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Santo-Angles, A.

Publications and source records attributed to Santo-Angles, A..

2 recordsLinked to original sources

Neural Subspaces Encode Sequential Working Memory, but Neural Sequences Do Not

The neural mechanisms of multiple-item working memory are not well understood. In the current study, we address two competing hypotheses about the neural basis of sequential working memory: neural subspaces versus neural sequences. Using broadband MEG data from human participants, we applied dimensionality reduction and multivariate decoding techniques to test whether sequential items are maintained during the retention period through the reactivation of individual items in sequence (neural sequences), or by organizing them into distinct low-dimensional subspaces (neural subspaces). Our results revealed behaviorally relevant, low-dimensional neural subspaces that organized memory representations during the retention period but not during stimulus encoding, supporting the neural subspaces hypothesis. In contrast, we found no evidence of sequential neural replay during the delay period, contrary to predictions from the neural sequences hypothesis. Together, our findings suggest that sequential working memory is maintained through structured geometric organization in low-dimensional representational space, rather than through the sequential reactivation of individual items.

neuroscience↗

Alpha phase-coding supports feature binding during working memory maintenance

The ability to successfully retain and manipulate information in working memory (WM) requires that objects individual features are bound into cohesive representations; yet, the mechanisms supporting feature binding remain unclear. Binding (or swap) errors, where memorized features are erroneously associated with the wrong object, can provide a window into the intrinsic limits in capacity of WM that represent a key bottleneck in our cognitive ability. We tested the hypothesis that binding in WM is accomplished via neural phase synchrony and that swap errors result from perturbations in this synchrony. Using magnetoencephalography data collected from human subjects in a task designed to induce swap errors, we showed that swaps are characterized by reduced phase-locked oscillatory activity during memory retention, as predicted by an attractor model of spiking neural networks. Further, we found that this reduction arises from increased phase coding variability in the alpha-band over a distributed network of sensorimotor areas. Our findings demonstrate that feature binding in WM is accomplished through phase coding dynamics that emerge from the competition between different memories. SignificanceWe investigate the neural basis of working memory, focusing on how feature binding is accomplished and how binding or swap errors arise. Using magnetoencephalography, we found that stable phase-locking of alpha oscillations supports correct feature binding, while swap errors correlate with reduced alpha phase preservation, localized to specific brain areas. These findings align with a biologically-plausible computational model predicting that temporal synchrony in neuronal firing underpins feature binding. This work advances our understanding of the neural mechanisms of working memory, providing empirical support for theories of time-based binding and demonstrating the utility of biophysically-realistic models in human neuroimaging studies.

neuroscience↗