Disparate genetic divergence patterns in three corals across a pan-Pacific environmental gradient highlight species-specific adaptation

Author:

Voolstra Christian R.,Hume Benjamin C. C.,Armstrong Eric J.,Mitushasi Guinther,Porro Barbara,Oury Nicolas,Agostini Sylvain,Boissin Emilie,Poulain Julie,Carradec Quentin,Paz-García David A.,Zoccola Didier,Magalon Hélène,Moulin Clémentine,Bourdin Guillaume,Iwankow Guillaume,Romac Sarah,Banaigs Bernard,Boss Emmanuel,Bowler Chris,de Vargas Colomban,Douville Eric,Flores Michel,Furla Paola,Galand Pierre E.,Gilson Eric,Lombard Fabien,Pesant Stéphane,Reynaud Stéphanie,Sullivan Matthew B.,Sunagawa Shinichi,Thomas Olivier P.,Troublé Romain,Thurber Rebecca Vega,Wincker Patrick,Planes Serge,Allemand Denis,Forcioli Didier

Abstract

AbstractTropical coral reefs are among the most affected ecosystems by climate change and face increasing loss in the coming decades. Effective conservation strategies that maximize ecosystem resilience must be informed by the accurate characterization of extant genetic diversity and population structure together with an understanding of the adaptive potential of keystone species. Here we analyzed samples from the Tara Pacific Expedition (2016–2018) that completed an 18,000 km longitudinal transect of the Pacific Ocean sampling three widespread corals—Pocillopora meandrina, Porites lobata, and Millepora cf. platyphylla—across 33 sites from 11 islands. Using deep metagenomic sequencing of 269 colonies in conjunction with morphological analyses and climate variability data, we can show that despite a targeted sampling the transect encompasses multiple cryptic species. These species exhibit disparate biogeographic patterns and, most importantly, distinct evolutionary patterns in identical environmental regimes. Our findings demonstrate on a basin scale that evolutionary trajectories are species-specific and can only in part be predicted from the environment. This highlights that conservation strategies must integrate multi-species investigations to discern the distinct genomic footprints shaped by selection as well as the genetic potential for adaptive change.

Funder

University of Konstanz

Agence Nationale de la Recherche

JST Spring

Labex Signalife

IDEX UCAJedi

H2020 Marie Skłodowska-Curie Actions

Publisher

Springer Science and Business Media LLC

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3