Data from: The pipid root

The estimation of phylogenetic relationships is an essential component of understanding evolution. Accurate phylogenetic estimation is difficult, however, when internodes are short and old, when genealogical discordance is common due to large ancestral effective population sizes or ancestral population structure, and when homoplasy is prevalent. Inference of divergence times is also hampered by unknown and uneven rates of evolution, the incomplete fossil record, uncertainty in relationships between fossil and extant lineages, and uncertainty in the age of fossils. Ideally these challenges can be overcome by developing large "phylogenomic" datasets, and by analyzing them with methods that accommodate features of the evolutionary process such as genealogical discordance, recurrent substitution, recombination, ancestral population structure, gene flow after speciation among sampled and unsampled taxa, and variation in evolutionary rates. In some phylogenetic problems it is possible to use information that is independent of fossils, such as the geological record, to identify putative triggers for diversification whose associated estimated divergence times can then be compared a posteriori to estimated relationships and ages of fossils. The history of diversification of pipid frog genera Pipa, Hymenochirus, Silurana, and Xenopus, for instance, is characterized by many of these evolutionary and analytical challenges. These frogs diversified dozens of millions of years ago, they have a relatively rich fossil record, their distributions span continental plates with a well characterized geological record of ancient connectivity, and there is considerable disagreement across studies in estimated evolutionary relationships. We used high throughput sequencing and public databases to generate a large phylogenomic dataset with which we estimated evolutionary relationships using multilocus coalescence methods. We collected sequence data from Pipa, Hymenochirus, Silurana, and Xenopus and the outgroup taxon Rhinophrynus dorsalis from coding sequence of 113 autosomal regions, averaging ~300 base pairs in length (range: 102 – 1695 base pairs), and also a portion of the mitochondrial genome. Analysis of these data using multiple approaches recovers strong support for the ((Xenopus, Silurana)(Pipa, Hymenochirus)) topology, and geologically calibrated divergence time estimates that are consistent with estimated ages and phylogenetic affinities of many fossils. These results provide new insights into the biogeography and chronology of pipid diversification during the breakup of Gondwanaland, and illustrate how phylogenomic data may be necessary to tackle tough problems in molecular systematics.Supplementary Information including accession numbersSuppl_Info.pdf*BEAST input file Pipa calibration JC codon modelpiponly_jc.xml*BEAST input file Pipa calibration HKY codon modelpiponly_hky.xml*BEAST input file Pipa calibration GTR codon modelpiponly_gtr.xml*BEAST input file Root calibration JC codon modelrootonly_jc.xml*BEAST input file Root calibration HKY codon modelrootonly_hky.xml*BEAST input file Root calibration GTR codon modelrootonly_gtr.xml*BEAST input file Pipa and Root calibration JC codon modelpipandroot_jc.xml*BEAST input file Pipa and Root calibration HKY codon modelpipandroot_hky.xml*BEAST input file Pipa and Root calibration GTR codon modelpipandroot_gtr.xmlBEST input file JC modelBEST_pipid_JC_114.inBEST input file HKY modelBEST_pipid_HKY_114.inBEST input file GTR modelBEST_pipid_GTR_114.i