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Intrasaccadic perception.

Mammalian vision has a lowpass frequency characteristic that filters out fast temporal oscillations. Thus, fast-drifting gratings cannot be detected with static eyes, but the same gratings can easily be detected by executing saccades. Because these gratings are invisible under fixation, they are useful for isolating and studying intrasaccadic perception, which is normally masked by presaccadic and postsaccadic perception. We have conducted a number of psychophysical studies using these stimuli, and here we report that intrasaccadic visual processing allows for motion perception, that gratings drifting in the direction of a saccade are perceived as having more contrast than the same gratings drifting in the opposite direction, and that intrasaccadic contrast perception has sufficient grain to allow psychophysical matching of the perceived contrast of gratings drifting in opposite directions. The conditions in which these phenomena occur disprove a recent hypothesis that intrasaccadic motion perception occurs for stimuli processed by the magnocellular system, and our results can be explained by assuming that the temporal lowpass characteristic that accounts for flicker fusion phenomena under vision with static eyes is also operative during saccades.

Contrast Sensitivity↗

Perception of biological motion.

Boundary conditions for perception of biological motion were explored with the use of computer-generated point-light animation sequences. Perception of this unique form of structure from motion is immune to variations in dot contrast polarity, dot disparity, and spatial-frequency filtering. Biological motion is perceived in texture-defined animation sequences that presumably stimulate only second-order motion pathways, and it is undisturbed by dichoptic presentation of portions of the animation tokens separately to the two eyes.

Computer Graphics↗

Is experimental motion blindness due to sensory suppression? An ERP approach.

Recent psychophysical studies have revealed attentional modulation of visual motion perception and interest now focuses on the locus of this interaction. Using event-related brain potentials (ERPs) we examined whether transient motion blindness evoked in a dual task [Vision Res. 41 (2001) 1613-1617] is related to a selection process occurring at the stage of sensory processing or at a higher level. In our paradigm, a particular change of colour of the fixation point cued the subject to detect a brief episode of coherent random dot motion embedded in a succession of episodes of incoherent motion. Detection of the coherent motion was significantly impaired when it occurred simultaneously with the colour cue, and recovered over the subsequent 300 ms. This functional relationship was reflected in the amplitude of a sensory, motion-evoked component (N200), and in a late positive complex (P300). However, a direct comparison of ERPs produced by stimuli that were detected or missed revealed differences only in the P300 component. These results indicate that attenuation of sensory motion processing does not account for this transient, attention-induced deficit in visual motion perception.

Adult↗

Encoding of three-dimensional structure-from-motion by primate area MT neurons.

We see the world as three-dimensional, but because the retinal image is flat, we must derive the third dimension, depth, from two-dimensional cues. Image movement provides one of the most potent cues for depth. For example, the shadow of a contorted wire appears flat when the wire is stationary, but rotating the wire causes motion in the shadow, which suddenly appears three-dimensional. The neural mechanism of this effect, known as 'structure-from-motion', has not been discovered. Here we study cortical area MT, a primate region that is involved in visual motion perception. Two rhesus monkeys were trained to fixate their gaze while viewing two-dimensional projections of transparent, revolving cylinders. These stimuli appear to be three-dimensional, but the surface order perceived (front as opposed to back) tends to reverse spontaneously. These reversals occur because the stimulus does not specify which surface is in front or at the back. Monkeys reported which surface order they perceived after viewing the stimulus. In many of the neurons tested, there was a reproducible change in activity that coincided with reversals of the perceived surface order, even though the stimulus remained identical. This suggests that area MT has a basic role in structure-from-motion perception.

Animals↗

Attending to visual or auditory motion affects perception within and across modalities: an event-related potential study.

The present event-related potential (ERP) study examined the role of dynamic features in multisensory binding. It was tested whether endogenous attention to the direction of motion affects processing of visual and auditory stimuli within and across modalities. Human participants perceived horizontally moving dot patterns and sounds that were presented either continuously (standards) or briefly interrupted (infrequent deviants). Their task was to detect deviants moving in a particular direction within a primary modality, but to detect all deviants irrespective of their motion direction within the secondary modality. Attending to the direction of visual motion resulted in a broad selection negativity (SN) starting at about 200 ms post-stimulus onset, and attending to the direction of auditory motion resulted in a positive difference wave at 150 ms that was followed by a broad negativity starting at about 200 ms (unimodal effects). Moreover, dot patterns moving in a direction that was attended within audition were detected faster and more accurately than oppositely moving stimuli and elicited a cross-modal SN wave. Corresponding cross-modal behavioural and ERP results were obtained for sounds moving in a direction that was attended within vision. Unimodal and cross-modal ERP attention effects partially differed in their scalp topography. The present study shows that dynamic features (direction of motion) may be used to link input across modalities and demonstrates for the first time that these multisensory interactions take place as early as about 200 ms after stimulus onset.

