, muscle, and bone from complete individuals of patas and vervet monkeys (Cercopithecus aethiops) was undertaken. Analysis reveals that small adjustments in patas skeletal proportions,
    relative mass of limbs and tail, and specific muscle groups promote efficient sagittal limb motion. The ability to run fast is based on a locomotor system adapted for long distance walking. The patas' larger home range and longer daily range than those
    of
    vervets give them access to highly dispersed, nutritious foods, water, and sleeping trees. Furthermore, patas monkeys have physiological adaptations that enable them to tolerate and dissipate heat. These features all contribute to the distinct
    adaptation that is the patas monkeys' basis for survival in grassland and savanna woodland areas.
    Footraces between humans and patas monkeys are exceptional events.
    Also, even though his head is in extreme
    elevation, he can barely see where he's going, as his foramen magnum >> >> is anatomically maladapted for quadrupedal motion. Silly Guinness
    records notwithstanding, any human moving quadrupedally from a
    predator would soon become predator poop.

    Why? Carrying a blade pirate-style teeth-clenched, with a few pards similarly equipped, would present predators with a serious challenge. Bipedally, better weapons could be carried, of course, but running itself isn't enough. Patas, vervet &
    baboons climb trees, qpal running is just the short sprint to flight.
    Imagine yourself running quadrupedally with a blade pirate-style teeth
    clenched. Now imagine yourself running out of breath and exhausted as
    the predator you're running from catches up and eats you.

    Don't bring a fang to a knife fight. Don't run with scissors. But most importantly, don't get encircled, because then you're prey. My pards and I run out only far enough to encircle said predator, then sing kumbaya as we slash it into ribbons of jerky.
    Predators attack from behind. There is no behind in a circle. But there is a vulnerable behind in an encircled predator. That is why the first knife slashes a rear hamstring/achilles/artery, while a pard is taunting up front, keeping the predator's
    attention away. Being quadrupedal with a knife is less useful than being bipedal with a knife. But it by no means is as vulnerable as being bipedal without one.

    Fun is fun, but at least make your jokes relevant to the topic.
    and some of which are incidental, ex. molar patterns. Descendant
    populations are more likely to share these features than are
    independent populations. This suggests to me that a sufficiently
    robust fossil record could answer this question with some degree of
    certainty.

    Alternately, my understanding is southern Europe and central Africa
    are ecological opposites, in the sense that when one is hot and dry
    the other is temperate and wet.
    Central Africa is and was hot,
    ... and wet aka tropical,

    The adoption of qpal knucklewalking by African apes indicates that their ancient habitat went through a dry phase (rainforest became patchy) forcing a terrestrial dog-like gait.
    Perhaps. My understanding is bipedal arboreal apes continued to walk
    bipedally on the ground, while non-bipedal arboreal apes also adopted
    quadrupedal habits on the ground.

    Bipedal walking is primitive in arboreal hominoids, quadrupedal walking is derived. I don't know of any 'non-bipedal arboreal apes', only monkeys.
    That's not my understanding. My understanding is chimpanzees,
    gorillas, and orangutans are non-bipedal arboreal apes, meaning when
    they are in the trees, they do not walk upright.

    Their body orientation on and under branches is primarily upright, not pronograde with all limbs in compression aka quadrupedal. The modern AMHs orthogonal posture is derived, not the same as primitive upright bipedal arboreal hominoids.
    You continue to use above a non-standard meaning of bipedalism.

    Please direct me to "a standard meaning of bipedalism". Afaik, bipedalism is a trait of locomoting on 2 legs in compression, whether the hands are swinging, carrying or plucking.
    Sloths are quadrumanual, orangs are also called that when hanging tensionally from four limbs, but bipedal when walking on thick branches.
    I acknowledge I am no authority to assert a standard meaning of
    *human* bipedalism. But I rely on the list of diagnostic features as
    described by Erika's aka Gutsick Gibbon's, who is at least one
    authority. From the video you cited previously:

    <https://youtu.be/jo2ZLnucuHY>

    1. Foramen magnum and occipital condyles positioned anterior and
    angled vertically.

    2. Vertebrate lumbar lordosis.

    3. Bowl-shaped pelvis with sagittally oriented iliia and anterior
    iliac spine.

    4. Broad sacrum.

    5. Thick cortical bone around femur neck.

    6. Flattened elliptical distal condyles.

    7. Opterator externus groove.

    8. Valgus knee.

    9. Three arches of foot's sole.

    Also, I note that Erika expressed the same criticism I did about your
    quadrupedal human, that the foramen magnum precludes such habitual
    behavior.

    Rather obvious that. Yet we can do it, quickly when we have to. Our body form is closer to monkeys than to apes in some ways.

    A list of features does not a meaning make.

    Please direct me to "a standard meaning of bipedalism". You demanded it, I requested it.
    Because there are some octopi that notoriously walk bipedally, they don't have any of those features.
    BUT THEY DO WALK ON TWO LIMBS IN COMPRESSION. And **THAT** is the standard meaning of bipedalism.
    So you must incorporate that into your description of human bipedalism. And so should Erika.

    Hanging from branches using combinations of limbs isn't bipedalism any >> >> more than is climbing up coconut palms.

    Suspension itself is not bipedalism.
    That's what I said.
    As were most
    arboreal apes prior to Australopithecines.
    just right for the evolution of small bipedal arboreal apes. >> >> >> >> >
    The fact that there are no small bipedal arboreal apes in Africa indicates that there was some climate shifting.
    Again perhaps. It also suggests small bipedal arboreal apes were >> >> >> >> outcompeted.

    They were, by monkeys which were more ground adapted, able to swiftly run between forest stands during a drier climate phase.

    the southern Black Sea is between temperate and tropical. >> >> >> >> >> Correct. Southern Europe and the Black Sea are at the same latitudes.
    This suggests they would tend to have the same climate. However, the
    Black Sea is farther inland, and so suffers more continental extremes.
    So any climate changes will appear first around the Black Sea and
    become more extreme compared to southern Europe.

    I'm talking about from 11ma through the MSC to 5ma. The Medit. & Red Seas dried out, the Black Sea didn't.
    The relative position of the Black Sea didn't change from then to now.
    The important point is its position is deep in Eurasia, where
    continental climates rule.

    It lies between the Atlantic-Mediterranean and the Caspian Sea, in the Peri-Tethyan basin, protected by the high Iranian plateau to the south. Not a typical continental climate.
    <https://www.britannica.com/place/Black-Sea/Climate>
    **********************************
    The climate of the landlocked Black Sea can be characterized generally
    as continental (i.e., subject to pronounced seasonal temperature
    variations), although climatic conditions in some parts of the basin
    are controlled to a great extent by the shoreline relief. A steppe >> >> >> climate, with cold winters and hot, dry summers, is found in the
    northwestern part of the basin exposed to the influence of air masses
    from the north.
    ************************************

    Summer in north including Bavaria via Danube valley, winter in south including visits further southwardly.
    I suppose Miocene apes collected frequent-flier miles.
    They weren't sessile, but very mobile.
    I am unaware of any arboreal species which seasonally migrate.

    Songbirds? If you meant hominoids only, they are all tropical. Miocene apes had warm/cool seasons, they did migrate.

    To the
    best of my knowledge, although they may have a large home range, they
    stick to one area throughout the year. This would suggest migrating
    Miocene arboreal apes are a unique exception. Do you know of any
    extant arboreal animals which seasonally migrate?

    Songbirds? Which 'arboreal animals' do you mean, hominoids only?

    My understanding is the Mediterranean dried out only about 6mya, long
    after European, and presumably Black Sea, arboreal apes went extinct.

    No, Danuvius and later Miocene apes there were of one lineage IMO, that may have lived there until 5ma, with successive expansional waves emigrating outwardly including towards Africa.

    The Red Sea is too far south to affect migration from Europe to Africa
    regardless of climate patterns.

    It is part of the African-Anatolian rift.
    I acknowledge that rift was one plausible pathway from Europe to
    Africa. The Red Sea was not, nor did it block such a pathway.

    I include it provisionally, more data needed.
    Sounds like a segue for aquatic ape hypothesis.

    Most proponents of that hypothesis tend to refuse to acknowledge that all extant (and by extension, archaic) Homo sleep well sheltered (dry, warm, shielded) from the elements (or try to be). Thus it is unrealistic imo.
    Of course, I refer to the surrounding region, which today is hyper-arid >> >

    Moving toward 30 degrees latitude, rainfall becomes seasonally dry,
    and then almost continuously dry. My understanding is, the only
    native forests south of the Caspian are in the mountains, and adjacent
    to the Mediterranean coasts. Arboreal apes of any kind would find
    these deserts impassible.

    You are speaking of recent climate. There are no arboreal apes there now.
    No, I am speaking of climate then *and* now. Regions around 30 >> >> >> >> degrees latitude tend to be drier than those around the equator, with
    exceptions due to terrain and ocean currents.
    Another stop.
    Stop temporarily.
    Ok, stop as in "be right back". But this isn't a real-time chat.
    What's the point of mentioning it?
    To inform that I was stopping until i could get wifi again.

    Unclear. Do you mean stop migration temporarily? If so, keep in mind >> >> that the same climate changes which would create arid conditions
    around 30 degrees latitude would also shrink forests further north and >> >> south.
    You appear to be claiming that the European Miocene apes could never have been linked to African and Asian apes. Yet they certainly were, else they wouldn't have existed at all.
    Such an "appearance" is incorrect. In certain cases, regions around >> >> >> 30 degrees latitude have/had enough rainfall to support forests. The
    relevant point here is, global climate since the Miocene has gotten >> >> >> colder and drier, especially around 30 degrees latitude, which has led
    to the creation of large areas of treeless savannah and desert. I >> >> >> don't know when European and African forests separated. Do you?

    Also, the question isn't about the origin of apes generally. It's >> >> >> about the origin of arboreal bipedal apes. We know they existed in >> >> >> Pliocene Africa. They *may* have existed in Miocene Europe. Even if >> >> >> they did, the two populations may still have evolved independently. >> >> >> >> >> To a first approximation, average rainfall and temperature are
    functions of latitude. However, while temperature is a function of
    the sine of latitude, rainfall is more complex. It tends to be
    continuously heavy near the equator, continuously dry near 30 degrees,
    and seasonally variable between 30 and 60 degrees. This general
    pattern is modified, sometimes dramatically, by terrain, ocean
    currents, seasons, and Milankovitch cycles.

