Category: Culture

Paternal lineages mainly from migrants, maternal lineages mainly from local populations in Argentina

New paper (behind paywall) Genetic variation in populations from central Argentina based on mitochondrial and Y chromosome DNA evidence, by García, Pauro, Bailliet, Bravi & Demarchi, J. Hum. Genet (2018) 63: 493–507.

Abstract (emphasis mine):

We present new data and analysis on the genetic variation of contemporary inhabitants of central Argentina, including a total of 812 unrelated individuals from 20 populations. Our goal was to bring new elements for understanding micro-evolutionary and historical processes that generated the genetic diversity of the region, using molecular markers of uniparental inheritance (mitochondrial DNA and Y chromosome). Almost 76% of the individuals show

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Y-DNA haplogroup R1b-Z2103 in Proto-Indo-Iranians?

chalcolithic_early-asia

We already know that the Sintashta -Andronovo migrants will probably be dominated by Y-DNA R1a-Z93 lineages. However, I doubt it will be the only Y-DNA haplogroup found.

I said in my predictions for this year that there could not be much new genetic data to ascertain how Pre-Indo-Iranian survived the invasion, gradual replacement and founder effects that happened in terms of male haplogroups after the arrival of late Corded Ware migrants, and that we should probably have to rely on anthropological explanations for language continuity despite genetic replacement, as in the Basque case.

Nevertheless, since … Read the rest “Y-DNA haplogroup R1b-Z2103 in Proto-Indo-Iranians?”

Basal Eurasians split off ca. 80kya and contributed ca. 10% to EEF

3-population-moran-model

Efficiently inferring the demographic history of many populations with allele count data, by Kamm, Terhorst, Durbin, & Song (2018).

Abstract

The sample frequency spectrum (SFS), or histogram of allele counts, is an important summary statistic in evolutionary biology, and is often used to infer the history of population size changes, migrations, and other demographic events affecting a set of populations. The expected multipopulation SFS under a given demographic model can be efficiently computed when the populations in the model are related by a tree, scaling to hundreds of populations. Admixture, back-migration, and introgression are common natural processes that violate

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Agricultural origins on the Anatolian plateau

anatolia-neolithic-agriculture

New paper (behind paywall) Agricultural origins on the Anatolian plateau, by Baird et al. PNAS (2018), published ahead of print (March 19).

Abstract (emphasis mine):

This paper explores the explanations for, and consequences of, the early appearance of food production outside the Fertile Crescent of Southwest Asia, where it originated in the 10th/9th millennia cal BC. We present evidence that cultivation appeared in Central Anatolia through adoption by indigenous foragers in the mid ninth millennium cal BC, but also demonstrate that uptake was not uniform, and that some communities chose to actively disregard cultivation. Adoption of cultivation

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Differing modes of animal exploitation in North Pontic Eneolithic and Bronze Age Societies

north-pontic-eneolithic

Open access Differing modes of animal exploitation in North-Pontic Eneolithic and Bronze Age Societies, by Mileto, Kaiser, Rassamakin, Whelton & Evershed, STAR (2018). You can download the PDF.

Abstract (emphasis mine)

This paper presents new results of an interdisciplinary investigation of the diet and subsistence strategies of populations living in the North-Pontic region during the Eneolithic and the Early Bronze Age (ca. 3800 BC to the 2500 BC). New organic residue analyses of 200 sherds from five Eneolithic sites and two Early Bronze Age settlements are presented. The molecular and stable isotope results are discussed in relation to

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The time and place of European admixture in Ashkenazi Jewish history

Open access The time and place of European admixture in Ashkenazi Jewish history, by Xue, Lencz, Darvasi, Pe’er, & Carmi, PLOS Genetics (2018).

Abstract (emphasis mine):

The Ashkenazi Jewish (AJ) population is important in genetics due to its high rate of Mendelian disorders. AJ appeared in Europe in the 10th century, and their ancestry is thought to comprise European (EU) and Middle-Eastern (ME) components. However, both the time and place of admixture are subject to debate. Here, we attempt to characterize the AJ admixture history using a careful application of new and existing methods on a large AJ sample.

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Oldest N1c1a1a-L392 samples and Siberian ancestry in Bronze Age Fennoscandia

Open access preprint at bioRxiv, Ancient Fennoscandian genomes reveal origin and spread of Siberian ancestry in Europe, by Lamnidis et al. (2018).

Abstract (emphasis mine):

European history has been shaped by migrations of people, and their subsequent admixture. Recently, evidence from ancient DNA has brought new insights into migration events that could be linked to the advent of agriculture, and possibly to the spread of Indo-European languages. However, little is known so far about the ancient population history of north-eastern Europe, in particular about populations speaking Uralic languages, such as Finns and Saami. Here we analyse ancient genomic data

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Reconstructing the genetic history of late Neanderthals

neanderthal-late-europe

New paper (behind paywall) Reconstructing the genetic history of late Neanderthals, by Mateja Hajdinjak, Qiaomei Fu, Alexander Hübner, et al. Nature (2018).

Abstract (edited):

Although it has previously been shown that Neanderthals contributed DNA to modern humans, not much is known about the genetic diversity of Neanderthals or the relationship between late Neanderthal populations at the time at which their last interactions with early modern humans occurred and before they eventually disappeared. Our ability to retrieve DNA from a larger number of Neanderthal individuals has been limited by poor preservation of endogenous DNA and contamination of Neanderthal skeletal remains

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Yet another Bayesian phylogenetic tree – now for Dravidian

dravidian-languages

Open access A Bayesian phylogenetic study of the Dravidian language family, by Kolipakam et al. (including Bouckaert and Gray), Royal Society Open Science (2018).

Abstract (emphasis mine):

The Dravidian language family consists of about 80 varieties (Hammarström H. 2016 Glottolog 2.7) spoken by 220 million people across southern and central India and surrounding countries (Steever SB. 1998 In The Dravidian languages (ed. SB Steever), pp. 1–39: 1). Neither the geographical origin of the Dravidian language homeland nor its exact dispersal through time are known. The history of these languages is crucial for understanding prehistory in Eurasia, because despite their

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