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Guide to Patagonia's Monsters & Mysterious beings

I have written a book on this intriguing subject which has just been published.
In this blog I will post excerpts and other interesting texts on this fascinating subject.

Austin Whittall


Showing posts with label native american. Show all posts
Showing posts with label native american. Show all posts

Friday, January 23, 2026

On the diversity of Native American genes


Native Americans are described as the least diverse human beings in the world, bottlenecks along the way depleted variation in their genetic stock, and the small founding population that reached America carried a tiny part of the originally diverse set of genes that they started out with.


However, it seems that there were different waves that reached America, and each one carried diversity, the Amerindians had plenty of varibility but this vanished when the Europeans reached America in 1492.


Eduardo Tarazona-Santos, Denise R. Carvalho-Silva, et al., (2001) in Genetic Differentiation in South Amerindians Is Related to Environmental and Cultural Diversity: Evidence from the Y Chromosome. AJHG, Vol 68:6, June 2001, Pages 1485-1496, https://doi.org/10.1086/320601, argues that it did not cause much difference, that diversity was lost in the distant past, not during European discovery and conquest:


They admit that the population reduction was more severe in Eastern South America than in the Andean region, yet argue that the reduced diversity was not caused by contact with Europeans, instead they suggest that "it has been shown that reduction of gene diversity (i.e., in average expected heterozygosity) began several generations later (Maruyama and Fuerst 1985; Cornuet and Luikart 1996). Therefore, the recent demographic depletion undergone by Amerindian populations 20–25 generations ago could not account for the differences in gene diversity evidenced in the present study, which are more likely to be related to more-ancient (i.e., pre-Columbian) demographic events."


Quilmes Indians exile

I disagree. The current distribution of natives was also impacted by the European conquest, populations were displaced in the Andean region, from rural areas to cities, from farms to mines, from their homeland to "reducciones" (Spanish word for subduing by force and concentrating in one spot, for easier control an domination), some were over 1,600 km (1,000 mi) from the natives' original homeland, like the Quilmes people, who walked from the Andean foothills in Tucumán to what is now a suburb of Buenos Aires, named after them, Quilmes. See the image (the map is from my website -in Spanish- on Argentina's Ruta 40 highway).

Even the Incas moved people from one part of their empire to another, to settle the newly dominated regions (Mapuches in Chile received an influx of Andean settlers, also the Chachapoyas.) This altered the original genetic patterns and still distorts modern samplings.


Further proof on the drastic decline of Native American populations can be found in Arnaiz-Villena et al., (2025): "After Columbus’s arrival in 1492 AD, the Amerindian population from Alaska to South America (about 80 million) was drastically reduced by 1552 AD (8 million) because of new European-borne diseases (mainly influenza, smallpox, and measles) and war. This drastic population reduction likely caused a genetic bottleneck, which explains why modern Amerindian HLA profiles do not always follow strict geographic patterns. The loss of genetic diversity may be attributed to the selective survival of certain alleles in populations able to present peptides derived from newly introduced pathogens."


The interesting note is the natural selection effect, as the natives died out but some adapted to the new environment, and this promoted the selection of certain genes, resistant to the new diseases, starvation, and exertion of forced work for the conquerors. The real survival of the fittest. 72 million people out of 80 million died, 90% of them! A gigantic loss of genetic diversity.


A similar argument is put forward by Michael H. Crawford (1998) in his work "The Origins of Native Americans: Evidence from Anthropological Genetics" (Cambridge: Cambridge University Press, 49–51, 260–261), quoted below:


"The Conquest and its sequelae squeezed the entire Amerindian population through a genetic bottleneck. The reduction of Amerindian gene pools to from 1/3 to 1/25 of their previous sizes implies a considerable loss of genetic variabilty in New World populations. Who survived the epidemics? It is highly unlikely that survivorship was genetically random."


He then makes the point that those who survived didn't do so by chance, but by natural selection of fitter traits:


"If Amerindians of today are different from their pre-Conquest ancestors with respect to many genetic systems, most likely those genetic traits that confered some selective advantage under the conditions of the Conquest are more numerous among contemporary Amerindians. Thus, the present gene-frequency distributions of Amerindian populations may be distorted by a combination of effects stemming from genetic bottlenecks and natural selection."


An additional factor mentioned by Crawford is the inflow of African slaves and Europeans: "In addition, the gene frequencies of the native populations were further modified by the massive gene flow or admixture with Europeans and Africans, thus possibly obscuring the pre-Conquest patterns. As a result, great care should be exercised in the interpretation of sophisticated multivariate analyses of gene-frequency distributions among New World populations based upon samples collected by various researchers utilizing a diversity of sampling techniques."


Crawford then asks why were Amerindians more susceptible to the diseases brought by the Europeans. In fact, these diseases were also lethal in the Old World, and the African ones, like Yellow fever also wiped out Europans, just as it killed the Native Americans.


He suggestst that "...the death toll from measles was no different than what was observed in European populations that had not been repeatedly exposed to the same disease.... In Europe, epidemics caused by smallpox, yellow fever, and influenza were extremely severe with high mortality. The mortality was somewhat higher in the New World because the disease effects were further exacerbated by starvation, slavery and physical exhaustion. Thus, it has been argued that Amerindians did not have any special sensitivity or susceptibility to imported Old World diseases." This is a novel idea for me, as I had imagined that in Europe and Asia, perhaps those equipped with a fine-tuned immune system, inherited from those who survived epidemics, and through epigenetic changes, created a population that was less susceptible to these diseases. It seems that the situation is different.


So, nowadays, when we look at the genes of "Native Americans" we are looking at what was left of the original diversity, distorted by natural selection over the 433 years elapsed since European discovery, and also, certain admixture of European, African, and also, Asian genes.


A study (Jorge Lindo et al., (2018). Patterns of Genetic Coding Variation in a Native American Population before and after European Contact. The American Journal of Human Genetics, Vol 102:5, 3 May 2018, pp 806-815. https://doi.org/10.1016/j.ajhg.2018.03.008) took a look at current Amerindian genes and the ancestral genetics (from samples taken from pre-contact skeletal remains) belonging to a group of natives, the Coast Tsimshian people living in Prince Rupert Harbour, British Columbia, Canada.


These people have lived there at least for the past 6,000 years and suffered a drastic drop in population after contact with the Europeans which in this part of America was later than in others. In the 1800s they were struck by smallpox epidemics and roughly 175 years ago their population declined by 57%. Then they admixed with people who were not Tsimshian, mainly natives of other groups, and Europeans.


The authors noted that diversity (genetic variation) is the outcome of mutation, recombination, migration, genetic drift, and natural selection, all of these factors played a role among these people.


They found that the ancient natives, compared to the modern ones, had "higher levels of mean observed heterozygosity within coding regions (mean heterozygosity across modern 1.230 × 10−4 versus ancient 4.935 × 10−4 individuals)." This is a fourfold difference.


Unexpectedly, the authors expected genetic drift to increase the frequency of certain alleles. The genetic drift would be a consequence of the collapse and slow recovery. However, they found that this didn't happen. They attributed this to the "relatively short evolutionary timescale within which these events occurred; and, second, the recent admixture with both indigenous and non-indigenous populations, which may have increased genetic diversity and countered the deleterious effects of reduced population size"


Another study by O'Fallon BD and Fehren-Schmitz L., (2011) (Native Americans experienced a strong population bottleneck coincident with European contact. Proc Natl Acad Sci USA. 2011 Dec 20;108(51):20444-8. doi: 10.1073/pnas.1112563108. Epub 2011 Dec 5. PMID: 22143784; PMCID: PMC3251087) looked into the effects of European contact: "We find that indigenous Americans experienced a significant contraction in population size some 500 years before the present (ypb), during which female effective size was reduced by ∼50%, thus suggesting that the impact of European colonization was both widespread and severe... the scale of the contraction suggests that the depopulation was not localized to particular regions or communities, and instead, was likely to have been widespread or to have had an especially severe impact on the most populous regions."


Comments

For all of these reasons I am always skeptical on genetic conclusions that are based on admixed, heavily diluted, Native American genes such as those using data coming from CLM: Colombians from Medellín, Colombia, PUR: Puerto Ricans from Puerto Rico PEL: Peruvians from Lima, Peru, or MXL: Mexican Ancestry from Los Angeles, California.


And when a paper uses DNA collected from an Amazonian tribe, the data is usually considered inadequate due to genetic drift and founder effects!


Sampling of ancient, and therefore "pure" Native American genes could provide a real, clear view of the rich diversity lost after 1492.



Patagonian Monsters - Cryptozoology, Myths & legends in Patagonia Copyright 2009-2026 ny Austin Whittall © 

Friday, October 31, 2025

Halloween & Patagonians


Halloween wasn't celebrated in Argentina on most of Latin America until recently. The typical Catholic festivity was All Saints' Day on November 1st, and until the late 1970s it was a National Holiday in Argentina. Mexico is known for celebrating the Dia de los Muertos to remember their dead relatives (Nov. 1 and 2).


