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PubMedDate not supplied

Evaluation of a motion fidelity criterion with visual scene changes.

An experiment examined how visual scene and platform motion variations affected a pilot's ability to perform altitude changes. Pilots controlled a helicopter model in the vertical axis and moved between two points 32-ft apart in a specified time. Four factors were varied: visual-scene spatial frequency, visual-scene background, motion-filter gain, and motion-filter natural frequency. Drawing alternating black and white stripes of varying widths between the two extreme altitude points varied visual-scene spatial frequency. The visual-scene background varied by either drawing the stripes to fill the entire field of view or by placing the stripes on a narrow pole with a natural sky and ground plane behind the pole. Both the motion-filter gain and natural frequency were varied in the motion platform command software. Five pilots evaluated all combinations of the visual and motion variations. The results showed that only the motion-filter natural frequency and visual-scene background affected pilot performance and their subjective ratings. No significant effects of spatial frequency or motion system gain were found for the values examined in this tracking task. A previous motion fidelity criterion was found to still be a reasonable predictor of motion fidelity.

Aerospace Medicine↗
PubMed2005

The relationship between lumbar segmental motion and pain response produced by a posterior-to-anterior force in persons with nonspecific low back pain.

STUDY DESIGN: Cross-sectional. OBJECTIVE: To investigate the association between lumbar segmental motion and pain response during the application of a posterior-to-anterior (PA) force to the lumbar spinous processes in persons with nonspecific low back pain. BACKGROUND: Although low back pain is believed to be associated with altered segmental motion of the lumbar spine, the relationship between subjective reports of pain and objective measurements of segmental motion has not been established. METHODS AND MEASURES: Thirty-five individuals between 18 and 45 years of age with nonspecific low back pain (less than 3 months' duration) participated. All subjects participated in 2 separate procedures: (1) segmental motion assessment during a PA force application over the lumbar spinous processes using dynamic magnetic resonance imaging (MRI), and (2) pain assessment during a PA force application procedure outside of the MRI environment. Frequency counts were used to determine the lumbar segments that were most painful, and which functional spinal units had the most and least motion. Fisher exact tests were performed to determine if an association existed between the most painful segment and the functional spinal unit with the most or least motion. RESULTS: L5 was deemed the most painful segment in nearly half of the participants (48.1%). The L1-2 and L3-4 functional spinal units most frequently had the most motion (25.9% each) and the L4-5 functional spinal units most frequently had the least motion (29.6%). No association was found between the most painful segment and the functional spinal units with either the most or least motion. CONCLUSION: The results of this study indicate that an assumption regarding segmental motion cannot be inferred from the pain response when using a PA force application procedure.

Adolescent↗
PubMed1990

Effects of element orientation on apparent motion perception.

We present an ambiguous motion paradigm that allows us to quantify the influence of aspects of form relevant to the perception of apparent motion. We report on the role of bar element orientation in motion paths. The effect of orientation differences between bar elements in a motion path is small with respect to the crucial role of the orientation of bar elements relative to motion direction. Motion perception between elements oriented along the motion direction dominates motion perception between elements oriented perpendicularly to motion direction. The perception of apparent motion is affected by bar length and width and is anisotropic.

Attention↗
PubMed1989

Auditory apparent motion under binaural and monaural listening conditions.

This investigation examined the ability of listeners to perceive apparent motion under binaural and monaural listening conditions. Fifty-millisecond broadband noise sources were presented through two speakers separated in space by either 10 degrees, 40 degrees, or 160 degrees, centered about the subject's midline. On each trial, the sources were temporally separated by 1 of 12 interstimulus onset intervals (ISOIs). Six listeners were asked to place their experience of these sounds into one of five categories (single sound, simultaneous sounds, continuous motion, broken motion, or successive sounds), and to indicate either the proper temporal sequence of presentation or the direction of motion, depending on whether or not motion was perceived. Each listener was tested at all spatial separations under binaural and monaural listening conditions. Motion was perceived in the binaural listening condition at all spatial separations tested for ISOIs between 20 and 130 msec. In the monaural listening condition, motion was reliably heard by all subjects at 10 degrees and 40 degrees for the same range of ISOIs. At 160 degrees, only 3 of the 6 subjects consistently reported motion. However, when motion was perceived in the monaural condition, the direction of motion could not be determined.

