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Describing the maturation of information processing in children is fundamental for developmental science. Although non-linear changes in reaction times have been well-documented, direct measurement of the development of the different processing components is lacking. In this study, electromyography was used to quantify the maturation of premotor and motor processes on a sample of 114 children (6-14 years-old) and 15 adults. Using a model-based approach, we show that the development of these two components is well-described by an exponential decrease in duration, with the decay rate being equal for the two components. These findings provide the first unbiased evidence in favour of the common developmental rate of nonmotor and motor processes by directly confronting rates of development of different processing components within the same task. This common developmental rate contrasts with the differential physical maturation of region-specific cerebral gray and white matter. Tentative paths of interpretation are proposed in the discussion., Competing Interests: The authors have declared that no competing interests exist.

Background: Deep brain stimulation of the subthalamic nucleus (STN DBS) is known to increase response speed and lower response accuracy in Parkinson's disease (PD) patients. It has been proposed that this speed-accuracy tradeoff is due to enhanced sensitivity of the motor system to sensory information. An alternative possibility is that this effect is due to weakened suppressive processes. The two alternative interpretations can be tested by analyzing the electromyographic activity (EMG) of the response agonists when the patients perform conflict reaction time tasks. In those tasks, fast subthreshold muscle impulses often occur in the agonist of the incorrect response. These impulses are partial errors that are suppressed before being behaviourally committed., Material and Methods: Here we analyzed the EMG of the response agonists recorded while sixteen PD patients performed a Simon task that elicits prepotent response tendencies so as to decipher (i) whether STN DBS affects the expression and/or suppression of subthreshold muscle impulses that are critical for action control and (ii) the interaction between dopaminergic treatment and STN DBS. The patients were tested On and Off STN DBS and On and Off dopaminergic medication in a full factorial design., Results: STN DBS not only impaired the proficiency to suppress subliminal action impulses (p = 0.01) but also favoured the muscular expression of fast incorrect impulses (p < 0.001). Dopaminergic treatment only affected the action impulses suppression (p = 0.02) and did not change the effect of STN DBS on impulsive action control., Conclusion: Contrary to a recent proposal, STN DBS impaired rather than improved action control by weakening erroneous impulse suppression, whether the patients were On or Off their usual medication. These findings are discussed in light of a recent proposal (Servant M, White C, Montagnini A, Burle B, 2015) that reconciles partial errors with accumulation-to-bound models of decision making. Our results suggest that medication specifically lowers the mechanical threshold while STN DBS lowers the mechanical threshold and to a lesser extent the EMG-threshold., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

Both in real life and experimental settings, increasing response speed typically leads to more error-prone actions. Processes underlying such a "speed-accuracy trade-off" (SAT) are usually assumed to be purely decisional: cautiousness would be determined only by the amount of sensory evidence required to select a response. The present data challenges this largely accepted view, by directly showing that motor processes are speeded up under time pressure. In a choice reaction time task where emphasis was put either on response speed or accuracy, motor processes were investigated through the analysis of muscular activity related to response execution. When response speed was emphasized, the time between electromyographic onset and behavioral response (motor time) was also speeded up (contributing to more than 20 % of the total effect on global reaction time). This speeded execution (likely due to a more efficient motor command) may also explain why participants are less able to interrupt incorrect response execution once started (Burle et al., Psychonomic Bulletin & Review, 21(4), 1003-1010, 2014), leading to more overt errors. Pointing to a speed-accuracy exchange within motor processes themselves, the present results call for a re-evaluation of widely accepted assumptions about SAT, and more generally, decision-making processes. They are discussed in the context of recent extensions of the drift diffusion model framework, questioning the strict separation between decisional and motor processes.

A current challenge for decision-making research is in extending models of simple decisions to more complex and ecological choice situations. Conflict tasks (e.g., Simon, Stroop, Eriksen flanker) have been the focus of much interest, because they provide a decision-making context representative of everyday life experiences. Modeling efforts have led to an elaborated drift diffusion model for conflict tasks (DMC), which implements a superimposition of automatic and controlled decision activations. The DMC has proven to capture the diversity of behavioral conflict effects across various task contexts. This study combined DMC predictions with EEG and EMG measurements to test a set of linking propositions that specify the relationship between theoretical decision-making mechanisms involved in the Simon task and brain activity. Our results are consistent with a representation of the superimposed decision variable in the primary motor cortices. The decision variable was also observed in the EMG activity of response agonist muscles. These findings provide new insight into the neurophysiology of human decision-making. In return, they provide support for the DMC model framework.

