Charles A. Heywood

Attention without awareness in blindsight

The act of attending has frequently been equated with visual awareness. We examined this relationship in ‘blindsight’: a condition in which the latter is absent or diminished as a result of damage to the primary visual cortex. Spatially selective visual attention is demonstrated when information that stimuli are likely to appear at a specific location enhances the speed or accuracy of detection of stimuli subsequently presented at that location. In a blindsight subject, we showed that attention can confer an advantage in processing stimuli presented at an attended location, without those stimuli entering consciousness. Attention could be directed both by symbolic cues in the subjects spared field of vision or cues presented in his blind field. Cues in his blind field were even effective in directing his attention to a second location remote from that at which the cue was presented. These indirect cues were effective whether or not they themselves elicited non–visual awareness. We concluded that the spatial selection of information by an attentional mechanism and its entry into conscious experience cannot be one and the same process.

Attended but unseen: Visual attention is not sufficient for visual awareness

Does any one psychological process give rise to visual awareness? One candidate is selective attention-when we attend to something it seems we always see it. But if attention can selectively enhance our response to an unseen stimulus then attention cannot be a sufficient precondition for awareness. Kentridge, Heywood & Weiskrantz [Kentridge, R. W., Heywood, C. A., & Weiskrantz, L. (1999). Attention without awareness in blindsight. Proceedings of the Royal Society of London, Series B, 266, 1805-1811; Kentridge, R. W., Heywood, C. A., & Weiskrantz, L. (2004). Spatial attention speeds discrimination without awareness in blindsight. Neuropsychologia, 42, 831-835.] demonstrated just such a dissociation in the blindsight subject GY. Here, we test whether the dissociation generalizes to the normal population. We presented observers with pairs of coloured discs, each masked by the subsequent presentation of a coloured annulus. The discs acted as primes, speeding discrimination of the colour of the annulus when they matched in colour and slowing it when they differed. We show that the location of attention modulated the size of this priming effect. However, the primes were rendered invisible by metacontrast-masking and remained unseen despite being attended. Visual attention could therefore facilitate processing of an invisible target and cannot, therefore, be a sufficient precondition for visual awareness.

Separate Channels for Processing Form, Texture, and Color: Evidence from fMRI Adaptation and Visual Object Agnosia

Previous neuroimaging research suggests that although object shape is analyzed in the lateral occipital cortex, surface properties of objects, such as color and texture, are dealt with in more medial areas, close to the collateral sulcus (CoS). The present study sought to determine whether there is a single medial region concerned with surface properties in general or whether instead there are multiple foci independently extracting different surface properties. We used stimuli varying in their shape, texture, or color, and tested healthy participants and 2 object-agnosic patients, in both a discrimination task and a functional MR adaptation paradigm. We found a double dissociation between medial and lateral occipitotemporal cortices in processing surface (texture or color) versus geometric (shape) properties, respectively. In Experiment 2, we found that the medial occipitotemporal cortex houses separate foci for color (within anterior CoS and lingual gyrus) and texture (caudally within posterior CoS). In addition, we found that areas selective for shape, texture, and color individually were quite distinct from those that respond to all of these features together (shape and texture and color). These latter areas appear to correspond to those associated with the perception of complex stimuli such as faces and places.

Separate Processing of Texture and Form in the Ventral Stream: Evidence from fMRI and Visual Agnosia

Real-life visual object recognition requires the processing of more than just geometric (shape, size, and orientation) properties. Surface properties such as color and texture are equally important, particularly for providing information about the material properties of objects. Recent neuroimaging research suggests that geometric and surface properties are dealt with separately within the lateral occipital cortex (LOC) and the collateral sulcus (CoS), respectively. Here we compared objects that differed either in aspect ratio or in surface texture only, keeping all other visual properties constant. Results on brain-intact participants confirmed that surface texture activates an area in the posterior CoS, quite distinct from the area activated by shape within LOC. We also tested 2 patients with visual object agnosia, one of whom (DF) performed well on the texture task but at chance on the shape task, whereas the other (MS) showed the converse pattern. This behavioral double dissociation was matched by a parallel neuroimaging dissociation, with activation in CoS but not LOC in patient DF and activation in LOC but not CoS in patient MS. These data provide presumptive evidence that the areas respectively activated by shape and texture play a causally necessary role in the perceptual discrimination of these features.

Visual Salience in the Change Detection Paradigm: The Special Role of Object Onset.

The relative efficacy with which appearance of a new object orients visual attention was investigated. At issue is whether the visual system treats onset as being of particular importance or only 1 of a number of stimulus events equally likely to summon attention. Using the 1-shot change detection paradigm, the authors compared detectability of new objects with changes occurring at already present objects--luminance change, color change, and object offset. Results showed that appearance of a new object was less susceptible to change blindness than changes that old objects could undergo. The authors also investigated whether it is onset per se that leads to enhanced detectability or onset of an object representation. Results showed that the onset advantage was eliminated for onsets that did not correspond with the appearance of a new object. These findings suggest that the visual system is particularly sensitive to the onset of a new object.