    The most significant variable is Africa's northward tectonic >> >> >> >> >> migration, about a centimeter a year since before the Miocene. So,
    while central Africa has moved from south to north of the equator with
    little effect, north Africa has approached and then went north of 30
    degrees, making it over time ever drier, amplifying other climate
    trends, making once wooded areas into vast savannah and desert.

    Yes.

    Also, Africa's tectonic slide north almost certainly pinched closed
    the Gilbraltar Sttraits, which caused the Mediterranean to dry up at
    least once, and likely several times as sea levels rose and fell. The
    resulting hot salt basin would also have been impassible for arboreal
    apes.
    This is as true now as it was in the
    Miocene. This suggests to me there could not have been an unbroken
    forested path for arboreal apes to migrate between Europe/Near East
    and Central Africa.
    I would not claim nor disclaim that. The Levant is near the midpoint, extends the African Rift valley to Anatolia, is a major avian migration route between Africa and Eurasia, has fossil/artifacts of Homo erectus, neanderthal &
    sapiens oldest known cooking (fish .78ma) and earliest waternut gathering and bread making. The region is amenable to hominins & Homo.
    I acknowledge the facts you describe above. However, the Levant is
    savannah and desert except for a narrow strip along the Mediterranean
    and up in the mountains. While this is no problem for terrestrial
    bipeds like Homo, ISTM arboreal hominids like D.guggenmosi would have
    a much harder time living/migrating there.

    "is".
    Again, refer to microclimate of Levant 11ma - 5ma. Today's Dead Sea was once the vast brackish Lake Lisan that reached to Lebanon, a gallery forest may have reached from Anatolia to Egypt.
    The regions you describe above are part of the Mediterranean coastal
    mountains I mentioned previously.

    The Dead Sea is by no means a coastal mountain region.
    https://en.wikipedia.org/wiki/Judaean_Mountains

    These are part of a series of ranges all along the eastern
    Mediterranean coast.
    I agree a coastal Mediterranean
    forest is plausible.

    I'm referring to the tectonic rift valley between Zimbabwe/Zambia and Lebanon/Anatolia.
    ... which runs parallel to the Mediterranean coast.
    Of course, there were coastal forests as well, but they were affected by the MSC.

    However, my understanding is the evidence is
    insufficient to say if it would have been as extensive and continuous
    as you suggest during the time you suggest.

    Haven't got enough hard data yet.
    Cite the data you think is sufficient to answer this question.
    What is ISTM?


    It's shorthand acronym for "It Seems To Me"

    Ok, thanks.

    Danuvius, Rudapithecus, Graecopithecus, Oranopithecus each had a unique trait shared with hominins. I think of them as a superspecies with local variations.
    -
    If you place Danuvius half-way between fast brachiating bipedal long backed long achilles tendon hylobatids and bipedal Homo with long back and long achilles tendon, it fits perfectly.

    Wiki:
    Danuvius is thought to have had a broad chest. It is the first recorded Miocene great ape to have had the diaphragm located in the lower chest cavity, as in Homo, indicating an extended lower back and a greater number of functional
    lumbar vertebrae. This may have caused lordosis (the normal curvature of the human spine) and moved the center of mass over the hips and legs, which implies some habitual bipedal activity.

    The robust finger and hypertrophied wrist and elbow bones indicate a strong grip and load bearing adaptations for the arms. The legs also show adaptations for load-bearing, especially at the hypertrophied knee joint. There was likely
    limited ankle loading, and the ankle would have had a hinge-like function, being most stable if positioned perpendicularly to the leg as opposed to at an angle in apes. Danuvius was likely able to achieve a strong grip with its big toes, unlike modern
    African great apes, which would have allowed it to grasp onto thinner trees. The limb proportions are most similar to those of bonobos.

    So far, you have offered up a 'parts list' of human bipedalism features, in response to my request for "a standard meaning of bipedalism". A list of features does not a meaning make, in my experience. In all of my conversations with others about Biology *
    or* Engineering, I have never heard of a list of parts being referred to as a "standard meaning of" anything. A "standard measure" perhaps, but not a standard meaning.
    Perhaps Erika will inform what the 'standard meaning of bipedalism' is, since you rely on her authority, in addition to the parts list. But I can't see how to improve the simple statement given, "two limbs in compression", when applied to whichever the
    animate taxon under discussion.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to daud.deden@gmail.com on Mon Nov 21 06:44:37 2022
    On Mon, 21 Nov 2022 00:31:25 -0800 (PST), Daud Deden
    <daud.deden@gmail.com> wrote:

    So far, you have offered up a 'parts list' of human bipedalism features, in response to my request for "a standard meaning of bipedalism". A list of features does not a meaning make, in my experience. In all of my conversations with others about Biology
    *or* Engineering, I have never heard of a list of parts being referred to as a "standard meaning of" anything. A "standard measure" perhaps, but not a standard meaning.
    Perhaps Erika will inform what the 'standard meaning of bipedalism' is, since you rely on her authority, in addition to the parts list. But I can't see how to improve the simple statement given, "two limbs in compression", when applied to whichever the
    animate taxon under discussion.


    What is in dispute here is not the meaning of bipedalism, but instead
    what is the topic under discussion. I am interested in discussing the
    origin of human bipedalism. Are you?

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From jillery@21:1/5 to All on Tue Nov 22 01:20:01 2022
    On Mon, 21 Nov 2022 06:44:37 -0500, jillery <69jpil69@gmail.com>
    wrote:

    On Mon, 21 Nov 2022 00:31:25 -0800 (PST), Daud Deden
    <daud.deden@gmail.com> wrote:

    So far, you have offered up a 'parts list' of human bipedalism features, in response to my request for "a standard meaning of bipedalism". A list of features does not a meaning make, in my experience. In all of my conversations with others about
    Biology *or* Engineering, I have never heard of a list of parts being referred to as a "standard meaning of" anything. A "standard measure" perhaps, but not a standard meaning.
    Perhaps Erika will inform what the 'standard meaning of bipedalism' is, since you rely on her authority, in addition to the parts list. But I can't see how to improve the simple statement given, "two limbs in compression", when applied to whichever the
    animate taxon under discussion.


    What is in dispute here is not the meaning of bipedalism, but instead
    what is the topic under discussion. I am interested in discussing the
    origin of human bipedalism. Are you?


    Apparently you were but are no longer. I acknowledge your comments
    were interesting when you were.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Tue Nov 22 00:58:46 2022
    On Monday, November 21, 2022 at 6:44:39 AM UTC-5, 69jp...@gmail.com wrote:
    On Mon, 21 Nov 2022 00:31:25 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    So far, you have offered up a 'parts list' of human bipedalism features, in response to my request for "a standard meaning of bipedalism". A list of features does not a meaning make, in my experience. In all of my conversations with others about
    Biology *or* Engineering, I have never heard of a list of parts being referred to as a "standard meaning of" anything. A "standard measure" perhaps, but not a standard meaning.
    Perhaps Erika will inform what the 'standard meaning of bipedalism' is, since you rely on her authority, in addition to the parts list. But I can't see how to improve the simple statement given, "two limbs in compression", when applied to whichever
    the animate taxon under discussion.
    What is in dispute here is not the meaning of bipedalism, but instead
    what is the topic under discussion. I am interested in discussing the
    origin of human bipedalism. Are you?
    I simply clarified my position, as you did yours and Erika's. I don't view that as dispute. Different strokes/steps/opinions for different folks. IMO human bipedalism preceded humans (Homo of Chr. 2 split), and it has continued to evolve, step by step.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to 69jp...@gmail.com on Tue Nov 22 01:02:08 2022
    On Tuesday, November 22, 2022 at 1:20:03 AM UTC-5, 69jp...@gmail.com wrote:
    On Mon, 21 Nov 2022 06:44:37 -0500, jillery <69jp...@gmail.com>
    wrote:
    On Mon, 21 Nov 2022 00:31:25 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    So far, you have offered up a 'parts list' of human bipedalism features, in response to my request for "a standard meaning of bipedalism". A list of features does not a meaning make, in my experience. In all of my conversations with others about
    Biology *or* Engineering, I have never heard of a list of parts being referred to as a "standard meaning of" anything. A "standard measure" perhaps, but not a standard meaning.
    Perhaps Erika will inform what the 'standard meaning of bipedalism' is, since you rely on her authority, in addition to the parts list. But I can't see how to improve the simple statement given, "two limbs in compression", when applied to whichever
    the animate taxon under discussion.


    What is in dispute here is not the meaning of bipedalism, but instead
    what is the topic under discussion. I am interested in discussing the >origin of human bipedalism. Are you?
    Apparently you were but are no longer. I acknowledge your comments
    were interesting when you were.

    Yes, for decades past and decades into the future, discontinuously. There are other things that pop up that require attention.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to Daud Deden on Tue Nov 22 04:31:49 2022
    On Tuesday, November 22, 2022 at 4:02:10 AM UTC-5, Daud Deden wrote:
    On Tuesday, November 22, 2022 at 1:20:03 AM UTC-5, 69jp...@gmail.com wrote:
    On Mon, 21 Nov 2022 06:44:37 -0500, jillery <69jp...@gmail.com>
    wrote:
    On Mon, 21 Nov 2022 00:31:25 -0800 (PST), Daud Deden ><daud....@gmail.com> wrote:

    So far, you have offered up a 'parts list' of human bipedalism features, in response to my request for "a standard meaning of bipedalism". A list of features does not a meaning make, in my experience. In all of my conversations with others about
    Biology *or* Engineering, I have never heard of a list of parts being referred to as a "standard meaning of" anything. A "standard measure" perhaps, but not a standard meaning.
    Perhaps Erika will inform what the 'standard meaning of bipedalism' is, since you rely on her authority, in addition to the parts list. But I can't see how to improve the simple statement given, "two limbs in compression", when applied to whichever
    the animate taxon under discussion.


    What is in dispute here is not the meaning of bipedalism, but instead >what is the topic under discussion. I am interested in discussing the >origin of human bipedalism. Are you?
    Apparently you were but are no longer. I acknowledge your comments
    were interesting when you were.
    Yes, for decades past and decades into the future, discontinuously. There are other things that pop up that require attention.
    -

    Of all known hominoids & hominins, only Homo sapiens and Hylobatids have habitual upright bipedalism and a propensity to develop chins. Kow Swamp fossils are Homo sapien, their large teeth are claimed to be the reason for their chins being smaller than
    Europeans of that age. I expect that if mandibles of European Miocene apes are found, a slight chin protuberance will be seen.

