There have been some disparate rightists who have claimed that Kennewick Man (a human who lived in what is now Washington State, USA 8,358 ± 21 14C years before present) is European in ethnic origin. These people are obviously not informed of the genetic study done on The ancestry and affiliations of Kennewick Man which revealed him to be most closely related to modern Native Americans.
The genetic admixture which most closely relates Kennewick Man, Native Americans, and other East Eurasians with Europeans comes from the Ancient North Eurasians (ANE), a population living in Siberia at least 24,000 years ago which was most closely related to early West Eurasians (link, link). Ancient Y chromosomes of this ANE group, uncovered from Mal’ta (MA-1) and Afontova Gora (AG3), belong to the Y chromosomal haplogroup R, a branch of the Y chromosomal haplogroup P which diversified c. 31,900 years before present. Some migrations out of Siberia after this time are likely responsible for the current predominance of Y chromosomal haplogroups Q and R (branches of P) in Native Americans and Northern Europeans, respectively (I happen to belong to R-L513), as well as the ANE admixture found in these groups.
Davidski at Eurogenes also suggests (link) that there may have been a very early incursion of ANEs into the East Eurasian gene pool. If this is true, it may be responsible for the predominance of certain non-P lineages of Y-haplogroup K2, including K2a, K2b1, K2c, K2d, M, N, O, and S (which diverged from the ancestor of haplogroup P around 45400 years before present) among a variety of East Eurasians including the Ust’-Ishim Man from Siberia 45,000 years ago. Keeping in mind that the ANEs were most closely related to early West Eurasians, it is also possible that such an early incursion of ANE admixture is responsible for the East Eurasian presence of Y haplogroup C, which diversified ~47,900 YBP and was also found in some ancient West Eurasians such as Kostenki-14 and the Mesolithic La Brana specimen. Regarding the impact on mitochondrial (maternal) lineages, an early addition and ANE admixture to the East Asian gene pool may have brought mitochondrial haplogroup N which is normally found in West Eurasians, but is also significantly present in some very disparate East Eurasian populations such as Australian Aborigines, and certain Siberian and Native American peoples (and even the Ust’-Ishim specimen).
East Asians such as the Han, Koreans and Japanese also appear to have received a later addition of ANE admixture, but it was much less than that received around the same time by Siberians and the Siberian ancestors of Native Americans (see the supplementary data on pages 145-147 in here). Kennewick Man appears to have received 40-45 % of his genome from this later ANE admixture event; the Han, Koreans and Japanese received about 10-12 %, and the Andamanese Onge, an isolated population in the Indian Ocean, presumably received little to none and was used as a control in the analysis.
What East Eurasians (including Australoid peoples, East Asians, Native Americans, and Siberians) possess which differentiates them from West Eurasians (“Causaoids”) is admixture from another, apparently basal East Eurasian group which diverged 60,000-65,000 YBP from other Eurasians. This basal East Eurasian group seems a likely origin of the East Eurasian presence of Y haplogroup D (which is basal to all other Eurasian Y haplogroups except for E) and mitochondrial haplogroup M, which both formed between 60,000 and 65,000 YBP. Perhaps not coincidentally, both mitochondrial haplogroup M and Y chromosomal haplogroup D reach relative maxima in Tibet and Japan. Somewhat surprisingly, however, Y haplogroup D also diversified around the same time as Y haplogroups C and K2 (~45,000 YBP). This would seem to indicate that the East Eurasian gene pool underwent a population bottleneck until around 45,000 YBP when it received a large amount of ANE admixture (which appears already present in the Ust’-Ishim man from this time period). Under this model, over the next ~40,000 years, the East Eurasian gene pool underwent a massive geographic and genetic diversification.
I have decided to reevaluate my views on the application r/K selection theory to humans as done by Rushton and the Anonymous Conservative (whom I will refer to as AC). The blogger RaceRealist made a fairly good case that Rushton’s application (and by extension AC’s) of r/K selection theory to humans is based on false premises.
