To investigate which aspects of contemporary human Y-chromosome variation in Europe are characteristic of primary colonization, late-glacial expansions from refuge areas, Neolithic dispersals, or more recent events of gene flow, we have analyzed, in detail, haplogroup I (Hg I), the only major clade of the Y phylogeny that is widespread over Europe but virtually absent elsewhere. The analysis of 1,104 Hg I Y chromosomes, which were identified in the survey of 7,574 males from 60 population samples, revealed several subclades with distinct geographic distributions. Subclade I1a accounts for most of Hg I in Scandinavia, with a rapidly decreasing frequency toward both the East European Plain and the Atlantic fringe, but microsatellite diversity reveals that France could be the source region of the early spread of both I1a and the less common I1c. Also, I1b*, which extends from the eastern Adriatic to eastern Europe and declines noticeably toward the southern Balkans and abruptly toward the periphery of northern Italy, probably diffused after the Last Glacial Maximum from a homeland in eastern Europe or the Balkans. In contrast, I1b2 most likely arose in southern France/Iberia. Similarly to the other subclades, it underwent a postglacial expansion and marked the human colonization of Sardinia approximately 9,000 years ago.
In a field study of three groups of wild long-tailed macaques, Macaca fascicularis, observations on social behaviour could be related to genetically determined paternity. In contrast to what has been found in many previous studies on captive primate groups, we found a relatively strong correlation between male dominance rank and reproductive success. In a large group the high success of the alpha male compared to other males could be explained only partly by his higher copulation score. His success also resulted partly from better timing of his copulations during maximum fertility of the females, in comparison with other males. We must conclude either that the alpha-male has more access to fertile females, or that females have a preference for the alpha-male during their maximum fertility. The females clearly displayed promiscuous behaviour. This behaviour implies a risk to a female that a male other than the alpha-male with proven qualities will become the father of her offspring. One expects that there must be a social advantage related to this female strategy. In the absence of indications of any direct social advantages to the female of this sexual behaviour pattern, the ultimate explanation for this female promiscuity is most likely is aggression reduction. This could be either through the devaluating of any single copulation, or through the confusion of paternity and a resultant reduction in the risk of infanticide.
A pilot field study was conducted in Sulawesi (Indonesia) to assess the status of macaque populations on the island. Wild and captive animals were sampled, mainly in border areas between presumed different species. The five species investigated were Macaca maurus, M . tonkeana, M . hecki, M . nigrescens, and M . nigra, for which morphological and gene frequency data suggested the presence of hybridization zones. Some individuals within these zones showed intermediate or mosaic morphology between parental forms. These individuals also had intermediate gene frequencies for most of the polymorphic systems investigated. Karyotypes were identical in all species, and no cytogenetic barrier to hybridization existed between species. A review of the recent literature also provided evidence for hybridization between Sulawesi macaques. Clinical frequencies in both morphological and biomolecular traits perhaps can be best explained by the operation of gene flow between the various forms of macaques on the island. However, additional data are necessary before current classification schemes are revised. The unique opportunity and need of further study of Sulawesi macaques for a range of evolutionary questions is emphasized.
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