Halloween is a recent cultural addition introduced by the TV, and American movies. We learned about trick or treat by watching them.


Patagonian natives had different beliefs about the dead, the Aonikenk believed that the dead person rode on his horses into the afterlife (see p. 308 - Source), so the relatives killed the horses of the deceased and placed them by the tomb. Among the Mapuche, there were propiciatory rituals that helped the spirit or püllü of the dead move on, from the material plane into the plane of their ancestors (Source).

There was also the belief among the Tehuelches that the dead went to heaven and lived in an enclosure of stars (the enclosure -like a pen- of the dead), where they enjoyed a good afterlife.


Subtitulo


An AI image I created on Halloween and Paleoindians & megafauna (weirdly inhuman).


Patagonian Monsters - Cryptozoology, Myths & legends in Patagonia Copyright 2009-2025 by Austin Whittall © 

Sunday, September 7, 2025

D4h3a mtDNA revisited


Yu-Chun, lI et al. published a paper in 2023, that looked into the link between Native Americans (NAs) mitochondrial DNA (mtDNA) lineage D4h3a and the variant D4h3b which until now has been found only in East China and Thailand.


The authors noted that "D4h3 and its ancestor type D4h are relatively rare in contemporary populations (∼0.5%)" and estimated the age of the NA variant at 19,400 years (15.11 - 24.05 ky).


The interesting part is that they suggest that this haplogroup took a coastal route by sea from China to America, going through Japan's Islands. It didn't cross from Siberia and Beringia into America, walking.


"The coastal distributions of the NA (D4h3a) and Japanese lineages (D4h1a and D4h2), in combination with the Paleolithic archaeological similarities among Northern China, the Americas, and Japan, lend support to the coastal dispersal scenario of early NAs."


The authors highlight that this is a genetic source that is outside of Siberia, which provided mtDNA (a matrilineal lineage) to Native Americans. They stress that it is an "additional ancestral source for the ancestors of NAs beyond Siberia", and that "although only contributed to a small proportion of the mtDNA gene pool of NAs (D4h3a) [it] would be important in complementing the whole picture of origination histories of early NAs."


Below is an image from this paper:


Given the location of the original D4h variant, on the coast of Northern China, the authors suggest that it could have dispersed along the Pacific coastal rim: "we speculate that D4h would have documented LGM and post-LGM dispersals along the eastern Pacific coast. This echoes well with the dispersal D4h3a along the Pacific coastal path when the ice-free corridor was closed. Similarly, Y chromosome C-L1373, which probably radiated in parallel with mtDNA D4h, has also been reported in South Koreans (http://koreangenome.org/) and the Nivkh, thus lending support to a coastal population expansion scenario initiated from northern coastal China. This, together with the Paleolithic cultural affinities along the Pacific, e.g., stemmed points, and the palaeoecological feasibility of maritime dispersals (e.g., kelp highway hypothesis) lends further support to the coastal route hypothesis of early NAs."


It is also found along the coastal people in South America. Stuart J. Fiedel (source) in 2017 wrote that "D4h3a is a relatively rare clade of haplogroup D... it was reported mainly from coastal peoples, including the Fuegians of southernmost Chile, the Chumash of southern California, and the Cayapa of Ecuador The 10,300-year–old skeletal remains from On Your Knees Cave in coastal Alaska belonged to a derived clade of D4h3a."


However, Fiedel says that "the recent distribution of this clade is “deceptive” and has nothing to do with a hypothetical coastal migration".


He bases this argument on the fact that the Anzick baby had D4h3a mt DNA, and is roughly 12,900 years old, but it was found in south-central Montana, far from the Pacific coast, and that other remains are also from the interior of the continent like the Hopewell remains found in the Klunk Mounds in Illinois, and that this variant has been found in extant people of Native American origin in Peru, Bolivia, Brazil, and Mexico.


I had posted about D4h3a back in 2014 and pointed out the same idea:


"We see that the D4h3a tends to have a coastal distribution along the Pacific Ocean from Canada to Tierra del Fuego: Canada, California, Ecuador, Southern Chile and Argentina.
The Yaghan, Alakaluf, Chono, Cayapa, Chumash and the man from On Your Knees Cave, all had this haplogroup.
They all built sea-going craft: rafts, dugout canoes, bark canoes and "sewn plank" canoes.
Other groups also built canoes or rafts; the Changos in Northern Chile, the Pericú, and the Aleuts, though we cannot tell if they also carried this rare haplogroup.
But, as we will see in our next post, it is also found quite far from the Western Coast: as it was detected in ancient remains from the Klunk Mound (Illinois) and in Shandong, China.
Furthermore, the Ainu people of Japan also built "lashed-canoes" -like the Chono and the Chumash (as well as dugouts), and they may have a link with the Amerindians.
"


It pointed out the Chinese connection, the coastal route, and the original Japanese people, the Ainus. The second post in that 2014 series reported the Klunk Mound remains with this haplogroup variant and proposed that "This haplogroup was widespread across America (Pacific coast and well across the Rockies) and became extinct among all native groups being replaced by the other more common haplogroups now found in those groups (A, B, C, D). These surely migrated later into America." It also suggested a back-migration from America to Asia.


Let's see what future investigations find.


My nest post will be about the Cayapa people of Ecuador.



Patagonian Monsters - Cryptozoology, Myths & legends in Patagonia Copyright 2009-2025 by Austin Whittall © 

Tuesday, December 17, 2019

Horn Rock Shelter a skull 11,000 years old with a distinct morphology


Horn Rock Shelter is located in Texas, and is the site of a double burial, a middle aged man (37 - 44 years old) and a girl of 10 - 11. Apparently the man was a shaman. Girl and shaman were buried together in this cave as shown in the image below (girl on the Left).


A recent comment on my Chapala "homo erectus" brow ridge revisited post prompted me to look into this site and its oddly shaped male skull (Thank you William).


You can read about the site, the skeletons and the tools and articles found in the grave, in this article: New Look at the Double Burial from Horn Shelter No. 2, by Margaret A. Jodry and Douglas W. Owsley 2014.



The remarkable point seems to be the shape of the man's skull, as portrayed in National Geographic, from which this image (below) was taken:



The skull appears to have distinctive features yet this paper says that there were "no significant differences" between the Horn individuals and later Central Texas populations.


This is a reconstruction of the male skull:


Notice the brow ridges. Credits

The bust depicting how the shaman looked when he was alive also displays prominent brow ridges:



The remains are old, 11,100 years BP, and surely reflect the great morphological diversity of the Paleoindians, lost during the depopulation of the Americas due to illness brought by the Europeans after 1492 (flu, measles, small pox, just to mention a few), diseases which wiped out millions of Native Americans in a few years.


There are several news articles dating to the period 2010-15 that mention samples having been taken for DNA analysis, but no results have appeared in print as a formal paper, only articles in newspapers. But they are interesting:


Waco Tribune Herald, 2010: "The handful of other ancient American remains whose mtDNA has been studied carry one of the five genetic markers that various Native American groups share. Not so with the Horn Shelter bones, according to numerous tests Baker has done so far.
'The results are different from what you'd expect from Native Americans,' she said. 'I'm looking at the sequence and I'm not able to determine a haplogroup. . . . Usually, when I run the sequence, I get something very clear.'
Baker is planning to send the bone samples to another laboratory for retesting to see if her results can be replicated"

KWTX, 2017: "Dr. Doug Owsley, head of the division of physical anthropology at the Smithsonian, said DNA material has been successfully recovered from the bones of a little girl recovered at the Horn Shelter, but analysis has not yet been completed.
He also said scientists failed in their effort to recover DNA material from adult bones found in the same grave, but are now trying a different technique to recover the material.
"


The local Museum at the site (Bosque Museum) published in 2013: "Dr. Lori Baker of Baylor University has received the most recent DNA results on the Horn Shelter Man. We are awaiting the publication of her report to find out what the results show. Earlier DNA studies showed that Horn Shelter Man was not related to modern Native Americans."


There is a paper: 2012 Pack, FL, Hulsey, BI, and Cabana GS. "Report on DNA Findings for the Horn Shelter Site." Report submitted to Dr. Lori Baker, Baylor University.

It is surprising that the results have not been revealed after all these years...



Patagonian Monsters - Cryptozoology, Myths & legends in Patagonia Copyright 2009-2020 by Austin Whittall © 

Saturday, July 13, 2019

Siberians are not that close to Native Americans


Siberians are said to be the direct ancestors of Native Americans. These Siberians moved into the Beringian land bridge and from there crossed into North America and spread across the whole continent, peopling the Americas, or at least that is what the story says. But what are the facts?


A recent paper: The population history of northeastern Siberia since the Pleistocene, by Martin Sikora et al., Nature vol 570, pp. 182 June 13, 2019, https://doi.org/10.1038/s41586-019-1279-z, describes their findings after sequencing the genomes obtained from 34 ancient remains across Siberia. These genomes span ages ranging from 600 to 31,600 years ago.


