Binocular rivalry with moving patterns

Binocular rivalry between a horizontal and a vertical grating was examined in six experiments. The gratings could be presented in a static form or dynamically so that either one or both gratings moved. The motion consisted of a symmetrical transformation of the gratings about their centers, so that the lines moved outwards or inwards. During rivalry, a moving pattern was visible for about 50% longer than an equivalently oriented static pattern (Experiments 1, 2, and 4). When both gratings were in motion (Experiments 3 and 5), the course of rivalry was similar to that found for two static gratings. The duration of dominance of the moving grating was influenced by its velocity (Experiment 6). The results are interpreted in terms of the stimulus strengths of the static and dynamic patterns.     

The orientation anisotropy and orientation constancy: a visual evoked potential study.

Two experiments were conducted on the orientation anisotropy in which averaged visual evoked potentials (VEPs) were recorded from the occipital scalp. The first experiment confirmed the findings of Maffei and Campbell (1970) that obliquely oriented gratings alternated back and forth produced smaller-amplitude VEPs than when the gratings were oriented horizontally or vertically. Since no asymmetry was found in VEPs produced by a Julesz figure presented under identical conditions, it was concluded that direction of displacement could not have been contributing to the effect. In a second experiment head tilt of the subject was manipulated together with grating orientation and the results indicated that the orientation anisotropy is retinally rather than gravitationally referenced. It was concluded that the site of orientation constancy is located either at higher levels of the primary visual system or in the second visual system.     

The temporal course of suppression during binocular rivalry

Orthogonally oriented sinusoidal luminance gratings were dichoptically presented to the observers' left and right eyes. During the subsequent binocular rivalry, a small target was briefly presented (4AFC) to probe the strength of interocular suppression at various temporal latencies. Both stationary and moving rivalrous patterns were investigated. The purpose of experiment 1 was to compare the temporal characteristics of stationary and motion rivalry (0 and 1.2 deg s-1), while that of experiment 2 was to examine rivalry suppression for higher speeds (2 and 4 deg s-1). In all cases, it was found that the strength of suppression remained essentially constant throughout a single phase of binocular rivalry. The results of the investigation also revealed that moving rivalrous patterns lead to greater magnitudes of interocular suppression than static patterns. Despite these differences in the strength of suppression, the results of both experiments show that the temporal characteristics of motion and static rivalry are essentially identical.     

Contrast and spatial frequency components in visual preferences of newborns

A preferential-looking procedure was used to investigate newborns' responses to square-wave gratings varying in spatial frequency and contrast. A preliminary study confirmed that the gratings used in the experiment were suprathreshold. In the experiment newborns' preference for a grating of 0.1 cycle deg-1 within the peak contrast sensitivity range was examined. Reduction in the contrast of this grating led to a transfer of the preference to a high-contrast grating of the same space-averaged luminance with a spatial frequency outside this range (0.42 cycle deg-1). The findings are discussed with reference to the role of the contrast sensitivity function in pattern preferences of newborns: it is suggested that contrast and spatial frequency interact in determining pattern preferences.     

Binocular interactions in suprathreshold contrast perception

Suprathreshold binocular contrast interactions were studied psychophysically. A split-screen CRT display was used to present separate sine-wave gratings to the observer’s left and right eyes. The method of constant stimuli and a modified method of adjustment were used to find sets of binoculartest patterns that matched a given binocularstandard. Test patterns consisted of the simultaneous presentation of sine-wave gratings that differed in contrast to the left and right eyes. Standard patterns consisted of identical sine-wave gratings presented to the two eyes, and had the same spatial frequency as the test patterns. Binocular contrast matching functions were obtained for several standard contrasts at 1 and 8 c/deg. Binocular matching functions were obtained for luminance increments as well. The binocular contrast matching functions departed from a simple binocular averaging rule, and behaved as if the eye receiving the higher contrast disproportionately dominated the binocular contrast percept. Departures from the binocular averaging rule were slightly greater for higher standard contrasts. Spatial frequency had little effect, and the luminance increment matching functions also departed from the binocular averaging rule. There was evidence for a contrast version of Fechner’s paradox and for substantial individual differences in a form of ocular dominance. In a further experiment, additivity of suprathreshold binocular contrast summation was examined by testing the double-cancellation condition. We found no systematic violations of additivity at 1 and 8 c/deg. Models of suprathreshold binocular contrast summation were examined.     

