Haplogroup I-M438
 | This article needs attention from an expert in Human Genetic History. The specific problem is: Nomenclature of haplogroup(s) and subclades. (November 2015) |
| Haplogroup I-M438 | |
|---|---|
| Possible time of origin | 28–33,000 years ago[1] |
| Possible place of origin | South-Eastern or Eastern Europe. |
| Ancestor | I-M170 |
| Descendants | I-L460, I-L1251 |
| Defining mutations | M438/P215/S31 |
| Highest frequencies | I2a1a: Sardinia[2]
I2a1b: Bosnia and Herzegovina,[3] I2a2: Britain, Germany, and Sweden[2] |
Haplogroup I-M438, also known as I2 (ISOGG 2019), is a human DNA Y-chromosome haplogroup, a subclade of haplogroup I-M170. Haplogroup I-M438 originated some time around 26,000–31,000 BCE. It originated in Europe and developed into several main subgroups: I2-M438*, I2a-L460, I2b-L415 and I2c-L596.[2] The haplogroup can be found all over Europe and reaches its maximum frequency in the Dinaric Alps (Balkans) via founder effect, related to the migrations of the Early Slavs to the Balkan peninsula.
The oldest example so far found is that of Hohle Fels (49) from Germany, being at least 14,200 years old.[4]
Origin and prehistoric presence
[edit]![[icon]](/wiki/File:Wiki_letter_w_cropped.svg){kind=small} | This section needs expansion. You can help by adding to it. (April 2017) |
Haplogroup I2a was the most frequent Y-DNA among Mesolithic Western European hunter-gatherers (WHG) belonging to Villabruna Cluster. A 2015 study found haplogroup I2a in 13,500 year old remains from the Azilian culture (from Grotte du Bichon, modern Switzerland).[5] Subclades of I2a1 (I-P37.2), namely I-M423 and I-M26, have been found in remains of WHGs dating from 10,000 to 8,000 years before present.[6]
In a 2015 study published in Nature, the remains of six individuals from Motala ascribed to the Kongemose culture were successfully analyzed. With regards to Y-DNA, two individuals were ascribed to haplogroup I2a1b, one individual was ascribed to haplogroup I2a1, and one individual was ascribed to haplogroup I2c.[7]
Subclades of I-L460
[edit]I-P37.2
[edit]The I-P37.2+ (also known as I2a1a) (ISOGG 2019). The subclade divergence for I-P37.2 occurred 10.7±4.8 kya. The age of YSTR variation for the P37.2 subclade is 8.0±4.0 kya.[2] It is the predominant version of I2 in Eastern Europe.[8] The I2a is further made up by subgroups I-M26, I-M423, I-L1286, I-L880.
I-L158
[edit]Haplogroup I-M26 (or M26) I2a1a1a (ISOGG 2019).
