Melanopsin-driven surround induction on the red/green balance of yellow.

To test the potential role of melanopsin-dependent ipRGCs in surround induction effects, we used a four-channel projector apparatus to hold the cone activity in a surround constant while varying the amount of melanopsin activity between two levels: low (baseline) and high (136% of the baseline). Rods were partially controlled by having the subjects complete conditions after either adapting to a bright field or darkness. The subjects adjusted the red/green balance of a 2.5° central target that varied in its ratio of L and M cones, but was equiluminant with the surround, to a perceptual null point (neither reddish nor greenish). When the surround melanopsin activity was higher, the subjects set their yellow balances at significantly higher L/(L+M) ratios, suggesting the high melanopsin surround was inducing greenishness into the central yellow stimulus. This is consistent with surround brightness effects that show the induction of greenishness into a central yellow test by high luminance surrounds. This potentially provides further evidence for a general role of melanopsin activity in brightness perception.

Word and color impressions measured with normal and simulated deutan color stimulus sets in color vision normal and deuteranopic observers.

Impressions of nine semantic words expressing abstract meanings were measured by a color selection process using twelve hues from vivid tone in the Practical Color Coordinate System (PCCS) as well as White, Grey and Black (as a normal color stimulus set) in a paired comparison method (Experiment 1). Color impressions were rated using 35 paired words in a semantic differential (SD) method (Experiment 2). The data of ten color vision normal (CVN) and four deuteranopic observers were analyzed separately by principal component analysis (PCA). Our previous study [J. Opt. Soc. Am. A37, A181 (2020)JOAOD60740-323210.1364/JOSAA.382518] using these methods indicated that deuteranopes could understand the impression of all colors if the color names can be recognized, even if deuteranopes cannot perceive redness and greenness. In this study, we also used a simulated deutan color stimulus set in which colors were modified to simulate the color appearance in deuteranopes by using Brettel-Viénot-Mollon's model to investigate how these simulated deutan colors would be treated by the deutan observers. In the CVN and deutan observers, color distributions of the principal component (PC) loading values in Experiment 1 were close to the PCCS hue circle in the normal colors, and those of the simulated deutan colors could be fitted by ellipses, but there were wide gaps of 73.7° (CVNs) and 89.5° (deutan) where only "White" existed. The word distributions as the PC score values could also be fitted by ellipses and are moderately similar between stimulus sets, but the fitting ellipses were considerably compressed in the minor axis directions in the deutan observers, although categories of words were similar between observer groups. The word distributions in Experiment 2 were not statistically different between the observer groups and the stimulus sets. The color distribution of the PC score values were statistically different, but tendencies of the color distributions were similar between observers. The color distributions of the normal colors could be fitted by ellipses, similar to the hue circle, and those of the simulated deutan colors could be fitted by cubic function curves. These results suggest that both of the stimulus sets were perceived as one dimensional and as a monotonic series of colors by a deuteranope, but the deuteranope can recognize the difference of the stimulus sets and recall the color distributions of each set, similar to those in the CVN observers.

Perception of brown with variation in center chromaticity and surround luminance.

Brown is a contrast color that depends on complex combinations of chromatic and achromatic signals. We measured brown perception with variations in chromaticity and luminance in center-surround configurations. In Experiment 1, the dominant wavelength and saturation in terms of S-cone stimulation were tested with five observers in a fixed surround luminance (60c d/m 2). A paired-comparison task required the observer to select the better exemplar of brown in one of two, simultaneously presented, stimuli (1.0° center diameter; annulus of 9.48° outer-diameter). In Experiment 2, the same task was tested with five observers in which surround luminance was varied (from 13.1 to 99.6c d/m 2) for two center chromaticities. The results were a set of win-loss ratios for each stimulus combination and converted to Z-scores. An ANOVA did not reveal a significant main effect of the observer factor but revealed a significant interaction with red/green (a ∗) [but not with the dominant wavelength and the S-cone stimulation (or b ∗)]. Experiment 2 revealed observer variation in interactions with surround luminance and S-cone stimulation. The averaged data plotted in 1976 L ∗ a ∗ b ∗ color space indicate that high Z-score values widely distribute in the area of a ∗ from 5 to 28 and b ∗ over 6. The balance of the strength between yellowness and blackness differs among observers owing to the amount of induced blackness required for the best brown.

