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Offline BabylonianJew

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Racial Admixture in various European Populations
« on: May 15, 2007, 01:01:12 PM »
Greeks have Negroid admixture and Mongoliod(Turks): SAHARAN GENES IN GREECE

The first major study of gene frequencies in Greece, Macedonia and Crete was completed in December 2000, titled "HLA genes in Macedonians and the sub-Saharan origin of the Greeks",and published by the journal "Tissue Antigens" that year.

http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=11260506&dopt=Abstract
 
   Tissue Antigens February 2001, vol. 57, no. 2,   pp. 118-127
 
HLA genes in Macedonians and the sub-Saharan origin of the Greeks

A. Arnaiz-Villena; K. Dimitroski; A. Pacho; J. Moscoso; E. Go´mez-Casado; C. Silvera-Redondo; P. Varela; M. Blagoevska; V. Zdravkovska; J. Martý´nez-Laso

Department of Immunology and Molecular Biology, H. 12 de Octubre, Universidad Complutense, Madrid, Spain.

 

HLA alleles have been determined in individuals from the Republic of Macedonia by DNA typing and sequencing. HLA-A, -B, -DR, -DQ allele frequencies and extended haplotypes have been for the first time determined and the results compared to those of other Mediterraneans, particularly with their neighbouring Greeks. Genetic distances, neighbor-joining dendrograms and correspondence analysis have been performed. The following conclusions have been reached: 1) Macedonians belong to the "older" Mediterranean substratum, like Iberians (including Basques), North Africans, Italians, French, Cretans, Jews, Lebanese, Turks (Anatolians), Armenians and Iranians, 2) Macedonians are not related with geographically close Greeks, who do not belong to the "older" Mediterranenan substratum, 3) Greeks are found to have a substantial relatedness to sub-Saharan (Ethiopian) people, which separate them from other Mediterranean groups. Both Greeks and Ethiopians share quasi-specific DRB1 alleles, such as *0305, *0307, *0411, *0413, *0416, *0417, *0420, *1110, *1112, *1304 and *1310. Genetic distances are closer between Greeks and Ethiopian/sub-Saharan groups than to any other Mediterranean group and finally Greeks cluster with Ethiopians/sub-Saharans in both neighbour joining dendrograms and correspondence analyses. The time period when these relationships might have occurred was ancient but uncertain and might be related to the displacement of Egyptian-Ethiopian people living in pharaonic Egypt.

 




Fig. 2. Correspondence analysis showing a global view of the relationship between Mediterraneans and sub-Saharan and Black African populations according to the HLA allele frequencies in three dimensions (bidimensional representation). HLA-DRBI allele frequencies data.

 



Fig. 3. Correspondence analysis showing a global view of the relationship among West Mediterraneans (green), East Mediterraneans (orange), Greeks and sub-Saharan populations (red) and Blacks (grey) according to HLA allele frequencies in three dimensions (bidimensional representation). HLA-DR and DQ (low resolution) allele frequencies data.

Table 5 shows the presence of these Greek alleles mainly in sub-Saharan populations from Ethiopia (Amhara, Oromo), Sudan (Nuba) and West Africa (Rimaibe, Fulani, Mossi).

It may be deduced from these data that sub-Saharans and Greeks share quasi-specific HLA-DRB1 alleles. The neighbor-joining tree (Fig. 1) and the correspondence analyses (Figs 2 and 3) confirm this Greek/sub-Saharan relatedness. The HLA-DRB1 genetic distances between Greeks and other Mediterraneans are shown in Table 6 and also support a sub-Saharan/Greek relatedness; genetic distances with HLA-DR and -DQ generic typings (not shown) give essentially the same results.

Our results show that Macedonians are related to other Mediterraneans and do not show a close relationship with Greeks; however they do with Cretans (Tables 3, 4, Figs 1–3). This supports the theory that Macedonians are one of the most ancient peoples existing in the Balkan peninsula, probably long before arrival of the Mycaenian Greeks (10) about 2000 B.C. Other possible explanation is that they might have shared a genetic background with the Greeks before an hypothetical admixture between Greeks and sub-Saharans might have occurred.

Much to our surprise, the reason why Greeks did not show a close relatedness with all the other Mediterraneans analyzed (Tables 5, 6 and Figs 1–3) was their genetic relationship with sub-Saharan ethnic groups now residing in Ethiopia, Sudan and West Africa (Burkina-Fasso). Although some Greek DRB1 alleles are not completely specific of the Greek/sub-Saharan sharing, the list of alleles (Table 5) is self-explanatory. The conclusion is that part of the Greek genetic pool may be sub-Saharan and that the admixture has occurred at an uncertain but ancient time.

Thus, it is hypothesized that there could have been a migration from southern Sahara which mixed with ancient Greeks to give rise to a part of the present day Greek genetic background. The admixture must have occurred in the Aegean Islands and Athens area at least. 

Also, the time when admixture occurred could be after the overthrown of some of the Negroid Egyptian dynasties (Nubian or from other periods) or after undetermined natural catastrophes (i.e.: dryness).

(Full text in PDF format available here.)
 

(A study of how HLA Alleles are race specific can be found here)


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MONGOLOID MARKER IN GREECE

A recent study of mtDNA in Greece revealed the presence of the HpaI morph 1 sequence, which is a Mongoloid marker, introduced either through slavery or the mixed race Ottoman occupation.

http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=7916320&dopt=Abstract
 

 
1: Hum Biol. 1994 Aug;66(4):601-11.
Mitochondrial DNA polymorphism in northern Greece.
Astrinidis A, Kouvatsi A.

Department of Genetics, Development, and Molecular Biology, School of Biology, Aristotle University of Thessaloniki, Greece.

The polymorphism of human mitochondrial DNA (mtDNA) was studied in 118 unrelated Greeks (from northern Greece) using total blood cell DNA and the restriction enzymes HpaI, BamHI, HaeII, MspI, AvaII, and HincII. One new morph was identified for MspI (named MspI morph 18Gr) and is the result of a mutation in a previously thought monomorphic site at 104 bp. HpaI morph 1 was detected for the first time in a European sample. Also, AvaII morph 13 was observed in Greece in a frequency higher (5.93%) than that found in any other population. Eighteen mtDNA types were identified, three of which are new [86-2 (1-3-1-4-9-2), 87-2 (2-3-1-1-13-2), and 88-2 (2-1-1-18Gr-1-2)] and can be derived from already known mtDNA types by single restriction site changes. Type 57-2 (2-3-1-4-13-2), which had been previously characterized as "Italian," was found with higher frequency (4.24%) in northern Greece. The calculation of genetic distances and chi-square values through Monte Carlo simulation shows that the Greek sample does not differ from the Italian sample.
PMID: 7916320 [PubMed - indexed for MEDLINE]
 


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AFRICAN BLOOD GROUPS IN GREECE

"As usual in the Mediterranean area CDe is high, and cDe, presumably from African admixture, reaches about 6 per cent." (p73)

Cyprus: ". . . the presence of over 5 per cent cDe suggests African immigration." (p73)
Source: Mourant AE, Kopéc AC, Domaniewska-Sobczak K. The distribution of the human blood groups and other polymorphisms. London, Oxford University Press, 1976.
 


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28% MIDDLE EASTERN HAPLOGROUP HG9 IN GREECE

According to a study conducted by Lluís Quintana-Murci et. al.. and published in The American Journal of Human Genetics, (Volume 68, 2001, pages 537-542), the Middle Easter Haplogproup HG9 runs at 28% in Greece.

http://www.journals.uchicago.edu/AJHG/journal/issues/v68n2/002418/002418.html
Am. J. Hum. Genet., 68:537-542, 2001


 
Y-Chromosome Lineages Trace Diffusion of People and Languages in Southwestern Asia
Lluís Quintana-Murci,1 Csilla Krausz,1 Tatiana Zerjal,2 S. Hamid Sayar,3 Michael F. Hammer,4 S. Qasim Mehdi,5 Qasim Ayub,5 Raheel Qamar,5 Aisha Mohyuddin,5 Uppala Radhakrishna,6 Mark A. Jobling,7 Chris Tyler-Smith,2 and Ken McElreavey1
. . .

HG 9, defined by the 12f2 deletion, is largely confined to caucasoid populations, with its highest frequencies being found in Middle Eastern populations.

In Iranian populations, HG 9 shows very high frequencies (30%60%). Populations from the southeastern Caspian region and the Zagros Mountains exhibit the highest frequencies so far observed (60%). High frequencies of HG 9 have been found throughout the Fertile Crescent region (Hammer et al. 2000): Palestinians, 51%; Lebanese, 46%; and Syrians, 57%. The incidences of HG 9 in Pakistan (18%) and northern India (19%) indicate a decreasing-frequency cline from Iran toward India.

Table 1
Frequency Distribution of HG 9 and HG 3 in Human Populations from Different Regions

REGIONa  N FREQUENCYb
(%) SOURCE
HG 9 HG 3
Iran:c
 
 
 
 
     Azarbaijan 83 34 17 Present study
     Zagros Mountains 34 59 6 Present study
     Western Caspian 32 53 3 Present study
     Eastern Caspian 25 56 20 Present study
     Tehran region 50 30 14 Present study
     Central-north 79 39 9 Present study
     Central-south 72 38 17 Present study
     Eastern provinces 26 35 31 Present study
Pakistan 708 18 32 Present study
India:
 
 
 
 
     Gujurat 58 19 26 Present study
     Jaunpur 152 NT 20 Zerjal et al. (1999)
     Indians mixed 72 NT 15 Hammer et al. (1998)
     Uttar Pradesh 62 7 NT Semino et al. (1996)
Sri Lanka 83 NT 15 Hammer et al. (1998)
Middle East:
 
 
 
 
     Lebanon 24 46 4 Hammer et al. (2000)
     Syria 91 57 9 Hammer et al. (2000)
     Palestine 73 51 0 Hammer et al. (2000)
Europe:
 
 
 
 
     Turkey 167 33 5 Rosser et al. (2000)
     Russia 122 4 47 Rosser et al. (2000)
     Ukraine 27 0 30 Rosser et al. (2000)
     Latvia 34 0 41 Rosser et al. (2000)
     Poland 112 4 54 Rosser et al. (2000)
     Greece 36 28 8 Rosser et al. (2000)
     Italy 99 20 2 Rosser et al. (2000)
     Spain 126 3 2 Rosser et al. (2000)
Africa:
 
 
 
 
     Algeria 27 41 0 Rosser et al. (2000)
     Sub-Saharan Africa 199 1 0 Hammer et al. (2000)
 

Offline BabylonianJew

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Re: Racial Admixture in various European Populations
« Reply #1 on: May 15, 2007, 01:02:19 PM »
The Anglo-Saxons have Indian(India) blood: RACIAL MIXING BROUGHT THE HEMOGLOBIN D DISORDER TO BRITAIN AND IRELAND

Hemoglobin D is a genetically transmitted blood disorder which originated on the Indian sub-continent, and which spread to England, Scotland and Ireland during the colonial period when many soldiers – Englishmen, Scots and Irishmen – took Indian wives back to their homelands.

