Search PubMed⌕ Search

Biomedical subjects

Paul V McGraw

Publications and source records attributed to Paul V McGraw.

17 recordsLinked to original sources
PubMed2006

Resolving multisensory conflict: a strategy for balancing the costs and benefits of audio-visual integration.

In order to maintain a coherent, unified percept of the external environment, the brain must continuously combine information encoded by our different sensory systems. Contemporary models suggest that multisensory integration produces a weighted average of sensory estimates, where the contribution of each system to the ultimate multisensory percept is governed by the relative reliability of the information it provides (maximum-likelihood estimation). In the present study, we investigate interactions between auditory and visual rate perception, where observers are required to make judgments in one modality while ignoring conflicting rate information presented in the other. We show a gradual transition between partial cue integration and complete cue segregation with increasing inter-modal discrepancy that is inconsistent with mandatory implementation of maximum-likelihood estimation. To explain these findings, we implement a simple Bayesian model of integration that is also able to predict observer performance with novel stimuli. The model assumes that the brain takes into account prior knowledge about the correspondence between auditory and visual rate signals, when determining the degree of integration to implement. This provides a strategy for balancing the benefits accrued by integrating sensory estimates arising from a common source, against the costs of conflating information relating to independent objects or events.

Acoustic Stimulation↗
PubMed2005

Functional evidence for cone-specific connectivity in the human retina.

Physiological studies of colour vision have not yet resolved the controversial issue of how chromatic opponency is constructed at a neuronal level. Two competing theories, the cone-selective hypothesis and the random-wiring hypothesis, are currently equivocal to the architecture of the primate retina. In central vision, both schemes are capable of producing colour opponency due to the fact that receptive field centres receive input from a single bipolar cell - the so called 'private line arrangement'. However, in peripheral vision this single-cone input to the receptive field centre is lost, so that any random cone connectivity would result in a predictable reduction in the quality of colour vision. Behavioural studies thus far have indeed suggested a selective loss of chromatic sensitivity in peripheral vision. We investigated chromatic sensitivity as a function of eccentricity for the cardinal chromatic (L/M and S/(L + M)) and achromatic (L + M) pathways, adopting stimulus size as the critical variable. Results show that performance can be equated across the visual field simply by a change of scale (size). In other words, there exists no qualitative loss of chromatic sensitivity across the visual field. Critically, however, the quantitative nature of size dependency for each of the cardinal chromatic and achromatic mechanisms is very specific, reinforcing their independence in terms of anatomy and genetics. Our data provide clear evidence for a physiological model of primate colour vision that retains chromatic quality in peripheral vision, thus supporting the cone-selective hypothesis.

Adaptation, Physiological↗
PubMed2005

Spatial interactions reveal inhibitory cortical networks in human amblyopia.

Humans with amblyopia have a well-documented loss of sensitivity for first-order, or luminance defined, visual information. Recent studies show that they also display a specific loss of sensitivity for second-order, or contrast defined, visual information; a type of image structure encoded by neurons found predominantly in visual area A18/V2. In the present study, we investigate whether amblyopia disrupts the normal architecture of spatial interactions in V2 by determining the contrast detection threshold of a second-order target in the presence of second-order flanking stimuli. Adjacent flanks facilitated second-order detectability in normal observers. However, in marked contrast, they suppressed detection in each eye of the majority of amblyopic observers. Furthermore, strabismic observers with no loss of visual acuity show a similar pattern of detection suppression. We speculate that amblyopia results in predominantly inhibitory cortical interactions between second-order neurons.

Adult↗
PubMed2005

Chromatic masking revealed by the standing wave of invisibility illusion.

We have used the standing wave of invisibility illusion (Macknik and Livingstone, 1998 Nature Neuroscience 1 144-149) to examine the masking effects produced by a range of stimuli of varying chromatic and luminance contrast content. The pattern of masking was highly selective. Maximum effects were always obtained when the target and mask were identical in terms of their chromatic and/or luminance contrast composition, but were reduced as the angular separation in colour space between them was increased. Masking was of a monopolar nature, indicating the operation of rectified mechanisms selective for different combinations of colour and luminance contrast.

Color Perception↗
PubMed2005

A psychophysical investigation of ocular expansion in human eyes.

PURPOSE: To investigate spatial anisotropies in the peripheral visual field of axially myopic eyes, in an attempt to distinguish between models of isotropic and anisotropic ocular stretching. METHODS: Stimuli consisted of two high-contrast Gaussian patches presented in one of four orientations (90 degrees, 180 degrees, 45 degrees, or 135 degrees). For each orientation, perceived separation was established relative to that for all other orientations. The experiment was conducted with central fixation and at 15 degrees in the nasal and inferior visual fields. Eleven myopes and nine emmetropes participated in the study. Biometric data were collected from all subjects. RESULTS: For foveal fixation, the magnitude of the spatial anisotropy (approximately 5%) was consistent with the well-documented horizontal-vertical illusion (HVI), and unrelated to axial length. In the nasal visual field, much larger misperceptions were found (approximately 19%), the magnitude of which increased significantly with increasing axial length. Inferiorly, a reversal of the traditional HVI is found in most subjects (approximately 7%), with a tendency for a larger reversed illusion with increasing axial length. Differences between nasal and inferior misperceptions were significantly correlated with axial length. CONCLUSIONS: Isotropic stretching, such as globe expansion, should preserve the aspect ratios of receptive fields, predicting a separation misperception which is independent of axial length. In contrast, the magnitude of the misperception is significantly correlated with axial length, supporting anisotropic stretching models of myopic growth.

