跳转到主内容
Y-DNA · 父权 lineage

E1B

Y-DNA Haplogroup E1B

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 E1B 的历史背景

Origins and Evolution

Y-DNA haplogroup E1B is a downstream node of the broader haplogroup E1 clade that expanded within Africa after the initial emergence of E1. Estimates for the origin of E1B place it in Northeast/East Africa during the Late Upper Paleolithic to early post-glacial interval (roughly ~30 kya, noting that published age estimates vary by method and marker sets). As a branching point it precedes the major, geographically differentiated subclades that dominate different parts of Africa and later influence surrounding regions.

Evolutionary studies and phylogenetic reconstructions indicate that E1B is ancestral to or closely related with the lineages that later diversified into both the widespread West/Central African lineages and the North African / Mediterranean–Near Eastern lineages. This topology explains why descendant lineages of this node are common across very different ecological and cultural zones.

Subclades

E1B is best understood as an intermediate branching point that gave rise to several major downstream clades (nomenclature varies between different build versions of the Y-tree). Important descendant groups commonly associated with this node include:

  • E-M2 (often listed historically as E1b1a / E-V38 branch) — dominant in West, Central and much of Southern Africa and strongly associated with the Bantu expansion.
  • E-M35 (often listed historically as E1b1b / E-M215 branch) — frequent in Northeast Africa, the Horn, North Africa, parts of the Near East and southern Europe, with many regional subclades (e.g., M78, M81, V13) that have their own demographic histories.

Because nomenclature has changed over time (different research groups use different labels and marker sets), it is important to consult the latest Y-chromosome phylogeny for exact subclade names and SNP definitions. In functional terms, E1B is a transitional node linking deep African diversity with lineages that later spread into adjacent regions.

Geographical Distribution

The descendant lineages that emerged from E1B have a broad distribution:

  • High frequencies across many sub-Saharan populations (via E-M2 and related branches), especially among West and Central African groups and in populations that expanded during the Bantu migrations.
  • High to moderate frequencies in the Horn and Northeast Africa, where several E-M35-derived subclades are common.
  • Significant presence in North Africa and the Sahel, including among Berber (Amazigh) groups where particular subclades (e.g., M81) are frequent.
  • Lower but detectable frequencies in the Near East and southern Europe, reflecting prehistoric connections (Neolithic movements, later Bronze Age and historic gene flow) and the long-term contact across the Mediterranean.
  • Present in the Americas and Caribbean largely due to the transatlantic slave trade, where descendant lineages from sub-Saharan Africa are frequent in African-descended populations.

Regional frequencies and the relative contribution of particular subclades vary considerably; some branches reflect recent demographic expansions (e.g., Bantu-related spreads), while others reflect older Holocene or Late Pleistocene dynamics and migrations.

Historical and Cultural Significance

  • Bantu expansion: Descendant lineages of E1B (notably E-M2 branches) are closely tied to the demographic processes of the Bantu expansion (starting roughly 3–4 kya), which spread agriculture and ironworking across much of sub-Saharan Africa and carried these paternal markers widely.

  • Afroasiatic and North African histories: E-M35-derived lineages (from the broader E1B-associated radiation) are associated with populations speaking Afroasiatic languages in the Horn and parts of North Africa, and with historically documented movements between North Africa, the Near East and southern Europe across the Holocene.

  • Saharan and Neolithic connections: Some subclades show signatures consistent with Saharan and Sahelian Neolithic population processes and later pastoralist dispersals that shaped regional paternal variation.

  • Historical gene flow and diasporas: Mediterranean and Near Eastern presence of certain subclades reflects millennia of contact (trade, migration, colonization), while the presence of sub-Saharan descendant lineages in the Americas reflects recent historical events (transatlantic slave trade).

Conclusion

E1B functions as an important intermediate branch within the E1 lineage that links deep East African paternal ancestry to a wide set of descendant lineages with major demographic impacts across Africa and into neighboring regions. Its descendant clades document key episodes in human prehistory and history — from Late Pleistocene and Holocene population structure in Africa to the spread of agriculture, pastoralism and later historic movements. Ongoing refinement of the Y-chromosome phylogeny and broader sampling across Africa continue to clarify the timing, branching order and regional dynamics of E1B and its descendant lineages.

