Several recent papers present evidence that life was established early on, soon after Earth’s fiery and cataclysmic assembly had ended and its surface had cooled down into a watery world capable of sustaining life. Such an early start implies that life, rather than being unique to Earth may be, if not inevitable, then at least a highly likely outcome here as well as on other Earth-like planets. Give life half a chance and it will rise up and thrive. A result which perhaps shouldn’t come as too big a surprise considering the tenacity with which life has persisted and diversified over the many billions of years since it first emerged. One way to ascertain if life on Earth was a highly likely or inevitable outcome is to find it elsewhere. The recent discovery of thousands of distant planets (exoplanets) orbiting within the watery, and hence potentially habitable zone of their stars is a promising sign that we may be closing in on evidence that life does exists out there in the great beyond. Confirming life on just one exoplanet would imply that our universe is home to a multitude of living worlds peppered across its enormous expanse. This is a mind-boggling concept even if our chances of ever directly interfacing with life elsewhere is remote given the distances involved. As our search for life on distant planets continues, we can also look long and hard for evidence of the earliest life here on Earth. Establishing when life first appeared on Earth can provide us with valuable insights into how life might have come about, but finding convincing evidence of life in the ancient rock record is a difficult task.
The first problem is that most life never leaves even a hint of its existence in the rock record. Life is fragile and readily decomposes such that most living things upon death rapidly vanish, recycled back into the world of non-living elements. Hence, fossil remains of life are rarely preserved in rocks of any age, never mind long ago when the abundance and types of life forms were far more limited than today. The other problem is that older rocks become increasingly difficult to find the further back in time you go. This is because Earth is dynamic, with the movement of its crustal plates (plate tectonics) constantly recycling older rocks into younger rocks. The evidence of life can only be found in the rock record and, therefore, the oldest rocks define the limit of how far back we can potentially detect life. And even for those oldest rocks that we are lucky enough to find and that once harboured fossils, most have since been subjected to intense pressures and temperatures over the dynamic history of their long existence. Such abuse is likely to obscure, if not destroy, whatever original fossil evidence the now transformed rocks may have once contained. Despite these problems, what does the rock record reveal about the earliest life on Earth?
The oldest rocks yet found are around 4 billion years old and occur in Canada and Greenland. We know from the age and composition of meteorites that our solar system formed initially 4.56 billion years ago. It was at this time that Earth’s assembly began by the collision of the many small rocky and metallic bits circling the Sun in our planet’s orbit. Initially gravity pulled in surrounding dust and rock to form small planets (planetissmals) and then these collided gradually to form larger planets. The final, major planetissmal collision that went into the making of Earth occurred 4.44 billion years ago. Our Moon formed from the debris of this collision and the force of the collision transformed Earth into a magma ball, too hot to sustain life. Life could have conceivably been established once the magma ball had cooled and crusted over, and the water vapour had condensed to form the oceans. Conditions on Earth however remained challenging to life as it had to contend with periods of intense bombardment by the sweeping up of the remaining rocky bits. This time of heavy meteorite bombardment is known as the Hadean, named after Hades, god of the underworld. The intense bombardment and the Hadean ended 4 billion years ago to give way to the Archean. To whatever extent life may have started during the Hadean, it was only by the start of the Archean that Earth presented a relatively stable setting for life to persist.
The Hadean (left) was a hellish period of intense meteorite bombardment and vaporised oceans, conditions that were generally not favourable to life, while the Archean world (right) included oceans of water and conditions suitable for the earliest microbial life forms.
The oldest, direct fossil evidence of life is in the form of stromatolites. Stromatolites are mound-shaped structures that form from the activities of microbial mat communities. Stromatolites are common throughout much of the early rock record and some still form today in places like Shark Bay, Western Australia. The minute microorganisms themselves are rarely preserved, but the layered stromatolite structures they build as a result of their activities often are preserved. The distinctive features of stromatolites rule out alternative, non-biological origins for the layered structures, such as the deposition of mineral crusts. The oldest stromatolites were recently discovered in rocks from Greenland 3.7 billion years old (Nutman and others, 2016), significantly older than the previously oldest stromatolites known from Australia dated to 3.48 billion years.
Small conical-shaped mounds (dashed lines) in rocks from Greenland 3.7 billion years old are interpreted to be stromatolites formed by microbial communities (photo by Allen Nutman adapted from Allwood, 2017).
