首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 31 毫秒
1.
In two experiments using the shuttlebox apparatus and negative (shock) reinforcement, goldfish learned to discriminate between same color signals differing only in brightness and to choose the brightness level paired with shock-omission to avoid shock. Experiment 1 compared two signal presentation procedures, one presenting only one signal at a time but allowing for successive alternation of signals within a trial (SUC) and the other presenting both signals simultaneously (SIM). SIM performance was superior to SUC in acquisition and showed more positive transfer with signal color changed (CC), more negative transfer with brightness-level—shock pairing reversed (R), and, although attenuated, more negative transfer with both signal color changed and shock pairing reversed (CC + R). Further, SIM relearning following reversal was faster than SUC. In Experiment 2, using the SIM procedure, eight transfer groups were tested for transposition with one of their original acquisition signals replaced in transfer by a signal bearing either the same or the opposite brightness relationship to the retained signal. Four transfer groups showed positive and four showed negative transfer effects, but all eight groups showed transfer performances consistent with a transpositional expectation. The present two experiments alone do not elucidate the mechanisms accounting for either the SIM superiority over SUC in Experiment 1 or the transposition effect in Experiment 2. These experiments show only that the transposition phenomenon can be supported by negative reinforcement procedures, which has not been demonstrated before. Now that techniques exist for producing negatively reinforced transposition, work investigating the underlying mechanisms and comparing them with the mechanisms of positively reinforced transposition can begin.  相似文献   

2.
Four colors (red, yellow, green, and blue) were arranged in all possible two-color sets to determine if goldfish can discriminate between color sets associated with shock and color sets associated with safety/shock omission in a one-phase (linear presentation) discrimination-learning procedure. The results showed that goldfish learned to discriminate between two-color sets if set colors were natural categorical color-code mates (red = yellow and green = blue). When natural code mates were not in the same set, and therefore were paired with different shock consequents, no discrimination learning occurred, suggesting that goldfish, unlike pigeons, are not able to code colors arbitrarily. The method also allowed a measure of preference between colors within sets associated with safety/shock omission. Original-learning preference measures between colors in sets so associated showed that goldfish chose red over any other color, yellow over blue or green, and green over blue, despite the fact that both colors in any set were procedurally identical, implying that goldfish do discriminate between colors in the absence of explicit discrimination training. The goldfish that failed to discriminate between red/blue and green/yellow sets in original learning were transferred to red/yellow and blue/green color sets. In transfer, the color paired with safety/shock omission in original learning was preferred over the color paired with shock in original learning, which resulted in a reversal of original-learning color preferences for half the goldfish. The transfer color-preference results imply that the goldfish had associated specific colors with specific shock consequents, but the associations were not robust enough to support discrimination learning in the face of categorical color coding.  相似文献   

3.
Goldfish, trained in a shuttlebox with cues and shock controlled by a linear presentation procedure, learned to control prevailing cue states and shock, and thus to discriminatively avoid shock presentation. The linear presentation procedure, adapted for the shuttlebox from the sequence of cue presentation occurring in the Y-maze, utilized three cues on each trial, a trial-start (TS) cue, a shock-paired (S?) cue, and an unpaired (S+) cue. At trial onset (TS cue), the goldfish had 10 sec to respond. The first response produced, via response-contingent programming, either the shock-paired (S?) or unpaired (S+) cue, and subsequent responses produced alternation of S+ and S?. The shock was omitted only if the S+ cue state prevailed 10 sec after trial onset. AU other cue states (TS and S?) were paired with shock. Goldfish learned to respond and control the prevailing cue state so that the S+ cue prevailed at 10 sec posttrial onset for a variety of different color-cue combinations and also learned to reverse their originally learned cue preference when the color cues were reversed. The linear presentation procedure represents an alternative discrimination learning procedure that appears to be free of the interpretational problems encountered in training goldfish in the shuttlebox apparatus with other one- and two-stimulus procedures.  相似文献   

4.
Rats were trained in a light ON vs light OFF discrimination in operant chambers with food reinforcement. Following acquisition, extinction under conditions of no alternations between S+ and S? and under conditions of numerous alternations between S+ and S? were examined. In Experiment I, extinction in S+ or S? alone produced less responding to S+ and more responding to S? than extinction with regular alternations between S+ and S?. In Experiment II, 9, 39, or 79 alternations in extinction between S+ and S? produced no differences in responding. These results indicate that during extinction of a discrimination there is (a) sharpening of differential performance, (b) a difference between multiple- and single-stimulus procedures, and (c) little effect of different numbers of alternations.  相似文献   

