Tianyuan man
| Tianyuan man | |
|---|---|
| Location | |
Tianyuan man and contemporary cultures c. 50,000~40,000 |
Tianyuan man (simplified Chinese: 田园洞人; traditional Chinese: 田園洞人; pinyin: Tiányuándòng Rén) is the remains of one of the earliest modern humans to inhabit East Asia. In 2007, researchers found 34 bone fragments belonging to a single individual at the Tianyuan Cave near Beijing, China.[1][2] Radiocarbon dating shows the bones to be between 42,000 and 39,000 years old, which may be slightly younger than the only other finds of bones of a similar age at the Niah Caves in Sarawak on the South-east Asian island of Borneo.
Tianyuan man is one of the oldest known members of the East Eurasian lineage that gave rise to (among others) modern East and Southeast Asians, Siberians and Native Americans.
Subsistence
Nothing is known directly about the material culture of this individual, since so far, no artefacts or other cultural remains have been found at the site.[2] Isotope analysis suggests that a substantial part of his diet came from freshwater fish.[3]
Physical anthropology
Morphology
Tianyuan man is considered to be early modern Homo sapiens. He lacks several mandibular features common among late archaic West Eurasian humans, showing his divergence. Based on the rate of dental occlusal attrition, he died in his 40s or 50s.[2] The observed derived modern human features and the high crural index of Tianyuan 1, suggest "some relatively recent ancestry among more equatorial populations".[4]
Like the Zhoukoudian remains from Beijing, the Tianyuan remains retained more "southern" morphological features associated with populations that initially colonized the Asia-Pacific region from the southern route.[5]
Archaeogenetics
The first DNA analysis of the Tianyuan remains (focusing on mtDNA and chromosome 21) was published in 2013 and revealed that Tianyuan man is related "to many present-day Asians and Native Americans" and had already diverged genetically from the ancestors of modern Europeans.[6] He belonged to mitochondrial DNA haplogroup B,[6] and paternal haplogroup K2b.[7]
A genome-wide analysis confirmed the close affinity of Tianyuan man to modern East Asian and Southeast Asian populations as well as other Basal Asians such as the Hoabinhians, Xingyi or Papuan lineages; it was also found that the Tianyuan lineage is not directly ancestral to modern populations, but rather represents a deeply diverged member of the East and Southeast Asian (ESEA) lineage, basal to all later populations of East and Southeast Asia.[8][9][10][11][12] The Tianyuan man was determined to be part of an Initial Upper Paleolithic wave, at least 45,000 years ago, "ascribed to a population movement with uniform genetic features and material culture" (Ancient East Eurasians), and sharing deep ancestry with other ancient specimens such as Bacho Kiro, Peștera cu Oase, the Ust'-Ishim man, as well as the ancestors of modern day Papuans (Australasians).[13] The lineage ancestral to the Tianyuan man (dubbed as the "ESEA" lineage) is inferred to have diverged from the Ancient East Eurasians, following a Southern Route dispersal, and subsequently diverged into the Hoabinhian lineage, the Tianyuan lineage, and a lineage ancestral to all modern East and Southeast Asians.[10]
The Tianyuan lineage can be modeled as a Paleolithic admixture of an Onge-like source from Southeast Asia (c. 61%) and a deeply diverged East Eurasian source associated with the IUP movements into Siberia (c. 39%), which were distantly related to the Bacho Kiro cave remains.[14][11][15][13] An earlier model estimated around 64% ancestry related to Eastern Asians and 36% ancestry represented by the deeply diverged Ust'-Ishim man, who represents an "early leaf on the East Eurasian tree", close to a trifurication between West and East Eurasians.[16][13]
Tianyuan man exhibits unusually high genetic affinities with GoyetQ116-1 from the Goyet Caves in Namur province, Belgium. GoyetQ116-1 shares more alleles with Tianyuan man compared to other contemporary West Eurasian individuals.[8][17] The GoyetQ116-1 specimen is inferred to have 17–23% ancestry from an IUP-affiliated population distantly related to that one which also contributed to the Tianyuan man. This population is closely related to the Bacho Kiro cave remains.[18][14] Villalba-Mouco et al. (2023) argues that this IUP-affiliated population pre-dated the split between European and Asian populations.[19] Another study suggests that the IUP-affiliated population was part of the earliest East Eurasian expansions in Eurasia and eventually, became distinct through additional admixture with archaic humans. [20]
