Recovery from adaptation as a function of stimulus orientation

These experiments examined the oblique effect in an adaptation paradigm. Reaction times (RT) to the presence of a grating test stimulus were obtained following adaptation to either a blank field or a grating of the same orientation as the test stimulus. Horizontal, vertical, and oblique test and adaptation orientations were employed. Test gratings were presented at several interstimulus intervals following offset of the adaptation stimulus. RTs following grating adaptation were elevated to a greater extent (relative to blank adaptation) for oblique then for horizontal or vertical stimuli, for two grating spatial frequencies. Differences in RT can be related to differences in sensitivity among channels responsible for detection of the various orientations.

     

Orientation and spatial frequency effects on linear afterimages: The retinal reference for selectivity — A supplementary report

Afterimages of gratings oriented vertically or at 45 deg relative to gravity were generated with the head upright or tilted so that the retinal meridian was inclined 45 deg. The duration of visibility of the whole afterimage was longer for the vertical grating when the head was upright and for the 45-deg grating when the head was tilted. It was concluded that this orientation selectivity of afterimages is dependent upon the orientation of the grating with respect to the retinal meridian rather than to the direction of gravity.     

Variations in apparent spatial frequency with stimulus orientation: IL Matching data collected under normal and interferometric viewing conditions

Using an adjustment procedure, human observers matched the apparent spatial frequencies of sinusoidal gratings presented in different orientations (0, 45, 90, and 135 deg). Matches were made between all possible pairwise orientation combinations. Significant match deviations indicated that the apparent frequency of a grating depends on its orientation. The most consistent deviations were found between horizontal and vertical gratings, with horizontal gratings appearing to be of a lower spatial frequency than vertical gratings. These effects were relatively independent of stimulus contrast and persisted when the optics of the eye were bypassed with laser interferometry. A neurophysiological explanation of these effects is proposed.     

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.     

Apparent contrast of suprathreshold gratings varies with stimulus orientation

Human contrast sensitivity is known to vary with both stimulus spatial frequency and orientation. Previous research has indicated, however, that the apparent contrast of a sinusoidal grating is independent of spatial frequency at suprathreshold levels. We have found that the apparent contrast of suprathreshold gratings is not independent of its orientation. Observers adjusted the apparent contrasts of vertical and oblique gratings to match a 40% standard. Contrast match deviations were found at a number of spatial frequencies, indicating a lack of contrast constancy with stimulus orientation. The apparent contrast of gratings in different orientations could not be predicted in any simple fashion from either contrast threshold differences or ratios.     

The directional tuning of the barber-pole illusion.

In order to study the integration of local motion signals in the human visual system, we measured directional tuning curves for the barber-pole illusion by varying two crucial aspects of the stimulus layout independently across a wide a range in the same experiment. These were the orientation of the grating presented behind the rectangular aperture and the aspect ratio of the aperture, which in combination determine the relative contributions of local motion signals perpendicular to the gratings and parallel to the aperture borders, respectively. The strength of the illusion, ie the tendency to perceive motion along the major axis of the aperture, obviously depends on the spatial layout of the aperture, but also on grating orientation. Subjects were asked which direction they perceived and how compelling their motion percept was, revealing different strategies of the visual system to deal with the barber-pole stimulus. Some individuals respond strongly to the unambiguous motion information at the boundaries, leading to multistable percepts and multimodal distributions of responses. Others tend to report intermediate directions, apparently being less influenced by the actual boundaries. The general pattern of deviations from the motion direction perpendicular to grating orientation--a decrease with aspect ratio approaching unity (ie square-shaped apertures) and with gratings approaching parallel orientation to the shorter aperture boundary--is discussed in the context of simple phenomenological models of motion integration. The best fit between model predictions and experimental data is found for an interaction between two stimulus parameters: (i) cycle ratio, which is the sine-wave gratings equivalent of the terminator ratio for line gratings, describing the effects from the aperture boundaries, and (ii) the grating orientation, responsible for perpendicular motion components, which describes the influence of motion signals from inside the aperture. This suggests that the most simple cycle (terminator) ratio explanation cannot fully account for the quantitative properties of the barber-pole illusion.     

