Color adaptation in a yellow-blue system: proof of a simple numerical relationship]

Three axes in color space are specified: a (unique) yellow - (unique) blue axis, a (unique) green - magenta axis and brightness. Based on the two chromatic axes two linear opponent colors systems are defined: a red/green-system and a yellowish/bluish-system. A numerical relation is presented to describe color adaptation for the yellowish/bluish-system under adaptation to (unique) yellow and (unique) blue: two pairs of color stimuli are equivalent with regard to the yellowish/bluish-system - consisting of a test stimulus and an adaptation stimulus, respectively - if the ratios from the yellowish/bluish-coordinates of test stimulus and adaptation stimulus are identical. A control of brightness and the red/green-system is presupposed. For several (unique) yellow and (unique) blue adaptation stimuli it is examined how a test stimulus that appears neither yellowish nor bluish changes its location on the (unique) yellow - (unique) blue axis within color space. Three observers take part in the experiment. For each observer a plane of constant brightness and the opponent colors axes are estimated experimentally. The data show that the ratios from the yellowish/bluish coordinates of test stimulus and adaptation stimulus are essentially constant. The results are compared with analogous data for the red/green-system. The findings provide evidence for the specification of the three phenomenal axes. The specification is discussed with regard to Hering's opponent colors theory and Krauskopf's three "cardinal" axes [1982, Vision Research, 22, 1123-1131].     

A ratio principle for a red/green and a yellow/blue channel?

There is strong empirical evidence that, under adaptation to another achromatic color stimulus, the lightness of an achromatic color stimulus depends on the ratio of the luminances of the two stimuli. In the present study, the suitability of this ratio principle is tested for two chromatic postreceptoral opponent channels. A Hering red/green channel and a non-Hering yellow/blue channel are specified as chromatic channels. The yellow/blue channel is defined by extrapolating the plane corresponding to unique green-white linearly to the reddish part of color space, using the plane’s surface as the channel’s equilibria. The experiment was run on an isoluminant plane, measured individually for each observer. Moving along an observer’s measured opponent axes, eight adaptation stimuli were selected for each channel and spanned the whole range of the channel’s coordinates. Red/green equilibria or yellow/blue equilibria were measured as excursions along the adaptation axes. For both presumed channels, the ratios of the equilibrium coordinates of test and adaptation stimuli were essentially constant. This supports the principle’s suitability. However, small asymmetries were found with respect to each channel’s opponent hues. The status of the proposed yellow/blue channel is discussed, as are conditions that might have favored the present findings.     

Effects of spatial filtering and lack of effects of visual imagery on pattern-contingent color aftereffects

Checkerboards contain fundamental two-dimensional Fourier components oriented 45° from the edges of individual checks. Previous studies have shown that contingent color aftereffects following adaptation to chromatic checkerboard stimuli were associated with the fundamental components rather than the edges, In the present experiments, we measured contingent color aftereffects, using the method of constant stimuli, after subjects adapted to unfiltered checkerboards and checkerboards with the fundamental Fourier components removed. The adaptation stimuli were magenta (or green) squares and green (or magenta) diamonds; the test stimuli were vertical or oblique sine-wave gratings with different saturations, After adaptation to unfiltered checkerboards, aftereffects contingent on the fundamental components were obtained. In contrast, after adaptation to filtered stimuli, aftereffects of smaller magnitude were found to be aligned with the edges. The data support the previous findings of spatial-frequency-contingent color after-effects with checkerboard adaptation stimuli and indicate that the aftereffects can be associated with edges if the fundamental components of adaptation stimuli are removed by spatial filtering. We reexamined the possibility of color aftereffects induced by imagery of checkerboards. Contrary to the previous reports, no significant aftereffects were obtained.     

Are there nontrivial constraints on colour categorization?

In this target article the following hypotheses are discussed: (1) Colour is autonomous: a perceptuolinguistic and behavioural universal. (2) It is completely described by three independent attributes: hue, brightness, and saturation: (3) Phenomenologically and psychophysically there are four unique hues: red, green, blue, and yellow; (4) The unique hues are underpinned by two opponent psychophysical and/or neuronal channels: red/green, blue/yellow. The relevant literature is reviewed. We conclude: (i) Psychophysics and neurophysiology fail to set nontrivial constraints on colour categorization. (ii) Linguistic evidence provides no grounds for the universality of basic colour categories. (iii) Neither the opponent hues red/green, blue/yellow nor hue, brightness, and saturation are intrinsic to a universal concept of colour. (iv) Colour is not autonomous.     

