The Zuni Indians of west‐central New Mexico have been relatively isolated since their foundation by an amalgamation of individuals from different southwestern cultural areas during the Regressive Pueblo period (c.1200–1350 A.D.). Genetic analysis revealed a high frequency of blood type B in both young (0.06) and old (0.05) Zuni, but at 14 other blood group and serum protein loci, allelic frequencies including A (0.011) and Rh negative (0.001) were generally similar to those of other relatively unmixed southwestern Indian tribes. Consideration of Zuni history and demography since Spanish contact in 1540, together with genetic analyses, suggest that the high B frequency probably derives from intermixture with a small number of B, Rh positive non‐Indians in the early post contact period. Genetic differentiation among four southwestern tribes, Zuni, Pima, Papago and Maricopa, was summarized by kinship analysis. Approximately 70% of the inter‐tribal genetic variation could be explained by the geographic distances among these groups showing that isolation by distance has been the most important factor in determining the pattern of regional genetic differentiation.
Genetic studies of 540 Paraguayan Indians from nine tribal groups and 51 Mennonites are presented for ABO, MNSs, P1, Rh, Kell, Lewis, Duffy, Diego; for serum immunoglobulins and haptoglobins, G6PD‐deficiency, and thalassemia trait. Group O gene frequencies for all Indian groups were 1.00; for r (cde), 0.00. Tapiete, Lengua, Toba, and Sanapana Rz (CDE) frequencies were among the highest ever reported. N frequencies were high for Ache Kwera (Guayaki), Lengua, Cheroti, Guarayu, Tapiete; N and s low for Ayore. MS frequencies were high for Sanapana, Lengua, Ayore; Ns for Tapiete. Diego was notably absent for Toba, Lengua, Guarayu, Tapiete, Ayore. Homogeneous frequencies for Fya (1.000) occurred among Guarayu and Tapiete, and for P1 among Guayaki. Inv(a) frequencies were low for Cheroti, Chulupi, Guayaki. Hp 1 among Guayaki (Ache Kwera 0.15) is lowest ever reported. G6PD deficiency and abnormal hemoglobins were uniformly absent from all groups. Mennonite results were homogeneous and point toward Dutch origins. Differences among groups studied, and between Paraguayan and other Amerinds emphasize importance of genetic drift and founder principle. Abandonment of their tribes by mixed‐blood offspring is partly responsible for apparent genetic purity and homogeneity of groups.
Red cell antigen, serum protein and red cell enzyme groups were determined for a series of 1,821 individuals belonging to six language families in Western New Guinea. Three of the language families represent groupings of languages spoken by people in the swampy coastal plain of south central Western New Guinea, two belong to the Central Highlands and one to the Lake Plain area near the confluence of the Idenburg and Rouffaer Rivers.The distribution of genetic markers reveals similarities with other parts of New Guinea. The A2 allele is absent in the ABO system, the frequency of Ns in the MNS system is very high as is the R, (CDe) allele in the Rh system. Hp' frequencies are high, and the transferrin allele T p l is present as in other parts of New Guinea. In the red cell enzyme systems several alleles were detected which are characteristic of Papuan, and in some cases other Melanesian populations: these include MDH3, E K 4 , PGF, PGM% PGMAO, as well as some very restricted alleles such as Peptidue B6 and Pep B 2 .Three indices of genetic distance were computed. The most striking results are the genetic closeness of the Dani and Moni populations from the Central Highlands to the Asmat on the southern coastal plain, and the relative remoteness of the Awyu from the other south coastal populations. The results are discussed in terms of recent theories on the origin and dispersal of Papuan languages.
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