Abstract

Cortical potentials were recorded from implanted electrodes during a difficult working memory task requiring rapid storage, modification and retrieval of multiple memoranda. Synchronous event-related potentials were generated in distributed occipital, parietal, Rolandic and prefrontal sites beginning ∼130 ms after stimulus onset and continuing for >500 ms. Coherent phase-locked, event-related oscillations supported interaction between these dorsal stream structures throughout the task period. The Rolandic structures generated early as well as sustained potentials to sensory stimuli in the absence of movement. Activation peaks and phase lags between synaptic populations suggested that perceptual processing occurred exclusively in the visual association cortex from ∼90 to 130 ms, with its results projected to fronto-parietal areas for interpretation from ∼130 to 280 ms. The direction of interaction then appeared to reverse from ∼300 to 400 ms, consistent with mental arithmetic being performed by fronto-parietal areas operating upon a visual scratch pad in the dorsolateral occipital cortex. A second reversal, from ∼420 to 600 ms, may have represented an updating of memoranda stored in fronto-parietal sites. Lateralized perisylvian oscillations suggested an articulatory loop. Anterior cingulate activity was evoked by feedback signals indicating errors. These results indicate how a fronto-centro-parietal ‘central executive’ might interact with an occipital visual scratch pad, perisylvian articulatory loop and limbic monitor to implement the sequential stages of a complex mental operation.

Introduction

Working memory maintains information for use in on-line cognition. As conceptualized by Baddeley, working memory is composed of a central executive controlling ‘slave systems’, primarily a ‘visuospatial scratch pad’ and an ‘articulatory loop’ (Baddeley, 1986). Working memory thus combines a mental workspace with short-term buffers and executive processes for interpreting incoming stimuli, updating actively stored items accordingly, and maintaining the intermediate results of processing for further calculations. Working memory has become a key concept in many models of higher cognitive activities such as reading (Just et al., 1996). The amount of resources in working memory and the efficiency of their dynamic allocation are seen as the main factors underlying limitations in fundamental intellectual abilities (Kyllonen and Christal, 1990).

In some working memory tasks, a single stimulus is presented, then retained as presented for ∼2–30 s and finally retrieved. Such tasks probe what has been termed primary memory (James, 1890) and are amenable to neurophysiological analysis because the input, retention and retrieval stages are separated temporally. In contrast, other working memory tasks require a rapid interaction between perception, interpretation and memory. Previous studies have used positron emission tomography (PET) or functional magnetic resonance imaging (fMRI) for measuring haemodynamic or metabolic activation during working memory. Both varieties of working memory task activate an extended network of the prefrontal, parietal and medial frontal cortices (Swartz et al., 1995; Fiez et al., 1996; Smith et al., 1998; Ungerleider et al., 1998).

Haemodynamic and neuropsychological studies suggest that it may be possible to distinguish the contributions that these different areas make to working memory. Consistent with a long tradition in neuropsychology, the prefrontal cortex has been associated with executive function (Baddeley, 1986). In some haemodynamic studies, the more ventral prefrontal areas have been associated with the simple retention of material in primary memory, whereas the more dorsolateral areas have been engaged when the task requires a higher level of executive control (Petrides et al., 1993; D'Esposito et al., 1995; Cohen et al., 1997; Owen, 1997; Smith et al., 1998). Other studies have found the location of prefrontal activation to depend upon the nature of the material to be retained, with verbal/non-verbal material mapping to the dominant/non-dominant hemisphere and spatial/ non-spatial material mapping to the dorsal/ventral areas (Smith et al., 1998; Ungerleider et al., 1998). Similarly, lesion studies have suggested that the parietal cortex (in particular near the intraparietal sulcus) is specialized in spatial analysis (Critchley, 1953). Conversely, the left perisylvian activation is associated with the maintenance of information in the articulatory loop according to both neuropsychological (Shallice and Vallar, 1990) and haemodynamic evidence (Fiez et al., 1996). Finally, anterior cingulate activation has been associated with error monitoring and stimulus response mapping (Bush et al., 2000).

These studies support hypotheses associating different cortical areas with different working memory components. However, the task/area double dissociations predicted by these hypotheses are often difficult to obtain. In particular, parietal and anterior cingulate activations in working memory tasks tend to be correlated with prefrontal activation across task conditions (Carpenter et al., 2000; Diwadkar et al., 2000) and a strict correlation of working memory deficits with prefrontal lesions has not been found (Frisk and Milner, 1990). Co-activation of a parieto-fronto-cingulate network has also been found in other tasks, in particular those involving attention (Corbetta, 1998) and task difficulty/self-monitoring/response choice (Cohen et al., 2000). Similarly, neuroanatomical and neuropsychological evidence supports an integrated parieto-fronto-cingulate circuit in executive functions (Goldman-Rakic, 1988; Mesulam, 1990). Finally, efforts to isolate cortical areas that are exclusively activated by the necessity of controlled allocation of attentional resources in dual task situations have yielded inconsistent results, suggesting that high-level executive functions may arise through the interaction of multiple structures (Adcock et al., 2000).

One interpretation of these data is that, although the parietal and prefrontal cortices make distinct contributions to complex processing (as revealed by lesions), they are so interconnected that their activation patterns are nearly indistinguishable. Alternatively, it is possible that the different structures not only have distinct functions but that they are activated sequentially and this cannot be seen with haemodynamic measures because of their poor temporal resolution (>∼1 s) (Buxton et al., 1998; Dale and Halgren, 2001). That is, although these areas are coactivated on a time-scale of ∼1 s and belong to the same general system, it is conceivable that their activation is modular and sequential rather than continuously interactive and overlapping.

The spatiotemporal dynamics of cortical activation during working memory also have implications for whether the prefrontal cortex acts in working memory as a repository of primary memory, as opposed to as the central executive. As primary memory, specific and sustained firing of prefrontal neurons would encode significant memoranda as well as the cognitive context. This sustained firing would function not only as a memory store but also as a source of task-specific instructions and temporal markers for the posterior association cortex, thus freeing it from immediate sensory input (Goldman-Rakic, 1988; Fuster, 1989; Halgren, 1994). Alternatively, as central executive, the prefrontal cortex would provide goal-directed sequencing and control of the posterior association cortex. Initially, this control directs attention to a sensory channel by activating the associated cortical area (Desimone, 1996; Hillyard and Anllo-Vento, 1998; Mangun et al., 1998; Knight et al., 1999). Subsequent executive control can be conceptualized as an extension of this process, with the prefrontal cortex successively activating cortical areas concerned with perceptual processing, interpretation of the stimulus with respect to task instructions, consequent mental operations on active memoranda, memory updating and response selection. These central executive functions would imply phasic activation of prefrontal neurons corresponding to the successive processing stages.

A related question is whether primary memory is held in the prefrontal cortex or the posterior sensory association cortex or both. If it is only in the prefrontal cortex, then sensory association areas may complete their work soon after stimulus presentation, pass the results to anterior areas and then no longer be active. Conversely, the model mentioned above (Baddeley, 1986) suggests that sensory association areas are involved in later stages simultaneously with higher cortical areas, in particular in the prefrontal cortex.

In summary, an adequate neural model of working memory should specify not only which structures are involved, but also the dynamics of their interaction. The most extensive source of data regarding these dynamics is unit-recording studies in macaques during working memory (Goldman-Rakic, 1988). Sustained stimulus-specific firing by prefrontal neurons supports the hypothesized prefrontal contribution to primary memory. However, phasic firing patterns are also observed in prefrontal neurons and, conversely, the same categories of task-related firing are observed in temporal and parietal sites, with the time-course of activation in these areas entirely overlapping with prefrontal activation (Fuster, 1989; Chafee and Goldman-Rakic, 1998). Furthermore, the parietal and prefrontal firing patterns are modified but fundamentally maintained during cooling of either location, suggesting that they arise out of the coordinated activity of an extended network (Fuster et al., 1985; Chafee and Goldman-Rakic, 2000). The lack of stronger effects is interpreted as being due to the high degree of redundancy in connections in the generating circuit (Goldman-Rakic, 1988). However, the similarity of activation in different areas that seems to reflect their seamless integration leaves no leverage for explicating their distinct roles (Chafee and Goldman-Rakic, 2000). Furthermore, it is uncertain how to generalize these results to humans in more complicated working memory tasks that engage the central executive heavily.

Direct electrophysiological recordings in humans during working memory would thus be useful in understanding the temporal dynamics of engagement by different cortical areas. Such recordings with scalp electrodes have also been interpreted as indicating continuing interactions between the anterior and posterior cortex (Gevins et al., 1996). However, the cortical generators of these signals cannot be inferred unambiguously (Hamalainen et al., 1993; Dale and Halgren, 2001). Intracranial electroencephalography (iEEG) recordings have high temporal resolution and under some circumstances can also localize generators with high spatial resolution (Halgren et al., 1980). Such recordings can only be obtained from electrodes implanted for clinical purposes and, thus, are limited by possible contamination with pathological activity, as well as clinical limitations in spatial sampling. Nonetheless, they offer a view of the spatiotemporal activation patterns that underlie cognitive events, which is complementary to non-invasive measures.

In the current study, we report the results of intracranial recordings during Mental Counters, a working memory task that requires the rapid perception and evaluation of six successive stimuli interleaved with the maintenance and updating of active memoranda (Larson and Saccuzzo, 1989). The memoranda were digits or figures in different variants that were intended to probe different material-specific ‘scratch pads’. Following the input stimuli, a probe stimulus was presented and then a feedback tone following the response.

