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At least 181 records · Page 10Linked to original sources
PubMed2006

A sensitive method for measuring spatial orientation in bone structures.

OBJECTIVES: This article introduces the newly developed line frequency deviation (LFD) method for measuring the orientation of the trabecular structure and shows that it is more sensitive than the mean intercept length (MIL) method that is commonly used. METHODS: The LFD method, which has been developed to measure the orientation of bone on two-dimensional X-ray images, was expanded to handle three-dimensional shapes. For the purpose of comparison, both the LFD and the MIL methods were applied to micro CT scans of 24 trabecular bone samples as well as to 24 simple synthetic samples. LFD and MIL values were calculated in various directions and collected in polar plots. Next, the anisotropy was quantified by calculating the coefficient of variation as well as by fitting ellipsoids through the plots. RESULTS: The MIL method yielded smooth rather spherical ellipsoidal polar plots with almost no sensitivity for changes in structure. The LFD method yielded more slender polar plots and more sensitivity for geometrical changes. The LFD method yielded significantly more anistropy and larger variation in anisotropy. CONCLUSIONS: The LFD method is a more sensitive descriptor of spatial orientation of bone structures than the MIL method.

Anisotropy↗
PubMed2000

Proprioceptive population coding of two-dimensional limb movements in humans: I. Muscle spindle feedback during spatially oriented movements.

The proprioceptive coding of multidirectional ankle joint movements was investigated, focusing in particular on the question as to how accurately the direction of a movement is encoded when all the proprioceptive information from all the muscles involved in the actual movement is taken into account. During ankle movements imposed on human subjects, the activity of 30 muscle spindle afferents originating in the extensor digitorum longus, tibialis anterior, extensor hallucis longus and peroneus lateralis muscles was recorded from the lateral peroneal nerve using the microneurographic technique. In the first part of the study, it was proposed to investigate whether muscle spindle afferents have a preferred direction, as previously found to occur in the case of cortical cells, and to analyze the neural coding of the movement trajectories using a "population vector model." This model is based on the idea that neuronal coding can be analyzed in terms of a series of vectors, each based on specific movement parameters. In the present case, each vector gives the mean contribution of a population of muscle spindle afferents within one directionally tuned muscle. A given population vector points in the "preferred sensory direction" of the muscle to which it corresponds, and its length is the mean frequency of all the afferents within that muscle. Our working hypothesis was that the sum of these weighted vectors points in the same direction as the ongoing movement. The results show that each muscle spindle afferent, and likewise each muscle, has a specific preferred sensory direction, as well as a preferred sensory sector within which it is capable of sending sensory information to the central nervous system. Interestingly, the results also demonstrate that the preferred directions are the same as the directions of vibration-induced illusions. In addition, the results show that the neuronal population vector model describes the multipopulation proprioceptive coding of spatially oriented 2D limb movements, even at the peripheral sensory level, based on the sum vectors calculated from all the muscles involved in the movement. In an accompanying paper, the coding of more complex 2D movements such as those involved in drawing rectilinear and curvilinear geometrical shapes was investigated.

Adult↗
PubMed2002

The nodulus and uvula: source of cerebellar control of spatial orientation of the angular vestibulo-ocular reflex.

The nodulus and rostral-ventral uvula of the vestibulo-cerebellum play a critical role in orienting eye velocity of the slow component of the angular vestibulo-ocular reflex (aVOR) to gravito-inertial acceleration (GIA). This is done by altering the time constants of "velocity storage" in the vestibular system and by generating "cross-coupled" eye velocities that shift the eye velocity vector from along the body yaw axis to the yaw axis in a spatial frame. In this report, we show that eye velocity generated through the aVOR by constant velocity centrifugation in the monkey orients to the GIA in space, regardless of the position of the head with respect to the axis of rotation. We also show that, after removal of the nodulus and rostral-ventral uvula, the spatial orientation of eye velocity to the GIA is lost and that eye velocity is then purely driven by the semicircular canals in a body frame of reference. These findings are further confirmation that these regions of the vestibulo-cerebellum control spatial orientation of the aVOR.

