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At least 19 recordsLinked to original sources
PubMed1989

Depth perception in cats after cerebral hemispherectomy: comparisons between neonatal- and adult-lesioned animals.

Depth perception was studied in adult cats following removal of the left cerebral hemisphere as a neonate or as an adult. Both monocular and binocular thresholds were determined using a visual cliff. Although both age-at-lesion groups showed depth perception deficits, the neonatal-lesioned animals performed much worse under binocular conditions on the visual cliff than either adult-lesioned or intact animals. This was primarily due to the lack of a binocular advantage in the neonatal-lesioned cats since their monocular thresholds were similar to that of adult-lesioned animals. Both lesioned groups showed higher monocular thresholds compared to intact animals but this effect reached significance only for the right eye. In addition, the neonatal-lesioned cats showed ocular misalignment which may have contributed to their lack of binocular depth perception. Regardless of these deficits neonatal-lesioned cats were more like intact controls regarding the types of errors made on the visual cliff. Neonatal-lesioned animals and intact controls made random errors, whereas adult-lesioned animals made most of their errors when the shallow shelf was presented on the animals' right side. This may indicate that the adult-lesioned animals have greater motor and/or visual field biases than do neonatal-lesioned cats.

Aging↗
PubMed1979

Influence of sonic noise on human stereoscopic depth perception.

Scientific establishment of the no-effect response to finite levels of exposure to a physical or chemical agent is indeed a rigorous exercise and is frequently controversial. In earlier research by Slutsky under direction of the senior author, a statistically significant increase in stereoscopic depth perception error was noted among 24 test subjects exposed to high intensity noise. Additional extensive research reported in this paper indicates that error in stereoscopic depth perception is not significantly altered by exposure to continuous white noise of short duration at levels ranging from 70 to 115 dBA. Furthernore, exposure of humans for periods of a few minutes to white noise in octave bands centered on 250 Hz, 1000 Hz, 4 kHz and 16 kHz at 115 dB does not affect their depth perception measured by the Howard-Dolman test. A comprehensive analysis of depth perception errors measured under noise exposure conditions (n = 4040) in comparison with those obtained under control conditions (n = 1430) produced a mean change in error of -0.38 mm, a statistically insignificant difference (p = 0.17). Even if such an error were attributable to high level noise, it should be noted that minus sign designates an improvement of depth perception in noise and that it is difficult to imagine visual tasks in which change in error of +/-0.38 mm at a distance of 6.0 meters is meaningful.

Depth Perception↗
PubMed1989

Depth perception after prolonged usage of night vision goggles.

The present study was initiated following a report that a few helicopter pilots had failed a test of stereoscopic depth perception after a prolonged training flight employing night vision goggles (NVGs). In order to determine the cause of the loss, 12 helicopter pilots/copilots were assessed for depth perception, lateral and vertical phoria, and contrast sensitivity before and after training flights requiring the pilots to wear night vision goggles for the duration of the flight. Pilots flew one to three missions while wearing either PVS-5A or AN/AVS-6 goggles. Mission duration ranged from 1 to 4 h. The results indicate that contrast sensitivity and depth perception when monocular cues are present did not degrade over the course of the mission. Lateral phoria, however, did demonstrate an average exophoric shift of 1.5 prism diopters for 12 out of the 24 missions. The results indicate that the original report of a loss of depth perception based on a test of depth requiring stereopsis might have been caused by a shift in lateral phoria. It would be expected that as additional fusional effort is required, the minimum resolvable disparity degrades due to the increase in accommodation brought about through vergence accommodation. Possible causes for the phoria shift and future testing are discussed.

Accommodation, Ocular↗
PubMed1975

Depth perception and location of brain lesions.

Depth perception was examined in 50 patients with brain lesions and in 16 controls using a polaroid test (Titmus). Error percentage and response time were measured. Intellectually impaired patients performed significantly worse than intellectually normal patients. On the other hand, location of the cerebral lesion (right, left, or generalized) had no significant effect; zero error percentages were observed among intellectually normal patients even with right or left parietal lesions. Intellectually normal patients did not differ from healthy controls.

