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Two-dimensional motion perception without feature tracking.

Feature-tracking explanations of 2D motion perception are fundamentally distinct from motion-energy, correlation, and gradient explanations, all of which can be implemented by applying spatiotemporal filters to raw image data. Filter-based explanations usually suffer from the aperture problem, but 2D motion predictions for moving plaids have been derived from the intersection of constraints (IOC) imposed by the outputs of such filters, and from the vector sum of signals generated by such filters. In most previous experiments, feature-tracking and IOC predictions are indistinguishable. By constructing plaids in apparent motion from missing-fundamental gratings, we set feature-tracking predictions in opposition to both IOC and vector-sum predictions. The perceived directions that result are inconsistent with feature tracking. Furthermore, we show that increasing size and spatial frequency in Type 2 missing-fundamental plaids drives perceived direction from vector-sum toward IOC directions. This reproduces results that have been used to support feature-tracking, but under experimental conditions that rule it out. We discuss our data in the context of a Bayesian model with a gradient-based likelihood and a prior favoring slow speeds. We conclude that filter-based explanations alone can explain both veridical and non-veridical 2D motion perception in such stimuli.

Adult↗

Changes in visual motion perception before saccadic eye movements.

Execution of a saccadic eye movement influences subsequent motion perception [Park, J., Lee, J., & Lee, C. (2001). Non-veridical visual motion perception immediately after saccades. Vision Research, 41, 3751-3761]. In the current study, we determined the pattern of perceptual changes for visual motion presented before saccades. The accuracy of judging the direction of a moving target was variable depending on the direction of target motion. Based on the pattern of judgment errors, the direction associated with no error, or DNE, could be defined. When a moving target was seen by stationary eyes, the DNE was roughly vertical, and the perceptual judgment for adjacent directions was biased away from the vertical direction. When the same visual motion was seen before horizontal saccades, the DNE shifted in the direction of the impending saccade, and the perceptual judgment of adjacent directions was shifted away from the new DNE, thus, shifting the perceived direction of the vertical in the direction opposite to the saccade. These changes improved the accuracy of direction judgment for visual motion in the visual field ipsiversive to impending saccades. In addition to shift of the DNE, perceptual judgment for oblique directions became near veridical before saccades, which we call the anti-oblique effect. These results suggest that motion perception is dynamically and anisotropically modulated at the time of saccades, and the DNE shift may be a part of processes dynamically reallocating computational resources, improving perceptual performance in advance for sensory events to be acquired by impending saccades.

Adult↗

Motion perception during dichoptic viewing of moving random-dot stereograms.

The relation between binocular and monocular motion perception was investigated. A random-dot stereogram (30 X 30 deg arc), containing a central figure seen in front of the background in stereoscopic vision, was viewed dichoptically by human subjects without a fixed visual frame of reference. The images seen by the right and left eye were moved laterally according to a triangular wave form, in counterphase, but with variable amplitude ratios. Under this condition only purely lateral movement and no motion in depth of the stereogram as a whole was perceived, while stereoscopic vision of the figure-background relation was maintained. The magnitude of the binocularly perceived lateral motion, signalled by manual tracking of the perceived displacement, equalled the algebraic mean of the monocular motion percepts. As a special case, when the two images forming the stereogram were moved with equal velocities but in opposite directions they were perceived as a completely stationary, fused image in stereoscopic depth. Only the addition of a stationary reference (a bar or grating seen by both eyes) resulted in the perception of motion in depth. We conclude that a visual frame of reference is essential for perception of motion in depth but not for perception of lateral movements. Moreover, it seems likely that not absolute binocular disparity (retinal locus differences) but relative binocular disparity (differences in angular distance between two or more corresponding features in the two retinal images) is a cue for perception of depth.

Convergence, Ocular↗

Gibson's inspired but latent prelude to visual motion perception.

Gibson's 1954 article is paradoxical: This forward-looking review of visual motion perception anticipates developments in the field, yet those developments were achieved without closely following Gibson's footsteps. This commentary offers several possible reasons for the dormancy of Gibson's ideas about motion perception and evaluates contemporary work on motion perception in the context of Gibson's perspective.

