A possible Chinese ancestor for Denisovans, Neanderthals and modern humans

Assigning human fossils older than around 250 ka to different groups of the genus Homo depends entirely on their physical features. That is because ancient DNA has yet to be found and analysed from specimens older than that. The phylogeny of older human remains is also generally restricted to the bones that make up their heads; 21 that are fixed together in the skull and face, plus the moveable lower jaw or mandible. Far more teeth than crania have been discovered and considerable weight is given to differences in human dentition. Teeth are not bones, but they are much more durable, having no fibrous structure and vary a great deal. The main problem for palaeoanthropologists is that living humans are very diverse in their cranial characteristics, and so it is reasonable to infer that all ancient human groups were characterised by such polymorphism, and may have overlapped in their physical appearance. A measure of this is that assigning fossils to anatomically modern humans, i.e. Homo sapiens, relies to a large extent on whether or not their lower mandible juts out to define a chin. All earlier hominins and indeed all other living apes might be regarded as ‘chinless wonders’! This pejorative term suggests dim-wittedness to most people, and anthropologists have had to inure themselves to such crude cultural conjecture.

The extraction, sequencing and comparison of ancient DNA from human fossils since 2010 has revealed that three distinct human species coexisted and interbred in Eurasia. Several well preserved examples of ancient Neanderthals and anatomically modern humans (AMH) have had their DNA sequenced, but a Denisovan genome has only emerged from a few bone fragments from the Denisova Cave in western Siberia. Whereas Neanderthals have well-known robust physical characters, until 2025 palaeoanthropologists had little idea of what Denisovans may have looked like. Then proteins and, most importantly, mitochondrial DNA (mtDNA) were extracted from a very robust skull found around 1931 in Harbin, China, dated at 146 ka. Analysis of the mtDNA and proteins, from dental plaque and bone respectively, reveal that the Harbin skull is likely to be that of a Denisovan. Previously it had been referred to as Homo longi, or ‘Dragon Man’, along with several other very robust Chinese skulls of a variety of ages.

The distorted Yunxian cranium (right) and its reconstruction (middle) [Credit: Guanghui Zhao] compared with the Harbin Denisovan cranium (left) [Hebei Geo University]

The sparse genetic data have been used to suggest the times when the three different coexisting groups diverged. DNA in Y chromosomes from Denisovans and Neanderthals suggest that the two lineages split from a common ancestor around 700 ka ago, whereas Neanderthals and modern humans diverged genetically at about 370 ka. Yet the presence of sections of DNA from both archaic groups in living humans and the discovery that a female Neanderthal from Denisova cave had a Neanderthal mother and a Denisovan father reveals that all three were interfertile when they met and interacted. Such admixture events clearly have implications for earlier humans. There are signs of at least 6 coexisting groups as far back as the Middle Pleistocene (781 to 126 ka), referred to by some as the ‘muddle in the middle’ because such an association has increasingly mystified palaeoanthropologists. A million-year-old, cranium found near Yunxian in Hubei Province, China, distorted by the pressure of sediments in which it was buried, has been digitally reconstructed.

This reconstruction encouraged a team of Chinese scientists, together with Chris Stringer of the UK Museum of Natural History, to undertake a complex statistical study of the Yunxian cranium. Their method compares it with anatomical data for all members of the genus Homo from Eurasia and Africa, i.e. as far back as the 2.4 Ma old H. habilis (Xiabo Feng and 12 others 2025. The phylogenetic position of the Yunxian cranium elucidates the origin of Homo longi and the Denisovans. Science, v. 389, p. 1320-1324; DOI: 10.1126/science.ado9202). The study has produced a plausible framework that suggests that the five large-brained humans known from 800 ka ago – Homo erectus (Asian), H. heidelbergensis, H. longi (Denisovans), H. sapiens, and H. neanderthalensis – began diverging from one another more than a million years ago. The authors regard the Yuxian specimen as an early participant in that evolutionary process. The fact that at least some remained interfertile long after the divergence began suggests that it was part of the earlier human evolutionary process. It is also possible that the repeated morphological divergence may stem from genetic drift. That process involves small populations with limited genetic diversity that are separated from other groups, perhaps by near-extinction in a population bottleneck or as a result of the founder effect when a small group splits from a larger population during migration. The global population of early humans was inevitably very low, and migrations would dilute and fragment each group’s gene pool.