Race Realist responded to me in the following comment:
Thanks for being objective. That’s rare to find nowadays.I’ve spent years researching Rushton’s theory and thinking about how it applies to humans. Then I thought ‘Why only read what I agree with here when I don’t do that for other things?’ Then I found Judith Anderson’s ecology critique and then I went back to read the Graves paper that I just handwaved away.Rushton’s misapplication of r/K theory was based on Pianka’s (1970) r/K continuum. That’s wrong. Describing behaviors as ‘r’ or ‘K’ is stupid. r and K describe agents of selection. Endemic disease is an agent of K while cold winters are an agent of r—which Rushton completely reversed! He literally arbitrarily put r-selection to Africans and K to Eurasians because it ‘fit with the data’. True—it did.However where he went wrong was 1) treating human races as local populations (he’d need to look at one population in one ecosystem and compare it to another in a different one. These populations can be on the same continent (Africa) or two different ones (say, Africa and Northern Europe). 2) to apply the theory based on behaviors in modern environments makes no sense. Organisms MUST be studied in the environment that the selection was hypothesized to have occurred. Not doing so means it’s fine to disregard what he says about r/K selection in application to humans. Even omitting the racial comparisons doesn’t save it. 3) Evolutionary biologists and ecologists don’t even use the theory anymore.I’ve brought this up to PumpkinPerson and he won’t take to it. I’ve explained to him that Rushton reversed r and K for humans (if it were applicable to us) and he still spews Rushton’s garbage. I know that it’s tough to change your beliefs and then the backfire effect occurs (which occurs when you’re presented with new information then do anything you can to find information to back what you originally thought after presented with said new information). That’s one cognitive bias I’ve learned to nip in the bud recently. I’ve also found it much easier to change my view by reading new information myself.Now I’m at the bookstore every week in the biology section buying new books (I did this anyway) that are the opposite of what I believe to see what I think after. Constantly reevaluating your views is the logical—and intellectually honest—thing to do.So anyone who pushes this theory is pushing a wrong theory, and applying it to other aspects of our lives also makes no sense. Behaviors are not ‘r’ or ‘K’. Behaviors are responses to the selective agent—whether it is r or K. People like Anonymous Conservative, Stephan Molyneaux and the other guys you brought up then—by proxy—push a wrong theory. Read the papers provided and follow the references to read more in depth about how to apply it—and why it’s not in use anymore.This, then, leaves use with one troubling conclusion: anything based off of Rushton’s r/K selection theory is wrong by proxy. Rushton didn’t understand evolution and life history theory (r/K selection). I saw one critique of Rushton’s theory saying that ‘only a bad person would push a theory like this’. That’s a flawed retort. Ad hominem attacks in scholarly discussion do not work. Theories like Rushton’s must be deconstructed to show how and why they are wrong, lest other people believe something that is horribly flawed and incorrect.I’ll most definitely be showing others how and why Rushton is wrong as well. Rushton was wrong about a ton from penis size to testosterone. This is just the nail in the coffin.Rushton didn’t even reply to Graves or Anderson in print, take that for what you will.
… so now you know the gist of the problem I suppose.
Personally speaking, some of AC’s views have rubbed me the wrong way, largely because of his sometimes neoconservative bent. This is not to say he does not have more praiseworthy and transcendent ideas, he does, but this still does not overshadow larger problems: that r/K selection was not applied in the way it theoretically should have been, and that the theory itself is discredited: see RaceRealist’s recent blog post for details.
I previously wrote a post on Tolkien’s Elves and r/K selection theory, in which I described Tolkien’s elves as a K-selected ideal in a universal sense. I now reject this idea. However, as I mentioned in my earlier post, the elves have managed to follow an evolutionary strategy which gives them high fitness in their usual habitats. Thier phenotypes are also characteristically Northern European. So I still think of the elf as a biological ideal, but not in a universal sense of being “the measure of all things”. Rather the elves are a particular aristocratic ideal of the Germanic and to a certain degree Insular Celtic peoples who first conceived of them in their mythologies (and yes, just as some elves have dark hair, a minority of Germanic people such as King Halfdan the Black did/do as well).
