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Bravo M J - - 1995
In calculating the precise speed of an object, the visual system must integrate motion measurements across time and space while keeping motion measurements from different objects separate. We examined whether an initial coarse estimate of local speed may be used to segregate the motions of different objects prior to a ...
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De Bruyn B - - 1995
For a continuous flow field depicting a combined translation and expansion, there exists a natural distribution of local motion directions whose mean direction corresponds to the direction of translation. A random sampling of this distribution may introduce spatial asymmetries and thus alter the mean direction. This statistical phenomenon has a ...
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Bles W - - 1995
A sensation of linear self-motion can be induced in a blindfolded stationary sitting subject, who keeps contact with a linearly moving platform (acceleration 0.1 m/s2) in the frontoparallel plane by means of a hand-over-hand walking action. When discordant suprathreshold vestibular information from the otoliths is added by moving the subject ...
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Zanker J M - - 1995
The subjective strength of a percept often depends on the stimulus intensity in a nonlinear way. Such coding is often reflected by the observation that the just-noticeable difference between two stimulus intensities (JND) is proportional to the absolute stimulus intensity. This behaviour, which is usually referred to as Weber's Law, ...
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Wenderoth P - - 1995
Experiment 1 demonstrates that, while the outline shapes of bilaterally symmetrical dot patterns play a role in symmetry detection, the removal of the outline by a surrounding random-dot annulus merely reduces performance by a fixed amount. It does not affect the relative salience of different symmetry-axis orientations. The converse is ...
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Watamaniuk S N - - 1995
Human observers can easily detect a signal dot moving, in apparent motion, on a trajectory embedded in a background of random-direction motion noise. A high detection rate is possible even though the spatial and temporal characteristics (step size and frame rate) of the signal are identical to the noise, making ...
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Evidence that luminant and equiluminant motion signals are integrated by directionally selective ...
Heidenreich S M - - 1995
Three experiments tested whether motion information for nonequiluminant (luminant) and equiluminant dots affects direction judgments when both types of stimuli are moving simultaneously in the same display. The motion directions for the two sets of dots were manipulated to produce four direction differences (0 degrees, 30 degrees, 60 degrees, and ...
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Orban G A - - 1995
The responses of macaque medial superior temporal (MST) cells to translation and to the optic-flow components-rotation, expansion/contraction, and deformation-were examined with particular regard to the speed tuning of MST cells for optic-flow stimuli and the effect of removing speed gradients from those stimuli. The use of position invariance as an ...
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Qian N - - 1995
It is well known that a stimulus composed of two independent sets of random dots moving in opposite directions produces a percept of two overlapping transparent surfaces moving across each other, while a counterphase grating composed of two identical sine wave gratings drifting in opposite directions does not. We recorded ...
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Edin B B - - 1995
The response of 70 cutaneous, low-threshold mechanoreceptors in the human median, radial and inferior alveolar nerves to well controlled brush stimuli moving across the receptive field was quantitatively studied. Microneurography was used to obtain the response of each to multiple velocities from 0.5 to 32 cm/sec in at least two ...
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Essick G K - - 1995
The mean firing rate evoked in 70 cutaneous, low-threshold mechanoreceptors in the human median, radial, and inferior alveolar nerves by stimulus motion across the skin was quantitatively studied. Moving stimuli, controlled for velocity, direction, and length of skin traversed, were provided by a servo-controlled motor that carried a brush across ...
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Rudolph K K - - 1994
Dynamic random-dot targets were used to study neural mechanisms underlying motion perception. Performance of cats with severely reduced numbers of cortical directionally selective neurons (reduced DS) was compared to that of normal animals. We assessed the spatial properties of the residual motion mechanism by measuring direction discriminations at various dot ...
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Qian N - - 1994
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 ...
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Malonek D - - 1994
We have used optical imaging based on intrinsic signals to explore the functional architecture of owl monkey area MT, a cortical region thought to be involved primarily in visual motion processing. As predicted by previous single-unit reports, we found cortical maps specific for the direction of moving visual stimuli. However, ...
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Edwards M - - 1994
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 ...
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Cornelissen F W - - 1994
It has been suggested that density modulated random-dot patterns can be used to study higher order pattern vision [Van Meeteren and Barlow (1981) Vision Research, 21, 765-777]. The high contrast dots of which the pattern is composed, are assumed to be reliably transduced and transmitted by the lower levels of ...
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Cropper S J - - 1994
Second-order Type I and Type II plaids were constructed by combining two random-dot gratings. Each component consisted of a dynamic random-dot field, the contrast of which was modulated by a drifting sinusoidal grating. Orienting the two components suitably and interleaving at 120 Hz allowed us to produce a two-dimensional plaid ...
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Smith A T - - 1994
Previous studies have shown that a random-dot kinematogram (RDK) comprising dots, each of which takes a random walk in direction or speed over time, can appear to flow in a single direction. This has been interpreted as evidence for the existence of a co-operative network linking neurons sensitive to different ...
