Task Repetition Costs Research Articles

Reward-based modulation of task-switching performance: a diffusion model analysis.

Investigating the interface between motivation and cognitive control, we conducted two task switching experiments (N = 96 each) with reward manipulation where participants switched between three different tasks. We measured N-2 task repetition costs, which denote the performance decrement in N-2 task repetition sequences (ABA) relative to N-2 task switch sequences (CBA), and which are presumed to be a marker of inhibitory control in task switching. Participants in the reward group received performance-contingent reward in the second phase of each experiment, and in the second experiment they were additionally penalized for errors. Reward thresholds were determined individually based on participants' performance during the first phase of each experiment. Participants in the control group did not receive any reward. The reward manipulation led to faster performance in the reward group relative to the control group. Diffusion modeling revealed that the reward manipulation induced an increase in drift rate parameter, consistent with dopamine-based enhancement of attentional focus under reward. Contrary to our expectations, no robust evidence for a reward-based modulation of N-2 repetition costs was found across the two experiments. N-2 task repetition costs were small in both experiments, and possibly, a larger amount of inhibitory control is needed in order to obtain empirical evidence for a reward-related modulation thereof. However, additional analyses suggested that reward may not interact with inhibitory control on the task level at all.

The impact of stimulus format on task inhibition during task switching.

Switching between competing tasks is supported by active inhibition of the preceding task. The level of task stimulus processing at which interference between competing tasks must occur for inhibition to be recruited is still unclear. Here, we investigated whether inhibition is recruited by task conflict occurring at an early or late (semantic) stage of task stimulus processing by dissociating the task stimulus format from its meaning. In two experiments, participants performed three different numerical judgment tasks on numerical stimuli that could be presented as digits or number words (e.g., "6" or "six") in a cued task-switching procedure. The effects of the change of stimulus format for the inhibition of the previous task were investigated and assessed by the N-2 task repetition cost, an index of the extent to which task representations are inhibited. The N-2 task repetition cost observed in the same stimulus format condition disappeared when target stimuli on task N-1 were presented in a different format from stimuli of task N-2 and N. This occurred both when the format changed from digits to number words stimuli (Experiment 1) as well as when it changed from number words to digits stimuli (Experiment 2). Results indicated that task set inhibition is recruited very early during the stimulus processing stage. They also provided evidence that task inhibition is not tied to task preparation processes but operates as a reactive, rather than proactive mechanism of conflict resolution.

On the reliability of behavioral measures of cognitive control: retest reliability of task-inhibition effect, task-preparation effect, Stroop-like interference, and conflict adaptation effect

This study examined the reliability (retest and split-half) of four common behavioral measures of cognitive control. In Experiment 1 (N = 96), we examined N – 2 task repetition costs as a marker of task-level inhibition, and the cue-stimulus interval (CSI) effect as a marker of time-based task preparation. In Experiment 2 (N = 48), we examined a Stroop-like face-name interference effect as a measure of distractor interference control, and the sequential congruency effect (“conflict adaptation effect”) as a measure of conflict-triggered adaptation of cognitive control. In both experiments, the measures were assessed in two sessions on the same day, separated by a 10 min-long unrelated filler task. We observed substantial experimental effects with medium to large effect sizes. At the same time, split-half reliabilities were moderate, and retest reliabilities were poor, for most measures, except for the CSI effect. Retest reliability of the Stroop-like effect was improved when considering only trials preceded by congruent trials. Together, the data suggest that these cognitive control measures are well suited for assessing group-level effects of cognitive control. Yet, except for the CSI effect, these measures do not seem suitable for reliably assessing interindividual differences in the strength of cognitive control, and therefore are not suited for correlational approaches. We discuss possible reasons for the discrepancy between robustness at the group level and reliability at the level of interindividual differences.

The effect of episodic retrieval on inhibition in task switching: a diffusion model analysis

Inhibition in task switching is inferred from n-2 task repetition costs: slower response times and poorer accuracy for ABA task switching sequences compared to CBA sequences, thought to reflect the persisting inhibition of task A across an ABA sequence. Much work has examined the locus of this inhibition effect, with evidence that inhibition targets response selection processes. Consistent with this, fits of the diffusion model to n-2 task repetition cost data have shown that the cost is reflected by lower estimates of drift rate, suggesting that inhibition impairs information processing efficiency during response selection. However, we have shown that the n-2 task repetition cost is confounded with episodic retrieval effects which masquerade as inhibitory costs. The purpose of the current study was to conduct a comprehensive analysis of diffusion model fits to new data within a paradigm that controls for episodic interference. Across four experiments (total N = 191), we find evidence that the reduction of drift rate for n-2 task repetition costs is only evident under conditions of episodic interference, and the cost is absent when this interference is controlled for. In addition, we also find evidence that episodic retrieval influences task preparation processes and response caution. These findings provide important constraints for theories of task switching that suggest inhibition selectively targets response selection processes.

