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Eye design and color signaling in a stomatopod crustacean Gonodactylus smithii.

Many species of stomatopod crustaceans have multiple spectral classes of photoreceptors in their retinas. Behavioral evidence also indicates that stomatopods are capable of discriminating objects by their spectral differences alone. Most animals use only two to four different types of photoreceptors in their color vision systems, typically with broad sensitivity functions, but the stomatopods apparently include eight or more narrowband photoreceptor classes for color recognition. It is also known that stomatopods use several colored body regions in social interactions. To examine why stomatopods may be so 'concerned' with color, we measured the absorption spectra of visual pigments and intrarhabdomal filters, and the reflectance spectra from different parts of the bodies of several individuals of the gonodactyloid stomatopod species, Gonodactylus smithii. We then applied a model of multiple dichromatic channels for color encoding to examine whether the finely tuned color vision was specifically co-evolved with their complex color signals. Although the eye design of stomatopods seems suitable for detecting color signals of their own, the detection of color signals from other animals, such as reef fishes, can be enhanced as well. Color vision in G. smithii is therefore not exclusively adapted to detect its own color signals, but the spectral tuning of some photoreceptors (e.g. midband Rows 2 and 3) enhances the contrast of certain color signals to a large enough degree to make co-evolution between color vision and these rather specific color signals likely.

Animals↗

Color amplitude imaging: preliminary results using vascular sonographic contrast agents.

Conventional (mean Doppler frequency shift) color Doppler imaging and a new method of displaying blood flow in color that uses the amplitude of the Doppler signal were utilized to evaluate three vascular sonographic contrast agents. To compare the two color flow detection modalities, a total of 20 pairs of contrast agent injections were performed while imaging a variety of abdominal organs and tumors in experimental animal models. The 20 paired injections were scored independently to indicate whether color amplitude imaging better demonstrated the effects of contrast enhancement (n = 14), both techniques were equivalent in demonstrating the effects of contrast enhancement (n = 4), or color Doppler imaging better demonstrated the effects of contrast enhancement (n = 2). These results indicate that compared to color Doppler imaging, color amplitude imaging improved visualization of both normal and abnormal blood flow in 70% of these cases (P < 0.0001). Specifically, with contrast enhancement of the Doppler signals, organ vascularity and regional differences in parenchymal blood flow were better demonstrated with color amplitude imaging than with color Doppler imaging. In addition, since color amplitude imaging is nondirectional and less angle dependent than color Doppler imaging, it was possible to visualize vessel continuity more completely and to demonstrate vessel branching more clearly with this modality. However, owing to the lack of directivity and poor temporal resolution, information obtained with color amplitude imaging appears to be complementary to that of color Doppler imaging. In conclusion, color amplitude imaging is a reliable method of determining the effectiveness of vascular sonographic contrast agents and should be considered one of the primary flow imaging modalities used for the assessment of these agents.

Animals↗

Specificity of color connectivity between primate V1 and V2.

To examine the functional interactions between the color and form pathways in the primate visual cortex, we have examined the functional connectivity between pairs of color oriented and nonoriented V1 and V2 neurons in Macaque monkeys. Optical imaging maps for color selectivity, orientation preference, and ocular dominance were used to identify specific functional compartments within V1 and V2 (blobs and thin stripes). These sites then were targeted with multiple electrodes, single neurons isolated, and their receptive fields characterized for orientation selectivity and color selectivity. Functional interactions between pairs of V1 and V2 neurons were inferred by cross-correlation analysis of spike firing. Three types of color interactions were studied: nonoriented V1/nonoriented V2 cell pairs, nonoriented V1/oriented V2 cell pairs, and oriented V1/nonoriented V2 cell pairs. In general, interactions between V1 and V2 neurons are highly dependent on color matching. Different cell pairs exhibited differing dependencies on spatial overlap. Interactions between nonoriented color cells in V1 and V2 are dependent on color matching but not on receptive field overlap, suggesting a role for these interactions in coding of color surfaces. In contrast, interactions between nonoriented V1 and oriented V2 color cells exhibit a strong dependency on receptive field overlap, suggesting a separate pathway for processing of color contour information. Yet another pattern of connectivity was observed between oriented V1 and nonoriented V2 cells; these cells exhibited interactions only when receptive fields were far apart and failed to interact when spatially overlapped. Such interactions may underlie the induction of color and brightness percepts from border contrasts. Our findings thus suggest the presence of separate color pathways between V1 and V2, each with differing patterns of convergence and divergence and distinct roles in color and form vision.

