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PubMed2003

Sound recognition and localization in man: specialized cortical networks and effects of acute circumscribed lesions.

Functional imaging studies have shown that information relevant to sound recognition and sound localization are processed in anatomically distinct cortical networks. We have investigated the functional organization of these specialized networks by evaluating acute effects of circumscribed hemispheric lesions. Thirty patients with a primary unilateral hemispheric lesion, 15 with right-hemispheric damage (RHD) and 15 with left-hemispheric damage (LHD), were evaluated for their capacity to recognise environmental sounds, to localize sounds in space and to perceive sound motion. One patient with RHD and 2 with LHD had a selective deficit in sound recognition; 3 with RHD a selective deficit in sound localization; 2 with LHD a selective deficit in sound motion perception; 4 with RHD and 3 with LHD a combined deficit of sound localization and motion perception; 2 with RHD and 1 with LHD a combined deficit of sound recognition and motion perception; and 1 with LHD a combined deficit of sound recognition, localization and motion perception. Five patients with RHD and 6 with LHD had normal performance in all three domains. Deficient performance in sound recognition, sound localization and/or sound motion perception was always associated with a lesion that involved the shared auditory structures and the specialized What and/or Where networks, while normal performance was associated with lesions within or outside these territories. Thus, damage to regions known to be involved in auditory processing in normal subjects is necessary, but not sufficient for a deficit to occur. Lesions of a specialized network was not always associated with the corresponding deficit. Conversely, specific deficits tended not be associated predominantly with lesions of the corresponding network; e.g. deficits in auditory spatial tasks were observed in patients whose lesions involved to a larger extent the shared auditory structures and the specialized What network than the specialized Where network, and deficits in sound recognition in patients whose lesions involved mostly the shared auditory structures and to a varying degree the specialized What network. The human auditory cortex consists of functionally defined auditory areas, whose intrinsic organization is currently not understood. In particular, areas involved in the What and Where pathways can be conceived as: (1) specialized regions, in which lesions cause dysfunction limited to the damaged part; observed deficits should be then related to the specialization of the damaged region and their magnitude to the extent of the damage; or (2) specialized networks, in which lesions cause dysfunction that may spread over the two specialized networks; observed deficits may then not be related to the damaged region and their magnitude not proportional to the extent of the damage. Our results support strongly the network hypothesis.

Acute Disease↗
PubMed1998

Perception of motion and qEEG activity in human adults.

This study was designed to relate visual perception of motion to cortical activity, by evaluation of the association of quantified electroencephalogram (qEEG) parameters with a video film projection. The EEG was recorded from 14 sites according to the International 10-20 system and a common average reference was used. Forty right-handed volunteers (mean age = 24 years) were examined. The video film consisted of 20 s sequences showing still shots and moving shots with human movements or object movements. The EEG was then subjected to spectral analysis; the spectral powers for the theta, alpha and beta bands were calculated for 14 s epochs and compared with sequences of the video film. All analyses were based on logarithmically transformed absolute spectral power values. The power values of each frequency band were analysed in a 3-way repeated measure ANOVA (Hemisphere x Electrode x Sequence). The results were represented by EEG cartography. Significant decreases in the alpha 1, beta 1 and beta 2 power values of EEG in centro-parietal regions of both hemispheres were shown during perception of human motion sequences. This suggests participation of the sensorimotor cortex during visual observation of human motion.

Adolescent↗
PubMed1999

Bistability in the perception of motion and stationarity: effects of temporal asymmetry.

Evidence for bistability in the perception of motion and stationarity was obtained for a displaced dot-figure embedded in a background of randomly moving noise dots. In the temporal symmetry condition, the figure was presented for the same duration in its two locations; either figure motion or random motion was perceived, depending on the number of noise dots. In the temporal asymmetry condition, the figure was presented for different durations in its two locations; figure motion, a single, stationary figure in a fixed position, or random noise was perceived, again depending on the number of noise dots. Competition between these percepts was established by an analysis of switching rates and by an experiment demonstrating the presence of hysteresis as noise levels were gradually increased and decreased across the figure-motion and figure-stationarity boundaries. This evidence for bistability in the perception of figure motion and figure stationarity (one or the other, but not both, was perceived for the same stimulus) suggested the presence of strong inhibitory competition between motion- and position-detecting mechanisms.

Adult↗
PubMed2006

A single system explains human speed perception.

