Common mechanisms in error monitoring and action effect monitoring

In the present study, we considered error-related brain activity in event-related potentials, to investigate the relationship between error monitoring—that is, the detection and evaluation of erroneous responses—and action effect monitoring—that is, monitoring of the sensory consequences of behavior. To this end, participants worked on a task-switching paradigm that consisted of a free-choice task, in which a puzzle piece had to be attached to an existing one (the prime task), and a subsequent color flanker task (the probe task). We examined whether unexpected action effects in the prime task would affect the subsequent error monitoring in the probe task. We found the neural correlates of error monitoring during the probe task, the error-related negativity as well as the error positivity, to be increased after unexpected action effects in the prime task. In contrast, the neural correlates of visual attention were decreased after unexpected action effects, in line with recent findings on an attenuation of sensory processing after errors. Our results demonstrate a direct link between monitoring processes in the two tasks. We propose that both error monitoring and action effect monitoring rely on a common generic monitoring system related to novelty detection or affective processing. Preactivating this system by means of unexpected action effects increases the sensitivity for detecting an error in the subsequent task.     

Metric error monitoring in the numerical estimates

Recent studies have shown that participants can keep track of the magnitude and direction of their errors while reproducing target intervals (Akdoğan & Balcı, 2017) and producing numerosities with sequentially presented auditory stimuli (Duyan & Balcı, 2018). Although the latter work demonstrated that error judgments were driven by the number rather than the total duration of sequential stimulus presentations, the number and duration of stimuli are inevitably correlated in sequential presentations. This correlation empirically limits the purity of the characterization of “numerical error monitoring”. The current work expanded the scope of numerical error monitoring as a form of “metric error monitoring” to numerical estimation based on simultaneously presented array of stimuli to control for temporal correlates. Our results show that numerical error monitoring ability applies to magnitude estimation in these more controlled experimental scenarios underlining its ubiquitous nature.     

Electrophysiological analysis of stimulus variables in equivalence relations

Recently, electrophysiological measures have been used to evaluate the functional overlap between semantic relations and laboratory-defined equivalence relations with abstract stimuli. Several studies using semantic judgment procedures have shown that accompanying EEG-measured neural activity for stimulus pairs from equivalence classes is very similar to that of word pairs from participants' native language. However, those studies often included pronounceable elements (e.g., written nonsense syllables) as at least one member of the experimentally defined classes. The present study conducted EEG studies that contrasted classes with and without such elements. Two groups of undergraduate students completed a matching-to-sample procedure to establish 3 4-member equivalence classes. For Group 1, samples and comparisons were pronounceable pseudowords and abstract figures. For Group 2, the matching-to-sample stimuli were abstract figures only. EEG data recorded during the semantic judgment tasks showed waveform patterns compatible with prior studies of semantic relations in Group 1 but not in Group 2.     

Visuospatial attention in schizophrenia: deficits in broad monitoring

Although selective attention is thought to be impaired in people with schizophrenia (PSZ), prior research has found no deficit in the ability to select one location and withdraw attention from another. PSZ and healthy control subjects (HCS) performed a stimulus detection task in which one, two, or all four peripheral target locations were cued. When one or two locations were cued, both PSZ and HCS responded faster when the target appeared at a cued than uncued location. However, increases in the number of validly cued locations had much more deleterious effects on performance for PSZ than HCS, especially for targets of low contrast whose detection was more dependent on attention. PSZ also responded more slowly in trials with four cued locations relative to trials with one or two invalidly cued locations. Thus, visuospatial attention deficits in schizophrenia arise when broad monitoring is required rather than when attention must be focused narrowly.     

The effects of uncertainty in error monitoring on associated ERPs

A series of experiments were conducted to address the effect of uncertainty regarding performance for predicting the likelihood of a correct-response negativity (CRN) in addition to error-related negativity (ERN). In Study 1, 18 healthy young adults completed letter discrimination tasks during single and dual attention conditions designed to manipulate response certainty. In the second study, the same participants completed easy and difficult tone discrimination tasks designed to influence stimulus certainty. In the third study, task difficulty was manipulated to produce different error rates without altering certainty. Studies 1 and 2 indicated that error and correct responses are processed more similarly when uncertainty is present (i.e., ERN approximately CRN). Furthermore, uncertainty was associated with attenuation of the ERN and enhancement of the CRN, consistent with an error detection hypothesis. Study 3 indicated that task difficulty alone does not influence the ERN or likelihood of a CRN. These results offer support for the error detection account of the ERN and establish the role of uncertainty in predicting the CRN, as postulated by .     

