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PubMed1994

Global motion perception: interaction of the ON and OFF pathways.

A number of experiments were conducted to investigate the interaction of the ON and OFF pathways in the processing of global-motion signals. The stimulus employed was a variant of that used by Newsome and Pare [(1988) Journal of Neuroscience, 8, 2201-2211] in which a small subset of dots move in a common (global-motion) direction in a field of randomly moving dots. The threshold measure was the number of dots required to move in the global-motion direction for that direction to be detected. We found that: (1) the extraction of a global-motion signal carried by light dots (luminance above the background) was impaired by the addition of dark dots (luminance below the background) which did not carry the signal (noise dots); (2) sub-threshold summation occurs for global-motion signals carried by light and dark dots; and (3) a signal dot which changed luminance polarity (went from light to dark) did not result in a motion signal--either in the global-motion direction or in the opposite direction (reverse apparent motion). From these findings we conclude that the inputs to the motion sensitive cells have matched spatial opponency (the ON and OFF pathways remain separate at this level) but that they then combine to form a single pathway prior to the extraction of the global-motion signal. These findings are contrary to those predicted by models which advocate squaring or full-wave rectification prior to global motion processing.

Contrast Sensitivity↗
PubMed1979

Space motion sickness.

Space motion sickness, presumably triggered by sudden entry into a weightless environment, occurred with unexpected frequency and severity among astronauts who flew the Skylab missions. Recovery from symptoms was complete within 3-5 days, and as revealed by the Skylab M131 Human Vestibular Function Experiment, all crewmembers were immune to experimentally induced motion sickness after mission day 8. This syndrome has been recognized as a possible threat to the early mission well-being and operational efficiency of at least some individuals who will fly space missions in the future. The causes of space motion sickness are not clearly understood, nor have satisfactory methods been identified to date for its prediction, prevention and treatment. In order to minimize the potential impact of this syndrome on Space Shuttle crew operations the National Aeronautics and Space Administration has organized a broad program of inter-disciplinary research involving a large number of scientists in the United States. Current research on the etiology of space motion sickness is based to a large extent on the so called sensory conflict theory. Investigations of the behavioral and neurophysiological consequences of intralabyrinthine, as well as intermodality sensory conflict are being performed. The work in this area is being influenced by the presumed alterations that occur in otolith behavior in weightlessness. In addition to sensory conflict, the possible relationship between observed cephalad shifts of body fluids in weightlessness and space motion sickness is being investigated. Research to date has failed to support the fluid shift theory. Research underway to identify reliable test methods for the prediction of susceptibility to space motion sickness on an individual basis includes attempts to (a) correlate susceptibility in different provocative environments; (b) correlate susceptibility with vestibular and non-vestibular response parameters, the latter including behavioral, hemodynamic and biochemical factors and (c) correlate susceptibility with rate of acquisition and length of retention of sensory adaptation. Controlled studies are also being performed during parabolic flight as a means of attempting to validate predictive tests for susceptibility to this syndrome. Research to develop new or improved countermeasures for space motion sickness is underway in two primary areas. One of these involves anti-motion sickness drugs. Significant achievements have been realized with regard to the identification of new highly efficacious drug combinations, dose levels and routes of administration. Although pronounced individual variations must be accounted for in selecting the optimum drug and dose level, combinations of promethazine plus ephedrine or scopolamine plus dexidrine are presently the drugs of choice. Work is also underway to identify side effects associated with anti-motion sickness drug use and to identify new drugs which may selectively modify activity in central neural pathways involved in motion sickness. In addition to research on drugs, efforts are being made to develop practical vestibular training methods. Variables which influence rate of acquisition of adaptation, length of retention of adaptation and transfer of protective adaptation to new environments are being evaluated. Also, included in this area is the use of biofeedback and autogenic therapy to train individuals to regulate autonomic responses associated with motion sickness. While valuable new knowledge is expected to evolve from these combined research programs, it is concluded that the final validation of predictive tests and countermeasures will require a series of controlled space flight experiments.

Adaptation, Physiological↗
PubMed2006

Three-dimensional in vivo motion of adult hind foot bones.

