Exogenous influences on task set activation in task switching

To explore the effect of exogenous processes on cognitive control, we used a cueing task-switching paradigm with two spatial judgement tasks and added an irrelevant colour attribute to the task-relevant spatial attribute of the target. The colour was not related to any specific Stimulus–Response relation in the tasks. A correlation was created between stimulus colour and task identity. This correlation was strong but imperfect in Experiment 1 and perfect in Experiment 2. As a result of the colour–task correlation, stimuli contained redundant information about task identity. By changing the correlation pattern every few blocks we caused this information to be sometimes invalid. In both experiments, performance was worse when the information carried by the target was invalid than when it was valid. However, this effect was exclusive to conditions with short task preparation time. By comparing performance with a control group, which had no colour–task correlation (in Experiment 2) we established that the colour manipulation did not cause a qualitative change in preparation strategy, and that the exogenous effect was stronger in switch trials than in repetition trials. We conclude that exogenous processes that are related to task set affect performance primarily if they are presented before endogenous processes of task set preparation have been launched.     

Task conflict effect in task switching

A part of action preparation is deciding what the relevant task is. This task-decision process is conceptually separate from response selection. To show this, the authors manipulated task conflict in a spatial task-switching paradigm, using conflict stimuli that appeared during trials with univalent targets (affording 1 task). The conflict stimuli afforded task identity because they were used as task cues with bivalent targets (affording 2 tasks) that were intermixed with the univalent targets. Thus, for univalent targets, irrelevant stimuli either caused low task conflict or high task conflict. In three experiments, the authors found poorer performance in high task conflict trials than in low task conflict trials. Task conflict was introduced during target appearance (Experiment 1) or task preparation (Experiments 2 and 3). In the latter case, the task conflict effect decreased with increasing task preparation time showing that task preparation involves task decision.     

Instruction effects in task switching

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.     

Spatial attention can be biased towards an expected dimension

A commonly held view in both exogenous and endogenous orienting is that spatial attention is associated with enhanced processing of all stimuli at the attended location. However, we often search for a specific target at a particular location, so an observer should be able to jointly specify the target identity and expected location. Whether attention can bias dimension-specific processes at a particular location is not yet clear. We used a dual task to examine the effects of endogenous spatial cues on the accuracy of perceptual judgments of different dimensions. Participants responded to a motion target and a colour target, presented at the same or different locations. We manipulated a central cue to predict the location of the motion or colour target. While overall performance in the two tasks was comparable, cueing effects were larger for the target whose location was predicted by the cue, implying that when attending a particular location, processing of the likely dimension was preferentially enhanced. Additionally, an asymmetry between the motion and colour tasks was seen; motion was modulated by attention, and colour was not. We conclude that attention has some ability to select a dimension at a particular location, indicating integration of spatial and feature-based attention.     

Novel n-back spatial working memory task using eye movement response

We created a novel eye movement version of the n-back task to measure spatial working memory (WM). Rather than one continuous trial, discrete trials were presented in order to develop a simpler WM task. In Experiment 1, we varied the visibility of the final stimulus to maximize the difference in performance between 0-back and 1-back tasks (WM effect). In Experiment 2, we administered the optimized task to children. In Experiment 3, we further simplified the task. Both adults and children easily completed our task, displaying significant WM effects. Further, similar WM effects were obtained in our original and simplified n-back spatial WM tasks, demonstrating flexibility. Because WM deficits are often an early feature of disease and a marker of disease progression, our saccadic measure of spatial WM may be particularly useful in hard-to-test populations, such as patients and children, and may have application in brain-imaging studies that require discrete trials.     

