跳转到主内容
mtDNA · 母亲 lineage

L2A1C3B1

mtDNA Haplogroup L2A1C3B1

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 L2A1C3B1 的历史背景

Origins and Evolution

mtDNA haplogroup L2A1C3B1 is a terminal/subterminal branch within the broader L2a clade, descending from L2A1C3B. Based on its phylogenetic position and the distribution of closely related lineages, it most likely arose in West/Central Africa during the Late Holocene (around 1.2 kya). As a relatively recent daughter clade of L2a lineages that diversified throughout the Holocene, L2A1C3B1 reflects local diversification within populations that were involved in Late Holocene demographic processes across West and Central Africa.

Mutational accumulation that defines L2A1C3B1 is consistent with a shallow time depth relative to deeper African mtDNA branches (such as early L1 or L2 splits). The limited number of downstream branches and its detection at low-to-moderate frequencies in multiple populations suggests a pattern of local expansion followed by dispersal through both prehistoric and historic population movements.

Subclades

At present L2A1C3B1 appears to be a relatively terminal subclade (few or no widely recognized downstream named branches). Because this is a deep nomenclature within a localized lineage, future sequencing surveys—especially full mitochondrial genomes from understudied West and Central African groups and from African-descended populations in the Americas and Atlantic islands—may reveal additional substructure or newly named downstream clades.

Geographical Distribution

Primary distribution: West and Central Africa, where it is most frequently observed among coastal West African groups (e.g., Yoruba, Akan) and among various Bantu-speaking populations in Central Africa.

Secondary distribution: Lower-frequency occurrences extend to Eastern and Southern African Bantu-speaking communities through historical Bantu migrations and more recent gene flow. Historic movements, particularly the Atlantic slave trade, account for the presence of L2A1C3B1 in African-descended populations of the Americas and Caribbean, and in Atlantic-island populations such as Cape Verde.

Archaeogenetic evidence: L2A1C3B1 has limited representation in ancient DNA datasets (recorded in a small number of archaeological samples in curated databases), reflecting both its relatively recent origin and the current geographic and taphonomic biases in African ancient DNA research.

Historical and Cultural Significance

L2A1C3B1's primacy among Bantu-speaking and coastal West African groups ties it to the demographic history of the last two to three millennia in sub-Saharan Africa. While the broader Bantu expansion (beginning several thousand years ago) dispersed many maternal lineages across much of sub-Saharan Africa, L2A1C3B1 likely represents a later, regionally concentrated diversification that was carried during subsequent local expansions and the complex web of migrations and trade networks along the West African littoral.

The trans-Atlantic slave trade (ca. 0.4–0.5 kya) is the primary historical mechanism explaining the appearance of L2A1C3B1 in the Americas, Caribbean, and Atlantic islands. Founder effects and genetic drift in island and diaspora populations (for example Cape Verdean communities and Afro-Caribbean groups) can raise the relative frequency of this lineage locally, even if it remains uncommon at the continental scale outside Africa.

Conclusion

L2A1C3B1 is a recent, regionally focused maternal lineage rooted in West/Central Africa that illustrates how Late Holocene demographic processes and historic events shaped maternal genetic diversity. Continued sampling—particularly full mitogenomes from under-sampled African populations and from historical-era remains—will refine the internal structure and precise dispersal history of this haplogroup.

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 L2A1C3B1。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 L2A1C3B1 当前 ~1,000 years ago Medieval 1,200 years 0 0 0
2 L2A1C3B ~1,000 years ago Medieval 1,200 years 1 0 1
3 L2A1C3 ~3,000 years ago Iron Age 3,000 years 2 3 0
4 L2A1C ~6,000 years ago Chalcolithic 6,000 years 1 134 0
5 L2A1A ~8,000 years ago Neolithic 8,000 years 4 341 4
6 L2A1 ~18,000 years ago Mesolithic 18,000 years 2 606 0
7 L2A1'2'3'4 - - - 2 616 0
8 L2A ~50,000 years ago Paleolithic 50,000 years 2 642 12
9 L2A'B'C'D - - - 2 989 0
10 L2 ~70,000 years ago Paleolithic 70,000 years 4 1,045 7
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

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

West/Central Africa

现代发行

The populations where mtDNA haplogroup L2A1C3B is found include:

  1. Yoruba and other coastal West African groups (e.g., Akan)
  2. Various Bantu-speaking populations across Central Africa (e.g., Kongo-related groups)
  3. Central African rainforest populations (including some Pygmy-associated groups)
  4. Eastern and Southern African Bantu-speaking communities at lower frequencies
  5. African-descended populations in the Americas and the Caribbean (African American, Afro-Caribbean)
  6. Cape Verdean and other Atlantic-island populations with West African ancestry
  7. North African and some Middle Eastern groups at very low frequencies due to historical admixture
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. ~2.5k 年前

    古典时代

    希腊和罗马文明蓬勃发展

  5. ~1.2k 年前

    Haplogroup L2A1C3B1

    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
  6. 现

    现日

    现代时代

参考简介

考古学背景

已记录的 mtDNA 分支 L2A1C3B1 考古关联

有记录的协会

这些标签描述与 L2A1C3B1 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 Punic Sardinian El Argar Luxmanda Culture Makwasinyi Modern Period Mtwapa Nubian Christian Viterbo 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 L2A1C3B1 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 Sardinia IA a IA b Nuragic-1 individual, Sardinia. Villamar. VS. Villamar, Italy (788-551 BCE)
Sample ID: VIL006
Italy Iron Age Punic 1 Sardinia, Italy 788-551 calBCE (2530±20 BP) Early Punic Sardinian L2a1c3b1 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 L2A1C3B1 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。