Dichoptic plaids may rival, but their motions can integrate

When the eyes view incompatible images, binocular rivalry usually results: image constituents in corresponding parts of the monocular visual fields are not perceived simultaneously. We asked naive undergraduates to view dichoptic, dioptic, and monoptic plaids. The dichoptic images evoked strong binocular rivalry when contrast was high, especially if the component gratings were set in motion. Nevertheless, the subjects' visual systems integrated the motion information across the two eyes, producing a unitary motion percept that did not reflect the image in either eye alone. By manipulating the relative spatial scale of the gratings, we affected how well the motion cohered: the results were remarkably similar between dichoptic and traditional dioptic plaids. By manipulating the relative speed of the gratings, we systematically affected the perceived direction of motion of the plaids; these results were also remarkably similar for dichoptic and dioptic plaids. Thus, the motion analysis of dichoptic and dioptic plaids is proceeding according to very similar rules, even though the dichoptic images are incompatible and evoke binocular rivalry.     

On the role of attention in binocular rivalry: electrophysiological evidence

During binocular rivalry visual consciousness fluctuates between two dissimilar monocular images. We investigated the role of attention in this phenomenon by comparing event-related potentials (ERPs) when binocular-rivalry stimuli were attended with when they were unattended. Stimuli were dichoptic, orthogonal gratings that yielded binocular rivalry and dioptic, identically oriented gratings that yielded binocular fusion. Events were all possible orthogonal changes in orientation of one or both gratings. We had two attention conditions: In the attend-to-grating condition, participants had to report changes in perceived orientation, focussing their attention on the gratings. In the attend-to-fixation condition participants had to report changes in a central fixation target, taking attention away from the gratings. We found, surprisingly, that attending to rival gratings yielded a smaller ERP component (the N1, from 160-210 ms) than attending to the fixation target. To explain this paradoxical effect of attention, we propose that rivalry occurs in the attend-to-fixation condition (we found an ERP signature of rivalry in the form of a sustained negativity from 210-300 ms) but that the mechanism processing the stimulus changes is more adapted in the attend-to-grating condition than in the attend-to-fixation condition. This is consistent with the theory that adaptation gives rise to changes of visual consciousness during binocular rivalry.     

Orientation acuity estimated with simultaneous and successive procedures.

Orientation discrimination thresholds for medium contrast sinewave grating stimuli were estimated by a forced-choice procedure for the two principal, and the two main oblique axes. The results obtained for simultaneous presentation with a centre/surround stimulus arrangement are compared with the threshold estimates obtained when the two stimuli to be discriminated do not overlap in time. We find that orientation acuity depends on the temporal relationship of the discriminanda. Estimates of orientation threshold with simultaneous presentation are lower on all axes tested than those obtained with successive presentation; the greatest difference in orientation acuity was found at obliques. The data support the hypothesis that the meridional anisotropy in orientation discrimination that is found with conventional, two-interval forced-choice methods is not entirely attributable to anatomical and physiological changes at the level of the striate cortex.     

Size-disparity correlation in human binocular depth perception.

To use the small horizontal disparities between images projected to the eyes for the recovery of three-dimensional information, our visual system must first identify which feature in one eye's image corresponds with which in the other. The earliest level of disparity processing in primates (V1) contains cells that are spatial-frequency tuned. If such cells have a disparity range that covers only a single period of their mean tuning frequency, there will always be exactly one potential match within this range. Here, this 'size-disparity' hypothesis was tested by measuring the contrast sensitivity of stereopsis as a function of disparity for single bandpass-filtered items. It was found that thresholds were low and relatively constant up to disparities an order of magnitude larger than is predicted by this constraint. Furthermore, peak sensitivity was relatively independent of spatial frequency. A control experiment showed that binocular correlation of the carrier is necessary for this task. In a third experiment, the maximum disparity that supports threshold performance was compared for an isolated bandpass item and bandpass-filtered noise. This limit was found to be five times larger for the isolated stimuli. In summary, these findings show that the initial stage of disparity detection is not limited by the size-disparity constraint. For stimuli with multiple false targets, however, processes subsequent to this stage reduce the disparity range over which the correspondence problem can be solved.     

