The Role of Emotions in Reinforcement: Response Selection in Humans

The Psychological Record - Historically, researchers have never quite been able to agree as to the role of emotions, if any, when behavior is selected by its consequences. A brief review of...     

Reinforcement Delay Fading During Differential Reinforcement of Communication: The Effects of Signals on Response Maintenance

Signals during delays to reinforcement may lessen reductions in responding that typically occur when there is a delay between a response and its reinforcer. Sparse applied research has been devoted to understanding the conditions under which responding may be maintained when delays to reinforcement are introduced. We evaluated the extent to which providing signals during delay fading affected responding in the context of differential reinforcement of communication responses. Three individuals were exposed to gradually increasing signaled and unsignaled reinforcement delays in multiple‐schedule and/or withdrawal designs. Results for 2 of 3 participants suggested that (a) the presence of signals facilitated response maintenance under delayed reinforcement and (b) coordinated basic and applied research may advance both conceptual understanding and clinical outcomes of delayed reinforcement.     

Variable-Interval Schedule Control Following Response Acquisition with Delayed Reinforcement

The Psychological Record - Four experimentally naive White Carneau pigeons acquired a key-peck response without specific response shaping or other training when such responding was reinforced...     

Stimulus Fading and Response Elaboration in Differential Reinforcement for Alternative Behavior

A hallmark of applied behavior analysis is the development of function‐based interventions for problem behavior. A widely recommended function‐based intervention is differential reinforcement of alternative behavior (DRA), in which reinforcement is contingent upon socially acceptable alternatives to problem behavior (e.g., teaching communication skills). Typically, DRA is introduced under rich schedules of reinforcement. Although effective for initiating behavior change, rich schedules are often impractical in the natural setting. In this study, we evaluated the extent to which a stimulus fading program could be employed to elaborate alternative behavior (mands) in two individuals diagnosed with an autism spectrum disorder. For both participants, problem behavior was reduced substantially upon implementation of the DRA procedure. Further, problem behavior rates remained low and mand rates decreased to more practical levels as the DRA behavioral requirements increased during the fading program. The fading approach demonstrated in this paper may be a useful component of intervention packages for clinicians. Copyright © 2015 John Wiley & Sons, Ltd.     

Delayed Alternation to Non-Positional Cues in Chimpanzee

Three subjects were exposed to fixed-ratio schedules of reinforcement in a two-phase experiment. In the first phase, sessions were terminated after a fixed number of responses had been emitted. In the second phase, sessions were terminated after a fixed length of time (equivalent to the mean of session lengths when steady state responding occurred in Phase 1). A comparison of response rates showed higher rates for all subjects in Phase 2.     

Modulation of Response Timing in ADHD,Effects of Reinforcement Valence and Magnitude

The present study investigated the impact of reinforcement valence and magnitude on response timing in children with ADHD. Children were required to estimate a 1-s interval, and both the median response time (response tendency) and the intrasubject-variability (response stability) were investigated. In addition, heart rate and skin conductance were measured to examine the autonomic responses to reinforcement. Feedback-only trials were compared to low response cost trials (response cost for incorrect responses), low reward trials (reward for correct responses), high response cost and high reward trials. In feedback-only trials, children with ADHD underestimated more severely the interval and responded more variably than controls. Children with ADHD, unlike controls, were unaffected by the reinforcement conditions in terms of time underestimations. The variability of responding, on the other hand, decreased under conditions of reinforcement to a larger extent in children with ADHD than controls. There were no indications that children with ADHD were abnormally affected by the valence or magnitude of reinforcement. Furthermore, skin conductance responses increased when feedback was coupled with reinforcement, an effect which was larger in children with ADHD than controls. This could be interpreted as demonstrating that children with ADHD suffer from a diminished awareness of the significance of feedback in the feedback-only condition. The current study suggests that children with ADHD suffer from motivation problems when reinforcement was not available, at least when variability in responding was measured. Underestimations of time may reflect more stable deficits in ADHD.     

Chimpanzee gaze following in an object-choice task

Many primate species reliably track and follow the visual gaze of conspecifics and humans, even to locations above and behind the subject. However, it is not clear whether primates follow a human’s gaze to find hidden food under one of two containers in an object-choice task. In a series of experiments six adult female chimpanzees followed a human’s gaze (head and eye direction) to a distal location in space above and behind them, and checked back to the human’s face when they did not find anything interesting or unusual. This study also assessed whether these same subjects would also use the human’s gaze in an object-choice task with three types of occluders: barriers, tubes, and bowls. Barriers and tubes permitted the experimenter to see their contents (i.e., food) whereas bowls did not. Chimpanzees used the human’s gaze direction to choose the tube or barrier containing food but they did not use the human’s gaze to decide between bowls. Our findings allowed us to discard both simple orientation and understanding seeing-knowing in others as the explanations for gaze following in chimpanzees. However, they did not allow us to conclusively choose between orientation combined with foraging tendencies and understanding seeing in others. One interesting possibility raised by these results is that studies in which the human cannot see the reward at the time of subject choice may potentially be underestimating chimpanzees’ social knowledge. Received: 16 February 1998 / Accepted after revision: 5 July 1998     

Programming for Maintenance: An Investigation of Delayed Intermittent Reinforcement and Common Stimuli to Create Indiscriminable Contingencies

Generalization across time or maintenance of behavior change is a fundamental concern for behavior analysts and educators that remains insufficiently understood. This study examined the maintenance of mathematics responding during and following delayed intermittent reinforcement when common stimuli were programmed across the treatment and maintenance phases. Two third-grade girls who were referred by their classroom teacher due to concerns in the area of mathematics participated. Students were exposed to baseline, contingent reinforcement, delayed intermittent reinforcement, and a maintenance condition. The maintenance condition followed exposure to delayed intermittent reinforcement and included common stimuli from the reinforcement condition, but did not include a contingency for correct responding. Both students exhibited substantial prolonged maintenance during this condition. Implications of these results for future research examining maintenance and applied programming for maintenance are discussed.     

