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PubMed1996

The spatial grain of motion perception in human peripheral vision.

Motion reversal effects (the apparent reversal of the direction of motion of a high frequency sinusoidal grating) have been attributed to aliasing by the cone mosaic [Coletta et al. (1990). Vision Research, 30, 1631-1648] and postreceptoral layers [Anderson & Hess (1990). Vision Research, 30, 1507-1515] in human observers. We present data and a new model which suggest that at least two sampling arrays of different densities affect direction discrimination out to 30 degrees eccentricity. The first sampling layer matches anatomical estimates of the cone density. The second sampling layer is too dense to be the parasol cells alone; midget ganglion cells certainly contribute to this task. This is further evidence that motion perception is not mediated exclusively by the magnocellular stream.

Discrimination, Psychological↗
PubMed2000

Changes in horizontal oculomotor behaviour coincide with a shift in visual motion perception.

During full-field rotation of the visual field, subjects commonly experience an initial perception of object-motion which 'switches' to a perception of self-motion. We studied the characteristics of the horizontal optokinetic nystagmus responses evoked by a moving visual stimulus in these two perceptual states over a range of stimulus velocities. During self-motion perception mean eye position was found to shift more in the direction of the newly appearing stimulus elements with a slight reduction in slow phase gain in comparison to the nystagmus evoked during object-motion perception. The results may reflect a modified strategy of spatial attention with increased emphasis on anticipatory eye movements during visually induced self-motion perception.

Adult↗
PubMed1991

Motion perception in the peripheral visual field.

Thresholds were determined for the perception of the motion of a single bar moving at different positions in the field of view. Performance in the temporal hemified was slightly superior to that in the nasal hemifield and depended on the orientation as well as on the direction of the motion. The perception of horizontal motion was better than that of vertical motion. In spite of large variations, centrifugal motion was significantly more readily perceived than centripetal motion.

Humans↗
PubMed1998

Chronic motion perception deficits from midline cerebellar lesions in human.

A selective motion perception deficit is seen in patients with acute midline cerebellar lesions. Patients with more lateralized acute cerebellar damage do not demonstrate such a deficit (Nawrot M, Rizzo M. Vis Res 1995;35:723-731). However, as these patients were tested only between 10 and 14 days post-ictus, the stability of this perceptual deficit into the chronic phase remained undetermined. The current study extends the previous findings by showing that the motion perception deficit caused by mid-line cerebellar lesions remains permanent at least 2 years into the chronic phase. The extent and longevity of this deficit resembles that of the well known motion-blind patient LM who has a large cerebellar lesion in addition to her extensive cortical damage. Again, we propose that the mid-line cerebellar damage may produce a severe motion perception deficit by disruption the visual-motor integration mechanisms involved in perceptual stabilization, even though cortical motion processing mechanisms are unaffected.

Cerebellum↗
PubMed2002

The neural substrates of biological motion perception: an fMRI study.

We used fMRI to identify the brain areas related to the perception of biological motion (4 T EPI; whole brain). In experiment 1, 10 subjects viewed biological motion (a human figure jumping up and down, composed of 21 dots), alternating with a control stimulus created by applying autoregressive models to the biological motion stimulus (such that the dots' speeds and amplitudes were preserved whereas their linking structure was not). The lengths of the stimulus bouts varied, and therefore the transitions between biological motion and control stimuli were unpredictable. Subjects had to indicate with a button press when each transition occurred. In a related biological motion task, subjects detected short (1 s) disturbances within these displays. We also examined the neural substrates of motion and shape perception, as well as motor imagery, to determine whether or not the cortical regions involved in these processes are also recruited during biological motion perception. Subjects viewed linear motion displays alternating with static dots and a series of common objects alternating with band-limited white noise patterns. Subjects also generated imagery of their own arm movements alternating with visual imagery of common objects. Biological motion specific BOLD signal was found within regions of the lingual gyrus at the cuneus border, showing little overlap with object recognition, linear motion or motion imagery areas. The lingual gyrus activation was replicated in a second experiment that also mapped retinotopic visual areas in three subjects. The results suggest that a region of the lingual gyrus within VP is involved in higher-order processing of motion information.

