Category Archives: Middle Paleolithic

The oldest human footprints in Europe

By now I’m sure that the vast majority of readers of this blog, if not all, have already read the news about the Happisburg footprints, of almost one million years age, which are coincident with the earliest known dates for archaic human presence in Europe based on other archaeology (H. ergaster or antecessor) and extend their range quite further northwards. So I just want to post a reference, as the study is freely available online for all to read.

Nick Ashton et al., Hominin Footprints from Early Pleistocene Deposits at Happisburgh, UK. PLoS ONE 2014. Open accessLINK [doi:10.1371/journal.pone.0088329]


Investigations at Happisburgh, UK, have revealed the oldest known hominin footprint surface outside Africa at between ca. 1 million and 0.78 million years ago. The site has long been recognised for the preservation of sediments containing Early Pleistocene fauna and flora, but since 2005 has also yielded humanly made flint artefacts, extending the record of human occupation of northern Europe by at least 350,000 years. The sediments consist of sands, gravels and laminated silts laid down by a large river within the upper reaches of its estuary. In May 2013 extensive areas of the laminated sediments were exposed on the foreshore. On the surface of one of the laminated silt horizons a series of hollows was revealed in an area of ca. 12 m2. The surface was recorded using multi-image photogrammetry which showed that the hollows are distinctly elongated and the majority fall within the range of juvenile to adult hominin foot sizes. In many cases the arch and front/back of the foot can be identified and in one case the impression of toes can be seen. Using foot length to stature ratios, the hominins are estimated to have been between ca. 0.93 and 1.73 m in height, suggestive of a group of mixed ages. The orientation of the prints indicates movement in a southerly direction on mud-flats along the river edge. Early Pleistocene human fossils are extremely rare in Europe, with no evidence from the UK. The only known species in western Europe of a similar age is Homo antecessor, whose fossil remains have been found at Atapuerca, Spain. The foot sizes and estimated stature of the hominins from Happisburgh fall within the range derived from the fossil evidence of Homo antecessor.

Figure 8. Vertical image of Area A at Happisburgh.
a. Model of footprint surface generated from photogrammetric survey showing the 12 prints used in the metrical analyses of footprint size; b. Plot of length and width measurements of 12 prints showing possible individuals. Means and standard deviations for foot length and age for modern populations are also shown.
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Posted by on February 15, 2014 in European prehistory, Homo ergaster, Middle Paleolithic, UK


More details on the Neanderthal legacy in modern humans

Is straight hair Neanderthal?

A quick note on two recent studies on the relevance of Neanderthal introgression on modern Humankind, notably the “out of Africa” branch.

Sriran Sankararaman et al., The genomic landscape of Neanderthal ancestry in present-day humans. Nature 2014. Pay per viewLINK [doi:doi:10.1038/nature12961]


Genomic studies have shown that Neanderthals interbred with modern humans, and that non-Africans today are the products of this mixture1, 2. The antiquity of Neanderthal gene flow into modern humans means that genomic regions that derive from Neanderthals in any one human today are usually less than a hundred kilobases in size. However, Neanderthal haplotypes are also distinctive enough that several studies have been able to detect Neanderthal ancestry at specific loci1, 3, 4, 5, 6, 7, 8. We systematically infer Neanderthal haplotypes in the genomes of 1,004 present-day humans9. Regions that harbour a high frequency of Neanderthal alleles are enriched for genes affecting keratin filaments, suggesting that Neanderthal alleles may have helped modern humans to adapt to non-African environments. We identify multiple Neanderthal-derived alleles that confer risk for disease, suggesting that Neanderthal alleles continue to shape human biology. An unexpected finding is that regions with reduced Neanderthal ancestry are enriched in genes, implying selection to remove genetic material derived from Neanderthals. Genes that are more highly expressed in testes than in any other tissue are especially reduced in Neanderthal ancestry, and there is an approximately fivefold reduction of Neanderthal ancestry on the X chromosome, which is known from studies of diverse species to be especially dense in male hybrid sterility genes10, 11, 12. These results suggest that part of the explanation for genomic regions of reduced Neanderthal ancestry is Neanderthal alleles that caused decreased fertility in males when moved to a modern human genetic background.

