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Scrivener, C. L.

Publications and source records attributed to Scrivener, C. L..

9 recordsLinked to original sources

Scene perception-memory pairing extends to superior parietal cortex

Visual scene analysis relies on a set of scene-selective regions in posterior cerebral cortex (OPA, PPA, MPA), with a paired memory-responsive counterpart located in anterior (LPMA, VPMA) or overlapping cortex (MPMA). The interaction between these pairs of regions is thought to integrate visual input with mnemonic context. Recently, a fourth scene-perception area in superior parietal cortex (SPA) was identified, with a proposed role in visually-guided navigation. Whether this region also has an anterior paired memory region is currently unknown. Across two independent fMRI datasets (total N=24, 14 females) using static or dynamic stimuli and distinct memory tasks, we show that recalling visual scenes evokes robust responses in a region (referred to here as SPMA) immediately anterior and dorsal to SPA. During resting-state fMRI, SPA preferentially coupled with the other scene-perception areas, while SPMA preferentially coupled with the other place memory areas. At the whole-brain level, seed-based connectivity revealed that SPA sits at the confluence of four processing streams spanning regions implicated in egocentric scene perception, map-based navigation, perspective taking, and goal-directed movement. These findings extend the perception-memory motif associated with visual scene processing to the fourth cortical surface. The widespread anatomical coupling between scene-perception and memory processes reflects the importance of this interaction for flexible, context-grounded navigation.

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Visual imagery of familiar people and places in category selective cortex

Visual imagery is a dynamic process recruiting a network of brain regions. We used electroencephalography (EEG) and functional magnetic resonance imaging (fMRI) fusion to investigate the dynamics of category selective imagery in medial parietal cortex (MPC), ventral temporal cortex (VTC), and primary visual cortex (V1). Subjects attended separate EEG and fMRI sessions where they created mental images of personally familiar people and place stimuli. The fMRI contrast comparing people and place imagery replicated previous findings of category-selectivity in the medial parietal cortex. In addition, greater activity for places was found in the ventral and lateral place memory areas, the frontal eye fields, the inferior temporal sulcus, and the intraparietal sulcus. In contrast, greater activity for people was found in the fusiform face area and the right posterior superior temporal sulcus. Using multivariate decoding analysis in fMRI, we could decode individual stimuli within the preferred category in VTC. A more complex pattern emerged in MPC, which represented information that was not restricted to the preferred category. We were also able to decode category and individual stimuli in the EEG data. EEG-fMRI fusion indicated similar timings in MPC and VTC activity during imagery. However, in the VTC, fusion was higher in place selective regions during an early time window, and higher in face selective regions in a later time window. In contrast, fusion correlations in V1 occurred later during the imagery period, possibly reflecting the top-down progression of mental imagery from category-selective regions to primary visual cortex.

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Opponent visuospatial coding structures responses during memory recall and visual perception in medial parietal cortex

The mechanisms linking perceptual and memory representations in the brain are not yet fully understood. In early visual cortex, perception and memory are known to share similar neural representations, but how they interact beyond early visual cortex is less clear. Recent work identified that scene-perception and scene-memory areas on the lateral and ventral surfaces of the brain are linked via a shared but opponent visuospatial coding scheme, suggesting that shared visuospatial coding might provide a framework for perceptual-memory interactions. Here, we test whether the pattern in visuospatial coding within category-selective memory areas of medial parietal cortex structures responses during memory recall and visual perception. Using functional magnetic resonance imaging, we observe signatures of visuospatial coding in the form of population receptive fields (pRFs) with both positive and negative response profiles within medial parietal cortex. Crucially, the more dissimilar the timeseries of a pair of positive/negative pRFs within a region, the more dissimilar their responses during both memory recall and visual perception - tasks that place very different demands on these regions: internally oriented memory recall versus externally oriented visual perception. These data extend recent work to suggest that the interplay between pRFs with opponent visuospatial coding may play a vital role in integrating information across different representational spaces.

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Comparison of MR coil options for concurrent TMS-fMRI

Concurrent transcranial magnetic stimulation (TMS) with functional magnetic resonance imaging (fMRI) is increasingly being used to study how TMS affects neural processing in local and remote connected brain regions. However, there are many technical challenges that arise when operating this unique combination of techniques. One such challenge is MR head coil compatibility and the image resolution that can be achieved. Here we compare the temporal-signal-to noise-ratio (tSNR) between 3 different MR head coils that can be used with TMS. We show that the 7-channel TMS-dedicated surface coils result in a very high tSNR directly under the TMS and the supplementary coil in comparison to the TxRx and the Magnetica. However, there is low tSNR elsewhere. This field inhomogeneity may not be suitable for all research questions, for example where the aim is to look at distributed neural responses. In these cases, an MR coil with a more homogeneous tSNR such as the Magnetica, may be more appropriate.

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The causal roles of parietal alpha oscillations and evoked potentials in coding task-relevant information during selective attention

Selective attention is a fundamental cognitive mechanism that allows people to prioritise task-relevant information while ignoring irrelevant information. Previous research has suggested key roles of parietal evoked potentials and alpha oscillatory responses in spatial attention tasks. However, the informational content of these signals is less clear, and their causal effects on the coding of multiple task elements are yet unresolved. Here, we used concurrent TMS-EEG to causally manipulate parietal alpha power and evoked potentials and investigate their roles in coding multiple task features (where to attend, what to attend to, and visual stimulus) in a selective attention task. First, using EEG-only data, we found that evoked potentials coded all three types of task-relevant information with distinct temporal dynamics, and alpha oscillations carried information regarding both where to attend and what to attend to. Then, we applied rhythmic-TMS (rTMS) at individual alpha frequency over the right intraparietal sulcus (IPS), while concurrently measuring EEG. Compared with control arrhythmic-TMS, alpha rTMS increased alpha power and inter-trial phase coherence and yielded more negative posterior-contralateral evoked potentials. Moreover, alpha rTMS causally and specifically improved multivariate decoding of the information about where to attend (but not what to attend to or feature information) during task performance, with decoding improvements predicting changes in behavioural performance. These findings illuminate the dynamics with which the complementary aspects of a selective attention task are encoded in evoked and oscillatory brain activity. Moreover, they reveal a specific and causal role of IPS-controlled evoked and oscillatory activity in carrying behaviour-driving information about where to focus attention.