In a rich environment, with multiple action affordances, selective action inhibition is critical in preventing the execution of inappropriate responses. Here, we studied the origin and the dynamics of incorrect response inhibition and how it can be modulated by task demands. We used EEG in a conflict task where the probability of compatible and incompatible trials was varied. This allowed us to modulate the strength of the prepotent response, and hence to increase the risk of errors, while keeping the probability of the two responses equal. The correct response activation and execution was not affected by compatibility or by probability. In contrast, incorrect response inhibition in the primary motor cortex ipsilateral to the correct response was more pronounced on incompatible trials, especially in the condition where most of the trials were compatible, indicating a modulation of inhibitory strength within the course of the action. Two prefrontal activities, one medial and one lateral, were also observed before the response, and their potential links with the observed inhibitory pattern observed are discussed., (© 2016 The Authors. Psychophysiology published by Wiley Periodicals, Inc. on behalf of Society for Psychophysiological Research.)

Among the different brain imaging techniques, electroencephalography (EEG) is classically considered as having an excellent temporal resolution, but a poor spatial one. Here, we argue that the actual temporal resolution of conventional (scalp potentials) EEG is overestimated, and that volume conduction, the main cause of the poor spatial resolution of EEG, also distorts the recovered time course of the underlying sources at scalp level, and hence degrades the actual temporal resolution of EEG. While Current Source Density (CSD) estimates, through the Surface Laplacian (SL) computation, are well known to dramatically reduce volume conduction effects and hence improve EEG spatial resolution, its positive impact on EEG temporal resolution is much less recognized. In two simulation studies, we first show how volume conduction and reference electrodes distort the scalp potential time course, and how SL transform provides a much better spatio-temporal description. We then exemplify similar effects on two empirical datasets. We show how the time courses of the scalp potentials mis-estimate the latencies of the relevant brain events and that CSD provides a much richer, and much more accurate, view of the spatio-temporal dynamics of brain activity., (Copyright © 2015. Published by Elsevier B.V.)

Most decisions that we make build upon multiple streams of sensory evidence and control mechanisms are needed to filter out irrelevant information. Sequential sampling models of perceptual decision making have recently been enriched by attentional mechanisms that weight sensory evidence in a dynamic and goal-directed way. However, the framework retains the longstanding hypothesis that motor activity is engaged only once a decision threshold is reached. To probe latent assumptions of these models, neurophysiological indices are needed. Therefore, we collected behavioral and EMG data in the flanker task, a standard paradigm to investigate decisions about relevance. Although the models captured response time distributions and accuracy data, EMG analyses of response agonist muscles challenged the assumption of independence between decision and motor processes. Those analyses revealed covert incorrect EMG activity ("partial error") in a fraction of trials in which the correct response was finally given, providing intermediate states of evidence accumulation and response activation at the single-trial level. We extended the models by allowing motor activity to occur before a commitment to a choice and demonstrated that the proposed framework captured the rate, latency, and EMG surface of partial errors, along with the speed of the correction process. In return, EMG data provided strong constraints to discriminate between competing models that made similar behavioral predictions. Our study opens new theoretical and methodological avenues for understanding the links among decision making, cognitive control, and motor execution in humans., Significance Statement: Sequential sampling models of perceptual decision making assume that sensory information is accumulated until a criterion quantity of evidence is obtained, from where the decision terminates in a choice and motor activity is engaged. The very existence of covert incorrect EMG activity ("partial error") during the evidence accumulation process challenges this longstanding assumption. In the present work, we use partial errors to better constrain sequential sampling models at the single-trial level., (Copyright © 2015 the authors 0270-6474/15/3510371-15$15.00/0.)

Rationale: Impulsive actions entail (1) capture of the motor system by an action impulse, which is an urge to act and (2) failed suppression of that impulse in order to prevent a response error. Several studies indicate that dopaminergic treatment can induce action impulsivity in patients diagnosed with Parkinson's disease (PD). Whether this effect is due to increased impulse expression or to decreased impulse suppression remains to be deciphered., Method: We used a novel approach based on electromyographic (EMG) analyses to decipher the effects of the patient's usual dopaminergic therapy on the expression and suppression of subliminal erroneous impulses. To this end, we used a within-subject design and took advantage of the Simon task, that elicits prepotent response tendencies. The patients (N = 15) performed the task on their usual dopaminergic medication and after complete medication withdrawal (for at least 12 h)., Results: The correction rate that measures the ability to suppress subthreshold impulsive muscle activity was lower when the patients were on medication as compared to their off medication state (p < 0.05). The incorrect activation rate that measures the capture of the motor system by action impulses was unaffected by medication., Conclusions: Dopa therapy affected action impulsivity. Although medication did not influence the incidence of fast action impulses, it significantly reduced patients' ability to abort and suppress muscle activation related to the incorrect response alternative.

