The present study employs a stereoscopic manipulation to present sentences in three dimensions to subjects as they read for comprehension. Subjects read sentences with (a) no depth cues, (b) a monocular depth cue that implied the sentence loomed out of the screen (i.e., increasing retinal size), (c) congruent monocular and binocular (retinal disparity) depth cues (i.e., both implied the sentenc...

Judgments of visual depth rely crucially on the relative binocular disparity between two visual features. While areas of ventral visual cortex contain neurons that signal the relative disparity between spatially adjacent visual features, the same tests in dorsal visual areas yield little evidence for relative disparity selectivity. We investigated the sensitivity of neurons in dorsal visual are...

Estimating depth from binocular disparity is extremely precise, and the cue does not depend on statistical regularities in the environment. Thus, disparity is commonly regarded as the best visual cue for determining 3D layout. But depth from disparity is only precise near where one is looking; it is quite imprecise elsewhere. Away from fixation, vision resorts to using other depth cues-e.g., li...

Performing a visually guided reach requires the ability to perceive the egocentric distance of a target in three-dimensional space. Previous studies have shown that the parietal reach region (PRR) encodes the two-dimensional location of frontoparallel targets in an eye-centered reference frame. To investigate how a reach target is represented in three dimensions, we recorded the spiking activit...

A computational model for the control of horizontal vergence, based on a population of disparity tuned complex cells, is presented. The model directly extracts the disparity-vergence response by combining the outputs of the disparity detectors without explicit calculation of the disparity map. The resulting vergence control yields to stable fixation and has small response time to a wide range o...

Neurons in the visual cortex of monkeys respond selectively to the disparity between the images in the two eyes. Recent recordings have shown that some of the disparity-selective neurons in the primary visual cortex and the posterior parietal cortex are modulated by the distance of fixation. A population of such gain-modulated, disparity-selective neurons forms a set of basis functions of horiz...

The classic increment disparity threshold function rises steeply, usually exponentially, with disparity pedestal. Thus a smaller difference in stereoscopic depth can be resolved the nearer it is to the fixation plane. This result has been obtained with relatively broad-bandwidth stimuli. We show here that the increment threshold function for narrow-bandwidth stimuli differs subtly from the clas...

PURPOSE We evaluated the roles of luminance and fixation in the pathophysiology of dissociated vertical divergence (DVD). METHODS Vertical eye position was measured in 6 subjects with DVD (ages 11-47 years, 5 females) and 6 controls (ages 16-40 years, 5 females) using video-oculography (VOG) under conditions of change in fixation and luminance. RESULTS Subjects with DVD showed the following...

This paper presents an architecture for computing vector disparity for active vision systems as used on robotics applications. The control of the vergence angle of a binocular system allows us to efficiently explore dynamic environments, but requires a generalization of the disparity computation with respect to a static camera setup, where the disparity is strictly 1-D after the image rectifica...