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Bernal Ximena E - - 2007
In its simplest form, communication is an interaction between a signaler and a receiver in which the signal has some probabilistic influence on the behavior of the receiver. For communication to proceed, the signal must be detected and perceived by the receiver; that is, the receiver must be within the ...
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Mysore Santosh G - - 2008
Motion is a potent cue for breaking camouflage in the natural world. To understand the neural basis of this phenomenon, one must utilize moving shapes defined by coherent motion of random texture elements against a similar, but stationary texture. To investigate how well neurons in area V4 process this novel, ...
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Baron Jerome - - 2007
The avian retinothalamofugal pathway reaches the telencephalon in an area known as visual wulst. A close functional analogy between this area and the early visual cortex of mammals has been established in owls. The goal of the present study was to assess quantitatively the directional selectivity and motion integration capability ...
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Neri Peter - - 2007
The response of vertebrate motion-sensitive neurons to a directional stimulus is affected by the direction of the stimulus that immediately preceded it. These nonlinear effects are also observed for orientation tuning and are typically interpreted as fast-scale adaptive changes. We verified that similar effects are observed for spiking tangential cells ...
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Yilmaz Ozgur - - 2007
Motion is known to distort visual space, producing illusory mislocalizations for flashed objects. Previously, it has been shown that when a stationary bar is flashed in the proximity of a moving stimulus, the position of the flashed bar appears to be shifted in the direction of nearby motion. A model ...
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Stanley James - - 2007
Human movement performance is subject to interference if the performer simultaneously observes an incongruent action. It has been proposed that this phenomenon is due to motor contagion during simultaneous movement performance-observation, with coactivation of shared action performance and action observation circuitry in the premotor cortex. The present experiments compared the ...
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Demb Jonathan B - - 2007
Direction selectivity represents a fundamental computation found across multiple sensory systems. In the mammalian visual system, direction selectivity appears first in the retina, where excitatory and inhibitory interneurons release neurotransmitter most rapidly during movement in a preferred direction. Two parallel sets of interneuron signals are integrated by a direction-selective ganglion ...
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Silvanto Juha - - 2007
Transcranial magnetic stimulation (TMS) allows one to investigate the effects of temporary interference of neural processing in neurologically intact subjects. In a previous study [J. Silvanto et al. (2007) Eur. J. Neurosci., 25, 1874-1881] we found that online TMS perceptually facilitates the attributes encoded by the least active neural populations. ...
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Thiel Andreas - - 2007
We investigate the capability of turtle retinal ganglion cell (RGC) ensembles to simultaneously encode multiple aspects of visual motion: speed, direction, and acceleration of moving patterns. Bayesian stimulus reconstruction reveals that the instantaneous firing rates of RGCs contain information about all of these stimulus properties. Stimulus velocity is mainly encoded ...
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Caplovitz G P - - 2007
Unlike the motion of a continuous contour, the motion of a single dot is unambiguous and immune to the aperture problem. Here we exploit this fact to explore the conditions under which unambiguous local motion signals are used to drive global percepts of an ellipse undergoing rotation. In previous work, ...
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Greene Ernest - - 2007
Most extant theories of shape perception assume or assert that various contour attributes, and in particular, the orientation, curvature and linear extent of the contours provide essential object recognition cues. The present study examined this proposal using discrete dots that marked locations on the outer boundary of namable objects, providing ...
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Gehres Martin - - 2007
Large field motion detection in goldfish, measured in the optomotor response, is based on the L-cone type, and is therefore color-blind (Schaerer & Neumeyer, 1996). In experiments using a two-choice training procedure, we investigated now whether the same holds for the detection of a small moving object (size: 8 mm ...
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Mateeff Stefan - - 2007
We presented a random dot pattern that moved horizontally for 1.6s within a stationary invisible aperture. The dots were periodically visible for 50 ms (visible phase) with lengths of the real motion 0-1.34 deg; for the next 50 ms their luminance was zero (invisible phase). The pattern was seen to ...
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Webb Ben S - - 2007
Physiological studies suggest that decision networks read from the neural representation in the middle temporal area to determine the perceived direction of visual motion, whereas psychophysical studies tend to characterize motion perception in terms of the statistical properties of stimuli. To reconcile these different approaches, we examined whether estimating the ...
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Bennett Patrick J - - 2007
Random dot cinematograms were used to probe motion perception in human observers ranging from 23 to 81 years of age. Stimuli were either broadband directional Noise, which produces no experience of global motion flow, or a narrower band directional Signal, which tended to produce experiences of coherent, global direction flow. ...
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Linares Daniel - - 2007
When a flash is presented aligned with a moving stimulus, the former is perceived to lag behind the latter (the flash-lag effect). We study whether this mislocalization occurs when a positional judgment is not required, but a veridical spatial relationship between moving and flashed stimuli is needed to perceive a ...
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Bours Roger J E - - 2007
Detection of apparent motion in random dot patterns requires correlation across time and space. It has been difficult to study the temporal requirements for the correlation step because motion detection also depends on temporal filtering preceding correlation and on integration at the next levels. To specifically study tuning for temporal ...
