Understanding mechanisms of avian flight by integrating observations with tests of competing hypotheses.

IF 2.6 2区 生物学 Q2 BIOLOGY Journal of Experimental Biology Pub Date : 2025-02-15 Epub Date: 2025-02-20 DOI:10.1242/jeb.247992
Douglas L Altshuler, Vikram B Baliga, Anthony B Lapsansky, Phillip Lee, Eric R Press, Jolan S Theriault
{"title":"Understanding mechanisms of avian flight by integrating observations with tests of competing hypotheses.","authors":"Douglas L Altshuler, Vikram B Baliga, Anthony B Lapsansky, Phillip Lee, Eric R Press, Jolan S Theriault","doi":"10.1242/jeb.247992","DOIUrl":null,"url":null,"abstract":"<p><p>A long-standing problem in the study of avian flight is determining how biomechanics and physiology are associated with behaviour, ecological interactions and evolution. In some avian clades, flight mechanisms are strongly linked to ecology. Hummingbirds, for example, exhibit traits that support both hovering flight and nectar foraging. In most avian clades, however, features such as wing shape are highly variable among taxa without clear relationships to biomechanics, energetics or ecology. In this Commentary, we discuss challenges to understanding associations between phenotype and performance in avian flight. A potential pitfall in studies that attempt to link trait specialization with performance is that the most relevant traits and environments are not being considered. Additionally, a large number of studies of the mechanisms of avian flight are highly phenomenological. Although observations are essential for hypothesis development, we argue that for our discipline to make progress, we will need much more integration of the observational phase with developing crucial tests of competing hypotheses. Direct comparison of alternative hypotheses can be accomplished through analytical frameworks as well as through experimentation.</p>","PeriodicalId":15786,"journal":{"name":"Journal of Experimental Biology","volume":"228 Suppl_1","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2025-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Experimental Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1242/jeb.247992","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/20 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

A long-standing problem in the study of avian flight is determining how biomechanics and physiology are associated with behaviour, ecological interactions and evolution. In some avian clades, flight mechanisms are strongly linked to ecology. Hummingbirds, for example, exhibit traits that support both hovering flight and nectar foraging. In most avian clades, however, features such as wing shape are highly variable among taxa without clear relationships to biomechanics, energetics or ecology. In this Commentary, we discuss challenges to understanding associations between phenotype and performance in avian flight. A potential pitfall in studies that attempt to link trait specialization with performance is that the most relevant traits and environments are not being considered. Additionally, a large number of studies of the mechanisms of avian flight are highly phenomenological. Although observations are essential for hypothesis development, we argue that for our discipline to make progress, we will need much more integration of the observational phase with developing crucial tests of competing hypotheses. Direct comparison of alternative hypotheses can be accomplished through analytical frameworks as well as through experimentation.

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
通过整合观察和相互竞争的假设的测试来理解鸟类飞行的机制。
鸟类飞行研究中的一个长期问题是确定生物力学和生理学如何与行为、生态相互作用和进化相关联。在一些鸟类进化分支中,飞行机制与生态密切相关。例如,蜂鸟表现出既支持悬停飞行又支持采蜜的特征。然而,在大多数鸟类分支中,翼形等特征在不同的分类群之间变化很大,与生物力学、能量学或生态学没有明确的关系。在这篇评论中,我们讨论了理解鸟类飞行中表型和性能之间关系的挑战。在试图将特质专业化与表现联系起来的研究中,一个潜在的陷阱是,最相关的特质和环境没有被考虑在内。此外,大量关于鸟类飞行机制的研究都是高度现象学的。虽然观察对于假设的发展是必不可少的,但我们认为,为了使我们的学科取得进展,我们将需要更多地将观察阶段与开发竞争性假设的关键测试结合起来。对不同假设的直接比较可以通过分析框架和实验来完成。
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
CiteScore
5.50
自引率
10.70%
发文量
494
审稿时长
1 months
期刊介绍: Journal of Experimental Biology is the leading primary research journal in comparative physiology and publishes papers on the form and function of living organisms at all levels of biological organisation, from the molecular and subcellular to the integrated whole animal.
期刊最新文献
An ancient oxidase lost in vertebrates promotes extreme stress tolerance in an emerging Cnidarian model for ecology, evolution, and biomedicine. Antho-RFamide effect on light production in the bioluminescent sea pen Pennatula phosphorea (Octocorallia, Pennatulacea). Oxygen availability and oxygen delivery, but not oxidative stress shape heat tolerance in diploid and triploid zebrafish larvae. Halocline boundary layer restricts the vertical distribution of the box jellyfish Tripedalia cystophora. Extinction, spontaneous recovery, and ABA renewal in the cricket Gryllus bimaculatus.
×
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学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
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