Effects of Texture Component Orientation on Orientation Flow Visibility for 3-D Shape Perception

In images of textured 3-D surfaces, orientation flows created by the texture components parallel to the surface slant play a critical role in conveying the surface slant and shape. This study examines the visibility of these orientation flows in complex patterns. Specifically, we examine the effect of orientation of neighboring texture components on orientation flow visibility. Complex plaids consisting of gratings equally spaced in orientation were mapped onto planar and curved surfaces. The visibility of the component that creates the orientation flows was quantified by measuring its contrast threshold (CT) while varying the combination of neighboring components present in the pattern. CTs were consistently lowest only when components closest in orientation to that of the orientation flows were subtracted from the pattern. This finding suggests that a previously reported frequency-selective cross-orientation suppression mechanism involved with the perception of 3-D shape from texture is affected by proximity in orientation of concurrent texture components.     

Release from Cross-Orientation Suppression Facilitates 3D Shape Perception

Cross-orientation suppression (COS) in striate cortex has been implicated in the efficient encoding of visual stimuli. We show that release from COS facilitates the decoding of 3-D shape. In planar surfaces overlaid with textures, slanting the surface can increase the visibility of the component parallel to the slant. Since this component provides the orientation flows that signify 3-D shape, the enhancement of visibility facilitates 3-D slant perception. Contrast thresholds reveal that this enhancement results from a decrease in COS when 3-D slant creates a frequency mismatch between texture components. We show that coupling compressive nonlinearities in LGN neurons with expansive nonlinearities in cortical neurons can model the frequency-specific component of suppression.     

Contrast discrimination and choice reaction times at near-threshold pedestals

Choice reaction times (CRTs) to contrast differences were measured and compared with contrast increment thresholds obtained from concurrently measured psychometric functions at pedestal contrasts in the vicinity of detection threshold. Contrast discrimination functions had a classical dipper shape. The main finding was that CRTs were shorter at low pedestal contrasts but longer at higher pedestal contrasts compared to detection, reflecting the behaviour of increment thresholds. Even when equalized for response accuracy, CRTs varied with pedestal contrast in a similar manner to the contrast increment thresholds. The finding that CRTs and contrast increment thresholds depended on pedestal contrast in a similar manner suggests that both share a common origin. This common origin is proposed to lie in the variability of the sensory effect which determines the variability of the information accumulation process, which in turn affects the response criterion and contrast increment thresholds. At low pedestals, a decrease in variability lowers thresholds and results in a lower response criterion, thereby accelerating reaction times. At high pedestals, increasing signal-dependent noise inflates variability and thus raises thresholds and the response criterion, which results in slower CRTs.     

Probing depth in monocular images

It is generally expected that depth (distance) is the internal representational primitive that corresponds to much of the perception of 3D. We tested this assumption in monocular surface stimuli that are devoid of distance information (due to orthographic projection and the chosen surface shape, with perspective projection used as a control) and yet are vividly three-dimensional. Slant judgments were found to be in close correspondence with the actual geometric slant of the stimuli; the spatial orientation of the surfaces was perceived accurately. The apparent depth in these stimuli was then tested by superimposing a stereo depth probe over the monocular surface. In both the perspective and orthographic projection the gradient of perceived depth, measured by matching the apparent depth of the stereo probe with that of the monocular surface at a series of locations, was substantial. The experiments demonstrate that in orthographic projection the visual system can compute from local surface orientation a depth quantity that is commensurate with the relative depth derived from stereo disparity. The depth data suggests that, at least in the near field, the zero value for relative depth lies at the same absolute depth as the stereo horopter (locus of zero stereo disparity). Relative to this zero value, the depth-from-slant computation seems to provide an estimate of distance information that is independent of the absolute distance to the surface.Supproted by Office of Naval Research Contract N00014-K-84-0533. We gratefully acknowledge the suggestions of Jacob Beck regarding the experimental design, and the assistance provided by Cathryn Stanford     

