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PubMed1979

A test battery to assess intrasensory and intersensory development of young children.

The purpose of the study was to develop a battery of tests for use in evaluation of intra- and intersensory development of young children. A battery of 15 tests (4 visual, 4 auditory, 4 tactile-kinesthetic, and 3 intersensory) was administered to 109 normally developing 6- and 8-year-old and 32 slowly developing or learning disabled children. Interdependence of test items within each intrasensory and the intersensory category was determined; intercorrelations ranged from .00 to .78. Reliability estimates were also determined. Face validity was claimed for each item. The effects of age or developmental level on test performance were established. Based upon the interdependence of the tests, reliability estimates, and the capacity of the tests to discriminate among groups classified according to age or developmental level, a battery of 10 intra- and intersensory tests was proposed. The battery has 3 tests of visual perception-visual memory, dynamic depth perception, and size discrimination; 3 tests of auditory perception-auditory discrimination, auditory memory of related syllables, and auditory sequential memory of numbers; 2 tests of tactile-kinesthetic perception-tactile integration and movement awareness; and 2 tests of intersensory integration-auditory-tactile intergration and auditory-visual integration.

Age Factors↗
PubMed1976

Binocular-disparity-dependent upper-lower hemifield anisotropy and left-right hemifield isotropy as revealed by dynamic random-dot stereograms.

Dynamic random-dot stereograms devoid of all monocular depth cues were used to measure the limits of temporal and spatial resolution in the center of the visual field. The temporal durations for detecting a small, briefly presented test square of different binocular disparity than the surround varied as a function of its location and binocular disparity. The test squares presented in the upper hemifield were detectable at consistently shorter durations than those presented in the lower hemifield for a surround disparity which was uncrossed relative to the fixation marker. For crossed surround disparity this preference reversed, resulting in a superiority of the lower hemifield. The anisotropy diminished for zero surround disparity. No such anisotropy was found when left and right visual hemifields were compared. It was also shown that this upper-lower temporal anisotropy (and left-right isotropy) is paralleled by a similar disparity-dependent upper-lower anistropy (and left-right isotropy) in spatial resolution. Introduction of monocular clues into the stereograms tended to eliminate the anisotropies. This implies that the anisotropies reflect the spatiotemporal properties and distribution of binocular disparity detectors in the human cortex and result in a tilted surface that pivots around the horizontal midline in the space of binocular depth perception.

Depth Perception↗
PubMed1976

Selected visual abilities of college football players.

Relationships between visual abilities and athletic performance have been examined but reported findings are inconclusive and inconsistent. Data were collected from 40 volunteer college football players on horizontal peripheral vision, vertical peripheral vision, depth perception, and visual disembedding. No differences were found between varsity and junior varsity football players, indicating that relatively more successful players are not characterized by greater visual perception attributes.

Adult↗
PubMed1978

An inference upon the neural network finding binocular correspondence.

Previously, the authors proposed a model of neural network extracting binocular parallax (Hirai and Fukushima, 1975). It is a multilayered network whose final layers consist of neural elements corresponding to "binocular depth neurons" found in monkey's visual cortex. The binocular depth neuron is selectively sensitive to a binocular stimulus with a specific amount of binocular parallax and does not respond to a monocular one. As described in the last chapter of the previous article (Hirai and Fukushima, 1975), when a binocular pair of input patterns consist of, for example, many vertical bars placed very closely to each other, the binocular depth neurons might respond not only to correct binocular pairs, but also to incorrect ones. Our present study is concentrated upon how the visual system finds correct binocular pairs or binocular correspondence. It is assumed that some neural network is cascaded after the binocular depth neurons and finds out correct binocular correspondence by eliminating the incorrect binocular pairs. In this article a model of such neural network is proposed. The performance of the model has been simulated on a digital computer. The results of the computer simulation show that this model finds binocular correspondence satisfactorily. It has been demonstrated by the computer simulation that this model also explains the mechanism of the hysteresis in the binocular depth perception reported by Fender and Julesz (1967).

Computers↗
PubMed1977

Perceived lightness depends on perceived spatial arrangement.

