Data from: Genomics reveals the role of admixture in the evolution of structure among sperm whale populations within the Mediterranean Sea ...

In oceanic ecosystems, the nature of barriers to gene flow, and the processes by which populations may become isolated are different from the terrestrial environment, and less well understood. In this study, we investigate a highly mobile species (the sperm whale, Physeter macrocephalus) that is gen...

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Bibliographic Details
Main Authors: Violi, Biagio, De Jong, Menno, Frantzis, Alexandros, Alexiadou, Paraskevi, Tardy, Céline, Ody, Denis, De Stefanis, Renaud, Giménez Verdugo, Joan, Lucifora, Giuseppe, Silva, Mónica, Oliveira, Claudia, Alves, Filipe, Dinis, Ana, Tejedor, Marisa, Fernandez, Antonio, Arregui, Marina, Arbelo, Manuel, Lopez, Alfredo, Covelo, Pablo, Hoelzel, Rus
Format: Dataset
Language:English
Published: Dryad 2023
Subjects:
Kay
Online Access:https://dx.doi.org/10.5061/dryad.dv41ns233
https://datadryad.org/stash/dataset/doi:10.5061/dryad.dv41ns233
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Summary:In oceanic ecosystems, the nature of barriers to gene flow, and the processes by which populations may become isolated are different from the terrestrial environment, and less well understood. In this study, we investigate a highly mobile species (the sperm whale, Physeter macrocephalus) that is genetically differentiated between an open North Atlantic population and the populations in the Mediterranean Sea. We apply high-resolution single nucleotide polymorphisms (SNP) analysis to study the nature of barriers to gene flow in this system, comparing gene flow across the putative boundary into the Mediterranean (Strait of Gibraltar and Alboran Sea region) with novel analyses on structuring among sperm whale populations within the Mediterranean basin. Our data support a recent founding of the Mediterranean, around the time of the last glacial maximum, and shows concerted historical demographic profiles in both the Atlantic and the Mediterranean. In each region, there is evidence for a population decline around ... : Tissue samples were obtained during various research projects between 1999 and 2018. DNA was extracted both by kit (OMEGA BIOTEK and MN MACHEREY-NAGEL) following the manufacturer's protocol, and by the phenol chloroform method (after Hoelzel, 1998). Genomic DNA concentration was quantified using the Qubit High Sensitivity kit (Thermo Fisher Scientific). We applied the ddRADseq methodology (Peterson et al., 2012). Hoelzel, A. R. (1998) Molecular analysis of populations; a practical approach. Oxford, UK: Oxford University Press. Peterson, B. K., Weber, J. N., Kay, E. H., Fisher, H. S., & Hoekstra, H. E. (2012). Double digest RADseq: an inexpensive method for de novo SNP discovery and genotyping in model and non-model species. PloS one, 7(5), e37135. https://doi.org/10.1371/journal.pone.0037135 ...