The earliest evidence for migration of humans out of Africa emerged from the discovery of five 1.8 Ma old crania of H. erectus at Dmanisi to the east of the Black Sea in Georgia. similar archaic crania have been found in eastern Eurasia, especially China, at various localities with Early- to Middle Pleistocene dates. The earliest European large-brained humans – 1.2 to 0.8 Ma old H. antecessor from northern Spain – must have migrated a huge distance from either Africa or from eastern Eurasia and may have been a product of the divergence-convergence evolutionary framework suggested by Xiabo Feng and colleagues. Such a framework implies that even earlier members of what became the longi, heidelbergensis, neanderthalensis, and sapiens lineages may await either recognition or discovery elsewhere. But the whole issue raises questions about the widely held view that Homo sapiens first appeared 300 ka ago in North Africa and then populated the rest of that continent. Was that specimen a migrant from Eurasia or from elsewhere in Africa? The model suggested by Xiabo Feng and colleagues is already attracting controversy, but that is nothing new among palaeoanthropologists. Yet it is based on cutting edge phylogeny derived from physical characteristics of hominin fossils: the traditional approach by all palaeobiologists. Such disputes cannot be resolved without ancient DNA or protein assemblages. But neither is a completely hopeless task, for Siberian mammoth teeth have yielded DNA as old as 1.2 Ma and the record is held by genetic material recovered from sediments in Greenland that are up to 2.1 Ma old. The chances of pushing ancient human DNA studies back to the ‘muddle’ in the Middle Pleistocene depend on finding human fossils at high latitudes in sediments of past glacial maxima or very old permafrost, for DNA degrades more rapidly as environmental temperature rises.

See also: Natural History Museum press release. Analysis of reconstructed ancient skull pushes back our origins by 400,000 years to more than one million years ago. 25 September 2025; Bower, B. 2025. An ancient Chinese skull might change how we see our human roots. ScienceNews, 25 September 2025; Ghosh, P. 2025. Million-year-old skull rewrites human evolution, scientists claim. The Guardian, 25 September 2025

A new, ‘bureaucratised’ hominin – Homo bodoensis

Palaeoanthropologists are in a bit of a muddle about the early humans of the Middle Pleistocene (~780 to 130 ka), namely Homo heidelbergensis and H. rhodesiensis. The first was defined in 1907 based on a massive lower jaw or mandible (but no cranium) found near Heidelberg in Germany. Fourteen years later a massively browed cranium (but no mandible) turned up near Kabwe in what is now Zambia (then Northern Rhodesia). That specimen became, in true colonialist fashion, H. rhodesiensis. Since then scientists have unearthed more such highly ‘robust’, ‘archaic’ remains in Africa, Asia and especially Europe: including at least 28 individuals in the Sima de los Huesos (‘pit of bones’), part of the World Heritage Site in the Atapuerca mountains of northern Spain. Do these widespread fossils really represent just two species or do specimens just happen to fit within two broadly similar morphological types? These days, most scientists experience discomfort with a reference to the legacy of Cecil Rhodes, so several sacks full of bones were metaphorically lumped into H. heidelbergensis. So widely dispersed are their sources and their ages covering such a wide span of time that the specimens might be expected contain a diverse range of genetic signatures. Yet only a single specimen from northern Spain, dated around 400 ka, has yielded DNA. The Sierra de Atapuerca provided an even more archaic European dated between 1.2 to 0.8 Ma (Early Pleistocene), from which dental proteins have been extracted. Comparative proteomics have encouraged H. antecessor to be considered as a possible common ancestor for anatomically modern humans (AMH), Neanderthals and Denisovans … and H. heidelbergensis.

