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.     

Does scene context always facilitate retrieval of visual object representations?

An object-to-scene binding hypothesis maintains that visual object representations are stored as part of a larger scene representation or scene context, and that scene context facilitates retrieval of object representations (see, e.g., Hollingworth, Journal of Experimental Psychology: Learning, Memory and Cognition, 32, 58-69, 2006). Support for this hypothesis comes from data using an intentional memory task. In the present study, we examined whether scene context always facilitates retrieval of visual object representations. In two experiments, we investigated whether the scene context facilitates retrieval of object representations, using a new paradigm in which a memory task is appended to a repeated-flicker change detection task. Results indicated that in normal scene viewing, in which many simultaneous objects appear, scene context facilitation of the retrieval of object representations-henceforth termed object-to-scene binding-occurred only when the observer was required to retain much information for a task (i.e., an intentional memory task).     

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.     

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 task rules and stimulus–response mappings in the task switching paradigm

Switch costs occur whenever participants are asked to switch between two or more task sets. In a typical task switching experiment, participants have to switch between two task sets composed of up to four different stimuli per task set. These 2 (task sets) x 4 (stimuli) contain only 8 different stimulus-response (S-R) mappings, and the question is why participants base their task performance on task sets instead of S-R mappings. The current experiments compared task performance based on task rules with performance based on single stimulus-response mappings. Participants were led to learn eight different S-R mappings with or without fore-knowledge about two underlying task sets. Without task set information no difference between shifts and repetitions occurred, whereas introducing task sets at the beginning led to significant switch costs. Most importantly, introducing task sets in the middle of the experiment also resulted in significant switch costs. Furthermore, introducing task rules at the beginning of the experiment lead to slower RTs when simple stimuli (Experiment 1) had to be processed. This detrimental effect disappeared with more complex stimuli (Experiment 2). Results will be discussed with respect to cognitive control.     

Exploring temporal dissipation of attention settings in auditory task switching

Using a cued auditory task-switching variant of dichotic listening, we varied the response–cue interval (RCI) to examine temporal dissipation effects. On each trial, participants were presented with two different number words, one spoken by a female speaker and another by a male speaker (dichotic listening), that served as competing targets for a numerical judgment. The gender of the task-relevant speaker was indicated by a visual task cue prior to each trial. Experiment 1A used two different cues for each task (i.e., gender) and showed only small cue repetition benefits (same cue vs. alternate cue) but large auditory switch costs (alternate cue vs. task switch). A replication without immediate cue repetitions (Experiment 1B) showed very similar switch costs, suggesting that immediate cue repetitions play a negligible role for the size of auditory task switch costs. Moreover, switch costs were reduced when the (entirely task-irrelevant) location of the task-relevant speaker changed, relative to when it was unchanged, suggesting an episodic feature-binding component in our dichotic-listening task. Importantly, both experiments showed no effect of RCI on auditory switch costs. Because statistical power for this null effect was reasonably high across experiments (n?=?50), this finding suggests that auditory attention settings do not dissipate quickly over time.     

Eliminating the cost of task set reconfiguration

With insufficient time to fully prepare for a switch in task, a deterioration in performance on the first trial of a new task would be expected. The interest of researchers has been captured by the residual switch costs that, surprisingly, remain despite sufficient time to prepare. We used avery simple task to investigate the costs to reaction time and accuracy associated with changing between two different instructional sets every eight trials. Subjects responded to left and right visual targets by making either spatially compatible or incompatible eye movements (Experiment 1) or buttonpress responses (Experiment 2). The subjects were cued as to whether to make the compatible or the incompatible response by the color of a border appearing on the perimeter of the display. In cases in which the subject alternated between making pro- and antisaccades, the large costs to reaction time and accuracy at the short cue-target stimulus onset asynchrony were completely eliminated when sufficient time was provided to prepare for the switch. This complete elimination of residual switch costs was not obtained when the same alternation was applied to manual responses. This pattern of results links residual costs to response selection processes and suggests that they are not a necessary component of the switch process. We propose that the elimination of "stubborn" residual switch costs is rooted in our use of a hypercompatible task (making saccades toward targets) that places minimal demands on response selection.     