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to Daud Deden on Tue Nov 22 08:37:59 2022
    On Sunday, November 20, 2022 at 11:26:11 PM UTC-5, Daud Deden wrote:
    On Sunday, November 20, 2022 at 4:50:27 AM UTC-5, Daud Deden wrote:
    On Sunday, November 20, 2022 at 2:01:18 AM UTC-5, 69jp...@gmail.com wrote:
    On Sat, 19 Nov 2022 12:43:27 -0800 (PST), Daud Deden <daud....@gmail.com> wrote:

    On Saturday, November 19, 2022 at 2:20:20 PM UTC-5, 69jp...@gmail.com wrote:
    On Sat, 19 Nov 2022 06:06:22 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Saturday, November 19, 2022 at 6:40:01 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 18 Nov 2022 03:45:32 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, November 18, 2022 at 2:12:32 AM UTC-5, 69jp...@gmail.com wrote:
    On Thu, 17 Nov 2022 15:53:51 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 12:57:57 PM UTC-5, 69jp...@gmail.com wrote:
    On Wed, 16 Nov 2022 22:42:03 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 1:29:04 AM UTC-5, Daud Deden wrote:
    On Wednesday, November 16, 2022 at 11:08:11 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 04 Nov 2022 02:21:55 -0400, jillery <69jp...@gmail.com>
    wrote:

    On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden >> >> >> >> >> > >>> <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE> >> >> >> >> >> > >>> >> >>
    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps> >> >> >> >> >> > >>> >> >>
    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a
    Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.


    My impression is there isn't enough evidence to show whether Pliocene
    African apes descended from Miocene European apes or Miocene African
    apes. Either way, there was enough time between the two eras to have
    evolved differences between either Miocene populations and Pliocene S.
    tchadensis.

    I have recently become aware of:

    <https://en.wikipedia.org/wiki/Danuvius_guggenmosi>

    which was a Miocene European ape that may have evolved arboreal
    bipedalism similar to S.tchadensis.

    Depending on how widespread its range, and how successful its
    descendants, it's plausible they lived south of the Black Sea during
    the late Miocene.

    The question then becomes whether it's more likely these apes found
    their way into Africa to become the ancestors of Pliocene
    S.tchadensis, or whether S.tchadensis evolved from Miocene African
    apes.

    Unfortunately, the habitat of these apes made their fossil
    preservation extremely rare, and so the evidence to well support
    either hypothesis is lacking.

    However, the question at least conditionally can be answered by
    comparing the likelihood of a migratory pathway during that time,
    versus the likelihood of arboreal bipedalism evolving independently in
    two populations.

    There are a number of anatomic features associated with arboreal
    bipedalism, some of which are necessary, ex. anterior foramen magnum,

    The foramen magnum is always situated relatively more anteriorly in immature than in mature apes.[ - and men. ]
    Not sure what you mean by "mature"; the individual or the species?

    Individually.
    My understanding is the relative position of foramen magnum doesn't
    change significantly during human development.

    Right. In chimps the muzzle gradually moves anteriorly relative to the foramen magnum, in Homo only the nose does.
    Sorry, I erred above, I'd meant "...than in mature apes." The "and men" was NOT meant, I thought I'd erased it! Oops.
    The positions of the muzzle and/or nose relative to the foramen magnum
    don't inform bipedalism.

    It does, in tail-less upright orthogonal striding terrestrial former/partial arboreal bipeds, it does not in hopping bipeds.
    Cf short-faced giant kangaroo (short tail, striding upright bipedal) >> The topic isn't general bipedalism, but hominoid bipedalism.
    Non-hominoid species don't inform this discussion.
    <inserted your reply in your later post>

    Topic: 'Human bipedalism'


    Fair point. To be precise, the topic is the *origin* of human bipedalism. But human bipedalism didn't originate in humans, but is derived from *hominoid* ancestors like australopiths or earlier.
    A version of hominoid bipedalism eg. Homo, hylobatid
    A version of primate bipedalism eg. Sifaka
    A version of mammal bipedalism eg. Kangaroo
    A version of animal bipedalism eg. Hoatzin (adult)
    A version of animal bipedalism eg. T.rex

    If you want to expand the discussion beyond the origins of human bipedalism, then don't limit yourself to bipedalism; include all
    animal locomotion, up to and including invertebrates. Good luck with that.
    If you want to make coherent and relevant points about the origin of human bipedalism, then constrain your comments to Homo species and
    their likely ancestors.
    That is a good way to lose useful information relative to the topic, IMO. You've just erased hylobatids from the conversation. Just like Lieberman did in his endurance running H. erectus fantasy.

    Adult chimps have protruding muzzles and are mostly qpal on the ground. Adult humans have flat faces and are bipedal on the ground.
    Either way, the important point is the position and angle of foramen
    magnum are diagnostic among all vertebrates for how they habitually
    hold their head, and so includes/excludes bipedalism among hominids.

    Yes, but no. Great apes are bipedal except when (hurrying) on open ground they adopt quadrupedalism. Homo retains the primitive bipedal gait of hominoid ancestors, as do hylobatids.
    All Homo species are great apes by definition, including H.sapiens.

    Yes, I meant 'arboreal great apes'. Humans are terrestrial great apes, hylobatids are arboreal lesser apes.

    They do/did quadrupedalism only in exceptional cases.

    https://youtu.be/pCrH6BOwxe4 15mph qpal running as a patas monkey, not a chimp.
    Imagine how much faster that person would be if he ran normally, like
    this:

    <https://www.youtube.com/watch?v=k3PZgbQ8auE>
    How is that an exceptional case among hominins? Only Usain Bolt can outrun qpal chimp at top speed.
    Your cited video shows an exceptional case among humans, which have >> relatively short arms and long legs, anatomically maladapted for
    quadrupedal locomotion.

    Humans are faster qpal palm-down sprinter and qpal endurance runner than any other hominoid.
    Patas monkey's arms are shorter than their legs: https://www.britannica.com/animal/patas-monkey

    Locomotor Anatomy and Behavior of Patas Monkeys (Erythrocebus patas) with Comparison to Vervet Monkeys (Cercopithecus aethiops)
    Adrienne L. Zihlman and Carol E. Underwood

    Additional article information

    Abstract
    Patas monkeys (Erythrocebus patas) living in African savanna woodlands and grassland habitats have a locomotor system that allows them to run fast, presumably to avoid predators. Long fore- and hindlimbs, long foot bones, short toes, and a
    digitigrade foot posture were proposed as anatomical correlates with speed. In addition to skeletal proportions, soft tissue and whole body proportions are important components of the locomotor system. To further distinguish patas anatomy from other Old
    World monkeys, a comparative study based on dissection of skin, muscle, and bone from complete individuals of patas and vervet monkeys (Cercopithecus aethiops) was undertaken. Analysis reveals that small adjustments in patas skeletal proportions,
    relative mass of limbs and tail, and specific muscle groups promote efficient sagittal limb motion. The ability to run fast is based on a locomotor system adapted for long distance walking. The patas' larger home range and longer daily range than those
    of
    vervets give them access to highly dispersed, nutritious foods, water, and sleeping trees. Furthermore, patas monkeys have physiological adaptations that enable them to tolerate and dissipate heat. These features all contribute to the distinct
    adaptation that is the patas monkeys' basis for survival in grassland and savanna woodland areas.
    Footraces between humans and patas monkeys are exceptional events.
    Also, even though his head is in extreme
    elevation, he can barely see where he's going, as his foramen magnum >> is anatomically maladapted for quadrupedal motion. Silly Guinness
    records notwithstanding, any human moving quadrupedally from a
    predator would soon become predator poop.

    Why? Carrying a blade pirate-style teeth-clenched, with a few pards similarly equipped, would present predators with a serious challenge. Bipedally, better weapons could be carried, of course, but running itself isn't enough. Patas, vervet &
    baboons climb trees, qpal running is just the short sprint to flight.
    Imagine yourself running quadrupedally with a blade pirate-style teeth clenched. Now imagine yourself running out of breath and exhausted as the predator you're running from catches up and eats you.
    Don't bring a fang to a knife fight. Don't run with scissors. But most importantly, don't get encircled, because then you're prey. My pards and I run out only far enough to encircle said predator, then sing kumbaya as we slash it into ribbons of
    jerky. Predators attack from behind. There is no behind in a circle. But there is a vulnerable behind in an encircled predator. That is why the first knife slashes a rear hamstring/achilles/artery, while a pard is taunting up front, keeping the predator'
    s attention away. Being quadrupedal with a knife is less useful than being bipedal with a knife. But it by no means is as vulnerable as being bipedal without one.
    Fun is fun, but at least make your jokes relevant to the topic.
    and some of which are incidental, ex. molar patterns. Descendant
    populations are more likely to share these features than are
    independent populations. This suggests to me that a sufficiently
    robust fossil record could answer this question with some degree of
    certainty.

    Alternately, my understanding is southern Europe and central Africa
    are ecological opposites, in the sense that when one is hot and dry
    the other is temperate and wet.
    Central Africa is and was hot,
    ... and wet aka tropical,

    The adoption of qpal knucklewalking by African apes indicates that their ancient habitat went through a dry phase (rainforest became patchy) forcing a terrestrial dog-like gait.
    Perhaps. My understanding is bipedal arboreal apes continued to walk
    bipedally on the ground, while non-bipedal arboreal apes also adopted
    quadrupedal habits on the ground.

    Bipedal walking is primitive in arboreal hominoids, quadrupedal walking is derived. I don't know of any 'non-bipedal arboreal apes', only monkeys.
    That's not my understanding. My understanding is chimpanzees,
    gorillas, and orangutans are non-bipedal arboreal apes, meaning when
    they are in the trees, they do not walk upright.

    Their body orientation on and under branches is primarily upright, not pronograde with all limbs in compression aka quadrupedal. The modern AMHs orthogonal posture is derived, not the same as primitive upright bipedal arboreal hominoids.
    You continue to use above a non-standard meaning of bipedalism.