It is worthwhile to review the hemoglobin D case study because it proves two things:

- Firstly, that genetically inherited conditions, such as sickle cell and hemoglobin D, are transmitted directly by racial mixing; and

-Secondly, to show that it is not just southern Europe that has been affected by racial mixing during the course of history, but that northern European lands have also fallen prey to this phenomenon, albeit in smaller overall numbers.

 HEMOGLOBIN TYPE IS INHERITED

“HEMOGLOBIN is the oxygen transporting substance found in the red blood cells. There are hundreds of different hemoglobin variants identified in all races and populations of people. The kind of hemoglobin we have depends upon our genetic inheritance. Genes are units of inheritance passed on from our parents. These messengers determine characteristics such as eye and hair color, and they also determine hemoglobin type.” - The Virginia Sickle Cell Awareness Program (VASCAP), http://views.vcu.edu/pediatrics/vascap/fast_facts/HemoD.PDF
 
 
 “Most people have the type of hemoglobin called hemoglobin A (also called normal or adult hemoglobin). However there are many different types of hemoglobin found in people throughout the world. Hemoglobin D is one type; sickle hemoglobin is another type.”- University of Rochester Medical Center, Division of Genetics, http://www.urmc.rochester.edu/genetics/brochures/pdf/hbdbro1.pdf
 

 COMPLICATIONS ARISING FROM HEMOGLOBIN D

Carriers of hemoglobin D are at little risk themselves, but if they should have children with other carriers, there is a 25 percent chance that their children will have either sickle cell disease, or milder variants known as hemoglobin SD or just be carriers of the trait.

The University of Rochester’s Medical Center, Division of Genetics, explains it this way:

“If you and your partner have hemoglobin D trait, there is a 25% chance with each pregnancy that your child will inherit both hemoglobin D genes and have homozygous hemoglobin D. Homozygous hemoglobin D is not associated with health problems.

You should not be concerned for your own health, but if your partner has sickle cell trait, there is  a 25% chance with each pregnancy that your child will have hemoglobin SD disease, which can be serious.

A person with hemoglobin SD disease may suffer from anemia and bouts of pain called crises. These crises can occur without warning, affect any part of the body and last hours or days. There may also be problems with frequent infections and unexplained fevers. Daily doses of penicillin and folic acid are required.”- University of Rochester Medical Center, Division of Genetics, http://www.urmc.rochester.edu/genetics/brochures/pdf/hbdbro1.pdf
 

RACIAL LINK TO INCIDENCE OF HEMOGLOBIN D

“Hemoglobin D is uncommon in North America, occurring in less than 1 of 5000 persons. In the Punjab region of India and Pakistan, approximately 3 percent of the populations have the hemoglobin D Trait. This trait is more common in people of English, Irish, or Scotch ancestry than in those of other ethnic groups.” - The Virginia Sickle Cell Awareness Program (VASCAP), http://views.vcu.edu/pediatrics/vascap/fast_facts/HemoD.PDF
 
 
“Hemoglobin D is found in people whose ancestors come from Pakistan and Northwestern India and occasionally Europeans, especially the British and Irish” – University of Rochester Medical Center, Division of Genetics, http://www.urmc.rochester.edu/genetics/brochures/pdf/hbdbro1.pdf
 

 HEMOGLOBIN D CAME TO BRITAIN WITH RACIAL MIXING

“This trait is more common in people of English, Irish or Scotch ancestry than in those of other ethnic groups. The high frequency of hemoglobin D Trait in this population is believed to reflect the large number of Indian wives brought home to England by British troops during Britain's long occupation of India.” - The Virginia Sickle Cell Awareness Program (VASCAP), http://views.vcu.edu/pediatrics/vascap/fast_facts/HemoD.PDF
 

The proof is thus clear that during the colonial era, (circa 1850 -1950) racial mixing between soldiers in the British Army and Indians took place. Like sickle cell disease, Hemoglobin D was transferred to a White population through interracial contact.


Offline BabylonianJew

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Re: Racial Admixture in various European Populations
« Reply #2 on: May 15, 2007, 01:03:41 PM »
Racial admixture in Slavs Mongoloid blood:  chromosomal heritage of Croatian population and its island isolates
Lovorka Bara, Marijana Peri, Irena Martinovi Klari, Siiri Rootsi, Branka Janiijevi, Toomas Kivisild, Jüri Parik, Igor Rudan, Richard Villems and Pavao Rudan

Y chromosome variation in 457 Croatian samples was studied using 16 SNPs/indel and eight STR loci. High frequency of haplogroup I in Croatian populations and the phylogeographic pattern in its background STR diversity over Europe make Adriatic coast one likely source of the recolonization of Europe following the Last Glacial Maximum. The higher frequency of I in the southern island populations is contrasted with higher frequency of group R1a chromosomes in the northern island of Krk and in the mainland. R1a frequency, while low in Greeks and Albanians, is highest in Polish, Ukrainian and Russian populations and could be a sign of the Slavic impact in the Balkan region. Haplogroups J, G and E that can be related to the spread of farming characterize the minor part (12.5%) of the Croatian paternal lineages. In one of the southern island (Hvar) populations, we found a relatively high frequency (14%) of lineages belonging to P*(xM173) cluster, which is unusual for European populations. Interestingly, the same population also harbored mitochondrial haplogroup F that is virtually absent in European populations - indicating a connection with Central Asian populations, possibly the Avars.
 


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http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=3056831&dopt=Abstract

 
1: Hum Genet. 1988 Nov;80(3):207-18
Characteristics of Mongoloid and neighboring populations based on the genetic markers of human immunoglobulins.

Matsumoto H.

Department of Legal Medicine, Osaka Medical College, Japan.

Since the discovery in 1966 of the Gm ab3st gene, which characterizes Mongoloid populations, the distribution of allotypes of immunoglobulins (Gm) among Mongoloid populations scattered from Southeast Asia through East Asia to South America has been investigated, and the following conclusions can be drawn: 1. Mongoloid populations can be characterized by four Gm haplotypes, Gm ag, axg, ab3st, and afb1b3, and can be divided into two groups based on the analysis of genetic distances utilizing Gm haplotype frequency distributions: the first is a southern group characterized by a remarkably high frequency of Gm afb1b3 and a low frequency of Gm ag, and the second, a northern group characterized by a high frequency of both Gm ag and Gm ab3st but an extremely low frequency of Gm afb1b3. 2. Populations in China, mainly Han but including minority nationalities, show remarkable heterogeneity of Gm allotypes from north to south and contrast sharply to Korean and Japanese populations, which are considerably more homogenous with respect to these genetic markers. The center of dispersion of the Gm afb1b3 gene characterizing southern Mongoloids has been identified as the Guangxi and Yunnan area in the southwest of China. 3. The Gm ab3st gene, which is found with its the highest incidence among the northern Baikal Buriats, flows in all directions. However, this gene shows a precipitous drop from mainland China to Taiwan and Southeast Asia and from North to South America, although it is still found in high frequency among Eskimos, Koryaks, Yakuts, Tibetans, Olunchuns, Tungus, Koreans, Japanese, and Ainus. On the other hand, the gene was introduced into Huis, Uyghurs, Indians, Iranians, and spread as far as to include Hungarians and Sardinians in Italy. On the basis of these results, it is concluded that the Japanese race belongs to northern Mongoloids and that the origin of the Japanese race was in Siberia, and most likely in the Baikal area of the Soviet Union.

PMID: 3056831 [PubMed - indexed for MEDLINE]
 
 

Offline BabylonianJew

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Re: Racial Admixture in various European Populations
« Reply #3 on: May 15, 2007, 01:06:43 PM »
Racial mixing in Italians: Joining the Pillars of Hercules: mtDNA Sequences Show Multidirectional Gene Flow in the Western Mediterranean
S. Plaza, F. Calafell, A. Helal, N. Bouzerna, G. Lefranc, J. Bertranpetit and D. Comas

Phylogenetic analysis of mitochondrial DNA (mtDNA) performed in Western Mediterranean populations has shown that both shores share a common set of mtDNA haplogroups already found in Europe and the Middle East. Principal co-ordinates of genetic distances and principal components analyses based on the haplotype frequencies show that the main genetic difference is attributed to the higher frequency of sub-Saharan L haplogroups in NW Africa, showing some gene flow across the Sahara desert, with a major impact in the southern populations of NW Africa.

Each of the subregions analysed (NW Africa and SW Europe) shows sequences that originated on the opposite shore of the Mediterranean. This is particularly clear in the case of U6 and L in SW Europe. L sequences are found at frequencies 3% in Iberia and 2.4% in Italy. Given the relatively high frequencies of L sequences in NW Africa, it is not clear whether they were contributed by the historical populations movements from the south to the north of the Mediterranean (such as the Moslem invasions of the 7th-11th centuries), or whether its presence is associated with other processes not directly linked to NW Africa.

Three Italian L sequences have been described throughout Africa, and the remaining five are not found in >1,000 sub-Saharan individuals. Thus, the presence of L sequences cannot be attributed to migration from NW Africa, and may instead represent gene flow from other sources, such as the Neolithic expansion or the Roman slave trade.

Full article can be found cached here.
 


