Search

Theoretical models indicate that the evolution of biparental care depends on how parents behaviorally negotiate their level of care in response to those of their partner and whether sexes and individuals consistently vary in their response (compensatory response). While compensatory response has been widely investigated empirically, its repeatability has rarely been assessed. In this study, we used a reaction norm approach to investigate the repeatability of the compensatory offspring provisioning of a parent after temporary removal of its partner in the pied flycatcher (Ficedula hypoleuca) across different breeding seasons and partners. We found that only females partially compensated for the short-term removal of the partner and their response was significantly repeatable across years while breeding with different partners. This study highlights the importance of considering among individual differences in negotiation rules to better understand the role of negotiation mechanisms in the evolution of parental care strategies.

Theoretical models indicate that the evolution of biparental care depends on how parents behaviourally negotiate their level of care in response to those of their partner and whether sexes and individuals consistently vary in their response (compensatory response). While the compensatory response has been widely investigated empirically, its repeatability has rarely been assessed. In this study, we used a reaction norm approach to investigate the repeatability of the compensatory offspring provisioning of a parent after temporary removal of its partner in the pied flycatcher (Ficedula hypoleuca) across different breeding seasons and partners. We found that only females partially compensated for the short-term removal of the partner and their response was significantly repeatable across years while breeding with different partners. This study highlights the importance of considering among individual differences in negotiation rules to better understand the role of negotiation mechanisms in the evolution of parental care strategies.

Theoretical models indicate that the evolution of biparental care depends onhow parents behaviourally negotiate their level of care in response to thoseof their partner and whether sexes and individuals consistently vary in theirresponse (compensatory response). While the compensatory response hasbeen widely investigated empirically, its repeatability has rarely beenassessed. In this study, we used a reaction norm approach to investigatethe repeatability of the compensatory offspring provisioning of a parentafter temporary removal of its partner in the pied flycatcher (Ficedula hypo-leuca) across different breeding seasons and partners. We found that onlyfemales partially compensated for the short-term removal of the partnerand their response was significantly repeatable across years while breedingwith different partners. This study highlights the importance of consideringamong individual differences in negotiation rules to better understand therole of negotiation mechanisms in the evolution of parental care strategies.

Extra-pair paternity (EPP) has been broadly reported in socially monogamous bird species and it has been hypothesized that females engage in extra-pair copulations to increase the genetic variability of the offspring and to reduce the risk of inbreeding and genetic incompatibilities. This hypothesis makes two predictions: within populations, females should engage with more dissimilar/heterozygous males and, among popula - tions, females should pursue more frequently EPP in populations characterized by a lower genetic variability and a higher homozygosity. However, support is still unclear throughout literature, and usually involves the study of a single population. We compared a peripheral population of rock sparrow Petronia petronia living at the marginal distribution of the species and characterized by a high EPP level (> 50%) (Italian Alps) with a population located in the centre of the species’ distribution (central Spain), to understand if variations in EPP could be linked to differences in mean heterozygosity and genetic similarity both between and within populations. EPP in the Spanish population was 18.1%, three times lower than that observed in the Alpine one (51.2%), and this difference remained fairly constant across different years. Supporting the between populations prediction, we found lower heterozygosity and reduced allelic richness in the Alpine population compared to the Spanish one. In contrast, social and extra-pair males, as well as within and extra-pair offspring, did not significantly differ in terms of genetic similarity and heterozygosity within brood in either population. Social and extra-pair males did not differ in tarsus size, body weight or yellow badge size, suggesting that females were not choosing extra-pair partners based on heterozygosity, genetic similarity or phenotypic quality. Although based on a limited sample in the within population analysis, our results indicate that EPP may evolve in response to a low level of genetic vari

Dataset of the scientific article "Heterozygosity, genetic similarity and extra-pair paternity variation in two populations of Rock Sparrow Petronia petronia: a within- and between- populations comparison".