Knowledge of hind foot bone motion is important for understanding gait as well as various foot pathologies, but the three-dimensional (3D) motion of these bones remains incompletely understood. The purpose of this study was to quantify the motion of the talus, calcaneus, navicular, and cuboid in normal adult feet during open chain quasi-static uniplanar plantar flexion motion. Magnetic resonance images of the right feet of six normal young adult males were taken from which 3D virtual models were made of each hind foot bone. The 3D motion of these models was analyzed. Each hind foot bone rotated in the same plane about half as much as the foot (mean 0.54 degrees of bone rotation per degree of foot motion, range 0.40-0.73 degrees per degree of foot motion as measured relative to the fixed tibia). Talar motion was primarily uniaxial, but the calcaneus, navicular, and cuboid bones exhibited biplanar (sometimes triplanar) translation in addition to biaxial rotation. Net translational motions of these bones averaged 0.39 mm of bone translation per degree of foot motion (range 0.06-0.62 mm per degree of foot motion). These data reflect the functional anatomy of the foot, extend the findings of prior studies, provide a standard for comparison to patients with congenital or acquired foot deformities, and establish an objective reference for quantitatively assessing the efficacy of various hind foot therapies.

Adolescent↗
PubMed2005

Impaired visual recognition of biological motion in schizophrenia.

BACKGROUND: Motion perception deficits have been suggested to be an important feature of schizophrenia but the behavioral consequences of such deficits are unknown. Biological motion refers to the movements generated by living beings. The human visual system rapidly and effortlessly detects and extracts socially relevant information from biological motion. A deficit in biological motion perception may have significant consequences for detecting and interpreting social information. METHODS: Schizophrenia patients and matched healthy controls were tested on two visual tasks: recognition of human activity portrayed in point-light animations (biological motion task) and a perceptual control task involving detection of a grouped figure against the background noise (global-form task). Both tasks required detection of a global form against background noise but only the biological motion task required the extraction of motion-related information. RESULTS: Schizophrenia patients performed as well as the controls in the global-form task, but were significantly impaired on the biological motion task. In addition, deficits in biological motion perception correlated with impaired social functioning as measured by the Zigler social competence scale [Zigler, E., Levine, J. (1981). Premorbid competence in schizophrenia: what is being measured? Journal of Consulting and Clinical Psychology, 49, 96-105.]. CONCLUSION: The deficit in biological motion processing, which may be related to the previously documented deficit in global motion processing, could contribute to abnormal social functioning in schizophrenia.

Adult↗
PubMed2004

Components of motion perception revealed: two different after-effects from a single moving object.

If motion that one has been looking at for some time suddenly stops, or if one shifts one's gaze to a static object, one will see motion in the opposite direction: the motion after-effect. If two transparent surfaces move with different speeds in different directions, then the direction of the motion after-effect will depend on the test pattern. For such transparent surfaces both the local motion and the global percept have two components. When looking at a normal moving object, there is only one perceived global motion. However, we know that locally there can be considerable ambiguity (the aperture problem). Does one adapt to all the local components, including those that one does not perceive, or only to the perceived global motion? We designed a stimulus that is perceived to be a fast rotating object, but also has a slow local radial component of motion. By selecting an appropriate test pattern we could either get a radial or a rotating motion after-effect. Thus we show that adaptation to motion must (also) occur at a stage at which local motions have not yet been integrated to give a unified percept.

Adaptation, Physiological↗
PubMed2005

Motion detection in normal infants and young patients with infantile esotropia.

The purpose of this study was to investigate asymmetries in detection of horizontal motion in normal infants and children and in patients with infantile esotropia. Motion detection thresholds (% motion signal) were measured in 75 normal infants and in 36 eyes of 27 infants with infantile esotropia (ET), using a forced-choice preferential looking paradigm with random-dot patterns. Absolute motion detection sensitivity and asymmetries in sensitivity for nasalward (N) vs. temporalward (T) directions of motion were compared in normal and patient populations, ranging in age from 1 month to 5 years. In normal infants, N and T thresholds were equivalent under 2.5 months of age, whereas a superiority for monocular detection of N motion was observed between 3.5 and 6.5 months of age. The nasalward advantage gradually diminished to symmetrical T:N performance by 8 months of age, matching that of adults. No asymmetry was observed in 15 normal infants who performed the task binocularly, hence, the asymmetry was not a leftward/rightward bias. In the youngest infantile ET patients tested, at 5 months of age, a nasalward superiority in motion detection was observed and was equivalent to that of same-age normal infants. However, unlike normals, this asymmetry persists in older patients. This greater asymmetry in infantile ET represents worse detection of T than N motion. This is the first report of an asymmetry in motion detection in normal infants across a wide age range. Initially, motion detection is normal in infants with infantile esotropia. Cumulative abnormal binocular experience in these patients may disrupt motion mechanisms.