Haplogroup I-L158 (L158, L159.1/S169.1, M26) accounts for approximately 40% of all patrilines among Sardinians.[9][10] It is also found at low to moderate frequency among populations of the Pyrenees (9.5% in Bortzerriak, Navarra; 9.7% in Chazetania, Aragon; 8% in Val d'Aran, Catalunya; 2.9% in Alt Urgell, Catalunya; and 8.1% in Baixa Cerdanya, Catalunya) and Iberia, and it has been found in 1.6% of a sample of Albanians living in the Republic of North Macedonia[11] and 1.2% (3/257) of a sample of Czechs.[12] The age of YSTR variation for the M26 subclade has been calculated as 8.0±4.0 kya.[2]
I-L178
[edit]I-L178 is very rare, but has been found in two persons from Germany and one from Poland. The age of YSTR variation for the M423 subclade is 8.8±3.6 kya.[1]
I2a-L621
[edit]
I2a1a2b-L621 is typical of the Slavic populations, being highest in Southeastern European regions of Bosnia-Herzegovina and South Croatia (>45%),[3][13][14] in Croats (37.7-69.8%), Bosniaks (43.53-52.17%), and Serbs (36.6-42%)—often called "Dinaric".[15] It has the highest variance and concentration in Eastern Europe (i.e., Ukraine, Southeastern Poland, Belarus).[16] According to YFull YTree it formed 11,400 YBP and had TMRCA 6,500 YBP, while its main subclades lineage is I-CTS10936 (6,500-5,600 YBP) > I-S19848 (5,600 YBP) > I-CTS4002 (5,600-5,100 YBP) > I-CTS10228 (5,100-3,400 YBP) > I-Y3120 (3,400-2,100 YBP) > I-Y18331 (2,100 YBP) / I-Z17855 (2,100-1650 YBP) / I-Y4460 (2,100 YBP) / I-S17250 (2,100-1,850 YBP) > I-PH908 (1,850-1,700 YBP).[17]
Older research considered that the high frequency of this subclade in the South Slavic-speaking populations to be the result of "pre-Slavic" paleolithic settlement in the region. Peričić et al. (2005) for instance placed its expansion to have occurred "not earlier than the YD to Holocene transition and not later than the early Neolithic".[2][3][18][19] However, the prehistoric autochthonous origin of the haplogroup I2 in the Balkans is now considered as outdated,[nb 1] as already Battaglia et al. (2009) observed highest variance of the haplogroup in Ukraine, and Zupan et al. (2013) noted that it suggests it arrived with Slavic migration from the homeland which was in present-day Ukraine.[24] O.M. Utevska (2017), in her PhD thesis, despite being a part of research team who came to a different conclusion in 2015,[25] proposed that the haplogroup STR haplotypes have the highest diversity in Ukraine, with ancestral STR marker result "DYS448=20" comprising "Dnieper-Carpathian" cluster, while younger derived result "DYS448=19" comprising the "Balkan cluster" which is predominant among the South Slavs.[16] According to her, this "Balkan cluster" also has the highest variance in Ukraine, which indicates that the very high frequency in the Western Balkan is probably because of a founder effect.[16] Utevska calculated that the STR cluster divergence and its secondary expansion from the middle reaches of the Dnieper river or from Eastern Carpathians towards the Balkan peninsula happened approximately 2,860 ± 730 years ago, relating it to the times before Slavs, but much after the decline of the Cucuteni–Trypillia culture.[16] However, STR-based calculations give overestimated dates,[26][27] and more specifically, the "Balkan cluster" is represented by a single SNP, I-PH908, known as I2a1a2b1a1a1c in ISOGG phylogenetic tree (2019), and according to YFull YTree it formed and had TMRCA approximately 1,850-1,700 YBP (2nd-3rd century AD).[17]
It is considered that I-L621 could have been present in the Cucuteni–Trypillia culture,[28] but until now was mainly found G2a and non-I2-L621 clades,[29][30] and another clade I2a1a1-CTS595 was present in the Baden culture of the Chalcolithic Carpathian Basin.[28][31][32] Although it is dominant among the modern Slavic peoples on the territory of the former Balkan provinces of the Roman Empire, until now it was not found among the samples from the Roman period and is almost absent in contemporary population of Italy.[15] According to Pamjav et al. (2019) and Fóthi et al. (2020), the distribution of ancestral subclades like of I-CTS10228 among contemporary carriers indicates a rapid expansion from Southeastern Poland, is mainly related to the Slavs and their medieval migration, and the "largest demographic explosion occurred in the Balkans".[15][33] According to a 2023 archaeogenetic study, I2a-L621 is absent in the antiquity and appears only since the Early Middle Ages "always associated with Eastern European related ancestry in the autosomal genome, which supports that these lineages were introduced in the Balkans by Eastern European migrants during the Early Medieval period."[34]
