Atypical tooth wear found in fossil hominins also present in a Japanese macaque population
Ian Towle cs 2022 doi org/10.1002/ajpa.24500
Atypical tooth-wear incl. macroscopically visible striations on anterior teeth & within root grooves on posterior teeth are often regarded as evidence of non-masticatory, tool-use behavior in fossil hominins.
Both these types of dental tissue loss are often
- considered unique to the genus Homo,
- suggested to be the earliest evidence of human cultural habits.
We aim to
- describe similar tooth-wear found in a wild primate population,
- conduct a differential diagnosis of this atypical tissue loss.
Wild Jap.macaques (Koshima Island) were provisioned regularly on the beach (part of one of the longest-running primate field-sites).
Tooth-wear & -fractures in this group were compared to 2 other non-provisioned populations.
Infm on diet & behavior were obtained from extensive literature & on-going field-observations.
Results:
All Koshima Island individuals analyzed showed atypical tooth-wear:
- Large macroscopic striations were visible on many teeth,
sub-vertical striations were prominent on the labial surfaces of incisors.
- Root grooves on posterior teeth were observed in half of the individuals, some showed clear directional striations similar to “tooth-pick” grooves in fossil hominins.
- Tool-use & the habitual insertion of non-masticatory items in the mouth has not been observed in this population.
Concl.
Accidental ingestion of sand & oral processing of marine mollusks likely creates these atypical wear patterns.
Implications for similar wear that has been ass.x tool-use in fossil hominin samples were discussed.
Atypical tooth wear found in fossil hominins also present in a Japanese macaque population
Ian Towle cs 2022 doi org/10.1002/ajpa.24500
Atypical tooth-wear incl. macroscopically visible striations on anterior teeth & within root grooves on posterior teeth are often regarded as evidence of non-masticatory, tool-use behavior in fossil hominins.
Both these types of dental tissue loss are often
- considered unique to the genus Homo,
- suggested to be the earliest evidence of human cultural habits.
We aim to
- describe similar tooth-wear found in a wild primate population,
- conduct a differential diagnosis of this atypical tissue loss.
Wild Jap.macaques (Koshima Island) were provisioned regularly on the beach (part of one of the longest-running primate field-sites).
Tooth-wear & -fractures in this group were compared to 2 other non-provisioned populations.
Infm on diet & behavior were obtained from extensive literature & on-going field-observations.
Results:
All Koshima Island individuals analyzed showed atypical tooth-wear:
- Large macroscopic striations were visible on many teeth,
sub-vertical striations were prominent on the labial surfaces of incisors. - Root grooves on posterior teeth were observed in half of the individuals,
some showed clear directional striations similar to “tooth-pick” grooves in fossil hominins.
- Tool-use & the habitual insertion of non-masticatory items in the mouth has not been observed in this population.
Concl.
Accidental ingestion of sand & oral processing of marine mollusks likely creates these atypical wear patterns.
Implications for similar wear that has been ass.x tool-use in fossil hominin samples were discussed.
Well, what can I say, finally. Thanks Marc.
I would laugh uncontrollably, but recently I heard about Victorian etiquette, so I will just chuckle ...heh...heh...heh.
Op donderdag 31 augustus 2023 om 21:01:40 UTC+2 schreef Mario Petrinovic: Thanks, Mario, at least 8 independent facts indicate that Indonesian erectus frequently dived or shellfish:
• Archaic Homo's atypical tooth-wear was caused by "sand & oral processing of marine mollusks", Towle cs 2022 https://onlinelibrary.wiley.com/doi/10.1002/ajpa.24500
•H.erectus s.s. fossilized typically (always?) in coastal sediments, e.g. Mojokerto amid barnacles & corals, Trinil amid Pseudodon & Elongaria, Sangiran-17 in "brackish marsh near the coast".
•Stephen Munro discovered sea-shell engravings made by H.erectus, Joordens cs 2015 Nature 518:228–231 https://pubmed.ncbi.nlm.nih.gov/25470048/
•Ear exostoses (H.erectus & H.neand.) develop after years of cold(er) water irrigation https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5696936/
•Pachyosteosclerosis is typically & exclusively seen in slow+shallow-diving tetrapods (de Buffrénil cs 2010 J.Mamm.Evol.17:101-120), e.g. erectus’ parietal bone is 2x as thick as in gorillas.
