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PubMed1997

Second-order motion perception in peripheral vision: limits of early filtering.

Spatial and temporal analysis of contrast-modulated sine-wave gratings reveals that the second-order motion stimulus contains two sidebands, with equal energy but moving in opposite directions, flanking a stationary carrier. Any early linear spatial filtering process in the visual system that attenuates one sideband more than the other will be detrimental to the balance between the two sidebands, so that the perceived direction of the carrier might be opposite to that of the envelope motion. We tested this hypothesis by using contrast-modulated gratings presented centrally or at 20 deg in the horizontal nasal field with a two-alternative forced-choice staircase paradigm. We found that when the envelope frequency was close to that of the carrier, a second-order stimulus whose envelope motion direction was correctly identified in the fovea appeared to drift in the opposite direction in the periphery. Further increasing the envelope spatial frequency resulted in a reversed motion percept in both central and peripheral viewing conditions. For subjects to identify correctly the direction of motion of the envelope, the spatial frequency ratio of the carrier to the envelope had to be more than 2 in the fovea and more than 6 in the periphery. These phenomena in second-order motion perception can be explained by a linear model of motion detection with an early spatial filtering process. Further experiments and computer simulation show that undersampling of the carrier has little effect on second-order motion perception in the periphery, as long as the carrier is detectable.

Adult↗
PubMed1995

The consequences of inactivating areas V1 and V5 on visual motion perception.

We studied the capacity of normal humans to discriminate the direction of motion of visual stimuli when areas V1 or V5 were reversibly inactivated with transcranial magnetic stimulation. We found that (i) magnetic stimulation of V5 at intervals of -20 to +10 ms before or after the onset of visual stimulation was effective in abolishing motion perception--other delays were not; (ii) magnetic stimulation of V1 abolished motion perception only marginally and at delays which were significantly different from those obtained with V5, the stimulation now being effective only at delays of 60-70 ms after the onset of visual stimulation. We conclude (i) that stimulation of V5 is a much more potent way of inducing akinetopsia (motion imperception) than stimulation of V1; (ii) that perceptually effective visual motion signals reach V5 at or before 30 ms and reach V1 at or before 60 ms--consequently, perceptually effective motion signals reach V5 before they reach V1; (iii) that, given the time course of arrival of signals in V1 and V5, it takes about 30-50 ms for signals from V1 to reach V5. We conclude further that there are probably two components reaching V5 from the retina, a fast one which bypasses V1 and a slow one which reaches it through V1.

Brain Mapping↗
PubMed1998

Anisotropies in visual motion perception: a fresh look.

We measured motion-detection and motion-discrimination performance for different directions of motion, using stochastic motion sequences. Random-dot cinematograms containing 200 dots in a circular aperture were used as stimuli in a two-interval forced-choice procedure. In the motion-detection experiment, observers judged which of two intervals contained weak coherent motion, the other internal containing random motion only. In the direction-discrimination experiment, observers viewed a standard direction of motion followed by comparison motion in a slightly different direction. Observers indicated whether the comparison was clockwise or counterclockwise, relative to the standard. Twelve directions of motion were tested in the detection task and five standard directions (three cardinal directions and two oblique directions) in the discrimination task. Detection thresholds were invariant with direction of motion, but direction-discrimination thresholds were significantly higher for motion in oblique directions, even at low-coherence levels. Results from control conditions ruled out monitor artifacts and indicate that the oblique effect is relative to retinal coordinates. These results have broad implications for computational and physiological models of motion perception.

Anisotropy↗
PubMed1997

Visually induced motion perception and visual control of postural sway in congenital nystagmus.

In congenital nystagmus (CN) the threshold for detecting motion of visual objects is increased. To determine whether this increase is due to a deterioration of visual motion signals or whether visual-vestibular interactions (which are necessary to judge object-motion in space) are also involved we examined how CN patients use visual motion signals to evaluate self-motion in perceptual and behavioral tasks. Using an optokinetic drum we measured the minimum optokinetic acceleration necessary to induced motion perception of the visual environment in CN patients. This threshold was significantly elevated in the CN patients compared with normals (20.1 deg/s2 to 3.25 deg/s2). We further addressed the question whether the elevation of this threshold is due to a deficiency in evaluating visual motion in general or to a specific modification affecting the percept of visual object-motion with respect to the inertial reference only. We thus measured the latency of visually induced self-motion perception, which was found to be very similar or even slightly smaller (1.7 +/- 0.7 s) compared with normals (2.2 +/- 1.7 s). Moreover, subjects with CN were found to use vision quite efficiently for the visual stabilization of posture (Romberg quotient 2.0 +/- 1.16), even if they did not reach the level of normals (Romberg quotient 3.7 +/- 1.1). The results indicate that CN affects the estimate of object-motion in a specific and much more severe way than the estimate of self-motion. The minimal effect of CN on self-motion perception can be explained by the low pass characteristics of the optokinetic input to self-motion perception. The specific deficiency in detecting object-motion indicates that adaptation to CN occurs on the level of visual--vestibular interactions for the perception of visual object-motion and not on the level of visual motion signals.

