Abstract
Performance monitoring (PM) is a vital component of adaptive behavior and known to be influenced by motivation. We examined effects of potential gain (PG) and loss avoidance (LA) on neural correlates of PM at different processing stages, using a task with trial-based changes in these motivational contexts. Findings suggest more attention is allocated to the PG context, with higher amplitudes for respective correlates of stimulus and feedback processing. The PG context favored rapid responses, while the LA context emphasized accurate responses. Lower response thresholds in the PG context after correct responses derived from a drift–diffusion model also indicate a more approach-oriented response style in the PG context. This cognitive shift is mirrored in neural correlates: negative feedback in the PG context elicited a higher feedback-related negativity (FRN) and higher theta power, whereas positive feedback in the LA context elicited higher P3a and P3b amplitudes, as well as higher theta power. There was no effect of motivational context on response-locked brain activity. Given the similar frequency of negative feedback in both contexts, the elevated FRN and theta power in PG trials cannot be attributed to variations in reward prediction error. The observed variations in the FRN indicate that the effect of outcome valence is modulated by motivational salience.
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Introduction
Performance monitoring (PM) is the cognitive process of identifying situations where outcomes deviate from intended goals. The purpose of PM is to implement adaptations that compensate current problems and optimize actions in similar situations in the future1,2. PM enables flexibility and adjustments of behavioral strategies according to changing contextual demands. For example, we might be extra careful in a situation where there is much to lose, and behave riskier in situations that offer significant incentives but do not pose any danger. This study examines whether and how PM-related brain activity is affected by changes in motivational context, specifically potential gain and loss avoidance.
The effects of changes in motivational context on behavior have been studied with various task designs that manipulate rewards and feedback3,4,5,6. These manipulations can include block designs as well as trial-by-trial changes in motivational context. Incentive prospect has been associated with better task performance and may be modulated by task-relevant attentional processes6,7,8,9. Reward incentives appear to be most effective in regulating and enhancing cognitive control performance in a proactive and preparatory manner10,11. However, rewards also seem to improve response inhibition without preparatory cues and proactive mechanisms being involved12. Sokol-Hessner and Rutledge13 formulated a model that links dopamine to risk taking for rewards and norepinephrine to loss aversion in punishment. The model predicts that behavior in gain vs. loss contexts is differentially sensitive to manipulations of the dopaminergic and noradrenergic system. The expected value of control (EVC) theory14 suggests that individuals adjust the allocation of control to maximize their expected reward and minimize their expected costs for exerting control. Thus, the adjustment of control strongly depends on motivational factors and therefore it is critical to understand the effects of motivational context on behavior and control allocation15. Rewarding or gain context may invigorate approach behavior, whereas punishment or loss context lead to cautious behavior and avoidance. This has been shown experimentally, where higher rewards resulted in faster responses and higher punishments in higher accuracy16. Contextual factors moderate these mixed or bundled incentive effects, and clear representations of the motivational context aid in determining the control allocation strategy and amount of effort needed to achieve the goal—the same outcome may strengthen or weaken responses, depending on motivational valence and context11,15. Moreover, drift–diffusion models (DDM) provide a useful framework for assessing the influence of different types of incentives (e.g., reward, punishment) on distinct adjustments in control allocation17,18. Examples of this would be higher evidence accumulation rate and lower response threshold for rewarding trials, indicating faster information processing to potentially maximize response rate, and a higher threshold for punishment trials, indicating response caution16. Interestingly, it has been shown that only trial-based changes of motivational context affected performance, as indicated by higher accuracy, in an arrow flanker task19, which is why we manipulated motivational context in a trial-wise fashion in the current study.
In the scalp-recorded event-related potentials, a quite uniform sequence of negative and positive deflections has been found for different situations when adaptation is needed ranging from stimulus, over response to feedback processing2. An early frontocentral sequence of a negative followed by a positive ERP deflection is assumed to be generated at least in part in the posterior medial frontal cortex and associated with a fast alarm signal for the potential necessity for adaptation. This is followed by a more sustained parietal positivity presumably reflecting more elaborated processing of the evaluation signal2. Neural correlates of PM have been shown to be sensitive to motivational context. For stimulus processing, higher N2 amplitudes have been reported in punishment compared to reward motivated trials in a flanker task with trial-by-trial reward manipulation20. Within the punishment context, the P3 also exhibited higher amplitudes for congruent trials than for incongruent trials20. Another study using a Stroop-like task did not observe differences in P3 between trial-by-trial changing contexts21. Regarding response processing, more significant errors, and also higher reward incentives, have been found to be associated with enhancements in error-related negativity (ERN) amplitude—the ERN was therefore suggested to be sensitive to motivation22. Similar results have been found for manipulations of punishment: ERN amplitudes increased in trials with a threat of punishment, compared to neutral trials23,24. When comparing different motivational contexts, results are mixed: in one study using a flanker task with trial-by-trial reward manipulations with the stimulus itself indicating the context, ERN amplitude was reported to be higher in trials with monetary loss than in trials with monetary gain omission20. In another study utilizing a block design in a Simon task, the opposite was reported: the ERN amplitude was higher in the reward block for monetary gain omission than in the punishment block for monetary loss25. Other studies found no difference between reward and punishment contexts for the ERN26,27,28. Aside from the ERN, results on the Pe are also mixed: there are reports of the Pe being larger in reward trials compared to punishment trials, but also reports of no significant differences between Pe in different incentive contexts20,26. The Pe has also been reported to be larger in high punishment contexts compared to low punishment and neutral contexts27. Additionally, there is no evidence of an effect of motivational context on the correct-related negativity [CRN;20,29], a smaller negativity that is observed following correct response execution22,30,31.
Feedback processing is particularly sensitive to motivational context. Here, reward prediction errors (RPE), feedback valence and surprise are likely multiplexed in the FRN32,33,34,35,36,37,38,39,40. The FRN has additionally been found to differ depending on the context of the outcome, with the FRN appearing to correspond to the relative value of the outcome when compared to other potential outcomes, as well as motivational salience40,41,42. Studies suggest that FRN modulations do not depend on whether positive and negative feedback involves gain vs. omitted gain (gain context) or avoided vs. actual loss [punishment context;20,21,25,41,43, but see44]. Interestingly, there have been studies examining the differential influences of feedback magnitudes or valence and expectancy. The FRN was found to be determined by valence as well as expectancy, and to be influenced by valence and magnitude ambiguity38,45,46. FRN amplitudes did not differ between contexts when predictive accuracy was emphasized, but when outcome-valence was highlighted, worse-than-expected outcomes elicited higher amplitudes than better-than-expected outcomes47. This could also explain the conflicting results, aside from different tasks and reward manipulations. The feedback-related P3 also appears to be influenced by gain and loss. The P3 has also been found to be sensitive to magnitude and validity of feedback46,48,49. When contrasting gain and loss contexts, both no differences between contexts and higher amplitudes for actual gain or loss have been reported20,21,43. For comparisons of P3 amplitude in loss, loss avoidance, gain and gain omission, presence or direction of effects also vary between studies20,21,43.
An alternative explanation for the difference in feedback ERPs suggests that the difference reflects variations in reward processing and terms the difference between positive and negative feedback as the reward-related positivity (RewP)50. The RewP has been proposed to reflect a positive RPE signal32,33,51. The RewP has also been linked to motivational factors concerning task performance. It has additionally been shown to be sensitive to differences in reward values associated with different motivational contexts in a gambling task33,52. In recent years, the discussion has also shifted towards integrating ERP analyses with accounts of time–frequency associations and distinguishing between activity for gains and activity for losses, with the ERP measure of the RewP being predicted independently by loss-related theta power and gain-related delta power, with both possibly contributing differently to the ERPs53,54,55,56. Similarly, it has been suggested that the ERPs after feedback result from two overlapping non-valenced RPE magnitude responses: a frontal theta FRN on losses and a posterior delta RewP on wins57. Additionally, frontal midline theta power has been associated with both cognitive effort and the exertion of cognitive control, fitting well into the framework of PM58,59.
