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The prevalence of media multitasking - the concurrent use of multiple forms of media - has motivated research on whether and how it is related to various cognitive abilities, such as the ability to switch tasks. However, previous research on the relationship between media multitasking and task-switching performance has yielded mixed results, possibly because of small sample sizes and a confound between task and cue transitions that resulted in switch costs being impure measures of task-switching ability. The authors conducted a large-sample study in which media multitasking behavior was surveyed and task-switching performance was assessed using two cues per task, thereby allowing switch costs to be partitioned into task-switching and cue-repetition effects. The main finding was no evidence of any relationship between media multitasking scores and task-switching effects (or cue-repetition effects), either in correlational analyses or in extreme group analyses of light and heavy media multitaskers. The results are discussed in the context of previous research, with implications for studying media multitasking in relation to task-switching performance.

Conflict during response selection in task switching is indicated by the response congruency effect: worse performance for incongruent targets (requiring different responses across tasks) than for congruent targets (requiring the same response). The effect can be explained by dual-task processing in a mediated route for response selection, whereby targets are categorized with respect to both tasks. In the present study, the author tested predictions for the modulation of response congruency effects by categorization difficulty derived from a relative-speed-of-processing hypothesis. Categorization difficulty was manipulated for the relevant and irrelevant task dimensions in a novel spatial task-switching paradigm that involved judging the locations of target dots in a grid, without repetition of dot configurations. Response congruency effects were observed and they varied systematically with categorization difficulty (e.g., being larger when irrelevant categorization was easy than when it was hard). These results are consistent with the relative-speed-of-processing hypothesis and suggest that task-switching models that implement variations of the mediated route for response selection need to address the time course of categorization.

Hick’s law describes the increase in choice reaction time (RT) with the number of stimulus-response (S-R) mappings. However, in choice RT experiments, set-size is typically confounded with stimulus recency and frequency: With a smaller set-size, each stimulus occurs on average more frequently and more recently than with a larger set-size. To determine to what extent stimulus recency and frequency contribute to the set-size effect, stimulus set-size was manipulated independently of stimulus recency and frequency, by keeping recency and frequency constant for a subset of the stimuli. Although this substantially reduced the set-size effect (by approximately two-thirds for these stimuli), it did not eliminate it. Thus, the time required to retrieve an S-R mapping from memory is (at least in part) determined by the number of alternatives. In contrast, a recent task switching study (Van ‘t Wout et al. in Journal of Experimental Psychology: Learning, Memory & Cognition., 41, 363–376, 2015) using the same manipulation found that the time required to retrieve a task-set from memory is not influenced by the number of alternatives per se. Hence, this experiment further supports a distinction between two levels of representation in task-set control: The level of task-sets, and the level of S-R mappings.

Visual statistical learning (VSL), the unsupervised learning of statistical contingencies across time and space, may play a key role in efficient and predictive encoding of the perceptual world. How VSL capabilities vary as a function of ongoing task demands is still poorly understood. VSL is modulated by selective attention and faces interference from some secondary tasks, but there is little evidence that the types of contingencies learned in VSL are sensitive to task demands. We found a powerful effect of task on what is learned in VSL. Participants first completed a visual familiarization task requiring judgments of face gender (female/male) or scene location (interior/exterior). Statistical regularities were embedded between stimulus pairs. During a surprise recognition phase, participants showed less recognition for pairs that had required a change in response key (e.g., female followed by male) or task (e.g., female followed by indoor) during familiarization. When familiarization required detection of "flicker" or "jiggle" events unrelated to image content, there was weaker, but uniform, VSL across pair types. These results suggest that simple task manipulations play a strong role in modulating the distribution of learning over different pair combinations. Such variations may arise from task and response conflict or because the manner in which images are processed is altered.

The present study investigated whether the advanced reconfiguration processes of the voluntary switching (VTS) paradigm were different from those of the instructed task switching (ITS) paradigm by examining event-related potentials (ERPs) in a within-subjects design. Of importance, given that effector-to-task mapping might lead to differential preparatory strategies, two effector-to-task mapping groups were studied: the hand-to-task (HAND) and finger-to-task (FINGER) groups. Intriguingly, we found the increased posterior negativity for voluntary switch (and/or increased posterior positivity for voluntary repeat) was exclusive to the HAND group, whereas the increased switch-related late posterior positivity in the ITS paradigm was independent of the effector manipulation. Moreover, the lateralized readiness potentials (LRP) and the mu and beta motor-related amplitude asymmetries indicated that the differential switch-related modulations were not the byproduct of hand-specific preparation. The advanced preparatory strategies in the VTS and ITS paradigms are discussed.

