Switching between tasks and responses: a developmental study

Task switching requires the ability to flexibly switch between task rules and responses, and is sensitive to developmental change. We tested the hypothesis that developmental changes in task switch performance are associated with changes in the facilitating or interfering effect of the previously retrieved stimulus-response (S-R) association. Three age groups (7-8-year-olds, 10-12-year-olds and 20-25-year-olds) performed a two-choice reaction time (RT) task in which spatially compatible or incompatible responses were required. The RT costs associated with switching between tasks were larger when responses were repeated than when responses were alternated. Younger children showed a greater cost than adults when switching between tasks but repeating responses. This age difference decreased when the interval between the previous response and the upcoming stimulus increased. Switch costs were larger when switching to the compatible task than to the incompatible task, but this effect did not differ between age groups. These findings suggest that young children build up stronger transient associations between task sets and response sets, which interfere with their ability to switch to currently intended actions. A similar pattern has previously been observed for older adults (Mayr, 2001), suggesting a common contributor to task switching deficits across the life span.     

Response inhibition under task switching: its strength depends on the amount of task-irrelevant response activation

Under task switch conditions, response repetitions usually produce benefits if the task also repeats, but costs if the task switches. So far, it is largely undecided how to account for these effects. In the present study, we provide additional evidence in favor of the account that each response is inhibited in order to prevent its accidental re-execution. To test this hypothesis, the risk of an accidental re-execution of a given response was manipulated by modulating the activation of the response in the previous task. In Experiment 1, this was done by means of congruent and incongruent stimuli. As expected, on task switch trials, the repetition costs were larger if a congruent rather than an incongruent stimulus occurred in the previous task. In Experiment 2, the same effect occurred for stimulus-response compatible versus incompatible stimuli in the previous task. In Experiment 3, both manipulations were applied together, which produced almost additive effects. Altogether, the results support the inhibition account for the response repetition effects under task switch conditions.     

Eye movements, not hypercompatible mappings, are critical for eliminating the cost of task set reconfiguration

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-calledhypercompatible 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.     

Coactivation in the perception of redundant targets

Reaction time (RT) to redundant stimuli was investigated while controlling for distraction effects and response competition. In Experiment 1, a redundancy gain was found for 2 target letters with identical features (redundant) compared to trials in which 2 different targets shared the same response assignment (compatible) indicating coactivation of stimulus inputs. No difference in RTs was found between compatible displays and displays containing 2 targets with different responses (incompatible), suggesting (with other evidence) that letters were serially processed. In Experiment 2, a redundancy gain was again found. Unlike in Experiment 1, incompatible displays produced response competition, indicating a redundancy gain with parallel processing. Three forms of redundancy gains operating under specific conditions are discussed.     

An action sequence held in memory can interfere with response selection of a target stimulus,but does not interfere with response activation of noise stimuli

Withholding an action plan in memory for later execution can delay execution of another action if the actions share a similar (compatible) action feature (e.g., response hand). We investigated whether this phenomenon, termed compatibility interference (CI), occurs for responses associated with a target as well as responses associated with distractors in a visual selection task. Participants planned and withheld a sequence of keypress responses (with their right or left hand), according to the identity of a stimulus (A), and then immediately executed a keypress response (with their right or left hand) to a second stimulus (B), according to the identity of a target letter appearing alone or among distractor letters. Distractor letters were either response compatible or incompatible with the target and appeared either simultaneously with the target (Experiments 1A and 2) or 100 msec before the target (Experiment 1B). Also, stimulus-response mapping was either 1:1 (Experiment 1) or 2:1 (Experiment 2). Results showed that the response to the Stimulus B target was delayed when it required the same response hand as Stimulus A, as opposed to a different hand. Also, the target reaction time for Stimulus B was greater when the target was flanked by incompatible distractors than when it was flanked by compatible distractors. Moreover, the degree of CI was consistent across the compatible-, incompatible-, and no-distractor conditions, indicating that CI generalizes to responses associated with a target, but not to those associated with distractors. Thus, CI occurs at a response selection, not at a response activation stage. Implications for the code occupation account for CI (e.g., Stoet & Hommel, 1999, 2002) and an alternative account for CI are discussed.     

