Metabolic allometric scaling of multicellular organisms as a product of evolutionary development and optimization of food chains

TL;DR

This paper proposes that metabolic allometric scaling across species results from natural selection optimizing energy distribution within food chains, ensuring stability and sufficient resources for reproduction.

Contribution

It introduces a biomechanical model linking locomotion and energy expenditure to allometric scaling, explaining its evolutionary origin and quantitative predictions.

Findings

Calculated allometric exponents closely match experimental data for mammals.

Model supports that energy distribution optimization underpins metabolic scaling.

Highlights evolutionary pressures shaping resource allocation in food chains.

Abstract

Production of energy is a foundation of life. Metabolic rate of organisms (amount of energy produced per unit time) generally increases slower than organisms' mass, which has important implications for life organization. This phenomenon, when considered across different taxa, is called interspecific allometric scaling. Its origin has puzzled scientists for many decades, and still is considered unknown. In this paper we posit that natural selection, as determined by evolutionary pressures, leads to distribution of resources, and accordingly energy, within a food chain, which is optimal from the perspective of stability of the food chain, when each species has sufficient amount of resources for continuous reproduction, but not too much to jeopardize existence of other species. Metabolic allometric scaling is then a quantitative representation of this optimal distribution. Taking locomotion and the primary mechanism for distribution of energy, we developed a biomechanical model to find energy expenditures, considering limb length, skeleton mass and speed. Using the interspecific allometric exponents for these three measures and substituting into the locomotion-derived model for energy expenditure, we calculated allometric exponents for mammals, reptiles, fish and birds, and compared these values with allometric exponents derived from experimental observations. The calculated allometric exponents were nearly identical to experimentally observed exponents for mammals, and very close for fish, reptiles and the basal metabolic rate of birds. The main result of the study is that the metabolic allometric scaling is a function of a mechanism of optimal energy distribution between the species of a food chain. This optimized sharing of common resources provides stability of a food chain for a given habitat and is guided by evolutionary pressures and natural selection.