Abstract
BackgroundResource allocation trade-off between storage and somatic growth is an essential physiological phenomenon in animals. Revealing its patterns and underlying mechanisms are fundamental for behavior, evolutionary, and population ecological studies. Currently, our understanding of the real-time resource allocating patterns in animals is still limited, and the underlying metabolic mechanisms have been rarely investigated. The life strategy of amphibian larvae relies on precise coordination between storage and somatic growth, which makes them good model for studying this issue.ResultsHere, the resource allocation strategy was investigated for Rana omeimontis tadpoles, who exhibit prominent hepatic fat-accumulation. Results showed that their ontogenetic fat accumulation emerged when tadpoles grew to a body weight range of 30–50 mg, where their fat storage had a high priority in resource allocation. Beyond this range, the resource proportion for somatic growth increased, but continuous storage investment was likely maintained to kept higher body fat index in larger individuals. This seeming paradoxical allocation pattern could be explained by assuming a positive relationship between storage abundance and the investment to somatic growth. This speculation was supported by the observation that storage had the priority in resource allocation to reach a higher body fat index before increment in body weight when food level increased. Moreover, it was also supported by the metabolic pattern that presented lipid-based energy metabolism after ontogenetic fat accumulation, and activating the mobilization of fat storage in the liver can promote the somatic growth. In short, fat synthesis and fat accumulation in the liver may well modulated the resource allocation to somatic growth, and their liver likes a reservoir with valves to regulate energy flow for the downstream developmental processes.ConclusionIn Rana omeimontis tadpoles, their hepatic fat level positively modulated the resource allocation to somatic growth through lipid-based energy metabolism. We reveal the real-time resource allocation pattern in an amphibian tadpole and explain it at molecular level. These results likely provide a new mechanistic insight into the resource allocation in animals.