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1.
In previous studies of anticipatory contrast, identical target components (A and B) preceded either a lower (extinction) or a richer schedule. Higher response rates occurred during the target preceding the lower rate of reinforcement, whereas preference was in favor of the target preceding the richer schedule. In Experiment 1, the response and preference measures were positively related when additional stimuli, with no reinforcement of their own, preceded the target components. The effect of these additional stimuli was presumed to be due to their overshadowing of the Pavlovian association between the target components and their following schedules. Experiment 2 also demonstrated a consistent relation between response rate and preference in a conditioned reinforcement procedure. In the absence of a strong Pavlovian association, anticipatory contrast, like other forms of contrast in free-operant procedures, reflects an increase in the value of the target component with an unchanged reinforcement schedule. 相似文献
2.
We present an algebraic model of resistance to extinction that is consistent with research on resistance to change. The model assumes that response strength is a power function of reinforcer rate and that extinction involves two additive, decremental processes: (1) the termination of the reinforcement contingency and (2) generalization decrement resulting from reinforcer omission. The model was supported by three experiments. In Experiment 1, 4 pigeons were trained on two-component multiple variable-interval (VI) 60-sec, VI 240-sec schedules. In two conditions, resistance to change was tested by terminating the response-reinforcer contingency and presenting response-independent reinforcers at the same rate as in training. In two further conditions, resistance to change was tested by prefeeding and by extinction. In Experiment 2, 6 pigeons were trained on two-component multiple VI 150-sec schedules with 8-sec or 2-sec reinforcers, and resistance to change was tested by terminating the response-reinforcer contingency in three conditions. In two of those conditions, brief delays were interposed between responses and response-independent reinforcers. In both Experiments 1 and 2, response rate was more resistant to change in the richer component, except for extinction in Experiment 1. In Experiment 3, 8 pigeons were trained on multiple VI 30-sec, VI 120-sec schedules. During extinction, half of the presentations of each component were accompanied by a novel stimulus to produce generalization decrement. The extinction data of Experiments 1 and 3 were well described by our model. The value of the exponent relating response strength and reinforcement was similar in all three experiments. 相似文献
3.
Pigeons served in two experiments in which responding on an observing key converted a two-component mixed schedule to the corresponding multiple schedule of reinforcement. Presentation of the stimulus correlated with the more valued component was faded out (probabilistically) over sessions, so that ultimately an observing response produced only the stimulus correlated with the less valued component. Observing was well maintained after a fading procedure when a stimulus was produced by a single response, regardless of whether the less valued stimulus was associated with food or with extinction (Experiment 1). However, observing was not well maintained after a fading procedure when a stimulus was produced according to an intermittent schedule (Experiment 2). Taken together, the results of the two experiments suggest that the absence of an exteroceptive stimulus change after a single response may become discriminative in its own right for the more valued component, and that the fading procedure is an effective means of promoting this discrimination. However, if observing responses produce a stimulus change according to an intermittent schedule, then the absence of a stimulus change after a response is correlated with both components. Under these conditions, the absence of stimulus change is not discriminative for either component, even with fading, and observing is not maintained. 相似文献
4.
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
5.
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
6.
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
7.
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
8.
Ben A. Williams 《Learning & behavior》1988,16(2):206-216
Pigeons were trained on multiple schedules with component stimuli of different degrees of similarity. In Experiment 1, a two-component schedule was used in which the two stimuli were either two line orientations or a line orientation versus a diffuse color. Reinforcement rate was varied in one component to determine the effects of stimulus similarity on different aspects of behavioral contrast. Contrast in terms of average response rates (molar contrast) was larger with less similar stimuli. Local contrast effects at the beginning of the component were larger for more similar stimuli, but these effects were more variable and did not attain statistical significance. Independent of the level of molar contrast, the local pattern of schedule interaction differed for the two levels of similarity: with more similar stimuli, the maximum degree of interaction occurred at the beginning of the components and then decreased; with less similar stimuli, the degree of interaction increased throughout the components and was at its maximum near their end. In Experiment 2, the same three stimuli were used while reinforcement rate in the middle component of a three-component sequence was varied; this isolated the effects of the preceding schedule from those of the following schedule. Contrast effects were generally greater in the target component preceding the variable schedule, and these were enhanced by less similar stimuli. Contrast in the target component following the variable schedule was manifested primarily in terms of the behavior at the beginning of the component, and these effects were inconsistently related to stimulus similarity. The functional separation of the effects of stimulus similarity on the different locations of contrast suggest that “anticipatory contrast” and “local contrast” depend upon different mechanisms, thus excluding any account of contrast solely in terms of relative rate of reinforcement. 相似文献
9.
