Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Vision Disparity”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 73 records · Page 4Linked to original sources

Contour curvature polarity and surface interpolation.

Contour curvature polarity (i.e., concavity/convexity) is recognized as an important factor in shape perception. However, current interpolation models do not consider it among the factors that modulate the trajectory of amodally-completed contours. Two hypotheses generate opposite predictions about the effect of contour polarity on surface interpolation. Convexity advantage: if convexities are preferred over concavities, contours of convex portions should be more extrapolated than those of concave portions. Minimal area: if the area of amodally-completed surfaces tends to be minimized, contours of convex portions should be less extrapolated than contours of concave portions. We ran three experiments using two methods, simultaneous length comparison and probe localization, and different displays (pictures vs. random dot stereograms). Results indicate that contour polarity affects the amodally-completed angles of regular and irregular surfaces. As predicted by the minimal area hypothesis, image contours are less extrapolated when the amodal portion is convex rather than concave. The field model of interpolation [Fantoni, C., & Gerbino, W. (2003). Contour interpolation by vector-field combination. Journal of Vision, 3, 281-303. Available from http://journalofvision.org/3/4/4/] has been revised to take into account surface-level factors and to explain area minimization as an effect of surface support ratio.

Adult↗

Contrast sensitivity of form and motion discrimination during binocular rivalry.

Binocular rivalry, which is induced by presenting the two eyes with incompatible stimuli, results in periods where one eye's stimulus is seen and the other stimulus is suppressed. We measured the depth of suppression in two ways, with very different results. First, two similar forms were briefly presented to one eye: the difference in shapes required to discriminate the forms was substantially greater during suppression than during dominance. Second, the two forms were made sufficiently different in shape to be easily distinguishable at high contrast, and contrast was lowered to find the threshold for discrimination of the forms. Contrast sensitivity did not differ between the suppression and dominance states. These results were replicated with a motion discrimination task: suppression markedly worsened the ability to distinguish increases from decreases in speed but did not elevate the minimum contrast required for the same task. We interpret the results in terms of steep contrast-response functions in visual cortex beyond the primary area.

Adult↗

Absolute travel distance from optic flow.

Optic flow fields provide rich information about the observer's self-motion. Besides estimation of the direction of self-motion human observers are also able to discriminate the travel distances of two self-motion simulations. Recent studies have shown that observers estimate the simulated ego velocity of the self-motion simulation and integrate it over time. Thus, observers use a 3-D percept of the ego motion through the environment. In the present work we ask if human observers are able to use this 3-D percept of the motion simulation to build up an internal representation of travel distance and indicate it in a static scene. We visually simulated self-motion in different virtual environments and asked subjects to indicate the perceived distances in terms of static virtual intervals on the ground. The results show that human observers possess a static distance gauge, but that they undershoot the travel distances for short motion simulations. In further experiments we changed the modality of the distance indication but the undershoot in distance estimation remained. This suggests that the undershoot is linked to the perception of the optic flow field.

Cues↗

Stereoscopic depth aftereffects without retinal position correspondence between adaptation and test stimuli.

To clarify whether stereo-slant aftereffects are independent of stimulated retinal position, two experiments compared the magnitude of aftereffects between the following two conditions: when the adaptation and test stimulus fell on (1) the same retinal position, and (2) on different retinal positions separated by 0.5 degrees -20 degrees . In Experiment 1, disc- or ring-shaped surface consisting of random-dots was presented at the central or peripheral visual fields. In Experiment 2, rectangular surface was presented at the upper or lower visual fields. After two minutes inspection of a random-dot stereogram depicting a +/-30 degrees slanted surface, the observer adjusted the slant of the test stimulus to appear fronto-parallel. The results of the experiments showed that significant aftereffects were observed similarly in both conditions. Moreover, the separation nor the stimulus shape scarcely affected the magnitude of the aftereffects. Based on these results we concluded that the depth processing mechanism which operates independently from the stimulated retinal position is responsible for the depth aftereffects we found.

Adaptation, Physiological↗

A binocular rivalry study of motion perception in the human brain.

