RESUMO
Neurons which respond selectively to small moving targets, even against a cluttered background, have been identified in several insect species. To investigate what underlies these robust and highly selective responses, researchers have probed the neuronal circuitry in target-detecting, visual pathways. Observations in flies reveal nonlinear adaptation over time, composed of a fast onset and gradual decay. This adaptive processing is seen in both of the independent, parallel pathways encoding either luminance increments (ON channel) or decrements (OFF channel). The functional significance of this adaptive phenomenon has not been determined from physiological studies, though the asymmetrical time course suggests a role in suppressing responses to repetitive stimuli. We tested this possibility by comparing an implementation of fast adaptation against alternatives, using a model of insect 'elementary small target motion detectors'. We conducted target-detecting simulations on various natural backgrounds, that were shifted via several movement profiles (and target velocities). Using performance metrics, we confirmed that the fast adaptation observed in neuronal systems enhances target detection against a repetitively moving background. Such background movement would be encountered via natural ego-motion as the insect travels through the world. These findings show that this form of nonlinear, fast-adaptation (suitably implementable via cellular biophysics) plays a role analogous to background subtraction techniques in conventional computer vision.