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1.
The effects of different schedule requirements at reinforcement on patterns of responding by pigeons were assessed under conjunctive schedules with comparable response-number requirements, Under one conjunctive schedule (conjunctive fixed-interval fixed-ratio schedule), a response was reinforced after a 6-min interval had elapsedand a specific minimum number of responses had been emitted, Under a second conjunctive schedule, a response was reinforced after the 6-min fixed interval and upon completion of a tandem schedule requirement (conjunctive fixed-interval tandem schedule), This schedule retained the same required minimum number of responses as the first conjunctive schedule, but responses were never reinforced according to a fixed-ratio schedule; the tandem schedule was comprised of a fixed-ratio and a small (.1 to 10.0 sec) fixed-interval schedule, Under the conjunctive fixed-interval fixed-ratio schedule, responding was characterized by an initial pause, an abrupt transition to a high response rate, and a second transition to a lower rate that prevailed or slightly increased up to reinforcement, Under the conjunctive fixed-interval tandem schedule, pauses were extended, response rates were lower, and the initial high rate of responding was generally absent, The above effects depended upon the size of the fixed interval of the tandem schedule, The distinct pattern of responding generated by conjunctive fixed-interval fixed-ratio schedules depends upon occasional reinforcement of fixed-ratio responding and not merely on the addition of a minimum number of required responses. 相似文献
2.
The aim of the four present experiments was to explore how different schedules of reinforcement influence schedule-induced
behavior, their impact on evaluative ratings given to conditioned stimuli associated with each schedule through evaluative
conditioning, and the transfer of these evaluations through derived stimulus networks. Experiment 1 compared two contrasting
response reinforcement rules (variable ratio [VR], variable interval [VI]). Experiment 2 varied the response to reinforcement
rule between two schedules but equated the outcome to response rate (differential reinforcement of high rate [DRH] vs. VR).
Experiment 3 compared molar and molecular aspects of contingencies of reinforcement (tandem VIVR vs. tandem VRVI). Finally,
Experiment 4 employed schedules that induced low rates of responding to determine whether, under these circumstances, responses
were more sensitive to the molecular aspects of a schedule (differential reinforcement of low rate [DRL] vs. VI). The findings
suggest that the transfer of evaluative functions is determined mainly by differences in response rate between the schedules
and the molar aspects of the schedules. However, when neither schedule was based on a strong response reinforcement rule,
the transfer of evaluative judgments came under the control of the molecular aspects of the schedule. 相似文献
3.
We explored response rate as a possible mediator of learned stimulus equivalence. Five pigeons were trained to discriminate
four clip art pictures presented during a 10-sec discrete-trial fixed interval (FI) schedule: two paired with a one-pellet
reinforcer, which supported a low rate of responding, and two paired with a nine-pellet reinforcer, which supported a high
rate of responding. After subjects associated one stimulus from each of these pairs with a discriminative choice response,
researchers presented two new clip art stimuli during a 10-sec FI: one trained with a differential reinforcement of low rate
schedule (DRL) after the FI and the other trained with a differential reinforcement of high rate schedule (DRH) after the
FI. Each of the stimuli that were withheld during choice training was later shown to see if the choice responses would transfer
to these stimuli. The results suggest that response rate alone does not mediate learned stimulus equivalence. 相似文献
4.
This study presents a theory by which to understand how pigeons learn response patterns in simple choice situations. The theory assumes that, in a choice situation, patterns of responses compete for the final common path; that the competition is governed by two variables, the overall reinforcement probability obtained by emitting the patterns,T, and the differences in reinforcement probabilities among the patterns,D; and that the ratioD/T determines the final strength of specific response patterns. To test these predictions, three experiments were run in which pigeons were more likely to receive food when they pecked the momentarily least-preferred of three response keys. On the basis of previous research, it was predicted that the birds would be indifferent among the keys (molar aspect) and would also acquire a response pattern that consisted of pecking each key once during three consecutive trials (molecular aspect). The present theory went further and predicted that the strength of that pattern would increase with the ratioD/T. In the first two experiments,D was manipulated whileT remained constant, and in the third,T was manipulated whileD remained constant. The results agreed with the theory, for the strength of the response pattern increased withD and decreased withT, whereas overall choice proportions were always close to the matching equilibrium. 相似文献
5.
