Task switching is often considered for evaluating limitations of cognitive flexibility. Switch costs are behavioural indices of limited cognitive flexibility, and switch costs may be decomposable into stimulus-and response-related fractions, as conjectured by the domain hypothesis of cognitive flexibility. According to the domain hypothesis, there exist separable stimulus-and response-related neural networks for cognitive flexibility, which should be discernible as distinct event-related potentials (ERPs). The present card-matching study allowed isolating stimulus-and response-related switch costs, while measuring ERPs evoked by task cues and target stimuli with a focus on the target-locked N2/P3 complex. Behavioural data revealed that both stimulus-task and response-task bindings contribute to switch costs. Cue-locked ERPs yielded larger anterior negativity/posterior positivity in response to switch cues compared to repeat cues. Target-locked ERPs revealed separable ERP correlates of stimulusand response-related switch costs. P3 waveforms with fronto-central scalp distributions emerged as a corollary of stimulus-related switch costs. Fronto-centrally distributed N2 waveforms occurred when stimulus-task and response-task bindings contributed jointly to switch costs. The reported N2/P3 ERP data are commensurate with the domain hypothesis according to which there exist separable stimulusand response-related neural networks for cognitive flexibility. A better understanding of the cognitive and neural mechanisms of executive control remains a major problem for cognitive neuroscience. Executive control may be defined as maintaining behavioural goal-directedness when irrelevant information exerts a potentially interfering impact 1,2. One source of interference may stem from slowly decaying representations of previously executed cognitive tasks 3. The persistence of these representations may impose limitations on cognitive flexibility, a major facet of executive control, which refers to the ability to switch smoothly back and forth between different cognitive tasks 4,5. Cognitive flexibility is often studied in task-switching paradigms (for overview see 6-8). In task-switching paradigms, the primary index for limitations of cognitive flexibility is switch costs 7,8. Switch costs are usually reflected in increases in response times (RTs) and/or error rates for switch trials relative to repeat trials. On switch trials, the demanded cognitive task differs from previously executed tasks, whereas on repeat trials, the previously demanded task can simply be re-executed. One core finding is that switch costs are reduced when task cues and target stimuli are presented sufficiently long periods of time apart, rendering proactive task preparation possible to some degree 9. However, residual switch costs remain even when cue-target intervals are very long. The occurrence of residual switch costs has been attributed to the need for reactive reconfiguration of task sets following target onset, which is due to the incompleteness of p...
This study aimed to test two common explanations for the general finding of age-related changes in the performance of timing tasks within the millisecond-to-second range intervals. The first explanation is that older adults have a real difficulty in temporal processing as compared to younger adults. The second explanation is that older adults perform poorly on timing tasks because of their reduced cognitive control functions. These explanations have been mostly contrasted in explicit timing tasks that overtly require participants to process interval durations. Fewer studies have instead focused on implicit timing tasks, where no explicit instructions to process time are provided. Moreover, the investigation of both explicit and implicit timing in older adults has been restricted so far to healthy older participants. Here, a large sample (N = 85) comprising not only healthy but also pathological older adults completed explicit (time bisection) and implicit (foreperiod) timing tasks within a single session. Participants’ age and cognitive decline, measured with the Mini-Mental State Examination (MMSE), were used as continuous variables to explain performance on explicit and implicit timing tasks. Results for the explicit timing task showed a flatter psychometric curve with increasing age or decreasing MMSE scores, pointing to a deficit at the level of cognitive control functions rather than of temporal processing. By contrast, for the implicit timing task, a decrease in the MMSE scores was associated with a reduced foreperiod effect, an index of implicit time processing. Overall, these findings extend previous studies on explicit and implicit timing in healthy aged samples by dissociating between age and cognitive decline (in the normal-to-pathological continuum) in older adults.
The spatial Stroop task measures the ability to resolve interference between relevant and irrelevant spatial information. We recently proposed a four-choice spatial Stroop task that ensures methodological advantages over the original color-word verbal Stroop task, requiring participants to indicate the direction of an arrow while ignoring its position in one of the screen corners. However, its peripheral spatial arrangement might represent a methodological weakness and could introduce experimental confounds. Thus, aiming at improving our “Peripheral” spatial Stroop, we designed and made available five novel spatial Stroop tasks (Perifoveal, Navon, Figure-Ground, Flanker, and Saliency), wherein the stimuli appeared at the center of the screen. In a within-subjects online study, we compared the six versions to identify which task produced the largest but also the most reliable and robust Stroop effect. Indeed, although internal reliability is frequently overlooked, its estimate is fundamental, also in light of the recently proposed reliability paradox. Data analyses were performed using both the classical general linear model analytical approach and two multilevel modelling approaches (linear mixed models and random coefficient analysis), which specifically served for more accurately estimating the Stroop effect by explaining intra-subject, trial-by-trial variability. We then assessed our results based on their robustness to such analytic flexibility. Overall, our results indicate that the Perifoveal spatial Stroop is the best alternative task for its statistical properties and methodological advantages. Interestingly, our results also indicate that the Peripheral and Perifoveal Stroop effects were not only the largest, but also those with highest and most robust internal reliability.
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