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.     

Discriminative performance of the domestic hen in a visual acuity task

The performance of 6 domestic hens on a visual acuity task was studied using a spatial discrete-trial conditional discrimination procedure. Gray stimuli and vertical square-wave gratings, ranging in spatial frequency from 1 to 10 cycles per millimeter, were presented in a descending and ascending series of probes. On each trial, either a grating or gray stimulus was presented. Only one spatial frequency of grating was presented during each session. Between probe sessions, training continued at the coarsest grating value. Stimulus discriminability, measured as values of log d, changed with changes in grating spatial frequency for both probe series. Fitted lines described the linear portion of the psychometric functions. Thresholds estimated from the lines generally ranged from four to six cycles per degree, with slightly greater estimates from data from the descending probe series. There were no systematic changes in response bias as a function of grating spatial frequency.     

Binocular rivalry and surface-boundary processing

Theoretical and empirical studies show that the visual system relies on boundary contours and surface features (e.g. textures) to represent 3-D surfaces. When the surface to be represented has little texture information, or has a periodic texture pattern (grating), the boundary contour information assumes a larger weight in representing the surface. Adopting the premise that the mechanisms of 3-D surface representation also determine binocular rivalry perception, the current paper focuses on whether boundary contours have a similar role in binocular rivalry. In experiment 1, we tested the prediction that the visual system prefers selecting an image/figure defined by boundary contours for rivalry dominance. We designed a binocular rivalry stimulus wherein one half-image has a boundary contour defined by a grating disk on a background with an orthogonal grating orientation. The other half-image consists solely of the (same orientation) grating background without the grating disk, ie no boundary contour. Confirming our prediction, the predominance for the half-image with the grating disk is approximately 90%, despite the fact that the grating disk corresponds to an area with orthogonal grating in the fellow eye. The advantage of the grating disk is dramatically reduced to about 50% predominance when a boundary contour is added to the background-only half-image at the location corresponding to the grating disk. We attribute this reduced advantage to the formation of a corresponding binocular boundary contour. In experiment 2 the grating background was substituted by a random-dot background in a similar stimulus design. We found that the perceptual salience of the corresponding binocular boundary contours extracted by the interocular matching process is an important factor in determining the dynamics of binocular rivalry. Experiment 3 showed that vertical lines with uneven thickness and spacing as the background reduce the contribution of the monocular boundary contour of the grating disk in binocular rivalry, possibly through the formation of binocular boundary contours between the local edges (vertical components) of the vertical lines and the corresponding grating disk.     

The site of binocular rivalry suppression.

Two experiments were performed to localize the site of binocular rivalry suppression in relation to the locus of grating adaptation. In one experiment it was found that phenomenal suppression of a high-contrast adaptation grating presented to one eye had no influence on the strength of the threshold-elevation aftereffect measured interocularly. Evidently information about the adaptation grating arrives at the site of the aftereffect (presumably binocular neurons) even during suppression. In a second experiment 60 s of grating adaptation was found to produce a short-term reduction in the predominance of the adapted eye during binocular rivalry. These findings provide converging lines of evidence that suppression occurs at a site in the human visual system after the locus of grating adaptation and, hence, after the striate cortex.     

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.     

A new visual illusion, and its mechanism

A new visual illusion is reported, in which a sine-wave grating appears to tilt when doubly sheared perpendicularly to the grating lines. It is shown that the illusory percept is related to the Münsterberg and Café Wall illusions. The probable mechanism at the root of all such illusions is postulated by reference to the neuroarchitecture of the retina and striate cortex.     

Multidimensional encoding of visual form

The encoding of stimulus dimensions of visual form in the human S was investigated under conditions of threshold exposure durations. Three stimulus dhnensions defined on a spatial grating were investigated: spatial line frequency, grating orientation, and orientation of a transverse break in the lines of grating. Results support the conclusion that, within the general category of visual form, different primary stimulus dimensions such as spatial frequency and orientation may be encoded simultaneously, whereas, when the two stimulus components for report are defined on the same dimension (orientation), overall performance is consistent with the predictions of a single channel model.     

