Automaticity of cognitive control: Goal priming in response-inhibition paradigms.

Response inhibition is a hallmark of cognitive control. An executive system inhibits responses by activating a stop goal when a stop signal is presented. The authors asked whether the stop goal could be primed by task-irrelevant information in stop-signal and go/no-go paradigms. In Experiment 1, the task-irrelevant primes GO, ###, or STOP were presented in the go stimulus. Go performance was slower for STOP than for ### or GO. This suggests that the stop goal was primed by task-irrelevant information. In Experiment 2, STOP primed the stop goal only in conditions in which the goal was relevant to the task context. In Experiment 3, GO, ###, or STOP were presented as stop signals. Stop performance was slower for GO than for ### or STOP. These findings suggest that task goals can be primed and that response inhibition and executive control can be influenced by automatic processing. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Balancing cognitive demands: Control adjustments in the stop-signal paradigm.

Cognitive control enables flexible interaction with a dynamic environment. In 2 experiments, the authors investigated control adjustments in the stop-signal paradigm, a procedure that requires balancing speed (going) and caution (stopping) in a dual-task environment. Focusing on the slowing of go reaction times after stop signals, the authors tested 5 competing hypotheses for post-stop-signal adjustments: goal priority, error detection, conflict monitoring, surprise, and memory. Reaction times increased after both successful and failed inhibition, consistent with the goal priority hypothesis and inconsistent with the error detection and conflict hypotheses. Post-stop-signal slowing was greater if the go task stimulus repeated on consecutive trials, suggesting a contribution of memory. We also found evidence for slowing based on more than the immediately preceding stop signal. Post-stop-signal slowing was greater when stop signals occurred more frequently (Experiment 1), inconsistent with the surprise hypothesis, and when inhibition failed more frequently (Experiment 2). This suggests that more global manipulations encompassing many trials affect post-stop-signal adjustments. (PsycINFO Database Record (c) 2011 APA, all rights reserved)     

Development of inhibitory control across the life span.

The stop-signal procedure was used to examine the development of inhibitory control. A group of 275 participants, 6 to 81 years of age, performed a visual choice reaction time (go) task and attempted to inhibit their responses to the go task when they heard a stop signal. Reaction times to the stop and go signals were used to assess performance in inhibition and response execution, respectively. Results indicated the speed of stopping becomes faster with increasing age throughout childhood, with limited evidence of slowing across adulthood. By contrast, strong evidence was obtained for age-related speeding of go-signal reaction time throughout childhood, followed by marked slowing throughout adulthood. Hierarchical regression confirmed that the age-related change in inhibitory control could not be explained by general speeding or slowing of responses. Findings are discussed in regard to the contrast between the development of inhibition and response execution and the utility of the stop-signal procedure. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Dissociating interference-control processes between memory and response.

The ability to mitigate interference is of central importance to cognition. Previous research has provided conflicting accounts about whether operations that resolve interference are singular in character or form a family of functions. Here, the authors examined the relationship between interference-resolution processes acting on working memory representations versus responses. The authors combined multiple forms of interference into a single paradigm by merging a directed-forgetting task, which induces proactive interference, with a stop-signal task, which taps response inhibition processes. The results demonstrated that proactive interference and response inhibition produced distinct behavioral signatures that did not interact. By contrast, combining two different measures of response inhibition by merging a go/no-go task variant and a stop signal produced overadditive behavioral interference, demonstrating that different forms of response inhibition tap the same processes. However, not all forms of response conflict interacted, suggesting that inhibition-related functions acting on response selection are dissociable from those acting on response inhibition. These results suggest that inhibition-related functions for memory and responses are dissociable. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Generalized signaling for control: Evidence from postconflict and posterror performance adjustments.

Goal-directed behavior requires cognitive control to effect online adjustments in response to ongoing processing demands. How signaling for these adjustments occurs has been a question of much interest. A basic question regarding the architecture of the cognitive control system is whether such signaling for control is specific to task context or generalizes across contexts. In this study, the authors explored this issue using a stimulus–response compatibility paradigm. They examined trial-to-trial adjustments, specifically, the findings that incompatible trials elicit improved performance on subsequent incompatible trials and that responses are slower after errors. The critical question was, Do such control effects—typically observed within a single task context—occur across task contexts? The paradigm involved 2 orthogonal, stimulus–response sets: Stimuli in the horizontal direction mapped only to responses in the horizontal direction, and likewise for the vertical direction. Cues indicated that either compatible (same direction as stimulus) or incompatible (opposite to stimulus) responses were required. The results showed that trial-to-trial adjustments exist for both direction-repeat and direction-switch trials, demonstrating that signaling for control adjustments can extend beyond the task context within which they arise. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Semantic matching, response mode, and response mapping as contributors to retroactive and proactive priming.

