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1.
Sixty female hooded rats received 70 shock-escape training trials with shock- and safeboxes similar or dissimilar to each other and nonshock (safebox) confinement durations of 5 sec or 20 sec. (Shockbox confinement duration prior to shock onset was 5 sec.) In each confinement condition performance under the similar shock/safe condition was reliably poorer than that under the dissimilar condition. Safebox confinement duration negligibly affected performance under the dissimilar condition, while in the similar condition increasing confinement duration reliably facilitated performance. Comparisons with control data suggest that facilitation of escape was due to the relative shock-safe confinement duration rather than to absolute safebox confinement.  相似文献   

2.
After one-way avoidance training, rats were exposed, during avoidance response prevention, to light (CS-only) presentations or to light-shock (CS-US) pairings. Subgroups were then given 1, 5, or 10 trials during which they could escape immediately (unrestricted) or after 5 sec (restricted) by means of the previously conditioned avoidance response from a simultaneous light-shock compound. All animals were then exposed to avoidance extinction. The number of unrestricted escapes increased responding for CS-only animals, but had no significant effect on the performance of CS-US animals. Nevertheless, resistance to extinction was considerably less for CS-only animals given 10 unrestricted escapes than for CS-US animals given one unrestricted escape. One restricted escape had no more effect than one unrestricted escape for either response-prevention group. However, 5 restricted escapes elevated responding for CS-only animals to the level of CS-US animals. Extinction responding for CS-US animals increased significantly only after 10 restricted escapes. Since CS-only animals showed no further increase, resistance to extinction once more was greater for CS-US animals. These results, together with the very brief unrestricted escape latencies of CS-only animals, support a greater role for Pavlovian extinction than for response competition in the facilitation of avoidance extinction by CS-only response prevention. The fact that 10 restricted escapes were required to elevate resistance to extinction for CS-US animals over that obtained with one unrestricted escape attests to the effectiveness of Pavlovian conditioning during avoidance response prevention in elevating CS aversiveness to a near ceiling level.  相似文献   

3.
Delayed termination of the warning signal following extinction responses has been shown to facilitate extinction of discriminative avoidance. In order to determine the relative roles in extinction of delayed termination per se and postresponse exposure to the warning signal, which is necessarily confounded with delayed termination treatment, seven groups of rats were first trained on a one-way avoidance task in which a buzzer served as part of the warning-signal complex. Then, on nonshock extinction trials, the buzzer (a) terminated immediately with a response and was not reinstated in the postresponse interval, (b) terminated immediately with a response and was reinstated for a 5- or 10-sec period 5 or 15 sec following the response, or (c) terminated 5 or 10 sec following a response (delayed termination). Results indicated that exposure to the buzzer at postresponse intervals greater than 5 sec following responses was critically involved in reducing resistance to extinction. This finding supports a conditioned relief interpretation of the delayed warning signal termination effect and is consistent with the effect of response prevention techniques on extinction.  相似文献   

4.
A recent study found that avoidance extinction is equally facilitated by response prevention (blocking) whether the latter involves CS-alone or CS-shock presentations. An experiment was performed to determine whether this result was due to the use of a lengthy shock (5 sec) during response prevention. Five groups of rats were extinguished: (1) without prior blocking, (2) after blocking with CS only, (3) after blocking with a lengthy (5 sec) CS-contingent shock, (4) after blocking with a brief (.5 sec) CS-contingent shock, or (5) after blocking with a brief (.5 sec) shock only. The group blocked with the brief CS-contingent shock was substantially more resistant to extinction than the other four groups. The unblocked group and the group blocked with brief shock only required more trials to extinguish than the groups blocked with CS only or with lengthy CS-contingent shock, but did not differ from each other. The groups blocked with CS only or with lengthy CS-contingent shock also failed to differ from one another. The data support a significant role for Pavlovian conditioning processes in the effect of response prevention upon avoidance extinction.  相似文献   