B. Bernot & J.M. Akey, Resurrecting Surviving Neandertal Lineages from Modern Human Genomes. Science 2014. Pay per viewLINK [doi:10.1126/science.1245938]


Anatomically modern humans overlapped and mated with Neandertals such that non-African humans inherit ~1-3% of their genomes from Neandertal ancestors. We identified Neandertal lineages that persist in the DNA of modern humans, in whole-genome sequences from 379 European and 286 East Asian individuals, recovering over 15 Gb of introgressed sequence that spans ~20% of the Neandertal genome (FDR = 5%). Analyses of surviving archaic lineages suggests that there were fitness costs to hybridization, admixture occurred both before and subsequent to divergence of non-African modern humans, and Neandertals were a source of adaptive variation for loci involved in skin phenotypes. Our results provide a new avenue for paleogenomics studies, allowing substantial amounts of population-level DNA sequence information to be obtained from extinct groups even in the absence of fossilized remains.

I don’t have access to the papers (update: I do have the second one now) but, honestly, I don’t have time either, so, even with full access, I would have to be rather shallow, given the complexity of the matter.
Nevertheless I would highlight the following:
Fitness costs
Areas of dense gene presence tend to be more depleted of Neanderthal inheritance, meaning that, at least in many cases Neanderthal genes were deleterious (harmful) in the context of the H. sapiens genome. It’s probable that they worked better in their “native” context of the Neanderthal genome but we must not understimate the risks of low genetic diversity, a problem that affected Neanderthals as well as H. heidelbergensis (species probably including Denisovans or at least their non-Neanderthal ancestry).
Partial hybrid infertility
The areas of very low Neanderthal genetic influence include those of reproductive relevance, including genes affecting the testes and the chromosome X. This is typical of the hybrid infertility phenomenon, which is part of species divergence, making more difficult or even impossible that hybrids can reproduce. This particular item emphasizes that the differential speciation of Neanderthals and H. sapiens was in a quite advance stage already some 100 Ka ago, what does not seem too consistent with the lowest estimates for the divergence of both human species (H. sapiens have been diverging for some 200 Ka and are still perfectly inter-fertile). 
Adaptive Neanderthal hair introgression
On the other hand the Neanderthal genetic legacy has been best preserved in genes that appear to affect keratin (affecting skin, nails and hair). This bit I consider of particular interest because, based on the modern distribution of hair texture phenotypes, I have often speculated that straight hair may be a Neanderthal heritage and this finding seems supportive of my speculation.
It’s possible that straight hair conferred some sort of advantage in some of the new areas colonized by H. sapiens, maybe providing better insulation against rain or cold (the ancestral Sapiens thinly curly hair phenotype is probably an adaption to tropical climate, allowing for a ventilated insulation of the head).
Some 20% of the Neanderthal genome still lives in us
Collectively, that is. The actual expressed genes are probably a quite less important proportion anyhow and the actual individual Neanderthal legacy (expressing genes and junk together) seldom is greater than 3% in any case.

