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Journal Article

Spatial Organization of Multisensory Responses in Temporal Association Cortex

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Dahl,  CD
Department Physiology of Cognitive Processes, Max Planck Institute for Biological Cybernetics, Max Planck Society;
Department Human Perception, Cognition and Action, Max Planck Institute for Biological Cybernetics, Max Planck Society;
Max Planck Institute for Biological Cybernetics, Max Planck Society;

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Logothetis,  NK
Department Physiology of Cognitive Processes, Max Planck Institute for Biological Cybernetics, Max Planck Society;
Max Planck Institute for Biological Cybernetics, Max Planck Society;

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Kayser,  C
Department Physiology of Cognitive Processes, Max Planck Institute for Biological Cybernetics, Max Planck Society;
Research Group Physiology of Sensory Integration, Max Planck Institute for Biological Cybernetics, Max Planck Society;
Max Planck Institute for Biological Cybernetics, Max Planck Society;

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Citation

Dahl, C., Logothetis, N., & Kayser, C. (2009). Spatial Organization of Multisensory Responses in Temporal Association Cortex. The Journal of Neuroscience, 29(38), 11924-11932. doi:10.1523/JNEUROSCI.3437-09.2009.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0013-C2F2-6
Abstract
Neurons in sensory cortices are often topographically organized according to their response preferences. We here show that such an organization of response preferences also exists in multisensory association cortex. Using electrophysiological mappings we probed the modality preference to auditory and visual stimuli of neurons in the superior temporal association cortex of non-human primates. We found that neurons preferring the same modality (auditory or visual) often co-occur in close spatial proximity, or occur intermingled with bimodal neurons. Neurons preferring different modalities, in contrast, occur spatially separated. This organization at the scale of individual neurons leads to extended patches of same modality preference when analyzed at the scale of millimeters, revealing larger scale regions that preferentially respond to the same modality. In addition, we find that neurons exhibiting signs of multisensory interactions, such as super- or sub-additive response summation, also occur in spatial clus
ters. Together, these results reveal a spatial organization of modality preferences in a higher association cortex, and lend support to the notion that topographical organizations might serve as a general principle of integrating information within and across the sensory modalities.