Neural basis for unique hues

All colors can be described in terms of four non-reducible ‘unique’ hues: red, green, yellow, and blue [1]. These four hues are also the most common ‘focal’ colors — the best examples of color terms in language [2]. The significance of the unique hues has been recognized since at least the 14^th century [3] and is universal [4] and [5], although there is some individual variation [6] and [7]. Psychophysical linking hypotheses predict an explicit neural representation of unique hues at some stage of the visual system, but no such representation has been described [8]. The special status of the unique hues “remains one of the central mysteries of color science” [9]. Here we report that a population of recently identified cells in posterior inferior temporal cortex of macaque monkey contains an explicit representation of unique hues.     

Contributions of pterin and carotenoid pigments to dewlap coloration in two anole species

Animals can acquire bright coloration using a variety of pigmentary and microstructural mechanisms. Reptiles and amphibians are known to use two types of pigments - pterins and carotenoids - to generate their spectrum of colorful red, orange, and yellow hues. Because both pigment classes can confer all of these hues, the relative importance of pterins versus carotenoids in creating these different colors is not always apparent. We studied the carotenoid and pterin content of red and yellow dewlap regions in two neotropical anole species - the brown anole (Norops sagrei) and the ground anole (N. humilis). Pterins (likely drosopterins) and carotenoids (likely xanthophylls) were present in all tissues from all individuals. Pterins were more enriched in the lateral (red) region, and carotenoids more enriched in the midline (yellow) region in N. humilis, but pterins and carotenoids were found in similar concentrations among lateral and midline regions in N. sagrei. These patterns indicate that both carotenoid and pterin pigments are responsible for producing color in the dichromatic dewlaps of these two species, and that in these two species the two pigments interact differently to produce the observed colors.     

Cone Photoreceptor Sensitivities and Unique Hue Chromatic Responses: Correlation and Causation Imply the Physiological Basis of Unique Hues

This paper relates major functions at the start and end of the color vision process. The process starts with three cone photoreceptors transducing light into electrical responses. Cone sensitivities were once expected to be Red Green Blue color matching functions (to mix colors) but microspectrometry proved otherwise: they instead peak in yellowish, greenish, and blueish hues. These physiological functions are an enigma, unmatched with any set of psychophysical (behavioral) functions. The end-result of the visual process is color sensation, whose essential percepts are unique (or pure) hues red, yellow, green, blue. Unique hues cannot be described by other hues, but can describe all other hues, e.g., that hue is reddish-blue. They are carried by four opponent chromatic response curves but the literature does not specify whether each curve represents a range of hues or only one hue (a unique) over its wavelength range. Here the latter is demonstrated, confirming that opponent chromatic responses define, and may be termed, unique hue chromatic responses. These psychophysical functions also are an enigma, unmatched with any physiological functions or basis. Here both enigmas are solved by demonstrating the three cone sensitivity curves and the three spectral chromatic response curves are almost identical sets (Pearson correlation coefficients r from 0.95–1.0) in peak wavelengths, curve shapes, math functions, and curve crossover wavelengths, though previously unrecognized due to presentation of curves in different formats, e.g., log, linear. (Red chromatic response curve is largely nonspectral and thus derives from two cones.) Close correlation combined with deterministic causation implies cones are the physiological basis of unique hues. This match of three physiological and three psychophysical functions is unique in color vision.     

