Peopling of China

History of ancient China

A population genomic PCA graph, showing the substructure of East Asian populations, including Han Chinese (2019)[1]

In the course of the peopling of the World by Homo sapiens, East Asia was reached about 50,000 years ago (50 kya). The "recent African origin" lineage of 70 kya diverged into identifiable East Eurasian and West Eurasian lineages by about 50 kya.[2][3] The East Eurasian ancestors of East Asians used a southern route to reach South and Southeast Asia, along which they rapidly diverged into the ancestors of Indigenous South Asians (AASI), Papuans, East Asians and Andamanese peoples (such as the Onge).[4] This early East Asian lineage diverged further during the Last Glacial Maximum, contributing outgoing from Mainland Southeast Asia significantly to the peopling of the Americas via Beringia about 25 kya.[5] After the last ice age China became cut off from neighboring island groups. The previous phenotypes of early East Asians became either replaced or prevailed among more geographically distant groups.[6][7]

## Genetic history

[edit]

Further information: Han Chinese § DNA and genetics analysis, Mongoloid, and Proto-Mongoloid

### Overview

[edit]

A "Basal-East Asian population" referred to as the East- and Southeast Asian lineage (ESEA); is ancestral to modern East Asians, Southeast Asians, Polynesians, and Siberians, but also ancestral to the Hoabinhian hunter-gatherers of Southeast Asia and the ~40,000 year old Tianyuan lineage found in Northern China. The ESEA lineage descend from an earlier "eastern non-African" (ENA) or "Ancient East Eurasian" meta-population, which used a single southern route to reach South, Southeast Asia, and Oceania, and along which they rapidly diverged into the ancestors of Ancient South Asians (AASI), East/Southeast Asians (ESEA), as well as Australasians. The early ESEA lineage is inferred to have than diverged into the Hoabinhian, the Tianyuan, and Ancient East Asian lineages, and expanded northward. There is "a strong correlation with latitude, with diversity decreasing from south to north".[8][4]

### Genetic studies of Shaanxi and Liaoning

[edit]

One study showed some Han Chinese individuals in Shaanxi carry maternal haplogroup U.[9] Other mtDNAs that some Han Chinese have are W6 and H. Some Han Chinese also carried paternal haplogroup R1a1.[10]

Several studies reveal minor West Eurasian-derived admixture among Shaanxi Han Chinese, especially those living in Guanzhong and Shaanbei (2–5%),[10][11] and Liaoning Chinese (~2%).[12] Ancient North Eurasian admixture is more dominant among Shaanxi Han Chinese compared to other Han subgroups.[10]

### Archaeogenetic studies in Guangxi

[edit]

Wang et al. (2021) found that the ancestries of individuals in Guangxi from between 9,000–6,000 BP can be modeled as mixtures of Upper Paleolithic source populations from both Guangxi and Fujian. During the early and late Neolithic, migration of Austronesians from the Fujian region's Neolithic Austronesians significantly influenced the genetic profile of the Guangxi region but did not completely replace the earlier resident hunter-gatherer ancestry that was local to Guangxi. Neolithic Fujian is genetically unrelated to Modern Fujian. The main archaic individuals that were analyzed include the following.[13]

* Archaic individuals from 12,000–10,000 BP
* Longlin (隆林) (10,686–10,439 cal BP; Laomocao Cave 老磨槽洞, Longlin Autonomous County, Guangxi, China) is an Upper Paleolithic individual that was found to carry deep diverging East Asian ancestry. Even though the Longlin remains were found to have some physical features resembling those of archaic humans, genetic analysis revealed that Longlin carried similar levels of archaic human ancestry as in Neolithic and present-day East Asians. Longlin appears to be closely related to the Maludong or Red Deer Cave people. Genetic analysis also indicated that Longlin is more closely related to Ikawazu (ca. 2,700 BP; Ikawazu Shell Midden site (伊川津貝塚), Atsumi Peninsula, southern Aichi Prefecture, central Honshu, Japan), a Jomon individual, than to basal Asian lineages such as Hoabinhian. Longlin, Ikawazu, and coastal Neolithic East Asians from Shandong and Fujian likely all diverged from each other at around the same time.
* Qihe-3 (奇和) (11,747–11,356 cal BP; Qihe Cave 奇和洞, Zhangping, Fujian) is an Upper Paleolithic individual from the mountainous interior of Fujian, located about 100 km north of present-day Zhangzhou city. Qihe-2, a more recent specimen from a different layer of the same site dating to 8,428-8,359 cal BP, was also sequenced and found to be closely related to Iron Age Taiwanese and present-day Austronesians. Qihe-3 can be modeled as a mixture of ancestry found in coastal Neolithic East Asians (e.g., Boshan in Neolithic Shandong and Liangdao in Neolithic Fujian), as well as another deeply diverging East Asian lineage. A later specimen, Liangdao-2 (~7,600 BP; Liangdao, Fujian),[14] was found to have mostly Qihe-3-related ancestry (82%–90%), as well as a smaller percentage of northern East Asian ancestry (10%–18%) that can be associated with Neolithic Shandong and other northern East Asian sites. As a result, there is more genetic continuity from the early to late Neolithic in Fujian than there is in Guangxi.
* Archaic individuals from 9,000–6,000 BP
* Dushan (独山) (8,974–8,593 cal BP; Linfeng Town 林逢镇, Tiandong County, Guangxi) is a male individual that can be modeled as a mixture of Longlin-related ancestry (17%) and Prehistoric Fujian Austronesian-related ancestry (Qihe, 83%).
* Baojianshan (宝剑山) (8,335–6,400 cal BP; Baojianshan Cave site (Baojianshan Cave A), Longzhou County, Chongzuo City, Guangxi) can be modeled as a mixture of 72.3% Dushan-related ancestry and 27.7% Hoabinhian-related ancestry.

