john hawks weblog

paleoanthropology, genetics and evolution

stone tools

  • Cutmarked bones from Dikika critiqued

    Wed, 2010-11-17 00:18 -- John Hawks

    Manuel Dominguez-Rodrigo, writing with my University of Wisconsin colleagues Travis Pickering and Henry Bunn, has challenged the interpretation that two bovid bones from Dikika bear cutmarks made by hominins [1]. I wrote about the Dikika cutmark claims earlier this year (Australopithecus afarensis used stone tools). The new paper is a strong critique of that earlier work.

    Our taphonomic configurational approach to assess the claims of A. afarensis butchery at Dikika suggests the claims of unexpectedly early butchering at the site are not warranted. The Dikika research group focused its analysis on the morphology of the marks in question but failed to demonstrate, through recovery of similarly marked in situ fossils, the exact provenience of the pub- lished fossils, and failed to note occurrences of random striae on the cortices of the published fossils (incurred through incidental move- ment of the defleshed specimens across and/or within their abrasive encasing sediments). The occurrence of such random striae (some- times called collectively “trampling” damage) on the two fossils provide the configurational context for rejection of the claimed butchery marks. The earliest best evidence for hominin butchery thus remains at 2.6 to 2.5 Ma, presumably associated with more derived species than A. afarensis.

    These authors are experts on cutmarks, both from their work on Oldowan faunal assemblages and from experimental work where they have controlled the actual circumstances of cutmarking, trampling and weathering. Their critique of the two Dikika bones takes two main paths:

    1. The surfaces of the bones themselves are relatively poorly preserved, with evidence of "trampling" modification and subadult status for one specimen and evidence of "moderate weathering" on the other. The matrix containing the bones was highly abrasive, making spurious marks more likely. This would make it difficult to get clear results even in an experimental context.

    2. The purported cutmarks themselves are similar to marks that occur in bones subject to trampling damage. Dominguez-Rodrigo and colleagues argue that some of these marks are more diagnostic of trampling than of cutting or hammerstone damage.

    The authors do not say they have disproven the hypothesis that A. afarensis cut on these bones with naturally-occurring stones, but they clearly question whether such a hypothesis is credible:

    The Dikika “butchery mark” evidence does not, however, withstand peer scrutiny undertaken from an actualistic perspective and with a configurational approach. Our approach in assessing the Dikika claims was intentionally conservative: the claims are extraordinary because of their singularity and because of the inferred age of the fossils. Thus, natural processes of bone modification need to be eliminated before precluding nonanthropogenic origin(s) for the surficial marks on DIK-55–2 and DIK-55–3. High probability trampling damage on both specimens does not allow for this elimination and, again, taking our contextualized, maximally conservative position, forces us to reject even marks A1 and A2, the two morphologically strongest claims of cutmarks on DIK-55–2.

    Their discussion emphasizes that, in their view, a hypothesis that an unusual tool type was responsible for cutmarks should be accompanied by experimental or actualistic evidence concerning the effects of that tool type. I think that for discoveries as potentially important as this, it is very reasonable for reviewers to expect such evidence will be provided. Also, a full statistical workup of other faunal bones from the site would be worthwhile. If the matrix really is abrasive and readily gives rise to trampling scratches, these should be evident in a wider distribution of bone from the site.

    But for the moment, it looks like we should continue to treat cautiously claims of very early stone tool use. Possibly further comparisons will back up the hypothesis of cutmarks with more evidence. Since it took only three months from the initial publication of the Dikika evidence to this response, maybe we won't have to wait long for more comparisons!


    References

    1. Dominguez-Rodrigo M, Pickering TR, and Bunn HT. 2010. Configurational approach to identifying the earliest hominin butchers. Proceedings of the National Academy of Sciences [Internet] 107:20929–20934. Available from: http://dx.doi.org/10.1073/pnas.1013711107
    Synopsis: 
    The claim of stone tool use by A. africanus comes under fire.
  • Sink Australopithecus!

    Mon, 2010-08-16 14:36 -- John Hawks

    Dennis Etler has been going great guns on his blog, Sinanthropus.

    Last week's article claiming cutmarks on A. afarensis-aged fauna from Dikika (Australopithecus afarensis used stone tools) got Dennis to write a provocative post: "Its time to sink the genus Australopithecus redux."

    Either A. afarensis should be revised to H. afarensis or the possibility must be entertained that the Woranso-Mille individual and the maker of the stone tool cut marks at Dikika represent a new previously unknown species of Homo (perhaps H. antiquus Ferguson 1984) that lived contemporaneously with A. afarensis.