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 AFRICAN ANCESTRY IN SICILY

http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=103355&dopt=Abstract
 

 
Blood group phenotypes and the origin of sickle cell hemoglobin in Sicilians.
Sandler SG, Schiliro G, Russo A, Musumeci S, Rachmilewitz EA.
 

As an approach to investigating the origin of sickle cell hemoglobin (hemoglobin S) in white persons of Sicilian ancestry, two groups of native Sicilians were tested for blood group evidence of African admixture. Among 100 unrelated Sicilians, the phenotypes cDe(Rho) and Fy(a-b-), and the antigens V(hrv) and Jsa, which are considered to be African genetic markers, were detected in 12 individuals. Among 64 individuals from 21 families with at least one known hemoglobin S carrier, African blood group markers were detected in 7 (11%). These findings indicate that hemoglobin S is only one of multiple African genes present in contemporary Sicilian populations. The occurrence of hemoglobin S in white persons of Sicilian ancestry is considered to be a manifestation of the continuing dissemination of the original African mutation.

PMID: 103355 [PubMed - indexed for MEDLINE]
 

 

http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=7365760&dopt=Abstract
 

 
Sickle cell disease in Sicily.
Roth EF Jr, Schiliro G, Russo A, Musumeci S, Rachmilewitz E, Neske V, Nagel R.

The chemical and physical properties of haemoglobin S derived from homozygotes for this haemoglobin in Sicily were examined, as well as some erythrocytic characteristics. Sicilian Hb S was identical to that found in USA black patients in electrophoretic mobility on both starch and citrate agar media, solubility, mechanical precipitation rate of oxyhaemoglobins, and minimum gelling concentration, as well as by peptide mapping and amino-acid analysis of all beta-chain peptides. Taken together with the presence in Sicily of African blood group markers and certain historical considerations, it seems clear that the source of Hb S in Sicily is Africa. While the clinical severity in nine Sicilian children did not seem remarkably different from the disease in the USA, the most severe and fatal complications were not seen. Mean Hb F Was 10.5% and 2,3-diphosphoglycerate (2,3-DPG) values were higher in Sicilian homozygotes than in black USA counterparts (21.79 mumol/g Hb vs 15.16). Red cell AT values were also slightly higher in Sicilian patients. The presence of concomitant thalassaemia was excluded by both family studies and globin chain synthetic ratios. In conclusion, haemoglobin S in Sicilian homozygotes is identical to Hb S found in USA blacks. Although the severity of the disease seems quite similar in both groups of patients, other erythrocytic properties were found to be different. Whether these factors influence severity remains to be elucidated.

PMID: 7365760 [PubMed - indexed for MEDLINE]
 


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http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=3056831&dopt=Abstract
 

 
1: Hum Genet. 1988 Nov;80(3):207-18.
Characteristics of Mongoloid and neighboring populations based on the genetic markers of human immunoglobulins.

Matsumoto H. Department of Legal Medicine, Osaka Medical College, Japan.

Since the discovery in 1966 of the Gm ab3st gene, which characterizes Mongoloid populations, the distribution of allotypes of immunoglobulins (Gm) among Mongoloid populations scattered from Southeast Asia through East Asia to South America has been investigated, and the following conclusions can be drawn: 1. Mongoloid populations can be characterized by four Gm haplotypes, Gm ag, axg, ab3st, and afb1b3, and can be divided into two groups based on the analysis of genetic distances utilizing Gm haplotype frequency distributions: the first is a southern group characterized by a remarkably high frequency of Gm afb1b3 and a low frequency of Gm ag, and the second, a northern group characterized by a high frequency of both Gm ag and Gm ab3st but an extremely low frequency of Gm afb1b3. 2. Populations in China, mainly Han but including minority nationalities, show remarkable heterogeneity of Gm allotypes from north to south and contrast sharply to Korean and Japanese populations, which are considerably more homogenous with respect to these genetic markers. The center of dispersion of the Gm afb1b3 gene characterizing southern Mongoloids has been identified as the Guangxi and Yunnan area in the southwest of China. 3. The Gm ab3st gene, which is found with its the highest incidence among the northern Baikal Buriats, flows in all directions. However, this gene shows a precipitous drop from mainland China to Taiwan and Southeast Asia and from North to South America, although it is still found in high frequency among Eskimos, Koryaks, Yakuts, Tibetans, Olunchuns, Tungus, Koreans, Japanese, and Ainus. On the other hand, the gene was introduced into Huis, Uyghurs, Indians, Iranians, and spread as far as to include Hungarians and Sardinians in Italy. On the basis of these results, it is concluded that the Japanese race belongs to northern Mongoloids and that the origin of the Japanese race was in Siberia, and most likely in the Baikal area of the Soviet Union.

PMID: 3056831 [PubMed - indexed for MEDLINE]
 


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20% MIDDLE EASTERN HAPLOGROUP HG9 IN ITALY

According to a study conducted by Lluís Quintana-Murci et. al.. and published in The American Journal of Human Genetics, Volume 68, 2001, pages 537-542, the Middle Easter Haplogproup HG9 runs at 20% in Italy.

http://www.journals.uchicago.edu/AJHG/journal/issues/v68n2/002418/002418.html
 
 

American Journal of Human Genetics., 68:537-542, 2001
 
Y-Chromosome Lineages Trace Diffusion of People and Languages in Southwestern Asia
Lluís Quintana-Murci,1 Csilla Krausz,1 Tatiana Zerjal,2 S. Hamid Sayar,3 Michael F. Hammer,4 S. Qasim Mehdi,5 Qasim Ayub,5 Raheel Qamar,5 Aisha Mohyuddin,5 Uppala Radhakrishna,6 Mark A. Jobling,7 Chris Tyler-Smith,2 and Ken McElreavey1
. . .

HG 9, defined by the 12f2 deletion, is largely confined to caucasoid populations, with its highest frequencies being found in Middle Eastern populations.

In Iranian populations, HG 9 shows very high frequencies (30%60%). Populations from the southeastern Caspian region and the Zagros Mountains exhibit the highest frequencies so far observed (60%). High frequencies of HG 9 have been found throughout the Fertile Crescent region (Hammer et al. 2000): Palestinians, 51%; Lebanese, 46%; and Syrians, 57%. The incidences of HG 9 in Pakistan (18%) and northern India (19%) indicate a decreasing-frequency cline from Iran toward India.

Table 1
Frequency Distribution of HG 9 and HG 3 in Human Populations from Different Regions

REGIONa  N FREQUENCYb
(%) SOURCE
HG 9 HG 3
Iran:c
 
 
 
 
     Azarbaijan 83 34 17 Present study
     Zagros Mountains 34 59 6 Present study
     Western Caspian 32 53 3 Present study
     Eastern Caspian 25 56 20 Present study
     Tehran region 50 30 14 Present study
     Central-north 79 39 9 Present study
     Central-south 72 38 17 Present study
     Eastern provinces 26 35 31 Present study
Pakistan 708 18 32 Present study
India:
 
 
 
 
     Gujurat 58 19 26 Present study
     Jaunpur 152 NT 20 Zerjal et al. (1999)
     Indians mixed 72 NT 15 Hammer et al. (1998)
     Uttar Pradesh 62 7 NT Semino et al. (1996)
Sri Lanka 83 NT 15 Hammer et al. (1998)
Middle East:
 
 
 
 
     Lebanon 24 46 4 Hammer et al. (2000)
     Syria 91 57 9 Hammer et al. (2000)
     Palestine 73 51 0 Hammer et al. (2000)
Europe:
 
 
 
 
     Turkey 167 33 5 Rosser et al. (2000)
     Russia 122 4 47 Rosser et al. (2000)
     Ukraine 27 0 30 Rosser et al. (2000)
     Latvia 34 0 41 Rosser et al. (2000)
     Poland 112 4 54 Rosser et al. (2000)
     Greece 36 28 8 Rosser et al. (2000)
     Italy 99 20 2 Rosser et al. (2000)
     Spain 126 3 2 Rosser et al. (2000)
Africa:
 
 
 
 
     Algeria 27 41 0 Rosser et al. (2000)
     Sub-Saharan Africa 199 1 0 Hammer et al. (2000)
 

Offline BabylonianJew

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Re: Racial Admixture in various European Populations
« Reply #4 on: May 15, 2007, 01:08:58 PM »
Racial mixing in Spaniards: Annals of Human Genetics Volume 67 Issue 4 Page 312  - July 2003 
Joining the Pillars of Hercules: mtDNA Sequences Show Multidirectional Gene Flow in the Western Mediterranean
S. Plaza, F. Calafell, A. Helal, N. Bouzerna, G. Lefranc, J. Bertranpetit and D. Comas

Genetic Exchange Through the Mediterranean

Each of the subregions analysed (NW Africa and SW Europe) shows sequences that originated on the opposite shore of the Mediterranean. This is particularly clear in the case of U6 and L in SW Europe. L sequences are found at frequencies 3% in Iberia and 2.4% in Italy. Given the relatively high frequencies of L sequences in NW Africa, it is not clear whether they were contributed by the historical populations movements from the south to the north of the Mediterranean (such as the Moslem invasions of the 7th-11th centuries), or whether its presence is associated with other processes not directly linked to NW Africa. Out of 23 different L sequences in Iberia, two were also found in NW Africa (as well as in sub-Saharan Africa), and 7 others were found in sub-Saharan Africa (in a dataset comprising 1,158 individuals from 20 populations; Graven et al. 1995, Pinto et al. 1996; Watson et al. 1996; Mateu et al. 1997; Rando et al. 1998; Krings et al. 1999; Pereira et al. 2001; Brehm et al. 2002) but not in NW Africa. Treating the set of L sequences in Iberia as if it were a population reveals genetic distances from some W African populations, such as the Senegalese and Yoruba, that are slightly smaller than those between L sequences in Iberia and NW Africa. Thus, it may be the case that gene flow from NW Africa is not entirely responsible for the presence of L sequences in Iberia.

