• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

对于蛙类叫声而言,异速生长以逃脱声学限制的情况十分罕见。

Allometric escape from acoustic constraints is rare for frog calls.

作者信息

Tonini João Filipe Riva, Provete Diogo B, Maciel Natan M, Morais Alessandro Ribeiro, Goutte Sandra, Toledo Luís Felipe, Pyron Robert Alexander

机构信息

Department of Biological Sciences The George Washington University Washington DC USA.

Museum of Comparative Zoology Department of Organismic and Evolutionary Biology Harvard University Cambridge MA USA.

出版信息

Ecol Evol. 2020 Mar 7;10(8):3686-3695. doi: 10.1002/ece3.6155. eCollection 2020 Apr.

DOI:10.1002/ece3.6155
PMID:32313627
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7160179/
Abstract

Allometric constraint is a product of natural selection and physical laws, particularly with respect to body size and traits constrained by properties thereof, such as metabolism, longevity, and vocal frequency. Allometric relationships are often conserved across lineages, indicating that physical constraints dictate scaling patterns in deep time, despite substantial genetic and ecological divergence among organisms. In particular, acoustic allometry (sound frequency ~ body size) is conserved across frogs, in defiance of massive variation in both body size and frequency. Here, we ask how many instances of allometric escape have occurred across the frog tree of life using a Bayesian framework that estimates the location, number, and magnitude of shifts in the adaptive landscape of acoustic allometry. Moreover, we test whether ecology in terms of calling site could affect these relationships. We find that calling site has a major influence on acoustic allometry. Despite this, we identify only four major instances of allometric escape, potentially deriving from ecomorphological adaptations to new signal modalities. In these instances of allometric escape, the optima and strength of the scaling relationship are different than expected for most other frog species, representing new adaptive regimes of body size ~ call frequency. Allometric constraints on frog calls are highly conserved and have rarely allowed escape, despite frequent invasions of new adaptive regimes and dramatic ecomorphological divergence. Our results highlight the rare instances in which natural and sexual selection combined can overcome physical constraints on sound production.

摘要

异速生长约束是自然选择和物理定律的产物,特别是关于身体大小以及受其属性(如新陈代谢、寿命和发声频率)约束的性状。异速生长关系通常在不同谱系中得以保留,这表明尽管生物体之间存在显著的遗传和生态差异,但物理约束在漫长的时间里决定了缩放模式。特别是,声学异速生长(声音频率身体大小)在青蛙中是保守的,尽管身体大小和频率都存在巨大差异。在这里,我们使用贝叶斯框架来估计声学异速生长适应性景观中变化的位置、数量和幅度,以此探究在青蛙生命之树上发生了多少例异速生长逃逸的情况。此外,我们测试了鸣叫地点的生态因素是否会影响这些关系。我们发现鸣叫地点对声学异速生长有重大影响。尽管如此,我们仅识别出四个主要的异速生长逃逸实例,可能源于对新信号模式的生态形态适应。在这些异速生长逃逸的实例中,缩放关系的最优值和强度与大多数其他青蛙物种的预期不同,代表了身体大小鸣叫频率的新适应模式。尽管新的适应模式频繁出现且生态形态差异巨大,但青蛙叫声的异速生长约束高度保守,很少出现逃逸情况。我们的研究结果突出了自然选择和性选择相结合能够克服声音产生的物理约束的罕见实例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9769/7160179/348243786c72/ECE3-10-3686-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9769/7160179/ef49e4268dc0/ECE3-10-3686-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9769/7160179/393881b99236/ECE3-10-3686-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9769/7160179/348243786c72/ECE3-10-3686-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9769/7160179/ef49e4268dc0/ECE3-10-3686-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9769/7160179/393881b99236/ECE3-10-3686-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9769/7160179/348243786c72/ECE3-10-3686-g003.jpg

