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Thalamocortical dynamics of the McCollough effect: boundary-surface alignment through perceptual learning.

This article further develops the FACADE neural model of 3-D vision and figure-ground perception to quantitatively explain properties of the McCollough effect (ME). The model proposes that many ME data result from visual system mechanisms whose primary function is to adaptively align, through learning, boundary and surface representations that are positionally shifted due to the process of binocular fusion. For example, binocular boundary representations are shifted by binocular fusion relative to monocular surface representations, yet the boundaries must become positionally aligned with the surfaces to control binocular surface capture and filling-in. The model also includes perceptual reset mechanisms that use habituative transmitters in opponent processing circuits. Thus the model shows how ME data may arise from a combination of mechanisms that have a clear functional role in biological vision. Simulation results with a single set of parameters quantitatively fit data from 13 experiments that probe the nature of achromatic/chromatic and monocular/binocular interactions during induction of the ME. The model proposes how perceptual learning, opponent processing, and habituation at both monocular and binocular surface representations are involved, including early thalamocortical sites. In particular, it explains the anomalous ME utilizing these multiple processing sites. Alternative models of the ME are also summarized and compared with the present model.

Adaptation, Ocular↗

Common mechanisms for 2D tilt and 3D slant after-effects.

By presenting oriented Gabor patches either monocularly or binocularly, we dissociated retinal orientation from perceived tilt and perceived slant. After adapting to binocular patches, with zero apparent tilt and non-zero slant, small tilt after-effects (TAEs) and large slant after-effects (SAE) were measured. Adapting to monocular patches with non-zero tilt and zero slant produced large TAEs and smaller SAEs. This pattern of results suggests that a common, low-level adaptation to monocular orientation is involved in slant and tilt after-effects. However, the incomplete transfer between slant and tilt makes it clear that higher-level adaptation is also involved, perhaps at the level of surface representation.

Adaptation, Ocular↗

Paired and unpaired features can be equally effective in human depth perception.

The horizontal separation of the eyes results in the projection of slightly different images in each eye that are used to recover depth. One source of depth information is disparity, the relative position of paired features in the two eyes. Another source of depth information comes from features that are present in only one eye's view. These unpaired features arise from occlusion and by definition cannot generate a conventional disparity signal. Here we compare the depth signals generated by paired and unpaired features using stimuli that differ only in whether a given feature (a vertical gap) is paired or unpaired. Ecologically, both stimuli are consistent with two panels separated in depth at the gap, but only the paired gap provides a conventional disparity signal. We found strikingly that depth thresholds for the two gap conditions were the same and that there was perfect cross-adaptation of perceived depth from the unpaired to paired condition, strongly suggesting a common mechanism.

Contrast Sensitivity↗

Illusory jitter in a static stimulus surrounded by a synchronously flickering pattern.

The eyes are always moving even during fixation, making the retinal image move concomitantly. While these motions activate early visual stages, they are excluded from one's perception. A striking illusion reported here renders them visible: a static pattern surrounded by a synchronously flickering pattern appears to move coherently in random directions. There was a positive correlation between the illusion and fixational eye movements. A simulation revealed that motion computation artificially creates a motion difference between center and surround, which is usually a cue to object motion but now a wrong cue to seeing eye movements of oneself on-line. Therefore, this novel illusion indicates that the visual system normally counteracts shaky visual inputs due to small eye movements by using retinal, as opposed to extraretinal, motion signals. As long as they comprise common image motions over space, they are interpreted as coming from a static outer world viewed through moving eyes. Such visual stability fails in the condition of artificial flicker, because common image motions due to eye movements are registered differently between flickering and non-flickering regions.

Adult↗

Reversed-phi perception with motion-defined motion stimuli.