The aim of the present study was to examine whether and how PM-related brain activity is influenced by motivational context. Critically, we investigated this with trial-based potential incentives in a potential gain (PG) context and a loss avoidance (LA) context, using electroencephalography (EEG) in a monetary incentive version of the flanker task [see Figure 1;60,61]. We were interested in PM at different stages: stimulus-related (N2, stimulus-P3), response-related (ERN, early and late Pe), and feedback-related activity (FRN, P3a, P3b). We conducted time–frequency analyses for feedback processing, to explore possibly different motivational effects on theta and delta activity. In addition, we examined behavioral effects and used a drift–diffusion model (DDM) to assess the influence of motivational context (e.g., reward, punishment) on distinct adjustments of behavioral control allocation17,18. These analyses were carried out on a dataset that has been analyzed before, with a different focus of analysis [see62]. As the findings on ERPs reported in the literature are very heterogeneous, and as utilized tasks differ substantially, our analyses regarding context effects were exploratory.
Results
Behavioral effects
To assess participants behavior in the task (for a schematic depiction of the task see Fig. 1a) and to examine post-error adjustments like post-error slowing (PES), post-error increase in accuracy (PIA), and post-error speeding for incongruent trials (PERI; post-error reduction of interference)63,64, we conducted two multiple robust single-trial regressions. Errors were defined as actual false responses. We regressed critical task factors onto participant’s single-trial accuracy (GLM1) and reaction time (RT; GLM2) while controlling for confounds and the interdependence of effects, similar to Fischer et al.65. Individual regression weights were then compared using two-sided t-tests corrected for multiple comparisons on group level.
Findings were representative of flanker tasks and additionally reflected effects of motivational context (Fig. 1). Effects of interference were reflected in slower (t129 = 47.93, p < 10–82) and more erroneous (t129 = 17.08, p < 10–33) responses on incongruent trials. PES was reflected in a significant main effect for previous accuracy (t129 = 4.27, p < 10–3). Moreover, there was a general slowing in the LA compared to the PG context (t129 = − 4.92, p < 10–6). Additionally, PIA was present for the PG, but not for the LA context (Fig. 1d, interaction context x previous accuracy t129 = − 2.68, p = 0.049). Errors on the previous trial led to increased accuracy on incongruent, but not congruent trials (Fig. 1, interaction congruency x previous accuracy t129 = − 4.94, p < 10–4).
In a post-task questionnaire, participants also reported that they prioritized accuracy (M = 81.13, SD = 18.30) over speed (M = 73.38, SD = 20.02), z = 4.71, p < 0.001, rc = 0.49, on visual analogue scales. They also reported paying more attention to the green square cueing the PG context (M = 47.38%, SD = 31.22), compared to the red square cueing the LA context (M = 40.16%, SD = 29.38), z = − 3.45, p < 0.01, rc = 0.39. For descriptive RT analyses (see Supplementary Table 1), trials were categorized into post-correct (correct trials following correct trials), pre-error (correct trials before error commission), error, and post-error (correct trials after erroneous response) trials [see66].
Drift–diffusion modelling
In an exploratory analysis, we aimed to parse out the decision process that gives rise to the context dependent behavioral adaptations, by fitting a nested set of different multistage DDMs to task behavior. DDMs provide a framework to investigate distinct adjustments of behavioral control allocation. The details of these models have been describe previously65,67 and are shown in Fig. 2a. The winning model (as measured by the approximated BIC and achieving protected exceedance probabilities (pEP) of 1, see Fig. 2g) was one that included all features (see Fig. 2a for illustration of model features; see Fig. 2b for parameter estimates for the winning model). Sufficiency of the model was evaluated through post predictive checks that matched participants RT and accuracies on various task factors (see Fig. 2c–f). Moreover, parameter recovery analyses revealed that our fit procedure reliably recovered the parameters that generated synthetic data (see Supplementary Fig. 1). Next, we fit the winning model separately to post-error and post-correct trials with positive and negative feedback, respectively, across all contexts and within the PG and LA context. Here, we fixed the variance parameters (sv, sz, st, sf) to the group mean to facilitate convergence. These models captured context-specific RT and accuracies well (see Supplementary Fig. 2). We then used a set of multiple logistic regression of parameter values (drift rate (v), boundary (a), non-decision time (Ter), flanker suppression (f), boundary collapse (k)) onto the trials the model was fitted to, to investigate context related adaptations. Positive regression coefficients indicate parameter increases following errors. We found that Ter was decreased after errors compared to correct responses with positive feedback (β = − 11.61, SE = 5.11, OR = 0.01), Ter was also decreased after errors for the LA context (β = − 12.50, SE = 5.80, OR = 0.01), as was flanker weighting (β = − 1.84, SE = 0.65, OR = 0.16). For PG trials, the same comparison exhibited similar parameter changes for f (β = − 1.32, SE = 0.64, OR = 0.27), and an additional increase in a (β = 3.87, SE = 1.88, OR = 48.02). See Fig. 2h for a visualization. Also, k was decreased after correct trials with negative feedback compared to correct trials with positive feedback (β = 0.50, SE = 0.24, OR = 1.64), which fits with negative feedback in this case signaling responding that was too slow. All other trial types did not differ in fitted parameters. Taken together, context specific adjustments to the decision process were only observed for the boundary (a) which is increased after errors in the PG context. This fits with our other behavioral results showing lower accuracy in general as well as in trials after correct responses in the PG context but no change in accuracy in the LA context, indicating a more cautious response style.
EEG analysis
We employed single-trial robust regression to obtain a regression weight time-course for PM-related EEG activity for all electrodes68. See Table 1 for a summary of regression effects by motivational context.
Stimulus-locked
The stimulus-locked model (with congruency, context and their interaction as predictors within correct trials) revealed a significant effect of context at frontocentral electrodes in a time window corresponding to the P3a (354–492 ms) with the amplitude being more positive in the PG context. There also was a significant effect of context at frontocentral electrodes in the P2 time window (252–274 ms), with the amplitude also being more positive in the PG context69,70. The interaction between congruency and context was not significant. See Fig. 3 for a visualization of results.
Response-locked
The response-locked model (with accuracy, context and their interaction as predictors within incongruent trials) revealed a significant effect of response accuracy, but no covariation of motivational context at frontocentral or parietal electrodes, indicating that ERN, as well as early and late Pe were insensitive to motivational context. There was no significant interaction effect between accuracy and context. See Fig. 4 for a visualization of results.
Feedback-locked
Our analysis of feedback-locked EEG activity (with feedback, context and their interaction as predictors within correct trials) revealed significant effects of feedback type and motivational context at frontocentral electrodes. Notably, time windows corresponding to the P2 (160–210 ms), the FRN (244–286 ms), and the P3a (316–396 ms) were affected. Additionally, there was a significant effect of context at parietal electrodes within the P3b time window (420–548 ms). The interaction between context and feedback was significant at frontocentral electrodes within the FRN time window (218–286 ms) and the P3a time window (316–412 ms), and also at parietal sites within the P3b time window (370–388 ms). No interaction effect was found in the P2 time window.
