Some notes on conditioned suppression and reinforcement schedules

Two pigeons were trained on an FR 150 schedule of reinforcement. An Estes-Skinner conditioned suppression procedure was then superimposed on this performance at varied intervals. If the CS occurred during the early stages of the ratio run, complete suppression resulted. If the CS occurred during the later stages of the run, the birds continued to respond until the reinforcement was obtained, which was then followed by complete suppression.     

Some effects of relative reinforcement rate and changeover delay in response-independent concurrent schedules of reinforcement

Reinforcements were arranged independently of the pigeon's behavior by concurrent variable-interval schedules. The reinforcements arranged by one of the schedules occurred when the chamber was illuminated with amber light, and the reinforcements arranged by the other schedule occurred when the chamber was illuminated with blue light. Both schedules functioned concurrently, but reinforcers were delivered by each only in the presence of the appropriate stimulus condition. A response on a white key, the only key in the chamber, alternated the stimulus condition and the effective schedule. The results of this procedure were similar to those obtained with concurrent response-dependent variable-interval schedules of reinforcement. The proportion of the total session time spent in the presence of a schedule component approximated the proportion of the total number of reinforcements in the component. Changeover rate was a decreasing function of the changeover delay and of the difference between the relative rates of reinforcement for each pair of concurrent schedules.     

Group behavior of rats under schedules of reinforcement

Groups of three rats were placed in a chamber containing one response lever and one water dispenser. A variety of schedule conditions were explored including fixed ratio, extinction, satiation, fixed interval, fixed time, differential reinforcement of low rates, and discrimination learning. Each group was treated as a single unit, with the collective lever responses emitted by the three rats being the main dependent variable. Group responding was found to be controlled by the reinforcement schedules in an orderly and consistent manner. However, the groups often paused less and responded faster than individual rats working under identical conditions.     

Properties of behavior under random interval reinforcement schedules

In a temporally defined system of reinforcement schedules, the fixed interval case is defined when reinforcement probability, P, is equal to unity for the first response in any cycle length, T; when P is less than 1.0, random interval schedules emerge wherein T/P specifies the expected interval between reinforcements. Key-pecking rates were found to be: (a) inversely related to T/P; (b) higher at T=1.0 second than at other T parameter values; (c) low and linear at several T and T/P values. The mean post-reinforcement pause, if initially small, increased, and if initially large, decreased, as T/P increased.     

Contrast effects in multiple fixed-interval reinforcement schedules

Pigeons were exposed to a multiple fixed-interval one-minute fixed-interval three-minute schedule of reinforcement following training on either a multiple fixed-interval one-minute fixed-interval one-minute schedule or a multiple fixed-interval three-minute fixed-interval three-minute schedule. For all birds, large negative local contrast effects developed during the first of four three-minute intervals in a component; response rate was depressed and postreinforcement pause lengthened in this interval. Positive local contrast effects were evident during the first of 12 one-minute intervals in a component for five of six birds; at asymptote, the pause was very short and response rate slightly elevated during this interval. Overall positive contrast was generally transient and varied considerably across subjects, while overall negative contrast effects, if they occurred, appeared only after a large number of sessions.     

Concurrent reinforcement schedules: behavior change and maintenance without extinction

We evaluated the effects of concurrent schedules of reinforcement on negatively reinforced problem behavior and task completion with 3 children with autism. Results indicated that problem behavior occurred at high levels and relatively few tasks were completed when problem behavior produced a break (from tasks) and task completion produced either no consequence or a break. By contrast, problem behavior was eliminated and tasks were completed when problem behavior produced a break and task completion produced a break with access to preferred activities. Treatment gains were maintained without the use of extinction when the response requirement was increased and the schedule of reinforcement was thinned.     

Effects of reinforcement schedules on rats' choice behavior in extinction.

The effects of reinforcement schedules on rats' choice behavior in extinction were studied. In a free-operant chamber equipped with two retractable bars, the experimental animals were trained to press the bars separately for a food reward. One bar delivered the reward on a continuous reinforcement (CRF) schedule, and the other delivered the reward on a partial reinforcement (PRF) schedule. Control animals earned the reward from both bars with the same reinforcement schedule, either a CRF or a PRF. When both bars were simultaneously available during extinction, the experimental animals responded more frequently to the CRF than to the PRF alternative, demonstrating a reversed within-subjects partial reinforcement extinction effect (PREE). A conventional between-subjects PREE was replicated in the control subjects. The results of this study were inconsistent with both Amsel's (1962, 1967) frustration hypothesis and Capaldi's (1966, 1967) sequential hypotheses.     

Inhibiting function of reinforcement: magnitude effects on variable-interval schedules

In two experiments, the performance of rats under constant-probability and arithmetic variable-interval schedules respectively was compared when the concentration of a liquid reinforcer was varied within sessions; in other sessions, half of the reinforcers were randomly omitted. When the discriminative function of the reinforcer as a signal for a decrease in the probability of reinforcement was attenuated (the constant-probability schedule) the postreinforcement pause duration was nevertheless an increasing function of reinforcer magnitude. This relationship was also present, but more marked, when the temporal discriminative function of the reinforcer was enhanced (the arithmetic schedule). These results suggested that reinforcement has an unconditioned suppressive effect on the reinforced response distinct from any discriminative function it may acquire. The reinforcement-omission effect, where response rate accelerates following omission, was observed when the reinforcer functioned as an effective temporal discriminative stimulus, but not when such temporal control was absent.     