Huang et al. (2022) associate Dushan and Baojianshan-related ancestry with the first Neolithic farmers in Mainland Southeast Asia (MSEA), i.e. late Neolithic farmers who expanded from southern China into MSEA. Among present-day populations, they found that:[15]

* Khmuic (Austroasiatic) speakers in Mainland Southeast Asia, such as the Mal (Htin) and Mlabri, mostly carry first MSEA farmer-related ancestry (69.2–75.2%).
* West Hmongic speakers (Longlin Miao, Xilin Miao, and Hmong) have slightly more first MSEA farmer-related ancestry (32.3–35.0%) than Neolithic Fujian Austronesian-related ancestry (23.7–26.0%).
* Hlai, Maonan, and Guangxi Zhuang were found to have more Neolithic Fujian Austronesian-related ancestry (40.7–53.9%, with Hlai carrying the most at 46.1–53.9%) than first MSEA farmer-related ancestry (24.9–33.1%).
* Similar to Kra-Dai-speaking populations, Southern Han Chinese in Fujian and Guangdong carry more late Neolithic Fujian Austronesian-related ancestry (35.0–40.3%) than first MSEA farmer-related ancestry (21.8–23.6%).

Guangxi region individuals from 1,500–500 BP show genetic profiles that can be identified with present-day Kra-Dai and Hmong-Mien-speaking populations of southern China. They can be modeled as a mixture of 58.2%–90.6% Dushan-related (or Qihe-3-related) ancestry and 9.4%–41.8% northern East Asian-related ancestry, with the later attributed to relatively recent historical migrations from the north.[15]

### Paternal lineages

[edit]

A PCA graph illustrating the genetic makeup of Han Chinese and other Asian populations.[16] Hypothetical migration patterns of paternal human lineages Haplogroup O, also known as O-M175, is primarily found among populations in Southeast Asia and China.

Looking at Y-DNA studies, it would seem that East Asian paternal lineages expanded in Asia approximately 50,000 years ago. People bearing genetic markers ancestral such as C, D, N, and O, as well as P (specifically Q), came through the Himalayan mountain range and proceeded to Southeast Asia.[17][18] Haplogroup C moved to East Asia and Australia, with at least two subclades of the major East Asian branch migrating into the Americas, and with members of Haplogroup C-M38 spreading throughout Wallacea, New Guinea, Melanesia, and Polynesia. Another group of peoples, bearing the Y-DNA Haplogroup D, has left descendants mostly in the Andaman Islands, Tibet, and Japan.[19][20] Haplogroup Q, believed to have arisen in Central Asia or Southern Siberia approximately 17,000 to 22,000 years ago, went north to populate Northern Siberia and the Americas. Some northern Chinese have this genetic marker. Haplogroups N and O, originated in Southern China and by 10,000 years ago went on to populate first Southeast Asia and then from Southeast Asia, left for East Asia. Roughly 12,000 years ago, during the Neolithic period, farmers settled along the Yellow River. Alongside various other lineages including O2‐M122, they initiated the development of agriculture. About 6000 years ago, ancestors of the Tibetans split off from this parent group. About 5,000 years ago, Neolithic Yellow River farmers experienced rapid expansion, with notable gene flow into surrounding populations.[21] This corresponds to the late period (2600-2000 BC) of the Longshan culture in the middle Yellow River area. As the Neolithic population in China reached its peak, the number of settlements increased. In some locations, such as the basin of the Fen River in southern Shanxi, the Yellow River in western Henan (confined by the Zhongtiao Mountains and Xiao Mountains), and the coastal Rizhao plain of southeast Shandong, a few very large (over 200 ha) centers developed. In more open areas, such as the rest of Shandong, the Central Plain (in Henan) and the Wei River basin in Shaanxi, local centers were more numerous, smaller (generally 20 to 60 ha) and fairly evenly spaced. Walls of rammed earth have been found in 20 towns in Shandong, nine in the Central Plain, and one (Taosi) in southern Shanxi, suggesting conflict between polities in these areas.

The expansion and rise of these various settlements could be due to the impetus of the collective benefit of the construction of irrigation works in the late Neolithic:

"Most of the labor to dike and drain an area is associated with digging a ditch and sidecasting the soil to make an earthen dike. To make the culvert and tide gate you can use an old worn-out canoe for the pipe .... and use just about any good-sized flat stones you can get your hands on. If you have twice as many people making your dike, you can make twice as many linear feet of dike. Doubling the perimeter of a square dike results in quadrupling the area within the dike."

The agricultural surplus would have allowed for a rapidly expanding population, which would provide more labor for irrigation. By the time of the establishment of the Xia and Shang dynasties, population estimates were at approximately 13 million people.[22]

Studies of DNA remnants from the Central Plains area of China 3000 years ago show close affinity between that population and those of Northern Han today in both the Y-DNA and mtDNA. Both northern and southern Han show similar Y-DNA genetic structure.[23]

