• Upright posture for accessing leaves, not fruit, in open woodlands 21 m

    From Primum Sapienti@21:1/5 to All on Thu May 11 23:12:07 2023
    https://www.science.org/doi/10.1126/science.abq2835
    The evolution of hominoid locomotor versatility:
    Evidence from Moroto, a 21 Ma site in Uganda
    MacLatchy et al., Science 380, 172 (2023 14 April 2023


    INTRODUCTION:
    Inherent in traditional views of ape origins is the
    idea that, like living apes, early large-bodied apes
    lived in tropical forests. In response to constraints
    related to locomoting in forest canopies, it has been
    proposed that early apes evolved their quintessential
    upright torsos and acrobatic climbing and suspensory
    abilities, enhancing their locomotor versatility, to
    distribute their weight among small supports and thus
    reach ripe fruit in the terminal branches. This
    feeding and locomotor transition from a quadruped
    with a horizontal torso is thought to have occurred
    in the Middle Miocene due to an increasingly seasonal
    climate and feeding competition from evolving monkeys.
    ...

    RESULTS: A short, strong femur biomechanically
    favorable to vertical climbing and a vertebra
    indicating a dorsostable lower back
    confirmthat ape fossils fromMoroto II shared
    locomotor traits with living apes. Both
    Morotopithecus and a smaller ape from the
    site have elongated molars with well-developed
    crests for shearing leaves. Carbon isotopic
    signatures of the enamel of these apes and of
    other fossil mammals indicate that some mammals
    consistently fed onwater-stressedC3 plants,
    and possibly also C4 vegetation, in a woodland
    setting. Carbon isotope values of pedogenic
    carbonates, paleosol organic matter, and plant
    waxes all point to substantial C4 grass biomass
    on the landscape. Analysis of paleosols also
    indicates subhumid, strongly seasonal rainfall,
    and phytolith assemblages include forms from
    both aridadapted C4 grasses and forest-indicator
    plants.

    CONCLUSION: The ancient co-occurrence of
    dental specializations for leaf eating, rather
    than ripe fruit consumption, along with apelike
    locomotor abilities counters the predictions
    of the terminal branch forest frugivory
    hypotheses. The combined paleoecological
    evidence situates Morotopithecus in a woodland
    with a broken canopy and substantial
    grass understory including C4 species. These
    findings call for a new paradigm for the
    evolutionary origins of early apes. We propose
    that seasonal, wooded environments may have
    exerted previously unrecognized selective
    pressures in the evolution of arboreal apes.
    For example, some apes may have needed to
    access leaves in the higher canopy in times of
    low fruit availability and to be adept at
    ascending and descending from trees that lacked
    a continuous canopy.


    Abstract
    Living hominoids are distinguished by upright
    torsos and versatile locomotion. It is
    hypothesized that these features evolved for
    feeding on fruit from terminal branches in
    forests. To investigate the evolutionary context
    of hominoid adaptive origins, we analyzed
    multiple paleoenvironmental proxies in
    conjunction with hominoid fossils from the
    Moroto II site in Uganda. The data indicate
    seasonally dry woodlands with the earliest
    evidence of abundant C4 grasses in Africa based
    on a confirmed age of 21 million years ago (Ma).
    We demonstrate that the leaf-eating hominoid
    Morotopithecus consumed water-stressed
    vegetation, and postcrania from the site
    indicate ape-like locomotor adaptations. These
    findings suggest that the origin of hominoid
    locomotor versatility is associated with
    foraging on leaves in heterogeneous, open
    woodlands rather than forests.

    "Compositionally, this assemblage has affinities
    with modern phytolith assemblages fromwooded
    grasslands, but it is also consistent with open
    forests containing a substantial grass understory
    (e.g., riparian forest in a savanna landscape,
    dry forest, or forest openings)."

