Why does the growth of most life forms exhibit a narrow range of optimal temperatures below 40°C? We hypothesize that the recently identified stable range of oceanic temperatures of ~5 to 37°C for more than two billion years of Earth history tightly constrained the evolution of prokaryotic thermal performance curves to optimal temperatures for growth to less than 40°C. We tested whether competitive mechanisms reproduced the observed upper limits of life's temperature optima using simple Lotka–Volterra models of interspecific competition between organisms with different temperature optima. Model results supported our proposition whereby organisms with temperature optima up to 37°C were most competitive. Model results were highly robust to a wide range of reasonable variations in temperature response curves of modeled species. We further propose that inheritance of prokaryotic genes and subsequent co‐evolution with microbial partners may have resulted in eukaryotes also fixing their temperature optima within this narrow temperature range. We hope this hypothesis will motivate considerable discussion and future work to advance our understanding of the remarkable consistency of the temperature dependence of life.
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