Its easy to dismiss something as 'tremendously absurd' as it avoids having to address the absurdity of the alternative (the imaginary centers of origin and contradictory dispersal stories). There is nothing objective about any particular gap between the fossil record and age of origin being 'far out'. It's just a personal opinion. Not science. Similarly there are no objective limits on this. There are examples of taxa having a fossil record extended by 100 Ma so its not unprecedented.
John Grehan
From: paleoanthropology@yahoogroups.com [mailto:paleoanthropology@yahoogroups.com] On Behalf Of Torfinn Ørmen Sent: Wednesday, December 02, 2009 6:37 PM To: paleoanthropology@yahoogroups.com Subject: Re: [paleoanthropology] primates in the Jurassic
The basic idea of appying tectonics to predicting zoogeographical patterns is interesting and has some merit. Regarding some animal groups. Over on vrtpaleo (an international maling list with mostly professional vertebrate zoologists and paleontologists) the pattern outlined in this paper was regarded as "tremendously absurd". To have strepsirhines and haplorhines separate in the Early Jurassic at 180 Ma seems a bit far out when the earliest fossil evidence for primitive placentals is from the Early Cretaceous (the Chinese Barremian, ap. 125 Ma)...
That being said, the author has a very valid point about the dangers of regarding the oldest fossil evidence as the absolute oldest occurrence of the lineage in question. But there are limits to how many 100 Ma ghost lines we can expect in _one_ mammal order.
Cheers
Torfinn
No, not a fossil, but new biogeographic evidence for primates, and major primate groups in the Jurassic and even anthropoids in the early Cretaceous. Abstract below of an article published in Zoologica Scripta that demonstrates how the patterns of distribution and diversity predict a Mesozoic differentiation of primates and put rest the otherwise contradictory and imaginative nonsense appealing to recent trans-oceanic dispersal to ‘explain’ monkeys in the New World and lemurs in Madagascar. Anyone interested in a pdf copy can request from me or the author.
This is a little outside paleoanthropology, but I anticipate some on this list might find the topic of interest.
John Grehan
Heads, M. Evolution and biogeography of primates: a new model based on molecular phylogenetics,
vicariance and plate tectonics. —Zoologica Scripta, **, ***–***.
The ages of the oldest fossils suggest an origin for primates in the Paleocene (_56 Ma).
Fossil-calibrated molecular clock dates give Cretaceous dates (_80–116 Ma). Both these
estimates are minimum dates although they are often ‘transmogrified’ and treated as maximum
or absolute dates. Oldest fossils can underestimate ages by tens of millions of years
and instead of calibrating the time-course of evolution with a scanty fossil record, the geographical
boundaries of the main molecular clades of primates are calibrated here with
radiometrically dated tectonic events. This indicates that primates originated when a globally
widespread ancestor (early Archonta) differentiated into a northern group (Plesiadapiformes,
extinct), a southern group (Primates), and two south-east Asian groups
(Dermoptera and Scandentia). The division occurred with the breakup of Pangea in the
Early Jurassic and the opening of the central Atlantic (_185 Ma). Within primates, the
strepsirrhines and haplorhines diverged with volcanism and buckling on the Lebombo
Monocline, a volcanic rifted margin in south-east Africa (Early Jurassic, _180 Ma). Within
strepsirrhines, lorises and galagos (Africa and Asia) and lemurs (Madagascar) diverged with
the formation of the Mozambique Channel (Middle Jurassic, _160 Ma). Within haplorhines,
Old World monkeys and New World monkeys diverged with the opening of the
Atlantic (Early Cretaceous, _130 Ma). The main aspects of primate distribution are interpreted
as the result of plate tectonics, phylogeny and vicariance, with some subsequent
range expansion leading to secondary overlap. Long-distance, trans-oceanic dispersal
events are not necessary. The primate ancestral complex was already widespread globally
when sea-floor spreading, strike-slip rifting and orogeny fractured and deformed distributions
through the Jurassic and Cretaceous, leading to the origin of the modern clades. The
model suggests that the topology of the phylogenetic tree reflects a sequence of differentiation
in a widespread ancestor rather than a series of dispersal events.
Corresponding author: Michael Heads, Buffalo Museum of Science, 1020 Humboldt Parkway,
Buffalo, NY14211-1293, USA. E-mail: michael.heads@yahoo.com
The basic idea of appying tectonics to predicting zoogeographical patterns is interesting and has some merit. Regarding some animal groups. Over on vrtpaleo (an international maling list with mostly professional vertebrate zoologists and paleontologists) the pattern outlined in this paper was regarded as "tremendously absurd". To have strepsirhines and haplorhines separate in the Early Jurassic at 180 Ma seems a bit far out when the earliest fossil evidence for primitive placentals is from the Early Cretaceous (the Chinese Barremian, ap. 125 Ma)...
That being said, the author has a very valid point about the dangers of regarding the oldest fossil evidence as the absolute oldest occurrence of the lineage in question. But there are limits to how many 100 Ma ghost lines we can expect in _one_ mammal order.
Cheers
Torfinn
No, not a fossil, but new biogeographic evidence for primates, and major primate groups in the Jurassic and even anthropoids in the early Cretaceous. Abstract below of an article published in Zoologica Scripta that demonstrates how the patterns of distribution and diversity predict a Mesozoic differentiation of primates and put rest the otherwise contradictory and imaginative nonsense appealing to recent trans-oceanic dispersal to ‘explain’ monkeys in the New World and lemurs in Madagascar. Anyone interested in a pdf copy can request from me or the author.
This is a little outside paleoanthropology, but I anticipate some on this list might find the topic of interest.
John Grehan
Heads, M. Evolution and biogeography of primates: a new model based on molecular phylogenetics,
vicariance and plate tectonics. —Zoologica Scripta, **, ***–***.
The ages of the oldest fossils suggest an origin for primates in the Paleocene (_56 Ma).
