The duration of response inhibition in the stop-signal paradigm varies with response force

In a previous study, we have found that the speed of stopping a response is delayed when response readiness is reduced by cuing the probability of no-go trials [Acta Psychol. 111 (2002) 155]. Other investigators observed that responses are more forceful when the probability to respond is low than when it is high (e.g. [Quart. J. Exp. Psychol. A 50 (1997) 405]). In this study, the hypothesis was tested that low probability responses are more forceful than high probability responses and that these responses are more difficult to stop. Subjects performed on a choice reaction task and on three tasks with respectively 100%, 80%, and 50% response probabilities. Stop signals were presented on 30% of the trials, instructing subjects to withhold their response. Response force on non-signal (go) trials and the duration of response inhibition on signal (stop) trials increased as response probability decreased. This pattern of findings was interpreted to support the hypothesis predicting that stopping is more difficult when response readiness is low than when it is high.     

The interplay of stop signal inhibition and inhibition of return

Inhibition of return (IOR) refers to slower responding to a stimulus that appears in the same rather than a different location as that of a preceding stimulus. The goal of the present study was to examine the relationship between IOR and stop signal inhibition. Participants were presented with two stimuli (S1 and S2) on each trial. On half of the trials (go trials), participants were required to make a speeded button-press response to report the location of S1; on the other half of trials (stop trials), they were required to cancel the response to S1, as indicated by the appearance of a stop signal at a variable delay (stop signal delay, SSD) after the appearance of S1. Success in cancelling an S1 response varied directly as a function of the SSD: The longer the delay, the more difficult it was for participants to cancel the prepared response. We examined the magnitude of IOR in the S2 reaction times as a function of whether participants made a correct go response to S1, made an erroneous non-cancelled response to S1, or successfully cancelled a response to S1. Our results indicated that the presentation of a stop signal increased the magnitude of IOR, even when the S1 response was not successfully cancelled. However, this was true only when the to-be-cancelled response involved the same effectors as the response used to reveal IOR. These results suggest that there may be a motor component to IOR that is sensitive to the same inhibitory processes that are used to cancel responses in a stop signal paradigm.     

IMPULSIVITY AND INHIBITORY CONTROL

Abstract— We report an experiment testing the hypothesis that impulsive behavior reflects a deficit in the ability to inhibit prepotent responses Specifically, we examined whether impulsive people respond more slowly to signals to inhibit (stop signals) than non-impulsive people In this experiment, 136 undergraduate students completed an impulsivity questionnaire and then participated in a stop-signal experiment, in which they performed a choice reaction time (go) task and were asked to inhibit their responses to the go task when they heard a stop signal The delay between the go signal and the stop signal was determined by a tracking procedure designed to allow subjects to inhibit on 50% of the stop-signal trials. Reaction time to the go signal did not vary with impulsivity, but estimated stop-signal reaction time was longer in more impulsive subjects, consistent with the hypothesis and consistent with results from populations with pathological problems with impulse control.     

Restraint and Cancellation: Multiple Inhibition Deficits in Attention Deficit Hyperactivity Disorder

We used variations of the stop signal task to study two components of motor response inhibition—the ability to withhold a strong response tendency (restraint) and the ability to cancel an ongoing action (cancellation)—in children with a diagnosis of attention deficit hyperactivity disorder (ADHD) and in non-ADHD controls of similar age (ages 7–14 years). The goal was to determine if restraint and cancellation were related and if both were deficient in ADHD. The stop signal task involved a choice reaction time task (go task) which required a rapid response. The demand for inhibitory control was invoked through the presentation of a stop signal on a subset of go trials which required that the ongoing response be suspended. The stop signal was presented either concurrently with the go signal (restraint version) or after a variable delay (cancellation version). In Study 1, we compared ADHD and control children on the cancellation version of the stop task; in Study 2, we compared ADHD and controls on the restraint version. In Study 3, a subset of ADHD and control participants completed both tasks so that we could examine convergence of these dimensions of inhibition. Compared to control participants, ADHD participants showed a deficit both in the ability to cancel and to restrain a speeded motor response. Performance on the restraint version was significantly correlated with performance on the cancellation version in controls, but not in ADHD participants. We conclude that ADHD is associated with deficits in both restraint and cancellation subcomponents of inhibition.     

