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Neither occlusion constraint nor binocular disparity accounts for the perceived depth in the 'sieve effect'.

Current notions of binocular depth perception include (1) neural computations that solve the correspondence problem and calculate retinal positional disparity, and (2) recovery of ecologically valid occlusion relationships. The former framework works well for stimuli with unambiguous interocular correspondence, but less so for stimuli without well-defined disparity cues. The latter framework has been proposed to account for the phenomenon of perceived depth in stimuli without interocular correspondence, but its mechanism remains unclear. In order to obtain more insight into the mechanism, we studied the depth percept elicited by a family of stereograms - 'sieve' stimuli, adapted from Howard (1995) [Perception, 24, 67-74] - with interocular differences but no well-defined positional disparity cue. The perceived depth was measured by comparison to references at various depths established by standard retinal disparity and was consistently found to lie behind the fixation plane. Moreover, the magnitude of the depth percept depended on both the horizontal and vertical spatial characteristics of the stimulus in ways that were at odds with constraints of occlusion geometry. In comparison to the depth percept elicited by stimuli with well-defined disparity cues, the precision of the percept from the sieve stimuli was 10-20 times worse, suggesting that a different underlying computation was involved. Thus, neither of the above frameworks accounts for the depth percept arising from these stimuli. We discuss implications of our results for physiologically based computations underlying binocular depth perception.

Convergence, Ocular↗

[Vergence dynamics and variability of fixation disparity in school children with reading-spelling disorders].

BACKGROUND: New computer-controlled psychophysical procedures allow one to measure some temporal aspects of binocular coordination. The present study investigates whether these procedures can be operated by children and whether the tests are useful to detect previously reported impairments in dynamics and stability of vergence in children with disability in reading and writing. METHODS: To assess the variability in vergence accuracy (fixation disparity), a stationary fusion stimulus appeared on a computer monitor superimposed by short-term presentations of two dichoptic vertical nonius lines with varying horizontal offset. From the variability of the responses, a measure of vergence variability was deduced. Vergence velocity was estimated with nonius lines that appeared at a fixed delay of 400 ms after a sudden change in disparity of 30 minutes of arc. The full sample comprised 66 children, aged 7-16 years. 16 of these were not able to localize the nonius lines accurately in a control condition; therefore, these children were excluded from the following analysis. RESULTS: In the remaining 50 children, a group of 30 pupils with different aspects of disability in reading and writing had a nearly significant worse vergence performance both with respect to convergence velocity and to variability of fixation disparity (as compared to a control group of n = 20). These two findings corresponded to each other since convergence velocity and variability of fixation disparity were correlated. CONCLUSIONS: The results confirm previous reports and suggest further research on temporal aspects of vergence with respect to dyslexia. The computer-controlled test procedures are applicable in children of about 10 years or older.

Adolescent↗

Motion transparency promotes synchronous perceptual binding.

While identified regions of human extrastriate visual cortex are functionally specialized for processing different attributes of an object, the cognitive and neural mechanisms by which these attributes are dynamically bound into integrated percepts are still largely mysterious. Here, we report that perceptual organization influences the dynamics of binding. Specifically, the perception of motion transparency promotes the synchronous perceptual binding of colour and motion, which otherwise exhibits considerable asynchronies. In addition, we demonstrate that perceptual asynchrony can be reinstated by manipulating stereoscopic disparity or speed within the stimulus. Our findings suggest that the phenomenology of colour-motion binding parallels the known physiology of motion processing in area MT of primate visual cortex, supporting the view that the dynamics of perceptual binding is a direct reflection of the time course of the underlying neural processing.

Color Perception↗

Temporal aspects of spatial interactions affecting stereo-matching solutions.

Stereo-matching solutions minimize disparity relative to the horopter (minimum-absolute-disparity or MAD), and differences in disparity between adjacent features (minimum-relative-disparity or MRD). When placed in conflict, spatial proximity promotes MRD over MAD solutions. How does temporal proximity of neighboring features affect strength of these spatial interactions? We quantified the inter-stimulus interval (ISI) over which an unambiguous disparity pattern influenced stereo-matches for patterns with several possible solutions. Likelihood of MRD decreased as ISI increased (48.9 ms time constant) and increased as contrast was reduced for short ISIs, suggesting that monocular persistence (temporal impulse response) underlies the temporal interaction.