The results are most consistent with a sequential but not modular model of cortical function in working memory. Although early processing was briefly confined to the visual association cortex, activation soon spread to multiple occipital, parietal and frontal sites, which all remained active for the entire epoch. In particular, the co-activation of visual association with the fronto-parietal cortices suggests that it contributes to working memory beyond perceptual analysis. The results support the presence of at least four processing stages in working memory, with each lasting ∼50–200 ms. Phase-locked oscillations from ∼4 to 12 Hz were prominent in multiple structures including the prefrontal cortex, as would be expected if it contributes to the central executive. Single-trial spectral analysis of the dominant oscillations suggested organized interactions between the areas, with rapidly shifting directions of information flow. Event-related oscillations ranged from 4 to 50 Hz. They were commonly embedded in slower oscillations synchronized with the individual stimuli (∼1 Hz), which in turn were embedded in sustained activation from the first stimulus to the probe (<0.1 Hz). The latter supports a primary memory contribution of the prefrontal cortex to working memory. Limbic areas, in particular the anterior cingulate gyrus, were preferentially activated by the probe and feedback stimuli. Overall, the results reveal multiple embedded oscillations that may reflect the temporal organization of processing and memory functions across multiple cortical areas during this difficult task.

Materials and Methods

Patients

Seventeen patients (10 females and seven males) suffering from intractable partial epilepsy consented to participate in this study while undergoing iEEG for possible neurosurgical treatment. All subjects except one were right-handed and that subject was left dominant for language according to the Wada test. Their mean age was 26.2 ± 7.7 years.

The subjects performed different variants of the Mental Counters paradigm of Larson, which were modified to be appropriate for neurophysiological recordings in patients (Larson and Saccuzzo, 1989). These tests all required the maintenance of different memoranda and their updating in response to rapidly presented stimuli. In the standard numeric paradigm with two memoranda presented in the visual modality (N2V), the location of the stimuli indicated which memorandum was to be operated on and which operation was to be performed on it (Fig. 1). Based on preliminary testing with a control group, NV2 was chosen as the basic task variant to be given to all patients. Of the 17 subjects, 16 performed the N2V variant. Some subjects also performed variants of the Mental Counters paradigm that differed from N2V in material (using figures or letters instead of numbers, i.e. F2V or L2V), modality (auditory rather than visual, i.e. N2A) or memory load (three rather than two memoranda, i.e. N3V). Note that, in all of the visual variants, identical stimuli were used and the tasks were different only in the nature of the memoranda and the operations to be performed upon them. Of the 17 subjects, 10 performed the F2V variant, four the L2V variant, three the N3V variant and only one the N2A variant. Each trial consisted of six stimuli, 36 trials were presented per block and one to four blocks of a variant were obtained in a particular subject. In addition to electrophysiological recordings, reaction times and response accuracy were obtained.

The study was described to the subject in the subject's hospital room, usually on the day prior to recordings and informed consent was requested. The subjects then participated in a training session of 45 min during which each variant was initially presented with inter-stimuls intervals (ISIs) of 2500 ms. This was gradually decreased to 1240 ms and finally 960 (nine subjects) or 840 ms (eight subjects) if the patient was capable. Approximately half of the patients receiving training were unable to perform the task at an acceptable speed, presumably due to psychomotor slowing induced by anticonvulsant medications. Physiological recordings were only obtained from the remaining 17 subjects.

Numbers–Two Memoranda–Visual (N2V)

At the beginning of each trial the initial values of the memoranda (three zeros) were presented on the left, right and middle of a 16 in colour monitor. When the subject pressed a key, three zeros were replaced in the same positions by three points. Then at ISIs of 840 ms (240 ms stimulus exposure) a short line appeared. If the line was horizontal (42%) or vertical (42%) then the subject made a subtraction or addition to either the left or right memorandum, according to the location of the target. If the line was above a dot then the operation was addition of one and if the line was below a dot then the operation was subtraction. The new result was maintained in memory to be used as a basis for the next line. Diagonal lines (16%) indicated that no operation was to be performed (i.e. ‘catch’ trials). Six lines were presented in each trial. The location of the lines and their orientation varied randomly on successive presentations with the exception that the correct value of any given memorandum was maintained between –3 and +3. At the end of these six presentations a proposed solution consisting of three numbers was provided on the screen, one at each of the original dot locations. Fifty percent of the proposed solutions matched the correct result. The subject had to press the left key in <3 s if the proposed solution was correct and the right key if it was not. A feedback tone indicated whether the subject's answer was correct (high tone) or not (low tone). Throughout the entire trial the subject maintained fixation on the centre of the monitor, which was occupied by either a dot or a number. The response and feedback procedures as well as all time-intervals and stimulus-type proportions were identical across all variants.

Numbers–Three Memoranda–Visual (N3V)

N3V was identical to N2V, except that the lines could appear above or below the middle point on the monitor, i.e. three rather than two memoranda needed to be maintained in memory and incremented or decremented accordingly.

Numbers–Two Memoranda–Auditory (N2A)

N2A used sounds as the stimuli. As in N2V each trial started with the presentation of three zeros on the left, right and centre of the monitor. The dots then remained on the screen until they were replaced with the response probe. Throughout this period the subject maintained fixation on the centre dot. Adding one to the memorandum was signalled by pure high-pitched sounds, subtraction by low-pitched sounds and catch trials by complex sounds. In order to indicate that the operation was to be carried out on the right-side memorandum, the sound was presented in the right ear and vice versa. After six sounds a solution was proposed on the screen.

Letters–Two Memoranda–Visual (L2V)

L2V used letters as the memoranda. Each trial began with three Ls on the left and right and in the centre of the monitor. These were replaced by dots and then short lines started appearing above or below the left or right dot, exactly as in N2V. Horizontal or vertical lines above dots signalled going ‘up’ a letter (or backwards) in the alphabet (e.g. L to K) and targets below dots signalled going ‘down’ a letter (e.g. L to M). Again, diagonal lines signalled no operation. After six lines were processed a response probe consisting of three letters was presented.

Stereoencephalographic Recordings and Stimulation

Stereoencephalographic (SEEG) recordings were obtained from a total of five to eight multicontact probes surgically inserted into the depths of one or both cerebral hemispheres of each patient (Fig. 2). The anatomical location of these probes was decided entirely on clinical grounds for localizing the origins of the patients' epileptic seizures (Chauvel et al., 1996a). Typically, the probes remained implanted for 4–7 days in order to obtain recordings during seizure activity. The recordings in the present study were obtained during seizure-free periods. Each probe contained between five and 15 stainless steel contacts, thereby allowing for recordings from different medial to lateral sites aligned perpendicular to the sagittal plane (Fig. 2). The contacts were 2.0 mm in length and were separated by 1.5 mm. Recordings were obtained across all 17 subjects from 667 left hemisphere and 701 right hemisphere sites. The contacts were localized using human stereotaxic statistical data (Talairach et al., 1967; Talairach and Tournoux, 1988) and confirmed with stereoscopic stereotaxic angiography (Szikla et al., 1977) and, in most cases, stereotaxic MRI (Musolino et al., 1990). The probes are lettered (primed in the left hemisphere). The contacts are numbered according to their distance from the midline in millimetres. The contact locations are also indicated in Talairach's coordinates (x = distance to the right of the midline, y = distance forward from the anterior commissure or AC and z = height above the anterior commissure–posterior commissure or AC–PC line) (Talairach and Tournoux, 1988). The actual coordinates are listed first, then normalized in italics. Since the y and z coordinates are constant for all contacts of a given probe, they are omitted where they are clear from the context.

In many cases, the contacts were stimulated electrically in order to delineate the origin and spread of seizure discharges better (Chauvel et al., 1996a). Unless otherwise noted, these stimulations were bipolar between adjacent electrode contacts, with pulses of 1 ms delivered in a train of 5 s at 50 pulses/s at stimulus intensities below that necessary for evoking a local after-discharge (as monitored by simultaneous SEEG recordings). Those stimulations with effects that provided confirmation of functional localizations are presented below.

The contacts were located in the following regions (the counts include contacts located in the underlying white matter): the occipital cortex (n = 62), precuneus and superior parietal lobule (n = 15), posterior cingulate gyrus (n = 60), supramarginal gyrus (n = 128), lingual and fusiform gyri at the occipitotemporal junction (n = 30), middle temporal gyrus at the occipitotemporal junction (n = 48), posterior hippocampal formation (n = 70), posterior middle temporal gyrus (n = 105), anterior hippocampal formation (n = 80), middle level of the middle temporal gyrus (n = 117), amygdala region (n = 75), anterior level of the middle temporal gyrus (n = 107), posterior superior temporal gyrus (n = 80), anterior superior temporal gyrus (n = 18), ventromedial prefrontal cortex (n = 71), ventrolateral prefrontal cortex (n = 157), dorsomedial prefrontal cortex (n = 15), ventrolateral prefrontal cortex (n = 24), paracentral gyrus (n = 19) and Rolandic cortex (n = 87) (including the precentral and postcentral gyri and sulci). Scalp recordings were usually obtained at Cz or Pz. The specifics of localization are presented in the context of descriptions of individual responses.

Recordings were digitized on-line with an accuracy of 12 bits. In the initial eight subjects, recordings were made as separate epochs during the six input (I1–I6), probe and feedback stimuli at 6 ms per sample with a bandpass of 0.1–35 Hz. The epochs began 40 ms before the stimulus and ended 794 or 914 ms after the stimulus (for the 840 or 960 ms stimulus-to-stimulus onset intervals, ISIs, respectively) for the I1–I6 and probe stimuli. The epochs began 190 ms before the stimulus and ended 644 or 764 ms after the stimulus for the feedback stimuli. Data were acquired continuously in the last 10 subjects during the entire task at 200 Hz and a bandpass of 0.5–50 Hz. This bandpass may have reduced sustained potentials related to primary memory. Eye movement artefacts (>75 μV) were monitored with an electrode placed at the outer canthus of the right eye. Unipolar recordings to a relatively inactive reference (the nose) were employed in order to understand the field distributions in terms of both gradients in amplitude as well as absolute levels. The potentials recorded at the nose relative to a distant (i.e. non-cephalic) reference were negligible in amplitude compared to the amplitude of intracranial potentials and, thus, it can be considered an inactive reference in the current study.

