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Sexual dimorphism is often observed in Crustaceans. Considering the great diversity of this subphylum, only few reports are found in the literature and most are mainly based on traditional morphometry. The present study uses geometric morphometrics analysis to identify sexual dimorphism by shape variation in the overexploited semiterrestrial crab Ucides cordatus, species with great social and economic importance in South America. Comparative morphology analyses were performed by using the outer face of the propodus of major cheliped, dorsal and anterior region of carapace shape. Significant differences in shape between sexes were detected in these body areas. The causes of dimorphism presented in this species are not clear but, analogous to other possibly associated species, it may be inferred that the causes are with adaptations to body ability of reproductive potential (females), and of reproductive behaviour and agonistics encounters (males). Additional analyses on courtship displays and other reproductive aspects should provide better comprehension of functionality of this morphological differentiation.

Karyotype analyses of the cryptobenthic marine species Ctenogobius boleosoma and C. smaragdus were performed by means of classical and molecular cytogenetics, including physical mapping of the multigene 18S and 5S rDNA families. C. boleosoma has 2n = 44 chromosomes (2 submetacentrics + 42 acrocentrics; FN = 46) with a single chromosome pair each carrying 18S and 5S ribosomal sites; whereas C. smaragdus has 2n = 48 chromosomes (2 submetacentrics + 46 acrocentrics; FN = 50), also with a single pair bearing 18S rDNA, but an extensive increase in the number of GC-rich 5S rDNA sites in 21 chromosome pairs. The highly divergent karyotypes among Ctenogobius species contrast with observations in several other marine fish groups, demonstrating an accelerated rate of chromosomal evolution mediated by both chromosomal rearrangements and the extensive dispersion of 5S rDNA sequences in the genome.

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Fish constitute a paraphyletic and profusely diversified group that has historically puzzled ichthyologists. Hard efforts are necessary to better understand this group, due to its extensive diversity. New species are often identified and it leads to questions about their phylogenetic aspects. Cytogenetics is becoming an important biodiversity-detection tool also used to measure biodiversity evolutionary aspects. Molecular cytogenetics by fluorescence in situ hybridization (FISH) allowed integrating quantitative and qualitative data from DNA sequences and their physical location in chromosomes and genomes. Although there is no intention on presenting a broader review, the current study presents some evidences on the need of integrating molecular cytogenetic data to other evolutionary biology tools to more precisely infer cryptic species detection, population structuring in marine environments, intra- and interspecific karyoevolutionary aspects of freshwater groups, evolutionary dynamics of marine fish chromosomes, and the origin and differentiation of sexual and B chromosomes. The new cytogenetic field, called cytogenomics, is spreading due to its capacity to give resolute answers to countless questions that cannot be answered by traditional methodologies. Indeed, the association between chromosomal markers and DNA sequencing as well as between biological diversity analysis methodologies and phylogenetics triggers the will to search for answers about fish evolutionary, taxonomic, and structural features.

The taxonomic status of Pomacentridae species can be difficult to determine, due to the high diversity, and in some cases, poorly understood characters, such as color patterns. Although Stegastes rocasensis, endemic to the Rocas atoll and Fernando de Noronha archipelago, and S. sanctipauli, endemic to the São Pedro and São Paulo archipelago, differ in color pattern, they exhibit similar morphological characters and largely overlapping counts of fin rays and lateral-line scales. Another nominal insular species, S. trindadensis, has recently been synonymized with S. fuscus but retained as a valid subspecies by some authors. Counts and morphometric analyses and mitochondrial DNA (COI, 16SrRNA, CytB) and nuclear DNA (rag1 and rhodopsin) comparisons of three insular species (S. rocasensis, S. sanctipauli and S. trindadensis) and three other South Atlantic species (S. fuscus, S. variabilis and S. pictus) were carried out in the present study. Analyses of the principal components obtained by traditional multivariate morphometry indicate that the species in general have similar body morphology. Molecular analyses revealed conspicuous similarity between S. rocasensis and S. sanctipauli and between S. trindadensis and S. fuscus and a clear divergence between S. variabilis from Northeast Brazil and S. variabilis from the Caribbean region. Our data suggest that S. sanctipauli is a synonym of S. rocasensis, support the synonymy of S. trindadensis with S. fuscus, and reveal the presence of a likely cryptic species in the Caribbean that has been confused historically with S. variabilis.

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