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PubMed2004

Motion-contrast computation without directionally selective motion sensors.

The detection of relative motion, i.e., motion contrast, has been reported for motion-sensitive neurons in several vertebrate systems, yet the mechanism underlying motion-contrast sensitivity remains unknown. An algorithm for computing motion contrast directly from the moving intensity distribution is proposed. In this algorithm, the time-dependent intensity distribution of the visual space is convolved with a periodic function. For coherent motion, the resulting convolution integral reduces to a traveling wave of fixed amplitude, while incoherent motion causes the amplitude to oscillate. The frequency of the amplitude oscillation provides a measure of motion contrast. The algorithm is successful in reproducing tuning curves derived from measurements of motion-contrast sensitivity in avian tectum and primate middle temporal area.

Algorithms↗
PubMed2002

The validity of using a video-based motion analysis system for measuring maximal area of fingertip motion and angular variation.

The aim of the study was to verify the application of a three-dimensional video motion analysis system to evaluate maximal fingertip motion area and angular variation of the hand by comparison and correlation with videofluoroscopic analysis. Eight normal subjects were recruited in this study. The maximal motion area of the fingertip and the angles of the metacarpal phalangeal (MP), proximal interphalangeal (PIP) and distal interphalangeal (DIP) joints in performing five sequential postures for functional evaluation of the hand were measured using a video motion analysis system and a fluoroscopy system respectively. The results indicated that the intraclass correlation coefficient (ICC) of the calculated maximal fingertip motion area between the two methods was 0.9597. The ICC for total active motion (TAM) measurements of three finger joints was 0.940 between the surface and bony landmarks by fluoroscopy, 0.952 between the surface landmarks from fluoroscopy and motion analysis, and 0.927 between the bony landmark from fluoroscopy and surface markers from motion analysis. The ICC for angular measurements between three different paired assessments was 0.9650, 0.8896 and 0.8799 for the MP, PIP and DIP joints respectively. The results indicate that motion analysis is a practical method for assessing impairment of the hand.

Adult↗
PubMed1994

Motion aftereffects of wagon wheels: motion aftereffects follow apparent rather than real movement.

Power and Moulden have proposed a model which accounts for the movement of gratings in apertures including the barber pole illusion. It predicts the direction of motion aftereffects which follow from perceived veridical motion and the direction of these aftereffects which follow from the illusory movement experienced during the barber pole illusion. At a perceptual level, the model predicts motion aftereffects will follow direction of apparent movement rather than veridical direction. Four experiments tested this prediction. In Exp. 1 a spiral was viewed under flickering light so it appeared to be moving in the direction opposite to true motion, and the aftereffect was opposite to the apparent direction. In Exp. 2 the spiral was viewed through a narrow aperture so that it was effectively a grating appearing to move in the opposite direction to veridical motion. Again, the motion aftereffect was opposite to the apparent rather than true direction of rotation. In Exp. 3 a sectored disc was used, and similar results were obtained. In Exp. 4 the sectored disc was videotaped so that it appeared to be rotating in the direction opposite to true motion. The after motion to this "wagon wheel" effect was opposite to its apparent direction of rotation on the screen. In all experiments the predictions were confirmed, thereby confirming the general principle that motion aftereffects follow apparent rather than real direction of movement.

Adolescent↗
PubMed2002

Are mechanisms for perception of biological motion different from mechanisms for perception of nonbiological motion?

We compared the integration of information over space and time for perceiving different configurations of moving dots: a walking person (biological motion), rigid three-dimensional shapes, and unidirectional coherent motion of all dots (translation). No performance differences in judging walking direction and coherent translation direction were obtained in conditions with constant presentation times and varying number of target dots (integration over space). Depending on the speed of the two-dimensional configurations judgments were either worse or better than the judgments of walking direction. The results for conditions with different presentation times (integration over time) show that information about biological motion is integrated over time that increases with increasing gait period, while two-dimensional unidirectional motion is integrated over constant time independent of speed. The effect is not due to the oscillatory nature of the biological motion since information about a rigid three-dimensional shape is summed over a constant time independent of the period of the motion cycle. This could be interpreted as different neural mechanisms mediating the temporal summation for walking direction compared to detecting the orientation of rigid structure, or the direction of two-dimensional unidirectional motion. Since biological motion is characterized by nonrigidity, it is possible that the form itself is integrated over time and not the motion pattern.

