Millisecond interval timer and auditory reaction time programs for the IBM PC

Many types of behavioral research require the determination of elapsed time, for example to establish interstimulus intervals and to measure reaction time. The use of an IBM PC for on-line control of such applications is limited by the poor timing resolution ordinarily available. The IBM BIOS time information that is used for the BASIC TIMER function can result in interval timing errors as great as 110 msec. A machine language subroutine is described that can provide 1-msec accuracy. A BASIC program is also described that employs this subroutine to measure auditory reaction time.     

Measuring reaction time with millisecond accuracy using the TRS-80 microcomputer

A machine language subroutine is proposed for measuring reaction time with millisecond accuracy using the TRS-80 microcomputer. This timer is accurate to 1 msec in the first 30,000 msec and to 5 msec in the first 65,000 msec (1 part in 10,000).     

Measuring keyboard response delays by comparing keyboard and joystick inputs

The response characteristics of PC keyboards have to be identified when they are used as response devices in psychological experiments. In the past, the proposed method has been to check the characteristics independently by means of external measurement equipment. However, with the availability of different PC models and the rapid pace of model change, there is an urgent need for the development of convenient and accurate methods of checking. The method proposed here consists of raising the precision of the PC’s clock to the microsecond level and using a joystick connected to the MIDI terminal of a sound board to give the PC an independent timing function. Statistical processing of the data provided by this method makes it possible to estimate accurately the keyboard scanning interval time and the average keyboard delay time. The results showed that measured keyboard delay times varied from 11 to 73 msec, depending on the keyboard model, with most values being less than 30 msec.     

A simple method to record arm positioning movements in man with an Apple computer

This paper describes a simple method to record arm positioning movements in humans, via the game paddle entry of an Apple computer. A machine language subroutine reads the successive positions of a rotating potentiometer, with an angular accuracy of .5 deg and a time interval between two measures of 2.5 msec, and stores them sequentially in RAM memory. These measures can be retrieved for further computations of movement parameters.     

STEREO: A program to analyze stereotyped open field locomotion

In rats, amphetamine produces stereotyped locomotion which is characterized by perseverative movement along a fixed route around the perimeter of an open field. The program described in this paper is designed to facilitate analysis of stereotyped locomotion by measuring the repetitive nature of trips between adjacent quadrants of the apparatus using a method described by Mueller, Hollingsworth, and Cross (1989a) which subdivides locomotion into a series of trip lengths. The program is written in Microsoft QuickBASIC to run on an IBM PC/XT or compatible machine. Data from the program can be read by spreadsheets.     

STEREO: A program to analyze stereotyped open field locomotion

In rats, amphetamine produces stereotyped locomotion which is characterized by perseverative movement along a fixed route around the perimeter of an open field. The program described in this paper is designed to facilitate analysis of stereotyped locomotion by measuring the repetitive nature of trips between adjacent quadrants of the apparatus using a method described by Mueller, Hollingsworth, and Cross (1989a) which subdivides locomotion into a series of trip lengths. The program is written in Microsoft QuickBASIC to run on an IBM PC/XT or compatible machine. Data from the program can be read by spreadsheets.     

Discriminating time intervals presented in sequences marked by visual signals.

This article presents the results of three experiments on the discrimination of time intervals presented in sequences marked by brief visual signals. In Experiment 1A (continuous condition), the participants had to indicate whether, in a series of 2-4 intervals marked by 3-5 visual signals, the last interval was shorter or longer than the previous one(s). In Experiment 1B (discontinuous condition), the participants indicated whether, in a presentation of two series of 1-3 intervals, with each series being marked by 2-4 signals, the intervals of the second sequence were shorter or longer than those of the first. Whenever one, two, or three standard intervals were presented, the difference threshold was as high at 150 msec as it was at 300 msec with the continuous method but increased monotonically from 150 to 900 msec with the discontinuous method. With both methods, the increase was well described by Weber's law--the Weber fraction was roughly constant--between 600 and 900 msec (Experiment 2), whereas between 900 and 1,200 msec (Experiment 3), the Weber fraction increased.     

Discriminating time intervals presented in sequences marked by visual signals

This article presents the results of three experiments on the discrimination of time intervals presented in sequences marked by brief visual signals. In Experiment 1A (continuous condition), the participants had to indicate whether, in a series of 2–4 intervals marked by 3–5 visual signals, the last interval was shorter or longer than the previous one(s). In Experiment 1B (discontinuous condition), the participants indicated whether, in a presentation of two series of 1–3 intervals, with each series being marked by 2–4 signals, the intervals of the second sequence were shorter or longer than those of the first. Whenever one, two, or three standard intervals were presented, the difference threshold was as high at 150 msec as it was at 300 msec with the continuous method but increased monotonically from 150 to 900 msec with the discontinuous method. With both methods, the increase was well described by Weber’s law&#x2014the Weber fraction was roughly constant&#x2014between 600 and 900 msec (Experiment 2), whereas between 900 and 1,200 msec (Experiment 3), the Weber fraction increased.     