A reinforcement schedule states a rule for obtaining reinforcement as a function of behavior actually emitted and perhaps as a function of additional variables. These functions are here called “feedback functions.” Behavior actually emitted is, in turn, a function of obtained reinforcement. This reciprocal interdependency was quantified for an experiment in which pigeons chose among either three or two alternatives. Shifting from three to two alternatives, and vice versa, produced changes in the distribution of responding which were approximately accounted for by equations that combined the feedback functions with the matching law for reinforced responding. These equations predicted, among other things, a violation of the constant-ratio rule of formal choice theory and an absence of simultaneous contrast effects between response alternatives reinforced on variable-interval schedules. Both predictions were approximately confirmed. 相似文献
6.
Pigeons’ choice responding on 10-sec interpolated probes was studied after baseline training on multiple variable-interval variable-interval schedules of food reinforcement. Unreinforced choice following training with three different relative reinforcement rates (Experiment 1), with a 3-ply multiple schedule (Experiment 2), and with three different relative reinforcement durations (Experiment 3) was examined. Least squares lines were fit to choice relative response rate and schedule relative response rate as functions of training relative reinforcement rate; choice slope was significantly greater than schedule slope in all three experiments. This result is counter to the prediction of Herrnstein’s (1970) theory that these slopes should not differ. Luce’s (1959) theory also failed to account for the data. It was concluded that choice responding was controlled by both approach to the stimulus associated with the smaller mean interreinforcer interval or the longer duration, and avoidance of the other stimulus. 相似文献
7.
Four pigeons pecked for food reinforcement on variable interval 1-min schedules and on the variable-interval 1-min components of multiple, concurrent, and pseudoconcurrent schedules. The pseudoconcurrent schedule provided only one schedule of reinforcement; but, any reinforcer could be collected by responding on either of two keys. The rate of responding generated by the variable interval schedule was not greater than the rates of responding generated by the components of the complex schedules. But, the rate of reinforcement obtained from the variable interval schedule was greater than the rates of reinforcement obtained from the components of the multiple schedule. These results may contradict the equation proposed by Herrnstein (1970). The equation predicts that the rate of responding generated by a schedule of reinforcement will be greater when the schedule appears alone, than when it appears as one component of a complex schedule. 相似文献
8.
9.
Louis D. Matzel 《Learning & behavior》1985,13(2):187-193
A series of experiments used food-deprived pigeons to examine several parameters of reinforcement omission in an attempt to control changes of keypeck response measures on a subsequent schedule. In Experiments 1 and 2, the pigeons were tested with a multiple fixed-ratio schedule on which reinforcement was occasionally omitted at the completion of the first component. The duration of the delay occurring in lieu of reinforcement was systematically varied. In Experiment 3, the stimulus that signaled the second component of the schedule was altered to appear either more or less similar to the stimulus that signaled the first component. Two principal results are reported: (1) Response latency decreased and, to a much lesser extent, terminal response rate increased as the delay occurring in lieu of reinforcement decreased; and (2) both latency decrease and response-rate increase were enhanced by a second component stimulus which was similar to the first. The results are evaluated in terms of Amsel’s frustration theory and an analysis by Staddon which suggests that reinforcement inhibits responding. The data appear to support Staddon’s argument that rate increases and latency decreases following reinforcement omission are largely a function of an attenuation of the inhibitory influence of reinforcement, an effect that is enhanced by stimulus generalization. Accordingly, it is proposed that an animal’s response to reinforcement omission is determined by a stimulus complex that minimally includes the omission event and component cues. 相似文献
10.
In two experiments, we assessed whether rats optimize the number of reinforcers per response. In Experiment 1, one group of rats was trained to leverpress for food reinforcement on a simple variable-interval (VI) 60-sec schedule. For another group, a negative fixed-ratio component was imposed on the VI schedule to produce a conjoint contingency in which reinforcement became available on the VI schedule but was omitted when the ratio criterion was satisfied. In Experiment 2, one group of rats responded on a VI schedule and also received response-independent food. For another group, responding above a certain rate canceled the response-independent food. Despite the negative contingency experienced by the groups in Experiments 1 and 2, responding was maintained at a level at which the number of obtained reinforcers was reduced substantially below the maximum number possible. In addition, in both experiments, the groups that experienced the negative contingency responded at a lower rate than did a yoked control group that experienced the same frequency of reinforcement but lacked the negative component. These results demonstrate that although rats do not optimize their behavior with respect to reinforcement, they are nevertheless sensitive to some aspect of the instrumental contingency in operation. 相似文献
11.
Four pigeons were exposed to several nonindependent concurrent variable-interval schedules of reinforcement. One schedule component required a keypecking response; the other component required a treadlepressing response. The birds matched the ratio of their behavior (as measured by responses and time) between the two topographically different responses to the ratio of reinforcement in those two components. When additional foods not contingent on a keypeck or treadle-press were then added, the birds matched time spent in the components to total rates of food delivered in those components; response matching was somewhat disrupted. The matching law, developed under concurrent variable-interval schedules requiring similar responses, can thus account for choice behavior involving topographically different responses. 相似文献
12.