Reaction times identify a Pavlovian component in a two-choice discrimination

Six pigeons discriminated on discrete trials between two colors. In Experiment 1, two luminous spots were both either blue or green and the reinforced responses were “peck left” for blue and “peck right” for green. In Experiment 2, the hue of a center spot controlled subsequent choice pecks to left or right. In both experiments response bias was manipulated in two ways. During stimulus frequency (“SF”) sessions correct responses brought food on 40% of trials; in “imbalanced” blocks of sessions one hue appeared on 80% of trials and the other on 20%. During reinforcement probability (“RNF”) sessions the hues appeared equally often, but in imbalanced blocks the hues signaled different reinforcement probabilities, either 64% or 16%. In “balanced” control blocks the hues appeared equally often and were both reinforced at 40%. The experiments gave similar results. When bias was computed from choice percentages the imbalanced conditions yielded substantial response bias, and the amount of bias was about the same under RNF and SF treatments. However, reaction times (RTs) gave a different outcome. RNF imbalance slowed responses directed at the less reinforced stimulus, but SF imbalance had little RT effect (Experiment 1) or no effect (Experiment 2). These results suggest that choice was controlled by an instrumental stimulus-response-reinforcement association, whereas RTs were controlled by a Pavlovian stimulus-reinforcement association.     

Dichromatic color language: "reds" and "greens" don't look alike but their colors do.

When protanopes or deuteranopes arrange the Farnsworth Dichotomous Test colors in order of similarity, they reveal their lack of red/green hue discriminations by alternating chips that the normal trichromat sees as reddish and greenish test colors. The dichromatic orderings follow a systematic variation in saturation of blue hues through neutral and into yellow hues as described by theory for each of the two types. Some dichromats who show the typical test behavior nevertheless use reddish and greenish hue terms appropriately when instructed to name the same test colors. Lightness cues are probably used by these dichromats in the naming task but ignored in the perceptual similarity task. Thus, unlike normal trichromats, who use similar names for perceptually similar colors, dichromats may use dissimilar names for perceptually similar colors. In this way they can achieve concordance with the normative language system despite its discordance with their impoverished color perceptions.     

Orthogonal Relations and Color Constancy in Dichromatic Colorblindness

This paper employs uniform color space to analyze relations in dichromacy (protanopia, deuteranopia, tritanopia). Fifty percent or less of dichromats represent the classical reduction form of trichromacy, where one of three cones is inoperative but normal trichromatic color mixture such as complementary colors (pairs that mix white) are accepted by the dichromat, whose data can thus be plotted to CIE chromaticity spaces. The remaining dichromats comprise many and varied more-complex gene arrays from mutations, recombinations, etc. Though perhaps a minority, the three reductionist types provide a simple standard, in genotype and phenotype, to which the more complex remainder may be compared. Here, previously published data on dichromacy are plotted and analyzed in CIELUV uniform color space to find spatial relations in terms of color appearance space (e.g., hue angle). Traditional residual (seen) hues for protanopia and deuteranopia (both red–green colorblindness) are yellow and blue, but analysis indicates the protanopic residual hues are more greenish yellow and reddish blue than in tradition. Results for three illuminants (D65, D50, B) imply four principles in the spatial structure of dichromacy: (1) complementarity of confusion hue pairs and of residual hue pairs; (2) orthogonality of confusion locus and residual hues locus at their intersection with the white point, in each dichromatic type; (3) orthogonality of protanopic and tritanopic confusion loci; and (4) inverse relations between protanopic and tritanopic systems generally, such that one''s confusion hues are the other''s residual hues. Two of the three dichromatic systems do not represent components of normal trichromatic vision as sometimes thought but are quite different. Wavelength shifts between illuminants demonstrate chromatic adaptation correlates exactly with that in trichromatic vision. In theory these results clarify relations in and between types of dichromacy. They also apply in Munsell and CIELAB color spaces but inexactly to the degree they employ inexact complementarity.     

