Chromatic Contrast Sensitivity Research Articles

The Chromatic and Achromatic Contrast Sensitivity Function in the Far Periphery

The Chromatic and Achromatic Contrast Sensitivity Function in the Far Periphery

ColorVideoVDP: A visual difference predictor for image, video and display distortions

ColorVideoVDP is a video and image quality metric that models spatial and temporal aspects of vision for both luminance and color. The metric is built on novel psychophysical models of chromatic spatiotemporal contrast sensitivity and cross-channel contrast masking. It accounts for the viewing conditions, geometric, and photometric characteristics of the display. It was trained to predict common video-streaming distortions (e.g., video compression, rescaling, and transmission errors) and also 8 new distortion types related to AR/VR displays (e.g., light source and waveguide non-uniformities). To address the latter application, we collected our novel XR-Display-Artifact-Video quality dataset (XR-DAVID), comprised of 336 distorted videos. Extensive testing on XR-DAVID, as well as several datasets from the literature, indicate a significant gain in prediction performance compared to existing metrics. ColorVideoVDP opens the doors to many novel applications that require the joint automated spatiotemporal assessment of luminance and color distortions, including video streaming, display specification, and design, visual comparison of results, and perceptually-guided quality optimization. The code for the metric can be found at https://github.com/gfxdisp/ColorVideoVDP.

Visual function and retinal thickness in children with type 1 diabetes mellitus

ABSTRACT Clinical Relevance The possibility that changes in blue–yellow visual thresholds and some retinal thickness measures in children with diabetes mellitus may be observed before any visible fundus changes points to the possibility of these measures being a useful predictor that the risks of diabetic retinopathy are higher in some children than in others. Introduction Previous studies showed mixed results on chromatic and achromatic contrast sensitivity early in the course of diabetes mellitus, and the findings of these studies may have been influenced by a lack of experimental sensitivity to visual deficits, a bias towards tritan-like errors or the cognitive demands of the tests and variations in sample composition. The purpose of this study was to evaluate colour and contrast thresholds and retinal thickness in children with type 1 diabetes mellitus compared with age-matched controls. Methods A prospective case–control study was carried out on 9–14-year-old children with type 1 diabetes mellitus (49 cases) and age matched controls (49) in which isoluminant red–green and blue–yellow and achromatic luminance contrast thresholds were measured. Fundus photography was used to grade diabetic retinopathy. Retinal thickness parameters were measured using optical coherence tomography. Data on the duration of diabetes mellitus, glycaemic control (HbA1c), blood glucose level, body mass index, blood pressure and blood oxygenation at the time of testing were obtained. Results The cases mostly had poorly controlled diabetes, HbA1c 8.6% (6.4–12.8%), for an average (range) duration of 5 (0.4–12) years. The cases had significantly higher blue–yellow thresholds (p = 0.02) and greater total retinal and inner retinal thickness (p < 0.05) than controls. No cases had diabetic retinopathy. Within the cases, poorer visual function and systemic health measures were associated with thinner retinal structures and greater global loss volume percentage in the ganglion cell complex. Conclusion Blue–yellow thresholds of cases were raised compared to normal. Within the cases, higher luminance contrast thresholds were also associated with, mostly, ganglion cell complex reductions.

Riemannian color difference metric for spatial sinusoidal color variations

Several studies report on the sensitivity of human vision to static spatial sinusoidal achromatic and chromatic contrast variations. However, a Riemannian color difference metric, which includes the spatial and colorimetric properties of sinusoidal gratings, is lacking. Such a metric is important for various applications. Here we report on the development of a new Riemannian metric, for the prediction of detection ellipsoids in color space, for spatial sinusoidal gratings as a function of the grating’s size, spatial frequency, luminance and chromaticity. The metric is based on measurements and models of achromatic and isoluminous chromatic contrast sensitivity functions available in literature, and the Riemannian metric for split fields which we reported earlier. We find adequate agreement with various data sets of experimental achromatic and isoluminous chromatic contrast sensitivity functions and with experimentally determined threshold ellipses of isoluminous chromatic Gabor gratings.

Applying Resampling and Visualization Methods in Factor Analysis to Model Human Spatial Vision.

