The Time Course of Preparation*

1967 ◽  
Vol 19 (3) ◽  
pp. 272-279 ◽  
Author(s):  
Paul Bertelson
Keyword(s):  
Visual Stimulus ◽  
Refractory Period ◽  
Time Course ◽  
Reaction Times ◽  
Warning Signal ◽  
High Time ◽  
Refractory Periods ◽  
Time Uncertainty ◽  
Order Of Magnitude ◽  
Choice Reaction Times

The time course of the adjustments triggered by a warning signal was studied by measuring choice reaction times (RTs) at different predictable foreperiods after such a signal. Before the warning signal, a high time uncertainty situation was created by imposing either a long constant foreperiod of 5 sec. or one varying in the range 1.5 to 5 sec. The warning signal was a click. Foreperiods ranging from 0 to 300 millisec. were used in different blocks of trials. The stimulus was the onset of one of two lamps calling for the pressing of one of two keys. A control condition, without click, was used also. RTs were found to decrease continuously when the forperiod was increased from 0 to 100-150 millisec. The click delivered simultaneously with the stimulus permitted reactions significantly faster than in the control condition. It is concluded (a) that the latency of preparation can be much shorter than the 2 to 4 sec. reported by Woodrow; (b) that the warning signal can be used as a time cue to start preparatory adjustments without starting a refractory period of the order of magnitude found in experiments with pairs of successive reactions, and thus that such refractory periods are not the inevitable cost of paying attention to a signal. There is also some suggestion that in this situation the click not only triggers preparatory adjustments, but also causes an immediate facilitation of the reaction to the visual stimulus.

scholarly journals Dissecting the inflammatory twitch in allergically inflamed mice

2016 ◽  
Vol 310 (10) ◽  
pp. L1003-L1009 ◽  
Author(s):  
Joshua J. Pothen ◽  
Matthew E. Poynter ◽  
Lennart K. A. Lundblad ◽  
Jason H. T. Bates
Keyword(s):  
Inflammatory Response ◽  
Refractory Period ◽  
Time Course ◽  
Lavage Fluid ◽  
Gm Csf ◽  
Refractory Periods ◽  
Sequence Of Events ◽  
Cell Counts ◽  
Airways Resistance ◽  
Predetermined Time

We have previously advanced the hypothesis that the allergic inflammatory response in the lungs occurs as a self-limited sequence of events that begins with the onset of inflammation and then resolves back to baseline over a predetermined time course (Pothen JJ, Poynter ME, Bates JH. J Immunol 190: 3510–3516, 2013). In the present study we tested a key prediction of this hypothesis, which is that the instigation of the allergic inflammatory response should be accompanied by a later refractory period during which the response cannot be reinitiated. We challenged groups of ovalbumin-sensitized BALB/c mice for 3, 14, 21 and 31 consecutive days with aerosolized ovalbumin. We measured airways responsiveness as well as cell counts and cytokines in bronchoalveolar lavage fluid after the final challenge in subgroups from each group. In other subgroups we performed the same measurements following rest periods and after a final single recall challenge with antigen. We determined that the refractory periods for GM-CSF, KC, and IL-5 are no longer than 10 days, while those for IFNγ and IL-10 are no longer than 28 days. The refractory periods for total leukocytes and neutrophils were no greater than 28 days, while that for eosinophils was more than 28 days. The refractory period for airways resistance was less than 17, while for lung elastance it was longer than 28 days. Our results thus demonstrate that the components of the allergic inflammatory response in the lung have finite refractory periods, with the refractory period of the entire response being in the order of a month.

The Psychological Refractory Period and Vertex Evoked Potentials

1972 ◽  
Vol 24 (2) ◽  
pp. 175-192 ◽  
Author(s):  
John Boddy
Keyword(s):  
Refractory Period ◽  
Time Course ◽  
Psychological Refractory Period ◽  
Single Channel ◽  
Random Sequence ◽  
Reaction Times ◽  
Central Processor ◽  
Sensory Evoked Potential ◽  
Sensory Evoked ◽  
Simple Rt

The averaged sensory evoked potential (EP) was recorded from the scalp (vertex to mastoid) in a psychological refractory period experiment in which 12 young adults participated. Reaction times (RTs) were measured to either both or only the second of pairs of stimuli, in different trial blocks, with inter-stimulus intervals (ISIs) of 100, 200, 300 and 400 msec occurring in random sequence. EPs were recorded at each ISI. No latency changes could be found in the prominent non-specific components (P1–N1–P2) of the EP to stimulus 2 even at ISIs where the RT was substantially delayed. Thus the notions that the RT2 delay is due to occupation of a single channel central processor by S1 and that non-specific EP components reflect the time course of information processing in underlying neural tissue, do not lend each other mutual support. Furthermore, as profound amplitude refractoriness in components P1–N1 and N1–P2 persisted at ISIs where RT was as fast or faster than simple RT, there appears to be a dissociation between “psychological refractoriness” and “physiological refractoriness”. The implications of these results are discussed.

