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Analysing the geographical distribution of evolutionary linages can reveal the potential locations of past refugia and colonisation routes and thus can improve understanding of current patterns of genetic variation and adaptive potential. We analysed 94 full mitogenome sequences to assess phylogeographic relationships amongst ten Arctic char (Salvelinus alpinus) populations, from western Greenland, eastern Greenland, Iceland and Norway. In addition, we excised D‐loop sequences, which were combined with previously published data in order to provide a circumpolar phylogeographical overview. In western Greenland, a secondary contact zone between Arctic and Atlantic evolutionary lineages was identified, spanning >1000 km, which geographically parallels a similar contact zone in Labrador, Canada. In eastern Greenland, Iceland and Norway, the Atlantic lineage was exclusively observed, whereas the northernmost western Greenland populations belonged to the Arctic lineage. The Arctic and Atlantic lineages were estimated to have diverged ca. 400,000 years BP, corresponding to the onset of the Saale glaciation, whereas the time of the most recent common ancestor (TMRCA) of the Arctic lineage was ca. 15,000 years BP. The Atlantic lineage comprised two subclades, with an estimated TMRCA of 60,000 BP, suggesting a complex history involving cryptic refugia or multiple recolonisations. Codon‐based tests revealed no evidence for positive selection within the 13 coding genes, indicating that there are no mitochondrial genetic adaptations within or between lineages. Higher genetic diversity observed within the contact zone likely correlates with higher standing genetic variation that could contribute to adaptive responses and morphological diversification, which Arctic char is renowned. [ABSTRACT FROM AUTHOR]

We contrast two methods for estimating the trends of bowhead whales ( Balaena mysticetus) in West Greenland: (1) double platform visual aerial survey, corrected for missed sightings and the time the whales are available at the surface; and (2) a genetic capture-recapture approach based on a 14-yr-long biopsy sampling program in Disko Bay. The aerial survey covered 39,000 km2 and resulted in 58 sightings, yielding an abundance estimate of 744 whales ( CV = 0.34, 95% CI: 357-1,461). The genetic method relied on determining sex, mitochondrial haplotypes and genotypes of nine microsatellite markers. Based on samples from a total of 427 individuals, with 11 recaptures from previous years in 2013, this resulted in an estimate of 1,538 whales ( CV = 0.24, 95% CI: 827-2,249). While the aerial survey is considered a snapshot of the local spring aggregation in Disko Bay, the genetic approach estimates the abundance of the source of this aggregation. As the whales in Disko Bay primarily are adult females that do not visit the bay annually, the genetic method would presumably yield higher estimates. The studies indicate that an increase in abundance observed between 1998 and 2006 has leveled off. [ABSTRACT FROM AUTHOR]

We assayed blood/tissue fluid samples from 20 harbour porpoises Phocoena phocoena from western Greenland coastal waters for antibodies against the protozoan parasite Toxoplasma gondii by the direct agglutination test (DAT). Nine individuals (45%) were interpreted to be seropositive at 1:40 dilution and 4 (20%) were seropositive up to 1:160. Samples from these individuals were assayed by an enzyme-linked immunosorbent assay (ELISA), and tissue samples of the DAT-positive animals were tested by a nested polymerase chain reaction (nPCR). Results from both methods were negative, suggesting the absence of infection in the tested animals. After chloroform clean-up, all were negative when re-assayed by DAT. We concluded that infection with T. gondii was absent in all 20 animals, despite the initially positive DAT results, and that the false positives resulted from non-specific adherence to tachyzoites in the DAT assay which could be removed by the chloroform clean-up method. Our results suggest that detecting antibodies against T. gondii using the DAT or the modified agglutination technique, particularly on samples from Arctic marine animals which often are rich in lipids, may lead to false positive results. For such samples, the use of ELISA or PCR on available tissue samples may be advocated as confirmatory tests in order to avoid false positives and overestimating seroprevalence.