Preparatory Interval Research Articles

Proactive selective attention across competition contexts

Selective attention is a cognitive function that helps filter out unwanted information. Theories such as the biased competition model (Desimone & Duncan, 1995) explain how attentional templates bias processing towards targets in contexts where multiple stimuli compete for resources. However, it is unclear how the anticipation of different levels of competition influences the nature of attentional templates, in a proactive fashion. In this study, we used electroencephalography (EEG) to investigate how the anticipated demands of attentional selection (either high or low stimuli competition contexts) modulate target-specific preparatory brain activity and its relationship with task performance. To do so, participants performed a sex/gender judgment task in a cue-target paradigm where, depending on the block, target and distractor stimuli appeared simultaneously (high competition) or sequentially (low competition). Multivariate Pattern Analysis (MVPA) showed that, in both competition contexts, there was a preactivation of the target category to select, with a ramping-up profile at the end of the preparatory interval. However, cross-classification showed no generalization across competition conditions, suggesting different preparatory formats. Notably, time-frequency analyses showed differences between anticipated competition demands, with higher theta band power for high than low competition, which mediated the impact of subsequent stimuli competition on behavioral performance. Overall, our results show that, whereas preactivation of the internal templates associated with the category to select are engaged in advance in high and low competition contexts, their underlying neural patterns differ. In addition, these codes could not be associated with theta power, suggesting that they reflect different preparatory processes. The implications of these findings are crucial to increase our understanding of the nature of top-down processes across different contexts.

Pupillary correlates of preparatory control in the Stroop task.

In three experiments, individual differences in preparatory control in the Stroop task were examined. Participants performed variants of the Stroop task while pupillary responses were examined during the preparatory interval. Variation in working memory capacity was also examined. High Stroop performers tended to demonstrate larger preparatory pupillary responses than low Stroop performers. In Experiment 2, when participants were given pre-cues indicating the congruency of the upcoming trial (MATCHING vs. CONFLICTING), high Stroop performers had larger preparatory pupillary responses for incongruent trials compared to congruent trials, whereas low Stroop performers demonstrated similar preparatory pupillary responses on both incongruent and congruent trials. These results suggest that variation in Stroop performance is partially due to individual differences in the ability to ramp up and regulate the intensity of attention allocated to preparatory control processes. Additionally, there was limited evidence that preparatory control processes partially account for the relation between working memory capacity and performance on the Stroop. Overall, these results provide evidence that individual differences in Stroop performance are partialy due to variation in preparatory control.

Little fast, little slow, should I stay or should I go? Adapting cognitive control to local-global temporal prediction across typical development.

Adaptive cognitive control (CC), the ability to adjust goal-directed behavior according to changing environmental demand, can be instantiated bottom-up by implicit knowledge, including temporal predictability of task-relevant events. In S1-S2 tasks, either local (trial-by-trial hazard expectation) or global (block-by-block expectation) temporal information can induce prediction, allowing for proactive action control. Recent developmental evidence showed that adaptive CC based on global temporal prediction emerges earlier than when it is based on the local one only. However, very little is known about how children learn to dynamically adjust behavior on the fly according to changing global predictive information. Addressing this issue is nevertheless crucial to unravel the mechanisms underlying adaptive CC flexibility. Here we used a modified version of the Dynamic Temporal Prediction task to investigate how typically developing younger (6-8 years) and older children (9-11 years), adolescents (12-15 years) and adults (21-31 years) use global prediction to shape adaptive CC over time. Specifically, the short-long percentage of S2 preparatory intervals was manipulated list-wide to create a slow-fast-slow-fast fixed block sequence and test how efficiently the response speed adapted accordingly. Overall, results revealed that in all groups behavioral performance is successfully adjusted as a function of global prediction in the late phase of the task (block 3 to 4). Remarkably, only adolescents and adults exhibit an early adaptation of adaptive CC (block 1 to 2), while children younger than 11 show sluggish ability in inferring implicit changes in global predictive rules. This age-related dissociation suggests that, although being present from an early age, adaptive CC based on global predictive information needs more developmental space to become flexible in an efficient way. In the light of a neuroconstructivist approach, we suggest that bottom-up driven implicit flexibility may represent a key prerequisite for the development of efficient explicit cognitive control.

Effort Mobilization and Lapses of Sustained Attention.

