Biomedical subjects

Steven C Dakin

Publications and source records attributed to Steven C Dakin.

17 recordsLinked to original sources

PubMed2006

Flank facilitation and contour integration: different sites.

Observers' ability to integrate features into extended contours, and to exploit the flanking structure to facilitate contrast detection (flank facilitation), exhibit a similar dependence on element spacing and orientation. Here, we investigate whether this reflects the operation of a common cortical mechanism by comparing performance for both tasks under monocular, binocular, dichoptic, and stereoscopic viewing conditions. Our results clearly implicate different cortical sites for flank-facilitated detection and contour integration; the former is a purely monocular phenomenon and must therefore occur at the earliest stages of cortical processing. In contrast, contour integration is a binocular process and occurs after the encoding of relative disparity, suggesting substantial extra-striate involvement. We conclude that the sites, and therefore the mechanisms, underlying these two seemingly related psychophysical phenomena are different.

Form Perception↗

PubMed2006

Dynamic properties of orientation discrimination assessed by using classification images.

Recent physiological studies indicate that the tuning properties of neurons under acute preparation in primary visual cortex can change over time. We used a psychophysical reverse correlation paradigm to examine the potential repercussions of this neuronal property for human observers' ability to discriminate the orientation of targets over time. Observers were required to identify the orientation of a Gabor target presented within dynamic white noise. Frames from the noise movies were pooled to compute dynamic classification images (CIs) associated with the observers' discrimination performance, which then were fit with a weighted difference-of-Gabor function. Best-fitting templates were temporally bandpass, tuned to more oblique orientations than the stimulus but, crucially, did not change over time. The results suggest that the template for orientation discrimination is selected within the first 50 ms of stimulus onset and that, unlike the response of single cells, there is no measurable dynamic component to either orientation or spatial frequency tuning of human orientation discrimination.

Humans↗

PubMed2006

Integration of local motion is normal in amblyopia.

We investigate the global integration of local motion direction signals in amblyopia, in a task where performance is equated between normal and amblyopic eyes at the single element level. We use an equivalent noise model to derive the parameters of internal noise and number of samples, both of which we show are normal in amblyopia for this task. This result is in apparent conflict with a previous study in amblyopes showing that global motion processing is defective in global coherence tasks [Vision Res. 43, 729 (2003)]. A similar discrepancy between the normalcy of signal integration [Vision Res. 44, 2955 (2004)] and anomalous global coherence form processing has also been reported [Vision Res. 45, 449 (2005)]. We suggest that these discrepancies for form and motion processing in amblyopia point to a selective problem in separating signal from noise in the typical global coherence task.

Adult↗

PubMed2005

An oblique effect for local motion: psychophysics and natural movie statistics.

Human perception of visual motion is thought to involve two stages--estimation of local motion (i.e., of small features) and global motion (i.e., of larger objects)--identified with cortical areas V1 and MT, respectively. We asked if poor discrimination of oblique compared to cardinal directions (the oblique effect for motion; OEM) reflects a deficit in local or in global motion processing. We used an equivalent noise (EN) paradigm--where one measures direction discrimination thresholds in the presence of directional variability--to quantify local and global limits. We report that the OEM diminishes with increasing directional variability, indicating that global motion processing (the number of local motion signals pooled) is equal across all directions and that the OEM is attributable to anisotropies in local motion processing. To investigate the origin of this effect, we measured local motion statistics from natural movies (filmed from the point of view of a walking observer). This analysis reveals that the distribution of local directional energy on the oblique directions tends to be broader, and frequently more asymmetric, than on the cardinal directions. If motion detectors are optimized to deal with our visual world then such anisotropies likely explain the local nature of the OEM.

Adult↗

PubMed2005

Spatial interference among moving targets.

