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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

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Abstract

Since 2005, the population of the trans-border brown bear (Ursus arctos) in Trilateral Park Pasvik-Inari (Norway-Finland-Russia) has been monitored by using genetic analyses of hair and faeces collected randomly in the field. A more systematic method using hair traps every fourth year was initiated in 2007 to collect brown bear hairs for genetic analysis. The method consisted of 56 hair traps in Norway, Finland and Russia in a 5 x 5 km2 grid cell system (ca 1400 km2). The project was repeated in 2011, 2015, 2019 and now in 2023. This season’s sampling was carried out in Pasvik (Norway) - Inari (Finland) area (43 squares, 1075 km2), using the same methodology as in the previous studies. A total of 97 samples were collected, where 45 samples came from Finland and 52 samples from Norway. In the bear specific analysis, 71 (73 %) of the 97 hair samples were positive. A complete DNA profile could be determined for 63 of the positive samples. In total, 22 different bear individuals were detected (10 females and 12 males). Of these 22 bears, 12 bears were detected in previous years, while 10 were previously unknown bears. In total, 13 bears were detected in Finland and 11 bears in Norway. This year’s sampling has the 2nd highest success rate in number of individuals detected per grid square, with 0,51 individual per grid square compared to 0,81 individuals in 2019 (highest success rate), 0,49 in 2015, 0,35 in 2011 and 0,42 in 2009. Our results showed that even with a smaller study area, the hair trap project every 4th year provides valuable information on the brown bear individuals in addition to a random sampling in the field (The National Monitoring Program for brown bears in Norway).

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Abstract

Aim Effective management of non-indigenous species requires knowledge of their dispersal factors and founder events. We aim to identify the main environmental drivers favouring dispersal events along the invasion gradient and to characterize the spatial patterns of genetic diversity in feral populations of the non-native pink salmon within its epicentre of invasion in Norway. Location Mainland Norway and North Atlantic Basin. Methods We first conducted SDM using four modelling techniques with varying levels of complexity, which encompassed both regression-based and tree-based machine-learning algorithms, using climatic data from the present to 2050. Then, we used the triple-enzyme restriction-site associated DNA sequencing (3RADseq) approach to genotype over 30,000 high-quality single-nucleotide polymorphisms to elucidate the patterns of genetic diversity and gene flow within the pink salmon putative invasion hotspot. Results We discovered temperature- and precipitation-related variables drove pink salmon distributional shifts across its non-native ranges and that climate-induced favourable areas will remain stable for the next 30 years. In addition, all SDMs identified north-eastern Norway as the epicentre of the pink salmon invasion, and genomic data revealed that there was minimal variation in genetic diversity across the sampled populations at a genome-wide level in this region. While utilizing a specific group of ‘diagnostic’ SNPs, we observed a significant degree of genetic differentiation, ranging from moderate to substantial, and detected four hierarchical genetic clusters concordant with geography. Main Conclusions Our findings suggest that fluctuations in climate extreme events associated with ongoing climate change will likely maintain environmental favourability for the pink salmon outside its ‘native’/introduced ranges. Locally invaded rivers are themselves potential source populations of invaders in the ongoing secondary spread of pink salmon in Northern Norway. Our study shows that SDMs and genomic data can reveal species distribution determinants and provide indicators to aid in post-control measures and potentially inferences about their success.

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Abstract

Here, we present, for the first time, the Ion TorrentⓇ next-generation sequencing (NGS) data for five houndsharks (Chondrichthyes: Triakidae), which include Galeorhinus galeus (number of bases pairs (bp) 17,487; GenBank accession number ON652874), Mustelus asterias (16,708; ON652873), Mustelus mosis (16,755; ON075077), Mustelus palumbes (16,708; ON075076), and Triakis megalopterus (16,746; ON075075). All assembled mitogenomes encode 13 protein-coding genes (PCGs), two ribosomal (r)RNA genes, and 22 transfer (t)RNA genes (tRNALeu and tRNASer are duplicated), except for G. galeus which contains 23 tRNA genes where tRNAThr is duplicated. The data presented in this paper can assist other researchers in further elucidating the diversification of triakid species and the phylogenetic relationships within Carcharhiniformes (groundsharks) as mitogenomes accumulate in public repositories.

Abstract

Background The order Lepidoptera has an abundance of species, including both agriculturally beneficial and detrimental insects. Molecular data has been used to investigate the phylogenetic relationships of major subdivisions in Lepidoptera, which has enhanced our understanding of the evolutionary relationships at the family and superfamily levels. However, the phylogenetic placement of many superfamilies and/or families in this order is still unknown. In this study, we determine the systematic status of the family Argyresthiidae within Lepidoptera and explore its phylogenetic affinities and implications for the evolution of the order. We describe the first mitochondrial (mt) genome from a member of Argyresthiidae, the apple fruit moth Argyresthia conjugella. The insect is an important pest on apples in Fennoscandia, as it switches hosts when the main host fails to produce crops. Results The mt genome of A. conjugella contains 16,044 bp and encodes all 37 genes commonly found in insect mt genomes, including 13 protein-coding genes (PCGs), two ribosomal RNAs, 22 transfer RNAs, and a large control region (1101 bp). The nucleotide composition was extremely AT-rich (82%). All detected PCGs (13) began with an ATN codon and terminated with a TAA stop codon, except the start codon in cox1 is ATT. All 22 tRNAs had cloverleaf secondary structures, except trnS1, where one of the dihydrouridine (DHU) arms is missing, reflecting potential differences in gene expression. When compared to the mt genomes of 507 other Lepidoptera representing 18 superfamilies and 42 families, phylogenomic analyses found that A. conjugella had the closest relationship with the Plutellidae family (Yponomeutoidea-super family). We also detected a sister relationship between Yponomeutoidea and the superfamily Tineidae. Conclusions Our results underline the potential importance of mt genomes in comparative genomic analyses of Lepidoptera species and provide valuable evolutionary insight across the tree of Lepidoptera species.