Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Motion Perception”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 739 records · Page 41Linked to original sources
PubMed2006

When motion appears stopped: stereo motion standstill.

Motion standstill is different from the usual perceptual experiences associated with objects in motion. In motion standstill, a pattern that is moving quite rapidly is perceived as being motionless, and yet its details are not blurred but clearly visible. We revisited motion standstill in dynamic random-dot stereograms similar to those first used by Julesz and Payne [Julesz B, Payne R (1968) Vision Res 8:433-444]. Three improvements were made to their paradigm to avoid possible confounds: The temporal frequency of the motion stimuli was manipulated independently from that of individual stereo gratings so that the failure of motion perception is not due to inability to compute stereo. The motion of the stereo gratings was continuous across the visual field so that the perceived pattern in motion standstill was not a simple average of a back-and-forth display wobble over time. Observers discriminated three spatial frequencies to demonstrate pattern recognition. Three objective psychophysical methods, instead of merely self-report, were used to objectively demonstrate motion standstill. Our results confirm that motion standstill occurs in dynamic random-dot stereogram motion displays at 4-6 Hz. Motion standstill occurs when the stimulus spatiotemporal frequency combination exceeds that of the salience-based third-order motion system in a spatiotemporal frequency range in which the shape and depth systems still function. The ability of shape systems to extract a representative image from a series of moving samples is a significant component of a biological system's ability to derive a stable perceptual world from a constantly changing visual environment.

Adult↗
PubMed1999

Functional magnetic resonance imaging in the visual system.

Functional magnetic resonance imaging (fMRI) is a relatively new technique for measuring brain function during resting and activated conditions with good spatial and temporal resolution. Because of a robust and reproducible activation response to visual stimuli in the occipital cortex, many studies have been directed at visual function. The methodology has been refined progressively to allow more accurate detection of the small activation signal, and using computational mapping foci of cerebral activity have been displayed in a two-dimensional format. Several factors modifying the activation signal have been identified. fMRI has been used to define the retinotopic representation of areal boundaries and the localization of higher visual functions in the occipital cortex. Motion perception in area middle temporal (MT) is well-recognized, but eye movement studies are limited. The activated signal may have significant implications for our understanding of brain metabolism, but cerebral blood flow and oxygenation sensitive recordings after prolonged visual stimulation have given conflicting results. Clinically, fMRI can follow changes in cerebral activity during a progressive neurologic illness and measure responses to treatment. Neurosurgical planning in disorders such as epilepsy may be facilitated.

Color Perception↗
PubMed1992

Roll, pitch, longitudinal and yaw vection visually induced by optical flow in flight simulation conditions.

The present experiment was undertaken to study the effect of the addition of stimulation in the peripheral visual field on perceived self-motion (vection). The parameters were axes of motion, "Central + Peripheral" versus "Central vision, frequencies of sinusoidal motion (0.2 Hz to 1.0 Hz), and amplitudes. Vection generally increased with increased amplitudes and frequencies. In the "Central + Peripheral" condition, there was an interaction between frequencies and amplitudes. When stimuli were presented in "Central" vision only, vection was generally higher. It has been concluded that, for vection, the addition of visual stimulation in the periphery is more important at low sinusoidal frequencies and high amplitudes; at higher frequencies, this produces a decrease in vection probably attributable to an increase in object motion perception.

Adult↗
PubMed2001

Neural dynamics of motion integration and segmentation within and across apertures.

A neural model is developed of how motion integration and segmentation processes, both within and across apertures, compute global motion percepts. Figure-ground properties, such as occlusion, influence which motion signals determine the percept. For visible apertures, a line's terminators do not specify true line motion. For invisible apertures, a line's intrinsic terminators create veridical feature-tracking signals. Sparse feature-tracking signals can be amplified before they propagate across position and are integrated with ambiguous motion signals within line interiors. This integration process determines the global percept. It is the result of several processing stages: directional transient cells respond to image transients and input to a directional short-range filter that selectively boosts feature-tracking signals with the help of competitive signals. Then, a long-range filter inputs to directional cells that pool signals over multiple orientations, opposite contrast polarities, and depths. This all happens no later than cortical area MT. The directional cells activate a directional grouping network, proposed to occur within cortical area MST, within which directions compete to determine a local winner. Enhanced feature-tracking signals typically win over ambiguous motion signals. Model MST cells that encode the winning direction feed back to model MT cells, where they boost directionally consistent cell activities and suppress inconsistent activities over the spatial region to which they project. This feedback accomplishes directional and depthful motion capture within that region. Model simulations include the barberpole illusion, motion capture, the spotted barberpole, the triple barberpole, the occluded translating square illusion, motion transparency and the chopsticks illusion. Qualitative explanations of illusory contours from translating terminators and plaid adaptation are also given.

