Rapid climate change is likely to impose strong selection pressures on traits important for fitness, and therefore, microevolution in response to climate-mediated selection is potentially an important mechanism mitigating negative consequences of climate change. We reviewed the empirical evidence for recent microevolutionary responses to climate change in longitudinal studies emphasizing the following three perspectives emerging from the published data. First, although signatures of climate change are clearly visible in many ecological processes, similar examples of microevolutionary responses in literature are in fact very rare. Second, the quality of evidence for microevolutionary responses to climate change is far from satisfactory as the documented responses are often - if not typically - based on nongenetic data. We reinforce the view that it is as important to make the distinction between genetic (evolutionary) and phenotypic (includes a nongenetic, plastic component) responses clear, as it is to understand the relative roles of plasticity and genetics in adaptation to climate change. Third, in order to illustrate the difficulties and their potential ubiquity in detection of microevolution in response to natural selection, we reviewed the quantitative genetic studies on microevolutionary responses to natural selection in the context of long-term studies of vertebrates. The available evidence points to the overall conclusion that many responses perceived as adaptations to changing environmental conditions could be environmentally induced plastic responses rather than microevolutionary adaptations. Hence, clear-cut evidence indicating a significant role for evolutionary adaptation to ongoing climate warming is conspicuously scarce.

Comparative analyses of survival senescence by using life tables have identified generalizations including the observation that mammals senesce faster than similar-sized birds. These generalizations have been challenged because of limitations of life-table approaches and the growing appreciation that senescence is more than an increasing probability of death. Without using life tables, we examine senescence rates in annual individual fitness using 20 individual-based data sets of terrestrial vertebrates with contrasting life histories and body size. We find that senescence is widespread in the wild and equally likely to occur in survival and reproduction. Additionally, mammals senesce faster than birds because they have a faster life history for a given body size. By allowing us to disentangle the effects of two major fitness components our methods allow an assessment of the robustness of the prevalent life-table approach. Focusing on one aspect of life history - survival or recruitment - can provide reliable information on overall senescence.

Ecological responses to on-going climate change are numerous, diverse, and taxonomically widespread. However, with one exception, the relative roles of phenotypic plasticity and microevolution as mechanisms in explaining these responses are largely unknown. Several recent studies have uncovered evidence for temporal declines in mean body sizes of birds and mammals, and these responses have been interpreted as evidence for microevolution in the context of Bergmann's rule-an ecogeographic rule predicting an inverse correlation between temperature and mean body size in endothermic animals. We used a dataset of individually marked red-billed gulls (Larus novaehollandiae scopulinus) from New Zealand to document phenotypic and genetic changes in mean body mass over a 47-year (1958 -2004) period. We found that, whereas the mean body mass had decreased over time as ambient temperatures increased, analyses of breeding values estimated with an ''animal model'' approach showed no evidence for any genetic change. These results indicate that the frequently observed climate-change-related responses in mean body size of animal populations might be due to phenotypic plasticity, rather than to genetic microevolutionary responses. adaptation ͉ animal model ͉ quantitative genetics O ne of the major challenges faced by conservation and evolutionary biologists is to understand the role of microevolution in the population responses to the rapid, ongoing global change (1). Evidence for phenotypic responses to global warming is numerous, diverse, and taxonomically widespread (2-5). Examples include advances in phenology (2, 6, 7), poleward shifts in distribution ranges (4,8), and changes in population mean phenotypes such as body size (9). Although adaptation to climate change is often evoked to explain phenotypic time trends (e.g., refs. 7, 10, and 11), the available evidence for evolutionary responses sensu stricto is still scarce (refs. 12, 13; but see refs. 14-16).A large number of correlative studies have found evidence for declines in mean body size of birds (10, 11) and mammals (17-19) over time. These results have been interpreted as evidence for animal adaptation to a warming climate in the framework of Bergmann's rule. The original formulation of the Bergmann's rule applies to geographic variation (20) and predicts an increasing mean body size with increasing latitude as an energetic adaptation to a colder environment. This is because large body size reduces the surface-to-volume ratio and thereby the loss of energy due to conduction. By inference, Bergmann's rule predicts a decreased body size as an adaptive, genetically based response to global warming (9). However, no study has examined whether there is a genetic basis for this interpretation. The decrease in mean body size in a population can also occur as a plastic response to changes in environmental conditions, such as changes in food abundance, food quality, or prevalence of parasites. Hence, decreased mean body size over time might not represent adaptation to global...

Individual multilocus heterozygosity estimates based on a limited number of loci are expected to correlate only weakly with the inbreeding level of an individual. Before using multilocus heterozygosity estimates in studies of inbreeding, their ability to capture information on inbreeding in the given setting should be tested. A convenient method for this is to compute the heterozygosity-heterozygosity correlation, i.e. the mean correlation between multilocus heterozygosity estimates calculated from random samples of loci, which should be positive if multilocus heterozygosity carries a signature of inbreeding. Rhh is an extension package for the statistical software r that estimates this correlation and calculates three measures of individual multilocus heterozygosity: homozygosity by loci, internal relatedness and standardized heterozygosity. The extension package is available through the CRAN (http://cran.r-project.org) and has a homepage at http://www.helsinki.fi/biosci/egru/research/software.

Sex reversal has been suggested to have profound implications for the evolution of sex chromosomes and population dynamics in ectotherms. Occasional sex reversal of genetic males has been hypothesized to prevent the evolutionary decay of nonrecombining Y chromosomes caused by the accumulation of deleterious mutations. At the same time, sex reversals can have a negative effect on population growth rate. Here, we studied phenotypic and genotypic sex in the common frog (Rana temporaria) in a subarctic environment, where strongly female-biased sex ratios have raised the possibility of frequent sex reversals. We developed two novel sex-linked microsatellite markers for the species and used them with a third, existing marker and a Bayesian modelling approach to study the occurrence of sex reversal and to determine primary sex ratios in egg clutches. Our results show that a significant proportion (0.09, 95% credible interval: 0.04-0.18) of adults that were genetically female expressed the male phenotype, but there was no evidence of sex reversal of genetic males that is required for counteracting the degeneration of Y chromosome. The primary sex ratios were mostly equal, but three clutches consisted only of genetic females and three others had a significant female bias. Reproduction of the sex-reversed genetic females appears to create all-female clutches potentially skewing the population level adult sex-ratio consistent with field observations. However, based on a simulation model, such a bias is expected to be small and transient and thus does not fully explain the observed female-bias in the field.