john hawks weblog

paleoanthropology, genetics and evolution

Neandertals

  • Neandertal night on PBS

    Tue, 2013-05-14 09:34 -- John Hawks

    This Wednesday (May 15) is Neandertal night on PBS stations in the U.S., with two documentary programs covering the last few years of science about these ancient people.

    First, the NOVA episode this week is the "Decoding Neandertals" program. This was broadcast earlier this year, and it is a really good summary of some current research into Neandertal genetics and behavior:

    Over 60,000 years ago, the first modern humans—people physically identical to us today—left their African homeland and entered Europe, then a bleak and inhospitable continent in the grip of the Ice Age. But when they arrived, they were not alone: the stocky, powerfully built Neanderthals had already been living there for hundred of thousands of years. So what happened when the first modern humans encountered the Neanderthals? Did we make love or war? That question has tantalized generations of scholars and seized the popular imagination. Then, in 2010, a team led by geneticist Svante Paabo announced stunning news. Not only had they reconstructed much of the Neanderthal genome—an extraordinary technical feat that would have seemed impossible only a decade ago—but their analysis showed that "we" modern humans had interbred with Neanderthals, leaving a small but consistent signature of Neanderthal genes behind in everyone outside Africa today. In "Decoding Neanderthals," NOVA explores the implications of this exciting discovery. In the traditional view, Neanderthals differed from "us" in behavior and capabilities as well as anatomy. But were they really mentally inferior, as inexpressive and clumsy as the cartoon caveman they inspired? NOVA explores a range of intriguing new evidence for Neanderthal self-expression and language, all pointing to the fact that we may have seriously underestimated our mysterious, long-vanished human cousins.

    Second, a new episode of Secrets of the Dead is being broadcast, titled "Caveman Cold Case", about El Sidron Cave:

    A tomb of 49,000 year-old Neanderthal bones discovered in El Sidron, a remote, mountainous region of Northern Spain, leads to a compelling investigation to solve a double mystery: How did this group of Neanderthals die? And, could the fate of this group help explain Neanderthal extinction? Scientists examine the bones—buried over 65 feet below ground—and discover signs that tell a shocking story of how this group of six adults, three teenagers, two children and a baby may have met their death. Some bones have deep cuts, long bones are cracked and skulls crushed—distinct signs of cannibalism. Was it a result of ritual or hunger? Neanderthal experts are adamant that they were not bloodthirsty brutes. Will this investigation challenge their views? What happened here 49000 years ago will take us on a much bigger journey—from El Sidron to the other end of the Iberian Peninsula where scientists are excavating beneath the seas off Gibraltar in search of Neanderthal sites. Scientists working here had theories—but no proof—for why Neanderthals went extinct. El Sidron may change this.

    I'm really excited that this one is being broadcast in the U.S. -- it covers the science from a forensic point of view, including new insights about diet and breadth of behavior. It is a great program that goes into the research by Antonio Rosas and Carles Lalueza-Fox on the Spanish Neandertals, and gives us a viewpoint on the Gibraltar Neandertals with Clive Finlayson.

    I play a small part in both programs, and I'm happy to see the Neandertals getting such high-profile attention!

  • 180 million Neandertals

    Tue, 2013-04-16 14:58 -- John Hawks

    Just got back proofs of a book chapter I have coming out soon with Zach Throckmorton. My favorite paragraph:

    Nearly seven billion people inhabit our planet. At least six billion carry the genes of Neandertal ancestors. Inheritance from Neandertals makes up approximately 3% of the genomes of randomly chosen people outside sub-Saharan Africa today (Green et al., 2010; Reich et al., 2010). A back-of-the-envelope calculation shows if we took all of the Neandertal genes from today’s human population, we would have enough raw material to make up 180 million Neandertals.

    I love that because it makes the Neandertals into the evolutionary success story they really were. They succeeded by becoming part of us.

    UPDATE (2013-04-18): You can tell from this excerpt how long edited book chapters can take to come out, as we've been more than seven billion for quite some time now! That's one of the changes we'll be making to the galleys.

  • Riparo Mezzena and the Neandertal transition

    Sun, 2013-03-31 00:38 -- John Hawks

    A paper by Silvana Condemi and colleagues examines the anatomy of a partial mandible from Riparo Mezzena, Italy [1]. The mandible is a relatively late Neandertal specimen by its archaeological association and mtDNA sequence. As the introduction to the paper notes, the identities of skeletal specimens in the timespan from 45,000 to 30,000 years ago across Europe have been shifting along with radiocarbon ages and further analyses of fragmentary specimens. In this case, like other late Neandertals, the specimen bears a chin:

    This study of the Mezzena mandible shows that the chin region is similar to that of other late Neanderthals which display a much more modern morphology with an incipient mental trigone (e.g. Spy 1, Saint Césaire). In our view, this change in morphology among late Neanderthals reopens the debate on the "more modern like" morphology of late Neanderthals and can lend support to the hypothesis of a certain degree of continuity with AMHs or a possible interbreeding with them.

    The paper concludes that the Mezzena mandible lies morphologically amid the sample of modern humans from Upper Paleolithic and Levantine Middle Paleolithic contexts, even when compared to Neandertals like Saint Césaire or La Ferrassie 1 that have relatively vertical mandibular symphyses.

    I prefer not to play the game, "is it a Neandertal?", "is it a modern human?" If we had a sample of well-dated relatively complete specimens across the period from 45,000 to 30,000 years ago, we could test the hypothesis that two populations (earlier Neandertals and later "modern" humans) were genetically well-differentiated from each other. We don't have that sample.

    In my view, we shouldn't assume more than we know, which is that both the frequencies and combination of traits of earlier Neandertals are much more strongly present in Mousterian-associated specimens than in other, mostly later, industries. I don't yet see a reason to exclude the hypothesis that this pattern reflects both evolution and migration into Europe. And as I wrote last year, the late Neandertals may represent both evolution and migration into Europe from a central Asian or West Asian source population [2].

    One effect of genetic sequences has been to demonstrate that anthropologists' morphological distinctions among Neandertals don't match the groupings we would make along purely genetic lines. I considered this problem in my paper last year, "Dynamics of genetic and morphological variability within Neandertals" (open access, PDF) [2]. Jim Ahern and colleagues (including me) have showed that the Vindija G3 Neandertals have morphological features that are not typical of classic Neandertals, and that are significantly different in the modern human direction [3], [4]. Here's what I wrote last year:

    The discussion of genetic diversity among these Neandertals has not yet attempted to reconcile their genealogical arrangement with morphological classification schemes. The later Western European Neandertals that share a close mtDNA genealogical connection (Vindija-Feldhofer-El Sidrón) are not synonymous with "classic Neandertals". The well-known classic Neandertals include specimens such as La Chapelle-aux-Saints (France), La Ferrassie 1, Monte Circeo 1 (Guattari) as well as Feldhofer 1. This classic Neandertal sample includes specimens earlier than 70,000 years old and some as recent as 45,000 years ago. The classic Neandertals flank both the earlier and later sides of the 50,000-year-ago dispersal of Neandertals proposed by Dalen and colleagues (Dalen et al., 2012).

