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Y-DNA · Paterno linaje

O1B1A1B

Y-DNA Haplogroup O1B1A1B

Um perfil de referência de um ramo de linhagem. Compartilhar haplogrupos não demonstra uma relação familiar ou uma identidade cultural.

Perfil de Referência

Contexto do ramo

Contexto histórico de la rama de linaje Y-DNA O1B1A1B

Origins and Evolution

Y-DNA haplogroup O1B1A1B is a subclade of O1B1A1, which itself belongs to the broader haplogroup O-M268 branch within the East Asian paternal tree. Based on the phylogenetic position of its parent lineage and the regional pattern of related clades, O1B1A1B likely formed in mainland East or Southeast Asia during the early Holocene, roughly around 15 thousand years ago.

This lineage is part of the major paternal diversification that occurred after the Last Glacial Maximum, when populations in southern East Asia expanded and differentiated. Like many branches of haplogroup O, its history is closely tied to population growth in southern China and adjacent regions, followed by later dispersals associated with farming communities, maritime movement, and language family expansions.

Subclades

As an intermediate clade, O1B1A1B serves as a connector between the broader parent lineage and any more derived downstream branches. Detailed phylogenetic resolution for this level may vary as new sequencing studies refine the tree, but in general it represents one of the regional offshoots within the O1B1A1 cluster rather than a deep basal lineage on its own.

Geographical Distribution

O1B1A1B is found primarily in East and Southeast Asia, with its highest relevance in populations historically connected to the southern East Asian genetic landscape. Its distribution is shaped by both ancient local diversification and later demographic expansions.

It is most commonly observed in:

  • Southern Han Chinese and related populations
  • Vietnamese and other mainland Southeast Asian populations
  • Tai-Kadai-speaking populations
  • Austroasiatic-speaking populations
  • Austronesian-speaking populations in Taiwan and Island Southeast Asia
  • Some Korean populations
  • Some Japanese populations
  • Selected Tibeto-Burman-speaking populations

The lineage is not typically considered a high-frequency marker across all of East Asia, but rather a regionally meaningful subclade that reflects the complex demographic history of southern China and its neighboring areas.

Historical and Cultural Significance

The broader O-M268 and O1 lineages are often associated with the spread of agricultural populations in East and Southeast Asia, especially communities linked to the growth of early rice farming and later regional expansions. While a specific direct archaeological attribution for O1B1A1B is not usually possible, its presence is consistent with the genetic landscape of populations involved in the formation and movement of southern Chinese, mainland Southeast Asian, and Austronesian-related groups.

This lineage may have participated indirectly in the demographic processes behind the spread of Tai-Kadai, Austroasiatic, and Austronesian populations, as well as later movements into neighboring regions such as the Korean Peninsula and Japan. As with many Y-DNA subclades in East Asia, its cultural relevance lies less in a single archaeological culture and more in the long-term interaction between population expansion, language dispersal, and regional admixture.

Relationship to Other Haplogroups

Within the East Asian paternal phylogeny, O1B1A1B is genealogically related to other subclades of haplogroup O, especially branches within O1B and neighboring O lineages that are frequent in East and Southeast Asia. These related clades often show geographic overlap rather than strict one-to-one cultural correspondence.

Conclusion

Y-DNA haplogroup O1B1A1B is a relatively specific East Asian paternal subclade that likely emerged in the early Holocene in mainland East or Southeast Asia. Its modern distribution reflects deep regional ancestry linked to the expansion of southern East Asian populations, with broad connections to farming, language spread, and the peopling of mainland and island Southeast Asia.

Pontos- Chave

  • Origins and Evolution
  • Subclades
  • Geographical Distribution
  • Historical and Cultural Significance
  • Relationship to Other Haplogroups
Perfil de Referência

Árvore e relações

Contexto filogenético e subclasse

Trajectória evolutiva

Sigue las ramas superiores registradas hasta O1B1A1B. Las fechas son estimaciones y pueden cambiar al revisarse los datos de referencia.