Analysis

The recordings were screened for artefacts (e.g. epileptiform activity and eye or body movements) and then averaged within each task variant in order to yield event-related potentials (ERPs) of input stimuli indicating addition, subtraction or no operation (‘catch’), of true and false probes, and of correct versus incorrect responses. In addition, ERPs were made of the entire trial in order to identify longer duration processes. These whole-trial ERPs in the initial eight subjects were made by concatenating the ERPs to all conditions of the I1–I6, probe and feedback epochs. Consequently, the ERPs began 40 ms before the I1 epoch and ended 644 or 764 ms after the feedback epoch, with small gaps between the I6 and probe epochs and between the probe and feedback epochs. Data were acquired continuously in the last 10 subjects, thereby permitting a continuous epoch from before the I1 epoch until after the feedback epoch.

Previous studies have suggested that most task-related EEG activity is not phase locked to the evoking stimulus and thus does not contribute to the ERP (Klopp et al., 1999; Tallon-Baudry and Bertrand, 1999). Furthermore, averaging obscures the temporal relations between EEGs in different structures. In order to obtain a more comprehensive estimate of task-related responses, the individual trial spectral power, phase locking and phase lag were calculated using a wavelet function for different frequencies and latencies with respect to the stimulus. The resulting time–frequency plots were averaged across trials and normalized with respect to the pre-stimulus baseline. For these measures, the single trial signal si(t) for each channel i was convoluted with complex Morlet's wavelets w(t,f0):

$\mathit{TF}_{\mathit{i}}(\mathit{t},\mathit{f}_{0})\ {=}\ \mathit{w}(\mathit{t},\mathit{f}_{0})\ {\times}\ \mathit{s}_{\mathit{i}}(\mathit{t})$
The time–frequency representation TFi(t,f0) has both amplitude [Ai(t,f0)] and phase [ϕi(t,f0)] information. The estimated spectral amplitude is the average of Ai(t,f0) across all trials. The phase-locking factor is defined (Lachaux et al., 1999) as
$PLF_{\mathit{ij}}(\mathit{t},\mathit{f}_{0})\ {=}\ \mathit{E}(exp(\mathit{j}({\phi}_{\mathit{i}}(\mathit{t},\mathit{f}_{0})\ {-}\ {\phi}j(\mathit{t},\mathit{f}_{0}))))$
The phase lag factor is defined as
$PLG_{\mathit{ij}}(\mathit{t},\mathit{f}_{0})\ {=}\ \mathit{E}(angle(\mathit{TF}_{\mathit{j}}(\mathit{t},\mathit{f}_{0})\ {\times}\ \mathit{Tf}_{\mathit{i}}(\mathit{t},\mathit{f}_{0}){\ast}))$
Each Morlet's wavelet (Kronland-Martinet et al., 1987) used here had a Gaussian shape both in the time domain (SD σt) and in the frequency domain (SD σf) around its central frequency f0:
$\mathit{w}(\mathit{t},\mathit{f}_{0})\ {=}\ \mathit{A}exp(\frac{{-}\mathit{t}^{2}}{2{\sigma}_{\mathit{t}}^{2}})exp(2\mathit{i}{\pi}\mathit{f}_{0}\mathit{t})$
with σf = 1/2πσt. Wavelets are normalized so that their total energy is unity, the normalization factor A being equal to (σtπ0.5)−0.5. Relatively constant temporal and spatial resolution across target frequencies were obtained by adjusting the wavelet widths (f0f ratio) according to the target frequency. In the initial eight subjects, the wavelet widths increased linearly from 1.5 to 10 as the frequency increased from 4 to 40 Hz, resulting in a σt value of 60–40 ms and a σf value of 2.7–4 Hz. In the last 10 subjects, the wavelet widths increased from 2 to 13 as the frequency went from 4 to 50 Hz, resulting in a σt value of 79–41 ms and a σf value of 2.0–3.8 Hz. Tests with simulated data confirmed that the methods used here can show clear phase-locking and lag patterns, even at 4 Hz. The findings were confirmed with standard spectral power and coherence measures on successive overlapping windows as described previously (Klopp et al., 1999, 2000).

Like extracranial EEG and magnetoencephalography (MEG), SEEG has high temporal resolution (limited by the sampling interval) but, unlike them, SEEG also has fine anatomical resolution (limited by the spacing between recording sites). Although recordings are only obtained from epileptic patients, recording locations and epochs may be selected where the EEG appears to be normal. Indeed, when it is possible to compare the results from SEEG with those from non-invasive measures in normal subjects, very similar results are obtained. The main limitation of SEEG is incomplete sampling: in order to sample the entire brain at a spacing of 3.5 mm over 10 000 contacts would be needed, but only ∼100 contacts are sampled in each patient. Furthermore, in the tissue that is actively generating the EEG response the amplitude and polarity change rapidly from contact to contact. Thus, it is very difficult to average responses across subjects, even if they are nominally recorded from the same region.

These considerations lead to a data analysis strategy where every recording is examined for rapid changes in amplitude and/or polarity over short distances. Electrode contacts with proof of locally generated ERP components are then further intensively examined for the cognitive correlates of those components (by comparison across other tasks), for the precise location of the contact (anatomically by comparison with MRI and stereotactic arteriography and functionally by comparison with the effects of local electrical stimulation) and for the presence of activation in the spectral domain. When multiple ERP generators in different sites are simultaneously recorded, then evidence for the presence and direction of communication between these sites is sought using phase-locking and phase lag measures. Initial analysis thus treats the data as a series of single-case studies, thereby proving local generation of particular ERP components in particular locations in particular people. The consistency of the data is evaluated by identifying replications across subjects. The certain localization and high spatiotemporal resolution of SEEG can then be used to help in interpreting particular activations identified by fMRI, PET, MEG and/or EEG studies.

Results

Behaviour

Behavioural performance for the two most common task variants is shown in Table 1. On average, the subjects responded correctly in 69% of the trials with a reaction time of 1064 ms to the probe. Performance was slightly better (t-test, P < 0.05) on the version with numerical memoranda (N2V) than that with figural memoranda (F2V), but the reaction times did not differ.

Visual Association Cortices

Multiple inverting evoked potentials were recorded in the dorsal visual pathway, with peaks as early as ∼100 ms and continuing until ∼700 ms, i.e. virtually the end of the recording epoch. Local potential inversions and gradients demonstrated that these potentials were locally generated. The precise anatomical location of the most responsive cortical recording sites indicated that they were in the visual association cortex of the dorsal stream, an inference confirmed in some cases by the effects of local electrical stimulation.

Local electrical stimulation of probe D in patient 2 evoked illusory head movements. The location of probe D (visualized directly on his MRI, Fig. 5) corresponded to that of human visual motion area MT+. Earlier studies have found specific responses in this area to coherent as compared to incoherent movement in humans (Watson et al., 1993; Tootell et al., 1995; Ulbert et al., 2001) and macaques (Lappe and Duffy, 1999; Andersen et al., 2000), leading to theories that assign a role to area MT+ (and in particular to MSTd) in visual flow phenomena, inferring the direction and speed of head motion from coherent visual motion. The current finding that stimulation in this area resulted in a sensation of head motion is consistent with these theories. This contrasts with the experience of moving visual stimuli evoked by stimulation of another visual motion area in the medial parieto-occipital sulcus, which appears to correspond to SPO or V7 (Richer et al., 1991). Illusory head movements were also evoked by local electrical stimulation of probe O, which appeared to be located in an area that has also been associated with visual motion processing with fMRI, and termed LIP (Brandt et al., 1999). The neural correlates of activation in this structure and its primate homologue are poorly understood.

Parietal Lobe

Parietal sites also generally responded to the probe and feedback stimuli. Often it appeared that fewer oscillations might be present to these stimuli, in particular to the feedback stimuli. However, this was difficult to confirm because of signal:noise considerations: parietal responses are often small and require substantial averaging, but six times as many trials were available by combining across input stimuli I1–I6 as compared to the probe or feedback stimuli. For example, in the left inferior post-central sulcus (probe P′) (Fig. 6), focal and/or polarity-inverting components from ∼200 to 500 ms were evoked by the probe stimuli. These resembled those evoked by the input stimuli, but had smaller amplitudes. The feedback stimuli also evoked similar waveforms, except they were smaller and of earlier latency, corresponding to the shorter latencies often observed in the auditory modality. Similarly, the supramarginal site shown in Figure 9 showed an enhanced late potential to the wrong feedback, catch input trials and probe stimuli.

Temporal Lobe

The fronto-parietal-occipital responses discussed above were most prominent during input stimuli I1–I6. In contrast, ventromedial temporal responses were more prominent during the probe and feedback stimuli. When considering the input stimuli, the fronto-parietal-occipital responses tended to be equal to stimuli signalling addition, subtraction or no action (‘catch trials’), whereas the ventral fronto-temporal responses tended to be greater to the catch stimuli.

Discussion

The current results showed sustained co-activation of visual processing areas with fronto-central-parietal cortices in response to simple stimuli that signalled an updating of working memory. The co-activation consisted of embedded oscillations over a wide range of frequencies from 0.1 to 40 Hz, which were observed with ERPs as well as spectral measures. These regions remained active during the entire interval until the next input stimulus, i.e. not only during the perception and interpretation of the stimulus, but also during the mental operation and updating of working memory. The participation of these areas in an extended dynamic network is suggested by the presence of task-related phase locking between their respective activities. The phase lag in the most active frequency bands between structures varied systematically after stimulus presentation, suggesting successive phases of information processing with different directions of information flow.

