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Development of motion perception in early infancy.

This article summarizes some research on the development of motion perception in early infancy. The sensitivity for slow and rapid motion was studied with 1-month-old and 3-month-old babies. The findings suggest that there are different developmental courses for the detection of slow and rapid motion. The ability to detect very slow motion seems to improve gradually with age whereas the sensitivity for very rapid motion seems to be at a level comparable to adults soon after birth. Three-month-old babies do use kinetic visual information in order to perceive object boundaries and form. After having seen a form visible only when moving they are able to "identify" the same form when seeing it under static conditions. Infants and young children do use kinetic visual information for recognizing figures that are never completely in sight only if they have been familiarized with the fully visible form first. Even 4-year-olds have difficulties in perceiving the full form of a figure that moves behind a slit in an opaque occluding surface if there is no familiarity or "priming" with the global form first. In conclusion, infants are able to detect visual motion very early in life and do extract information which leads to the perception of form. However, this ability may be limited to events with uninterrupted, continuous movement of visible elements.

Age Factors↗

The shape of self-motion perception--I. Equivalence classification for sustained motions.

Two completely different motions of a subject relative to the earth can induce exactly the same stimuli to the vestibular, somatosensory and visual systems. When this happens, the subject may experience disorientation and misperception of self-motion. We have identified large classes of motions that are perceptually equivalent, i.e. indistinguishable by the subject, under three sets of conditions: no vision, with vision and earth-fixed visual surround, and with vision during possible movement of the visual surround. For each of these sets of conditions, we have developed a classification of all sustained motions according to their perceptual equivalences. The result is a complete list of the possible misperceptions of sustained motion due to equivalence of the forces and other direct stimuli to the sensors under the given conditions. This research expands the range of possible experiments by including all components of linear and angular velocity and acceleration. Many of the predictions in this paper can be tested experimentally. In addition, the equivalence classes developed here predict perceptual phenomena in unusual motion environments that are difficult or impossible to investigate in the laboratory.

Humans↗

Constant affine velocity predicts the 1/3 power law of planar motion perception and generation.

Numerous studies have shown that the power of 1/3 is important in relating Euclidean velocity to radius of curvature (R) in the generation and perception of planar movement. Although the relation between velocity and curvature is clear and very intuitive, no valid explanation for the specific 1/3 value has yet been found. We show that if instead of computing the Euclidean velocity we compute the affine one, a velocity which is invariant to affine transformations, then we obtain that the unique function of R which will give (constant) affine invariant velocity is precisely R1/3. This means that the 1/3 power law, experimentally found in the studies of hand-drawing and planar motion perception, implies motion at constant affine velocity. Since drawing/perceiving at constant affine velocity implies that curves of equal affine length will be drawn in equal time, we performed an experiment to further support this result. Results showed agreement between the 1/3 power law and drawing at constant affine velocity. Possible reasons for the appearance of affine transformations in the generation and perception of planar movement are discussed.

Analysis of Variance↗

A reduction in the number of directionally selective neurons extends the spatial limit for global motion perception.

Dynamic random-dot targets were used to study neural mechanisms underlying motion perception. Performance of cats with severely reduced numbers of cortical directionally selective neurons (reduced DS) was compared to that of normal animals. We assessed the spatial properties of the residual motion mechanism by measuring direction discriminations at various dot displacements. At small displacements, reduced DS cats' motion integration thresholds for opposite direction discrimination were nearly normal. At larger displacements, their thresholds surpassed those of normal cats and their upper displacement limit (dmax) was increased by 0.35 deg. The accuracy of direction discrimination was reduced at small displacements, but at larger displacements direction difference thresholds of reduced DS cats approached or surpassed those of normals. These data were compared to the performance of humans who showed an extension of dmax for peripherally viewed targets. The data support the hypothesis that expansion in spatial scale of the motion mechanism may contribute to extension of dmax. Additional support for this hypothesis is provided by a modified direction discriminating line-element model. The model also suggests that changes in sampling of motion mechanisms in the reduced DS system may play a role.

Animals↗

Motion perception in the peripheral visual field.