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
10.
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
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13.
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
14.
In the present experiments, we investigated the effects of mindfulness on behavioral extinction and resurgence. Participants received instrumental training; either they received FI training (Experiment 1), or they were trained to emit high rates and low rates of response via exposure to a multiple VR yoked-VI schedule prior to exposure to a multiple FI FI schedule in order to alter their rates of responding learned during Experiment 2. Participants were then exposed to either a focused- (mindfulness) or an unfocused-attention induction task. All participants were finally exposed to an extinction schedule in order to determine whether a mindfulness induction task presented immediately prior to extinction training affected extinction (Experiment 1) and behavioral resurgence (Experiment 2). During the extinction phase, the rates of responding were higher in the control group than in the mindfulness group, indicating that the mindfulness group was more sensitive to the contingencies and, thus, their prior performance extinguished more readily (Experiment 1). Moreover, rates of response in the extinction components less precisely reflected previous training in the mindfulness group, suggesting less resurgence of past behaviors after the mindfulness induction (Experiment 2). 相似文献
15.
Behavior reduced as a consequence of extinction or intervention can relapse. According to behavioral momentum theory, the extent to which behavior persists and relapses once it has been eliminated depends on the relative training reinforcement rate among discriminative stimuli. In addition, studies of context renewal reveal that relapse depends on the similarity between the training stimulus context and the test stimulus context following disruption by extinction. In the present experiments with pigeons, we arranged different reinforcement rates in the presence of distinct discriminative stimuli across components of a multiple schedule. Following extinction, we attempted to reinstate responding in the presence of those target components with response-independent food presentations. Importantly, we arranged the reinstating food presentations either within the target components or in separate components, either paired with extinction (Experiment 1) or reinforcement (Experiment 2) during baseline. Reinstatement increased with greater training reinforcement rates when the reinstating food presentations were arranged in the target components and the separate components paired with reinforcement during training. Reinstatement was smaller and was not systematically related to training reinforcement rates in the target components when reinstating food presentation occurred in separate components paired with extinction. These findings suggest that relapse depends on the history of reinforcement associated with the discriminative stimuli in which the relapse-inducing event occurs. 相似文献
16.
Five rats responded on several concurrent schedules in which pressing a key produced reinforcers in one component and pressing a lever produced reinforcers in the other component (Experiment 1). Four pigeons responded on several concurrent keypeck treadlepress schedules (Experiment 2). The programmed rates of reinforcement varied from 15 to 240 reinforcers per hour in different conditions. Rates of responding usually changed systematically within experimental sessions, and the changes were similar for the two components of a concurrent schedule. These results imply that within-session changes in responding may not confound the predictions of theories that describe the ratio of the rates of responding during the two components of concurrent schedules. Instead, within-session changes may be controlled by a mechanism that integrates the reinforcers obtained from the two components. 相似文献
17.