Neanderthals, Denisovans and everything else

A recent analysis of the nuclear DNA of a Neanderthal toe from Altai has caused widespread interest.
Kay Prüffer et al., The complete genome sequence of a Neanderthal from the Altai Mountains. Nature 2013. Pay per viewLINK [doi:10.1038/nature12886]
The story of a finger and a toe
Both the Denisovan and Neanderthal DNA sequences discussed in this paper come from small bones found at the same location: Denisova cave, Altai Republic. The Denisovan sequence that revolutionized human paleogenetics a few years ago corresponds to a finger phalanx bone of some 50,000 years ago. The less notorious Neanderthal sequence discussed in this study corresponds to a toe imal phalanx, which was found in a lower layer in the same gallery of the same cave, and hence should be older.
This is very interesting to underscore because it seems to imply that Neanderthals were in Altai and specifically in Denisova cave very early, at dates similar to those we find in West Asia (Tabun excepted) and they may even be older than Denisovans in the very cave that gave them their name.
The toe sequence was found in a previous study to have Neanderthal mtDNA, closely related to the lineages of European Neanderthals of various dates and sites. Instead the finger mtDNA (Denisovan) was derived from a more ancient branch of humankind than the very point of split between Neanderthals and modern humans (H. sapiens) and has been recently shown to be related to European H. heidelbergensis from Atapuerca
Notes in red are mine.
This study focuses on the autosomal DNA of both Neanderthals and Denisovans. Unlike mtDNA, whose phylogenetic position is simple and quite straightforward, autosomal or nuclear DNA (nDNA) is extremely much more complex to understand because of its recombining nature, requiring of statistical approaches, which may get extremely complex and potentially subject to premise biases. When comparing two individuals this gets largely simplified but it is a lot more complex when doing the same with larger samples.
And that is precisely what this study does: comparing one Denisovan, several Neanderthals and also several modern humans. Therefore it is a very complex paper and the authors necessarily assume some evaluation risks, which nevertheless are discussed in depth in the supplemental material, a methodology of the Pääbo team that we can’t but greatly appreciate.
Age estimates
The study makes two age estimates, one based on a very conservative and truly unbelievable Pan-Homo split date of 6.5 Ma BP and the other based on observed per generation mutation rates, which happens to be perfectly coincident with a Pan-Homo split of 13 Ma BP, the oldest extreme of Langergraber’s estimate. This coincidence alone is of enough relevance for all molecular clock approaches, because it effectively demands the doubling of all age estimates based on the ridiculously short 6.5 Ma Pan-Homo split supposition. 
Red outlines are mine. Click to enlarge.
It also produces a semi-reasonable San-West African age estimate of c. 86-130 Ka, although I would think it a bit older in fact or at the very least at the top end. This highlights the severe difficulties of such molecular clock estimates, because a 4 Ma divergence between the alleged introgressing mystery archaic in the Denisovan genome, seems out of the question according on the archaeological and paleontological record, which only documents Homo species since c. 2 Ma ago, half that time (within the estimate but clearly very far from the top end).
Altai Neanderthal inbreeding
An important finding of this study is that the studied individual was extremely inbred, with parents in effective relationship comparable to that of grandparent and grandchild or half siblings. This inbreeding tendency, even if extreme, is not so strange in populations that have experienced founder effect bottlenecks and small population sizes. The Denisovan and the modern human Karitiana people are not so extreme but range in the lower end of double first cousins level of genetic relationship between the parents. Other Native Americans like the Mixe are close to that range, while the other compared populations, Papuans and Sardinians, show much lower levels of inbreeding.
Whatever we may think of Altai Neanderthal inbreeding, their drift parameter is still very low when compared with European Neanderthals. This is not discussed in the paper but such extreme drift also seems to imply extreme inbreeding issues in European Neanderthals, even if these may have other causes such as an extremely strong founder effect or whatever.
Bonobo-specific segments were removed, so the bonobo position is not realistic.
Inferred population history
Both populations leading to the Altai Neanderthal and Denisovans, but not modern humans, appear to have gone through a strong decline in population size since hundreds of millennia ago. The Denisovan decline seems to begin c. 800 Ka ago while the Neanderthal one may have begun c. 500 Ka ago. While this is coincident with a general expansion of the H. sapiens branch (still undifferentiated in Africa), peaking around c. 250 Ka ago before differentiation and relative decline. In their words:

All genomes analysed show evidence of a reduction in population size that occurred sometime before 1.0 million years ago. Subsequently, the population ancestral to present-day humans increased in size,whereas the Altai and Denisovan ancestral populations decreased further in size. It is thus clear that the demographic histories of both archaic populations differ substantially from that of present-day humans.

Neanderthal and Denisovan admixture in modern humans

The new tests confirm in essence the previous findings: there is significant Neanderthal introgression in modern humans descending from the migrants out of Africa and there is also significant Denisovan one among Australasian populations.

Additionally and with some caution, the authors think that much lesser Denisovan introgression (of around 0.2%) is found among East Asians and that these, as well as Native Americans, show slightly more Neanderthal admixture than West Eurasians. In my understanding this may be caused by minor African flow to West Eurasia after the admixture event (and/or residual “First Arabian” persistence) and I would think that measuring South Asians would help to clarify this issue (because African admixture is negligible in the subcontinent but they are also distinct from East Asians).

These measurements are so weak that the authors agree to all kind of cautions about them in any case.

