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PubMed1993

Chromatic aberration and ocular focus: Fincham revisited.

Longitudinal chromatic aberration of the eye (LCA) produces "color fringes" at edges that specify focus. Fincham [(1951) British Journal of Ophthalmology, 35, 381-393] concluded that these chromatic effects were important for accommodation, but most investigators disagree. We monitored accommodation in 25 subjects while they viewed a sinusoidally moving target (1.5-2.5 D at 0.2 Hz) in a Badal optometer. The target was monochromatic (590 nm with 10 nm bandwidth), or white (3000 K) with LCA normal, neutralized or reversed. Sensitivity to the effects of LCA is profound and widespread. Gain decreases substantially and phase-lag increases when LCA is eliminated, and reversing the aberration severely disrupts accommodation. The ordered arrangement of spectral foci produced by LCA seems to be a fundamental aspect of the stimulus for "reflex" accommodation.

Accommodation, Ocular↗
PubMed1995

Human processing of colour information in the chromatic-frequency domain.

On the basis of MacAdam's data, we have computed a psychophysical function which characterizes the transference of the colour information processed by the human visual system in the chromatic frequency domain. This function, obtained using chromatic-discrimination criteria, shows a cut-off frequency between 0.01375 and 0.02 c/nm, depending upon the colour-tolerance units adopted.

Color Perception↗
PubMed1995

Nature of the pupillary responses evoked by chromatic flashes on a white background.

Color flashes on a steady-white background are classically used to isolate the response of the chromatic (color-opponent), as opposed to achromatic (luminance), channel in psychophysical investigations. The present study shows that pupillary responses evoked by such stimuli behave as if they are composed of functionally separable components. One component has a temporally transient waveform and has an action spectrum that is similar to the spectral sensitivity curve of the psychophysical chromatic channel. The present study discusses the possibility that the pupillary response is mediated by phasic (M-like) neurons and/or by tonic (P-like) neurons.

Color Perception↗
PubMed1994

Temporal integration at equiluminance and chromatic adaptation.

The present study showed that at equiluminance the critical duration of temporal integration became shorter as the chromatic saturation of an adaptation field was increased. These results suggest that the chromatic coding system (which is assumed to posses poorer temporal resolution or larger temporal integration time than the luminance coding system) can change its temporal integrating organization with its own adaptation level, independently of the luminance system.

Adaptation, Ocular↗
PubMed1994

Mechanisms of chromatic rod vision in scotopic illumination.

After viewing a coloured patch for 30 sec, successive contrast colours were triggered by stimulating either rods or cones. The conditions were arranged so that the rod and cone stimuli matched both with respect to chromaticness and brightness in a chromatically neutral state of adaptation. The results showed that the contrast colours triggered by rods were strikingly similar to those triggered by cones. Yet, the scotopic contrast colours, as compared with the photopic ones, were generally found to be somewhat displaced toward blue. This displacement was attributed to the difference in test conditions. Thus, it was suggested that, although rods may excite all the different types of spectrally opponent cells, they generally tend to prefer the short-wave cells. Moreover, it was concluded that the scotopic successive contrast colours are triggered by rod signals feeding into the primary rod pathway and therefore must originate centrally to the receptor level.

Color Perception↗
PubMed1994

The spatial tuning of chromatic mechanisms identified by simultaneous masking.

We have investigated the spatial transfer characteristics of the mechanisms sensitive to color in the human visual system using a method of simultaneous spatial masking with isoluminant chromatic stimuli. The test stimuli were Gaussian enveloped red-green gratings of three spatial frequencies in the lowpass region of the color domain (0.25, 0.5 and 1 c/deg). The masking stimuli were red-green gratings at the orientation and phase of the test, presented at the same spatial frequency, and at +/- 1, and +/- 2 octaves from its spatial frequency. We obtained test contrast threshold as a function of mask contrast for a wide range of mask contrasts (TvC functions). Tuning functions were derived from linear fits of the masking data, by taking the mask contrast that doubled the minimum test threshold at each spatial frequency. Chromatic tuning functions show bandpass characteristics for all test spatial frequencies examined with an average full bandwidth at half-height of 2.6 octaves, which is similar to the luminance bandwidths obtained under comparable conditions. Thus, our results suggest that the color contrast sensitivity function is the upper envelope of a range of bandpass mechanisms whose peaks extend to very low spatial frequencies.