The role of voluntary and involuntary attention in selecting perceptual dominance during binocular rivalry

When incompatible images are presented to corresponding regions of each eye, perception alternates between the two monocular views (binocular rivalry). In this study, we have investigated how involuntary (exogenous) and voluntary (endogenous) attention can influence the perceptual dominance of one rival image or the other during contour rivalry. Subjects viewed two orthogonal grating stimuli that were presented to both eyes. Involuntary attention was directed to one of the grating stimuli with a brief change in orientation. After a short period, the cued grating was removed from the image in one eye and the uncued grating was removed from the image in the other eye, generating binocular rivalry. Subjects usually reported dominance of the cued grating during the rivalry period. We found that the influence of the cue declined with the interval between its onset and the onset of binocular rivalry in a manner consistent with the effect of involuntary attention. Finally, we demonstrated that voluntary attention to a grating stimulus could also influence the ongoing changes in perceptual dominance that accompany longer periods of binocular rivalry Voluntary attention did not increase the mean dominance period of the attended grating, but rather decreased the mean dominance period of the non-attended grating. This pattern is analogous to increasing the perceived contrast of the attended grating. These results suggest that the competition during binocular rivalry might be an example of a more general attentional mechanism within the visual system.     

Accuracy of aiming in linear hand-movements

Six subjects took part in an experiment which consisted of drawing, in a horizontal plane, a number of lines of different lengths and in different directions. The lines were drawn from a starting-point towards a target-point, and the instructions and previous practice were designed to ensure that the lines were drawn in one movement without appreciable amendment during the drawing. The direction and length of the lines were both found to affect the accuracy of aiming, and certain directions showed a persistent bias in the distribution of their errors. Closing the eyes just prior to and during the drawing of the lines had the result of diminishing the effect of changes in direction and length, but it increased the bias. In attempting a theoretical analysis of the results, some of the limitations imposed by human anatomy have been considered in an elementary way. The general conclusion is that, in this task, the effects of altering length, of altering direction and of opening or closing the eyes can, to a great extent, be plausibly ascribed to the particular anatomical nature of the human operator, provided one makes certain simple assumptions about the theory of movement control.     

Drawing the net: internet identification, internet use, and the image of internet users.

Theory and research suggest that Internet identification may account for some of the gender divide in Internet use. Internet identification is a type of domain identification, and is inherently bound with images of those who use the Internet, a domain traditionally conceived as masculine. Combining the "draw an Internet user" test with an Internet identification scale, this study tests two hypotheses: participants drawing gender-concordant images will (i) identify with and (ii) use the Internet more than those drawing gender-discordant images. Participants were 371 students (121 males, 250 females) from three universities in the United Kingdom and Australia. The need to challenge masculinized images of the Internet is discussed.     

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.     

Variations in apparent spatial frequency with stimulus orientation: L Incidence of the effect in the general population

The human visual system is anisotropic not only for stimulus detection and discrimination but also for stimulus appearance. The apparent length of a stationary stimulus and the apparent velocity of a moving stimulus vary with orientation. These variations are predictable from a model assuming a compression of the horizontal spatial meridian relative to the vertical meridian. In this paper, the apparent spatial frequency of a suprathreshold grating is shown to depend on the grating orientation. Specifically, horizontal gratings appear coarser than vertical gratings of equivalent spatial frequency. Additional data collected from the same group of observers show that horizontal lines appear shorter than vertical lines of the same extent. The presence of the spatial frequency and length illusions, although both predictable from the compression model, were not found to be correlated within observers. Implications of these results for other data in the literature are discussed.     

Pressure blindness and the interocular transfer of size aftereffects

After observation of a stimulus composed of a top grating with large bar widths (low spatial frequency) and a bottom grating of narrow lines (high spatial frequency), a subsequently presented test grating of medium bar width appears to have a higher spatial frequency on the top half than on the bottom. Although this size aftereffect can be obtained dichoptically, this does not necessarily imply a central locus, since retinal input from the adapted eye could produce the effect. Ss were tested for the aftereffect in the adapted eye and for interocular transfer with and without pressure blinding the adapted eye. In this last condition, input from the adapted eye cannot reach the cortex. However, the aftereffect was equally present under all three conditions. This result suggests that size and frequency adaptation have a central locus.     

Contextual modulation of the motion aftereffect

The authors examined center-surround effects for motion perception in human observers. The magnitude of the motion aftereffect (MAE) elicited by a drifting grating was measured with a nulling task and with a threshold elevation procedure. A surround grating of the same spatial frequency, temporal frequency, and orientation significantly reduced the magnitude of the MAE elicited by adaptation to the center grating. This effect was bandpass tuned for spatial frequency, orientation, and temporal frequency. Plaid surrounds but not contrast-modulated surrounds that moved in the same direction also reduced the MAE. These results provide psychophysical evidence for center-surround interactions analogous to those previously observed in electrophysiological studies of motion processing in primates. Collectively, these results suggest that motion processing, similar to texture processing, is organized for the purpose of highlighting regions of directional discontinuity in retinal images.     