Y-chromosome haplogroup O2-M122 is a common DNA marker in Han Chinese, as it appeared in China in prehistoric times. It is found in more than 50% of Chinese males, with frequencies tending to be high toward the east of the country (30/101 = 29.7% Guangxi Pinghua Han,[24] 13/40 = 32.5% Guangdong Han,[25] 11/30 = 36.7% Lanzhou Han,[26] 26/60 = 43.3% Yunnan Han,[27] 251/565 = 44.4% Zhaotong Han,[28] 15/32 = 46.9% Yili Han,[26] 23/49 = 46.9% Lanzhou Han,[29][30] 32/65 = 49.2% South China Han,[31] 18/35 = 51.4% Meixian Han,[26] 22/42 = 52.4% Northern Han,[32] 43/82 = 52.4% Northern Han,[33] 18/34 = 52.9% Chengdu Han,[26] 154/280 = 55.0% Southern Han,[33] 27/49 = 55.1% Northern Han,[34] 73/129 = 56.6% North China Han,[31] 49/84 = 58.3% Taiwan Han,[25] 35/60 = 58.3% Taiwan Minnan,[35] 99/167 = 59.3% East China Han,[31] 33/55 = 60.0% Fujian Han,[35] 157/258 = 60.9% Taiwan Han,[35] 13/21 = 61.9% Taiwan Han,[34] 189/305 = 62.0% Zibo Han,[28] 23/35 = 65.7% Harbin Han,[26] 29/44 = 65.9% Northern Han,[25] 23/34 = 67.6% Taiwan Hakka,[35] 35/51 = 68.6% Beijing Han[27]).[36][37]

During the Zhou dynasty, or earlier, peoples with haplogroup Q-M120 likewise also contributed to the ethnogenesis of Han Chinese people. This haplogroup is implied to be widespread in the Eurasian steppe and north Asia since it is found among Cimmerians in Moldova and Bronze Age natives of Khövsgöl. But it is currently near-absent in these regions except for East Asia. In modern China, haplogroup Q-M120 can be found in the northern and eastern regions.[38]

Han Chinese are genetically distinguishable from Yamato Japanese and Koreans, and internally the different Han Chinese subgroups are genetically closer to each other than any of them are to Koreans and Japanese. However, some Southern Han Chinese, such as Guangxi Han, are genetically closer to Vietnamese and Dai people than Northern Han. But meanwhile, when compared to Europeans genetics, the Han Chinese, Southeast Asian, Japanese and Koreans are closer to each other than Europeans and South Asians. Genealogical research has indicated extremely similar genetic profiles of a less than 1% total variation in spectrum between these three groups.[39] Some Southern Han Chinese and Northern Han Chinese are closest to each other and show the smallest differences when they are compared to other Asians. Vietnamese Ho Chi Minh City Kinh are close to Xishuangbanna's Dai ethnic minority and Guangdong Han Chinese.[40] Koreans are also relatively close to northern Han Chinese. Japanese are more genetically distant from Koreans than Koreans are from northern Han Chinese. However Buryat Mongols and Qinghai Mongols are further from each other than Japanese and Korean despite both being Mongols.[41] Comparisons between the Y chromosome SNP and MtDNA of modern Northern Han Chinese and 3,000 year old Hengbei ancient samples from China's Central Plains show they are extremely similar to each other and show continuity between ancient Chinese of Hengbei and current Northern Han Chinese while Southern Han Chinese were different from the people of Hengbei. This showed that already 3,000 years ago the current northern Han Chinese genetic structure was already formed.[23]

### Maternal lineages

[edit]

The mitochondrial-DNA haplogroups of the Han Chinese can be classified into the northern East Asian-dominating haplogroups, including A, C, D, G, M8, M9, and Z, and the southern East Asian-dominating haplogroups, including B, F, M7, N*, and R.[42]

These haplogroups account for 52.7% and 33.85% of those in the Northern Han, respectively.

Haplogroup mtDNA D descend from Dravidian Haplogroup M mtdna is the modal mtDNA haplogroup among northern East Asians. Among these haplogroups, D, B, F, and A were predominant in the Northern Han, with frequencies of 25.77%, 11.54%, 11.54%, and 8.08%, respectively.

However, in the Southern Han, the northern and southern East Asian-dominating mtDNA haplogroups accounted for 35.62% and 51.91%, respectively. The frequencies of haplogroups D, B, F, and A reached 15.68%, 20.85%, 16.29%, and 5.63%, respectively.[43][44][45][46][47]

## Climate history

[edit]

During the Last Glacial Maximum, 29,000 to 18,000 years ago, northern China was a treeless steppe with areas of permafrost and southern China lost much of its forest cover. The sea level was much lower. Borneo, Indonesia, the Philippines, and the Japanese archipelago may have been accessible by land. With the end of the last ice age, a period of warming occurred lasting from 18,000 to 10,000 years ago. The oceans rose and inundated vast regions leaving little trace of coastal settlements used by these people. We know little about their languages. Their cultures are likely to have been diverse. There are many limestone cave sites in southern China which show human settlements. There is evidence of pottery making. The inhabitants had bone tools, fished, and hunted pigs and deer.[48]

It is believed that the climate in southern China was warmer and wetter south of the Qinling mountains; elephants are known to have inhabited the Yangtze river region. The climate in Northeast China north of present-day Beijing was characterized as a cold steppe environment during this period. The presence of woolly mammoth is well documented.[49]

The climate was also much warmer between 8,000 and 3,500 years ago. In the Shandong region, excavations have found the bones of alligators and elephants.

The development of agriculture about 10,000 years ago, with the domestication of millet in the Yellow River valley region and rice in the Yangtze River valley, may have been associated with accelerated growth in the number and size of settlements and the intensified development of local cultures and languages.[50]

## Settlement patterns

[edit]

Early settlements in the Chinese Upper Paleolithic were either hunter-gatherer societies, or marine environment based societies characterized by shell middens.[51] Relatively speaking the land was sparsely populated, as the peoples followed the coastal regions and the river valleys.

