Effects of orientation-selective adaptation on the Z?llner illusion

The model of inhibitory interaction between orientation detectors was examined by prolonged presentation of grating patterns (which was expected to induce orientation-selective adaptation) before measurement of the Z?llner illusion. Adaptation effects were measured under conditions which excluded intrusion by the tilt aftereffect. In experiment 1, illusion magnitude greatly decreased only when the orientation of the adapting grating was the same as that of the inducing lines, which confirmed the first prediction deduced from the model. There was no effect of adapting grating when it was oriented more than 20 degrees away from the inducing lines. In experiment 2, adaptation effects were selective not only to orientation but also to spatial frequency. In experiment 3 it was shown that illusion reduction was mediated neither by lowered apparent contrast of the inducing lines nor by retinal adaptation. The results are discussed with respect to the nature of adaptation and possible physiological correlates.     

The effects of adaptation to square-wave gratings as a function of grating orientation

An adaptation technique was used to measure the selectivity or tuning for grating orientation in the visual system for different orientations of the inspection stimulus. Duration thresholds for grating patterns of constant luminance were determined for 13 test gratings oriented from ±5 to 90 deg away from each of five adaptation gratings: 0, 22, 45, 67, and 90 deg. Threshold data obtained for test gratings without prior adaptation indicated higher sensitivity for gratings oriented along the horizontal and vertical axis than along the oblique axis. After adaptation, thresholds increased (sensitivity was reduced) for gratings having similar orientations as the test gratings. However, the functions relating sensitivity reduction to degree of angular disparity between test and adaptation grating did not vary across the five inpsection orientations, i.e., selectivity or tuning for grating orientation appeared to be independent of the orientation of the adapting stimulus.     

Orientation-specific aftereffects and illusions in the perception of brightness

Orientation-specific brightness aftereffects were found when vertical and horizontal gratings of the same space-average luminance were viewed following alternate exposure to vertical and horizontal gratings that differed in space-average luminance. The vertical test grating appeared bright following exposure to a dim vertical grating, and dim after a bright vertical grating had been viewed. This aftereffect did not occur when the adaptation gratings had been seen by one eye and the test gratings by the other eye. An orientation-specific illusion in the perception of brightness was also found, with the white sectors of a vertical grating appearing brighter against a background of horizontal lines than they did against a background of vertical lines. Both distortions imply that there are detectors in the human visual system that are conjointly tuned to luminance and contour orientation.     

Laterality differences in sensitivity to line orientation as a function of adaptation duration

Since available evidence indicates that the two cerebral hemispheres are differentially sensitive to different types of stimulus information, and that they also utilize different strategies in processing information, is it possible that the two hemispheres are differentially sensitive to adaptation? Three groups of four subjects each were adapted to black and white gratings using three adapting durations: 500, 1,000, and 5,000 msec. Immediately following adaptation, a test grating was presented in either the left or right visual field. The task of the subject was to determine whether the lines of the adapting and test gratings had the same orientation or not. Analysis showed that in the 5,000-msec and 1,000-msec conditions, more errors occurred with left visual field presentations, responses to left visual field presentations took longer, and a bias-free measure showed that subjects were more sensitive to right visual field presentations. For the 500-msec group, there were no apparent differences between left and right visual fields presentations. The results indicate differential effects of adaptation on the two hemispheres, suggesting sensitivity differences between the two halves of the brain.     

Are curves detected by 'curvature detectors'?

Five experiments which attempted to evaluate the relationship between orientation and curvature selectivity in human vision are described. In the first two experiments, threshold elevation for curved gratings was measured after exposure to similar gratings, with the use of either an adaptation (experiment 1) or a masking (experiment 2) paradigm. In both experiments threshold elevation occurred which was selective for both the degree and the direction of curvature of the adapting pattern. Experiment 3 compared the effects of adapting to tilted rectilinear or vertical curved gratings upon threshold for a vertical rectilinear grating. Threshold elevation declined systematically as the adapting gratings were either tilted or made more curved. Experiment 4 measured curvature selectivity as a function of the orientation of a curved adapting grating. Threshold elevation declined as the adapting grating was tilted more, but curvature selectivity remained. Experiment 5 measured the orientation tuning for curved gratings directly. Threshold elevation declined to 50% of its maximum value at an adpating orientation of about 28 degrees. This was constant for all values of curvature used. The resulsts are discussed with reference to the question of whether the human visual system contains 'curvature detectors' or linear-contour detectors which respond to the tangents of curves.     

