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Spatial interactions in apparent contrast: inhibitory effects among grating patterns of different spatial frequencies, spatial positions and orientations.

Suppression of the apparent contrast of a small 4 cycle wide suprathreshold sine wave grating patch by a high contrast sine wave grating surround pattern was studied as a function of the spatial frequency, orientation and spatial extent of the surround. The data are consistent with the existence of a complex network of inhibitory interconnections among mechanisms that mediate contrast perception. These connections must extend over spatial distances equivalent to more than 12 cycles of the central grating patch.

Adaptation, Physiological↗

The antennal system and cockroach evasive behavior. I. Roles for visual and mechanosensory cues in the response.

Cockroaches escape from predators by turning and then running. This behavior can be elicited when stimuli deflect one of the rostrally located and highly mobile antennae. We analyzed the behavior of cockroaches, under free-ranging conditions with videography or tethered in a motion tracking system, to determine (1) how antennal positional dynamics influence escape turning, and (2) if visual cues have any influence on antennal mediated escape. The spatial orientation of the long antennal flagellum at the time of tactile stimulation affected the direction of resultant escape turns. However, the sign of flagellar displacement caused by touch stimuli, whether it was deflected medially or laterally for example, did not affect the directionality of turns. Responsiveness to touch stimuli, and escape turn performance, were not altered by blocking vision. However, because cockroaches first orient an antenna toward stimuli entering the peripheral visual field, turn direction can be indirectly influenced by visual input. Finally, when vision was blocked, the run phase of escape responses displayed reduced average velocities and distances traveled. Our results suggest that tactile and visual influences are integrated with previously known wind-sensory mechanisms to achieve multisensory control of the full escape response.

Animals↗

Spacial perception and spatial memory in children with benign childhood epilepsy with centro-temporal spikes (BCECTS).

Despite the benign prognosis regarding the response of seizures to treatment, some evidence now exists that patients with benign childhood epilepsy with centro-temporal spikes (BCECTS) may have neuropsychological deficits sometimes leading to academic underachievement. There is, however, no general agreement on the exact profile of functions disturbed. This study was designed to identify significant deficits in spatial perception and memory in children with BCECTS (ages 6-10 years) compared with healthy controls matched for age, sex and socioeconomic status. The neuropsychological test battery administered consisted of the HAWIK-III, the "Tübinger Luria Christensen Neuropsychological Test Set for Children", the "Kaufman Assessment Battery for Children" and the "Differential Neuropsychological Test". Twenty-two patients and 22 control subjects completed all tests. Children with BCECTS exhibited significant deficits in higher functions of spatial perception, including spatial orientation, as well as in basal and complex spatial memory. Deficits were independent of the lateralization of the epileptogenic foci and independent of anti-convulsive drug treatment.

Case-Control Studies↗

Spatial invariance in anticipatory orienting behaviour during human navigation.

We have recently reported that the head systematically deviates toward the future direction of the trajectory about 500 ms before attaining a turning point of 90 degrees corner trajectories both in light and in darkness. Here, we investigated how this anticipatory strategy is modified whilst varying visual conditions (Experiment 1) and walking speed (Experiment 2). Exp. 1 showed similar anticipatory behaviour when walking with or without vision. Exp. 2 (that varied walking speed; eyes open) showed that the head started to deviate at a constant distance rather than at a constant time to the corner. The results appear inconsistent with optic flow theories of the guidance of walking direction and might highlight the role of landmarks and/or egocentric direction in anticipatory orienting behaviour.

Adult↗

The effects of unilateral pulvinar damage in humans on reflexive orienting and filtering of irrelevant information.

The effects of damage to the pulvinar nucleus of the thalamus in humans on reflexive orienting and selective attention were investigated. In a spatial orienting task three patients with unilateral pulvinar damage determined the location of a visual target that followed a cue that was not informative as to the targets location. Contralesional targets were responded to more slowly than ipsilesional targets. Also, at long cue target intervals patients responses to contralesional targets that appeared at previously cued locations were slower than to non-cued locations indicating that pulvinar damage does not affect inhibition of return. In the selective attention task two of the patients identified a target that appeared at one level of a global-local hierarchical stimulus while ignoring a distractor present at the other level. The distractor indicated either the same response as the target or a different response. Response times to targets in both visual fields were similar as were interference effects from the ignored distractors. These data indicate that engaging attention contralesionally is not impaired in discrimination tasks and that filtering of irrelevant information was not impaired contralesionally.

Attention↗

Oblique interaction of spatial dark-soliton stripes in nonlocal media.

