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For example, individuals use their body coloration to avoid detection and recognition, startle predators, signal unpalatability, and divert predator attacks ([4]). [3] review provides a novel and refreshing perspective on the conflicting selection pressures that shape animal coloration, and the multifunctional strategies that have evolved as a result. Thus, the categorization of defensive coloration strategies provides a unique opportunity to re-examine the link between coloration and behavioral defense in the context of function(s) and mechanism(s). [Extracted from the article]

The effects of intrasexual and intersexual selection on male trait evolution can be difficult to disentangle, especially based on observational data. Male-male competition can limit an observer's ability to identify the effect of female mate choice independently from sexual coercion. Here, we use an experimental approach to explore whether an ornament, the red facial skin exhibited by male rhesus macaques (Macaca mulatta), might be involved in both female mate choice and male-male competition. We used a noninvasive experimental approach based on the looking time paradigm in a free-ranging setting, showing images of differently colored male faces to both adult females (N= 91) and males (N= 77), as well as to juveniles (N= 94) as a control. Results show that both adult females and males looked longer at dark red faces compared with pale pink ones. However, when considering the proportion of subjects that looked longer at dark red faces regardless of preference strength, only females showed a significant dark red bias. In contrast, juveniles did not show any preferences between stimuli, suggesting that the adult bias is not a consequence of the experimental design or related to a general sensory bias for red coloration among all age-sex classes. Collectively, these results support the role the ornament plays in female mate choice in this species and provide the first evidence that this ornament may play a role in male-male competition as well, despite a general lack of observational evidence for the latter effect to date. [ABSTRACT FROM AUTHOR]

Why are some snakes blotchy and others stripy? Evidence suggests it mainly depends on a snake’s behavior strategy. Analysis of the patterns of 171 species of North American and Australian snakes showed that blotched snakes are generally large ambush hunters, whereas plain and striped snakes are especially active or flee rapidly away from predator.Species in the suborder Serpentes present a powerful model for understanding processes involved in visual signal design. Although vision is generally poor in snakes, they are often both predators and prey of visually oriented species. We examined how ecological and behavioral factors have driven the evolution of snake patterning using a phylogenetic comparative approach. The appearances of 171 species of Australian and North American snakes were classified using a reaction-diffusion model of pattern development, the parameters of which allow parametric quantification of various aspects of coloration. The main findings include associations between plain color and an active hunting strategy, longitudinal stripes and rapid escape speed, blotched patterns with ambush hunting, slow movement and pungent cloacal defense, and spotted patterns with close proximity to cover. Expected associations between bright colors, aggressive behavior, and venom potency were not observed. The mechanisms through which plain and longitudinally striped patterns might support camouflage during movement are discussed. The flicker-fusion hypothesis for transverse striped patterns being perceived as uniform color during movement is evaluated as theoretically possible but unlikely. Snake pattern evolution is generally phylogenetically conservative, but by sampling densely in a wide variety of snake lineages, we have demonstrated that similar pattern phenotypes have evolved repeatedly in response to similar ecological demands. [ABSTRACT FROM AUTHOR]

Sexual selection produces extravagant male traits, such as colorful ornaments, via female mate choice. More rarely, in mating systems in which males allocate mating effort between multiple females, female ornaments may evolve via male mate choice. Females of many anthropoid primates exhibit ornaments that indicate intraindividual cyclical fertility, but which have also been proposed to function as interindividual quality signals. Rhesus macaque females are one such species, exhibiting cyclical facial color variation that indicates ovulatory status, but in which the function of interindividual variation is unknown. We collected digital images of the faces of 32 rhesus macaque adult females. We assessed mating rates, and consortship by males, according to female face coloration. We also assessed whether female coloration was linked to physical (skinfold fat, body mass index) or physiological (fecal glucocorticoid metabolite [fGCM], urinary C-peptide concentrations) condition. We found that redder-faced females were mated more frequently, and consorted for longer periods by top-ranked males. Redder females had higher fGCM concentrations, perhaps related to their increased mating activity and consequent energy mobilization, and blood flow. Prior analyses have shown that female facial redness is a heritable trait, and that redder-faced females have higher annual fecundity, while other evidence suggests that color expression is likely to be a signal rather than a cue. Collectively, the available evidence suggests that female coloration has evolved at least in part via male mate choice. Its evolution as a sexually selected ornament attractive to males is probably attributable to the high female reproductive synchrony found in this species. [ABSTRACT FROM AUTHOR]