We employed an adaptation of the Simon task during recordings of MEG (Simon JR, Small AM. Processing auditory information: Interference from an irrelevant cue. J Appl Psychol. 1969;53: 433–435. doi:10.1037/h0028034). We provide a neuromagnetic datasets recorded using a whole-head magenetoencephalography system from 4D Neuroimaging (MAGNES®-3600WH MEG). The dataset consists of continuous neuromagnetic activity from regions of interests. For this the MEG data were continuously recorded with a sampling rate of 678.17 Hz and a bandwidth of 0 to 200 Hz. Environmental and power line noise as well as signal contributions due to eye movements or cardiac activity was removed from the data. The dynamics of predefined region of interests (ROI)are extracted on which Granger causality was applied to investigate the interconnections between the active brain regions, as well as their directionality. The dataset can be exploited to address crucial issues in neurophysiology such as: 1) What are the underlying neural mechanisms of the fronto-parietal attention network (FPAN). 2) What are the principles of neural interactions and 3) What are the temporal characteristics and directional interconnections. It has been reported that the network is influenced by ageing and appears to be associated with mental illnesses such as schizophrenia and attention-deficit hyperactivity disorder.
The suppression of distracting information in order to focus on an actual cognitive goal is a key feature of executive functions. The use of brain imaging methods to investigate the underlying neurobiological brain activations that occur during conflict processing have demonstrated the strong involvement of the fronto-parietal attention network (FPAN). Surprisingly, the directional interconnections, their time courses and activations at different frequency bands remain to be elucidated, and thus, this constitutes the focus of this study. We employed an adaptation of the Simon task during Magneto¬encephalography (MEG). Granger causality was applied to investigate the interconnections between the active brain regions, as well as their directionality. Following stimulus onset, the middle frontal precentral cortex and superior parietal cortex were significantly activated during conflict processing in a time window of between 300 and 600ms. Moreover, the anterior cingulate cortex and the anterior insula represented key areas for conflict monitoring, either by receiving input from other areas of the FPAN or by generating input themselves. As it has been reported that the FPAN is influenced by ageing, and seems to be associated with mental illnesses such as schizophrenia and attention-deficit-hyperactivity disorder, it is anticipated that our results will have an impact on future research on distortions of the FPAN.
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In the directory data you will find three subdirectories to access different types of data. All data consists of neuromagnetic signals from 13 different subjects.
In this subdirectiory we provide the averaged source time courses of 14 regions of interest (see paper) for all 13 subjects.
In this subdirectory, the unfiltered dynamics of the ROI source time courses are provided on which Granger causality was applied to investigate the interconnections between the active brain regions, as well as their directionality.
In this subdirectory, the response time for each subject and condition is provided in the file 'Behavioural_data.xlsx'
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Iannaccone R, Hauser TU, Staempfli P, Walitza S, Brandeis D, Brem S. Conflict monitoring and error processing: New insights from simultaneous EEG–fMRI. Neuroimage. 2015;105: 395–407. doi:10.1016/j.neuroimage.2014.10.028
Ptak R. The Frontoparietal Attention Network of the Human Brain. Neurosci. 2012;18: 502–515. doi:10.1177/1073858411409051
Wittfoth M, Buck D, Fahle M, Herrmann M. Comparison of two Simon tasks: Neuronal correlates of conflict resolution based on coherent motion perception. Neuroimage. 2006;32: 921–929. doi:10.1016/j.neuroimage.2006.03.034
Cohen MX, Ridderinkhof KR. EEG Source Reconstruction Reveals Frontal-Parietal Dynamics of Spatial Conflict Processing. Maurits NM, editor. PLoS One. 2013;8: e57293. doi:10.1371/journal.pone.0057293
Pastötter B, Hanslmayr S, T. Bäuml K-H. Conflict processing in the anterior cingulate cortex constrains response priming. Neuroimage. 2010;50: 1599–1605. doi:10.1016/j.neuroimage.2010.01.095
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Simon JR, Small AM. Processing auditory information: Interference from an irrelevant cue. J Appl Psychol. 1969;53: 433–435. doi:10.1037/h0028034
Florin E, Gross J, Pfeifer J, Fink GR, Timmermann L. The effect of filtering on Granger causality based multivariate causality measures. Neuroimage. 2010;50: 577–88. doi:10.1016/j.neuroimage.2009.12.050
Maris E, Oostenveld R. Nonparametric statistical testing of EEG- and MEG-data. J Neurosci Methods. 2007;164: 177–90. doi:10.1016/j.jneumeth.2007.03.024
Harding IH, Yücel M, Harrison BJ, Pantelis C, Breakspear M. Effective connectivity within the frontoparietal control network differentiates cognitive control and working memory. Neuroimage. 2015;106: 144–153. doi:10.1016/j.neuroimage.2014.11.039
Conflict processing networks: a directional analysis of stimulus-response compatibilities using MEG in the data directories by Institute of Neuroscience and Medicine (INM-4), Forschungszentrum Jülich, Jülich, Germany is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License..
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