卷蛾分索赤眼蜂雌蜂的颜色偏好性

为了确定卷蛾分索赤眼蜂Trichogrammatoidea bactrae Nagaraja 雌蜂的颜色偏好性, 在室内通过在培养皿底部黏贴彩纸的方法测定卷蛾分索赤眼蜂雌蜂对红、 黄、 黑、 紫、 绿、 白、 蓝7种颜色的行为趋性反应。结果表明, 卷蛾分索赤眼蜂雌蜂在红、 黄、 紫、 绿和蓝5种颜色上的滞留时间都极显著地高于对照（P<0.01）, 在黑和白2种颜色上的滞留时间与对照没有显著差异（P>0.05）; 对黄色的首次选择率极显著高于对照(P< 0.01), 对红、 紫、 绿和蓝色的首次选择率均显著高于对照(P＜0.05), 对黑色和白色的首次选择率与对照没有显著差异。当雌蜂分别在黄与红、 紫、 绿和蓝两两颜色之间选择时, 雌蜂在黄色彩纸上的滞留时间显著长于其他4种颜色。当雌蜂对红、 紫、 绿、 蓝和黄色5种颜色一起选择时, 在首次选择率、 滞留次数上5种颜色间都没有明显差异(P＞0.05); 但在红色和蓝色上的滞留时间显著长于紫色(P＜0.05), 在这3种颜色上的滞留时间与在黄色和绿色上的滞留时间均无显著差异(P＞0.05)。卷蛾分索赤眼蜂雌蜂在7种颜色卵卡上分别与透明纸（对照）上的米蛾卵的选择寄生时, 在黄色卵卡上的寄生卵量极显著多于对照(P＜0.01), 黑色卵卡上的寄生卵量极显著少于对照(P＜0.01), 其他5种颜色的卵卡上的寄生卵量与对照没有显著差异(P＞0.05)。结果说明, 卷蛾分索赤眼蜂雌蜂对黄色最为偏好, 其次偏好红、 紫、 绿和蓝色, 较不喜好白色和黑色。     

Responses of the blister beetle Hycleus apicicornis to visual stimuli

Insect attraction to host plants may be partly mediated by visual stimuli. In the present study, the responses of adult Hycleus apicicornis (Guér.) (Coleoptera: Meloidae) to plant models of different colours, different combinations of two colours, or three hues of blue of different shapes are compared. Single‐colour models comprised the colours sky blue, bright green, yellow, red, white and black. Sky blue (reflecting light in the 440–500 nm region) is the most attractive, followed by white, which reflects light over a broader range (400–700 nm). On landing on sky blue targets, beetles exhibit feeding behaviour immediately. When different hues of blue (of different shapes) are compared, sky blue is preferred over turquoise, followed by dark blue, indicating that H. apicicornis is more attracted to lighter hues of blue than to darker ones. No significant differences are found between the three shapes (circle, square and triangle) tested, suggesting that reflectance associated with colour could be a more important visual cue than shape for host location by H. apicicornis. The preference of H. apicicornis for sky blue can be exploited in designing an attractive trap for its management.     

No compelling positive association between ovarian hormones and wearing red clothing when using multinomial analyses

Several studies report that wearing red clothing enhances women's attractiveness and signals sexual proceptivity to men. The associated hypothesis that women will choose to wear red clothing when fertility is highest, however, has received mixed support from empirical studies. One possible cause of these mixed findings may be methodological. The current study aimed to replicate recent findings suggesting a positive association between hormonal profiles associated with high fertility (high estradiol to progesterone ratios) and the likelihood of wearing red. We compared the effect of the estradiol to progesterone ratio on the probability of wearing: red versus non-red (binary logistic regression); red versus neutral, black, blue, green, orange, multi-color, and gray (multinomial logistic regression); and each of these same colors in separate binary models (e.g., green versus non-green). Red versus non-red analyses showed a positive trend between a high estradiol to progesterone ratio and wearing red, but the effect only arose for younger women and was not robust across samples. We found no compelling evidence for ovarian hormones increasing the probability of wearing red in the other analyses. However, we did find that the probability of wearing neutral was positively associated with the estradiol to progesterone ratio, though the effect did not reach conventional levels of statistical significance. Findings suggest that although ovarian hormones may affect younger women's preference for red clothing under some conditions, the effect is not robust when differentiating amongst other colors of clothing. In addition, the effect of ovarian hormones on clothing color preference may not be specific to the color red.     

CONVERGENT EVOLUTION OF RED CAROTENOID COLORATION IN WIDOWBIRDS AND BISHOPS (EUPLECTES SPP.)

