Colour constancy from temporal cues: better matches with less variability under fast illuminant changes

Ratios of excitations in each cone-photoreceptor class produced by light reflected from pairs of surfaces in a scene are almost invariant under natural illuminant changes. The stability of these spatially defined ratios may explain the remarkable ability of human observers to efficiently discriminate illuminant changes from changes in surface reflectances. Spatial cone-excitation ratios are not, however, exactly invariant. This study is concerned with observers' sensitivity to these invariance violations. Simulations of Mondrian paintings with either 49 or two natural surfaces under Planckian illuminants were presented as images on a computer-controlled display in a two-interval experimental design: in one interval, the surfaces underwent an illuminant change; in the other interval, the surfaces underwent the same change but the images were then corrected so that, for each cone class, ratios of excitations were preserved exactly. Although the intervals with corrected images corresponded individually to highly improbable natural events, observers systematically misidentified them as containing the illuminant changes, the probability of error increasing as the violation of invariance in the other interval increased. For the range of illuminants and surfaces tested, sensitivity to violations of invariance was found to depend on cone class: it was greatest for long-wavelength-sensitive cones and least for short-wavelength-sensitive cones. Spatial cone-excitation ratios, or some closely related quantities, seem to be the cues preferred by observers for making inferences about surface illuminant changes.

Colour constancy assessed by asymmetric simultaneous colour matching usually reveals limited levels of performance in the unadapted eye. Yet observers can readily discriminate illuminant changes on a scene from changes in the spectral reflectances of the surfaces making up the scene. This ability is probably based on judgements of relational colour constancy, in turn based on the physical stability of spatial ratios of cone excitations under illuminant changes. Evidence is presented suggesting that the ability to detect violations in relational colour constancy depends on temporal transient cues. Because colour constancy and relational colour constancy are closely connected, it should be possible to improve estimates of colour constancy by introducing similar transient cues into the matching task. To test this hypothesis, an experiment was performed in which observers made surface-colour matches between patterns presented in the same position in an alternating sequence with period 2 s or, as a control, presented simultaneously, side-by-side. The degree of constancy was significantly higher for sequential presentation, reaching 87% for matches averaged over 20 observers. Temporal cues may offer a useful source of information for making colour-constancy judgements.

Knowing when an event is likely to occur allows attentional resources to be oriented toward that moment in time, enhancing processing of the event. We previously found that children (mean age 11 years) are unable to use endogenous temporal cues to orient attention in time, despite being able to use endogenous spatial cues (arrows) to orient attention in space. Arrow cues, however, may have proved beneficial by engaging exogenous (automatic), as well as endogenous (voluntary), orienting mechanisms. We therefore conducted two studies in which the exogenous properties of visual temporal cues were increased, to examine whether this helped children orient their attention in time. In the first study, the location of an imperative target was predicted by the direction of a left or right spatial arrow cue while its onset was predicted by the relative duration of a short or long temporal cue. To minimize the influence of rhythmic entrainment in the temporal condition, the foreperiod (500 ms/1100 ms) was deliberately chosen so as not to precisely match the duration of the temporal cue (100 ms/400 ms). Targets appeared either at cued locations/onset times (valid trials) or at unexpected locations/onset times (invalid trials). Adults’ response times were significantly slower for invalid versus valid trials, in both spatial and temporal domains. Despite being slowed by invalid spatial cues, children (mean age 10.7 years) were unperturbed by invalid temporal cues, suggesting that these duration-based temporal cues did not help them orient attention in time. In the second study, we enhanced the exogenous properties of temporal cues further, by presenting multiple temporal cues in an isochronous (rhythmic) sequence. Again, to minimize automatic entrainment, target onset did not match the isochronous interval. Children (mean age 11.4 years), as well as adults, were now significantly slowed by invalid cues in both the temporal and spatial dimension. The sequential, as opposed to single, presentation of temporal cues therefore helped children to orient their attention in time. We suggest that the exogenous properties of sequential presentation provide a temporal scaffold that supports the additional attentional and mnemonic requirements of temporal, as compared to spatial, processing.