Uncertainty drives exploration of negative information across younger and older adults.

Although individuals generally avoid negative information, recent research documents that they voluntarily explore negative information to resolve uncertainty. However, it remains unclear (a) whether uncertainty facilitates exploration similarly when exploration is expected to lead to negative, neutral, or positive information, and (b) whether older adults seek negative information to reduce uncertainty like younger adults do. This study addresses the two issues across four experimental studies (N = 407). The results indicate that individuals are more likely to expose themselves to negative information when uncertainty is high. In contrast, when information was expected to be neutral or positive, the uncertainty surrounding it did not significantly alter individuals' exploration behavior. Furthermore, we found that uncertainty increased the exploration of negative information in both older and younger adults. In addition, both younger and older adults chose to explore negative information to reduce uncertainty, even when there were positive or neutral alternatives. In contrast to the age-related similarities in these behavioral measures, older adults demonstrated reduced scores in questionnaires on sensation seeking and curiosity, relative to their counterparts who were younger. These results suggest that information uncertainty has a selective facilitation effect on exploration for negative information and that normal aging does not alter this tendency, despite age-related reductions in self-reported measures of personality traits relevant to information seeking.

Robust categorical color constancy along daylight locus in red-green color deficiency.

Categorical color constancy in normal trichromats has been found to be very robust in real scenes. In this study, we investigated categorical color constancy in red-green dichromats and anomalous trichromats. Eight dichromats (two protanopes and six deuteranopes), eight anomalous trichromats (four protanomalous and four deuteranomalous trichromats), and eight normal trichromats sorted 208 Munsell matte surfaces into Berlin and Kay's basic color categories under D65 illuminant, F illuminant with correlated color temperature 4200 K, and TL84 illuminant with correlated color temperature 2700 K. Color constancy was quantified by a color constancy index. The results showed that the constancy index of dichromats (0.79) was considerable and significantly lower than that of normal trichromats (0.87) while that of anomalous trichromats (0.84) was not. The impairment of color constancy performance in dichromats was expected to be caused by their large intra-subject variabilities in color naming. The results indicate robust categorical color constancy along daylight locus in red-green dichromats and anomalous trichromats, which might be contributed by cone adaptation mechanism and be independent of color discrimination mechanism. It suggests that the color categorization by color vision deficient subjects can be reasonable without any assistants of artificial equipment in daily life under sunlight and common illuminations.

Aging of visual mechanisms.

Optical and neural changes in the aging human visual system are reviewed in terms of factors that can influence the study of light-mediated effects on circadian physiology. All aspects of early stage visual mechanisms change continuously from the first days of life, and these changes must be understood when investigating both conscious and unconscious visual responses to light throughout the life span.

Interactive modulations between congruency sequence effects and validity sequence effects.

Sequential modulations have been found in both conflict and spatial orienting tasks. The former is called congruency sequence effects (CSE) and the latter is called validity sequence effects (VSE). Although the two effects have similar phenomenon descriptions, the relationship of the cognitive control mechanisms under the two effects is still unclear. Using a modified attentional network test (ANT), a flanker task and an arrow cueing task are integrated into a single task, which enables the test of the possible interactions between CSE and VSE. Since a confound-minimized design is used, the observed sequence effects cannot be attributed to the feature integration of low-level stimulus features or the contingency learning. It was found that the CSE are only significant when the arrow cue in preceding trial is invalid, and the VSE are only significant when the target letter in preceding trial is congruent with the distractor letters. The findings suggest that the sequential modulations during orienting and executive control of attention networks are highly interacted with each other, and the sequence effects in these networks are possibly controlled by a complex and multifaceted adaptive control mechanism.

