Depth perception of the Syrian hamster as a function of age and photic condition of rearing.
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Age Factors↗
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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↗
Depth perception in moving line patterns.
By means of a computer system, the two-dimensional projections of a three-dimensional random wire figure, rotated clockwise (CW) or counterclockwise (CCW) about the vertical axis, were produced and displayed on a CRT. Generally the stimulus display appeared as an object rotating in depth, changing direction of movement frequently from clockwise rotation to counterclockwise, and vice versa. In the experiment, the three subjects observed the displays of three different types of projection, two polar projections and a parallel one. They were instructed to judge the direction of the seen motion and asked to report it using the button-switches. Both duration of the rotation perceived in either direction and frequency of the apparent reversals between those two were measured from the output sheets of a pen-recorder. The results showed the effects of the type of projection. (1) The veridical motions were perceived more continuously and durably in the polar projections than in the parallel one, (2) the opposite relation was found with the nonveridical motions, and (3) the reversals of moving direction were seen more frequently in the parallel projection than in the polar ones.
Adult↗
The role of eye accommodation in the depth perception of common toads.
Distance estimation in prey catching was as exact in monocular toads (Bufo bufo (L.)) as in binocular ones. Application of Atropine or Miotic had no significant effect on binocular animals, whereas in monocular toads it made accurate distance estimation impossible. The accommodative state of the eye is decisive for depth estimation of monocular, but not of binocular toads.
Accommodation, Ocular↗
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↗
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↗
Traffic signals and depth perception.
Automobiles approaching red traffic signals at night appear to go beyond them when viewed from some distance to the rear. The phenomenon is doubly illusory because the higher of two objects has been presumed to appear more distant. The illusion is probably limited to small visual angles (about 2 degrees).
Automobile Driving↗
Depth perception and evoked brain activity: the influence of horizontal disparity and visual field location.
The perception of dynamic random-dot stereograms (RDS) depends on the physiological fusion of horizontally disparate binocular visual input. Thus, the use of RDS offers the possibility to study selectively cortical processing of visual information in man. We investigated the influence of horizontal disparity on the scalp topography of RDS evoked brain activity in 33 healthy subjects. Stereoscopic checkerboard patterns were presented in the center or lateralized in the left or right visual field with horizontal disparities changing at temporal frequencies of six or eight depth reversals/s using different disparity values ranging from 3.5 to 28 min of arc. In 11 subjects evoked potential fields were recorded from 16 electrodes, and 21 subjects participated in 30-channel recordings with electrodes located over the parietal and occipital brain areas. Stimulation frequency-related brain activity was obtained with all disparity values; however, with large or small disparities the potential field strength decreased significantly while largest responses were obtained with intermediate disparities. Significant differences were observed in RDS evoked brain activity when central and lateralized stimulus locations were compared. With lateral stimuli (extending from the fovea to 17.1-deg eccentricity) maximal amplitudes were obtained at larger disparities than with central stimuli. In addition there were pronounced differences between brain activity evoked with stimuli presented in the left or right visual field; however, there were very similar evoked potential signals recorded from electrodes located over the left and right hemispheres. Our findings indicate that the processing of disparity information with lateralized stimuli is different from the processing in the center of the visual field. In addition, lateralized stimulation yields a significant disparity tuning mainly with stereoscopic targets occurring to the right from the fixation point (but not with stimuli to the left) suggesting a functional difference between the visual half-fields.
Adult↗
Stereoscopic depth perception and vertical disparity: neural mechanisms.
The additivity assumption relates to the various stereo-disparity components in the vertical and horizontal meridians, each of which is assumed to be independent of the other, with the total disparity in each dimension being the linear sum of the separate components. Information about the position of the eyes provided by the corollary discharge leads to compensatory changes in the lateral geniculate nuclei whereby the angle of gaze disparity component at retinal level is offset by equal and opposite changes at geniculate level. These geniculate changes concern only eye position. Changes in the retinal images such as those produced by lenses (i.e. induced effect) are passed on to the cortex without modification at the geniculate level. Discrimination of the local depth disparity component can be achieved by subtracting the local vertical eccentricity component from the total horizontal disparity.
Depth Perception↗
Modelling human depth perception in binocular vision: obtaining the horizontal disparity map.