The purpose of the present study is to systematically replicate and extend the procedures of Kern and Marder (1996) using simultaneous and sequential presentations of preferred and nonpreferred foods. Systematic fading procedures were evaluated to decrease the amount of preferred foods and increase the amount of nonpreferred foods presented. The participants were two 16-year-old males diagnosed with autism that had a history of food selectivity. In the simultaneous presentation, preferred foods were presented at the same time as nonpreferred foods. In the sequential presentation, acceptance of the nonpreferred food resulted in the presentation of the preferred food. Results were evaluated using an alternating treatments design to compare the two interventions (simultaneous presentation vs. sequential presentation). Increases in consumption occurred immediately in the simultaneous and sequential presentations for Participant 1 and in the sequential presentation for Participant 2. Additional treatment interventions were evaluated for Participant 2 in the simultaneous presentation because consumption did not increase.

Invariance of surface color representations across illuminant changes in the human cortex

We investigated several sensory and cognitive determinants of colour constancy across 40 illumination hues. In the first experiment, we measured colour naming for the illumination and for the colour induced by the illumination on the colorimetric grey. Results confirmed that the induced colours are approximately complementary to the colour of the illumination. In the second experiment, we measured colour constancy using achromatic adjustments. Average colour constancy was perfect under the blue daylight illumination and decreased in colour directions away from the blue daylight illumination due to undershooting and a strong blue bias. Apart from this blue bias, colour constancy was not related to illumination discrimination and to chromatic detection measured previously with the same setup and stimuli. We also observed a strong negative relationship between the degree of colour constancy and the consensus of naming the illumination colour. Constancy coincided with a low naming consensus, in particular because bluish illumination colours were sometimes seen as achromatic. Blue bias and category consensus alone explained >68%, and all determinants together explained >94% of the variance of achromatic adjustments. These findings suggest that colour constancy is optimised for blue daylight.

We have examined visual functions, including colour vision, in a patient with bilateral cortical lesions involving mainly the fusiform and lingual gyri, areas known to be involved in the central processing of chromatic stimuli. The patient has near normal (6/9) acuity, and his responses to tests of binocular function and spatial vision are normal, as are his discrimination of changes in target speed and surface lightness. He does, however, exhibit minor losses in the upper visual field, mild prosopagnosia and topographical agnosia, all conditions commonly associated with cerebral achromatopsia. Colour matches and spectral response data establish that his cone photoreceptors have normal spectral characteristics and his spectral sensitivity measured against a white background reveals normal postreceptoral chromatic function. The patient's colour discrimination for differences in wavelength, hue or saturation is, however, impaired and his colour naming is significantly disturbed, particularly for blues and greens. We have determined the areas of the chromaticity chart that correspond to his naming categories for surface colours, and show that changes in illuminant cause him to alter the names of surface colours in a manner consistent with the changes in their chromaticities. Other subjects with normal or congenital red-green deficient colour vision make many fewer name changes under changes in illuminant. We conclude that the patient's colour constancy is impaired as a consequence of abnormal central processing of colour vision.

