oditous
2010-02-28, 22:59
Australoid admixture can be anything ranging from negrito, veddoid, papuan, australian aboriginal. Basically anything predating mongoloid migrations into SE Asia
I'll post some studies. But i'm also curious to know what your intuitive guesses might be.
Balinese Y-chromosome perspective on the peopling of Indonesia: genetic contributions from pre-neolithic hunter-gatherers, Austronesian farmers, and Indian traders (2005)
The observed frequencies of K-M9*, K-M230, and M-P34 on Bali suggest that 2.2% of the pre-Neolithic gene pool survived the invasion of AustronesianY chromosomes. Interestingly, a similar extent of replacement is evident in Java(3.8%), and a slightly higher proportion of pre-Neolithic Y chromosomes is ob-served in Borneo (15.0%) (Kayser et al. 2003). A similar analysis of our sample of eastern Indonesians indicates major pre-Neolithic (78.2%) and minor Aus-tronesian (21.8%) components of their paternal gene pool
Philippine mitochondrial DNA diversity: a populated viaduct between Taiwan and Indonesia? (2009)
Relatively little is known about the genetic diversity of the Philippine population, and this is an important gap in our understanding of Southeast Asian and Oceanic prehistory. Here we describe mitochondrial DNA (mtDNA) variation in 423 Philippine samples and analyze them in the context of the genetic diversity of other Southeast Asian populations. The majority of Philippine mtDNA types are shared with Taiwanese aboriginal groups and belong to haplogroups of postglacial and pre-Neolithic origin that have previously been identified in East Asian and Island Southeast Asian populations. Analysis of hypervariable segment I sequence variation within individual mtDNA haplogroups indicates a general decrease in the diversity of the most frequent types (B4a1a, E1a1a, and M7c3c) from the Taiwanese aborigines to the Philippines and Sulawesi, although calculated standard error measures overlap for these populations. This finding, together with the geographical distribution of ancestral and derived haplotypes of the B4a1a subclade including the Polynesian Motif, is consistent with southward dispersal of these lineages "Out of Taiwan" via the Philippines to Near Oceania and Polynesia. In addition to the mtDNA components shared with Taiwanese aborigines, complete sequence analyses revealed a minority of lineages in the Philippines that share their origins--possibly dating back to the Paleolithic--with haplogroups from Indonesia and New Guinea. Other rare lineages in the Philippines have no closely related types yet identified elsewhere
Genetic admixture history of Eastern Indonesia as revealed by Y-chromosome and mitochondrial DNA analysis. (2009)
Eastern Indonesia possesses more linguistic diversity than any other region in Southeast Asia, with both Austronesian (AN) languages that are of East Asian origin, as well as non-Austronesian (NAN) languages of likely Melanesian origin. Here, we investigated the genetic history of human populations from seven eastern Indonesian islands, including AN and NAN speakers, as well as the relationship between languages and genes, by means of nonrecombining Y-chromosomal (NRY) and mitochondrial DNA (mtDNA) analysis. We found that the eastern Indonesian gene pool consists of East Asian as well as Melanesian components, as might be expected based on linguistic evidence, but also harbors putative indigenous eastern Indonesian signatures that perhaps reflect the initial occupation of the Wallacea by aboriginal hunter-gatherers already in Palaeolithic times. Furthermore, both NRY and mtDNA data showed a complete lack of correlation between linguistic and genetic relationships, most likely reflecting genetic admixture and/or language shift. In addition, we noted a small fraction of the NRY and mtDNA data shared between eastern Indonesians and Australian Aborigines likely reflecting an ancient link between Asia and Australia. Our data thus provide insights into the complex genetic ancestry history of eastern Indonesian islanders characterized by several admixture episodes and demonstrate a clear example of the lack of the often-assumed correlation between the genes and languages of human populations.
Paternal genetic affinity between western Austronesians and Daic populations (2008)
The ISEA populations may also be admixed. In our study, we assumed that the ISEA were mixed by three potential parental populations: Daic populations, Taiwan aborigines, and the indigenous populations of the Sunda Islands, who are similar to Papuans. We performed an admixture analysis on the Indonesians, and included data of the Papuans from the literature [36,37] as one of the parental population structures in the analysis. Our analysis showed the following admixture proportions: Daic (0.713 ± 0.124), Taiwan (0.143 ± 0.125), and Papuans (0.144 ± 0.050), indicating that the contribution of the Daic ancestry on the Indonesians is the most dominant. There is some uncertainty in these data as our assumption that the ISEA population is an admixture can not be tested.