We further conducted separate follow-up models for positive and negative feedback to investigate their individual contribution. Both models revealed a significant effect of context at frontocentral electrodes for the P2 time window (168–204 ms for negative feedback, and 166–246 ms for positive feedback), indicating larger amplitudes in the PG context. The FRN was significantly larger in the PG context for negative feedback (230–290 ms), but there was no significant effect of context on EEG activity at frontocentral electrodes in a time window corresponding to the FRN for positive feedback. More attention was paid to negative feedback in the PG context (larger P3a; 314–406 ms), whereas more attention was allocated to positive feedback in the LA context (larger P3a; 380–394 ms). The P3b was larger in the LA context for positive feedback (352–600 ms), there was no effect of context for negative feedback.
For a visualization see Figs. 5 and 6. See the Supplement for an analysis of positive vs. negative feedback within each context, and an analysis of feedback after response errors.
Feedback-locked time–frequency analysis
The effects of motivational context were examined for frontocentral theta power following negative and positive feedback, respectively (see Fig. 7 for visualization of effects). For negative feedback, theta power (0–600 ms) was larger in the PG context. There were no effects at parietal electrodes or in the delta range. For positive feedback, frontocentral (240–600 ms) and parietal (28–399 ms) theta power were decreased in the PG context. At FCz, there was a significant increase of delta power (102–195 ms) in the PG context. Direct comparison of negative and positive feedback yielded larger theta as well as delta power for trials with negative feedback (see Supplementary Fig. 3 for effects of different feedback types).
Discussion
The present study examined how neural correlates of PM are influenced by trial-based changes in motivational context. Changes in motivational context shifted the speed-accuracy trade-off towards higher accuracy in the LA and faster responses in the PG context. In the PG context participants could gain points, reacted faster and paid more attention to the target stimulus and the feedback (P2). During response processing, there was no difference between contexts. The negative feedback in the PG context induced the strongest responses (FRN, theta power) and we observed greater adaptation effects within the PG context. There was no context effect of negative feedback for delta power. We therefore identified multiple facets of adaptation in response to changing motivational context.
Behaviorally, slower RTs and overall higher accuracy in the LA context, as well as no change in accuracy between post-correct and post-error trials suggest an especially cautious response style with a higher focus on accuracy than on speed, fitting with predictions by Yee et al. 15. Unexpectedly, there was a decrease in non-decision time after errors: a decrease in this parameter is usually associated with faster stimulus encoding and RT71,72. Potentially, this leads to more accurate responding in the LA context, by increasing efficiency in stimulus encoding. An alternative explanation would be that after positive feedback there is an increase in non-decision time to actively avoid the aversive outcome, which could be connected to higher P3a and P3b in the LA context. For the PG context, faster RT and higher error rate, as well as an increase in accuracy on post-error trials in the PG context, suggest more approach-oriented responding, also in line with Yee et al.15. There also was a difference in decision boundary between post-error and post-correct trials with positive feedback and a PIA effect only found for the PG context. Accuracy and decision boundary were both lower on post-correct trials. Higher decision boundaries are associated with more evidence accumulation before the response and therefore higher accuracy73, indicating less cautious responding in the PG context. However, we did not find the expected difference for drift rate. These effects fit into the EVC theory and its extensions14,15,74, the effects of loss aversion as proposed by Sokol-Hessner and Rutledge13, and the hierarchical reinforcement learning theory of anterior cingulate cortex function34. These models propose more investment of cognitive control when the expected reward is high, and more response caution for potential losses, weighing the cost of effort. Expected reward and efficacy are, according to these theories, weighed against each other and influence behavioral and neural signatures of control allocation and incentive processing75.
We observed larger P2 amplitudes in the PG context during stimulus processing. The P2 is associated with selective attentional processes engaged in evaluating the behavior relevant for adaptive performance based on the stimulus, and important for optimizing the current performance based on that evaluation76,77,78. Similarly, the P3a was also larger in the PG context, which is also associated with attentional processes79,80. This fits with the self-reported attentional bias toward the PG context cue. Together with behavioral findings these observations suggest that participants attributed higher motivational salience towards the PG context.
We found no difference between context for ERPs during response processing (i.e., ERN, CRN and Pe), which is contrary to results from some previous studies that reported changes in ERN amplitude between different motivational contexts [e.g.20,25]. However, this aligns with other research reporting no difference between motivational contexts26. Each of these studies used different tasks and incentive manipulations: be it presenting the contexts in block designs25,26 vs. trial-wise with the stimulus itself indicating the context20; or having deterministic feedback20,26 vs. introducing some uncertainty to the performance feedback by including RT in performance evaluations25. However, there is no apparent pattern in study designs that could explain these differences in results. Changes in response processing depending on motivational context may also express themselves more in the form of general enhancements compared to non-incentive contexts [see23,24,26,27]. Potentially, effects may have also been obscured by participants relying more on external feedback than their motor cues because of the implemented deadline. However, it has been shown in a similar task without motivational contexts that incorrect button presses, but not timing errors (analogue to our task defined by an individual deadline), affected the ERN81; similarly, incorrect button presses influenced the ERN, whereas correct decisions with an action execution worse than expected (spatial accuracy errors, similar to correct trials with slow responses resulting in timing errors) did not82. Importantly, in our analysis, response errors were defined as incorrect button presses, whereas slow responses resulting in timing errors and negative feedback were not included in ERN analysis, making a reliance on motor cues rather than external feedback more likely. Additionally, the processing of deviations between intended and actual response may only be changed for different motivational contexts depending on individual dispositions like compulsivity, conscientiousness and impulsivity23,26,77,83. Further studies are needed to disentangle these connections.
Our findings suggest that feedback processing is influenced by context. Negative feedback elicited higher amplitudes for the FRN and P3a in the PG context, whereas positive feedback elicited more positive P3a and P3b amplitudes in the LA context. Perhaps the most influential hypothesis on the FRN is the account that the FRN might reflect a hierarchical reinforcement learning process34,51: the appropriate task to implement is determined by the anterior cingulate cortex (ACC), then task execution is motivated by applying control over action-production systems, like the basal ganglia, which compute prediction errors (PEs) representing the deviation between expectation and outcome. The PEs are then transmitted to the ACC. The level of control is regulated according to rewards received35,36. Interestingly, the ACC is also proposed to learn reward values of task contexts33,35. RPE signals have been suggested to be modulated by feedback expectancy, have opposite signs for unexpected positive relative to unexpected negative events, and there is increasing evidence for the FRN being an RPE signal32,33. This partially corresponds to our results, with FRN amplitudes being larger for negative feedback. However, the context effect in our study cannot be fully explained by RPE: negative feedback in the PG and the LA context had comparable PE (relative loss of 40 points), and the FRN after response errors was higher in the PG context, despite response errors occurring more frequently. However, there are alternative explanations suggesting the FRN may not reflect the RPE but rather expectancy or surprise37,38. Surprise signals are larger to unexpected relative to expected events, irrespective of outcome valence84. The context effect on FRN in our study can therefore not be fully explained by either: the FRN was larger in the PG context although the frequency of negative feedbacks was similar for both conditions. Potentially, context may influence subjective expectancy of rewarding feedback and thereby affect FRN amplitude: participants may have perceived the PG context as more controllable, and may have consequently had a higher expectancy of positive feedback85,86. All this supports accounts proposing that the FRN is likely the result of multiplexed influences, presumably RPE, the sign or valence of the outcome (irrespective of magnitude), expectancy or surprise, incentive domain (i.e. alternative outcomes) and motivational salience39,40. Stewardson and Sambrook40 propose that the feedback valence, which they define as the sign of the RPE sensitive to the current trial and therefore context dependent, likely overlaps with the motivational salience which results in apparently stronger encoding of valence within the gain domain. The FRN has been shown to be sensitive to the dimension of feedback valence that is most salient [e.g.32,87]. This could explain higher FRN amplitudes for negative feedback within the PG context, even though quantitative RPE and expectancy were matched between PG and LA context. Supporting this, there is a reported attentional bias towards stimuli currently or previously associated with reward88,89,90.