The relationship between brain activity and conscious visual experience is central to our understanding of the neural mechanisms underlying perception. Binocular rivalry, where monocular stimuli compete for perceptual dominance, has been previously used to dissociate the constant stimulus from the varying percept. We report here fMRI results from humans experiencing binocular rivalry under a dichoptic stimulation paradigm that consisted of two drifting random dot patterns with different motion coherence. Each pattern had also a different color, which both enhanced rivalry and was used for reporting which of the two patterns was visible at each time. As the perception of the subjects alternated between coherent motion and motion noise, we examined the effect that these alternations had on the strength of the MR signal throughout the brain. Our results demonstrate that motion perception is able to modulate the activity of several of the visual areas which are known to be involved in motion processing. More specifically, in addition to area V5 which showed the strongest modulation, a higher activity during the perception of motion than during the perception of noise was also clearly observed in areas V3A and LOC, and less so in area V3. In previous studies, these areas had been selectively activated by motion stimuli but whether their activity reflects motion perception or not remained unclear; here we show that they are involved in motion perception as well. The present findings therefore suggest a lack of a clear distinction between 'processing' versus 'perceptual' areas in the brain, but rather that the areas involved in the processing of a specific visual attribute are also part of the neuronal network that is collectively responsible for its perceptual representation.

Adult↗

The motion-induced position shift depends on the visual awareness of motion.

Visual motion signals distort the perceived positions of briefly presented stimuli; a briefly-flashed, stationary stimulus appears spatially displaced in the direction of a nearby motion. The present study examined the role of the visual awareness of motion in the motion-induced position shift by using exclusive dominance and suppression of binocular rivalry. Observers dichoptically viewed a flickering radial checkerboard and two sinusoidal gratings that drifted vertically in opposite directions. When observers viewed exclusively either the checkerboard or motion stimulus, two horizontal lines were flashed, one for each side of the rivalry stimulus. During the exclusive dominance of the grating motion, the lines appeared to shift in the directions of the nearby motions. The position shift was identical to that during non-rivalry, monocular viewing of the motion stimulus. However, when the grating motions were completely suppressed, no position shift was observed. These results demonstrate that the motion-induced position shift depends on the visual awareness of motion.

Awareness↗

Interactions between binocular rivalry and Gestalt formation.

A question raised a long time ago in binocular rivalry research is whether the phenomenon of binocular rivalry is purely determined by local stimulus properties or that global stimulus properties also play a role. More specifically: do coherent features in a stimulus influence rivalrous behavior? After decades of underexposure of the subject, recently this question seemed to be answered in the affirmative. This paper presents additional evidence for an influence of coherent features. In an experiment in which eye movements cannot bias conclusions it is demonstrated that Gestalt formation influences binocular rivalry positively, i.e., stronger Gestalts have longer total dominance times. Gestalt formation appears to intervene in the states of dominance ("what"), not directly in the dominance durations ("how long"). This generates questions about the nature of interactions between binocular rivalry and Gestalt formation. Gestalt formation seems to be fed by signals that are generated after binocular convergence and only leaves its mark on binocular rivalry by feedback to monocular channels, a conclusion which has been drawn before by Alais and Blake [Alais, D., & Blake, R. (1998). Interaction between global motion and local binocular rivalry. Vision research 38, 637-644].

Adult↗

The cyclopean eye is relevant for predicting visual direction.

Wells-Hering's laws summarize how we process direction and predict that monocular stimuli appear displaced with respect to the viewer, but not with respect to other seen objects [Erkelens, C. J., & van Ee, R. (2002). The role of the cyclopean eye in vision: sometimes inappropriate, always irrelevant. Vision Research 42, 1157-1163] criticized this view and claimed that there is no perceptual displacement of these stimuli. We challenge their claim and improve on shortcomings of past studies. LEDs were monocularly presented to the observers, without their knowledge of which eye was being stimulated. Viewing distance was 9-10 cm; fixation distance was 30 cm. Observers reported the perceived relative and absolute directions of monocular stimuli. Our results are consistent with Wells-Hering's laws.

Awareness↗

Center-surround inhibition deepens binocular rivalry suppression.