Differential effects of cue changes and task changes on task-set selection costs

A task-switching paradigm with a 2:1 mapping between cues and tasks was used to separate cue-switching processes (indexed through pure cue-switch costs) from actual task-switching processes (indexed through additional costs in case of cue and task changes). A large portion of total switch costs was due to cue changes (Experiments 1 and 2), and cue-switch costs but not task-switch costs were sensitive to effects of practice (Experiment 1) and preparation (Experiment 2). In contrast, task-switch costs were particularly sensitive to response-priming effects (Experiments 1 and 2) and task-set inhibition (Experiment 3). Results suggest two processing stages relevant during task-set selection: cue-driven retrieval of task rules from long-term memory and the automatic application of rules to a particular stimulus situation.     

Response selection difficulty and asymmetrical costs of switching between tasks and stimuli: no evidence for an exogenous component of task-set reconfiguration

Four task-switching experiments examined the notion of an exogenous component of task-set reconfiguration (i.e., a process needed to shift task set that is not initiated in the absence of a task-associated figuration stimulus). The authors varied the complexity and familiarity of stimulus-response (SR) mapping rules to produce differentially time-consuming reconfiguration demands. Tasks with more complex or less familiar rules did not display increased switch costs, given that stimulus repetitions were excluded from the analysis. These results do not support the idea of exogenous reconfiguration. Moreover, stimulus repetitions inflated task-switch costs and did so disproportionately for tasks with increased response selection difficulty, thereby demonstrating that insufficient control of the sequence of stimuli may yield results that mimic those predicted by exogenous reconfiguration accounts.     

Positive affect facilitates task switching in the dimensional change card sort task: Implications for the shifting aspect of executive function

Using the modified Dimensional Change Card Sort task, we examined the influence of positive affect on task switching by inspecting various markers for the costs, including restart cost, switch cost and mixing cost. Given that the executive-control processes that underlie switching performance—i.e., inhibition or shifting—are distinct from the component processes that underlie non-switching performance—i.e., stimulus evaluation, resource allocation or response execution—we hypothesised that if positive affect facilitates task switching via executive-control processes, rather than via component processes, positive affect would reduce both switch and restart costs, but not mixing cost, because both switch and restart costs rely on executive processes, while mixing cost imposes only minimal demands on executive processes. We found beneficial effects of positive affect on both restart and switch costs, but not on mixing costs. These results suggest that positive affect improves switching abilities via executive processes rather than via component processes.     

Intentional attention switching in dichotic listening: Exploring the efficiency of nonspatial and spatial selection

Using an auditory variant of task switching, we examined the ability to intentionally switch attention in a dichotic-listening task. In our study, participants responded selectively to one of two simultaneously presented auditory number words (spoken by a female and a male, one for each ear) by categorizing its numerical magnitude. The mapping of gender (female vs. male) and ear (left vs. right) was unpredictable. The to-be-attended feature for gender or ear, respectively, was indicated by a visual selection cue prior to auditory stimulus onset. In Experiment 1, explicitly cued switches of the relevant feature dimension (e.g., from gender to ear) and switches of the relevant feature within a dimension (e.g., from male to female) occurred in an unpredictable manner. We found large performance costs when the relevant feature switched, but switches of the relevant feature dimension incurred only small additional costs. The feature-switch costs were larger in ear-relevant than in gender-relevant trials. In Experiment 2, we replicated these findings using a simplified design (i.e., only within-dimension switches with blocked dimensions). In Experiment 3, we examined preparation effects by manipulating the cueing interval and found a preparation benefit only when ear was cued. Together, our data suggest that the large part of attentional switch costs arises from reconfiguration at the level of relevant auditory features (e.g., left vs. right) rather than feature dimensions (ear vs. gender). Additionally, our findings suggest that ear-based target selection benefits more from preparation time (i.e., time to direct attention to one ear) than gender-based target selection.     

