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Depth in anticorrelated stereograms: effects of spatial density and interocular delay.

Disparity-based depth is not perceived in densely textured, anticorrelated random-dot stereograms (RDSs) whose elements carry opposite signs of brightness contrast on corresponding loci, as extant data show. We observed global depth in anticorrelated RDSs flashed repetitively with an interocular delay. During the delay time, a dot array in one eye was paired with a gray frame in the other eye and thus could interact with the negative afterimage of the contralateral dot array. A correlated RDS (e.g. 8 min arc dots, 50% density, 15-msec flash duration) lost depth with delays > 45 msec. An anticorrelated RDS, that was otherwise identical, showed robust depth when flashed with an interocular delay of some 60 msec. A delay was not always necessary to produce depth. At low dot density (1-2%), anticorrelated RDSs showed disparity-dependent local depth even when displayed continuously, or flashed simultaneously; as dot density alone was increased, depth was progressively lost. To make global depth visible in a dense RDS flashed with an interocular delay, the internal response had to be strongly biphasic. Our results support the generally held notion that cyclopean depth signals emerge exclusively from same-sign binocular cortical filters. However, the exclusionary rule may be invalid with respect to the processing of coarse local depth with figural stimuli. Relative depth between a pair of small dots was easily perceived when one of the dots was in opposite contrast, but the depth threshold was then about 0.5 log unit higher than with the same-contrast pair of dots indicating that the internal effects of contrast have not all lost their sign prior to binocular disparity processing. It remains to be determined whether depth can be perceived from edges of opposite contrast.

Afterimage↗

Temporal aspects of slant and inclination perception.

Linear transformations (shear or scale transformations) of either horizontal or vertical disparity give rise to the percept of slant or inclination. It has been proposed that the percept of slant induced by vertical size disparity, known as Ogle's induced-size effect, and the analogous induced-shear effect, compensate for scale and shear distortions arising from aniseikonia, eccentric viewing, and cyclodisparity. We hypothesised that these linear transformations of vertical disparity are processed more slowly than equivalent transformations of horizontal disparity (horizontal shear and size disparity). We studied the temporal properties of the stereoscopic slant and inclination percepts that arose when subjects viewed stereograms with various combinations of horizontal and vertical size or shear disparities. We found no evidence to support our hypothesis. There were no clear differences in the build-up of percepts of slant or inclination induced by step changes in horizontal size or shear disparity and those induced by step changes in vertical size or shear disparity. Perceived slant and inclination decreased in a similar manner with increasing temporal frequency for modulations of transformations of both horizontal and vertical disparity. Considerable individual differences were found and several subjects experienced slant reversal, particularly with oscillating stimuli. An interesting finding was that perceived slant induced by modulations of dilation disparity was in the direction of the vertical component. This suggests the vertical size disparity mechanism has a higher temporal bandwidth than the horizontal size disparity mechanism. However, conflicting perspective information may play a dominant role in determining the temporal properties of perceived slant and inclination.

Form Perception↗

A dynamic model of cross-coupling between accommodation and convergence: simulations of step and frequency responses.

The near triad consists of an increase in accommodation, vergence, and pupillary constriction. All three motor systems exhibit phasic and tonic responses. The tonic response adapts readily to phasic efforts of accommodation and vergence. Cross-coupling between accommodation and vergence provides a means of dynamically adjusting the tonic set points of the two motor systems to a common near or far working distance. Accommodative vergence cross-links play a dominant role in coordinating proximal changes in accommodation and convergence. The magnitude of cross-link interactions can be modified by imbalanced strength of tonic adaptation by accommodation and vergence. Reducing adaptation of tonic accommodation increases the AC/A ratio and decreases the CA/C ratio. Reducing adaptation of tonic vergence has the opposite effect. A model is able to predict these and other interactions simply by reducing the decay time constant of one of the two motor systems. For example, reducing the time constant for tonic accommodation results in an increased AC/A ratio and decreased CA/C ratio. Reducing the time constant for tonic vergence has the opposite effect. The model predicts transient step responses by accommodative vergence when the AC/A ratio is low and transient step responses of vergence accommodation when the CA/C ratio is low. It also predicts a reciprocal relationship between the AC/A and CA/C ratios. When one cross-link ratio is high the other cross-link ratio is low. Simulated frequency responses predict the low frequency roll off of low AC/A and low CA/C ratios. The step and frequency responses of cross-link ratios are shown to be the same for proximal (perceived distance) and retinal (blur and disparity) stimuli. The model suggests that physiological variations of tonic decay time constants may play an important role in determining clinically abnormal values of AC/A and CA/C ratios.

