Experimental evolution on heat tolerance and thermal performance curves under contrasting thermal selection in Drosophila subobscura.

Ectotherms can respond to global warming via evolutionary change of their upper thermal limits (CTmax ). Thus, the estimation of CTmax and its evolutionary potential is crucial to determine their vulnerability to global warming. However, CTmax estimations depend on the thermal stress intensity, and it is not completely clear whether its evolutionary capacity can be affected. Here, we performed an artificial selection experiment to increase heat tolerance using fast- and slow-ramping selection protocols in Drosophila subobscura. We found that heat tolerance evolved in both selection protocols, exhibiting similar evolutionary change rates and realized heritabilities. Additionally, we estimated the thermal performance curves (TPC) to evaluate correlated responses to selection on heat tolerance. We detected that thermal optimum increased in fast-ramping selection lines, but with a cost at the thermal performance breadth. Conversely, we did not detect changes in the TPC for the slow-ramping selection lines, indicating that thermal stress intensity has important effects on the evolution of thermal physiology of ectotherms. These findings, together with previous studies in D. subobscura reporting interpopulation variability and significant heritabilities for heat tolerance, suggest that evolutionary change can contribute to insect persistence in thermally changing environments and adaptation to global warming conditions.

The reproductive period of tarantulas is constrained by their thermal preferences (Araneae, Theraphosidae).

Locomotor and physiological performance of ectotherms are affected by temperature. Thermoregulation is achieved by changes in behavior and the selection of micro-habitats with adequate temperatures to maintain the body temperature (Tb) within a range of preference. Apart from this temperature dependence at spatial scales, ectotherms are also affected by temperature at temporal scale. For instance, ectotherms can only be active some months of the year, particularly in temperate environments. Tarantulas are ectotherms that live in burrows most of their life. Nevertheless, after the sexual maturation molt, males leave their refugia and start a wandering life searching for females to mate. The reproductive period varies among species. In some species walking males are seen in late spring or early summer, while in other species males are only seen during fall or winter. Apart from the differences in lifestyles after maturation, tarantulas exhibit sexual dimorphisms in longevity and body mass, having smaller, shorter-lived males. Thus, to optimize energetic budgets, decreasing thermoregulation costs, we hypothesize and examine a putative correlation between an individual's preferred body temperature (Tpref) and the environmental temperature during the reproductive period. Hence, we characterize Tpref in seven tarantula species and analyze which factors (i.e., time of day, body mass, and sex) correlated with it. Furthermore, we assess putative correlated evolution of Tpref with ambient temperature (minima, mean, and maxima) during the reproductive period by means of phylogenetic independent contrasts. We did not find differences in thermal preferences between sexes; and only one species, Acanthoscurria suina, exhibited diel differences in Tpref. We found evidence of correlated evolution between Tpref and minimum temperature during the reproductive period among all seven species studied herein. Our results show that the reproductive period is constrained by thermal preferences, dictating when males can start their wandering life to mate.

Male-male competition and repeated evolution of terrestrial breeding in Atlantic Coastal Forest frogs.

Terrestrial breeding is a derived condition in frogs, with multiple transitions from an aquatic ancestor. Shifts in reproductive mode often involve changes in habitat use, and these are typically associated with diversification in body plans, with repeated transitions imposing similar selective pressures. We examine the diversification of reproductive modes, male and female body sizes, and sexual size dimorphism (SSD) in the Neotropical frog genera Cycloramphus and Zachaenus, both endemic to the Atlantic rainforest of Brazil. Species in this clade either breed in rocky streams (saxicolous) or in terrestrial environments, allowing us to investigate reproductive habitat shifts. We constructed a multilocus molecular phylogeny and inferred evolutionary histories of reproductive habitats, body sizes, and SSD. The common ancestor was small, saxicolous, and had low SSD. Terrestrial breeding evolved independently three times and we found a significant association between reproductive habitat and SSD, with shifts to terrestrial breeding evolving in correlation with decreases in male body size, but not female body size. Terrestrial breeding increases the availability of breeding sites and results in concealment of amplexus, egg-laying, and parental care, therefore reducing male-male competition at all stages of reproduction. We conclude that correlated evolution of terrestrial reproduction and small males is due to release from intense male-male competition that is typical of exposed saxicolous breeding.

Testing the Domino Theory of Gene Loss in Buchnera aphidicola: The Relevance of Epistatic Interactions.

The domino theory of gene loss states that when some particular gene loses its function and cripples a cellular function, selection will relax in all functionally related genes, which may allow for the non-functionalization and loss of these genes. Here we study the role of epistasis in determining the pattern of gene losses in a set of genes participating in cell envelope biogenesis in the endosymbiotic bacteria Buchnera aphidicola. We provide statistical evidence indicating pairs of genes in B. aphidicola showing correlated gene loss tend to have orthologs in Escherichia coli known to have alleviating epistasis. In contrast, pairs of genes in B. aphidicola not showing correlated gene loss tend to have orthologs in E. coli known to have aggravating epistasis. These results suggest that during the process of genome reduction in B. aphidicola by gene loss, positive or alleviating epistasis facilitates correlated gene losses while negative or aggravating epistasis impairs correlated gene losses. We interpret this as evidence that the reduced proteome of B. aphidicola contains less pathway redundancy and more compensatory interactions, mimicking the situation of E. coli when grown under environmental constrains.

Expensive Brains: "Brainy" Rodents have Higher Metabolic Rate.

Brains are the centers of the nervous system of animals, controlling the organ systems of the body and coordinating responses to changes in the ecological and social environment. The evolution of traits that correlate with cognitive ability, such as relative brain size is thus of broad interest. Brain mass relative to body mass (BM) varies among mammals, and diverse factors have been proposed to explain this variation. A recent study provided evidence that energetics play an important role in brain evolution (Isler and van Schaik, 2006). Using composite phylogenies and data drawn from multiple sources, these authors showed that basal metabolic rate (BMR) correlates with brain mass across mammals. However, no such relationship was found within rodents. Here we re-examined the relationship between BMR and brain mass within Rodentia using a novel species-level phylogeny. Our results are sensitive to parameter evaluation; in particular how species mass is estimated. We detect no pattern when applying an approach used by previous studies, where each species BM is represented by two different numbers, one being the individual that happened to be used for BMR estimates of that species. However, this approach may compromise the analysis. When using a single value of BM for each species, whether representing a single individual, or available species mean, our findings provide evidence that brain mass (independent of BM) and BMR are correlated. These findings are thus consistent with the hypothesis that large brains evolve when the payoff for increased brain mass is greater than the energetic cost they incur.