Tianyuan man also displays high genetic affinities with a 33,000-year-old specimen (AR33K), who lived between the Amur region and modern day Mongolia, suggesting that Tianyuan-like ancestry was widespread northeastern Asia during the Paleolithic period. This genetic cluster is also known as "Tianyuan cluster". The Tianyuan cluster was later replaced by Ancient Northern East Asian ancestry during the Last Glacial Maximum (19,000 to 26,000 years ago), evident by the Amur19k remains, although the exact circumstances remain inconclusive. The Amur19k remains were found to be basal to later Northern East Asian remains, and could already be distinguished from Ancient Southern East Asian remains.[22][23][12][11]
The Tianyuan-related cluster lacked the derived variant of the EDAR gene allele, which was observed among the Amur19k individual and succeeding Northern East Asian remains. The allele was also absent from other East Eurasian populations, such as Papuans or the Jōmon people of Japan.[11] A 2025 study states that the Tianyuan Man had the highest Denisovan ancestry among East Eurasians.[24]
Contributions to later populations
Ancient and modern East Asians derive most of their ancestry from an Onge-related population (76–79%), with additional gene flow from a Tianyuan-related population (21–24%). Around 22,000 to 26,000 years ago, the Tianyuan cluster was replaced by East Asian-like ancestry.[11][15][25] According to a 2025 study, ancient East Asians are equally diverged from the Basal Asian Xingyi and Tianyuan lineages, suggesting that the ancestors of ancient East Asians are an admixture of ancestries related to Tianyuan Man and Early Neolithic Xingyi. Although the Hoabinhian, Early Neolithic Xingyi, and Tianyuan lineages are equally diverged from East Asians and each other, the Hoabinhian and Xingyi display some connections to East Asians, possibly due to more recent gene flow.[12][26]
A Tianyuan-like population contributed around 29–50% ancestry to the Ancient North Eurasians, with the remainder being made up by Early West Eurasian ancestry represented by the Kostenki-14 specimen. A c. 34,000 year old specimen from Northern Mongolia (Salkhit) derives approximately 75% ancestry from a Tianyuan-like population, with the remainder (25%) being derived from a Yana-like population. The Salkhit individual displayed a complex bi-directional relationship to the Ancient North Eurasians.[27][18][13] There is also evidence for low amounts (c. 2%) of Tianyuan-related geneflow into the Uppee Paleolithic Sungir population of Western Russia, consistent with traces of Denisovan ancestry.[28] Similarly, GoyetQ116-1 from western Europe shares excess affinity with both Tianyuan and the BachoKiro_IUP specimen although this is due to gene flow from the latter.[29] While increased Tianyuan affinity among Eastern hunter-gatherers is explained by high Ancient North Eurasian ancestry, a similar affinity observed among Iberian hunter-gatherers (MLZ) is instead explained by high GoyetQ116-1 ancestry.[19]
Basal East Asian or "Deep Asian" ancestry, represented by Tianyuan or Andamanese Onge, directly contributed to the peopling of Southeast Asia, following the establishment of deeply diverged Australasian ancestry and preceding Mesolithic and Neolithic expansions of Ancient Southern East Asians associated with the spread of Austroasiatic and Austronesian languages.[21]
The Tianyuan man also shares more alleles with South American populations, such as the Surui and Karitiana in Brazil and Chane in northern Argentina and southern Bolivia, than with other indigenous Americans.[30]
See also
References
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- ^ a b c Shang, Hong (2007). "An early modern human from Tianyuan Cave, Zhoukoukian, China". Proceedings of the National Academy of Sciences. 104 (16): 6573–8. Bibcode:2007PNAS..104.6573S. doi:10.1073/pnas.0702169104. PMC 1871827. PMID 17416672.
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- ^ Shang, Hong; Tong, Haowen; Zhang, Shuangquan; Chen, Fuyou; Trinkaus, Erik (17 April 2007). "An early modern human from Tianyuan Cave, Zhoukoudian, China". Proceedings of the National Academy of Sciences. 104 (16): 6573–6578. Bibcode:2007PNAS..104.6573S. doi:10.1073/pnas.0702169104. PMC 1871827. PMID 17416672.
The high crural indices and tibial robusticity of Tianyuan 1 may well indicate some combination of equatorial ancestry and an emphasis on mobility (37, 38).
- ^ Matsumura, Hirofumi; Hung, Hsiao-chun; Higham, Charles; Zhang, Chi; Yamagata, Mariko; Nguyen, Lan Cuong; Li, Zhen; Fan, Xue-chun; Simanjuntak, Truman; Oktaviana, Adhi Agus; He, Jia-ning; Chen, Chung-yu; Pan, Chien-kuo; He, Gang; Sun, Guo-ping (5 February 2019). "Craniometrics Reveal "Two Layers" of Prehistoric Human Dispersal in Eastern Eurasia". Scientific Reports. 9 (1): 1451. Bibcode:2019NatSR...9.1451M. doi:10.1038/s41598-018-35426-z. ISSN 2045-2322. PMC 6363732. PMID 30723215.