The current study examined whether effort mobilization would enhance sustained attention and reduce lapses of attention. Participants performed a sustained attention task and were randomly assigned to either an effort condition where they were instructed to "Try Hard" on a subset of trials or were assigned to a control condition with no "Try Hard" instructions. Pupillary responses were continuously recorded, and periodically during the task participants were presented with thought probes to determine whether they were on or off task. The results suggested within the effort condition there were no behavioral differences between Try Hard and "Standard" trials. Preparatory pupil responses were increased in Try Hard trials, but there were no differences for phasic pupillary responses to stimulus onset. In contrast, examining differences between the effort and control conditions suggested that participants who received the Try Hard instructions demonstrated faster overall performance, a reduction in very long reaction times, and reported fewer off-task thoughts compared with participants in the control condition. Participants in the effort condition also demonstrated a larger ramp-up in pupillary responses during the preparatory interval and a larger phasic response to stimulus onset compared with participants in the control condition. These results are consistent with attention allocation models suggesting that participants in the effort condition mobilized more attentional effort than participants in the control condition, resulting in enhanced sustained attention and a reduction in lapses of attention. These results also are consistent with recent theories, which suggest that the locus coeruleus norepinephrine system is associated with effort mobilization.

Temporal preparation in adults with autistic spectrum disorder: The variable foreperiod effect.

Research suggested the possibility that temporal cognition may be different in autistic spectrum disorder (ASD). Although there are some empirical studies examining timing ability in these individuals, to our knowledge, no one directly assessed the ability to predict when an event will occur. Here, we report a study on implicit temporal preparation in individuals with ASD as indexed by the variable foreperiod (FP) effect. We compared a group of adult ASD participants to a group of typically-developed (TD) controls, for their respective abilities to utilize implicit temporal information in a simple detection task with three different preparatory intervals (FP, short, middle and long). Participants were given a warning tone to signal an imminent stimulus, and asked to press a key as quickly as they could upon detection of the stimulus. Both groups were able to use implicit temporal information, as revealed by both the variable-FP effect (i.e., faster response for targets appearing after a long FP) and asymmetric sequential effects (i.e., slower response in short-FP trials following a previous long-FP trial). The TD group exhibited a faster response in a long-FP trial that was preceded by short-FP one, whereas the ASD group did not, as reflected in their higher percentage of response omissions for a target that appeared later than in the previous trial. The reduced ability of ASD participants to modulate their responses under these conditions might reflect a difficulty in time-based monitoring of stimulus occurrence. LAY SUMMARY: Time-processing may be different in autistic spectrum disorder (ASD). This study addressed the ability to anticipate a relevant stimulus's onset according to predictable interstimulus intervals comparing adults with ASD and typically developed controls. We found that ASD participants did not benefit from temporal preparation when stimulus appeared later than previously attended. This suggests a reduced ability in detecting implicit temporal regularities between events.

The Effect of Probabilistic Context on Implicit Temporal Expectations in Down Syndrome.

One of the most important sources of predictability that human beings can exploit to create an internal representation of the external environment is the ability to implicitly build up subjective statistics of events’ temporal structure and, consequently, use this knowledge to prepare for future actions. Stimulus expectancy can be subjectively shaped by hierarchically nested sources of prediction, capitalizing on either local or global probabilistic rules. In order to better understand the nature of local-global proactive motor control in Down Syndrome, in the present study a group of participants with Down Syndrome (DS group; n = 28; mean age 29.5 ± 13 years; range 10–54) and a group of typically developing participants matched by either gender or mental age (TD-MA group; n = 28; 5.6 ± 1 years; range 4–8) were administered a novel motor preparation task, defined as the Dynamic Temporal Prediction (DTP) task. In the DTP, the temporal preparation to imperative stimuli is implicitly shaped by the local increase of expectancy. This is manipulated trial-by-trial as a function of the preparatory foreperiod interval (Stimulus-Onset Asynchrony or SOA). In addition, temporal preparation can be also implicitly adjusted as a function of global predictive context, so that a block-wise SOA-distribution bias toward a given preparatory interval might determine a high-order source of expectancy, with functional consequences on proactive motor control adjustment. Results showed that in both groups motor preparation was biased by temporal expectancy when this was locally manipulated within-trials. By contrast, only the TD-MA group was sensitive to global rule changes: only in this cohort was behavioral performance overall impacted by the SOA probabilistic distribution manipulated between-blocks. The evidence of a local-global dissociation in DS suggests that the use of flexible cognitive mechanisms to implicitly extract high-order probabilistic rules in order to build-up an internal model of the temporal properties of events is disrupted in this developmental disorder. Moreover, since the content of the information to be processed in the DTP task was neither verbal nor spatial, we suggest that atypical global processing in Down Syndrome is a domain-general rather than specific aspect characterizing the cognitive profile of this population.