The Stiles summation index applied to heterochromatic brightness matching

The summation index technique introduced by Stiles has been applied to heterochromatic brightness matching in order to explain individual differences in luminous efficiency functions for brightness. Such functions were obtained for 2-deg and 10-deg fields from twelve subjects, and the difference between the two fields was compared with the macular pigment density tabulated in Wyszecki and Stiles's book. A summation index was obtained for red and green stimuli combinations and the results are expressed in the form of an equation with nonlinear coefficients. The same equation is applied to the brightness luminous efficiency functions and the individual differences in the efficiency function are interpreted as the result of different contributions of opponent chromatic channels to the perception of brightness.     

The structure of color experience and the existence of surface colors

Color experience is structured. Some “unique” colors (red, green, yellow, and blue) appear as “pure,” or containing no trace of any other color. Others can be considered as a mixture of these colors, or as “binary colors.” According to a widespread assumption, this unique/binary structure of color experience is to be explained in terms of neurophysiological structuring (e.g., by opponent processes) and has no genuine explanatory basis in the physical stimulus. The argument from structure builds on these assumptions to argue that colors are not properties of surfaces and that color experiences are neural processes without environmental counterparts. We reconsider the argument both in terms of its logic and in the light of recent models in vision science which point at environment-involving patterns that may be at the basis of the unique/binary structure of color experience. We conclude that, in the light of internal and external problems which arise for it, the argument from structure fails.     

Nonlinearity in color space measured by apparent motion

We used an apparent motion technique to examine the intensity coding along the three cardinal axes of color space: achromatic (L + M + S), L-M cone, and S cone axes. Two horizontal bars of different colors were alternated to produce a vertical displacement. The color of the background was a mixture varied between the colors of the two bars. When the background color was close to either of the test colors, only the bar that was more salient appeared to jump. Observers adjusted the color of the background until they saw either the two bars moved equally frequently or both bars moved at once. If the color difference in a linear cone excitation space controls this apparent motion, the setting should be midway between the two colors. All of the three cardinal axes showed some deviation from linear behavior. The nonlinearity was less extreme than a logarithmic function for both the achromatic and S cone axes and could be attributed to a small compressive nonlinearity, possibly at the level of cone responses. However, the L-M stimuli showed a more extreme departure from linearity, which suggested a nonlinearity at an opponent site. A test of perceived contrast judgments did not show this nonlinearity for L-M axis, suggesting that it is specific to the L-M contribution to apparent motion.     

Color opponency in synaesthetic experiences

Grapheme-color synaesthesia is a rare condition in which perception of a letter or a digit is associated with concurrent perception of a color. Synaesthetes report that these color experiences are vivid and realistic. We used a Stroop task to show that synaesthetically induced color, like real color, is processed in color-opponent channels (red-green or blue-yellow). Synaesthetic color produced maximal interference with the perception and naming of the real color of a grapheme if the real color was opponent to the synaesthetic color. Interference was reduced considerably if the synaesthetic and real colors engaged different color channels (e.g., synaesthetic blue and real red). No dependence on color opponency was found for semantic conflicts between shape and color (e.g., a blue lemon). Thus, the neural representation of synaesthetic colors closely resembles that of real colors. This suggests involvement of early stages of visual processing in color synaesthesia and explains the vivid and realistic nature of synaesthetic experiences.     

语言和文化影响颜色认知：直接语言效应抑或间接语言效应?

语言和文化对颜色认知的影响存在着直接语言效应和间接语言效应的争论。直接语言效应是指在识记颜色时人先将颜色转换成颜色名称, 再认时通过匹配保留在记忆中的颜色词与目标颜色名称来完成任务。颜色类别知觉是语言策略的结果。间接语言效应是指语言和文化塑造颜色知觉表征, 形成了一个曲形颜色知觉空间, 将人们的注意引向语言和文化定义的颜色类别分界。即使没有语言策略的参与, 类别效应也会出现。颜色文化是民族文化的重要组成部分。绿色和红色在维吾尔族和汉族的语言和文化中分别具有重要的意义。采用颜色相似性判断、颜色分类和颜色再认任务, 考察维吾尔族和汉族的大学生对红、绿的认知, 探查语言和文化对颜色认知的影响及其性质。结果表明, 与汉族相比, 维吾尔族对绿色的辨认、分类和再认存在反应优势, 对红色认知存在反应劣势。与颜色辨认反应比, 两个民族的颜色再认反应时显著长。整个研究表明, 语言和文化对颜色认知的影响存在着间接语言效应, 语言与文化塑造个体的颜色知觉空间。     

Color measurement and color theory: II. Opponent-colors theory

Quantitative opponent-colors theory is based on cancellation of redness by admixture of a standard green, of greenness by admixture of a standard red, of yellowness by blue, and of blueness by yellow. The fundamental data are therefore the equilibrium colors: the set A₁ of lights that are in red/green equilibrium and the set A₂ of lights that are in yellow/blue equilibrium. The result that a cancellation function is linearly related to the color-matching functions can be proved from more basic axioms, particularly, the closure of the set of equilibrium colors under linear operations. Measurement analysis treats this as a representation theorem, in which the closure properties are axioms and in which the colorimetric homomorphism has the cancellation functions as two of its coordinates.Consideration of equivalence relations based on opponent cancellation leads to a further step: analysis of equivalence relations based on direct matching of hue attributes. For additive whiteness matching, this yields a simple extension of the representation theorem, in which the third coordinate is luminance. For other attributes, precise representation theorems must await a better qualitative characterization of various nonlinear phenomena, especially the veiling of one hue attribute by another and the various hue shifts.     

