The effects of parasitism on sex allocation of a hermaphroditic acorn barnacle.

IF 2.1 3区 生物学 Q3 ECOLOGY Journal of Evolutionary Biology Pub Date : 2025-02-27 DOI:10.1093/jeb/voaf007
Masami M Tamechika, Hiroyuki Yamada, Shigeho Ijiri, Yoichi Yusa
{"title":"The effects of parasitism on sex allocation of a hermaphroditic acorn barnacle.","authors":"Masami M Tamechika, Hiroyuki Yamada, Shigeho Ijiri, Yoichi Yusa","doi":"10.1093/jeb/voaf007","DOIUrl":null,"url":null,"abstract":"<p><p>Sex allocation theory predicts the adaptive allocation of resources to male versus female reproduction in simultaneous hermaphrodites in response to individual characteristics or environmental factors. Because parasites uptake resources from their hosts, their presence could affect the sex allocation of the hosts. We investigated the effects of infestation status and infestation intensity by the rhizocephalan barnacle Boschmaella japonica on reproduction, including sex allocation, of the host intertidal barnacle Chthamalus challengeri. Feeding activity was also examined as a factor related to resource intake. Both male and female reproductive investment decreased with increasing parasite infestation, and the sex allocation of large-infested hosts was more male-biased than that of large uninfested hosts. Moreover, in contrast to the model prediction that male investment does not change under resource limitation, male investment decreased in infested hosts whose resources were taken by parasites. This reduction in male investment could be explained by changes in mating group size, since infested hosts have shorter penises and consequently are able to access fewer mating partners.</p>","PeriodicalId":50198,"journal":{"name":"Journal of Evolutionary Biology","volume":" ","pages":"417-429"},"PeriodicalIF":2.1000,"publicationDate":"2025-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Evolutionary Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/jeb/voaf007","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ECOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Sex allocation theory predicts the adaptive allocation of resources to male versus female reproduction in simultaneous hermaphrodites in response to individual characteristics or environmental factors. Because parasites uptake resources from their hosts, their presence could affect the sex allocation of the hosts. We investigated the effects of infestation status and infestation intensity by the rhizocephalan barnacle Boschmaella japonica on reproduction, including sex allocation, of the host intertidal barnacle Chthamalus challengeri. Feeding activity was also examined as a factor related to resource intake. Both male and female reproductive investment decreased with increasing parasite infestation, and the sex allocation of large-infested hosts was more male-biased than that of large uninfested hosts. Moreover, in contrast to the model prediction that male investment does not change under resource limitation, male investment decreased in infested hosts whose resources were taken by parasites. This reduction in male investment could be explained by changes in mating group size, since infested hosts have shorter penises and consequently are able to access fewer mating partners.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
性别分配理论预测,同时雌雄同体的动物会根据个体特征或环境因素对雄性繁殖和雌性繁殖的资源进行适应性分配。由于寄生虫从宿主那里摄取资源,它们的存在可能会影响宿主的性别分配。我们研究了根瘤蚤藤壶对宿主潮间带藤壶(Chthamalus challengeri)繁殖(包括性别分配)的侵扰状态和侵扰强度的影响。此外,还研究了与资源摄取有关的摄食活动。随着寄生虫感染率的增加,雄性和雌性的生殖投资都减少了,而且感染寄生虫的大型寄主的性别分配比未感染寄生虫的大型寄主更偏向于雄性。此外,与模型预测的雄性投资在资源限制条件下不会发生变化相反,在资源被寄生虫侵占的寄主中,雄性投资减少了。雄性投资减少的原因可能是交配群体规模的变化,因为受侵染的宿主阴茎较短,因此能够获得的交配对象较少。
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 去求助
来源期刊
Journal of Evolutionary Biology
Journal of Evolutionary Biology 生物-进化生物学
CiteScore
4.20
自引率
4.80%
发文量
152
审稿时长
3-6 weeks
期刊介绍: It covers both micro- and macro-evolution of all types of organisms. The aim of the Journal is to integrate perspectives across molecular and microbial evolution, behaviour, genetics, ecology, life histories, development, palaeontology, systematics and morphology.
期刊最新文献
Adaptation for crypsis versus conspicuous social signalling following transitions across an extreme ecotone. High altitude favours long-chained cuticular hydrocarbons in Drosophila. Like mother, like daughter? Phenotypic plasticity, environmental covariation, and heritability of size in a parthenogenetic wasp. Unexpected absence of a multiple-queen supergene haplotype from supercolonial populations of Formica ants. The coevolution of parasite virulence, and host investment in constitutive and induced defense.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1