    Please direct me to "a standard meaning of bipedalism". Afaik, bipedalism is a trait of locomoting on 2 legs in compression, whether the hands are swinging, carrying or plucking.
    Sloths are quadrumanual, orangs are also called that when hanging tensionally from four limbs, but bipedal when walking on thick branches.
    I acknowledge I am no authority to assert a standard meaning of
    *human* bipedalism. But I rely on the list of diagnostic features as described by Erika's aka Gutsick Gibbon's, who is at least one authority. From the video you cited previously:

    <https://youtu.be/jo2ZLnucuHY>

    1. Foramen magnum and occipital condyles positioned anterior and
    angled vertically.

    2. Vertebrate lumbar lordosis.

    3. Bowl-shaped pelvis with sagittally oriented iliia and anterior
    iliac spine.

    4. Broad sacrum.

    5. Thick cortical bone around femur neck.

    6. Flattened elliptical distal condyles.

    7. Opterator externus groove.

    8. Valgus knee.

    9. Three arches of foot's sole.

    Also, I note that Erika expressed the same criticism I did about your quadrupedal human, that the foramen magnum precludes such habitual behavior.
    Rather obvious that. Yet we can do it, quickly when we have to. Our body form is closer to monkeys than to apes in some ways.

    A list of features does not a meaning make.

    Please direct me to "a standard meaning of bipedalism". You demanded it, I requested it.
    Because there are some octopi that notoriously walk bipedally, they don't have any of those features.
    BUT THEY DO WALK ON TWO LIMBS IN COMPRESSION. And **THAT** is the standard meaning of bipedalism.
    So you must incorporate that into your description of human bipedalism. And so should Erika.
    Hanging from branches using combinations of limbs isn't bipedalism any
    more than is climbing up coconut palms.

    Suspension itself is not bipedalism.
    That's what I said.
    As were most
    arboreal apes prior to Australopithecines.
    just right for the evolution of small bipedal arboreal apes. >> >> >> >
    The fact that there are no small bipedal arboreal apes in Africa indicates that there was some climate shifting.
    Again perhaps. It also suggests small bipedal arboreal apes were
    outcompeted.

    They were, by monkeys which were more ground adapted, able to swiftly run between forest stands during a drier climate phase.

    the southern Black Sea is between temperate and tropical. >> >> >> >> Correct. Southern Europe and the Black Sea are at the same latitudes.
    This suggests they would tend to have the same climate. However, the
    Black Sea is farther inland, and so suffers more continental extremes.
    So any climate changes will appear first around the Black Sea and
    become more extreme compared to southern Europe.

    I'm talking about from 11ma through the MSC to 5ma. The Medit. & Red Seas dried out, the Black Sea didn't.
    The relative position of the Black Sea didn't change from then to now.
    The important point is its position is deep in Eurasia, where >> >> >> continental climates rule.

    It lies between the Atlantic-Mediterranean and the Caspian Sea, in the Peri-Tethyan basin, protected by the high Iranian plateau to the south. Not a typical continental climate.
    <https://www.britannica.com/place/Black-Sea/Climate>
    **********************************
    The climate of the landlocked Black Sea can be characterized generally
    as continental (i.e., subject to pronounced seasonal temperature >> >> variations), although climatic conditions in some parts of the basin
    are controlled to a great extent by the shoreline relief. A steppe >> >> climate, with cold winters and hot, dry summers, is found in the >> >> northwestern part of the basin exposed to the influence of air masses
    from the north.
    ************************************

    Summer in north including Bavaria via Danube valley, winter in south including visits further southwardly.
    I suppose Miocene apes collected frequent-flier miles.
    They weren't sessile, but very mobile.
    I am unaware of any arboreal species which seasonally migrate.
    Songbirds? If you meant hominoids only, they are all tropical. Miocene apes had warm/cool seasons, they did migrate.
    To the
    best of my knowledge, although they may have a large home range, they stick to one area throughout the year. This would suggest migrating Miocene arboreal apes are a unique exception. Do you know of any
    extant arboreal animals which seasonally migrate?
    Songbirds? Which 'arboreal animals' do you mean, hominoids only?
    My understanding is the Mediterranean dried out only about 6mya, long
    after European, and presumably Black Sea, arboreal apes went extinct.

    No, Danuvius and later Miocene apes there were of one lineage IMO, that may have lived there until 5ma, with successive expansional waves emigrating outwardly including towards Africa.

    The Red Sea is too far south to affect migration from Europe to Africa
    regardless of climate patterns.

    It is part of the African-Anatolian rift.
    I acknowledge that rift was one plausible pathway from Europe to >> >> Africa. The Red Sea was not, nor did it block such a pathway.

    I include it provisionally, more data needed.
    Sounds like a segue for aquatic ape hypothesis.

    Most proponents of that hypothesis tend to refuse to acknowledge that all extant (and by extension, archaic) Homo sleep well sheltered (dry, warm, shielded) from the elements (or try to be). Thus it is unrealistic imo.
    Of course, I refer to the surrounding region, which today is hyper-arid


    Moving toward 30 degrees latitude, rainfall becomes seasonally dry,
    and then almost continuously dry. My understanding is, the only
    native forests south of the Caspian are in the mountains, and adjacent
    to the Mediterranean coasts. Arboreal apes of any kind would find
    these deserts impassible.

    You are speaking of recent climate. There are no arboreal apes there now.
    No, I am speaking of climate then *and* now. Regions around 30 >> >> >> degrees latitude tend to be drier than those around the equator, with
    exceptions due to terrain and ocean currents.
    Another stop.
    Stop temporarily.
    Ok, stop as in "be right back". But this isn't a real-time chat.
    What's the point of mentioning it?
    To inform that I was stopping until i could get wifi again.
    Unclear. Do you mean stop migration temporarily? If so, keep in mind >> that the same climate changes which would create arid conditions
    around 30 degrees latitude would also shrink forests further north and
    south.
    You appear to be claiming that the European Miocene apes could never have been linked to African and Asian apes. Yet they certainly were, else they wouldn't have existed at all.
    Such an "appearance" is incorrect. In certain cases, regions around
    30 degrees latitude have/had enough rainfall to support forests. The
    relevant point here is, global climate since the Miocene has gotten
    colder and drier, especially around 30 degrees latitude, which has led
    to the creation of large areas of treeless savannah and desert. I >> >> don't know when European and African forests separated. Do you?

    Also, the question isn't about the origin of apes generally. It's >> >> about the origin of arboreal bipedal apes. We know they existed in >> >> Pliocene Africa. They *may* have existed in Miocene Europe. Even if
    they did, the two populations may still have evolved independently.
    To a first approximation, average rainfall and temperature are
    functions of latitude. However, while temperature is a function of
    the sine of latitude, rainfall is more complex. It tends to be
    continuously heavy near the equator, continuously dry near 30 degrees,
    and seasonally variable between 30 and 60 degrees. This general
    pattern is modified, sometimes dramatically, by terrain, ocean
    currents, seasons, and Milankovitch cycles.

    The most significant variable is Africa's northward tectonic >> >> >> >> migration, about a centimeter a year since before the Miocene. So,
    while central Africa has moved from south to north of the equator with
    little effect, north Africa has approached and then went north of 30
    degrees, making it over time ever drier, amplifying other climate
    trends, making once wooded areas into vast savannah and desert.

    Yes.

    Also, Africa's tectonic slide north almost certainly pinched closed
    the Gilbraltar Sttraits, which caused the Mediterranean to dry up at
    least once, and likely several times as sea levels rose and fell. The
    resulting hot salt basin would also have been impassible for arboreal
    apes.
    This is as true now as it was in the
    Miocene. This suggests to me there could not have been an unbroken
    forested path for arboreal apes to migrate between Europe/Near East
    and Central Africa.
    I would not claim nor disclaim that. The Levant is near the midpoint, extends the African Rift valley to Anatolia, is a major avian migration route between Africa and Eurasia, has fossil/artifacts of Homo erectus, neanderthal &
    sapiens oldest known cooking (fish .78ma) and earliest waternut gathering and bread making. The region is amenable to hominins & Homo.
    I acknowledge the facts you describe above. However, the Levant is
    savannah and desert except for a narrow strip along the Mediterranean
    and up in the mountains. While this is no problem for terrestrial
    bipeds like Homo, ISTM arboreal hominids like D.guggenmosi would have
    a much harder time living/migrating there.

    "is".
    Again, refer to microclimate of Levant 11ma - 5ma. Today's Dead Sea was once the vast brackish Lake Lisan that reached to Lebanon, a gallery forest may have reached from Anatolia to Egypt.
    The regions you describe above are part of the Mediterranean coastal
    mountains I mentioned previously.

    The Dead Sea is by no means a coastal mountain region.
    https://en.wikipedia.org/wiki/Judaean_Mountains

    These are part of a series of ranges all along the eastern
    Mediterranean coast.
    I agree a coastal Mediterranean
    forest is plausible.

    I'm referring to the tectonic rift valley between Zimbabwe/Zambia and Lebanon/Anatolia.
    ... which runs parallel to the Mediterranean coast.
    Of course, there were coastal forests as well, but they were affected by the MSC.

    However, my understanding is the evidence is
    insufficient to say if it would have been as extensive and continuous
    as you suggest during the time you suggest.

    Haven't got enough hard data yet.
    Cite the data you think is sufficient to answer this question.
    What is ISTM?


    It's shorthand acronym for "It Seems To Me"

    Ok, thanks.

    Danuvius, Rudapithecus, Graecopithecus, Oranopithecus each had a unique trait shared with hominins. I think of them as a superspecies with local variations.
    -
    If you place Danuvius half-way between fast brachiating bipedal long backed long achilles tendon hylobatids and bipedal Homo with long back and long achilles tendon, it fits perfectly.

    Wiki:
    Danuvius is thought to have had a broad chest. It is the first recorded Miocene great ape to have had the diaphragm located in the lower chest cavity, as in Homo, indicating an extended lower back and a greater number of functional
    lumbar vertebrae. This may have caused lordosis (the normal curvature of the human spine) and moved the center of mass over the hips and legs, which implies some habitual bipedal activity.