Algorithms↗
PubMed1998

A model for encoding multiple object motions and self-motion in area MST of primate visual cortex.

Many cells in the dorsal part of the medial superior temporal (MST) region of visual cortex respond selectively to specific combinations of expansion/contraction, translation, and rotation motions. Previous investigators have suggested that these cells may respond selectively to the flow fields generated by self-motion of an observer. These patterns can also be generated by the relative motion between an observer and a particular object. We explored a neurally constrained model based on the hypothesis that neurons in MST partially segment the motion fields generated by several independently moving objects. Inputs to the model were generated from sequences of ray-traced images that simulated realistic motion situations, combining observer motion, eye movements, and independent object motions. The input representation was based on the response properties of neurons in the middle temporal area (MT), which provides the primary input to area MST. After applying an unsupervised optimization technique, the units became tuned to patterns signaling coherent motion, matching many of the known properties of MST cells. The results of this model are consistent with recent studies indicating that MST cells primarily encode information concerning the relative three-dimensional motion between objects and the observer.

Animals↗
PubMed1997

Cancellation of motion artifact in MRI due to 2D rigid translational motion.

A new algorithm for cancelling MRI artifact due to translational motion in the image plane is described. Unlike the conventional iterative phase retrieval algorithm, in which there is no guarantee for the convergence, a direct method for estimating the motion is proposed. In the previous approach, the motions in the readout(x-) direction and the phase encoding(y-) direction are estimated simultaneously. However, the feature of the each x- and y-directional motion is different. Based on the analysis of their features, each x- and y-directional motion is cancelled by different algorithms in two steps. First, we notice that the x-directional motion corresponds to a shift of the x-directional spectrum of the MRI signal, so the x-directional motion can be cancelled by shifting the spectrum in inverse direction. Next, the y-directional motion is cancelled using a new constraint, with which the motion component and the true image component can be separated. The algorithm is shown to be effective by simulations.

Algorithms↗
PubMed2000

The effects of the lower extremity joint motions on the total body motion in sit-to-stand movement.

OBJECTIVE: The purpose of this study is to investigate the effects of lower extremity joint angular motions on the whole body linear motions in a sit-to-stand movement using a biomechanical model that describes the whole body linear velocity vector as functions of lower extremity joint angular velocities. DESIGN: Two-dimensional video analysis of whole body and joint kinematics. BACKGROUND: A biomechanical model that describes the whole body linear motions as functions of lower extremity joint angular motions is needed to provide clinically relevant information in clinical services and scientific research. METHODS: The linear velocity vector of the whole body motion during the sit-to-stand movement was partitioned into horizontal and vertical components and expressed as functions of lower extremity joint angular velocities for 10 healthy subjects. The coefficient of joint contribution to the whole body linear velocity vector was determined for each joint in each direction. RESULTS: The ankle and hip angular motions are critical to the development of the forward horizontal velocity of the whole body during the sit-to-stand movement. The knee and hip angular motions are critical to the development of the upward vertical velocity of the whole body during the sit-to-stand movement. CONCLUSIONS: The hip, knee, and ankle joint angular motions have various roles in whole body motions in different directions of the sit-to-stand movement. RELEVANCE: The model and the results of this study can be applied to study the control strategies, falls, and assessments of functional impairments in the sit-to-stand movement.

Adult↗
PubMed2006

Motion matters: secretory granule motion adjacent to the plasma membrane and exocytosis.