Developmental trends in simple and selective inhibition of compatible and incompatible responses

This study examined age-related change in the ability to inhibit responses using two varieties of the stop signal paradigm. Three age groups (29 7-year-olds, 24 10-year-olds, and 28 young adults) performed first on a visual choice reaction task in which the spatial mapping between the go signal and response was varied between blocks. The choice task was then complicated by randomly inserting a visual stop signal on 30% of the trials. In the simple stop signal paradigm, the stop signal required the inhibition of the planned response. In the selective stop signal paradigm, the stop signal required response inhibition only when the stop signal was presented at the same side as the instructed response to the go signal. The results showed that simple stopping was faster than selective stopping and that selective, but not simple, stopping of incompatible responses was slower than stopping of compatible responses. Brinley plot analysis yielded linear functions relating children's latencies to adults' latencies. Analysis of shared variance indicated that developmental change in the speed of selective stopping continued to be significant even when the effect associated with simple stopping was removed. This pattern of findings is discussed vis-à-vis notions of global versus specific developmental trends in the speed of information processing.     

Response preparation and code overlap in dual tasks

In a dual-task paradigm, a visual-encoding task with a deferred verbal report of a moving target was combined with a speeded task, in which participants prepared a precued leftward or rightward key-press response that was withheld until an auditory go signal. We manipulated the interval between the response cue and the target for the visual-encoding task, the interval between this target and the go signal, and spatial cross-task compatibility between the direction of the target movement in the visual task and the speeded manual response. The results of two experiments suggest that visual encoding interferes with response preparation and with the initiation of the prepared manual response at a short target-go interval. Also, responses were faster in compatible than in incompatible trials, indicating a cross-task compatibility effect. Experiment 2 reversed this compatibility effect by instruction, suggesting that the compatibility effect is based on response-response overlap. In both experiments, response preparation impaired accuracy in the visual task. Taken together, these results suggest that response processes and visual encoding share common codes and processes.     

Trial-to-trial sequential dependencies in a social and non-social Simon task

Recent research has shown that joint-action effects in a social Simon task provide a good index of action co-representation. The present study aimed to specify the mechanisms underlying joint action by considering trial-to-trial transitions. Using non-social stimuli, we assigned a Simon task to two participants. Each was responsible for only one of two possible responses. This task was performed alone (Individual go/nogo task) and in cooperation with another person who was sitting alongside (Joint go/nogo task). As a further control task, we added a Standard Simon task. Replicating previous findings (Sebanz et al. in Cognition 88:B11-B21, 2003), we found no spatial compatibility effect in the Individual go/nogo task but we did find one in the Joint go/nogo task. A more detailed analysis showed that a sequential modulation of the Simon effect was present in both the Joint and the Individual go/nogo tasks. We found reliable Simon effects in trials following Simon compatible trials not only in the Joint go/nogo task but also to a somewhat smaller extent in the Individual go/nogo task. For both these go/nogo tasks, sequential modulation effects were stronger for nogo/go transitions than for go/go transitions. This suggests that low-level feature binding and repetition mechanisms contribute to the social Simon effect related to the specific requirement not to respond on nogo trials.     

Effects of stop-signal probability in the stop-signal paradigm: the N2/P3 complex further validated

The aim of this study was to examine the effects of frequency of occurrence of stop signals in the stop-signal paradigm. Presenting stop signals less frequently resulted in faster reaction times to the go stimulus and a lower probability of inhibition. Also, go stimuli elicited larger and somewhat earlier P3 responses when stop signals occurred less frequently. Since the amplitude effect was more pronounced on trials when go signals were followed by fast than slow reactions, it probably reflected a stronger set to produce fast responses. N2 and P3 components to stop signals were observed to be larger and of longer latency when stop signals occurred less frequently. The amplitude enhancement of these N2 and P3 components were more pronounced for unsuccessful than for successful stop-signal trials. Moreover, the successfully inhibited stop trials elicited a frontocentral P3 whereas unsuccessfully inhibited stop trials elicited a more posterior P3 that resembled the classical P3b. P3 amplitude in the unsuccessfully inhibited condition also differed between waveforms synchronized with the stop signal and waveforms synchronized with response onset whereas N2 amplitude did not. Taken together these findings suggest that N2 reflected a greater significance of failed inhibitions after low probability stop signals while P3 reflected continued processing of the erroneous response after response execution.     