相似文献

1
Allometric escape from acoustic constraints is rare for frog calls.对于蛙类叫声而言,异速生长以逃脱声学限制的情况十分罕见。
Ecol Evol. 2020 Mar 7;10(8):3686-3695. doi: 10.1002/ece3.6155. eCollection 2020 Apr.
2
Hidden shifts in allometry scaling between sound production and perception in anurans.在两栖动物中,声音产生和感知之间的异速生长比例关系存在隐藏的变化。
PeerJ. 2023 Nov 3;11:e16322. doi: 10.7717/peerj.16322. eCollection 2023.
3
Allometric conservatism in the evolution of bird beaks.鸟类喙进化中的异速生长保守性。
Evol Lett. 2021 Dec 27;6(1):83-91. doi: 10.1002/evl3.267. eCollection 2022 Feb.
4
Allometric constraints and the evolution of allometry.生长律制约与生长律进化。
Evolution. 2014 Mar;68(3):866-85. doi: 10.1111/evo.12312. Epub 2013 Dec 19.
5
Neotropical frogs and mating songs: The evolution of advertisement calls in glassfrogs.新热带蛙类和交配歌曲:玻璃蛙求爱叫声的进化。
J Evol Biol. 2019 Feb;32(2):163-176. doi: 10.1111/jeb.13406. Epub 2018 Dec 18.
6
Environmental and phylogenetic aspects affect in different ways the acoustic niche of a frog community in southeastern Brazil.环境和进化方面以不同的方式影响巴西东南部一个蛙类群落的声学生态位。
An Acad Bras Cienc. 2022 Jan 7;94(1):e20200705. doi: 10.1590/0001-3765202220200705. eCollection 2022.
7
Environmental and morphological constraints interact to drive the evolution of communication signals in frogs.环境和形态学限制因素相互作用,推动了青蛙通讯信号的进化。
J Evol Biol. 2020 Dec;33(12):1749-1757. doi: 10.1111/jeb.13713. Epub 2020 Oct 18.
8
Evolutionary and Allometric Insights into Anuran Auditory Sensitivity and Morphology.对有尾两栖动物听觉敏感性和形态的进化和比例分析的见解。
Brain Behav Evol. 2022;97(3-4):140-150. doi: 10.1159/000521309. Epub 2021 Dec 3.
9
Individual variation in two types of advertisement calls of Pacific tree frogs, , and the implications for sexual selection and species recognition.太平洋树蛙两种广告叫声的个体差异及其对性选择和物种识别的影响。
Bioacoustics. 2021;30(4):437-457. doi: 10.1080/09524622.2020.1803133. Epub 2020 Aug 12.
10
Ontogenetic drivers of morphological evolution in monitor lizards and allies (Squamata: Paleoanguimorpha), a clade with extreme body size disparity.亲缘分支法分析探讨巨蜥及其近缘物种(有鳞目:古蜥蜴亚目)中极度体型差异的形态演化的个体发生驱动因素
BMC Ecol Evol. 2022 Feb 12;22(1):15. doi: 10.1186/s12862-022-01970-6.

引用本文的文献

1
Call variation and calling site preference of three sympatric frogs.三种同域分布蛙类的鸣声变异及鸣声位点偏好
Curr Zool. 2024 Nov 28;71(4):492-503. doi: 10.1093/cz/zoae067. eCollection 2025 Aug.
2
Evolution of sexual size dimorphism in tetrapods is driven by varying patterns of sex-specific selection on size.四足动物两性异形的进化是由对体型的性别特异性选择的不同模式驱动的。
Nat Ecol Evol. 2025 Mar;9(3):464-473. doi: 10.1038/s41559-024-02600-8. Epub 2024 Dec 23.
3
Allometric Constraint Predominates Over the Acoustic Adaptation Hypothesis in a Radiation of Neotropical Treefrogs.