    He mentions the relevance of the Woranso-Mille skeleton (which I haven't yet gotten to here) and A. sediba for this conclusion. Etler's earlier post, "It's time to sink the genus Australopithecus" goes into more detail on these remains.

    To me, the key question is whether Homo as we understand it now (including H. habilis) is polyphyletic. One way to escape this question is to narrow our genus, placing H. habilis and its ilk into Australopithecus. But Australopithecus defined broadly in this way is almost certainly paraphyletic. And that's without considering the issue of robust australopithecines. I can see why one might follow Ernst Mayr and stick them all in Homo.

  • Mailbag: The capuchin australopithecines

    Thu, 2010-08-12 12:20 -- John Hawks

    Re: australopithecine tools:

    Eh, now that I think about it, your bonus prognostication doesn't seem that outlandish. Capuchins use stone tools. I'll repeat that: capuchins use stone tools. You mention chimp technology, and since we use tools - isn't it logical to assume tool manufacture was a trait of the LCA, therefore anything on the lines from the LCA to both chimps and humans had the capacity to make some sort of tool? Without tools and Isaac-approved butchery sites, the more interesting question remains the same: what happened around Gona's antiquity that made hominins start doing things differently than capuchins and chimps?

    Yeah, the bonus is never all that unlikely. I still think somebody will find a robust australopithecine in Asia.

    It's the mad persistence of Oldowan (and later Acheulean) that gets me. But then maybe it's not really so different from chimpanzees. Honey extraction, bushbaby spearing, and lots of other things are only at one or two field sites. But termite/ant fishing is everywhere. How do they keep that going? I suppose it's partly innate, or they have an innate bias toward learning it. Maybe Oldowan is like that, so there is a biological trigger supporting stone tools in later australopithecines.

  • Australopithecus afarensis used stone tools

    Wed, 2010-08-11 15:13 -- John Hawks

    UPDATE (2011-09-06) Note: The conclusions of the research were later critiqued, I posted on that criticism after this post.

    Shannon McPherron, Zeresenay Alemseged and colleagues working at the Dikika field site in Ethiopia have found evidence of stone tool use 3.39 million years ago [1]. That's 800,000 years earlier than the previous first-known tool use, and occurs during the existence of Australopithecus afarensis.

    The evidence is a series of cutmarks and one percussion mark on two bovid bones. One is a piece of rib from a large "cow-sized" animal, the other a femur fragment from a smaller "goat-sized" bovid. The analysis goes through several microscopic comparisons to rule out alternative causes for the cutmarks, such as trampling. The key paragraph of the results:

    The cut marks demonstrate hominin use of sharp-edged stone to remove flesh from the femur and rib. The location and density of the marks on the femur indicate that flesh was rather widely spread on the surface, although it is possible that there could have been isolated patches of flesh. The percussion marks on the femur demonstrate hominin use of a blunt stone to strike the bone, probably to gain access to the marrow. The external surfaces of ribs have thin sheaths of flesh, so the scraping marks on the fossil rib suggest stripping off of these sheaths.

    I have some lingering doubts, none of which are very serious, but that point out the need to look harder at other sites. It sure would have been nice if they'd found an anomalous sharp-edged rock nearby.

    The two bones are compelling, but the study does not give much indication of how representative they are. How many similar-sized bone fragments were left at the site? How many were collected? What fraction of "cutmarked" bones does that make? What fraction show signs of trampling and various kinds of post-depositional damage?

    Those questions are essential to answer the "green car" problem. If you don't know this one, it's fairly simple -- a witness reports a green car leaving the scene, and green cars are very rare -- the police think this is a great lead. But blue cars are very common in the city, and there is a small chance that the witness mistook a blue one for a green one. Whether it actually was a green car depends on the actual proportion of green to blue cars, and the actual probability that the witness was wrong.

    In this case, I think there is a very small chance that the marks on these bones could have been produced by processes other than deliberate cutting by a stone tool. But in a sample of hundreds or thousands of bone fragments, a small chance might well happen a couple of times. It's very difficult to quantify this, because archaeologists don't collect every bone fragment. The only real way to address the problem is to find more cutmarks and do other statistics on them -- do they occur where flesh is attached to bone, etc.

    It does seem odd that nobody's identified clear stone tools, which are in later sites a lot more common than cutmarked bones. A tool-user will make many artifacts during her life. (Why "her"? Well, in chimpanzees, it's the females who dominate technology transmission...) We have a lot of australopithecine bones. If this was a long-lasting tradition, we should have found a lot of stone tools by now.