Fossil-calibrated molecular clock dates give Cretaceous dates (_80–116 Ma). Both these
estimates are minimum dates although they are often ‘transmogrified’ and treated as maximum
or absolute dates. Oldest fossils can underestimate ages by tens of millions of years
and instead of calibrating the time-course of evolution with a scanty fossil record, the geographical
boundaries of the main molecular clades of primates are calibrated here with
radiometrically dated tectonic events. This indicates that primates originated when a globally
widespread ancestor (early Archonta) differentiated into a northern group (Plesiadapiformes,
extinct), a southern group (Primates), and two south-east Asian groups
(Dermoptera and Scandentia). The division occurred with the breakup of Pangea in the
Early Jurassic and the opening of the central Atlantic (_185 Ma). Within primates, the
strepsirrhines and haplorhines diverged with volcanism and buckling on the Lebombo
Monocline, a volcanic rifted margin in south-east Africa (Early Jurassic, _180 Ma). Within
strepsirrhines, lorises and galagos (Africa and Asia) and lemurs (Madagascar) diverged with
the formation of the Mozambique Channel (Middle Jurassic, _160 Ma). Within haplorhines,
Old World monkeys and New World monkeys diverged with the opening of the
Atlantic (Early Cretaceous, _130 Ma). The main aspects of primate distribution are interpreted
as the result of plate tectonics, phylogeny and vicariance, with some subsequent
range expansion leading to secondary overlap. Long-distance, trans-oceanic dispersal
events are not necessary. The primate ancestral complex was already widespread globally
when sea-floor spreading, strike-slip rifting and orogeny fractured and deformed distributions
through the Jurassic and Cretaceous, leading to the origin of the modern clades. The
model suggests that the topology of the phylogenetic tree reflects a sequence of differentiation
in a widespread ancestor rather than a series of dispersal events.
Corresponding author: Michael Heads, Buffalo Museum of Science, 1020 Humboldt Parkway,
Buffalo, NY14211-1293, USA. E-mail: michael.heads@yahoo.com
No, not a fossil, but new biogeographic evidence for
primates, and major primate groups in the Jurassic and even anthropoids in the
early Cretaceous. Abstract below of an article published in Zoologica Scripta
that demonstrates how the patterns of distribution and diversity predict a
Mesozoic differentiation of primates and put rest the otherwise contradictory
and imaginative nonsense appealing to recent trans-oceanic dispersal to
‘explain’ monkeys in the New World and lemurs in Madagascar.
Anyone interested in a pdf copy can request from me or the author.
This is a little outside paleoanthropology, but I anticipate
some on this list might find the topic of interest.
John Grehan
Heads, M. Evolution and biogeography of primates: a new
model based on molecular phylogenetics,
vicariance and plate tectonics. —Zoologica Scripta,
**, ***–***.
The ages of the oldest fossils suggest an origin for
primates in the Paleocene (_56 Ma).
Fossil-calibrated molecular clock dates give Cretaceous
dates (_80–116 Ma). Both these
estimates are minimum dates although they are often
‘transmogrified’ and treated as maximum
or absolute dates. Oldest fossils can underestimate ages by
tens of millions of years
and instead of calibrating the time-course of evolution with
a scanty fossil record, the geographical
boundaries of the main molecular clades of primates are
calibrated here with
radiometrically dated tectonic events. This indicates that
primates originated when a globally
widespread ancestor (early Archonta) differentiated into a
northern group (Plesiadapiformes,
extinct), a southern group (Primates), and two south-east
Asian groups
(Dermoptera and Scandentia). The division occurred with the
breakup of Pangea in the
Early Jurassic and the opening of the central Atlantic (_185 Ma). Within primates, the
strepsirrhines and haplorhines diverged with volcanism and
buckling on the Lebombo
Monocline, a volcanic rifted margin in south-east Africa (Early Jurassic, _180 Ma). Within
strepsirrhines, lorises and galagos (Africa and Asia) and
lemurs (Madagascar)
diverged with
the formation of the Mozambique Channel
(Middle Jurassic, _160 Ma). Within haplorhines,
Old World monkeys and New World
monkeys diverged with the opening of the
Atlantic (Early Cretaceous, _130 Ma). The main aspects of
primate distribution are interpreted
as the result of plate tectonics, phylogeny and vicariance,
with some subsequent
range expansion leading to secondary overlap. Long-distance,
trans-oceanic dispersal
events are not necessary. The primate ancestral complex was
already widespread globally
when sea-floor spreading, strike-slip rifting and orogeny
fractured and deformed distributions
through the Jurassic and Cretaceous, leading to the origin
of the modern clades. The
model suggests that the topology of the phylogenetic tree
reflects a sequence of differentiation
in a widespread ancestor rather than a series of dispersal
events.
Corresponding author: Michael Heads, Buffalo Museum of
Science, 1020 Humboldt Parkway,
Buffalo, NY14211-1293,
USA. E-mail:
michael.heads@...
Department of Anthropology, Northern Illinois University, DeKalb, IL, USA. dgebo@...
New
early Miocene forelimb fossils have been recovered from the Songhor and
Lower Kapurtay localities in southwestern Kenya. We describe four
specimens that are similar in size and functional capabilities. Their
specific allocation is problematic but these forelimb specimens must
belong to either Rangwapithecus gordoni or Proconsul africanus. If
these new postcranial specimens should belong to R. gordoni, on the
basis of size and common dental specimens found at Songhor, they
represent a new elbow complex. The morphology of these fossils is
anatomically and functionally similar to that of Proconsul. The
proconsuloid elbow complex allows extensive forelimb rotations and is
capable of performing arboreal quadrupedalism and climbing activities.
No suspensory adaptations are apparent. The proconsuloid elbow complex
remains a good ancestral condition for hominoid primates.
Department of Anatomical Sciences, Stony Brook University, Stony Brook, NY 11794, USA.
Interpretations
of the postcranial anatomy of East African early and middle Miocene
large-bodied hominoids (e.g., Proconsul, Afropithecus, Turkanapithecus,
Nacholapithecus) have suggested that these diverse primates utilized
positional behaviors dominated by arboreal quadrupedalism. Preliminary
descriptions of the Equatorius africanus partial skeleton (KNM-TH
28860) and other forelimb specimens, however, have argued that this
animal relied more on terrestrial locomotion compared to its
contemporaries, possibly similar to extant large papionin monkeys. In
this paper, we reevaluate this interpretation by examining intrinsic
hand proportions based on the lengths of the third proximal phalanx and
fifth metacarpal in Equatorius in reference to a large sample of extant
catarrhine primate taxa. We focused on the lengths of these hand bones
because the ratio between phalanx and metacarpal lengths has been
previously documented to discriminate terrestrial from arboreal
mammalian taxa, including primates. The Equatorius hand displays
semi-terrestrial hand proportions with a relatively shorter proximal
phalanx compared to most arboreal monkeys. Its proximal phalanx,
however, is relatively longer than those of habitually terrestrial
monkeys (e.g., Theropithecus, Papio). Accordingly, although Equatorius
retains some arboreal quadrupedal characteristics, these results
corroborate the previous inference that it engaged in more terrestrial
locomotion than earlier Miocene apes such as Proconsul. We suggest that
the postcranial skeleton of Equatorius evinces the earliest signs of
semi-terrestriality in the hominoid fossil record. It is likely that
the terrestrial specialization utilized by living hominoids, e.g.,
knuckle-walking, evolved separately.
My mistake guys!
