john hawks weblog

paleoanthropology, genetics and evolution

Philippines

  • Denisovan DNA in the islands, and an Australian genome

    Thu, 2011-09-22 18:09 -- John Hawks

    David Reich and colleagues today report on the persistence of Denisova-like ancestry in island Southeast Asia and Australia (citation not yet available). Meanwhile, Morten Rasmussen and colleagues (citation not yet available) report on the whole-genome sequencing of hair from an Aboriginal Australian who lived some 100 years ago.

    The most obvious story: These data utterly destroy the hypothesis of a single out-of-Africa colonization of Southeast Asia by modern humans. Many human geneticists have argued our present pattern of diversity originated in a wave of successive founder effects coming from a single recent African origin. They were wrong.

    Instead, we can turn to a complex model with successive dispersals and episodes of population mixture. This is not a static model of isolation-by-distance; it is a dynamic model in which populations grow and spread across large spans of the Old World, again and again and again. By my count, at least three massive episodes of population dispersal and mixture are necessary in Reich and colleagues' model. A picture of their admixture hypothesis:

    Denisova admixture model from Reich et al. 2011

    This model depicts (a) an early divergence of an African (represented by Yoruba) and Asian/Australasian populations. These mix with first Neandertals and then (for the Australian/New Guinea/Mamanwa populations) with Denisova-like people. Later (b), after the initial habitation of the Philippines by the ancestors of Mamanwa, a population like Andamanese Onge pushes into the islands, mixing with the ancestors of New Guinea and Australian populations. Later still (c), a population ancestral to today's Chinese people mixes with Philippines and other Southeast Asian people.

    As complicated as it looks, even this model must be a vast oversimplification. I don't like or attribute much belief to mixture models like this, as they assume too much about relative population sizes and the timing of mixture. Many recent hunting and gathering populations of Southeast Asia are not included in the current samples, and the Chinese sample is itself the result of very recent demographic events, covering what once may have been a wider diversity of peoples. Depicting Australian and New Guinean populations as monolithic is an artifact of the small sample; these places themselves housed a tremendous diversity of peoples. Nevertheless, the true model won't be simpler than this one; it will involve many more events that the data cannot yet resolve.

    Hints of that complexity emerge from the Aboriginal Australian whole genome. Rasmussen and colleagues show that this individual shares some ancestry with East Asian peoples, but on the whole populations in Europe and East Asia are much more genetically similar to each other than to this genome. The picture from the whole genome is essentially the same as that drawn by the SNP comparisons by Reich and colleagues, but with the potential (in the long run) to actually trace the histories of individual genes. And I think the gene-by-gene account of history will be important, because we already have some evidence that a few Denisovan genes do persist in mainland Asia, even though most are gone.

    To explain why, we can look at the proportion of Denisovan ancestry in different populations as depicted in a map by Reich and colleagues. The pie charts are confusing here, because they report the fraction of ancestry from Denisovans in each population relative to the 5% estimate for New Guinea. So Australians also have 5% in this figure, Timorese have around 2.5%, and Bougainville has more than 4%.

    Notice the apparent lack of Denisovan ancestry in anyone who lives anywhere that was once connected by land with mainland Asia. I say "apparent" deliberately: Abi-Rached and colleagues reported last month on the widespread distribution of Denisovan HLA types among today's Asian populations, and those may well be products of Denisovan genes that were later selected. I've already identified a handful of other loci that seem to reflect Denisovan ancestry in mainland Asian people. According to the comparisons by Reich and colleagues, such loci must be exceptions.

    At the same time, the mixture model presents an important idea: Once there were people in Southeast Asia who had much more Denisovan ancestry than any populations still remaining today. Both Australian/New Guinea populations and Philippine populations like the Mamanwa have subsequently mixed with new immigrants who lacked any sign of Denisovan ancestry. Prior to this later mixture, the ancestors of those populations must have been more Denisovan -- Reich and colleagues estimate 7%. This is the first evidence that ancestry from archaic people of Eurasia was diluted to a lower value by later population movements. If the population mixture originally happened somewhere in mainland Asia, any traces of Denisovan ancestry in those areas has been diluted almost to nonexistence. But the persistence of some genes would be predicted if natural selection were maintaining them in the face of demographic pressure from elsewhere.

    About the Australian genome, there will be much more interesting analyses to come, I expect. As whole-genome data come to represent more of the variation within human populations, we get a larger store of information about how we came to be variable. Variation traces not only to population movements and demography, but also to natural selection. Australia's population history has been very different from many populations of the Old World, and this genome should give us new perspective on the effects of that demographic history.

