The marine otter Lontra felina lives along the Pacific coast of South America from 6°S to 56°S. A method for estimating marine otter abundance is described and a comparison of the characteristics of the terrestrial habitat of this species in southern Chile is made. From June 1999 to June 2000, we conducted eight hours of observations on one day each month at four study sites. An average of 3.8 observable otters/km were recorded, with significant differences between sites but no systematic trends with regard to season. Observable pups were recorded year-round. Otters spent 80% of their time out of view, engaged in behaviours other than feeding; observable otters were mostly seen feeding. The methodology described is effective for indexing abundances at small geographic scales. The marine otter needs both an aquatic habitat for foraging and a terrestrial habitat with an abundance of safe shelters, which, in turn, could limit the distribution of the species when human settlers and domestic dogs utilise the terrestrial habitats.

When dispersal is not an option to evade warming temperatures, compensation through behavior, plasticity, or evolutionary adaptation is essential to prevent extinction. In this work, we evaluated whether there is physiological plasticity in the thermal performance curve (TPC) of maximum jumping speed in individuals acclimated to current and projected temperatures and whether there is an opportunity for behavioral thermoregulation in the desert landscape where inhabits the northernmost population of the endemic frog Pleurodema thaul. Our results indicate that individuals acclimated to 20°C and 25°C increased the breath of their TPCs by shifting their upper limits with respect to when they were acclimated at 10°C. In addition, even when dispersal is not possible for this population, the landscape is heterogeneous enough to offer opportunities for behavioral thermoregulation. In particular, under current climatic conditions, behavioral thermoregulation is not compulsory as available operative temperatures are encompassed within the population TPC limits. However, for severe projected temperatures under climate change, behavioral thermoregulation will be required in the sunny patches. In overall, our results suggest that this population of Pleurodema thaul will be able to endure the worst projected scenario of climate warming as it has not only the physiological capacities but also the environmental opportunities to regulate its body temperature behaviorally.

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Summary1. The distribution of additive vs. non-additive genetic variation in natural populations represents a central topic of research in evolutionary/organismal biology. For evolutionary physiologists, functional or whole-animal performance traits ('physiological traits') are frequently studied assuming they are heritable and variable in populations. 2. Physiological traits of evolutionary relevance are those functional capacities measured at the whole-organism level, with a potential impact on fitness. They can be classified as capacities (or performances) or costs, the former being directly correlated with fitness and the latter being inversely correlated with fitness (usually assumed as constraints). 3. In spite of their obvious adaptive significance, the additive genetic variation in physiological traits, and its relative contribution to phenotypic variance (or narrow-sense heritability) in comparison with maternal, dominance or epistatic variance, is known only for a few groups such as insects and mammals. 4. In this study, we assessed the additive and maternal/non-additive genetic variation in a suite of physiological and morphological traits in populations of the land snail Cornu aspersum. 5. Except for dehydration rate (h 2 = 0Á32 AE 0Á15), egg mass (h 2 = 0Á82 AE 0Á30) and hatchling mass (h 2 = 1Á01 AE 0Á31; population = fixed effect), we found very low additive genetic variation. Large non-additive/maternal effects were found in all traits. Cage effects did not change the results, indicating low contribution of common environmental variance to our results. No differences were found between the phenotypic and non-additive genetic variance/covariance matrices. 6. Even though we compared populations across 1300 km in a common garden set-up, our results suggest an absence of physiological as well as morphological differentiation in these populations. 7. These results contrast with previous analyses in the original distributional range of this species, which found high additive genetic variation in morphological traits. These are intriguing results demanding further quantitative genetic studies in the original distributional range of this species as well as the history of colonization of this invasive species.

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Abstract. Standard metabolic rate (SMR) and resistance to body dehydration (BD) are important physiological traits that have an effect on water balance and the amount of energy available for activity and production, and thus could contribute to variation in life history traits expressed across a range of environments. Few studies have tested whether SMR and BD show consistent between-individual variation in molluscs. Significant repeatability of SMR and BD indicates that the traits might be heritable and therefore a possible target for natural selection, so describing the repeatability of SMR and BD is important in studies of phenotypic variability. Here, we studied energy metabolism (body mass-corrected SMR) and the change in the scaling relationship of SMR and body mass in response to time between measurements in the giant garden slug Limax maximus. Limax maximus is one of the most invasive terrestrial molluscs, with a wide geographical distribution, and is considered an important pest of horticultural and agricultural crops. Our results show that L. maximus follows the expected relationship of increasing SMR with increasing mass, but the scaling exponent varies through time and is different from that described for other gastropods. We also found significant inter-individual variation in VCO 2 Mean , VCO 2 Min , VCO 2 Max , and BD (τ=0.25, 0.29, 0.24, 0.22, p<0.05, respectively), and significant repeatability of body mass (τ=0.90). To our knowledge, this is the first comprehensive analysis of the repeatability of body mass-corrected SMR and BD in terrestrial slugs. Our results suggest that energy metabolism and water balance could potentially respond to selection.

Life-history evolution-the way organisms allocate time and energy to reproduction, survival, and growth-is a central question in evolutionary biology. One of its main tenets, the allocation principle, predicts that selection will reduce energy costs of maintenance in order to divert energy to survival and reproduction. The empirical support for this principle is the existence of a negative relationship between fitness and metabolic rate, which has been observed in some ectotherms. In juvenile animals, a key function affecting fitness is growth rate, since fast growers will reproduce sooner and maximize survival. In principle, design constraints dictate that growth rate cannot be reduced without affecting maintenance costs. Hence, it is predicted that juveniles will show a positive relationship between fitness (growth rate) and metabolic rate, contrarily to what has been observed in adults. Here we explored this problem using land snails (Cornu aspersum). We estimated the additive genetic variance-covariance matrix for growth and standard metabolic rate (SMR; rate of CO2 production) using 34 half-sibling families. We measured eggs, hatchlings, and juveniles in 208 offspring that were isolated right after egg laying (i.e., minimizing maternal and common environmental variance). Surprisingly, our results showed that additive genetic effects (narrow-sense heritabilities, h(2)) and additive genetic correlations (rG) were small and nonsignificant. However, the nonadditive proportion of phenotypic variances and correlations (rC) were unexpectedly large and significant. In fact, nonadditive genetic effects were positive for growth rate and SMR ([Formula: see text]; [Formula: see text]), supporting the idea that fitness (growth rate) cannot be maximized without incurring maintenance costs. Large nonadditive genetic variances could result as a consequence of selection eroding the additive genetic component, which suggests that past selection could have produced nonadditive genetic correlation. It is predicted that this correlation is reduced when adulthood is attained and selection starts to promote the reduction in metabolic rate.