Discriminative stimulus control and the effects of concurrent operants.

Discriminative-stimulus-control functions were investigated in a concurrent operant context. Variable-interval reinforcement schedules were arranged for pigeons on two response keys. One key, illuminated with a white vertical line on green background (position irrelevant), was programmed with a given schedule value across groups. For different groups of pigeons, the alternative key, illuminated with green alone, was programmed with twice, the same, or half the reinforcement frequency of the other key. Stimulus-control gradients were collected from both keys as line orientation was varied. On the green-plus-line alternative, flattest gradients were observed when twice the reinforcement frequency was concurrently programmed and the steepest were observed when equal values were concurrently programmed. Also examined were the effects of a programmed changeover delay, important in maintaining the independence of concurrent operants. The changeover delay was found to have relatively minor effects upon stimulus control, despite its typical and marked effects upon steady-state responding.     

Molar optimization versus delayed reinforcement as explanations of choice between fixed-ratio and progressive-ratio schedules.

In a discrete-trials procedure, pigeons chose between a fixed-ratio 81 schedule and a progressive-ratio schedule by making a single peck at the key correlated with one or the other of these schedules. The response requirement on the progressive-ratio schedule began at 1 and increased by 10 each time the progressive-ratio schedule was chosen. Each time the fixed-ratio schedule was chosen, the requirement on the progressive-ratio schedule was reset to 1 response. In conditions where there was no intertrial interval, subjects chose the progressive-ratio schedule for an average of about five consecutive trials (during which the response requirement increased to 41), and then chose the fixed-ratio schedule. This ratio was larger than that predicted by an optimality analysis that assumes that subjects respond in a pattern that minimizes the response-reinforcer ratio or one that assumes that subjects respond in a pattern that maximizes the overall rate of reinforcement. In conditions with a 25-s or 50-s intertrial interval, subjects chose the progressive-ratio schedule for an average of about eight consecutive trials before choosing the fixed-ratio schedule. This change in performance with the addition of an intertrial interval was also not predicted by an optimality analysis. On the other hand, the results were consistent with the theory that choice is determined by the delays to the reinforcers delivered on the present trial and on subsequent trials.     

NEGATIVE REINFORCEMENT IN APPLIED BEHAVIOR ANALYSIS: AN EMERGING TECHNOLOGY

Although the effects of negative reinforcement on human behavior have been studied for a number of years, a comprehensive body of applied research does not exist at this time. This article describes three aspeas of negative reinforcement as it relates to applied behavior analysis: behavior acquired or maintained through negative reinforcement, the treatment of negatively reinforced behavior, and negative reinforcement as therapy. A consideration of research currently being done in these areas suggests the emergence of an applied technology on negative reinforcement.     

The efficacy of all-positive management as a function of the prior use of negative consequences

Previous work suggests that an all-positive approach to child management can be effective. The present investigation extends these findings by examining the efficacy of an enhanced all-positive management system in the absence of a history of negative consequences. The on-task behavior and academic performance of 8 first- through third-grade children with academic and/or behavioral problems were observed in the classroom. Results indicated that, in the absence of a history of negative consequences, enhanced positive consequences were not sufficient to maintain on-task rates or academic accuracy at acceptable levels. The addition of negative consequences resulted in an immediate increase in on-task behavior and academic accuracy; a primarily positive approach appeared to be successful in maintaining these gains following the gradual (as opposed to abrupt) removal of the negative consequences.     

Self-stimulatory behavior and perceptual reinforcement.

Self-stimulatory behavior is repetitive, stereotyped, functionally autonomous behavior seen in both normal and developmentally disabled populations, yet no satisfactory theory of its development and major characteristics has previously been offered. We present here a detailed hypothesis of the acquisition and maintenance of self-stimulatory behavior, proposing that the behaviors are operant responses whose reinforcers are automatically produced interoceptive and exteroceptive perceptual consequences. The concept of perceptual stimuli and reinforcers, the durability of self-stimulatory behaviors, the sensory extinction effect, the inverse relationship between self-stimulatory and other behaviors, the blocking effect of self-stimulatory behavior on new learning, and response substitution effects are discussed in terms of the hypothesis. Support for the hypothesis from the areas of sensory reinforcement and sensory deprivation is also reviewed. Limitations of major alternative theories are discussed, along with implications of the perceptual reinforcement hypothesis for the treatment of excessive self-stimulatory behavior and for theoretical conceptualizations of functionally related normal and pathological behaviors.     