Additionally, frontal midline theta power after negative feedback was higher for the PG vs. LA context, there was no context effect for delta power. Frontal midline theta power has been associated with the exertion of cognitive control during PM58,59. Consistent with this idea, incentive context was shown to influence perceived control: when outcomes were framed as a potential loss, participants significantly lowered their subjective value of control85. The perception of control, in turn, may increase the subjectively estimated probability of a reward, and also how much a reward is subjectively worth. Higher perceived control has been shown to elicit larger FRN and larger differences between reward and non-reward FRN86,91. Consequently, in the PG context the subjective value of positive feedback may have been increased, as may have the subjectively estimated probability of a rewarding feedback: Even though response errors were more frequent in the PG context, the FRN after response errors was still higher compared to the LA context. This process would shift the expectancy of gains, which in turn could explain the FRN amplitude being more sensitive to negative feedback in the PG context.
Limitations of the current study include that the task did not have a non-incentive context. There is evidence that ERPs during response processing are sensitive to incentive contexts as compared to non-incentive ones23,27. Aside from that, context effects might be obscured in tasks with a trial-by-trial compared to a block-wise manipulation because the tasks require constant attention92. Thus, future studies should consider multiple feedback manipulations. Additionally, we had a small number of trials for robust parameter estimation of some of the DDMs93 and introducing response deadlines potentially decreased RT variability, also hindering the detection of differences. We also did not prompt participants to report the prioritization of speed and accuracy separately for motivational context, which would have potentially corroborated the behavioral findings.
To summarize, stimulus- and feedback-locked brain activity was significantly influenced by trial-based manipulation of PG and LA motivational context. Our results suggest that more attention is allocated to the PG context, as evidenced by the stimulus- and feedback-P2, and the stimulus-P3a. Motivational context also affected behavioral performance and feedback processing: In the PG context, responding fast is prioritized, whereas in the LA context, responding accurately is. Negative feedback elicited more negative FRN in the PG context, while positive feedback elicited more positive P3a and P3b in the LA context, possibly signaling for maintenance of response speed and caution. The FRN effect in the current study is likely influenced by motivational salience and subjective probability of rewarding feedback. PG and LA context did not influence response-locked brain activity, although we could not compare the ERPs to a non-incentive condition. Our results demonstrate that motivational context has a significant influence on behavioral responding and performance monitoring during both the stimulus and feedback processing stages.
Methods
Sample
One hundred and forty participants were recruited from the general population in the Dresden, Germany, area. Seven participants committed more than 40% errors across all trials, two had a significant number of random button presses, and another participant discontinued the assessment. They were therefore excluded from further analyses. The final sample consisted of 130 participants (58.5% female; M = 25.88 years, SD = 5.66), 120 participants (92.3%) had completed advanced education degrees, 9.2% reported past mental health problems. Participants self-identified as of mainly European (95.4%) or of mainly Asian (4.6%) ancestry. All participants were native speakers of German, reported no history of head trauma or neurological disease and had normal or corrected-to normal vision. Participants were not included if they reported a history of bipolar disorder; emotionally unstable personality disorder; psychotic episodes; severe alcohol use disorder; currently met the criteria for an eating disorder or severe episode of major depression; reported taking psychotropic substances within the past 3 months; reported a lifetime use of illicit substances of more than twice a year; and lifetime use of cannabis of more than twice a month.
The study was conducted in accordance with the ethical guidelines of the Declaration of Helsinki. The ethics committee at the University Hospital Carl Gustav Carus, Technische Universität Dresden approved study procedures (EK 372092017). All participants gave informed consent. This sample has been analyzed before with a different focus of analysis [see62].
Procedure, measures and tasks
Procedure
Participants took part in two sessions in the lab, and between those sessions a week of ecological momentary assessment. The effect of reward and punishment on PM-related brain activity was assessed during a monetary incentive flanker task using EEG during the second session. The EEG session took place a minimum of 8 days after the first session. During both sessions, participants performed other tasks, which are not part of this report.
Monetary incentive flanker task
A modified version of the arrow-version of the Eriksen flanker task, with a potential gain (PG) and a loss avoidance (LA) incentive context, was employed60,61. Participants had to respond as quickly and correctly as possible using a left or right button, according to the direction of the centrally presented target arrow. The target stimulus appeared for 30 ms, with a delay of 100 ms relative to the onset of the surrounding flanker arrows. In 50% of the trials, the target stimulus pointed in the opposite direction (incongruent) as the flanker arrows. In the other 50% of the trials, the target pointed in the same direction (congruent). Each trial started with an incentive cue, signaling potential gain or loss of 40 points in the current trial. The incentive cue, a red (LA) or green (PG) frame surrounding a fixation cross, was presented for 500 ms. The frame remained visible for the duration of the trial. After response, feedback on task performance was presented: negative feedback was presented for incorrect and the slowest 20% of the correct responses and positive feedback for the remaining correct responses. In the LA context (50% of the trials) negative feedback was associated with a loss of 40 points and positive feedback with loss omission (0 points). In the PG context positive feedback resulted in a gain of 40 points and negative feedback in reward omission (0 points). An adaptive deadline based on individual performance and response time determined the response deadline, in order to approach a rate of 20% negative feedback for each context (PG context: M = 18.6%, SD = 2.3%; LA context: M = 19.6%, SD = 2.3%). After a response interval of 900 ms following target onset or 600 ms after response, performance feedback was presented for 800 ms. Participants could earn a bonus of up to 5 EUR, depending on task performance and points earned. The task included 640 trials of 2.53–2.75 s duration and an additional training block of 40 trials. Task duration was approximately 25 min. After task completion, participants were asked, on a visual analogue scale, how important it was to them to respond accurately, how important it was for them to respond fast, and how much attention they paid to the red and the green frame, respectively. The task was presented using Presentation 19.0 (Neurobehavioral Systems Inc., Berkeley, CA, USA). See Fig. 1a for a schematic depiction of the task.
Psychophysiological recording and data reduction
The EEG was continuously recorded using elastic EEG caps with 63 Ag/AgCl electrodes at equidistant locations (EasyCap GmbH, Herrsching-Breitbrunn, Germany) and two 32-channel BrainAmp amplifiers (Brain Products GmbH, Munich, Germany) at a sampling rate of 500 Hz. Impedances were kept below 10 kOhm. Eye movement was captured using two external electrodes placed below the left and right eye together with electrodes above both and lateral to both eyes mounted into the cap. Ground and reference electrodes were placed next to Fz (at AFF1h and AFF2h, theta/phi spherical coordinates: − 58/78 and 58/78). The EEG was high and low pass filtered with cutoffs of 0.1 and 30 Hz, respectively, and epoched from –500 to 2000 ms relative to target stimulus onset. Epochs with artifacts were rejected automatically based on signal deviations greater than 5 SD of the mean probability distribution on any single channel or the whole montage. Remaining epochs were demeaned and submitted to adaptive mixture independent component analysis (AMICA), implemented in EEGLAB 14.1.294. Independent components reflecting ocular or cardiovascular artifacts were removed manually and EEG data were re-referenced to common average reference. Subsequently, target stimulus-locked, response-locked and feedback-locked epochs from − 500 to 1000 ms were created. The average EEG activity 200–0 ms prior to stimulus, response and feedback was used as baseline, respectively. Offline analyses were performed using EEGLAB 14.1.294 and MATLAB 2018b95. Data were then further analyzed using multiple robust single-trial regression analyses [e.g.68,96].
