共查询到20条相似文献，搜索用时 15 毫秒
1.
John H. Hull 《Learning & behavior》1977,5(2):207-212
Experiments 1, 2, and 3 showed that food-deprived rats responding for food pellets made significantly more long-duration leverpresses than water-deprived rats responding for water drops. These experiments further showed that this difference in instrumental response topography is long-lived, and depends neither upon idiosyncrasies of the experimental chamber nor upon severity of deprivation conditions. In Experiment 4, food-deprived rats responding for food pellets made significantly more long-duration leverpresses than did either food- or water-deprived rats responding for sucrose solution. Human judges in Experiment 5 were able to correctly identify instrumental leverpress responses by rats as being for food or water based solely on previous viewings of other rats drinking water or eating food pellets. It appears that instrumental response topographies in rats vary depending principally upon the reinforcer received, and that these instrumental response topographies resemble consummatory response topographies. 相似文献
2.
Peter C. Holland 《Learning & behavior》2014,42(4):365-382
Initially neutral conditioned stimuli paired with food often acquire motivating properties, including serving as secondary reinforcers, enhancing instrumental responding in Pavlovian-instrumental transfer procedures, and potentiating food consumption under conditions of food satiation. Interestingly, cues associated with the cancellation of food and food cues may also potentiate food consumption (e.g., Galarce and Holland, 2009), despite their apparent negative correlations with food delivery. In three experiments with rats, we investigated conditions under which potentiation of feeding by such “interruption stimuIi” (ISs) develops, and some aspects of the content of that learning. Although in all three experiments ISs enhanced food consumption beyond control levels, they were found to act as conditioned inhibitors for anticipatory food cup entry (Experiment 1), to serve as conditioned punishers of instrumental responding (Experiment 2), and to suppress instrumental lever press responding in a Pavlovian instrumental transfer procedure (Experiment 3). Furthermore, when given concurrent choice between different foods, an IS enhanced consumption of the food whose interruption it had previously signaled, but when given a choice between performing two instrumental responses, the IS shifted rats’ choice away from the response that had previously yielded the food whose interruption had been signaled by IS (Experiment 3). Thus, the effects of an IS on appetitive responses were opposite to its effects on consummatory responding. Implications for our understanding of learned incentive motivation and the control of overeating are discussed. 相似文献
3.
Four experiments examined the influence of a stimulus presented after one response in a two-lever choice task. In Experiment 1, food-deprived rats trained on a concurrent variable-interval extinction schedule responded more often on the extinction lever when such responding periodically produced a visual stimulus than when it did not. In Experiments 2 and 3, a similar signal-induced enhancement effect was found even when food was delivered randomly with respect to responding on both levers or when no food was presented. In Experiment 4, a response-contingent visual stimulus elevated responding to the lever on which it was presented, but an auditory cue suppressed responding. These findings indicate that visual stimuli may possess intrinsically reinforcing properties for rats. 相似文献
4.
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
5.
In three experiments the sensitivity of instrumental responding to revaluation of the instrumental outcome in the absence of experience with the revalued outcome was examined. Hungry rats were trained to make one response for food pellets and a different response for sucrose liquid. In Experiment 1, these responses were tested in extinction when the animals were either thirsty or hungry. A significant preference for the sucrose-trained response was observed in the test conducted under thirst but not in that conducted under hunger. In Experiments 2 and 3, the effect of experience with sucrose under thirst on the magnitude of this preference was explored. Following training of the instrumental responses in Experiment 2, half of the animals received presentations of sucrose while they were thirsty; the other half received sucrose while they were hungry. In Experiment 3, the same design was used but these sucrose presentations were made contingent on an instrumental response. Also in Experiment 3, the specificity of the sucrose-response preference to a shift to thirst was examined by testing under increased and decreased levels of hunger. The results of those experiments indicated that the sucrose-response preference is exhibited only under thirst and that exposure to the sucrose under thirst only marginally enhanced that preference. These findings suggest that instrumental responding may be modified by changes in the value of its outcome in the absence of experience with the revalued outcome. 相似文献
6.