A Mitochondrial Stratigraphy for Island Southeast Asia (2006)
Almost 14% of individuals found in ISEA have mtDNA haplotypes that belong to macrohaplogroup M but that appear unrelated to other M types found outside ISEA and that date to ~40,000–70,000 years ago. It seems likely that these haplotypes, and others found only in the Malay Peninsula, can be traced back to the original inhabitants of ISEA, who would have colonized the area at around that time.73 Haplogroups N21 and R22 may provide further evidence of the persistence of mtDNAs from the earliest settlers. Today, N21 is more common in the aboriginal populations of the Malay Peninsula,35 but the phylogeographic pattern suggests that it arrived there from Sumatra. Haplogroup R22 now appears to be most common in the Shompen group of the Nicobar Islands70; however, it is most diverse in ISEA, and the root type is only found in Lombok and Alor, suggesting that it could be an indigenous marker for that area. If haplogroups N21, R22, M45, M46, M47, and M21d and the remaining unclassified M* types do indeed represent indigenous haplogroups, then this suggests that about a fifth of the modern inhabitants can trace their maternal ancestry back to the first anatomically modern settlers of ISEA.
In this study, the Near Oceanian haplogroups P and Q were found at low levels in ISEA. Haplogroup P is rare and has been found only at low levels in Sulawesi and Sumba. Haplogroup Q is most common in the easternmost locations studied (reaching 29% in Alor, where Papuan as well as Austronesian languages are spoken76), but, at 3% of the sample as a whole, it is found as far west as Borneo, indicating long-range gene flow from Near Oceania into ISEA.
A predominantly indigenous paternal heritage for the Austronesian-speaking peoples of insular Southeast Asia and Oceania. (2001)
Modern humans reached Southeast Asia and Oceania in one of the first dispersals out of Africa. The resulting temporal overlap of modern and archaic humans-and the apparent morphological continuity between them-has led to claims of gene flow between Homo sapiens and H. erectus. Much more recently, an agricultural technology from mainland Asia spread into the region, possibly in association with Austronesian languages. Using detailed genealogical study of Y chromosome variation, we show that the majority of current Austronesian speakers trace their paternal heritage to Pleistocene settlers in the region, as opposed to more-recent agricultural immigrants. A fraction of the paternal heritage, however, appears to be associated with more-recent immigrants from northern populations. We also show that the northern Neolithic component is very unevenly dispersed through the region, with a higher contribution in Southeast Asia and a nearly complete absence in Melanesia. Contrary to claims of gene flow (under regional continuity) between H. erectus and H. sapiens, we found no ancestral Y chromosome lineages in a set of 1,209 samples. The finding excludes the possibility that early hominids contributed significantly to the paternal heritage of the region.
I'll post some studies. But i'm also curious to know what your intuitive guesses might be.
Balinese Y-chromosome perspective on the peopling of Indonesia: genetic contributions from pre-neolithic hunter-gatherers, Austronesian farmers, and Indian traders (2005)
The observed frequencies of K-M9*, K-M230, and M-P34 on Bali suggest that 2.2% of the pre-Neolithic gene pool survived the invasion of AustronesianY chromosomes. Interestingly, a similar extent of replacement is evident in Java(3.8%), and a slightly higher proportion of pre-Neolithic Y chromosomes is ob-served in Borneo (15.0%) (Kayser et al. 2003). A similar analysis of our sample of eastern Indonesians indicates major pre-Neolithic (78.2%) and minor Aus-tronesian (21.8%) components of their paternal gene pool
Philippine mitochondrial DNA diversity: a populated viaduct between Taiwan and Indonesia? (2009)
Relatively little is known about the genetic diversity of the Philippine population, and this is an important gap in our understanding of Southeast Asian and Oceanic prehistory. Here we describe mitochondrial DNA (mtDNA) variation in 423 Philippine samples and analyze them in the context of the genetic diversity of other Southeast Asian populations. The majority of Philippine mtDNA types are shared with Taiwanese aboriginal groups and belong to haplogroups of postglacial and pre-Neolithic origin that have previously been identified in East Asian and Island Southeast Asian populations. Analysis of hypervariable segment I sequence variation within individual mtDNA haplogroups indicates a general decrease in the diversity of the most frequent types (B4a1a, E1a1a, and M7c3c) from the Taiwanese aborigines to the Philippines and Sulawesi, although calculated standard error measures overlap for these populations. This finding, together with the geographical distribution of ancestral and derived haplotypes of the B4a1a subclade including the Polynesian Motif, is consistent with southward dispersal of these lineages "Out of Taiwan" via the Philippines to Near Oceania and Polynesia. In addition to the mtDNA components shared with Taiwanese aborigines, complete sequence analyses revealed a minority of lineages in the Philippines that share their origins--possibly dating back to the Paleolithic--with haplogroups from Indonesia and New Guinea. Other rare lineages in the Philippines have no closely related types yet identified elsewhere
Genetic admixture history of Eastern Indonesia as revealed by Y-chromosome and mitochondrial DNA analysis. (2009)
Eastern Indonesia possesses more linguistic diversity than any other region in Southeast Asia, with both Austronesian (AN) languages that are of East Asian origin, as well as non-Austronesian (NAN) languages of likely Melanesian origin. Here, we investigated the genetic history of human populations from seven eastern Indonesian islands, including AN and NAN speakers, as well as the relationship between languages and genes, by means of nonrecombining Y-chromosomal (NRY) and mitochondrial DNA (mtDNA) analysis. We found that the eastern Indonesian gene pool consists of East Asian as well as Melanesian components, as might be expected based on linguistic evidence, but also harbors putative indigenous eastern Indonesian signatures that perhaps reflect the initial occupation of the Wallacea by aboriginal hunter-gatherers already in Palaeolithic times. Furthermore, both NRY and mtDNA data showed a complete lack of correlation between linguistic and genetic relationships, most likely reflecting genetic admixture and/or language shift. In addition, we noted a small fraction of the NRY and mtDNA data shared between eastern Indonesians and Australian Aborigines likely reflecting an ancient link between Asia and Australia. Our data thus provide insights into the complex genetic ancestry history of eastern Indonesian islanders characterized by several admixture episodes and demonstrate a clear example of the lack of the often-assumed correlation between the genes and languages of human populations.