Neolithic settlements have been found from Liaoning province in the northeast to the Chengdu region in the southwest; from Gansu province in the northwest to sites in Fujian in the southeast. The settlement pattern in the Tibetan region is still unclear as there is debate as to whether there was a pre-Neolithic population movement into the region.[52]

## Holocene China

[edit]

Further information: History of China

The origin of Sino-Tibetan is uncertain. It dates to the Neolithic, or just before the Neolithic. There are various proposals. Van Driem (2005) proposes that Sino-Tibetan originated in the Sichuan Basin before 7000 BC, with an early migration into northeast India, and a later migration north of the predecessors of Chinese and Tibetic.[citation needed] Matisoff (1991) places its origins in the eastern part of the Tibetan plateau around 4000 BC, with the various groups migrating out along the Yellow, Yangtze, Mekong, Salween and Brahmaputra rivers.[citation needed] Blench and Post (2014) have proposed that the Sino-Tibetan homeland was in northeast India, the area of greatest diversity, around 7000 BC.[citation needed] Blench (2009) proposes that the earliest speakers of Sino-Tibetan were not farmers, since agriculture cannot be reconstructed for Proto-Sino-Tibetan. Rather, early Sino-Tibetan speakers were highly diverse hunter-gatherers and foragers.[53] More recent study published in the Proceedings of the National Academy of Sciences of the United States of America point to the origin of the Sino-Tibetan in northern China in the Neolithic Cishan culture and Yangshao culture.[54]

The Austroasiatic languages (including Vietnamese, Khmer, etc.) likely originated from Southern China and would have entered Southeast Asia via Yunnan and the Mekong. Likewise, the Miao, Thai, Burmese, and Tibetan languages evolved in China. It is even accepted that proto-Austronesian speakers originated from China, migrated to Taiwan (Formosa), and then to the islands of the Pacific, especially since Taiwan is the place exhibiting the most diversity in Austronesian languages (see Formosan languages). By 3,000 years ago, the sophistication of some of the cultures neighboring that of the Han Chinese can be seen in the bronze artifacts of the Sanxingdui (Sichuan), Ban Chiang (Thailand) and Dong Son (Vietnam). The domestication of the horse 6,000 years ago in the Eurasian steppes led to cultures that mixed animal husbandry and agriculture. Indo-European speakers are known to have reached the Xinjiang region 4,000 years ago (see Tocharians).

Because the East Asian landmass was initially populated from the south, and the historical record shows the Han Chinese migrating to the south and southwest, the genetic relationship among all the peoples of China remains a challenging study.[55]

## See also

[edit]

* Peopling of Southeast Asia
* List of Paleolithic sites in China
* List of Neolithic sites in China
* List of Bronze Age sites in China
* List of first human settlements
* Han Chinese § DNA and genetics analysis[broken anchor][broken anchor][broken anchor]

## References

[edit]