Suppression of Luminance Contrast Sensitivity by Weak Color Presentation.

The results of psychophysical studies suggest that color in a visual scene affects luminance contrast perception. In our brain imaging studies we have found evidence of an effect of chromatic information on luminance information. The dependency of saturation on brain activity in the visual cortices was measured by functional magnetic resonance imaging (fMRI) while the subjects were observing visual stimuli consisting of colored patches of various hues manipulated in saturation (Chroma value in the Munsell color system) on an achromatic background. The results indicate that the patches suppressed luminance driven brain activity. Furthermore, the suppression was stronger rather than weaker for patches with lower saturation colors, although suppression was absent when gray patches were presented instead of colored patches. We also measured brain activity while the subjects observed only the patches (on a uniformly black background) and confirmed that the colored patches alone did not give rise to differences in brain activity for different Chroma values. The chromatic information affects the luminance information in V1, since the effect was observed in early visual cortices (V2 and V3) and the ventral pathway (hV4), as well as in the dorsal pathway (V3A/B). In addition, we conducted a psychophysical experiment in which the ability to discriminate luminance contrast on a grating was measured. Discrimination was worse when weak (less saturated) colored patches were attached to the grating than when strong (saturated) colored patches or achromatic patches were attached. The results of both the fMRI and psychophysical experiments were consistent in that the effects of color were greater in the conditions with low saturation colors.

Relative contributions of melanopsin to brightness discrimination when hue and luminance also vary.

A large number of studies have shown the effect of melanopsin-dependent retinal ganglion cells on humans performing brightness discrimination tasks. These studies often utilized targets that only differ in their melanopsin activation levels, and not in their luminance or hue, which are both factors that make large contributions to brightness discrimination. The purpose of the present study was to evaluate the relative contribution of melanopsin activation to brightness discrimination when luminance and hue are also varying in addition to melanopsin activation. Using an apparatus consisting of three separate high luminance projectors, we were able to manipulate melanopsin-isolating stimulation, and L-, M-, and S-cone stimulation separately, thus allowing us to vary stimuli in their melanopsin activation, luminance, and hue category independently. We constructed three sets of target stimuli with three different levels of melanopsin activation (100%, 131%, and 167% relative melanopsin excitation) and five levels of luminance. We then had subjects do a two-alternative forced choice task where they compared the previously described target stimuli set to a set of four comparison stimuli that varied in their hue category but had identical luminances. We found that in our stimuli set the overall contribution of melanopsin activity to brightness discrimination was small (an average of 6% increase in likelihood to call a high melanopsin activity stimulus brighter compared to a low melanopsin activity stimulus) when luminance and hue also varied. However, a significant interaction showed that when the comparison was between stimuli differing only in melanopsin stimulation (with luminance and hue unchanged) the contribution of melanopsin to brightness judgments was about 3 times larger (an average of 18% increase in likelihood to call a high melanopsin activity stimulus brighter compared to a low melanopsin activity stimulus). This suggests that although luminance and hue have large effects on brightness discrimination such that the melanopsin contribution can become hard to detect, when there are minimal cone-dependent signals available, melanopsin can make a large contribution to brightness discrimination.

Bidirectional relationships between semantic words and hues in color vision normal and deuteranopic observers.