5.
In Experiment 1, rats received escape training in which an exteroceptive feedback cue occurred in the safe box, and safe-box confinement durations of 5 or 20 sec were combined orthogonally with shock-box confinement durations of 5 or 20 sec. Exteroceptive feedback reliably facilitated escape performance relative to no-feedback controls when safe-box confinement was relatively longer than shock-box confinement. Confinement duration also facilitated performance in the absence of exteroceptive feedback. In Experiment 2, escape training with or without feedback was followed by extinction either with the feedback condition of prior training or with the opposite feedback condition. Feedback presentations in extinction reliably increased responding. Feedback removal reliably decreased responding relative to feedback controls. Introduction of feedback in extinction reliably enhanced performance relative to no-feedback controls.  相似文献   

6.
The crabChasmagnathus granulatus reacts to a shadow passing overhead with an escape response that habituates after 30 trials and for 5 days at least. The effect of a wide range of different intertrial intervals (ITIs) (0, 9, 27, 45, 81, 135, and 171 sec) on theChasmagnathus long-term habituation (LTH) was evaluated at 24 h. Memory retention was estimated separately at two phases of a six-trial testing session: at first trial (the initial testing phase) and at the subsequent block of five trials (the retraining phase). A training of 30 trials with an ITI equal to or longer than 27 sec induced LTH at both testing phases, however, with a 0- or a 9-sec ITI, training wholly failed to build up LTH. When the number of trials was increased, a massed training (ITI=0 or 9 sec) induced LTH at retraining but not at initial testing. Thus, massed training produces LTH only at retraining, whereas spaced training (ITI ≥ 27 sec) produces LTH at both initial phase and retraining. An ITI shift from training to testing diminished or abolished retention at retraining regardless of the direction of the shift, thus suggesting that crabs acquire a memory of the trial-spacing at training. According to these results, it is postulated that LTH consists of two memory components: one produced by spaced training and expressed at both initial testing and retraining, and one yielded by massed training and expressed only at retraining. The possibility that the two components of LTH were differentially affected by cycloxemide and context shift is discussed.  相似文献   

7.
Goldfish trained to discriminate between signals paired with shock (S?) and signals paired with shock omission (S+) with a linear presentation procedure, originally learned (OL) to control the signal state of a shuttle box and showed a decided preference for the S+ signal. In Experiment 1, following OL, groups had one OL signal replaced (S+ or S?), both signals replaced (S+ and S?), or the OL signals reversed (S+ and S? reversed) and were then tested in a transfer training procedure. In transfer, groups with one signal replaced maintained discriminated performance at OL levels; the S+ replaced group was slightly superior to the S? replaced group on the first day of transfer. With both OL signals replaced, discrimination dropped to chance performance levels, whereas, with OL signal shock pairing reversed, discrimination performance dropped below chance levels. In Experiment 2, following OL, extinction procedures consisted of turning off the shocker (0% shock) or of shocking 100% or a random 25% of the trials. A fourth extinction procedure (R,) retained the trial start response-dependent shock-omission contingency, but shock differentiating the S+ and S? signals was eliminated entirely. Extinction of the S+/S? discrimination was measured both during extinction training per se and with reversal retraining of the S+/S? discrimination later. Groups for which the OL S+ was paired with shock during extinction extinguished on both measures, but groups for which the OL S? was paired with shock omission did not extinguish, especially as shown by the reversal test procedure. Theoretical implications and the implications for several conditioning procedures are discussed.  相似文献   

8.
One procedure which has been used to supplement extinction in order to produce faster and more complete response suppression is to provide reinforcement for some alternative response which is incompatible with the response undergoing extinction. When reinforcement for the alternative behavior is discontinued, however, substantial recovery of the original response has often been observed. The present set of experiments demonstrated that such recovery is best accounted for by a “response prevention” hypothesis rather than by a “discriminative cue” hypothesis. High-frequency reinforcement of alternative behavior during the first half of an extinction phase seems similar in effect to procedures which physically prevent rats from emitting the response programmed for extinction.  相似文献   

