猎物对受伤易受伤害同种嗅觉线索的反掠食性警觉性增强。

IF 2.3 2区 生物学 Q2 ECOLOGY
Resona Simkhada, Jhaman Kundun, Svetla Sofkova-Bobcheva, Xiong Zhao He
{"title":"猎物对受伤易受伤害同种嗅觉线索的反掠食性警觉性增强。","authors":"Resona Simkhada,&nbsp;Jhaman Kundun,&nbsp;Svetla Sofkova-Bobcheva,&nbsp;Xiong Zhao He","doi":"10.1002/ece3.72257","DOIUrl":null,"url":null,"abstract":"<p>Predation risk is a key evolutionary force shaping prey behaviors and life-history strategies across taxa. Predators often target vulnerable life stages of prey, but how prey females adjust their reproductive strategies in response to cues from injured conspecifics of these stages remains unclear, particularly in haplodiploid species, where mothers can adjust offspring sex ratios in response to social environments. Using the predatory mite <i>Phytoseiulus persimilis</i> and its prey, the spider mite <i>Tetranychus ludeni</i>, we first investigated the stage-specific vulnerability by exposing <i>T. ludeni</i> eggs, deutonymphs, and female adults to <i>P. persimilis</i> for choice. We then tested whether ovipositing <i>T. ludeni</i> females adjusted reproductive performances and survival when exposed to potential predatory cues from those injured conspecifics. Results show that <i>P. persimilis</i> significantly preferred <i>T. ludeni</i> eggs for feeding, indicating their higher vulnerability to predators. <i>T. ludeni</i> females responded most strongly to potential predatory cues from injured eggs, reducing fecundity and producing smaller eggs, but without trading off their longevity. Additionally, when exposed to injured adult cues, <i>T. ludeni</i> females adjusted offspring sex ratios, producing more dispersing daughters by fertilizing more smaller eggs, an evolved strategy to escape from the risky environments. In contrast, egg hatching and immature survival were unaffected by conspecific cues. Our results demonstrate that <i>T. ludeni</i> females may discriminate among cues from injured conspecifics of different life stages, with the strongest vigilance elicited by cues from the most vulnerable stage (i.e., eggs). This study highlights the role of indirect, life stage-specific cues in shaping antipredator strategies and reveals that non-consumptive effects of predation risk could influence prey population dynamics in ways beyond direct predation. Our findings provide a mechanistic understanding of reproductive plasticity in haplodiploid systems, offering new insights into how prey balance current and future reproductive investments under predation pressure.</p>","PeriodicalId":11467,"journal":{"name":"Ecology and Evolution","volume":"15 10","pages":""},"PeriodicalIF":2.3000,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12498088/pdf/","citationCount":"0","resultStr":"{\"title\":\"Stronger Antipredatory Vigilance of Prey to Olfactory Cues From Injured Vulnerable Conspecifics\",\"authors\":\"Resona Simkhada,&nbsp;Jhaman Kundun,&nbsp;Svetla Sofkova-Bobcheva,&nbsp;Xiong Zhao He\",\"doi\":\"10.1002/ece3.72257\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Predation risk is a key evolutionary force shaping prey behaviors and life-history strategies across taxa. Predators often target vulnerable life stages of prey, but how prey females adjust their reproductive strategies in response to cues from injured conspecifics of these stages remains unclear, particularly in haplodiploid species, where mothers can adjust offspring sex ratios in response to social environments. Using the predatory mite <i>Phytoseiulus persimilis</i> and its prey, the spider mite <i>Tetranychus ludeni</i>, we first investigated the stage-specific vulnerability by exposing <i>T. ludeni</i> eggs, deutonymphs, and female adults to <i>P. persimilis</i> for choice. We then tested whether ovipositing <i>T. ludeni</i> females adjusted reproductive performances and survival when exposed to potential predatory cues from those injured conspecifics. Results show that <i>P. persimilis</i> significantly preferred <i>T. ludeni</i> eggs for feeding, indicating their higher vulnerability to predators. <i>T. ludeni</i> females responded most strongly to potential predatory cues from injured eggs, reducing fecundity and producing smaller eggs, but without trading off their longevity. Additionally, when exposed to injured adult cues, <i>T. ludeni</i> females adjusted offspring sex ratios, producing more dispersing daughters by fertilizing more smaller eggs, an evolved strategy to escape from the risky environments. In contrast, egg hatching and immature survival were unaffected by conspecific cues. Our results demonstrate that <i>T. ludeni</i> females may discriminate among cues from injured conspecifics of different life stages, with the strongest vigilance elicited by cues from the most vulnerable stage (i.e., eggs). This study highlights the role of indirect, life stage-specific cues in shaping antipredator strategies and reveals that non-consumptive effects of predation risk could influence prey population dynamics in ways beyond direct predation. Our findings provide a mechanistic understanding of reproductive plasticity in haplodiploid systems, offering new insights into how prey balance current and future reproductive investments under predation pressure.</p>\",\"PeriodicalId\":11467,\"journal\":{\"name\":\"Ecology and Evolution\",\"volume\":\"15 10\",\"pages\":\"\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2025-10-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12498088/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Ecology and Evolution\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/ece3.72257\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ECOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ecology and Evolution","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/ece3.72257","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ECOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