We previously showed that impressions of nine semantic words expressing abstract meanings (like "tranquil") can be expressed by 12 hues in a paired comparison method; in this study, White, Gray, and Black were added (Exp. 1) to the previous 12 hues. Color impressions were also estimated using a set of 35 paired words by a semantic differential (SD) method (Exp. 2). The data of nine color vision normal (CVN) and seven color vision deficient (CVD) observers (one protanope and six deuteranopes) were analyzed separately by principal component analysis (PCA). In the results of Exp. 1, all hues used as loadings were distributed in a hue-circle shape in the 2D color space of PC axes for both observer groups [however, the four bluish hues (Blue-Green to Violet) tended toward convergence]. One data set of five CVNs and five deuteranopes was analyzed together using PCA because of high concordance. In the word distribution of the CVDs in Exp. 1, because second PC scores tended to be smaller, the categorization of the words was not clear; the points of five word scores were approximately on one line, reflecting that the colors used in the paired comparison were treated in one-dimensional scaling (which correlates to lightness) in the CVDs. In the results of Exp. 2, the word distribution of loadings was similar between the CVNs and CVDs, and the color score distribution had a similar tendency of showing an ellipse-shaped hue circle; it was probably caused by their experience of being associated with color names rather than color appearance (although the radius of the short axis is shorter in the CVDs' data). The comparison of the word distribution between experiments suggests that two to five semantic word impressions can be stably expressed by hue, but the impression of other words, such as "Magnificent" for the CVNs and "Fine" for the CVDs, cannot. The hue circle is conceptually kept in the SD measurement for all observers; however, it was not kept in the paired comparison for the CVDs. The analysis of one combined data set suggests that the 2D color distribution is not caused by a 3D color system because the lightness scaling is involved in the 2D color distribution.

Semantic word impressions expressed by hue.

We investigated the possibility of whether impressions of semantic words showing complex concepts could be stably expressed by hues. Using a paired comparison method, we asked ten subjects to select from a pair of hues the one that more suitably matched a word impression. We employed nine Japanese semantic words and used twelve hues from vivid tones in the practical color coordinate system. As examples of the results, for the word "vigorous" the most frequently selected color was yellow and the least selected was blue to purple; for "tranquil" the most selected was yellow to green and the least selected was red. Principal component analysis of the selection data indicated that the cumulative contribution rate of the first two components was 94.6%, and in the two-dimensional space of the components, all hues were distributed as a hue-circle shape. In addition, comparison with additional data of color impressions measured by a semantic differential method suggested that most semantic word impressions can be stably expressed by hue, but the impression of some words, such as "magnificent" cannot. These results suggest that semantic word impression can be expressed reasonably well by color, and that hues are treated as impressions from the hue circle, not from color categories.

Age-related changes in ON and OFF responses to luminance increments and decrements.

Impulse response functions for an incremental luminous pulse (ON flash) or a decremental luminous pulse (OFF flash) were derived for twelve young (19-24 years old) and ten old (65-84 years old) observers. Thresholds were measured for two pulses separated by stimulus-onset-asynchronies from 13.3 to 186.7 ms. The pulses had a spatial Gaussian shape and were presented as increments or decrements on a 15 cd/m2 equal-energy white background, having the same chromaticity as the pulse. A spatial four-alternative forced-choice method was combined with a staircase procedure. Retinal illuminance was equated individually by heterochromatic flicker photometry and using a 2.3-mm exit pupil in a Maxwellian-view optical system to reduce the effects of age-related changes and individual variations in lens density and pupil size. Luminance ON- and OFF-impulse response functions calculated from the threshold data revealed significant age-related changes in the response amplitude of both first excitatory and first inhibitory phases. However, there were no significant changes in the time to the first peak or the second peak. These age-related changes in luminance varying ON- and OFF-impulse response functions (IRFs), reflecting putative properties of the magnocellular pathway, are discussed in relation to motion detection and the balance of ON and OFF pathways across the life span.

Possible influences on color constancy by motion of color targets and by attention-controlled gaze.

