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At least 487 records · Page 27Linked to original sources
PubMed1997

Motion processing in pigeon tectum: equiluminant chromatic mechanisms.

Recent psychophysical and neurophysiological studies have suggested that, in mammals, there are interactions between the P (colour processing) and M (motion processing) visual pathways, which were previously believed to be parallel and separate. In this study, the role colour information plays in the coding of object motion was determined in the tectofugal pathway of pigeons. The responses of motion-sensitive neurons in the tectum to moving stimuli formed by chromatic contrast were recorded extracellularly using standard single-unit recording techniques. A moving coloured object was presented on a uniform (opponent coloured) background (e.g. blue-on-yellow, red-on-green and black-on-white). Through systematically manipulation of the luminance contrast between object and background, an equiluminant condition was generated. It was found that, at chromatic equiluminance, the majority of cells maintain some level of response. The mean magnitude of the response at equiluminance was about one-third of the response at maximal contrast to the same chromatic border. These results suggest that tectal units can detect motion of a pattern defined by a pure colour contour, although the strength of output is considerably weaker than that for the movement of patterns formed by luminance contrast.

Animals↗
PubMed2005

Loss of visual information in neglect: the effect of chromatic- versus luminance-contrast stimuli in a "what" task.

One to four vertical bars were tachistoscopically presented at various eccentricities along the horizontal meridian to patients with right brain damage and neglect (n=7) and to a control group of right brain damaged patients without neglect (n=4). Luminance contrast stimuli and isoluminant chromatic contrast stimuli were used. The patients' task was to report the number of bars. With luminance stimuli the neglect patients' discrimination in the left visual field was reduced, particularly at the most leftward position tested (ca 20 degrees ) where about 20% of the bars were omitted. The loss of information was limited to luminance contrast stimuli. When chromatic contrast stimuli were used, accuracy was comparable in the two hemifields and between groups of patients. The differential pattern of results for chromatic and luminance contrast stimuli is consistent with the hypothesis of a selective deficit of the magno-cellular pathway in neglect.

Aged↗
PubMed2005

Chromatic sensitivity of neurones in area MT of the anaesthetised macaque monkey compared to human motion perception.

We recorded activity from neurones in cortical motion-processing areas, middle temporal area (MT) and middle posterior superior temporal sulcus (MST), of anaesthetised and paralysed macaque monkeys in response to moving sinewave gratings modulated in luminance and chrominance. The activity of MT and MST neurones was highly dependent on luminance contrast. In three of four animals isoluminant chromatic modulations failed to activate MT/MST neurones significantly. At low luminance contrast a systematic dependence on chromaticity was revealed, attributable mostly to residual activity of the magnocellular pathway. Additionally, we found indications for a weak S-cone input, but rod intrusion could also have made a contribution. In contrast to the activity of MT and MST neurones, speed judgments and onset amplitude of evoked optokinetic eye movements in human subjects confronted with equivalent visual stimuli were largely independent of luminance modulation. Motion of every grating (including isoluminant) was readily visible for all but one observer. Similarity with the activity of MT/MST cells was found only for motion-nulling equivalent luminance contrast judgments at isoluminance. Our results suggest that areas MT and MST may not be involved in the processing of chromatic motion, but effects of central anaesthesia and/or the existence of intra- and inter-species differences must also be considered.

Adaptation, Physiological↗
PubMed1998

The effect of lesions to cortical areas V4 or AIT on pupillary responses to chromatic and achromatic stimuli in monkeys.

We measured the pupillary response to achromatic and chromatic grating stimuli in left and right visual hemifields of two rhesus monkeys, who were trained to fixate the centre of a screen. After removing the rostral inferior temporal cortex of one hemisphere, the response to chromatically modulated gratings in the contralateral hemifield was abolished, whereas the response to the luminance modulated grating was unaffected. In one of the monkeys, in which area V4 of the other hemisphere was also removed, there was no effect on the pupillary response to either kind of grating presented in the hemifield contralateral to the V4 lesion. The results show that the cortical contribution to the response of the pupil to purely chromatic changes is mediated by rostral temporal cortex, not by area V4.

Animals↗
PubMed2002

Discrimination of coloured patterns by honeybees through chromatic and achromatic cues.