Adolescent↗
PubMed1996

Biases of motion perception revealed by reversing gratings in humans who had infantile-onset strabismus.

Motion perception was tested by requiring adult subjects to view gratings that remained stationary but reversed in contrast several times per second. Subjects viewed monocularly and judged whether the gratings were stationary, or moving in one direction, in successive 3s trials. Subjects who had early-onset strabismus most frequently perceived vertically oriented gratings to be moving nasalward, and horizontally oriented gratings to be moving up or down. Normal subjects and subjects who had late-onset strabismus most frequently perceived the gratings to be stationary. The asymmetries of motion perception in early-onset strabismus imply that the visual motion neurons of cerebral cortex develop properly only if they receive normal binocular input during infancy.

Adolescent↗
PubMed1994

Psychophysical evidence of differential latencies of colour inputs to motion perception.

A novel psychophysical observation allows the determination of the relative latencies with which long, middle, and short cone signals provide input to motion perception. It is known that when two spatially displaced isoluminant stimuli in spectrally different colours are simultaneously presented, any temporal lag between the perception of the two will, due to the spatial displacement, cause the perception of apparent motion. The illusion reported here occurs through the inadvertent production of spatial displacement; peripheral observation of the boundary between two differently-coloured neighbouring areas which alternately interchange colours leads, due to transverse chromatic aberration caused by the eye's optics, to the formation of a double boundary on the retina, the serial perceptions of which create the sensation of motion. By offsetting the relative temporal phases of any two colours we have determined the relative magnitude of the latencies with which they provide input to motion perception. In all subjects motion of blue is perceived after that of red, and green is perceived after that of blue. The origins of these latencies are unclear.

Color Perception↗
PubMed2000

Orientation specificity in biological motion perception.

We addressed the issue of how display orientation affects the perception of biological motion. In Experiment 1, spontaneous recognition of a point-light walker improved abruptly with image-plane display rotation from inverted to upright orientation. Within a range of orientations from 180 degrees to 90 degrees, it was dramatically impeded. Using ROC analysis, we showed (Experiments 2 and 3) that despite prior familiarization with a point-light figure at all orientations, its detectability within a mask decreased with a change in orientation from upright to a range of 90 degrees-180 degrees. In Experiment 4, a priming effect in biological motion was observed only if a prime corresponded to a range of deviations from upright orientation within which the display was spontaneously recognizable. The findings indicate that display orientation nonmonotonically affects the perception of biological motion. Moreover, top-down influence on the perception of biological motion is limited by display orientation.

Adolescent↗
PubMed1998

[A study of motion perception in primary open-angle glaucoma].

OBJECTIVE: To study the characteristics of the motion perception (MP) in primary open-angle glaucoma (POAG). METHOD: Forty-one patients with POAG (67 eyes) and 56 (112 eyes) normal subjects were examined by the motion perception (MP) software in PC compatible computer. RESULTS: The total abnormal rate of MP was 89.5% in POAG, and 81.6% in the early stage of POAG. By using the grade correlation analysis, there is positive correlation of the abnormal degree of MP with C/D, ocular tension, and corrected loss variance (CLV) of visualfield, negative correlation of the abnormal degree of MP with visual acuity and visualfield mean sensitivity (MS), and no correlation of the abnormal degree of MP with age and short-term fluctuation (SF) of visualfield in the POAG patients. CONCLUSION: The examination of MP is a newly reliable and simple test for the diagnosis of the early POAG.

Adolescent↗
PubMed1992

Motion perception and aging.