Attention↗
PubMed1990

A comparison of the effects of spatial separation on apparent motion in the auditory and visual modalities.

In the present investigation, the effects of spatial separation on the interstimulus onset intervals (ISOIs) that produce auditory and visual apparent motion were compared. In Experiment 1, subjects were tested on auditory apparent motion. They listened to 50-msec broadband noise pulses that were presented through two speakers separated by one of six different values between 0 degrees and 160 degrees. On each trial, the sounds were temporally separated by 1 of 12 ISOIs from 0 to 500 msec. The subjects were instructed to categorize their perception of the sounds as "single," "simultaneous," "continuous motion," "broken motion," or "succession." They also indicated the proper temporal sequence of each sound pair. In Experiments 2 and 3, subjects were tested on visual apparent motion. Experiment 2 included a range of spatial separations from 6 degrees to 80 degrees; Experiment 3 included separations from .5 degrees to 10 degrees. The same ISOIs were used as in Experiment 1. When the separations were equal, the ISOIs at which auditory apparent motion was perceived were smaller than the values that produced the same experience in vision. Spatial separation affected only visual apparent motion. For separations less than 2 degrees, the ISOIs that produced visual continuous motion were nearly equal to those which produced auditory continuous motion. For larger separations, the ISOIs that produced visual apparent motion increased.

Adult↗
PubMed2004

Congruency effects between auditory and tactile motion: extending the phenomenon of cross-modal dynamic capture.

Behavioral studies of multisensory integration in motion perception have focused on the particular case of visual and auditory signals. Here, we addressed a new case: audition and touch. In Experiment 1, we tested the effects of an apparent motion stream presented in an irrelevant modality (audition or touch) on the perception of apparent motion streams in the other modality (touch or audition, respectively). We found significant congruency effects (lower performance when the direction of motion in the irrelevant modality was incongruent with the direction of the target) for the two possible modality combinations. This congruency effect was asymmetrical, with tactile motion distractors having a stronger influence on auditory motion perception than vice versa In Experiment 2, we used auditory motion targets and tactile motion distractors while participants adopted one of two possible postures: arms uncrossed or arms crossed. The effects of tactile motion on auditory motion judgments were replicated in the arms-uncrossed posture, but they dissipated in the arms-crossed posture. The implications of these results are discussed in light of current findings regarding the representation of tactile and auditory space.

Auditory Perception↗
PubMed1999

Segmentation by color influences responses of motion-sensitive neurons in the cortical middle temporal visual area.

We previously showed that human subjects are better able to discriminate the direction of a motion signal in dynamic noise when the signal is distinguished (segmented) from the noise by color. This finding suggested a hitherto unexplored avenue of interaction between motion and color pathways in the primate visual system. To examine whether chromatic segmentation exerts a similar influence on cortical neurons that contribute to motion direction discrimination, we have now compared the discriminative capacity of single MT neurons and psychophysical observers viewing motion signals with and without chromatic segmentation. All data were obtained from rhesus monkeys trained to discriminate motion direction in dynamic stimuli containing varying proportions of coherently moving (signal) and randomly moving (noise) dots. We obtained psychophysical and neurophysiological data in the same animals, on the same trials, and using the same visual display. Chromatic segmentation of the signal from the noise enhanced both neuronal and psychophysical sensitivity to the motion signal but had a smaller influence on neuronal than on psychophysical sensitivity. Hence the ratio of neuronal to psychophysical thresholds, one measure of the relation between neuronal and psychophysical performance, depended on chromatic segmentation. Increased neuronal sensitivity to chromatically segmented displays stemmed from larger and less noisy responses to motion in the preferred directions of the neurons, suggesting that specialized mechanisms influence responses in the motion pathway when color segments motion signal in visual scenes. These findings lead us to reevaluate potential mechanisms for pooling of MT responses and the role of MT in motion perception.

