The term “color constancy” is often used to describe the phenomenon of stable color appearance of surfaces with changing illumination (Jameson & Hurvich,
1989; Kaiser & Boynton,
1996). This formulation of color constancy refers directly to human perceptual experience. However, quantitative measurements of color constancy under various experimental conditions have shown that human color constancy is far from perfect (Arend & Reeves,
1986; Kraft & Brainard,
1999; Kuriki & Uchikawa,
1996). Several explanations have been suggested that may account for this imperfect performance, including effects of instruction (Arend & Reeves,
1986), inappropriateness of the stimuli used (Kraft & Brainard,
1999), increment–decrement asymmetries (Bäuml,
2001), and the size of the illuminant shift (Craven & Foster,
1992).
Psychophysical methods such as achromatic settings or asymmetric matching promise accurate, quantitative assessment of color constancy. It is not clear how well such tasks characterize the stability of observer's color appearance across the full range of surface colors. However, although spatial or temporal asymmetric matching can be used to characterize perception of colors away from the neutral point, recent results suggest that it might be inappropriate to evaluate human color constancy for a variety of reasons (Foster,
2003; Logvinenko & Maloney,
2006; Maloney,
1999). In particular, when observers are asked to set a test surface under a given illumination so that it appears perceptually indistinguishable to a reference patch under a second illumination, they sometimes report that they cannot find a satisfying setting. This problem was first noted by David Katz, who reported that when observers make a match in a lightness or color constancy experiment, there is usually a residual difference (Katz,
1911, p. 82). The following comment from a recent asymmetric color matching study may illustrate this problem:
At this match point, however, the test and the match surfaces looked different, and the observers felt as if further adjustments of the match surface should produce a better correspondence. Yet turning any of the knobs or combinations of knobs only increased the perceptual difference (Brainard, Brunt, & Speigle, 1997, p. 2098).
If asymmetric matches do not, in fact, match, then it is questionable whether they can be used to characterize color constancy.
Achromatic setting measures, for example, essentially measure only the location of the observer's neutral point, and their use to characterize color appearance away from the neutral point involves assumptions. Speigle and Brainard (
1999) report, for example, that achromatic settings can be used to predict asymmetric matches, but, as just noted, it is unclear whether the latter can be used to measure stability of color appearance under changes in illumination.
A task that is more directly related to the purpose of color constancy in terms of object recognition is color categorization (Boynton & Olson,
1987). The grouping of colors into a small number of discrete categories seems to be a universal feature of the visual system (Kay & Regier,
2003). Jameson and Hurvich (
1989) argue that color categories of objects are preserved with changes of the illuminant, if one takes compensatory mechanisms like chromatic adaptation into account. Troost and deWeert (
1991) investigated the color constancy performance of observers in a color categorization task and asymmetric matchings. They found that observers reliably used the same color category for a test patch with changes of the illumination. Although color categorization seems to be a reliable and appropriate measure of human color constancy, two disadvantages of this task are the lack of comparability of the color categorization data to quantitative measures and the potential that the conclusions drawn depend on an arbitrary choice of categories.
In this study, we introduce hue scaling as an alternative method to investigate color constancy (Abramov & Gordon,
1994; Boynton & Gordon,
1965). On one hand, this task is evidently based on judgments of the appearance of chromatic surfaces under varying illumination and is therefore appropriate to study human color constancy. On the other hand, the resulting data are potentially comparable to quantitative measures of color constancy. Moreover, with the usage of a hue scaling task, we hope to eliminate disadvantages that are inherent in asymmetric matchings and achromatic settings. We also test a generalization of the model proposed by Speigle and Brainard (
1999) to link achromatic settings and asymmetric matching but in the context of hue scaling. Specifically, we test whether knowledge of the hue scalings of a single test patch under two lights can be used to predict scaling of all test patches under these two lights. We will describe their model and our tests in more detail in the
Data analysis section of the first experiment.
Previous studies of color constancy have employed stimuli consisting of patterns of flat surfaces embedded in a fronto-parallel plane, often called “Mondrians” (Land & McCann,
1971). A disadvantage of this configuration is that more complex light–surface interactions are not taken into account (Boyaci, Doerschner, Snyder, & Maloney,
2006). Moreover, reported indices of color constancy are typically low. In the experiments reported here, we used simulated three-dimensional (3D) stimuli presented binocularly to more closely approximate natural viewing conditions (Boyaci et al.,
2006; Boyaci, Maloney, & Hersh,
2003; Maloney,
1999). These scenes contain additional cues to the illuminant such as specular highlights or shadows. The use of these enriched stimuli was also motivated by the idea that the visual system seems to combine cues that are available in a scene to estimate the illuminant (Boyaci, Doerschner, & Maloney,
2006; Kraft & Brainard,
1999; Snyder, Doerschner, & Maloney,
2005; Yang & Maloney,
2001).
In addition to the cues presented in a scene, chromatic adaptation plays a crucial role in the adjustment of the visual system to the illuminant (Kuriki & Uchikawa,
1996). Studies of the time course of chromatic adaptation have revealed that this process consists of a fast and a slow phase of adaptation (Fairchild & Reniff,
1995; Rinner & Gegenfurtner,
2000). The slow phase of adaptation might be related to slow changes of daylights that occur in the daytime. In
Experiment 2 of this study, we were able to demonstrate, by accident, the strength of the isolated slow adaptation mechanism.