Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “FIGURAL AFTEREFFECT”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 415 records · Page 23Linked to original sources
PubMed1986

Conjunction of color and form without attention: evidence from an orientation-contingent color aftereffect.

According to feature-integration theory (Treisman & Gelade, 1980), separable features such as color and shape exist in separate maps in preattentive vision and can be integrated only through the use of spatial attention. Many perceptual aftereffects, however, which are also assumed to reflect the features available in preattentive vision, are sensitive to conjunctions of features. One possible resolution of these views holds that adaptation to conjunctions depends on spatial attention. We tested this proposition by presenting observers with gratings varying in color and orientation. The resulting McCollough aftereffects were independent of whether the adaptation stimuli were presented inside or outside of the focus of spatial attention. Therefore, color and shape appear to be conjoined preattentively, when perceptual aftereffects are used as the measure. These same stimuli, however, appeared to be separable in two additional experiments that required observers to search for gratings of a specified color and orientation. These results show that different experimental procedures may be tapping into different stages of preattentive vision.

Adolescent↗
PubMed1983

On the relation of stereoacuity to interocular transfer of the motion and the tilt aftereffects.

Interocular transfer of both the motion and the tilt aftereffect were tested in 43 subjects with varying degrees of stereopsis, ranging from normal to stereoblind. Although there was an overall tendency for transfer to diminish with decreasing stereovision, stereoblind subjects always showed some transfer of the tilt aftereffect, and sometimes also of the motion aftereffect, while some subjects with normal stereothresholds had greatly reduced or no interocular transfer. No quantitative correlation between stereothresholds and amount of transfer could be found. The results indicate that there is no simple relationship between interocular transfer, stereopsis and cortical binocularity, as had been suggested previously.

Adaptation, Ocular↗
PubMed1993

Determinants of two-dimensional motion aftereffects induced by simultaneously- and alternately-presented plaid components.

Wenderoth, Bray and Johnstone [(1988) Perception, 17, 81-91] measured motion aftereffects induced on stationary vertical sine-wave gratings by horizontally drifting two-dimensional patterns (plaids). The adapting plaid component gratings were simultaneously or alternately presented and were oriented left and right of vertical by 15, 45 or 75 degrees. It was found that aftereffects decreased linearly in the alternating conditions as the plaid component orientations changed but this was not the case in the simultaneous adaptation conditions, a finding taken to be consistent with the hypothesis that one-dimensional aftereffects have a low level site (possibly V1) whereas two-dimensional effects have a higher level site (possibly MT). In three experiments, we have examined in more detail the determinants of aftereffects induced by simultaneous and alternating plaid components. The data suggest that the mechanisms involved are more complex than those put forward by Wenderoth et al. and that plaid perception utilizes both higher and lower level processes which can be referred to, respectively, as an intersection of constraints algorithm and a moving "blob" detector.

Adaptation, Ocular↗
PubMed2000

Color-specific depth mechanisms revealed by a color-contingent depth aftereffect.

Models of stereoscopic depth perception for both natural and random-dot images have focused mainly on the matching of achromatic features of binocular images. Recently, a growing body of research has investigated whether chromatic features can also contribute to the construction of stereoscopic depth. Here we present experiments yielding color-contingent depth aftereffects comparable in magnitude to those measured after adaptation to achromatic stimuli as evidence of neural mechanisms tuned to both color and depth. Furthermore, we report that the locus of the combined processing of color and depth is likely to lie beyond the site of binocular matching.

Adaptation, Physiological↗
PubMed1981

Peripheral movement, induced movement, and aftereffects from induced movement.