•Brain size in erectus (2x apes & australopiths) is facilitated by sea-food, e.g. DHA docosahexaenoic acid in shellfish etc., e.g. Odontocetes, Pinnipedia.
•Pleistocene Homo even colonized overseas islands (Flores & later even Luzon) https://www.academia.edu/36193382/Coastal_Dispersal_of_Pleistocene_Homo_2018
•Homo’s stone tool use & dexterity is typical for molluscivores, cf. sea-otters etc.
Only complete idiots still belieeve their Pleistocene ancestors ran over Afr.savannas after antelopes...
Atypical tooth wear found in fossil hominins also present in a Japanese macaque population
Ian Towle cs 2022 doi org/10.1002/ajpa.24500
Atypical tooth-wear incl. macroscopically visible striations on anterior teeth & within root grooves on posterior teeth are often regarded as evidence of non-masticatory, tool-use behavior in fossil hominins.
Both these types of dental tissue loss are often
- considered unique to the genus Homo,
- suggested to be the earliest evidence of human cultural habits.
We aim to
- describe similar tooth-wear found in a wild primate population,
- conduct a differential diagnosis of this atypical tissue loss.
Wild Jap.macaques (Koshima Island) were provisioned regularly on the beach (part of one of the longest-running primate field-sites).
Tooth-wear & -fractures in this group were compared to 2 other non-provisioned populations.
Infm on diet & behavior were obtained from extensive literature & on-going field-observations.
Results:
All Koshima Island individuals analyzed showed atypical tooth-wear:
- Large macroscopic striations were visible on many teeth,
sub-vertical striations were prominent on the labial surfaces of incisors. >>> - Root grooves on posterior teeth were observed in half of the individuals, >>> some showed clear directional striations similar to “tooth-pick” grooves in fossil hominins.
- Tool-use & the habitual insertion of non-masticatory items in the mouth has not been observed in this population.
Concl.
Accidental ingestion of sand & oral processing of marine mollusks likely creates these atypical wear patterns.
Implications for similar wear that has been ass.x tool-use in fossil hominin samples were discussed.
Well, what can I say, finally. Thanks Marc.
I would laugh uncontrollably, but recently I heard about Victorian
etiquette, so I will just chuckle ...heh...heh...heh.
Thanks, Mario, at least 8 independent facts indicate that Indonesian erectus frequently dived or shellfish:
• Archaic Homo's atypical tooth-wear was caused by "sand & oral processing of marine mollusks", Towle cs 2022 https://onlinelibrary.wiley.com/doi/10.1002/ajpa.24500
•H.erectus s.s. fossilized typically (always?) in coastal sediments, e.g. Mojokerto amid barnacles & corals, Trinil amid Pseudodon & Elongaria, Sangiran-17 in "brackish marsh near the coast".
•Stephen Munro discovered sea-shell engravings made by H.erectus, Joordens cs 2015 Nature 518:228–231 https://pubmed.ncbi.nlm.nih.gov/25470048/
•Ear exostoses (H.erectus & H.neand.) develop after years of cold(er) water irrigation https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5696936/
•Pachyosteosclerosis is typically & exclusively seen in slow+shallow-diving tetrapods (de Buffrénil cs 2010 J.Mamm.Evol.17:101-120), e.g. erectus’ parietal bone is 2x as thick as in gorillas.
•Brain size in erectus (2x apes & australopiths) is facilitated by sea-food, e.g. DHA docosahexaenoic acid in shellfish etc., e.g. Odontocetes, Pinnipedia.
•Pleistocene Homo even colonized overseas islands (Flores & later even Luzon) https://www.academia.edu/36193382/Coastal_Dispersal_of_Pleistocene_Homo_2018
•Homo’s stone tool use & dexterity is typical for molluscivores, cf. sea-otters etc.
Only complete idiots still belieeve their Pleistocene ancestors ran over Afr.savannas after antelopes...
Atypical tooth wear found in fossil hominins also present in a Japanese macaque population
Ian Towle cs 2022 doi org/10.1002/ajpa.24500
Atypical tooth-wear incl. macroscopically visible striations on anterior teeth & within root grooves on posterior teeth are often regarded as evidence of non-masticatory, tool-use behavior in fossil hominins.