1. ^ Huang, Xiufeng; Xia, Zi-Yang; Bin, Xiaoyun; He, Guanglin; Guo, Jianxin; Adnan, Atif; Yin, Lianfei; Huang, Youyi; Zhao, Jing; Yang, Yidong; Ma, Fuwei; Li, Yingxiang; Hu, Rong; Yang, Tianle; Wei, Lan-Hai; Wang, Chuan-Chao (30 June 2022). "Genomic Insights Into the Demographic History of the Southern Chinese". Frontiers in Ecology and Evolution. 10. doi:10.3389/fevo.2022.853391.
2. ^ Seguin-Orlando, Andaine; Korneliussen, Thorfinn S.; Sikora, Martin; Malaspinas, Anna-Sapfo; Manica, Andrea; Moltke, Ida; Albrechtsen, Anders; Ko, Amy; Margaryan, Ashot; Moiseyev, Vyacheslav; Goebel, Ted; Westaway, Michael; Lambert, David; Khartanovich, Valeri; Wall, Jeffrey D.; Nigst, Philip R.; Foley, Robert A.; Lahr, Marta Mirazon; Nielsen, Rasmus; Orlando, Ludovic; Willerslev, Eske (28 November 2014). "Genomic structure in Europeans dating back at least 36,200 years". Science. 346 (6213): 1113–1118. Bibcode:2014Sci...346.1113S. doi:10.1126/science.aaa0114. PMID 25378462. S2CID 206632421.
3. ^ Vallini, Leonardo; Zampieri, Carlo; Shoaee, Mohamed Javad; Bortolini, Eugenio; Marciani, Giulia; Aneli, Serena; Pievani, Telmo; Benazzi, Stefano; Barausse, Alberto; Mezzavilla, Massimo; Petraglia, Michael D.; Pagani, Luca (25 March 2024). "The Persian plateau served as hub for Homo sapiens after the main out of Africa dispersal". Nature Communications. 15 (1): 1882. Bibcode:2024NatCo..15.1882V. doi:10.1038/s41467-024-46161-7. PMC 10963722. PMID 38528002.
4. ^ a b Aoki, Kenichi; Takahata, Naoyuki; Oota, Hiroki; Wakano, Joe Yuichiro; Feldman, Marcus W. (30 August 2023). "Infectious diseases may have arrested the southward advance of microblades in Upper Palaeolithic East Asia". Proceedings of the Royal Society B: Biological Sciences. 290 (2005). doi:10.1098/rspb.2023.1262. PMC 10465978. PMID 37644833. "A single major migration of modern humans into the continents of Asia and Sahul was strongly supported by earlier studies using mitochondrial DNA, the non-recombining portion of Y chromosomes, and autosomal SNP data [42–45]. Ancestral Ancient South Indians with no West Eurasian relatedness, East Asians, Onge (Andamanese hunter–gatherers) and Papuans all derive in a short evolutionary time from the eastward dispersal of an out-of-Africa population [46,47]. [...] The HUGO (Human Genome Organization) Pan-Asian SNP consortium [44] investigated haplotype diversity within present-day Asian populations and found a strong correlation with latitude, with diversity decreasing from south to north. The correlation continues to hold when only mainland Southeast Asian and East Asian populations are considered, and is perhaps attributable to a serial founder effect [50]. These observations are consistent with the view that soon after the single eastward migration of modern humans, East Asians diverged in southern East Asia and dispersed northward across the continent."
5. ^ Moreno-Mayar, J. Víctor; Potter, Ben A.; Vinner, Lasse; Steinrücken, Matthias; Rasmussen, Simon; Terhorst, Jonathan; Kamm, John A.; Albrechtsen, Anders; Malaspinas, Anna-Sapfo; Sikora, Martin; Reuther, Joshua D.; Irish, Joel D.; Malhi, Ripan S.; Orlando, Ludovic; Song, Yun S.; Nielsen, Rasmus; Meltzer, David J.; Willerslev, Eske (2018), "Terminal Pleistocene Alaskan genome reveals first founding population of Native Americans" (PDF), Nature, 553 (7687): 203–207, Bibcode:2018Natur.553..203M, doi:10.1038/nature25173, PMID 29323294, S2CID 4454580
6. ^ Yang, Melinda A. (2022-01-06). "A genetic history of migration, diversification, and admixture in Asia". Human Population Genetics and Genomics. 2 (1): 1–32. doi:10.47248/hpgg2202010001. ISSN 2770-5005.
7. ^ Adhikari, Kaustubh; Fuentes-Guajardo, Macarena; Quinto-Sánchez, Mirsha; Mendoza-Revilla, Javier; Camilo Chacón-Duque, Juan; Acuña-Alonzo, Victor; Jaramillo, Claudia; Arias, William; Lozano, Rodrigo Barquera; Pérez, Gastón Macín; Gómez-Valdés, Jorge; Villamil-Ramírez, Hugo; Hunemeier, Tábita; Ramallo, Virginia; Silva de Cerqueira, Caio C. (2016-05-19). "A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation". Nature Communications. 7 (1): 11616. Bibcode:2016NatCo...711616A. doi:10.1038/ncomms11616. ISSN 2041-1723. PMC 4874031. PMID 27193062.
8. ^ Yang, Melinda A. (2022-01-06). "A genetic history of migration, diversification, and admixture in Asia". Human Population Genetics and Genomics. 2 (1): 1–32. doi:10.47248/hpgg2202010001. ISSN 2770-5005. "...In contrast, mainland East and Southeast Asians and other Pacific islanders (e.g., Austronesian speakers) are closely related to each other [9,15,16] and here denoted as belonging to an East and Southeast Asian (ESEA) lineage (Box 2). …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."
9. ^ https://www.researchgate.net/publication/346962622_Fine-scale_north-to-south_genetic_admixture_profile_in_Shaanxi_Han_Chinese_revealed_by_genome-wide_demographic_history_reconstruction [bare URL]
10. ^ a b c He, Guang-Lin; Wang, Meng-Ge; Li, Ying-Xiang; et al. (2022). "Fine-scale north-to-south genetic admixture profile in Shaanxi Han Chinese revealed by genome-wide demographic history reconstruction". Journal of Systematics and Evolution. 60 (4): 955–972. doi:10.1111/jse.12715 - via Wiley Online Library.
11. ^ Chiang, Charleston W.K.; Mangul, Serghei; Robles, Christopher; Sankararaman, Sriram (2018). "A Comprehensive Map of Genetic Variation in the World's Largest Ethnic Group —Han Chinese". Molecular Biology and Evolution. 35 (11): 2736–2750. doi:10.1093/molbev/msy170. PMC 6693441. PMID 30169787.
12. ^ Zhou, Jingbin; Zhang, Xianpeng; Li, Xin; et al. (2022). "Genetic structure and demographic history of Northern Han people in Liaoning Province inferred from genome-wide array data". Frontiers in Ecology and Evolution. 10. doi:10.3389/fevo.2022.1014024.
13. ^ Wang, Tianyi; Wang, Wei; Xie, Guangmao; Li, Zhen; Fan, Xuechun (2021). "Human population history at the crossroads of East and Southeast Asia since 11,000 years ago". Cell. 184 (14). Elsevier BV: 3829–3841.e21. doi:10.1016/j.cell.2021.05.018. ISSN 0092-8674. PMID 34171307.