Orientation-selective adaptation during motion-induced blindness

When a global moving pattern is superimposed on high-contrast stationary or slowly moving stimuli, the latter occasionally disappear for periods of several seconds (motion-induced blindness, MIB). Here, an adaptation paradigm was used to determine if orientation-selective adaptation still occurs for the stimulus that is no longer visible. Two slowly drifting high-contrast Gabor patches were presented to observers. As soon as both patches disappeared, one was eliminated from the screen. After 2 s, two low-contrast Gabor patches were presented as tests at the same locations and observers were asked to report their orientations. The observers' performance was significantly higher when the orientation of the low-contrast test patch was orthogonal to the orientation of the high-contrast adapting patch (p < 0.0001) for the location where the patch was present during MIB, even though it was perceptually invisible. The observers' performance was not significantly different at the adjacent control location where the stimulus was absent during the MIB. Although no stimulus was visible at either location, orientation-selective adaptation was preserved only for the location at which the patch remained present. Since orientation information is processed in low-level visual areas such as the primary visual cortex (V1), we conclude that MIB originates in an area higher than V1.     

错觉轮廓的适应效应

错觉轮廓反映知觉的主动建构过程, 考察其是否存在适应效应有助于理解视觉系统反馈调节的特性。我们采用Kanizsa这种典型的错觉轮廓来研究其适应过程, 结果发现：Kanizsa错觉轮廓具有适应效应, 并且这种适应主要是由主观形成的整体轮廓造成的, 而不是由Pac-Man上的线条引起的。表明依赖于高级视觉皮层反馈调节的主观建构过程和自下而上的神经元信息一样, 会随呈现时间的增加, 神经活动减弱, 体现为适应效应。     

Development of illusory-contour perception in infants

We investigated whether infants from 8-22 weeks of age were sensitive to the illusory contour created by aligned line terminators. Previous reports of illusory-contour detection in infants under 4 months old could be due to infants' preference for the presence of terminators rather than their configuration. We generated preferential-looking stimuli containing sinusoidal lines whose oscillating, abutting terminators give a strong illusory contour in adult perception. Our experiments demonstrated a preference in infants 8 weeks old and above for an oscillating illusory contour compared with a stimulus containing equal terminator density and movement. Control experiments excluded local line density, or attention to alignment in general, as the basis for this result. In the youngest age group (8-10 weeks) stimulus velocity appears to be critical in determining the visibility of illusory contours, which is consistent with other data on motion processing at this age. We conclude that, by 2 months of age, the infant's visual system contains the nonlinear mechanisms necessary to extract an illusory contour from aligned terminators.     

Illusory form with inducers of opposite contrast polarity: Evidence for multistage integration

The perception of brightness differences in Ehrenstein figures and of illusory contours in phaseshifted line gratings was investigated as a function of the contrast polarity of the inducing elements. We presented either continuous lines or line-like arrangements composed of aligned dashes or dots whose spacing was varied. Ayes/no procedure was used in which naive observers had to decide whether or not they perceived a brightness difference in a given Ehrenstein figure or an illusory contour in a phase-shifted line grating. The results show that brightness differences are perceived to some extent in Ehrenstein figures with inducers of opposite polarity of contrast; however, the percentage ofyes responses was systematically lower and response times were longer than for figures with inducers of the same polarity. Phase-shifted line gratings with lines of opposite polarity of contrast yielded stronger illusory contours and shorter response times than those with lines of the same polarity. When the sign of contrast was not the same within a given line of induction, neither differences in brightness nor illusory contours were perceived. The results suggest that the mechanisms that lead to apparent differences in brightness are more sensitive to input of the same contrast polarity, the mechanisms generating illusory contours more sensitive to input of opposite polarity. The data are discussed in the light of a multistage approach to illusory form perception and some implications for cortical models of illusory contour integration are discussed.     

Evidence for a common motion mechanism of luminance-modulated and contrast-modulated patterns: selective adaptation.

Selective adaptation effects were measured with contrast-modulated patterns and sine-wave gratings in order to determine the extent to which the two patterns are processed by common mechanisms. Direction-specific adaptation effects were measured for a contrast-modulated adapting pattern and a test pattern. The contrast-modulated adapting pattern was composed of a sine-wave grating of 8 cycles deg-1 whose contrast was spatially modulated by a sinusoid of 1 cycle deg-1 at one of four levels: 100%, 60%, 30%, or 0%. The results showed that contrast-modulation thresholds for contrast-modulated gratings were raised by 0.3 to 0.5 log units following adaptation to a contrast-modulated grating moving in the same direction as the test pattern, relative to thresholds obtained following adaptation to a contrast-modulated grafting moving in the opposite direction. Cross-adaptation effects were also measured with a sine-wave adapting pattern and a contrast-modulated test pattern. The sine-wave adapting pattern was a sine-wave grating of 1 cycle deg-1 whose contrast was set to one of three levels: 16.4%, 1.25%, or 0%. The contrast-modulated test pattern was a sine-wave grating of 8 cycles deg-1 whose contrast was modulated by a sinusoid of 1 cycle deg-1. The results revealed that contrast-modulation thresholds for contrast-modulated gratings were raised by approximately 0.25 log units following adaptation to moving sine-wave gratings, relative to thresholds obtained following adaptation to a uniform field. Cross-adaptation effects were also obtained with a contrast-modulated adapting pattern and a sine-wave test pattern. The results support the view that signals generated from luminance-domain stimuli and from contrast-domain stimuli are processed by a common motion mechanism.     