These findings are highly consistent with the use of the visual association cortex as a scratch pad where information is processed, held and transformed under ongoing modulations from fronto-parietal circuits. The prominent task-related oscillating of perisylvian language areas supports the hypothesized cyclical maintenance of verbal material in an ‘articulatory loop’. Finally, the strong involvement of peri-Rolandic cortices suggests that these areas may participate directly in phasic modulations during working memory.

Potentials were recorded in the lateral occipital cortex from before 100 ms to over 800 ms after the brief presentation of an input stimulus, i.e. not only during stimulus perception, but also during the entire time that the stimuli were processed arithmetically and mnestically. Local generation of these potentials was confirmed by their large amplitude and by their multiple polarity inversions between adjacent contacts separated by 1.5 mm. The location of these areas as well as their modality specificity suggest that they were typically located in visual association areas of the dorsal stream. The subjective effects of local electrical stimulation tentatively identified two such sites as corresponding to visual motion areas MT+ and LIP.

The prefrontal–premotor–parietal–dorsal occipital network observed in our study has previously been observed in fMRI and PET studies of mental arithmetic (Burbaud et al., 1999; Chochon et al., 1999; Kazui et al., 2000; Pesenti et al., 2000; Gruber et al., 2001). It has also been proposed that the haemodynamic activation observed in the left superior parietal cortex (BA7) and left anterior occipital cortex (BA19) may be related to both the spatial processing of numbers (Dehaene et al., 1996) and to a mental scanning of space during the calculation task (Burbaud et al., 1999). Our results are consistent with models where the intrinsic spatial organization of the visual association cortex, which is used at short latencies for perceptual analysis, is then put to work for more abstract mental operations (Baddeley, 1986).

Articulatory Loop

A second mechanism posited to maintain information in an active state in working memory is the ‘articulatory loop’ (Baddeley, 1986). Haemodynamic [for a review see Fiez et al. (Fiez et al., 1996)] and neuropsychological evidence indicates that internal repetition requires perisylvian language areas (Shallice and Vallar, 1990). The current results showed strong activation in multiple perisylvian sites during working memory. Activation was sustained and simultaneous in perisylvian sites posterior to the central sulcus (including the postcentral sulcus and supramarginal gyrus), as well as anterior to the central sulcus (including the precentral sulcus and pars opercularis and triangularis of the inferior frontal gyrus). The most prominent oscillations at the period of the ISI were found in the left postcentral sulcus and the supramarginal gyrus. Such oscillations imply a cycling of neuronal processing that occurs once for every stimulus, as might be expected for cyclic internal repetition. Consistent with this interpretation, the oscillation clearly begins prior to each stimulus presentation, suggesting an endogenous process rather than one that is stimulus evoked.

Material Specificity

In one version of the task administered here the memoranda to be modified and later recalled were numbers, whereas in another they were simple figures. These tasks used identical input stimuli and were identical in such formal features as timing and behavioural response. It seems reasonable to expect that figural memoranda would be processed in working memory using the visuospatial scratch pad, whereas verbal memoranda would be processed using the articulatory loop. Indeed, in the current study the perisylvian oscillations with the period of the ISI were somewhat larger when the memoranda were letters than when they were figures. However, both perisylvian and visual association areas were clearly activated by both tasks.

It is conceivable that some subjects may have adopted a method for translating figure changes into verbal labels and stored those verbal labels in the figures task. Conversely, some subjects may have devised a strategy of translating number memoranda into spatial positions. However, the nature of the task would render such strategies inordinately difficult and no subject reported having done so. Thus, the evidence suggests that both slave systems may be engaged by the central executive in order to satisfy the difficult interactions between perception, memory and processing required by the current task.

Other neuroimaging studies have had mixed success in finding material-specific activation in working memory (Owen, 1997; Ungerleider et al., 1998), thereby suggesting that such differences can sometimes be due to confounding differences in processing complexity. In the current study the memoranda were relatively simple, whereas the processing demands were difficult and equivalent across materials. Thus, differences related to material specificity might have been minimized. The relative lack of difference between verbal and figural versions of the task in our study is consistent with the scalp ERP results of an earlier study (Gevins et al., 1996), which used an n-back paradigm.

Peri-Rolandic Cortex

It was surprising to find locally generated peri-Rolandic potentials during the input period, given that the stimuli were visual and required no motor response. These potentials arrived early (∼130 ms after stimulus onset) and stayed until the next stimulus presentation. Most commonly, the ERPs oscillated rapidly, but slower activity was also present. Although the potentials recorded in the precentral, central and postcentral sulci were small (usually ∼10–30 μV), their spatial patterns exhibited clear evidence for local generation. Polarity inversions were repeatedly demonstrated between electrode contacts separated by 1.5 mm. In some cases, multiple inversions over a single trajectory were noted. Such ‘quadripolar’ configurations are not biophysically possible unless locally generated (Nunez, 1981). Structural MRI as well as complex motor phenomena evoked by local electrical stimulation (Penfield and Jasper, 1954; Chauvel et al., 1996b) confirmed the location of some of these leads in the premotor cortex. These observations are consistent with the findings of metabolic (Swartz et al., 1995) and haemodynamic (Fiez et al., 1996) activation in working memory tasks in the premotor cortex in the region of the precentral sulcus. Premotor and precentral activation have also been observed in mental arithmetic tasks, where they have been interpreted as reflecting motor responses associated with covert subvocalization of the answer (Dehaene et al., 1996). However, activation may remain in these areas after matching for difficulty and stimulus response characteristics (Dehaene et al., 1999). The current study demonstrates activation in motor areas from a very early latency to input stimuli that require no response. Thus, they are highly unlikely to reflect subvocalization.

The primary motor cortex also generated sustained potentials lasting the entire ∼6 s from the first input stimulus until after the probe. These potentials resemble the CNV that is commonly viewed at the scalp during the delay period of delayed-match-to-sample (DMS) tasks and, thus, has been proposed as reflecting sustained information-specific firing, i.e. the neural substrate of primary memory. Several authors have previously recorded the CNV intracranially, in particular in central and prefrontal sites (Papakostopoulos and Crow, 1976; Lamarche et al., 1995; Ikeda et al., 1996; Hamano et al., 1997) and lesions of the prefrontal cortex are associated with decreases in the scalp CNV (Rosahl and Knight, 1995). However, the current study appears to be the first demonstration of inversion of the CNV in humans over a short distance. This inversion was in cortex that anatomically and functionally was demonstrated to lie in the primary motor cortex for the left mouth and tongue. However, sustained potentials were also recorded in widespread cortical areas. This may correspond to the finding that sustained firing during DMS is widespread in primates (Fuster, 1989; Chafee and Goldman-Rakic, 1998) including humans (Halgren et al., 1978). Overall, the current results support involvement of the peri-Rolandic cortex in all phases of mental arithmetic and other working memory tasks rather than a limited role in response generation.

Comparison with Declarative Memory

The intracranial potentials evoked in a variety of language, memory and simple signal detection tasks have been extensively described (Halgren et al., 1980, 1994a,Halgren et al., b, 1995a,Halgren et al., b; Smith et al., 1986; McCarthy et al., 1989, 1995; Baudena et al., 1995). Such recordings in memory studies have concentrated on declarative or implicit memory tasks for complex stimuli such as words and faces. The major activation in these studies is in the ventral occipito-temporal, ventromedial temporal and ventrolateral prefrontal cortices, peaking at ∼200, 400 and 600 ms after stimulus onset. These results have been confirmed with MEG/ fMRI in normal subjects (Dale et al., 2000) and are thought to reflect sequential material-specific encoding, semantic interpretation, cognitive integration and contextual closure within a ventral event-encoding stream (Halgren and Smith, 1987).

Little activation in these ventral stream structures was noted in this study to the input stimuli, when the working memory processes are strongly engaged. Rather, medial temporal activation was most prominent to feedback stimuli indicating response correctness. Even more consistent activation to feedback was found in a related limbic site, the anterior cingulate gyrus. This finding confirms the putative function of this area in monitoring for errors (Carter et al., 2000). Furthermore, the location of this potential tends to confirm the origin of the event-related negativity that has previously been hypothesized based upon scalp recordings (Gehring and Knight, 2000).

In striking contrast to the mainly ventromedial activation in the previous declarative memory studies, activation during the input period in the current study was mainly dorsolateral, in the fronto-central-parietal cortices. The ventral activation in previous studies compared to the dorsal activation in the current study argues that the declarative and working memory systems are substantially segregated, associated respectively with a ventral stream for event-encoding integration and a dorsal stream for attention-intensive sensorimotor interactions. In the former, a complex meaningful stimulus is subjected to material-specific encoding, related to semantic, emotional and episodic memories of different ages, and then integrated with the current cognitive context. In contrast, the dorsal stream may involve much simpler stimuli, allowing rapid interpretation, but at a more shallow level. This path is required when there is rapid switching of attentional or processing resources between different stimuli or processing modes, even (or perhaps particularly) when those stimuli or processes are each simple when considered individually.

It is interesting in this context to note that working memory has a strong correlation with the psychometric construct of general intelligence or ‘g’ (Kyllonen and Christal, 1990), whereas declarative memory has only a weak relationship and indeed can be completely dissociated in amnesia (Corkin, 1984). The original Mental Counters task correlates strongly with Raven's Progressive Matrices (r = 0.59), the standard psychometric test generally accepted to correlate most strongly with g (Larson and Saccuzzo, 1989), We confirmed that our Mental Counters variant that was most similar to Larson's original task (N2V) (Larson and Saccuzzo, 1989) also correlated significantly (P < 0.01) with Raven's Progressive Matrices (r = 0.51) in a study of 55 normal subjects. The finding that distinct areas are activated in working versus declarative memory tasks is consistent with their psychometric and neuropsychological dissociations, and furthermore suggests that g is most closely associated with activity in the dorsal parieto-frontal stream (Duncan and Owen, 2000).