Going back beyond 3.7 billion years, the evidence of life relies on the chemical signature of what is interpreted to be the remains of once living organisms as well as possible fossils. Life on Earth is carbon based and hence most organisms are made up of a significant amount of carbon. For life that grows by taking up carbon directly as CO2, the lighter carbon isotope (carbon 12) is taken up preferentially to the heavier isotope (carbon 13) (the heaviest isotope (carbon 14) is radioactive and has a short life span). The preferential uptake of the light isotope gives life a distinct, negative carbon isotopic composition. When organisms die and their organic matter decomposes, most of the other elements besides carbon, such as nitrogen, phosphorus, oxygen and hydrogen are lost and eventually all that remains is carbon. When heated up under pressure the remaining organic carbon can form the mineral graphite (a soft, grey mineral that is familiar to us as pencil lead). At extreme pressures graphite can transform to diamond. Some have found organic matter in rocks from Greenland greater than 3.7 billion years old that still contains some oxygen, hydrogen, nitrogen and phosphorus because it was preserved as inclusions within the metamorphic mineral garnet (Hassenkam and others, 2017). But in most cases all that remains is pure carbon in the form of graphite. Graphite from rocks in Labrador Canada greater than 3.95 billion years old have carbon isotope values that suggest the carbon was originally part of living organisms. Some of the graphite takes on globular shapes common to some microorganisms (Tashiro and others, 2017). Structures in rocks at least 3.77 billion year old from Quebec Canada interpreted to represent fossil microorganisms suggest that mid-ocean ridge submarine hydrothermal vents or ‘black smokers’ are a potential setting in which early life evolved on Earth (Dodd and others, 2017). Unfortunately, the structures interpreted to be fossil bacteria and the carbon isotope values of graphite interpreted to indicate life processes can both be produced by reactions that do not involve living organisms. Therefore, the indications of life earlier than the 3.7-billion-year-old stromatolites are compelling, but remain ambiguous.
Cluster of globular graphite in quartz chert from Canada is suggestive of fossilised microbial organisms (left, from Tashiro and others, 2017). A modern submarine volcanic vent or ‘black smoker’ is a possible setting where life first emerged on Earth (image from NOAA).
The oldest known rocks are around 4 billion years old, so how can we say anything about earlier periods of Earth history? Some younger rocks contain mineral grains derived from the erosion of older rocks. Zircon is a highly durable mineral that often ends up being eroded out of older rocks but is not destroyed by weathering and ends up being recycled into younger rocks. In fact, the oldest known mineral is zircon dated to as old as 4.38 billion years in rocks from Jack Hills, Western Australia. A small number of these zircon grains have minute inclusions of graphite. The graphite in a zircon grain dated to 4.1 billion years has a carbon isotope signature consistent with a biological origin, but again not unambiguously (Bell and others, 2015). Therefore, the recent evidence pushes back the earliest life on Earth from around 1000 million years to at least 700 million and possibly 300 million years following the final major collisional event 4.44 billion years ago. Assuming it took on the order of 100 million years for Earth to become habitable after the final major collisional event, reduces the time span of life’s emergence to between 600 and 200 million years.
Timeline of early Earth history from its formation as a molten, magma ball, through the hellish Hadean and into the Archean. Oldest direct fossil evidence of life is from stromatolites in rocks 3.7 billion year old and indirect chemical evidence of life comes from rocks around 4 billion year old and from graphite inclusions in zircon minerals 4.1 billion years old.
What is the significance of the suggested narrowing of the time it took life to emerge on Earth? The more rapidly life was established, the less difficult or improbable it would appear to be. The origin of life remains a major unknown. We know that early Earth likely had an enormous diversity of chemical compounds to work with including amino acids, which are the building blocks of all life today. But whether life was inevitable or even highly likely to come about is open to debate, because it remains unclear how these compounds became organised into self-replicating, evolving organisms. It could be that the emergence of life is simply too slow a process for us to replicate in the lab. Even the simplest of life forms, bacteria, involve an incredibly complex array of biochemical reactions and processes that would have taken time to evolve from the diverse pool of chemical compounds available. Although less than previously thought, several hundred million years is still a long span of time over which life could have gradually emerged.