Both these types of dental tissue loss are often
- considered unique to the genus Homo,
- suggested to be the earliest evidence of human cultural habits.
We aim to
- describe similar tooth-wear found in a wild primate population,
- conduct a differential diagnosis of this atypical tissue loss.
Wild Jap.macaques (Koshima Island) were provisioned regularly on the beach (part of one of the longest-running primate field-sites).
Tooth-wear & -fractures in this group were compared to 2 other non-provisioned populations.
Infm on diet & behavior were obtained from extensive literature & on-going field-observations.
Results:
All Koshima Island individuals analyzed showed atypical tooth-wear:
- Large macroscopic striations were visible on many teeth,
sub-vertical striations were prominent on the labial surfaces of incisors.
- Root grooves on posterior teeth were observed in half of the individuals,
some showed clear directional striations similar to “tooth-pick” grooves in fossil hominins.
- Tool-use & the habitual insertion of non-masticatory items in the mouth has not been observed in this population.
Concl.
Accidental ingestion of sand & oral processing of marine mollusks likely creates these atypical wear patterns.
Implications for similar wear that has been ass.x tool-use in fossil hominin samples were discussed.
Well, what can I say, finally. Thanks Marc.
I would laugh uncontrollably, but recently I heard about Victorian
etiquette, so I will just chuckle ...heh...heh...heh.
H. floresiensis has small brain.
Op vrijdag 1 september 2023 om 00:26:13 UTC+2 schreef Mario Petrinovic:
Thanks, Mario, at least 8 independent facts indicate that Indonesian erectus frequently dived or shellfish:
• Archaic Homo's atypical tooth-wear was caused by "sand & oral processing of marine mollusks", Towle cs 2022 https://onlinelibrary.wiley.com/doi/10.1002/ajpa.24500
•H.erectus s.s. fossilized typically (always?) in coastal sediments, e.g. Mojokerto amid barnacles & corals, Trinil amid Pseudodon & Elongaria, Sangiran-17 in "brackish marsh near the coast".
•Stephen Munro discovered sea-shell engravings made by H.erectus, Joordens cs 2015 Nature 518:228–231 https://pubmed.ncbi.nlm.nih.gov/25470048/
•Ear exostoses (H.erectus & H.neand.) develop after years of cold(er) water irrigation https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5696936/
•Pachyosteosclerosis is typically & exclusively seen in slow+shallow-diving tetrapods (de Buffrénil cs 2010 J.Mamm.Evol.17:101-120), e.g. erectus’ parietal bone is 2x as thick as in gorillas.
•Brain size in erectus (2x apes & australopiths) is facilitated by sea-food, e.g. DHA docosahexaenoic acid in shellfish etc., e.g. Odontocetes, Pinnipedia.
•Pleistocene Homo even colonized overseas islands (Flores & later even Luzon) https://www.academia.edu/36193382/Coastal_Dispersal_of_Pleistocene_Homo_2018
•Homo’s stone tool use & dexterity is typical for molluscivores, cf. sea-otters etc.
Only complete idiots still belieeve their Pleistocene ancestors ran over Afr.savannas after antelopes...
Atypical tooth wear found in fossil hominins also present in a Japanese macaque population
Ian Towle cs 2022 doi org/10.1002/ajpa.24500
Atypical tooth-wear incl. macroscopically visible striations on anterior teeth & within root grooves on posterior teeth are often regarded as evidence of non-masticatory, tool-use behavior in fossil hominins.
Both these types of dental tissue loss are often
- considered unique to the genus Homo,
- suggested to be the earliest evidence of human cultural habits.
We aim to
- describe similar tooth-wear found in a wild primate population,
- conduct a differential diagnosis of this atypical tissue loss.
Wild Jap.macaques (Koshima Island) were provisioned regularly on the beach (part of one of the longest-running primate field-sites).
Tooth-wear & -fractures in this group were compared to 2 other non-provisioned populations.
Infm on diet & behavior were obtained from extensive literature & on-going field-observations.
