在普通花园实验中,城市青蛙较高的性别反转率表明适应性微进化

IF 3.5 2区 生物学 Q1 EVOLUTIONARY BIOLOGY
Veronika Bókony, Emese Balogh, Zsanett Mikó, Andrea Kásler, Zoltán Örkényi, Nikolett Ujhegyi
{"title":"在普通花园实验中,城市青蛙较高的性别反转率表明适应性微进化","authors":"Veronika Bókony,&nbsp;Emese Balogh,&nbsp;Zsanett Mikó,&nbsp;Andrea Kásler,&nbsp;Zoltán Örkényi,&nbsp;Nikolett Ujhegyi","doi":"10.1111/eva.70093","DOIUrl":null,"url":null,"abstract":"<p>Ectothermic vertebrates with genotypic sex determination may adjust their sexual phenotype to early-life environmental conditions by sex reversal, and theoretical models predict diverse consequences for population dynamics and microevolution under environmental change. Environments that frequently expose individuals to sex-reversing effects may select for or against the propensity to undergo sex reversal, depending on the relative fitness of sex-reversed individuals. Yet, empirical data on the adaptive value and evolutionary potential of sex reversal is scarce. Here we conducted a common-garden experiment with agile frogs (<i>Rana dalmatina</i>) that respond to larval heat stress by sex reversal, to test whether sex-reversal propensity has changed via microevolution in populations that live in anthropogenic habitats where potentially sex-reversing heat events are more frequent, compared to populations that live in cooler woodland habitats. Furthermore, to infer the adaptive value of sex reversal, we compared fitness-related traits between heat-exposed genotypic females that phenotypically developed into males (sex-reversed) or females (sex-concordant). We found that the frequency of sex reversal varied between sibgroups and was higher in the sibgroups originating from anthropogenic habitats, regardless of the thermal environment they had been exposed to during the larval sex-determination period. Among heat-exposed animals, time to metamorphosis was similar between sex-reversed individuals and sex-concordant females, but the former reached larger body mass by the end of the experiment than the latter, approaching the mass of sex-concordant males. These results suggest that sex-reversal propensity may have increased in anthropogenic environments by adaptive microevolution, potentially to minimize the fitness cost of reduced growth caused by heat events. Thus, environmental sex reversal has the potential to provide an adaptive strategy for ectothermic vertebrates to cope with challenges of the Anthropocene. Such knowledge on the causes and consequences of sex reversal will help pinpoint which populations are most threatened by extinction due to climatically influenced sex determination.</p>","PeriodicalId":168,"journal":{"name":"Evolutionary Applications","volume":"18 4","pages":""},"PeriodicalIF":3.5000,"publicationDate":"2025-04-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/eva.70093","citationCount":"0","resultStr":"{\"title\":\"Higher Sex-Reversal Rate of Urban Frogs in a Common-Garden Experiment Suggests Adaptive Microevolution\",\"authors\":\"Veronika Bókony,&nbsp;Emese Balogh,&nbsp;Zsanett Mikó,&nbsp;Andrea Kásler,&nbsp;Zoltán Örkényi,&nbsp;Nikolett Ujhegyi\",\"doi\":\"10.1111/eva.70093\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Ectothermic vertebrates with genotypic sex determination may adjust their sexual phenotype to early-life environmental conditions by sex reversal, and theoretical models predict diverse consequences for population dynamics and microevolution under environmental change. Environments that frequently expose individuals to sex-reversing effects may select for or against the propensity to undergo sex reversal, depending on the relative fitness of sex-reversed individuals. Yet, empirical data on the adaptive value and evolutionary potential of sex reversal is scarce. Here we conducted a common-garden experiment with agile frogs (<i>Rana dalmatina</i>) that respond to larval heat stress by sex reversal, to test whether sex-reversal propensity has changed via microevolution in populations that live in anthropogenic habitats where potentially sex-reversing heat events are more frequent, compared to populations that live in cooler woodland habitats. Furthermore, to infer the adaptive value of sex reversal, we compared fitness-related traits between heat-exposed genotypic females that phenotypically developed into males (sex-reversed) or females (sex-concordant). We found that the frequency of sex reversal varied between sibgroups and was higher in the sibgroups originating from anthropogenic habitats, regardless of the thermal environment they had been exposed to during the larval sex-determination period. Among heat-exposed animals, time to metamorphosis was similar between sex-reversed individuals and sex-concordant females, but the former reached larger body mass by the end of the experiment than the latter, approaching the mass of sex-concordant males. These results suggest that sex-reversal propensity may have increased in anthropogenic environments by adaptive microevolution, potentially to minimize the fitness cost of reduced growth caused by heat events. Thus, environmental sex reversal has the potential to provide an adaptive strategy for ectothermic vertebrates to cope with challenges of the Anthropocene. Such knowledge on the causes and consequences of sex reversal will help pinpoint which populations are most threatened by extinction due to climatically influenced sex determination.</p>\",\"PeriodicalId\":168,\"journal\":{\"name\":\"Evolutionary Applications\",\"volume\":\"18 4\",\"pages\":\"\"},\"PeriodicalIF\":3.5000,\"publicationDate\":\"2025-04-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1111/eva.70093\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Evolutionary Applications\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/eva.70093\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"EVOLUTIONARY BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Evolutionary Applications","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/eva.70093","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"EVOLUTIONARY BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