Suitability of the IBM XT,AT, and PS/2 keyboard,mouse, and game port as response devices in reaction time paradigms

The IBM PC keyboard is a convenient response panel for subjects in a reaction time task when the stimuli are presented on the same machine. However, there is a mean delay of about 10 msec and a random error of ±7.5 msec (±5 msec on the AT or PS/2). Our analyses show that for typical single response experimental situations, this added variance is acceptable. With mouse buttons, timing resulted in a delay of 31 ±2 msec if the mouse ball was steady but 45 ±15 msec if it was moving, and a 25-msec refractory period before a second response could be detected. With keys connected to the game port, timing was accurate to 1 msec. For timing the interval between two nearly simultaneous responses, only the game port method is recommended. Any research application should provide an external check on reaction timing accuracy and should correct any mean error.     

Time-shrinking: a discontinuity in the perception of auditory temporal patterns.

Recent research at our laboratories in the field of human auditory time perception revealed that the duration of short empty time intervals (less than approximately 200 msec) is considerably underestimated if they are immediately preceded by shorter time intervals. Within a certain range, the amount of subjective time shrinking is a monotonous function of the preceding time interval; the shorter it is, the more it shrinks its successor. In the present study, the preceding interval was kept constant at 50 msec, and the following interval, for which the duration had to be judged, varied from 40 to 280 msec. The results showed that at up to 100 msec, the perceived duration increased to a much lesser extent than did the objective duration. Beyond 120 msec, the perceived duration quickly increased and reached a veridical value at 160 msec. Such a sudden change of perceived duration in a temporal pattern in which the objective duration varies gradually indicates a typical example of categorical perception. We suggest that such a categorization of the time dimension might be a clue for processes of speech and music perception.     

Time-shrinking: A discontinuity in the perception of auditory temporal patterns

Recent research at our laboratories in the field of human auditory time perception revealed that the duration of short empty time intervals (<～200 msec) is considerably underestimated if they are immediately preceded by shorter time intervals. Within a certain range, the amount of subjective time shrinking is a monotonous function of the preceding time interval: the shorter it is, the more it shrinks its successor. In the present study, the preceding interval was kept constant at 50 msec, and the following interval for which the duration had to be judged, varied from 40 to 280 msec. The results showed that at up to 100 msec, the perceived duration increased to a much lesser extent than did the objective duration. Beyond 120 msec, the perceived duration quickly increased and reached a veridical value at 160 msec. Such a sudden change of perceived duration in a temporal pattern in which the objective duration varies gradually indicates a typical example of categorical perception. We suggest that such a categorization of the time dimension might be a clue for processes of speech and music perception.     

PET Flasher: A machine language subroutine for timing visual displays and response latencies

PET Flasher presents a one-line stimulus display at any location on a PET/CBM (Commodore Business Machines) screen and measures reaction time from display onset. Display duration is accurately controlled in 16.7-msec steps, and reaction time measurement is accurate within ±1 msec. PET Flasher is easily incorporated within any PET/CBM BASIC program, since as a subroutine, it is called only when precise timing operations are required.     

Timing accuracy of PC programs running under DOS and Windows

The time in which to press a key and the video retrace interval were measured under various conditions of MS-DOS, Windows 3.1, Windows 3.11, Windows 95, and Windows NT 4.0 Workstation. All the measurements were obtained with the same program running on a single Pentium 300 computer. In all, samples of 1,000 timing measurements were obtained in each of 96 different conditions. Standard deviations of the times ranged from about 0.0006 msec under DOS 6.22 to almost 40 msec under Windows 3.11, representing an increase in timing error of up to 6,000,000%. Researchers requiring millisecond timing accuracy are recommended to use DOS only.     

