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Y-DNA · 父权 lineage

C2A1A1B

Y-DNA Haplogroup C2A1A1B

一个家族分支的参考简介 。 共享haplogroups 无法建立家庭关系或文化认同 。

参考简介

部门背景

Y-DNA 谱系分支 C2A1A1B 的历史背景

Origins and Evolution

Y-DNA haplogroup C2A1A1B is a downstream branch within the broader C2 (M217) phylogeny, itself characteristic of northern and eastern Eurasia. Based on its position beneath C2A1A1 and the known time depth of that parent clade, C2A1A1B most plausibly arose in Central–East Asia in the later Holocene (approximately ~3.0 kya inferred), during a period of increased mobility on the steppe and intensifying interactions among forest-steppe, steppe and northern Siberian groups. Its emergence likely post-dates the initial C2 expansions of the Bronze Age and corresponds with regional differentiation tied to Iron Age and historic nomadic movements.

Like many C2 subclades, C2A1A1B exhibits a pattern of regional substructure and occasional high-frequency clustering in particular paternal lineages or clans within Mongolic, Tungusic and some Turkic-speaking populations. This pattern is consistent with serial founder effects, social structuring (patrilineal clans), and expansions mediated by pastoralist mobility.

Subclades (if applicable)

C2A1A1B sits beneath C2A1A1 and is one branch among several downstream lineages. Where high-resolution SNP or next-generation sequencing data are available, researchers typically observe that C2 lineages break into multiple geographically structured subclades; C2A1A1B represents one such lineage that has further local diversification within northern Eurasia. In population studies, subclades of C2 often show clan-level concentration (single-lineage amplifications) rather than uniform distribution across all populations, so C2A1A1B may include multiple closely related downstream clusters in different geographic pockets.

Geographical Distribution

C2A1A1B is primarily observed in northern and northeastern Eurasia, with highest frequencies and confidence in Central–East Asian and Siberian populations. Modern occurrences are concentrated among: Mongolic-speaking populations (e.g., Mongols, Buryats), Tungusic groups (e.g., Evenks, Evens, Oroqen), Yakut (Sakha) and other North Siberian peoples, and in varying frequency among southern Siberian Turkic groups (e.g., Tuvans, some Altai and Kazakh clans). Low-frequency occurrences have been reported in neighboring East Asian populations (Korean, Japanese) and extremely rare or secondary occurrences may be present in some Indigenous North American groups reflecting ancient Beringian connections or later drift.

Genetic surveys and ancient DNA studies of steppe and forest-steppe populations indicate that C2-derived lineages were important components of the paternal landscape of Bronze–Iron Age northern Eurasia, and specific downstream branches like C2A1A1B tend to reflect later, geographically localized differentiation and historic era expansions.

Historical and Cultural Significance

The demographic behavior of C2A1A1B is consistent with the social and migratory patterns of steppe pastoralist and forest-steppe societies: clan-based amplifications, elite-driven expansions, and mobility across large distances. Historically, groups associated with Iron Age and historic nomadic polities in Central–East Asia (e.g., Xiongnu, Xianbei-related groups, and later Turkic and Mongolic confederations) generated conditions that could amplify particular paternal lineages. The medieval Mongol Empire and related movements are especially important for redistributing C2 lineages across Eurasia, and local founder effects after migrations — for example, the northward movement and settlement of Yakut (Sakha) peoples — can explain high frequencies in northern pockets.

However, it is important to emphasize that attributing a haplogroup directly to any single archaeological culture or polity requires careful ancient DNA evidence; modern-day distributions reflect cumulative processes including prehistoric expansions, historic migrations, drift, and social structure.

Conclusion

C2A1A1B is a geographically and historically informative subclade of C2A1A1 that illuminates patterns of paternal ancestry across the northern Eurasian steppe, forest-steppe and Siberia. It likely arose in Central–East Asia around the Iron Age and shows clustered distribution in Mongolic, Tungusic and northern Turkic-speaking groups, with lower-frequency spillover into neighboring East Asian and, rarely, North American populations. As sequencing of modern and ancient samples expands, the internal diversity and precise historical movements of C2A1A1B will become clearer, refining its role in the peopling and social history of northern Eurasia.