These genomes also include the northernmost pleistocene remains found in Siberia, at Yana RHS: they are the earliest direct evidence of human presence in northeastern Siberia, a population that they refer to as Ancient North Siberians (ANS).


Their conclusions are interesting: (bold is mine)


"We find that—despite the complex pattern of population admixture throughout the past 40,000 years the first inhabitants of northeastern Siberia (represented by the Yana RHS individuals) were not the direct ancestors of either Native Americans or present-day Siberians, although traces of their genetic legacy can be observed in ancient and modern genomes across America and northern Eurasia.
These earliest ancient Siberians (the ANS) are known from a handful of other ancient genomes (those of the Mal’ta and Afontova Gora individuals); they are the descendants of one of the early modern human populations that diversified as Eurasia was first settled by our species, and are thus highly distinct.
The ANS were later partially assimilated with a group with East Asian affinity who formed the Ancient Palaeo-Siberians (represented by Kolyma1); this group also probably once had a wide geographical distribution across northern Eurasia. The genetic legacy of Ancient Palaeo-Siberians among present-day Siberians is more limited, being restricted to groups in northeastern Siberia.
"


They found that "Despite their extreme northeastern Siberian geographical location, the Yana RHS individuals are genetically closer to West Eurasians".


They have to look to a later date to find a Siberian that is closer to Native Americans: "We find that the Kolyma1 individual (dated to 9.8 ka) who represents a lineage that formed after about 30 ka, which we name ‘Ancient Palaeo-Siberian’ documents the first major genetic shift that we observe in the region ... Principal component analysis, outgroup-f3 statistics and mitochondrial DNA and Y chromosome haplogroups (G1b and Q1a1b, respectively) demonstrate a close affinity between Ancient Palaeo-Siberians and present-day Koryaks, Itelmen and Chukchis, as well as with Native Americans."


But Kolyma1 remains, found in northeastern Siberia, close to Beringia, are less than 10 ky old! So she cannot be an ancestor of the older American population which is now believed to have reached America at least 16 kya. Could Kolyma1 be the outcome of a backflow into Siberia, from America? Only about 66% of her genes is similar to that of Native Americans.


So Kolyma1 is the closest they could find to American Natives, however she isn’t an ancestor. Most of her genome belongs to the "Ancient Paleo-Siberian" lineage which split from that of the Native Americans some 24,000 years ago.

Interestingly, they report that "A signal of Australasian ancestry that has been observed at a very low frequency in some modern and ancient South American populations is not evident in any of the ancient Siberian or Beringian samples sequenced here, or in previous studies".


The study concludes that "the majority of Native American genetic ancestry is likely to have originated in northeastern Siberia rather than south-central Siberia, as has been inferred from modern mitochondrial and Y chromosome DNA."


To sum it up, the northernmost of the early Siberians (Yana) are not related to the people who supposedly peopled America. The later Kolyma woman is similar to but not an ancestor either, she is actually a later arrival in the area, when she died, America was already inhabited!


There is a paucity of remains between Yana and Kolyma1 which means that we have to wait for more remains to be discovered and studied before this issue is settled for good.



Patagonian Monsters - Cryptozoology, Myths & legends in Patagonia Copyright 2009-2019 by Austin Whittall © 

Saturday, December 15, 2018

The "unsampled population" in America: archaic hominins?


I want to share an excellent article from "Ancient DNA Era", published on Nov. 27, 2018 by Alberto (Early human dispersals within the Americas – Moreno-Mayar et al. 2018).


In this article Alberto discusses a recent paper (Early human dispersals within the Americas, J. Victor Moreno-Mayar, Lasse Vinner, Peter de Barros Damgaard, Constanza de la Fuente et al, Science 08 Nov 2018 DOI: 10.1126/science.aav2621) which deals with "multiple independent, geographically uneven migrations, including one that provides clues of a Late Pleistocene Australasian genetic signal, and a later Mesoamerican-related expansion. These led to complex and dynamic population histories from North to South America."


Moreno-Mayar mentions:


"We sequenced 15 ancient human genomes spanning Alaska to Patagonia; six are ≥10,000 years old (up to ~18× coverage). All are most closely related to Native Americans (NA), including an Ancient Beringian individual, and two morphologically distinct "Paleoamericans." We find evidence of rapid dispersal and early diversification, including previously unknown groups, as people moved south. This resulted in multiple independent, geographically uneven migrations, including one that provides clues of a Late Pleistocene Australasian genetic signal, and a later Mesoamerican-related expansion."


Alberto focuses on the "previously unknown groups" and the "Australasian genetic signal" and he quotes the original paper:


"...further SFS-based modeling indicates that Mixe most likely carry gene flow from an unsampled outgroup […] Hereafter we refer to that outgroup as 'Unsampled population A' (UPopA), which is neither AB, NNA or SNA [Ancient Beringians, Northern Native Americans or Southern Native Americans], and which we infer split off from Native Americans ~24.7 ka, ranging from 30-22 ka (95% CI; this large range is a result of the analytical challenge of estimating divergence and admixture times in the absence of UPopA genome data).[…] Under a model with a pulse-like gene flow, we inferred a probability of ~11% gene flow from UPopA into Mixe ~8.7 ka (95% CI: 0.4-13.9 ka; the wide interval potentially reflects unmodeled continuous migration)"


Alberto then reasons as follows: (I quote him extensively below)


" When they say "unsampled", they mean unsampled. So no, we’re not talking about potentially "anyone", but quite specifically about a population that does not only seem to be an outgroup to NA, but also an outgroup to Eurasians.
If this is true, then who can be an outgroup to Eurasians? Basically there are 4 options:
– An African population (meaning a population that went Out of Africa after the main OoA event that gave birth to most Eurasians, and that somehow reached Central America some 9 kya). This one is the least likely, really.
– An early OoA population (meaning a population that went OoA before the main OoA event). We know from archaeology (and with some support from genetics) that such early events did occur but they hardly contributed to later Eurasian populations (maybe a tiny bit to some SE Asian/Australasian populations?). So this one would mean that such population made it to the Americas and survived somewhere around Central America until the second major wave arrived.
– Archaic hominins. Like Neandertals or Denisovans. A small admixture from such groups (on top of what other NA already have) would make the shared drift of Mixe with all other AMH be lower. So is it possible that some form of archaic hominin lived in America and survived until some 9 kya?
– A fourth option would be an early "generic" Eurasian population, something similar to Ust-Ishim samples from 45 kya, but not directly related to Ust-Ishim.
"


I favor option three "Archaic hominins" but Alberto believes option four is the most likely one.


Finally Alberto remarks: "Using qpGraph, this Australasian admixture is estimated to be around 3% in these samples (and modern Surui). How it got there (if it’s real, that it well could be) is unknown at this point, but it’s important to keep in mind that it was already present at least 10.4 kya, so it cannot be from any kind of Holocene migration of Australasians to South America. The possibility is that there was a small (?) population of Australasian origin at the arrival of the migrants of NE Siberian origin."


Skoglund already noticed the Australasian link in Native American DNA (See paper here and the other paper here) back in 2015.


In my book Monsters of Patagonia y point out the similarity between Australian and Patagonian native myths (read more), and conclude " Human remains discovered in Brazil show a very strong resemblance to modern South Pacific people, suggesting that America was first colonized by the generalized human (Homo sapiens) population that inhabited East Asia in the Late Pleistocene. These people arrived in America in very ancient times long before the Mongolid morphology of the forbearers of the Clovis had evolved."


We will have to wait for more evidence to learn about the unsampled population and the Australasian migrants.


Patagonian Monsters - Cryptozoology, Myths & legends in Patagonia Copyright 2009-2018 by Austin Whittall © 

Sunday, October 18, 2015

Language diversity and the peopling of America


For years I have wondered why do Native American people speak so many languages? They supposedly reached the New World recently (i.e. 15,000 years ago) yet evolved over 40% of the global languages! A figure higher than that found in Africa, the "cradle of Mankind".


Africans have had the time (they are supposedly the oldest humans) and the advantage of not going through bottlenecks (I do imagine that bottleneck that wipes out genetic diversity does the same to languages... kill the speakers and the language dies), so they should have evolved most languages than any other group of humans. But they have not.


The diversity of Languages: highest in America. From [1]

Then we have the island of divesity in New Guinea has the highest language diversity in the whole world! 820 languages out of a global total of around 7,000. That is 1 language every 820 Papuans.


I found that quite reasonable, the island is a jungle, with many mountain ranges that isolate populations and keep them from mixinng. New Guinea has been considered as one of the first places reached by mankind during our epic trek out of Africa.


But America is different, we are newcomers. The Papuans had 50 ky to develop their languages, the Amerindians less than 15 ky. So how do we explain this?


To make matters worse, America's native population fell to half or even less during the period of discovery and conquest. How many languages were wiped out before even being discovered? Even so, it has the highest global language diversity.


