Alessandra Bartimachi, Thais B Pimenta, Francismeire J Telles, Ernane H M Vieira-Neto, João C F Cardoso, Heraldo L Vasconcelos, Alan N Costa
{"title":"Morphological divergence of domatia in ant-free populations of the widespread Neotropical myrmecophyte Miconia tococa (Melastomataceae)","authors":"Alessandra Bartimachi, Thais B Pimenta, Francismeire J Telles, Ernane H M Vieira-Neto, João C F Cardoso, Heraldo L Vasconcelos, Alan N Costa","doi":"10.1093/biolinnean/blae026","DOIUrl":null,"url":null,"abstract":"Co-evolving organisms experience multiple selection pressures that may lead to trait mismatches among different populations and sites. In defensive ant–plant mutualisms, host plants (myrmecophytes) produce specialized shelters (domatia) to harbour specialized ant-partners in exchange for protection against enemies. Although populations of myrmecophytes without ants occur in some locations, there are no records of changes in domatia morphology—at the population level—due to the absence of symbiotic ants. We conducted broad-scale samplings of Miconia tococa (Melastomataceae) populations across the Brazilian Cerrado and a 2-year transplant experiment to test whether domatia morphology changes when symbiotic ants are naturally absent. Domatia were 33.9% smaller in ant-free populations than in ant-inhabited populations. Transplants revealed that host plants from ant-inhabited sites still developed larger domatia than those from ant-free sites, even in the absence of ant-partners. These findings point to a change of M. tococa traits associated with biotic defences where symbiotic ants are absent. What may have begun as a plastic adjustment to ant-free environments appears to have been transformed into fixed (genetic) interpopulation differences over time, indicating a potential local destabilization of the mutualism or a mechanism to stabilize the interaction at the landscape scale.","PeriodicalId":55373,"journal":{"name":"Biological Journal of the Linnean Society","volume":"16 1","pages":""},"PeriodicalIF":2.0000,"publicationDate":"2024-03-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biological Journal of the Linnean Society","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/biolinnean/blae026","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"EVOLUTIONARY BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Co-evolving organisms experience multiple selection pressures that may lead to trait mismatches among different populations and sites. In defensive ant–plant mutualisms, host plants (myrmecophytes) produce specialized shelters (domatia) to harbour specialized ant-partners in exchange for protection against enemies. Although populations of myrmecophytes without ants occur in some locations, there are no records of changes in domatia morphology—at the population level—due to the absence of symbiotic ants. We conducted broad-scale samplings of Miconia tococa (Melastomataceae) populations across the Brazilian Cerrado and a 2-year transplant experiment to test whether domatia morphology changes when symbiotic ants are naturally absent. Domatia were 33.9% smaller in ant-free populations than in ant-inhabited populations. Transplants revealed that host plants from ant-inhabited sites still developed larger domatia than those from ant-free sites, even in the absence of ant-partners. These findings point to a change of M. tococa traits associated with biotic defences where symbiotic ants are absent. What may have begun as a plastic adjustment to ant-free environments appears to have been transformed into fixed (genetic) interpopulation differences over time, indicating a potential local destabilization of the mutualism or a mechanism to stabilize the interaction at the landscape scale.
期刊介绍:
The Biological Journal of the Linnean Society is a direct descendant of the oldest biological journal in the world, which published the epoch-making papers on evolution by Darwin and Wallace. The Journal specializes in evolution in the broadest sense and covers all taxonomic groups in all five kingdoms. It covers all the methods used to study evolution, whether whole-organism or molecular, practical or theoretical.d.