Marcel F. Williams
--- In paleoanthropology@yahoogroups.com, Marc Verhaegen <m_verhaegen@...>
wrote:
>
> Marcel, they say "adducted", not "abducted"!
>
> --marc
>
>
>
> > So now it turns out that the hobbit is another bipedal hominoid with an
> > abducted hallux: Oreopithecus, Ardipithecus, and now Homo floresiensis
> > which I believe will eventually be removed from Homo and will be given a
> > new generic designation:
> >
> > Journal of Human Evolution 57:538-554
> > Descriptions of the lower limb skeleton of Homo floresiensis
> > W.L. Jungers, S.G. Larson, W. Harcourt-Smith, M.J. Morwood, T. Sutikna,
> > Rokhus Due Awe, T. Djubiantono
> > Bones of the lower extremity have been recovered for up to nine
> > different individuals of Homo floresiensis – LB1, LB4, LB6, LB8,
> > LB9, LB10, LB11, LB13, and LB14. LB1 is represented by a bony pelvis
> > (damaged but now repaired), femora, tibiae, fibulae, patellae, and
> > numerous foot bones. LB4/2 is an immature right tibia lacking epiphyses.
> > LB6 includes a fragmentary metatarsal and two pedal phalanges. LB8 is a
> > nearly complete right tibia (shorter than that of LB1). LB9 is a
> > fragment of a hominin femoral diaphysis. LB10 is a proximal hallucal
> > phalanx. LB11 includes pelvic fragments and a fragmentary metatarsal.
> > LB13 is a patellar fragment, and LB14 is a fragment of an acetabulum.
> > All skeletal remains recovered from Liang Bua were extremely fragile,
> > and some were badly damaged when they were removed temporarily from
> > Jakarta. At present, virtually all fossil materials have been returned,
> > stabilized, and hardened. These skeletal remains are described and
> > illustrated photographically. The lower limb skeleton exhibits a
> > uniquely mosaic pattern, with many primitive-like morphologies; we have
> > been unable to find this combination of ancient and derived (more
> > human-like) features in either healthy or pathological modern humans,
> > regardless of body size. Bilateral asymmetries are slight in the
> > postcranium, and muscle markings are clearly delineated on all bones.
> > The long bones are robust, and the thickness of their cortices is well
> > within the ranges seen in healthy modern humans. LB1 is most probably a
> > female based on the shape of her greater sciatic notch, and the marked
> > degree of lateral iliac flaring recalls that seen in australopithecines
> > such as "Lucy" (AL 288-1). The metatarsus has a human-like
> > robusticity formula, but the proximal pedal phalanges are relatively
> > long and robust (and slightly curved). The hallux is fully adducted, but
> > we suspect that a medial longitudinal arch was absent.
>
Marcel, they say "adducted", not "abducted"!
--marc
> So now it turns out that the hobbit is another bipedal hominoid with an
> abducted hallux: Oreopithecus, Ardipithecus, and now Homo floresiensis
> which I believe will eventually be removed from Homo and will be given a
> new generic designation:
>
> Journal of Human Evolution 57:538-554
> Descriptions of the lower limb skeleton of Homo floresiensis
> W.L. Jungers, S.G. Larson, W. Harcourt-Smith, M.J. Morwood, T. Sutikna,
> Rokhus Due Awe, T. Djubiantono
> Bones of the lower extremity have been recovered for up to nine
> different individuals of Homo floresiensis – LB1, LB4, LB6, LB8,
> LB9, LB10, LB11, LB13, and LB14. LB1 is represented by a bony pelvis
> (damaged but now repaired), femora, tibiae, fibulae, patellae, and
> numerous foot bones. LB4/2 is an immature right tibia lacking epiphyses.
> LB6 includes a fragmentary metatarsal and two pedal phalanges. LB8 is a
> nearly complete right tibia (shorter than that of LB1). LB9 is a
> fragment of a hominin femoral diaphysis. LB10 is a proximal hallucal
> phalanx. LB11 includes pelvic fragments and a fragmentary metatarsal.
> LB13 is a patellar fragment, and LB14 is a fragment of an acetabulum.
> All skeletal remains recovered from Liang Bua were extremely fragile,
> and some were badly damaged when they were removed temporarily from
> Jakarta. At present, virtually all fossil materials have been returned,
> stabilized, and hardened. These skeletal remains are described and
> illustrated photographically. The lower limb skeleton exhibits a
> uniquely mosaic pattern, with many primitive-like morphologies; we have
> been unable to find this combination of ancient and derived (more
> human-like) features in either healthy or pathological modern humans,
> regardless of body size. Bilateral asymmetries are slight in the
> postcranium, and muscle markings are clearly delineated on all bones.
> The long bones are robust, and the thickness of their cortices is well
> within the ranges seen in healthy modern humans. LB1 is most probably a
> female based on the shape of her greater sciatic notch, and the marked
> degree of lateral iliac flaring recalls that seen in australopithecines
> such as "Lucy" (AL 288-1). The metatarsus has a human-like
> robusticity formula, but the proximal pedal phalanges are relatively
> long and robust (and slightly curved). The hallux is fully adducted, but
> we suspect that a medial longitudinal arch was absent.
Correction. "The hallux is fully adducted, but we suspect that a medial longitudinal arch was absent."