Animals↗
PubMed2005

Two electrophysiological stages of spatial orienting towards fearful faces: early temporo-parietal activation preceding gain control in extrastriate visual cortex.

Visuo-spatial attention tends to be prioritized towards emotionally negative stimuli such as fearful faces, as opposed to neutral or positive stimuli. Using a covert orienting task, we previously showed that a lateral occipital P1 component, with extrastriate neural sources, was selectively enhanced to lateralized visual targets replacing a fearful face (fear-valid trial) than the same targets replacing a neutral face (fear-invalid trial), providing evidence for exogenous spatial orienting of attention towards threat cues. Here, we describe a new analysis of these data, using topographic evoked potentials mapping methods combined with a distributed source localization technique. We show that an early field topography (40-80 ms post-target onset) with a centro-parietal negativity and a left posterior parietal source distinguished fear-valid from fear-invalid trials, whereas a distinct activity with anterior cingulate sources was selectively evoked during fear-invalid trials. At the same latency, or later, no difference in field topography was found for valid compared to invalid trials with happy faces. The early parietal map preceded a modulation in amplitude of the field strength (approximately 130 ms), corresponding to the enhanced lateral occipital P1 during valid trials in the fear condition. Furthermore, this early topography at 40-80 ms was positively correlated with the subsequent amplitude modulation of P1 at 130-160 ms in the fear condition, suggesting a possible functional coupling between these two successive events. These data have important implications for models of spatial attention and interactions with emotion. They suggest two successive stages of neural activity during exogenous orienting of attention towards visual targets following fearful faces, including an early posterior parietal negativity, followed by gain control mechanisms enhancing visual responses in extrastriate occipital cortex.

Adult↗
PubMedDate not supplied

Disturbed visuo-spatial orientation in the early stage of Alzheimer's dementia.

A pilot study was conducted to assess previously unrecognized visuo-spatial disturbances in 45 Alzheimer's demented (AD) patients and 59 control persons all over the age of 65 years, living in the community. The results of the Clock Drawing Test (CDT) revealed high frequency (78%) of deficient performative visuo-spatial skills of mild and moderate demented AD patients. The severity of dementia was found to be a good predictor of the deficit in visuoconstructive performance. The most frequent drawing mistakes were the misplacement of numbers and clock hands, which may relate to dysfunctions of the right inferior parietal cortex. The right-left orientation (RLO) for the own body was not deteriorated in AD patients. However, significantly lower scores for RLO in the mental rotation subtest were found in mild and moderate AD groups. There were large inter-individual differences in the test scores of both demented groups. Thirty-one percent and 49% of the AD patients scored 0 points or within the normal range (more than 4 points), respectively, indicating a pseudofocal onset pattern of the dementia. The results of the CDT and Right-Left Orientation Test (RLOT) with Mental rotation showed significant positive correlation with other cognitive functions of Mini Mental State Exam, such as attention-calculation, recall and writing, and indicate that the visuo-spatial orientation (VSO) is a composite of different cognitive skills. The CDT and RLOT appears to be a useful tool for screening the elderly for disturbed VSO.

Journal Article↗
PubMed1998

Development of spatial memory and spatial orientation in preschoolers and primary school children.

The present study addresses the question of what kind of information children use when orientating in new environments, if given proximal and distal landmarks, and how spatial memory develops in the investigated age groups. Ten 5-year-old, ten 7-year-old and ten 10-year-old children were presented with the 'Kiel Locomotor Maze', containing features of the Radial Arm Maze and the Morris Water Maze, in order to assess spatial memory and orientation. Children had to learn to approach baited locations only. Task difficulty was equated with respect to the children's age. Training was given until the children reached criterion. During testing, the maze configuration and response requirements were systematically altered, including response rotation, cue rotation, cue deletion and response rotation with cue deletion in order to assess the spatial strategies used by the children. During training and testing, working-memory errors (WM), reference-memory errors (RM) and working-reference memory errors (WR) were recorded. As expected, no difference between age groups appeared during training, thus confirming comparable task difficulty across age groups. During testing, age groups differed significantly with regard to the orientation strategy used. The 5-year-olds were bound to a cue strategy, orientating towards local, proximal cues. The 10-year-olds mastered all tasks, thus displaying a place strategy, being able to use distal cues for orientation, and were even able to do so after being rotated 180 degrees. The 7-year-olds proved to be at an age of transition: five of them were bound to a cue strategy, five children were able to adopt a place strategy. The differences in the orientation strategies used by children of different age groups was reflected by the sum of errors they made, also by RM. WM were found to be rare, especially in older children. We conclude that preschoolers use a cue strategy, that the development of place strategies occurs during primary school age and seems to be complete by the age of 10 years.