9.
In five conditioned taste aversion experiments with rats, summation, retardation, and preference tests were used to assess the effects of extinguishing a conditioned saccharin aversion for three or nine trials. In Experiment 1, a summation test showed that saccharin aversion extinguished over nine trials reduced the aversion to a merely conditioned flavor (vinegar), whereas three saccharin extinction trials did not subsequently influence the vinegar aversion. Experiment 2 clarified that result, with unpaired controls equated on flavor exposure prior to testing; the results with those controls suggested that the flavor extinguished for nine trials produced generalization decrement during testing. In Experiment 3, the saccharin aversion reconditioned slowly after nine extinction trials, but not after three. Those results suggested the development of latent inhibition after more than three extinction trials. Preference tests comparing saccharin consumption with a concurrently available fluid (water in Experiment 4, saline in Experiment 5) showed that the preference for saccharin was greater after nine extinction trials than after three. However, saccharin preference after nine extinction trials was not greater, as compared with that for either latent inhibition controls (Experiments 4 and 5) or a control given equated exposures to saccharin and trained to drink saline at a high rate prior to testing (Experiment 5). Concerns about whether conditioned inhibition has been demonstrated in any flavor aversion procedure are discussed. Our findings help explain both successes and failures in demonstrating postextinction conditioned response recovery effects reported in the conditioned taste aversion literature, and they can be explained using a memory interference account.  相似文献   

10.
In order to determine the importance of the development of expectancy of reward prior to partial reward trials; rats were given 20 continuously reinforced trials prior to 20 partially reinforced trials (CRF-PRF) and compared to Ss given only 20 partially reinforced trials (PRF). Control groups received 20 or 40 continuously reinforced trials (CRF-20, CRF-40) to determine the effect of differing numbers of acquisition trials. Results showed that terminal acquisition differences were minimal in the run segment of the alley and that Group CRF-PRF was more resistant to extinction than Group PRF, and both were more resistant to extinction than the CRF-20 and CRF-40 groups, which did not differ from each other. These results were interpreted as supporting the notion that the expectancy of reward on nonreward trials during partial reinforcement acquisition is a determiner of the magnitude of the partial reinforcement extinction effect.  相似文献   

11.
Extinction of a conditioned palatability shift preceded extinction of conditioned taste avoidance whether rats were tested using a within-subjects design or a between-subjects design. In each of two experiments, consumption of 0.1% saccharin was paired with either 20 ml/kg of 0.15 M LiCl or equivolume physiological saline on a single trial. In Experiment 1, on each of 10 extinction trials, rats were given a taste reactivity test immediately prior to a consumption test. In Experiment 2, half of the rats were extinguished by taste reactivity testing and half of the rats were extinguished by a consumption test on each of 10 extinction trials. In both experiments, the aversive reactions of gaping and passive dripping were extinguished in a single trial and the suppression of ingestive reactions was extinguished in 2 trials; however, extinction of taste avoidance required 4–5 trials. These results suggest that rats continue to avoid a lithium-paired flavor even when they do not have an aversion to the taste.  相似文献   

12.
In a series of four experiments with free-flying honeybees, individual foragers were trained with targets of two different colors that contained 5 or 20 μl of 50% sucrose solution. The two targets were singly presented in quasi-random sequences on each visit, with the amount of reward to be found on each target perfectly predictable from its color. The number of training visits (4–32) was varied both within and between experiments, and so also was the relative frequency of trials with the 5- and 20-μl targets (1:1, 2:1, 3:1, and 9:1). At the conclusion of training under each condition, unrewarded responses to the targets were measured in a 10-min extinction test, with the targets presented either separately to two different groups of animals (Experiment 1) or as a pair (Experiments 2–4). When the number of training trials with each target was the same (Experiments 1 and 2), the animals responded more in extinction to the 20-μl target than to the 5-μl target, although there was a decline in the overall level of responding to both targets (an overlearning-extinction effect) as the number of training trials increased. After nine times as many, or only three times as many, training trials with the5- μl target as with the 20-μl target, the animals responded more in extinction to the 5-μl target (Experiment 3); after twice as many training trials with the 5-μl target as with the 20-μl target, there was equal responding to both (Experiment 4). The preferences shown in the choice tests of Experiments 2–4 could be simulated rather accurately on the assumptions of a model previously developed to deal with the discrete-trials choice behavior of honeybees and the further assumption that associative strength grows at a rate increasing with amount of reward to an asymptote independent of amount of reward.  相似文献   