14. ^ Wang, Chuan-Chao; Yeh, Hui-Yuan; Popov, Alexander N.; Zhang, Hu-Qin; Matsumura, Hirofumi (2021-02-22). "Genomic insights into the formation of human populations in East Asia". Nature. 591 (7850). Springer: 413–419. Bibcode:2021Natur.591..413W. doi:10.1038/s41586-021-03336-2. ISSN 0028-0836. PMC 7993749. PMID 33618348.
15. ^ a b Huang, Xiufeng; Xia, Zi-Yang; Bin, Xiaoyun; He, Guanglin; Guo, Jianxin (2022-06-30). "Genomic Insights Into the Demographic History of the Southern Chinese". Frontiers in Ecology and Evolution. 10. Frontiers Media SA. doi:10.3389/fevo.2022.853391. ISSN 2296-701X.
16. ^ Soares, Pedro A.; Trejaut, Jean A.; Rito, Teresa; Cavadas, Bruno; Hill, Catherine; Eng, Ken Khong; Mormina, Maru; Brandão, Andreia; Fraser, Ross M.; Wang, Tse-Yi; Loo, Jun-Hun; Snell, Christopher; Ko, Tsang-Ming; Amorim, António; Pala, Maria; MacAulay, Vincent; Bulbeck, David; Wilson, James F.; Gusmão, Leonor; Pereira, Luísa; Oppenheimer, Stephen; Lin, Marie; Richards, Martin B. (2016). "Resolving the ancestry of Austronesian-speaking populations". Human Genetics. 135 (3): 309–326. doi:10.1007/s00439-015-1620-z. PMC 4757630. PMID 26781090.
17. ^ Hallast, Pille; Agdzhoyan, Anastasia; Balanovsky, Oleg; Xue, Yali; Tyler-Smith, Chris (2021-02-01). "A Southeast Asian origin for present-day non-African human Y chromosomes". Human Genetics. 140 (2): 299–307. doi:10.1007/s00439-020-02204-9. ISSN 1432-1203. PMC 7864842. PMID 32666166.
18. ^ Bae, Christopher J.; Douka, Katerina; Petraglia, Michael D. (2017-12-08). "On the origin of modern humans: Asian perspectives". Science. 358 (6368): eaai9067. doi:10.1126/science.aai9067. ISSN 0036-8075. PMID 29217544. S2CID 4436271.
19. ^ "Asian Ancestry based on Studies of Y-DNA Variation: Part 1 Early origins — roots from Africa and emergence in East Asia". Genebase Tutorials. Archived from the original on 2012-01-02. Retrieved 2011-12-28.
20. ^ Shi H, Zhong H, Peng Y, et al. (2008). "Y chromosome evidence of earliest modern human settlement in East Asia and multiple origins of Tibetan and Japanese populations". BMC Biol. 6: 45. doi:10.1186/1741-7007-6-45. PMC 2605740. PMID 18959782.
21. ^ WANG, Chuan-Chao; YAN, Shi; QIN, Zhen-Dong; LU, Yan; DING, Qi-Liang; WEI, Lan-Hai; LI, Shi-Lin; YANG, Ya-Jun; JIN, Li; LI, Hui (May 2013). "Late Neolithic expansion of ancient Chinese revealed by Y chromosome haplogroup O3a1c-002611". Journal of Systematics and Evolution. 51 (3): 280–286. doi:10.1111/j.1759-6831.2012.00244.x. S2CID 55081530.
22. ^ https://docslide.net/documents/relocation-of-civilization-centers-in-ancient-china-environmental-factors.html| "Relocation of Civilization Centers in Ancient China: Environmental Factors"
23. ^ a b Zhao, Yong-Bin; Zhang, Ye; Zhang, Quan-Chao; Li, Hong-Jie; Cui, Ying-Qiu; Xu, Zhi; Jin, Li; Zhou, Hui; Zhu, Hong (4 May 2015). "Ancient DNA Reveals That the Genetic Structure of the Northern Han Chinese Was Shaped Prior to 3,000 Years Ago". PLOS ONE. 10 (5): e0125676. Bibcode:2015PLoSO..1025676Z. doi:10.1371/journal.pone.0125676. PMC 4418768. PMID 25938511.
24. ^ Gan RJ, Pan SL, Mustavich LF, Qin ZD, Cai XY, Qian J, Liu CW, Peng JH, Li SL, Xu JS, Jin L, Li H (2008). "Pinghua population as an exception of Han Chinese's coherent genetic structure". Journal of Human Genetics. 53 (4): 303–13. doi:10.1007/s10038-008-0250-x. PMID 18270655.
25. ^ a b c Hammer MF, Karafet TM, Park H, Omoto K, Harihara S, Stoneking M, Horai S (2006). "Dual origins of the Japanese: common ground for hunter-gatherer and farmer Y chromosomes". Journal of Human Genetics. 51 (1): 47–58. doi:10.1007/s10038-005-0322-0. PMID 16328082.
26. ^ a b c d e Xue Y, Zerjal T, Bao W, Zhu S, Shu Q, Xu J, Du R, Fu S, Li P, Hurles ME, Yang H, Tyler-Smith C (April 2006). "Male demography in East Asia: a north-south contrast in human population expansion times". Genetics. 172 (4): 2431–9. doi:10.1534/genetics.105.054270. PMC 1456369. PMID 16489223.
27. ^ a b Kim SH, Kim KC, Shin DJ, Jin HJ, Kwak KD, Han MS, Song JM, Kim W, Kim W (April 2011). "High frequencies of Y-chromosome haplogroup O2b-SRY465 lineages in Korea: a genetic perspective on the peopling of Korea". Investigative Genetics. 2 (1): 10. doi:10.1186/2041-2223-2-10. PMC 3087676. PMID 21463511. Text was copied from this source, which is available under a Creative Commons Attribution 2.0 (CC BY 2.0) license.
28. ^ a b Yin C, Su K, He Z, Zhai D, Guo K, Chen X, Jin L, Li S (July 2020). "Genetic Reconstruction and Forensic Analysis of Chinese Shandong and Yunnan Han Populations by Co-Analyzing Y Chromosomal STRs and SNPs". Genes. 11 (7): 743. doi:10.3390/genes11070743. PMC 7397191. PMID 32635262.
29. ^ Yao, H., Wang, M., Zou, X. et al., "New insights into the fine-scale history of western–eastern admixture of the northwestern Chinese population in the Hexi Corridor via genome-wide genetic legacy." Mol Genet Genomics 296, 631–651 (2021). https://doi.org/10.1007/s00438-021-01767-0
30. ^ Yao H, Wang M, Zou X, Li Y, Yang X, Li A, Yeh HY, Wang P, Wang Z, Bai J, Guo J, Chen J, Ding X, Zhang Y, Lin B, Wang CC, He G (May 2021). "New insights into the fine-scale history of western-eastern admixture of the northwestern Chinese population in the Hexi Corridor via genome-wide genetic legacy". Molecular Genetics and Genomics. 296 (3): 631–651. doi:10.1007/s00438-021-01767-0. PMID 33650010. S2CID 232091731.
31. ^ a b c Yan S, Wang CC, Li H, Li SL, Jin L (September 2011). "An updated tree of Y-chromosome Haplogroup O and revised phylogenetic positions of mutations P164 and PK4". European Journal of Human Genetics. 19 (9): 1013–5. doi:10.1038/ejhg.2011.64. PMC 3179364. PMID 21505448.
32. ^ Katoh T, Munkhbat B, Tounai K, Mano S, Ando H, Oyungerel G, et al. (February 2005). "Genetic features of Mongolian ethnic groups revealed by Y-chromosomal analysis". Gene. 346: 63–70. doi:10.1016/j.gene.2004.10.023. PMID 15716011.
33. ^ a b Su B, Xiao J, Underhill P, Deka R, Zhang W, Akey J, Huang W, Shen D, Lu D, Luo J, Chu J, Tan J, Shen P, Davis R, Cavalli-Sforza L, Chakraborty R, Xiong M, Du R, Oefner P, Chen Z, Jin L (December 1999). "Y-Chromosome evidence for a northward migration of modern humans into Eastern Asia during the last Ice Age". American Journal of Human Genetics. 65 (6): 1718–24. doi:10.1086/302680. PMC 1288383. PMID 10577926.