    The robust finger and hypertrophied wrist and elbow bones indicate a strong grip and load bearing adaptations for the arms. The legs also show adaptations for load-bearing, especially at the hypertrophied knee joint. There was likely
    limited ankle loading, and the ankle would have had a hinge-like function, being most stable if positioned perpendicularly to the leg as opposed to at an angle in apes. Danuvius was likely able to achieve a strong grip with its big toes, unlike modern
    African great apes, which would have allowed it to grasp onto thinner trees. The limb proportions are most similar to those of bonobos.
    ---
    Q: Alex, what is Sifaka?
    -

    The Origins of Bipedal Locomotion
    William EH Harcourt-Smith 2013
    Handbook of PA doi 10.1007/978-3-642-27800-6_48-3

    Abstract

    [continued in next message]

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Daud Deden@21:1/5 to Daud Deden on Sun Nov 27 16:36:46 2022
    On Tuesday, November 22, 2022 at 11:38:01 AM UTC-5, Daud Deden wrote:
    On Sunday, November 20, 2022 at 11:26:11 PM UTC-5, Daud Deden wrote:
    On Sunday, November 20, 2022 at 4:50:27 AM UTC-5, Daud Deden wrote:
    On Sunday, November 20, 2022 at 2:01:18 AM UTC-5, 69jp...@gmail.com wrote:
    On Sat, 19 Nov 2022 12:43:27 -0800 (PST), Daud Deden <daud....@gmail.com> wrote:

    On Saturday, November 19, 2022 at 2:20:20 PM UTC-5, 69jp...@gmail.com wrote:
    On Sat, 19 Nov 2022 06:06:22 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Saturday, November 19, 2022 at 6:40:01 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 18 Nov 2022 03:45:32 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Friday, November 18, 2022 at 2:12:32 AM UTC-5, 69jp...@gmail.com wrote:
    On Thu, 17 Nov 2022 15:53:51 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 12:57:57 PM UTC-5, 69jp...@gmail.com wrote:
    On Wed, 16 Nov 2022 22:42:03 -0800 (PST), Daud Deden
    <daud....@gmail.com> wrote:

    On Thursday, November 17, 2022 at 1:29:04 AM UTC-5, Daud Deden wrote:
    On Wednesday, November 16, 2022 at 11:08:11 AM UTC-5, 69jp...@gmail.com wrote:
    On Fri, 04 Nov 2022 02:21:55 -0400, jillery <69jp...@gmail.com>
    wrote:

    On Thu, 3 Nov 2022 20:32:40 -0700 (PDT), Daud Deden >> >> >> >> >> > ><daud....@gmail.com> wrote:

    On Thursday, November 3, 2022 at 6:29:01 PM UTC-4, 69jp...@gmail.com wrote:
    On Thu, 3 Nov 2022 07:56:05 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Tuesday, November 1, 2022 at 4:17:31 AM UTC-4, 69jp...@gmail.com wrote:
    On Mon, 31 Oct 2022 15:15:01 -0700 (PDT), Daud Deden
    <daud....@gmail.com> wrote:

    On Monday, October 24, 2022 at 2:50:22 AM UTC-4, 69jp...@gmail.com wrote:
    Gutsick Gibbon is the Youtube handle of a biological anthropology PhD
    student named Eriks. Two of her recent videos discuss some of the
    latest developments relating to the origins of human bipedalism:

    <https://www.youtube.com/watch?v=kbQAgPSHbZE>

    The above is a link to a 32-minute video where Erika discusses several
    papers relating to Sahelanthropus tchadensis. This fossil is
    remarkable in part because it's dated to about 7mya and was found in
    central-african Chad, and also because it may be the oldest bipedal
    hominin fossil found to date. However, there appears to be strong
    disagreement whether the evidence supports bipedalism.

    <https://www.youtube.com/watch?v=Nwkfkp360ps>

    The above is a link to a 22-minute video where Erika discusses several
    hypotheses about *why* our ancestors shifted to obligate bipedalism.
    She discusses several hypotheses, and presents compelling arguments
    for her preferred one.
    -
    Video by Erika on Lucy bipedalism: https://youtu.be/jo2ZLnucuHY
    Thank you for citing the above video. It's prelude to the ones I
    cited, and refers to them, and so complete a logical trilogy.

    In another video, she says that Sahelanthropus was the LCA of Homo / Pan, (though probably just in the general sense). https://www.youtube.com/watch?v=g4FTbZLkpzU&t=7s
    In my view, Sahelanthropus is just a southwestern European Miocene ape *Descendant*, very similar to their eastern and northern kin. I see nothing palmigrade in any Miocene ape.
    Sahelanthropus tchadensis is neither Miocene nor European, but is a
    Pliocene central African species.
    Yes, I claim it is *descended from* European Miocene apes of the Black Sea region.


    My impression is there isn't enough evidence to show whether Pliocene
    African apes descended from Miocene European apes or Miocene African
    apes. Either way, there was enough time between the two eras to have
    evolved differences between either Miocene populations and Pliocene S.
    tchadensis.

    I have recently become aware of:

    <https://en.wikipedia.org/wiki/Danuvius_guggenmosi> >> >> >> >> >> >
    which was a Miocene European ape that may have evolved arboreal
    bipedalism similar to S.tchadensis.

    Depending on how widespread its range, and how successful its
    descendants, it's plausible they lived south of the Black Sea during
    the late Miocene.

    The question then becomes whether it's more likely these apes found
    their way into Africa to become the ancestors of Pliocene
    S.tchadensis, or whether S.tchadensis evolved from Miocene African
    apes.

    Unfortunately, the habitat of these apes made their fossil
    preservation extremely rare, and so the evidence to well support
    either hypothesis is lacking.

    However, the question at least conditionally can be answered by
    comparing the likelihood of a migratory pathway during that time,
    versus the likelihood of arboreal bipedalism evolving independently in
    two populations.

    There are a number of anatomic features associated with arboreal
    bipedalism, some of which are necessary, ex. anterior foramen magnum,

    The foramen magnum is always situated relatively more anteriorly in immature than in mature apes.[ - and men. ]
    Not sure what you mean by "mature"; the individual or the species?

    Individually.
    My understanding is the relative position of foramen magnum doesn't
    change significantly during human development.

    Right. In chimps the muzzle gradually moves anteriorly relative to the foramen magnum, in Homo only the nose does.
    Sorry, I erred above, I'd meant "...than in mature apes." The "and men" was NOT meant, I thought I'd erased it! Oops.
    The positions of the muzzle and/or nose relative to the foramen magnum
    don't inform bipedalism.

    It does, in tail-less upright orthogonal striding terrestrial former/partial arboreal bipeds, it does not in hopping bipeds.
    Cf short-faced giant kangaroo (short tail, striding upright bipedal)
    The topic isn't general bipedalism, but hominoid bipedalism.
    Non-hominoid species don't inform this discussion.
    <inserted your reply in your later post>

    Topic: 'Human bipedalism'


    Fair point. To be precise, the topic is the *origin* of human bipedalism. But human bipedalism didn't originate in humans, but is derived from *hominoid* ancestors like australopiths or earlier.
    A version of hominoid bipedalism eg. Homo, hylobatid
    A version of primate bipedalism eg. Sifaka
    A version of mammal bipedalism eg. Kangaroo
    A version of animal bipedalism eg. Hoatzin (adult)
    A version of animal bipedalism eg. T.rex

    If you want to expand the discussion beyond the origins of human bipedalism, then don't limit yourself to bipedalism; include all animal locomotion, up to and including invertebrates. Good luck with that.
    If you want to make coherent and relevant points about the origin of human bipedalism, then constrain your comments to Homo species and their likely ancestors.
    That is a good way to lose useful information relative to the topic, IMO. You've just erased hylobatids from the conversation. Just like Lieberman did in his endurance running H. erectus fantasy.

    Adult chimps have protruding muzzles and are mostly qpal on the ground. Adult humans have flat faces and are bipedal on the ground.
    Either way, the important point is the position and angle of foramen
    magnum are diagnostic among all vertebrates for how they habitually
    hold their head, and so includes/excludes bipedalism among hominids.

    Yes, but no. Great apes are bipedal except when (hurrying) on open ground they adopt quadrupedalism. Homo retains the primitive bipedal gait of hominoid ancestors, as do hylobatids.
    All Homo species are great apes by definition, including H.sapiens.

    Yes, I meant 'arboreal great apes'. Humans are terrestrial great apes, hylobatids are arboreal lesser apes.

    They do/did quadrupedalism only in exceptional cases.

    https://youtu.be/pCrH6BOwxe4 15mph qpal running as a patas monkey, not a chimp.
    Imagine how much faster that person would be if he ran normally, like
    this:

    <https://www.youtube.com/watch?v=k3PZgbQ8auE>
    How is that an exceptional case among hominins? Only Usain Bolt can outrun qpal chimp at top speed.
    Your cited video shows an exceptional case among humans, which have >> relatively short arms and long legs, anatomically maladapted for
    quadrupedal locomotion.

    Humans are faster qpal palm-down sprinter and qpal endurance runner than any other hominoid.
    Patas monkey's arms are shorter than their legs: https://www.britannica.com/animal/patas-monkey

    Locomotor Anatomy and Behavior of Patas Monkeys (Erythrocebus patas) with Comparison to Vervet Monkeys (Cercopithecus aethiops)
    Adrienne L. Zihlman and Carol E. Underwood

    Additional article information

    Abstract
    Patas monkeys (Erythrocebus patas) living in African savanna woodlands and grassland habitats have a locomotor system that allows them to run fast, presumably to avoid predators. Long fore- and hindlimbs, long foot bones, short toes, and a
    digitigrade foot posture were proposed as anatomical correlates with speed. In addition to skeletal proportions, soft tissue and whole body proportions are important components of the locomotor system. To further distinguish patas anatomy from other Old
    World monkeys, a comparative study based on dissection of skin, muscle, and bone from complete individuals of patas and vervet monkeys (Cercopithecus aethiops) was undertaken. Analysis reveals that small adjustments in patas skeletal proportions,
    relative mass of limbs and tail, and specific muscle groups promote efficient sagittal limb motion. The ability to run fast is based on a locomotor system adapted for long distance walking. The patas' larger home range and longer daily range than those
    of
    vervets give them access to highly dispersed, nutritious foods, water, and sleeping trees. Furthermore, patas monkeys have physiological adaptations that enable them to tolerate and dissipate heat. These features all contribute to the distinct
    adaptation that is the patas monkeys' basis for survival in grassland and savanna woodland areas.
    Footraces between humans and patas monkeys are exceptional events.
    Also, even though his head is in extreme
    elevation, he can barely see where he's going, as his foramen magnum
    is anatomically maladapted for quadrupedal motion. Silly Guinness >> records notwithstanding, any human moving quadrupedally from a
    predator would soon become predator poop.

