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1.
Two experiments were conducted to investigate functional similarities between “hunger CRs” of Konorski’s (1967) model of appetitive classical conditioning and sign-tracking behavior in rats. Konorski’s model predicts that hunger CRs will be facilitated (1) when a nonrein-forced stimulus similar to the reinforced CS is introduced, and (2) when some CS presentations are unexpectedly nonreinforced. In Experiment 1, hungry rats acquired a leverpress response to a retractable lever that was paired with response-independent food. Following this training, a second lever was introduced whose presentation was not followed by food. The effect of the presence of this second lever was to facilitate responding to the original lever. In Experiment 2, single-lever autoshaping training was followed by a shift from 100% pairing of the lever with food to only 50% of the lever presentations being followed by food. The introduction of partial reinforcement produced an immediate and durable increase in leverpressing. The findings of both experiments are consistent with predictions from Konorski’s model of classical conditioning if sign-tracking is considered as a “hunger CR.”  相似文献   

2.
Sated rats, previously trained to leverpress for H2O reinforcement on continuous or variable-interval (10-sec or 60-sec) schedules, were given NaCl injections and tested for leverpressing. Under all schedules, responding was an inverted U function of NaCl concentration (0.15M to 3.0M). However, NaCl thirst produced relatively little change in behavior under the VI 60-sec schedule.  相似文献   

3.
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   

4.
The conservation model was generalized to the variable-interval schedule by incorporating the concept of unscheduled instrumental responses, those which occur in the time before the next setup is due. Thirsty rats responded in constant-duration sessions on two 7-sec schedules that required one leverpress for 25 and 50 licks at a water tube and on a 14-sec 25-lick schedule. In accordance with the model, total licks decreased linearly as total presses increased, and the schedules facilitated leverpressing and suppressed licking relative to paired baseline levels of responding. While the matching model also gave a satisfactory fit to instrumental responding under the schedules, its two constants, representing asymptotic rate of responding and extraneous reinforcement, had anomalous values which led the model to predict that response rate would decrease as the rate of reinforcement increased, directly opposing its prediction for the constant-consumption experiments of its previous tests.  相似文献   

5.
Suppression of operant responding during a conditioned stimulus (CS) was studied in two procedures. In both procedures, operant leverpressing was maintained by a variable-interval 1-min food-delivery schedule, and insertion of a second lever served as the CS. In the first procedure, autoshaping, food followed each CS presentation irrespective of a subject’s behavior during the CS. In the second procedure, omission training, contact with the CS canceled the delivery of food scheduled for the end of that CS. In the first experiment, subjects were exposed to omission training followed by autoshaping; these procedures were reversed in the second experiment. In each experiment, the omission contingency resulted in fewer CS contacts and less suppression of operant responding during the CS than did autoshaping. These differences were more notable in subjects receiving the sequence autoshaping→omission training (Experiment 2). Direct observations in Experiment 2 revealed that, for subjects that were contacting the CS frequently when the omission contingency was introduced, reductions in signal contacts were accompanied by redistributions of behavior. The form of these redistributions depended upon behavior allocation at the time the omission contingency was imposed.  相似文献   

6.
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.
Conditioning-specific reflex modification (CRM) of the rabbit’s nictitating membrane response (NMR) describes changes in responding to an unconditioned stimulus (US) when the rabbit is tested in the absence of the conditioned stimulus. Specifically, after at least 3 days of tone-electrical stimulation pairings, responses to the US increase in size, especially at intensities weaker than the training intensity. CRM is similar to classical conditioning in that it is a function of the strength of conditioning, it can be extinguished, and it can be generalized from one stimulus to another. To compare CRM and classical conditioning further, we conducted three experiments to examine the effects of US intensity (1.0, 2.0, and 4.0 mA) on CRM. CRM was weak following conditioning with 1.0 mA and extremely strong following conditioning with 2.0 mA and 4.0 mA. The data suggest that CRM is a function of US intensity and have implications for posttraumatic stress disorder, a disorder potentially modeled by CRM.  相似文献   

8.
The experiments reported in the present study tested whether decreasing intertrial intervals (ITIs) intensifies the disruptive effects of increasing retention intervals (RIs) in a delayed conditional discrimination by decreasing the animal’s trial tracking accuracy (Cohen & Armstrong, 1996; Cohen & Roberts, 1996). Rats responded on a fixed ratio (FR) 1 or fixed interval (FI) 10-sec reinforcement schedule at a second light or tone stimulus, S2, when the first light or tone stimulus, S1, had signaled an FI 10-sec or FR 1 schedule, respectively. RIs between S1 and S2 were increased from 3 to 24 sec and never exceeded ITIs that were reduced from 24 to 6 sec. For some rats, the trials were separated from each other by extending the lever at S1 and retracting it at the end of S2 (ITI lever-retracted group). For other, control rats, the lever remained extended throughout the session (lever-extended group, Experiment 1) or was extended and retracted with the onset and offset of each stimulus (RI/ITI lever-retracted group, Experiment 2). The rats under all trial conditions learned to delay leverpressing on the FI 10-sec schedule. Latency to begin leverpressing on the FI 10-sec schedule declined as RIs were increased, but this effect was attenuated in the ITI lever-retracted groups in both experiments, as would be predicted by thetrial tracking hypothesis. Decreasing ITIs from 24 to 6 sec intensified the disruptive effects of increasing RIs from 3 to 6 sec in the RI/ITI lever-retracted group (Experiment 2), as would be predicted by the trial tracking hypothesis.  相似文献   