Avian carotenoid‐based signals are classic examples of sexually selected, condition‐dependent threat displays or mate choice cues. In many species, male dominance or mating success is associated with redder (i.e., longer wavelength) color hues, suggesting that red colors are either more efficient or more reliable signals than yellow colors. Few studies, however, have investigated selection for redness in a macroevolutionary context. Here, we phylogenetically reconstruct the evolution of carotenoid coloration in the African widowbirds and bishops (Euplectes spp.), for which agonistic selection for redder hues, as well as pigmentary mechanisms, is well documented. Using reflectance spectrometry for objective color quantification, and accounting for phylogenetic uncertainty, we find that yellow plumage color is a retained ancestral state in Euplectes, and that red color hues have convergently evolved two or three times. Results are discussed in relation to a known diversity in pigment mechanisms, supporting independent origins of red color, and suggesting that agonistic selection and physiological constraints have interacted to generate color diversity in Euplectes.     

Genetic engineering of flavonoid pigments to modify flower color in floricultural plants

Recent advances in genetic transformation techniques enable the production of desirable and novel flower colors in some important floricultural plants. Genetic engineering of novel flower colors is now a practical technology as typified by commercialization of a transgenic blue rose and blue carnation. Many researchers exploit knowledge of flavonoid biosynthesis effectively to obtain unique flower colors. So far, the main pigments targeted for flower color modification are anthocyanins that contribute to a variety of colors such as red, pink and blue, but recent studies have also utilized colorless or faint-colored compounds. For example, chalcones and aurones have been successfully engineered to produce yellow flowers, and flavones and flavonols used to change flower color hues. In this review, we summarize examples of successful flower color modification in floricultural plants focusing on recent advances in techniques.     

Visual stimuli that elicit visual tracking, approaching and striking behavior from an unusual praying mantis, Euchomenella macrops (Insecta: Mantodea)

In comparison to other similarly sized mantis species examined in previous studies, Euchomenella macrops has a significantly smaller head, shorter foreleg tibia, but longer prothorax which have been interpreted as specializations for the capture of smaller, slower prey. We tested this conjecture by assessing the rates at which computer generated stimuli elicit visual tracking, approaching, and striking behaviors by adult females. When presented with black disks moving erratically against a white background, strike rate rose progressively as disks enlarged up to 44 deg (visual angle) if the disks moved rapidly (e.g., 143 deg/s); at slower speeds (113, 127 deg/s), smaller disks (<27 deg) were preferred. When black moved linearly from the visual periphery to visual field center (at 73 or 143 deg/s) and then stopped, E. macrops struck consistently at disks as small as 5 deg after movement ceased. E. macrops also struck at higher rates in response to 23 deg erratically moving (subjective) red (versus subjective blue or green) disks that were luminance matched to a grey background although they tracked all colors at equally high rates. Unlike some other species, E. macrops did not strike at higher rates in response to elongated rectangular stimuli moving parallel (versus perpendicular) to their long axis, although the former elicited higher rates of approaching. An analysis of tracking behavior revealed that virtually all tracking movements were a result of head (versus) prothorax rotation.     

Use of CC traps with different trap base colors for silverleaf whiteflies (Homoptera: Aleyrodidae), thrips (Thysanoptera: Thripidae), and leafhoppers (Homoptera: Cicadellidae)

During 1996, 1997, and 1999, studies were conducted in cotton, sugar beets, alfalfa, yardlong bean, and peanut fields to compare insect catches in CC traps equipped with different trap base colors. The studies were conducted in southwestern United States, China, and India. The nine colors, white, rum, red, yellow, lime green, spring green, woodland green (dark green), true blue, and black, varied in spectral reflectance in the visible (400-700 nm) and near-infrared (700-1050 nm) portions of spectrum. Lime green, yellow, and spring green were the three most attractive trap base colors for silverleaf whitefly, Bemisia argentifolii Bellows & Perring, and leafhopper, Empoasca spp. adults. The three trap base colors were moderately high in the green, yellow, and orange spectral regions (490-600 nm), resembling the spectral reflectance curve of the abaxial (underleaf) surfaces of green cotton leaves. True blue and white were the most attractive trap base colors for western flower thrips, Frankliniella occidentalis (Pergande), adults. The true blue and white trap bases were moderately high in the blue spectral region (400-480 nm).     