Spectral Activation

The current study found that ERPs in sensory and motor areas as well as the posterior and anterior association cortices were simultaneously active during all phases of a complex working memory task: perception, interpretation, retrieval, calculation and storage. This finding was confirmed by spectral analysis of SEEG from single trials. The increase in spectral power includes both the lower frequencies observed in the ERPs (<∼12 Hz), as well as higher frequencies (up to ∼50 Hz, the limits of the recordings). This broadband increase confirms and extends the implication of ERPs that multiple sites are simultaneously active during the Mental Counters task.

The frontal midline theta rhythm in scalp EEG has been observed in a number of tasks that require sustained mental effort and particularly during mental arithmetic (Inanaga, 1998; Klimesch, 1999). The scalp topography of this rhythm can be modelled as either resulting from a single equivalent current dipole in the anterior cingulate cortex (Gevins et al., 1997) or from diffusely distributed cortical activity. The current results clearly found multiple diffusely distributed generators of these rhythms, with only a minor contribution from the anterior cingulate cortex. This is consistent with the widespread theta band task-related oscillations recorded with intracranial grid electrodes during the retention period of the Sternberg paradigm (Raghavachari et al., 2001), as well as during a spatial maze task (Caplan et al., 2001).

Much discussion has centred on the role of oscillations in the gamma range for integrating activity in large cortical networks (Singer, 1999; Tallon-Baudry and Bertrand, 1999; Varela et al., 2001). In our study, activation in the theta and alpha bands was more common. Gamma activation occurred primarily in early visual or primary motor regions, where indeed most of the evidence for a role of gamma activity has been obtained (Crone et al., 1998, 2001; Aoki et al., 2001). Broadband increases have also been noted in the visual cortex of macaques (Young et al., 1992; Victor et al., 1994). In humans, faces evoke increased fusiform spectral power from theta to gamma, whereas the spectral increase in the ventrolateral prefrontal cortex is limited to the theta and alpha bands (Klopp et al., 1999). Overall, these results suggest that phasic broadband activation may be characteristic of sensory and motor cortex, whereas long-lasting theta activation may characterize higher association cortex during complex tasks.

Occipital alpha activity decreases to visual stimulation (Berger, 1929), as does the central ‘mu’ rhythm (Hari and Salmelin, 1997; Klopp et al., 2001). It is thought that these ‘resting rhythms’ are inversely related to the amount of cortical resources allocated to task performance (Pfurtscheller et al., 1996; Smith et al., 1999). In the current study, spectral power in a given electrode contact and frequency band would often show a phasic increase at the time of presumed maximal functional involvement, on the background of a sustained decrease relative to baseline. This suggests that the same oscillatory mode may be engaged during activation as during rest. Similarly, although alpha overall decreases in the human fusiform gyrus to faces, it strongly increases at ∼200 ms, when it appears to make its specific contribution to face encoding (Klopp et al., 1999). Preferred oscillatory modes emerge from the intrinsic membrane properties of neurons, as well as their connectivity, conduction and synaptic delays (Freeman, 1978; Connors and Amitai, 1997; Steriade, 1998; Nunez, 2000). These data suggest that the alpha and mu rhythms may represent preferred oscillatory modes that may be entered during either activation or inactivation. More information would be passed through the activated system due to a higher background level of excitation, but it would be passed at the same preferred frequency.

Interareal Interactions

The current study tested for possible interactions between simultaneously activated structures by examining the task-related similarities in their SEEGs in each trial on a millisecond time-scale for every frequency band. Most previous studies using these measures to study interactions between cortical areas in humans have relied on scalp EEG recordings (Tallon-Baudry and Bertrand, 1999). However, such measures are difficult to interpret because of spatial blurring caused by signal super-position and intervening tissues, as well as possible extracranial sources (Pfurtscheller and Cooper, 1975; Srinivasan et al., 1998). Furthermore, the information present in relatively low frequency phase locking is poorly suited for the temporal coding of cell assemblies (Shadlen and Movshon, 1999).

When applied to SEEG, spectral coherence or phase locking directly measure the similarity of local synaptic current fluctuations between different areas and, thus, can imply their interaction and communication. Such measures do not necessarily imply that these areas are directly connected, but could be due to a common input from a third structure. However, at least in macaques, multiple direct as well as indirect anatomical connections seem to be present between all of the relevant structures. In addition to the many, shared connections between intraparietal and dorsolateral prefrontal cortices (Goldman-Rakic, 1988; Selemon and Goldman-Rakic, 1988), connections also exist linking these structures to area MT+ and the precentral and premotor cortices (Barbas and Pandya, 1987; Cavada and Goldman-Rakic, 1989; Boussaoud et al., 1990; Wise et al., 1997). Furthermore, these cortico-cortical connections are highly likely to be excitatory (Salin and Bullier, 1995; Somogyi et al., 1998). Given these neuroanatomical data showing multiple connections between the structures with task-related correlated activity, the current results strongly support the active interaction of these structures during working memory in humans.

Although some prior studies in mammals with unit firing and in humans with scalp EEG have suggested that synchrony between areas is predominantly in the gamma band (Rodriguez et al., 1999; Singer, 1999; Tallon-Baudry and Bertrand, 1999), the current study found that task-related phase-locking increases are present in several frequency bands, from 4 to ∼40 Hz. This corresponds to several studies in behaving macaques that have found broadband coherence increases between field potentials or multi-unit activity in different cortical structures (Bressler, 1995, 1996; Salin and Bullier, 1995; Sakurai, 1996). These observations are also consistent with the EEG data of Von Stein and Sarnthein (Von Stein and Sarnthein, 2000) who found local coherence increases between visual areas in the gamma range, whereas fronto-parietal interactions during working memory retention were in the theta and alpha bands. A broadband increase in coherence was also found in human SEEG between the fusiform face area and widespread cortical regions during face recognition, peaking at ∼200 ms (Klopp et al., 2000). The phase lead of the fusiform gyrus increased linearly with distance, suggesting transmission of specific encoding information from the fusiform gyrus to widespread cortical areas. In the current study, similar circumstantial evidence for the transmission of information between cortical areas could be inferred from the consistent pattern of interareal phase lags.

By combining these phase lag data with phase-locking, spectral power and ERP data it is possible to discern several neurophysiological stages during the processing of input stimuli in this difficult working memory task. These effects are stable for ∼100 ms and then shift to another pattern, as one might expect if there were multiple information processing stages invoking distinct patterns of synaptic activity and information flow. Combined with the neuropsychological, neuroanatomical and neuroimaging results reviewed above, these data tentatively suggest that the following neurocognitive stages are engaged by the Mental Counters task: (i) initial perceptual processing exclusively in the visual association cortex from ∼90 to 130 ms; (ii) identification, where the results of perceptual processing are projected to fronto-parietal areas for interpretation from ∼130 to 280 ms; (iii) calculation performed by fronto-parietal areas operating upon the occipital scratch pad from ∼300 to 400 ms; and (iv) updating of working memory, where the results of the calculation are projected from occipital to fronto-parietal sites from ∼420 to 600 ms in preparation for the next stimulus. The suggested cognitive functions of these successive stages are speculative. Regardless of whether they are confirmed by future experiments, the current results clearly imply that difficult working memory tasks are performed in humans by a continuous interaction of multiple cortical areas in the occipital, parietal, central and frontal cortices.

Table 1

Behavioural performance

Correct positive Correct rejection Miss False positive No response
RT RT RT RT
N2V, two number memoranda with visual presentation (16 subjects); F2V, two figural memoranda with visual presentation (10 subjects).
N2V mean 39 999 34 1163 10 1296 14 1149
N2V SD 266 255 416 450
F2V mean 36 948 29 1145 12 1070 18 1037
F2V SD 10 166 10 187 398 243
Correct positive Correct rejection Miss False positive No response
RT RT RT RT
N2V, two number memoranda with visual presentation (16 subjects); F2V, two figural memoranda with visual presentation (10 subjects).
N2V mean 39 999 34 1163 10 1296 14 1149
N2V SD 266 255 416 450
F2V mean 36 948 29 1145 12 1070 18 1037
F2V SD 10 166 10 187 398 243
Figure 1.

The Mental Counters task. Examples of two variants of mental counters are shown. Other variants using three locations or letters as memoranda were also used, as described in the text.

Figure 1.

The Mental Counters task. Examples of two variants of mental counters are shown. Other variants using three locations or letters as memoranda were also used, as described in the text.

Figure 2.

Electrode locations. The probe entry points in the left and right hemispheres (LH and RH) are normalized following an earlier study (Talairach and Tournoux, 1988). Recording contacts are located every 3.5 mm (centre to centre) along the probe's lateral to medial trajectory orthogonal to the sagittal plane.

Figure 2.

Electrode locations. The probe entry points in the left and right hemispheres (LH and RH) are normalized following an earlier study (Talairach and Tournoux, 1988). Recording contacts are located every 3.5 mm (centre to centre) along the probe's lateral to medial trajectory orthogonal to the sagittal plane.

Figure 3.