Effects of varying presentation time on long-term recognition memory for scenes: Verbatim and gist representations

Konkle, Brady, Alvarez and Oliva (Psychological Science, 21, 1551–1556, 2010) showed that participants have an exceptional long-term memory (LTM) for photographs of scenes. We examined to what extent participants’ exceptional LTM for scenes is determined by presentation time during encoding. In addition, at retrieval, we varied the nature of the lures in a forced-choice recognition task so that they resembled the target in gist (i.e., global or categorical) information, but were distinct in verbatim information (e.g., an “old” beach scene and a similar “new” beach scene; exemplar condition) or vice versa (e.g., a beach scene and a new scene from a novel category; novel condition). In Experiment 1, half of the list of scenes was presented for 1 s, whereas the other half was presented for 4 s. We found lower performance for shorter study presentation time in the exemplar test condition and similar performance for both study presentation times in the novel test condition. In Experiment 2, participants showed similar performance in an exemplar test for which the lure was of a different category but a category that was used at study. In Experiment 3, when presentation time was lowered to 500 ms, recognition accuracy was reduced in both novel and exemplar test conditions. A less detailed memorial representation of the studied scene containing more gist (i.e., meaning) than verbatim (i.e., surface or perceptual details) information is retrieved from LTM after a short compared to a long study presentation time. We conclude that our findings support fuzzy-trace theory.     

The role of semantic memory in short-term recall: effect of strategic retrieval ability in an elderly population

The present paper examines the relationship between two classic phenomena: semantic effects in short-term recall (STR) tasks, which are interpreted as indicating the involvement of long-term memory (LTM) in the functioning of short-term memory, on the one hand, and the existence of individual differences amongst elderly people in strategic retrieval ability (i.e., the ability to activate representations in LTM in a controlled way) on the other hand. Forty elderly participants completed a STR task under four different conditions which were thought to differentially involve LTM representations. Several executive functions, among which the strategic retrieval ability, were evaluated. The results showed that the participants who obtained the best performances in terms of strategic retrieval ability, and only in this executive ability, also exhibited better performances in the STR task, in particular when this task was performed under conditions which favored the use of LTM.     

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.     

Task- and location-switching effects on visual attention

In two experiments, we examined the effects of task and location switching on the accuracy of reporting target characters in an attentional blink (AB) paradigm. Single-character streams were presented at a rate of 100 msec per character in Experiment 1, and successive pairs of characters on either side of fixation were presented in Experiment 2. On each trial, two targets appeared that were either white letters or black digits embedded in a stream of black letter distractors, and they were separated by between zero and five items in the stream (lags 1-6). Experiment 1 showed that report of the first target was least accurate if it immediately preceded the second target and if the two targets were either both letters or both digits (task repetition cost). Report of the second target was least accurate if one or two distractors intervened between the two targets (the U-shaped AB lag effect) and if one target was a letter and the other a digit (task switch cost). Experiment 2 added location uncertainty as a factor and showed similar effects as Experiment 1, with one exception. Lag 1 sparing (the preserved accuracy in reporting the second of two targets if the second immediately follows the first) was completely eliminated when the task required attention switching across locations. Two-way additive effects were found between task switching and location switching in the AB paradigm. These results suggests separate loci for their attentional effects. It is likely that the AB deficit is due mainly to central memory limitations, whereas location-switching costs occur at early visual levels. Task-switching costs occur at an intermediate visual level, since the present task switch involved encoding differences without changes in stimulus-response mapping rules (i.e., the task was character identification for both letters and digits).     

