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1.
A series of four experiments studied the retention of the response made on a just-preceding trial as a function of the presence, and amount, of food reward given on that trial. Rats were trained to alternate arm choices in a T-maze, and then were tested for alternation with 5- or 30-sec delays between runs. When the subjects had received prior experience with the reward amounts used in testing, larger rewards led to better retention than did small or no rewards. However, when reward omission first occurred during the test phase, it produced more alternation on the following trial than did reward presence. The results suggest that both reward amount and surprisingness determine short-term retention of responses paired with the rewards. 相似文献
2.
John D. Batson Michael R. Best Deborah L. Phillips Hemlata Patel Kevin R. Gilleland 《Learning & behavior》1986,14(3):241-248
Thirsty rats were trained to collect small water rewards from the end of each arm of an eight-arm radial maze. During these training trials and subsequent testing trials, the subjects were allowed to choose a maximum of eight arms. “Preference” for a target maze location was studied by noting when, in the sequence of eight choices, the target was selected. During testing, when one maze location was consistently devoid of water, rats decreased their preference for this arm over trials (Experiment 1). Similarly, rats that learned a saccharin-lithium association demonstrated lower preferences for a maze location that consistently held the conditioned saccharin solution. This was true for animals that received saccharin-lithium conditioning on the maze (Experiment 3A) and for animals conditioned to saccharin in a separate context (Experiment 3B). An increase in preference for a target maze location consistently containing a sweet chocolate milk solution was observed in animals that were water- and food-deprived (Experiment 2). These studies demonstrate that animals will modify their responses toward (preferences for) maze locations that predictably contain an altered reward. 相似文献
3.
Time-place discrimination has been shown reliably in several avian and insect species, but only occasionally in rats and fish. In the present experiments, we explored the effects of response cost on time-place discrimination by rats. In the first experiment, we increased the cost of making a choice and the cost of recovering from a wrong choice in two types of maze, a radial arm and a vertical maze. In the radial arm maze, we found only general place preference, whereas in the vertical maze, we obtained evidence of time-place discrimination. In the second experiment, we found that the proportion of rats showing time-place discrimination increased with the height and, therefore, the response cost of the vertical maze. These results suggest that rats do not automatically store and/or retrieve the time and place of reward events but that response cost is an important trigger for time-place discrimination. 相似文献
4.
Rats received Pavlovian aversive (shock) conditioning in which white noise was established for different groups as a CS+, CSO, or CS?. Then, in an appetitive T-maze discrimination, the CSs were presented contingent upon a designated correct response for which food reinforcement was factorially varied at 0, 1, 2, or 4 pellets. Although the CS+ suppressed and the CS? facilitated speed of running in the correct arm at the start of discrimination training, these effects extinguished rapidly and did not interact with reward magnitude. Furthermore, choice learning was faciltated by the CS+ and retarded by the CS?, with these effects being comparable for the 1- to 4-pellet reinforcement conditions, but absent for the 0-pellet condition. These findings are difficult to reconcile with a transfer interpretation positing a general signaling property of the CS and are better interpreted as across-reinforcement blocking effects: By predicting a preferred outcome (safety) comparable to the preferred outcome of food reinforcement, the CS? blocks (retards) the association of reinforcement and the SD; conversely, by predicting a nonpreferred (shock) outcome discrepant from the preferred food outcome, the CS+ “counterblocks” (enhances) the association of reinforcement and the SD. 相似文献
5.
Two experiments are described, which involved the investigation of interactions between the nature of the conditioned stimulus (CS) and the nature of the unconditioned stimulus (UCS) in producing signal-centered behavior. In Experiment 1, rats received response-independent heat reinforcement in a cold environment. For some groups, this heat UCS was signaled by presentations of a standard aluminum retractable lever; for other groups, it was signaled by a retractable lever covered in acrylic fur (furry lever CS). Only the subjects that received the furry lever CS paired with heat exhibited differential CS-contact behavior, when compared with unpaired, aluminum lever, and warm control subjects. In Experiment 2, hungry rats received pairings of either an aluminum or a furry lever with food (UCS). When compared with unpaired controls, only the subjects that received the aluminum lever paired with food showed differential signal-directed behavior; the subjects receiving the furry lever CS did not show differential contact with the CS, but instead exhibited differential food tray entry behavior during CS presentation. In the two studies, the signal-directed behavior exhibited by subjects resembled either thermoregulatory or feeding behaviors characteristic of rats. The results suggest that signal-directed behavior is determined by a complex interaction between the ecological relevance of the CS and the nature of the UCS—an interaction that can best be described in terms of a behavior systems model of conditioned responding. 相似文献
6.
