Runway acquisition and extinction as a joint function of magnitude of reward and percentage of rewarded acquisition trials

To determine the joint effects of partial reward and reward magnitude on acquisition and extinction rates, and on acquisition and extinction asymptotes, 215 Wistar albino rats were trained in a Hunter straight runway. The experimental design was a 4 × 4 × 2 factorial combining four reward magnitudes, four reward percentages, and two experimenters. The data revealed that the acquisition rate was an increasing function of both percentage and magnitude of reward and that neither reward magnitude nor percentage of reward significantly affected acquisition asymptote. For extinction, it was found that, for continuous schedules, the larger the reward magnitude the less the resistance to extinction and, for partial schedules, the larger the reward magnitude the greater the resistance to extinction. These results were interpreted within the framework of the sequential effects hypothesis (Capaldi, 1966).     

Magnitude of negative reinforcement and resistance to extinction

In the first experiment rats experienced large or small magnitude of negative reinforcement (shock reduction) in a straight alley. Half of the subjects in each magnitude group received continuous reinforcement, and the other half received a 50% partial reinforcement schedule (nonreinforcement consisting of no shock reduction in the goal box). In extinction the groups were ordered: large partial > small-partial > small-continuous > large-continuous. In the second experiment rats received large, small and nonreinforcement in various sequences using the runway-negative reinforcement procedure and were ordered: SNL>LNL>SNL>LNS in resistance to extinction (letters represent the magnitudes in the sequence experienced in acquisition). The results of these experiments indicate a commality between positive and negative reinforcement with respect to behavioral phenomena and theoretical accounts of those phenomena.     

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.     

Order of partial and consistent reward,reward magnitude shift,and resistance to extinction

In a separate-phase runway experiment with rats, four schedules involving partial (P) and consistent (C) reward (CC, CP, PC, and PP) were crossed with three reward magnitude shift conditions (upshift, nonshift, and downshift). The data revealed three major findings: (a) Reward magnitude downshift generally led to rapid extinction; (b) consistent reward prior to partial reward (CP) resulted in slower extinction than the reverse order (PC) under conditions of reward magnitude shift (particularly downshift); and (c) the relative performance of PC and CP under conditions of reward magnitude shift was reversed from postshift to extinction. On the basis of these data it was suggested that processes not presently identified by reinforcement level theory and stimulus analyzer theory influence extinction following separate-phase acquisition. A modification of reward level theory was presented to provide an account of extinction performance following separate-phase reward reduction.     

Schedule-induced drinking as a function of percentage reinforcement

Drinking was recorded in rats while lever pressing was maintained on a series of percentage reinforcement schedules in which the per cent of 1-min fixed intervals terminating with food was 100, 90, 30, 70, 10, 50, and 100%. Intervals in which a pellet was omitted were terminated by brief light flash and click stimuli that were also correlated with food presentations. Drinking failed to develop in five of six subjects following intervals in which the brief stimuli were presented regardless of percentage reinforcement. Postpellet drinking, which followed intervals terminated with pellet delivery, however, increased in both duration and amount ingested per interval as percentage reinforcement was systematically decreased. The increase in postpellet drinking above that produced by 100% reinforcement was interpreted as an analogue of the positive-contrast effect observed with food-reinforced operants.