Advances in hominin evolution

For decades, most of the news concerning our deep ancestry emerged from discoveries in sub-Saharan Africa at sites in Zambia, Tanzania, Kenya, South Africa, Ethiopia. The first week of 2026 decisively shifted that focus northwards to Chad and Morocco in two separate publications.

In 2002 ago the world of palaeoanthropology was in turmoil following the first discovery of fragments of what was then thought to be a hominid, or great-ape, cranium in Chad dated at around 7 Ma ago (Brunet, M. and 37 others 2002. A new hominid from the Upper Miocene of Chad, central Africa. Nature, v. 4418, p. 145-151;DOI:10.1038/nature00879). When pieced together the cranium looked like a cross between that of a chimpanzee and an australopithecine. Some suggested that the creature may have been a ‘missing link’ between the hominids and hominins; perhaps the ultimate ancestor of humans. Sahelanthropus tchadensis (nicknamedToumaï­ or ‘hope of life’ in the local Goran language) was undoubtedly enigmatic. The ‘molecular-clock’ age estimate for the branching of hominins from a common ancestor with chimpanzees was, in 2002, judged to be two million years later the dating of Sahelanthropus, so controversy was inevitable. Another point of contention was the size of Sahelanthropus’s canine teeth: too large for australopithecines and humans, but more appropriate for a gorilla or chimp. Moreover, Toumaï­ showed no indisputable evidence for having been bipedal. The Chadian site subsequently yielded three lower jaw bones and a collection of teeth, a partial femur (leg bone) and three fragmentary ulnae (forearm bones). The finds suggested that as many as five individuals had been fossilised. The femur gave an unresolved hint of an upright gait, yet the ulnas suggested Toumaï­ might equally have been arboreal; as could also be said for the australopithecines.

Reconstructed skull of Sahelanthropus tchadensis. (Credit: Didier Descouens, University of Toulouse)

All the limb bones of Toumaï­have now been anatomically compared with those of hominins and apes (Williams S.A. et al. 2026. Earliest evidence of hominin bipedalism in Sahelanthropus tchadensis. Science Advances, v. 12, article eadv0130; DOI: 10.1126/sciadv.adv0130). Scott Williams of New York University and co-workers from other US institutions show that although the leg bones are much the same size as those of chimpanzees, their proportions were more like those of hominins. They also showed features around the knees and hips needed for bipedalism and an insertion point for a tendon for the gluteus maximus muscle (buttock) vital for sustained upright locomotion, similar to the femurs of Orrorin tugenensis (see: Orrorin walked the walk; May 2008) and Ardipithecus ramidus. Unfortunately, an intact Sahelanthropus cranium showing a foramen magnum – where the skull attaches to the spine – continues to elude field workers. Its position distinguishes upright gait definitively.

See also: This ancient fossil could rewrite the story of human originsScience Daily, January 3, 2026)

The second new advance concerns the joint ancestry of Neanderthals, Denisovans and anatomically modern humans (AMH), whose ancient genetics crudely suggest a last common ancestor living between 765 to 550 ka. This had previously been attributed to Homo antecessor found in the Gran Dolina cave at Atapuerca in northern Spain, roughly dated between 950 ka and 770 ka. (Incidentally, Gran Dolina has yielded plausible evidence of cannibalism). A novel possibility stems from hominin fossils excavated from a cave in raised-beach sediments near Casablanca in Morocco (Hublin, JJ. and 28 others, 2026  Early hominins from Morocco basal to the Homo sapiens lineageNature, v. 649 ; DOI: 10.1038/s41586-025-09914-y). The fossil-bearing sediments contain evidence for a shift in the Earth’s magnetic field (the Brunhes–Matuyama reversal) dated at 773 ka, much more precisely than the Atapuerca age span for H. antecessor. Jean-Jacques Hublin of CNRS in Paris and his multinational colleagues report that the fossils are similar in age to H. antecessor, yet are morphologically distinct, displaying a combination of primitive traits and of ‘derived features reminiscent of’ later Neanderthal, Denisovan and AMH fossils. The differences and shared features suggest that there may have been genetic exchanges between the Moroccan and Iberian population over a considerable period. The most obvious route would have been across the Straits of Gibraltar, but would have required some kind of water craft.  An important question is ‘which population gave rise to the other?’

