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R Simson

Publications and source records attributed to R Simson.

24 records · Page 2Linked to original sources

The scalp topography of potentials in auditory and visual discrimination tasks.

Averaged event-related cortical potentials (ERPs) were obtained from an array of scalp electrodes overlying the left hemicranium in response to regularly presented visual or auditory stimuli (non-signals)and to infrequent random replacements by different stimuli (signals) in the same modality. A motor response was required to the signals. Non-signal ERPs were subtracted from signal ERPs and the topographic distributions of the negative (N2 delta) and positive (P3 delta) components were plotted as isopotential maps. N2 delta distributions differed for the auditory and visual modalities, whereas P3delta was modality unspecific. These topographic data were compared to those from the previous study of missing stimulus potentials (Simson et al. 1976) using maps representing the contributions from unilateral cerebral sources. The N2 delta and negative missing stimulus potential distributions ascribed to cortical activity within the secondary auditory and visual regions, whereas the late positive component (positive missing stimulus potential or P3 delta) were considered to derive principally from inferior parietal association cortex.

Adult↗

The scalp topography of potentials associated with missing visual or auditory stimuli.

Averaged potentials time-locked to regularly presented visual and auditory stimuli and to the occasional random deletion of a stimulus were recorded from a scalp electrode array overlying the left hemicranium. The major components of visual and auditory evoked potentials and of the potentials associated with missing stimuli (MSP) were measured and their amplitude distributions depicted in the form of isopotential maps. The N1 components of the VEP and AEP had distributions compatible with sources in and near the respective primary cortical projection areas. The P2 components were more widely distributed and could be attributed in part to generators within modality specific association areas. The MSP comprised two main components, an initial negativity (NMSP) and a later positive wave (PMSP). The NMSP distributions were different in the visual and auditory modalities, and were similar to the respective EP topographies. The NMSP appeared to reflect a more powerful contribution of association areas than did the evoked responses. The PMSP topography was modality unspecific with distributions which were maximal over the parietal region. The possible functional significance of the NMSP and PMSP was considered in the light of their timing and topography.

Adult↗

Cortical evoked potentials elicited by real speech words and human sounds.

Averaged evoked potentials were recorded from PZ and left and right temporo-parietal electodes to real speech words and human sounds in 8 right-handed subjects. Stimuli were presented in a "no task" condition where the subject was instructed to listen attentively, and a vigilance condition where the subject responded to a particular word or sound during a run of such stimuli. The vigilance condition produced two classes of stimuli:signals and non-signals. Evoked potentials to physically identical words or sounds were examined when they were "no task", non-signal and signal stimuli. P300 amplitude increased significantly as a function of increasing task demands going from "no task" to non-signal to signal. When a strict statistical criterion for multiple comparisons (Bonferroni test) was applied in looking for asymmetries between hemispheres, only 2 isolated left greater than right differences turned out to be significant. Review of the literature concerning evoked potential correlates of differential hemispheric processing pointed up flaws in design, statistical technique, and inconsistencies in reported findings which suggested that while evoked potentials may sometimes reflect differences in hemispheric functioning, this effect is marginal at best.

Adult↗

The late positive component (P300) and information processing in sentences.

Averaged visual evoked potentials to sequentially flashed words comprising a sentence were recorded from vertex and left and right temporoparietal electrodes in 8 right-handed subjects. In condition 1 the sentence took the form: The -eel is on the shoe, in which the first grapheme was omitted from the second word, so that the subject did not know the meaning of the second word until he viewed the last word. In condition 2, the sentence took the form: The heel is on the shoe, in which the second word was given and the last word provided no further information. P300 latency to words which delivered information (last word of condition 1, second word of condition 2) were significantly longer than P300 latency to any of the other words in the sentence, as well as to the same position word in the other condition. Comparisons of P300 latencies to redundant words (the, is, on) within and between conditions showed no significant differences. P300 amplitude to the last word was significantly larger than P300 amplitude to any of the other words within the sentence, even in condition 2 where the second word delivered information. The major effect of information delivery was on P300 latency, while "syntactic closure" had its major effect on P300 amplitude. The fact that evoked potentials to all words had P300 components was attributed to the engagement of the P300 system whenever task-related language stimuli are used.

Adolescent↗

Evoked potentials in the assessment of neurotoxicity in humans.

The present paper reviews strengths and weaknesses of evoked potentials (EPs) as an index of toxic insult to the nervous system. EPs are obtained by averaging successive samples of EEG time-locked to the presentation of stimuli. Components of the resulting waveform can be measured for amplitude, latency, and distribution. Normal ranges of these parameters have been characterized for auditory, visual and somatosensory stimuli. Auditory EPs have been studied in humans exposed to lead, trichloroethylene, and carbon monoxide. Changes in timing of short latency components and in amplitude of later cortical components have been reported. Methyl mercury, n-hexane and carbon monoxide cause complex changes in the waveshape of flash and patterned visual EPs. Similarly, specific components of somatosensory EPs are altered following exposure to carbon monoxide, lead and acrylamide. The current lack of standardized recording and analysis techniques has sometimes generated contradictory results, but the evidence thus far supports the ultimate usefulness of EPs as a neurotoxicological screening tool.

Animals↗