5.
A conditioned suppression experiment with rats studied the development of two discriminations involving two conditioned stimuli, A and X. In one discrimination (AX+/A?), compound presentations of A and X signaled shock and presentations of A alone signaled no-shock. In the other discrimination (A+/AX?), A alone signaled shock and AX signaled no-shock. AX+/A? discriminations were learned more rapidly than their A+/AX? counterparts. These results, which resemble the feature-positive effect of Jenkins and Sainsbury (1969, 1970), are discussed in terms of Rescorla and Wagner’s (1972) theory of conditioning and also in terms of stimulus intensity mechanisms.  相似文献   

6.
To test the hypothesis that distinctive internal representations are associated with number of successively presented nonreinforcements, four investigations employed rats in a discrete trial runway task (go/no-go), in which the smaller number of nonreinforcements was a signal for reinforcement (S+ cue), the larger number of nonreinforcements was a signal for nonreinforcement (S? cue). Consistent with the hypothesis under test, discriminative responding increased as the numerical difference between the S+ and S? cues increased. These results are highly similar to those previously obtained employing the conventional extinction procedure. However, unlike extinction data, the present findings cannot be interpreted without reference to numerical representations because better experimental control was employed here than has been in conventional extinction investigations. It was suggested that rats are capable of enumerating, or counting, successive nonreinforcements and that the tendency of rats to enumerate all types of reinforcing events is of importance for understanding not merely extinction, but a wide array of learning phenomena.  相似文献   

7.
Goldfish, trained in the shuttlebox to avoid shock, were tested for the acquisition and extinction of a color-matching or a color-oddity conditional discrimination choice response, and then tested for reacquisition. Extinction affected the accuracy of the choice response but not the number of trials with response (response strength). Half of all groups were extinguished with changed signal colors, and half had the same signal colors experienced in acquisition. All groups had the same signal colors in reacquisition that they had experienced in acquisition. Changed-signal oddity groups decremented slightly faster than same-signal oddity groups, providing some support for a generalization decrement interpretation, but same- and changed-signal matching groups did not differ. All groups extinguished on the choice response by the end of extinction. All matching groups, and all oddity groups, regardless of their respective signal colors in extinction, reacquired at the same rate, and faster than in acquisition. These results imply conceptual generalization of extinction effects. Matching-trained groups were found to be slightly superior to oddity-trained groups in both acquisition and reacquisition. Comparisons of these results to positive reinforcement conditional discrimination extinction work, including some procedural suggestions, are made.  相似文献   

8.
After rats were trained on a multiple schedule with variable interval 30-sec reinforcement in both stimulus components, omission, yoked, and extinction procedures were applied in S? while the variable interval continued in S+. In S?, omission training reduced response rate faster and to a lower terminal level than either response-independent yoked reinforcement or extinction, which were approximately equivalent. In S+, the extinction group exhibited elevated response rates representing behavioral contrast, while the omission and yoked groups showed reduced response rates. These results attest to the effectiveness of omission training as a response elimination method. They also contradict theories which posit reduction of response rate in S? to be necessary and sufficient for behavioral contrast.  相似文献   

9.
Three experiments were conducted to demonstrate that the place where an organism has been, before the organism is moved to a place with aversive consequences, can also become aversive through classical conditioning. In Experiment 1, two groups of 8 mice were exposed to three different contexts in succession, with a single shock occurring in the third context. The distal context was a putative 3-min conditioned stimulus (CS) for freezing; the second context was a delay manipulation; and the unconditioned stimulus (US) occurred in the proximal context. The group delayed for 15 sec showed significantly more freezing to the distal CS context than did the group delayed for 3 h. In a second experiment, conditioning to the distal context was demonstrated with a discrimination procedure for 8 more mice by using two different distal contexts as CS+ and CS? for the proximal context with shock. On CS+ days, 3 min of exposure to the distal context was followed within 5 sec by placement in the proximal box where shock occurred, whereas on CS? days, exposure to a second distal context was followed immediately by return to the home cage. Very strong differences in freezing between the CS+ and CS? distal contexts were found in all 8 mice after 14 days of conditioning. In a third experiment, the discriminative procedure was repeated for 9 more mice, with two changes. More objective stabilometertype activity measures were substituted for observed freezing, and, in addition to the CS+ and CS? distal context trials, each mouse was also exposed to a third discriminative distal context, which was followed by 15 min in a delay chamber followed by shock in the proximal context. This discrimination procedure with the activity suppression measure again resulted in significant differences between the contexts. The CS+ context and the context followed by a 15-min delay did not differ, but both of them differed from the CS? context.  相似文献   

