Task coordination and aging: explorations of executive control processes in the task switching paradigm.

A number of models of cognitive aging suggest that older adults exhibit disproportionate performance decrements on tasks which require executive control processes. In a series of three studies we examined age-related differences in executive control processes and more specifically in the executive control processes which underlie performance in the task switching paradigm. Young and old adults were presented with rows of digits and were required to indicate whether the number of digits (element number task) or the value of the digits (digit value task) were greater than or less than five. Switch costs were assessed by subtracting the reaction times obtained on non-switch trials from trials following a task switch. Several theoretically interesting results were obtained. First, large age-related differences in switch costs were found early in practice. Second, and most surprising, after relatively modest amounts of practice old and young adults switch costs were equivalent. Older adults showed large practice effects on switch trials. Third, age-equivalent switch costs were maintained across a two month retention period. Finally, the main constraint on whether age equivalence was observed in task switching performance was memory load. Older adults were unable to capitalize on practice under high memory loads. These data are discussed in terms of their implications for both general and process specific cognitive aging models.     

The role of working memory capacity and interference resolution mechanisms in task switching

Theories of task switching have emphasized a number of control mechanisms that may support the ability to flexibly switch between tasks. The present study examined the extent to which individual differences in working memory (WM) capacity and two measures of interference resolution, response–distractor inhibition and resistance to proactive interference (PI), account for variability in task switching, including global costs, local costs, and N-2 repetition costs. A total of 102 young and 60 older adults were tested on a battery of tasks. Composite scores were created for WM capacity, response–distractor inhibition, and resistance to PI; shifting was indexed by rate residual scores, which combine response time and accuracy and account for individual differences in processing speed. Composite scores served as predictors of task switching. WM was significantly related to global switch costs. While resistance to PI and WM explained some variance in local costs, these effects did not reach significance. In contrast, none of the control measures explained variance in N-2 repetition costs. Furthermore, age effects were only evident for N-2 repetition costs, with older adults demonstrating larger costs than young adults. Results are discussed within the context of theoretical models of task switching.     

Inhibition in aging: What is preserved? What declines? A meta-analysis

Aging has been assumed to go along with deficient inhibitory processes in cognitive performance. According to this inhibition deficit hypothesis, older adults are less able to suppress or ignore irrelevant thoughts and actions than young adults are. This hypothesis has been investigated in a large number of studies. We conducted a meta-analysis to determine whether there is an inhibition deficit in older age and whether this deficit is general or task-specific. We selected 176 studies in which young and older adults were tested on tasks commonly assumed to measure inhibition (i.e., the color Stroop, flanker, Simon, stop-signal, go/no-go, global–local, positive and negative compatibility tasks, as well as the paradigm assessing n-2 repetition costs in task switching). For most tasks (i.e., the color Stroop, flanker, and local tasks, as well as the n-2 repetition costs), the results speak against an inhibition deficit in older age. Only in a few tasks (i.e., the go/no-go and stop-signal tasks), older adults showed impaired inhibition. Moreover, for four tasks (i.e., the Simon, global, positive and negative compatibility tasks), the results suggest that more studies are necessary to draw a firm conclusion. Together, the present findings call into question the hypothesis of a general inhibition deficit in older age.     

Age-related differences in switching between cognitive tasks: does internal control ability decline with age?

The present study tested the hypothesis that older adults establish a weaker task set than younger adults and therefore rely more on stimulus-triggered activation of task sets. This hypothesis predicts that older adults should have difficulty with task switches, especially when the stimuli-responses are associated with multiple, competing tasks. Weak task preparation, however, could actually benefit older adults when performing an unexpected task. The authors tested this prediction in Experiment 1 using a repeating AABB task sequence, with univalent and bivalent stimuli intermixed. On some univalent trials, participants received an unexpected task. Contrary to the authors' predictions, expectancy costs were not smaller for older adults. Similar findings were obtained in Experiments 2 and 3, in which the authors used a task-cueing paradigm to more strongly promote deliberate task preparation. The authors found no disproportionate age effects on switch costs but did find age effects on bivalence costs and mixing costs. The authors conclude that older adults do experience extra difficulty dealing with stimuli associated with 2 active tasks but found no evidence that the problem specifically stems from an increased reliance on bottom-up task activation rather than top-down task preparation.     

