January 11, 2006

New India Y-chromosome paper

A new Y-chromosome study comes at the heels of the Sengupta paper. It does not appear to be in the PNAS site yet, but here is a story from National Geographic.
India Acquired Language, not Genes, From West

Most modern Indians descended from South Asians, not invading Central Asian steppe dwellers, a new genetic study reports. The Indian subcontinent may have acquired agricultural techniques and languages—but it absorbed few genes—from the west, said Vijendra Kashyap, director of India's National Institute of Biologicals in Noida.
Based on my readings so far, I believe that the Proto-Indo-Iranians and hence the ancestors of the first speakers of Indic speakers belonged primarily to haplogroups J2a and R1a1. Today, J2a is found approximately 4% of Hindus, and primarily in the upper castes where the signal of the founders of the caste system would be most evident.

R1a1 is found across the caste hierarchy and in tribals and is more diverse in tribals and lower castes than in the upper castes. I suspect though, that the lack of informative subclades of R1a1 may mask multiple origins. Most of it is doubtlessly pre-Indo-European and probably pre-Neolithic, but some yet-undetected clade will be discovered that is of more recent origin. This will reflect the genetic contribution of Eurasian steppe groups which were themselves Indo-Europeanized at an earlier time from J2a-bearing populations that spread from Anatolia through the Balkans into Eastern Europe.

So, Hindus are indeed primarily descended from Pre-Indo-European populations, but they may still possess the signal of the arrival of the first Indic speakers. This will become even clearer once informative SNPs are discovered in haplogroup R1a1.

More to follow once I get a copy of the paper.

January 10, 2006

Excavation on Keros aims to solve riddle of Cycladic figurines


From CBSNews (excerpt):
"What is particularly impressive is not just the bulk of the finds, which is larger than the total from the rest of the Cyclades, but also that they were intentionally broken during ancient times," Sotirakopoulou said. "Therefore, this is a very important, a unique site."

The Cycladic culture _ a network of small, sometimes fortified farming and fishing settlements that traded with mainland Greece, Crete and Asia Minor _ is best known for its elegant artwork: mostly naked, elongated figures with their arms folded under their chest. The seafaring civilization was eclipsed in the second millennium B.C. by Crete and Mycenaean Greece.

...

Evidence from excavations in the '60s and 1980s failed to explain why the barren islet was so much more important in the 3rd millennium B.C. than its bigger, more hospitable neighbors.

"The prevailing explanation is that this was a sacred repository, a sort of pan-Cycladic sanctuary where people left objects within the framework of rituals which included their intentional smashing," said Sotirakopoulou.

She will participate in the summer's excavation together with Cambridge University professor Colin Renfrew and other experts.

Early human population centers in coastal habitats (?)

I am skeptical whether this result is an artefact of the composition of the 51 populations, or whether it reflects prehistoric realities, but the paper is worth reading nonetheless.

Examples of 50%-confidence kernels for population placement based on population average allele frequencies. Populations are: Columbian, Hezhen, Kalash, Karitiana, Lahu, Makrani, Mandega, Maya, Mbuti Pigmy, Melanesian, Mozabite, New Guinea, Orcadian, Palestinian, Pima, Russian, Sardinian, Uygur, Yakut, Yizu, and San. In most cases, a single kernel results, although, in populations Hezhen, Karitiana, and Pima, the kernel has broken into two or three regions.

Proc. Natl. Acad. Sci. USA, 10.1073/pnas.0507991103

Global genetic positioning: Evidence for early human population centers in coastal habitats

William Amos and Andrea Manica

For an alternative perspective on relationships among human populations, we combined genetic and geographic information, using allele frequency gradients to place populations and individuals on the globe. Reanalyzing published data on 51 worldwide populations [Rosenberg, N. A., Pritchard, J. K., Weber, J. L., Cann, H. M., Kidd, K. K., Zhivitovsky, L. A. & Feldman, M. W. (2002) Science 298, 2381-2385] reveals five geographic clusters lying in plausible sites either of early agricultural innovation or on ancient migration routes. Also, the inferred sites show significant association with coastlines, suggesting that most early humans lived near large bodies of water. Our approach is flexible, and developments should prove useful both for exploring historical demography and for the identification of likely origin for unknown forensic samples.

Link

January 08, 2006

News from the J world

An M410 project, named after the M410 mutation defining haplogroup J2a, has been recently launched. It has a nice table of J2a frequencies from the recent Sengupta paper.

