PubMed Health⌕ Search

SEARCH · PubMed Health

Results for “Form Perception”

Explore indexed PubMed citations for clinical trials, systematic reviews and public health research. Read source abstracts and follow each citation to its original PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 703 records · Page 39Linked to original sources

Is orientation-specific color adaptation in human vision due to edge detectors, afterimages, or "dipoles"?

After one looks alternately at red vertical and green horizontal stripes, vertical and horizontal white stripes appear greenish and pink, respectively. This color aftereffect might imply that contour-detecting cells participate in human vision, or might simply be due to afterimages. A procedure that precludes afterimages still yields aftereffects, but sensory units less complex than edge detectors could be responsible.

Afterimage↗

Visual spatial illusions: a general explanation.

Representation at the visual receptors of such properties of the object as its size, shape, orientation, and movement undergo considerable variation as the distance, bearing, posture, and motion of the observer, relative to the object, changes. However, despite these gross and frequent deformations of the image, perceived properties remain extraordinarily stable. Such constancy has obvious biological utility; the observer perceives his world according to its fixed physicalfeatures rather than in terms of its variable sensory representation. Constancy of apparent size, shape, orientation, and movement is dependent on information for the distance, bearing, lateral tilt, and movement of the observer, respectively. Thus, as the retinal image shrinks with distance, constancy of apparent size is maintained by five classes of distance, stimuli that operate singly or in various combinations. Likewise, visual orientation and visual stimuli for the orientation of the observer, and movement constancy on visual and nonvisual stimuli for the movement of the observer. Illusion occur when stimuli that normally preserve constancy are operative but with the image of the object not varied. Thus if retinal disparity, convergence-accommodation, projected stimuli, or other distance stimuli are varied with the image not varied, illusions of size occur. Those rsluting from variation of projected stimuli are the. well-known geometrical size illusions and include the Mü llerLyer group. In essentially the same manner, independent manipulation of stimuli for the orientation and the motion of the observer, with the orientation and the motion of the image at the retina not varied, gives rise to illusory orientations and movements of the object. Limited attempts to explain size illusions in terms of the projected stimuli that preserve perceptual constancy are by no means new; Thiéry (51) proposed such a view in the later part of the last century, and in recent times there has been a spate of such proposals including the " misapplied constancy hypothesis" advanced by Gregory (2). However, Gregory's theory is confined largely to geometrical size illusions and invoks only distance scaling given by a limited number of projected stimuli. Furthermore, the Müller-Lyer illusion is seen by him to be a consequence of distance scaling resulting from the converging arrows. There is no recognition of the range of such effects with various attached elements, as shown in Fig3, and no attention is accorded the recently established difference between the illusions with inward and outward-directed elements. The theory of spatial illusions outlined here distinguishes between classes of illusory effect and, in linking each to its particular class of spatial constancy, offers a general and testable explanation. Failure to recognize classes of illusion(and perceptual constancy), such as those of size, orientation, and movement, can be regarded as among the major deficiencies of recent attempts (2, 44) to explain illusory effects. I do not claim that this explanation, which I call the general constancy theory, satisfactorily encómpasses all known illusions, but merely that it is more comprehensive than alternative explantions I conclude that any stimulus which serves to maintain perceptual constancy of a property of an object as the visual representation of that property varies will, when independently manipulated with the retinal image not varied, produce an illusion. This general principle predictS the conditions under which illusory effects will occur and has wide explanatory application.

Age Factors↗

Steroscopic vision: cortical limitations and a disparity scaling effect.

The spatial limitations of stereoscopic vision were studied by using vertical line stimuli containing sinusoidal disparity variations such that different parts of the line appeared at different depths. Stimuli with a finer grain than about 3 cycles per degree did not elicit depth perception, even though the sinusoidal curvature was clearly visible monocularly. At low spatial frequencies of curvature, stereoacuity was limited to the same extent as the monocular sensitivity. The limiting disparity for Panum's fusional region and the upper depth limit are subject to a scaling effect in proportion to stimulus dimensions. The disparity scaling can be characterized by a fixed maximum angular difference between the parts of the stereoscopic half-images.

Depth Perception↗

The role of the primate extrastriate area V4 in vision.

Area V4 is a part of the primate visual cortex. Its role in vision has been extensively debated. Inferences about the functions of this area have now been made by examination of a broad range of visual capacities after ablation of V4 in rhesus monkeys. The results obtained suggest that this area is involved in more complex aspects of visual information processing than had previously been suggested. Monkeys had particularly severe deficits in situations where the task was to select target stimuli that had a lower contrast, smaller size, or slower rate of motion than the array of comparison stimuli from which they had to be discriminated. Extensive training on each specific task resulted in improved performance. However, after V4 ablation, the monkeys could not generalize the specific task to new stimulus configurations and to new spatial locations.

Animals↗

Color and luminance: independent frequency shifts.

Simultaneous opposite spatial frequency shifts can be obtained in chrominance and luminance channels. The chrominance shift cannot be transferred interocularly. Chrominance and luminance channels seem to perform similar but independent spatial frequency analyses.

Color Perception↗

Spatial adaptation of short-wavelength pathways in humans.

Color-selective spatial adaptation of the short-wavelength, or blue-sensitive, pathway was demonstrated. The adaptation was orientation selective and strongly monocular. Adaptation was assessed by measuring visibility thresholds for monochromatic gratings in subjects adapted to high-contrast violet gratings designed to stimulate only blue-sensitive cones. The results showed spatially selective, adaptable channels within the short-wavelength pathway.

