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1.

If rats chose S+ in a brightness discrimination in a T-maze, they experienced, on that run and over four forced runs to S+ which followed, a pattern of reinforcement in which quantity of reward in the goalbox increased from 0 to 14 food pellets, decreased from 14 to 0 food pellets, or varied randomly. If the rats erred and chose S?, reinforcement was withheld, and they were forced a second time to 0 reward in the S? goalbox. The results indicate that rats readily learn the brightness discrimination under these conditions, the animals exposed to the sequentially increasing pattern learning somewhat slower than the others. This was true in spite of substantial delay of reward. Theoretical accounts based on perseverative inhibitory or facilitatory tendencies, or upon frustration, fail to describe the data accurately. Instead, analysis of the data shows that the animals were accurately anticipating the quantity of reward to be obtained on each run, running fast for large quantities and slowly for small.

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2.
To demonstrate a facilitating stimulus effect, as opposed to an incentive effect, of food reward, rats were trained on an easy, light-dark discrimination with different amounts of reward for correct and incorrect responses (1-0, 2-0, 3-1, and 5-1 pellets, respectively), and with shock or no shock administered in the correct goalbox. Both errors and trials to criterion were fewer with a large reward differential (LRD: 2-0 and 5-1), as compared with a small reward differential (SRD: 1-0 and 3-1), but were not affected by the “base” reinforcement condition of either 1 or 0 pellets for the incorrect response. In addition, choice and arm speeds during early training were positively related to the combined, or average, number of pellets contingent upon both correct and incorrect responses, indicating a generalization of reward expectancies. Although shock uniformly suppressed arm speeds under all reward conditions, it facilitated discrimination learning in the SRD conditions. That such facilitation occurred only when the conditions of reward for correct and incorrect responses were relatively similar indicates that not only shock, but also food can function as a distinctive cue: As a stimulus selectively applied to one response, it can decrease the similarity of the alternatives, and, in this manner, it can faciltate performance.  相似文献   

3.
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   

4.
Four groups of rats were given six acquisition trials under continuous reward, continuous delay of reward, partial reward, or partial delay of reward, following which all Ss received continuous delay. It was found that the partial reward and the partial delay of reward groups were significantly more persistent during the shift phase than the continuous reward group. No differences were found over trials between either the two partial groups or between each one and the continuous delay group.  相似文献   

5.
In two differential conditioning experiments, groups of 10 rats each differed with respect to average reward and schedule of reward received in S+. Nonreward (N) occurred on all S? trials. In both experiments, extinction of responding to S? (resistance to discrimination) was extensively regulated by reward sequence and was largely independent of average reward. In Experiment 1, resistance to discrimination was a function of transitions from N to rewarded (R) trials (N-R transitions). In Experiment 2, resistance to discrimination was increased by large reward on the R trial of N-R transitions and decreased by large reward on the R trial of R-N transitions. These schedule effects on resistance to discrimination parallel the effects of comparable schedules on resistance to extinction following partial reinforcement. The results are discussed in terms of sequential theory, reinforcement level theory, and their implications for various schedule manipulations that have previously shown S? behavior to be inversely related to average reward in S+.  相似文献   

6.
Reactivity to a reward is affected by prior experience with the different reinforcer values of that reward, a phenomenon known as incentive relativity, which can be studied using the consummatory succesive negative contrast (cSNC) paradigm, in which the performance of animals that receive a 4 % sucrose solution after trials on which they were exposed to 32 % sucrose is compared with that of subjects that always receive the 4 % sucrose solution. The exploration of a novel open field can enhance or block the acquisition of associative and nonassociative memories. The effect of open field on cSNC has not yet been explored. The main result of the present study was that open-field exposure significantly modified the expression of cSNC. Exposure to an open field 1 h but not immediately before the downshift interfered with the expression of cSNC. These animals drank more of the downshifted reward than did controls that were not exposed to the apparatus, and this behavior persisted for up to three recovery trials. This phenomenon was observed even when the animals were given a more protracted preshift phase and when the discrepancy between the preshift and shift incentive values of sucrose were increased. An open field also interfered with incentive downshift when open-field exposure occurred 6 h before the downshift, and repeated exposure to the apparatus did not deteriorate this effect. The present study adds to a growing body of literature that indicates that open-field exploration can interfere with memory formation.  相似文献   

