Paul B. Hibbard

Visual Processing and Dyslexia

Magnocellular-pathway deficits have been hypothesised to be responsible for the problems experienced by dyslexic individuals in reading. However, research has yet to provide a detailed account of the consequences of these deficits or to identify the behavioural link between them and reading disabilities. The aim of the present study was to determine the potential consequences of the magnocellular-pathway deficits for dyslexics in a comprehensive range of visual tasks. Dyslexics and nondyslexics were compared on their ability to (i) perform vernier-acuity and orientation-acuity tasks; (ii) perceive motion by using a range of measures common in the psychophysical literature (Dmin, Dmax, and global coherence); and (iii) perceive shapes presented in random-dot stereograms at a range of disparity pedestals, thereby dissociating stereopsis from vergence control. The results indicated no significant differences in performance between the dyslexic and nondyslexic subjects in terms of the visual-acuity measures. In general, dyslexics performed relatively poorly on measures of motion perception and stereopsis, although when considered individually some of the dyslexics performed better than some of the controls. The poor performance of the dyslexics in the stereogram tasks was attributable to a subgroup of dyslexics who also appeared to have severe difficulty with the motion-coherence task. These data are consistent with previous evidence that some dyslexics may have deficits within the magnocellular visual pathway.

Spatial frequency and visual discomfort

Images created from noise filtered to have an approximately 1/f amplitude spectrum were altered by adding excess energy concentrated at various spatial frequencies. The effects of this manipulation on judgements of visual discomfort were studied. Visual noise with a 1/f amplitude spectrum (typical of natural images) was judged more comfortable than any image with a relative increase in contrast energy within a narrow spatial frequency band. A peak centred on 0.375-1.5cycles/degree of spatial frequency was consistently judged as more uncomfortable than a peak at a higher spatial frequency. This finding was robust to slight differences in eccentricity, and when stimuli were matched for perceived contrast across spatial frequency. These findings are consistent with the idea that deviation from the statistics of natural images could cause discomfort because the visual system is optimised to encode images with the particular statistics typical of natural scenes.

Reaching for virtual objects: binocular disparity and the control of prehension.

Abstract. Although, in principle, binocular cues provide veridical information about the three-dimensional shape of objects, our perception on the basis of these cues is distorted systematically. The consequences of these distortions may be less serious than they first appear, however, since in everyday life we rarely are required to judge the absolute shape, size or distance of objects. An important exception to this is in the control of prehension, where veridical information about an object to be grasped is required to plan the transport of the hand and to select the most appropriate grip. Here we investigate whether binocular cues provide accurate depth information for the control of prehension using disparity-defined, virtual objects and report that whilst binocular disparity can support prehensile movements, the kinematic indices, which reflect distance-reached and perceived size, show clear biases. These results suggest that accurate metric depth information for the control of prehension is not available from binocular cues in isolation.

Seeing in 3-D With Just One Eye Stereopsis Without Binocular Vision

Humans can perceive depth when viewing with one eye, and even when viewing a two-dimensional picture of a three-dimensional scene. However, viewing a real scene with both eyes produces a more compelling three-dimensional experience of immersive space and tangible solid objects. A widely held belief is that this qualitative visual phenomenon (stereopsis) is a by-product of binocular vision. In the research reported here, we empirically established, for the first time, the qualitative characteristics associated with stereopsis to show that they can occur for static two-dimensional pictures without binocular vision. Critically, we show that stereopsis is a measurable qualitative attribute and that its induction while viewing pictures is not consistent with standard explanations based on depth-cue conflict or the perception of greater depth magnitude. These results challenge the conventional understanding of the underlying cause, variation, and functional role of stereopsis.

Linear filtering precedes nonlinear processing in early vision

BACKGROUND Nonlinearities play a significant role in early visual processing. They are central to the perception of spatial contrast variations, multiplicative transparencies and texture boundaries. This article concerns the stage of processing at which nonlinearities first become significant. RESULTS Subjects were adapted to a high contrast sinusoidal grating followed by a brief presentation of a contrast modulated test (plaid) pattern. Thresholds for the detection of the contrast modulation (the beat) were measured. Results show that threshold elevation is greatest when the orientation and spatial frequency of the adapting grating are close to the principal Fourier frequency (the carrier) of the test pattern. Adaptation to sinewave-gratings near the frequency of the contrast modulation has relatively little effect. The data also show that the processing of contrast is frequency selective, with a peak tuning frequency near 0.4 cycles per degree. CONCLUSIONS The data are consistent with a model in which the contrast beats are processed in a frequency-specific manner, after an initial stage of frequency-specific and orientation-specific linear filtering.