In three experiments, we examined the effects of signaling reinforcement during operant responding in order to illuminate the factors underlying instrumental overshadowing and potentiation effects. Specifically, we examined whether signaling reinforcement produces an enhancement and attentuation of responding when the response-reinforcer correlation is weak and strong, respectively. In Experiment 1, rats responded on variable-ratio (VR) or variable-interval (VI) schedules that were equated for the number of responses emitted per reinforcer. A signal correlated with reinforcement enhanced response rates on the VR schedule, but attenuated response rates were produced by the signal on the VI schedule. In Experiment 2, two groups of rats responded on a VI schedule while the two other groups received a conjoint VI, negative fixed-ratio schedule in which the subjects lost the availability of reinforcements if they emitted high response rates. A reinforcement signal attenuated responding for the simple VI groups but not for the animals given the negative fixed-ratio component, although the signal improved response efficiency in both groups. In Experiment 3, a poor correlation between responding and reinforcement was produced by a VI schedule onto which the delivery of response-independent food was superimposed. A signal for reinforcement initially elevated responding on this schedule, relative to an unsignaled condition; however, this pattern was reversed with further training. In sum, the present experiments provide little support for the view that signaling reinforcement enhances responding when the response-reinforcer correlation is weak and attenuates responding when this correlation is strong. 相似文献
13.
If pigeons are trained on matching-to-sample with differential responding required to the two samples, there is evidence that
the differential responding can control comparison choice. We asked whether similar responding required at two different locations
could also serve as the basis for comparison choice. Pigeons were pretrained to report the location that they had pecked.
To reduce the likelihood that they could use the presence of differential proprioceptive cues at the time of their report,
a common response was required between the location response and the comparison choice. They were then given experience with
a conditional discrimination in which location of the comparison response varied randomly and was incidental to the choice
of comparison. On test trials, after the pigeons had made their comparison choice, they showed a significant tendency to choose
the appropriate test comparison when they were unexpectedly asked to report the location of their previous pecking response.
These results have implications for the demonstration of episodic-like memory in pigeons because they suggest that pigeons
have the capacity to recall, unexpectedly, specific details about their past experiences. 2007 Psychonomic Society, Inc. 相似文献
14.
15.
Bruce L. Brown Nancy S. Hemmes David A. Coleman Alison Hassin Eva Goldhammer 《Learning & behavior》1982,10(3):365-376
Control of pigeons’ keypecking by a stimulus-reinforcer contingency was investigated in the context of a four-component multiple schedule. In each of three experiments, pigeons were exposed to a schedule consisting of two two-component sequences. Discriminative stimuli identifying each sequence were present only in Component 1, which was 4, 6, or 8 sec in duration, while reinforcers could be earned only in Component 2 (30 sec in duration). Control by a stimulus-reinforcer contingency was sought during Component 1 by arranging a differential relation between Component 1 cues and schedule of reinforcement in Component 2. In Experiment 1, rate of keypecking during Component 1 varied with the presence and absence of a stimulus-reinforcer contingency. When a contingency was introduced, rate of keypecking increased during the Component 1 cue associated with the availability of reinforcement in Component 2. In Experiment 2, the stimulus-reinforcer contingency was manipulated parametrically by varying the correlation between Component 1 cues and Component 2 schedules of reinforcement. Responding in Component 1 varied as a function of strength of the stimulus-reinforcer contingency. The relatively high rates of Component 1 responding observed in Experiments 1 and 2 pose difficulties for conceptions of stimulus-reinforcer control based on probability of reinforcement. In these two experiments, the stimulus-associated probabilities of reinforcement in Component 1 were invariant at zero. An alternate dimension of stimulus-reinforcer control was explored in Experiment 3, in which Component 1 cues were differentially associated with delay to reinforcement in Component 2, while probability of reinforcement was held constant across components. When the stimulus-reinforcer contingency was in force, rate of responding in Component 1 varied inversely with delay to reinforcement in Component 2. In a quantitative analysis of data from Experiments 2 and 3, relative rate of responding during Component 1 was strongly correlated with two measures of relative delay to reinforcement. 相似文献
16.