The effect of orientation in binocular contour rivalry of real images and afterimages

Binocular rivalry was investigated using gratings of different orientations in three experiments. No consistent effects of orientation were found for predominance measures of rivalry between real images. Rivalrous afterimages, on the other hand, did exhibit orientation selectivity: vertical gratings were visible for longer than were 45-deg gratings. This effect was compared to the similar orientation selectivity found for monocular observation of grating afterimages. Comparisons of binocular rivalry between real images and afterimages were made in terms of the frequency distributions of the dominance periods.     

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.     

Orientation-selective adaptation to crowded illusory lines

Visual adaptation has been successfully used as a psychophysical tool for studying the functional organisation of visual awareness. It has been shown that orientation-selective adaptation to a grating pattern occurs in crowded conditions. In such conditions, simultaneous presentation of flanking distractors pushes the target stimulus out of conscious perception and severely impairs orientation discrimination in the periphery of the visual field. In the present study, orientation-selective adaptation to illusory lines induced by two line gratings abutting each other with a phase shift was examined in crowded and non-crowded conditions. To rule out the effects of lower level adaptations we used an animation paradigm in which the orientations of the two line gratings were altered repeatedly during adaptation phase without any change in the orientation of the resulting illusory line. Although performance of subjects in reporting the orientation of crowded illusory lines was at chance level, orientation-selective adaptation was preserved for crowded as well as non-crowded adapting targets. Two control experiments demonstrated that adaptation to endpoints of real lines at the location of abutting grating lines had minimal effect on the adaptation to illusory lines; and changes in the configuration of endpoints could not be responsible for better performance when adapting and test stimuli were different. We conclude that a crowding effect occurs after illusory lines have been processed in the visual stream. Since illusory lines seem to be represented at relatively early stages of visual processing (e.g. area V2), adaptation to crowded illusory stimuli suggests that neuronal activation in those early stages is not necessarily correlated with conscious perception.     

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.     

眼跳的双相调节理论的行为证据

为了研究眼跳的双相调节理论是否适用于人类的视觉系统,本研究测量了人类被试对分别呈现在三种眼跳时间段（基线、眼跳抑制和眼跳增强）内的光栅的朝向辨别准确率。研究发现：相对于光栅呈现在基线时间段内,被试对呈现在抑制（或增强）时间段内的光栅的朝向辨别准确率显著地更低（或更高）（实验1）;另外,只有使用低或中等空间频率光栅作为测试刺激时,才有这种双相调节作用（实验2）。这些结果表明：人类的视觉系统在眼跳过程中存在双相调节机制,并且这种双相调节机制具有刺激选择性。     

Motion adaptation from surrounding stimuli.

When a narrow uniform gap was surrounded by a moving grating, the gap appeared as a grating in the opposite phase to that of the surround, moving in the same direction with the same speed. Contrast thresholds for moving test-gratings placed in the region of the uniform gap were found to be elevated after prolonged viewing of this pattern, thus demonstrating the existence of motion adaptation in a retinal region surrounded by, but not covered by, a moving pattern. The amplitude of the moving induced-grating was measured by nulling with a real grating moving in the same direction and with the same speed as the surround. When the speed of the inducing grating was varied, the amplitude of the induced effect did not correlate with the magnitude of the threshold elevation. Therefore, it is unlikely that motion adaptation in the uniform gap was due to induced gratings. In some conditions, the adaptation effect of surrounding gratings was no less than the adaptation effect of gratings covering the test region. This result rules out an explantation involving scattered light, and indicates that motion adaptation occurs at a later stage than that consisting of simple motion mechanisms which confound the contrast and velocity of a moving stimulus.     

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.     