Also, a new J2 Y-DNA project was started. Unfortunately, project haplotypes are not listed, but you can at least get a basic introduction into haplogroup J2, with more statistical analyses to come. The site contains a nice graphic of the phylogenetic correspondences of the new and old nomenclatures, which seems to be on the whole accurate, although the left-most paragroup should be labeled J2*(xDYS413<=18,J2h) (9 Jan: fixed).

The M410 project hosts the very informative Y haplogroup J database (yJdb) that seems to contain nearly all major published haplotypes of haplogroup J, a very convenient resource for cataloguing and searching J haplotypes. I will add yJdb to my list of genetic databases on the right sidebar.

Both projects seem to support haplotype submissions from regular people. An interesting feature of the the yJdb system is that it allows users to enter SNP results, unlike the mainstram ysearch and ybase databases. This is quite useful when trying to compare haplogroup names across different nomenclature systems and with different sets of genotyped markers.

If you are aware of other worthwhile efforts, feel free to leave a comment.

January 06, 2006

Y chromosomes of Golla subcastes


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American Journal of Physical Anthropology (Early view)

Genetic diversity within a caste population of India as measured by Y-chromosome haplogroups and haplotypes: Subcastes of the Golla of Andhra Pradesh

R. John Mitchell et al.

Abstract

The extent of population subdivision based on 15 Y-chromosome polymorphisms was studied in seven subcastes of the Golla (Karnam, Pokanati, Erra, Doddi, Punugu, Puja, and Kurava), who inhabit the Chittoor district of southern Andhra Pradesh, India. These Golla subcastes are traditionally pastoralists, culturally homogeneous and endogamous. DNA samples from 146 Golla males were scored for seven unique event polymorphisms (UEPs) and eight microsatellites, permitting allocation of each into haplogroups and haplotypes, respectively. Genetic diversity (D) was high (range, 0.9048-0.9921), and most of the genetic variance (>91%) was explained by intrapopulation differences. Median-joining network analysis of microsatellite haplotypes demonstrated an absence of any structure according to subcaste affiliation. Superimposition of UEPs on this phylogeny, however, did create some distinct clusters, indicating congruence between haplotype and haplogroup phylogenies. Our results suggest many male ancestors for the Golla as well as for each of the subcastes. Genetic distances among the seven subcastes, based on autosomal markers (short tandem repeats and human leukocyte antigens) as well as those on the chromosome Y, indicate that the Kurava may not be a true subcaste of the Golla. Although this finding is based on a very small Kurava sample, it is in accordance with ethnohistorical accounts related by community elders. The Punugu was the first to hive off the main Golla group, and the most recently separated subcastes (Karnam, Erra, Doddi, and Pokanati) fissioned from the Puja. This phylogeny receives support from the analysis of autosomal microsatellites as well as HLA loci in the same samples. In particular, there is a significant correlation (r = 0.8569; P = 0.0097) between Y-chromosome- and autosomal STR-based distances.

Link

New reconstruction of Krapina 5 Neandertal

See also, The rituals of the Krapina Neandertals

American Journal of Physical Anthropology (Early view)

New reconstruction of Krapina 5, a male Neandertal cranial vault from Krapina, Croatia

Rachel Caspari, Jakov Radovi

Abstract

The Neandertals from Krapina, Croatia represent some of the geologically oldest Neandertals known, and they comprise the largest Neandertal collection from a single site in the world. However, comparisons of the Krapina material with other, later Neandertals have been limited both because of their fragmentary condition and because the sample has a disproportionate number of females and/or young individuals. This paper presents a preliminary description of our new reconstruction of Krapina 5, an adult male, and provides comparisons with females from Krapina and with later Neandertal males from Western Europe. Like other hominid sites with large samples, there is considerable cranial variation at Krapina; we believe that some, but clearly not all of it is due to sexual dimorphism. Although Krapina 5 differs from the later males in a number of features, such as cranial thickness, cranial height, and sagittal curvature, it fits well within the male Neandertal range for most other metric variables, including cranial capacity.

Link

Mozart's skull and the DNA of the famous

Scientists are tight-lipped about the genetic testing of the skull believed to be Mozart's. My bet is that it will be his skull. Resarchers have compared him with his maternal grandmother, so I predict that this will be an mtDNA-based study.

