Effects of glaciation and whole genome duplication on the distribution of the Campanula rotundifolia polyploid complex ...
Premise Of The Study Both intrinsic and extrinsic factors contribute to a species distribution. Among plants, the extrinsic effects of glaciation and intrinsic effects of whole genome duplication are powerful drivers of biogeographical patterns, but the interplay of these factors is poorly understoo...
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| Format: | Dataset |
| Language: | English |
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Dryad
2021
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| Online Access: | https://dx.doi.org/10.5061/dryad.hqbzkh1gp https://datadryad.org/stash/dataset/doi:10.5061/dryad.hqbzkh1gp |
| Summary: | Premise Of The Study Both intrinsic and extrinsic factors contribute to a species distribution. Among plants, the extrinsic effects of glaciation and intrinsic effects of whole genome duplication are powerful drivers of biogeographical patterns, but the interplay of these factors is poorly understood. Here, we investigate the roles glaciation and whole-genome duplication have played in the evolution of the widespread polyploid complex Campanula rotundifolia. Methods We assessed the cytotype of 37 populations that spanned the geographic and cytotypic range of the C. rotundifolia complex. We constructed a chloroplast phylogeny for these populations and used RAD-seq to create nuclear phylogenies and networks for a subset of 23 populations; and estimated divergence times of major clades using Bayesian estimation of substitution rates. Key Results Campanula rotundifolia originated in south-central Europe and underwent range expansion throughout much of Europe and North America. Multiple genome duplications have ... : This dataset consists of two DNA sequence alignments, one nuclear sdRAD DNA, one chloroplast DNA. All individual sequences are also archived in NCBI. Nuclear RADseq sequences are in the SRA archive (Accession SRP151156) and chloroplast sequences are in GenBank (Accessions: MH509220 – MH509381). RADseq data was generated for 26 pooled populations (6-10 individuals / population) using the SacI restriction enzyme and sequenced on an Illumina HiSeq 2500. Chloroplast sequences were generated using Sanger sequencing for up to three individuals per 37 populations. Chloroplast sequences were aligned using CodonCode Aligner and proofread by hand. RADseq sequences were first screened using Stacks for SNPs that varied between populations but were fixed within populations, because we sequenced pooled data. These retained reads were than concatenated into one sequence by population and aligned. ... |
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