Peripheral vision for static form is limited both by reduced spatial acuity and by interference among adjacent features ('crowding'). However, the visibility of acuity-corrected image motion is relatively constant across the visual field. We measured whether spatial interference among nearby moving elements is similarly invariant of retinal eccentricity and assessed if motion integration could account for any observed sensitivity loss. We report that sensitivity to the direction of motion of a central target-highly visible in isolation-was strongly impaired by four drifting flanking elements. The extent of spatial interference increased with eccentricity. Random-direction flanks and flanks whose directions formed global patterns of rotation or expansion were more disruptive than flanks forming global patterns of translation, regardless of the relative direction of the target element. Spatial interference was low-pass tuned for spatial frequency and broadly tuned for temporal frequency. We show that these results challenge the generality of models of spatial interference that are based on retinal image quality, masking, confusions between target and flanks, attentional resolution limits or (simple) "averaging" of element parameters. Instead, the results suggest that spatial interference is a consequence of the integration of meaningful image structure within large receptive fields. The underlying connectivity of this integration favours low spatial frequency structure but is broadly tuned for speed.

Fixation, Ocular↗

PubMed2005

Local and global limitations on direction integration assessed using equivalent noise analysis.

We used an equivalent noise (EN) paradigm to examine how the human visual system pools local estimates of direction across space in order to encode global direction. Observers estimated the mean direction (clockwise or counter-clockwise of vertical) of a field of moving band-pass elements whose directions were drawn from a wrapped normal distribution. By measuring discrimination thresholds for mean direction as a function of directional variance, we were able to infer both the precision of observers' representation of each element's direction (i.e., local noise) as well as how many of these estimates they were averaging (i.e., global pooling). We estimated EN for various numbers of moving elements occupying regions of various sizes. We report that both local and global limits on direction integration are determined by the number of elements present in the display (irrespective of their density or the size of region they occupy), and we go on to show how this dependence can be understood in terms of neural noise. Specifically, we use Monte Carlo simulations to show that a maximum-likelihood operator, operating on pooled directional signals from visual cortex corrupted by Poisson noise, accounts for psychophysical data across all conditions tested, as well as motion coherence thresholds (collected under similar experimental conditions). A population vector-averaging scheme (essentially a special case of ML estimation) produces similar predictions but out-performs subjects at high levels of directional variability and fails to predict motion coherence thresholds.

Discrimination, Psychological↗

PubMed2005

Integration, segregation, and binocular combination.

The human visual system can accurately judge the mean of a distribution of different orientation samples. We ask whether the site of this integration is before or after the sites of binocular combination and disparity processing. Furthermore, we are interested in whether the efficiency with which local orientation information is integrated depends on the eye of origin. Our results suggest that orientation integration occurs after binocular integration but before disparity coding. We show that the effectiveness of added orientation noise is not only less than expected on signal or noise grounds but also that it depends on the dominance of the eye to which it is presented, suggesting an interocular opponent interaction in which the dominant eye input has higher gain.

Dominance, Ocular↗

PubMed2004

Integration of orientation information in amblyopia.

A recent report suggests that amblyopes are deficient in processing local orientation at supra-threshold contrasts. To determine whether amblyopes are also poor at integrating local orientation signals, we assessed performance for an orientation integration task in which the orientations of static signals are integrated across space. Our results show that amblyopic visual systems can integrate local static oriented signals with the same level of efficiency as normal visual systems. Although internal noise was slightly elevated, there was no indication that fewer samples were used to achieve optimal performance. This finding suggests normal integration of local orientation signals in amblyopia.

Adult↗

PubMed2003

Natural image statistics mediate brightness 'filling in'.

Although the human visual system can accurately estimate the reflectance (or lightness) of surfaces under enormous variations in illumination, two equiluminant grey regions can be induced to appear quite different simply by placing a light-dark luminance transition between them. This illusion, the Craik-Cornsweet-O'Brien (CCOB) effect, has been taken as evidence for a low-level 'filling-in' mechanism subserving lightness perception. Here, we present evidence that the mechanism responsible for the CCOB effect operates not via propagation of a neural signal across space but by amplification of the low spatial frequency (SF) structure of the image. We develop a simple computational model that relies on the statistics of natural scenes actively to reconstruct the image that is most likely to have caused an observed series of responses across SF channels. This principle is tested psychophysically by deriving classification images (CIs) for subjects' discrimination of the contrast polarity of CCOB stimuli masked with noise. CIs resemble 'filled-in' stimuli; i.e. observers rely on portions of the stimuli that contain no information per se but that correspond closely to the reported perceptual completion. As predicted by the model, the filling-in process is contingent on the presence of appropriate low SF structure.

