Stereoscopic corrugation detection in the presence of horizontal- and vertical- additive disparity noise was examined using a signal detection paradigm. Random-dot stereograms either represented a 3-D square-wave surface with various amounts of Gaussian-distributed additive disparity noise or had the same disparity values randomly redistributed. Stereoscopic detection of 2 arcmin peak amplitude...

Many neurons in the lateral-ventral region of the medial superior temporal area (MSTl) have a clear center surround separation in their receptive fields. Either moving or stationary stimuli in the surround modulates the response to moving stimuli in the center, and this modulation could facilitate the perceptual segmentation of a moving object from its background. Another mechanism that could f...

Vertical binocular disparity is a source of distance information allowing the portrayal of the layout and 3D metrics of the visual space. The role of vertical disparity in the perception of depth, size, curvature, or slant of surfaces was revealed in several previous studies using cue conflict paradigms. In this study, we varied the configuration of stereo-cameras to investigate how changes in ...

We address two unresolved issues concerning the coding of binocular disparity in primary visual cortex. Experimental studies and theoretical models have suggested a relationship between a cell's ocular dominance, assessed with monocular stimuli, and its tuning to binocular disparity. First, the disparity energy model of disparity selectivity suggests that there should be a correlation between o...

Using cortical source estimation techniques based on high-density EEG and fMRI measurements in humans, we measured how a disparity-defined surround influenced the responses to the changing disparity of a central disk within five visual ROIs: V1, V4, lateral occipital complex (LOC), hMT+, and V3A. The responses in the V1 ROI were not consistently affected either by changes in the characteristics...

Most neurons in primate visual area MT have a large, modulatory region surrounding their classically defined receptive field, or center. The velocity tuning of this "surround" is generally antagonistic to the center, making it potentially useful for detecting image discontinuities on the basis of differential motion. Because classical MT receptive fields are also disparity-selective, one might ...

As the disparity gradient of a stimulus increases, human observers’ ability to solve the correspondence problem and thereby estimate the disparities becomes poorer. It finally fails altogether when a critical gradient—the disparity-gradient limit (Burt & Julesz, 1980)—is reached. We investigated the cause of the disparity-gradient limit. As part of this work, we developed a local cross-correlat...

Editor's Note: These short, critical reviews of recent papers in the Journal, written exclusively by graduate students or postdoctoral fellows, are intended to summarize the important findings of the paper and provide additional insight and commentary. For more information on the format and purpose of the Journal Club, please see Review of Krug and Parker Binocular disparity results from the su...

This paper presents a technique for multi-channel optical ow estimation. We combine the brightness constancy constraint with the relationship between optical ow elds and disparity elds in estimating optical ow elds by solving systems of linear equations. In this formulation, the so called round-about compatibility constraint is used to ensure the coherence between optical ow elds and to pin dow...

Most neurophysiological accounts of disparity selectivity in neurons of the primary visual cortex (V1) imply that they are selective for absolute retinal disparities. By contrast, a number of psychophysical observations indicate that relative disparities play a more important role in depth perception. During recordings from disparity selective neurons in area V1 of awake behaving monkeys, we us...