Abstract

Current neurobiological accounts of language and cognition offer diverging views on the questions of ‘where’ and ‘how’ semantic information is stored and processed in the human brain. Neuroimaging data showing consistent activation of different multi‐modal areas during word and sentence comprehension suggest that all meanings are processed indistinctively, by a set of general semantic centres or ‘hubs’. However, words belonging to specific semantic categories selectively activate modality‐preferential areas; for example, action‐related words spark activity in dorsal motor cortex, whereas object‐related ones activate ventral visual areas. The evidence for category‐specific and category‐general semantic areas begs for a unifying explanation, able to integrate the emergence of both. Here, a neurobiological model offering such an explanation is described. Using a neural architecture replicating anatomical and neurophysiological features of frontal, occipital and temporal cortices, basic aspects of word learning and semantic grounding in action and perception were simulated. As the network underwent training, distributed lexico‐semantic circuits spontaneously emerged. These circuits exhibited different cortical distributions that reached into dorsal‐motor or ventral‐visual areas, reflecting the correlated category‐specific sensorimotor patterns that co‐occurred during action‐ or object‐related semantic grounding, respectively. Crucially, substantial numbers of neurons of both types of distributed circuits emerged in areas interfacing between modality‐preferential regions, i.e. in multimodal connection hubs, which therefore became loci of general semantic binding. By relating neuroanatomical structure and cellular‐level learning mechanisms with system‐level cognitive function, this model offers a neurobiological account of category‐general and category‐specific semantic areas based on the different cortical distributions of the underlying semantic circuits.

Highlights

  • Current semantic theories offer diverging perspectives on how word meaning is acquired, represented and processed in the human brain

  • cell assemblies’ (CAs) circuits of the two semantic types exhibit similar distributions over the perisylvian cortex, with the highest CA-cell densities emerging in the multimodal areas PFi and PB

  • Only the ‘auditory’ component of a learnt sensorimotor wordpattern was presented as input to the network, causing the ‘ignition’ of the CA circuit that had emerged for that specific word

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Summary

Introduction

Current semantic theories offer diverging perspectives on how word meaning is acquired, represented and processed in the human brain. A putative brain basis for such a system of symbolic-conceptual representations has been attributed to ‘semantic hubs’, higher-association multimodal areas located in frontal, temporal and parietal cortices that have been found active during, or even to be necessary for, semantic processing (Price, 2000; Bookheimer, 2002; Devlin et al, 2003; Vigneau et al, 2006; Patterson et al, 2007; Binder & Desai, 2011; Pulverm€uller, 2013). Symbols are used to speak about specific objects, actions and other entities; access to such semantic knowledge likely involves processing sensorimotor information in modality-preferential areas of the cortex: for example, understanding an object-related word such as ‘cat’ should reactivate visual areas, whereas an action word like ‘grasp’ motor ones. Word and sentence comprehension induce category-specific activations in modality-preferential motor and sensory (visual, auditory, olfactory and gustatory) areas (Barsalou, 2008; Binder & Desai, 2011; Kiefer & Pulverm€uller, 2012; Pulverm€uller, 2013; Kemmerer, 2015)

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