Comparative cytogenetic analysis in the species Uroderma magnirostrum and U. bilobatum (cytotype 2n = 42) (Phyllostomidae, Stenodermatinae) in the Brazilian Amazon

The genus Uroderma includes two species: U. magnirostrum and U. bilobatum. These species are characterized by their high degree of karyotypic evolution, diverging from most other species of the subfamily Stenodermatinae, which have a lower degree of chromosomic evolution. The present study reports the first banding patterns of U. magnirostrum (G-, C-banding and Ag-NOR) and U. bilobatum (C-banding and Ag-NOR). The chromosomic data in conventional staining of U. magnirostrum (2n = 36, NF = 62) and U. bilobatum (cytotype 2n = 42, NF = 50) are equivalent to that described in the literature. When compared, chromosomal homeologies are found in both karyotypes, as well as differences, confirming that karyotypic evolution in the Uroderma genus is intense. Fission, fusion, inversion or translocation events are required to explain the karyotypic evolution of this genus. The comparison of karyotype, described here, to one of the species of the genus Artibeus (2n = 30/31), suggests that some chromosomic forms are apomorphic and shared between the two species of Uroderma. This confirms the monophyly of the enus, and that U. magnirostrum presents a more primitive karyotype when compared to U. bilobatum

Comparative morphology of the first zoea of twelve brachyuran species (Crustacea: Decapoda) from the Amazon region

The laboratory-hatched first zoeal stage of twelve brachyuran species collected in the estuarine area of the Caeté River in the Amazonian region are described and illustrated in the present study: P. americanus Saussure, 1857, Eurytium limosum (Say, 1818), Sesarma curacaoense De Man, 1892, S. rectum Randall, 1840, Armases rubripes (Rathbun, 1897), Aratus pisonii (H. Milne Edwards, 1837), Ocypode quadrata (Fabricius, 1787), Uca rapax (Smith, 1870), U. maracoani (Latreille, 1802), U. thayeri Rathbun, 1900, Ucides cordatus (Linnaeus, 1763) and Pachygrapsus gracilis (Saussure, 1858). Through intraspecific comparisons of the respective larval stage, an identification key was generated and provided. Most of the studied species presented morphological differences (e.g. type and presence or absence of setae) when compared to the same species previously described in the literature.

Chromosomal diversity in three species of electric fish (Apteronotidae, Gymnotiformes) from the Amazon Basin

Cytogenetic studies were carried out on samples of Parapteronotus hasemani, Sternarchogiton preto and Sternarchorhamphus muelleri (Apteronotidae, Gymnotiformes) from the Amazon basin. The first two species exhibited both a 2n = 52 karyotype, but differed in their karyotypic formulae, distribution of constitutive heterochromatin, and chromosomal location of the NOR. The third species, Sternarchorhamphus muelleri, was found to have a 2n = 32 karyotype. In all three species the DAPI and chromomycin A3 staining results were consistent with the C-banding results and nucleolar organizer region (NOR) localization. The 18S rDNA probe confirmed that there was only one pair of ribosomal DNA cistron bearers per species. The telomeric probe did not reveal interstitial telomeric sequences (ITS). The karyotypic differences among these species can be used for taxonomic identification. These data will be useful in future studies of these fishes and help understanding the phylogenetic relationships and chromosomal evolution of the Apteronotidae.