Friday, November 29, 2024

A new alphabetic system was apparently discovered in north Syria.

A Newly Discovered Alphabetic System in Northern Syria

A new alphabetic writing system has apparently been discovered in northern Syria. It may represent the oldest known alphabet, dated to around 2400 BCE.

Until now, it was generally assumed that the first alphabet developed from Egyptian hieroglyphs, with later modifications appearing in Sinai and spreading from there to the Levant and Phoenicia.

However, this newly discovered script from ancient Syria appears to be older than the Proto-Sinaitic alphabet. If confirmed, this finding could significantly change our understanding of how and when alphabetic writing systems first emerged and evolved.

Wednesday, November 27, 2024

A Map Explaining the Formation of Modern Armenian Genetics

A Map Explaining the Formation of Modern Armenian Genetics

I created this map to illustrate how modern Armenian genetics formed. The map represents the genetic situation during the Middle Bronze Age, roughly 4,000 years ago. I deliberately chose these colors to emphasize the clinal nature of the genetic landscape.

The yellow area represents the Trialeti–Vanadzor / Lchashen cultural sphere, which shows high levels of steppe ancestry. In this context, these populations are usually associated with Etiuni.

The orange region has lower steppe ancestry, approximately comparable to that of modern Armenians. We have a few samples from this zone, including Van–Urartu.

The red region shows little or no steppe ancestry and instead has a stronger affinity to Levantine Bronze Age populations. It is notable that these areas were historically inhabited by Hurrians. We have some samples from Şırnak and Batman, although they are not recent enough to fully represent the situation during the Middle and Late Bronze Age. The Dinkha Tepe 2 sample dates to the Middle Bronze Age, but it comes from northwestern Iran, so it is not exactly representative of the red zone.

Further south, the Levantine lowlands were inhabited by populations genetically similar to the red region, but with a more pronounced southern shift. Numerous samples from sites such as Alalakh and Ebla illustrate this pattern.

Modern Armenians derive ancestry from all three regions—orange, yellow, and red. For most Armenians, the largest contribution comes from the orange region. Eastern Armenians show additional ancestry from the yellow zone, while Armenians from southwestern regions have significant orange ancestry but also some contribution from the red zone.

An important point to understand is that the orange region itself can be modeled as a mixture of yellow and red. In theory, this would allow us to reduce the number of colors used in the model, but doing so risks oversimplifying the situation. In practice, some alleles typical of the red region appear among eastern Armenians, while Armenians from southern and western areas also carry some alleles associated with the yellow region. Overall, these overlapping contributions cause all Armenian groups to cluster closely together on PCA plots.

Another key point is that modern Armenians do not show any significant additional ancestry from outside these colored regions. Of course, some sporadic influences occurred during later historical periods, but these are generally negligible and can usually be ignored in population-level calculations. Armenians who settled outside these regions sometimes acquired local ancestry, but such cases are historically documented and can be easily identified.

A reasonable question arises: why are samples from these three regions not directly used to model Armenians?

The issue likely relates to how modeling tools operate. When very closely related populations are used as sources, the standard errors increase, whereas using more distant populations often reduces them. Despite some exaggerated perceptions, the populations represented by these three colors are actually quite close genetically. For this reason, it can sometimes be easier to choose a more distant source from south of the red zone and obtain statistically feasible models. There may also be other technical factors involved that I am not fully aware of.

However, the real issue is not the models themselves. For example, Lazaridis also used Levant_N as a distal source and argued that its contribution increased after 600 BCE, yet this did not lead to sensationalist interpretations in the media. The real problem is the lack of historical interpretation accompanying many genetic models. When genetic results are not interpreted in the context of known historical processes, it is unsurprising that others interpret them according to their own narratives.

In this case, the relevant historical events are well known. One is the existence of a Hurrian cultural belt across the southern regions of historic Armenia, which likely had a more southern genetic profile. Another is the formation and expansion of the Urartian Empire. These two factors alone are sufficient to explain the main features of the modern Armenian genetic profile, although other events may also have played a role.

Hopefully, our paper with Armen Petrosyan will soon be published in English. In it, we discuss this period of genetic shift in eastern Armenia, and I hope it will help those who want to better understand this complex historical process.

PS below in the comments You can see a model mixing yellow and orange with high standard errors. Made by Nareg Asatrian


Tuesday, November 26, 2024

Sasun Armenians in Hovhannisyan et al. (2024)

 

Sasun Armenians in Hovhannisyan et al. (2024)

Hovhannisyan et al. (2024) published, for the first time, five genome-wide DNA samples of Sasun Armenians. Until now, we only had Y-DNA studies of Sasun Armenians, which showed that their Y-DNA pool differs somewhat from that of other Armenian subgroups (see picture 2). Various theories have been proposed to explain this difference based on historical records and local traditions.