The effect of practice on inhibition in task switching: Controlling for episodic retrieval

Previous work has shown that extended practice leads to a reduction in a key measure of cognitive inhibition during task switching: The n–2 task repetition cost. However, it has been demonstrated that this n–2 task repetition cost is increased by a non-inhibitory process—namely episodic retrieval—raising the question of whether the observed reduction of the cost with practice is driven by a reduction in inhibition, episodic retrieval effects, or a combination of both. The current study addresses this question by utilising a practice protocol using a task switching paradigm capable of controlling for episodic retrieval. The results showed a reduction in the n–2 task repetition cost with extended practice. The results also showed a clear increase of the n–2 task repetition cost due to episodic retrieval effects. The reduction of the cost with practice was driven by a reduction in inhibition and episodic retrieval contributions to the cost with practice, although there was a larger reduction in the episodic retrieval contribution with practice. The results are discussed with reference to current theoretical models of inhibition in task switching, which need to accommodate episodic retrieval and practice effects.

The effect of episodic retrieval on inhibition in task switching.

Inhibition in task switching is inferred from n-2 repetition costs: the observation that ABA task switching sequences are responded to slower than CBA sequences. This is thought to reflect the persisting inhibition of Task A, which slows reactivation attempts. Mayr (2002) reported an experiment testing a critical noninhibitory account of this effect, namely episodic retrieval: If the trial parameters for Task A match across an ABA sequence, responses should be facilitated because of priming from episodic retrieval; a cost would occur if trial parameters mismatch. In a rule-switching paradigm, Mayr reported no significant difference in n-2 repetition cost when the trial parameters repeated or switched across an ABA sequence, in clear contrast to the episodic retrieval account. What remains unclear is whether successful episodic retrieval modulates the n-2 repetition cost. Across 3 experiments-including a close replication of Mayr-we find clear evidence of reduced n-2 task repetition costs when episodic retrieval is controlled. We find that the effect of episodic retrieval on the n-2 task repetition cost is increased when the cue-task relationship is made more abstract, suggesting the effect is because of interference in establishing the relevant attentional set. We also demonstrate that the episodic retrieval effect is not influenced by retrieval of low-level, perceptual, elements. Together, the data suggest the n-2 task repetition cost-typically attributable to an inhibitory mechanism-also reflects episodic retrieval effects. (PsycINFO Database Record

Task Dominance Determines Backward Inhibition in Task Switching.

Switching between tasks is assumed to be accompanied by inhibiting currently irrelevant, but competing tasks. A dominant task that strongly interferes with performing a weaker task may receive especially strong inhibition. We tested this prediction by letting participants switch among three tasks that differ in dominance: a location discrimination task with strong stimulus–response bindings (responding with left-hand and right-hand button presses to stimuli presented left or right to the fixation cross) was combined with a color/pattern and a shape discrimination task, for which stimulus–response mappings were arbitrary (e.g., left-hand button press mapped to a red stimulus). Across three experiments, the dominance of the location task was documented by faster and more accurate responses than in the other tasks. This even held for incompatible stimulus–response mappings (i.e., right-hand response to a left-presented stimulus and vice versa), indicating that set-level compatibility (i.e., “dimension overlap”) was sufficient for making this location task dominant. As a behavioral marker for backward inhibition, we utilized n-2 repetition costs that are defined by higher reaction times for a switch back to a just abandoned and thus just inhibited task (ABA sequence) than for a switch to a less recently inhibited task (CBA, n-2 non-repetition). Reliable n-2 task repetition costs were obtained for all three tasks. Importantly, these costs were largest for the location task, suggesting that inhibition indeed was stronger for the dominant task. This finding adds to other evidence that the amount of inhibition is adjusted in a context-sensitive way.