We investigated the influence of motion on color constancy using a chromatic stimulus presented in various conditions (static, motion, and rotation). Attention to the stimulus and background was also controlled in different gaze modes, constant fixation of the stimulus, and random viewing of the stimulus. Color constancy was examined in six young observers using a haploscopic view of a computer monitor. The target and background were illuminated in simulation by red, green, blue, and yellow, shifted from daylight (D65) by specific color differences along L - M or S - (L + M) axes on the equiluminance plane. The standard pattern (under D65) and test pattern (under the color illuminant) of a 5-deg square were presented side by side, consisting of 1.2-deg square targets with one of 12 colors at each center, surrounded by 230 background ellipses consisting of eight other colors. The central color targets in both patterns flipped between top and bottom locations at the rate of 3 deg/s in the motion condition. The results indicated an average reduction of color constancy over the 12 test colors by motion. The random viewing parameter indicated better color constancy by more attention to the background, although the difference was not significant. Color constancy of the four color illuminations was better to worse in green, red, yellow, and blue, respectively. The reduction of color constancy by motion could be explained by less contribution of the illumination estimation effect on color constancy. In the motion with constant fixation condition, the retina strongly adapted to the mean chromaticity of the background. However, motion resulted in less attention to the color of the background, causing a weaker effect of the illumination estimation. Conversely, in the static state with a random viewing condition, more attention to the background colors caused a stronger illumination estimation effect, and color constancy was improved overall.

Sequence effects of the involuntary and the voluntary components of symbolic cueing.

The orienting of attention has been found to be influenced by the previous cueing status in a spatial-cueing paradigm. The explanation for this sequence effect remains uncertain. This study separated the involuntary and the voluntary components of arrow cueing by manipulating the predicted target locations. For example, a left arrow cue may have indicated that the target was more likely to appear at the up location. Therefore, three trial types were repeated or switched between trials: cued (targets appeared along the direction of the arrows), predicted (targets appeared at the locations predicted by the arrows), and unrelated (targets appeared at the other two locations, neither cued nor predicted). RTs of cued trials were found to be significantly facilitated after a previous cued trial; however, the same effect was not observed for predicted trials. The results suggest that significant sequence effects are induced only in the involuntary component of arrow cueing. The findings support the feature-integration hypothesis for the sequence effect of symbolic cueing.

Color constancy of color-deficient observers under illuminations defined by individual color discrimination ellipsoids.

We explored the color constancy mechanisms of color-deficient observers under red, green, blue, and yellow illuminations. The red and green illuminations were defined individually by the longer axis of the color discrimination ellipsoid measured by the Cambridge Colour Test. Four dichromats (3 protanopes and 1 deuteranope), two anomalous trichromats (2 deuteranomalous observers), and five color-normal observers were asked to complete the color constancy task by making a simultaneous paper match under asymmetrical illuminations in haploscopic view on a monitor. The von Kries adaptation model was applied to estimate the cone responses. The model fits showed that for all color-deficient observers under all illuminations, the adjustment of the S-cone response or blue-yellow chromatically opponent responses modeled with the simple assumption of cone deletion in a certain type (S-M, S-L or S-(L+M)) was consistent with the principle of the von Kries model. The degree of adaptation was similar to that of color-normal observers. The results indicate that the color constancy of color-deficient observers is mediated by the simplified blue-yellow color system with a von Kries-type adaptation effect, even in the case of brightness match, as well as by a possible cone-level adaptation to the S-cone when the illumination produces a strong S-cone stimulation, such as blue illumination.

Discrimination thresholds of normal and anomalous trichromats: Model of senescent changes in ocular media density on the Cambridge Colour Test.

Age-related changes in chromatic discrimination along dichromatic confusion lines were measured with the Cambridge Colour Test (CCT). One hundred and sixty-two individuals (16 to 88 years old) with normal Rayleigh matches were the major focus of this paper. An additional 32 anomalous trichromats classified by their Rayleigh matches were also tested. All subjects were screened to rule out abnormalities of the anterior and posterior segments. Thresholds on all three chromatic vectors measured with the CCT showed age-related increases. Protan and deutan vector thresholds increased linearly with age while the tritan vector threshold was described with a bilinear model. Analysis and modeling demonstrated that the nominal vectors of the CCT are shifted by senescent changes in ocular media density, and a method for correcting the CCT vectors is demonstrated. A correction for these shifts indicates that classification among individuals of different ages is unaffected. New vector thresholds for elderly observers and for all age groups are suggested based on calculated tolerance limits.

The Change of Expression Configuration Affects Identity-Dependent Expression Aftereffect but Not Identity-Independent Expression Aftereffect.