A. G. Baker 《Learning & behavior》1990,18(1):59-70
Three experiments were designed to study the effects of contextual conditioning on the extinction of instrumental leverpressing that had been reinforced on a random-interval schedule. In Experiment 1, noncontingent food retarded extinction, but signaling food delivery, a treatment that should reduce contextual conditioning, reduced the interference. Experiment 2 replicated the results of Experiment 1 and demonstrated that if the food preceded rather than followed the signal, the retardation of extinction was not reduced but was enhanced. In Experiment 3, non-contingent leverpressing was used to directly verify that the three treatments—forward signaling, noncontingent food, and backward signaling—differentially influenced contextual conditioning. Forward signaling produced the least, and backward signaling produced the most, contextual conditioning. This monotonic relationship between contextual conditioning and interference with extinction was used as evidence to support the argument that context-food associations are important in controlling instrumental responding. 相似文献
7.
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
8.
In three experiments that used appetitive preparations with rats, we examined the effects of reinforcing a compound consisting of two previously reinforced stimuli on subsequent responding to those stimuli. Experiment 1 showed that a Pavlovian conditioned stimulus given this treatment evoked fewer magazine entries when presented alone than did a reinforced stimulus that did not receive the compound treatment. Experiment 2 examined inhibition of delay and generalization decrement accounts for the results of Experiment 1. Experiment 3 extended this finding to an instrumental learning paradigm. 相似文献
9.
10.
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
11.
Four experiments examined the effects of separate presentations of shock on conditioned suppression of instrumental responding evoked by a CS previously paired with shock. Experiment 1 showed that conditioned suppression of responding resulting from noise-shock pairings increased as a function of time after the initial noise-shock pairings. However, it also showed that this time-dependent increase in conditioned suppression of responding could be attenuated by presentations of light-shock pairings immediately prior to the test of the noise CS. Experiment 2 showed that this attenuation effect can be produced by presentations of either light-shock pairings or shock alone. Experiment 3 showed that the magnitude of this attenuation effect was directly related to the temporal proximity of the light-shock pairings to the test of the noise CS. Experiment 4 showed that the magnitude of this attenuation effect was inversely related to the intensity of separate shock presentations. 相似文献
12.
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
13.
Previous research has demonstrated that running in a rotating wheel functions as a reinforcer for leverpressing in rats. In these studies, the pattern of responding was similar to the pattern of responding maintained by consummatory reinforcers, such as food and water. The present study investigated quantitative features of responding maintained by running. In previous experiments in which responses were reinforced according to variable-interval (VI) schedules and food and water served as the reinforcer, the equation for a rectangular hyperbola described the relationship between response rate and reinforcement rate. This experiment tested whether this quantitative regularity also applies to leverpressing maintained by the opportunity to run in a wheel. Fourteen male Wistar rats responded on levers for the opportunity to run. In each session, subjects were exposed to a series of VI schedules. An opportunity to run for 60 sec was the reinforcing consequence. Results showed that response rate was a negatively accelerated function of reinforcement rate, and the relationship between these two variables was described well by the equation for a rectangular hyperbola. To further test the similarity between running and consummatory reinforcers, the response requirement and access were manipulated. In previous experiments with food and water, these types of manipulations differentially changed the two parameters of the hyperbola. A similar pattern of results was obtained with wheel running. Thus, the equation appears to apply to running about as well as it does to consummatory reinforcers. 相似文献
14.
Ken Cheng 《Learning & behavior》1992,20(2):112-120
The peak procedure was used in two experiments. Pigeons in the penalty group in Experiment 1 were rewarded with food in the first phase for the first peck after 12.5 sec had elapsed since the onset of a keylight. In the second phase, reward was withheld if the pigeons pecked within 6.25 sec after keylight onset. Responses in time were tabulated on occasional unrewarded tests in which the keylight was left on for 37.5 sec. Under the penalty contingencies, the response distribution in time remained nearly symmetric about the peak, while the spread of the distribution narrowed, and the time of peak responding came slightly earlier. The yoke group underwent a schedule of rewards similar to that for the penalty group, but without the penalty contingencies. Their response distributions remained similar throughout. The results of Experiment 1 were replicated in Experiment 2, which showed further that the changes due to the penalty contingencies did not generalize to the use of another key on which the penalty contingencies were not in effect. The narrower spread under the penalty contingencies is explained in terms of a change in threshold for when to start responding, and more weight being given to timing versus responding in the presence of the signal per se. No explanation was found for the change in the time of peak responding. 相似文献
15.
