With their eyes on long vertical stalks, their panoramic visual field and their pronounced equatorial acute zone for vertical resolving power, the visual system of fiddler crabs is exquisitely tuned to the geometry of vision in the flat world of inter-tidal mudflats. The crabs live as burrow-centred grazers in dense, mixed-sex, mixed-age and mixed-species colonies, with the active space of an individual rarely exceeding 1 m(2). The full behavioural repertoire of fiddler crabs can thus be monitored over extended periods of time on a moment to moment basis together with the visual information they have available to guide their actions. These attributes make the crabs superb subjects for analysing visual tasks and the design of visual processing mechanisms under natural conditions, a prerequisite for understanding the evolution of visual systems. In this review we show, on the one hand, how deeply embedded fiddler crab vision is in the behavioural and the physical ecology of these animals and, on the other hand, how their behavioural options are constrained by their perceptual limitations. Studying vision in fiddler crabs reminds us that vision has a topography, that it is context-dependent and pragmatic and that there are perceptual limits to what animals can know and therefore care about.

Nesting insects perform learning flights to establish a visual representation of the nest environment that allows them to subsequently return to the nest. It has remained unclear when insects learn what during these flights, what determines their overall structure, and, in particular, how what is learned is used to guide an insect's return. We analyzed learning flights in ground-nesting wasps (Sphecidae: Cerceris australis) using synchronized high-speed cameras to determine 3D head position and orientation. Wasps move along arcs centered on the nest entrance, whereby rapid changes in gaze assure that the nest is seen at lateral positions in the left or the right visual field. Between saccades, the wasps translate along arc segments around the nest while keeping gaze fixed. We reconstructed panoramic views along the paths of learning and homing wasps to test specific predictions about what wasps learn during their learning flights and how they use this information to guide their return. Our evidence suggests that wasps monitor changing views during learning flights and use the differences they experience relative to previously encountered views to decide when to begin a new arc. Upon encountering learned views, homing wasps move left or right, depending on the nest direction associated with that view, and in addition appear to be guided by features on the ground close to the nest. We test our predictions on how wasps use views for homing by simulating homing flights of a virtual wasp guided by views rendered in a 3D model of a natural wasp environment.

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Mating signals are often directed at numerous senses and provide information about species identity, gender, receptiveness, individual identity and mate quality. Given the diversity of colourful body patterns in invertebrates, surprisingly few studies have examined the role of these visual signals in mate recognition. Here, we demonstrate the use of claw coloration as a species recognition signal in a fiddler crab (Uca mjoebergi). Furthermore, we show that distinct carapace colour patterns in Uca capricornis enable males to discriminate between their female neighbours and unfamiliar females. This is the first empirical evidence of the social importance of colour markings in fiddler crabs and the first example of visually mediated species and neighbour recognition in invertebrates other than insects.

SUMMARYNavigating animals are known to use a number of celestial and terrestrial compass cues that allow them to determine and control their direction of travel. Which of the cues dominate appears to depend on their salience. Here we show that night-active bull ants attend to both the pattern of polarised skylight and the landmark panorama in their familiar habitat. When the two directional cues are in conflict, ants choose a compromise direction. However, landmark guidance appears to be the primary mechanism of navigation used by forager ants, with those cues in the direction of heading having the greatest influence on navigation. Different colonies respond to the removal of these cues to different degrees, depending on the directional information provided by the local landmark panorama. Interestingly, other parts of the surrounding panorama also influence foraging speed and accuracy, suggesting that they too play a role in navigation.

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Animals are active at different times of the day and their activity schedules are shaped by competition, time-limited food resources and predators. Different temporal niches provide different light conditions, which affect the quality of visual information available to animals, in particular for navigation. We analysed caste-specific differences in compound eyes and ocelli in four congeneric sympatric species of Myrmecia ants, with emphasis on within-species adaptive flexibility and daily activity rhythms. Each caste has its own lifestyle: workers are exclusively pedestrian; alate females lead a brief life on the wing before becoming pedestrian; alate males lead a life exclusively on the wing. While workers of the four species range from diurnal, diurnal-crepuscular, crepuscular-nocturnal to nocturnal, the activity times of conspecific alates do not match in all cases. Even within a single species, we found eye area, facet numbers, facet sizes, rhabdom diameters and ocelli size to be tuned to the distinct temporal niche each caste occupies. We discuss these visual adaptations in relation to ambient light levels, visual tasks and mode of locomotion.

Animal signals are optimized for particular signaling environments [1-3]. While signaling, senders often choose favorable conditions that ensure reliable detection and transmission [4-8], suggesting that they are sensitive to changes in signal efficacy. Recent evidence has also shown that animals will increase the amplitude or intensity of their acoustic signals at times of increased environmental noise [9-11]. The nature of these adjustments provides important insights into sensory processing. However, only a single piece of correlative evidence for signals defined by movement suggests that visual-signal design depends on ambient motion noise [12]. Here we show experimentally for the first time that animals communicating with movement will adjust their displays when environmental motion noise increases. Surprisingly, under sustained wind conditions, the Australian lizard Amphibolurus muricatus changed the structure and increased the duration of its introductory tail flicking, rather than increasing signaling speed. The way these lizards restructure the alerting component of their movement-based aggressive display in the presence of increased motion noise highlights the challenge we face in understanding motion-detection mechanisms under natural operating conditions.