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PubMed2005

Frequency and timing of severe hypoglycemia affects spatial memory in children with type 1 diabetes.

OBJECTIVE: Repeated severe hypoglycemia has been reported to reduce long-term spatial memory in children with type 1 diabetes. Early exposure to hypoglycemia may be more damaging to cognitive function than later exposure. Our goal was to determine whether the age at which severe hypoglycemia occurs modulates the impact of severe hypoglycemia frequency on long-term spatial memory. RESEARCH DESIGN AND METHODS: We combined data from three independent studies to obtain a sample of children aged 6-18 years with type 1 diabetes (n = 103) and nondiabetic control subjects (n = 60). Each study evaluated previous severe hypoglycemia and tested short (5 s)- and long (60 s)-delay spatial memory with the spatial delayed response task. Type 1 diabetic participants were categorized as having zero, one to two, or three or more severe hypoglycemic episodes and as having their first severe hypoglycemic episode before or after 5 years of age. Information on chronic hyperglycemia (HbA1c values) was also collected. RESULTS: We found that repeated severe hypoglycemia (more than three episodes) reduced long-delay spatial delayed response performance, particularly when severe hypoglycemic episodes began before the age of 5 years. Age of type 1 diabetes onset and estimates of chronic hyperglycemia did not influence performance. CONCLUSIONS: High frequency of and early exposure to severe hypoglycemia during development negatively affects spatial long-term memory performance.

Adolescent↗
PubMed1993

Extraversion-introversion and spatial intelligence.

The purpose of this study was to assess whether extraversion-introversion is related to spatial intelligence. First-year psychology students (58 men, 108 women) in an open-admission community college responded to a battery of black and white and color spatial ability tests, and the Eysenck Personality Inventory. As hypothesized, a small but significant relationship was found between scores on extraversion and on the SEK Test (colored spatial test). Gender differences in performance on the spatial tests favored males. Scores on three of the Spatial Dimensionality Tests correlated significantly with those on the SEK Test. Recommendations include investigating the effect of a variety of spatial problems in combination with other personality variables.

Adolescent↗
PubMed1994

Selective adaptation to low spatial frequencies does not decrease the Mueller-Lyer illusion.

The idea that low spatial-frequency information in the Mueller-Lyer figure accounts for a major part of the illusion was tested in a series of five studies. In Study 1, subjects were selectively adapted to high or low square-wave spatial-frequency gratings with no difference in the magnitude of illusion they experienced. Similarly, adaptation to sinusoidal grating patterns with either high or low spatial frequency had no effect on the magnitude of illusion experienced (Studies 2 to 5). The failure of adaptation to low spatial-frequency gratings to affect the magnitude of illusion experienced indicates either that the illusion cannot be accounted for by the low spatial-frequency information or that adaptation of the visual system by grating patterns cannot be used to explore any effects of the low spatial frequencies in the figure.

Adult↗
PubMed2000

Block design as a measure of everyday spatial ability: a study of ecological validity.

This study investigated the effectiveness of the WAIS-R Block Design subtest to predict everyday spatial ability for 65 university undergraduates (15 men, 50 women) who were administered Block Design, the Standardized Road Map Test of Direction Sense, and the Everyday Spatial Activities Test. In addition, the verbally loaded National Adult Reading Test was administered to assess whether the more visuospatial Block Design subtest was a better predictor of spatial ability. Moderate support was found. When age and sex were accounted for, Block Design accounted for 36% of the variance in performance (r = -.62) on the Road Map Test and 19% of the variance on the performance of the Everyday Spatial Activities Test (r = .42). In contrast, the scores on the National Adult Reading Test did not predict performance on the Road Map Test or Everyday Spatial Abilities Test. This suggests that, with appropriate caution, Block Design could be used as a measure of everyday spatial abilities.

Adolescent↗
PubMed1997

Yoga breathing through a particular nostril increases spatial memory scores without lateralized effects.

Uninostril breathing facilitates the performance on spatial and verbal cognitive tasks, said to be right and left brain functions, respectively. Since hemispheric memory functions are also known to be lateralized, the present study assessed the effects of uninostril breathing on the performance in verbal and spatial memory tests. School children (N = 108 whose ages ranged from 10 to 17 years) were randomly assigned to four groups. Each group practiced a specific yoga breathing technique: (i) right nostril breathing, (ii) left nostril breathing, (iii) alternate nostril breathing, or (iv) breath awareness without manipulation of nostrils. These techniques were practiced for 10 days. Verbal and spatial memory was assessed initially and after 10 days. An age-matched control group of 27 were similarly assessed. All 4 trained groups showed a significant increase in spatial test scores at retest, but the control group showed no change. Average increase in spatial memory scores for the trained groups was 84%. It appears yoga breathing increases spatial rather than verbal scores, without a lateralized effect.

