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PubMed2001

Host spatial heterogeneity and the spread of vector-borne infection.

We analyze how spatial heterogeneity in host density affects the advance of vector-borne disease. Infection requires vector infestation. The vector spreads only between hosts occupying the same neighborhood, and the number of hosts varies randomly among neighborhoods. Simulation of a spatially detailed model shows that increasing heterogeneity in host abundance reduces pathogen prevalence. Clumping of hosts can limit the advance of the vector, which inhibits the spread of infection indirectly. Clumping can also increase the chance that the pathogen and vector become physically separated during the initial phase of the epidemic process. The latter limitation on the pathogen's spread, in our simulations, is restricted to small interaction neighborhoods. A mean-field model, which does not maintain spatial correlations between sites, approximates simulation results when hosts are arrayed uniformly, but overestimates infection prevalence when hosts are aggregated. A pair approximation, which includes some of the simulation model's spatial correlations, better describes the vector infestation frequencies across host spatial dispersions.

Analysis of Variance↗
PubMed1991

Spatial-frequency-dependent changes in the human pattern electroretinogram after acute acetyl-L-carnitine administration.

Acetyl-L-carnitine (LAC) is a neuroactive compound that is thought to be involved in cholinergic transmission. The effects of acute intravenous LAC administration (30 mg/kg) on pattern-evoked electroretinograms (P-ERGs) were evaluated in nine healthy volunteers ranging in age between 21 and 27 years. Nine age-matched, normal subjects treated with a placebo served as controls. Steady-state (8 Hz) P-ERGs recorded in response to counterphased sinusoidal gratings of variable spatial frequency (0.6-4.8 cycles/degree) were obtained before and at 20, 50 and 80 min after LAC or placebo administration. The amplitude and phase of the Fourier-analysed P-ERG second harmonic were measured. As compared with placebo-treated controls, LAC-treated subjects showed a selective P-ERG amplitude increase (Mann-Whitney rank test: P less than 0.05), which was found 80 min posttreatment at a spatial frequency of 4.8 cycles/degree. For the same stimulus a significant (P less than 0.05) P-ERG phase shortening (at 50 min after drug administration) was also found. The spatial frequencies of other stimuli did not show a significant difference between the LAC- and placebo-treated groups. These results indicate that acute LAC administration induces a spatial-frequency-dependent enhancement of the human P-ERG. This is compatible with a cholinergic excitatory effect and suggests a therapeutic role for this compound in retinal dysfunctions with selective vulnerability to medium-high spatial frequencies.

Acetylcarnitine↗
PubMed1995

Modeling the electroencephalogram by means of spatial spline smoothing and temporal autoregression.

A spatial-temporal model for the description of electroencephalographic (EEG) data is introduced that combines smooth reconstruction in the spatial domain and autoregressive representation in the time domain. Its spatial aspect is formulated in a general framework that covers interpolation, smoothing, and regression. Contrary to the multivariate time series models used for EEG analysis up to date, the introduced model provides a smooth spatial reconstruction of the EEG cross-spectrum, keeping the condition of nonnegative definiteness. As an instance of practical importance, the case in which the spatial reconstruction is based on spherical splines is developed in detail. Illustrative examples are presented that show the flexibility of the model to describe both normal and abnormal EEG data.

Electroencephalography↗
PubMed1994

Function of GABAA inhibition in specifying spatial frequency and orientation selectivities in cat striate cortex.

Responses of simple and complex cells in cat striate cortex were studied with moving sine-wave gratings before and during application of the GABAA receptor antagonist bicuculline methiodide. Both simple and complex cells exhibited a broadening of their spatial frequency tuning functions under bicuculline. This was especially evident at spatial frequencies lower than the ones the cell was responding to before the drug administration. The effects cannot be explained by response saturation and could be reversed by cessation of the iontophoresis. The results indicate that the band-pass response characteristics of the spatial frequency response functions of striate cells derive largely from intracortical inhibition. The findings have implications also for the orientation selectivity of cortical cells. Since many geniculate cells are tuned for stimulus orientation at higher spatial frequencies, suppression of the low-spatial-frequency component would remove some of the orientation non-specific response in striate cortical cells and contribute to their orientation selectivity.

Animals↗
PubMed1984

Representation of spatial details in textured patterns by cells of the cat striate cortex.