捕食风险是影响整个类群猎物行为和生活史策略的关键进化力量。捕食者通常以脆弱的生命阶段为目标,但雌性猎物如何根据这些阶段受伤的同种动物的线索调整其生殖策略尚不清楚,特别是在单倍体物种中,母亲可以根据社会环境调整后代的性别比例。本研究以persimilis植物绥螨(Phytoseiulus persimilis)及其猎物ludanychus叶螨(Tetranychus ludeni)为研究对象,通过将ludeni卵、双鳞螨和雌成虫暴露于persimilis进行选择,研究了其阶段性脆弱性。然后,我们测试了产卵的雌T. ludeni在暴露于那些受伤的同种动物的潜在掠食性线索时是否会调整生殖表现和生存。结果表明,紫花假单胞虫明显倾向于进食卢德尼卵,表明其对捕食者的脆弱性较高。T. ludeni雌性对受伤卵的潜在捕食线索反应最强烈,减少繁殖力并产生较小的卵,但不会牺牲它们的寿命。此外,当接触到受伤的成年线索时,T. ludeni雌性会调整后代的性别比例,通过使更小的卵子受精来产生更多分散的女儿,这是一种逃离危险环境的进化策略。相比之下,卵的孵化和未成熟的存活不受同种线索的影响。研究结果表明,鲁德尼瓢虫雌性对来自不同生命阶段的受伤同种虫的提示具有明显的区别,其中来自最脆弱阶段(即卵)的提示引起的警觉性最强。这项研究强调了间接的、生命阶段特定的线索在形成反捕食者策略中的作用,并揭示了捕食风险的非消耗效应可能以直接捕食之外的方式影响猎物种群动态。我们的发现提供了对单倍体系统生殖可塑性的机制理解,为猎物在捕食压力下如何平衡当前和未来的生殖投资提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Stronger Antipredatory Vigilance of Prey to Olfactory Cues From Injured Vulnerable Conspecifics

Stronger Antipredatory Vigilance of Prey to Olfactory Cues From Injured Vulnerable Conspecifics

Predation risk is a key evolutionary force shaping prey behaviors and life-history strategies across taxa. Predators often target vulnerable life stages of prey, but how prey females adjust their reproductive strategies in response to cues from injured conspecifics of these stages remains unclear, particularly in haplodiploid species, where mothers can adjust offspring sex ratios in response to social environments. Using the predatory mite Phytoseiulus persimilis and its prey, the spider mite Tetranychus ludeni, we first investigated the stage-specific vulnerability by exposing T. ludeni eggs, deutonymphs, and female adults to P. persimilis for choice. We then tested whether ovipositing T. ludeni females adjusted reproductive performances and survival when exposed to potential predatory cues from those injured conspecifics. Results show that P. persimilis significantly preferred T. ludeni eggs for feeding, indicating their higher vulnerability to predators. T. ludeni females responded most strongly to potential predatory cues from injured eggs, reducing fecundity and producing smaller eggs, but without trading off their longevity. Additionally, when exposed to injured adult cues, T. ludeni females adjusted offspring sex ratios, producing more dispersing daughters by fertilizing more smaller eggs, an evolved strategy to escape from the risky environments. In contrast, egg hatching and immature survival were unaffected by conspecific cues. Our results demonstrate that T. ludeni females may discriminate among cues from injured conspecifics of different life stages, with the strongest vigilance elicited by cues from the most vulnerable stage (i.e., eggs). This study highlights the role of indirect, life stage-specific cues in shaping antipredator strategies and reveals that non-consumptive effects of predation risk could influence prey population dynamics in ways beyond direct predation. Our findings provide a mechanistic understanding of reproductive plasticity in haplodiploid systems, offering new insights into how prey balance current and future reproductive investments under predation pressure.

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
CiteScore
4.40
自引率
3.80%
发文量
1027
审稿时长
3-6 weeks
期刊介绍: Ecology and Evolution is the peer reviewed journal for rapid dissemination of research in all areas of ecology, evolution and conservation science. The journal gives priority to quality research reports, theoretical or empirical, that develop our understanding of organisms and their diversity, interactions between them, and the natural environment. Ecology and Evolution gives prompt and equal consideration to papers reporting theoretical, experimental, applied and descriptive work in terrestrial and aquatic environments. The journal will consider submissions across taxa in areas including but not limited to micro and macro ecological and evolutionary processes, characteristics of and interactions between individuals, populations, communities and the environment, physiological responses to environmental change, population genetics and phylogenetics, relatedness and kin selection, life histories, systematics and taxonomy, conservation genetics, extinction, speciation, adaption, behaviour, biodiversity, species abundance, macroecology, population and ecosystem dynamics, and conservation policy.
×
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