Data analysis
Behavioral data
We employed two multiple robust regression models onto each participant’s single-trial accuracy and log-transformed reaction time (RT) to determine predictors of influence65. The RT model was specified as follows: log(RT) = b0 + congruency x b1 + previous accuracy x b2 + context x b3 + accuracy x b4 + trial x b5 + e. The logistic accuracy model was specified by: accuracy = b0 + congruency x b1 + previous accuracy x b2 + context x b3 + trial x b4 + e. The predictors are: congruency (congruency between flanker and target; − 1 = congruent, 1 = incongruent), previous accuracy (accuracy of the immediately preceding trial; − 1 = correct, 1 = error), context (incentive context of the current trial; − 1 = LA, 1 = PG), accuracy (of the current trial; − 1 = correct, 1 = error) and trial (trial number, reflecting the time on the task). Trial mainly served to control for unspecific effects of task duration (e.g. adjustments of speed-accuracy trade-offs over the task or blocks, or fatigue). Individual t-values per regressor were tested via two-sided t-tests against zero, on group level, all p-values were Bonferroni corrected. Follow-up analyses are shown in respective figures (Fig. 1).
Because the self-report data were not normally distributed as determined by the Shapiro–Wilk test of normality (of the differences), we analyzed differences between behavioral measures using the Wilcoxon signed rank test97,98. P values were adjusted for multiple comparisons using the procedure proposed by Benjamini and Yekutieli99.
Drift–diffusion modelling
Features of the multi-stage sequential sampling models and general fitting procedures were exactly as described by Fischer et al.65 and Kirschner et al.67. The description is adapted from therein. We used a multi-stage sequential sampling model to simulate participants' RT and accuracy distributions and the decision process giving rise to these. The model approximates the decision process as a single decisions variable which reflects both decision options. We previously demonstrated that this approximation is valid and compatible with an independently measured neural decision signal (i.e., lateralized movement selective beta power (BPL))65,67. The discrete diffusion model simulates decisions as a Wiener process with stepwise increments according to a Gaussian distribution with mean v (called drift rate) and variance s on every trial. Here, v reflects the speed of evidence accumulation and s the system’s noise, which scales all other parameters and is usually fixed (here to 0.1). The step size for all models was set to 1 ms. Responses are triggered when the diffusion reaches a criterion (boundary, determined by the free parameter ± a). We assumed that there was no bias in response selection over the task, because we had an equal number of left and right responses. However, individual trials were allowed to start with a random bias towards one response (start-point variability, parameter sz). We used symmetrical boundaries which were defined as left-hand responses when the positive boundary was reached first, and as right-hand responses when the negative boundary was reached first (see Fig. 2a for more details). The non-decision time was modelled as another free parameter Ter. The stages of the model per trial were defined as a zero-mean baseline until flanker onset, a noisy diffusion with v = 0 during the non-decision time, a diffusion driven by the flanker direction between flanker and target onset (100 ms) with drift = vt × ft, and the target phase thereafter with drift = vt and the direction of the target. Single-trial values vt and ft were determined according to Gaussian variance parameters sv and sf. For display purposes, in Fig. 2a, we modelled a consecutive return of the decision variable to baseline like an Ornstein–Uhlenbeck process. To speed up the model fitting procedure, we did neither simulate baseline periods nor return to baseline during the fitting because these have no effect on model predictions. We compared four different variants of the DDM by fitting their parameters to RT and accuracy data observed in the group of 130 participants using quantile maximum likelihood statistics100 and differential evolution algorithms101. Additionally, we used a mixture model assuming 2% outliers that were distributed uniformly over the full range of RTs in correct and error responses. This downweighs the impact of possible outliers on model parameters. DDM model 1 used the same drift rate during flanker and target processing, thus not allowing for suppression of distractors (parameter f fixed to 1). DDM model 2 fixed parameter f which suppressed flanker processing when below the value of 1. DDM model 3 furthermore included trial-by-trial variance in f modelled as a zero-mean Gaussian distribution with variance sf. The fourth DDM model extended DDM model 3 to allow for a dynamic decision boundary collapse according to a Weibull distribution scaled by the free parameter k. Here, the dynamic boundary u at time t was calculated as follows:
In this equation, \({\varvec{a}}\) represents the initial boundary value and \({\varvec{k}}\) scales the Weibull distribution. The shape parameter \({\varvec{s}}\) was fixed at 3, to impose a “late collapse” decision strategy.
For model fitting in all iterations, we applied the following hard priors which can be seen as boundary parameters: v [0.01–8.5], sv [0–1.5], a [0.01–0.45], sz [0.05–0.3], Ter [0.1–0.4], st [0–2], f [0.1–1.5], sf [0–1.5], k [10e-4–3].
For model comparison, we first computed approximated BIC values (aBIC; akin to White et al.102). Next, we used these individual aBIC values to compute protected exceedance probabilities, which gives the probability that one model was more likely than any other model of the model space Rigoux et al.103. As DDM4 provided the best fit to the data, we used this model to investigate model parameters when this model was fit separately to post-error and post-correct trials with positive and negative feedback, respectively, across all contexts and additionally within the PG and LA context. For this analysis, we fixed the variance parameters (sv, sz, st, sf) to the group mean to facilitate convergence.
To simulate the temporal evolution of the modelled diffusion signal depicted in Fig. 2a we used the mean maximum likelihood parameters from the group fit obtained for DDM4. For this simulation, we computed 5000 simulated trials.
EEG analyses
Multiple robust regression104 was employed to build a general linear model (GLM) and regress behavioral and task parameters on single-trial EEG activity at each electrode and time point. The resulting individual b values were standardized by their SDs before averaging across subjects, to penalize the regression model in case of multicollinearity of predictors and ensure comparability between predictors.
Stimulus-locked analyses
The model for target stimulus-locked EEG included only correct trials and included a regressor coding the incentive context of the current trial (loss/gain), the interaction between context and congruency of the current trial, the congruency (congruent/incongruent) of the current trial, the accuracy of the previous trial (correct/error) and log scaled RT.
Response-locked analyses. We built a model for response-locked EEG, which only included incongruent trials. The model included a regressor coding the accuracy of the current trial (correct/error), incentive context of the current trial (loss/gain) and the interaction between accuracy and context of the current trial. Log scaled RT of the current trial and response hand (left/right) were included as additional regressors.
Feedback-locked analyses
We focused our data analysis on feedback after correct responses, as only feedback after correct responses carried new information and erroneous responses deterministically elicited negative feedback. The first feedback model included the regressors coding the incentive context of the current trial (loss/gain), the feedback valence (negative/positive), and the interaction between feedback and context. To follow-up the interaction, we built two additional models for correct trials with corresponding positive feedback and for correct trials with negative feedback, respectively. Both models included the incentive context of the current trial (loss/gain) as the only regressor. See the Supplement for an analysis of error trials and corresponding negative feedback, a cue-locked analysis, as well as the effect of feedback type within the respective context.
The standardized b values resulting from the models were tested using two-tailed one-sample t-tests, for FCz and Pz. The tests were done for each data point across subjects. The resulting p values were adjusted for multiple comparisons using the false discovery rate (FDR) procedure proposed by Benjamini and Yekutieli99. We set a criterion value of 0.001 to minimize the chance of false positive results. The FDR procedure by Benjamini and Yekutieli99 has been found to facilitate good control of the family-wise error rate (FWER) in EEG data105. As FDR does not provide sound local control of the FWER, FDR was applied per model and electrode. H0 was rejected for p < 2.2654e−4 (FCz) and p < 3.2189e−4 (Pz) in the stimulus-locked, for p < 2.8827e−4 (FCz) and p < 3.4804e−4 (Pz) in the response-locked model, for p < 3.7708e−4 (FCz) and p < 2.7407e−4 (Pz) in the first feedback-locked model, for p < 1.9288e−4 (FCz) and p < 4.2192e−4 (Pz) in the feedback-locked model for correct trials with corresponding positive feedback and for p < 2.2664e−4 (FCz) and p < 2.1000e−5 (Pz) for the feedback-locked model for correct trials with negative feedback.
