Collinear effects on 3-Gabor alignment as a function of spacing, orientation and detectability.

Our ability to align three Gabor patches depends upon their internal carrier orientation; we are better at aligning vertical or horizontal patches than oblique patches (Keeble and Hess, 1998). However, the tuning of alignment to patch orientation has not studied in detail. We measured the alignment of a vertical target with reference patches varying in orientation and found it tuned to vertical (collinear) patches at centre-to-centre separation of three carrier periods, with a steep increase for oblique references and slight downturn for horizontal (orthogonal) references. Next, we increased separation between the patches, testing collinear, side-by-side, orthogonal and oblique configurations. Surprisingly, we found that the tuning for collinear patches was preserved. All ten observers tested had lower alignment thresholds for collinear patches. This effect extended to an inter-patch separation of 10 carrier periods (20 envelope standard deviations). Additionally, we measured contrast detection thresholds for the reference patches using the same stimuli. The collinear facilitation of alignment was even greater than the collinear facilitation of detection.     

Visual performance fields: frames of reference

Performance in most visual discrimination tasks is better along the horizontal than the vertical meridian (Horizontal-Vertical Anisotropy, HVA), and along the lower than the upper vertical meridian (Vertical Meridian Asymmetry, VMA), with intermediate performance at intercardinal locations. As these inhomogeneities are prevalent throughout visual tasks, it is important to understand the perceptual consequences of dissociating spatial reference frames. In all studies of performance fields so far, allocentric environmental references and egocentric observer reference frames were aligned. Here we quantified the effects of manipulating head-centric and retinotopic coordinates on the shape of visual performance fields. When observers viewed briefly presented radial arrays of Gabors and discriminated the tilt of a target relative to homogeneously oriented distractors, performance fields shifted with head tilt (Experiment 1), and fixation (Experiment 2). These results show that performance fields shift in-line with egocentric referents, corresponding to the retinal location of the stimulus.     

Horizontal-vertical filters in early vision predict anomalous line-orientation identification frequencies.

A characteristic of early visual processing is a reduction in the effective number of filter mechanisms acting in parallel over the visual field. In the detection of a line target differing in orientation from a background of lines, performance with brief displays appears to be determined by just two classes of orientation-sensitive filter, with preferred orientations close to the vertical and horizontal. An orientation signal represented as a linear combination of responses from such filters is shown to provide a quantitative prediction of the probability density function for identifying the perceived orientation of a target line. This prediction was confirmed in an orientation-matching experiment, which showed that the precision of orientation estimates was worst near the vertical and horizontal and best at about 30 degrees each side of the vertical, a result that contrasts with the classical oblique effect in vision, when scrutiny of the image is allowed. A comparison of predicted and observed frequency distributions showed that the hypothesized orientation signal was formed as an opponent combination and horizontal and vertical filter responses.     

Increased sensitivity to mirror symmetry in autism

Can autistic people see the forest for the trees? Ongoing uncertainty about the integrity and role of global processing in autism gives special importance to the question of how autistic individuals group local stimulus attributes into meaningful spatial patterns. We investigated visual grouping in autism by measuring sensitivity to mirror symmetry, a highly-salient perceptual image attribute preceding object recognition. Autistic and non-autistic individuals were asked to detect mirror symmetry oriented along vertical, oblique, and horizontal axes. Both groups performed best when the axis was vertical, but across all randomly-presented axis orientations, autistics were significantly more sensitive to symmetry than non-autistics. We suggest that under some circumstances, autistic individuals can take advantage of parallel access to local and global information. In other words, autistics may sometimes see the forest and the trees, and may therefore extract from noisy environments genuine regularities which elude non-autistic observers.     

Stochastic re-calibration: contextual effects on perceived tilt

The human visual system exaggerates the difference between the tilts of adjacent lines or grating patches. In addition to this tilt illusion, we found that oblique flanks reduced acuity for small changes of tilt in the centre of the visual field. However, no flanks--regardless of their tilts--decreased sensitivity to contrast. Thus, the foveal tilt illusion should not be attributed to orientation-selective lateral inhibition. Nor is it similar to conventional crowding, which typically does not impair letter recognition in the fovea. Our observers behaved as though the reference orientation (horizontal) had a small tilt in the direction of the flanks. We suggest that the extent of this re-calibration varies randomly over trials, and we demonstrate that this stochastic re-calibration can explain flank-induced acuity loss in the fovea.     

