J. Scott McDonald

Orientation anisotropies in human visual cortex.

Representing the orientation of features in the visual image is a fundamental operation of the early cortical visual system. The nature of such representations can be informed by considering anisotropic distributions of response across the range of orientations. Here we used functional MRI to study modulations in the cortical activity elicited by observation of a sinusoidal grating that varied in orientation. We report a significant anisotropy in the measured blood-oxygen level-dependent activity within visual areas V1, V2, V3, and V3A/B in which horizontal orientations evoked a reduced response. These visual areas and hV4 showed a further anisotropy in which increased responses were observed for orientations that were radial to the point of fixation. We speculate that the anisotropies in cortical activity may be related to anisotropies in the prevalence and behavioral relevance of orientations in typical natural environments.

The influence of global form on local orientation anisotropies in human visual cortex.

Perception of the spatial structure of the environment results from visual system processes which integrate local information to produce global percepts. Here, we investigated whether particular global spatial arrangements evoke greater responses in the human visual system, and how such anisotropies relate to those evident in the responses to the local elements that comprise the global form. We presented observers with Glass patterns; images composed of randomly positioned dot pairings (dipoles) spatially arranged to produce a percept of translational or polar global form. We used functional magnetic resonance imaging (fMRI) to infer the magnitude of neural activity within early retinotopic regions of visual cortex (V1, V2, V3, V3A/B, and hV4) while the angular arrangement of the dipoles was modulated over time to sample the range of orientations. For both translational and polar Glass patterns, V1 showed an increased response to vertical dipole orientations and all visual areas showed a bias towards dipole orientations that were radial to the point of fixation. However, areas V1, V2, V3, and hV4 also demonstrated a bias, only present for polar Glass patterns, towards dipole orientations that were tangential to the point of fixation. This enhanced response to tangential orientations within polar form indicates sensitivity to curvature or more global form characteristics as early as primary visual cortex.

Orientation-specific contextual modulation of the fMRI BOLD response to luminance and chromatic gratings in human visual cortex.

The responses of orientation-selective neurons in primate visual cortex can be profoundly affected by the presence and orientation of stimuli falling outside the classical receptive field. Our perception of the orientation of a line or grating also depends upon the context in which it is presented. For example, the perceived orientation of a grating embedded in a surround tends to be repelled from the predominant orientation of the surround. Here, we used fMRI to investigate the basis of orientation-specific surround effects in five functionally-defined regions of visual cortex: V1, V2, V3, V3A/LO1 and hV4. Test stimuli were luminance-modulated and isoluminant gratings that produced responses similar in magnitude. Less BOLD activation was evident in response to gratings with parallel versus orthogonal surrounds across all the regions of visual cortex investigated. When an isoluminant test grating was surrounded by a luminance-modulated inducer, the degree of orientation-specific contextual modulation was no larger for extrastriate areas than for V1, suggesting that the observed effects might originate entirely in V1. However, more orientation-specific modulation was evident in extrastriate cortex when both test and inducer were luminance-modulated gratings than when the test was isoluminant; this difference was significant in area V3. We suggest that the pattern of results in extrastriate cortex may reflect a refinement of the orientation-selectivity of surround suppression specific to the colour of the surround or, alternatively, processes underlying the segmentation of test and inducer by spatial phase or orientation when no colour cue is available.

Failure of colour and contrast polarity identification at threshold for detection of motion and global form

We used identification at threshold to systematically measure binding costs in two visual modalities. We presented a conjunction of two features as a signal stimulus and concurrently measured detection and identification performance as a function of three threshold variables: duration, contrast and coherence. Discrepancies between detection and identification sensitivity functions demonstrated a consistent processing cost to visual feature binding. Our findings suggest that feature binding is indeed a genuine problem for the brain to solve. This simple paradigm can transfer across arbitrary feature combinations and is therefore suitable to use in experiments addressing mechanisms of sensory integration.

Synesthetes show normal sound-induced flash fission and fusion illusions

Idiopathic synesthesia, a neurological condition in which a stimulus in one sense generates a concurrent experience in a different sense, is often considered an example of multisensory integration. Consequently it has been suggested that synesthetes should experience multisensory illusions more consistently and compellingly than typical participants. To test this we measured the sound induced flash fission and fusion illusions in 22 coloured hearing synesthetes and 31 control participants. Analysis of the data using signal detection analysis, however, indicated no difference between the groups, either in perception or response bias, but a secondary analysis of the data did show evidence of a decline in the illusions for synesthetes with increasing age.

Gain control in the response of human visual cortex to plaids

A recent intrinsic signal optical imaging study in tree shrew showed, surprisingly, that the population response of V1 to plaid patterns comprising grating components of equal contrast is predicted by the average of the responses to the individual components (MacEvoy SP, Tucker TR, Fitzpatrick D. Nat Neurosci 12: 637-645, 2009). This prompted us to compare responses to plaids and gratings in human visual cortex as a function of contrast and orientation. We found that the functional MRI (fMRI) blood oxygenation level-dependent (BOLD) responses of areas V1-V3 to a plaid comprising superposed grating components of equal contrast are significantly higher than the responses to a single component. Furthermore, the orientation response profile of a plaid is poorly predicted from a linear combination of the responses to its components. Together, these results indicate that the model of MacEvoy et al. (2009) cannot, without modification, account for the fMRI BOLD response to plaids in human visual cortex.

Rapid serial visual presentation of motion: Short-term facilitation and long-term suppression

The visual system can detect coherent motion in the midst of motion noise. This is accomplished with motion-sensitive channels, each of which is tuned to a limited range of motion directions. Our aim was to show how a single channel is affected by motions both within and outside its tuning range. We used a psychophysical reverse-correlation procedure. An array of dots moved coherently with a new, randomly chosen, direction every 14 or 28 ms. Human subjects pressed a key whenever they saw upwards movement. The results were analyzed by finding two motion directions before each key-press: the first preceded the key-press by the reaction time, and the second preceded the first by a variable interval. There were two main findings. First, the subject was significantly more likely to press the key when the vector average of the two motions was in the target direction. This effect was short-lived: it was only seen for inter-stimulus intervals of several tens of milliseconds. Second, motion detection was reduced when the target direction was preceded by a motion of similar direction 100-200 ms earlier. The results support the idea that a motion-sensitive channel sums sub-optimal inputs, and is suppressed by similar motion in the long term.