Time–frequency analysis of feedback
We also analyzed feedback-locked activity in the time–frequency domain, to investigate whether possible differences between contexts were due to theta- or delta-band activity. Analyses were conducted according to recommendations by Cohen106. Data were epoched around the feedback onset (− 1000 to 2000 ms). The interval between − 500 to − 200 ms was used for baseline correction. Time–frequency decomposition was done separately for each combination of feedback type and context. EEG time series in each epoch were convolved with a set of complex Morlet wavelets, defined as a Gaussian-windowed complex sine wave: \({\mathrm{e}}^{-\mathrm{i}2\mathrm{\pi ft}}{e}^{ \frac{-4{\mathrm{log}(2)t}^{2}}{{h}^{2}}}\), where t is time, f is frequency, which increased from 1 to 20 Hz in 20 logarithmically spaced steps, and h defines the full-width at half-maximum, which ranged from 600 to 300 ms with 20 logarithmically spaced steps107. Power was normalized by conversion to a decibel (dB) scale (10 ∗ log10[power(t)/power(baseline)]), to allow direct comparison of effects across frequency bands. Each epoch was then cut to − 200 to 600 ms. Epochs were then averaged for each context, feedback type and participant. The differences between the PG and LA contexts were tested using two-tailed one-sample t-tests, for FCz and Pz. The tests were done for each data point across subjects, within a time window from 0 to 600 ms and frequencies between 1 and 8, to include delta and theta bands. Differences between contexts were tested for negative and positive feedback separately. The resulting p values were adjusted for multiple comparisons using the FDR procedure proposed by Benjamini and Yekutieli99. We set a criterion value of 0.001 to minimize the chance of false positive results. H0 was rejected for p < 4.6630e−4 (FCz) and p < 1.1885e−7 (Pz) for the comparison of contexts in negative feedback, and for p < 1.9453e−4 (FCz) and p < 6.6510e−5 (Pz) for the comparison of contexts in positive feedback.
Statistical analysis of EEG and behavioral data was performed in MATLAB 2018b95 and R 4.2.0108.
Data availability
The data that support the findings of this study are available on OSF (https://osf.io/h6ju7/) and from the corresponding author on request.
References
Ullsperger, M., Danielmeier, C. & Jocham, G. Neurophysiology of performance monitoring and adaptive behavior. Physiol. Rev. 94, 35–79 (2014).
Ullsperger, M., Fischer, A. G., Nigbur, R. & Endrass, T. Neural mechanisms and temporal dynamics of performance monitoring. Trends Cogn. Sci. 18, 259–267 (2014).
van Steenbergen, H., Band, G. P. & Hommel, B. Reward counteracts conflict adaptation: Evidence for a role of affect in executive control. Psychol. Sci. 20, 1473–1477 (2009).
van Steenbergen, H., Band, G. P. & Hommel, B. Reward valence modulates conflict-driven attentional adaptation: Electrophysiological evidence. Biol. Psychol. 90, 234–241 (2012).
Braem, S., Verguts, T., Roggeman, C. & Notebaert, W. Reward modulates adaptations to conflict. Cognition 125, 324–332 (2012).
Krebs, R. M. & Woldorff, M. G. Cognitive control and reward (2017).
Pessoa, L. & Engelmann, J. B. Embedding reward signals into perception and cognition. Front. Neurosci. 4, 17 (2010).
van den Berg, B., Krebs, R. M., Lorist, M. M. & Woldorff, M. G. Utilization of reward-prospect enhances preparatory attention and reduces stimulus conflict. Cogn. Affect. Behav. Neurosci. 14, 561–577 (2014).
Seifert, J., Naumann, E., Hewig, J., Hagemann, D. & Bartussek, D. Motivated executive attention—Incentives and the noise-compatibility effect. Biol. Psychol. 71, 80–89 (2006).
Goschke, T. & Bolte, A. Emotional modulation of control dilemmas: The role of positive affect, reward, and dopamine in cognitive stability and flexibility. Neuropsychologia 62, 403–423 (2014).
Yee, D. M. & Braver, T. S. Interactions of motivation and cognitive control. Curr. Opin. Behave. Sci. 19, 83–90 (2018).
Boehler, C. N., Schevernels, H., Hopf, J.-M., Stoppel, C. M. & Krebs, R. M. Reward prospect rapidly speeds up response inhibition via reactive control. Cogn. Affect. Behav. Neurosci. 14, 593–609 (2014).
Sokol-Hessner, P. & Rutledge, R. B. The psychological and neural basis of loss aversion. Curr. Dir. Psychol. Sci. 28, 20–27 (2019).
Shenhav, A., Botvinick, M. M. & Cohen, J. D. The expected value of control: An integrative theory of anterior cingulate cortex function. Neuron 79, 217–240 (2013).
Yee, D. M., Leng, X., Shenhav, A. & Braver, T. S. Aversive motivation and cognitive control. Neurosci. Biobehav. Rev. (2021).
Leng, X., Yee, D., Ritz, H. & Shenhav, A. Dissociable influences of reward and punishment on adaptive cognitive control. PLoS Comput. Biol. 17, e1009737 (2021).
Ratcliff, R. & McKoon, G. The diffusion decision model: Theory and data for two-choice decision tasks. Neural Comput. 20, 873–922 (2008).
Ratcliff, R., Smith, P. L., Brown, S. D. & McKoon, G. Diffusion decision model: Current issues and history. Trends Cogn. Sci. 20, 260–281 (2016).
Kostandyan, M. et al. Differential effects of sustained and transient effort triggered by reward–A combined EEG and pupillometry study. Neuropsychologia 123, 116–130 (2019).
Potts, G. F. Impact of reward and punishment motivation on behavior monitoring as indexed by the error-related negativity. Int. J. Psychophysiol. 81, 324–331 (2011).
Carsten, T., Kostandyan, M., Boehler, C. N. & Krebs, R. M. Comparing the motivational value of rewards and losses in an EEG-pupillometry study. Eur. J. Neurosci. 53, 1822–1838 (2021).
Hajcak, G., Moser, J. S., Yeung, N. & Simons, R. F. On the ERN and the significance of errors. Psychophysiology 42, 151–160 (2005).
Endrass, T. et al. Performance monitoring and error significance in patients with obsessive-compulsive disorder. Biol. Psychol. 84, 257–263 (2010).
Riesel, A., Weinberg, A., Endrass, T., Kathmann, N. & Hajcak, G. Punishment has a lasting impact on error-related brain activity. Psychophysiology 49, 239–247 (2012).
Stürmer, B., Nigbur, R., Schacht, A. & Sommer, W. (2011).
Maruo, Y., Schacht, A., Sommer, W. & Masaki, H. Impacts of motivational valence on the error-related negativity elicited by full and partial errors. Biol. Psychol. 114, 108–116 (2016).
Maruo, Y., Sommer, W. & Masaki, H. The effect of monetary punishment on error evaluation in a Go/No-go task. Int. J. Psychophysiol. 120, 54–59 (2017).
Willems, A. L., Jelinčić, V., Vlaeyen, J. W., von Leupoldt, A. & Torta, D. M. Is it a painful error? The effect of unpredictability and intensity of punishment on the error-related negativity, and somatosensory evoked potentials. Biol. Psychol. 108177 (2021).
Boksem, M. A. S., Tops, M., Kostermans, E. & De Cremer, D. Sensitivity to punishment and reward omission: Evidence from error-related ERP components. Biol. Psychol. 79, 185–192. https://doi.org/10.1016/j.biopsycho.2008.04.010 (2008).
