Tag: Modern humans

The earliest known human-Neanderthal relations

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The first anatomically modern humans (AMH) known to have left their remains outside of Africa lived about 200 ka ago in Greece and the Middle East. They were followed by several short-lived migrations that got as far as Europe, leaving very few fossils or artefacts. Over that time Neanderthals were continually present. Migration probably depended on windows of opportunity controlled by pressures from climatic changes in Africa and sea level being low enough to leave their heartland: perhaps as many as 8 or 9 before 70 ka, when continuous migration out of Africa began. The first long-enduring AMH presence in Europe began around 47 ka ago.

For about 7 thousand years thereafter – about 350 generations – AMH and Neanderthals co-occupied Europe. Evidence is growing that the two groups shared technology. After 40 ka there are no tangible signs of Neanderthals other than segments of their DNA that constitute a proportion of the genomes of modern non-African people. They and AMH must have interbred at some time in the last 200 ka until Neanderthals disappeared. In the same week in late 2024 two papers that shed much light on that issue were published in the leading scientific journals, Nature and Science, picked up by the world’s news media. Both stem from research led by researchers at the Max Planck Institute for Evolutionary Anthropology in Leipzig, Germany. They focus on new DNA results from the genomes of ancient and living Homo sapiens. One centred on 59 AMH fossils dated between 45 and 2.2 ka and 275 living humans (Iasi, L. M. N. and 6 others 2024. Neanderthal ancestry through time: Insights from genomes of ancient and present-day humans Science, v. 386, p. 1239-1246: DOI: 10.1126/science.adq3010. PDF available by request to leonardo_iasi@eva.mpg.de). The other concerns genomes recovered from seven AMH individuals from the oldest sites in Germany and Czechia. (Sümer, A. P. and 44 others 2024. Earliest modern human genomes constrain timing of Neanderthal admixture. Nature, online article; DOI: 10.1038/s41586-024-08420-x. PDF available by request to arev_suemer@eva.mpg.de ).

Leonardo Iasi and colleagues from the US and UK examined Neanderthal DNA segments found in more than 300 AMH  genomes, both ancient and in living people, by many other researchers. Their critical focus was on lengths of such segments. Repeated genetic recombination in the descendants of those individuals who had both AMH and Neanderthal parents results in shortening of the lengths of their inherited Neanderthal DNA segments. That provides insights into the timing and duration of interbreeding. The approach used by Iasi ­et al­. used sophisticated statistics to enrich their analysis of Neanderthal-human gene flow. They were able to show that the vast majority of Neanderthal inheritance stems from a single period of such gene flow into the common ancestors of all living people who originated outside Africa. This genetic interchange seems to have lasted for about 7 thousand years after 50 ka. This tallies quite closely with the period when fossil and cultural evidence supports AMH and Neanderthals having co-occupied Europe.

Reconstruction of the woman whose skull was found at Zlatý kůň, Czechia. Credit: Tom Björklund / Max Planck Institute for Evolutionary Anthropology.

The other study, led by Arev Sümer,  has an author list of 44 researchers from Germany, the US,  Spain, Australia, Israel, the UK, France, Sweden, Denmark and Czechia. The authors took on a difficult task: extracting full genomes from seven of the oldest AMH fossils found in Europe, six from a cave Ranis in Germany and one from about 230 km away at Zlatý kůň in Czechia. Human bones, dated between 42.2 and 49.5 ka, from the Ranis site had earlier provided mitochondrial DNA that proved them to be AMH. A complete female skull excavated from Czechia site, dated at 45 ka had previously yielded a high quality AMH genome. Interestingly that carried variants associated with dark skin and hair, which perhaps reflect African origins. Neanderthals probably had pale skins and may have passed on to the incomers genes associated with more efficient production of vitamin D in the lower light levels of high latitudes and maybe immunity to some diseases. Both sites contain a distinct range of artefacts known as the Lincombian-Ranisian-Jerzmanowician technocomplex. This culture was once regarded as having been made by Neanderthals, but is now linked by the mtDNA results to early AMH. Such artefacts occur across central and north-western Europe. The bones from both sites are clearly important in addressing the issue of Neanderthal-AMH cultural and familial relationships.