When is the brain ready for mental actions? Readiness potential for mental calculations

While the preparatory neural mechanisms of real and imagined body movements have been extensively studied, the underpinnings of self‑initiated, voluntary mental acts are largely unknown. Therefore, using electroencephalography (EEG), we studied the time course and patterns of changes in brain activity associated with purely mental processes which start on their own, without an external or interoceptive stimulation. We compared EEG recordings for decisions to perform mental operations on numbers, imagined finger movements, and actual finger movements. In all three cases, we found striking similarities in slow negative shifts of brain electrical activity lasting around 1 s and, therefore, characteristic for readiness potential. These results show that the brain not only needs time to be ready for a purely mental task but also that a required preparatory interval involves neural changes analogical to the ones observed before intentional body movements. As such, the readiness potential represents a universal process of unconscious preparatory brain activity preceding any, including purely mental, voluntary action.

Internalising symptoms and verbal working memory in school-age children: A processing efficiency analysis.

The current study investigated differential contributions of internalising symptoms (state anxiety, trait anxiety, depression) to school-age children's verbal short-term (STM) and working memory (WM) span accuracy and efficiency (microanalysis of response times). Children's (N = 125, Mage = 11.44 years) STM/WM was assessed with simple/complex span tasks. Our analyses revealed that: (a) children with high levels of state anxiety displayed reduced simple span accuracy (on Word span) and poorer efficiency on both simple (preparatory intervals, interword pauses) and complex span (preparatory intervals) response time segments; (b) trait anxiety was a negative predictor of children's complex span accuracy, as well as their efficiency on both simple (word durations) and complex span (interword pauses) response time measures; (3) depressive symptoms predicted longer simple span interword pauses. Findings indicate that while all internalising symptoms were predictive of children's poorer memory search efficiency, especially during the "silent", executive intervals (interword pauses), anxiety symptoms were specifically predictive of children's impaired span accuracy and other efficiency indicators (preparatory intervals, word durations). The study highlights the differential contributions of state, trait anxiety, and depressive symptoms to STM/WM in children, emphasising the need to measure both accuracy and efficiency to assess the role that such symptoms play in children's performance.

When specific action biases meet nonspecific preparation: Event repetition modulates the variable-foreperiod effect.

Preparing for the moment of action speeds up reaction time (RT) performance even if the particular response is unknown beforehand. When the preparatory interval, or foreperiod (FP), varies unpredictably between trials, responses usually become faster with increasing FP length. This variable-FP effect has been demonstrated to partly originate from trial-to-trial sequential effects of FP length, which are asymmetric as they occur mainly in short-FP but not in long-FP trials. In two experiments, we examined whether and how event-specific biases arising from previous target processing and responding affect both variable-FP and sequential FP effects. We found that trial-to-trial repetitions (vs. alternations) of imperative events produced response time benefits in short-FP but not in long-FP trials, almost eliminating the variable-FP effect, while the sequential FP effect remained intact. This asymmetric contribution to speeded performance in variable-FP settings suggests that sequential event-specific biases may be highly transient and not necessarily an integral part of the mental representations that guide time-based expectancy, or may be overridden by high levels of nonspecific preparation in long-FP trials. In conclusion, temporal preparation appears to be a nonspecific mechanism (i.e., generally not bound to particular event features) for prioritizing certain positions on the mental time line, on which event-specific short-term biases are superimposed if time-based preparation is weak. (PsycINFO Database Record

Foggy windows: Pupillary responses during task preparation.

We investigated pupil dilation in 96 subjects during task preparation and during a post-trial interval in a visual search task and an auditory working memory task. Completely informative difficulty cues (easy, medium, or hard) were presented right before task preparation to examine whether pupil dilation indicated advance mobilisation of attentional resources; functional magnetic resonance imaging (fMRI) studies have argued for the existence of such task preparation, and the literature shows that pupil dilation tracks attentional effort during task performance. We found, however, little evidence for such task preparation. In the working memory task, pupil size was identical across cues, and although pupil dilation in the visual search task tracked the cue, pupil dilation predicted subsequent performance in neither task. Pupil dilation patterns in the post-trial interval were more consistent with an effect of emotional reactivity. Our findings suggest that the mobilisation of attentional resources in the service of the task does not occur during the preparatory interval, but is delayed until the task itself is initiated.