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Optimising analysis choices for multivariate decoding: creating pseudotrials using trial averaging and resampling

Multivariate pattern analysis (MVPA) is a popular technique that can distinguish between condition-specific patterns of activation. Applied to neuroimaging data, MVPA decoding for inference uses above chance decoding to identify statistically reliable condition-specific information in neuroimaging data which may be missed by univariate methods. However, several analysis choices influence decoding results, and the combined effects of these choices have not been fully evaluated. In particular, an increasingly popular approach is to average data from several trials together before training an MVPA classifier, but the decision about how much averaging to do is arbitrary and the effect of varying this parameter has not been documented. Here we systematically assessed the influence of trial averaging and resampling on decoding accuracy and subsequent statistical outcome on simulated data. Although the optimal parameters varied with the classifier and cross-validation approach used, we found that modest trial averaging using up to 5-10% of the total number of trials per condition improved decoding accuracy and associated t-statistics. In addition, a small amount of resampling could improve t-statistics and classification performance, but was not always necessary. We provide code to allow researchers to optimise these analysis choices for the parameters of their data.

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Now you see it, now you don't: optimal parameters for interslice stimulation in concurrent TMS-fMRI

The powerful combination of transcranial magnetic stimulation (TMS) concurrent with functional magnetic resonance imaging (fMRI) provides rare insights into the causal relationships between brain activity and behaviour. Despite a recent resurgence in popularity, TMS-fMRI remains technically challenging. Here we examined the feasibility of applying TMS during short gaps between fMRI slices to avoid incurring artefacts in the fMRI data. We quantified signal dropout and changes in temporal signal-to-noise ratio (tSNR) for TMS pulses presented at timepoints from 100ms before to 100ms after slice onset. Up to 3 pulses were delivered per volume using MagVentures MR-compatible TMS coil. We used a spherical phantom, two 7-channel TMS-dedicated surface coils, and a multiband (MB) sequence (factor=2) with interslice gaps of 100ms and 40ms, on a Siemens 3T Prisma-fit scanner. For comparison we repeated a subset of parameters with a more standard single-channel TxRx (birdcage) coil, and with a human participant and surface coil set up. We found that, even at 100% stimulator output, pulses applied at least - 40ms/+50ms from the onset of slice readout avoid incurring artifacts. This was the case for all three setups. Thus, an interslice protocol can be achieved with a frequency of up to ~10 Hz, using a standard EPI sequence (slice acquisition time: 62.5ms, interslice gap: 40ms). Faster stimulation frequencies would require shorter slice acquisition times, for example using in-plane acceleration. Interslice TMS-fMRI protocols provide a promising avenue for retaining flexible timing of stimulus delivery without incurring TMS artifacts.

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Variability of EEG electrode positions and their underlying brain regions: visualising gel artifacts from a simultaneous EEG-fMRI dataset

We investigated the between-subject variability of EEG electrode placement from a simultaneously recorded EEG-fMRI dataset. Neuro-navigation software was used to localise electrode positions in xyz and MNI space, made possible by the gel artifacts present in the structural MRI images. To assess variation in the brain regions directly underneath each electrode, we used both raw MNI coordinates and labels from the Harvard-Oxford Cortical atlas. In a sample of 20 participants, the mean standard deviation of electrode placement was 3.94 mm in x, 5.55 mm in y, and 7.17 mm in z, with the largest variation in parietal and occipital electrodes. In addition, the brain regions covered by electrode pairs was not always consistent; for example, the mean location of electrode P07 was mapped to BA18, whereas P08 was closer to BA19. Further, electrode C1 was mapped to the left primary motor cortex, whereas C2 was closer to right pre-motor cortex. Overall, the results emphasise the variation in electrode positioning that can be found even in a fixed cap, potentially caused by between-subject differences in brain morphology. We present a relatively simple method for approximating the location of electrodes in a simultaneous EEG-fMRI data set with accompanying analysis code, and suggest that researchers check the regions underlying their EEG ROIs to improve the generalisability and reliability of their neuroimaging results.

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An EEG study of detection without localisation in change blindness

Previous studies of change blindness have suggested a distinction between detection and localisation of changes in a visual scene. Using a simple paradigm with an array of coloured squares, the present study aimed to further investigate differences in event-related potentials (ERPs) between trials in which participants could detect the presence of a colour change but not identify the location of the change (sense trials), versus those where participants could both detect and localise the change (localise trials). Individual differences in performance were controlled for by adjusting the difficulty of the task in real time. Behaviourally, reaction times for sense, blind, and false alarm trials were distinguishable when comparing across levels of participant certainty. In the EEG data, we found no significant differences in the visual awareness negativity ERP, contrary to previous findings. In the N2pc range, both awareness conditions (localise and sense) were significantly different to trials with no change detection (blind trials), suggesting that this ERP is not dependent on explicit awareness. Within the late parietal positivity range, all conditions were significantly different. These results suggest that changes can be sensed without knowledge of the location of the changing object, and that participant certainty scores can provide valuable information about the perception of changes in change blindness.

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