Brain Diseases↗
PubMed1992

[Depth perception and amplitude of VEPs for variations of dot density in static random dot stereograms].

Relative changes in depth perception and amplitude of VEPs were compared when the dot density in static random dot stereograms was altered. The maximum amplitudes of negative potentials evoked by either stereogram or uncorrelogram were recorded from the occipital region of human scalp. The peak latency was in the range of 160 to 260 msec, averaging 197 msec in 18 subjects. The amplitude of negative potentials evoked by either stereogram or uncorrelogram was always larger than that evoked by correlogram. The amplitudes on either stereograms, uncorrelograms or correlograms did not significantly increase when the dot density was increased, and there was no significant difference in amplitude on either stereogram or uncorrelogram. Depth perception did not closely correlate with the dot density nor with the amplitude of negative potentials. These results suggest that the amplitude of negative potentials may represent activities of disparity-sensitive neurons elicited in a trigger feature manner, but it does not reflect activities of the higher order process of depth perception.

Adult↗
PubMed1978

Paradoxical sleep and depth perception.

It has been hypothesised that one possible function of paradoxical (REM) sleep is the maintenance of facilitation of co-ordinated eye movements. A prediction from this hypothesis is that binocular depth perception will be more accurate at the end of periods of paradoxical sleep than at the beginning. The results from previous studies are conflicting. Using two groups of eight healthy male volunteers in a two factor repeated measures design, it was found that for a period of paradoxical sleep in the second half of the night only, there was an improvement in binocular depth perception accuracy between the beginning and end of paradoxical sleep. The accuracy at the end of the paradoxical sleep was not significantly different to that on going to bed or on awakening in the morning; the effect was due to a large decrease in accuracy at the start of the REM period. There was no effect of paradoxical sleep on binocular depth perception in the early part of the night. Monocular depth perception accuracy was unaffected by paradoxical sleep.

Adolescent↗
PubMed1989

Amphetamine-induced recovery of visual cliff performance after bilateral visual cortex ablation in cats: measurements of depth perception thresholds.

After bilateral visual cortex ablation, cats exhibit a loss of depth perception as measured on a visual cliff, which recovers following administration of d-amphetamine. In this Study, 3 amphetamine-treated cats with visual cortex ablations showed a rapid and enduring recovery, with 2 of these animals obtaining levels of performance seen only with binocular vision, suggesting a restoration of binocular depth perception. Cats with asymmetrical lesions showed only a transient improvement during amphetamine treatment, and some animals not displaying autonomic signs of amphetamine intoxication did not improve. Saline-treated cats showed no signs of improvement, and the effect of amphetamine was blocked by the catecholaminergic antagonist haloperidol. These results indicate that amphetamine can induce an enduring recovery from a behavioral deficit after brain injury, which if left untreated would not spontaneously recover.

Amphetamine↗
PubMed1989

Binocular depth perception, visual acuity and visual fields in cats following neonatal section of the optic chiasm.

We studied the role of the transcallosal pathway in stereopsis by measuring binocular and monocular depth perception in two cats that had undergone section of the optic chiasm at the age of 21 d. To ensure that the surgery did not impair vision to the extent that depth perception could not be evaluated, visual acuity and visual fields were also measured. In both of the chiasm-sectioned animals the visual fields were reduced and the visual acuity was substantially lower than in normal cats, with a maximum of about 2 cyc deg-1. Binocular depth thresholds of the chiasm-sectioned cats were worse than those of the normal cat but were better than their own monocular thresholds. These results suggest that the chiasm-sectioned animals were still able to use binocular cues to judge depth and indicate that the indirect pathway through the corpus callosum is sufficient to mediate binocular depth perception.

Depth Perception↗
PubMed1991

Influence of remote objects on local depth perception.

