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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
11

The Brain Differentially Prepares Inner and Overt Speech Production: Electrophysiological and Vascular Evidence

Stephan, Franziska, Saalbach, Henrik, Rossi, Sonja 13 April 2023 (has links)
Speech production not only relies on spoken (overt speech) but also on silent output (inner speech). Little is known about whether inner and overt speech are processed differently and which neural mechanisms are involved. By simultaneously applying electroencephalography (EEG) and functional near-infrared spectroscopy (fNIRS), we tried to disentangle executive control from motor and linguistic processes. A preparation phase was introduced additionally to the examination of overt and inner speech directly during naming (i.e., speech execution). Participants completed a picture-naming paradigm in which the pure preparation phase of a subsequent speech production and the actual speech execution phase could be differentiated. fNIRS results revealed a larger activation for overt rather than inner speech at bilateral prefrontal to parietal regions during the preparation and at bilateral temporal regions during the execution phase. EEG results showed a larger negativity for inner compared to overt speech between 200 and 500 ms during the preparation phase and between 300 and 500 ms during the execution phase. Findings of the preparation phase indicated that differences between inner and overt speech are not exclusively driven by specific linguistic and motor processes but also impacted by inhibitory mechanisms. Results of the execution phase suggest that inhibitory processes operate during phonological code retrieval and encoding.
12

Inner versus Overt Speech Production: Does This Make a Difference in the Developing Brain?

Stephan, Franzisk, Saalbach, Henrik, Rossi, Sonja 13 April 2023 (has links)
Studies in adults showed differential neural processing between overt and inner speech. So far, it is unclear whether inner and overt speech are processed differentially in children. The present study examines the pre-activation of the speech network in order to disentangle domain-general executive control from linguistic control of inner and overt speech production in 6- to 7-year-olds by simultaneously applying electroencephalography (EEG) and functional near-infrared spectroscopy (fNIRS). Children underwent a picture-naming task in which the pure preparation of a subsequent speech production and the actual execution of speech can be differentiated. The preparation phase does not represent speech per se but it resembles the setting up of the language production network. Only the fNIRS revealed a larger activation for overt, compared to inner, speech over bilateral prefrontal to parietal regions during the preparation phase. Findings suggest that the children’s brain can prepare the subsequent speech production. The preparation for overt and inner speech requires different domain-general executive control. In contrast to adults, the children’s brain did not show differences between inner and overt speech when a concrete linguistic content occurs and a concrete execution is required. This might indicate that domain-specific executive control processes are still under development.
13

Propagation de l’activation entre le lexique orthographique et le système affectif / Activation spread between the orthographic lexicon and the affective system in visual word recognition

Gobin, Paméla 27 September 2011 (has links)
L’objectif de cette thèse est d’étudier l’activation du système affectif médiée par le lexique orthographique au cours de la reconnaissance visuelle des mots. Plus précisément, nous avons étudié l’influence du voisinage orthographique émotionnel négatif et la sensibilité de l’amorçage orthographique à la valence négative de voisins plus fréquents dans une tâche de décision lexicale (TDL) combinée à un paradigme d’amorçage. Le recueil de mesures comportementales et électrophysiologiques (potentiels évoqués) nous a également permis d’évaluer la précocité de l’activation des composantes émotionnelles des voisins. Des mots neutres (e.g., FUSEAU, TOISON) ayant un seul voisin orthographique plus fréquent neutre (e.g., museau) ou négatif (e.g., poison) ont ainsi été présentés dans la TDL. Ils étaient précédés de leur voisin ou d’une amorce contrôle non alphabétique présenté pendant 66 ou 166 ms. Dans un premier temps, l’état émotionnel des participants a été contrôlé (Expériences 1-4). Dans un second temps, il a été manipulé a priori par une induction d’humeur triste (Expériences 5 et 7) ou déterminé a posteriori en considérant le niveau d’épuisement professionnel des participants (Expériences 7-8). Le traitement des mots fréquents neutres ou négatifs a été examiné en complément (Expérience 6). Les résultats montrent un effet inhibiteur du voisinage orthographique émotionnel négatif sur les temps de reconnaissance des mots cibles ainsi qu’un effet inhibiteur d’amorçage orthographique, accru par la durée de présentation des amorces. Trois composantes (P150, N200 et N400) constituent les corrélats électrophysiologiques de l’effet d’amorçage orthographique, sensibles à la valence négative des voisins et à la durée de présentation des amorces. Enfin, l’état émotionnel des individus modifie l’effet d’amorçage orthographique. Les résultats sont interprétés dans un modèle de type Activation Interactive de reconnaissance visuelle des mots adapté aux traitements affectifs. / The aim of this thesis was to study the activation of the affective system mediated by the orthographic lexicon during visual word recognition. More precisely, we have investigated the influence of the negative emotional orthographic neighbourhood and the sensitivity of orthographic priming to the negative valence of higher-frequency neighbours in the lexical decision task (LDT) combined with a priming paradigm. The recording of behavioural and electrophysiological (event-related brain potentials) measures provides also evidences on the early activation of affective components of the neighbours. Neutral words (e.g., FUSEAU [spindle], TOISON [fleece]) with one higher-frequency neighbour, that was either neutral (e.g., museau [muzzle]) or negative (e.g., poison), were presented in the LDT. They were preceded either by their neighbour or by a nonalphabetic control prime, presented 66 or 166 ms. Firstly, the emotional state of participants was controlled (Experiments 1-4). Secondly, it was manipulated a priori by a sad mood induction (Experiments 5 and 7) or determined a posteriori by considering the burnout level of participants (Experiments 7-8). The processing of negative or neutral frequent words have been also examined (Experiment 6). The results showed an inhibitory effect of negative emotional orthographic neighbourhood on target recognition time and an inhibitory effect of orthographic priming, increased by prime duration. Three components (P150, N200, and N400) were the electrophysiological correlates of orthographic priming effect, also depending on the negative valence of higher-frequency neighbours and prime duration. Finally, the emotional state of individuals modified the orthographic priming effect. The results are interpreted in an Interactive Activation model extended to affective processing.
14

