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Molecular Ecology · 2025 · Vol. 34 · Issue 19 · Wiley
Salmonids have a remarkable ability to form sympatric morphs after postglacial colonisation of freshwater lakes. These morphs often differ in morphology, feeding and spawning behaviour. Here, we explored the genetic basis of morph differentiation in Arctic charr ( n = 283) by first establishing a high‐quality reference genome and then using this in whole genome sequencing of distinct morphs present in two Norwegian and two Ice...
Conservation Genetics · 2024 · Vol. 25 · Issue 2 · Springer
Genetic diversity is fundamental to the adaptive potential and survival of species. Although its importance has long been recognized in science, it has a history of neglect within policy, until now. The new Global Biodiversity Framework recently adopted by the Convention on Biological Diversity, states that genetic diversity must be maintained at levels assuring adaptive potential of populations, and includes metrics for syste...
Molecular Ecology · 2024 · Vol. 33 · Issue 2 · Wiley
International policy recently adopted commitments to maintain genetic diversity in wild populations to secure their adaptive potential, including metrics to monitor temporal trends in genetic diversity – so‐called indicators. A national programme for assessing trends in genetic diversity was recently initiated in Sweden. Relating to this effort, we systematically assess contemporary genome‐wide temporal trends (40 years) in wi...
Conservation Genetics · 2023 · Vol. 24 · Issue 4 · Springer
Population extinction is ubiquitous in all taxa. Such extirpations can reduce intraspecific diversity, but the extent to which genetic diversity of surviving populations are affected remains largely unclear. A key concept in this context is the effective population size ( N e ), which quantifies the rate at which genetic diversity within populations is lost. N e was developed for single, isolated populations while many natural...
Molecular Ecology · 2022 · Vol. 31 · Issue 24 · Wiley
Genetic diversity is the basis for population adaptation and long‐term survival, yet rarely considered in biodiversity monitoring. One key issue is the need for useful and straightforward indicators of genetic diversity. We monitored genetic diversity over 40 years (1970–2010) in metapopulations of brown trout ( Salmo trutta ) inhabiting 27 small mountain lakes representing 10 lake systems in central Sweden using >1200 fish pe...
Molecular Ecology · 2022 · Vol. 31 · Issue 2 · Wiley
The sympatric existence of genetically distinguishable populations of the same species remains a puzzle in ecology. Coexisting salmonid fish populations are known from over 100 freshwater lakes. Most studies of sympatric populations have used limited numbers of genetic markers making it unclear if genetic divergence involves certain parts of the genome. We returned to the first reported case of salmonid sympatry, initially det...
Molecular Ecology · 2019 · Vol. 28 · Issue 8 · Wiley
Estimation of effective population size ( N e ) from genetic marker data is a major focus for biodiversity conservation because it is essential to know at what rates inbreeding is increasing and additive genetic variation is lost. But are these the rates assessed when applying commonly used N e estimation techniques? Here we use recently developed analytical tools and demonstrate that in the case of substructured populations t...
Molecular Ecology · 2018 · Vol. 27 · Issue 20 · Wiley
Sympatric populations are conspecific populations that coexist spatially. They are of interest in evolutionary biology by representing the potential first steps of sympatric speciation and are important to identify and monitor in conservation management. Reviewing the literature pertaining to sympatric populations, we find that most cases of sympatry appear coupled to phenotypic divergence, implying ease of detection. In compa...
Molecular Ecology · 2014 · Vol. 23 · Issue 1 · Wiley
The world faces a global fishing crisis. Wild marine fisheries comprise nearly 15% of all animal protein in the human diet, but, according to the U.N. Food and Agriculture Organization, nearly 60% of all commercially important marine fish stocks are overexploited, recovering, or depleted (FAO ; Fig. ). Some authors have suggested that the large population sizes of harvested marine fish make even collapsed populations resistant...
Conservation Biology · 2013 · Vol. 27 · Issue 2 · Wiley
The wolf (Canis lupus) is classified as endangered in Sweden by the Swedish Species Information Centre, which is the official authority for threat classification. The present population, which was founded in the early 1980s, descends from 5 individuals. It is isolated and highly inbred, and on average individuals are more related than siblings. Hunts have been used by Swedish authorities during 2010 and 2011 to reduce the popu...
Molecular Ecology · 2007 · Vol. 16 · Issue 6 · Wiley
Previous studies have reported higher levels of divergence for microsatellites than for allozymes in several species, suggested to reflect stabilizing selection on the allozymes. We compared the differentiation patterns of 11 allozyme and nine microsatellite loci using 679 spawning Atlantic herring ( Clupea harengus ) collected in the Baltic and North Seas to test for differential natural selection on these markers. Observed d...
Molecular Ecology · 2006 · Vol. 15 · Issue 8 · Wiley
Information on statistical power is critical when planning investigations and evaluating empirical data, but actual power estimates are rarely presented in population genetic studies. We used computer simulations to assess and evaluate power when testing for genetic differentiation at multiple loci through combining test statistics or P values obtained by four different statistical approaches, viz. Pearson's chi‐square, the lo...
Molecular Ecology · 2005 · Vol. 14 · Issue 7 · Wiley
The genetic relationships among 337 northern pike ( Esox lucius ) collected from the coastal zone of the central Baltic region and the Finnish islands of Åland were analysed using five microsatellite loci. Spatial structure was delineated using both traditional F ‐statistics and individually based approaches including spatial autocorrelation analysis. Our results indicate that the observed genotypic distribution is incompatibl...