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PubMed2001

Hierarchical processing of horizontal disparity information in the visual forebrain of behaving owls.

According to their restricted receptive fields and input-filter characteristics, disparity-sensitive neurons at early processing levels of the visual system perform rather ambiguous computations; they respond vigorously to disparity in false-matched images and show multiple response peaks in their disparity-tuning profiles. On the other hand, the perception of depth from binocular disparity is reliable, thus raising the question as to where and how in the brain additional processing is accomplished leading toward behaviorally relevant disparity detection. To address this issue, tuning data during stimulation with correlated and anticorrelated random-dot stereograms (a-RDS) were obtained from 52 disparity-sensitive visual Wulst neurons in three behaving owls. From the disparity-tuning curves, several quantitative measures were derived that allowed to determine the response ambiguity of a cell. A systematic decline of response ambiguities with increasing response latencies was observed. An increase in response latencies of neurons was correlated with a decrease of the strength of responses to a-RDS. Declining responses to a-RDS are expected for global detectors, because an owl was not able to discriminate depth in psychophysical tests with a-RDS. In addition, suppression of response side peaks was increased and disparity tuning was enhanced with growing response latencies. These results suggest a functional hierarchy of disparity processing in the owl's forebrain, leading from spatial filters to more global disparity detectors that may be able to solve the correspondence problem. Nonlinear threshold operations and inhibition are proposed as candidate mechanisms to resolve coding ambiguities.

Action Potentials↗
PubMed2001

[Design of multi-channel EEG collection system for stereoscopic VEP and study of the VEP evoked by binocular disparity].

A multi-channel EEG collection system has been constructed for visual evoked potentials (VEP) studies, using IBM compatible PC and clinical EEG amplifier. The collection system not only is suitable for investigative and clinical use, but also works perfectly in the EEG collection and signal processing of stereoscopic VEP. The characters of the depth related VEP evoked by binocular disparity were identified after analysing and comparing the VEP superposition results. The partial results of the VEP extraction are in accord with the previous studies. The system serves as a helpful tool in studies of stereoscopic cognition and brain function.

Adult↗
PubMed2000

Asymmetry in 3-D perceptual organization: ground-like surface superior to ceiling-like surface.

Attneave (1954) and Barlow (1961) proposed that the visual system might increase efficiency of representation by preferentially encoding spatiotemporally redundant patterns of the external world. The present experiments tested the application of this principle to three-dimensional (3-D) perceptual organization, capitalizing on the ecological constraint that human observers must frequently interact with objects arranged on the ground or on a surface parallel to it (Gibson, 1950). Observers performed a task that required them to perceptually segregate and search multiple items distributed in depth and embedded within a larger, 3-D array of distractors. Stimulus displays were organized to globally recede top-away in depth, as if attached to an underlying ground-like surface, or bottom-away, as if attached to an overhanging ceiling-like surface; ground-like and ceiling-like displays differed only in the direction of disparity gradient within the displays. Primary findings revealed superior performance with ground-like displays, suggesting that spatially and stereoscopically distributed items are more easily organized to represent an ecologically representative pattern, even when no inherent physical regularities favor that pattern.

Adult↗
PubMed2000

What limits the contribution of second-order motion to the perception of surface shape?

Both motion and stereopsis can be derived from contrast as well as luminance defined stimuli. It is currently assumed that these two different sources of information about objects feed into one common stage. Thus it would not be expected that their role in visual perception would be different. Here we show that although motion can be carried by contrast-defined elements, such motion is not used to define three-dimensional (3D) surfaces. A similar effect has been reported in stereopsis; although such contrast-defined elements can give signed disparity signals they nevertheless do not contribute to the percept of shape. We show that the reason for this lies in the inability of the second order signals to cohere or bind across space/spatial scales rather than a characteristic of the elementary motion signals per se.

Contrast Sensitivity↗
PubMed2001

Receptive field organization of disparity-sensitive cells in Macaque medial superior temporal cortex.