Genetics, drugs, and cognitive control: uncovering individual differences in substance dependence

Baker, Travis Edward 11 September 2012 (has links)
Why is it that only some people who use drugs actually become addicted? In fact, addiction depends on a complicated process involving a confluence of risk factors related to biology, cognition, behaviour, and personality. Notably, all addictive drugs act on a neural system for reinforcement learning called the midbrain dopamine system, which projects to and regulates the brain's system for cognitive control, called frontal cortex and basal ganglia. Further, the development and expression of the dopamine system is determined in part by genetic factors that vary across individuals such that dopamine related genes are partly responsible for addiction-proneness. Taken together, these observations suggest that the cognitive and behavioral impairments associated with substance abuse result from the impact of disrupted dopamine signals on frontal brain areas involved in cognitive control: By acting on the abnormal reinforcement learning system of the genetically vulnerable, addictive drugs hijack the control system to reinforce maladaptive drug-taking behaviors. The goal of this research was to investigate this hypothesis by conducting a series of experiments that assayed the integrity of the dopamine system and its neural targets involved in cognitive control and decision making in young adults using a combination of electrophysiological, behavioral, and genetic assays together with surveys of substance use and personality. First, this research demonstrated that substance dependent individuals produce an abnormal Reward-positivity, an electrophysiological measure of a cortical mechanism for dopamine-dependent reward processing and cognitive control, and behaved abnormally on a decision making task that is diagnostic of dopamine dysfunction. Second, several dopamine-related neural pathways underlying individual differences in substance dependence were identified and modeled, providing a theoretical framework for bridging the gap between genes and behavior in drug addiction. Third, the neural mechanisms that underlie individual differences in decision making function and dysfunction were identified, revealing possible risk factors in the decision making system. In sum, these results illustrate how future interventions might be individually tailored for specific genetic, cognitive and personality profiles. / Graduate
15

Signs in the brain: Hearing signers’ cross-linguistic semantic integration strategies