Modeling behavioral measures of error detection in choice tasks: response monitoring versus conflict monitoring

The present study investigated the mechanisms underlying error detection in the error signaling response. The authors tested between a response monitoring account and a conflict monitoring account. By implementing each account within the neural network model of N. Yeung, M. M. Botvinick, and J. D. Cohen (2004), they demonstrated that both accounts make different predictions as to how error signaling performance is influenced by varying the participants' response criterion. These predictions were tested in an experiment using the Eriksen-flanker task. The qualitative pattern as well as a model fit favored the response monitoring account, which states that error detection is mediated by detecting internal error corrections.     

急性应激损伤错误监控与错误后调整

生活中,个体会时时关注自己的行为结果并及时做出调整以适应环境的变化。但在应激下个体能否有效地监控行为并做出适应性调整依然未知。本研究招募了52名男性大学生被试,将其随机分入应激组与控制组,采用特里尔社会应激测试(Trier Social Stress Test, TSST)诱发个体的应激反应,并结合错误意识任务(Error Awareness Task,EAT)探索个体急性应激下的错误监控与错误后调整过程。应激指标的结果显示应激组个体在应激任务后唾液皮质醇、心率、应激感知自我报告和负性情绪均显著高于控制组,表明急性应激的诱发是成功的。行为结果显示应激组的错误意识正确率显著低于控制组,错误意识反应时显著短于控制组;进一步地,应激组个体在意识到错误之后的试次上正确率显著低于未意识到错误之后的试次,并且应激组个体在意识到错误之后的试次上正确率低于控制组。结果表明急性应激降低了个体对错误反应的监控水平,即便在辨别出错误反应的情况下,个体的行为监控与调节也更差。本研究说明急性应激会损伤行为监控系统,导致个体的行为适应性下降。     

Approximation error analysis in bicriteria heuristics

A value structure based on the Tchebycheff measure is proposed to assess the worst-case and average errors in bicriteria heuristics. This analysis builds on earlier results for additive value structures (Daniels, R. L., Manag. Sci., 38 , 501–513 (1992)). The significance of the Tchebycheff measure is that it is representative of a class of quasi-concave functions, and analysis based on this measure is indicative of the performance of the heuristic over a broad range of preference value structures. © 1998 John Wiley & Sons, Ltd.     

Error monitoring dysfunction across the illness course of schizophrenia

Response monitoring abnormalities have been reported in chronic schizophrenia patients, but it is unknown whether they predate the onset of psychosis, are present in early stages of illness, or are late-developing abnormalities associated with illness progression. Response-synchronized event-related potentials (ERP) recorded during a picture-word matching task yielded error-related negativity (ERN), correct-response negativity (CRN), and error positivity (Pe) from 84 schizophrenia patients (SZ), 48 clinical high risk patients (CHR), and their age-matched healthy controls (HC; n = 110 and 88, respectively). A sub-sample of 35 early illness schizophrenia patients (ESZ) was compared to 93 age-matched HC and the CHR patients (after statistically removing the effects of normal aging). Relative to HC, 1) SZ, ESZ, and CHR had smaller ERNs, and 2) SZ and ESZ had larger CRNs and smaller Pes. Within the SZ, longer illness duration was associated with larger CRNs but was unrelated to ERN or Pe. CHR and ESZ did not differ on ERN or CRN, although Pe was smaller in ESZ than CHR. These results indicate that while ERN, CRN, and Pe abnormalities are present early in the illness, only the ERN abnormality is evident prior to psychosis onset, and only the CRN abnormality appears to worsen progressively over the illness course. Brain regions subserving response monitoring may be compromised early in the illness and possibly during its clinical prodrome.     

