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Interactions between phasic alerting and spatial orienting: effects of normal aging and Alzheimer's disease.

The effects of aging and Alzheimer's disease (AD) on phasic alerting and exogenous spatial orienting were examined within a single precuing task. Phasic alerting decreased with normal aging and was completely eliminated with AD. AD patients also demonstrated an increased spatial orienting effect, attributable to an increased benefit from spatial orienting that was associated with a decreased benefit from nonselective alerting. These results suggest that performance within the precuing paradigm reflects the product of an interaction between nonselective alerting processes and spatially selective orienting processes. The results also highlight the importance of simultaneously assessing alerting and orienting within the same task, because changes attributable to alerting may otherwise be attributed incorrectly to changes in 1 or more processes associated with spatial orienting.

Adolescent↗

The dynamics of spatial orientation during complex and changing linear and angular acceleration.

The dynamics of spatial orientation perception were examined in a series of experiments in which a total of 43 subjects were passively exposed to various combinations of linear and angular acceleration during centrifuge runs. Perceptual effects during deceleration were much stronger than effects during acceleration. The dynamics of spatial orientation perception differed substantially from changes in the vestibulo-ocular reflex (VOR). VOR was fairly well predicted by a current model, but our experiments revealed perceived change in attitude (roll, pitch, yaw tilt position in space) and perceived angular velocity in space that was not reflected by parallel changes in the plane or magnitude of the VOR. This series of experiments establishes several facts concerning spatial orientation perception beyond the predictive domain of any current model. New concepts are needed and several are suggested to deal with changing reactions to complex combinations of linear and angular accelerations.

Acceleration↗

Contribution of vestibular commissural pathways to spatial orientation of the angular vestibuloocular reflex.

During nystagmus induced by the angular vestibuloocular reflex (aVOR), the axis of eye velocity tends to align with the direction of gravito-inertial acceleration (GIA), a process we term "spatial orientation of the aVOR." We studied spatial orientation of the aVOR in rhesus and cynomolgus monkeys before and after midline section of the rostral medulla abolished all oculomotor functions related to velocity storage, leaving the direct optokinetic and vestibular pathways intact. Optokinetic afternystagmus and the bias component of off-vertical-axis rotation were lost, and the aVOR time constant was reduced to a value commensurate with the time constants of primary semicircular canal afferents. Spatial orientation of the aVOR, induced either during optokinetic or vestibular stimulation, was also lost. Vertical and roll aVOR time constants could no longer be lengthened in side-down or supine/prone positions, and static and dynamic tilts of the GIA no longer produced cross-coupling from the yaw to pitch and yaw to roll axes. Consequently, the induced nystagmus remained entirely in head coordinates after the lesion, regardless of the direction of the resultant GIA vector. Gains of the aVOR and of optokinetic nystagmus to steps of velocity were unaffected or slightly increased. These results are consistent with a model in which the direct aVOR pathways are organized in semicircular canal coordinates and spatial orientation is restricted to the indirect (velocity storage) pathways.

Animals↗

Tactile influences on astronaut visual spatial orientation: human neurovestibular studies on SLS-2.

Human spatial orientation in spaceflight is initially disturbed by the absence of usable graviceptor information from the otolithic organs. Experiments measuring astronaut visually induced motion (vection) strength on various flight days during the first 10 days of the Spacelab Life Sciences-2 mission demonstrated two new phenomena in addition to confirming the initial increased weighting of visual and localized tactile cues. The reliance on tactile and visual noninertial cues apparently declined after a week in space, as the crew became able to utilize their internal reference frame. Subjects also showed that even nondirectional tactile cues served as a direction anchor and inhibited visually induced roll sensation relative to a new loosely tethered test condition. Individual perceptual styles were again revealed among the four astronauts tested. The readaptation to 1 G similarly shows a period of reinterpretation of inertial and visual cues to spatial orientation. The results are discussed in terms of an internal-model representation of body orientation, with time-varying weights applied to extrinsic and intrinsic signals.

Adult↗

Evidence of temporal lobe activation by discriminative spatial orientation.

The results from this spatial orientation, or cue priming, investigation found that targets presented to the contralateral visual fields differentially activated the temporal zones. For instance, stimulation within the right visual field lead to activation of the left temporal zones, as indexed by the relative prominence of the association negativity, N2. The converse was true for left visual field stimulation. For both visual field stimulation, the N2 component also showed an occipital and parietal distribution. The P300 component, which is presumed to be modulated by medial temporal lobe structures, showed the classic centroparietal distribution. Somewhat surprisingly, differences between the primed (e.g., 'facilitated') and 'normal' conditions for the N2 component appeared restricted to the occipital zones. Here, the significant variable was the N2 peak latency. Hence, the priming cue appears to quicken the maximal development of the N2 processing component, preferentially over the occipital cortex, and this may partially explain the faster reaction times in the 'facilitated' conditions for both visual fields.