We report what we believe to be the first experimental observation of a large spatial lateral shift in the interaction of obliquely oriented spatial dark-soliton stripes. We demonstrate by numerical simulations that this new effect can be attributed to the specific features of optical media with a nonlocal nonlinear response.

Journal Article↗

The processing of spatial frequency and orientation information.

Three identification experiments were completed to disambiguate the associations between spatial frequency and orientation information at the sensory, decisional, and response levels. The stimuli were gratings generated by crossing four levels each of spatial frequency and orientation. In Experiment 1, the subjects made a single identification response to the stimuli. In Experiment 2, two identification responses were made, one for the spatial frequency component and the other for the orientation component. In Experiment 3, the subjects identified either the spatial frequency or the orientation component in any block of trials. The data were confusion matrices, and an information-transmission approach was used to investigate the interactions in the system. The results show that although there were sensory associations, there were no interactions at the decisional level. Performance parity was found: there was no significant difference between the single- and double-judgment paradigms in terms of information transmitted. Overall, the results suggest that although spatial frequency and orientation information is coded jointly at the sensory level, subsequent processing is independent, with each dimension drawing upon different attentional resources.

Adult↗

Revisiting unilateral neglect.

Unilateral neglect, a neurological disorder in which patients fail to detect or respond to contralesional stimuli, has long been considered a failure of attentional orienting mechanisms. This review provides a selective overview of the prominent biases in spatial orienting and exploratory motor behaviour observed in these patients before considering the impact of other factors on the presentation of the disorder and how those factors might inform current neurological models of neglect. In the latter part of the review, we intend to suggest that neglect is likely to be a combination of distinct but interacting impairments including biases in attentional orienting, exploratory motor behaviours and a deficit of spatial working memory. That is, we suggest that the cardinal symptom of neglect - a loss of awareness for contralesional stimuli and events - arises as a result of a combination of these impairments rather than being associated solely with the more dramatic and immediately evident biases in spatial attention.

Animals↗

Orientation and diameter distribution of rabbit blood platelets flowing in small arterioles.

Spatial orientation of blood platelets flowing in small arterioles of the rabbit mesentery was investigated using intravital fluorescence microscopy. Only platelets were studied that could be localized objectively within a thin optical section around the median plane of the vessel. The orientation of a platelet was assessed from its microscopic image and described by an angle pair, assuming the platelet to be an ellipsoidal body and using an empirical frequency distribution for its thickness to diameter ratio. The orientation of the platelets was not random; they tended to align themselves with their equatorial planes parallel to the wall. The degree of alignment increased from the center of the vessel toward the wall. As a corollary a frequency distribution of their diameter (3.15 +/- 0.72 micron (mean +/- sd) was obtained in vivo.

Animals↗

Relationship between spatial-frequency and orientation tuning of striate-cortex cells.

If striate cells had the receptive-field (RF) shapes classically attributed to them, their preferred spatial frequencies would vary considerably with orientation. Other models of RF shape would predict a greater independence between orientation and spatial-frequency tuning. We have examined this by recording the responses of cat striate-cortex cells to a wide range of different spatial-frequency and orientation combinations. In almost all cells studied, peak orientation did not consistently vary with spatial frequency, but the majority of cells showed some change in peak spatial-frequency tuning with orientation. The amount of change in peak spatial frequency tended to be greater for cells that were narrowly tuned for orientation. However, cells narrowly (and also very broadly) tuned for spatial frequency tended to show considerable independence of spatial-frequency and orientation tuning, and in all but a few cells the degree of change was less than predicted by the classic RF model. Such cells were found to fire only to patterns whose local spatial spectra fell within a compact, restricted, roughly circular two-dimensional spatial-frequency region. We conclude that the two-dimensional RF shape of striate cells more closely approximates that predicted by a two-dimensional Gabor model or by a Gaussian-derivative model than it does the classic shape based on the output of geniculate cells with aligned RF's.

Animals↗

Relationship between orientation tuning and spatial frequency in neurones of cat area 17.

The orientation bandwidth was measured at different spatial frequencies for simple and complex cells. With increasing spatial frequency, the orientation tuning of simple cells became progressively narrower. This tendency was much less marked in complex cells. The results are interpreted in support of geniculate cells with orthogonal orientation biases providing the excitatory and inhibitory inputs to a simple cell.

Animals↗

Orientation and spatial-frequency discrimination for luminance and chromatic gratings.