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  • From littoral.homo@gmail.com@21:1/5 to All on Fri May 12 03:49:43 2023
    Xth fantasy:

    https://www.science.org/doi/10.1126/science.abq2835
    The evolution of hominoid locomotor versatility:
    Evidence from Moroto, a 21 Ma site in Uganda
    MacLatchy et al., Science 380, 172 (2023 14 April 2023
    Inherent in traditional views of ape origins is the
    idea that, like living apes, early large-bodied apes
    lived in tropical forests. In response to constraints
    related to locomoting in forest canopies, it has been
    proposed that early apes evolved their quintessential
    upright torsos and acrobatic climbing and suspensory
    abilities, enhancing their locomotor versatility, to
    distribute their weight among small supports and thus
    reach ripe fruit in the terminal branches. This
    feeding and locomotor transition from a quadruped
    with a horizontal torso is thought to have occurred
    in the Middle Miocene due to an increasingly seasonal
    climate and feeding competition from evolving monkeys.

    IOW, just-so musings on some Miocene African catarrhine fossil.
    Great & lesser apes already split *early*Miocene,
    probably somewhere in S-Asia
    (I'd think in India: my book p.299, google "gondwanatalks vehaegen" https://www.gondwanatalks.com/l/the-waterside-hypothesis-wading-led-to-upright-walking-in-early-humans/).

    RESULTS: A short, strong femur biomechanically
    favorable to vertical climbing and a vertebra
    indicating a dorsostable lower back

    ??
    based on??

    confirm that ape fossils from Moroto II shared
    locomotor traits with living apes.

    A lot of Miocene primates might evolved some convergence with hominoids.

    Both
    Morotopithecus and a smaller ape from the
    site have elongated molars with well-developed
    crests for shearing leaves. Carbon isotopic
    signatures of the enamel of these apes and of
    other fossil mammals indicate that some mammals
    consistently fed on water-stressed C3 plants,
    and possibly also C4 vegetation, in a woodland
    setting. Carbon isotope values of pedogenic
    carbonates, paleosol organic matter, and plant
    waxes all point to substantial C4 grass biomass
    on the landscape. Analysis of paleosols also
    indicates subhumid, strongly seasonal rainfall,
    and phytolith assemblages include forms from
    both arid adapted C4 grasses and forest-indicator
    plants.
    CONCLUSION: The ancient co-occurrence of
    dental specializations for leaf eating, rather
    than ripe fruit consumption, along with apelike

    ??
    :-DDD
    Apes have
    -- no tail,
    -- 4 or 5 lumbar vertebras,
    -- broad sternum (Latisternalia),
    -- ...

    locomotor abilities counters the predictions
    of the terminal branch forest frugivory
    hypotheses. The combined paleoecological
    evidence situates Morotopithecus in a woodland
    with a broken canopy and substantial
    grass understory including C4 species. These
    findings call for a new paradigm for the
    evolutionary origins of early apes. We propose
    that seasonal, wooded environments may have
    exerted previously unrecognized selective
    pressures in the evolution of arboreal apes.
    For example, some apes may have needed to
    access leaves in the higher canopy in times of
    low fruit availability and to be adept at
    ascending and descending from trees that lacked
    a continuous canopy.
    Abstract
    Living hominoids are distinguished by upright
    torsos and versatile locomotion. It is
    hypothesized that these features evolved for
    feeding on fruit from terminal branches in
    forests. To investigate the evolutionary context
    of hominoid adaptive origins, we analyzed
    multiple paleoenvironmental proxies in
    conjunction with hominoid fossils from the
    Moroto II site in Uganda. The data indicate
    seasonally dry woodlands with the earliest
    evidence of abundant C4 grasses in Africa based
    on a confirmed age of 21 million years ago (Ma).
    We demonstrate that the leaf-eating hominoid
    Morotopithecus consumed water-stressed
    vegetation, and postcrania from the site
    indicate ape-like locomotor adaptations. These
    findings suggest that the origin of hominoid
    locomotor versatility is associated with
    foraging on leaves in heterogeneous, open
    woodlands rather than forests.
    "Compositionally, this assemblage has affinities
    with modern phytolith assemblages fromwooded
    grasslands, but it is also consistent with open
    forests containing a substantial grass understory
    (e.g. riparian forest in a savanna landscape,
    dry forest, or forest openings)."

    IOW, Morotopithecus was probably not hominoid:
    probably above-brancher with 6 or 7 lumbar vertebras.

    Most likely, Hominoidea originated in S-Asia:
    most hominoids in SE.Asia: siamangs & gibbons,
    pongids also in SE.Asia,
    Homo worldwide (H.erectus Java),
    only Pan & Gorilla in Africa.