Color discrimination in wild boars

Two experiments were carried out in order to clarify the color perception of Japanese wild boarsSus scrofa leucomystax. Two females were trained using an operant conditioning technique to press a switch under a positive stimulus color card in order to receive food as a reward. In Exp. 1, they were tested for discrimination between 3 colors (red, green and blue) and gray. The luminosity of all colors was the same. The wild boars succeeded in discrimination tests between blue and gray, but failed to discriminate red from gray. They also did not discriminate green from gray so clearly as blue from gray. In Exp. 2, the same wild boars were tested to discriminate between 8 kinds of color, which were created by gradating green yellow into red purple except for the 3 colors used in Exp. 1, and gray. They could clearly discriminate blue, purple blue and a part of purple from gray. In these experiments, wild boars were capable of recognizing bluish colors. However, for colors approaching green or yellow, they failed the test by degrees.     

Trying to See Red Through Stickleback Photoreceptors: Functional Substitution of Receptor Sensitivities

A key to understanding animal behavior is knowledge of the sensory information animals extract from their environment. For visually motivated tasks, the information animals obtain through their eyes is often assumed to be essentially the same as that perceived by humans. However, known differences in structure and processing among the visual systems of different animals clearly indicate that the world seen by each is different. A well‐characterized difference between human and other animal visual systems is the number of types and spectral sensitivities of their photoreceptors. We are developing a technique, functional substitution, that exploits knowledge of these differences to portray for human subjects, colors as they would appear through the photoreceptors of another animal. In a specific application, we ask human subjects to rank hues of male threespine stickleback (Gasterosteus aculeatus) throats viewed through stickleback photopigments. We compare these ranks to ranks of the same throat hues viewed through normal human photoreceptors. We find essentially no difference between the two sets of rankings. This suggests that any differences in human and stickleback rankings of such hues would result from differences in post‐receptoral neural processing. Using a previously developed model of stickleback neural processing, we established another ranking of the hues which was again essentially the same as the rankings produced by the human subjects. A growing literature indicates that stickleback do rank such hues in the evaluation of males as potential mates or threats. Although our results do not demonstrate that humans and stickleback use the same mechanisms to assess color, our experiments significantly failed to show that stickleback and human rankings of throat hues should be different. Nevertheless, a comparison of all these rankings to ranks derived from subjective color scoring by human observers suggests that color scoring may utilize other cues and should thus be used cautiously.     

Metacognition and mentalizing are associated with distinct neural representations of decision uncertainty

Metacognition and mentalizing are both associated with meta-level mental state representations. Conventionally, metacognition refers to monitoring one’s own cognitive processes, while mentalizing refers to monitoring others’ cognitive processes. However, this self-other dichotomy is insufficient to delineate the 2 high-level mental processes. We here used functional magnetic resonance imaging (fMRI) to systematically investigate the neural representations of different levels of decision uncertainty in monitoring different targets (the current self, the past self [PS], and others) performing a perceptual decision-making task. Our results reveal diverse formats of internal mental state representations of decision uncertainty in mentalizing, separate from the associations with external cue information. External cue information was commonly represented in the right inferior parietal lobe (IPL) across the mentalizing tasks. However, the internal mental states of decision uncertainty attributed to others were uniquely represented in the dorsomedial prefrontal cortex (dmPFC), rather than the temporoparietal junction (TPJ) that also represented the object-level mental states of decision inaccuracy attributed to others. Further, the object-level and meta-level mental states of decision uncertainty, when attributed to the PS, were represented in the precuneus and the lateral frontopolar cortex (lFPC), respectively. In contrast, the dorsal anterior cingulate cortex (dACC) represented currently experienced decision uncertainty in metacognition, and also uncertainty about the estimated decision uncertainty (estimate uncertainty), but not the estimated decision uncertainty per se in mentalizing. Hence, our findings identify neural signatures to clearly delineate metacognition and mentalizing and further imply distinct neural computations on internal mental states of decision uncertainty during metacognition and mentalizing.