Results:
All Koshima Island individuals analyzed showed atypical tooth-wear:
- Large macroscopic striations were visible on many teeth,
sub-vertical striations were prominent on the labial surfaces of incisors.
- Root grooves on posterior teeth were observed in half of the individuals,
some showed clear directional striations similar to “tooth-pick” grooves in fossil hominins.
- Tool-use & the habitual insertion of non-masticatory items in the mouth has not been observed in this population.
Concl.
Accidental ingestion of sand & oral processing of marine mollusks likely creates these atypical wear patterns.
Implications for similar wear that has been ass.x tool-use in fossil hominin samples were discussed.
Well, what can I say, finally. Thanks Marc.
I would laugh uncontrollably, but recently I heard about Victorian
etiquette, so I will just chuckle ...heh...heh...heh.
H. floresiensis has small brain.
Yes.
Island dwarfism??
Brain size of Homo floresiensis and its evolutionary implications
Daisuke Kubo cs 2013 doi org/10.1098/rspb.2013.0338
The extremely small endocranial volume ECV of LB1 (Hf type-spm) poses a challenge in our understanding of human brain evolution:
- some hypothesize dramatic dwarfing of rel.ECV from He, presumably without significant decrease in intellectual function,
- others expect a lesser degree of brain diminution from a more primitive, small-brained form of hominin, currently undocumented in E-Asia.
But uncertainties are, e.g.
-inconsistency in the published ECVs for LB1 (380–430 cc),
-unclear human intra-specific brain–body size scaling.
We accurately determine the ECV of LB1, using high-resolution micro-CT scan. The ECV (426 cc) is larger than the commonly cited figure in previous studies (400 cc).
Coupled with Hs brain–body size correlation (calculated based on a sample from 20 worldwide modern populations), we construct new models of the ECV reduction in Hf evolution.
Result: a more significant contribution of scaling effect than previously claimed.
Thanks, Mario, at least 8 independent facts indicate that Indonesian erectus frequently dived or shellfish:
• Archaic Homo's atypical tooth-wear was caused by "sand & oral processing of marine mollusks", Towle cs 2022 https://onlinelibrary.wiley.com/doi/10.1002/ajpa.24500
•H.erectus s.s. fossilized typically (always?) in coastal sediments, e.g. Mojokerto amid barnacles & corals, Trinil amid Pseudodon & Elongaria, Sangiran-17 in "brackish marsh near the coast".
•Stephen Munro discovered sea-shell engravings made by H.erectus, Joordens cs 2015 Nature 518:228–231 https://pubmed.ncbi.nlm.nih.gov/25470048/
•Ear exostoses (H.erectus & H.neand.) develop after years of cold(er) water irrigation https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5696936/
•Pachyosteosclerosis is typically & exclusively seen in slow+shallow-diving tetrapods (de Buffrénil cs 2010 J.Mamm.Evol.17:101-120), e.g. erectus’ parietal bone is 2x as thick as in gorillas.
•Brain size in erectus (2x apes & australopiths) is facilitated by sea-food, e.g. DHA docosahexaenoic acid in shellfish etc., e.g. Odontocetes, Pinnipedia.
•Pleistocene Homo even colonized overseas islands (Flores & later even Luzon) https://www.academia.edu/36193382/Coastal_Dispersal_of_Pleistocene_Homo_2018
•Homo’s stone tool use & dexterity is typical for molluscivores, cf. sea-otters etc.
Only complete idiots still belieeve their Pleistocene ancestors ran over Afr.savannas after antelopes...
Atypical tooth wear found in fossil hominins also present in a Japanese macaque population
Ian Towle cs 2022 doi org/10.1002/ajpa.24500
Atypical tooth-wear incl. macroscopically visible striations on anterior teeth & within root grooves on posterior teeth are often regarded as evidence of non-masticatory, tool-use behavior in fossil hominins.
Both these types of dental tissue loss are often
- considered unique to the genus Homo,
- suggested to be the earliest evidence of human cultural habits. >>>>> We aim to
- describe similar tooth-wear found in a wild primate population, >>>>> - conduct a differential diagnosis of this atypical tissue loss.
Wild Jap.macaques (Koshima Island) were provisioned regularly on the beach (part of one of the longest-running primate field-sites).
Tooth-wear & -fractures in this group were compared to 2 other non-provisioned populations.