The new, distinct genetic data from the Ranis and Zlatý kůň individuals reveals a mother and her child at Ranis. The female found at Zlatý kůň had a fifth- to sixth-degree genetic relationship with Ranis individuals: she may have been their half first cousin once removed. This suggests a wider range of communications than most people in medieval Europe would have had. The data from both sites suggests that the small Ranis-Zlatý kůň population – estimated at around 200 individuals – diverged late from the main body of AMH who began to populate Asia and Australasia at least 65 ka ago. Their complement of Neanderthal genetic segments seems to have originated during their seven thousand-year presence in Europe. Though they survived through 350 generations it seems that their genetic line was not passed on within and outside of Europe. They died out, perhaps during a sudden cold episode during the climatic decline towards the Last Glacial Maximum. We know that because their particular share of the Neanderthal genome does not crop up in the wider data set used by Iasi et al., neither in Europe and West Asia nor in East Asia. That they survived for so long may well have been due to their genetic inheritance from Neanderthals that made them more resilient to what, for them, was initially an alien environment. It is not over-imaginative to suggest that both populations may have collaborated over this period. But neither survived beyond about 40 ka..

Widely publicised as they have been, the two papers leave much more unanswered than they reveal. Both the AMH-Neanderthal relationship and the general migration out of Africa are shown to be more complex than previously thought by palaeoanthropologists. For a start, the descendants today of migrants who headed east carry more Neanderthal DNA that do living Europeans, and it is different. Where did they interbreed? Possibly in western Asia, but that may never be resolved because warmer conditions tend to degrade genetic material beyond the levels that can be recovered from ancient bones. Also, some living people in the east carry both Neanderthal and Denisovan DNA segments. Research Centres like the Max Planck Institute for Evolutionary Anthropology will clearly offer secure employment for some time yet!

Earliest evidence for rope making: a sophisticated tool

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Even at my age, if I rummage through pockets of various bits of outdoor clothing there’s a good chance I’ll find a handy length of string that I have scavenged at some time. It’s a just-in-case thing, which I learned from my father and grandad. One can hardly imagine a hunter-gatherer not having string or lengths of sinew for that very reason. Cordage has many other uses than merely securing something: bags, mats, nets, snares, fabric, baskets, huts made of sticks and fronds, and even watercraft. Yet archaeological evidence for twine is exceedingly rare. The oldest known string – made of bark fibres – was found wrapped around a stone tool at a 52 to 41 ka Neanderthal site in the Rhône valley 120 km north-west of Marseille. Rope is somewhat more difficult to make as it requires twisting together several lengths of simpler cordage. Once that skill is cracked a rope maker is on the verge of engineering!

The reassembled rope-making tool from Hohle Fels Cave (Credit: Conard & Rots, Fig 2)

In 2015 archaeologists unearthed several pieces of worked mammoth ivory from the Hohle Fels Cave in SW Germany. They were dated to between 40 to 35 ka and associated with Aurignacian stone tools made by modern humans. Fifteen pieces could be fitted together to yield a 20 cm long ‘baton’. First believed to be some kind of ritual object, the fact that 4 circular holes had been bored through the ‘baton’ suggested it must have had some practical use, perhaps for straightening wooden shafts. Then it became clear that each hole was surrounded by spirals of carefully carved, V-shaped notches. Nicholas Conard and Veerle Rots of the University of Tubingen realised that the object may have been used for making rope using a technique known from the Egyptian pharaonic period into medieval times (Conard, N.J. & Rots, V. 2024. Rope making in the Aurignacian of Central Europe more than 35,000 years ago. Science Advances, v. 10, article adh5217; DOI: 10.1126/sciadv.adh5217).

Frame from a movie showing how the tool may have been used to make ropes. The three ‘feeders’ twist foliage clockwise whereas the fourth pulls and imparts an anticlockwise twist to the three stands. (Credit: Conard & Rots, Supplementary material, Fig S15)

After a little practice, four people were able to make sturdy rope using a replica of the tool. Three twisted together fibrous materials, such as the stems and leaves of bulrushes (Typha), and pushed the rough cordage through the intact holes. A fourth person pulled the cordage through and counter-twisted the three strands into rope about 1.5 cm thick – thicker rope would also have required a tool with more holes and more operators. The spiral grooves maintained the initial clockwise rotation of each strand of cordage, so that when all three were twisted together in an anticlockwise sense the counter rotation held the rope together firmly. Remarkably, the small team were able to produce 5 m of rope in 10 minutes. Other common kinds of fibrous plant material, such as linden and willow were used successfully. Incidentally, the tool squeezed edible starch from the foliage of bulrushes. But it seems that this particular rope-making took only performed well for coarse materials. Making rope from finer firbres, such as animal sinew, nettle, flax and hemp would probably have required another design with smaller holes.

A movie of the manufacturing process can be downloaded.

Origin of anatomically modern humans

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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.