The relationship between metacognition and mentalizing is still a matter of debate, as both are associated with meta-representations. This study adapts a task paradigm used in metacognition to apply in mentalizing and compares the neural representations of decision uncertainty in metacognition and mentalizing.     

Clothing color mediates lizard responses to humans in a tropical forest

Identifying how ecotourism affects wildlife can lower its environmental impact. Human presence is an inherent component of ecotourism, which can impact animal behavior because animals often perceive humans as predators and, consequently, spend more time on human-directed antipredator behaviors and less on other fitness-relevant activities. We tested whether human clothing color affects water anole (Anolis aquaticus) behavior at a popular ecotourism destination in Costa Rica, testing the hypothesis that animals are more tolerant of humans wearing their sexually selected signaling color. We examined whether clothing resembling the primary signaling color (orange) of water anoles increases number of anole sightings and ease of capture. Research teams mimicked an ecotourism group by searching for anoles wearing one of three shirt treatments: orange, green, or blue. We conducted surveys at three different sites: a primary forest, secondary forest, and abandoned pasture. Wearing orange clothing resulted in more sightings and greater capture rates compared with blue or green. A higher proportion of males were captured when wearing orange whereas sex ratios of captured anoles were more equally proportional in the surveys when observers wore green or blue. We also found that capture success was greater when more people were present during a capture attempt. We demonstrate that colors “displayed” by perceived predators (i.e., humans) alter antipredator behaviors in water anoles. Clothing choice could have unintended impacts on wildlife, and wearing colors resembling the sexually selected signaling color might enhance tolerance toward humans.     

Effect of shape, size and color on selection of oviposition sites by Chaetorellia australis

The effect of shape, size and color on the selection of oviposition sites by females of Chaetorellia australis Hering (Diptera, Tephritidae) originating from infested yellow starthistle (YST) Centaurea solstitialis L. (Asteraceae, Cardueae) heads, was studied in the laboratory by direct observation of females sitting on or attempting to oviposit into different objects. Artificial substrates made of yellow-colored parafin was mimicking the natural oviposition sites (floral buds of YST), were used to study the effect of shape and size. The results revealed that spherical and conical objects of a total surface area of 310 mm², were visited more frequently than cylindrical and cubical ones of the same surface area. Also more females were observed and more oviposition attempts were recorded on spheres of 5 and 10 mm diameter than of 15 and 20 mm diameter. Yellow and orange dry YST heads, colored by dipping in molten colored ceresin wax, were preferred for oviposition to black, green, blue, red and white ones. The observed preference for certain colors depended primarily on the color hue and not on the intensity of the total reflected light. The females responded positively to hues reflecting maximally between 560 and 610 nm, optimum at 590 nm, while hues reflecting below 540 nm and especially between 400 and 500 nm appeared to have no positive effect.     

显微摄像条件对细胞形态测试结果的影响

目的:研究显微摄像条件对细胞形态测试结果的影响情况。方法:以苏木精-伊红(HE)染色的胃壁细胞为研究对象,分别在不同光亮度、对比度、饱和度和锐度的成像条件下进行显微摄像,采用图像分析软件(Image-Pro Plus 6.0)测试胃壁细胞的色度学和几何形态学参数,并对测试结果进行分析比较。结果:不同光亮度、对比度、饱和度组的胃壁细胞红、绿、蓝三基色差异均有统计学意义(P<0.05),其中红、绿、蓝基色值在高光亮度和高对比度组最高,同时红基色值在高饱和组最高,而绿、蓝基色值在高饱和组最低(P<0.05);不同锐度的胃壁细胞红、绿、蓝三基色差异没有统计学意义(P>0.05)。不同光亮度、对比度、饱和度和锐度的胃壁细胞的面积、周长、平均直径差异均没有统计学意义(P>0.05)。结论:光亮度、对比度和饱和度对细胞色度学参数影响明显,而对几何形态学参数无明显影响。