Experiment 1 investigated the behavior of rats trained to leverpress on a concurrent variable ratio (VR) 30 VR-30 schedule with a brief, 500-msec, light occurring at the midpoint of the ratio on one of the levers. Higher response rates were recorded on the lever associated with this stimulus, a finding that paralleled the effect produced by inserting primary reinforcement at the midpoint (i.e., by training on a concurrent VR-30 VR-15 schedule). Similar results were found in Experiment 2 using a concurrent VR-20 VR-20 schedule with a 2-sec visual stimulus presented midway through one of the components. In addition, a brief stimulus inserted midway through the VR-20 component of a concurrent VR-20 VR-10 schedule retarded the development of a difference in response rates between the components relative to a VR-20 VR-10 group lacking the signal. In Experiment 3, multiple VR VR schedules were used. Again, the response rate was higher in the component that had the added stimulus or, for a second group of subjects, on the component with the smaller response requirement. Probe-choice trials revealed a preference for the component that generated the higher rate in both groups. Presenting a stimulus partway through a ratio appears to reduce the effect on response rate and choice of a large ratio value. 相似文献
18.
William P. Bellingham Katy Gillette-Bellingham E. James Kehoe 《Learning & behavior》1985,13(2):152-164
Discrimination between a tone + light compound and its components in positive and negative patterning schedules was examined. In the positive schedule, reinforced compound presentations (C+) were intermixed with unreinforced component presentations (T?, L?). In the negative schedule, the compound was unreinforced (C?) and the components were reinforced (T+, L+). In Experiment 1, appetitive conditioning of rats’ anticipatory magazine responses was used, and in Experiment 2, aversive conditioning of the rabbit’s nictitating membrane response was used. Both experiments revealed that the positive patterning schedule consistently produced rapid acquisition of appropriate discriminative responding. The results of the negative patterning schedule were more complex. Specifically, the results of Experiment 1 demonstrated that naive rats initially showed rapid acquisition of the negative patterning discrimination. However, schedule reversals revealed that experience with the positive patterning schedule virtually abolished subsequent acquisition of discriminative responding under the negative patterning schedule. The results of Experiment 2 revealed that naive rabbits showed very slow acquisition of discriminative responding under the negative patterning schedule. The results are discussed in relation to the unique-stimulus hypothesis, a contextual encoding hypothesis, and a configural hypothesis. 相似文献
19.
Two accounts of how density of reinforcement affects steady-state performance on probabilistic schedules were compared: the real-time linear operator (RTLO) model and a temporal control model (in which response strength is determined by reinforcement probability as a function of postreinforcement time). In Experiment 1, the probability of reinforcement repeatedly cycled between extinction and a random-ratio 10 schedule. Response-rate gain and phase did not change with period of the cycle as predicted by the RTLO model, nor did either model predict the differences in response rate following reinforcement at different points in the cycle. In Experiment 2, the probability of reinforcement was elevated immediately following a reinforcement but fell after a few seconds. Previous reinforcements had no effect upon responding. An extension of the temporal control model, the cumulative impulse model, allowed for the summing of response strength over successive reinforcements and was consistent with the data of both experiments. 相似文献
20.
In three experiments, we examined the effect on the patterns of responding noted on fixed interval (FI) schedules of prior
exposure to a range of interval and ratio schedules. Rats leverpressed for food reinforcement on random ratio (RR), random
interval (RI), or variable interval (VI) schedules prior to transfer to FI schedules. In Experiment 1, prior exposure to an
RR schedule retarded the development of typical FI patterns of responding. Exposure to a yoked RI schedule produced even greater
retardation of typical FI performance. This effect was replicated in Experiment 2, using a within-subjects design. Rats responded
on a multiple RR-RI schedule prior to a multiple FI-FI schedule. Typical FI performance emerged more slowly in the component
previously associated with the RI than with that associated with the RR. In Experiment 3, exposure to an RR schedule retarded
the development of FI performance to a greater extent than did exposure to a VR schedule. The latter schedule was programmed
to allow the possibility that inhibitory control would develop after reinforcement. These results confirm that ratio schedules
independently result in the disruption of FI responding. This effect was not long lasting and cannot be used plausibly to
explain species differences in responding to FI schedules. However, it does suggest that temporal control—as manifested by
the transfer of inhibitory control from one schedule to another—could facilitate movement between interval schedules. 相似文献