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PubMed2000

The contributions of slant and tilt to the detection of local surface orientation in structure from motion.

The contribution of slant and tilt to the detection of differences in local surface orientation was examined for structure-from-motion (SFM) displays of a complex sinusoidal surface. Observers judged whether an elliptical SFM gauge figure appeared to be lying on the surface or intersecting it. The gauge figure orientation either matched the local surface orientation or differed from it in slant, tilt, or both. Similar sensitivity was found for deviations in slant and tilt, but greater biases and variability were found when the gauge figure deviated from the local surface orientation in slant, depending on the sign of the difference between the gauge figure and local surface orientation and the position of the gauge figure. The results are consistent with Stevens' (Biological Cybernetics, 46 (1983) 183-195) discussion of the computational advantages of slant and tilt contributing independently to the detection of differences in local surface orientation. The effects of changes in perceived surface slant and tilt during rotation and of the misperception of surface depth on the detection of local orientation in dynamic images are discussed.

Female↗
PubMed2002

Orthogonal adaptation and orientation discrimination.

The change in apparent orientation of lines and gratings induced by surrounding or preceding patterns of a different orientation (the tilt illusion and tilt after-effect) has been abundantly documented, but there is no unanimity about the effect of such inducing patterns on orientation discrimination thresholds. In particular, because inducing contours that are almost orthogonal cause the direction of the tilt illusion to reverse, evidence for an improvement of orientation discrimination with orthogonal adaptation has been welcomed on theoretical ground as supporting concepts of inversion of polarity of neural connection between cortical cells with oriented receptive fields for large orientation differences. In careful psychophysical experiments on human observers with several kinds of test and orthogonal adaptation patterns the average ratio of adapted/unadapted discrimination thresholds in paired sets of data was 1.027+/-0.13, which does not differ significantly from unity and hence constitutes evidence that orthogonal adaptation does not improve orientation discrimination.

Adaptation, Physiological↗
PubMed2002

Latency effects in orientation popout.

A target that differs in orientation from neighboring lines and "pops out" has been found to evoke larger responses in cortical V1 cells than lines in the uniform texture surround which do not popout (e.g., Journal of Neurophysiology 67 (1992) 961). If this is more than a coincidence of observations, physiological properties of contextual modulation should be reflected in the perception of salience. In particular, as the differential suppression from texture surround has been reported to be delayed, target salience may be affected by the history of surrounding lines, i.e. by their orientation before the target was presented. This was tested using a feature flicker paradigm in which target and background lines changed their orientations (Experiment 2). All subjects (N = 4) indicated a benefit in target detection when target orientation was not previously present in the surround. A control experiment showed that this effect was not caused by the purely temporal aspects of asynchronous stimulus presentation (Experiment 3). To distinguish this effect from other sources of delayed processing, Experiment 1 compared the performance in target detection and target identification tasks, for single-lines and popout targets. All subjects required longer stimulus presentation time to identify the orientation of a single line than to detect the line itself, indicating that orientation coding needs longer processing than encoding stimulus onset. However, most subjects needed even longer presentations to detect popout, suggesting that the processing of orientation contrast adds to this delay. In an appendix, putative response variations of V1 cells to asynchronous flicker are computed.

Adult↗
PubMed2000

Further experiments on the relationship between hippocampus and orientation following phase-shift in homing pigeons.

Following a clock- or phase-shift of the light dark cycle, hippocampal lesioned pigeons (Columba livia) consistently display a larger deviation in vanishing bearings away from the homeward direction compared to intact birds; an effect never seen in unshifted birds. In Experiment 1, control and hippocampal lesioned pigeons oriented similarly after being held 1 week under artificial lighting in the absence of a phase-shift. Housing under artificial light by itself does not result in between group orientation differences. In Experiment 2, control and hippocampal lesioned pigeons oriented equally well under overcast conditions, indicating that both groups had a functional magnetic compass. The between group difference in orientation following phase-shift does not appear to be a consequence of control birds being able to use both the sun and earth's magnetic field for orientation and the hippocampal lesioned pigeons only being able to use the sun. In Experiment 3, lengthening the time held under 6-h clock-shift from 1 to 2 weeks had no effect on the magnitude of the difference in orientation, but fast shifting produced clearer effects than slow shifting. Taken together, the data suggest that hippocampal lesions alter how a pigeon responds to a rapidly changing light-dark cycle, particularly following a fast-shift manipulation, suggesting an as yet unspecified relationship between the avian hippocampus and the circadian rhythm(s) that regulate sun compass orientation.

Animals↗
PubMed1999

Effects of lesion of pontomedullary reticular formation on visually triggered vertical and oblique head orienting movements in alert cats.