Changes in executive control across the life span: examination of task-switching performance

A study was conducted to examine changes in executive control processes over the life span. More specifically, changes in processes responsible for preparation and interference control that underlie the ability to flexibly alternate between two different tasks were examined. Individuals (N = 152) ranging in age from 7 to 82 years participated in the study. A U-shaped function was obtained for switch costs (i.e., the time required to switch between tasks compared with a repeated-task baseline), with larger costs found for young children and older adults. Switch costs were reduced with practice, particularly for children. All age groups benefited from increased preparation time, with larger benefits observed for children and older adults. Adults benefited to a greater extent than children when the interval between the response to one task and the cue indicating which task to perform next was lengthened, which suggested faster decay of interference from the old task set for adults than for children. A series of hierarchical analyses indicated that the age-related variance in task-switching performance is independent, at least in part, from the age-related variance in other cognitive processes such as perceptual speed and working memory. The results are discussed in terms of the development and decline of executive control processes across the life span.     

Ageing and switching of the focus of attention in working memory: results from a modified N-back task.

We conducted two experiments using a modified version of the N-Back task. For younger adults, there was an abrupt increase in reaction time of about 250 ms in passing from N = 1 to N > 1, indicating a cost associated with switching of the focus of attention within working memory. Response time costs remained constant over the range N = 2 to N = 5. Accuracy declined steadily over the full range of N (Experiment 1). Focus switch costs did not interact with either working memory updating (Experiment 1), or global task switching (Experiment 2). There were no age differences in RT costs once general slowing was taken into account, but there was a larger focus-switch-related accuracy cost in older adults than in younger adults. No age sensitivity was found for either updating or global task switching. The results suggest (a) that focus switching is a cognitive primitive, distinct from task switching and updating, and (b) that focus switching shows a specific age-related deficit in the accuracy domain.     

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.     

Age equivalence in switch costs for prosaccade and antisaccade tasks

This study examined age differences in task switching using prosaccade and antisaccade tasks. Significant specific and general switch costs were found for both young and old adults, suggesting the existence of 2 types of processes: those responsible for activation of the currently relevant task set and deactivation of the previously relevant task set and those responsible for maintaining more than 1 task active in working memory. Contrary to the findings of previous research, which used manual response tasks with arbitrary stimulus-response mappings to study task-switching performance, no age-related deficits in either type of switch costs were found. These data suggest age-related sparing of task-switching processes in situations in which memory load is low and stimulus-response mappings are well learned.     

The Role of Switching,Inhibition and Working Memory in Older Adults' Performance in the Wisconsin Card Sorting Test

ABSTRACT

The Wisconsin Card Sorting Test (WCST) is considered a typical executive test. However, several interesting questions are still open as to the specific executive processes underlying this task. In the present study, we explored how local and global switching, inhibition and working memory, assessed through the Number–Letter, the Stop Signal and the Reading Span tasks, relate to older adults' performance in the WCST. Results showed that older adults' performance variability in the number of perseverative errors was predicted by the local switch component of the Number–Letter task. Results also showed age-related differences in inhibition, working memory and global switching, while local switching resulted largely spared in aging. This study provides evidence that switching abilities may contribute to performance of older adults in the WCST. It also provides initial evidence suggesting that switching processes, associated with local switch costs, are involved in performance on the WCST, at least in older adults.     

Aging and auditory temporal sequencing: ordering the elements of repeating tone patterns

In a series of experiments, we examined age-related differences in adults' ability to order sequences of tones presented at various speeds and in contexts designed to promote or to impede stream segregation. In Experiment 1, 32 listeners (16 young, 16 old) were required to identify two repeating sequences that consisted of four tones (two from a high and two from a low frequency range) in different order. In Experiment 2, 32 listeners were required to judge whether the two recycled patterns from Experiment 1 were the same or different. In Experiment 3, four young and four old listeners were tested on the tasks of Experiment 2 over an extended period. In Experiment 4, 16 young and 16 old listeners were tested with sequences that were not recycled and were composed of tones drawn from a narrow frequency range. Elderly adults were less able than young adults to distinguish between tone sequences with contrasting order, regardless of the speed of presentation, the nature of the task (identification vs. same/different), the amount of practice, the frequency separation of the tones, or the presence or absence of recycling. These findings provide evidence of a temporal sequencing impairment in elderly listeners but reveal no indication of age differences in streaming processes.     