Color Perception↗
PubMed1996

Perceived texture segregation in chromatic element-arrangement patterns: high intensity interference.

An element-arrangement pattern is composed of two types of elements that differ in the ways in which they are arranged in different regions of the pattern. We report experiments on the perceived segregation of chromatic element-arrangement patterns composed of equal-size red and blue squares as the luminances of the surround, the interspaces and the background (surround plus interspaces) are varied. Perceived segregation was markedly reduced by increasing the luminance of the interspaces. Perceived segregation was approximately constant for constant ratios of interspace luminance to square luminance and increased with the contrast ratio of the squares. Unlike achromatic element-arrangement patterns composed of squares differing in lightness [Beck et al (1991). Vision Research, 32, 719-743] perceived segregation did not decrease when the luminance of the interspaces was below that of the squares. Similar results were obtained for red and yellow, red and green, green and yellow, green and blue, and blue and yellow squares. Perceived segregation based on edge alignment was not interfered with by high intensity interspaces. Stereoscopic cues that caused the squares composing the element-arrangement pattern to be seen in front of the interspaces did not greatly improve perceived segregation. One explanation of the results is in terms of inhibitory interactions among achromatic and chromatic cortical cells tuned to spatial frequency and orientation. Alternately, the results may be explained in terms of how the luminance of the interspaces affects the grouping of the squares for encoding surface representations. Neither explanation accounts fully for the data and both mechanisms may be involved.

Color Perception↗
PubMed1996

Motion coherence across different chromatic axes.

It has been reported that equiluminant plaid patterns constructed from component gratings modulated along different axes of a cardinal colour space fail to create a coherent impression of two-dimensional motion [Krauskopf and Farell (1990). Nature, 348, 328-331]. In this paper we assess whether this lack of interaction between cardinal axes is a general finding or is instead dependent upon specific stimulus parameters. Type I and Type II plaids were made from sinusoidal components (1 cpd) each modulated along axes in a cardinal colour space and presented at equivalent perceived contrasts. The spatial angular difference between the two components was varied from 5 to 90 deg whilst keeping the Intersection of Constraints (I.O.C.) solution of the pattern constant. Observers were required to indicate the perceived direction of motion of the pattern in a single interval direction-identification task. We find that: (i) When plaids were made from components modulated along the same cardinal axis, coherent "pattern" motion was perceived at all angular differences. As the angular difference between the components decreased in a Type II plaid, the perceived direction of motion moved closer to the I.O.C. solution and away from that predicted by the vector sum. (ii) A plaid made from components modulated along red-green and blue-yellow cardinal axes (cross-cardinal axis) did not cohere at high angular differences (> 30 deg) but had a perceived direction of the fastest moving component. At lower angular differences, however, pattern motion was detected and approached the I.O.C. solution in much the same way as a same-cardinal axis Type II plaid. (iii) A plaid made from a luminance grating and a cardinal chromatic grating (red-green or blue-yellow) failed to cohere under all conditions, demonstrating that there is no interaction between luminance and chromatic cardinal axes. These results indicate that there are conditions under which red-green and blue-yellow cardinal components interact for the purposes of motion detection.

Color Perception↗
PubMed1996

Color appearance changes resulting from iso-luminant chromatic adaptation.

By means of asymmetric color matching, the effects of steady-state chromatic adaptation on the color appearance of briefly presented chromatic flashes were investigated. The adapting and test lights were of equal luminance (35 cd/m2) and differed from the standard grey adapting light either along the L-2M (red and green), or along the S-(L+M) (yellow and violet) line. The red (green) adapting light results in 6% positive (negative) L cone contrast and 11% negative (positive) M cone contrast with respect to the grey adapting light. The violet (yellowish) adapting light yields a positive (negative) S cone contrast of 50% relative to the standard adapting light. The main findings are: (i) iso-luminant adapting lights that differ only in their L-2M signal (red and green) resulted in asymmetric matches that differ mainly in the L-2M coordinate; (ii) iso-luminant adapting lights that differ in their S cone excitation only (yellow and violet) result in asymmetric matches that differ mainly in their S cone coordinate; (iii) the largest difference between test and match coordinates is found in the S cone signal for violet adaptation; (iv) the luminance differences of the asymmetric matches are within 1% of the mean luminance and are mostly non-systematic; (v) adaptation to iso-luminant red and green lights yields adaptational changes mainly in the L cones and not in the M cones; (vi) substantial quantitative deviations from a von Kries law are observed for L cone signals for red and green adaptation and for S cone decrements under yellow adaptation; (vii) S cone-isolating adapting lights results in small additive shifts in the S cone matches; adapting lights differing only in the L and M cone signal from the standard grey adapting light yield additive shifts only in the L and M cone matches.