13.
A hurdle-jump escape response was employed to assess the laboratory rat’s aversion or attraction to different types of conspecific odor. Odorant donor subjects received 112 runway acquisition trials on a continuous reward schedule followed by 32 extinction trials, 112 acquisition trials on a 50% schedule of reward and nonreward followed by 32 extinction trials, or 144 “neutral” trials with no reward in the alley. Different groups of test subjects escaped from odor excreted by odorant subjects on (a) nonrewarded acquisition and extinction trials, (b) rewarded trials during continuous reinforcement, (c) rewarded trials during partial reinforcement, or (d) neutral trials; others escaped from a clean box. The principal findings were: (1) significant aversion to “odor of nonreward” appeared after the donor odorants had received 12 exposures to reward; (2) production of odor of nonreward by odorant subjects changed as a function of training experience with reward; (3) after repeated exposure to odor of nonreward, the escape response habituated; (4) greater or different odor excretion in extinction resulted from subjects trained on a continuous reward schedule than on a partial reward schedule. Relationships of the data to frustration theory were discussed, assuming that inferred differences in production of odor reflect differences in frustration reaction.  相似文献   

14.
In two experiments, resistance to satiation was compared with resistance to extinction. In Experiment 1, rats given initial trials in a straight-alley runway while satiated failed to show increased resistance to satiation in a later test phase. This negative finding contrasts with the increased resistance to extinction usually found following initial nonrewarded trials in a straight alley. In Experiment 2, rats were extinguished or were run while satiated following deprived acquisition, and then were either shifted to the other condition or maintained under the same condition. A greater response decrement was produced by extinction than by satiation, both when current performance was examined and when the persistent effect of satiation or extinction on later performance was examined. These results show that there are important dissimilarities in the effects of satiation and extinction, dissimilarities that suggest that extinction is more nonrewarding or aversive than satiation. It seems likely that extinction involves processes (such as frustration, arousal of aversive motivation, and conditioned inhibition) not involved in satiation, which account for the greater response decrement in extinction as compared with satiation.  相似文献   

15.
The effect of quantity and quality of reinforcement on performance change following a shift to uniform high reward was studied in four groups of rats. Twenty or 200 licks of a 5% or 20% sucrose solution constituted the four incentive conditions. Two additional subject groups were run in the high (20%–200 licks) and low (5%-20 licks) reward conditions to determine how amobarbital sodium, an emotional depressant, influences incentive shift performance. All six groups received 60 preshift runway trials (6/day), followed by 30 high reward trials. Twenty-four extinction trials contrasted drugged and normal performance relating to high and low reward Postshift positive contrast appeared in all nondrugged groups. An emotional base for positive contrast is considered.  相似文献   

16.
Two experiments assessed the role of aftereffect learning in rats rewarded with sucrose solutions. In Experiment 1, rats were trained in a single straight runway for two trials on each of 18 days, each trial terminating with either large (20% scurose) or small (3% sucrose) reward. The ITI was 3–5 min. The sequence of daily rewards for each of four groups was small-small (SS), small-large, (SL), large-small (LS), or large-large (LL). Response patterning and a simultaneous negative contrast effect were observed in LS and SL relative to the consistently rewarded controls. During 10 massed extinction trials, resistance to extinction was greatest for Group SL, followed in order by Groups SS, LL, and LS. Experiment 2 examined single alternation of large and small rewards administered for 10 trials on each of 31 days with an ITI of 60 sec. Reward for one group was 20% or 3% sucrose while another received 1 or 10 45-mg Noyes pellets. Appropriate patterning developed only in the food-pellet rewarded animals. The overall results suggest that sucrose rewards may produce high-amplitude and long-duration aftereffects which interfere with learning in designs employing several massed daily trials, but which may facilitate learning—relative to food-pellet rewards—with longer intertrial intervals and fewer daily trials.  相似文献   

