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1.
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
2.
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
3.
James Allison 《Learning & behavior》1980,8(2):185-192
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
4.
Six water-deprived pigeons were exposed to a fixed-time 90-sec water schedule with and without a conspecific target available. Target contacts and the pigeon’s location in the test chamber during the interreinforcement interval were recorded, and the results were compared with those previously obtained with food reinforcement. Prior to target introduction, water-reinforced birds spent more total time in the front near the reinforcer dispenser and less in the rear than food-reinforced birds and, unlike food-reinforced birds, exhibited postreinforcement drinking-like behaviors near the reinforcer dispenser before moving away from that area. With the target available, the level, topography, and duration of target-directed biting pecks were comparable for food- and water-reinforced pigeons. In contrast, the temporal organization of target pecks reflected the different temporal and spatial organizations of behavior prior to target introduction. For both food- and water-reinforced birds, the time between reinforcers at which a bird was spatially situated halfway between the front and rear of the chamber prior to target presentation was positively correlated with the time at which maximum target contact subsequently occurred. 相似文献
5.
In Experiment 1, rats were allowed to acquire either schedule-induced drinking or schedule-induced wood-chewing behavior under a fixed-interval (FI) 60-sec schedule of food reinforcement, following which food was omitted from 20% and then 50% of interreinforcement intervals. Omission of food severely disrupted induced drinking but had relatively little effect on induced wood-chewing. Experiment 2 investigated wood-chewing as a function of reinforcement rate, using a range of FI schedules from 5 to 180 sec in duration. Both the amount of chewing per session and the relative time spent chewing were bitonically related to reinforcement rate. In Experiment 3, schedule-induced chewing that had been acquired under a response-dependent schedule was found to persist under a response-independent schedule. Induced wood-chewing resembles other induced behaviors in important respects, but quantitative differences are also apparent. 相似文献
6.
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
7.
Three experiments were performed to investigate the preference of rats for either free or response-produced food. Rats were trained to free feed in an operant chamber and then to leverpress for food. Subsequently, they were given a choice between continuing to leverpress for food on CRF, FR 2, and FR 10 schedules or free feeding. In three experiments the independent variable was the method of free-food presentation: A fixed free-food dish was used in the first experiment, a movable dish in the second, and a large flat dish in the third experiment. The results of the three experiments were very similar, with most of the rats showing a preference for the free food. This preference increased further when more than one response was required to produce a food pellet. These results contradict any conclusion that rats have a generalized tendency to prefer response-produced to free food but provide no answer to the question of why rats do on occasion respond for food in the presence of free food. 相似文献
8.
A barpress analog to the double-alley runway was sought by varying percentage reward in the first of two consecutive FR 18s. Groups of six rats each were given 0% 50%. or 100% reinforcement upon completion of the first FR 18: after a 5-sec midtnal imterval, the second FR 18 was administered on a separate lever and all groups received CRF reward upon its completion. Group 50 Ss performed faster after nonreward than after reward. Group 50 Ss performed faster after nonreward than did 0% Ss. A measure of midtnal behavior revealed a difference between groups in orienting to the bars. When all groups were shifted to a 50% first component schedule (Phase II), there were no statistically reliable effects of prior reinforcement history on rewarded or nonrewarded responding. The Phase 1 results were taken to demonstrate a frustration effect similar to that of the double alley 相似文献
9.
Wild black-tailed prairie dogs were run on FR, FI, VR, and VI schedules for Noyes pellet reinforcement. Cumulative barpress responses, postreinforcement pause lengths, and responses per second were recorded. The highest response rates occurred in the VR schedules, with the lowest response rates coming in the FI schedules. Fixed-ratio schedules had the longest postreinforcement pauses, VI schedules had the shortest. At the upper levels of the fixed-ratio schedules (FR 90–100), the animals ceased to respond consistently. Generally, data from prairie dogs were consistent with data reported in studies from other mammalian species. 相似文献
10.
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
11.
Rats were trained to leverpress for food and subsequently exposed to either arithmetic series or random variable-interval reinforcement schedules. Adjunctive drinking developed in all subjects exposed to arithmetic variable-interval reinforcement, but did not develop in six of the eight animals trained on the random schedule. The results suggest that adjunctive drinking is the result of an interaction between the tendency of rats to drink after eating and the ability of locally low probabilities of reinforcement within schedules to induce conditioned behavioral states. 相似文献
12.