    Why? Carrying a blade pirate-style teeth-clenched, with a few pards similarly equipped, would present predators with a serious challenge. Bipedally, better weapons could be carried, of course, but running itself isn't enough. Patas, vervet &
    baboons climb trees, qpal running is just the short sprint to flight.
    Imagine yourself running quadrupedally with a blade pirate-style teeth clenched. Now imagine yourself running out of breath and exhausted as the predator you're running from catches up and eats you.
    Don't bring a fang to a knife fight. Don't run with scissors. But most importantly, don't get encircled, because then you're prey. My pards and I run out only far enough to encircle said predator, then sing kumbaya as we slash it into ribbons of
    jerky. Predators attack from behind. There is no behind in a circle. But there is a vulnerable behind in an encircled predator. That is why the first knife slashes a rear hamstring/achilles/artery, while a pard is taunting up front, keeping the predator'
    s attention away. Being quadrupedal with a knife is less useful than being bipedal with a knife. But it by no means is as vulnerable as being bipedal without one.
    Fun is fun, but at least make your jokes relevant to the topic.
    and some of which are incidental, ex. molar patterns. Descendant
    populations are more likely to share these features than are
    independent populations. This suggests to me that a sufficiently
    robust fossil record could answer this question with some degree of
    certainty.

    Alternately, my understanding is southern Europe and central Africa
    are ecological opposites, in the sense that when one is hot and dry
    the other is temperate and wet.
    Central Africa is and was hot,
    ... and wet aka tropical,

    The adoption of qpal knucklewalking by African apes indicates that their ancient habitat went through a dry phase (rainforest became patchy) forcing a terrestrial dog-like gait.
    Perhaps. My understanding is bipedal arboreal apes continued to walk
    bipedally on the ground, while non-bipedal arboreal apes also adopted
    quadrupedal habits on the ground.

    Bipedal walking is primitive in arboreal hominoids, quadrupedal walking is derived. I don't know of any 'non-bipedal arboreal apes', only monkeys.
    That's not my understanding. My understanding is chimpanzees,
    gorillas, and orangutans are non-bipedal arboreal apes, meaning when
    they are in the trees, they do not walk upright.

    Their body orientation on and under branches is primarily upright, not pronograde with all limbs in compression aka quadrupedal. The modern AMHs orthogonal posture is derived, not the same as primitive upright bipedal arboreal hominoids.
    You continue to use above a non-standard meaning of bipedalism.

    Please direct me to "a standard meaning of bipedalism". Afaik, bipedalism is a trait of locomoting on 2 legs in compression, whether the hands are swinging, carrying or plucking.
    Sloths are quadrumanual, orangs are also called that when hanging tensionally from four limbs, but bipedal when walking on thick branches.
    I acknowledge I am no authority to assert a standard meaning of *human* bipedalism. But I rely on the list of diagnostic features as described by Erika's aka Gutsick Gibbon's, who is at least one authority. From the video you cited previously:

    <https://youtu.be/jo2ZLnucuHY>

    1. Foramen magnum and occipital condyles positioned anterior and angled vertically.

    2. Vertebrate lumbar lordosis.

    3. Bowl-shaped pelvis with sagittally oriented iliia and anterior iliac spine.

    4. Broad sacrum.

    5. Thick cortical bone around femur neck.

    6. Flattened elliptical distal condyles.

    7. Opterator externus groove.

    8. Valgus knee.

    9. Three arches of foot's sole.

    Also, I note that Erika expressed the same criticism I did about your quadrupedal human, that the foramen magnum precludes such habitual behavior.
    Rather obvious that. Yet we can do it, quickly when we have to. Our body form is closer to monkeys than to apes in some ways.

    A list of features does not a meaning make.

    Please direct me to "a standard meaning of bipedalism". You demanded it, I requested it.
    Because there are some octopi that notoriously walk bipedally, they don't have any of those features.
    BUT THEY DO WALK ON TWO LIMBS IN COMPRESSION. And **THAT** is the standard meaning of bipedalism.
    So you must incorporate that into your description of human bipedalism. And so should Erika.
    Hanging from branches using combinations of limbs isn't bipedalism any
    more than is climbing up coconut palms.

    Suspension itself is not bipedalism.
    That's what I said.
    As were most
    arboreal apes prior to Australopithecines.
    just right for the evolution of small bipedal arboreal apes.

    The fact that there are no small bipedal arboreal apes in Africa indicates that there was some climate shifting.
    Again perhaps. It also suggests small bipedal arboreal apes were
    outcompeted.

    They were, by monkeys which were more ground adapted, able to swiftly run between forest stands during a drier climate phase.

    the southern Black Sea is between temperate and tropical.
    Correct. Southern Europe and the Black Sea are at the same latitudes.
    This suggests they would tend to have the same climate. However, the
    Black Sea is farther inland, and so suffers more continental extremes.
    So any climate changes will appear first around the Black Sea and
    become more extreme compared to southern Europe.

    I'm talking about from 11ma through the MSC to 5ma. The Medit. & Red Seas dried out, the Black Sea didn't.
    The relative position of the Black Sea didn't change from then to now.
    The important point is its position is deep in Eurasia, where >> >> >> continental climates rule.

    It lies between the Atlantic-Mediterranean and the Caspian Sea, in the Peri-Tethyan basin, protected by the high Iranian plateau to the south. Not a typical continental climate.
    <https://www.britannica.com/place/Black-Sea/Climate>
    **********************************
    The climate of the landlocked Black Sea can be characterized generally
    as continental (i.e., subject to pronounced seasonal temperature >> >> variations), although climatic conditions in some parts of the basin
    are controlled to a great extent by the shoreline relief. A steppe
    climate, with cold winters and hot, dry summers, is found in the >> >> northwestern part of the basin exposed to the influence of air masses
    from the north.
    ************************************

    Summer in north including Bavaria via Danube valley, winter in south including visits further southwardly.
    I suppose Miocene apes collected frequent-flier miles.
    They weren't sessile, but very mobile.
    I am unaware of any arboreal species which seasonally migrate.
    Songbirds? If you meant hominoids only, they are all tropical. Miocene apes had warm/cool seasons, they did migrate.
    To the
    best of my knowledge, although they may have a large home range, they stick to one area throughout the year. This would suggest migrating Miocene arboreal apes are a unique exception. Do you know of any extant arboreal animals which seasonally migrate?
    Songbirds? Which 'arboreal animals' do you mean, hominoids only?
    My understanding is the Mediterranean dried out only about 6mya, long
    after European, and presumably Black Sea, arboreal apes went extinct.

    No, Danuvius and later Miocene apes there were of one lineage IMO, that may have lived there until 5ma, with successive expansional waves emigrating outwardly including towards Africa.

    The Red Sea is too far south to affect migration from Europe to Africa
    regardless of climate patterns.

    It is part of the African-Anatolian rift.
    I acknowledge that rift was one plausible pathway from Europe to >> >> Africa. The Red Sea was not, nor did it block such a pathway.

    I include it provisionally, more data needed.
    Sounds like a segue for aquatic ape hypothesis.

    Most proponents of that hypothesis tend to refuse to acknowledge that all extant (and by extension, archaic) Homo sleep well sheltered (dry, warm, shielded) from the elements (or try to be). Thus it is unrealistic imo.
    Of course, I refer to the surrounding region, which today is hyper-arid


    Moving toward 30 degrees latitude, rainfall becomes seasonally dry,
    and then almost continuously dry. My understanding is, the only
    native forests south of the Caspian are in the mountains, and adjacent
    to the Mediterranean coasts. Arboreal apes of any kind would find
    these deserts impassible.

    You are speaking of recent climate. There are no arboreal apes there now.
    No, I am speaking of climate then *and* now. Regions around 30
    degrees latitude tend to be drier than those around the equator, with
    exceptions due to terrain and ocean currents.
    Another stop.
    Stop temporarily.
    Ok, stop as in "be right back". But this isn't a real-time chat. What's the point of mentioning it?
    To inform that I was stopping until i could get wifi again.
    Unclear. Do you mean stop migration temporarily? If so, keep in mind
    that the same climate changes which would create arid conditions
    around 30 degrees latitude would also shrink forests further north and
    south.
    You appear to be claiming that the European Miocene apes could never have been linked to African and Asian apes. Yet they certainly were, else they wouldn't have existed at all.
    Such an "appearance" is incorrect. In certain cases, regions around
    30 degrees latitude have/had enough rainfall to support forests. The
    relevant point here is, global climate since the Miocene has gotten
    colder and drier, especially around 30 degrees latitude, which has led
    to the creation of large areas of treeless savannah and desert. I
    don't know when European and African forests separated. Do you? >> >>
    Also, the question isn't about the origin of apes generally. It's
    about the origin of arboreal bipedal apes. We know they existed in
    Pliocene Africa. They *may* have existed in Miocene Europe. Even if
    they did, the two populations may still have evolved independently.
    To a first approximation, average rainfall and temperature are
    functions of latitude. However, while temperature is a function of
    the sine of latitude, rainfall is more complex. It tends to be
    continuously heavy near the equator, continuously dry near 30 degrees,
    and seasonally variable between 30 and 60 degrees. This general
    pattern is modified, sometimes dramatically, by terrain, ocean
    currents, seasons, and Milankovitch cycles.

    The most significant variable is Africa's northward tectonic
    migration, about a centimeter a year since before the Miocene. So,
    while central Africa has moved from south to north of the equator with
    little effect, north Africa has approached and then went north of 30
    degrees, making it over time ever drier, amplifying other climate
    trends, making once wooded areas into vast savannah and desert.

    Yes.

    Also, Africa's tectonic slide north almost certainly pinched closed
    the Gilbraltar Sttraits, which caused the Mediterranean to dry up at
    least once, and likely several times as sea levels rose and fell. The
    resulting hot salt basin would also have been impassible for arboreal
    apes.
    This is as true now as it was in the
    Miocene. This suggests to me there could not have been an unbroken
    forested path for arboreal apes to migrate between Europe/Near East
    and Central Africa.
    I would not claim nor disclaim that. The Levant is near the midpoint, extends the African Rift valley to Anatolia, is a major avian migration route between Africa and Eurasia, has fossil/artifacts of Homo erectus, neanderthal &
    sapiens oldest known cooking (fish .78ma) and earliest waternut gathering and bread making. The region is amenable to hominins & Homo.
    I acknowledge the facts you describe above. However, the Levant is
    savannah and desert except for a narrow strip along the Mediterranean
    and up in the mountains. While this is no problem for terrestrial
    bipeds like Homo, ISTM arboreal hominids like D.guggenmosi would have
    a much harder time living/migrating there.

    "is".
    Again, refer to microclimate of Levant 11ma - 5ma. Today's Dead Sea was once the vast brackish Lake Lisan that reached to Lebanon, a gallery forest may have reached from Anatolia to Egypt.
    The regions you describe above are part of the Mediterranean coastal
    mountains I mentioned previously.