    Maybe it wasn't a long-lasting tradition. Chimpanzee technology is significantly clustered geographically, some of the most interesting behaviors have been observed only at a single field site. If Australopithecus had a similar pattern of cultural diversity, tool use may have been innovated many times without "catching on" over a wide geographic or temporal extent. Here's what McPherron and colleagues conclude along similar lines:

    Whether A. afarensis also produced stone tools remains to be demonstrated, but the DIK-55 finds may fit with the view that stone tool production pre-dates the earliest known archaeological sites and was initially of low intensity (one-to-a-few flakes removed per nodule) and distributed in extremely low density scatters across the landscape such that its archaeological visibility is quite low (16).

    Or maybe we just haven't noticed. Fluvial contexts may have been bad places for Australopithecus to hang out. McPherron and colleagues allude to this explanation for the local absence of tools at Dikika:

    However, stone tool production and consequently archaeological accumulations are not expected at this locality given the sedimentary environment characterized by the palaeo-Awash River emptying into a nearby lake (3, 4). In this relatively low-energy depositional environment, clasts suitable for stone tool production are not present (few particles larger than fine gravel, 8 mm diameter). Within the exposed SH Member, the distance from DIK-55 to cobble-sized raw materials (>64 mm) is ~6 km (at Gorgore; Fig. 1). Thus, in this instance the absence of evidence for stone tool production in the immediate vicinity of the cut-marked bones may reflect landscape-level raw material constraints.

    The research article is accompanied by an essay by David Braun reviewing the find [2]. He stretches a bit, but I think the interpretations he suggests are worth airing. One -- why are there cutmarked bones 6 km from any good source of stone raw material?

    The meat and marrow of large animals must have been a valued resource, because McPherron et al. conclude that the tool users incurred the cost of transporting stones 6 kilometres from where they occurred naturally to the site where the butchery took place. Further costs that were associated with the consumption of carrion, and were apparently worth the risk, include exposure to parasites and competition with large carnivores.

    Two -- what about the "meat-brain" connection?

    This provides exciting evidence of how A. afarensis behaved. At one time, the species was considered to be a relatively primitive hominin, but this perception is being redefined. For example, it now seems that Lucy's kin had body proportions that were more similar to those of humans than of apes (6). Analyses of the hand of A. afarensis show that it had relatively short fingers that would allow the kind of fine-scale manipulation necessary for tool use (7). A recently discovered skeleton from the Woranso–Mille area of Ethiopia suggests that A. afarensis did not have the ape-like, 'funnel-shaped' thorax usually associated with a large digestive tract and low-quality diet (8). Perhaps the findings that these hominins used tools and had a carnivorous component to their diet should not have been so unexpected.

    A 2.6-million-year-old butchery tradition should already have refuted the hypothesis that meat-eating caused the expansion of brain size in Homo. But it was still possible to maintain that the initial Oldowan was insufficiently dedicated, or that the anatomical specializations (e.g., small guts) allowing brain expansion took time to develop, or that as-yet-undiscovered large-brained hominins would be found. Any of these are still possible, but the observations Braun points out pretty much demolish the 15-year-old story of "expensive tissue." Australopithecus seems to have had a small gut, and a bigger brain than chimpanzees. If there was a tradeoff, A. afarensis had already made it.

    Braun didn't mention A. sediba, which adds another wrinkle. A late species of Australopithecus with human-sized teeth. Or (as some prefer), a pre-habilis species of Homo with an Australopithecus-sized brain. What was its diet like? I have a feeling we'll know before too long.

    Meanwhile, I'll be floating for the rest of the year, since I included this as the far-out "bonus" entry in my 2010 New Year predictions! You know, the one that's so bizarre that it seems like it'll never happen. Heh.

    UPDATE (2010-08-11): John Noble Wilford got ahold of some skeptics for his NY Times story on the discovery:

    Still, the discoverers are already being pressed to defend their interpretation that the cut marks on the bones are evidence of stone-tool butchery. Tim D. White of the University of California, Berkeley, one of the foremost investigators of early human origins, said flatly that their “claims greatly outstrip the evidence,” and noted, “We have been working sites in this area for 40 years, and not a single stone tool has been found in deposits of this antiquity.”

    Sileshi Semaw, a paleoanthropologist at Indiana University who was a discoverer of the oldest confirmed stone tools, from 2.6 million years ago, noted in an e-mail message from Ethiopia that researchers had often been misled by bone markings left by trampling animals and other natural causes. “I am not convinced of the new discovery,” he said.