Contrast Sensitivity↗

Stereo channels with different temporal frequency tunings.

To investigate the spatial and temporal frequency tunings for stereopsis, we measured the contrast sensitivity for depth discrimination with variable spatiotemporal frequencies and disparities using drifting sinusoidal gratings. The results showed that the contrast sensitivity changed with the stimulus disparity and the disparity tuning function varied with the spatial frequency. The disparity in the peak sensitivity decreased proportionally with the spatial frequency (size-disparity correlation). Although the temporal frequency exhibited a limited influence on the peak disparity, the temporal frequency tuning varied with the spatial frequency. The shape of the temporal frequency tuning function was lowpass for higher spatial frequencies, whereas it was bandpass for low spatial frequencies. These results suggest that more than one channel with different temporal as well as spatial frequency tunings contribute to stereopsis.

Contrast Sensitivity↗

Monocular occlusion cues alter the influence of terminator motion in the barber pole phenomenon.

The influence of monocular occlusion cues on the perceived direction of motion of barber pole patterns is examined. Unlike previous studies that have emphasized the importance of binocular disparity, we find that monocular cues strongly influence the perceived motion direction and can even override binocular depth cues. The difference in motion bias for occluders with and without disparity cues is relatively small. Additionally, although 'T-junctions' aligned with occluders are particularly important, they are not strictly necessary for creating a change in motion perception. Finally, the amount of motion bias differs for several stimulus configurations, suggesting that the extrinsic/intrinsic classification of terminators is not all-or-none.

Contrast Sensitivity↗

Binocular cues and the control of prehension.

The present study was designed to assess the importance of binocular information (i.e. binocular disparity and angle of convergence) in the control of prehension. Previous studies which have addressed this question have typically used the same experimental manipulation: comparing prehensile movements executed either under binocular conditions to those executed when one eye was occluded (monocular). However this may not be the correct comparison as in addition to depriving the subject of binocular depth cues. it also deprives the subject of any visual information in one eye. Therefore we determined the prehensile performance when the subject viewed the target object and scene with either (i) two different views (binocular), (ii) two identical views (bi-ocular), or (iii) one view only (monocular). Overall, the qualitative and quantitative performance in the bi-ocular and monocular control conditions was very similar on all the main measures (and different from the performance in the binocular condition). We conclude that the deficits in performance observed found for 'monocular' reaches should be attributed to the lack of local depth information specified by the binocular cues. In addition we speculate that convergence angle and binocular disparity, although involved in both the pre-movement and movement-execution phases of the reach, the cues may be weighted differently in both phases of a prehension movement depending on the behavioural strategy involved.

Adult↗

Local disparity not perceived depth is signaled by binocular neurons in cortical area V1 of the Macaque.

Binocular neurons that are closely related to depth perception should respond selectively for stimuli eliciting an appropriate depth sensation. To separate perceived depth from local disparity within the receptive field, sinusoidal luminance gratings were presented within a circular aperture. The disparity of the aperture was coupled to that of the grating, thereby rendering unambiguous the psychophysical matching between repeating cycles of the grating. In cases in which the stimulus disparity differs by one horizontal period of the grating, the portion of the grating that locally covers a receptive field is binocularly identical, but the depth sensation is very different because of the aperture. For 117 disparity-selective V1 neurons tested in two monkeys, the overwhelming majority responded equally well to configurations that were locally identical but led to different perceptions of depth. Because the psychophysical sensation is not reflected in the firing rate of V1 neurons, the signals that make stereo matches explicit are most likely elaborated in extrastriate cortex.

Animals↗

Monocular components of the fixation disparity curve.

Experiments were conducted to characterize the distribution of the monocular components of fixation disparity, i.e., ascertain whether or not the fixation disparity measured by nonius alignments is equally divided between the two eyes or has an unequal distribution. Computer generated nonius lines were used to measure the monocular components of the forced vergence fixation disparity curve (FDC) for subjects with normal binocularity. Thirty-three percent of all subjects tested showed unequal distribution of their monocular components. The composite FDC's for subjects with unequal distribution of the monocular components tended to have steeper slopes than those with equally distributed components. It was concluded that equally divided monocular components are not a prerequisite for good binocularity.

Adult↗

Is prior knowledge of object geometry used in visually guided reaching?

