2009
DOI: 10.1002/ajpa.21155
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Genetic perspectives on forager‐farmer interaction in the Luangwa Valley of Zambia

Abstract: The transformation from a foraging way of life to a reliance on domesticated plants and animals often led to the expansion of agropastoralist populations at the expense of hunter-gatherers (HGs). In Africa, one of these expansions involved the Niger-Congo Bantu-speaking populations that started to spread southwards from Cameroon/Nigeria approximately 4,000 years ago, bringing agricultural technologies. Genetic studies have shown different degrees of gene flow (sometimes involving sex-biased migrations) between… Show more

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Cited by 30 publications
(10 citation statements)
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“…This filtering resulted in 13 populations overlapping between mtDNA and the NRY, and we refer to this dataset as the “AU‐NBZ dataset” (Supporting Information Table S2). The analysis of the intensity of the sex‐biased gene flow (ISBGF) included additional data from southern African populations for which both mtDNA and NRY haplogroup frequencies were previously published (Barbieri, Butthof, Bostoen, & Pakendorf, ; Coelho, Sequeira, Luiselli, Beleza, & Rocha, ; de Filippo, Heyn, Barham, Stoneking, & Pakendorf, ; Henn et al, ; Marks et al, ; Schlebusch et al, ), and we refer to this as the “SA dataset” (Supporting Information Table S3). The highly admixed Karretjie and Colesberg Coloured populations from South Africa were treated as Khoisan populations in this analysis as they are likely to be partly descended from Khoisan populations (see Schlebusch et al, ; Traill, ).…”
Section: Methodsmentioning
confidence: 99%
“…This filtering resulted in 13 populations overlapping between mtDNA and the NRY, and we refer to this dataset as the “AU‐NBZ dataset” (Supporting Information Table S2). The analysis of the intensity of the sex‐biased gene flow (ISBGF) included additional data from southern African populations for which both mtDNA and NRY haplogroup frequencies were previously published (Barbieri, Butthof, Bostoen, & Pakendorf, ; Coelho, Sequeira, Luiselli, Beleza, & Rocha, ; de Filippo, Heyn, Barham, Stoneking, & Pakendorf, ; Henn et al, ; Marks et al, ; Schlebusch et al, ), and we refer to this as the “SA dataset” (Supporting Information Table S3). The highly admixed Karretjie and Colesberg Coloured populations from South Africa were treated as Khoisan populations in this analysis as they are likely to be partly descended from Khoisan populations (see Schlebusch et al, ; Traill, ).…”
Section: Methodsmentioning
confidence: 99%
“…The level of admixture differs considerably among populations; in particular, substantial proportions of mtDNA haplogroups L0d and/or L0k are observed in the pastoralist Kuvale from southwestern Angola [21], in the Fwe of southwestern Zambia [20], and in the Zulu and Xhosa from South Africa [24]. In contrast, in populations from eastern Zambia, Zimbabwe, and Mozambique these characteristic autochthonous haplogroups are found at a frequency of at most 3% [19], [25], [26].…”
Section: Introductionmentioning
confidence: 99%
“…Within the past ∼4000 years, Bantu speakers from West Africa practicing agricultural subsistence migrated throughout subSaharan Africa and subsequently admixed with indigenous populations (Ehret 1998; Tishkoff et al 2009). This expansion greatly influenced genomewide patterns of genetic variation in modern African populations, an impact that can be observed readily in studies of mitochondrial loci (Soodyall et al 1996; Behar et al 2008; Quintana Murci et al 2008; Castri et al 2009), Ychromosome DNA (Poloni et al 1997; Hammer et al 2001), or both (Passarino et al 1998; Wood et al 2005; Tishkoff et al 2007, 2009; Pilkington et al 2008; Coelho et al 2009; de Filippo et al 2009). A classic example of positive natural selection in African populations involves a singlebase mutation upstream of FY , the gene encoding the Duffy blood group system.…”
mentioning
confidence: 99%