Rats subjected to FI 60-sec and FI 120-sec schedules of reinforcement were permitted concurrent access to a licking tube and a restrained target rat. While both polydipsia and attack occurred, polydipsia was the predominant scheduleinduced behavior. When attack occurred, and the licking tube was also available, attack usually followed licking in the interreinforcement interval. Eliminating access to the target did not influence polydipsia, and removal of the licking tube did not affect the frequency of aggressive episodes. 相似文献
13.
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
14.
The distribution of latencies and interresponse times (IRTs) of rats was compared between two fixed-interval (FI) schedules of food reinforcement (FI 30 s and FI 90 s), and between two levels of food deprivation. Computational modeling revealed that latencies and IRTs were well described by mixture probability distributions embodying two-state Markov chains. Analysis of these models revealed that only a subset of latencies is sensitive to the periodicity of reinforcement, and prefeeding only reduces the size of this subset. The distribution of IRTs suggests that behavior in FI schedules is organized in bouts that lengthen and ramp up in frequency with proximity to reinforcement. Prefeeding slowed down the lengthening of bouts and increased the time between bouts. When concatenated, latency and IRT models adequately reproduced sigmoidal FI response functions. These findings suggest that behavior in FI schedules fluctuates in and out of schedule control; an account of such fluctuation suggests that timing and motivation are dissociable components of FI performance. These mixture-distribution models also provide novel insights on the motivational, associative, and timing processes expressed in FI performance. These processes may be obscured, however, when performance in timing tasks is analyzed in terms of mean response rates. 相似文献
15.
William S. Maki 《Learning & behavior》1975,3(4):312-316
In a study of sustained attention (“vigilance”), pigeons performed a conditional discrimination in a 3-key operant chamber. Pecking a white center key initiated a 0.2- or 2.0-sec cue (a red or green disk). The side keys then displayed white disks, and a peck on the right or left key was reinforced depending on whether the preceding cue was red or green. Pecks on the white center key initiated the cue according to one of two schedules of cue production (FR 1 or VI 7.5 sec). Control of side key choices by 0.2-sec cues was disturbed by transition from FR 1 to VI 7.5, and recovered after the schedule of cue production changed from VI 7.5 back to FR 1. Control of choices by 2.0-sec cues was not affected by changing schedules of cue production. Rates of pecking the cue were higher than rates of cue-producing responses. 相似文献
16.
Terry W. Belke 《Learning & behavior》1992,20(4):401-406
Four pigeons were exposed to multiple schedules with concurrent variable interval (VI) components and then tested for preference transfer. Half of the pigeons were trained on a multiple concurrent VI 20-sec, VI 40-sec/cuncurrent VI 4G-sec5 VI 80-sec schedule. The remaining pigeons were trained on a multiple concurrent VI 80-sec, VI 40-sec/concurrent VI 40-sec, VI 20-sec schedule-After stability criteria for time and response proportions were simultaneously met, four preference transfer tests were conducted with the stimuli associated with the VI 40-sec schedules. During the transfer tests, each pigeon allocated a greater proportion of responses (M=0,79) and time (M=0.82) to the stimulus associated with the VI 40-sec schedule that was paired with the VI 80-sec schedule than lo the VI 40-sec schedule stimulus paired with the VI 20-sec schedule. Absolute reinforcement rates on the two VI 40 sec schedules were approximately equal and unlikely to account for the observed preference. Nor was the preference consistent with the differences in local reinforcement rates associated with the two stimuli. Instead, the results were interpreted in terms of the differential value that stimuli acquire as a function of previous pairings with alternative schedules of reinforcement. 相似文献
17.
Reed P 《Learning & behavior》2011,39(1):27-35
Binge eating is often associated with stress-induced disruption of typical eating patterns. Three experiments were performed
with the aim of developing a potential model for this effect by investigating the effect of presenting response-independent
stimuli on rats’ lever-pressing for food reinforcement during both fixed-interval (FI) and fixed-ratio (FR) schedules of reinforcement.
In Experiment 1, a response-independent brief tone (500-ms, 105-dB, broadband, noisy signal, ranging up to 16 kHz, with spectral
peaks at 3 and 500 Hz) disrupted the performance on an FI 60-s schedule. Responding with the response-independent tone was
more vigorous than in the absence of the tone. This effect was replicated in Experiment 2 using a within-subject design, but
no such effect was noted when a light was employed as a disrupter. In Experiment 3, a 500-ms tone, but not a light, had a
similar effect on rats' performance on FR schedules. This tone-induced effect may represent a release from response-inhibition
produced by an aversive event. The implications of these results for modeling binge eating are discussed. 相似文献
18.
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
19.
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
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