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Showing posts with label Middle East. Show all posts
Showing posts with label Middle East. Show all posts

Sunday, November 10, 2019

Etruscans, Latins, Romans and others


I've just added coordinates for more than 100 ancient genomes from the recently published Antonio et al. ancient Rome paper to the Global25 datasheets. Look for the population and individual codes listed here. Same links as always:

Global25 datasheet ancient scaled

Global25 pop averages ancient scaled

Global25 datasheet ancient

Global25 pop averages ancient

Thus far I've only managed to check a handful of the coordinates, so please let me know if you spot any issues. Below is a Principal Component Analysis (PCA) featuring the Etruscan and Italic speakers. I ran the PCA with an online tool specifically designed for Global25 coordinates freely available here.


Can we say anything useful about the origins of the Etruscan and early Italic populations thanks to these new genomes? Also, to reiterate my question from the last blog post, what are the genetic differences exactly between the Etruscans, early Latins, Romans and present-day Italians? Feel free to let me know in the comments below.

Update 13/11/2019: Here's another, similar PCA. This one, however, is based on genotype data, and it also highlights many more of the samples from the Antonio et al. paper. Considering these results, I'm tempted to say that the present-day Italian gene pool largely formed in the Iron Age, and that it was only augmented by population movements during later periods. The relevant datasheet is available here.


Update 13/11/2019: It seems to me that the two Latini-associated outliers show significant ancestry from the Levant, which possibly means that they're in part of Phoenician origin. These qpAdm models speak for themselves:

ITA_Ardea_Latini_IA_o
ITA_Proto-Villanovan 0.547±0.081
Levant_ISR_Ashkelon_IA2 0.453±0.081
chisq 7.573
tail prob 0.87027
Full output

ITA_Prenestini_tribe_IA_o
ITA_Proto-Villanovan 0.679±0.068
Levant_ISR_Ashkelon_IA2 0.321±0.068
chisq 7.222
tail prob 0.89033
Full output

The Proto-Villanovan singleton is also a key part of the models. Dating to the Bronze Age/Iron Age transition, she appears to be of western Balkan origin. Moreover, her steppe ancestry is probably derived directly from the Yamnaya horizon.

ITA_Proto-Villanovan
HRV_Vucedol 0.677±0.031
Yamnaya_RUS_Samara 0.323±0.031
chisq 10.397
tail prob 0.661174
Full output

The cluster made up of four early Italic speakers can be modeled with minor Proto-Villanovan-related ancestry, but, perhaps crucially, it doesn't need to be. Indeed, judging by the qpAdm output below, it's possible that almost all of its steppe ancestry came from the Bell Beaker complex, and, thus, the Corded Ware culture complex before that.

ITA_Italic_IA
Bell_Beaker_Mittelelbe-Saale 0.480±0.055
ITA_Grotta_Continenza_CA 0.411±0.042
ITA_Proto-Villanovan 0.109±0.084
chisq 10.294
tail prob 0.590205
Full output

Two out of the three available Etruscans look very similar to the Italic speakers in the above PCA plots, and yet they show a lot more Proto-Villanovan-related ancestry in my qpAdm run. The statistical fit is also relatively poor, perhaps suggesting that something important is missing.

ITA_Etruscan
Bell_Beaker_Mittelelbe-Saale 0.186±0.081
ITA_Grotta_Continenza_CA 0.283±0.064
ITA_Proto-Villanovan 0.531±0.126
chisq 17.175
tail prob 0.143143
Full output

Interestingly, the Etruscan outlier with significant North African admixture (proxied in my run by MAR_LN) doesn't need to be modeled with any Bell Beaker ancestry.

ITA_Etruscan_o
ITA_Proto-Villanovan 0.675±0.057
MAR_LN 0.325±0.057
chisq 14.864
tail prob 0.315912
Full output

Update 17/11/2019: The spatial maps below show how three groups of ancient Romans (from the Imperial, Late Antiquity and Medieval periods) compare to present-day West Eurasian populations in terms of their Global25 coordinates. The hotter the color, the higher the similarity. More here.




See also...

Getting the most out of the Global25

Thursday, November 7, 2019

What's the difference between ancient Romans and present-day Italians?


The first paper on the genomics of ancient Romans was finally published today at Science [LINK]. It's behind a paywall, but the supplementary info is freely available here. Below is a quick summary of the results courtesy of the accompanying Ancient Rome Data Explorer.



I'm told that the genotype data from the paper will be online within a day or so at the Pritchard Lab website here. I'll have a lot more to say about ancient Romans and present-day Italians after I get my hands on it.

See also...

Etruscans, Latins, Romans and others

Sunday, July 7, 2019

How did steppe ancestry spread into the Biblical-era Levant?