History, 20th Century↗

Blindsight modulation of motion perception.

Monkey data suggest that of all perceptual abilities, motion perception is the most likely to survive striate damage. The results of studies on motion blindsight in humans, though, are mixed. We used an indirect strategy to examine how responses to visible stimuli were modulated by blind-field stimuli. In a 26-year-old man with focal striate lesions, discrimination of visible optic flow was enhanced about 7% by blind-field flow, even though discrimination of optic flow in the blind field alone (the direct strategy) was at chance. Pursuit of an imagined target using peripheral cues showed reduced variance but not increased gain with blind-field cues. Preceding blind-field prompts shortened reaction times to visible targets by about 10 msec, but there was no attentional crowding of visible stimuli by blind-field distractors. A similar efficacy of indirect blind-field optic flow modulation was found in a second patient with residual vision after focal striate damage, but not in a third with more extensive medial occipito-temporal damage. We conclude that indirect modulatory strategies are more effective than direct forced-choice methods at revealing residual motion perception after focal striate lesions.

Adult↗

Visual contributions to human self-motion perception during horizontal body rotation.

It is still an enigma how human subjects combine visual and vestibular inputs for their self-motion perception. Visual cues have the benefit of high spatial resolution but entail the danger of self motion illusions. We performed psychophysical experiments (verbal estimates as well as pointer indications of perceived self-motion in space) in normal subjects (Ns) and patients with loss of vestibular function (Ps). Subjects were presented with horizontal sinusoidal rotations of an optokinetic pattern (OKP) alone (visual stimulus; 0.025-3.2 Hz; displacement amplitude, 8 degrees) or in combinations with rotations of a Bárány chair (vestibular stimulus; 0.025-0.4 Hz; +/- 8 degrees). We found that specific instructions to the subjects created different perceptual states in which their self-motion perception essentially reflected three processing steps during pure visual stimulation: i) When Ns were primed by a procedure based on induced motion and then they estimated perceived self-rotation upon pure optokinetic stimulation (circular vection, CV), the CV has a gain close to unity up to frequencies of almost 0.8 Hz, followed by a sharp decrease at higher frequencies (i.e., characteristics resembling those of the optokinetic reflex, OKR, and of smooth pursuit, SP). ii) When Ns were instructed to "stare through" the optokinetic pattern, CV was absent at high frequency, but increasingly developed as frequency was decreased below 0.1 Hz. iii) When Ns "looked at" the optokinetic pattern (accurately tracked it with their eyes) CV was usually absent, even at low frequency. CV in Ps showed similar dynamics as in Ns in condition i), independently of the instruction. During vestibular stimulation, self-motion perception in Ns fell from a maximum at 0.4 Hz to zero at 0.025 Hz. When vestibular stimulation was combined with visual stimulation while Ns "stared through" OKP, perception at low frequencies became modulated in magnitude. When Ns "looked" at OKP, this modulation was reduced, apart from the synergistic stimulus combination (OKP stationary) where magnitude was similar as during "staring". The obtained gain and phase curves of the perception were incompatible with linear systems prediction. We therefore describe the present findings by a non-linear dynamic model in which the visual input is processed in three steps: i) It shows dynamics similar to those of OKR and SP; ii) it is shaped to complement the vestibular dynamics and is fused with a vestibular signal by linear summation; and iii) it can be suppressed by a visual-vestibular conflict mechanism when the visual scene is moving in space. Finally, an important element of the model is a velocity threshold of about 1.2 degrees/s which is instrumental in maintaining perceptual stability and in explaining the observed dynamics of perception. We conclude from the experimental and theoretical evidence that self-motion perception normally is related to the visual scene as a reference, while the vestibular input is used to check the kinematic state of the scene; if the scene appears to move, the visual signal becomes suppressed and perception is based on the vestibular cue.

Adult↗

Direct current stimulation over V5 enhances visuomotor coordination by improving motion perception in humans.