Acoustic Stimulation↗

Mechanism of neurophysiological treatment of amblyopia using functional magnetic resonance imaging.

PURPOSE: To research the mechanism of neurophysiological treatment of amblyopia by observing the visual cortex activation under rotating grating stimulus with functional magnetic resonance imaging (MRI), and identify the components of the activation. METHODS: Nine healthy volunteers were examined using gradient-recalled echo and echo-planar imaging (GRE-EPI) pulse sequence performed at the 1.5 Tesla MRI scanner. In the block designing, rotating grating, stationary grating and luminance were plotted as task states, stationary grating, luminance and darkness as control states, respectively. The tasks of stimuli included 6 steps. Imaging processing and statistical analysis were carried out off-line using statistical parametric mapping (SPM99) software in single-subject. RESULTS: Some individual areas of visual cortex were activated by various stimuli information supplied by rotating grating. The strong activation in the middle of occipital lobe related to the stimuli of luminance, bilateral activation of Brodmann's 19th area related to visual motion perception, and the mild activation in the middle of occipital lobe related to form perception. CONCLUSION: The plotting of control state is important in bock design. The effective visual information of rotating grating includes components of luminance, visual motion perception and form perception. Functional MRI has potential as a tool for studying the physiological mechanism of visual cortex.

Adult↗

Anisotropy in judging the absolute direction of motion.

The angular dependence of precision measurements is well established as the oblique effect in motion perception. Recently, it has been shown that the visual system also exhibits anisotropic behaviour with respect to accuracy of the absolute direction of motion of random dot fields. This study aimed to investigate whether this angular dependent, directional bias is a general phenomenon of motion perception. Our results demonstrate, for single translating tilted lines viewed foveally, an extraordinary illusion with perceptual deviations of up to 35 degrees from veridical. Not only is the magnitude of these deviations substantially larger than that for random dots, but the general pattern of the illusion is also different from that found for dot fields. Significant differences in the bias, as a function of line tilt and line length, suggest that the illusion does not result from fixed inaccuracies of the visual system in the computation of direction of motion. Potential sources for these large biases are motion integration mechanisms. These were also found to be anisotropic. The anisotropic nature and the surprisingly large magnitude of the effect make it a necessary consideration in analyses of motion experiments and in modelling studies.

Anisotropy↗

Sensitivity to colour- and to orientation-carried motion respectively improves and deteriorates under equiluminant background conditions.

This study presents two distinct effects produced by manipulation of the background illumination on the directional sensitivity to colour- and orientation-carried motion. The two motion percepts were produced with two of a class of stimuli extensively used by the first and last authors in apparent-motion studies. The stimuli were designed to produce motion perception by virtue of spatiotemporal matching of (a) colour with orientation systematically mismatched (Colour across Orientation, CxO) and of (b) orientation with colour systematically mismatched (OxC). An increase in background illumination from dark to the equiluminance point (relative to the luminance of the discrete stimulus microelements) entails a significant increase and decrease of directional performances with CxO and OxC stimuli, respectively. It is proposed that these anti-symmetrical background effects have distinct neurophysiological origins. For CxO stimuli, improvement of directional performances at the equiluminant point is presumably due to the inactivation of the inhibitory effect of the luminance-motion pathway on the chromatic-motion pathway. The opposite effect obtained with OxC stimuli, previously referred to as the veto effect (Gorea and Papathomas, 1988 Invest. Ophthal. Vis. Sci. Suppl., 29, 265), is supposed to be entailed by the inactivation of the luminance-oriented mechanism, the only motion sensitive mechanism activated by this stimulus configuration.

Color Perception↗

When texture takes precedence over motion in depth perception.

Both texture and motion can be strong cues to depth, and estimating slant from texture cues can be considered analogous to calculating slant from motion parallax (Malik and Rosenholtz 1994, report UCB/CSD 93/775, University of California, Berkeley, CA). A series of experiments was conducted to determine the relative weight of texture and motion cues in the perception of planar-surface slant when both texture and motion convey similar information. Stimuli were monocularly viewed images of planar surfaces slanted in depth, defined by texture and motion information that could be varied independently. Slant discrimination biases and thresholds were measured by a method of single-stimuli binary-choice procedure. When the motion and texture cues depicted surfaces of identical slants, it was found that the depth-from-motion information neither reduced slant discrimination thresholds, nor altered slant discrimination bias, compared to texture cues presented alone. When there was a difference in the slant depicted by motion and by texture, perceived slant was determined almost entirely by the texture cue. The regularity of the texture pattern did not affect this weighting. Results are discussed in terms of models of cue combination and previous results with different types of texture and motion information.