To err is human. However, an inappropriate urge does not always result in error. Impulsive errors thus entail both a motor system capture by an urge to act and a failed inhibition of that impulse. Here we show that neuromodulatory electrical stimulation of the supplementary motor complex in healthy humans leaves action urges unchanged but prevents them from turning into overt errors. Subjects performed a choice reaction-time task known to trigger impulsive responses, leading to fast errors that can be revealed by analyzing accuracy as a function of poststimulus time. Yet, such fast errors are only the tip of the iceberg: electromyography (EMG) revealed fast subthreshold muscle activation in the incorrect response hand in an even larger proportion of overtly correct trials, revealing covert response impulses not discernible in overt behavior. Analyzing both overt and covert response tendencies enables to gauge the ability to prevent these incorrect impulses from turning into overt action errors. Hyperpolarizing the supplementary motor complex using transcranial direct current stimulation (tDCS) preserves action impulses but prevents their behavioral expression. This new combination of detailed behavioral, EMG, and tDCS techniques clarifies the neurophysiology of impulse control, and may point to avenues for improving impulse control deficits in various neurologic and psychiatric disorders., (Copyright © 2015 the authors 0270-6474/15/333010-06$15.00/0.)

To describe the mental architecture between stimulus and response, cognitive models often divide the stimulus-response (SR) interval into stages or modules. Predictions derived from such models are typically tested by focusing on the moment of response emission, through the analysis of response time (RT) distributions. To go beyond the single response event, we recently proposed a method to fractionate verbal RTs into two physiologically defined intervals that are assumed to reflect different processing stages. The analysis of the durations of these intervals can be used to study the interaction between cognitive and motor processing during speech production. Our method is inspired by studies on decision making that used manual responses, in which RTs were fractionated into a premotor time (PMT), assumed to reflect cognitive processing, and a motor time (MT), assumed to reflect motor processing. In these studies, surface EMG activity was recorded from participants' response fingers. EMG onsets, reflecting the initiation of a motor response, were used as the point of fractionation. We adapted this method to speech-production research by measuring verbal responses in combination with EMG activity from facial muscles involved in articulation. However, in contrast to button-press tasks, the complex task of producing speech often resulted in multiple EMG bursts within the SR interval. This observation forced us to decide how to operationalize the point of fractionation: as the first EMG burst after stimulus onset (the stimulus-locked approach), or as the EMG burst that is coupled to the vocal response (the response-locked approach). The point of fractionation has direct consequences on how much of the overall task effect is captured by either interval. Therefore, the purpose of the current paper was to compare both onset-detection procedures in order to make an informed decision about which of the two is preferable. We concluded in favor or the response-locked approach.

When an on-board system detects a drift of a vehicle to the left or to the right, in what way should the information be delivered to the driver? Car manufacturers have so far neglected relevant results from Experimental Psychology and Cognitive Neuroscience. Here we show that this situation possibly led to the sub-optimal design of a lane departure warning system (AFIL, PSA Peugeot Citroën) implemented in commercially available automobile vehicles. Twenty participants performed a two-choice reaction time task in which they were to respond by clockwise or counter-clockwise wheel-rotations to tactile stimulations of their left or right wrist. They performed poorer when responding counter-clockwise to the right vibration and clockwise to the left vibration (incompatible mapping) than when responding according to the reverse (compatible) mapping. This suggests that AFIL implements the worse (incompatible) mapping for the operators. This effect depended on initial practice with the interface. The present research illustrates how basic approaches in Cognitive Science may benefit to Human Factors Engineering and ultimately improve man-machine interfaces and show how initial learning can affect interference effects.

In conflict tasks, the irrelevant stimulus attribute needs to be suppressed for the correct response to be produced. In the Simon task, earlier researchers have proposed that this suppression is the reason that, after an initial increase, the interference effect decreases for longer RTs, as reflected by late, negative-going delta plots. This view has been challenged by observations of positive-going delta plots, even for long RTs, in other conflict tasks, despite a similar necessity for suppression. For late negative-going delta plots to be interpreted as reflecting suppression, a necessary, although maybe not sufficient, condition is that similar patterns should be observed for other conflict tasks. We reasoned that a similar suppression could be present, but hidden, in the Eriksen flanker task. By recording and analyzing electromyograms of the muscles involved in response execution, we could compute delta plots separately for trials that elicited a subthreshold incorrect response activation (partial error). Late negative-going delta plots were observable on partial-error trials, although they were weaker than for the Simon task, reducing the impact of this inversion on the overall distribution. We further showed that this pattern is modulated by time pressure. Those results indicate that mechanisms leading to negative-going delta plots, similar to those observed in the Simon task, are also at play in the Eriksen task. The link between negative-going delta plots and executive online control is discussed.