    Discussion of Morotopith cs in my book p.72-74:
    Ugandapithecus (22–15 Ma), ontdekt bij fossiele krokodillen, waterschildpadden en waterdwerghertjes (Dorcatherium), wordt nu onderscheiden van Proconsul (Pickford 2009, Senut 2016): ze waren vaak veel groter (U.major-mannen tot 90 kg), allicht al
    rechtop klimmend, met een lang vlak gelaat, baviaan-grote hersenen, brede middenste bovensnijtanden, steviger hoektanden, en op de kiezen rondere knobbels met soms gerimpeld glazuur (planteneten?) en kenmerken die wat deden denken aan latere mensapen in
    Ethiopië en Kenya (Chorora-, Nakali- en Samburupithecus ~10 Ma) – en in sommige reconstructies, voor zover ik kan zien, ook aan Moroto~Afro~Heliopithecus:
    Morotopithecus (~21 Ma? ~40 kg) had een groot gebit en schedel gelijkend op Afro- en Heliopithecus hieronder: brede neus, grote kaakholtes, lang gelaat met een lange rij kiezen met dik kiesglazuur (met kammen voor bladeten, denkt Laura MacLatchy),
    vooruitstekende snijtanden en massieve hoektanden (maar zonder Afropithecus' saki-achtige specialisatie, zegt Andrew Deane). De dijbotkop was ‘primitief’ zoals bij hondapen (boventakkers), maar de dijschacht was kort en uitzonderlijk zwaar (nog
    zwaarder dan bij lori’s en orangs, trage hangklimmers – erg zware pootbotten zie je bij zeeotters, nijlpaarden en Pakicetus, een vermoedelijk-wadende oerwalvis). Er waren blijkbaar 7 of 6 lendenwervels zoals bij de meeste apen en Proconsul (mensen en
    gibbons ~5, grote-mensapen ~4), maar de erg ‘lage’ lendenwervels, de lange doornuitsteeksels achteraan de wervels, en de zoals bij ons naar achteren opgeschoven stevige dwarsuitsteeksels (processus transversi, Sanders 1993) doen denken aan een stijf
    opgerichte romp, voor tweebenigheid volgens Aaron Filler – ik denk verticaal klimmen en waden en misschien drijven in waterbos. De begeleidende fauna wees op een soort dambo, zegt Brigitte Senut: drasland vol biezen en zeggen, dat in het natte seizoen
    sterk onderwater staat. Martin Pickford twijfelt of de zware dijbotten en ‘moderne’ wervels wel bij de schedel horen, en volgens Masato Nakatsukasa leek het dwarsuitsteeksel onafhankelijk van ons naar achteren verschoven (in parallel), of varieerde
    de plaatsing van wervel tot wervel.
    Afropithecus (~16 Ma) geleek op Morotopithecus, lag ook bij waterdwerghertjes, varieerde ook sterk in gewicht, had een erg lang gelaat, zoals sommige veel vroegere en kleinere Fayyūm-apen (Aegyptopithecus, Saadanius), met ondiep verhemelte, grote, brede,
    spatelvormige, vooruitstekende bovensnijtanden, de middenste veel groter dan de tweede (zoals bij orangs), rechthoekige tandenboog en heel forse kiezen met nogal dik gerimpeld glazuur en afgeronde knobbels (bunodont). Hun sterke hoektanden waren saki-
    achtig (sclerocarp): kraakten ze harde vruchtdoppen? Hun ovale oogkassen, stevig omrand, stonden opvallend uiteen: hielpen grote neusholtes hun ogen, mond en neusgaten boven water? Ze leken nog vooral boventakkers, met forse grijphanden, volgens sommigen
    in tropische bossen met bladverlies in het droge seizoen. De iets kleinere ‘Saudi Ape’ (Helio- of Afropithecus leakeyi 18 of 17 Ma) lag in tropische kustafzettingen van de zuidelijke Tethys, nu de Perzische Golf.

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  • From JTEM is so reasonable@21:1/5 to All on Fri May 12 13:07:26 2023
    This is just stupid.

    Bipedalism is older than the LCA. You're claiming that the same
    environment that spawned bipedalism also destroyed it.

    Why? Explain this massive contradiction that makes you look
    stupid.




    -- --

    https://jtem.tumblr.com/post/717065307257176065

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