Frances K. McSweeney 《Learning & behavior》1975,3(3):264-270
Five pigeons pecked for food reinforcement on several concurrent schedules. Their body weights were varied from 80% to 110% of their free-feeding weights. A number of predictions of the equations proposed by Herrnstein (1970) were tested. As predicted, the relative rate of responding equalled the relative rate of reinforcement for all subjects, on all schedules, at all body weights. And, as predicted, the overall rates of responding on the components of a concurrent schedule were slower than the local rates of responding on the components of an identical multiple schedule. Contrary to prediction, the total rate of responding generated by the concurrent schedules did not increase with increases in the total rate of reinforcement they provided. And, contrary to prediction, the k parameter did not remain constant, and the R0 parameter did not increase with increases in body weight. It was concluded that Herrnstein’s matching law and his interpretation of the m parameter are correct but that the interpretations of k and R0 require further investigation. 相似文献
17.
Pigeons were studied on multiple variable-ratio yoked-variable-interval schedules in which components had equal rates of food reinforcement and appeared equally often on each of two keys. Interpolated between component changes on the final multiple schedule were 10-sec probes in which both schedule stimuli were present, one on each key. During multiple schedule training, variable-ratio response rates were greater than yoked-variable-interval rates; however, response rate differences in the components were not a function of the mean ratio value for the 40-to-320-ratio range studied. During the choice probes, subjects responded more to the stimulus associated with the interval schedule than to the one associated with the ratio schedule. It was concluded that pigeons prefer interval schedules over equal reinforcement rate ratio schedules, because the former generate fewer responses per reinforcement. 相似文献
18.
In two experiments, food-deprived rat subjects leverpressed for food in three successive training phases. In the first phase of both experiments, rats were exposed to a multiple schedule, one component of which produced a high rate of response, and the other of which produced a lower rate of response (multiple random ratio [RR], random interval [RI] in Experiment 1, and multiple differential reinforcement of high rate, differential reinforcement of low rate in Experiment 2). Rats were then transferred to a multiple fixed interval (FI; 60-sec, 60-sec) schedule, until the effects of the first phase on response rate were no longer apparent and their response rates did not differ from those of rats responding on a multiple FI 60-sec, FI 60-sec schedule without previously experiencing a multiple RR, RI schedule. During the third stage oftraining, all rats were placed into extinction. During extinction, rates of responding were higher in the component previously associated with the high rate of responding in Phase 1, and they were lower in the component previously associated with low rates of responding in Phase 1. These results suggest that resurgence effects, like other history effects, are controlled by previous rates of responding. 相似文献
19.
Resurgence is the recurrence of a previously reinforced and then extinguished behavior induced by the extinction of another more recently reinforced behavior. Resurgence provides insight into behavioral processes relevant to treatment relapse of a range of problem behaviors. Resurgence is typically studied across three phases: (1) reinforcement of a target response, (2) extinction of the target and concurrent reinforcement of an alternative response, and (3) extinction of the alternative response, resulting in the recurrence of target responding. Because each phase typically occurs successively and spans multiple sessions, extended time frames separate the training and resurgence of target responding. This study assessed resurgence more dynamically and throughout ongoing training in 6 pigeons. Baseline entailed 50-s trials of a free-operant psychophysical procedure, resembling Phases 1 and 2 of typical resurgence procedures. During the first 25 s, we reinforced target (left-key) responding but not alternative (right-key) responding; contingencies reversed during the second 25 s. Target and alternative responding followed the baseline reinforcement contingencies, with alternative responding replacing target responding across the 50 s. We observed resurgence of target responding during signaled and unsignaled probes that extended trial durations an additional 100 s in extinction. Furthermore, resurgence was greater and/or sooner when probes were signaled, suggesting an important role of discriminating transitions to extinction in resurgence. The data were well described by an extension of a stimulus-control model of discrimination that assumes resurgence is the result of generalization of obtained reinforcers across space and time. Therefore, the present findings introduce novel methods and quantitative analyses for assessing behavioral processes underlying resurgence. 相似文献
20.
Schedules of reinforcement typically produce reliable patterns of behaviour, and one factor that can cause deviations from these normally reliable patterns is schizotypy. Low scorers on the unusual experiences subscale of the Oxford-Liverpool Inventory of Feelings and Experiences performed as expected on a yoked random-ratio (RR), random-interval (RI) schedule of reinforcement, with significantly higher rates of responding on the RR schedule than in the RI schedule. However, high scorers in UE showed no such differences between response rates between the RR and RI schedules. In addition, contingency awareness scores were high, and did not differ in low UE scorers for both types of schedule, whilst awareness scores differed significantly between the schedules in high UE scorers, with more awareness of the RR schedule than the RI one. These results suggest that, as well as being unable to differentiate between the RR and RI schedules in terms of response rates, high UE scorers are also unable to verbally describe the RI schedule parameters. 相似文献