    Meanwhile, the clade that connects late European Neandertal mtDNA into a tight cluster includes great morphological diversity. The two Vindija mtDNA sequences included by Dalén and colleagues (Dalen et al., 2012) are both from layer G3 of the site, perhaps 40,000 years old. Both are derived from postcranial fragments without diagnostic morphological traits. The other material from G3 includes cranial, mandibular and dental remains that are not synonymous with classic Neandertal morphology (Ahern, 2004). These late Neandertals from Vindija display less pronounced morphology than classic Neandertals and lack traits that are common in the earlier classic Neandertals (Smith, 1992). These specimens are connected to Feldhofer and El Sidrón not only by mtDNA relationships but also their very low nuclear DNA diversification. If the Vindija specimens can be lumped together in mtDNA and nuclear DNA diversity with the remains from El Sidrón and Feldhofer, it seems possible that traditional morphological groupings will fail to capture real biological differences among Neandertal populations.

    Riparo Mezzena adds further to this pattern. I would note that this looks at the moment like the specimen most likely to give rise to an Italian Neandertal whole genome. As we begin to examine the data from the Denisova Neandertal specimen ("A new high-coverage Neandertal genome"), the population genetics of later Neandertals will come more and more into focus.

    Steven Churchill and Fred Smith wrote a review of the initial Upper Paleolithic skeletal record several years ago [5] that still remains the best single summary of the remains from this time period. What strikes you in this review is the overall fragmentary nature of the record. That review is already out of date in some respects, as a number of specimens have been moved into or out of this period by radiocarbon revisions, and the archaeological conception of "early Aurignacian" has substantially changed.

    There really ought to be an equivalent review for the latest Neandertals. I think that the sample has become more complex and confusing as we have developed a better idea of the genetics.


    References

    Synopsis: 
    Morphological comparisons of a late Neandertal reinforce the hypothesis of population mixture in Europe.
  • A new high-coverage Neandertal genome

    Wed, 2013-03-20 00:32 -- John Hawks

    Today, Svante Pääbo's group at the Max Planck Institute for Evolutionary Anthropology released high-coverage sequence data from a toe bone from Denisova Cave. The new genome comes a year after the same group released the high-coverage genome of the Denisova finger bone, several months before they published the first high-coverage analysis of this ancient genome [1]. Today's announcement is here: "A high-quality Neandertal genome sequence". It adds a second high-coverage genome from Denisova Cave, this one from a toe bone. Unlike the first finger bone genome, this toe has produced a genome very much like Neandertal specimens from much further west, including the Vindija Neandertals.

    Something interesting in these data: the presence of a Y chromosome.

    There's not so terribly much we can say about a toe. This particular bone was first reported in 2011 by Mednikova [2], who described the specimen's anatomy. She found the toe similar in some respects to equivalent Neandertal toe bones, but also like recent humans in a couple of details. Still, the anatomy wouldn't be enough to conclude that the bone is a Neandertal, because we don't know much about the toes of other ancient human populations.

    The genetics are fairly clear about the level of similarity of this new genome to other Neandertals. From the announcement:

    Similarity of Neandertals and Denisova genomes

    The figure shows a tree relating this genome to the genomes of Neandertals from Croatia, from Germany and from the Caucasus as well as the Denisovan genome recovered from a finger bone excavated at Denisova Cave. It shows that this individual is closely related to these other Neandertals. Thus, both Neandertals and Denisovans have inhabited this cave in southern Siberia, presumably at different times.

    This is a cluster diagram based on genome-wide similarity, which doesn't tell us about possible mixture among the populations. But it does show the high degree of similarity among the known Neandertals. This new specimen from Denisova (labeled "Altai") is a bit further from them than they are to each other, but not much. It will be interesting to assess this degree of similarity in comparison with the within-population similarity of more living human populations.

    I'm reluctant to accept a dichotomy of "Denisovan" versus "Neandertal". Distinguishing the samples in that way invites a typological assumption about the ancient people, giving an impression of distinctness that I'm not yet convinced about. It remains to seriously investigate the hypothesis that one or both of these putative samples represents some amount of gene flow from each other, or from yet more ancient populations. But I suppose we're stuck with the "Neandertal from Denisova" and the "Denisovan from Denisova".

    Unless we go for "manual genome" versus "pedal genome", which is admittedly unappealing.

    There's not much meat in this announcement, that will wait for the full published analysis that we can expect later this year. The most important aspect of this, like the Denisova data availability from last year, is that we can now start working with the high-quality data. As someone who works with sequences, I cannot overstate the importance of having the best high-coverage data available for our work.

    I have a paper in preparation where I make a relevant analogy, in this case noting last year's high-coverage Denisovan genome in comparison to the history of ancient DNA sequencing:

    To put this into context: the original 360bp sequence from Feldhofer 1 has been memorialized on a cross-shaped plaque at the site outside Mettmann, Germany. This plaque is approximately 1 square meter in size. A similar monument to contain the Denisova high-coverage data would need to be more than 14 kilometers across. Compared to the first sequencing effort in 1997, today’s state of the art involves the generation of more than 200 million times more data.

    It's a pretty awesome time for those of us exploring human evolution!


    References

    Synopsis: 
    Noting the announcement of new data availability from Denisova
  • Speaking of Neandertal FOXP2

    Tue, 2013-01-29 00:39 -- John Hawks

    Tomislav Maricic and colleagues from Svante Pääbo's group have reported finding a regulatory change in the gene FOXP2 that may be of relevance to the evolution of human speech [1]. To telegraph the conclusion, the paper does not demonstrate that Neandertals or Denisovans were different from humans in speech or language-relevant phenotypes.

    Most important, a substantial number of living people share the ancestral genotype inferred for Neandertals and Denisovans for the site considered in the study. It is a genetic change within living people that may have been important, but it is an instance where human variation includes the Neandertal genotype.

    I'm going to let the paper's mini-review do the work of describing the background to the study:

    Among humans, sequence variation around exon 7 shows an excess of derived nucleotide variants at high frequencies and of rare nucleotide variants, indicating that the region has been affected by a selective sweep (Enard et al. 2002; Zhang et al. 2002; Yu et al. 2009). It has been estimated that this happened within the last 200,000 years (Enard et al. 2002) or 55,000 years (Coop et al. 2008). Because it was initially assumed that at least one of the two amino acid substitutions were the cause of the sweep, it was expected that at least one of them would not be present in Neandertals, who shared a common ancestor with modern humans 370–450,000 years ago (Green et al. 2010). However, both nucleotide substitutions were found in two Neandertals from Spain (Krause et al. 2007) as well as in Neandertals from Croatia (Green et al. 2010), and in Denisovans, an extinct Asian hominin group related to Neandertals (Reich et al. 2010). Furthermore, it was found that linkage disequilibrium extends across exon 7 in present-day humans, which is not expected if one of the two amino acid changes in exon 7 was the target of selection (Ptak et al. 2009). Hence, although at least one of the two amino acid changes is very likely evolutionarily relevant given the functional data and the conservation of FOXP2, they are not likely to be the cause for the selective sweep. Assuming that a sweep did occur, it must therefore be caused by some other variant in the region, possibly affecting the regulation or splicing of FOXP2.