So, will Wolfgang Amadeus join the ranks of the famous past and present whose patrilineal or matrilineal haplogroup is recorded? So far we have Genghis Khan [Y: C*(xC3c)], Somerled [Y: R1a1], Thomas Jefferson [Y: K2], the Manchu dynast Nurhachi [Y: C3c] (*), the founder of the Uí Néill dynasty [Y: R1b], the Tyrolean Ice Man [K], Cheddar Man [mt: U5a], Tsar Nicolas [mt: T], Spencer Wells [Y: R1b], and of course none others than Matt Lauer [Y: J2], Katie Couric [mt: K], Ann Curry [mt: N9a], and Al Roker [Y: E*(xE3a) ?] of the Today Show.

Update

Well the "clear result" that the scientists advertised is actually this:
The scientists said on Austrian television Sunday that the skeletons do not match the skull, and that the skeletons are also unrelated - creating a whole new mystery of who is buried the Mozart family crypt.
(*) Whose fictional remains make a cameo in Indiana Jones and the Temple of Doom for those interested in movie trivia.

Update

See also Famous DNA.

Update

More here.

“I am quite disappointed that the mystery continues,” said Parsons. “All the samples from the three who were believed to be relatives of Mozart all had different mitochondrial DNA from each other, and from the Mozart skull. So if any one of them is an actual maternal relative of Mozart, it means that the skull is not Mozart’s. We don’t know if that is the case so the final analysis is inconclusive.

“We have attained definitive results from the skull,” said Parsons. “In the future, if anyone comes forward with an authentic matrilineal relative or a paternal relative, we now have ‘y’ chromosomal data and we will be in a position to make a confirmation. It’s considered to be known where Mozart’s sister Nannerl is buried, but I don’t know if there are any plans in Austria to act on that information and work another archeological exhumation.”

After several months of testing, the true identity of the skull remains inconclusive to be that of world-renowned 18th-century classical musical composer Mozart.

January 05, 2006

New dates for Vindija Neandertals: around 32-33kya

Proceedings of the National Academy of Sciences (published online)

Revised direct radiocarbon dating of the Vindija G1 Upper Paleolithic Neandertals

Tom Higham et al.

The 1998/1999 direct dating of two Neandertal specimens from level G1 of Vindija Cave in Croatia to approximately 28,000 and approximately 29,000 radiocarbon (14C) years ago has led to interpretations concerning the late survival of Neandertals in south-central Europe, patterns of interaction between Neandertals and in-dispersing early modern humans in Europe, and complex biocultural scenarios for the earlier phases of the Upper Paleolithic. Given improvements, particularly in sample pretreatment techniques for bone radiocarbon samples, especially ultrafiltration of collagen samples, these Vindija G1 Neandertal fossils are redated to approximately 32,000-33,000 14C years ago and possibly earlier. These results and the recent redating of a number of purportedly old modern human skeletal remains in Europe to younger time periods highlight the importance of fine chronological control when studying this biocultural time period and the tenuous nature of monolithic scenarios for the establishment of modern humans and earlier phases of the Upper Paleolithic in Europe.

Link

J variance in Iran, Pakistan, India, Turkey, and the Balkans

Quintana-Murci et al. reported that the STR variance in haplogroup J is
  • 0.57 in Iran
  • 0.47 in Pakistan
  • 0.36 in India
On the same loci, the STR variance derived from the Balkan data of Bosch et al. is 0.55. The Balkan data belong mainly to haplogroup J2. According to the data of Cinnioglu et al. on the same loci, the J variance is 0.63. Most Turkish samples belong to haplogroup J2 with a significant non-J2 minority. The composition of the Iranian J sample in terms of sub-haplogroups is unknown.

See also STR variance of haplogroup J2 in the Balkans and Anatolia.

Correlations of US height and body mass index

Journal of Biosocial Science (online early)

SPATIAL CORRELATES OF US HEIGHTS AND BODY MASS INDEXES, 2002

JOHN KOMLOS and BENJAMIN E. LAUDERDALE

Abstract

Aiming to further explore possible underlying causes of the recent remarkable stagnation and relative decline in American heights, this paper describes the result of analysis of the commercial US Sizing Survey (2002). Heights are correlated positively with income and education among both white males and females while Body Mass Index (BMI) is correlated negatively among females, as in other samples. In contrast to much of the literature, this paper considers geographic correlates of height such as local poverty rate, median income and population density at the zip code level of resolution. After adjusting for confounding factors that influence height such as income and education, population density is found to be strongly and negatively correlated with height among white men, but less so among white women. The effect on BMIs less convincing. Other ethnic groups are not analysed in detail because of the small number of observations available. Local economic conditions as measured by median income, unemployment and poverty rate do not have a strong correlation with height or BMI after adjusting for individual income and education.