Accommodation, Ocular↗

Central and peripheral visual interactions in disparity-induced vergence eye movements: I. Spatial interaction.

PURPOSE: To evaluate the interaction between central and peripheral disparities in the initiation of vergence eye movements. METHODS: Eye movements were recorded in eight normal subjects using an infrared limbus tracker. Three-dimensional visual stimuli were back projected onto a tangent screen by using two liquid crystal display (LCD) projectors through crossed polarizers. The central target was a vertical bar, which always jumped from 2 to 1 m. The peripheral target was a random-dot pattern that jumped from 2 to 0.75, 1, or 1.5 m (near planes), 2 m (no change), or 3 m (far plane) simultaneously with the central target jump. Latency, amplitude at 150 ms, and average amplitude over 1 to 2 seconds after vergence onset; peak velocity; and the main-sequence relationship of the initial vergence response were calculated. How far the central target appeared to jump was scored subjectively. RESULTS: In half of the subjects, there was a clear effect of the peripheral disparity on the dynamics of the vergence response to the central disparity. The amplitude of vergence at 150 ms, as an index of open-loop gain, was significantly greater when the peripheral target moved closer, but steady state amplitude (average during 1-2 seconds) did not change, and the vergence latency was significantly greater when the peripheral target jumped away. There was no obvious relationship between the perceived amount of movement of the central target and the parameters of the dynamic properties of the vergence response. CONCLUSIONS: Peripheral disparity can modulate the dynamics of the initial vergence response to a central disparity and is probably independent of the perception of motion in depth.

Adult↗

Fusional vergence in microstrabismus.

The fusional vergence velocity was studied in microstrabismus and in normal persons. In microstrabismus the system works less precisely in that small changes in disparity produce no response, while it is possible that the difference between the amplitude of the stimulus and the amplitude of the response is greater.

Eye Movements↗

Compensation procedures for the anisometropic presbyope.

When changing to bifocal lenses from distance anisometropic lenses, presbyopic patients may experience diplopia when attempting to do close work. Prescription failure can be dramatically reduced by utilizing the procedures outlined in this article. Why would a patient experience diplopia when attempting to read with bifocals? The diplopia may simply be a result of the optical difference in power between the two lenses. Anisometropia creates a disparity in the size of the retinal image as well as a prismatic imbalance when looking away from the optical center. A practical approach to coping with these problems is recommended.

Accommodation, Ocular↗

Quantitative characterization of disparity tuning in ventral pathway area V4.

We performed a quantitative characterization of binocular disparity-tuning functions in the ventral (object-processing) pathway of the macaque visual cortex. We measured responses of 452 area V4 neurons to stimuli with disparities ranging from -1.0 to +1.0 degrees. Asymmetric Gaussian functions fit the raw data best (median R = 0.90), capturing both the modal components (local peaks in the -1.0 to +1.0 degrees range) and the monotonic components (linear or sigmoidal dependency on disparity) of the tuning patterns. Values derived from the asymmetric Gaussian fits were used to characterize neurons on a modal x monotonic tuning domain. Points along the modal tuning axis correspond to classic tuned excitatory and inhibitory patterns; points along the monotonic axis correspond to classic near and far patterns. The distribution on this domain was continuous, with the majority of neurons exhibiting a mixed modal/monotonic tuning pattern. The distribution in the modal dimension was shifted toward excitatory patterns, consistent with previous results in other areas. The distribution in the monotonic dimension was shifted toward tuning for crossed disparities (corresponding to stimuli nearer than the fixation plane). This could reflect a perceptual emphasis on objects or object parts closer to the observer. We also found that disparity-tuning strength was positively correlated with orientation-tuning strength and color-tuning strength, and negatively correlated with receptive field eccentricity.