We investigated pattern discrimination by worker honeybees, Apis mellifera, focusing on the roles of spectral cues and the angular size of patterns. Free-flying bees were trained to discriminate concentric patterns in a Y-maze. The rewarded pattern could be composed of either a cyan and a yellow colour, which presented both different chromatic and achromatic L-receptor contrast, or an orange and a blue colour, which presented different chromatic cues, but the same L-receptor contrast. The non-rewarded alternative was either a single-coloured disc with the colour of the central disc or the surrounding ring of the pattern, a checkerboard pattern with non-resolvable squares, the reversed pattern, or the elements of the training pattern (disc or ring alone). Bees resolved and learned both colour elements in the rewarded patterns and their spatial properties. When the patterns subtended large visual angles, this discrimination used chromatic cues only. Patterns with yellow or orange central discs were generalised toward the yellow and orange colours, respectively. When the patterns subtended a visual angle close to the detection limit and L-receptor contrast was mediating discrimination, pattern perception was reduced: bees perceived only the pattern element with higher contrast.

Animals↗
PubMed1986

Newborns' discrimination of chromatic from achromatic stimuli.

Two experiments assessed newborns' ability to discriminate chromatic from achromatic stimuli. In Experiment 1, newborns differentiated gray from green, from yellow, and from red: For each of these hues they preferred chromatic-and-gray checkerboards over gray squares matched in mean luminance, even though the luminance of the gray checks was varied systematically over a wide range so as to minimize nonchromatic cues. However, newborns showed no evidence of differentiating gray from blue: At some luminances they showed no preference for a blue-and-gray checkerboard over a gray square. In Experiment 2, newborns differentiated red from gray but appeared not to differentiate blue from gray: Following habituation to a series of gray squares of varying luminance, they looked longer at a red square than at a gray square of novel luminance but showed no such pattern of recovery to a blue square. The results imply that newborns have some, albeit limited, ability to discriminate chromatic from achromatic stimuli and hence, that they are at least dichromats.

Adult↗
PubMed1994

A novel noninvasive videographic method for quantifying changes in the chromaticity of the optic nerve head with changes in the intraocular pressure, pulsatile choroidal blood flow and visual neural function in humans.

Vision loss in glaucoma may be due to the compressive effects of the intraocular pressure (IOP) on the ganglion cell axons, impaired blood flow to the optic nerve, or some combination of these two factors. While reducing the IOP may preserve vision in patients with elevated IOP, not all patients experience longterm benefits from this therapeutic approach. The survival of ganglion cells may be more dependent upon the degree of vascular perfusion of the optic nerve head (ONH). In this report we present some preliminary data on a new noninvasive videographic technique for elaborating the capacity of the ONH vasculature to maintain perfusion constancy in the presence of transient elevations of the IOP and reductions of the ocular perfusion pressure (OPP). Shortterm, stepwise reductions of the OPP in the test eye of visually normal subjects (n = 5) systematically altered both the chromaticity (hue, saturation, brightness) of the ONH and the pulsatile ocular blood flow (POBF) in the choroid. Similar transient reductions in the OPP were seen to impair normal retinal physiology, as indicated by a significant attenuation of the bilateral pattern-reversal electroretinograms (pERGs) in visually normal subjects (n = 7). This technique was also used to reveal spontaneous rhythmical variations in the ONH chromaticity which were linked to the cardiac pulse rate. This so-called "chromatic pulse" of the ONH offers potential as a useful clinical index for evaluating the vascular perfusion of the ONH. The diagnostic and prognostic potential of dynamic digital imaging for the detection of abnormal hemodynamics in the ONH is discussed.

Blood Flow Velocity↗
PubMed1983

Longitudinal chromatic aberration of the vertebrate eye.

A recent study involving Abbe and Pulfrich refractometry analyses the dispersion of the human lens and the ocular media of a number of vertebrates. In general, the lens and, to a lesser extent, the cornea, are more dispersive than expected at wavelengths below 500 nm. The dispersion findings of this study were used in conjunction with reduced eye parameters of a number of vertebrates to calculate the longitudinal chromatic aberration of rock bass, frog, chicken, rat, cat, pig, cow, and human eyes. The calculated chromatic aberration of the human eye is greater than values reported earlier, because of the exaggerated dispersion of the lens at short wavelengths. While the values calculated for the additional species studies may be larger in some instances than expected, presumably due to lens dispersion as well, chromatic aberration is not large enough to account for the hyperopia found by retinoscopic study of small eyes.

