Delayed reinforcement in a multiple schedule

Three rats and a pigeon were first trained on a two-component multiple schedule in which reinforcement in the two components occurred immediately after a response. Later, reinforcement in one component was delayed by a few seconds. During both stages of the experiment, reinforcement was scheduled by equal variable- (pigeon) or random-interval (rats) schedules in the two components. The main effect of the delayed reinforcement was to increase the rate of responding in the unchanged (non-delay) component. This behavioral contrast effect did not appear in all cases to be dependent upon a reduction in the rate of responding or the frequency of reinforcement in the delay component. This finding suggests that a reduction in response rate and/or reinforcement frequency in one component of a multiple schedule may not be a necessary prerequisite for the occurrence of behavioral contrast. This finding is, however, consistent with an explanation that suggests that behavioral contrast results from the introduction of a less-preferred condition in one component of a multiple schedule, since it is known that animals “prefer” immediate to delayed reinforcement.     

A comparison of two models for performance under fixed interval schedules of reinforcement

Two models are proposed for responding under fixed-interval schedules of reinforcement. The first model is a Poisson model and seems suitable for situations in which responding produces a classical “FI scallop”. A second model is then developed to describe “break and run” performance, which is also known to occur under some Fixed Interval schedules. The models do not however give any indication of the circumstances under which a particular mode of responding should arise. A comparison of the models to a small set of data collected from rats performing under an FI 60 sec schedule indicates that for the data considered, the second model (a State model) produced by far the best fit.     

Effects of pre-operant running and sucrose concentration on operant wheel running on a fixed interval schedule of reinforcement

Prior research proposed that temporal control over the pattern of operant wheel running on a fixed interval (FI) schedule of sucrose reinforcement is a function of automatic reinforcement generated by wheel running and the experimentally arranged sucrose reinforcement. Two experiments were conducted to assess this prediction. In the first experiment, rats ran for different durations (0, 30, 60, and 180 min) prior to a session of operant wheel running on a FI 120-s schedule. In the second experiment, the concentration of sucrose reinforcement on a FI 180-s schedule was varied across values of 0, 5, 15, and 25%. In Experiment 1, as the duration of pre-operant running increased, the postreinforcement pause before initiation of running lengthened while wheel revolutions in the latter part of the FI interval increased. In Experiment 2, wheel revolutions markedly increased then decreased to a plateau early in the FI interval. Neither manipulation increased temporal control of the pattern of wheel running. Instead, results indicate that operant wheel running is regulated by automatic reinforcement generated by wheel activity and an adjunctive pattern of running induced by the temporal presentation of sucrose. Furthermore, the findings question whether the sucrose contingency regulates wheel running as a reinforcing consequence.     

Delayed reinforcement and runway performance

The Psychological Record -     

Random interval schedules of reinforcement

A method for generating a reinforcement schedule that closely approximates idealized VI schedules in which reinforcement assignments occur randomly in time (RI schedules) is described. Response rates of pigeons exposed for 20 sessions to this schedule appeared very similar to response rates characteristic of arithmetic series VIs. The distribution function describing these schedules was derived and its relations to other VI distributions, as well as to FI and random ratio (RR) were shown.     

A fixed interval schedule in which the interval is initiated by a response

The fixed interval schedule described requires the animal to initiate every time interval by making a response on a bar other than the one on which it is reinforced. This response, R_A, demarcates the postreinforcement pause (S^R-R_A interval) from the fixed interval pause (R_A-R_B interval) so that these pauses may be measured separately. Twelve rats and three monkeys, working in two-bar Skinner boxes, were trained and stabilized on this schedule. The resulting performances, presented for individual animals, are analyzed in terms of (1) the relative frequencies with which the animal waits various lengths of time between consecutive responses, (2) the relative frequencies with which various rates of responding appear, (3) the change in response rate throughout the fixed interval, (4) the average length of the postreinforcement pause, (5) the relative frequencies with which the animal waits different lengths of time between the R_A and the first R_B, and (6) the average inter-response time as a function of the rank order in the fixed interval of the inter-response time. The joint interpretation of the several measures taken leads to the following conclusions: 1. The probability of an R_B increases throughout the fixed interval. 2. The increase is discontinuous at the first R_B, at which point the probability increases sharply. 3. The frequency distributions of R_A-R_B pauses exhibit three discrete types of behavior with no intermediate cases. 4. The (main) mode of R_A-R_B interval length usually occurs just below the fixed interval requirement.     