USE OF NEGATIVE REINFORCEMENT IN THE TREATMENT OF SELF-INJURIOUS BEHAVIOR

Behavioral assessment procedures were used to determine the maintaining conditions of self-injury exhibited by 2 children with severe multiple handicaps. For both children, negative reinforcement (escape from grooming activities) was determined to be the maintaining reinforcer for self-injury (hand/arm biting) within an alternating treatments design. The treatment packages involved the use of negative reinforcement (brief escape from grooming activities) contingent upon a behavior that was incompatible with self-injury (reaching and pressing a microswitch that activated a prerecorded message of “stop”). Treatment was evaluated with a reversal design for 1 child and with a multiple baseline across grooming activities for the 2nd child. The treatment led to a marked decrease in self-injury for both children. At follow-up, high rates of self-injury were reported for the 1st child, but low rates of self-injury and an increase in task-related appropriate behavior were observed for the 2nd child.     

EFFECTS AND SIDE EFFECTS OF DRO AS TREATMENT FOR SELF-INJURIOUS BEHAVIOR

A three-part controlled case study is presented in which severe and longstanding self-injurious behavior exhibited by a 9-year-old-boy was treated successfully with differential reinforcement of other behavior. In Phase 1, an experimental analysis demonstrated that the boy's scratching was not maintained by environmental contingencies; instead, it appeared that the self-injurious behavior was a stereotypic (automatically reinforced) response. In Phase 2, the effects of an escalating differential-reinforcement-of-other-behavior schedule mediated through token reinforcement (pennies) were evaluated in a reversal design. Results showed that differential-reinforcement-of-other-behavior eliminated self-injurious behavior very quickly and for periods of time as long as 30 min. A noteworthy side effect observed during Phase 2 was the occurrence of crying behavior following the nondelivery of reinforcement. In Phase 3, the token program was gradually extended in 30-min increments throughout the day. Additionally, results of a brief multielement manipulation showed that the effects of token reinforcement were superior to those of a more easily administered differential reinforcement of other behavior based on social reinforcement, which differed little from baseline.     

Temporal patterns of responding in small fixed-ratio schedules

Pigeons were exposed to an ascending series of small fixed-ratio schedules from fixed-ratio 1 to 7. Two of those pigeons were later placed on a fixed-ratio 30 schedule. The two primary dependent variables were the postreinforcement pause and the interresponse time. Changes in these variables under small fixed ratios were sometimes opposite to changes reported with large fixed ratios. For example, postreinforcement pauses decreased in length as the fixed-ratio requirement increased from fixed-ratio 1 to fixed-ratio 3. Also, the interresponse times early in the small fixed-ratio schedule were shorter than those immediately preceding reinforcement. These findings question the role of interresponse-time reinforcement in determining temporal patterns of responding under small fixed-ratio schedules. They also suggest that there may be a limited region in which the independent variable, fixed-ratio size, does not operate as previously described.     

Sensitivity of time allocation to concurrent-schedule reinforcement

Four pigeons were trained on concurrent variable-interval schedules programmed on a center response key, with access to those schedules controlled by responses on left or right side keys. Two procedures were used. In one, the pigeon was given limited access, in that each side-key response produced 3-s access to a center-key schedule, and in the other procedure, access was unlimited. Data were analyzed using the generalized matching law. Comparison of sensitivities to reinforcement of interchangeover time for both procedures showed them to be of similar magnitude. Response sensitivities were also similar in magnitude for both procedures. From the limited-access procedure a second time measure that was available, switched-in time, was relatively uncontaminated by time spent emitting behavior other than key pecking. Sensitivities to reinforcement for the switched-in time measure were always smaller than interchangeover-time sensitivities for either procedure, and were approximately equal to response sensitivities for the limited-access procedure. Two other access times (5 and 7.5 s) were studied to validate the choice of 3 s as the main access time. These results indicate that when time spent emitting other behavior is excluded from interchangeover time, time and response sensitivities will be approximately equal.     

Component probability and component reinforcer rate as biasers of free-operant detection

Six pigeons were trained on multiple schedules whose components were concurrent variable-interval extinction and concurrent extinction variable-interval schedules. In Experiments 1a and 1b the stimuli signaling the components were two different light intensities, and in Experiments 2a and 2b they were two identical intensities. The components of the multiple schedule changed probabilistically after each reinforcer. In Experiments 1a and 2a, the probability of presenting the components was varied over five conditions and a replication. In Experiments 1b and 2b, the component probability was .5 and the component reinforcer rates were varied systematically over five conditions and a replication. The data, analyzed according to the Davison-Tustin behavioral detection model, confirmed that the discriminability of the stimuli signaling the components was high when the stimuli were different, and low when the stimuli were the same. Discriminability, measured by log d, was unaffected by component probability variation and by component reinforcer-rate variation. When discriminability was high, bias, or the response allocation between the two keys, was more strongly affected by variation of reinforcer rate within components than by variation of component probability, but the reverse was found when discriminability was low. The results suggest that free-operant detection performance is controlled by the rates of reinforcers in periods of time in which stimuli signal differential contingencies. These periods comprise the components when the component stimuli are discriminable, and comprise the total session when the components are indiscriminable. An extension of the Davison-Tustin behavioral detection model that incorporates these results is presented.