Discussion:
Miocene Hominoidea
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Primum Sapienti
2024-02-10 06:26:23 UTC
Permalink
State of the art of a neverending controversy
A Urciuoli & DM Alba 2023 JHE 175,103309
doi 10.1016/j.jhevol.2022.103309
The link and the REAL abstract

https://www.sciencedirect.com/science/article/pii/S0047248422001695

Abstract
Hominoids diverged from cercopithecoids during
the Oligocene in Afro-Arabia, initially
radiating in that continent and subsequently
dispersing into Eurasia. From the Late Miocene
onward, the geographic range of hominoids
progressively shrank, except for hominins,
which dispersed out of Africa during the
Pleistocene. Although the overall picture of
hominoid evolution is clear based on available
fossil evidence, many uncertainties persist
regarding the phylogeny and paleobiogeography
of Miocene apes (nonhominin hominoids), owing
to their sparse record, pervasive homoplasy,
and the decimated current diversity of this
group. We review Miocene ape systematics and
evolution by focusing on the most parsimonious
cladograms published during the last decade.
First, we provide a historical account of the
progress made in Miocene ape phylogeny and
paleobiogeography, report an updated
classification of Miocene apes, and provide a
list of Miocene ape species-locality
occurrences together with an analysis of their
paleobiodiversity dynamics. Second, we discuss
various critical issues of Miocene ape
phylogeny and paleobiogeography (hylobatid and
crown hominid origins, plus the relationships
of Oreopithecus) in the light of the highly
divergent results obtained from cladistic
analyses of craniodental and postcranial
characters separately. We conclude that
cladistic efforts to disentangle Miocene ape
phylogeny are potentially biased by a
long-branch attraction problem caused by the
numerous postcranial similarities shared
between hylobatids and hominids—despite the
increasingly held view that they are likely
homoplastic to a large extent, as illustrated
by Sivapithecus and Pierolapithecus—and
further aggravated by abundant missing data
owing to incomplete preservation. Finally, we
argue that—besides the recovery of additional
fossils, the retrieval of paleoproteomic data,
and a better integration between cladistics
and geometric morphometrics—Miocene ape
phylogenetics should take advantage of
total-evidence (tip-dating) Bayesian methods
of phylogenetic inference combining
morphologic, molecular, and
chronostratigraphic data. This would hopefully
help ascertain whether hylobatid divergence
was more basal than currently supported.

"Despite the progress made during the last
decades in terms of Miocene ape systematics,
many phylogenetic and paleobiogeographic
uncertainties persist."

"Too many Miocene ape genera are still known
mainly from fragmentary dentognathic remains..."

"Miocene apes are much more diverse than their
extant counterparts, evincing a suite of mosaic
morphologies that are essential to reconstruct
the evolutionary history of the Hominoidea. Here
we review Miocene ape evolution with emphasis on
their phylogenetic relationships and the
paleobiogeographic scenarios that derive from
them. The oldest hominoids from the Oligocene,
Miocene catarrhines of uncertain affinities, and
Late Miocene purported hominins are excluded from
this review."
Marc Verhaegen
2024-02-10 11:55:34 UTC
Permalink
Systematics of Miocene apes:
State of the art of a neverending controversy
A Urciuoli & DM Alba 2023 JHE 175,103309
doi 10.1016/j.jhevol.2022.103309
https://www.sciencedirect.com/science/article/pii/S0047248422001695

There is no serious controversy anymore AFAICS:
Mario Vaneechoutte cs 2024 Nature Anthropology 2,10007
“Have we been barking up the wrong ancestral tree?
Australopithecines are probably not our ancestors”
open access https://www.sciepublish.com/article/pii/94

Hominoids diverged from cercopithecoids during the Oligocene in Afro-Arabia,
they colonized the coastal forests of the island archipels between Afro-Arabia & Eurasia:
they became "aquarboreal" (google), where they waded bipedally + climbed arms overhead:
this explains why early apes began differing from "monkeys":
larger size, vertical & centrally-placed spine (upright), +-shortened lumbar spine, much wider pelvis & thorax + broad sternum (Hominoidea = Latisternalia) -> dorsally-placed scapulas + very long arms.
First, hylobatids (lesser apes, today gibbons, siamangs...) followed the S.Asian coasts.
When Arabia reached Eurasia (Mesopotamian Seaway Closure 15 Ma), this split pongids-sivapiths East (S.Asian coastal forests) & hominids-dryopiths West (Medit.coastal forests + incipient Red Sea) + inland along rivers, e.g. Oreopithecus "swamp ape", Trachilos BP footprints etc.
Late-Miocene Hominids died out, except in the Red Sea:
Gorilla 8-7 Ma followed the incipient northern Rift -> Afar: Lucy etc. Praeanthropus afarensis->boisei etc.
When the Red Sea opened into the Gulf of Aden 6-5 Ma (possibly exactly 5.33 Ma, caused by the Zanclean mega-flood),
a) Pan turned right along the E.Afr.coast -> incipient southern Rift -> transvaal: Taung etc. Australopithecus africanus->robustus
(parallel evolution late-Pliocene "gracile" afarensis//africanus -> early-Pleist."robust" boisei//robustus in E resp. S.Africa):
Pan & Gorilla evolved (later Pleist.?) knuckle-walking in parallel, e.g.
1994 Hum.Evol.9:121-139 "Australopithecines: ancestors of the African apes?"
1996 Hum.Evol.11:35-41"Morphological distance between australopithecine, human and ape skulls"
b) Homo turned left along the S.Asian coasts, explaining
-- early-Pleistocene Homo in Java, fossilised amid barnacles-shellfish etc., later Flores, Peking etc.
-- the absence of Pliocene African RV DNA in humans:
1) "Evolution of type C viral genes: evidence for an Asian origin of man" RE Benveniste & GJ Todaro 1976 Nature 261:101-8: OWMs & apes incl. man possess, as a normal component of their cellular DNA, virogenes related to the RNA of a vims isolated from baboons (this) distinguishes those OWMs & apes that have evolved in Africa from those that have evolved in Asia. Among the apes, only gorilla & chimp seem by these criteria to be African - gibbon, orang & man are identified as Asian: most of man's evolution has occurred outside Africa.
2) "Lineage-specific expansions of retroviral insertions within the genomes of African great apes but not humans and orangutans" CT Yohn cs 2005 doi 10.1371/journal.pbio.0030110 ... Pan troglodytes endogenous retrovirus-1 (PTERV1) has become integrated in the germ-line of Afr.gr.ape & OWM spp, but is absent from human & Asian ape genomes ... a RV infection bombarded chimp & gorilla genomes independently & concurrently, 3-4 Ma ...
3) "Have we been barking up the wrong ancestral tree? Australopithecines are probably not our ancestors" Mario Vaneechoutte cs 2024 Nature Anthropol.2(1), 10007 open access doi org/10.35534/natanthropol.2023.10007: ... upright posture/gait is already present to different degrees even in Miocene apes : hominoid orthogrady is a primitive characteristic : knuckle-walking has evolved in parallel, independently in both Pan & Gorilla ... numerous similarities between australopithecines & extant African apes ... not our direct ancestors ... Apparently, Pleistocene Homo typically dispersed intercontinentally along coasts->rivers, starting from Indian Ocean coasts.

Recent insights in ape+human evolution:
Miocene Hominoidea were already aquarboreal in swamp/coastal forests (aqua=water, arbor=tree), google e.g.
- "aquarboreal"
- https://www.gondwanatalks.com/l/the-waterside-hypothesis-wading-led-to-upright-walking-in-early-humans/
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