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M N Branch

Publications and source records attributed to M N Branch.

43 records · Page 3Linked to original sources

Signalled and unsignalled percentage reinforcement of performance under a chained schedule.

Pigeons were trained to peck a key under a chained fixed-ratio 15 fixed-interval 25-sec schedule of food presentation. In Experiment 1, blocks of sessions in which 100%, 75%, 50%, and 25% of the sequences ended with food presentation were conducted. When food presentation was omitted, a timeout of equal duration replaced it. As the frequency of food presentation decreased so did the frequency of completing the chained schedule. In Experiment 2, 75%, 50%, or 25% of the sequences terminated with food presentation and outcomes were signalled, i.e., completion of the fixed ratio resulted in either a stimulus correlated with the fixed-interval 25-sec schedule or a stimulus correlated with extinction. As the frequency of food presentation decreased, the number of sequences completed per session increased for two pigeons and remained high for a third. In Experiments 3 and 4, assessments of the effects of signalling the outcome of the chained schedule were made with response-independent presentation of events at the end of the sequence. Again, signalling the outcome of the chained schedule led to more chains being completed per session than did not signalling the outcome. Stimuli differentially paired with food presentation have powerful behavioral effects that may be attributed to the potency of these stimuli as conditioned reinforcers.

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On the role of "memory" in the analysis of behavior.

Shimp's (1976) recent paper on memory and the structure of behavior is discussed, as is the concept of memory itself. Radical behaviorism is distinguished from associationism, and behavioral accounts of experiments on short-term and long-term memory are provided. Unobservable theoretical quantities, such as rate of response, are distinguished from theoretical constructs such as memory. The logical inconsistency involved in the use of short-term memory as a "theoretical primitive" in the definition of units of behavior is explicated, and an alternative strategy for identifying units of behavior is presented. It is argued that the experimental analysis of behavior has ignored processes usually considered as memorial because many of the phenomena are irreversible. Methods for the study of transitions in single subjects should be developed more fully. Possible pitfalls associated with subscription to the term memory are listed, and it is concluded that the concept is neither required nor helpful in the analysis of behavior.

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Punishment-specific effects of pentobarbital: dependency on the type of punisher.

Pigeons were trained to peck a key under a multiple random-interval 1-minute, random-interval 6-minute schedule of food presentation. Subsequently, over three phases, additions were made during the random-interval 1-minute component as follows: pecks during the component occasionally were punished by timeout presentation (Phase 1), timeouts were presented independently of responding during the component (Phase 2), pecks during the component occasionally were punished by electric-shock presentation (Phase 3). In Phases 1 and 3, response-dependent timeout and shock suppressed responding and established equivalent rates in both components of the multiple schedule. Intermediate doses of pentobarbital increased responding suppressed by electric-shock punishment but had little or no effect on responding suppressed by timeout punishment. Response-independent presentation of timeouts did not result in suppression of responding (thus showing that response-dependent timeout acted as a punisher), and pentobarbital did not reliably increase unpunished responding. Pentobarbital's selective "punishment-attenuating" properties depend on the nature of the punisher.

Animals↗

Effects of chlorpromazine and d-amphetamine on observing responses during a fixed-interval schedule.

Pigeons were trained to peck a response key that briefly produced stimuli correlated with the passage of time in a fixed-interval schedule of food presentation for pecks on another response key. Pecks on the key that produced food were not likely near the end of each fixed interval, whereas pecks on the key that produced the discriminative stimuli were most likely to occur during the middle portion of each fixed interval. Chloropromazine (3.0--30.0 mg/kg) and d-amphetamine (0.03--3.0 mg/kg) produced inverted U-shaped dose-effect curves with response rate on the food-producing key as the dependent variable, and monotonically decreasing functions were obtained for the discriminative-stimulus producing responses. A "rate-dependency" interpretation adequately described the drug effects on the temporal distributions of pecks on the food-producing key, but was not consistent with the disruption of the temporal distribution of pecks on the key that produced the discriminative stimuli. The pecks on the discriminative-stimulus producing key had some of the properties of schedule-induced, or adjunctive, behavior. The effects of amphetamine and chlorpromazine on the rate of adjunctive behaviors may not be predictable from control rates.

Animals↗

A detailed analysis of the effects of d-amphetamine on behavior under fixed-interval schedules.

Pigeons were exposed to fixed-interval schedules of food reinforcement with durations of 300 sec, 100 sec, or 40 sec. A range of doses of d-amphetamine was administered to each pigeon, and the resulting behavior was analyzed at several levels of detail. Average rates in different portions of the intervals predicted the magnitude of the drug's effect, but a finer analysis showed that average rates did not adequately characterize the behavior in some parts of the intervals. The probability of responding in different parts of an interval without drug was also a good predictor of the magnitude of the effect of d-amphetamine, and at the same time was more descriptive of the interval-to-interval performance. Analyses of the control performance indicated that responding in individual intervals could be described as consisting of two parts: a very low, or zero, rate at the beginning of the interval followed by an abrupt transition to a slightly, but reliably, positively accelerated rate maintained until reinforcement.

Animals↗

Observing responses in pigeons: effects of schedule component duration and schedule value.

Pigeons were exposed to a procedure under which five pecks on one response key (the observing key) changed the schedule on a second key (the food key) from a mixed schedule to a multiple schedule for 25 sec. In Experiment I, a random-ratio 50 schedule alternated with extinction. The duration of the random-ratio 50 schedule component was varied between 1.25 and 320 sec, and extinction was scheduled for a varying time, ranging from the duration of the random-ratio 50 to four times that value. Each set of values was scheduled for a block of sessions. Before observing-key pecks were allowed at each set of parameter values, the pigeons were exposed to a condition where the mixed and multiple schedule alternated every 10 min, and observing-key pecks were not permitted. Rates of pecking on the observing key were high for all values of random-ratio component durations except 1.25 sec. Experiment II was conducted with the random-ratio component duration equal to 40 sec, and the random-ratio schedule was varied from random-ratio 50 to 100, 200, and 400. Observing-key pecking rates were high for all values of the random-ratio schedule except random-ratio 400. In both experiments, observing response rates were relatively little affected, suggesting that neither schedule component duration nor schedule value is a strong determinant of observing responses.

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