Animals↗

Color, consciousness, and the isomorphism constraint.

The relations among consciousness, brain behavior, and scientific explanation are explored in the domain of color perception. Current scientific knowledge about color similarity, color composition, dimensional structure, unique colors, and color categories is used to assess Locke's "inverted spectrum argument" about the undetectability of color transformations. A symmetry analysis of color space shows that the literal interpretation of this argument--reversing the experience of a rainbow--would not work. Three other color to color transformations might work, however, depending on the relevance of certain color categories. The approach is then generalized to examine behavioral detection of arbitrary differences in color experiences, leading to the formulation of a principled distinction, called the "isomorphism constraint," between what can and cannot be determined about the nature of color experience by objective behavioral means. Finally, the prospects for achieving a biologically based explanation of color experience below the level of isomorphism are considered in light of the limitations of behavioral methods. Within-subject designs using biological interventions hold the greatest promise for scientific progress on consciousness, but objective knowledge of another person's experience appears impossible. The implications of these arguments for functionalism are discussed.

Color↗

Transitions between color categories mapped with a reverse Stroop task.

In the reverse Stroop task, observers are instructed to ignore the ink color in which a color word is printed (the distractor color) and to respond to the meaning of the color word (the target). Reaction times (RTs) are faster with congruent combinations when the ink color matches the word than with incongruent combinations when the ink color does not match the word. We manipulated the distracting ink color from congruent to incongruent and measured the transition from facilitation to interference. In Experiment 1, we confirmed that this transition could be assessed independently from the contextual influence of particular sets of stimuli and responses, implying that the color space in which interference and facilitation occurs is generalizable. In Experiment 2, we obtained reverse Stroop data for transitions between red and yellow, yellow and green, green and blue, and blue and red, and compared them with independent estimates of color appearance obtained by hue scaling for the same chromaticity samples. We find that the magnitude of the reverse Stroop effect can provide a reliable index of the similarity of color appearance between the distracting chromaticity and the color category represented by the target color word. Moreover, it will allow us to quantify the mapping between the chromaticity space defined at the cone photoreceptors and a cognitive color space defined at an advanced level of neural processing.

Color↗

Interaction of color and geometric cues in depth perception: when does "red" mean "near"?

Luminance and color are strong and self-sufficient cues to pictorial depth in visual scenes and images. The present study investigates the conditions under which luminance or color either strengthens or overrides geometric depth cues. We investigated how luminance contrast associated with the color red and color contrast interact with relative height in the visual field, partial occlusion, and interposition to determine the probability that a given figure presented in a pair is perceived as "nearer" than the other. Latencies of "near" responses were analyzed to test for effects of attentional selection. Figures in a pair were supported by luminance contrast (Experiment 1) or isoluminant color contrast (Experiment 2) and combined with one of the three geometric cues. The results of Experiment 1 show that the luminance contrast of a color (here red), when it does not interact with other colors, produces the same effects as achromatic luminance contrasts. The probability of "near" increases with the luminance contrast of the color stimulus, the latencies for "near" responses decrease with increasing luminance contrast. Partial occlusion is found to be a strong enough pictorial cue to support a weaker red luminance contrast. Interposition cues lose out against cues of spatial position and partial occlusion. The results of Experiment 2, with isoluminant displays of varying color contrast, reveal that red color contrast on a light background supported by any of the three geometric cues wins over green or white supported by any of the three geometric cues. On a dark background, red color contrast supported by the interposition cue loses out against green or white color contrast supported by partial occlusion. These findings reveal that color is not an independent depth cue, but is strongly influenced by luminance contrast and stimulus geometry. Systematically shorter response latencies for stronger "near" percepts demonstrate that selective visual attention reliably detects the most likely depth cue combination in a given configuration.