The origin of languages


Human beings speak, and we are all aware that Chinese and English sound different, that Spanish, Italian and French may seem similar but are also different. We are humans and speak different languages despite having a common origin.


An early attempt to explain this can be found in the Bible (Genesis 11: 1- 9): "... But the Lord came down to see the city and the tower the people were building. 6 The Lord said, 'If as one people speaking the same language they have begun to do this, then nothing they plan to do will be impossible for them. 7 Come, let us go down and confuse their language so they will not understand each other.'" So God made us all speak different languages by an act of his almighty power. Neat and simple.


But we now know that humans originated longe before any ziggurats were built in Mesopotamia. Language is something that arose tens of thousands of years ago. According to Chomsky, Tattersall, Bolhuis and Berwick (2014), "The faculty of language is likely to have emerged quite recently in evolutionary terms, some 70,000–100,000 years ago" [3]. Of course (I have posted on this before) that date range is not inferred from language studies, it is taken from the date suggested by anthropologists as the date of emergence of Modern Homo sapiens. So if that date was not correct, then the date given for the origin of languages is also incorrect.


In fact, our next of kin, the Neanderthals, could and did speak: "From the consilience of evidence from anatomy, archeology, and DNA, one can conclude that some language abilities, if not necessarily full modern syntactic language, were present in Neanderthals" so perhaps the ability to speak in Neanderthals predates that in humans. [4]


Daniel Nettle [2] suggests that people living near the Equator live easier lives regarding food supply and can split into smaller groups, which favours creation of new languages: "Where the climate allows continuous food production throughout the year, small groups of people can be reliably self-sufficient and so populations fragment into many small languages. Where the variability of the climate is greater, the size of social network necessary for reliable subsistence is larger, and so languages tend to be more widespread."


And this makes sense, as you can see in the map below, language diversity is highest close to the warm equatorial areas:


The diversity of Languages: location of highest densities. A. Whittall

Interesting, but this explains the evolution of languages during the last 11,000 years after the discovery of agriculture. I cannot imagine a large society of hunter-gatherers all speaking the same language, but one of farmers and tax collectors does make more sense.


But how fast do languages evolve? Take Australian English and English English or American English. They Aussies and Americans split from the mother tongue between 250 and 400 years ago, and did keep in touch with the distant British Metropolis yet evolved distinct stress and intonation for the same words. Something similar has happened with Spanish in the different Latin American countries and Spain over the past 500 years. But change has been small perhaps due to the lack of isolation.



The image above, from L. Luca Cavalli-Sforza & Marcus W. Feldman clearly shows that American languages are different to those in Asia, the "source" of the Native Americans' ancestors. This is surely conveniently explained by the "Beringian standstill" (how convenient) which allowed the future Amerindians to differentiate from those remaining behind in Asia.


Last but not least, I usually read that all indicators of genetic diversity fall as you move away from Africa, a clear indication of an African origin for all human beings. But, this is not seen in the case of human language diversity. Why?


I do believe that we should look into language diversity as an indicator of an older origin for mankind as a whole and for an earlier date for the peopling of America.


For those interesting in reading about this subject in depth, German Dziebel has written about linguistic diversity in support of his Out of America theory. Read More, and see an analysis of it here.


Sources


[1] Mobility and Ancient Society in Asia and the Americas, pp 117-126, chapter " How America Was Colonized: Linguistic Evidence. Johanna Nichols
[2] Explaining Global Patterns of Language Diversity, Daniel Nettle, journal of anthropological archaeology 17, 354–374 (1998) article no. AA98032
[3] Bolhuis JJ, Tattersall I, Chomsky N, Berwick RC (2014) >How Could Language Have Evolved? PLoS Biol 12(8): e1001934. doi:10.1371/journal.pbio.1001934
[4] Language Abilities in Neanderthals By:Johansson, S (Johansson, Sverker) ANNUAL REVIEW OF LINGUISTICS, VOL 1 Book Series: Annual Review of Linguistics Volume: 1 Pages: 311-332 DOI: 10.1146/annurev-linguist-030514-124945 Published: 2015


Patagonian Monsters - Cryptozoology, Myths & legends in Patagonia Copyright 2009-2015 by Austin Whittall © 

Saturday, May 30, 2015

Unique Amerindian Genetic Trait


My previous post dealt with the anomalous prevalence of Alzheimer's Disease among American Natives, today's deals with another "unique" Amerindian genetic trait, that extends to what in USA are known as Latinos (people with mixed ancestry that includes Native Americans): one that protects against breast cancer.


Breast Cancer rates by race USA
Breast Cancer incidence by Race USA. From [1]

The table above clearly shows how American Natives and Latinos have the lowest incidence of Breast Cancer among American women.


The cause according to a paper [2] by Laura Fejerman et al.,(2014) is a mutation in chromosome 6: "Here we carry out a genome-wide association study of breast cancer in Latinas and identify a genome-wide significant risk variant, located 5′ of the ​Estrogen Receptor 1 gene (​ESR1; 6q25 region). The minor allele for this variant is strongly protective (rs140068132: odds ratio (OR) 0.60, 95% confidence interval (CI) 0.53–0.67, P=9 × 10−18), originates from Indigenous Americans and is uncorrelated with previously reported risk variants at 6q25."


This mutation is the reason that "Latina women, those with a high proportion of Indigenous American ancestry are at a lower risk of developing breast cancer..." [2].


This mutation must have appeared in America otherwise the purported ancestors of Amerindians (as per the Out of Africa theory) would also carry this variant. By the way, the prevalence of Cancer among Amerindians is almost 1/3 of that found among White American women and half of that found among African American women. The Asian Americans' ratio is also almost twice that of American Natives. (these are supposedly the closest genetic relatives to Amerindians).


Is this also due to a bottleneck? or is did it appear during the "Beringian standstill"?


What does the genome of Neanderthal or Denisova tell us about this mutation? I have tried to find information but have not found anything. It may be a mutation inherited from them. Found only in America.


But what about Papuans, who have a high proportion of Denisovan genes? I found two papers (here) and (here) which inform extremely low levels of cance: roughly 8 to 20 times lower than the ratio among Ameridians"!: from 1958 to 1988, the incidence of breast cancer was betwenn 6.9 and 2.4 per 100,000 women.


Do Papuan women have a genetic mutation that protects them too? or is it just lifestyle? Or are these numbers not adjusted by age?


I found another interesting source (global Cancer atlas) which lists cancer prevalence among all human populations. I selected Breast Cancer Incidence and got this map:



Clearly this differs from the other information: dark blue= EU, Australia, America and NZ, Argentina... countries with a high prevalence of White Europeans that eat beef. And low prevalence in "poor" countries where fatty foods are not so common... Asia, Africa, Bolivia. The quality of the data is also variable, ranging from "A" in the US to "C" in China or "G" in Bolivia (19.2 per 100,000 cases) so it makes me wonder how reliable this information is.


Anway, the intersting point is the mutation in Chromosome 6 found among Native American women.

Sources


[1] Zhang and Olopade in Hereditary Breast Cancer. Edited by Caludine Isaacs, T.Rebbeck. pp.234
[2] Laura Fejerman, et al.,(2014). Genome-wide association study of breast cancer in Latinas identifies novel protective variants on 6q25, Nature Communications 5, Article number: 5260 doi:10.1038/ncomms6260



Patagonian Monsters - Cryptozoology, Myths & legends in Patagonia Copyright 2009-2014 by Austin Whittall © 

Friday, June 13, 2014

mtDNA C1 haplogroup in Europe a Post Script (The X2a hg)


A note to add to my previous post on the mtDNA C1 haplogroup in Europe, and new data regarding X2 haplogroup.


Before her 2014 paper (cited in my post on C1 hg), Der Sarkissian had studied the mtDNA sequenced from Northwestern Russian remains in her 2011 doctorate thesis [1]. Her comments were prescient because in 2014 they were classified as a new hg: C1f; she wrote: "the Uznyi Oleni Ostrov C1 haplotype may in fact represent a distinct European-specific lineage" not linked to the C1 found among Western Siberians.


This Russian C1 was described as "a genetic outlier at the periphery of its proposed origin" (in South Western Central Asia) and its "absence... in other ancient and modern-day European populations suggests that the spread of haplogroup C did not reach further west into central Europe". [1]



She underlines its antiquity when she gives the reason that this haplotype survived for so long: the isolation of this group and maybe, the "closed mating system in isolation with other Mesolithic populations of Scandinavia" [1]


But orthodoxy imposes its imprint on the thesis, and the Amerindian C1b, C1c and C1d lineages are shown as "newer" (the image below shows this clearly) than the "older" Eurasian C1e and C1f lineages from Iceland and the Uznyi Oleni Ostrov site:


The mtDNA C1 haplogroup tree
Phylogenetic tree for C1 mtDNA haplogroup. From [1]

But the really interesting part is that Der Sarkissian points out that another mtDNA haplogroup X2 is very similar to the mtDNA C1 hg in that:


  • It is found at relatively low frequencies in contemporary populations
  • It has a very wide geographic range (from North America to Europe and also Siberia, the Middle East, North Africa and Central Asia)

These similarities suggest a similar evolutionary history for both X2 and C1.