Link

January 04, 2006

The prion protein gene in humans revisited

A few years ago, in a widely reported study, it was postulated that cannibalism may have been quite frequent in human evolutionary history. This conclusion was reached by the study of genes which protect people from brain-related diseases associated by cannibalism, similar to "mad cow disease". Now, a new study throws doubt on these earlier findings, showing that there was no rampant general cannibalism in the human past.

See also History of human cannibalism eats away at researchers.

Genome Res. 2005 Dec 20; [Epub ahead of print]

The prion protein gene in humans revisited: Lessons from a worldwide resequencing study.

Soldevila M, Andres AM, Ramirez-Soriano A, Marques-Bonet T, Calafell F, Navarro A, Bertranpetit J.

Ample evidence has accumulated showing that different coding variants of the PRNP gene confer differential susceptibility for prion diseases. Here we evaluate the patterns of nucleotide variation in PRNP exon 2, which includes all the protein-coding sequence, by resequencing a worldwide sample of 174 humans for 2378 bp. In line with previous studies, we found two main haplotypes differentiated by nonsynonymous substitution in codon 129. Our analyses reveal the worldwide pattern of variation at the PRNP gene to be inconsistent with neutral expectations, indicating instead an excess of low-frequency variants, a footprint of the action of either positive or purifying selection. A comparison of neutrality test statistics for PRNP with other human genes indicates that the signal of positive selection on PRNP is stronger than expected from a possible confounding genome-wide background signal of population expansion. Two main conclusions arise from our analysis. First, the existence of an ancient, stable, balanced polymorphism that has been claimed in a previous study and related to cannibalism can be rejected and is shown to be due to ascertainment bias. Second, our results are consistent with a complex history of selection including mainly positive selection, even if short local periods of balancing selection (Kuru-like episodes), or even a weak purifying selection model, are consistent with our data.

Link

STR variance of haplogroup J2 in the Balkans and Anatolia

I have calculated the STR variance of haplogroup J2 chromosomes in the Balkans, based on the recent study by Bosch et al. and in Anatolia, reported by Cinnioglu et al. Since Bosch et al. studied more microsatellites, and microsatellite mutation rates are variable, I have made the comparison based on the 10 microsatellites used by Cinnioglu et al. (DYS19 DYS388 DYS390 DYS391 DYS392 DYS393 DYS389I(CD) DYS389II(AB) DYS439 DYSA7.2). I have also adjusted the DYS389ii value reported by Bosch et al. to conform to the Cinnioglu et al. convention.

STR variance in J2 chromosomes in Turkey is 0.52, precisely as originally reported by Cinnioglu et al. The corresponding value for the Balkan populations sampled by Bosch et al. is 0.56.

Please, also note that Bosch et al. report two haplotypes #145 and #166 that occur in 19 and 17 cases, and may represent a founder effect in specific populations.

The results of these two studies are broadly compatible with the observations of Malaspina et al. on STR variatiance within haplogroup J2a1.

Update

Behar et al. also report allele variances for Ashkenazi Jewish (0.28) and non-Jewish Europeans (0.37). They include the DYS426 locus instead of DYS461/DYS A7.2. Their European sample did not include Balkan populations, except for some Romanians.

Update 2

The STR variance of J2a in India is 0.34 (data from Sengupta 2006). The variance of J2b is 0.34.

Update 3

The variance of J2a in Turkey is 0.47. The variance of J2b is 0.24.

January 03, 2006

On Genetic Palimpsests

Most of the genetic markers used in human phylogeographic studies have been dated to the prehistoric period, and the majority of them are of Upper Paleolithic origin.

Lately, subclades identified within some human lineages on the Y-chromosome have crossed the Neolithic barrier, and in even rarer cases, "signatures" of historical events, such as the dominance of the Mongols, the Manchu, or the Ui Neill.

As a result, most markers are suitable for examining events of human prehistory, and not of historical ethnic groups.

Of course, scientists have tried to apply genetic information to historical processes, e.g., in the case of Jewish origins, but it turns out that the "Jewish gene" or Cohen Modal Haplotype actually turns out to to be much older and not particularly Jewish after all.

Even with old markers, it is still possible to reason about historical events. For example, the theories of white nationalist Arthur Kemp about the widespread prevalence of black African slavery in the classical world have been squarely defeated by the near-complete absence of Sub-Saharan African markers in the Italian and Balkan peninsulas. Similar theories propagated by Gustav Kossina and the Aryan-Nordic camp about the Northern European origin of the Indo-Europeans of India have similarly been defeated, since Indians completely lack haplogroup I chromosomes that are frequent in European Nordic populations.