Literature dealing with the peripheral retina and its 'specialization for motion detection' is reviewed. The data at hand seem to indicate that the central retina is more 'specialized' for motion perception than the peripheral retina. It is clear that motion improves vision for stimuli presented peripherally.

Eye Movements↗

A comparison of the latencies of visually induced postural change and self-motion perception.

This study compared the latencies of visually induced postural change and self-motion perception under identical visual conditions. The results showed that a visual roll stimulus elicits postural tilt in the direction of scene motion and an increase in postural instability several seconds before the subject begins to perceive illusory self-motion (vection) in the opposite direction. Postural and vection latencies correlate highly with one another, but bear little relationship with the magnitude of either sway or vection.

Adolescent↗

Human motion perception and smooth eye movements show similar directional biases for elongated apertures.

Although numerous studies have examined the relationship between smooth-pursuit eye movements and motion perception, it remains unresolved whether a common motion-processing system subserves both perception and pursuit. To address this question, we simultaneously recorded perceptual direction judgments and the concomitant smooth eye-movement response to a plaid stimulus that we have previously shown generates systematic perceptual errors. We measured the perceptual direction biases psychophysically and the smooth eye-movement direction biases using two methods (standard averaging and oculometric analysis). We found that the perceptual and oculomotor biases were nearly identical, suggesting that pursuit and perception share a critical motion processing stage, perhaps in area MT or MST of extrastriate visual cortex.

Humans↗

Cervico-vestibular and visuo-vestibular interaction. Self-motion perception, nystagmus, and gaze shift.

In 8 healthy subjects we studied self-motion perception and nystagmus due to sinusoidal stimulation (amplitude 90 degrees peak to peak, frequency 0.05 Hz) of the horizontal semicircular canals, the cervical proprioceptors, and the retina. We used an electrically driven rotatory chair and optokinetic drum combination. For cervical stimulation the subject's head was placed in a clamp, attached to the drum. Eye movements were recorded by means of electrooculography, d.c. amplification. Subjects signalled the estimated head position by means of a 'joystick'. In the present series of experiments the vestibular and cervical informations were played off against each other in combined stimulation conditions with an interstimulus phase lag of 0 to 315 degrees, in steps of 45 degrees. Similarly, the vestibular and visual informations were played off against each other. Concerning estimated head position, our main finding is that both the visually and the cervically induced illusion of head rotation overrule the vestibular sensation of head motion. The ocular response to combined vestibular plus cervical stimulation shows that both nystagmus slow phases and saccades of the cervical and the vestibular responses add up by vectorial summation.

Adult↗

Interaction of vestibular and proprioceptive inputs for human self-motion perception.

Human perception of horizontal self(body)-motion in space was studied during various combinations of vestibular and leg-proprioceptive stimuli in the dark. During sinusoidal rotations of the trunk relative to the stationary feet (functionally synergistic combination) the perception was almost veridical over the frequency range tested (0.025-0.4 Hz). This finding suggested a dominance of the proprioceptive over the vestibular input, since the quantitative aspects of the perception (gain, phase, and detection threshold): (a) closely resembled those of the proprioceptive foot-to-trunk perception, and (b) clearly differed from those of the vestibular self-motion perception. However, when using other combinations, the self-motion perception changed in a monotonous way as a function of the two inputs, indicating that the two inputs do interact in a linear way. In a model of these findings the interaction occurs in two stages: (1) summation of a vestibular trunk-in-space signal and a (dynamically matched) proprioceptive foot-to-trunk signal yields an internal representation of foot support motion in space; (2) superposition of the latter by an almost ideal proprioceptive trunk-to-foot signal results in a representation of trunk-in-space motion (essentially proprioception-dependent and ideal when the feet are stationary).

Foot↗

A study of motion perception in primary open angle glaucoma.