The perceived shade of gray depends primarily on the luminance relationship between surfaces percieved to lie in the same plane and not between surfaces that are merely adjacent in the retinal image. This result implies that depth perception must precede lightness perception and that lateral inhibition cannot explain lightness constancy.

Depth Perception↗
PubMed1992

Using stereokinetic effect to convey depth: computationally efficient depth-from-motion displays.

Recent developments in microelectronics have encouraged the use of 3D data bases to create compelling volumetric renderings of graphical objects. However, even with the computational capabilities of current-generation graphical systems, real-time displays of such objects are difficult, particularly when dynamic spatial transformations are involved. In this paper we discuss a type of visual stimulus (the stereokinetic effect display) that is computationally far less complex than a true three-dimensional transformation but yields an equally compelling depth impression, often perceptually indiscriminable from the true spatial transformation. Several possible applications for this technique are discussed (e.g., animating contour maps and air traffic control displays so as to evoke accurate depth percepts).

Aircraft↗
PubMed1992

Occlusion as a depth cue in the Wheatstone-Panum limiting case.

We examined the hypothesis (Ono & Wade, 1985) that occlusion of far stimuli by a near one on the same visual line can operate as a depth cue in stereograms containing different numbers of targets in the two eyes. By controlling eye positions, we created conditions in which the visual system could interpret the retinal images as originating from stimuli on the visual axis of one eye and also created other conditions in which the origin of the retinal images was ambiguous. In Experiment 1, we presented two lines to one eye and a single line to the other eye. When the image of the line on the temporal side of the line pair on one retina fused with the image of the single line on the other retina, the nonfused line appeared farther away more often than it did when the image on the nasal side fused. In Experiment 2, we used two differently shaped stimuli. In the condition in which the nonfused stimulus represented an object being occluded, it appeared farther away more often than in the four conditions in which it did not. In Experiment 3, we extended the idea to three different objects. When the middle of the three images fused with the single image, the nonfused stimulus appeared farther when it could be interpreted as being occluded than when it could not. In the condition in which the most temporal image fused with the single image, the nonfused stimuli appeared farther than in the condition in which the most nasal one fused. The results supported the hypothesis that occlusion plays a role in depth perception in the Wheatstone-Panum limiting case.

Adult↗
PubMed1976

Pictorial depth sensitivity in two-year-old children.

2-year-old children's pointing responses to the closer or farther of 2 pictured houses were consistently accurate when the depth information included either interposition or relative height in the picture plane. Picture-plane size was not an effective source of depth information. These results place the emergences of pictorial depth perception prior to 20 months of age for children with previous exposure to pictures.

Age Factors↗
PubMed1992

Learning to see random-dot stereograms.

In the present study some specific properties of the learning effects reported for random-dot stereograms are examined. In experiment 1 the retinal position-specific learning effect was reproduced and in a follow-up experiment it was shown that the position specificity of learning can be accounted for by selective visual attention. In experiments 2 and 3 evidence was obtained that suggests that observers can learn, to a certain degree, monocular random-dot patterns and that this learning facilitates the depth percept. This result indicates that the traditional belief that random-dot stereograms are devoid of monocularly recognizable or useful forms should be reconsidered. In the second set of experiments the learning of two binocular surface properties of random-dot stereograms, depth edges and internal depth regions, was investigated. It was shown in experiment 4 that the depth edges of random-dot stereograms are not learned, whereas the results of experiment 5 indicate that the internal depth regions are learned. Finally, in experiment 6 it was shown that depth edges are learned when the internal depth regions of the stereogram are ambiguous. The results are discussed in terms of the importance of the particular type of stimulus used in the learning process and in terms of perceptual learning and attention.

Attention↗
PubMed1992

Human stereopsis.

This paper reviews much of the basic literature on stereopsis for the purpose of providing information about the ability of humans to utilize stereoscopic information under operational conditions. This review is organized around five functional topics that may be important for the design of many stereoscopic display systems: geometry of stereoscopic depth perception, visual persistence, perceptual interaction among stereoscopic stimuli, neurophysiology of stereopsis, and theoretical considerations. The paper concludes with the presentation of several basic ideas related to the design of stereoscopic displays.

Animals↗
PubMed1977

Experience and latency to achieve stereopsis: a replication.