    It was a big story that humans had a recent sweep in this gene, eliminating most of the variation, and that humans are different from other primates in the coding sequence. But the apparent timing of the sweep did not make sense in combination with the observation that Neandertals share the human coding sequence.

    One resolution of these observations is the hypothesis that the human version of FOXP2 simply came from Neandertals. I wrote about a short paper by Graham Coop and colleagues in 2008 that went along similar lines ("FOXP2 is really recent, it really did introgress (if it's not contamination)"). Coop and colleagues substantiated the hypothesis of a recent selective sweep, but at the same time they did acknowledge that selection on some other linked locus might account for the evidence.

    Maricic and colleagues have found another linked genetic change that could account for the sweep. In their scenario, the sweep was only the most recent of possibly several changes under selection to this gene. This most recent one involved a regulatory change within exon 7 of the gene that did not affect the coding sequence at all.

    The sequence analysis carried out by Maricic and colleagues is very straightforward. They simply resequenced the gene region from Neandertal specimens to get a list of sites where Neandertals and Denisovans do not carry a derived human variant, and then resequenced the gene in 50 humans to see how many of the derived human mutations are high-frequency. The one they identify is both high-frequency and affects a candidate regulatory site. The site is a binding site for the transcription factor POU3F2. The rest of the paper documents their attempts to demonstrate an effect of this site on gene regulation in tissue culture. They conclude:

    The transcription factor POU3F2 is expressed exclusively in the central nervous system (Schreiber et al. 1993), more specifically in postmitotic neurons and glia (Hagino-Yamagishi et al. 1997). Within the central nervous system, FOXP2 is expressed in postmitotic neurons (Ferland et al. 2003). Thus, it is reasonable to assume that POU3F2 regulates expression of FOXP2 in neurons. It is furthermore interesting that position 114076877 is located at the point in intron 8 of the FOXP2 gene where the pattern of allele frequencies among humans indicates that a functional change occurred that could be responsible for a positive selective sweep affecting the FOXP2 gene during the last 50,000 years (Coop et al. 2008). It is noteworthy that this is the only nucleotide variant in that region where the majority of present-day people carry a derived variant that is not present in Neandertals and Denisovans. Thus, it is possible that this change was positively selected recently during the evolution of fully modern humans.

    However, the ancestral allele shared by Neandertals and Denisovans is also fairly common in some human populations today. As Maricic and colleagues conclude, the obvious thing to do is look at homozygote carriers of the allele to see if they're different from noncarriers:

    The ancestral allele occurs at frequencies of ∼10% in some African populations (supplementary table S6, Supplementary Material online). Therefore, individuals homozygous for the ancestral allele can be expected to occur at a frequency of approximately 1% in the population. In such individuals, the phenotype of the ancestral allele should be observable even if is recessive to the derived allele. Further work will explore the phenotypes of such homozygous carriers of the ancestral allele and the consequences of the substitution at position 114076877 on FOXP2 transcription in model systems.

    This all seems logical. We may not be able to say that Neandertals were just like us in FOXP2 -- but that's because we're not all alike. They're just like some of us.

    The only thing I would add is that the number of humans covered by the study is still quite small. The paper examined only 50 individuals from the HGDP set; additionally they considered the 1000 Genomes data. It is interesting that the Neandertal-Denisovan ancestral allele at this site is not present in several of the samples outside Africa in the 1000 Genomes data, but it is present in two of the American samples, and in all the African samples. So although the region looks like it was positively selected at some point during the last 100,000 years or so, we still can't yet say that the ancestral allele carried by Neandertals was disadvantageous within later populations.

    Larger samples would settle that question. In the meantime, this study does point the way toward a wider analysis of differences in gene regulation among archaic human genomes.


    References

    Synopsis: 
    A discovery of gene regulation differences in FOXP2 may explain the variation of the gene in recent and archaic people.
  • When Hollywood and paleoanthropology intersect, 2

    Mon, 2013-01-28 23:43 -- John Hawks

    A couple of weeks ago, TV's Bones series, which features stories inspired by forensic anthropologist Kathy Reichs, did an episode with a relevant plot: The FBI encounters bones dug up by an archaeologist in Chechnya, which turn out to be Ayla's family, or something thereabouts -- a family group of Neandertal, modern human, and hybrid offspring. A reader tipped me to the story, but I'm not a regular viewer of the show. Fortunately, Kristina Killgrove -- along with her excellent work in Roman bioarchaeology -- also watches and reviews episodes of Bones: "Bones - Season 8, Episode 11 (Review)".

    She describes the plot and applies the reality filter -- including things the writers got right, and the parts that were, well, weaker:

    Edison said "epiphynis" for some odd reason. He and Brennan both kept saying "Homo sapien" which really just annoys the crap out of me. (Seriously, I harp on this with my students - it's sapiens, as it's from the Latin present participle, which ends in -ns. Also, it's super easy to remember it has an -s at the end because literally all other major Homo species do: H. habilis, H. erectus, H. neanderthalensis, and H. sapiens. For different linguistic reasons, but it makes it easy to remember!) I could go on and on about how they kept saying "Neanderthal" rather than "Neandertal" (the latter being the preferred pronunciation today), but... yeah. Argh. Just. Argh.

    The plot twist of the creationist who funded archaeological work so that he could destroy the finds was pretty clever.

  • Send in the clones

    Sun, 2013-01-27 00:46 -- John Hawks

    I didn't comment on the Neandertal cloning kerfuffle this week. Now that it's sort of died down, I'll provide a link to a Knight Science Journalism Tracker story by Faye Flam that gives some context and timeline: "Weird Science: The Attack of the Neanderthal Clone Baby Stories".

    What reader could resist clicking on a headline about a mad scientist trying to find women to carry Neanderthal clones? It sounds like something from the old supermarket tabloid the Weekly World News, but this latest whopper is loosely based on a real statement by a real scientist.

    In his book, Regenesis, written with Ed Regis, Harvard researcher George Church really did say that it might be possible to clone Neanderthal babies using the Neanderthal genome sequence reconstructed with synthetic biology. And the kicker: A cloned embryo of our extinct cousin could be gestated by an “adventurous” woman. (On the plus side, the first volunteer would be shoe-in to get her own reality show.)

    I heard from a few readers this week who wanted to know (a) if Church is really close to cloning a Neandertal, and (b) where they could sign up.

    The answer is that this isn't going to be technically possible for quite some time. This is not the same problem as cloning a living person. A living cell can provide functional genetic material that can be used to generate a cloned cell. Neandertal skeletal remains have DNA only in very short, nonfunctional bits. Taking genetic information and making it into a working chromosome is a very substantial technical challenge, and ensuring that the genetic information is free of errors and capable of yielding a viable embryo will be massively difficult. Church is an optimist about the rate of progress on these problems, and I have correspondents who think these advances may happen in less than ten years. Personally I think it will be more than thirty.

