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mtDNA · 母亲 lineage

R9C1B

mtDNA Haplogroup R9C1B

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 R9C1B 的历史背景

Origins and Evolution

R9C1B is a daughter clade of mtDNA haplogroup R9C1, itself nested within the broader R9/R haplogroup cluster that is characteristic of East and Southeast Asia. Based on its phylogenetic position beneath R9C1 (parent clade estimated ~14 kya) and the geographic concentration of modern carriers, R9C1B most likely arose in southern China or adjacent Mainland Southeast Asia during the early Holocene (roughly ~9 kya in our estimate). This timing places its origin after the Last Glacial Maximum and concurrent with regional population expansions linked to improved Holocene climates and the beginnings of local plant cultivation.

Mutation patterns that define R9C1B are consistent with a localized branching event from R9C1; the clade shows limited deep diversification compared with older regional lineages, suggesting a relatively recent origin and expansion restricted to southern China and Mainland Southeast Asia.

Subclades

As a subclade of R9C1, R9C1B may itself contain smaller internal branches observed at low frequency in modern and ancient sampling. Published datasets and targeted sequencing of Southeast Asian mtDNA indicate R9C1 has multiple sublineages (e.g., R9C1A, R9C1B), with R9C1B representing one such geographically restricted branch. Because sampling in many parts of Mainland Southeast Asia and Island Southeast Asia remains incomplete, additional minor subclades of R9C1B may be discovered with deeper mitogenome sequencing of under-sampled groups.

Geographical Distribution

Contemporary population genetic surveys place R9C1B predominantly in:

  • Southern China (including border provinces and minority groups), where R9C1 overall shows its highest densities.
  • Mainland Southeast Asian populations — notably Tai‑Kadai speaking groups (Dai, Zhuang), Austroasiatic speakers (Vietnamese, Khmer), and Thai/Lao populations — at moderate frequency.
  • Island Southeast Asia and some Austronesian-speaking groups (Taiwan indigenous groups, Philippines, parts of Indonesia) only at low to sporadic frequencies, consistent with limited transfer during Austronesian dispersals.
  • Very low, intermittent occurrences in Near Oceania, recorded in a small number of modern or ancient samples.

One ancient DNA sample in available databases has been assigned to an R9C1 lineage, supporting Holocene antiquity of this regional maternal clade.

Historical and Cultural Significance

The geographic and temporal pattern of R9C1B is consistent with post‑LGM regional continuity in southern China and Mainland Southeast Asia and later demographic processes:

  • Neolithic associations: The early Holocene origin overlaps with the beginnings and spread of rice cultivation in the Yangtze and adjacent regions; R9C1B may reflect maternal lineages involved in local Neolithic transitions and demographic growth.
  • Mainland Southeast Asian peopling: Moderate frequencies among Tai‑Kadai and Austroasiatic groups suggest a role in population structure shaped by language spread, local admixture, and cultural transmission across the mainland.
  • Austronesian contact: Low levels of R9C1B in some Austronesian groups and ISEA populations are consistent with limited maternal gene flow from Mainland Southeast Asia into expanding Austronesian communities rather than representing a primary Austronesian lineage.

These associations make R9C1B useful for reconstructing maternal ancestry in southern China and Mainland Southeast Asia and for identifying signals of Neolithic and later interactions between mainland and island populations.

Conclusion

R9C1B is a regional, Holocene‑age maternal lineage that encapsulates aspects of post‑LGM persistence and Neolithic demographic change in southern China and Mainland Southeast Asia. Its distribution—concentrated on the mainland with sporadic island occurrences—reflects both continuity and limited dispersal events (including admixture during Austronesian expansions). Continued mitogenome sequencing of under-sampled Southeast Asian groups and ancient remains will refine the substructure and timing of R9C1B's diversification and help place it in finer archaeological and historical context.

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 R9C1B。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 R9C1B 当前 ~9,000 years ago Neolithic 9,000 years 1 6 2
2 R9C1 ~14,000 years ago Mesolithic 14,000 years 1 6 0
3 R9C ~22,000 years ago Mesolithic 22,000 years 1 6 0
4 R9 ~40,000 years ago Paleolithic 40,000 years 3 281 0
5 R ~55,000 years ago Paleolithic 55,000 years 17 22,830 57
6 NA - - - 1 22,830 0
7 N ~60,000 years ago Paleolithic 60,000 years 16 26,150 13
8 L3 ~70,000 years ago Paleolithic 70,000 years 7 30,162 6
9 L3'4 - - - 2 30,212 0
10 L3'4'6 - - - 2 30,216 0
11 L2'3'4'6 - - - 2 31,333 0
12 L2'3'4'5'6'7 - - - 2 31,349 0
13 L1'2'3'4'5'6'7 - - - 2 31,852 0
14 L ~160,000 years ago Paleolithic 160,000 years 2 32,236 5
参考简介

哪里是这个世界

地理分布和现代存在

记录来源

Southeast Asia / Southern China

现代发行

The populations where MTDNA haplogroup R9C1B is found include:

  1. Han Chinese (southern China, particularly border provinces and some minority groups)
  2. Dai and Zhuang (Tai‑Kadai speaking groups)
  3. Thai and Lao populations
  4. Vietnamese and Khmer (Austroasiatic / Mon‑Khmer groups)
  5. Austronesian-speaking groups (some Taiwanese indigenous peoples, Filipinos, Indonesians) at low to moderate frequency
  6. Malay populations and Sea Nomad communities (sporadic occurrences)
  7. Tibeto‑Burman southwestern groups (low frequency)
  8. Ethnic minorities in southern China and northern Mainland Southeast Asia
  9. Indigenous populations of Near Oceania (very low, intermittent occurrences)
  10. Sparse occurrences among broader East Asian populations
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. ~9k 年前

    Haplogroup R9C1B

    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 R9C1B 考古关联

有记录的协会

这些标签描述与 R9C1B 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。

Afanasievo Culture Boisman Chinese Epipaleolithic Ganj Dareh Culture Island Southeast Asian Culture Linear Pottery Culture Russia_Omsk_Eneolithic_Chernoozersky Santa Rosa Island Culture Sardinian Neolithic Taiwanese Iron Ust-Ishim Culture
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 R9C1B 的直接携带者 1 名,子分支携带者 1 名

2 显示 ^ 2 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 Fujian Qihe Cave Epipaleolithic individual, Fujian. Zhangping. Qihe Cave, China (9,798-9,407 BCE)
Sample ID: Qihe3
China Epipaleolithic China 9798-9407 calBCE (10050±30 BP) Chinese Epipaleolithic R9c1b Direct
AI生成的示例性肖像 Austronesian individual, Hanben. Blihun site, Taiwan (258-413 CE)
Sample ID: I3621
Taiwan Iron Age Taiwan 258 CE - 413 CE Taiwanese Iron R9c1b2 下游分支
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

2 个古代 DNA 样本的地理分布,涵盖 R9C1B 及其下游分支的携带者

直接承运人 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 2026-02-16
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。