Furthermore X2a (the Amerian clade) split early from the other ones; the split took place in the Middle East and from there the X2a carriers swiftly moved on into Siberia and accessed America in a second migratory wave, not long after the first wave. [2]


The X2 haplogroup


I recall reading about X2 when I was researching for my book (Monsters of Patagonia) back in 2009, and at that time thought that it was most likely due to admixture from contact with Europeans post-1492 discovery of America. This was founded on the idea that it was an Old World haplogroup and that it was only found among certain North American tribes that had been in direct contact with the French and English colonies in Canada and what would later become the US.


Furthermore I was reluctant to engage in further investigations because I found the Solutrean hypothesis as a source for the X2 mtDNA population was rather weak, and some theories regarding ancient Greek admixture into the Cherokees and other North American natives as too flimsy (I omit the Mormon theories and quack Atlanteans as totally non-scientific). There were no serious papers on these subjects and mostly posts in questionable - racist - supremacist forums made me drop further research, until now.


Encouraged by Der Srakissian's thesis I decided to look into the X2 hg once again, and came up with the following details, summarized below: [2][3][4]


X1 haplogroup mtDNA map
mtDNA X haplogroup, range and entry to America. Copyright © 2014 by Austin Whittall

  • Haplogroup X has a wide geographic range covering Europe, North Africa, Asia and North America
  • It descends from the ancient N haplogroup, dating back to at least 30 kya. It evolved from N in the Near East and surrounding areas of Western Eurasia
  • It is currently found at very low frequencies in Europe (less than 5% of all MtDNA)
  • Three populations carry it at high frequencies: Orkney Islanders (7%), Georgians 8%, Druze (11%) -The Druze have the greatest diversity of X lineages of any population X1a, X1c, X2b, X2e, X2f, X2h and X3 and their territory is very likely a refugia of the original X population [4].
  • It is found among Neolithic Europeans at surprisingly high rates: Elau, Germany (4,6 kya), at 22.2%, [5] and 12.5% at Calden, Germany (3000 cal BC), [6]. In these sites all carriers were X2 hg.

  • It is split into two clades, X1 and X2: [2]
    • X1 is found in North and East Africa, with entry routes along the coasts of the Red and Mediterranean seas
    • X2 spans Eurasia and is also found in North American natives (X2a haplotype)
  • X1 is higherst in Africa (36.8% of the X carriers there are X1)
  • X2 prevails in the Middle East, Europe and South Caucasus (97.2% of X hg carriers are X2) and in Central Asia and Siberia (100%)
  • X2a (the Amerindian clade) does not have any close relative in the Old World, including Siberia (Altaian X2e2a is another haplotype which is more recent). Was it lost due to genetic drift?
  • X2a split very early from all other X2 haplotypes in the Middle East, right after X began to expand at the time of the Last Glacial Maximum (LGM)
  • Coalescence time for X2a is 18,000 +⁄- 6,800 ya.
  • X2a occurs only at a 3% frequency among North American Natives, so it is quite uncommon
  • Its range in US and Canada is centered in the Great Lakes and the Western Plains, and has some outliers in Washington State and Arizona. Perego explains this range as caused by a central dispersion corridor from Beringia to the Great Lakes after the ice sheets receded [7]
  • X2a prevails among the Algonquian natives such as the Ojibwe and Chipewa (25% frequency), and is strong among other natives to the West of them: Sioux (15%), Nuu-Chah-Nulth (13%), Navajo (7%), and Yakima(5%). The presence in the Navajo (Southern Na-Dene) is most probably due to recent admixture with other northern Native Americans
  • It has not yet been detected in Central or South America

  • The American haplotypes are: [*]
    ♦X2a1
       - X2a1a: Sioux and Tanoan speakers
         - X2a1a1
       - X2a1b: Ojibwe people
         - X2a1b1
          - X2a1b1a
       - X2a1c: Ojibwe people
    ♦X2a2: Nova Scotia and Newfoundland

Comments


[*] Perhaps there is even more diversity among Amerindians: Perego [7] classified an outlier X2g, that lacked the markers of X2a1 and was different from the other Old World X2 branches, suggesting another extremely rare founder line in America.


An interesting point regarding X's antiquity is "that the basic phylogenetic structures of the [X and U] mtDNA haplogroups in West Eurasia and North Africa are as ancient as the beginning of the spread of anatomically modern humans in this region." [2], which in this paper is dated as 23 - 36 kya, close to the LGM. X is believed to have undergone "a long incubation period coinciding with and following the most recent out of Africa expansion" [4] placing it even further back in time.


Time for my wild hypothesis...


It is old, Neanderthal old. It appeared in the heart of their Eurasian realm. Its current low frequency is due to sucessive overlays of modern human mtDNAs. It was more frequent in the past as shown by the German Neolithic remains. Some refugial areas on the fringes of Europe (Orkney Islands, the Caucasus and the Druze highlands) retained a higher frequency.


The eastern Neanderthals moved on, across Asia following the animals they hunted perhaps long before the H. sapiens OOA move. These Neanderthal peopled the New World. None remained in Siberia that is why it is not found there now. They entered America along the only available corridor open to them reaching the Great Lakes area.


I checked when this corridor was open earlier than 20 kya to provide an entry date into America and came up with the Sangamonian period 125 to 75 kya [8], so it is not so far fetched.


The Neanderthals settled there (perhaps their migration followed specific prey whose range ended there). They never moved on, further South. These were cold-climate people. Later waves of migrants occupied the rest of the New World, sealing these X2a carriers off in their current range.


But... X2 is a Homo sapiens mtDNA haplogroup, not a Neanderthal one. So the theory outlined above is wrong.


Yes, if we accept current timelines for mtDNA evolution. But if we consider that the times are underestimated, that the coalescense time for X2 is not 40 kya but 150 kya and that the African Eve is not so recent, and maybe even found in Eurasia... that perhaps the coalescense leadst to a non sapiens hominin, then it could be possible to accept the scenario outlined above.


I already mentioned something similar regarding the Y chromosome evolution, and am still trying to figure out how to write a post on this subject. The main objection I find is that the real Neanderhtal mtDNA that has been sequenced until now is very different to ours and lies on a distinct phylogenetic branch. Definitively more analysis is needed before I can post on this subject!


Sources


[1] Der Sarkissian, Clio, (2011). Mitochondrial DNA in Ancient Human Populations of Europe Doctorate Thesis Univ. of Adelaide, South Australia.
[2] Maere Reidla et al., (2003). Origin and Diffusion of mtDNA Haplogroup X Am J Hum Genet. Nov 2003; 73(5): 1178–1190. Oct 20, 2003. doi: 10.1086/379380
[3] Europedia, Haplogorup X (mtDNA) www.europedia.com
[4] Shlush LI, Behar DM, Yudkovsky G, Templeton A, Hadid Y, et al., (2008). The Druze: A Population Genetic Refugium of the Near East. PLoS ONE 3(5): e2105. doi:10.1371/journal.pone.0002105
[5] Haak et al., (2008). Ancient DNA, Strontium isotopes, and osteological analyses shed light on social and kinship organization of the Later Stone Age. PNAS November 25, 2008 vol. 105 no. 47 18226-18231 10.1073/pnas.0807592105
[6] Lee, E.J., et al., (2012). Collective burials among agro-pastoral societies in later Neolithic Germany: perspectives from ancient DNA. Journal of Archaeological Science.
[7] Ugo A. Perego et al., (2009). Distinctive Paleo-Indian Migration Routes from Beringia Marked by Two Rare mtDNA Haplogroups. Current Biology Volume 19, Issue 1, 13 January 2009, Pages 1–8. doi: 10.1016/j.cub.2008.11.058
[8] Peter C. Lent, Muskoxen and Their Hunters: A History. pp 18


Patagonian Monsters - Cryptozoology, Myths & legends in Patagonia Copyright 2009-2014 by Austin Whittall © 

Friday, June 6, 2014

mtDNA C1 haplogroup and Neanderthals


In today's post we will let the Y chromosome take a rest for a while because we will be looking into the female contribution to our ancestry, our mitochondrial DNA (mtDNA), and in particular, the interesting distribution of the C1 haplogroup in America and Eurasia.


While I was writing my previous posts on the Y chromosome Q haplogroup in Scandinavia, I came across a paper on the presence of mtDNA haplogroup C1 in Iceland, and recalling that it was considered -until now- an almost exclusively Amerindian haplogroup (with very low frequencies in Asia), I was intrigued, and decided to research the matter. This post is the result.


C1 haplogroup in America


The Native American people belong to five mtDNA haplogroups, which are almost exclusive to America (there have been some minor back-migrations from America into Asia): A2, B2, C1, D1 and X2a.


