Search Results
Results 301 - 350 of 654
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Sabatini S P - - 1999
Within a linear field approach, an architectural model for simple cell direction selectivity in the visual cortex is proposed. The origin of direction selectivity is related to recurrent intracortical interactions with a spatially asymmetric character along the axis of stimulus motion. No explicit asymmetric temporal mechanisms are introduced or adopted. ...
Murthy A - - 1999
Intracortical inhibition contributes to direction selectivity in primary visual cortex, but how it acts has been unclear. We investigated this problem in simple cells of cat area 17 by taking advantage of the link between spatiotemporal (S-T) receptive-field structure and direction selectivity. Most cells in layer 4 have S-T-oriented receptive ...
Mateeff S - - 1999
Recently Dzhafarov et al. presented a model explaining data on simple reaction time (RT) to unidimensional velocity changes. The authors suggested that having a motion with an initial velocity V0, the velocity change detection system is reinitialized by means of a "subtractive normalization" process. Therefore, any abrupt change from V0 ...
Hibbard P B - - 1999
Recent physiological studies have established that cortical cells that are tuned for the direction of motion may also exhibit tuning for binocular disparity. This tuning does not appear to provide any advantage in discriminating the direction of global motion in random-dot kinematograms. Here we investigated the possibility that this tuning ...
Zhang T - - 1999
Optokinetic nystagmus is a reflex to stabilize an object image on the retina by compensatory eye movements. In lower vertebrates, the nucleus of the basal optic root participates in generating this reflex. Visual responses of 135 neurons were extracellularly recorded from the nucleus in pigeons and their receptive field properties ...
Ishiguchi A - - 1999
In the present study, we dealt with the problem of whether a symmetrical structure can influence the discrimination of the depth separation of overlapped dot planes. We investigated this problem with the use of both direct and indirect methods. In the direct method, we presented three or two overlapped dot ...
Eisen M D - - 1999
The symmetry of chick cochlear hair bundle motion was examined in this study. Isolated segments from the basilar papilla were incubated in vitro in either normal or low calcium medium, which is known to disrupt tip links. Stereociliary bundles, stimulated with an oscillating water microjet, were oriented in profile and ...
Jamieson J - - 1999
Two principles are presented that describe directional confounds associated with baseline differences: Principle 1: Change scores are confounded with baseline whenever data are skewed. Principle 2: When baseline differences are real, ANCOVA has a directional bias that magnifies differences in one direction and masks those in the other direction. Both ...
Sekuler A B - - 1999
When identical visual targets move directly toward and then past one another, they appear either to stream past one another or to bounce off each other. Bertenthal et al (1993 Perception 22 193-207) accounted for the relative strengths of these two percepts by invoking a directional bias, arising from cooperative ...
Rudolph K - - 1999
We examined the nature and the selectivity of the motion deficits produced by lesions of extrastriate areas MT and MST. Lesions were made by injecting ibotenic acid into the representation of the left visual field in two macaque monkeys. The monkeys discriminated two stimuli that differed either in stimulus direction ...
Humphrey A L - - 1998
Strobe rearing reduces direction selectivity in area 17 by altering spatiotemporal receptive-field structure. J. Neurophysiol. 80: 2991-3004, 1998. Direction selectivity in simple cells of cat area 17 is linked to spatiotemporal (S-T) receptive-field structure. S-T inseparable receptive fields display gradients of response timing across the receptive field that confer a ...
Pirttiniemi P - - 1998
Normal asymmetry in the area of the craniofacial skeleton can be directional or fluctuating in nature. Directionality can in principle be found in three dimensions: anteroposterior, cranio-caudal, and asymmetries in the left-right dimension. When it comes to directional left right differences, an explanation has been difficult to find, although expressions ...
Grzywacz N M - - 1998
The two major excitatory synapses onto ON-OFF directionally selective (DS) ganglion cells of the rabbit retina appear to be nicotinic cholinergic and NMDA glutamatergic. Blockade of either of these synapses with antagonists does not eliminate directional selectivity. This suggests that these synapses may have complementary roles in the computation of ...
Grzywacz N M - - 1998
1. A model for retinal directional selectivity postulates that GABAergic inhibition of responses to motions in the null (anti-preferred) direction underlies this selectivity. An alternative model postulates that besides this inhibition, there exists an asymmetric, nicotinic acetylcholine (ACh) input from starburst amacrine cells. It is possible for the latter but ...
Edwards M - - 1998
The ability of observers to discriminate differences in global-motion-signal strength (that is the proportion of coherently moving dots in a field of randomly moving dots) was determined for both first and second-order stimuli. Observers could accurately discriminate differences in signal intensity for all reference signal levels tested; 20-100%. A similar ...
Raymond J E - - 1998
Although recent fMRI and single unit recording studies have shown that attention modulates neural activity in motion sensitive areas of extrastriate cortex, these approaches cannot reveal qualitative or quantitative effects of attention on perception of motion. To investigate this, we asked observers to select one of two orthogonal directions in ...