Substantial rotatory induced movement and aftereffects associated with induced movement were observed in a large statis patterned disc bounded at its periphery by a rotating patterned annulus. The area of the annulus was less than one tenth that of the disc, so its peripheral location seemed to be important in eliciting these phenomena. This was confirmed in two experiments comparing a peripheral annulus and a relatively central anulus in their ability to elicit induced movement and aftereffects in the same large static field. Aspects of the vection (induced self-movement) phenomenon may have been involved in generation of induced movement. This suggested that the motion-inducing properties of the peripheral annulus might have derived from: (i) its eccentric location in the perceiver's visual field; or (ii) its location with regard to the display itself. Two further experiments showed that (ii) was important for the elicitation of both induced movement and the aftereffects, and (i) was important for the elicitation of induced movement. Neurons responsive to relative movement in conjunction with lateral inhibition may provide a partial explanation for these effects. However, they do not explain why the visual system can assign considerable movement to a large static field under the conditions of these experiments.

Adult↗
PubMed1998

Aftereffect of high-speed motion.

A visual illusion known as the motion aftereffect is considered to be the perceptual manifestation of motion sensors that are recovering from adaptation. This aftereffect can be obtained for a specific range of adaptation speeds with its magnitude generally peaking for speeds around 3 deg s-1. The classic motion aftereffect is usually measured with a static test pattern. Here, we measured the magnitude of the motion aftereffect for a large range of velocities covering also higher speeds, using both static and dynamic test patterns. The results suggest that at least two (sub)populations of motion-sensitive neurons underlie these motion aftereffects. One population shows itself under static test conditions and is dominant for low adaptation speeds, and the other is prevalent under dynamic test conditions after adaptation to high speeds. The dynamic motion aftereffect can be perceived for adaptation speeds up to three times as fast as the static motion aftereffect. We tested predictions that follow from the hypothesised division in neuronal substrates. We found that for exactly the same adaptation conditions (oppositely directed transparent motion with different speeds), the aftereffect direction differs by 180 degrees depending on the test pattern. The motion aftereffect is opposite to the pattern moving at low speed when the test pattern is static, and opposite to the high-speed pattern for a dynamic test pattern. The determining factor is the combination of adaptation speed and type of test pattern.

Adaptation, Psychological↗
PubMed2005

The dynamics of visual adaptation to faces.

Several recent demonstrations using visual adaptation have revealed high-level aftereffects for complex patterns including faces. While traditional aftereffects involve perceptual distortion of simple attributes such as orientation or colour that are processed early in the visual cortical hierarchy, face adaptation affects perceived identity and expression, which are thought to be products of higher-order processing. And, unlike most simple aftereffects, those involving faces are robust to changes in scale, position and orientation between the adapting and test stimuli. These differences raise the question of how closely related face aftereffects are to traditional ones. Little is known about the build-up and decay of the face aftereffect, and the similarity of these dynamic processes to traditional aftereffects might provide insight into this relationship. We examined the effect of varying the duration of both the adapting and test stimuli on the magnitude of perceived distortions in face identity. We found that, just as with traditional aftereffects, the identity aftereffect grew logarithmically stronger as a function of adaptation time and exponentially weaker as a function of test duration. Even the subtle aspects of these dynamics, such as the power-law relationship between the adapting and test durations, closely resembled that of other aftereffects. These results were obtained with two different sets of face stimuli that differed greatly in their low-level properties. We postulate that the mechanisms governing these shared dynamics may be dissociable from the responses of feature-selective neurons in the early visual cortex.

Face↗
PubMed2000

Selective visual attention modulates the direct tilt aftereffect.

One's being able to allocate attention to particular regions or properties of the visual field is fundamental to visual information processing. Visual attention determines what input is carefully analyzed and what input is more or less ignored. But at what stage of the visual system is this process evident? We describe three experiments that demonstrate an effect of voluntary spatial attention and voluntary object-based attention on an orientation illusion (the tilt aftereffect) that is believed to take place in primary visual cortex. This finding, in which selective visual attention influences adaptation to visual orientation information, contributes to mounting evidence for a view of visual perception in which mutual interaction takes place between high-level and low-level subsystems.

Adult↗
PubMed2004

Stabilized structure from motion without disparity induces disparity adaptation.