Of these, haplogroup C1 is widespread across the Americas, from Tierra del Fuego to central northern Canada (it is absent among the Innuit in northernomost Canada and Alaska).

 C1 mtDNA hg map
A Map showing the mtDNA C1 haplogroup current and probable archaic range
Copyright © 2014 by Austin Whittall

C1 hg has in mutated in America and originated four subclades (C1a, C1b, C1c and C1d), of which C1b to C1d are found exclusively in America, and C1a is found in Asia where it back-migrated from the New World. These subclades, in turn have branched into other sublineages.


The Age


The coalescent age of these subclades is shown below [1]:

  • C1a: 7.7 +⁄- 1.9 kya (Siberian Branch)
  • C1a: 18.0 +⁄- 7.9 kya (Founder age)
  • C1b: 17.9 +⁄- 2.3kya
  • C1c: 22.2 +⁄- 3.3 kya
  • C1d: 20.1 +⁄- 4.4 kya

C4 is also present, in Asia and has been recently been detected in two individuals North and South America [1], (C4c) it has a similar age (20 to 25 ky).


I have already written about my doubts regarding the age and coalescence calculations which are based on estimated mutation rates and mtDNA clocks, which I believe are not too reliable (see my post mtDNA clock ticks out of time).


These mutation rates are fit "by hand" by geneticists to coincide with the data provided by the archaeological scientists, which firmly believe in a late peopling of America. So this is a self-fulfilling-prophecy where the mutations found in populations obviously coincide with the arrival dates of those populations in their current territories, since one is based on the other and no external corroboration is provided.


As an example see a criticism againt an "old" age proposed by Fagundes et al., 2008 [4] which states: "The older dates also require additional explanation for the absence of archaeological evidence in the Americas during this phase and for why populations should beshowing significant signals of expansion under such unfavorable climatic conditions" [3], where the unfavorable climate is the last Ice Age however the previous beningn periods are not even considered because they are too old and the archaeological evidence, when provided is not even taken seriously because it is too old!.


Interesingly, C1 has a high values for nucleotide diversity indices, and show a South to North cline (with most variations in South America), indicating that it has deeper roots in the southern part of the New World or that bottlenecks reduced its diversity in the North. In my opinion in points at an older date of entry into America than those mentioned above.


But back to orthodoxy: Just before entering America, there already was intra-haplogroup variation originating the C1b, C1c and C1d subclades [1]. Regarding C1a, it is also found in diverse populations in Asia, but is quite rare there: Southern Siberia where it is found among the Daurs (2.2%), Ulchi (1.1%), Bashkirs (1.5%), Kazakhs (0.8%), Kirghiz (0.5%), Buryat (0.7%), Kalmyk (0.9%), Orok (11.5%), Mongolians (1.3%), Nanai (1.2%) and Japanese (0.3%) [8]. This presence in Asia is the result from a back migration from America [1] or from "the same ancestral population" that originated the Amerindian haplotypes. [7] As additional proof, you will find that several groups mentioned above figure in my post on a back migration of Y chromosome Q hg into Asia, maybe clans with Q and C1a moved back to Asia.


mtDNA C1 haplogroup in Iceland


A Thesis written in 2010 (Sigríður Sunna Ebenesersdóttir) [5], followed by a paper (Sigríður Sunna Ebenesersdóttir et al., 2011) [2] disclosed the presence of a novel C1 haplogroup in Iceland; it was named C1e.


  • It is not the result of recent gene flow from Native Americans or Asians. [2][5]
  • It does not belong to any of the four known Native American (C1b, C1c, and C1d) or Asian (C1a) subclades of haplogroup C1. [2]
  • The Viking settlers in Iceland had brief and bellicose contact with the Native Americans but could have kidnapped women and taken them to Iceland thus originating the local haplogroup C mtDNA lineage, but the differences between Amerindian C1 lineages and the Icelandic one are considerable.
  • Since Aleut, Inuit and Eskimos are not carriers of C1 hg, they are not the vector. [2]
  • C1 is quite infrequent among the North American Na-Dene speaking Native-Americans (Apache, Navajo, Haida and Tlingit). [2]
  • Amerindian haplotypes are very rare in post 1492 Europe, suggesting limited Euro-Amerindian admixture. [2]
  • It is found at very low frequencies in Iceland: about 0.3 %

An Eurasian origin for Iceandic C1e


The likely source arrived in Iceland with the original Viking settlers ca. 900 CE; since these were Europeans, it is possible "that C1e is a very rare European branch". [2] This is corroborated with another line of evidence: "one of the thirteen HVS1 sequences that potentially belong to sub-clade C1e was found in Germany" [2] and that the female settlers brought by the Scandinavian men were women from the British Isles and as "the vast majority of mtDNA lineages observed in contemporary Icelanders are descended from the original set of mtDNA lineages present in the female settlers" [2], this haplogroup was surely present in the Xth century Great Britain.


mtDNA C1 haplogroup in Northern Europe


Only recently was the C1 hg found in the remains of a prehistoric North European (Clio Der Sarkissian et al., 2014) [6], reinforcing the theory of a European source for the Icelandic haplotype. But, surprisingly, it belongs to yet another distinct clade, named C1f, distinct from all other haplotypes.


It was detected in the remains of three individuals retrieved from a Mesolithic site in North Western Russia, on the Kola Peninsula, at the Yuzhnyy Oleni Ostrov site.


This places C1f in Europe 7,500 years ago. But, it has not been detected in current population mtDNA data-bases.


The apparent absence in modern populations may be due to its extinction and replacement by other mtDNA haplogroups introduced by more recent migrations into Europe or a very low frequency among contemporary Europeans leading to its non-detection in the samplings that have been made.


Though C1f has not been found, "HVR-I diversity has revealed extremely low frequencies of hg C1, with very few haplotypes found in Germans, Canarians, Icelanders and Bashkirs. These sequences lack HVR-I Single Nucleotide Polymorphisms (SNPs) diagnostic of the sub-clades C1a (T16356C) and C1d (A16051G)." [6] Meaning that they do not belong to the current East Asian or Amerindian groups (C1a and C1d Hg.)


Comment: The Bashkirs are surely C1a and the Icelanders C1e; the Canarian C1 may be Amerindian: it was a port of call on the way to Southern South America, and had very strong links to the New World during the Spanish colonial period. The German C1 is very probably archaic.


The most widespread haplogroup


So here we have a very interesting mtDNA haplogroup spanning the globe: Northern Europe, Iceland, East - Central Asia ⁄ Siberia and the Americas. What does this tell us?


It apparently entered America via Beringia from Siberia, but it is virtually absent there, where it is believed to have originated as a back-flow from America or an expansion from the ancestral population. It is found in Iceland but the source is apparently European.


It is reasonable to assume that the source for C1 is located in Eurasia (or maybe in America?).


Let's look a the C1f from the Yuzhnyy Oleni Ostrov site. Did they arrive via the invasions of Asian hordes? (we have already seen this hypothesis when we analyzed the Y chromosome Q haplogroup in Europe): Mongols, Huns, Cimmerians (100 BCE to 1,295 CE). It seems unlikely because "the common Asian C1a clade is characterised by the HVR-I transition T16356C, which has not been found in any European C1 haplotype" [6].


The age of these remains (7,500 ya) means that they could not have arisen from European - Native American admixture post-discovery of America in 1492. This clade is definitively an Old World one.


This leaves us with only one option: C1f is very old and has been in Europe at least since Mesolithic times. Its age and location could imply that it is ancestral to the C1e taken by the Vikings (actually by the British women they wed) to Iceland. It also means that C1f and C1a (the East Asian) branches split long ago from the C1 tree, evolving along separate routes. [6] This is shown in the map above where C1f splits from the one leading into America (C1b, C1c, C1d) in Central Asia, and C1a is a back flow from the New World. The pale blue area is the possible range once occupied by the primitive basal C1 root in Eurasia, which later disappeared.


As mentioned above, it has not found in the modern populations in Europe or Asia where it may still exist but has not yet been detected in genetic samplings of the populations. In depth and large scale samples may be required to find it because its originally low frequency may have been further diluted it making it even more uncommon now than it was in the recent past.


To get an idea of its rarity, C1 has appeared only once in Germany, and its presence in Siberia is very low (4 individuals among 1,432 tested) [9]. Interestingly, "The Baltic coast of Europe and Poland also contains a unique C lineage, which may have expanded north from the Black Sea" [9], unfortunately no details are given about it.


The other Mesolithic remains that have been sequenced in Europe did not yield any C1 haplogroup samples [6], this means that even at that time it was quite rare or restricted to certain geographical locations, perhaps as part of relict groups of Paleolithic populations.


And this brings us to... yes! the Neanderthals.


