Capture and long‐distance translocation of cleaner fish to control lice infestations on marine salmonid farms has the potential to influence wild populations via overexploitation in source regions, and introgression in recipient regions. Knowledge of population genetic structure is therefore required. We studied the genetic structure of ballan wrasse, a phenotypically diverse and extensively used cleaner fish, from 18 locations in Norway and Sweden, and from Galicia, Spain, using 82 SNP markers. We detected two very distinct genetic groups in Scandinavia, northwestern and southeastern. These groups were split by a stretch of sandy beaches in southwest Norway, representing a habitat discontinuity for this rocky shore associated benthic egg‐laying species. Wrasse from Galicia were highly differentiated from all Scandinavian locations, but more similar to northwestern than southeastern locations. Distinct genetic differences were observed between sympatric spotty and plain phenotypes in Galicia, but not in Scandinavia. The mechanisms underlying the geographic patterns between phenotypes are discussed, but not identified. We conclude that extensive aquaculture‐mediated translocation of ballan wrasse from Sweden and southern Norway to western and middle Norway has the potential to mix genetically distinct populations. These results question the sustainability of the current cleaner fish practice.
The cold-adapted polar cod Boreogadus saida, a key species in Arctic ecosystems, is vulnerable to global warming and ice retreat. In this study, 1257 individuals sampled in 17 locations within the latitudinal range of 75–81°N from Svalbard to East Siberian Sea were genotyped with a dedicated suite of 116 single-nucleotide polymorphic loci (SNP). The overall pattern of isolation by distance (IBD) found was driven by the two easternmost samples (East Siberian Sea and Laptev Sea), whereas no differentiation was registered in the area between the Kara Sea and Svalbard. Eleven SNP under strong linkage disequilibrium, nine of which could be annotated to chromosome 2 in Atlantic cod, defined two genetic groups of distinct size, with the major cluster containing seven-fold larger number of individuals than the minor. No underlying geographic basis was evident, as both clusters were detected throughout all sampling sites in relatively similar proportions (i.e. individuals in the minor cluster ranging between 4 and 19% on the location basis). Similarly, females and males were also evenly distributed between clusters and age groups. A differentiation was, however, found regarding size at age: individuals belonging to the major cluster were significantly longer in the second year. This study contributes to increasing the population genetic knowledge of this species and suggests that an appropriate management should be ensured to safeguard its diversity.
Atlantic herring (Clupea harengus) has a complex population structure and displays a variety of reproductive strategies. Differences in reproductive strategies among herring populations are linked to their time of spawning, as well as to their reproductive investment which can be an indicator for migratory vs. stationary behavior. These differences are reflected in the number of oocytes (fecundity) and the size of the oocytes prior spawning. We studied potential mixing of herring with different reproductive strategies during the spring spawning season on a coastal spawning ground. It has been hypothesized that both spring and autumn spawning herring co-occur on this specific spawning ground. Therefore, we investigated the reproductive traits oocyte size, fecundity, fertilization success as well as length of the hatching larvae during the spring spawning season from February to April. We used a set of 11 single nucleotide polymorphism markers (SNPs), which are associated with spawning season, to genetically identify autumn and spring spawning herring. Reproductive traits were investigated separately within these genetically distinct spawning types. Furthermore, we used multivariate analyses to identify groups with potentially different reproductive strategies within the genetic spring spawners. Our results indicate that mixing between ripe spring and autumn spawners occurs on the spawning ground during spring, with ripe autumn spawners being generally smaller but having larger oocytes than spring spawners. Within spring spawners, we found large variability in reproductive traits. A following multivariate cluster analysis indicated two groups with different reproductive investment. Comparisons with other herring populations along the Norwegian coastline suggest that the high variability can be explained by the co-occurrence of groups with different reproductive investments potentially resulting from stationary or migratory behavior. Fertilization success and the length of the hatching larvae decreased with progression of the spawning season, with strong inter-individual variation, supporting our findings. Incorporating such complex population dynamics into management strategies of this species will be essential to build its future population resilience.
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