任务切换理论争议新证据

任务切换是研究认知控制的主要范式之一。大量研究发现切换试次比重复试次的反应时更长,错误率更高,这种差异称为切换代价。任务切换时所产生切换代价的理论解释主要有惯性论、重构论和联结论。近十年来,这些理论均获得新的实验支持和发展,但其争议依旧,没有哪一理论能成功解释任务切换的所有效应。未来研究可以建立整合模型,以准确描述切换代价产生的认知机制。     

Sticky rules: integration between abstract rules and specific actions

The authors manipulated repetitions and/or changes of abstract response rules and the specific stimulus- response (S-R) associations used under these rules. Experiments 1 and 2, assessing trial-to-trial priming effects, showed that repetition of complete S-R couplings produced only benefits when the rule also repeated (i.e., rule-S-R conjunctions) but costs when identical S-R couplings repeated while rules changed. In Experiments 3 and 4, the authors manipulated amount of experience with specific rule-S-R conjunctions and demonstrated integration between rules and S-R couplings in terms of cumulative practice effects. However, unlike short-term priming effects, cumulative practice supported generalization of experience with specific S-R couplings across rule boundaries (Experiment 4). Results are discussed in terms of constraints on models of hierarchical control and in terms of qualitatively different ways in which people profit from very recent experiences (i.e., all-or-none access to working memory representations) versus cumulative experience (i.e., similarity-based retrieval from long-term memory).     

Stimulus–response bindings contribute to item switch costs in working memory

In counter updating tasks, responses are typically faster when items repeat than when they change (item switch costs). The present study explored the contribution of stimulus–response bindings to these item switch costs. In two experiments, we orthogonally manipulated the repetition/switch of to-be-counted items and the repetition/switch of required manual responses. Item switch costs were considerably lower when item switches were accompanied by response switches than when accompanied by response repetitions. Experiment 2 showed that, although there was also a smaller contribution from stimulus–stimulus bindings (i.e., shape-location), the major part was due to stimulus-response bindings. These results show that in the widely used standard version of the counter updating task, a considerable portion of item switch costs is caused by the unbinding of stimulus–response bindings rather than by processes of switching items in working memory.     

The effects of levels-of-processing and organization on conceptual implicit memory in the category exemplar production test

The distinction between item-specific and relational information (Hunt & Einstein, 1981) may be relevant to accounts of conceptual priming in the category exemplar production task. In three experiments, the implications of this hypothesis were tested by examining the effects of organization and levels-of-processing (LOP) on this implicit test. Consistent with the hypothesis, the effects of LOP were greater when study lists were organized by category than when they were presented randomly. Furthermore, when subjects claiming test awareness or intentional retrieval were excluded from the analysis, the LOP effect was reduced (and, in fact, eliminated) in the random list condition but remained robust in the categorized condition. Finally, the experimental design of the LOP manipulation (i.e., mixed-list within, blocked-list within, or between subjects) did not moderate the effects of LOP on this priming task.     

Planning paths to multiple targets: memory involvement and planning heuristics in spatial problem solving

For large numbers of targets, path planning is a complex and computationally expensive task. Humans, however, usually solve such tasks quickly and efficiently. We present experiments studying human path planning performance and the cognitive processes and heuristics involved. Twenty-five places were arranged on a regular grid in a large room. Participants were repeatedly asked to solve traveling salesman problems (TSP), i.e., to find the shortest closed loop connecting a start location with multiple target locations. In Experiment 1, we tested whether humans employed the nearest neighbor (NN) strategy when solving the TSP. Results showed that subjects outperform the NN-strategy, suggesting that it is not sufficient to explain human route planning behavior. As a second possible strategy we tested a hierarchical planning heuristic in Experiment 2, demonstrating that participants first plan a coarse route on the region level that is refined during navigation. To test for the relevance of spatial working memory (SWM) and spatial long-term memory (LTM) for planning performance and the planning heuristics applied, we varied the memory demands between conditions in Experiment 2. In one condition the target locations were directly marked, such that no memory was required; a second condition required participants to memorize the target locations during path planning (SWM); in a third condition, additionally, the locations of targets had to retrieved from LTM (SWM and LTM). Results showed that navigation performance decreased with increasing memory demands while the dependence on the hierarchical planning heuristic increased.