Hopp til hovedinnholdet

Publications

NIBIOs employees contribute to several hundred scientific articles and research reports every year. You can browse or search in our collection which contains references and links to these publications as well as other research and dissemination activities. The collection is continously updated with new and historical material.

2024

2023

To document See dataset

Abstract

Studies on host–parasite systems that have experienced distributional shifts, range fragmentation, and population declines in the past can provide information regarding how parasite community richness and genetic diversity will change as a result of anthropogenic environmental changes in the future. Here, we studied how sequential postglacial colonization, shifts in habitat, and reduced host population sizes have influenced species richness and genetic diversity of Corynosoma (Acanthocephala: Polymorphidae) parasites in northern European marine, brackish, and freshwater seal populations. We collected Corynosoma population samples from Arctic, Baltic, Ladoga, and Saimaa ringed seal subspecies and Baltic gray seals, and then applied COI barcoding and triple-enzyme restriction-site associated DNA (3RAD) sequencing to delimit species, clarify their distributions and community structures, and elucidate patterns of intraspecific gene flow and genetic diversity. Our results showed that Corynosoma species diversity reflected host colonization histories and population sizes, with four species being present in the Arctic, three in the Baltic Sea, two in Lake Ladoga, and only one in Lake Saimaa. We found statistically significant population-genetic differentiation within all three Corynosoma species that occur in more than one seal (sub)species. Genetic diversity tended to be high in Corynosoma populations originating from Arctic ringed seals and low in the landlocked populations. Our results indicate that acanthocephalan communities in landlocked seal populations are impoverished with respect to both species and intraspecific genetic diversity. Interestingly, the loss of genetic diversity within Corynosoma species seems to have been less drastic than in their seal hosts, possibly due to their large local effective population sizes resulting from high infection intensities and effective intra-host population mixing. Our study highlights the utility of genomic methods in investigations of community composition and genetic diversity of understudied parasites.

To document

Abstract

Aquaculture of the lumpfish (Cyclopterus lumpus L.) has become a large, lucrative industry owing to the escalating demand for “cleaner fish” to minimise sea lice infestations in Atlantic salmon mariculture farms. We used over 10K genome-wide single nucleotide polymorphisms (SNPs) to investigate the spatial patterns of genomic variation in the lumpfish along the coast of Norway and across the North Atlantic. Moreover, we applied three genome scans for outliers and two genotype–environment association tests to assess the signatures and patterns of local adaptation under extensive gene flow. With our ‘global’ sampling regime, we found two major genetic groups of lumpfish, i.e., the western and eastern Atlantic. Regionally in Norway, we found marginal evidence of population structure, where the population genomic analysis revealed a small portion of individuals with a different genetic ancestry. Nevertheless, we found strong support for local adaption under high gene flow in the Norwegian lumpfish and identified over 380 high-confidence environment-associated loci linked to gene sets with a key role in biological processes associated with environmental pressures and embryonic development. Our results bridge population genetic/genomics studies with seascape genomics studies and will facilitate genome-enabled monitoring of the genetic impacts of escapees and allow for genetic-informed broodstock selection and management in Norway.

To document

Abstract

The aim of this study was to evaluate whether sea lice grazing efficiency, behaviour, size variation and cataract development can be improved through selective breeding of lumpfish. A series of studies was conducted over a four-year period where distinctive lumpfish families were established initially from wild caught mature fish and latterly from established breeding lines. Four subsequent trials (called: Phase I-IV) with ten families of lumpfish (N = 480) with a mean (± SD) weight of 46.4 ± 9.4 g (Phase I), 54.8 ± 9.2 g (Phase II), 42.0 ± 7.4 g (Phase III) and 31.3 ± 2.4 g (Phase IV) were distributed among ten sea cages (5 × 5 × 5 m) during autumn 2018 to spring 2022, each stocked with 400–404 Atlantic salmon with an average initial mean (± SD) of 387 ± 9 g (Phase I), 621 ± 15 g (Phase II), 280 ± 16 g (Phase III) and 480 ± 66 g (Phase IV). All the ten cages were stocked with 48 lumpfish (12% stocking density). In all phases there was a large inter-family variation of lice grazing of lumpfish of both L. salmonis and C. elongatus. When sea lice grazing was scaled in relation to sea lice infestation numbers on the salmon the highest sea lice grazing activity was found in Phase IV and in particular in families sired from farmed parents. There was a general trend for mean start weights and standard deviations to decrease as the phases continued. A significant increase was found in frequency of behaviour associated with feeding on natural food sources and grazing sea lice from salmon during each subsequent phase. The increase in incidence of cataracts from start to end of each trial phase was significantly reduced from Phase I (16%) to Phase IV (2%). Overall, present findings showed that sea lice grazing of both L. salmonis and C. elongatus, size variation, cataract prevalence and behaviour types can be enhanced through selection and targeted breeding programs.

To document

Abstract

The adults of the new species Zachvatkinibates svanhovdi A. Seniczak & S. Seniczak sp. nov. are described and illustrated from Norway, and this is the first finding of Zachvatkinibates Shaldybina, 1973 in Fennoscandia. This species is the most similar to Z. quadrivertex (Halbert, 1920), but differs from it mainly by the shape of notogastral setae, posterior tectum of notogaster and lack of postanal porose area Ap, which in Z. quadrivertex is present. In Z. svanhovdi, the prodorsal seta in is long, translamella is narrow, notogastral setae are short and distally pliable, notogastral porose areas are usually oval and of medium size, but Aa can be larger, especially in males. Dorsal crest on tarsus I is present. The cytochrome oxidase I (COI) barcodes (length: 658 bp) of five specimens of the new species are provided; the maximum variation within the species was 2.41% (p-dist). The morphology and ecology of the new species is compared with other Zachvatkinibates species. The knowledge on family Punctoribatidae in Fennoscandia is updated, and Mycobates carli (Schweizer, 1922) is first reported from Norway.

To document

Abstract

The morphological ontogeny of Nanhermannia sellnicki Forsslund, 1958 is described and illustrated. In all juvenile stages the bothridial seta is minute, and two pairs of exobothridial setae are present (exa reduced to its alveolus, exp short). In the larva, the seta f1 is setiform but in the nymphs it is unobservable among cuticular tubercles. Most prodorsal and gastronotal setae of the larva are short while thouse of nymphs are long; seta in and all gastronotal and adanal setae are inserted in small individual depressions. In all instars the leg segments are oval in cross section and relatively thick, and most setae on tarsi are relatively short, thick or conical. The seta d accompanies solenidion σ on all genua, φ1 on tibia I and φ on other tibiae.

To document

Abstract

The morphological ontogeny of Zachvatkinibates svanhovdi A. Seniczak & S. Seniczak, 2023 is described and illustrated. The juveniles of this species are light brown with slightly darker colour on the prodorsum, gastronotal shield, surrounding of gla opening, and legs. The larva has 12 pairs of gastronotal setae, most are of medium size and barbed; the nymphs have 15 pairs, most are short and smooth. In all juveniles, the setae of c-series are inserted on unsclerotized integument. In the larva, the pygidial shield is absent but, in the nymphs, the gastronotal shield is present and the setae p2 and p3 are inserted on unsclerotized integument. In the larva, a humeral organ is absent but is present in the nymphs.