Spatial disinhibition of orientation analyzers

Following the successive presentation of two masking gratings (M1 and M2), subjects were required to detect the presence or absence of a single vertical line (TS). When the orientations of the two masks were optimal, M1 was able to reduce the masking effect of M2 on the TS. For a vertical TS, disinhibition was maximal when the orientations of M1 and M2 were similar and was minimal when the orientational difference was greater than 15 deg. It is suggested that the spatial selectivity of the disinhibition function reflects the activity of neurons tuned to orientation, and that the disinhibition masking paradigm may be a useful psychophysical technique to measure tuning functions of other feature detectors.     

Orientation and spatial frequency effects on linear afterimages

Single lines and gratings oriented vertically or at 45 deg were observed as prolonged afterimages in two experiments. The duration of complete visibility exhibited consistent orientation selectivity for the gratings but not for single lines: vertical gratings were visible for longer than were 45-deg gratings. The results are discussed in relation to the hypothesized spatial frequency channels in the human visual system.     

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.     

A severe capacity limit in the consolidation of orientation information into visual short-term memory

Previous research has suggested that two color patches can be consolidated into visual short-term memory (VSTM) via an unlimited parallel process. Here we examined whether the same unlimited-capacity parallel process occurs for two oriented grating patches. Participants viewed two gratings that were presented briefly and masked. In blocks of trials, the gratings were presented either simultaneously or sequentially. In Experiments 1 and 2, the presentation of the stimuli was followed by a location cue that indicated the grating on which to base one’s response. In Experiment 1, participants responded whether the target grating was oriented clockwise or counterclockwise with respect to vertical. In Experiment 2, participants indicated whether the target grating was oriented along one of the cardinal directions (vertical or horizontal) or was obliquely oriented. Finally, in Experiment 3, the location cue was replaced with a third grating that appeared at fixation, and participants indicated whether either of the two test gratings matched this probe. Despite the fact that these responses required fairly coarse coding of the orientation information, across all methods of responding we found superior performance for sequential over simultaneous presentations. These findings suggest that the consolidation of oriented gratings into VSTM is severely limited in capacity and differs from the consolidation of color information.     

Monkeys show an oblique effect.

Monkeys aligned a cursor bar with high-contrast square-wave gratings presented in a variety of orientations. Alignment time increased with increasing spatial frequency from 6 to 24 cycles deg-1 regardless of the orientation of the grating. At higher spatial frequencies, alignment tasks took longer for obliquely oriented gratings than for horizontal and vertical ones. Reducing grating contrast by blurring the image of the 24 cycle deg-1 grating also produced longer alignment times for the obliques. These data indicate that monkeys have an oblique effect similar to that found in humans, implying that the monkey is a useful animal model for investigating the development of meridional anisotropies.     

Psychophysical evidence for an extrastriate contribution to a pattern-selective motion aftereffect

A stationary vertical test grating appears to drift to the left after adaptation to an inducing grating drifting to the right, this being known as the motion aftereffect (MAE). Pattern-specific motion aftereffects (PSMAEs) induced by superimposed pairs of gratings in which the component gratings drift up and down but the observer sees a single coherent plaid drifting to the right have been investigated. Two experiments are reported in which it is demonstrated that the PSMAE is tuned more to the motion of the pattern than to the orientation and direction of motion of the component gratings. However, when subjects adapt to the component gratings in alternation, aftereffect magnitude is dependent upon the individual grating orientations and motion directions. These results can be interpreted in terms of extrastriate contributions to the PSMAE, possibly arising from the middle temporal area, where some cells, unlike those in striate cortex (V1), are tuned to pattern motion rather than to component motion.     

光栅朝向分辨学习中存在关于45°对角线对称的镜像迁

采用光栅朝向分辨任务来探讨视知觉学习中是否存在关于45°对角线对称的镜像迁移现象。训练被试分辨15°或75°朝向3或5天,每天约1小时,训练前后测量15°、75°、45°朝向的分辨阈值。通过训练,训练朝向（15°或75°）的阈值下降,该学习效应没有迁移至45°朝向,但基本迁移到关于45°对称的朝向（75°或15°）上。这提示,视知觉学习可能发生在中间视皮层,该皮层同时具有一定的朝向特异性和关于45°对角线对称的镜像迁移性