The ability of single cells to represent the spatial details of textured stimuli was investigated. Two complementary aspects of cell response were considered, the ability to discriminate fine stimulus details and the property of integration over wider areas of a structure to encode differences in mean luminance. Responses of simple and complex cells were distinct in some respects. Spatial discrimination: Simple cells would encode orientation of line arrays as long as individual line elements could be spatially resolved. By contrast, complex cells were able to distinguish the orientation of texture areas even when the individual lines of the stimulus were not resolved in their response. Threshold sensitivity for texture orientation was of the same order in both cell classes despite differences in receptive field size. Spatial integration: Complex cells responded to texture luminance differences of much coarser patterns than did simple cells. These responses, however, were not biased for contour orientation unless finer patterns were used. Only with very fine textures did responses become indistinguishable from those to uniform stimuli for both simple and complex cells. For complex cells, there was a smooth transition from resolution to fusion of spatial details with increasing structural density. Simple cells were insensitive to both detailed and global properties of a stimulus pattern over a wide range of texture density. Implications for alternative measures of visual acuity of single cells are discussed.

Animals↗
PubMed1986

Effect of contrast on spatial frequency tuning of neurones in area 17 of cat's visual cortex.

Previous investigations have revealed that perceived spatial frequency of gratings rises as contrast is lowered. In order to account for this finding it has been postulated that the spatial frequency which produces the maximum response from cortical neurones decreases with contrast. We have examined this hypothesis by determining optimal spatial frequency at 3-5 different contrast levels for 37 neurones in the cat striate cortex. For the complete sample no systematic changes in optimal spatial frequency was observed. However, a shift in the predicted direction was found for cells tuned to high spatial frequencies.

Animals↗
PubMed1979

Behavioural studies of spatial vision in cats reared with convergent squint: is amblyopia due to arrest of development?

Visual acuity and contrast sensitivity were measured behaviourally in normal adult cats and cats reared with monocular convergent squint from 3, 6, 8, 12, and 24 weeks of age. The visual acuity of the squinting eye was significantly lower than that of the non-squinting eye in cats with squint from 3, 6, and 8 weeks of age. No significant difference in acuity between eyes was found in the 12- and 24-week squinting cats and in the controls. Contrast thresholds at all spatial frequencies tested (range 0.13--2.0 c/degrees) were higher in the squinting eye than in the non-squinting eye of cats with squint from 3 and 6 weeks of age, but differences were greater at the higher spatial frequencies. In the 8-week squinting cat, contrast thresholds were increased only at higher spatial frequencies. No significant differences in contrast sensitivity were found in the cat with squint from 24 weeks of age and in the controls. The degree of disturbance of spatial vision in squinting cats was most related to the age at onset of the squint, i.e., the earlier the onset, the more profound the amblyopia. The period of susceptibility extended from about 3 to 12 weeks of age. When compared with data on the development of visual acuity in kittens, the pattern of results from the present study suggests that convergent squint can arrest the development of spatial vision.

Age Factors↗
PubMed1995

A survey of spinal dorsal horn neurones encoding the spatial organization of withdrawal reflexes in the rat.

The withdrawal reflex pathways to hindlimb muscles have an elaborate spatial organization in the rat. In short, the distribution of sensitivity within the cutaneous receptive field of a single muscle has a spatial pattern that is a mirror image of the spatial pattern of the withdrawal of the skin surface ensuing on contraction in the respective muscle. In the present study, a search for neurones encoding the specific spatial input-output relationship of withdrawal reflexes to single muscles was made in the lumbosacral spinal cord in halothane/nitrous oxide-anaesthetized rats. The cutaneous receptive fields of 147 dorsal horn neurones in the L4-5 segments receiving a nociceptive input and a convergent input from A and C fibres from the hindpaw were studied. The spatial pattern of the response amplitude within the receptive fields of 118 neurones was quantitatively compared with those of withdrawal reflexes to single muscles. Response patterns exhibiting a high similarity to those of withdrawal reflexes to single muscles were found in 27 neurones located in the deep dorsal horn. Twenty-six of these belonged to class 2 (responding to tactile and nociceptive input) and one belonged to class 3 (responding only to nociceptive input). None of the neurones tested (n = 20) with reflex-like response patterns could be antidromically driven from the upper cervical cord, suggesting that they were spinal interneurones. With some overlap, putative interneurones of the withdrawal reflexes to the plantar flexors of the digits, the plantar flexors of the ankle, the pronators, the dorsiflexors of the ankle, and a flexor of the knee, were found in succession in a mediolateral direction.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed1994

The spatial patterns of beta/A4 deposit subtypes in Down's syndrome.

