Development of microsatellite loci in the European Dipper, Cinclus cinclus

Eighteen polymorphic microsatellite DNA loci were isolated in the Central European subspecies of the European Dipper (Cinclus cinclus aquaticus). The loci were tested for polymorphism using a test panel of 24 breeding birds. Numbers of alleles ranged from 2 to 21 per locus and expected heterozygosities varied between 0.47 and 0.83. Two loci (Cici10 and Cici12) proved to be Z-linked. Some pairs of loci exhibited significant linkage disequilibrium but not the two loci that are located on the Z-chromosome. This pattern suggests that demographic effects rather than physical linkage are likely responsible for the observed levels of linkage disequilibrium. These loci will be useful for applied conservation projects and for investigations of the dispersal and mating patterns of European and other dipper

Development of microsatellite loci in the European Dipper, Cinclus cinclus

Eighteen polymorphic microsatellite DNA loci were isolated in the Central European subspecies of the European Dipper (Cinclus cinclus aquaticus). The loci were tested for polymorphism using a test panel of 24 breeding birds. Numbers of alleles ranged from 2 to 21 per locus and expected heterozygosities varied between 0.47 and 0.83. Two loci (Cici10 and Cici12) proved to be Z-linked. Some pairs of loci exhibited significant linkage disequilibrium but not the two loci that are located on the Z-chromosome. This pattern suggests that demographic effects rather than physical linkage are likely responsible for the observed levels of linkage disequilibrium. These loci will be useful for applied conservation projects and for investigations of the dispersal and mating patterns of European and other dippers

Spacing behavior of the middle spotted woodpecker in central Europe.

Knowledge of the ranging behavior and spatial requirements of a species is fundamental for establishing meaningful conservation strategies. Such information is lacking for the middle spotted woodpecker (Dendrocopos medius), a species endangered throughout its westpalearctic range. By radiotracking, we studied spacing behavior of this habitat specialist in a lowland oak forest of northeastern Switzerland from 1992-1996. Home range and core area size decreased from winter to late spring, with males and females having home ranges of similar size. Overlap of male home ranges was highest in winter (up to 40%) and lowest in late spring, whereas core area overlap remained low. For both home ranges and core areas, overlapping parts were used randomly in winter but more often than expected in early spring. Overlap of female ranges and of core areas did not change from early to late spring, and the shared parts of these home ranges were used as expected in both seasons. Aggressive interactions were most common in March and April and occurred mainly between individuals of the same sex. Our results suggest that the middle spotted woodpecker is not territorial in winter but defends nearly exclusive territories during spring, with both sexes participating to similar degrees in territorial defense. Based on this seasonal territoriality, we propose consideration of core areas in early spring (Mar and Apr) as a reliable estimate of the area requirements of the species to be used in management plans

Becker-et-al_JEB_pedigree

Pedigree Data White-throated dipper (Cinclus cinclus), Pruned Pedigree, Long-term Study Zurich, Switzerland

Data from: Phenotype-associated inbreeding biases estimates of inbreeding depression in a wild bird population

Inbreeding depression is usually quantified by regressing individual phenotypic values on inbreeding coefficients, implicitly assuming there is no correlation between an individual's phenotype and the kinship coefficient to its mate. If such an association between parental phenotype and parental kinship exists, and if the trait of interest is heritable, estimates of inbreeding depression can be biased. Here we first derive the expected bias as a function of the covariance between mean parental breeding value and parental kinship. Subsequently, we use simulated data to confirm the existence of this bias, and show that it can be accounted for in a quantitative genetic animal model. Finally, we use long-term individual-based data for white-throated dippers (Cinclus cinclus), a bird species in which inbreeding is relatively common, to obtain empirical estimate of this bias. We show that during part of the study period, parents of inbred birds had shorter wings than those of outbred birds, and as wing length is heritable, inbred individuals were smaller, independent of any inbreeding effects. This resulted in the overestimation of inbreeding effects. Similarly, during a period when parents of inbred birds had longer wings, we found that inbreeding effects were underestimated. We discuss how such associations may have arisen in this system, and why they are likely to occur in others, too. Overall, we demonstrate how less biased estimates of inbreeding depression can be obtained within a quantitative genetic framework, and suggest that inbreeding and additive genetic effects should be accounted for simultaneously whenever possible

Becker-et-al_JEB_wing-data

Morphological Data, White-throated dipper (Cinclus cinclus), Long-term Study Zurich, Switzerland. See file for more information

Phenotype-associated inbreeding biases estimates of inbreeding depression in a wild bird population

Inbreeding depression is usually quantified by regressing individual phenotypic values on inbreeding coefficients, implicitly assuming there is no correlation between an individual's phenotype and the kinship coefficient to its mate. If such an association between parental phenotype and parental kinship exists, and if the trait of interest is heritable, estimates of inbreeding depression can be biased. Here we first derive the expected bias as a function of the covariance between mean parental breeding value and parental kinship. Subsequently, we use simulated data to confirm the existence of this bias, and show that it can be accounted for in a quantitative genetic animal model. Finally, we use long-term individual-based data for white-throated dippers (Cinclus cinclus), a bird species in which inbreeding is relatively common, to obtain an empirical estimate of this bias. We show that during part of the study period, parents of inbred birds had shorter wings than those of outbred birds, and as wing length is heritable, inbred individuals were smaller, independent of any inbreeding effects. This resulted in the overestimation of inbreeding effects. Similarly, during a period when parents of inbred birds had longer wings, we found that inbreeding effects were underestimated. We discuss how such associations may have arisen in this system, and why they are likely to occur in others, too. Overall, we demonstrate how less biased estimates of inbreeding depression can be obtained within a quantitative genetic framework, and suggest that inbreeding and additive genetic effects should be accounted for simultaneously whenever possible