Hierarchical forms processing in adults and children

Two experiments examined child and adult processing of hierarchical stimuli composed of geometric forms. Adults (ages 18-23 years) and children (ages 7-10 years) performed a forced-choice task gauging similarity between visual stimuli consisting of large geometric objects (global level) composed of small geometric objects (local level). The stimuli spatial arrangement was manipulated to assess child and adult reaction times and predisposition toward local or global form categorization under two distinct trial conditions, with varied density of the local forms comprising the global forms. In Experiment 1, children and adults were presented with common, simple geometric shape hierarchical forms composed of ovals and rectangles. In Experiment 2, adults were presented with hierarchical forms composed of the simple geometric shapes, ovals and rectangles, and additional novel complex geometric shapes, “posts” and “arches.” Results show a clear increase of global processing bias across the age ranges of the individuals in the study, with children at 10 years performing similarly to adults on the simple stimuli. In addition, adults presented with the novel complex geometric shapes showed a significant reduction in global processing bias, indicating that form novelty and complexity lead to additional attention to local features in categorization tasks.     

Task switching and the measurement of “switch costs”

The measurement of “switch costs” is held to be of interest because, as is widely believed, they may reflect the control processes that are engaged when subjects switch between two (or more) competing tasks. [In task-switching experiments, the reaction time (RT) switch cost is typically measured as the difference in RT between switch and non-switch (repeat) trials.] In this report we focus on the RT switch costs that remain even after the subject has had some time to prepare for the shift of task, when the switch cost may be approximately asymptotic (so-called residual switch costs). Three experiments are presented. All three experiments used Stroop colour/word, and neutral stimuli. Participants performed the two tasks of word-reading and colour-naming in a regular, double alternation, using the “alternating runs” paradigm (R. D. Rogers & S. Monsell, 1995). The experiments were designed to test the hypothesis that RT switch costs depend on a form of proactive interference (PI) arising from the performance of a prior, competing task. A. Allport, E. A. Styles and S. Hsieh (1994) suggested that these PI effects resulted from “task-set inertia”, that is, the persisting activation-suppression of competing task-sets, or competing task-processing pathways. The results confirmed the existence of long-lasting PI from the competing task as a major contributor to switch costs. Non-switch trials, used as the baseline in the measurement of switch costs, were also shown to be strongly affected by similar PI effects. However, task-set inertia was not sufficient to account for these results. The results appeared inconsistent also with all other previous models of task switching. A new hypothesis to explain these between-task interference effects was developed, based on the stimulus-triggered retrieval of competing stimulus-response (S-R) associations, acquired (or strengthened) in earlier trials. Consistent with this retrieval hypothesis, switch costs were shown to depend primarily on the S-R characteristics of the preceding task (the task that was switched from) rather than the upcoming task. Further, the effects of the other, competing task were found to persist over many successive switching trials, affecting switch costs long after the stimulus overlap (and hence the principal S-R competition) between the current tasks had been removed. Switch costs were also found to be affected by recent, item-specific experience with a given stimulus, in either the same or the competing task. Finally, the results showed that switch costs were massively affected by the ratio of the number of prior trials, in response to the same stimuli, that had implemented either the currently intended or the competing S-R mappings. None of these effects are predicted by current models of residual switch costs, which appeal to the differences in control processes assumed to be engaged in switch versus non-switch trials. Received: 31 March 1999 / Accepted: 23 July 1999     

Maintaining readiness for mental rotation interferes with perceptual processes in children but with response selection in adults

Previous work revealed that mental rotation is not purely inserted into a same-different discrimination task. Instead, response time (RT) is slowed to upright stimuli in blocks containing rotated stimuli compared to RT to the same upright stimuli in pure upright blocks. This interference effect is a result of maintaining readiness for mental rotation. In two experiments we investigated previous evidence that these costs depend upon distinct sub-processes for children and for adults. In Experiment 1, the maintaining costs turned out to be independent of the visual quality of the stimulus for adults but not so for children. Experiment 2 revealed that the maintaining costs were greatly reduced for adults when they performed mental rotation as a go-no-go task, but not so for children. Taken together, both experiments provide evidence that whereas perceptual processes seem to be important for school-age children to maintain readiness for mental rotation, response selection is relevant for adults.     