The primary aim of this study was to determine the extent to which human MT+/V5, an extrastriate visual area known to mediate motion processing, is involved in visuomotor coordination. To pursue this we increased or decreased the excitability of MT+/V5, primary motor, and primary visual cortex by the application of 7 min of anodal and cathodal transcranial direct current stimulation (tDCS) in healthy human subjects while they were performing a visuomotor tracking task involving hand movements. The percentage of correct tracking movements increased specifically during and immediately after cathodal stimulation, which decreases cortical excitability, only when V5 was stimulated. None of the other stimulation conditions affected visuomotor performance. We propose that the improvement in performance caused by cathodal tDCS of V5 is due to a focusing effect on to the complex motion perception conditions involved in this task. This hypothesis was proven by additional experiments: Testing simple and complex motion perception in dot kinetograms, we found that a diminution in excitability induced by cathodal stimulation improved the subject's perception of the direction of the coherent motion only if this was presented among random dots (complex motion perception), and worsened it if only one motion direction was presented (simple movement perception). Our data suggest that area V5 is critically involved in complex motion perception and identification processes important for visuomotor coordination. The results also raise the possibility of the usefulness of tDCS in rehabilitation strategies for neurological patients with visuomotor disorders.

Adult↗

Global motion perception: no interaction between the first- and second-order motion pathways.

The experiments reported here address the issue of whether the pathways which extract motion from first-order and second-order spatial patterns remain separate or whether they combine at some higher level in the motion system to form a single pathway. The question is addressed by investigating the interaction of first-order and second-order stimuli in the processing of a global-motion stimulus [a variant of the task introduced by Newsome & Pare (Journal of Neuroscience, 8, 2201-2211, (1988)]. Two experimental procedures were used. The first consisted of determining the effect of the addition of dots of one type (e.g. first order) undergoing purely random motion on the ability to extract the global-motion signal carried by dots of the other type (e.g. second order). The second experimental procedure consisted of determining the effect of maintaining a coherent-motion signal in one type of dot, moving in the opposite direction to the global-motion direction, on the ability to extract the global-motion signal carried by dots of the other type. The dots were matched for their effectiveness in producing a global motion percept and the results for both procedures were the same. First-order dots impaired the ability to extract second-order global-motion, and second-order dots had no effect on first-order global-motion extraction. It is argued that the sensitivity of the second-order global-motion system to the first-order dots is due to the ability of the second-order local-motion detectors to detect these dots. The present results are thus interpreted as indicating that the first-order and second-order motion pathways remain separate up to and including the level in the motion system at which global-motion signals are extracted.

Humans↗

Temporal structure of the apparent motion perception: a magnetoencephalographic study.

Humans perceive motion when numerous small dots pattern is followed by one of the same pattern but with all the dots shifted a little in one direction. When the amount of shift exceeds a level humans no more perceive motion even though physical visual information does not change. Using this stimulus, we addressed to elucidate the temporal structure of the neural activity related to this apparent motion perception. The magnetic responses to the random-dot patterns with various amounts of shift were measured while the subjects were performing a direction discrimination task. A significant magnetic response amplitude change occurred with three distinct peaks when the response inducing apparent motion was compared with those inducing no motion without change in the response latencies. The major difference occurred at about 110, 140, 210 ms after the stimulus onset. The response origin was always within the occipitotemporal area. The results indicate that the neural activity for the perception of apparent motion can be measured by MEG that occur at least 110 ms after the stimulus onset possibly in the human MT+. Three distinct peaks in the response difference may represent the sequential multiple neural process proposed theoretically though further study is necessary to prove.

Adult↗

The relationship between smooth pursuit performance, motion perception and sustained visual attention in patients with schizophrenia and normal controls.

BACKGROUND: In this study, we tested the hypothesis that low smooth pursuit gain in schizophrenia is related to an abnormality in motion perception. METHODS: The subjects were 19 schizophrenics treated with clozapine and 19 controls. In addition to smooth pursuit and motion perception paradigms, sustained attention was also assessed using a continuous performance task (CPT). RESULTS: In the patient group, there was a statistically significant negative correlation between smooth pursuit gain and motion perception threshold (r = -0.60, P < 0.01). This relationship was not secondary to attention deficits as assessed by the CPT. CONCLUSIONS: Our results are consistent with the notion that the smooth pursuit gain deficit is related to a deficit in motion perception rather than in attention. Brain area V5 (also referred to as "MT' in macaque), located in the parieto-occipital region, is known to be critically important both for motion perception and gain. Thus, our results point to an abnormality in this area in schizophrenia.

