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Results 251 - 300 of 654
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Bowns L - - 2001
Bowns (Vision Research, 36(22) (1996), 3685) argued that there are distinct features in two-component moving patterns (plaids) that if tracked move in the same direction as (1) the intersection of constraints direction (IOC) Adelson and Movshon (Nature, 300 (1992), 523); and (2) the vector sum direction (VS) Yo and Wilson ...
Lindsey D T - - 2001
Perceived directions of motion were measured for each of two superposed two-dimensional dynamic random patterns consisting of unfiltered or ring-filtered dense random-check (Julesz) textures. One pattern always moved in a cardinal direction (up, down, left, or right), and the other texture always moved in an oblique direction separated from the ...
Meerschaert M M - - 2001
The long-term limit motions of individual heavy-tailed (power-law) particle jumps that characterize anomalous diffusion may have different scaling rates in different directions. Operator stable motions [Y(t):t> or =0] are limits of d-dimensional random jumps that are scale-invariant according to c(H)Y(t)=Y(ct), where H is a dxd matrix. The eigenvalues of the ...
Moore T - - 2001
Previous studies have established that humans and monkeys with damage to striate cortex are able to detect and localize bright targets within the resultant scotoma. Electrophysiological evidence in monkeys suggests that residual vision also might include sensitivity to direction of visual motion. We tested whether macaque monkeys with longstanding lesions ...
Mast F W - - 2001
When viewing a wide-angle visual display, which rotates in the frontoparallel plane around the line of sight, observers experience an illusory shift of the direction of gravity; this shift leads to an apparent tilt of the body and displaces allocentric space coordinates. In this study, subjects adjusted an indicator to ...
Azzopardi P - - 2001
Some patients with brain damage affecting the striate cortex, though clinically blind in their field defects, can still discriminate visual stimuli when forced choice procedures are used. Such patients seem particularly sensitive to moving stimuli in their scotomata, though there are conflicting reports as to whether they can discriminate the ...
Bisley J W - - 2001
We applied electrical stimulation to physiologically identified sites in macaque middle temporal area (MT) to examine its role in short-term storage of recently encoded information about stimulus motion. We used a behavioral task in which monkeys compared the directions of two moving random-dot stimuli, sample and test, separated by a ...
Festa-Martino E - - 2001
When flickering dots are superimposed onto a drifting grating, the dots appear to move coherently with the grating. In this study we examine: (i) how the perceived direction of a compound stimulus composed of superimposed grating and dots, moving in opposite directions with equal speeds, is influenced by the relative ...
Verfaillie K - - 2000
During the perception of biological motion, the available stimulus information is confined to a small number of lights attached to the major joints of a moving actor. Despite this drastic impoverishment of the stimulus, the human visual apparatus organizes the swarm of moving dots in a vivid percept of a ...
Verghese P - - 2000
We measured the detectability of moving signal dots in dynamic noise to determine whether local motion signals are preferentially combined along an axis parallel to the direction of motion. Observers were asked to detect a signal composed of three dots moving in a linear trajectory among dynamic noise dots. The ...
Wiltschko W - - 2000
In a previous study, Australian silvereyes tested in autumn under monochromatic 565-nm green light at intensities of 2.1 and 7.5 mW m-2 preferred their normal northerly migratory direction, whereas they showed a significantly different tendency towards northwest at 15.0 mW m-2. Repeating these experiments in spring with silvereyes migrating southward, ...
Fenton A A - - 2000
Changing the angular separation between two visual stimuli attached to the wall of a recording cylinder causes the firing fields of place cells to move relative to each other, as though the representation of the floor undergoes a topological distortion. The displacement of the firing field center of each cell ...
Zugaro M B - - 2000
In order to navigate efficiently, animals can benefit from internal representations of their moment-to-moment orientation. Head-direction (HD) cells are neurons that discharge maximally when the head of a rat is oriented in a specific ("preferred") direction in the horizontal plane, independently from position or ongoing behavior. This directional selectivity depends ...
Hachisu I - - 2000
A theoretical light-curve model of the 1985 outburst of RS Ophiuchi based on a thermonuclear runaway model is presented. The system consists of a very massive white dwarf (WD) with an accretion disk and a red giant. The early phase of the V light curve is well reproduced only by ...
Levi R - - 2000
Cockroaches respond to the approach of a predator by turning away and then running. Three bilateral pairs of giant interneurons are involved in determining the direction of the sensory stimulus and setting the turn direction. Each of these six interneurons has a different directional response to wind stimuli. We have ...
Blais B - - 2000
Most simple and complex cells in the cat striate cortex are both orientation and direction selective. In this article we use single-cell learning rules to develop both orientation and direction selectivity in a natural scene environment. We show that a simple principal component analysis rule is inadequate for developing direction ...
Valdes-Sosa M - - 2000
Two interspersed and differently colored sets of dots were rotated in opposite directions and were perceived as superimposed transparent surfaces. Probes consisting of brief changes in dot motion direction were reported. Two probes affecting the same surface were discriminated accurately. The 2nd probe was discriminated poorly if it affected a ...
