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At least 127 records · Page 7Linked to original sources
PubMed1986

Areas of spatial interaction for a hyperacuity stimulus.

We report that the ability to detect a small vernier offset (less than 5 sec of arc in many individuals) between two small spots of light separated by a narrow gap can be disrupted by presenting additional targets in close proximity to the vernier stimulus. A rectangular background of light, centered on the vernier stimulus, elevates offset threshold by a factor of two when the total width of the background is 3-4 min arc. Backgrounds narrower or wider than 3-4 min have less or no effect on vernier threshold. These areas of spatial interaction extend to either side of a vertically-oriented vernier stimulus, or above and below a horizontally-oriented stimulus, and their extent is dependent upon the gap size of the two-dot stimulus. The effect of the presence of the background on vernier threshold cannot be accounted for by spatial interval cues nor by changes in the visibility of the stimulus. Two alternative interpretations of the results are presented to develop a description of the underlying mechanisms which produce hyperacuity spatial interactions.

Distance Perception↗
PubMed1986

Shared pathways for rod and cone vision.

We have used heterochromatic gratings falling on 10 deg temporal retina to measure the spatial contrast sensitivities of the isolated rod and cone systems in the mesopic range. As the level of illumination was raised within this range, the contrast sensitivity of the rod system increased, reaching a peak of about 50 (and providing an acuity of 6 c/deg) at 20 scot. td, whereupon the rod system began to saturate. Over most of the mesopic range the sensitivity of the cone system was lower than that of the rod system, although it provided better acuity (up to 15 c/deg). Within the range of spatial frequencies capable of exciting both rod and cone systems, a grating that excited only rods was indistinguishable from a grating of the same spatial frequency that excited only cones. Moreover, contrast adaptation to gratings that excited either rods or cones raised threshold for gratings that excited rods or cones. From these results we conclude that signals from rods and cones travel together in pathways subserving the detection of low spatial frequencies, while only signals from cones travel in pathways subserving the detection of high spatial frequencies.

Adaptation, Ocular↗
PubMed1986

Increment spectral sensitivities for spatial periodic grating patterns: evidence for variable tuning of the chromatic system.

Increment spectral sensitivities were measured for spatial periodic grating patterns. First, the increment threshold was determined as a function of wavelength, for various spatial frequencies and white-background intensities. Second, the additivity of test mixture was tested. Thirdly, the threshold vs intensity curves were determined for various spatial frequencies of test monochromatic stimuli. Finally, the increment threshold was determined as a function of spatial frequency. The following results were obtained: the background intensity and the spatial frequency affected the increment spectral sensitivity functions in different manners; the result of test mixture showed subadditivity for high background intensity and approximately linear additivity for low background intensity; the resultant t.v.i. curves converged toward Weber's law at high background intensity; and the sensitivity vs spatial frequency curve showed a loss of the sensitivity at low spatial frequency for high background intensity. These results called in question the existing hypothesis of separate chromatic and achromatic systems whose spectral tunings are invariant with a spatial parameter, but favored the hypothesis of variable tuning of the chromatic system.

Color Perception↗
PubMed1986

Temporal properties of brightness and color induction.

With a matching procedure, we studied the temporal properties of direct brightness (or lightness) and chromatic changes (produced by modulation of the region being matched) and induced brightness and chromatic changes (produced by modulation of the surround of the region being matched). The amount of direct brightness and color change was found to vary only slightly with temporal frequency over the 0.5-8 Hz range studied, whereas induced changes were found to occur only at low temporal frequencies, below about 2.5 Hz. With high temporal-frequency modulation of the surround, the induced patterns appeared to flicker but not to change in brightness or color. Despite the fact that chrominance and luminance temporal contrast sensitivity functions are very different, the temporal induction curves for color and brightness were very similar. However, brightness induction was found to increase approximately linearly with increasing surround modulation up to very high levels, whereas the amount of color induction was much less dependent on the modulation depth of the surround.

Color Perception↗
PubMed1986

Pre-stereoptic binocular vision in infants.

