Effects of spatial filtering and lack of effects of visual imagery on pattern-contingent color aftereffects

Checkerboards contain fundamental two-dimensional Fourier components oriented 45° from the edges of individual checks. Previous studies have shown that contingent color aftereffects following adaptation to chromatic checkerboard stimuli were associated with the fundamental components rather than the edges, In the present experiments, we measured contingent color aftereffects, using the method of constant stimuli, after subjects adapted to unfiltered checkerboards and checkerboards with the fundamental Fourier components removed. The adaptation stimuli were magenta (or green) squares and green (or magenta) diamonds; the test stimuli were vertical or oblique sine-wave gratings with different saturations, After adaptation to unfiltered checkerboards, aftereffects contingent on the fundamental components were obtained. In contrast, after adaptation to filtered stimuli, aftereffects of smaller magnitude were found to be aligned with the edges. The data support the previous findings of spatial-frequency-contingent color after-effects with checkerboard adaptation stimuli and indicate that the aftereffects can be associated with edges if the fundamental components of adaptation stimuli are removed by spatial filtering. We reexamined the possibility of color aftereffects induced by imagery of checkerboards. Contrary to the previous reports, no significant aftereffects were obtained.     

The functional equivalence of mental images and errors of movement.

Four experiments are reported demonstrating that mental images are functionally equivalent to physical errors of movement in producing changes in visual-motor coordination, at both central and peripheral levels of the visual-motor system. In the first experiment, subjects in one condition pointed at a target seen through laterally displacing prisms and were instructed to imagine pointing errors identical to those recorded previously for subjects in a separate condition who actually observed their pointing errors. Changes in pointing accuracy during adaptation procedures and visual-motor aftereffects following these procedures for subjects who imagined their errors were proportional to visual-motor shifts and aftereffects for subjects who observed their errors. In the second experiment, these same imagery instructions resulted in identical pointing shifts and aftereffects even in the case where prisms did not displace the target. The third experiment showed that when subjects believe that their mental images of pointing errors do not correspond to their actual pointing errors, pointing aftereffects result that are characteristic of the processing of error information at peripheral, but not central, levels of the visual motor system. The final experiment showed that when subjects do believe that their images of pointing errors correspond to actual pointing errors, but imagine the pointing movement itself in addition to their errors, pointing aftereffects result that are characteristic of the processing of error information at central, but not peripheral, levels of the visual-motor system. Contributions to visual-motor aftereffects from these two levels appear to be additive. Another significant result was that, in the imagery feedback conditions of each experiment, subjects who gave high ratings of vividness to their mental imagery showed the greatest magnitude of pointing aftereffects. These findings establish that mental images for errors of movement can produce stable visual-motor changes that cannot be accounted for simply by subjects' expectations regarding the actual consequences of their actions.     

Further studies of the McCollough effect

Following prolonged viewing of black and white striped pattems in colored light, red and green aftereffects that lasted as long as 3 days were seen on the patterns, illuminated with white light. Altemate exposures of a vertical pattern of stripes in green light and a horizontal in white light (or a vertical in white light and a horizontal in red light) produced a red aftereffect on the vertical pattern and a green on the horizontal. The red and green aftereffects were also produced with a single vertical pattern. Adaptation colors that were at all greenish produced a red aftereffect on a vertical pattern and a green on a horizontal, whereas colors that were at all reddish produced a green aftereffect on a vertical pattern and a red on a horizontal. Colors near pure blue and pure yellow, which had little red or green content, produced weak aftereffects. The saturation of the aftereffects on the vertical grating varied in proportion to the red or green content of the adaptation color. Vivid red and green aftereffects were frequently obtained with the vertical and horizontal adaptation patterns paired with colors that closely bracketed pure yellow or pure blue. In all cases, the aftereffects gradually desaturated as the head was gradually tilted down to the side; the colors on each test pattern, vertical and horizontal, vanished at 45-deghead tilt and reversed beyond 45 deg.     

Contingent aftereffects: lateral interactions between color and motion

A randomly dotted yellow disk was rotated at a speed of 5 rpm, alternating in direction every 10 sec. Its change in direction of rotation was paired with a change in surround color, which was either red or green. After 15 min of exposure, observers reported vivid motion aftereffects contingent on the color of both the stationary disk and the surround, even though during adaptation only motion or color was associated with either alone. In further experiments, it was established that a change in color (or direction of motion) of the disk could be associated with a change in direction of motion (or color) of the surround. Such lateral effects were found even when a wide (5 degree) annulus was introduced between the disk and the surround during adaptation and testing. Furthermore, the aftereffects generalized to the annulus, which was not associated with either color or motion during adaptation. However, when the disk alone was adapted to color and motion, no generalization to the surround was found (and vice versa), suggesting that the effects are not produced by adaptation of large receptive fields or by scatter of light within the eye. The results appear to conflict with the ideas that contingent aftereffects are confined to the adapted area of the retina and that they are built up by links between single-duty neurones, and with an extreme view of the segregation of color and motion early in human vision.     