Formal models of decision-making have traditionally focused on simple, two-choice perceptual decisions. To date, one of the most influential account of this process is Ratcliff's drift diffusion model (DDM). However, the extension of the model to more complex decisions is not straightforward. In particular, conflicting situations, such as the Eriksen, Stroop, or Simon tasks, require control mechanisms that shield the cognitive system against distracting information. We adopted a novel strategy to constrain response time (RT) models by concurrently investigating two well-known empirical laws in conflict tasks, both at experimental and modeling levels. The two laws, predicted by the DDM, describe the relationship between mean RT and (i) target intensity (Piéron's law), (ii) standard deviation of RT (Wagenmakers-Brown's law). Pioneering work has shown that Piéron's law holds in the Stroop task, and has highlighted an additive relationship between target intensity and compatibility. We found similar results in both Eriksen and Simon tasks. Compatibility also violated Wagenmakers-Brown's law in a very similar and particular fashion in the two tasks, suggesting a common model framework. To investigate the nature of this commonality, predictions of two recent extensions of the DDM that incorporate selective attention mechanisms were simulated and compared to the experimental results. Both models predict Piéron's law and the violation of Wagenmakers-Brown's law by compatibility. Fits of the models to the RT distributions and accuracy data allowed us to further reveal their relative strengths and deficiencies. Combining experimental and computational results, this study sets the groundwork for a unified model of decision-making in conflicting environments., (Copyright © 2014 The Authors. Published by Elsevier Inc. All rights reserved.)

The cortical regions involved in the different stages of speech production are relatively well-established, but their spatio-temporal dynamics remain poorly understood. In particular, the available studies have characterized neural events with respect to the onset of the stimulus triggering a verbal response. The core aspect of language production, however, is not perception but action. In this context, the most relevant question may not be how long after a stimulus brain events happen, but rather how long before the production act do they occur. We investigated speech production-related brain activity time-locked to vocal onset, in addition to the common stimulus-locked approach. We report the detailed temporal interplay between medial and left frontal activities occurring shortly before vocal onset. We interpret those as reflections of, respectively, word selection and word production processes. This medial-lateral organization is in line with that described in non-linguistic action control, suggesting that similar processes are at play in word production and non-linguistic action production. This novel view of the brain dynamics underlying word production provides a useful background for future investigations of the spatio-temporal brain dynamics that lead to the production of verbal responses.

Since the 19th century, it has been known that response latencies are longer for naming pictures than for reading words aloud. While several interpretations have been proposed, a common general assumption is that this difference stems from cognitive word-selection processes and not from articulatory processes. Here we show that, contrary to this widely accepted view, articulatory processes are also affected by the task performed. To demonstrate this, we used a procedure that to our knowledge had never been used in research on language processing: response-latency fractionating. Along with vocal onsets, we recorded the electromyographic (EMG) activity of facial muscles while participants named pictures or read words aloud. On the basis of these measures, we were able to fractionate the verbal response latencies into two types of time intervals: premotor times (from stimulus presentation to EMG onset), mostly reflecting cognitive processes, and motor times (from EMG onset to vocal onset), related to motor execution processes. We showed that premotor and motor times are both longer in picture naming than in reading, although than in reading, although articulation is already initiated in the latter measure. Future studies based on this new approach should bring valuable clues for a better understanding of the relation between the cognitive and motor processes involved in speech production.

We investigated the influence of temporal preparation on information processing. Single-pulse transcranial magnetic stimulation (TMS) of the primary motor cortex was delivered during a between-hand choice task. The time interval between the warning and the imperative stimulus varied across blocks of trials was either optimal (500 ms) or nonoptimal (2500 ms) for participants' performance. Silent period duration was shorter prior to the first evidence of response selection for the optimal condition. Amplitude of the motor evoked potential specific to the responding hand increased earlier for the optimal condition. These results revealed an early release of cortical inhibition and a faster integration of the response selection-related inputs to the corticospinal pathway when temporal preparation is better. Temporal preparation may induce cortical activation prior to response selection that speeds up the implementation of the selected response., (Copyright © 2011 Society for Psychophysiological Research.)

While there is general agreement that in Parkinson's disease (PD), striatal dopamine (DA) depletion causes motor deficits, the origin of the associated cognitive impairments remains a matter of debate. The present study aimed to decipher the influence of a partial 6-hydroxydopamine (6-OHDA) lesion of striatal DA nerve terminals in rats performing a reaction time task previously used to assess cognitive deficits in PD patients. The effects of two behavioral manipulations-foreperiod duration and stimulus-response congruence-known to affect motor processes and executive control, respectively, were studied over 8 weeks postsurgery in control and lesion animals. Two weeks after surgery, the lesion abolished the effect of foreperiod, confirming the direct involvement of striatal DA in motor processes, but failed to alter the effect of congruence. During the following weeks, the effect of foreperiod was reinstated, indicating a recovery of lesion-induced motor symptoms. This recovery was accompanied by a progressive increase of the congruence effect, signaling an executive control deficit in lesion animals. This result provides the first evidence that 6-OHDA lesioned rats exhibit the same cognitive impairment as PD patients in this task. The deficit, however, built up progressively after the lesion and may result from adaptations mitigating lesion-induced motor deficits.