The effects of food reward on rats’ behavior in radial and Dashiell tunnel mazes were examined in two experiments. In the first, with animals at ad-lib body weights, food reward reduced speed of movement at the food locations, but did not affect the patterns of movement in either maze. Exploratory efficiency in the Dashiell maze was unaffected by food reward, and spontaneous patrolling of the radial maze by the nonrewarded animals was comparable to the behavior, reported by others, of rats running for food reward on elevated eight-arm mazes. In the second experiment, with subjects maintained at 80% of ad-lib body weights, there was some evidence for “winstay” learning: food-rewarded rats in the Dashiell maze were relatively more active near the food locations than were the nonrewarded animals, and more rewarded than nonrewarded rats revisited all food locations in the radial maze. Nonetheless, exploratory efficiency in the Dashiell maze was unaffected by food reward, as was patrolling efficiency in the radial maze, which was again comparable to that of rats on elevated mazes. The similarity in behavior of rewarded and nonrewarded animals in these mazes implies that the major determinant of their behavior, whether or not food reward is provided, is a spontaneous tendency to avoid places recently visited. 相似文献
7.
SingleParamecium caudatum were conditioned by pairing ac-generated electric shock (US) with a vibratory stimulus (CS) produced by an auditory speaker. Naive paramecia subjected to shock reliably exhibited a backwards jerk and axial spinning similar to the avoiding reaction described by Jennings in 1904. Such responses did not occur initially to CS alone, but increasingly appeared during the CS period preceding shock pairing (delayed conditioning paradigm). Control subjects given the CS and UCS at the same intervals, but explicitly unpaired, did not show a sustained increase of responses to the CS alone. Short-term memory was demonstrated by subjects first conditioned and then presented CS alone during extinction. These subjects were readily reconditioned. Paramecia trained and stored for 24 h showed reliable memory savings as compared to stored control subjects. Other paramecia were differentially conditioned by training with two CSs. Following the recommendations of Rescorla (1967), a procedure was designed for truly random presentation of the CS and UCS as an additional control for pseudoconditioning. Single paramecia were conditioned with intervals between CSs randomly ranging from 8 to 32 sec. Control subjects received the same number of CSs and UCSs, which were administered independently and randomly during the same total session duration. Thus, CS and UCS were occasionally paired for control subjects. The responses to CS in the conditioned group were anticipatory conditional responses due to the pairing contingency and not wholly due to pseudoconditioning. 相似文献
8.
An attempt was made to disrupt memory for spatial information by interpolating a task of high similarity to the to-be-remembered task during a long retention interval. Rats were trained in an 8-arm maze in which choosing each arm without repetition was the optional strategy. A 4-h delay was imposed between the 4th and 5th choices. At various times during the retention interval, the rats ran a second identical maze located in another room. No evidence of retroactive interference was observed. In the second experiment, the rat was required to remember the interpolated spatial task during the retention test. This was accomplished by allowing the rat to make four choices in the first maze and then, after a variable period of time, four choices in the second maze. Four hours after exposure to each maze, retention was tested. Choice accuracy on the retention tests was high and equivalent on both mazes. Requiring the rat to remember which arms it had visited in a second maze did not impair memory for the first maze. These results demonstrate that rats can segregate spatial memories established in different contexts with considerable proficiency. 相似文献
9.
Two experiments demonstrated that transfer of training between CSs from different sensory modalities survived substantial reductions in responding to the first CS. In both experiments, animals received three stages of training. Stage 1 entailed CS-US training with a CS from one modality (e.g., light), and Stage 3 entailed CS-US training with a CS from another modality (e.g., tone). The experiments differed in treatment during Stage 2. In Experiment 1, animals either remained in their home cages or received unreinforced exposures to the first CS, which extinguished the original CR. In Experiment 2, the animals received either continued CS-US training or exposure to the CS and US but at a long interval (2,800 msec), which eliminated the original CR. As the baseline for detection of transfer effects, each experimental group had a control group that received Stage 1 training with a 2,800-msec CS-US interval, which produced minimal CR acquisition. The results of both experiments revealed substantial positive transfer across CS modalities regardless of the treatment during Stage 2. The transfer did not appear immediately on test presentations of the second CS in Stage 3. Rather, the transfer appeared as an enhancement in the rate of CR acquisition after reinforced training with the second CS had commenced. The results are discussed with respect to stimulus generalization, neutralization of background stimuli, and learning processes superordinate to specific associations. 相似文献
10.