From a Jungian perspective, the elf is an archetype which is part of the collective unconscious of Northwestern Europeans. It is, in my view, what would normally direct them (or perhaps I should say us given that I am a NW Euro) on a eugenic evolutionary path. This can be completed through selection for biological fitness in one’s environment and through endogamy within a biologically related clade or “subrace” (while excluding 1st – 3rd cousin marriages). The result is a eugenic biological transcendence from the parent race, and species, to form a new aristocratic clade.
As an end note, the current demographic pressures on the NW European gene pool may act as the refining fire from which a new aristocratic clade will emerge. Remember: it is always darkest before the dawn and what does not kill us will only make us stronger.
Interesting article on ethnocentrism:
Recently there has been a major comments war on Amerika.org regarding the website moderator’s take on one of my posts which I published a few weeks ago. Dare I import the war onto my own blog? Apparently, I am insane enough to do this.
Do the Irish have “negroid” admixture?
(The following map includes both Sub-Saharan and North African components)
Apparently not [the data for this map gives 0% African admixture to the Irish].
West Asian (Northern Middle Eastern) admixture?
It is found at low frequencies throughout Northwestern Europe.
Admixture related to Semitic peoples?
There is a small amount in all Europeans except for a few Eastern Europeans, the Saami, Finns, Basques, and Catalans.
Martian admixture? (someone actually suggested this!)
Give me a break.
So what makes the Irish a little bit different from the English, and pulled slightly in the same direction as Iberians are on a genetic principal component analysis?
A bit more Atlantic admixture (combination of Neolithic farmer and Mesolithic hunter-gatherer) most likely from the Megalithic period is responsible for this. The Irish have more than the English, but the English have some of this admixture as well. It peaks in the Basques, is relatively high in Eastern Iberia and the “Celtic Fringe”, followed by other geographically Western European populations, but is much lower in the Eastern Mediterranean, Near East, and Northern Africa.
This admixture peaks in the Basque population and appears to be a blend of Near Eastern Neolithic farmers and Mesolithic European Hunter-Gatherers. It matches mostly the extent of the Atlantic Megalithic culture. Several ancient samples were added to GEDMatch and analysed with Eurogenes K15. Nine Megalithic Iberian samples (3211-1518 BCE) had an average Atlantic percentage of 38.8%, similar to modern Basques. Three samples from the Remedello culture in Late Neolithic northern Italy (3483-1773 BCE) scored an average of 35.2%, considerably more than modern Italians, even Sardinians. One Megalithic Irish sample from Ballynahatty had 32.7% of Atlantic, about the same as modern Irish people. (source)
If you don’t like these admixture maps, then go argue with Maciamo Hay on Eupedia about them. I have my own life to live.
There has apparently been weak communication between the faction of the Right which considers r/K selection to be influential in politics and the faction (usually HBD folks like Evolutionistx and RaceRealist) who have either not expressed such views or rejected them.
Whichever side is correct, it seems apparent that patrifocal societies (Confucian, Indo-European, Abrahamic) are more right-wing/Authoritarian and more matrifocal ones (modern Sweden, many modern Germanic speaking countries) are more Left-wing/Totalitarian. Politics may ultimately depend on if women are trying to appease men (right-wing), or men trying to appease women (left-wing).
Still, r/K selection theory should be discussed so that the truth might be deduced on this matter.
Argue at will! (even if this is an old post by the time you come across it).
[if no one argues here, then argue somewhere else so that the reactosphere can reach a consensus on this issue]
There has been some dispute caused by uninformed persons on the dissident Right (
not naming any names Amerika .org) regarding the nature of Irish ancestry. I will attempt to clarify this as much as possible.
About two years ago, some British newspaper headlines written by people who seem to know very little about population genetics implied that the Irish are Middle Eastern (here, here). They are only correct in that all extant Europeans, Irish included, have significant admixture from early Neolithic Anatolian farmers. However, in order to correctly understand European genetics, one must do more than reading newspaper headlines. If the bozos who wrote them had actually read through the study they were basing their claims on, and understood its significance in the context of current population genetics, then they would realize that the Irish are essentially Northwestern Europeans (but that doesn’t make for a good eye-catching sensationalist story, now, does it).