Removing irrelevant information from working memory: a cognitive aging study with the modified Sternberg task

Two experiments with a modified Sternberg recognition task explored the ability of young and old adults to remove irrelevant information from working memory. The task involved 2 memory sets, 1 of which was later cued as irrelevant. The recognition probe was presented at a variable time after the cue. Two indicators of inhibition, the setsize effect of the irrelevant set and the reaction time cost of intrusion probes (i.e., negative probes present in the irrelevant list), were dissociated. Irrelevant setsize effects lasted less than 1 s after the cue and did not differ between old and young adults. Intrusion costs lasted up to 5 s and were disproportionally large for old adults. With the additional requirement to remember both lists until after the probe, young adults' intrusion costs in Experiment 2 were equivalent to those of old adults in Experiment 1, but the setsize effects of the irrelevant set was larger. The results are compatible with a dual-process model of recognition in combination with a working-memory model distinguishing the focus of attention from the activated portion of long-term memory.     

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.     

Age-related differences in reaction time task performance in young children

Performance of reaction time (RT) tasks was investigated in young children and adults to test the hypothesis that age-related differences in processing speed supersede a “global” mechanism and are a function of specific differences in task demands and processing requirements. The sample consisted of 54 4-year-olds, 53 5-year-olds, 59 6-year-olds, and 35 adults from Russia. Using the regression approach pioneered by Brinley and the transformation method proposed by Madden and colleagues and Ridderinkhoff and van der Molen, age-related differences in processing speed differed among RT tasks with varying demands. In particular, RTs differed between children and adults on tasks that required response suppression, discrimination of color or spatial orientation, reversal of contingencies of previously learned stimulus-response rules, and greater stimulus-response complexity. Relative costs of these RT task differences were larger than predicted by the global difference hypothesis except for response suppression. Among young children, age-related differences larger than predicted by the global difference hypothesis were evident when tasks required color or spatial orientation discrimination and stimulus-response rule complexity, but not for response suppression or reversal of stimulus-response contingencies. Process-specific, age-related differences in processing speed that support heterochronicity of brain development during childhood were revealed.     

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.     

Effects of auditory stimulus intensity on response force in simple, go/no-go, and choice RT tasks

In four experiments, increasing the intensities of both relevant and irrelevant auditory stimuli was found to increase response force (RF) in simple, go/no-go, and choice reaction time (RT) tasks. These results raise problems for models that localize the effects of auditory intensity on purely perceptual processes, indicating instead that intensity also affects motor output processes under many circumstances. In Experiment 1, simple RT, go/no-go, and choice RT tasks were compared, using the same stimuli for all tasks. Auditory stimulus intensity affected both RT and RF, and these effects were not modulated by task. In Experiments 2-4, an irrelevant auditory accessory stimulus accompanied a relevant visual stimulus, and the go/no-go and choice tasks were used. The intensity of the irrelevant auditory accessory stimulus was found to affect RT and RF, although the sizes of these effects depended somewhat on the temporal predictability of the accessory stimulus.     

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.     

Task switches under Go/NoGo conditions and the decomposition of switch costs

Alternating switches between two simple S-R tasks are combined with Go/NoGo tasks. Non-switches after Go trials are assumed to selectively profit from stimulus driven repetition benefits, whereas switches after NoGo trials are assumed to be selectively delayed by stimulus driven negative priming. Intentionally driven reconfiguration costs are assessed by RT differences between switches after Go trials (no negative priming) and non-switches after NoGo trials (no repetition benefits). Experiment 1 indicates that with short preparation time repetition benefits, negative priming costs, and intentional components contribute approximately additively to switch costs. Experiment 2 confirms that the delay of switches after NoGo trials is indeed due to negative priming. Experiments 3 and 4 show that repetition benefits and intentional components of switch costs are properly assessed only if the settings assure that participants reconfigure the required task set in NoGo as well as Go trials.