Risk of social colours in an agamid lizard: implications for the evolution of dynamic signals.

The forces of sexual and natural selection are typically invoked to explain variation in colour patterns of animals. Although the benefits of conspicuous colours for social signalling are well documented, evidence for their ecological cost, especially for dynamic colours, remains limited. We examined the riskiness of colour patterns of Psammophilus dorsalis, a species in which males express distinct colour combinations during social interactions. We first measured the conspicuousness of these colour patterns on different substrates based on the visual systems of conspecifics and predators (bird, snake, canid) and then quantified actual predation risk on these patterns using wax/polymer lizard models in the wild. The black and red male state exhibited during courtship was the most conspicuous to all visual systems, while the yellow and orange male aggression state and the brown female colour were least conspicuous. Models bearing the courtship colour pattern experienced the highest predator attacks, irrespective of the substrate they were placed on. Thus, social colours of males are not only conspicuous but also risky. Using physiological colours to shift in and out of conspicuous states may be an effective evolutionary solution to balance social signalling benefits with predation costs.

Context-dependent crypsis: a prey's perspective of a color polymorphic predator.

Many animals use body coloration as a strategy to communicate with conspecifics, prey, and predators. Color is a trade-off for some species, since they should be visible to conspecifics but cryptic to predators and prey. Some flower-dwelling predators, such as crab spiders, are capable of choosing the color of flowers where they ambush flower visitors and pollinators. In order to avoid being captured, visitors evaluate flowers visually before landing. The crab spider Mecaphesa dubia is a polymorphic species (white/purple color morphs), which inhabits the flower heads of a dune plant, Palafoxia lindenii. Using full-spectrum photography of spiders and flowers, we evaluated how honeybees perceived the spiders at different distances. Using visual modeling, we obtained the chromatic and achromatic contrasts of the spiders on flower heads as perceived by honeybees. Purple morphs were found mainly on the receptacle area and white morphs were equally likely to be found in the flowers and receptacle. According to theoretical modeling, white morphs were visible to honeybees from a distance of 10 cm in receptacle area but appeared to be cryptic in the flower area. Purple morphs were cryptic on the receptacle and less so when they were on the flowers. Spiders on flower heads are predicted to be more easily detected by honeybees using chromatic contrast. Our study shows that the conspicuousness of flower dwelling spiders to honeybees depends on the color morph, the distance of observation, and the position of spider on the flower head.

Spectral information as an orientation cue in dung beetles.

During the day, a non-uniform distribution of long and short wavelength light generates a colour gradient across the sky. This gradient could be used as a compass cue, particularly by animals such as dung beetles that rely primarily on celestial cues for orientation. Here, we tested if dung beetles can use spectral cues for orientation by presenting them with monochromatic (green and UV) light spots in an indoor arena. Beetles kept their original bearing when presented with a single light cue, green or UV, or when presented with both light cues set 180° apart. When either the UV or the green light was turned off after the beetles had set their bearing in the presence of both cues, they were still able to maintain their original bearing to the remaining light. However, if the beetles were presented with two identical green light spots set 180° apart, their ability to maintain their original bearing was impaired. In summary, our data show that ball-rolling beetles could potentially use the celestial chromatic gradient as a reference for orientation.

Cryptic differences in colour among Müllerian mimics: how can the visual capacities of predators and prey shape the evolution of wing colours?

Antagonistic interactions between predators and prey often lead to co-evolution. In the case of toxic prey, aposematic colours act as warning signals for predators and play a protective role. Evolutionary convergence in colour patterns among toxic prey evolves due to positive density-dependent selection and the benefits of mutual resemblance in spreading the mortality cost of educating predators over a larger prey assemblage. Comimetic species evolve highly similar colour patterns, but such convergence may interfere with intraspecific signalling and recognition in the prey community, especially for species involved in polymorphic mimicry. Using spectrophotometry measures, we investigated the variation in wing coloration among comimetic butterflies from distantly related lineages. We focused on seven morphs of the polymorphic species Heliconius numata and the seven corresponding comimetic species from the genus Melinaea. Significant differences in the yellow, orange and black patches of the wing were detected between genera. Perceptions of these cryptic differences by bird and butterfly observers were then estimated using models of animal vision based on physiological data. Our results showed that the most strikingly perceived differences were obtained for the contrast of yellow against a black background. The capacity to discriminate between comimetic genera based on this colour contrast was also evaluated to be higher for butterflies than for birds, suggesting that this variation in colour, likely undetectable to birds, might be used by butterflies for distinguishing mating partners without losing the benefits of mimicry. The evolution of wing colour in mimetic butterflies might thus be shaped by the opposite selective pressures exerted by predation and species recognition.

