共查询到20条相似文献，搜索用时 715 毫秒
1.
Gloria D. Eldridge Joseph J. Pear Laine J. Torgrud Blair H. Evers 《Learning & behavior》1988,16(3):277-284
Three pigeons were exposed to fixed-time (FT) 15 sec, fixed-interval (FI) 15 sec for performing an arbitrary response, a reversal back to FT 15 sec, and then extinction (no reinforcement). During each phase, a computer-controlled tracking system continuously recorded the position of the bird’s head as it moved freely in the experimental chamber. During the first exposure to FT 15 sec, all 3 birds developed a pattern of feeder-wall-directed behavior with occasional circular excursions from the feeder immediately following reinforcement. During FI 15 sec, all birds performed the arbitrary operant, which consisted of contacting a virtual target sphere near the rear of the chamber, and did not engage in feeder-wall-directed behavior. During the reversal back to FT 15 sec, the birds developed a behavior sequence consisting of moving in the direction of the target sphere after reinforcement, followed by feeder-wall-directed behavior prior to the next reinforcement. During extinction, either moves toward the target sphere or wall-directed behavior occurred separately, interspersed with reappearance of the two as a sequence, followed by cessation of both members of the behavior sequence. These findings indicate that prior reinforcement of an arbitrary response can affect the location and form of superstitious behavior that develops near the beginning of the interreinforcement interval, but that other factors (e.g., immediacy of reinforcement) affect the location and form of the behavior near the end of the interval. The findings can be interpreted in the context of superstitious chaining. 相似文献
2.
Consumption of food pellets was examined in four water-deprived rats during 1-h sessions in which water was presented once every 30, 60, or 120 sec independently of the rats’ behavior according to three fixed-time (FT) schedules. Correlated with each FT condition was a continuous reinforcement (CRF) control condition in which the rats received, at the start of the session, the number of dipper presentations that were programmed to occur during the corresponding FT condition. During both the FT and CRF conditions, pellets per dipper presentation decreased and food intake rate increased with rate of water presentation, and there was a direct linear relation between log food intake and log water intake. For each of these three measures there was less eating under the FT condition than under the CRF condition, but the difference between the FT and CRF functions decreased at shorter FT values. These data are discussed in terms of the effects of amount of water on food consumption and the principle of temporal summation. 相似文献
3.
Pigeons were exposed to a two-component multiple fixed-ratio X fixed-ratio Y schedule of reinforcement in which X was always less than Y. Components were equal in duration and alternated at rates that varied between 2 sec and 23.5 h. Relative response rate in the FR X component: (1) increased as the duration of components increased between 2 sec and 15 min, (2) was at a maximum between 15 min and 6 h, and (3) decreased as the duration of components increased from 6 h to 23.5 h. The changes in relative response rate were attributable primarily to changes in absolute response rates during the FR Y schedule as absolute response rates during the FR X schedule were relatively invariant. These results pose complexities for several theoretical formulations. 相似文献
4.
Ben A. Williams 《Learning & behavior》2002,30(1):1-20
Behavioral contrast is defined as a change in response rate during a stimulus associated with a constant reinforcement schedule,
in inverse relation to the rates of reinforcement in the surrounding stimulus conditions. Contrast has at least two functionally
separable components: local contrast, which occurs after component transition, and molar contrast. Local contrast contributes
to molar contrast under some conditions, but not generally. Molar contrast is due primarily to anticipatory contrast. However,
anticipatory contrast with respect to response rate has been shown to be inversely related to stimulus preference, which challenges
the widely held view that contrast effects reflect changes in stimulus value owing to the reinforcement context. More recent
data demonstrate that the inverse relation between response rate and preference with respect to anticipatory contrast is due
to Pavlovian contingencies embedded in anticipatory contrast procedures. When those contingencies are weakened, anticipatory
contrast and stimulus preference are positively related, thus reaffirming the view that the reinforcing effectiveness of a
constant schedule is inversely related to the value of the context of reinforcement in which it occurs. The underlying basis
of how the context of reinforcement controls reinforcement value remains uncertain, although clear parallels exist between
contrast and the effects of contingency in both Pavlovian and operant conditioning. 相似文献
5.
