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Reviewing the functional basis of the syntactic Merge mechanism for language: A coordinate-based activation likelihood estimation meta-analysis

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Zaccarella,  Emiliano
Department Neuropsychology, MPI for Human Cognitive and Brain Sciences, Max Planck Society;

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Schell,  Marianne
Department Neuropsychology, MPI for Human Cognitive and Brain Sciences, Max Planck Society;

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Friederici,  Angela D.
Department Neuropsychology, MPI for Human Cognitive and Brain Sciences, Max Planck Society;

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Citation

Zaccarella, E., Schell, M., & Friederici, A. D. (2017). Reviewing the functional basis of the syntactic Merge mechanism for language: A coordinate-based activation likelihood estimation meta-analysis. Neuroscience and Biobehavioral Reviews, 80, 646-656. doi:10.1016/j.neubiorev.2017.06.011.


Cite as: https://hdl.handle.net/11858/00-001M-0000-002D-CECC-4
Abstract
The ability to create structures out of single words is a key aspect of human language. This combinatorial capacity relies on a low-level syntactic mechanism—Merge—assembling words into hierarchies. Neuroscience has explored Merge by comparing syntax to word-lists. Here, we first review potential issues with the word-lists materials. We then perform an activation likelihood estimation (ALE) on the reported foci, to reveal functional convergence for Merge at whole-brain level. Finally, we run probabilistic tractography on an independent population to observe how these convergent activations anatomically connect. Functionally, we found that when confounding activity was removed, consistency for Merge was only observable in the left pars opercularis (BA44) and in the inferior part of the posterior superior temporal sulcus/gyrus (pSTS/STG; BA22). Structurally, we could confirm that the two regions are connected through dorsal fiber bundles. We therefore suggest that the cortical implementation of linguistic Merge consists of a left fronto-temporal interaction between BA44 (syntactic processor) and pSTS/STG (integrative processor), which communicate to each other along dorsal white matter fascicles.