Deer management influences perception of avian plumage in temperate deciduous forests.

Many animals use visual signals to communicate; birds use colorful plumage to attract mates and repel intruders. Visual signal conspicuousness is influenced by the lighting environment, which can be altered by human-induced changes. For example, deer-management efforts can affect vegetation structure and light availability. Whether these changes alter animal communication is still unknown. We investigated the effect of deer management on forest light and the contrast of understory birds against the forest background. We modeled visual perception using: (1) an ultraviolet-sensitive (UVS) avian model and plumage parameters representative of red, yellow, and blue birds (2) species-specific turkey visual and plumage parameters, and (3) individual-specific brown-headed cowbird visual and plumage parameters. Deer management led to greater light irradiance and lowered forest background reflectance. Management increased chromatic contrasts in the UVS model, primarily in deciduous forests and low understory, and across all habitat types in turkey and cowbird models. Deer management did not affect achromatic contrasts in the UVS model, but was associated with lower contrast in mixed forests for turkeys and across habitats for cowbirds. Together, this suggests that management of deer browsing is likely to impact visual signaling for a wide range of avian species. However, we also suspect that species- and individual-specific parameters increased the resolution of models, warranting consideration in future studies. Further work should determine if differences in visual perception translate to biologically relevant consequences. Our results suggest that, at least for some species, deer browsing and anthropogenic change may impose an evolutionary driver on visual communication.

Visual Background Choice and Light Environment Affect Male Guppy Visual Contrast.

Male guppies (Poecilia reticulata) have multiple colored spots and perform courtship displays near the edges of streams in Trinidad in shallow water flowing through rainforest. Depending upon the orientation of the pair, the female sees the male displays against gravel or other stream bed substrates or against the spacelight-the roughly uniform light coming from the water column away from the bank. We observed courting pairs in two adjacent natural streams and noted the directions of each male display. We found that the female sees the male more often against spacelight than against gravel when females either faced the spacelight from the opposite bank or from downstream, or both. Visual modelling using natural substrate reflectances and field light measurements showed higher chromatic contrast of males against spacelight than against substrates independent of the two ambient light environments used during displays, but achromatic contrast depended upon the ambient light habitat. This suggests that courtship involves both chromatic and achromatic contrast. We conclude that the orientation of courting pairs and the ambient light spectrum should be accounted for in studies of mate choice, because the visual background and light affect visibility, and these differ with orientation.

Flower colour and size signals differ depending on geographical location and altitude region.

Bees are major pollinators of angiosperms and have phylogenetically conserved colour vision but differ in how various key species use achromatic information that is vital for both flower detection and size processing. We modelled green contrast and colour contrast signals from flowers of different countries where there are well established differences in availability of model bee species along altitudinal gradients. We tested for consistency in visual signals as expected from generalization in pollination principles using phylogenetically informed linear models. Patterns of chromatic contrast, achromatic green contrast and flower size differed among the three floras we examined. In Nepal there is a significant positive correlation between flower size and colour contrast in the subalpine region, but a negative correlation at the lower altitudes. At high elevations in Norway, where pollinators other than bees are common, flower size was positively correlated with colour contrast. At low and medium altitudes in Norway and in Australia, we did not observe a significant relationship between size and colour contrast. We thus find that the relationship between size, green and colour contrast cannot be generalized across communities, thus suggesting that flower visual signal adaptations to local pollinators are not limited to chromatic contrast.

The trade-off between color and size in lizards' conspicuous tails.

A tail of conspicuous coloration is hypothesized to be an advantageous trait for many species of lizards. Predator attacks would be directed to a non-vital, and autotomizable, body part, increasing the chance of survival. However, as body size increases it also increases the signaling area that could attract predators from greater distances, increasing the overall chance of predation. Here, we test the hypothesis that there is a trade-off between tail color and size, affecting predation probabilities. We used plasticine replicas of lizards to study the predation patterns of small and large lizards with red and blue tails. In a natural environment, we exposed six hundred replicas to the attacks of free-ranging predators. Large red-tailed replicas were more attacked by birds. Mammals and unidentified predators showed no preference for any size or colors. The attacks were not primarily directed to conspicuous tails when compared to the bodies/heads of our replicas. Our study suggests that red color signals in large lizards could enhance their detection by visually oriented predators (i.e., birds). The efficacy of conspicuous tails as a decoy may rely on associated behavioral displays, which are hard to test with static replicas.

A mathematical approach to assess the ability of light filters to improve color discriminability of color vision deficient persons.