Effect of Marihuana on the Psychological Refractory Period

1974 ◽  
Vol 38 (3) ◽  
pp. 959-962 ◽  
Author(s):  
Herbert Moskowitz ◽  
Richard Shea ◽  
Marcelline Burns
Keyword(s):  
Auditory Stimulus ◽  
Visual Stimulus ◽  
Refractory Period ◽  
Psychological Refractory Period ◽  
Reaction Times

Reaction times to an auditory stimulus (RT1) and a subsequent visual stimulus (RT2) were measured for 12 Ss under three levels of smoked marihuana. Marihuana impaired responses; effect was larger on RT2 than on RT1. However, delays of RT2 are longer than would be predicted in terms of the psychological refractory period.

Faster Choice-Reaction Times to Positive than to Negative Facial Expressions

2003 ◽  
Vol 17 (3) ◽  
pp. 113-123 ◽  
Author(s):  
Jukka M. Leppänen ◽  
Mirja Tenhunen ◽  
Jari K. Hietanen
Keyword(s):  
Facial Expressions ◽  
Cognitive Processing ◽  
Response Selection ◽  
Reaction Times ◽  
Happy Face ◽  
Response Onset ◽  
Response Execution ◽  
Onset Response ◽  
Positive Stimuli ◽  
Choice Reaction Times

Abstract Several studies have shown faster choice-reaction times to positive than to negative facial expressions. The present study examined whether this effect is exclusively due to faster cognitive processing of positive stimuli (i.e., processes leading up to, and including, response selection), or whether it also involves faster motor execution of the selected response. In two experiments, response selection (onset of the lateralized readiness potential, LRP) and response execution (LRP onset-response onset) times for positive (happy) and negative (disgusted/angry) faces were examined. Shorter response selection times for positive than for negative faces were found in both experiments but there was no difference in response execution times. Together, these results suggest that the happy-face advantage occurs primarily at premotoric processing stages. Implications that the happy-face advantage may reflect an interaction between emotional and cognitive factors are discussed.

scholarly journals Excessive Pressure in Multichambered Cuffs Used for Sequential Compression Therapy

2002 ◽  
Vol 82 (10) ◽  
pp. 1000-1008 ◽  
Author(s):  
Patrick Segers ◽  
Jean-Paul Belgrado ◽  
Andre Leduc ◽  
Olivier Leduc ◽  
Pascal Verdonck
Keyword(s):  
Time Course ◽  
Compression Therapy ◽  
Lymphatic Drainage ◽  
Chamber Pressure ◽  
Excessive Pressure ◽  
Ellipsoidal Model ◽  
Order Of Magnitude ◽  
Pneumatic Compression Devices ◽  
Target Pressure ◽  
The Relationship

Abstract Background and Purpose. Pneumatic compression devices, used as part of the therapeutic strategy for lymphatic drainage, often have cuffs with multiple chambers that are inflated sequentially. The purpose of this study was to investigate (1) the relationship between cuff chamber pressure (Pchamber) and the pressure on the cuff-skin interface (Pinterface) and (2) the mechanical interaction of cuff chambers and consequences for device control. Subjects and Methods. In this study, we used 3 cylindrical (60-, 80-, and 100-mm-diameter) model limbs and 1 ellipsoidal model of the arm to test a commercially available pressure controller using “target pressures,” indicated by the controller, of 30, 60, 80, and 100 mm Hg. We studied the time course of Pchamber and Pinterface during the inflation sequence and the effect of local curvature on Pinterface. Results. Our data indicated that, overall, Pinterface is of the same order of magnitude as Pchamber. There was some effect of model diameter and shape, with the smaller curvatures yielding the highest Pinterface. Cuff chamber interaction led to Pchamber and Pinterface values in the most distal (first inflated) chamber that were up to 80% higher than the target pressure. For the 80-mm cylindrical model, for instance, pressure in this chamber reached 54, 98, 121, and 141 mm Hg, respectively, instead of the 30, 60, 80, and 100 mm Hg indicated by the controller. Discussion and Conclusion. The discrepancy between the target pressure, indicated by the controller, and the pressure measured inside the cuff chambers undermines the therapeutic control and efficacy of the pneumatic compression devices. Because the measured pressures were far beyond the pressure level indicated by the controller, it is recommended that pneumatic compression devices be used at much lower target pressures (<30 mm Hg) than those applied in clinical practice.

