Resistance to extinction following variable-interval reinforcement: reinforcer rate and amount

Rats obtained food-pellet reinforcers by nose poking a lighted key. Experiment 1 examined resistance to extinction following single-schedule training with different variable-interval schedules, ranging from a mean interval of 16 min to 0.25 min. That is, for each schedule, the rats received 20 consecutive daily baseline sessions and then a session of extinction (i.e., no reinforcers). Resistance to extinction (decline in response rate relative to baseline) was negatively related to the rate of reinforcers obtained during baseline, a relation analogous to the partial-reinforcement-extinction effect. A positive relation between these variables emerged, however, when the unit of extinction was taken as the mean interreinforcer interval that had been in effect during training (i.e., as an omitted reinforcer during extinction). In a second experiment, rats received blocks of training sessions, all with the same variable-interval schedule but with a reinforcer of four pellets for some blocks and one pellet for others. Resistance to extinction was greater following training with the larger (four pellets) than with the smaller (one pellet) reinforcer. Taken together, these results support the principle that greater reinforcement during training (e.g., higher rate or larger amount) engenders greater resistance to extinction even when the different conditions of reinforcement are varied between blocks of sessions.     

Bouts of responding from variable-interval reinforcement of lever pressing by rats

Four rats obtained food pellets by lever pressing. A variable-interval reinforcement schedule assigned reinforcers on average every 2 min during one block of 20 sessions and on average every 8 min during another block. Also, at each variable-interval duration, a block of sessions was conducted with a schedule that imposed a variable-ratio 4 response requirement after each variable interval (i.e., a tandem variable-time variable-ratio 4 schedule). The total rate of lever pressing increased as a function of the rate of reinforcement and as a result of imposing the variable-ratio requirement. Analysis of log survivor plots of interresponse times indicated that lever pressing occurred in bouts that were separated by pauses. Increasing the rate of reinforcement increased total response rate by increasing the rate of initiating bouts and, less reliably, by lengthening bouts. Imposing the variable-ratio component increased response rate mainly by lengthening bouts. This pattern of results is similar to that reported previously with key poking as the response. Also, response rates within bouts were relatively insensitive to either variable.     

Sequential patterns in post-reinforcement pauses on fixed-interval schedules of food

Responding by one pigeon was reinforced with food on fixed-interval schedules of 30, 60, and 300 sec duration. A second pigeon was studied under fixed-interval durations of 60 and 300 sec. For both birds, the average post-reinforcement pause was one-half the duration of the fixed interval. Autocorrelation coefficients revealed first-order sequential dependencies in series of post-reinforcement pauses. On the 300-sec fixed-interval schedule, successive post-reinforcement tended to alternate between long and short durations. At the shorter fixed-interval durations there was less evidence of alternation sequences. A second experiment was conducted to determine if the time intervals between the first response after reinforcement and the next reinforcement (the work periods) were responsible for the alternation patterns in the series of post-reinforcement pauses. To evaluate the role of the work period, several procedures were used to modify the work period from that obtained on the fixed-interval 300-sec schedule. Adding a schedule to the fixed-interval schedule that set the minimum amount of time that could elapse between the first response after reinforcement and the next reinforcement eliminated the alternation pattern. Control schedules indicated that the elimination of alternation patterns resulted from constraints on the work period per se and not from confounded changes in the interreinforcement 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.     

A response-initiated fixed-interval schedule of reinforcement

On a tandem fixed-ratio one fixed-interval schedule, the first response after reinforcement initiates a fixed interval of time and the first response after the interval has elapsed is reinforced. Pigeons trained with that schedule of food reinforcement paused after reinforcement for a period of time that approximated the fixed-interval duration for values of that duration ranging from 3.75 to 60 sec. Cumulative records revealed response patterns best described as break-and-run.