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Champion Rebecca A - - 2007
It has been shown that the perceived direction of a plaid with components of unequal contrast is biased towards the direction of the higher-contrast component [Stone, L. S., Watson, A. B., & Mulligan, J. B. (1990). Effect of contrast on the perceived direction of a moving plaid. Vision Research 30, ...
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Rushton Simon K - - 2007
A pair of projectiles travelling on parallel trajectories produce differing patterns of retinal motion when they originate at different distances. For an observer to recognise that the two trajectories are parallel she must "factor out" the effect of distance on retinal motion. The observer faces a similar problem when physically ...
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Kaneoke Yoshiki - - 2006
We present evidence to support the possibility that motion information is divided into two scalars: direction and speed, to integrate local motions over a wide spatial range. With various motion stimuli composed of numerous red and green dots, observers perceived that peripheral dots moved similar to central dots on the ...
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Hirahara Makoto - - 2006
When a stimulus of equally spaced parallel lines is displaced slightly in a direction perpendicular to the lines, low-speed motion toward the displacement direction can be perceived. Such a stimulus embodies both a low-speed and a high-speed component in opposite directions. The dominance of the former would result in the ...
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Tsui Sum Yin - - 2007
Motion signals contained within a stationary object projected on the fronto-parallel plane shift the object's apparent spatial position in the direction of the motion [see De Valois, R. L., & De Valois, K. K. (1991). Vernier acuity with stationary moving Gabors. Vision Research, 31(9), 1619-1626]. We report an analogous apparent ...
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Li Zu-Bin - - 2006
The transmission from a single subwavelength slit in a metal film with periodic dielectric bars on its surfaces has been analyzed numerically by the finite-difference time-domain method. Results show that the role of the periodic dielectric bars is just the same as that of the periodic grooves directly on the ...
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Sun Wenzhi - - 2006
Two types of ganglion cells (RGCs) compute motion direction in the retina: the ON-OFF direction-selective ganglion cells (DSGCs) and the ON DSGCs. The ON DSGCs are much less studied mostly due to the low encounter rate. In this study, we investigated the physiology, dendritic morphology and synaptic inputs of the ...
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Heuer Herbert - - 2006
Intermanual interactions are modulated by task requirements in the course of motor preparation. In particular, amplitude coupling is strong when identical amplitudes are specified concurrently for the 2 hands but relaxed when different amplitudes are specified. Similarly, directional coupling is symmetric when symmetric directions are specified concurrently but turns to ...
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Kamitani Yukiyasu - - 2006
Functional neuroimaging has successfully identified brain areas that show greater responses to visual motion and adapted responses to repeated motion directions. However, such methods have been thought to lack the sensitivity and spatial resolution to isolate direction-selective responses to individual motion stimuli. Here, we used functional magnetic resonance imaging (fMRI) ...
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Del Viva Maria Michela - - 2006
Successive presentations of Glass patterns (randomly positioned pairs of dots oriented in a coherent pattern) create a strong sense of global motion along the orientation of the pattern, but ambiguous in direction. Here we report that dynamic "anti-Glass" patterns, created by successive pairs of globally structured pairs of opposite polarity, ...
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Douglas R M - - 2006
The coherence thresholds to discriminate the direction of motion in random-dot kinematograms were measured in rats and mice. Performance was best in the rats when dot displacement from frame-to-frame was about 2 degrees, and frame duration was less than 100 ms. Mice had coherence thresholds similar to those of rats ...
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Edwards Mark - - 2006
The effect of signal intensity (proportion of dots moving in the same direction compared to noise dots that move in random directions) on perceived speed was investigated. It was found that increasing signal level decreased the perceived speed of the stimulus. This finding indicates that global-motion pooling processes play a ...
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Jaschinski Wolfgang - - 2006
The visual direction of a continuously presented monocular object is captured by the visual direction of a closely adjacent binocular object, which questions the reliability of nonius lines for measuring vergence. This was shown by Erkelens, C. J., and van Ee, R. (1997a,b) [Capture of the visual direction: An unexpected ...
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Dagnelie Gislin - - 2006
PURPOSE: To investigate the feasibility of adequate reading by recipients of future prosthetic visual implants through simulation in sighted observers. METHODS: Four normally sighted subjects used a video headset to view short-story segments at a sixth grade reading level, presented in 6- to 11-word paragraphs through a pixelizing grid defined ...
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Vajda Ildikó - - 2006
Temporal interactions in direction-sensitive complex cells in area 18 and the posteromedial lateral suprasylvian cortex (PMLS) were studied using a reverse correlation method. Reverse correlograms to combinations of two temporally separated motion directions were examined and compared in the two areas. A comparison to the first-order reverse correlograms allowed us ...
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Tang Hui - - 2006
An oral tactile interface was designed and evaluated to provide directional cues through the tactile channel, which may be utilized by a blind traveler to obtain directional guidance in outdoor navigation. The device was implemented as a mouthpiece with a microfabricated electrotactile display on top for tactile presentation onto the ...