Age Factors↗
PubMed2003

Detection and discrimination of texture modulations defined by orientation, spatial frequency, and contrast.

We sought to determine whether the detection and the identification of texture modulations are mediated by a common mechanism. On each trial two textures were presented, one of which contained a modulation in orientation (OM), spatial frequency (FM), or contrast (CM). Observers were required to indicate whether the modulated texture was presented in the first or the second interval as well as the nature of the texture modulation. The results showed that for two of the three pairwise matchings (OM-FM and OM-CM) detection and identification performance were nearly identical, suggesting a common underlying mechanism. However, when FM and CM textures were paired, discrimination thresholds were significantly higher than detection thresholds. In the context of the filter-rectify-filter model of texture perception, our results suggest that the mechanisms underlying detection are labeled with respect to their first-order input; i.e., the identities of these mechanisms are available to higher levels of processing. Several possible explanations for the misidentification of FM and CM at detection threshold are considered.

Contrast Sensitivity↗
PubMed2000

The functional role of oriented spatial filters in the perception of mirror symmetry--psychophysics and modeling.

We investigated human sensitivity to vertical mirror symmetry in noise patterns filtered for narrow bands of variable orientations. Sensitivity is defined here as the amount of spatial phase randomization corresponding to 75% correct performance in a 2AFC detection task. In Experiment 1, sensitivity was found to be high for tests patterns of all orientations except those parallel to the axis of symmetry. This implies that corresponding mirror-orientations (e.g. -45 and +45 degrees ) are combined prior to symmetry detection. In Experiment 2, observers detected symmetry in tests of variable orientation in the presence of either non-symmetric or symmetric masks filtered for orientations either parallel or perpendicular to the axis. Observers were found to be primarily affected by masks of the same orientation as the test, thus suggesting that symmetry is computed separately in distinct mirror-orientation channels. In Experiment 3, observers detected a symmetric test of variable height and width embedded in random noise. Data revealed that mirror symmetry is computed over a spatial integration region (IR) that remains approximately constant in area but whose height-to-width aspect ratio changes from 20:1 to 2:1 as orientation is varied from parallel to perpendicular to the axis. We compare human data against that of an ideal observer to identify key factors that limit visual performance and discuss the implications for the functional architecture of symmetry perception. We also propose a multi-channel model of symmetry detection that combines the output of oriented spatial filters in a simple and physiologically plausible manner. Particular emphasis is placed on the notion that changes in the shape of the IR with orientation compensate for changes in information density and partially equate performance across orientations.

Humans↗
PubMedDate not supplied

[Correlation of the visual and spatially oriented behaviors of white rats following the elaboration of a visual differentiation habit].

Correlation of spatial-motor and visually oriented reactions of white rats was studied by the method of three-side choice. It is shown that after acquisition of the habit of visual differentiation the visual orientation dominates only at taking feeding decision of passing to the passage. The choice of the direction of running to blinds and the choice of place of entering the passage do not depend on present visual signals location and do not reflect the state of visual differentiation habit, but are controlled by spatial memory.

Animals↗
PubMed2000

[Effects of knowledge acquisition on verbal linearization about spatial orientation].

This paper deals with determinants of linearization in spatial communication. The well-known linearization principles, such as the principle of natural order, primarily emphasize features of the given information. We assume that verbal linearization is in addition influenced by the speakers' knowledge acquisition. Six experiments with a total of 272 participants are reported here. A particular spatial constellation was presented to the participants, who were asked to talk about it afterwards. The linearizations then produced were defined as dependent variables. The results show that the linearizations were influenced by the speaker's experience with the configuration (according-to-experience effect) and also demonstrate the importance of the first encounter (anchor effect). Further characteristics of the effects mentioned above are described and discussed regarding memory research and psycho-linguistics.

