Harvesting-induced evolution of collective risk-taking behavior and changes to the circadian system in a fish

Author:

Sbragaglia Valerio,López-Olmeda Jose Fernando,Frigato Elena,Bertolucci Cristiano,Arlinghaus Robert

Abstract

ABSTRACTIntensive and trait-selective harvesting of fish and wildlife can cause evolutionary changes in a range of life-history and behavioural traits. These changes might in turn alter the circadian system both at behavioral and molecular levels, with knock-on effects on daily physiological processes and behavioural outputs. We examined the evolutionary impact of size-selective mortality on collective risk-taking behavior and the circadian system in a model fish species. We exposed zebrafish (Danio rerio) to either large or small size-selective mortality relative to a control over five generations, followed by eight generations during which harvesting halted to remove maternal effects. Large size-selective mortality typical of many fisheries and specialized predators targeting larger size classes decreased collective risk-taking behavior compared to controls. The opposite occurred in response to small size-selective mortality typical of specialized fisheries and most gape-limited predators. The evolutionary changes in risk-taking behavior were linked to daily activity rhythms in response to small size-selective mortality, while no changes were observed in response to large size-selective mortality. We also found changes in the molecular circadian core clockwork in response to both size selective mortality treatments. These changes disappeared in the clock output pathway, resulting in similar transcription profiles of both size-selected lines. The results suggest a switch downstream to the molecular circadian core clockwork, leading to overall similar daily activity patterns across selection lines. Our experimental harvest left an evolutionary legacy in collective risktaking behavior and relatedly in the circadian system, both at behavioral and molecular levels. Changes to risk-sensitive behavior of exploited organisms can have far-reaching consequences for how space and time is used and may also affect catchability and natural predation.

Publisher

Cold Spring Harbor Laboratory

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