Animals↗

Visual perception of surface wrinkles.

To study the relationship between visual perception of magnitude of wrinkles and geometrical parameters of surfaces, four potentially relevant parameters of the surface profile were considered: the variance (sigma2), the cutting frequency (Fc), the effective disparity curvature (Dce) of the wrinkled surface over the eyeball distance of the observer, and the frequency component of the disparity curvature (Dcf). Analysis of garment seams with varying amount of pucker showed that, while the logarithm for each of these four parameters has a strong linear relationship with the visually perceived magnitude of wrinkles, following the Fechner Law, the effective disparity curvature (Dce) and the frequency component of the disparity curvature (Dcf) with visual perception appeared stronger. This modeling may be an objective method for measuring magnitude of surface wrinkles.

Clothing↗

Asymmetrical adaptation of human saccades to anisometropic spectacles.

We report the extent to which effective asymmetrical saccadic adaptation was achieved by a myopic subject, who was exposed to "long-term" adaptation as he wore anisometropic corrective spectacles for about 40 years and also the extent of "short-term" adaptation in this subject and two other subjects, who initially made conjugate saccades, when they wore newly fitted anisometropic spectacles for about 8 hr. Two-dimensional binocular eye positions were measured with an accurate and precise revolving magnetic field-sensor coil technique. We found that long-term adaptation of vertical saccades was virtually perfect (almost 100% of the asymmetry introduced by the spectacles was corrected). Long-term adaptation of horizontal saccades was less complete and increased with target separation from about 40% for saccadic amplitudes of 5 degrees to about 75% for amplitudes of 60 degrees. Short-term adaptation of vertical saccades was virtually complete (100%) in one newly fitted subject and only partially complete (40%) in the other two subjects. The persistence of the adaptive asymmetry of saccades during monocular viewing showed that adaptation derived from plasticity in the programming of saccades and not from modification of vergence responses. Without the anisometropic spectacles, 30 min of self-paced, one per second changes in binocular fixation between two targets, which required a version change of 45 degrees in combination with a vergence change of 11 degrees, did not induce any asymmetrical adaptation. This result shows that a specific repeated association of version and vergence eye movements was not sufficient to induce asymmetrical adaptation, leading us to suggest that the transient fixation disparities at saccade-offset might be the necessary stimulus for the asymmetrical saccadic adaptation we observed.

Adaptation, Physiological↗

Stereoscopic (cyclopean) motion sensing.

This paper reviews literature on the motion processing of dynamic change in binocular disparity, called stereoscopic (cyclopean) motion. Studies investigating the visual processing of stereoscopic motion in the Z-axis, stereoscopic motion in the X/Y plane, and cyclopean motion are discussed. It is concluded that stereoscopic motion is processed by a motion-sensing system composed of special-purpose mechanisms that function like low-level motion sensors. For animals with binocular vision, low-level motion processing may involve, at least in part, stereoscopic processing.

Animals↗

Clinical implications of vergence adaptation.