Adult↗
PubMed1986

Spatial orientation of the mitotic apparatus and its stability in a polarized epithelial cell. A computer-assisted morphometric analysis.

The spatial and temporal orientation of the mitotic apparatus in reference to the polarized structure of an epithelial cell, as well as the relationship between mitotic spindle positioning and the direction of epithelial cell migration, was investigated. As an experimental model the epithelium of the mouse small intestine was chosen. Computer-assisted morphometric analysis applied in this study disclosed that the position of the mitotic spindle axis is restricted to a plane which is perpendicular to the axis of cell polarity. On this plane the spindle axis may occupy a random position. The latter finding indicates that there exists no correlation between the orientation of the mitotic spindle and the direction of epithelial cell migration. The plane of the spindle axis is established at metaphase, and no repositioning at further stages of mitosis has been observed. It is suggested that cell polarity plays a role in determination and stabilization of the mitotic spindle orientation in epithelial cells.

Animals↗
PubMed2001

[The "tunnel task": a method for examination of cognitive processes in spatial orientation performance].

We report on the theoretical development and empirical testing of a new spatial cognition task, during which participants complete a tour through a virtual tunnel. Upon arrival they are asked to specify a "homing" vector by pointing an arrow towards the starting point of their virtual journey. Systematic experimental variations include number, length and sharpness of turns. Solving the task requires the development of a spatial representation, as alternative strategic cues (e.g., visual landmarks) are not available. Performance measures discriminate between general training effects and specific task variables. As an example, "side errors" indicate a loss of orientation and "position hits" reflect the accuracy of the spatial representation. Participants use either an egocentric or allocentric frame of reference. The task does not imply the use of egocentric vs. allocentric spatial co-ordinates, yet it allows for a reliable a-priori identification of individually preferred strategies. Our data indicate that the spatial representations formed by both groups are functionally equivalent. However, the groups differ with respect to specific patterns of orientation errors.

Adult↗
PubMed2003

Anterior and posterior attentional control systems use different spatial reference frames: ERP evidence from covert tactile-spatial orienting.

To investigate whether processes controlling preparatory covert shifts of spatial attention operate within external and anatomically defined spatial coordinates, lateralized event-related potentials components sensitive to the direction of attentional shifts were measured in response to visual precues directing attention to the relevant location of tactile events. Participants had to detect infrequent tactile targets delivered to the hand located on the cued side. In different blocks, hands were uncrossed or crossed, so that external and anatomical codes specifying task-relevant locations were either congruent or incongruent. With uncrossed hands, an anterior directing attention negativity and a posterior directing attention positivity were elicited in the cue-target interval contralateral to the side of a cued attentional shift. Although the posterior effect was unaffected by hand posture, the anterior effect was delayed and reversed polarity with crossed relative to uncrossed hands. This pattern of results provides new evidence that different spatial coordinate systems may be used by separable attentional control processes. It is suggested that a posterior process operates on the basis of external spatial coordinates, whereas an anterior process is based primarily on anatomically defined spatial codes.

Adult↗
PubMed2001

Motion-surface labeling by orientation, spatial frequency and luminance polarity in 3-D structure-from-motion.