    UPDATE (2010-08-12): Maybe some are looking for more about australopithecine diets. My post from 2005, "Chemistry and early hominid diets" has a good compilation of stable isotope observations and what may explain them. With the cutmark evidence, you can read through the discussion of C4 plant contributions, and think about the grazers that A. africanus may have been eating.

    UPDATE (2010-08-16): Science Friday with Ira Flatow covered this story last week, including commentary by Alemseged and David DeGusta, who suggests that the marks may be crocodile bite marks. Doesn't look like it to me, but as I wrote above, I'd like to see statistics on a few hundred damaged bones to see the probability that an arbitrary one will look like stone cutmarks.


    References

    Synopsis: 
    A report finds cutmarks on fauna from Dikika, Ethiopia, 3.4 million years ago.
  • Fishy story from Koobi Fora

    Sun, 2010-06-13 08:30 -- John Hawks

    I have to credit a reader for that headline, and for forwarding the paper. It's another case of the infamous PNAS release policy. The press that came from the paper's announcement preceded the paper's availability in this case by a week. That approaches the case where a Hollywood studio won't screen a movie for reviewers before it's released. That means no reviews, which in the case of movies can only mean one thing. It's bad.

    Scientific papers fortunately don't suffer from this shortfall -- the quality of the paper seems more or less unrelated to the release policy of the journal. In this case, the press went with a story that is interesting, but not necessarily that important in the scheme of things. And I don't get to write about it until two weeks after the news stories hit the presses.

    David Braun and colleagues report on the fauna at locality FwJj20 of Koobi Fora, Kenya. The archaeological remains here, including stone tools and fauna, date back to 1.95 million years. It's an interesting time because of what may have been going on with hominin anatomical evolution, but does it represent anything new in behavioral evolution?

    The authors point out that there are archaeological sites that are much older, going back to 2.6 million years. Some of those earlier localities -- notably, the earliest, Gona OGS 6 and OGS 7 localities -- have hundreds of stone artifacts combined with fauna and hominin-modified bones. FwJj20 stands out in combining a very large number of stone artifacts (2633) with a high proportion of hominin-modified bones (5.9 percent of 405 faunal specimens). Even in later deposits such as Olduvai Gorge that have a high number of localities with some stone tools, it is rare to find localities with evidence of butchery of many animals. Those are the kinds of archaeological debris that would be expected of a real focus of hominin behavior. So every additional site like this adds substantially to our knowledge of hominin behavior at the dawn of hunting and gathering.

    Here, one interesting aspect of the faunal exploitation is the small amount of surface modification consistent with bone-smashing. The authors suggest that the site had little marrow extraction than expected based on experimental replication of butchery. There is very little evidence for carnivore activity at the site, and both bones and faunal remains are clustered within a small vertical horizon of around 6 inches in thickness. The presence of small flakes and bone fragments helps to substantiate that the site did not accumulate under the influence of high-velocity water flow, and that it represents a primary activity locus for the hominins who left the tools there.

    The faunal assemblage is interesting for the relatively high proportion of aquatic animals preserved, including both turtle and crocodile bone specimens with cut marks, and some fish bones. This is the part of the paper emphasized in the press that described the site, and the paper gives a good summary of the aquatic proportion of the fauna, including the evidence that the animals were actually butchered by the hominins.

    The skeletal representation of fish bones [over-abundance of cranial fragments: 64% of fish NISP (28)] and turtle/tortoise bones [over-abundance of carapace and plastron fragments: 90% of turtle/tortoise NISP (29)] corresponds to ethnographic and archaeological distributions associated with hominin foraging. The number and taxonomic diversity of hominin-modified bones imply that hominins used the FwJj20 locality for the acquisition of meat from several different carcasses of terrestrial and aquatic animals as well as marrow from mammalian bones. This provides strong evidence of a diverse animal component in the diets of hominins before the appearance of H. ergaster/erectus (Braun et al. 2010:10004).

    But....I think that the relevance of the aquatic animals has been exaggerated. According to the MNI (minimum number of individuals) table in the paper, the turtle and crocodile bones may represent one single turtle and one crocodile. The number of fish bones is also very small -- only 15 total, and the authors do not provide an MNI for fish. Compare these small numbers to a minimum of 11 hippopotamus individuals represented by in situ bone elements, and 17 bovids. One turtle. Seventeen bovids.

    MNI is not the best indicator of dietary importance -- for mammals, it is heavily influenced by mandibles and teeth. Humans may drag mandibles back to a central place as part of the head, even if they eat the rest of the animal elsewhere. Being highly diagnostic, we can work out easily when there were lots of individuals from a mandible -- not so for broken turtle carapace pieces. But it's not very meaningful to count every crocodile bone, either. The site really does not provide any evidence that reptiles and fish simply made up a large fraction of the meat consumed there.

