Co-Planar Stereotaxic Atlas of the Human Brain—3-Dimensional Proportional System: An Approach to Cerebral Imaging, J. Talairach, P. Tournoux. Georg Thieme Verlag, New York (1988), 122 pp., 130 figs. DM 268

How to Do Things With Words

Functional magnetic resonance imaging (fMRI) is currently the mainstay of neuroimaging in cognitive neuroscience. Advances in scanner technology, image acquisition protocols, experimental design, and analysis methods promise to push forward fMRI from mere cartography to the true study of brain organization. However, fundamental questions concerning the interpretation of fMRI data abound, as the conclusions drawn often ignore the actual limitations of the methodology. Here I give an overview of the current state of fMRI, and draw on neuroimaging and physiological data to present the current understanding of the haemodynamic signals and the constraints they impose on neuroimaging data interpretation.

What we can do and what we cannot do with fMRI

Over the past 20 years, neuroimaging has become a predominant technique in systems neuroscience. One might envisage that over the next 20 years the neuroimaging of distributed processing and connectivity will play a major role in disclosing the brain's functional architecture and operational principles. The inception of this journal has been foreshadowed by an ever-increasing number of publications on functional connectivity, causal modeling, connectomics, and multivariate analyses of distributed patterns of brain responses. I accepted the invitation to write this review with great pleasure and hope to celebrate and critique the achievements to date, while addressing the challenges ahead.

/pdf/functional-and-effective-connectivity-a-review-s5oik3vige.pdf

Functional and effective connectivity: a review.

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An Introduction To The Event Related Potential Technique

Manipulating the characteristics of visual stimuli that simulate self-motion through the environment can affect the resulting postural sway magnitude. In the present study, we address the question whether varying the contrast and speed of a linear translating dot pattern influences medial–lateral postural sway. In a first experiment, we investigated whether the postural sway magnitude increases with increasing dot speed, as was previously demonstrated for expanding and contracting stimuli. In a second experiment, we also manipulated the contrast of the stimuli. For reasons that high-contrast stimuli can be considered ‘perceptually’ stronger, we expect that higher-contrast stimuli induce more sway than lower-contrast stimuli. The results of the first experiment show that dot speed indeed influences postural sway, although in an unexpected way. For higher speeds, the sway is in the direction of the stimulus motion, yet for lower speeds the sway is in a direction opposite to the stimulus motion. The results of the second experiment show that dot contrast does affect postural sway, but that this depends on the speed of the moving dots. Interestingly, the direction of postural sway induced by a relatively low dot speed (4°/s) depends on dot contrast. Taken together, our results suggest that interactions between the visual, vestibular and proprioceptive system appear to be influenced by an internal representation of the visual stimulus, rather than being influenced by the external visual stimulus characteristics only.

/pdf/interaction-effects-of-visual-stimulus-speed-and-contrast-on-4oca21yc7c.pdf

Interaction effects of visual stimulus speed and contrast on postural sway

Several models of selection in search predict that saccades are biased toward conspicuous objects (also referred to as salient objects). Indeed, it has been demonstrated that initial saccades are biased toward the most conspicuous candidate. However, in a recent study, no such bias was found for the second saccade, and it was concluded that the attraction of conspicuous elements is limited to only short-latency initial saccades. This conclusion is based on only a single feature manipulation (orientation contrast) and conflicts with the prediction of influential salience models. Here, we investigate whether this result can be generalized beyond the domain of orientation. In displays containing three luminance annuli (Experiment 1), we find a considerable bias toward the most conspicuous candidate for the second saccade. In Experiment 1, the target could not be discriminated peripherally. When we made the target peripherally discriminable, the second saccade was no longer biased toward the more conspicuous candidate (Experiment 2). Thus, conspicuity plays a role in saccadic selection beyond the initial saccade. Whether second saccades are biased toward conspicuous objects appears to depend on the type of feature contrast underlying the conspicuity and the peripheral discriminability of target properties.

https://journals.sagepub.com/doi/pdf/10.1177/0301006617735726

The Lifetime of Salience Extends Beyond the Initial Saccade.

Motion sensitivity changes due to motion adaptation in cat area 17 complex cells

Our movements can be guided directly by spatial information, but also more flexibly through arbitrary rules. We have recently shown that as arbitrary visuomotor mappings became overlearned, they come to rely not only on fronto-striatal circuits, but also on the posterior parietal cortex (PPC). Since this region supports multiple reference frames for hand movements, the question arose whether overlearned visuomotor associations could come to rely on a spatial framework, similar to spatially guided movements. Alternatively, overlearned visuomotor associations could be non-spatial in nature. In this study we investigate the characteristics of the movement representations supporting arbitrary visuomotor mappings by assessing how performance of extensively trained arbitrary visuomotor associations depends on the effector used to provide the response. After extensive training on a set of arbitrary visuomotor associations, subjects were asked to perform the same task in one of two novel settings that varied either the spatial or the motor relationship between visual instructions and finger movements. We found that the change in spatial configuration resulted in a larger amount of interference on the performance of the original mappings than the configuration change in motor coordinates. This result suggests that the visual stimuli became arbitrarily coupled to locations in space and not directly to the finger movements. We infer that overlearned arbitrary visuomotor associations are represented in spatial coordinates, in an effector-independent framework. This result raises the possibility that the previously reported involvement of the posterior parietal cortex in overlearned visuomotor behavior reflects the transition from an arbitrary visuomotor mapping into a spatially based stimulus-location-response mapping.

/pdf/spatial-representation-of-overlearned-arbitrary-visuomotor-5ftekol61d.pdf

Spatial representation of overlearned arbitrary visuomotor associations

Presenting a large optic flow pattern to observers is likely to cause postural sway. However, directional anisotropies have been reported, in that contracting optic flow induces more postural sway than expanding optic flow. Recently, we showed that the biomechanics of the lower leg cannot account for this anisotropy (Holten, Donker, Verstraten, & van der Smagt, 2013, Experimental Brain Research, 228, 117-129). The question we address in the current study is whether differences in visual processing of optic flow directions, in particular the perceptual strength of these directions, mirrors the anisotropy apparent in postural sway. That is, can contracting optic flow be considered to be a perceptually stronger visual stimulus than expanding optic flow? In the current study we use a breaking continuous flash suppression paradigm where we assume that perceptually stronger visual stimuli will break the flash suppression earlier, making the suppressed optic flow stimulus visible sooner. Surprisingly, our results show the opposite, in that expanding optic flow is detected earlier than contracting optic flow.

/pdf/visual-directional-anisotropy-does-not-mirror-the-4j9d23izo0.pdf

Frans A. J. Verstraten

Papers

Interaction effects of visual stimulus speed and contrast on postural sway

The Lifetime of Salience Extends Beyond the Initial Saccade.

Motion sensitivity changes due to motion adaptation in cat area 17 complex cells

Spatial representation of overlearned arbitrary visuomotor associations

Visual directional anisotropy does not mirror the directional anisotropy apparent in postural sway.