Placement of a prism in front of an eye results in a change in the tonic position of the eyes, a shift in the forced fixation disparity curve, and a shift in fusional amplitudes. These changes remain in effect as long as motor fusion is maintained. Elimination of fusion by occlusion or by removal of the prism results in a slow movement of the eyes back to the preprism position. This phenomenon, known as prism adaptation or slow fusional vergence, has important clinical implications in maintaining binocular vision with anisometropic prescriptions, age-related physiological changes in the positions of the eyes, blinking, high phorias, etc. Vergence adaptation is useful in explaining previous discrepancies between alternate and unilateral cover test, pre- and postorthoptic ACA ratios, stimulus and response ACA ratios, changes in phorias after orthoptics, and the observation of patients "eating up prism." Vergence adaptation anomalies have been implicated in causing asthenopia. Adaptation has been shown to change after orthoptic therapy. This paper reviews the clinical findings associated with vergence adaptation.

Adaptation, Ocular↗

Effects of diazepam on the latency of saccades for luminance and binocular disparity defined stimuli.

Saccadic latency is composed of separate sensory and motor processing delays. Therefore, any alteration in the sensory processing should effect the saccadic latency. Because the highest density of benzodiazepine (Bz) binding sites is located in cerebral cortex, sensory processing of stimuli in this cortical area is expected to be substantially effected by administration of Bzs. It is well known that sensory processing of binocular disparity occurs in the cerebral cortical areas and therefore the latency of saccades to stimuli defined by binocular disparity should be substantially affected by Bz intake. In this study, we tested this prediction by comparing the latency of saccadic eye movements for binocular disparity defined stimuli (stereo stimuli) with those for luminance contrast defined stimuli (luminance stimuli), after diazepam or placebo. Eye movements were mainly recorded by use of the magnetic search coil technique, and the study was performed in a randomized, double-blind way. Although diazepam prolonged the latency of saccades for stereo and luminance stimuli, the percentage increases in saccadic latency for the stereo stimuli were significantly larger than those for the luminance stimuli. Saccadic peak velocity, and saccadic amplitude, also significantly decreased after diazepam under conditions of stereo and luminance stimuli. However, there was no significant difference for either saccadic peak velocity or amplitude between the two types of target. The results suggest that the latency of saccades to binocular disparity defined random-dot stimuli could more sensitively reflect the pharmacodynamic effects of Bzs on the cerebral cortex.

Adult↗

Disparity averaging across spatial scales.

To determine whether disparity averaging occurs across spatial scales, a series of depth matching experiments was performed using stimuli composed of the sum of two cosine gratings of different spatial frequency and retinal disparity. Although there were large individual differences in the data, averaging was observed when the relative frequency of the cosines were separated by 3.5 octaves or less and when the relative orientation was less than 30 deg. Beyond these limits, averaging never occurred and the stimulus components were perceived transparently in depth. Furthermore, as the relative contrast of the gratings was varied, perceived depth varied smoothly in the direction of the higher contrast component. This dependence on contrast can be accounted for by a multi-channel model in which separate disparity estimates are generated on each spatial scale and then combined to determine the overall perceived depth of the stimulus.

Contrast Sensitivity↗

Asymmetrical effect of crossed and uncrossed disparity on stereoscopic capture.

When a real or subjective contour is superimposed on a repetitive texture or 'wallpaper pattern', the apparent depth of the elements of the wallpaper pattern may be influenced by the contour. When the contour has crossed disparity, the elements inside the contour are seen floating in the plane of the contour. This is called 'stereoscopic capture'. On the other hand, when the contour has uncrossed disparity a different, somewhat unstable, percept is seen. The wallpaper elements are either seen to form a transparent surface floating in front of the contour, or all of the elements inside and outside of the contour are seen to lie in the uncrossed plane of the inducing contour. We suggest that the asymmetry between crossed and uncrossed stereo capture is a by-product of the different roles played by crossed and uncrossed disparity in stereoscopic surface construction: specifically, crossed and, perhaps, zero disparity spreads one-directionally into a figure from a contour whereas uncrossed disparity spreads out from a figure in all directions. These points are illustrated with a series of demonstrations.