Motion over the retina and the motion aftereffect.

The motion aftereffect (MAE) was measured with retinally moving vertical gratings positioned above and below (flanking) a retinally stationary central grating (experiments 1 and 2). Motion over the retina was produced by leftward motion of the flanking gratings relative to the stationary eyes, and by rightward eye or head movements tracking the moving (but retinally stationary) central grating relative to the stationary (but retinally moving) surround gratings. In experiment 1 the motion occurred within a fixed boundary on the screen, and oppositely directed MAEs were produced in the central and flanking gratings with static fixation; but with eye or head tracking MAEs were reported only in the central grating. In experiment 2 motion over the retina was equated for the static and tracking conditions by moving blocks of grating without any dynamic occlusion and disclosure at the boundaries. Both conditions yielded equivalent leftward MAEs of the central grating in the same direction as the prior flanking motion, ie an MAE was consistently produced in the region that had remained retinally stationary. No MAE was recorded in the flanking gratings, even though they moved over the retina during adaptation. When just two gratings were presented, MAEs were produced in both, but in opposite directions (experiments 3 and 4). It is concluded that the MAE is a consequence of adapting signals for the relative motion between elements of a display.     

Thresholds for movement direction: Two directions are less detectable than one

Thresholds for detecting movement direction were measured for two different types of dynamic dot display; first, one in which all dots moved upwards, and secondly, one in which half the dots moved upwards and half moved downwards. Direction sensitivity was found to be worse for the stimulus containing two simultaneous directions of motion than for the stimulus in one direction. These data are taken as evidence of some form of competition, or AND-NOT gating, between the outputs of direction-specific analysers during threshold determination.     

Purely chromatic perception of motion in depth: two eyes as sensitive as one

Motion hyperacuity (phase) thresholds were measured for both lateral and stereoscopic oscillatory motion in both luminance and equiluminant red/green gratings of 2 cycles per degree. Thresholds for lateral chromatic motion did not exhibit the inhibitory fall-off at low temporal frequencies that was found for luminance motion. Phase thresholds for purely chromatic motion were substantially higher than those for luminance gratings, in proportion to the ratio of cone signal modulation, but they could be predicted from the corresponding contrast sensitivities for both types of stimulus. Stereomovement thresholds in luminance gratings showed the stereomovement suppression effect relative to monocular motion sensitivity previously reported for line stimuli, but purely chromatic gratings did not. Together with the lack of an inhibitory fall-off, these results imply that chromatic and luminance motion are processed by different neural pathways, and that the chrominance pathway is capable of supporting a strong percept of stereoscopic motion from purely chromatic gratings.     

Effective luminance contrast as a parameter in contingent aftereffects

Variation in the magnitude of contingent aftereffects was explored as a function of the luminance contrast ratio profile of inspection stimuli. Positive contrast stimuli (chromatic bars interspersed with achromatically brighter bars) produced substantially attenuated aftereffects compared with negative contrast stimuli (chromatic and dark bars). This attenuation was hypothesized to result from retinal image deterioration of positive contrast gratings due to retinal reflection/scatter. In a second experiment, subjects selected for their light retinal pigmentation manifested substantial enhancement of the asymmetry between the aftereffects generated by positive and negative contrast gratings. Those with dark fundus pigmentation showed symmetrical aftereffects.     

The hollow-face illusion: object-specific knowledge, general assumptions or properties of the stimulus?