The spatial patterns of diffuse, primitive and classic beta/A4 deposits were studied in coronal sections of the hippocampus and adjacent gyri in 11 cases of Down's syndrome (DS) varying in age from 38 to 67 years. The objectives of the study were first, to compare the spatial patterns of beta/A4 deposits revealed in DS with those reported in cases of Alzheimer's disease (AD) and second, to study how the spatial patterns of beta/A4 deposits may develop in the tissue. The spatial patterns revealed in DS exhibited a number of similarities with those reported in AD: (1) the range and frequency of the different types of spatial pattern revealed were similar, (2) beta/A4 deposits occurred in clusters and in many cortical tissues, the clusters were distributed in a regular pattern parallel to the pia, (3) the clusters of diffuse and primitive beta/A4 deposits occurred in an alternating pattern along the cortex, and (4) the clusters of classic beta/A4 deposits were not correlated with the clusters of the diffuse and primitive deposits. Primitive deposits may develop from the diffuse deposits in regions of the cortex where extracellular paired helical filaments were formed. However, clusters of the classic beta/A4 deposits, which are formed in older cases, appear to develop independently of the diffuse and primitive deposits.

Adult↗
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↗
PubMed1994

The functional role of attention for spatial coding in the Simon effect.

Two experiments investigated relative spatial coding in the Simon effect. It was hypothesized that relative spatial coding is carried out with reference to the position of the focus of visual attention. The spatial code for an imperative stimulus presented exactly at the position of focal attention should be neutral on the horizontal plane, and therefore no Simon effect should be observed. However, when the imperative stimulus is presented to the left or to the right of the current position of focal attention, the spatial code should not be neutral, thus producing a Simon effect. In both experiments, focal attention was manipulated either by a peripherally presented onset precue (Experiment 1) or by a centrally presented symbolic precue (Experiment 2). Results showed that the Simon effect was substantially reduced in both experiments when a valid precue preceded the imperative stimulus just in time to conclude refocusing of attention to the position of the imperative stimulus before it was presented. However, conditions with neutral precues yielded a normally sized Simon effect. In both experiments, the Simon effect decreased as the SOA grew when the precue was valid. At least for the Simon effect, the results can be interpreted as evidence that relative spatial coding is functionally related to the position of the focus of attention.

Adult↗
PubMed1994

Hand-hemispace spatial compatibility, precueing, and stimulus-onset asynchrony.

The role of attention and the resolution of coding conflicts in hand-hemispace spatial-compatibility effects was examined in a precueing experiment in which visual and vibrotactile precues, with various stimulus-onset asynchronies (SOAs), were presented in blocked and random order. It was expected that precues at the shorter SOAs would fail to facilitate the shifting of attention, as they occur too close to the imperative stimulus to be informative. The task would therefore approximate one of choice reaction time (RT), resulting in a hand-hemispace spatial-compatibility effect. Conversely, the longer SOAs would provide the subject with sufficient time in which to shift attention fully, and would therefore result in a task more like that of simple reaction time (SRT). It was expected that the hand-hemispace spatial-compatibility effect would then be absent. As was expected, this effect was present at the shorter SOAs, and absent at the longer SOAs. In Experiments 2 and 3, provision of a visual precue further facilitated attentional deployment, as did blocking the presentation of various SOAs in Experiment 3. Vibrotactile and visual precues did not differ in their ability to direct attention, implying that these modalities orient attention and precue location in essentially similar ways. These findings are discussed within the context of the mechanisms though to underlie the time course of spatial compatibility and the dissipation of a fading trace of interfering spatial codes.

Adult↗
PubMed1989

Hemicholinium-3 impairs spatial learning and the deficit is reversed by cholinomimetics.

