Internal spatial relationships in young children's drawings.
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Contrast sensitivity for sinusoidal gratings of different spatial frequencies and low spatial frequency discrimination of high contrast squarewave gratings were measured in 26 right brain damaged patients, 15 of whom showed symptoms of spatial hemi-neglect. No difference was present between neglect and non-neglect patients in either task. A difference in contrast sensitivity restricted to low spatial frequencies was present between controls and patients, independent of neglect. Overall, results indicated that spatial vision at threshold and suprathreshold levels is not selectively impaired in patients with hemi-neglect, a finding consistent with theories which postulate a post-perceptual locus of impairment in this syndrome.
It has been proposed that the functions of the two major parallel channels of the primate visual system, the color-opponent and the broad-band, can be determined in psychophysical experiments by eliminating luminance but maintaining chrominance information (isoluminance), since under such conditions the broad-band channel is believed to be silenced. To test this proposition we examined the visual functions of monkeys after blocking either of these channels and we also assessed the responses of neurons to isoluminant stimuli in the lateral geniculate nucleus. We show that color, texture, stereopsis and pattern perception in the absence of the color-opponent channel, and flicker and motion perception in the absence of the broad-band channel are compromised. Yet isoluminance functions for stereopsis and texture in the absence of the broad-band channel and for motion in the absence of the color-opponent channel are indistinguishable from normal. Our recordings show that the neuronal responses of the broad-band cells for isoluminant exchange of red and green lights are reduced but not eliminated and that the color-opponent cells also become similarly less responsive under these conditions. We conclude that perceptual losses at isoluminance are not specific for either channel.
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Grating acuity, interocular suppression and binocular interaction were evaluated at different positions in the visual field of strabismic humans with alternating fixation. In all cases, the suppression of the deviated eye was most intense in a region corresponding to the fovea of the fixating eye, but reduced or absent in the periphery. In addition, suppression was found in part of the peripheral visual field of the fixating eye. For most subjects, the monocular properties of both eyes were normal. However, for one subject with a strong preference for one of the eyes, visual acuity and luminance detection were selectively impaired in the chronically suppressed regions of the non-preferred eye. Regardless of which eye was currently used for fixation, the visual information available to the subject came from both eyes. In parts of the visual field, the two eyes tended to replace each other. In the far periphery, and especially in the upper and lower hemifield, signals from the two eyes were often combined in a binocular perception of depth.
Although previous research has shown that depth perception is weak for isoluminant stereograms, the possibility remains that color plays an important role in stereopsis when luminance variations are present. To examine this possibility, we measured the relative contribution of chromatic and luminance cues in solving the correspondence problem for ambiguous "wallpaper" stereograms composed of vertical bars. Using an ideal-observer analysis, we found that chromatic cues were used much more efficiently than luminance cues in disambiguating these stereograms when the patterns were presented on a dark background but were used with about equal efficiency when presented on a light background. Another experiment (using the same wallpaper patterns) showed that chromatic and luminance cues were also used with about equal efficiency in a standard stereo detection task. Some of the implications of these results for theories of stereo vision are discussed.
Chromostereopsis has been attributed previously to interocular differences in foveal transverse chromatic aberration (TCA). We tested this hypothesis by measuring chromostereopsis as a function of the separation of small artificial pupils. We also measured the monocular transverse chromatic aberration under the same conditions. Our results show that chromostereopsis with small pupils can be precisely accounted for by the interocular difference in monocular transverse chromatic aberration. This relationship is closely predicted by a simple water eye model.
A color CRT image display system was used to present adapting backgrounds that were spatially and temporally varied. Three observers adjusted the chromaticity of test stimuli to produce an achromatic appearance under a variety of adapting conditions. The achromatic-appearing chromaticities were used as measures of the observers' states of chromatic adaptation. The spatial configuration of the adapting background was varied to measure the spatial extent of the mechanisms responsible for chromatic adaptation. The temporal configuration of the adapting background was varied to measure the time-course of these mechanisms. The results show that chromatic adaptation is spatially localized with a time-course on the order of 10 sec. Since the mechanisms were shown to be spatially localized, the observed temporal integration across eye movements is required to allow these mechanisms to adjust to the spatially integrated scene chromaticity.
Several studies have reported that the magnitude of chromostereopsis changes as the pupil size changes. Einthoven's theory, that chromostereopsis is determined by interocular differences of monocular transverse chromatic aberration, can not easily explain this change. Therefore, several alternative hypotheses have been introduced, most notably by Vos [(1960) Vision Research, 6, 105-107], who argues that shifts in chromostereopsis with pupil size are due to decentration of the peak of the Stiles-Crawford effect (SCE) with respect to the pupil. We tested this hypothesis by measuring chromostereopsis under both scotopic (no SCE) and photopic conditions with centered and decentered artificial pupils. The results show that the SCE plays an important role in the effect of pupil size on chromostereopsis. Similar changes were also measured in monocular chromatic diplopia which supports the hypothesis that the effect of pupil size on chromostereopsis is due to monocular mechanisms.
Visual illusions and ambiguous figures are difficult to perceive when presented in a manner which stimulates only chromatic pathways. This perceptual limitation could indicate that these pathways are unable to mediate form perception, or it may reflect the relative visibility of the stimulus, regardless of the pathway utilized. To examine this issue, an ambiguous figure (illusory Necker cube) was presented to the short wavelength sensitive (S) cone pathway which is thought to convey only chromatic signals. Although few observers could recognize the cube when presented in isolation to S cones, the same reduction in recognition was found when the cube was detected by achromatic pathways at a level of visibility comparable to that conveyed by S cones. Our results indicate that for this object recognition task, visibility of the stimulus is the relevant variable, rather than the particular pathway traversed. Prior experience was also found to be important determinant of object recognition.
Dynamic random dot fusion, stereopsis and stereoacuity were evaluated in 149 healthy, fullterm infants, using both forced-choice preferential looking (FPL) and steady-state visual evoked potential (VEP) protocols. Few infants aged 2-3 months demonstrated fusion or stereopsis in either the FPL or VEP protocol; most infants aged 5 months and older demonstrated fusion and stereopsis in both protocols. Both FLP and VEP stereoacuity approached adult-level (< 60 sec) by 6-7 months of age. Both infants and adults exhibited non-monotonic VEP amplitude vs disparity functions with a step change in phase at an intermediate disparity, consistent with separate fine and coarse disparity mechanisms.