    From my perspective, I think that's just fine. Aquatic animals aren't important because of their sheer numbers, but because they tell us about the flexibility of foraging behavior. Living hunter-gatherers eat turtles and reptiles when they can, and because they are usually small food packages, they often eat them where they find them instead of returning to a base camp first. Hunter-gatherers are flexible in what they eat and where they eat it. FwJj20 is showing at least a substantial taxonomic flexibility in the meat-eating of early Oldowan hunters.

    Croc, turtle and fish remains also document that the Oldowan-makers were actively foraging in and around river or lake margins. That may not be earth-shaking, since we are, after all, talking about a water-dependent primate in a hot climate. But sometimes the importance of an archaeological discovery is that it strikes a "couldn't have done it" from the record.

    Still, this really isn't a case where anybody could credibly maintain that early hominins were excluded from foraging on lake or river margins. Just last year I discussed two archaeological sites that give evidence for human exploitation of aquatic resources in the Early and Middle Pleistocene. At Trinil, Java, it seems clear that people were exploiting molluscs ("The shells of Trinil"), and the somewhat later Gesher Benot Ya'aqov site in Israel has evidence of systematic fish and crab exploitation ("The fishy spaces of the Middle Pleistocene"). The possible exploitation of papyrus by A. boisei also would show a mastery of shoreline habitats by hominins. It's hard to argue that the threat of the water was lower for robust australopithecines than for Homo.

    Finding such repeated evidence of aquatic resource use, extending back near the dawn of stone tool manufacture, ought to prove one thing: The fatty acids in aquatic meat were not the cause of the expansion of brain size in Homo erectus.

    Oh, I know, the news stories all said exactly the opposite, claiming that the fatty acids were essential to brain growth, and that this shows that stone tools were important to getting this essential nutrient. Hey, Braun and colleagues started it -- they wrote it right in the last sentences of the paper:

    In addition, although animal tissues provide nutrient-rich fuel for a growing brain, aquatic resources (e.g., fish, crocodiles, turtles) are especially rich sources of the long-chain polyunsaturated fatty acids and docosahexaenoic acid that are so critical to human brain growth (2). Therefore, the incorporation of diverse animals, especially those in the lacustrine food chain, provided critical nutritional components to the diets of hominins before the appearance of H. ergaster/erectus that could have fueled the evolution of larger brains in late Pliocene hominins (Braun et al. 2010:10005).

    But "fueled" is a metaphor, not a valid evolutionary concept.

    I accept that reptile and fish meat may be nutritionally desirable. The question is whether they caused the increase in brain size associated with Homo. One way to read that hypothesis is as Lamarckism, which is simply wrong (Larry Moran has commented on that topic). I don't think that any paleoanthropologists are seriously Lamarckist, but some need to be more careful how they describe the relationship of fitness and diet.

    Let me construct a version of the hypothesis consistent with evolutionary biology. Suppose that other factors -- social competition, technological requirements -- induced selection for cognitive skills in early Homo. The response of the population to this selection may have been impeded by selection in favor of smaller brains and/or shorter life histories. That is to say, directional selection on cognition may have been impossible because of stabilizing selection on brain growth. Now diet changes might become relevant, by relaxing the stabilizing selection on brain growth. This scenario might predict an increase in the size of the brain when people began to consistently supply themselves or their children with the right nutrition.

    Understand that I don't subscribe to this hypothesis. We have much to learn about what the "right" nutrition might be.

    But the hypothesis is testable. The archaeology now suggests that significant meat consumption preceded the expansion of the brain by a half million years or more, and that fish and reptile meat made up a hunter-gatherer-like part of early hominin meat consumption from the start.

    Now it could be that later increases in diet quality -- for example, by increasing the total amount of meat, or decreasing nutritional unpredictability -- are what actually caused (or allowed directional selection on) the increase in brain size. That change would be a different hypothesis, however -- the hypothesis that selection against larger brains was relaxed by behavioral innovation. Fish fat could be a correlate of behavioral change in this hypothesiss, but it would not be the cause.