The Irish genetically cluster and overlap to a significant degree with other Northwestern European samples, and appear most closely related to the British. They are not Southern Europeans, genetically speaking. Here are principal component analyses from two separate studies showing this. In the second analysis, the Irish are practically indistinguishable from the British and also overlap with Norwegians and Dutch.
Even if one wishes to do a fine-scale analysis to reveal the genetic difference between the English and the Irish, there is still obvious genetic overlap, and the English themselves have some Insular Celtic (Irish related) ancestry in addition to Anglo-Saxon ancestry.
The Irish and all Insular Celts appear to owe the vast majority of Y-chromosomes (haplogroup R-L21), as well as their autosomal ancestry to Bronze Age inhabitants of the British Isles c. 2000-1500 BC (link). The figure below shows the varying affinities of prehistoric Irish and Hungarian genomes towards modern European populations. (The fact that the Neolithic Irish sample resembles modern southern Europeans does not mean that the modern Irish are Southern European, rather all genetic samples from the Neolithic in Western and Central Europe prior to the Indo-European expansion resemble those of southern Europeans, particularly Sardinians; see the analysis at the bottom of the page).
The Bronze Age Irish, from whom modern Irish are descended, were autosomally very close to contemporaneous Indo-European peoples in Scandinavia (Nordic Bronze Age), and the continent (Unetice culture) (see analysis below). This is the reason why the Irish to this day are genetically Northwestern Europeans, just as the British, Germans and Scandinavians are. The cause of genetic variation between these groups is not that one group possesses a type of admixture that the others do not; it is because of small variations in the proportions of Neolithic farmer, hunter-gatherer, and Steppe related admixtures.
There are frequent disputes among some concerned with human biodiversity regarding the nature of the “white” racial type, given that there are multiple subraces which exist in Europe. There is a common approach (usually made for political convenience) to assume that the differences between these groups are insignificant. I would argue that this is generally a false assumption from an empirical standpoint, though all these groups are broadly classifiable as racially Caucasoid.
The Cro-Magnoid Type
The Cro-Magnoids (including the “Baltids” of Northeastern Europe) are likely one of the earliest Caucasoid phenotypes; they are often characterized in contrast to later Neolithic phenotypes by a robust skeletal build, a more brachycephalic cranium, and robust facial features. There tends to be variable skin and hair pigmentation, but eye color is usually light. This combination of physical traits is currently sometimes found in Balts, Northern Slavs, Estonians, Finns, Germans, the western Irish, Icelanders, and western Norwegians. It seems to have an antecedent in the Loschbour specimen from Luxembourg in the Mesolithic, c. 6000 BC which had robust features, and most likely light eyes, and dark hair and skin based on genomic testing (link). The populations in which modern Cro-Magnoids exist not surprisingly possess large quantities of the “WHG” (West European Hunter Gatherer) ancestry similar to that of the Mesolithic Loschbour specimen (shown below). It should be noted that throughout most of its present range, the Cro-Magnoid subracial type occurs alongside Nordics which emerged in the late Neolithic through Early Bronze Age. (Cro-Magnoid hunter-gatherers are also one population ancestral to Nordics). Oftentimes the Cro-Magnoids and Nordics are blended; this is common in most Germanic peoples.
The genetic research of Iosif Lazaridis (here, here) indicates that European Mediterraneans derive most of their genetic ancestry from a series of Near Eastern migrations into Europe, especially that of early Neolithic Anatolian cereal grain farmers. This early Neolithic ancestry may be the original source of the more dolichocephalic cranium, gracile build, and often neotenous facial features common to both Nordics and Mediterraneans. The lifestyle, social, and dietary changes of the Neolithic revolution may have been what selected for these new phenotypes in the first place. Most Mediterraneans living south of the Alps, Balkans and the Pyrenees, with the exception of Sardinians, also possess a significant genetic contribution from Bronze and Iron Age incursions from the Near East of the Phoenicians, Sea Peoples, Etruscans (possibly from Lydia), and possibly the Pelasgians (if they happened to be of Bronze-Age Near Eastern descent).