Ford, J. M. Schizophrenia: The broken P300 and beyond. Psychophysiology 36, 667–682 (1999).
Endrass, T., Klawohn, J., Gruetzmann, R., Ischebeck, M. & Kathmann, N. Response-related negativities following correct and incorrect responses: Evidence from a temporospatial principal component analysis. Psychophysiology 49, 733–743 (2012).
Sambrook, T. D. & Goslin, J. A neural reward prediction error revealed by a meta-analysis of ERPs using great grand averages. Psychol. Bull. 141, 213 (2015).
Umemoto, A., HajiHosseini, A., Yates, M. E. & Holroyd, C. B. Reward-based contextual learning supported by anterior cingulate cortex. Cogn. Affect. Behav. Neurosci. 17, 642–651 (2017).
Holroyd, C. B. & Yeung, N. Motivation of extended behaviors by anterior cingulate cortex. Trends Cogn. Sci. 16, 122–128 (2012).
Holroyd, C. B. & McClure, S. M. Hierarchical control over effortful behavior by rodent medial frontal cortex: A computational model. Psychol. Rev. 122, 54 (2015).
Shahnazian, D. & Holroyd, C. B. Distributed representations of action sequences in anterior cingulate cortex: A recurrent neural network approach. Psychon. Bull. Rev. 25, 302–321 (2018).
Talmi, D., Atkinson, R. & El-Deredy, W. The feedback-related negativity signals salience prediction errors, not reward prediction errors. J. Neurosci. 33, 8264–8269 (2013).
Hauser, T. U. et al. The feedback-related negativity (FRN) revisited: New insights into the localization, meaning and network organization. Neuroimage 84, 159–168 (2014).
Kirsch, F., Kirschner, H., Fischer, A. G., Klein, T. A. & Ullsperger, M. Disentangling performance-monitoring signals encoded in feedback-related EEG dynamics. NeuroImage 257, 119322 (2022).
Stewardson, H. & Sambrook, T. D. Valence precedes value in neural encoding of prediction error. Psychophysiology e14266 (2023).
Holroyd, C. B., Larsen, J. T. & Cohen, J. D. Context dependence of the event-related brain potential associated with reward and punishment. Psychophysiology 41, 245–253 (2004).
Hajcak, G., Holroyd, C. B., Moser, J. S. & Simons, R. F. Brain potentials associated with expected and unexpected good and bad outcomes. Psychophysiology 42, 161–170 (2005).
Pfabigan, D. M. et al. Context-sensitivity of the feedback-related negativity for zero-value feedback outcomes. Biol. Psychol. 104, 184–192 (2015).
Hämmerer, D., Li, S.-C., Müller, V. & Lindenberger, U. Life span differences in electrophysiological correlates of monitoring gains and losses during probabilistic reinforcement learning. J. Cogn. Neurosci. 23, 579–592 (2011).
Gu, R. et al. Valence and magnitude ambiguity in feedback processing. Brain Behav. 7, e00672 (2017).
Kirschner, H., Fischer, A. G. & Ullsperger, M. Feedback-related EEG dynamics separately reflect decision parameters, biases, and future choices. NeuroImage 259, 119437 (2022).
Gu, Y. et al. The event-related potentials responding to outcome valence and expectancy violation during feedback processing. Cereb. Cortex 31, 1060–1076 (2021).
Wischnewski, M. & Schutter, D. J. Dissociating absolute and relative reward-and punishment-related electrocortical processing: An event-related potential study. Int. J. Psychophysiol. 126, 13–19 (2018).
Pietschmann, M., Endrass, T., Czerwon, B. & Kathmann, N. Aging, probabilistic learning and performance monitoring. Biol. Psychol. 86, 74–82 (2011).
Holroyd, C. B., Pakzad-Vaezi, K. L. & Krigolson, O. E. The feedback correct-related positivity: Sensitivity of the event-related brain potential to unexpected positive feedback. Psychophysiology 45, 688–697 (2008).
Holroyd, C. B. & Coles, M. G. The neural basis of human error processing: Reinforcement learning, dopamine, and the error-related negativity. Psychol. Rev. 109, 679 (2002).
Holroyd, C. B. & Umemoto, A. The research domain criteria framework: The case for anterior cingulate cortex. Neurosci. Biobehav. Rev. 71, 418–443 (2016).
Proudfit, G. H. The reward positivity: From basic research on reward to a biomarker for depression. Psychophysiology 52, 449–459 (2015).
Foti, D., Weinberg, A., Bernat, E. M. & Proudfit, G. H. Anterior cingulate activity to monetary loss and basal ganglia activity to monetary gain uniquely contribute to the feedback negativity. Clin. Neurophysiol. 126, 1338–1347 (2015).
Williams, C. C., Ferguson, T. D., Hassall, C. D., Abimbola, W. & Krigolson, O. E. The ERP, frequency, and time–frequency correlates of feedback processing: Insights from a large sample study. Psychophysiology 58, e13722 (2021).
Bernat, E. M., Nelson, L. D. & Baskin-Sommers, A. R. Time-frequency theta and delta measures index separable components of feedback processing in a gambling task. Psychophysiology 52, 626–637 (2015).
Hoy, C. W., Steiner, S. C. & Knight, R. T. Single-trial modeling separates multiple overlapping prediction errors during reward processing in human EEG. Commun. Biol. 4, 1–17 (2021).
Wascher, E. et al. Frontal theta activity reflects distinct aspects of mental fatigue. Biol. Psychol. 96, 57–65 (2014).
Jensen, O. & Tesche, C. D. Frontal theta activity in humans increases with memory load in a working memory task. Eur. J. Neurosci. 15, 1395–1399 (2002).
Eriksen, B. A. & Eriksen, C. W. Effects of noise letters upon the identification of a target letter in a nonsearch task. Percept. Psychophys. 16, 143–149 (1974).
Kopp, B., Rist, F. & Mattler, U. N200 in the flanker task as a neurobehavioral tool for investigating executive control. Psychophysiology 33, 282–294 (1996).
Overmeyer, R. et al. The error-related negativity predicts self-control failures in daily life. Front. Hum. Neurosci. 14, 616 (2021).
Ridderinkhof, K. R. et al. Alcohol consumption impairs detection of performance errors in mediofrontal cortex. Science 298, 2209–2211 (2002).
Danielmeier, C. & Ullsperger, M. Post-error adjustments. Front. Psychol. 2, 233 (2011).
Fischer, A. G., Nigbur, R., Klein, T. A., Danielmeier, C. & Ullsperger, M. Cortical beta power reflects decision dynamics and uncovers multiple facets of post-error adaptation. Nat. Commun. 9, 1–14 (2018).
Danielmeier, C., Eichele, T., Forstmann, B. U., Tittgemeyer, M. & Ullsperger, M. Posterior medial frontal cortex activity predicts post-error adaptations in task-related visual and motor areas. J. Neurosci. 31, 1780–1789 (2011).
Kirschner, H., Fischer, A. G., Danielmeier, C., Klein, T. A. & Ullsperger, M. Cortical beta power reflects a neural implementation of decision boundary collapse in a speeded flanker task. bioRxiv, 2023.2001. 2013.523918 (2023).
Fischer, A. G. & Ullsperger, M. Real and fictive outcomes are processed differently but converge on a common adaptive mechanism. Neuron 79, 1243–1255 (2013).
Potts, G. F. An ERP index of task relevance evaluation of visual stimuli. Brain Cogn. 56, 5–13 (2004).
Luck, S. J. & Hillyard, S. A. Electrophysiological correlates of feature analysis during visual search. Psychophysiology 31, 291–308 (1994).
