Fourteen children with attention-deficit hyperactivity disorder (ADHD) and 14 normal control children were compared with respect to stimulus- and response-related processes. Subjects with ADHD took part in two additional sessions under methylphenidate or placebo. In both experiments, performance and electrophysiological measures such as the P2, N2, and P3 components of event-related potential and electromyogram (EMG) activity were measured during an Eriksen flanker task. In both groups of children, reaction times (RTs) to arrow stimuli incongruent with the target were longer than those to neutral stimuli (response interference), which were again slower than RTs to target-alone stimuli (perceptual interference). Children with ADHD made more errors to incongruent stimuli and showed more response interference. For correct responses, no differences between the groups in response interference effects on reaction time, P2, N2, and P3 latency, or EMG onset were found. Methylphenidate had a general enhancing effect on accuracy but did not specifically reduce interference from the flanking stimuli. Methylphenidate had no effects on RT, N2 and P2 latency, P3 amplitude or latency, or EMG activity. The conclusion that methylphenidate did not influence response processes contrasts sharply with findings reported by authors using the Sternberg memory search task.

Asymmetry of waking electroencephalography (EEG) alpha power in frontal regions has been correlated with waking emotional reactivity and the emotional content of dream reports. Little is known regarding alpha asymmetry during sleep. The present study was performed to compare alpha power and alpha power asymmetry in various brain regions across states of sleep and wakefulness. Waking and sleep EEG were recorded in a group of patients undergoing polysomnographic evaluation for possible sleep disorders. Alpha EEG asymmetry in frontal and temporal regions was significantly correlated in waking versus sleep, particularly during rapid eye movement (REM) sleep. These results suggest that patterns of frontal alpha asymmetry are stable across sleep and waking and may be related to emotional reactivity during dreaming. During sleep, alpha power was highest during slow-wave sleep and lowest during REM sleep. Implications of these data for understanding the functional significance of alpha power during waking and sleeping are considered.

Thirty scalp sites were used to investigate the specific topography of the event-related potentials (ERPs) related to face associative priming when masked eyes of familiar faces were completed with either the proper features or incongruent ones. The enhanced negativity of N210 and N350, due to structural incongruity of faces, have a “category specific” inferotemporal localization on the scalp. Additional analyses support the existence of multiple ERP features within the temporal interval typically associated with N400 (N350 and N380), involving occipitotemporal and centroparietal areas. Seven reliable dipole locations have been evidenced using the brain electrical source analysis algorithm. Some of these localizations (fusiform, parahippocampal) are already known to be involved in face recognition, the other ones being related to general cognitive processes related to the task's demand. Because of their specific topography, the observed effects suggest that the face structural congruency process might involve early specialized neocortical areas in parallel with cortical memory circuits in the integration of perceptual and cognitive face processing.

The effects of stimulus intensity, duration, and risetime on the autonomic and behavioral components of orienting, startle, and defense responses were investigated. Six groups of 10 students were presented with 15 white noise stimuli at either 60 or 100 dB, with controlled risetimes of either 5 or 200 ms, and at stimulus durations of 1 or 5 s (1 s only in the case of the 60-dB groups). A dishabituation stimulus consisting of a 1000 Hz tone was also presented. Measures consisted of skin conductance and heart rate, together with ratings of facial expressions and upper torso movement obtained using video recording. Increased intensity resulted in greater amplitudes and frequencies of electrodermal and behavioral responses, and a change from cardiac deceleration to acceleration. Faster risetimes elicited larger electrodermal responses, greater frequencies of eye-blinks, head and body movements, and larger cardiac accelerations. The effects of duration for the 100-dB stimuli were less clear-cut. Overall, the results are discussed in relation to the differentiation of orienting, startle, and defense responses.

Increased frequency of anticipatory saccades during smooth pursuit eye movements is a potential marker of genetic risk for schizophrenia even in the absence of clinical symptomology. The operational definition of anticipatory saccades has often included an amplitude criterion; however, these amplitude criteria have often differed across studies. This study reports on the effect of varying amplitude criteria on the effect size in a comparison of 29 schizophrenic adults and 29 normal subjects during a 16.7°/s constant velocity task. The inclusion of small amplitude anticipatory saccades, with amplitudes of 1–4°, consistently increased effect size (largest effect size = 1.61). The inclusion of large anticipatory saccades, with amplitudes of 4° or greater, had an inconsistent impact on effect size. The separation of anticipatory saccades into leading saccades (anticipatory saccades with amplitude 1–4°) and large anticipatory saccades (amplitude >4°) deserves further exploration.

We investigated emotional disturbances in 36 schizophrenia patients, 48 of their first-degree relatives, and 56 controls to determine if abnormal affective startle modulation could be associated with genetic risk for schizophrenia. Both patients and relatives had a pattern of startle modulation indistinguishable from controls, with potentiated startle amplitude while viewing negative valence slides and attenuation while viewing positive slides. Patients with flat affect did not differ from those without in startle modulation or slide ratings. The patients and their relatives had lower pleasantness ratings of positive slides and the patients had higher pleasantness ratings of the negative slides than controls. The startle paradigm may not be useful for identifying individuals with a genetic liability for schizophrenia. The results suggest that low-level defensive and appetitive behaviors are unaffected in schizophrenia.