The concept of "monitoring" refers to our ability to control our actions on-line. Monitoring involved in speech production is often described in psycholinguistic models as an inherent part of the language system. We probed the specificity of speech monitoring in two psycholinguistic experiments where electroencephalographic activities were recorded. Our focus was on a component previously reported in nonlinguistic manual tasks and interpreted as a marker of monitoring processes. The error negativity (Ne, or error-related negativity), thought to originate in medial frontal areas, peaks shortly after erroneous responses. A component of seemingly comparable properties has been reported, after errors, in tasks requiring access to linguistic knowledge (e.g., speech production), compatible with a generic error-detection process. However, in contrast to its original name, advanced processing methods later revealed that this component is also present after correct responses in visuomotor tasks. Here, we reported the observation of the same negativity after correct responses across output modalities (manual and vocal responses). This indicates that, in language production too, the Ne reflects on-line response monitoring rather than error detection specifically. Furthermore, the temporal properties of the Ne suggest that this monitoring mechanism is engaged before any auditory feedback. The convergence of our findings with those obtained with nonlinguistic tasks suggests that at least part of the monitoring involved in speech production is subtended by a general-purpose mechanism.

An essential facet of adaptive and versatile behavior is the ability to prioritize actions in response to dynamically changing circumstances. The field of potential actions afforded by a situation is shaped by many factors, such as environmental demands, past experiences, and prepotent tendencies. Selection among action affordances can be driven by deliberate, intentional processes as a product of goal-directed behavior and by extraneous stimulus-action associations as established inherently or through learning. We first review the neurocognitive mechanisms putatively linked to these intention-driven and association-driven routes of action selection. Next, we review the neurocognitive mechanisms engaged to inhibit action affordances that are no longer relevant or that interfere with goal-directed action selection. Optimal action control is viewed as a dynamic interplay between selection and suppression mechanisms, which is achieved by an elaborate circuitry of interconnected cortical regions (most prominently the pre-supplementary motor area and the right inferior frontal cortex) and basal ganglia structures (most prominently the dorsal striatum and the subthalamic nucleus). WIREs Cogni Sci 2011 2 174-192 DOI: 10.1002/wcs.99 For further resources related to this article, please visit the WIREs website., (Copyright © 2010 John Wiley & Sons, Ltd.)

To head rather than heed to temptations is easier said than done. Since tempting actions are often contextually inappropriate, selective suppression is invoked to inhibit such actions. Thus far, laboratory tasks have not been very successful in highlighting these processes. We suggest that this is for three reasons. First, it is important to dissociate between an early susceptibility to making stimulus-driven impulsive but erroneous actions, and the subsequent selective suppression of these impulses that facilitates the selection of the correct action. Second, studies have focused on mean or median reaction times (RT), which conceals the temporal dynamics of action control. Third, studies have focused on group means, while considering individual differences as a source of error variance. Here, we present an overview of recent behavioral and imaging studies that overcame these limitations by analyzing RT distributions. As will become clear, this approach has revealed variations in inhibitory control over impulsive actions as a function of task instructions, conflict probability, and between-trial adjustments (following conflict or following an error trial) that are hidden if mean RTs are analyzed. Next, we discuss a selection of behavioral as well as imaging studies to illustrate that individual differences are meaningful and help understand selective suppression during action selection within samples of young and healthy individuals, but also within clinical samples of patients diagnosed with attention deficit/hyperactivity disorder or Parkinson's disease.

Falkenstein et al. (1991) first described a negative wave occurring just after an erroneous response in choice Reaction time tasks ("Error Negativity"-Ne or "Error Related Negativity"-ERN). Thanks to Laplacian transform of the data, Vidal et al. (2000, 2003a) described a wave on correct trials with similar topography and latency, although of smaller amplitude compared to the errors. A critical question is whether the Ne observed on errors and the negativity reported on correct trials reflect the same (modulated) activity, or whether they reflect completely different mechanisms. These two alternative possibilities were tested thanks to Independent Component Analysis (ICA) and source localization. ICA results showed that the waves recorded on errors and correct trials can be accounted for by the same independent component, corresponding to a dipolar source located within the Rostral Cingulate Zone. Source localization on the raw data also confirmed a common generator for correct and error trials. These data suggest that the waves on errors and correct trials reflect the same brain activity, whose amplitude varies as a function of the correctness of the response. The implications of this result for cognitive control are discussed., (Copyright (c) 2010 Elsevier Inc. All rights reserved.)