Apparent Motion from Outside the Visual Field,Retinotopic Cortices May Register Extra-Retinal Positions

Observers made a saccade between two fixation markers while a probe was flashed sequentially at two locations on a side screen. The first probe was presented in the far periphery just within the observer''s visual field. This target was extinguished and the observers made a large saccade away from the probe, which would have left it far outside the visual field if it had still been present. The second probe was then presented, displaced from the first in the same direction as the eye movement and by about the same distance as the saccade step. Because both eyes and probes shifted by similar amounts, there was little or no shift between the first and second probe positions on the retina. Nevertheless, subjects reported seeing motion corresponding to the spatial displacement not the retinal displacement. When the second probe was presented, the effective location of the first probe lay outside the visual field demonstrating that apparent motion can be seen from a location outside the visual field to a second location inside the visual field. Recent physiological results suggest that target locations are “remapped” on retinotopic representations to correct for the effects of eye movements. Our results suggest that the representations on which this remapping occurs include locations that fall beyond the limits of the retina.     

MPI CyberMotion Simulator: implementation of a novel motion simulator to investigate multisensory path integration in three dimensions

Path integration is a process in which self-motion is integrated over time to obtain an estimate of one's current position relative to a starting point (1). Humans can do path integration based exclusively on visual (2-3), auditory (4), or inertial cues (5). However, with multiple cues present, inertial cues - particularly kinaesthetic - seem to dominate (6-7). In the absence of vision, humans tend to overestimate short distances (<5 m) and turning angles (<30°), but underestimate longer ones (5). Movement through physical space therefore does not seem to be accurately represented by the brain. Extensive work has been done on evaluating path integration in the horizontal plane, but little is known about vertical movement (see (3) for virtual movement from vision alone). One reason for this is that traditional motion simulators have a small range of motion restricted mainly to the horizontal plane. Here we take advantage of a motion simulator (8-9) with a large range of motion to assess whether path integration is similar between horizontal and vertical planes. The relative contributions of inertial and visual cues for path navigation were also assessed. 16 observers sat upright in a seat mounted to the flange of a modified KUKA anthropomorphic robot arm. Sensory information was manipulated by providing visual (optic flow, limited lifetime star field), vestibular-kinaesthetic (passive self motion with eyes closed), or visual and vestibular-kinaesthetic motion cues. Movement trajectories in the horizontal, sagittal and frontal planes consisted of two segment lengths (1st: 0.4 m, 2nd: 1 m; ±0.24 m/s(2) peak acceleration). The angle of the two segments was either 45° or 90°. Observers pointed back to their origin by moving an arrow that was superimposed on an avatar presented on the screen. Observers were more likely to underestimate angle size for movement in the horizontal plane compared to the vertical planes. In the frontal plane observers were more likely to overestimate angle size while there was no such bias in the sagittal plane. Finally, observers responded slower when answering based on vestibular-kinaesthetic information alone. Human path integration based on vestibular-kinaesthetic information alone thus takes longer than when visual information is present. That pointing is consistent with underestimating and overestimating the angle one has moved through in the horizontal and vertical planes respectively, suggests that the neural representation of self-motion through space is non-symmetrical which may relate to the fact that humans experience movement mostly within the horizontal plane.     

Spatial location and hyperacuity: flank position within the centre and surround zones

Sensitivity to a horizontal displacement of a vertical line was measured in order to ascertain the influence of the location of parallel flanking lines on the apparent position of features in visual space. The first experiment confirmed that the introduction of the flank added a component to the apparent shift which was towards the flank for small separations (less than 3-4') and away from the flank with larger separations. The second experiment investigated the notion that apparent location is derived by collecting information only from zones adjacent to the target and limited in the vertical extent by the target's height i.e. information orthogonal to the target's main axis. This was done by placing a vertical flank at a horizontal distance from the target that would be clearly within one zone or the other and measuring the effect of a vertical separation between the two flank halves. In the surround zone the amount of repulsion obtained was not influenced by vertical separation of the flank halves, even when they were several minutes higher (or lower) than the target line. In the central zone attraction was only obtained when the vertical separation was small enough to provide some overlap of the lines in the horizontal direction. With larger separations substantial repulsion was obtained. We conclude that while the central 'attraction' zone may only use information distributed in the direction of the line's displacement, it does so only within a 3-4' range on either side of the target line. The surround zone is not similarly limited in the region over which it collects information to influence the apparent location of features.     

