Weak range-wide population structure in the blackfin tuna (Thunnus atlanticus) revealed by analysis of genome-wide SNPs

被引:3
作者
Dimens, Pavel [1 ]
Reynal, Lionel [2 ]
Pau, Cedric [2 ]
Arocha, Freddy [3 ]
Hazin, Fabio [4 ]
Roque, Pollyana [4 ]
Cummings, Nancie J. [5 ]
Franks, James S. [6 ]
Jones, Kenneth L. [7 ]
Saillant, Eric A. [1 ]
机构
[1] Univ Southern Mississippi, Sch Ocean Sci & Engn, Ocean Springs, MS 39564 USA
[2] IFREMER Delegat Martinique, F-97231 Le Robert, La Martinique, France
[3] Univ Oriente, Inst Oceanog Venezuela, Cumana 6101, Venezuela
[4] Univ Fed Rural Pernambuco, Fisheries & Aquaculture Dept, Dom Manoel Medeiros S-N, BR-52171900 Recife, Brazil
[5] Southeast Fisheries Ctr, 75 Virginia Beach Dr, Key Biscayne, FL 33149 USA
[6] Univ Southern Mississippi, Ctr Fisheries Res & Dev, Ocean Springs, MS 39564 USA
[7] Univ Oklahoma, Hlth Sci Ctr, Dept Cell Biol, 975 NE 10th St,BRC 458, Oklahoma City, OK 73104 USA
关键词
blackfin tuna; double-digest RAD sequencing; population genetics; single nucleotide polymorphism; stock structure; Thunnus atlanticus; SPATIAL AUTOCORRELATION ANALYSIS; LOCAL ADAPTATION; GENE FLOW; MARINE FISH; ADAPTIVE DIVERGENCE; INFERENCE; ALBACARES; SELECTION; DIFFERENTIATION; HAPLOTYPES;
D O I
10.1093/icesjms/fsad012
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Blackfin tuna (Thunnus atlanticus) is a small tuna distributed in the western Atlantic Ocean where it is exploited by growing recreational and commercial regional fisheries. In this work, genome-wide genetic variation was analysed to investigate the occurrence of stock subdivision. A de novo assembly of the blackfin tuna genome was generated using Illumina paired-end sequencing data and applied as a reference for population genomic analysis of specimens from nine localities (average sample size per locality n = 72) spanning most of the blackfin tuna distribution range. A total of 2139 single-nucleotide polymorphisms were discovered and genotyped using the double-digest restriction associated DNA sequencing. Pairwise exact homogeneity tests were significant in 24 out of 36 population pairs and significant spatial autocorrelation of genotypes was observed for specimens collected within 2250 km of each other. However, divergence among locality samples was very low (pairwise F-ST range 0.0002-0.0025) and significant temporal variations were detected in localities sampled multiple times. Approaches to detect cryptic groups de novo were unsuccessful. Additional sampling is warranted to determine if multiple stocks need to be defined for management and assess temporal and spatial patterns of gene flow connecting them.
引用
收藏
页码:941 / 952
页数:12
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