Motion is fully described by a direction and a speed. The processing of direction information by the visual system has been extensively studied; much less is known, however, about the processing of speed. Although it is generally accepted that the direction of motion is processed by a single motion system, no such consensus exists for speed. Psychophysical data from humans suggest two separate systems processing luminance-based fast and slow speeds, whereas neurophysiological recordings in monkeys generally show continuous speed representation, hinting at a single system. Although the neurophysiological findings hint at a single system, they remain inconclusive as only a limited amount of cells can be measured per study and, possibly, the putative different motion systems are anatomically separate. In three psychophysical motion adaptation experiments, we show that predictions on the basis of the two-motion system hypothesis are not met. Instead, concurrent modeling showed that both here-presented and previous data are consistent with a single system subserving human speed perception. These findings have important implications for computational models of motion processing and the low-level organization of the process.

Adaptation, Physiological↗
PubMed1996

Cooperative interactions and the perception of motion and stationarity for directionally ambiguous apparent-motion stimuli.

Evidence is reported that stationarity rather than motion can be perceived for displaced stimuli, not because of insufficient motion energy for the stimulus to activate individual motion detectors, but because of cooperative interactions that actively suppress the perception of motion. A long row of evenly spaced dots was presented in counterphase; the dots presented during each 180 ms frame were located midway between the dots presented during the previous frame. When either a blank interval as brief as 15 ms was inserted between successive frames or the luminance polarity of the dots was reversed on successive frames, the unidirectional motion pattern perceived for small interdot distances (small displacements) was replaced by the perception of stationarity. However, when under the same conditions a single dot was displaced over the same small distances, motion rather than stationarity was perceived. The contrasting results for the long row of displaced dots and the single displaced dot indicated that when the activation of motion detectors is weakened (by nonzero interframe intervals and/or the reversal of luminance polarity), the perception of motion can be actively suppressed by the collective effects of inhibitory interactions among the large ensemble of detectors that is activated by the long row of dots.

Field Dependence-Independence↗
PubMed1998

Evocation and characterization of percepts of apparent motion on the face.

The percepts evoked by sequential stimulation of sites in close spatial proximity (< or = 2.5 cm) on the face were studied. Both method-of-limits and magnitude-estimation procedures were used to identify and characterize alterations in the percepts produced by systematic changes in the temporal and spatial parameters of the sequence. Each site was stimulated by a vertically oriented row of miniature vibrating probes. Apparent motion was consistently perceived when the delay between the onsets of sequentially activated rows (interstimulus onset interval, or ISOI) fell within a relatively narrow range of values, the lower limit of which approximated 5 msec. Both the upper limit and the perceived smoothness and continuity of the motion percepts (goodness of motion) increased with the duration for which each row stimulated the skin over the range evaluated, 15-185 msec. For the successive activation of only two rows, goodness of motion was not influenced by changes in their separation from 0.4 to 2.5 cm. The ISOI values at which magnitude estimates of goodness of motion were highest increased with the duration for which each row stimulated the skin. As such, maximum goodness of motion decreased with increases in the apparent velocity of motion. When the number of sequentially activated rows was increased from two to four or more, the quality of the motion percepts improved. For the successive activation of multiple closely spaced rows, values of ISOI at which numerical estimates of goodness of motion were highest approximated integral fractions of the duration for which each row stimulated the skin. In this situation, the probes rose and fell in a regular, step-locked rhythm to simulate an edge-like or rectangular object moving across the skin. The goodness of motion so attained was relatively independent of the apparent velocity of motion.

Adult↗
PubMed1995

Visual perception. Seeing motion signals in noise.

The brain can integrate local motion signals among noise to gain a global perception of visual motion. The scope and limits of this ability may reveal how the inputs to central motion systems are organized.

Animals↗
PubMed1989

Motion processing by chromatic and achromatic visual pathways.

We describe a family of stimuli consisting of colored bars of different orientations, which, when presented in rapid succession, may elicit unambiguous motion perception. These stimuli permitted the isolation of directional spatiotemporal information extracted from oriented luminance clues, from nonoriented chromatic-plus-luminance clues, or, when the stimuli were presented under equiluminant conditions, from pure chromatic clues. As a general rule, matching of orientation induces weaker motion-detection performances than does matching of color. When the orientation clues are in competition with the chromatic ones, motion perception based on the former is always overridden by motion perception based on the latter. We indirectly isolated an oriented chromatic mechanism that also contributes to motion perception. We finally showed that, under equiluminant conditions, matching of orientation across different colors is inefficient in eliciting motion perception, either because motion information is extracted poorly across different chromatic channels or because such channels show little orientational selectivity. Because motion strength determined by each of the manipulated attributes follows different functions with the displacement (or velocity) of the stimuli, we propose the existence of three underlying mechanisms, a luminance mechanism, a chromatic-plus-luminance mechanism, and a pure chromatic mechanism, each of which provides motion information.