The equivalence of tactilely explored and visually perceived objects is well known (Gibson, 1969, 215-231). Similar tactile-visual equivalence occurs with passive tactile input, as in backwriting (Neisser, 1967, 46-85). It is difficult to find systematic explorations of tactile-visual equivalence with the tactile standard passively presented. The present study initiated such systematic exploration. A younger (2to 4-yr.-old, n = 8 ) and an older (7to 13-yr.-old, n = 11) group of children were each presented, in varying order, matching-to-sample tasks requiring discrimination between mirror-image oblique lines oriented 45 to the right vs left or between a triangle vs circle. The stimulus chosen from a given pair to be the standard was presented either visually, or by tactile drawing on a cloth template placed on the back. Tactile and visual stimuli were identical in size, shape, and orientation. Sequential stimulus presentation in the tactile mode by drawing on the back was used instead of simply pressing the stimulus on S's back in order to preserve the analogy between our passive presentation and the more commonly used active sequential search procedure. Matching was always done by selecting one of the visually presented pair. The standard was varied randomly from trial to trial. For the oblique line condition, stimulus locus was varied; either the right, left or middle of the back being used on a given trial. Further, a guess rate was obtained for each stimulus pair by eliminating presentation of the standard on certain trials. The older group made no errors when the standard was visually presented and never made more than 8% errors with a tactile standard. Their guess-rates were at chance levels. The younger group made no errors when the visually presented standard was from the triangle-circle pair but performed at only 74% correct when the visually presented standard was from the mirror-image pair. A Mann-Whitney U test showed this difference as a function of stimulus type to be significant ( p < .02). Younger Ss performed at levels significantly below (largest p < .01) those of older Ss under all conditions except the above mentioned visual-visual, triangle-circle matching task. However, the younger group performed above (largest fi < .03) the guess-rate on all but two of the tasks, viz., tactile-visual matching of oblique lines when presented to the left and when presented to the middle of the back. The latter tasks resulted in high inter-subject variability, some Ss performing above chance and others choosing the mirror-image of the standard. Thus, the well-known tendency for young children to have difficulty discriminating visually presented mirror-image stimuli also occurs when mirror-image stimuli are drawn on S's back. The development of ability to discriminate passively received tactile stimuli parallels that previously reported for tactile stimuli which were actively explored (Rudel & Teuber, 1964). In light of the great emphasis which has been placed on the role of active exploratory movement in the development of tactile perception (e.g., Rudel & Teuber, 1964), the above-chance performances of Ss in the younger group are particularly interesting.

This study examines a wide range of numerical representations (i.e., quantity, knowledge of multiplication facts, and use of parity information) in adult deaf signers. We introduce a modified version of the number bisection task, with sequential stimulus presentation, which allows for a systematic examination of mathematical skills in deaf individuals in different modalities (number signs in streaming video vs. Arabic digit displays). Reaction times and accuracy measures indicated that deaf signers make use of several representations simultaneously when bisecting number triplets, paralleling earlier findings in hearing individuals. Furthermore, some differences were obtained between the 2 display modalities, with effects being less prominent in the Arabic digit mode, suggesting that mathematical abilities in deaf signers should be assessed in their native sign language.

Recent studies have highlighted the fact that some tasks used to study symbolic number representations are confounded by judgments about physical similarity. Here, we investigated whether the contribution of physical similarity and numerical representation differed in the often-used symbolic same-different, numerical comparison, physical comparison, and priming tasks. Experiment 1 showed that subjective physical similarity was the best predictor of participants' performance in the same-different task, regardless of simultaneous or sequential presentation. Furthermore, the contribution of subjective physical similarity was larger in a simultaneous presentation than in a sequential presentation. Experiment 2 showed that only numerical representation was involved in numerical comparison. Experiment 3 showed that both subjective physical similarity and numerical representation contributed to participants' physical comparison performance. Finally, only numerical representation contributed to participants' performance in a priming task as revealed by Experiment 4. Taken together, the contribution of physical similarity and numerical representation depends on task demands. Performance primarily seems to rely on numerical properties in tasks that require explicit quantitative comparison judgments (physical or numerical), while physical stimulus properties exert an effect in the same-different task.

