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PubMed2005

Associating color appearance with the cone chromaticity space.

A cone chromaticity space, a transform of a colorimetric specification system into coordinates that represent cone excitations, does not provide color appearance information. Boynton and Olson (Color Research and Application 12, 94-105, 1987) gathered color naming for the 424 Optical Society of America Uniform Color Scales (OSA-UCS) color samples. Here, a computational algorithm was developed that converts OSA-UCS sample values into L, M, S cone excitations based on the 1964 CIE 10 degrees Standard Observer. This makes it possible to plot the cone chromaticities associated with the eight color names used by Boynton and Olsen's observers to describe the non-dark appearing colors.

Algorithms↗
PubMed2006

Illusory color mixing upon perceptual fading and filling-in does not result in 'forbidden colors'.

A retinally stabilized object readily undergoes perceptual fading. It is commonly believed that the color of the apparently vanished object is filled in with the color of the background because the features of the filled-in area are determined by features located outside the stabilized boundary. Crane, H. D., & Piantanida, T. P. (1983) (On seeing reddish green and yellowish blue. Science, 221, 1078-1080) reported that the colors that are perceived upon full or partial perceptual fading can be 'forbidden' in the sense that they violate color opponency theory. For example, they claimed that their subjects could perceive "reddish greens" and "yellowish blues." Here we use visual stimuli composed of spatially alternating stripes of two different colors to investigate the characteristics of color mixing during perceptual filling-in, and to determine whether 'forbidden colors' really occur. Our results show that (1) the filled-in color is not solely determined by the background color, but can be the mixture of the background and the foreground color; (2) apparent color mixing can occur even when the two colors are presented to different eyes, implying that color mixing during filling-in is in part a cortical phenomenon; and (3) perceived colors are not 'forbidden colors' at all, but rather intermediate colors.

Adult↗
PubMed2006

Almost complete colour constancy achieved with full-field adaptation.

A successive asymmetric colour-matching task was used to study the changes in colour appearance of simulated Munsell samples. Colour shifts were induced with two Planckian illuminants, standard illuminant A (u'=0.256, v'=0.524) and illuminant S (u'=0.174, v'=0.392). Measurements were conducted with a 20 degrees field and a 120 degrees field. Adaptation period varied from 1 to 30s with the smaller field and from 1 to 60s with the larger field. Colour shifts were specified in terms of a modified Brunswik ratio (BR). Higher values of BR were associated with longer adaptation periods but only when the larger background was used. Supplementary experiments showed that the changes in colour appearance were related to a slight shift in the perceived colour of the background. The timing of the colour shifts are modelled in terms of cone opponent responses. High values of BR correspond to almost complete von Kries adaptation in all three cone types.

Adaptation, Ocular↗
PubMed2006

The role of perceptual learning on modality-specific visual attentional effects.

Morrone et al. [Morrone, M. C., Denti, V., & Spinelli, D. (2002). Color and luminance contrasts attract independent attention. Current Biology, 12, 1134-1137] reported that the detrimental effect on contrast discrimination thresholds of performing a concomitant task is modality specific: performing a secondary luminance task has no effect on colour contrast thresholds, and vice versa. Here we confirm this result with a novel task involving learning of spatial position, and go on to show that it is not specific to the cardinal colour axes: secondary tasks with red-green stimuli impede performance on a blue-yellow task and vice versa. We further show that the attentional effect can be abolished with continued training over 2-4 training days (2-20 training sessions), and that the effect of learning is transferable to new target positions. Given the finding of transference, we discuss the possibility that V4 is a site of plasticity for both stimulus types, and that the separation is due to a luminance-colour separation within this cortical area.

Attention↗
PubMed2003

Macular dystrophy in a Japanese family with fundus albipunctatus.

PURPOSE: To report a Japanese family with fundus albipunctatus and macular dystrophy associated with a mutation in the 11-cis retinol dehydrogenase (RDH5) gene. DESIGN: Observational case report. METHOD: Ophthalmic examinations and DNA analysis were performed. RESULTS: The fundi of a 56-year-old man and his 51-year-old sister showed numerous yellow-white punctata. He also had bull's-eye maculopathy and prepappillary arterial loops, whereas she did not, and his best-corrected visual acuity was impaired, whereas hers was normal. Their kinetic visual fields did, however, show central or paracentral scotoma, and both had tritanomalous color vision. Their scotopic electroretinograms were typical of fundus albipunctatus, and photopic electroretinograms were significantly reduced. A homozygous Gly107Arg mutation in the RDH5 gene was detected in both siblings. CONCLUSIONS: We suggest that the macular dystrophy is caused by the RDH5 gene mutation as a phenotype variation in fundus albipunctatus.

Alcohol Oxidoreductases↗
PubMed1983

Pupillary defects in amblyopia.

We examined the pupils of 55 amblyopic subjects to determine whether a pupillary defect could be detected in the amblyopic eye. We found relative afferent pupillary defects in 45 of the subjects; these defects were equal to or larger than 0.3 log unit (that is, easily visible) in 29 subjects. The pupillary defect was always in the amblyopic eye, but it could not be correlated with the severity or the cause of the amblyopia, with visual-evoked potential abnormalities, or with color vision defects.

Adolescent↗
PubMed1980

Atrophic maculopathy associated with hereditary ataxia.

Two siblings had atrophic maculopathy associated with hereditary ataxia clinically defined as an olivopontocerebellar degeneration. The macular changes were suggestive of an early bull's-eye maculopathy in one case and of a late atrophic stage of bull's-eye maculopathy in the other. This suggests that concentric annular (bull's-eye) macular dystrophy may occur as part of olivopontocerebellomacular degeneration. Exogenous causes were excluded. The inheritance pattern was autosomal recessive or irregular autosomal dominant. The relationship of these two degenerative disorders is not yet clear. This combination of findings has been, to our knowledge, only rarely described.