朝向和对比度同时快速变化条件下的分辨能力

在自然的视觉中,投射到视网膜上的视觉图像总是在不停地变化,而人类的感知系统依然可以准确高效地识别物体.因此,人类的感知系统有相应的快速处理机制以应对这种动态变化．然而,前人的实验都是在相对稳定的刺激条件下研究人类被试的感知系统对一个刺激参数的反应,比如在固定对比度下测试朝向分辨能力,或在固定朝向测定对比度分辨能力,而朝向和对比度同时变化时,人类对这两个参数的分辨能力仍然缺乏研究．因此,在本实验中,我们使用朝向和对比度同时变化的刺激,研究了人类被试对朝向和对比度的分辨能力．结果表明,在这种动态变化的条件下,被试对朝向和对比度的分辨阈值都有显著性的降低．而且,朝向分辨阈值降低的幅度与在固定对比度参数条件下的分辨阈值成负相关,即在固定对比度条件下朝向分辨阈值较高的被试,在朝向和对比度同时变化条件下,其朝向分辨阈值降低的幅度相对要大,朝向分辨能力也就相对地提高更大．对比度分辨能力也呈现同样的规律．这些结果说明,朝向和对比度的同时变化提高了被试对朝向和对比度的分辨能力,一个参数变化时其分辨能力越低的被试,两个参数变化时其分辨能力提高的幅度就越大．揭示了视觉系统处理这种多刺激参量信息变化的能力和机制,对人类视觉系统在真实的视觉过程中如何处理朝向和对比度信息提供了认识．     

Effects of Prism Eyeglasses on Objective and Subjective Fixation Disparity

In optometry of binocular vision, the question may arise whether prisms should be included in eyeglasses to compensate an oculomotor and/or sensory imbalance between the two eyes. The corresponding measures of objective and subjective fixation disparity may be reduced by the prisms, or the adaptability of the binocular vergence system may diminish effects of the prisms over time. This study investigates effects of wearing prisms constantly for about 5 weeks in daily life. Two groups of 12 participants received eyeglasses with prisms having either a base-in direction or a base-out direction with an amount up to 8 prism diopters. Prisms were prescribed based on clinical fixation disparity test plates at 6 m. Two dependent variables were used: (1) subjective fixation disparity was indicated by a perceived offset of dichoptic nonius lines that were superimposed on the fusion stimuli and (2) objective fixation disparity was measured with a video based eye tracker relative to monocular calibration. Stimuli were presented at 6 m and included either central or more peripheral fusion stimuli. Repeated measurements were made without the prisms and with the prisms after about 5 weeks of wearing these prisms. Objective and subjective fixation disparity were correlated, but the type of fusion stimulus and the direction of the required prism may play a role. The prisms did not reduce the fixation disparity to zero, but induced significant changes in fixation disparity with large effect sizes. Participants receiving base-out prisms showed hypothesized effects, which were concurrent in both types of fixation disparity. In participants receiving base-in prisms, the individual effects of subjective and objective effects were negatively correlated: the larger the subjective (sensory) effect, the smaller the objective (motor) effect. This response pattern was related to the vergence adaptability, i.e. the individual fusional vergence reserves.     

Voluntarily controlled bi-stable slant perception of real and photographed surfaces

We have quantified voluntarily selected perceived slant of real trapezoidal surfaces (a 'reverse-perspective' scene) and their photographed counterparts (pictorial space). The surfaces were slanted about the vertical axis and observers estimated slant relative to the frontal plane. We were particularly interested in those cases in which binocular disparity and monocular perspective provided conflicting slant information. We varied the monocularly and binocularly specified surface slants independently across stimulus presentations. To eliminate texture and shading cues we used sand-blasted aluminium trapezoidal surfaces illuminated from all directions. When disparity-specified slant and perspective-specified slant were conflicting, observers were able to perceive the surfaces in two ways: they perceived either a trapezoid or a rectangle. Our main finding is twofold. First, when subjects chose to perceive the trapezoid, the slant estimates followed the disparity-predicted slant with only a slight underestimation, as if they selected a pure binocular representation of slant governed only by disparity. Second, when subjects chose to perceive the rectangle their estimates for real surfaces were similar to those for photographed surfaces, as if they selected a representation of slant governed by perspective foreshortening.     

