Velocity as an overlooked driver in the echolocation behavior of aerial hawking vespertilionid bats.

IF 8.1 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Lasse Jakobsen, Danuta M Wisniewska, Felix T Häfele, Josephine T Rajaeasparan, Julie B Nielsen, John M Ratcliffe
{"title":"Velocity as an overlooked driver in the echolocation behavior of aerial hawking vespertilionid bats.","authors":"Lasse Jakobsen, Danuta M Wisniewska, Felix T Häfele, Josephine T Rajaeasparan, Julie B Nielsen, John M Ratcliffe","doi":"10.1016/j.cub.2024.12.042","DOIUrl":null,"url":null,"abstract":"<p><p>Moving animals must gather information at sufficient rates, detail, and range relative to their velocity while filtering this information to that essential for a given task.<sup>1</sup><sup>,</sup><sup>2</sup> Echolocators, because of their active sensory system, are exceptional models for investigating how animals filter and adjust information flow to motor patterns.<sup>3</sup><sup>,</sup><sup>4</sup> During airborne prey capture, bats adjust echolocation and, by extension, how they probe for information in distance- and context-dependent ways.<sup>5</sup><sup>,</sup><sup>6</sup><sup>,</sup><sup>7</sup> We investigated how sensory probing guides movement and how niche specializations shape strategies to integrate information acquisition and motion velocity. Specifically, we recorded three sympatric bats of the same foraging guild (edge-space hawkers), but different niches, as they intercepted airborne prey under identical conditions. When hawking, we find that the trawler, Myotis daubentonii, and the hawker, Pipistrellus pygmaeus, exhibit similar flight and echolocation behavior, whereas the gleaner, M. nattereri, flies slower and produces calls of lower duration and intensity, greater bandwidth and call interval, but similar beam breadth. Strikingly, these differences in echolocation behavior converge when accounting for flight speed. We show that these species move equivalent distances between call emissions and that all bats travel through their respective sonar ranges in the same time interval. Further, each echolocation call's duration is related to the two-way travel time of its sonar range, and thus velocity, the same way across species. The similarity in how these bats sample their environment relative to velocity suggests general mechanisms of information processing and conserved traits underlying auditory attention in vespertilionid bats and, perhaps, other echolocators.</p>","PeriodicalId":11359,"journal":{"name":"Current Biology","volume":" ","pages":""},"PeriodicalIF":8.1000,"publicationDate":"2025-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.cub.2024.12.042","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Moving animals must gather information at sufficient rates, detail, and range relative to their velocity while filtering this information to that essential for a given task.1,2 Echolocators, because of their active sensory system, are exceptional models for investigating how animals filter and adjust information flow to motor patterns.3,4 During airborne prey capture, bats adjust echolocation and, by extension, how they probe for information in distance- and context-dependent ways.5,6,7 We investigated how sensory probing guides movement and how niche specializations shape strategies to integrate information acquisition and motion velocity. Specifically, we recorded three sympatric bats of the same foraging guild (edge-space hawkers), but different niches, as they intercepted airborne prey under identical conditions. When hawking, we find that the trawler, Myotis daubentonii, and the hawker, Pipistrellus pygmaeus, exhibit similar flight and echolocation behavior, whereas the gleaner, M. nattereri, flies slower and produces calls of lower duration and intensity, greater bandwidth and call interval, but similar beam breadth. Strikingly, these differences in echolocation behavior converge when accounting for flight speed. We show that these species move equivalent distances between call emissions and that all bats travel through their respective sonar ranges in the same time interval. Further, each echolocation call's duration is related to the two-way travel time of its sonar range, and thus velocity, the same way across species. The similarity in how these bats sample their environment relative to velocity suggests general mechanisms of information processing and conserved traits underlying auditory attention in vespertilionid bats and, perhaps, other echolocators.

求助全文
约1分钟内获得全文 求助全文
来源期刊
Current Biology
Current Biology 生物-生化与分子生物学
CiteScore
11.80
自引率
2.20%
发文量
869
审稿时长
46 days
期刊介绍: Current Biology is a comprehensive journal that showcases original research in various disciplines of biology. It provides a platform for scientists to disseminate their groundbreaking findings and promotes interdisciplinary communication. The journal publishes articles of general interest, encompassing diverse fields of biology. Moreover, it offers accessible editorial pieces that are specifically designed to enlighten non-specialist readers.
×
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:481959085
Book学术官方微信