Michael Falkenstein

ERP components on reaction errors and their functional significance: a tutorial.

Some years ago we described a negative (Ne) and a later positive (Pe) deflection in the event-related brain potentials (ERPs) of incorrect choice reactions [Falkenstein, M., Hohnsbein, J., Hoormann, J., Blanke, L., 1990. In: Brunia, C.H.M., Gaillard, A.W.K., Kok, A. (Eds.), Psychophysiological Brain Research. Tilburg Univesity Press, Tilburg, pp. 192-195. Falkenstein, M., Hohnsbein, J., Hoormann, J., 1991. Electroencephalography and Clinical Neurophysiology, 78, 447-455]. Originally we assumed the Ne to represent a correlate of error detection in the sense of a mismatch signal when representations of the actual response and the required response are compared. This hypothesis was supported by the results of a variety of experiments from our own laboratory and that of Coles [Gehring, W. J., Goss, B., Coles, M.G.H., Meyer, D.E., Donchin, E., 1993. Psychological Science 4, 385-390. Bernstein, P.S., Scheffers, M.K., Coles, M.G.H., 1995. Journal of Experimental Psychology: Human Perception and Performance 21, 1312-1322. Scheffers, M.K., Coles, M. G.H., Bernstein, P., Gehring, W.J., Donchin, E., 1996. Psychophysiology 33, 42-54]. However, new data from our laboratory and that of Vidal et al. [Vidal, F., Hasbroucq, T., Bonnet, M., 1999. Biological Psychology, 2000] revealed a small negativity similar to the Ne also after correct responses. Since the above mentioned comparison process is also required after correct responses it is conceivable that the Ne reflects this comparison process itself rather than its outcome. As to the Pe, our results suggest that this is a further error-specific component, which is independent of the Ne, and hence associated with a later aspect of error processing or post-error processing. Our new results with different age groups argue against the hypotheses that the Pe reflects conscious error processing or the post-error adjustment of response strategies. Further research is necessary to specify the functional significance of the Pe.

Control and interference in task switching--a review.

The task-switching paradigm offers enormous possibilities to study cognitive control as well as task interference. The current review provides an overview of recent research on both topics. First, we review different experimental approaches to task switching, such as comparing mixed-task blocks with single-task blocks, predictable task-switching and task-cuing paradigms, intermittent instructions, and voluntary task selection. In the 2nd part, we discuss findings on preparatory control mechanisms in task switching and theoretical accounts of task preparation. We consider preparation processes in two-stage models, consider preparation as an all-or-none process, address the question of whether preparation is switch-specific, reflect on preparation as interaction of cue encoding and memory retrieval, and discuss the impact of verbal mediation on preparation. In the 3rd part, we turn to interference phenomena in task switching. We consider proactive interference of tasks and inhibition of recently performed tasks indicated by asymmetrical switch costs and n-2 task-repetition costs. We discuss stimulus-based interference as a result of stimulus-based response activation and stimulus-based task activation, and response-based interference because of applying bivalent rather than univalent responses, response repetition effects, and carryover of response selection and execution. In the 4th and final part, we mention possible future research fields.

Electroencephalography of response inhibition tasks: Functional networks and cognitive contributions

Response inhibition paradigms, as for example stop signal and go/no-go tasks, are often used to study cognitive control processes. Because of the apparent demand to stop a motor reaction, the electrophysiological responses evoked by stop and no-go trials have sometimes likewise been interpreted as indicators of inhibitory processes. Recent research, however, suggests a richer conceptual background. Evidence denotes an association of a frontal-midline N200/theta oscillations with premotor cognitive processes such as conflict monitoring or response program updating, and an anterior P300/delta oscillations with response-related, evaluative processing stages, probably the evaluation of motor inhibition. However, the data are still insufficient to unambiguously relate these electroencephalographic measures to specific inhibitory functions. Beta band activity only recently has become a focus of attention in this task context because of its association with the motor system and regions involved in inhibitory control. Its functional role in response inhibition tasks needs further exploration though. Hence, as things stand, any deduction of differences regarding actual inhibitory capabilities or loads between subject groups or conditions based on electroencephalographic measures has to be treated with caution.

Action monitoring, error detection, and the basal ganglia : an ERP study

The error negativity (Ne or ERN) is an event-related brain potential component, which is assumed to reflect error detection. Recently it has been hypothesized that the basal ganglia are assumed to play a crucial role in error detection. In the present study we ask whether the Ne is altered in patients with Parkinsons disease (PD), who have an impaired function of the basal ganglia. We recorded the Ne in patients and in matched controls, while they performed different tasks that require a relatively high cognitive control, which is supposed to pose particular problems on PD. The Ne was in fact smaller in the patients than in the controls in all tasks. Our results suggest an impairment of error detection in PD for different types of demanding tasks. This supports the hypothesis that the basal ganglia do play an important role for error detection in action monitoring.

Late ERP components in visual and auditory Go/Nogo tasks

In an audio-visual Go/Nogo paradigm we studied whether the Go/Nogo difference, usually found in the time range of the visual N2, is also present after auditory stimuli, which bears on the common response inhibition hypothesis of this N2 effect. Moreover the possible presence and variation of P300 subcomponents were studied with the goal of clarifying the reasons for the commonly observed P300 topography changes between Go and Nogo trials. To disentangle possible P300 subcomponents we applied a crossmodal divided attention (DA) condition, in which the subcomponents are known to be separated after auditory stimuli in choice tasks. An N2 effect was found after visual but not after auditory stimuli, which is evidence against the response-inhibition hypothesis. After visual stimuli a positive complex (P400) was seen, whereas after auditory stimuli two dissociated components (P400 and P507) were found instead. The P507 had a parietal maximum for both Go and Nogo trials. It was larger and it peaked later in Go than in Nogo trials. The P400 showed topographic differences between Go and Nogo trials, which could be explained by the overlap of the two subcomponents. We assume that (i) both subcomponents have a stable topography across response type, and (ii) the first subcomponent is invariant with response type, whereas the second (which overlaps the first one) is larger and peaks later on Go than on Nogo trials.