7.
In Experiment I, rats which were both hungry and thirsty were given a choice between a food reward and a water reward. The animals preferred food to water when the reward was delivered immediately, but preferred water to food when a 30-sec delay was imposed in the goalbox before the reward was received. Experiment II replicated the results of the first experiment and showed, in addition, that when the delay was imposed in a separate delay chamber devoid of differential goalbox cues, subjects preferred food to water, similar to the immediate group. The results were discussed in terms of an incentive value process and a competing response hypothesis.  相似文献   

8.
Rats were trained on a daily partial reward schedule of small magnitude of reward (S), nonreward (N), and large magnitude of reward (L), which began with SN or SSNN for all animals. The remainder of the daily schedule was defined by the factorial combination of the number of rewards (1 vs. 3) and the magnitude of reward (S vs. L). Following 18 days of such training, 20 trials of extinction were administered. It was found that increasing the number of rewarded trials in a partial reinforcement schedule decreased resistance to extinction. Furthermore, increased number of large-magnitude rewards reduced resistance to extinction to a greater extent than increased number of small-magnitude rewards.  相似文献   

9.
Pigeons’ performance of a delayed conditional discrimination with presence versus absence of conditional (sample) stimuli was examined in two experiments. The pigeons showed steeper retention functions with feature (i.e., presence) samples (either food or yellow) than with no-feature (i.e., absence) samples (either no food or no yellow). These results suggest that pigeons code features and respond only by default to test stimuli (comparisons) associated with no features. In contrast, the overall superiority of performance on no-feature-sample trials compared with feature-sample trials in both the food/no-food- and yellow/no-yellow-sample tasks was reversed at a 0-sec delay in the food/no-food-sample group, but not in the yellow/non-yellow-sample group. This difference in results with hedonic versus nonhedonic samples suggests that the crossover in delay performance on food/no-food-sample trials is produced by the formation of backward associations between the food-associated comparison stimulus and the food sample.  相似文献   

10.
Geier CF  Luna B 《Child development》2012,83(4):1262-1274
Inhibitory control and incentive processes underlie decision making, yet few studies have explicitly examined their interaction across development. Here, the effects of potential rewards and losses on inhibitory control in 64 adolescents (13- to 17-year-olds) and 42 young adults (18- to 29-year-olds) were examined using an incentivized antisaccade task. Notably, measures were implemented to minimize age-related differences in reward valuation and potentially confounding motivation effects. Incentives affected antisaccade metrics differently across the age groups. Younger adolescents generated more errors than adults on reward trials, but all groups performed well on loss trials. Adolescent saccade latencies also differed from adults across the range of reward trials. Overall, results suggest persistent immaturities in the integration of reward and inhibitory control processes across adolescence.  相似文献   

11.
Pigeons performed a version of delayed matching-to-sample in which different postsample cues signaled different trial outcomes. Cues to remember (R cues) signaled the usual comparison stimuli. Cues to forget (F cues) signaled either cancellation of comparison stimuli (comparison-omission) or presentation of a sample-independent discrimination (comparison-substitution). As assessed by occasional probe trials, F cues decreased matching accuracy during comparison-omission more than during comparison-substitution. The loss in accuracy of matching in F-cue probes was directly related to length of delays during comparison-omission but not during comparison-substitution. Because trials generally terminated in reward during comparison-substitution but not during comparison-omission, these findings were interpreted as suggesting the importance of end-of-trial reinforcement for the maintenance of short-term memory.  相似文献   

12.
We previously reported that chimpanzees were unable to optimally select the smaller of two candy arrays in order to receive a larger reward. When Arabic numerals were substituted for the candy arrays, animals who had had prior training with numerical symbols showed an immediate and significant improvement in performance and were able to select reliably the smaller numeric representation in order to obtain a larger reward. Poor performance with candy arrays was interpreted as reflecting a response bias toward the intrinsic incentive and/or perceptual features of the larger array. In contrast, the Arabic numerals represent numerosity symbolically and appear to promote response choice on the basis of abstract processing of numerosity, with minimal interference from the inherent properties of the choice stimuli. The present study tested the hypothesis that, for mixed symbol-candy choice pairs, the requisite processing of the abstract numeral may foster a mode of numerical judgment that diminishes the interfering incentive/perceptual effects of the candy stimuli. The results were consistent with this hypothesis. Whereas performance on candy-candy arrays was significantly below chance levels, performance on numeral-candy choice pairs was significantly above chance and comparable with performance on numeral-numeral pairs.  相似文献   