The new paper examined this issue and found little difference between the autosomes of Sasun Armenians and other Armenian subgroups. This can be seen on the PCA, where Sasun samples plot close to other Armenians marked as E, W, and C, while Sasun is marked as S. All five Sasun samples fall on the southern side of the Armenian cluster, which corresponds well with their geographic location.

When the G25 coordinates of these samples become available, we will be able to examine them more closely.

Y-DNA Peculiarities

Understanding the distinct Y-DNA composition of Sasun Armenians will be difficult without ancient DNA from the region.

The haplogroup T likely had a homeland near or overlapping with the Sasun region. Meanwhile, the presence of R2 in Sasun may reflect a founder effect. Haplogroup R2 was prominent among Zagros Neolithic farmers and has recently also been identified among South Caucasus Neolithic populations.

Historical Context

The Y-DNA profile of Sasun may also be connected with the specific historical background of the region.

Assyrian sources mention a kingdom called Shubria in this area. The name of this kingdom derives from the older Sumerian term Subir. Very little is known about the Subir people, but later sources use the term Subarean language to refer to a Hurrian language. In the Iron Age, several Hurrian royal names are attested in this region. However, this does not necessarily mean that the earlier Subir populations were Hurrian as well.

The southern lowlands of Sasun had a Semitic presence, while in the north, in the Mush region, the Urumu tribes are attested. The Urumu, later known as Urme, were almost certainly an Armenian-speaking tribe.

Around 400 BCE, Xenophon described the Centrites River (modern Botan River) as the southern boundary of Armenian territory. Sasun lies north of this river, placing it clearly within the Armenian satrapy.

Conclusion

To fully understand the complex genetic history of Sasun and its surrounding regions, additional ancient DNA samples will be necessary




Sunday, November 24, 2024

The Distribution of EHG Ancestry Today

The Distribution of EHG Ancestry Today

The Eastern Hunter-Gatherer (EHG) genetic profile appears in Eastern Europe after the Last Glacial Maximum (around 20,000 years before present). Before that time, the region was inhabited by different populations that apparently disappeared due to extremely cold climatic conditions.

EHG samples are found across a wide geographic area, ranging from the North Caucasus to Karelia in the far north of Eastern Europe. Various maps on the internet attempt to illustrate the global distribution of EHG ancestry today. However, these maps require some clarification (see the link in the comment section).

Two Ways to Measure EHG Ancestry

There are two main ways to estimate the amount of EHG ancestry remaining in modern populations.

The first approach ignores the fact that much of the EHG ancestry was dispersed through the expansions of Yamnaya and Corded Ware populations. This method is commonly used, but it can be misleading. Because EHG constituted roughly half of the Yamnaya genetic profile, people may mistakenly assume that higher EHG levels automatically imply greater Yamnaya ancestry, which is not necessarily correct.

The second approach attempts to separate Yamnaya and Corded Ware ancestry from the total EHG signal, in order to identify the amount of “pure” EHG ancestry that remained independent of those migrations.

Modeling Method

To do this, I selected Corded Ware samples as a source population, since Yamnaya itself never moved into northern Europe—only Corded Ware groups derived from Yamnaya did.

I also included Ancient North Eurasian (ANE) samples from Siberia in order to avoid a pseudo-EHG signal, and used Karelia hunter-gatherers as a reference for pure EHG.

All modern populations were included in the analysis.

Results: Pure EHG

The highest levels of pure EHG ancestry not associated with Yamnaya migrations are found among:

  • Mari

  • Chuvash (a Turkic-speaking group)

  • Saami

  • some northern Russians

  • Udmurts

The highest value reaches about 33%, but most of these populations have less than 25%.

This indicates that relatively little pure EHG ancestry survives today outside the context of Yamnaya or Corded Ware expansions. It is mostly preserved in northeastern Europe, which makes sense because Corded Ware pastoralists never settled extensively in that region. The harsh climate likely made herding and early agriculture difficult, limiting their expansion there.

Corded Ware / Yamnaya Ancestry

The second chart shows where Corded Ware ancestry is highest today.

The peak levels occur in northern Europe, particularly among Germanic-speaking populations in Scandinavia, reaching about 53%.

Using Yamnaya instead of Corded Ware as a source produces essentially the same pattern. In other words, Yamnaya-related ancestry is highest in northwestern Europe.

