{"title":"在回声定位蝙蝠中,呼叫产生和翅拍耦合是灵活的和物种特异性的","authors":"Hangjing Xia, Nina Ma, Aoqiang Li, Jinhong Luo","doi":"10.1111/nyas.15325","DOIUrl":null,"url":null,"abstract":"Echolocation and flight are two key behavioral innovations that contribute to the evolutionary success and diversification of bats, which are classified phylogenetically into two suborders: Yinpterochiroptera and Yangochiroptera. Considerable research has identified a coupling between call production and wingbeat in flying bats, although only a few have quantified the relationship and all were restricted to bats from the suborder Yangochiroptera. Here, we quantitatively compared the coupling between call production and wingbeat in two representative species of bats, <i>Hipposideros pratti</i> of the suborder Yinpterochiroptera and <i>Myotis pilosus</i> of the suborder Yangochiroptera, under identical experimental settings. We found that (1) both species exhibited the temporal coupling of call production and wingbeat; (2) the degree of coupling is species-specific, with <i>M. pilosus</i> showing a tighter coupling between call timing and wingbeat cycle than <i>H. pratti</i>; (3) the coupling is a plastic trait, as evidenced by the effect of environmental clutter in <i>H. pratti</i>; and (4) there is no evidence that the coupling of call production and wingbeat limits the source level control in either species. We suggest that the coupling between call production and wingbeat is flexible and species-specific, which may not compromise precise echolocation control in bats.","PeriodicalId":8250,"journal":{"name":"Annals of the New York Academy of Sciences","volume":"58 1","pages":""},"PeriodicalIF":4.1000,"publicationDate":"2025-03-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Call production and wingbeat coupling is flexible and species-specific in echolocating bats\",\"authors\":\"Hangjing Xia, Nina Ma, Aoqiang Li, Jinhong Luo\",\"doi\":\"10.1111/nyas.15325\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Echolocation and flight are two key behavioral innovations that contribute to the evolutionary success and diversification of bats, which are classified phylogenetically into two suborders: Yinpterochiroptera and Yangochiroptera. Considerable research has identified a coupling between call production and wingbeat in flying bats, although only a few have quantified the relationship and all were restricted to bats from the suborder Yangochiroptera. Here, we quantitatively compared the coupling between call production and wingbeat in two representative species of bats, <i>Hipposideros pratti</i> of the suborder Yinpterochiroptera and <i>Myotis pilosus</i> of the suborder Yangochiroptera, under identical experimental settings. We found that (1) both species exhibited the temporal coupling of call production and wingbeat; (2) the degree of coupling is species-specific, with <i>M. pilosus</i> showing a tighter coupling between call timing and wingbeat cycle than <i>H. pratti</i>; (3) the coupling is a plastic trait, as evidenced by the effect of environmental clutter in <i>H. pratti</i>; and (4) there is no evidence that the coupling of call production and wingbeat limits the source level control in either species. We suggest that the coupling between call production and wingbeat is flexible and species-specific, which may not compromise precise echolocation control in bats.\",\"PeriodicalId\":8250,\"journal\":{\"name\":\"Annals of the New York Academy of Sciences\",\"volume\":\"58 1\",\"pages\":\"\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2025-03-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Annals of the New York Academy of Sciences\",\"FirstCategoryId\":\"103\",\"ListUrlMain\":\"https://doi.org/10.1111/nyas.15325\",\"RegionNum\":3,\"RegionCategory\":\"综合性期刊\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of the New York Academy of Sciences","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1111/nyas.15325","RegionNum":3,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
Call production and wingbeat coupling is flexible and species-specific in echolocating bats
Echolocation and flight are two key behavioral innovations that contribute to the evolutionary success and diversification of bats, which are classified phylogenetically into two suborders: Yinpterochiroptera and Yangochiroptera. Considerable research has identified a coupling between call production and wingbeat in flying bats, although only a few have quantified the relationship and all were restricted to bats from the suborder Yangochiroptera. Here, we quantitatively compared the coupling between call production and wingbeat in two representative species of bats, Hipposideros pratti of the suborder Yinpterochiroptera and Myotis pilosus of the suborder Yangochiroptera, under identical experimental settings. We found that (1) both species exhibited the temporal coupling of call production and wingbeat; (2) the degree of coupling is species-specific, with M. pilosus showing a tighter coupling between call timing and wingbeat cycle than H. pratti; (3) the coupling is a plastic trait, as evidenced by the effect of environmental clutter in H. pratti; and (4) there is no evidence that the coupling of call production and wingbeat limits the source level control in either species. We suggest that the coupling between call production and wingbeat is flexible and species-specific, which may not compromise precise echolocation control in bats.
期刊介绍:
Published on behalf of the New York Academy of Sciences, Annals of the New York Academy of Sciences provides multidisciplinary perspectives on research of current scientific interest with far-reaching implications for the wider scientific community and society at large. Each special issue assembles the best thinking of key contributors to a field of investigation at a time when emerging developments offer the promise of new insight. Individually themed, Annals special issues stimulate new ways to think about science by providing a neutral forum for discourse—within and across many institutions and fields.