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Summary A sound lasting for several seconds is known to elicit a basline shift in electrical and magnetic records. We have studied the dependence of the magnetic field distribution of this "per-stimulatory" sustained field (SF) on tone frequency. Tone bursts of 2 sec duration and 60 dB nHL intensity were presented to 11 subjects at varying interstimulus intervals between 5 and 7 sec. The carrier frequencies of 250, 1000 and 4000 Hz varied randomly from trial to trial. The field distributions obtained are consistent with the view that the auditory evoked sustained field activity originates in the supratemporal cortex. Differences in the locations of equivalent current dipoles of the SF from those of the MlOO wave of the slow auditory evoked field are consistent across subjects. The SF source locations corresponding to stimulus frequencies over an extended frequency range are arranged in a tonotopic manner and support the idea that the sources of the MlOO and the SF are current dipole sheets located on the superior surface of the primary auditory cortex.

A widespread depolarization in the dendritic trees of cortical pyramidal neurons generates surface-negative potentials. In turn, such potentials may indicate facilitatory processes while positive-going waves may result from a lowering in cortical excitability. Accordingly, we may expect the processing of “probe” stimuli presented during surface-positive waves, i.e., during phases of lesser excitability, to be inhibited and probes presented during surface-negative waves to be facilitated. This hypothesis was tested by presenting acoustic probe stimuli at various points in time during a forewarned reaction time task. The warming stimulus (WS) elicited a late positive complex followed by a negative slow potential shift (CNV). In 75% of the total of 120 trials a probe could be presented 1.5 sec prior to the WS interval, 0.5, 1, 1.5 or 2 sec after the onset of the 3 sec visual WS, and 3 sec following the imperative signal (WS offset, requiring a fast button press response), while 25% of the trials were without any probe. Only one probe occurred during a trial. The EEG was recorded along the midsagittal line; responses to the probes were evaluated by reaction time (RT) and probe-evoked potentials. RT to probes presented late in the anticipatory interval were speeded up and probe-evoked potentials were enhanced during this interval, in parallel to the development of the slow potential and the CNV in particular. Results suggest that probe stimuli presented during the development of the CNV were processed more intensely, thereby supporting the hypothesis that slow cortical potentials indicate the timing of excitability in cortical neuronal networks. Such a tuning mechanism may serve as a basis for attentional regulation.

The effects of the benzodiazepine clonazepam (a drug used as anticonvulsant) on event-related brain potentials ewere investigated in healthy human subjects. Thirty-six male student volunteers (mean age 30 years) received clonazepam or a placebo in a double-blind setting. VEPs (visual evoked potentials) were obtained from the standard checkerboard reversal procedure; AEPs (auditory evoked potentials) and slow cortical potentials (CNV) were measured during a 2-stimulus reaction time paradigm, in which the quality of the acoustic S1 signalled whether the acoustic S2 would follow after 2 sec or afer 6 sec. Each S2 requested a speeded button press. Compared to placebo, clonazepam significantly reduced P100 amplitude of the VEP and the amplitudes of the AEP components N1 and P3. On the other hand, clonazepam boosted the development of a distinct N2 which was not apparent in placebo subjects. The CNV was significantly reduced and reaction time increased under clonazepam compared to placebo. Specific versus non-specific damping effects of the benzodiazepine are discussed, comparing the present result with the pattern of ERP effects of the anticonvulsant carbamazepine that had been obtained using the same experimental paradigms.

Meaningful words and matched pseudowords, such as moon vs. noom, are of equal perceptual complexity, but invoke different cognitive processes. To investigate high-frequency cortical responses to these stimuli, biomagnetic signals were recorded simultaneously over both hemispheres of right-handed individuals listening to words and pseudowords. Consistent with earlier EEG studies, evoked spectral responses recorded from the left hemisphere revealed depression of spectral power in the low gamma band (around 30 Hz) after pseudowords but not after words. Similar differences between stimulus categories were present in the beta range. These results indicate that distinct patterns of high-frequency cortical responses correspond to the different cognitive processes invoked by words and pseudowords. It is hypothesized that differential high-frequency cortical responses signal the activation or activation failure of distributed Hebbian cell assemblies representing words and other elements of cognitive processing.

Cerebral responses in anticipation of painful stimulation and while coping with it were investigated in a "fakir" and 12 male volunteers. Experiment 1 consisted of 3 periods of 40 trials each. During period 1, subjects heart one of two acoustic warning stimuli of 6 sec duration signalling that either an aversive noise or a neutral tone would be presented at S1 offset. During period 2, subjects were asked to use any technique for coping with pain that they had ever found to be successful. During period 3, the neutral S2 was presented simultaneously with a weak electric shock and the aversive noise was presented simultaneously with a strong, painful shock, again under pain copying instructions. EEG activity within the theta band increased in anticipation of aversive events. Theta peak was most prominent in the fakir's EEG. A negative slow potential shift during the S1-82 interval was generally more pronounced in anticipation of the aversive events that the neutral ones, even though no overt motor response was required. Negativity tended to increase across the three periods, opposite to the usually observed diminution. In Experiment 2, all subjects self-administered 21 strong shock-noise presentations. The fakir again showed more theta power and more pronounced EEG negativity after stimulus delivery compared with control subjects. Contrary to the controls, self-administration of shocks evoked a larger skin conductance response in the fakir than warned external application.

An experiment was performed to investigate the self-regulation of slow cortical potentials (SCP) found in a previous study (Elbert et al. 1979). Seventeen subjects received continuous visual feedback of their actual cortical shift perceptible as a rocket moving across a TV-screen during intervals of 6 sec; subjects had to direct the rocket into one of two goals representing more or less cortical negativity, depending on the pitch of two signal tones. Within two identical experimental sessions feedback trials alternated with test trials without feedback. Highly significant differences of SCP between the two required polarities were demonstrated. The most pronounced differences were observed during test trials without feedback of the second session in which a positive shift below baseline level occurred when positivity (or less negativity) was required.

The present paper describes the propagation of ocular potentials across the scalp on a biophysical basis. It is concluded that 3 EOG derivations (two for EEG records along the midline) are generally necessary to account for ocular disturbances in the EEG. The inadequacy of many methods suggested for EOG artifact control may be due to the false assumption that just one EOG derivation provides enough information to remove ocular potentials from any EEG recording along the mid(-sagittal) line. A comparison of compensation with one or with two EOG derivations is described for a data set of slow brain potentials. A frequency dependence of the ocular influence cannot be neglected, if fast and slow EOG activities have to be removed. The present considerations should allow a more theoretically based decision of the EOG correction method necessary for a certain data set.

A single trial analysis of slow cortical potentials treating the EEG as a time series was developed. The method was applied to data resulting from an experiment on self-regulation of slow cortical potentials (SCP). Parametric models of the EEG were developed on the basis of autoregressive filter models and a two-component model of SCP (during 6 sec intervals), taking into account ocular influences as a further parameter. Results from different models were compared with each other and with results of averaging SCP data. For the present data time series analysis and traditional analysis provided qualitatively equal results, but fewer trials were necessary for analysis in the single trial approach and more detailed structures of the data became evident. If the EEG was filtered above 5 Hz it could be described by an autoregressive filter model of low order. Ocular influences were estimated as too small in a non-filtered EEG compared to the filtered EEG.