    References:

    Braun DR, Harris JWK, Levin NE, McCoy JT, Herries AIR, Bamford MK, Bishop LC, Richmond BG, Kibunjia M. 2010. Early hominin diet included diverse terrestrial and aquatic animals 1.95 Ma in East Turkana, Kenya. Proc Nat Acad Sci USA 107:10002-10007. doi:10.1073/pnas.1002181107

    Synopsis: 
    The Turkana Basin joins other areas providing evidence of dietary flexibility and aquatic resource use by early Homo.
  • Earlier arrival of stone tools on Flores

    Thu, 2010-03-18 09:56 -- John Hawks

    A new paper is pushing back the time of initial occupation of Flores by hominins to at least 1.0 million years ago. Adam Brumm and colleagues (2010) are reporting that they've found stone tools in a site from the Soa Basin of Flores, the same geological region as the previous site of Mata Menge.

    The Wolo Sege excavation yielded no faunal remains, but 45 in situ stone artefacts were recovered from the conglomerate and two fine-grained metavolcanic flakes were excavated from the lower tuffaceous siltstone layer ~15–20 cm above the Ola Kile Formation (Fig. 3e, f). A single volcanic flake was also recovered from the upper overbank deposit during extraction of sediment for dating. The Wolo Sege stone artefacts are predominantly small and morphologically undifferentiated flakes struck from cobbles by direct hard-hammer percussion (Fig. 3; see also Supplementary Fig. 2), but include a bifacially and centripetally worked ‘radial’ core, similar to those characteristic of the Mata Menge assemblage of stone artefacts.

    The radial core is not illustrated, but several of the flakes are figured in the paper. The conglomerate in question is overlain by a layer with a minimum date of 1.02 million years.

    A date of 880,000 years ago for human occupation made for a convenient explanation of faunal turnover on the island, which happened around that time. The turnover included the extinction of the small pygmy stegodont species Stegodon sondaari, which was replaced in later faunal assemblages by the Java-derived Stegodon florensis. It also included the extinction of giant tortoises.

    This suggests that the non-selective, mass death of S. sondaari and giant tortoise, associated with stratigraphic evidence for a major volcanic eruption at Tangi Talo ~0.9 Myr ago10, could represent a localized or regional extinction, and that the faunal turnover may have been a result of climate change, volcanic activity or some other natural process or event (Fig. 5).

    I discussed this with my graduate seminar yesterday. The long persistence of this toolmaking culture, in what must have been a rather small human population, is weighing on my mind. Were there recurrent contacts from Java, keeping the population going? How dependent were these people on their tools?

    Hominin predators can lead to unstable dynamics -- most predators will undergo predator-prey cycles, but humans can switch to other resources and continue to press a small prey species to extinction. The long persistence of tasty animals on Flores in the presence of hominins suggests that the subsistence practices of these hominins were different in some ways from later humans.

    This finding doesn't really help us to resolve the issues of the later Flores record, including the relationships of the skeletal individuals with other hominins. There's been some press about the hobbits lately, but it's all paleoanthropological tree-marking -- except for the news that they'll be reopening excavations at Liang Bua.

    References:

    Brumm A, Jensen GM, van den Bergh GD, Morwood MJ, Kurniawan I, Aziz F, Storey M. 2010. Hominins on Flores, Indonesia, by one million years ago. Nature (advance online) doi:10.1038/nature08844

  • The spotty Acheulean

    Wed, 2009-09-02 22:59 -- John Hawks

    Scott and Gibert report in today's Nature on the "oldest handaxes" in Europe:

    In Africa, large cutting tools (hand-axes and bifacial chopping tools) became part of Palaeolithic technology during the Early Pleistocene (1.5 Myr ago). However, in Europe this change had not been documented until the Middle Pleistocene (

    The "Anthro 101" version of the Acheulean makes it out to be a million-year-long technological yawn. The breakthrough of the first handaxes 1.5 million years ago led to a stultifying stasis. The handaxe was a "Paleolithic pocket knife" useful for many purposes -- but the advent of Levallois manufacture around 300,000 years ago consigned the handaxe to the midden of history. Except, of course, for scattered, benighted peoples who were still using handaxes up into historic times -- the exceptions proving the rule of bifaces' never-ending utility.

    Well, the Acheulean was boring, but it wasn't uniform. The Anthro 101 version makes Acheulean people sound too accomplished -- like they invented the bifaces and then started turning them out like industrial robots for a million years.

    Not so: Fine, finished bifaces tend to be less than 500,000 years old. They also tend to be European. Acheulean people didn't usually carry rock very far. With more sources of chert and flint, Europe's geology allowed a wider selection of fine handaxes than Africa's. That is, at least after 500,000 years ago or so. Before then, there just weren't very many handaxes in Europe.