Attention↗
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↗
PubMed2001

Visual motion and the human brain: what has neuroimaging told us?

Recently, neuroimaging techniques have been applied to the study of human motion perception, complementing established techniques such as psychophysics, neurophysiology and neuropsychology. Because vision, particularly motion perception, has been studied relatively extensively, it provides an interesting case study to examine the contributions and limitations of neuroimaging to cognitive neuroscience. We suggest that in the domain of motion perception neuroimaging has: (1) revealed an extensive network of motion areas throughout the human brain, in addition to the well-studied motion complex (MT+); (2) verified and extended findings from other techniques; (3) suggested extensive top-down influences on motion perception; and (4) allowed experimenters to examine the neural correlates of awareness. We discuss these contributions, along with limitations and future directions for the neuroimaging of motion.

Attention↗
PubMed1999

Abnormal depth perception from motion parallax in amblyopic observers.

Many similarities exist between the perception of depth from binocular stereopsis and that from motion parallax. Moreover, Rogers (1984, cited in, Howard, I. P., & Rogers, B. J. (1995). Binocular vision and stereopsis. Oxford Claridon, New York.) suggests a relationship between an observer's ability to use disparity information and motion parallax information in a depth perception task. To more closely investigate this relationship, depth perception was studied in normal observers and amblyopic observers with poor stereo vision. As expected, amblyopic observers performed much worse than normal observers on depth discriminations requiring use of binocular disparity. However, amblyopic observers also performed much worse than normal observers on depth discriminations based on motion parallax. This result provides supporting evidence for a psychoanatomical link between the perception of depth from motion and the perception of depth from binocular disparity.

Amblyopia↗
PubMed1996

Simulating self-motion.

In general, vehicle motions far exceed the mechanical constraints of an earth-fixed simulator base. Inertial motions can, therefore, only be simulated in partial agreement with those of the actual vehicle. As a consequence, physical mismatches between inertial and environmental motion are inevitable. Here, the concept of a subjective reference frame is introduced, relative to which perceived self-motion is defined. This frame must be released from the earth-fixed frame to evoke simulated self-motion. In addition, self-motion and environmental motion need to be perceived reciprocal, in order to evoke a stationary perceived environment. Due to the only limited accuracy of human self-motion perception, however, perceived self-motion and perceived environmental motion need not to be exactly reciprocal. The extent to which self-motion and environmental motion may differ can be expressed by a just noticeable difference. This just noticeable difference denotes the threshold at which the environment is perceived to move. In this article, a self-motion perception model is outlined in which perceived environmental motion and perceived self-motion are separated. The perception model and the just noticeable differences can then be applied to determine the inertial stimulation that is needed to evoke perceived self-motion, in which the environment is perceived stationary throughout simulation.

Humans↗
PubMed1997

False perception of motion in a patient who cannot compensate for eye movements.

We are usually unaware of the motion of an image across our retina that results from our own movement. For instance, during slow-tracking eye movements we do not mistake the shift of the image projected onto the retina for motion of the world around us, but instead perceive a stable world. Following early suggestions by von Helmholtz, it is commonly believed that this spatial stability is achieved by subtracting the retinal motion signal from an internal reference signal, such as a copy of the movement command (efference copy). Object motion is perceived only if the two differ. Although this concept is widely accepted, its anatomical underpinning remains unknown. Here we describe the case of a patient with bilateral extrastriate cortex lesions, suffering from false perception of motion due to an inability to take eye movements into account when faced with self-induced retinal image slip. This is indicated by the fact that during smooth-pursuit eye movements, he perceives motion of the stationary world at a velocity that corresponds to the velocity of his eye movement; that is, he perceives the raw retinal image slip uncorrected for his own eye movements. We suspect that this deficiency reflects damage of a distinct parieto-occipital region that disentangles self-induced and externally induced visual motion by comparing retinal signals with a reference signal encoding eye movements and possibly ego-motion in general.

