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Age of acquisition (AOA) is a psycholinguistic variable that significantly influences behavioural measures (response times and accuracy rates) in tasks that require lexical and semantic processing. Its origin is – unlike the origin of semantic typicality (TYP), which is assumed at the semantic level – controversially discussed. Different theories propose AOA effects to originate either at the semantic level or at the link between semantics and phonology (lemma-level).
The dissertation aims at investigating the influence of AOA and its interdependence with the semantic variable TYP on particularly semantic processing in order to pinpoint the origin of AOA effects. Therefore, three studies have been conducted that considered the variables AOA and TYP in semantic processing tasks (category verifications and animacy decisions) by means of behavioural and partly electrophysiological (ERP) data and in different populations (healthy young and elderly participants and in semantically impaired individuals with aphasia (IWA)).
The behavioural and electrophysiological data of the three studies provide evidence for distinct processing levels of the variables AOA and TYP. The data further support previous assumptions on a semantic origin for TYP but question the same for AOA. The findings, however, support an origin of AOA effects at the transition between the word form (phonology) and the semantic level that can be captured at the behavioural but not at the electrophysiological level.
Infants as young as six months are sensitive to prosodic phrase boundaries marked by three acoustic cues: pitch change, final lengthening, and pause. Behavioral studies suggest that a language-specific weighting of these cues develops during the first year of life; recent work on German revealed that eight-month-olds, unlike six-month-olds, are capable of perceiving a prosodic boundary on the basis of pitch change and final lengthening only. The present study uses Event-Related Potentials (ERPs) to investigate the neuro-cognitive development of prosodic cue perception in German-learning infants. In adults’ ERPs, prosodic boundary perception is clearly reflected by the so-called Closure Positive Shift (CPS). To date, there is mixed evidence on whether an infant CPS exists that signals early prosodic cue perception, or whether the CPS emerges only later—the latter implying that infantile brain responses to prosodic boundaries reflect acoustic, low-level pause detection.
We presented six- and eight-month-olds with stimuli containing either no boundary cues, only a pitch cue, or a combination of both pitch change and final lengthening. For both age groups, responses to the former two conditions did not differ, while brain responses to prosodic boundaries cued by pitch change and final lengthening showed a positivity that we interpret as a CPS-like infant ERP component. This hints at an early sensitivity to prosodic boundaries that cannot exclusively be based on pause detection. Instead, infants’ brain responses indicate an early ability to exploit subtle, relational prosodic cues in speech perception—presumably even earlier than could be concluded from previous behavioral results.
Individuals differ in the time needed to name a picture. This contribution asks whether this inter-individual variability emerges in earlier stages of word production (e.g. lexical selection) or later stages (e.g. articulation) and examines the consequences of this variability for EEG group results. We measured participants' (N = 45) naming latencies and continuous EEG in a picture-word interference task and naming latencies in a delayed naming task. Inter-individual variability in naming latencies in immediate naming (in contrast with inter-item variability) was not larger than the variability in the delayed task, suggesting that some variability in immediate naming originates in later stages of word production. EEG data complemented this interpretation: Differences between relatively fast vs. slow speakers emerged in response-aligned analyses in a time window close to the vocal response. We additionally present a method to assess the generalisability of the timing of effects across participants based on random sampling.