As hinted above, the presence of haplogroup U6 in Iberia may signal gene flow from NW Africa, and those of the subhaplogroup U6b1 recent gene flow from the Canary Islands. Haplogroup U6 is present at frequencies ranging from 0 to 7% in the various Iberian populations, with an average of 1.8%. Given that the frequency of U6 in NW Africa is 10%, the mtDNA contribution of NW Africa to Iberia can be estimated at 18%, with a 95% confidence interval of 8%-26% (estimated by sampling with replacement 10,000 times in populations having the same sample sizes and U6 frequencies as Iberia and NW Africa). This is larger than the contribution estimated with Y-chromosomal lineages (7%, 95% confidence interval 1%-14%, Bosch et al. 2001).

Full article can be found here.
 

 

http://www.journals.uchicago.edu/AJHG/journal/issues/v68n4/002582/002582.html
 The American Journal of Human Genetics, 68:1019-1029, 2001
High-Resolution Analysis of Human Y-Chromosome Variation Shows a Sharp Discontinuity and Limited Gene Flow between Northwestern Africa and the Iberian Peninsula
 

Elena Bosch, Francesc Calafell, David Comas, Peter J. Oefner, Peter A. Underhill, and Jaume Bertranpetit

 

In the present study we have analyzed 44 Y-chromosome biallelic polymorphisms in population samples from northwestern (NW) Africa and the Iberian Peninsula, which allowed us to place each chromosome unequivocally in a phylogenetic tree based on >150 polymorphisms. The most striking results are that contemporary NW African and Iberian populations were found to have originated from distinctly different patrilineages and that the Strait of Gibraltar seems to have acted as a strong (although not complete) barrier to gene flow. In NW African populations, an Upper Paleolithic colonization that probably had its origin in eastern Africa contributed 75% of the current gene pool. In comparison, 78% of contemporary Iberian Y chromosomes originated in an Upper Paleolithic expansion from western Asia, along the northern rim of the Mediterranean basin. Smaller contributions to these gene pools (constituting 13% of Y chromosomes in NW Africa and 10% of Y chromosomes in Iberia) came from the Middle East during the Neolithic and, during subsequent gene flow, from Sub-Saharan to NW Africa. Finally, bidirectional gene flow across the Strait of Gibraltar has been detected: the genetic contribution of European Y chromosomes to the NW African gene pool is estimated at 4%, and NW African populations may have contributed 7% of Iberian Y chromosomes. The Islamic rule of Spain, which began in A.D. 711 and lasted almost 8 centuries, left only a minor contribution to the current Iberian Y-chromosome pool. The high-resolution analysis of the Y chromosome allows us to separate successive migratory components and to precisely quantify each historical layer.
 

 


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MOORISH INFLUENCE IN IBERIA

According to the study Human Y-Chromosome variation in the Western Mediterranean area: implications for the peopling of the region. by R Scozzari, et. al., and published in Human Immunology, 62(9):871-874 (2001)., the newly defined haplogroup 25.2 reveals the influence of the Moors in Iberia:

http://www.elsevier.com/gej-ng/10/21/30/47/39/28/article.pdf (requires subscription to access)
 
       Human Immunology, 62(9):871-874 (2001)
 
Human Y-Chromosome variation in the Western Mediterranean area: implications for the peopling of the region.

by R Scozzari, F Cruciani, A Pangracio, P Santolamazza, G Vona, P Moral, V Latini, L Varesi, M Memmi, V Romano, G De Leo, M Gennarelli, J Jaruzellska, R Villems, J Parik, V Macaulay, A Torroni.

"Among the Spanish populations, a small sample of 19 subjects from an isolated population living in a restricted area (Pas valleys) of the community of Cantabria is of particular interest. The origin of this population is not clearly defined [11], although some historical information traces the peopling of the region back to the 11th century as a result of a repopulating from different sources, including Moorish slaves [12].

The newly defined HG25.2 originated on a HG25.1 background. In Africa, HG25.2 is observed in 29% Arabs and 71% of Berbers from Morocco, but is not found in those Ethiopian populations in which a high frequency of the ancestral HG25.1 is observed (R.Scozzari and associates, unpublished results [18]).

Outside Northern Africa, HG25.2 was seen at generally low frequencies in Spain, France, and Italy, although no traces could be detected in the Near East.

However, particularly high frequency of this haplogroup (42%) was found in the Pasiego of the Pas valleys. In the  correspondence analysis (Figure 6), the Pasiego do not cluster with the other Spanish populations, but rather with the Arabs and Berbers from Morocco, supporting historic and demographic records that would trace back the origin this population to a heterogeneous resettlement, including also Moslem slaves [12].

The microsatellite diversity associated with HG25.2 provided coalescence age estimates of ;1400 YBP (CI 5 540–2200 YBP). Although it is not possible at present to determine where HG25.2 originated, the simplest interpretation of our data is that HG25.2 diverged from the ancestor HG25.1 somewhere in North Africa a few thousand years ago. A founder effect led first to its expansion among the Berber populations, followed, in historical time, by its spread into the Iberian peninsula.

Interestingly, the distribution YAP(1)/DYS271(A) chromosomes was recently demonstrated to be strongly clinal in Portugal, with the highest frequencies in the south, and interpreted as a reflection the Moorish invasions from North Africa in the Middle Ages [45]. A dissection of the Portuguese YAP(1)/ DYS271(A) chromosomes by PN2 and XY275Y would determine whether they indeed belong to HG25.2, could be inferred from an early report, which unfortunately did not provide haplotype information [46]."
 

HG25.2, which most likely indicates recent North African admixture, was found at the following frequencies in this study:

Southern Spaniard: 1.6
Asturias: 2.2
Pasiegos: 42.1
Morrocan Arab: 28.6
Morrocan Berber: 71


Offline BabylonianJew

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Re: Racial Admixture in various European Populations
« Reply #5 on: May 15, 2007, 01:10:22 PM »
Racial admixture in Portugesse, Berbers,Negroes, and Arabs influence: Diversity of mtDNA lineages in Portugal: not a genetic edge of European variation.
Annals of Human Genetics 64 (6), 491-506.

These haplogroups have been reported to be characteristic of African populations, where their frequency is inversely correlated with the North-South axis: the frequency of U6 is high in North Africa and decreases in a southerly direction, being almost absent south of the equator; the L cluster has an opposite distribution (Rando et al. 1998, 1999; Watson et al. 1996; Mateu et al. 1996).

In Portugal, as well as generally in Iberia, many migration waves from both North and sub-Saharan African populations are well documented. The geographical proximity of North Africa and the Iberian Peninsula certainly afforded many opportunities for mutual population contacts. Among them, we stress the movement of Berbers and Arabs that took place during the very recent Muslim rule of Iberia (from the 8th century to the end of the 15th, in some regions). In addition, many sub-Saharan individuals entered the region during the slave trade period, from its very beginning (middle 15th century) until its total ban in the late 19th century.

As it would be interesting to find out the origin of the L and U6 sequences detected in Portugal, we have tried to compare the motifs of the sequences observed in Portugal with those described in the literature for several populations (Figures 3 and 4). However most of the matches found for the Portuguese sequences were with sequences widely distributed in Africa, and no clear pattern of geographic clustering was detected.

A striking aspect observed for the U6 haplogroup was that 5 out of 7 of the Portuguese sequences were unique to Portugal, not allowing, therefore, any accurate assignment of their geographical origin. The Canarian characteristic sub-haplogroup U6b1 (Rando et al. 1999), observed in other Iberian samples, was not detected in the present study.

Admitting that U6 sequences could have been at least partially introduced by Berber people during the Muslim rule of Iberia, it is strange to find them restricted to North Portugal. As a matter of fact, most historical sources document a deeper influence of Berber (as well as Arab) people in Central and particularly South Iberia (as judged from toponyms and general cultural aænities), compared to North Iberia where the Muslim presence is recorded to have been more ephemeral and consequently to have made less cultural and demographic impact. The data does not exclude the possibility that U6 introductions could have been additionally reinforced by later sub-Saharan inputs mediated by the African slave trade. Even if this mixed scenario is plausible, the presence of U6 sequences exclusively in North Portugal is a question that deserves further analysis. The hypothesis of an earlier introduction in the region does not seem to be favoured, neither by its presence in a restricted geographical area, nor by the high level of heterogeneity that characterises the set of sequences that were found among this haplogroup.



With respect to the L sequences, it is widely accepted that they have a sub-Saharan origin, excepting some L3* lineages that, as analysis of Figure 4 suggests, might indeed have a non-African origin. The presence of L sequences in North African regions does not allow us to exclude the possibility that population influxes from this region, namely the above referred Berber/Arab movement, have introduced significant fraction of L sequences into Iberia. However, it seems more likely that most of the L lineages found nowadays in Portugal have been carried by African slaves, since the country was actively involved in the Transatlantic slave trade. Nine out of 17 L sequences found in this study showed matches with widespread African sequences, and with regard to the 8 remaining sequences the absence of matches can be due to the present bias in the description of sub-Saharan mtDNA variability. Broad areas corresponding to Ivory Coast, Angola and Mozambique, which represented very important sources of African slaves, remain uncharacterised.

There were more African slaves in Portugal than in any other European country: in 1550, Lisbon boasted 10000 resident slaves in a population of 100000, and Portugal as a whole probably had over 40000 (Thomas, 1998). In the mid-sixteenth century the birth of slaves' children was stimulated in Portugal for internal trade purposes. Inter-breeding between autochthonous individuals and African slaves certainly occurred and the predominant mating must have been between slave African females and autochthonous males, due to social pressures and also for legal reasons: offspring of slave females would be slaves, whereas offspring of slave males would not. Therefore, breeding between slave African males and white females, besides being socially repressed, would not bring any economic profit.

If the pattern of genetic admixture was markedly sex influenced, the signature of this recent African influence would be expected to be very different in the maternally inherited gene pool and in the paternally inherited one. In a recent study based on Y chromosome biallelic markers (Pereira et al. 2000) we have reported the absence of typical sub-Saharan haplogroups in the Y chromosome Portuguese pool. This finding, and the detection of L sequences at 7.1% in the mitochondrial pool, both seem to support the above-mentioned pattern of admixture with African slaves.

