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At least 523 records · Page 29Linked to original sources
PubMed1983

Differential drawing size associated with unilateral brain damage.

Size of Greek Cross reproductions was compared using 35 persons having unilateral right (RHD), 35 having unilateral left (LHD) hemisphere damage and 38 non-neurologic controls. With right hand tapping speed statistically controlled, RHD drawings were significantly larger than LHD reproductions. Spatial Relations scores were significantly associated with drawing size in the RHD group only, following adjustment for right hand tapping speed. Aphasia Screening scores were unrelated to drawing size. These data demonstrate that LHD/RHD drawing size differences are independent of any basic motor impairment and that for RHD subjects, drawing size is positively correlated with visuospatial impairment.

Adult↗
PubMed1991

Figural modulation of visuo-spatial neglect: a case study.

We report a case of severe left visuo-spatial neglect consequent upon right-hemisphere stroke. In Experiment 1, horizontal and vertical (radial) line bisection is performed; the patient displays left neglect and "altitudinal" (radial) neglect, placing his transections too far to the right and to the top, respectively. In Experiment 2, the patient is required to place a dot at the centre of squares and circles, the horizontal and vertical extents of which are identical to the length of the lines employed in Experiment 1. Performance is now extremely accurate. In Experiment 3, the height of the rectangular or elliptical figure whose midpoint is to be estimated is held constant whilst length varies. In Experiment 4, the length of the figure is held constant whilst height is varied. Both manipulations exert a profound, lawful influence on the patient's estimate of each figure's midpoint. We provide some preliminary hypotheses concerning how configurational constraints may affect perceptual and attentional processes in visual neglect.

Attention↗
PubMed1996

Spatial locations gone awry: object and spatial memory deficits in children with fetal alcohol syndrome.

Hippocampus vulnerability following gestational alcohol exposure has been demonstrated neuroanatomically and behaviorally in animal models of fetal alcohol syndrome (FAS). There has been no similar demonstrations in humans. The Smith and Milner (1981) Memory for 16 Objects task has been used to explore the effects of right vs left temporal lobectomy with varying degrees of damage to the hippocampus. In the present experiment, this same task was administered to 15 children with FAS (mean age 10.03, S.D. = 2.33) and 15 control children (mean age 10.02, S.D. = 2.31). Similar to patients with right temporal lobectomies and a large excision to the hippocampus, children with FAS were able to perform immediate but not delayed object recall, had a general spatial memory deficit (P < 0.05), and significantly distorted the spatial array (P < 0.05). Although these results are consistent with an interpretation of hippocampal dysfunction, gestational alcohol exposure is known to result in a wide-ranging spectrum of neuropsychological deficits that vary in both extent and severity. Visuospatial deficits on the Beery test of Visuomotor Integration and Clock Drawing are suggestive of the other neural regions that may be involved in producing the behavioral deficits in children with FAS.

Adolescent↗
PubMed1982

The dependence of the induced effect on orientation and a hypothesis concerning disparity computations in general.

The induced size effect is an apparent rotation about a vertical axis that results from binocularly viewing a target in which one half-image is vertically magnified. A previous paper (Arditi et al., 1981, Vision Res. 21, 755-764) described a theory of this effect in terms of horizontal disparities that exist between vertically magnified images of oblique features and their unmagnified counterparts. The present studies test two aspects of that theory: the requirement of oblique features in stimuli eliciting the induced effect, and the assumption that binocular associations (inputs to disparity computations) are made across horizontal meridians. The former aspect was confirmed in a stereo discrimination experiment in which the direction of rotation (tilt) for crossed line patterns of varying orientation was judged, for a fixed vertical magnification of one half-image. The latter aspect was rejected on the basis of the results of that experiment, and of two experiments in which observers matched the apparent tilt of the lines with a horizontal adjustment line which could be stereoscopically rotated in depth. The data and some associated demonstrations suggest that stereoacuity and apparent depth of oblique lines vertically magnified in one half-image are determined by the horizontal separation between binocular points which are nearest in a fixed binocular coordinate map, rather than by purely horizontal point-matchings. This "nearest neighbor hypothesis" seems to be operative in classic measures of stereoacuity as well as in the induced effect.