Contrast Sensitivity↗

PubMed2003

Motion detection and the coincidence of structure at high and low spatial frequencies.

We used filtered random dot kinematograms and natural images to examine how motion detection depends the relative locations of structures defined at low and high spatial frequencies. The upper displacement limit of motion (D(max)), the lower displacement limit (D(min)) and motion coherence thresholds were unaffected by the degree of spatial coincidence between high and low spatial frequency structures i.e. whether they were consistent or inconsistent with a single feature. However motion detection was possible between band-pass filtered random dot patterns whose peak frequencies were separated by up to 4 octaves. The first result implicates spatial frequency selective motion detectors that operate independently. The second result implicates a motion system that can integrate the displacements of edges defined by widely separated spatial frequencies. Both are required to account for the two results, and they appear to operate under very similar conditions.

Contrast Sensitivity↗

PubMed2003

Grouping local directional signals into moving contours.

We consider how local motion signals are combined to represent the movements of spatially extensive objects. A series of band-pass target dots, whose collective motion defined a moving contour, was positioned within a field of randomly moving noise dots. The visibility of the contours did not depend on the direction of movement relative to local contour orientation unless the contour was constrained to pass through fixation, suggesting that a previously reported advantage for collinear motion trajectories depends on the probability of detecting any of the target elements rather than the integrated contour. Contour visibility was invariant of the spatial frequency of the elements, but it did depend on the speed, number and spacing of elements defining it, as well as the angle and spatial frequency difference between adjacent elements. Local averaging of directional signals is not sufficient to explain these results. The visibility of these moving contours identifies narrow-band grouping processes that are sensitive to the shape defined by the directions of the elements forming the contour.

Humans↗

PubMed2003

The shape and size of crowding for moving targets.

Our ability to identify alphanumeric characters can be impaired by the presence of nearby features, especially when the target is presented in the peripheral visual field, a phenomenon is known as crowding. We measured the effects of motion on acuity and on the spatial extent of crowding. In line with many previous studies, acuity decreased and crowding increased with eccentricity. Acuity also decreased for moving targets, but the absolute size of crowding zones remained relatively invariant of speed at each eccentricity. The two-dimensional shape of crowding zones was measured with a single flanking element on each side of the target. Crowding zones were elongated radially about central vision, relative to tangential zones, and were also asymmetrical: a more peripheral flanking element crowded more effectively than a more foveal one; and a flanking element that moved ahead of the target crowded more effectively than one that trailed behind it. These results reveal asymmetrical space-time dependent regions of visual integration that are radially organised about central vision.

Eye Movements↗

PubMed2003

Theories of developmental dyslexia: insights from a multiple case study of dyslexic adults.

A multiple case study was conducted in order to assess three leading theories of developmental dyslexia: (i) the phonological theory, (ii) the magnocellular (auditory and visual) theory and (iii) the cerebellar theory. Sixteen dyslexic and 16 control university students were administered a full battery of psychometric, phonological, auditory, visual and cerebellar tests. Individual data reveal that all 16 dyslexics suffer from a phonological deficit, 10 from an auditory deficit, four from a motor deficit and two from a visual magnocellular deficit. Results suggest that a phonological deficit can appear in the absence of any other sensory or motor disorder, and is sufficient to cause a literacy impairment, as demonstrated by five of the dyslexics. Auditory disorders, when present, aggravate the phonological deficit, hence the literacy impairment. However, auditory deficits cannot be characterized simply as rapid auditory processing problems, as would be predicted by the magnocellular theory. Nor are they restricted to speech. Contrary to the cerebellar theory, we find little support for the notion that motor impairments, when found, have a cerebellar origin or reflect an automaticity deficit. Overall, the present data support the phonological theory of dyslexia, while acknowledging the presence of additional sensory and motor disorders in certain individuals.

Adult↗

PubMed2003

Integration of first- and second-order orientation.

