Variations in ambient light conditions across different microhabitats can modify the detectability of predators and prey. Prey have been shown to be more visible in sunlit than in shaded patches, leading to higher predation risk and more investment in vigilance (predation risk hypothesis). Additionally, prey have been hypothesized to take longer to detect predators in sunlit compared to shaded patches because of the excess of sunlight causing glare effects (disability glare hypothesis). We tested the predictions of these two non‐mutually exclusive hypotheses in a seminatural experiment with brown‐headed cowbirds by measuring vigilance behavior and detection of a ground predator in patches under the shade of vegetation and in the open. Light intensity and achromatic contrast were higher in the sunlit patches, which could enhance glare effects, but chromatic contrast was higher in the shaded patches. Brown‐headed cowbirds took longer to show alert reactions to and flee from a ground predator in sunlit compared to shaded patches. However, the two parameters associated with perceived predation risk (vigilance prior to the predator exposure and time to resume foraging after the attack) did not differ between sunlit and shaded patches. Our findings support to a greater extent the disability glare hypothesis than the predation risk hypothesis. Overall, ambient light conditions can affect two critical components of behavioral predator–prey interactions in terrestrial habitats: detection of and escape from predators. The effects of disability glare are expected to be more pronounced in bird species with wider visual fields or without sun‐shading structures; however, species may compensate through various behaviors (e.g. avoidance of sunlit patches and changes in head orientation).
SUMMARYColor vision is not uniform across the retina because of differences in photoreceptor density and distribution. Retinal areas with a high density of cone photoreceptors may overlap with those with a high density of ganglion cells, increasing hue discrimination. However, there are some exceptions to this cell distribution pattern, particularly in species with horizontal visual streaks (bands of high ganglion cell density across the retina) that live in open habitats. We studied the spectral sensitivity and distribution of cone photoreceptors involved in chromatic and achromatic vision in the Canada goose (Branta canadiensis), which possesses an oblique rather than horizontal visual streak at the ganglion cell layer. Using microspectrophotometry, we found that the Canada goose has a violet-sensitive visual system with four visual pigments with absorbance peaks at 409, 458, 509 and 580nm. The density of most cones involved in chromatic and achromatic vision peaked along a band across the retina that matched the oblique orientation of the visual streak. With the information on visual sensitivity, we calculated chromatic and achromatic contrasts of different goose plumage regions. The regions with the highest visual saliency (cheek, crown, neck and upper tail coverts) were the ones involved in visual displays to maintain flock cohesion. The Canada goose oblique visual streak is the retinal center for chromatic and achromatic vision, allowing individuals to sample the sky and the ground simultaneously or the horizon depending on head position. Overall, our results show that the Canada goose visual system has features that make it rather different from that of other vertebrates living in open habitats.
Animals generally live in multisensory worlds; however, our understanding of multisensory perception is rather limited, despite its relevance for explaining the mechanisms behind social interactions, such as collective detection while foraging in groups. We tested how multisensory stimuli affected the antipredator behavior of dark‐eyed juncos (Junco hyemalis) using alarm calls as an auditory signal and flushing behavior as a visual cue. We varied the degree of risk within the group by manipulating the number of group mates alarm calling and/or flushing using robotic birds. We assumed that alarm calling and flushing were redundant stimuli and predicted that they could generate one of three types of responses (enhancement, equivalence, or antagonism) depending on the mechanism of multisensory perception. We set up an artificial flock with three robotic juncos surrounding a live junco and controlled for multiple confounding factors (e.g., identity of the focal, body mass, food deprivation time). We found that the degree of alarm of live juncos increased when at least one robot flushed. However, the time it took the live individuals to react to the robots' behavior increased, rather than decreased, with at least one alarm call. This could be the result of an orienting response or sensory overload, as live juncos increased scanning behavior after being exposed solely to alarm calls. Contrary to some theoretical assumptions, alarm calling and flushing behavior elicited independent unimodal responses, suggesting that they are non‐redundant stimuli and that together they could reduce the occurrence of false alarms and facilitate flock cohesion.
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