The Effects of Ethyl Alcohol on a Driver's Driving Skill, Visual Perception, Risk Acceptance, Choice Reaction Times and Information Processing Rates

1974 ◽  
Vol 18 (2) ◽  
pp. 116-116
Author(s):  
Helmut T. Zwahlen
Keyword(s):  
Information Processing ◽  
Standard Deviation ◽  
Visual Perception ◽  
Reaction Times ◽  
Driving Skill ◽  
Alcohol Condition ◽  
The Mean ◽  
Risk Acceptance ◽  
Standard Deviations ◽  
Choice Reaction Times

Twelve subjects (20–37 years old) were tested in the laboratory and eleven out of these were also tested in a car in the field, first under a no alcohol condition and then under an alcohol condition (approximately 0.10% BAC). In the laboratory the subjects simple and choice reaction times for two uncertainty modes were measured and their information processing rates (3 bits unsertainty) were determined. In the field the subjects driving skill for driving through a gap with 20 inches total clearance at 20 MPH was measured, as well as their static visual perceptual capabilities and risk acceptance decisions for a 46 feet viewing distance using psychophysical experimental methods. Based upon the driving skill measure (standard deviation of centerline deviations in the gap), the mean of the psychometric visual gap perception function and the mean of the psychometric gap risk acceptance function, the “Safety Distance” and the “Driver Safety Index” (DSI) were obtained. Based upon a statistical analysis of the data we may conclude first that the effects of alcohol (approximately 0.10% BAC) vary widely from one subject to another (slighthly improved performance to highly impaired performance) and that the changes in the group averages of the means and standard deviations of the psychometric visual perception and risk acceptance functions, the driving skill distributions, the “Safety Distances” and the DSI's for the subjects (although all changes in the group averages are in the expected direction) are statistically not significant (α = .05). Second, the group average of the means of the choice reaction times for the subjects increased by 5% under the alcohol condition (statistically significant, α = .05), but more important the group average of the standard deviations of the choice reaction times for the subjects increased by 23% (statistically significant, α = .05). The group average of the information processing rates for the subjects decreased by 3% (statistically not significant, α = .05) under the alcohol condition. A system model in which the system demands on the driver are represented in terms of choice reaction times is used to demonstrate that the increase in performance variability (expressed by the standard deviation of choice reaction times) under the influence of alcohol provides a much better explanation for the higher accident involvement than the historically most frequently used rather small increase in average performance (expressed by the mean of choice reaction times).

scholarly journals Comparative analysis of reactions to visual and auditory stimuli in research on EEG evoked potentials

2018 ◽  
Vol 7 ◽  
pp. 172-177
Author(s):  
Łukasz Tyburcy ◽  
Małgorzata Plechawska-Wójcik
Keyword(s):  
Comparative Analysis ◽  
Evoked Potentials ◽  
Auditory Stimulus ◽  
Visual Stimulus ◽  
Visual Stimuli ◽  
Reaction Times ◽  
Auditory Stimuli

The paper describes results of comparison of reactions times to visual and auditory stimuli using EEG evoked potentials. Two experiments were used to applied. The first one explored reaction times to visual stimulus and the second one to auditory stimulus. After conducting an analysis of data, received results enable determining that visual stimuli evoke faster reactions than auditory stimuli.

Respiration-dependent Movements of the Column of Stylidium gvaminifolium

1981 ◽  
Vol 8 (1) ◽  
pp. 45 ◽  
Author(s):  
G.P Findlay ◽  
N Findlay
Keyword(s):  
Refractory Period ◽  
Angular Displacement ◽  
Metabolic Energy ◽  
Original Position ◽  
Firing Process ◽  
Mechanical Stimuli ◽  
Anaerobic Conditions ◽  
Absolute Refractory Period ◽  
Refractory Periods ◽  
Graded Responses

The column of the trigger plant, Stylidium graminifolium, when fully set responds to mechanical stimuli by flipping through an angle of about 4 radians in a fast firing movement lasting about 15-30 ms, and then slowly resetting to its original position in about 400 s. After resetting there is an absolute refractory period of about 500 s during which no further response to stimuli can be initiated, followed by a relative refractory period when graded responses increasing in rate and magnitude with time can be obtained. The resetting movement and the process, occurring during the refractory period, allowing subsequent firing to occur, are inhibited when the air surrounding the column is replaced by nitrogen. The firing movement, however, is not affected by these anaerobic conditions. Thus the firing movement is caused by passive physical forces, rapidly utilizing potential energy from a store built up during the previous resetting and refractory periods. Removal of the labellum, which the column touches when set, causes the column to oscillate with amplitude of about 3-3.5 radians and period of 1-2 ks. When the column is held at a constant angular displacement it develops an oscillatory torque with similar period. These oscillations are inhibited at all stages of the cycle by anaerobic conditions. It appears that the oscillatory behaviour is not a slowed-down firing process followed by normal resetting, but is linked throughout the cycle to the metabolic energy supply.

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