Bruce L. Brown Nancy S. Hemmes David A. Coleman Alison Hassin Eva Goldhammer 《Learning & behavior》1982,10(3):365-376
Control of pigeons’ keypecking by a stimulus-reinforcer contingency was investigated in the context of a four-component multiple schedule. In each of three experiments, pigeons were exposed to a schedule consisting of two two-component sequences. Discriminative stimuli identifying each sequence were present only in Component 1, which was 4, 6, or 8 sec in duration, while reinforcers could be earned only in Component 2 (30 sec in duration). Control by a stimulus-reinforcer contingency was sought during Component 1 by arranging a differential relation between Component 1 cues and schedule of reinforcement in Component 2. In Experiment 1, rate of keypecking during Component 1 varied with the presence and absence of a stimulus-reinforcer contingency. When a contingency was introduced, rate of keypecking increased during the Component 1 cue associated with the availability of reinforcement in Component 2. In Experiment 2, the stimulus-reinforcer contingency was manipulated parametrically by varying the correlation between Component 1 cues and Component 2 schedules of reinforcement. Responding in Component 1 varied as a function of strength of the stimulus-reinforcer contingency. The relatively high rates of Component 1 responding observed in Experiments 1 and 2 pose difficulties for conceptions of stimulus-reinforcer control based on probability of reinforcement. In these two experiments, the stimulus-associated probabilities of reinforcement in Component 1 were invariant at zero. An alternate dimension of stimulus-reinforcer control was explored in Experiment 3, in which Component 1 cues were differentially associated with delay to reinforcement in Component 2, while probability of reinforcement was held constant across components. When the stimulus-reinforcer contingency was in force, rate of responding in Component 1 varied inversely with delay to reinforcement in Component 2. In a quantitative analysis of data from Experiments 2 and 3, relative rate of responding during Component 1 was strongly correlated with two measures of relative delay to reinforcement. 相似文献
6.
K. Geoffrey White 《Learning & behavior》1973,1(4):297-301
Following 20 sessions of variable-interval 20-sec reinforcement in the presence of a single 45-deg line-tilt stimulus, three pigeons were trained to discriminate between line tilts of 45 deg correlated with variable-interval 20-sec reinforcement and line tilts of 15 deg correlated with extinction. A generalization test along the line-tilt dimension was administered following a criterion discrimination performance. Gradients derived in terms of relative frequency of response as a function of line tilt indicated strong external stimulus control and exhibited clear peak shift. From the interresponse time (IRT) distributions generated for responding to each test stimulus, probability of response conditional upon IRT (IRTs/Op) was derived as a joint function of line tilt and IRT. The IRTs/Op functions for responses following IRTs in 0.2-sec-wide classes from 0.2 to 1.0 sec and for responses following IRTs in the interval of 1.0 to 2.0 sec were similar to the relative generalization gradients and also exhibited peak shift. Few IRTs were greater than 2.0 sec. External stimulus control was established over responses terminating IRTs both longer and shorter than 1.0 sec. 相似文献
7.
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
8.
In Experiment 1, rats were allowed to acquire either schedule-induced drinking or schedule-induced wood-chewing behavior under a fixed-interval (FI) 60-sec schedule of food reinforcement, following which food was omitted from 20% and then 50% of interreinforcement intervals. Omission of food severely disrupted induced drinking but had relatively little effect on induced wood-chewing. Experiment 2 investigated wood-chewing as a function of reinforcement rate, using a range of FI schedules from 5 to 180 sec in duration. Both the amount of chewing per session and the relative time spent chewing were bitonically related to reinforcement rate. In Experiment 3, schedule-induced chewing that had been acquired under a response-dependent schedule was found to persist under a response-independent schedule. Induced wood-chewing resembles other induced behaviors in important respects, but quantitative differences are also apparent. 相似文献
9.
