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Biomedical subjects

A Cowey

Publications and source records attributed to A Cowey.

At least 55 records · Page 3Linked to original sources
PubMed1999

Differential pupillary constriction and awareness in the absence of striate cortex.

The fact that the pupil constricts differentially to visual stimuli in the absence of changes in light energy makes it a valuable tool for studying normal function as well as residual capacity in hemianopic subjects. When pupillometrically effective stimuli such as equiluminant gratings or coloured patches with an abrupt onset and offset are presented to the 'blind' hemifield, a hemianopic subject with damage largely restricted to striate cortex (V1) sometimes reports being 'aware' of the transient onset/offset, although without 'seeing' as such. The question addressed here is whether the pupil still responds in the condition of blindsight in its strict sense--i.e. discriminative capacity in the absence of acknowledged awareness--when stimuli are deliberately designed to eliminate awareness. This was accomplished by making stimulus onset and offset slow and gradual. The results with a well-studied hemianope, G.Y., demonstrate that there is still a pupillary constriction to isoluminant achromatic gratings and red-coloured stimuli, although reduced in size, in the absence of acknowledged awareness.

Accidents, Traffic↗
PubMed1999

Perception of first- and second-order motion: separable neurological mechanisms?

An unresolved issue in visual motion perception is how distinct are the processes underlying "first-order" and "second-order" motion. The former is defined by spatiotemporal variations of luminance and the latter by spatiotemporal variations in other image attributes, such as contrast or depth. Here we describe two neurological patients with focal unilateral lesions whose contrasting perceptual deficits on psychophysical tasks of "first-order" and "second-order" motion are related to the maps of the human brain established by functional neuroimaging and gross anatomical features. We used a relatively fine-grained neocortical parcellation method applied to high-resolution MRI scans of the patients' brains to illustrate a subtle, yet highly specific dissociation in the visual motion system in humans. Our results suggest that the two motion systems are mediated by regionally separate mechanisms from an early stage of cortical processing.

Adult↗
PubMed1998

Task-specific impairments and enhancements induced by magnetic stimulation of human visual area V5.

Transcranial magnetic stimulation (TMS) can be used to simulate the effects of highly circumscribed brain damage permanently present in some neuropsychological patients, by reversibly disrupting the normal functioning of the cortical area to which it is applied. By using TMS we attempted to recreate deficits similar to those reported in a motion-blind patient and to assess the specificity of deficits when TMS is applied over human area V5. We used six visual search tasks and showed that subjects were impaired in a motion but not a form 'pop-out' task when TMS was applied over V5. When motion was present, but irrelevant, or when attention to colour and form were required, TMS applied to V5 enhanced performance. When attention to motion was required in a motion-form conjunction search task, irrespective of whether the target was moving or stationary, TMS disrupted performance. These data suggest that attention to different visual attributes involves mutual inhibition between different extrastriate visual areas.

Adult↗
PubMed1998

Visual form discrimination from texture cues: a PET study.

With the purpose of localising the cerebral cortical areas participating in the discrimination of visual form generated exclusively by texture cues, we measured changes in regional cerebral blood flow (rCBF) with positron emissions tomography (PET) and 15O-butanol as the tracer. The subjects performed two odd-one-out discrimination tasks: a form-from-texture discrimination task (in which a visual form was defined by differences in texture) and its reference task, the discrimination of texture. During task performance, activated fields were present bilaterally in the primary visual cortex and its immediate extrastriate cortex, the right lateral occipital gyrus, bilaterally in the fusiform and superior temporal gyri and posterior parts of the superior parietal lobules, along the medial bank of the right intraparietal sulcus, and in the right supramarginal gyrus. Other fields were found in the cingulate and prefrontal cortex. The findings demonstrate that the discrimination of visual form as defined by texture engages cortical fields that are widely distributed ion the human brain. In the visual cortex, the activated fields are present in both the occipito-temporal and occipito-parietal visual areas. These results suggest that the perception and discrimination of forms in the visual system requires the joint-activation of neuronal populations in the visual cortex.

Adult↗
PubMed1998

Blindsight and visual awareness.