Investigating task inhibition in children versus adults: A diffusion model analysis

One can take n−2 task repetition costs as a measure of inhibition on the level of task sets. When switching back to a Task A after only one intermediate trial (ABA task sequence), Task A is thought to still be inhibited, leading to performance costs relative to task sequences where switching back to Task A is preceded by at least two intermediary trials (CBA). The current study investigated differences in inhibitory ability between children and adults by comparing n−2 task repetition costs in children (9–11years of age, N=32) and young adults (21–30years of age, N=32). The mean reaction times and error rate differences between ABA and CBA sequences did not differ between the two age groups. However, diffusion model analysis revealed that different cognitive processes contribute to the inhibition effect in the two age groups: The adults, but not the children, showed a smaller drift rate in ABA than in CBA, suggesting that persisting task inhibition is associated with slower response selection in adults. In children, non-decision time was longer in ABA than in CBA, possibly reflecting longer task preparation in ABA than in CBA. In addition, Ex–Gaussian functions were fitted to the distributions of correct reaction times. In adults, the ABA–CBA difference was reflected in the exponential parameter of the distribution; in children, the ABA–CBA difference was found in the Gaussian mu parameter. Hence, Ex–Gaussian analysis, although noisier, was generally in line with diffusion model analysis. Taken together, the data suggest that the task inhibition effect found in mean performance is mediated by different cognitive processes in children versus adults.

Task Inhibition and Response Inhibition in Older vs. Younger Adults: A Diffusion Model Analysis.

Differences in inhibitory ability between older (64–79 years, N = 24) and younger adults (18–26 years, N = 24) were investigated using a diffusion model analysis. Participants performed a task-switching paradigm that allows assessing n−2 task repetition costs, reflecting inhibitory control on the level of tasks, as well as n−1 response-repetition costs, reflecting inhibitory control on the level of responses. N−2 task repetition costs were of similar size in both age groups. Diffusion model analysis revealed that for both younger and older adults, drift rate parameters were smaller in the inhibition condition relative to the control condition, consistent with the idea that persisting task inhibition slows down response selection. Moreover, there was preliminary evidence for task inhibition effects in threshold separation and non-decision time in the older, but not the younger adults, suggesting that older adults might apply different strategies when dealing with persisting task inhibition. N−1 response-repetition costs in mean RT were larger in older than younger adults, but in mean error rates tended to be larger in younger than older adults. Diffusion-model analysis revealed longer non-decision times in response repetitions than response switches in both age groups, consistent with the idea that motor processes take longer in response repetitions than response switches due to persisting response inhibition of a previously executed response. The data also revealed age-related differences in overall performance: Older adults responded more slowly and more accurately than young adults, which was reflected by a higher threshold separation parameter in diffusion model analysis. Moreover, older adults showed larger non-decision times and higher variability in non-decision time than young adults, possibly reflecting slower and more variable motor processes. In contrast, overall drift rate did not differ between older and younger adults. Taken together, diffusion model analysis revealed differences in overall performance between the age groups, as well as preliminary evidence for age differences in dealing with task inhibition, but no evidence for an inhibitory deficit in older age.

Analogous selection processes in declarative and procedural working memory: N-2 list-repetition and task-repetition costs

Working memory (WM) holds and manipulates representations for ongoing cognition. Oberauer (Psychology of Learning and Motivation, 51, 45-100, 2009) distinguishes between two analogous WM sub-systems: a declarative WM which handles the objects of thought, and a procedural WM which handles the representations of (cognitive) actions. Here, we assessed whether analogous effects are observed when participants switch between memory sets (declarative representations) and when they switch between task sets (procedural representations). One mechanism assumed to facilitate switching in procedural WM is the inhibition of previously used, but currently irrelevant task sets, as indexed by n-2 task-repetition costs (Mayr & Keele, Journal of Experimental Psychology: General, 129(1), 4-26, 2000). In this study we tested for an analogous effect in declarative WM. We assessed the evidence for n-2 list-repetition costs across eight experiments in which participants switched between memory lists to perform speeded classifications, mental arithmetic, or a local recognition test. N-2 list-repetition costs were obtained consistently in conditions assumed to increase interference between memory lists, and when lists formed chunks in long-term memory. Further analyses across experiments revealed a substantial contribution of episodic memory to n-2 list-repetition costs, thereby questioning the interpretation of n-2 repetition costs as reflecting inhibition. We reanalyzed the data of eight task-switching experiments, and observed that episodic memory also contributes to n-2 task-repetition costs. Taken together, these results show analogous processing principles in declarative and procedural WM, and question the relevance of inhibitory processes for efficient switching between mental sets.