Color Perception↗

Contrast effects of the three primary colors on human visual evoked potentials.

In this study we evaluated in humans the question of whether contrast effects with patterned color stimuli varied in the same way as is known to occur with black-and-white stimuli. Using a counterphasing checkerboard pattern, we evaluated the steady-state visual evoked potential (VEP) in 10 subjects for the response to different contrast levels in each of the 3 primary colors. Overall mean luminance of each color was photometrically equated and kept constant during all trials. The VEP was computer-averaged for 90 consecutive 1 sec epochs of stimulation, and the power at the appropriate frequency was calculated. For each color, the contrast-response curves revealed small power values at low contrast (0.1) and larger power at the 3 high-contrast settings (0.3-0.5). Power varied markedly by color and by subject. The shape of the curves, depending on color and subject, often indicated a saturation of response. A given subject commonly had a physiologically 'preferred' color in that the power with that color was consistently larger. Most subjects had definite subjective color 'preferences,' believing that they perceived the contrast better for one or two colors. However, these impressions were often not validated by the VEP responses to the various colors. These results indicate that white-light VEP responses may not necessarily reflect the response characteristics of specific colors, nor do they necessarily reflect the large inter- and intra-subject differences in color responses noted in this study.

Adult↗

Adaptive modulation of color salience contingent upon global form coding and task relevance.

Extensive research on local color aftereffects has revealed perceptual consequences of opponent color coding in the retina and the LGN, and of orientation-and/or spatial-frequency-contingent color coding in early cortical visual areas (e.g., V1 and V2). Here, we report a color aftereffect that depends crucially on global-form-contingent color processing. Brief viewing of colored items (passively viewed, ignored, or attended) reduced the salience of the previewed color in a subsequent task of color-based visual search. This color-salience aftereffect was relatively insensitive to variations (between color preview and search) in local image features, but was substantially affected by changes in global configuration (e.g. the presence or absence of perceptual unitization); the global-form dependence of the aftereffect was also modulated by task demands. The overall results suggest that (1) color salience is adaptively modulated (from fixation to fixation), drawing attention to a new color in visual-search contexts, and (2) these modulations seem to be mediated by global-form-and-color-selective neural processing in mid to late stages of the ventral visual pathway (e.g., V4 and IT), in combination with task-dependent feedback from higher cortical areas (e.g., prefrontal cortex).

Attention↗

The role of iron and the factors affecting off-color development of polyphenols.

Iron deficiency affects over two billion people worldwide (Lotfi, M.; Venkatesh Mannar, M. G.; Merx, R. J.; Naber-van den Heuvel, P. Micronutrient Fortification of Foods: Current Practices, Research,and Opportunities; Micronutrient Initiative: Ottawa, Ontario, Canada, 1996). However, fortifying foods with highly bioavailable iron is technically challenging because of off-color and off-flavor development, catalytic degradation of vitamins, and oxidation of lipids. The role of highly bioavailable iron in the off-color development of foods and beverages is not well-understood. The goal of this research was to examine the interaction of iron with simple phenolics and polyphenols. Factors that may affect off-color development, such as pH, oxygen, temperature, and reducing and chelating agents, were evaluated as a model for food products. Our results demonstrated that the iron that reacts with the simple phenolic, catechol, to develop off-color must be in the oxidized state, and the iron is reduced in the presence of catechol. Because this is an oxidation/reduction reaction, the redox potential of all of the components is critical to the color development. Ferrous iron sources with low redox potentials and ferric iron sources with high redox potentials caused off-color development with catechol. Only polyphenols that contain ortho-hydroxyl groups cause off-color development with iron. All of the factors tested affect off-color development and redox potential of the system. Low pH, low oxygen, high temperature, and the presence of reducing and chelating agents inhibited off-color development. To confirm the model, foods that contained these polyphenols were evaluated for off-color development when iron was added. The foods tested reacted similarly to the models of polyphenols with iron. Off-color development was caused by oxidation-reduction interactions between ferric iron and polyphenols that contained ortho-dihydroxyl groups. Ferrous iron needed to be oxidized to participate in off-color development. In addition, methods identified in the models to prevent off-color development were effective in most of the food products examined. Using the ferrous form of iron and maintaining it in its reduced form by lowering pH, removing oxygen, and including reducing agents, it was possible to fortify foods with highly bioavailable iron.