13.
In delayed matching-to-sample with pigeons, brief postsample cues signaled different trial outcomes. The normal comparison stimuli followed the cue to remember (R cue). In the comparison-omission procedure, comparison stimuli and reinforcement were omitted following the cue to forget (F cue). In the comparison-substitution procedure, comparison stimuli were replaced by a single stimulus and reinforcement for a single response following the F cue. Infrequent probe trials revealed that F cues disrupted matching, with the amount of accuracy loss dependent on the length of the cue-comparison delay. These results, however, were found only with the comparison-omission procedure (Experiment 1). Replacing the comparison stimuli with another simultaneous (unconditional) discrimination revealed no accuracy loss in F-cue probes (Experiment 2), even though choice latencies were again lengthened by F cues. These results suggest that, while the F cue interferes with performance at the time of a retention test by slowing choices, it also interferes with sample retention. Alternative models of the cuing effect and its apparent dependence on end-of-trial reward are outlined.  相似文献   

14.
Young adult and aged squirrel monkeys were tested on variations of a two-choice, spatial delayed-response task. Aged monkeys committed more errors than did young monkeys. However, the diminished accuracy of the aged monkeys was not attributable to a memory deficiency because the difference was independent of delay interval. Aged monkeys did not display less responsesequence variability and were no more likely to commit systematic errors than were young monkeys. When response accuracy decreased as a result of increased delay intervals, or absence of a predelay cue, both age groups increased the proportion of errors attributable to random responding; however, the proportion of errors attributable to systematic errors either decreased or remained constant.  相似文献   

15.
Six experiments on learning in honeybees were prompted by the possibility that results previously attributed to a difference in amount of reward (20- versus 5-μl drops of sucrose solution presented on colored targets) might be due at least in part to a difference in delay of reward attendant on greater difficulty in locating the 5-μ1 drops. Substantial reduction in the diameter of the targets, which was designed to facilitate location of the drops, impaired discrimination of the colors, perhaps because their salience was reduced in the process (Experiment 3). White dots used to mark the location of the drops on larger targets also impaired discrimination of the colors, which presumably were overshadowed by the dots (Experiments 1, 2, and 4). That the dots did not serve merely to equate delay but were themselves discriminated was demonstrated in Experiment 5, which produced as well the first indication of an effect of amount of reward uncontaminated by the possibility of differential delay: Animals trained with a 5-μl drop on a dotted target of one color and a drop of the same size on an undotted target of a second color preferred the dotted target, but animals trained with a 5-μl drop on a dotted target of one color and a 20-μl drop on an undotted target of a second color preferred the undotted target. In Experiment 6, with odors substituted for the colors on the assumption that they were less likely to be overshadowed by the dots, what could be interpreted as a pure amount effect was found again. Aside from their relevance to questions about the role of amount of reward, the results have some interesting implications for the theory of discriminative learning in honeybees.  相似文献   

16.
Working memory in a bottlenosed dolphin was tested in both indirect and direct auditory delayed-discrimination tasks in which a correct spatial response was conditional upon the nature of a preceding sound. In the indirect task, either one of two possible sounds was briefly presented. After a prescribed delay, the dolphin was cued to go either to a left-hand or right-hand paddle pair. Responses to the outer paddle of a pair were rewarded following sound A, and responses to the inner paddle of a pair were rewarded after sound B. In the direct delayed-discrimination task, only one paddle pair was used in each session. In both tasks, the delay interval between the discriminative sound stimulus and the opportunity for a spatial response was progressively increased over sessions until the animal failed to meet a specified performance criterion or self-terminated a session. Delay limits of about 30 and 60 sec were obtained in the indirect and direct tasks, respectively. The increase in delay limit in the latter task was attributable to the use of an overt mediational response during the longer delays. In both cases, however, the obtained delay limits fell considerably short of the 2- to 3-min limits obtained in auditory delayed-matching studies using the same test sounds and the same subject. The task differences indicate that working memory functions cannot depend upon memory of the predelay stimulus alone, but must be determined in part by additional processes.  相似文献   