It seems unlikely that the rock record will allow us to refine the timing much more or to push it back much further. Thus, the implied ease at which life can emerge on a place like Earth will perhaps have to wait for the discovery of life on another planet. Just what form life will take on other planets is unknown, but if at all like Earth, life is most likely to be dominated by diverse yet small, simple microbial organisms. Perhaps quick to get started, life on Earth appears to have remained fairly simple for a long period of time. It took around a billion years before the more complex eukaryotic cells evolved and another two billion years or so after that before animals evolved. The delay in the evolution of animals has been attributed to the need of an oxygen-rich atmosphere. For the latest ideas on what may have controlled oxygen levels in the atmosphere and how the level became high enough for animals, check out my next blog update #6: First Animals.
Allwood, A.C., 2016. Evidence of life in Earth’s oldest rocks. Nature 537, 500-501 (doi:10.1038/nature19429).
Bell, E.A., and others, 2015. Potentially biogenic carbon preserved in a 4.1 billion-year-old zircon. PNAS 112, 14518–14521 (www.pnas.org/cgi/doi/10.1073/pnas.1517557112).
Dodd, M.S., and others 2017. Evidence for early life in Earth’s oldest hydrothermal vent precipitates. Nature 543, 60-64 (doi:10.1038/nature21377).
Hassenkam, T., and others, 2017. Elements of Eoarchean life trapped in mineral inclusions. Nature 548, 78-81 (doi:10.1038/nature23261).
Nutman, A.P., and others, 2016. Rapid emergence of life shown by discovery of 3,700-million-year-old microbial structures. Nature 537, 535-538 (doi:10.1038/nature19355).
Tashiro, T., and others, 2017. Early trace of life from 3.95 Ga sedimentary rocks in Labrador, Canada. Nature 549, 516-518 (doi:10.1038/nature24019).
Australia is home to some of our species’ most ancient roots outside of Africa. When the first of our human (Homo) lineage arrived in Australia has long been debated. Although early members of our lineage (Homo erectus, for example) were living nearby on the island of Java as early as 1.7 million years ago, it was only much later that humans entered Australia. Dated archaeological sites suggest that our species, Homo sapiens was the first to arrive by around 50 thousand years ago (50 ka) and that we had become widespread throughout the continent by 45 ka (Hamm and others, 2016). This chronology generally fits with the proposed timing of the ‘Great Expansion,’ when our species rapidly spread out of Africa around 60 to 50 ka and effectively conquered the world. Our species had earlier forays out of Africa prior to the Great Expansion, but these never appear to have amounted to much. In my book Human Origins I refer to those who left Africa prior to the Great Expansion as anatomically modern humans (AMHs) and those that left as part of the Great Expansion as people having cultures on a par with modern hunter-gatherers. Our species evolved in Africa 200 to 160 ka, but appears to have only slowly acquired cultures equivalent to modern hunter-gatherers between 100 and 70 ka while in Africa. This may explain, in part, why earlier exits were relatively unsuccessful: the Great Expansion had to wait until modern hunter-gatherers had emerged in Africa and their movement beyond Africa, in turn, had to wait until the Sahara-Arabian Desert became sufficiently green to let them out 60 to 50 ka. However, a recent study by Clarkson and others (2017) proposes that modern people had arrived in Australia by at least 59.3 ka and possibly as early as 70 ka. Such an early arrival of people in Australia would be at odds with the Great Expansion scenario.
Going global: possible pathways and timing of the Great Expansion, when modern people conquered the world.
Humans could expand into Southeast Asia when sea level was lower (pale blue areas of Sunda) but had to island-hop their way through Wallacea to reach the connected landmasses of New Guinea and Australia (Sahul).
Therefore, it would appear that the first arrivals in Australia were AMHs from an earlier exit out of Africa. As elsewhere in Eurasia, the AMHs who arrived in Australia had a relatively subdued impact and were largely displaced by the later arrival of modern hunter-gatherers as part of the Great Expansion who reached Australia by around 50 ka. This Great Expansion scenario is supported by genetic studies which indicate that all people today outside of Africa descend from a single population that exited out of Africa and that they acquired DNA from intermingling with Denisovans and Neanderthals along the way between 53 to 45 ka. DNA studies of indigenous Australians (aborigines) indicate that those who arrived with the Great Expansion rapidly colonized the continent by 45 ka (Tobler and others, 2017). To whatever extent earlier expansions of our species may have taken place prior to the Great Expansion, none feature strongly in either the archaeological or genetic evidence, their existence appears to have been swamped out by the rapid peopling of the world during the Great Expansion. However, the earlier forays of our species out of Africa were perhaps not completely erased, with some genetic studies suggesting that a few percent of the DNA from these earlier expansions survives in modern populations (Pagani and others, 2016).