Eye Movements↗
PubMed1982

Contrast sensitivity at high velocities.

Measurements were made of the contrast required to see the direction of motion of drifting gratings (Part 1) and of moving bars (Part 2). The spatial frequency at which least contrast is required to see sinusoidal gratings decreases as their velocity increases, but peak sensitivity is identical at all velocities up to 800 deg/sec. Similarly, the wider a single bar, the higher the velocity at which it is best visible. A bar 80 deg wide is best seen when moving at 300-500 deg/sec, and can be seen, and its direction of motion identified, even when moving at 10(4) deg/sec. These results show that motion does not diminish the visual passband, but instead slides the spatial frequency window along the spatial frequency scale, maintaining peak sensitivity at a temporal frequency of about 10 Hz (at photopic luminances).

Differential Threshold↗
PubMed1989

Visually perceived eye level and perceived elevation of objects: linearly additive influences from visual field pitch and from gravity.

Observing a pitched visual field (i.e. tilted around a horizontal axis in the observer's frontal plane) results in large changes in the elevation visually perceived to correspond to eye level (VPEL) and in the perceived elevation and size of stationary objects viewed against the field. With topforward pitch (top toward observer) VPEL lies above true eye level and objects appear smaller and lower; with topbackward pitch VPEL lies below true eye level and objects appear larger and higher. Oscillation of the pitched field induces synchronous perceived oscillation of elevation of a stationary target viewed against the field. Typical VPEL settings deviated from true eye level by 20 degrees with the field pitched at 40 degrees, although some individuals mislocalized by as much as 40 degrees. VPEL varied linearly with visual field pitch with individual slopes for the relation between VPEL and visual field pitch ranging from +0.42 to +0.78 (avg = +0.56). The linear correlation (r) between VPEL in darkness and against an erect visual field was +0.91. The two relations--VPEL vs visual field pitch, VPEL in darkness vs VPEL in the erect illuminated visual field (slope approximately equal to 0.5)--are both accurately predicted by the linear model: VPEL = kvV + kbB; in which V is the influence of visual field structure and B is the influence of the body-referenced mechanism which combines information regarding the orientation of the head relative to gravity, the position of the eye in the orbit, and the vertical location of the image on the retina; kv and kb are the relative weights of V and B with kv + kb = 1. In an illuminated field kv = kb approximately equal to 0.5; in the dark kv = 0, kb = 1.

Gravitation↗
PubMed1990

Two mechanisms for localization? Evidence for separation-dependent and separation-independent processing of position information.

The Weber function for separation--i.e. delta s as a function of separation s--is typically measured using a pair of targets presented roughly symmetrically relative to the fovea. With this paradigm, as the separation increases, the eccentricity of the individual targets increases also. To disentangle the effects of separation and eccentricity on the Weber function for separation, we systematically examined each of these variables and also examined the effects of target size and exposure duration. Separation discrimination thresholds were measured for average separations from 3 to 6 deg across a wide range of eccentricities, and for eccentricities of 2.5-10 deg for a range of separations. The dependence of threshold on target size was measured by varying the length of the stimuli from 1 to 120 min arc; the dependence on exposure duration was measured using durations of 100 and 500 msec at 10 deg eccentricity for comparison with data collected previously at smaller eccentricities. We found that for separations less than the eccentricity of the targets, thresholds depend primarily on separation; for larger separations, thresholds depend solely on eccentricity. In general, unless the targets are very small or quite brief, the spatial and temporal characteristics of the targets are not major contributors to the slope of the Weber function. Two mechanisms are proposed to account for thresholds in the two regions, one separation-dependent and one separation-independent.

Differential Threshold↗