AU77328
古人
hg38 / GRCh38
E11 欧洲 European: 54.83% 印度 India: 18.06% 鄂伦春 North Chinese Oroqen: 9.50% 雅库特 Yakut: 6.16% 美洲 American: 4.14% 日本 Japanese: 2.98% 非洲 African: 1.58% 马来 Malay: 1.07% 彝族 Southwest Chinese Yi: 1.06% 华东 East Chinese: 0.61% K47 东地中海 East-Med: 15.94% 东欧 East-Euro: 7.12% 北高加索 North-Caucasian: 6.87% 中地中海 Central-Med: 6.72% 古巴尔干 Paleo-Balkan: 6.58% 突厥－阿尔泰 Turkic-Altai: 6.55% 阿穆尔－满洲 Amuro-Manchurian: 5.22% 西地中海 West-Med: 4.98% 北伊比利亚 North-Iberian: 4.73% 伊朗 Iranian: 4.65% 南高加索 South-Caucasian: 4.16% 藏缅 Tibeto-Burman: 3.80% 蒙古 Mongolian: 3.68% 东伊比利亚 East-Iberian: 3.18% 北海日耳曼 North-Sea-Germanic: 3.13% 西伯利亚 Siberian: 2.73% 帕米尔 Pamirian: 2.55% 阿拉伯 Arabic: 2.33% 西北印度 NW-Indian: 1.86% 西芬兰 West-Finnic: 1.66% 凯尔特人 Celtic: 1.28% 安第斯 Andean: 0.24% 南非 South-African: 0.03% MichalK25 地中海 Mediterranean: 19.39% 高加索 Caucasian: 18.81% 德鲁兹人 Druzian: 12.56% 东北欧 Northeast European: 11.47% 东北亚 Northeast Asian: 9.64% 东亚 East Asian: 5.21% 阿拉伯 Arabic: 4.75% 柏柏尔人 Berberic: 2.85% 北印度 North Indian: 2.67% 阿尔泰 Altaic: 2.54% 乌拉尔 Uralic: 2.48% 爱斯基摩人 Eskimoic: 2.19% 西伯利亚 Siberian: 1.56% 卡拉什人 Kalash: 1.24% 堪察加 Kamchatkan: 0.73% 北美印第安人 North Amerindian: 0.62% 纳索伊人 Nasoic: 0.60% 台湾原住民 Taiwanese Aboriginal: 0.46% 蔻玛尼萨恩人 Khomani San: 0.22% K12b 高加索 Caucasus: 28.06% 大西洋地中海 Atlantic Med: 18.22% 北欧 North European: 14.34% 西伯利亚 Siberian: 11.46% 东亚 East Asian: 9.93% 西南亚 Southwest Asian: 8.43% 格德罗西亚 Gedrosia: 7.61% 南亚 South Asian: 1.34% 撒哈拉以南非洲 Sub Saharan: 0.59% 西北非 Northwest African: 0.02% puntDNAL 新石器时代安纳托利亚 Anatolian Neolithic: 31.70% 欧洲狩猎采集者－大草原 EHG-Steppe: 15.92% 新石器时代伊朗 Iran Neolithic: 13.29% 西伯利亚 Siberian: 12.98% 西方狩猎采集者 Western HG: 9.47% 东欧亚 East Eurasian: 7.87% 纳吐夫狩猎采集者 Natufian HG: 5.73% 南欧亚 South Eurasian: 2.47% 撒哈拉以南非洲 Sub-Saharan: 0.57% AncientNearEast13 高加索狩猎采集者－早期欧洲农人 CHG-EEF: 22.41% 新石器时代安纳托利亚 Anatolia Neolithic: 20.36% 西伯利亚 Siberian: 12.40% 新石器时代伊朗 Iran-Neolithic: 11.43% 欧洲狩猎采集者 EHG: 11.15% 纳吐夫 Natufian: 9.23% 东南亚 Southeast Asian: 8.78% 斯堪的纳维亚－西欧狩猎采集者 SHG-WHG: 3.06% 原始印度人 Ancestral-Indian: 1.02% 极地 Polar: 0.16% EastSeaK12 欧洲 European: 56.87% 印度 Indian: 16.47% 雅库特 Yakuts: 9.62% 日本 Japanese: 5.29% 蒙古·通古斯 Mongolian-Tungusic: 4.99% 藏族 Tibetan: 4.20% 非洲 African: 1.91% 柬埔寨 Cambodian: 0.65% ProjectLiK11 西欧亚古波斯 West Eurasian / Ancient Persia: 53.94% 古代蒙古 Ancient Mongolia: 14.80% 美洲 American: 11.94% 东亚古黄河 East Asian / Ancient Yellow River: 7.82% 南印度伊鲁拉 South India / Irula: 3.00% 东亚古台湾(汉本) Ancient Taiwan / Hanben: 2.70% 非洲约鲁巴 African / Yoruba: 1.97% 尼泊尔古藏缅 Ancient Nepal: 1.59% 绳文 Jomon: 1.17% 古南岛瓦努阿图 Ancient Vanuatu: 0.79% 安达曼 Andaman: 0.30% ProLi14 古安纳托利亚农民 Ancient Anatolia Farmer: 30.24% 古东欧(卡累利亚共和国) Old East Euro(Karelia): 19.71% 古伊朗(扎格罗斯山脉) Old Iran(GanjDareh): 19.38% 古东北(黑龙江流域) Ancient NE Chinese(Devil's Gate): 8.66% 古蒙古北部 Old Mongolia North: 4.92% 南印度(伊鲁拉) South India(Irula): 4.41% 古华中(平粮台遗址) Old Central Chinese(Ping Liang Tai): 4.16% 古高原(尼泊尔) Old Nepal(Samdzong): 1.95% 古西欧猎人 Ancient Euro Hunter: 1.95% 古中亚(切尔木切克人) Chemurchek: 1.19% 非洲 African: 1.09% 绳文 Jomon: 0.82% 安达曼 Onge: 0.80% 古东南(汉本遗址) Old SE Chinese(Hanben): 0.73%