-Steve
--- In paleoanthropology@yahoogroups.com, "newpapyrus" <newpapyrus@...> wrote: > > So now it turns out that the hobbit is another bipedal hominoid with an > abducted hallux: Oreopithecus, Ardipithecus, and now Homo floresiensis > which I believe will eventually be removed from Homo and will be given a > new generic designation: > > Journal of Human Evolution > Volume 57, Issue 5, > Descriptions of the lower limb skeleton of Homo floresiensis > Pages 538-554 > W.L. Jungers, S.G. Larson, W. Harcourt-Smith, M.J. Morwood, T. Sutikna, > Rokhus Due Awe, T. Djubiantono > > Abstract > Bones of the lower extremity have been recovered for up to nine > different individuals of Homo floresiensis – LB1, LB4, LB6, LB8, > LB9, LB10, LB11, LB13, and LB14. LB1 is represented by a bony pelvis > (damaged but now repaired), femora, tibiae, fibulae, patellae, and > numerous foot bones. LB4/2 is an immature right tibia lacking epiphyses. > LB6 includes a fragmentary metatarsal and two pedal phalanges. LB8 is a > nearly complete right tibia (shorter than that of LB1). LB9 is a > fragment of a hominin femoral diaphysis. LB10 is a proximal hallucal > phalanx. LB11 includes pelvic fragments and a fragmentary metatarsal. > LB13 is a patellar fragment, and LB14 is a fragment of an acetabulum. > All skeletal remains recovered from Liang Bua were extremely fragile, > and some were badly damaged when they were removed temporarily from > Jakarta. At present, virtually all fossil materials have been returned, > stabilized, and hardened. These skeletal remains are described and > illustrated photographically. The lower limb skeleton exhibits a > uniquely mosaic pattern, with many primitive-like morphologies; we have > been unable to find this combination of ancient and derived (more > human-like) features in either healthy or pathological modern humans, > regardless of body size. Bilateral asymmetries are slight in the > postcranium, and muscle markings are clearly delineated on all bones. > The long bones are robust, and the thickness of their cortices is well > within the ranges seen in healthy modern humans. LB1 is most probably a > female based on the shape of her greater sciatic notch, and the marked > degree of lateral iliac flaring recalls that seen in australopithecines > such as "Lucy" (AL 288-1). The metatarsus has a human-like > robusticity formula, but the proximal pedal phalanges are relatively > long and robust (and slightly curved). The hallux is fully adducted, but > we suspect that a medial longitudinal arch was absent. >
So now it turns out that the hobbit is another bipedal hominoid with an abducted hallux: Oreopithecus, Ardipithecus, and now Homo floresiensis which I believe will eventually be removed from Homo and will be given a new generic designation:
Journal of Human Evolution Volume 57, Issue 5, Descriptions of the lower limb skeleton of Homo floresiensis Pages 538-554 W.L. Jungers, S.G. Larson, W. Harcourt-Smith, M.J. Morwood, T. Sutikna, Rokhus Due Awe, T. Djubiantono
Abstract Bones of the lower extremity have been recovered for up to nine different individuals of Homo floresiensis – LB1, LB4, LB6, LB8, LB9, LB10, LB11, LB13, and LB14. LB1 is represented by a bony pelvis (damaged but now repaired), femora, tibiae, fibulae, patellae, and numerous foot bones. LB4/2 is an immature right tibia lacking epiphyses. LB6 includes a fragmentary metatarsal and two pedal phalanges. LB8 is a nearly complete right tibia (shorter than that of LB1). LB9 is a fragment of a hominin femoral diaphysis. LB10 is a proximal hallucal phalanx. LB11 includes pelvic fragments and a fragmentary metatarsal. LB13 is a patellar fragment, and LB14 is a fragment of an acetabulum. All skeletal remains recovered from Liang Bua were extremely fragile, and some were badly damaged when they were removed temporarily from Jakarta. At present, virtually all fossil materials have been returned, stabilized, and hardened. These skeletal remains are described and illustrated photographically. The lower limb skeleton exhibits a uniquely mosaic pattern, with many primitive-like morphologies; we have been unable to find this combination of ancient and derived (more human-like) features in either healthy or pathological modern humans, regardless of body size. Bilateral asymmetries are slight in the postcranium, and muscle markings are clearly delineated on all bones. The long bones are robust, and the thickness of their cortices is well within the ranges seen in healthy modern humans. LB1 is most probably a female based on the shape of her greater sciatic notch, and the marked degree of lateral iliac flaring recalls that seen in australopithecines such as "Lucy" (AL 288-1). The metatarsus has a human-like robusticity formula, but the proximal pedal phalanges are relatively long and robust (and slightly curved). The hallux is fully adducted, but we suspect that a medial longitudinal arch was absent.
Well, I had just finished reading John's analysis if the highly statistical cladistic analysis and as my eyes were glazing, your bit of humor rescued me. I knew you were having a bit of fun and I am sure John did also.
I haven't seen any evidence for "hairy feet" on these "hobbits", either. Hardly surprising, since, at the moment, all we have is fossil bones of same. Unless there's something going on out there that neither you nor I know about.
Anne G
Without my going over the characters, at least one statement here is incorrect. If only the 'hobbit' character state is in the outgroup, this indeed is evidence for plesiomorphy, but it implies that some or all other ingroup species are synapomorphic for another state, which is thus informative.
On Milton's comment, I haven't seen evidence for hairy feet on the Flores people, as distinct from those that Tolkien described.
Those interested in phylogenetic evidence for hominid evolution may have seen the recent cladistic analysis of hobbit relationships in the Journal of Human Evolution in which it is argued that the hobbit is among the basal lineages of Homo. This may be correct, but the analysis is problematic. Of the 60 characters 17 are cladistically invalid because all the character states for the ingroup (hominids including hobbit) are in the outgroup. This means that shared derived similarity cannot be distinguished from primitive retention. A further 21 characters were uninformative (even if they are correctly documented) for the hobbit because the hobbit character state is either in the outgroup (most cases) and therefore does not represent a cladistic feature, or is missing for the hobbit, or autapomorphic for the hobbit.
One character appears to be incorrectly documented or and problematically compared (character 3).
This leaves only 17 characters (less than a third of the total) that have the appearance of conforming to cladistic requirements and informative for similarities between the hobbit and other hominids. But even here the comparison are marred by the lack of descriptive documentation (actual measurements and illustrations) as well as an outgroup being limited to the African apes.
So whether the remaining 17 have any validity remains to be seen. But at this point the description of 'cladistic' is somewhat misleading and the result far from providing any confidence about its phylogenetic placement.
May I add that there are two further troublesome features about claims for ancestral status of hobbits? The first is the uniquely (in my experience) circular construction of hobbit dwellings. The second is the elongated hairy feet which, though perhaps consonant with those of Australopithecus afarensis, are otherwise worryingly un-hominid in more developed species.
Richard
No virus found in this incoming message. Checked by AVG - www.avg.com Version: 8.5.425 / Virus Database: 270.14.62/2499 - Release Date: 11/12/09 14:33:00
I haven't seen any evidence for "hairy feet" on these "hobbits", either. Hardly surprising, since, at the moment, all we have is fossil bones of same. Unless there's something going on out there that neither you nor I know about.
Anne G
Without my going over the characters, at least one statement here is incorrect. If only the 'hobbit' character state is in the outgroup, this indeed is evidence for plesiomorphy, but it implies that some or all other ingroup species are synapomorphic for another state, which is thus informative.
On Milton's comment, I haven't seen evidence for hairy feet on the Flores people, as distinct from those that Tolkien described.
Those interested in phylogenetic evidence for hominid evolution may have seen the recent cladistic analysis of hobbit relationships in the Journal of Human Evolution in which it is argued that the hobbit is among the basal lineages of Homo. This may be correct, but the analysis is problematic. Of the 60 characters 17 are cladistically invalid because all the character states for the ingroup (hominids including hobbit) are in the outgroup. This means that shared derived similarity cannot be distinguished from primitive retention. A further 21 characters were uninformative (even if they are correctly documented) for the hobbit because the hobbit character state is either in the outgroup (most cases) and therefore does not represent a cladistic feature, or is missing for the hobbit, or autapomorphic for the hobbit.
