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Results for “spatial dependency”

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PubMed1996

Spatio-temporal requirements for binocular correlation in stereopsis.

We measured sensitivity to binocular correlation in dynamic random-dot stereograms that defined moving sinusoidal gratings-in-depth. At a range of spatial frequencies and drift rates we established sensitivity by adding Gaussian distributed disparity noise to the modulation of disparity that defined a cyclopean grating, and finding the noise amplitude that rendered the grating just detectable. This permitted correlation thresholds to be measured at a range of suprathreshold disparity amplitudes. Spatial requirements for binocular correlation depend little on temporal frequency, and vice versa. This suggests that binocular correlation mechanisms can be characterized by independent spatial and temporal sensitivity functions. The temporal frequency function has a low pass characteristic. Sensitivity declines above about 1 c/sec, reaching its limit at 4-8 c/sec. The spatial characteristic depends greatly on the amplitude of disparity modulation, changing from band pass at low amplitude to low pass at high amplitude. The maximum resolvable spatial frequency is 4-6 c/deg, but declines sharply for relatively high amplitudes. The interaction between amplitude and spatial frequency cannot be explained by fixed high or low limits on detectable disparity gradients.

Depth Perception↗

PubMed2005

The inositol polyphosphate 5-phosphatase, PIPP, Is a novel regulator of phosphoinositide 3-kinase-dependent neurite elongation.

The spatial activation of phosphoinositide 3-kinase (PI3-kinase) signaling at the axon growth cone generates phosphatidylinositol 3,4,5 trisphosphate (PtdIns(3,4,5)P3), which localizes and facilitates Akt activation and stimulates GSK-3beta inactivation, promoting microtubule polymerization and axon elongation. However, the molecular mechanisms that govern the spatial down-regulation of PtdIns(3,4,5)P3 signaling at the growth cone remain undetermined. The inositol polyphosphate 5-phosphatases (5-phosphatase) hydrolyze the 5-position phosphate from phosphatidylinositol 4,5 bisphosphate (PtdIns(4,5)P2) and/or PtdIns(3,4,5)P3. We demonstrate here that PIPP, an uncharacterized 5-phosphatase, hydrolyzes PtdIns(3,4,5)P3 forming PtdIns(3,4)P2, decreasing Ser473-Akt phosphorylation. PIPP is expressed in PC12 cells, localizing to the plasma membrane of undifferentiated cells and the neurite shaft and growth cone of NGF-differentiated neurites. Overexpression of wild-type, but not catalytically inactive PIPP, in PC12 cells inhibited neurite elongation. Targeted depletion of PIPP using RNA interference (RNAi) resulted in enhanced neurite differentiation, associated with neurite hyperelongation. Inhibition of PI3-kinase activity prevented neurite hyperelongation in PIPP-deficient cells. PIPP targeted-depletion resulted in increased phospho-Ser473-Akt and phospho-Ser9-GSK-3beta, specifically at the neurite growth cone, and accumulation of PtdIns(3,4,5)P3 at this site, associated with enhanced microtubule polymerization in the neurite shaft. PIPP therefore inhibits PI3-kinase-dependent neurite elongation in PC12 cells, via regulation of the spatial distribution of phospho-Ser473-Akt and phospho-Ser9-GSK-3beta signaling.

Animals↗

PubMed1991

Peripheral spatial vision: limits imposed by optics, photoreceptors, and receptor pooling.

We examined the contribution of optical and photoreceptor properties as well as receptor pooling to eccentricity-dependent variations in spatial vision by comparing the performance of ideal observers with that of human observers. We measured contrast sensitivity functions in human observers and calculated such functions in ideal observers for retinal eccentricities of 0-40 deg. Comparisons of human and ideal performance in a variety of tasks reveal that many aspects of the variation in spatial vision with eccentricity can be understood from an analysis of the discrimination information available at the retinal ganglion cells.

Contrast Sensitivity↗

PubMed1980

Spatial characteristics of movement detection mechanisms in human vision. I. Achromatic vision.