When dissimilar stimuli are presented to each eye, perception alternates between both images--a phenomenon known as binocular rivalry. It has been shown that stimuli presented in proximity of rival targets modulate the time each target is perceptually dominant. For example, presenting motion to the region surrounding the rival targets decreases the predominance of the same-direction target. Here, using a stationary concentric grating rivaling with a drifting grating, we show that a drifting surround grating also increases the depth of binocular rivalry suppression, as measured by sensitivity to a speed discrimination probe on the rival grating. This was especially so when the surround moved in the same direction as the grating, and was slightly weaker for opposed directions. Suppression in both cases was deeper than a no-surround control condition. We hypothesize that surround suppression often observed in area MT (V5)-a visual area implicated in visual motion perception-is responsible for this increase in suppression. In support of this hypothesis, monocular and binocular surrounds were both effective in increasing suppression depth, as were surrounds contralateral to the probed eye. Static and orthogonal motion surrounds failed to add to the depth of rivalry suppression. These results implicate a higher-level, fully binocular area whose surround inhibition provides an additional source of suppression which sums with rivalry suppression to effectively deepen suppression of an unseen rival target.

Humans↗

Adaptive center-surround interactions in human vision revealed during binocular rivalry.

We used binocular rivalry as a psychophysical probe to explore center-surround interactions in orientation, motion and color processing. Addition of the surround matching one of the rival targets dramatically altered rivalry dynamics. For all visual sub-modalities tested, predominance of the high-contrast rival target matched to the surround was greatly reduced-a result that disappeared at low contrast. At low contrast, addition of the surround boosted dominance of orientation and motion targets matched to the surround. This contrast-dependent modulation of center-surround interactions seems to be a general property of the visual system and may reflect an adaptive balance between surround suppression and spatial summation.

Color Perception↗

Independent binocular integration for form and colour.

Although different features of an object are processed in anatomically distinct regions of the cerebral cortex, they often appear bound together in perception. Here, using binocular rivalry, we reveal that the awareness of form can occur independently from the awareness of colour. First, we report that, if both eyes briefly view a grating stimulus prior to the presentation of the same grating in one eye and an orthogonal grating in the other, subjects tend to report perceptual dominance of the non-primed grating. The primer was most effective when it was similar in orientation, spatial frequency and spatial phase to one of the rival images. Next, we showed that the process underlying the binocular integration of chromatic information was selectively influenced by the colour of a previously presented stimulus. We then combined these paradigms by using a primer that had the same colour as one rival stimulus, but the same form as the other stimulus. In this situation, we found that rival stimuli differing in form and colour can sometimes achieve states of dominance in which the chromatic information from one eye's image combines with the form of the other eye's image temporarily creating a binocular impression that corresponds with neither monocular component. Finally, we demonstrated that during continuous viewing of rival stimuli differing in form and colour, chromatic integration could occur independently of form rivalry. Paradoxically, however, we found that changes to the form of the stimulus had more of an influence on chromatic integration than on form rivalry. Together these phenomena show that the neural processes involved in integrating information from the two eyes can operate selectively on different stimulus features.

Color Perception↗

Competition in bistable vision is attribute-specific.

We employ ambiguous figures and rivalrous stimuli that have multiple ambiguous properties to show that the different attributes of an ambiguous stimulus can undergo independent switching dynamics. This suggests that competition is distributed and attribute-specific, consistent with the known functional segregation of visual processing. Conflicting evidence that binocular rivalry is an early or late visual process may be better understood as evidence for attribute-specific competition occurring at multiple stages of visual processing. Specifically, we show that whether perceptual selection during binocular rivalry is early and eye-based or late and percept-based depends on the particular ambiguous attributes of the rivalrous stimulus.

Humans↗

The orientation bandwidth of cyclopean channels.

Orientation bandwidths of cyclopean channels were estimated using a notched noise technique. Observers were presented with random dot stereograms depicting a horizontal or vertical target sinusoidal depth modulation and a mask consisting of sinusoidal depth modulations whose orientations flanked that of the target. Masking reduced as the orientation difference between signal and mask increased. The orientation bandwidth of the masking effect was similar to that found for stimuli defined by luminance contrast, and showed no systematic difference for horizontal and vertical targets. These results suggest that the elongated summation found by Tyler, C. W., and Kontsevich, L. L. (2001). Stereoprocessing of cyclopean depth images: Horizontally elongated summation fields. Vision Research, 41, 2235-2243, for horizontal stimuli occurs after a processing non-linearity.