    Here, Scott and Gibert suggest that maybe some other sites with "advanced" or "terminal" Acheulean may prove to be earlier than people now think. The two sites in this study were both initially thought to be much later -- for example:

    The youthful age (200 kyr old) assumed for Solana del Zamborino was largely based on its well-developed Acheulian lithic typology. Such a young age contrasts with our continuing lithostratigraphy and palaeoclimate research in the region, which indicates a final, major lake-forming event near the end of the Early Pleistocene (starting 800 kyr ago) and deposition terminating in the Baza Basin (600 kyr ago).

    They could well be right -- some European sites now thought to be late (post-500 kyr) might be earlier. What does that mean for our understanding of the Acheulean?

    Lower Pleistocene Europeans sometimes made finished bifaces, these were initially sporadic, and later became more and more common until the advent of Middle Paleolithic technocomplexes. The sporadic appearance suggests that people could live without handaxes, and that they were simple enough to be repeatedly invented. There's just not that much information content there, and groups of Early to Middle Pleistocene people arrived at the same solutions again and again.

    Technological "progress" is a misnomer before around 300,000 years ago. Early Homo made Oldowan (and Oldowan-like) industries that required few capabilities not mastered routinely by wild chimpanzees. Some, sure, but few. Bifaces require a bit more: a spatial conception of symmetry, longer action sequences. But Early and Middle Pleistocene people didn't carry it off all the time; they kept losing the biface outside Africa. And they kept hitting that biface mode. Curious.

    Other entries of interest:

    "Early Malaysian axes

    And then there was Levallois

    How monolithic was the Acheulean?

    Acheulean endings

    References:

    Scott GR, Gibert S. 2009. The oldest hand-axes in Europe. Nature 461:82-85. doi:10.1038/nature08214

  • Handedness in ancient hominins

    Mon, 2009-08-31 08:30 -- John Hawks

    Michael Balter writes about the work of Liverpool archaeologist Natalie Uomini, who is studying the evolution of handedness by experiment and attempting to find signs of hand dominance in finished stone tools.

    Uomini argues that these findings [in human experiments] are similar to those found in studies of nonhuman primates, in which the degree of handedness varies depending on the complexity of the task they are facing and the level of skill required to perform it. The nut-cracking task required five basic actions, Uomini says—“grasp nut, place nut on anvil, grasp hammer, hit nut, and eat nut”—whereas the puzzle required at most three actions (grasp flake, grasp core, fit flake to core.) And along with other researchers who have offered a similar hypothesis, she suggests that the increasing sophistication of hominin toolmaking technologies over time may have selected for a greater degree of handedness. Indeed, Uomini says, the “technology-dense lifestyles” of early hominins might have required our ancestors to more or less make up their minds about what hands they were going to use to perform complex tasks. Moreover, such hand bias could have aided the learning process as hominins taught each other toolmaking and other skills; a number of studies have shown that people learn manually difficult tasks, such as knot-tying, more easily when they use the same left- and right-hand movements as their teachers.

    In other words, once a procedure becomes sufficiently complex, it is likely to require asymmetric spatial operations that will be learned in a biased way from models who have mastered the procedure. But if a model bias is likely to exist, that's not sufficient to induce selection in favor of added bias. Random changes that reinforced the bias wouldn't be selected against, but that still leaves us wanting an explanation for the frequency of lefties -- as Balter and Uomini both point out.

    I'm not sure that this technological explanation actually explains anything. Possibly the causation is in the opposite direction: right versus left handedness tends toward a given frequency for other reasons (maybe pleiotropy, maybe chance) and the use of hands in technology accommodates to the prevailing population mean -- to a greater or lesser extent for more or less complex procedural operations.

    Still, it's a very interesting article about some clever ways of applying behavioral science in archaeology.

  • Plant processing with early Oldowan tools

    Tue, 2009-05-05 00:24 -- John Hawks

    Ann Gibbons was at the AAPA meetings early last month, and she reports in the current Science on some of the research. Her article about the use of early Oldowan tools from Kanjera, Kenya focuses on the evidence for plant processing:

    To find out just what early Homo was doing with the tools, [archaeologist Thomas] Plummer enlisted archaeologist Cristina Lemorini of the University of Rome, "La Sapienza." She studied replicas of the Kanjera tools, made with the same kinds of stone, that modern Hadza hunter-gatherers of Tanzania had used to butcher animals, process wild tubers, cut grass, and work wood. Then, using confocal and metallographic microscopes, she compared patterns of wear on the edges of the Kanjera tools with those on the replicas. She reported that the ancient tools had telltale signs of being used to process plant materials, such as cutting grass, and the distinct striations made by sediment as tools were used to clean and section fibrous tubers. She also saw patterns consistent with defleshing carcasses and woodworking, possibly to make wooden tools.