Adaptation, Physiological↗

Visual aftereffects derived from inspection of orthogonally moving patterns.

Alternate inspection of patterns moving in orthogonal directions induces an aftereffect in which a stationary test pattern seems to move in a new direction. This direction is the resultant of the two directions of aftereffect that would have arisen from separately inspecting each of the moving patterns. The direction in which objects appear to move, like their color and depth, can thus depend on a synthesis of unperceived components.

Afterimage↗

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↗

Investigating human color preferences in the perception of complex three-dimensional structures.

This article describes preliminary results of a investigation that addresses the problem of human color perception in the visual analysis of complex three-dimensional shapes. We built 3D visualization models of synthetic neural cells, and designed two experiments to identify user preferences for color when observing and executing tasks on these 3D models. Though preliminary, the results obtained from these experiments are consistent and indicate that some trends exist that deserve further investigation.

Color Perception↗

Event perception.

Explore the source record for details and available documents.

Blindness↗

Role of primate visual area V4 in the processing of 3-D shape characteristics defined by disparity.

We studied the responses of V4 neurons in awake, fixating monkeys to a diverse set of stereoscopic stimuli, including zero-order disparity (frontoparallel) stimuli, surfaces oriented in depth, and convex and concave shapes presented at various mean disparities. The responses of many V4 cells were significantly modulated across each of these stimulus subsets. In general, V4 cells were broadly tuned for zero-order disparity, and at any given disparity value, about four-fifths of the cells responded significantly above background. The response modulation by flat surfaces oriented in depth was significant for about one-quarter of cells, and the responses of about one-third of the cells were significantly modulated by convex or concave surfaces at various mean disparities. However, we encountered no cells that unambiguously distinguished a given three-dimensional (3-D) shape independent of mean disparity. Thus 3-D shapes defined by disparity are unlikely to be represented explicitly at the level of individual V4 cells. Nonetheless, V4 cells likely play an important role in the processing of 3-D shape characteristics defined by disparity as a part of a distributed network.

Analysis of Variance↗

Receptive field properties of single neurons in rat primary visual cortex.

The rat is used widely to study various aspects of vision including developmental events and numerous pathologies, but surprisingly little is known about the functional properties of single neurons in the rat primary visual cortex (V1). These were investigated in the anesthetized (Hypnorm-Hypnovel), paralyzed animal by presenting gratings of different orientations, spatial and temporal frequencies, dimensions, and contrasts. Stimulus presentation and data collection were automated. Most neurons (190/205) showed sharply tuned (</=30 degrees bandwidth at half height) orientation selectivity with a bias for horizontal stimuli (31%). Analysis of response modulation of oriented cells showed a bimodal distribution consistent with the distinction between simple and complex cell types. Orientation specific interactions occurred between the center and the periphery of receptive fields, usually resulting in strong inhibition to center stimulation when both stimuli had the same orientation. There was no evidence for orientation columns nor for orderly change in optimal orientation with tangential tracks through V1. Responses were elicited by spatial frequencies ranging from zero (no grating) to 1.2 cycle/degree (c/ degrees ), peaking at 0.1 c/ degrees, and with a modal cutoff of 0.6 c/ degrees. Half of the neurons responded optimally to drifting gratings rather than flashing uniform field stimuli. Directional preference was seen for 59% of oriented units at all depths in the cortex. Optimal stimuli velocities varied from 10 to 250 degrees /s. Some units, mainly confined to layer 4, responded to velocities as high as 700 degrees /s. Response versus contrast curves (best fit with Naka-Rushton) varied from nearly linear to extremely steep (mean contrast semisaturation 50% and threshold 6%). There was a trend for cells from superficial layers to be more selective to different stimulus parameters than deeper layers cells. We conclude that neurons in rat V1 have complex and diverse visual properties, necessary for precise visual form perception with low spatial resolution.

Animals↗

Effects of selective attention on perceptual filling-in.

After few seconds, a figure steadily presented in peripheral vision becomes perceptually filled-in by its background, as if it "disappeared". We report that directing attention to the color, shape, or location of a figure increased the probability of perceiving filling-in compared to unattended figures, without modifying the time required for filling-in. This effect could be augmented by boosting attention. Furthermore, the frequency distribution of filling-in response times for attended figures could be predicted by multiplying the frequencies of response times for unattended figures with a constant. We propose that, after failure of figure-ground segregation, the neural interpolation processes that produce perceptual filling-in are enhanced in attended figure regions. As filling-in processes are involved in surface perception, the present study demonstrates that even very early visual processes are subject to modulation by cognitive factors.

Adult↗

Does luminance contrast determine lightness?

When presented against a highly lit black background, dimly illuminated white paper strips appear white even when they are equiluminant with the background. Such an example of simultaneous lightness constancy cannot be accounted for by receptor gain control because of the equiluminance. Moreover, this demonstration shows that lightness cannot be reduced to 'relative brightness' as is widely believed.

Computer Simulation↗

Fast noninertial shifts of attention.

It was suggested that some discrimination tasks (e.g. discrimination between the letters T and L) require serial search by scrutinizing each letter (target) with a small aperture of focal attention. Here we examine the effect of intertarget distance on discrimination performance, using two targets. We find reduction in performance at short distances, in agreement with masking studies, but constant performance independent of distance outside this masking region. This constant performance is still lower than expected from masking effects and might reflect attentive process. Sequential presentation of the targets with delays up to 30-40 ms, while reducing available processing time, does not cause reduction in performance, thus supporting the suggestion that discrimination of the two targets is a serial process. The independence of performance on distance suggests fast noninertial shifts of attention.

Attention↗