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1.
Pigeons received variable-interval (VI) reinforcement for keypecking during randomized presentations of seven line-orientation stimuli forming a continuum ranging from horizontal (0 deg) to vertical (90 deg). Each line presentation lasted for 30 sec and was preceded and followed by 30-sec time-outs. After responding stabilized, only responding in the two extreme stimuli (0 and 90 deg) was reinforced. As discrimination training proceeded, strong behavioral contrast and dimensional contrast effects appeared. However, only marginal local effects (local contrast and local dimensional effects), exerted by one line-orientation component upon a second, appeared, indicating that behavioral and dimensional contrast may be independent of parallel local effects. An attempt was made to apply Blough’s (1975) quantitative model of operant generalization and discrimination to the present discrimination procedure. However, this model did not predict the generalization gradient shape that was experimentally obtained. This experiment also yielded two serendipitous findings: (1) Positive behavioral contrast appeared in an extinction-related stimulus (time-out) when other stimuli were switched from reinforcement to extinction (hitherto, positive behavioral contrast had been observed only in responding to a reinforcementrelated stimulus when other stimuli were switched from reinforcement to extinction), and (2) final responding was higher in the presence of an extinction stimulus that had always been an extinction stimulus than it was in the presence of other extinction stimuli that had previously been paired with VI reinforcement. 相似文献
2.
Thirty rats received 10 sessions of baseline training in which leverpressing was reinforced according to a variable-interval (VI) 60-sec schedule. Twenty-four of the subjects were then assigned to one of four groups that received five sessions of extinction, with groups being differentiated in a 2 by 2 factorial design on the basis of: (1) changes in stimuli accompanying transportation of subjects from home cages to the laboratory and placement in the apparatus, and/or (2) changes in contextual stimuli within the apparatus. During the sixth session of extinction, the transportational and contextual stimuli previously associated with baseline training were reinstated. The remaining six rats experienced changes in both transportational and contextual stimuli but were maintained on the VI 60-sec schedule of reinforcement. Changes in either transportational or contextual stimuli reduced resistance to extinction and spontaneous recovery, and substantial increments in responding occurred upon reinstatement of the transportational and contextual stimuli associated with baseline training. Evidence for summation of the two sources of stimulus change was obtained. Changes in transportational and contextual stimuli produced only a brief disruption in responding when reinforcement of leverpressing was continued. 相似文献
3.
H. D. Kimmel A. F. Brennan D. C. McLeod M. S. Raich L. I. Schonfeld 《Learning & behavior》1979,7(4):447-451
EightCebus albifrons monkeys received 25 sessions of discriminative operant conditioning of the skin conductance response (SCR), with colored lights as discriminative stimuli and with Sidman avoidance (SS-40 sec, RS-40 sec) scheduled during one light and response-contingent shock during the other, Discriminative stimulus segments were separated by 30-sec periods of time-out from shocks and lights, Two extinction sessions were run 3 months after training, Almost from the beginning of conditioning, the monkeys made significantly more unelicited skin conductance responses in the avoidance periods than in punishment, The monkeys’ heart rates also increased significantly, but there was no difference between avoidance and punishment, SCR frequency during extinction continued to differentiate significantly between avoidance and punishment, and there was a significant increase in this differentiation from the last conditioning session to the first extinction session, but the difference then reduced in the second session, The results indicated that monkey’s SCRs are influenced by instrumental reinforcement contingencies somewhat in the same fashion as those of humans. 相似文献
4.
Pigeons learned to peck a keylight (S2) when it was paired with a stimulus (S1) that already evoked keypecking. Control procedures showed that S2 acquired control over responding because it was paired with S1 and because S1 had a conditioning history, thereby supporting the claim that S2 was a second-order conditioned stimulus. Second-order conditioning occurred as rapidly when S1 was a keylight as when it was a tone. Test procedures showed that after second-order conditioning, responding to S2 was markedly debilitated by the extinction of responding to S1, indicating that the ability of S2 to evoke a response importantly depends upon the continued ability of S1 to do so. Our demonstration that directed motor action in the pigeon is susceptible to second-order conditioning suggests a new interpretation of conditioned reinforcement in instrumental learning. Our demonstration that the effectiveness of S2 depends upon the continued effectiveness of S1 indicates that S-S associations are formed in this version of the second-order conditioning experiment. 相似文献
5.