The role of the nucleus reticularis pontis caudalis (NRPC) and the nucleus reticularis gigantocellularis (NRG) in control of vertical and oblique head orienting movements was investigated in alert cats by lesion of these nuclei with kainic acid. Cats were trained to orient the head vertically or obliquely to various targets. Following unilateral lesion of these nuclei, vertical orienting could be performed correctly with a slight decrease in velocity, while oblique orienting tended to exhibit zigzag course because of severe impairment of horizontal orienting. The horizontal and vertical components became coordinated in the course of experiments due to a significant decrease in vertical component velocity, resulting in smooth oblique trajectories. Results suggest that horizontal and vertical components of head orienting are controlled separately, but impairment of horizontal component causes adaptive change of vertical component velocity in oblique orienting.

Adaptation, Physiological↗
PubMed1998

The contribution of intracortical inhibition to dynamics of orientation tuning in cat striate cortex neurons.

Orientation tuning of some neurons in cat visual cortex (area 17) revealed successive shifts of the preferred orientation and widening of tuning in time during the first 150 ms after onset of a flashing light bar. The mechanisms of these dynamics and the possible role of intracortical inhibition are still under discussion. In this study we analysed the dynamics using the time slice method before and during blockade of GABAergic inhibition by microiontophoretic application of bicuculline and observed two main types of neuronal behaviour. The first group of neurons (39 of 68 units or 57.4%) with relatively sharp tuning and absence or relatively small shifts of preferred orientation under control conditions increased or developed this shift during bicuculline application. Changes in tuning were observed between 30 and 150 ms after stimulus onset when inhibition was blocked. Neurons of the second group (29 units or 42.6% of cases) displayed pronounced shifts of preferred orientation under control conditions which was typically diminished or lost during blockade of inhibition. The results indicate different contributions of intracortical inhibition to different neurons distinguishing by stability or time dependence of their orientation preference during normal response generation. In one group of striate cells orientation tuning was kept narrow and constant in time by intracortical inhibition, while in another group orientation tuning dynamics are induced by inhibitory mechanisms.

Animals↗
PubMed1997

Relationships between local synaptic connections and orientation domains in primary visual cortex.

Combined optical imaging of ferret primary visual cortex in vivo and scanning laser photostimulation in brain slices were used to determine the spatial relationships between synaptic inputs onto individual neurons and the pattern of orientation columns. In the upper cortical layers, both excitatory and inhibitory inputs originated primarily from regions with orientation tuning similar to that of the recorded neurons; the shapes of the input tuning curves were indistinguishable. The orientation distributions of both types of inputs centered around the orientation of the recorded neurons, and no evidence for preferential cross-orientation inputs, either excitatory or inhibitory, was observed. These patterns of synaptic connectivity are most consistent with feedforward models for generation of orientation selectivity and are inconsistent with the patterns required by models based on cross-orientation inhibition.

Animals↗
PubMed2002

Early involvement of the temporal area in attentional selection of grating orientation: an ERP study.

The aim of the present study was to investigate the neural mechanisms of stimulus orientation selection in humans by recording event-related potentials (ERPs) of the brain with a 32-channel montage. Stimuli were isoluminant black-and-white gratings (3 cpd) having an orientation of 50, 70, 90, 110 and 130, randomly presented in the foveal portion (2 of visual angle) of the central visual field. The task consisted in selectively attending and responding to one of the five grating orientations, while ignoring the others. ERP results showed that orientation selection affected neural processing starting already at an early post-stimulus latency. The P1 component (80-140 ms) measured at temporal area, which might well be reflecting the activity of the ventral stream (i.e. 'WHAT' system) of the visual pathways, showed an enhanced amplitude for target orientations. These effects increased with progressive neural processing over time as reflected by selection negativity (SN) and P300 components. In addition, both reaction times (RTs) and ERPs showed a strong 'oblique' effect, very probably reflecting the perceptual predominance of orthogonal versus oblique stimulus orientation in the human visual system: RTs were much faster, and SN and P300 components much larger, to gratings presented vertically than in other orientations.

Adult↗
PubMed1982

Orientation-specific visual evoked potential deficits in multiple sclerosis.

Checkerboard pattern reversal visual evoked potentials (VEPs) have proved useful in the confirmation of optic nerve disease in patients with multiple sclerosis (MS). Recently evidence of orientation-specific loss in contrast sensitivity and the presence of orientation-specific visual evoked potential (VEP) deficits in MS patients has been obtained using sinusoidal gratings as stimuli. This study reports the presence of orientation-specific VEP delay in MS using the conventional checkerboard pattern presented in two orientations: normally oriented (check condition) or diagonally oriented (diamond condition). Peak latency values of the N70 and P100 components of the VEP were statistically analyzed using appropriate ANOVA and nonparametric statistics. As a group of MS patients showed significant VEP delays under check and diamond pattern conditions. However, individual subject analysis revealed that about 20% of the MS population show VEP delay to only one pattern orientation. It was shown that by including a diamond pattern condition the diagnostic yield of VEP delay in these clinically definite MS patients was increased 11% over that obtained with check stimulation alone.