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Norrsell U - - 1994
1. Tactile directional sensibility is considered to rely on the parallel processing of direction-contingent sensory data that depend on skin stretching caused by friction, and spatial cues that vary with time. A temperature-controlled airstream stimulus that prevented the activation of stretch receptors was used to investigate directional sensibility for the ...
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Schwinger J - - 1994
The electromagnetic field is assigned a self-consistent role in which abrupt slowing of the collapse produces radiation and the pressure of the radiation produces abrupt slowing. A simple expression is introduced for the photon spectrum. Conditions for light emission are proposed that imply a high degree of spatial localization. Some ...
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Sun M - - 1994
The two-dimensional organization of receptive fields (RFs) of 44 cells in the cat visual cortex and four cells from the cat LGN was measured by stimulation with either dots or bars of light. The light bars were presented in different positions and orientations centered on the RFs. The RFs found ...
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Hock H S - - 1994
A long row of evenly spaced dots is displaced on successive frames by half the distance between the dots. Although these stimuli are directionally ambiguous, spatially and temporally coherent unidirectional and oscillatory motion patterns are perceived as a result of the temporal persistence of competing in-phase and anti-phase directional biases, ...
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Murray R A - - 1994
Clinicians have used the same instrument (viz, Semmes-Weinstein pressure aesthesiometers [Research Design, Inc, Houston, TX] or "von Frey hairs") for tests of both contact detection and direction discrimination. However, patients' ability to discriminate direction may be underestimated by barely detectable moving stimuli. To determine whether the aesthesiometers underestimate direction discrimination, ...
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Saidpour A - - 1994
Interpolation across orientation discontinuities in simulated three-dimensional (3-D) surfaces was studied in three experiments with the use of structure-from-motion (SFM) displays. The displays depicted dots on two slanted planes with a region devoid of dots (a gap) between them. If extended through the gap at constant slope, the planes would ...
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I. King,L. Xu
This paper demonstrates how the Principal Component Analysis (PCA) learning can be used to extract the spatiotemporal characteristics of the receptive field from 1-D moving grating patterns. The results found in our experiment were similar to the linear inseparable spatiotemporal filters in agreement with neurophysiological findings. 1 Introduction The correct ...
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Wagner H - - 1994
1. Many neurons in the owl's midbrain are able to discriminate by their responses the motion of an acoustic source in one direction, the preferred direction, from the motion of the source in the opposite direction, the null direction. This differential response can be understood by the action of an ...
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Salzman C D - - 1994
Cognitive and behavioral responses to environmental stimuli depend on an evaluation of sensory signals within the cerebral cortex. The mechanism by which this occurs in a specific visual task was investigated with a combination of physiological and psychophysical techniques. Rhesus monkeys discriminated among eight possible directions of motion while directional ...
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Wattam-Bell J - - 1994
The sensitivity of 3-month-old infants to direction of motion in random-dot patterns was assessed by measuring coherence thresholds for the discrimination of a pattern, in which opposite directions were segregated into alternate horizontal strips, from an unsegregated pattern. The coherently moving dots had a displacement size of 0.16 deg (velocity ...
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McLean J - - 1994
A reverse correlation technique, which permits estimation of three-dimensional first-order properties of receptive fields (RFs), was applied to simple cells in areas 17 and 18 of cat. Two classes of simple cells were found. For one class, the spatial and temporal RF characteristics were separable, i.e. they could be synthesized ...
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McPherson L M - - 1994
In audition, sound energy is assigned to separate auditory "streams" following principles of organization that closely parallel the visual gestalt principles that guide the perception of distinct forms or objects. Metzger (1934) provided evidence for organization in vision based on similarity in the velocity of moving forms. If two dots ...
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Niemann T - - 1994
A transparent motion condition occurs when two different motion vectors appear at the same region of an image. Such transparency during self-motion has shown demonstrable effects on perception and on the underlying neurophysiology in the cortical and subcortical structures of primates. Presumably such stimulus conditions also influence oculomotor behavior. We ...
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Kappers A M - - 1994
Psychophysical thresholds for the detection of vorticity in the presence of a translational component are determined for human observers. Stimuli consist of sparse random-dot flow patterns. The detection of vorticity depends critically on the translational component. The curvature of the flow lines, however, cannot be the only factor limiting human ...
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Crook J M - - 1994
Directional tuning for motion of a long bar and a spot was compared quantitatively over a wide range of velocities in 23 simple cells of cat striate cortex whose "on" and "off" receptive field subregions had been mapped with optimally oriented, stationary flash-presented bars. Tuning curves were derived using stimuli ...
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Regan D - - 1994
The direction of motion in depth of a monocularly-viewed rigid sphere can be quantified in terms of the distance by which the sphere's centre will miss the centre of the pupil of the observing eye. If we express this distance as ns (where s is the sphere's radius and n ...