Animals↗
PubMed2001

Shifts in the population response in the middle temporal visual area parallel perceptual and motor illusions produced by apparent motion.

We recorded behavioral, perceptual, and neural responses to targets that provided apparent visual motion consisting of a sequence of stationary flashes. Increasing the flash separation degrades the quality of motion, but for some separations evoked larger smooth pursuit responses from both humans and monkeys than did smooth motion. The same flash separations also produced an increase in perceived speed in humans. Recordings from single neurons in the middle temporal visual area (MT) of awake monkeys revealed a potential basis for the illusion in the population response. Apparent motion produced diminished neural responses relative to smooth motion. However, neurons with slow preferred speeds were more affected than were those with fast preferred speeds. Increasing the flash separation thus caused the population response to become diminished in amplitude and to shift so that the most active neurons had higher preferred speeds. The entire constellation of effects of apparent motion on the magnitude and latency of the initial pursuit response was accounted for if the MT population response was decoded by (1) creating an opponent motion signal for each neuron by treating its preferred and opposite direction responses as those of a pair of oppositely tuned neurons and (2) computing the vector average of these opponent motion signals. Other ways of decoding the population response recorded in MT failed to account for one or more aspects of behavior. We conclude that the effects of apparent motion on both pursuit and perception can be accounted for if target speed is estimated from the MT population response by a neural computation that implements a vector average based on opponent motion.

Action Potentials↗
PubMed2002

Optokinetic stimuli: motion sickness, visual acuity, and eye movements.

BACKGROUND: It is commonly assumed that motion sickness caused by moving visual scenes arises from the illusion of self-motion (i.e., vection). HYPOTHESES: Both studies reported here investigated whether sickness and vection were correlated. The first study compared sickness and vection created by real and virtual visual displays. The second study investigated whether visual fixation to suppress eye movements affected motion sickness or vection. METHOD: In the first experiment subjects viewed an optokinetic drum and a virtual simulation of the optokinetic drum. The second experiment investigated two conditions on a virtual display: a) moving black and white stripes; and b) moving black and white stripes with a stationary cross on which subjects fixated to reduce eye movements. RESULTS: In the first study, ratings of motion sickness were correlated between the conditions (real and the virtual drum), as were ratings of vection. With both conditions, subjects with poor visual acuity experienced greater sickness. There was no correlation between ratings of vection and ratings of sickness in either condition. In the second study, fixation reduced motion sickness but had no affect on vection. Motion sickness was correlated with visual acuity without fixation, but not with fixation. Again, there was no correlation between vection and motion sickness. CONCLUSIONS: Vection is not the primary cause of sickness with optokinetic stimuli. Vection appears to be influenced by peripheral vision whereas motion sickness is influenced by central vision. When the eyes are free to track moving stimuli, there is an association between visual acuity and motion sickness. Virtual displays can create vection and may be used to investigate visually induced motion sickness.

Adult↗
PubMed2002

Unmasking motion-processing activity in human brain area V5/MT+ mediated by pathways that bypass primary visual cortex.

Most models of the human visual system argue that higher-order motion-processing cortical regions receive their inputs only via the primary visual cortex (striate cortex), rather than also via direct projections from the thalamus that bypass primary visual cortex. However, recent evidence in non-human primates, along with some evidence in humans with damaged primary visual cortex (e.g., "blindsight" for motion in the blind visual hemifield), have argued for the existence of a direct thalamic-to-extrastriate projection for motion processing. This evidence remains controversial. Here we tested the idea that direct thalamic input to extrastriate motion processing areas exists in humans but might be masked in scalp recordings by activity from early visual areas. To do this, we employed stimuli that induced strong refractory effects in primary visual cortex--thereby creating a brief "reversable lesion" in primary visual cortex--immediately before the presentation of a motion stimulus. Under these conditions, we then assessed whether motion areas of cortex were still able to process the motion stimuli by recording event-related potentials (ERPs) and event-related magnetic fields (ERFs/MEG). We found robust motion-related activity in extrastriate motion processing areas in the ERP and MEG signals even when primary visual cortex was heavily suppressed by our manipulation. This finding provides evidence for a direct thalamic functional pathway to extrastriate visual cortical motion processing areas in the human that bypasses primary visual cortex.