Adult↗

Visual-spatial orienting in autism.

Visual-spatial orienting in high-functioning adults with autism and both chronological- and mental-age normal controls was examined. Three experiments were conducted in which stimuli were presented centrally and/or laterally (left or right of central fixation), and either detection or identification was required. The group with autism differed from normal controls by responding faster to central than to lateral stimuli, and by showing a left visual field advantage for stimulus detection only in the simplest condition (lateral presentations alone). Discussion focuses on the apparent abnormalities in disengaging/shifting attention, and on the coordination of attentional and motor systems in autism.

Adult↗

Some contributions of touch, pressure and kinesthesis to human spatial orientation and oculomotor control.

Human spatial orientation and oculomotor control are under multimodal influence. It is not possible in the normal animal to stimulate differentially the vestibular receptors without activating other receptor systems whose activity may have a profound influence on postural control and experienced orientation. Many patterns of behavior and response that have been attributed solely to vestibular function are actually dependent wholly or in part on touch, kinesthetic, and proprioceptive stimulation.

Eye Movements↗

Resolving perceptual conflicts: the cognitive mechanism of spatial orientation.

The cognitive mechanisms of spatial orientation were studied in an experiment varying different perceptual cues systematically: the retinal, the visual background, the vestibular, and the somatosensory information. Verbal descriptions of visually presented arrays were required under different head positions (straight/tilt) and under different gravity conditions (1 G/micro G). Results for two subjects clearly show that different coordinate systems are used under the two gravity conditions. Under 1 G it is the gravitational vertical which is chosen for primary reference, whereas under microgravity retinal information is primary. Conflicts between competing pieces of sensory information are solved by weighting the perceptual cues differently. The finding that consistent assignment can be made immediately after first exposure to weightlessness indicates that mental representations of space can be used independently of perceptual input parameters.

Cognition↗

The role of left-right symmetry in the encodement of spatial orientations.

Three experiments investigated a hypothesis, suggested by studies of the difficulties of discriminating between shapes forming symmetrical pairs, that spatial orientations of thin flat plates (lamellae) may be encoded in a plane, the encodement consisting of two enantiomorphs. The results indicated that participants encoded the spatial orientation of lamellar stimuli in terms of the difference in cogency between their two enantiomorphic elements (Expt 1). The difference in the cogency of the two enantiomorphs is related to the orientation of the plane containing the lamellar stimulus with respect to the participant's fronto-parallel plane (Expt 2). The two possible orientations of a lamella which yield the same difference of cogency, but which differ in spatial orientation (e.g. lamella 'b' set at 30 degrees or set at 150 degrees) are distinguished by the manner in which the two enantiomorphic elements are arranged with respect to their axis of symmetry (Expt 3). The results suggest that the orientation of a lamella may be encoded as a two-dimensional representation and hence that three dimensions may be encoded by two by means of enantiomorphs. Implications of this finding for the encodements of three-dimensional solids, wherein pronounced contours may fulfil the same role as do the edges of lamella, are discussed briefly.

Adult↗

Spatial orientation in aviation: visual contributions.

Misjudgment of spatial orientation is reported to be an important factor in a substantial proportion of aviation accidents. The likelihood of such misjudgment is particularly high when there are conflicting interactions between labyrinthine and visual signals. In a manoeuvering aircraft, visual information is often a crucial factor in the pilot's ability to judge the aircraft's altitude and position with respect to external and terrain features. A body of research evidence supports the following conceptual framework. (1) The human visual system processes a limited number of visual dimensions almost independently of each other (for example, colour, luminance, spatial frequency, orientation, changing size, motion in depth, time to contact). (2) Each of these selective sensitivities shows considerable intersubject variability. (3) Intersubject variability is far from perfectly correlated across the set of selective sensitivities. This paper discusses the relevance of this framework for predicting, first the specific situations in which visual judgments are most likely to occur and, second, which individual pilots are most likely to make the visual misjudgments.

Accidents, Aviation↗

Multisensory integration in spatial orientation.

Recent psychophysical studies on normal subjects, as well as brain imaging studies, have revised the concepts concerning the mechanisms underlying spatial orientation during navigation tasks. The emphasis has been put on internal models that allow the prediction of a planned trajectory and are essential in the steering of locomotion. Cognitive factors such as strategies and emotional parameters are now starting to be included in the research on spatial orientation. It is obvious that important individual and gender differences exist in the brain operations underlying spatial orientation in humans, which may help to understand the construction of a coherent perception and the organic neural disorders related to the internal representation of space.

Emotions↗

Set-shifting and spatial orientation in patients with Parkinson's disease.

