Cardiac activity in a simple reaction time task

Twenty subjects, half having high extraversion and the other half having low extraversion scores on the Eysenck Personality Inventory, performed a simple reaction time task in which the warning stimulus was a light and the imperative stimulus was a tone. Beat-by-beat analysis showed significantly different response patterns between the two groups in time of onset, magnitude, and duration of the cardiac responses. The extraversion measures were found to relate to central-nervous-system-strength types and to indicate relative strength of central inhibitory processes, as reflected by cardiac activity.     

Cardiac-somatic changes during a simple reaction time task: A developmental study

The relationship during a simple reaction time task between heart rate and four measures of task irrelevant somatic activity was evaluated in four age groups of children, i.e., 4-, 5-, 8-, and 10-year-olds and young adults, in order to evaluate further a hypothesized coupling of cardiac and somatic activity. At all age levels, phasic decreases in both heart rate and somatic activity coincident with performance were found with the magnitude of the effect increasing with age only on three somatic measures. However, tonic levels of both heart rate and somatic activity decreased with age. Performance on the reaction task was found to be inversely related to the age-related phasic somatic effects as well as age-related tonic heart rate and somatic activity.     

A free, easy-to-use, computer-based simple and four-choice reaction time programme: the Deary-Liewald reaction time task

Reaction time tasks are used widely in basic and applied psychology. There is a need for an easy-to-use, freely available programme that can run simple and choice reaction time tasks with no special software. We report the development of, and make available, the Deary-Liewald reaction time task. It is initially tested here on 150 participants, aged from 18 to 80, alongside another widely used reaction time device and tests of fluid and crystallised intelligence and processing speed. The new task’s parameters perform as expected with respect to age and intelligence differences. The new task’s parameters are reliable, and have very high correlations with the existing task. We also provide instructions for downloading and using the new reaction time programme, and we encourage other researchers to use it.     

Comparisons of reaction time patterns in a sequential visual recognition task with simple geometric forms

Right isosceles triangles, which differed in size and orientation, were presented in a sequential visual recognition task. Subjects produced an identity match response if the first self-presented stimulus, now in memory, was identical to a sequentially presented stimulus and a nonidentity match response if the subsequently presented stimulus differed in either or both size and orientation. The pattern of nonidentity recognition reaction times produced was compared to predicted patterns deduced from several theories of form information processing. The pattern of responses for both group and individual data were better described by serial and parallel self-terminating models with probabilistic assumptions than they were by template or deterministic serial or parallel models. A second study, in which identity and nonidentity response bias was equated, found that the identity responses were significantly faster than nonidentity responses, supporting wholistic processing for the identity matches and, when combined with the nonidentity match results, supporting a dual process theory.     

The influence of temporal factors on automatic priming and conscious expectancy in a simple reaction time task

In a previous study, we reported a dissociation between subjective expectancy and motor behaviour in a simple associative learning task (Perruchet, Cleeremans, & Destrebecqz, 2006). According to previous conditioning studies (Clark, Manns, & Squire, 2001), this dissociation is observed when the to-be-associated events coterminate and thus overlap in time (a training regimen called delay conditioning), but not when they are separated by a temporal delay (trace conditioning). In this latter situation indeed, there tends to be a direct relationship between subjective expectancy and behaviour. In this study, we further investigated this issue in a series of experiments where conscious and unconscious components of performance were pitted against each other. In Experiments 1–3, participants performed a simple reaction time task in which a preparatory signal (a tone) either overlapped with or terminated earlier than the imperative stimulus (a visual target presented in 50% of the trials). After each response, participants also had to state how much they expected the imperative stimulus to be displayed on the next trial. Results indicate that reaction times tend to decrease when the tone is consistently followed by the visual target across successive trials, whereas conscious expectancy for the target decreases at the same time. Importantly, we systematically found that the temporal relationship between the tone and the target failed to influence performance. In a fourth experiment, we examined whether these results extend to a two-choice reaction time task. To our surprise, we observed a direct relationship between subjective expectancies and reaction time in that situation. We nevertheless observed that the introduction of a delay between the tone and the target had, once again, no effect on performance.     

Wavelength effects on simple reaction time

Simple reaction time was measured to spectral lights matched photometrically in luminance. When these lights were presented on a dimmer achromatic background, reaction time did not vary as a function of wavelength. Moreover, reaction times to white and chromatic lights were the same. When the luminance of the background was the same as that of the chromatic lights, reaction time increased and showed a strong effect of wavelength. Reaction time in this condition appeared to follow a saturation function. The results are described in terms of the operation of achromatic and chromatic processing channels.     

Effects of stimulus probability on reaction time in a number-naming task

Subjects were required to respond to the visual presentation of numerals by uttering syllables closely resembling the names of the numerals. Information in stimulus ensembles was varied by manipulating the number of alternative stimulus configurations that could appear, the relative frequencies of stimuli within an ensemble and the probability of a response being required. An increasing linear function was a good first approximation to the relation between reaction time and information transmission. Systematic deviations from this function were found and an attempt is made to explain them by introducing an intervening variable, “effective probability.”     

Psychological distance and reaction time in a Stroop task

Several sources of interference may simultaneously affect the onset of the well-known “Stroop effect.” Among them is the semantic component, which is reflected in the gradient or semantic effect. This effect consists of an increase in the amount of interference as the semantic distance between the word and the color concept decreases. Shepard (Science 237:1317–1323, 1987) relates psychological space, measured through multidimensional scaling, to mean response times. The present investigation aims to study the function relating the semantic gradient with the psychological distance between the word and the color in a Stroop task. After measuring the gradient, we obtained the subjective rating of the degree of dissimilarity of the gradient words with the concept of “color.” In our work, we show that the amount of interference in a Stroop task increases when the semantic distance from the word to the color concept decreases, and it does so exponentially. We replicated the study with different stimuli to test the robustness of the results.     