Catechols↗

The spatial transformation of color in the primary visual cortex of the macaque monkey.

Perceptually, color is used to discriminate objects by hue and to identify color boundaries. The primate retina and the lateral geniculate nucleus (LGN) have cell populations sensitive to color modulation, but the role of the primary visual cortex (V1) in color signal processing is uncertain. We re-evaluated color processing in V1 by studying single-neuron responses to luminance and to equiluminant color patterns equated for cone contrast. Many neurons respond robustly to both equiluminant color and luminance modulation (color-luminance cells). Also, there are neurons that prefer luminance (luminance cells), and a few neurons that prefer color (color cells). Surprisingly, most color-luminance cells are spatial-frequency tuned, with approximately equal selectivity for chromatic and achromatic patterns. Therefore, V1 retains the color sensitivity provided by the LGN, and adds spatial selectivity for color boundaries.

Action Potentials↗

Test of a convergence model for color transparency perception.

Models of color transparency suggest that a region in which colors of surfaces converge in color space will appear transparent. The convergence is described by a transparency parameter alpha and a target of convergence. To test such models psychophysically, observers were presented a display with four colored areas. The colors of three of the areas were chosen in advance by the experimenter. The task of the observer was to choose the color of the fourth area to make a central region appear transparent. Settings for the fourth color were collected for a total of twenty-four color combinations chosen from three planes in color space. Observers' settings agreed well with the model, which predicts that choices for the fourth color lie along a line segment in color space that is parameterized by alpha. The results suggest further that color discriminability and color opponency also influence transparency judgment.

Color Perception↗

Primary-consistent soft-decision color demosaicking for digital cameras (patent pending).

Color mosaic sampling schemes are widely used in digital cameras. Given the resolution of CCD sensor arrays, the image quality of digital cameras using mosaic sampling largely depends on the performance of the color demosaicking process. A common problem with existing color demosaicking algorithms is an inconsistency of sample interpolations in different primary color channels, which is the cause of the most objectionable color artifacts. To cure the problem, we propose a new primary-consistent soft-decision framework (PCSD) of color demosaicking. In the PCSD framework, we make multiple estimates of a missing color sample under different hypotheses on edge or texture directions. The estimates are made via a primary consistent interpolation, meaning that all three primary components of a color are interpolated in the same direction. The final estimate of a color sample is obtained by testing different interpolation hypotheses in the reconstructed full-resolution color image and selecting the best via an optimal statistical decision or inference process. A concrete color demosaicking method of the PCSD framework is presented. This new method eliminates certain types of color artifacts of existing color demosaicking methods. Extensive experimental results demonstrate that the PCSD approach can significantly improve the image quality of digital cameras in both subjective and objective measures. In some instances, our gain over the competing methods can be as much as 7 dB.

Algorithms↗

Color processing in macaque striate cortex: electrophysiological properties.