The first map below shows a rough approximation of total Near Eastern admixture in Europe, including both Anatolian Neolithic admixture and later Bronze and Iron Age incursions using data from this study. The second map shows only the admixture from the more recent Near Eastern incursions during the Bronze and Iron Ages:
The abundance of Near-Eastern ancestry in Mediterraneans compared to other Europeans is evident in the phenotypes of a slightly olive complexion, dark wavy hair, and dark eyes. Amphorae and busts from ancient Greece would seem to indicate that the majority of the population and some prominent aristocrats, particularly in Athens (such as Pericles), were of a predominantly Mediterranean phenotype, having dark wavy or curly hair which is much less common in Northern Europe.
The Mediterranean subrace, however, is not limited to Europe, or even the Mediterranean basin (this is indicated by the Lazaridis study on early farmers). Indo-Iranians of a Mediterranean racial type are largely descended from Iranian Neolithic farmers from the Zagros mountains. Arabs gain most of their Caucasoid ancestry from the pre-Neolithic Natufian culture of the Levant. The ancient Egyptians, whom we now know were Mediterranean Caucasoids, appear to derive their ancestry from both the Anatolian Neolithic and also the Natufian culture (given their genetic proximity to modern Levantines and Arabs) (link). All of the prehistoric cultures which gave rise to peoples of a Mediterranean subrace, do however share significant admixture containing a combination of European hunter-gatherer and “basal Eurasian” DNA. This “basal rich” admixture, as it is called on the blog Eurogenes, might be considered proto-Mediterranean; it most likely emerged in Northern Africa or the Middle East, though it is distinct from the Sub-Saharan African genetic admixture. While this basal rich admixture is most abundant in racially Mediterranean populations, it is, in fact, ubiquitous in all extant Caucasoid populations.
The Nordic subrace possesses a clear geographic range including the British Isles, Northern France, the Low Countries, Northern Germany, and the shores of the Baltic Sea, extending to some degree into Russia. The genetic research of Allentoft and Lazaridis indicates that Nordic populations possess most of their ancestry from three earlier Caucasoid groups: Anatolian cereal farmers, Pontic Steppe pastoralists (most likely Indo-European), and European hunter-gatherers, which began combining in the Northern European Corded Ware Culture in the Late Neolithic to Early Bronze Age c. 3000-2300 BC.
The very light skin pigmentation often found in Nordic populations was most likely a result of a need to effectively synthesize vitamin D using sunlight at high latitudes. The high degree of lactose tolerance, a neotenous trait found particularly in Western European Nordics is a result of the bovine pastoral economies of the Corded Ware and to a larger degree succeeding cultures which depended on milk as a dietary staple. The light pigmentation of the hair and eyes found in Nordic populations are also neotenous traits in Caucasoids. Nordics possess a gracile skeletal build and cranium bordering between mesocephalic and dolichocephalic tending towards facial neoteny (as with Mediterraneans, these skeletal features likely originate in Neolithic farmer ancestry). This unique combination of phenotypes in pigmentation, skeletal features, and elsewhere, makes the Nordic subrace distinct from other Caucasoids. It may have arisen partially through a sexual selection for generally neotenous traits.
Note how the distributions of the Nordic phenotypes below are similar to that of the Corded Ware Culture, where the Nordic subrace most likely began to emerge:
Culturally and genetically succeeding the Corded Ware people were those of the Nordic Bronze Age (Germanic), Atlantic Bronze Age (pre-Celtic?), Unetice culture (Italo-Celtic?), and Sintashta culture (Indo-Iranian, also where the earliest chariots appear). Genomes which have been collected from these cultures cluster together with each other on a genetic principal component analysis (here, here) and also cluster with modern Germanic, Celtic, and some Baltic and Northern Slavic ethnic groups (many Balto-Slavic peoples also have strong genetic influence from earlier hunter-gatherers, i.e. Cro-Magnoids). It is also apparent from these analyses, and even physical appearances, that modern Indo-Iranians, particularly in Afghanistan and Tajikistan, have some Nordic European ancestry in addition to their mostly Iranian Neolithic/Mediterranean ancestry. This is due to the Andronovo expansion of early Indo-Iranian speakers from Northeastern Europe into Central Asia c. 1500 BC. This expansion played an important role in the spread of Indo-European language culture into Central and Southern Asia.
