DRA contingencies promote improved tolerance to delayed reinforcement during FCT compared to DRO and fixed-time schedules

Following Functional Communication Training (FCT), clinicians often gradually expose newly taught communicative responses to delayed reinforcement contingencies to prepare clients for the normative environment in which requests are frequently reinforced after a delay. The introduction of delays may result in the resurgence and maintenance of problem behavior and the weakening of the newly trained communicative response. The current study compared delay tolerance with three individuals diagnosed with intellectual and developmental disabilities when reinforcement for the functional communication response (FCR) was delivered following (a) the passage of time, (b) the omission of problem behavior, or (c) the occurrence of an alternative behavior. We measured delay tolerance in terms of minimizing problem behavior and maintaining efficient FCRs. Outcomes support requiring alternative responding during delays to attain optimal treatment results.     

Choice patterns reveal qualitative individual differences among discounting of delayed gains,delayed losses,and probabilistic losses

A new probabilistic losses questionnaire as well as Kirby's delayed gains questionnaire and a previously developed delayed losses questionnaire were administered to a large online sample. Almost all participants showed the positive discounting choice pattern expected on the Kirby questionnaire, decreasing their choice of a delayed gain as time to its receipt increased. In contrast, approximately 15% of the participants showed negative discounting on the delayed losses questionnaire and/or the probabilistic losses questionnaire, decreasing their choice of an immediate loss as time to a delayed loss decreased and/or decreasing their choice of a certain loss as likelihood of the probabilistic loss increased. Mixture model analysis confirmed the existence of these negative discounting subgroups. The inconsistent findings observed in previous research involving delayed/probabilistic losses may be due to differences in the proportion of negative discounters who participated in previous studies. Further research is needed to determine how negative discounting of delayed and probabilistic losses manifests itself in everyday decisions. It should be noted that the presence of individuals who show atypical choice patterns when losses are involved may pose challenges for efforts to modify discounting in order to ameliorate behavioral problems, especially because many such problems concern choices that have negative consequences, often delayed and/or probabilistic.     

胆道术后胃功能性排空障碍治疗体会

探讨胆道术后胃功能性排空障碍的诊治经验。回顾性分析32例胆道术后胃功能性排空障碍病例。结果32例胃功能性排空障碍发生于术后5天～10天,经保守治疗后均痊愈。胆道术后胃功能性排空障碍是胃的功能性病变,经综合保守治疗是可以治愈的。     

Reversing the Signaled Magnitude Effect in Delayed Matching to Sample: Delay-specific Remembering

Pigeons performed a delayed matching‐to‐sample task in which large or small reinforcers for correct remembering were signaled during the retention interval. Accuracy was low when small reinforcers were signaled, and high when large reinforcers were signaled (the signaled magnitude effect). When the reinforcer‐size cue was switched from small to large partway through the retention interval, accuracy accordingly changed from low to high. The opposite happened when the cue was switched from large to small. This dissociation of forgetting from the passage of time raises the possibility that remembering is delay‐specific. The reversal of the signaled magnitude effect during the retention interval is consistent with an attentional account in which the stimulus control of remembering is influenced by extraneous events.     

Short-term memory for responses: the "choose-small" effect

Pigeons' short-term memory for fixed-ratio requirements was assessed using a delayed symbolic matching-to-sample procedure. Different choices were reinforced after fixed-ratio 10 and fixed-ratio 40 requirements, and delays of 0, 5, or 20 s were sometimes placed between sample ratios and choice. All birds made disproportionate numbers of responses to the small-ratio choice alternative when delays were interposed between ratios and choice, and this bias increased as a function of delay. Preference for the small fixed-ratio alternative was also observed on "no-sample" trials, during which the choice alternatives were presented without a prior sample ratio. This "choose-small" bias is analogous to results obtained by Spetch and Wilkie (1983) with event duration as the discriminative stimulus. The choose-small bias was attenuated when the houselight was turned on during delays, but overall accuracy was not influenced systematically by the houselight manipulation.     

Use of an ambiguous-sample procedure to establish a cue to forget in pigeons

Pigeons were trained on a variation of the matching-to-sample task in which on double-sample trials two samples, one associated with each of the comparison stimuli, were presented successively. Responding to the comparison associated with the first sample was reinforced on half the double-sample trials, and responding to the comparison associated with the second sample was reinforced on the remaining half. One of two postsample stimuli was presented following the termination of each colored sample. A vertical line was presented after a correct or target sample, and a horizontal line was presented after an incorrect or interfering sample. With extended training, each bird demonstrated above-chance accuracy on double-sample trials, providing prima facie evidence that one or both of the postsample stimuli exerted control over matching behavior. Experiment 2 provided evidence that the horizontal line functioned as a cue to forget the code activated by the preceding sample stimulus. It was concluded that a condition sufficient to establish a postsample stimulus as a cue to forget is that the postsample immediately follow presentation of a sample that, if it were to control test responding, would lead to nonreinforcement.     