Europe and Central Asia, Western Siberia were the homeland of Neanderthals for hundreds of thousands of years. The Amerindians carry the highest proportion of Neanderthal ancestry suggesting an intimate admixture with them in the New World. The region covered by C1 haplotypes coincides with the range of the Neanderthal people. They were later incorporated by cross-breeding into the modern humans that left Africa 70 kya, this effectively eliminated them by absorption.


But, for this to be true, C1 would have to be a Neanderthal mtDNA haplogroup, and we know (mainstream version) that this is not possible because Neanderthal mtDNA that we have sequenced is too different from ours, furthermore, it would lie on separate branches of the tree, not in one that sprouts from the first modern humans in Africa.


The "Wild" theory


Since this is just a blog and not a peer-reviewed paper and I have no academic career to protect, I can concoct wild ideas and post them here for further criticism and analysis. This is one of them:


The persistence of archaic hominins in modern human genomes


I have already given exactly the same explanation for the Neanderthal's Y chromosome haplogroups which are expected to be different branches, joined at the root by Neanderthal and H. sapiens common ancestor but actually may not be so.


I have expressed my doubts about the ages of the lines and the mutation rates employed to calculate coalescence: maybe mtDNA and Y chromosomes mutate far slower than assumed and the apparent African Modern Humans at the root of the haplo-trees are not human at all, they are H. erectus or H. habilis (the A, B Y chromosome hgs. and the L and M mtDNA lineages within Africa are not the oldest mordern men, they are our ancestors).


This means that the notion of branches splitting like roads and ending in dead-ends is mistaken. Branches criss-cross and mutate and the individuals carrying the mutations change along the branches.


The "tree" below tries to show this, by Analog evolution in (b) I mean many hues and colours due to admixture and introgression, not only discrete lineages that mutate like clocks and die out or survive in a "digital" or binary (black and white, yes - no) fashion, but instead with a full range of options in between).


actual evolutionary tree
An approach to the admixture in human evolution. "Analog" evolution
Copyright © 2014 by Austin Whittall

So the paths we see now out of Africa into the rest of the World are not that of H. sapiens, it is the first Hominids to leave Africa and occupy Asia (the Y chromosome C hg, in India and SE Asia and... maybe even into America) or Europe (H. antecessor, Homo heidelbergensis) and later Neanderthals as they spread out across the Middle East, and Western Eurasia.


Only later do the haplogroups (both female and male) follow the trail of Modern Humans, perhaps the Y Chromosome hg is the into Africa path of the modern Humans that originated out of Africa.


I will polish this theory a little and post on it soon.


The point is that both the Y chromosome Q haplogroup and the mtDNA C1 haplogroup span the same region, are found in low frequencies across Northern Eurasia and America, have been detected also at very low frequencies among Mesolithic people and are now rare in the Old World. Both are absent in Africa. Q is found in Oceania (I have no data regarding C1 there). So both display a similar behavior and (orthodox) time frame hinting at a common origin and source population. Both were later overlain by more recent arrivals, diluting them to near oblivion in the Old World.


To me that spells: Neanderthal admixture and dismissal after encountering modern Humans.


It also means: Neanderthals did reach America and were probably present there at the time of arrival of modern humans (within the last 40 - 50 ky), the encounter led to myths regarding ogres and wid men that persist until nowadays among Native American people.


Sources


[1] Satish Kumar et al., (2011), Large scale mitochondrial sequencing in Mexican Americans suggests a reappraisal of Native American origins. BMC Evolutionary Biology 2011, 11:293
[2] Sigríður Sunna Ebenesersdóttir et al., (2011). A new subclade of mtDNA haplogroup C1 found in icelanders: Evidence of pre-columbian contact?. Am. J. Phys. Anthropol., 144: 92–99. doi: 10.1002/ajpa.21419
[3] Simon Y.W. Ho and Phillip Endicott, Letter. The Crucial Role of Calibration in Molecular Date Estimates for the Peopling of the Americas. The American Journal of Human Genetics 83, 127–147, July 2008 pp. 142
[4] Fagundes, N.J., et al., (2008). Mitochondrial population genomics supports a single pre-Clovis origin with a coastal route for the peopling of the Americas. Am. J. Hum. Genet. 82, 583–592.
[5] Sigríður Sunna Ebenesersdóttir (2010). Faculty of Social Science. MA-thesis, Anthropology. The origin of Icelandic mtDNA lineages from haplogroup C
[6] Clio Der Sarkissian et al., (2014). Mitochondrial Genome Sequencing in Mesolithic North East Europe Unearths a New Sub-Clade within the Broadly Distributed Human Haplogroup C1. PLoS One. 2014; 9(2): e87612. Feb 4, 2014. doi: 10.1371/journal.pone.0087612
[7] Tamm E, Kivisild T, Reidla M, Metspalu M, Smith DG, et al., (2007). Beringian Standstill and Spread of Native American Founders. PLoS ONE 2(9): e829. doi:10.1371/journal.pone.0000829
[8] Derenko M, Malyarchuk B, Grzybowski T, Denisova G, Rogalla U, et al., (2010). Origin and Post-Glacial Dispersal of Mitochondrial DNA Haplogroups C and D in Northern Asia. PLoS ONE 5(12): e15214. doi:10.1371/journal.pone.0015214
[9] Jeremy R. Newton, (2011). Ancient Mitochondrial DNA From Pre-historic Southeastern Europe: The Presence of East Eurasian Haplogroups Provides Evidence of Interactions with South Siberians Across the Central Asian Steppe Belt. Master Thesis Paper 5.
 

On the 70th anniversary of D-Day. Long live the heroes of that glorious day, who layed down their lives for freedom.


Patagonian Monsters - Cryptozoology, Myths & legends in Patagonia Copyright 2009-2014 by Austin Whittall © 

Wednesday, May 14, 2014

Alcohol, genes and human migrations... Part 3


In two previous posts (Part 1 and Part 2) we looked into the Alcohol and Aldehyde Dehydrongenase (ADH and ALDH respectively) enzimes that metabolize alcohol in humans.


We noticed that they appear in all human populations but, in different genetic variations, which seem to be distributed globally following certain dispersal routes, acquiring higher frequencies among some peoples while in others they are absent or found at lower frequencies.


These variations in genes in turn affect how these people process their alcoholic intake. Some may have very ancient origins while others seem to be quite recent. Today we will present the final data and complete this third and last post of this series.


ADH and orthodoxy


A paper that is now 11 years old (Mulligan et al., 2003) [1] types Alcohol Dehydrogenase (ADH) and looks into the differente alleles for various populations. As expected, these are found in different frequencies for ADH1C / ADH1B among Amerindians, Asians and Africans (other populations were not included in this paper).


I was surprised at how the authors "edited" their data: (Bold mine) [1]


"For each of the five studied populations, all inferred haplotypes were removed if they did not significantly improve the model as assessed by a log likelihood ratio. Based on this criterion, the following numbers of unconfirmed haplotypes were removed from each population: American Indian, 3; Siberian, 2; Mongolian, none; Chinese, none; Nigerian, none.
The American Indian population had more unconfirmed haplotypes than the others, most likely because it had the largest sample size and contained relatives. However, all of the unconfirmed haplotypes were rare and increased the likelihood of particular individuals only trivially."


They used a program (MLOCUS) which conducts a probabilistic analysis and assigns log likelihood values, so as we can see above, they "removed... haplotypes" because they "did not significantly improve the model" or "increased the likelyhood... only trivially" [1].


Rare Amerindian haplotypes were therefore discarded (and in a high proportion compared to other populations), this surely biased the outcome, moreso since their impact on the "model" was minimum.


Then we must add the assumption that African and Eurasian genes are much older than Native American ones:


The assumption that Amerindians are "young"


Mulligan et al., conclude "No evidence of recombination was detected at the ADH or ALDH loci in the American Indian population. One Chinese and three Nigerian ADH haplotypes appear to have arisen by recombination and/or gene conversion, a result that is consistent with a deeper evolutionary history in these populations compared with American Indians." [1]


The fact is that the Chinese recombination is the one that originates Ht 6 affecting 8% of the Chinese population. It is not "deep" (i.e. old, archaic, ancient), actually this Ht6 "possessed the ADH1B*47His allele" which, as we have seen (Part 2 of this post) is very recent among Chinese:

Hui Li, et al., 2011 [2] gives the following dates for the ADH1B*47His alleles (this paper's nomenclature for them is H6 and H7): "The estimated ages of H6 and H7 both indicate relatively recent coalescents or expansion times of the haplogroups.The age of H7 is estimated at only around 2.8 thousand years... This young age is unexpected..." [2]


Clearly recent, so why do Mulligan et al. asume that the allele is "ancient"? [1]


I believe that they are trying to fit the paper to adjust to the current orthodoxy of a late peopling of America, therefore Asian lineages must be ancient and Amerindian ones young.