Some of the earliest archeogenetic samples until now is Sungir 6 (~900 YBP) near Vladimir, Russia which belonged to the I-S17250 > I-Y5596 > I-Z16971 > I-Y5595 > I-A16681 subclade,[35][36] as well I-CTS10228 and I-Y3120 subclades found in two Vikings from Sweden (VK53) and Ukraine (VK542) with predominantly Slavic ancestry of which the second belongs to Gleb Svyatoslavich (11th century).[37] It was also found in the skeletal remains of Hungarian conquerors of the Carpathian Basin from the 9th century, part of Western Eurasian-Slavic component of the Hungarians.[15][28][38]
I-M223
[edit]Haplogroup I-M223 aka I2a1b1 (ISOGG 2019), formerly I2a2a (ISOGG 2014). The age of YSTR variation for the I-M223 subclade has been variously estimated as 13.2±2.7 kya,[2] 12.3±3.1 kya.,[1] 14.6 kya[39] and 14.6±3.8 kya (Rootsi 2004). I-M223 has a peak in Germany and another in the northeast of Sweden, but also appears in Romania/Moldova, Russia, Greece, Italy and around the Black Sea.[40] Haplogroup I-M223 has been found in over 4% of the population only in Germany, the Netherlands, Belgium, Denmark, Scotland, and England (excluding Cornwall) – also the southern tips of Sweden and Norway in Northwest Europe; the provinces of Normandy, Maine, Anjou, and Perche in northwestern France; the province of Provence in southeastern France; the regions of Tuscany, Umbria, and Latium in Italy; Moldavia and the area around Russia's Ryazan Oblast and Mordovia in Eastern Europe. Of historical note, both haplogroups I-M253 and I-M223 appear at a low frequency in the historical regions of Bithynia and Galatia in Turkey. Haplogroup I-M223 also occurs among approximately 1% of Sardinians.
I-M284
[edit]Haplogroup I2a1b1a1a (ISOGG 2019) or I-M284, has been found almost exclusively amongst the populations of the United Kingdom and Ireland suggesting that it may have arisen amongst the Ancient Britons, with a most recent common ancestor (MRCA) who lived about 3,100 years BP.[41] The presence of this subclade "provides some tentative evidence of ancient flow with eastern areas that could support the idea that the [late Celtic] La Tene culture was accompanied by some migration."[42]
Where it is found in those of predominately Irish descent, with Gaelic surnames, it may suggest an ancestor who arrived in Ireland during prehistory, from Celtic Britain.[42] For example, I-M284 includes many males with the surnames McGuinness and McCartan, who have a single, historically recorded male ancestor in the 6th century; thus it is unlikely to be the result of subsequent migration from Britain to Ireland.[42] Some subclades of I-M284 that are atypical of Ireland are relatively common in continental Europe,[42] which also supports a point of origin east of Ireland.
I-CTS10057
[edit]Continentals. Mother Haplogroup for group I-Z161 (Continental 1 and 2) and I-L701 group (Continental 3). Around 10.000 years old.
I-Z161
[edit]Haplogroup I2a1b1a2b (ISOGG 2019). Z161+ defines the I2 Continental clade 1 and 2. Its age is estimated around 7,000 years old. It is mainly found in North Europe, especially in Denmark, Germany, the Netherlands, and England. In Northwest Sicily it can also be found; this is believed to be due to remnants of a Norman settlement.
I-L701
[edit]Called Continental 3. Continental 3 has a wide distribution. Found in Central Europe from Germany, Austria to Poland, Romania and Ukraine, but also in lower frequencies in Greece, Italy, France, Spain, England, Ireland, and Armenia. It may have been disseminated in part by the Goths. It is nearly absent from Scandinavia and Scotland.