Recognition of Line-Drawing Representations by a Chimpanzee (Pan troglodytes)

The ability of a chimpanzee to recognize individuals portrayed in line drawings was evaluated. A 12-year-old female chimpanzee with extensive prior experience in the use of visual symbols matched the line drawings of chimpanzees, humans, and an orangutan with a specific letter of the alphabet. When a line drawing of a familiar individual was presented on the computer screen, the chimpanzee responded by punching a key with the letter of the alphabet that corresponded to the individual's name. Results indicate that the chimpanzee is able to categorize individuals from novel line-drawing representations.     

Intermittent reinforcement of a continuous response

Konorski showed that when a go/no-go procedure was used, sound quality discriminations were rapidly acquired and sound location discriminations were slowly acquired. These findings have been interpreted as a general constraint on the acquisition of auditory discriminations (quality-location effect). However, experiments carried out within an evolutionary framework (Harrison, 1984) have shown that the rate of acquisition of sound location discriminations varies widely as a function of the inclusion or exclusion of naturalistic features. These data suggest that Konorski's findings were a function of the special conditions of the experiments. The first purpose of the present experiments was to assess whether rats showed the effects noted by Konorski when studied under similar conditions. The second purpose was to study the effect of manipulating two natural features (novelty and stimulus-response adjacency) to assess whether the acquisition rates of quality and location discriminations could be greatly modified or made approximately equal, or both. When a go/no-go procedure was used and the other conditions were similar to those of Konorski, rats acquired a quality discrimination but did not acquire a location discrimination. However, when the S+ or S- were presented through a closely adjacent speaker, the sound location discrimination was acquired as rapidly as the quality discrimination. Finally, preexposing the animal to either S+ or S- retarded the rate of or prevented the acquisition of the quality discrimination. The experiments showed that the quality-location effect was determined primarily by the conditions used in Konorski's experiments, and that the effect is not a general constraint on learning.     

Response Interruption and Differential Reinforcement of Alternative Behavior for the Treatment of Pica

Pica displayed by two individuals with autism was decreased by a treatment involving differential reinforcement and response interruption that altered the chain of behavior involved in pica (i.e., picking up items and placing them in the mouth). The treatment involved establishing prompts to ‘clean‐up’ as a new discriminative stimulus (SD) for picking up items from the floor; and holding potential pica items was established as an SD for discarding those items in a trash receptacle, putting them away, or using them appropriately. After demonstrating the effectiveness of the treatment in an analog setting, the treatment package was systematically generalized to community settings. Copyright © 2011 John Wiley & Sons, Ltd.     

Effects Of Histories Of Differential Reinforcement Of Response Rate On Variable-interval Responding

Three pigeons were exposed first to multiple differential-reinforcement-of-high-rate and differential-reinforcement-of-low-rate schedules that were correlated with green and red keys, respectively, and then were shifted to a variable-interval schedule arranged on a white key. In subsequent test sessions, the variable-interval schedule continued to operate, but green and red keys replaced the white key in alternate sessions. In Part 1 of the experiment, the variable-interval schedule correlated with the white key was introduced immediately after the multiple-schedule condition, and the test condition began 15 days later. This sequence was repeated twice, with a reversal of the correlation of the key colors with the components of the multiple schedule at the start of each new cycle. Part 2 added a 6-month break between the multiple-schedule history and the white-key variable-interval schedule followed by test sessions. The procedure was then repeated with a reversal of the correlation between key colors and multiple-schedule components. In the test sessions of Part 1, all pigeons consistently responded faster in the presence of the key color most recently correlated with the differential-reinforcement-of-high-rate contingency than during the color most recently correlated with the differential-reinforcement-of-low-rate contingency. Similar but smaller effects were observed in Part 2. The effects of the reversals in these two parts of the experiment showed that only the most recent contingency exerted an influence on subsequent responding. The data suggest that this effect of the most recent history continues to operate on behavior under current contingencies even after a long lapse of time.     

Reinforcement and punishment in a closed system

Children chose between toys freely and with various restrictive contingencies. Sometimes play with a preferred toy was contingent on play with a nonpreferred toy. Sometimes play with a nonpreferred toy was contingent on play with a preferred toy. Another toy (free toy) was always available during contingency sessions. Because toy playing occupied the entire session the response system was closed. When one response increased in duration others had to decrease. An analysis of closed-system responding revealed that the restrictions of the closed system together with the restrictions imposed by the contingencies forced subjects to alter the proportion of time devoted to the three responses. A geometrical model representing the closed system and an analytical method based on distance are presented to describe the data.