Habitat Specialisation Impacts Clownfish Demographic Resilience to Pleistocene Sea-Level Fluctuations.

IF 3.9 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Alberto García-Jiménez, Marion Talbi, Lucy M Fitzgerald, A Heim, Anna Marcionetti, Sarah Schmid, Joris Bertrand, Abigail Shaughnessy, Carl Santiago, Ploypallin Rangseethampanya, Phurinat Ruttanachuchote, Wiphawan Aunkhongthong, Sittiporn Pengsakun, Makamas Sutthacheep, Milan Malinsky, Bruno Frédérich, Fabio Cortesi, Marc Kochzius, Thamasak Yeemin, Théo Gaboriau, Nicolas Salamin
{"title":"Habitat Specialisation Impacts Clownfish Demographic Resilience to Pleistocene Sea-Level Fluctuations.","authors":"Alberto García-Jiménez, Marion Talbi, Lucy M Fitzgerald, A Heim, Anna Marcionetti, Sarah Schmid, Joris Bertrand, Abigail Shaughnessy, Carl Santiago, Ploypallin Rangseethampanya, Phurinat Ruttanachuchote, Wiphawan Aunkhongthong, Sittiporn Pengsakun, Makamas Sutthacheep, Milan Malinsky, Bruno Frédérich, Fabio Cortesi, Marc Kochzius, Thamasak Yeemin, Théo Gaboriau, Nicolas Salamin","doi":"10.1111/mec.70134","DOIUrl":null,"url":null,"abstract":"<p><p>Habitat fragmentation and loss are key threats to biodiversity, yet their impacts on marine species remain poorly understood. Clownfishes, which rely on sea anemones for shelter and reproduction, provide an interesting model to explore how ecological specialisation mediates species responses to habitat perturbations. We used whole-genome data from 382 individuals across 10 species with varying host specialisations to reconstruct demographic histories and infer spatial genetic structure to assess the impact of Pleistocene sea-level fluctuations. Generalist species, associated with multiple hosts, maintained stable effective population sizes ( <math> <semantics> <mrow><msub><mi>N</mi> <mi>e</mi></msub> </mrow> <annotation>$$ {N}_e $$</annotation></semantics> </math> ) and population connectivity during habitat fragmentation, reflecting resilience to environmental instability. In contrast, specialists experienced severe <math> <semantics> <mrow><msub><mi>N</mi> <mi>e</mi></msub> </mrow> <annotation>$$ {N}_e $$</annotation></semantics> </math> declines and genetic structuring, driven by their dependence on specific hosts, without signs of population recovery following habitat reconnection. Spatial genomic analyses identified the Indonesian Through-Flow as a key dispersal corridor and the Coral Triangle as a critical hub of genetic diversity, while continental shelves and extensive open ocean regions appeared as barriers to gene flow. Our findings reveal how host specialisation shapes clownfish population dynamics, emphasising the importance of incorporating ecological dependencies into conservation assessments and deepening our understanding of species responses to ecological constraints and environmental changes over evolutionary timescales.</p>","PeriodicalId":210,"journal":{"name":"Molecular Ecology","volume":" ","pages":"e70134"},"PeriodicalIF":3.9000,"publicationDate":"2025-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Ecology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/mec.70134","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Habitat fragmentation and loss are key threats to biodiversity, yet their impacts on marine species remain poorly understood. Clownfishes, which rely on sea anemones for shelter and reproduction, provide an interesting model to explore how ecological specialisation mediates species responses to habitat perturbations. We used whole-genome data from 382 individuals across 10 species with varying host specialisations to reconstruct demographic histories and infer spatial genetic structure to assess the impact of Pleistocene sea-level fluctuations. Generalist species, associated with multiple hosts, maintained stable effective population sizes ( N e $$ {N}_e $$ ) and population connectivity during habitat fragmentation, reflecting resilience to environmental instability. In contrast, specialists experienced severe N e $$ {N}_e $$ declines and genetic structuring, driven by their dependence on specific hosts, without signs of population recovery following habitat reconnection. Spatial genomic analyses identified the Indonesian Through-Flow as a key dispersal corridor and the Coral Triangle as a critical hub of genetic diversity, while continental shelves and extensive open ocean regions appeared as barriers to gene flow. Our findings reveal how host specialisation shapes clownfish population dynamics, emphasising the importance of incorporating ecological dependencies into conservation assessments and deepening our understanding of species responses to ecological constraints and environmental changes over evolutionary timescales.

栖息地特化影响小丑鱼种群对更新世海平面波动的适应能力。
栖息地破碎化和丧失是对生物多样性的主要威胁,但它们对海洋物种的影响仍知之甚少。小丑鱼依靠海葵来庇护和繁殖,为探索生态特化如何调节物种对栖息地扰动的反应提供了一个有趣的模型。我们使用了来自10个不同寄主特化物种的382个个体的全基因组数据来重建人口历史并推断空间遗传结构,以评估更新世海平面波动的影响。在栖息地破碎化过程中,与多个寄主相关的通才物种保持稳定的有效种群规模(N e $$ {N}_e $$)和种群连通性,反映了对环境不稳定的适应能力。相比之下,专家经历了严重的N e $$ {N}_e $$下降和遗传结构,这是由它们对特定宿主的依赖所驱动的,在栖息地重新连接后没有种群恢复的迹象。空间基因组分析确定印度尼西亚通流是一个关键的扩散走廊,珊瑚三角是一个关键的遗传多样性中心,而大陆架和广阔的开放海洋地区似乎是基因流动的障碍。我们的研究结果揭示了宿主专业化如何塑造小丑鱼种群动态,强调了将生态依赖性纳入保护评估的重要性,并加深了我们对物种在进化时间尺度上对生态约束和环境变化的反应的理解。
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
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
×
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:604180095
Book学术官方微信