I-M436
[edit] | This section needs expansion. You can help by adding to it. (January 2021) |
Subclades list
[edit] |
Up-to-date phylogenetic trees listing subclades of I can be found at Y-Full and FamilyTreeDNA
Subclades list
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See also
[edit]Notes
[edit]- ^ The SNP I-P37 itself formed approximately 21,000 YBP and had TMRCA 18,400 YBP according to YFull YTree,[20] being too old and widespread as an SNP for argumentation of ancient autochthony or medieval migration as well the old research used outdated nomenclature. According to "I-P37 (I2a)" project at Family Tree DNA, the divergence at STR marker DYS448 20 > 19 is reported since 2007,[21] while the SNP which defines the STR Dinaric-South cluster, I-PH908, is reported since 2014.[22] The SNP I-PH908 at ISOGG phylogenetic tree is named as I2a1a2b1a1a1c,[23] while formed and had TMRCA approximately 1,800 YBP according to YFull.[17]
References
[edit]- ^ a b c Underhill PA, Myres NM, Rootsi S, Chow CT, Lin AA, Otillar RP, et al. (2007). "New phylogenetic relationships for Y-chromosome haplogroup I: Reappraising its Phylogeography and Prehistory". In Mellars P, Boyle K, Bar-Yosef O, Stringer C (eds.). Rethinking the Human Evolution. McDonald Institute for Archaeological Research. pp. 33–42. ISBN 978-1-902937-46-5.
- ^ a b c d e f g Rootsi S, Magri C, Kivisild T, Benuzzi G, Help H, Bermisheva M, et al. (July 2004). "Phylogeography of Y-chromosome haplogroup I reveals distinct domains of prehistoric gene flow in europe". American Journal of Human Genetics. 75 (1): 128–137. doi:10.1086/422196. PMC 1181996. PMID 15162323.
- ^ a b c Pericić M, Lauc LB, Klarić IM, Rootsi S, Janićijevic B, Rudan I, et al. (October 2005). "High-resolution phylogenetic analysis of southeastern Europe traces major episodes of paternal gene flow among Slavic populations". Molecular Biology and Evolution. 22 (10): 1964–1975. doi:10.1093/molbev/msi185. PMID 15944443.
- ^ Posth, Cosimo; Yu, He; Ghalichi, Ayshin; Rougier, Hélène; Crevecoeur, Isabelle; Huang, Yilei; Ringbauer, Harald; Rohrlach, Adam B.; Nägele, Kathrin; Villalba-Mouco, Vanessa; Radzeviciute, Rita; Ferraz, Tiago; Stoessel, Alexander; Tukhbatova, Rezeda; Drucker, Dorothée G. (2023-03-01). "Palaeogenomics of Upper Palaeolithic to Neolithic European hunter-gatherers". Nature. 615 (7950): 117–126. doi:10.1038/s41586-023-05726-0. hdl:10256/23099. ISSN 1476-4687. PMC 9977688. PMID 36859578.
- ^ Jones ER, Gonzalez-Fortes G, Connell S, Siska V, Eriksson A, Martiniano R, et al. (November 2015). "Upper Palaeolithic genomes reveal deep roots of modern Eurasians". Nature Communications. 6: 8912. Bibcode:2015NatCo...6.8912J. doi:10.1038/ncomms9912. PMC 4660371. PMID 26567969.
- ^ [1] Archived 2017-04-30 at the Wayback Machine Mesolithic Western Eurasian DNA
- ^ Mathieson I, Lazaridis I, Rohland N, Mallick S, Patterson N, Roodenberg SA, et al. (December 2015). "Genome-wide patterns of selection in 230 ancient Eurasians". Nature. 528 (7583): 499–503. Bibcode:2015Natur.528..499M. doi:10.1038/nature16152. PMC 4918750. PMID 26595274.
- ^ Sazzini M, Sarno S, Luiselli D (2014). "The Mediterranean Human Population: An Anthropological Genetics Perspective". The Mediterranean Sea. pp. 529–551. doi:10.1007/978-94-007-6704-1_31. ISBN 978-94-007-6703-4.
- ^ Rootsi S (31 December 2006). "Y-Chromosome haplogroup I prehistoric gene flow in Europe". Documenta Praehistorica. 33: 17–20. doi:10.4312/dp.33.3.