Sharing the features of mtDNA diversity generally registered in Europeans (all European haplogroups were detected), Portugal has in addition received significant North and sub-Saharan African influences. Frequencies of haplogroups specific to these regions were higher than those reported for other European populations: 7% of North African sequences were detected (restricted to North Portugal and representing almost 3%of the total sample), and sub-Saharan African sequences were found to be spread throughout the country, with frequencies between 5% and 9.8%. Although statistically significant differences were not detected between the three sub-samples considered, the geographic distribution pattern observed for U6 and L sequences strongly suggest that different population movements were responsible for their introduction into the country, although none of them had enough demographic impact to induce regional differentiation.

The introduction of L sequences in Portugal was tentatively imputed mainly to the modern slave trade that occurred between the 15th and 19th centuries. Both the great number of slaves that entered Portugal and their very diverse African geographic origin are consistent with the data set now reported. However, we cannot exclude some North-African contribution to present-day Portuguese L lineages.

While the population movement associated with the slave trade may be responsible by some U6 inputs, we suggest that U6 sequences were predominantly introduced into Portugal during the Berber/Arab invasion of the Peninsula. However, the observation that haplogroup U6 is restricted to North Portugal is puzzling, considering the more pronounced impact of the Muslin rule in south Iberia and the widespread presence of African slaves throughout the country, and deserves further investigation.

Full PDF can be accessed here.
 


--------------------------------------------------------------------------------

A recent study has suggested that at least some of these African lineages detected in the Pereira study above, could be Neolithic in origin, as detailed in a report by Gonzalez. et. al, titled 'Mitochondrial DNA affinities at the Atlantic Fringe of Europe' and published in the  American Journal of Physical Anthropology  2003 Apr;120(4):391-404:

http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=12627534&dopt=Abstract

 
Mitochondrial DNA affinities at the Atlantic fringe of Europe.

Gonzalez AM, Brehm A, Perez JA, Maca-Meyer N, Flores C, Cabrera VM.

Departamento de Genetica, Universidad de La Laguna, 38271 La Laguna, Tenerife, Spain. [email protected]

Mitochondrial DNA analysis of Atlantic European samples has detected significant latitudinal clines for several clusters with Paleolithic (H) and Neolithic (J, U4, U5a1, and U5a1a) coalescence ages in Europe. These gradients may be explained as the result of Neolithic influence on a rather homogeneous Paleolithic background. There is also evidence that some Neolithic clusters reached this border by a continental route (J, J1, J1a, U5a1, and U5a1a), whereas others (J2) did so through the Mediterranean coast. An important gene flow from Africa was detected in the Atlantic Iberia. Specific sub-Saharan lineages appeared mainly restricted to southern Portugal, and could be attributed to historic Black slave trade in the area and to a probable Saharan Neolithic influence. In fact, U6 haplotypes of specific North African origin have only been detected in the Iberian peninsula northwards from central Portugal. Based on this peculiar distribution and the high diversity pi value (0.014 +/- 0.001) in this area compared to North Africa (0.006 +/- 0.001), we reject the proposal that only historic events such as the Moslem occupation are the main cause of this gene flow, and instead propose a pre-Neolithic origin for it.

The haplogroup frequencies and sample sizes for the populations analyzed are given in Table 1. The haplotype with the reference sequence (CRS, Anderson et al., 1981) is the most abundant haplotype in all samples, although values range from 11.7% in northwest Africa to 21.7% in north Portugal.

As expected, sub-Saharan African influence, represented by baplotypes classified in L and Ml clusters, is important in northwest Africa (26.1%) but negligible in Europe, with the exception of south Portugal (11.7%).

On the other hand, subhaplogroup U6, of North African origin (Rando et al., 1998), has a local presence in Europe, being detected only in northwest lberian Peninsula. The differential geographic distributions of these sub-Saharan African and northwest African haplogroups in the Iberian Peninsula are statistically significant: L and Ml clusters are more abundant in south Portugal (x = 9.81; P < 0.01), and U6 in northern areas (x = 5.83; P < 0.05).

Cluster U5, with coalescence ages in the early Upper Paleolithic, and a probable European origin (Richards et a!, 2000) reaches its highest frequencies for its ancestral motives in Britain (x = 11.74; P < 0.001) when compared to other continental areas such as Scandinavia, Germany, France, and the Iberian Peninsula.

With respect to northwest Africa, the geographically localized distribution of matches and haplotypes of sub-Saharan  African and northwest African origin in the Iberian  Peninsula is noteworthy.  This distribution cannot be totally explained by  a historic genetic influence  from the Moslem occupation (Pereira et. al., 2000). During  that time, the haplotype composition of northwest  Africa had to be similar to that of the present,  and for this reason, sub-Saharan African L and northwest African  U6 haplotypes should be uniformly  distributed in the Iberian peninsula.

However, with respect to the sub-Saharan Africa lineages, the recent history of the Black slave trade carried out by the Portuguese (mainly in the 15th and 16th centuries), with a well-documented import in southern Portugal (Godinho, 1983), could also be a plausible alternative to explain the presence of these African haplotypes in this region. (Pereira et al 2000) To test this possibility we compared the proportion of sub-Saharan Africa haplotype matches between the Iberian Peninsula and northwest Africa (0.75%) with those of the Iberian Peninsula and a sample of sub-Saharan Africans from the Gulf of Guinea.

These results suggest that, although both prehistoric and historical influences likely contributed to the sub-Saharan African haplotype pool present in the Iberian peninsula, the former seems to be more important.

Our results are in agreement with the gene flow (19.5%) from northwest Africa to the Iberian Peninsula estimated in a recent study of variation in the autosomic CD4 locus (Flores et al., 2000b), and with the evidence of northwest African African male input in Iberia calculated at around 20%, using the relative frequency of northwest African Y-chromosome-specific markers in Iberian samples (Flores et al, 2000a).

Furthermore, our results clearly reinforce, extend, and clarify the preliminary clues of an important mtDNA contribution from northwest Africa into the Iberian Peninsula (Côrte-Real et al., 1996; Rando et al., 1998; Flores et al., 2000a; Rocha et al., 1999). On the basis of the Lib frequencies detected in Spanish and Portuguese samples (2—3%) and those found in western Africa (10-30%), a significant influence (at least 10%) of North Africans in have reached the Iberian Peninsula gene pool has also been admitted (Rocha  et al., 1999).

In a similar way, and discarding possible genetic drift effects, our own data allow us to make minimal estimates of the maternal African pre Neolithic, and/or recent slave trade input into Iberia.  For the former, we consider only the mean value of the U6 frequency in northern African populations, excluding Saharans, Tuareg, and Mauritanians (16%), as the pre-Neolithic frequency in that area, and the present frequency in the whole Iberian Peninsula (2.3%) as the result of the northwest African gene flow at that time.

The value obtained (14%) could be as high as 35% using the data of Côrte-Real et al. (1996), or 27% with our north Portugal sample.

In the same vein, the Saharan Neolithic gene flow can be estimated as 13%, taking the actual frequencies for the sub-Saharan African haplogroups (51%) in southern northwest African samples (Tuareg, Saharans, and Mauritanians) as the frequency of the African Neolithic, and that of the Iberian Peninsula (6.8%) as the result of the putative Neolithic maternal gene flow. This value could rise to 23% when only south Portugal is taken into account.

However, if we admit a recent 10% of slave trade input into this region, as historically documented (Godinho, 1983), 13% would be left for the putative Saharan Neolithic gene flow.

Full PDF copy of this article available here.
 


--------------------------------------------------------------------------------

MOORISH INFLUENCE IN IBERIA

According to the study Human Y-Chromosome variation in the Western Mediterranean area: implications for the peopling of the region. by R Scozzari, et. al., and published in Human Immunology, 62(9):871-874 (2001)., the newly defined haplogroup 25.2 reveals the influence of the Moors in Iberia:

http://www.elsevier.com/gej-ng/10/21/30/47/39/28/article.pdf (requires subscription to access)
 
       Human Immunology, 62(9):871-874 (2001)
 
Human Y-Chromosome variation in the Western Mediterranean area: implications for the peopling of the region.

by R Scozzari, F Cruciani, A Pangracio, P Santolamazza, G Vona, P Moral, V Latini, L Varesi, M Memmi, V Romano, G De Leo, M Gennarelli, J Jaruzellska, R Villems, J Parik, V Macaulay, A Torroni.

"Among the Spanish populations, a small sample of 19 subjects from an isolated population living in a restricted area (Pas valleys) of the community of Cantabria is of particular interest. The origin of this population is not clearly defined [11], although some historical information traces the peopling of the region back to the 11th century as a result of a repopulating from different sources, including Moorish slaves [12].

The newly defined HG25.2 originated on a HG25.1 background. In Africa, HG25.2 is observed in 29% Arabs and 71% of Berbers from Morocco, but is not found in those Ethiopian populations in which a high frequency of the ancestral HG25.1 is observed (R.Scozzari and associates, unpublished results [18]).

Outside Northern Africa, HG25.2 was seen at generally low frequencies in Spain, France, and Italy, although no traces could be detected in the Near East.

However, particularly high frequency of this haplogroup (42%) was found in the Pasiego of the Pas valleys. In the  correspondence analysis (Figure 6), the Pasiego do not cluster with the other Spanish populations, but rather with the Arabs and Berbers from Morocco, supporting historic and demographic records that would trace back the origin this population to a heterogeneous resettlement, including also Moslem slaves [12].

The microsatellite diversity associated with HG25.2 provided coalescence age estimates of ;1400 YBP (CI 5 540–2200 YBP). Although it is not possible at present to determine where HG25.2 originated, the simplest interpretation of our data is that HG25.2 diverged from the ancestor HG25.1 somewhere in North Africa a few thousand years ago. A founder effect led first to its expansion among the Berber populations, followed, in historical time, by its spread into the Iberian peninsula.

Interestingly, the distribution YAP(1)/DYS271(A) chromosomes was recently demonstrated to be strongly clinal in Portugal, with the highest frequencies in the south, and interpreted as a reflection the Moorish invasions from North Africa in the Middle Ages [45]. A dissection of the Portuguese YAP(1)/ DYS271(A) chromosomes by PN2 and XY275Y would determine whether they indeed belong to HG25.2, could be inferred from an early report, which unfortunately did not provide haplotype information [46]."
 

