Space: from perception to action.
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Humans↗
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Results for “Space Perception”
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The time of consciousness and vice versa.
The temporal granularity of consciousness may be far less fine than the real-time information processing mechanisms that underlie our sensitivity to small temporal differences. It is suggested that conscious time perception, like space perception, is subject to errors that belie a unitary underlying representation. E. R. Clay's (The Alternative: A Study in Psychology, 1882) concept of the "specious present," an extended moment represented in consciousness, is suggested as an alternative to the more common notion of instantaneous experience that underlies much reasoning based on the "time of arrival" in consciousness.
Chronobiology Phenomena↗
[The resting EEG in relation to neurovegetative status and spatial perception in normal young adults (author's transl)].
The relationship between measurable EEG-parameters and an index of irritability of the autonomous system was examined. The data consisted of the resting EEGs of 488 adult students, 290 male and 198 female. Time-domain analysis was used for computerized evaluation. Females showed a significantly higher average autonomous irritability index than males. Moreover, positive correlations were found between this index and the number of occipital beta-waves; the correlation with number of alpha-waves was negative. Amplitudes tend to be correlated negatively with the index; most correlations are stronger in females than in males. In 73 proband, 35 male and 43 female,--carriers of various inherited EEG-variants and age- and sex-matched controls,--spatial perception was examined by the WU-subtest of the "Intelligenzstrukturtest" (Amthauer). Males showed significantly higher average test values than females, and in women, a significant relationship between occipital EEG and space perception was found. There appears to be a positive association between space perception and amplitude of occipital alpha- and beta-waves. On the other hand, however, carriers of the typical low-voltage EEG show very good space perception despite their low amplitudes of occipital alpha- and beta-waves.
Adult↗
Meridional size disparity as a function of compressed inferior visual space: a case in point.
This case report describes a very unusual form of aniseikonia which was eventually documented to be variable within the total field of vision and limited to vertical space perception. Initially the condition could be partially relieved by monocular occlusion, visual training procedure, and the use of isoikonic lenses. Ultimately, the greatest improvement was produced by the introduction of prismatic properties to the lenses which directly addressed the patient's problem of meridional space perception.
Aniseikonia↗
Properties of the internal representation of gravity inferred from spatial-direction and body-tilt estimates.
One of the key questions in spatial perception is whether the brain has a common representation of gravity that is generally accessible for various perceptual orientation tasks. To evaluate this idea, we compared the ability of six tilted subjects to indicate earth-centric directions in the dark with a visual and an oculomotor paradigm and to estimate their body tilt relative to gravity. Subjective earth-horizontal and -vertical data were collected, either by adjusting a visual line or by making saccades, at 37 roll-tilt angles across the entire range. These spatial perception responses and the associated body-tilt estimates were subjected to a principal-component analysis to describe their tilt dependence. This analysis allowed us to separate systematic and random errors in performance, to disentangle the effects of task (horizontal vs. vertical) and paradigm (visual vs. oculomotor) in the space-perception data, and to compare the veridicality of space perception and the sense of self-tilt. In all spatial-orientation tests, whether involving space-perception or body-tilt judgments, subjects made considerable systematic errors which mostly betrayed tilt underestimation [Aubert effect (A effect)] and peaked near 130 degrees tilt. However, the A effect was much smaller in body-tilt estimates than in spatial pointing, implying that the underlying signal processing must have been different. Pointing results obtained with the visual and the oculomotor paradigm were not identical either, but these differences, which were task-related (horizontal vs. vertical), were subtle in comparison. The tilt-dependent pattern of random errors (noisy scatter) was almost identical in visual and oculomotor pointing results, showing a steep monotonic increase with tilt angle, but was again clearly different in the body-tilt estimates. These findings are discussed in the context of a conceptual model in an attempt to explain how the different patterns of systematic and random errors in external-space and self-tilt perception may come about. The scheme proposes that basically similar computational mechanisms, working with different settings, may be responsible.
Adult↗
Cortical representation of visual three-dimensional space.
Perception of real depth includes information on stereopsis and distance. How both interact in the visual pathway was the subject of a study performed on the behaving monkey. Neurons in the primary visual cortex (area V1) have their activity, visual and/or spontaneous, modulated by the viewing distance. Disparity selectivity may be present or better expressed at a given viewing distance. This modulation is independent of the visual pattern. The use of prisms shows that vergence is implicated in this phenomenon. Consequently, extraretinal signals related to ocular motility have access to area V1. Among them, proprioceptive signals from the eye muscles have been shown to be involved in visual cortical function and in the development of depth perception. It is possible that the same signals may also be involved in the distance modulation shown in V1 neurons, but this remains to be examined. A possible specialisation of disparity-selective cells in different cortical areas is discussed.
Animals↗
Disorders in perception of space due to lesions of the nervous system.
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Brain Neoplasms↗
Quantification of reaction time and time perception during Space Shuttle operations.