Hohnsbein J - - 1998
We studied the ability of human observers to detect abrupt changes in velocity of motion of a random dot pattern. The pattern moved horizontally for 0.9 s at velocity V0, then changed to V1 either in speed, or in direction for a time T and returned to the initial motion. ...
Britten K H - - 1998
It is not known whether psychophysical performance depends primarily on small numbers of neurons optimally tuned to specific visual stimuli, or on larger populations of neurons that vary widely in their properties. Tuning bandwidths of single cells can provide important insight into this issue, yet most bandwidth measurements have been ...
Rosenberg A F - - 1998
Visual-movement sensitivity of neurons in the turtle's accessory optic system was investigated. Neuronal responses to stimulus direction and speed were analyzed to determine whether they reflect processing by a one-dimensional encoder of visual motion or whether they indicate directional integration of presynaptic direction-sensitive responses whose maximal-response directions are distributed. Both ...
Gros B L - - 1998
We measured motion-detection and motion-discrimination performance for different directions of motion, using stochastic motion sequences. Random-dot cinematograms containing 200 dots in a circular aperture were used as stimuli in a two-interval forced-choice procedure. In the motion-detection experiment, observers judged which of two intervals contained weak coherent motion, the other internal ...
Rubin CM - - 1998
The Sierra Madre fault, along the southern flank of the San Gabriel Mountains in the Los Angeles region, has failed in magnitude 7.2 to 7.6 events at least twice in the past 15,000 years. Restoration of slip on the fault indicated a minimum of about 4.0 meters of slip from ...
Kautz D - - 1998
Many neurons in the barn owl's inferior colliculus (IC) exhibit auditory motion-direction sensitivity (MDS), i.e., they respond more to motion of a sound source in one direction than to motion in the opposite direction. We investigated the cellular mechanisms underlying the phenomenon of auditory MDS by microiontophoretically applying gamma-aminobutyric acid ...
Hinks R S - - 1998
Chemical shift artifacts and other off-resonance spatial shifts in 2DFT MRI arise from the linear time dependence in the k-space data in the readout direction. Introduction of a view-dependent time shift of the readout window adds a time dependence to the phase-encoding direction and results in a virtual frequency-encoding direction ...
Edwards M - - 1998
Several experiments were conducted to investigate the role of speed in global-motion processing; the extraction of the direction of motion of a small subset of coherently-moving (signal) dots in a stimulus in which the other (noise) dots move in random directions. The specific aim of the experiments was to determine ...
Paolini M - - 1998
Extracellular recordings obtained from the extrastriate cortex of the California ground squirrel, a diurnal sciurid, show that large receptive fields and a strong direction selectivity are present in the middle lateral area (ML) and the lateral area (L), located laterally to V2 and V3. Direction selectivity was tested by presenting ...
Braun D - - 1998
Unilateral lesions in the posterior parietal cortex can degrade motion perception in the contralesional visual hemifield. Our aim was to investigate whether deficits caused by cortical lesions may be different for first- and second-order motion perception, and to study the time scale of any potential recovery. In nine patients with ...
Worringham C J - - 1998
The basis of directional stimulus-response compatibility was studied using a task in which 128 participants moved a cursor into targets with a joystick, resembling the operation of certain industrial and construction equipment. Compatible and incompatible versions of three alternative compatibility principles were compared in all combinations. Visual Field (VF) compatibility ...
Oglesby DD - - 1998
Dynamic simulations of earthquakes on dipping faults show asymmetric near-source ground motion caused by the asymmetric geometry of such faults. The ground motion from a thrust or reverse fault is larger than that of a normal fault by a factor of 2 or more, given identical initial stress magnitudes. The ...
Lindsey D T - - 1998
Interactions in the perception of motion transparency were investigated using a signal-detection paradigm. The stimuli were the linear sum of two independent, moving, random-check "signal" textures and a third texture consisting of dynamic random "noise." Performance was measured as the ratio of squared signal and noise contrasts was varied (S2/N2). ...
Brown R J - - 1998
Motion processing in humans and monkeys exhibit a directional asymmetry during infancy which is not present in adults except following abnormal visual rearing conditions. To characterize the time course for maturation of a symmetric response, we measured the monocular visually evoked potential (MVEP) response to 0.26 c/deg gratings oscillating horizontally ...
Geesaman B J - - 1998
We recently reported a new motion illusion where dots in expanding random dot patterns appear to move faster than those in rotation patterns despite having the same physical speed distributions. In the current paper, we compared expansion and rotation motion to translational motion and found that the perceived dot speed ...
Mason C R - - 1998
This study examined the directional modulation of dorsal premotor (PMd) cells as a function of time in an instructed delay, reaching task that systematically varied direction and accuracy constraints. In two monkeys, the activity of 150 PMd cells was recorded and the preferred direction (PD) of the firing as a ...
Alexander K R - - 1998
We compared maximum displacement thresholds (Dmax) with minimum displacement thresholds (Dmin) in patients with retinitis pigmentosa (RP) in order to characterize the nature of their visual disability, as well as to assess possible models of foveal vision loss. Thresholds for discriminating the direction of the spatial displacement of random dot ...