Adult↗
PubMed2006

Perceived self-motion in two visual contexts: dissociable mechanisms underlie perception.

We evaluated the influence of moving visual scenes and knowledge of spatial and physical context on visually induced self-motion perception in an immersive virtual environment. A sinusoidal, vertically oscillating visual stimulus induced perceptions of self-motion that matched changes in visual acceleration. Subjects reported peaks of perceived self-motion in synchrony with peaks of visual acceleration and opposite in direction to visual scene motion. Spatial context was manipulated by testing subjects in the environment that matched the room in the visual scene or by testing them in a separate chamber. Physical context was manipulated by testing the subject while seated in a stable, earth-fixed desk chair or in an apparatus capable of large linear motions, however, in both conditions no actual motion occurred. The compellingness of perceived self-motion was increased significantly when the spatial context matched the visual input and actual body displacement was possible, however, the latency and amplitude of perceived self-motion were unaffected by the spatial or physical context. We propose that two dissociable processes are involved in self-motion perception: one process, primarily driven by visual input, affects vection latency and path integration, the other process, receiving cognitive input, drives the compellingness of perceived self-motion.

Adolescent↗
PubMed2007

[Parallel processing of motion vision].

Several neuropsychological studies have reported dissociation between motion vision and object vision. One patient with motion blindness had a bilateral MT/V5 lesion and could see objects, but could not see the motion of the objects (Zihl et al, 1983). By contrast, some blindsight patients with primary visual cortex lesions cannot see objects but can see their movement (e.g. Riddoch, 1917). These results imply that movement vision and form vision rely on independent mechanisms. However one patient with motion blindness had controversial symptoms concerning motion vision. She could not perceive the movement of objects, although she could walk without colliding with obstacles and could catch incoming objects. It has also been reported that patients with a bilateral parietal lesion had well-preserved primary motion vision, but had problems walking and catching a ball (Vaina, 1998). Therefore, motion for vision and motion for action might have independent mechanisms. Such dissociation has also been noted in patients with Bálint syndrome. Some patients behave like a blind person but can walk and catch a ball, while other patients bump into obstacles while walking. These results indicate that the neural bases of motion vision are distinct from those of form vision and that there are subdivisions of motion vision.

Agnosia↗
PubMed1994

Continuous passive motion stimulates repair of rabbit knee articular cartilage after matrix proteoglycan loss.

Continuous passive motion facilitates repair of full-thickness defects in the articular cartilage in rabbits. Studies were conducted to determine whether continuous passive motion would similarly affect the repair process after injection of chymopapain into the rabbit knee. Adolescent rabbits were injected with chymopapain and then given intermittent active motion in the form of free cage activity or continuous passive motion of the injected knee. After injection of either 0.2 or 2 mg chymopapain into the knee, serum keratan sulfate levels rose sharply, indicating proteoglycan loss, and, in all cases, peaked at 24 hours between 200-800% of preinjection levels. Importantly, serum keratan sulfate levels were significantly elevated within 1 hour when joints were submitted to immediate continuous passive motion after the injection. As shown previously, injection of either 0.2 or 2 mg chymopapain into the knee, followed by intermittent active motion, resulted in a pronounced loss of proteoglycans by Day 2, partial restoration of proteoglycans by Day 9, continued proteoglycan synthesis by Day 21 in animals receiving the lower dose, and severe degenerative changes by Day 21 in animals receiving the higher dose. In all animals that received either high or low doses of chymopapain, as well as 2 days of intermittent active motion and then continuous passive motion, the articular cartilage surface was intact by Day 9, and replenishment of proteoglycans had occurred in pericellular and interterritorial areas. By Day 21, the surface of the articular cartilage was still intact, and replenishment of proteoglycans in loaded regions continued in all animals receiving either dose of chymopapain. These results indicate that a period of intermittent active motion followed by continuous passive motion of a chymopapain injected knee may protect and stimulate repair of the articular cartilage matrix after chymopapain-induced injury.