In a preferential looking experiment, identical patterns (vertical stripes) were presented to both eyes on one of two screens while orthogonal patterns (vertical stripes in one eye and horizontal stripes in the other) were presented on the other screen. Most infants younger than 3.5 months of age originally showed a preference for the dichoptic (interocularly orthogonal) pattern. At an average age of 3.5 months, however, they showed a sudden shift of preference from this pattern to the interocularly identical pattern. The full shift from a preference for one stimulus to the other (both statistically significant) occurred within a few weeks in most cases. The onset age of the shift in preference agreed with the onset age of fusion-rivalry discrimination found in a previous study (Birch et al., 1985). The original preference for the bincularly orthogonal patterns may be interpreted as a preference for a grid (interocularly emergent intersections) over a grating, judging from results of two control experiments. These data suggest that the pre-stereoptic system non-selectively combines information from the two eyes without regard to edge orientation because it loses eye-of-origin information at a relatively early stage of binocular visual processing. Thus, the pre-stereoptic system does not have the capability of interocular suppression. The theoretical and clinical significance of the new findings are discussed along with a neuronal model of cortical development of ocular segregation and binocular pathways.

Adult↗
PubMed1987

Perception of random-dot symmetry and apparent movement at and near isoluminance.

There have been conflicting reports on whether apparent movement in random-dot kinematograms is abolished at isoluminance. The present results suggest that it is, provided that dynamic (uncorrelated) surrounds are used, and the subject has to report the shape of the target rather than the presence of movement in an isolated portion of the target. On the other hand, perception of random-dot symmetry is still possible at isoluminance. The reason for this difference appears to be the need for exact-position information in movement but not symmetry perception. Control experiments suggest that the effects are not due to artefacts such as chromatic aberration in the eye.

Adult↗
PubMed1987

Detecting the displacements of spatial beats: a monocular capability.

Sensitivity to the sudden displacement (phase shift) of a single monocularly presented sinusoidal grating is increased when a static grating of similar spatial frequency is presented to the same eye. If the static grating is presented to the other eye instead sensitivity is, at best, halved. This demonstration implies that monocular and binocular visual pathways differ in their sensitivity to spatial variations of contrast. In addition it provides another example in which the monocular visual pathways are more sensitive to spatial displacements than the binocular pathways.

Depth Perception↗
PubMed1987

Spatial influences on colour opponent contributions to pattern detection.

The contribution of colour opponent mechanisms to detection thresholds is investigated at different spatial frequencies by presenting monochromatic, sinusoidal gratings on a uniform white background. Colour opponent mechanisms, characterised by a triple peaked spectral sensitivity function, determine threshold at low spatial frequencies (below 1 c/deg) and their contribution flattens the Weber function. They display low pass spatial frequency characteristics, becoming relatively more sensitive than non-opponent mechanisms as spatial frequency decreases. Colour opponent contributions are not revealed when the test grating and background are presented dichoptically.

Color Perception↗
PubMed1987

Stereoscopic contours and optokinetic nystagmus in normal and stereoblind subjects.

Moving stereoscopic contours in a dynamic random-dot stereogram have been previously shown to induce optokinetic nystagmus in subjects with normal stereopsis. For this to be validated as an objective test of stereopsis, stereoblind subjects must also be shown not to develop OKN, especially since it has been shown that the optomotor system of stereoblind individuals retains sensitivity to some cyclopean stimuli. In this report we verify that stereoblind subjects do not have an optomotor response to stereoscopic contours--regardless of the alignment angle at which the stereo image pair is presented.

Depth Perception↗
PubMed1988

Illusory contours induced by isoluminant chromatic patterns.

An illusory-contour was induced by abutting colored gratings embedded in the white field under isoluminance condition. The present study specified the stimulus conditions that invoked the just-perceptible illusory contours for the isoluminant chromatic patterns. The results showed that the purity difference between the colored lines and the white field required for the illusory-contour perception gave a function closely resembling in shape the function obtained for saturation discrimination. Increasing the width of lines reduced threshold for the perception of illusory contours, while the line spacing had no significant effect. The dependence of the illusory-contour perception upon saturation could be accounted for by considering the extraction of the edge and colour information by means of the opponent-color processes observed for the cells in the retina and LGN. On the other hand, the effects of the spatial parameters met the response properties observed for the cells in the visual cortex. It is suggested that the perception of illusory contour may result from hierarchical organization from the retina to cortex in the visual system.

Color Perception↗