The Afontova Gora complex consists of multiplestratigraphic layers, of five or more campsites.[2] The campsites shows evidence ofmammoth hunting and were likely the result of an eastward expansion of mammoth hunters.[3] The human fossils discovered at Afontova Gora, a male and a girl dated to 17,000~15,000 years BP, were stored in theHermitage Museum.[2]
Afontova Gora I is situated on the western bank of the Yenisey River and has yielded the remains from horse, mammoth, reindeer, steppe bison, and large canids. A canid tibia has been dated 16,900 years old and the skull has been taxonomically described as being that of a dog, but it is now lost. Its description falls outside of the range of Pleistocene or modern northern wolves.[4]
Afontova Gora II is the site where the human fossil remains were found. The site was first excavated in 1912-1914 by V.I. Gromov.[5] In 1924, G.P. Sosnovsky, N.K. Auerbach, and V.I. Gromov discovered the first human fossils at the site.[6] The remains of mammoth, Arctic fox, Arctic hare, reindeer, bison, and horse were discovered at the site.[7][8]
Afontova Gora II consists of 7 layers.[8] Layer 3 from Afontova Gora II is the most significant: the layer produced the largest amount of cultural artefacts and is the layer where the human fossil remains were discovered.[9] Over 20,000 artefacts were discovered at layer 3: this layer produced over 450 tools and over 250 osseous artefacts (bone, antler, ivory).[9] The fossils of two distinct individuals were discovered in the initial excavations: the upper premolar of an 11-15 year-old child and the left radius, ulna, humerus, phalanx, and frontal bone of an adult.[9]
Afontova Gora III is the site where the initial excavation was undertaken by Ivan Savenkov in 1884.[5] The site was disturbed by mining activities in the late 1880s.[10] The site consists of 3 layers.[10]
Afontova Gora V was discovered in 1996.[11] The remains of hare, pika, cave lion, horse, reindeer, bison, and partridge were discovered at the site.[12]
The mandibule, teeth and atlas from Afontova Gora, discovered in 2014.[13]
The bodies of two individuals, known asAfontova Gora 2 (AG2) andAfontova Gora 3 (AG3) were discovered within the complex (the name Afontova Gora 1 refers to the remains of acanid).
The human fossil remains ofAfontova Gora 2 were discovered in the 1920s at Afontova Gora II and stored at theHermitage Museum.[2] The remains are dated to around 17,000 BP[14] (16,930-16,490BP[15]).
In 2009, researchers visited the Hermitage Museum and extracted DNA from the humerus ofAfontova Gora 2.[16] Despite significant contamination, researchers succeeded in extractinglow coverage genomes.[14] DNA analysis confirmed that the individual was male.[14]
The individual showed close genetic affinities toMal'ta 1 (Mal'ta boy).[17]Afontova Gora 2 also showed greater genetic affinity for theKaritiana people than for theHan Chinese.[17] Around 1.9-2.7% of the genome was Neanderthal in origin.[15]
Afontova Gora 2 belong to the Y-DNAhaplogroup Q1a1-F746, an uniparental genetic marker that is infrequently observed in modern populations.[18]
Genetic proximity of Afontova Gora with otherAncient North Eurasian populations (Mal'ta andYana), within a principal component analysis of ancient and present-day individuals from worldwide populations.[19]One of the five Afontova Gora teeth of individualAfontova Gora 3 (AG3), dated circa 16,090 cal BC.[20]
In 2014, more human fossil remains were discovered at Afontova Gora II duringsalvage excavation before the construction of a new bridge over the Yenesei River.[15] The remains belonged to two different females: theatlas of an adult female and the mandible and five lower teeth of a teenage girl (Afontova Gora 3) estimated to be around 14–15 years old.[6] Initially, the new findings were presumed to be roughly contemporaneous withAfontova Gora 2.[15] In 2017, directAMS dating revealed thatAfontova Gora 3 is dated to around 16,090 cal BC).[21]
The mandible ofAfontova Gora 3 was described as being gracile.[22]
Researchers analyzing the dental morphology ofAfontova Gora 3 concluded that the teeth showed distinct characteristics with most similarities to another fossil (the Listvenka child) from theAltai-Sayan region and were neither western nor eastern.[23]Afontova Gora 3 and Listvenka showed distinct dental characteristics that were also different from other Siberian fossils, including those from Mal'ta.[24]
DNA was extracted from one of the teeth ofAfontova Gora 3 and analyzed.[15] Compared toAfontova Gora 2, researchers were able to obtainhigher coverage genomes fromAfontova Gora 3.[15] DNA analysis confirmed that the individual was female.[15] mtDNA analysis revealed thatAfontova Gora 3 belonged to themitochondrial Haplogroup R1b.[15] Around 2.9-3.7% of the genome was Neanderthal in origin.[15]
In a 2016 study, researchers determined thatAfontova Gora 2,Afontova Gora 3, andMal'ta 1 (Mal'ta boy) shared common descent and were clustered together in aMal'ta cluster.[15] Genetically,Afontova Gora 3 is not closer toAfontova Gora 2 when compared toMal'ta 1.[15] When compared toMal'ta 1, theAfontova Gora 3 lineage apparently contributed more to modern humans and is genetically closer to Native Americans.[15]