3D structures can be perceived based on the patterns of 2D motion signals. With orthographic projection of a 3D stimulus onto a 2D plane, the kinetic information can give a vivid impression of depth, but the depth order is intrinsically ambiguous, resulting in bistable or even multistable interpretations. For example, an orthographic projection of dots on the surface of a rotating cylinder is perceived as a rotating cylinder with ambiguous direction of rotation. We show that the bistable rotation can be stabilized by adding information, not to the dots themselves, but to their spatial context. More interestingly, the stabilized bistable motion can generate consistent rotation aftereffects. The rotation aftereffect can only be observed when the adapting and test stimuli are presented at the same stereo depth and the same retinal location, and it is not due to attentional tracking. The observed rotation aftereffect is likely due to direction-contingent disparity adaptation, implying that stimuli with kinetic depth may have activated neurons sensitive to different disparities, even though the stimuli have zero relative disparity. Stereo depth and kinetic depth may be supported by a common neural mechanism at an early stage in the visual system.

Adaptation, Ocular↗
PubMed2006

Orientation dependence of the orientation-contingent face aftereffect.

Prolonged exposure to upright and inverted female and male faces produces opposite effects on subsequent judgments of the sex of faces depending on their orientation. We show that the magnitude of this orientation-contingent gender aftereffect can be predicted from simple aftereffects induced separately at the same orientations. The contingent aftereffect can also be induced in faces tilted 90 degrees to the right and left, eliminating any difference in face-processing strategy that may be in operation with upright and inverted faces. This suggests that neurons employing a single face encoding strategy can be activated in an orientation-specific manner.

Face↗
PubMed1991

Eye movements and the motion aftereffect: alternatives to the induced motion hypothesis.

It has been previously reported that prolonged unidirectional smooth pursuit often produces a negative motion aftereffect (MAE). This was believed to be caused by retinal image motion of stationary environmental contours during pursuit which subsequently produced a primary motion aftereffect in the tracking direction. The peripheral MAE then induced motion in the stationary tracking target resulting in illusory movement in the opposite direction. We have found that a negative MAE is also produced when the adapting field is devoid of any contours. Furthermore, the presence of a moving textured background in conjunction with smooth pursuit produced an MAE whose direction was inconsistent with the induced motion hypothesis. Since all examples of motion aftereffects in this study were associated with the pursuit aspect of the experiment rather than any interactions with background contours, it was proposed that the illusory motion had an oculomotor determinant. A scheme was tentatively outlined in which fixation suppression of an unregistered ocular drift following prolonged pursuit adaptation (pursuit after-nystagmus) produced the post-adaptive motion illusions.

Figural Aftereffect↗
PubMed2006

Strength of early visual adaptation depends on visual awareness.

We measured visual-adaptation strength under variations in visual awareness by manipulating phenomenal invisibility of adapting stimuli using binocular rivalry and visual crowding. Results showed that the threshold-elevation aftereffect and the translational motion aftereffect were reduced substantially during binocular rivalry and crowding. Importantly, aftereffect reduction was correlated with the proportion of time that the adapting stimulus was removed from visual awareness. These findings indicate that the neural events that underlie both rivalry and crowding are inaugurated at an early stage of visual processing, because both the threshold-elevation aftereffect and translational motion aftereffect arise, at least in part, from adaptation at the earliest stages of cortical processing. Also, our findings make it necessary to reinterpret previous studies whose results were construed as psychophysical evidence against the direct role of neurons in the primary visual cortex in visual awareness.

Adaptation, Ocular↗
PubMed1999

Is the size aftereffect direction selective?

We investigated whether the size aftereffect (apparent spatial-frequency shift after adaptation to slightly different frequencies) is direction selective; i.e., whether it is stronger for test stimuli moving in the adapting direction than the opposite direction. We used drifting sinusoidal gratings of various spatiotemporal frequencies for both adaptation and test stimuli, and the perceived test frequency was estimated by means of a matching technique with a staircase method. For the purpose of comparison, the post-adaptation threshold elevation was measured in addition to the size aftereffect. The results revealed that the direction of stimuli had no influence on the magnitude of the size aftereffect for a wide range of spatiotemporal frequencies, whereas the post-adaptation threshold elevation showed clear direction selectivity. Although there was a significant direction selectivity for the size aftereffect at low spatial and high temporal frequencies, the selectivity was much weaker than that seen in the threshold elevation data. These findings are discussed in relation to the validity of a unified account of selective adaptation at and above threshold contrast and the notion of the separate processing of pattern and motion information.

