The occurrence of anomalous coloration (albinism, leucism and melanism) in mammals is a rare phenomenon in nature, but this phenomenon has been reported for several species of mammals. In this study, we report on the occurrence of leucism in Eira barbara by examining three road-killed individuals and two sightings of live animals in Reserva Particular do Patrimônio Natural Santuário do Caraça, southeastern Brazil. In addition, we examined tayra specimens housed in mammal collections from Brazil and USA. The animals found dead and those sighted had a whitish yellow fur on the body and head, resulting in lighter coloration than the coloring pattern commonly observed in tayras. Despite these lighter color pattern, the specimens showed parts of soft tissue, such as iris and the skin, with pigmentation very similar to that present in individuals with the typical color pattern. This set of factors indicates the specimens recorded were in fact leucistic and not albino. Among the specimens examined in the scientific collections, we found nine individuals from different localities that presented the whitish yellow color pattern. Some studies attribute the higher frequency of cases of leucism due to small populations and / or with some mechanism of reproductive isolation. Thus, analysis of the genetic variability of populations containing individuals with such characteristics should be considered. On the other hand, the occurrence of polymorphic color phenotype in tayras indicates that hypotheses related to the fixation of recessive characteristics, or on possible environmental adaptive advantages of these phenotypes can be tested.

The association of immobility and camouflage is widespread as a defensive mechanism in prey from varied taxa. However, many experiments assessing the reaction of prey to predator cues are conducted under artificial laboratory conditions. In a previous experiment we observed the tadpoles of Ololygon machadoi (Hylidae) to respond to predator visual and/or chemical cues by choosing backgrounds that improve their disruptive properties, but detected no associated reduction of movement. Here we experimentally demonstrate this response in the species' natural habitat, on backgrounds where the tadpoles are likely to achieve their best camouflage. We also tested whether previous experiences could influence both background choice and immobility in O. machadoi tadpoles. these novel experimental results suggest that a defensive behavior-i.e., reduction of movement-in these tadpoles is more strongly expressed under the natural conditions where they evolved, compared to laboratory conditions where prey and predator were brought into closer contact. Besides, previous experiences are likely to play an important role in expressed defensive responses. Prey species are under constant selection to escape predation. They can develop predator specific responses, but some responses seem to be widespread, such as spatial avoidance of predators and reduction of activity 1. In this context prey species that count on camouflage to reduce the probability of being detected by predators tend to remain motionless, aiding to the protective properties of their colouration 2,3. Reduction of movement is likely to reduce detection probability and can emerge as a spontaneous response when the detected threat is at a distance (background threat), but an approaching (immediate) threat may otherwise elicit an escape response 4. Previous experience can also determine the reaction of prey to specific predators 5 , however there is evidence that evolutionary pressures may have led prey species to develop different defensive mechanisms and express each one in appropriate contexts determined by the assessed threat 4. Both innate and learned defensive behaviours can be expressed even in very early life stages 6,7. Tadpoles, the larvae of biphasic anuran amphibians, are frequently employed in experiments conducted to study the reaction of prey to predator cues 8 , due to their broad range of predators and defensive mechanisms 1. It has been shown that many species of tadpoles reduce movement in the presence of predators 1,9. However, these studies are usually conducted under laboratory or mesocosm conditions, sometimes within reduced spaces in artificial standardized containers where predator cues are manipulated, other factors kept equal, to record tadpole reaction to particular cues 1,10. Under such circumstances, both visual and chemical stimuli have been

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