Threshold illumination levels, It, for visual detection of white light targets, moving across spatially structured background fields, have been measured and it is shown that, for a given background illumination level, It depends upon the spatial characteristics of the background field structure. Thus, with the background composed of a square-waveform grating of fundamental spatial frequency f cycles/deg, It is maximum for an intermediate value of f, and falls as f increases or decreases from this value. The relationship between It and f characterizes the interaction between movement detection and the background grating, and is designated the IMG function. The parametric properties of the IMG functions are described and it is established that the mechanisms which give rise to these functions are sensitive to the movement, but not the spatial structure of the target. They correspond, therefore, to the movement-sensitive Y-type mechanisms, observed in electrophysiological studies of cat and primate visual pathways. The spatial distribution of sensitivity associated with the IMG functions has been computed by 2-D transform methods, the computation yielding circularly symmetric, centre-surround antagonistic "receptive field" distributions.

Adult↗

PubMed1985

Contrast detection and detection of contrast modulation for noise gratings.

Threshold contrast was measured for noise gratings of various spatial frequency bandwidths and central frequencies. The results indicate that the contrast reaches threshold whenever the spatial power of the stimulus, filtered according to the contrast sensitivity function, exceeds a fixed level, irrespective of the width of the spatial frequency range over which the power is distributed. No "critical band effect" is found. For suprathreshold noise gratings of various bandwidths we measured thresholds for the detection of sinusoidal (amplitude) modulation of the contrast. The results indicate that the visual system uses the spatial power always with about the same efficiency, irrespective of the bandwidth over which it is distributed. The thresholds depend on the spatial frequency of the modulation: the visual system appears to be unable to use information from more than one cycle of the modulation frequency.

Humans↗

PubMed2003

Near-field measurement of short-range correlation in optical waves transmitted through random media.

Two-dimensional near-field images of speckle patterns formed by optical waves transmitted through a disordered porous silica glass sample are measured. The corresponding 2D intensity correlation function, C, is extracted. The subwavelength spatial resolution of near-field microscopy allows us to resolve in the spatial distribution of C the expected subwavelength oscillations and to follow their dependence on the excitation wavelength. Finally, we deduce the effective refractive index of the material by fitting the theoretical spatial dependence of C to our experimental results.

Light↗

PubMed1990

Spatial and temporal analysis of calcium-dependent electrical activity in guinea pig Purkinje cell dendrites.

We have used the calcium indicator dye arsenazo III, together with a photodiode array, to record intracellular calcium changes simultaneously from all regions of individual guinea pig cerebellar Purkinje cells in slices. The optical signals, recorded with millisecond time resolution, are good indicators of calcium-dependent electrical events. For many cells the sensitivity of the recordings was high enough to detect signals from each array element without averaging. Consequently, it was possible to use these signals to follow the complex spatial and temporal patterns of plateau and spike potentials. Calcium entry corresponding to action potentials was detected from all parts of the dendritic field including the fine spiny branchlets, demonstrating that calcium action potentials spread over the entire arbor. Usually, the entire dendritic tree fired at once. But sometimes only restricted areas had signals at any one moment with transients detected in different regions at other times. In one cell, six separate zones were distinguished. These results show that calcium action potentials could be regenerative in some dendrites and could fail to propagate into others. Signals from plateau potentials were also detected from extensive areas in the dendritic field but were always smaller than those caused by a burst of action potentials.

Action Potentials↗

PubMed1997

Spatial memory is related to hippocampal subcellular concentrations of calcium-dependent protein kinase C isoforms in young and aged rats.