Adaptation, Psychological↗
PubMed1995

Adaptation to spatial offsets.

After prolonged viewing of a three-element target in which the middle element is spatially offset, subsequent viewing of the same three elements in alignment results in the middle element appearing to be offset in the opposite direction. This adaptational aftereffect to a spatial offset was investigated with elements which were spatial-frequency narrowband and equidetectable to ascertain (a) the properties of the mechanisms involved and (b) the nature of the underlying computation. Evidence is presented in favour of an orientational-grouping, rather than a purely positional computation, underlying this aftereffect. A dual site of adaptation is proposed: one which receives input from the orientation extracted from the output of linear filters, and another which receives input from the orientation derived from grouping processes working on the contrast-energy representation. These may correspond to the mechanisms which are thought to underlie the processing of real and subjective contours.

Adaptation, Ocular↗
PubMed1985

Spiral aftereffect in assessment of brain damage.

The potential role of the Archimedes spiral aftereffect, an illusory negative aftereffect of apparent movement, in the assessment of brain damage has been the subject of investigation by clinicians for over thirty years. The results bearing on its utility have been highly equivocal. This paper reviews the more important studies, identifies salient issues, and suggests directions for research into brain damage using this intriguing procedure.

Adolescent↗
PubMed2005

Depth aftereffects mediated by vertical disparities: evidence for vertical disparity driven calibration of extraretinal signals during stereopsis.

Perceptual adaptation often results in a repulsive aftereffect: stimuli are seen as biased away from the adaptation stimulus (). Here we report the absence of a repulsive aftereffect for a vertical gradient of vertical disparity (or vertical size ratio, VSR). We exposed observers to a binocular stimulus consisting of horizontal lines. This stimulus contains vertical, but not horizontal disparities. The visual system was able to measure the VSR of this stimulus: although the lines themselves always appeared unslanted, the VSR carried by the lines had a dramatic effect on the apparent slant of a horizontal row of dots, as predicted by recent accounts of Ogle's (1938) induced effect (e.g., Backus, Banks, van Ee, & Crowell, 1999). Yet we observed no repulsive aftereffect for the VSR signal: after adaptation to horizontal lines that were vertically larger in one eye, we found an attractive aftereffect, the magnitude of which was largest in stimuli that did not contain a VSR signal. We interpret these results as a case of recalibration: disagreement between extra-retinal eye position signals (EP) and VSR causes a recalibration in the use of EP as used in the stereoscopic perception of slant.

Adaptation, Physiological↗
PubMed1977

Recovery from adaptation to moving gratings.

Short-term adaptation to moving sinusoidal gratings results in a motion aftereffect which decays in time. The time decay of the motion aftereffect has been measured psychophysically, and it is found to depend on (i) the spontaneous recovery from the adapted state, and (ii) the contrast of the test grating. We have measured the decays for various test conditions. An extrapolation of the measurements allows us to obtain a decay which represents the time course of the spontaneous recovery of the direction-sensitive mechanisms.

Figural Aftereffect↗
PubMed1977

Distortions and disappearances of geometrical patterns.

Prolonged observation of a stationary grating has a number of perceptual consequences. Initially the lines appear well-resolved and straight. The lines then take on a wavy and oscillating appearance, which is followed by scintillation of the pattern. The scintillations are often accompanied by cloudy disappearances of the grating. A streaming or scintillating aftereffect is visible subsequently, upon viewing a homogeneous surface. The literature concerning these effects is reviewed and several experiments are reported which examined the apparent waviness and scintillating disappearances. The basis for the apparent waviness remains unresolved. It is suggested that the scintillations are produced by small involuntary eye movements over the contours and that the associated disappearances might be due to binocular rivalry.

Eye Movements↗