Artistic reconstruction of a juvenile Homo antecessor, Based on skeletal remains from Gran Dolina Cave

Larger and more robust hominin remains in Algeria dated at 1,000 ka – H. heidelbergensis? – resemble those found near Casablanca. They may have evolved to the latter. Similar possible progenitors to Iberian Homo antecessor have yet to be found in Western Europe. Homo erectus appeared in Georgia and Romania between 2.0 and 1.9 Ma, but the intervening million years or more have yielded no credible European forebears of H. antecessor. For the moment, incursion of a North African population into Europe followed by sustained contact is Hublin et al’s favoured hypothesis, rather than a European origin for Homo antecessor. For Neanderthals and Denisovans to have originated from such an African group, as has been suggested, requires finds of African fossils with plausible resemblance to what are predominantly Eurasian groups. The Iberian population migrated far and wide in Western Europe, as witnessed by stone tools and footprints dating to between 950 to 850 ka in eastern England. So it is equally possible that the Iberian group were progenitors of Neanderthals and Denisovans in Eurasia itself. At least for the moment, ancient genomes of the two H. antecessor groups are unlikely to be found in either Iberian or African fossils of the same antiquity. But, as usual, that will not stifle debate: a resort to the adage ‘absence of evidence is not evidence of absence’ seems appropriate to several research teams!

The oldest anatomically modern human fossils dated at ~300 ka, were also discovered in Morocco (see: Origin of anatomically modern humans, June 2017). Their isolation in the NW corner of the African continent poses a similar conundrum, as since then such beings went on to occupy wide areas of sub-Saharan Africa and then the world.

Origin of anatomically modern humans

How evolution proceeds and species arise are affected by many different processes. But, if members of every generation of the clade that led from the probable common ancestor of ourselves, Neanderthals, Denisovans and other hominins of the last 700 ka or so – widely thought to have been Homo heidelbergensis­ – were found as perfectly preserved fossils they would show gradually shifting anatomical features that from time to time and place to place would diverge to lead to different species. If, also, every specimen was accurately dated then there would be the last part of the human evolutionary bush laid out in a 3-D graphic. That is never going to be possible, of course. Human fossils are rare and there are few of them that are well-preserved. So the field of human origins throws up surprises on a regular basis, and if palaeoanthropologists were more dogmatic than most of them actually are there would be equally regular, public displays of the eating of hats.

As regards early modern H. sapiens, fossils from a couple of sites in Ethiopia have been the oldest known, at between 160 to 195 ka, for the last 15 years. However, in the 1960s quarry workers at Jebel Irhoud in SW Morocco exposed the infill of a cave network in which were found numerous items of the Levallois stone-tool technology, some human bone fragments that included a brain case and many dismembered and cut bones of prey animals. Initially they were thought to date from about 40 ka and to represent an African form of Neanderthals. Subsequently, re-evaluation of the remains revealed a greater likelihood that they were from modern humans, but too young to be of great interest. An upgraded date of ~160 ka caused them to be considered  as peripheral to the core group of Ethiopian early modern humans. DNA analyses then suggested modern humans to have split from Neanderthals about 500 ka ago. Members of the French-Moroccan team that did the original work, accompanied by other scientists, recently re-excavated the site and exhumed a much richer fossil haul that pin-pointed an anatomically modern human (AMH) provenance, albeit with some archaic characteristics (Hublin, J.-J. and 10 others, 2017. New fossils from Jebel Irhoud, Morocco and the pan-African origin of Homo sapiens. Nature, v. 546, p. 289-294; doi:10.1038/nature22336), which can be referred to as ‘pre-modern’ H. sapiens. The bombshell stemming from their work was the precise dating of the fossils and their stratigraphic context by other members of the team (Richter, D. and 11 others. The age of the hominin fossils from Jebel Irhoud, Morocco, and the origins of the Middle Stone Age. Nature, v. 546, p. 293-296; doi:10.1038/nature22335), which yielded 315±34 ka from fire-heated flint fragments and 286±32 ka from a human tooth. Both dates are far older than the previously accepted maximum of 200 ka for AMH.

The early evolution of fully modern humans seems to have spanned the whole of Africa, rather than being set in an Ethiopian heartland, a view partly supported by a fragmentary 260 ka fossil from South Africa bearing close resemblance to the Moroccan individuals. Interestingly, Levallois stone tools, as their name suggests, are widespread in both Africa and Europe at around 300 ka, although that is not proof that AMH migrated out of Africa around 300 ka, for Neanderthals may also have been using a similar flint flaking method (another space to be watched).

See also:  Stringer C. & Galway-Witham, J., 2017. On the origin of our species.  Nature, v. 546, p. 212-215; doi:10.1038/nature 546212a.

You can find more information on migration of modern humans here.