Sustained co-activation of the occipital, parietal and Rolandic cortices. Each set of waveforms shows activity recorded from one of 26 different contacts located on five probes recorded simultaneously from a subject performing the Mental Counters task. Each recording begins 40 ms before and ends 800 ms after stimulus onset. Activity is maintained simultaneously in occipital, parietal, central and medial sites for much of the trial. In the upper traces, multiple inversions in polarity are recorded from ∼100 to 800 ms by two anterior occipital probes (O and D) (the numbers indicate the distance in millimetres from the centre of the recording contact to the cerebral midline). Several components peaking from 105 to 760 ms post-stimulus in probe D (upper right column) gradually increase in amplitude as the probe passes from the deep white matter (contact D28) into the fundus of the anterior occipital sulcus (aOs) (contact D35). Large potentials with multiple inversions are seen in contacts D38–D52 as the probe passes first through the anterior bank of the sulcus (i.e. the most posterior part of the middle temporal gyrus or mTg) and then the posterior bank (i.e. the most anterior part of the middle occipital gyrus or mOg). The earlier peaks at ∼105 and 180 ms invert more medially (○) than do later peaks at ∼320, 500 and 680 ms (△). The internal contacts of probe O (left column) are in the right superior parietal lobule (sPl) at its junction with the superior occipital gyrus and the external contacts are in the inferior parietal lobule (iPl) at its junction with the middle occipital gyrus. Multiple large peaks are seen to polarity invert between contacts O25, O29 and O32, for example at ∼200 ms (•). These contacts lie in the fundus of the intraparietal sulcus (iPs) at its limit with the superior occipital sulcus. The rapid oscillations in contacts D35–42 and O25–29 are superimposed on a slower oscillation with a period approximately equal to the ISI (✶, m). Localization of the responsive contacts in visual motion areas was confirmed by the subjective illusions of head movement evoked by electrical stimulation between contacts D38 and D42 and between contacts O22 and O25 (1 s and 2.5 mA). In the lower traces, potentials in the same latency range are shown from probes passing through the parietal, cingulate and Rolandic cortices. The deepest contacts (P4–P11) in the cingulate sulcus (Cis) record a small but polarity-inverting N200 (⋄). The probe then passes though the white matter of the superior parietal lobule (contact P28) where it records slowly changing N200–P275–N360–P440 components (△, H), which change morphology and then polarity invert as the probe enters the fundus of the most anterior part of the intraparietal sulcus (contacts P32–P39). The recordings again stabilize as the electrode passes through the grey matter of the inferior parietal lobule (contacts P42–P46), with a final low-amplitude inversion at the most lateral contact (P53) in the external grey matter of the superior limit of the inferior parietal lobule (□). Polarity inversions of what appear to be the same components (⋄) are also recorded by contacts S53–S60 in the supramarginal gyrus (sMg) (the anterior bank of the ascending ramus of the lateral fissure; see the coronal MRI in Fig. 5) and similar potentials are recorded in the central sulcus (Ces) (G55; see Fig. 8 for MRI), as well as by other contacts in the cingulate sulcus (S18 and G13). The three waveforms in each set represent the activation evoked by Mental Counters' variants differing in the material memorized (numbers, letters or figures). No significant material-specific differences are visible. x/y/z coordinates (Talairach and Tournoux, 1988) of the probes (actual followed by normalized): probe D (28–45/–71/14 and 27–44/–75/15), probe O (15–36/–79/30 and 15–35/–84/32), probe P (4–53/–39/54 and 4–52/–41/58), probe S (18–60/–29/35 and 18–59/–31/37) and probe G (55/–10/39 and 57/–11/42). See Figure 5 for electrode localization. Pt. 2.

Sustained co-activation of the occipital, parietal and Rolandic cortices. Each set of waveforms shows activity recorded from one of 26 different contacts located on five probes recorded simultaneously from a subject performing the Mental Counters task. Each recording begins 40 ms before and ends 800 ms after stimulus onset. Activity is maintained simultaneously in occipital, parietal, central and medial sites for much of the trial. In the upper traces, multiple inversions in polarity are recorded from ∼100 to 800 ms by two anterior occipital probes (O and D) (the numbers indicate the distance in millimetres from the centre of the recording contact to the cerebral midline). Several components peaking from 105 to 760 ms post-stimulus in probe D (upper right column) gradually increase in amplitude as the probe passes from the deep white matter (contact D28) into the fundus of the anterior occipital sulcus (aOs) (contact D35). Large potentials with multiple inversions are seen in contacts D38–D52 as the probe passes first through the anterior bank of the sulcus (i.e. the most posterior part of the middle temporal gyrus or mTg) and then the posterior bank (i.e. the most anterior part of the middle occipital gyrus or mOg). The earlier peaks at ∼105 and 180 ms invert more medially (○) than do later peaks at ∼320, 500 and 680 ms (△). The internal contacts of probe O (left column) are in the right superior parietal lobule (sPl) at its junction with the superior occipital gyrus and the external contacts are in the inferior parietal lobule (iPl) at its junction with the middle occipital gyrus. Multiple large peaks are seen to polarity invert between contacts O25, O29 and O32, for example at ∼200 ms (•). These contacts lie in the fundus of the intraparietal sulcus (iPs) at its limit with the superior occipital sulcus. The rapid oscillations in contacts D35–42 and O25–29 are superimposed on a slower oscillation with a period approximately equal to the ISI (✶, m). Localization of the responsive contacts in visual motion areas was confirmed by the subjective illusions of head movement evoked by electrical stimulation between contacts D38 and D42 and between contacts O22 and O25 (1 s and 2.5 mA). In the lower traces, potentials in the same latency range are shown from probes passing through the parietal, cingulate and Rolandic cortices. The deepest contacts (P4–P11) in the cingulate sulcus (Cis) record a small but polarity-inverting N200 (⋄). The probe then passes though the white matter of the superior parietal lobule (contact P28) where it records slowly changing N200–P275–N360–P440 components (△, H), which change morphology and then polarity invert as the probe enters the fundus of the most anterior part of the intraparietal sulcus (contacts P32–P39). The recordings again stabilize as the electrode passes through the grey matter of the inferior parietal lobule (contacts P42–P46), with a final low-amplitude inversion at the most lateral contact (P53) in the external grey matter of the superior limit of the inferior parietal lobule (□). Polarity inversions of what appear to be the same components (⋄) are also recorded by contacts S53–S60 in the supramarginal gyrus (sMg) (the anterior bank of the ascending ramus of the lateral fissure; see the coronal MRI in Fig. 5) and similar potentials are recorded in the central sulcus (Ces) (G55; see Fig. 8 for MRI), as well as by other contacts in the cingulate sulcus (S18 and G13). The three waveforms in each set represent the activation evoked by Mental Counters' variants differing in the material memorized (numbers, letters or figures). No significant material-specific differences are visible. x/y/z coordinates (Talairach and Tournoux, 1988) of the probes (actual followed by normalized): probe D (28–45/–71/14 and 27–44/–75/15), probe O (15–36/–79/30 and 15–35/–84/32), probe P (4–53/–39/54 and 4–52/–41/58), probe S (18–60/–29/35 and 18–59/–31/37) and probe G (55/–10/39 and 57/–11/42). See Figure 5 for electrode localization. Pt. 2.

Figure 6.

Sustained activations and interactions in the peri-Rolandic cortex. Pt. 9 spectra (top). Event-related spectral time–frequency plots were calculated on individual trials and then summed and normalized with respect to the baseline period, for sites in the primary motor (R), premotor (M) and prefrontal (K and F) cortices. Spectral power (left) is plotted continuously over the entire trial (upper left), consisting of six input stimuli (I1–I6), the answer probe (P) and response/feedback (F), as well as collapsed across the input stimuli (I1–I6 at top middle). The most consistent spectral changes are in the theta and low alpha bands from ∼300 to 400 ms (vertical grey stripes). These changes include increases in spectral power (□) and phase locking (△ at upper right). Activity in the prefrontal cortex (K49) tends to lead other sites during this epoch (upward open arrow). In addition, a high frequency response (45–50 Hz) is present in K49 (○). During the preceding epoch (∼150–280 ms) (vertical tan stripes), spectral activation tends to be in the high alpha and beta range (⋄) and other sites tend to lead the premotor cortex (M35) (downward open arrows). Pt. 9 waveforms (middle left). ERPs from ∼130 to 600 ms are recorded from two probes (K and M) passing through the precentral sulcus (preCs). Multiple inversions are seen between adjacent contacts separated by 1.5 mm: an N160/N210 complex in K46 inverts to a P170/P220 in K49 (○-arrows) and an N230 in M28 inverts to a P230 in M31 (•). Additional small non-inverting negativities in the 400–500 ms range are also seen. Note that, as in the postcentral cortex, these responses are small (∼25 μV), but the inversions are very clear. Similar responses are seen to stimuli that evoke addition, subtraction or no operation, and that lead to updating numerical versus figural memoranda (N2I versus F2I). Electrical stimulation (2–5 mA, 20 pulses/s and 2.5 s) of M28–M31 and M31–M35 provoked a discrete fall of the left arm and flexion of digits in the left hand. Together with the anatomical location, these results indicate that M28–M35 are located in the premotor cortex. Stimulation (1 pulse/s) of R28–31 evoked contractions of the left hand and fingers, and of R31–34 evoked contractions of the eyelids, confirming localization in the primary motor cortex. Stimulation of K42–K49 and of F23–F30 provoked no response. Probe coordinates (actual followed by normalized): probe M (28–35/3/62 and 28–35/3/70), probe K (46–49/12/36 and 46–49/12/40), probe F (26/32/31 and 26/32/35) and probe R (31/–7/41 and 31/–7/46). Pt. 13 (lower left). A series of potentials in the same latency range polarity inverting over short distances, this time in the postcentral sulcus (posCs). Components at ∼210 and ∼265 ms invert between S33 and S36 (△), again between S40 and S43 (□) and possibly again between S47 and S50 (✶). An earlier potential (peaking at ∼180 ms) as well as later potentials (at ∼360 and 500 ms), which do not invert, are also seen. Stimulation of S22–S26 (21–24) (1.5 mA) provoked a feeling of a painful electrical discharge in the left hand, stimulation of S33–S36 (1.5 mA) provoked shivers in both palms and stimulation of S40–S43 (1.5 mA) provoked no subjective response. Interictal EEG recorded by probe S was within normal limits and the patient's seizures were found to arise in the temporal lobe, without spread to electrode S. Probe coordinates (actual followed by normalized): probe S (33–50/–23/35 and 30–46/–25/34). Pt. 14 (right). Recordings in the left postcentral sulcus show an extended activation, with peaks at ∼200 and 450 ms. The latter peak is large (60 μV) and inverts polarity between P′52 and P′59 (H-arrows). This response is larger to stimuli that direct the updating of numerical (⋄) (N2I) as compared to figural (•) (F2I) memoranda. Similar, but smaller responses are recorded to response probe stimuli (h-arrows) (N2P). Feedback stimuli (h-arrows) (N2F) also evoke similar waveforms, but at ∼70–100 ms shorter latencies. Probe coordinates (actual followed by normalized): probe P′ (–49 to 59/–14/27 and –47 to 57/–14/26).