Spatio-temporal parameters and the three-dimensionality of apparent motion: evidence for two types of processing

The minimum ISI required for perceiving apparent motion in depth was measured as a function of the 2D separation of stimuli and the physical separation of stimuli in depth. It was found that temporal thresholds increased as a function of the separation of stimuli in depth. This supports the results of previous research indicating that the perceived three-dimensionality of apparent motion in depth increases with ISI. In addition, the rate of threshold increase was significantly greater in displays with short 2D separations of stimuli than in displays with large 2D separations. This robust functional dissociation of thresholds indicates that the short-range system may be involved in the processing of apparent motion in depth in the former case.     

The Effects of Aging on Information-Processing Channels in the Sense of Touch: III. Differential Sensitivity to Changes in Stimulus Intensity

Detection thresholds and difference limens were measured for 16 subjects ranging from 19 to 91 years of age. The stimuli were 250-Hz bursts of vibration applied through a 3.0-cm² contactor to the thenar eminence of the right hand. Detection thresholds were higher in older than in younger subjects, as were the absolute values of difference limens. When the difference limen was expressed in relative terms as the proportion by which two stimuli had to differ in amplitude to be discriminated (δA/A), discriminative capacities were unaffected by aging except for stimuli slightly above the detection threshold, in which case the difference limens of older subjects were significantly higher than those of younger subjects. The results are consistent with the hypothesis that elevations in the detection thresholds of older subjects are the results of reduced afferent input to central brain centers that, with regard to their capacity to detect the presence of threshold-level stimuli and to discriminate differences among suprathreshold stimuli, are relatively unaffected by aging.     

Lateral sensitivity modulation explains the flanker effect in contrast discrimination

We used a dual-masking paradigm to study how contrast discrimination can be influenced by the presence of adjacent stimuli. The task of the observer was to detect a target superimposed on a pedestal in the presence of flankers. The flankers (i) reduce the target threshold at zero pedestal contrast, (ii) shift the target threshold versus pedestal contrast (TvC) function horizontally to the left on a log-log plot at high pedestal contrasts, and (iii) reduce the size of pedestal facilitation at low pedestal contrasts. The horizontal shift at high pedestal contrasts suggests that the flanker effect is a multiplicative factor that cannot be explained by previous models of contrast discrimination. We extend the divisive inhibition model of contrast discrimination by implementing the flanker effect as a lateral multiplicative sensitivity modulation. This extended model provides a good account of the data.     

Spatial pattern summation is phase-insensitive in the fovea but not in the periphery.

We measured the effect of phase coherence on the detectability of a chain of Gabor patches. The stimuli were elongated patterns consisting of 1-8 vertical Gabor patches, aligned vertically and either in phase or 180 deg out of phase from their immediate neighbors. In the fovea, the phase configuration had no effect on detection threshold, suggesting a full-wave rectification operation mediating foveal spatial summation. At 5 deg in the periphery, detection thresholds for the in-phase configuration were lower than those for the alternating-phase configuration, to an extent compatible with a half-wave rectification operation mediating peripheral spatial summation.     

Neural coding of 3D features of objects for hand action in the parietal cortex of the monkey.

In our previous studies of hand manipulation task-related neurons, we found many neurons of the parietal association cortex which responded to the sight of three-dimensional (3D) objects. Most of the task-related neurons in the AIP area (the lateral bank of the anterior intraparietal sulcus) were visually responsive and half of them responded to objects for manipulation. Most of these neurons were selective for the 3D features of the objects. More recently, we have found binocular visual neurons in the lateral bank of the caudal intraparietal sulcus (c-IPS area) that preferentially respond to a luminous bar or place at a particular orientation in space. We studied the responses of axis-orientation selective (AOS) neurons and surface-orientation selective (SOS) neurons in this area with stimuli presented on a 3D computer graphics display. The AOS neurons showed a stronger response to elongated stimuli and showed tuning to the orientation of the longitudinal axis. Many of them preferred a tilted stimulus in depth and appeared to be sensitive to orientation disparity and/or width disparity. The SOS neurons showed a stronger response to a flat than to an elongated stimulus and showed tuning to the 3D orientation of the surface. Their responses increased with the width or length of the stimulus. A considerable number of SOS neurons responded to a square in a random dot stereogram and were tuned to orientation in depth, suggesting their sensitivity to the gradient of disparity. We also found several SOS neurons that responded to a square with tilted or slanted contours, suggesting their sensitivity to orientation disparity and/or width disparity. Area c-IPS is likely to send visual signals of the 3D features of an object to area AIP for the visual guidance of hand actions.     