Transcranial cortical magnetic stimulation (CMS) is a noninvasive, non-noxious procedure to induce perceptual attenuation when applied concomitant to sensory stimuli. To investigate the perceptual timing of simple stimulus features in the somatosensory modality, we applied right hemisphere CMS at different intervals following a stimulus delivered to the left hand. Different intervals between peripheral stimuli and CMS were defined according to the components of the somatosensory-evoked potentials (SEP), previously obtained in response to the same stimulus. Perceptual attenuation was maximal when CMS coincided with the primary cortical response (parietal N20 potential); conversely, perception of stimulus intensity was not modified when CMS was concomitant with the N200 and P300 potentials. Using small CMS intensities, a “perceptual dip” was observed when CMS arrived in coincidence with the N120 potential, a SEP response thought to be originated in part in the second somatic area. Our results support the view that both N200 and P300 are post-perceptual responses. The results also suggest that the cortical processes active during the N20 and N120 potentials may be essential for the conscious perception of somatosensory stimuli delivered to the hand.

In the current study, we examined lipid and cardiovascular responses to an acute stressor among men with and without a parental history of myocardial infarction. 37 men were selected from a large group who completed medical history questionnaires and interviews. Twenty-two men who denied parental history of heart disease (negative parental history) were compared with 15 men with one or both parents who had suffered a myocardial infarction (positive parental history). Total cholesterol, high- and low-density lipoprotein cholesterol, triglycerides, heart rate, and blood pressure were measured at rest and during a videotaped speech stressor. Positive parental history men had significantly higher low-density lipoprotein cholesterol levels and blood pressure at baseline, significantly lower high-density lipoprotein cholesterol levels at baseline, and significantly larger total cholesterol and low-density lipoprotein cholesterol reactivity, relative to negative parental history men. Because parental history is a risk factor for subsequent cardiovascular morbidity and mortality, these data suggest that lipid reactivity to stress may be biologically important.

Attentional modulations of event-related brain potentials (ERPs) were measured when subjects were cued to attend to a visual quadrant or to a ring-shaped region of visual space to detect infrequently presented targets within the attended region. Spatial attention directed to quadrants was reflected in modulations of sensory-evoked P1 and N1 components at lateral posterior sites and enhanced negativities (Nds) at midline electrodes that started around 150 ms poststimulus. When attention was directed to ring-shaped regions, no modulations of P1 and N1 amplitudes were found, and Nd effects observed at midline electrodes were delayed by about 50 ms. These findings indicate that behavioral effects observed both when attention is directed to contiguous regions and to general areas of visual space may be caused by different underlying processes. Intraperceptual “sensory gating” mechanisms operating in a way suggested by the notion of an attentional “zoom-lens” may be responsible for the selection of single regions, quadrants, or hemifields. When relevant regions are more complex, spatial selectivity will affect primarily postperceptual processes.

Research has indicated that performance on heartbeat counting tasks may be influenced by beliefs about heart rate. Sixty male subjects were administered the Schandry heartbeat counting task after viewing fast, slow, or no heart rate feedback. Subjects were also administered the Whitehead signal-detection type task. Results indicated that subjects who received fast or no heartbeat feedback performed better on the Schandry task than subjects who received slow feedback. Feedback presentation did not affect performance on the Whitehead task. These results suggest that the Schandry task is influenced by external variables (expectations, beliefs) beyond pure awareness of “discrete” visceral sensations and, thus, may not be as powerful a method for determining awareness of individual heartbeats as some other paradigms.

Subcomponents of the N200 component of the event-related brain potential believed to be differentially sensitive to involuntary and voluntary cognitive processes were examined. Nonpatients (N = 131) identified initially by the Chapman and Depue research scales and classified later on the basis of diagnostic symptom clusters and family psychiatric history provided converging evidence for an intact mismatch negativity subcomponent. In contrast, the N2b subcomponent distinguished several groups of subjects. Results suggested abnormal voluntary cognitive processing, perhaps reflecting compensatory efforts in subjects at risk for or manifesting psychopathology, particularly those showing negative symptoms.

Choice reaction time (RT) is shorter when the stimulus corresponds spatially to the response than when the stimulus does not, even when the stimulus location is irrelevant to the task. We used electromyographic measures to document that this effect is the result of a response conflict. The activity of the prime movers of two alternative responses was recorded during the performance of a visual RT task in which the irrelevant spatial correspondence between the stimuli and the responses was varied. Only the premotor component of RT was affected by the stimulus–response correspondence. Correct trials were distinguished according to whether or not the activation of the prime mover involved in the required response was preceded by an activation of the prime mover involved in the alternative response. Double muscular activation trials were more numerous for noncorresponding than for corresponding stimulus–response associations. Furthermore, these trials yielded longer RTs than the single muscular activation trials.

In a recent paper, Pritchard, Krieble, and Duke (Psychophysiology, 33, 362–368, 1996) studied the validity of spatial embedding of electroencephalographic (EEG) data and rejected this method in favor of time-delay embedding. The present paper describes the nonlinear characterization of brain dynamics using either spatial or time-delay embedding. We discuss the arguments published in Pritchard et al. (1996) and demonstrate that the spatial embedding cannot be rejected on this basis. We also point out the limitations of both spatial and time-delay embeddings related to the spatial extension and the high-dimensional dynamics of brain activity.

Careful consideration of the issues raised by Pezard and colleagues (in this issue of Psychophysiology) allows for the conclusion that spatial embedding may be valid as a method of dynamical reconstruction. However, two problems with the technique cannot be ignored. First, spatial embedding of EEG invariably involves linear cross-correlation among channels, which distorts the dynamical reconstruction due to compression toward the main state-space diagonal. Further, before spatially embedding across a set of channels, one must first check for at least “similar” dynamics among them, using, for example, a measure such as estimated mutual dimension. Measuring a “whole cortex” state via spatial embedding may also be possible in principle, except for the nontrivial obstacle of separating local dynamics that are heterogeneous across the cortex from activity reflecting the “unified field” of the cortex as a whole.