This study replicated and extended the findings of MacCracken and Hayes (1976). 10 students were presented the same complex stereogram for 5 trials daily over 2 nonconsecutive days, and latencies to achieve depth perception were recorded. Latencies decreased across 5 trials in the first session but were somewhat longer at the beginning of the second session than at the end of the first session.

Adolescent↗
PubMed1978

[Unilateral aphakia and pseudophakia].

Aniseikonia as well as binocular vision and depth perception are measured in 114 patients with unilateral pseudophakos. 86% of the cases exhibit a small degree of aniseikonia (3% or less). However, binocular vision and stereopsis remain subnormal or approximatively normal.

Adolescent↗
PubMed1977

Stereopsis in the falcon.

Stereoscopic depth perception is demonstrated in the falcon, a non-mammalian with binocular vision. This result complements recent physiological evidence for binocular interaction in the bird visual system, and suggests that stereopsis may be a general attribute of vertebrate vision and not an exclusive product of mammalian evolution.

Animals↗
PubMed1992

Common region: a new principle of perceptual grouping.

A new principle of grouping is proposed that is based on elements being located within a common region of space. Demonstrations analogous to Wertheimer's original displays show that this factor strongly influences perceived grouping and is capable of overcoming the effects of other powerful grouping factors such as proximity and similarity. Grouping by common region is further shown to depend on perceived depth relations, indicating that it is influenced by processes that occur after at least some depth perception has been achieved. Further demonstrations suggest that it is dominated by the smallest background area and that it can follow a hierarchical embedding scheme. It is argued that common region cannot be reduced to the effects of proximity, closure, or any other previously known factor and therefore constitutes a genuinely new principle of grouping.

Depth Perception↗
PubMed1992

Prevalence of disabled stereopsis in a class of optometry students.

Stereopsis is said to be disabled when the third dimension (3-D) cannot be perceived during everyday life but can be when viewing conditions are appropriately arranged. To discover a test suitable for detecting disabled stereopsis, I measured stereoacuity, stereolatency, and the subjective difference in depth perception between monocular and binocular vision of a group of 41 optometry students. Only 2 students showed no sign of this disability. A predictive value for each test was calculated from the results of 14 students whose disability was confirmed by another means. Stereoacuity had the worst predictive value (43%) and stereolatency the best (100%). The prevalence of disabled stereopsis in this group was no less than 34% and might have been as great as 95%.

Depth Perception↗
PubMed1976

[The 3- and 4-point experiments and a test of homogeneity in binocular visual space (author's transl)].

The variability of the 2 parameters in the Luneburg model, sigma (the degree of depth perception) and K (the curvature of binocular visual space), was examined. The 3- and 4-point experiments were performed to estimate these parameters by using various sized stimulus configurations. For 2 of the Os used, it was found that the value of K was inversely related to the size of stimulus configuration (SSC) while the value of sigma was constant. This finding was discussed referring to previous investigations and problems: The discrepancy in the estimated values of K between the alley experiment and 3- and 4-point experiments, equidistance tendency, and angular separation problem in the traditional size constancy experiment.

Depth Perception↗
PubMed1975

Behavioral study of the visual cortex of Galago senegalensis.

An ablation study of the visual cortex of Galago senegalensis was undertaken in the hope of finding clues about the evolution of primate visual cortex. Removal of area 17 resulted in a profound sensory loss manifested by, first, the failure to discriminate between simple patterns; second, a deficit in localizing objects; third, a deficiency in tracking moving objects; and fourth, symptoms attributable to a deficiency in depth perception, such as misreaching and inaccurate jumping. Thus, the effects of ablating area 17 are similar in bushbabies and monkeys. In contrast, minimal sensory loss is produced by ablating area 17 in squirrels or tree shrews. This difference between primates and other mammals may depend on differences in the extent of the cortical target of the tecto-pulvinar path; in Galago and perhaps in all primates, more of the extrastriate visual cortex is entirely dependent on area 17. Removal of the ventral temporal cortex resulted in a loss of learned visual discriminations and in retardation in learning new visual discriminations. These symptoms seem related to the inferotemporal syndrome in monkeys.

Animals↗