In addition to all this, the supplemental material (section 13) also detects tiny, almost homeopathic, amounts of Neanderthal gene flow to Yorubas (~0.02%), obviously mediated by H. sapiens backflow from Asia and Europe into parts of Africa, which eventually influenced other African populations. An even more diluted amount may also be present among the Mbuti Pygmies.

Altai Neanderthal admixture in Denisovans

This issue is not really explained in the paper as such, and we have to reach out to the Supplemental Information chapter 15 in order to grasp it.

It is clear that the Altai Neanderthals are closer to Denisovans than other Neanderthals are by approx. the following fractions (directly deduced from the raw affinities listed in fig. S6a.2):

  • 2% more than Mezhmaiskaya
  • 7% more than Vindija (avg.)
  • 9% more than El Sidrón
Feldhofer appears closer instead but this sequence was not used by the authors in most tests because it has too dubious quality.

In section 15 of the supplementary material, using complex methodology and lamenting the lack of a second Denisovan sample which would be most useful, they estimate a minimal 0.5% (Altai) Neanderthal introgression in Denisovans, with strong warnings that this could well be quite higher. I don’t know why they are not even considering a more direct approach, but I would dare to guesstimate the introgression to be close to 8% from the above raw data, assuming that there are no further complexities at play, such as other Heidelbergensis introgression in European Neanderthals, etc. The drift parameter (see above) does not seem to be one such complexity because Mezhmaiskaya is almost as drifted as Vindija yet it is consistently much closer, as it seems to correspond to its specific relatedness to Altai Neanderthals in mtDNA (and possibly also in nDNA if it is admixture what causes their pseudo-tree positioning closer to the root, what would be typical).

Note in blue is mine.

Mystery archaic genetic flow into Denisovans

The authors find that some 0.5-8% of the Denisovan genome appears to come from another hominin, which split from the human trunk even earlier.

We caution that these analyses make several simplifying assumptions. Despite these limitations, we show that the Denisova genome harbors a component that derives from a population that lived before the separation of Neanderthals, Denisovans and modern humans. This component may be present due to gene flow, or to a more complex population history such as ancient population structure maintaining a larger proportion of ancestral alleles in the ancestors of Denisovans over hundreds of thousands of years.

Later in the discussion section they ponder further the implications of this finding:

The evidence suggestive of gene flow into Denisovans from an unknown hominin is interesting. The estimated age of 0.9 to 4 million years for the population split of this unknown hominin from the modern human lineage is compatible with a model where this unknown hominin contributed its mtDNA to Denisovans since the Denisovan mtDNA diverged from the mtDNA of the other hominins about 0.7–1.3 million years ago41. The estimated population split time is also compatible with the possibility that this unknown hominin was what is known from the fossil record as Homo erectus. This group started to spread out of Africa around 1.8 million years ago42, but Asian and African H. erectus populations may have become finally separated only about one million years ago43. However, further work is necessary to establish if and how this gene flow event occurred.

Going to the detail of the matter (i.e. supplemental material sections 16a and 16b), one of the key details is that present-day Africans share more derived alleles with Neanderthals than with Denisovans. This can only be explained because Denisovans have other archaic ancestry prior to their apparent divergence from Neanderthals or (what is about the same) because Denisovans diverged themselves prior to the Neanderthal-Sapiens split, what is what the mtDNA (unlike the nDNA) suggests. However the difference, even if consistent across comparisons, is too small (a few percentage points) to be attributed to the later scenario.

This means that Denisovans appear to be at nDNA level some sort of an independent branch of proto-Neanderthals with some other but minor archaic admixture. Instead at mtDNA level they appear to be unrelated to Neanderthals and related instead to H. heidelbergensis (a detail not discussed in this paper because it is a too recent independent discovery).

There are still many details to explore but, in principle, it would seem that the Denisovan branch appears to be a divergent proto-Neanderthal one (maybe related to the Hathnora hominin, which looks very much Neanderthal) with lesser other archaic (H. heidelbergensis?) admixture, which nevertheless remained prominent in their mtDNA for whatever accidental reason.

Whether the H. heidelbergensis population of Atapuerca responds to this same profile (i.e. they were Denisovans too) or belongs instead to the “other archaic” population which introgressed in the Denisovan genome remains to be solved. So far we only know the mitochondrial lineage and this one may be misleading, as seems to be the case with the Denisova hominin.