Elastic Tissue↗
PubMed2004

Positional adaptation reveals multiple chromatic mechanisms in human vision.

Precortical color vision is mediated by three independent opponent or cardinal mechanisms that linearly combine receptoral outputs to form L/M, S/(L+M), and L+M channels. However, data from a variety of psychophysical and physiological experiments indicate that chromatic processing undergoes a reorganization away from the basic opponent model. Frequently, this post-opponent reorganization is viewed in terms of the generation of multiple "higher order" chromatic mechanisms, tuned to a wide variety of axes in color space. Moreover, adaptation experiments have revealed that the synthesis of these mechanisms occurs at a level in the cortex following the binocular integration of the inputs from each eye. Here we report results from an experiment in which the influence of chromatic adaptation on the perceived visual location of a test stimulus was explored using a Vernier alignment task. The results indicate that not only is positional information processed independently within the L/M, S/(L+M), and L+M channels, but that when adapting and test stimuli are extended to non-cardinal axes, the existence of multiple chromatically tuned mechanisms is revealed. Most importantly, the effects of chromatic adaptation on this task exhibit little interocular transfer and have rapid decay rates, consistent with chromatic as opposed to contrast adaptation. These findings suggest that the reorganization of chromatic processing may take place earlier in the visual pathway than previously thought.

Adaptation, Ocular↗
PubMed2004

Motion-sensitive neurones in V5/MT modulate perceived spatial position.

Until recently, it was widely believed that object position and object motion were represented independently in the visual cortex. However, several studies have shown that adaptation to motion produces substantial shifts in the perceived position of subsequently viewed stationary objects. Two stages of motion adaptation have been proposed: an initial stage at the level of V1 and a secondary stage thought to be located in V5/MT. Indeed, selective adaptation can be demonstrated at each of these levels of motion analysis. What remains unknown is which of these cortical sites are involved in modulating the positional representation of subsequently viewed objects. To answer this question directly, we disrupted cortical activity by using transcranial magnetic stimulation (TMS) immediately after motion adaptation. When TMS was delivered to V5/MT after motion adaptation, the perceived offset of the test stimulus was greatly reduced. In marked contrast, TMS of V1 had no effect on the changes that normally occur in perceived position after motion adaptation. This result demonstrates that the anatomical locus at which motion and positional information interact is area V5/MT rather than V1/V2.

Brain Mapping↗
PubMed2004

Pulling the other one: 1st- and 2nd-order visual information interact to determine perceived location.

We demonstrate that the 1st- and 2nd-order characteristics of a visual stimulus can have a profound influence on each other in terms of perceived position. We use the parameter of spatial separation to selectively manipulate the effect of one characteristic upon the other. 1st-order features have their largest effect upon the perceived position of 2nd-order structure when separation is small, whilst the reciprocal effect is maximal at large separations. Implications for models of 1st- and 2nd-order interaction are discussed.

Cues↗
PubMed2004

Understanding the neural basis of amblyopia.

Amblyopia is the condition in which reduced visual function exists despite full optical correction and an absence of observable ocular pathology. Investigation of the underlying neurology of this condition began in earnest around 40 years ago with the pioneering studies conducted by Hubel and Wiesel. Their early work on the impact of monocular deprivation and strabismus initiated what is now a rapidly developing field of cortical plasticity research. Although the monocular deprivation paradigm originated by Hubel and Wiesel remains a key experimental manipulation in studies of cortical plasticity, somewhat ironically, the neurology underlying the human conditions of strabismus and amblyopia that motivated this early work remains elusive. In this review, the authors combine contemporary research on plasticity and development with data from human and animal investigations of amblyopic populations to assess what is known and to reexamine some of the key assumptions about human amblyopia.

Amblyopia↗
PubMed2003

Deficits to global motion processing in human amblyopia.

We investigated global motion processing in a group of adult amblyopes using a method that allows us to factor out any influence of the known contrast sensitivity deficit. We show that there are independent global motion processing deficits in human amblyopia that are unrelated to the contrast sensitivity deficit, and that are more extensive for contrast-defined than for luminance-defined stimuli. We speculate that the site of these deficits must include the extra-striate cortex and in particular the dorsal pathway.

Adult↗
PubMed2003

Neither here nor there: localizing conflicting visual attributes.