Aging↗
PubMed2003

Ranking systems for evaluation of joint and joint motion stressfulness based on perceived discomforts.

This study aims to develop ranking systems for evaluation of the stressfulness of joints and joint motions based on perceived discomforts measured through an experiment. Twenty healthy male subjects participated in the experiment, where discomforts for varying joint motions in the sitting and standing postures were measured using the magnitude estimation. The results showed that the perceived discomforts were affected by the type of joint motions, size of joint motions, and joints. The joints and joint motions were classified into several distinct classes according to perceived stresses. Three ranking systems based on the perceived discomforts were developed, including classification by the joint motions and joints, by types of joint motions, and by the joints only. The ranking systems revealed that while hip and back motions exhibited higher discomfort ratings than any other joint motion, elbow motions were the least stressful of all joint motions. The ranking systems can be used as a valuable design guideline when ergonomically designing or evaluating workplaces, or as a helpful tool for understanding adverse effects of poor working postures.

Adult↗
PubMed1999

The role of motion in children's categorization of objects.

Perceptual cues play a fundamental role in early categorization of objects. What is meant by perceptual cues in the literature, however, is not always clear. It is fair to say that they are typically understood to be static shape cues. A number of recent studies have suggested that dynamic perceptual cues, such as motion, may also be important in early categorization. The study presented here explored the role that motion plays in children's categorization of animal and non-animal kinds, such as geometric figures. Motion was directly pitted against shape as a cue for categorization. Results showed that 4-year-old children, confronted with a choice between shape and motion, significantly used motion cues over shape cues to categorize objects, regardless of whether they were animals or geometric figures. Seven-year-olds also tended to use motion more often to categorize animals but not when dealing with geometric figures. Older children, who have been found to have a clearer natural kind/artifact distinction, seem to appreciate the uniqueness of movement to animals and see motion as more relevant to their categorization but relatively less so to categorize geometric figures. This developmental shift in the categorization of animals and geometric figures based on motion was further confirmed by testing adults on the same tasks. Adults were found to base their judgements significantly more often on motion for animals but not for geometric figures. These findings support the view that children are initially guided by motion in object categorization, suggesting that motion plays an overriding role that is central in the process of concept acquisition and in the mechanisms by which concepts are later structured.

Analysis of Variance↗
PubMed2000

Visual motion detection in man is governed by non-retinal mechanisms.

It is generally assumed that there is no sizable proportion of motion detectors in the primate retina. To test this specifically for humans, visual evoked potentials (VEPs) and electroretinograms (ERGs) were recorded simultaneously to visual motion onset (9.3 degrees /s) of an expanding or contracting 'dartboard'. The degree of motion-specific responses in cortex and retina was assessed by testing the direction specificity of motion adaptation with three conditions in a fully balanced paradigm: motion-onset potentials were measured after adaptation to: (1) a stationary pattern; (2) motion in the same direction as the test stimulus; and (3) motion in the opposite direction. Motion-onset responses in the VEP were dominated by the typical N2 at 150 ms, in the ERG by a positivity at 70 ms. Onset of contraction or expansion evoked virtually identical VEP and ERG responses (P>0.5). Motion adaptation produced strong direction-specific effects in the VEP (P<0.05), but not in the ERG (P=0.58): In the adapting and non-adapting direction the VEP (N2) was reduced by 75 and 50% (P<0.001), the ERG by 32 and 26% (P<0.01 and 0.05), respectively. The striking difference of the direction-specificity of motion adaptation between cortex and retina suggests that in humans the vast majority of motion-specific processing occurs beyond the retinal ganglion cells.