Adult↗
PubMed1988

Drift-balanced random stimuli: a general basis for studying non-Fourier motion perception.

To some degree, all current models of visual motion-perception mechanisms depend on the power of the visual signal in various spatiotemporal-frequency bands. Here we show how to construct counterexamples: visual stimuli that are consistently perceived as obviously moving in a fixed direction yet for which Fourier-domain power analysis yields no systematic motion components in any given direction. We provide a general theoretical framework for investigating non-Fourier motion-perception mechanisms; central are the concepts of drift-balanced and microbalanced random stimuli. A random stimulus S is drift balanced if its expected power in the frequency domain is symmetric with respect to temporal frequency, that is, if the expected power in S of every drifting sinusoidal component is equal to the expected power of the sinusoid of the same spatial frequency, drifting at the same rate in the opposite direction. Additionally, S is microbalanced if the result WS of windowing S by any space-time-separable function W is drift balanced. We prove that (i) any space-time-separable random (or nonrandom) stimulus is microbalanced; (ii) any linear combination of pairwise independent microbalanced (respectively, drift-balanced) random stimuli is microbalanced and drift balanced if the expectation of each component is uniformly zero; (iii) the convolution of independent microbalanced and drift-balanced random stimuli is microbalanced and drift balanced; (iv) the product of independent microbalanced random stimuli is microbalanced; and (v) the expected response of any Reichardt detector to any microbalanced random stimulus is zero at every instant in time. Examples are provided of classes of microbalanced random stimuli that display consistent and compelling motion in one direction. All the results and examples from the domain of motion perception are transposable to the space-domain problem of detecting orientation in a texture pattern.

Fourier Analysis↗
PubMed2000

Self-motion perception during a sequence of whole-body rotations in darkeness.

The main aim of this study was to examine how postrotatory effects, induced by passive whole-body rotations in darkness, could alter the perception of motion and eye movements during a subsequent rotation. Perception of angle magnitude was assessed in a reproduction task: blindfolded subjects were first submitted to a passive rotation about the earth-vertical axis on a mobile robot. They were then asked to reproduce this angle by controlling the robot with a joystick. Stimulus rotations ranged from 80 degrees to 340 degrees. Subjects were given one of two delay instructions: after the stimulus, they either had to await the end of postrotatory sensations before starting reproduction (condition free delay, FD), or they had to start immediately after the end of the stimulus rotation (no delay, ND). The delay in FD was used as an incidental measure of the subjective duration of these sensations. Eye movements were recorded with an infrared measuring system (IRIS). Results showed that in both conditions subjects accurately reproduced rotation angles, though they did not reproduce the stimulus dynamics. Peak velocities reached in ND were higher than in FD. This difference suggests that postrotatory effects induced a bias in the perception of angular velocity in the ND condition.

Acceleration↗
PubMed1999

Motion perception over long interstimulus intervals.

Recent studies using moving arrays of textured micropatterns have suggested that motion perception can be supported by two mechanisms, one quasilinear and sensitive to the motion of luminance-defined local texture, the other nonlinear and coding motion of contrast-defined envelopes of texture (Baker & Hess, 1998; Boulton & Baker, 1993b). Here we used similar patterns to study motion perception under conditions previously shown to isolate the nonlinear mechanism (low micropattern densities and positive interstimulus intervals [ISIs]. We measured direction discrimination for two-flash apparent motion over a much larger range of ISIs, and susceptibility to masking by incoherently moving "distractor" micropatterns. The results suggest that two nonlinear mechanisms can support motion perception under these conditions. One operates only for relatively short ISIs (less than c. 100 msec), is sensitive to small spatial displacements, and is relatively insensitive to distractor masking. The other operates over much longer ISIs, is insensitive to small spatial displacements, and is highly disrupted by distractor masking. These results are in line with previous studies suggesting that three mechanisms support motion perception.

