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PubMed1988

Dynamic occlusion and motion parallax in depth perception.

Random-dot techniques were used to examine the interactions between the depth cues of dynamic occlusion and motion parallax in the perception of three-dimensional (3-D) structures, in two different situations: (a) when an observer moved laterally with respect to a rigid 3-D structure, and (b) when surfaces at different distances moved with respect to a stationary observer. In condition (a), the extent of accretion/deletion (dynamic occlusion) and the amount of relative motion (motion parallax) were both linked to the motion of the observer. When the two cues specified opposite, and therefore contradictory, depth orders, the perceived order in depth of the simulated surfaces was dependent on the magnitude of the depth separation. For small depth separations, motion parallax determined the perceived order, whereas for large separations it was determined by dynamic occlusion. In condition (b), where the motion parallax cues for depth order were inherently ambiguous, depth order was determined principally by the unambiguous occlusion information.

Attention↗
PubMed1975

Depth perception in the rat (Rattus Norvegicus): prepotency of three-dimensional over two-dimensional surfaces.

The descent behavior to two- and three-dimensional surfaces in a depth situation was measured and compared for 45-50 days-old hooded rats. When depth differences between surfaces were controlled, significantly more descents were made to three-dimensional than to the two-dimensional surface. The results suggest that a three-dimensional surface--more representative of an animal's natural terrain--provides a more informative environment for motion parallax than does a two-dimensional one.

Animals↗
PubMed1986

Binocular depth perception in the pigeon.

By means of a discrete-trial simultaneous discrimination procedure, pigeons were trained to respond differentially to visual arrays that were identical except that one of them contained a circle displaced in depth when viewed stereoscopically. Performance was severely disrupted when one eye was occluded. The monocular deficit was peculiar to the depth task, inasmuch as no such decrement was seen on a pattern discrimination. The results imply that presence of the displaced circle was discriminated on the basis of a binocular cue. It was also found that pigeons could discriminate the direction of the displacement. Discrimination of depth was independent of the global form and still occurred when elements of the array were randomly displaced in depth. Performance was not disrupted when the absolute convergence angle of the depth stimulus was changed. The cue that consistently accounted for the behavior seen was the detection of the relative angles of convergence--that is, the retinal disparity of the two planes in depth. Thus, despite the lateral position of the eyes of the pigeon, a small binocular field mediates the binocular discrimination of near objects in depth.

Animals↗
PubMed1979

Motion parallax as an independent cue for depth perception.

The perspective transformations of the retinal image, produced by either the movement of an observer or the movement of objects in the visual world, were found to produce a reliable, consistent, and unambiguous impression of relative depth in the absence of all other cues to depth and distance. The stimulus displays consisted of computer-generated random-dot patterns that could be transformed by each movement of the observer or the display oscilloscope to simulate the relative movement information produced by a three-dimensional surface. Using a stereoscopic matching task, the second experiment showed that the perceived depth from parallax transformations is in close agreement with the degree of relative image displacement, as well as producing a compelling impression of three-dimensionality not unlike that found with random-dot stereograms.

Cues↗
PubMed1976

Depth perception after infant and adult visual neocortical lesions in light- and dark-reared rats.

In 2 experiments the behavior of light- and dark-reared infant- and adult-operated striate rats were compared at 20-160 days of age on a visual cliff apparatus in which the depth of the deep side could be varied. Differential depth thresholds revealed that depth discriminative ability did not develop normally following removal of the striate cortex in infancy. Further, infant-operates who were reared in darkness following their operations performed less well than their light-reared, infant-operated counterparts. The infant-operated animals, regardless of their postoperative rearing condition, performed significantly better than did adult-operated animals after comparable post-operative recovery periods and testing. The results are discussed in terms of further specification of the role played by age of operation and by the interaction between visual experience and age of operation.

Age Factors↗
PubMed1988

An occlusion-related mechanism of depth perception based on motion and interocular sequence.

Objects occlude other objects in natural scenes, and this occlusive relationship increases the spatio-temporal complexity of sensory inputs to the two eyes, especially when objects are moving. We ask whether the visual system can employ clever strategies which make use of real-world constraints on inputs to the eyes to determine the depth of objects. Employing psychophysical methods, we found that occlusion-related geometric rules, which constrain the relationship between the direction of motion and the order and asynchrony of eyes, are implemented at early stages of cortical visual processing.

Depth Perception↗
PubMed1989

Stereoscopic depth perception by static stereo-deficient observers in dynamic displays with constant and changing disparity.

The performance of 11 static stereo-deficient subjects and 11 static stereo-normal subjects was compared on two types of dynamic stereo displays--one where disparities were constant during motion and one where disparities changed continuously. Computer-generated displays simulating horizontal motion of figures at different depths or rotation of figures about a vertical axis were viewed through a Brewster stereoscope. About one-half of the subjects in our static stereo-deficient sample were able to make depth judgments on the basis of disparity in both types of dynamic displays. The clinical feature which appeared to distinguish those static stereo-deficient subjects who could use disparity information in dynamic displays from those who could not was early onset constant strabismus. These results indicate that a complete evaluation of stereo ability should include tests with dynamic displays, possibly including both constant and changing disparities.