One night of sleep deprivation affects reaction time, but not interference or facilitation in a Stroop task

The Stroop color-naming task is one of the most widely studied tasks involving the inhibition of a prepotent response, regarded as an executive function. Several studies have examined performance on versions of the Stroop task under conditions of acute sleep deprivation. Though these studies revealed effects on Stroop performance, the results often do not differentiate between general effects of sleep deprivation on performance and effects specifically on interference in the Stroop task. To examine the effect of prolonged wakefulness on performance on the Stroop task, we studied participants in a 40-h "constant routine" protocol during which they remained awake in constant conditions and performed a Stroop color-naming task every two hours. We found that reaction time was slowest when the color and word did not match (incongruent), fastest when the color and word did match (congruent), and intermediate when participants named the color of the non-word stimulus (neutral). Performance on all three trial types degraded significantly as a function of time awake. Extended wakefulness did not significantly change the additional time needed to respond when the color and word did not match (Stroop interference), nor did it change the amount of facilitation when color and word matched. These results indicate that one night of sleep deprivation influences performance on the Stroop task by an overall increase in response time, but does not appear to impact the underlying processes of interference or facilitation. The results suggest that the degree to which an "executive function" is affected by sleep deprivation may depend on the particular executive function studied and the degree to which it is subserved by the prefrontal cortex.     

The effects of aging on reaction time in a signal detection task

The effects of aging on response time are examined in 2 simple signal detection tasks with young and older subjects (age 60 years and older). Older subjects were generally slower than young subjects, and standard Brinley plot analyses of response times showed typical results: slopes greater than 1 and (mostly) negative intercepts. R. Ratcliff, D. Spieler, and G. McKoon (2000) showed that the slopes of Brinley plots measure the relative standard deviations of the distributions of response times for older versus young subjects. Applying R. Ratcliff's (1978) diffusion model to fit the response times, their distributions, and response accuracy, it was found that the larger spread in older subjects' response times and their slowness relative to young subjects comes from a 50-ms slowing of the nondecision components of response time and more from conservative settings of response criteria.     

The time course of attention in a simple auditory detection task

What is the time course of human attention in a simple auditory detection task? To investigate this question, we determined the detectability of a 20-msec, 1000-Hz tone presented at expected and unexpected times. Twelve listeners who expected the tone to occur at a specific time after a 300-msec narrowband noise rarely detected signals presented 150-375 msec before or 100-200 msec after that expected time. The shape of this temporal-attention window depended on the expected presentation time of the tone and the temporal markers available in the trials. Further, though expecting the signal to occur in silence, listeners often detected signals presented at unexpected times during the noise. Combined with previous data, these results further clarify the listening strategy humans use when trying to detect an expected sound: Humans seem to listen specifically for that sound, while ignoring the background in which it is presented, around the time when the sound is expected to occur.     

Effector-related sequence learning in a bimanual-bisequential serial reaction time task

In a bimanual-bisequential version of the serial reaction time (SRT) task participants performed two uncorrelated key-press sequences simultaneously, one with fingers of the left hand and the other with fingers of the right hand. Participants responded to location-based imperative stimuli. When two such stimuli appeared in each trial, the results suggest independent learning of the two sequences and the occurrence of intermanual transfer. Following extended practice in Experiment 2, transfer of acquired sequence knowledge was not complete. Also in Experiment 2, when only one stimulus appeared in each trial specifying the responses for both hands so that there was no basis for separate stimulus-stimulus or separate response-effect learning, independent sequence learning was again evident, but there was no intermanual transfer at all. These findings suggest the existence of two mechanisms of sequence learning, one hand-related stimulus-based and the other motor-based, with only the former allowing for intermanual transfer.     

Initiation of bilateral responses in a kinesthetic reaction time task

Two experiments are presented in which different mechanisms controlling each limb in a bilateral arm response to a unilateral kinesthetic stimulus are postulated to occur. In Experiment 1, the limb serving as the stimulus are postulated to occur. In Experiment 1, the limb serving as the stimulus limb was described as operating with relative invariance by using a tightly coupled input-output reflexive pathway, whereas the nonstimulus limb appeared to be controlled by higher-order processing thought to be more susceptible to influences such as hemispheric specialization and stimulus expectancy. The differential control model was further tested in Experiment 2 by retaining the interhemispheric pathway of the unilateral kinesthetic stimulus but experimentally uncoupling the reflex mechanism from the stimulus side. Analyses of bilateral EMG premotor latencies under these conditions revealed that each response side can be controlled at separate levels-i.e., by a reflexive type mechanism or by higher-order processing when one of the response limbs is also the stimulus limb, both sides reflect behavior that is best described by an information processing type of voluntary control.     

Assessment of sexual preference using a choice reaction time task

The purpose of this study was to investigate the use of a choice reaction time task, during which slides of sexually explicit and neutral stimuli were used as an interference task, to differentiate between groups of individuals on the basis of their sexual preference. Twenty subjects, in each of the four groups (heterosexual males, heterosexual females, homosexual males, and homosexual females), participated in this study. Sexual orientation was determined by self-report. Subjects were given a choice reaction time with interference task, followed by a recall incidental learning task. A significant higher-order interaction was found among gender, orientation, and stimulus type for all four groups. This interaction indicated a longer reaction time to slides depicting preferred sexual partners than to nonpreferred sexual partners or neutral scenes. These results indicate that sexual arousal does interfere with cognitive processing. A main effect for gender was found for the incidental learning task, with males having the fewest errors.