9.
Two experiments tested the hypothesis that habituation contributes to within-session decreases in responding. In Experiment 1, rats’ leverpressing was reinforced under a fixed ratio (FR) 4 schedule throughout the baseline sessions. During the dishabituation sessions, the first 21 min and the last 21 min were FR 4; dishabituating events occurred during the middle 3 min. The dishabituating events altered the manner of reinforcer delivery in four different ways. Response rates increased after all dishabituating events. In Experiment 2, rats responded on several FR and variable ratio (VR) schedules. The ratio requirement varied from 3 to 15. Within-session decreases in responding were steeper during FR schedules than during VR schedules. In addition, response rates were well described as linear functions of cumulative number of food pellets eaten within sessions. These results support the habituation hypothesis but do not rule out the possibility that other satiety variables might contribute simultaneously.  相似文献   

10.
In two experiments, the possibility of outcome-selective reinstatement of conditioned responding was examined. Evidence for outcome-selective reinstatement of previously extinguished appetitively conditioned magazine responses by rats was observed in both Pavlovian (Experiment 1) and discriminated instrumental conditioning (Experiment 2) procedures. In both experiments, stimulus-elicited magazine responses occurred more in the presence of a stimulus whose reinforcer was reinstated than they did in the presence of another stimulus whose reinforcer was not reinstated. This effect was observed after both brief and extensive amounts of extinction. Outcome-selective reinstatement of instrumental leverpressing, however, was not observed, although nonselective reinstatement of magazine responding and leverpressing was obtained in Experiment 2. Overall, the data from these studies challenge existing theories of reinstatement, and they provide additional evidence of the importance of outcome-specific processes in the control of learned performance.  相似文献   

11.
In Experiment 1, male rats were trained to press both bars in a two-choice apparatus and were then given observational training of a go/no-go discrimination in which the observed operation of two inaccessible, dissimilar bars by a hidden experimenter constituted S+ and S?. After discrimination was established, individual rats were permitted access to the two bars. Six of the seven rats consistently pressed the S+ bar on 10 test trials, but failed to reverse bar preference after observational training was reversed. In Experiment 2, nine naive males received the same observational training as in Experiment 1, but without any pretraining to press either bar. All rats pressed the S+ bar on initial test and did so consistently throughout the 10 trials. Six of these rats received reversal training of the go/no-go discrimination after the 10 test trials. As in Experiment 1, all rats failed to press the new S+ bar. However, five of six rats in another group, which received reversal trainingprior to any test trials, did reverse and press the new S+ bar. In Experiment 3, controls for possible confounding effects of overtraining trials were conducted. These manipulations had no effect; the rats tested before reversal still failed to press the S+ bar, and the rats reversed before testing all reversed or pressed the most recent S+ bar. That is, S-R learning predominated over S-S learning if active, though unreinforced, responding to a particular bar intervened. In contrast, however, a cognitive (S-S) interpretation of directed response learning was supported by the results of Experiment 4, in which the rats that learned the go/no-go discrimination without responding (only by auditory and light cues) failed to press the S+ bar consistently.  相似文献   

12.
In Experiment 1, three groups of rats received a tactile prepulse 0.5, 1, or 2 mA electric shock (to feet) .25, .5, 1, 5, 10, or 20 sec prior to an acoustic startle stimulus. The startle response was, maximally inhibited at the .25-sec interval and gradually recovered thereafter. Inhibition was larger with the intense stimuli, and for the .5-mA stimulus occurred reliably only in animals which responded to the prestimulus. In Experiment 2, the intensity of the prepulse was varied within subjects at intervals of .5, 1, and 2 sec. Inhibition was directly related to prestimulus intensity and was greatest at .5 sec. In Experiment 3, an EMG measure of startle reactivity allowed the use of shorter intervals. The maximal inhibitory interval between the prestimulus and startle stimulus was 40 msec compared with either a shorter 10-msec or a longer 250-msec separation.  相似文献   

13.
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   

14.
In four experiments, we examined how the spatiotemporal proximity to food of the two elements of a serial conditioned stimulus (CS) influenced the pattern of CS-directed versus food-site-directed behavior in rats. Experiment 1 showed that only temporal proximity affected responding when the serial CS consisted of two successive 4-sec presentations of either a spatially near or a spatially far lever (NN or FF). However, Experiment 2 showed that behavior depended markedly on whether rats received a near followed by a far lever (NF) or a far followed by a near lever (FN). Experiment 3 showed that the effects of Experiment 2 could be changed by increasing the duration of the second CS element, and Experiment 4 showed that these changes were not related to previous training. We concluded that behavior produced by the spatiotemporal qualities of the lever elements can be attributed to a mapping between the temporal qualities of the CS elements and an underlying sequence of search modes related to finding food.  相似文献   