HG25.2, which most likely indicates recent North African admixture, was found at the following frequencies in this study:

Southern Spaniard: 1.6
Asturias: 2.2
Pasiegos: 42.1
Morrocan Arab: 28.6
Morrocan Berber: 71

Presuming that

(1) the mixed race North African Moors had between 28.6% and 71% HG25.2;

(2) there was no HG25.2 in Iberia prior to the Moorish invasion; and

(3) the average level of HG25.2 across Iberia today is 2%;

This would imply that about 3-7% of Iberian male lineages are of Moorish origin, though this is evidently higher in places like the Pas valley.


--------------------------------------------------------------------------------

Offline BabylonianJew

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Re: Racial Admixture in various European Populations
« Reply #6 on: May 15, 2007, 01:12:56 PM »
Racial admixture in Northern Europeans Mongol strain:has been known for a long time that the Sámi, or Lapp, people of Northern Scandinavia are of Northern Asiatic origin, and that they have mixed heavily with Nordic elements to produce a wide variety of physical types, all of whom claim to be Sámi. This has been further complicated by the Sámi's own definition of their group as 'anyone with one Sámi ancestor" leading to a large number of what would otherwise be indistinguishable Nordic types claiming to be members of the Sámi tribe.

In chapter 24 of this book, mention was made of this Sámi group, along with some illustrations. Here are some more examples of Sámi:


 
 
 
Above: Sámi physical types vary from (left) overtly Nordic; slightly Mongoloid (center) and overtly Mongoloid (right).
 

 


 
Above: A meeting of the Sámi parliament in Finland appears to be dominated by Nordic looking types.
 

The Sámi are however small in number: it is estimated that currently there are only about 75,000 Sámi in all, spread over Norway, Sweden, Finland and Russia.

  Total Population No. of Sámi
Norway 4,534,996 40,000
Sweden 8,924,000 15-25,000
Finland 5,185,492 6,500
Russia 143,671,873 2,000

(Population statistics from The Online Population Index Counter, US Census Bureau, http://www.anthro.mankato.msus.edu/information/population/ 

and "The Sámi in Finland"  http://virtual.finland.fi/finfo/english/saameng.html)

It is thus clear that Finland has the lowest number of Sámi of the Scandinavian countries. Yet it is precisely Finland where it is claimed that the largest amount of Northern Asiatic genetic input has been.

This Northern Asiatic genetic input has been estimated to be as high as 55 percent in Finland, 8 percent in Norway, and 55 percent in Latvia and Lithuania. These estimates are based on the existence of a genetic marker, 'Tat-C' or 'Haplogroup N3', which, it is claimed, originated amongst Asiatic tribes in Siberia.

GENETIC ARGUMENTS IN FAVOR OF 'ASIATIC' ORIGIN OF TAT-C

Despite the latest research (see below) strongly suggesting that the "Tat-C" marker is actually a Paleolithic trace marker from an original Ice-Age population of North Eastern Europe, and not an exclusively Northern Asiatic trait, it is still worthwhile to overview the the presumption that Tat-C is an Asiatic marker.

So for example, in a report prepared titled Dual Origins of Finns Revealed by Y Chromosome Haplotype Variation by Rick Kittles et. al. and published in the American Journal of Human Genetics, Volume 62, pages 1171-1179, in 1998, it is asserted that Finns have a dual origin: European and Asian:

http://www.journals.uchicago.edu/AJHG/journal/issues/v62n5/970788/970788.text.html
 
American Journal of Human Genetics, 62:1171-1179, 1998
0002-9297/98/6205-0023
Dual Origins of Finns Revealed by Y Chromosome Haplotype Variation
Rick A. Kittles, Markus Perola, Leena Peltonen, Andrew W. Bergen, Richard A. Aragon, Matti Virkkunen, Markku Linnoila, David Goldman, and Jeffrey C. Long
Received December 5, 1997; accepted for publication March 13, 1998; electronically published April 17, 1998.

Summary

Thus, mixed or dual origins for the Finns have been proposed. Here we present genetic evidence for the dual origins of Finns by evaluating the pattern of Y chromosome variation in 280 unrelated males from nine Finnish provinces.

The geographic distribution and time of expansion for the two common Y haplotypes correlate well with archeological evidence for two culturally and geographically distinct groups of settlers. Also, a northeastern to southwestern gradient of Y haplotype frequencies provides convincing evidence for recent male migration from rural areas into urban Finland.

Compound haplotypes were constructed by use of seven Y-specific microsatellite loci, a restriction site at the Y alphoid satellite DYZ3 locus (Santos et al. 1995), and a deletion polymorphism at the DYF155S2 locus (Jobling et al. 1996) for 280 unrelated males from nine Finnish provinces. The deletion polymorphism is common in populations with Asian ancestry and has been observed in Finland at a frequency of 55% (Jobling et al. 1996). Y chromosome compound haplotypes constructed by use of these Y-specific loci are extremely informative for population genetic studies, mainly because of the high mutation rates of microsatellite loci, their paternal/clonal inheritance, and an effective population size, 25% that of autosomes. Here we present genetic evidence in support of two independent groups of settlers founding Finland, one from Asia and the other from Europe.

Three distinct haplogroups were observed. Haplogroup A is the largest (55%), and all members of this group of haplotypes share the DYF155S2 deletion polymorphism associated with several Asian populations (Jobling et al. 1996). Haplogroups B and C do not possess the deletion, but are defined by the presence or absence of the HindIII restriction site at the DYZ3 locus. Haplogroup B, the second largest group of haplotypes (29%), possesses the restriction site. Haplogroup B is phylogenetically complex and is composed of four subgroups. All four subgroups are found in other European populations (unpublished data).



Figure 2 (above) depicts the geographic distribution of haplotypes A/49 and B/69. Interestingly, haplotype A/49 was found in highest frequency in the eastern provinces of Northern Karelia, Kuopio, and Kymi. The most striking of these provinces is Northern Karelia, where 50% of males possess haplotype A/49, whereas only 2% possess haplotype B/69. The opposite pattern is observed in the southwest.

Haplotype A/49 is restricted to Finland and has not been found in other Scandinavian populations (unpublished data). The other common Y haplotype (B/69) lacks the deletion polymorphism and is observed in other European populations. From the geographical distribution and molecular divergence of haplotypes A/49 and B/69, we conclude that they represent two major founding Y chromosome lineages in Finland.

Our results argue against the single-origin model. Specifically, we find evidence that the initial group of settlers provided a substantial contribution (55%) to the present Finnish Y chromosome gene pool. These settlers were of Asian ancestry and were followed by a second, genetically distinct wave of settlers. This second group, possessing haplogroup B, may have arrived in Finland with the wave of agriculturists who shaped much of the genetic landscape of Europe (Sajantila and Paabo 1995). These estimates are consistent with archeological data that suggest that the first settlers were Uralic speakers who arrived 4,000 years ago (Fodor and Czeizel 1991) and that a later group settled along the southern shores 2,000 years ago (Luho 1976).

Full article at: http://www.journals.uchicago.edu/AJHG/journal/issues/v62n5/970788/970788.text.html
 

 

A study by Jeffrey Lell et, al, titled The Dual Origin and Siberian Affinities of Native American Y Chromosomes, published in the American Journal, of Human Genetics, volume 70, pages 192-206, in 2002, asserted that the 'Tat-C' marker was 'Siberian' in origin:

 

http://www.journals.uchicago.edu/AJHG/journal/issues/v70n1/013099/013099.text.html
 
Am. J. Hum. Genet., 70:192-206, 2002,
The American Society of Human Genetics.
 
 
The Dual Origin and Siberian Affinities of Native American Y Chromosomes '

Jeffrey T. Lell, et. al.

The Tat-C haplogroup was observed at significant frequencies in each of the southern Middle Siberian populations studied. Surprisingly, it reached its highest frequency in the Siberian Eskimos and Chukchi from the Chukotkan peninsula. The Tat-C haplogroup was absent in the Lower Amur and Sea of Okhotsk region populations that have maintained greater geographic and/or linguistic isolation (e.g., the Udegeys, Nivkhs, and Upriver Negidals) and was only detected in the populations likely to have had recent contact or shared origins with the populations of southern Middle Siberia (e.g., the Okhotsk Evenks, Ulchi/Nanai, and Downriver Negidals). Because the Tat-C polymorphism originated on a Y chromosome containing the DYS7C deletion (haplogroup 7C), which was present only in the Middle Siberian Tuvans, Buryats, Tofalars, and Yenisey Evenks, the Tat-C haplogroup probably entered the Lower Amur and eastern Siberia from southern Middle Siberia. This conclusion is consistent with the previous hypothesis that the Tat-C and 7C haplogroups arose in central Asia and migrated west to northern Europe and east to Chukotka (Zerjal et al. 1997).
 

On this basis, the assumption has been made that around 55% of Finnish Y Chromosomes, 47% of Lithuanian Y Chromosomes, 32% of Latvian Y-Chromosomes, 37% of Lithuanian Y-Chromosomes, and 5.7% of Norwegian Y-Chromosomes are 'Asiatic' in origin.

As Y-Chromosomes make up, in theory, just under half of an individuals' DNA (the other two components being autosomal DNA, inherited from both parents and mtDNA, inherited only from the maternal line), this would imply that  up to 27 percent  of Finns, 24% of Lithuanians, 16% of Latvians and 2.6% of Norwegians could be of mixed ancestry.

This assertion has been given credence by the existence of some obviously mixed Nordic-Asiatic types which do exist in North Eastern Europe: for example, these two specimens from Sweden and Russia:


 
 
Illustrations from HFK Günther's "Racial Elements of European History", Methuen & Co. 1927
 


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LATEST RESEARCH REJECTS ASIATIC ORIGIN OF TAT-C

However, the situation is not as simple as might seem. In reality, recent research indicates that the 'Tat-C' marker could well have been an original Caucasian Paleolithic marker of a Ice Age or Pre-Ice Age population, which spread west, and not east.