Use of 3-dimensional body scans for body-image research

This preliminary study explored the use of highly realistic 3-dimensional body-scan images as a potential tool, taking advantage of a much more specific and expanded representation of the entire body. Traditionally, body-image research makes use of various contour drawing scales whose 2-dimensional figures increase proportionately and do not match the shape of many women. The study tested whether body-scanned images (N = 85) could be consistently "matched" to individual figures on a contour drawing scale. Internal consistency and interrater reliability were calculated and high coefficients were observed (alpha = .97, kappa = .80). The potential of utilizing 3-dimensional images either as more realistic somatotypes in contour-rating scales or as a measurement of body-image satisfaction using computer manipulation of a digital image is discussed.     

The influence of handedness on profile and line drawing directionality in children,young, and older normal adults

One hundred twenty-two normal subjects--children, young and older adults (77 right-handers and 45 left-handers)--performed two drawing tasks in order to study their directionality trends. The first task consisted of drawing the profile of a face and in the second task subjects had to link two points in order to draw a line. The analysis of the drawing directionality revealed a significant effect of the age when right-handers drew profiles whereas this effect reached significance in left-handed subjects only when drawing lines. Left- and right-handers' performances across the two tasks were found to significantly differ. Results are discussed in terms of hemispheric and environmental factors.     

Perceptual differentiation of sequential visual patterns

The aftereffects of viewing diagonal lines for 50, 500, and 1,000 msec were measured by the speed and accuracy of identification of a variably tilted test grating. Significant RT and tilt aftereffects were found as functions of the duration of orientation-specific adaptation and the angle of separation between inspection and test lines. The results throw light on anchoring effects of the main visual coordinates and support a structural interpretation of orientational selectivity in human vision.     

Eye movements in drawing simple lines

As part of an investigation into real-world drawing, eye movements and eye-hand interactions have been recorded for twenty subjects of varying drawing experience drawing simple straight and curved lines and a square. Two modes of eye-hand behaviour were observed. In the first, named 'close pursuit', fixations closely followed the pencil with a sequence of small saccades. In the second, named 'target locking', a stable fixation was made on the end-point of the line throughout the entire drawing action. Depending on subject and type of line, close pursuit, target locking, or a combination of these modes was used regardless of previous drawing experience. The results are discussed in terms of the role of the eye in the control of the movement trajectory of the hand.     

Near-field visual acuity of pigeons: effects of head location and stimulus luminance.

Two pigeons were trained to discriminate a grating stimulus from a blank stimulus of equivalent luminance in a three-key chamber. The stimuli and blanks were presented behind a transparent center key. The procedure was a conditional discrimination in which pecks on the left key were reinforced if the blank had been present behind the center key and pecks on the right key were reinforced if the grating had been present behind the center key. The spatial frequency of the stimuli was varied in each session from four to 29.5 lines per millimeter in accordance with a variation of the method of constant stimuli. The number of lines per millimeter that the subjects could discriminate at threshold was determined from psychometric functions. Data were collected at five values of stimulus luminance ranging from--0.07 to 3.29 log cd/m2. The distance from the stimulus to the anterior nodal point of the eye, which was determined from measurements taken from high-speed motion-picture photographs of three additional pigeons and published intraocular measurements, was 62.0 mm. This distance and the grating detection thresholds were used to calculate the visual acuity of the birds at each level of luminance. Acuity improved with increasing luminance to a peak value of 0.52, which corresponds to a visual angle of 1.92 min, at a luminance of 2.33 log cd/m2. Further increase in luminance produced a small decline in acuity.     

Confusable gratings selectively elicit orientation-contingent colour aftereffects

Induction of orientation-selective colour aftereffects (the McCollough effect) was studied with groups of young children who differed in their ability to discriminate an oblique grating from its mirror-image under recognition conditions. If the McCollough effect is generated through associative learning, children who failed to learn simple identifying responses to oblique lines as a function of the direction in which the lines point should also fail to associate colour lablels selectively to these same stimuli. Instead, the ease with which the McCollough effect was induced by alternate exposure to left-oblique lines in green light and right-oblique lines in red light was independent of the ability of the young child to discriminate direction of line under recognition conditions.