Electroretinography↗
PubMedDate not supplied

Optical imaging of orientation and ocular dominance maps in area 17 of cats with convergent strabismus.

Strabismus (or squint) is both a well-established model for developmental plasticity of the brain and a frequent clinical symptom. While the layout and topographic relationship of functional domains in area 17 of divergently squinting cats has been analyzed extensively in recent years (e.g. Löwel et al., 1998), functional maps in convergently squinting animals have so far not been visualized with comparable detail. We have therefore investigated the functional organization of area 17 in adult cats with a surgically induced convergent squint angle. In these animals, visual acuity was determined by both behavioral tests and recordings of visual evoked potentials, and animals with comparable acuities in both eyes were selected for further experiments. The functional layout of area 17 was visualized using optical imaging of intrinsic signals. Monocular iso-orientation domains had a patchy appearance and their layout was different for left and right eye stimulation, so that segregated ocular dominance domains could be visualized. Iso-orientation domains exhibited a pinwheel-like organization, as previously described for normal and divergently squinting cats. Mean pinwheel density was the same in the experimental and control animals (3.4 pinwheel centers per mm2 cortical surface), but significantly (P < 0.00001) higher than that reported previously for normal and divergently squinting cats (2.7/mm2). A comparison of orientation with ocular dominance maps revealed that iso-orientation domains were continuous across the borders of ocular dominance domains and tended to intersect these borders at steep angles. However, in contrast to previous reports in normally raised cats, orientation pinwheel centers showed no consistent topographical relationship to the peaks of ocular dominance domains. Taken together, these observations indicate an overall similarity between the functional layout of orientation and ocular dominance maps in area 17 of convergently and divergently squinting cats. The higher pinwheel densities compared with previous reports suggest that animals from different gene pools might generally differ in this parameter and therefore also in the space constants of their cortical orientation maps.

Animals↗
PubMedDate not supplied

A model for the intracortical origin of orientation preference and tuning in macaque striate cortex.

We report results of numerical simulations for a model of generation of orientation selectivity in macaque striate cortex. In contrast to previous models, where the initial orientation bias is generated by convergent geniculate input to simple cells and subsequently sharpened by lateral circuits, our approach is based on anisotropic intracortical excitatory connections which provide both the initial orientation bias and its subsequent amplification. Our study shows that the emerging response properties are similar to the response properties that are observed experimentally, hence the hypothesis of an intracortical generation of orientation bias is a sensible alternative to the notion of an afferent bias by convergent geniculocortical projection patterns. In contrast to models based on an afferent orientation bias, however, the "intracortical hypothesis" predicts that orientation tuning gradually evolves from an initially nonoriented response and a complete loss of orientation tuning when the recurrent excitation is blocked, but new experiments must be designed to unambiguously decide between both hypotheses.

Animals↗
PubMed1989

Orientation specificity in spatial memory: what makes a path different from a map of the path?

Three studies investigated the factors that lead spatial information to be stored in an orientation-specific versus orientation-free manner. In Experiment 1, we replicated the findings of Presson and Hazelrigg (1984) that learning paths from a small map versus learning the paths directly from viewing a world leads to different functional characteristics of spatial memory. Whether the route display was presented as the path itself or as a large map of the path did not affect how the information was stored. In Experiment 2, we examined the effects of size of stimulus display, size of world, and scale transformations on how spatial information in maps is stored and available for use in later judgments. In Experiment 3, we examined the effect of size on the orientation specificity of the spatial coding of paths that are viewed directly. The major determinant of whether spatial information was stored and used in an orientation-specific or an orientation-free manner was the size of the display. Small displays were coded in an orientation-specific way, whereas very large displays were coded in a more orientation-free manner. These data support the view that there are distinct spatial representations, one more perceptual and episodic and one more integrated and model-like, that have developed to meet different demands faced by mobile organisms.

Adult↗
PubMed2005

Orienting to eye gaze and face processing.

The author conducted 7 experiments to examine possible interactions between orienting to eye gaze and specific forms of face processing. Participants classified a letter following either an upright or inverted face with averted, uninformative eye gaze. Eye gaze orienting effects were recorded for upright and inverted faces, irrespective of whether the faces were simple, schematic faces or more realistic faces. In contrast, inversion affected orienting to targets appearing along the vertical axis. Switching the contrast between the iris and sclera reversed orienting to eye gaze. Lifting the eyelid to expose more of the iris-sclera contrast led to a potentiation of orienting to eye gaze. Raising the eyebrow alone without the eyelid did not affect orienting. The findings suggest that local perceptual information is critical for orienting to eye gaze and that the effect can occur with a degree of independence from certain types of face processing.

