The effect of fMRI (noise) on cognitive control

Stressful situations, the aversiveness of events, or increases in task difficulty (e.g., conflict) have repeatedly been shown to be capable of triggering attentional control adjustments. In the present study we tested whether the particularity of an fMRI testing environment (i.e., EPI noise) might result in such increases of the cognitive control exerted. We found that participants were more effective in controlling episodic retrieval of previous stimulus-response bindings (Experiment 1), in switching to a new task (Experiment 2), and shielding a current goal from distracting response tendencies (Experiment 3) if they were exposed to challenging task situations, such as 70 dB echo planar imaging noise sampled from an fMRI scanner. These findings have considerable theoretical implications in questioning the widespread assumption that people are equally devoted to easy and more challenging tasks, and methodological implications in raising the possibility that experiments carried out in fMRI scanners or under otherwise challenging conditions systematically overestimate contributions from cognitive control processes.     

Anxiety Influences the Perceptual-Motor Calibration of Visually Guided Braking to Avoid Collisions

We investigated whether anxiety influences perceptual-motor calibration in a braking to avoid a collision task. Participants performed either a discrete braking task (Experiment 1) or a continuous braking task (Experiment 2), with the goal of stopping before colliding with a stop sign. Half of participants performed the braking task after an anxiety induction. We investigated whether anxiety reduced the frequency of crashing and if it influenced the calibration of perception (visual information) and action (brake pressure) dynamically between-trials in Experiment 1 and within-trials in Experiment 2. In the discrete braking task, anxious participants crashed less often and made larger corrective adjustments trial-to-trial after crashing, suggesting that the influence of anxiety on behavior did not occur uniformly, but rather dynamically with anxiety amplifying the reaction to previous crashes. However, when performing continuous braking, anxious participants crashed more often, and their within-trial adjustments of deceleration were less related to visual information compared to controls. Taken together, these findings suggest that the timescale and nature of the task mediates the influence of anxiety on the performance of goal-directed actions.     

Processing speed and mental retardation: Deadline procedures indicate fixed and adjustable limitations

Brewer and Smith (1984) showed that control mechanisms mediating speed-accuracy regulation contribute to retarded-nonretarded differences in processing speed, with poorly controlled trial-to-trial RT adjustments underlying the greater RT variability of retarded individuals. In Experiment 1, response deadlines controlled processing time, thus minimizing the influence of such control mechanisms. The obtained speed-accuracy relations showed that retarded subjects were unable to match nonretarded subjects' accuracy when responding as rapidly, thus indicating structural limitations on processing speed. The results of Experiment 2 showed, however, that significant adjustments to retarded subjects' processing speed--exceeding those produced by practice--are achievable. Extended training at a short deadline led to tighter control of RT adjustments, with substantial improvements in mean RT when subjects transferred to a self-paced RT task.     

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.     

The effect of interference in the early processing stages on response inhibition in the stop signal task

In the present study, the relation between interference at the early processing stages and response inhibition was investigated. In previous studies, response stopping appeared to be slowed down when irrelevant distracting information was presented. The purpose of the present study was to further explore the relationship between interference control and response inhibition. In Experiment 1, a stop signal paradigm was combined with a global/local task. The typical global-to-local interference effect is generally attributed to early processing stages, such as stimulus perception and identification. Results of this experiment demonstrated a congruency effect for both reaction time data and zstopping performance. In Experiment 2, these results were replicated with a flanker task that used stimulus-incongruent but response-congruent flankers. Results of both experiments suggest that response inhibition and interference at the early processing stages interact.     

The effect of interference in the early processing stages on response inhibition in the stop signal task

In the present study, the relation between interference at the early processing stages and response inhibition was investigated. In previous studies, response stopping appeared to be slowed down when irrelevant distracting information was presented. The purpose of the present study was to further explore the relationship between interference control and response inhibition. In Experiment 1, a stop signal paradigm was combined with a global/local task. The typical global-to-local interference effect is generally attributed to early processing stages, such as stimulus perception and identification. Results of this experiment demonstrated a congruency effect for both reaction time data and zstopping performance. In Experiment 2, these results were replicated with a flanker task that used stimulus-incongruent but response-congruent flankers. Results of both experiments suggest that response inhibition and interference at the early processing stages interact.     

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.     

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.     

