Studies of operant and reflexive key pecks in the pigeon

The duration of pigeons' key pecks was studied in three experiments. Experiment I revealed that key pecks early in exposure to continuous reinforcement were of short duration, as were key pecks observed on an omission procedure in which pecks prevented food delivery. Key pecks later in exposure to continuous reinforcement, and those that occurred on positive automaintenance procedures, were of long duration. In Experiment II, pigeons were exposed to fixed-interval and fixed-ratio reinforcement schedules, and durations were recorded separately for each quarter of each interval or ratio. On fixed interval, durations were shorter in the first quarter of each interval than in subsequent quarters; on fixed ratio, durations were longer in the first quarter of the ratio than in subsequent quarters. These data parallel observations of concurrent operant responding and salivation in dogs. In Experiment III, pigeons were exposed to a discrete trial, differential-reinforcement-of-low-rate 6-sec schedule. Durations of responses in the first 2 sec of the trial were substantially shorter than those of responses that occurred later. The data from all three experiments support the view that the pigeon's "key peck" actually consists of two subclasses of peck, one reflexive and one operant.     

Evaluating interobserver reliability of interval data

Previous recommendations to employ occurrence, nonoccurrence, and overall estimates of interobserver reliability for interval data are reviewed. A rationale for comparing obtained reliability to reliability that would result from a random-chance model is explained. Formulae and graphic functions are presented to allow for the determination of chance agreement for each of the three indices, given any obtained per cent of intervals in which a response is recorded to occur. All indices are interpretable throughout the range of possible obtained values for the per cent of intervals in which a response is recorded. The level of chance agreement simply changes with changing values. Statistical procedures that could be used to determine whether obtained reliability is significantly superior to chance reliability are reviewed. These procedures are rejected because they yield significance levels that are partly a function of sample sizes and because there are no general rules to govern acceptable significance levels depending on the sizes of samples employed.     

Discriminative properties of briefly presented stimuli

In Experiment I, pigeons' responses produced food according to a fixed-interval schedule while responses on the key also produced brief stimuli according to a variable-interval schedule. Each brief stimulus reset the fixed interval. Thus, a brief stimulus occurred irregularly but a fixed minimum time separated the occurrence of food from a brief stimulus. Pauses followed brief stimuli and were followed by an accelerated response rate until another brief stimulus or food occurred. In Experiment II, four control procedures were examined. (1) Brief-stimulus presentations were omitted, producing a loss of response patterning. (2) A second-order schedule was studied with fixed-interval components. This schedule produced patterning following brief stimuli similar in kind and degree to that found in Experiment I. (3) A conjoint schedule was arranged in which food was no longer separated from the stimulus by a fixed time; pauses following the stimulus no longer resulted. (4) A brief food reinforcer replaced the brief visual stimulus, resulting in a constant response rate with no pausing following the brief food stimulus. The results suggest that the brief-stimulus effects were due to discriminative functions produced by the fixed temporal relation separating the stimulus from food.     

Trace autoshaping: Acquisition, maintenance, and path dependence at long trace intervals

The pigeon's tendency to acquire and maintain signal-directed key pecking under a trace conditioning procedure was parametrically examined. In Experiment 1, the percentage of CS trials with a key peck response was a decreasing function of the trace interval for separate groups of pigeons. The majority of subjects acquired signal-directed key pecking with trace intervals as long as 36 sec. In Experiment 2, differential maintenance of key pecking occurred across trace intervals in a within-subject procedure. Maintenance of key pecking at 36- and 60-sec trace intervals was path dependent in that responding depended on the subject's performance under the preceding trace interval.     

Delayed choice responding by pigeons when the correct response is not predictable from the sample stimulus.

Food-deprived pigeons were presented with a row of four response keys situated above a grain hopper aperture. At the start of a trial, three of four keys were randomly selected and illuminated white for six seconds. After a variable blackout period, one of the three previously white keys and the previously dark key were illuminated green, and the remaining white keys were reilluminated as before. A response to the green key that was previously white was reinforced with three-second access to gain, a response to any other key resulted in a three-second blackout and the start of a new trial. Five of six subjects responded to the correct green key more often than chance at an interstimulus interval of 1.5 seconds, and they displayed maximal performance at different intertrial interval values ranging from 15 to 60 seconds. Choice accuracy decreased for all but one subject as the interstimulus interval was increased. For the range of interstimulus interval durations employed, decrements in choice accuracy were qualitatively similar to, but lower than those typically obtained from, delayed-matching-to-sample or delayed-pair comparison procedures.     

