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Sleep is an evolutionarily ancient behavior, yet multiple cave-dwelling populations of the Mexican tetra, Astyanax mexicanus, have converged on sleep loss compared to surface fish. However, most of the 34 cave populations remain unstudied, and sleep in natural habitats is largely unknown. To address this, we measured sleep and activity in 15 representative populations of surface, cave, and hybrid populations. All cavefish and hybrid populations tested exhibited drastically reduced sleep, including hybrid populations with diverse eye and pigmentation phenotypes. Mapping behavior onto the A. mexicanus phylogeny revealed that reduced sleep and elevated locomotor activity evolved independently multiple times. Field experiments confirmed that wild fish also exhibit sleep loss, paralleling laboratory findings. These results demonstrate deep evolutionary convergence on sleep loss across cavefish lineages and suggest that sleep reduction is a primary trait contributing to adaptation in subterranean environments. 

Abstract Laboratory studies have demonstrated that a single phenotype can be produced by many different genotypes; however, in natural systems, it is frequently found that phenotypic convergence is due to parallel genetic changes. This suggests a substantial role for constraint and determinism in evolution and indicates that certain mutations are more likely to contribute to phenotypic evolution. Here we use whole genome resequencing in the Mexican tetra,Astyanax mexicanus, to investigate how selection has shaped the repeated evolution of both trait loss and enhancement across independent cavefish lineages. We show that selection on standing genetic variation and de novo mutations both contribute substantially to repeated adaptation. Our findings provide empirical support for the hypothesis that genes with larger mutational targets are more likely to be the substrate of repeated evolution and indicate that features of the cave environment may impact the rate at which mutations occur.