Visual mode switching: Improved general compensation for environmental color changes requires only one exposure per day.

When the visual environment changes, vision adapts in order to maintain accurate perception. For repeatedly encountered environmental changes, the visual system may learn to adjust immediately, a process called "visual mode switching." For example, following experience with red glasses, participants report that the glasses' redness fades instantly when they put the glasses on. Here we tested (1) whether once-daily experience suffices for learning to switch visual modes and (2) whether effects of mode switching apply to most stimuli affected by the environmental change. In Experiment 1, 12 participants wore bright red glasses for a single 5-hr period each day for 5 days, and we tested for changes in the perception of unique yellow, which contains neither red nor green. In Experiment 2, we tested how mode switching affects larger parts of the color space. Thirteen participants donned and removed the glasses multiple times a day for 5 days, and we used a dissimilarity rating task to measure and track perception of many different colors. Across days, immediately upon donning the glasses, the world appeared less and less reddish (Experiment 1), and colors across the whole color space appeared more and more normal (Experiment 2). These results indicate that mode switching can be acquired from a once-daily experience, and it applies to most stimuli in a given environment. These findings may help to predict when and how mode switching occurs outside the laboratory.

Task-dependent contrast gain in anomalous trichromats.

Anomalous trichromacy is a form of color vision deficiency characterized by the presence of three cone types, but with shifted spectral sensitivities for L or M cones, causing a red-green color deficiency. However, long-term adaptation to this impoverished opponent input may allow for a more normal color experience at the suprathreshold level ("compensation"). Recent experimental evidence points to the presence of compensation in some tasks. The current study used threshold detection, suprathreshold contrast matching, and a reaction-time task to compare contrast coding in normal and anomalous observers along the cardinal cone-opponent axes. Compared to color normals, anomals required more L-M contrast, but not S contrast, to detect stimuli and to match an achromatic reference stimulus. Reaction times were measured for several contrast levels along the two cone-opponent axes. Anomals had higher overall reaction times, but their reaction-time versus contrast functions could be matched to those of controls simply by scaling contrast by the detection thresholds. Anomalous participants were impaired relative to controls for L-M stimuli in all three tasks. However, the contrast losses were three times greater for thresholds and reaction times than for suprathreshold matches. These data provide evidence for compensation in anomalous trichromats, but highlight the role that the experimental task plays in revealing it.

The McCollough World: Induction of orientation-contingent aftereffects with an altered-reality system.

The McCollough Effect is a color aftereffect produced by exposure to colored, oriented patterns. For example, following adaptation to vertical red and horizontal green stripes in alternation, vertical black and white patterns appear greenish, while horizontal black and white patterns appear reddish. The striking aspect of the McCollough Effect is that just a few minutes of adaptation can produce an aftereffect lasting days or weeks. Though this effect is easily induced, previous work has shown that stronger effects can be achieved with longer periods of adaptation. To allow especially long adaptation durations, the current work develops a novel method of induction of the McCollough Effect using live video feed, filtered by orientation, and viewed with a head-mounted display. Results showed that this "McCollough World" paradigm was as strong an inducer (per unit time) as traditional paradigms using gratings, while allowing observers to adapt comfortably for multiple hours. Two hours of McCollough World adaptation produced effects that were significantly larger than 20 min of traditional adaptation, which is close to the tolerance limits for gratings. This work provides insight into the features necessary for induction of the McCollough Effect and provides a strategy for creating especially strong and long-lasting color aftereffects.

Color Compensation in Anomalous Trichromats Assessed with fMRI.