One character appears to be incorrectly documented or and problematically compared (character 3).
This leaves only 17 characters (less than a third of the total) that have the appearance of conforming to cladistic requirements and informative for similarities between the hobbit and other hominids. But even here the comparison are marred by the lack of descriptive documentation (actual measurements and illustrations) as well as an outgroup being limited to the African apes.
So whether the remaining 17 have any validity remains to be seen. But at this point the description of 'cladistic' is somewhat misleading and the result far from providing any confidence about its phylogenetic placement.
May I add that there are two further troublesome features about claims for ancestral status of hobbits? The first is the uniquely (in my experience) circular construction of hobbit dwellings. The second is the elongated hairy feet which, though perhaps consonant with those of Australopithecus afarensis, are otherwise worryingly un-hominid in more developed species.
Richard
No virus found in this incoming message. Checked by AVG - www.avg.com Version: 8.5.425 / Virus Database: 270.14.62/2499 - Release Date: 11/12/09 14:33:00
But it was a nice attempt. Nevertheless one never knows what might turn up and so I had to take it seriously.
John Grehan
From: paleoanthropology@yahoogroups.com [mailto:paleoanthropology@yahoogroups.com] On Behalf Of Richard Milton Sent: Thursday, November 12, 2009 6:55 PM To: paleoanthropology@yahoogroups.com Subject: Re: [paleoanthropology] Re: hobbit phylogeny
Please forgive my attempts to enliven a dull Thursday with a little weak humour. I have now completely recovered my sense of seriousness.
I haven't seen any evidence for "hairy feet" on these "hobbits", either. Hardly surprising, since, at the moment, all we have is fossil bones of same. Unless there's something going on out there that neither you nor I know about.
Anne G
Without my going over the characters, at least one statement here is incorrect. If only the 'hobbit' character state is in the outgroup, this indeed is evidence for plesiomorphy, but it implies that some or all other ingroup species are synapomorphic for another state, which is thus informative.
On Milton's comment, I haven't seen evidence for hairy feet on the Flores people, as distinct from those that Tolkien described.
Those interested in phylogenetic evidence for hominid evolution may have seen the recent cladistic analysis of hobbit relationships in the Journal of Human Evolution in which it is argued that the hobbit is among the basal lineages of Homo. This may be correct, but the analysis is problematic. Of the 60 characters 17 are cladistically invalid because all the character states for the ingroup (hominids including hobbit) are in the outgroup. This means that shared derived similarity cannot be distinguished from primitive retention. A further 21 characters were uninformative (even if they are correctly documented) for the hobbit because the hobbit character state is either in the outgroup (most cases) and therefore does not represent a cladistic feature, or is missing for the hobbit, or autapomorphic for the hobbit.
One character appears to be incorrectly documented or and problematically compared (character 3).
This leaves only 17 characters (less than a third of the total) that have the appearance of conforming to cladistic requirements and informative for similarities between the hobbit and other hominids. But even here the comparison are marred by the lack of descriptive documentation (actual measurements and illustrations) as well as an outgroup being limited to the African apes.
So whether the remaining 17 have any validity remains to be seen. But at this point the description of 'cladistic' is somewhat misleading and the result far from providing any confidence about its phylogenetic placement.
May I add that there are two further troublesome features about claims for ancestral status of hobbits? The first is the uniquely (in my experience) circular construction of hobbit dwellings. The second is the elongated hairy feet which, though perhaps consonant with those of Australopithecus afarensis, are otherwise worryingly un-hominid in more developed species.
I haven't seen any evidence for "hairy feet" on these "hobbits", either. Hardly surprising, since, at the moment, all we have is fossil bones of same. Unless there's something going on out there that neither you nor I know about.
Anne G
Without my going over the characters, at least one statement here is incorrect. If only the 'hobbit' character state is in the outgroup, this indeed is evidence for plesiomorphy, but it implies that some or all other ingroup species are synapomorphic for another state, which is thus informative.
On Milton's comment, I haven't seen evidence for hairy feet on the Flores people, as distinct from those that Tolkien described.
Those interested in phylogenetic evidence for hominid evolution may have seen the recent cladistic analysis of hobbit relationships in the Journal of Human Evolution in which it is argued that the hobbit is among the basal lineages of Homo. This may be correct, but the analysis is problematic. Of the 60 characters 17 are cladistically invalid because all the character states for the ingroup (hominids including hobbit) are in the outgroup. This means that shared derived similarity cannot be distinguished from primitive retention. A further 21 characters were uninformative (even if they are correctly documented) for the hobbit because the hobbit character state is either in the outgroup (most cases) and therefore does not represent a cladistic feature, or is missing for the hobbit, or autapomorphic for the hobbit.
One character appears to be incorrectly documented or and problematically compared (character 3).
This leaves only 17 characters (less than a third of the total) that have the appearance of conforming to cladistic requirements and informative for similarities between the hobbit and other hominids. But even here the comparison are marred by the lack of descriptive documentation (actual measurements and illustrations) as well as an outgroup being limited to the African apes.
So whether the remaining 17 have any validity remains to be seen. But at this point the description of 'cladistic' is somewhat misleading and the result far from providing any confidence about its phylogenetic placement.
May I add that there are two further troublesome features about claims for ancestral status of hobbits? The first is the uniquely (in my experience) circular construction of hobbit dwellings. The second is the elongated hairy feet which, though perhaps consonant with those of Australopithecus afarensis, are otherwise worryingly un-hominid in more developed species.
I haven't seen any evidence for "hairy feet" on these "hobbits", either. Hardly surprising, since, at the moment, all we have is fossil bones of same. Unless there's something going on out there that neither you nor I know about.
Anne G
Without my going over the characters, at least one statement here is incorrect. If only the 'hobbit' character state is in the outgroup, this indeed is evidence for plesiomorphy, but it implies that some or all other ingroup species are synapomorphic for another state, which is thus informative.
On Milton's comment, I haven't seen evidence for hairy feet on the Flores people, as distinct from those that Tolkien described.
Those interested in phylogenetic evidence for hominid evolution may have seen the recent cladistic analysis of hobbit relationships in the Journal of Human Evolution in which it is argued that the hobbit is among the basal lineages of Homo. This may be correct, but the analysis is problematic. Of the 60 characters 17 are cladistically invalid because all the character states for the ingroup (hominids including hobbit) are in the outgroup. This means that shared derived similarity cannot be distinguished from primitive retention. A further 21 characters were uninformative (even if they are correctly documented) for the hobbit because the hobbit character state is either in the outgroup (most cases) and therefore does not represent a cladistic feature, or is missing for the hobbit, or autapomorphic for the hobbit.