    By that time, human cloning will probably be routine.

    Some people are not that interested in understanding the technology, they just want to talk about ethics. That's why so many press outlets picked up the story, and why Church tried to walk back his comments after they received such wide press. I have some thoughts about the ethical aspects of cloning as applied to Neandertals, but they'll take some more time and space to describe.

  • Neandertal anti-defamation files, 18

    Sun, 2013-01-13 23:37 -- John Hawks

    I recently ran across a book of relationship advice by John V. Farrar, titled Dump the Neanderthal; Choose Your Prime Mate.

    OK, yes, seriously. Dump the Neanderthal.

    Here's a passage:

    The image of the Neanderthal was chosen for the title of this book because it seemed to epitomize the notion of an insensitive, thoughtless and, perhaps at times, an even brutish partner. Neanderthal-like behavior may not necessarily be physical, but it is always discounting of the wishes and feelings of his partner. A dysfunctional, unhealthy relationship does not exhibit either fairness or balance. The Neanderthal-like male says whatever he feels like saying, while she carefully watches her words. She does the cooking while he does all the eating. He abuses, and she gets abused. And so on. There is an imbalance in both effort and power. While she may be the breadwinner, for example, he may control the finances. She may work harder than he does to be sexually attractive, but he dictates their physical life together. As a result, the woman in these relationships manifests the stereotypical emotions of guilt, frustration, and mental exhaustion.

    This guy is clearly worse than Broud from Clan of the Cave Bear. All the worst stereotypes. Can't therapists leave these poor ancient people alone? First Talia Shire, and now this!

    I mean, seriously -- you want a modern, feeling partner, you can't do better than a real Neandertal.

    You can rest assured: If you see me write "Dump the Neanderthal", it's about spelling the word without the "h".

  • Neandertal humanities

    Thu, 2013-01-03 20:32 -- John Hawks
    Research authors: 
    Publication information: 

    In press in Consilience, edited by Joe Carroll

    Work status: 

    This manuscript has just been added to the open research queue. Until this status is updated, readers can assume that the manuscript is incomplete and essential parts are being added by one or more authors. It may be an extremely early draft upload awaiting editing and addition of citations, so reader beware.

    The dead speak to us through their leavings. Material objects left by ancient preliterate peoples—including their bodies—are the only possible carriers of significance to us today.

    I study Neandertals, ancient people lived more than 30,000 years ago in Europe and western Asia. I have no Neandertal informants. No matter how often I ask them questions, they will never answer. They left no video, no books, no inscriptions. They left stones and cutmarked bones, a few postholes and pits, bodies and ash.

    I seek to understand the lives of these ancient people. I struggle to gain insight into their humanity. Unquestionably they had rich social lives. No social primate can function without emotion, without affiliations or conflicts, without long memories of experiences with other individuals. No primate that depended on hunting and gathering, as all members of our genus have done, could survive without deep social bonds that enabled cooperation and mutual interest.

    Yet the Neandertals remain enigmatic. In a few exceptional cases, they carved regular lines upon objects. An optimist can point to a handful of clear indications of intentional behavior, giving the humanist some hope of treating them like texts that can in principle be interpreted. A pessimist replies that whatever "texts" remain are written in an undecipherable script.

    What would Neandertal humanities be like? The question is not trivial; it is emblematic of a deep problem in anthropology. Can we understand the subjective lives of other cultures? If so, what methods will bring us toward such a knowledge of ancient people? It may appear that all attempts to build knowledge about the subjective lives of ancient people are necessarily fictional.

    Throughout this essay, I consider the problem of Neandertal intentional markings. This is a rich area of inquiry in archaeology, with more and more evidence of Neandertal "symbolic" behavior emerging every year. As much as we might wish it, intentional markings do not provide "windows" into the minds of ancient people. As described below, some past efforts to explain such markings cannot be distinguished from fiction. Yet, if the subjective lives of ancient people must forever remain unknown to us, then surely our attempts to interpret the lives of our contemporaries must be equally fictional. Consilience, as a general attitude about the ability of scientific knowledge to cross into humanistic realms, holds out the promise that we might study and come to an understanding of the humanity of ancient people, not only as social primates but also as subjects of experience. But I have little confidence that science can provide such knowledge, or that non-science interpretive approaches can create knowledge distinguishable from fiction.

    ***

    Anthropology is a diverse field. Biological anthropologists, like me, study the human organism and its evolution. Like all organisms, humans exhibit behaviors that may adapt them to their environments. For humans, the social environment is a primary determinant of the adaptive constraints shaping behavior. Our social lives are a niche that we continually construct, our conscious selves are tools for our nervous system to navigate this social environment. Subjective experience, in this way of thinking, is fundamental to human biology. Without it, we could not function in our social environments.

    Many anthropologists study human behavior not from a scientific perspective, but within an interpretive frame. The interpretive anthropologist recognizes that a person's behaviors may not be fully translatable into different cultural contexts. Indeed, even interpretation within the subject's own cultural context may be unsatisfying. Identifying the proximate or ultimate causes of behavior or belief is not the goal of interpretive theory; the interpretive anthropologist may not even find interesting such reduction of subjective experience to physical causes. Theory, to the interpretive anthropologist, is a productive and creative activity, a synthesis of observation with the interpretive frame. By observing the subjective experience of another person and her own encounter with the literature, the interpretive anthropologist builds something new.

    I consider myself a scientist. Some interpretive anthropologists reject scientific approaches and methods, describing them at best as irrelevant to understanding subjective experience; at worst weapons of hegemony.

    I consider myself a humanist. In academic discourse within anthropology, the interpretive approach is aligned with humanistic inquiry. My work is starkly different in its goals and methods from the interpretive anthropologist. Like many of my colleagues I pick my way through this minefield. Subjective human experience must have an evolutionary origin, which we seek to understand and discover.

    ***

    Obviously, the broad concept of "consilience" is relevant to any interdisciplinary inquiry. Whewell's "consilience of induction" [1] is an important mode of argument in biological anthropology, just as in evolutionary biology [2]. Whewell held that consilience of inductions from two classes of facts "is a test of the truth of the Theory in which it occurs". E. O. Wilson's argument for consilience of different fields of knowledge [3] is rather grander in scope than Whewell's conception. From his 1998 essay on the subject (p. 133):

    Consilience proved to be the light and way of the natural sciences. Physics, with its astonishing congruity to mathematics, came to undergird chemistry, which in turn proved foundational for biology. The successful union was not just a broad theoretical consistency, as articulated by Whewell, but an exact unfolding of principles pertaining to more complex and particular systems into the principles for simpler and more general systems.