Color vision deficiency (CVD) is a frequent condition that alters color perception to such an extent that many people encounter serious difficulties on their everyday lives. In this work, we present a strategy to analyze the effectiveness of light filters aimed to improve color discriminability of persons with CVD. The calculations are based on a simple model of color discrimination which has been successfully applied to several animal species. We first tested the calculations on three well-known commercial lenses designed for persons with CVD. In agreement with results of clinical studies, the calculations show that the highly colored lenses (VINO® and X-Chrom®) enhance chromaticity contrasts between problematic colors, whereas the more neutral Enchroma® do not provide any benefit. Also, we predict that two light filters proposed in recent works for novel lenses would not improve the performance of the commercial ones. Since the mathematical approach presented in this work enables predictive filter assessment, it opens the door to future research on the design of more effective lenses to improve color discriminability of persons with CVD. The calculations allow for large-scale screening of numerous light filters and different colored stimuli, CVD conditions, light sources, etc.

Color discrimination in anomalous trichromacy: Experiment and theory.

In anomalous trichromacy, the color signals available from comparing the activities of the two classes of cone sensitive in the medium and long wavelength parts of the spectrum are much reduced from those available in normal trichromacy, and color discrimination thresholds along the red-green axis are correspondingly elevated. Yet there is evidence that suprathreshold color perception is relatively preserved; this has led to the suggestion that anomalous trichromats post-receptorally amplify their impoverished red-green signals. To test this idea, we measured chromatic discrimination from white and from saturated red and green pedestals. If there is no post-receptoral compensation, the anomalous trichromat's loss of chromatic contrast will apply equally to the pedestal and to the test color. Coupled with a compressively nonlinear neural representation of saturation, this means that a given pedestal contrast will cause a smaller than normal modulation of discrimination sensitivity. We examined cases where chromatic pedestals impair the color discrimination of normal trichromatic observers. As predicted, anomalous observers experienced less impairment than normal trichromats, though they remained less sensitive than normal trichromats. Although the effectiveness of chromatic pedestals in impairing color discrimination was less for anomalous than for normal trichromats, the chromatic pedestals were more effective for anomalous observers than would be expected if the anomalous post-receptoral visual system were the same as in normal trichromacy; the hypothesis of zero compensation can be rejected. This might suggest that the effective contrast of the pedestal is post-receptorally amplified. But on closer analysis, the results do not support candidate simple models involving post-receptoral compensation either.

A contra-lateral comparison of the visual effects of a photochromic vs. non-photochromic contact lens.

PURPOSE: To compare the effects of a photochromic contact lens vs. a non-photochromic control lens on visual function. METHODS: A subject-masked, prospective contralateral eye design was used. Sixty-one subjects were enroled based on age (using a 2:1 allocation ratio for ages 18-39 and 40-65 years, respectively). The study lenses were senofilcon A with photochromic additive (Test) that filtered over the entire lens, compared to a non-photochromic Control with no tint. The Test lens was partially activated during testing with a steady-state transmittance of approximately 62%. Eligible subjects were tested using both study lenses, with Test and Control lens randomized by eye. Five visual function outcomes were tested: photostress recovery (PSR), glare disability (GD), glare discomfort (GDC), chromatic contrast (CC) and vernier acuity (VA). Iris colour and macular pigment density were assessed as control variables. PSR was measured as the time needed to recover sight of a target after an intense xenon flash exposure; GD was evaluated as the energy needed to veil a central target by a surrounding xenon annulus; GDC was measured using bio-imaging of the squint response and by self-report using a 9-item Likert scale; CC was measured as thresholds for a yellow grating target superposed on a 460-nm background; VA was determined by measuring vernier offsets of light lines through apertures. RESULTS: Based on our stimulus conditions, PSR was 43% faster using the Test vs. the Control. The eye wearing the Test had 38% less squint (GDC) compared to the Control. GD was improved by 36% in the Test vs. Control and CC was enhanced by 48% with the Test. There was no significant difference in VA. CONCLUSIONS: There was a beneficial influence on visual function when comparing the photochromic with the non-photochromic contact lens. This benefit was seen specifically with respect to PRT, GDC, GD and CC thresholds.

Effect of chromatic contrast on stereoacuity measurement with computer-aided three-dimensional technology.