Event Abstract Back to Event The effect of surface material on colour constancy in real world scenes Annette Werner1* and Lara Zebrowski1, 2 1 Tübingen University, Ophthalmology, Germany 2 Ophthalmology, Germany The visual appearance of real world objects depends on their reflectance properties, illumination and geometrical factors. We asked how human colour constancy performance deals with the depth-mesostructure of surfaces, which may provide additional cues or, alternatively, worsen colour constancy. In our experiments we presented samples (circular patches, 90 mm) of different materials (paper, fur, tile, cloth, leather), each mounted on a black sample holder (front 30 x 15 cm, 60 deg slope) and presented in the middle of a black viewing box (1.0 x 1.0 x 0.8 m). All samples appeared nearly achromatic under daylight. The samples and the box were illuminated by a computer controlled, calibrated LCD-projector (Panasonic PT AE 1000E) which was mounted above the observers' head. The observers (2 male, 2 female) viewed the samples frontally (viewing distance 90 cm). The chromaticity of the standard illuminant was D65, the equiluminant test-illuminants were chosen from one of the cardinal axes. After viewing the samples under the standard illuminant for 15 s, the respective test-illuminant was presented for 5 s. Colour constancy was quantified by a hue-cancellation method, whereby the observer adjusts the appearance of the sample so that it appears achromatic (“gray”) under the respective test illuminant. Colour constancy for the different materials was found not to differ significantly, but there was a trend for compensating illumination changes best for fur and worst for tile surfaces, across all illuminants and observers, with paper ranking in the middle. The possible role of depth-mesostructure as a cue for colour constancy is discussed. Acknowledgements Supported by BMBF grant FKZ 01GQ1002. Keywords: colour constancy, material &amp, surfaces, mesostructure, Perception Conference: Bernstein Conference 2012, Munich, Germany, 12 Sep - 14 Sep, 2012. Presentation Type: Poster Topic: Sensory processing and perception Citation: Werner A and Zebrowski L (2012). The effect of surface material on colour constancy in real world scenes. Front. Comput. Neurosci. Conference Abstract: Bernstein Conference 2012. doi: 10.3389/conf.fncom.2012.55.00051 Copyright: The abstracts in this collection have not been subject to any Frontiers peer review or checks, and are not endorsed by Frontiers. They are made available through the Frontiers publishing platform as a service to conference organizers and presenters. The copyright in the individual abstracts is owned by the author of each abstract or his/her employer unless otherwise stated. Each abstract, as well as the collection of abstracts, are published under a Creative Commons CC-BY 4.0 (attribution) licence (https://creativecommons.org/licenses/by/4.0/) and may thus be reproduced, translated, adapted and be the subject of derivative works provided the authors and Frontiers are attributed. For Frontiers’ terms and conditions please see https://www.frontiersin.org/legal/terms-and-conditions. Received: 25 May 2012; Published Online: 12 Sep 2012. * Correspondence: Dr. Annette Werner, Tübingen University, Ophthalmology, Tübingen, 72070, Germany, annette.werner@uni-tuebingen.de Login Required This action requires you to be registered with Frontiers and logged in. To register or login click here. Abstract Info Abstract The Authors in Frontiers Annette Werner Lara Zebrowski Google Annette Werner Lara Zebrowski Google Scholar Annette Werner Lara Zebrowski PubMed Annette Werner Lara Zebrowski Related Article in Frontiers Google Scholar PubMed Abstract Close Back to top Javascript is disabled. Please enable Javascript in your browser settings in order to see all the content on this page.