...ancient people perhaps of the "first layer" with Australo-Papuan features moved into Siberia and subsequently adapted to the extremely cold climate during the Last Glacial Maximum (LGM) of 24–16 kya.
- ^ a b Fu, Q.; Meyer, M.; Gao, X.; Stenzel, U.; Burbano, H.A.; Kelso, J.; Pääbo, S. (2013). "DNA analysis of an early modern human from Tianyuan Cave, China". Proceedings of the National Academy of Sciences. 110 (6): 2223–2227. Bibcode:2013PNAS..110.2223F. doi:10.1073/pnas.1221359110. PMC 3568306. PMID 23341637.
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...the ESEA lineage differentiated into at least three distinct ancestries: Tianyuan ancestry which can be found 40,000-33,000 years ago in northern East Asia, ancestry found today across present-day populations of East Asia, Southeast Asia, and Siberia, but whose origins are unknown, and Hòabìnhian ancestry found 8,000-4,000 years ago in Southeast Asia, but whose origins in the Upper Paleolithic are unknown.
- ^ a b c d e Bennett, Andrew E.; Liu, Yichen; Fu, Qiaomei (2025). Reconstructing the Human Population History of East Asia through Ancient Genomics. doi:10.1017/9781009246675. ISBN 978-1-009-24667-5.
The Tianyuan genetic cluster disappears from the record, and not far from where AR33K lived near the Songua River, remains from a 19,000-year-old individual, AR19K, were identified instead to be more closely related to present-day East Asians. AR19K, who was also found without any archeological context, lived at the last years of the LGM when warming temperatures were beginning to return to what was still a cold steppe environment of northern East Asia, yet it is currently unclear when the AR19K-related population first migrated to the area, or when Tianyuan ancestry vanished, and what role the severe climatic and environmental changes of the LGM played in this population replacement. Several statistical models show that AR19K ancestry is basal to younger ancestries found throughout ancient coastal northern East Asia, and also that AR19K clusters more closely to ancient coastal northern East Asia populations than to ancient coastal southern East Asian ancestry (Mao et al. Reference Mao, Zhang and Qiao2021). This prominent genetic distinction between northern and southern East Asian populations had been observed earlier with younger samples (Yang et al. Reference Yang, Fan and Sun2020), but these results indicate that by 19,000 years ago this population structure was already in place.
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Tianyuan and AR33K form a clade with respect to all other Asians, indicating that they are sister groups carrying the same Basal Asian Ancestry, denoted Tianyuan ancestry (1). First, we find that ancient lowland northern and southern East Asians (nEA/sEA) shares genetic connections to both Tianyuan/AR33K and Xingyi_EN, i.e f4(Mbuti, Xingyi_EN; Tianyuan/AR33K, nEA/sEA)>0 (2.2<Z<5.6) and f4(Mbuti, Tianyuan/AR33K; Xingyi_EN, sEA/nEA)≥0 (0.5<Z<4.6, Data S2c). Comparing ancient northern and southern East Asians directly to Xingyi_EN and the Tianyuan/AR33K group shows that most ancient East Asians are similarly related to both, i.e. f4(Mbuti, nEA/sEA; Xingyi_EN, Tianyuan/AR33K)~0 (-2.9<Z<0.5, Data S2c), with the exception of AR14K (-3.5<Z<-1.7), Qihe3 (-3.8<Z<-3.5), and Tanshishan (-4.5<Z<-3.7) potentially indicating a slight connection between some ancient East Asians and Xingyi_EN. Overall, these patterns indicate that Xingyi_EN is not related to individuals carrying Tianyuan ancestry, and Xingyi_EN-related ancestry is as deeply diverged from ancient East Asians as populations carrying Tianyuan ancestry. The patterns may also suggest that the ancestor of ancient East Asians is a mixture of different ancestries related to both of these deeply diverged populations.
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Xingyi_EN-related ancestry is as deeply diverged from ancient East Asians as populations carrying Tianyuan ancestry. The patterns may also suggest that the ancestor of ancient East Asians is a mixture of different ancestries related to both of these deeply diverged populations. ... In the Treemix analysis with 1,000 bootstrap replicates, Tianyuan as outgroup to Xingyi_EN, La368, and all East Asians is strongly supported (97.8%, Fig. 2a, Supplementary Text S6). In the outgroup-f3-analysis, Xingyi_EN shows a slightly higher affiliation with East Asians than Tianyuan and the Hòabìnhian La368 (Fig. 2c). Overall, we find that Tianyuan ancestry, Hòabìnhian ancestry, and ancestry related to Xingyi_EN are generally equidistant to each other, though other analyses (e.g. Treemix and outgroup-f3) show some connections of Xingyi_EN and La368 with recent East Asians.
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