Linguistic Structure and Meaning Organize Neural Oscillations into a Content-Specific Hierarchy
Neural oscillations track linguistic information during speech comprehension (Ding et al., 2016; Keitel et al., 2018), and are known to be modulated by acoustic landmarks and speech intelligibility (Doelling et al., 2014; Zoefel and VanRullen, 2015). However, studies investigating linguistic trackin...
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description | Neural oscillations track linguistic information during speech comprehension (Ding et al., 2016; Keitel et al., 2018), and are known to be modulated by acoustic landmarks and speech intelligibility (Doelling et al., 2014; Zoefel and VanRullen, 2015). However, studies investigating linguistic tracking have either relied on non-naturalistic isochronous stimuli or failed to fully control for prosody. Therefore, it is still unclear whether low-frequency activity tracks linguistic structure during natural speech, where linguistic structure does not follow such a palpable temporal pattern. Here, we measured electroencephalography (EEG) and manipulated the presence of semantic and syntactic information apart from the timescale of their occurrence, while carefully controlling for the acoustic-prosodic and lexical-semantic information in the signal. EEG was recorded while 29 adult native speakers (22 women, 7 men) listened to naturally spoken Dutch sentences, jabberwocky controls with morphemes and sentential prosody, word lists with lexical content but no phrase structure, and backward acoustically matched controls. Mutual information (MI) analysis revealed sensitivity to linguistic content: MI was highest for sentences at the phrasal (0.8-1.1 Hz) and lexical (1.9-2.8 Hz) timescales, suggesting that the delta-band is modulated by lexically driven combinatorial processing beyond prosody, and that linguistic content (i.e., structure and meaning) organizes neural oscillations beyond the timescale and rhythmicity of the stimulus. This pattern is consistent with neurophysiologically inspired models of language comprehension (Martin, 2016, 2020; Martin and Doumas, 2017) where oscillations encode endogenously generated linguistic content over and above exogenous or stimulus-driven timing and rhythm information.
Biological systems like the brain encode their environment not only by reacting in a series of stimulus-driven responses, but by combining stimulus-driven information with endogenous, internally generated, inferential knowledge and meaning. Understanding language from speech is the human benchmark for this. Much research focuses on the purely stimulus-driven response, but here, we focus on the goal of language behavior: conveying structure and meaning. To that end, we use naturalistic stimuli that contrast acoustic-prosodic and lexical-semantic information to show that, during spoken language comprehension, oscillatory modulations reflect computations related to i |
doi_str_mv | 10.1523/JNEUROSCI.0302-20.2020 |
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Biological systems like the brain encode their environment not only by reacting in a series of stimulus-driven responses, but by combining stimulus-driven information with endogenous, internally generated, inferential knowledge and meaning. Understanding language from speech is the human benchmark for this. Much research focuses on the purely stimulus-driven response, but here, we focus on the goal of language behavior: conveying structure and meaning. To that end, we use naturalistic stimuli that contrast acoustic-prosodic and lexical-semantic information to show that, during spoken language comprehension, oscillatory modulations reflect computations related to inferring structure and meaning from the acoustic signal. Our experiment provides the first evidence to date that compositional structure and meaning organize the oscillatory response, above and beyond prosodic and lexical controls.</description><identifier>ISSN: 0270-6474</identifier><identifier>EISSN: 1529-2401</identifier><identifier>DOI: 10.1523/JNEUROSCI.0302-20.2020</identifier><identifier>PMID: 33097640</identifier><language>eng</language><publisher>United States: Society for Neuroscience</publisher><subject>Acoustic Stimulation ; Acoustics ; Adult ; Combinatorial analysis ; Comprehension ; Comprehension - physiology ; Delta Rhythm - physiology ; Dutch language ; EEG ; Electroencephalography ; Female ; Humans ; Intelligibility ; Lexical semantics ; Linguistics ; Male ; Mental Processes - physiology ; Morphemes ; Oscillations ; Phrase structure ; Prosody ; Psycholinguistics ; Rhythm ; Semantics ; Sentences ; Speech ; Speech Perception ; Syntax ; Time ; Word lists ; Young Adult</subject><ispartof>The Journal of neuroscience, 2020-12, Vol.40 (49), p.9467-9475</ispartof><rights>Copyright © 2020 the authors.