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Carter, O.

Publications and source records attributed to Carter, O..

4 recordsLinked to original sources

When Tagging Frequency Matters to Attention: Effects on SSVEPs, ERPs, and Cognitive Processing

Selective attention enables the prioritization of task-relevant information while managing distractors, and steady-state visual evoked potentials (SSVEPs) are widely used to track this process by tagging different visual objects at distinct flicker frequencies. However, whether the choice of tagging frequency itself influences other neural and cognitive measures remains unclear. Here, 27 participants performed detection and 1-back working memory tasks while a central target and peripheral distractors flickered at either 8.6 Hz or 12 Hz. The working memory task produced slower responses, more errors, and greater perceived difficulty than detection. Tagging frequency strongly shaped neural responses, with 8.6 Hz eliciting higher SSVEP signal-to-noise ratios than 12 Hz regardless of stimulus location. Nevertheless, stronger SSVEP responses for centrally attended stimuli were associated with fewer working memory errors and larger early visual ERP responses, while SSVEPs for attended and distractor stimuli were negatively correlated. In addition, the working memory task produced a larger P1-N1 peak-to-peak difference, and tagging frequency altered the timing and amplitude of early ERP effects. Together, these findings show that tagging frequency is not a neutral methodological parameter, but one that shapes both neural indices of attention and their relationship to cognitive performance.

neuroscience↗

Multimodal lesion mapping in affective blindsight reveals dual amygdala and superior temporal sulcus contributions to nonconscious emotion processing

Affective blindsight, the capacity to discriminate emotional stimuli despite bilateral damage to the primary visual cortex (V1) and without conscious awareness, offers a unique model of non-conscious visual processing. Subcortical pathways involving the pulvinar and amygdala have been proposed, but putative cortical contributions remain unclear. We examined 182 patients, including 31 with bilateral V1 lesions. Among these, 15 had cortical visual loss and 7 showed affective blindsight. Using behavioral testing, lesion symptom mapping, and tractography, we found that preserved pulvinar connectivity with both the posterior superior temporal sulcus (STS) and the amygdala is necessary for affective blindsight. These findings provide causal evidence for a multi-route architecture, identifying the pulvinar-STS pathway, alongside the pulvinar-amygdala pathway, as a critical substrate for non-conscious affective processing.

neuroscience↗

Dynamical independence reveals anaesthetic specific fragmentation of emergent structure in neural dynamics

Conscious experience depends on the coordinated activity of neural processes that span multiple scales--from synapses to whole-brain dynamics. A recently introduced measure, dynamical independence, identifies, characterises and quantifies these multi-scale relationships using an information-theoretic dimensionality-reduction approach. Here, we use DI to examine changes in emergent dynamical structure in the human brain under three pharmacologically-distinct anaesthetic interventions (propofol, xenon, ketamine). Applied to source-reconstructed EEG, our analysis reveals that propofol and xenon, anaesthetics that abolish conscious report, exhibit more emergent but highly variable dynamic structure, indicating fragmented macroscopic dynamical organisation. By contrast, ketamine, which preserves dream-like phenomenology, shows the opposite pattern: reduced overall emergence yet a partial preservation of the macroscopic structure, mirroring wake. Further exploratory analyses revealed spatially localised source-level contributions to emergent dynamical structure, highlighting regional variations. Together, our results highlight drug-specific reconfigurations of emergent dynamical structure under anaesthesia, dissociate the amount of emergence from the organisation of emergent dynamics, and caution against equating emergence with level of consciousness.

neuroscience↗

Capturing the emergent dynamical structure in biophysical neural models

Complex neural systems can display structured emergent dynamics. Capturing this structure remains a significant scientific challenge. Using information theory, we apply Dynamical Independence (DI) to uncover the emergent dynamical structure in a minimal 5-node biophysical neural model, shaped by the interplay of two key aspects of brain organisation: integration and segregation. In our study, functional integration within the biophysical neural model is modulated by a global coupling parameter, while functional segregation is influenced by adding dynamical noise, which counteracts global coupling. DI defines a dimensionally-reduced macroscopic variable (e.g., a coarse-graining) as emergent to the extent that it behaves as an independent dynamical process, distinct from the micro-level dynamics. We measure dynamical dependence (a departure from dynamical independence) for macroscopic variables across spatial scales. Our results indicate that the degree of emergence of macroscopic variables is relatively minimised at balanced points of integration and segregation and maximised at the extremes. Additionally, our method identifies to which degree the macroscopic dynamics are localised across microlevel nodes, thereby elucidating the emergent dynamical structure through the relationship between microscopic and macroscopic processes. We find that deviation from a balanced point between integration and segregation results in a less localised, more distributed emergent dynamical structure as identified by DI. This finding suggests that a balance of functional integration and segregation is associated with lower levels of emergence (higher dynamical dependence), which may be crucial for sustaining coherent, localised emergent macroscopic dynamical structures. This work also provides a complete computational implementation for the identification of emergent neural dynamics that could be applied both in silico and in vivo. Author summaryUnderstanding how complex neural systems give rise to emergent macroscopic patterns is a central challenge in neuroscience. Emergence, where macroscopic structures appear from underlying microscopic interactions, plays a crucial role in brain function, yet identifying the specific dynamics involved remains elusive. Traditionally, methods have quantified the extent of emergence but have struggled to pinpoint the emergent dynamical structure itself. In this study, we develop and apply a method, based on a quantity called Dynamical Independence (DI), which simultaneously captures the extent of emergence and reveals the underlying dynamical structure in neurophysiological data. Using a minimal 5-node biophysical neural model, we explore how a balance between functional integration and segregation--two key organisational principles in the brain--affects emergent macroscopic dynamics. Our results show that a finely balanced system produces highly localised, coherent macroscopic structures, while extreme deviations lead to more distributed, less localised dynamics. This work provides a computational framework for identifying emergent dynamical structure in both theoretical models and potentially in empirical brain data, advancing our understanding of the brains complex organisation across higher-order scales.

neuroscience↗