Adult↗

Influence of proximal, accommodative and disparity stimuli upon the vergence system.

The most important cues to the normal vergence response are retinal disparity, accommodative effort and perceived distance (proximal cue). In the past, proximal cues have been thought to contribute little to the total vergence response but more recent studies have suggested that they play an important role. The relative contributions of the proximal, accommodative and disparity cues to the vergence response were assessed by measuring the effect upon the vergence system when each of these cues were altered. The effect upon the vergence system was measured by the change in 'phoria, the change of fixation disparity and the amount of prism adaptation after 210 s of binocular viewing. The results indicate that the greatest effect of cue disharmony occurred when the proximal and disparity cues were altered. A finding which signifies the importance of the proximal cue to the overall vergence response.

Accommodation, Ocular↗

Response to motion in extrastriate area MSTl: disparity sensitivity.

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 facilitate such segmentation would be sensitivity to binocular disparity in the center and surround regions of the receptive fields of these neurons. We therefore investigated the sensitivity of these MSTl neurons to disparity ranging from three degrees crossed disparity (near) to three degrees uncrossed disparity (far) applied to both the center and the surround regions. Many neurons showed clear disparity sensitivity to stimulus motion in the center of the receptive field. About (1)/(3) of 104 neurons had a clear peak in their response, whereas another (1)/(3) had broader tuning. Monocular stimulation abolished the tuning. The prevalence of cells broadly tuned to near and far disparity and the reversal of preferred directions at different disparities observed in MSTd were not found in MSTl. A stationary surround at zero disparity simply modulated up or down the response to moving stimuli at different disparities in the receptive field (RF) center but did not alter the disparity tuning curve. When the RF center motion was held at zero disparity and the disparity of the stationary surround was varied, some surround disparities produced greater modulation of MSTl neuron response than did others. Some neurons with different disparity preferences in center and surround responded best to the relative disparity differences between center and surround, whereas others were related to the absolute difference between center and surround. The combination of modulatory surrounds and the sensitivity to relative difference between center and surround disparity make these MSTl neurons particularly well suited for the segmentation of a moving object from the background.

Analysis of Variance↗

Hysteresis, cooperativity, and depth averaging in dynamic random-dot stereograms.

Experiments were performed to assess the response of the human visual system to dynamic random-dot patterns composed of disparity mixtures. In Experiment 1, the perceived depth and relative stability of two patterns were compared; one pattern depicted two transparent layers of dots, and the other depicted a volume of dots. Two effects were found: (1) the volume pattern exhibited a large degree of disparity averaging; and (2) asymmetries were observed in the relative stability of these two patterns. Experiment 2 was designed to determine whether these findings could be attributed to spatially localized processes occurring at the location of disparity discontinuities. This was accomplished by introducing unpaired noise points localized either along the disparity discontinuities or in the center of the layered and volume patterns. The amount of depth averaging and the direction of the asymmetry did not appear to depend on processes localized along the disparity discontinuities. Results of these experiments, taken in conjunction with those of previous studies, suggest that hysteresis is independent of cooperative persistence mechanisms.

Adult↗

Global speed averaging is tuned for binocular disparity.

The extent to which local speeds at different depths are averaged to determine global speed was determined using a version of the Global Dot Motion (GDM) stimulus. Judgments of the apparent speed of fast moving dots (4.05-10.53 deg/s) in the presence of slow moving dots (4.05 deg/s) were measured using GDM stimuli which simulated radially expanding motion, and which confined slow and fast speed dots exclusively to alternating wedge shaped sectors. The presence of slow moving dots in the stimulus reduced the apparent speed of high-speed dots in a manner consistent with speed averaging. However with increases in depth, produced by a difference in binocular disparity between dots in alternating sectors, speed averaging became less effective, and the relationship between speed and disparity resembled a tuning function. We discuss our results in light of research that clarifies the functional properties of global motion mechanisms in the primate cortex.

Animals↗