Computer Simulation↗
PubMed1988

Ground-based training for the stimulus rearrangement encountered during spaceflight.

Approximately 65-70% of the crew members now experience motion sickness of some degree during the first 72 h of orbital flight on the Space Shuttle. Lack of congruence among signals from spatial orientation systems leads to sensory conflict, which appears to be the basic cause of space motion sickness. A project to develop training devices and procedures to preadapt astronauts to the stimulus rearrangements of microgravity is currently being pursued. The preflight adaptation trainers (PATs) are intended to: demonstrate sensory phenomena likely to be experienced in flight, allow astronauts to train preflight in an altered sensory environment, alter sensory-motor reflexes, and alleviate or shorten the duration of space motion sickness. Four part-task PATs are anticipated. The trainers are designed to evoke two adaptation processes, sensory compensation and sensory reinterpretation, which are necessary to maintain spatial orientation in a weightless environment. Recent investigations using one of the trainers indicate that self-motion perception of linear translation is enhanced when body tilt is combined with visual surround translation, and that a 270 degrees phase angle relationship between tilt and surround motion produces maximum translation perception.

Adaptation, Physiological↗
PubMed1992

Perception of optical flow in cortical blindness: a case report.

Motion perception was studied in a subject with bilateral lesion of the visual cortex, involving severe damage to cortical areas V1 and V4, but with no apparent damage to visual associative areas situated in occipito-parietal and lateral occipito-temporal (presumably V5) zones. He was able to perceive optical flow motions simulating motion in depth in "blind" parts of his visual field, provided that the stimulus-onset was temporally dissociated from its motion. Moreover, he was able to discriminate between different velocities and directions of motion. The results suggest that perimetrically "blind" parts of the visual field in this patient have true capacities to process visual motion. They are discussed in reference to the subject's ability to move freely in his environment and in reference to the role of extrastriate visual pathways in visual motion processing.

Acceleration↗
PubMed2006

The effects of optical blur on motion and texture perception.

PURPOSE: The purpose of this study is to determine how decreased visual acuity affects performance on tasks of motion and texture perception. METHODS: Positive diopter lenses were used to match three subjects at five levels of decimal visual acuity (DVA) ranging from an uncorrected DVA of 1.6 to the lowest DVA of 0.2. Performance thresholds were determined at each acuity level for five different psychophysical tasks. The tasks assessed the perception of motion-defined form, global motion, maximum motion displacement (Dmax), texture-defined form, and global texture. RESULTS: Reducing visual acuity decreased performance on the tasks of motion-defined form identification, texture-defined form identification, and global texture integration. Performance on the Dmax task improved with a reduction in visual acuity. Performance on the global motion task was unaffected by changes in visual acuity. CONCLUSIONS: Visual acuity should be considered when interpreting the results of developmental or clinical studies of motion and texture perception. The only exception to this is global motion perception, at least when DVA is better than 0.2. The effect of blur on tasks of motion and texture perception may reflect the extent to which high spatial frequency information is required for performance on these tasks.

Humans↗
PubMedDate not supplied

Neural models of motion integration and segmentation.

A neural model is developed of how motion integration and segmentation processes compute global motion percepts. Figure-ground properties, such as occlusion, influence which motion signals determine the percept. For visible apertures, a line's extrinsic terminators do not specify true line motion. For invisible apertures, a line's intrinsic terminators create veridical feature tracking signals, which are amplified before they propagate across space and are integrated with ambiguous motion signals within line interiors. This integration process is the result of several processing stages: directional transient cells respond to image transients and input to a directional short-range filter that selectively boosts feature tracking signals. Competitive interactions further boost feature tracking signals and create speed-selective receptive fields. A long-range filter gives rise to true directional cells by pooling signals over multiple orientations and opposite contrast polarities. A distributed population code of speed tuning realizes a size-speed correlation, whereby activations of multiple spatially short-range filters of different sizes are transformed into speed-tuned cell responses. These mechanisms use transient cell responses, output thresholds that covary with filter size, and competition. The model reproduces empirically derived speed discrimination curves and simulates data showing how visual speed perception and discrimination are affected by stimulus contrast.

Models, Neurological↗
PubMed2005

Temporal properties in masking biological motion.

The perception of biological motion using point light animation techniques was investigated in several experiments. Animations simulating walking were presented with additional masking dots. The temporal properties of the walking motion or the temporal relationship between the walking and masking motions were systematically manipulated. Results showed that (1) perception of biological motion was sensitive to even small temporal perturbation within the walker, (2) the effectiveness of a mask depended upon the temporal phase difference between the mask and point light walker, (3) relatively small temporal differences between the mask and point light walker decreased the effectiveness of the mask, and (4) these effects were not due simply to observers detecting the phase offsets in the display. Temporal properties of the motion are important in perceiving the human form in action, just as in other types of figure-ground segregation. This information may be processed by both motion and form pathways for processing biological motion.