Individuals with Parkinson's disease were compared to normal control subjects on a series of widely used neuropsychological measures. The two groups were matched for gender, handedness, age, education, and occupation. The neuropsychological tests were chosen to measure two specific functions: (a) spatial orientation (i.e., measures of personal orientation, extrapersonal orientation, right/left orientation, and mental rotation), and (b) the ability to shift mental set (e.g., generating responses from alternating categories). The tests chosen to measure spatial orientation had no set-shifting component, and the tests chosen to measure set-shifting had no spatial orientation component. Multivariate statistical analyses revealed a significant difference between the subjects with Parkinson's disease and the control subjects on the measures of set-shifting ability. In contrast, no significant difference between the groups was observed on the measures of spatial orientation. These results are discussed in terms of the current speculation in the literature regarding the relationship between set-shifting deficits and a disruption of dopaminergic fibers to the prefrontal cortex in Parkinson's disease.

Aged↗

The Gap effect for spatially oriented responses.

The gap effect refers to the finding that a temporal gap between fixation point offset and target onset typically results in shorter saccadic latencies than if the fixation point remains on. Recently, this gap effect was found for aimed hand movements as well as saccadic eye movements, but not for simple keypress responses. In order to examine the hypothesis that the hand gap effect occurs for different types of spatially oriented movements, two experiments were conducted. In the first experiment, subjects produced spatially oriented responses to a peripheral target and the target location was known in advance of the targets presentation. This spatially oriented detection task yielded gap effects for both eye and hand responses. In the second experiment, the duration of the temporal gap was varied between 0-400 ms. The duration of the temporal gap had similar effects on the magnitudes of both the eye and hand gap effects, suggesting that a common mechanism may underlie the gap effect for saccadic and manual pointing movements. Overall, the results of the present experiments confirm the finding of a gap effect for spatially oriented hand movements and suggest that this effect may be related to the functioning of the superior colliculus.

Fixation, Ocular↗

Spatial orientation in the lamprey. I. Control of pitch and roll

Two major tasks must be fulfilled during locomotion: propulsion and spatial orientation. In the lamprey, the propulsive force is generated by laterally directed body undulations propagated from the rostral to the caudal end of the body. The neuronal networks underlying this basic locomotor pattern have been described in considerable detail. The present study was undertaken to provide the necessary behavioural background for parallel studies of the vestibular neuronal networks responsible for spatial orientation during locomotion. The following results were obtained. 1. The lamprey actively stabilized its pitch angle during swimming and usually kept a linear trajectory in the sagittal plane, despite large changes in the speed of swimming. During repeated tests, a certain preferred pitch angle could be maintained over a period of several minutes, even if the initial starting angle of the animal was changed considerably. 2. Two different strategies were observed for active turning in the downward direction: a smooth turn accomplished by weak ventral flexion of the whole body, and a sharp turn accomplished by localized ventral flexion of a region of the body just posterior to the gills. 3. The lampreys were oriented with the dorsal side up while swimming at any pitch angle. The control systems for pitch and roll can thus operate independently. When swimming, lampreys kept the tail region flexed somewhat ventrally. This body configuration will cause lateral movements of the tail to generate a torque that rotates the body around its longitudinal axis. This mechanism is presumably used to correct deviations from the dorsal-side-up orientation. After amputation of the dorsal and tail fins, lampreys maintained a proper spatial orientation during swimming. 4. After a unilateral labyrinthectomy, swimming lampreys continuously rolled towards the lesioned side. Unilaterally labyrinthectomized animals displayed a tonic twisting of the body into a helical shape. This presumably represents an additional strategy for performing roll turns. Bilaterally labyrinthectomized animals never maintained a linear trajectory in any plane, but turned continuously in all directions.

Journal Article↗

Spatial orientation mechanisms and their implications for falls.

Postural stability is only one function on a multisensory system that also subserves spatial orientation and gaze stability. The problem of falling is discussed in the context of understanding the nature and integration of these sensory loops, and the possibility of their modification is discussed. The characteristics of the visual system contributing to spatial orientation are analyzed. The role of gaze stability in postural balance and its modification as a function of age are also discussed. It is suggested that our understanding of the problem of falling will be enhanced by a research strategy that views the problem as a special case of spatial orientation.

Accidents↗

[Memory and visuo-spatial orientation disorders in children with contusions and compression of the brain in the acute period of the injury].

Characteristics of disorders of aural and speech memory and visual-spatial orientation were studied in 70 children aged 5-14 years at the acute period of brain injuries and compressions. Neuropsychic examination was conducted according to Luria's scheme including the technique of memory evaluation and test to evaluate spatial orientation. Disorders of memory and spatial orientation were correlated with the severity of the head trauma and the predominant localization of the brain injury.

Adolescent↗