Rabbits were trained in eyelid conditioning with a “backward” arrangement of unconditioned stimulus (UCS) followed by conditioned stimulus (CS). When such a CS was tested alone it was observed to produce substantial conditioned responding if the UCS had been arranged to be “surprising” during the backward pairings, but not if it had been arranged to be “expected.” The comparisons were made in a within-subjects design where the surprisingness of the UCS on the different pairing occasions was manipulated by preceding the UCS by discriminative CSs which were otherwise either never followed by the UCS (CS?) or consistently followed by the UCS (CS+). The results may have implications for the nonmonotonic course of responding seen during backward conditioning, as a UCS is at first surprising, but then expected on the basis of contextual cues. 相似文献
11.
Two experiments investigated transfer of the rabbit’s conditioned nictitating membrane response (NMR) from shorter to longer CS-US intervals in conjunction with a change in CS modality, for example, light to tone. In Experiment 1, three experimental groups received initial training with a 400-msec CS-US interval, which produced substantial CR acquisition, and three control groups received initial training with a 2,800-msec CS-US interval, which produced minimal CR acquisition. Subsequently, the experimental and control groups received training with an 800-, 1,800-, or 2,800-msec CS-US trace interval. At the same time, the modality of the CS was changed from tone to light (or vice versa). Experiment 2 contained three groups that received initial exposure to a 400-msec CS-US interval, a 2,800-msec CS-US interval, or just the experimental chambers. Subsequently, all three groups received training with an 800-msec CS-US interval in a different CS modality. The results of both experiments revealed substantial positive transfer across CS modalities from the 400-msec CS-US interval to the 800-msec CS-US interval. There was also significant transfer to the 1,800-msec but not the 2,800-msec CS-US interval. The transfer did not appear immediately on test presentations of the second CS. Rather, the transfer appeared as an enhancement in the rate of CR acquisition after reinforced training with the second CS had commenced. The results are discussed with respect to mechanisms of transfer and facilitation of trace conditioning. 相似文献
12.
Treatments that interfere with animals’ short-term retention (e.g., in delayed matching-to-sample) were studied using a spatial memory task. Rats performed in an eight-arm radial maze in which choosing each arm without repetition was the optimal behavior. Performances were interrupted between fourth and fifth choices for a delay of 15 sec to 2 min. A variety of events occurring during the delay interval did not disrupt memories for prior choices (as assessed by the accuracy of postdelay choices). The ineffective treatments included variations in visual and auditory environments, removal from the maze, food consumed during the delay, a distinctive odor added to the maze, or combinations of these manipulations. Additionally, performance on another spatial task (a four-arm maze) during the delay between Choices 4 and 5 did not interfere with performance in the eight-arm maze. These findings suggest that rats’ memories for spatial locations are immune to retroactive interference, at least within the range of conditions reported, and that the rat can successfully segregate memories for spatial locations established in different contexts. 相似文献
13.
Luís Gonzalo De la Casa Auxiliadora Mena Juán Carlos Ruiz-Salas Esperanza Quintero Mauricio R. Papini 《Learning & behavior》2018,46(1):49-59
Three experiments explored the link between reward shifts and latent inhibition (LI). Using consummatory procedures, rewards were either downshifted from 32% to 4% sucrose (Experiments 1–2), or upshifted from 4% to 32% sucrose (Experiment 3). In both cases, appropriate unshifted controls were also included. LI was implemented in terms of fear conditioning involving a single tone-shock pairing after extensive tone-only preexposure. Nonpreexposed controls were also included. Experiment 1 demonstrated a typical LI effect (i.e., disruption of fear conditioning after preexposure to the tone) in animals previously exposed only to 4% sucrose. However, the LI effect was eliminated by preexposure to a 32%-to-4% sucrose devaluation. Experiment 2 replicated this effect when the LI protocol was administered immediately after the reward devaluation event. However, LI was restored when preexposure was administered after a 60-min retention interval. Finally, Experiment 3 showed that a reward upshift did not affect LI. These results point to a significant role of negative emotion related to reward devaluation in the enhancement of stimulus processing despite extensive nonreinforced preexposure experience. 相似文献
14.
Michael L. Platt Elizabeth M. Brannon Tara L. Briese Jeffrey A. French 《Learning & behavior》1996,24(4):384-393
Golden lion tamarins (Leontopithecus rosalia) and Wied’s marmosets (Callithrix kuhli) exhibited adaptive differences in performance on several distinct memory tasks. On both an open-field analogue of a radial arm maze and a spatial delayed matching-to-sample task, the marmosets performed better than the tamarins after short (5-min) retention intervals, but only the tamarins continued to perform above chance after long (24- or 48-h) retention intervals. The marmosets also required less training than the tamarins did to learn a color memory task, but again only the tamarins performed above chance when the retention interval was increased to 24 h. The results of these experiments are consistent with predictions based on knowledge of the feeding ecology of these species in the wild and raise the possibility that they possess different visuospatial memory abilities specialized for tracking the spatial and temporal distribution of their principal foods. 相似文献
15.