    Synopsis: 
    The hypothesis of a single out-of-Africa dispersal is rejected by new data about Denisovan mixture and whole-genome sequencing of an Aboriginal Australian.
  • A foot short

    Tue, 2010-06-22 06:26 -- John Hawks

    A single foot bone from a cave isn't ordinarily very remarkable. But when it's a funny-looking foot bone from a 67,000-year-old site on an island, that gets a little more attention. New in the Journal of Human Evolution, Arnand Mijares and colleagues report on a third metatarsal from a cave called Callao Cave, on the Philippines northern island of Luzon. If the date is right, this is the oldest human bone known from the Philippines, or indeed from anywhere not reachable by land from Asia -- except for the deepest bone elements from Liang Bua cave on Flores.

    The presence of a human bone on an island not reachable without a water crossing naturally brings up parallels to the Flores case. The bone's small size provides an additional parallel. Mijares and colleagues compare the metatarsal to a sample of small-bodied Negrito skeletal remains from the Philippines, finding that its dimensions are smaller than any of them. It is smaller in its preserved dimensions than the small metatarsal of OH8, generally assigned to Homo habilis.

    Did the bone belong to a hobbit-like creature?

    Sadly, there is no direct comparison to the foot bones of LB1, the skeleton from Flores that started the Homo floresiensis craze. This would seem to be another case where the failure to disseminate scans of a specimen has impeded the analysis of new discoveries from other sites. The science suffers for it. The description of the LB1 hindlimb elements by Jungers and colleagues (2009) includes good photos of the MT3 of that specimen, which looks basically humanlike, although small and with a small proximal end in particular.

    Human metatarsals have shafts that tend to get thinner as you move from the proximal to the distal end of the bone. The thinning is both in the side-to-side (mediolateral) dimension and in the top-to-bottom (dorso-plantar) dimension. The shaft in humans is relatively straight. Ape metatarsals tend to be very curved, and uniform in thickness from proximal to distal. Monkeys are between these extremes in curvature, although with substantial variability.

    The Callao MT3 is humanlike in being relatively straight and thinning from proximal to distal, at least in a mediolateral dimension. But the bone actually gets thicker in the dorso-plantar dimension as it approaches the head. That's not like most human metatarsals. The proximal end and shaft, which are well-preserved, are smaller in this Callao MT3 than in the females of the Negrito comparative sample examined by Mijares and colleagues. The proximal end and shaft are quite a bit smaller than the OH8 third metatarsal. This is a very small bone.

    Maybe too small. The metatarsal is reported to be smaller than OH8, with an estimated length just a hair longer than the measured length of LB1 MT3.

    I'd have to look at a lot more MT3's to be sure -- which I can't do right now -- but this one looks sort of funny to me. Could it be some other kind of primate? The authors hold out some possibility that the specimen represents a subadult, but if it does, it was very close to being adult based on the preserved anatomy. So it's not a case where the bone was going to grow a lot more. As usual, I wish that the paper included more information about the range of variation in humans and other primates. If we're dealing with an odd specimen, how strange is it in the characters that stand out?

    As for dating of the site, a mean of 67,000 years ago is the result of uranium-series dating of two cervid teeth in the same stratigraphic unit as the metatarsal. This method requires the application of a model of uranium absorption over the time since the teeth were deposited. This model is too complicated to describe here; the authors go through several scenarios and conclude that despite the possibility of inaccuracies, the remains are very unlikely to have been deposited as recently as 40,000 years (the approximate age represented by occupation of Niah Cave, Borneo). I have no reason to doubt the dating.

    I'll leave open the question of whether a date above 60,000 years ago is unexpectedly ancient for the region. It's interesting, at least. I see nothing impossible about there having been non-hobbit-ish humans in the area at that time, as I think we'll need to revise much about the timing of dispersal of mtDNA lineages from Africa. And don't forget that mtDNA doesn't tell the important story anymore.

    But by and large, I want more information on this one.

    (CORRECTION: The initial version of this post followed the paper in placing the site east of Wallace's line. Wallace's line actually passes south of the Philippines.)

    References:

    Jungers, W.L., Larson, W., Harcourt-Smith, W., Morwood, M.J., Sutikna, T., Rokhus Due Awe, Djubiantono, T., 2009. Descriptions of the lower limb skeleton of Homo floresiensis. J Hum Evol 57:538-554. doi:10.1016/j.jhevol.2008.08.014

    Mijares AS, Détroit F, Piper P, Grün R, Bellwood P, Aubert M, Champion G, Cuevas N, De Leon A, Dizon E. 2010. New evidence for a 67,000-year-old human presence at Callao Cave, Luzon, Philippines. J Hum Evol (in press) doi:10.1016/j.jhevol.2010.04.008

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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

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Acceleration

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Malapa

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