The ability to stop ongoing motor responses in a split-second is a vital element of human cognitive control and flexibility that relies in large part on prefrontal cortex. We used the stop-signal paradigm to elucidate the engagement of primary motor cortex (M1) in inhibiting an ongoing voluntary motor response. The stop-signal paradigm taps the ability to flexibly countermand ongoing voluntary behavior upon presentation of a stop signal. We applied single-pulse TMS to M1 at several intervals following the stop signal to track the time course of excitability of the motor system related to generating and stopping a manual response. Electromyography recorded from the flexor pollicis brevis allowed quantification of the excitability of the corticospinal tract and the involvement of intracortical GABA(B)ergic circuits within M1, indexed respectively by the amplitude of the motor-evoked potential and the duration of the late part of the cortical silent period (SP). The results extend our knowledge of the neural basis of inhibitory control in three ways. First, the results revealed a dynamic interplay between response activation and stopping processes at M1 level during stop-signal inhibition of an ongoing response. Second, increased excitability of inhibitory interneurons that drives SP prolongation was evident as early as 134 msec following the instruction to stop. Third, this pattern was followed by a stop-related reduction of corticospinal excitability implemented around 180 after the stop signal. These findings point to the recruitment of GABA(B)ergic intracortical inhibitory circuits within M1 in stop-signal inhibition and support the notion of stopping as an active act of control.

The parieto-frontal network plays a crucial role in the transformations that convert visual information into motor commands for hand reaching movements. Here we use electroencephalography to determine whether the planning of reaching movements to visual and somatosensory targets involves a similar spatio-temporal pattern of neural activity. Subjects performed reaching movements toward spatial locations defined either by visual (light-emitting diode) or somatosensory (vibration of a fingertip of the contralateral hand) stimuli. To identify the activations associated with sensorimotor transformations, we subtracted the event-related potentials recorded in a "static" task (the stimuli were presented but no movement was initiated) from those recorded in a "reach" task (a reach had to be initiated toward the spatial location of the stimuli). In the visual condition, reach-related activities were observed over parietal, premotor and sensorimotor areas contralateral to the reaching hand. Activation was first observed over parietal areas 140 ms after stimulus onset and progressed to frontal areas. The proprioceptive condition recruited a similar set of structures as for visual targets. However, the temporal pattern of activity within these cortical areas differed greatly. Activity was sustained over premotor and sensorimotor areas throughout the reaction time interval, occurring simultaneously with the parietal activation. These results suggest that a common cortical network serves to transform visual and somatosensory signals into motor commands, but that the interactions between the structures of this network differ. This raises the possibility that different coordinate frames are used to encode the motor error for the two target modalities.

Upon exposure to novel visuomotor relationships, the information carried by visual and proprioceptive signals becomes discrepant, often disrupting motor execution. It has been shown that degradation of the proprioceptive sense (arising either from disease or experimental manipulation) enhances performance when drawing with mirror-reversed vision. Given that the central nervous system can exert a dynamic control over the transmission of afferent signals, reducing proprioceptive inflow to cortical areas could be part of the normal adaptive mechanisms deployed in healthy humans upon exposure to novel visuomotor environments. Here we address this issue by probing the transmission of somatosensory afferents throughout the course of adaptation to a visuomotor conflict, by recording median nerve somatosensory evoked potentials. We show that early exposure to tracing with mirror-reversed vision is accompanied by substantial proprioceptive suppression occurring in the primary somatosensory cortex (S1). This proprioceptive gating is gradually alleviated as performance increases with adaptation, returning to baseline levels. Peripheral and spinal evoked potentials were not modulated throughout, suggesting that the gating acted to reduce cortico-cortico excitability directly within S1. These modulations provide neurophysiological evidence for flexibility in sensory integration during visuomotor adaptation, which may functionally serve to reduce the sensory conflict until the visuo-proprioceptive mapping is updated.

Behavioral estimates of time discrimination threshold on animals might be contaminated by the conditioning procedure used and by attentional effects. To avoid such side effects, we measured time discrimination by recording the rat electroencephalographic response to small temporal variations. Freely moving rats were presented with repetitive sounds, some of them being occasionally shorter than the standard, to produce a Mismatch Negativity (MMN) which is known to primarily involve preattentive processes. The smallest difference eliciting a MMN located the discrimination threshold between 16% and 33% of the standard, without attentional confound. Being observed in several species, MMN can be used to decipher both the phylogenetic and ontogenetic evolution of time discrimination, without attentional confound.