Schoumans N - - 2000
We examined the influence of context on exocentric pointing. In a virtual three-dimensional set-up, we asked our subjects to aim a pointer toward a target in two conditions. The target and the pointer were visible alone, or they were visible with planes through each of them. The planes consisted of ...
Treue S - - 2000
Dot patterns sliding transparently across one another are normally perceived as independently moving surfaces. Recordings from direction-selective neurons in area MT of the macaque suggested that this perceptual segregation did not depend on the presence of two peaks in the population activity. Rather, the visual system seemed to use overall ...
Merabet L - - 2000
The posteromedial lateral suprasylvian cortex represents a point of convergence between the geniculostriate and extrageniculostriate visual pathways. Given its purported role in motion analysis and the conflicting reports regarding the texture sensitivity of this area, we have investigated the response properties of cells in PMLS to moving texture patterns ("visual ...
Patterson R - - 2000
This study investigated the effect of exposure duration on the perceived direction of cyclopean Type I and Type II plaids moving in the X/Y plane. The cyclopean plaids were created from grating components defined by binocular disparity embedded in a dynamic random-dot stereogram. The results showed that the cyclopean Type ...
Dakin S C - - 2000
When two sets of intermixed dots move in different directions the perceived direction of each is considerably shifted [Marshak & Sekuler (1979). Science, 205, 1399-1401; Mather & Moulden, (1980). Quarterly Journal of Experimental Psychology, 32, 325-333)]. This phenomenon has been attributed to 'repulsive' interactions between channels tuned to different directions ...
Matthews N - - 2000
We investigated the extent to which motion repulsion and binocular motion rivalry depend on the distance between moving elements. The stimuli consisted of two sets of spatially intermingled, finite-life random dots that moved across each other. The distance between the dots moving in different directions was manipulated by spatially pairing ...
Ono H - - 2000
We examined Wheatstone's (1838 Philosophical Transactions of the Royal Society of London 128 371-394) claim that images falling on retinally corresponding points can be seen in two different directions, in violation of Hering's law of identical visual direction. Our analyses showed that random-dot stereograms contain stimulus elements that are conceptually ...
Genova B - - 2000
Experiments are presented in which a random dot pattern moved vertically upwards (velocity vector V(1)) and then abruptly changed its direction of motion by the angle alpha (velocity vector V(2)), either to the left or to the right, without changing the speed. Subjects performed simple reactions to the direction change, ...
Uttal W R - - 2000
We determined how much motion coherence was needed to detect a target group of four moving dots in a dynamic visual noise (DVN) background. The lifetimes of the trajectories of the target and that of the noise dots were the same. In addition to parallel trajectories and collinear dot arrangements, ...
Krekelberg B - - 2000
We extend the local energy model of position detection to cope with temporally varying position signals and the perception of relative position. The extension entails two main components. First, a form of persistence for the position signal based on the temporal impulse response function of the visual system. Secondly, we ...
Leung H C - - 2000
Responses from 69 Purkinje cells in the flocculus and paraflocculus of two rhesus monkeys were studied during smooth pursuit of targets moving along circular trajectories and compared with responses during sinusoidal pursuit and fixation. A variety of interesting responses was observed during circular pursuit. Although some neurons fired most strongly ...
Whitney D - - 2000
A flash that is presented aligned with a moving stimulus appears to lag behind the position of the moving stimulus. This flash-lag phenomenon reflects a processing advantage for moving stimuli (Metzger, W. (1932) Psychologische Forschung 16, 176-200; MacKay, D. M. (1958) Nature 181, 507-508; Nijhawan, R. (1994) Nature 370, 256-257; ...
Mateeff S - - 2000
A random dot pattern that moved within an invisible aperture was used to present two motions contiguously in time. The motions differed slightly either in speed (Experiments 1 and 3) or in direction (Experiments 2 and 4) and the subject had to discriminate the sign of the change (e.g. increment ...
Smith A T - - 2000
The mechanisms underlying the parsing of a spatial distribution of velocity vectors into two adjacent (spatially segregated) or overlapping (transparent) motion surfaces were examined using random dot kinematograms. Parsing might occur using either of two principles. Surfaces might be defined on the basis of similarity of motion vectors and then ...
Curran W - - 2000
Phenomenal transparency in random-dot kinematograms is abolished when two motion directions are 'locally-balanced' by pairing limited-lifetime dots at each location [Qian, Andersen and Adelson (1994). Journal of Neuroscience, 14, 7357-7366]. Qian et al. also report that locally-paired stimuli appear as directionless flicker when the paired dots differ in their directions ...
Kitajima N - - 1999
A moving light stimulus produced a sensation of motion for a stationary sound stimulus presented simultaneously, which was called the dynamic visual capture by Mateeff, Hohnsbein, and Noack in 1985. The present study examined whether the moving light stimulus might induce a perceptual shift in the velocity, that is, the ...
