Libin Zhou, Kimberley D Lemmen, Shuaiying Zhao, Steven A J Declerck
{"title":"Asymmetrical evolution of cross inhibition in zooplankton: insights from contrasting phosphorus limitation and salinization exposure sequences.","authors":"Libin Zhou, Kimberley D Lemmen, Shuaiying Zhao, Steven A J Declerck","doi":"10.1098/rspb.2024.3064","DOIUrl":null,"url":null,"abstract":"<p><p>Understanding the evolutionary responses of organisms to multiple stressors is crucial for predicting the ecological consequences of intensified anthropogenic activities. While previous studies have documented the effects of selection history on organisms' abilities to cope with new stressors, the impact of the sequence in which stressors occur on evolutionary outcomes remains less understood. In this study, we examined the evolutionary responses of a metazoan rotifer species to two prevalent freshwater stressors: nutrient limitation and increased salinization. We subjected rotifer populations with distinct selection histories (salt-adapted, low phosphorus-adapted and ancestral clones) to a reciprocal common garden experiment and monitored their population growth rates. Our results revealed an asymmetric evolutionary response to phosphorus (P) limitation and increased salinity. Specifically, adaptation to low P conditions reduced rotifer tolerance to increased salinity, whereas adaptation to saline conditions did not show such cross-inhibitory effects. Instead, the addition of moderate concentrations of salt enhanced the growth of the salt-adapted population in low P conditions, potentially as a consequence of evolved cross-tolerance. Our findings, therefore, underscore the importance of considering historical stressor regimes to improve our understanding and predictions of organismal responses to multiple stressors and also have significant implications for ecosystem management.</p>","PeriodicalId":20589,"journal":{"name":"Proceedings of the Royal Society B: Biological Sciences","volume":"292 2042","pages":"20243064"},"PeriodicalIF":3.8000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11881020/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Proceedings of the Royal Society B: Biological Sciences","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1098/rspb.2024.3064","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/5 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Understanding the evolutionary responses of organisms to multiple stressors is crucial for predicting the ecological consequences of intensified anthropogenic activities. While previous studies have documented the effects of selection history on organisms' abilities to cope with new stressors, the impact of the sequence in which stressors occur on evolutionary outcomes remains less understood. In this study, we examined the evolutionary responses of a metazoan rotifer species to two prevalent freshwater stressors: nutrient limitation and increased salinization. We subjected rotifer populations with distinct selection histories (salt-adapted, low phosphorus-adapted and ancestral clones) to a reciprocal common garden experiment and monitored their population growth rates. Our results revealed an asymmetric evolutionary response to phosphorus (P) limitation and increased salinity. Specifically, adaptation to low P conditions reduced rotifer tolerance to increased salinity, whereas adaptation to saline conditions did not show such cross-inhibitory effects. Instead, the addition of moderate concentrations of salt enhanced the growth of the salt-adapted population in low P conditions, potentially as a consequence of evolved cross-tolerance. Our findings, therefore, underscore the importance of considering historical stressor regimes to improve our understanding and predictions of organismal responses to multiple stressors and also have significant implications for ecosystem management.
期刊介绍:
Proceedings B is the Royal Society’s flagship biological research journal, accepting original articles and reviews of outstanding scientific importance and broad general interest. The main criteria for acceptance are that a study is novel, and has general significance to biologists. Articles published cover a wide range of areas within the biological sciences, many have relevance to organisms and the environments in which they live. The scope includes, but is not limited to, ecology, evolution, behavior, health and disease epidemiology, neuroscience and cognition, behavioral genetics, development, biomechanics, paleontology, comparative biology, molecular ecology and evolution, and global change biology.