In four experiments utilizing an appetitive conditioning preparation, reacquisition of conditioned responding was found to occur both rapidly and slowly following extinction. In Experiment 1, acquisition of responding to a tone that had been conditioned and extinguished occurred more rapidly than acquisition in either a group that received equivalent exposure to the food unconditioned stimulus or a “rest” control group that received only exposure to the apparatus in the first two phases. However, reacquisition was impaired relative to acquisition in a “learning-experienced” group that had previously received conditioning and extinction with a different stimulus. Experiments 2 and 3 produced similar results, but also found that high responding during reacquisition was confined to trials that followed reinforced, rather than nonreinforced, trials. Experiment 4, in which very few initial conditioning trials were used, produced reacquisition that was slow compared with both learning-experienced and rest controls. The results are consistent with a role for sequential learning: Reacquisition is rapid when animals have learned that reinforced trials signal other reinforced trials. 相似文献
16.
Charles I. Brooks 《Learning & behavior》1975,3(1):67-72
In Experiment I, rats which had received six partially reinforced runway acquisition trials, with a reward magnitude of 60 sec access to wet mash on rewarded trials, showed less persistent responding over highly massed extinction trials than subjects which had received the same acquisition schedule but reward magnitudes of either 1 or 10 45-mg pellets. In Experiment II, rats which had received six partially reinforced placements into one compartment of a two-compartment box, with 60 sec access to mash on rewarded placements, jumped a hurdle faster to escape nonreward than subjects which had received the same reward schedule but 10 45-mg pellets on rewarded trials. The data supported a primary frustration analysis for reward-magnitude manipulations within brief partial-reinforcement schedules. 相似文献
17.
The effect of food deprivation level at the time of initial exposure to a subsequent food reinforcer was investigated in two experiments. In Experiment 1, deprivation at the time of initial exposure influenced the subsequent acquisition and extinction of an instrumental response. In Experiment 2, the residual deprivation effect associated with a reduction in deprivation level occurred only when rats initially experienced the reinforcer at a high, as compared with a low, deprivation level. Results were discussed in terms of the assumption that the limits of incentive generated by a reinforcer are influenced by the deprivation state at the time of first exposure to that reinforcer. 相似文献
18.
Three experiments with rat subjects examined the effects of contextual stimuli on performance in appetitive conditioning. A 10-sec tone conditioned stimulus (CS) was paired with a food-pellet unconditioned stimulus (US); conditioning was indexed by the observation of headjerking, a response of the rat to auditory stimuli associated with food. In Experiment 1, a context switch following initial conditioning did not affect conditioned responding to the tone; however, when the response was extinguished in the different context, a return to the original conditioning context “renewed” extinguished responding. These results were replicated in Experiments 2 and 3 after equating exposure to the two contexts (Experiment 2) and massing the conditioning and extinction trials (Experiment 3). The results of Experiment 1 also demonstrated that separate exposure to the US following extinction reinstates extinguished responding to the tone; this effect was further shown to depend at least partly on presenting the US in the context in which testing is to occur (Experiments 2 and 3). Overall, the results are consistent with previous data from aversive conditioning procedures. In either appetitive or aversive conditioning, the context may be especially important in affecting performance after extinction. 相似文献
19.
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
20.
Three experiments examine transfer from appetitive Pavlovian conditioning to appetitive instrumental responding by varying the similarity between conditions of Pavlovian reinforcement and instrumental reward. After conditioning with rats confined in a restraining device, a CS for electrical stimulation of the brain (ESB) produced substantial facilitation of operant responding for ESB, while a CS for food facilitated operant responding for food. However, no effects on rate of responding for food were seen during a CS for ESB. In a fourth experiment, four groups of rats were trained to barpress for rewarding electrical stimulation of the brain (ESB) and then given discriminative Pavlovian conditioning with ESB. The groups differed in the degree of similarity between the stimulus-response sequences present during Pavlovian conditioning and those occurring in instrumental responding. As similarity increased, so did the degree of conditioned facilitation in subsequent transfer tests. These results indicate that conditioned incentive responses or reinforcer-derived expectancies are specific to the conditions under which they develop, rather than generalized emotional or motivational responses. 相似文献