The relationship between depressive symptoms and error monitoring during response switching

Heightened sensitivity to failure and negative information is thought to be an important maintenance mechanism for symptoms of depression. However, the specific neural and behavioral correlates of the abnormal reactions to errors associated with depression are not yet well understood. The present study was designed to shed new light on this issue by examining how depressive symptoms relate to error monitoring in the context of different task demands. We used a modified flanker task in which the stimulus–response (S–R) mappings were reversed between blocks, differentiating relatively easy nonreversal blocks from the more-demanding S–R reversal blocks. Undergraduates performed this task and then completed a self-report measure of anhedonic depression. The results revealed that depressive symptoms were related to poorer posterror accuracy in the more-difficult S–R reversal blocks, but not in the easier nonreversal blocks. Event-related brain potentials (ERPs) within a subsample of these participants further indicated that depressive symptoms were associated with reduced error positivity (Pe) amplitudes in both block types, suggesting that depressive symptoms were related to reduced attention allocation to errors across the easy and hard blocks. Finally, brain–behavior correlations indicated that highly depressed individuals failed to display a relationship between Pe amplitude and posterror accuracy in the S–R reversal blocks, a relationship that was intact in the low-depression group. Together, these results suggest that task demands play a critical role in the emergence of error-monitoring abnormalities in depression.     

Information-theoretical error analysis of a form-comparison test]

An attempt has been made to make an error analysis, by both the conventional and information theoretical mode of evaluation, of the results of a forms comparison test used for diagnosing the sensory and optical capacity of differentiating. A total of 423 test subjects were available for this program. Data for the standardization of this test and for the evaluation of test results was derived from the results of this investigation.     

The neural basis of error detection: conflict monitoring and the error-related negativity

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.     

Rapid error correction during human arm movements: evidence for central monitoring

Studies were made of rapid error correction movements in eight subjects performing a visually guided tracking task involving flexion-extension movements about the elbow. Subjects were required to minimize reaction times in this two-choice task. Errors in initial movement direction occurred in about 3% of the trials. Error correction times (time from initiation to reversal of movement in incorrect direction) ranged from 30-150 ms. The first sing of correction of the error movement was a suppression of the electromyographic (EMG) activity in the muscle producing the error movement. This suppression started as early as 20-40 ms after the initiation of the error-related EMG activity and as much as 50 ms before any overt sign of limb movement. The correction of the error movement was also accompanied by an increase in the drive to the muscle which moved the arm in the correct direction. This increased activity always occurred after the initiation of the error movement. it is concluded that the first step in the error correction, suppression of drive to the muscle producing the error movement, cannot be based on information from the moving limb. It is thus suggested that this earliest response to the error movement is based on central monitoring of the commands for movement.     

Factor analysis; some effects of chance error

Ignorance concerning the standard error of individual factor loadings and their differences has been a major obstacle to the proper interpretation of factorial results. The effects of three types of experimental error (selection of variables, selection of subjects and selection of scores) are here reported. In order to handle the errors of rotation systematically, it has been necessary to introduce a new semi-analytical criterion for the attainment of simple structure. Variability in results which may theoretically be eliminated is discussed under the heading of non-essential error.     

RT distributional analysis of cognitive-control-related brain activity in first-episode schizophrenia

Impairments in cognitive control are a defining feature of schizophrenia. Aspects of cognitive control include proactive control—the maintenance of task rules or goals to bias attention and maintain preparedness—and reactive control—the engagement of attention in reaction to changing cognitive demands. Proactive control is thought to be particularly impaired in schizophrenia. We sought to examine proactive and reactive control in schizophrenia, as measured by reaction time (RT) variability, and especially long RTs, which are thought to represent lapses in proactive control, during the Stroop paradigm. Furthermore, we sought to examine the neural underpinnings of lapses in proactive control and the subsequent engagement of reactive control in those with schizophrenia, as compared to healthy controls, using fMRI. We found that patients with schizophrenia displayed greater RT variability and more extremely long RTs than controls suggesting that proactive control was weaker in the schizophrenia than in the control group. All of the subjects engaged regions of the cognitive control network during long RTs, consistent with an engagement of reactive control following a failure in proactive control on these trials. The schizophrenia group, however, displayed significantly diminished activity in these regions relative to controls. Our results suggest increased failures in proactive control, but also impaired reactive control, in schizophrenia as compared to healthy subjects.