Nordic phenotypes also occur sometimes in the Mediterranean and the Balkans. The Celtiberians, Myceneans, and early Italic tribes who introduced Indo-European languages into the Mediterranean from the north would have carried Nordic traits with them. Classical literature would seem to substantiate this. Many Greek mythological figures such as Menelaus, Achilles, Apollo, Aphrodite, and Athena are all described as having light pigmentation. Certain Roman patricians such as Augustus and Marcus Junius Brutus (the younger) possessed Nordic facial features. Augustus and many other Roman emperors also possessed, according to records, light pigmentation of the hair and eyes (link). Later, the Visigoths, Suebi, and Ostrogoths would add to the Nordic component in the Balkans, Italy, and Iberia. This would remain visible in the aristocracy of Spain for 1000 years after these invasions; Queen Isabella de Castille, born in 1451, possessed strikingly Nordic traits compared to the average Iberian, and even her own husband.
Brachycephaly (broad-headedness) is most exaggerated in Caucasoid populations inhabiting mountainous areas, hence the label “Alpine” is sometimes applied to this phenotype. When Neolithic mesocephalic and dolichocephalic populations interbred with Mesolithic hunter-gatherer populations, they may have acquired brachycephaly as an adaptation which proliferated in high altitudes (possibly to prevent high-altitude cerebral edema, but this is merely an educated guess). One example of this may be the brachycephalic people of the Neolithic Bell Beaker culture which became widespread in Central and Western Europe c. 2500 BC. This phenomenon of selection for brachycephaly in higher altitudes could be the reason why the round skull shape is still so commonly found in and around the more mountainous areas of Europe such as the Massif Central in France, the Alps, the Apennines, the Carpathians and the Balkans.
The “Alpine” phenotype is also present in the contemporary populations of the Caucasus region and the Armenian plateau, giving rise to a subrace sometimes referred to as “Armenoid”. These populations appear to be descended, based on genetic analysis, from the Neolithic and Paleolithic inhabitants of Anatolia and the Caucasus. In addition to this, given that the region encompassing the Armenian plateau and Anatolia is where animal domestication and bronze metallurgy began in the Neolithic, it is probable that many of the first animal herders and bronze smelters possessed an Alpine phenotype. These early herders and bronze smelters would have expanded the distribution of their Alpine phenotype as they migrated into Southeastern Europe and into Mesopotamia where the earliest civilizations arose.
This expansion out of Armenia and the Caucasus seems to be related to the distribution of Y-haplogroup J2 (edit: especially the J2b M102 subclade) and autosomal admixture from the hunter-gatherers of the Caucasus and Late Neolithic (Chalcolithic) Iranians. It may be responsible for the brachycephaly observed today specifically in Southeastern Europe, where there is little admixture from the European Mesolithic. This would be in contrast to France and Central Europe where there is more Mesolithic European ancestry, and that is the likely source of the brachycephalic (Alpine) phenotype.
It is probable that the brachycephalic Bell Beaker people of Central Europe (given that they possessed significant Anatolian Neolithic and Corded Ware-like ancestries) were the beginning of a heavy combination of Alpines with Nordics and Mediterraneans resulting in the “Dinaric” subrace. This Dinaric subrace most likely expanded to its present distribution first within the Bell-beaker culture itself, then by means of the Illyrians, Halstatt Celts and proto-Italic peoples who migrated out of Central Europe starting c. 1200 BC (It is also interesting to note that the Y-chromosomal haplogroup which is most associated with continental Celts and early Italic tribes, R-U152, was also found in a Bavarian Bell Beaker individual, RISE563). These expansions played an important role in spreading bronze, and later iron metallurgy throughout the European continent. The Slavic peoples of Central Europe may have also played a role in the expansion of the Dinaric subrace later beginning around 500 AD.
Conclusion: What is White?