Countermanding saccades: evidence against independent processing of go and stop signals

In a stop signal paradigm, subjects were instructed to make a saccade to a visual target appearing left or right of the fixation point. In 25% of the trials, an auditory stop signal was presented after a variable delay that required the subject to inhibit the saccade. Observed saccadic response times in stop failure trials were longer than predicted by Logan and Cowan's (1984) race model. Saccadic response time and amplitude decreased with the time between stop signal presentation and saccade execution, suggesting an inhibitory effect between the stop signal and the go signal processes that is not compatible with an independent race assumption. Moreover, countermanding a saccade was more difficult when stop and go signals appeared at the same location.     

On the ability to inhibit simple and choice reaction time responses: a model and a method

This article reports four experiments on the ability to inhibit responses in simple and choice reaction time (RT) tasks. Subjects responding to visually presented letters were occasionally presented with a stop signal (a tone) that told them not to respond on that trial. The major dependent variables were (a) the probability of inhibiting a response when the signal occurred, (b) mean and standard deviation (SD) of RT on no-signal trials, (c) mean RT on trials on which the signal occurred but subjects failed to inhibit, and (d) estimated RT to the stop signal. A model was proposed to estimated RT to the stop signal and to account for the relations among the variables. Its main assumption is that the RT process and the stopping process race, and response inhibition depends on which process finishes first. The model allows us to account for differences in response inhibition between tasks in terms of transformations of stop-signal delay that represent the relative finishing times of the RT process and the stopping process. The transformations specified by the model were successful in group data and in data from individual subjects, regardless of how delays were selected. The experiments also compared different methods of selecting stop-signal delays to equate the probability of inhibition in the two tasks.     

Task switching and shifting between stopping and going: Developmental change in between-trial control adjustments

This study set out to investigate developmental differences in the ability to switch between choice tasks and to shift between Go/NoGo and choice tasks. Three age groups (7-year-olds, 11-year-olds, and young adults) were asked to consider the shape or color of a bivalued target stimulus. The participants performed a switch task in which a cue signaled the task to be performed (i.e., respond to shape vs. respond to color) and a shift task in which a cue instructed them to make a choice reaction to the shape of the stimulus or to respond (Go) versus inhibit (NoGo) to the color of the stimulus. The ability to switch was examined by considering choice-choice switches versus choice-choice repeats. The ability to shift was examined by considering NoGo-to-choice shifts versus choice-choice repeats and NoGo-to-Go shifts versus Go-Go repeats. The results showed that responding on Go trials was delayed following response inhibition on a NoGo trial. This delay did not discriminate between age groups. Responding on choice trials was considerably slowed when following response inhibition on NoGo trials. This slowing decreased with advancing age. Finally, responses on switch trials were slower compared with repeat trials, and this slowing was disproportionately large in young children compared with the other two age groups. This pattern of findings was interpreted in terms of a generic mechanism involving between-trial control adjustments in the setting of response thresholds that are likely to be mediated by a complex neural network implicating the dorsolateral prefrontal cortex and the presupplementary motor cortex.     

An electrophysiological study of the insertion of overt response choice

Using electrophysiological measures, the authors studied changes in prestimulus state, stimulus identification, and response-related processing when, in a go/no-go task, forced choice between 2 overt go responses was inserted. The authors observed decreased prestimulus motor preparation (electromyogram), no change in stimulus identification time (selection negativity), a minor increase in response selection time (lateralized readiness potential), a large increase in response preparation time (lateralized readiness potential), a minor effect on response execution time (electromyogram), and a decrease in the activation of a response-inhibition process on no-go trials (frontal event-related potential). The existence of the response-inhibition process was verified by the presence of inverted lateralized readiness potentials on no-go trials. Pure insertion of response choice in a task seems impossible because the choice between activation and inhibition (go/no-go) always seems already present.     