</rights><rights>Copyright Society for Neuroscience Dec 2, 2020</rights><rights>Copyright © 2020 the authors 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-ceafb8fd6cc70f6e4320fe73ea8d435c65151073cd70eab9bc14dcef6484bea13</citedby><cites>FETCH-LOGICAL-c442t-ceafb8fd6cc70f6e4320fe73ea8d435c65151073cd70eab9bc14dcef6484bea13</cites><orcidid>0000-0002-9984-5745 ; 0000-0003-0470-442X ; 0000-0001-7547-5842 ; 0000-0002-3395-7234 ; 0000-0002-2628-7738</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7724143/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7724143/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33097640$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kaufeld, Greta</creatorcontrib><creatorcontrib>Bosker, Hans Rutger</creatorcontrib><creatorcontrib>Ten Oever, Sanne</creatorcontrib><creatorcontrib>Alday, Phillip M</creatorcontrib><creatorcontrib>Meyer, Antje S</creatorcontrib><creatorcontrib>Martin, Andrea E</creatorcontrib><title>Linguistic Structure and Meaning Organize Neural Oscillations into a Content-Specific Hierarchy</title><title>The Journal of neuroscience</title><addtitle>J Neurosci</addtitle><description>Neural oscillations track linguistic information during speech comprehension (Ding et al., 2016; Keitel et al., 2018), and are known to be modulated by acoustic landmarks and speech intelligibility (Doelling et al., 2014; Zoefel and VanRullen, 2015). However, studies investigating linguistic tracking have either relied on non-naturalistic isochronous stimuli or failed to fully control for prosody. Therefore, it is still unclear whether low-frequency activity tracks linguistic structure during natural speech, where linguistic structure does not follow such a palpable temporal pattern. Here, we measured electroencephalography (EEG) and manipulated the presence of semantic and syntactic information apart from the timescale of their occurrence, while carefully controlling for the acoustic-prosodic and lexical-semantic information in the signal. EEG was recorded while 29 adult native speakers (22 women, 7 men) listened to naturally spoken Dutch sentences, jabberwocky controls with morphemes and sentential prosody, word lists with lexical content but no phrase structure, and backward acoustically matched controls. Mutual information (MI) analysis revealed sensitivity to linguistic content: MI was highest for sentences at the phrasal (0.8-1.1 Hz) and lexical (1.9-2.8 Hz) timescales, suggesting that the delta-band is modulated by lexically driven combinatorial processing beyond prosody, and that linguistic content (i.e., structure and meaning) organizes neural oscillations beyond the timescale and rhythmicity of the stimulus. This pattern is consistent with neurophysiologically inspired models of language comprehension (Martin, 2016, 2020; Martin and Doumas, 2017) where oscillations encode endogenously generated linguistic content over and above exogenous or stimulus-driven timing and rhythm information.
Biological systems like the brain encode their environment not only by reacting in a series of stimulus-driven responses, but by combining stimulus-driven information with endogenous, internally generated, inferential knowledge and meaning. Understanding language from speech is the human benchmark for this. Much research focuses on the purely stimulus-driven response, but here, we focus on the goal of language behavior: conveying structure and meaning. To that end, we use naturalistic stimuli that contrast acoustic-prosodic and lexical-semantic information to show that, during spoken language comprehension, oscillatory modulations reflect computations related to inferring structure and meaning from the acoustic signal. Our experiment provides the first evidence to date that compositional structure and meaning organize the oscillatory response, above and beyond prosodic and lexical controls.</description><subject>Acoustic Stimulation</subject><subject>Acoustics</subject><subject>Adult</subject><subject>Combinatorial analysis</subject><subject>Comprehension</subject><subject>Comprehension - physiology</subject><subject>Delta Rhythm - physiology</subject><subject>Dutch language</subject><subject>EEG</subject><subject>Electroencephalography</subject><subject>Female</subject><subject>Humans</subject><subject>Intelligibility</subject><subject>Lexical semantics</subject><subject>Linguistics</subject><subject>Male</subject><subject>Mental Processes - physiology</subject><subject>Morphemes</subject><subject>Oscillations</subject><subject>Phrase structure</subject><subject>Prosody</subject><subject>Psycholinguistics</subject><subject>Rhythm</subject><subject>Semantics</subject><subject>Sentences</subject><subject>Speech</subject><subject>Speech Perception</subject><subject>Syntax</subject><subject>Time</subject><subject>Word lists</subject><subject>Young