Some patients with damaged striate cortex have blindsight-the ability to discriminate unseen stimuli in their clinically blind visual field defects when forced-choice procedures are used. Blindsight implies a sharp dissociation between visual performance and visual awareness, but signal detection theory indicates that it might be indistinguishable from the behavior of normal subjects near the lower limit of conscious vision, where the dissociations could arise trivially from using different response criteria during clinical and forced-choice tests. We tested the latter possibility with a hemianopic subject during yes-no and forced-choice detection of static and moving targets. His response criterion differed significantly between yes-no and forced-choice responding, and the difference was sufficient to produce a blindsight-like dissociation with bias-sensitive measures of performance. When measured independently of bias, his sensitivity to static targets was greater in the forced-choice than in the yes-no task (unlike normal control subjects), but his sensitivity to moving targets did not differ. Differences in response criterion could therefore account for dissociations between yes-no and forced-choice detection of motion, but not of static pattern. The results explain why patients with blindsight are apparently more often "aware" of moving stimuli than of static stimuli. However, they also imply that blindsight is unlike normal vision near threshold, and that pattern- and motion-detection in blindsight may depend on different sets of neural mechanisms during yes-no and forced-choice tests.

Adult↗
PubMed1998

Effects of unseen stimuli on reaction times to seen stimuli in monkeys with blindsight.

In three macaque monkeys with unilateral removal of primary visual cortex and in one unoperated monkey, we measured reaction times to a visual target that was presented at a lateral eccentricity of 20 degrees in the normal, left, visual hemifield. When an additional stimulus was presented at the corresponding position in the right hemifield (hemianopic in three of the monkeys), it significantly slowed the reaction time to the left target if it preceded it by delays from 100-500 msec. The most effective delay depended on the particular experimental paradigm and perhaps on the experience of the monkey with the task. The results show that reaction times to seen targets in the normal hemifield of monkeys are influenced by the presentation of "unseen" targets in the anopic hemifield, as in some patients with cortically blind visual field defects.

Animals↗
PubMed1998

Cortical color blindness is not "blindsight for color".

Cortical color blindness, or cerebral achromatopsia, has been likened by some authors to "blindsight" for color or an instance of "covert" processing of color. Recently, it has been shown that, although such patients are unable to identify or discriminate hue differences, they nevertheless show a striking ability to process wavelength differences, which can result in preserved sensitivity to chromatic contrast and motion in equiluminant displays. Moreover, visually evoked cortical potentials can still be elicited in response to chromatic stimuli. We suggest that these demonstrations reveal intact residual processes rather than the operation of covert processes, where proficient performance is accompanied by a denial of phenomenal awareness. We sought evidence for such covert processes by conducting appropriate tests on achromatopsic subject M.S. An "indirect" test entailing measurement of reaction times for letter identification failed to reveal covert color processes. In contrast, in a forced choice oddity task for color, M.S. was unable to verbally indicate the position of the different color, but was surprisingly adept at making an appropriate eye movement to its location. This "direct" test thus revealed the possible covert use of chromatic differences.

Blindness, Cortical↗
PubMed1998

The effect of lesions to cortical areas V4 or AIT on pupillary responses to chromatic and achromatic stimuli in monkeys.

We measured the pupillary response to achromatic and chromatic grating stimuli in left and right visual hemifields of two rhesus monkeys, who were trained to fixate the centre of a screen. After removing the rostral inferior temporal cortex of one hemisphere, the response to chromatically modulated gratings in the contralateral hemifield was abolished, whereas the response to the luminance modulated grating was unaffected. In one of the monkeys, in which area V4 of the other hemisphere was also removed, there was no effect on the pupillary response to either kind of grating presented in the hemifield contralateral to the V4 lesion. The results show that the cortical contribution to the response of the pupil to purely chromatic changes is mediated by rostral temporal cortex, not by area V4.

Animals↗
PubMed1998

Discrimination of cone contrast changes as evidence for colour constancy in cerebral achromatopsia.

One proposed mechanism for underpinning colour constancy is computation of the relative activity of cones within one class--cone ratios, or cone contrasts--between surfaces in a fixed scene undergoing a change in illuminant. Although there is evidence that cone ratios do determine colour appearance under many conditions, the site or sites of their computation is unknown. Here, we report that a cerebrally achromatopsic observer, MS, displayed evidence of colour constancy in asymmetric colour matching tasks and was able to discriminate changes in cone ratios for simple, but not complex scenes. We hypothesise that the site of local cone-ratio computation is therefore early in the visual system, probably retinal.