The effect of task location and task type on backward inhibition

Alternating tasks in a sequence of task switches results in impaired performance, relative to switches across three different tasks, an effect known as backward inhibition. Despite the robustness of this effect across task and response variations, backward inhibition is not observed when tasks are uniquely located at different points in space (Arbuthnott, 2005). Three hypotheses about the source of this anomaly were tested. Experiment 1 indicated that perceptually distinct task features other than location did not eliminate backward inhibition. Experiment 2 indicated that when switches across task and location were manipulated independently (i.e., all tasks appeared at all locations), backward inhibition was observed for task switches even when consecutive trials appeared at different spatial locations, ruling out eye movement as the source of the difference. The third experiment indicated that when component tasks involved judgments of spatial location, backward inhibition was observed across unique task-location switches. These results indicate that sequential inhibition is a very flexible mechanism that is sensitive to the amount of interference from previous tasks.     

Inhibition of return for the length of a line?

Inhibition of return is most often measured using an exogenous spatial cuing method. The experiments presented here follow up on a small number of studies that have examined whether a similar effect occurs for nonspatial stimulus attributes. In Experiments 1 and 2, the task was to identify a target line as either short or long. In this context, targets on valid trials were of the same length as that of a preceding cue, whereas targets on invalid trials were of a different length than that of a preceding cue. The results were similar to those in spatial orienting studies in that responses were slower for valid than for invalid targets only at stimulus onset asynchronies (SOAs) longer than 300 msec. In Experiment 3, the stimuli were the same but the task was to detect the onset of the target line. This task change resulted in slower responses for valid than for invalid targets at all SOAs. A similar result was observed in Experiment 4, in which validity was defined by color rather than line length, and the task was to identify the target color. The discussion centers on an opponent process approach to interpreting cuing effects, and consequent difficulties in distinguishing spatial and nonspatial cuing effects based on their time course.     

Current task activation predicts general effects of advance preparation in task switching

Two experiments investigated the way that beforehand preparation influences general task execution in reaction-time matching tasks. Response times (RTs) and error rates were measured for switching and nonswitching conditions in a color- and shape-matching task. The task blocks could repeat (task repetition) or alternate (task switch), and the preparation interval (PI) was manipulated within-subjects (Experiment 1) and between-subjects (Experiment 2). The study illustrated a comparable general task performance after a long PI for both experiments, within and between PI madipulations. After a short PI, however, the general task performance increased significantly for the between-subjects manipulation of the PI. Furthermore, both experiments demonstrated an analogous preparation effect for both task switching and task repetitions. Next, a consistent switch cost throughout the whole run of trials and a within-run slowing effect were observed in both experiments. Altogether, the present study implies that the effects of the advance preparation go beyond the first trials and confirms different points of the activation approach (Altmann, 2002) to task switching.     

Verbal representation in task order control: An examination with transition and task cues in random task switching

Recent task-switching studies in which a predictable task sequence has been used have indicated that verbal representation contributes to the control of task order information. The present study focused on the role of verbal representation in sequential task decisions, which are an important part of task order control, and examined the effects of articulatory suppression in a random-task-cuing paradigm with two different types of cues presented just before the presentation of a stimulus: a transition cue and a task cue. The former cue provided information only about switching or repeating the task, whereas the latter was associated directly with the identity of the task (i.e., indicating a parity or a magnitude task). In Experiment 1, in which transition cues guided task sequences, articulatory suppression impaired performance in both repetition and switch trials, thereby increasing the mixing costs. In Experiment 2, in which a task cue, rather than a transition cue, was presented to examine the influence of a cue-decoding process, articulatory suppression had no specific effect on task performance. Experiment 3, in which the transition cue and the task cue were randomly presented in the same block to equalize the memory load and task strategy for the two types of cues, confirmed that articulatory suppression significantly increased the mixing costs only in transition cue trials. The results from the three experiments indicated that the use of verbal representation is effective in sequential task decision—that is, in selecting a task set on the basis of transient task order information in both repetition and switch trials.     