This has a simple explanation: northern Europe, especially Scandinavia, had relatively low population density in prehistoric times, whereas southern Europe, West Asia, and South Asia had much denser populations. Migrating groups therefore left a larger genetic impact in sparsely populated regions.

Linguistic Implications

What does this distribution suggest about the language spoken by the northern EHG populations?

Since the highest levels of pure EHG are found only among a subset of Uralic-speaking groups, it is unlikely that the northern EHG originally spoke a Uralic language.

Moreover, many eastern Uralic-speaking populations have little or no EHG ancestry, although they do possess Yamnaya-related ancestry. The defining genetic feature of eastern Uralic speakers in Europe is the presence of Siberian / Nganasan-related ancestry, while their most frequent Y-DNA haplogroup (N1) also originates from Siberia.

Conversely, these northern populations virtually lack Y-DNA lineages associated with EHG. Any R1a present among them derives from Corded Ware expansions, not from earlier hunter-gatherer populations.

Taken together, this evidence suggests that the language spoken by the northern EHG populations is now extinct.

The Uralic-speaking populations likely arrived from Siberia sometime after 1500 BCE, while Indo-European groups in northern Europe—such as Balto-Slavic and Germanic speakers—descend largely from Corded Ware populations that expanded into the region after 2800 BCE.



Saturday, November 23, 2024

Nine principal genetic profiles of Western Eurasians

Nine Principal Genetic Profiles of Western Eurasians

We frequently use these terms, so it is useful to understand what they refer to. Most of these genetic profiles appeared after the Last Glacial Maximum. Before the Glacial Maximum (approximately 20,000–26,000 years ago), Eurasia was inhabited by populations with different genetic profiles.

All of these genetic profiles ultimately share common origins and descend from a single ancestral population that has not yet been sampled in ancient DNA studies.


Wednesday, November 20, 2024

Çayönü and the Preservation of Early Neolithic Farmer Ancestry

 

Çayönü and the Preservation of Early Neolithic Farmer Ancestry

Çayönü is an early Neolithic site located northeast of Portasar / Göbekli Tepe.

In Lazaridis et al. (2024), ancient DNA from Çayönü was used to model the Neolithic farmers of Armenia. These models should be considered preliminary, since we still lack hunter-gatherer DNA from historic Armenia. Nevertheless, they provide a useful indication of what we might expect.

I wanted to examine where the ancestry of these Çayönü early farmers is best preserved today. For this purpose, I selected 16 ancestral components and used them to model modern populations around the world.

Unsurprisingly, ancestry related to Çayönü farmers is best preserved among modern populations originating from Mesopotamia and historic Armenia.

For comparison:

  • Natufian ancestry from the neighboring Levant is best preserved today among populations in Yemen and Saudi Arabia.

  • Anatolian Neolithic farmer ancestry is best preserved in Sardinia and southern Europe.

It should be noted that this method produces different results than a simple distance comparison between Çayönü samples and modern populations. A direct distance analysis would show large genetic distances because this ancestry has been diluted over time. Moreover, because Çayönü farmers are genetically close to Anatolian and Levantine Neolithic populations, individuals from those regions would appear artificially prioritized.

The method used here attempts to remove that shared ancestry in order to identify where the specific Çayönü-related component has had the greatest long-term impact.

The results are shown in the first chart, sorted from highest to lowest.

In my next post, I will apply the same method to EHG ancestry.



Monday, November 18, 2024

Hunters and Early Farmers of the Urfa Region

Hunters and Early Farmers of the Urfa Region

The megalithic constructions of Portasar / Göbekli Tepe are well known. Another site with even more impressive statues has been discovered nearby at Karahantepe. In 2021, another remarkable discovery was made at Sayburç (see the map for the locations of these sites).

At Sayburç, human reliefs dating to around 9000 BCE were carved into stone. These works were apparently created by the early farmers of West Asia and the Fertile Crescent.

It is becoming increasingly clear that the hunter-gatherer societies that developed agriculture and domesticated animals possessed surprisingly complex social organization. Without metal tools, they must have spent a considerable amount of time polishing stone and carving rock, which suggests significant planning, labor organization, and cultural development.

Ancient DNA from nearby sites such as Nevali Çori and Çayönü is now available. These populations do not show any unusual or “exotic” ancestry; rather, genetically they occupy an intermediate position between several neighboring groups:

  • Anatolian hunter-gatherers

  • Pre-Pottery Neolithic Levantine populations (Natufians)

  • Neolithic farmers from the South Caucasus and historic Armenia

On the PCA (see the fourth picture), these populations appear within the blue hexagon located between three red circles, illustrating their intermediate genetic position among these three major groups.