Perception of colour depends on the spectral composition of light that reaches retina and depends as well on various mechanisms of visual system that processes information flow. The few important mechanisms can be distinguished in colour perception: colour adaptation, colour constancy and colour contrast. If the visual field has only one coloured object, then colour perception will be determined by spectral composition of the light and colour adaptation. Whereas mechanisms of colour constancy and colour contrast switches on when in the visual field there are at least two colour objects. Von Kries (1905) have attributed colour constancy phenomenon to theory of receptoral adaptation. But this is theory is applicable to local processes happening in relatively small size of visual field. Craven and Foster (1992) shows that receptor excitation ratios remains constant during change of illumination. But again remains unexplained colour change during adaptation. So, the hypothesis is raised that two processes attribute colour perception: local colour contrast calculation and global adaptation to the background. Therefore the experiments have been carried out to establish the colour contrast and background adaptation impact on colour perception.Four subjects with normal colour vision participated in the experiments. 40 Munsell samples (value 7 and chroma 4) illuminated with one reference illuminant (standard C) and 6 test illuminants (standard A, standard S, cardinal red, cardinal green, cardinal yellow and cardinal blue) were simulated on computer monitor. The dark-adapted subjects have been shown colour samples on neutral background illuminated with one of test illuminants. The task was to match the colour stimuli appearance under reference illuminant. The sequential asymmetric matching procedure was carried out. First subject adapts to neutral background under illuminan C then test stimulus and test background appears for limited time followed by readaptation to neutral background. Then subject is asked to adjust the colour mach under illuminant C. Two different experiment paradigms have been used. In the first one the stimulus had 2° on neutral background covering 20° of visual field. In the second paradigm the stimulus size was the same but the background was covering the all visual field. The adaptation and presentation timings were 1, 5, 30 or 60 seconds.Results under the first experiment paradigm show partial colour constancy for all subjects and for all test illuminants under various adaptation times. Despite quite a long adaptation time of 30 seconds subjects was unable to achieve full colour constancy. Colour constancy improves under second experiment paradigm. 60-second adaptation time is enough to achieve full colour constancy. The less adaptation time (1 or 30 second) gives partial colour constancy.The subject sees two colours (stimulus and background) during the experiment. The colour perception of stimulus and background changes during adaptation time. In the first 5 seconds of adaptation 40–60% of full adaptation level is reached (Fairchild and Reniff, 1995; Werner et al., 2000). Wesner and Shevell (1992, 1994) shown that signals from all visual field have influence on colour perception of object. The first part of our experiment shows that neutral background of 20° gives partial adaptation to background colour. Therefore, increase background illumination to full visual field gives full adaptation to background. So, subject perceives different coloured background under various illuminants as the same neutral (grey) background.We can state that two different systems have been distinguished in the process of colour perception. One system evaluates the colour difference between the stimulus and the background. Second system evaluates the colour of the background. Perceived colour difference during adaptation does not change much, but perceived colour of the background changes a lot and drifts towards neutral colour. The hypothesis of two level colour perception is supported by experimental data.&#x0D;

Color constancy refers to the ability of the human visual system to stabilize the color appearance of surfaces under an illuminant change. In this work we studied how the interrelations among nine colors are perceived under illuminant changes, particularly whether they remain stable across 10 different conditions (5 illuminants and 2 backgrounds). To do so we have used a paradigm that measures several colors under an immersive state of adaptation. From our measures we defined a perceptual structure descriptor that is up to 87% stable over all conditions, suggesting that color category features could be used to predict color constancy. This is in agreement with previous results on the stability of border categories [1,2] and with computational color constancy algorithms [3] for estimating the scene illuminant.

One proposed mechanism for underpinning colour constancy is computation of the relative activity of cones within one class--cone ratios, or cone contrasts--between surfaces in a fixed scene undergoing a change in illuminant. Although there is evidence that cone ratios do determine colour appearance under many conditions, the site or sites of their computation is unknown. Here, we report that a cerebrally achromatopsic observer, MS, displayed evidence of colour constancy in asymmetric colour matching tasks and was able to discriminate changes in cone ratios for simple, but not complex scenes. We hypothesise that the site of local cone-ratio computation is therefore early in the visual system, probably retinal.

Color constancy is the ability to assign a constant color to an object independent of changes in illumination. Color constancy is achieved by taking context information into account. Previous approaches that have used matching paradigms to quantify color constancy found degrees of constancy between 20% and 80%. Here, we studied color constancy in a color-naming task under different conditions of surround illumination and patch size. Observers categorized more than 400 patches for each illumination condition. This allows one to overcome inherent limitations in color naming and to study the changes in color categories under illumination changes. When small central test patches with a full context illumination were categorized, observers followed the illumination shift almost completely, showing a high degree of constancy (99%). Reducing the available context information or increasing the patch size decreased the degree of constancy to about 50%. Moderate degrees of constancy (66%) occurred even when the test patches were never viewed simultaneously but only in temporal alternation with the illumination. Boundaries between color categories were largely stable within and across observers under neutral illumination. Under changing illumination, there were small but systematic variations in the color category boundaries. Color category boundaries tended to rotate away from the illumination color. This variation was largest under full context conditions where highest degrees of color constancy were obtained.