关键点

  • Origins and Evolution
  • Subclades (if applicable)
  • Geographical Distribution
  • Historical and Cultural Significance
  • Conclusion
参考简介

树形关系( N)

phylgenetic 上下文和子拼写

进化路径

沿已记录的上级分支追溯至 C2A1A1B。年代为估计值,可能随参考数据更新而调整。

步骤 单倍群 年龄估计 考古时代 时间流逝 直系后裔 被测试的现代后裔 古代连接
1 C2A1A1B 当前 ~3,000 years ago Iron Age 3,000 years 1 0 0
2 C2A1A1 ~4,000 years ago Bronze Age 4,500 years 1 0 0
3 C2A1A ~6,000 years ago Chalcolithic 6,000 years 4 3 0
4 C2A1 ~12,000 years ago Neolithic 12,000 years 1 3 0
5 C2A ~18,000 years ago Mesolithic 18,000 years 1 38 0
6 C2 ~40,000 years ago Paleolithic 40,000 years 2 99 24
7 C ~60,000 years ago Paleolithic 60,000 years 3 406 35
参考简介

哪里是这个世界

地理分布和现代存在

记录来源

Central–East Asia

现代发行

The populations where Y-DNA haplogroup Y-DNA haplogroup C2A1A1B is found include:

  1. Mongolic-speaking groups (e.g., Mongols, Buryats)
  2. Tungusic peoples of Siberia (e.g., Evenks, Evens, Oroqen)
  3. Yakut (Sakha) and other North Siberian populations
  4. Southern Siberian Turkic groups (e.g., Tuvans, some Altai/Kazakh clans)
  5. Selected Northeast Asian populations (low-frequency occurrences in Korean and Japanese lineages)
  6. Very rare or sporadic occurrences in some Indigenous North American groups (secondary/rare)

区域存在

Northern Asia / Siberia High
Northeast Asia (Mongolia, Northeast China) High
Central Asia Low
East Asia (northern China, Korea) Low
Northern Siberia Moderate
Eastern Asia Low
North America (Indigenous) Low
历史背景

分枝穿越时间

大致历史时间范围内的估计形成情况:周期标志提供了背景,并不意味着与特定文化的联系。

  1. ~10k 年前

    新石器革命

    农业开始,定居社区形成

  2. ~5k 年前

    青铜时代

    金属加工、书写和早期文明

  3. ~3k 年前

    铁器时代

    铁工具,扩大贸易网络

  4. ~3k 年前

    Haplogroup C2A1A1B

    此 Y-DNA 分支的形成时间为推定值,日期和地点仅作参考。

    这个分支
  5. ~2.5k 年前

    古典时代

    希腊和罗马文明蓬勃发展

  6. 现

    现日

    现代时代

参考简介

考古学背景

已记录的 Y-DNA 分支 C2A1A1B 考古关联

有记录的协会

这些标签描述与 C2A1A1B 相关的参考样本所处的考古背景。仅凭这种关联,无法判断所有携带者都属于某种文化或沿同一路线迁徙。

Altai-Sayan Lokomotiv Culture Mongolian Neolithic Northern Mongolian Culture Ob River Culture Russia_AltaiKrai_Eneolithic Russia_Sakha_Mesolithic
文化任务基于古代DNA样本的考古背景,可能代表特定时期的区域协会.
参考简介

样本目录

单倍群 C2A1A1B 的子分支携带者 1 名(当前选定的参考样本中没有直接携带者)

1 显示 ^ 1 匹配样本

Portraits是AI生成的插图,样本标签和加入ID识别参考记录.

纵向 样本 国家 大纪元 日期 文化 Y-DNA 匹配
AI生成的示例性肖像 Xiongnu Empire individual, Uvs aimag. Ulaangom sum. Chandman Uul. Ulaangom cemetery Grave #44, Mongolia (40 BCE-109 CE)
Sample ID: I6228
Mongolia Early Iron Age Xiongnu Culture 7, Mongolia 40 BCE - 109 CE Xiongnu Culture C2a1a1b1b-Y11605 下游分支
PATERNAL LINEAGE · ANCIENT DNA

古代世系证据地图

跟随母舰飞向这个分支 探索古代载体的发现地点

正在装入古老的观测...

标记是考古发现地点。一个破碎的连接器是连续分支之间一种不确定的、拟议中的地理过渡,辅以多个日期的观察;它不是一个准确的旅行路线、出生地或直接血统的证明。父系样本可能属于其他后代分支。在证据不足的地方,差距依然存在。样本日期与随机群形成日期不同。

参考简介

载体分布图

1 个古代 DNA 样本的地理分布,涵盖 C2A1A1B 及其下游分支的携带者

子舱载体
时间段过滤器
所有时间段
显示全部样本
参考简介

时间分布

载体在考古时期的分布

参考简介

地理分布

按有记录的抽样国家计算,反映的是现有的参考选择,而不是人口频率。

参考简介

国家 × 大纪元发行

比较各国和考古时期记录的样本数量。选择一个人口密集的细胞来检查样本。

数据

数据证明( P)

来源信息和数据质量

上次更新 2026-06-15
信心分数 50/100
覆盖范围 Low

数据来源

分类、估计日期和地理背景反映了所记录的参考数据,随着证据的修订而可能发生变化,样本覆盖范围不均匀;所记录的地点和考古协会没有确定个人出身或文化特征。