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Results for “Spatial orientation”

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At least 703 records · Page 39Linked to original sources

PubMed1999

Visual adaptation as optimal information transmission.

We propose that visual adaptation in orientation, spatial frequency, and motion can be understood from the perspective of optimal information transmission. The essence of the proposal is that neural response properties at the system level should be adjusted to the changing statistics of the input so as to maximize information transmission. We show that this principle accounts for several well-documented psychophysical phenomena, including the tilt aftereffect, change in contrast sensitivity and post-adaptation changes in orientation discrimination. Adaptation can also be considered on a longer time scale, in the context of tailoring response properties to natural scene statistics. From the anisotropic distribution of power in natural scenes, the proposal also predicts differences in the contrast sensitivity function across spatial frequency and orientation, including the oblique effect.

Adaptation, Ocular↗

PubMed2005

Control networks and hemispheric asymmetries in parietal cortex during attentional orienting in different spatial reference frames.

Neuropsychological research has consistently demonstrated that spatial attention can be anchored in one of several coordinate systems, including those defined with respect to an observer (viewer-centered), to the gravitational vector (environment-centered), or to individual objects (object-centered). In the present study, we used hemodynamic correlates of brain function to investigate the neural systems that mediate attentional control in two competing reference frames. Healthy volunteers were cued to locations defined in either viewer-centered or object-centered space to discriminate the shape of visual targets subsequently presented at the cued locations. Brain responses to attention-directing cues were quantified using event-related functional magnetic resonance imaging. A fronto-parietal control network was activated by attention-directing cues in both reference frames. Voluntary shifts of attention produced increased neural activity bilaterally in several cortical regions including the intraparietal sulcus, anterior cingulate cortex, and the frontal eye fields. Of special interest was the observation of hemispheric asymmetries in parietal cortex; there was significantly greater activity in left parietal cortex than in the right, but this asymmetry was more pronounced for object-centered shifts of attention, relative to viewer-centered shifts of attention. Measures of behavioral performance did not differ significantly between the two reference frames. We conclude that a largely overlapping, bilateral, cortical network mediates our ability to orient spatial attention in multiple coordinate systems, and that the left intraparietal sulcus plays an additional role for orienting in object-centered space. These results provide neuroimaging support for related claims based on findings of deficits in object-based orienting in patients with left parietal lesions.

Adolescent↗

PubMed2006

Impact of vision on the development of topographical orientation abilities.

The current experiment examined the importance of visual input on the construction of inner spatial representations. Early and late-onset blind and paired control participants performed a tactile spatial orientation task. No significant group differences were observed, indicating that the blind can represent space. More errors, however, were committed by the early blind than by the late blind and sighted individuals in portions of the task that involved mental rotation skills, suggesting a potential facilitating role for vision in the proper development of spatial constructs.

Adult↗

PubMed2000

Spatial cognition and neuro-mimetic navigation: a model of hippocampal place cell activity.

A computational model of hippocampal activity during spatial cognition and navigation tasks is presented. The spatial representation in our model of the rat hippocampus is built on-line during exploration via two processing streams. An allothetic vision-based representation is built by unsupervised Hebbian learning extracting spatio-temporal properties of the environment from visual input. An idiothetic representation is learned based on internal movement-related information provided by path integration. On the level of the hippocampus, allothetic and idiothetic representations are integrated to yield a stable representation of the environment by a population of localized overlapping CA3-CA1 place fields. The hippocampal spatial representation is used as a basis for goal-oriented spatial behavior. We focus on the neural pathway connecting the hippocampus to the nucleus accumbens. Place cells drive a population of locomotor action neurons in the nucleus accumbens. Reward-based learning is applied to map place cell activity into action cell activity. The ensemble action cell activity provides navigational maps to support spatial behavior. We present experimental results obtained with a mobile Khepera robot.

Animals↗

PubMed2005

Does swarming cause honey bees to update their solar ephemerides?