Relationships were examined between spatial learning and hippocampal concentrations of the alpha, beta2, and gamma isoforms of protein kinase C (PKC), an enzyme implicated in neuronal plasticity and memory formation. Concentrations of PKC were determined for individual 6-month-old (n = 13) and 24-month-old (n = 27) male Long-Evans rats trained in the water maze on a standard place-learning task and a transfer task designed for rapid acquisition. The results showed significant relationships between spatial learning and the amount of PKC among individual subjects, and those relationships differed according to age, isoform, and subcellular fraction. Among 6-month-old rats, those with the best spatial memory were those with the highest concentrations of PKCgamma in the particulate fraction and of PKCbeta2 in the soluble fraction. Aged rats had increased hippocampal PKCgamma concentrations in both subcellular fractions in comparison with young rats, and memory impairment was correlated with higher PKCgamma concentrations in the soluble fraction. No age difference or correlations with behavior were found for concentrations of PKCgamma in a comparison structure, the neostriatum, or for PKCalpha in the hippocampus. Relationships between spatial learning and hippocampal concentrations of calcium-dependent PKC are isoform-specific. Moreover, age-related spatial memory impairment is associated with altered subcellular concentrations of PKCgamma and may be indicative of deficient signal transduction and neuronal plasticity in the hippocampal formation.

Aging↗

PubMed1999

Haptic perception of linear extent.

The perception of linear extent in haptic touch appears to be anisotropic, in that haptically perceived extents can depend on the spatial orientation and location of the object and, thus, on the direction of exploratory motion. Experiments 1 and 2 quantified how the haptic perception of linear extent depended on the type of motion (radial or tangential to the body) when subjects explored different stimulus objects (raised lines or solid blocks) varying in length and in relative spatial location. Relatively narrow, shallow, raised lines were judged to be longer, by magnitude estimation, than solid blocks. Consistent with earlier reports, stimuli explored with radial arm motions were judged to be longer than identical stimuli explored with tangential motions; this difference did not depend consistently on the lateral position of the stimulus object, the direction of movement (toward or away from the body), or the distance of the hand from the body but did depend slightly on the angular position of the shoulder. Experiment 3 showed that the radial-tangential effect could be explained by temporal differences in exploratory movements, implying that the apparent anisotropy is not intrinsic to the structure of haptic space.

Adolescent↗

PubMed2002

Biomechanical effects of intraspecimen variations in tissue modulus for trabecular bone.

Although recent nanoindentation studies have revealed the existence of substantial variations in tissue modulus within single specimens of trabecular bone, little is known regarding the biomechanical effects of such intraspecimen variations. In this study, high-resolution finite element modeling was used to investigate these effects. With limited literature information on the spatial distribution of intraspecimen variations in tissue modulus, two plausible spatial distributions were evaluated. In addition, three specimens (human femoral neck, human vertebral body, and bovine proximal tibia) were studied to assess the role of trabecular architecture. Results indicated that for all specimen/distribution combinations, the apparent modulus of the whole specimen decreased nonlinearly with increasing coefficient of variation (COV) of tissue modulus within the specimen. Apparent modulus decreased by <4% when tissue modulus COV was increased from 0% to 20% but decreased by 7-24%, depending on the assumed spatial distribution, for an increase in tissue modulus COV from 20% to 50%. For compressive loading to the elastic limit, increasing tissue modulus COV from 20% to 50% caused up to a 28-fold increase in the amount of failed tissue, depending on assumed spatial distribution and trabecular architecture. We conclude that intraspecimen variations in tissue modulus, if large, may have appreciable effects on trabecular apparent modulus and tissue-level failure. Since the observed effects depended on the assumed spatial distribution of the tissue modulus variations, a description of such distributions, particularly as a function of age, disease, and drug treatment, may provide new insight into trabecular bone structure-function relationships.

Adult↗

PubMed1998

A neurological dissociation between preserved visual and impaired spatial processing in mental imagery.

Studies on primates have shown that visual and spatial perceptual analysis depends on two separate neural pathways, associated with the processing of "what" and "where" an object is (visual characteristics and spatial coordinates, respectively). Similar dichotomies have been proposed by cognitive psychologists (e.g., the contrast between visual and spatial processing in working memory) and by neuropsychologists (e.g., the distinction between topographic agnosia and amnesia). In this paper we report the case of a patient with a severe spatial disorientation whose perceptual processing of visual and spatial information was normal, but in imagery tasks she had a dissociation between preserved visual and impaired spatial processing. While her ability to represent objects visually was intact, she failed in any task requiring mental rotation, recall of spatial position or execution of spatially based imagery operations. The case clearly demonstrates that visual and spatial imagery are functionally independent processes which must rely on different underlying neural systems. This pattern of impairment also explains the associated topographical amnesia as an inability to integrate spatial information in a mental map.