Interhemispheric connections shape subjective experience of bistable motion

The right and left visual hemifields are represented in different cerebral hemispheres and are bound together by connections through the corpus callosum. Much has been learned on the functions of these connections from split-brain patients [1-4], but little is known about their contribution to conscious visual perception in healthy humans. We used diffusion tensor imaging and functional magnetic resonance imaging to investigate which callosal connections contribute to the subjective experience of a visual motion stimulus that requires interhemispheric integration. The "motion quartet" is an ambiguous version of apparent motion that leads to perceptions of either horizontal or vertical motion [5]. Interestingly, observers are more likely to perceive vertical than horizontal motion when the stimulus is presented centrally in the visual field [6]. This asymmetry has been attributed to the fact that, with central fixation, perception of horizontal motion requires integration across hemispheres whereas perception of vertical motion requires only intrahemispheric processing [7]. We are able to show that the microstructure of individually tracked callosal segments connecting motion-sensitive areas of the human MT/V5 complex (hMT/V5+; [8]) can predict the conscious perception of observers. Neither connections between primary visual cortex (V1) nor other surrounding callosal regions exhibit a similar relationship.     

Stability of cortical responses and the statistics of natural scenes.

The primary visual cortex (V1) of higher mammals contains maps of stimulus features; how these maps influence vision remains unknown. We have examined the functional significance of an asymmetry in the orientation map in cat V1, i.e., the fact that a larger area of V1 is preferentially activated by vertical and horizontal contours than by contours at oblique orientations. Despite the fact that neurons tuned to cardinal and oblique orientations have indistinguishable tuning characteristics, cardinal neurons remain more stable in their response properties after selective perturbation induced by adaptation. Similarly, human observers report different adaptation-induced changes in orientation tuning between cardinal and oblique axes. We suggest that the larger cortical area devoted to cardinal orientations imposes stability on the processing of cardinal contours during visual perception, by retaining invariant cortical responses along cardinal axes.     

Experience shapes the utility of natural statistics for perceptual contour integration

Segmenting meaningful targets from cluttered scenes is a fundamental function of the visual system. Evolution and development have been suggested to optimize the brain's solution to this computationally challenging task by tuning the visual system to features that co-occur frequently in natural scenes (e.g., collinear edges) [1, 2, 3]. However, the role of shorter-term experience in shaping the utility of scene statistics remains largely unknown. Here, we ask whether collinearity is a specialized case, or whether the brain can learn to recruit any image regularity for the purpose of target identification. Consistent with long-term optimization for typical scene statistics, observers were better at detecting collinear contours than configurations of elements oriented at orthogonal or acute angles to the contour path. However, training resulted in improved detection of orthogonal contours that lasted for several months, suggesting retuning rather than transient changes of visual sensitivity. Improvement was also observed for acute contours but only after longer training. These results demonstrate that the brain flexibly exploits image regularities and learns to use discontinuities typically associated with surface boundaries (orthogonal, acute alignments) for contour linking and target identification. Thus, short-term experience in adulthood shapes the interpretation of scenes by assigning new statistical utility to image regularities.     

Eye gaze is not coded by cardinal mechanisms alone

Gaze is an important social cue in regulating human and non-human interactions. In this study, we employed an adaptation paradigm to examine the mechanisms underlying the perception of another''s gaze. Previous research has shown that the interleaved presentation of leftwards and rightwards gazing adaptor stimuli results in observers judging a wider range of gaze deviations as being direct. We applied a similar paradigm to examine how human observers encode oblique (e.g. upwards and to the left) directions of gaze. We presented observers with interleaved gaze adaptors and examined whether adaptation differed between congruent (adaptor and test along same axis) and incongruent conditions. We find greater adaptation in congruent conditions along cardinal (horizontal and vertical) and non-cardinal (oblique) directions suggesting gaze is not coded alone by cardinal mechanisms. Our results suggest that the functional aspects of gaze processing might parallel that of basic visual features such as orientation.     

