We compared species mean data on the size of functionally distinct brain regions to test the relative rates at which investment in higher-order cognitive processing (mushroom body calyces) versus peripheral sensory processing (optic and antennal lobes) increased with increasing brain size. Subjects were eusocial paper wasps from queen and worker castes of 10 species from different genera. Relative investment in central processing tissue increased with brain size at a higher rate than peripheral structure investment, demonstrating that tissue devoted to higher-order cognitive processing is more constrained by brain size. This pattern held for raw data and for phylogenetically independent contrasts. These findings suggest that there is a minimum necessary investment in peripheral sensory processing brain tissue, with little to gain from additional investment. In contrast, increased brain size provides opportunities to invest in additional higher-order cognitive processing tissue. Reproductive castes differed within species in brain tissue investment, with higher central-to-peripheral brain tissue ratios in queens than in workers. Coupled with previous findings that paper wasp queen, but not worker, brain architecture corresponds to ecological and social variation, queen brain evolution appears to be most strongly shaped by cognitive demands, such as social interactions. These evolutionary patterns of neural investment echo findings in other animal lineages and have important implications, given that a greater investment in higherorder processing has been shown to increase the prevalence of complex and flexible behaviors across the animal kingdom.Hymenoptera | mushroom bodies | social brain | Vespidae A s brains evolve, both relative expansion of specific brain regions and general increases in absolute brain size can enable changes in animal cognitive capacity (1). Of particular note is the frequent convergent evolution of central brain regions that perform higher-order cognitive processing. Larger central processing centers are associated with enhanced capacity for learning, memory, and behavioral innovation among species (1-3). In primates, increased investment in higher-order cognitive processing structures, such as the neocortex and hippocampus, has been linked to increased cognitive performance (4), and the neocortex is five times larger in primates than in insectivores after accounting for differences in whole brain size (5). Increased hippocampal size in passerine birds has been associated with improved memory and the advent of food-storing behavior (6). Increased size and complexity of the mushroom bodies (MB), the neural centers of higher-order cognitive processing in insects, are paired with an increase in the prevalence of generalist feeding ecologies across species (7) and with social dominance status within species (8-10).Molecular evidence supports a single origin of the CNS in bilaterally symmetrical animals, including insects and vertebrates, occurring before the protostome-deuterostome split (11). ...