Animals↗
PubMed1993

Effect of motion on thallium-201 SPECT studies: a simulation and clinical study.

Although patient motion on 201Tl SPECT studies has been reported as a source of artifacts, systematic studies on motion patterns and resultant artifacts are lacking. Accordingly, we simulated 74 motion patterns upon a normal study. The tomograms were assessed for presence of defects: The "motion pixel area index" ranged from 1 to 83; 26 of 30 (87%) simulations with an index > or = 21 had defects, whereas 38 of 44 (86%) simulations with an index < 21 were normal. Defect location was dependent on motion direction; defect intensity was dependent on its magnitude and timing. Review of data acquisition in 164 recent normal patient studies revealed motion in 42 (26%). Motion was generally minimal and caused defects in only seven (4%). Thus, mild motion is unlikely to produce defects. In our laboratory, motion is now an infrequent source of artifacts; severe motion produces recognizable patterns that depend on its direction, magnitude and timing.

Adult↗
PubMed1993

Passive motion: the dose effects on joint stiffness, muscle mass, bone density, and regional swelling. A study in an experimental model following intra-articular injury.

We studied the effects of passive motion on joint stiffness, muscle mass, bone density, and regional swelling after an intra-articular injury. Instrumentation was applied to the hindlimbs of thirty adolescent New Zealand White rabbits to allow either passive motion or immobilization of the ankle. The knee was immobilized by the locking together of Steinmann pins that had been placed within the medullary canals of the tibia and femur. An intra-articular injury was produced by drilling of the tibial pin through the ankle joint into the talus and subsequent withdrawal of the pin from the ankle joint. The rabbits were divided into five groups, and they received four, eight, twelve, sixteen, or twenty-four hours of passive motion each day during the three-week period of study. One ankle of each rabbit was moved through an arc of 90 to 170 degrees of dorsiflexion at one cycle per minute, while the contralateral ankle was immobilized in 100 degrees of dorsiflexion with an aluminum splint, which was fixed to the aluminum block that was used to stabilize the knee joint. We found that sixteen and twenty-four hours of passive motion prevented stiffness of the joint. Passive motion for shorter periods was ineffective, even harmful, and resulted in stiffness ratios that were as much as four times higher than those of the control limbs (those treated with immobilization). Swelling of the limb decreased only in the group that received twenty-four hours of passive motion. Muscle mass increased by an average of 13 per cent (range, 4 to 34 per cent), in comparison with that of the immobilized limbs in every group that was treated with passive motion. Bone density was maintained only in the limbs in which the ankle became stiff (ankles that had been treated with passive motion for twelve hours or less). An inverse relationship was noted between the duration of passive motion and the radiographic density of the distal tibial metaphysis; this relationship was statistically significant (p < 0.01). The limbs treated for twelve, eight, or four hours each day showed progressively greater bone density in comparison with those treated with immobilization or with sixteen or twenty-four hours of passive motion.

Animals↗
PubMed1993

Dynamic visual acuity of normal subjects during vertical optotype and head motion.

PURPOSE: To characterize the effect of passive vertical head motion on dynamic visual acuity of young, normally sighted subjects wearing telescopic spectacles, and to relate this to the velocity of images on the retina. METHODS: Static visual acuity was measured without motion. Dynamic visual acuity was measured during vertical, sinusoidal motion of either optotypes or of a servo-driven rotating chair in which subjects were seated. Dynamic visual acuity for head motion was measured unaided, as well as with 1.9X, 4X, and 6X telescopic spectacles. Vertical eye movements were recorded using magnetic search coils. RESULTS: During optotype motion, acuity declined with increasing velocity to a minimum of approximately 20/200 at 100 degrees/sec. Pursuit gain (eye velocity/optotype velocity) for moving optotypes was low except for optotype velocities of 20 degrees/sec of less. Dynamic visual acuity without telescopic spectacles was not sensitive to head motion. Static visual acuity improved with increasing telescopic spectacle power, but dynamic visual acuity became progressively impaired by head motion as telescopic spectacle power was increased. Compared with static visual acuity, head motion with peak velocity of 40 degrees/sec reduced acuity two-fold for 1.9X telescopic spectacles, fourfold for 4X telescopic spectacles, and eightfold for 6X telescopic spectacles. Visual vestibulo-ocular reflex gain with telescopic spectacles increased to values markedly above 1.0, but was always less than telescopic spectacle magnification. There was visual tolerance of slip velocities of 2 degrees/sec or less, above which acuity declined in proportion to the 0.6 power of retinal slip velocity. Above 2 degrees/sec, retinal slip velocity accounted for 95% of the variance in dynamic visual acuity. CONCLUSIONS: These results confirm that acuity is sensitive to retinal image motion in the vertical direction, and extend this finding to indicate that sensitivity of acuity to vertical head motion during wearing of telescopic spectacles is attributable to retinal image slip velocity.