Zachau, S. (Swantje) 28 September 2016 (has links)
Abstract Audio-oral speech and visuo-manual sign language as used by the Deaf community are two very different realizations of the human linguistic communication system. Sign language is not only used by the hearing impaired but also by different groups of hearing individuals. To date, there is a great discrepancy in scientific knowledge about signed and spoken languages. Particularly little is known about the integration of the two systems, even though the vast majority of deaf and hearing signers also have a command of some form of speech. This neurolinguistic study aimed to achieve basic knowledge about semantic integration mechanisms across speech and sign language in hearing native and non-native signers. Basic principles of sign processing as reflected in electrocortical brain activation and behavioral decisions were examined in three groups of study participants: Hearing native signers (children of deaf adults, CODAs), hearing late learned signers (professional sign language interpreters), and hearing non-signing controls. Event-related brain potentials (ERPs) and behavioral response frequencies were recorded while the participants performed a semantic decision task for priming lexeme pairs. The lexeme pairs were presented either within speech (spoken prime-spoken target) or across speech and sign language (spoken prime-signed target). Target-related ERP responses were subjected to temporal principal component analyses (tPCA). The neurocognitive basis of semantic integration processes were assessed by analyzing different ERP components (N170, N400, late positive complex) in response to the antonymic and unrelated targets. Behavioral decision sensitivity to the target lexemes is discussed in relation to the measured brain activity. Behaviorally, all three groups of study participants performed above chance level when making semantic decisions about the primed targets. Different result patterns, however, hinted at three different processing strategies. As the target-locked electrophysiological data was analyzed by PCA, for the first time in the context of sign language processing, objectively allocated ERP components of interest could be explored. A little surprisingly, the overall study results from the sign-naïve control group showed that they performed in a more content-guided way than expected. This suggested that even non-experts in the field of sign language were equipped with basic skills to process the cross-linguistically primed signs. Behavioral and electrophysiological study results together further brought up qualitative differences in processing between the native and late learned signers, which raised the question: can a unitary model of sign processing do justice to different groups of sign language users? / Tiivistelmä Kuuloaistiin ja ääntöelimistön motoriikkaan perustuva puhe ja kuurojen yhteisön käyttämä, näköaistiin ja käsien liikkeisiin perustuva viittomakieli ovat kaksi varsin erilaista ihmisen kielellisen viestintäjärjestelmän toteutumismuotoa. Viittomakieltä käyttävät kuulovammaisten ohella myös monet kuulevat ihmisryhmät. Tähänastinen tutkimustiedon määrä viittomakielistä ja puhutuista kielistä eroaa huomattavasti. Erityisen vähän on tiedetty näiden kahden järjestelmän yhdistämisestä, vaikka valtaosa kuuroista ja kuulevista viittomakielen käyttäjistä hallitsee myös puheen jossain muodossa. Tämän neurolingvistisen tutkimuksen tarkoituksena oli hankkia perustietoja puheen ja viittomakielen välisistä semanttisista yhdistämismekanismeista kuulevilla, viittomakieltä äidinkielenään tai muuna kielenä käyttävillä henkilöillä. Viittomien prosessoinnin perusperiaatteita, jotka ilmenevät aivojen sähköisen toiminnan muutoksina ja valintapäätöksinä, tutkittiin kolmessa koehenkilöryhmässä: kuulevilla viittomakieltä äidinkielenään käyttävillä henkilöillä (kuurojen aikuisten kuulevilla ns. CODA-lapsilla, engl. children of deaf adults), kuulevilla viittomakielen myöhemmin oppineilla henkilöillä (viittomakielen ammattitulkeilla) sekä kuulevilla viittomakieltä osaamattomilla verrokkihenkilöillä. Tapahtumasidonnaiset herätepotentiaalit (ERP:t) ja käyttäytymisvasteen frekvenssit rekisteröitiin koehenkilöiden tehdessä semanttisia valintoja viritetyistä (engl. primed) lekseemipareista. Lekseemiparit esitettiin joko puheena (puhuttu viritesana – puhuttu kohdesana) tai puheen ja viittomakielen välillä (puhuttu viritesana – viitottu kohdesana). Kohdesidonnaisille ERP-vasteille tehtiin temporaaliset pääkomponenttianalyysit (tPCA). Semanttisten yhdistämisprosessien neurokognitiivista perustaa arvioitiin analysoimalla erilaisia ERP-komponentteja (N170, N400, myöhäinen positiivinen kompleksi) vastineina antonyymisiin ja toisiinsa liittymättömiin kohteisiin. Käyttäytymispäätöksen herkkyyttä kohdelekseemeille tarkastellaan suhteessa mitattuun aivojen aktiviteettiin. Käyttäytymisen osalta kaikki kolme koehenkilöryhmää suoriutuivat satunnaistasoa paremmin tehdessään semanttisia valintoja viritetyistä kohdelekseemeistä. Erilaiset tulosmallit viittaavat kuitenkin kolmeen erilaiseen prosessointistrategiaan. Kun kohdelukittua elektrofysiologista dataa analysoitiin pääkomponenttianalyysin avulla ensimmäistä kertaa viittomakielen prosessoinnin yhteydessä, voitiin tutkia tarkkaavaisuuden objektiivisesti allokoituja ERP-komponentteja. Oli jossain määrin yllättävää, että viittomakielellisesti natiivin verrokkiryhmän tulokset osoittivat sen jäsenten toimivan odotettua sisältölähtöisemmin. Tämä viittaa siihen, että viittomakieleen perehtymättömilläkin henkilöillä on perustaidot lingvistisesti ristiin viritettyjen viittomien prosessointiin. Yhdessä käyttäytymisperäiset ja elektrofysiologiset tutkimustulokset toivat esiin laadullisia eroja prosessoinnissa viittomakieltä äidinkielenään puhuvien henkilöiden ja kielen myöhemmin oppineiden henkilöiden välillä. Tämä puolestaan johtaa kysymykseen, voiko yksi viittomien prosessointimalli soveltua erilaisille viittomakielen käyttäjäryhmille?

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