Distractor-target interactions during directed visual attention

The spatial extent of directed visual attention (DVA) was examined in a series of experiments using precuing in a suprathreshold luminance detection (reaction time) paradigm. Previous findings (Hughes, H. C. and Zimba, L. D. J. Exp. Psychol.; Human Percept Perf., 1985, 11, 409-430) indicated that, in an empty visual field, the effects of DVA were primarily manifest as a uniform elevation of response times to all probe targets in the hemifield contralateral to the observer's expectancy. The present experiments were designed to determine whether increased spatial selectivity could be found when luminous markers indicated the exact location of the expected visual target. To maintain equivalent states of adaptation in both hemifields, luminous markers were also present at the same location in the contralateral hemifield. In general, hemifield effects were again obtained, but with two notable exceptions. First, marking locations in the unattended hemifield produced a local increase (enhanced interference) in RTs above the level characteristic of other locations within that hemifield. Second, when multiple locations were indicated with identical luminous markers, graded costs were obtained in both hemifields. However, scaling the markers according to estimates of cortical magnification factor (M) substantially reduced the slope of these inhibitory gradients, and the results once again approached those characteristic of an unstructured visual field. The findings suggest that when attention is directed to a marked location along the horizontal meridian, a transition in performance typically occurs at the vertical meridian. In addition, irrelevant stimuli some distance from the attentional focus interfere with detection times to unexpected targets that appear in the same vicinity. This interference may relate to an enhanced susceptibility to spatial interactions between the distractors and target away from the attentional focus. The interference appears to extend over a constant area of visual cortex, since it is reduced when the markers are M-scaled.     

Asymmetries in oriented-line detection indicate two orthogonal filters in early vision.

Visual detection of a line target differing in orientation from a background of lines may be achieved speedily and effortlessly. Such performance is assumed to occur early in vision and to involve filter mechanisms acting in parallel over the visual field. This study establishes orientational limits on this performance and analytically derives some generic properties of the underlying filters. It was found that, in brief displays, target orientation detection thresholds increased approximately linearly with background orientation, from minima at 0 degree (vertical) and 90 degrees, whereas background orientation detection thresholds decreased approximately linearly with target orientation, from maxima at 0 degree and 90 degrees. Target and background threshold functions were exactly antisymmetric. These data are shown to indicate a model of early line processing dominated by two classes of orientation-sensitive filter with axes close to the vertical and horizontal and orientation-tuning half-widths each of approximately 30 degrees at half-height.     

The effect of contour closure on shape perception

We studied psychophysically whether 'contour closure' enhances the accuracy of shape perception. Stimulus configurations (presented on a blank background) always consisted of identical pattern elements, but the positions of the local elements were varied: the global contour shape either contained closure or not. In the first two stimulus conditions (Closure), the oriented pattern elements (Gabor patches) formed a 'closed' rectangular shape composed of either four long lines or four corners. In the third condition (No closure), the global shape was composed of the four corners, but they were outward oriented, and hence they did not form the outline of a closed contour. We measured the precision of shape perception using a discrimination task in which observers judged the aspect ratio of the outline shape i.e. whether the rectangular shape was tall or wide. We found that: (i) shape discrimination was better (more precise) for Closed contours than for Non-closed contours, i.e. the aspect ratio discrimination thresholds were lower for the Closed than Non-closed configurations. The improved performance could not be explained by differences in visibility of the local elements in the two conditions. (ii) For closed contours, shape discrimination was more precise when the local elements were aligned with the global shape, than when the local elements were orthogonal to it.     

Scototaxis and shape discrimination in the female cricket Acheta domesticus in an arena and on a compensatory treadmill

ABSTRACT. The scototactic responses of adult female Acheta domesticus L. were tested toward various shaped targets in an orientation arena and on a compensatory treadmill. In an arena, crickets oriented toward dark targets (positive scototaxis) if they had horizontal visual angles ≥30, and if the vertical dimensions of the target was ≤ its horizontal dimension. Unattractive targets did not result in negative scototaxis but caused crickets to orient randomly with no net directionality. When complex targets were composed of two or more simple rectangular targets which had been previously defined as attractive or unattractive, intermediate responses were obtained. Crickets oriented less toward complex targets than toward simple attractive targets, but oriented more than toward simple unattractive targets. The responses of a female cricket toward an attractive target can be modified by the presence of a chemical signal emitted by previously tested females. When the signal is present females are less likely to orient toward a target that would otherwise be very attractive. This effect was not as great when the females being tested were taken directly from densely populated colonies.
When running on a compensatory treadmill, female crickets exhibit scototactic tendencies similar to those displayed in the arena. When tested on the treadmill over long periods, the amount of time spent orienting toward an attractive target increased.     

