Painful venoms are used to deter predators. Pain itself, however, can signal damage and thus serves an important adaptive function. Evolution to reduce general pain responses, although valuable for preying on venomous species, is rare, likely because it comes with the risk of reduced response to tissue damage. Bark scorpions capitalize on the protective pain pathway of predators by inflicting intensely painful stings. However, grasshopper mice regularly attack and consume bark scorpions, grooming only briefly when stung. Bark scorpion venom induces pain in many mammals (house mice, rats, humans) by activating the voltage-gated Na+ channel Nav1.7, but has no effect on Nav1.8. Grasshopper mice Nav1.8 has amino acid variants that bind bark scorpion toxins and inhibit Na+ currents, blocking action potential propagation and inducing analgesia. Thus, grasshopper mice have solved the predator-pain problem by using a toxin bound to a nontarget channel to block transmission of the pain signals the venom itself is initiating.

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Traditional general education science courses appear ineffective at helping students improve their critical-thinking skills and engage with discomforting topics (e.g., evolution). A novel course focusing on the nature of science rather than the findings of science significantly overcame both deficiencies.

Sexual dimorphism can result from sexual or ecological selective pressures, but the importance of alternative reproductive roles and trait compensation in generating phenotypic differences between the sexes is poorly understood. We evaluated morphological and behavioral sexual dimorphism in striped bark scorpions (Centruroides vittatus). We propose that reproductive roles have driven sexually dimorphic body mass in this species which produces sex differences in locomotor performance. Poor locomotor performance in the females (due to the burden of being gravid) favors compensatory aggression as part of an alternative defensive strategy, while male morphology is coadapted to support a sprinting-based defensive strategy. We tested the effects of sex and morphology on stinging and sprinting performance and characterized overall differences between the sexes in aggressiveness towards simulated threats. Greater body mass was associated with higher sting rates and slower sprinting within sexes, which explained the greater aggression of females (the heavier sex) and, along with longer legs in males, the improved sprint performance in males. These findings suggest females are aggressive to compensate for locomotor costs of reproduction while males possess longer legs to enhance sprinting for predator evasion and mate finding. Sexual dimorphism in the metasoma (“tail”) was unrelated to stinging and sprinting performance and may best be explained by sexual selection.

Burrowing owls nest and roost in ground squirrel burrows, a refuge frequently used by rattlesnakes. When cornered, burrowing owls produce a vocal hiss that has been suggested to mimic a rattlesnake's rattle. To test this hypothesis, we conducted an experiment using two populations of Douglas ground squirrels that differ in their evolutionary histories with rattlesnakes. Both squirrel populations were sympatric with burrowing owls. Squirrels from a population subjected to natural selection by rattlesnakes treated the owl hiss as cautiously as they did the rattle, and responded with greater caution to the rattle and hiss than to two control sounds. Squirrels from a rattlesnake‐free area, however, were less systematic in differentiating among the rattle, the hiss, and the control treatments. Such variation between ground‐squirrel populations provides evidence that the burrowing owl's defensive hiss currently functions as an acoustic Batesian mimic of a rattlesnake's rattle.