BACKGROUND: Various measurement tools are utilized to detect the stereopsis threshold in the clinic, but seldom of these involves chromatic information. Incorporating colorful elements into computer-aided, three-dimensional (3D) evaluation systems could help the tests appear more vivid and attractive. The aim of this study was to clarify the effect of different chromatic pair stereo targets on the stereoacuity result. METHODS: A total of 17 subjects with visual acuity in each eye of at least 0 logarithmic minimum angle of resolution (logMAR) and a stereoacuity of at least 32 second of arc (arcsec) were recruited. A 3D laptop with liquid crystal shutter glasses was used for evaluating stereoacuity. Thirteen pages were set including seven maximum color contrast pages and six isoluminant color contrast pages. RESULTS: In maximum color contrast pair, no significant difference was found among all seven experiments [six test groups and one reference group, one-way analysis of variance (ANOVA) test, F=0.995, P=0.493]. There was also no significant difference among the isoluminant color contrast pairs (six test groups, one-way ANOVA test, F=0.873, P=0.644). Paired t-test was used for comparing the data between the same hue series in the maximum color contrast pair vs. the isoluminant color contrast pair, and significant differences were found in all six pairs (P<0.001). CONCLUSIONS: Adding chromatic factors to the stereo test is practical to evaluate stereopsis.

Testing a key assumption in animal communication: between-individual variation in female visual systems alters perception of male signals.

Variation in male signal production has been extensively studied because of its relevance to animal communication and sexual selection. Although we now know much about the mechanisms that can lead to variation between males in the properties of their signals, there is still a general assumption that there is little variation in terms of how females process these male signals. Variation between females in signal processing may lead to variation between females in how they rank individual males, meaning that one single signal may not be universally attractive to all females. We tested this assumption in a group of female wild-caught brown-headed cowbirds (Molothrus ater), a species that uses a male visual signal (e.g. a wingspread display) to make its mate-choice decisions. We found that females varied in two key parameters of their visual sensory systems related to chromatic and achromatic vision: cone densities (both total and proportions) and cone oil droplet absorbance. Using visual chromatic and achromatic contrast modeling, we then found that this between-individual variation in visual physiology leads to significant between-individual differences in how females perceive chromatic and achromatic male signals. These differences may lead to variation in female preferences for male visual signals, which would provide a potential mechanism for explaining individual differences in mate-choice behavior.

A generalized equation for the calculation of receptor noise limited colour distances in n-chromatic visual systems.

Researchers must assess similarities and differences in colour from an animal's eye view when investigating hypotheses in ecology, evolution and behaviour. Nervous systems generate colour perceptions by comparing the responses of different spectral classes of photoreceptor through colour opponent mechanisms, and the performance of these mechanisms is limited by photoreceptor noise. Accordingly, the receptor noise limited (RNL) colour distance model of Vorobyev and Osorio (Vorobyev & Osorio 1998 Proc. R. Soc. Lond. B265, 351-358 (doi:10.1098/rspb.1998.0302)) generates predictions about the discriminability of colours that agree with behavioural data, and consequently it has found wide application in studies of animal colour vision. Vorobyev and Osorio (1998) provide equations to calculate RNL colour distances for animals with di-, tri- and tetrachromatic vision, which is adequate for many species. However, researchers may sometimes wish to compute RNL colour distances for potentially more complex colour visual systems. Thus, we derive a simple, single formula for the computation of RNL distance between two measurements of colour, equivalent to the published di-, tri- and tetrachromatic equations of Vorobyev and Osorio (1998), and valid for colour visual systems with any number of types of noisy photoreceptors. This formula will allow the easy application of this important colour visual model across the fields of ecology, evolution and behaviour.

Defective chromatic and achromatic visual pathways in developmental dyslexia: Cues for an integrated intervention programme.

PURPOSE: As well as obtaining confirmation of the magnocellular system involvement in developmental dyslexia (DD); the aim was primarily to search for a possible involvement of the parvocellular system; and, furthermore, to complete the assessment of the visual chromatic axis by also analysing the koniocellular system. METHODS: Visual evoked potentials (VEPs) in response to achromatic stimuli with low luminance contrast and low spatial frequency, and isoluminant red/green and blue/yellow stimuli with high spatial frequency were recorded in 10 dyslexic children and 10 age- and sex-matched, healthy subjects. RESULTS: Dyslexic children showed delayed VEPs to both achromatic stimuli (magnocellular-dorsal stream) and isoluminant red/green and blue/yellow stimuli (parvocellular-ventral and koniocellular streams). To our knowledge, this is the first time that a dysfunction of colour vision has been brought to light in an objective way (i.e., by means of electrophysiological methods) in children with DD. CONCLUSION: These results give rise to speculation concerning the need for a putative approach for promoting both learning how to read and/or improving existing reading skills of children with or at risk of DD. The working hypothesis would be to combine two integrated interventions in a single programme aimed at fostering the function of both the magnocellular and the parvocellular streams.