Binocular disparities are crucial for building an accurate three-dimensional representation of the peripersonal environment in a viewer-centred frame of reference. Previous studies have shown that visual cells of the medial superior temporal cortex (MST) have large receptive fields and that they are sensitive to disparities present in large surfaces. By using a reverse cross-correlation technique in this study we tested 175 disparity-sensitive units recorded from MST in the awake Macaca mulatta monkey to determine if these large receptive fields are homogeneous in terms of disparity sensitivity. We found that the receptive fields of 50 cells (50 out of 175, 29%) showed subregions with specific disparity sensitivity. These subregions presented eccentricities from 0.8 to 22.3 degrees and their sizes varied from 1.6 to 15.3 degrees 2. This particular receptive field organization represents a suitable mechanism for encoding the location of small objects within our peripersonal space.

Action Potentials↗
PubMed1996

Perceptual learning of stereoacuity.

It has often been noted that with repeated exposure to random-dot stereograms the time required to perceived depth decreases. Further, with extensive practice, stereoacuity thresholds have been shown to decrease. For both types of learning some researchers have reported specificity of the improvements to retinal location, and have thus suggested that the learning may be localised at early levels of visual processing, such as in primary visual cortex. However, these studies have not adequately ruled out the possibility that the specificity shown may be due to the operation of selective-spatial-attention mechanisms. In the present study this possibility was examined by training observers to judge the relative depth of a pair of stereograms presented equally often in two spatial locations, but stimuli were only presented with one direction of disparity (ie crossed or uncrossed) in any one location. Results indicated that, as expected, observers' judgements improved with practice. However, this improvement transferred completely to stimuli presented with the other direction of disparity in each location. Thus, it is argued that previous findings of retinal-location-specific improvements in stereoacuity may well be due to selective-spatial-attention mechanisms, rather than to learning localised at an early level of visual processing.

Adult↗
PubMed1992

Vertical vergence adaptation for normal and hyperphoric patients.

This paper discusses the use of vertical fixation disparity (VFD) measurements to determine a patient's ability to adapt to vertical prism. Vertical vergence adaptation for orthophoric patients, hyperphoric patients, and patients with vertical deviations associated with superior oblique paresis is reported. The effect of orthoptic training on the ability to adapt to vertical prism is also reported.

Adaptation, Ocular↗
PubMed2006

How behavioral constraints may determine optimal sensory representations.

The sensory-triggered activity of a neuron is typically characterized in terms of a tuning curve, which describes the neuron's average response as a function of a parameter that characterizes a physical stimulus. What determines the shapes of tuning curves in a neuronal population? Previous theoretical studies and related experiments suggest that many response characteristics of sensory neurons are optimal for encoding stimulus-related information. This notion, however, does not explain the two general types of tuning profiles that are commonly observed: unimodal and monotonic. Here I quantify the efficacy of a set of tuning curves according to the possible downstream motor responses that can be constructed from them. Curves that are optimal in this sense may have monotonic or nonmonotonic profiles, where the proportion of monotonic curves and the optimal tuning-curve width depend on the general properties of the target downstream functions. This dependence explains intriguing features of visual cells that are sensitive to binocular disparity and of neurons tuned to echo delay in bats. The numerical results suggest that optimal sensory tuning curves are shaped not only by stimulus statistics and signal-to-noise properties but also according to their impact on downstream neural circuits and, ultimately, on behavior.

Animals↗
PubMed2003

Disparity-based coding of three-dimensional surface orientation by macaque middle temporal neurons.

Gradients of binocular disparity across the visual field provide a potent cue to the three-dimensional (3-D) orientation of surfaces in a scene. Neurons selective for 3-D surface orientation defined by disparity gradients have recently been described in parietal cortex, but little is known about where and how this selectivity arises within the visual pathways. Because the middle temporal area (MT) has previously been implicated in depth perception, we tested whether MT neurons could signal the 3-D orientation (as parameterized by tilt and slant) of planar surfaces that were depicted by random-dot stereograms containing a linear gradient of horizontal disparities. We find that many MT neurons are tuned for 3-D surface orientation, and that tilt and slant generally have independent effects on MT responses. This separable coding of tilt and slant is reminiscent of the joint coding of variables in other areas (e.g., orientation and spatial frequency in V1). We show that tilt tuning remains unchanged when all coherent motion is removed from the visual stimuli, indicating that tilt selectivity is not a byproduct of 3-D velocity coding. Moreover, tilt tuning is typically insensitive to changes in the mean disparity (depth) of gradient stimuli, indicating that tilt tuning cannot be explained by conventional tuning for frontoparallel disparities. Finally, we explore the receptive field mechanisms underlying selectivity for 3-D surface orientation, and we show that tilt tuning arises through heterogeneous disparity tuning within the receptive fields of MT neurons. Our findings show that MT neurons carry high-level signals about 3-D surface structure, in addition to coding retinal image velocities.