A compelling percept of three-dimensionality is attainable from a purely motion-defined simulation of a transparent rotating cylinder, referred to as 3-D structure-from-motion (SFM). Interestingly, subjects rarely perceive reversals of the cylinder's direction of rotation when they are introduced. Treue, Andersen, Ando, and Hildreth (Vision Res. 35 (1995) 139-148) have argued that this reflects the visual system's insensitivity to the textural detail on the cylinder's motion surfaces. We have recently shown however that with cylinders made from oriented micropatterns, motion reversals are perceived when the orientations of the micropatterns are different on the cylinder's front/back surfaces, suggesting that the visual system is sensitive to the type of feature in these stimuli (Vision Res. 39 (1999) 881-886). In the present study we extended this finding by testing for feature-sensitivity along other dimensions besides orientation, specifically spatial frequency, colour and luminance polarity. We found that subjects perceived more rotation direction reversals when the front/back surfaces of the cylinder were segregated, as opposed to non-segregated by feature-type, along all of these dimensions except, notably, colour. We also investigated the stage at which the feature-sensitivity is incorporated in 3-D SFM. We reasoned that if 3-D SFM mechanisms were tuned, or labeled for feature-type, swapping of features during the cylinder's rotation would result in illusory reversals in just the feature-segregated condition, whereas if grouping of like-features preceded the formation of 3-D motion surfaces, no such illusory reversals would be expected. We found that feature-swapping resulted in more illusory reversals in the feature-segregated compared to non-segregated conditions, supporting the mechanism tuning, or labeling, hypothesis.

Color Perception↗
PubMed2000

The time course of spatial orienting elicited by central and peripheral cues: evidence from event-related brain potentials.

To study differences in the time course of attentional orienting triggered by salient peripheral events and by central symbolic precues, event-related brain potentials (ERPs) were recorded in response to letter stimuli following spatially informative symbolic or peripheral precues after a cue-target interval (CTI) of either 200 or 700 ms. Stimuli at cued (attended) locations elicited an enhanced negativity relative to stimuli at uncued locations. With short CTIs, these effects started around 150 ms post-stimulus for peripheral cues. They were delayed by about 100 ms for central cues. This latency difference is assumed to reflect fast exogenous orienting elicited by peripheral, but not by central cues. Beyond 200 ms post-stimulus, attentional negativities were larger with long CTIs than with short CTIs for both cue types, presumably related to the gradual build-up of endogenous orienting triggered by spatially predictive events.

Adolescent↗
PubMed1997

Spatial orientation in humans: perception of angular whole-body displacements in two-dimensional trajectories.

Vestibular perception of whole-body passive rotation in the horizontal plane was studied by applying two-dimensional (2D) motion to eight blindfolded healthy volunteers: pure rotations in place, corner-like trajectories and arcs of a circular trajectory were randomly applied by means of a remotely controlled robot. Angles embedded in the 2D trajectories were 45 degrees, 90 degrees, 135 degrees and 180 degrees. Stimulation of semicircular canals was the same for all trajectories but was accompanied by concurrent otolith stimulation during circular motion. Subjects participated in two successive experimental sessions. In the first session they were instructed to use a pointer to reproduce the total angular displacement after the motion (REPRODUCTION); in the second session they had to keep pointing towards a remote (15 m) memorised target during the motion (TRACKING). In REPRODUCTION subjects tended to overestimate their rotation angle by 28 +/- 11% (mean +/- SD). There was no systematic effect of the trajectory. Overestimation also occurred when subjects were required to rotate in darkness by 180 degrees (by controlling a joystick). In TRACKING there was virtually no overestimation (6 +/- 17%) and the movement of the pointer matched the dynamics of angular motion. We conclude that (a) the brain can separate and memorise the angular component of complex 2D motion; however, a large inter-individual variability in estimating its amplitude exists; (b) in the range of linear accelerations used in the study, no appreciable effect of otolith-canal perceptual interaction was shown; (c) angular displacements can be dynamically transformed into matched pointing movements; (d) overestimation seems to be typical of delayed judgements of angular displacement and of self-controlled rotations in place. This could be due to the characteristics of the physiological calibration of the vestibular input.

Humans↗
PubMedDate not supplied

[A comparative analysis of spatial orientation in a changing environment in rats with differing preliminary experience].

Comparison of rats behaviour with different preliminary experience in elaboration of the strategy of return to place of reinforcement was conducted. Significant differences in the number of selective replacements to the place of reinforcement in previous tests in experienced, inexperienced and naive rats were found. It was proved that decisive role in the appearance of the found differences played gained experience and the process of engram extraction from memory. Inhibition of search in naive rats and ability to selective use of strategies corresponding to situation in the experienced ones in condition of stress of permanent changes were shown.

Adaptation, Physiological↗