Adult↗

Human self-motion perception during translatory vestibular and proprioceptive stimulation.

Self-motion perception in space was studied in normal human subjects during passive vestibular stimulation (lateral translation of whole body in space), proprioceptive stimulation (of feet relative to trunk) and combinations thereof with the eyes closed. Stimulation was sinusoidal, +/- 10 cm, over a frequency range of 0.025-0.4 Hz. Vestibular self-motion perception became increasingly underestimated at low frequency, due to a rather high detection threshold. Proprioceptive stimulation at low frequency elicited a small self-motion illusion. During body translation relative to the stationary feet (vestibular-proprioceptive combination) the magnitude of perceived self-motion was constant across frequency and its threshold was low, as if determined by proprioception alone. Nevertheless, the results can be interpreted in terms of a vestibular-proprioceptive interaction, in analogy to previous findings for rotational stimuli.

Evoked Potentials, Somatosensory↗

Self-motion perception: assessment by real-time computer-generated animations.

We report a new procedure for assessing complex self-motion perception. In three experiments, subjects manipulated a 6 degree-of-freedom magnetic-field tracker which controlled the motion of a virtual avatar so that its motion corresponded to the subjects' perceived self-motion. The real-time animation created by this procedure was stored using a virtual video recorder for subsequent analysis. Combined real and illusory self-motion and vestibulo-ocular reflex eye movements were evoked by cross-coupled angular accelerations produced by roll and pitch head movements during passive yaw rotation in a chair. Contrary to previous reports, illusory self-motion did not correspond to expectations based on semicircular canal stimulation. Illusory pitch head-motion directions were as predicted for only 37% of trials; whereas, slow-phase eye movements were in the predicted direction for 98% of the trials. The real-time computer-generated animations procedure permits use of naive, untrained subjects who lack a vocabulary for reporting motion perception and is applicable to basic self-motion perception studies, evaluation of motion simulators, assessment of balance disorders and so on.

Adult↗

Interaction between primary and secondary mechanisms in human motion perception.

Two layers of information processing can be distinguished as being involved in human motion perception. The primary motion detection stage processes displacements of the luminance distribution across space, such as experienced in natural scenes during the pursuit of moving targets. Primary motion detection is often investigated with artificial motion stimuli realized as random-dot kinematograms (RDKs). Such stimuli belong to the class of "Fourier motion", and their perception can be easily explained by means of elementary motion detectors (EMDs) of the correlation type. Other tasks require the comparison of motion signals from neighbouring areas in the visual field. The perception of the displacement of the motion distribution, for instance, has been accounted for by a secondary motion processing stage. In order to understand the principles of interaction between the motion in neighbouring areas of the visual field, we investigated the sensitivity of the human visual system for moving objects which are defined by moving dots in variable directions. These experiments lead to "secondary tuning curves" of direction discrimination for secondary motion as function of primary motion direction. A base level of sensitivity for all dot motion directions without a velocity component in the same direction of the object movement is enhanced when the object and the dots have a common velocity component. Thus primary motion in any direction can be exploited by the secondary stage, and primary and secondary system both feed into the object motion percept. Furthermore it is suggested from the shape of the secondary tuning curve that the outputs from the two layers of motion processing do not superimpose linearly, but are combined by some sort of veto-like mechanism which increases the directional sensitivity when the two processing layers experience movement along the same direction.

Adult↗

Deficits and recovery of first- and second-order motion perception in patients with unilateral cortical lesions.