We have examined the accuracy of orientation and spatial-frequency discrimination for sine-wave gratings that vary in either luminance or color. The equiluminant chromatic gratings were modulated along either a tritanopic confusion axis (so that they were detectable on the basis of activity in only the short-wavelength-sensitive cones) or an axis of constant short-wavelength-sensitive cone excitation (so that they could be detected on the basis of opposing activity in only the long- and medium-wavelength-sensitive cones). Grating contrasts ranged from the detection threshold to the highest levels that we could produce; the contrasts of the luminance and color patterns were equated for equal multiples of their respective detection thresholds. Discrimination thresholds for all patterns showed a similar dependence on stimulus contrast, rising sharply at low contrasts and becoming nearly asymptotic at moderate contrasts. However, even at threshold contrasts, observers could still reliably discriminate sufficiently large differences in the orientation or spatial frequency of all patterns, and they could also reliably identify the type of variation (luminance or which color) defining the grafting. For most conditions the discrimination thresholds did not differ from the two types of color grafting and reached values as low as 1 deg (orientation) or 4% (spatial frequency). Thus observers were able to make accurate spatial judgments on the basis of either type of chromatic information. However, these thresholds were slightly but consistently higher than the thresholds for comparable luminance graftings. This difference in the color and luminance discrimination thresholds may reflect somewhat coarser orientation and spatial-frequency selectivity in the mechanisms encoding the chromatic patterns.

Color Perception↗

Representation of spatial frequency and orientation in the visual cortex.

Knowledge of the response of the primary visual cortex to the various spatial frequencies and orientations in the visual scene should help us understand the principles by which the brain recognizes patterns. Current information about the cortical layout of spatial frequency response is still incomplete because of difficulties in recording and interpreting adequate data. Here, we report results from a study of the cat primary visual cortex in which we employed a new image-analysis method that allows improved separation of signal from noise and that we used to examine the neurooptical response of the primary visual cortex to drifting sine gratings over a range of orientations and spatial frequencies. We found that (i) the optical responses to all orientations and spatial frequencies were well approximated by weighted sums of only two pairs of basis pictures, one pair for orientation and a different pair for spatial frequency; (ii) the weightings of the two pictures in each pair were approximately in quadrature (1/4 cycle apart); and (iii) our spatial frequency data revealed a cortical map that continuously assigns different optimal spatial frequency responses to different cortical locations over the entire spatial frequency range.

Animals↗

The spatial properties of opponent-motion normalization.

The final stage of the Adelson-Bergen model [J. Opt. Soc. Am. A 2 (1985) 284] computes net motion as the difference between directionally opposite energies E(L) and E(R). However, Georgeson and Scott-Samuel [Vis. Res. 39 (1999) 4393] found that human direction discrimination is better described by motion contrast (C(m))--a metric where opponent energy (E(L)-E(R)) is divided by flicker energy (E(L)+E(R)). In the present paper, we used a lateral masking paradigm to investigate the spatial properties of flicker energy involved in the normalization of opponent energy. Observers discriminated between left and right motion while viewing a checkerboard in which half of the checks contained a drifting sinusoid and the other half contained flicker (i.e. a counterphasing sinusoid). The relative luminance contrasts of flicker and motion checks determined the checkerboard's overall motion contrast C(m). We obtained selectivity functions for opponent-motion normalization by measuring C(m) thresholds whilst varying the orientation, spatial frequency, or size of flicker checks. In all conditions, performance (percent correct) decayed lawfully as we decreased motion contrast, validating the C(m) metric for our stimuli. Thresholds decreased with check size and also improved as we increased either the orientation or spatial-frequency difference between motion and flicker checks. Our data are inconsistent with Heeger-type normalization models [Vis. Neurosci. 9 (1992) 181] in which excitatory inputs are normalized by a non-selective pooling of inhibitory inputs, but data are consistent with the implicit assumption in Georgeson and Scott-Samuel's model that flicker normalization is localized in orientation, scale, and space. However, our lateral masking paradigm leaves open the possibility that the spatial properties of flicker normalization would be different if opponent and flicker energies spatially overlapped. Further characterization of motion contrast will require models of the spatial, temporal, and joint space-time properties of mechanisms mediating opponent-motion and flicker normalization.

Contrast Sensitivity↗

Basal ganglia and gait control: apomorphine administration and internal pallidum stimulation in Parkinson's disease.