Recent research has shown that objects near the hands receive preferential visual processing. However, it is not known whether proximity to the hands can affect executive functions. Here we show, using two popular paradigms, that people exhibit enhanced cognitive control for stimuli that are near their hands: We observed reduced interference from incongruent flankers in a visual attention task, and reduced costs when switching to an alternative task in a task-switching paradigm. The results reveal a remarkable influence of posture on cognitive function and have implications for assessing the potential benefits of working on handheld devices.

Ophir, Nass, and Wagner (Proceedings of the National Association of Sciences 106:15583-15587, 2009) reported that individuals who routinely engage in multiple forms of media use are actually worse at multitasking, possibly due to difficulties in ignoring irrelevant stimuli, from both external sources and internal representations in memory. Using the media multitasking index (MMI) developed by Ophir et al., we identified heavy media multitaskers (HMMs) and light media multitaskers (LMMs) and tested them on measures of attention, working memory, task switching, and fluid intelligence, as well as self-reported impulsivity and self-control. We found that people who reported engaging in heavy amounts of media multitasking reported being more impulsive and performed more poorly on measures of fluid intelligence than did those who did not frequently engage in media multitasking. However, we could find no evidence to support the contention that HMMs are worse in a multitasking situation such as task switching or that they show any deficits in dealing with irrelevant or distracting information, as compared with LMMs.

In the present study, we investigated how task selection is biased by inherent stimulus characteristics in the voluntary task-switching paradigm. We used digits as the task stimuli, since they may automatically induce spatially horizontal representations of numbers. Specifically, we examined whether an irrelevant spatial representation of a number coincides with its associated response codes and whether such a stimulus-response (S-R) correspondence effect biases task selection for a digit. Participants were randomly assigned to one of two different action code layout conditions: Two numerical tasks were arranged as inner/outer in the horizontal layout condition or as upper/down in the vertical layout condition. Participants in the horizontal layout condition were more likely to choose a task when the task's action code and the digit's spatial representation corresponded, as compared with when they did not. On the other hand, no selection bias was observed in the vertical layout condition, since there was no overlapping spatial representation between the stimulus and response. The present study extends previous findings by considering the influence of the stimulus-driven effect on task selection with regard to the S-R correspondence effect.

An increasing number of studies have demonstrated that a response in one task can be activated automatically on the basis merely of instructed stimulus-response (S-R) mappings belonging to another task. Such instruction-based response activations are considered to be evidence for the formation of S-R associations on the basis of the S-R mappings for an upcoming, but not yet executed, task. A crucial but somewhat neglected assumption is that instructed S-R associations are formed only under conditions that impose a sufficient degree of task preparation. Accordingly, in the present study we investigated the relation between task preparation and the instruction-based task-rule congruency effect, which is an index of response activation on the basis of instructions. The results from two experiments demonstrated that merely instructed S-R mappings of a particular task only elicit instruction-based response activations when that task is prepared for to a sufficient degree. Implications are discussed for the representation of instructed S-R mappings in working memory.

The roles of verbal short-term memory (vSTM) in task selection and task performance processes were examined when individuals were asked to voluntarily choose which of two tasks to perform on each trial randomly. Consistent with previous voluntary task-switching (VTS) research, we hypothesized that vSTM would support random task selection by maintaining a sequence of previously executed tasks that would be used by a representativeness heuristic. Furthermore, because using a representativeness heuristic requires sufficient time for updating and comparison processes, we expected that vSTM would have a greater effect on task selection when more time was available. Participants completed VTS under concurrent articulatory suppression and foot tapping at short and long response-to-stimulus intervals (RSIs). Task selection in VTS was more repetitive under suppression than under foot tapping, but this effect did not vary with RSI, suggesting that vSTM does not maintain the sequence of executed tasks to guide task selection. Instead, vSTM is critical for maintaining the intended task and ensuring that it is carried out. In contrast to the finding that a working memory load impairs task performance, we found no difference in reaction times and no switch costs between suppression and foot-tapping conditions, suggesting that vSTM is not critical for task performance.