- ^ Francalacci P, Morelli L, Angius A, Berutti R, Reinier F, Atzeni R, et al. (August 2013). "Low-pass DNA sequencing of 1200 Sardinians reconstructs European Y-chromosome phylogeny". Science. 341 (6145): 565–569. Bibcode:2013Sci...341..565F. doi:10.1126/science.1237947. PMC 5500864. PMID 23908240.
- ^ Battaglia V, Fornarino S, Al-Zahery N, Olivieri A, Pala M, Myres NM, et al. (June 2009). "Y-chromosomal evidence of the cultural diffusion of agriculture in Southeast Europe". European Journal of Human Genetics. 17 (6): 820–830. doi:10.1038/ejhg.2008.249. PMC 2947100. PMID 19107149.
- ^ Luca F, Di Giacomo F, Benincasa T, Popa LO, Banyko J, Kracmarova A, et al. (January 2007). "Y-chromosomal variation in the Czech Republic". American Journal of Physical Anthropology. 132 (1): 132–139. doi:10.1002/ajpa.20500. hdl:2108/35058. PMID 17078035.
- ^ Mršić G, Gršković B, Vrdoljak A, Popović M, Valpotić I, Anđelinović Š, et al. (July 2012). "Croatian national reference Y-STR haplotype database". Molecular Biology Reports. 39 (7): 7727–7741. doi:10.1007/s11033-012-1610-3. PMID 22391654. S2CID 18011987.
- ^ Kovacevic L, Tambets K, Ilumäe AM, Kushniarevich A, Yunusbayev B, Solnik A, et al. (2014). "Standing at the gateway to Europe--the genetic structure of Western balkan populations based on autosomal and haploid markers". PLOS ONE. 9 (8): e105090. Bibcode:2014PLoSO...9j5090K. doi:10.1371/journal.pone.0105090. PMC 4141785. PMID 25148043.
- ^ a b c d Fóthi E, Gonzalez A, Fehér T, Gugora A, Fóthi Á, Biró O, Keyser C (2020). "Genetic analysis of male Hungarian Conquerors: European and Asian paternal lineages of the conquering Hungarian tribes". Archaeological and Anthropological Sciences. 12 (1). doi:10.1007/s12520-019-00996-0.
We looked at 16 loci from 640 I2a-L621 samples in FTDNA's I2a project database and found that 7 individuals were 2 genetic steps away the Karos samples, of whom 1 was a Hungarian from Kunszentmárton, 2 were Ukrainians, 1 was Lithuanian, 1 was Belarusian, 1 was Russian, and 1 was a German from Poland. Based on SNP analysis, the CTS10228 group is 2200 ± 300 years old. The group's demographic expansion may have begun in Southeast Poland around that time, as carriers of the oldest subgroup are found there today. The group cannot solely be tied to the Slavs, because the proto-Slavic period was later, around 300–500 CE ... The SNP-based age of the Eastern European CTS10228 branch is 2200 ± 300 years old. The carriers of the most ancient subgroup live in Southeast Poland, and it is likely that the rapid demographic expansion which brought the marker to other regions in Europe began there. The largest demographic explosion occurred in the Balkans, where the subgroup is dominant in 50.5% of Croatians, 30.1% of Serbs, 31.4% of Montenegrins, and in about 20% of Albanians and Greeks. As a result, this subgroup is often called Dinaric. It is interesting that while it is dominant among modern Balkan peoples, this subgroup has not been present yet during the Roman period, as it is almost absent in Italy as well (see Online Resource 5; ESM_5). ... Their genetic haplogroup, I2a-CTS10228, is widespread among Slavs, but it is only present in 7% of Caucasian peoples, namely among the Karachay ... As such, it appears that the I2a-CTS10228 haplogroup in the paternal lineage of the Karos leaders arises from a specific branch in the Northern Caucasus dating to about 400–500 CE. Its modern descendents live among the Karachay, Hungarians, and various other surrounding nationalities.
- ^ a b c d O.M. Utevska (2017). Генофонд українців за різними системами генетичних маркерів: походження і місце на європейському генетичному просторі [The gene pool of Ukrainians revealed by different systems of genetic markers: the origin and statement in Europe] (PhD) (in Ukrainian). National Research Center for Radiation Medicine of National Academy of Sciences of Ukraine. pp. 219–226, 302.
