Affiliations 

  • 1 Museum and Institute of Zoology, Polish Academy of Sciences, Poland; School of Life Sciences, University of Lincoln, UK. Electronic address: avmoura@miiz.waw.pl
  • 2 School of Life Sciences, University of Lincoln, UK; Institute of Medical Sciences, School of Medical Sciences, University of Aberdeen, UK
  • 3 Museum and Institute of Zoology, Polish Academy of Sciences, Poland; School of Life Sciences, University of Lincoln, UK
  • 4 Institute for Bioinformatics and Evolutionary Studies (IBEST), University of Idaho, USA
  • 5 School of Biosciences, Durham University, UK
  • 6 Wildlife Research Center, Kyoto University, Japan
  • 7 College of Science and Engineering, Flinders University, Australia
  • 8 College of Natural and Health Sciences, Zayed University, United Arab Emirates
  • 9 Consiglio Nazionale delle Ricerche-Istituto di Scienze Marine, Ancona, Italy
  • 10 Smithsonian National Museum of Natural History, USA
  • 11 Division of Science, Yale-NUS College, Singapore
  • 12 Marine Conservation International, UK
  • 13 School of Biosciences, Durham University, UK; Marine Scotland Science, Scottish Government, Marine Laboratory, UK
  • 14 Institute of Marine Science, University of Karachi, Pakistan
  • 15 Environment Society of Oman, Oman
  • 16 Ocean Giants Program, Wildlife Conservation Society, USA
  • 17 Five Oceans Environmental Services, Oman
  • 18 Megaptera Marine Conservation, Netherlands
  • 19 The MareCet Research Organization, Malaysia
  • 20 School of Biosciences, Durham University, UK. Electronic address: a.r.hoelzel@dur.ac.uk
Mol Phylogenet Evol, 2020 05;146:106756.
PMID: 32028032 DOI: 10.1016/j.ympev.2020.106756

Abstract

Phylogeographic inference has provided extensive insight into the relative roles of geographical isolation and ecological processes during evolutionary radiations. However, the importance of cross-lineage admixture in facilitating adaptive radiations is increasingly being recognised, and suggested as a main cause of phylogenetic uncertainty. In this study, we used a double digest RADseq protocol to provide a high resolution (~4 Million bp) nuclear phylogeny of the Delphininae. Phylogenetic resolution of this group has been especially intractable, likely because it has experienced a recent species radiation. We carried out cross-lineage reticulation analyses, and tested for several sources of potential bias in determining phylogenies from genome sampling data. We assessed the divergence time and historical demography of T. truncatus and T. aduncus by sequencing the T. aduncus genome and comparing it with the T. truncatus reference genome. Our results suggest monophyly for the genus Tursiops, with the recently proposed T. australis species falling within the T. aduncus lineage. We also show the presence of extensive cross-lineage gene flow between pelagic and European coastal ecotypes of T. truncatus, as well as in the early stages of diversification between spotted (Stenella frontalis; Stenella attenuata), spinner (Stenella longirostris), striped (Stenella coeruleoalba), common (Delphinus delphis), and Fraser's (Lagenodelphis hosei) dolphins. Our study suggests that cross-lineage gene flow in this group has been more extensive and complex than previously thought. In the context of biogeography and local habitat dependence, these results improve our understanding of the evolutionary processes determining the history of this lineage.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.