Differences in color fading and recovery under sustained fixation.

More than two centuries ago, Swiss philosopher I. P. V. Troxler announced in 1804 that fixated images fade away during normal vision. Since this declaration, the phenomenon now known as Troxler fading has become the subject of intensive research. Many researchers were eager to find out why we experience image fading and under what conditions image restoration happens. Here, we investigated the dynamics of color stimulus fading and recovery under sustained eye fixation. The objective of the experiments was to find out which colors fade and recover faster under isoluminant conditions. The stimuli were eight blurred color rings extending to 13° in size. Four unique colors (red, yellow, green, and blue) and four intermediate colors (magenta, cyan, yellow-green, and orange) were used. Stimuli were displayed on a computer monitor with a gray background and were isoluminant to the background. The presentation of the stimulus lasted 2 min and subjects were required to look at the fixation point in the middle of the ring and suppress eye movements. The task for subjects was to report the moments of change in the stimulus visibility by four stages of stimulus completeness. We found that all investigated colors undergo fading and recovery cycles during 2 min of observation. The data suggest that magenta and cyan colors have faster stimulus fading and undergo more recovery cycles, while longer wavelength colors slow down stimulus fading.

Neural Model of Coding Stimulus Orientation and Adaptation.

The coding of line orientation in the visual system has been investigated extensively. During the prolonged viewing of a stimulus, the perceived orientation continuously changes (normalization effect). Also, the orientation of the adapting stimulus and the background stimuli influence the perceived orientation of the subsequently displayed stimulus: tilt after-effect (TAE) or tilt illusion (TI). The neural mechanisms of these effects are not fully understood. The proposed model includes many local analyzers, each consisting of two sets of neurons. The first set has two independent cardinal detectors (CDs), whose responses depend on stimulus orientation. The second set has many orientation detectors (OD) tuned to different orientations of the stimulus. The ODs sum up the responses of the two CDs with respective weightings and output a preferred orientation depending on the ratio of CD responses. It is suggested that during prolonged viewing, the responses of the CDs decrease: the greater the excitation of the detector, the more rapid the decrease in its response. Thereby, the ratio of CD responses changes during the adaptation, causing the normalization effect and the TAE. The CDs of the different local analyzers laterally inhibit each other and cause the TI. We show that the properties of this model are consistent with both psychophysical and neurophysiological findings related to the properties of orientation perception, and we investigate how these mechanisms can affect the orientation's sensitivity.

Fast cyclic stimulus flashing modulates perception of bi-stable figure.

Many experiments have demonstrated that the rhythms in the brain influence the initial perceptual information processing. We investigated whether the alternation rate of the perception of a Necker cube depends on the frequency and duration of a flashing Necker cube. We hypothesize that synchronization between the external rhythm of a flashing stimulus and the internal rhythm of neuronal processing should change the alternation rate of a Necker cube. Knowing how a flickering stimulus with a given frequency and duration affects the alternation rate of bistable perception, we could estimate the frequency of the internal neuronal processing. Our results show that the perception time of the dominant stimulus depends on the frequency or duration of the flashing stimuli. The duration of the stimuli, at which the duration of the perceived image was maximal, was repeated periodically at 4 ms intervals. We suppose that such results could be explained by the existence of an internal rhythm of 125 cycles/s for bistable visual perception. We can also suppose that it is not the stimulus duration but the precise timing of the moments of switching on of external stimuli to match the internal stimuli which explains our experimental results. Similarity between the effects of flashing frequency on alternation rate of stimuli perception in present and previously performed experiment on binocular rivalry support the existence of a common mechanism for binocular rivalry and monocular perception of ambiguous figures.

Influences of prolonged viewing of tilted lines on perceived line orientation: the normalization and tilt after-effect.

Gibson [J. Exp. Psychol. 16, 1 (1993)] observed that during prolonged viewing, a line perceptually rotates toward the nearest vertical or horizontal meridian (the normalization effect), and moreover, the perceived orientation of a subsequently presented line depends on the orientation of the adapting one (the tilt after-effect). The mechanisms of both phenomena remain poorly understood. According to our experimental results, the adapting line perceptually rotates to the nearest of three orientations: vertical, horizontal, and diagonal. We propose a simple neuronal model of orientation detectors whose responses are determined by the cardinal detectors. It is shown that both normalization and tilt after-effect may be explained by adaptation of these cardinal detectors.