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Monen J - - 1994
Experiments were designed to establish whether we can use the optic flow to detect changes in our own velocity. Subjects were presented with simulations of forward motion across a flat surface. They were asked to respond as quickly as possible to a step increase in simulated ego-velocity. The smallest change ...
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Olausson H - - 1994
Spatial summation is known to influence the magnitude of sensation for stationary cutaneous stimuli. Yet analysis of moving stimuli may also be pertinent, since most stimuli that attract our attention involve movements over the skin surface. The present investigation dealt with the importance of spatial summation for the appreciation of ...
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Dzhafarov E N - - 1993
Observers reacted to the change in the movement of a random-dot field whose initial velocity, V0, was constant for a random period and then switched abruptly to another value, V1. The two movements, both horizontally oriented, were either in the same direction (speed increments or decrements), or in the opposite ...
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Prete F R - - 1993
Adult female praying mantises, Sphodromantis lineola (Burr.), were presented with computer-generated black rectangular stimuli that moved horizontally or vertically at 82 deg/s against a homogeneous white background. Both stimulus configuration (orientation in relation to direction) and the retinal location of the stimulus image affected the rate at which mantises responded ...
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Mizumori S J - - 1993
The hippocampal formation has been extensively studied for its special role in visual spatial learning and navigation. To ascertain the nature of the associations made, or computations performed, by hippocampus, it is important to delineate the functional contributions of its afferents. Therefore, single units were recorded in the lateral dorsal ...
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Tatemichi H - - 1993
We describe a feasibility study of a multiplexed holographic recording method onto a moving storage medium by using moving interference fringes caused by diffracted light beams that are generated from an acousto-optic deflector (AOD). The AOD, driven by amplitude-modulated electric signals, generates several diffracted beams with different frequencies because of ...
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Bauer R - - 1993
A comparison was made of the directional preferences of cat area 17 cells tested with two different stimuli, gratings and random-dot patterns. Depending on the stimulus, different distributions of direction preferences (anisotropies) were found in the same cells of the central representation of upper layers. With gratings most common preferred ...
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Prete F R - - 1993
Tethered adult female praying mantises, Sphodromantis lineola (Burr.), were presented with various computer-generated visual stimuli that moved against patterned or homogeneous white backgrounds in predetermined patterns and at predetermined speeds. The degrees to which the stimulus configurations elicited appetitive behaviors (attempting to approach and/or striking) indicated the relative degrees to ...
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Grzywacz N M - - 1993
1. We have investigated the facilitation of extracellularly recorded responses of ON-OFF directionally selective (DS) ganglion cells of the rabbit retina to two-slit preferred-direction apparent motion produced by both prolonged light steps, which simulate movement of an edge past two apertures, and light flashes, which simulate movement of a spot ...
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Amthor F R - - 1993
1. We have investigated the inhibitory mechanisms modulating the extracellularly recorded responses of ON-OFF directionally selective (DS) ganglion cells of the rabbit retina. Our investigations used both moving spots and apparent motion. The latter was produced by both prolonged light steps, which simulate movement of an edge, and light flashes, ...
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Lorenceau J - - 1993
We studied direction discrimination for lines moving obliquely relative to their orientation. Manipulating contrast, length and duration of motion, we found systematic errors in direction discrimination at low contrast, long length and/or short durations. These errors can be accounted for by a competition between ambiguous velocity signals originating from contour ...
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Olausson H - - 1993
1. The ability to tell the direction of a motion across the skin deserve attention for being an easily observed function which provides a sensitive test for disturbances of the peripheral and central nervous systems. The mode of operation, on the other hand, of this tactile directional sensibility is still ...
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Jones D L - - 1993
A recent study suggested that the preparation of movement direction, but not amplitude, may be selectively impaired by Parkinson's disease (PD). The authors examined the reprogramming of direction only, amplitude only, and direction and amplitude together, and included a control condition in which neither parameter was reprogrammed. The findings suggested ...
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Harris L R - - 1993
We evaluated the subcortical pathways' contribution to human adults' horizontal OKN by using a method similar to that used previously with cats (Harris & Smith, 1990; Smith & Harris, 1991). Five normal adults viewed plaids composed of two drifting sinusoidal gratings arranged such that their individual directions of drift were ...
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Treue S - - 1993
We measured the points of subjective equality of velocity for dynamic unidirectionally moving random-dot patterns with different amounts of transiency. The transiency was changed by varying the time a dot would move before being randomly replotted within the stimulus. The perceived velocity of patterns moving at intermediate velocities (4 or ...
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Raymond J E - - 1993
Opponent, or ratio, models of movement direction perception propose that pairs of analysers, sensitive to opposite directions, are linked in an opponent fashion. Alternatively, distribution models posit independence of movement direction analysers. To investigate analyser independence, a direction-selective adaptation experiment was conducted in which motion coherence thresholds for random-dot apparent ...
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