Changeable cuttlefish camouflage is influenced by horizontal and vertical aspects of the visual background

Cuttlefish change their appearance rapidly for camouflage on different backgrounds. Effective camouflage for a benthic organism such as cuttlefish must deceive predators viewing from above as well as from the side, thus the choice of camouflage skin pattern is expected to account for horizontal and vertical background information. Previous experiments dealt only with the former, and here we explore some influences of background patterns oriented vertically in the visual background. Two experiments were conducted: (1) to determine whether cuttlefish cue visually on vertical background information; and (2) if a visual cue presented singly (either horizontally or vertically) is less, equally or more influential than a visual cue presented both horizontally and vertically. Combinations of uniform and checkerboard backgrounds (either on the bottom or wall) evoked disruptive coloration in all cases, implying that high-contrast, non-uniform backgrounds are responded to with priority over uniform backgrounds. However, there were differences in the expression of disruptive components if the checkerboard was presented simultaneously on the bottom and wall, or solely on the wall or the bottom. These results demonstrate that cuttlefish respond to visual background stimuli both in the horizontal and vertical plane, a finding that supports field observations of cuttlefish and octopus camouflage. Both A. Barbosa and L. Litman are first authors. An erratum to this article can be found at     

Behavioural responses to visual stimuli by the snail Littorina irrorata

The visual capabilities of gastropod molluses and most other invertebrates possessing structurally simple eyes are poorly known. We studied vision in untrained marsh periwinkles (Littorina irrorata) in the laboratory, using oriented movements toward test shapes as the response measure. This intertidal species is active when exposed at low tide, both during the day and at night, and it travels vertically on plant stems with a tidal rhythm. In detection tests, the estimated response threshold for a single vertical bar was 0.9°, while the response threshold for an equal-size horizontal bar was 2.4° or 3.7°, depending on bar position. Snails detected a 5°-wide bar in 4.3 1x of light and a 40°-wide square having about 95% reflectance (‘off-white’) on a white (100% nominal reflectance) background in 2800 1x. Discrimination tests revealed a strong preference for vertical bars over both diagonal and horizontal bars of the same width, but no preferences in several other situations. Various factors suggest that L. irrorata may see better than most other gastropods.     

Anisotropy in the chromatic channel: a horizontal-vertical effect

We compared the chromatic contrast thresholds of drifting (2Hz) red-green sine-wave gratings of horizontal, vertical, and two oblique orientations at three spatial frequencies (2, 4, 8 cpd). Luminance contrast thresholds for yellow-black gratings were also obtained. The classic oblique effect was found for high spatial frequency luminance and chromatic stimuli. For chromatic thresholds, a significant difference was found between the horizontal and vertical thresholds of all observers. One observer was retested with her head tilted 45 deg and demonstrated that the anisotropy was specific to retinal coordinates. These results give evidence for orientation selectivity in the chromatic channel which is at least partially independent of that in the luminance channel. We estimated the degree of lateral chromatic aberration in our observers' eyes and discuss the possible contribution of this aberration to the horizontal-vertical difference in the chromatic channel.     

Cue combination and the effect of horizontal disparity and perspective on stereoacuity

Relative depth judgments of vertical lines based on horizontal disparity deteriorate enormously when the lines form part of closed configurations (Westheimer, 1979). In studies showing this effect, perspective was not manipulated and thus produced inconsistency between horizontal disparity and perspective. We show that stereoacuity improves dramatically when perspective and horizontal disparity are made consistent. Observers appear to use unhelpful perspective cues in judging the relative depth of the vertical sides of rectangles in a way not incompatible with a form of cue weighting. However, 95% confidence intervals for the weights derived for cues usually exceed the a-priori [0-1] range.