The authors used a correlated motion paradigm to investigate the effects of aging and gender on motion sensitivity. In 2 experiments with a total of 50 elderly and 50 young subjects, motion thresholds were significantly higher for elderly women. The correlated motion signal, which was embedded in random motion, may have been coherent to subjects in much the same way a form is in Witkin's Embedded Figures Test (EFT). In Experiment 2, EFT scores were obtained. A significant positive relationship between motion thresholds and EFT performance was found within each age group. Although gender-related perceptual style differences may contribute to motion perception effects, the authors argue that a common neural factor contributes to performance on both the EFT and the correlated motion task.

Adult↗
PubMed1990

Intact "biological motion" and "structure from motion" perception in a patient with impaired motion mechanisms: a case study.

A series of psychophysical tests examining early and later aspects of image-motion processing were conducted in a patient with bilateral lesions involving the posterior visual pathways, affecting the lateral parietal-temporal-occipital cortex and the underlying white matter (as shown by magnetic resonance imaging studies and confirmed by neuro-ophthalmological and neuropsychological examinations). Visual acuity, form discrimination, color, and contrast-sensitivity discrimination were normal whereas spatial localization, line bisection, depth, and binocular stereopsis were severely impaired. Performance on early motion tasks was very poor. These include seeing coherent motion in random noise (Newsome & Paré, 1988), speed discrimination, and seeing two-dimensional form from relative speed of motion. However, on higher-order motion tasks the patient was able to identify actions from the evolving pattern of dots placed at the joints of a human actor (Johansson, 1973) as well as discriminating three-dimensional structure of a cylinder from motion in a dynamic random-dot field. The pattern of these results is at odds with the hypothesis that precise metrical comparison of early motion measurements is necessary for higher-order "structure from motion" tasks.

Cerebral Cortex↗
PubMed1993

Spatio-temporal characteristics of human motion perception.

A bi-local detector array model was assumed to describe the functional performance of monocular motion perception. Distributions of model parameters were measured in human vision at several positions in the visual field. The stimulus paradigm was designed to measure directional motion perception thresholds for individual combinations of spatial displacement and temporal delay in random dot apparent motion stimuli. The resulting data support previous results on perceivable spatial displacement limits in human vision but also indicate that both minimum and maximum perceivable spatial displacement thresholds in human observers have a similar dependence on temporal delay. This dependence changes with eccentricity in the visual field in a qualitatively similar manner but by quantitatively different factors. A description of possible biological properties of the bi-local detector population is presented that may explain how detection of spatio-temporal pattern displacements can be performed by a single system. Such a system also predicts that minimum and maximum perceivable spatial displacement thresholds should scale with visual field eccentricity in a manner consistent with our results.

Humans↗
PubMed1994

Motion perception. Moving on the surface.

Recent studies of motion perception show that, in the brain's internal representation of three-dimensional space, distances may be less important than relationships to surfaces.

Brain↗
PubMed1991

Does primate motion perception depend on the magnocellular pathway?

This study examined the importance of the primate magnocellular retinocortical pathway in the perception of moving stimuli. A portion of the magnocellular pathway was permanently and selectively interrupted by ibotenic acid injections in the LGN of macaque monkeys. We then tested contrast sensitivity for detecting moving stimuli, as well as two indices of motion perception, contrast sensitivity for opposite direction discrimination and speed difference thresholds, in the affected portion of the visual field. Magnocellular lesions greatly reduced detection contrast sensitivity at high temporal and low spatial frequencies and had a similar effect on contrast sensitivity for opposite direction discrimination under these same stimulus conditions. Consequently, opposite direction discriminations could be made at contrast threshold, suggesting that magnocellular lesions reduced the visibility of stimuli used to test direction perception, but did not act directly on direction perception. Magnocellular lesions also elevated speed difference thresholds under some stimulus conditions. However, this deficit was reduced or eliminated by raising the contrast of the test stimulus. Together, these findings suggest that magnocellular lesions reduce the visibility of stimuli used to test motion perception but that they do not appear to alter motion perception otherwise.

Animals↗
PubMed1997

Isoluminance and chromatic motion perception throughout the visual field.

Isoluminance and chromatic motion perception for red/green gratings were measured throughout an 80 deg visual field. Generally, the red/green isoluminance values changed with increasing eccentricity, i.e., observers increased the red luminance contrast for a fixed green luminance contrast. Enlarging the target size (to compensate for the cone density changes with eccentricity) and decreasing the spatial frequency (to compensate for receptive field property changes with eccentricity) did not change the isoluminance values within the central 20 deg, but the isoluminance ratios decreased beyond 20 deg. Our manipulations did not entirely compensate for a given eccentricity, which implies the need for a post-receptoral scaling function for the perception of drifting chromatic stimuli. Further, the results for isoluminance show heterogeneity between the visual field meridians where the red to green luminance ratio tends to be greater in the superior visual field. In our present conditions, chromatic motion was always perceived (up to 40 deg of eccentricity), but sensitivity generally decreased with increasing eccentricity. The inferior visual field was found to be the most sensitive to chromatic motion. We propose that the lower visual field and not the superior visual field is specialized for colour motion information.