具有基因型性别决定的外温脊椎动物可能会通过性别逆转来调整其性表型以适应生命早期的环境条件,理论模型预测了环境变化对种群动态和微进化的不同影响。经常使个体暴露于性别逆转效应的环境可能会根据性别逆转个体的相对适合度,选择支持或反对性别逆转的倾向。然而,有关性别逆转的适应价值和进化潜力的经验数据却很少。在这里,我们用敏捷蛙(Rana dalmatina)进行了一个普通花园实验,这种蛙通过性别逆转来应对幼虫热应激,与生活在较凉爽的林地栖息地的种群相比,生活在可能导致性别逆转的热事件更频繁发生的人为栖息地的种群是否通过微进化改变了性别逆转倾向。此外,为了推断性别逆转的适应价值,我们比较了表型上发育成雄性(性别逆转)或雌性(性别一致)的受热基因型雌性动物之间的适应性相关特征。我们发现,性别逆转的频率在不同的同胞组之间存在差异,而在来自人为栖息地的同胞组中,性别逆转的频率较高,与它们在幼虫性别决定期所处的热环境无关。在暴露于热环境的动物中,性别逆转个体和性别一致的雌性个体的变态时间相似,但前者在实验结束时的体重大于后者,接近性别一致的雄性个体的体重。这些结果表明,在人类活动的环境中,性别逆转的倾向可能会通过适应性微进化而增加,这可能是为了最大限度地降低热事件导致的生长减少所带来的健康代价。因此,环境性别逆转有可能为外温脊椎动物提供一种适应策略,以应对人类世的挑战。了解性别逆转的原因和后果将有助于确定哪些种群因受气候影响的性别决定而面临最大的灭绝威胁。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Higher Sex-Reversal Rate of Urban Frogs in a Common-Garden Experiment Suggests Adaptive Microevolution

Higher Sex-Reversal Rate of Urban Frogs in a Common-Garden Experiment Suggests Adaptive Microevolution

Ectothermic vertebrates with genotypic sex determination may adjust their sexual phenotype to early-life environmental conditions by sex reversal, and theoretical models predict diverse consequences for population dynamics and microevolution under environmental change. Environments that frequently expose individuals to sex-reversing effects may select for or against the propensity to undergo sex reversal, depending on the relative fitness of sex-reversed individuals. Yet, empirical data on the adaptive value and evolutionary potential of sex reversal is scarce. Here we conducted a common-garden experiment with agile frogs (Rana dalmatina) that respond to larval heat stress by sex reversal, to test whether sex-reversal propensity has changed via microevolution in populations that live in anthropogenic habitats where potentially sex-reversing heat events are more frequent, compared to populations that live in cooler woodland habitats. Furthermore, to infer the adaptive value of sex reversal, we compared fitness-related traits between heat-exposed genotypic females that phenotypically developed into males (sex-reversed) or females (sex-concordant). We found that the frequency of sex reversal varied between sibgroups and was higher in the sibgroups originating from anthropogenic habitats, regardless of the thermal environment they had been exposed to during the larval sex-determination period. Among heat-exposed animals, time to metamorphosis was similar between sex-reversed individuals and sex-concordant females, but the former reached larger body mass by the end of the experiment than the latter, approaching the mass of sex-concordant males. These results suggest that sex-reversal propensity may have increased in anthropogenic environments by adaptive microevolution, potentially to minimize the fitness cost of reduced growth caused by heat events. Thus, environmental sex reversal has the potential to provide an adaptive strategy for ectothermic vertebrates to cope with challenges of the Anthropocene. Such knowledge on the causes and consequences of sex reversal will help pinpoint which populations are most threatened by extinction due to climatically influenced sex determination.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Evolutionary Applications
Evolutionary Applications 生物-进化生物学
CiteScore
8.50
自引率
7.30%
发文量
175
审稿时长
6 months
期刊介绍: Evolutionary Applications is a fully peer reviewed open access journal. It publishes papers that utilize concepts from evolutionary biology to address biological questions of health, social and economic relevance. Papers are expected to employ evolutionary concepts or methods to make contributions to areas such as (but not limited to): medicine, agriculture, forestry, exploitation and management (fisheries and wildlife), aquaculture, conservation biology, environmental sciences (including climate change and invasion biology), microbiology, and toxicology. All taxonomic groups are covered from microbes, fungi, plants and animals. In order to better serve the community, we also now strongly encourage submissions of papers making use of modern molecular and genetic methods (population and functional genomics, transcriptomics, proteomics, epigenetics, quantitative genetics, association and linkage mapping) to address important questions in any of these disciplines and in an applied evolutionary framework. Theoretical, empirical, synthesis or perspective papers are welcome.
×
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