Animals↗
PubMed1984

Threshold temporal integration of chromatic stimuli.

We measured colorimetric purity thresholds as a function of stimulus duration for seven wavelengths between 430 and 650 nm. Purity thresholds were measured in a hue substitution mode. The purity-duration function showed decreasing purity as duration was increased to about 640 msec. Functions for different wavelengths could be fit by a fixed chromatic template displaced on the purity axis. Increment thresholds as a function of duration were measured for white and chromatic lights added to a homogeneous white stimulus field. The "white" function showed no integration beyond 160 msec and was fit by an achromatic template. The wavelength functions were not parallel; wavelengths at the spectral extremes showed longer integration times, similar to the purity-duration functions. Increment data could be fit by a vector sum of chromatic and achromatic templates.

Color Perception↗
PubMed1985

Two temporal phases, brightness-dependent and -independent, in the chromatic response elicited by a briefly-flashed monochromatic light: a preliminary report.

The strength of chromatic response elicited by a briefly-flashed monochromatic light, which varied in its exposure duration, was measured with the "transient cancellation method" in Experiment 1. It was found that the chromatic response of a test color depended on brightness of the test field, up to the exposures of 100-200 msec. But it began to decrease, independent of brightness of the field, at the longer durations. The above results were confirmed by Experiment 2, in which the perceived saturation of a colored light was estimated with the two alternative forced choice method. Those results were tentatively interpreted as indicating the two kinds of chromatic responses presumably originating at the different stages in the visual system. Some other psychophysical dada on color vision were briefly referred to in relation to the present results.

Color Perception↗
PubMed1986

Visual evoked potentials to luminance and chromatic contrast in rhesus monkeys.

The spatial and temporal tuning of the luminance and chromatic systems were investigated using visual evoked potentials (VEPs) recorded from rhesus monkeys. VEPs were recorded from eight bipolar electrodes which were chronically implanted in the foveal projection region of area 17 in two monkeys. They were elicited by luminance (yellow-black) and chromatic (red-green) since-wave gratings which varied in spatial frequency (1, 4, 8 and 12 c/deg) and temporal frequency (3, 6, 10 and 15 Hz). The findings showed that chromatic VEPs exhibit low-pass tuning in both the spatial and temporal domains, whereas luminance VEPs exhibit bandpass tuning in the spatial domain and low-pass tuning in the temporal domain. The spatial tuning findings are consistent with the psychophysical literature, while the low-pass temporal tuning shown by the luminance VEPs was attributed to various cancellations and distortions in the suprathreshold VEP at high flicker rates and to the effects of the anesthesia.

Animals↗
PubMed1986

Stimuli for accommodation: blur, chromatic aberration and size.

We investigated the frequency response of the accommodative system (0.05-1 Hz) using three stimuli: defocus blur, the effects of the chromatic aberration of the eye, and changing target size. A high-speed infrared optometer monitored accommodation while the subject viewed a target in a Badal optometer. Blur was provided by moving the target sinusoidally towards and away from the subject (1-3 D) and the size of the target was varied at the same frequency. Chromatic aberration was controlled by using either monochromatic (590 nm) or white light (3300 K). Gain and phase plots changed systematically as we varied the number of stimuli presented together. This suggests that besides defocus blur both chromatic aberration and changing size are involved in accommodative control.

Accommodation, Ocular↗
PubMed1989

Response pooling between chromatic and luminance systems.

Two experiments were designed to examine interactions of the responses of the chromatic and luminance systems to suprathreshold stimuli. We measured simple reaction times (RT) to eight photometrically matched (1 cd/m2) wavelengths between 448 and 658 nm. These chromatic test stimuli were incrementally presented on either a spatially coextensive 1.2 or a larger 2 degrees steady white background. Sectors of the outer annulus region (between 1.2 and 2 degrees) could be removed to allow systematic variation of the extent of the spatial contour between test and background fields. When the white background was spatially coincident with the test field, RTs showed trichromatic saturation-like wavelength dependence, with a maximum RT at 572 nm. As white sectors were added to the annulus (introducing spatial transients between test and background fields), RTs became less and less wavelength-dependent, and were nearly wavelength-independent when a full annulus was used. The data were analysed in terms of a two-system RT model for processing chromaticity and luminance.

Color Perception↗
PubMed1990

The optical transverse chromatic aberration on the fovea of the human eye.