Spatial orientation in the social insects offers several examples of specialized learning mechanisms that underlie complex learning tasks. Here we study one of these systems: the processes by which honey bees update, or fail to update, their memories of the sun's daily pattern of movement (the solar ephemeris function) in relation to the landscape. Specifically, we ask whether bees that have initially learned the solar ephemeris function relative to a conspicuous treeline at their natal site can later realign the ephemeris to a differently oriented treeline. We first confirm and clarify an earlier finding that bees transplanted passively (by being carried) do not re-learn the solar ephemeris in relation to the new treeline. When they cannot detect the sun directly, as on overcast days, these transplanted bees use a solar ephemeris function appropriate for their natal site, despite days or weeks of experience at the new site. We then ask whether bees put through a swarming process as they are transplanted are induced to re-learn the solar ephemeris function at the new site, as swarming is a natural process wherein bees transplant themselves. Most of the swarmed bees failed to re-learn, even though they did extensive learning flights (in comparison with those of non-swarmed controls) as they first emerged from the hive at the new site. We hypothesize that the bees' representation of the solar ephemeris function is stored in an encapsulated cognitive module in which the ephemeris is inextricably linked to the reference landscape in which it was learned.

Animal Communication↗

PubMedDate not supplied

[Conditioned reflex activity in the aging process in white rats].

In Wistar rats, irrespectively of their age, conditioned reflexes to present stimuli are preserved and elaborated. Neither the mechanism of time intervals estimation is disturbed in aged and old rats (24-32 months). Long intervals between experiments (3-5 months) do not influence their state. Distinct changes are revealed of spatial-temporal differentiations in T-maze: significant worsening of their state is observed in 8-10 months age; in this age it is neither possible to elaborate them again. In simplified experimental conditions in the T-maze the old rats preserve the spatial orientation.

Acoustic Stimulation↗

PubMed1998

Where and when to pay attention: the neural systems for directing attention to spatial locations and to time intervals as revealed by both PET and fMRI.

Although attention is distributed across time as well as space, the temporal allocation of attention has been less well researched than its spatial counterpart. A temporal analog of the covert spatial orientation task [Posner MI, Snyder CRR, Davidson BJ (1980) Attention and the detection of signals. J Exp Psychol Gen 109:160-174] was developed to compare the neural systems involved in directing attention to spatial locations versus time intervals. We asked whether there exists a general system for allocating attentional resources, independent of stimulus dimension, or whether functionally specialized brain regions are recruited for directing attention toward spatial versus temporal aspects of the environment. We measured brain activity in seven healthy volunteers by using positron emission tomography (PET) and in eight healthy volunteers by using functional magnetic resonance imaging (fMRI). The task manipulated cued attention to spatial locations (S) and temporal intervals (T) in a factorial design. Symbolic central cues oriented subjects toward S only (left or right), toward T only (300 msec or 1500 msec), toward both S and T simultaneously, or provided no information regarding S or T. Subjects also were scanned during a resting baseline condition. Behavioral data showed benefits and costs for performance during temporal attention similar to those established for spatial attention. Brain-imaging data revealed a partial overlap between neural systems involved in the performance of spatial versus temporal orientation of attention tasks. Additionally, hemispheric asymmetries revealed preferential right and left parietal activation for spatial and temporal attention, respectively. Parietal cortex was activated bilaterally by attending to both dimensions simultaneously. This is the first direct comparison of the neural correlates of attending to spatial versus temporal cues.

Adult↗

PubMed2006

Reoxygenation with 100% oxygen versus room air: late neuroanatomical and neurofunctional outcome in neonatal mice with hypoxic-ischemic brain injury.