PURPOSE: To study the features of the motion perception (MP) and explore the worth of the clinical application of MP test in primary open angle glaucoma (POAG). METHODS: MPs were recorded from 41 patients (67 eyes) with POAG ang 56 normal subjects (112 eyes) by the MP software in PC compatible computer. Meanwhile, the MP ways and MP sites were analyzed and MP abnormal rate was compared to the clinical parameters and the visual function indices related to glaucoma. RESULTS: The results showed that the total abnormal rate of MP was 89.5% in POAG, and the abnormal rate was 81.6% in early stage of POAG, and MP abnormal degree had positive correlation with C/D, ocular tension and corrected loss variance (CLV), and negative correlation with visual acuity and mean sensitivity (MS), and no correlation with age and short-term fluctuation (SF) in the patients with POAG. CONCLUSION: These results suggest that the MP test provides a newly effective examination method in diagnosing the early POAG.

Adolescent↗

Binocular rivalry and motion perception.

In a series of experiments psychophysical techniques were used to study the relation between binocular rivalry and motion perception. An initial series of experiments confirmed that motion enhances the predominance of an eye during rivalry, although the direction of motion does not matter. The presence of an annulus of motion immediately surrounding one eye's rival target greatly enhances dominance of that target, but the influence of the annulus progressively decreases as the separation between disk and annulus increased. Opponent directions of motion in disk and annulus yield greater dominance than when dots in the disk and annulus moved in identical directions. In a second experiment that two eyes were adapted to orthogonal directions of motion, generating strong, distinctively different monocular motion aftereffects (MAEs). Even though the two eyes view physically identical random-motion displays following differential adaptation, binocular rivalry of the discrepant MAEs can occur. Finally, using a stimulus replacement technique to measure detectability of translational and rotational motion, it was found that both types of motion were readily detected during periods of dominance but went undetected during periods of suppression. Taken together, these results bear on the process responsible for rivalry and its neural locus relative to the analysis of different types of motion.

Adaptation, Ocular↗

Computational aspects of motion perception in natural and artificial vision systems.

In this paper a computational scheme for motion perception in artificial and natural vision systems is described. The scheme is motivated by a mathematical analysis in which first-order spatial properties of optical flow, such as singular points and elementary components of optical flow, are shown to be salient features for the computation and analysis of visual motion. The fact that different methods for the computation of optical flow produce similar results is explained in terms of the simple spatial structure of the image motion of rigid bodies. Singular points and elementary flow components are used to compute motion parameters, such as time-to-collision and angular velocity, and also to segment the visual field into areas which correspond to different motions. Then a number of biological implications are discussed. Electrophysiological findings suggest that the brain perceives visual motion by detecting and analysing optical flow components. However, the cortical neurons, which seem to detect elementary flow components, are not able to extract these components from more complex flows. A simple model for the organization of the receptive field of these cells, which is consistent with anatomical and electrophysiological data, is described at the end of the paper.

Artificial Intelligence↗

Spatial summation and its interaction with the temporal integration mechanism in human motion perception.

The combination of visual motion information over visual space (spatial summation) and stimulus duration (temporal integration) was investigated using a random-pixel array (spatiotemporally broad-band) apparent motion stimulus designed to isolate specific populations of visual motion detectors. The results indicate that, in agreement with results from spatiotemporally narrow-band stimuli, spatial summation follows the form of linear probabilistic summation rather than non-linear probabilistic summation. Linear probabilistic summation holds for a wide range of stimulus parameters and when changing either motion stimulus height or width. Linear probabilistic summation breaks down when the motion display region approaches a height and/or width that is related to the spatial displacement size, not the speed, of the random-pixel array. This height and width (termed the critical height and width, or critical dimension), increases with spatial displacement size and can be interpreted as a measure of the basic dimensions of the selected motion detector population's receptive field. The critical height is smaller than the critical width, a result that is consistent with a motion detector receptive field that is elongated in the direction of motion. Perhaps most importantly, the mechanisms of temporal integration and spatial summation can work independently under a wide range of conditions. Finally, the results provide evidence for a short-term inhibitory phenomenon from the edges of the useful display area that affects the visibility of the motion.

Contrast Sensitivity↗

Motion perception: a modern view of Wertheimer's 1912 monograph.