Attention↗
PubMedDate not supplied

Motion perception tested with reversing grating in Duane's syndrome.

Many papers have reported that motion perception asymmetry (MPA) is replaced by motion perception symmetry (MPS) by the 4th to 5th month after birth, when stereopsis starts to occur in normal infants. Duane's syndrome is a congenital motor abnormality, it does, however, reportedly show good stereopsis. We confirmed the stereopsis in Duane's syndrome and checked the motion perception (MP) by using the Reversing Grating Test to investigate if the congenital motor abnormality affects the MP in patients whose binocular sensory system is well developed. Thirty-eight Duane's syndrome patients aged 3 to 45 years were included in the present study. They were divided into 24 cases of Duane I, 9 cases of Duane II, 5 cases of Duane III. The Titmus Stereo Tests, Lang Stereotest, and TV-Random Dot Stereo Test were used to examine the stereopsis. Thirty-four patients had good stereopsis, and 4 had poor stereopsis. None of them showed MPA in any spatial frequencies (1/ 4, 1/2, 1 cycles/degree) examined. The Reversing Grating Test is useful for examining MPA in strabismus patients with eye movement limitations.

Adolescent↗
PubMed1994

Contribution of colour to the motion aftereffect and motion perception.

The aim in this work was to assess the contribution which colour information makes to the perception of motion. Two dependent variables were measured: the reaction time to a sudden cessation of motion (motion-end RT) and the duration of the motion aftereffect (MAE). In each case, a baseline measure of performance was made with the aid of a monochrome stimulus with a given contrast and added luminance noise. This was compared with performance when red/green colour modulation was added to the luminance display. Any difference between these measures would reveal the extent of chromatic input. For motion-end RT the addition of colour had little effect under conditions where the stimulus had a strong luminance component and little added luminance noise. Increasing departures from these conditions revealed the contribution of a colour-sensitive mechanism. In general, the chromatic contribution to MAE duration was much smaller than was the equivalent contribution to motion-end RT, thus possibly indicating a neurological dissociation between the mechanisms subserving these effects. The results of an experiment in which the effect of different temporal frequencies of the added luminance noise was assessed supported this dissociation between MAE and motion-end RT. The findings are therefore consistent with there being two motion (sub)systems, which differ in the extent of chromatic input. The subsystem revealed by MAE measures is less affected by colour information.

Color Perception↗
PubMed1993

The characteristics of residual motion perception in the hemifield contralateral to lateral occipital lesions in humans.

Unilateral damage to the lateral occipital region in humans can give rise to impaired motion perception in the contralateral visual field [Plant et al. (1993), Brain, 116, 1303-1335]. We report the following characteristics of the residual vision. (i) Spatial acuity and spatial frequency discrimination are not affected. (ii) Contrast thresholds for direction-of-motion (DOM) discrimination of luminance modulated (LMod) sine-wave gratings is unaffected regardless of drift temporal frequency and the effect of spatial and temporal frequency on drifting/counterphase sensitivity ratios is normal (providing further evidence that cortical directionally selective mechanisms are intact). (iii) Contrast thresholds for DOM discrimination of contrast modulated (CMod) gratings are elevated by a log unit across a range of drift velocities. (iv) The residual motion perception shows neither a directional nor a naso-temporal asymmetry. (v) Weber fractions for velocity discrimination are shown in one patient in whom this measurement was carried out, to be elevated by around a factor of three but the functions relating velocity discrimination to stimulus contrast and to the velocity of the standard are parallel in the affected and unaffected hemifields. (vi) Weber fractions for temporal frequency discrimination using counterphase modulated gratings are also elevated. We conclude that the degraded motion perception is mediated by mechanisms which have similar contrast and temporal properties to those subserving normal motion perception. Mechanisms subserving DOM discrimination of LMod gratings may be spared because they are more widely distributed in extra-striate cortex than mechanisms subserving non-Fourier (second-order) motion perception or velocity discrimination. The anomaly resembles that described in some recent animal studies of impaired motion perception after extra-striate cortical damage.