Study investigated neuroutcome in mice subjected at 7-8 d of life to hypoxic-ischemic brain injury (HI) followed by 30 min of reoxygenation with 100% O(2) (Re-O(2)) or room air (Re-Air). At 24 h of recovery, mouse reflexes were tested. At 7 wks after HI spatial orientation and memory were assessed in the same mice. Mortality rate was recorded at 24 h and at 7 wks of recovery. In separate cohort of mice, changes in cerebral blood flow (CBF) during HI-insult and reoxygenation were recorded. Re-O(2)versus Re-Air mice exhibited significantly delayed geotaxis reflex. Adult Re-O(2)versus Re-Air mice exhibited significantly better spatial learning and orientation with strong tendency toward better preserved memory. Histopathology revealed significantly less hippocampal atrophy in Re-O(2)versus Re-Air mice. Following a hypoxia-induced hypoperfusion, Re-O(2) re-established CBF in the ipsilateral side to the prehypoxic level significantly faster than Re-Air. The mortality was higher among Re-O2 versus Re-Air mice, although, it did not reach statistical significance. Re-O(2)versus Re-Air restores CBF significantly faster and results in better late neuroutcome. However, greater early motor deficit and higher mortality rate among Re-O(2)versus Re-Air mice suggest that Re-O(2) may be deleterious at the early stage of recovery.

Air↗

PubMed1999

The stereoscopic (cyclopean) motion aftereffect is selective for spatial frequency and orientation of disparity modulation.

Across two experiments, this study investigated the spatial frequency tuning and orientation tuning (both in the disparity domain) of the stereoscopic (cyclopean) motion aftereffect. In Experiment 1, observers adapted to a moving stereoscopic grating of a given cyclopean spatial frequency and tested for the motion aftereffect with a static grating of the same or different spatial frequency. Robust motion aftereffects were induced only when the spatial frequency of the adapt and test stimuli was the same. In Experiment 2, observers adapted to a moving stereoscopic grating of a given cyclopean orientation and tested for the motion aftereffect with a static grating of the same or different orientation. Robust motion aftereffects were induced only when the orientation of the adapt and test stimuli was the same. Together, these results suggest that the stereoscopic motion aftereffect is tuned for cyclopean spatial frequency and orientation which, in turn, suggest that the stereoscopic motion aftereffect is mediated by low-level oriented spatial-frequency mechanisms.

Adaptation, Physiological↗

PubMed1988

A model of spatial localization and its application to strabismus.

Visually guided, spatially oriented behavior involves an ongoing integration of signals regarding the loci of the retinal images and the position and orientation of the eye. In the strabismic this requires an altered spatial metric resulting from a functional readaptation to avoid confusion and diplopia. A comparator mechanism for evaluating these two signals is presented. A case report using "disruptive" therapeutic procedures that deliberately alter the strabismic's visual-postural control system is presented. A treatment plan for altering the anomalous binocular link, a characteristic of the well adapted strabismic, is described and related to the comparator mechanism.

Adaptation, Physiological↗

PubMed2006

Chimpanzees (Pan troglodytes) remember the location of a hidden food item after altering their orientation to a spatial array.

Two chimpanzees (Pan troglodytes) had a direct view of an experimenter placing a food item beneath one of several cups within a horizontal spatial array. The chimpanzees then were required to move around the spatial array, shifting their orientation to the array by 180 degrees . Both chimpanzees remembered the location of the food item. In the next experiment, a visual barrier was placed between the chimpanzees and the spatial array after the food item had been hidden to prevent visual tracking of the location of the object during the chimpanzees' movement. One chimpanzee remembered the location of the hidden item in this variation. These results demonstrate another capacity for spatial memory in this species that complements data indicating chimpanzee spatial memory for invisible displacements, array rotations, and array transpositions.

Animals↗

PubMed1999

Local inhibition of hippocampal nitric oxide synthase does not impair place learning in the Morris water escape task in rats.

