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mtDNA · 母亲 lineage

Y1A1

mtDNA Haplogroup Y1A1

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 Y1A1 的历史背景

Origins and Evolution

mtDNA haplogroup Y1A1 is a downstream branch of Y1A, itself a rare lineage within macro-haplogroup Y that is concentrated in the northwestern Pacific Rim. Based on its phylogenetic position and the estimated time depth of its parent clade, Y1A1 most likely arose in Northeast Asia during the mid-Holocene (several thousand years after the Last Glacial Maximum). Its internal diversity is low, consistent with a relatively recent local diversification from Y1A and/or a population history marked by founder effects and restricted maternal population sizes in coastal and riverine groups.

Because Y1A and its subclades are uncommon and geographically restricted, Y1A1 is particularly useful as a marker for tracking postglacial coastal dispersals, island/coastal hunter-gatherer continuity, and interactions between populations around the Sea of Okhotsk and northern Japan.

Subclades

Y1A1 is a terminal or near-terminal branch within the Y1A structure in currently published phylogenies. Where multiple internal branches exist they show low sequence diversity, reflecting either a recent branching event or undersampling of small source populations. Future dense mitogenome sampling in northeastern Eurasia (Hokkaido, Sakhalin, Kamchatka and the Amur region) could reveal additional substructure within Y1A1 and clarify relationships to nearby Y1A subclades.

Geographical Distribution

The modern distribution of Y1A1 is strongly concentrated in Northeast Asian coastal and riverine groups. Highest relative frequencies are reported in small, geographically concentrated populations (for example, some Ainu and indigenous groups of the Russian Far East), with low to sporadic occurrences in mainland Japan, Korea and scattered low-frequency reports farther afield (Southeast Asia and rare trans‑Beringian detections in the Americas). The pattern—localized peaks plus scattered low-frequency occurrences—matches expectations for a lineage that expanded within a restricted coastal/ecological niche and occasionally moved with small-scale migrations or long-distance contacts.

Ancient DNA evidence for Y1A-lineages (including lineages close to Y1A1) has been recovered from a small number of archaeological contexts in northern Japan and the Russian Far East, consistent with continuity or recurrent presence of this maternal lineage among Jomon, Okhotsk, and later coastal cultures.

Historical and Cultural Significance

Because of its concentration among populations traditionally associated with the northern Japanese and Okhotsk cultural spheres, Y1A1 contributes to genetic signals interpreted as Jomon-related and Okhotsk-related ancestry in modern groups such as the Ainu and certain indigenous Siberian peoples (Nivkh, Ulchi-area groups). Its rarity and locality make it valuable for distinguishing local continuity from later, broad-scale migrations (for example, differentiating coastal hunter-gatherer contributions from agricultural expansions across East Asia).

Y1A1 is not a marker of large continent-spanning demographic events; instead it documents regional maternal continuity, founder effects, and coastal mobility in the northwestern Pacific during the Holocene.

Conclusion

Y1A1 is a geographically informative, low-frequency maternal lineage that likely arose in Northeast Asia in the mid-Holocene and is concentrated among coastal/riparian populations of Hokkaido, Sakhalin and the Russian Far East. Its limited diversity and patchy modern distribution reflect both recent origin and demographic processes (founder effects, small effective population sizes, and localized continuity). Continued mitogenome sequencing in northeastern Eurasia and expanded ancient DNA sampling will refine its internal topology and clarify its role in late Holocene population history of the northwestern Pacific.

关键点

  • Origins and Evolution
  • Subclades
  • 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 Y1A1。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 Y1A1 当前 ~4,000 years ago Bronze Age 4,000 years 0 0 0
2 Y1A ~6,000 years ago Chalcolithic 6,000 years 1 3 6
3 Y1 ~8,000 years ago Neolithic 8,000 years 2 7 1
4 Y ~11,000 years ago Neolithic 11,000 years 2 26 0
5 N9 ~25,000 years ago Paleolithic 25,000 years 3 178 0
6 N ~60,000 years ago Paleolithic 60,000 years 16 26,150 13
7 L3 ~70,000 years ago Paleolithic 70,000 years 7 30,162 6
8 L3'4 - - - 2 30,212 0
9 L3'4'6 - - - 2 30,216 0
10 L2'3'4'6 - - - 2 31,333 0
11 L2'3'4'5'6'7 - - - 2 31,349 0
12 L1'2'3'4'5'6'7 - - - 2 31,852 0
13 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 Asia / Far East Siberia

现代发行

The populations where mtDNA haplogroup Y1A1 is found include:

  1. Ainu and some northern Japanese populations (Hokkaido)
  2. Indigenous groups of the Russian Far East and Sakhalin (e.g., Nivkh, Ulchi-area groups)
  3. Siberian populations along the Amur, Kamchatka and adjacent regions (occasional reports among Even, Evenk and related groups)
  4. Mainland Japanese and Korean samples at low frequencies
  5. Scattered low-frequency occurrences in some Southeast Asian populations
  6. Very rare occurrences in North American samples consistent with trans‑Beringian connections
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. ~4k 年前

    Haplogroup Y1A1

    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
  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 Y1A1 考古关联

有记录的协会

这些标签描述与 Y1A1 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。

Early Avar Gongguan Late Medieval Mongolian Mongol Tasmola
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 Y1A1 的直接携带者 6 名

6 显示 ^ 6 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 Early Avar-o High East Asia individual, Csongrád-Csanád County. Apátfalva-Nagyútdűlő, Hungary (630-660 CE)
Sample ID: AN-376
Hungary Hungary EarlyAvar 600-700 CE Early Avar Y1a1 Direct
AI生成的示例性肖像 Early Avar-o High East Asia individual, Danube-Tisza Interfluve. Kecskemét-Sallai út, Hungary (630-670 CE)
Sample ID: A1823
Hungary Early Avar Period Danube-Tisza, Hungary 600-700 CE Early Avar Y1a1 Direct
AI生成的示例性肖像 Early Avar individual, Csongrád-Csanád County. Szeged-FehértóA, Hungary (650-675 CE)
Sample ID: SZF-371
Hungary Hungary EarlyAvar 650-700 CE Early Avar Y1a1 Direct
AI生成的示例性肖像 EIA Tasmola individual, Birlik (Almaty) (Almaty Region, Talgar District), Kazakhstan (776-481 BCE)
Sample ID: BIR013
Kazakhstan Tasmola Culture 800-450 BCE Tasmola Y1a1 Direct
AI生成的示例性肖像 Khentii Late Medieval individual, Tavan Khailaast, Mongolia (1,299-1,409 CE)
Sample ID: TK5-8
Mongolia Mongol Empire 1299-1409 calCE (IAAA-130276) Mongol Y1a1 Direct
AI生成的示例性肖像 Khentii Late Medieval individual, Tavan Khailaast, Mongolia (1,330-1,442 CE)
Sample ID: TK5-2
Mongolia Mongol Empire 1330-1442 calCE (IAAA-150902) Mongol Y1a1 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

6 个古代 DNA 样本的地理分布,涵盖 Y1A1 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。