Sereno M E - - 1999
This study investigates how mechanisms for amplifying 2-D motion contrast influence the assignment of 3-D depth values. The authors found that the direction of movement of a random-dot conveyor belt strongly inclined observers to report that the front surface of a superimposed, transparent, rotating, random-dot sphere moved in a direction ...
Liu C H - - 1999
Face recognition in photographic positive and negative was examined in a same/different matching task in five lighting direction conditions using untextured 3-D laser-scanned faces. The lighting directions were +60, +30, 0, -30 and -60 degrees, where negative values represent bottom lighting and positive values represent top lighting. Recognition performance was ...
Ledgeway T - - 1999
The ability to integrate local second-order motion signals over space and time was examined using random-dot-kinematograms (RDKs) in which the dots were defined by spatial variation in the contrast, rather than luminance, of a random noise field. When either the speeds or the directions of the individual dots were selected ...
Cavaco S - - 1999
In this paper we present an acoustic motion detection system to be used in a small mobile robot. While the first purpose of the system has been to be a reliable computational implementation, cheap enough to be built in hardware, effort has also been taken to construct a biologically plausible ...
Chapman T - - 1999
Crickets are able to extract directional information about a wind stimulus through the filiform hairs located on their cerci. This paper describes the design and testing of a neuromorphic sensor that aims to achieve a close correlation with both the physical and functional properties of these hairs. An integrate and ...
Banton T - - 1999
Adults combine different local motions to form a global percept of motion. This study explores the origins of this process by testing how perturbations of local motion influence infants' sensitivity to global motion. Infants at 6-, 12-, and 18-weeks of age viewed random dots moving with a gaussian distribution of ...
van Assen M A - - 1999
Visual interpolation between dots responsible for rectilinear versus curvilinear contour interpretation was examined with the psychophysical forced directional response (FDR) paradigm. Regular four-dot polygon segments, together with a target dot, were presented to the subjects for 150 ms. Subjects were required to indicate the direction of deviation of the target ...
Masson G S - - 1999
Motion transparency requires that the visual system distinguish different motion vectors and selectively integrate similar motion vectors over space into the perception of multiple surfaces moving through or over each other. Using large-field (7 degrees x 7 degrees) displays containing two populations of random-dots moving in the same (horizontal) direction ...
Bremmer F - - 1999
Successful navigation through an environment requires precise monitoring of direction and distance traveled ("path integration" or "dead reckoning"). Previous studies in blindfolded human subjects showed that velocity information arising from vestibular and somatosensory signals can be used to reproduce passive linear displacements. In these studies, visual information was excluded as ...
Matthews N - - 1999
The motion of an object can be described by a single velocity vector, or equivalently, by direction and speed separately. Similarly, our ability to see subtle differences in the motion of two objects could be constrained by either a velocity-based sensory response, or separate sensory responses to direction and speed. ...
Alexander K R - - 1999
We used a motion coherence paradigm to test the hypothesis that patients with retinitis pigmentosa (RP) have difficulty discriminating the direction of spatial displacements because of a random loss of motion-sensitive units owing to cone photoreceptor dropout. Minimum (Dmin) and maximum (Dmax) displacement thresholds of patients with typical RP or ...
Clifford C W - - 1999
Random dot kinematograms were used to simulate radial, rotational and spiral optic flow. The stimuli were designed so that, while dot speed increased linearly with distance from the centre of the display, the density of dots remained uniform throughout their presentation. In two experiments, subjects were required to perform a ...
van der Zwan R - - 1999
PURPOSE: This experiment reports the independence of first- and second-order processing mechanisms in form perception. METHODS: Symmetrical dot patterns were created using either luminance-increment dots (luminance above background), or texture-defined dots (average luminance equal to background). The proportion of luminance increment or texture dots defining each pattern was varied among ...
Wright M J - - 1999
We address the question of how the visual system analyses changes in direction. Using plaid stimuli, we define type O direction changes which entail a change in the orientations of the plaid components, and type V direction changes in which the orientations of the components remain constant, relative to the ...
Edwards M - - 1999
A number of experiments were conducted to compare the ability of observers to extract unidirectional and bidirectional (transparent) global-motion signals. In the unidirectional condition, the noise signal consisted of purely randomly-moving dots while in the bidirectional condition, a number of the randomly moving dots were replaced by the same number ...
Lee S H - - 1999
In several experiments, it was found that global perception of spatial form can arise exclusively from unpredictable but synchronized changes among local features. Within an array of nonoverlapping apertures, contours move in one of two directions, with direction reversing randomly over time. When contours within a region of the array ...
Shea S J - - 1999
Patients with early disruptions of binocularity show cortical directional asymmetries in their steady state monocular VEP response to oscillatory motion. The VEP directional asymmetry is characterized by significant first harmonic components that show a 180 degrees difference in the response phase between the two eyes. By contrast, the normal response ...
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