    The Dead Sea is by no means a coastal mountain region.
    https://en.wikipedia.org/wiki/Judaean_Mountains

    These are part of a series of ranges all along the eastern
    Mediterranean coast.
    I agree a coastal Mediterranean
    forest is plausible.

    I'm referring to the tectonic rift valley between Zimbabwe/Zambia and Lebanon/Anatolia.
    ... which runs parallel to the Mediterranean coast.
    Of course, there were coastal forests as well, but they were affected by the MSC.

    However, my understanding is the evidence is
    insufficient to say if it would have been as extensive and continuous
    as you suggest during the time you suggest.

    Haven't got enough hard data yet.
    Cite the data you think is sufficient to answer this question. >> >> >> >What is ISTM?


    It's shorthand acronym for "It Seems To Me"

    Ok, thanks.

    Danuvius, Rudapithecus, Graecopithecus, Oranopithecus each had a unique trait shared with hominins. I think of them as a superspecies with local variations.
    -
    If you place Danuvius half-way between fast brachiating bipedal long backed long achilles tendon hylobatids and bipedal Homo with long back and long achilles tendon, it fits perfectly.

    Wiki:
    Danuvius is thought to have had a broad chest. It is the first recorded Miocene great ape to have had the diaphragm located in the lower chest cavity, as in Homo, indicating an extended lower back and a greater number of functional
    lumbar vertebrae. This may have caused lordosis (the normal curvature of the human spine) and moved the center of mass over the hips and legs, which implies some habitual bipedal activity.

    The robust finger and hypertrophied wrist and elbow bones indicate a strong grip and load bearing adaptations for the arms. The legs also show adaptations for load-bearing, especially at the hypertrophied knee joint. There was likely
    limited ankle loading, and the ankle would have had a hinge-like function, being most stable if positioned perpendicularly to the leg as opposed to at an angle in apes. Danuvius was likely able to achieve a strong grip with its big toes, unlike modern
    African great apes, which would have allowed it to grasp onto thinner trees. The limb proportions are most similar to those of bonobos.
    ---
    Q: Alex, what is Sifaka?
    -
    The Origins of Bipedal Locomotion
    William EH Harcourt-Smith 2013
    Handbook of PA doi 10.1007/978-3-642-27800-6_48-3
    Abstract

    [continued in next message]

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From marc verhaegen@21:1/5 to All on Fri Mar 10 13:50:59 2023
    "The Origins of Bipedal Locomotion"
    William EH Harcourt-Smith 2013 Handbook of PA doi 10.1007/978-3-642-27800-6_48-3
    BPism is a highly specialized & unusual form of primate locomotion, found today only in Hs.
    Most extinct taxa within the Hominini were BP, but to which degree?
    The significant discoveries of fossil hominin remains in the last 40 yrs have resulted in this debate becoming increasingly focused on how BP certain fossil taxa were, rather than on the overall process. Although the early hominin fossil record remains
    poor, evidence points to at least 2 distinct adaptive shifts:
    1) There was a shift to habitual BPism, as typified by certain members of Australopithecus, but possibly incl. earlier genera such as Ardipithecus & Orrorin.
    Such taxa were BP, but also retained significant adaptations to arboreal climbing.
    2) The 2nd shift was to fully obligate BPism, it coincides with the emergence of the genus Homo.
    By the Early-Pleistocene, certain members of Homo had acquired post-crania indicating fully Hs-like striding BPism.
    The final part of this chapter reviews why BPism was selected for.
    There have been many theoretical explanations,
    the most robust remain those linked to the emergence of more varied habitats. Such an environmental shift would have involved strong selection for new behavioral strategies most likely linked to the efficient procurement of food.

    ???
    Almost completely wrong.
    Miocene Hominoidea were already BP, not for running, of course, but for wading upright in the swamp forests where they fossilized, and for climbing arms overhead in the branches above the swamp,
    google "aquarboreal" (aqua=water, arbor=tree).
    Australopiths were habitually aquarboreal, and all great apes are still occasionally aquarboreal (in spite of Pleistocene coolings), wading for sedges, rice, waterlilies etc., google e.g. "bonobo wading".
    For an unbiased (comparative, non-afrocentric, non-anthropocentric) view of human evolution, google e.g. "GondwanaTalks Verhaegen".

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From marc verhaegen@21:1/5 to All on Fri Mar 17 12:31:03 2023
    Op dinsdag 22 november 2022 om 17:38:01 UTC+1 schreef Daud Deden:

    The Origins of Bipedal Locomotion
    William EH Harcourt-Smith 2013
    Handbook of PA doi 10.1007/978-3-642-27800-6_48-3
    Abstract
    Bipedalism is a highly specialized and unusual form of primate locomotion that is found today only in modern humans. [DD: Sifaka, Hylobatidea, All known Homo spp.] The majority of extinct taxa within the Hominini [DD: Hominoidea] were [DD: arboreal]
    bipedal, but the degree to which they were bipedal remains the subject of considerable debate. The significant discoveries of fossil hominin remains in the last 40 years have resulted in this debate becoming increasingly focused on how bipedal certain
    fossil taxa were, rather than on the overall process. Although the early hominin fossil record remains poor, evidence points to at least two distinct adaptive shifts. First, there was a shift to habitual [DD: arboreal] bipedalism, as typified by certain
    members of Australopithecus, but possibly including earlier genera such as Ardipithecus and Orrorin. Such taxa were [DD: arboreal] bipedal, but also retained a number of significant adaptations to arboreal climbing. The second shift was to fully obligate
    bipedalism [DD: Sifaka, Hylobatidae, Homo are all obligate bipeds.] and coincides with the emergence of the genus Homo [DD: No, of course not.]. By the Early Pleistocene, certain members of Homo had acquired a postcranial skeleton indicating fully
    humanlike striding bipedalism [DD: No chin so they must have had a different striding gait & weight distribution than modern humans]. The final part of this chapter reviews why bipedalism was selected for. [DD: Bipedalism long preceded the advent of Homo
    sapiens.] There have been many theoretical explanations, and the most robust remain those linked to the emergence of more varied habitats. Such an environmental shift would have involved strong selection for new behavioral strategies most likely linked
    to the efficient procurement of food. [DD: Such as better access to arboreal fruits and nuts]


    I mostly agree with DD, but IMO we should specify: early-hominoid BPism was less walking-climbing BPism than wading-climbing BPism: Miocene Hominoidea lived in swamp forests (most likely in coastal forests in S-Eurasia along the Tethys Ocean), where they
    frequently waded bipedally (upright) in the shallow water between the trees, and often climbed arms overhead in the branches above the water. This explains best in apes:
    -complete tail loss,
    -very broad sternum, thorax & pelvis + dorsal scapulas (also lateral movements of arms & legs),
    -centrally placed lumbar spine, with 5 rather than 7 lumbar vertebras, etc. This locomotion has been called (google) "aquarboreal" (aqua=water, arbor=tree).

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From Peter Nyikos@21:1/5 to marc verhaegen on Tue Mar 21 14:12:50 2023
    Thank you for reviving this thread, Marc. I hope you are still monitoring it, because I have a lot of comments to make on what Daud wrote, and on some that you added,
    and I'm curious to see what you think about them.

    You might not know that Daud announced here in s.b.p. about two
    months ago that he was taking a vacation from here and also from sci.anthropology.paleo.
    So don't expect any responses from him any time soon.

    On Friday, March 17, 2023 at 3:31:05 PM UTC-4, marc verhaegen wrote:
    Op dinsdag 22 november 2022 om 17:38:01 UTC+1 schreef Daud Deden:
    The Origins of Bipedal Locomotion
    William EH Harcourt-Smith 2013
    Handbook of PA doi 10.1007/978-3-642-27800-6_48-3
    Abstract
    Bipedalism is a highly specialized and unusual form of primate locomotion that is found today only in modern humans. [DD: Sifaka, Hylobatidea, All known Homo spp.]

    This was a very valid correction by Daud. I don't know whether he includes Indris or Avahis
    under "Sifaka", but they too are bipedal. There may be something about Madagascar, where
    all three of these other primates originated, that encourages bipedal locomotion.


    The majority of extinct taxa within the Hominini [DD: Hominoidea] were [DD: arboreal] bipedal,

    Here, OTOH, Daud was introducing a separate theme and not necessarily disagreeing.

    Do you see it that way too, Marc?

    but the degree to which they were bipedal remains the subject of considerable debate. The significant discoveries of fossil hominin remains in the last 40 years have resulted in this debate becoming increasingly focused on how bipedal certain fossil
    taxa were, rather than on the overall process. Although the early hominin fossil record remains poor, evidence points to at least two distinct adaptive shifts. First, there was a shift to habitual [DD: arboreal] bipedalism,

    Here, too, Daud was not necessarily disagreeing; here, though, he was adding details
    to the locomotion method rather than expanding the range of taxa.

    as typified by certain members of Australopithecus, but possibly including earlier genera such as Ardipithecus and Orrorin. Such taxa were [DD: arboreal] bipedal, but also retained a number of significant adaptations to arboreal climbing. The second
    shift was to fully obligate bipedalism [DD: Sifaka, Hylobatidae, Homo are all obligate bipeds.] and coincides with the emergence of the genus Homo [DD: No, of course not.].

    I'm not sure, but I think the author, William EH Harcourt-Smith, was only interested in the lineage
    leading up to Homo, and may have thought that bipedalism was independently acquired by
    Hylobatidae, as it seems to in the case of the lemurs mentioned above. Or he may have thought
    that bipedalism was temporarily lost in our lineage, and then regained.


    By the Early Pleistocene, certain members of Homo had acquired a postcranial skeleton indicating fully humanlike striding bipedalism [DD: No chin so they must have had a different striding gait & weight distribution than modern humans].

    I do not see how the word "must" is justified by "No chin." Do you, Marc?


    The final part of this chapter reviews why bipedalism was selected for. [DD: Bipedalism long preceded the advent of Homo sapiens.]

    See above about "lineage."


    There have been many theoretical explanations, and the most robust remain those linked to the emergence of more varied habitats. Such an environmental shift would have involved strong selection for new behavioral strategies most likely linked to the
    efficient procurement of food. [DD: Such as better access to arboreal fruits and nuts]


    Here is where you came in, Marc:

    I mostly agree with DD, but IMO we should specify: early-hominoid BPism was less walking-climbing BPism than wading-climbing BPism: Miocene Hominoidea lived in swamp forests (most likely in coastal forests in S-Eurasia along the Tethys Ocean),

    I've known about your wading-climbing hypothesis for over a year now, Marc, but
    I don't recall anything about the location. In fact, I just had Africa in the back of my
    mind when I read what you and Daud and Mario had written about it.