The effects of hemicholinium-3 (HC-3) on spatial discrimination learning were studied. Rats were equipped with indwelling cannulae in the right lateral ventricle and, following recovery, were trained on a two platform spatial discrimination task in a water maze. In this task a visible escape platform remains in a fixed position in the pool during a single training session, whilst the location of an identical "float" (which affords no escape) is randomly varied. For each session the location of the fixed escape platform was changed and the rats were retrained to criterion following pretreatment either with artificial cerebrospinal fluid (CSF) or HC-3 (2.5, 5.0 micrograms/rat/ICV) 1 h before training. Each rat received every treatment according to a latin square design. The results showed that spatial learning was dose dependently impaired by HC-3, choice accuracy being reduced to chance levels by the higher dose. There was no evidence of motoric difficulty, as choice latencies were not significantly increased. Experiments were then conducted to test for reversal of the deficit using a range of psychotropic drugs. Rats were treated with CSF or HC-3 (5 micrograms/rat ICV) 60 min prior to testing and test drugs were injected 15 min before testing. Some doses of physostigmine (46-460 micrograms/kg/SC) and tetrahydroaminoacridine (THA) (2.2-10 mg/kg/SC) reversed the spatial learning deficit. The muscarinic agonists arecoline (0.046-1 mg/kg/SC), aceclidine (1-10 mg/kg/SC), oxotremorine (30-100 micrograms/kg/SC) and RS-86 (0.46, 1.0 microgram/kg/SC) were also effective. Pilocarpine (0.22-2.2 mg/kg/SC) showed marginal activity and isoarecoline (4.6-10 mg/kg/SC) was inactive. Nicotine (0.32, 1, 3.2 mg/kg/SC) and piracetam (10, 30, 100 mg/kg IP) were also inactive. The alpha 2 agonist, clonidine (46, 100 micrograms/kg SC) and the antagonist idazoxan (32, 100 micrograms/kg SC) were also inactive. Learning deficits were not reversed by haloperidol (20, 60 micrograms/kg), amphetamine (0.1, 0.46 mg/kg), the selective 5-HT1A agonist 8-OH-DPAT (30, 100 micrograms/kg) or by the benzodiazapine antagonist ZK-93426 (1, 3.2, 10 mg/kg). The results show that forebrain Ach depletion by HC-3 impairs spatial discrimination learning and these deficits are reversed by cholinesterase inhibitors and some muscarinic receptor agonists. Some degree of pharmacological selectivity is indicated by the failure of a range of other drugs to reverse the impairments.

8-Hydroxy-2-(di-n-propylamino)tetralin↗
PubMed1989

Spatial and spatiotemporal contrast sensitivity of normal and glaucoma eyes.

The spatial contrast sensitivity (CS) to static patterns was tested in the central retina of 156 normal subjects. It showed a decrease above 50 years of age at all spatial frequencies tested which was slightly more pronounced in females than in males. The spatial CS was also studied in 32 glaucoma eyes: Small reductions were found only in the group below 50 but not in eyes of patients above 50. The spatiotemporal CS to phase-reversing patterns was tested in four retinal quadrants of 99 normal subjects. It showed no age dependence in males whereas in females it decreased significantly beyond 50 years at all spatial frequencies tested. The spatiotemporal CS was studied also in 21 glaucoma eyes: Strong losses were again noted only in patients below 50. Spatiotemporal CS losses and perimetric losses were also compared in the four quadrants: For both measures the severest losses were found in the lower nasal and the mildest in the upper temporal quadrant. The spatiotemporal CS test of the peripheral retina seems to be a more powerful tool in glaucoma research than the spatial CS test of the central retina; however, effects of age and gender have to be considered.

Adult↗
PubMed2003

Single motor unit analysis from spatially filtered surface electromyogram signals. Part 2: conduction velocity estimation.

The aim of the study was to compare experimentally conduction velocity (CV) estimates obtained with different estimation methods based on surface electromyogram (EMG) signals detected using five spatial filters. The filters investigated were the longitudinal single and double differential, transverse single and double differential, and normal double differential. The same surface EMG signals detected as described in Part 1 were used in this work. CV was estimated with four commonly used delay estimation techniques, i.e. from the distance between the peak values of two waveforms (with and without polynomial interpolation around the peak), and by the maximum likelihood estimate (MLE) based on two or more surface EMG channels. The average standard deviation of CV estimation (for all the MUs and the two muscles together) was 0.61 m s(-1) and 0.79 m s(-1) for the peak method, with and without interpolation, respectively, and 0.50 m s(-1) and 0.31 m s(-1) for the MLE method, from two and more surface EMG channels, respectively. Moreover, the mean of CV estimates varied by as much as 1 m s(-1) depending on the spatial filter used and the method adopted for CV estimation. Considering the dependence on the spatial filter only, the average (over all estimation methods) CV estimates obtained with the five spatial filters were 4.32 m s(-1) (normal double differential), 4.23 m s(-1) (longitudinal double differential), 4.61 m s(-1) (transverse double differential), 4.64 m s(-1) (transverse single differential) and 4.03 m s(-1) (longitudinal single differential). It was concluded that the comparison of single MU CV values obtained in different studies is critical if different spatial filters and processing techniques are used for their estimation. Higher estimates of CV were attributed to a smaller reduction in non-travelling signal components and thus were assumed to be positively biased.

Action Potentials↗
PubMed2004

Spatial filters based on independent component analysis for magnetic noise reduction in the magnetocardiogram.

A spatial filter design method to reduce magnetic noise in the magnetocardiogram (MCG) is introduced. Based on the facts that external magnetic noise appearing on multichannel MCG sensors is independent of the cardiac signals and that there is strong spatial correlation among the channels, the independent component analysis (ICA) method was applied to extract the noise components from the measured MCG signals. After extraction of the noise components in a given time period using ICA, a spatial filter was made to reduce the noise components in subsequently acquired MCG signals. In experimental studies of nine healthy volunteers, the spatial filters improved the signal-to-noise ratio of the MCG signals by about 500% on average. This spatial filtering method can be used for measurements of MCG signals in a magnetically noisy environment.