Analysis of Variance↗

Akinetopsia from nefazodone toxicity.

PURPOSE: To investigate two cases of selective impairment of motion perception (akinetopsia) induced by toxicity from the antidepressant nefazodone, a new drug that blocks serotonin reuptake and antagonizes 5-HT2 receptors. METHODS: Case reports. RESULTS: A 47-year-old man receiving nefazodone (Serzone; Bristol-Meyers Squibb, New York, N.Y.) (100 mg twice daily), reported a bizarre derangement of motion perception. Moving objects were followed by a trail of multiple "freeze-frame" images, which dissipated promptly when motion ceased. A 48-year-old woman receiving nefazodone (400 mg daily at bedtime) reported a similar phenomenon, with visual trails following moving objects. In both patients, vision returned to normal after the dosage of nefazodone was reduced or eliminated. CONCLUSIONS: Nefazodone toxicity can result in akinetopsia, characterized by the inability to perceive motion in a normal, smooth fashion; persistence of multiple, strobelike images; and visual trails behind moving objects. In this rare syndrome, stationary elements are perceived normally, indicating that nefazodone causes selective impairment of pathways involved in motion processing in the visual system.

Antidepressive Agents, Second-Generation↗

Absence of a common functional denominator of visual disturbances in cerebellar disease.

Several studies have demonstrated disturbances of visual perception in patients suffering from cerebellar disease. In an attempt to determine the cause of these visual disturbances and thereby the cerebellar contribution to vision, we designed two sets of experiments in which we tested (i) the possibility of a general magnocellular deficit in cerebellar disease and (ii) the alternative possibility of impaired spatial attention underlying visual disturbances in cerebellar patients. The first set of experiments consisted of a test of position discrimination, a parvocellular function and tests tapping different aspects of motion perception including speed discrimination, direction discrimination and the ability to extract a coherent motion signal embedded in noise. The second set of experiments compared the performance on two different classes of texture discrimination. The first one required fast and precise shifts of focal spatial attention ('serial search'), the second one, testing preattentive texture discrimination ('pop-out'), did not. In the first set of experiments cerebellar patients were impaired on the position discrimination task as well as several, albeit not all, tests of motion perception. The pattern of disturbances obtained was neither compatible with the notion of a selective magnocellular deficit nor the idea, originally put forward by Ivry and Diener (J Cogn Neurosci 1991; 3: 355-66) that visual deficits are secondary to an impaired measurement of time. In the second set of experiments, cerebellar patients showed normal performance on pop-out tasks and normal performance on all variants of the serial search task except for the one requiring comparison of a single element presented with a sample of the target in short-term memory. In summary, our results support the existence of visual disturbances in cerebellar disease, but provide evidence against a common, simple denominator such as a timing deficit, deficient cerebellar modulation of magnocellular circuitry, deficits of spatial attention or visual working memory.

Adult↗

M.I.T./Canadian vestibular experiments on the Spacelab-1 mission: 6. Vestibular reactions to lateral acceleration following ten days of weightlessness.

Tests of otolith function were performed pre-flight and post-flight on the science crew of the first Spacelab Mission with a rail-mounted linear acceleration sled. Four tests were performed using horizontal lateral (y-axis) acceleration: perception of linear motion, a closed loop nulling task, dynamic ocular torsion, and lateral eye deviations. The motion perception test measured the time to detect the onset and direction of near threshold accelerations. Post-flight measures of threshold and velocity constant obtained during the days immediately following the mission showed no consistent pattern of change among the four crewmen compared to their pre-flight baseline other than an increased variability of response. In the closed loop nulling task, crewmen controlled the motion of the sled and attempted to null a computer-generated random disturbance motion. When performed in the light, no difference in ability was noted between pre-flight and post-flight. In the dark, however, two of the four crewmen exhibited somewhat enhanced performance post-flight. Dynamic ocular torsion was measured in response to sinusoidal lateral acceleration which produces a gravitionertial stimulus equivalent to lateral head tilt without rotational movement of the head. Results available for two crewmen suggest a decreased amplitude of sinusoidal ocular torsion when measured on the day of landing (R+0) and an increasing amplitude when measured during the week following the mission.

Acceleration↗

The temporal characteristics of motion processing in hMT/V5+: combining fMRI and neuronavigated TMS.