Animals↗
PubMed1989

The accommodative contribution to binocular vergence eye movements.

Forced vergence fixation disparity curves were generated for both with and without an accommodative stimulus (accommodative closed and open loop conditions respectively) for fifteen asymptomatic subjects. All subjects exhibited an exophoric shift in fixation disparity for the accommodative open loop condition at the forced convergence side of the curve. No corresponding bias was found at the forced divergence side of the curve. The findings are discussed in terms of the results of previous studies and the existing models of vergence eye movements.

Accommodation, Ocular↗
PubMed1993

An occluded contour becomes visible with reversal of disparity.

Suppose that there is a circle in front of a cross, the central part of which is occluded by the circle. One usually perceives these figures, as such, although the objective description of the stimulus pattern might be that there is a circle with four limbs attached to it. Here the occluded contours of the cross might be 'inferred.' Until now it has not been demonstrated clearly whether this 'inference' is based on higher cognitive processes or on perceptual processes. However, by manipulating binocular disparity so that the four limbs are seen in front of the circle, the occluded contours become visible, the color of the limbs spreads into the inside of the contours, and the color spreading surface appears transparent, suggesting that the 'inference' is on a perceptual basis. Interestingly, cornered subjective contours of the cross are observed.

Color Perception↗
PubMed2002

Population coding in cortical area MST.

Disparity steps applied to large patterns elicit vergence eye movements at ultrashort latencies. Disparity tuning curves, describing the dependence of the amplitude of the initial vergence responses on the amplitude of the disparity steps, resemble the derivative of a gaussian and indicate that appropriate servo-like behavior occurs only with small disparity steps (<1 degree). Lesion data from monkeys suggest that these vergence responses are mediated, at least in part, by neurons in the medial superior temporal area of the cerebral cortex, and we here review a recent study of the associated single unit activity in that area. Few medial superior temporal neurons have disparity tuning curves whose shapes resemble the tuning curve for vergence. Yet, when the disparity tuning curves for all of the disparity-sensitive cells recorded from a given monkey are summed together, they match the tuning curves for the vergence responses of that monkey very closely, even reproducing that animal's idiosyncracies. When all of the spike trains elicited by a given disparity step are summed together to give an average discharge profile for the whole population of recorded cells, many are noisy, but others that are less so match the temporal profile of the motor response, vergence velocity, quite well. We conclude that the discharges of the disparity-sensitive cells in the medial superior temporal area each represent only a very limited aspect of the sensory stimulus (and/or associated motor response?), but when pooled together, they provide a complete description of the vergence velocity motor response: population coding.

Animals↗
PubMed2005

Properties of pupillary responses to dynamic random-dot stereograms.

Pupillary response can be elicited by a number of visual stimuli. In the present experiments, the pupillary responses to stereo gratings with various spatial frequencies and disparity amplitudes were measured. The spatial frequency was from 0.1 to 1.2 cycles per degree (cpd), and the disparity amplitude was from 4 to 24 min arc. The results showed that pupillary responses can be elicited by all these stereo gratings except when either the spatial frequency or disparity amplitude was reduced to zero. When the disparity amplitude was fixed to 8 min arc, the pupillary response amplitude increased with increasing spatial frequency, eventually reaching a plateau. While the spatial frequency was fixed to 0.3 cpd, the pupillary response amplitude continued to increase within the range of disparity amplitude. This provides a different approach to demonstrate that these pupillary responses were induced by stereo information. In addition, the stereo pupillary responses may be further developed as an objective method to study stereopsis. Finally, plausible underlying mechanisms of the stereo pupillary response are discussed.