男
覆盖度38.09％ 平均深度5
科研机构
Austria
Vienna
Avar
After a long-distance migration from the East, Avar people of Eastern Asian ancestry arrived in Eastern Central Europe in 567/568 CE and encountered groups with very different, European ancestry1,2. We used ancient genome-wide data of 722 individuals and fine-grained interdisciplinary analysis of large 7th-8th c. CE neighboring cemeteries south of Vienna (Austria) to address the centuries-long impact of this encounter1,2. We found that the ancestry at one site (Leobersdorf) was and remained dominantly East-Asian-like, even 200 years after the Avar immigration, while the other site (Mödling) displays local, European-like ancestry. These two nearby sites exhibit very few links of direct biological relatedness, despite sharing a distinctive late-Avar culture3,4. We reconstructed 6-generation pedigrees at both sites linking together up to 450 closely-related individuals, allowing per-generation demographic profiling of the communities. Despite different ancestry, these pedigrees together with large networks of distant relatedness display an absence of consanguinity, a strong patrilineal pattern with female exogamy, multiple reproductive partnerships (e.g. levirate) and direct correlation of social status to biological connectivity through markers of high social status in the archaeological material. The generation-long genetic barrier was maintained by systematically choosing partners with similar ancestry from other sites in the Avar realm. Leobersdorf had more biological connections with the Avar heartlands than Mödling, which is instead linked to another site from the Vienna Basin with European-like ancestry. Mobility between sites was mostly due to female exogamy pointing to different marriage networks as the main driver of the maintenance of the genetic barrier. 经过从东方的长途迁徙，东亚血统的阿瓦尔人于公元 567/568 年抵达中欧东部，并遇到了具有截然不同的欧洲血统的群体 1,2。我们使用了 722 个个体的古代全基因组数据和对维也纳（奥地利）南部 7-8 世纪大型邻近墓地的细粒度跨学科分析，以解决这次遭遇的数百年影响 1,2。我们发现，即使在阿瓦尔人移民 200 年后，其中一个地点（Leobersdorf）的血统仍然以东亚血统为主，而另一个地点（Mödling）则显示出当地的欧洲血统。这两个邻近的地点尽管共享独特的晚期阿瓦尔文化，但几乎没有直接的生物学关联 3,4。我们在两个遗址重建了 6 代谱系，将多达 450 名密切相关的个体联系在一起，从而可以对社区进行每代人口统计分析。尽管祖先不同，但这些谱系与大型远亲网络一起显示出没有血缘关系、强烈的父系模式和女性外婚、多重生殖伙伴关系（例如娶寡嫂制）以及社会地位与生物连通性的直接相关性，通过考古材料中的高社会地位标记。通过系统地从阿瓦尔王国的其他遗址中选择具有相似血统的伴侣，维持了长达一代的遗传屏障。莱奥伯斯多夫与阿瓦尔中心地带的生物联系比莫德林多，后者与维也纳盆地的另一个具有欧洲血统的遗址有关。遗址之间的流动主要是由于女性外婚，这表明不同的婚姻网络是维持遗传屏障的主要驱动力。
Ancient DNA reveals reproductive barrier despite shared Avar-period culture
© 2020-2023 TheYtree.com