Paternal genetic affinity between western Austronesians and Daic populations (2008)
The ISEA populations may also be admixed. In our study, we assumed that the ISEA were mixed by three potential parental populations: Daic populations, Taiwan aborigines, and the indigenous populations of the Sunda Islands, who are similar to Papuans. We performed an admixture analysis on the Indonesians, and included data of the Papuans from the literature [36,37] as one of the parental population structures in the analysis. Our analysis showed the following admixture proportions: Daic (0.713 ± 0.124), Taiwan (0.143 ± 0.125), and Papuans (0.144 ± 0.050), indicating that the contribution of the Daic ancestry on the Indonesians is the most dominant. There is some uncertainty in these data as our assumption that the ISEA population is an admixture can not be tested.
A Mitochondrial Stratigraphy for Island Southeast Asia (2006)
Almost 14% of individuals found in ISEA have mtDNA haplotypes that belong to macrohaplogroup M but that appear unrelated to other M types found outside ISEA and that date to ~40,000–70,000 years ago. It seems likely that these haplotypes, and others found only in the Malay Peninsula, can be traced back to the original inhabitants of ISEA, who would have colonized the area at around that time.73 Haplogroups N21 and R22 may provide further evidence of the persistence of mtDNAs from the earliest settlers. Today, N21 is more common in the aboriginal populations of the Malay Peninsula,35 but the phylogeographic pattern suggests that it arrived there from Sumatra. Haplogroup R22 now appears to be most common in the Shompen group of the Nicobar Islands70; however, it is most diverse in ISEA, and the root type is only found in Lombok and Alor, suggesting that it could be an indigenous marker for that area. If haplogroups N21, R22, M45, M46, M47, and M21d and the remaining unclassified M* types do indeed represent indigenous haplogroups, then this suggests that about a fifth of the modern inhabitants can trace their maternal ancestry back to the first anatomically modern settlers of ISEA.
In this study, the Near Oceanian haplogroups P and Q were found at low levels in ISEA. Haplogroup P is rare and has been found only at low levels in Sulawesi and Sumba. Haplogroup Q is most common in the easternmost locations studied (reaching 29% in Alor, where Papuan as well as Austronesian languages are spoken76), but, at 3% of the sample as a whole, it is found as far west as Borneo, indicating long-range gene flow from Near Oceania into ISEA.
A predominantly indigenous paternal heritage for the Austronesian-speaking peoples of insular Southeast Asia and Oceania. (2001)
Modern humans reached Southeast Asia and Oceania in one of the first dispersals out of Africa. The resulting temporal overlap of modern and archaic humans-and the apparent morphological continuity between them-has led to claims of gene flow between Homo sapiens and H. erectus. Much more recently, an agricultural technology from mainland Asia spread into the region, possibly in association with Austronesian languages. Using detailed genealogical study of Y chromosome variation, we show that the majority of current Austronesian speakers trace their paternal heritage to Pleistocene settlers in the region, as opposed to more-recent agricultural immigrants. A fraction of the paternal heritage, however, appears to be associated with more-recent immigrants from northern populations. We also show that the northern Neolithic component is very unevenly dispersed through the region, with a higher contribution in Southeast Asia and a nearly complete absence in Melanesia. Contrary to claims of gene flow (under regional continuity) between H. erectus and H. sapiens, we found no ancestral Y chromosome lineages in a set of 1,209 samples. The finding excludes the possibility that early hominids contributed significantly to the paternal heritage of the region.