The effects of photochromic lenses on visual performance.

BACKGROUND: The purpose of the current study was to evaluate the effects of filtering by an activated photochromic lens on visual performance in healthy adults. Glare disability, glare discomfort, heterochromatic contrast thresholds and photostress recovery time were assessed. METHODS: A subject-masked, randomised, cross-over design was employed. Seventy-five healthy adults were recruited, aged 19 to 73 years (mean = 45.61 ± 13.24 years). Visual functions were measured using three different photochromic lenses that were partially activated with a steady state transmittance of 63 per cent T (Gray1), 71 per cent T (Gray2), and 71 per cent T (Brown). These lenses were compared with a clear (92 per cent transmission) polycarbonate lens. Glare disability was assessed as the intensity of a white (xenon)-light annulus necessary to obscure a central grating target. Heterochromatic contrast thresholds were measured as absolute thresholds for a monochromatic 570 nm target superimposed on a 460 nm circular background. Glare discomfort was quantified using bio-imaging of the squint response as well as a Likert-based self-report scale. Photostress recovery time was recorded as the time necessary to regain sight of a grating target after intense light exposure. Glare discomfort and photostress recovery were only assessed for the Gray1 lens compared to placebo. Lens order was randomised between subjects and conditions. RESULTS: All visual functions measured were significantly improved (p < 0.05) for all of the activated photochromic lenses tested versus the clear lens. In the glare disability and heterochromatic contrast conditions, numeric differences (p < 0.09) were also seen between each of the three different activated photochromic lens types. Glare discomfort and photostress recovery times were improved in the Gray1 condition, as quantified by both the squint and subjective responses (p < 0.05). CONCLUSION: Adding filtering via a photochromic lens significantly increased subjects' abilities to cope with intense broadband and shortwave lighting conditions and to adapt back to normal viewing after being presented with an intense photostressor.

Longitudinal measurements of luminance and chromatic contrast sensitivity: comparison between wavefront-guided LASIK and contralateral PRK for myopia / Medidas longitudinais da sensibilidade ao contraste de luminância e cromático: comparação entre wavefront-LASIK e wavefront-PRK para miopia

PURPOSE: The present study aimed to compare the postoperative contrast sensitivity functions between wavefront-guided LASIK eyes and their contralateral wavefront-guided PRK eyes. METHODS: The participants were 11 healthy subjects (mean age=32.4 ± 6.2 years) who had myopic astigmatism. The spatial contrast sensitivity functions were measured before and three times after the surgery. Psycho and a Cambridge graphic board (VSG 2/4) were used to measure luminance, red-green, and blue-yellow spatial contrast sensitivity functions (from 0.85 to 13.1 cycles/degree). Longitudinal analysis and comparison between surgeries were performed. RESULTS: There was no significant contrast sensitivity change during the one-year follow-up measurements neither for LASIK nor for PRK eyes. The comparison between procedures showed no differences at 12 months postoperative. CONCLUSIONS: The present data showed similar contrast sensitivities during one-year follow-up of wave-front guided refractive surgeries. Moreover, one year postoperative data showed no differences in the effects of either wavefront-guided LASIK or wavefront-guided PRK on the luminance and chromatic spatial contrast sensitivity functions.

OBJETIVO: A proposta do presente estudo é comparar funções de sensibilidade ao contraste obtidas após wavefront-LASIK e wavefront-PRK no olho contralateral. MÉTODOS: Os participantes foram 11 sujeitos saudáveis (idade média=32,4 ± 6,2 anos) com astigmatismo miópico. As funções de sensibilidade ao contraste espacial foram obtidas antes e três vezes após a cirurgia. O programa Psycho e uma placa gráfica da Cambridge Research Systems (VSG 2/4) permitiram gerar os estímulos com contraste espacial de luminância e cromático (verde-vermelho e azul-amarelo) de 0,85 até 13,1 ciclos/grau. Análises longitudinais e comparações entre as cirurgias foram realizadas. RESULTADOS: Não houve mudança significativa da sensibilidade ao contraste durante o primeiro ano após a cirurgia para o olho que recebeu o LASIK ou para o olho que recebeu o PRK. A comparação entre as cirurgias também foi semelhante no pós-operatório de um ano. CONCLUSÕES: Os resultados apresentados mostraram sensibilidade ao contraste semelhante durante o primeiro ano após a cirurgia refrativa com o wavefront. Além disso, no pós-operatório de um ano não houve diferença nas funções de sensibilidade ao contraste de luminância e cromático entre os olhos que receberam LASIK e os que receberam PRK.