Abstract

Understanding how the brain forms representations of structured information distributed in time is a challenging endeavour for the neuroscientific community, requiring computationally and neurobiologically informed approaches. The neural mechanisms for segmenting continuous streams of sensory input and establishing representations of dependencies remain largely unknown, as do the transformations and computations occurring between the brain regions involved in these aspects of sequence processing. We propose a blueprint for a neurobiologically informed and informing computational model of sequence processing (entitled: Vector-symbolic Sequencing of Binding INstantiating Dependencies, or VS-BIND). This model is designed to support the transformation of serially ordered elements in sensory sequences into structured representations of bound dependencies, readily operates on multiple timescales, and encodes or decodes sequences with respect to chunked items wherever dependencies occur in time. The model integrates established vector symbolic additive and conjunctive binding operators with neurobiologically plausible oscillatory dynamics, and is compatible with modern spiking neural network simulation methods. We show that the model is capable of simulating previous findings from structured sequence processing tasks that engage fronto-temporal regions, specifying mechanistic roles for regions such as prefrontal areas 44/45 and the frontal operculum during interactions with sensory representations in temporal cortex. Finally, we are able to make predictions based on the configuration of the model alone that underscore the importance of serial position information, which requires input from time-sensitive cells, known to reside in the hippocampus and dorsolateral prefrontal cortex.This article is part of the theme issue ‘Towards mechanistic models of meaning composition’.

Highlights

  • Natural environments are richly structured in both space and time

  • Prior research has established the importance of serial order for the brain [4], and binding problems, whereby distinct sensory events are combined for perception, decision and action [5], have attracted considerable interest and empirical enquiry [6,7]

  • We propose a blueprint for a neurobiologically informed and informing computational model of sequence processing

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Summary

Introduction

Natural environments are richly structured in both space and time. Substantial progress has been made in understanding the neurobiological bases of learned relationships between spatially or temporally separated elements [1,2,3]. The VS-BIND approach integrates: (1) advances in modelling combinatorial binding within simulated neural systems using vector symbolic operations; (2) insights from neuroimaging and neurophysiological evidence in human and non-human primates on neural correlates of structured sequence processing and working memory; and (3) dynamic mechanisms for manipulating population codes that can be incorporated in modern spiking neural networks [21,22]. The approach allows us to plausibly transform internal representations, rendering these into both mathematically idealized and neurally simulated site-specific activity unfolding over time Building on these foundational mechanisms, we focus on modelling chunk encoding and the binding of sensory items to represent adjacent, non-adjacent and more complex (hierarchically) structured sequencing dependencies. Our use of VSAs has the benefit of generating predictions on neural mechanisms of combinatorial binding throughout the fronto-temporal system involved in structured sequence processing. We conclude by describing the role of these mechanisms within a neurobiologically plausible model of structured sequence processing, VS-BIND

Combinatorial population coding with vector symbolic architectures
Dynamically coordinating combinatorial operations with temporal mechanisms
Network-level mechanistic hypotheses derived from VS-BIND
B1 hierarchical relationships
In conclusion: predictions emerging from the structure of VS-BIND
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