So, even though the markers in question are very old (I is of Upper Paleolithic age), we can still reason historically with them.

Often, this historical reasoning can be shaky. For example, Spencer Wells has made tall claims about the Phoenicians, the Sea Peoples, and the Carthaginians in a National Geographic article which were based on the analysis of haplogroup J and E distribution in the Levant and North Africa.

For example, he found that there was little impact of Phoenicians on Carthage, but his conclusions are based on the paucity of haplogroup J in modern North African populations, who are a much broader-group than the socially and geographically constrained group of the ancient Carthaginians. Similar claims were made regarding the non-impact of the Sea Peoples in the Levant, but again, this is based on the similarity between coastal and non-coastal populations.
But, for all we know subdivisions of haplogroup J and other Near Eastern markers may differ between coastal and non-coastal populations, or perhaps, the Sea Peoples did initially affect the coastal peoples, but later their genes diffused into non-coastal populations, removing the distinctiveness of the two.

Let us take a further example of Sicily. The island of Sicily was colonized initially by farmers, and later by Greeks and Phoenicians. All three groups are believed to have contained some "Neolithic" markers, such as haplogroups J, E3b, and G, so any inferences about the relative contributions of the three groups are on very shaky ground.

For example, Semino et al. proposed that only 7% of Calabrian Y-chromosomes are of Greek with the assumption that J2a and E3b represent Anatolian and Greek lineages respectively. But, the frequency of E3b in modern Peloponnesians is not necessarily representative of its frequency in the very specific ancient city states and medieval Greek populations that colonized Southern Italy, and J2a may have arrived in Calabria either from Anatolia, e.g., during the Neolithic, or from Greece, during the age of colonization.

Things become even more complex when we turn to the Balkans or to Anatolia. For example, I playfully recounted some random facts about Phrygo-Armenians, but these hardly scratch the surface of the problem. Hittites, themselves either native or intrusive, were unseated by Phrygians, who were conquered by Persians, who were conquered by Macedonian Greeks, who were conquered by Romans, who were conquered by Turks. Not to mention the Galatians of Ancyra, or the ubuiquitous Armenians of the Byzantine Empire, or even the Jews of both the ancient and more recent origin, and of course the Turks themselves as well as imported Muslims from former provinces or vassals of the Ottoman Empire. And, of course, we should not forget that present-day Anatolians are only a subset of very recent Anatolians, several million of who were liquidated or deported following World War I.

These remarks underscore the near hopelessness of untangling historical patterns on the basis of phylogeography. Is there a way out?

Part of the solution will consist of performing huge studies with large sample sizes and very recently derived genetic markers, augmented by separate genome-wide autosomal clustering methods that may unmask latent genetic components that may be correlated with historical groups. Such studies will be very costly, even though the price of DNA testing is likely to go down, because ultimately the hard work of sample collection has to be done and paid for.

The ultimate solution, would be some significant progress in ancient DNA extraction. At present, mtDNA is the only game in town, and inferences from mtDNA are always up for grabs, due to the potential for contamination, uncertainties about selection, and of course the simple fact that ancient civilizations were largely patriarchal.

An even more exciting development would be the discovery -in modern human populations- of the genetics underlying common human variation in metric and morphological traits. Then, by examing ancient skeletal remains, we will be able to estimate the genetic identity of populations even if DNA cannot be directly observed.

The technical challenges are enormous, but -in my opinion- are not the main challenges at all. As hinted in Genetic vs. Mythical Origins, the study of the past forces us to question our ideas of descent and ethnicity. In the end, will it lead to an erosion of ethnic identity, or to its reinforcement along genetic and hence "objective" lines?

Looking forward to in 2006

I have already posted some of the highlights of the past year. Here are some of the things that I am looking forward to this year, partly inspired by John Hawks' oracles:
  • The first study on ancient Mycenaean and Minoan mtDNA.
  • A study on haplogroup E-M78 subdivisions.
  • A study on Minoan civilization origins.
  • Successful extraction of autosomal DNA from prehistoric humans.
  • Correlation of recently selected genes with IQ and/or personality.
  • Even more debate between demists and acculturationists regarding the spread of the Neolithic.
  • Even more debate between assimilationists and non-assimilationists about the Neandertals.
  • At least one paper from the Genographic project in a venue other than National Geographic about some obscure people that no one has heard about but everyone will talk about for days. The paper will have a feel-good message about the unity of mankind.
  • The French will continue to remain a genetic mystery, but there will be at least three more studies on Jewish population genetics.