Infants’ visual preference for sex-congruent babies, children, toys and activities: A longitudinal study

Sex differences in social behaviour emerge as early as 2 years of age and gender schema theorists have suggested that preverbal infants possess ‘tacit’ knowledge of gender which informs their behaviour. This study examined sex-congruent preferences using a visual preference paradigm in four domains (babies, children, toys, activities) in a longitudinal study of infants aged 3, 9 and 18 months. At 3 months, infants showed a marginally significant preference for same-sex babies driven principally by males. Sex-congruent toy preference was found among males at ages 9 and 18 months. Both sexes preferred masculine activity styles but this effect was significantly stronger among males than females. Gender schema theory requires gendered self-concept as a precursor to sex-congruent preference. Infants did not recognize themselves from photographs at any of the ages tested. By 18 months approximately two thirds of infants showed self-recognition on the rouge test. However, at none of the ages and in none of the domains tested was self-recognition related to sex-congruent preference. Cross-domain consistency of preference was not found. There was evidence of some stability of preference within domains between the ages of 9 and 18 months and this stability was very marked for activity preference.

The Significance of Visual Information Processing in Reading: Insights from Hemianopic Dyslexia.

We present the first comprehensive review of research into hemianopic dyslexia since Mauthners original description of 1881. We offer an explanation of the reading impairment in patients with unilateral homonymous visual field disorders and clarify its functional and anatomical bases. The major focus of our review is on visual information processing, visuospatial attention and eye-movement control during reading. An advanced understanding of the basis of hemianopic dyslexia and its rehabilitation also increases our knowledge about normal reading and its underlying neural mechanisms. By drawing together various sources of evidence we illustrate the significance of bottom-up and attentional top-down control of visual information processing and saccadic eye-movements in reading. Reading depends critically on the cortical-subcortical network subserving the integration of visual, attentional and oculomotor processes involved in text processing.

Detectability of onsets versus offsets in the change detection paradigm.

The human visual system is particularly sensitive to abrupt onset of new objects that appear in the visual field. Onsets have been shown to capture attention even when other transients simultaneously occur. This has led some authors to argue for the special role that object onset plays in attentional capture. However, evidence from the change detection paradigm appears contradictory to such findings. Studies of change blindness demonstrate that the onset of new objects can often go unnoticed. Assessing the relative detectability of onsets compared with other visual transients in a change detection procedure may help resolve this contradiction. We report the results of four experiments investigating the efficacy with which onsets capture attention compared with offsets. In Experiment 1, we employed a standard flicker procedure and assessed whether participants were more likely to detect the change following a frame containing an onset or following a frame containing an offset. In Experiment 2, we employed the one-shot method and investigated whether participants detected more onsets or offsets. Experiment 3 used the same method but assessed whether onsets would be detected more rapidly than offsets. In Experiment 4, we investigated whether the effect obtained in Experiments 1-3 using simple shapes would replicate when images of real-world objects were used. Results showed that onsets were less susceptible to change blindness than were offsets. We argue that the preservation of information is greater in onsets than in offsets.

Residual vision in multiple retinal locations within a scotoma: Implications for blindsight

There is an important new proposal that blindsight-the ability to detect and identify visual stimuli by forcedchoice guessing and in the absence of conscious awareness when they fall in blind regions of the visual fieldis a function of residual islands of undamaged visual cortex. This stands in contrast to the widely accepted view that blindsight is exclusively a function of secondary visual pathways. According to the new view, residual vision in blindsight should be patchy. Thus, when apparently wide areas of residual vision in blindsight are found, these may be due to eye-movements that allow stimuli to pass over retinal locations corresponding to islands of sparing. We tested this hypothesis by examining the distribution of residual vision in blindsight when the effects of eye movements on the retinal location of stimuli were minimized. We report a series of experiments that examined twealternate forcedchoice discrimination in the blind field of the subject GY. Using a dual-Purkinje image eye-tracker we applied three methods of minimizing the effects of retinal slippage due to eye-movements on discrimination performance: fixation stability-dependent trials, software image stabilization, and post hoc rejection of trials in which saccadic eye-movements were detected. In the first experiment, GYs discrimination performance was significantly above chance in 8 of 15 locations tested. In the subsequent experiments the subject knew the location of the target in each block of trials, and this resulted in improvements to performance in a further three locations. Increasing the luminance of the stimulus display (while maintaining 95% target contrast), and increasing the temporal discriminability of the forced choice produced performance above chance in all but two of the locations tested. The consistent chance performance observed in two locations in the lower visual field nevertheless implies that GYs blindsight does not extend over the whole of his scotoma. Nevertheless, abolishing, or minimizing, the effects of eye-movements did not result in a loss of detection in all the widely separated regions tested, and we thus conclude that GYs blindsight cannot adequately be explained in terms of islands of spared vision. Islands may account for residual vision in scotomata in some patients, but cannot be a universal account of the phenomenon of blindsight.

Effects of temporal cueing on residual visual discrimination in blindsight.

We tested the ability of a blindsight patient, GY, to identify in which of two locations a target was presented in a spatial two-alternative forced choice paradigm (spatial 2AFC). On each trial the subject was asked to make a second manual response indicating whether he had had any awareness of an event occurring during the trial. A cue, presented at the fixation location, could signal the 0.4 s period over which the target appeared within the 10 s duration of each trial. Targets of three contrasts, 93, 43 and 22% were used. We found that GYs ability to discriminate the location of targets in his blind field remained significantly above chance, with and without cueing, for each contrast. Cueing, did, however, significantly improve his performance for low contrast targets. When he performed a similar task with near threshold contrast targets in his spared visual field his discrimination was at chance unless the presentation of targets was cued, despite his reporting more awareness for these stimuli than he did for low-contrast stimuli in his blind field. These results are compared with those previously reported in monkeys who received lesions to their visual cortices as infants or adults. We conclude that (1) GYs blindsight is qualitatively different from near-threshold normal vision. (2) In common with infant-lesioned monkeys his blindsight remains even in the absence of temporal cues. (3) Residual vision is subject to modulation by attentional processes, or arousal, associated with temporal cueing.