17.
The literature relevant to incentive contrast effects is reviewed, with emphasis on the data published since the reviews by Black (1968) and Dunham (1968). Contrary to the evidence available for the earlier reviews, the current literature indicates that positive contrast is a reliable phenomenon. Its occurrence is facilitated by use of a constant delay of reward, use of a long runway, or possibly by a shift while a negative contrast effect, resulting from a previous shift, is still present in the animals’ behavior. Positive contrast also occurs in consummatory behavior when sucrose or saccharin solutions are shifted. Conditions that are ineffective in producing positive contrast are reviewed, as are the effects of numerous variables on both successive and simultaneous contrast. In addition, positive and negative contrast effects resulting from shifts in delay or percentage of reward, contrast resulting from shifts in sucrose, saccharin, or ethanol solutions, contrast in choice behavior, and transsituational contrast are reviewed. The relationship of the data to several theoretical interpretations of contrast is also considered.  相似文献   

18.
In Experiment 1, rats received single-alternation training with 32% or 4% sucrose reward (Phase 1) followed by a shift in reward from 32% to 4%, and vice versa (Phase 2). In Phase 1, high reward facilitated alternation performance over low reward. In Phase 2, performance on rewarded trials increased as reward increased but was unchanged as reward decreased. Performance on nonrewarded trials showed negligible effects of shifts in reward. In Experiment 2, rats received goalbox placements with 32% or 4% sucrose alternated with nonreward in Phase 1; and in Phase 2, they received alternation runway training with the same or the opposite reward from that of placements. Performance on rewarded trials was faster, the higher the reward in runway training; performance on nonrewarded trials was slower, the higher the reward in placements. In Experiment 3, Phase 1 provided placements with 64%, 32%, 16%, or 4% sucrose or dry mash alternated with nonreward; Phase 2 provided alternation runway training with dry mash reward. Alternation prerformance developed more rapidly, the higher the sucrose concentration in placements. Only 64% sucrose produced performance superior to that for dry-mash placements.  相似文献   

19.
Three groups of 12 rats received 25 pretraining trials to each future discriminandum employed in a subsequent differential brightness conditioning problem. Groups NR and RN received partial reinforcement (PRF) pretraining either with or without, respectively, transitions from nonrewarded to rewarded trials (N-R transitions). Group CRF received consistent reinforcement during pretraining. A fourth group (n=12), Group NP, received no pretraining. During discrimination learning, one-half of the rats in each group received all their daily S+ trials preceding their daily S? trials (+? sequence); the remainder of the rats received an intermixed sequence of trials to S+ and S? (+?+ sequence). Discrimination learning was faster under the +? sequence than under the +?+ condition, and discrimination learning was retarded in Group NR relative to the other three groups, which did not differ from one another, under both the +? and +?+ discrimination sequence conditions. The results are discussed with Reference to previous experiments demonstrating N-R transition effects on discrimination learning, a theoretical extension of sequential theory to discrimination learning, and the effects of nondifferential reinforcement prior to discrimination learning on learned irrelevance.  相似文献   

20.
In Experiment 1, four groups of subjects (n = 16 each) were exposed to the situational stimuli of a shuttlebox apparatus for 4 h. Subsequently, 200 two-way avoidance trials were administered (100/day) with either .3- or 1.6-mA shock and with either small or large reward (presence or absence of visual stimuli following the response). Avoidance performance was directly related to shock intensity on both days and to magnitude of reward on the 2nd day. In Experiment 2, four groups of subjects (n = 24 each) were given 4 h of exposure either to the situational stimuli of the shuttlebox or to a neutral box. Then, 10 two-way avoidance trials were given with 1.6-mA shock. Subsequently, subjects were allowed to escape from one of the shuttlebox compartments to an adjacent safe box. Following preexposure to situational stimuli, avoidance performance was superior whereas escape-from-fear performance was inferior. This latter finding demonstrated that less fear of situational cues was present during avoidance training in the preexposed condition. All of these results support the effective reinforcement theory, an extension of two-factor theory, which emphasizes the importance for avoidance learning of the amount of fear of situational cues present following a response.  相似文献   

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