Aged↗

PubMed2005

Determination of the optimum sampling frequency of noisy images by spatial statistics.

In optical metrology the final experimental result is normally an image acquired with a CCD camera. Owing to the sampling at the image, an interpolation is usually required. For determining the error in the measured parameters with that image, knowledge of the uncertainty at the interpolation is essential. We analyze how kriging, an estimator used in spatial statistics, can generate convolution kernels for filtering noise in regularly sampled images. The convolution kernel obtained with kriging explicitly depends on the spatial correlation and also on metrological conditions, such as the random fluctuations of the measured quantity, and the resolution of the measuring devices. Kriging, in addition, allows us to determine the uncertainty of the interpolation, and we have analyzed it in terms of the sampling frequency and the random fluctuations of the image, comparing it with Nyquist criterion. By use of kriging, it is possible to determine the optimum-required sampling frequency for a noisy image so that the uncertainty at interpolation is below a threshold value.

Journal Article↗

PubMed1984

The role of pattern and flicker mechanisms in determining the spatiotemporal limits of velocity perception. 1. Upper movement thresholds.

For rapidly moving gratings, the percept of smooth drift is limited by the "coherent drift' threshold. At more rapid rates of movement, the spatial and temporal structure of the stimulus may be individually perceived, but the global spatiotemporal percept of smooth drift breaks down and the stimulus appears to be made up of discrete patches of flickering grating. This coherent drift threshold is strongly dependent upon both spatial frequency and contrast and roughly parallels the "pattern', rather than the "flicker' threshold. The relationships between the three types of threshold suggest that the global percept of smooth drift depends upon mechanisms which are the same as those which underpin the separate percepts of spatial and temporal structure.

Flicker Fusion↗

PubMed2004

Orientation and perspective dependence in route and survey learning.

Three experiments investigated the role of egocentric orientation in subsequent memory for layouts learned via route (ground-level) and survey (aerial or overview) perspectives. Participants learned virtual environments from text descriptions (Experiment 1) or visual presentation (Experiments 1-3). In all experiments, scene recognition for route and survey images revealed a cost for switching perspective from study to test. In addition, recognition performance was facilitated when the test view matched the observer's learned orientation but only for the same-perspective recognition test. Experiment 3 demonstrated orientation dependence in judgments of relative direction, with a strong emphasis on initial heading. Together, these results suggest that establishing a reference system for representing spatial information is dependent on specific characteristics of the learning situation.

Cues↗

PubMed1995

The effects of AMPA-induced lesions of the medial septum and vertical limb nucleus of the diagonal band of Broca on spatial delayed non-matching to sample and spatial learning in the water maze.

These experiments investigated in the rat the impact on spatial delayed non-matching to sample and on acquisition of the Morris water maze of (i) AMPA-induced lesions of the medial septal nucleus, which produced a marked reduction of hippocampal choline acetyltransferase activity and acetylcholine levels (measured using in vivo dialysis) together with lesser reductions in cholinergic markers in the cingulate cortex and (ii) similar AMPA-induced lesions of the vertical limb nucleus of the diagonal band of Broca (vDB), which produced more marked reductions in cholinergic markers in the cingulate cortex than in the hippocampus. Medial septal lesions produced a delay-dependent deficit in spatial working memory, while lesions of the vDB resulted in a delay-independent performance deficit. In addition, rats with vDB lesions adopted biased response strategies during the imposition of long delays. Neither lesion significantly affected the acquisition of a spatial reference memory task, the Morris water maze. The results are discussed in terms of cholinergic- and GABAergic-dependent functions of the hippocampal formation and cingulate cortex in spatial short-term and reference memory.