15.
In Experiment 1, rats were trained to leverpress on a variable ratio (VR) 30 schedule with a 500-msec delay between the reinforced response and food delivery. Subjects that experienced a signal during the delay responded faster than did control subjects that received the stimulus un-correlated with reinforcement. Higher response rates were obtained when the stimulus used to signal reinforcement was auditory rather than visual. Experiments 2 and 3 compared the effects of signaling reinforcement with either a localized or a diffuse light on responding maintained by VR schedules of reinforcement. Elevated response rates were observed with the diffuse stimulus, but the localized stimulus failed to produce such potentiation. Experiment 3 also examined the conditioned reinforcing power of localized and diffuse visual stimuli. These results are discussed with reference to (1) theories of selective association and sign tracking and (2) their implications for current theories of signaling reinforcement.  相似文献   

16.
Latency measures of starting to drink and of consummatory behavior were used to investigate ingestional neophobia to novel visual and novel taste cues in chicks. In Experiment 1 (N = 36), latencies to start drinking were reliably shorter to ingesta that appeared familiar from previous rearing or preexposure procedures. After drinking started, consummatory responding occurred reliably more rapidly to familiar taste cues than to novel ones. However, the presence of familiar visual cues reliably facilitated consumption of a novel taste. Experiments 2 and 3 (Ns = 144 and 180) were performed to evaluate, respectively, whether the ingestional effects of taste stimulus intensity, 0%–6% vinegar, and of visual stimulus intensity, 0%–1.0% concentrations of red food-coloring in water, changed during ontogeny for chicks 3, 5, and 7 days old. In Experiment 2, reliable direct effects of taste concentration on consummatory response latencies occurred immediately in 7-day-olds but were delayed in 3-day-olds. In Experiment 3, each age group immediately showed reliably slower starting and consummatory response times, the higher the concentration of red food-coloring. Intake performance in both experiments was consistent with the latency data. Experiments 1–3 showed that visual and taste cues of ingesta separately influenced approach and consummatory behaviors of the ingestive response sequence and that these influences depend on ontogenetic events.  相似文献   

17.
Pigeons pecked keys on concurrent-chains schedules that provided a variable interval 30-sec schedule in the initial link. One terminal link provided reinforcers in a fixed manner; the other provided reinforcers in a variable manner with the same arithmetic mean as the fixed alternative. In Experiment 1, the terminal links provided fixed and variable interval schedules. In Experiment 2, the terminal links provided reinforcers after a fixed or a variable delay following the response that produced them. In Experiment 3, the terminal links provided reinforcers that were fixed or variable in size. Rate of reinforcement was varied by changing the scheduled interreinforcer interval in the terminal link from 5 to 225 sec. The subjects usually preferred the variable option in Experiments 1 and 2 but differed in preference in Experiment 3. The preference for variability was usually stronger for lower (longer terminal links) than for higher (shorter terminal links) rates of reinforcement. Preference did not change systematically with time in the session. Some aspects of these results are inconsistent with explanations for the preference for variability in terms of scaling factors, scalar expectancy theory, risk-sensitive models of optimal foraging theory, and habituation to the reinforcer. Initial-link response rates also changed within sessions when the schedules provided high, but not low, rates of reinforcement. Within-session changes in responding were similar for the two initial links. These similarities imply that habituation to the reinforcer is represented differently in theories of choice than are other variables related to reinforcement.  相似文献   

18.
19.
After rats had been trained to press a lever for food reward, experimenter-initiated food “primes” increased the likelihood of subsequent responding during periods in which the subjects were nondeprived. No such priming effects were found after presentation of a stimulus that had previously been paired with food. In other experiments, nonreinforced leverpresses, as well as subthreshold components of the leverpress response (e.g., forepaw raising), were also found to be enhanced by food primes. Taken together with other reports in the literature, the present findings are consistent with a “motivational aftereffects” interpretation of priming, and also with the notion that all stimuli which possess reinforcing properties possess priming properties as well.  相似文献   

20.
In four experiments with rats, we examined the persistence of behavior when reinforcement was switched from immediate to delayed. In Experiment 1, lever pressing elicited by instrumental training with immediate reinforcement continued when a 20-sec delay of reinforcement was introduced (easy-to-hard condition), whereas when the delay condition was introduced from the start (hard-to-hard condition), responding remained low throughout. A similar result was obtained in Experiment 2, in which lever pressing was elicited by a classical conditioning (autoshaping) procedure. In Experiment 3, rats initially trained with delayed reinforcement continued to respond at a low rate when switched to immediate reinforcement (hard-to-easy condition). By measuring magazine entry (goal tracking) as well as lever pressing (sign tracking) in Experiment 4, we confirmed that such transfer effects at least partly involve the persistence of whatever type of behavior was initially dominant.  相似文献   

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