Artifacts↗
PubMed1991

Methodological error and spatial variability of organ blood flow measurements using radiolabeled microspheres.

The quantitative analysis of the spatial variability of organ blood flow by means of radiolabeled microspheres (MS) requires that the methodological variability ("error") of the technique (RDmeth.) is known in each individual organ. Therefore, RDmeth. was quantified (eight to nine nuclides) in 6941 tissue samples from 13 organs of three anesthetized dogs, and the relative importance of errors originating from both the stochastic nature of MS distribution (RDtheo.) and the process of quantitation of MS radioactivity (RDcounting) was assessed under varying conditions (high/low specific MS activity (SAMS); inaccurate separation of gamma spectra; large sample size). At "minimized" methodological error (experiment 2), RDmeth. of samples trapping approximately 375 MS/nuclide was 5.8% and only slightly exceeded RDtheo. (5%). RDmeth. varied in the range 2.7-7.8% in individual organs and contributed little (3.5%) to the organs' observed spatial variability of flow. In contrast, RDmeth.--due to increased RDcounting--considerably exceeded RDtheo. when SAMS was low (experiment 3), overlap of two nuclides' main photopeaks was critical (experiment 1), or counting geometry was inappropriate (pulmonary tissue samples). At the same time, the contribution of RDmeth. to spatial flow variability rose to 7.9% (experiment 3), 26.9% (experiment 1), and 15-23% (lungs). Completely artifactual measurements, as indicated by an extremely high RDmeth. of sample flow, were rarely observed (less than 0.1%). In general, our data suggest that blood flow can be measured reproducibly and with low methodological error using up to 8 nuclides, RDmeth. does not essentially contribute to the observed spatial variability of organ blood flow, and, hence, organ flow variability may be accurately quantified using the MS technique. However, if sources of error as indicated above are present, the practice of using RDtheo. as a measure of RDmeth. (thereby neglecting RDcounting) may notably underestimate true MS error and result in an overestimation of spatial heterogeneity of organ blood flow. RDmeth., therefore, should be quantified separately in each region of interest prior to the onset of a new study.

Animals↗
PubMed1983

A theory of measurement error and its implications for spatial and temporal gradient sensing during chemotaxis. II. The effects of non-equilibrated ligand binding.

Cells generally chemotax along a direction in which their receptor occupancy gradient--whether spatial or temporal--is maximum. Occupancy differentials are, however, often so small as to be masked by thermal noise; i.e., by fluctuations inherent in the stochastic nature of ligand binding. Such fluctuations therefore impose a fundamental limit on the sensitivity of a cell's ability to detect a chemoattractant gradient. In order to pursue the implications of this limit, fluctuation theories have been developed. The theories assume that the signal is some function of the receptor occupancy gradient, allow an estimate of the standard deviation about the mean signal, and permit an evaluation of, among other things, the extent to which a receptor defect can impair an effective response. Previous theories have assumed an equilibrated ligand-receptor interaction. In this paper we introduce a generalized definition of a signal caused by a receptor occupancy gradient that allows us to develop a non-equilibrium theory of thermal noise. We show that previous formulations are a special case of the current development. More specifically, we find the following. Swimming cells subject to Brownian tumbling must generally average their signals over a very long time period to achieve a signal-to-noise ratio less than or equal to 1. Spatial gradient detection is possible with ligand-receptor equilibrium constants less than 10(3)M-1, but since such ligands are rare, theory predicts that tumbling cells will generally not detect gradients by measuring spatial occupancy differentials. These conclusions hold irrespective of whether chemical equilibrium is achieved. For crawling cells not subject to Brownian tumbling, a range of affinities exists in which spatial or temporal gradient detection is possible. In general a spatial mechanism is more efficient for low affinity ligands (dissociation times less than 0.3 s), whereas a temporal mechanism is more efficient for higher K. In this case the detection of gradients in slowly dissociating ligand will be facilitated if signal processing begins prior to chemical equilibration. An important new parameter is indicated by the theory. The definitions of a temporal gradient signal is based on estimating and comparing average occupancy over two time intervals displaced by a time t1. The theory predicts an optimal t1, of order milliseconds, that leads to the shortest minimum averaging time. For t1 values at and longer than the optimum, and for all averaging times exceeding some minimum, the cell will detect a temporal signal.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