    Wilson discarded Whewell's reference to induction, and argued that the fact of consilience is a logical consequence of the reduction of chemical and biological theories to physical theories. Consilience was itself, in Wilson's description, substantially easier to establish than reduction. A scientist can observe that two statements at different levels of physical complexity are consilient without being immediately able to reduce the complex system to a simpler one. For example, the ratio of stable carbon isotopes in a mammal's tooth enamel reflects the photosynthetic pathway of plants eaten by the individual during the period of enamel formation. Eaters of grasses with a four-carbon photosynthetic pathway have enamel with a higher proportion of carbon-13 than do eaters of fruit and leaves from trees with a three-carbon photosynthetic pathway. This hypothesis relies on consilience of theories underlying the physical properties of carbon isotopes, the chemistry of photosynthesis in plants, and the biology of enamel formation in mammals. Yet we cannot presently reduce the embryonic development of ameloblasts (enamel-forming cells) to physical principles. Nor can we synthesize, or build up, the actions of ameloblasts from chemical or physical theories. In practice we make a much weaker assumption: that these cells will not betray well-known principles or act according to their own idiosyncratic physics. Discussing reduction and synthesis, Wilson admitted the difficulty (and in some cases, impossibility) of building predictive hypotheses about complex systems from simple physical principles. He referred explicitly to the "paradox of emergence" which necessitates that levels of organization have their own proper explanatory theories.

    Our attempts to understand retrospectively the results of complex interactions may demonstrate the fact of consilience among explanatory theories that apply to different levels of interaction. Does the fact of consilience prove that the explanatory theories at different levels reduce to a common set of simpler (presumably physical) principles? To the extent that we believe in a single material reality, we must conclude Wilson is correct. When we have theories at different levels that are more-or-less true, they should give rise to consilient inductions. If theories at different levels give rise to different predictions about the same physical event, they are by definition incompatible. If theories always give rise to the same prediction about every possible event, they are by definition identical. Consilience is no proof of reducibility, but it may serve as a sign of reducibility.

    ***

    But what if our theories are not close to the truth?

    The question may seem impish: After all, if our theories are so wrong, why would we bother? But the idea that similarity of predictions is an indication of similarity of theories, which seems plausible for the recent history of physical sciences, simply doesn't work in the social sciences and humanities. Replacing Newton's theory of gravitation with Einstein's was a tiny change for most easily observed physical systems, so tiny that we still teach Newton's theory to our children as correct. The history of the social sciences is a march through dozens of all-encompassing social theories with barely any attempt to falsify or test for their mutual incompatibility. Today's interpretive anthropologists flock among a confusing array of social theorists, each with different, partly incommensurable schemes of social explanation.

    Consider for example the phenomenon of religious ritual. Counting only the last two hundred years, theories of the social and psychological causes of religious ritual have been promulgated by dozens of major scholars, including Tylor, Spencer, Freud, William James, Durkheim, Boas, Campbell, and our contemporaries Pascal Boyer and Scott Atran. Most among this group have attempted comparative procedures similar in form to the consilience of inductions. The subject of religion almost demands such an approach, as it touches on so many aspects of human interactions, and is understood through different religious traditions in different cultural groups.

    An example close to the Neandertals is provided by George Barton, who argued that religious ritual remains as a legacy of prehistoric peoples' awe of the divine feminine [4].

    Palæolithic religion was, then, sex-mysticism. The psychologic unity of the race made it universal as its survivals in the historic period prove. This is the real origin of religion. It was not begotten by fear (Lucretius), nor by animism (Tylor), nor by ancestor worship (Herbert Spencer), nor by the mysterium tremendum (Otto), but by the mysterium feminium—a mysterium tremendum indeed, but scarcely that which Otto contemplated.

    Barton turned to the study of myth and religion in small-scale societies, as well as the mortuary practices of Paleolithic people, to make the argument that ritual had its origin in the worship of females:

    Dr. Lewis has pointed out that in the case of such burials the body of the dead is covered with red earth and often either rests upon or is partly covered with the shells of various kinds of shellfish. He rightly infers that the image represented the mother-goddess— the goddess of life—that the red earth represented blood, the vehicle of life, and that the shells were emblems of the mother goddess because, like her, they contained life or produced a living creature. [4]

    Neanderthals never to our knowledge painted figures or other representations on the walls of caves. Nor did they accompany burials with pigments as did some later European peoples. But some red marks on the walls of caves are now known to be contemporary with late Neanderthals, raising the possibility that they were the authors of this behavior. Pigment crayons, blocks of mineral pigment that have been worn by rubbing on some surface, have long been known from Neanderthal sites. A recent forensic analysis of such crayons has shown that some of them were rubbed on a soft surface, such as skin or hide [5]. At two sites, small cup shaped pieces of stony stalagmite have been found with traces of mineral pigment inside them. The Neanderthals appear to have been painting, or mixing mineral pigment for some other purpose. Evidence of shellfish exploitation is rarely found that Neanderthal sites, possibly because the lower sea level during Neanderthal times meant that shorelines were far from today's sites in most of Europe. Nevertheless a handful of sites show that Neanderthals were using shellfish and other marine resources [6], and at one site Neanderthals were gathering empty shells with natural holes, apparently stringing them together. One Iberian site preserves an exceptional shell bearing a natural band of pigment on one side and on the other, painted by a Neanderthal, a red ochre band mirroring the opposite side [7].

    With this kind of evidence emerging from the archaeological record of Neandertals, perhaps we can test such hypotheses as Barton's for the origin of religious ritual. Barton's work does not stand alone: Several scholars have pursued similar models for the origin of religion, relating red pigment, female symbolism, and the origin of religious ritual or broader social interactions (e.g., [8], [9]). Menstruation in this view ties blood with the social power to govern sexual relations, as women in a number of societies undergo an involuntary seclusion at the time of menstruation. Fertility is a mysterious and powerful process within many societies, and menstruation visibly connects fertility with blood. A connection of religious ritual and the sacred feminine reads like the Da Vinci Code of Paleolithic archaeology, depending on observations drawn from ethnography, folklore, political economy, art, and Paleolithic archaeology. In Knight's model, as an example, the appearance of complex social interactions, symbolic behavior and language is explained by a sexual revolution in which women gained meat and protection from men by controlling sexual access [9]. Knight and others have tied these phenomena to ethnographic and economic observations among African and Australian small-scale societies, tying them further to the iconography of rock art.

    What should we make of this seemingly plausible hypothesis of a causal connection of religious ritual, menstruation, motherhood, shells, the color red? I suggest that the idea is an "umbrella hypothesis" [10], an attempt to explain a large set of true or uncontroversial propositions as results of a single underlying cause. An umbrella hypothesis is not necessarily false, or even problematic. But the strength of support of the hypothesis is not a function of the facts adduced in its favor. Indeed, the hypothesis does not necessitate that any of these propositions be true; if one were false, some other proposition might otherwise have been found as support for the hypothesis. An umbrella hypothesis subtends an internally consistent model of causal relations among facts.