The foremost proponent of this belief is the Estonian professor of evolutionary biology Richard Villems, who explained the origin of Tat-C in an article titled "The Finno-Ugric connection, genetics-wise, could be bigger than imagined", published in the Helsingin Sanomat, International Edition, Tuesday 30.1.2001 ):

http://www.helsinki-hs.net/news.asp?id=20010130IE4
 

 
The Finno-Ugric connection, genetics-wise, could be bigger than imagined
 

Even the Balts are relatives, despite their language

By Jukka Rislakki in Tallinn

The latest genetics research indicates that we Finns have a great many "relatives" out there in Eastern Europe and Siberia, and that these peoples share a common ancestor who was apparently Finno-Ugric in origin. At the same time, it would seem that the Estonians are genetically closer to their Latvian neighbours than they are to their linguistic relatives the Finns.

All the "ancient East Europeans" - the group does not include the Slavic tribes, who only turned up around 1400 years ago - have a 40 to 50% incidence of a common paternal genetic inheritance, in other words a unique male Y-chromosome polymorph, according to the Estonian academician and professor of evolutionary biology Richard Villems.

The ancient East European races in this context refers to the Balts, the Finns, the Sámi peoples of Lapland, and other races related to the Finno-Ugric stock.

Man emerged originally from Africa, but it is possible that the "Adam" of East European man, or at least one of the Adams, was a Finno-Ugrian, says Villems. In addition to his duties at the University of Tartu, the 56-year-old Villems is Director of the Estonian Biocentre.

"Although the Balts (the Latvians and Lithuanians) each speak an Indo-European language, unlike us Finno-Ugrians, they exhibit this chromosome pattern roughly as often as do the Finns, the Karelians, the Estonians, the Sámi, and other Finno-Ugrian groups", Villems argues.

In this respect the Balts differ from other Indo-Europeans, whether they may speak Slavic, Germanic, or Romance languages.

The remainder of the paternal line comes from the West. On the maternal side, our genetic history ties us inextricably with the Western Europeans. Estonians have only 0.5% Mongol lineage and the Finns around 1%, with the Sámi showing a slightly larger incidence.

The peculiar Y chromosomal DNA variant, known as Tat C, is also dominant in almost all the indigenous peoples of Siberia, from the nomadic Yakuts right across to the Chukchis and Siberian Inuits living on the shores of the Bering Strait - regardless of what language they may communicate in.

According to Prof. Villems, the "point" in all this is that among the Finno-Ugric races of Europe this genetic inheritance is much more diverse, more multibranched, and hence apparently older than among any of the Siberian peoples.

It is characteristic of the European Finno-Ugrians both in the area of the Baltic Sea and in the Volga region (the ethnic Maris living in the Mari Republic east of Nizhni-Novgorod and west of the Urals). "It is an original Finn-Ugric feature. We have observance of between 35 and 60%, or about half of the paternal inheritance, and it has penetrated to some extent into Norway and rather less to Sweden."

The figures for Poles, Slovaks, and Hungarians are already very very small, however, and in Western and Mediterranean Europe they go right down to zero."

Researchers at Oxford also spotted the spread of this "Northern Gene" three years ago. Villems shrugs his shoulders, "But they simply accepted the old theory: they believed it confirmed the idea that the Finno-Ugric tribes originated from Siberia."

Villems asserts that the contrary is true, however: the movement was one from west to east and not westwards from Siberia. He argues that the genetic variant could have been transported for instance by warriors. "And at the same time they could possibly have carried the proto Finno-Ugric language with them".

The same gene morphism has been found from the Inuits of Greenland. On seeing how this mutation has spread right the way across the northern parts of the Northern Hemisphere and nowhere else, the professor has started to wonder if we might be dealing with a gene that somehow helps us to acclimatise ourselves - to withstand extreme cold.

He also believes that our Finno-Ugrian ancestors might well have been living here a good while before the last Ice Age (around 20,000 years ago). "They could perhaps have arrived even at the same sort of time as the first great wave of migration as man spread into Europe some 40,000 years ago."

There were people living the whole time along the southern fringes of the continental ice mass. When the ice sheets were was at their most extensive, the Finno-Ugric tribe would have lived for some time down in the region between the Don and Dniester rivers, in what is now part of the Ukraine. Radio carbon dating studies show that this area was more densely settled during the Ice Age than it was either before or afterwards.

Professor Villems sides with those scholars of linguistics who claim that the original Finno-Ugric tongue was spoken widely through Northern Europe - in Fenno-Scandia and the Baltic region all the way down to the German coast. "This fits the picture very well."

Languages change immeasurably more quickly than do features of genetic inheritance. Villems regards it as a given that our common genetic identity emerged well before the Indo-European language that is spoken by the Latvians and the Lithuanians.

More advanced grain cultivating cultures and the Indo-European language strain gradually penetrated into the north. They never made it up to the coldest areas. The language boundary remained where it is today: between Estonia and Latvia.

But the gene frontier would have none of this. "One could say that the Estonians are genetically a shade closer to the Karelians and to the Latvians - at least to the northern Latvians - than they are to the Finns, from whom they are divided by the Gulf of Finland. In this way the Estonians also have a tad more of the Central European about them."

Amongst the Latvians one can of course also see the influence of the Livonian Knights (the crusading order that conquered and converted this area in the 13th century). But what is perhaps most bizarre of all is that even the Lithuanians have much the same frequency of occurrence of that Y chromosome as do the Estonians and the Finns.

"Just across the border in Poland, however, it disappears abruptly. There's a very striking genetic frontier there, in spite of the fact that the two nations are neighbours with nothing much in the way of rivers or mountain ranges to prevent access either way, and they have even lived under the same rulers for centuries!"

The same paradox exists to the south-east: the Balts and the Belarussians have a similar genetic wall between them, and the frequency of the Y chromosome mutation in Belarus is very low.

"This sort of thing gets one thinking about how people behaved. Apparently the societies were very clearly separated. I mean, the gene would have travelled in a flash if the soldiers from one group had raped the women of another, for instance."

Helsingin Sanomat / First published in print 24.1.2001
 

Note the research which Professor Villems quotes which states that Finns have "less than one percent" Mongol ancestry.

The Russian Journal of Genetics (http://www.maik.rssi.ru/cgi-bin/journal.pl?name=geneng&page=main) Editor in Chief, Georgii P. Georgiev, Institute of Gene Biology, Moscow, Russia, in its March 2003 edition, observed that no definite conclusion could be made as to the racial origin of Tat-C, and confirmed that it could well be a Caucasoid marker spread amongst several racial groupings:

http://www.maik.rssi.ru/cgi-bin/search.pl?type=abstract&name=geneng&number=3&year=2&page=309
 
  Russian Journal of Genetics 38(3): 309-314; Mar 2002
 
Polymorphism of the Y-Chromosome Diallelic Loci
in Ethnic Groups of the AltaiSayan Region
M. V. Derenko, B. A. Malyarchuk, G. A. Denisova, Ch. M. Dorzhu, O. N. Karamchakova, F. A. Luzina, E. A. Lotosh, I. K. Dambueva, U. N. Ondar, and I. A. Zakharov

Received April 10, 2001

Abstract—Using the data on five diallellic Y-chromosome loci (DYS199, 92R7, SRY1532, RBF5, and DYS287) polymorphism, genetic structures of the five Turkic-speaking ethnic groups of the Altai–Sayan upland (Tuvin-ians, Sojots, Shorians, Khakassians, and Southern Altaians (Altai-Kizhi), were described. The gene pools of the populations examined were characterized by the presence of pronounced paleo-Caucasoid component (92R7-T-lineages). The frequency of this component increased westward, reaching more than 70% in Shorians and Southern Altaians. Haplotype TAT-C (RBF5 locus) was observed

Ethnic groups of the Altai-Sayan region are different in respect of their anthropological features, though they share the prevalence of Turkic language and culture in their genesis. The formation of the indigenous anthropological type of the Altai-Sayan upland is traced back to the Neolithic and characterized by intense admixture of the European and Mongoloid groups. In most indigenous people of the region, namely, Southern Altaians, Tuvinians from the steppe regions, and some groups of Khakassians, the most Mongoloid, Central Asian type prevails. This type is a complex racial genetic structure, the origin of which traces back to the Mongoloid groups that underwent admixture at different periods of time (from the ancient times to the late Middle Ages). In respect of their anthropologic features, Shorians along with some Ugric and Samoyed peoples are typical representatives of the Uralic race. The features of the Uralic race, occupying intermediate position between large Mongoloid and Caucasoid races, can be also observed among Northern Altaians and some of the Khakassian groups [1-3].



Haplotype 3, defined by the TAT-C allele and found in 14.6% of Tuvinians, 5.4% of Altaians, 11.8% of Sojots, and 18.8% of Khakassians, cannot be  unambiguously attributed to either Mongoloid or Caucasoid lineages. It is established that TAT-C allele of the RBF5 locus is distributed predominantly in Northern Eurasia.

Maximum frequencies of this allele were observed in Yakuts (86%), Buryats from Mongolia (52%), and also in such Finno-Ugric peoples as Finns (61%), Estonians (37%), and Maris (33%) [12, 17]. The TAT-C allele was also found in populations of the Volga-Ural region with the frequencies varying from 9% in Mordovians to 68% in Udmurts [26]. Zerial et al. suggested that this mutation first arose in the populations of Asia and then dispersed over the territory of Northern Europe reaching Finland, which can indicate substantial genetic contribution of Mongoloids to the development of Northern European peoples [17]. These authors also advanced an alternative hypothesis concerning the origin of the TAT-C allele. Specifically, high frequency of the ancestral, in respect of the TAT-C allele, Y-chromosome variant LLY22g-A (17%) revealed in Maris is considered to be the evidence of the emergence of the TAT-C allele in this particular population [12]. The presence of the TAT-C allele in the Russian gene pool with frequencies varying from 15 to 21% is explained by the presence of considerable proportion of the Finno-Ugric and/or Turkic admixture in the modern Russians [17, 27].