Electroretinography↗
PubMed2001

Sensitive calibration and measurement procedures based on the amplification principle in motion perception.

We compare two types of sampled motion stimuli: ordinary periodic displays with modulation amplitude m(o=e) that translate 90 degrees between successive frames and amplifier sandwich displays. In sandwich displays, even-numbered frames are of one type, odd-numbered frames are of the same or different type, and (1) both types have the same period, (2) translate in a consistent direction 90 degrees between frames, and (3) even frames have modulation amplitude m(e), odd frames have modulation amplitude m(o). In both first-order motion (van Santen, J.P.H. & Sperling, G. (1984). Temporal covariance model of human motion perception. Journal of the Optical Society of America A, 1, 451-73) and second-order motion (Werkhoven, P., Sperling, G., & Chubb, C. (1993). Motion perception between dissimilar gratings: a single channel theory. Vision Research, 33, 463-85) the motion strength of amplifier sandwich displays is proportional to the product m(o)m(e) for a wide range of m(e). By setting m(e) to a large value, an amplifier sandwich stimulus with a very small value of m(o) can still produce visible motion. The amplification factor is the ratio of two threshold modulation amplitudes: ordinary circumflexm(o=e) over amplified circumflexm(o), circumflexm(o=e)/circumflexm(o). We find amplification factors of up to about 8x. Light adaptation and contrast gain control in early visual processing distort the representations of visual stimuli so that inputs to subsequent perceptual processes contain undesired distortion products or 'impurities'. Motion amplification is used to measure and thence to reduce these unwanted components in a stimulus to a small fraction of their threshold. Such stimuli are certifiably pure in the sense that the residual impurity is less than a specified value. Six applications are considered: (1) removing (first-order) luminance contamination from moving (second-order) texture gratings; (2) removing luminance contamination from moving chromatic gratings to produce pure isoluminant gratings; (3) removing distortion products in luminance-modulated (first-order) gratings - by iterative application, all significant distortion products can be removed; (4) removing second-order texture contamination from third-order motion displays; (5) removing feature bias from third-order motion displays; (6) and the same general principles are applied to texture-slant discrimination in which x,y spatial coordinates replace the x,t motion coordinates. In all applicable domains, the amplification principle provides a powerful assay method for the precise measurement of very weak stimuli, and thereby a means of producing visual displays of certifiable purity.

Adaptation, Ocular↗
PubMed1997

Motion minima for different directions in color space.

We have used the minimum-motion stimulus of Cavanagh, MacLeod & Anstis [(1987) Journal of the Optical Society of America A, 4, 1428-1438] to examine how signals along different directions in color space interact in motion perception. Stimuli were pairs of counterphasing gratings combined 90 deg out of phase in both space and time and modulated along different color-luminance axes. The axis for one of the gratings was fixed, while the axis for the second was varied so as to null perceived motion in the stimulus. The motion nulls show that observers are sensitive to motion signals carried by each of the cardinal directions of color space [an achromatic axis and L-M and S-(L+M) chromatic axes], but that signals along different cardinal axes are not combined to yield a net direction of motion. Pairing an achromatic and chromatic grating resulted in a motion null regardless of the relative or overall contrast of the two gratings, while the null directions for intermediate axes shifted depending on contrast. This result points to the special status of the luminance and chromatic axes. However, our results do not reveal a special pair of axes within the equiluminant plane. When contrasts along the cardinal axes are scaled for equal multiples of their respective detection thresholds, the L-M and S chromatic contrasts contribute roughly equally to the perceived motion, but are many times weaker than luminance contrast. Moreover, sensitivity to luminance motion is little affected by the presence of chromatic contrast, whereas sensitivity to chromatic motion is strongly masked by either luminance or chromatic contrast. These asymmetric interactions suggest that the motion of the luminance and chromatic components is encoded in qualitatively different ways.

Color Perception↗
PubMed1997

Direction discrimination of cyclopean (stereoscopic) and luminance motion.

