Harrison Jon F, Biewener Andrew, Bernhardt Joanna R, Burger Joseph R, Brown James H, Coto Zach N, Duell Meghan E, Lynch Michael, Moffett Emma R, Norin Tommy, Pettersen Amanda K, Smith Felisa A, Somjee Ummat, Traniello James F A, Williams Terrie M
School of Life Sciences, Arizona State University, Tempe, AZ, USA.
Harvard University Department of Organismic & Evolutionary Biology, Cambridge, MA, USA.
Integr Comp Biol. 2022 Aug 6;62(5):1395-418. doi: 10.1093/icb/icac136.
Larger animals studied during ontogeny, across populations, or across species, usually have lower mass-specific metabolic rates than smaller animals (hypometric scaling). This pattern is usually observed regardless of physiological state (e.g. basal, resting, field, maximally-active). The scaling of metabolism is usually highly correlated with the scaling of many life history traits, behaviors, physiological variables, and cellular/molecular properties, making determination of the causation of this pattern challenging. For across-species comparisons of resting and locomoting animals (but less so for across populations or during ontogeny), the mechanisms at the physiological and cellular level are becoming clear. Lower mass-specific metabolic rates of larger species at rest are due to a) lower contents of expensive tissues (brains, liver, kidneys), and b) slower ion leak across membranes at least partially due to membrane composition, with lower ion pump ATPase activities. Lower mass-specific costs of larger species during locomotion are due to lower costs for lower-frequency muscle activity, with slower myosin and Ca++ ATPase activities, and likely more elastic energy storage. The evolutionary explanation(s) for hypometric scaling remain(s) highly controversial. One subset of evolutionary hypotheses relies on constraints on larger animals due to changes in geometry with size; for example, lower surface-to-volume ratios of exchange surfaces may constrain nutrient or heat exchange, or lower cross-sectional areas of muscles and tendons relative to body mass ratios would make larger animals more fragile without compensation. Another subset of hypotheses suggests that hypometric scaling arises from biotic interactions and correlated selection, with larger animals experiencing less selection for mass-specific growth or neurolocomotor performance. A additional third type of explanation comes from population genetics. Larger animals with their lower effective population sizes and subsequent less effective selection relative to drift may have more deleterious mutations, reducing maximal performance and metabolic rates. Resolving the evolutionary explanation for the hypometric scaling of metabolism and associated variables is a major challenge for organismal and evolutionary biology. To aid progress, we identify some variation in terminology use that has impeded cross-field conversations on scaling. We also suggest that promising directions for the field to move forward include: 1) studies examining the linkages between ontogenetic, population-level, and cross-species allometries, 2) studies linking scaling to ecological or phylogenetic context, 3) studies that consider multiple, possibly interacting hypotheses, and 4) obtaining better field data for metabolic rates and the life history correlates of metabolic rate such as lifespan, growth rate and reproduction.
在个体发育过程中、跨种群或跨物种研究的较大动物,通常比小型动物具有更低的质量特异性代谢率(降比缩放)。无论生理状态如何(例如基础、静息、野外、最大活动状态),通常都能观察到这种模式。代谢的缩放通常与许多生活史特征、行为、生理变量以及细胞/分子特性的缩放高度相关,这使得确定这种模式的因果关系具有挑战性。对于静息和运动动物的跨物种比较(但跨种群或个体发育过程中的比较则较少),生理和细胞水平的机制正变得清晰。较大物种静息时较低的质量特异性代谢率归因于:a)昂贵组织(大脑、肝脏、肾脏)的含量较低,以及b)至少部分由于膜组成导致的跨膜离子泄漏较慢,离子泵ATP酶活性较低。较大物种运动时较低的质量特异性成本归因于较低频率肌肉活动的成本较低,肌球蛋白和Ca++ATP酶活性较慢,并且可能有更多的弹性能量储存。降比缩放的进化解释仍然极具争议。进化假说的一个子集依赖于由于几何形状随尺寸变化而对较大动物的限制;例如,交换表面较低的表面积与体积比可能会限制营养物质或热量交换,或者相对于体重比而言,肌肉和肌腱较低的横截面积会使较大动物在没有补偿的情况下更加脆弱。另一个子集的假说表明,降比缩放源于生物相互作用和相关选择,较大动物在质量特异性生长或神经运动性能方面受到的选择较少。另外第三种解释来自群体遗传学。有效种群规模较低且相对于漂变而言后续选择效率较低的较大动物可能有更多有害突变,从而降低最大性能和代谢率。解决代谢及相关变量降比缩放的进化解释是有机体生物学和进化生物学面临的一项重大挑战。为推动进展,我们识别了一些阻碍跨领域关于缩放问题交流的术语使用差异。我们还建议该领域向前发展的有前景方向包括:1)研究个体发育、种群水平和跨物种异速生长之间的联系,2)将缩放与生态或系统发育背景联系起来的研究,3)考虑多个可能相互作用假说的研究,以及4)获取关于代谢率以及代谢率与寿命、生长率和繁殖等生活史相关性的更好的野外数据。