Mixing compatible and incompatible mappings: Elimination, reduction, and enhancement of spatial compatibility effects

In two-choice tasks, the compatible mapping of left stimulus to left response and right stimulus to right response typically yields better performance than does the incompatible mapping. Nonetheless, when compatible and incompatible mappings are mixed within a block of trials, the spatial compatibility effect is eliminated. Two experiments evaluated whether the elimination of compatibility effects by mixing compatible and incompatible mappings is a general or specific phenomenon. Left-right physical locations, arrow directions, and location words were mapped to keypress responses in Experiment 1 and vocal responses in Experiment 2. With keypresses, mixing compatible and incompatible mappings eliminated the compatibility effect for physical locations and arrow directions, but enhanced it for words. With vocal responses, mixing significantly reduced the compatibility effect only for words. Overall, the mixing effects suggest that elimination or reduction of compatibility effects occurs primarily when the stimulus-response sets have both conceptual and perceptual similarity. This elimination may be due to suppression of a direct response-selection route, but to account for the full pattern of mixing effects it is also necessary to consider changes in an indirect response-selection route and the temporal activation properties of different stimulus-response sets.     

Age differences in response selection for pure and mixed stimulus-response mappings and tasks

Two experiments examined effects of mixed stimulus-response mappings and tasks for older and younger adults. In Experiment 1, participants performed two-choice spatial reaction tasks with blocks of pure and mixed compatible and incompatible mappings. In Experiment 2, a compatible or incompatible mapping was mixed with a Simon task for which the mapping of stimulus color to location was relevant and stimulus location was irrelevant. In both experiments, older adults showed larger mixing costs than younger adults and larger compatibility effects, with the differences particularly pronounced in Experiment 1 when location mappings were mixed. In mixed conditions, when stimulus location was relevant, older adults benefited more than younger adults from complete repetition of the task and stimulus from the preceding trial. When stimulus location was irrelevant, the benefit of complete repetition did not differ reliably between age groups. The results suggest that the age-related deficit associated with mixing mappings and tasks is primarily due to older adults having more difficulty separating task sets that activate conflicting response codes.     

Task selection cost asymmetry without task switching

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 alternatingruns 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 betweensubjects 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.     

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.     

The role of sensory-motor modality compatibility in language processing

Language processing requires the combination of compatible (auditory-vocal and visual-manual) or incompatible (auditory-manual and visual-vocal) sensory-motor modalities, and switching between these sensory-motor modality combinations is very common in every-day life. Sensory-motor modality compatibility is defined as the similarity of stimulus modality and the modality of response-related sensory consequences. We investigated the influence of sensory-motor modality compatibility during performing language-related cognitive operations on different linguistic levels. More specifically, we used a variant of the task-switching paradigm, in which participants had to switch between compatible or between incompatible sensory-motor modality combinations during a verbal semantic categorization (Experiment 1) or during a word-form decision (Experiment 2). The data show higher switch costs (i.e., higher reaction times and error rates in switch trials compared to repetition trials) in incompatible sensory-motor modality combinations than in compatible sensory-motor modality combinations. This was true for every language-related cognitive operation, regardless of the individual linguistic level. Taken together, the present study demonstrates that sensory-motor modality compatibility plays an important role in modality switching during language processing.     

Effects of associative learning on age differences in task-set switching

Costs of switching between tasks may disappear when subjects are able to learn associations between tasks, stimuli, and responses (cf. Rogers, R. D., & Monsell, S. (1995). Costs of a predictable switch between simple cognitive tasks. Journal of Experimental Psychology: General, 124, 207-231). The first aim of this study was to examine this possibility by manipulating stimulus-set size. We expected that costs of switching between tasks would be strongly reduced under conditions of small stimulus-set sizes (n=4) as compared to large stimulus-set sizes (n=96) with increasing time on task. The second aim was to determine whether younger as well as older adults were able to create associations between task components. As age differences in task switching are often found to be larger when response mappings are incompatible we also investigated interactions with response compatibility. Results of our study indicated that practice effects on switch costs were much more pronounced for small than large stimulus-set sizes, consistent with the view that the strength of associations between task components facilitates task switching. Furthermore, we found that practice benefits on task switching for small stimulus-set sizes were sensitive to age and response compatibility. In contrast to younger adults, who showed a reduction of switch costs for both response mapping conditions, older adults showed a reduction of switch costs only when response mappings were compatible. That is, older adults showed less associative learning when the currently irrelevant task feature had to be suppressed, supporting the view that older adults have primarily problems in separating overlapping task-set representations.     