One character appears to be incorrectly documented or and problematically compared (character 3).
This leaves only 17 characters (less than a third of the total) that have the appearance of conforming to cladistic requirements and informative for similarities between the hobbit and other hominids. But even here the comparison are marred by the lack of descriptive documentation (actual measurements and illustrations) as well as an outgroup being limited to the African apes.
So whether the remaining 17 have any validity remains to be seen. But at this point the description of 'cladistic' is somewhat misleading and the result far from providing any confidence about its phylogenetic placement.
May I add that there are two further troublesome features about claims for ancestral status of hobbits? The first is the uniquely (in my experience) circular construction of hobbit dwellings. The second is the elongated hairy feet which, though perhaps consonant with those of Australopithecus afarensis, are otherwise worryingly un-hominid in more developed species.
Good point and I appreciate that feedback.
That they are cladistically correct for the other taxa I would agree, but you
are right that the plesiomorphic state is informative in excluding the hobbit
from those other taxa as defined by those apomorphies. I’ll take another
look at those clusterings.
John Grehan
From: paleoanthropology@yahoogroups.com
[mailto:paleoanthropology@yahoogroups.com] On
Behalf Of leigh van valen Sent: Thursday, November 12, 2009
12:13 PM To:
paleoanthropology@yahoogroups.com Subject: [paleoanthropology] Re:
hobbit phylogeny
Without
my going over the characters, at least one statement here is incorrect. If
only the 'hobbit' character state is in the outgroup, this indeed is evidence
for plesiomorphy, but it implies that some or all other ingroup species are
synapomorphic for another state, which is thus informative.
On Milton's comment, I haven't seen evidence for
hairy feet on the Flores people, as distinct
from those that Tolkien described.
Those
interested in phylogenetic evidence for hominid evolution may have
seen the recent cladistic analysis of hobbit relationships in the
Journal of Human Evolution in which it is argued that the hobbit is
among the basal lineages of Homo. This may be correct, but the analysis
is problematic. Of the 60 characters 17 are cladistically invalid
because all the character states for the ingroup (hominids including
hobbit) are in the outgroup. This means that shared derived similarity
cannot be distinguished from primitive retention. A further 21
characters were uninformative (even if they are correctly documented)
for the hobbit because the hobbit character state is either in the
outgroup (most cases) and therefore does not represent a cladistic
feature, or is missing for the hobbit, or autapomorphic for the hobbit.
One character appears to be incorrectly documented or and
problematically compared (character 3).
This leaves only 17 characters (less than a third of the total) that
have the appearance of conforming to cladistic requirements and
informative for similarities between the hobbit and other hominids. But
even here the comparison are marred by the lack of descriptive
documentation (actual measurements and illustrations) as well as an
outgroup being limited to the African apes.
So whether the remaining 17 have any validity remains to be seen. But
at this point the description of 'cladistic' is somewhat misleading and
the result far from providing any confidence about its phylogenetic
placement.
May I
add that there are two further troublesome features about claims for ancestral
status of hobbits? The first is the uniquely (in my experience) circular
construction of hobbit dwellings. The second is the elongated hairy feet which,
though perhaps consonant with those of Australopithecus afarensis, are
otherwise worryingly un-hominid in more developed species.
Without my going over the characters, at least one statement here
is incorrect. If only the 'hobbit' character state is in the outgroup,
this indeed is evidence for plesiomorphy, but it implies that some or
all other ingroup species are synapomorphic for another state, which is
thus informative.
On Milton's comment, I haven't seen evidence for hairy feet on the
Flores people, as distinct from those that Tolkien described.
Those interested in phylogenetic evidence for hominid evolution may have
seen the recent cladistic analysis of hobbit relationships in the
Journal of Human Evolution in which it is argued that the hobbit is
among the basal lineages of Homo. This may be correct, but the analysis
is problematic. Of the 60 characters 17 are cladistically invalid
because all the character states for the ingroup (hominids including
hobbit) are in the outgroup. This means that shared derived similarity
cannot be distinguished from primitive retention. A further 21
characters were uninformative (even if they are correctly documented)
for the hobbit because the hobbit character state is either in the
outgroup (most cases) and therefore does not represent a cladistic
feature, or is missing for the hobbit, or autapomorphic for the hobbit.
One character appears to be incorrectly documented or and
problematically compared (character 3).
This leaves only 17 characters (less than a third of the total) that
have the appearance of conforming to cladistic requirements and
informative for similarities between the hobbit and other hominids. But
even here the comparison are marred by the lack of descriptive
documentation (actual measurements and illustrations) as well as an
outgroup being limited to the African apes.
So whether the remaining 17 have any validity remains to be seen. But
at this point the description of 'cladistic' is somewhat misleading and
the result far from providing any confidence about its phylogenetic
placement.
May
I add that there are two further troublesome features about claims for
ancestral status of hobbits? The first is the uniquely (in my
experience) circular construction of hobbit dwellings. The second is
the elongated hairy feet which, though perhaps consonant with those of
Australopithecus afarensis, are otherwise worryingly un-hominid in more
developed species.
Good point about the feet. I intend to go
back to the feet descriptions and see what they show in detail with respect to ‘Homo”
(I have yet to identify and confirm what defines this genus with respect to the
taxa purported to be members). I don’t recall that the feet were hairy -
?? Housing – I have not seen that. May be interesting.
As an aside, some of you already know, but
the Hobbit lacks frontal sinuses. Not necessarily phylogenetically significant
as bonobos also usually lack the frontal sinuses whereas chimps have them (as
do humans – but don’t jump to conclusions about that). The longitudinal
section of the hobbit skull seems to show a posteriorly thick upper palate
which conforms to hominids and orangutans, but not African apes, but the
quality is too poor to show whether the thickness actually increases
posteriorly – an australopith and orangutan trait.
John Grehan
From:
paleoanthropology@yahoogroups.com [mailto:paleoanthropology@yahoogroups.com] On Behalf Of Richard Milton Sent: Thursday, November 12, 2009
7:48 AM To:
paleoanthropology@yahoogroups.com Subject: Re: [paleoanthropology]
hobbit phylogeny
May I add that there are two further troublesome features
about claims for ancestral status of hobbits? The first is the uniquely (in my
experience) circular construction of hobbit dwellings. The second is the
elongated hairy feet which, though perhaps consonant with those of
Australopithecus afarensis, are otherwise worryingly un-hominid in more
developed species.