Schedule-induced polydipsia as a function of fixed interval length

Rats were trained to bar-press for Noyes pellets on an FI schedule which was increased serially through several values from 2 sec to as high as 300 sec. Concurrently, water was freely available. As FI length was increased, the degree of polydipsia increased linearly to a maximum value.     

Delayed reinforcement of fixed-ratio performance without mediating exteroceptive conditioned reinforcement

The performance of pigeons was studied under conditions in which the completion of a fixed-ratio requirement was not contiguous with the presentation of a reinforcer. Timein and timeout periods alternated throughout the experimental sessions. Responses made by an experimental bird during the timein period were accumulated, and when a fixed-ratio requirement had been met, grain was presented to the experimental bird and a yoked control following their first response in the next timein period. Across most manipulations of the fixed-ratio requirement and of the duration of the timeout period, the response rates of the experimental birds were considerably higher than those of their controls, suggesting that the response-reinforcer dependency controlled the behavior of the experimental bird in the absence of a close temporal association between responding on the ratio schedule and reinforcer presentations.     

Varying reinforcement magnitude on interval schedules

In Experiment 1, rats were trained on either a random-interval or a variable-interval 60-sec schedule of reinforcement, and reinforcement magnitude was varied across conditions between one and four pellets. Although the two schedules maintained different patterns of behaviour, patterns and rates of responding were not systematically affected by the variation in reinforcement magnitude. In Experiment 2, a regulated probability interval schedule that generated similar rates of reinforcement to those of the schedules of Experiment 1 was used, with the pattern of behaviour generated resembling that typical of a random-interval schedule. Changing reinforcement magnitude again produced few systematic changes in behaviour. In Experiment 3, a variable-ratio schedule was used within a procedure that otherwise resembled that of Experiments 1 and 2. Increasing the reinforcement magnitude now decreased the rates of responding, and examination of the patterns of responding showed that this came about because rates of responding were higher early in the interreinforcer interval in the one-pellet condition. These experiments demonstrate the insensitivity of behaviour under interval schedules to changes in reinforcement magnitude and suggest the operation of mechanisms different from those engaged by ratio schedules and discretetrial learning procedures.     

Fixed interval schedules and delay of reinforcement

In a fixed interval schedule of reinforcement the only responses to be reinforced are those made when a certain time interval has elapsed since the previous reinforcement. The behaviour of three rats on such a schedule was compared with their behaviour on a schedule where a response made at any time during the interval was reinforced by setting up a reward which was delivered when the interval had elapsed. Response rates were higher in the ordinary fixed interval schedule than in its modified version, and it is argued that this rules out attempts to explain the maintenance of fixed interval performance by delayed reinforcement. Despite the clear difference in response rates, there was considerable similarity between the post-reinforcement pauses developed in the two schedules, and this suggests that pausing is influenced more by temporal than by response contingencies.     

Delayed reinforcement,selective learning and habit reversal

The Psychological Record - Three groups of hungry rats were trained in a T maze position response under conditions of 20-sec. delay of food reinforcement on 0, 50, and 100 per cent of the correct...     

Delayed effects of practiced versus unpracticed responses after observation of movie violence

University men participating in an ostensible study of “impression formation” first received either an insulting or neutral evaluation of themselves from their supposed partner and then watched either a prize fight or an exciting but nonaggressive scene. After this, they either had an opportunity to evaluate their partner right away or they had to wait an hour before evaluating him. On scoring the subjects' written statements about the partner (to be seen by him and the experimenter), it was found that (1) for those given the immediate opportunity to be aggressive, the violent movie increased the strength of the angered subjects' initial attack on their partner over that displayed by the similarly insulted men shown the nonaggressive film; (2) if the angry subjects had to wait an hour before evaluating their partner, there was no difference between the aggressive and nonaggressive movie groups; (3) the aggression-heightening effect of the violent scene did carry over the intervening hour, however, if the insulted men had been given the earlier opportunity to evaluate their partner. It is suggested that the performance of an aggressive response soon after seeing an aggressive film increases the persistence of the aggressive reactions over time.