Summary: It is widely recognized that macroecological patterns are not independent of the evolution of the lineages involved in generating these patterns. While many researchers have begun to evaluate the effect of ancestor–descendant relationships on observed patterns using the phylogenetic comparative method, most macroecological studies only utilize the cross‐sectional comparative method to ‘remove the phylogenetic history’, without considering the option of evaluating its effect without removing it. Currently, most researchers use this method without explicitly evaluating three fundamental evolutionary assumptions of the comparative method: (i) that the phylogeny is constructed without error (which implies evaluating phylogenetic uncertainty); (ii) that more closely related species tend to show more similar characters than expected by chance (which implies evaluating the phylogenetic signal) and; (iii) that the model of the characters' evolution effectively recapitulates their history (which implies comparing the fit of several evolutionary models and evaluating the uncertainty of the estimating model parameters). Macroecological studies will benefit from the use of the comparative method to assess the effect of phylogenetic history without removing its effect. The comparative method will also allow for the simultaneous analysis of trait evolution and its impact on diversification rates; it is important to evaluate these processes together because they are not independent. In addition, explicit evaluations of the assumptions of comparative methods using Bayesian inferences will allow researchers to quantify the uncertainty of specific evolutionary hypotheses accounting for observed macroecological patterns. We illustrate the usefulness of the method using the phylogeny of the genusSebastes(Pisces: Scorpaeniformes), together with data on the body size–latitudinal range relationship to estimate the effect of phylogenetic history on the observed macroecological pattern.

The genetic structure of present-day populations has been highly affected by glacial periods and physical oceanographic forcing, particularly with respect to species distributions and population gene-flow patterns. We assessed the current genetic composition of the Jasus frontalis population in the southeastern Pacific Islands off the coast of Chile to evaluate their connectivity modulated by contemporary and historic oceanographic processes. Population structure and demographical history for this species were assessed based on classic and Bayesian approaches using 84 sequences of cytochrome oxidase subunit I. In addition, we estimated the time of origin of J. frontalis in the different geographic zones. The analyses show a panmictic population with high gene flow between subcomponents and a lack of genetic structure (F_ST < 0.008). This high gene flow is mainly modulated by mesoscale oceanographic factors such as eddies and meanders. In a historical spatial context, the most probable common ancestor of J. frontalis could have colonized the region around 0.258 million years before present (MYBP), first becoming established in the Juan Fernández Archipelago and then expanding toward the Desventuradas Islands. The demographic history shows a consistent increase in the effective population size (N_e) starting approximately 0.130 MYBP, which is highly correlated with sea-level changes during the last glacial maximum.

Previous studies of population genetic structure inDissostichus eleginoideshave shown that oceanographic and geographic discontinuities drive in this species population differentiation. Studies have focused on the genetics ofD.eleginoidesin the Southern Ocean; however, there is little knowledge of their genetic variation along the South American continental shelf. In this study, we used a panel of six microsatellites to test whetherD.eleginoidesshows population genetic structuring in this region. We hypothesized that this species would show zero or very limited genetic structuring due to the habitat continuity along the South American shelf from Peru in the Pacific Ocean to the Falkland Islands in the Atlantic Ocean. We used Bayesian and traditional analyses to evaluate population genetic structure, and we estimated the number of putative migrants and effective population size. Consistent with our predictions, our results showed no significant genetic structuring among populations of the South American continental shelf but supported two significant and well-defined genetic clusters ofD.eleginoidesbetween regions (South American continental shelf and South Georgia clusters). Genetic connectivity between these two clusters was 11.3% of putative migrants from the South American cluster to the South Georgia Island and 0.7% in the opposite direction. Effective population size was higher in locations from the South American continental shelf as compared with the South Georgia Island. Overall, our results support that the continuity of the deep-sea habitat along the continental shelf and the biological features of the study species are plausible drivers of intraspecific population genetic structuring across the distribution ofD.eleginoideson the South American continental shelf.

Insects in many species vary greatly in the expression of secondary sexual traits, resulting in sexual dimorphism, which has been proposed to be a consequence of differences in sexual selection. In this study, we analyze the occurrence of sexual shape dimorphism and the correlation between geometric body size in males and females and sex ratio in the genus Ceroglossus (Coleoptera: Carabidae) using geometric morphometrics and randomization analysis. Our results show a positive relationship between the centroid size of males and females and sex ratio. However, we also observed a trend to maintain a "similar" body shape between sexes and species due to characteristics associated with sexual selection of the group in which the scarcity of outstanding morphological characters does not restrict reproduction capacity. The trend in sexual proportions was found to be near 1:1 for the eight species. We propose that the observed differences between sexes associated with the sex ratio are due to an energy cost caused by sexual selection; nevertheless, since proportions are similar for all the species, it is really not relevant to generate more conspicuous structures for a stronger male-male competence.

Although the degree of mate competition, given extreme differences in sex ratio, explains much of the pattern of male-biased size dimorphism among diverse taxa, it fails for some species which have potential for intense male competition for mates and yet exhibit little or no sexual size dimorphism (SSD). This fact suggest that species with low SSD should be express the effect of evolutionary pressure in non-obvious geometrical shape promoted by sex ratio in an evolutionary time scale. To evaluate this hypothesis we used phylogenetic comparative method in a Bayesian framework to investigate the evolution of SSD and the role of sex ratio at inter-specific level in the species of Ceroglossus (Coleoptera: Carabidae). In our results the proportion farthest from 1:1 is associated with more disparate body shape, even though the entire group has minimum variation in sex ratio, which is an intrinsic life history character of this group considering its phylogenetic conservatism or phylogenetic signal. We suggest that the sex ratio has determined the dimorphism degree during evolution of this group, since both traits have increased or decreased together during the species divergence (i.e. positive phylogenetic correlation: r²≈0.85). We suggest that morphological studies of SSD will benefit from using comparative method with Bayesian approaches to assess the effect of phylogenetic history and its uncertainty. Finally, this will be allow to researchers to quantify the uncertainty of specific evolutionary hypotheses accounting for observed sexual dimorphism patterns.