Holistic view of the seascape dynamics and environment impact on macro-scale genetic connectivity of marine plankton populations.

Romuald Laso-Jadart, Michael O'Malley, Adam M Sykulski, Christophe Ambroise, Mohammed-Amin Madoui
{"title":"Holistic view of the seascape dynamics and environment impact on macro-scale genetic connectivity of marine plankton populations.","authors":"Romuald Laso-Jadart, Michael O'Malley, Adam M Sykulski, Christophe Ambroise, Mohammed-Amin Madoui","doi":"10.1186/s12862-023-02160-8","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Plankton seascape genomics studies have revealed different trends from large-scale weak differentiation to microscale structures. Previous studies have underlined the influence of the environment and seascape on species differentiation and adaptation. However, these studies have generally focused on a few single species, sparse molecular markers, or local scales. Here, we investigated the genomic differentiation of plankton at the macro-scale in a holistic approach using Tara Oceans metagenomic data together with a reference-free computational method.</p><p><strong>Results: </strong>We reconstructed the F<sub>ST</sub>-based genomic differentiation of 113 marine planktonic taxa occurring in the North and South Atlantic Oceans, Southern Ocean, and Mediterranean Sea. These taxa belong to various taxonomic clades spanning Metazoa, Chromista, Chlorophyta, Bacteria, and viruses. Globally, population genetic connectivity was significantly higher within oceanic basins and lower in bacteria and unicellular eukaryotes than in zooplankton. Using mixed linear models, we tested six abiotic factors influencing connectivity, including Lagrangian travel time, as proxies of oceanic current effects. We found that oceanic currents were the main population genetic connectivity drivers, together with temperature and salinity. Finally, we classified the 113 taxa into parameter-driven groups and showed that plankton taxa belonging to the same taxonomic rank such as phylum, class or order presented genomic differentiation driven by different environmental factors.</p><p><strong>Conclusion: </strong>Our results validate the isolation-by-current hypothesis for a non-negligible proportion of taxa and highlight the role of other physicochemical parameters in large-scale plankton genetic connectivity. The reference-free approach used in this study offers a new systematic framework to analyse the population genomics of non-model and undocumented marine organisms from a large-scale and holistic point of view.</p>","PeriodicalId":9127,"journal":{"name":"BMC Ecology and Evolution","volume":"23 1","pages":"46"},"PeriodicalIF":0.0000,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10472650/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Ecology and Evolution","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/s12862-023-02160-8","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Plankton seascape genomics studies have revealed different trends from large-scale weak differentiation to microscale structures. Previous studies have underlined the influence of the environment and seascape on species differentiation and adaptation. However, these studies have generally focused on a few single species, sparse molecular markers, or local scales. Here, we investigated the genomic differentiation of plankton at the macro-scale in a holistic approach using Tara Oceans metagenomic data together with a reference-free computational method.

Results: We reconstructed the FST-based genomic differentiation of 113 marine planktonic taxa occurring in the North and South Atlantic Oceans, Southern Ocean, and Mediterranean Sea. These taxa belong to various taxonomic clades spanning Metazoa, Chromista, Chlorophyta, Bacteria, and viruses. Globally, population genetic connectivity was significantly higher within oceanic basins and lower in bacteria and unicellular eukaryotes than in zooplankton. Using mixed linear models, we tested six abiotic factors influencing connectivity, including Lagrangian travel time, as proxies of oceanic current effects. We found that oceanic currents were the main population genetic connectivity drivers, together with temperature and salinity. Finally, we classified the 113 taxa into parameter-driven groups and showed that plankton taxa belonging to the same taxonomic rank such as phylum, class or order presented genomic differentiation driven by different environmental factors.

Conclusion: Our results validate the isolation-by-current hypothesis for a non-negligible proportion of taxa and highlight the role of other physicochemical parameters in large-scale plankton genetic connectivity. The reference-free approach used in this study offers a new systematic framework to analyse the population genomics of non-model and undocumented marine organisms from a large-scale and holistic point of view.

Abstract Image

Abstract Image

Abstract Image

海洋浮游生物种群宏观遗传连通性的景观动态和环境影响的整体观点。
背景:浮游生物基因组学研究揭示了从大规模弱分化到微尺度结构的不同趋势。以往的研究强调了环境和海景对物种分化和适应的影响。然而,这些研究通常集中在少数单一物种,稀疏的分子标记或局部尺度上。本文利用Tara Oceans的宏基因组数据和无参考的计算方法,在宏观尺度上对浮游生物的基因组分化进行了整体研究。结果:基于fst重建了北大西洋、南大西洋、南大洋和地中海的113个海洋浮游生物类群的基因组分化。这些分类群属于不同的分类分支,跨越后生动物、染色动物、绿藻、细菌和病毒。在全球范围内,海洋盆地内的种群遗传连通性显著高于浮游动物,细菌和单细胞真核生物的种群遗传连通性显著低于浮游动物。利用混合线性模型,我们测试了影响连通性的6个非生物因素,包括拉格朗日旅行时间,作为洋流效应的代理。我们发现,洋流与温度和盐度一起是主要的种群遗传连通性驱动因素。结果表明,在不同环境因子的驱动下,在门、纲、目等相同分类等级的浮游生物类群呈现出基因组分化的特征。结论:我们的研究结果验证了“电流隔离假说”,并强调了其他物理化学参数在大尺度浮游生物遗传连通性中的作用。本研究中使用的无参考方法为从大规模和整体的角度分析非模型和未记录的海洋生物的种群基因组学提供了一个新的系统框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信