    Kanjera has been the subject of some very interesting raw material analyses over the last couple of years, by David Braun and colleagues (2008, 2009), documenting the selectivity of the Oldowan-makers for particular kinds of raw materials -- studies that have counterparts at other early Oldowan sites, including Lokalalei (Harmand 2009).

    Meanwhile, the analysis of use-wear and plant residues on stone tools has advanced markedly in the last ten years. Use-wear analysis considers the kind of microwear produced on artifacts by repeated use against materials like wood, hide, meat, and bone. For many years, archaeologists have worked on microwear -- for example, Lawrence Keeley and Nick Toth (1981) showed that wear patterns on the edges of Oldowan tools from Koobi Fora are consistent with use in both meat and plant processing. But use-wear analysis has undergone recurrent debate over the years, as people questioned the qualitative assessments of similarity between reference tools -- used by experimenters on known materials -- and archaeological artifacts. A short review of this history is given by Evans and Donahue (2008).

    A certain ambiguity about use-wear studies remains unresolved -- how much of the results are in the eye of the analyst? It helps a lot to have additional evidence. Plant residues and phytoliths have increasingly provided such evidence -- the actual parts of plants adhering to stone tools with use-wear that looks like plant materials makes it look pretty likely that the tools were used on the plants. To list some highlights, we have:

    1. Nuts and nutcracking at Gesher Benot Ya`aqov (Goren-Inbar et al. 2002).

    2. Woodworking, as documented by phytoliths and plant fibers adhering to initial Acheulean tools from Peninj (Dominguez-Rodrigo et al. 2001).

    3. Starch grains also can adhere to stone tools, and starch processing is clear in the Middle Stone Age of Mozambique (Mercader et al. 2008).

    4. A range of starchy and woody plant materials were processed by Mousterian (presumably Neandertal) people from Starosele and later Upper Paleolithic people from Buran Kaya III -- similar between the two sites despite their difference in time (Hardy et al. 2001). Some tools had both mammalian hair and feather barbules attached.

    There's an endless range of such studies; a deep literature, so that a few highlights don't really do it justice. A few studies, like the last one here, actually consider enough artifacts to start to develop an idea of the activity patterns of people. When you're only studying three or four artifacts that preserve any microwear, you've got evidence that a few things did happen sometimes, but you really don't have a full pattern.

    References:

    Braun DR, Plummer T, Ditchfield P, Ferraro JV, Maina D, Bishop LC, Potts R. 2008. Oldowan behavior and raw material transport: perspectives from the Kanjera Formation. J Archaeol Sci 35:2329-2345. doi:10.1016/j.jas.2008.03.004

    Dominguez-Rodrigo M, Serrallonga J, Juan-Tresserras J, Alcala L, Luque L. 2001. Woodworking activities by early humans: a plant residue analysis on Acheulian stone tools from Peninj (Tanzania). J Hum Evol 40:289-299. doi:10.1006/jhev.2000.0466

    Evans AA, Donahue RE. 2008. Laser scanning confocal microscopy: a potential technique for
    the study of lithic microwear. J Archaeol Sci 35:2223-2230. doi:10.1016/j.jas.2008.02.006

    Gibbons A. 2009. Of tools and tubers. Science 324:588-589. doi:10.1126/science.324_588b

    Goren-Inbar N, Sharon G, Melamed Y, Kislev M. 2002. Nuts, nut cracking, and pitted stones at Gesher Benot Ya`aqov, Israel. Proc Nat Acad Sci USA 99:2455-2460. doi:10.1073/pnas.032570499

    Hardy BL, Kay M, Marks AE, Monigal K. 2001. Stone tool function at the paleolithic sites of Starosele and Buran Kaya III, Crimea: Behavioral implications. Proc Nat Acad Sci USA 98:10972-10977. doi:10.1073/pnas.191384498

    Harmand S. 2009. Variability in Raw Material Selectivity at the Late Pliocene sites of Lokalalei, West Turkana, Kenya. Pp. 85-97 in Hovers E, Braun DR, Interdisciplinary Approaches to the Oldowan. Springer, Amsterdam. Amazon

    Keeley LH, Toth N, 1981. Microwear polishes on early stone tools from Koobi-Fora, Kenya. Nature 293:464-465.

    Mercader J, Bennett T, Raja M. 2008. Middle Stone Age starch acquisition in the Niassa Rift, Mozambique. Quatern Res 70:283-300. doi:10.1016/j.yqres.2008.04.010

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