It's likely that at least two of the Philistines from Feldman et al. 2019 harbor relatively recent steppe ancestry. They're labeled ASH067 and ASH068 in the paper. The former individual is a male who belongs to Y-chromosome haplogroup R1, which appears to be R1b-M269 judging by the data from the relevant BAM file.

This is just the second instance of Y-haplogroup R1 from the pre-Crusades Levant, and, of course, neither R1 nor R1b-M269 appear in the Near Eastern ancient DNA record prior to the expansions of the Yamnaya and other closely related pastoralist groups from the steppes and forest steppes of Eastern Europe.

So how did the Yamnaya-related ancestry spread into the Biblical-era Levant? Did it come via Anatolia, the Caucasus and/or the Mediterranean?

To try and answer this question I analyzed separately the genome-wide data for ASH067 and ASH068 with qpAdm, relying on outgroup and reference populations that weren't featured in the qpAdm runs in the Feldman et al. paper. I also limited the analyses to what were in my view the most proximate two- and three-way solutions in terms of chronology and geography.

The models with the best statistical fits, each labeled with their "tail probs", are available in a zip file here. From my experience with qpAdm, I'd say that the most useful models generally show comparably high tail probs but low chisq values and standard errors. Please note also that I discarded all of the models with at least one standard error higher than 0.2 and/or based on less than 100K SNPs.

As far as I can see, these two are among the very best outcomes. Bell_Beaker_FRA are nine samples associated with the Bell Beaker culture (BBC) from what is now France. Interestingly, the BBC population was rich in Y-haplogroup R1b-M269.

Levant_ISR_Ashkelon_IA1_ASH067
Bell_Beaker_FRA 0.116±0.059
GRC_Minoan 0.507±0.111
Levant_ISR_Ashkelon_LBA 0.377±0.117
chisq 9.018
tail prob 0.530432

Levant_ISR_Ashkelon_IA1_ASH068
Bell_Beaker_FRA 0.237±0.044
GRC_Minoan 0.763±0.044
chisq 4.736
tail prob 0.943265

In my opinion, these models basically confirm that both ASH067 and ASH068 harbor Yamnaya-related ancestry. It's heavily diluted and minor, but it's there. Admittedly, even after looking over the qpAdm output several times, I'm still not quite sure how their ancestors acquired this ancestry. But for the time being, Mediterranean Europe appears to be the most plausible proximate source one way or another. Any thoughts about that? Feel free to share them in the comments below.

See also...

Evidence of European ancestry in the Philistines

R1b-M269 in the Bronze Age Levant

Late PIE ground zero now obvious; location of PIE homeland still uncertain, but...

Wednesday, July 3, 2019

Evidence of European ancestry in the Philistines


The abstract below has just appeared at the European Nucleotide Archive (see here), so I'm guessing that the relevant paper and accompanying ancient genome-wide data will be published within weeks if not days. Emphasis is mine:

The ancient Mediterranean port-city of Ashkelon, identified as “Philistine” during the Iron Age, underwent a dramatic cultural change between the Late Bronze- and the early Iron- Age. It has been long debated whether this change was driven by a substantial movement of people, possibly linked to a larger migration of the so-called “Sea Peoples”. Here, we report genome-wide data of ten Bronze- and Iron- Age individuals from Ashkelon. We find that the early Iron Age population was genetically distinct due to a European related admixture. Interestingly, this genetic signal is no longer detectible in the later Iron Age population. Our results support that a migration event occurred during the Bronze- to Iron- Age transition in Ashkelon but did not leave a long-lasting genetic signature.

Update 4/7/2019: The paper is now available at Science Advances [LINK]. One of the Ashkelon ancients, who also shows a relatively high level of European ancestry, belongs to Y-Chromosome haplogroup R1 (probably R1b-M269). I've updated my Global25 datasheets with the new samples. Look for the Levant_ISR_Ashkelon prefix. Same links as always...

Global25 datasheet ancient scaled

Global25 pop averages ancient scaled

Global25 datasheet ancient

Global25 pop averages ancient

This is how they cluster in my Principal Component Analysis (PCA) of ancient West Eurasian genetic variation. The relevant datasheet is available here. Based on these results, it's tempting to think that the European ancestry in the Philistines may have been of Greek provenance. But keep in mind that this is just a two dimensional view and a simplification of reality. I'll have more to say about the ancestry of these individuals and the origins of the Philistines in future blog posts.

See also...

Five foot Philistines

How did steppe ancestry spread into the Biblical-era Levant?