Note in red is mine

Modern human genetic evolution

Benefiting from the high quality of the archaic genomes of Altai, the authors cataloged a long list of simple mutations exclusive to our species: 31,389 single nucleotide substitutions and 4,113 short insertions and deletions (indels). Additionally they found other 105,757 substitutions and 3,900 indels shared by 90% of their modern human sample of 1094 individuals.

They suggest some lines for future research in this regard, maybe focusing on genes known to influence brain development or regions that could show signs of positive selection. These preliminary lines of research are explored in SI-20, noticing potential selection in genes that affect the ventricular zone of the brain and cell proliferation in fetal brain development.


A western riverine route for human migration to North Africa in the Abbassia Pluvial

Interesting study on paleo-rivers of the Sahara providing insight for a likely route for Homo sapiens to cross the Sahara towards NW Africa.
Tom J. Coulthard et al., Were Rivers Flowing across the Sahara During the Last Interglacial? Implications for Human Migration through Africa. PLoS ONE 2013. Open accessLINK [doi:10.1371/journal.pone.0074834]


Human migration north through Africa is contentious. This paper uses a novel palaeohydrological and hydraulic modelling approach to test the hypothesis that under wetter climates c.100,000 years ago major river systems ran north across the Sahara to the Mediterranean, creating viable migration routes. We confirm that three of these now buried palaeo river systems could have been active at the key time of human migration across the Sahara. Unexpectedly, it is the most western of these three rivers, the Irharhar river, that represents the most likely route for human migration. The Irharhar river flows directly south to north, uniquely linking the mountain areas experiencing monsoon climates at these times to temperate Mediterranean environments where food and resources would have been abundant. The findings have major implications for our understanding of how humans migrated north through Africa, for the first time providing a quantitative perspective on the probabilities that these routes were viable for human habitation at these times.

Figure 2. Simulated probability of surface water during the last interglacial.
figure details Archaeological sites, and an annual probability that a
location has surface water. The archaeological data are derived from a
number of sources (including [42], [66], [67], [68].
The findspots are characterised by Aterian and Middle Stone Age
artefacts such as bifacial foliates and stemmed Aterian points and/or
typical ‘Mousterian’ points, side scrapers and Levallois technology.
Most are represented by surface scatters but where stratified examples
exist these can be shown by dating (OSL and U-series techniques) and
geomorphological setting to belong within MIS 5e [41], [42].

As discussed in other occasions, it seems likely that some genetic remnants of those early migrations are still visible in at least some NW Africans.

See also:


Homo sapiens was in China before 100,000 years ago!

This finding consolidates the recent dating of African-like industries of India to c. 96,000 years ago, as well as other previous discoveries from mostly China, and, jointly, they totally out-date not just the ridiculous “60 Ka ago” mantra for the migration out-of-Africa (which we know is dated to c. 125,000 years ago in Arabia and Palestine) but also the previous estimates of c. 80,000 years ago for India (Petraglia 2007).
Guanjung Shen et al., Mass spectrometric U-series dating of Huanglong Cave in Hubei Province, central China: Evidence for early presence of modern humans in eastern Asia. Journal of Human Evolution, 2013. Freely accessible at the time of writing thisLINK [doi:10.1016/j.jhevol.2013.05.002]


Most researchers believe that anatomically modern humans (AMH) first appeared in Africa 160-190 ka ago, and would not have reached eastern Asia until ∼50 ka ago. However, the credibility of these scenarios might have been compromised by a largely inaccurate and compressed chronological framework previously established for hominin fossils found in China. Recently there has been a growing body of evidence indicating the possible presence of AMH in eastern Asia ca. 100 ka ago or even earlier. Here we report high-precision mass spectrometric U-series dating of intercalated flowstone samples from Huanglong Cave, a recently discovered Late Pleistocene hominin site in northern Hubei Province, central China. Systematic excavations there have led to the in situ discovery of seven hominin teeth and dozens of stone and bone artifacts. The U-series dates on localized thin flowstone formations bracket the hominin specimens between 81 and 101 ka, currently the most narrow time span for all AMH beyond 45 ka in China, if the assignment of the hominin teeth to modern Homo sapiens holds. Alternatively this study provides further evidence for the early presence of an AMH morphology in China, through either independent evolution of local archaic populations or their assimilation with incoming AMH. Along with recent dating results for hominin samples from Homo erectus to AMH, a new extended and continuous timeline for Chinese hominin fossils is taking shape, which warrants a reconstruction of human evolution, especially the origins of modern humans in eastern Asia.