To do so, they also "manually" fit the Ht 7 found in Africans (Nigerians), which they believe to be the "ancestral" haplotype, between two Amerindian alleles, suggesting it is the most parsimonious setting for it; then they derive both Amerindian alleles, Ht 2 and Ht 3, from it; the write (my comments bold between brackets) [1]


The order of ADH1C HaeIII and ADH1C Ile349Val [that is, how to get from Ht3 to Ht2] could not be determined based solely on the American Indian data because of complete cosegregation of these markers [cosegregation: the genes and markers are inherited together]. However, Ht 7 in the Nigerians fit the cladogram most parsimoniously between Hts 2 and 3, which placed ADH1C Ile349Val after ADH1C HaeIII when moving outward in the cladogram....
Alternatively, Osier et al. (2002) inferred a haplotype in two American Indian populations that would reverse the order of ADH1C HaeIII and ADH1C Ile349Val.
[exactly the opposite to what Mulligan et al. suggest!] Osier et al. (2002) also inferred five additional ADH haplotypes present at low frequencies in four American Indian populations. Two of Osier and co-worker’s (2002) haplotypes, including the one that would reverse the order of ADH1C HaeIII and ADH1C Ile349Val, were removed from our dataset [they deliberately removed the data that contradicted their assumption] based on insignificant improvement of the model, suggesting that a more minimal set of haplotypes may exist for the populations investigated in Osier et al. (2002). [1]


What did Ossier et al. find?


Since Mulligan et al., mentioned Ossier et al., 2002, [3] we will take another look at Ossier & team's work (basically Table 4 and pp. 95):


Ossier et al., defined an Ancestral haplotype (212111) [corresponding to Ht 2 in Mulligan et al.], found in all populations aorund the world, with some minor exceptions, at relatively low frequencies (those with the highest value are shown in brackets): Africans: 0 - 10.6%, Europeans: 0.7 - 30.7% [Finns], East Asia: 0 - 9.8%, Pacific-PNG: 14.6 - 38%, Siberia: 13.1%, N. America: 11.7 - 48.1% [Mexican Pima], S. America: 3.2 - 10.8%.


I wonder why do Finns and Mexican Pima have such high frequencies


The Ancestral haplotype then mutated into two alleles:


  • 112111 [Ht 1 in Mulligan et al.] This is the ADH1C HaeIII site-absent allele, and it differs from the ancestral haplotype only at the ADH1C EcoRI site. (it is what Mulligan et al. named Ht1), which is found in most populations around the world and very common in Europe: Africa: 2.8 - 17.2%, Europe: 5.0 - 30.8% [Basque], East Asia: 0 - 14%, nil in Pacific - PNG, Siberia: 14%, N. America: 2.3 - 21%, S. America: 6.9 - 22.7%
  • 211111 [Ht 7]. Originated by "an independent mutation of the ADH1C Ile349Val site on the ancestral haplotype... This haplotype is rarely seen today but is present in the !Kung San (8.6%), Biaka Pygmies (10.8%), and African Americans (1.2%)". Some outliers: Yakut 1.3%, Micronesians 3%, Danes 1%, Irish 0.8%, San Francisco Chinese 1%. Zero elsewhere.
  • 221111 [Ht 3], is the mutation of 211111 and is "most common around the world" :
    Africa: 35.7 - 87.5%, Europe: 1.9 - 39%, East Asia: 9,4 - 20.5%, Pacific - PNG: 23.4 - 42.3%, Siberia: 42.4%, N. America: 28.6 - 68.3%, S. America: 64.9 - 82.3%. Note the very high frequencies in South America compared to much lower values in Asia - Siberia.

Who is correct? Mulligan or Ossier? You can decide based upon the evidence, please check both papers.


Unsurprisingly Mulligan et al. hint that the "difference in haplotype distribution may reflect the fact that different Asian and African populations were analyzed by Osier et al. (2002)." They also recognize that founder effects and possible population bottlenecks may have influenced Amerindian haplotype frequencies.[1]


Amerindian oddities


Nevertheless, the striking facts are that American Indians have, for both Mulligan and Ossier some peculiarities:

  1. The highest frequency of Ht 2 in the whole world (this is the Ancestral allele)
  2. The highest frequency of Ht 1 in the world (and this is only one mutation away from the ancestral allele, so it is evidently "old" too)
  3. The highest frequency of Ht 3 in the world if we consider only South American Natives (78.4%) or second highest 62.3% (for both North and South Amerindians) vs. 65.1% for Sub Saharan Africans. This is the most common allele worldwide, yet its highest frequency is found in Africa -cradle of Mankind- and... of all places, America!

An explanation is that a bottleneck effect in America eliminated some alleles leaving others, which later expanded to fill the void, hence a larger frequency of some alleles in comparison to the rest of the world.

I find this difficult to believe because there are some extremely rare alleles are present in America which are only found in Africa and in the Pyrenean foothills in Spain. A bottleneck would have eliminated these too, how did they survive? Were they present in even larger numbers before the bottleneck? Do we see the imprint of a once larger population? (I do believe that European contact in the 1500s wiped out a large number of alleles unique to Amerindians. So the "lack of diversity" does not mean a "recent" origin of Amerindians, it is merely the outcome of attrition due to disease and war).


Below are some Rare alleles and their frequencies [3]:


  1. 111111: 1.1% Karitiana, 9.2% Maya, 1.1% Arizona Pima. While in the rest of the world it is only found among: Basque 1.6%, North Moroccans 2.2%, !Kung San 2.3% and S.E. Bantu speakers: 1.4%. Zero in Asia, Siberia and the rest of the world.
  2. 121111: 1.1% Karitiana, 1.5% R. Suri, and (again) 1.6% Basque, 0.7% Catalans, 0.6 - 8.9% North Africans, !Kung San 2.6% and S.E. Bantu speakers: 4.2%. Zero in the rest of the world.

We could argue that Spanish genes admixed with those of Amerindian after the discovery of America: this would account for Catalan and Basque alleles. Additionally Moroccan genes surely got into the Spanish genome during the Moorish occupation of Spain (711 - 1491 C.E.), but, what about the Sub Saharan Africans? Did slave trade introduce !Kung San genes into America? I find it unlikely. Actually you would expect other African genes but not !Kung San genes.


Now, since Ht 1, Ht 2 (ancestral allele) and Ht 3 are all found in Africa you might expect them to have originated there. But the !Kung San do not carry Ht 1 and Sub Saharan Africans frequency for it is very low (6.1%), but not so in North Africa (13.6%) or Middle East (12%) so perhaps it originated out of Africa and back-migrated later, skipping East Asia and Siberia which also have low frequencies (3.7%), it is absent in PNG and Micronesia, but remained strong in America (11.8%) and in Europe (27.3%) where it probably originated.


Could they be a Denisovan allele? Not likely since it is not found among Papuans and they have the highest Denisovan admixture.


Perhaps it is Neanderthal. If so, its low rate among East Asians (which should have a very high Neanderthal admixture) is easily explained due to the exponential growth of the recent Ht 6 and Ht 7 haplotypes in that area, which were positively selected at the expense of the other alleles.


Closing Comments


As a summary of this "three part" post, I will highlight two things:


First; there is a tendency to "fit" the data to corroborate the orthodox theory of a late peopling of America by a small group of people with limited genetic diversity (founder effect and bottleneck). These then expanded in the New World filling it with people with a very different mix of genes than those found in the Old World.


This is akin to Astronomy before the "Big Bang" theory (the age of the Universe and the cosmological constant were "adjusted" to fit the prevailing theories) or Geology before Plate Tectonics.


Second, the different alleles found among American natives (and this is even more noticeable among South American natives, since North American ones have the imprint of a recent Asian migratory wave) are not similar to those found in East Asia. Some appear to be more similar to those of Caucasians or Africans than to those of Asians, which is unusual since one would expect Amerindians to resemble their supposed Asian ancestors.


Post discovery admixture, bottlenecks and founder effects are used to explain away these differences, but it is highly probable that a stronger archaic admixture is found among Amerindians than elsewhere. Probably due to an Admixture that took place in America, during a peopling event that predated the appearance of Modern East Asians or Siberians.


Part 1

Part 2


Sources


[1] Connie J. Mulligan, et. al., (2003). Allelic variation at alcohol metabolism genes (ADH1B, ADH1C, ALDH2) and alcohol dependence in an American Indian population. Hum Genet (2003) 113 : 325–336 doi: 10.1007/s00439-003-0971-z

[2] Hui Li, et al., (2007). Geographically Separate Increases in the Frequency of the Derived ADH1B*47His Allele in Eastern and Western Asia. Am. J. Hum. Genet. 2007;81:842–846. doi: 10.1086/521201
[3] Michael V. Osier, Andrew J. Pakstis, David Goldman, Howard J. Edenberg, Judith R. Kidd, and Kenneth K. Kidd., (2002). A Proline-Threonine Substitution in Codon 351 of ADH1C Is Common in Native Americans. doi: 10.1097/01.ALC.0000042013.13899.75, Alcohol Clin Exp Res, Vol 26, No 12, 2002: pp 1759–1763



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