Clade-Specific Allometries in Avian Basal Metabolic Rate Demand a Broader Theory of Allometry.

IF 1.8 3区 生物学 Q3 PHYSIOLOGY Physiological and Biochemical Zoology Pub Date : 2023-05-01 DOI:10.1086/725207
Samantha M Giancarli, Arthur E Dunham, Michael P O'Connor
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引用次数: 3

Abstract

AbstractMany attempts at providing a single-scale exponent and mechanism to explain metabolic rate assert a monolithic selective mechanism for allometries, characterized by a universal allometric scale power (usually chosen to be 0.75). To test for the deviations from universal allometric scaling, we gathered data from previously published metabolic measurements on 903 bird species and performed regressions of log(basal metabolic rate) and log(body mass) for (1) all birds and (2) 20 monophyletic clades within birds. We constructed two Bayesian linear mixed models-one included ecological variables and the other included data for mammals from Sieg et al. (2009). Overall allometric patterns differed significantly among clades of birds, and some clades were not consistent with the 0.75 scale power. We were unable to find apparent physiological, morphological, phylogenetic, or ecological characteristics among clades, predicting a difference in allometry or consistency with any previously proposed universal allometry. The Bayesian analysis illuminated novel bivariate, clade-specific differences in scaling slope-intercept space, separating large groups of birds and mammals. While significantly related to basal metabolic rate, feeding guild and migratory tendency had small effects compared to clade and body mass. We propose that allometric hypotheses, in general, must extend beyond simple overarching mechanisms to allow for conflicting and interacting influences that produce allometric patterns at narrower taxonomic scales-perhaps including other processes whose optimization may interfere with that of the system proposed by the metabolic theory of ecology.

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鸟类基础代谢率的进化支特异性异速反应需要更广泛的异速反应理论。
摘要许多提供单一尺度指数和机制来解释代谢率的尝试都主张异速反应的单一选择机制,其特征是通用的异速反应尺度功率(通常选择0.75)。为了检验普遍异速测量的偏差,我们收集了先前发表的903种鸟类的代谢测量数据,并对(1)所有鸟类和(2)鸟类内20个单系进化枝的log(基础代谢率)和log(体重)进行了回归。我们构建了两个贝叶斯线性混合模型——一个包含生态变量,另一个包含Sieg et al.(2009)的哺乳动物数据。整体异速生长模式在不同枝系间存在显著差异,部分枝系与0.75尺度功率不一致。我们无法在进化支中发现明显的生理、形态、系统发育或生态特征,无法预测异速生长的差异或与任何先前提出的普遍异速生长的一致性。贝叶斯分析揭示了新的双变量,进化枝特异性差异的尺度斜截空间,分离大群的鸟类和哺乳动物。摄食行当和迁徙倾向与基础代谢率有显著相关性,但与支系和体重相比影响较小。我们提出异速假说,一般来说,必须超越简单的总体机制,以允许在更窄的分类尺度上产生异速模式的冲突和相互作用的影响-可能包括其他过程,其优化可能会干扰生态学代谢理论提出的系统。
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来源期刊
CiteScore
3.20
自引率
6.20%
发文量
62
审稿时长
6-12 weeks
期刊介绍: Physiological and Biochemical Zoology: Ecological and Evolutionary Approaches primarily publishes original research in animal physiology and biochemistry as considered from behavioral, ecological, and/or evolutionary perspectives. Studies at all levels of biological organization from the molecular to the whole organism are welcome, and work that integrates across levels of organization is particularly encouraged. Studies that focus on behavior or morphology are welcome, so long as they include ties to physiology or biochemistry, in addition to having an ecological or evolutionary context. Subdisciplines of interest include nutrition and digestion, salt and water balance, epithelial and membrane transport, gas exchange and transport, acid-base balance, temperature adaptation, energetics, structure and function of macromolecules, chemical coordination and signal transduction, nitrogen metabolism and excretion, locomotion and muscle function, biomechanics, circulation, behavioral, comparative and mechanistic endocrinology, sensory physiology, neural coordination, and ecotoxicology ecoimmunology.
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