17.
Rats trained to make an approach response with either nonreward or 150- or 175-V shock occurring on 2, 3, or 4 of 6 daily trials showed greater resistance to extinction than continuously reinforced-unpunished controls. Persistence during extinction was a function of both the type and the frequency of response-contingent event in acquisition. The significant interaction of these two factors was best interpreted as a result of the counterconditioning of the approach response (Amsel, 1972) to anticipatory conditions which varied in similarity to the frustrative nonreward of extinction.  相似文献   

18.
Resurgence is the recurrence of a previously reinforced and then extinguished behavior induced by the extinction of another more recently reinforced behavior. Resurgence provides insight into behavioral processes relevant to treatment relapse of a range of problem behaviors. Resurgence is typically studied across three phases: (1) reinforcement of a target response, (2) extinction of the target and concurrent reinforcement of an alternative response, and (3) extinction of the alternative response, resulting in the recurrence of target responding. Because each phase typically occurs successively and spans multiple sessions, extended time frames separate the training and resurgence of target responding. This study assessed resurgence more dynamically and throughout ongoing training in 6 pigeons. Baseline entailed 50-s trials of a free-operant psychophysical procedure, resembling Phases 1 and 2 of typical resurgence procedures. During the first 25 s, we reinforced target (left-key) responding but not alternative (right-key) responding; contingencies reversed during the second 25 s. Target and alternative responding followed the baseline reinforcement contingencies, with alternative responding replacing target responding across the 50 s. We observed resurgence of target responding during signaled and unsignaled probes that extended trial durations an additional 100 s in extinction. Furthermore, resurgence was greater and/or sooner when probes were signaled, suggesting an important role of discriminating transitions to extinction in resurgence. The data were well described by an extension of a stimulus-control model of discrimination that assumes resurgence is the result of generalization of obtained reinforcers across space and time. Therefore, the present findings introduce novel methods and quantitative analyses for assessing behavioral processes underlying resurgence.  相似文献   

19.
Four experiments test the hypothesis that escape learning in response to shock will transfer to a similar food-reinforced response and affect resistance to appetitive extinction. In the first two experiments, subjects were given escape training in a straight alley followed by continuous food reinforcement and then extinction. Prior escape training resulted in greater resistance to extinction of the food-reinforced response as compared to several control procedures. In the third experiment, the escape response was manipulated to be compatible or incompatible with the subsequent food-reinforced response. Greater resistance to extinction was shown when the two responses were compatible. The fourth experiment confirmed and extended this finding. The relationship of the present results to Amsel’s theory of persistence was discussed.  相似文献   

20.
In Experiment 1, hungry rats received 30 rewarded runway trials and then either extinction trials followed by retention tests or just retention tests. Different groups were tested after retention intervals of 1 min, 1, 3, or 24 h, or 30 days. Retention of extinction training was a nonmonotonic, cubic function of time for the early portion of the response chain, with good retention at 1 min and 3 h and little retention at 1 h, 24 h, or 30 days. In the latter portions of the response chain, retention of extinction decreased monotonically with time. Retention following reward-only training varied little in time, though slight losses occurred after 30 days. Experiments 2–3 differed from Experiment 1 in imposing nonchoice discrimination training (reward vs. nonreward) instead of extinction following 30 rewarded trials. After different time intervals (.017, .75, 1.25, 3, and 24 h in Experiment 1; and .017, 1, and 3 h in Experiment 2), retention tests revealed poorest discrimination at intermediate intervals in the initial portion of the response chain, i.e., a Kamin effect appeared. The deficit seemed the result of a loss of response suppression to the cue that signaled nonreward. In latter segments of the response chain, a Kamin effect tended not to appear. Implications for a number of observations and theoretical views are noted.  相似文献   

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