Identity primes produce facilitation in a colour naming task

Five experiments examined associative or identity priming effects in a colour-naming task with colour-neutral words. In Experiment 1, subjects instructed to read the prime silently showed no associative priming effect but a colour-naming facilitation with identity priming. In Experiment 2, the typical associative priming interference in colour naming was demonstrated in subjects recalling the prime word, but not in subjects reading the prime silently, whereas associative primes facilitated word naming regardless of the prime response requirement. The remaining studies investigated the colour-naming facilitation observed with identity primes. Experiment 3 showed no effects on the facilitation of colour naming from varying the letter case of a silently read prime. Experiment 4 showed facilitation when subjects recalled the prime, and a target frequency effect, with faster colour-naming latencies for high- and medium- than low-frequency targets. In Experiment 5, there was no facilitation for naming the colour of target words paired with non-word primes differing in their initial letter from the target. Taken together, the results suggest that the facilitation of colour naming following identical primes reflects faster target word recognition, whereas the associative priming interference reflects an attentional effect.     

A secondary task is not always costly: Context‐based guidance of visual search survives interference from a demanding working memory task

Repeatedly encountering a visual search display with the target located at a fixed position relative to the distractors facilitates target detection, relative to novel displays – which is attributed to search guidance by (acquired) long‐term memory (LTM) of the distractor ‘context’ of the target. Previous research has shown that this ‘contextual cueing’ effect is severely impeded during learning when participants have to perform a demanding spatial working memory (WM) task concurrently with the search task, though it does become manifest when the WM task is removed. This has led to the proposal that search guidance by LT context memories critically depends on spatial WM to become ‘expressed’ in behaviour. On this background, this study, of two experiments, asked: (1) Would contextual cueing eventually emerge under dual‐task learning conditions if the practice on the task(s) is extended beyond the short training implemented in previous studies? and given sufficient practice, (2) Would performing the search under dual‐task conditions actually lead to an increased cueing effect compared to performing the visual search task alone? The answer is affirmative to both questions. In particular, Experiment 1 showed that a robust contextual cueing effect emerges within 360–720 dual‐task trials as compared to some 240 single‐task trials. Further, Experiment 2 showed that when dual‐ and single‐task conditions are performed in alternating trials blocks, the cueing effect for the very same set of repeated displays is significantly larger in dual‐task blocks than in single‐task blocks. This pattern of effects suggests that dual‐task practice eventually leads to direct, or ‘automatic’, guidance of visual search by learnt spatial LTM representations, bypassing WM processes. These processes are normally engaged in single‐task performance might actually interfere with direct LTM‐based search guidance.     

Dissociating restart cost and mixing cost in task switching

Three experiments investigated the cognitive mechanisms underlying the restart cost and mixing cost in task switching. To this aim, the predictability of task order was varied (unpredictable in Experiment 1 and predictable in Experiments 2 and 3) across experiments, which employed a multiple-trial paradigm. Verbal cues for color and shape matching tasks were presented before a run of four trials. Focusing on task-repetition runs only, we measured restart cost as the difference in performance between trials 1 and 2 and mixing cost as the difference in performance on the non-cued trials under mixed-tasks conditions (Experiments 1 and 2) and single-task conditions (Experiment 3). The restart cost was observed under mixed-tasks conditions with both unpredictable and predictable task orders but not under the single-task condition. In contrast, the mixing cost was observed under the mixed-tasks condition with unpredictable task order only (Experiment 1). This finding implies that the optimal task execution on repetition trials depends on how predictable the identity of the approaching task is. Therefore, we suggest that mixing cost arises from limited preparation on repetition trials when task order is unpredictable, while restart cost arises from processes involved in cue-based task activation that is needed to resolve task interference. Together, these data suggest that restart cost and mixing cost are based on dissociable mechanisms.