Humans↗
PubMed2005

Eccentric perception of biological motion is unscalably poor.

Accurately perceiving the activities of other people is a crucially important social skill of obvious survival value. Human vision is equipped with highly sensitive mechanisms for recognizing activities performed by others [Johansson, G. (1973). Visual perception of biological motion and a model for its analysis. Perception and Psychophysics, 14, 201; Johansson, G. (1976). Spatio-temporal differentiation and integration in visual motion perception: An experimental and theoretical analysis of calculus-like functions in visual data processing. Psychological Research, 38, 379]. One putative functional role of biological motion perception is to register the presence of biological events anywhere within the visual field, not just within central vision. To assess the salience of biological motion throughout the visual field, we compared the detectability performances of biological motion animations imaged in central vision and in peripheral vision. To compensate for the poorer spatial resolution within the periphery, we spatially magnified the motion tokens defining biological motion. Normal and scrambled biological motion sequences were embedded in motion noise and presented in two successively viewed intervals on each trial (2AFC). Subjects indicated which of the two intervals contained normal biological motion. A staircase procedure varied the number of noise dots to produce a criterion level of discrimination performance. For both foveal and peripheral viewing, performance increased but saturated with stimulus size. Foveal and peripheral performance could not be equated by any magnitude of size scaling. Moreover, the inversion effect--superiority of upright over inverted biological motion [Sumi, S. (1984). Upside-down presentation of the Johansson moving light-spot pattern. Perception, 13, 283]--was found only when animations were viewed within the central visual field. Evidently the neural resource responsible for biological motion perception are embodied within neural mechanisms focused on central vision.

Discrimination, Psychological↗
PubMed1987

Model for the extraction of image flow.

A model is presented, consonant with current views regarding the neurophysiology and psychophysics of motion perception, that combines the outputs of a set of spatiotemporal motion-energy filters to extract optical flow. The output velocity is encoded as the peak in a distribution of velocity-tuned units that behave much like cells of the middle temporal area of the primate brain. The model appears to deal with the aperture problem as well as the human visual system since it extracts the correct velocity for patterns that have large differences in contrast at different spatial orientations, and it simulates psychophysical data on the coherence of sine-grating plaid patterns.

Computer Simulation↗
PubMed2002

Middle temporal visual area microstimulation influences veridical judgments of motion direction.

Microstimulation of direction columns in the middle temporal visual area (MT, or V5) provides a powerful tool for probing the relationship between cortical physiology and visual motion perception. In the current study we obtained "veridical" reports of perceived motion from rhesus monkeys by permitting a continuous range of possible responses that mapped isomorphically onto a continuous range of possible motion directions. In contrast to previous studies, therefore, the animals were freed from experimenter-imposed "categories" that typify forced choice tasks. We report three new findings: (1) MT neurons with widely disparate preferred directions can cooperate to shape direction estimates, inconsistent with a pure "winner-take-all" read-out algorithm and consistent with a distributed coding scheme like vector averaging, whereas neurons with nearly opposite preferred directions seem to compete in a manner consistent with the winner-take-all hypothesis, (2) microstimulation can influence direction estimates even when paired with the most powerful motion stimuli available, and (3) microstimulation effects can be elicited when a manual response (instead of our standard oculomotor response) is used to communicate the perceptual report.

Algorithms↗
PubMed1987

Velocity perception and discrimination: relation to temporal mechanisms.

Measurements of three aspects of velocity detection are presented: the upper threshold of motion (UTM), perceived velocity and velocity discrimination. UTM (the highest velocity at which a drifting periodic pattern has the appearance of coherent motion) is reduced by adaptation to a similar drifting pattern of low but not medium or high velocity. The range of adaptation velocities over which the perceived velocity of a test pattern is reduced is quite different, the reduction being greatest at medium adaptation velocities. True velocity discrimination for gratings is possible only at low velocities; at higher velocities other cues (such as temporal frequency) are used. These findings are discussed in relation to current models of motion perception.

Adaptation, Ocular↗
PubMed2006

Multiple sensory cues underlying the perception of translation and path.

