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6 results for “Pelodytes punctatus”
FIG. 4 in Age structure and growth in an isolated population of Pelodytes punctatus in northern Spain
FIG. 4. Growth in length body (SVL) of P. punctatus in Burgos, Spain. Mean and range are given at each age. Curves fitted to the Von Bertalanffy equation.
FIG. 1 in Age structure and growth in an isolated population of Pelodytes punctatus in northern Spain
FIG. 1. Cross-sections at the diaphysis of phalanges for P. punctatus in Burgos, Spain. (A) Male, 40.3 mm SVL, six LAGs; (B) female, 45.5 mm SVL, five LAGs. Arrows, LAGs; ml, metamorphosis line; eb, endosteal bone.
FIG. 3 in Age structure and growth in an isolated population of Pelodytes punctatus in northern Spain
FIG. 3. Snout–vent length distribution of P. punctatus in Burgos, Spain. Black bars, males; grey bars, females.
Data from: Phenotypic plasticity allows the Mediterranean parsley frog Pelodytes punctatus to exploit two contrasted temporal niches under continuous gene flow
Environmental changes, such as climate change, lead to the opening of new niches. In such situations, species that adapt to new niches can survive and/or expand their ranges. However, gene flow can hamper genetic adaptation to new environments. Alternatively, recent models have highlighted the importance of phenotypic plasticity in tracking environmental change. In this study, we illustrate how plasticity allows an amphibian species to exploit two very different climatic niches under continuous gene flow. In the Mediterranean region, the parsley frog Pelodytes punctatus breeds both in spring, as do most other species, and in autumn, a temporal niche not exploited by most other species, but which may become increasingly important with global warming. Conditions of development are dramatically different between the two seasons and deeply impact tadpole life-history traits. To determine whether these temporal niches are exploited by two genetically differentiated sub-populations, or whether the bimodal phenology arises in a panmictic population displaying plastic life-history traits, we use two complementary approaches. We measure both molecular genetic differentiation and quantitative-trait differentiation between spring and autumn cohorts, using microsatellites an common garden experiments respectively. Seasonal cohorts were not genetically differentiated and differences in tadpole life-history between cohorts were not maintained in laboratory conditions. We conclude that phenotypic plasticity, rather than genetic adaptation, allows Parsley frog to exploit two contrasted temporal niches.
Data from: Phenotypic plasticity allows the Mediterranean parsley frog Pelodytes punctatus to exploit two contrasted temporal niches under continuous gene flow
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FIG. 2 in Age structure and growth in an isolated population of Pelodytes punctatus in northern Spain
FIG. 2. Age distribution of P. punctatus in Burgos, Spain. Black bars, males; grey bars, females.
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