White, C. N., Ratcliff, R., Vasey, M. W. & McKoon, G. Using diffusion models to understand clinical disorders. J. Math. Psychol. 54, 39–52 (2010).
Mulder, M. J. & van Maanen, L. Are accuracy and reaction time affected via different processes? PLoS One 8, e80222 (2013).
Purcell, B. A. & Kiani, R. Neural mechanisms of post-error adjustments of decision policy in parietal cortex. Neuron 89, 658–671 (2016).
Shenhav, A., Cohen, J. D. & Botvinick, M. M. Dorsal anterior cingulate cortex and the value of control. Nat. Neurosci. 19, 1286–1291 (2016).
Frömer, R., Lin, H., Dean Wolf, C., Inzlicht, M. & Shenhav, A. Expectations of reward and efficacy guide cognitive control allocation. Nat. Commun. 12, 1–11 (2021).
Gajewski, P. D., Stoerig, P. & Falkenstein, M. ERP—Correlates of response selection in a response conflict paradigm. Brain Res. 1189, 127–134 (2008).
Potts, G. F., George, M. R. M., Martin, L. E. & Barratt, E. S. Reduced punishment sensitivity in neural systems of behavior monitoring in impulsive individuals. Neurosci. Lett. 397, 130–134 (2006).
Rey-Mermet, A., Gade, M. & Steinhauser, M. Sequential conflict resolution under multiple concurrent conflicts: An ERP study. NeuroImage 188, 411–418 (2019).
Polich, J. Updating P300: An integrative theory of P3a and P3b. Clin. Neurophysiol. 118, 2128–2148 (2007).
Katayama, J. I. & Polich, J. Stimulus context determines P3a and P3b. Psychophysiology 35, 23–33 (1998).
Stahl, J. Error detection and the use of internal and external error indicators: An investigation of the first-indicator hypothesis. Int. J. Psychophysiol. 77, 43–52. https://doi.org/10.1016/j.ijpsycho.2010.04.005 (2010).
Bediou, B., Koban, L., Rosset, S., Pourtois, G. & Sander, D. Delayed monitoring of accuracy errors compared to commission errors in ACC. Neuroimage 60, 1925–1936. https://doi.org/10.1016/j.neuroimage.2012.02.010 (2012).
Pailing, P. E. & Segalowitz, S. J. The error-related negativity as a state and trait measure: Motivation, personality, and ERPs in response to errors. Psychophysiology 41, 84–95 (2004).
Sutton, R. S. & Barto, A. G. Introduction to Reinforcement Learning (1998).
Wang, K. S., Kashyap, M. & Delgado, M. R. The influence of contextual factors on the subjective value of control. Emotion (2020).
Mühlberger, C., Angus, D. J., Jonas, E., Harmon-Jones, C. & Harmon-Jones, E. Perceived control increases the reward positivity and stimulus preceding negativity. Psychophysiology 54, 310–322 (2017).
Nieuwenhuis, S., Yeung, N., Holroyd, C. B., Schurger, A. & Cohen, J. D. Sensitivity of electrophysiological activity from medial frontal cortex to utilitarian and performance feedback. Cereb. Cortex 14, 741–747 (2004).
Anderson, B. A., Laurent, P. A. & Yantis, S. Reward predictions bias attentional selection. Front. Hum. Neurosci. 7, 262 (2013).
Anderson, B. A. et al. Linking dopaminergic reward signals to the development of attentional bias: A positron emission tomographic study. NeuroImage 157, 27–33 (2017).
Jones, A. et al. Reward expectancy promotes generalized increases in attentional bias for rewarding stimuli. Q. J. Exp. Psychol. 65, 2333–2342 (2012).
Warren, C. M. & Holroyd, C. B. The impact of deliberative strategy dissociates ERP components related to conflict processing vs. reinforcement learning. Front. Neurosci. 6, 43 (2012).
Tullo, D., Perico, C., Faubert, J. & Bertone, A. Multiple object-tracking isolates feedback-specific load in attention and learning. J. Vis. 20, 9–9 (2020).
Lerche, V., Voss, A. & Nagler, M. How many trials are required for parameter estimation in diffusion modeling? A comparison of different optimization criteria. Behav. Res. Methods 49, 513–537 (2017).
Delorme, A. & Makeig, S. EEGLAB: An open source toolbox for analysis of single-trial EEG dynamics including independent component analysis. J. Neurosci. Methods 134, 9–21 (2004).
MATLAB v. version 9.5.0.944444 (R2018b) (Natick, Massachusetts, USA, 2018).
Fischer, A. G., Endrass, T., Reuter, M., Kubisch, C. & Ullsperger, M. Serotonin reuptake inhibitors and serotonin transporter genotype modulate performance monitoring functions but not their electrophysiological correlates. J. Neurosci. 35, 8181–8190 (2015).
Wilcoxon, F. Individual comparisons by ranking methods. Biom. Bull. 1, 80–83. https://doi.org/10.2307/3001968 (1945).
Shapiro, S. S. & Wilk, M. B. An analysis of variance test for normality (complete samples)†. Biometrika 52, 591–611. https://doi.org/10.1093/biomet/52.3-4.591 (1965).
Benjamini, Y. & Yekutieli, D. The control of the false discovery rate in multiple testing under dependency. Ann. Stat. 1165–1188 (2001).
Heathcote, A., Brown, S. & Cousineau, D. QMPE: Estimating Lognormal, Wald, and Weibull RT distributions with a parameter-dependent lower bound. Behav. Res. Methods Instrum. Comput. 36, 277–290 (2004).
Price, K. V. et al. Parallel differential evolution: Application to 3-d medical image registration. Differ. Evol. A Pract. Approach Glob. Optim. 353–411 (2005).
White, C. N., Ratcliff, R. & Starns, J. J. Diffusion models of the flanker task: Discrete versus gradual attentional selection. Cogn. Psychol. 63, 210–238 (2011).
Rigoux, L., Stephan, K. E., Friston, K. J. & Daunizeau, J. Bayesian model selection for group studies—Revisited. Neuroimage 84, 971–985 (2014).
O’Leary, D. P. Robust regression computation using iteratively reweighted least squares. SIAM J. Matrix Anal. Appl. 11, 466–480 (1990).
Groppe, D. M., Urbach, T. P. & Kutas, M. Mass univariate analysis of event-related brain potentials/fields I: A critical tutorial review. Psychophysiology 48, 1711–1725 (2011).
Cohen, M. X. Analyzing Neural Time Series Data: Theory and Practice (MIT Press, 2014).
Cohen, M. X. A better way to define and describe Morlet wavelets for time-frequency analysis. NeuroImage 199, 81–86 (2019).
R: A language and environment for statistical computing (R Foundation for Statistical Computing, 2022).
Acknowledgements
The authors would like to thank Julia Berghäuser for her contribution to data collection. The authors express their gratitude to all participants for their time and cooperation. We thank the Center for Information Services and High Performance Computing (ZIH) at TU Dresden for generous allocations of computer time.
Funding
Open Access funding enabled and organized by Projekt DEAL. This work was funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation), grant number SFB 940, project C6.
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R.O. and H.K. conducted the data analysis, and RO wrote the manuscript text. T.E. designed the study and provided scripts for data analysis. R.O. organized data collection. T.E. and A.G.F. supervised data analysis. All authors contributed to interpretation and reviewed the manuscript.
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Overmeyer, R., Kirschner, H., Fischer, A.G. et al. Unraveling the influence of trial-based motivational changes on performance monitoring stages in a flanker task. Sci Rep 13, 19180 (2023). https://doi.org/10.1038/s41598-023-45526-0
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DOI: https://doi.org/10.1038/s41598-023-45526-0
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