Adolescent↗
PubMed1981

Visual function abnormalities in macular heterotopia caused by proliferative diabetic retinopathy.

In seven patients with displacement of the macula in one eye caused by vitreoretinal traction from proliferative diabetic retinopathy, the macula was displaced toward the optic disk in all but one eye. The eyes with macular heterotopia showed (1) reduced visual acuity (ranging from 6/6 (20/20) to 6/24 (20/80), (2) reduced static perimetry sensitivity (particularly in the temporal field) with displacement of the peak sensitivity toward the blind spot, (3) loss of hue discrimination, and (4) metamorphopsia. In two eyes with macular heterotopia, Stiles-Crawford data provided evidence for photoreceptor disorientation; one eye had mixed orientation, and the other a displaced peak suggesting regular photoreceptor tilting. The proposed mechanisms of visual loss in eyes with macular heterotopia secondary to traction from proliferative diabetic retinopathy include detachment of the macula, disorientation of photoreceptors in the macula, and disturbance of normal neural connections within the retina caused by stretching of the retina.

Adult↗
PubMed2000

Opponent-color models and the influence of rod signals on the loci of unique hues.

To investigate how rod signals influence hue perception and how this influence can be incorporated into opponent-color models, we measured the shift of unique-hue loci under dark-adapted conditions compared with cone-plateau conditions. Rod signals produced shifts of all spectral unique hues (blue, green, yellow) but in a pattern that was inconsistent with simple additive combinations of rod and cone inputs in opponent-color models. The shifts are consistent with non-linear models in which rod influence requires non-zero cone signals. Cone-signal strength may modulate or gate rod influence, or rod signals may change the gain of cone pathways.

Adaptation, Ocular↗
PubMed2003

Chromatic induction and the layout of colours within a complex scene.

A target's apparent colour is influenced by the colours in its surrounding. If the surrounding consists of a single coloured surface, the influence is a shift 'away' from the surface's colour. If the surface is more than 1 degrees from the target area the shift is very small. If there are many surfaces, then not only the average luminance and chromaticity of the surfaces matters, but also the chromatic variability. It is not yet clear whether it makes any difference where the chromatic variability is within the scene, so we constructed stimuli in which the chromatic variability was restricted to certain regions. We found that it made very little difference where the chromatic variability was located. The extent to which the average colour of nearby surfaces influences the apparent colour of the target seems to depend on the average chromatic variability of the whole scene.

Color Perception↗
PubMed2003

Color and motion: which is the tortoise and which is the hare?

Recent psychophysical studies have been interpreted to indicate that the perception of motion temporally either lags or is synchronous with the perception of color. These results appear to be at odds with neurophysiological data, which show that the average response-onset latency is shorter in the cortical areas responsible for motion (e.g., MT and MST) than for color processing (e.g., V4). The purpose of this study was to compare the perceptual asynchrony between motion and color on two psychophysical tasks. In the color correspondence task, observers indicated the predominant color of an 18 degrees x 18 degrees field of colored dots when they moved in a specific direction. On each trial, the dots periodically changed color from red to green and moved cyclically at 15, 30 or 60 deg/s in two directions separated by 180 degrees, 135 degrees, 90 degrees or 45 degrees. In the temporal order judgment task, observers indicated whether a change in color occurred before or after a change in motion, within a single cycle of the moving-dot stimulus. In the color correspondence task, we found that the perceptual asynchrony between color and motion depends on the difference in directions within the motion cycle, but does not depend on the dot velocity. In the temporal order judgment task, the perceptual asynchrony is substantially shorter than for the color correspondence task, and does not depend on the change in motion direction or the dot velocity. These findings suggest that it is inappropriate to interpret previous psychophysical results as evidence that motion perception generally lags color perception. We discuss our data in the context of a "two-stage sustained-transient" functional model for the processing of various perceptual attributes.

Analysis of Variance↗
PubMed1998

Dependence of color on context in a case of cortical color vision deficiency.

Color constancy depends on sensitivity to change in both illumination spectral properties and object position. We investigated this latter form of color constancy by asking a cerebral achromatopsic to name the colors of papers that were presented atop black, gray or white backgrounds under identical illumination. Comparison of color names across background conditions reveals poor constancy, characterized by a contrasting of foreground and background values that is not corrected by proper anchoring.

Brain Diseases↗
PubMed1998

Shift in Rayleigh matches after adaptation to monochromatic light of various intensities.

The action spectrum for inducing a long-lasting protan shift in colour matches was investigated. Rayleigh matches were measured before and after 30 min adaptation to monochromatic light of 520, 550, 580 or 620 nm. For each wavelength, seven retinal illuminances, ranging from 3.0 to 5.0 log td, were chosen in random order. Results for one colour-normal observer show that the shift in Rayleigh match after adaptation increases monotonically as a function of the luminance of the adapting light. The dynamic response range is from 3.3 to 4.7 log td. The wavelength of the adapting light had no systematic influence on the form of the response function. The results imply that the effect is triggered by light absorbed in the photopigments themselves.

Adaptation, Ocular↗
PubMed1998

Recent evolution of uniform trichromacy in a New World monkey.

Until recently, New World primates were found to have a single M/L photopigment gene on the X-chromosome. This arrangement limits males to dichromatic, or monochromatic color vision. Only females who were heterozygous for the M/L gene were trichromatic. Recently, an exception has been discovered. Male howler monkeys appear to have more than one M/L pigment gene, and both genders are uniformly trichromatic. We characterized promoter regions corresponding to two M/L pigment genes in howlers. Comparison of DNA sequences with those of humans and three species of New World primate suggest a recent and independent acquisition of a second M/L gene locus in the howler.

Animals↗