We have shown in the accompanying paper that optical imaging of macaque striate cortex reveals patches that are preferentially activated by equiluminant chromatic gratings compared with luminance gratings. These imaged color patches are highly correlated, although not always in one-to-one correspondence, with the cytochrome-oxidase (CO) blobs. In the present study, we have investigated the electrophysiological properties of neurons in the imaged color patches and the CO blobs. Our results indicate that individual blobs tend to contain cells of only one type of color opponency: either red/green or blue/yellow. Individual imaged color patches, however, can bridge blobs of similar opponency or differing opponency. When imaged color patches contain two blobs of differing opponency, the cells in the bridge region exhibit mixed color properties that are not opponent along the two cardinal color axes (either red/green or blue/yellow). Two blobs within a single imaged color patch receive input from the same eye or from different eyes. In the latter case, the bridge region between blobs contains binocular cells that are color selective. Because the cells recorded in imaged color patches were more color selective and unoriented than cells outside of color patches, color properties appear to be organized in a clustered and segregated fashion in primate V1.

Animals↗

Color processing in macaque striate cortex: relationships to ocular dominance, cytochrome oxidase, and orientation.

We located clusters of color-selective neurons in macaque striate cortex, as mapped with optical imaging and confirmed with electrophysiological recordings. By comparing responses to an equiluminant red/green stimulus versus a high-contrast luminance stimulus, we were able to reveal a patchy distribution of color selectivity. Other color imaging protocols, when compared with electrophysiological data, did not reliably indicate the location of functional structures. The imaged color patches were compared with other known functional subdivisions of striate cortex. There was a high degree of overlap of the color patches with the cytochrome-oxidase (CO) blobs. The patches were often larger than a single blob in size, however, and in some instances spanned two neighboring blobs. More than one-half (56%) of the color-selective patches seen in optical imaging were not confined to one ocular dominance (OD) column. Almost one-quarter of color patches (23%) extended across OD columns to encompass two blobs of different eye preference. We also compared optical images of orientation selectivity to maps of color selectivity. Results indicate that the layout of orientation and color selectivity are not directly related. Specifically, despite having similar scales and distributions, the maps of orientation and color selectivity were not in consistent alignment or registration. Further, we find that the maps of color selectivity and of orientation are each only loosely related to maps of OD. This description stands in contrast to a common depiction of color-selective regions as identical to CO blobs, appearing as pegs in the centers of OD columns in the classical "ice cube" model. These results concerning the pattern of color selectivity in V1 support the view (put forth in previous imaging studies of the organization of orientation and ocular dominance) that there is not a fundamental registration of functional hypercolumns in V1.

Animals↗

Dissociation of color and figure-ground effects in the watercolor illusion.

Two phenomena can be observed in the watercolor illusion: illusory color spreading and figure-ground organization. We performed experiments to determine whether the figure-ground effect is a consequence of the color illusion or due to an independent mechanism. Subjects were tested with displays consisting of six adjacent compartments--three that generated the illusion alternating with three that served for comparison. In a first set of experiments, the illusory color was measured by finding the matching physical color in the alternate compartments. Figureness (probability of 'figure' responses, 2AFC) of the watercolor compartments was then determined with and without the matching color in the alternate compartments. The color match reduced figureness, but did not abolish it. There was a range of colors in which the watercolor compartments dominated as figures over the alternate compartments although the latter appeared more saturated in color. In another experiment, the effect of tinting alternate compartments was measured in displays without watercolor illusion. Figureness increased with color contrast, but its value at the equivalent contrast fell short of the figureness value obtained for the watercolor pattern. Thus, in both experiments, figureness produced by the watercolor pattern was stronger than expected from the color effect, suggesting independent mechanisms. Considering the neurophysiology, we propose that the color illusion follows from the principles of representation of surface color in the visual cortex, while the figure-ground effect results from two mechanisms of border ownership assignment, one that is sensitive to asymmetric shape of edge profile, the other to consistency of color borders.

Adaptation, Ocular↗

Hypnotic visual illusion alters color processing in the brain.