Research suggests that regular aerobic exercise has the potential to improve executive functioning, even in healthy populations. The purpose of this review is to elucidate which components of executive functioning benefit from such exercise in healthy populations. In light of the developmental time course of executive functions, we consider separately children, young adults, and older adults. Data to date from studies of aging provide strong evidence of exercise-linked benefits related to task switching, selective attention, inhibition of prepotent responses, and working memory capacity; furthermore, cross-sectional fitness data suggest that working memory updating could potentially benefit as well. In young adults, working memory updating is the main executive function shown to benefit from regular exercise, but cross-sectional data further suggest that task-switching and post error performance may also benefit. In children, working memory capacity has been shown to benefit, and cross-sectional data suggest potential benefits for selective attention and inhibitory control. Although more research investigating exercise-related benefits for specific components of executive functioning is clearly needed in young adults and children, when considered across the age groups, ample evidence indicates that regular engagement in aerobic exercise can provide a simple means for healthy people to optimize a range of executive functions.

Although the concept of automaticity is closely associated with extensive rote training, previous studies have shown that task-defined stimulus-response (S-R) mappings can be implemented in parallel and involuntarily, without much training, as if they are automatically processed. An irrelevant task context may trigger a task-defined rule because the rule is actively maintained in working memory, resulting in erroneous implementation of that rule. However, the present study demonstrated that active maintenance of task rules is not necessary for their automatic implementation. Instead, the results are consistent with the memory view of automaticity, according to which task-defined S-R rules are implemented via automatic retrieval of S-R episodes.

Identification of the second of two targets (T1, T2, inserted in a stream of distractors) is impaired when presented within 500 ms after the first (attentional blink, AB). Barring a T1-T2 task-switch, it is thought that T2 must be backward-masked to obtain an AB (Giesbrecht & Di Lollo, Journal of Experimental Psychology: Human Perception and Performance, 24, 1454-1466, 1998). We tested the hypothesis that Giesbrecht & Di Lollo's findings were vitiated by ceiling constraints arising from either response scale (experiment 1) or data limitations (experiment 2). In experiment 1, digit-distractors were replaced with pseudoletters to increase task difficulty, bringing performance below ceiling. An AB occurred without backward masking of T2. In experiment 2, a ceiling-free procedure estimated the number of noise dots needed for 80% T2 identification. An AB was revealed: fewer noise dots were required during the AB period than outside it. Both outcomes confirm that an AB can be obtained without either masking of T2 or task switching.

A large component of response time switch costs in the cued task-switching paradigm is linked to cue changes without task changes, suggesting costs might reflect passive priming rather than endogenous control. In contrast, the task span procedure requires subjects to guide task selection via sequences of memorized task cues and therefore may be better suited to reflect endogenous switch processes (Logan, 2004). The present experiments combined the task span procedure with a 2:1 mapping between cues and tasks, allowing separation of cue-switch costs from true task-switch costs. Replicating findings with the cued task-switching paradigm, results showed both substantial cue-switch costs and actual task-switch costs (Experiments 1 and 2) as well as sensitivity of cue-switch costs, but not of task-switch costs, to opportunity for preparation (Experiment 2). Apparently, simple action plans use "surface level" phonological or articulatory codes that contain no task information. These results suggest that the distinction between cue-related and task-related processes is critical no matter whether tasks are cued exogenously or endogenously.

We tested the hypothesis that persisting activation from a previous task execution does not contribute to the switch cost in voluntary task switching. We reasoned that voluntary task switching requires the selection of random task sequences, which necessitates the active inhibition of previously executed tasks. The asymmetric switch cost was used as a marker for persisting activation. Participants switched voluntarily between color naming and word naming. One group was instructed to select unpredictable task sequences. The other group was not instructed to do so. When participants were instructed to be unpredictable, no asymmetric switch cost was observed. When participants were not instructed to be unpredictable, an asymmetric switch cost was observed. We conclude that the amount of persisting activation in voluntary task switching is limited and that the switch cost in voluntary task switching reflects the time needed for reconfiguring the cognitive system from one task to another rather than the time needed to compensate for persisting activation.