The hollow-face illusion, in which a mask appears as a convex face, is a powerful example of binocular depth inversion occurring with a real object under a wide range of viewing conditions. Explanations of the illusion are reviewed and six experiments reported. In experiment 1 the detrimental effect of figural inversion, evidence for the importance of familiarity, was found for other oriented objects. The inversion effect held for masks lit from the side (experiment 2). The illusion was stronger for a mask rotated by 90 degrees lit from its forehead than from its chin, suggesting that familiar patterns of shading enhance the illusion (experiment 2). There were no effects of light source visibility or any left/right asymmetry (experiment 3). In experiments 4-6 we used a 'virtual' hollow face, with illusion strength quantified by the proportion of noise texture needed to eliminate the illusion. Adding characteristic surface colour enhanced the illusion, consistent with the familiar face pigmentation outweighing additional bottom-up cues (experiment 4). There was no difference between perspective and orthographic projection. Photographic negation reduced, but did not eliminate, the illusion, suggesting shading is important but not essential (experiment 5). Absolute depth was not critical, although a shallower mask was given less extreme convexity ratings (experiment 6). We argue that the illusion arises owing to a convexity preference when the raw data have ambiguous interpretations. However, using a familiar object with typical orientation, shading, and pigmentation greatly enhances the effect.     

The spatial spread of attentional modulation of the motion aftereffect

The spatial spread of attentional modulation of selective adaptation was investigated in four experiments in which the duration of the movement aftereffect (MAE) was measured with and without processing of intermittently changing digits at the fixation point. In the first experiment, the effects of diverting attention on MAE duration were found to reduce as the distance between the fixation digits and the inner edge of the surrounding adapt/test grating was increased. A second experiment suggested that eye movements were unlikely to underlie the attentional effects. In experiment 3, the attentional effect stayed constant as the outer diameter of the adapt/test gratings was increased. In experiment 4 (as in experiment 1) the modulatory effects of attention were larger the closer the adapt/test gratings were to the locus of attention, when the area of the grating was held constant but its eccentricity varied. In experiments 1 and 4, an intermittently changing fixation digit was found to reduce MAE durations more than an unchanging digit, even when subjects were not required to process it, suggesting that exogenous as well as endogenous attentional processes modulate early motion processing.     

Coordination Dynamics of the Bipedal Galloping Pattern

A motion equation in relative phase was developed that incorporates the spatial-temporal pattern of the bipedal gallop along with the more commonplace patterns of the bipedal jump and walk-run. In 3 experiments, human participants (N = 6 per experiment) simulated the bipedal gait patterns through the rhythmic motions of hand-held pendulums. Predictions of the motion equation for coordination equilibria and their respective degrees of stability were confirmed. In particular, the gallop pattern was less stable than the fundamental in-phase and antiphase patterns but changed in qualitatively similar ways to those gaits as a function of limb asymmetry and movement frequency. The relation between the modeled coordination dynamics and the kinematic characteristics of real bipedal galloping is discussed     

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。     

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.     

Preference for symmetry is experience dependent in newborn chicks (Gallus gallus)

Spontaneous pecking preferences toward symmetric or asymmetric stimuli were tested in newborn chicks (Gallus gallus). A preference for asymmetric patterns was found in na?ve chicks (either 24 or 48 hours old), although a preference for symmetry appeared at retest after chicks had experienced standard rearing conditions (Experiments 1 and 2). Only food-experienced chicks preferred symmetric patterns; food-deprived and hand-fed chicks did not show any preference (Experiment 3). A key factor that allowed for the emergence of a preference for symmetry may relate to the improving of pecking sensorimotor skills occurring during active food manipulation. Possible explanations are discussed for the late emergence of the preference for symmetry and for the preference for asymmetry found in na?ve chicks.     

Coordination Dynamics of the Bipedal Galloping Pattern

A motion equation in relative phase was developed that incorporates the spatial-temporal pattern of the bipedal gallop along with the more commonplace patterns of the bipedal jump and walk-run. In 3 experiments, human participants (N = 6 per experiment) simulated the bipedal gait patterns through the rhythmic motions of hand-held pendulums. Predictions of the motion equation for coordination equilibria and their respective degrees of stability were confirmed. In particular, the gallop pattern was less stable than the fundamental in-phase and antiphase patterns but changed in qualitatively similar ways to those gaits as a function of limb asymmetry and movement frequency. The relation between the modeled coordination dynamics and the kinematic characteristics of real bipedal galloping is discussed.     