Adolescent↗
PubMed2004

A morphological basis for orientation tuning in primary visual cortex.

Feedforward connections are thought to be important in the generation of orientation-selective responses in visual cortex by establishing a bias in the sampling of information from regions of visual space that lie along a neuron's axis of preferred orientation. It remains unclear, however, which structural elements-dendrites or axons-are ultimately responsible for conveying this sampling bias. To explore this question, we have examined the spatial arrangement of feedforward axonal connections that link non-oriented neurons in layer 4 and orientation-selective neurons in layer 2/3 of visual cortex in the tree shrew. Target sites of labeled boutons in layer 2/3 resulting from focal injections of biocytin in layer 4 show an orientation-specific axial bias that is sufficient to confer orientation tuning to layer 2/3 neurons. We conclude that the anisotropic arrangement of axon terminals is the principal source of the orientation bias contributed by feedforward connections.

Animals↗
PubMed1988

Interactions in the discrimination and absolute judgement of orientation and length.

An asymmetric model is described for interactions in the perception of two dimensions (length and orientation) of a single visual stimulus. Two methods were used to test these interactions, and models for the interpretation of the possible outcomes of these tests are discussed. A length discrimination task showed facilitation (decreased reaction time) when orientation was covaried with length, and interference (increased reaction time) when random orientation variation was introduced. A smaller effect was seen when length was varied in an orientation discrimination task in a correlated or random fashion. Analysis of sequential effects showed that reaction times are fastest on repetition trials and are slowed by either the need to change the response or the need for additional sensory processing. With the second method, it was found that the amount of information transmitted in the estimation of orientation was not affected by the introduction of the redundant dimension of length, but that there was a significant gain in the amount of information transmitted in the estimation of length by the addition of the redundant dimension of orientation. It is concluded that orientation is probably a perceptual primitive of the visual system whereas length is a computed variable.

Adult↗
PubMed1989

Errors in estimating the orientation of dot patterns.

The error in estimating the orientation of a dot pattern was measured as the difference between the orientation of the least-squared-distances line (LS-line) of the pattern and the orientation of a line adjusted by the subject to match the perceived orientation of the pattern. Analysis of the mean errors (averaged over ten subjects) obtained for one hundred patterns confirmed that the orientation of the LS-line represents the orientation of elongated dot-patterns. It is shown that estimated orientation was systematically biased towards the nearest 45 degrees oblique meridian. This bias points to the importance of the +/-45 degrees directions as natural norms for left- and right-side tilt in the frontoparallel plane.

Adult↗
PubMed1989

An orientation anisotropy in induced brightness.

It is shown that an orientation anisotropy exists for the magnitude of induced brightness in a cruciform stimulus consisting of a grey test patch positioned at the intersection of two inducing bars, one black and one white, oriented at right angles to each other. When the cruciform was oriented such that the white bar was horizontal, the grey patch appeared darker than when the same cruciform was oriented such that the white bar was vertical. The contribution of the black and white inducing bars towards the brightness of the test patch was investigated. A simple mathematical function, which took into account both the contribution of the two component inducing bars and the orientation anisotropy, was fitted to the data. No consistent orientation anisotropy was found with inducing stimuli at oblique orientations.

Attention↗
PubMed1999

Hierarchical organisation in perception of orientation.

According to Rock [1990, in The Legacy of Solomon Asch (Hillsdale, NJ: Lawrence Erlbaum Associates)], hierarchical organisation of perception describes cases in which the orientation of an object is affected by the immediately surrounding elements in the visual field. Various experiments were performed to study the hierarchical organisation of orientation perception. In most of them the rod-and-frame-illusion (RFI: change of the apparent vertical measured on a central rod surrounded by a tilted frame) was measured in the presence/absence of a second inner frame. The first three experiments showed that, when the inner frame is vertical, the direction and size of the illusion are consistent with expectancies based on the hierarchical organisation hypothesis. An analysis of published and unpublished data collected on a large number of subjects showed that orientational hierarchical effects are independent from the absolute size of the RFI. In experiments 4 to 7 we examined the perceptual conditions of the inner stimulus (enclosure, orientation, and presence of luminance borders) critical for obtaining a hierarchical organisation effect. Although an inner vertical square was effective in reducing the illusion (experiment 3), an inner circle enclosing the rod was ineffective (experiment 4). This indicates that definite orientation is necessary to modulate the illusion. However, orientational information provided by a vertical or horizontal rectangle presented near the rod, but not enclosing it, did not modulate the RFI (experiment 5). This suggests that the presence of a figure with oriented contours enclosing the rod is critical. In experiments 6 and 7 we studied whether the presence of luminance borders is important or whether the inner upright square might be effective also if made of subjective contours. When the subjective contour figure was salient and the observers perceived it clearly, its effectiveness in modulating the RFI was comparable to that observed with luminance borders.

Adult↗