January 02, 2006

Some aspects of J2 distribution

Haplogroup J2 consists exclusively of two separate subclades: J2a-M410 and J2b-M12.

Crete, occupying the southmost of the Greek world has an M12/M172 ratio of 2.2% [1]. This ratio is 20% [1] or 42.2% [2], a weighted average of 26%. In Northern Greece (Macedonia) it is 43.2% [2].

In Albania, the same ratio is 100% in the small sample of [1] and 54.6% as reported by [2], a weighted average of 55%.

In Bulgaria, the ratio is 28.6% [1] and in Romania, the ratio is 0% in the good sample of [1]. In the Ukraine it is 32.9% [2]

According to [3], the ratio is high in Serbs (66.3%). The few Croatians and Herzegovinians belonging in haplogroup J2 belong to the M12 clade, giving a ratio of 100% [2,3]. Similarly in Poland (100%) [2], and Czech Republic/Slovakia (50%) [1].

The distinction between the Western and Eastern Balkans that I have spoken of before is clear in this regard. M12 clade comprises the majority of J2 in the West and the minority in the East. Moreover, Slavic speakers of continental Europe belong more to the M12 clade, whereas those bordering Black Sea are more inclined to have a low frequency of M12, including the non-Slavic Romanians who lack M12 altogether. In historical times, the Balkans were inhabited by several Indo-European peoples which could be classified in the macro-groups of Illyrians (west) and Thracians (east). Greek trade and settlement occurred in both the Adriatic and the Black Sea, but the Greek presence was probably heavier and more long-lasting (until recent times) in the latter region.

Italy resembles the Greek-Black Sea area. Southern Italy has a ratio of 12.4%, while Northern Italy has a ratio of 25% [1]. North-Central Italy (35.7%), and two Calabrian samples (1%), and Sicily (0%). The latter two locations were Greek speaking for the major part of their recorded history.

Turkey resembles the Greek-Black Sea-South Italian area with an overall ratio of 7.1% [4]. Turkey was primarily Greek, Armenian and Kurdish speaking before the arrival of the Altaic-speaking Turks. Before that, it was also home to a variety of languages, including several extinct languages of the Indo-European family such as Hittite, Luvian, Palaic, Lydian, Lycian, Phrygian, and Celtic.

[1] Di Giacomo (2004)
[2] Semino (2004)
[3] Pericic (2006)
[4] Cinnioglu (2004)

Some random (?) facts


"The Phrygians had an equipment very like that of the Paphlagonians with some slight difference. Now the Phrygians, as the Macedonians say, used to be called Brigians during the time that they were natives of Europe and dwelt with the Macedonians; but after they had changed into Asia, with their country they changed also their name and were called Phrygians. The Armenians were armed just like the Phrygians, being settlers from the Phrygians. Of these two together the commander was Artochmes, who was married to a daughter of Dareios." Herodotus, vii, 73

"Phrygia is the Greek name of an ancient state in western-central Anatolia (modern Turkey), extending from the Eskishehir area east to (perhaps) Bogazköy and Alishar Hüyük within the Halys River bend. The Assyrians, a powerful state in northern Mesopotamia to the south, called the state Mushki; what its own people called it is unknown. We know from their inscriptions that the Phrygians spoke an Indo-European language. Judging from historical records supported by ceramic evidence, settlers migrating from the Balkans in Europe first settled here a hundred or more years following the destruction of the Hittite empire (ca. 1200 BC)." The Metropolitan Museum of Art: 'Phrygia, Gordion, and King Midas in the Late Eighth Century B.C.'

"There is evidence that in ancient times a distinct subfamily of Indo-European languages existed that is now called Thraco-Phrygian. To it belonged Phrygian (an ancient and now extinct Indo-European language of Anatolia) and Thracian (a now dead Indo-European tongue of the Balkans in antiquity). Modern Armenian may well be a direct descendant of Phrygian." The Columbia Encyclopedia: 'Armenian language'

"All the unrooted trees agree that there are four supergroups of IE languages (Balto-Slavonic, Romano-Germano-Celtic, Armenian-Greek, and Indo-Iranian)" Rexova K. (2003) Cladistic analysis of languages: Indo-European classification based on lexicostatistical data, Cladistics 19(2)

Interpolated map of haplogroup J2a frequency. Extracted from Sengupta et al. (in press).

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Ancient Phrygia, map extracted from Ancient Anatolia web site.

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