Studies have reported different numbers of spatial frequency channels for chromatic and achromatic vision. To resolve the difference, we performed factor analysis, a multivariate modeling technique, on population data of achromatic and chromatic sensitivity. In addition, we included resampling and visualization methods to evaluate models from factor analysis. These routines are complex but widely useful. Therefore we have archived our analysis routines by building smCSF, an open-source software package in R (https://smin95.github.io/dataviz/). Data of 103 normally-sighted adults were analyzed. They included blue-yellow, red-green, and achromatic contrast sensitivity. To obtain the confidence interval of relevant statistical parameters, factor analysis was performed using a resampling method. Then exploratory models were developed. We then performed model selections by fitting them against the empirical data and quantifying the quality of the fits. During the exploratory factor analysis, different statistical tests supported different factor models. These could partially be reasons for why there have been conflicting reports. However, after the confirmatory analysis, we found that a model that included two spatial channels was adequate to approximate the chromatic sensitivity data, whereas that with three channels was so for the achromatic sensitivity data. Our findings provide novel insights about the spatial channels for chromatic and achromatic contrast sensitivity from population data. Also, the analysis and visualization routines have been archived in a computational package to boost the transparency and replicability of science.

Poster Session I: Diurnal variations in luminance and chromatic contrast sensitivity.

Sensory motor performance typically peaks in the evening, influenced by observer's diurnal arousal level. The arousal level is regulated by neurons in the brainstem, which form connections extending throughout the brain but the connection is highly heterogeneous. The dorsal visual pathway and superior colliculus receive a dense projections, while the ventral visual pathway and lateral geniculate nucleus receive fewer. The former primarily deal with stimuli determined by luminance contrast, while the latter handle chromatic information. How such heterogeneous projection in the brain impacts on human visual detection performance has yet to be understood. In this study, we measured the diurnal variation in human contrast sensitivity and investigated whether changes differed between luminance and chromatic stimuli. Result revealed that as the time of day progressed, sensitivity to luminance contrast improved, while sensitivity to color contrast deteriorated.

Melanopsin enhances image persistence

Contributions of the inner retinal photopigment melanopsin to human visual perception are incompletely understood. Here, we use a four-primary display to produce stimuli differing in melanopsin versus cone contrast in psychophysical paradigms in eight subjects with normal color vision. We address two predictions from electrophysiological recordings of the melanopsin system in non-human mammals: melanopsin influences color and/or supports image persistence under visual fixation. We first construct chromatic contrast sensitivity contours for stimuli differing in melanopsin excitation presented as a central annulus (10°) or peripheral (22.5°) spot. We find that although including melanopsin contrast produces modest changes in the average chromatic coordinates in both eccentricities, this occurs equally at low (0.5Hz) and higher (3.75Hz) temporal frequencies, arguing that it reflects divergence in cone spectral sensitivity in our participants from that captured in standardized cone fundamentals rather than a melanopsin contribution to color. We continue to ask whether the established ability of melanopsin to sustain firing of visual neurons under extended light exposure has a visual correlate, using the optical illusion of Troxler fading in which blurred spots in periphery disappear during visual fixation. We find that introducing additional melanopsin contrast (+28% Michelson contrast) to either bright or dark spots increases fading latency by 35%± 8.8% and 41%± 13.6%, respectively. Our data argue that the primary contribution of melanopsin to perception under these conditions isnot to provide a color percept but rather to enhance persistence of low spatial frequency patterns during visual fixation.

A Study of Spatial Chromatic Contrast Sensitivity based on Different Colors, Luminance, and Stimulus Patterns

A Study of Spatial Chromatic Contrast Sensitivity based on Different Colors, Luminance, and Stimulus Patterns

Achromatic and chromatic contrast discrimination in patients with type 2 diabetes

Effects of type 2 diabetes on achromatic and chromatic contrast sensitivity (CS) are still controversial. In this study, we aimed to investigate CS in patients without diabetic retinopathy (no-DR) and in those with non-proliferative DR (NPDR) and proliferative DR (PDR) using psychophysical methods with transient and sustained achromatic stimuli and color patches. Achromatic CS was measured with the pulsed pedestal (PP) paradigm (7, 12, and 19 cd/m2) and pedestal-△-pedestal (P-△-P) paradigm (11.4, 18, and 28.5 cd/m2). A chromatic discrimination paradigm that assesses protan, deutan, and tritan color vision was adopted. Forty-two patients (no-DR n = 24, NPDR n = 12, PDR = 6; male n = 22, mean age = 58.1 y/o) and 38 controls (male n = 18, mean age = 53.4 y/o) participated. In patients, mean thresholds were higher than in controls and linear trends were significant in most conditions. For the PP paradigm, differences were significant in the PDR and NPDR groups in the 7 and 12 cd/m2 condition. For the P-△-P paradigm, differences were only significant in the PDR group in the 11 cd/m2 condition. Chromatic contrast loss was significant in the PDR group along the protan, deutan and tritan axes. The results suggest independent involvements of achromatic and chromatic CS in diabetic patients.