    It's an interesting amplification: is it possible that our lineage goes back to SE Asia before
    moving to Africa? or should I say, back to Africa? [Recall Proconsul and Ekembo, 17 to 20mya,
    predating Ramapithecus/Sivapithecus by about 5my.]


    where they frequently waded bipedally (upright) in the shallow water between the trees, and often climbed arms overhead in the branches above the water. This explains best in apes:
    -complete tail loss,
    -very broad sternum, thorax & pelvis + dorsal scapulas (also lateral movements of arms & legs),
    -centrally placed lumbar spine, with 5 rather than 7 lumbar vertebras, etc.

    Could you explain the connections? none of these suggests "aquarboreal" to me.


    This locomotion has been called (google) "aquarboreal" (aqua=water, arbor=tree).

    By you, yes, but here is what a search in google led to:

    https://groups.io/g/AAT/message/70711

    Jack, whoever he is, has trouble with the connections there. And your answers to him don't explain them.


    Peter Nyikos
    Professor, Dept. of Mathematics
    Univ. of South Carolina -- standard disclaimer-- http://people.math.sc.edu/nyikos

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)
  • From marc verhaegen@21:1/5 to All on Wed Mar 22 17:13:58 2023
    Op dinsdag 21 maart 2023 om 22:12:52 UTC+1 schreef Peter Nyikos:
    Thank you for reviving this thread, Marc. I hope you are still monitoring it,
    because I have a lot of comments to make on what Daud wrote, and on some that you added,
    and I'm curious to see what you think about them.
    You might not know that Daud announced here in s.b.p. about two
    months ago that he was taking a vacation from here and also from sci.anthropology.paleo.
    So don't expect any responses from him any time soon.

    OK, Peter.
    DD (Daud Deden) often has a lot of interesting thoughts.

    The Origins of Bipedal Locomotion
    William EH Harcourt-Smith 2013
    Handbook of PA doi 10.1007/978-3-642-27800-6_48-3
    Bipedalism is a highly specialized and unusual form of primate locomotion that is found today only in modern humans. [DD: Sifaka, Hylobatidea, All known Homo spp.]

    This was a very valid correction by Daud. I don't know whether he includes Indris or Avahis
    under "Sifaka", but they too are bipedal. There may be something about Madagascar, where
    all 3 of these other primates originated, that encourages bipedal locomotion.

    The majority of extinct taxa within the Hominini [DD: Hominoidea] were [DD: arboreal] bipedal,

    Here, OTOH, Daud was introducing a separate theme and not necessarily disagreeing.
    Do you see it that way too, Marc?

    The hominoid LCA was already "bipedal", but arboreality alone isn't enough to explain BPism.
    Since Primates are generally arboreal, and early-Pleistocene H.erectus was (semi)aquatic (his pachy-osteo-sclerosis is exclusively seen in slow+shallow-diving tetrapods), there must have been (since evolution is gradual) an intermediate phase of trees+
    water = aquarboreal (aqua=water, arbor=tree). AFAIR, I proposed this in 1990 or so, and a few years later, the wading gorillas of Ndoki were discovered (& later also wading bonobos & orangutans :-)). Aquarboreality IMO best explains why apes (vs monkeys)
    are more vertical, have less lumbar vertebras, a more centrally-placed lumbar spine, a very broad sternum (Hominoidea=Latisternalia) & thorax, placing the scapulas more dorsally (allowing more lateral movements of the arms), lost the tail (very
    unexpected in fast-moving purely arboreal mammals), climbed arms overhead (in the branches above the water) etc.

    but the degree to which they were bipedal remains the subject of considerable debate. The significant discoveries of fossil hominin remains in the last 40 years have resulted in this debate becoming increasingly focused on how bipedal certain
    fossil taxa were, rather than on the overall process. Although the early hominin fossil record remains poor, evidence points to at least 2 distinct adaptive shifts. First, there was a shift to habitual [DD: arboreal] bipedalism,

    Here, too, Daud was not necessarily disagreeing; here, though, he was adding details
    to the locomotion method rather than expanding the range of taxa.

    Miocene Hominoidea were very "bipedal"(aquarboreal) IMO: they spent a lot (even most?) time wading?

    as typified by certain members of Australopithecus, but possibly including earlier genera such as Ardipithecus and Orrorin. Such taxa were [DD: arboreal] bipedal, but also retained a number of significant adaptations to arboreal climbing. The
    second shift was to fully obligate bipedalism [DD: Sifaka, Hylobatidae, Homo are all obligate bipeds.] and coincides with the emergence of the genus Homo [DD: No, of course not.].

    I'm not sure, but I think the author, William EH Harcourt-Smith, was only interested in the lineage
    leading up to Homo, and may have thought that bipedalism was independently acquired by
    Hylobatidae, as it seems to in the case of the lemurs mentioned above. Or he may have thought
    that bipedalism was temporarily lost in our lineage, and then regained.

    Sifakas = hopping BPism, cf. kangaroos = ex-arboreal?
    But gibbons-humans = striding BPism = ex-aquarboreal?

    By the Early Pleistocene, certain members of Homo had acquired a postcranial skeleton indicating fully humanlike striding bipedalism [DD: No chin so they must have had a different striding gait & weight distribution than modern humans].

    I do not see how the word "must" is justified by "No chin." Do you, Marc?

    No, I don't see what DD means here.
    Ou chin IMO results from the (mid?late-Pleist.) transition diving->wading (cf. horizontal->vertical), cf. also less projecting mid-face, reduced nose-size, more anterior foramen magnum, higher forehead & brain-skull, loss of platycephaly, longer legs,
    less wide pelvis etc.

    The final part of this chapter reviews why bipedalism was selected for. [DD: Bipedalism long preceded the advent of Homo sapiens.]> See above about "lineage."
    There have been many theoretical explanations, and the most robust remain those linked to the emergence of more varied habitats. Such an environmental shift would have involved strong selection for new behavioral strategies most likely linked to
    the efficient procurement of food. [DD: Such as better access to arboreal fruits and nuts]

    Here is where you came in, Marc:

    I mostly agree with DD, but IMO we should specify:
    early-hominoid BPism was less walking-climbing BPism than wading-climbing BPism?
    Miocene Hominoidea lived in swamp forests, esp. in coastal forests in S-Eurasia along the Tethys Ocean?

    I've known about your wading-climbing hypothesis for over a year now, Marc, but
    I don't recall anything about the location. In fact, I just had Africa in the back of my
    mind when I read what you and Daud and Mario had written about it.

    My book "De evolutie van de mens" (Acad.Uitg. Eburon 2022 Utrecht NL) p.299-300:
    plate tectonics & hominoid splittings: hypothesis in short, schematically:
    -c 30-25 Ma India approaches S-Asia -> archipel fm = islands + coastal forests++ in Tethys Ocean:
    some Catarrhini reaching these coastal forests evolved -> aquarboreal Hominoidea,
    -c 20 Ma Ma India underneath Eurasia split lesser hylobatids(East) & great apes (West -> Tethys Sea),
    -c 15 Ma Mesopotamian Seaway closure split pongids-sivapiths East & hominids-dryopiths West,
    most died out late-Miocene, except in (incipient then) Red Sea: hominids s.s. (today Gorilla-Homo-Pan),
    -c 8 Ma northern Rift fm -> Afar: Gorilla -> Praeanthropus afarensis late-Miocene -> boisei early-Pleist. etc.
    -c 5 Ma Red Sea opened into Gulf (Francesca Mansfield: caused by Zanclean mega-flood 5.33 Ma):
    Pan -> right -> E.Afr.coast -> southern Rift -> Transvaal: Au.africanus late-Mio-> robustus early-Pleist. (// Gorilla),
    Homo -> left -> S.Asian coast -> Java -> + shellfish-diving ?early-Pleist.H.erectus = "aq.ape" s.s.: shellfish?

    IOW, schematically:
    Mio-Pliocene aquarboreal Hominoidea
    early-Pleist. predom.diving H.erectus
    mid-Pleist. diving+wading (e.g. H.neand. seasonally along rivers following salmon??)
    late-Pleist. wading-walking H.sapiens?


    It's an interesting amplification: is it possible that our lineage goes back to SE Asia before
    moving to Africa? or should I say, back to Africa? [Recall Proconsul and Ekembo, 17 to 20 mya,
    predating Ramapithecus/Sivapithecus by about 5my.]

    Yes, Out-of-Africa = empty slogan IMO: we come from S-Asia...

    where they frequently waded bipedally (upright) in the shallow water between the trees, and often climbed arms overhead in the branches above the water. This explains best in apes:
    -complete tail loss,
    -very broad sternum, thorax & pelvis + dorsal scapulas (also lateral movements of arms & legs),
    -centrally placed lumbar spine, with 5 rather than 7 lumbar vertebras, etc.

    Could you explain the connections? none of these suggests "aquarboreal" to me.

    No?? Swamp?coastal forest: quadrupal->BP = upright:
    -- head above the water,
    -- climbing arms overhead in the branches above the water!

    This locomotion has been called (google) "aquarboreal" (aqua=water, arbor=tree).

    By you, yes, but here is what a search in google led to: https://groups.io/g/AAT/message/70711
    Jack, whoever he is, has trouble with the connections there. And your answers to him don't explain them.
    Peter Nyikos Professor, Dept. of Mathematics
    Univ. of South Carolina -- standard disclaimer-- http://people.math.sc.edu/nyikos

    That's Gareth's opinion, but imagine a wading hominoid (e.g. collecting mangrove oysters??):
    his tail has no function AFAICS, only drag & infection-risk?

    Google "GondwanaTalks Verhaegen English" (or better: read my book...).
    My hypothesis "plate tectonics = hominoid splittings" is recent, just in time for my book: appendix 16:
    "Bijlage 16: "Platentektoniek en Hominoïde Opdelingen?" :-)
    These are in fact different hypotheses,
    - I'm pretty sure of Gorilla (Lucy in the N-Rift) // Pan (Taung in the S-Rift) and Pliocene Homo along the S-Asian coast,
    - but a bit less sure about hominid/pongid = Mesopot.Seaway closure,
    - and even less about India approaching S-Euasia = OWM/ape & lesser/gr.ape splits?

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)