Both facilitatory and inhibitory impairments underlie age-related differences of proactive cognitive control across the adult lifespan

We investigated two components of proactive cognitive control, response facilitation and response inhibition, in an adult lifespan sample (N=544, age range=18–91years) by administering two response-preparation tasks: a procue task, primarily involving facilitation, and an anticue task, involving both facilitation and inhibition. Cues in both tasks corresponded with the index and middle fingers of either the left or right hand. After a random preparation interval (PI) of 100–850ms following the onset of the cue signal, a single-target stimulus indicated the required response. Where procues were spatially aligned with the two fingers of the responding hand, anticues consistently indicated the two fingers of the opposite hand, requiring a remapping of cue location and response hand. This remapping requires inhibition to suppress the automatic activation of the ipsilateral responses. Previous research revealed typical reaction time (RT) profiles for procues and anticues as a function of PI. Whereas procues generate RT benefits (relative to a neutral-cue condition) already at short PIs, which increase with longer PIs, anticues generate RT costs at short PIs and RT benefits at longer PIs. Our results showed that, in the anticue task, older participants needed more preparation time to turn RT costs into RT benefits than younger participants, revealing an age-related deficit of response inhibition. Moreover, in both tasks, older participants were less able to increase RT benefits with longer PIs, revealing a deficit of response facilitation. We conclude that both facilitatory and inhibitory impairments contribute to age-related deficiencies in proactive cognitive control.

Nonspecific Inhibition of the Motor System during Response Preparation.

Motor preparation entails the recruitment of excitatory and inhibitory neural mechanisms. The current experiments address the specificity of inhibitory mechanisms, asking whether preparatory inhibition affects task-irrelevant muscles. Participants prepared a finger movement to be executed at the end of a short delay period. Transcranial magnetic stimulation over primary motor cortex provided an assay of corticospinal excitability. Consistent with earlier work, the agonist muscle for the forthcoming response was inhibited during the preparatory period. Moreover, this inhibition was evident in task-irrelevant muscles, although the magnitude of inhibition depended on whether the response was fixed or involved a choice. These results implicate a broadly tuned inhibitory mechanism that facilitates response preparation, perhaps by lowering background activity before response initiation.

Spectro-temporal Unfolding of Temporal Orienting of Attention

All behaviors unfold over time, therefore, our ability to perceive and adapt our behavior according to the temporal constraints of our environment is likely a fundamental requirement for successful behavior (Nobre et al., 2007). Temporal preparation has been defined as our ability to anticipate and prepare an optimal response to forthcoming events in our environment (Nobre et al., 2007). Temporal preparation requires integration of different types of temporal information. On the one hand, information can be provided by temporal predictions, i.e. temporal orienting of attention. On the other hand, information can be afforded by the duration of the previous temporal events, namely the sequential effects (e.g., Capizzi et al., 2012). In this project we are focusing in the time-frequency analysis during the delay period (i.e., foreperiod) from the cue onset until the target onset at the short interval. We followed the results of Capizzi et al.’s (2013) study which showed that the CNV component was increased in the delay period when the previous foreperiod was short as compared to long (Cappizi et al., 2013).Recent studies are concerned with the question of how oscillatory brain activity can provide a mechanism for regulating our temporal behavior (Cravo et al., 2011; Praamstra & Pope, 2007; Rohenkohl & Nobre, 2011). Oscillatory brain activity may be one of the mechanisms underlying the operation of different brain areas during cognitive functions (Buzsaki, 2006). When brain activity is recorded at the level of neural populations, the activity assumes a rhythmic temporal structure. Spectral analysis or time-frequency analysis is the study of brain rhythms. Using time-frequency analysis one can characterize the modulation of certain brain rhythms as those unfold in time. Additionally, different brain regions can engage in synchronized brain activity in certain frequency bands. Such synchronization may support inter-areal communication, which is likely fundamental to many of the cognitive functions producing behavior. Studying brain rhythms therefore has the potential of revealing mechanisms underlying cognitive function and behavior (Fries, 2009).Previous studies in the field of temporal preparation (Cravo et al., 2011; Rohenkohl & Nobre, 2011) have investigated oscillatory brain activity and how it is modulated over the time intervals in which target events are expected. Specifically, desynchronization of low frequency power (<30Hz) has been documented following the time course of predictable time intervals. In this project, we were interested in investigating the spectro-temporal profile of both temporal orienting and the sequential effects during the preparatory interval (foreperiod). Time/frequency analyses was focused on epochs locked to the cue onset and compared EEG activity related to early vs. late temporal expectations (temporal orienting) and EEG activity related to previous short vs. previous long foreperiods (sequential effects).With the aforementioned approach we aim to clarify whether or not sequential effects and temporal orienting effects are mediated by the same brain activity. The behavioral data from the previous study of Capizzi et al. (2012) indicated that temporal orienting and sequential effects are different aspects of temporal preparation and that sequential effects are related to automatic rather than to controlled processing unlike the temporal orienting effect. Time frequency analysis was performed in a total of fourteen subjects; cue locked analysis showed that when an early cue is followed by a short interval there is higher power in lower frequencies as compared to the power when a late cue is followed by a short interval. These results signify a difference in the power representation of the temporal preparation for explicit cuing compared when temporal preparation is guided by the presentation of a regular rhythm suggesting the involvement of dissociable mechanisms