Since in Tuvinians the tribe attribution is determined down the male lineage, it is thus possible to correlate the information on the origin of certain tribal groups with the Y-chromosome variants. For instance, the carriers of the TAT-C allele in Tuvinian population are the representatives of the Irgit tribe. This allele was found in the five of six members of the tribe examined. In addition, this allele is a marker for Y chromosomes in the representatives of three other tribes, namely, the Turkic by its origin Oorzhak tribe and two Mongolian tribes (Salchak and Mongush). Thereby, TAT-C haplotype in the Tuvinian gene pool may be either of Turkic, or of Mongolian descent. Some authors also suggest the Samoyedic origin of the Irgit tribe [28]. This in turn can serve as a confirmation of the Finno-Ugric origin of the TAT-C allele. The use of a combined approach based on the analysis of Y-chromosome diallelic and microsatellite loci variation along with the inclusion in the analysis of other Turkic and Finno-Ugric populations would provide detailed estimation of the contributions of different by the descent components to the gene pool of the present-day population of the region examined
 


--------------------------------------------------------------------------------

 Some other important points to consider about Tat-C:

- There is, contrary to what one would expect if Tat-C was an exclusive Asiatic marker, no north-south frequency gradient of the Tat C allele from the Lapps to the Lithuanians; instead there is a sharp east-west cline both in Scandinavia and on the Baltic area. (Rootsi et al. 2000: 152).  In other words, if Tat-C was a purely Asiatic marker, its gradient should run from North to South - but it does not, as even the Kittles report (above) showed.

- Mongoloid admixture in NE Europe and Tat-C are two separate, not-necessarily related issues. There is no doubt some Mongoloid admixture in NE Europe (as indicated by the presence of low levels of East Asian mtDNA). But, as Professor Villems has pointed out (above), there is reason to question if Tat-C actually originated in Mongoloids. In addition, Tat-C levels are not well correlated with levels of Mongoloid admixture.

- Even if Tat-C originated in Siberia, this doesn't necessarily mean that it is a Mongoloid trait. As the skeletal evidence has clearly shown, some of the earliest populations of central and western Siberia were not Mongoloid at all, at least in the era prior to the expansion of Mongoloid races from the Far East.

- Tat-C is associated with both NE Europeans and Arctic Asians. Similarly, haplogroup HG26, ancestral to HG1, is found at very low levels in western Europeans, and relatively high levels in some Mongoloid groups. But this doesn't mean western Europeans are descended from Mongoloids. It means that Mongoloids and Europeans share a common male ancestor, and that a Y-chromosome with a newer mutation came to dominate among western Europeans.

CONCLUSION

In conclusion then, there are three potential scenarios to be drawn from this welter of evidence:

(1) Some northeastern Europeans descend almost totally from cold-adapted 'Caucasoids', any Mongoloid admixture being insignificant enough to have little effect on their phenotype;

(2) Some northeastern Europeans are a mix of 'Caucasoids' and an archaic Central Asian type intermediate between 'Caucasoids' and Mongoloids;

(3) Some northeastern Europeans derive large amounts of their ancestry from both 'Caucasoids' and evolved Mongoloids.

Based on current evidence, scenario (1) seems the most likely, although scenario (2) could also be possible. Scenario (3), although favored by those unfamiliar with the research around the dubious origins of Tat-C, is increasingly considered unlikely, and northeastern European pigmentation argues against significant Mongoloid admixture (and certainly rules out large amounts of recent Mongoloid admixture).

Finally, the reader is referred to a study by Guglielmino et. al., who found that Finns have a maximum 10% "Uralic" admixture, a number obtained by comparing Finns to Europeans and to some majority Caucasoid Uralic-speaking populations. Even this does not imply that Finns are 10 percent Mongoloid, merely that Finns are genetically closer to the Caucasoid component of some of the other "Uralic" groups than are most Europeans.

http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=2221031&dopt=Abstract

 
1: Am J Phys Anthropol. 1990 Sep;83(1):57-68
Uralic genes in Europe.

Guglielmino CR, Piazza A, Menozzi P, Cavalli-Sforza LL.

Dipartimento di Genetica e Microbiologia, Universita di Pavia, Italy.

We have analysed data of three European populations speaking non-Indoeuropean languages: Hungarians, Lapps, and Finns. Principal coordinate analysis shows that Lapps are almost exactly intermediate between people located geographically near the Ural mountains and speaking Uralic languages, and central and northern Europeans. Hungarians and Finns are definitely closer to Europeans. An analysis of genetic admixture between Uralic and European ancestors shows that Lapps are slightly more than 50% European, Hungarians are 87% European, and Finns are 90% European. There is basic agreement between these conclusions and historical data on Hungary. Less is known about Finns and very little about Lapps.

PMID: 2221031 [PubMed - indexed for MEDLINE
 


Offline BabylonianJew

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Re: Racial Admixture in various European Populations
« Reply #7 on: May 15, 2007, 11:58:17 PM »
Whose going to read such a long thread? Why don't you at least put pictures?



I will later.

Offline ScotcH

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Re: Racial Admixture in various European Populations
« Reply #8 on: June 19, 2007, 08:58:57 AM »
 SCHVARTZE-Lovers !  You the reason why BLAXXX get they Welfair !!

And are running society into the Ground !!  Wake up !
SUBMISSION IS DEATH !

newman

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Re: Racial Admixture in various European Populations
« Reply #9 on: June 19, 2007, 11:01:54 AM »
Amazing research on northern european bloodlines:.......

The dutch came into existance when german hog farmers started sleeping with their livestock. :laugh:

Offline JustaGreek

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Re: Racial Admixture in various European Populations
« Reply #10 on: March 09, 2010, 02:48:04 PM »
This is test is known to most for being biased and sponsored by individuals from FYROM who have a deep hatred for Greeks because we are not allowing them to steal our history.  If one studies most of the names on their they would be surprised on what country they come from.

Arnaiz-Villena A, Dimitroski K, Pacho A, Moscoso J, Gómez-Casado E, Silvera-Redondo C, Varela P, Blagoevska M, Zdravkovska V, Martínez-Laso J.

Here is what happen to Arnaiz Villena's so called test.  Also note what he wrote regarding the Jewish people and the muslim palestinians.

Quote
Dropped genetics paper lacked scientific merit
Nature 415, 115 (10 January 2002); doi:10.1038/415115b

Sir – Even though the controversial withdrawal of a paper on the genetic relatedness of Palestinians and Jews by the journal Human Immunology (see Nature 414, 382; 2001 (Nature Publishing Group - Citation Results)) is a minor episode compared with the tragedies caused by ethnic/religious conflicts over past decades, the issues involved are worth revisiting.

The stated purpose of the paper by Antonio Arnaiz-Villena et al. was to "examine the genetic relationships between the Palestinians and their neighbours (particularly the Jews) in order to: (1) discover the Palestinian origins, and (2) explain the historic basis of the present ... conflict between Palestinians and other Muslim countries with Israelite Jews".

They conclude: "Jews and Palestinians share a very similar HLA genetic pool that supports a common ancient Canaanite origin. Therefore, the origin of the long-lasting Jewish–Palestinian hostility is the fight for land in ancient times."

It is difficult to believe that knowledge of genes may help to explain the present conflict. Although population genetics can address issues of relatedness of populations, mating patterns, migrations and so on, obviously it cannot provide evidence about reasons for conflicts between people.

Our primary concern, however, is that the authors might be perceived to have been discriminated against for political, as opposed to legitimate scientific, reasons.

Even a cursory look at the paper's diagrams and trees immediately indicates that the authors make some extraordinary claims. They used a single genetic marker, HLA DRB1, for their analysis to construct a genealogical tree and map of 28 populations from Europe, the Middle East, Africa and Japan. Using results from the analysis of a single marker, particularly one likely to have undergone selection, for the purpose of reconstructing genealogies is unreliable and unacceptable practice in population genetics.

The limitations are made evident by the authors' extraordinary observations that Greeks are very similar to Ethiopians and east Africans but very distant from other south Europeans; and that the Japanese are nearly identical to west and south Africans. It is surprising that the authors were not puzzled by these anomalous results, which contradict history, geography, anthropology and all prior population-genetic studies of these groups. Surely the ordinary process of refereeing would have saved the field from this dispute.

We believe that the paper should have been refused for publication on the simple grounds that it lacked scientific merit.

Neil Risch
Department of Genetics, Stanford University School of Medicine, Stanford, California 94305, USA

Alberto Piazza
Department of Genetics, Biology and Biochemistry, University of Torino, Via Santena 19, 10126 Torino, Italy

L. Luca Cavalli-Sforza
Department of Genetics, Stanford University School of Medicine, Stanford, California 94305, USA


http://www.nature.com/nature/journal/v415/n6868/full/415115b.html
http://www.ncbi.nlm.nih.gov/pubmed/11543891?dopt=Abstract
http://racialreality.blogspot.com/2004/09/study-clarification-ii.html

Offline Kahane-Was-Right BT

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Re: Racial Admixture in various European Populations
« Reply #11 on: March 09, 2010, 03:18:00 PM »
Interesting post, Just a greek.  I was about to say how odd that this bizarre thread got bumped today, several years later, but to correct such an egregious error I am glad you bumped it!   What he ("Babylonian Jew") was presenting was not science but polemics, it seems.

I am curious though, who is out to steal the Greek history or deny you the history?   Excuse my ignorance of modern Greek affairs.

Moshe92

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Re: Racial Admixture in various European Populations
« Reply #12 on: March 09, 2010, 03:21:27 PM »
Babylonian Jew was banned a long time ago. He looks like quite a nut.  :::D

Offline JustaGreek

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Re: Racial Admixture in various European Populations
« Reply #13 on: March 09, 2010, 05:33:21 PM »
Interesting post, Just a greek.  I was about to say how odd that this bizarre thread got bumped today, several years later, but to correct such an egregious error I am glad you bumped it!   What he ("Babylonian Jew") was presenting was not science but polemics, it seems.

I am curious though, who is out to steal the Greek history or deny you the history?   Excuse my ignorance of modern Greek affairs.

We Greeks have been having an issue with a Slavic people that refer to themselves as Macedonians when in fact they are nothing of the sort.  They are a mixture of Serbian and Bulgarians.  They claim to be directly related to Alexander the Great and that the ancient Macedonians were not Greek at all.  They have been doing many different things to try to discredit the Greeks in any way possible to make us look at bad.  They work together with the filthy muslim turks aswell.   Its a very long story. I can go on and on..