Color Perception↗
PubMed1998

Form and motion from colour in cerebral achromatopsia.

Patients with cerebral achromatopsia, resulting from damage to ventromedial occipital cortex, cannot chromatically order, or discriminate, hue. Nevertheless, their chromatic contrast sensitivity can be indistinguishable from that of normal observers. A possible contributor to the detectability of chromatic gratings is the subadditive nature of certain colour combination such that mixtures of, for example, red and green (yielding yellow) appear dimmer than expected from the simple addition of luminances. This subadditivity is believed to reflect colour-opponent interactions between the outputs of long- and medium-wavelength cones. We performed a first-order compensation for such subadditivity in chromatic gratings and demonstrated that their detection was still not abolished in an achromatopsic patient. In addition, we used a two-alternative forced-choice procedure with an achromatopsic patient, who was required to judge the apparent relative velocity of two drifting gratings with different degrees of compensation for subadditivity. It is well known that isoluminant gratings, constructed by adding a red and green sinusoidal grating of identical peak luminances in antiphase, appear to drift substantially slower than an achromatic grating with the same velocity. Adding 2f luminance compensation to an isoluminant grating of spatial frequency f, resulted in an identical minimum of perceived velocity at a compensation contrast of 5% in both achromatopsics and normal observers. Furthermore, while compensation for subadditivity did not substantially compromise grating detection at low contrasts, such correction severely affected motion detection. Saccadic eye movement accuracy and latency were also measured to uncompensated chromatic, compensated chromatic and achromatic targets. We conclude first that subadditivity, resulting from colour-opponent P-channel processes, influences motion judgements. The ability to extract motion from chromatic differences alone is little, if at all, different in achromatopsic and normal vision. Second, the paradoxical detection of sinusoidally modulated chromatic gratings in achromatopsic patients is not merely a result of subadditivity. Third, saccadic latency, but not accuracy, to chromatic targets is affected by luminance compensation. Finally, and more generally, wavelength processing continues to contribute to several aspects of visual processing even when colour is not perceived.

Adult↗
PubMed1998

Colour constancy impairments in patients with lesions of the prestriate cortex.

Colour matching and colour constancy were studied in seven patients and 46 control subjects. Subjects were required to match Munsell Colour Chips presented under either identical or different illumination. Three of the patients had deficits in colour constancy, i.e. failure to compensate for the change in the wavelength composition of the illumination. Two of the patients with defective constancy had suffered bilateral cortical damage to the posterior lingual and fusiform gyri, and one patient had a lesion restricted to the same regions of the right hemisphere. Our observations indicate that these cortical areas, which include part of putative human area V4, play an important role in colour constancy.

Adult↗
PubMed1998

Cortical plasticity in perceptual learning demonstrated by transcranial magnetic stimulation.

Performance on a wide range of perceptual tasks improves with practice. Most accounts of perceptual learning are concerned with changes in neuronal sensitivity or changes in the way a stimulus is represented. Another possibility is that different areas of the brain are involved in performing a task during and after learning it. Here, we demonstrate that the right parietal cortex is involved in novel but not learned visual conjunction search. We observed that single pulse transcranial magnetic stimulation (TMS) to the right parietal cortex impairs visual conjunction search when the stimuli are novel and require a serial search strategy, but not once the particular search task has been learned. The effect of TMS returns when a different, novel, serial search task is presented.

Electric Stimulation↗
PubMed1998

Cortical plasticity in perceptual learning demonstrated by transcranial magnetic stimulation.

Performance on a wide range of perceptual tasks improves with practice. Most accounts of perceptual learning are concerned with changes in neuronal sensitivity or changes in the way a stimulus is represented. Another possibility is that different areas of the brain are involved in performing a task while learning it and after learning it. Here we demonstrate that the right parietal cortex is involved in novel but not learned visual conjunction search. We observed that single pulse transcranial magnetic stimulation (TMS) to the right parietal cortex impairs visual conjunction search when the stimuli are novel and require a serial search strategy, but not once the particular search task has been learned. The effect of TMS returns when a different, novel, serial search task is presented.