The mutation for blond hair is thought to have originated among the Afontova Gora population of theAncient North Eurasian (ANE) cline of south-central Siberia
Genetic proximity of Afontova Gora 3 with the Tarim mummies
A 2021 genetic study on theTarim mummies found that they were primarily descended from a population represented by theAfontova Gora 3 specimen (AG3), genetically displaying "high affinity" with it.[28] The genetic profile of theAfontova Gora 3 individual represented about 72% of the ancestry of the Tarim mummies, while the remaining 28% of their ancestry was derived fromBaikal EBA (Early Bronze AgeBaikal populations).[29]
The Tarim mummies are thus one of the rareHolocene populations who derive most of their ancestry from theAncient North Eurasians (ANE, specifically theMal'ta and Afontova Gora populations), despite their distance in time (around 14,000 years).[30] More than any other ancient populations, they can be considered as "the best representatives" of the Ancient North Eurasians.[30]
^Vasil'ev, Sergey A. (1992)."The Late Paleolithic of the Yenisei: A New Outline".Journal of World Prehistory.6 (3):337–383.doi:10.1007/BF00980431.ISSN0892-7537.JSTOR25800619.p.337 "At 18,000-16,000 B.P., these were replaced by the Final Paleolithic Afontova and Kokorevo cultures" (...) p.355 "The radiocarbon dates for the cross sections of Afontova Gora II [11,330 B.P. +/ 270 years (Mo-343) and 20,900 B.P. + 300 years (GIN-117)] seem unlikely."
^Germonpré, Mietje; Fedorov, Sergey; Danilov, Petr; Galeta, Patrik; Jimenez, Elodie-Laure; Sablin, Mikhail; Losey, Robert J. (2017). "Palaeolithic and prehistoric dogs and Pleistocene wolves from Yakutia: Identification of isolated skulls".Journal of Archaeological Science.78:1–19.Bibcode:2017JArSc..78....1G.doi:10.1016/j.jas.2016.11.008.
^Mathieson et al. 2018, p. 52-53 "Supplementary Information page 52: "The derived allele of the KITLG SNP rs12821256 that is associated with – and likely causal for blond hair in Europeans is present in one hunter-gatherer from each of Samara, Motala and Ukraine (I0124, I0014 and I1763), as well as several later individuals with Steppe ancestry. Since the allele is found in populations with EHG but not WHG ancestry, it suggests that its origin is in the Ancient North Eurasian (ANE) population. Consistent with this, we observe that the earliest known individual with the derived allele (supported by two reads) is the ANE individual Afontova Gora 3, which is directly dated to 16130-15749 cal BCE (14710±60 BP, MAMS-27186: a previously unpublished date that we newly report here). We cannot determine the status of rs12821256 in Afontova Gora 2 and MA-1 due to lack of sequence coverage at this SNP.".
^Mathieson et al. 2018 "Supplementary Information page 52: "The derived allele of the KITLG SNP rs12821256 that is associated with – and likely causal for blond hair in Europeans is present in one hunter-gatherer from each of Samara, Motala and Ukraine (I0124, I0014 and I1763), as well as several later individuals with Steppe ancestry. Since the allele is found in populations with EHG but not WHG ancestry, it suggests that its origin is in the Ancient North Eurasian (ANE) population. Consistent with this, we observe that the earliest known individual with the derived allele (supported by two reads) is the ANE individual Afontova Gora 3, which is directly dated to 16130-15749 cal BCE (14710±60 BP, MAMS-27186: a previously unpublished date that we newly report here). We cannot determine the status of rs12821256 in Afontova Gora 2 and MA-1 due to lack of sequence coverage at this SNP."
^abZhang, Fan (November 2021)."The genomic origins of the Bronze Age Tarim Basin mummies".Nature.599 (7884):256–261.Bibcode:2021Natur.599..256Z.doi:10.1038/s41586-021-04052-7.ISSN1476-4687.PMC8580821.PMID34707286.The Tarim mummies are among only a few known Holocene populations that derive the majority of their ancestry from Pleistocene ANE groups, who once made up the huntergatherer populations of southern Siberia, and which are represented by individual genomes from the archaeological sites of Mal'ta (MA-1)29 and Afontova Gora (AG3). (...) The Tarim mummies are currently the best representative of the pre-pastoralist ANE-related population that once inhabited Central Asia and southern Siberia (Extended Data Fig. 2A), even though Tarim_EMBA1 postdates these populations in time.
^"The earliest known example of the classic European blond hair mutation is in an Ancient North Eurasian from the Lake Baikal region of eastern Siberia from seventeen thousand years ago. The hundreds of millions of copies of this mutation in central and western Europe today likely derive from a massive migration of people bearing Ancient North Eurasian ancestry, an event that is related in the next chapter."
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