The paper presents a computer application developed as a tool for implementing, developing, and testing computational models for stereopsis. Two models for solving the correspondence problem and computing the stereo disparity map have been implemented. One of them is biologically inspired (it models the behaviour of simple and complex cells from the striate cortex) and the paper details the results obtained on random-dot stereograms and on pairs of real images.
Algorithms↗
A computational model of binocular depth perception.
We point out that the horizontal disparities between a pair of retinal images are inadequate for computing the three-dimensional structure of a scene unless supplemented by independent information about the distance and direction of the fixation point. We suggest that this supplementary information is derived not from non-visual sources, but from the vertical disparities of a few non-meridional image points. This hypothesis is shown to account quantitatively for Ogle's induced effect--the marked distortion of a scene by a vertically magnifying lens placed in front of one eye.
Depth Perception↗
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↗
Frequency of fusion and of loss of fusion, and binocular depth perception with alternating stimulus presentation.
Stereoscopic vision was investigated with an experimental design allowing dichoptic stimulus presentation at different frequencies of image alternation. For twenty subjects the frequency of binocular fusion and the frequency of loss of fusion to one stereoscopic image was measured as a function of the convergence angle. In thirteen subjects no dependence of the fusion frequency was found, while seven subjects showed a marked increase of the fusion frequency with increasing angle of convergence. In all cases the frequency of fusion was higher than the frequency of loss of fusion. Both frequencies, however, are lower than the flicker fusion frequency. Under conditions where no monocular cues and no references for stereoptic depth comparisons were presented, the apparent distance of the image from the observer could not be assessed, but perception of relative motion in depth was possible. All subjects assessed the direction of motion accurately down to changes of the convergence angle of 0.2 deg s-1.
Adolescent↗
Sensory modalities in depth perception by golden hamsters.
Golden hamsters are able to detect differences in the height of a platform from which they jump, as measured by their increasing latencies prior to jumping from increased elevations. This ability is very effective when optical information is available, but it is also present when hamsters jump in total darkness. A second experiment shows that, when hamsters are placed on a real physical cliff, they preferentially use tactile information over visual information to guide their choice of the side from which to descend. In a nonvisual setting, tactile stimulation is used in conjunction with other types of cues. Evidence is provided to suggest that these cues are of an acoustical nature.
Animals↗
A possible neurophysiological basis for depth perception in frogs: existence of a horopter surface.
In frogs, multi-unit receptive fields (MURF) of rostral binocular tectal points (BTP) show a crossed disparity when mapped at a distance equal to the perimeter radius (i.e., 33 cm). The shape of the spatial surface where MURF of all BTP are in-register is investigated in two planes: (a) in the longitudinal plane, the locus of superimposition is a circumference passing through both eyes; (b) in the vertical plane, it corresponds to a straight line tilted towards the animal's head. This surface can be defined as the frog's horopter surface since it represents the spatial locus where objects can simultaneously stimulate corresponding retinal areas. Behavioural and electrophysiological correlations are discussed.
Animals↗
Modelling biological depth perception in binocular vision: the local disparity estimation.
This paper presents an approach to solving the correspondence problem in binocular vision and to computing the local horizontal disparity map using a biologically inspired algorithm. A computer application was developed as a tool for implementing, developing, and testing computational models for stereopsis, and also as a framework for integrating the disparity map with other perspective clues. Two models for stereopsis have been implemented. One of them is biologically inspired (it models the behaviour of simple and complex cells from the striate cortex) and the other is the 'classical' model of David Marr and Tomaso Poggio, implemented in order to have a comparison term for the simulation results. The paper details the results obtained on random-dot stereograms and on pairs of real images.
Algorithms↗
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↗
Stereoscopic depth perception at high velocities.
The view of the world from different perspectives provided by the two eyes is used by the human visual system to compute the relative distances and solid shapes of objects. However, the traditional theory of binocular disparity takes little account of the fact that a moving target will stimulate many different sets of disparate points in the two eyes with a range of temporal delays. Here we show that stereoacuity for periodic grating is not degraded by velocities of up to 640 degrees s-1 provided that they do not move at a greater rate than 30 cycles s-1. The minimum detectable spatial phase difference between the eyes was equivalent to a spatial phase difference of about 5 degrees and an interocular temporal delay as small as 450 microseconds. We suggest that stereopsis for moving targets is accomplished by neurons having a spatial-temporal phase shift in their receptive fields between the eyes.
Depth Perception↗