34. ^ a b Tajima A, Hayami M, Tokunaga K, Juji T, Matsuo M, Marzuki S, Omoto K, Horai S (2004). "Genetic origins of the Ainu inferred from combined DNA analyses of maternal and paternal lineages". Journal of Human Genetics. 49 (4): 187–93. doi:10.1007/s10038-004-0131-x. PMID 14997363.
35. ^ a b c d Trejaut JA, Poloni ES, Yen JC, Lai YH, Loo JH, Lee CL, He CL, Lin M (June 2014). "Taiwan Y-chromosomal DNA variation and its relationship with Island Southeast Asia". BMC Genetics. 15: 77. doi:10.1186/1471-2156-15-77. PMC 4083334. PMID 24965575.
36. ^ Yan S, Wang CC, Zheng HX, Wang W, Qin ZD, Wei LH, et al. (2014). "Y chromosomes of 40% Chinese descend from three Neolithic super-grandfathers". PLOS ONE. 9 (8): e105691. arXiv:1310.3897. Bibcode:2014PLoSO...9j5691Y. doi:10.1371/journal.pone.0105691. PMC 4149484. PMID 25170956.
37. ^ Hurles ME, Sykes BC, Jobling MA, Forster P (May 2005). "The dual origin of the Malagasy in Island Southeast Asia and East Africa: evidence from maternal and paternal lineages". American Journal of Human Genetics. 76 (5): 894–901. doi:10.1086/430051. PMC 1199379. PMID 15793703.
38. ^ Sun, Na; Ma, Peng-Cheng; Yan, Shi; et al. (2019). "Phylogeography of Y-chromosome haplogroup Q1a1a-M120, a paternal lineage connecting populations in Siberia and East Asia". Annals of Human Biology. 46 (3): 261–266. doi:10.1080/03014460.2019.1632930. PMID 31208219 - via Taylor & Francis Online.
39. ^ Wang, Yuchen; Lu, Dongsheng; Chung, Yeun-Jun; Xu, Shuhua (2018-04-06). "Genetic structure, divergence and admixture of Han Chinese, Japanese and Korean populations". Hereditas. 155 (1): 19. doi:10.1186/s41065-018-0057-5. ISSN 1601-5223. PMC 5889524. PMID 29636655.
40. ^ Yanan Cao; Lin Li; Min Xu; Zhimin Feng; Xiaohui Sun; Jieli Lu; Yu Xu; Peina Du; Tiange Wang; Ruying Hu; Zhen Ye; Lixin Shi; Xulei Tang; Li Yan (30 April 2020). "The ChinaMAP analytics of deep whole genome sequences in 10,588 individuals". Cell Research. 30 (9): 717–731. doi:10.1038/s41422-020-0322-9. PMID 32355288.
41. ^ Wang, Yuchen; Lu, Dongsheng; Chung, Yeun-Jun; Xu, Shuhua (6 April 2018). "Genetic structure, divergence and admixture of Han Chinese, Japanese and Korean populations". Hereditas. 155 (19): 19. doi:10.1186/s41065-018-0057-5. PMC 5889524. PMID 29636655.
42. ^ Wen B, Li H, Lu D, Song X, Zhang F, He Y, et al. (September 2004). "Genetic evidence supports demic diffusion of Han culture". Nature. 431 (7006): 302–305. Bibcode:2004Natur.431..302W. doi:10.1038/nature02878. PMID 15372031. S2CID 4301581.
43. ^ Zhao YB, Zhang Y, Zhang QC, Li HJ, Cui YQ, Xu Z, Jin L, Zhou H, Zhu H (2015). "Ancient DNA reveals that the genetic structure of the northern Han Chinese was shaped prior to 3,000 years ago". PLOS ONE. 10 (5): e0125676. Bibcode:2015PLoSO..1025676Z. doi:10.1371/journal.pone.0125676. PMC 4418768. PMID 25938511.
44. ^ Yao YG, Kong QP, Bandelt HJ, Kivisild T, Zhang YP (March 2002). "Phylogeographic differentiation of mitochondrial DNA in Han Chinese". American Journal of Human Genetics. 70 (3): 635–51. doi:10.1086/338999. PMC 384943. PMID 11836649.
45. ^ Kivisild T, Tolk HV, Parik J, Wang Y, Papiha SS, Bandelt HJ, Villems R (October 2002). "The emerging limbs and twigs of the East Asian mtDNA tree". Molecular Biology and Evolution. 19 (10): 1737–51. doi:10.1093/oxfordjournals.molbev.a003996. PMID 12270900.
46. ^ Yao YG, Kong QP, Man XY, Bandelt HJ, Zhang YP (February 2003). "Reconstructing the evolutionary history of China: a caveat about inferences drawn from ancient DNA". Molecular Biology and Evolution. 20 (2): 214–9. doi:10.1093/molbev/msg026. PMID 12598688.
47. ^ Kong QP, Sun C, Wang HW, Zhao M, Wang WZ, Zhong L, Hao XD, Pan H, Wang SY, Cheng YT, Zhu CL, Wu SF, Liu LN, Jin JQ, Yao YG, Zhang YP (January 2011). "Large-scale mtDNA screening reveals a surprising matrilineal complexity in east Asia and its implications to the peopling of the region". Molecular Biology and Evolution. 28 (1): 513–22. doi:10.1093/molbev/msq219. PMID 20713468.
48. ^ Zhang Chi; Hsiao-Chun Hung (Fall 2008). "The Neolithic of Southern China-Origin, Development, and Dispersal". Asian Perspectives. 47 (2): 299–329. doi:10.1353/asi.0.0004. hdl:10125/17291. S2CID 162258899.
49. ^ Shelach, Gideon (December 2000). "The Earliest Neolithic Cultures of Northeast China: Recent Discoveries and New Perspectives on the Beginning of Agriculture". Journal of World Prehistory. 14 (4): 363–413. doi:10.1023/A:1011124209079. S2CID 161599532.
50. ^ Zhang Chi; Hsiao-chun Hun (March 2010). "The emergence of agriculture in southern China". Antiquity. 84 (323): 11–25. doi:10.1017/S0003598X00099737. S2CID 87789369.
51. ^ Higham, C.F.W.; Xie Guangmao; Lin Qiang (June 2011). "The prehistory of a Friction Zone: first farmers and hunters-gatherers in Southeast Asia". Antiquity. 85 (328): 529–543. doi:10.1017/S0003598X00067922. S2CID 162768159.
52. ^ Aldenderfer, Mark; Zhang Yinong (March 2004). "The Prehistory of the Tibetan Plateau to the Seventh Century A.D.: Perspectives and Research from China and the West Since 1950". Journal of World Prehistory. 18 (1): 1–55. doi:10.1023/B:JOWO.0000038657.79035.9e. S2CID 154022638.
53. ^ Blench, Roger. 2009. If agriculture cannot be reconstructed for Proto-Sino-Tibetan, what are the consequences?. Paper presented at the 42nd International Conference on Sino-Tibetan Language and Linguistics (ICSTLL 42), Chiang Mai, November 2–4, 2009. (slides)
54. ^ Sagart, Laurent; Jacques, Guillaume; Lai, Yunfan; Ryder, Robin; Thouzeau, Valentin; Greenhill, Simon J.; List, Johann-Mattis (2019). "Dated language phylogenies shed light on the ancestry of Sino-Tibetan". Proceedings of the National Academy of Sciences of the United States of America. 116 (21): 10317–10322. Bibcode:2019PNAS..11610317S. doi:10.1073/pnas.1817972116. PMC 6534992. PMID 31061123.
55. ^ Black ML, Wise CA, Wang W, Bittles AH (June 2006). "Combining genetics and population history in the study of ethnic diversity in the People's Republic of China". Hum. Biol. 78 (3): 277–93. doi:10.1353/hub.2006.0041. PMID 17216801. S2CID 42002729.

