No abstract

Cytogenetic analysis was performed in six nominal taxa of the genus Ctenomys with a diploid number of 2n=47/48. The studied species were: C. australis (2n=48, FN=76); C. mendocinus (2n=47/48, FN=68/75/76); C. porteousi (2n=47/48, FN=71/72/73); C. azarae (2n=47, FN=71); C. sp. ('chasiquensis') (2n=47/48); and C. talarum (2n=48, FN=80). The first three species shared the whole complement, C. talarum shares with them 19 arms from a total of 43 (44%). In all species analyzed constitutive heterochromatin was detected in most short arms, and in several centromeres. Polymorphisms for several pairs involving the heterochromatic short arms together with a complex polymorphism of pair A 1 were found in C. azarae, C. sp., C. mendocinus and C. porteousi. Intraindividual variation found in one specimen of C. porteousi involving heterochromatic arms is discussed.These results lead us to propose the inclusion of all species except C. talarum, within a complex called the mendocinus-group. A new case of conservatism for chromosomal number in the genus Ctenomys is found in this group.

The chromosomal distribution of the major satellite DNA of South American rodents of the genus Ctenomys was analyzed in eight species by in situ hybridization, using a probe isolated from C porteousi. The hybridization patterns showed different numbers of chromosomes with positive pericentromeric regions and/or complete short arms. In some species, a positive signal was scarce (or not detectable, as in C. opimus), and was usually located in the pericentromeric areas (C. occultus and C latro). In those species where the satellite was highly amplified, its chromosomal localization tended to encompass the entire length of the short arms. These patterns were compared with C-band distribution patterns in the same species. We discuss the putative evolutionary trend of this satellite DNA in the genus Ctenomys and suggest that it evolved from a strictly pericentromeric localization to comprising the whole short arms of some chromosomes.

We present new cytogenetic, morphometric, and sperm morphology data of eight populations belonging to the C. pundti complex from Southern Córdoba and Eastern La Pampa Provinces in Argentina. The diploid numbers ranged from 2n = 44 to 2n = 50, and C- bands revealed a pattern of centromeric and pericentromeric heterochromatin. Comparisons of G-banded karyotypes revealed that the 2n = 44 (Holmberg, Santa Catalina, Sampacho), 2n = 46 (Realicó), 2n = 48 (El Guanaco, Guatraché), 2n = 46-48 (Vicuña Mackenna), and 2n = 50 (Puente Olmos) karyotypes, are closely related. In addition, these karyotypes show a high degree of homology (95%) with C. talarum talarum, despite the fact that five chromosomal rearrangements differentiate both taxa. Discriminant Function Analysis of morphometric data allows to distinguish three clusters: i) the C. mendocinus species group, ii) C. t. talarum, and iii) populations of the C. pundti complex proposed herein. The close phylogenetic relationship between C. talarum and the C. pundti complex, which undoubtedly belong to the same evolutionary lineage, is well supported by two different kinds of evidence: the extensive chromosomal homology and the same symmetric type of sperm. The morphological and chromosomal differences show that these two forms have diverged recently.