Our ability to detect and correct errors is essential for our adaptive behavior. The conflict-loop theory states that the anterior cingulate cortex (ACC) plays a key role in detecting the need to increase control through conflict monitoring. Such monitoring is assumed to manifest itself in an electroencephalographic (EEG) component, the "error negativity" (Ne or "error-related negativity" [ERN]). We have directly tested the hypothesis that the ACC monitors conflict through simulation and experimental studies. Both the simulated and EEG traces were sorted, on a trial-by-trial basis, as a function of the degree of conflict, measured as the temporal overlap between incorrect and correct response activations. The simulations clearly show that conflict increases as temporal overlap between response activation increases, whereas the experimental results demonstrate that the amplitude of the Ne decreases as temporal overlap increases, suggesting that the ACC does not monitor conflict. At a functional level, the results show that the duration of the Ne depends on the time needed to correct (partial) errors, revealing an "on-line" modulation of control on a very short time scale.

The objective was to test whether motor preparation can modulate the efficiency of the cortical motor command. The electroencephalogram (EEG) was recorded from electrodes located over the primary sensorimotor cortices during the performance of a between-hand choice reaction time task in which foreperiod duration (the interval between the warning and the imperative signals, 800 vs. 2800 ms) was varied across blocks of trials. In order to increase the spatial resolution of the EEG traces, surface Laplacian was estimated. The amplitude of the negative wave developing over the hemisphere contralateral to the response was smaller for the short foreperiod associated with the best performance level. These results indicate that the activation of the primary sensorimotor cortex involved in the response is less pronounced for the short foreperiod, suggesting that temporal advance information increases the efficiency of the cortical motor command.

The aim of the current study was to assess the effects of physical exercise on simple reaction time performance. Participants performed a simple reaction time task twice, one time during physical exercise and another time without exercise. Electromyographic signals were recorded from the thumb of the responding hand to fraction reaction time in pre-motor and motor time. The results showed that exercise shortened motor time but failed to affect pre-motor time. This pattern of findings is consistent with previous studies examining the effects of physical exercise on choice reaction time.

Choice reaction time (RT) is shorter when participants perform a choice task at the same time as a sub-maximal exercise than when they are at rest. The purpose of the present study was to determine whether such an exercise affects response execution or whether it alters processes located upstream from the neuro-muscular level. To this end, the electromyographic (EMG) activity of the response agonists was analysed in a between-hand choice RT task performed either concurrently with a pedalling task or at rest. Visual stimulus intensity was also manipulated so as to determine whether exercise further affects early sensory processes. Results shows that exercise affected the time interval elapsing from the onset of the contraction of the response agonists to the mechanical response, thereby indicating that this variable modifies the peripheral motor processes involved in response execution. EMG signal analyses further revealed that the cortico-spinal command is more efficient during exercise than at rest. In addition, exercise was shown to interact with visual stimulus intensity on the time between stimulus and voluntary EMG onset and to increase the critical flicker fusion frequency threshold, thereby indicating that exercise modifies the peripheral sensory processes involved in early sensory operations. The decomposition of RT, with respect to the EMG activity of response agonists, sheds light on the processes affected by exercise and suggests that exercise affects both sensory processes and late motor processes.

Although it is widely accepted that control mechanisms are necessary for human behavior to be adapted, very little is known about how such mechanisms are recruited. A suggestion to fill the gap was put forward by M. M. Botvinick, T. S. Braver, C. S. Carter, D. M. Barch, and J. D. Cohen (2001), who proposed the conflict-loop theory. This theory has been successful in accounting for the reduction of compatibility effects after an incompatible trial: The level of conflict being, on average, higher during an incompatible trial, more control occurs after such a trial. The authors have tested this prediction by sorting the trials on the basis of amount of conflict (quantified by the electromyographic activity) they presented. A reduction of the compatibility effect was observed after incompatible trials, but it was independent of the level of conflict on previous trials, suggesting that the conflict does not trigger changes in executive control. Consequences for the conflict monitoring model are discussed.

In reaction time (RT) tasks, event-related potentials (ERPs) reveal a response-locked negative wave when subjects commit errors. This wave, termed "error negativity" (Ne) or "error-related negativity" (ERN), is thought to index response-monitoring processes. With conventional monopolar recordings, this negativity is hardly seen on correct responses, likely overlapped by a large positive wave. Indeed, after Laplacian transformation (a spatial high-pass filter), a small Ne-like wave is unmasked. Recently, it has been shown that the positivity on monopolar recordings was larger for correct responses preceding an error than for correct responses preceding a correct trial. After Laplacian transformation, it appears that this effect is due, at least in part, to a decrease of the Ne-like wave on correct responses preceding an error. This result indicates that, as the Ne on errors, the Ne-like wave on correct responses is sensitive to performance and hence is likely related to response-monitoring processes.