Adult</subject><issn>0270-6474</issn><issn>1529-2401</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkU9rGzEQxUVJaRy3XyEIcsll3dGfXdmXQDBJk-LGUDdnodXOOgq25EjaQPrpI5PUtD3NwHvzmMePkFMGE1Zz8fX73dX9z-VqfjsBAbziMOHA4QMZFXVWcQnsiIyAK6gaqeQxOUnpEQAUMPWJHAsBM9VIGBG9cH49uJSdpascB5uHiNT4jv5A44tGl3Fdlt9I73CIZkOXybrNxmQXfKLO50ANnQef0edqtUPr-hJ14zCaaB9ePpOPvdkk_PI-x-T--urX_KZaLL_dzi8XlZWS58qi6dtp3zXWKugblIJDj0qgmXZS1LapWc1ACdspQNPOWstkZ7Fv5FS2aJgYk4u33N3QbrFIPpdn9S66rYkvOhin_1W8e9Dr8KyV4pJJUQLO3wNieBowZb11yWJp6jEMSXNZS8ZEI-tiPfvP-hiG6Eu94lJSQL1PHJPmzWVjSClif3iGgd4z1AeGes9Qc9B7huXw9O8qh7M_0MQrjFibOA</recordid><startdate>20201202</startdate><enddate>20201202</enddate><creator>Kaufeld, Greta</creator><creator>Bosker, Hans Rutger</creator><creator>Ten Oever, Sanne</creator><creator>Alday, Phillip M</creator><creator>Meyer, Antje S</creator><creator>Martin, Andrea E</creator><general>Society for Neuroscience</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7QR</scope><scope>7T9</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-9984-5745</orcidid><orcidid>https://orcid.org/0000-0003-0470-442X</orcidid><orcidid>https://orcid.org/0000-0001-7547-5842</orcidid><orcidid>https://orcid.org/0000-0002-3395-7234</orcidid><orcidid>https://orcid.org/0000-0002-2628-7738</orcidid></search><sort><creationdate>20201202</creationdate><title>Linguistic Structure and Meaning Organize Neural Oscillations into a Content-Specific Hierarchy</title><author>Kaufeld, Greta ; 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Keitel et al., 2018), and are known to be modulated by acoustic landmarks and speech intelligibility (Doelling et al., 2014; Zoefel and VanRullen, 2015). However, studies investigating linguistic tracking have either relied on non-naturalistic isochronous stimuli or failed to fully control for prosody. Therefore, it is still unclear whether low-frequency activity tracks linguistic structure during natural speech, where linguistic structure does not follow such a palpable temporal pattern. Here, we measured electroencephalography (EEG) and manipulated the presence of semantic and syntactic information apart from the timescale of their occurrence, while carefully controlling for the acoustic-prosodic and lexical-semantic information in the signal. EEG was recorded while 29 adult native speakers (22 women, 7 men) listened to naturally spoken Dutch sentences, jabberwocky controls with morphemes and sentential prosody, word lists with lexical content but no phrase structure, and backward acoustically matched controls. Mutual information (MI) analysis revealed sensitivity to linguistic content: MI was highest for sentences at the phrasal (0.8-1.1 Hz) and lexical (1.9-2.8 Hz) timescales, suggesting that the delta-band is modulated by lexically driven combinatorial processing beyond prosody, and that linguistic content (i.e., structure and meaning) organizes neural oscillations beyond the timescale and rhythmicity of the stimulus. This pattern is consistent with neurophysiologically inspired models of language comprehension (Martin, 2016, 2020; Martin and Doumas, 2017) where oscillations encode endogenously generated linguistic content over and above exogenous or stimulus-driven timing and rhythm information.
Biological systems like the brain encode their environment not only by reacting in a series of stimulus-driven responses, but by combining stimulus-driven information with endogenous, internally generated, inferential knowledge and meaning. Understanding language from speech is the human benchmark for this. Much research focuses on the purely stimulus-driven response, but here, we focus on the goal of language behavior: conveying structure and meaning. To that end, we use naturalistic stimuli that contrast acoustic-prosodic and lexical-semantic information to show that, during spoken language comprehension, oscillatory modulations reflect computations related to inferring structure and meaning from the acoustic signal. Our experiment provides the first evidence to date that compositional structure and meaning organize the oscillatory response, above and beyond prosodic and lexical controls.</abstract><cop>United States</cop><pub>Society for Neuroscience</pub><pmid>33097640</pmid><doi>10.1523/JNEUROSCI.0302-20.2020</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-9984-5745</orcidid><orcidid>https://orcid.org/0000-0003-0470-442X</orcidid><orcidid>https://orcid.org/0000-0001-7547-5842</orcidid><orcidid>https://orcid.org/0000-0002-3395-7234</orcidid><orcidid>https://orcid.org/0000-0002-2628-7738</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acoustic Stimulation Acoustics Adult Combinatorial analysis Comprehension Comprehension - physiology Delta Rhythm - physiology Dutch language EEG Electroencephalography Female Humans Intelligibility Lexical semantics Linguistics Male Mental Processes - physiology Morphemes Oscillations Phrase structure Prosody Psycholinguistics Rhythm Semantics Sentences Speech Speech Perception Syntax Time Word lists Young Adult |
title | Linguistic Structure and Meaning Organize Neural Oscillations into a Content-Specific Hierarchy |
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