This study compared direction discrimination of cyclopean (stereoscopic) and luminance motion involving stimuli equated for effective strength. The stimuli were random-walk cinematogram (RWC) displays whose signal and noise discs were created from binocular disparity differences embedded in a dynamic random-dot stereogram or from luminance differences. Experiment 1 measured global motion detection thresholds for cyclopean and luminance stimuli by manipulating the proportion of signal to noise discs. Detection thresholds for cyclopean motion were about 25% whereas detection thresholds for luminance motion were 5%, thus five times more cyclopean motion events than luminance events were necessary to elicit threshold responding. Experiment 2 measured thresholds for discriminating the direction of cyclopean and luminance motion under conditions of equal stimulus strength by presenting the motion displays at equal multiples of detection threshold. Direction discrimination thresholds (ranging from about 5-30 deg, depending upon conditions) were similar for cyclopean and luminance motion, thus the precision with which the pooling of local motion events in one direction can be discriminated from the pooling of events in a slightly different direction is the same for cyclopean and luminance stimuli. The finding that cyclopean motion information is pooled is consistent with the idea that the direction of cyclopean motion is coded in the responses of a population of directionally selective mechanisms.

Depth Perception↗
PubMed1998

Interactions between global motion and local binocular rivalry.

Binocular rivalry is thought to arise from a low-level cortical site. Experiment 1 evaluates this claim with respect to local and global motion processing by using a multiple-aperture motion stimulus and measuring the predominance of global coherence while one of the component gratings is engaged in rivalry. Results show that rivalry suppression of the component grating precludes global coherence. Presumable, suppression prevents the component motion signal from advancing to higher-level global motion areas, suggesting rivalry occurs between local and global motion processing. However, feedback from higher-level mechanisms might exert an influence on binocular rivalry and thus Experiment 2 measures how the predominance of a local target engaged in binocular rivalry with a competing local stimulus is affected when the target forms part of a globally coherent motion stimulus. The augmented level of target predominance during global motion relative to local motion indicates that higher-level motion mechanisms can feedback and influence the binocular rivalry process. Together, these data imply a looping hierarchy of motion processing stages, with rivalry suppression transpiring at an intermediate level and subject to feedback from higher-level motion areas.

Humans↗
PubMed1998

Global induced motion and visual stability in an optic flow illusion.

When an expansion flow field of moving dots is overlapped by planar motion, observers perceive an illusory displacement of the focus of expansion (FOE) in the direction of the planar motion (Duffy and Wurtz, Vision Research, 1993;33:1481-1490). The illusion may be a consequence of induced motion, wherein an induced component of motion relative to planar dots is added to the motions of expansion dots to produce the FOE shift. While such a process could be mediated by local 'center-surround' receptive fields, the effect could also be due to a higher level process which detects and subtracts large-field planar motion from the flow field. We probed the mechanisms underlying this illusion by adding varying amounts of rotation to the expansion stimulus, and by varying the speed and size of the planar motion field. The introduction of rotation into the stimulus produces an illusory shift in a direction perpendicular to the planar motion. Larger FOE shifts were perceived for greater speeds and sizes of planar motion fields, although the speed effect saturated at high speeds. While the illusion appears to share a common mechanism with center-surround induced motion, our results also point to involvement of a more global mechanism that subtracts coherent planar motion from the flow field. Such a process might help to maintain visual stability during eye movements.

Cues↗
PubMed1998

Position displacement, not velocity, is the cue to motion detection of second-order stimuli.

Motion detection can be achieved either with mechanisms sensitive to a target's velocity, or sensitive to change in a target's position. Using a procedure to dissociate these two provided by Nakayama and Tyler (Vis Res 1981;21:427-433), we explored detection of first-order (luminance-based) and various second-order (texture-based and stereo-based) motion. In the first experiment, observers viewed annular gratings oscillating in rotational motion at various rates. For each oscillation temporal frequency, we determined the minimum displacement of the pattern for which observers could reliably see motion. For first-order motion, these motion detection thresholds decreased with increasing temporal frequency, and thus were determined by a minimum velocity. In contrast, motion detection thresholds for second-order motion remained roughly constant across temporal frequency, and thus were determined by a minimum displacement. In Experiment 2, luminance-based gratings of different contrasts were tested to show that the velocity-dependence was not an artifact of pattern visibility. In the remaining experiments, results similar to Experiment 1 were obtained with a central presentation of a linear grating, instead of an annular grating (Experiment 3), and with a motion discrimination (phase discrimination) rather than motion detection task (Experiment 4). We conclude that, within the ranges tested here, second-order motion is more readily detected with a mechanism which tracks the change of position of features over time.