The nogo potentials (N2/P3) were studied in a precuing auditory reaction time task in human subjects who had to either perform a button-press response (Press condition) or imagine they were performing it (Imagine condition). In the full precue condition (the subjects knew in advance which response they had to perform/imagine), in 25% of the trials, a nogo signal instructed the subject not to perform or not to imagine the prepared action. Clear N2/P3 components were obtained on nogo trials on the Press trials, but also on the Imagine ones: the N2 was of similar amplitude in both conditions, whereas the P3 was of smaller amplitude in the Imagine condition. The presence of nogo potential in motor imagery is discussed in terms of the functional significance of the N2/P3 complex.

Manual responses to lateralized stimuli are faster for spatially congruent stimulus-response associations than for incongruent associations, even if the stimulus location is irrelevant. This effect, however, decreases as reaction time increases. Recent data suggest that such a decrease reflects online, within-trial executive control. The present study was aimed at testing this hypothesis by analyzing the electromyographic activity of muscles involved in response execution. We focused on the particular trials in which an activation of the muscle involved to the incorrect response preceded the execution of the correct response. A sequential effect analysis, along with an analysis of the reaction time distributions, revealed that after such dual-activation trials, executive control was reinforced. In addition, a distribution analysis of the reaction times associated with such trials compared to the trials without incorrect activation, revealed online, within-trial changes in executive control. Arguments against a late motor locus of the effect of the irrelevant stimulus location are also provided. These results are discussed in terms of current models of cognitive control.

We present evidence that advance information reducing the number of stimulus-response alternatives in a choice reaction time (RT) task can shorten the very latest motoric stages of RT. Effects of such advance information on late stages of RT have been demonstrated recently by Osman, Moore, and Ulrich (Acta Psychol. 90 (1995) 111), Leuthold, Sommer, and Ulrich (J. Exp. Psychol: Gen. 125 (1996) 307), Müller-Gethmann, Rinkenauer, Stahl, and Ulrich (Psychophysiology 37 (2000) 507). These studies found that advance information shortens the portion of the RT interval following onset of a movement-related brain potential (lateralized readiness potential). Osman et al. and Müller-Gethmann et al. also examined the portion of the RT interval following the start of electromyographic (EMG) activity and found no effect of advance information. Based on Osman et al.'s null result, Leuthold et al. speculated that advance information may shorten only the RT stages preceding EMG activity. This conclusion, however, is questionable because of limitations in the EMG measures employed by both Osman et al. and Müller-Gethmann et al. We have reanalyzed the results of a previously reported experiment (Acta Psychol. 101 (1999) 243) to show that advance information can in fact affect the rate of recruitment of motor units in the prime mover of the responding limb.

In the field of sensorimotor activities, progresses achieved over the last fifty years have been largely driven by the Reaction Time (RT) paradigm. Information processing models are set in the context of a global breakdown of sensorimotor activities in multiple concatenated stages, each aggregated in many fundamental operations that are functionally linked. If there is a consensus today about this breakdown, the way stages organize themselves in time however is still much debated. According to one hypothesis, there is no temporal overlap between each stages: the process occurs sequentially. According to another theory, the stages overlap over in time: the process occurs in a parallel manner. A behavioral analysis does not allow to determine between these two hypothesis because the RT represents the final product of the whole sensorimotor pathway, while the temporal organization of the processing of information depends on the nature of the transfer between individual stages. An all-or-nothing information transfer, also called discrete, leads to a sequential organization, while a progressive or continuous transfer brings about a parallel organization. Moreover, contrary to a preconceived notion, data obtained from classical neurophysiology are compatible with both a sequential organization and a parallel organization. Particularly, the great number of connections between the different elements of the nervous system has often seemed difficult to conciliate with a sequential organization. In fact, this argument is inadmissible because it stems from confusion between a temporal organization and an anatomical organization of the processing of information. More generally, our knowledge of the functional anatomy of sensorimotor activities imposes but few constraints on the temporal organization patterns of the processing of information. The lack of interest for the neurophysiological argument seems essentially due to the fact that theses arguments rest on research which is not aimed at the temporal organization of the sensorimotor information processing. Recently, approaches that integrate concepts and methods used in experimental psychology and neurosciences have contributed to putting in perspective the organization of information processing. Electromyography, EEG, reflexology and neuronal recording techniques have been used in the context of two inference logics. The first logic, that we call "factual", is based on the study of functional relations between RT and certain neuronal events. The second logic, that we call "chronometric", is based on the study of the relationships between RT and intervals resulting from the breakdown of the RT in relation to certain neuronal events. Generally speaking, most studies suggest that in tasks where the stimulus is composed of numerous attributes, information processing operates in parallel. On the other hand, when the stimulus is made up of a single attribute, information processing could be operating in a sequential manner. One weakness of this electrophysiological approach is that it has so far only examined relationships between physiological indicators and means RT. We propose here to offset these weaknesses by examining functional relationships between RT distribution variances and certain neuronal events linked to information processing.