In an experiment with rats, an appetitive conditioning method was used to investigate the generality of the hypothesis that
extinction should arouse attention to contextual cues, resulting in all learning in that context becoming context specific.
Rats received appetitive conditioning with a tone either while extinction of a flasher occurred (Group With Extinction) or
while it did not (Group No Extinction). Half of each group was subsequently tested in extinction in the context in which training
had taken place or in a different context. The results revealed a three-way interaction of extinction and context with trials,
in a direction opposite to the one the hypothesis would suggest. When rats were tested in a different context, there was generally
better responding in Group With Extinction than in Group No Extinction. In the same context, there was generally lower responding
in Group With Extinction than in Group No Extinction. Subsequent testing showed an ABA recovery effect. Results are discussed
in terms of the challenges they pose for the revised retrieval theory presented by Callejas-Aguilera and Rosas (2011). 相似文献
6.
Subjects in six experimental groups (n = 16 each) received one-trial passive avoidance (PA) training in which shock was delivered upon movement from a white wooden
floor compartment to a black grid compartment. Then fear was extinguished (30 min) in the black compartment. After either
24 or 168 h, all the groups were treated in a room distinctively different from the training room. At each interval, one group
received a shock in an apparatus similar to the conditioning box, another received a shock in a dissimilar apparatus, and
another was placed in a neutral box. A PA test trial in the training apparatus indicated reinstatement of extinguished fear
in all the groups given a postextinction shock except the 24-h dissimilar group. Control groups revealed that the extinction
treatment was effective and that spontaneous recovery was not evident. The results were explained in terms of classical conditioning,
stimulus generalization, and the broadening (flattening) of stimulus generalization gradients with time. 相似文献
7.
Steven J. Haggbloom LaNeel Lovelace Vickie R. Brewer Shelia M. Levins James D. Owens 《Learning & behavior》1990,18(3):315-322
Event-generated memory refers to the memory of a reinforcement (R) or nonreinforcement (N) event from an immediately preceding trial;signal-generated memory refers to the memory of a temporally remote R or N, retrieval of which is generated by presentation of a signal with which the memory is associated (Haggbloom, 1988). In each of three experiments, Group Signal-R received runway discrimination training in Phase 1 to establish a stimulus as a signal for R, and partial reinforcement training in Phase 2. An extinction test measured learning about the memory of nonreward (SN)—learning that occurs when SN is retrieved on R trials that follow N trials. In Group Signal-H, those R trials were accompanied by the signal for R, a treatment we hypothesized would generate retrieval of the memory of reinforcement (SR) so that signal-generated SR would replace event-generated SN as the operative memory, thereby eliminating the increased resistance to extinction normally produced by PRF training. In each experiment, Group Signal-R was less resistant to extinction than was a control group conditioned to respond to-event-generated SN. Extinction was as rapid in Group Signal-R as it was in a consistent reinforcement control group (Experiment 1) and in a group given intertrial reinforcements to interfere with learning about SN (Experiment 3). Experiment 2 tested two alternative interpretations of the failure to learn about SN in Group Signal-R. Those alternatives were found to be less viable than the hypothesis that the signal for R actively recruited retrieval of a competing memory. 相似文献
8.
Pigeons were trained on a two-component multiple schedule in which each separate component consisted of a three-link chain schedule. After initial baseline training, the stimuli correlated with the terminal links of each chain were presented in a successive discrimination, with one stimulus continuing to be associated with reinforcement while responses to the alternative stimulus were extinguished. Subjects were then returned to the original chain schedule, but with extinction in effect in both components of the multiple schedule. In two separate experiments, extinction of initial-link responding was not affected by which terminal link had been extinguished during the separate discrimination training, indicating that devaluation of the terminal link was not transmitted directly to the initial link of the chain. There was also no effect of the devaluation procedure during the first session of testing on responding in the middle link of the chain, but an effect did develop with continued extinction of the entire chain when the terminal components were presented during extinction. When the terminal components were omitted, however, the latter effect did not occur. Also, when the terminal link was omitted, extinction occurred more rapidly in the middle component than in the initial component, indicating a backward pattern of extinction. 相似文献
9.
