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SummaryDuring their flightless summer moult, Taiga Bean GeeseAnser fabalis fabalisgather at communal moulting sites. Individuals from the Nord-Trøndelag breeding area in Norway have been observed to join with local individuals on moulting sites in Vilhelmina Municipality, Sweden. These two groups show distinct features in breeding habitat and migratory behaviour, but are they also genetically distinct? We used 12 microsatellite loci for genotyping 109 blood, feather and faecal samples from three sampling areas (Røyrvik in Norway and Stalon and Nästansjö in Sweden) to examine genetic diversity and structure. Clustering and Principal Coordinate analyses of all samples unveiled at least two distinct clusters, which were unevenly distributed over the sampling sites. Grouped by sampling sites, AMOVA and FSTanalyses showed that samples from the three sites differed genetically. These differences were larger between Røyrvik and Nästansjö than between Stalon and the other two. Relatedness was high among the Røyrvik samples. From our results we conclude that one of the clusters describes the Røyrvik breeding subpopulation, while the other(s) breed mainly in Sweden. Although these subpopulations simultaneously use the same moulting area in Vilhelmina, they appear to be ecologically, behaviourally and genetically distinct, in particular the Røyrvik sub-population. For goose conservation and management, we suggest that the Nord-Trøndelag (Røyrvik) subpopulation is considered a separate flyway management unit. Unravelling the Swedish sub-populations will need further study. For bird conservation is general, we suggest active genetic sampling for detailed population structure analyses and subsequent differentiated conservation and/or management schemes.

Basic knowledge about the genetic mating system is lacking for the great majority of the approximately 10,000 extant bird species. Filling this knowledge gap is not only critical for a comprehensive understanding of the reproductive ecology of each particular species, but also for increasing the power of comparative approaches to uncover and explain interspecific patterns of variation in avian reproductive traits. Using six polymorphic microsatellite markers, we here present the first parentage study in the socially monogamous Fieldfare Turdus pilaris. In parallel, we also examined variation in sperm morphology and relationships between sperm traits and paternity loss of social males. Across two study years, extra-pair paternity was detected in 46.4% (95% CI: 28.9%−64.9%) of 28 broods, and on average 27.6% (95% CI: 16.8%−41.9%) of nestlings per brood were extra-pair offspring in a population in central Norway. The observed extra-pair paternity rates fall within the range of reported estimates of extra-pair paternity for four congeneric Turdus species (between 36% and 65% of broods and 27% and 46% of nestlings). Sperm total length was 87.0 ± 2.9 (SD) μm (range 79.7-96.8 μm) and 59.3% (95% CI: 37.1%−73.3%) of the total phenotypic variation in sperm total length was explained by differences between sperm samples collected from 17 different males. The among-sample coefficient of variation in mean sperm total length was 2.70% (95% CI: 1.99%−3.17%). We found no evidence for effects of sperm total length or relative midpiece length on loss of paternity among broods of 13 males.

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During the 1950s and 1970s the osprey (Pandion haliaetus) experienced a dramatic population crash and remains of conservation concern in several parts of the world. We isolated 37 microsatellite loci and assessed these in ospreys sampled in the UK and Norway (using mouth swabs/feathers). From 26 loci variable in four ospreys, we selected 13, combined these into two multiplex-PCR sets and included a sex-typing marker. Additional markers confirmed sexes. In 17 ospreys, feather-sampled in central Norway, we found 3–10 alleles per locus. The 13 loci are autosomal (heterozygotes were present in both sexes) and observed heterozygosities ranged from 0.24 to 0.94. The combined probability of identity for the 13 loci was 8.0 × 10−12. These microsatellite loci will be useful for genetic monitoring, parentage analysis and population genetic studies of the osprey.Electronic supplementary materialThe online version of this article (doi:10.1007/s12686-015-0497-4) contains supplementary material, which is available to authorized users.