Illness, death, and costs of immunity and injury strongly select for avoidance of predators or contagion. Ants, cockroaches, and collembola recognize their dead using unsaturated fatty acids (e.g., oleic or linoleic acid) as ''necromone'' cues. Ants, bees, and termites remove dead from their nests (necrophoric behavior) whereas semisocial species seal off corpses or simply avoid their dead or injured (necrophobic behavior). Alarm and avoidance responses to exudates from injured conspecifics are widespread. This involves diverse pheromones, complex chemistry and learning. We hypothesized that necromones are a phylogenetically ancient class of related signals and predicted that terrestrial Isopoda (that strongly aggregate and lack known dispersants) would avoid body fluids and corpses using fatty acid ''necromones.'' Isopods were repelled by crushed conspecifics (blood), intact corpses, and alcohol extracts of bodies. As predicted, the repellent fraction contained oleic and linoleic acids and authentic standards repelled several isopod species. We further predicted a priori that social caterpillars (lacking known dispersants) would be repelled by their own body fluids and unsaturated fatty acids. Both tent caterpillars and fall webworms avoided branches treated with conspecific body fluid. Oleic and linoleic acids were also strongly avoided by both species. Necromone signaling appears widespread and likely traces to aquatic ancestors pre-dating the divergence of the Crustacea and Hexapoda at least 420 million years ago.

Which factor determines animal aggressivity? Wynn-Edwards proposed the hypothesis that aggressive level increases with population density; Adams and Mesterton-Gibbons proposed the hypothesis that body weight is an indicator of animal aggressivity; however, Smith and Price hypothesized that aggression level varied with external conditions; that is, the population lived in the most unfavorable environment demonstrated the highest average aggression level, and the population that lived under the most favorable external conditions demonstrated the lowest average aggression level. In this paper, we tested these three hypotheses by manipulating enclosed root vole (Microtus oeconomus) populations under different food and predation treatments and observed their aggressive behavior. Aggressive behavior was measured by matching mice in a neutral arena. The experimental results supported Smith and Price's hypothesis and Adams and Mesterton-Gibbons's hypothesis; however, they did not support WynnEdwards' hypothesis. Moreover, we found that reproductively active individuals were more aggressive. We concluded that the growth of population density did not cause or otherwise bring about increased aggressive behavior of root voles, but the external factors (predation and food supply) and physical factors (body weight and reproductive condition) were significantly correlated with aggression levels in a root vole population.