Cargando…

Different computations over the same inputs produce selective behavior in algorithmic brain networks

A key challenge in neuroimaging remains to understand where, when, and now particularly how human brain networks compute over sensory inputs to achieve behavior. To study such dynamic algorithms from mass neural signals, we recorded the magnetoencephalographic (MEG) activity of participants who reso...

Descripción completa

Detalles Bibliográficos
Autores principales: Jaworska, Katarzyna, Yan, Yuening, van Rijsbergen, Nicola J, Ince, Robin AA, Schyns, Philippe G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8853655/
https://www.ncbi.nlm.nih.gov/pubmed/35174783
http://dx.doi.org/10.7554/eLife.73651
_version_ 1784653276741894144
author Jaworska, Katarzyna
Yan, Yuening
van Rijsbergen, Nicola J
Ince, Robin AA
Schyns, Philippe G
author_facet Jaworska, Katarzyna
Yan, Yuening
van Rijsbergen, Nicola J
Ince, Robin AA
Schyns, Philippe G
author_sort Jaworska, Katarzyna
collection PubMed
description A key challenge in neuroimaging remains to understand where, when, and now particularly how human brain networks compute over sensory inputs to achieve behavior. To study such dynamic algorithms from mass neural signals, we recorded the magnetoencephalographic (MEG) activity of participants who resolved the classic XOR, OR, and AND functions as overt behavioral tasks (N = 10 participants/task, N-of-1 replications). Each function requires a different computation over the same inputs to produce the task-specific behavioral outputs. In each task, we found that source-localized MEG activity progresses through four computational stages identified within individual participants: (1) initial contralateral representation of each visual input in occipital cortex, (2) a joint linearly combined representation of both inputs in midline occipital cortex and right fusiform gyrus, followed by (3) nonlinear task-dependent input integration in temporal-parietal cortex, and finally (4) behavioral response representation in postcentral gyrus. We demonstrate the specific dynamics of each computation at the level of individual sources. The spatiotemporal patterns of the first two computations are similar across the three tasks; the last two computations are task specific. Our results therefore reveal where, when, and how dynamic network algorithms perform different computations over the same inputs to produce different behaviors.
format Online
Article
Text
id pubmed-8853655
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-88536552022-02-22 Different computations over the same inputs produce selective behavior in algorithmic brain networks Jaworska, Katarzyna Yan, Yuening van Rijsbergen, Nicola J Ince, Robin AA Schyns, Philippe G eLife Neuroscience A key challenge in neuroimaging remains to understand where, when, and now particularly how human brain networks compute over sensory inputs to achieve behavior. To study such dynamic algorithms from mass neural signals, we recorded the magnetoencephalographic (MEG) activity of participants who resolved the classic XOR, OR, and AND functions as overt behavioral tasks (N = 10 participants/task, N-of-1 replications). Each function requires a different computation over the same inputs to produce the task-specific behavioral outputs. In each task, we found that source-localized MEG activity progresses through four computational stages identified within individual participants: (1) initial contralateral representation of each visual input in occipital cortex, (2) a joint linearly combined representation of both inputs in midline occipital cortex and right fusiform gyrus, followed by (3) nonlinear task-dependent input integration in temporal-parietal cortex, and finally (4) behavioral response representation in postcentral gyrus. We demonstrate the specific dynamics of each computation at the level of individual sources. The spatiotemporal patterns of the first two computations are similar across the three tasks; the last two computations are task specific. Our results therefore reveal where, when, and how dynamic network algorithms perform different computations over the same inputs to produce different behaviors. eLife Sciences Publications, Ltd 2022-02-17 /pmc/articles/PMC8853655/ /pubmed/35174783 http://dx.doi.org/10.7554/eLife.73651 Text en © 2022, Jaworska et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Jaworska, Katarzyna
Yan, Yuening
van Rijsbergen, Nicola J
Ince, Robin AA
Schyns, Philippe G
Different computations over the same inputs produce selective behavior in algorithmic brain networks
title Different computations over the same inputs produce selective behavior in algorithmic brain networks
title_full Different computations over the same inputs produce selective behavior in algorithmic brain networks
title_fullStr Different computations over the same inputs produce selective behavior in algorithmic brain networks
title_full_unstemmed Different computations over the same inputs produce selective behavior in algorithmic brain networks
title_short Different computations over the same inputs produce selective behavior in algorithmic brain networks
title_sort different computations over the same inputs produce selective behavior in algorithmic brain networks
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8853655/
https://www.ncbi.nlm.nih.gov/pubmed/35174783
http://dx.doi.org/10.7554/eLife.73651
work_keys_str_mv AT jaworskakatarzyna differentcomputationsoverthesameinputsproduceselectivebehaviorinalgorithmicbrainnetworks
AT yanyuening differentcomputationsoverthesameinputsproduceselectivebehaviorinalgorithmicbrainnetworks
AT vanrijsbergennicolaj differentcomputationsoverthesameinputsproduceselectivebehaviorinalgorithmicbrainnetworks
AT incerobinaa differentcomputationsoverthesameinputsproduceselectivebehaviorinalgorithmicbrainnetworks
AT schynsphilippeg differentcomputationsoverthesameinputsproduceselectivebehaviorinalgorithmicbrainnetworks