The visual systems of insects are exquisitely sensitive to motion. Over the past 40 years or so, motion processing in insects has been studied and characterised primarily through the optomotor response. This response, which is a turning response evoked by the apparent movement of the visual environment, serves to stabilise the insect's orientation with respect to the environment. Research over the past decade, however, is beginning to reveal the existence of a variety of other behavioural responses in insects, that use motion information in different ways. Here we review some of the recently characterised behaviours, describe the inferred properties of the underlying movement-detecting processes, and propose modified or new models to account for them.

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Insects are frequently assumed to have hard-wired nervous systems that fail to demonstrate functional plasticity. We have produced changes in synaptic frequency, and analysed their developmental time course, dynamics and reversibility, in the lamina underlying the compound eye of the fly, by exposing young adults to different visual stimuli. The class of synapse examined feeds back from L2, one of the monopolar cells found in each lamina cartridge, to photoreceptor terminals; each site is a synaptic dyad marked by the presence of a few, round vesicles surrounding a T-shaped presynaptic ribbon and, in the photoreceptor, by a subsynaptic vacuole. In control adult flies reared in normal room lighting, the frequency of synaptic profiles scored in micrographs of single sections initially increased until one day post-eclosion (E + 1), but declined thereafter. Frequencies measured in left and right eyes of the same control animals were closely matched. Experimental flies were put for one to two days into an integrating sphere illuminated continuously with square-wave, 25 Hz green light. They had one eye occluded, so providing control comparisons between flicker-reared (FR) and occluded (dark-reared, DR) eyes within the same animal. The DR eyes invariably (n greater than 22) had higher frequencies of synaptic profiles than those seeing light, regardless of age or the period of light exposure, although the detailed relative effects of FR and DR depend upon the age of the animal. The evidence suggests that exposure to light actively depresses synaptic frequency and increases its variability. The greatest difference (30%) achieved was at two to four days after eclosion and there was no difference beyond six days, so demarcating a prospective sensitive period. Rearing in DC light was equally effective as FR, so visual contrasts per se are apparently inessential. Frequency values can change rapidly. During the first 24 h post-eclosion, DR resulted in new synapses adding to L2's complement of 25-35 at a maximum rate of 4 per 6 h, whereas light exposure caused a frequency decrease after as little as 6 h. Alternating 24 h periods of light and dark during the first two days produced reversible synaptic frequency changes. Individual synaptic contacts enlarge with age but not significantly with different visual experiences. The decrease in frequency of synaptic profiles with age thus actually underestimates the true decrease in synaptic number, whereas the altered synaptic frequencies seen after differential exposure represent true differences in synaptic number.(ABSTRACT TRUNCATED AT 400 WORDS)

Abstract. The aim of this review is to explain the functional significance of mantis peering behaviour from an entomological perspective. First the morphological and optical features of the mantis compound eye that are important for spatial vision are described. The possibility that praying-mantises use binocular retinal disparity (stereopsis) and other alternative visual cues for determining distance in prey capture, are discussed. The primary focus of the review is the importance of peering movements for estimating the distance to stationary objects. Here the following aspects are examined: (1) Direct evidence via object manipulation experiments of absolute distance estimation with the aid of self-induced retinal image motion; (2) the mechanism of absolute distance estimation (with the interaction of visual and proprioceptive information); (3) the range of absolute and relative distance estimation; (4) the influence of target object features on distance estimation; and (5) the relationship between peering behaviour and habitat structures, based on results of studies on three species of mantis.

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Abstract. Mantispids (Neuroptera: Mantispidae) are remarkable insects as a result of their close resemblance to the praying mantis (order Mantodea). Although not closely related phylogenetically, as a result of similar selective pressures, both mantispids and mantids have evolved powerful raptorial forelegs for capturing insects. Another striking feature is the hypermetamorphosis in mantispid development, as well as the parasitizing behaviour of the first-instar larvae. The present review focuses on the role of mantispid vision. First, the morphology and functional significance of the larval eyes (stemmata) are examined. In principle, the stemmata are suitable for spatial vision because of their arrangement and structure. This is then followed by a discussion of how adult mantispids are able to capture fast-moving insects successfully, although, in contrast to the praying mantis, mantispids rely on superposition eyes rather than on apposition eyes with a frontal region of high acuity. For both larvae and adults, comparisons are made with other insect groups. The present review also addresses the role of mantispid vision as an important cue for triggering mating behaviour; accordingly, sex-specific differences are considered. Finally, vision in the context of orientation flight is discussed.