Adaptation, Ocular↗
PubMed1988

Chromal focus of acquired chromatic discrimination loss and solvent exposure among printshop workers.

Acquired dyschromatopsia has been associated with exposure to organic solvents. However, the chromal focus of the loss may be indicative of its gravity. According to Kollner's rule, blue-yellow loss reflects changes in external retinal layers, while red-green loss appears to be indicative of internal retinal or optic nerve damage. The objective of the present study was to examine chromatic discrimination capacity of 30 printshop workers exposed to organic solvent mixtures, and of a non-exposed reference group. Colour vision was assessed with a colour arrangement test designed to detect acquired dyschromatopsia, the Lanthony D-15 desaturated panel. Quantitative analysis, using Bowman's colour confusion index, revealed significantly higher scores indicative of colour vision loss among the exposed workers as compared to the non-exposed. Analysis of covariance, with age as co-variate, showed colour confusion index to be significantly associated with job category. Similarly, qualitative analysis showed that the exposed workers presented a significantly higher prevalence of acquired dyschromatopsia as compared to the non-exposed group. However, analysis of the type of chromatic discrimination loss showed that among the nonexposed persons, dyschromatopsia was localized only in the blue-yellow range, while for 35% of the dyschromatopic-exposed persons, red-green loss as well as blue-yellow loss were present. Three-dimensional chi 2-analysis showed that the complex pattern of dyschromatopsia was not related to age, but to job category. These findings suggest that the type of dyschromatopsia, reflecting the gravity of neural alterations, may be a function of exposure level and/or the ophthalmotoxic properties of the particular solvents used.

Adult↗
PubMed2004

Visual completion of three-dimensional, chromatic, moving stimuli in humans.

We studied whether visual completion can be produced within three-dimensional (3-D), moving, chromatic objects. Rotating thin and thick discs with red sectors, forming the corners of Kanizsa triangle, were presented on a display. Observers also rotated a hand-held real thin Kanizsa triangle. An illusory, moving contour encompassing an illusory colourful triangle was generally observed. This indicates that the visual system is capable of filling in complex (3-D, moving, chromatic) percepts.

Adult↗
PubMed2004

The role of short-wavelength sensitive cones and chromatic aberration in the response to stationary and step accommodation stimuli.

The aim of the experiment was to test for a contribution from short-wavelength sensitive cones to the static and step accommodation response, to compare responses from short and long- plus middle-wavelength sensitive cone types, and to examine the contribution of a signal from longitudinal chromatic aberration to the accommodation response. Accommodation was monitored continuously (eight subjects) to a square-wave grating (2.2 c/d; 0.57 contrast) in a Badal optometer. The grating stepped (1.00 D) randomly towards or away from the eye from a starting position of 2.00 D. Five illumination conditions were used to isolate cone responses, and combine them with or without longitudinal chromatic aberration. Accuracy of the response before the step, step amplitude, latencies and time-constants, were compared between conditions using single factor ANOVA and t-test comparisons. Both S-cones and LM-cones mediated static and step accommodation responses. S-cone contrast drives "static" accommodation for near, but the S-cone response is too slow to influence step dynamics when LM-cones participate.

Accommodation, Ocular↗
PubMed2004

Modelling divergence in luminance and chromatic detection performance across measured divergence in surfperch (Embiotocidae) habitats.