Returning to the main dilemma which many are facing; one might like to ask the question of what is white? All commonly called “whites” are racially Caucasoid. In most formal discussions, “White” is often equated with Caucasoid, and can thus include both Middle Eastern and European ethnic groups. In more common or “folk” parlance, white usually refers to Caucasoids with a fair skin phenotype common in populations with an abundance of Nordic racial ancestry. It is difficult to simply equate the term “white” with pre-multicultural European descent because of the multitude of Caucasoid subraces already present in Europe prior to recent multiculturalism, some of which extend outside Europe into the Middle East. Hence, when speaking accurately with regards to genetic ancestry, “White” should either refer to “Caucasoid” or to racially Nordic Caucasoids. If the former option is chosen, Europeans may be considered “white-Europeans” or “European whites”. What all extant Europeans share is significant ancestry from Anatolian Neolithic farmers, and this gives rise to a certain degree of pan-European clustering on genetic principal component analyses.
Without getting into details, there are a variety of European ethnic groups in the US today belonging to different European subraces. The best way for ethnic nationalists to sort this out from a natural law standpoint is to use free association to allow various European American ethnic groups to coalesce in certain territories as they desire and to gain power regionally and thus avoid ethnic conflict.
Addendum: Non-Caucasoid Admixture in Majority Caucasoids
To address this topic I will use the Eurogenes K7 admixture calculator which uses Caucasoid admixtures sourced from ancient populations prior to the Neolithic, Bronze age, Iron age, and Medieval population movements. When viewing the spreadsheet, the populations ancestral to all modern Caucasoids are labeled “Villabruna-related”, “Ancient_North_Eurasia” and “Basal-rich”. East Asian ancestry is called “East Eurasian”, and Sub-Saharan African ancestry is referred to as “Sub-Saharan”; the “Southeast Asian” and “Oceanian” ancestry groups are predominate in Australoid populations.
Modern Semitic populations in Arabia and the Levant have little to no Australoid admixture and trace Sub-Saharan African admixture at around 1-3 % as well as some occasional East Asian admixture at ~0.5%. The Druze, Samaritans, and Lebanese Christians lack this additional East Asian and Sub-Saharan African Admixture. Most modern Indic and Iranic populations, except for some Kurds and Zoroastrian Iranians, possess some East Asian admixture (~1-9%), and Australoid admixture (~0.4-9%). Middle Eastern Islamic populations almost as a rule possess more non-Caucasoid admixture than Middle Eastern populations which have remained non-Muslim. This may be due to the conversion of Central Asian Turkic peoples and Sub-Saharan Africans to Islam. Ironically, some modern linguistic Turks, living in Trabzon, possess no more Sub-Saharan African, or East Asian ancestry compared to most Europeans.
Europeans, in general, do not possess much Sub-Saharan African ancestry, almost invariably under 0.2% in most of Europe (usually fluctuating greatly below this level in the same populations; an indication of calculator “noise”). In Europe, Sub-Saharan African admixture reaches maxima of 0.2-0.5 % in Sicily, and 0.5-1% in Portugal. 96 % of European Americans possess less than 1% Sub-Saharan African Admixture according to 23 & Me (link). East Asian admixtures are present at .5-2% in West Russian, Ukrainian, and Eastern Baltic Populations. Russians in Kargopol are ~4-6 % East Asian. Finns have roughly 6-7% East Asian admixture; the Saami possess about 20% East Asian admixture. Other European populations have between 0.01 to 0.5 % East Asian admixture, often possessing almost this entire percentage range within the same populations, possibly indicating calculator noise at this level. Australoid ancestry fluctuates erratically in the European continent between 0.0 % and 0.8 %, possibly a sign calculator noise, or of certain populations possessing minimally less genetic drift away from the ancestral Eurasian population dwelling in India 70,000 years ago.
Generally, below a certain level, trace genetic admixtures are able to be considered “noise” or erroneous defects caused by the imperfection of the genetic model used to calculate admixture percentages. However, it seems likely that millennia of proximity with neighboring Uralic populations has led to the small peak in East Asian admixture among the Eastern Slavs and Balts, and that admixture from invading Moors gave a very small amount of Sub-Saharan African admixture to Portugal and Sicily which is not present elsewhere in Europe. In time, these trace admixtures may be selected out of the populations which possess them just as Neanderthal ancestry in humans has decreased from 3-6% 40,000 years ago to 2% in the present day (study).