本文引用的文献

1
Neotropical frogs and mating songs: The evolution of advertisement calls in glassfrogs.新热带蛙类和交配歌曲:玻璃蛙求爱叫声的进化。
J Evol Biol. 2019 Feb;32(2):163-176. doi: 10.1111/jeb.13406. Epub 2018 Dec 18.
2
Phylogenetic Comparative Analysis: A Modeling Approach for Adaptive Evolution.系统发育比较分析:一种适应性进化的建模方法。
Am Nat. 2004 Dec;164(6):683-695. doi: 10.1086/426002.
3
Functional biogeography of angiosperms: life at the extremes.被子植物的功能生物地理学:极限生活。
在新热带树蛙辐射中,异速生长限制比声学适应假说更为重要。
Integr Zool. 2025 Jul;20(4):763-773. doi: 10.1111/1749-4877.12920. Epub 2024 Dec 10.
4
Hidden shifts in allometry scaling between sound production and perception in anurans.在两栖动物中,声音产生和感知之间的异速生长比例关系存在隐藏的变化。
PeerJ. 2023 Nov 3;11:e16322. doi: 10.7717/peerj.16322. eCollection 2023.
5
Convergent Anuran Middle Ear Loss Lacks a Universal, Adaptive Explanation.趋同的蛙类中耳损失缺乏普遍的、适应性的解释。
Brain Behav Evol. 2023;98(6):290-301. doi: 10.1159/000534936. Epub 2023 Nov 1.
6
Critical calls: Circadian and seasonal periodicity in vocal activity in a breeding colony of Panamanian golden frogs (Atelopus zeteki).关键电话:巴拿马金蛙(Atelopus zeteki)繁殖群中发声活动的昼夜和季节性周期性。
PLoS One. 2023 Aug 17;18(8):e0286582. doi: 10.1371/journal.pone.0286582. eCollection 2023.
7
Signal size allometry in lizard dewlaps.蜥蜴“喉扇”的信号大小比例关系。
Biol Lett. 2023 Jul;19(7):20230160. doi: 10.1098/rsbl.2023.0160. Epub 2023 Jul 5.
8
Using citizen science to test for acoustic niche partitioning in frogs.利用公民科学测试青蛙的声学生态位分区。
Sci Rep. 2022 Feb 14;12(1):2447. doi: 10.1038/s41598-022-06396-0.
9
Geographic variation in the matching between call characteristics and tympanic sensitivity in the Weeping lizard.哀痛蜥叫声特征与鼓膜敏感性匹配的地理变异
Ecol Evol. 2021 Dec 14;11(24):18633-18650. doi: 10.1002/ece3.8469. eCollection 2021 Dec.
10
Description and evolution of the larynx of the Physalaemus olfersii species group, with remarks on the laryngeal anatomy of the P. cuvieri clade (Amphibia: Anura: Leiuperinae).Physalaemus olfersii 物种组的喉描述和演化,以及对 P. cuvieri 进化枝(两栖动物:无尾目:细趾蟾科)的喉解剖结构的讨论。
J Anat. 2021 Sep;239(3):557-582. doi: 10.1111/joa.13436. Epub 2021 Apr 4.
New Phytol. 2018 Jun;218(4):1697-1709. doi: 10.1111/nph.15114. Epub 2018 Mar 30.
4
The interplay of past diversification and evolutionary isolation with present imperilment across the amphibian tree of life.过去的多样化和进化隔离与当前的生存威胁在两栖动物生命之树上的相互作用。
Nat Ecol Evol. 2018 May;2(5):850-858. doi: 10.1038/s41559-018-0515-5. Epub 2018 Mar 26.
5
Acoustic allometry revisited: morphological determinants of fundamental frequency in primate vocal production.重新审视声学异速生长:灵长类动物发声中基频的形态学决定因素
Sci Rep. 2017 Sep 5;7(1):10450. doi: 10.1038/s41598-017-11000-x.
6
The Evolution of Energetic Scaling across the Vertebrate Tree of Life.脊椎动物生命之树中能量标度的演化
Am Nat. 2017 Aug;190(2):185-199. doi: 10.1086/692326. Epub 2017 May 31.
7
The use of bioacoustics in anuran taxonomy: theory, terminology, methods and recommendations for best practice.生物声学在无尾两栖类分类学中的应用:理论、术语、方法及最佳实践建议。
Zootaxa. 2017 Apr 11;4251(1):1-124. doi: 10.11646/zootaxa.4251.1.1.
8
Genetic diversity of Morato's Digger Toad, Proceratophrys moratoi: spatial structure, gene flow, effective size and the need for differential management strategies of populations.莫拉托掘足蟾(Proceratophrys moratoi)的遗传多样性:空间结构、基因流、有效种群大小以及种群差异化管理策略的必要性
Genet Mol Biol. 2017 Apr-Jun;40(2):502-514. doi: 10.1590/1678-4685-gmb-2016-0025. Epub 2017 Jun 5.
9
THE ORIGIN AND FUNCTION OF "BIZARRE" STRUCTURES: ANTLER SIZE AND SKULL SIZE IN THE "IRISH ELK," MEGALOCEROS GIGANTEUS.“怪异”结构的起源与功能:巨型爱尔兰麋鹿(大角鹿)的鹿角大小与头骨大小
Evolution. 1974 Jun;28(2):191-220. doi: 10.1111/j.1558-5646.1974.tb00740.x.
10
Do Macrophylogenies Yield Stable Macroevolutionary Inferences? An Example from Squamate Reptiles.宏观系统发育能得出稳定的宏观进化推论吗?以有鳞目爬行动物为例。
Syst Biol. 2017 Sep 1;66(5):843-856. doi: 10.1093/sysbio/syw102.