ddRAD (quaddRAD) data of bumblebees
Data files
Sep 21, 2023 version files 16.98 MB
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ALL_SITES_650772.vcf.gz
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README.md
Abstract
Insect pollination is fundamental for natural ecosystems and agricultural crops. The bumblebee species Bombus terrestris has become a popular choice for commercial crop pollination worldwide due to its effectiveness and ease of mass rearing. Bumblebee colonies are mass-produced for the pollination of more than 20 crops and imported into over 50 countries including countries outside their native ranges, and the risk of invasion by commercial non-native bumblebees is considered as an emerging issue for global conservation and biological diversity. Here we use genome-wide data from seven wild populations close to and far from farms using commercial colonies, as well as commercial populations, to investigate the implications of utilising commercial bumblebee subspecies in the UK. We find evidence for generally low levels of introgression between commercial and wild bees, with higher admixture proportions in the bees occurring close to farms. We identify genomic regions putatively involved in local and global adaptation, and genes in locally adaptive regions were found to be enriched for functions related to taste receptor activity, oxidoreductase activity, fatty acid and lipid biosynthetic processes. Despite more than 30 years of bumblebee colony importation into the UK, we observe low impact on the genetic integrity of local B. terrestris populations, but we highlight that even limited introgression might negatively affect locally adapted alleles.
README: ddRAD (quaddRAD) data of bumblebees
https://doi.org/10.5061/dryad.5tb2rbp9r
Description of the data and file structure
This is a VCF file containing a total of 125 individual bumblebees. After genotype calling and filtering according to the criteria detailed in the manuscript (see Materials and Methods section), a matrix of 650,772 loci (including 8,953 variants, of which 6,774 had reduced linkage between nearby sites) was retained for downstream genomic analyses.
Methods
DNA was extracted from whole body and individual quaddRAD libraries were prepared and sequenced in Illumina HiSeq2500.