Molecular phylogenetics of the white-lipped peccary (Tayassu pecari) did not confirm morphological subspecies in northwestern South America.

We sequenced the mitochondrial DNA (mtDNA) control region of 59 peccaries (44 white-lipped peccaries, Tayassu pecari, and 15 collared peccaries, Pecari tajacu). We also genotyped 3 DNA microsatellites from 78 white-lipped peccaries representing the 4 putative morphological subspecies (i.e., spiradens, aequatoris, pecari, and albirostris) present in northwestern South America (i.e., Colombia, Ecuador, Peru, and Bolivia). Our results showed: 1) the estimated diversity of the mtDNA control region in the T. pecari population was extremely high, whereas the average genetic diversity for the microsatellites was medium to high and similar to that observed in European pig breeds; 2) there was no significant genetic heterogeneity among the quoted putative morphological subspecies at the mitochondrial marker, but we did detect significant (although relatively small) genetic heterogeneity using microsatellites, indicating that T. pecari albirostris is a uniquely differentiated group; and 3) the phylogenetic mtDNA trees showed that haplotypes were intermixed independent of their "a priori" subspecies classification. In addition, the microsatellite assignation analyses yielded low percentages of well-classified individuals when the analysis considered the geographic morphology of the subspecies. Thus, the molecular results do not support the putative morphological subspecies of T. pecari in northwestern South America. Finally, our results did not detect clear historical demographic changes using the mtDNA control region sequences. These genetic results are discussed in the context of the ecological and social characteristics of T. pecari.

Molecular phylogenetics and phylogeography of the white-fronted capuchin (Cebus albifrons; Cebidae, Primates) by means of mtCOII gene sequences.

A total of 696 base pairs (bp) of the mitochondrial COII gene were sequenced from 118 individuals of Cebus albifrons (plus an individual of Cebus olivaceus) sampled from diverse geographical areas of Colombia, Peru, Ecuador and Brazil. These animals represented all of the C. albifrons's taxa described by Hershkovitz (1949) in Colombia and Peru (10 out of 13 subspecies are described by this author). The sequences analyzed demonstrate the existence of three well defined groups in northern Colombia (trans-Andean): malitosus, versicolor-pleei-cesarae and leucocephalus. They arose from at least, three distinct migrations from different Amazonian groups. Five different Amazonian and Eastern Llanos C. albifrons's groups (I, II, III, IV, and V) were also found. In many Amazonian localities, some of these groups live in sympatry probably by secondary expansion after their respective formations. Amazonian group I is closely related to the versicolor-pleei-cesarae group, malitosus is closely related to Amazonian group V, while leucocephalus is closely related to Amazonian group IV. Nevertheless, our genetic analysis could not resolve the genetic relationships among the main C. albifrons groups. The ρ-statistic applied to the median-joining network yielded that the major part of the temporal splits estimated occurred in the Pleistocene, reinforcing the importance of the Pleistocene refugia during the evolution of C. albifrons.