- ^ a b c "I-PH908 YTree v8.06.01". YFull.com. 27 June 2020. Retrieved 17 July 2020.
- ^ Marjanovic D, Fornarino S, Montagna S, Primorac D, Hadziselimovic R, Vidovic S, et al. (November 2005). "The peopling of modern Bosnia-Herzegovina: Y-chromosome haplogroups in the three main ethnic groups". Annals of Human Genetics. 69 (Pt 6): 757–763. doi:10.1111/j.1529-8817.2005.00190.x. PMID 16266413. S2CID 36632274.
- ^ Rębała K, Mikulich AI, Tsybovsky IS, Siváková D, Džupinková Z, Szczerkowska-Dobosz A, Szczerkowska Z (16 March 2007). "Y-STR variation among Slavs: evidence for the Slavic homeland in the middle Dnieper basin". Journal of Human Genetics. 52 (5): 406–414. doi:10.1007/s10038-007-0125-6. PMID 17364156.
- ^ "I-P37 YTree v8.06.01". YFull.com. 27 June 2020. Retrieved 17 July 2020.
- ^ "I2a Y-Haplogroup - Results: I2a2a-Dinaric". Family Tree DNA. Retrieved 11 November 2018.
Ken Nordtvedt has split I2a2-M423-Dinaric into Din-N and Din-S. Din-N is older than Din-S. N=north of the Danube and S=south of the Danube River ... May 8, 2007: Dinaric I1b1 and DYS 448. DYS448 19 for S and 20 for N.
- ^ Bernie Cullen (22 August 2016). "Link to I-L621 tree showing major STR clusters (Updated)". i2aproject.blogspot.com. Blogger. Retrieved 3 April 2019.
- ^ "Y-DNA Haplogroup I and its Subclades - 2019-2020". ISOGG. 1 October 2019. Retrieved 17 July 2020.
- ^ Zupan A, Vrabec K, Glavač D (2013). "The paternal perspective of the Slovenian population and its relationship with other populations". Annals of Human Biology. 40 (6): 515–526. doi:10.3109/03014460.2013.813584. PMID 23879710. S2CID 34621779.
- ^ Kushniarevich, Alena; Utevska, Olga; Chuhryaeva, Marina; Agdzhoyan, Anastasia; Dibirova, Khadizhat; Uktveryte, Ingrida; Möls, Märt; Mulahasanovic, Lejla; Pshenichnov, Andrey; Frolova, Svetlana; Shanko, Andrey; Metspalu, Ene; Reidla, Maere; Tambets, Kristiina; Tamm, Erika (2015-09-02). Calafell, Francesc (ed.). "Genetic Heritage of the Balto-Slavic Speaking Populations: A Synthesis of Autosomal, Mitochondrial and Y-Chromosomal Data". PLOS ONE. 10 (9): e0135820. Bibcode:2015PLoSO..1035820K. doi:10.1371/journal.pone.0135820. ISSN 1932-6203. PMC 4558026. PMID 26332464.
- ^ Šarac J, Šarić T, Havaš Auguštin D, Novokmet N, Vekarić N, Mustać M, et al. (November 2016). "Genetic heritage of Croatians in the Southeastern European gene pool-Y chromosome analysis of the Croatian continental and Island population". American Journal of Human Biology. 28 (6): 837–845. doi:10.1002/ajhb.22876. PMID 27279290. S2CID 25873634.
It is important to stress that the proposed old age of the I2a1b-M423 and R1a1a1b1a*-M558 lineages obtained in previous studies (Battaglia et al., 2009; Peričić et al., 2005; Rootsi et al., 2004; Underhill et al., 2007, 2015) has been based on STR analysis (8 and 10 loci, respectively) and recent studies clearly indicate that the STR-based age calculations tend to yield overestimated dates (Batini et al., 2015; Hallast et al., 2015; Karmin et al., 2015).