Aubert, M., and others, 2014. Pleistocene cave art from Sulawesi, Indonesia. Nature 514, 223-227. doi:10.1038/nature13422
Clarkson, C., and others, 2017. Human occupation of northern Australia by 65,000 years ago. Nature 547, 306-310. doi:10.1038/nature22968
Gibbons, A., 2017. The first Australians arrived early. Science 357, 238-239. doi: 10.1126/science.357.6348.238
Hamm, G., and others, 2016. Cultural innovation and megafauna interaction in the early settlement of arid Australia. Nature 539, 280-283. doi:10.1038/nature20125
Marean, C.W., 2017. Early signs of human presence in Australia. Nature 547, 285-287.
Pagani, L., and others, 2016. Genomic analyses inform on migration events during the peopling of Eurasia. Nature 538, 238-241. doi:10.1038/nature19792
Tobler, R., and others, 2017. Aboriginal mitogenomes reveal 50,000 years of regionalism in Australia. Nature 544, 180-184. doi:10.1038/nature21416
Westaway, K.E., and others, 2017. An early modern human presence in Sumatra 73,000–63,000 years ago. Nature 548, 322-325. doi:10.1038/nature23452
© John S. Compton (www.johnscompton.com)
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A recent study presents evidence that members of our human (Homo) lineage were in North America around 130 thousand years ago (Holen and others, 2017; Wade, 2017a). This is a shocking claim because it is more than 100 thousand years before the previously established timing of 14 thousand years ago for when humans first entered the Americas. This latest report is not the first to argue for a much earlier presence of humans in the Americas, but it provides by far the most compelling and best dated evidence yet.
The evidence consists of scattered mastodon bones lying immediately adjacent to several large stones. The bed in which the bones and stones occur were recovered from a 12-m-thick succession of river deposits discovered at a construction site near San Diego, California. The mastodon is a distant relative of elephants and was common in North America (along with the woolly mammoth and other large animals) up until people hunted them to extinction by around 12 thousand years ago. The authors of the study argue that the physical damage of some mastodon bones and associated stones indicate that the stones were used as hammerstones and anvils to break open the large mastodon bones. Breaking of the bones was done most likely to access the oozing, nutrient-rich marrow inside. The large stones were locally sourced but, oddly, none was modified or shaped in any way by removal of smaller stone flakes. Although no human bones were found at the site, it is assumed that humans were responsible because no other animal capable of smashing large mastodon bones with large stones is known to have lived at this time in the Americas.
The site was determined to be 130.7 ± 9.4 thousand years old based on the decay of the radioactive element uranium contained within the bones. There was no organic carbon left in the bones to date using radiocarbon methods and the application of optically stimulated luminescence (OSL) indicated that the sediment at the site was deposited at least 60 thousand years ago. The age uncertainty of plus/minus nearly ten thousand years reflects, in part, the model assumptions made in using the uranium-series disequilibrium method. However, the uranium-derived ages appear to be robust and indicate that the deposit most likely formed sometime between 140 and 120 thousand years ago.
The lack of human bones, as well as any other stone tools or cultural artefacts besides the hammerstones and anvils, make it difficult to say which member of our human lineage was active at the site. It is certainly conceivable that members of our lineage living in Eurasia may have crossed over to North America when the Beringia land bridge was exposed. The Beringia land bridge today is flooded by the Bering Sea, but the lowering of sea level at times in the past was sufficient to expose the Bering Sea as a land bridge connecting Eurasia and North America. For example, the Beringia land bridge could have been crossed roughly 134 to 131 thousand years ago, within the age window of the mastodon site. Any humans living in eastern Siberia at that time may have made the journey across on foot without necessarily making use of boats.
Siberia was connected to North America periodically when sea level was lowered by major ice build up. Humans living in Siberia could have crossed over to North America either by boat along a coastal route or on foot overland through ice-free corridors.