Continuous motion tracking to rapidly estimate chromatic contrast sensitivity and identify color deficiency

Continuous motion tracking to rapidly estimate chromatic contrast sensitivity and identify color deficiency

A Study of Spatial Chromatic Contrast Sensitivity based on Different Colour Background

The goals of this work are to accumulate the experimental data on contrast sensitivity functions and to establish a visual model that incorporates spatial frequency dependence. In addition, the experimental results from fixed-size and fixed-cycles stimuli and from different luminance levels were compared. Such a model is highly desired for applications that rely on image quality and to serve the lighting and imaging industries. The detection thresholds have been measured for chromatic contrast patterns at different spatial frequencies. The experimental parameters included: (1) four colour centres (white, green, yellow, and red), which were recommended by the International Commission on Illumination (CIE), at two different luminance levels for each colour centre; (2) three colour directions for each colour centre, namely luminance, red-green and yellow-blue; (3) five spatial frequencies, 0.06, 0.24, 0.96, 3.84, and 6.00 cycles per degree (cpd) for fixed-cycles stimulation, in which two spatial frequencies, 0.24 and 6.00 cpd, were also chosen for fixed-size stimuli. In this experiment, a 10-bit display characterized by GOG model was used to obtain contrast thresholds of different colour centres by 2-alternative forced choice method and stair-case method. The experimental results revealed different parameter effects (colour centres, luminance, colour direction, fixed cycle/size), and also supported McCann's conclusion that the number of cycles affects the comparative sensitivity. Most importantly, a cone contrast model was successfully developed by fitting the visual test data (fixed number of cycles). The model could accurately predict the contrast sensitivity of different color centers, spatial frequencies and stimulus.

Selective deficits of S-cone in thyroid-associated ophthalmopathy patients without clinical signs of dysthyroid optic neuropathy.

PurposeWe explored whether thyroid-associated ophthalmopathy (TAO) patients without clinical signs of dysthyroid optic neuropathy (DON) would have a selective deficit mediated by S-cone.MethodsThirty-two TAO patients without clinical signs of DON (non-DON, 42.03 ± 9.59 years old) and 27 healthy controls (41.46 ± 6.72 years old) participated in this prospective, cross-sectional study. All observers were tested psychophysically after passing color screening tests and a comprehensive ocular examination. Isolated L-, M-, and S-cone contrast thresholds were measured at 0.5 cyc/deg using Gabor patches. We calculated the area under the receiver operating characteristic (ROC) curve to quantify the ability of chromatic contrast sensitivity to detect the early visual function changes in non-DON patients.ResultsS-cone contrast sensitivity in non-DON patients was found to be lower than that of healthy controls (P < 0.001), whereas the sensitivities to L- and M-cone Gabor patches were similar between these two groups (P = 0.297, 0.666, respectively). Our analysis of the ROC curve revealed that the sensitivity to S-cone had the highest index to discriminate non-DON patients from healthy controls (AUC = 0.846, P < 0.001). The deficit of S-cone was significantly correlated with muscle index in non-DON patients (R = 0.576, P = 0.001).ConclusionThere is a selective S-cone deficit in the early stage of TAO. S-cone contrast sensitivity could serve as a sensitive measure of visual impairments associated with early DON in patients with TAO.

Chromatic Contrast Sensitivity Functions and Colour Discrimination in Smoker Patients.

In this study, effects of smoking on colour vision with the Farnsworth–Munsell 100 Hue test (FM100h) and achromatic (A), red-green (RG), and blue-yellow (BY) contrast sensitivity functions were evaluated. In total, 50 non-smoker controls and 25 smokers, divided into two groups (group 1, less than 10 cigarettes per day, with 15 patients, and group 2, >10 cigarettes per day, with 10 patients) took part in the experiments. Best-corrected visual acuity (BCVA), FM100h, and A, RG, and BY contrast sensitivity functions were measured. Total and partial RG and BY error scores (TES and PTES) and colour axis index (CA) were used in the analysis. No differences between smoker and non-smoker groups were found in BCVA, CA and A and BY contrast sensitivity, but TES and PTES values and RG contrast sensitivity at 1 cpd were statistically different. Differences between smoker groups were not significant. Error scores in smokers were positively correlated with the number of cigarettes smoked per day, and in BY also with age. Tobacco caused discrimination losses in both chromatic mechanisms but affected the red-green pathway more than the blue-yellow, and therefore, a partial RG score of FM100h test seems to be a good predictor of smoker colour deficiencies.