    How can we explain the association of red pigment with burials and Paleolithic art without a causal relation among menstruation, religious ritual and art? Red ochre, the second most common pigment in archaeological sites after black, is much easier to obtain and survives better in archaeological contexts than most other color pigments. Likewise shells are archaeologically durable and widely collected and traded in nearly all preindustrial societies. Symbolic association of the color red with blood is ubiquitous, even inevitable. But other correlates of red vary widely across cultures, in some generally positive, others negative, some masculine and others feminine [8]. To be sure, some traditional African groups have placed enormous social and economic importance on red cosmetics, associating them with menstruation and status. These elaborate traditions leave heavy material traces, from the acquisition, distribution and use of red pigments, and not a trace of such elaborate material traditions can be found in the Paleolithic record. Instead, we have traces of red ochre use, scattered across much of the Old World during the last 300,000 years, with a handful of co-occurrences with shells.

    We are not looking at a consilience of red ochre burials, shells, and mother-goddess ideation, we are looking at a coincidence of these things in some material and cultural contexts.

    From a purely interpretive perspective, it may not matter that the coincidence is accidental. The strong association of menstruation and red pigment in the ideological systems of some societies is a fact that has braced the social lives of thousands of people, across hundreds of years. People's subjective experiences within such cultural contexts have included these social facts, by which people have navigated their social lives. Interpretation of these facts is a form of play, sometimes reversing hypotheses of cause, connecting them to the work of social theorists, reading them as if they were a text through an interpretive frame. But to apply this frame outside the context where it is observed — to extend it to Neandertals or other Paleolithic peoples — is fiction.

    ***

    The scientist wants more than to interpret the associations where they occur; she wants to predict, to deduce, to infer unknowns. And for this, she needs far more than the observation of their occurrence together. She must show the associated facts to be causally connected. A statistical association between the elements of the hypothesis, the red pigment, shells, symbols of the feminine, and rituals related to menstruation in recent human cultures might test the hypothesis of causal connection among them. A consistent record of ideational connection from informant interviews might also contribute to such a test, or a deeper record of archaeological shell use by Paleolithic people. Such evidence helps to substantiate that the inference as applied to ancient humans may be more than fiction. Such evidence drawn from several different lines of inquiry might contribute to a consilience of inductions. Because such an approach must be tied to more lines of evidence, we must necessarily proceed more slowly than the purely interpretive anthropologist. We must also spend more time on each line of evidence establishing the direction and strength of causal relations among observations.

    More than 20 years ago, most archaeologists held that only modern human groups show clear evidence of intentionally marking objects for the purpose of communicating. The upper Paleolithic record of artistic expression is vast and unparalleled by anything that came before it. When a visitor today walks through a cave with art painted on the walls, she experiences a reality of iconic expression that simply did not exist anywhere in the world before 50,000 years ago. Painted art, sculpture, musical instruments, and other nonvocal modes of communication appeared in the archaeological record of Europe, Australia, and Southern Africa within the span from 80,000 to 30,000 years ago. Some archaeologists have dubbed this phenomenon “the human revolution”, noting that provides the first evidence that human minds had become truly subjects of experience [11].

    This view has become increasingly problematic as evidence of the capabilities of Neanderthals and other archaic humans has grown [12]. As noted above, the exceptional evidence of intentional marking by Neandertals contributes to this record. More evidence comes from the growing record of behavioral sophistication among African peoples of the Middle Stone Age period, earlier than 70,000 years ago. At several sites, including some relatively far from the seashore, pierced shells have been found [13]. Ostrich eggshells were incised with geometric patterns in southern Africa as early as 80,000 years ago [14]. A tradition of pigment use, including the complex preparation of mixtures, is of equivalent age in southern Africa as in Europe, in both cases dating long before the origin of modern human populations.

    Faced with these facts, archaeologists have problematized the origin of marking behavior. At one extreme some suggest that we should maintain the null hypothesis that archaic people had cognitive capabilities identical to those of living humans. From this point of view evidence of marking, pigment use, or the accumulation of nonutilitarian objects such as shells, supports the interpretation that the symbolic communication abilities of humans extend far back into the Pleistocene. At the opposite end of the scale, we can observe that many of the archaeological cultures of the last 10,000 years failed to show systematic evidence of marking, gathering of exotic objects, or other archaeological indicators of nonvocal communication [15]. The lack of such evidence does not indicate that these recent peoples were incapable of such activities; it merely reflects an ecological or social context in which people did not value the production of such material objects.

    Archaeologists have begun to consider models for the gradual emergence of such cognitive abilities in archaic humans. Within Africa the sophistication and standardization of stone tool technology increased across the last 300,000 years. The appearance of small projectile points, long-distance movement of raw material, and increasing pigment use during the last 100,000 years seems a logical extension of a much longer-term process [16]. Likewise European Neanderthal populations show a gradual increase in sophistication of tool raw material acquisition, stronger evidence of a diversity of material culture, and pigment used in marking behavior over the same time period. Just as genetic evidence has made the genealogical connection between living people and archaic people more complex, so the archaeological record has made the interpretation of behavioral capabilities in these ancient people more complex.

    Our growing knowledge of Neandertal marking behavior shares little with the interpretive approaches of cultural anthropology. We see only hints and traces of the behavior of a few Neanderthals at a handful of instants in their lives. With the cave art of the Upper Paleolithic, the art historian can use interpretive methods to add value to our understanding. She may not be able to read the minds of the artists, but she can arrive at an understanding of their stylistic processes, the relation of representation to their lives, and the picture of their social existence. The archaeologist Dale Guthrie brings a contextual understanding to Paleolithic art built upon his experience as a hunter and his consideration of Paleolithic groups [17]. The consistent representation of what he calls “high testosterone activities” helps to place the role of the artist within their hunting society. The representations of animals attend to small details of their biology, such as rutting male deer, animals at the peak fat distribution of autumn, and prowling carnivores, testify to the intimate ecological knowledge of the artists. Meanwhile, the distribution of handprint sizes shows that children were often among the artists, an inference supported by the relatively crude form of a large majority of representations seldom illustrated in books about cave art. The understanding attained by the art historian about these ancient people is not dialogic, not negotiated, nor is it based directly on testimony. But it is undeniably humanistic.

    With Neanderthals and their contemporaries we can approach their humanity only through a fog. Drips of red ocher in the dust of an ancient site [18] do not speak of their maker. They do not even have a maker in the sense of an author of intention behind their production. Repeated marks upon a bone may reflect intention, but ascribing intention requires ruling out alternatives that may in practical terms be impossible to exclude for a singular object.

    Still, our inability to arrive at a symbolic or iconic understanding of Neanderthal production does not preclude a truly humanistic understanding of them. A humanistic interpretation of the cave art of the Upper Paleolithic cave art depends on much more than the content of the images themselves. Such an understanding can be built by juxtaposing the content of the art with a sophisticated knowledge of hunting practice tied to a depth of ethnographic knowledge about human foraging and social interactions in small groups. When we have a blind spot of interpretation, it is because we assume too much, not because the paintings tell us too little. In other words humanistic understanding in this applied the context does depend on a consilience of inductions in the Whewellian sense.