- ^ Balanovsky O (May 2017). "Toward a consensus on SNP and STR mutation rates on the human Y-chromosome". Human Genetics. 136 (5): 575–590. doi:10.1007/s00439-017-1805-8. PMID 28455625. S2CID 3714493.
While the reasons for the difference between genealogical and evolutionary Y-STR rates are thus partly understood, it remains unclear which rate to use. Many have applied the evolutionary rate, though quite a few have used the genealogical, or both, rates. Genetic genealogists generally apply the genealogical rate and criticize population-genetic studies for reporting (in their view) three-times overestimated ages ... The age of each haplogroup was also calculated using the STR genealogical rate and the STR evolutionary rate. Confidence intervals for the two STR-based ages (not shown on the plot) do not overlap. For example, the genealogical age of I2a-L621 (2200 ± 500 years) reaches the envelope age (from 2600 to 3100 ages), while the evolutionary age lies far beyond (9900 ± 2700 years). The observed pattern (Fig. 2a) clearly differs for haplogroups of different age classes. For ages less than 7000 years, the genealogical STR rate provides results consistent with or slightly underestimating the "true" ages, while the evolutionary rate results in three-fold overestimates. For ages between roughly 7000 and 15,000 years neither STR rate provides correct results. For haplogroups older than 15,000 years, the evolutionary rate estimates correctly or overestimates the "true" age.
- ^ a b c Neparáczki E, Maróti Z, Kalmár T, Maár K, Nagy I, Latinovics D, et al. (November 2019). "Y-chromosome haplogroups from Hun, Avar and conquering Hungarian period nomadic people of the Carpathian Basin". Scientific Reports. 9 (1). Nature Research: 16569. Bibcode:2019NatSR...916569N. doi:10.1038/s41598-019-53105-5. PMC 6851379. PMID 31719606.
Hg I2a1a2b-L621 was present in 5 Conqueror samples, and a 6th sample form Magyarhomorog (MH/9) most likely also belongs here, as MH/9 is a likely kin of MH/16 (see below). This Hg of European origin is most prominent in the Balkans and Eastern Europe, especially among Slavic speaking groups. It might have been a major lineage of the Cucuteni-Trypillian culture and it was present in the Baden culture of the Calcholitic Carpathian Basin24 ... The identical I2a1a2b Hg-s of Magyarhomorog individuals appears to be frequent among high-ranking Conquerors, as the most distinguished graves in the Karos2 and 3 cemeteries also belong to this lineage.
- ^ Mathieson I, Alpaslan-Roodenberg S, Posth C, Szécsényi-Nagy A, Rohland N, Mallick S, et al. (March 2018). "The genomic history of southeastern Europe". Nature. 555 (7695): 197–203. Bibcode:2018Natur.555..197M. doi:10.1038/nature25778. PMC 6091220. PMID 29466330.
- ^ Gelabert P, Schmidt RW, Fernandes DM, Karsten JK, Harper TK, Madden GD, et al. (May 2022). "Genomes from Verteba cave suggest diversity within the Trypillians in Ukraine". Scientific Reports. 12 (1). Nature Research: 7242. Bibcode:2022NatSR..12.7242G. doi:10.1038/s41598-022-11117-8. PMC 9068698. PMID 35508651.
- ^ Lipson M, Szécsényi-Nagy A, Mallick S, Pósa A, Stégmár B, Keerl V, et al. (November 2017). "Parallel palaeogenomic transects reveal complex genetic history of early European farmers". Nature. 551 (7680): 368–372. Bibcode:2017Natur.551..368L. doi:10.1038/nature24476. PMC 5973800. PMID 29144465.
- ^ Patterson N, Isakov M, Booth T, Büster L, Fischer CE, Olalde I, et al. (January 2022). "Large-scale migration into Britain during the Middle to Late Bronze Age". Nature. 601 (7894): 588–594. Bibcode:2022Natur.601..588P. doi:10.1038/s41586-021-04287-4. PMC 8889665. PMID 34937049. S2CID 245509501.