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-22 task-repetition costs, which currently constitute the most convincing evidence for inhibition of task sets. n-22 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. Author Note

This study looked for evidence of task-set inhibition in a voluntary task-switching paradigm. Participants performed one of three tasks on a digit: parity (even or odd), size (less than or greater than 5), or distance (near or far from 5). On each trial, they were allowed to choose which task to perform, with encouragement to perform each task equally often overall and in a random sequence. The question was whether participants would avoid performing a task that they had recently switched away from (e.g., the task performed on trial n-2), because the task set was still inhibited. Results confirmed that participants strongly avoided performing the n-2 task (e.g., ABA) in favor of performing other tasks (e.g., ABC). This occurred both when participants were required to switch tasks every trial (Experiment 1) and when they were allowed to repeat tasks (Experiment 2). The results suggest that a task set is inhibited during switching to a new task, reducing the likelihood that this task will be selected in the near future.

Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany The present study examined the effect of instructions on sequential task preparation using a cuing paradigm with three tasks. All task transitions were predictable, whereas task identity was unpredictable in switches but predictable in repetitions. In Experiment 1, predictability (predictable vs. random) was manipulated while preparation time (i.e., the cue-stimulus interval, or CSI) remained constantly short. In Experiment 2, CSI was manipulated for predictable task transitions. Both experiments showed clear instruction effects, but these were restricted to predictable task repetitions, for which predictability determined the identity of the upcoming task. Predictability effects were small in task switches and were not modulated by instruction, suggesting that preparation is mainly task-specific rather than switch-specific. Together, these results suggest that intentional processes contribute to predictability benefits in task repetitions, probably by enhancing the monitoring of sequential transitions in working memory in order to maintain activation in task repetitions.

The switch cost asymmetry (i.e., larger costs when switching from a nondominant into a dominant task than vice versa) has been explained in terms of the trial-to-trial carryover of activation levels required for the dominant versus the nondominant task. However, there is an open question about whether an actual switch in task is in fact necessary to obtain a "selection" cost asymmetry. In Experiments 1 and 2, we modified an alternating-runs paradigm to include either long or short response-to-stimulus intervals (RSIs) after each pair of trials (i.e., AA-AA-BB-BB), thereby inducing selection costs not only at the point of a task switch (i.e., AA-BB), but also between same-task pairs (i.e., AA-AA). Using spatially compatible versus incompatible response rules (Experiment 1) and Stroop word versus color naming (Experiment 2), we found asymmetric effects not only at task-change transitions, but also at task-repeat transitions when the RSI was long (presumably inducing frequent losses of set). In Experiments 3A and 3B, a cost asymmetry for long RSIs was obtained even when competing tasks were separated into alternating single task blocks, but not when the tasks were compared in a between-subjects design. This general pattern cannot be explained by activation carryover models, but is consistent with the idea that the asymmetry arises as a result of interference from long-term memory traces.

Children sometimes have trouble switching from one task to another, despite demonstrating an awareness of current task demands. This behavior could reflect problems either directly inhibiting previously relevant information or sufficiently activating graded working me mory representations forthe current task. We tested competing predictions from each account, using a computerized card-sorting task in which we assessed children's task switching abilities and their response speed to simple questions about current task demands. All children answered these questions correctly, but children who successfully switched tasks responded more quickly to questions than did children who perseverated on previous tasks, even after factoring out processing speed and age. This reaction time difference supports graded working memory accounts, with stronger representations of current task demands aiding both task-switching and responses to questions. This result poses a challenge for directed inhibition accounts, because nothing needs to be inhibited to answer simple questions that lack conflicting information.

Two converging tests were used to determine whether people proactively inhibit recently performed tasks when switching to new tasks. A task-cuing paradigm was used. In each trial, the relevant stimulus was accompanied by flankers belonging either to the task performed on the immediately preceding trial (lag 1) or a more distant trial (lag 2 +). If the just-performed task is inhibited when switching to another task, and this inhibition declines across trials, then flanker interference should be smaller with lag 1 flankers than with lag 2 + flankers. Experiment 1, following the methods of Hübner, Dreisbach, Haider, and Kluwe (2003), failed to confirm this prediction. The prediction was confirmed in Experiment 2, however, using a design modified to provide greater incentives for task-set inhibition. The results provide evidence that inhibition can be applied proactively, to reduce the ability of an abandoned task to interfere with the performance of other tasks.

