The importance of replicating genomic analyses to verify phylogenetic signal for recently evolved lineages

• Published in: Molecular Ecology
• Main Authors: Fraser, Ceridwen I., McGaughran, Angela, Chuah, Aaron, Waters, Jonathan M.
• Other Authors: Australian Research Council, University of Otago
• Format: Article in Journal/Newspaper
• Language: English
• Published: Wiley 2016
• Subjects: Genetics; Ecology, Evolution, Behavior and Systematics; Antarc*; Antarctica
• Online Access: http://dx.doi.org/10.1111/mec.13708; https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fmec.13708; https://onlinelibrary.wiley.com/doi/pdf/10.1111/mec.13708; https://onlinelibrary.wiley.com/doi/full-xml/10.1111/mec.13708; https://onlinelibrary.wiley.com/doi/am-pdf/10.1111/mec.13708

Abstract Genomewide SNP data generated by nontargeted methods such as RAD and GBS are increasingly being used in phylogenetic and phylogeographic analyses. When these methods are used in the absence of a reference genome, however, little is known about the locations and evolution of the SNP s. In using such data to address phylogenetic questions, researchers risk drawing false conclusions, particularly if a representative number of SNP s is not obtained. Here, we empirically test the robustness of phylogenetic inference based on SNP data for closely related lineages. We conducted a genomewide analysis of 75 712 SNP s, generated via GBS , of southern bull‐kelp ( Durvillaea ). Durvillaea chathamensis co‐occurs with D. antarctica on Chatham Island, but the two species have previously been found to be so genetically similar that the status of the former has been questioned. Our results show that D. chathamensis , which differs from D. antarctica ecologically as well as morphologically, is indeed a reproductively isolated species. Furthermore, our replicated analyses show that D. chathamensis cannot be reliably distinguished phylogenetically from closely related D. antarctica using subsets (ranging in size from 400 to 10 000 sites) of the 40 912 parsimony‐informative SNP s in our data set and that bootstrap values alone can give misleading impressions of the strength of phylogenetic inferences. These results highlight the importance of independently replicating SNP analyses to verify that phylogenetic inferences based on nontargeted SNP data are robust. Our study also demonstrates that modern genomic approaches can be used to identify cases of recent or incipient speciation that traditional approaches (e.g. Sanger sequencing of a few loci) may be unable to detect or resolve.