Further studies of the McCollough effect

Following prolonged viewing of black and white striped pattems in colored light, red and green aftereffects that lasted as long as 3 days were seen on the patterns, illuminated with white light. Altemate exposures of a vertical pattern of stripes in green light and a horizontal in white light (or a vertical in white light and a horizontal in red light) produced a red aftereffect on the vertical pattern and a green on the horizontal. The red and green aftereffects were also produced with a single vertical pattern. Adaptation colors that were at all greenish produced a red aftereffect on a vertical pattern and a green on a horizontal, whereas colors that were at all reddish produced a green aftereffect on a vertical pattern and a red on a horizontal. Colors near pure blue and pure yellow, which had little red or green content, produced weak aftereffects. The saturation of the aftereffects on the vertical grating varied in proportion to the red or green content of the adaptation color. Vivid red and green aftereffects were frequently obtained with the vertical and horizontal adaptation patterns paired with colors that closely bracketed pure yellow or pure blue. In all cases, the aftereffects gradually desaturated as the head was gradually tilted down to the side; the colors on each test pattern, vertical and horizontal, vanished at 45-deghead tilt and reversed beyond 45 deg.     

How do we select multiple features? Transient costs for selecting two colors rather than one,persistent costs for color–location conjunctions

In a previous study Lo, Howard, & Holcombe (Vision Research 63:20–33, 2012), selecting two colors did not induce a performance cost, relative to selecting one color. For example, requiring possible report of both a green and a red target did not yield a worse performance than when both targets were green. Yet a cost of selecting multiple colors was observed when selection needed be contingent on both color and location. When selecting a red target to the left and a green target to the right, superimposing a green distractor to the left and a red distractor to the right impeded performance. Possibly, participants cannot confine attention to a color at a particular location. As a result, distractors that share the target colors disrupt attentional selection of the targets. The attempt to select the targets must then be repeated, which increases the likelihood that the trial terminates when selection is not effective, even for long trials. Consistent with this, here we find a persistent cost of selecting two colors when the conjunction of color and location is needed, but the cost is confined to short exposure durations when the observer just has to monitor red and green stimuli without the need to use the location information. These results suggest that selecting two colors is time-consuming but effective, whereas selection of simultaneous conjunctions is never entirely successful.     

Sex-Dimorphic Color Preference in Children with Gender Identity Disorder: A Comparison to Clinical and Community Controls

The present study was designed to assess sex-dimorphic color preferences in children with gender identity disorder (47 boys, 18 girls), clinical controls (65 boys, 35 girls), and community controls (65 boys, 35 girls). The mean age of the children was 7.63 years (range?=?3–12 years). Children were shown a hexagon-shaped display of 144 colors extracted from PowerPoint?. Each child was asked to choose his or her three favorite colors (Trials 1–3) by pointing to them, naming them, and then to provide a justification for each choice. From the entire array, children labeled a total of 11 different colors: black, blue, brown, gray, green, orange, pink, purple, red, white, and yellow. For three of the colors (blue, pink/purple, and red), there was evidence for normative sex differences in color preference, and, for the colors blue and pink/purple, the gender-referred children showed inverted patterns of color preference. For the color blue, luminance values showed that the gender-referred boys and control girls preferred lighter shades, whereas the gender-referred girls and control boys preferred darker shades. Qualitative analysis indicated that gender-specific justifications were uncommon, even for the sex-dimorphic colors. Gender-referred children showed inverted gender-stereotyped color preferences, which are likely related to their more general pattern of cross-gender identification. Principles of gender-differentiated development derived from gender-schema theory are used to explain the group differences in color preferences.     

Limitations on the parallel guidance of visual search: color x color and orientation x orientation conjunctions

In visual search for a conjunction it is much more difficult to search for the conjunction of 2 colors or 2 orientations than for Color x Orientation or Color x Shape conjunctions. The result is not limited to particular colors or shapes. Two colors cannot occupy the same spatial location in Color x Color searches. However, Experiments 6 and 7 show that Color x Shape searches remain efficient even if the color and shape are spatially separated. Our guided search model suggests that in searches for Color x Shape, a parallel color module can guide attention toward the correct color, whereas the shape module guides attention toward the correct shape. Together these 2 sources of guidance lead attention to the target. However, if a target is red and green among red-blue and green-blue distractors, it is not possible to guide search independently toward red items and green items or away from all blue items.     

