Molecular Identification and Traceability of Illegal Trading in Lignobrycon myersi

Lignobrycon myersi is a threatened freshwater fish species and endemic of a few coastal rivers in northeastern Brazil. Even though the Brazilian laws prohibit the fisheries of threatened species, L. myersi is occasionally found in street markets, being highly appreciated by local population. In order to provide a reliable DNA barcode dataset for L. myersi, we compared mitochondrial sequences of cytochrome c oxidase subunit I (COI) from fresh, frozen, and salt-preserved specimens. Phylogenetically related species (Triportheus spp.) and other fish species (Astyanax fasciatus) commonly mixed with L. myersi in street markets were also included to test the efficiency of molecular identification. In spite of the differences in conservation processes and advanced deterioration of some commercial samples, high-quality COI sequences were obtained and effective in discriminating L. myersi specimens. In addition, while populations from Contas and Almada River basins seem to comprise a single evolutionary lineage, the specimens from Cachoeira River were genetically differentiated, indicating population structuring. Therefore, DNA barcoding has proved to be useful to trace the illegal trading of L. myersi and to manage threatened populations, which should focus on conservation of distinct genetic stocks and mitigation on human impacts along their range

Cytogenetic analysis in Tetragonopterus franciscoensis (Characiformes): another piece to the karyoevolutionary puzzle of tetra fishes

Tetragonopterus is a taxonomically complex genus in Characidae, being currently represented by nine species according to integrative approaches. One of them, T. franciscoensis was recently validated in rivers from northeastern Brazil. Even though molecular and morphological data have been collected in Tetragonopterus, the cytogenetic analyses in this group are scarce despite of the role of chromosomal variation in speciation. Herein, we present the first detailed karyotypic study in T. franciscoensis along with a comparative analysis with published cytogenetic data in characin fish. All specimens shared 2n=52 distributed in 12 metacentric (m), 12 submetacentric (sm), and 28 subtelocentric/acrocentric (st/a) chromosomes for both sexes as well as single nucleolus organizer regions on short arms of pair 8 and several GC-rich sites. The mapping of telomeric sequences (TTAGGG)n revealed no telomeric interstitial signals. While subtle cytogenetic differences were observed between samples from northeastern basins in Brazil, corroborating a recent genetic divergence, distinct karyotypes were detected in relation to congeneric taxa from other Brazilian regions. Therefore, the origin of large biarmed pairs in species with low 2n values should be related to occurrence of centric fusions

Identification of distinct evolutionary units in allopatric populations of Hypostomus cf. wuchereri Günther, 1864 (Siluriformes: Loricariidae): karyotypic evidence

Few chromosomal reports are available for the endemic fish fauna from coastal basins in northeastern Brazil, and regional biodiversity remains partially or completely unknown. This is particularly true for Loricariidae, the most diverse family of armored catfishes. In the present work, allopatric populations of Hypostomus cf. wuchereri (Siluriformes: Loricariidae) from two basins in Bahia (northeastern Brazil) were cytogenetically analyzed. Both populations shared 2n = 76 chromosomes, a karyotype formula of 10m+18sm+48st/a (FN = 104) and single terminal GC-rich NORs on the second metacentric pair. Nevertheless, microstructural differences were detected by C-banding, fluorochrome staining and chromosomal digestion with restriction enzymes (Alu I, Bam HI, Hae III, and Dde I). The population from Una River (Recôncavo Sul basin) showed conspicuous heterochromatin blocks and a remarkable heterogeneity of base composition (presence of interspersed AT/GC-rich and exclusively AT- or GC-rich sites), while the population from Mutum river (Contas River basin) presented interstitial AT-rich C-bands and terminal GC/AT-rich heterochromatin. Each enzyme yielded a specific band profile per population which allowed us characterizing up to five heterochromatin families in each population. Based on the present data, we infer that these populations have been evolving independently, as favored by their geographic isolation, probably representing cryptic species