Two experiments examined proactive and retroactive semantic priming with reported 50-msec primes in 6 target tasks: standard and go/no-go versions of manual lexical decision, vocal lexical decision, and pronunciation. In go/no-go tasks, responses were made only to words. No task differences were found in retroactive priming, which might be a form of proactive priming. Standard manual lexical decision showed more proactive priming, perhaps reflecting response mapping. Go/no-go versions of pronunciation and manual lexical decision showed similar priming, suggesting that semantic matching biases the lexical decision rather than the overt response. Latencies suggested response interference in vocal lexical decision. Exp 3, which included 200-msec primes, did not require prime report. Responses were generally faster, but priming was lower and showed a complex pattern. The tasks tap different underlying processes. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Dissociating consciousness from inhibitory control: Evidence for unconsciously triggered response inhibition in the stop-signal task.

Theories about the functional relevance of consciousness commonly posit that higher order cognitive control functions, such as response inhibition, require consciousness. To test this assertion, the authors designed a masked stop-signal paradigm to examine whether response inhibition could be triggered and initiated by masked stop signals, which inform participants to stop an action they have begun. In 2 experiments, masked stop signals were observed to occasionally result in full response inhibition as well as to yield a slow down in the speed of responses that were not inhibited. The magnitude of this subliminally triggered response time slowing effect correlated with the efficiency measure (stop signal reaction time) of response inhibition across participants. Thus, response inhibition can be triggered unconsciously—more so in individuals who are good inhibitors and under conditions that are associated with efficient response inhibition. These results indicate that in contradiction to common theorizing, inhibitory control processes can operate outside awareness. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

A Response-Discrimination Account of the Simon Effect.

Simon effects might partly reflect stimulus-triggered response activation. According to the response-discrimination hypothesis, however, stimulus-triggered response activation shows up in Simon effects only when stimulus locations match the top-down selected spatial codes used to discriminate between alternative responses. Five experiments support this hypothesis. In Experiment 1, spatial codes of each response differed by horizontal and vertical axis position, yet one axis discriminated between alternative responses, whereas the other did not. Simon effects resulted for targets on discriminating axes only. In Experiment 2, both spatial axes discriminated between responses, and targets on both axes produced Simon effects. In Experiment 3, Simon effects resulted for a spatial choice-reaction task but not for a go/no-go task. Even in the go/no-go task, a Simon effect was restored when a two-choice reaction task preceded the go/no-go task (Experiment 4) or when participants initiated trials with responses spatially discriminated from the go response (Experiment 5). (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

The psychological refractory period of stopping.

The author examined whether the act of control of stopping is subject to the psychological refractory period (PRP) and whether stopping causes a PRP for the processing of subsequent stimuli. The task was to execute or to stop a rapid finger tapping. PRP interference was predicted for double-stimulation trials, in which 2 signals to tap or stop were presented in rapid succession. The experiments showed that stopping ongoing action is subject to and produces PRP interference similar to starting. Responses to signals to continue an ongoing action do not produce PRP interference. The results suggest that selection or initiation of new responses, but not mere response choice, constituted the processing bottleneck that caused the PRP in the present task. Further results indicate that the inhibition of not-yet-executed actions, in contrast to action termination, does not suffer PRP interference and that response inhibitions and terminations should be distinguished. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Externalizing psychopathology and behavioral disinhibition: Working memory mediates signal discriminability and reinforcement moderates response bias in approach–avoidance learning.