Studies in auditory timing: 1. Simple patterns

Listeners' accuracy in discriminating one temporal pattern from another was measured in three psychophysical experiments. When the standard pattern consisted of equally timed (isochronic) brief tones, whose interonset intervals (IOIs) were 50, 100, or 200 msec, the accuracy in detecting an asynchrony or deviation of one tone in the sequence was about as would be predicted from older research on the discrimination of single time intervals (6%-8% at an IOI of 200 msec, 11%-12% at an IOI of 100 msec, and almost 20% at an IOI of 50 msec). In a series of 6 or 10 tones, this accuracy was independent of position of delay for IOIs of 100 and 200 msec. At 50 msec, however, accuracy depended on position, being worst in initial positions and best in final positions. When one tone in a series of six has a frequency different from the others, there is some evidence (at IOI = 200 msec) that interval discrimination is relatively poorer for the tone with the different frequency. Similarly, even if all tones have the same frequency but one interval in the series is made twice as long as the others, temporal discrimination is poorer for the tones bordering the longer interval, although this result is dependent on tempo or IOI. Results with these temporally more complex patterns may be interpreted in part by applying the relative Weber ratio to the intervals before and after the delayed tone. Alternatively, these experiments may show the influence of accent on the temporal discrimination of individual tones.     

Duration estimates of two information processing components

Adult humans attempted to make quick responses to the first of two sequentially presented visual stimuli. At short interstimulus intervals (less than about 100 msec) accuracy was impaired by a different second stimulus and this was hypothesized to reflect the activity of an information processing component concerned with stimulus registration. At longer interstimulus intervals (up to approximately 350 msec) reaction time was inhibited by a different second stimulus and this was assumed to reflect the activity of a second component concerned with decision. The stimulus registration component was insensitive to variations in the complexity of the task, while the decision component was found to be greater for a task requiring recognition (is the current stimulus the same as an earlier one?) than for one merely requiring choice (what is the current stimulus?). This functional independence and the sizeable difference in the temporal range of susceptibility led to the conclusion that two distinct information processing components were involved.     

Judging the relative duration of multimodal short empty time intervals

Three experiments address the cause of the different performance levels found in time discrimination of empty intervals with durations near 250 msec. Performance differed according to the kind of sensory modality that marked the intervals. With a procedure in which the type of marker was randomized from trial to trial, it was shown that variability of discrimination judgments could not be attributed entirely to the variability of the criterion on which a judgment was based. Such a randomization slightly affects discrimination but provokes a reorganization related to marker conditions of the probabilities of judging an interval to be short or long. Moreover, it was shown that within intramodal conditions, physical characteristics of markers influence the discrimination performances. To account for the results generated with different marker-type intervals at 250 msec, we propose that two types of processor may be involved in duration discrimination: one is specifically related to a given sensory modality, whereas the other is aspecific and responsible for discrimination of intermodal intervals.     

SCORIT: A computer subroutine for scoring electrodermal responses

Given digitized electrodermal response records sampled at a rate of 20/sec and at a sensitivity level between 140 and 170 ohms, a computer subroutine for scoring skin resistance responses is described. It is designed to score multiple responses on a trial, which makes it particularly suitable for classical conditioning experiments involving long interstimulus intervals. The subroutine returns to the main program response latency, base resistance, peak resistance, and time from base to peak. Since SCORIT is written in FORTRAN IV, it can be employed in virtually any modern central computing facility at costs substantially below those involved in hand scoring.     

Timing accuracy under Microsoft Windows revealed through external chronometry

Recent studies by Myors (1998, 1999) have concluded that the Microsoft Windows operating system is unable to support sufficient timing precision and resolution for use in psychological research. In the present study, we reexamined the timing accuracy of Windows 95/98, using (1) external chronometry, (2) methods to maximize the system priority of timing software, and (3) timing functions with a theoretical resolution of 1 msec or better. The suitability of various peripheral response devices and the relative timing accuracy of computers with microprocessors with different speeds were also explored. The results indicate that if software is properly controlled, submillisecond timing resolution is achievable under Windows with both old and new computers alike. Of the computer input devices tested, the standard parallel port was revealed as the most precise, and the serial mouse also exhibited sufficient timing precision for use in single-interval reaction time experiments.     

The time course of spatial memory distortions

Four experiments investigated the memory distortions for the location of a dot in relation to two horizontally aligned landmarks. In Experiment 1, participants reproduced from memory a dot location with respect to the two landmarks. Their performance showed a systematic pattern of distortion that was consistent across individual participants. The three subsequent experiments investigated the time course of spatial memory distortions. Using a visual discrimination task, we were able to map the emergence of spatial distortions within the first 800 msec of the retention interval. After retention intervals as brief as 50 msec, a distortion was already present. In all but one experiment, the distortion increased with longer retention intervals. This early onset of spatial memory distortions might reflect the almost immediate decay of detailed spatial information and the early influence of an enduring spatial memory representation, which encodes spatial information in terms of the perceived structure of space.