Some factors controlling preference between fixed-ratio and variable-ratio schedules of reinforcement

A multiple schedule of food reinforcement for key-pecking was arranged which consisted of nine fixed-ratios, each of which operated in the presence of a different stimulus. Pigeons could complete a given fixed-ratio within the multiple schedule or, by pecking a second key, could switch from the fixed-ratio schedule to a variable-ratio schedule consisting of the same nine ratios. Stable switching behavior was established which did not maximize simple probability or rate of reinforcement. Instead, the subjects showed a stable preference for the variable-ratio schedule of food reinforcement. Increasing the number of responses required to switch, and removing the occasions on which reinforcement was delivered after a single response in the variable schedule, decreased the number of switches to the variable schedule. Periods of delay interposed between a completed switch and the availability of reinforcement after one response in the variable schedule also decreased switching to the variable schedule, particularly at long delay intervals.     

Changeover behavior under pairs of fixed-ratio and variable-ratio schedules of reinforcement

Three pigeons were studied under a pair of equal fixed-ratio schedules and a pair of equal variable-ratio schedules. Each pair was arranged as independent, concurrent schedules and also in a non-independent relation where each peck in a schedule counted toward the response requirement of both schedules. The non-independent pair of variable-ratio schedules maintained much higher changeover rates than any of the other three arrangements. Thus, two factors seemed necessary for generating high changeover rates. Responding on a schedule had to count toward the response requirement of both schedules, and the component schedules had to be variable. These data are consistent with the hypothesis that changeovers are at least partly controlled by the probability of reinforcement following a changeover.     

Spatiotemporal patterns of behavior produced by variable-interval schedules of reinforcement

The spatiotemporal patterns of behavior exhibited by two pigeons during a variable-interval 15-second schedule of food reinforcement, a variable-interval 5-minute schedule, and then extinction of key pecking were recorded using an apparatus that continuously tracked the position of the bird in the experimental chamber. The variable-interval 15-second schedule produced a close-to-key pattern between reinforcements with two types of regular excursions from the region of the key frequently occurring after reinforcement. Subsequent exposure to the variable-interval 5-minute schedule produced more extended and extremely regular patterns between responses. Reinstatement of the variable-interval 15-second schedule reestablished the close-to-key pattern with regular excursions frequently occurring after reinforcement. During extinction the spatiotemporal patterns that had developed during the variable-interval 5-minute schedule reappeared and gradually dissipated. These patterns may have been a form of superstitious behavior.     

Some effects on generalization gradients of tandem schedules

The relationship between training conditions and stimulus generalization gradients was examined using tandem schedules of reinforcement. Schedules were selected so that frequency of reinforcement and rate of responding were varied somewhat independently of each other. A peak-shift in the generalization gradient was obtained when extinction had been associated with one of the stimuli. No comparable peak shift was obtained when there were equal response rates in the training stimuli even with dissimilar frequencies of reinforcement. The data imply that response rates at the end of training, rather than reinforcement frequency per se, determine the characteristics of the generalization gradient.     

Second-order schedules of token reinforcement with pigeons: effects of fixed- and variable-ratio exchange schedules

Pigeons' key pecks produced food under second-order schedules of token reinforcement, with light-emitting diodes serving as token reinforcers. In Experiment 1, tokens were earned according to a fixed-ratio 50 schedule and were exchanged for food according to either fixed-ratio or variable-ratio exchange schedules, with schedule type varied across conditions. In Experiment 2, schedule type was varied within sessions using a multiple schedule. In one component, tokens were earned according to a fixed-ratio 50 schedule and exchanged according to a variable-ratio schedule. In the other component, tokens were earned according to a variable-ratio 50 schedule and exchanged according to a fixed-ratio schedule. In both experiments, the number of responses per exchange was varied parametrically across conditions, ranging from 50 to 400 responses. Response rates decreased systematically with increases in the fixed-ratio exchange schedules, but were much less affected by changes in the variable-ratio exchange schedules. Response rates were consistently higher under variable-ratio exchange schedules than tinder comparable fixed-ratio exchange schedules, especially at higher exchange ratios. These response-rate differences were due both to greater pre-ratio pausing and to lower local rates tinder the fixed-ratio exchange schedules. Local response rates increased with proximity to food under the higher fixed-ratio exchange schedules, indicative of discriminative control by the tokens.     

Short-component multiple schedules: effects of relative reinforcement duration

Pigeons were exposed to multiple variable-interval 2-min variable-interval 2-min schedules of food presentation in which relative duration of food presentation was manipulated. When components alternated every 5 sec and were scheduled on separate response keys, relative response rates closely matched relative reinforcement duration in three of four pigeons. On the other hand, relative response rates were insensitive to relative reinforcement duration when components scheduled on a single response key alternated every 5 sec, and when components scheduled on separate response keys alternated every 2 min. Thus, both rapid alternation and spatial separation of components were necessary to produce approximate matching of relative responding to relative reinforcement duration. This finding contrasts with previous findings that only rapid component alternation is necessary for matching when relative rate of reinforcement is manipulated.     

Signalled reinforcement and multiple schedules

The responses of four pigeons were first reinforced in the presence of two different wave-lengths (green and red) on a two-ply multiple schedule with identical variable-interval 3-min schedules of reinforcement associated with each component. While the constant-component reinforcement schedule remained unchanged during the experiment, the schedule associated with the variable component was changed to (1) signalled variable time, (2) unsignalled variable time, or (3) signalled variable interval. The probability with which the availability of the reinforcer was signalled in the variable-interval schedules was either 0.5 or 1.0. Positive contrast occurred in both signalled variable-interval and variable-time schedules, but only when the availability of all the variable-component reinforcers was signalled. Signalling the availability of only 50% of the reinforcers in signalled variable-interval schedules resulted in negative induction. The present data suggest that positive behavioral contrast resulting from signalled reinforcer availability is due to the presence of an extinction-correlated stimulus.