亲缘关系在多个空间尺度上影响黑鳍鲨(Carcharhinus limbatus)的遗传种群结构

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Dominic G. Swift, Shannon J. O'Leary, R. Dean Grubbs, Bryan S. Frazier, Andrew T. Fields, Jayne M. Gardiner, J. Marcus Drymon, Dana M. Bethea, Tonya R. Wiley, David S. Portnoy
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引用次数: 1

摘要

了解微进化力量之间的相互作用如何产生被开发物种的遗传群体结构,对于实施促进持久性的管理政策至关重要。许多沿海鲨鱼物种表现出的亲缘关系可以影响基因流动和促进选择,并对空间尺度的管理有直接的影响。本研究采用混合标记方法对黑鳍鲨(Carcharhinus limbatus)的遗传结构进行了研究,该方法采用线粒体控制区序列和使用ddRAD-Seq生成的4339个含有snp的位点。在包括墨西哥湾在内的美国北大西洋西部水域的11个地点取样的年度年轻样本进行了遗传变异评估。空间和环境分析检测到68个核位点在选择下,可以对中性和适应性遗传结构进行单独评估。线粒体和中性SNP数据都表明了三个基因上不同的单位——大西洋、东海湾和西海湾——与区域种群一致,表明了男性和女性的区域偏好。在海湾单位内的不同地点中,观察到与温度和盐度相关的选择位点的异质性,表明局部适应。此外,在同一地点发现了5对兄弟姐妹,其时间尺度与女性生殖周期相对应。这表明雌性重复使用一个地点进行分娩,这有可能促进相邻地点之间适应性变异的分类。结果表明,微进化力在不同空间尺度上的不同影响,并强调了保护基本栖息地对维持物种适应变异来源的重要性,这可能缓冲物种对环境变化的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Philopatry influences the genetic population structure of the blacktip shark (Carcharhinus limbatus) at multiple spatial scales

Understanding how interactions among microevolutionary forces generate genetic population structure of exploited species is vital to the implementation of management policies that facilitate persistence. Philopatry displayed by many coastal shark species can impact gene flow and facilitate selection, and has direct implications for the spatial scales of management. Here, genetic structure of the blacktip shark (Carcharhinus limbatus) was examined using a mixed-marker approach employing mitochondrial control region sequences and 4339 SNP-containing loci generated using ddRAD-Seq. Genetic variation was assessed among young-of-the-year sampled in 11 sites in waters of the United States in the western North Atlantic Ocean, including the Gulf of Mexico. Spatial and environmental analyses detected 68 nuclear loci putatively under selection, enabling separate assessments of neutral and adaptive genetic structure. Both mitochondrial and neutral SNP data indicated three genetically distinct units—the Atlantic, eastern Gulf, and western Gulf—that align with regional stocks and suggest regional philopatry by males and females. Heterogeneity at loci putatively under selection, associated with temperature and salinity, was observed among sites within Gulf units, suggesting local adaptation. Furthermore, five pairs of siblings were identified in the same site across timescales corresponding with female reproductive cycles. This indicates that females re-used a site for parturition, which has the potential to facilitate the sorting of adaptive variation among neighbouring sites. The results demonstrate differential impacts of microevolutionary forces at varying spatial scales and highlight the importance of conserving essential habitats to maintain sources of adaptive variation that may buffer species against environmental change.

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来源期刊
Molecular Ecology
Molecular Ecology 生物-进化生物学
CiteScore
8.40
自引率
10.20%
发文量
472
审稿时长
1 months
期刊介绍: Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include: * population structure and phylogeography * reproductive strategies * relatedness and kin selection * sex allocation * population genetic theory * analytical methods development * conservation genetics * speciation genetics * microbial biodiversity * evolutionary dynamics of QTLs * ecological interactions * molecular adaptation and environmental genomics * impact of genetically modified organisms
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