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Snijders Hendrikus J - - 2007
Recent models of multisensory integration predict differential weighting of information from different sensory modalities in different spatial directions. This direction-dependent weighting account suggests a heavier weighting for vision in the azimuthal (left-right) direction and a heavier weighting for proprioception in the radial (near-far) direction. Visually induced reaching errors, as demonstrated ...
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Bocheva Nadejda - - 2006
The effects of surface markings on perceived motion direction were examined for a rotating sphere in a structure-from-motion display. The markings were dot patterns representing separate line segments or intersecting line segments (crosses) covering the surface of the sphere. The orientation of the surface markings and their intersection angles affected ...
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Curran William - - 2006
Neural adaptation and inhibition are pervasive characteristics of the primate brain and are probably understood better within the context of visual processing than with any other sensory modality. These processes are thought to underlie illusions in which one motion affects the perceived direction of another, such as the direction aftereffect ...
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Del Viva M Michela - - 2006
Here we report a new motion illusion where the prevailing motion direction is strongly influenced by the relative phase of the harmonic components of the stimulus. The basic stimulus is the sum of three sinusoidal contrast-reversing gratings: the first, the third, and the fifth harmonic of two square wave gratings ...
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Khang Byung-Geun - - 2006
We investigated the perception of illumination direction in images of 3-D convex objects under variations of light field and surface material properties. In a first experiment, we used an illumination-matching procedure in order to measure observers' ability to estimate the direction of illumination in images of 3-D polyhedra rendered under ...
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Puccini Gabriel D - - 2006
Neurons throughout the rat vibrissa somatosensory pathway are sensitive to the angular direction of whisker movement. Could this sensitivity help rats discriminate stimuli? Here we use a simple computational model of cortical neurons to analyze the robustness of directional selectivity. In the model, directional preference emerges from tuning of synaptic ...
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Gomi Tsutomu - - 2005
The purpose of this study was to compare direct and indirect detectors in terms of their presampled modulation transfer function (MTF), Wiener spectrum (WS), and noise-equivalent quanta (NEQ). Measurements were made on two flat-panel detectors, the GE Revolution XR/d (indirect) and Shimadzu Safire (direct) radiographic techniques. The presampled MTFs of ...
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Neri Peter - - 2006
Neurons in the fly lobula plate integrate motion signals over large regions of visual space in a directionally selective manner. This study is concerned with the details of this integration process. We used a stimulus consisting of a 4 x 4 lattice of locally moving Gabor patches, in which each ...
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Souman Jan L - - 2006
We investigated the relationship between compensation for the effects of smooth pursuit eye movements in localization and motion perception. Participants had to indicate the perceived motion direction, the starting point and the end point of a vertically moving stimulus dot presented during horizontal smooth pursuit. The presentation duration of the ...
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Neri Peter - - 2005
Flies, like humans, experience a well-known consequence of adaptation to visual motion, the waterfall illusion. Direction-selective neurons in the fly lobula plate permit a detailed analysis of the mechanisms responsible for motion adaptation and their function. Most of these neurons are spatially non-opponent, they sum responses to motion in the ...
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Watamaniuk Scott N J - - 2005
When the central region of an obliquely oriented line is bisected by a wide, vertical opaque occluder, observers misperceive the two line segments as being misaligned (the Poggendorff illusion). If the oblique line segment is replaced with a spot moving on an oblique trajectory, little if any misalignment is perceived. ...
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Dakin Steven C - - 2005
We used an equivalent noise (EN) paradigm to examine how the human visual system pools local estimates of direction across space in order to encode global direction. Observers estimated the mean direction (clockwise or counter-clockwise of vertical) of a field of moving band-pass elements whose directions were drawn from a ...
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Wilson J Anthony - - 2005
Using Glass patterns composed of isoluminant dots we have investigated the segregation and integration of chromatic information by the visual system. By measuring pattern detection when the chromaticities of the two elements forming a dot pair are varied (intradipole variation), we characterize integration at an early level of spatial processing. ...
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Kanazawa So - - 2006
We conducted four experiments on the development of motion perception in a total of 109 3- to 5-month-old infants using motion stimuli consisting of opposite-moving dots. A psychophysical study showed that adult subjects perceived two global planes with opposite-moving dots, but this global perception collapsed when paired opposite-moving dots were ...
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Gescheider George A - - 2005
An ALSCAL multidimensional scaling analysis in Euclidean space revealed that three orthogonal perceptual dimensions can account for the judged tactile dissimilarities of raised-dot patterns. Through magnitude estimates of various perceptual attributes, it was determined that the three dimensions consist of blur, roughness, and clarity. The only effect that selective adaptation ...
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Hilton Denis J - - 2005
Conditional directives are used by speakers to instruct hearers which actions are to be taken should certain events occur. The authors demonstrate that conditional directives are distinct from indicative conditionals in which speakers predict what is likely to be observed should certain events occur. The 1st set of experiments shows ...
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Khuu Sieu K - - 2006
The extent to which local speeds at different depths are averaged to determine global speed was determined using a version of the Global Dot Motion (GDM) stimulus. Judgments of the apparent speed of fast moving dots (4.05-10.53 deg/s) in the presence of slow moving dots (4.05 deg/s) were measured using ...
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