Contribution of reactive and proactive control to children's working memory performance: Insight from item recall durations in response sequence planning.

The present study addressed whether developmental improvement in working memory span task performance relies upon a growing ability to proactively plan response sequences during childhood. Two hundred thirteen children completed a working memory span task in which they used a touchscreen to reproduce orally presented sequences of animal names. Children were assessed longitudinally at 7 time points between 3 and 10 years of age. Twenty-one young adults also completed the same task. Proactive response sequence planning was assessed by comparing recall durations for the 1st item (preparatory interval) and subsequent items. At preschool age, the preparatory interval was generally shorter than subsequent item recall durations, whereas it was systematically longer during elementary school and in adults. Although children mostly approached the task reactively at preschool, they proactively planned response sequences with increasing efficiency from age 7 on, like adults. These findings clarify the nature of the changes in executive control that support working memory performance with age.

N − 2 repetition costs depend on preparation in trials n − 1 and n − 2.

In task switching, a common result supporting the notion of inhibitory processes as a determinant of switch costs is the occurrence of n - 2 repetition costs. Evidence suggests that this effect is not affected by preparation. However, the role of preparation on preceding trials has been neglected so far. In this study, evidence for an influence of preparatory processes on n - 2 repetition costs is provided by focusing on the cue-target interval on trials n - 1 and n - 2. N - 2 repetition costs were affected by an interaction of both n - 1 and n - 2 preparation time, being more pronounced when both preparatory intervals were long. The results provide support for the notion of active preparation processes involved in backward inhibition.

Tracing the bilingual advantage in cognitive control: The role of flexibility in temporal preparation and category switching

The present study addressed the question whether bilinguals are characterised by increased cognitive flexibility. Mechanisms of cognitive flexibility were compared between a group of Hungarian-Polish bilinguals and a group of Hungarian monolinguals. The first task explored the effects of temporal orienting (ability to voluntarily orient attention to a certain point in time when a relevant event is expected) and the efficiency of switching between preparatory time intervals of different duration (sequential effects). The second task – the social category switching task – tapped into the mechanisms of switching between 2 types of categories (age and gender) and employed socially relevant stimuli (faces). The results of the first task revealed similar temporal orienting effects for both groups; however, the pattern of sequential effects differed between the groups, showing that bilinguals were less affected by the duration of the preceding preparatory interval. In the social category switching task, bilinguals showed reduced switch costs in the RT measure when categorising gender, and greater accuracy in the specific switch and no-switch conditions. We suggest that bilinguals are characterised by an enhanced mechanism of cognitive flexibility, which is applied to a temporal domain (efficient switching between preparatory intervals of different duration), and extends to the cognitive control processes in social categorisation tasks.

Cortical sources of ERP in prosaccade and antisaccade eye movements using realistic source models.

The cortical sources of event-related-potentials (ERP) using realistic source models were examined in a prosaccade and antisaccade procedure. College-age participants were presented with a preparatory interval and a target that indicated the direction of the eye movement that was to be made. In some blocks a cue was given in the peripheral location where the target was to be presented and in other blocks no cue was given. In Experiment 1 the prosaccade and antisaccade trials were presented randomly within a block; in Experiment 2 procedures were compared in which either prosaccade and antisaccade trials were mixed in the same block, or trials were presented in separate blocks with only one type of eye movement. There was a central negative slow wave occurring prior to the target, a slow positive wave over the parietal scalp prior to the saccade, and a parietal spike potential immediately prior to saccade onset. Cortical source analysis of these ERP components showed a common set of sources in the ventral anterior cingulate and orbital frontal gyrus for the presaccadic positive slow wave and the spike potential. In Experiment 2 the same cued- and non-cued blocks were used, but prosaccade and antisaccade trials were presented in separate blocks. This resulted in a smaller difference in reaction time between prosaccade and antisaccade trials. Unlike the first experiment, the central negative slow wave was larger on antisaccade than on prosaccade trials, and this effect on the ERP component had its cortical source primarily in the parietal and mid-central cortical areas contralateral to the direction of the eye movement. These results suggest that blocked prosaccade and antisaccade trials results in preparatory or set effects that decreases reaction time, eliminates some cueing effects, and is based on contralateral parietal-central brain areas.