Adult↗
PubMed1991

Reversed rotary motion perception.

A stroboscopically presented revolving annulus composed of dots is used to elicit rotary motion perception. Observers judge the direction of rotary motion. We find sharp and gradual transitions in the probability for reversed motion perception as a function of the angle of rotation between successive frames. These transitions reveal that matches between nonsuccessive frames can dominate motion perception. The transitions are scale invariant. The strength of a match is discussed in terms of a motion strength function, which is a separable function of the angle of rotation between successive frames and the frame repetition rate. The dependence of motion strength on the frame repetition rate (time function) is computed from the transitions. The similarity of this time function for rotary motion with the time function for linear motion [Psychol. Rev. 88, 171 (1981)] suggests that mechanisms for the discrimination of rotary motion address local detectors of linear motion.

Humans↗
PubMed2002

Neural correlates of visual-motion perception as object- or self-motion.

Both self-motion and objects moving in our visual field generate visual motion by displacing images on the retina. Resolving this ambiguity may seem effortless but large-field visual-motion stimuli can yield perceptual rivalry between the real percept of object-motion and the illusory percept of self-motion (vection). We used functional magnetic resonance imaging to record brain activity in human observers exposed to constant-velocity roll-motion. This stimulus induced responses in areas reaching from calcarine to parieto-occipital and to ventral and lateral temporo-occipital cortex and the anterior insula. During vection, early motion-sensitive visual areas and vestibular parieto-insular cortex deactivated, whereas higher-order parieto- and temporo-occipital areas known to respond to optical flow retained identical activity levels. Within this sustained response, these latter areas displayed transient activations in response to each perceptual switch as identified in event-related analyses. Our results thus show that these areas are responsive to the type of visual motion stimulus and highly sensitive to its perceptual bistability. The only region to be more active during perceived self-motion was in, or close to, the cerebellar nodulus. This activation may correspond to the gain increase of torsional optokinetic nystagmus during vection and/or to changes in sensory processing related to the rotational percept. In conclusion, we identified neural correlates of perceiving self-motion from vision alone, i.e., in the absence of confirmatory vestibular or proprioceptive input. These functional properties preserve the organism's ability to move accurately in its environment by relying on visual cues under conditions when the other spatial senses fail to provide such information.

Adult↗
PubMed2001

A psychophysical measurement and analysis of motion perception in normal and binocularly deprived monkeys.

PURPOSE: To measure psychophysically the thresholds for motion detection in the nasal and temporal directions under monocular viewing conditions in monkeys reared under conditions of daily alternating monocular occlusion (AMO). The hypothesis was that motion perception would be asymmetric with more sensitivity for motion in the nasal direction. METHODS: Three monkeys subjected to AMO (AMO monkeys) and three normal monkeys were studied. All were trained with operant conditioning techniques to discriminate coherent from random motion in a random dot display. The percentage of dots in the display that moved either left or right was varied. Thresholds for motion detection of nasally directed and temporally directed stimuli were measured to determine whether the motion perception of AMO monkeys was asymmetric, as predicted. RESULTS: A two-factor analysis of variance revealed a statistically significant difference between treatment groups (normal versus AMO) and directions (nasal versus temporal) and a significant interaction. The interaction was due to a significant difference between nasal and temporal directions for the AMO group, but no significant difference for the normal group. Planned comparisons were performed based on each animal's best eye (eye most sensitive to nasal motion) and worst eye (eye least sensitive to temporal motion). No significant differences were found between the two groups in the best eyes' responses to the nasal direction, but the worst eyes' responses in the temporal direction were significantly poorer in the AMO group. A neural model that can account for these findings is based on a Hebbian teacher located in the nucleus of the optic tract that strengthens connections of a subpopulation of directionally selective cortical neurons. CONCLUSIONS: AMO rearing results in asymmetric motion perception. Thresholds for detecting nasally directed motion are normal, whereas thresholds for detecting temporally directed motion are deficient. These results demonstrate that motion-processing mechanisms in primates exhibit experience-dependent developmental neural plasticity. The locus of the neural plasticity could be a subpopulation of directionally selective neurons in the striate cortex (V1).