Perception of reversed-phi with motion-defined motion (MDM) stimuli was examined while varying various parameters including eccentricity. For peripheral viewing, reversed-phi was observed at all displacements between 30 degrees and 135 degrees. The perception most prominent at 90 degrees, but was disrupted by dichoptic presentation. These results suggest operations of an energy-based motion system similar to the first-order motion system for luminance motion, which most likely resides at a relatively early level (cf. [Vision Res. 33 (1993) 533]). For central viewing, reversed motion was observed only for larger displacements. The perceived motion at smaller displacements was predominantly in the forward direction. Transition between the two modes occurred around 90 degrees displacement. In addition, this motion perception was not disrupted by dichoptic presentation. This indicated the operation of a polarity independent matching-based motion system residing at a higher-level. Thus, the results indicate the involvement of at least two separate mechanisms for MDM detection, and that there is a dominance shift between the two systems according to the eccentricity.

Contrast Sensitivity↗

Perceptual filling-in: a parametric study.

We studied perceptual filling-in during maintained peripheral viewing of a uniform gray or red figure presented on a large textured background. Changes in the figure's size, shape, and eccentricity caused variations in the time required for filling-in that could be predicted from the size of its cortical projection within early visual areas. The data suggest that the time which elapsed before the figure was filled-in by its background reflects the time required for figure-ground segregation to fail, rather than a slow spread of the background across the figure. Our findings reveal interactions between surface segregation and filling-in which may be at the basis of normal surface perception.

Figural Aftereffect↗

Palinopsia.

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Cerebral Cortex↗

Facilitation from collinear flanks is cancelled by non-collinear flanks.

Detection of a central Gabor pattern is facilitated by the presence of collinear flanking patterns. We find that this facilitation is greatly reduced when the collinear flanks are combined with non-collinear flanks to form a coherent surround. These results are unlikely to be explained by mechanisms that merely transduce local contrast in a nonlinear fashion. A model wherein the outputs of such mechanisms are combined anisotropically provides a better account for these results.

Adaptation, Psychological↗

Perception and extrapolation of velocity and acceleration.

A moving target disappeared behind a screen and subjects predicted when the target passed behind a marker on the screen. When the target moved with constant velocity, predictions were extremely accurate, regardless of the spatial and temporal exposure and concealment of the target and regardless of its rate of velocity. When the target accelerated, accuracy of prediction decreased with increasing acceleration and with increasing target concealment. Analyses of the results suggest that the perception of velocity and acceleration is direct and accurate and that extrapolation of velocity and acceleration incorporates concrete and abstract characteristics of the motion that was seen. It is proposed that the motion perception system is tuned to accelerated rather than to constant velocity movement.

Acceleration↗

How much is an icon worth?

We report a new technique for assessing the amount of information extracted from the icon that follows a briefly presented picture. The problem of how to measure such information was formulated in terms of how much physical exposure of a picture an icon is worth. Consider two types of stimulus presentations, each with a base duration of d ms. The first is a d-ms picture followed by an icon, and the second is a d + a-ms picture not followed by an icon. How large does a have to be so that equivalent amounts of information are extracted in the two cases? To answer this question, we showed people pictures and later tested their memory for the pictures. We found that the physical exposure duration needed to reach a particular level of performance was approximately 100 ms longer when an icon was not permitted versus when the icon was permitted. This value was independent of the base duration and the luminance of the picture. Moreover, the same value was obtained using three different kinds of memory test and four different sets of pictures. We conclude that an icon is worth approximately 100 ms of additional physical exposure duration. A reasonable explanation for this robust equivalence between icon and stimulus is that the same encoding processes are responsible for extracting information from the icon and from the physical stimulus. Therefore, any variable that affects these encoding processes must affect extraction of information from the icon and the physical stimulus in an identical manner. This prediction was confirmed for one such variable, picture luminance.

Figural Aftereffect↗

Continuous measurement of visible persistence.

In the synchrony judgment paradigm, observers judge whether a click precedes or follows the onset of a light flash and, on other trials, whether or not a click precedes light termination. The interclick interval defines the duration of visible persistence. An elaboration of this method consists of two phases: In Phase 1, the luminance of a reference stimulus is psychophysically matched to the peak brightness of the test flash. Five luminance values between .1 and 1.0 of the reference stimulus are used subsequently. In Phase 2, a random one of the five reference stimuli, a test flash, and a click are presented; the observer judges whether the click occurred before or after the brightness of test flash reached the reference value (on onset trials) or decayed below it (on termination trials). This method was validated on 3 subjects with test stimuli whose luminance rises and decays slowly in time, and then was used to trace out the precise subjective rise and decay (temporal brightness response function) of brief flashes.