We investigated whether humans use prior knowledge of the geometry of faces in visually guided reaching. When viewing the inside of a mask of a face, the mask is often perceived as being a normal (convex) face, instead of the veridical, hollow (concave) shape. In this "hollow-face illusion," prior knowledge of the shape of faces dominates perception, even when in conflict with information from binocular disparity. Computer images of normal and hollow faces were presented, such that depth information from binocular disparity was consistent or in conflict with prior knowledge of the geometry. Participants reached to touch either the nose or cheek of the faces or gave verbal estimates of the corresponding distances. We found that reaching to touch was dominated by prior knowledge of face geometry. However, hollow faces were estimated to be flatter than normal faces. This suggests that the visual system combines binocular disparity and prior assumptions, rather than completely discounting one or the other. When comparing the magnitude of the hollow-face illusion in reaching and verbal tasks, we found that the flattening effect of the illusion was similar for verbal and reaching tasks.

Cognition↗

Disparity capture by flanking stimuli: a measure for the cooperative mechanism of stereopsis.

In this work the range and scaling properties of the cooperative (contextual) interaction that was first proposed by Julesz [Foundations of Cyclopean Perception, University of Chicago Press, Chicago, 1971] to address the correspondence problem in stereopsis is measured. To this end the effect that flanking difference of Gaussians (DoG) patches produce on a perception of a target pair of patches is studied. The relative depth configuration of the target pair can switch from the small disparity gradient to a large disparity gradient state as a result of cooperative effects of the flanking stimuli. It is found that the interaction strength falls with distance. Its range varies for different subjects from 2 to 3 DoG patch sizes and scales proportionally to the size of the stimuli. The results suggest that a very localized cooperative interaction is in effect at a broad range of spatial scales.

Algorithms↗

Stereo and motion information are not independently processed by the visual system.

Many visual tasks are carried out by using multiple sources of sensory information to estimate environmental properties. In this paper, we present a model for how the visual system combines disparity and velocity information. We propose that, in a first stage of processing, the best possible estimate of the affine structure is obtained by computing a composite score from the disparity and velocity signals. In a second stage, a maximum likelihood Euclidean interpretation is assigned to the recovered affine structure. In two experiments, we show that human performance is consistent with the predictions of our model. The present results are also discussed in the framework of another theoretical approach of the depth cue combination process termed Modified Weak Fusion.

Cues↗

Noise causes slant underestimation in stereo and motion.

This paper discusses a problem, which is inherent in the estimation of 3D shape (surface normals) from multiple views. Noise in the image signal causes bias, which may result in substantial errors in the parameter estimation. The bias predicts the underestimation of slant found in psychophysical and computational experiments. Specifically, we analyze the estimation of 3D shape from motion and stereo using orientation disparity. For the case of stereo, we show that bias predicts the anisotropy in the perception of horizontal and vertical slant. For the case of 3D motion we demonstrate the bias by means of a new illusory display. Finally, we discuss statistically optimal strategies for the problem and suggest possible avenues for visual systems to deal with the bias.

Form Perception↗

Vergence eye movements in response to binocular disparity without depth perception.

Primates use vergence eye movements to align their two eyes on the same object and can correct misalignments by sensing the difference in the positions of the two retinal images of the object (binocular disparity). When large random-dot patterns are viewed dichoptically and small binocular misalignments are suddenly imposed (disparity steps), corrective vergence eye movements are elicited at ultrashort latencies. Here we show that the same steps applied to dense anticorrelated patterns, in which each black dot in one eye is matched to a white dot in the other eye, initiate vergence responses that are very similar, except that they are in the opposite direction. This sensitivity to the disparity of anticorrelated patterns is shared by many disparity-selective neurons in cortical area V1, despite the fact that human subjects fail to perceive depth in such stimuli. These data indicate that the vergence eye movements initiated at ultrashort latencies result solely from locally matched binocular features, and derive their visual input from an early stage of cortical processing before the level at which depth percepts are elaborated.

Convergence, Ocular↗

Binocular fusion limits are independent of contrast, luminance gradient and component phases.

