We investigated the effect of water constraints on yearling Lacerta vivipara, a widespread species of lizard inhabiting European peat bogs and heath land. We conducted a laboratory experiment to investigate plasticity of growth rate, activity level and preferred body temperature. We subjected individuals of two source habitats (dry vs humid) to two laboratory conditions of water supply resulting in different air relative humidity and water availability (high vs low). We observed that a low water supply induced a lower growth rate and lower activity level, suggesting that growth limitation is correlated with adaptive responses to avoid dehydration. However, individuals from the two habitats selected different body temperatures when restricted in water and showed different ratios between growth and activity. This suggests that there is population variability in phenotypic plasticity with respect to water availability in the habitat. Field observations conducted in six natural populations, classified into two groups (dry vs humid habitat) also suggest that growth rate in nature is constrained by water availability.

Summary 1.Although little investigated, developmental processes that generate dispersal condition evolution of this behaviour. We have shown previously prenatal and postnatal influences on dispersal in the common lizard ( Lacerta vivipara ). The observation of these developmental processes was based on independent experiments; our primary goal in this paper is to test their interactions. Interactions could indeed be a source of inconsistencies in studies because they can mask, or even reverse, effects of factors treated additively. 2. We studied dispersal of juveniles released in natura from 416 pregnant females captured in the field. We used a factorial design to test interactions among the maternal habitat (dry vs. humid), prenatal conditions (temperature, humidity), and postnatal environments (dry vs. humid). 3. We found that juvenile dispersal was dependent on the humidity level at different developmental stages, but with varying and sometimes opposite effects. Dispersal was also influenced by the temperature during gestation and by populational differences not related to humidity (differences between replicated populations for the maternal and postnatal habitats). 4. These results confirm our previous findings that dispersal of the common lizard is condition-dependent and has multiple causation. In addition, most of the effects exhibited interactions, and the ontogeny of dispersal appeared as a sequential process where the maternal habitat conditioned prenatal influences, and the prenatal environment modulated postnatal influences. 5. The robustness of our results is supported by the finding of the same interactions in independent tests on both juvenile males and females. This militates in favour of future studies on the multiple causation of dispersal because the same dispersal status might originate from different causes, and different dispersal outcomes might be due to the same factor.

Parasites affect the life‐histories and fitness of their hosts. It has been demonstrated that the ability of the immune system to cope with parasites partly depends on environmental conditions. In particular, stressful conditions have an immunosuppressive effect and may affect disease resistance. The relationship between environmental stress and parasitism was investigated using a blood parasite of the common lizard Lacerta vivipara. In laboratory cages, density and additional stressors had a significant effect on the intensity of both natural parasitaemia and parasitaemia induced by experimental infection. Four weeks after infection, crowded lizards had three times more parasites than noncrowded lizards. After 1 month of stress treatment, naturally infected lizards had a significantly higher level of plasma corticosterone and a higher parasite load than nonstressed individuals. In seminatural enclosures, stress induced by the habitat quality affected both the natural blood parasite prevalence and the intensity of parasitaemia of the host.

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Correlation between intraspecific phenotypic variability and variation of environmental conditions could reflect adaptation. Different phenotypes may result from differential expression of a genotype in different environments (phenotypic plasticity) or from expression of different genotypes (genetic diversity). Populations of Lacerta vivipara exhibit larger adult body length, lower age at maturity, higher fecundity, and smaller neonatal size in humid habitats compared to dry habitats. We conducted reciprocal transplants of juvenile L. vivipara to test for the genetic or plastic origin of this variation. We captured gravid females from four populations that differed in the relative humidity of their habitats, and during the last 2 to 4 weeks of gestation, we manipulated heat and water availability under laboratory conditions. Juveniles were released into the different populations and families were divided to compare growth rate and survival of half-sibs in two environments. Growth rate and survival were assessed using capture-recapture techniques. Growth rate was plastic in response to postnatal conditions and did not differ between populations of origin. Survival differed between populations of origin, partially because of differences in neonatal body length. The response of juvenile body length and body condition to selection in the different habitats was affected by the population of origin. This result cannot be simply interpreted in terms of adaptation; however, phenotypic plasticity of fecundity or juvenile size most probably resulted in adaptive reproductive strategies. Adaptation to the habitat by means of genetic specialization was not detected. Further investigation is needed to discriminate between genetic and long-term maternal effects.