Recent studies have provided evidence that nitric oxide (NO) has a role in certain forms of memory formation. Spatial learning is one of the cognitive abilities that has been found to be impaired after systemic administration of an NO-synthase inhibitor. As the hippocampus has a pivotal role in spatial orientation, the present study examined the role of hippocampal NO in spatial learning and reversal learning in a Morris task in adult rats. It was found that N omega-nitro-L-arginine infusions into the dorsal hippocampus affected the manner in which the rats were searching the submerged platform during training, but did not affect the efficiency to find the spatial location of the escape platform. Hippocampal NO-synthase inhibition did not affect the learning of a new platform position in the same water tank (i.e. reversal learning). Moreover, no treatment effects were observed in the probe trials (i.e. after acquisition and after reversal learning), indicating that the rats treated with N omega-nitro-L-arginine had learned the spatial location of the platform. These findings were obtained under conditions where the NO synthesis in the dorsal hippocampus was completely inhibited. On the basis of the present data it was concluded that hippocampal NO is not critically involved in place learning in rats.

Animals↗

PubMed2001

Magnetic compass orientation in the blind mole rat Spalax ehrenbergi.

The blind mole rat Spalax ehrenbergi is a solitary, subterranean rodent that digs and inhabits a system of branching tunnels, with no above-ground exits, which it never leaves unless forced to. To survive, the mole rat must be able to orient efficiently in its tunnel system. The sensory channels available for spatial orientation in the subterranean environment are restricted in comparison with those existing above ground. This study examined the possibility that the mole rat is able to perceive and use the earth's magnetic field to orient in space. Experiments were performed using a device constructed from a pair of electromagnetic 'Helmholtz coils', which create a magnetic field whose direction and strength can be altered. In the first experiment, we tested a group of mole rats (N=33) in an eight-armed maze under the earth's natural magnetic field to determine whether they have directional preferences for the location of their sleeping nest, food chamber and toilet site. A second group of mole rats (N=30) was tested for their directional preference after the earth's magnetic field had been experimentally shifted by 180 degrees. We found that the first group exhibited a significant preference (P<0.001) to build both their sleeping nest and their food store in the southern sector of the maze, whereas the second group shifted the location of their nests (P<0.01) and food store (P<0.05), to the northern sector of the maze, corresponding to the shift in the magnetic field. In the second experiment, we tested whether the magnetic compass orientation found in the first experiment depends on a light stimulus by testing a group of mole rats in the eight-armed maze under total darkness. No significant difference in directional preference between light and dark test conditions was observed. It can be concluded, therefore, that, in contrast to some amphibians and birds, magnetic compass orientation in the mole rat is independent of light stimulation. In the third experiment, we examined whether mole rats (N=24) use the earth's magnetic field as a compass cue to orient in a labyrinth. In the first stage (trials 1-13), the animals were trained to reach a goal box at the end of a complex labyrinth until all individuals had learned the task. In the second stage (trial 14), half the trained mole rats underwent another labyrinth trial under the earth's natural magnetic field, while the other half were tested under a magnetic field shifted by 180 degrees. We found a significant decrease (P<0.001) in performance of the mole rats tested under the shifted magnetic field compared with the group tested under the natural magnetic field. The findings from these experiments prove that the mole rat is able to perceive and use the earth's magnetic field to orient in space.

Animals↗

PubMed1985

Reduction of body sway by stimuli imaged within a cortical scotoma: a case study.

The reduction of body sway by visual stimulation was equally effective for stimuli imaged within a cortical scotoma or in the mirror image position in the normal visual field. The results are consistent with the concept of distinct visual orientation and discrimination modes of processing visual information, which suggests that spatial orientation functions do not necessarily involve awareness.

Adult↗

PubMed1999

Motion streaks provide a spatial code for motion direction.