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Involuntary strategy-dependent dual task performance

Previous studies showed that some dual tasks can be performed simultaneously without costs. Yet, a variable SOA between the inputs to such tasks leads to strategic, often involuntary, prioritization of one of the two tasks. Here we explore the boundary conditions for this involuntary or exogenous strategy. In Experiment 1, subjects were initially trained on dual task performance where the input to the two tasks is presented simultaneously (0 SOA). We used two tasks that under such conditions can be performed without costs and indeed subjects displayed perfect sharing of the tasks. Subjects then performed the same two tasks but with a variable SOA (0, 50, 150, 800?ms). This manipulation led to a serial-like performance of the two tasks even in trials with 0 SOA. In Experiment 2, subjects participated in eight sessions. Within each session, they performed in alternation blocks with a fixed 0 SOA and blocks with a variable SOA. Subjects displayed perfect sharing in the pure 0 SOA blocks but performed the two tasks serially in the mixed SOA blocks despite receiving identical instructions. These findings demonstrate that task context is a powerful factor in dual task performance and may lead subjects to involuntarily exhibit dual task costs even in conditions where they can perform the tasks without any costs. Moreover, these findings strongly suggest that costs observed in PRP studies reflect the use of such exogenous strategies rather than a general structural dual task limitation.     

Exploring task-set reconfiguration with random task sequences

Switching between two different tasks normally results in an impairment in people's performance known as a switch cost, typically measured as an increase in reaction time (RT) and errors compared to a situation in which no task switch is required. Researchers in task switching have suggested that this switch cost is the behavioural manifestation of the task set reconfiguration processes that are necessary to perform the upcoming task. However, an examination of the literature in task switching reveals apparently contradictory results about the nature of task set reconfiguration processes. In Experiment 1, we addressed this issue by comparing participants' performance in two different experimental conditions: predictable task switching and random task switching. In the predictable switch condition the switch cost completely vanished after the first repetition of the new task. However, in the random switch condition, while the difference between switch and repetition trials was not significant, we observed a significant reduction in RT between the first and second repetition of the new task. In Experiment 2, we further investigated the pattern of task set reconfiguration in the random switch situation. The results showed a progressive reduction of participants' response latencies across repetitions of the same task. The present study demonstrates that, whereas the results in predictable switching conditions are compatible with an exogenous-reconfiguration hypothesis, random task switching produces a more gradual, decay-like switch cost reduction with task repetition.     

The costs of crossing paths and switching tasks between audition and vision

Switching from one functional or cognitive operation to another is thought to rely on executive/control processes. The efficacy of these processes may depend on the extent of overlap between neural circuitry mediating the different tasks; more effective task preparation (and by extension smaller switch costs) is achieved when this overlap is small. We investigated the performance costs associated with switching tasks and/or switching sensory modalities. Participants discriminated either the identity or spatial location of objects that were presented either visually or acoustically. Switch costs between tasks were significantly smaller when the sensory modality of the task switched versus when it repeated. This was the case irrespective of whether the pre-trial cue informed participants only of the upcoming task, but not sensory modality (Experiment 1) or whether the pre-trial cue was informative about both the upcoming task and sensory modality (Experiment 2). In addition, in both experiments switch costs between the senses were positively correlated when the sensory modality of the task repeated across trials and not when it switched. The collective evidence supports the independence of control processes mediating task switching and modality switching and also the hypothesis that switch costs reflect competitive interference between neural circuits.     

Congruency sequence effect in cross-task context: Evidence for dimension-specific modulation

The congruency sequence effect refers to a reduced congruency effect after incongruent trials relative to congruent trials. This modulation is thought to be, at least in part, due to the control mechanisms resolving conflict. The present study examined the nature of the control mechanisms by having participants perform two different tasks in an alternating way. When participants performed horizontal and vertical Simon tasks in Experiment 1A, and horizontal and vertical spatial Stroop task in Experiment 1B, no congruency sequence effect was obtained between the task congruencies. When the Simon task and spatial Stroop task were performed with different response sets in Experiment 2, no congruency sequence effect was obtained. However, in Experiment 3, in which the participants performed the horizontal Simon and spatial Stroop tasks with an identical response set, a significant congruency sequence effect was obtained between the task congruencies. In Experiment 4, no congruency sequence effect was obtained when participants performed two tasks having different task-irrelevant dimensions with the identical response set. The findings suggest inhibitory processing between the task-irrelevant dimension and response mode after conflict.     