A microprocessor-based test battery containing simple reaction time, choice reaction time, and time perception tasks was flown aboard a 1985 Space Shuttle flight. Data were obtained from four crewmembers. Individual subject means indicate a correlation between change in reaction time during the flight and the presence of space motion sickness symptoms. The time perception task results indicate that the shortest duration task time (2 s) is progressively overestimated as the mission proceeds and is statistically significant (p less than 0.01) when comparing preflight and postflight baselines. The tasks that required longer periods of time to estimate (8, 12, and 16 s) are less affected.
Analysis of Variance↗
Some aspects of auditory space, speech perception and the use of hearing aids.
The auditory space of an individual is operationally defined as that perceptual area that lies between the upper tolerance level for loud sounds and the threshold of hearing for a specified range of frequencies. Results from recent experimental work are presented to show a difference of some 15 dB between comfortable listening level and loudness discomfort-level, up to 80 dB hearing loss. Results are also shown for the measurement of reaction time to a 2AFC task testing the ability to discriminate initial consonants. Loudness scaling is suggested as a method of eliciting supra-threshold measurements which might be helpful in the fitting of hearing aids.
Audiometry, Speech↗
Illusory perceptions of space and time preserve cross-saccadic perceptual continuity.
When voluntary saccadic eye movements are made to a silently ticking clock, observers sometimes think that the second hand takes longer than normal to move to its next position. For a short period, the clock appears to have stopped (chronostasis). Here we show that the illusion occurs because the brain extends the percept of the saccadic target backwards in time to just before the onset of the saccade. This occurs every time we move the eyes but it is only perceived when an external time reference alerts us to the phenomenon. The illusion does not seem to depend on the shift of spatial attention that accompanies the saccade. However, if the target is moved unpredictably during the saccade, breaking perception of the target's spatial continuity, then the illusion disappears. We suggest that temporal extension of the target's percept is one of the mechanisms that 'fill in' the perceptual 'gap' during saccadic suppression. The effect is critically linked to perceptual mechanisms that identify a target's spatial stability.
Adult↗
Effects of illusory spatial anisometry in unilateral neglect.
Patients with visuospatial neglect tend to underestimate horizontal magnitudes in contralesional space. It has been recently hypothesised that this behaviour might be due to anisometry of space perception, by which horizontal stimuli would be progressively underestimated proceeding from the ipsi towards the contralesional side of space. We investigated the effects of modulating space perception through the Oppel-Kundt illusion (i.e. a filled space is perceived as more expanded than an empty space) on the behaviour of 28 neglect patients and 28 normal subjects. The two groups bisected lines on backgrounds of vertical lines evenly spaced or unevenly spaced, with distances which decreased progressively from one side of the page to the other. On the same backgrounds, they extended segments to the left or to the right so as to double them. Patients also had to cancel targets, the density of which was evenly distributed or horizontally increased from one side of the page to the other. Both groups were prone to the illusion. Neglect bias was modulated by the illusion in the expected direction. It was reduced when the illusion induced a perceptual distortion opposite to that thought to underlie neglect. On bisection and cancellation tasks, illusory effects were greater in patients with higher values of response bias on the Milner Landmark task. These findings, taken together with patients' anatomical data, suggest that a modulation of neglect through a visual illusion can normally be induced in patients with relatively intact visual input processes.
Aged↗
Selective deficit of auditory localisation in patients with visuospatial neglect.
Possible auditory deficits in neglect were examined by comparing the performance of four right brain-damaged (RBD) patients with left visuospatial neglect, versus four RBD patients without neglect, in three auditory tasks. The first task required speeded discrimination of sound elevation, by moving a central lever up or down according to the vertical position of a peripheral target sound, regardless of its side. The other two auditory tasks were non-spatial, requiring either speeded pitch discrimination (moving the central lever up for high pitch, down for low pitch) or speeded target detection. Neglect patients' performance was impaired with respect to RBD controls only when the auditory task required spatial coding of the target sound (the up/down spatial discrimination). This demonstrates a selective deficit of auditory space perception in neglect patients. This auditory spatial deficit was more pronounced for left than right sounds. Since auditory space perception was impaired in the vertical dimension, the observed deficit cannot be attributed to a systematic rightward shift in sound localisation. Instead, the results suggest increased spatial uncertainty in sound localisation by neglect patients, particularly for auditory targets on the contralesional side. These findings are related to multimodal coding of space in the parietal cortex, which was damaged in the neglect patients, but not in the RBD controls.
Adult↗
Flicker distorts visual space constancy.