Monday, June 3, 2013

Recent gene flow from Africa and the Near East into Europe


A new paper at PNAS by Botigué et al. takes a close look at African and Near Eastern admixture in Europe:

Human genetic diversity in southern Europe is higher than in other regions of the continent. This difference has been attributed to postglacial expansions, the demic diffusion of agriculture from the Near East, and gene flow from Africa. Using SNP data from 2,099 individuals in 43 populations, we show that estimates of recent shared ancestry between Europe and Africa are substantially increased when gene flow from North Africans, rather than Sub-Saharan Africans, is considered. The gradient of North African ancestry accounts for previous observations of low levels of sharing with Sub-Saharan Africa and is independent of recent gene flow from the Near East. The source of genetic diversity in southern Europe has important biomedical implications; we find that most disease risk alleles from genome-wide association studies follow expected patterns of divergence between Europe and North Africa, with the principal exception of multiple sclerosis.

The term "recent" is used throughout the paper to describe the IBD results, but as far as I can see there's no mention of any dates. Based on the data in the very thorough Ralph and Coop European IBD study (see here), I'd say that segments of over 1.5cM represent gene flow from well within the past 5,000 years. If this assumption is correct, then the results certainly make a lot of sense. That's because there were well documented historical events that could account for the main outcomes in the figure below: a) low level IBD sharing between Sub-Saharan Africa and much of Southern Europe; b) inflated IBD sharing between North Africa and Southwestern Europe; and c) inflated IBD sharing between Southeastern Europe and the Near East.


I probably don't need to discus in detail what these events might have been. Suffice it to say that the Mediterranean Basin has seen several major empires which facilitated regular population movements between Southern Europe, North Africa and the Near East. This process included the slave trade, which was one of the main economic activities in the region for a couple thousand years.

It's important to note, however, that fastIBD doesn't specify the direction of gene flow. In other words, shared IBD segments can be the result of our ancestors either receiving or giving admixture, or gene flow from a third party. But as Botigué et al. point out, the North African samples which show the highest IBD sharing with Iberians are also those with the lowest European ancestry proportions in the ADMIXTURE analysis (see below). Therefore, it's unlikely that this shared IBD is of European origin in any significant degree.


Key: Canis - Canary Islands; And - Andalusia; Gal - Galicia; Bas - Basques; Spa - Spain; Por - Portugal; Fra - France; Ita - Italy; Tsi - Tuscany; Gre - Greece ; ItaJ - Italian Jews; AshJ - Ashkenazi Jews; Qat - Qatar; NMor - North Morocco; SMor - South Morocco; OccS - Saharawi; Alg - Algeria; Tun - Tunisia; Lib - Libya; Egy - Egypt; Yri - Yoruba from Nigeria; Mkk - Maasai from Kenya.


There's also a PCA in the supplementary PDF which further underlines that most of the IBD sharing between Europe and North Africa, as well as Qatar, is not of European origin, because it creates significant substructures within the European sample.


Unfortunately the Qataris are the only Near Eastern sample used in the study. Then again, if I was to pick a single ethnic group to represent the Near East in an IBD study like this, then Qataris would probably be near the top of the list. That's because they've been affected by population movements from other parts of the Arabian Peninsula and also Persia, but at the same time never experienced significant gene flow from Europe. More information about the genome-wide genetic ancestry of Qataris is available in this recent open-access paper by Omberg et al.

Botigué et al. also make some interesting comments about Jewish genetic ancestry in Europe. The quote below comes from the supplementary PDF.

Another possible hypothesis to explain the increased diversity in southern Europe is that an influx of Jewish ancestry had a heterogeneous effect on genetic diversity in Europe. However, in most European populations here, virtually no Jewish ancestry was detected. On average, 1% of Jewish ancestry is found in Tuscan HapMap population and Italian Swiss, as well as Greeks and Cypriots. This may reflect the higher sharing with Near Eastern populations in the Italian peninsula and southeastern Europe (Fig. 2C) or low levels of gene flow with the early Italian Jewish communities (6). Estimates from the IBD analysis are in agreement with ADMIXTURE estimates that the amount of sharing between these populations is extremely low (SI Appendix, Table S3). Specifically, results of IBD sharing between southwestern Europe and North Africa are two orders of magnitude greater than those found between the same region and Jews, the average WEA for southern Europe and North Africa is 203, while for southwestern Europe and European Jews is 1.3.

Reference...

LR Botigué*, BM Henn*, S Gravel, BK Maples, CR Gignoux, E Corona, G Atzmon, E Burns, H Ostrer, C Flores, J Bertranpetit, D Comas, CD Bustamante, Gene flow from North Africa contributes to differential human genetic diversity in Southern Europe, PNAS, published online before print June 3, 2013, doi: 10.1073/pnas.1306223110