Impact of developmental temperature on neural growth, connectivity, and function

Environmental temperature dictates the developmental pace of poikilothermic animals. In Drosophila, slower development at lower temperatures results in higher brain connectivity, but the generality of such scaling across temperatures and brain regions and its impact on function are unclear. Here, we show that brain connectivity scales continuously across temperatures, in agreement with a first-principle model that postulates different metabolic constraints for the growth of the brain and the organism. The model predicts brain wiring under temperature cycles and the nonuniform temporal scaling of neural development across temperatures. Developmental temperature has notable effects on odor-driven behavior. Dissecting the circuit architecture and function of neurons in the olfactory pathway, we demonstrate that developmental temperature does not alter odor encoding in first- and second-order neurons, but it shifts the specificity of connections onto third-order neurons that mediate innate behaviors. We conclude that while some circuit computations are robust to the effects of developmental temperature on wiring, others exhibit phenotypic plasticity with possible adaptive advantages.