Color Perception↗
PubMed1994

Neural network approaches to visual motion perception.

This paper concerns certain difficult problems in image processing and perception: neurocomputation of visual motion information. The first part of this paper deals with the spatial physiological integration by the figure-ground discrimination neural network in the visual system of the fly. We have outlined the fundamental organization and algorithms of this neural network, and mainly concentrated on the results of computer simulations of spatial physiological integration. It has been shown that the gain control mechanism, the nonlinearity of synaptic transmission characteristic, the interaction between the two eyes, and the directional selectivity of the pool cells play decisive roles in the spatial physiological integration. In the second part, we have presented a self-organizing neural network for the perception of visual motion by using a retinotopic array of Reichardt's motion detectors and Kohonen's self-organizing maps. It has been demonstrated by computer simulations that the network is able to learn to solve the ambiguities given by local motion detection mechanism. The resultant self-organized configuration in the output layer is resembling direction selective columns which first appear in area MT of the primate visual system. It has been explored that the spatio-temporal coherences, mapping, cooperation, competition, and Hebb rule are the basic neural principles for visual motion perception.

Animals↗
PubMed1993

Motion perception with spatiotemporally matched chromatic and achromatic information reveals a "slow" and a "fast" motion system.

Recent reports dealing with apparent motion challenged the standard view according to which motion processing should be impossible if the visual attributes matched across space and time are processed in independent channels (the similarity principle). The present work examines this possibility insofar as it relates to the spatiotemporal combination of pure chromatic and pure luminance information. The data indicate that the "similarity principle" is indeed infringed at low (< or = 2.5 Hz, i.e. velocities of 2.5 deg/sec for spatial modulations of 1 c/deg, in this study) but not at high (> or = 7.5 Hz) temporal frequencies. The fact that colour and luminance may or may not combine to yield motion perception depending on their temporal modulation reconciliates contradictory results in the literature and supports the idea of two motion systems, a "fast"/specific one, integrating information only from similar subunits, and a "slow"/unspecific one, integrating information across dissimilar subunits (in the present case, across the chromatic and achromatic "domains"). This dichotomy is also supported by the finding that chromatic reverse-phi (i.e. with equiluminant, red and green stimuli) can be observed at medium temporal frequencies but is replaced by direct motion at low temporal frequencies, presumably within the range of the "slow"/unspecific system. Using a modified "minimum motion" technique (referred to as the Reverse-Phi equiluminance method) we present data allowing to assess the relative weights of the two systems as a function of temporal frequency.

Color Perception↗
PubMed1998

Complex motion perception and its deficits.

Within the hierarchy of motion perception, the dorsolateral middle superior temporal area (MSTd) is optimally suited for the analysis of the complex motion patterns that are directly useful for visually guided behaviour (e.g. computation of heading). Recent electrophysiological and psychophysical evidence suggests the existence of 'detectors' in MSTd that are specialised for complex motion patterns and advocates the necessity of combining retinal and extraretinal signals received by MSTd neurones for the accurate perception of heading. In some neurological patients, of which only a small number have been reported to date, lesions involving the human homologue of MST have devastating effects on their ability to navigate in their surroundings. It has been reported that these patients have impaired performance of psychophysical tasks of complex motion discrimination.

Animals↗
PubMed1990

Assimilation and contrast in motion perception: explorations in cooperativity.

Motions within one region of the field influence motion seen elsewhere. To explore this phenomenon we used cinematograms comprised of alternating strips within which dots (i) tended to move in one direction, or (ii) moved in random directions (dynamic noise). When alternating strips were narrow, motion in one direction induced a similar direction of illusory motion in the adjoining dynamic noise (assimilation); when alternating strips were wide, motion tended to induce an illusory opposed motion in the dynamic noise (contrast). Since this illusory motion exhibits hysteresis, it probably results from spatially distributed, cooperative processes. The shift from assimilation to contrast, as the cinematogram's strips increase in size, suggests that facilitatory and inhibitory influences of the network extend over different distances.

Contrast Sensitivity↗