Some researchers argue that task switching involves task-set reconfiguration-that is, changing the existing task set to perform a different task. Although this idea is intriguing, it is often unclear what is reconfigured and which processes are involved in reconfiguration. We addressed these issues by defining task sets, identifying differences between them, and obtaining evidence that was diagnostic of reconfiguration. In two experiments, subjects performed relative judgment tasks that involved comparing a target with a reference point that repeated or switched across trials. The task was the same on every trial, but the task set was not, because a task-set parameter-the reference point-had to be changed. Target-reference point distance effects that changed with the reference point provided diagnostic evidence that reconfiguration occurred, and this reconfiguration led to switch costs. We discuss how our approach can be generalized to define reconfiguration more clearly in other task-switching situations. nt|mis|This research was supported by Grants BCS 0133202 and BCS 0446806 from the National Science Foundation to G.D.L.

When an initial phase of cued task switching is followed by a phase of single-task trials, older adults show difficulties changing to the more efficient single-task mode of processing (Mayr & Liebscher, 2001). In Experiment 1, we show that these costs follow older adults’ continued tendency to inspect task cues even though these provide no new information. In Experiment 2, we included a condition in which task cues were eliminated from the display after the task-switching phase. In this condition, older adults behaved the same as younger adults, suggesting that the presence of the task cue is critical for observing age differences while switching from a “high-control” to a “low-control” mode of processing. We discuss our results in terms of a life-span shift with regard to the reliance on internal versus external sources of information under conditions of high-control demands.

Residual switch costs are notoriously difficult to eliminate. Yet Hunt and Klein (2002) eliminated them in a task that required observers to alternate between 8 trials of prosaccades and 8 trials of antisaccades, as long as there was at least 1 sec between the task cue and the onset of the saccade target. It was proposed that the elimination of residual switch costs occurred because prosaccade responses are computed very rapidly. These so-called hypercompatible responses bypass memory retrieval stages of the response process, thereby eliminating the source of residual switch costs. Here we tested this hypothesis by requiring observers to alternate between responding with the finger that was vibrated (another task that meets the criteria for hypercompatibility) and responding with the finger of the opposite hand. Residual switch costs were not eliminated, suggesting that their elimination in Hunt and Klein (2002) was due to special properties of the prosaccade-antisaccade task.

This study assessed whether or not the difficulty of task switching stems from previous inhibition of the task set. A predictable sequence of univalent stimuli (affording performance of one active task) and bivalent stimuli (affording performance of two tasks) was used in two experiments. Experiment 1 used an alternating-runs paradigm (AABB) and Experiment 2 used a strictly alternating sequence (ABAB). The critical variable was whether the incentive for task-set inhibition was strong (on bivalent trials) or weak (on univalent trials). The question was whether it would be more difficult to switch to a task that previously needed to be inhibited than to a task that did not need to be inhibited. This pattern was not observed in either experiment. Thus, the data provide no evidence that task switching is difficult because of the need to overcome recent task-set inhibition.

Inhibition of abandoned tasks in task switching can be inferred when a worse performance is found with n - 2 task repetitions (ABA sequences) than with nonrepetitions (CBA sequences). Recent evidence has shown that this inhibition effect decreases with long intertrial intervals (i.e., response-cue intervals, RCIs). Two alternatives have been proposed to account for this decrease. One alternative attributes the observed decrease to the decay of inhibition itself. The other alternative proposes that decay of the activation of competing tasks reduces the interference and leads to less inhibition. To decide between these alternatives, we manipulated RCI trialwise. The results favor the decay-of-activation account as an explanation for the decreased inhibition effect. This links the amount of inhibition to the activation level of the competing tasks, whereas evidence for the decay of inhibition remains weak.

In two experiments, subjects were given arbitrary letter cues or meaningful word cues that specified the task to be performed on a subsequent target stimulus. Letter and word cues were presented in separate blocks. There were two cues of each type for each task. Three kinds of transitions separated tasks: cue repetitions, in which both the cue and the task repeated; task repetitions, in which the cue changed but the task repeated; and task alternations, in which both the cue and the task changed. Responses were faster for cue than for task repetitions for both cue types. With word cues, task repetitions were not reliably faster than task alternations. With letter cues, task repetitions were reliably faster than task alternations in the first block but not in the second block. The results suggest that subjects responded to the compound of the cue and the target rather than switching task set between trials.