Motion perception in the ageing visual system: minimum motion, motion coherence, and speed discrimination thresholds

We aimed to address two issues: first, to describe how the perception of motion differs in elderly observers as compared to younger ones; and, second, to see if these changes in motion perception could be accounted for by the known changes in the ability of elderly observers to detect patterns (as indexed via contrast sensitivity). The lower threshold of motion, motion coherence, and speed discrimination were measured, alongside contrast sensitivity, in a group of thirty-two older (mean age 61.5 years) and thirty-two younger (mean age 23.2 years) subjects. The older observers showed losses in their ability to detect slow motions as indexed via the lower threshold of motion for random-dot patterns and for gratings of a range of spatial frequencies. They also were impaired on a test of motion coherence, but only for stimuli of a slow to medium speed, whereas faster speeds showed no decline with age. Finally, at all speeds tested the older observers required greater differences in speed in order to discriminate between patterns moving at different speeds. The pattern of losses on motion perception tasks was not predicted by the deficits of the older groups, such as loss of detection thresholds for high spatial and/or temporal frequencies. It is concluded that these hypotheses do not provide an adequate account of the data, and therefore that the losses occurring with age are complex and probably are a result of the loss of several types of cell.     

Floral guidance of learning a preference for symmetry by bumblebees

This study examines the mechanism underlying one way in which bumblebees are known to develop a preference for symmetric patterns: through prior non-differential reinforcement on simple patterns (black discs and white discs). In three experiments, bees were given a choice among symmetric and asymmetric black-and-white non-rewarding patterns presented at the ends of corridors in a radial maze. Experimental groups had prior rewarded non-discrimination training on white patterns and black patterns, while control groups had no pre-test experience outside the colony. No preference for symmetry was obtained for any of the control groups. Prior training with circular patterns highlighting a horizontal axis of symmetry led to a specific subsequent preference for horizontal over vertical symmetry, while training with a vertical axis abolished this effect. Circles highlighting both axes created a general avoidance of asymmetry in favour of symmetric patterns with vertical, horizontal or both axes of symmetry. Training with plain circles, but not with deformed circles, led to a preference for symmetry: there was no evidence that the preference emerged just by virtue of having attention drawn away from irrelevant pattern differences. Our results point to a preference for symmetry developing gradually through first learning to extract an axis of symmetry from simple patterns and subsequently recognizing that axis in new patterns. They highlight the importance of continued learning through non-differential reinforcement by skilled foragers. Floral guides can function not only to guide pollinators to the source of reward but also to highlight an axis of symmetry for use in subsequent floral encounters.     

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.     

The development of contrast constancy

The mature visual system possesses mechanisms that enable invariant perception of the contrast of an object and its features as the object undergoes changes in distance. This phenomenon, which has been called contrast constancy, obtains at suprathreshold contrasts only. Some models of contrast constancy assume the presence of narrowband spatial-frequency channels. An implication of M.S. Banks, B.R. Stephens, and E.E. Hartmann (1985, Journal of Experimental Child Psychology, 40, 501-527) is that contrast constancy should not be observed at 6 weeks but may be observed at 12 weeks. We examined this implication by investigating the development of contrast constancy in 6- and 12-week-old infants. Two sine wave gratings, differing in spatial frequency by a factor of 3, were presented side-by-side. The contrast of one grating was varied in order to estimate the contrast at which preference for the two gratings was equal. The equal preference points for 6-week-olds were predictable from their contrast thresholds. The 12-week-olds' equal preference points for low-contrast stimuli were predictable from their contrast thresholds, but those for intermediate and high-contrast stimuli were not. Thus, if one accepts the assumption that equal preference in infants is analogous to apparent contrast matches in adults, these data imply that contrast constancy is observed at 12 weeks but not 6 weeks. The perceptual consequences of this developmental transition are discussed.