Those
interested in phylogenetic evidence for hominid evolution may have seen the
recent cladistic analysis of hobbit relationships in the Journal of Human
Evolution in which it is argued that the hobbit is among the basal lineages of
Homo. This may be correct, but the analysis is problematic. Of the 60
characters 17 are cladistically invalid because all the character states for
the ingroup (hominids including hobbit) are in the outgroup. This means that
shared derived similarity cannot be distinguished from primitive retention. A further
21 characters were uninformative (even if they are correctly documented) for
the hobbit because the hobbit character state is either in the outgroup (most
cases) and therefore does not represent a cladistic feature, or is missing for
the hobbit, or autapomorphic for the hobbit.
One
character appears to be incorrectly documented or and problematically compared
(character 3).
This
leaves only 17 characters (less than a third of the total) that have the
appearance of conforming to cladistic requirements and informative for
similarities between the hobbit and other hominids. But even here the
comparison are marred by the lack of descriptive documentation (actual
measurements and illustrations) as well as an outgroup being limited to the
African apes.
So
whether the remaining 17 have any validity remains to be seen. But at this
point the description of ‘cladistic’ is somewhat misleading and the
result far from providing any confidence about its phylogenetic placement.
May I add that there are two further troublesome features about claims for ancestral status of hobbits? The first is the uniquely (in my experience) circular construction of hobbit dwellings. The second is the elongated hairy feet which, though perhaps consonant with those of Australopithecus afarensis, are otherwise worryingly un-hominid in more developed species.
Those interested in phylogenetic evidence for hominid evolution may have seen the recent cladistic analysis of hobbit relationships in the Journal of Human Evolution in which it is argued that the hobbit is among the basal lineages of Homo. This may be correct, but the analysis is problematic. Of the 60 characters 17 are cladistically invalid because all the character states for the ingroup (hominids including hobbit) are in the outgroup. This means that shared derived similarity cannot be distinguished from primitive retention. A further 21 characters were uninformative (even if they are correctly documented) for the hobbit because the hobbit character state is either in the outgroup (most cases) and therefore does not represent a cladistic feature, or is missing for the hobbit, or autapomorphic for the hobbit.
One character appears to be incorrectly documented or and problematically compared (character 3).
This leaves only 17 characters (less than a third of the total) that have the appearance of conforming to cladistic requirements and informative for similarities between the hobbit and other hominids. But even here the comparison are marred by the lack of descriptive documentation (actual measurements and illustrations) as well as an outgroup being limited to the African apes.
So whether the remaining 17 have any validity remains to be seen. But at this point the description of ‘cladistic’ is somewhat misleading and the result far from providing any confidence about its phylogenetic placement.
Those interested in phylogenetic evidence for hominid
evolution may have seen the recent cladistic analysis of hobbit relationships
in the Journal of Human Evolution in which it is argued that the hobbit is
among the basal lineages of Homo. This may be correct, but the analysis is
problematic. Of the 60 characters 17 are cladistically invalid because all the
character states for the ingroup (hominids including hobbit) are in the
outgroup. This means that shared derived similarity cannot be distinguished
from primitive retention. A further 21 characters were uninformative (even if
they are correctly documented) for the hobbit because the hobbit character
state is either in the outgroup (most cases) and therefore does not represent a
cladistic feature, or is missing for the hobbit, or autapomorphic for the
hobbit.
One character appears to be incorrectly documented or and
problematically compared (character 3).
This leaves only 17 characters (less than a third of the
total) that have the appearance of conforming to cladistic requirements and
informative for similarities between the hobbit and other hominids. But even
here the comparison are marred by the lack of descriptive documentation (actual
measurements and illustrations) as well as an outgroup being limited to the
African apes.
So whether the remaining 17 have any validity remains
to be seen. But at this point the description of ‘cladistic’ is
somewhat misleading and the result far from providing any confidence about its
phylogenetic placement.
High mitogenomic evolutionary rates and time dependency
Sankar Subramanian1, 2, Dee R. Denver3, 4, Craig D. Millar2, Tim Heupink1, Angelique Aschrafi3, 5, Steven D. Emslie6, Carlo Baroni7 and David M. Lambert1, 3,
CORVALLIS,Ore. - Penguins that died 44,000 years ago in Antarctica have providedextraordinary frozen DNA samples that challenge the accuracy oftraditional genetic aging measurements, and suggest those approacheshave been routinely underestimating the age of many specimens by 200 to600 percent.
Inother words, a biological specimen determined by traditional DNAtesting to be 100,000 years old may actually be 200,000 to 600,000years old, researchers suggest in a new report in Trends in Genetics, a professional journal.
The findings raise doubts about the accuracy of many evolutionary rates based on conventional types of genetic analysis.
"Someearlier work based on small amounts of DNA indicated this same problem,but now we have more conclusive evidence based on the study of almostan entire mitochondrial genome," said Dee Denver, an evolutionarybiologist with the Center for Genome Research and Biocomputing atOregon State University.
"Theobservations in this report appear to be fundamental and should extendto most animal species," he added. "We believe that traditional DNAdating techniques are fundamentally flawed, and that the rates ofevolution are in fact much faster than conventional technologies haveled us to believe."
Thefindings, researchers say, are primarily a challenge to the techniquesused to determine the age of a sample by genetic analysis alone, ratherthan by other observations about fossils. In particular, they may forcea widespread re-examination of determinations about when one speciessplit off from another, if that determination was based largely ongenetic evidence.
Foryears, researchers have been using their understanding of the rates ofgenetic mutations in cells to help date ancient biological samples, andin what's called "phylogenetic comparison," used that information alongwith fossil evidence to determine the dates of fossils and the historyof evolution. The rates of molecular evolution "underpin much of modernevolutionary biology," the researchers noted in their report.
"Forthe genetic analysis to be accurate, however, you must have the rightmolecular clock rate," Denver said. "We now think that many geneticchanges were happening that conventional DNA analysis did not capture.They were fairly easy to use and apply but also too indirect, andinaccurate as a result."
Thisconclusion, researchers said, was forced by the study of many penguinbones that were well preserved by sub-freezing temperatures inAntarctica. These penguins live in massive rookeries, have inhabitedthe same areas for thousands of years, and it was comparatively simpleto identify bones of different ages just by digging deeper in areaswhere they died and their bones piled up.
Fortheir study, the scientists used a range of mitochondrial DNA found inbones ranging from 250 years to about 44,000 years old.
"Ina temperate zone when an animal dies and falls to the ground, their DNAmight degrade within a year," Denver said. "In Antarctica the sameremains are well-preserved for tens of thousands of years. It's aremarkable scientific resource."
Aprecise study of this ancient DNA was compared to the known ages of thebones, and produced results that were far different than conventionalanalysis would have suggested. Researchers also determined thatdifferent types of DNA sequences changed at different rates.
Asidefrom raising doubts about the accuracy of many specimens dated withconventional approaches, the study may give researchers tools toimprove their future dating estimates, Denver said.