Liu Z - - 1998
We take issue with theories about the direction specificity in perceptual learning of motion discrimination. Trials of motion discrimination in two opposite directions were interleaved in uneven proportions (2:1). Human subjects improved faster in the direction with less frequent trials, indicating that learning transferred from the more frequent to the ...
Glennerster A - - 1998
The upper displacement limit for motion was compared with the upper disparity limit for stereopsis using two-frame random dot kinematograms or briefly presented stereograms. dmax (the disparity/displacement at which subjects make 20% errors in a forced-choice paradigm) was found to be very similar for motion and stereo at all dot ...
Gegenfurtner K R - - 1998
Contrast thresholds for identification of the direction of motion were determined for sinusoidal gratings and plaid patterns moving in eight possible directions. Since plaid patterns are the sum of two component gratings, a prediction of the thresholds for plaids can be made by assuming that the motions of both component ...
Lewis J E - - 1998
The local bend is a directed behavior produced by the leech, Hirudo medicinalis, in response to a light touch. Contraction of longitudinal muscles near the touched location results in a bend directed away from the stimulus. We quantify the relationship between the location of touch around the body perimeter and ...
Jiang Y - - 1998
Five experiments were designed to determine whether a rotating, transparent 3-D cloud of dots (simulated sphere) could influence the perceived direction of rotation of a subsequent sphere. Experiment 1 established conditions under which the direction of rotation of a virtual sphere was perceived unambiguously. When a near-far luminance difference and ...
Watamaniuk S N - - 1998
Human observers can simultaneously encode direction information at two different scales, one local (an individual dot) and one global (the coherent motion of a field of dots distributed over a 10 degrees-diameter display). We assessed whether encoding global motion would preclude the encoding of a local trajectory component and vice ...
Rauber H J - - 1998
While humans are very reliable (i.e. give highly reproducible answers) when repeatedly judging the direction of a moving random-dot pattern (RDP) we find that their accuracy (i.e. the direction they so reliably report) shows systematic errors. To quantify these errors, we presented a complete set of closely spaced directions and ...
Lewald J - - 1998
This study investigates the influence of eye position on the localization of a free-field sound source by employing a pointing method. While fixating visual targets in various directions, the subjects indicated the perceived direction of a sound source by adjusting the azimuthal angle of a swivel pointer. The perceived sound ...
Giddon D B - - 1997
The purpose of this study was to assess whether the magnitude of the extreme horizontal or vertical deformations of morphed facial features influenced judgments of acceptability or preference of the facial soft tissue profile. Twelve judges responded to 5 changing features of 2 faces with clinically divergent malocclusions under 3 ...
Imig T J - - 1997
Monaural spectral contrast mechanism for neural sensitivity to sound direction in the medial geniculate body of the cat. J. Neurophysiol. 78: 2754-2771, 1997. Central auditory neurons vary in sound direction sensitivity. Insensitive cells discharge well to all sound source directions, whereas sensitive cells discharge well to certain directions and poorly ...
Festa E K - - 1997
The minimum information necessary to specify motion requires a change in position across time. Previous studies have shown that human motion measurements improve with more than two frames of motion. This study clarifies how motion information is integrated to produce the best speed and direction discrimination. Using random-dot kinematograms, fine-direction ...
Poirier P - - 1997
Responses of high-frequency primary auditory cortex (A1) neurons of the cat to noise stimulation were obtained in a quasianechoic chamber using a static and an apparently moving stimulus presented at similar azimuths. Simulated motion toward right or left as well as different simulated velocities were used. Under static stimulation, most ...
Barlow H - - 1997
In the random dot kinematograms used to analyze the detection of coherent motion in the middle temporal visual area (MT) and in psychophysical experiments the exact way that dots are paired between successive presentations is not known by the observer. We show how to calculate the limit to coherence threshold ...
Watanabe T - - 1997
Physically unidirectional motion of short-lived random dot arrays was found to perceptually decompose into two motion components (velocity decomposition) in a configuration in which two squares appear to partially overlap transparently (surface decomposition). In the experiments in which the velocity of the short-lived random dots in the overlapping area was ...
Ito H - - 1997
An interaction in apparent motion between perceived three-dimensional forms defined by stereopsis and local luminous elements is reported. Vertical stripes of cyclopean square gratings were simulated by random-dot stereograms. Alternation of two-frame stereograms whose phases differed by 90 deg caused two kinds of percepts, planes' motion in depth (first-order stereoscopic ...
Single S - - 1997
The extraction of motion information from time varying retinal images is a fundamental task of visual systems. Accordingly, neurons that selectively respond to visual motion are found in almost all species investigated so far. Despite its general importance, the cellular mechanisms underlying direction selectivity are not yet understood in most ...
Serpetopoulos C - - 1997
It is well-known that flying dots (muscae volitantes) in posterior vitreous detachment gradually disappear. An analogy for this phenomenon is the optical effect of planets casting conic shadows as they are lighted by the sun (in this case the pupil serves as the light source) and these shadows shrink as ...
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