The translational linear vestibuloocular reflex compensates most accurately for high frequencies of head translation, with response magnitude decreasing with declining stimulus frequency. However, studies of the perception of translation typically report robust responses even at low frequencies or during prolonged motion. This inconsistency may reflect the incorporation of nondirectional sensory information associated with the vibration and noise that typically accompany translation, into motion perception. We investigated the perception of passive translation in humans while dissociating nondirectional cues from actual head motion. In a cue-dissociation experiment, interaural (IA) motion was generated using either a linear sled, the mechanics of which generated noise and vibration cues that were correlated with the motion profile, or a multiaxis technique that dissociated these cues from actual motion. In a trajectory-shift experiment, IA motion was interrupted by a sudden change in direction (+/-30 degrees diagonal) that produced a change in linear acceleration while maintaining sled speed and therefore mechanical (nondirectional) cues. During multi-axis cue-dissociation trials, subjects reported erroneous translation perceptions that strongly reflected the pattern of nondirectional cues, as opposed to nearly veridical percepts when motion and nondirectional cues coincided. During trajectory-shift trials, subjects' percepts were initially accurate, but erroneous following the direction change. Results suggest that nondirectional cues strongly influence the perception of linear motion, while the utility of cues directly related to translational acceleration is limited. One key implication is that "path integration" likely involves complex mechanisms that depend on nondirectional and contextual self-motion cues in support of limited and transient otolith-dependent acceleration input.

Acceleration↗
PubMed2001

Spatiotemporal visual function in tinted lens wearers.

PURPOSE: Tinted lenses have been widely publicized as a successful new treatment for reading disorders and visual stress in children. The present study was designed to investigate a variety of visual deficits reported by children who experience high levels of visual stress and perceptual distortions when reading (Meares-Irlen syndrome; MIS) and to assess the improvements in visual comfort they report when tinted lenses are worn. METHODS: Twenty children (13.1 +/- 0.9 years of age) were recruited who had successfully worn tinted lenses for at least 6 months and were compared with an age-matched control group (12.6 +/- 2.2 years of age) of 21 children who were not lens wearers. A range of psychophysical tasks was adapted to identify specific anomalous visual perceptions. Spatiotemporal contrast sensitivity and contrast increment thresholds were used to investigate subjective reports of dazzle and hypercontrast, and a minimum motion perception (D(min)) and a motion-coherence task were used to assess subjective reports of visual instability and motion. RESULTS: In all viewing conditions (with versus without lens), no selective functional visual loss was demonstrated with any of the tasks used. Psychometric functions also revealed no significant difference between subject groups (control versus MIS). CONCLUSIONS: Under thorough psychophysical investigation, these results revealed no significant difference in visual function between subject group, and this finding is consistent with the absence of any effect of the tinted lenses in the group with MIS.

Adolescent↗
PubMed1995

Attentional tracking in the perception of apparent motion: evidence from sequential blanking displays.

Perception of sequential blanking displays was studied in a series of three experiments investigating factors that influence whether "shadow motion" or "item motion" is seen in a display. In addition to the duration of the blanking interval (BI) itself, three other such factors were identified: the eccentricity at which the display is viewed, the spacing of items in the display, and the type of motion that subjects are instructed to try to see. It is argued that these and other previously reported results are explicable without the need to invoke any kind of visual integration period. Instead, they are interpreted in terms of a first-order system of automatic luminance detectors and a second-order tracking system involving both voluntary and involuntary attention. The relationship of these findings to other recent work in apparent motion and visual attention and to other bistable motion displays is discussed.

Attention↗
PubMed1994

Properties of the stereoscopic (cyclopean) motion aftereffect.

Across four experiments, this study investigated properties of the stereoscopic motion aftereffect (adaptation from moving retinal disparity information). The results showed that stereoscopic motion can induce an adaptation aftereffect across a wide range of conditions and observers, provided that the duration of adaptation is sufficiently long and a perceptually salient test pattern is viewed. Motion adaptation was found to transfer between the stereoscopic and luminance domains [replicating a previous report by Fox, Patterson and Lehmkuhle (1982) Investigative Ophthalmology and Visual Science (Suppl.), 22, 144], suggesting that motion perception from stereoscopic (second-order) and luminance (first-order) attributes is mediated by a common neural substrate.

Adaptation, Ocular↗
PubMed2005

Specifying the distractor inhibition account of attention-induced motion blindness.

There is growing evidence that motion perception is modulated by visual selective attention. In the 'attention-induced motion blindness' paradigm the detection of coherent motion in a random dot kinematogram (RDK) is impaired in a rapid serial presentation task [Sahraie, A., Milders, M., & Niedeggen, M. (2001). Attention induced motion blindness. Vision Research, 41, 1613-1617]. The effect depends on irrelevant motion episodes (distractors) prior to the target. In this study, we show that both the number and timing of distractors affect detection performance, allowing for implications on the build-up and release of inhibition. Furthermore, we rule out the possibility that subjects falsely classify targets as distractors due to uncertainty of temporal order.

Adult↗