Acoustic Stimulation↗

The psychophysics of iconic storage.

Some simple models of iconic storage, based on the persisting responses of photoreceptors, were tested in two experiments. Substantial changes in such physical parameters as adapting luminance, stimulus luminance, and stimulus contrast produced little or no change in the duration of partial-report performance. This is at odds with most receptoral models. It seems unlikely that any model based on receptoral persistence can accommodate the results, thus forcing one to locate the icon beyond the receptors and probably beyond the retina as a whole.

Figural Aftereffect↗

Effects of spatial-frequency specific adaptation and target duration on visual persistence.

Two experiments investigated the properties of visual persistence as functions of spatial frequency, stimulus duration, and pattern-specific adaptation. In Experiment 1, increasing the duration of high spatial-frequency gratings from 50 to 500 msec decreased the duration of visual persistence produced by that grating to an asymptotic level. However, low-frequency gratings produced a constant estimate of visual persistence independent of presentation time. Also, spatial-frequency specific adaptation reduced the persistence of the high-frequency gratings to this asymptotic level, but the lower frequency persistence estimates already at this level were unaffected (Experiment 2). These findings are related to possible temporal properties of the sustained and transient visual systems.

Figural Aftereffect↗

Inverse-intensity effect in duration of visible persistence.

Duration of visible persistence can vary inversely with stimulus intensity. This inverse-intensity effect is obtained by varying the intensity of the stimuli or of the background, provided that the variations extend into the mesopic range. A similar relationship--known as the Ferry-Porter law--holds for the critical frequency at fusion (CFF). The authors propose that studies of CFF, 2-pulse threshold, and visible persistence can be encompassed within 1 conceptual framework in which the effect is modeled by the progressive reduction in the temporal extent of the positive phase of the system's response as the level of light adaptation changes from scotopic to photopic. In this context, the authors present an integrative scheme in which G. Sperling and M. M. Sondhi's (1968) formal model and M. Coltheart's (1980) neurophysiological conjecture are shown to be compatible and complementary accounts of the effect.

Attention↗

McCollough effects as conditioned responses: reply to Dodwell and Humphrey.

P. C. Dodwell and G. K. Humphrey (1990) criticized the Pavlovian conditioning analysis of the McCollough effect, claiming that it was conceptually flawed and that it did not assign the McCollough effect any useful function. In this article, it is suggested that the error-correction interpretation that Dodwell and Humphrey proposed as an ostensible alternative to the conditioning interpretation can be subsumed by the conditioning interpretation. Furthermore, the conditioning interpretation does ascribe a useful function to the McCollough effect.

Attention↗

On the relationship between stimulus intensity and duration of visible persistence.

Stimulus intensity and duration of visible persistence have been found to vary directly in some studies but inversely in others. Hawkins and Shulman (1979) have proposed that this inconsistency can be resolved by separating the studies that employed a decrement-threshold measure of persistence (Type I measure) from those that measured the total duration of persistence (Type II measure). They suggested that Type I measures yield an inverse relationship, whereas Type II measures yield a direct relationship between intensity and persistence. Hawkins and Shulman's model is incomplete in ways that are easily remedied. However, the model is totally contradicted by the experimental evidence. A new resolution of the inconsistent results is proposed in terms of retinal afterimages.

Attention↗

Suppression of visible persistence.

Five experiments were conducted to examine duration of visible persistence in sequences of stimuli. The basic display consisted of a point that stepped around a circular path on the face of an oscilloscope. Observers estimated the number of points seen simultaneously. Results were compared with a control condition in which the points were plotted in random order rather than sequentially. It was found that visible persistence of a point is suppressed if other points are shown nearby and after an appropriate delay. The degree of suppression depended on the spatial proximity of successive points. It was also found that both duration of visible persistence and degree of suppression increase with eccentricity in the visual field. The results are discussed in terms of two independent processes, persistence and suppression, that operate in a hierarchically antithetical relation.

Figural Aftereffect↗