This study predicts target detection performance in species-specific habitats for six surfperch (Embiotocidae) living in optically variable California kelp forests. Using species-specific measurements of habitat irradiance and photoreceptor absorbance in a simple dichromatic model for luminance and chromatic detection, the estimated performance of species' measured photopigments was compared to the theoretical maximum for each habitat. Modelling results suggest that changes in peak photoreceptor absorbance (lambda(max)), photoreceptor optical density, and photic environment may affect detection performance. Estimated performances for luminance detection were consistently high, while chromatic detection varied by habitat and demonstrated substantial improvements with increasing optical density differences between cone classes.

Adaptation, Ocular↗
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↗
PubMed2002

Interference of an apcA insertion with complementary chromatic adaptation in the diazotrophic Synechocystis sp. strain BO 8402.

Complementary chromatic adaptation was studied in two unicellular diazotrophic Synechocystis-type cyanobacteria, strains BO 8402 and BO 9201. Strain BO 8402 was isolated from Lake Constance as a mutant lacking phycobilisomes due to an insertion sequence element in the gene apcA, encoding alpha-allophycocyanin. Strain BO 9201 recovered the ability to assemble functional phycobilisomes after a spontaneous excision of the insertion sequence element in apcA. Simultaneously, the strain became able to perform group II complementary chromatic adaptation by regulating the synthesis of phycoerythrin. The two strains had identical phycoerythrin operons, cpeBA, and similar-sized transcripts were formed upon induction by green light. However, in strain BO 8402 the cpeBA transcript level was approx. 20-fold lower than in strain BO 9201. Because strain BO 8402 cannot synthesize allophycocyanin and phycocyanin is sequestered in paracrystalline inclusion bodies, non-assembled phycoerythrin may accumulate inside the cells. It was examined whether non-assembled phycoerythrin or other effects caused by the absence of phycobilisomes, such as a permanently oxidized redox status of the photosynthetic electron transport chain or a distorted ratio of C and N assimilation mediated the repression of cpeBA transcription in strain BO 8402. No such links could be established. We therefore concluded that in these diazotrophic Synechocystis-type cyanobacteria the green light-induced transcription of the cpe operon directly required a functional apc operon.

Bacterial Proteins↗
PubMed2001

Variation of chromatic sensitivity across the life span.

Thresholds were measured along three directions in color space for detecting an equiluminant color change of a set of bars embedded in a larger field of spatio-temporal achromatic noise for observers ranging in age from 3 months to 86 years. Pre-verbal observers were assessed with a forced-choice preferential-looking technique while older observers responded orally or manually. Over the life span, thresholds could be described along each color axis tested by a curve with two trends. Thresholds decreased with each doubling of age by nearly a factor of two until adolescence. Thereafter, thresholds increased by a factor of 1.4-2 with each doubling of age. Sensitivity to chromatic differences varied similarly along all three axes tested, suggesting uniformity in the sensitivity of chromatic mechanisms across the life span.

Adolescent↗
PubMed2001

Chromatic detection and discrimination analyzed by a Bayesian classifier.

Detection and threshold-level discrimination of Gabor patches were studied under the conditions of noise masking, in an attempt to isolate 'higher-order' or nonclassical color mechanisms. Detection contours in the equiluminant plane of cone contrast space were measured by varying test chromaticity in the presence of chromatic masking noise. Three equiluminant noise directions were used, in separate experiments. In the discrimination experiment, observers had to discriminate between pairs of stimuli that were fixed at their masked threshold contrasts. A Bayesian color classifier model was used to analyze the discrimination data, with no free parameters. There was no evidence of nonclassical color mechanisms in either the detection or discrimination data.

Bayes Theorem↗
PubMed1998

Development of the spatio-chromatic visual evoked potential (VEP): a longitudinal study.

Most prior visual evoked potential (VEP) research on the development of color vision has employed pattern-reversing stimuli that are not optimal for producing chromatic responses. We measured infant VEPs using low spatial frequency, onset-offset stimuli, modulated along the three axes of a cone-based color space (Derrington et al. [J. Physiol 1984;357, 241-265.]). Three color-normal infants were tested in a longitudinal design over the first postnatal year. One red/green color-deficient infant was also tested at 197 days. We found that VEP responses to S-axis (tritan) stimuli have their initial onset later than responses to red/green (L-M) or achromatic stimuli, and that developmental changes in VEP waveforms are more complex and longer lasting for chromatic than for achromatic stimuli. Possible mechanisms underlying these changes are discussed.

Adult↗