Although many neurons in the primary visual cortex (V1) of primates are direction selective, they provide ambiguous information about the direction of motion of a stimulus. There is evidence that one of the ways in which the visual system resolves this ambiguity is by computing, from the responses of V1 neurons, velocity components in two or more spatial orientations and then combining these velocity components. Here I consider another potential neural mechanism for determining motion direction. When a localized image feature moves fast enough, it should become smeared in space owing to temporal integration in the visual system, creating a spatial signal-a 'motion streak'-oriented in the direction of the motion. The orientation masking and adaptation experiments reported here show that these spatial signals for motion direction exist in the human visual system for feature speeds above about 1 feature width per 100 ms. Computer simulations show that this psychophysical finding is consistent with the known response properties of V1 neurons, and that these spatial signals, when appropriately processed, are sufficient to determine motion direction in natural images.

Computer Simulation↗

PubMed2000

Idiothetic orientation and path integration in unilateral hippocampal atrophy and sclerosis.

We determined the effects of hippocampal lesions on idiothetic spatial orientation by exposing 14 patients with unilateral hippocampal atrophy and/or sclerosis (HAS) and 10 normal controls to random rotational displacements (+/-30 degrees -180 degrees ) in darkness and examined their ability to rotate themselves back to the initial position. In comparison to controls, the patients responses were distinctly hypometric (p<0.005). Patients with right hippocampal lesions showed a trend towards higher come back errors p = 0.08). Normal controls could maintain their accuracy over five consecutive trials. Patients, beginning with less accuracy, showed significant improvement after each trial (p<0.001). The findings suggest that unilateral HAS impair the immediate recall of idiothetic spatial information, but does not affect long-term spatial learning.

Adult↗

PubMed1994

Spatial scale shifts in amblyopia.

We used a masking paradigm to uncover the properties of the mechanisms engaged by the amblyopic visual system for vernier acuity and line detection. Line vernier and line detection thresholds were measured in the presence of one-dimensional noise masks varying in orientation, spatial frequency content or contrast. Our results reveal that in both normal and amblyopic eyes, there is a bimodal orientation tuning function for vernier acuity, i.e. vernier acuity is most strongly masked by mask orientations approx. +/- 10 deg on either side of the target lines. In contrast, in both normal and amblyopic eyes, line detection is most strongly masked when the mask and line target have the same orientation. In the normal fovea, the spatial frequency tuning is bandpass, with a peak spatial frequency of about 10 c/deg. In the amblyopic eyes, the spatial tuning is similar in specificity; however the peak is shifted to lower spatial frequencies, suggesting a shift in the scale of spatial processing of line stimuli. For all of the amblyopic eyes, the increased line detection thresholds are approximately proportional to the shift in spatial scale. In anisometropic amblyopes, the (unmasked) vernier threshold is elevated in proportion to the shift in spatial scale; however in some amblyopes with constant strabismus the shift in spatial scale is not sufficient to account for the degraded vernier acuity. The "extra" increase in vernier thresholds associated with strabismus may be a consequence of a high degree of positional uncertainty which adds noise at a stage following the combination of filter responses.

Adult↗

PubMed1997

Magnetic orientation and the magnetic sense in arthropods.

The physical properties of the earth's magnetic field are summarized with the aim of emphasizing their significance as cues that can be exploited in orientational tasks. Past work has revealed magnetic orientation in vertebrates as well as invertebrates, including arthropods. The key finding to date has been that, as opposed to many vertebrates, the magnetic compass of arthropods responds to the polarity, rather than to the inclination of the earth's magnetic field. As in the case of vertebrates, the debate over how arthropods detect magnetic fields has yet to be resolved. Currently, evidence has been reported in support of a detection system based on magnetite crystals together with a variety of detection systems based on events occurring at the molecular level. Interactions between the magnetic and other compasses in orientation experiments suggest the existence of an area in the brain where spatial orientation information from magnetic and other stimuli converges. The slow advance of our knowledge on magnetic orientation in arthropods, as opposed to the much better understanding of magnetic orientation in vertebrates, arises from difficulties in identifying the appropriate behavioural contexts in which arthropods respond to magnetic fields in both laboratory and field situations. Arthropods thus present challenges not only in demonstrating magnetic orientation, but also in elucidating the sensory mechanisms involved in the perception of magnetic fields.

Animals↗