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Highly migratory species pose unique conservation and management challenges, especially when significant mortality occurs away from breeding concentrations. Population genetics and genomics may help with the appropriate management of these species by (1) determining the population genetic structure of a species across its range, and (2) allowing the assignment of individuals to their breeding source. The northern fulmar (Fulmarus glacialis; Procellariiformes: Procellariidae) is a seabird species that breeds in colonies throughout the North Atlantic and Pacific oceans. This species ranges widely across ocean basins during the non-breeding season and is exposed to a variety of threats throughout the annual cycle. The impact of mortality during the nonbreeding season on individual breeding colonies is unknown but has important ramifications for conservation and management. In this study we used restriction site-associated DNA sequencing (RADseq) to provide 6614 genome-wide single nucleotide polymorphisms (SNPs) to investigate population genetic structure of northern fulmars using 127 individuals from six breeding colonies spanning the Atlantic. Additionally, birds of unknown breeding origin were sampled from two locations: (1) offshore in the Labrador Sea, and (2) the Baffin Bay-Davis Strait region (NAFO subarea 0), as bycatch in gillnets set for Greenland halibut (Reinhardtius hippoglossoides). We found weak genetic differentiation among breeding colonies, which we suggest reflects historical associations as well as contemporary gene flow among populations. Most bycatch birds were likely from nearby breeding colonies in the eastern Canadian Arctic, but the exact breeding origins were difficult to determine due to the lack of differentiation between colonies.

DNA extracted from fecal samples contains DNA from the focal species, food, bacteria and pathogens. Most DNA quantification methods measure total DNA and cannot differentiate among sources. Despite the desirability of noninvasive fecal sampling for studying wildlife populations, low amounts of focal species DNA make it difficult to use for next-generation sequencing (NGS), where accurate DNA quantification is critical for normalization. Two factors are required prior to using fecal samples in NGS libraries: (1) an accurate quantification method for the amount of target DNA and (2) a determination of the relative amount of target DNA needed for successful single nucleotide polymorphism genotyping assays. Here, we address these needs by developing primers to amplify a 101 bp region of the nuclear F2 gene and a quantitative PCR (qPCR) assay that allows the accurate quantification of the amount of polar bear (Ursus maritimus) DNA in fecal extracts. We test the assay on pure polar bear DNA extracted from muscle tissue and find a high correlation between fluorometric and qPCR quantifications. The qPCR assay was also successfully used to quantify the amount of DNA derived from polar bears in fecal extractions. Orthologs of the F2 gene have been identified across vertebrates; thus, similar qPCR assays could be developed for other species to enable noninvasive studies.

Ten microsatellite loci were isolated and characterized from Blue-footed (Sula nebouxii) and Peruvian Boobies (S. variegata). The loci were screened in 24 Blue-footed Boobies and 27 Peruvian Boobies: 8 were polymorphic in Blue-footed Boobies with between 2 and 10 alleles per locus and 9 were polymorphic in Peruvian Boobies with between 2 and 12 alleles per locus. Observed heterozygosity ranged from 0.29 to 0.84. These loci were also tested in Brown Boobies (S. leucogaster) and were variably polymorphic. These new loci are currently being used to assess population genetic structure in Blue-footed and Peruvian Boobies and will also be used to examine hybridization between the species.