Panum's binocular fusion limit has been shown to increase with the size of graded contrast targets (Schor, Wood & Ogawa, 1984). This suggests the hypothesis that the fusion limit may be controlled by the maximum luminance gradients present in the stimuli. The luminance gradient is reciprocally related to image contrast, so the hypothesis predicts that the fusion limits should also decrease with increasing contrast. To investigate this luminance gradient hypothesis we designed stimuli in which the contrast and phase of the spatial frequency components could be varied independently of the luminance gradients. Disparity limits for fusion were unaffected by variations of as much as a log unit in contrast, luminance gradient or phase of the frequency components, disconfirming the luminance gradient hypothesis. Instead, fusion limits for various compound frequency targets were well predicted by the smallest fusion range for any spatial frequency component in the image that was above its contrast detection threshold.

Contrast Sensitivity↗

Binocular unmasking with vertical disparity.

We recently found (Schneider, Moraglia, & Jepson, 1989) that the contrast threshold for the detection of a visual signal in a noisy background can be considerably lower when binocular cues are available then when monocular cues only are present. Here, we investigated the occurrence of binocular unmasking with vertical interocular disparities. Subjects reported about the presence of Gabor signals in fields of two-dimensional broadband Gaussian noise surrounded by a frame of uniform noise. They saw these stimuli through a stereoscope; in all cases, the right-eye noise field was vertically displaced relative to the left one in either an upward or a downward direction, by up to 67.6'. In one condition, the right-eye signal was displaced by an amount equal to that of the noise, so that no opportunities for binocular unmasking existed; in the other, it appeared in exactly corresponding locations in the two fields--here, binocular disparities could be used to unmask the signal. Enhanced signal detectability, by up to 12.7 dB, was observed in the latter case for both directions of displacement, but only for displacements of 13.52' and only when the signal's orientation was horizontal. We argue that these effects result from the summation of monocular inputs carried out by linear binocular mechanisms.

Adult↗

Rejection of false matches for binocular correspondence in macaque visual cortical area V4.

A plane lying in depth is vividly perceived by viewing a random-dot stereogram (RDS) with a slight binocular disparity. Perception of a plane-in-depth is lost by reversing the contrast of dots seen by one of the eyes to generate an anticorrelated RDS. From a computational perspective, the visual system cannot find a globally consistent solution for matching the left and right eye images of an anticorrelated RDS. The neural representation of a global match should therefore be insensitive to binocular disparity in an anticorrelated RDS. Most neurons in the striate cortex (V1) respond to binocular disparity in anticorrelated RDSs, suggesting that further cortical processing in extrastriate areas is necessary to fully account for the matching computation. We examined neural responses to dynamic RDSs, both normal (correlated) and anticorrelated, in area V4 of the monkey visual cortex. More than half of the V4 cells were sensitive to the horizontal disparity embedded in a correlated RDS. Most of them greatly attenuated their selectivity for disparity when the RDS was anticorrelated. This attenuation was apparent from the response onset, and the degree of attenuation did not correlate with neuronal response latencies. Unlike the disparity tuning of V1 neurons to anticorrelated RDSs, that of V4 neurons was not an inversion of tuning to normal RDSs. Our results suggest that responses to false matches between contrast-reversed dots in the left and right eye images elicited in V1 are substantially reduced by the stage of V4.

Action Potentials↗

[Peculiarities of stereovision in children].

OBJECTIVE: The aim of this work was to evaluate the stereovision and the stereoacuity of the preschool children and to compare various stereotests. MATERIAL AND METHODS: The test group consisted of 118 children who were divided into 3 age groups: 2-3 year-old group (22.03%), 4-5 year-old group (43.22%) and 6-7 year-old group (34.75%). Titmus, Lang I and contour anaglyphic pictures stereotests were used. RESULTS: The stereovision was investigated in 94.92% of children (88.46% in 2-3 year old group, 96.08% in 4-5 years and 97.56% in 6-7 year-old group). The stereoacuity of 40" was detected in 63.41% of 6-7 year-old and only in 7.69% of 2-3 year-old children. CONCLUSIONS: A reverse correlation was noticed between the stereoacuity and the frequency of positive results in all age groups. The frequency of positive stereovision in various disparity levels and the stereoacuity increase together with the age of children; these data were significant between the groups of 2-3 years and 6-7 years (p<0.05). Data did not show significant differences between various stereotests, but we noticed that contoured stereotests were more comprehensible to the 2-5 year-old children.

Age Factors↗