The perceived relative depth of two test dots displayed within the fovea is shown to be influenced by other features in the surrounding area. These features can be as far apart as 51 deg and can have relative disparities as large as 20 deg, much larger than the disparities of the test dots. Since this effect is seen for stimuli presented for 100 msec or less, changes in direction of gaze cannot play a role. The effect varies inversely as the spatial separation between the test dots and the remote features, and is insensitive to the relative disparities of these remote features when they are greater than 2 deg. Observers sometimes differ significantly from each other in their responses to various configurations of the outlying features. This appears to rule out response mechanisms which depend only on the stimulus; some characteristics of the observer must be involved in determining the response. For these briefly presented stimuli, observers are unable to report accurately the relative depth of the central foveated test items if they are also required to report the depths of distant peripheral features.

Depth Perception↗
PubMed1992

Shape analysis and stereopsis for human depth perception.

The perceived relative depth of two isolated short parallel lines in the center of a scene is known to depend on the disparities and positions of other items in the scene, as well as on their own disparities. We demonstrate here that the shapes of these other items also contribute significantly to the perceived depth, and that these non-disparity influences on depth judgements may already be evident when only three dots are presented as stimuli. When two short vertical test lines are surrounded by a trapezoidal "picture frame", the perceived relative depth of the test lines is affected by the shape of the trapezoid as well as by the disparities assigned to its vertical parallel sides. The influence of the trapezoidal frame can be interpreted as an effect of perspective. The induced relative depth of the test lines is measured by recording the amount of "compensating disparity" that must be given to one of the lines in order for observers to judge the two test lines to be equidistant from the observer's viewing position. Surprisingly, for fixed disparities of the vertical edges of the surrounding picture frame, the induced depth of the test lines increases as the difference in the lengths of the vertical sides increases, regardless of whether the perspective interpretation of the difference in the lengths is consistent with or in conflict with the disparity-defined slant. Shape-related apparent depth changes are especially sensitive to the shape of the trapezoid if it is nearly rectangular, and are comparable in magnitude to those resulting from changes in disparity of the surrounding frame. When a pair of short vertical parallel test lines is presented alone, without a surrounding frame or any other items in the scene, excellent relative depth discrimination is displayed by most subjects. However, if the lines are replaced by squares, trapezoids, triangles, single horizontal lines, or other figures of about the same size as the original test lines, the slant discrimination threshold for these plane figures for naïve observers become poorer by a factor of 20-100. By the use of a feedback signal, observers can be trained to use only disparity cues and ignore shape effects. Some observers have difficulty ignoring the shapes of some figures, the "difficult" figures being different for each observer. After training, the relative depth thresholds for most figures approach those of the original unconnected parallel test lines.

Depth Perception↗
PubMed1991

Temporal limits of the susceptibility of depth perception to proprioceptive deafferentations of extraocular muscles.

In a previous study, extraocular muscle proprioception (E.O.M.P.) was shown to play an important role in the postnatal development of depth perception: following unilateral or bilateral sections of the ophthalmic branch of the trigeminal nerve (V1th nerve) performed at 6-8 weeks of age, the binocular thresholds were 2 to 3 times higher than in control animals. Since the V1-sections produced no deficits when performed in adults, the temporal limits of a period of susceptibility remained to be determined. In order to assess the lower and upper limits of the period during which these perceptual deficits could be induced, unilateral or bilateral V1-sections were performed in kittens at different ages. Depth perception thresholds were measured by using the jumping stand technique. Sections of the V1 nerve only produced significant impairments of the binocular depth thresholds when performed after 3 weeks of age. They could be observed when unilateral sections were performed at up to 13 weeks of age and with bilateral sections at up to 10 weeks of age. These functional impairments appeared to remain permanently through adult life.

Animals↗
PubMed1979

Assessment of depth perception in cats.

A behavioural method is described for the assessment of depth perception of kittens. Measurement is made of the smallest separation in depth that can be discriminated between two adjacent stimuli under both monocular and binocular viewing conditions. Normal animals can discriminate much smaller separations in depth when using two eyes than with monocular viewing, implying the presence of a cue to depth that is uniquely available with binocular viewing. The test provides a quick and reliable way of screening animals for stereopsis.