Individual differences in multiple types of shifting attention

Many researchers consider costs in shifting attention and mental set to reflect a basic ability to use top-down goal information to guide action. Although switch costs have been used as measures of individuals' executive function, whether common abilities underlie task set switching across different types of shifting tasks has not been well studied. In 249 participants, we studied whether switch costs in a novel two-choice reaction time task were correlated across variations in two variables: thelocus of representation (stimuli were either perceptually available or stored in working memory [WM]) and which of two judgment tasks was performed. Switch costs were asymmetrical, in that it was easier to switch to the easier judgment, and were related to overall and relative processing speed: Switch costs were higher when the task was more difficult. These factors should be accounted for when one is measuring individual differences in switch costs. After controlling for these effects, we found evidence for a common ability underlying switch costs that involved both task set preparation and response selection; however, residual shift costs, which involve only response selection, were uncorrelated across tasks. Correlations among switch costs were substantially higher within task type (e.g., correlations of WM shifting tasks with other WM shifting tasks and of perceptual tasks with perceptual ones), suggesting that there are also processes unique to switching within WM and switching among visible stimuli.     

Age Influences on Multi-Dimensional Set Switching

Using a task switching paradigm, we investigated age effects on switch costs as a function of the number of sets to be switched. In Experiment 1, younger and older subjects determined a color or shape of an object presented on the computer screen, responding either by moving the joystick or by pressing a button on the joystick. The switch costs were assessed with differences between switch trials (task-set switch, response-set switch, and double switch) and non-switch trials. Contrary to the prediction that age would negatively influence performance on the double switch trials, age effects on switch costs were observed only for the single switch trials (i.e., response-set switch condition). Additionally, both younger and older adults were capable of preparing for task and response-set switches in parallel. In Experiment 2, we manipulated the time available to prepare for a task and response-set switch. Both younger and older adults were able to utilize extra time to reduce switch costs. Furthermore, the age deficit found in Experiment 1 for response-set switching was eliminated in the second experiment in which preparation for task and response-set switching was temporally decoupled. The data are discussed in terms of task component coordination across the adult lifespan.     

The role of response selection for inhibition of task sets in task shifting

Response selection in task shifting was explored using a go/no-go methodology. The no-go signal occurred unpredictably with stimulus onset so that all trials required task preparation but only go trials required response selection. Experiment 1 showed that shift costs were absent after no-go trials, indicating that response processes are crucial for shift costs. In Experiment 2, backward inhibition was absent after no-go trials. Experiments 3 and 4 demonstrated that response selection, rather than execution, causes backward inhibition. All 4 experiments showed effects of preparation time in go trials, suggesting that advance preparation must have also occurred in no-go trials. The authors concluded that inhibition of irrelevant task sets arises only at response selection and that residual shift costs reflect such persisting inhibition.     

The role of response selection in sequence learning

We investigated the role of response selection in sequence learning in the serial reaction time (SRT) task, by manipulating stimulus–response compatibility. Under conditions in which other types of learning, like perceptual, response-based, and response-effect learning, were unaffected, sequence learning was better with an incompatible than with a compatible stimulus–response mapping. Stimulus discriminability, on the other hand, had no influence on the amount of sequence learning. This indicates that the compatibility effects cannot be accounted for by a different level of task difficulty. Relating our results to the dimensional overlap model (Kornblum, Hasbroucq, & Osman, 1990), which assumes that incompatible stimulus–response mappings require more controlled response selection than do compatible stimulus–response mapping, we suggest that sequence learning in the SRT task is particularly effective when response selection occurs in a controlled way.     

