{"title":"Diet-Induced Developmental and Morphological Plasticity in a Thelytokous Predatory Mite Amblyseius herbicolus (Chant) (Acari: Phytoseiidae)","authors":"Keshi Zhang, Zhi-Qiang Zhang","doi":"10.1002/ece3.72280","DOIUrl":null,"url":null,"abstract":"<p>Phenotypic plasticity enables organisms to adjust developmental and morphological responses to environmental variations, including prey availability. In this study, we investigated how variation in prey consumption influences immature development and adult morphometric traits in the predatory mite <i>Amblyseius herbicolus</i> (Chant). Using two laboratory-reared populations originating from Auckland and Tauranga, New Zealand, we assessed the relationship between prey consumption and immature development and morphological outcomes. While differences in prey consumption did not significantly alter developmental duration, individuals with higher prey consumption attained a larger size at maturity. Several morphometric traits, including r3 length, primary metapodal plate length, Leg III, and Leg IV, were also significantly influenced by diet, indicating that plasticity extends beyond developmental traits to morphological characteristics in <i>A. herbicolus</i>. Population origin also accounted for some variations in developmental and morphometric traits, although it remains unclear whether these differences arose from genetic divergence or prolonged rearing under controlled conditions. This study underscores the importance of actual prey consumption rates—rather than prey availability or density—in shaping morphological variations. It also suggests diet-induced plasticity may affect phytoseiid mite taxonomy.</p>","PeriodicalId":11467,"journal":{"name":"Ecology and Evolution","volume":"15 10","pages":""},"PeriodicalIF":2.3000,"publicationDate":"2025-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12516015/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ecology and Evolution","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/ece3.72280","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
Abstract
Phenotypic plasticity enables organisms to adjust developmental and morphological responses to environmental variations, including prey availability. In this study, we investigated how variation in prey consumption influences immature development and adult morphometric traits in the predatory mite Amblyseius herbicolus (Chant). Using two laboratory-reared populations originating from Auckland and Tauranga, New Zealand, we assessed the relationship between prey consumption and immature development and morphological outcomes. While differences in prey consumption did not significantly alter developmental duration, individuals with higher prey consumption attained a larger size at maturity. Several morphometric traits, including r3 length, primary metapodal plate length, Leg III, and Leg IV, were also significantly influenced by diet, indicating that plasticity extends beyond developmental traits to morphological characteristics in A. herbicolus. Population origin also accounted for some variations in developmental and morphometric traits, although it remains unclear whether these differences arose from genetic divergence or prolonged rearing under controlled conditions. This study underscores the importance of actual prey consumption rates—rather than prey availability or density—in shaping morphological variations. It also suggests diet-induced plasticity may affect phytoseiid mite taxonomy.
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.