Motion-defined contour processing in the early visual cortex
Author(s) -
Amol Gharat,
Curtis L. Baker
Publication year - 2012
Publication title -
journal of neurophysiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.302
H-Index - 245
eISSN - 1522-1598
pISSN - 0022-3077
DOI - 10.1152/jn.00840.2011
Subject(s) - luminance , receptive field , artificial intelligence , computer vision , motion perception , contrast (vision) , visual cortex , orientation (vector space) , motion (physics) , parallax , spatial frequency , computer science , optics , physics , communication , neuroscience , psychology , mathematics , geometry
From our daily experience, it is very clear that relative motion cues can contribute to correctly identifying object boundaries and perceiving depth. Motion-defined contours are not only generated by the motion of objects in a scene but also by the movement of an observer's head and body (motion parallax). However, the neural mechanism involved in detecting these contours is still unknown. To explore this mechanism, we extracellularly recorded visual responses of area 18 neurons in anesthetized and paralyzed cats. The goal of this study was to determine if motion-defined contours could be detected by neurons that have been previously shown to detect luminance-, texture-, and contrast-defined contours cue invariantly. Motion-defined contour stimuli were generated by modulating the velocity of high spatial frequency sinusoidal luminance gratings (carrier gratings) by a moving squarewave envelope. The carrier gratings were outside the luminance passband of a neuron, such that presence of the carrier alone within the receptive field did not elicit a response. Most neurons that responded to contrast-defined contours also responded to motion-defined contours. The orientation and direction selectivity of these neurons for motion-defined contours was similar to that of luminance gratings. A given neuron also exhibited similar selectivity for the spatial frequency of the carrier gratings of contrast- and motion-defined contours. These results suggest that different second-order contours are detected in a form-cue invariant manner, through a common neural mechanism in area 18.
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