Prism adaptation in left-handers

Two experiments with left-handers examined the features of prism adaptation established by previous research with right-handers. Regardless of handedness, (1) rapid adaptation occurs in exposure pointing with developing error in the opposite direction after target achievement, especially with early visual feedback in target pointing; (2) proprioceptive or visual aftereffects are larger, depending on whether visual feedback is available early or late, respectively, in target pointing; (3) the sum of these aftereffects is equal to the total aftereffect for the eye-hand coordination loop; (4) intermanual transfer of visual aftereffects occurs only for the dominant hand; and (5) visual aftereffects are larger in left space when the dominant hand is exposed to leftward displacement. A notable handedness difference is that, while transfer of proprioceptive aftereffects only occurs to the nondominant hand in right-handers, transfer occurs in both directions for left-handers, but regardless of handedness, such transfer only occurs when the exposed hand is tested first after exposure. A discussion then focuses on the implications of these data for a theory of handedness.     

The quantitative measure of pattern representation in images using orientation-specific color aftereffects

A quantitative method is developed for assessing the quality of pattern information in imagery, using the magnitude of color aftereffects as an objective index. Subjects were given instructions to project imagined bar patterns of particular width and orientation onto adapting color fields, in such a manner as to simulate standard conditions for establishing the McCollough effect. Our control procedures indicate that the resulting orientation-specific complementary color aftereffects cannot be attributed to the conditioning of particular directions of eye scanning movements to color processing during adaptation, or to other possible sources of experimental bias. Furthermore, subjects who rated themselves prior to the adaptation procedure as having relatively vivid imagery showed significantly larger aftereffects than those who reported having relatively low imagery. These results not only provide an important confirmation of our earlier finding that imagination can replace physical pattern information in the formation of basic color-feature associations in the human visual system, but also demonstrate that these aftereffects can provide a practical measure of the fidelity of pattern representation in visual images.     

Spatial frequency content of visual imagery

Three experiments employing the McCollough paradigm were conducted to determine the spatial-frequency content of visual imagery. In Experiment 1, large and reliable pattern-contingent color aftereffects were obtained after adaptation to visual imagery. The direction of the aftereffects indicated that subjects were adapting to higher spatial frequencies in their imagery. These results contrast with the data of Experiment 2, which demonstrate that color aftereffects obtained with adaptation to physically present stimuli are mediated by the fundamental spatial frequency components. The magnitude of the imagery-induced aftereffects in Experiment 1 equaled the magnitude of the externally induced aftereffects obtained in Experiment 2 with the same subjects. By blurring the to-be-imaged patterns (Experiment 3), the fundamental Fourier components became the salient perceptual features of the stimuli, and the direction of the imagery-induced aftereffects was reversed from that of Experiment 1, indicating that the spatial frequency content of the imagery had changed from higher to lower frequencies. Under normal viewing conditions, subjects use the higher spatial frequencies associated with the perceptually salient edges of stimuli to construct their images. The results of Experiments 1 and 3 are discussed in light of a current controversy over the nature of information representation in imagery, and it is concluded that support has been obtained for the analog model of visual imagery.     

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.     

Stimulus selectivity of figural aftereffects for faces

Viewing a distorted face induces large aftereffects in the appearance of an undistorted face. The authors examined the processes underlying this adaptation by comparing how selective the aftereffects are for different dimensions of the images including size, spatial frequency content, contrast, and color. Face aftereffects had weaker selectivity for changes in the size, contrast, or color of the images and stronger selectivity for changes in contrast polarity or spatial frequency. This pattern could arise if the adaptation is contingent on the perceived similarity of the stimuli as faces. Consistent with this, changing contrast polarity or spatial frequency had larger effects on the perceived identity of a face, and aftereffects were also selective for different individual faces. These results suggest that part of the sensitivity changes underlying the adaptation may arise at visual levels closely associated with the representation of faces.     

Overshadowing and blocking of the orientation-contingent color aftereffect: Evidence for a conditioning mechanism

Orientation-contingent color aftereffects have been interpreted by nonassociative mechanisms (adaptation of neural units that are both color and orientation specific) and by associative mechanisms (conditioning resulting from the pairing of pattern and hue). To evaluate associative accounts, contingent aftereffects were induced by exposing subjects to compound chromatic grid patterns consisting of two component gratings: one was horizontal or vertical, and the other a left- or right-learning diagonal. The ability of a component grating to elicit a color aftereffect depended on the relative salience and the aftereffect training history of the grating components. That is, orientation-contingent color aftereffects, like other conditional responses, display overshadowing and blocking. The results suggest that conditioning contributes to these aftereffects.     

Generalization of prism adaptation

Prism exposure produces 2 kinds of adaptive response. Recalibration is ordinary strategic remapping of spatially coded movement commands to rapidly reduce performance error. Realignment is the extraordinary process of transforming spatial maps to bring the origins of coordinate systems into correspondence. Realignment occurs when spatial discordance signals noncorrespondence between spatial maps. In Experiment 1, generalization of recalibration aftereffects from prism exposure to postexposure depended upon the similarity of target pointing limb postures. Realignment aftereffects generalized to the spatial maps involved in exposure. In Experiment 2, the 2 kinds of aftereffects were measured for 3 test positions, one of which was the exposure training position. Recalibration aftereffects generalized nonlinearly, while realignment aftereffects generalized linearly, replicating Bedford (1989, 1993a) using a more familiar prism adaptation paradigm. Recalibration and realignment require methods for distinguishing their relative contribution to prism adaptation.     