Schedule-induced defecation.

Excessive defecation, typically considered to be a concomitant of stress, was experimentally induced or eliminated under specific schedules of positive reinforcement of lever pressing by rats. The schedules were, by and large, those under which polydipsia is typically induced. In the first of three experiments, rats under fixed-interval 32-second schedules and variable interval 32-second schedules for food and water reinforcers defecated profusely, but not under fixed-interval one-second schedules or other small interval schedules. Somewhat higher rates of defecation were observed on variable interval 32-second schedules than on fixed-interval 32-second schedules. In a second experiment, fixed-ratio schedules were used, some of which resulted in responding such that reinforcement densities were similar to those on the interval schedules that induced defecation. Defecation was not systematically induced by these ratio schedules. In a third experiment, fixed-time schedules of food presentations were utilized. High rates of defecation were induced comparable to those induced by interval schedules of the same time parameter. No other behavior commonly termed "emotional" was observed in any of these experiments.     

Concurrent choice: Effects of overall reinforcer rate and the temporal distribution of reinforcers

Six pigeons responded on a series of concurrent exponential variable-interval schedules, offering a within-subject comparison with previously published data from concurrent arithmetic variable-interval schedules. Both relative and overall reinforcer rates were varied between conditions. The generalized matching law described the data well, with undermatching much more frequent than strict matching. Time-allocation sensitivity consistently exceeded response-allocation sensitivity for both schedule types, and exponential-schedule sensitivity exceeded arithmetic-schedule sensitivity for both measures of choice. A further set of conditions using variable-interval schedules whose shortest interval was correlated with the mean interval, like arithmetic schedules, but that provided a constant conditional probability of reinforcement, like exponential schedules, produced sensitivities between those produced by conventional arithmetic and exponential schedules. Unlike previous arithmetic-schedule results, exponential sensitivity changed nonmonotonically with changes in overall reinforcer rate. The results clarify our knowledge of the effects of arithmetic and exponential schedules but confuse our understanding of the effects of overall reinforcer rate on concurrent choice.     

THE ACCELERATED INTAKE: A METHOD FOR INCREASING INITIAL ATTENDANCE TO OUTPATIENT COCAINE TREATMENT

We examined whether offering an accelerated (same-day) versus a standard (1- to 7-day delay) intake appointment increased initial attendance at an outpatient cocaine treatment program. Significantly more of the subjects who were offered an accelerated intake (59%) attended than those who were given a standard intake (33%), χ² (2, N = 78) = 4.198, p < .05. The accelerated intake procedure appears to be useful for enhancing enrollment in outpatient addiction treatment.     

The behavioral theory of timing: Reinforcer rate determines pacemaker rate

In the behavioral theory of timing, pulses from a hypothetical Poisson pacemaker produce transitions between states that are correlated with adjunctive behavior. The adjunctive behavior serves as a discriminative stimulus for temporal discriminations. The present experiments tested the assumption that the average interpulse time of the pacemaker is proportional to interreinforcer interval. Responses on a left key were reinforced at variable intervals for the first 25 s since the beginning of a 50-s trial, and right-key responses were reinforced at variable intervals during the second 25 s. Psychometric functions relating proportion of right-key responses to time since trial onset, in 5-s intervals across the 50-s trial, were sigmoidal in form. Average interpulse times derived by fitting quantitative predictions from the behavioral theory of timing to obtained psychometric functions decreased when the interreinforcer interval was decreased and increased when the interreinforcer interval was increased, as predicted by the theory. In a second experiment, average interpulse times estimated from trials without reinforcement followed global changes in interreinforcer interval, as predicted by the theory. Changes in temporal discrimination as a function of interreinforcer interval were therefore not influenced by the discrimination of reinforcer occurrence. The present data support the assumption of the behavioral theory of timing that interpulse time is determined by interreinforcer interval.     

Intertrial-interval effects on sensitivity (A') and response bias (B") in a temporal discrimination by rats.

Killeen and Fetterman's (1988) behavioral theory of animal timing predicts that decreases in the rate of reinforcement should produce decreases in the sensitivity (A') of temporal discriminations and a decrease in miss and correct rejection rates (decrease in bias toward "long" responses). Eight rats were trained on a 10- versus 0.1-s temporal discrimination with an intertrial interval of 5 s and were subsequently tested on probe days on the same discrimination with intertrial intervals of 1, 2.5, 5, 10, or 20 s. The rate of reinforcement declined for all animals as intertrial interval increased. Although sensitivity (A') decreased with increasing intertrial interval, all rats showed an increase in bias to make long responses.