Research has suggested that reduced working memory capacity plays a key role in disinhibited patterns of behavior associated with externalizing psychopathology. In this study, participants (N = 365) completed 2 versions of a go/no-go mixed-incentive learning task that differed in the relative frequency of monetary rewards and punishments for correct and incorrect active-approach responses, respectively. Using separate structural equation models for conventional (hit and false alarm rates) and signal detection theory (signal discriminability and response bias) performance indices, distinct roles for working memory capacity and changes in payoff structure were found. Specifically, results showed that (a) working memory capacity mediated the effects of externalizing psychopathology on false alarms and discriminability of go versus no-go signals; (b) these effects were not moderated by the relative frequency of monetary rewards and punishments; (c) the relative frequency of monetary rewards and punishments moderated the effects of externalizing psychopathology on hits and response bias for go versus no-go responses; and (d) these effects were not mediated by working memory capacity. The findings implicate distinct roles for reduced working memory capacity and poorly modulated active approach and passive avoidance in the link between externalizing psychopathology and behavioral disinhibition. (PsycINFO Database Record (c) 2011 APA, all rights reserved)     

Response coding and visuomotor transformation in the Simon task: The role of action goals.

Manual responses can be defined by differing response parameters. Any of them may generate a Simon effect. For all those response parameters, the same implementation of the Simon effect (in terms of subserving mechanism) is assumed. In 3 experiments, subjects had to respond with either fingers or sticks. Temporal properties of the Simon effect changed with response parameters relevant in a task. The Simon effect for manual responses decayed. For stick responses, in which the action goal differed from the anatomical mapping of the acting hand, a sustained Simon effect was observed. However, if the action goal for stick responses was not instrumental for selecting the correct response, the Simon effect decayed. The findings are consistent with the notion of different mechanisms involved in generating a Simon effect. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Redundancy gain in the stop-signal paradigm: Implications for the locus of coactivation in simple reaction time.

The authors carried out 2 experiments designed to cast light on the locus of redundancy gain in simple visual reaction time by using a stop-signal paradigm. In Experiment 1, the authors found that single visual stimuli were more easily inhibited than double visual stimuli by an acoustic stop signal. This result is in keeping with the idea that redundancy gain occurs prior to the ballistic stage of the stop-signal task. In Experiment 2, the authors found that the response to an acoustic go signal was more easily inhibited by a double than by a single visual stop signal. This result provides conclusive evidence for a redundancy gain in the stop process—in a process that does not involve a motor response but rather its inhibition. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Inhibitory Control in Rats Performing a Stop-Signal Reaction-Time Task: Effects of Lesions of the Medial Striatum and d-Amphetamine.

The stop-signal task measures the ability to inhibit a response that has already been initiated, that is, the ability to stop. Imaging studies have implicated frontostriatal circuitry in the mediation of this form of response control. The authors report inhibition functions of normal rats and those with medial striatal damage performing the stop-signal task. Excitotoxic lesions of the medial striatum produced significant deficits on task performance, including increased omissions on the go task and flattened inhibition function, possibly as a result of increased reaction-time mean and variability. Medial striatal lesions also significantly slowed stop-signal reaction time. Subsequent treatment with d-amphetamine removed (0.3 mg/kg) or exacerbated (1.0 mg/kg) this deficit. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Long-term aftereffects of response inhibition: Memory retrieval, task goals, and cognitive control.

Cognitive control theories attribute control to executive processes that adjust and control behavior online. Theories of automaticity attribute control to memory retrieval. In the present study, online adjustments and memory retrieval were examined, and their roles in controlling performance in the stop-signal paradigm were elucidated. There was evidence of short-term response time adjustments after unsuccessful stopping. In addition, it was found that memory retrieval can slow responses for 1-20 trials after successful inhibition, which suggests the automatic retrieval of task goals. On the basis of these findings, the authors concluded that cognitive control can rely on both memory retrieval and executive processes. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

How fast are feedforward postural adjustments of the abdominal muscles?

Abdominal muscles can be activated during rapid but complex motor responses known as feedforward postural adjustments. Exactly how the latency of feedforward adjustments compares with other responses of varying levels of voluntary input and motoneurone excitability remains unclear. Surface electrodes were placed bilaterally over abdominal muscles and over right anterior deltoid (AD) and orbicularis oculi (OO) muscles in eight healthy volunteers. Latencies were obtained during feedforward postural adjustment, acoustic startle reflex, and voluntary activation (respiratory and nonrespiratory) to soft and startling acoustic stimuli. Results showed voluntary activation was fastest for respiratory tasks during mid- or end-expiration. Voluntary activation was also faster when triggered by startling stimuli compared with soft stimuli. These responses were slower than feedforward postural adjustments in all subjects. Feedforward adjustments were slower than acoustic startle reflexes but were somewhat flexible as their amplitude depended on amplitude of AD activation and therefore matched parameters of the movement task. The latency for feedforward postural adjustments of abdominal muscles suggests organization at a low level of the nervous system with limited central processing to match postural responses to movement demands. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Chronometric analysis of apparent spotlight failure in endogenous visual orienting.