Adolescent↗
PubMed2006

Spatial and temporal patterns of herd somatic cell score in france.

Spatial and temporal patterns of annual milk somatic cell score (ASCS) were explored in French dairy herds between 1996 and 2000 to detect regional singularities for risk of mastitis. A new cluster detection method was used, which was adapted to continuous variables and which allowed ASCS variation factors to be taken into account. The statistical unit was the herd-year. A linear regression model for each year allowed adjustment for breed, mean parity, number of calvings for each season, herd size, and farm altitude. Cluster detection was performed on raw data and on residuals of the model through a method based on the Hellinger distance between spatial distributions. The Hellinger distance between farm distributions was computed at different levels of ASCS (or residuals). Temporal ASCS patterns were explored using a computation of correlations and comparisons between spatial structures of the different years. The general ASCS trend over the study period was a decrease. The global Hellinger distance, which was higher than what could have been randomly expected for each of the 5 yr, indicated a significant spatial cluster formation. Cluster mapping over the 5 yr identified several areas, which sometimes differed between detection using raw data and that using ASCS residuals. Temporal correlations between ASCS residuals for each year were positive and decreasing, and 1996 and 2000 appeared spatially different from the other years. The more affected areas were regions that were not specialized in dairy production. During the study period, 2 progressive movements were detected, corresponding to a disappearance of clusters in the northwest and an increase of clusters in the southwest. Cluster detection could aid in the identification of new risk factors that are relevant at different spatial scales, and could help local organizations to supervise the risk of mastitis, and improve udder health management.

Animals↗
PubMed2006

Seeing ahead: experience and language in spatial perspective.

Spatial perspective can be directed by various reference frames, as well as by the direction of motion. In the present study, we explored how ambiguity in spatial tasks can be resolved. Participants were presented with virtual reality environments in order to stimulate a spatialreference frame based on motion. They interacted with an ego-moving spatial system in Experiment 1 and an object-moving spatial system in Experiment 2. While interacting with the virtual environment, the participants were presented with either a question representing a motion system different from that of the virtual environment or a nonspatial question relating to physical features of the virtual environment. They then performed the target task assign the label front in an ambiguous spatial task. The findings indicate that the disambiguation of spatial terms can be influenced by embodied experiences, as represented by the virtual environment, as well as by linguistic context.

Adolescent↗
PubMed2005

Spatial context learning in visual search and change detection.

Humans conduct visual search more efficiently when the same display is presented for a second time, showing learning of repeated spatial contexts. In this study, we investigate spatial context learning in two tasks: visual search and change detection. In both tasks, we ask whether subjects learn to associate the target with the entire spatial layout of a repeated display (configural learning) or with individual distractor locations (nonconfigural learning). We show that nonconfigural learning results from visual search tasks, but not from change detection tasks. Furthermore, a spatial layout acquired in visual search tasks does not enhance change detection on the same display, whereas a spatial layout acquired in change detection tasks moderately enhances visual search. We suggest that although spatial context learning occurs in multiple tasks, the content of learning is, in part, task specific.

Adult↗
PubMed2002

Made you blink! Contingent attentional capture produces a spatial blink.

Previous studies have shown that the capture of attention by an irrelevant stimulus can be eliminated by fore knowledge of the spatial location of the relevant target stimulus. To explore whether spatial certainty is sufficient to eliminate capture, four experiments are reported in which the spatial location of the target is certain but the temporal position is uncertain. Subjects viewed a central rapid serial visual presentation stream in which a target letter was defined by a particular color (e.g., red). On critical trials, irrelevant color singletons appeared in the periphery. In Experiments 1 and 2, peripheral singletons produced a decrement in central target identification that was contingent on the match between the singleton color and the target color. Experiments 3 and 4 provided evidence that this decrement reflected a shift of spatial attention to the location of the distractor. The results suggest that spatial certainty is not sufficient to eliminate attentional capture and that attentional capture can result in a spatial "blink" that is conditional on top-down attentional control settings.

Attention↗
PubMed2002

No evidence for overshadowing or facilitation of spatial pattern learning by visual cues.

Two experiments were conducted to examine the effects of redundant and relevant visual cues on spatial pattern learning. Rats searched for hidden food items on the tops of poles that formed a square (Experiment 1) or a checkerboard (Experiment 2) pattern. The experimental groups were trained with visual cues that specified the locations of the baited poles. All groups were tested without visual cues so that any overshadowing or facilitation of spatial pattern learning by visual cues could be detected. Spatial choices were controlled by the spatial pattern and by the visual cues in both experiments. However, there was no evidence of overshadowing or facilitation of spatial pattern learning by visual cues in either experiment. The results are consistent with the idea that the representation of the spatial pattern that guides choices is not controlled by the same learning processes as those that produce associations between visual cues and food locations.