10.
In three experiments, we assessed the role of signals for changes in the consequences of cues as a potential account of the renewal effect. Experiment 1 showed recovery of responding following extinction when acquisition, extinction, and test phases occurred in different contexts. In addition, extinction treatment in multiple contexts attenuated context-induced response recovery. In Experiment 2, we used presentations of an extraneous stimulus (ES), instead of context shifts, and found that responding recovered from extinction only when the ES was presented both between acquisition and extinction and between extinction and test. In Experiment 3, we used a reversal learning design in which, during training, two cues were first paired with different outcomes, then paired with the alternative outcomes, and finally paired again with the original outcomes. In this experiment, presentation, just prior to testing, of an ES that had previously been presented between the different phases produced an expectation of reversal in the meaning of the cues.  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.
Prior research on Pavlovian-to-instrumental transfer has shown that when a CS previously associated with shock (AvCS+) is presented contingent upon a choice response to a discriminative stimulus for food reinforcement, it facilitates discrimination learning. Conversely, a response-contingent CS previously associated with the absence of shock (AvCS?) retards discrimination learning. To evaluate whether these findings reflect across-reinforcement blocking and enhancement effects, two experiments investigated the effects of appetitively conditioned stimuli on fear conditioning to a novel stimulus that was serially compounded with the appetitive CS during conditioned-emotional-response (CER) training. Although there were no differential effects of the appetitive CSs in CER acquisition, Experiment 1, using a relatively weak shock US, showed that a CS previously associated with food (ApCS+) retarded CER extinction to the novel stimulus, in evidence of enhanced fear conditioning to that stimulus. In addition, Experiment 2, using a stronger shock US, showed that a CS previously associated with the absence of food (ApCS?) facilitated CER extinction to the novel stimulus, in evidence of weaker fear conditioning to that stimulus. These results parallel traditional blocking effects and indicate not only that an ApCS+ and an ApCS? are functionally similar to AvCSs of opposite sign, but that their functional similarity is mediated by common central emotional states.  相似文献   

13.
Rabbits under high or moderate water deprivation received in Stage 1 either paired (CS+), unpaired (CS?), or no-tone/shock presentations, with the pairings being appropriate for nictitating membrane conditioning. In Stage 2, all groups were given paired tone and water deliveries for jaw-movement conditioning, while, in Stage 3, all group received the tone and shock paired together for membrane conditioning. In Stage 2, the previously established aversive CS+ suppressed jaw-movement conditioning under high deprivation, and membrane CR decrements were directly related to deprivation. Also in Stage 2, the aversive CS? raised jaw-movement conditioning under moderate deprivation. In Stage 3, membrane CR performance immediately returned in the aversive CS+ group. For the other groups, conditioning was faster under high, relative to moderate, deprivation; however, the initial membrane CR occurrence required more trials if unpaired presentations were used in Stage 1. These results suggest that CSs can acquire both opponent-process and associative effects expressed according to the prevailing training conditions.  相似文献   

14.
The effects of transitions from nonrewarded (N) to rewarded (R) trials (N-R transitions) on discriminative behavior in differential conditioning and subsequent resistance to extinction were investigated in two experiments. In Experiment 1, groups given N-R transitions within S+ were more resistant to discrimination (ran fast in S?) and extinction than were groups given a partial reinforcement (PRF) schedule in S+ devoid of N-R transitions. Experiment 2 indicated that N-R transitions that occur when an N trial in S? is followed by an R trial in S+ are as effective in increasing resistance to discrimination, but not resistance to extinction, as are N-R transitions that occur within S+. The sequential effects obtained here were highly similar to those in conventional PRF and support the view that differential conditioning and PRF are highly interrelated phenomena. The results are discussed in terms of the extension of sequential theory to differential conditioning and the importance of internal reward-produced cues in discrimination learning.  相似文献   