Arm-body adaptation with passive arm movements

Two experiments investigated the aftereffects of pointing with passive movements during exposure to 15-deg laterally displacing wedge pnsms. Experiment 1 compared exposure with passive and active supported movements when the aftereffects were measured with the arm still in the passive movement device. Following passive exposure and active supported exposure, 5.6 and 7.9 deg, respectively, of arm-body adaptation were measured. In Experiment 2, the passive and active supported exposure tasks were compared with a third task in which similar movements were made with the arm fully supported by the muscles. Aftereffects were measured with active test movements. The amount of arm-body adaptation measured following passive exposure was decreased to 2.8 deg, and following active supported exposure it was decreased to 2.8 deg, while following exposure with normal active movements, 5.3 deg of arm-body adaptation was found. The results suggest that when the arm remains outstretched during prism exposure, adaptation is specific to this extended posture.     

Does action make the link between number and space representation? Visuo-manual adaptation improves number bisection in unilateral neglect

If the visual world is artificially shifted by only 10 degrees, people initially experience difficulty in directing their actions toward visual goals, but then rapidly compensate the visual distortion. The consequence of such adaptation can be measured as visual and proprioceptive aftereffects, as well as by performance on pointing tasks without visual feedback. Recent work has shown that more cognitive deficits can be improved following prism adaptation in patients with unilateral neglect. Here we show that a short visuo-manual adaptation to prisms improves performance on a mental number-bisection task recently shown to be impaired in unilateral neglect. The association previously found between space and number representation (the mental number line) may thus be grounded in common action principles. Our results suggest that visuo-motor plasticity functionally links parietal areas involved in space and number representation.     

Dichoptic induction of movement aftereffects contingent on color and on orientation

Some comparative experiments on the dichoptic induction of the movement aftereffect (MAE) contingent on color and the MAE contingent on orientation are reported. Colorcontingent movement aftereffects could be evoked only when the eye which had viewed color during adaptation also viewed color during test sessions. When the apparent color of the test field was changed by binocular color rivalry, contingent movement aftereffects (CMAEs) appropriate to the suppressed color were reported. After dichoptic induction of the orientation-contingent MAE, aftereffects could be obtained whether the eliciting gratings and stationary test fields were presented together to either eye alone or were dichoptically viewed.     

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.     

Conditioned adaptation to prismatic displacement

Adaptation to prismatic displacement was conditioned to the wearing of a pair of goggles in 240 min of training by employing Taylor’s alternation training technique. The alternation was between training exposures with both the prism and the goggles presented to S and with both absent. After the training, both the pointing to a visual target test and the pointing straight ahead test measured more adaptation and more aftereffects of adaptation when the goggles were     

Absence of binocular interaction between spatial and color attributes of visual stimuli

The hypothesis that induction of the McCollough effect (spatially selective color aftereffects) entails adaptation of monocularly driven detectors tuned to both spatial and color attributes of the visual stimulus was examined in four experiments. The McCollough effect could not be generated by displaying contour information to one eye and color information to the other eye during inspection, even in the absence of binocular rivalry. Nor was it possible to induce depth-specific color aftereffects following an inspection period during which random-dot stereograms were viewed, with crossed and uncrossed disparity seen in different colored light. Masking and aftereffect in the perception of stereoscopic depth were also nonselective to color; in both cases, perceptual distortion was controlled by stereospatial variables but not by the color relationship between the inspection and test stimuli. The results suggest that binocularly driven spatial detectors in human vision are insensitive to wavelength.     

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.     

数量适应后效的皮层映射特征

本研究探讨了观察者与观察目标存在相对运动时视觉系统对目标数量特征的适应后效的皮层映射特征, 并与对比度适应后效的映射规律进行比较。包括两项实验。其中, 实验一要求被试在适应目标后转换注视点, 考察眼跳后相同和不同视网膜区域以及相同和不同空间区域的适应后效, 发现数量适应后效具有部分空间-皮层映射特性, 而对比度适应后效则表现出完全的视网膜-皮层映射特征。实验二采用固定的注视点, 考察目标运动后目标原位置和新位置区域的适应后效, 发现数量适应后效不完全依赖于视网膜-皮层映射, 它可以“追随”客体运动重新映射到新的位置, 表现出基于客体映射的特征, 而对比度适应后效则完全依赖于视网膜-皮层映射, 不能“追随”客体移动在目标新位置重新形成映射。两项实验结果提示, 相对于对比度等低级表面特征而言, 数量特征对目标的描述涉及更高的加工水平, 它可以与观察目标的相对运动信息进行整合, 且这种整合在眼跳和非眼跳的观察条件下都可发生。