The range of dates for the teeth is ample but the oldest one is of 102.1 ± 0.9 Ka ago. Other dates are very close to this one: 99.5 ± 2.2, 99.3 ± 1.6, 96.8 ± 1.0, etc. (see table 1), so there can be little doubt about their accuracy. 
The Huanglong teeth (various views)
Now, how solidly can these teeth be considered to belong to the species Homo sapiens? Very solidly it seems:

The seven hominin teeth from Huanglong Cave have been assigned to AMH
mainly because of their generally more advanced morphology than that of H. erectus and other archaic populations (Liu et al., 2010b),
especially in terms of the crown breath/length index. These teeth also
lack major archaic suprastructural characteristics listed by Bermúdez de Castro (1988)
for eastern Asian mid-Pleistocene hominins, such as “strong tuberculum
linguale (incisors), marked lingual inclination of the buccal face
(incisors and canines), buccal cingulum (canines and molars), wrinkling
(molars), taurodontism (molars), swelling of the buccal faces (molars)”
(Tim Compton, Personal communication). However, in their roots, these
teeth still retain a few archaic features, being more robust and
complicated than those of modern humans (Liu et al., 2010b).

Zhirendong jaw
Let’s not forget that further South in China, in Zhirendong, a “modern” jaw was found and dated to c. 100,000 years ago as well.
As for the so-called “molecular clock”:

The new timeline for human evolution in China is in disagreement with
the molecular clock that posits a late appearance for AMH in eastern
Asia (e.g., Chu et al., 1998).

… too bad for the “clock”, because a clock that doesn’t inform us of time with at least some accuracy is totally useless.

Echoes from the past (August-28-2013)

Oh, yeah, I admit it: I have been procrastinating a lot. Result: an extremely long “to do” list. Naturally, I can’t make up for all the past laziness, so here goes a synthesis of what would otherwise be left unattended, take your time, please. 
Middle Paleolithic:
Atapuerca holds “uninterrupted” sequence of European humans since 1.2 million years ago. Soon-to-be-published theory of continuity from H. erectus to Neanderthals in the Castilian site → Paleorama[es], EFE Futuro[es].
More Neanderthal evidence for symbolism found in Fumane cave (Veneto, Italy): polished and ochre-painted shells (pictured) → PLoS ONE (open access), El neandertal tonto ¡qué timo![es].
Upper Paleolithic:
Epigravettian burial, dated to ~14,000 BP, found in Cuges-les-Pins (Provence). The Epigravettian (and not the more widespread Magdalenian) culture of this site indicates a direct link to Italy → INRAP[fr], La Provence[fr], Los Andes[es].
Oldest modern human remain of Galicia found at Valdavara cave (Becerreá, Lugo province). The milk tooth is 17,000 years old, 7000 years older than any other such finding in the NW Iberian country → Pileta[es], IPHES[cat].
Thousands of engravings, dated to c. 6000 years ago, found in Coahuila (Mexico) → RTVE[es].
“World’s oldest calendar” found in Scotland → BBC.
Female burial found at Poças de São Bento (Sado basin, Portugal) → Paleorama[es].
First farmers were inbred (at least in Southern Jordan) → Science Magazine.
Qatar Neolithic dig shows the peninsula was in contact with early Sumerian civilization (Eridu or Ubaid period, the first empire ever) → The Archaeology News Network.
Manure was already used by Europe’s first farmers → Science.
Haryana (India) town is oldest large IVC settlement → Business Standard.
East China engravings show first Oriental writing (~5000 years’ old, just slightly younger aged as Sumerian cuneiform writing but much more recent than the controversial Tărtăria tablets of Bulgaria) → The Guardian, English People.
North American natives caused lead pollution in Lake Michigan (oldest recorded) → PPV paper (ER&T)University of Pittsburg.
Perdigões enclosure and collective burial was pilgrimage center. Antonio Valera (often so scholarly cryptic at his blog) loosens up when interviewed by a Portuguese publication, giving meaning to the archeology he’s working with → Super Interesante[por].
Bronze Age:
Cypriot harbor city dug: Hala Sultan Tekke, near modern Larnaka, had 25-50 Ha. and was active between the 16th and 12th centuries BCE → The Archaeology News Network.