The highly successful crossing 14 thousand years ago was part of the Great Expansion of behaviourally modern people who left Africa around 60 to 50 thousand years ago. There are numerous archaeological sites that show modern people had entered and become widespread throughout the Americas, reaching the southern coast of Chile by around 14 thousand years ago. The timing of initial entry into the Americas is thought to be mostly determined by when people living in the Far East and eastern Siberia could cross over the Beringia land bridge connecting Eurasia and North America during the Last Glacial Maximum when sea level was lowered in response to the build-up of major ice sheets. Passage into North America from Beringia was delayed until the large ice sheet blocking the way had started to melt back with the onset of warmer climates 18 to 14 thousand years ago. There was a relatively brief window to pass over the land bridge before it was flooded by the rising sea as the ice sheets quickly melted. Most are sceptical that humans had crossed over before 14 thousand years ago, with the current debate centred on when people crossed over, where they came from and whether they travelled by canoe along a coastal route or overland on foot through ice-free corridors that opened as the large Laurentide ice sheet melted back (Wade, 2017b).
It is not too far-fetched that some of our ancestors living in Eurasia might have crossed over to the Americas much earlier than the well-documented crossing of people by 14 thousand years ago. This is because the Beringia land bridge was repeatedly exposed as Earth cycled through glacial and interglacial periods over the last million years. Any of our ancestors adapted to living at relatively high latitudes may have inadvertently crossed over Beringia in pursuit of game and, once across, they could expand and fill the virgin American landscapes.
Sea-level cycles over the last million years and the periodic exposure of the Beringia land bridge in the transition from glacial to interglacial periods when animals (including humans) may have crossed over to North America (brown columns). The mastodon archaeological site reported from southern California implies humans crossed over sometime prior to 134 to 131 thousand years ago during the MIS 6 glacial to MIS 5 interglacial transition (third brown column on the right) when Neanderthals and Denisovans, but probably not our species (Homo sapiens) or the ‘hobbit’ (H. floresiensis), were living at high latitudes in Eurasia.
Could it have been our species, Homo sapiens, who crossed over? This seems unlikely because, although our species had appeared in Africa by around 200 to 160 thousand years ago, the earliest evidence of when we left Africa is 131 to 113 thousand years ago (MIS 5). After crossing over, our species appears to have largely been confined to the Middle East region. There is, as yet, no evidence that they had expanded into Siberia as early as when the Beringia land bridge to the Americas was exposed 134 to 131 thousand years ago. So, if not our species, then what other member of our lineage may have crossed over prior to 140 to 120 thousand years ago?
We know that Neanderthals, Denisovans and the ‘hobbit’ (Homo floresiensis) were all living in Eurasia at this time. Homo erectus was widespread throughout Eurasia even earlier, but does not appear to have lived at high enough latitudes, above 40°N, to have crossed over the Beringia land bridge located at latitudes above 55°N. The ‘hobbit’ is only known from the Indonesian island of Flores where it lived from 700 up until 50 thousand years ago, whereas Neanderthals and Denisovans are known to have lived at high latitudes, including Siberia. However, it is unclear which of the two crossed over the Beringia land bridge because the only stone tools (hammerstones and anvils) yet to be recovered from the site are not shaped in any way. Almost all contemporaneous stone tools documented in Eurasia (and Africa) were intentionally shaped by the removal of stone flakes. The lack of shaped stone tools is an unusual, and difficult to comprehend, aspect of the mastodon site.
Another surprising aspect about the mastodon site besides its lack of shaped stone tools, is that there has been so little convincing evidence of an earlier human presence in the Americas before now. If humans did managed to cross over, then it is predicted that they would have rapidly spread into the virgin landscapes, landscapes never before occupied by humans and full of large animals relatively easy to hunt. The Americas are two enormous continents no more difficult for humans to thrive in than Eurasia. So why are traces of humans living there so difficult to see in comparison to the record in Eurasia? Has the abundance of archaeological sites younger than 14 thousand years old obscured older, less abundant evidence? Perhaps if people dig a bit deeper and consciously look for it, an older record of humans in the Americas will be revealed. Now that the first compelling site has been discovered, perhaps more will follow.
Holen, S. R., and others, 2017. A 130,000-year-old archaeological site in southern California, USA. Nature 544, 479–483. doi:10.1038/nature22065
Wade, L., 2017a. Claim of very early humans in Americas shocks researchers. Science 356, 361. doi: 10.1126/science.356.6336.361
Wade, L., 2017b. On the trail of ancient mariners. Science 357, 542-545.
