2020
DOI: 10.1038/s41598-020-79720-1
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Demographic analyses of a new sample of haploid genomes from a Swedish population of Drosophila melanogaster

Abstract: European and African natural populations of Drosophila melanogaster have been the focus of several studies aiming at inferring demographic and adaptive processes based on genetic variation data. However, in these analyses little attention has been given to gene flow between African and European samples. Here we present a dataset consisting of 14 fully sequenced haploid genomes sampled from a natural population from the northern species range (Umeå, Sweden). We co-analyzed this new data with an African populati… Show more

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Cited by 15 publications
(22 citation statements)
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“…We decided to mimic the conditions of a typical summer day in Oulu, Finland (65° North) for two reasons. First, Drosophila melanogaster populate Northern Scandinavian regions in this latitude and overwinter here (e.g., 37 ). Second, from mid-May to the end of June day length varies from 19 to 22 h, and the rest of the “night” corresponds to civil twilight, where the sun does not set more than 6° below the horizon and general activities can be performed without artificial light (‘white nights’, maximum darkness between 1–3 lux).…”
Section: Resultsmentioning
confidence: 99%
“…We decided to mimic the conditions of a typical summer day in Oulu, Finland (65° North) for two reasons. First, Drosophila melanogaster populate Northern Scandinavian regions in this latitude and overwinter here (e.g., 37 ). Second, from mid-May to the end of June day length varies from 19 to 22 h, and the rest of the “night” corresponds to civil twilight, where the sun does not set more than 6° below the horizon and general activities can be performed without artificial light (‘white nights’, maximum darkness between 1–3 lux).…”
Section: Resultsmentioning
confidence: 99%
“…In our simulations, we simulated 436 gene trees within the fixed species tree (see below) and three different population sizes: 100,000 diploid individuals, 1,000,000 diploid individuals and 10,000,000 diploid individuals. The chosen population sizes for the simulations were based on known insect effective population sizes (Keightley et al 2015; Crossley et al 2019; Arguello et al 2019; Kapopoulou et al 2020) and were conservatively large to explore the potential effect.…”
Section: Methods and Datamentioning
confidence: 99%
“…In addition to 7 strains carrying In(3R)Payne, we randomly picked an equal number of strains with standard arrangement on the third chromosome and obtained the genomic data from Dryad (http://doi.org/10.5061/dryad.403b2). In addition to this European low-latitude sample from Portugal, we integrated phased sequencing data from 14 non-inverted strains from a highlatitude population in Umeå (Sweden) into our analyses, which were sequenced as haploid embryos (Kapopoulou et al 2020), similar to the African samples mentioned above. Kapun et al (2016a), Rane et al (2015) found that Australian flies from tropical Queensland (where the polymorphism is segregating) do not exhibit elevated genetic differentiation between inverted and standard karyotypes within the genomic region spanned by In(3R)Payne.…”
Section: Additional Sequencing Data From Other Continentsmentioning
confidence: 99%