Unilateral lesions in the posterior parietal cortex can degrade motion perception in the contralesional visual hemifield. Our aim was to investigate whether deficits caused by cortical lesions may be different for first- and second-order motion perception, and to study the time scale of any potential recovery. In nine patients with circumscribed lesions mainly in the parietal and fronto-parietal cortex, thresholds for direction discrimination were measured for stimuli presented peripherally in their ipsi- and contralesional hemifield. Subjects had to identify the direction of a vertically moving object embedded in a background of dynamic random dot noise. The object consisted of various proportions of signal and noise dots. Signal dots were either (a) coherently moving in the same direction as the object (first-order), (b) stationary (second-order: drift-balanced), or (c) coherently moving in the opposite direction (second-order: theta). Noise dots were flickering. Two patients showed significant threshold elevations for all three types of motion stimuli presented in their contralesional hemifield, while thresholds for ipsilesional targets were unaffected. Neither showed any selective deficit of first- versus second-order motion perception, but second-order motion was more impaired. Their lesions probably included the motion area V5-MT, which was spared in the other seven patients. One of the patients, who was retested several times during a 27-month postlesional period, showed complete recovery for first- and second-order motion direction discrimination, as well as for the detection of speed differences.

Adult↗

Some additional predictions and further tests of the Marr-Ullman model of motion perception.

The Marr-Ullman model for motion detection in the human visual system functions by means of the dual input of polarity-specific edge detectors and luminance change detectors. Moulden and Begg (1986) found a polarity-specific motion aftereffect which they claimed provided support for this dual input model. The logic of their experiment is examined, and it is shown that several additional predictions arise from the Marr-Ullman model, which were not supported by Moulden and Begg's study. A more powerful experiment was carried out and these additional predictions were disconfirmed, although the polarity-specific effect did emerge. A consideration of alternative explanations of this effect led to a second experiment in which an attempt was made to discover the actual determinants of the effect. This revealed that polarity-specific units are unlikely to play any part in the phenomenon. It was concluded, in the light of this and other evidence, that one of a class of alternative models is more likely to be the actual mechanism for motion perception. However, careful consideration of the Marr-Ullman model indicated that it may be untestable in principle if various differentially weighted levels of neural integration are envisaged.

Attention↗

Motion perception deficits from midline cerebellar lesions in human.

Although visual motion processing is commonly thought to be mediated solely by visual cortical areas, this human lesion study suggests that the cerebellum also has a role. We found motion direction discrimination deficits in a group of patients with acute midline cerebellar lesions. Unlike normals and patients with hemispheric cerebellar lesions, these patients with midline lesions were unable to discern a global motion vector in a local stochastic motion display. This resembles the perceptual defect reported following cortical area MT lesions in primates. This motion perception deficit may result from damage to a cerebellar mechanism involved in perceptual stabilization. Disruption of this comparator mechanism is sufficient to produce a severe motion perception deficit even though cortical visual processing mechanisms are still intact.

Adult↗

Attentional modulation of self-motion perception.

Attentional effects on self-motion perception (vection) were examined by using a large display in which vertical stripes containing upward or downward moving dots were interleaved to balance the total motion energy for the two directions. The dots moving in the same direction had the same colour, and subjects were asked to attend to one of the two colours. Vection was perceived in the direction opposite to that of non-attended motion. This indicates that non-attended visual motion dominates vection. The attentional effect was then compared with effects of relative depth. Clear attentional effects were again found when there was no relative depth between dots moving in opposite directions, but the effect of depth was much stronger for stimuli with a relative depth. Vection was mainly determined by motion in the far depth plane, although some attentional effects were evident even in this case. These results indicate that attentional modulation for vection exists, but that it is overridden when there is a relative depth between the two motion components.

Adult↗

Motion-perception deficits and reading impairment: it's the noise, not the motion.

We tested the hypothesis that deficits on sensory-processing tasks frequently associated with poor reading and dyslexia are the result of impairments in external-noise exclusion, rather than motion perception or magnocellular processing. We compared the motion-direction discrimination thresholds of adults and children with good or poor reading performance, using coherent-motion displays embedded in external noise. Both adults and children who were poor readers had higher thresholds than their respective peers in the presence of high external noise, but not in the presence of low external noise or when the signal was clearly demarcated. Adults' performance in high external noise correlated with their general reading ability, whereas children's performance correlated with their language and verbal abilities. The results support the hypothesis that noise-exclusion deficits impair reading and language development and suggest that the impact of such deficits on the development of reading skills changes with age.

Adolescent↗