Passos Haplogrupo Antiguidade estimada Época arqueológica Tempo decorrido Subclasses imediatas Portadores modernos analisados Referências antigas
1 O1B1A1B Actual ~15,000 years ago Mesolithic 15,000 years 1 4 0
2 O1B1A1 ~15,000 years ago Mesolithic 15,000 years 2 55 0
3 O1B1A ~20,000 years ago Mesolithic 20,000 years 2 59 1
4 O1B1 ~25,000 years ago Paleolithic 25,000 years 1 59 0
5 O1B ~35,000 years ago Paleolithic 35,000 years 2 75 0
6 O1 ~45,000 years ago Paleolithic 45,000 years 2 132 8
7 O ~45,000 years ago Paleolithic 45,000 years 2 553 6
8 NO ~45,000 years ago Paleolithic 45,000 years 4 801 12

Ramas hermanas (1)

Outros ramos do mesmo haplogrupo superior

Perfil de Referência

No mundo

Distribuição geográfica e presença moderna

Origem registada

Mainland East or Southeast Asia

Distribuição moderna

The populations where Y-DNA haplogroup O1B1A1B is found include:

  1. Southern Han Chinese and related populations
  2. Vietnamese and other mainland Southeast Asian populations
  3. Tai-Kadai-speaking populations
  4. Austroasiatic-speaking populations
  5. Austronesian-speaking populations in Taiwan and Island Southeast Asia
  6. Some Korean populations
  7. Some Japanese populations
  8. Selected Tibeto-Burman-speaking populations

Presença regional

East Asia (southern China, Taiwan, Japan) Moderate
Southeast Asia (Maritime & Mainland) Moderate
Near Oceania / Island Melanesia Low
South Asia (coastal, occasional) Low
Central Asia (sporadic) Low
Eastern Asia High
Southeast Asia High
Northeast Asia Low
Island East Asia Moderate
Contexto Histórico

Uma ramificação através do tempo

Formação estimada em uma cronologia histórica ampla. Os marcadores temporais contribuem contexto e não implicam relação com culturas concretas.

  1. ~20k años de antigüedad

    Último máximo glacial

    Máxima extensão da última glaciação e isolamento de populações

  2. ~15k años de antigüedad

    Haplogrupo O1B1A1B

    Formação estimada deste ramo Y-DNA; as datas e localizações são estimativas de referência.

    Este ramo
  3. ~10k años de antigüedad

    Revolução neolítica

    Início da agricultura e formação de comunidades sedentárias

  4. ~5k años de antigüedad

    Idade do Bronze

    Metalurgia, escrita e primeiras civilizações

  5. ~3k años de antigüedad

    Idade do Ferro

    Ferramentas de ferro e ampliação de redes comerciais

  6. ~2.5k años de antigüedad

    Antiguidades clássicas

    Desenvolvimento das civilizações grega e romana

  7. Actualidad

    Actualidad

    Idade moderna

Perfil de Referência

Contexto arqueológico

Asociaciones arqueológicas registradas para la rama Y-DNA O1B1A1B

Associações registradas

Esses rótulos descrevem os contextos arqueológicos registrados para as amostras de referência vinculadas a O1B1A1B. Uma associação não demonstra que todos os portadores pertenceram a uma cultura ou seguiram uma rota migratória específica.

Balong Culture Cambodian Iron Age China_EBA China_EIA China_IA_Hellenistic China_Shandong_Dinggong_LN Qinchang Culture Tang Culture Yellow River Culture
As atribuições culturais baseiam-se no contexto arqueológico das amostras de DNA antigo e podem representar associações regionais de períodos concretos.
PATERNAL LINHAGEM · DNA ANTIGO

Mapa de testes de linhagems antigos

Siga os clados superiores até este ramo e explora onde se encontraram portadores antigos.

A carregar as observações antigas...

Os marcadores são locais de achados arqueológicos. Uma linha de descontínua representa uma transição geográfica proposta e incerta entre ramos consecutivos, apoiada em várias observações fechadas; não é uma rota de viagem exata, um local de nascimento ou um teste de descendência direta. As amostras do clado parental podem pertencer a outros ramos descendentes. As datas das amostras são distintas das datas de formação dos haplogrupos são mantidas.

Dados

Dados e proveniência

Informações sobre fontes e qualidade dos dados

Última actualização 2026-06-17
Pontuação de confiança 50/100
Cobertura Low

Fonte de Dados

A classificação, as datas estimadas e o contexto geográfico refletem os dados de referência registrados e podem mudar ao revisar os testes. A cobertura de amostras é desigual; os locais registrados e as associações arqueológicas não estabelecem a origem pessoal nem a identidade cultural.