The Effect of Episodic Retrieval on Inhibition in Task Switching

Inhibition in task switching is inferred from n-2 repetition costs: the observation that ABA task switching sequences are responded to slower than CBA sequences. This is thought to reflect the persisting inhibition of task A, which slows re-activation attempts. Mayr (2002) reported an experiment testing a critical non-inhibitory account of this effect, namely episodic retrieval: If the trial parameters for task A match across an ABA sequence, responses should be facilitated due to priming from episodic retrieval; a cost would occur if trial parameters mismatch. In a rule-switching paradigm, Mayr reported no significant difference in n-2 repetition cost when the trial parameters repeated or switched across an ABA sequence, in clear contrast to the episodic retrieval account. What remains unclear is whether successful episodic retrieval modulates the n-2 repetition cost. Across three experiments — including a close replication of Mayr (2002) — we find clear evidence of reduced n-2 task repetition costs when episodic retrieval is controlled. We find that the effect of episodic retrieval on the n-2 task repetition cost is increased when the cue–task relationship is made more abstract, suggesting the effect is due to interference in establishing the relevant attentional set. We also demonstrate that the episodic retrieval effect is not influenced by retrieval of low-level, perceptual, elements. Together, the data suggest the n-2 task repetition cost — typically attributable to an inhibitory mechanism — is largely explained by episodic retrieval effects.

The effect of N-3 on N-2 repetition costs in task switching.

N-2 task repetition cost is a response time and error cost returning to a task recently performed after one intervening trial (i.e., an ABA task sequence) compared with returning to a task not recently performed (i.e., a CBA task sequence). This cost is considered a robust measure of inhibitory control during task switching. The present article reports a novel sequential effect of n-2 task repetitions when trial n-3 is taken into consideration. In particular, performance is better in trials preceded by an n-2 repetition than in trials preceded by an n-2 switch. That is, performance is better in BABA sequences (where trial n-1 was an n-2 repetition) than in CABA sequences (where trial n-1 was an n-2 switch). Likewise, performance is better in BCBA (where trial n-1 was an n-2 repetition) than in ACBA or DCBA sequences (where trial n-1 was an n-2 switch). Evidence for this new n-3 effect is provided by a mini meta-analysis of a set of published data, as well as 2 new experiments applying a different paradigm. We suggest that this new effect reflects trial-by-trial modulation of cognitive control: Task conflict is higher in n-2 repetitions than in n-2 switches; therefore, cognitive control is increased in trials following n-2 repetitions, leading to improved performance. This facilitating effect of previous task conflict is discussed with respect to current theories on cognitive control.

Too much of a good thing: Stronger bilingual inhibition leads to larger lag-2 task repetition costs

Inhibitory control and monitoring abilities of Hebrew–English bilingual and English monolingual university students were compared, in a paradigm requiring participants to switch between performing three distinct tasks. Inhibitory control was gauged by lag-2 task repetition costs, namely decreased performance on the final trial of sequences of type ABA relative to CBA, due to persisting inhibition of the recently abandoned task. Bilinguals had larger lag-2 repetition costs, which reflect stronger inhibition of a no-longer relevant task to facilitate a switch into a new task. Monitoring ability was measured by the fadeout effect, which reflects adaptation to simpler task demands when a single task block immediately and unexpectedly follows mixed task blocks. Bilinguals did not differ from monolinguals in the magnitude or trajectory of the fade-out effect. Thus, results support the notion of increased bilingual inhibitory control, even when it is detrimental to performance, and do not demonstrate a specific bilingual advantage in monitoring. These findings are discussed in the context of the recent debate concerning the locus of bilingual advantages.

The role of task preparation and task inhibition in age-related task-switching deficits.

The aim of our study was to examine the role of task preparation and task inhibition in age-related task-switching deficits. In 2 experiments, we used a cuing paradigm with 3 tasks and manipulated the cue-stimulus interval (CSI). Additionally, switching among 3 tasks enabled us to examine n-2 task repetition costs, which reflect persisting inhibition of abandoned tasks. In Experiment 1, we found larger mixing costs (i.e., performance in mixed-task blocks vs. single-task blocks) in older adults than in young adults, and preparation effects were smaller in older adults than in young adults. In Experiment 2, where CSIs were blocked instead of randomly varied, we replicated reduced effects of task preparation in older adults. N-2 task repetition costs were not significant in Experiment 1 but significant in Experiment 2, and these costs did not differ across age groups in both experiments. The data suggest a task-preparation deficit in older adults that contributes to increased mixing costs in older adults.

Inhibitory Processes for Critical Situations – The Role of n−2 Task Repetition Costs in Human Multitasking Situations

The human cognitive system is equipped with various processes for dealing with everyday challenges. One of such processes is the inhibition of currently irrelevant goals or mental task-sets, which can be seen as a response to the critical event of information overflow in the cognitive system and challenging the cognitive system’s ability to keep track of ongoing demands. In two experiments, we investigate the flexibility of the inhibitory process by inserting rare non-critical events (25% of all trials), operationalized as univalent stimuli (i.e., unambiguous stimuli that call for only one specific task in a multitasking context), and by introducing the possibility to prepare for an upcoming task (Experiment 2). We found that the inhibitory process is not influenced by a cue informing subjects about the upcoming occurrence of a univalent stimulus. However, the introduction of univalent stimuli allowed preparatory processes to modify the impact of the inhibitory process. Therefore, our results suggest that inhibitory processes are engaged in a rather global manner, not taking into account variations in stimulus valence, which we took as operationalization of critical, conflict-inducing events in the ongoing stream of information processing. However, rare uncritical events, such as univalent stimuli that do not cause conflict and interference in the processing stream, appear to alter the way the cognitive system can take advantage of preparatory processes.