Effects of flicker on space perception were measured by displacing a flickering target during saccadic eye movements. A small target was flickered at 33, 66, 130 or 260 Hz. Using a 2-interval forced-choice design, sensitivity to the displacement was about twice as great when the target was moved in the direction opposite the eye movement as when it was moved in the same direction. This would be expected from a partial breakdown of space constancy--the world should seem to jump in the direction opposite an eye movement. Even if a suppression of displacement detection during saccades prevents this jump from being perceived; it should be easier to detect a target displacement in the direction opposite the eye movement than in the same direction: when movement is opposite, the imposed displacement adds to the illusory displacement, making detection easier. Displacements were more easily detected at lower flicker rates. Results imply that both masking and extraretinal signals are important in suppressing the detectability of target displacements during saccades, and that flicker on video display terminals may distort space perception.
Humans↗
Simulating and testing visual exploration in spatial neglect based on a new model for cortical coordinate transformation.
Most studies of object and space perception have focused on neural representations of either object-centered or egocentric coordinate systems. But daily life requires interactions of both kinds of coordinates. We have recently proposed an 'integrated space-object (ISO-) map' combining both coordinate systems in one representation. Based on a lesioned version of this model, here we present results from visual search simulations demonstrating that the model accounts for contralesional neglect during space-centered and object-centered exploration tasks. Interestingly, the model simulations also predicted an amelioration of neglect symptoms during exploration with more ipsilesional object positions. By measuring the eye movements of neglect patients during different exploratory tasks, we confirmed all model predictions. These results corroborate the view that the brain might combine coordinates for object and space perception in an integrated coordinate system as suggested by the ISO-map model.
Aged↗
Studies in visual perception of architectural spaces and rooms. V. Aesthetic preferences.
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Adolescent↗
Perception of visual space at the time of pro- and anti-saccades.
The localization of peri-saccadically flashed objects shows two types of errors: first, a uniform shift in saccade direction, and second, a compression of visual space around the saccade target. Whereas the uniform shift occurs when the experiment is performed in complete darkness compression occurs when additional visual references are available. Thus peri-saccadic mislocalization contains motor and visual components. To distinguish between both factors we compared peri-saccadic localization errors during pro- and anti-saccades. In the case of anti-saccades, the visual cue that elicits the saccade and the actual eye movement are in opposite directions. We asked whether peri-saccadic compression can be observed with anti-saccades, and if so, whether the compression is directed toward the visual cue or follows the actual eye movement. In blocked trials, subjects performed saccades either toward a visual cue (pro-saccade) or to the mirrored position opposite to a visual cue (anti-saccade). Peri-saccadically, we flashed a thin vertical bar at one of four possible locations. Subjects had to indicate the perceived position of the bar with a mouse pointer about 500 ms after the saccade. Experiments were performed in complete darkness and with visual references. Peri-saccadic mislocalizations occurred during anti-saccades. The mislocalizations were very similar for pro- and anti-saccades in magnitude and direction. For both, pro- and anti-saccades, mislocalizations were directed toward the actual eye movement and not the visual cue.
Adult↗
Monocular geometry is selectively distorted in the central visual field of strabismic amblyopes.
Strabismic amblyopia is associated with a distorted perception of visual space. The aim of our study was to investigate the monocular space perception of strabismic observers at several locations in the central and peripheral visual field. We tested nine observers with strabismic and/or anisometropic amblyopia, two strabismic subjects with alternating fixation and two normal control subjects. The task was to align a light stimulus with two vertically arranged reference marks. Testing conditions included three separations of the references along the vertical meridian (10 degrees, 20 degrees and 40 degrees) as well as several presentation sites of the vertical references in the nasal and temporal peripheral visual field (5 degrees, 10 degrees and 20 degrees from fixation). Performance with the amblyopic eye was clearly impaired as compared to the nonamblyopic eye. For alignment along the vertical meridian, all amblyopic eyes showed increased uncertainty in their position judgements. Most of the squinting eyes of amblyopes also displayed a systematic lateral displacement of the test stimulus in relation to the reference marks, in the most extreme case up to almost 7 degrees. Usually, larger errors were found with wider separations of the reference marks. In the peripheral field, the differences between the amblyopic and the nonamblyopic eye diminished or disappeared. Thus, monocular geometry appears to be selectively impaired in the central visual field of the deviated eye of strabismic amblyopes. These spatial distortions might be related to the different states of binocular correspondence in the central vs. peripheral visual field, shown by some strabismic amblyopes.
Amblyopia↗
[The role of the first and second signal systems in the correlation of semantic and perceptive color spaces].
The first and the second signal systems were studied in computerized experiments using colour stimuli and colour names. Multidimensional graduation of subjective differences between monochromatic colours and colour names showed that perceptual colour space and semantic colour space were isomorphic and constituted hyperspheres in a four-dimensional space. The angles of the hypersphere corresponded to hue, lightness, and saturation of colours and ordered colour names with respect to these characteristics. The subjective differences between monochromatic colours and colour names made it possible to construct a common space where monochromatic colours and corresponding colour names were represented by the neighbouring points, thus supporting isomorphic relations between perceptual and semantic colour spaces.
Color Perception↗