Differential Go/NoGo activity in both contingent negative variation and spectral power.

We investigated whether both the contingent negative variation (CNV), an event-related potential index of preparatory brain activity, and event-related oscillatory EEG activity differentiated Go and NoGo trials in a delayed response task. CNV and spectral power (4–100 Hz) were calculated from EEG activity in the preparatory interval in 16 healthy adult participants. As previously reported, CNV amplitudes were higher in Go compared to NoGo trials. In addition, event-related spectral power of the Go condition was reduced in the theta to low gamma range compared to the NoGo condition, confirming that preparing to respond is associated with modulation of event-related spectral activity as well as the CNV. Altogether, the impact of the experimental manipulation on both slow event-related potentials and oscillatory EEG activity may reflect coordinated dynamic changes in the excitability of distributed neural networks involved in preparation.

Anxiety, a benefit and detriment to cognition: Behavioral and magnetoencephalographic evidence from a mixed-saccade task

Anxiety is typically considered an impediment to cognition. We propose anxiety-related impairments in cognitive-behavioral performance are the consequences of enhanced stimulus-driven attention. Accordingly, reflexive, habitual behaviors that rely on stimulus-driven mechanisms should be facilitated in an anxious state, while novel, flexible behaviors that compete with the former should be impaired. To test these predictions, healthy adults (N=17) performed a mixed-saccade task, which pits habitual actions (pro-saccades) against atypical ones (anti-saccades), under anxiety-inducing threat of shock and safe conditions. Whole-head magnetoencephalography (MEG) captured oscillatory responses in the preparatory interval preceding target onset and saccade execution. Results showed threat-induced anxiety differentially impacted response times based on the type of saccade initiated, slowing anti-saccades but facilitating erroneous pro-saccades on anti-saccade trials. MEG source analyses revealed that successful suppression of reflexive pro-saccades and correct initiation of anti-saccades during threat was marked by increased theta power in right ventrolateral prefrontal cortical and midbrain regions (superior colliculi) implicated in stimulus-driven attention. Theta activity may delay stimulus-driven processes to enable generation of an anti-saccade. Moreover, compared to safety, threat reduced beta desynchronization in inferior parietal cortices during anti-saccade preparation but increased it during pro-saccade preparation. Differential effects in inferior parietal cortices indicate a greater readiness to execute anti-saccades during safety and to execute pro-saccades during threat. These findings suggest that, in an anxiety state, reduced cognitive-behavioral flexibility may stem from enhanced stimulus-driven attention, which may serve the adaptive function of optimizing threat detection.

Electrophysiological correlates of preparation and implementation for different types of task shifts

The ability to flexibly shift between tasks is central to cognitive control, but whether the same brain mechanisms mediate shifting across different tasks is unknown. In this study, we investigated whether variations in stimulus-dimensions or response-mapping might influence task switching in terms of its preparatory processes, as reflected in cue-locked event-related potentials (ERPs), and its implementation processes, as reflected in stimulus-locked ERPs. Participants judged pairs of digits as same or different in one of two conditions. In one condition, the task-relevant stimulus-dimension was either repeated or switched across trials while the response-mapping rule was kept constant. In the other condition, the task-relevant stimulus-dimension was kept constant while the response-mapping rule was repeated or switched across trials. The length of the preparatory interval was manipulated. Data revealed switch-related preparatory ERP components (including N2 and a late slow positivity) that were associated with both types of task shifting and an N400-like negativity that distinguished between the two types. Several switch-related implementation ERP components associated with both types of task shifting were found at posterior sites. Distinct frontal modulations of the N1, P2, and N2 were found to associate with the implementation of the response-mapping shift, whereas a slow positivity was associated with the implementation of the stimulus-dimension shift. Therefore, this study demonstrates that there are shared and distinct processes across different types of task shifting. Finally, because the same transition-cue was used for different task shifts, the distinct processes cannot be explained simply by differences in cue processing.