Response force in RT tasks: Isolating effects of stimulus probability and response probability

Mattes, UIrich, and Miller (1997) found that as response probability decreases in a simple reaction time (RT) task, participants produce more forceful responses as well as longer RTs, suggesting a direct influence of preparatory processes on the motor system. In this previous study, however, response probability was confounded with stimulus probability, leaving open the possibility that response force was sensitive to stimulus- rather than response-related preparation. The present study was conducted to unravel the effects of stimulus and response probability. Experiment 1 manipulated stimulus probability and revealed that responses to a more probable stimulus are less forceful than responses to a less probable stimulus even when both stimuli require the same response. Experiment 2 demonstrated that this stimulus probability effect does not depend on the overall level of response probability. Experiment 3 showed an analogous effect for response probability when stimulus probability is kept constant. The complete pattern of results suggests that both stimulus probability and response probability affect the forcefulness of a response. It is argued that response probability exerts adirect influence on the motor system, whereas stimulus probability influences the motor system indirectly via premotoric adjustments.     

Inhibiting prepared and ongoing responses: Is there more than one kind of stopping?

Inhibiting movements has been investigated widely using the countermanding (stop signal) paradigm. Although it has been assumed that response inhibition, as measured by the countermanding task, generalizes to all forms of stopping, this has never been tested. In the present study, stopping performance in the countermanding paradigm was compared with stopping performance in a new paradigm in which a continuous-tracking task was used. Although stimulus presentations were matched across paradigms, the two tasks differed in the type of stopping required. In the countermanding paradigm, response inhibition latency was measured prior to response execution-this is, it was inferred from the successful withholding of a go response. In the new paradigm, response inhibition was carried out after response execution-that is, it was measured as the time to begin stopping a continuous tracking response. Results indicated that stopping latencies between the two paradigms were highly correlated, providing strong evidence that stopping an unexecuted response engages the same mechanisms as stopping an ongoing response.     

Reach tracking reveals dissociable processes underlying inhibitory control in 5‐ to 10‐year‐olds and adults

Researchers have proposed that two processes featuring distinct types of inhibition support inhibitory control: a response threshold adjustment process involving the global inhibition of motor output and a conflict resolution process involving competitive inhibition among co‐active response alternatives. To target the development of these processes, we measured the reaching behavior of 5‐ to 10‐year‐olds (Experiment 1) and adults (Experiment 2) as they performed an Eriksen flanker task. This method provided two key measures: initiation time (the time elapsed between stimulus onset and movement onset) and reach curvature (the degree to which a movement deviates from a direct path to the selected target). We suggest that initiation time reflects the response threshold adjustment process by indexing the degree of motoric stopping experienced before a movement is started, while reach curvature reflects the conflict resolution process by indexing the degree of co‐activation between response alternatives over the course of a movement. Our results support this claim, revealing different patterns effects in initiation time and curvature, and divergent developmental trajectories between childhood and adulthood. These findings provide behavioral evidence for the dissociation between global and competitive inhibition, and offer new insight into the development of inhibitory control.     

Impact of contingency manipulations on accessory stimulus effects

Accessory tone stimuli facilitate response performance despite being irrelevant for the current task. In order to investigate which processes are affected by accessory stimuli, we presented accessory tones in a simple response time (RT) task while varying the contingencies between accessory stimulation and either responses(Experiment 1) or stimulus conditions (Experiment 2). Accessory tones speeded up responding to a larger degree when they were conjointly presented within go compared with no-go trials. In contrast, contingency variation with stimulus conditions did not alter the impact of accessory stimuli. Additionally, accessory tones increased response force. Thus, we conclude that in simple RT tasks accessory tones influence response-related stages such as response selection and response execution rather than perceptual processes.     

Predictability influences stopping and response control

Using a continuous tracking task, the authors examined whether stopping is resistant to expectancies as well as whether it is a representative measure of response control. Participants controlled the speed of a moving marker by continuously adjusting their response force. Participants stopped their ongoing tracking in response to auditory signals on 25%, 50%, 75%, or 100% of trials. Stopping was contrasted with accelerating, in which participants accelerated the marker in response to the signals. In Experiment 1, on each trial participants either stopped or accelerated, allowing a trade-off between the two. In Experiments 2 and 3, participants only stopped or only accelerated, thus decreasing the likelihood of a trade-off. When a trade-off was possible, stopping was resistant to expectancies. However, with little or no trade-off, expectancies influenced stopping and accelerating similarly. These findings contrast with the established view that stopping is insensitive to expectancies. In addition, when trade-offs are prevented, these results confirm that stopping is representative of other response adjustment measures.     

Compatibility effects in stopping and response initiation in a continuous tracking task

Two experiments explored stopping performance using a new stimulus-response compatibility effect spanning action initiation and stopping. Participants tracked a sometimes-moving, sometimes-stationary target by controlling the speed of a response marker via a force sensor. In the compatible condition, participants pressed the sensor in response to the target moving and stopped pressing in response to the target stopping. In the incompatible condition, participants stopped pressing in response to the target moving and initiated pressing in response to the target stopping. Response initiation and stopping were found to be faster under compatible than under incompatible conditions, regardless of whether compatible and incompatible trials were blocked or mixed. These findings indicate that stopping, like response initiation, is influenced by stimulus-response properties such as compatibility. This in turn suggests that stopping is governed by constraints similar to those of other behaviours.     