Gait coordination was analyzed (four-camera 100 Hz ELITE system) in two groups of idiopathic Parkinson disease (PD) patients. Five patients underwent continuous infusion of apomorphine and were recorded in two different sessions (APO OFF and APO ON) in the same day. Three patients with a previous chronic electrode implantation in both internal globi pallidi (GPi) were recorded in the same experimental session with the electrodes on and off (STIM ON and STIM OFF). The orientation of both the trunk and the lower-limb segments was described with respect to the vertical in the sagittal plane. Lower-limb inter-segmental coordination was evaluated by analyzing the co-variation between thigh, shank, and foot elevation angles by means of orthogonal planar regression. At least 30 gait cycles per experimental condition were processed. We found that the trunk was bent forward in STIM OFF, whereas it was better aligned with the vertical in STIM ON in both PD groups. The legs never fully extended during the gait cycle in STIM OFF, whereas they extended before heel strike in STIM ON. The multisegmental coordination of the lower limb changed almost in parallel with the changes in trunk orientation. In STIM OFF, both the shape and the spatial orientation of the planar gait loops (thigh angle vs. shank angle vs. foot angle) differed from those of physiological locomotion, whereas in STIM ON the gait loop tended to resume features closer to the control. Switching the electrodes on and off in patients with GPi electrodes resulted in quasi-parallel changes of the trunk inclination and of the planar gait loop. The bulk of the data suggest that the basal-ganglia circuitry may be relevant in locomotion by providing an appropriate spatio-temporal framework for the control of posture and movement in a gravity-based body-centered frame of reference. Pallido-thalamic and/or pallido-mesencephalic pathways may influence the timing of the inter-segmental coordination for gait.

Aged↗

Neuropsychology of selective attention and magnetic cortical stimulation.

Informed volunteers were asked to perform different neuropsychological tests involving selective attention under control conditions and during transcranial magnetic cortical stimulation. The tests chosen involved the recognition of a specific letter among different letters (verbal test) and the search for three different spatial orientations of an appendage to a square (visuo-spatial test). For each test the total time taken and the error rate were calculated. Results showed that cortical stimulation did not cause a worsening in performance. Moreover, magnetic stimulation of the temporal lobe neither modified completion time in both verbal and visuo-spatial tests nor changed error rate. In contrast, magnetic stimulation of the pre-frontal area induced a significant reduction in the performance time of both the verbal and visuo-spatial tests always without an increase in the number of errors. The experimental findings underline the importance of the pre-frontal area in performing tasks requiring a high level of controlled attention and suggest the need to adopt an interdisciplinary approach towards the study of neurone/mind interface mechanisms.

Adult↗

Selective learning and memory impairments in mice deficient for polysialylated NCAM in adulthood.

The neural cell adhesion molecule (NCAM) has been implicated in regulating synaptic plasticity mechanisms as well as memory consolidation processes. Attachment of polysialic acid to NCAM (PSA-NCAM) has been reported to down-regulate its adhesive forces, a process hypothesized to be implicated in synapse selection after learning experiences. PSA-NCAM has been critically implicated in hippocampus-related synaptic plasticity and memory storage, but information about its functional role in other brain areas remains scarce. Here, we studied mice deficient for polysialyltransferase-1 (ST8SialV/PST-1), an enzyme which attaches PSA to NCAM during postnatal development and adulthood, and whose deficiency results in a drastic reduction of PSA-NCAM expression throughout the brain in adulthood. Mice were tested for their performance in the water maze and auditory fear conditioning (AFC). We report that ST8SiaIV knockout mice were impaired in spatial as well as reversal learning in the water maze. On the other hand, AFC was intact and ST8SiaIV mice exhibited no impairments in the acquisition or retention of cued fear memories. Spatial orientation learning and reversal learning require complex integration of spatial information and response selection involving the hippocampus and prefrontal cortex, whereas cued fear conditioning is an associative type of emotional memory that highly depends on amygdala function. Therefore, our results indicate that PSA-NCAM contributes differentially to learning processes that differ in the nature of the neural computations involved, which probably reflects a differential role of this molecule in different brain regions.

Amygdala↗

Spatial-frequency and orientation tuning in psychophysical end-stopping.

A psychophysical analog to cortical receptive-field end-stopping has been demonstrated previously in spatial filters tuned to a wide range of spatial frequencies (Yu & Levi, 1997a). The current study investigated tuning characteristics in psychophysical spatial filter end-stopping. When a D6 (the sixth derivative of a Gaussian) target is masked by a center mask (placed in the putative spatial filter center), two end-zone masks (placed in the filter end-zones) reduce thresholds. This "end-stopping" effect (the reduction of masking induced by end-zone masks) was measured at various spatial frequencies and orientations of end-zone masks. End-stopping reached its maximal strength when the spatial frequency and/or orientation of the end-zone masks matched the spatial frequency and/or orientation of the target and center mask, showing spatial-frequency tuning and orientation tuning. The bandwidths of spatial-frequency and orientation tuning functions decreased with increasing target spatial frequency. At larger orientation differences, however, end-zone masks induced a secondary facilitation effect, which was maximal when the spatial frequency of end-zone masks equated the target spatial frequency. This facilitation effect might be related to certain types of contour and texture perception, such as perceptual pop-out.

Adult↗