Figure 6.

Sustained activations and interactions in the peri-Rolandic cortex. Pt. 9 spectra (top). Event-related spectral time–frequency plots were calculated on individual trials and then summed and normalized with respect to the baseline period, for sites in the primary motor (R), premotor (M) and prefrontal (K and F) cortices. Spectral power (left) is plotted continuously over the entire trial (upper left), consisting of six input stimuli (I1–I6), the answer probe (P) and response/feedback (F), as well as collapsed across the input stimuli (I1–I6 at top middle). The most consistent spectral changes are in the theta and low alpha bands from ∼300 to 400 ms (vertical grey stripes). These changes include increases in spectral power (□) and phase locking (△ at upper right). Activity in the prefrontal cortex (K49) tends to lead other sites during this epoch (upward open arrow). In addition, a high frequency response (45–50 Hz) is present in K49 (○). During the preceding epoch (∼150–280 ms) (vertical tan stripes), spectral activation tends to be in the high alpha and beta range (⋄) and other sites tend to lead the premotor cortex (M35) (downward open arrows). Pt. 9 waveforms (middle left). ERPs from ∼130 to 600 ms are recorded from two probes (K and M) passing through the precentral sulcus (preCs). Multiple inversions are seen between adjacent contacts separated by 1.5 mm: an N160/N210 complex in K46 inverts to a P170/P220 in K49 (○-arrows) and an N230 in M28 inverts to a P230 in M31 (•). Additional small non-inverting negativities in the 400–500 ms range are also seen. Note that, as in the postcentral cortex, these responses are small (∼25 μV), but the inversions are very clear. Similar responses are seen to stimuli that evoke addition, subtraction or no operation, and that lead to updating numerical versus figural memoranda (N2I versus F2I). Electrical stimulation (2–5 mA, 20 pulses/s and 2.5 s) of M28–M31 and M31–M35 provoked a discrete fall of the left arm and flexion of digits in the left hand. Together with the anatomical location, these results indicate that M28–M35 are located in the premotor cortex. Stimulation (1 pulse/s) of R28–31 evoked contractions of the left hand and fingers, and of R31–34 evoked contractions of the eyelids, confirming localization in the primary motor cortex. Stimulation of K42–K49 and of F23–F30 provoked no response. Probe coordinates (actual followed by normalized): probe M (28–35/3/62 and 28–35/3/70), probe K (46–49/12/36 and 46–49/12/40), probe F (26/32/31 and 26/32/35) and probe R (31/–7/41 and 31/–7/46). Pt. 13 (lower left). A series of potentials in the same latency range polarity inverting over short distances, this time in the postcentral sulcus (posCs). Components at ∼210 and ∼265 ms invert between S33 and S36 (△), again between S40 and S43 (□) and possibly again between S47 and S50 (✶). An earlier potential (peaking at ∼180 ms) as well as later potentials (at ∼360 and 500 ms), which do not invert, are also seen. Stimulation of S22–S26 (21–24) (1.5 mA) provoked a feeling of a painful electrical discharge in the left hand, stimulation of S33–S36 (1.5 mA) provoked shivers in both palms and stimulation of S40–S43 (1.5 mA) provoked no subjective response. Interictal EEG recorded by probe S was within normal limits and the patient's seizures were found to arise in the temporal lobe, without spread to electrode S. Probe coordinates (actual followed by normalized): probe S (33–50/–23/35 and 30–46/–25/34). Pt. 14 (right). Recordings in the left postcentral sulcus show an extended activation, with peaks at ∼200 and 450 ms. The latter peak is large (60 μV) and inverts polarity between P′52 and P′59 (H-arrows). This response is larger to stimuli that direct the updating of numerical (⋄) (N2I) as compared to figural (•) (F2I) memoranda. Similar, but smaller responses are recorded to response probe stimuli (h-arrows) (N2P). Feedback stimuli (h-arrows) (N2F) also evoke similar waveforms, but at ∼70–100 ms shorter latencies. Probe coordinates (actual followed by normalized): probe P′ (–49 to 59/–14/27 and –47 to 57/–14/26).

Figure 7.

Widespread embedded fronto-parieto-temporal oscillations. Pt. 14 (left). The potentials recorded across an entire trial consisting of warning (W), six input stimuli (I1–I6), response probe (P) and feedback (F). Strong oscillations begin with the warning stimulus in the left inferior postcentral sulcus (P′52) and continue through the input stimuli (h, △). Weaker oscillatory responses are also present in Broca's area (posterior inferior frontal gyrus or piFg) (R′60) where the response is more prominent to the response probe than to the warning. The oscillatory response is weaker in the probe anterior to Broca's area (I'42). Both the prefrontal and parietal responses are larger to stimuli signalling change to numerical memoranda (N2) than identical stimuli signalling updates of figural memoranda (F2). Stimulation (1.5 mA) of R′57–R′60 and adjacent contacts caused an immediate arrest of reading and/or paraphasias. Stimulation of I′42–I′45 (2.5 mA) only evoked paraphasia when it also provoked a seizure that spread to R′60. Thus, R′60 lies in Broca's area according to stimulation and I′42 probably lies immediately anterior to it. Note that, since the time from the probe to the feedback was not constant, ‘FB’ is written at the average time. Probe coordinates (actual followed by normalized): probe R′ (–60/11/15 and –57/11/14) and probe I′ (–42/26/7 and –39/26/7). Pt. 10 (right upper). Slow oscillations recorded below the left superior temporal sulcus (sTs) (C'56). Probe coordinates (actual followed by normalized): probe C′ (–56/–27/–8.5 and –56/–26/–9). Pt. 13 (right lower). Slow oscillations recorded below the right superior temporal sulcus (D61) and, in particular, in the supramarginal gyrus (sMg) (P52) (H, △). Like the postcentral sulcus response, the supramarginal gyrus response clearly begins to the warning stimulus. Probe coordinates (actual followed by normalized): probe D (61/–62/14 and 61/–68/14) and probe P (52/–40/31 and 48/–44/31).

Figure 7.

Widespread embedded fronto-parieto-temporal oscillations. Pt. 14 (left). The potentials recorded across an entire trial consisting of warning (W), six input stimuli (I1–I6), response probe (P) and feedback (F). Strong oscillations begin with the warning stimulus in the left inferior postcentral sulcus (P′52) and continue through the input stimuli (h, △). Weaker oscillatory responses are also present in Broca's area (posterior inferior frontal gyrus or piFg) (R′60) where the response is more prominent to the response probe than to the warning. The oscillatory response is weaker in the probe anterior to Broca's area (I'42). Both the prefrontal and parietal responses are larger to stimuli signalling change to numerical memoranda (N2) than identical stimuli signalling updates of figural memoranda (F2). Stimulation (1.5 mA) of R′57–R′60 and adjacent contacts caused an immediate arrest of reading and/or paraphasias. Stimulation of I′42–I′45 (2.5 mA) only evoked paraphasia when it also provoked a seizure that spread to R′60. Thus, R′60 lies in Broca's area according to stimulation and I′42 probably lies immediately anterior to it. Note that, since the time from the probe to the feedback was not constant, ‘FB’ is written at the average time. Probe coordinates (actual followed by normalized): probe R′ (–60/11/15 and –57/11/14) and probe I′ (–42/26/7 and –39/26/7). Pt. 10 (right upper). Slow oscillations recorded below the left superior temporal sulcus (sTs) (C'56). Probe coordinates (actual followed by normalized): probe C′ (–56/–27/–8.5 and –56/–26/–9). Pt. 13 (right lower). Slow oscillations recorded below the right superior temporal sulcus (D61) and, in particular, in the supramarginal gyrus (sMg) (P52) (H, △). Like the postcentral sulcus response, the supramarginal gyrus response clearly begins to the warning stimulus. Probe coordinates (actual followed by normalized): probe D (61/–62/14 and 61/–68/14) and probe P (52/–40/31 and 48/–44/31).

Figure 8.

Widespread CNV-like potentials and embedded oscillations. Pt. 2 (left). Oscillating activations at different time-scales are seen in different simultaneously recorded contacts in occipital, parietal and central sites. Phasic responses lasting 50–100 ms are seen in the supramarginal gyrus (⋄; S53), anterior intraparietal sulcus (△; P39–P42), posterior intraparietal sulcus (•; O25–O29) and central sulcus (G41–G48). These responses often habituate to successive input stimuli (⋄, △, ○). For example, in contact S53 the N210–P280 declines from ∼85 μV to I1 (⋄), ∼65 μV to I2 (⋄), ∼55 μV to I3 and ∼45 μV to I4–I6. Similarly, the P280 in P39 declines from ∼65 μV to I1 (△), to ∼45 μV to I2 (△) and ∼25 μV to subsequent stimuli. A later component at ∼500 ms also declines from ∼40 to ∼20 μV over the same period. Finally, in G48 the N210–P290 peak to peak measure strongly declines in amplitude from 50 μV to I1 to 10–20 μV to succeeding stimuli. A weaker habituation of ∼40% occurs in contacts G41 and G44. A dual-peaked response with an overall periodicity equal to the input stimulus ISI of 960 ms inverts between O25 and O29 in the posterior intraparietal sulcus. Polarity inversion is particularly clear for the earlier peak at ∼220 ms (h). Habituation across successive stimuli in a trial is prominent in the later peak at ∼350 ms, with baseline to peak values declining from ∼110 μV to I1 (•) to ∼65 μV to I3–I6 (○). Finally, although sustained responses lasting ∼6 s are seen in several leads (e.g. P39), it is largest and polarity inverts between the grey matter of the precentral gyrus (G44) and the central sulcus (G48) (H), according to the MRI (lower right). Direct electrical stimulation between contacts G41–G44 evoked left mouth and tongue twitches. See Figure 5 for additional electrode locations. Pt. 7 (right upper). Long-duration potentials in another patient are recorded in the left anterior cingulate sulcus (R′21), where the potential is negative and in the vicinity of the H-shaped orbital sulcus (O′15), where it is positive. Note the rapid habituation of the P290 in the cingulate sulcus (□, □). Probe coordinates (actual followed by normalized): probe R′ (–21/36/–20 and –20/41/–20) and probe O′ (–15/–10/47 and –15/–11/46).