The horizontal component of optical transverse chromatic aberration (TCA) at the fovea between 486 and 656 nm is measured in a sample of 8 eyes by two novel methods, both using vernier adjustment tasks with a retinal illumination of approx. 780 td and for a pupil size of approximately 5.5 mm dia. Initially, in an indirect method, TCA is derived along the line of sight from chromatic parallax. Secondly, TCA is measured directly using a semi-Maxwellian view and compensating for longitudinal chromatic aberration (LCA). Both techniques are unaffected by coma or by the Stiles-Crawford effects, thus optical TCA rather than the TCA perceived in normal view is measured. On average, optical TCA is in the same direction but less than previously predicted by eye models and predictions of the optical quality of the eye in white light are modified. Factors underlying the lower average value of optical TCA and variability among subjects, especially pupil centration and foveal position, are discussed. The relationship of optical TCA to TCA perceived in normal view and to chromostereopsis is analysed. The results suggest that the optical design of the human eye is optimized to reduce the wavelength dependent phase shift in the optical transfer function, which could be produced by optical TCA.

Accommodation, Ocular↗
PubMed1990

"Colour constancy" in Mondrian patterns: a partial cancellation of physical chromaticity shifts by simultaneous contrast.

Edwin Land's Mondrian demonstrations (Land 1977, 1983, 1986a) are striking examples that the perceived colours of objects are largely independent of the chromaticity of the light incident upon them. Attempts to implement this independence in artificial vision systems have renewed interest in colour constancy and contrast, and the explanation of these phenomena in the Retinex theory. We use colour matches to demonstrate that departures from "colour constancy" are large and that it is possible to obtain the same colour shifts when the complex Mondrian pattern is replaced by a homogeneous grey field surrounding a test patch. A given patch has the same colour when surrounded by the Mondrian as when set in a grey background, provided that the grey represents the spatially weighted average of the Mondrian. Neither the colour shifts nor the equivalence of this neutral surround are correctly predicted by the Retinex theory. The phenomenon of partial cancellation of physical chromaticity shifts with changes of illuminant thus reduces to one of simultaneous contrast and adaptation where a spatio-chromatic and luminance average over a Mondrian pattern is the same as for a grey surround. Experiments with simultaneous contrast demonstrate that spatial weighting factors need to be applied in computations of the effect of the separate areas of a complex Mondrian pattern.

Algorithms↗
PubMed1991

Vernier acuity: effects of chromatic content, blur and contrast.

Offset thresholds were measured for targets whose horizontal profiles were either Gaussian or odd-symmetric Gabor functions. The targets were defined either by variation along the constant B or the constant R & G axes of color space or by luminance variation. Blur was varied in the case of the Gaussian targets by varying the standard deviation of the distribution and in the case of the Gabor functions by varying the spatial frequency of the sinusoidal component. Detection thresholds for all the stimuli were measured. The contrast of the targets used in the measurement of offset thresholds was varied from just above detection threshold to the maximum that could be produced. The offset thresholds obtained with targets of different chromatic composition are nearly identical when blur and contrast relative to detection threshold are held constant. We attribute the slight advantage held by luminance targets over chromatic targets for narrow Gaussians to the detectability of low frequency components of the chromatic targets which are of little use in the assessment of offsets. This conjecture is supported by the complete absence of such an advantage in the case of Gabor targets.

Color Perception↗
PubMed1991

Interocular differences in transverse chromatic aberration determine chromostereopsis for small pupils.

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.

Color Perception↗
PubMed1991

Detection of chromatic deviations from white across the human visual field.

We studied how much blue, green, or red light had to be added to or subtracted from white to obtain veridical hue perception (blue, green, red, or their complementary colours) at various locations in the temporal visual field. The CIE 1931 (x, y) chromaticity coordinates corresponding to a veridical hue perception were subtracted from the chromaticity coordinates of the white (0.35, 0.35) in order to obtain the threshold differences (dx, dy) in chromaticity coordinates. When stimulus size was constant at all visual field locations, dx and dy changed with eccentricity. However, when the stimulus was M-scaled by magnifying its size with increasing eccentricity in inverse proportion to the lowest local sampling density across the human retina (cones and ganglion cells at eccentricities 0-10 and above 10 deg, respectively), dx and dy remained constant at all eccentricities.

Adult↗