Animals↗
PubMed1992

Factors that affect depth perception in stereoscopic displays.

This study investigated several factors that affect depth perception in stereoscopic displays: half-image separation magnitude, separation direction (crossed vs. uncrossed), viewing distance, stimulus size, and exposure duration. The depth perceived under various combinations of levels of these factors was compared with depth predicted by the geometry of stereopsis. Perceived depth in the crossed-separation direction was frequently close to predictions, such that increases in separation and viewing distance produced appropriate increases in perceived depth. Depth in the uncrossed direction was frequently less than that predicted, especially for small stimuli presented at a long viewing distance, with a large half-image separation, and/or with a brief duration. Thus depth in both crossed and uncrossed directions equaled predictions only for large stimuli exposed for a long duration.

Adult↗
PubMed1992

Stereolatency: a stereopsis test for everyday depth perception.

An instrument is described which tests for the use of stereopsis by measuring how long it takes for depth perception to begin (its latency) after a transition from monocular to binocular vision. Starting at 1 s, the duration of binocular vision is reduced progressively toward a limit of 16 ms (or increased to a limit of 4 s) until the latency of stereopsis is found. The preliminary period of monocular vision acts as a probe for suppression of either eye and allows time for accommodation and vergence to stabilize before binocular vision begins. Typical results are presented.

Depth Perception↗
PubMed1992

Clinical measurement of depth perception by means of motion parallax: a case report.

An automated 2-rod stereoacuity test was modified to permit lateral head movement during testing so that depth perception by means of motion parallax could be assessed. The patient, a 48-year-old truck driver with one blind eye, found the test easy to perform. In 24 presentations of a 40 sec arc disparity he was 96% correct. With the same number of presentations at 20 sec arc he was 83% correct. In the latter case, the probability of success by chance alone was p = 0.0004.

Depth Perception↗
PubMed1991

Depth perception and cortical physiology in normal and innate microstrabismic cats.

Evidence is presented that innate microstrabismus and abnormal cortical visual receptive-field properties can occur also in cats without any apparent involvement of the Siamese or albino genetic abnormalities in their visual system. A possible cause for microstrabismus in these cats may be sought in an abnormally large horizontal distance between blind spot and area centralis indicated by a temporal displacement of the most central receptive fields on both retinae. Depth perception was found to be impaired in cats with innate microstrabismus. Behavioral measurements using a Y-maze revealed in four such cats that the performance in recognizing the nearer of two random-dot patterns did not improve when they were allowed to use both eyes instead of only one. The ability of microstrabismic cats to perceive depth under binocular viewing conditions only corresponded to the monocular performance of five normal cats. Electrophysiological recordings were performed in the visual cortex (areas 17 and 18) of four awake cats, two normal, and two innate microstrabismic animals. Ocular dominance and orientation tuning of single neurons in area 17 and 18 were analyzed quantitatively. The percentage of neurons in area 17 and 18 which could be activated through either eye was significantly reduced to 49.7% in the microstrabismic animals when compared to the normal cats (74.8%). "True binocular cells," which can only be activated by simultaneous stimulation of both eyes, were significantly less frequent (1.6%) in microstrabismic cats than in normal animals (10.4%). However, subthreshold binocular interactions were identical in both groups of animals. In the strabismic animals, long-term binocular stimulation of monocular neurons did not give a clear indication of alternating use of one or the other eye. The range of stimulus orientations leading to discharge rates above 50% of the maximal response, i.e. the half-width of the orientation tuning curves, was the same in the two groups of cats. However, orientation sensitivity, i.e. the alternation in discharge rate per degree change in stimulus orientation, was higher in cortical cells of normal cats than in those of microstrabismic cats. In normal and microstrabismic cats, no clear sign of an "oblique effect," i.e. the preference of cortical neurons for vertical and horizontal orientations compared to oblique orientations, could be found neither in the incidence of cells with horizontal or vertical preferred orientation nor in the sharpness of orientation tuning and sensitivity of these neurons.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