The present study examined the influence of expression configuration on cross-identity expression aftereffect. The expression configuration refers to the spatial arrangement of facial features in a face for conveying an emotion, e.g., an open-mouth smile vs. a closed-mouth smile. In the first of two experiments, the expression aftereffect is measured using a cross-identity/cross-expression configuration factorial design. The facial identities of test faces were the same or different from the adaptor, while orthogonally, the expression configurations of those facial identities were also the same or different. The results show that the change of expression configuration impaired the expression aftereffect when the facial identities of adaptor and tests were the same; however, the impairment effect disappears when facial identities were different, indicating the identity-independent expression representation is more robust to the change of the expression configuration in comparison with the identity-dependent expression representation. In the second experiment, we used schematic line faces as adaptors and real faces as tests to minimize the similarity between the adaptor and tests, which is expected to exclude the contribution from the identity-dependent expression representation to expression aftereffect. The second experiment yields a similar result as the identity-independent expression aftereffect observed in Experiment 1. The findings indicate the different neural sensitivities to expression configuration for identity-dependent and identity-independent expression systems.

Amplitude difference and similar time course of impulse responses in positive- and negative-contrast detection.

Temporal impulse response functions (IRFs) were measured to investigate the temporal characteristics of positive- and negative-contrast detection in human vision. The IRFs were estimated using models from sequential double-pulse thresholds measured by the psi method. The results indicated that thresholds for positive contrast detection were significantly higher than those for negative contrast detection. However, positive- and negative-contrast IRFs were similar except for the first peak amplitude, reflecting the difference in sensitivity that originates from the summation operation rather than the linear filtering of the visual system.

Aging of human short-wave cone pathways.

The retinal image is sampled concurrently, and largely independently, by three physiologically and anatomically distinct pathways, each with separate ON and OFF subdivisions. The retinal circuitry giving rise to an ON pathway receiving input from the short-wave-sensitive (S) cones is well understood, but the S-cone OFF circuitry is more controversial. Here, we characterize the temporal properties of putative S-cone ON and OFF pathways in younger and older observers by measuring thresholds for stimuli that produce increases or decreases in S-cone stimulation, while the middle- and long-wave-sensitive cones are unmodulated. We characterize the data in terms of an impulse response function, the theoretical response to a flash of infinitely short duration, from which the response to any temporally varying stimulus may be predicted. Results show that the S-cone response to increments is faster than to decrements, but this difference is significantly greater for older individuals. The impulse response function amplitudes for increment and decrement responses are highly correlated across individuals, whereas the timing is not. This strongly suggests that the amplitude is controlled by neural circuitry that is common to S-cone ON and OFF responses (photoreceptors), whereas the timing is controlled by separate postreceptoral pathways. The slower response of the putative OFF pathway is ascribed to different retinal circuitry, possibly attributable to a sign-inverting amacrine cell not present in the ON pathway. It is significant that this pathway is affected selectively in the elderly by becoming slower, whereas the temporal properties of the S-cone ON response are stable across the life span of an individual.

The functional role of alternation advantage in the sequence effect of symbolic cueing with nonpredictive arrow cues.

Previous studies have shown that attention orienting is influenced by the orienting processes of previous trials in a spatial-cueing paradigm. This sequence effect is due to the fact that performance is facilitated when cue validity (valid or invalid) repeats between trials. In this study, we investigated the influences of cue direction and target location on the sequence effect of symbolic cueing with a nonpredictive central arrow cue. The cue direction was manipulated to always point in a certain direction in one condition, and to always point in the opposite direction in a second condition. The results showed that sequence effects were enhanced by the alternation of cue direction and target location and were impaired by the repetition of cue direction and target location. The same result pattern was found when the cue direction was chosen randomly in the third condition. The results suggested that both the repetition advantage effect of cue validity and the alternation advantage effect of cue direction and target location are involved in the sequence effect within the symbolic-cueing paradigm.