Animals↗
PubMed2002

The time course of spatial memory distortions.

Four experiments investigated the memory distortions for the location of a dot in relation to two horizontally aligned landmarks. In Experiment 1, participants reproduced from memory a dot location with respect to the two landmarks. Their performance showed a systematic pattern of distortion that was consistent across individual participants. The three subsequent experiments investigated the time course of spatial memory distortions. Using a visual discrimination task, we were able to map the emergence of spatial distortions within the first 800 msec of the retention interval. After retention intervals as brief as 50 msec, a distortion was already present. In all but one experiment, the distortion increased with longer retention intervals. This early onset of spatial memory distortions might reflect the almost immediate decay of detailed spatial information and the early influence of an enduring spatial memory representation, which encodes spatial information in terms of the perceived structure of space.

Adult↗
PubMed2003

Simultaneous spatial updating in nested environments.

When one moves, the spatial relationship between oneself and the entire world changes. Spatial updating refers to the cognitive process that computes these relationships as one moves. In two experiments, we tested whether spatial updating occurs automatically for multiple environments simultaneously. Participants turned relative to either a room or the surrounding campus buildings and then pointed to targets in both the environment in which they turned (updated environment) and the other environment (nonupdated environment). The participants automatically updated the room targets when they moved relative to the campus, but they did not update the campus targets when they moved relative to the room. Thus, automatic spatial updating depends on the nature of the environment. Implications for theories of spatial learning and the structure of human spatial representations are discussed.

Attention↗
PubMed1990

Visual persistence of spatially filtered images.

Periodic stimuli such as sine-wave gratings and checkerboard patterns have been used in many studies of visual perception. It is well known that with such stimuli, visual persistence increases as spatial frequency increases and as contrast decreases. It is not clear, however, that similar relationships obtain for aperiodic stimuli such as natural images. Digitized images of objects (a face and a vase) were submitted to two-dimensional Fourier analysis. Four pairs of spatial frequency band-limited images were created for each image. Each pair consisted of a normal (NP) and a scrambled (SP) phase version, with the magnitude spectrum and space-averaged luminance the same within each pair. Filter bandwidths were one octave wide. Threshold persistence was measured for each spatially filtered image. Visual persistence for SP images increased significantly as spatial frequency increased, whereas no significant differences were found for NP images. This suggests that the temporal processing of complex, aperiodic visual images is influenced by the spatial frequency and contrast of local features within the image and cannot be predicted by space-averaged estimates of contrast and spatial frequency.

Adult↗
PubMed1989

Spatial S-R compatibility with orthogonal stimulus-response relationship.

Spatial stimulus-response (S-R) compatibility with unimanual two-finger choice reactions was investigated under conditions in which the spatial orientation of response keys was either parallel to or perpendicular to the orientation of the stimuli. Subjects responded to green or red lights in the left or right visual field (irrelevant stimulus location). The response keys were oriented horizontally on the left or right side of the body midline parallel to the stimuli, and were pressed with the palms facing down (Condition A), or were oriented orthogonally to the stimuli in the midsaggital plane, either horizontally and pressed with palms facing down (B) or facing up (C), or vertically and pressed with palms facing the body (D). The results for Condition A demonstrate the usual spatial S-R compatibility effect between field of stimulation and spatial position of responding finger. For Conditions B and D, a strong reaction time advantage still obtained for those stimulus-finger pairings that are compatible under Condition A. Condition C revealed an RT advantage for the opposite pairings. This shift of the compatibility effect from Condition B to Condition C indicates that the left/right distinction of fingers does not follow a simple, fixed spatio-anatomical mapping rule. The results are discussed within the framework of a hierarchical model of spatial S-R compatibility, with spatial coding and spatio-anatomical mapping as factors.

Adult↗
PubMed1989

Spatial frequencies and the cerebral hemispheres: contrast sensitivity, visible persistence, and letter classification.