Response inhibition during perceptual decision making in humans and macaques

Response inhibition in stop signal tasks has been explained as the outcome of a race between GO and STOP processes (e.g., Logan, 1981). Response choice in two-alternative perceptual categorization tasks has been explained as the outcome of an accumulation of evidence for the alternative responses. To begin unifying these two powerful investigation frameworks, we obtained data from humans and macaque monkeys performing a stop signal task with responses guided by perceptual categorization and variable degrees of difficulty, ranging from low to high accuracy. Comparable results across species reinforced the validity of this animal model. Response times and errors increased with categorization difficulty. The probability of failing to inhibit responses on stop signal trials increased with stop signal delay, and the response times for failed stop signal trials were shorter than those for trials with no stop signal. Thus, the Logan race model could be applied to estimate the duration of the stopping process. We found that the duration of the STOP process did not vary across a wide range of discrimination accuracies. This is consistent with the functional, and possibly mechanistic, independence of choice and inhibition mechanisms.     

Changes in spinal reflex excitability in a countermanded timed response task

Subjects (N = 8) performed a timed response task in which they attempted to synchronize an impulsive foot-press response with the last in a series of four regularly spaced tones. In Experiment 1, the response was countermanded on one third of the trials (stop trials) by a stop signal that appeared at a predetermined delay after the third tone. No stop signal appeared on the remaining trials (go trials). All subjects showed a systematic transition from withholding the response on stop trials in which the stop signal appeared shortly after the third tone to executing the response on trials in which a single stop signal delay had been chosen so that a response would be made on about 50% of the stop trials. We elicited Hoffmann (H) reflexes from the soleus muscle on all trials to determine whether the reflexes were augmented on occasions on which a response was prepared but withheld. Mean H-reflex amplitudes on go trials and on stop trials on which the response was executed were similar and showed a marked augmentation beginning about 250 ms before response onset; mean H-reflex amplitudes on stop trials on which the response was withheld showed less pronounced augmentation. Inspection of individual H-reflex amplitudes revealed that on stop trials on which the response was withheld the reflexes could be augmented to the same extent as on trials on which the response was executed. This dissociation of H-reflex augmentation and response execution shows that H-reflex augmentation reflects a controlled response process. Ballistic response processes therefore must be limited to a brief duration.     

Facilitating and inhibiting effects of priming and selection criteria in a sequence of dichotic listening trials

Competing models of attention make different predictions of how priming from recent stimulus processing could interact with intended selection. The present experiment examined the interaction between exogenous attention and endogenous priming across trial sequences. A sound cue directed attention to left, right or both sides before a dichotic syllable pair was presented. Participants were asked to report one syllable from each trial. Results showed that responses were slower on trials where one of the presented syllables had also been presented on the previous trial. Within these trials, the repeated syllable was selected less frequently, and the responses doing so were slower. Examined according to response choice on the preceding trial, syllables that had been ignored on the preceding trial tended to be ignored on the current trial (negative priming), while syllables that had been selected on the preceding trial tended to be selected on the current trial (positive priming). Responses that followed these selection biases were faster than responses that did not. Response selection was also influenced by the attention direction cue for the current trial, but not by the cue presented on the preceding trial. The results support an attentional model where traces from the preceding processing are retained, and current selection is biased to minimize cognitive conflict between recent and current processing. Negative priming appears to be due to after-effects of preceding processing, independently of the intentions behind that processing. The study accounts for positive and negative priming of dichotic listening sequences within an established, computationally viable biased competition framework.     

On the transmission of partial information: inferences from movement-related brain potentials.

Results are reported from a new paradigm that uses movement-related brain potentials to detect response preparation based on partial information. The paradigm uses a hybrid choice-reaction go/nogo procedure in which decisions about response hand and whether to respond are based on separate stimulus attributes. A lateral asymmetry in the movement-related brain potential was found on nogo trials without overt movement. The direction of this asymmetry depended primarily on the signaled response hand rather than on properties of the stimulus. When the asymmetry first appeared was influenced by the time required to select the signaled hand, and when it began to differ on go and nogo trials was influenced by the time to decide whether to respond. These findings indicate that both stimulus attributes were processed in parallel and that the asymmetry reflected preparation of the response hand that began before the go/nogo decision was completed.     