Anomalous trichromacy is a common form of congenital color deficiency resulting from a genetic alteration in the photopigments of the eye's light receptors. The changes reduce sensitivity to reddish and greenish hues, yet previous work suggests that these observers may experience the world to be more colorful than their altered receptor sensitivities would predict, potentially indicating an amplification of post-receptoral signals. However, past evidence suggesting such a gain adjustment rests on subjective measures of color appearance or salience. We directly tested for neural amplification by using fMRI to measure cortical responses in color-anomalous and normal control observers. Color contrast response functions were measured in two experiments with different tasks to control for attentional factors. Both experiments showed a predictable reduction in chromatic responses for anomalous trichromats in primary visual cortex. However, in later areas V2v and V3v, chromatic responses in the two groups were indistinguishable. Our results provide direct evidence for neural plasticity that compensates for the deficiency in the initial receptor color signals and suggest that the site of this compensation is in early visual cortex.

Differences in the major fiber-tracts of people with congenital and acquired blindness.

In order to better understand how our visual system processes information, we must understand the underlying brain connectivity architecture, and how it can get reorganized under visual deprivation. The full extent to which visual development and visual loss affect connectivity is not well known. To investigate the effect of the onset of blindness on structural connectivity both at the whole-brain voxel-wise level and at the level of all major white-matter tracts, we applied two complementary Diffusion-Tension Imaging (DTI) methods, TBSS and AFQ. Diffusion-weighted brain images were collected from three groups of participants: congenitally blind (CB), acquired blind (AB), and fully sighted controls. The differences between these groups were evaluated on a voxel-wise scale with Tract-Based Spatial Statistics (TBSS) method, and on larger-scale with Automated Fiber Quantification (AFQ), a method that allows for between-group comparisons at the level of the major fiber tracts. TBSS revealed that both blind groups tended to have higher FA than sighted controls in the central structures of the brain. AFQ revealed that, where the three groups differed, congenitally blind participants tended to be more similar to sighted controls than to those participants who had acquired blindness later in life. These differences were specifically manifested in the left uncinated fasciculus, the right corticospinal fasciculus, and the left superior longitudinal fasciculus, areas broadly associated with a range of higher-level cognitive systems.

Visualizing Visual Adaptation.

Many techniques have been developed to visualize how an image would appear to an individual with a different visual sensitivity: e.g., because of optical or age differences, or a color deficiency or disease. This protocol describes a technique for incorporating sensory adaptation into the simulations. The protocol is illustrated with the example of color vision, but is generally applicable to any form of visual adaptation. The protocol uses a simple model of human color vision based on standard and plausible assumptions about the retinal and cortical mechanisms encoding color and how these adjust their sensitivity to both the average color and range of color in the prevailing stimulus. The gains of the mechanisms are adapted so that their mean response under one context is equated for a different context. The simulations help reveal the theoretical limits of adaptation and generate "adapted images" that are optimally matched to a specific environment or observer. They also provide a common metric for exploring the effects of adaptation within different observers or different environments. Characterizing visual perception and performance with these images provides a novel tool for studying the functions and consequences of long-term adaptation in vision or other sensory systems.

Adjusting to a sudden "aging" of the lens.

Color perception is known to remain largely stable across the lifespan despite the pronounced changes in sensitivity from factors such as the progressive brunescence of the lens. However, the mechanisms and timescales controlling these compensatory adjustments are still poorly understood. In a series of experiments, we tracked adaptation in observers after introducing a sudden change in lens density by having observers wear glasses with yellow filters that approximated the average spectral transmittance of a 70-year-old lens. Individuals were young adults and wore the glasses for 5 days for 8 h per day while engaged in their normal activities. Achromatic settings were measured on a CRT before and after each daily exposure with the lenses on and off, and were preceded by 5 min of dark adaptation to control for short-term chromatic adaptation. During each day, there was a large shift in the white settings consistent with a partial compensation for the added lens density. However, there was little to no evidence of an afterimage at the end of each daily session, and participants' perceptual nulls were roughly aligned with the nulls for short-term chromatic adaptation, suggesting a rapid renormalization when the lenses were removed. The long-term drift was also extinguished by brief exposure to a white adapting field. The results point to distinct timescales and potentially distinct mechanisms compensating for changes in the chromatic sensitivity of the observer.