FN Archimer Export Format
PT J
TI Seascape genomics reveals population isolation in the reef-building honeycomb worm, Sabellaria alveolata (L.)
BT 
AF Muir, Anna P.
   Dubois, Stanislas
   Ross, Rebecca E.
   Firth, Louise B.
   Knights, Antony M.
   Lima, Fernando P.
   Seabra, Rui
   Corre, Erwan
   Le Corguillé, Gildas
   Nunes, Flavia
AS 1:1,2;2:3;3:4,5;4:6;5:4;6:7;7:7;8:8;9:8;10:2,3;
FF 1:;2:PDG-ODE-DYNECO-LEBCO;3:;4:;5:;6:;7:;8:;9:;10:PDG-ODE-DYNECO-LEBCO;
C1 Conservation Biology Research Group, Department of Biological Sciences, University of Chester, Parkgate Road, Chester, CH1 4BJ, UK
   Laboratoire des Sciences de l’Environnement Marin, LEMAR UMR 6539 CNRS/UBO/IRD/Ifremer, Université de Brest (UBO), Université Européenne de Bretagne (UEB), Institut Universitaire Européen de la Mer (IUEM), 29280, Plouzané, France
   Ifremer, DYNECO, Laboratory of Coastal Benthic Ecology, F-29280, Plouzané, France
   Marine Biology and Ecology Research Centre, School of Biological and Marine Sciences, University of Plymouth, Plymouth, PL4 8AA, UK
   Institute of Marine Research, 1870 Nordnes, 5817, Bergen, Norway
   School of Biological and Marine Sciences, University of Plymouth, Plymouth, PL4 8AA, UK
   CIBIO/InBIO, Centro de Investigação em Biodiversidade e Recursos Genéticos, Universidade do Porto, Vairão, Portugal
   CNRS, Sorbonne Université, FR2424, ABiMS, Station Biologique de Roscoff, 29680, Roscoff, France
C2 UNIV CHESTER, UK
   UBO, FRANCE
   IFREMER, FRANCE
   UNIV PLYMOUTH, UK
   IMR (BERGEN), NORWAY
   UNIV PLYMOUTH, UK
   UNIV PORTO, PORTUGAL
   CNRS, FRANCE
SI BREST
SE PDG-ODE-DYNECO-LEBCO
UM LEMAR
IN WOS Ifremer UPR
   WOS Cotutelle UMR
   DOAJ
   copubli-france
   copubli-europe
   copubli-univ-france
IF 3.26
TC 4
UR https://archimer.ifremer.fr/doc/00643/75538/76445.pdf
   https://archimer.ifremer.fr/doc/00643/75538/76446.docx
LA English
DT Article
DE ;RADseq;Ocean circulation modelling;Adaptation;Marine invertebrate;Larval dispersal
AB ackground Under the threat of climate change populations can disperse, acclimatise or evolve in order to avoid fitness loss. In light of this, it is important to understand neutral gene flow patterns as a measure of dispersal potential, but also adaptive genetic variation as a measure of evolutionary potential. In order to assess genetic variation and how this relates to environment in the honeycomb worm (Sabellaria alveolata (L.)), a reef-building polychaete that supports high biodiversity, we carried out RAD sequencing using individuals from along its complete latitudinal range. Patterns of neutral population genetic structure were compared to larval dispersal as predicted by ocean circulation modelling, and outlier analyses and genotype-environment association tests were used to attempt to identify loci under selection in relation to local temperature data. Results We genotyped 482 filtered SNPs, from 68 individuals across nine sites, 27 of which were identified as outliers using BAYESCAN and ARLEQUIN. All outlier loci were potentially under balancing selection, despite previous evidence of local adaptation in the system. Limited gene flow was observed among reef-sites (FST = 0.28 ± 0.10), in line with the low dispersal potential identified by the larval dispersal models. The North Atlantic reef emerged as a distinct population and this was linked to high local larval retention and the effect of the North Atlantic Current on dispersal. Conclusions As an isolated population, with limited potential for natural genetic or demographic augmentation from other reefs, the North Atlantic site warrants conservation attention in order to preserve not only this species, but above all the crucial functional ecological roles that are associated with their bioconstructions. Our study highlights the utility of using seascape genomics to identify populations of conservation concern. 
PY 2020
PD AUG
SO Bmc Evolutionary Biology
SN 1471-2148
PU Springer Science and Business Media LLC
VL 20
IS 1
UT 000561220800001
DI 10.1186/s12862-020-01658-9
ID 75538
ER

EF