© John S. Compton (www.johnscompton.com)
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Update #2 to Human Origins: How diet, climate and landscape shaped us
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The age of the fossil-rich Homo naledi fossil site within the Rising Star cave system in the Cradle of Humankind World Heritage Site near Johannesburg, South Africa was frustratingly unknown until recently. The exceptionally large number of fossil bones scattered on the cave floor proved difficult to date, but an international team of scientists has applied several dating techniques (optically stimulated luminescence, uranium/thorium and palaeomagnetism) to constrain the age of the deposit to between 414 and 236 thousand years old (Dirks and others, 2017). This age is supported by the estimated age of several fossil teeth from the deposit, independently dated to between 335 and 183 thousand years old using a combination of uranium series and electron spin resonance (US-ESR) methods. The US-ESR methods directly date the fossils, but rely on a number of complex model assumptions that result in a large amount of uncertainty. Although not terribly precise, these ages are considered fairly robust and are surprisingly young for fossils whose features (or traits) suggest that they are much older. Prior to the age determinations, many estimated that the fossils, given their mix of australopith and early Homo features, would date to around when our genus Homo first appeared in the fossil record between 3 and 2 million years ago (Ma). How, then, is such a young age explained for fossils that retain so many old features?
A mosaic of features
One of the striking aspects of the Homo naledi fossils is the odd mix or mosaic of features they display. The amazingly rich fossil find from the Rising Star cave system includes a total of over 1500 bones from the Dinaledi Chamber alone (Berger and others, 2015), with more bones recently discovered in the separate Lesedi Chamber (Hawks and others, 2017). All of the bones recovered from both caves are considered to belong to Homo naledi and comprise a minimum of 15 individuals. Such a large number of bones provides a fairly complete skeleton of Homo naledi who stood 1.4-1.6 m high and weighed 40-55 kg. One of the most notable features is the small size of the skull, having an interior volume (endocranial capacity) of between 460 and 610 cc. This range in volume is based on three skulls and is intermediate between the mean skull size of the australopiths and the earliest Homo species for which skulls are available that date to around 2 Ma. Such a small skull suggested that Homo naledi represented one of the earliest members of our genus Homo, which branched from the australopiths around 2.8 to 2.3 Ma, based on fossil teeth and jaws from East Africa (Villmoare and others, 2015). In contrast, its foot shares many features similar to ours. Comparing Homo naledi to other species is difficult to do because for most other species there are simply not enough fossil bones to compare. However, overall, Homo naledi much more closely resembles early Homo (H. habilis and H. erectus) than it does us (H. sapiens) or our predecessor species (‘archaic’ H. sapiens). The close resemblance to early Homo suggested to many that the age of the deposit would be similar in age to when early Homo appeared circa 2.5 Ma and not the reported age of less than 0.5 Ma.
Skull of Homo naledi (LES1) from the Lesedi Chamber (left; scale bar 5 cm) and the digital reconstruction of the endocranial volume of 610 cc, scale sphere is 10 mm (Hawks and others, 2017).
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The most likely explanation is that Homo naledi represents one of the earliest members of our Homo lineage and that it managed to retain many features of early Homo up until at least 414 to 236 thousand years ago. While retaining many of its early features, it also appears to have acquired features that closely resemble later features, which either evolved independently (convergent evolution) or were acquired through interbreeding (hybridization) with other, later-evolved Homo species (but probably not our species, which only appeared by around 200 to 150 thousand years ago).
What is remarkable is that Homo naledi persisted for so long in a region occupied by other, later-evolved Homo species. For example, the skull from the Florisbad fossil site is thought to represent our predecessor species and was likely contemporary with Homo naledi, the two living within several hundred kilometres of one another. One possible explanation of their co-existence is that they occupied distinctly different habitats. Although their feet and aspects of their hands are similar to ours, Homo naledi’s fingers are curved. Curved fingers suggest that they were adapted for living in and moving about in trees. Therefore, they may have resided within heavily treed habitats, such as forest canopies, whereas our predecessor species was living primarily in more open grassland and savannah habitats. Although such niche partitioning may explain the co-existence of different species of Homo, it is remarkable that a species with so many early features, including such a small brain, managed to survive until just prior to when our species Homo sapiens evolved onto the scene.