Compatibility effects in stopping and response initiation in a continuous tracking task

Two experiments explored stopping performance using a new stimulus–response compatibility effect spanning action initiation and stopping. Participants tracked a sometimes-moving, sometimes-stationary target by controlling the speed of a response marker via a force sensor. In the compatible condition, participants pressed the sensor in response to the target moving and stopped pressing in response to the target stopping. In the incompatible condition, participants stopped pressing in response to the target moving and initiated pressing in response to the target stopping. Response initiation and stopping were found to be faster under compatible than under incompatible conditions, regardless of whether compatible and incompatible trials were blocked or mixed. These findings indicate that stopping, like response initiation, is influenced by stimulus–response properties such as compatibility. This in turn suggests that stopping is governed by constraints similar to those of other behaviours.     

Self-enhancement and theory-based correction processes

Two studies examined bias correction by manipulating a perceived chronic judgmental bias (i.e., overestimator/underestimator) using a modified dot estimation task. In Experiment 1, participants corrected for this perceived estimation bias by making adjustments away from the arbitrary feedback about their personal bias tendencies. In Experiment 2, the perceived desirability of the same estimation bias was manipulated. Results indicated that self-enhancement concerns impacted perceivers’ motivation to correct, at a cost to accuracy. These studies expand our current understanding of theory-based correction by including self-enhancement motives as causes of correction, demonstrating that such corrections can decrease rather than increase judgment accuracy, and illustrating the usefulness of a new perceived bias manipulation in theory testing.     

Early-extinction effects on a force response of humans

Humans were used to investigate changes in response force occurring soon after reinforcement was eliminated. In Experiment 1, in a 300-s baseline phase, 10 participants received a point for holding down a pressure sensor set to operate at a force equal to 85% of the maximum force the participants exerted during a pretest. Following this, during a 600-s extinction phase, criterion responses had no consequence. In Experiment 2, 6 participants worked on the same task, but (a) points were exchangeable for money and (b) after extinction, the reinforcement baseline phase was reinstated. In Experiment 3, 6 participants completed the same task as in Experiment 2, but the required minimum force was 60% of the maximum force exerted during the pretest. In each experiment, increases in response force relative to the mean and peak force exerted during the last 100 s of baseline were observed in most participants when force responses were aggregated into short sample intervals, but less so with longer ones. The increases, however, were not systematic across or within participants, questioning the generality of and the criteria for demonstrating an extinction burst.     

A goal activation approach to the study of executive function: an application to antisaccade tasks

We argue that a general control process, responsible for the activation and maintenance of task goals, is central to the concept of executive function. Failures of this process can become manifest as goal neglect: disregard of a task requirement even though it has been understood (Duncan, 1995). We discuss the results of several published and new experiments using various versions of the antisaccade task in order to investigate the circumstances under which goal neglect is likely to occur. Potentially conflicting results in the literature on adaptive control of saccadic eye movements are argued to be attributable to the extent to which different task versions elicit goal neglect. The results suggest an increased susceptibility to goal neglect of high-functioning older adults (Experiment 1) and of first-episode schizophrenia patients (Experiment 2), but not of patients with obsessive-compulsive disorder (Experiment 3). However, the degree to which such differences in susceptibility become manifest in task performance, is shown to be strongly influenced by manipulations of the relative saliency of task requirements. Theoretical and methodological implications for the study of executive function are discussed.     

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.     

Judgment and action knowledge in speed adjustment tasks: experiments in a virtual environment

Two experiments were conducted to investigate children's and adults’ knowledge of time and speed in action and judgment tasks. Participants had to set the speed of a moving car to a new speed so that it would reach a target line at the same time as a reference car moving at a higher speed and disappearing in a tunnel at the midway point. In Experiment 1 (24 10‐year‐olds, 24 adults), children's and adults’ speed adjustments followed the normative pattern when responses had to be graded linearly as a function of the car's initial speed. In a non‐linear condition, only adults’ action responses corresponded with the normative function. Simplifying the task by shortening the tunnel systematically in Experiment 2 (24 10‐year‐olds, 24 adults) enabled children to grade the speeds adequately in the action conditions only. Adults now produced normative response patterns in both judgment and action. Whether people show linearization biases was thus shown to depend on the interaction of age, task demands and response mode.