Adult↗
PubMed1997

Dynamic, state-dependent thresholds for the perception of single-element apparent motion: bistability from local cooperativity.

Previous studies have indicated that the formation of coherent patterns for multielement motion displays depends on global cooperative interactions among large ensembles of spatially distributed motion detectors. These interactions enhance certain motion directions and suppress others. It is reported here that perceiving one element moving between two nearby locations likewise is subject to cooperative influences (possibly facilitating and inhibiting interactions within a local ensemble of overlapping detectors). Thresholds depending on luminance contrast were measured for a generalized single-element apparent-motion stimulus, and evidence for spontaneous switching and hysteresis effects indicated that motion perception near the 50% threshold was bistable. That is, for conditions in which motion and nonmotion were perceived half the time, the two percepts were distinct; when one was perceived, it clearly was discriminable from the other. These results indicated that (1) single-element apparent-motion thresholds depended on the immediately preceding state of the ensemble of motion detectors responding to the stimulus, and (2) the stimulus activation of individual motion detectors always might be influenced by recurrent, cooperative interactions resulting from the detectors' being embedded within interconnected ensembles.

Adult↗
PubMedDate not supplied

Visual performance and recovery in recently detoxified alcoholics.

In order to assess the impact of chronic alcohol misuse on basic visual functions, we investigated motion perception, visual short-term memory, and visual divided attention in recently detoxified patients and matched controls by means of visual psychophysical tasks. Subjects were tested twice within the first 3 weeks of detoxification in order to assess the potential recovery of visual performance. Patients demonstrated significant impairments in visual perception of coherent motion for slow, but not faster, speeds, and in speed discrimination as assessed by random dot kinematograms. Visual short-term memory tested with a delayed vernier discrimination task, on the other hand, was not significantly affected in patients. When processing hierarchical letters, a divided attention task, detoxified patients showed neither impairments in overall attentional capacity nor attentional allocation, but slightly enhanced interference of global information on local target processing. The results of the visual divided attention task contradict the predictions of the 'right hemisphere' hypothesis of alcoholism: global target information - mediated by the right hemisphere - was not only accessible to detoxified patients, but seemed to exert an even greater influence on local processing during early detoxification, than in matched controls. Limited recovery within the first 3 weeks was seen only in visual speed discrimination. Recently detoxified patients revealed deficits similar to intoxicated social drinkers in identical tests of visual perception of motion, but not visual short-term memory.

Adult↗
PubMed2006

Aging and visual motion discrimination in normal adults and schizophrenia patients.

Motion perception is impaired in many neuropathological conditions, including schizophrenia. Motion perception also declines in the course of normal aging. In this study, we ask whether aging is an additive factor in the motion-discrimination deficits of schizophrenia patients. We examined motion perception in schizophrenia patients (n=44) and non-psychiatric controls (n=40) whose ages ranged from 18 to 55. The tasks included velocity discrimination and contrast detection. Thresholds for each of the two tasks were determined for each subject using psychophysical methods. Schizophrenia patients showed significantly increased thresholds (degraded performance) for velocity discrimination compared with the controls. Degraded performance in patients was not related to age. In controls, however, velocity discrimination thresholds were significantly increased beginning by age 45. Performance on a contrast-detection task, which does not require precise discrimination of motion signals, was not significantly affected by age in either group. Aging, even in its early stages, degrades motion discrimination in normal adults. Aging, however, does not adversely affect motion-discrimination deficits in schizophrenia patients through age 55. A similar motion-discrimination deficit in schizophrenia patients and aging normal adults suggests that the mechanisms underlying motion processing in schizophrenia and normal aging may be associated.

Acceleration↗
PubMed1997

Perceptual grouping in space and time: evidence from the Ternus display.

We report three experiments investigating the effect of perceptual grouping on the appearance of a bistable apparent-motion (Ternus) display. Subjects viewed a Ternus display embedded in an array of context elements that could potentially group with the Ternus elements. In contrast to several previous findings, we found that grouping influenced apparent motion perception. In Experiment 1, apparent motion perception was significantly affected via grouping by shape similarity, even when the visible persistence of the elements was controlled. In Experiment 2, elements perceived as moving without context were perceived as stationary without context were perceived as moving when grouped with moving elements perceived as stationary without context were perceived as moving when grouped with moving context elements. We argue that grouping in the spatial and temporal domains interact to yield perceptual experience of apparent-motion displays.

Adult↗