The Impact of Stimuli Color in Lexical Decision and Semantic Word Categorization Tasks

In two experiments, we examined the impact of color on cognitive performance by asking participants to categorize stimuli presented in three different colors: red, green, and gray (baseline). Participants were either asked to categorize the meaning of words as related to the concepts of “go” or “stop” (Experiment 1) or to indicate if a neutral verbal stimulus was a word or not (lexical decision task, Experiment 2). Overall, we observed performance facilitation in response to go stimuli presented in green (vs. red or gray) and performance inhibition in response to go stimuli presented in red. The opposite pattern was observed for stop‐related stimuli. Importantly, results also indicated that color might also be used to categorize neutral stimuli. Overall, these findings provide support to the green‐go and red‐stop color associations and test the potential functional autonomy acquired by these colors and the boundary conditions to their effects on stimuli categorization.     

Linear and nonlinear opponent color coding

The linearity axiom as proposed by Krantz (1975) is confirmed for red/green equilibria, i.e., lights which appear neither reddish nor greenish (unique yellows, unique blues, and achromatic colors). This experiment also gave some evidence of “veiling,” i.e., the masking of a weak hue component by a strong one. In a second experiment, hue magnitude estimates (HME) for the green component were obtained in variable mixtures of unique green and unique yellow stimuli. Contrary to the suggestion raised by the work of Yager and Taylor (1970), we did not find the relation between the HME and the luminance of the green stimulus to be independent of the amount of added yellow. A relation proposed by Indow and Stevens (1966), in which the proportion of the green luminance is taken as the relevant psychophysical unit, gives a better fit to our data. It is shown, however, that alternative interpretations of such data are possible and that this type of experiment cannot be conclusive regarding the issue of the possibility of absolute judgment of opponent hue attributes.

     

Children's Perception of Munsell Colors

This study examined perception of Munsell notation color by seven third-graders and three college adults (both with normal color vision) and three children (from the same family) who were red-green color blind. The stimuli varied in terms of Munsell Hue (red, green, and purple), Munsell Value (brightness), and Munsell Chroma (saturation). Each S judged the dissimilarity of 325 color pairs (from 26 stimuli). The data were analyzed via individual difference multidimensional scaling that defined a common perceptual space for the group. The results indicated that the third-graders’ color perception was like that of the adults. The color circle was reproduced, as were dimensions based on Munsell Value and Chroma. The color deficient children's data did not fit into that common space. Their perception was guided primarily by the brightness of the stimulus. In sum, the data indicated that, for the domain of Munsell colors, results obtained from adults concerning the dimensionality of the color space could be applied to young children (as long as they have normal color vision).     

Outflow and inflow in movement duplication

Following prolonged exposure to two vertical grating patterns differing in spatial frequency—one pattern illuminated in green light alternated with the other pattern illuminated in red light—human observers will sometimes report seeing desaturated complementary colors when presented with a neutrally illuminated test field consisting of adjacent halves of the two adapting gratings. The number of such color reports increases as the difference between the spatial frequencies of the adapting gratings increases. This frequency-specific chromatic aftereffect is similar to that obtained with orientation-specific color adaptation and may be mediated by neural “channels,” sensitive to both color and frequency input, which are similar to units known to exist in the visual systems of lower organisms.     

When colors backfire: The impact of color cues on moral judgment

This article investigates if and how the valence of color cues affects moral acceptability of (un)desirable consumer behaviors. Study 1 uses colors with definite differences in terms of valence, namely, red and green. Study 2 applies an evaluative conditioning paradigm to endow initially neutral colors with negative versus positive valences. We find an ironic color effect: undesirable behaviors become more acceptable when presented with negatively valenced colors. In general, respondents find (un)desirable behaviors more acceptable when a background color is of the same valence rather than neutral or opposite in valence. Implications for promotion and prevention campaigns are discussed.     

Autoshaped responding: A baseline for studying stimulus preference

In an autoshaping procedure with pigeons, trials consisted of the illumination of two keys, each with a different color, and then a response-independent feeder operation. Over successive conditions, all key-color pairs were arranged from the set of amber, red, green, and blue lamps. During sessions with a given pair, the left-right configuration of the colors varied irregularly, and the two colors alternated in illuminating the feeder. With one red and one green key, for example, red appeared sometimes on the left and sometimes on the right, and the feeder was alternately lit red or green on successive trials. Both total pecks and proportion of trials with at least one peck on a key of a given color were generally greater for red and amber than for green and blue, and relations among preferences were generally transitive across different color pairs. Repeating the procedure with decreased red and amber intensities and increased green and blue intensities reduced red and amber pecking relative to green and blue pecking, implying that differences in responding were determined more strongly by intensive than by chromatic properties of the stimuli.