15.
Rats trained in one context to use stimuli arising from food deprivation as discriminative signals for shock were tested in other contexts to assess the basis of conditioned responding (i.e., freezing or behavioral immobility). In Experiment 1, discriminative control by 24-h food-deprivation cues failed to promote transfer responding in a test context that had no association with shock. This indicated that food deprivation cues had little direct excitatory power. However, transfer of behavioral control by 24-h food-deprivation cues was obtained in a context paired with shock only when the rats were 19 h water deprived. This finding agrees with the idea that food-deprivation cues become conditioned modulators of the capacity of external stimuli to activate their association with an unconditioned stimulus. In Experiment 2, rats trained to use 24-h food-deprivation cues as signals for shock exhibited significantly greater transfer performance when the transfer context had undergone partial extinction relative to when the transfer context had undergone only simple excitatory training. This finding with deprivation cues and transfer contexts (1) paralleled earlier results obtained with discrete (auditory and visual) conditioned modulators and transfer targets, and (2) posed difficulties for associative summation and generalization interpretations of transfer performance.  相似文献   

16.
Following classical conditioning to a shock-reinforced tone CS (T1+), heart rate (HR) of three groups of rats was examined in response to a new reinforced tone (T2+) and a nonreinforced light (L?) CS given during conditioned inhibition (T2+ vs. T1L?), discrimination conditioning (T2+ vs. L?), or explicitly unpaired (T2/L? vs. US alone) procedures. Decelerative HR reactions occurred to the reinforced T2+ and T2+ CSs. To the respective nonreinforced CSs, the conditioned inhibition group displayed diminished but sizable HR deceleration, the discrimination group showed near-zero responding, and the explicitly upaired group showed HR acceleration. Subsequent reversal conditioning to L was retarded in the conditioned inhibition and explicitly unpaired groups relative to the discrimination group. Group differences on combined-cue [T2/L?) trials were not found. Both the HR responses during inhibitory training and the reversal-conditioning impairments suggest that inhibition may have been established to L? in the conditioned inhibition and explicitly unpaired groups.  相似文献   

17.
Two groups of kittens received 0 or 112 overtraining trials after learning a brightness discrimination. Both groups underwent extinction of differential choice responses and then learned the reversed brightness discrimination. The overtrained and nonovertrained animals did not differ significantly in rate of reversal learning, and both groups showed a significant preference for the old positive stimulus when differential reinforcement was reinstated in reversal training. According to Sutherland and Mackintosh, these results show that kittens lack stable attention and should be inept in dealing with reversal and probability problems. This is not the case, raising doubts about the adequacy of their account of interspecies differences in learning by vertebrates.  相似文献   

18.
In two experiments, the effects of feature identity in operant serial feature-positive discriminations were examined with rats. Rats were trained with two serial feature-positive discriminations (F1 → T1+/ T1? and F2 → T2+/ T2?), in which different operants were reinforced with delivery of a sucrose solution during two auditory target cues (T1 and T2). The features (F1 and F2) were two visual cues, two flavored sucrose solutions, or one visual cue and one sucrose solution. Transfer of a feature’s control to the target of the other discrimination was observed only when the features were from the same modality. When observed, transfer responding was of the form originally trained to the target, rather than the feature, and was preserved after feature extinction. Control groups showed that the differential transfer was not solely the consequence of differential feature generalization. Implications for theories of occasion setting are discussed.  相似文献   

19.
Goldfish, trained in the avoidance shuttlebox with a variant of the linear discrimination procedure, learned to conditionally discriminate between color signals, both for the matching (M) and oddity (O) criterion forms. Transfer to assess the possibility of concept learning was also tested. In original learning, oddity-trained groups learned faster and reached higher conditional discrimination performance levels than did matching-trained groups. In transfer, various groups were tested with the same criterion (MM or OO) or a shifted criterion (MO or OM), and half of each group retained the same color signals and the remaining half had its color signals changed in transfer. Groups with the same criterion in original learning and transfer (MM or OO), regardless of signal colors, showed comparable positive transfer. Groups with their criterion shifted between original learning and transfer (MO or OM) showed comparable negative transfer, regardless of signal colors. Since both positive- and negative-transfer effects were independent of signal colors, it is clear that what was learned for one set of signal colors transferred to at least one other signal-color set. These findings are consistent with the interpretation that goldfish learned the original conditional discrimination at a conceptual level, and learned about the general matching or oddity relationships between colors, rather than about a specific set of colors.  相似文献   

20.
Rats were trained to criterion (CT) and overtrained (OT) on a horizontal against vertical stripes discrimination in the jumping stand. A change in response strategy, from inspecting both stimuli to inspecting just the S?, was observed during overtraining. Replacing the S? with a novel stimulus disrupted performance in the OT Ss, but replacing the S+ did not. Performance in the CT Ss was disrupted, but not very severely, both when the S+ was replaced and when the S? was replaced. These results suggest that OT Ss in the jumping stand come to rely especially upon the S?. The overtraining effects found here are compared with those found in other types of apparatus.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号