Acetylcholine↗

PubMed2005

Temporal factors in tactile spatial acuity: evidence for RA interference in fine spatial processing.

We investigated the extent to which subjects' ability to perceive the fine spatial structure of a stimulus depends on its temporal properties (namely the frequency at which it vibrates). Subjects were presented with static or vibrating gratings that varied in spatial period (1-8 mm) and vibratory frequency (5-80 Hz) and judged the orientation of the gratings, presented either parallel or perpendicular to the long axis of the finger. We found that the grating orientation threshold (GOT)-the spatial period at which subjects can reliably discriminate the orientation of the grating-increased as the vibratory frequency of the gratings increased. As the spatial modulation of SA1 and RA afferent fibers has been found to be independent of vibratory frequency, the frequency dependence of spatial acuity cannot be attributed to changes in the quality of the peripheral signal. Furthermore, we found GOTs to be relatively independent of stimulus amplitude, so the low spatial acuity at high flutter frequencies does not appear to be due to an inadequacy in the strength of the afferent response at those frequencies. We hypothesized that the RA signal, the strength of which increases with vibratory frequency, interfered with the spatially modulated signal conveyed by SA1 fibers. Consistent with this hypothesis, we found that adapting RA afferent fibers improved spatial acuity, as gauged by GOTs, at the high flutter frequencies.

Afferent Pathways↗

PubMed1995

Spatial working memory deficits in the relatives of schizophrenic patients.

BACKGROUND: Studies in nonhuman primates provide evidence that intact spatial working memory depends on the integrity of specific areas in the prefrontal cortex. Patients with schizophrenia have been shown to be impaired on spatial working memory tasks. Relatives of schizophrenic patients show a range of cognitive deficits in the absence of clinical symptoms (eg, thought disorder, eye tracking dysfunctions). We predicted that a significant proportion of relatives of schizophrenic patients would show deficits in working memory as measured by a delayed response task. METHODS: In experiment 1, we tested 18 schizophrenic patients, 15 first-degree relatives of schizophrenic patients, and 18 normal control subjects on an oculomotor delayed response task. In experiment 2, we assessed the performance of another group of 12 first-degree relatives of schizophrenic patients and 16 different normal control subjects on a visual-manual delayed response task. RESULTS: Relatives of schizophrenic patients showed significant deficits in working memory on both the oculomotor and visual-manual delayed response tasks. CONCLUSIONS: Some relatives of schizophrenic patients are impaired on tasks that tap spatial working memory and that implicate the prefrontal system. The delayed response paradigm may be useful in elucidating the multidimensionality of the schizophrenic phenotype.

Adult↗

PubMed2003

Learning deficits in forebrain-restricted brain-derived neurotrophic factor mutant mice.

Brain-derived neurotrophic factor (BDNF) participates in synaptic plasticity and the adaptive changes in the strength of communication between neurons thought to underlie aspects of behavioral adaptation. By selectively deleting BDNF from the forebrain of mice using the Cre site-specific DNA recombinase, we were able to study the requirements for BDNF in behaviors such as learning and anxiety. Early-onset forebrain-restricted BDNF mutant mice (Emx-BDNF(KO)) that develop in the absence of BDNF in the dorsal cortex, hippocampus, and parts of the ventral cortex and amygdala failed to learn the Morris Water Maze task, a hippocampal-dependent visuo-spatial learning task. Freezing during all phases of cued-contextual fear conditioning, a behavioral task designed to study hippocampal-dependent associative learning, was enhanced. These mice learned a brightness discrimination task well but were impaired in a more difficult pattern discrimination task. Emx-BDNF(KO) mice did not exhibit altered sensory processing and gating, as measured by the acoustic startle response or prepulse inhibition of the startle response. Although they were less active in an open-field arena, they did not show alterations in anxiety, as measured in the elevated-plus maze, black-white chamber or mirrored chamber tasks. Combined, these data indicate that although an absence of forebrain BDNF does not disrupt acoustic sensory processing or alter baseline anxiety, specific forms of learning are severely impaired.

Acoustic Stimulation↗