Ss made speeded responses to peripheral luminance increments or decrements preceded by informative central precues. In 4 experiments with 48 university students, one of these stimuli was much more likely to occur than the other. In a simple detection task, the likely and unlikely stimuli showed equivalent cuing effects. In a discrimination task (bright/dim), the likely stimuli showed cuing but the unlikely one did not (spotlight failure), and there was a tendency to make the likely response when the unlikely stimulus occurred at the cued location. In Exp 5, the 2 stimuli were equally likely, and a choice was required. Large cuing effects were observed for both stimuli with no evidence of a speed–accuracy trade-off. A logogen-activation framework is described within which criterion and sensitivity adjustments are needed to accommodate the full pattern of results. Endogenous orienting appears to enhance processing of all stimuli at attended (relative to unattended) locations, an effect that may be masked by specific stimulus or response expectancies. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

A model of the go/no-go task.

In this article, the first explicit, theory-based comparison of 2-choice and go/no-go variants of 3 experimental tasks is presented. Prior research has questioned whether the underlying core-information processing is different for the 2 variants of a task or whether they differ mostly in response demands. The authors examined 4 different diffusion models for the go/no-go variant of each task along with a standard diffusion model for the 2-choice variant (R. Ratcliff, 1978). The 2-choice and the go/no-go models were fit to data from 4 lexical decision experiments, 1 numerosity discrimination experiment, and 1 recognition memory experiment, each with 2-choice and go/no-go variants. The models that assumed an implicit decision criterion for no-go responses produced better fits than models that did not. The best model was one in which only response criteria and the nondecisional components of processing changed between the 2 variants, supporting the view that the core information on which decisions are based is not different between them. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

How to stop and change a response: The role of goal activation in multitasking.

Multitasking was studied in the stop-change paradigm, in which the response for a primary GO1 task had to be stopped and replaced by a response for a secondary GO2 task on some trials. In 2 experiments, the delay between the stop signal and the change signal was manipulated to determine which task goals (GO1, GO2, or STOP) were involved in performance and to determine whether the goals were activated in series or in parallel. As the delay increased, the probability of responding on stop trials changed very little, but GO2 task reaction times decreased substantially. Such effects are consistent with both a nondeterministic serial model (in which the GO1 goal is replaced by the STOP goal, which is subsequently replaced by the GO2 goal) and a limited-capacity parallel model (in which stopping and GO2 processing occur concurrently) with a capacity-sharing proportion that resembles serial processing. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Context-sensitive adjustments of cognitive control: Conflict-adaptation effects are modulated by processing demands of the ongoing task.

Dynamic adjustments of cognitive control in response to interference from irrelevant stimulus attributes have repeatedly been shown. The purpose of the current research was to investigate how these control adjustments are modulated by the processing demands of a primary task. To this end, the authors combined a primary task (a number comparison task: classifying digits as smaller or larger than 5) with a Simon task. Control adjustments were observed in the form of typical sequential modulations of the Simon effect. In addition, the authors found sequential modulations of the numerical distance effect and an interaction of both effects. Results suggest that not only response conflict due to interference from task-irrelevant features but also processing demands of task-relevant features determine the level of control adjustment in the subsequent trial. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Audiovisual asynchrony detection in human speech.

Combining information from the visual and auditory senses can greatly enhance intelligibility of natural speech. Integration of audiovisual speech signals is robust even when temporal offsets are present between the component signals. In the present study, we characterized the temporal integration window for speech and nonspeech stimuli with similar spectrotemporal structure to investigate to what extent humans have adapted to the specific characteristics of natural audiovisual speech. We manipulated spectrotemporal structure of the auditory signal, stimulus length, and task context. Results indicate that the temporal integration window is narrower and more asymmetric for speech than for nonspeech signals. When perceiving audiovisual speech, subjects tolerate visual leading asynchronies, but are nevertheless very sensitive to auditory leading asynchronies that are less likely to occur in natural speech. Thus, speech perception may be fine-tuned to the natural statistics of audiovisual speech, where facial movements always occur before acoustic speech articulation. (PsycINFO Database Record (c) 2010 APA, all rights reserved)