Attention↗
PubMed1998

Learning from the pupil: a spatial visual channel in the absence of V1 in monkey and human.

The pupil of the normal human subject constricts in response not only to average increases in light energy, but also selectively to the spatial structure of a visual stimulus even when there are no energy changes. This enables one to measure visual acuity and sensitivity as a function of spatial frequency. It is known that pupillometric measures of acuity correlate well with those determined psychophysically for normal human observers. The purpose of the present study was to measure pupillary changes with stimuli delivered to the 'blind' hemifields of monkeys with unilateral V1 removal, and also with stimulation of a human subject (G.Y.) with putative V1 destruction. The results show that there are small but reliable pupillary changes to flux-equated gratings in the blind fields both in monkeys and human. The response profile in both species is very similar: it is narrowly tuned, with a peak at approximately 1 cycle/degree and a cut-off acuity of approximately 7 or 8 cycles/degree, a significant reduction compared with the intact hemifield. The result also maps well onto the psychophysically determined spatiotemporal response profile to gratings in the blind field, as determined independently for G.Y. Thus, there is a narrowly tuned spatial visual channel that does not require the integrity of V1 in monkey or human. There was no evidence under these particular conditions in either monkeys or subject G.Y. of a pupillary response to an equiluminant change from white to green or red in the hemianopic field. The pupil holds promise as a non-verbal, indirect method for determining the spatial profile, sensitivity and other properties of residual visual capacity, both in animals and humans.

Adult↗
PubMed1998

Retinal nerve fibre layer polarimetry: histological and clinical comparison.

AIMS: To compare histological thickness of the retinal nerve fibre layer in the primate with retardation measurements obtained in vivo using the Mark II Nerve Fiber Analyzer (NFA, Laser Diagnostic Technologies, San Diego, USA). METHODS: Scanning laser polarimetry was performed on both eyes of a healthy anaesthetised adult primate (Macaca mulatta). The retinal nerve fibre layer thickness was measured in the eye with the best polarimetry image. A nerve fibre layer thickness map was scaled and aligned to a retardation map to permit correlation of retardation and thickness measurements. RESULTS: Retinal nerve fibre layer thickness measurements could be satisfactorily aligned with corresponding retardation values at 216 locations. The overall correlation coefficient for nerve fibre layer thickness and retardation was r = 0.70 (n = 216, p < 0.001). Regional comparison showed the best correlation (r = 0.76, n = 45, p < 0.001) occurred inferior to the optic disc. Less positive but still highly significant correlations were seen superiorly and temporally (r = 0.52, n = 26, p = 0.007 and r = 0.49, n = 86, p = < 0.001 respectively), with the lowest correlation occurring at the nasal aspect of the disc (r = 0.06, n = 67, p = 0.64). CONCLUSIONS: In the primate eye, retinal nerve fibre layer thickness shows a positive correlation with retardation measurements obtained with the nerve fibre analyser. However, since the correlation coefficient varied around the optic disc, further evaluation of the device is advised before its routine clinical use.

Animals↗
PubMed1997

Is blindsight like normal, near-threshold vision?

Blindsight is the rare and paradoxical ability of some human subjects with occipital lobe brain damage to discriminate unseen stimuli in their clinically blind field defects when forced-choice procedures are used, implying that lesions of striate cortex produce a sharp dissociation between visual performance and visual awareness. Skeptics have argued that this is no different from the behavior of normal subjects at the lower limits of conscious vision, at which such dissociations could arise trivially by using different response criteria during clinical and forced-choice tests. We tested this claim explicitly by measuring the sensitivity of a hemianopic patient independently of his response criterion in yes-no and forced-choice detection tasks with the same stimulus and found that, unlike normal controls, his sensitivity was significantly higher during the forced-choice task. Thus, the dissociation by which blindsight is defined is not simply due to a difference in the patients' response bias between the two paradigms. This result implies that blindsight is unlike normal, near-threshold vision and that information about the stimulus is processed in blindsighted patients in an unusual way.

Adult↗