A new, simplified model for the evolution of the genus Homo over the last 2 million years (Credit: Roksandic et al Fig 1)

A group of palaeoanthropologists has proposed a way to clear such muddy waters (Roksandic, M. & Radović, P. et al. 2021. Resolving the “muddle in the middle”: The case for Homo bodoensis sp. nov.. Evolutionary Anthropology, v. 30, early-release article 21929; DOI: 10.1002/evan.21929). Their device is to abolish the two previous species and lump together many human remains from the Middle Pleistocene of Africa into a new species named after the Bodo site in the Awash Valley of Ethiopia. It was there that a human cranium bearing characteristics similar to all the African specimens was found in 1976. Originally it was allocated to H. heidelbergensis, but now the composite group of archaic Middle Pleistocene Africans is proposed to be assigned to H. bodoensis. This composite species is also reckoned by the authors to be the ancestor of all surviving, anatomically modern humans. European examples of H. heidelbergensis are to be slotted into an early population of Neanderthals. Since the Denisovans of Asia are only known by DNA from tiny skeletal fragments, the taxonomic rearrangement logically should assign Asian archaic humans to early members of that mysterious but well-defined group. But a spanner in the works is that the sole example of H. heidelbergensis DNA (mitochondrial) – from northern Spain – more closely resembles Denisovans than it that of Neanderthals (see: Mitochondrial DNA from 400 thousand year old humans; Earth-logs December 2013).

There is also a bit of a problem with H. antecessor. There aren’t many specimens, and they are all from Atapuerca. Yet they are a plausible candidate, according to the proteomic analyses, for the most recent common ancestor (MRCA) of all subsequent humans (whatever taxonomists care to call them). But they do not fit in the taxonomic model suggested by Roksandic et al., who reject them as MRCA, on grounds that they are European. They consign them to an anomalous ‘spur’ that petred out in Spain while the real action was in Africa. So what happens if a cranium that bears close similarity to both H antecessor and H. bodoensis pops out of African Early Pleistocene sediments (older than about 700 ka)? There is at least one candidate from ~1 Ma sediments in Eritrea (Abbate, E. and 16 others 1998. A one-million-year-old Homo cranium from the Danakil (Afar) Depression of Eritrea. Nature, v. 393, p. 458-460; DOI: 10.1038/30954), which is said to display ‘a mixture of characters typical of H. erectus and H. sapiens’. And there are others of that antiquity from Ethiopia.

Since the time of Charles Darwin there have been taxonomists who were (and are) either habitual ‘lumpers’ or ‘splitters’. There are more with a propensity for splitting because a new species carries the name of its initiator into posterity! So I expect the paper by Roksandic et al. to raise a cloud of academic dust. Yet taxonomic lumping has its stand-out species in the field of human evolution – H. erectus. A great many ‘archaic-looking’ human remains from the period after ~1.9 Ma until as recently as 200 ka have been dubbed ‘Erects’, giving the group an unsurpassed survival span of over a million years. A few early examples from Africa have been ‘split’ away to give H. ergaster, on taxonomic grounds that some palaeoanthropologists do not fully accept. Yet there are signs of later diversity that ‘splitters’ have, so far, not dared to slice-off from the mainstream consensus. So common are these ‘Erect’ fossils in China, that it is almost state policy that it was they who gave rise to living Han Chinese people! The lumpers are likely to hold sway in the absence of ancient DNA sequencing, which may never be possible outside temperate climates or for ages greater than that of the Spanish H. antecessor. With the knowledge that several anatomically very distinct hominin groups occupied the Earth together at several times in the last 300 ka – think H. floresiensis and H. naledi – it seems likely that the proposed pan-African H. bodoensis may not reflect past reality and the hypothesis needs considerably more testing