Total internal reflection fluorescence microscopy was used to monitor changes in individual granule motions related to the secretory response in chromaffin cells. Because the motions of granules are very small (tens of nanometers), instrumental noise in the quantitation of granule motion was taken into account. ATP and Ca2+, both of which prime secretion before fusion, also affect granule motion. Removal of ATP in permeabilized cells causes average granule motion to decrease. Nicotinic stimulation causes a calcium-dependent increase in average granule motion. This effect is more pronounced for granules that undergo exocytosis than for those that do not. Fusion is not preceded by a reduction in mobility. Granules sometimes move 100 nm or more up to and within a tenth of a second before fusion. Thus, the jittering motion of granules adjacent to the plasma membrane is regulated by factors that regulate secretion and may play a role in secretion. Motion continues until shortly before fusion, suggesting that interaction of granule and plasma membrane proteins is transient. Disruption of actin dynamics did not significantly alter granule motion.

Actins↗
PubMed2000

Simplified motion and loading compared to physiological motion and loading in a hip joint simulator.

Two wear tests were conducted using the Durham Hip Joint Wear Simulator to investigate the effects of simplified motion and loading on ultra-high molecular weight polyethylene (UHMWPE) acetabular cup wear rates. Bovine serum was used as a lubricant and a gravimetric technique was used to measure wear. The first wear test duration was 7.1 x 10(6) cycles and investigated the effect of simplified loading. This was achieved by using full physiological motion and loading for the first 5 x 10(6) cycles of the test, then physiological motion with simplified loading for the final 2.1 x 10(6) cycles of the wear test. The UHMWPE acetabular cup wear rates using full physiological motion and loading were 32.2 and 51.7 mm3/10(6) cycles against zirconia and CoCrMo femoral heads respectively. Using simplified loading the cup wear rates were 30.1 and 49.2 mm3/10(6) cycles against zirconia and CoCrMo respectively which was not significantly different from wear rates with physiological loading. The effect of simplified motion was investigated in a second wear test of 5.0 x 10(6) cycles duration. Physiological loading was applied across the prosthesis with physiological motion in the flexion/extension plane only. Mean wear of the acetabular component dropped to 0.197 mm3/10(6) cycles. The surfaces of all the acetabular cups were subject to gross examination, optical microscopy and scanning electron microscopy. No notable difference was observed between the cups subjected to physiological motion and loading and those subjected to simplified loading. The cups worn with a single plane of motion had a much smaller worn area and a notable difference in surface features to the other cups. Simplifed loading is therefore an acceptable simplification in simulator testing but simplifying motion to the flexion/extension plane axis only is unacceptable.

Acetabulum↗
PubMed2000

Binocular three-dimensional motion detection: contributions of lateral motion and stereomotion.

When an object moves along a trajectory in three-dimensional (3-D) space, there are potentially two orthogonal components that could be used to detect its motion: stereomotion resulting from the difference or disparity between the images in the right and left eyes, and lateral motion from the sum or average of the image motions in the right and left eyes. Using a suprathreshold search task for a target moving amid 3-D distractors, we found a range of 3-D trajectories for which increasing the stereomotion component did not improve detection. However, with larger stereomotion components, performance improved. The addition of random-motion noise to only the lateral motion component adversely affected the detection of both lateral motion and stereomotion. These data suggest that the visual system uses the average of the monocular image motions for the detection of a range of 3-D trajectories. In addition, a mechanism sensitive to the changing disparity may also be used but only for a very restricted range of 3-D motions.

Adult↗
PubMed1994

Transparent motion perception as detection of unbalanced motion signals. II. Physiology.