The role of inhibition in task switching: A review

The concept of inhibition plays a major role in cognitive psychology. In the present article, we review the evidence for the inhibition of task sets. In the first part, we critically discuss empirical findings of task inhibition from studies that applied variants of the task-switching methodology and argue that most of these findings-such as switch cost asymmetries-are ambiguous. In the second part, we focus on n-2 task-repetition costs, which currently constitute the most convincing evidence for inhibition of task sets. n-2 repetition costs refer to the performance impairment in sequences of the ABA type relative to CBA, which can be interpreted in terms of persisting inhibition of previously abandoned tasks. The available evidence suggests that inhibition is primarily triggered by conflict at selection of stimulus attributes and at the response level.

Control and interference in task switching—A review.

The task-switching paradigm offers enormous possibilities to study cognitive control as well as task interference. The current review provides an overview of recent research on both topics. First, we review different experimental approaches to task switching, such as comparing mixed-task blocks with single-task blocks, predictable task-switching and task-cuing paradigms, intermittent instructions, and voluntary task selection. In the 2nd part, we discuss findings on preparatory control mechanisms in task switching and theoretical accounts of task preparation. We consider preparation processes in two-stage models, consider preparation as an all-or-none process, address the question of whether preparation is switch-specific, reflect on preparation as interaction of cue encoding and memory retrieval, and discuss the impact of verbal mediation on preparation. In the 3rd part, we turn to interference phenomena in task switching. We consider proactive interference of tasks and inhibition of recently performed tasks indicated by asymmetrical switch costs and n-2 task-repetition costs. We discuss stimulus-based interference as a result of stimulus-based response activation and stimulus-based task activation, and response-based interference because of applying bivalent rather than univalent responses, response repetition effects, and carryover of response selection and execution. In the 4th and final part, we mention possible future research fields.

Dissociating cue-related and task-related processes in task inhibition: Evidence from using a 2:1 cue-to-task mapping.

Performance of task sequences is assumed to rely on activation and inhibition of tasks. An empirical marker of task inhibition is the so-called n-2 repetition cost, which is assessed by comparing performance in trial n-2 task repetitions (i.e., ABA) with that in n-2 task switches (i.e., CBA). Current theoretical accounts assume that inhibition acts on the level of task representations (i.e., task sets). However, another potential target of task inhibition could be the representation of the task cue. To decide between these two alternatives, the authors used a 2:1 cue-to-task mapping design. They found significant n-2 task repetition costs both with n-2 cue repetitions and n-2 cue switches. These costs were about equal (Experiment 1), and this data pattern was found for both short and long cuing intervals (Experiment 2). Together, the data suggest that task inhibition acts on task sets and not on cue representations.

The role of temporal cue-target overlap in backward inhibition under task switching

One of the proposed mechanisms for sequential control in task-shift conditions is backward inhibition (BI), which is usually measured in terms of lag-2 task repetition costs in A-B-A task sequences relative to C-B-A task sequences. By considering the so far existing experiments it seems that these lag-2 repetition costsoccur only with temporally overlapping cues and targets. In the present study this issue was further examined in two experiments, in which temporal cue-target overlap was varied blockwise (Experiment 1) and from trial-to-trial (Experiment 2). Experiment 1 shows that lag-2 repetition effects can only be observed with temporally overlapping cues and targets, indicating that there was no BI with temporally separated cues and targets. However, the results of Experiment 2 suggest that both irrelevant task sets are inhibited in this case, and that with temporally overlapping cues and targets only the previously relevant task set is inhibited.

The influence of overlapping response sets on task inhibition

The aim of the present study was to examine the contribution of overlapping response sets to the occurrence of task inhibition, measured as n-2 task repetition cost. We had subjects switch among four tasks. Three tasks overlapped on both stimulus set and response set. A fourth, neutral, univalent task never overlapped on the stimulus set but, across three experiments, varied in terms of the degree of overlap in the response set. We found that overlap in response set affects task inhibition. We suggest that response set overlap increases the competition among tasks and, thus, triggers task inhibition to resolve this competition.