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The neural basis of error detection: conflict monitoring and the error-related negativity
- Psychological Review
, 2004
"... According to a recent theory, anterior cingulate cortex is sensitive to response conflict, the coactivation of mutually incompatible responses. The present research develops this theory to provide a new account of the error-related negativity (ERN), a scalp potential observed following errors. Conne ..."
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Cited by 35 (7 self)
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According to a recent theory, anterior cingulate cortex is sensitive to response conflict, the coactivation of mutually incompatible responses. The present research develops this theory to provide a new account of the error-related negativity (ERN), a scalp potential observed following errors. Connectionist simulations of response conflict in an attentional task demonstrated that the ERN—its timing and sensitivity to task parameters—can be explained in terms of the conflict theory. A new experiment confirmed predictions of this theory regarding the ERN and a second scalp potential, the N2, that is proposed to reflect conflict monitoring on correct response trials. Further analysis of the simulation data indicated that errors can be detected reliably on the basis of post-error conflict. It is concluded that the ERN can be explained in terms of response conflict and that monitoring for conflict may provide a simple mechanism for detecting errors. Errors are an important source of information in the regulation of cognitive processes. The mechanism by which people detect and correct their errors has been the object of study for many years, but research interest has increased in recent years following the discovery of neural correlates of performance monitoring. In particular,
The neural correlates and functional integration of cognitive control in a Stroop task
- NeuroImage
, 2005
"... It is well known that performance on a given trial of a cognitive task is affected by the nature of previous trials. For example, conflict effects on interference tasks, such as the Stroop task, are reduced subsequent to high-conflict trials relative to low-conflict trials. This interaction effect b ..."
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Cited by 6 (1 self)
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It is well known that performance on a given trial of a cognitive task is affected by the nature of previous trials. For example, conflict effects on interference tasks, such as the Stroop task, are reduced subsequent to high-conflict trials relative to low-conflict trials. This interaction effect between previous and current trial types is called bconflict adaptationQ and thought to be due to processing adjustments in cognitive control. The current study aimed to identify the neural substrates of cognitive control during conflict adaptation by isolating neural correlates of reduced conflict from those of increased cognitive control. We expected cognitive control to be implemented by prefrontal cortex through context-specific modulation of posterior regions involved in sensory and motor aspects of task performance. We collected event-related fMRI data on a color-word naming Stroop task and found distinct fronto-parietal networks of current trial conflict detection and conflict adaptation through cognitive control. Conflict adaptation was associated with increased activity in left middle frontal gyrus (GFm) and superior frontal gyrus (GFs), consistent with increased cognitive control, and with decreased activity in bilateral prefrontal and parietal cortices, consistent with reduced response conflict. Psychophysiological interaction analysis (PPI) revealed that cognitive control activation in GFs and GFm was accompanied by increased functional integration with bilateral inferior frontal, right temporal and parietal areas, and the anterior cerebellum. These data suggest that cognitive control is implemented by medial and lateral prefrontal cortices that bias processes in regions that have been implicated in high-level perceptual and motor processes.
Anterior cingulate cortex, selection for action, and error processing
- In M. Posner (Ed.), Cognitive neuroscience of attention
, 2004
"... The concepts of “attention to action ” (Norman & Shallice, 1986) and “selection for action ” (Allport, 1987) refer to how particular cognitive intentions and sensory inputs are selected and coupled with the effector ..."
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Cited by 6 (2 self)
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The concepts of “attention to action ” (Norman & Shallice, 1986) and “selection for action ” (Allport, 1987) refer to how particular cognitive intentions and sensory inputs are selected and coupled with the effector
Modulation of the semantic system by word imageability
, 2005
"... A prevailing neurobiological theory of semantic memory proposes that part of our knowledge about concrete, highly imageable concepts is stored in the form of sensory–motor representations. While this theory predicts differential activation of the semantic system by concrete and abstract words, previ ..."
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Cited by 3 (0 self)
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A prevailing neurobiological theory of semantic memory proposes that part of our knowledge about concrete, highly imageable concepts is stored in the form of sensory–motor representations. While this theory predicts differential activation of the semantic system by concrete and abstract words, previous functional imaging studies employing this contrast have provided relatively little supporting evidence. We acquired event-related functional magnetic resonance imaging (fMRI) data while participants performed a semantic similarity judgment task on a large number of concrete and abstract noun triads. Task difficulty was manipulated by varying the degree to which the words in the triad were similar in meaning. Concrete nouns, relative to abstract nouns, produced greater activation in a bilateral network of multimodal and heteromodal association areas, including ventral and medial temporal, posterior–inferior parietal, dorsal prefrontal, and posterior cingulate cortex. In contrast, abstract nouns produced greater activation almost
Correspondence should be addressed to:
"... We used fMRI to study the brain processes involved in the dynamic control of behaviour. The Sustained Attention to Response Task (SART), which allows unpredictable and predictable No-go events to be contrasted, was imaged using a mixed (block and event-related) fMRI design to examine tonic and phasi ..."
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We used fMRI to study the brain processes involved in the dynamic control of behaviour. The Sustained Attention to Response Task (SART), which allows unpredictable and predictable No-go events to be contrasted, was imaged using a mixed (block and event-related) fMRI design to examine tonic and phasic processes involved in response inhibition, error detection, conflict monitoring and sustained attention. A network of regions, including right ventral prefrontal cortex (PFC), left dorsolateral PFC and right inferior parietal cortex, was activated for successful unpredictable inhibitions, while rostral anterior cingulate was implicated in error processing and the pre-SMA in conflict monitoring. Furthermore, the pattern of correlations between left dorsolateral PFC, implicated in task-set maintenance, and the pre-SMA were indicative of a tight coupling between prefrontally mediated control and conflict levels monitored more posteriorly. The results reveal that the executive control of behaviour can be separated into distinct functions performed by discrete cortical regions. 2 The control over routine, everyday behaviour involves a number of complex executive
IS COMPREHENSION NECESSARY FOR ERROR DETECTION? A CONFLICT-BASED ACCOUNT OF MONITORING IN SPEECH PRODUCTION
, 2011
"... Although speech is error-prone, verbal communication is successful because speakers can detect (and correct) their errors. The standard theory of speech-error detection, the perceptual-loop account, posits that the comprehension system monitors production output for errors. Such a comprehension-base ..."
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Although speech is error-prone, verbal communication is successful because speakers can detect (and correct) their errors. The standard theory of speech-error detection, the perceptual-loop account, posits that the comprehension system monitors production output for errors. Such a comprehension-based monitor, however, cannot explain the double dissociation between comprehension and error-detection ability observed in the aphasic patients. We propose a new theory of speech-error detection which is, instead, based on the production process itself. The theory borrows from studies of forced-choiceresponse tasks the notion that error detection is accomplished by monitoring response conflict via a frontal brain structure, such as the anterior cingulate cortex. We implement this idea in the two-step model of word production, and test the model-derived predictions on a sample of aphasic patients. Our results show a strong correlation between patients ’ error-detection ability and the model’s characterization of their production skills, and no significant correlation between error detection and comprehension measures, thus supporting a production-based monitor, generally, and the implemented conflict-based monitor in particular. The successful application of the conflict-based theory to error-detection in
evidence from invasive electrophysiological
"... accumbens is involved in human action monitoring: ..."