We investigated how the primate visual system solves the difficult problem of representing multiple motion vectors in the same part of the visual space--the problem of motion transparency. In the preceding companion article we reported that displays with locally well-balanced motion signals in opposite directions are perceptually nontransparent (i.e., one does not see two coherent moving surfaces) and that transparent displays always contain locally unbalanced motion signals. This is exemplified by our paired and unpaired dot patterns. Although both types of stimuli contain two sets of dots moving in opposite directions, the former is locally well balanced and appears like flicker while the latter gives a perception of two transparent surfaces. In this article we report our physiological recordings from areas V1 and MT of behaving monkeys, comparing single-cell responses to the paired and the unpaired dot patterns. Although a small proportion of directionally selective V1 cells responded differently to the two types of patterns, the average V1 responses could not reliably distinguish between the paired and the unpaired stimuli. A large fraction of MT cells, on the other hand, responded significantly better to the unpaired dot patterns than to the paired ones. Furthermore, the average response of all MT cells to the unpaired dot patterns was significantly higher than that to the paired dot patterns. These results demonstrate a neural correlate of the perceptual transparency at the level of MT. On the other hand, V1 cells do not generally discriminate between the transparent and nontransparent stimuli, indicating that V1 activity is not well correlated with the perception of motion transparency. Our results are consistent with a two-stage model for motion processing: the first stage measures local motion and the second stage introduces suppression if different directions of motion are present at a local region of the visual field. The first stage is located primarily in V1 and the second stage primarily in MT. Finally, we found a strong and negative correlation between the degree of the opponent-direction suppression of MT cells and their responses to flicker noise stimuli. This result suggests that one of the fundamental roles of the opponent-direction suppression in MT is noise reduction.

Animals↗
PubMed1983

Regional sequential motion in the normal left ventricle: nonuniform apical motion.

Timing of the onset and sequence of systolic regional wall motion was examined in the digitized left ventricular cineangiograms of 13 patients with angiographically normal coronary arteries and left ventricular function. Distance--time curves for anterior and inferior wall segments, the aortic valve plane, and apex point were compared to the volume--time curve in each ventricle. No significant differences were found in the onset of motion for the wall segments or for descent of the aortic valve where the sequence of motion was generally uniform. At the apex point, however, the onset of motion was significantly delayed. In addition, reduced velocity of motion in the first half of systole was followed by high velocity motion in the latter half. This apparent nonuniform apical motion may be explained by a geometric relationship of normally contracting myocardial wall fibers adjacent to a thin apical point which has relatively little or no contractile motion of its own.

Cineangiography↗
PubMed1983

Inhibition and facilitation of apparent motion by real motion.

Observers viewed a CRT display which contained both real and apparent motion. When the apparent motion was in the same direction as the real motion, the strength of the apparent motion was enhanced. Real motion in the opposite direction completely cancelled apparent motion. However, the appearance of the real motion was not affected by apparent motion.

Humans↗
PubMed1989

Monocular motion sensing, binocular motion perception.

The two-process account of motion perception and its binocular organization were addressed in experiments on apparent movement (AM) with three types of grating: sinusoidal; random bar width; and square-wave with missing fundamental (MF). Monocular MF gratings sampled four times per cycle of drift always appeared to move backwards. Here AM was unrelated to the spatial appearance of the pattern, and followed the motion of the dominant spatial frequency component (the third harmonic). We take this reversed AM to be characteristic of "short-range" motion sensors. It did not occur dichoptically, implying that the direction-selective mechanism of motion sensors is purely monocular. AM was seen with dichoptic presentation for all three types of grating. Performance improved with the length of the stimulus sequence, as predicted by probability summation. This result reconciles previous positive and negative findings on dichoptic AM. The perceived direction of dichoptic AM was consistent with polarity-selective matching of features over time (the "long-range process"). The most telling effect supporting feature-matching in dichoptic motion was that dichoptic MF motion reversed direction with a change in the visible features of the pattern (induced by changes in contrast and pulse duration); monocular apparent motion did not. Two routes from spatial frequency channels to the perception of object motion are discussed.

Contrast Sensitivity↗
PubMed1990

Perception of directional sampled motion in relation to displacement and spatial frequency: evidence for a unitary motion system.