Functional imaging has demonstrated the specific involvement of the human middle-temporal complex (hMT/V5+) during processing of moving stimuli. Some studies applied transcranial magnetic stimulation (TMS) to investigate the causal relevance of hMT/V5+ for motion perception. Although the studies used similar visual stimuli and TMS parameters, the critical time point of functionally relevant hMT/V5+ activity differed by 100 ms and more. The present study aimed to elucidate further the temporal characteristics of motion processing in hMT/V5+ by investigating all critical time windows currently debated in the literature. In contrast to previous studies, we used TMS neuronavigation based on individual fMRI results of five participants to target hMT/V5+, applying single-pulse TMS at 24 different time windows (-50 till +200 ms relative to stimulus onset). We revealed that TMS significantly impaired motion perception when applied over hMT/V5+ at 40 to 30 ms before as well as 130 to 150 ms after onset of the moving stimuli. While the late effective time window conforms to results from previous experiments, we did not find evidence for an early time window around 0 ms that has been reported in other studies. Our neuronavigation approach enabled us to quantify the interindividual variance in the exact location of hMT/V5+ and the respective TMS target position on the skull of the participants. Considering that shifting the TMS coil position only by a few millimeters can already lead to a complete loss of TMS effects, our study clearly demonstrates the utility of neuronavigated TMS when investigating specific neuronal effects as in the case of motion processing.

Adult↗

Perception of apparent motion across the retinal midline following commissurotomy.

One subject (L.B.) with complete forebrain commissurotomy, another (D.K.) with posterior callosotomy, and 12 normal controls, were shown either single lights, simultaneous pairs, or successive pairs, presented either within the left or right visual fields or bilaterally. Regardless of location, all subjects scored at or near ceiling in discriminating: (1) simultaneous pairs from single lights, (2) successive pairs from single lights, (3) simultaneous pairs from successive pairs, and (4) leftward succession from rightward succession. However, with bilateral presentation, L.B. was often slow to respond to successive lights, and his accuracy in detecting bilateral succession deteriorated when successive presentations were intermixed with simultaneous pairs and single lights. These and other results suggest that three mechanisms may contribute to the discrimination of apparent motion: the detection of simultaneous events, a subcortically mediated switch in attention from first to second location, and cortical tracking between locations. Cortical tracking across the midline is incapacitated following complete forebrain commissurotomy.

Adult↗

The perception of object motion during smooth pursuit eye movements: adjacency is not a factor contributing to the Filehne illusion.

During smooth pursuit eye movement performance often an illusory motion of background objects is perceived. This so called Filehne illusion has been quantified and explored by Mack and Herman [Q. J.exp. Psychol. 25, 71-84 (1973); Vision Res. 18, 55-62 (1978)]. According to them two independent factors contribute to the Filehne illusion: (1) a subject relative factor, viz. the underregistration of pursuit eye movements by the perceptual system, and (2) an object relative factor, viz. adjacency of the pursued fixation point and the background stimulus. The evidence of the present experiment supports the former but rejects the latter as a contributing factor. Instead of the concept of adjacency, an alternative theoretical extension of the subject relative factor is offered.

Adult↗

Contribution of transient and sustained responses to the perception of apparent motion.

The likelihood of seeing apparent motion (AM) was measured as a function of inter-stimulus-interval (ISI) between two isolated Gabor patches separated by 4 deg with spatial frequency (0.75, 2.0 and 4.5 c/deg) and exposure duration (33 and 1000 msec) as parameters. For the short stimuli, the likelihood of AM for the low-spatial-frequency of 0.75 c/deg was higher than that for the high-spatial-frequency of 4.5 c/deg, but for the long stimuli, the former was similar to, or lower than the latter. Decreasing the mean luminance from 190 to 0.8 cd/m2 impaired AM for the short stimuli of 2.0 c/deg, but improved AM for the long stimuli. The dependencies of AM on spatial frequency, exposure duration and adaptation level may be ascribed to the changing contribution of the transient and the sustained responses.

Adaptation, Ocular↗

Measurement of rate of expansion in the perception of radial motion.

Optic flow generated by rigid surface patches can be decomposed into a small number of elementary motion types. In these experiments, we show that the human visual system can evaluate expansion, one of these motion types, metrically. Moreover, we show that the discrimination of rates of expansion are spatially local. Because the estimation of the focus of expansion is somewhat imprecise, this locality sometimes produces predictable errors in the estimation of rate of expansion. One can make predictions like this with a model adapted from one previously developed for angular-velocity discrimination.

Discrimination, Psychological↗