Abstract

The primary electrophysiological marker of feature-based selection is the N2pc, a lateralized posterior negativity emerging around 180–200 ms. As it relies on hemispheric differences, its ability to discriminate the locus of focal attention is severely limited. Here we demonstrate that multivariate analyses of raw EEG data provide a much more fine-grained spatial profile of feature-based target selection. When training a pattern classifier to determine target position from EEG, we were able to decode target positions on the vertical midline, which cannot be achieved using standard N2pc methodology. Next, we used a forward encoding model to construct a channel tuning function that describes the continuous relationship between target position and multivariate EEG in an eight-position display. This model can spatially discriminate individual target positions in these displays and is fully invertible, enabling us to construct hypothetical topographic activation maps for target positions that were never used. When tested against the real pattern of neural activity obtained from a different group of subjects, the constructed maps from the forward model turned out statistically indistinguishable, thus providing independent validation of our model. Our findings demonstrate the power of multivariate EEG analysis to track feature-based target selection with high spatial and temporal precision.

Highlights

  • The primary electrophysiological marker of feature-based selection is the N2pc, a lateralized posterior negativity emerging around 180–200 ms

  • Feature-based attention serves to select relevant input from competing information. This is most prominent during visual search, when observers look for target objects among distractors, and selective attention is guided on the basis of target-defining features e.g. ref

  • The topography of early visual event-related potential (ERP) components varies with the location of a single visual stimulus in an otherwise empty visual field[4], it is more challenging to discriminate the position of attended objects in multi-stimulus visual search displays using EEG/MEG markers

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Summary

Introduction

The primary electrophysiological marker of feature-based selection is the N2pc, a lateralized posterior negativity emerging around 180–200 ms As it relies on hemispheric differences, its ability to discriminate the locus of focal attention is severely limited. We used a forward encoding model to construct a channel tuning function that describes the continuous relationship between target position and multivariate EEG in an eightposition display This model can spatially discriminate individual target positions in these displays and is fully invertible, enabling us to construct hypothetical topographic activation maps for target positions that were never used. The N2pc is an enhanced negativity elicited around 200 ms post-stimulus at posterior electrodes contralateral to candidate target objects e.g. refs 5 and 6 It is generated in extrastriate ventral visual cortex[7], and is assumed to reflect the spatially selective enhancement of neural activity during feature-based target selection see refs 8 and 9 for details. We employed two types of multivariate www.nature.com/scientificreports/

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