Adult↗
PubMed1996

Effect of frequency of horizontal linear oscillation on motion sickness and somatogravic illusion.

BACKGROUND: Low frequency linear (translational) oscillation is an important stimulus in provoking motion sickness in a variety of modes of transport. HYPOTHESIS: Lower frequencies of horizontal linear oscillation would be more nauseogenic. The somatogravic illusion (SGI) would be affected by frequency. METHODS: Subjects (n = 12) were exposed to horizontal sinusoidal motion (3.6 m.s-2 peak) at three different frequencies (0.205 Hz, 0.350 Hz, 0.500 Hz) at one week intervals, with order randomized between subjects. Subjects were seated in the upright position, with motion through the X head body axis. RESULTS: The mean (+/- S.D.) motion exposure time required to produce moderate nausea decreased significantly (p < 0.01) towards the lower frequency: 24.4 +/- 19.3 min. at 0.500 Hz, 12.0 +/- 9.5 min. at 0.350 Hz, 7.8 +/- 6.2 min. at 0.205 Hz. The linear fit of time (t) to nausea with frequency was -7.4 dB/octave. This was equivalent to a -3.7 dB/octave decrease of nauseogenic potential with increasing frequency, if t1/2 were to be used as in the standard "motion dose" models. The SGI was reported by 5/12 subjects (mean illusory tilting angles 16.2 degrees forward, 14.3 degrees back) but there was no relationship between SGI and motion frequency or motion sickness. CONCLUSIONS: Horizontal motion with subjects seated upright was more nauseogenic than would be predicted by mathematical models based on vertical oscillation, and the relationship of frequency to nauseogenicity for horizontal motion was significantly less steep than that previously reported for vertical motion.

Adult↗
PubMed1998

Anomalies of motion perception in infantile esotropia.

PURPOSE: To quantify motion sensitivity in patients with infantile esotropia who, as a subgroup, have been previously reported to have abnormal oculomotor control. In addition, to probe abnormal binocular development as a factor underlying abnormal motion perception in infantile esotropia (IE), motion sensitivity was compared among participants with and without stereopsis. METHODS: Monocular sensitivity to leftward and rightward motion was assessed across the horizontal meridian, using partially coherent random dot kinematograms. Participants included 11 observers with IE, 5 observers with acquired esotropia, and 11 observers with normal eye alignment. RESULTS: Participants with IE showed no deficits in motion sensitivity to any visual field locations when motion thresholds were collapsed across direction. However, they showed an abnormal variation in directional anisotropy. Although sensitivity to centripetal motion was superior in both hemifields of control participants and in the temporal hemifields of participants with IE, a centrifugal bias was revealed in the nasal hemifields of IE. Stereoblind observers with acquired esotropia showed a normal centripetal directional anisotropy, whereas binocular observers with acquired esotropia showed directional anisotropy similar to that in the IE group. CONCLUSIONS: Motion perception, like oculomotor function in IE, is characterized by a variation of directional anisotropy for stimuli presented to the nasal hemifields. This finding supports the hypothesis that abnormal oculomotor control and motion perception in IE reflect a common disruption of the visual system. A similar variation of directional sensitivity in patients with acquired esotropia with normal stereopsis suggests that the interruption of binocularity is not the underlying cause of abnormal motion perception in IE.

Adolescent↗