Homo naledi is not the only member of our Homo lineage who managed to persist over such a long period of time. Homo erectus, for example, managed to survive in Asia long after they had become locally extinct in Africa, surviving up until around 300 thousand years ago in China and Java. And, in many respects, the suite of unusual features of Homo naledi reflect those of Homo floresiensis, the ‘hobbit”, which also retains features of early Homo (H. habilis and H. erectus) and lived up until just 50 thousand years ago on the island of Flores (Sutikna and others, 2016). The persistence of H. floresiensis on the somewhat remote island of Flores seems more plausible than a group within the African continent, but perhaps this reflects the fact that groups in Africa were adapted to specific habitats that effectively isolated them from other groups. Population densities were likely low and, along with the diversity of habitats, may have facilitated the survival of earlier groups for long periods of time. More recently evolved species might have been widely dispersed in part because of their big brain, sophisticated tools and control of fire, but were perhaps spread thinly enough over the landscape to have permitted pockets of earlier evolved groups to hang on. What the hobbit and Homo naledi seem to indicate is that among the more recently evolved members of our lineage, older groups managed to persist, either within distinct habitat or niche holdouts ̶ perhaps culturally as much as physically isolated from other groups. The fossil record is so limited it may have hidden from us or we may have tended to underestimate the amount of variability in features, such as brain and body size that existed in the past.
Homo naledi culture?
Typically an archaeological site has hundreds to thousands of stone artefacts but very few if any fossil bones of those who made the artefacts. And whether or not any bones of the makers of the stone tools are found, it is common to find the bones of other animals at many archaeological sites. Hence, the Rising Star cave sites present the most unusual case: many bones of Homo naledi not in association with any stone tools or other cultural artefacts, nor any other large animal bones. Hence, although we know a lot about what Homo naledi looked like, we have very little idea of what they made or what other animals they lived among.
This lack of context makes it difficult to know much about the habitat in which they lived and how they lived. They most clearly did not live in the deep caves where they ended up as fossils. It is conceivable that they fell into or were washed down into the caves through surface openings connected to deep cave chambers. But in that case we would expect other large animals to have fallen in or been washed into the caves along with them. Some have proposed that they were intentionally disposed of into cave openings and that this disposal may indicate a type of ritual burial (Berger and others, 2017). Ritual burial is a cultural behaviour that has so far only been associated with our species, with the earliest hints (mortuary defleshing) dating to around 160 thousand years ago, and proper burials with grave goods not until around 100 thousand years ago. It is possible they disposed of their dead into the caves as a form of good housekeeping, but it is hard to imagine that small-brained Homo naledi had the mental ability to practice ritual burials, and evidence to substantiate ritual disposal into the caves remains lacking.
The complete absence of stone tools makes it difficult to know what stone tools, if any, were used by Homo naledi. They possess the wrists and hands capable of making and using stone tools, but did they? The age of the site falls within the Middle Stone Age (MSA), a time of regionally diverse stone tool industries throughout Africa. Some have suggested that Homo naledi may have been the maker of some of these stone tools (Berger and others, 2017), but so far there is no direct evidence to support this idea. The appearance of stone tool use has been dated as far back as 3.3 Ma and associated with australopiths having brains similar to or smaller sized than Homo naledi, but these early stone tools are a far cry from the diversity and sophistication of MSA stone tools that existed throughout much of Africa by 300 thousand years ago. Hopefully future finds of Homo naledi in association with cultural artefacts will shed some light on where and how they lived.
Berger. L., and others, 2017. Homo naledi and Pleistocene hominin evolution in subequatorial Africa. eLife 2017;6:e24234. DOI: 10.7554/eLife.24234
Berger, L., and others, 2015. Homo naledi, a new species of the genus Homo from the Dinaledi Chamber, South Africa. eLife 2015;4:e09560. DOI: 10.7554/eLife.09560
Dirks, P., and others, 2017. The age of Homo naledi and associated sediments in the rising star Cave, South Africa. eLife 6:e24231. doi: 10.7554/eLife.24231
Harmand, S., and others, 2015. 3.3-million-year-old stone tools from Lomekwi 3, West Turkana, Kenya. Nature 521, 310–318.
Hawks, J., and others, 2017. New fossil remains of Homo naledi from the Lesedi Chamber, South Africa. eLife 6:e24232. DOI: 10.7554/eLife.24232
Sutikna, T., and others, 2016. Revised stratigraphy and chronology for Homo floresiensis at Liang Bua in Indonesia. Nature 532, 366–369.
Villmoare, B., and others, 2015. Early Homo at 2.8 Ma from Ledi-Geraru, Afar, Ethiopia. Science 347, 1352–1355.
A 3.3 Ma Lomekwian stone tool (left; Harmand and others, 2015) is a far cry from regionally diverse MSA stone tools throughout Africa 300-100 thousand years ago (right).
Update #1 to Human Origins: How diet, climate and landscape shaped us
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© John S. Compton