Effects of US-Presentation and CS-termination contingencies on avoidance extinction following partial and continuous reinforcement

The present study assessed the role of both the US-presentation (punishment) and CS-termination contingencies on the maintenance of the shuttlebox avoidance responding in gerbils following acquisition under either partial reinforcement (PR) or continuous reinforcement (AV). Following PR, a stronger relationship obtained between delay of CS termination CR frequency than was found between delay of punishment and extinction performance. Following AV training, however, delay of CS termination and delay of punishment were equally effective determinants of avoidance extinction. These results were interpreted in terms of both the enhanced efficacy of the CS-termination contingency, possibly due to its increased informational value, and the attenuation of punishment suppression in PR-trained Ss.     

Resistance to extinction in the goldfish following schedules of continuous and variable interval reinforcement

Four goldfish (Carassius auratus, comet) were reinforced with food when they intercepted a beam of light. Each fish performed on both CRF and VI 50-sec schedules. In subsequent extinctions, the CRF schedule produced more responses on the first day than did VI, but after the first day the post-CRF rate dropped much more rapidly. These results agree with those previously obtained in birds and mammals.     

Resistance to continuous delay of reinforcement or extinction following partial delay or partial reinforcement in acquisition: A direct comparison

Rats received either partial reward (PR) or partial delay (PD) in acquisition with one, two, or three delay or nonreward trials followed by an immediately rewarded trial or one delay or nonreward trial followed by an immediately rewarded trial. These four groups were then split in half and given either continuous delay or continuous nonreward (extinction) in a “response persistence” phase. In addition, two continuously reinforced groups, one experiencing continuous delay, and the other experiencing extinction were included. The results showed that response persistence was greater when PD groups were given continuous delay rather than extinction, but the opposite was true for PR groups. The “length” (1, 2, or 3 versus 1 nonreward or delay trial) also transferred to the response persistence phase with the length 1, 2, and 3 conditions being more persistent than the 1 length conditions. The results were discussed with respect to theoretical notions of response persistence.     

Early extinction effects following intermittent reinforcement: Little evidence of extinction bursts

The occurrence of extinction bursts—transient increases in response rate in excess of those observed in baseline during the period immediately following discontinuation of reinforcement of a response—was examined. In Experiment 1, key pecking of pigeons was reinforced according to a multiple schedule in which a variable-ratio schedule alternated with an interval schedule in which the reinforcers were yoked to the preceding variable-ratio component. In Experiments 2 and 3, rats were screened such that the lever-press response rates of different rats maintained by variable-interval schedules were either relatively high or relatively low. Following these baseline conditions, in Experiments 1 and 2 responding was extinguished by eliminating the food reinforcer and in Experiment 3 by removing the response–reinforcer dependency. Responses immediately following extinction implementation were examined. Response increases relative to baseline during the first 20 min of a 324.75-min extinction session (Experiment 1) or during the first 30-min extinction session (Experiments 2 and 3) were rare and unsystematic. The results (a) reinforce earlier meta-analyses concluding that extinction bursts may be a less ubiquitous early effect of extinction than has been suggested and (b) invite further experimentation to establish their generality as a function of preceding reinforcement conditions.     

Perseveration of the partial reinforcement effect in extinction with rats over two phases of extinction and two stages of continuous reinforcement

One group of 10 male albino rats was given partial reinforcement while the other 10 rats received continuous reinforcement in a straight alley. Subjects then experienced five consecutive stages of Extinction 1, Continuous Reinforcement 1, Extinction 2, Continuous Reinforcement 2, and finally, Extinction 3. Analysis showed the partial reinforcement effect in extinction was sustained over two stages of extinction and two stages of continuous reinforcement, since subjects receiving partial reinforcement ran faster than rats given continuous reinforcement throughout all three of the extinction periods. The results seem to support those of Amsel's (1967) and Cabpaldi's (1967) theoretical formulations of the partial reinforcement effect in extinction.     

Variability of response location for pigeons responding under continuous reinforcement, intermittent reinforcement, and extinction

The effect of several reinforcement schedules on the variability in topography of a pigeon's key-peck response was determined. The measure of topography was the location of a key peck within a 10-in. wide by 0.75-in. high response key. Food reinforcement was presented from a magazine located below the center of the response key. Variability in response locus decreased to a low value during training in which each response produced reinforcement. Variability increased when fixed intervals, variable intervals, random intervals, or extinction were scheduled.     

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.     

Response cost effects during extinction following fixed-interval reinforcement in humans

This study examined the effects of response-produced cost upon human observer responses during extinction following FI reinforcement. Relative to a no-cost condition, cost produced marked and rapid response attenuation.     

Resurgence following differential reinforcement of alternative behavior implemented with and without extinction

In the clinic, differential reinforcement of alternative behavior (DRA) often involves programming extinction for destructive behavior while reinforcing an alternative form of communication (e.g., a functional communication response); however, implementing extinction can be unsafe or impractical under some circumstances. Quantitative theories of resurgence (i.e., Behavioral Momentum Theory and Resurgence as Choice) predict differences in the efficacy of treatments that do and do not involve extinction of target responding when reinforcement conditions maintaining alternative responding worsen. We tested these predictions by examining resurgence following two DRA conditions in which we equated rates of reinforcement. In DRA without extinction, target and alternative behavior produced reinforcement. In DRA with extinction plus noncontingent reinforcement, only alternative behavior produced reinforcement. We conducted this study in a reverse-translation sequence, first with participants who engaged in destructive behavior (Experiment 1) and then in a laboratory setting with rats (Experiment 2). Across both experiments, we observed proportionally lower levels of target responding during and following the DRA condition that arranged extinction for the target response. However, levels of resurgence were similar following both arrangements.     

Persistence during and resurgence following noncontingent reinforcement implemented with and without extinction

Noncontingent reinforcement (NCR) is typically implemented with extinction (EXT) for destructive behavior reinforced by social consequences and without EXT for destructive behavior reinforced by sensory consequences. Behavioral momentum theory (BMT) predicts that responding will be more persistent, and treatment relapse in the form of response resurgence more likely, when NCR is implemented without EXT due to the greater overall rate of reinforcement associated with this intervention. We used an analogue arrangement to test these predictions of BMT by comparing NCR implemented with and without EXT. For two of three participants, we observed more immediate reductions in responding during NCR without EXT. However, for all participants, NCR without EXT produced greater resurgence than NCR with EXT when we discontinued all reinforcers during an EXT Only phase, although there was variability in response patterns across and within participants. Implications for treatment of destructive behavior using NCR are discussed.