Short-Term Peripheral Contrast Reduction Affects Central Chromatic and Achromatic Contrast Sensitivity

Peripheral retinal contrast reduction is suggested as a potential myopia control strategy. However, the underlying mechanism is yet unknown. Therefore, this study investigated the influence of peripheral contrast reduction on central chromatic and achromatic contrast sensitivity (CS). A total of 19 participants were included. Peripheral contrast reduction was induced via Bangerter foils of 0.4 and 0.8 density, each with a clear central zone of 8.0 mm diameter. Central achromatic and chromatic (for S-, M-, and L-cone types) CS was measured at 3 and 12 cpd in a 2-IFC psychophysical procedure. CS was tested monocularly at 0, 30, and 90 min of adaptation time, while the fellow eye was covered by an infrared filter. With the filter in place, pupil size was controlled to be smaller than the clear central aperture. Data were analyzed using linear mixed models. Cone-type CS showed significant differences among each other (all p &lt; 0.05), except for the achromatic and L-cone type (p = 0.87). The minimum sensitivity was found with the S-cone type and the maximum with the M-cone type. Central achromatic and chromatic CS were equally affected by diffusion. The level of peripheral diffusion also influenced CS, while the 0.8 Bangerter foil led to a higher reduction in CS compared to the 0.4 Bangerter foil (p = 0.0008) and the control condition (p = 0.05). A significant reduction in CS occurred between 30 and 90 min of adaptation time (p &lt; 0.0001). The current study found that peripheral contrast reduction impacted central achromatic and chromatic CS equally. It further showed that the amplitude of reduction was influenced by the level of diffusion, with the reduction becoming more pronounced over time.

Influence of Stimulus Size on Simultaneous Chromatic Induction.

Chromatic induction is a major contextual effect of color appearance. Patterned backgrounds are known to induce strong chromatic induction effects. However, it has not been clarified whether the spatial extent of the chromatic surrounding induces a chromatic contrast or assimilation effects. In this study, we examined the influence of the width of a center line and its flanking white contour on the color appearance when the line was surrounded by chromatic backgrounds. A strong color shift was observed when the center line was flanked by white contours with the L/M- and S-cone chromatic backgrounds. There was a difference between the optimal widths of the center line and the contour for the shift in color appearance for the L/M-cone chromaticity (0.9 and 1.1–1.7 min, respectively) and the S-cone chromaticity (8.2–17.5 and 0.9–2.5 min, respectively). The optimal width of the center line for the L/M-cone was finer than the resolution-limit width of the chromatic contrast sensitivity and coarser than that of the luminance contrast sensitivity. Thus, the color appearance of the center line could be obtained by integrating broad chromatic information and fine luminance details. Due to blurring and chromatic aberrations, the simulated artifact was large for the darker center line and S-cone background, thus suggesting that the artifact could explain the luminance dependency of the induction along the S-cone chromaticity. Moreover, the findings of this study reveal that the dominant factor of the color shift is neural instead of optical.

Modeling chromatic contrast sensitivity across different background colors and luminance

In this research we compare chromatic contrast sensitivity models for two separate datasets and for the pooled dataset. They were obtained from two studies employing a very similar experimental paradigm. The data represent threshold visibilities of chromatic Gabor patterns varying in spatial frequency, background chromaticity, direction of color modulation and luminance, at constant stimulus size. Using the extended data set, we reconfirm our previously reported finding that a model based on coloropponent contrast signals is an improvement over a cone contrast model. However, when linear background scaling in classic cone contrast is replaced by nonlinear background scaling, an improvement of almost similar size is obtained. The results of this study can be of interest for the development of vision models employing the processing of spatio-chromatic information.