Perception of directional motion was studied by displaying two images (F1 and F2) in rapid succession. The two images were identical except for a horizontal displacement of F2 with respect to F1. Observers reported the direction of horizontal motion over a wide range of displacements. The stimuli in Experiment 1 were one-dimensional gratings with spatial frequency between 0.125 and 6 c/deg. Motion was seen at all displacements to almost 0.5 cycles (counterphase) and remained invariant across spatial frequencies. In Experiment 2 the stimuli were band-pass filtered random-dot patterns. The bandwidth of the filters was 1 octave, and centre frequencies ranged from 0.75 to 12 c/deg. In every case, the response functions exhibited quasi-periodic oscillations related to structural properties of the images. One-dimensional analyses based on autocorrelation did not provide a satisfactory account of the data. By contrast, the data were fitted successfully by a two-dimensional analysis that integrated the responses of neighbouring motion detectors so as to yield a smooth motion flow field from which left-right directional motion could be derived. Practically and conceptually, the outcome supports a unitary motion system as distinct from separate systems subserving short-range and long-range motion.

Contrast Sensitivity↗
PubMed1991

Eye movements and the motion aftereffect: alternatives to the induced motion hypothesis.

It has been previously reported that prolonged unidirectional smooth pursuit often produces a negative motion aftereffect (MAE). This was believed to be caused by retinal image motion of stationary environmental contours during pursuit which subsequently produced a primary motion aftereffect in the tracking direction. The peripheral MAE then induced motion in the stationary tracking target resulting in illusory movement in the opposite direction. We have found that a negative MAE is also produced when the adapting field is devoid of any contours. Furthermore, the presence of a moving textured background in conjunction with smooth pursuit produced an MAE whose direction was inconsistent with the induced motion hypothesis. Since all examples of motion aftereffects in this study were associated with the pursuit aspect of the experiment rather than any interactions with background contours, it was proposed that the illusory motion had an oculomotor determinant. A scheme was tentatively outlined in which fixation suppression of an unregistered ocular drift following prolonged pursuit adaptation (pursuit after-nystagmus) produced the post-adaptive motion illusions.

Figural Aftereffect↗
PubMed1993

Functional segregation of color and motion perception examined in motion nulling.

We examine two hypotheses about the functional segregation of color and motion perception, using a motion nulling task. The most common interpretation of functional segregation, that motion perception depends only on one of the three dimensions of color, is rejected. We propose and test an alternative formulation of functional segregation: that motion perception depends on a univariate motion signal driven by all three color dimensions, and that the motion signal is determined by the product of the stimulus contrast and a term that depends only on the relative cone excitations. Two predictions of this model are confirmed. First, motion nulling is transitive: when two stimuli null a third they also null another. Second, motion nulling is homogeneous: if two stimuli null one another, they continue to null one another when their contrasts are scaled equally. We describe how to apply our formulation of functional segregation to other behavioral and physiological measurements.

Color Perception↗
PubMed1994

What direction of motion do we see if luminance but not colour contrast is reversed during displacement? Psychophysical evidence for a signed-colour input to motion detection.

To investigate the effects of colour upon motion detection, directional discrimination by human observers was determined using two-frame kinematograms in which the two classes of element composing the pattern could differ either in luminance alone (achromatic condition), or in both colour and luminance (chromatic condition). The elements in the second frame could either have the same colour/luminance as corresponding elements in the first frame, or they could be changed (swapped) in colour and/or luminance. The angular size of the elements was varied by changing the viewing distance. Changing colour between frames disrupted motion detection when the angular size of elements was large (0.9 deg) but not when they were small (0.225 deg), replicating a previous result. Detection of motion with chromatic patterns was generally superior to that with achromatic patterns, particularly with large element size. Luminance swap combined with colour swap produced the "reverse phi" phenomenon: however, when luminance was swapped with colour staying the same between frames, forward motion was seen, suggesting that forward motion based on colour dominated over reversed motion based on luminance. We conclude that signed chromatic information has an input to motion detection at low but less so at high spatial frequencies. Information across colour and luminance is combined in a final common pathway for motion detection, resulting either in enhancement if they are in agreement, or in disruption if they conflict.

Color Perception↗