###
Collaboratorson the research included scientists from OSU, Griffith University inAustralia, the University of Auckland in New Zealand, Massey Universityin New Zealand, University of North Carolina in Wilmington, the ScrippsResearch Institute, and Universita' di Pisa in Italy.
The studies were supported by the National Science Foundation, National Geographic Society, and other agencies.
Jeez. When did they ever include Piltdown in a textbook, anywhere(of course, you have to remember that when I lived in Texas, I never laid eyes on that kind of textbook)? I never recall seeing any mention of Piltdown except in some "popular" books on human evolution, and by the time I saw this, it was known that Piltdown was a hoax.
Anne G
First, on Piltdown, it is a paradox that what goes into textbooks is often decided by school boards made up of generally uneducated ding bats. I think the inclusion of Piltdown is a deliberate creationists strategy. It demonstrates the "flaws" of evolution. On the Apiths, they post date the chimp-hominid split and I cannot see going from knuckle walking to erect and back to knuckle walking. Orrorin, predating Apiths, might have been the first of the hominids off of the assembly line of the chimp-human ancestor but Orrorins femur is more like mine than Apiths. That's curious. Maybe Apiths are a side line and we are still looking for Orrorins descendents. If I was younger I would pick up a pick and trowel and head for Africa.
Jack
-------------------------------------------------- From: "jim" <canovan@twmi.rr.com> Sent: Tuesday, November 10, 2009 11:01 AM To: <paleoanthropology@yahoogroups.com> Subject: [paleoanthropology] Re: New Ardipithecus finds ...
> > Hi Jack, > > GOOD ONE!! Very nice column! Can't say I buy your 'Flores' clip but I > just loved it when you noted that all future finds must carry the banner, > "THIS one will CHANGE all we know about MAN's evolution" ...Ha HAHHH! You > NAILED it, my friend!! > (:)) > best, > ~Jim > > PS- > And PILTDOWN.....WHY on earth, after ALL these years, must PILTDOWN still > be shown with other skulls??!! What POSSIBLE good can that do?! > PPS - > You got me going in the RANDOM THOUGHT DEPARTMENT NOW: > I'm beginning to wonder if - as many as half our Australopith remains > might not represent CHIMP ancestry?? > > > > > > > > --- In paleoanthropology@yahoogroups.com, "Jack Kilmon" <jkilmon@...> > wrote: >> >> Hiya, Jim, Anne ole buddy: >> >> I can't help but think about what has happened in paleoanthropology since >> I >> first became interested in human evolution. My first text book had >> Piltdown >> Man in it with a reconstruction that, because he was "English," was much >> more sophisticated than a stooped over, hairy Neanderthal and >> Pithecanthropus and Sinanthropus (The Chinese had to have their own also) >> and Raymond Dart's infant skull of Australopithecus africanus. I wonder >> where that old textbook is? Then along came the Leakeys and human >> evolution >> was concentrated almost solely on Africa and Olduvai gorge was the "womb" >> of >> human evolution. We had Zinjanthropus/Paranthropus/Australopithecus, >> Kenyanthropus and Orrorin. A whole gaggle of Australopithecines began to >> appear, garhi, aethiopicus, anamensis and I began to see different Homos >> like habilis, rudolfensis, ergaster and heidelbergensis. When "Lucy" was >> found, I think it had fossil hunters looking in new places and recently >> Ardipithecus, Sahelanthropus competed in the search for the LCA of us and >> chimps. Now we have those enigmatic little people of Flores. The >> "family >> trees" of hominids were always somewhat simple. A mysterious ancestor >> splitting off chimps on one side and hominids on the other and there was >> Apiths and Homo but the hominid side is starting to look more like a >> mangrove tree with roots entangled and multiple branches. Now every time >> we >> find a new fossil you can bet money the article will say "rewriting human >> evolution." It has been an interesting ride over the last half century >> and >> its just going to get more interesting because we probably have not seen >> a >> tenth of the genera and species of hominids. Flores is probably a new >> Genus. >> >> Jack >> >> >> >> -------------------------------------------------- >> From: "jim" <canovan@...> >> Sent: Tuesday, October 06, 2009 9:03 AM >> To: <paleoanthropology@yahoogroups.com> >> Subject: [paleoanthropology] Re: New Ardipithecus finds ... >> >> > >> > Anne, >> > Yes, they feel Ar. ramidus WAS bipedal and I do hope their conclusions >> > to >> > be correct. Perhaps future dicoveries will lend better evidence. I >> > don't >> > think there can be any doubt Ardi was VERY close to the later >> > australopiths. >> > >> > Torfinn, >> > OK. Your points ARE well taken. I don't wish to drag this thing on. I >> > will >> > only say that I've recently conferred with Milford Wolpoff on this >> > 'hominid biped requirement' and he concurs my viewpoint. >> > So, now that I might retain a modicum of dignity, please let me >> > continue >> > to hope I'm not alone in this stubborn & tenacious stance. >> > (:)) >> > best, >> > ~jim >> > >> > >> > >> > >> > >> > --- In paleoanthropology@yahoogroups.com, Anne Gilbert <avgilbert@> >> > wrote: >> >> >> >> Jim: >> >> >> >> Yes, the opposable feet are kind of apish-looking, to me, at least. >> >> OTOH, all I can say is, that according to White et al, Ar. ramidus >> >> walked, after a fashion, upright, on two feet, and they claim the >> >> pelvis >> >> is more like that of australopithecines, who apparently always walked >> >> upright. I'm not making any claims myself, though. >> >> Anne G >> >> >> >> >> >> >> >> Anne, >> >> No problem. I had no idea that was a typo; thought it was, like, >> >> initials of something or other. >> >> As for my questioning of hominid I.D. for Ardi, I don't mean to >> >> imply >> >> that I regard this genus as quad. I'm simply wondering about status >> >> because of vague dates(before or after Pan/Homo split?) and the foot >> >> morphology which plainly calls for simian locomotion. My actual hope >> >> is >> >> Ardi is BIPED(hence my questioning of the fully opposable big toe >> >> reconstruction). >> >> >> >> . >> >> >> > >> > >> > >> > >> > ------------------------------------ >> > >> > Yahoo! Groups Links >> > >> > >> > >> > >> >> >> >> > >> > No virus found in this incoming message. >> > Checked by AVG - www.avg.com >> > Version: 8.5.420 / Virus Database: 270.14.4/2417 - Release Date: >> > 10/06/09 >> > 06:50:00 >> > >> > > > > > ------------------------------------ > > Yahoo! Groups Links > > > >
> > No virus found in this incoming message. > Checked by AVG - www.avg.com > Version: 8.5.425 / Virus Database: 270.14.59/2494 - Release Date: 11/10/09 > 07:38:00 >