The go/no-go priming task: automatic evaluation and categorisation beyond response interference

The response-window version of a go/no-go (GNG) response priming task is introduced using both evaluative (Experiment 1) and animacy decision (Experiment 2). In each trial a cue indicates which target category should lead to a key-press. The target is preceded by either a congruent or incongruent prime. The standard priming task was added as well. Both tasks yielded robust priming effects. However, they differed regarding a signature of response activation paradigms, that is, the Gratton effect (i.e. smaller priming effects following incongruent trials compared to congruent trials), which is present in the standard task but absent in the GNG task. This indicates that effects found with the GNG task are caused by different processes compared to the standard task. Experiment 3 tested an alternative account to explain priming effects in the GNG task. By manipulating response biases, Experiment 3 provides evidence for this account.     

No-go trials can modulate switch cost by interfering with effects of task preparation

It has recently been shown that the cost associated with switching tasks is eliminated following ‘no-go’ trials, in which response selection is not completed, suggesting that the switch cost depends on response selection. However, no-go trials may also affect switch costs by interfering with the effects of task preparation that precede response selection. To test this hypothesis we evaluated switch costs following standard go trials with those following two types of non-response trials: no-go trials, for which a stimulus is presented that indicates no response should be made (Experiment 1); and cue-only trials in which no stimulus is presented following the task cue (Experiment 2). We hypothesized that eliminating no-go stimuli would reveal effects of task preparation on the switch cost in cue-only trials. We found no switch cost following no-go trials (Experiment 1), but a reliable switch cost in cue-only trials (i.e., when no-go stimuli were removed; Experiment 2). We conclude that no-go trials can modulate the switch cost, independent of their effect on response selection, by interfering with task preparation, and that the effects of task preparation on switch cost are more directly assessed by cue-only trials.     

Task-set reconfiguration with predictable and unpredictable task switches

Participants switched frequently between high/low and odd/even classification of a digit. The interval between a task cue and the next digit varied between blocks. In Experiment 1, the task switched predictably every two, four, or eight trials. In Experiment 2, switching predictably every four trials was compared with random switching. With predictable switching, the cost was limited to the first trial of a run. Random switching produced a more gradual approach to asymptotic performance. After one performance, control processes attenuate the resulting change in task-set bias if a further switch is likely, but this strategic modulation is soon overwhelmed by task-set priming through further performances. Preparation reduced switch costs but not interference from the irrelevant attribute: Control of interference appears to be reactive, not proactive. Switch costs did not increase with run length, suggesting that retrieval of the task set last associated with the stimulus did not contribute to switch costs.     

Separate mechanisms recruited by exogenous and endogenous spatial cues: evidence from a spatial Stroop paradigm

The present experiments tested whether endogenous and exogenous cues produce separate effects on target processing. In Experiment 1, participants discriminated whether an arrow presented left or right of fixation pointed to the left or right. For 1 group, the arrow was preceded by a peripheral noninformative cue. For the other group, the arrow was preceded by a central, symbolic, informative cue. The 2 types of cues modulated the spatial Stroop effect in opposite ways, with endogenous cues producing larger spatial Stroop effects for valid trials and exogenous cues producing smaller spatial Stroop effects for valid trials. In Experiments 2A and 2B, the influence of peripheral noninformative and peripheral informative cues on the spatial Stroop effect was directly compared. The spatial Stroop effect was smaller for valid than for invalid trials for both types of cues. These results point to a distinction between the influence of central and peripheral attentional cues on performance and are not consistent with a unitary view of endogenous and exogenous attention.