For evolution to occur over time, it is necessary for animals and plants to show phenotypic variation. If the individuals within populations of a species do not show observable differences among themselves, there will be a lack of driving force for natural selection to act on and decide which characteristic gets inherited from one generation to the next. It is hence important to study phenotypic variation, especially against environmental gradients such as latitude and altitude, which gives us an insight into the pattern of change according to essential factors such as temperature and length of seasons. The latter would impose time constraints on growing populations, leading to periods of unfavourable conditions limiting their growth and development. In many cases, such organisms would tend to compensate for the period of slow growth and catch up to the others that did not have to endure the same situation and grow to the same size as them. This study aims to find differences in three key larval life-history traits of the moor frog (Rana arvalis), namely metamorphic mass, larval period, and growth rate, and find what kind of pattern is observed in case of these phenotypic variations. It also aims to find differences in the strength of compensatory response between populations from lower and higher latitudes. A common garden experiment was conducted with populations originating from both sides of the Baltic Sea, ranging from southern Sweden and Latvia to central Finland and northern Sweden. It was expected that the northern populations would grow faster and show a countergradient variation pattern since they are faced with more strict time constraints at higher latitudes, but in most cases, we observed a co-gradient pattern, wherein the environmental effect amplifies the individual’s genetic predisposition instead of opposing it. We also observed a stronger compensatory response in the northern populations as compared to their southern counterparts. Effects of climate change and subsequent rise in temperatures making the environment unpredictable over time could be used to speculate about the reason behind the results obtained. Epigenetics could also be used as an approach to study long lasting changes in an organism’s gene expression to make it adapt better to changing conditions and hence show different patterns of variation from studies in the past. Studying such changes, expected or not, is important to keep up with the needs of the species that require conservation, and will help conservation biologists to formulate strategies that would be effective even in the face of constant change in the world.

<p>Dispersal is an important factor in animal ecology. Anurans (frogs and toads) are often philopatric (home loving) but some specimens in a population usually have the capacity to disperse relatively long distances. In this study I investigated the colonization of newly constructed ponds in the southwest of Sweden by three anuran species: The common toad (Bufo bufo), the moor frog (Rana arvalis) and the common frog (Rana temporaria). The ponds were constructed between two and five years ago and were now as frequently occupied as older source ponds in the area. For the common toad and the common frog there was no correlation between distance to source populations and degree of colonization. The moor frog was more common in ponds that were situated in the vicinity of older source ponds with ample populations. The main impression was that these species rapidly colonize newly constructed ponds, at least within moderate distances from source populations. There were some differences between the species though and it seems like the moor frog have more limited dispersal abilities than the other two species.</p>

Dispersal is an important factor in animal ecology. Anurans (frogs and toads) are often philopatric (home loving) but some specimens in a population usually have the capacity to disperse relatively long distances. In this study I investigated the colonization of newly constructed ponds in the southwest of Sweden by three anuran species: The common toad (Bufo bufo), the moor frog (Rana arvalis) and the common frog (Rana temporaria). The ponds were constructed between two and five years ago and were now as frequently occupied as older source ponds in the area. For the common toad and the common frog there was no correlation between distance to source populations and degree of colonization. The moor frog was more common in ponds that were situated in the vicinity of older source ponds with ample populations. The main impression was that these species rapidly colonize newly constructed ponds, at least within moderate distances from source populations. There were some differences between the species though and it seems like the moor frog have more limited dispersal abilities than the other two species.

Growth rate is an important life history trait, which impacts fitness indirectly through its effect on the age and size at maturity, as well as directly through costs associated with accelerated growth such as increased predation risk. Genetic variation and plasticity in growth are widespread in nature, and local adaptation of growth rate may evolve due to divergent selection in different environments, for example related to predation risk, temperature or time constraints. I studied local adaptation of larval life history in the moor frog Rana arvalis, in a local network of ponds close to Uppsala. Local adaptation of growth rate and survival was studied in a reciprocal transplant experiment between ponds with different habitat characteristics. Meanwhile, differences among the populations in intrinsic growth, activity and response to predation were studied in a common garden experiment in the laboratory, where tadpoles were raised in the presence or absence of a predator and tested in direct predation trials. In the field, differences in growth among populations were found, independent of which pond the tadpoles were raised in, indicating that the ponds were similar growth environments. Survival differences among the populations depended on the pond, but local populations did not do better than foreign ones. In the laboratory, similar patterns in growth rate were found. All populations were highly plastic in their response to predation, having lower growth and activity in the predator-induced treatment and decreased mortality in the predation trials. Tadpole size was an important factor in escaping predation. One population clearly grew faster than the others in the field and in the lab, which could be explained in terms of its habitat of origin but was most likely related to the relatively late hatching of this population. Future studies are necessary concerning the possible costs of this accelerated growth and the importance of breeding phenology. Apart from the one differential population, I did not find evidence of local adaptation in the field or in the laboratory. The influence of habitat characteristics on tadpole life history was difficult to study, due to the limited number of ponds and many environmental differences among them. However, this thesis was a valuable pilot study concerning the design of experiments to study factors promoting and constraining local adaptation in landscape mosaics. An understanding of local adaptation at the scale at which gene flow occurs is important for the conservation of populations in fragmented landscapes as well as for the study of ecological speciation.