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 E1B。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 E1B 当前 ~30,000 years ago Paleolithic 30,000 years 1 1,583 0
2 E1 ~50,000 years ago Paleolithic 50,000 years 2 1,667 2
3 E ~50,000 years ago Paleolithic 50,000 years 3 1,813 3

Siblings (1)

来自同一父分支的分支( oplogroup)

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 Africa

现代发行

The populations where Y-DNA haplogroup E1B is found include:

  1. Yoruba and other West African groups
  2. Bantu-speaking populations across Central, Eastern and Southern Africa
  3. Mande and West African coastal groups
  4. Ethiopian, Somali and Horn of Africa populations
  5. Berber (Amazigh) groups of North Africa
  6. Levantine and Near Eastern populations (at lower frequencies)
  7. Southern European groups in Mediterranean regions (e.g., Sicily, Iberia) at low–moderate frequencies
  8. African-descended populations in the Americas and Caribbean (via transatlantic slave trade)

区域存在

Eastern Africa High
Northern Africa High
Western Africa Moderate
Central Africa Low
Western Asia / Near East Moderate
Southern Europe Low
North America (diaspora) Low
Northeast Africa High
Southern Africa Moderate
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. ~30k 年前

    Haplogroup E1B

    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
  2. ~20k 年前

    上一个冰川最大值

    上一个冰河时代的高峰,人口隔离

  3. ~10k 年前

    新石器革命

    农业开始,定居社区形成

  4. ~5k 年前

    青铜时代

    金属加工、书写和早期文明

  5. ~3k 年前

    铁器时代

    铁工具,扩大贸易网络

  6. ~2.5k 年前

    古典时代

    希腊和罗马文明蓬勃发展

  7. 现

    现日

    现代时代

参考简介

考古学背景

已记录的 Y-DNA 分支 E1B 考古关联

有记录的协会

这些标签描述与 E1B 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。

Austria_Avar Moroccan Transitional Natufian PPNB Roman Provincial Saint Martin Spain_LatePunic-oAfrica
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 E1B 的子分支携带者 37 名(当前选定的参考样本中没有直接携带者)

10 显示 ^ 37 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 Pastoral N individual, Gishimangeda Cave, Tanzania (47-113 BCE)
Sample ID: I13977
Tanzania Prehistoric in Tanzania 47 calBCE - 113 calCE (2005±20 BP, PSUAMS-5652) Tanzanian Prehistoric E1b1b1b2b2 下游分支
AI生成的示例性肖像 LSA individual, Victoria Nyanza. Kisumu. Jawuoyo Rockshelter, Kenya (84-211 BCE)
Sample ID: I8808
Kenya Kenya LSA 119-216 calCE (1895±15 BP, PSUAMS-4783) LSA Kenya E1b1b1a1b2 下游分支
AI生成的示例性肖像 Pastoral N IA-o individual, Gishimangeda Cave, Tanzania (200-1 BCE)
Sample ID: I13762
Tanzania Prehistoric and Iron Age in Tanzania 163-59 calBCE (2140±15 BP, PSUAMS-5458) Tanzania Multi-Period E1b1b1b2b2a1 下游分支
AI生成的示例性肖像 Pastoral N individual, Nyandarua. Ol Kalou, Kenya (215-326 BCE)
Sample ID: I12384
Kenya Kenya PastoralN 229-358 calCE (1800±20 BP, PSUAMS-4940) Pastoral Neolithic E1b1b1b2b2a1 下游分支
AI生成的示例性肖像 Pastoral N individual, Gishimangeda Cave, Tanzania (245-368 CE)
Sample ID: I13972
Tanzania Prehistoric in Tanzania 245-368 calCE (1780±25 BP, PSUAMS-5651) Tanzanian Prehistoric E1b1b1b2b2 下游分支
AI生成的示例性肖像 Alt Inden Early Medieval-o Levant individual, North Rhine-Westphalia. Alt-Inden, Germany (400-800 CE)
Sample ID: IND009
Germany Saxon Early Medieval Alt Inden, Germany 400-800 CE Saxon Culture E1b1b1a1b1a 下游分支
AI生成的示例性肖像 Pastoral N individual, Molo Cave. GoJi3, Kenya (437-600 BCE)
Sample ID: MOL001
Kenya Molo Cave Pastoral Neolithic in Kenya 541-637 calCE (1532±21 BP, OxA-37360) Molo Cave Culture E1b1b1b2b 下游分支
AI生成的示例性肖像 Pastoral N individual, Hyrax Hill. GrJj25, Kenya (513-386 BCE)
Sample ID: HYR002
Kenya Hyrax Hill Pastoral Neolithic in Kenya 415-202 calBCE (2354±23 BP, OxA-37352) Hyrax Hill E1b1b1b2b 下游分支
AI生成的示例性肖像 Piedmont North Early Medieval Lombards-3 individual, Piedmont. Collegno, Italy (580-630 CE)
Sample ID: CL38
Italy Early Medieval Langobards, Northern Italy 550-650 CE Langobard E1b1b1a1b1a3 下游分支
AI生成的示例性肖像 Berber individual, Tenerife, Canary Islands (593-660 CE)
Sample ID: gun012
Canary Islands The Guanche People of the Canary Islands 593 CE - 660 CE Guanche E1b1b1b1a1 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

37 个古代 DNA 样本的地理分布,涵盖 E1B 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。