Temporal filtering of luminance and chromaticity in macaque visual cortex

SummaryContrast sensitivity peaks near 10 Hz for luminance modulations and at lower frequencies for modulations between equiluminant lights. This difference is rooted in retinal filtering, but additional filtering occurs in the cerebral cortex. To measure the cortical contributions to luminance and chromatic temporal contrast sensitivity, signals in the lateral geniculate nucleus (LGN) were compared to the behavioral contrast sensitivity of macaque monkeys. Long wavelength-sensitive (L) and medium wavelength-sensitive (M) cones were modulated in phase to produce a luminance modulation (L + M) or in counterphase to produce a chromatic modulation (L − M). The sensitivity of LGN neurons was well matched to behavioral sensitivity at low temporal frequencies but was approximately 7 times greater at high temporal frequencies. Similar results were obtained for L + M and L − M modulations. These results show that differences in the shapes of the luminance and chromatic temporal contrast sensitivity functions are due almost entirely to pre-cortical mechanisms.

Visual function deficits in eyes with resolved endophthalmitis

To evaluate the changes in functional vision in patients with resolved endophthalmitis. This was a cross-sectional study. The study included 20 patients with resolved endophthalmitis and best-corrected visual acuity of 20/100 or better. Visual acuity (VA), contrast threshold (CT), red/green (RG) and yellow/blue (YB) colour vision and 15 Hz flicker modulation threshold (FMT) were assessed using standard psychophysical techniques. The median age was 54 years. The median visual acuity was 0.27 (~ 20/40—Snellen Equivalent) ((interquartile range [IQR]), 0.30) logMAR). The median log contrast threshold (CT) was − 1.13 (IQR, 0.36) log units (normative value for age-matched CT: − 1.61 log units). The median red/green (RG) and yellow/blue (YB) thresholds were 11.52 (IQR, 26.19) and 9.45 (IQR, 16.20) CAD units respectively, which were at least 5 times higher than age-matched normative RG and YB thresholds. The median central cone- mediated FMT was 17.64% (IQR, 23.40%), which was much higher compared to age-matched FMT (5.48% [IQR, 3.47]). Linear regression revealed significant relationship between contrast thresholds and foveal thickness (y = 0.001x−1.47, R2 = 0.20, p = 0.048). Though endophthalmitis may resolve with a good visual acuity, deficits in visual functions like chromatic discrimination, cone-mediated flicker and contrast sensitivity persist.

Spatio-chromatic contrast sensitivity across the lifespan: interactions between age and light level in high dynamic range

We investigated spatio-chromatic contrast sensitivity in both younger and older color-normal observers. We tested how the adapting light level affected the contrast sensitivity and whether there was a differential age-related change in sensitivity. Contrast sensitivity was measured along three directions in colour space (achromatic, red-green, yellowish-violet), at background luminance levels from 0.02 to 2000 cd/m2, and different stimuli sizes using 4AFC method on a high dynamic range display. 20 observers with a mean age of 33 y. o. a. and 20 older observers with mean age of 65 participated in the study. Within each session, observers were fully adapted to the fixed background luminance. Our main findings are: (1) Contrast sensitivity increases with background luminance up to around 200 cd/m2, then either declines in case of achromatic contrast sensitivity, or remains constant in case of chromatic contrast sensitivity; (2) The sensitivity of the younger age group is higher than that for the older age group by 0.3 log units on average. Only for the achromatic contrast sensitivity, the old age group shows a relatively larger decline in sensitivity for medium to high spatial frequencies at high photopic light levels; (3) Peak frequency, peak sensitivity and cut-off frequency of contrast sensitivity functions show decreasing trends with age and the rate of this decrease is dependent on mean luminance. The data is being modeled to predict contrast sensitivity as a function of age, luminance level, spatial frequency, and stimulus size.

Are Spatial Chromatic Contrast Sensitivity Band-pass or Lowpass Functions?

The goal of this research is to generate high quality chromatic Contrast Sensitivity Function (CSF) over a wide range of spatial frequencies from 0.06 to 3.84 cycles per degree (cpd) surrounding 5 CIE proposed colour centres (white, red, yellow, green and blue) to study colour difference. At each centre, 6 colour directions at each of 7 frequencies were sampled, from 0.06 to 3.84 cycles per degree (cpd) corresponding to the number of cycles: from 2.3 to 144.4 respectively. A threshold method based on forced-choice stair-case was adopted to investigate the just noticeable (threshold) colour difference. The results revealed that the chromatic CSF under the present experimental conditions having many lower spatial frequencies covering five colour centres to be band pass, whereas previous results indicated it was low pass. However, this could be caused by the present experimental conditions such as fixed-size stimuli and constant luminance. The new chromatic CSF for R-G and Y-B channels were also developed.