Widespread CNV-like potentials and embedded oscillations. Pt. 2 (left). Oscillating activations at different time-scales are seen in different simultaneously recorded contacts in occipital, parietal and central sites. Phasic responses lasting 50–100 ms are seen in the supramarginal gyrus (⋄; S53), anterior intraparietal sulcus (△; P39–P42), posterior intraparietal sulcus (•; O25–O29) and central sulcus (G41–G48). These responses often habituate to successive input stimuli (⋄, △, ○). For example, in contact S53 the N210–P280 declines from ∼85 μV to I1 (⋄), ∼65 μV to I2 (⋄), ∼55 μV to I3 and ∼45 μV to I4–I6. Similarly, the P280 in P39 declines from ∼65 μV to I1 (△), to ∼45 μV to I2 (△) and ∼25 μV to subsequent stimuli. A later component at ∼500 ms also declines from ∼40 to ∼20 μV over the same period. Finally, in G48 the N210–P290 peak to peak measure strongly declines in amplitude from 50 μV to I1 to 10–20 μV to succeeding stimuli. A weaker habituation of ∼40% occurs in contacts G41 and G44. A dual-peaked response with an overall periodicity equal to the input stimulus ISI of 960 ms inverts between O25 and O29 in the posterior intraparietal sulcus. Polarity inversion is particularly clear for the earlier peak at ∼220 ms (h). Habituation across successive stimuli in a trial is prominent in the later peak at ∼350 ms, with baseline to peak values declining from ∼110 μV to I1 (•) to ∼65 μV to I3–I6 (○). Finally, although sustained responses lasting ∼6 s are seen in several leads (e.g. P39), it is largest and polarity inverts between the grey matter of the precentral gyrus (G44) and the central sulcus (G48) (H), according to the MRI (lower right). Direct electrical stimulation between contacts G41–G44 evoked left mouth and tongue twitches. See Figure 5 for additional electrode locations. Pt. 7 (right upper). Long-duration potentials in another patient are recorded in the left anterior cingulate sulcus (R′21), where the potential is negative and in the vicinity of the H-shaped orbital sulcus (O′15), where it is positive. Note the rapid habituation of the P290 in the cingulate sulcus (□, □). Probe coordinates (actual followed by normalized): probe R′ (–21/36/–20 and –20/41/–20) and probe O′ (–15/–10/47 and –15/–11/46).

Figure 9.

Late occipital, parietal and hippocampal potentials to catch and probe stimuli. Small, late (peak latency ∼500 ms), negative potentials are recorded to ‘catch’ input stimuli (N2I) in the supramarginal gyrus (P47) (•) and the most posterior portion of the middle temporal gyrus (p-mTg) (O41 and O44) (□), anterior to the usual location of area MT+. The more medial contacts on the O probe (which electrical stimulation indicated were located in the retinotopic cortex) do not show this response. Potentials with the same latencies and polarity are recorded in the same sites as false probes (N2P) (△). The same potentials appear to be evoked at an earlier latency to feedback indicating incorrect responses (N2F) (⋄). An earlier latency is expected because the feedback signals are in the auditory modality. Simultaneously recorded hippocampal formation (HCF) contacts (B40) are selectively responsive to the feedback tones (h). Scalp potentials at Pz do not closely resemble any of the depth sites and are usually inverted in polarity from the posterior portion of the middle temporal gyrus and supramarginal gyrus recordings. Probe coordinates (actual followed by normalized): probe P (47/–40/30 and 48/–28/29), probe O (34–44/–59/20 and 34–45/–56/19) and probe B (40/–18/–16 and 41/–17/–16). Pt. 5.

Figure 9.

Late occipital, parietal and hippocampal potentials to catch and probe stimuli. Small, late (peak latency ∼500 ms), negative potentials are recorded to ‘catch’ input stimuli (N2I) in the supramarginal gyrus (P47) (•) and the most posterior portion of the middle temporal gyrus (p-mTg) (O41 and O44) (□), anterior to the usual location of area MT+. The more medial contacts on the O probe (which electrical stimulation indicated were located in the retinotopic cortex) do not show this response. Potentials with the same latencies and polarity are recorded in the same sites as false probes (N2P) (△). The same potentials appear to be evoked at an earlier latency to feedback indicating incorrect responses (N2F) (⋄). An earlier latency is expected because the feedback signals are in the auditory modality. Simultaneously recorded hippocampal formation (HCF) contacts (B40) are selectively responsive to the feedback tones (h). Scalp potentials at Pz do not closely resemble any of the depth sites and are usually inverted in polarity from the posterior portion of the middle temporal gyrus and supramarginal gyrus recordings. Probe coordinates (actual followed by normalized): probe P (47/–40/30 and 48/–28/29), probe O (34–44/–59/20 and 34–45/–56/19) and probe B (40/–18/–16 and 41/–17/–16). Pt. 5.

Figure 10.

Late potentials in anterior cingulate gyrus and ventral temporofrontal sites to feedback and catch stimuli. Pt. 3 (upper left). A negative potential at ∼400 ms to catch trials in the posterior inferior frontal gyrus (p-iFg) (G52) (•) is not recorded in the adjacent contact, suggesting local generation. Probe coordinates (actual followed by normalized): probe G (52/27/1 and 54/25/1). Pt. 6 (middle left). Negative potentials at ∼300 ms are recorded in the anterior cingulate gyrus (aCg) (O3) (□) to feedback tones indicating wrong responses (L2F). Probe coordinates (actual followed by normalized): probe O (3/38/–5 and 3/38/–5). Pt. 10 (lower left). Negative potentials at ∼300 ms are again recorded in the anterior cingulate gyrus (O′7) (△) to feedback indicating wrong responses (N2F). Probe coordinates (actual followed by normalized): O′ (7/45/–13 and –7/44/–12). Pt. 1 (right). Again, a potential to incorrect feedback tones is recorded in the anterior cingulate gyrus (G12) (⋄), as well as in other limbic sites including the posterior hippocampus (p-HC) (C26) (□) and the posterior parahippocampal gyrus (p-pHCg) (D24) (○). These sites all generate a positivity at ∼300 ms that resembles the simultaneous P300 recorded at the scalp (Pz) (△). The same sites showed little or no response to the input stimuli, except for the catch trials (shown only for the anterior cingulate gyrus) (G9) (⋄). Probe coordinates (actual followed by normalized): probe D (24/–45/11 and 24/–44/11), probe C (26/26/–39/–3 and 26/–38/–4) and probe G (9–12/36/2 and 9–12/36/2).

Figure 10.

Late potentials in anterior cingulate gyrus and ventral temporofrontal sites to feedback and catch stimuli. Pt. 3 (upper left). A negative potential at ∼400 ms to catch trials in the posterior inferior frontal gyrus (p-iFg) (G52) (•) is not recorded in the adjacent contact, suggesting local generation. Probe coordinates (actual followed by normalized): probe G (52/27/1 and 54/25/1). Pt. 6 (middle left). Negative potentials at ∼300 ms are recorded in the anterior cingulate gyrus (aCg) (O3) (□) to feedback tones indicating wrong responses (L2F). Probe coordinates (actual followed by normalized): probe O (3/38/–5 and 3/38/–5). Pt. 10 (lower left). Negative potentials at ∼300 ms are again recorded in the anterior cingulate gyrus (O′7) (△) to feedback indicating wrong responses (N2F). Probe coordinates (actual followed by normalized): O′ (7/45/–13 and –7/44/–12). Pt. 1 (right). Again, a potential to incorrect feedback tones is recorded in the anterior cingulate gyrus (G12) (⋄), as well as in other limbic sites including the posterior hippocampus (p-HC) (C26) (□) and the posterior parahippocampal gyrus (p-pHCg) (D24) (○). These sites all generate a positivity at ∼300 ms that resembles the simultaneous P300 recorded at the scalp (Pz) (△). The same sites showed little or no response to the input stimuli, except for the catch trials (shown only for the anterior cingulate gyrus) (G9) (⋄). Probe coordinates (actual followed by normalized): probe D (24/–45/11 and 24/–44/11), probe C (26/26/–39/–3 and 26/–38/–4) and probe G (9–12/36/2 and 9–12/36/2).

1
Present address: Nuclear Magnetic Resonance Center, Department of Radiology, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA, USA
2
Present address: INSERM E9926, Marseilles, France
3
Present address: Department of Psychology, University of Angers

We thank Natalie Hervé, Gerry Larson, Alain Lieury, Ksenija Marinkoviç, Ole Jensen, Terry Allard, Jeremy Jordin, Maureen Glessner, Jean-Marie Scarabin, John Klopp and Veronique Hédou for their contributions to this research. This work was supported by the Office of Naval Research, INSERM, USPHS (NS18741) and the HFSPO (RG0025/96).

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