OBJECTIVE: This study was designed to determine whether hypnosis can modulate color perception. Such evidence would provide insight into the nature of hypnosis and its underlying mechanisms. METHOD: Eight highly hypnotizable subjects were asked to see a color pattern in color, a similar gray-scale pattern in color, the color pattern as gray scale, and the gray-scale pattern as gray scale during positron emission tomography scanning by means of [(15)O]CO(2). The classic color area in the fusiform or lingual region of the brain was first identified by analyzing the results when subjects were asked to perceive color as color versus when they were asked to perceive gray scale as gray scale. RESULTS: When subjects were hypnotized, color areas of the left and right hemispheres were activated when they were asked to perceive color, whether they were actually shown the color or the gray-scale stimulus. These brain regions had decreased activation when subjects were told to see gray scale, whether they were actually shown the color or gray-scale stimuli. These results were obtained only during hypnosis in the left hemisphere, whereas blood flow changes reflected instructions to perceive color versus gray scale in the right hemisphere, whether or not subjects had been hypnotized. CONCLUSIONS: Among highly hypnotizable subjects, observed changes in subjective experience achieved during hypnosis were reflected by changes in brain function similar to those that occur in perception. These findings support the claim that hypnosis is a psychological state with distinct neural correlates and is not just the result of adopting a role.

Adult↗

[Study on color of thermosetting resin for veneer crown].

Based on the viewpoint that stresses the importance of achieving natural colors and forms for veneer crown, four representative kinds of thermosetting resins were investigated colorimetrically in an attempt to clarify the relationship between the thickness and color of resins in opaque, dentin and enamel colors respectively. A spectrophotometer was used to measure the colors, the CIE colorimetric system employed to show the readings, and the CIE 1964 U*V*W* space was utilized to indicate the color differences, with the following results. 1. In the case of dentin, certain specific colors were observed for thickness of 1.3 to 1.8 mm when used alone, but when applied over opaque the range was 0.2 to 0.5 mm lower than when used alone. 2. Enamel resins were grouped into two types according to different color groups, one group similar to achromatic color with low limpidity and the other similar to the dentin color with high limpidity. The former type became more grayer with an increase in thickness when applied over dentin. The latter type showed no difference in color even when the thickness increased. This study has shown that the facing color results vary depending on the color properties of the different resins used. Therefore, it is advisable that careful consideration be given to these differencies in order to achieve the intended color facing.

Color↗

Evaluation of soft-tissue masses using segmented color Doppler velocity images: preliminary observations.

OBJECTIVE: We report our initial experience with segmented color Doppler velocity-based estimates of tumor vascularity for various histogically proven soft-tissue masses. SUBJECTS AND METHODS: Color Doppler sonography of 23 histologically proven masses in 22 patients was performed. Digital color Doppler images were acquired directly off the scanner output or from video recordings and stored on a personal computer as 24-bit gray-scale and color composite images. A color Doppler velocity segmentation and analysis algorithm was applied to the digital images, from which we calculated the normalized percentage of color Doppler area. Normalization was determined by expressing color Doppler area as a percentage of the area enclosed by a preselected region of interest. We also calculated mean percentage, SD, and cumulative distribution of color Doppler area, relative to a fixed threshold, for the acquired image data sets. RESULTS: Estimates of mean percentage of color Doppler area showed a dynamic range of at least two or three orders of magnitude between lowest and highest values obtained. A scatterplot of mean percentage of color Doppler area versus SD of percentage of color Doppler area showed a linear monotonic relationship (r2 = .92), illustrating increasing vascular heterogeneity with mean vascularity. Preliminary data also suggest the presence of at least two distinct groups of masses (p < .0001) based on these vascularity estimates. One group corresponds to high-grade lesions in which tumor angiogenesis is expected to be important in predicting biologic behavior. The second group appeared to have little or no relationship to tumor vascularity or was of an intermediate (or lower) histologic grade. CONCLUSION: Quantitative color Doppler estimates of tumor vascularity can be obtained over a wide dynamic range. Such estimates provide a mechanism to assess vascular heterogeneity of soft-tissue tumors. Preliminary data suggest that two biologically distinct groups of masses may be separable on the basis of quantitative velocity-based estimates of tumor vascularity as obtained from color Doppler sonography.

Adolescent↗