The hypothesis that the two cerebral hemispheres are specialized for processing different visual spatial frequencies was investigated in three experiments. No differences between the left and right visual fields were found for: (1) contrast-sensitivity functions measured binocularly with vertical gratings ranging from 0.5 to 12 cycles per degree (cpd); (2) visible persistence durations for 1- and 10-cpd gratings measured with a stimulus alternation method; and (3) accuracy (d') and reaction times to correctly identify digitally filtered letters as targets (L or H) or nontargets (T or F). One significant difference, however, was found: In Experiment 3, a higher decision criterion (beta) was used when filtered letters were identified in the right visual field than when they were identified in the left. The letters were filtered with annular, 1-octave band-pass filters with center spatial frequencies of 1, 2, 4, 8, and 16 cpd. Combining four center frequencies with three letter sizes (0.5 degrees, 1 degree, and 2 degrees high) made some stimuli equivalent in distal spatial frequency (cycles per object) and some equivalent in proximal spatial frequency (cycles per degree). The effective stimulus in the third experiment seemed to be proximal spatial frequency (cycles per degree) not distal (cycles per object). We conclude that each cerebral hemisphere processes visual spatial frequency information with equal accuracy but that different decision rules are used.

Adult↗
PubMed1997

The effect of spatial frequency on global precedence and hemispheric differences.

There are many conditions in which identification proceeds faster for the global form of a hierarchical pattern than for it's local parts. Since the global form usually contains more lower spatial frequencies than do the local forms, it has frequently been suggested that the higher transmission rate of low spatial frequencies is responsible for the global advantage. There are also functional hemispheric differences. While the right hemisphere is better at processing global information, the left hemisphere has an advantage with respect to local information. In accordance with the spatial-frequency hypothesis, it has been speculated that this difference is due to a differential capacity of the hemispheres for processing low and high spatial frequencies. To test whether low spatial frequencies were responsible for the global advantage and/or for the observed hemispheric differences, two experiments were carried out with unfiltered and highpass-filtered compound-letter stimuli presented at the left, right, or center visual field. The first experiment, in which the target level was randomized in each trial block, revealed that low spatial frequencies were not necessary for either global advantage or for hemispheric differences. Highpass filtering merely increased the response times. In the second experiment, the target level was held constant in each block. This generally increased the speed of responding and produced interactions between filtering and global-local processing. It was concluded that both sensory and attentional or control mechanisms were responsible for global precedence and that the hemispheres differed with respect to the latter.

Adult↗
PubMed1999

Anatomic validation of spatial normalization methods for PET.

UNLABELLED: Spatial normalization methods, which are indispensable for intersubject analysis in current PET studies, have been improved in many aspects. These methods have not necessarily been evaluated as anatomic normalization methods because PET images are functional images. However, in view of the close relation between brain function and morphology, it is very intriguing how precisely normalized brains coincide with each other. In this report, the anatomic precision of spatial normalization is validated with three different methods. METHODS: Four PET centers in Japan participated in this study. In each center, six normal subjects were recruited for both H2(15)O-PET and high-resolution MRI studies. Variations in the location of the anterior commissure (AC) and size and contours of the brain and the courses of major sulci were measured in spatially normalized MR images for each method. Spatial normalization was performed as follows. (a) Linear: The AC-posterior commissure and midsagittal plane were identified on MRI and the size of the brain was adjusted to the Talairach space in each axis using linear parameters. (b) Human brain atlas (HBA): Atlas structures were manually adjusted to MRI to determine linear and nonlinear transformation parameters and then MRI was transformed with the inverse of these parameters. (c) Statistical parametric mapping (SPM) 95: PET images were transformed into the template PET image with linear and nonlinear parameters in a least-squares manner. Then, coregistered MR images were transformed with the same parameters used for the PET transformation. RESULTS: The AC was well registered in all methods. The size of the brain normalized with SPM95 varied to a greater extent than with other approaches. Larger variance in contours was observed with the linear method. Only SPM95 showed significant superiority to the linear method when the courses of major sulci were compared. CONCLUSION: The results of this study indicate that SPM95 is as effective a spatial normalization as HBA, although it does not use anatomic images. Large variance in structures other than the AC and size of the brain in the linear method suggests the necessity of nonlinear transformations for effective spatial normalization. Operator dependency of HBA also must be considered.

Brain↗
PubMed1976

Attenuation of vibrotactile spatial summation.

Masked and quiet thresholds at several frequencies of vibratory stimuli were measured as a function of contactor area. The test site was the left index finger; the masking site was the left little finger. The quiet threshold data were consistent with previous investigations: Low-frequency stimuli showed no spatial summation, whereas high-frequency stimuli did. In the presence of a masker, spatial summation was reduced or eliminated for high-frequency stimuli, i.e., the masked threshold was, under some conditions, independent of contactor area. Low-frequency stimuli continued to show no spatial summation in the presence of a masker. The attenuation of spatial summation appears to be a direct function of the intensity of the masking stimulus. Additional measurements with the left thenar eminence as the test site showed that spatial summation could be attenuated by a masker placed on a contralateral body site. The implications of the results for quantifying the effectiveness of a masking stimulus, for the duplex mechanoreceptor hypothesis, and for the nature of spatial summation on the skin are discussed.

Adult↗