Tracking without perceiving: a dissociation between eye movements and motion perception

Can people react to objects in their visual field that they do not consciously perceive? We investigated how visual perception and motor action respond to moving objects whose visibility is reduced, and we found a dissociation between motion processing for perception and for action. We compared motion perception and eye movements evoked by two orthogonally drifting gratings, each presented separately to a different eye. The strength of each monocular grating was manipulated by inducing adaptation to one grating prior to the presentation of both gratings. Reflexive eye movements tracked the vector average of both gratings (pattern motion) even though perceptual responses followed one motion direction exclusively (component motion). Observers almost never perceived pattern motion. This dissociation implies the existence of visual-motion signals that guide eye movements in the absence of a corresponding conscious percept.     

Adaptation to spiral motion in crowding condition

When a single, moving stimulus is presented in the peripheral visual field, its direction of motion can be easily distinguished, but when the same stimulus is flanked by other similar moving stimuli, observers are unable to report its direction of motion. In this condition, known as 'crowding', specific features of visual stimuli do not access conscious perception. The aim of this study was to investigate whether adaptation to spiral motion is preserved in crowding conditions. Logarithmic spirals were used as adapting stimuli. A rotating spiral stimulus (target spiral) was presented, flanked by spirals of the same type, and observers were adapted to its motion. The observers' task was to report the rotational direction of a directionally ambiguous motion (test stimulus) presented afterwards. The directionally ambiguous motion consisted of a pair of spirals flickering in counterphase, which were mirror images of the target spiral. Although observers were not aware of the rotational direction of the target and identified it at chance levels, the direction of rotation reported by the observers during the test phase (motion aftereffect) was contrarotational to the direction of the adapting spiral. Since all contours of the adapting and test stimuli were 90 degrees apart, local motion detectors tuned to the directions of the mirror-image spiral should fail to respond, and therefore not adapt to the adapting spiral. Thus, any motion aftereffect observed should be attributed to adaptation of global motion detectors (ie rotation detectors). Hence, activation of rotation-selective cells is not necessarily correlated with conscious perception.     

Inhibition between channels selective to contour orientation and wavelength in the human visual system

Recent studies have demonstrated inhibition between channels selective to contour orientation in the human visual system. On the basis of adaptation studies, it has also been suggested that the human visual system contains channels jointly responsive to both contour orientation and wavelength. The present paper investigates inhibition between such channels. Two experiments demonstrated that, with simultaneous presentation of a center vertical target grating and a concentric surround grating, the threshold and the apparent orientation of the center grating depended on the relative orientations of the two gratings and also on whether they were viewed in the same or in different colored light. Color selectivity in both experiments was found across a wider range of angular separations than has generally been reported for successive presentation of the two stimuli. These results suggest inhibition between channels selective to combinations of contour orientation and wavelength in the human visual system.     

The nature of learned categorical perception effects: a psychophysical approach

Categorical perception is often cited as a striking example of cognitive influences on perception. However, some evidence suggests the term is a misnomer, with effects based on cognitive not perceptual processing. Here, using a psychophysical approach, we provide evidence consistent with a learned categorical perception effect that is dependent on analysis within the visual processing stream. An improvement in participants' discrimination between grating patterns that they had learned to place in different categories was 'tuned' around the orientation of the patterns experienced during category learning. Thus, here, categorical perception may result from attentionally modulated perceptual learning about diagnostic category features, based upon orientation-selective stages of analysis. This argues strongly that category learning can alter our perception of the world.     

Orientation-specific aftereffects to mentally generated lines

After staring at a pattern of tilted lines, subsequent lines appear to be tilted in the opposite direction (direct tilt aftereffect, TAE). In a previous fMRI study we have demonstrated a direct TAE solely induced by the mental imagination accompanied by adaptation of orientation-selective neurons located in the extrastriate cortex, supporting the assumption of a perception-like coding of mental images. In this study we enlarge and specify the evidence for a perception-like coding of orientation-imagination. First, we replicated the previously detected direct TAE induced by line imagination with altered design-variations to control possible perceptual task confounds. Second, we tried to induce two other orientation-specific aftereffects: indirect TAE and contrast-threshold elevation aftereffect by mental imagery. The results replicate a robust direct TAE by mental imagery and by visual stimulation, with no influence of attentional resource allocation or perceptual task confounds. We could not induce an indirect TAE, but observed a perception bias in the opposite direction of the indirect TAE. The mental imagery of lines induced no orientation-selective contrast-threshold elevation aftereffect. In general, mental imagery seems to influence visual perception, indicating that perceptual resources are used by mental imagery. However, the utilisation of visual resources seems to be somewhat different from utilisation by perception.     