Max Wertheimer's 1912 monograph on apparent motion is a seminal contribution to the study of visual motion, but its actual contents are not widely known. This article attempts to clarify what the monograph did and did not contribute, emphasizing links between Wertheimer's principal findings and the results of subsequent investigations of motion perception, including currently active lines of research. The topics discussed include Wertheimer's experimental tests of explanations for apparent motion; his work with motion phenomena that lie between succession and optimum motion; his studies of the influence of attention on motion; explorations of various forms of hysteresis and motion transparency; and Wertheimer's work with a motion-blind patient.

History, 20th Century↗

New aspects of motion perception: selective neural encoding of apparent human movements.

Perception of apparent motion operates somewhat differently for objects and human figures. Depending on the interstimulus interval, the latter d may give rise to either perception of a direct path (i.e. biologically impossible) or indirect path (i.e. biologically possible). Here, PET was used to investigate whether a change in brain activity accompanies this perceptual shift. We found neural encoding of apparent motion to be a function of the intrinsic properties of the stimulus presented (object vs human) as well as the kind of human movement path perceived (biomechanically possible vs impossible). Motor and parietal cortex were only involved for possible motion which suggests that these regions are selectively activated to process actions which conform to the capabilities of the observer.

Adult↗

Motion perception in schizophrenia.

BACKGROUND: Eye-tracking dysfunction has been found in many patients with schizophrenia and in about 40% of their first-degree biological relatives. We hypothesized that a deficit in motion processing is associated with eye-tracking dysfunction because both motion signals and the brain regions responsible for processing motion signals are implicated in the generation of smooth pursuit. We examined several aspects of visual perception, including motion perception, in patients with schizophrenia. METHODS: To evaluate motion perception, contrast sensitivity for velocity discrimination was measured in patients with schizophrenia (n=15) and normal control subjects (n=18). Contrast sensitivities for orientation discrimination and contrast detection were measured as control tasks. RESULTS: Patients with schizophrenia showed significantly lower contrast sensitivity (ie, higher thresholds) than normal controls for the discrimination of small velocity differences (eg, 11 vs 9 degrees/s). This reduction in contrast sensitivity was severe (up to 10-fold) in about 40% of the patients. No group differences were found on the other tasks. CONCLUSION: The discrimination of small velocity differences is impaired in a subgroup of patients with schizophrenia.

Brain↗

'Generic-view principle' for three-dimensional-motion perception: optics and inverse optics of a moving straight bar.

The generic-view principle (GVP) states that given a 2-D image the visual system interprets it as a generic view of a 3-D scene when possible. The GVP was applied to 3-D-motion perception to show how the visual system decomposes retinal image motion into three components of 3-D motion: stretch/shrinkage, rotation, and translation. First, the optical process of retinal image motion was analyzed, and predictions were made based on the GVP in the inverse-optical process. Then experiments were conducted in which the subject judged perception of stretch/shrinkage, rotation in depth, and translation in depth for a moving bar stimulus. Retinal-image parameters-2-D stretch/shrinkage, 2-D rotation, and 2-D translation-were manipulated categorically and exhaustively. The results were highly consistent with the predictions. The GVP seems to offer a broad and general framework for understanding the ambiguity-solving process in motion perception. Its relationship to other constraints such as that of rigidity is discussed.

Bayes Theorem↗

Effects of prolonged weightlessness on self-motion perception and eye movements evoked by roll and pitch.

Seven astronauts reported translational self-motion during roll stimulation 1-3 h after landing following 5-7 d of orbital flight. Two reported strong translational self-motion perception when they performed pitch head motions during entry and while the orbiter was stationary on the runway. One of two astronauts from whom adequate data were collected exhibited a 132 degrees shift in the phase angle between roll stimulation and horizontal eye position 2 h after landing. Neither of two from whom adequate data were collected exhibited increased horizontal eye movement amplitude or disturbance of voluntary pitch or roll body motion immediately postflight. These results are generally consistent with an otolith tilt-translation reinterpretation model and are being applied to the development of apparatus and procedures intended to preadapt astronauts to the sensory rearrangement of weightlessness.

Electrooculography↗