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
10.
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
11.
12.
Animals exposed to schedules of partial reinforcement are typically more resistant to extinction than are animals trained with continuous reinforcement. This is the partial reinforcement effect (PRE). Animals experienced with both partial and continuous schedules are often more persistent on the continuous schedule, yielding a reversed PRE. Both conventional and reversed PREs have been elusive with classical conditioning paradigms. The present experiment attempted to demonstrate between- and within-subject PREs using 50% and 100% autoshaping schedules. Presence or absence of a PRE depended on the behavioral measures used. Marked terminal group differences in acquisition produced a between-subjects PRE with absolute response levels but not with rate-of-change measures. Within subjects, only choice trial comparisons were sensitive enough to differentiate the two schedules. Acquisition data were inconsistent with most of the classical conditioning PRE literature, but consistent with results reported in the autoshaping literature. These discrepancies may reflect the operant-classical interaction in autoshaping. 相似文献
13.
Brett E. Polenchar Anthony G. Romano Joseph E. Steinmetz Michael M. Patterson 《Learning & behavior》1984,12(1):69-72
Unconditioned stimulus (US) intensity and duration were manipulated to determine their effects on cat hindlimb flexion conditioning. Seven consecutive days of acquisition training of a hindlimb flexor response to a tone conditioned stimulus (CS) were followed by 2 days of extinction. Eight animals in each of 12 groups received a 1-, 2-, 3-, or 4-mA, 60-Hz shock delivered to the right hindleg for 25, 50, or 100 msec as the US. Analysis of conditioned-response (CR) frequency indicated that conditioned responding was a positive function of both the intensity and duration of shock, although these variables did not interact with one another. CR latency and amplitude were decreased and increased, respectively, by increases in US intensity. The pattern of results reported here may support a contiguity notion of conditioning, and are discussed in the context of other conditioning preparations. 相似文献
14.
Mice were trained to avoid shock by leaving a startbox and traversing a straight alley. During the first extinction phase (Phase I), two groups were given 30 regular extinction (RE) trials, while another two received punished extinction (PE) trials in the center of the alley. During the last 50 extinction trials (Phase II), conditions were reversed for one of the two groups receiving the same treatment in Phase I. This resulted in two nonshifted groups (RE-RE and PE-PE) and two shifted groups (RE-PE and PE-RE). PE treatment led to higher running speed in both phases and reversed an extinction trend. Furthermore, punishment-induced facilitation was greater for the group receiving PE following RE than for the group receiving PE immediately after avoidance training.
相似文献15.
Water-deprived rats were given a single exposure to saccharin and LiCl, either paired or unpaired. Half the subjects then received three saccharin-only exposures (extinction) in the training enclosure, followed by a single LiCl-only presentation (unconditioned stimulus reinstatement) 8 days after conditioning. The remaining subjects received six saccharin-only exposures, followed by LiCl reinstatement 13 days after conditioning. In both cases LiCl reinstatement occurred outside the training/test context. Appreciable recovery from extinction was observed after the partial loss of taste aversion obtained with three extinction sessions and the 8-day conditioning-reinstatement interval, but not after the asymptotic loss of taste aversion obtained with six extinction sessions and the 13-day conditioning-reinstatement interval. Conditioned taste aversions appear to be similar to more traditional associations with respect to both extinction and reinstatement-induced recovery from extinction. The results are discussed with reference to the event-memory, contextual-conditioning, and facilitated-retrieval hypotheses of postextinction reinstatement effects. 相似文献
16.