* v
* t
* e

Human genetics

Sub-topics|

* Human genome
* Human Genome Project
* Evolutionary genetics
* Human-chimp MRCA
* Neanderthal genetics
* Neanderthal genome project
* Timeline
* Genetic variation
* Blood type distribution by country
* Genealogical DNA test
* Genetic genealogy
* Race and genetics
* Recent evolution
* Surname DNA project
* Genetic enhancement

Genetic history
by region|

* Africa
* North Africa
* West Africa‎‎
* Central Africa
* Eastern Africa‎‎
* Southern Africa
* African diaspora
* South Asia
* India
* Middle East
* Early Anatolian farmers
* Caucasus
* Caucasus hunter-gatherer
* Europe
* Early European Farmers
* Western hunter-gatherer
* British Isles
* Iberia
* Italy
* Eastern hunter-gatherer
* Central Asia
* Ancient North Eurasian
* East Asia
* Ancient Northeast Asian
* Ancient Paleo-Siberian
* China
* Southeast Asia
* Thailand
* America
* Ancient Beringian

Population genetics
by group|

* Europe
* Basques
* Bosniaks
* Bulgarians
* Croats
* Romanians
* Russians
* Sami
* Serbs
* Azerbaijanis
* Jews
* Turks
* MENA
* Arabs
* Egyptians
* Moroccans
* South Asia
* Gujaratis
* Sinhalese
* Tamils (Sri Lankan)
* East Asia
* Han Chinese
* Japanese
* Southeast Asia
* Filipinos
* Sub-Saharan Africa
* Hutu/Tutsi

* Category

*[v]: View this template
*[t]: Discuss this template
*[e]: Edit this template