- ^ Pamjav H, Fehér T, Németh E, Koppány Csáji L (2019). Genetika és őstörténet (in Hungarian). Napkút Kiadó. p. 58. ISBN 978-963-263-855-3.
Az I2-CTS10228 (köznevén „dinári-kárpáti") alcsoport legkorábbi közös őse 2200 évvel ezelőttre tehető, így esetében nem arról van szó, hogy a mezolit népesség Kelet-Európában ilyen mértékben fennmaradt volna, hanem arról, hogy egy, a mezolit csoportoktól származó szűk család az európai vaskorban sikeresen integrálódott egy olyan társadalomba, amely hamarosan erőteljes demográfiai expanzióba kezdett. Ez is mutatja, hogy nem feltétlenül népek, mintsem családok sikerével, nemzetségek elterjedésével is számolnunk kell, és ezt a jelenlegi etnikai identitással összefüggésbe hozni lehetetlen. A csoport elterjedése alapján valószínűsíthető, hogy a szláv népek migrációjában vett részt, így válva az R1a-t követően a második legdominánsabb csoporttá a mai Kelet-Európában. Nyugat-Európából viszont teljes mértékben hiányzik, kivéve a kora középkorban szláv nyelvet beszélő keletnémet területeket.
- ^ Olalde, Iñigo; Carrión, Pablo (December 7, 2023). "A genetic history of the Balkans from Roman frontier to Slavic migrations". Cell. 186 (25): P5472–5485.E9. doi:10.1016/j.cell.2023.10.018. PMC 10752003. PMID 38065079.
- ^ Sikora M, Seguin-Orlando A, Sousa VC, Albrechtsen A, Korneliussen T, Ko A, et al. (November 2017). "Ancient genomes show social and reproductive behavior of early Upper Paleolithic foragers". Science. 358 (6363): 659–662. Bibcode:2017Sci...358..659S. doi:10.1126/science.aao1807. PMID 28982795.
- ^ "I-A16681 YTree v8.06.01". YFull.com. 27 June 2020. Retrieved 17 July 2020.
- ^ Margaryan A, Lawson DJ, Sikora M, Racimo F, Rasmussen S, Moltke I, et al. (September 2020). "Population genomics of the Viking world". Nature. 585 (7825): 390–396. Bibcode:2020Natur.585..390M. bioRxiv 10.1101/703405. doi:10.1038/s41586-020-2688-8. hdl:10852/83989. PMID 32939067. S2CID 221769227.
- ^ Maróti Z, Neparáczki E, Schütz O, Maár K, Varga GI, Kovács B, et al. (July 2022). "The genetic origin of Huns, Avars, and conquering Hungarians". Current Biology. 32 (13): 2858–2870.e7. doi:10.1016/j.cub.2022.04.093. PMID 35617951. S2CID 249050620.
It is notable that the European Y-Hg I2a1a2b1a1a was also specific for the Conqueror group, especially for the elite as also shown before,34 very often accompanied by Asian maternal lineages, indicating that I2a1a2b1a1a could be more typical for the immigrants than to the local population.
- ^ "I-M223 YTree".
- ^ Chiaroni J, Underhill PA, Cavalli-Sforza LL (December 2009). "Y chromosome diversity, human expansion, drift, and cultural evolution". Proceedings of the National Academy of Sciences of the United States of America. 106 (48): 20174–20179. Bibcode:2009PNAS..10620174C. doi:10.1073/pnas.0910803106. PMC 2787129. PMID 19920170.
- ^ YFull, 2021, I-M284
- ^ a b c d McEvoy BP, Bradly DG (2010). "Irish Genetics and Celts". In Cunliffe BW, Koch JT (eds.). Celtic from the West: Alternative Perspectives from Archaeology, Genetics, Language, and Literature. Oxbow Books. pp. 107–120. ISBN 978-1-84217-410-4.
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