Literature DB >> 25297864

Ecological opportunities and specializations shaped genetic divergence in a highly mobile marine top predator.

Marie Louis1, Michael C Fontaine2, Jérôme Spitz3, Erika Schlund4, Willy Dabin3, Rob Deaville5, Florence Caurant6, Yves Cherel6, Christophe Guinet6, Benoit Simon-Bouhet6.   

Abstract

Environmental conditions can shape genetic and morphological divergence. Release of new habitats during historical environmental changes was a major driver of evolutionary diversification. Here, forces shaping population structure and ecotype differentiation ('pelagic' and 'coastal') of bottlenose dolphins in the North-east Atlantic were investigated using complementary evolutionary and ecological approaches. Inference of population demographic history using approximate Bayesian computation indicated that coastal populations were likely founded by the Atlantic pelagic population after the Last Glacial Maxima probably as a result of newly available coastal ecological niches. Pelagic dolphins from the Atlantic and the Mediterranean Sea likely diverged during a period of high productivity in the Mediterranean Sea. Genetic differentiation between coastal and pelagic ecotypes may be maintained by niche specializations, as indicated by stable isotope and stomach content analyses, and social behaviour. The two ecotypes were only weakly morphologically segregated in contrast to other parts of the World Ocean. This may be linked to weak contrasts between coastal and pelagic habitats and/or a relatively recent divergence. We suggest that ecological opportunity to specialize is a major driver of genetic and morphological divergence. Combining genetic, ecological and morphological approaches is essential to understanding the population structure of mobile and cryptic species.
© 2014 The Author(s) Published by the Royal Society. All rights reserved.

Entities:  

Keywords:  bottlenose dolphins; demographic history; ecological niches; morphology; population genetics

Mesh:

Substances:

Year:  2014        PMID: 25297864      PMCID: PMC4213618          DOI: 10.1098/rspb.2014.1558

Source DB:  PubMed          Journal:  Proc Biol Sci        ISSN: 0962-8452            Impact factor:   5.349


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