A computational model of anterior cingulate function in speeded response tasks: effects of frequency,sequence, and conflict

A growing body of evidence from functional neuroimaging and computational modeling studies indicates that the anterior cingulate cortex (ACC) detects the presence of response conflict and conveys this information to other brain regions, enabling subsequent adjustments in cognitive control. The present study examined previous empirical findings of increased ACC for low-frequency stimuli across three distinct speeded response tasks (two-alternative forced choice, go/no-go, and oddball). Simulations conducted in a neural network model incorporating sequential priming mechanisms (developed in Cho et al., 2002) confirmed that a computational measure of response conflict was higher on low-frequency trials across all three tasks. In addition, the model captured detailed aspects of behavioral reaction time and accuracy data, predicted the dynamics of ACC activity related to trial sequence effects, and provided evidence for the functional role of conflict information in performance monitoring and optimization. The results indicate that the conflict-monitoring hypothesis, augmented by mechanisms for encoding stimulus history, can explain key phenomena associated with performance in sequential speeded response tasks.     

The locus and modulation of the location negative priming effect

Responding to the location of a target is slower when it appears at a recent distractor location [ignored-repetition (IR) trial] than when it arises at a new position [control (CO) trial], defining the location negative priming (NP) effect. On IR trials, both the distractor location and response are from the prior trial, and the locus question asks whether the delayed responding that arises is caused by the reused distractor position (i.e., a location locus) or the need to execute a distractor output (i.e., a response locus). A location NP procedure was used, incorporating a many:1 location-to-response mapping design, along with a response cue on some trials. A response locus for the location NP effect was indicated. Distractor-turned-target responses took longer to initiate than new outputs (many:1 paradigm), and valid response cues reduced distractor response interference and the location NP effect. Importantly, a possible S-R compatibility problem within the many:1 S-R paradigm was not supported.     

An examination of attentional control in the auditory modality: Further evidence for auditory orienting

Four experiments are reported that examine attentional control in the auditory modality. In Experiment 1, the subjects made detection responses to the onset of a monaurally presented pure tone that was preceded by a pure-tone cue. On a valid trial, the cue was presented in the same ear as the target; on an invalid trial, it was presented in the contralateral ear to the target; and on a neutral trial, it was presented in both ears. Overall performance was facilitated on valid trials in comparison with invalid trials. In later experiments, the subjects made choice decisions about the location of the target, and significant cuing effects were found relative to the neutral condition. Finally, performance was assessed in the presence of central (spoken) word cues. Here, the content of the cue specified the likely location of the target. Under these conditions, costs and benefits were found over a range of cue-target stimulus onset asynchronies. The results are discussed in terms of automatic and controlled attentional processes.     

Effects of stimulus-stimulus compatibility and stimulus-response compatibility on response inhibition

Previous studies demonstrated that interference control in stimulus–stimulus compatibility tasks slowed down stopping in the stop signal task (e.g., Kramer, A. F., Humphrey, D. G., Larish, J. F., Logan, G. D., & Strayer, D. L. (1994). Aging and inhibition: beyond a unitary view of inhibitory processing in attention. psychology and aging, 9, 491–512). In the present study, the impact of stimulus–stimulus compatibility and stimulus–response compatibility on response inhibition is further investigated. In Experiment 1, the stop signal task was combined with a traditional horizontal Simon task and with a vertical variant. For both dimensions, stopping responses was prolonged in incompatible trials, but only when the previous trial was compatible. In Experiment 2, the Simon task was combined with a spatial Stroop task in order to compare the effects of stimulus–stimulus and stimulus–response compatibility. The results demonstrated that both types of compatibility influenced stopping in a similar way. These findings are in favor of the hypothesis that response inhibition in the stop signal task and interference control in conflict tasks rely on similar mechanisms.