    ***

    The remains of the Neandertals and other ancient peoples do speak to us. We can develop some knowledge about the subjective lives of these people. But this knowledge is necessarily limited, and can be attained only very slowly.

    Anthropologists approach the problem of understanding subjective experience in two ways. Scientific anthropologists approach the problem with great caution, proceeding slowly and by degrees building understanding of small parts of the overall picture. Interpretive anthropologists implicitly exercise even greater caution, by assuming that subjective experience may never be comprehensible even in principle. They therefore focus on the aesthetics of an improvised encounter between observation and theory.

    I do not deny that the interpretive approach can yield interesting and compelling stories. The methods and style of humanistic and interpretive anthropology are not sterile; they actively bring new perspectives on the observations made by ethnographers and other cultural anthropologists. But it is not in the nature of such interpretive methods to comport with the requirements of hypothesis testing. I assert that these approaches really cannot be reconciled, in the Wilson's sense of consilience. The aims of interpretive anthropology are productive and aesthetic in nature. This is not a misunderstanding within anthropology, it is a real difference of priorities. Interpretive anthropology cannot be reduced, even in principle, to scientific principles of biology or psychology.

    Sometimes I despair that the noise of exuberant interpretive work may drown out the quiet signal as we slowly build up multiple lines of evidence about the lives of ancient people. We are building a humanistic understanding of Neandertals and other ancient people. We may never know the songs of Neandertals, but we will someday know whether any songs could have existed. We may never find a Neandertal portrait, but we will assemble an understanding of how pigment marking once fit within now-extinct social systems. It diminishes the humanities to restrict them to mere interpretation.


    References

    1. Whewell WH. The Philosophy of the Inductive Sciences: Founded Upon Their History. London: J. & J.J. Deighton; 1840.
    2. Gould SJ. The Structure of Evolutionary Theory. Cambridge, MA: Harvard University Press; 2002.
    3. Wilson EO. Consilience among the Great Branches of Learning. Daedalus [Internet]. 1998;127:pp. 131-149. Available from: http://www.jstor.org/stable/20027479
    4. Barton GA. The Palæolithic Beginnings of Religion-An Interpretation. Proceedings of the American Philosophical Society [Internet]. 1940;82:pp. 131-149. Available from: http://www.jstor.org/stable/985012
    5. Soressi M, D'Errico F. Pigments, gravures, parures: Les comportements symboliques controversés des Néandertaliens. In: Les Néandertaliens. Biologie et cultures. Les Néandertaliens. Biologie et cultures. Paris: Éditions du CTHS; 2007. pp. 297-309.
    6. Barton N. {Mousterian} Hearths and Shellfish: Late {Neanderthal} Activities on {Gibraltar}. In: Stringer CB, Barton RNE, Finlayson JC Neanderthals on the Edge: Papers from a Conference Marking the 150th Anniversary of the Forbes' Quarry Discovery, Gibraltar. Neanderthals on the Edge: Papers from a Conference Marking the 150th Anniversary of the Forbes' Quarry Discovery, Gibraltar. Oxford, UK: Oxbow Books; 2000. pp. 211–220.
    7. Zilhão J, Angelucci DE, Badal-García E, D'Errico F, Daniel F, Dayet L, Douka K, Higham TFG, Martínez-Sánchez MJ, Montes-Bernárdez R, et al. Symbolic use of marine shells and mineral pigments by Iberian Neandertals. Proceedings of the National Academy of Sciences of the United States of America. 2010;107(3):1023-8.
    8. Wreschner EE. Red ochre and human evolution: a case for discussion. Current Anthropology. 1980;21:631–644.
    9. Knight C. Blood Relations: Menstruation and the Origins of Culture. New Haven: Yale University Press ; 1995.
    10. Langdon JH. Umbrella Hypotheses and Parsimony in Human Evolution: A Critique of the {Aquatic Ape Hypothesis}. Journal of Human Evolution. 1997;33:479–494.
    11. Mellars PA, Stringer C. Introduction. In: Mellars P, Stringer CB The Human Revolution: Behavioural and Biological Perspectives on the Origins of Modern Humans. The Human Revolution: Behavioural and Biological Perspectives on the Origins of Modern Humans. Edinburgh: Edinburgh University Press; 1989. pp. 1–14.
    12. D'Errico F. The Invisible Frontier: A Multiple Species Model for the Origin of Behavioral Modernity. Evolutionary Anthropology. 2003;12:188–202.
    13. Bouzouggar A, Barton N, Vanhaeren M, D'Errico F, Collcutt S, Higham T, Hodge E, Parfitt S, Rhodes E, Schwenninger J-L, et al. 82,000-Year-Old Shell Beads from {North Africa} and Implications for the Origins of Modern Human Behavior. Proceedings of the National Academy of Sciences, U. S. A. [Internet]. 2007;104:9964–9969. Available from: http://dx.doi.org/10.1073/pnas.0703877104
    14. Texier P-J, Porraz G, Parkington J, Rigaud J-P, Poggenpoel C, Miller C, Tribolo C, Cartwright C, Coudenneau A, Klein R, et al. A Howiesons Poort tradition of engraving ostrich eggshell containers dated to 60,000 years ago at Diepkloof Rock Shelter, South Africa. Proceedings of the National Academy of Sciences [Internet]. 2010;107:6180–6185. Available from: http://dx.doi.org/10.1073/pnas.0913047107
    15. Speth JD. News Flash: Negative Evidence Convicts {Neanderthals} of Gross Mental Incompetence. World Archaeology [Internet]. 2004;36:519–526. Available from: http://dx.doi.org/10.1080/0043824042000303692
    16. McBrearty S, Brooks AS. The revolution that wasn't: a new interpretation of the origin of modern human behavior. J Hum Evol. 2000;39(5):453-563.
    17. Guthrie DR. The Nature of Paleolithic Art. 1st ed. University Of Chicago Press; 2006. Available from: http://www.amazon.com/exec/obidos/redirect?tag=citeulike07-20&path=ASIN/0226311260
    18. Roebroeks W, Sier MJ, Nielsen TK, De Loecker D, Parés JM, Arps CES, Mücher HJ. Use of red ochre by early Neandertals. Proceedings of the National Academy of Sciences [Internet]. 2012. Available from: http://www.pnas.org/content/early/2012/01/17/1112261109.abstract
  • Slow cooking Neandertal subsistence

    Tue, 2013-01-01 20:12 -- John Hawks

    During the past couple of years, new evidence has really shifted our view of Neandertal diet. Even three years ago, it was not unusual to hear Neandertals described as "hypercarnivores", more heavily reliant upon meat than any living hunter-gatherers, except possibly for Inuit who live on seal meat and whale blubber.

    The idea that Neandertals had diets with a very high fraction of meat -- maybe as high as 90-95% meat -- came from analyses of stable isotopes. I reviewed some of the stable isotope work on Neandertal diet in 2005 - "Neandertals noshed on mammoth meat?", "Neandertals: gone fishin' or not?". Here at the beginning of 2013, stable isotopes are well worth another review here on the blog.