Contrast Sensitivity↗
PubMed2000

Tracking the apparent location of targets in interpolated motion.

Under appropriate conditions, a target moving in discrete steps can appear to move smoothly and continuously even within the portions of the path where no physical stimulus is present. We investigated the nature of this interpolated motion in attentive tracking displays as well as apparent motion. The results showed that the apparent location of the target moved smoothly through space between the two discrete locations and the judgements of interpolated motion for attentive tracking and apparent motion were comparable to those for continuous motion in both the perceived path and the precision of the judgements. There were few, if any, differences between judgements for real and interpolated motion. An alignment procedure showed that the smooth change in location judgements was real and not a consequence of averaging across discrete locations actually seen on each trial. We also found that the slowest alternation rate which supported accurate location judgements corresponded to a critical SOA of about 500 ms, similar to the longest SOA which supported a subjective impression of motion in the display. Deviations from a constant velocity which were shorter than 200 ms did not register in the judged motion path, suggesting a fairly long time constant for the integration of velocity information into the perceived motion. These results suggest a specialized motion analysis which provides an accurate, explicit model of the interpolated motion path.

Attention↗
PubMed1997

Alterations in R-R variability associated with experimental motion sickness.

Motion sickness is a complex integration of responses from multiple physiological systems. Whether the changes that occur during the time course of motion sickness are mediated by the sympathetic or parasympathetic systems is still controversial. The present study evaluates alterations in R-R variability during experimental motion sickness in motion sick and non-motion sick subjects. Ten motion sick subjects and 7 non-motion sick subjects participated in the study. Power spectrum analysis of R-R variation was conducted for all subjects 10 min before a brief vestibular disorientation test (BVDT), for 5-10 min of the test, and 10 min after the test. Subjects were also asked to report their symptoms during the test. The motion sick group showed a significant reduction in the power spectrum density of the R-R interval at the mid and high frequencies during the BVDT test period (BVDT), in comparison with the rest period (Rest). These changes probably indicate a decrease in parasympathetic activity during the time course of motion sickness. The non-motion sick group did not show significant differences at any of the frequencies during BVDT. Power spectrum analysis of the R-R interval provides an objective measure of the autonomic response to experimental motion sickness.

Adolescent↗
PubMed1999

Normal global motion of the cervical spine: an electrogoniometric study.

OBJECTIVE: Establishment of a normal database and clinical reference of active global cervical spine motion ranges and patterns using a commercial electrogoniometer. DESIGN: Three-dimensional cervical motion ranges and patterns were analyzed in 250 asymptomatic volunteers. BACKGROUND: In vivo out-of-plane motion patterns of the cervical spine have not yet been reported in large populations, but could be of clinical interest. METHODS: In 250 subjects (aged 14-70 yr), motion range and patterns between the first thoracic vertebra and the head were analyzed for flexion-extension, lateral bending, rotation in neutral sagittal plane position and in full flexion using the CA 6000 Spine Motion Analyzer. RESULTS AND CONCLUSIONS: Average motion range in the sagittal plane was 122 degrees (SD: 18 degrees ). Flexion was slightly more important than extension. Out-of-plane components were negligible. Global bending range averaged 88 degrees (SD: 16 degrees ), left and right bending being comparable. Homolateral rotation was associated to lateral bending. Its extent was approximately 40% of the bending range. Global rotation range in neutral sagittal plane position was 144 degrees (SD: 20 degrees ), without significant difference between right and left rotations. Associated motion components were small. During rotation in flexed head position, global range (134 degrees, SD: 24 degrees ) was comparable to the one in neutral flexion. But heterolateral bending, averaging 60% of the primary motion, was associated to flexed rotation. Significant reduction of all primary (but not conjunct) motions with age were obtained. Sex had no influence on cervical motion range. RELEVANCE: Our results agreed with previous observations, validating the methodology used. They thus constitute reference data of cervical out-of-plane motion for clinical applications.

Adolescent↗