Operant hoarding: a new paradigm for the study of self-control.

In the first of four experiments, rats were exposed to a modified multiple continuous reinforcement-extinction schedule during 15-min daily sessions. In one condition (saves condition) with the cuelight on, a single lever press produced a food pellet, briefly extinguished the cuelight, and started a clock. Saves (additional lever presses with interresponse times less than 1 s) produced an additional food pellet, briefly extinguished the cuelight, and restarted the interresponse time clock. The cuelight was extinguished 1 s after the last lever press and remained off during a 10-s period of extinction, during which no food pellets were delivered. In the other condition (savings account condition), the contingencies were the same except that the cuelight was extinguished and was not reilluminated after the initial lever press, and the delivery of all food pellets in the reinforcement component was delayed until the onset of extinction. In both conditions, rats made saves, but mean saves (total saves divided by the number of reinforcement components) were slightly reduced in the savings account condition. In Experiment 2, using six equally spaced 15-min sessions per day on alternate days, saves were either followed immediately with food and brief cuelight offset (saves condition) or were not reinforced at all. Mean saves were much greater when saves were reinforced. In Experiment 3, during 5-min daily sessions, saves earned a single pellet (savings account condition) or a number of pellets equal to the ordinal number of the lever press (interest condition). Rats made fewer mean saves, with little change in the food rate, when saves earned interest. In Experiment 4, the rats earned all their food in the operant situation during 24 daily 5-min sessions, these separated by 55-min intersession intervals during which no food was available; otherwise, the conditions were the same as in Experiment 3. In Experiment 4, the shift to interest for saves led to an increase in mean daily mean saves (total daily mean saves divided by the number of daily sessions) as well as to an increase in the number of food pellets delivered in each session. The results are discussed in terms of self-control and behavioral economics.     

Verbal self-reports of delayed matching to sample by humans

Undergraduates participated in two experiments to develop methods for the experimental analysis of self-reports about behavior. The target behavior was the choice response in a delayed-matching-to-sample task in which monetary reinforcement was contingent upon both speed and accuracy of the choice. In Experiment 1, the temporal portion of the contingency was manipulated within each session, and the presence and absence of feedback about reinforcement was manipulated across sessions. As the time limits became stricter, target response speeds increased, but accuracy and reinforcement rates decreased. When feedback was withheld, further reductions in speed and reinforcement occurred, but only at the strictest time limit. Thus, the procedures were successful in producing systematic variation in the speed, accuracy, and reinforcement of the target behavior. Experiment 2 was designed to assess the influence of these characteristics on self-reports. In self-report conditions, each target response was followed by a computer-generated query: “Did you earn points?” The subject reported by pressing “Yes” or “No” buttons, with the sole consequence of advancing the session. In some cases, feedback about reinforcement of the target response followed the reports; in other cases it was withheld. Self-reports were less accurate when the target responses occurred under greater time pressure. When feedback was withheld, the speed of the target response influenced reports, in that the probability of a “Yes” report increased directly with the speed of accurate target responses. In addition, imposing the self-report procedure disrupted target performance by reducing response speeds at the strictest time limit. These results allow investigation of issues in both behavioral and cognitive psychology. More important, the overall order in the data suggests promise for the experimental analysis of self-reports by human subjects.     

Short-term memory in the pigeon: relative recency

Three pigeons pecked for food in an experiment in which each trial consisted of two phases. The first phase consisted of a pattern of three successively illuminated, randomly selected left or right keys. A subject was required to peck each of the lighted keys as they appeared. Thus, in the first phase, a subject emitted a pattern of three left- or right-key pecks. Over trials, all eight possible patterns appeared. A time interval separated the first phase from the second phase, which began with presentation of a randomly selected one of three cues. A reinforcer was delivered in the second phase if a subject pecked the side key that had appeared in the first phase in an ordinal position corresponding to the cue presented in the second phase. That is, the three cues probed a pigeon's memory for the side key it had pecked first, second, or third, in the first phase of a trial. The results show that a pigeon can remember for more than 4 sec the order in which it has just seen and pecked two lighted keys: a pigeon can remember the temporal organization or pattern of events in its recent environment. Consequently, the functional stimulus present when a reinforcer is delivered may include a subject's short-term memory for the temporal organization of recent events, such as the pattern of its own recent behavior. This possibility is consistent with a molecular analysis of operant behavior focusing on local patterns of behavior.