    The extreme view of Neandertals as hypercarnivores has been softened by new evidence from several sources. Phytoliths and starch grains from Neandertal dental calculus have shown a wide variety of plants were consumed by Neandertals at least occasionally. Meanwhile, the starch grains have not only documented consumption of grains and tubers, but have also shown that Neandertals were cooking those plant foods. I wrote about the phytolith and starch granule discoveries by Amanda Henry and colleagues [1] last year ("Tartar control and Neandertal plant use").

    A new article by John Speth in Before Farming reconsiders the archaeological record of game exploitation by Neandertals and early modern humans in the Near East [2]. Speth begins with a short review of how Neandertals gradually came to be known as hypercarnivores -- in spite of many archaeologists' insistence that they must have been incompetent in various ways. After some discussion of the limits of the archaeological record, he notes that the zooarchaeological record doesn't tell us about the quantitative contribution of meat to the diet. In short:

    Lots of gazelle bones doesn’t necessarily mean lots of gazelle meat per capita per day.

    He illustrates this point with a historical case, the excavation of trash heaps from Fort Ligonier, Pennsylvania, occupied by the British during the French and Indian War. There, the total meat yield represented by animal bones was estimated at only 4,000 pounds, a tiny fraction of the meat ration known to have been issued to soldiers. The point of the example is that many biases prevent the accumulation and discovery of animal bone, even in historic contexts. The Paleolithic record of faunal exploitation can represent only the merest fraction of animal carcasses that were actually handled or consumed by ancient peoples. Biases guarantee that this record will be unrepresentative in ways that we may be poorly able to assess.

    Speth addresses the idea that Middle Pleistocene people consumed a very high fraction of meat by emphasizing that a diet of lean meat is unsustainable at such a level. If Neandertals' animal consumption was as high as Inuit peoples, then they must have been eating a high fraction of fat somehow:

    The Inuit or Eskimos provide a classic example of peoples whose traditional sustenance was provided almost entirely by meat, the diet commonly envisioned for cold-climate Neanderthals. But when looked at quantitatively, Inuit diet was actually composed primarily of fat, not lean meat, with the protein contribution seldom surpassing about 35 per cent of their calories, and usually lower, closer to 25 per cent. Pemmican, the traditional mainstay of Native Americans and First Nation peoples (‘Indians’) inhabiting the Great Plains of mid-continental North America, was a mixture of rendered fat and dried, pulverized lean meat, the mix carefully prepared so that the pro- tein component did not exceed 25–30 per cent of total energy (eg, Stefansson 1956; Speth 2010). In habitats where plant foods are neither abundant nor available for long periods of the year, and particularly for foragers in such habitats who do not store foods, fat becomes the principal non-protein macronutrient for much of the year. Foragers in the northern latitudes did obtain some carbohydrates by consuming fermented stomach contents of reindeer and ptarmigan, and sometimes inner bark (cambium), as well as small quantities of berries during the summer months (Eidlitz 1969; Gottesfeld 1992; Östlund et al 2009; Sandgathe & Hayden 2003; Zackrisson et al 2000). Until fairly recently, stomach contents were actually considered a delicacy (often referred to as ‘Eskimo ice cream’), not an emergency resource resorted to only when all else failed (Starks 2007; Speth 2010). Unfortunately, we lack quantitative data on the actual amounts that were consumed, how those amounts varied over the year, and whether men and women had comparable access. Did Neanderthals also con- sume fermented stomach contents? If so, would such a practice have had any detectable impact on their unusually high nitrogen isotope values?

    Through the middle of the article, Speth provides a detailed account of the biases due to taphonomy and ancient behavior that apply to faunal collections in Middle Paleolithic contexts. Many of these factors, such as biases in transport of different size animals, are well-known to archaeologists, but Speth's review will be useful for those who may not have studied the issue. The value of this part of the article is in its application of prey transport and landscape use to the unique geography of the Near East. Here, Middle Paleolithic peoples hunted amid water scarcity and temperature regimes that were very different from those found in Southwestern Europe. Yet by several indicators, the Middle Paleolithic population in both areas was relatively dense and successful.

    Speth reminds us that ancient hunters were active agents who made choices in their hunting strategies. Some of those choices may have been influenced by landscape use and prey abundance, but others are less easily predictable in such terms:

    The Hadza, one of the most thoroughly documented modern foraging populations, offer another interesting example. Wildebeest are one of the most abundant prey available to Hadza hunters, but they commonly avoid wildebeest in favour of zebras. Why? According to Hadza informants, the fat from wildebeest is hard and sticks to one’s teeth and palate,while zebra marrow and back-fat, especially the yellow subcutaneous deposits near the rump, are far more desirable (Oliver 1993:217; Selous 1907:220; Speth 2010:66–70). Were we to assume that Hadza hunters took prey in direct proportion to their availability on the landscape, our conclusions would be very wide of the mark.

    Back to the problem of lean meat: Hunter-gatherers in ethnographic and historical records have used boiling to degrease bone. This allows the use of the fat from inside the cancellous structure of the bone, which is a key resource supporting the use of lean wild animal meat. Boiling or slow-cooking using heated stones has been applied by many peoples around the world, and tends to leave a very distinctive archaeological trace -- the heated rocks, lined pits dug to enclose the slow-cooking mass, all show up in the archaeology. These techniques were not used by Middle Paleolithic people, or if such people used heated rocks, they did not use them terribly extensively. Stone boiling became common only later in the Upper Paleolithic of Europe.

    But Speth discusses other means of boiling, including the use of skin and bark containers. These are expedient and perishable, yet filled with water will effectively contain boiling liquid over hot coals or indirect flame. Whether such techniques were used by Neandertals remains speculative. The suggestion is latent in the identification of cooked starches within Neandertal dental calculus. If they were capable of cooking grains in moist heat, they must at least have been using bark packets or some other style of slow-cooking. The rendering of fat from bone by boiling in perishable containers would not take much additional innovation, and would have been energetically and nutritionally very advantageous.

    As I was discussing this with friends a couple of weeks ago, it occurred to me that the combination of cooked grains and meats within an animal bladder is a recurrent feature of the cuisine of Northern Europe. Neandertal haggis.


    References

    Synopsis: 
    An article about Middle Paleolithic subsistence brings a focus on meat acquisition

Pages

Subscribe to Neandertals

Neandertals

For years, I've worked on their bones. Now I'm working on their genes. Read more about the science studying these ancient people.

Denisova

From a finger bone of an ancient human came the record of a completely unexpected population. My lab is working on the science of the Denisova genome.

Acceleration

The advent of agriculture caused natural selection to speed up greatly in humans. We're uncovering some of the ways that populations have rapidly changed during the last 10,000 years.

Malapa

Just outside Johannesburg, the Malapa site is producing some of the most exciting finds in human evolution. This site is the headquarters of the Malapa Soft Tissue Project.