Adult↗
PubMed1988

Deficits in stereoscopic depth perception by mildly mentally retarded adults.

The ability of mildly mentally retarded adults to perceive specific perceptual phenomena attendant to global stereopsis produced by random element stereograms was investigated. From the standpoint of computational vision, these phenomena are difficult to process, yet nonretarded persons perceive them effortlessly and without error. Retarded subjects in this study, however, exhibited large qualitative deficits not attributable to an absence of stereopsis or a failure to comprehend. These results suggest that the computational requirements of the stimuli exceeded resources and imply the presence of a substantial structural deficit in an automatic preattentive perceptual stage quite distant from the domain of cognition.

Adult↗
PubMed1979

Effect of meridional disparity on depth perception.

When a meridional-size lens is used to provide magnification in the horizonal meridan for one eye the resulting stereopsis distortion is readily accounted for in the terms of the binocular disparity caused by changed angular relations. When the same size lens is used to magnify the vertical meridian for one eye there is an opposite stereoscopic distortion for which is no ready geometric explanation. A perceptually induced mechanism operating in the vertical meridian has been suggested by Ogle. In the present experiment, apparatus was designed to introduce disparity of binocularly fused targets successively in each of several oblique meridians independent of the stereopsis measuring targets. Unlike the above-mentioned results obtained with size lenses, the induced stereoscopic distortion was in the same direction and of essentially the same magnitude for disparity in every meridian. It would follow that the perceptually induced mechanism is not exclusive to the vertical meridian.

Depth Perception↗
PubMed1987

Electrophysiological assessment of the human depth-perception threshold.

The cortical response to stereoscopic stimuli was measured as a function of disparity using visual evoked potentials (VEP). The stereoscopic stimulus consisted of a dynamic random-dot pattern that portrayed a three-dimensional horizontal grating. Disparity of the grating was variable between 0 and 18 arc min, step size being 4.22 arc s. Evoked responses were recorded using a "random-sequence sweep technique." The VEP amplitude increased approximately linearly with the logarithm of disparity and allowed an estimation of the stereo threshold by linear extrapolation. The evoked potential estimates of the stereo threshold of 16 subjects were compared to psychophysically obtained thresholds. Several threshold-estimation techniques are discussed. Evoked potential and psychophysical threshold estimates had the lowest discrepancy when the VEP amplitude was linearly extrapolated to the logarithmic disparity axis. The difference between the evoked potential estimate and the psychophysical threshold was less than 20% in 56% of all cases; 16 of 18 cases (89%) agreed within a factor of 2.

Depth Perception↗
PubMed1989

[Computer-assisted determination of parameters of depth perception: studies with the 3-rod device].

Psychophysical determination of the thresholds of stereoscopic vision takes about 20 min. During this procedure, you may have the feeling that the thresholds are shifting. To verify this phenomenon, the thresholds must be determined in a period shorter than 20 min, e.g., 4-6 min. This is one of the reasons we constructed a computerized machine to detect the stereoscopic thresholds. The heart of this device is a micrometric screw driven by a stepping motor that moves the central rod of the three-rod apparatus. This motor is controlled by a microcomputer with a basic program. A special program has been designed that functions in a manner similar to that of the Octopus perimeter and detects the thresholds with in a few steps. It is thus possible to reduce the detection time for one threshold dramatically. The first results with this device are not only very precise, but also demonstrate the minute values between stereoscopic thresholds. For an observation distance of 380 mm, we were able to calculate the disparation angles down to 3 s of arc. If a number of measurements are taken, the threshold fluctuations and physiological zero position can be calculated.

Depth Perception↗
PubMed1987

Chromatic imbalance due to commonly used red-green filters reduces accuracy of stereoscopic depth perception.

This study was designed to determine the effect on stereopsis of interocular retinal chromatic and illuminance imbalance in 30 subjects with normal binocularity. A Randot 3 Circle Stereotest, viewed through polarizing glasses only, was the control condition. In each of three additional conditions, illuminance and chromatic imbalances were created by commonly used red and green filters and neutral density filters combined with the polarizing filters. The effect of each of these experimental conditions on stereopsis was determined by comparing total stereo judgement errors on the Randot Circle Stereotest for each condition to the control condition. Total average flux through the filter combinations was held constant by adjusting the luminance level of light reflected from the target. The chromatic imbalance created by the red-green filters significantly increased the number of stereo judgment errors (37%, p less than 0.05). However, illuminance imbalance (0.2 log units) of the magnitude created by the red-green filters did not significantly increase the number of errors (2.9%, p less than 0.65). Finally, the combined illuminance and chromatic imbalance created by the red-green filters significantly increased the error frequency (46%, p less than 0.05). The chromatic imbalance caused by red-green glasses significantly degrades stereopsis, whereas the illuminance imbalance caused by these filters has no significant effect on stereopsis.

Adolescent↗