Also from Cyprus: large settlement dug out near Nicosia (Cyprus), dated to 2000-1500 BCE → The Archaeology News Network.
Human evolution:
Modern human shoulder much more efficient than chimpanzees’ at throwing… but also than H. erectus’ → BBC.
Neanderthals did speak (of course) → Science Daily, open access paper (Frontiers in Psychology).

Note: their unfounded insistence on most unlikely H. heidelbergensis shared origins of Neanderthals and us casts some doubt on elements of their reasoning however.

Record ancient DNA: ~700,000 years’ old horse sequenced → Nature Communications (PPV).
Experimental archaeology:
How to carve your own stone tools and weapons out of modern materials: very interesting videos (in English) at Paleorama[es] (scroll down). 
More tomorrow (nope my “to do” list is not at all finished with this entry).

South Arabian paleolake Mundafan was inhabited in the Middle Paleolithic and later in the Neolithic

Another study also by Cressard researches two greatly different periods of occupation of what was once a lake in Southern Saudi Arabia, not far from Yemen.
Rémy Cressard et al., Middle Palaeolithic and Neolithic Occupations around Mundafan Palaeolake, Saudi Arabia: Implications for Climate Change and Human Dispersals. PLoS ONE 2013. Open accessLINK [doi:10.1371/journal.pone.0069665]


The Arabian Peninsula is a key region for understanding climate change and human occupation history in a marginal environment. The Mundafan palaeolake is situated in southern Saudi Arabia, in the Rub’ al-Khali (the ‘Empty Quarter’), the world’s largest sand desert. Here we report the first discoveries of Middle Palaeolithic and Neolithic archaeological sites in association with the palaeolake. We associate the human occupations with new geochronological data, and suggest the archaeological sites date to the wet periods of Marine Isotope Stage 5 and the Early Holocene. The archaeological sites indicate that humans repeatedly penetrated the ameliorated environments of the Rub’ al-Khali. The sites probably represent short-term occupations, with the Neolithic sites focused on hunting, as indicated by points and weaponry. Middle Palaeolithic assemblages at Mundafan support a lacustrine adaptive focus in Arabia. Provenancing of obsidian artifacts indicates that Neolithic groups at Mundafan had a wide wandering range, with transport of artifacts from distant sources.

Figure 5. General views of the Mundafan palaeolake.
Again the content is rich in details of great interest for the archaeologist and prehistorian but surely a bit harder to digest for the casual aficionado.
Of interest anyhow is that no Nubian Complex affinities have been observed in the Middle Paleolithic tools and cores, suggesting again that the colonization of Arabia and Palestine from Africa was multifaceted, with different and sometimes ill-defined cultural sources.
As for the Neolithic a problem is that in this and other sites, all findings are located on the surface, being therefore impossible to date stratigraphically. The kind of tanged arrowheads suggests, by comparison with other sites, that these findings belong to the oldest Neolithic phase, c. 8000-6000 calBP. There are no findings that could be attributed to later periods, probably because the area became just too dry. Interestingly:

The Mundafan Neolithic sites do not appear to be sedentary locations on the basis of the absence of architectural features, grindstones, domesticated faunal remains, and relatively low artifact densities. The prevalence of projectiles and other weaponry is probable evidence of hunting activities. Mundafan would have been a favorable setting for short-term hunting along the lakeshore. The presence of rare obsidian artifacts demonstrates Mundafan’s participation in long-distance mobility systems that included relations with the obsidian-rich mountainous zones of Yemen, some 400–500 km away from the site.

While the term “Neolithic” is used in the paper, the kind of economy that the people living there had seems to have been hunter-gatherer.
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Posted by on August 1, 2013 in Arabia, Middle Paleolithic, Neolithic, West Asia