The problem of how visual information such as orientation is combined across space bears on key visual abiities, such as texture perception. Orientation signals can be derived from both luminance and contrast, but it is not well understood how such information is pooled or how these different orientation signals interact in the integration process. We measured orientation discrimination thresholds for arrays of equivisible first-order and second-order Gabors. Thresholds were measured as the orientation variability in the arrays increased, and we estimated the number of samples (or efficiency) and internal noise of the mechanism being used. Observers were able to judge the mean orientation of arrays of either first- or second-order Gabors. For arrays of first-order and arrays of second-order Gabors, estimates of the number of samples used increased as the number of Gabors increased. When judging the orientation of arrays of either order, observers were able to ignore randomly oriented Gabors of the opposite order. If observers did not know which Gabor type carried the more useful orientation information, they tended to use the information from first-order Gabors (even when this was poorer information). Observers were unable to combine information from first- and second-order Gabors, though this would have improved their performance. The visual system appears to have separate integrators for combining local orientation across space for luminance- and contrast-defined features.

Discrimination, Psychological↗

PubMed2002

Comparison of the spatial-frequency selectivity of local and global motion detectors.

Convergent physiological and behavioral evidence indicates that the initial receptive fields responsible for motion detection are spatially localized. Consequently, the perception of global patterns of movement (such as expansion) requires that the output of these local mechanisms be integrated across visual space. We have differentiated local and global motion processes, with mixtures of coherent and incoherent moving patterns composed of bandpass filtered dots, and have measured their spatial-frequency selectivity. We report that local motion detectors show narrow-band spatial-frequency tuning (i.e., they respond only to a narrow range of spatial frequencies) but that global motion detectors show broadband spatial-frequency tuning (i.e., they integrate across a broad range of spatial frequencies), with a preference for low spatial frequencies.

Humans↗

PubMed2002

Role of synchrony in contour binding: some transient doubts sustained.

The temporal correlation hypothesis proposes that neurons signal mutual inclusion in complex features, such as extended contours, by phase-locking their firing [C. M. Gray and W. Singer, Proc. Nat]. Acad. Sci. USA 86, 1698 (1989)]. Although this hypothesis remains controversial, a number of recent psychophysical studies have suggested that temporal correlation among features can indeed promote perceptual grouping. In particular, subjects are better at detecting extended visual contours embedded within a field of distractor elements when a small delay is present between a cycling presentation of the contour and the background [Nature 394, 179 (1988)]. We have replicated this finding and examined three potentially confounding factors. First, we controlled local density and used more curved contours composed of bandpass elements to confirm that the effect was associated with contour integration and not with the operation of coarse-scale spatial filters. Second, we minimized the effects of saccadic eye movements (which could combine with the flicker of the asynchronous display to introduce motion cues at the contour location) both by using a fixation marker that was visible only when observers made a saccade (allowing them to reject these trials) and by retinally stabilizing the stimulus. We report that eye movements contribute to the effect. Third, we asked if either visible persistence or transients at the onset and the offset of the asynchronous stimuli might contribute to the effect. We report that the effect is largely abolished by the inclusion of prestimulus and poststimulus masks and is entirely abolished by ramping the contrast of the stimulus on and off. Neither ramping, masking, nor stabilization should specifically disrupt a contour-binding scheme based on temporal synchrony, and we conclude that it is the transient component at the onset and the offset of these stimuli that is responsible for the reported advantage for asynchronous presentation.

Contrast Sensitivity↗

PubMedDate not supplied

Critical band masking in optic flow.

Visual processing has been widely investigated with narrow band stimuli at low contrasts. We used a masking paradigm to examine how visual sensitivity under these conditions compares with the perception of the direction of heading in real scenes (i.e., with dynamic natural images at high contrasts). We first confirmed and extended previous studies showing biases in the amplitude distribution for spatial frequency, temporal frequency, speed and direction in dynamic natural movies. We then measured contrast thresholds for identification of the direction of motion for an observer traveling at various speeds. In spite of differences in contrast sensitivity and large non-uniformities in the amplitude content of the stimuli, contrast thresholds were relatively invariant of spatial frequency and completely invariant of temporal frequency, speed and direction. Our results suggest that visual processing normalises responses to supra-threshold structure at different spatial and temporal frequencies within natural stimuli and so equates their effective visibility.

Contrast Sensitivity↗