Depth Perception↗

Monocular texture segmentation and proto-rivalry.

When the right eye's target is the left eye's distracter and vice versa, orientation-defined search is impossible unless, as we show here, the elements are close together. More than 1s was required to find inverse-cyclopean texture boundaries when elements were arranged on a 16 x 16 grid. Less than 250 ms was required for a 24 x 24 grid covering the same area. The conventional view is that binocular rivalry requires at least 200 ms to develop, but our results suggest a more rapid access to monocular signals. We call this rapid form of access "proto-rivalry."

Eye Movements↗

A long-distance stereoscopic detector for partially occluding surfaces.

An external noise technique was used to investigate the stereoscopic process that generates an illusory phantom occluder from binocularly unmatched elements. Observers were required to identify the quadrant in which a binocularly defined target was presented. We had three targets: (a) two vertical binocular bars with the unmatched portions arranged to induce a stable phantom occluder (valid), (b) the same stimuli except the image for the left eye was switched with that for the right eye therefore not inducing a stable occluder (invalid), and (c) a single binocular bar with the same unmatched portion (single-bar). For each target, the luminance contrast of the signal required for 75% correct responses was measured at four levels of external interocular noise. Contrast thresholds were found to be lower for the valid target than for both the invalid and the single-bar targets. The results suggest that the visual system has a stereoscopic detector that responds to stimuli that meet a long-distance requirement for the perception of partially occluding surfaces.

Form Perception↗

Pictorial cues constrain depth in da Vinci stereopsis.

"da Vinci stereopsis" is defined as depth seen in a monocular object occluded by a binocular one, and the visual system must solve its depth ambiguity [Nakayama, K., & Shimojo, S. (1990). da Vinci stereopsis: Depth and subjective occluding contours from unpaired image points. Vision Research, 30, 1811-1825]. Although fused images include various pictorial features, effects of pictorial depth cues have never been systematically investigated in da Vinci stereopsis. To examine this, we created stereograms consisting of a monocular bar flanked by binocular bars with a fixed large horizontal separation, in which the monocular bar induced a subjective occluding edge. Manipulating vertical size or contrast of the bars could affect the depth of the monocular bar. Conflicting these cues revealed that the effect of vertical size was stronger than that of contrast in all our subjects. Measurements of the depth indicated that the relative vertical size of the bars quantitatively determined the perceived depth, of which levels had large inter-subject differences. All these experiments indicate that the visual system can use the pictorial depth cues as a constraint to determine the depth of monocular elements.

Cues↗

Effect of decorrelation on 3-D grating detection with static and dynamic random-dot stereograms.

Three experiments examined the effects of image decorrelation on the stereoscopic detection of sinusoidal depth gratings in static and dynamic random-dot stereograms (RDS). Detection was found to tolerate greater levels of image decorrelation as: (i) density increased from 23 to 676 dots/deg2; (ii) spatial frequency decreased from 0.88 to 0.22 cpd; (iii) amplitude increased above 0.5 arcmin; and (iv) dot lifetime decreased from 1.6s (static RDS) to 80 ms (dynamic RDS). In each case, the specific pattern of tolerance to decorrelation could be explained by its consequences for image sampling, filtering, and the influence of depth noise.

Adult↗

The role of saccades in exerting voluntary control in perceptual and binocular rivalry.

We have investigated the role of saccades and fixation positions in two perceptual rivalry paradigms (slant rivalry and Necker cube) and in two binocular rivalry paradigms (grating and house-face rivalry), and we compared results obtained from two different voluntary control conditions (natural viewing and hold percept). We found that for binocular rivalry, rather than for perceptual rivalry, there is a marked positive temporal correlation between saccades and perceptual flips at about the moment of the flip. Across different voluntary control conditions the pattern of temporal correlation did not change (although the amount of correlation did frequently, but not always, change), indicating that subjects do not use different temporal eye movement schemes to exert voluntary control. Analysis of the fixation positions at about the moment of the flips indicates that the fixation position by itself does not determine the percept but that subjects prefer to fixate at different positions when asked to hold either of the different percepts.

Depth Perception↗