In the present experiments, savings phenomena following a limited amount of initial acquisition and extended extinction were
examined. Experiments 1 and 2 compared rates of reacquisition following brief acquisition and various amounts of extinction
in conditioning of the rabbit’s nictitating membrane and heart rate response, respectively. Experiment 3 compared rates of
acquisition to a novel stimulus (e.g., light) following brief acquisition and various amounts of extinction to another stimulus
(e.g., tone). In addition, in Experiment 3 recovery of responding to the extinguished stimulus during acquisition to the novel,
cross-modal stimulus was examined. Experiments 1, 2, and 3 demonstrated that with a limited number of acquisition trials (1)
there was a graded reduction in the rate of reacquisition as a function of the number of extinction trials in both conditioning
preparations, (2) there was a graded reduction in the rate of cross-modal acquisition as a function of the number of extinction
trials, but (3), in Experiment 3, recovery of responding to the extinguished stimulus during cross-modal training of the novel
stimulus appeared uniformly robust even in the face of extended extinction. 相似文献
17.
David R. Thomas C. F. Hickis Raymond L. Jackson Robert J. Newlin 《Learning & behavior》1979,7(3):301-308
In Experiment 1, two groups (n = 10) of pigeons received 17 sessions of TD (true discrimination) or ND (nondifferential) training with line angles. Seventeen sessions of SS (single stimulus) training with a wavelength preceded this training and two followed it. Subsequent wavelength generalization testing in extinction revealed a sharper TD than ND gradient. This slope difference was evident from the very first test stimulus presentation and remained stable throughout testing. As a consequence of substantial overtraining, there was no reduction of response strength and no sharpening of generalization during testing for either group. In Experiment 2, two groups (n = 16) of pigeons received 10 sessions of TD or PD (pseudodiscrimination) training with line angles, followed by four sessions of SS training with a single wavelength. During this training and in subsequent wavelength generalization testing in extinction, brief blackouts separated stimulus presentations. Again, the TD group yielded the sharper gradient. Although responding weakened and the gradients sharpened during the test, these effects were comparable in the two groups. Furthermore, gradients based on the percentage of trials with at least one response showed the same TD-PD slope difference. This finding indicates that differential control over responding by response-produced feedback is inadequate to account for the TD-PD difference in generalization slope. Both experiments indicate that a purported difference in resistance to extinction is also an inadequate explanation. 相似文献
18.
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
19.
Three experiments demonstrated that, following the extinction of an established conditioned stimulus (CS; e.g., tone), the
pairing of an orthogonal stimulus from another modality (e.g., light) with the unconditioned stimulus (US) results in strong
recovery of responding to the extinguished CS. This recovery occurred to about an equal degree regardless of whether or not
initial training contained unambiguous stimulus—reinforcer relationships—that is, consistent CS—US pairings—or some degree
of ambiguity, including intramodal discrimination training, partial reinforcement, or even cross-modal discrimination training
(tone vs. light). Experiments 1 and 2 demonstrated that this recovery of responding was largely specific to the extinguished
CS, but moderate generalization to other stimuli from the same modality did appear. The results are discussed with reference
to alternative mechanisms applicable to learning-dependent generalization between otherwise distinct CSs. These models assume
that such generalization is mediated by either a shared response, shared reinforcer, shared context, or shared hidden units
within a layered neural network. A specific layered network is proposed to explain the present results as well as other types
of savings seen previously in conditioning of the rabbit nictitating membrane response. 相似文献
20.
Pavlov (1927/1960) reported that following the conditioning of several stimuli, extinction of one conditioned stimulus (CS) attenuated responding
to others that had not undergone direct extinction. However, this secondary extinction effect has not been widely replicated in the contemporary literature. In three conditioned suppression experiments with rats,
we further explored the phenomenon. In Experiment 1, we asked whether secondary extinction is more likely to occur with target
CSs that have themselves undergone some prior extinction. A robust secondary extinction effect was obtained with a nonextinguished
target CS. Experiment 2 showed that extinction of one CS was sufficient to reduce renewal of a second CS when it was tested
in a neutral (nonextinction) context. In Experiment 3, secondary extinction was observed in groups that initially received
intermixed conditioning trials with the target and nontarget CSs, but not in groups that received conditioning of the two
CSs in separate sessions. The results are consistent with the hypothesis that CSs must be associated with a common temporal
context during conditioning for secondary extinction to occur. 相似文献