Inhibition-Related ERP Components: Variation with Modality, Age, and Time-on-Task

Abstract In Go/Nogo tasks, the ERP after Nogo stimuli generally reveals a negativity (Nogo-)N2 and a subsequent positivity (Nogo-)P3 over fronto-central scalp regions. These components are probably related to different subprocesses serving response inhibition, namely, modality-specific and general inhibition, respectively. In the present study we investigate whether aging or prolonged work (“time-on-task”) have an effect on N2 and P3. Twelve young and 12 elderly subjects performed simple Go/Nogo tasks to visual or auditory letter stimuli. Reaction times were longer after visual than after auditory stimuli, and longer in the elderly than in the young. The ERP results reveal a slight impairment of modality-specific inhibition (N2) in the elderly after visual, but not after auditory, stimuli. General inhibition (P3) was delayed in the elderly for both modalities, as was Go-P3 and RT. Hence, it appears that the response slowing of the elderly is the result of a slowing of the decision process whether to respo...

Parallel systems of error processing in the brain.

Major neurophysiological principles of performance monitoring are not precisely known. It is a current debate in cognitive neuroscience if an error-detection neural system is involved in behavioral control and adaptation. Such a system should generate error-specific signals, but their existence is questioned by observations that correct and incorrect reactions may elicit similar neuroelectric potentials. A new approach based on a time-frequency decomposition of event-related brain potentials was applied to extract covert sub-components from the classical error-related negativity (Ne) and correct-response-related negativity (Nc) in humans. A unique error-specific sub-component from the delta (1.5-3.5 Hz) frequency band was revealed only for Ne, which was associated with error detection at the level of overall performance monitoring. A sub-component from the theta frequency band (4-8 Hz) was associated with motor response execution, but this sub-component also differentiated error from correct reactions indicating error detection at the level of movement monitoring. It is demonstrated that error-specific signals do exist in the brain. More importantly, error detection may occur in multiple functional systems operating in parallel at different levels of behavioral control.

The Correction of Eye Blink Artefacts in the EEG: A Comparison of Two Prominent Methods

Background The study investigated the residual impact of eyeblinks on the electroencephalogram (EEG) after application of different correction procedures, namely a regression method (eye movement correction procedure, EMCP) and a component based method (Independent Component Analysis, ICA). Methodology/Principle Findings Real and simulated data were investigated with respect to blink-related potentials and the residual mutual information of uncorrected vertical electrooculogram (EOG) and corrected EEG, which is a measure of residual EOG contribution to the EEG. The results reveal an occipital positivity that peaks at about 250ms after the maximum blink excursion following application of either correction procedure. This positivity was not observable in the simulated data. Mutual information of vertical EOG and EEG depended on the applied regression procedure. In addition, different correction results were obtained for real and simulated data. ICA yielded almost perfect correction in all conditions. However, under certain conditions EMCP yielded comparable results to the ICA approach. Conclusion In conclusion, for EMCP the quality of correction depended on the EMCP variant used and the structure of the data, whereas ICA always yielded almost perfect correction. However, its disadvantage is the much more complex data processing, and that it requires a suitable amount of data.

ERP—Correlates of response selection in a response conflict paradigm

Neuroimaging and electrophysiological studies suggest that the anterior cingulate cortex (ACC) is involved in the cognitive control of response related action. A frontocentral negative ERP-component, the N2, which probably originates from the ACC, is usually enhanced in conflict-trials that demand an unexpected response. We here used stepped adjustment of response expectation in a response-cueing task, and measured how the N2 varied with global and local cue validity. Results showed that, irrespective of the current cue validity, response times, error rates, and the frontocentral components P2, N2 and P3 increased in unexpected trials. Nevertheless, a N2 was also seen in expected trials, and its latency correlated positively with reaction times, indicating that this potential does not express response conflict only. In line with roles suggested for the ACC, we here propose that the N2 is related to the process of response selection which influences subsequent processing stages reflected in the P3. Unexpected revisions of response programs enhance and delay the N2.

Short-term mobilization of processing resources is revealed in the event-related potential

This study investigates whether an occasional effortful improvement of performance, as asked for by a precue, is reflected in event-related potential (ERP) changes. To estimate the limits of possible effort-induced behavioral and ERP changes, we manipulated the time between precue and imperative stimulus (IS; precue interval, PCI). The subjects could, in fact, improve their performance in the effort trials, with all but the shortest PCI. The postcue ERP revealed a fronto-central contingent negative variation (CNV), which was preceded by a frontal positive/occipital negative wave (P2/N2). Both the P2/N2 and the CNV were larger for effort than for standard trials for all PCIs. For the shortest PCI (300 ms), the CNV increase was seen after the IS. The CNV increase for PCIs 600 and 300 began at about 400 ms postcue. The results suggest that effortful performance improvement is associated with prior increase of a frontocentral CNV and a preceding P2/N2. The CNV increase is thought to reflect the activity of a frontal executive process by which additional processing resources can be mobilized on a trial-to-trial basis within less than 500 ms.