Natural visual scenes are a rich source of information. Objects often carry luminance, colour, motion, depth and textural cues, each of which can serve to aid detection and localization of the object within a scene. Contemporary neuroscience presumes a modular approach to visual analysis in which each of these attributes are processed within ostensibly independent visual streams and are transmitted to geographically distinct and functionally dedicated centres in visual cortex (van Essen & Maunsell, 1983; Zihl, von Cramon & Mai, 1983; Maunsell & Newsome, 1987; Tootell, Hadjikhani, Mendola, Marrett & Dale, 1998). In the present study we ask how the visual system localizes objects within this framework. Specifically, we investigate how the visual system assigns a unitary location to objects defined by multiple stimulus attributes, where such attributes provide conflicting positional cues. The results show that conflicting sources of visual information can be effortlessly combined to form a global estimate of spatial position, yet, this conflation of visual attributes is achieved at a cost to localization accuracy. Furthermore, our results suggest that the visual system assigns more perceptual weight (Landy, 1993; Landy & Kojima, 2001) to visual attributes which are reliably related to object contours.

Attention↗
PubMed2002

Motion adaptation distorts perceived visual position.

After an observer adapts to a moving stimulus, texture within a stationary stimulus is perceived to drift in the opposite direction-the traditional motion aftereffect (MAE). It has recently been shown that the perceived position of objects can be markedly influenced by motion adaptation. In the present study, we examine the selectivity of positional shifts resulting from motion adaptation to stimulus attributes such as velocity, relative contrast, and relative spatial frequency. In addition, we ask whether spatial position can be modified in the absence of perceived motion. Results show that when adapting and test stimuli have collinear carrier gratings, the global position of the object shows a substantial shift in the direction of the illusory motion. When the carrier gratings of the adapting and test stimuli are orthogonal (a configuration in which no MAE is experienced), a global positional shift of similar magnitude is found. The illusory positional shift was found to be immune to changes in spatial frequency and to contrast between adapting and test stimuli-manipulations that dramatically reduce the magnitude of the traditional MAE. The lack of sensitivity for stimulus characteristics other than direction of motion suggests that a specialized population of cortical neurones, which are insensitive to changes in a number of rudimentary visual attributes, may modulate positional representation in lower cortical areas.

Adaptation, Ocular↗
PubMed2002

Isolation of stimulus characteristics contributing to Weber's law for position.

To examine the independent contribution of various stimulus characteristics to positional judgements, we measured vernier alignment performance for three types of Gabor stimuli. In one, only the contrast envelope of the upper and lower stimulus elements was offset, with the luminance-modulated carrier grating remaining in alignment. In the second, only the carrier grating was offset. In the third, both carrier and envelope were offset together. Performance was examined over a range of element separations. When both cues are available, thresholds for small separations are dominated by carrier offset information and are inversely proportional to carrier frequency. At large separations, thresholds are governed by the spatial scale characteristics of the envelope. For broad-band stimuli such as lines, bars or dots typically used for vernier acuity, their higher frequency content can be used when separations are small, but as separation increases a smooth transition between the scales that determine threshold results in the continuum known as Weber's law for position. That is, with increasing separation, larger scales must be used, and thresholds increase in direct proportion to 1/frequency.

Contrast Sensitivity↗
PubMed2002

The importance of spatial scale in determining illusions of orientation.

The twisted-cord illusion is a powerful demonstration of interaction between 1st-order (luminance-defined) and 2nd-order (contrast-defined) orientation processing. The perceived orientation of contrast-defined objects is pulled towards their 1st-order orientation content when the difference in orientation is small (Fraser effect), yet is pushed away from the 1st-order content at large orientation differences (Zöllner effect). Here we show that the relative spatial scale of carrier and envelope represents a decisive factor in determining the magnitude and direction of such interactions. We conclude that the perceived 2nd-order structure of a stimulus is biased by the properties of the 1st-order structure in a manner that depends on relative, rather than absolute spatial scale.

Form Perception↗
PubMed2002

Perceived contrast following adaptation: the role of adapting stimulus visibility.

The issue of whether contrast adaptation can reduce the perceived contrast of gratings oriented orthogonal to the adapting stimulus to a greater extent than parallel gratings has been the subject of considerable debate (Snowden and Hammett, 1992; Ross and Speed, 1996). We compared the reductions in perceived contrast of various test gratings oriented parallel and orthogonal to the adapting stimulus across a range of spatial frequencies (2.25-9 c/deg) and adaptation contrasts (0.19-1.0). Our results show that when the adapting stimulus is low in contrast, parallel adaptation effects are always greater than the effects of orthogonal adaptation. When the adapting contrast is increased, however, the difference between parallel and orthogonal effects is reduced. Further increases in adapting contrast can produce a situation where cross-orientation adaptation effects exceed iso-orientation effects. This was observed at low spatial frequencies (2.25 and 4.5 c/deg) only. The difference in the pattern of results obtained at low and high spatial frequencies can be explained in terms of the adapting stimulus visibility. We conclude that cross-orientation adaptation effects can be greater than iso-orientation effects, but only when the adapting stimulus is highly suprathreshold.

Adaptation, Ocular↗