Animals↗
PubMed1990

On and off pathway contributions to apparent motion perception.

We studied the separability and/or interaction of the On and Off pathways in their role as inputs to visual motion perception. Using the long-range motion perception system, we asked if the motion system can use brightness polarity information, by testing whether correspondence is preferred between elements for which brightness polarity is preserved. We found such a preference, suggesting that brightness polarity information is indeed available to the motion system. However, under certain conditions motion is perceived even though the brightness polarity of apparent motion stimulus elements is reversed, indicating that the apparent motion system does integrate information from these two pathways. The source of the preference for maintaining polarity seems not to be the different brightnesses of the dark and bright stimulus elements, but the very fact that information must be integrated from different pathways. We relate the characteristics of the dependence of the motion perception on element contrast and contrast sign to those of previously reported visual evoked potential responses to brightness increments and decrements.

Contrast Sensitivity↗
PubMed2001

[Change of cone's motion perception in patients with primary open angle glaucoma].

OBJECTIVE: To assess the change of cone's motion perception in primary open angle glaucoma (POAG). METHODS: Equi-luminance random dots moving test was used to determine the change of motion perception of blue, green and red cones in 51 eyes with POAG. To isolate the three kinds of cones, the blue, green and red visual targets were displayed on the yellow, purple and blue-green background respectively. RESULTS: The direction discrimination thresholds of motion perception from blue, green and red cones were all damaged in POAG compared to that of the normal group, and among them the blue cone was the most obviously damaged. CONCLUSIONS: These findings indicate that cone's motion perception, especially the blue cone's, may reveal pre-clinical visual nerve damage in POAG.

Adolescent↗
PubMed1987

Object-motion detection affected by concurrent self-motion perception: applied aspects for vehicle guidance.

Thresholds and response times for object-motion detection are significantly raised during concurrent real or visually induced self-motion perception. This was demonstrated by standardized laboratory experiments in which subjects had to react to a suprathreshold visual stimulus (1 degree-light spot moving with 5 degrees/s speed) under different stimulus conditions of simultaneously perceived self-motion. Elevated response times (mean elevation factor: 3.27) were also obtained for the detection of changes in inter-vehicle distance (headway) under real road conditions with the simultaneous involvement of self- and object-motion perception compared to a corresponding (object-motion perception) simulation in the laboratory without any self-motion. With regard to vehicle guidance, existing concepts of safe stopping distances, which depend upon adequate detection of a collision course and the corresponding reaction times, have to be recalculated.

Adult↗
PubMed1975

The Aubert-Fleischl phenomenon: a temporal frequency effect on perceived velocity in afferent motion perception.

Apparent velocities of moving visual stimuli are known to be different depending on whether the subject pursues the stimulus (efferently controlled motion perception) or whether the eye is stationary and the image moves across the retina (afferent motion perception). Afferent motion perception of a periodic pattern or a moving single object causes overestimation of velocity (magnitude estimations) as compared to smooth pursuit. This socalled Aubert-Fleischl phenomenon is shown to depend on local temporal frequency stimulation on the retina caused by the repetitive passage of contrast borders of the moving periodic pattern. This is evidenced by the fact that for a given stimulus speed the amount of overestimation is a function of the spatial frequency of the pattern (or the angular subtend of a single moving object) and that the Aubert-Fleischl phenomenon is not observed if a single edge moves. Background characteristics seem not to influence the apparent velocity during smooth pursuit.

Adult↗