Does binocular disparity facilitate the detection of transparent motion

Recent physiological studies have established that cortical cells that are tuned for the direction of motion may also exhibit tuning for binocular disparity. This tuning does not appear to provide any advantage in discriminating the direction of global motion in random-dot kinematograms. Here we investigated the possibility that this tuning may be important in the perception of transparent motion. Random-dot kinematograms were presented which contained coherent motion in a single direction or in two opposing directions. A greater proportion of signal dots was required for the detection of transparent motion than of motion in a single direction. This difference vanished when the two opposite directions of motion were presented with different disparities. These results suggest that the direction of global motion can be computed separately for surfaces which are clearly segregated in depth.

Binocular energy responses to natural images.

The binocular energy model provides a good description of the first stages of cortical binocular processing. Three important determinants of the responses of neurons under this model are the disparity of a stimulus, its spatial variation in disparity and its second-order luminance statistics. The influence of the latter two factors on the disparity tuning of the energy model were investigated. While each can have a significant effect on the energy response, neither presents a significant challenge when one considers the range of variation expected in natural images. The response of the energy model to natural binocular images was also investigated. The strongest responses were found for model neurons tuned to small disparities. This trend was more evident for vertical than for horizontal disparity, and flattened rapidly as image eccentricity increased. These results are predicted on the basis of simple geometrical considerations, and are reflected in both physiological and psychophysical measures of the disparity tuning of the visual system.

A statistical model of binocular disparity

Binocular disparity provides important information about the three-dimensional structure of the environment. The current study sought to complement our geometrical understanding of binocular vision by considering the distributions of horizontal and vertical disparities that might be expected in images of the natural environment, using a simple environmental model. It was observed that the distribution of disparities depends critically on fixation, and varies greatly from one image location to another. The results were considered in relation to computational models of binocular stereopsis, and compared to two known properties of the visual system—the small disparity preference in disparity matching, and the influence of eccentricity on Panums fusional limit. Overall, the study characterizes the binocular disparities that are likely to be encountered in the real world scenes, and discusses the implications of these for our understanding of binocular visual systems.

Stereopsis from contrast envelopes

We report two experiments concerning the site of the principal nonlinearity in second-order stereopsis. The first exploits the asymmetry in perceiving transparency with second-order stimuli found by Langley et al. (1998) (Proceedings of the Royal Society of London B, 265, 1837-1845) i.e. the product of a positive-valued contrast envelope and a mean-zero carrier grating can be seen transparently only when the disparities are consistent with the envelope appearing in front of the carrier. We measured the energy at the envelope frequencies that must be added in order to negate this asymmetry. We report that this amplitude can be predicted from the envelope sidebands and not from the magnitude of compressive pre-cortical nonlinearities measured by other researchers. In the second experiment, contrast threshold elevations were measured for the discrimination of envelope disparities following adaptation to sinusoidal gratings. It is reported that perception of the envelopes depth was affected most when the adapting grating was similar (in orientation and frequency) to the carrier, rather than to the contrast envelope. These results suggest that the principal nonlinearity in second-order stereopsis is cortical, occurring after orientation- and frequency-selective linear filtering.

Statistically optimal integration of biased sensory estimates.

Experimental investigations of cue combination typically assume that individual cues provide noisy but unbiased sensory information about world properties. However, in numerous instances, including real-world settings, observers systematically misestimate properties of the world from sensory information. Two such instances are the estimation of shape from stereo and motion cues. Bias in single-cue estimates, therefore poses a problem for cue combination if the visual system is to maintain accuracy with respect to the world, particularly because knowledge about the magnitude of bias in individual cues is typically unknown. Here, we show that observers fail to take account of the magnitude of bias in each cue during combination and instead combine cues in proportion to their reliability so as to increase the precision of the combined-cue estimate. This suggests that observers were unaware of the bias in their sensory estimates. Our analysis of cue combination shows that there is a definable range of circumstances in which combining information from biased cues, rather than vetoing one or other cue, can still be beneficial, by reducing error in the final estimate.