The role of input–output modality compatibility in task switching

Input–output (I–O) modality compatibility refers to the similarity of stimulus modality and modality of response-related sensory consequences. A previous study found higher switch costs in task switching in I–O modality incompatible tasks (auditory-manual and visual-vocal) than in I–O modality compatible tasks (auditory-vocal and visual-manual). However, these tasks had spatially compatible S–R mappings, which implied dimensional overlap (DO). DO may have led to automatic activation of the corresponding compatible responses in the incorrect response modality, thus increasing interference effects. The present study was aimed to examine the influence of DO on I–O modality compatibility effects. In two experiments, we found that I–O modality compatibility affects task switching even in tasks without DO, which even tended to result in further increased modality influences. This finding suggests that I–O modality mappings affect response selection by affecting between-task cross-talk not on the level of specific response codes but on the level of modality-specific processing pathways.     

Out with the old, in with the new: More valid measures of switch cost and retrieval time in the task span procedure

Two experiments provided new measures of switch cost and retrieval time in the task span procedure. In Experiment 1, subjects were given lists of six task names to remember, followed by six targets on which to perform the tasks named in the list. The lists contained alternations and repetitions, and switch costs were estimated by comparing reaction time (RT) on alternation and repetition trials. The experiment also included memory span and single task conditions, so switch costs could be estimated by subtracting the sum of the RT in those conditions from the task span RT, as in the original report (Logan, 2004). The data suggested that the original measure of switch cost was invalid and that the new measure was preferable. In Experiment 2, subjects performed each task on the list twice. Retrieval was required on the first but not on the second trial in each pair. Retrieval time was estimated by comparing the RT on trials that required retrieval with trials that did not require retrieval. This measure was more valid than the RT in the memory span condition of Experiment 1, which was used in the original report.     

What it costs to implement a plan: Plan-level and task-level contributions to switch costs

Four experiments were conducted to identify the costs of implementing a plan in the task span procedure, which requires subjects to retrieve the task to perform on the current target from a list of planned tasks in memory. Experiment 1 compared switch costs in the task span procedure with switch costs in the explicit task-cuing procedure, which presented cues indicating the task to perform on each target. Switch costs were greater in the task span procedure. Experiments 2-4 were designed to identify the sources of this difference. Experiment 2 showed that the requirement of establishing a correspondence between the list of task names and the list of targets contributed to switch costs. Experiment 3 showed that retaining lists of similar task names produced greater switch costs than did retaining lists of dissimilar task names. Experiment 4 showed that memory load had no effect on switch costs. The results are discussed in terms of the interaction between plan-level and task-level processing in the implementation of plans.     

Sequential effects on speeded information processing: a developmental study

Two experiments were performed to assess age-related changes in sequential effects on choice reaction time (RT). Sequential effects portray the influence of previous trials on the RT to the current stimulus. In Experiment 1, three age groups (7-9, 10-12, and 18-25 years) performed a spatially compatible choice task, with response-to-stimulus intervals (RSIs) of 50 and 500 ms varied between trial blocks. In Experiment 2, three age groups (7-9, 15-16, and 18-25 years) performed the task with spatial stimulus-response (S-R) mappings (compatible versus incompatible) varied between participants. For adults, the experiments yielded a pattern of sequential effects suggestive of "automatic facilitation" (i.e., a first-order repetition effect and a higher order benefit-only pattern for short RSIs) and "subjective expectancy" (i.e., a first-order alternation effect and a higher order cost-benefit pattern for long RSIs). Automatic facilitation was more pronounced for incompatible responses than for compatible responses. Both experiments showed the anticipated decrease in automatic facilitation with advancing age. Finally, the first-order alternation effect showed the predicted age-related increase, but the cost-benefit pattern revealed an opposite trend, suggesting that the first-order and higher order indexes of subjective expectancy may relate to dissociable mechanisms.     

The role of response selection in sequence learning

We investigated the role of response selection in sequence learning in the serial reaction time (SRT) task, by manipulating stimulus-response compatibility. Under conditions in which other types of learning, like perceptual, response-based, and response-effect learning, were unaffected, sequence learning was better with an incompatible than with a compatible stimulus-response mapping. Stimulus discriminability, on the other hand, had no influence on the amount of sequence learning. This indicates that the compatibility effects cannot be accounted for by a different level of task difficulty. Relating our results to the dimensional overlap model (Kornblum, Hasbroucq, & Osman, 1990), which assumes that incompatible stimulus-response mappings require more controlled response selection than do compatible stimulus-response mapping, we suggest that sequence learning in the SRT task is particularly effective when response selection occurs in a controlled way.