Depth Perception↗
PubMed2002

Conditions under which stereopsis and motion perception are blind.

We describe modified random-dot stereograms in which the corresponding elements differ from non-corresponding elements in colour, size, and luminance. Despite these visible differences between the elements, depth perception collapses when the spatially integrated luminous flux is similar for the corresponding and non-corresponding elements. Our results suggest that a low-pass spatial filter precedes the mechanism that recognises disparity. A similar phenomenon is observed for the perception of coherent motion in random-dot kinematograms. Our modified stereograms and kinematograms may find other uses when experimenters wish to study the contribution of colour to visual processes and require a method of eliminating edge artifacts.

Adult↗
PubMed2000

Binocular disparity can explain the orientation of ocular dominance stripes in primate primary visual area (V1).

In the primate primary visual area (V1), the ocular dominance pattern consists of alternating monocular stripes. Stripe orientation follows systematic trends preserved across several species. I propose that these trends result from minimizing the length of intra-cortical wiring needed to recombine information from the two eyes in order to achieve the perception of depth. I argue that the stripe orientation at any point of V1 should follow the direction of binocular disparity in the corresponding point of the visual field. The optimal pattern of stripes determined from this argument agrees with the ocular dominance pattern of macaque and Cebus monkeys. This theory predicts that for any point in the visual field the limits of depth perception are greatest in the direction along the ocular dominance stripes at that point.

Animals↗
PubMed1988

Dynamic stereoacuity: a comparison of electrophysiological and psychophysical responses in normal and stereoblind observers.

We compared stereoscopic thresholds determined psychophysically and by using visually evoked potentials in normal adult and stereoblind subjects. For normal observers there was a strong linear relationship between visual evoked potential amplitude and disparity (r = 0.86 on average). However, stereoblind observers' responses showed no relationship to disparity (r = 0.18 on average). For normal observers, log visual evoked potential stereo thresholds determined by an extrapolation procedure were on average within 0.17 octaves of the psychophysically determined log thresholds. They did not differ significantly from psychophysical thresholds, and they correlated significantly with behavioral thresholds (r = 0.86).

Adult↗
PubMed2006

Subjective appearance of ambiguous structure-from-motion can be driven by objective switches of a separate less ambiguous context.

Two ambiguous transparent structure-from-motion (SFM) stimuli often appear to co-rotate. Grossmann & Dobbins (2003) reported breakdown of such perceptual coupling when one stimulus was made unambiguous (by rendering it opaque), leading them to propose that coupling depends generally on differential stimulus ambiguity. In contrast, we demonstrate robust stimulus-driven coupling even when one SFM stimulus is relatively disambiguated, by using relative-luminance and/or binocular-disparity cues. Such context stimuli could induce stimulus-driven coupling by disambiguating the transparent stimulus, though critically only when the context was clearly non-opaque and coaxial with the ambiguous stimulus. This demonstrates long-range information-sharing between separate stimulus representations, subject to specific constraints.

Adult↗
PubMed2001

[Roles of posterior parietal cortex in stereopsis: characteristics of responses of axis-orientation-selective neurons in monkey caudal intraparietal area].

Patients with parietal lesions may fail to adjust the orientation of their hand to that of a target object, or may make errors in judging the orientation of a bar. This suggests that the parietal cortex has a function in the discrimination of the orientation of objects. In this study we investigated the responses of axis-orientation-selective neurons in caudal intraparietal (CIP) area to stereoscopic stimuli. Among the characteristics we investigated responses to the length and thickness of objects, sensitivity to binocular disparity, and position invariance in depth. Computer generated stereoscopic stimuli were presented to the monkey on a 70 inch screen. Most of the neurons responded better to long or narrow stimuli. All neurons which were orientation selective only in the frontal plane were not disparity sensitive. Most of the neurons which were orientation selective in the sagittal or horizontal plane were sensitive for binocular disparity. The majority of these neurons had wide receptive fields and their responses were position-invariant. These results suggest that the axis-orientation-selective neurons in CIP area encode the orientation of the longitudinal axis of objects in 3-dimensional space.

Animals↗