Lynn J. Hammond 《Learning & behavior》1995,23(3):349-356
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
16.
Thirsty rats were allowed to choose between a striped arm of a T-maze that contained water and a black arm that contained a saccharin solution. After each exposure to the saccharin solution, half of the animals received a lithium chloride injection 1 min later and half received the same injection 30 min later. Comparable saline injections at these same delays were given after each exposure to the striped, water, arm. The results from saccharin aversion, spatial aversion, and instrumental learning tests generally supported the hypothesis that delayed reinforcement has a substantially greater negative impact on the acquisition of an instrumental response than it has on affective conditioning. 相似文献
17.
In Experiment 1, a group of rats were runway trained on each of two reward series for 32 days. The two series consisted of three runs, the first two of which were, respectively, rewarded and nonrewarded; the third run was rewarded in one series but nonrewarded in the other. A 40-min interval separated the two series; the first and second runs within the series were separated by a 10-min interval, whereas the second and third runs were separated by a 30-sec interval. The reward (and nonreward) events and temporal cues of the two series are designated R-NR/R-NN. A second group was similarly trained, with the exception that the 10-min interval separated the second and third runs (RN-R/RN-N). Both groups developed appropriate differential running on the third run of the two series, and the RN-R/RN-N animals ran appropriately (slowly) on the second run of both series. Appropriate Run 2 performance appeared in one half of the R-NR/R-NN animals (depending upon order of series presentation); the remaining half ran faster on Run 2 of the R-NR series than on the same run of the R-NN series, an effect currently termed interevent anticipation. A cue shift phase in which all within-series intervals were 30 sec showed that the temporal intervals were controlling performance before the shift. Experiment 2 showed that interevent anticipation appears when all within-series intervals are either 10 min or 30 sec from the beginning of training, suggesting that the elimination of interevent anticipation in Experiment 1 was due to the differential cuing of runs by the temporal intervals rather than the particular interval duration. The overall findings suggest that the similarity of Run 2 and Run 3 performance termed interevent anticipation may be due to a failure to discriminate the ordinal position of runs within a series. 相似文献
18.
Male albino rats were run in a discrete-trial two-bar operant analog of the double alley. Completion of a FR 4 response chain on the first bar was rewarded 50% of the time for the 12 experimental Ss, but was never rewarded for the 12 control Ss. Both groups received consistent reward at the end of a FR 4 chain on the second bar. Eighty-four trials were given at a rate of four trials per day. A significantly faster rate of responding on the second bar was found following nonrewarded first-bar ratios than following rewarded first-bar ratios. This frustration effect was not attributable to response depression, since the nonrewarded performance of the experimental group exceeded that of the control group. 相似文献
19.
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.
相似文献20.
Jonathan K. Fernand Haleh Amanieh David J. Cox Nicole R. Dorey 《Learning & behavior》2018,46(4):472-478
The reverse-reward contingency (RRC) task involves presenting subjects with a choice between one plate containing a large amount of food and a second plate containing a small amount of food. Subjects are then required to select the smaller of the two options in order to receive the larger-magnitude reward. The RRC task is a commonly used paradigm for assessing complex cognition, such as inhibitory control, in subjects. To date, the RRC task has not been tested with pet dogs as subjects, and it may provide insights to their ability to perceive quantities of differing magnitudes. Nine dogs were tested in an RRC task involving three conditions. In Condition 1, plates of food were presented, and the dogs were allowed to consume their choice. In Condition 2, plates with different-sized symbols resembling the quantities of food in Condition 1 were presented, and dogs received food quantities of the same size as their choice (e.g., a larger-magnitude reward for selecting the plate with the larger shape). In Condition 3, the same plates were presented, but dogs received a reverse-sized quantity of food, relative to their choice (e.g., a smaller-magnitude reward for selecting the plate with the larger shape). A novel addition here to the traditional RRC task was the inclusion of a third, empty (control) plate that was present throughout all conditions, and no programmed consequences were provided when that plate was selected. Our results were consistent with the previous RRC literature: All dogs developed and maintained a preference for the larger stimulus option across conditions. The use of symbolic representations did not ameliorate performance on the RRC task. Applied implications are discussed. 相似文献