Biomedical subjects

H A Broadbent

Publications and source records attributed to H A Broadbent.

5 recordsLinked to original sources

PubMed1997

Systematic nonlinearities in the memory representation of time.

The representation of time was investigated by testing rats with intervals that changed by 2 s across trials. In Experiment 1, 2 ranges (20-150 s, 30-160 s; n = 10 rats per group) were examined. The times at which response bursts occurred (start time) were approximately proportional to interval durations. However, systematic departures from linearity were observed. Nonlinearities were related to the absolute duration of intervals, rather than to durations relative to the range. In Experiment 2, 660-s trials were inserted into the sequence of intervals (10-140 s, n = 20). Start and end times of response bursts were approximately proportional to intervals, but nonlinearities in start and end times were correlated, indicating that the source of nonlinearity was in the memory representation of time rather than in a decision process. These results indicate that the representation of time is nonlinearly related to physical time.

Animals↗

PubMed1994

Preferred rates of repetitive tapping and categorical time production.

In a constrained finger-tapping task, in which a subject attempts to match the rate of tapping responses to the rate of a pacer stimulus, interresponse interval (IRI) was a nonlinear function of interstimulus interval (ISI), in agreement with the results of Collyer, Broadbent, and Church (1992). In an unconstrained task, the subjects were not given an ISI to match, but were instructed to tap at their preferred rate, one that seemed not too fast or too slow for comfortable production. The distribution of preferred IRIs was bimodal rather than unimodal, with modes at 272 and 450 msec. Preferred IRIs also tended to become shorter over successive sessions. Time intervals that were preferred in the unconstrained task tended to be intervals that were overproduced (IRI > ISI) when they were used as ISIs in the constrained task. A multiple-oscillator model of timing developed by Church and Broadbent (1990) was used to simulate the two tasks. The nonlinearity in constrained tapping, termed the oscillator signature, and the bimodal distribution in unconstrained tapping were both exhibited by the model. The nature of the experimental results and the success of the simulation in capturing them both provide further support for a multiple-oscillator view of timing.

Female↗

PubMed1994

Periodic behavior in a random environment.

Animals' tendency to search periodically in temporally random environments was studied by presenting rats with random-interval (RI) 60-s and 120-s schedules. Power spectra revealed a periodicity of responding of 20-50 s for all animals regardless of condition. A second periodicity of 5-10-s was strongest under the RI 60-s schedule. Optimality theory suggests that periodic responding is better than random responding in obtaining food sooner on average, but the theory does not account for multiple periodicities. These multiple periodicities also cannot be explained by a single-oscillator, information-processing version of scalar expectancy theory (J. Gibbon & R. M. Church, 1992) or by the behavioral theory of timing (P.R. Killeen & J. G. Fetterman, 1988). The periodicities are consistent with a connectionist version of scalar expectancy theory that has nonscalar emergent properties, including multiple periodicities that are not proportional to the rate of random events.

Animals↗

PubMed1992

Categorical time production: evidence for discrete timing in motor control.

Subjects performed a repetitive manual tapping task, attempting to match a given rate of auditory stimulus pulses, first with the pulses audible (synchronization) and then with the pulses turned off (continuation). In different sessions, the interstimulus interval (ISI) was selected from the range 175 to 825 msec in steps of 25 msec, with different ISI values presented in a random order. Across this range of ISI conditions, interresponse intervals (IRIs) exhibited alternating positive bias (too slow) and negative bias (too fast). We interpret this pattern of bias in terms of a discrete, or categorical, timing mechanism in motor timing. Categorical time production can be viewed as extending our conception of the timekeeper in Wing's (Wing & Kristofferson, 1973a, 1973b) two-process model of motor timing and may be related to the system of multiple clocks proposed by Kristofferson (1980) to explain a categorical pattern of variability measures in duration discrimination.

Adult↗

PubMed1990

Alternative representations of time, number, and rate.

Three facts of time perception are described based upon a temporal generalization task for rats (the peak procedure) in which food reinforcement is delivered on half the trials following the first lever-press response after some fixed interval after signal onset. (1) The mean response rate as a function of time is a smooth, slightly asymmetric, function with a maximum near the time of reinforcement; (2) the response rate on individual trials is characterized by an abrupt change from a state of low responding to a state of high responding and finally another state of low responding (break-run-break pattern); and (3) the mean response rate in 12-s and 20-s peak procedures is similar when plotted against time relative to the time of reinforcement (superposition). An information-processing version of scalar timing theory is described and compared to an alternative connectionist version of scalar timing theory that involves multiple oscillators and an autoassociation network. Psychological, mathematical and biological descriptions of the two versions are described and some possible extensions of the connectionist version are proposed to deal with perception of number, rate, and spatial orientation.

Animals↗