Response Conflict Determines Sequential Effects in Serial Response Time Tasks With Short Response-Stimulus Intervals.

Author(s):  
Ines Jentzsch ◽  
Hartmut Leuthold
Author(s):  
Nabil Hasshim ◽  
Michelle Downes ◽  
Sarah Bate ◽  
Benjamin A. Parris

Abstract. Previous analyses of response time distributions have shown that the Stroop effect is observed in the mode (μ) and standard deviation (σ) of the normal part of the distribution, as well as its tail (τ). Specifically, interference related to semantic and response processes has been suggested to specifically affect the mode and tail, respectively. However, only one study in the literature has directly manipulated semantic interference, and none manipulating response interference. The present research aims to address this gap by manipulating both semantic and response interference in a manual response Stroop task, and examining how these components of Stroop interference affect the response time distribution. Ex-Gaussian analysis showed both semantic and response conflict to only affect τ. Analyzing the distribution by rank-ordered response times (Vincentizing) showed converging results as the magnitude of both semantic and response conflict increased with slower response times. Additionally, response conflict appeared earlier on the distribution compared to semantic conflict. These findings further highlight the difficulty in attributing specific psychological processes to different parameters (i.e., μ, σ, and τ). The effect of different response modalities on the makeup of Stroop interference is also discussed.


1989 ◽  
Vol 41 (1) ◽  
pp. 47-62 ◽  
Author(s):  
E. A. Maylor ◽  
P. M. A. Rabbitt

It is known that alcohol increases the time taken to identify signals and to make responses to them, but it is not known whether it also slows the rate of preparation for such events. These two performance parameters are not necessarily related, as age affects the former but not the latter. Twenty subjects participated in a 4-choice reaction time experiment in which they received no alcohol (NA) in the first session and either no alcohol (10 subjects) or 0.8 ml alcohol (A) per kg body weight (10 subjects) in the second session. In each session there were 300 practice trials, followed by 400 experimental trials at each one of five Response–Stimulus Intervals (RSI: 50, 100, 200, 400, and 800 msec). There was a significant effect of alcohol such that the reduction in response time from the first to the second session was 39 msec larger for the NA/NA group than for the NA/A group. Response time decreased significantly with increasing RSI, but there was no interaction between the effect of alcohol and RSI. Thus, alcohol slows the processing of an event requiring a choice response; however, like age and individual differences, but unlike practice, alcohol has no effect on the rate of preparation for that event. In addition, an analysis of what happened before and after an error revealed that practice and increasing RSI produce real improvements in performance rather than shifts in the tradeoff between speed and accuracy, whereas alcohol produces a real impairment. It is concluded that the relationship between the rate of preparation for, and processing of, a stimulus is not simple, as one factor (practice) influences both rates, whereas other factors (alcohol, individual differences, and age) influence the rate of processing only.


1978 ◽  
Vol 21 (4) ◽  
pp. 768-778 ◽  
Author(s):  
Stephen C. McFarlane ◽  
David Prins

Neural response time (NRT) was compared for 12 adult stutterers and 12 matched normal speakers on two verbal tasks (production of /pæ/ and /bæ/) and one oral, nonverbal task (lip closure) in response to visual and auditory stimulation. The auditory response stimulus was presented separately to the left and right ears, and the visual stimulus to both eyes. NRT was defined as the time interval between stimulus offset and the onset of electromyographic (EMG) activity from orbicularis oris superior muscle. Results show, in general, that stutterers are slower in NRT for all response tasks in both stimulus modes. Significant differences were found, however, for only the auditory mode. Analyses of the differences between and within groups for response tasks and stimulus modes are discussed in terms of recent research in and theory of timing disturbances in stuttering.


2020 ◽  
Vol 74 (1) ◽  
pp. 77-94 ◽  
Author(s):  
Victoria KE Bart ◽  
Iring Koch ◽  
Martina Rieger

During motor imagery, global inhibition and effector-specific inhibition contribute to prevent actual movements. We investigated the decay of inhibition using an action-mode switching paradigm. Participants switched between imagined and executed hand movements. Response–stimulus intervals (RSIs) were varied (200, 700, 1,300, and 2,000 ms). As inhibition (due to imagination) or activation (due to execution) in one trial affects performance in the subsequent trial, we analysed sequential effects. Evidence for the contribution of global inhibition (e.g., switch benefits in execution [E]—imagination [I] sequences compared with I-I sequences) and effector-specific inhibition (e.g., hand repetition costs after an imagination trial) was observed. Sequential effects decreased with increasing RSIs, indicating that both forms of inhibition are subject to decay. However, the decrease of sequential effects was less pronounced for global inhibition than for effector-specific inhibition. This indicates that global inhibition may decay slowly, whereas effector-specific inhibition decays rather quickly. In conclusion, global inhibition may be at least partly implemented in all contexts in which motor imagery has to be performed, whereas effector-specific inhibition may contribute to motor imagery only as soon as the exact movement parameters are known and may decay quickly after the imagined movement has been performed.


2013 ◽  
Vol 120 (3) ◽  
pp. 628-666 ◽  
Author(s):  
Matt Jones ◽  
Tim Curran ◽  
Michael C. Mozer ◽  
Matthew H. Wilder

2004 ◽  
Vol 14 (02) ◽  
pp. 667-678 ◽  
Author(s):  
INES JENTZSCH

Human performance is strongly influenced by the sequence of events. Decreasing the response-stimulus interval (RSI) between events qualitatively changes these so-called sequential effects. Using event-related brain potentials (ERPs) to detect electrical brain activity related to sequential patterns helps to uncover mechanisms underlying the observed performance data. Using a spatial compatible two-choice task ERPs were recorded from 32 electrode sites and Independent Component Analysis (ICA) applied to separate sequence-sensitive ERP components from two experiments, involving different RSIs. Independent Component Analysis was able to separate temporally and spatially overlapping ERP components. Sensitivity to the sequence of preceding events could be revealed in an early subcomponent of the N100 complex. Moreover, and in line with earlier reports sequential effects were also observed in P300 subcomponents.


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