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mtDNA · 母亲 lineage

A11A

mtDNA Haplogroup A11A

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

mtDNA 谱系分支 A11A 的历史背景

Origins and Evolution

mtDNA haplogroup A11A is a downstream branch of haplogroup A11, itself a member of the broader haplogroup A1 clade that diversified in northeastern/East Asia during the early Holocene. Based on its phylogenetic position under A11 and the geographic pattern of related lineages, A11A most likely arose in the coastal or near-coastal regions of the Russian Far East / northern Japan area approximately ~8 thousand years ago (kya). The lineage is characterized by a small number of defining mitochondrial control-region and coding-region mutations (reported in limited sequencing studies), and it appears to have remained at low frequency and geographically localized compared with more widespread East Asian mtDNA clades.

Genetic and population-genetic evidence suggests A11A persisted primarily among maritime hunter-gatherer groups and their descendants, with limited downstream diversification visible in modern sampling. The scarcity of A11A in large modern datasets implies either a historically small effective population size for carriers or loss/absorption into expanding neighboring populations over the Holocene.

Subclades (if applicable)

At present, A11A is recognized as a narrow subclade of A11 with few well-differentiated downstream branches reported in public databases. Coverage is limited: deep whole-mitogenome sequencing of additional individuals will be needed to resolve any internal substructure reliably. Because of the small sample size, many reported A11A assignments come from hypervariable-region (HVR) or partial-sequence matches; robust coding-region variation or complete-mitogenome phylogenies remain the best path to identify and validate subclades.

Geographical Distribution

A11A shows a geographically focused distribution centered on the Russian Far East and northern Japan, with occasional low-frequency occurrences across northeast Asia. Populations and regions with reported A11A (or closely related A11 lineages) include:

  • Indigenous Siberian groups of the Russian Far East (for example, Nivkh, Ulchi and related coastal groups).
  • Northern Japanese populations with elevated Jomon or Ainu-related ancestry (sporadic occurrences reflecting continuity or admixture with mainland groups).
  • Northeast Asian populations (very low frequency) including northern Han Chinese, Koreans and Mongolian groups in certain localities.
  • Extremely rare detections reported in some Central Asian or neighboring groups, typically at very low frequency and often attributable to recent gene flow or sampling noise.

Ancient DNA evidence for A11A is currently limited; at least one ancient individual with A11-class mtDNA has been reported in published aDNA datasets from coastal Northeast Asia, consistent with an origin and continuity in maritime hunter-gatherer populations.

Historical and Cultural Significance

Because A11A is concentrated in coastal and northern areas, it is particularly informative for reconstructing maternal ancestry among Jomon, Okhotsk, and other Holocene coastal hunter-gatherer cultures in the Russian Far East and northern Japan. Its presence in modern Ainu- and Jomon-admixed populations aligns with archaeological and genomic models in which localized maternal lineages persisted among island and coastal communities even as mainland populations shifted during the Neolithic and Bronze Age.

A11A's low frequency in broad sampling suggests it did not participate in large-scale expansions that spread other East Asian mtDNA lineages (for example, agricultural-associated expansions). Instead, A11A more likely reflects long-term regional continuity, population structure, and localized demographic histories (small effective sizes, founder effects, and genetic drift) in high-latitude coastal environments.

Conclusion

mtDNA haplogroup A11A is a rare, regionally concentrated maternal lineage derived from A11 that provides a focused window onto the maternal genetic landscape of Holocene coastal Northeast Asia. While current data are limited, A11A is best interpreted as part of the legacy of northern coastal hunter-gatherer populations (including Jomon- and Okhotsk-affiliated groups) and merits further sampling and complete-mitogenome sequencing to clarify its substructure, age, and historical dynamics.

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 A11A。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 A11A 当前 ~8,000 years ago Neolithic 8,000 years 0 0 1
2 A11 ~12,000 years ago Neolithic 12,000 years 1 2 0
3 AA - - - 4 947 0
4 A ~30,000 years ago Paleolithic 30,000 years 4 997 192
5 N ~60,000 years ago Paleolithic 60,000 years 16 26,150 13
6 L3 ~70,000 years ago Paleolithic 70,000 years 7 30,162 6
7 L3'4 - - - 2 30,212 0
8 L3'4'6 - - - 2 30,216 0
9 L2'3'4'6 - - - 2 31,333 0
10 L2'3'4'5'6'7 - - - 2 31,349 0
11 L1'2'3'4'5'6'7 - - - 2 31,852 0
12 L ~160,000 years ago Paleolithic 160,000 years 2 32,236 5

Subclades (0)

终端分支 -没有记录的子密钥

参考简介

哪里是这个世界

地理分布和现代存在

记录来源

Northeast/East Asia (Russian Far East / northern Japan)

现代发行

The populations where mtDNA haplogroup A11A is found include:

  1. Indigenous Siberian and Russian Far East coastal groups (e.g., Nivkh, Ulchi, Itelmen)
  2. Northern Japanese populations with Jomon/Ainu ancestry
  3. Northeast Asian groups at low frequency (northern Han Chinese, Koreans, Mongolians)
  4. Selected Central Asian and neighboring East Asian groups at very low frequency
  5. Modern descendant communities in the Russian Far East and Hokkaido with elevated hunter-gatherer ancestry
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. ~8k 年前

    Haplogroup A11A

    此 mtDNA 分支的形成时间为推定值,日期和地点仅作参考。

    这个分支
  3. ~5k 年前

    青铜时代

    金属加工、书写和早期文明

  4. ~3k 年前

    铁器时代

    铁工具,扩大贸易网络

  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 mtDNA 分支 A11A 考古关联

有记录的协会

这些标签描述与 A11A 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。

Caishichang Culture China_Tibet_Qulongsazha_IA Kitoi Kuenga Culture Lokomotiv Culture Mongolian Ob River Culture Russia_AltaiKrai_N Russia_Novosibirsk_N-1 Umungobi Medieval
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 A11A 的直接携带者 1 名

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 mtDNA 匹配
AI生成的示例性肖像 Omnogovi Late Medieval individual, Umungobi. Ganzagad, Mongolia (1,000-1,500 CE)
Sample ID: GAN002
Mongolia Late Medieval Umungobi, Mongolia 1000-1500 CE Umungobi Medieval A11a Direct
MATERNAL 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 A11A 及其下游分支的携带者

直接承运人
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 2026-02-16
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。