On visual orientation of dot patterns

Two-dimensional normally distributed random dot patterns were used in two experiments on visual orientation estimation. In the first experiment the patterns differed in their sample correlation and in dot number. In the second one the number of dots was maintained constant but the patterns were generated as a superposition of two normally distributed orthogonal sets composed of different number of dots. In both experiments the estimated orientation depended on stimuli correlation-with increasing correlation the estimated orientation gets closer to the orientation of the least square distance axis of the pattern. Even at very low unsignificant correlations there still remained a hint about stimulus orientation which was not estimated at random. Equalizing consecutively the number of dots in the two orthogonal dot patterns during the second experiment did not result in chance performance either. The bimodal angular distributions of the obtained responses permitted to approach the problem of orientation ambiguity. The results are discussed in terms of optimization processes taking place in the visual system.     

Methods for determining auditory evoked brain-stem response thresholds in human newborns

Previous investigators have reported that newborn auditory evoked brain-stem responses (ABRs) are 20–30 dB higher than adult psychophysical thresholds to the same stimuli. These investigators reduced the intensity of the stimulus until they no longer reported an ABR to the stimulus. We adapted 2 widely used psychophysical methods, the up-down-transformed response (UDTR) method and the method of constant stimuli, for ABR threshold determination of human newborns. Response judgments were made blindly. ABR thresholds of healthy normal newborns by both procedures were no more than 10–15 dB higher than adult psychophysical thresholds. The differences between the newborn ABR thresholds we reported and those in the literature were probably explained by different procedures including the method used to estimate adult psychophysical thresholds. The correlations between ABR thresholds and suprathreshold ABR latencies and amplitudes and latency and amplitude/intensity functions were modest at best. In normal newborns suprathreshold ABR measurements are of little value in predicting ABR thresholds.     

Differences in the sensations of warmth on the anterior torso of normal and spinal-cord transected individuals

The threshold to warming was measured at 10 sites on the anterior torso between the umbilicus and the clavicle of normal and spinal-cord transected individuals. In normal individuals, thresholds were higher on the thorax than on the abdomen. Men had higher and more variable thresholds than women. Magnitude estimations of supra-threshold stimuli showed that men offer verbal estimates of warmth that are about half of the size of the estimates given by women to the same stimuli. The psychometric function shows that in women, the sensation of warmth grows more rapidly than in men after starting from a higher initial value. After spinal-cord injury, thresholds for detection of warming were elevated. This effect was most noticeable within 8 cm of the anesthetic zone, but farther away, thresholds were still elevated but uniform as a function of distance, being about 30% higher than in normal individuals. After spinal-cord injury, the psychometric functions show that small stimuli elicit relatively large sensations and that these sensations grow more slowly with increasing skin temperatures than for normal individuals. Thus, for small warm stimuli spinal-cord-injured patients (both men and women) have a response similar to normal women but the slope of the psychometric function is flat, being similar to the slope observed for normal men.     

正常和卡那霉素中毒豚鼠听觉脑干诱发反应及频率跟随反应的比较研究

通过测定阈值和频谱分析,比较了正常和卡那霉素中毒后豚鼠听觉脑干反应(ABR)及频率跟随反应(FFR)的特性.正常FFR的非线性随刺激频率的减低而增加,表现为高次谐波的出现.从频谱中基频成分的峰很容易识别FFR阈值.卡那霉素作用后,高频FFR首先受到影响,波幅下降,阈值显著升高.低频FFR受到影响较小.同一动物ABR阈值尚未变化时高频FFR的基频峰值已下降,乃至消失.实验结果表明FFR对耳毒性药物中毒反应由于其包含有频率特性比ABR更灵敏,更便于定量分析.