Infm on diet & behavior were obtained from extensive literature & on-going field-observations.
Results:
All Koshima Island individuals analyzed showed atypical tooth-wear: >>>>> - Large macroscopic striations were visible on many teeth,
sub-vertical striations were prominent on the labial surfaces of incisors.
- Root grooves on posterior teeth were observed in half of the individuals,
some showed clear directional striations similar to “tooth-pick” grooves in fossil hominins.
- Tool-use & the habitual insertion of non-masticatory items in the mouth has not been observed in this population.
Concl.
Accidental ingestion of sand & oral processing of marine mollusks likely creates these atypical wear patterns.
Implications for similar wear that has been ass.x tool-use in fossil hominin samples were discussed.
Well, what can I say, finally. Thanks Marc.
I would laugh uncontrollably, but recently I heard about Victorian
etiquette, so I will just chuckle ...heh...heh...heh.
H. floresiensis has small brain.
Yes. > Island dwarfism??
Brain size of Homo floresiensis and its evolutionary implications
Daisuke Kubo cs 2013 doi org/10.1098/rspb.2013.0338
The extremely small endocranial volume ECV of LB1 (Hf type-spm) poses a challenge in our understanding of human brain evolution:
- some hypothesize dramatic dwarfing of rel.ECV from He, presumably without significant decrease in intellectual function,
- others expect a lesser degree of brain diminution from a more primitive, small-brained form of hominin, currently undocumented in E-Asia.
But uncertainties are, e.g.
-inconsistency in the published ECVs for LB1 (380–430 cc),
-unclear human intra-specific brain–body size scaling.
We accurately determine the ECV of LB1, using high-resolution micro-CT scan.
The ECV (426 cc) is larger than the commonly cited figure in previous studies (400 cc).
Coupled with Hs brain–body size correlation (calculated based on a sample from 20 worldwide modern populations), we construct new models of the ECV reduction in Hf evolution.
Result: a more significant contribution of scaling effect than previously claimed.
In my view, it is obvious that those guys are more primitive (so, no
island dwarfing), yet equally intelligent as we are. And thye are not
the only ones, we also have H.naledi (if I got it right). They are both
on southern edges of human range.
Simply, Marc, your thesis of pumping human brain by sea food is wrong.
It is the thermoregulatory thing.
"Homo naledi" was not Homo, of course, but Pan or Australopith.naledi,
Simply, Marc, your thesis of pumping human brain by sea food is wrong.*My* thesis??
I only see a correlation between aq.mammals & larger brains,
but why exactly why is still not fully understood AFAICS.
littor...@gmail.com wrote:
"Homo naledi" was not Homo, of course, but Pan or Australopith.naledi,
I immediately thought so myself.
I'm not even sure there's that massive a difference between
Pan and Australopithecus. I mean, look how close we are to
Pan NOW! Some argue that "Pan" doesn't even exist, and we
should be classifying them as Homo. A different species of
Homo but still Homo.
Anyway, erase millions of years of evolving apart and one
would presume that Pan and Australopithecus were a good
deal closer than we are to Pan...
Actually: I would suspect that Pan is Australopithecus after
expanding greatly -- it was a VERY successful genus, last I
heard -- only to become cut off, or isolated... last man standing,
so to speak. https://groups.google.com/g/sci.anthropology.paleo/c/VE486A_o7n4/m/KeOE4L9cBQAJ
Simply, Marc, your thesis of pumping human brain by sea food is wrong.
*My* thesis??
I only see a correlation between aq.mammals & larger brains,
but why exactly why is still not fully understood AFAICS.
Oh, it's a done deal. Our species is hooked on DHA, and that
could never have happened absent a diet very rich in DHA.
We need it. Period. And we're supposedly way better at synthesizing
it than any archaic ancestor was...
DHA is brain food.
Think of it like this: DHA doesn't magic into bigger brains. You
need selective pressures to grow bigger brains. But our
ancestors built those bigger brains in a large part with DHA,
so we were never going to get big brains without it.
DHA all by itself is proof of Aquatic Ape.
So isn't "Coastal Dispersal."
At this point all we're arguing about is WHEN it started, how
long it went on for and what exactly it contributed to human
evolution.
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