Stabilized images: Functional relationships among populations of orientation-specific mechanisms in the human visual system

Two experiments are presented in which fading rates of stabilized line stimuli were measured following prolonged adaptation to nonstabilized grating patterns in various orientations. Results indicated that some orientation-specific effects are sensitive to small variations of orientation around an optimal orientation, as well as to stimuli rotated 90 deg from the optimal orientation. These data were interpreted in terms of interactions among populations of orientation-specific mechanisms in the human visual system.     

Optic-flow-based perception of two-dimensional trajectories and the effects of a single landmark

Human observers can detect their heading direction on a short time scale on the basis of optic flow. We investigated the visual perception and reconstruction of visually travelled two-dimensional (2-D) trajectories from optic flow, with and without a landmark. As in our previous study, seated, stationary subjects wore a head-mounted display in which optic-flow stimuli were shown that simulated various manoeuvres: linear or curvilinear 2-D trajectories over a horizontal plane, with observer orientation either fixed in space, fixed relative to the path, or changing relative to both. Afterwards, they reproduced the perceived manoeuvre with a model vehicle, whose position and orientation were recorded. Previous results had suggested that our stimuli can induce illusory percepts when translation and yaw are unyoked. We tested that hypothesis and investigated how perception of the travelled trajectory depends on the amount of yaw and the average path-relative orientation. Using a structured visual environment instead of only dots, or making available additional extra-retinal information, can improve perception of ambiguous optic-flow stimuli. We investigated the amount of necessary structuring, specifically the effect of additional visual and/or extra-retinal information provided by a single landmark in conditions where illusory percepts occur. While yaw was perceived correctly, the travelled path was less accurately perceived, but still adequately when the simulated orientation was fixed in space or relative to the trajectory. When the amount of yaw was not equal to the rotation of the path, or in the opposite direction, subjects still perceived orientation as fixed relative to the trajectory. This caused trajectory misperception because yaw was wrongly attributed to a rotation of the path: path perception is governed by the amount of yaw in the manoeuvre. Trajectory misperception also occurs when orientation is fixed relative to a curvilinear path, but not tangential to it. A single landmark could improve perception. Our results confirm and extend previous findings that, for unambiguous perception of ego-motion from optic flow, additional information is required in many cases, which can take the form of fairly minimal, visual information.     

Color-luminance relationships and the McCollough effect

The McCollough effect is an orientation-specific color aftereffect induced by adapting to colored gratings. We examined how the McCollough effect depends on the relationships between color and luminance within the inducing and test gratings and compared the aftereffects to the color changes predicted from selective adaptation to different color-luminance combinations. Our results suggest that the important contingency underlying the McCollough effect is between orientation and color-luminance direction and are consistent with sensitivity changes within mechanisms tuned to specific color-luminance directions. Aftereffects are similar in magnitude for adapting color pairs that differ only in S cone excitation or L and M cone excitation, and they have a similar dependence on spatial frequency. In particular, orientation-specific aftereffects are induced for S cone colors even when the grating frequencies are above the S cone resolution limit. Thus, the McCollough effect persists even when different cone classes encode the orientation and color of the gratings.     

社会拥挤对金钱捐赠意愿的影响：自我表达需要的中介作用

通过四个实验（474名被试）,采用三种不同的刺激物操纵拥挤感,在三种不同情境下测量两类金钱捐赠行为,来探索拥挤感对金钱捐赠的影响。结果发现：拥挤感强（vs. 弱）的被试有更高的金钱捐赠意愿、更高的月度和年度捐赠金额;其中个体的自我表达需要发挥中介作用,即体验到强拥挤感的个体的自我表达需要更强,为了满足这一需要,更积极响应金钱捐赠的呼吁。     

Color—luminance relationships and the McCollough effect

The McCollough effect is an orientation-specific color aftereffect induced by adapting to colored gratings. We examined how the McCollough effect depends on the relationships between color and luminance within the inducing and test gratings and compared the aftereffects to the color changes predicted from selective adaptation to different color—luminance combinations. Our results suggest that the important contingency underlying the McCollough effect is between orientation and color—luminance direction and are consistent with sensitivity changes within mechanisms tuned to specific color—luminance directions. Aftereffects are similar in magnitude for adapting color pairs that differ only in S cone excitation or L and M cone excitation, and they have a similar dependence on spatial frequency. In particular, orientation-specific aftereffects are induced for S cone colors even when the grating frequencies are above the S cone resolution limit. Thus, the McCollough effect persists even when different cone classes encode the orientation and color of the gratings.