Food-deprived rats that receive intermittent delivery of small amounts of food develop excessive drinking--specifically, schedule-induced polydipsia (SIP). A main characteristic of SIP is its occurrence at the beginning of interfood intervals. The purpose of this study was to demonstrate that SIP can be developed toward the end of interfood intervals, in closer proximity to upcoming than to preceding food delivery. In Experiment 1, two groups were exposed to a fixed-time (FT) 30-sec food schedule with water available during the first or the last 15 sec of each interfood interval. Two additional groups, which had access to water throughout, were exposed to FT 30-sec or FT 15-sec schedules of food presentation. The FT 30-sec group with free access to water developed the highest level of intake; similar and intermediate levels were induced in all the remaining groups. In Experiment 2, three groups of rats were exposed to an FT 90-sec food schedule with water available during the first, the second, or the last 30 sec of each interfood interval. One additional group with access to water throughout was exposed to the FT 90-sec schedule of food presentation. The group with free access to water developed a higher level of consumption than did the other groups, but by the end of training none of the four groups showed statistical differences in polydipsic drinking. Results show that adjunctive drinking can be developed in proximity to upcoming food delivery even with long interfood intervals. 相似文献
10.
Frances K. McSweeney 《Learning & behavior》1978,6(4):444-450
Four pigeons pecked keys and pressed treadles for food reinforcers delivered by several variable-interval schedules of reinforcement. Then the subjects responded on several concurrent schedules. Keypecking produced reinforcers in one component, and treadle-pressing produced reinforcers in the other. The changeover delay, which prevented reinforcement after all switches from one response to the other, was 0, 5, or 20 sec long. An equation proposed by Kerrnstein (1970) described the rates of treadle-pressing and keypecking emitted during the variable-interval schedules. The k parameter of this equation was larger for keypecking than for treadle-pressing. The R0 parameters were not systematically different for the two responses. The rates of keypecking and treadle-pressing emitted during the components of the concurrent schedules correlated with, but were not equal to, the rates of responding predicted by Herrnstein’s equation and the subject’s simple schedule responding. The ratios of the rates of responding emitted during, and the ratios of the time spent responding on, the components of the concurrent schedules conformed to an equation proposed by Baum (1974), but not to Herrnstein’s equation. 相似文献
11.
Prior cuing treatments intended to alleviate the forgetting of a conditioned avexsion-to an odor were tested with 18-day-old rats. Previous experiments had shown that when such pups were conditioned with the use of a CS?/CS+ procedure, pretest presentation of the CS? or US, but not the CS+, alleviated the forgetting otherwise seen after a 3-h retention interval. In Experiment 1, it was determined that the forgetting was not alleviated if the GS? was either preceded or followed by presentation of the CS+, despite the fact that the CS?/CS+ ordering mimicked that of original conditioning. Experiment 2 was an examination of the balance of extinction and reactivation effects caused by presenting the CS+ for varying durations following the 3-h retention interval. The forgetting over this interval was alleviated if the CS+ was presented for 5 or 15 sec, but not 30 sec. With an increase in duration of exposure from 15 to 30 sec, the consequences of the CS+ as a prior cuing treatment apparently shifted from reactivation to extinction. Experiment 3 was a test of the interaction between the consequences of different lengths of CS+ exposure and the effectiveness of adding CS? to the CS+ as a reactivation treatment. The varied effectiveness of reactivation treatments is discussed interms of a change in stimulus conditions from training to reactivation. 相似文献
12.
In the present experiment, an attempt was made to extend the base of evidence for the assumption of the behavioral theory of timing that pacemaker rate is determined by reinforcement rate. Pigeons discriminated the first half from the second half of a 50-sec trial in a free-operant psychophysical procedure. Left-key responding was reinforced at variable intervals during the first 25 sec, and right-key responding was reinforced at variable intervals during the second 25 sec. The rate of “extraneous” reinforcers delivered at variable intervals following responses to a center key was manipulated independently of performance in the temporal discrimination. Quantitative estimates of pacemaker rate were not directly proportional to extraneous rate of reinforcement, whether extraneous reinforcers were available during the intertrial interval, the entire session, or the trial only. Instead, estimates of pacemaker rate were inversely related to the rate of extraneous reinforcement, which suggests that pacemaker rate is determined by the ratio of the rate of reinforcement for the timing response relative to other sources of reinforcement. 相似文献
13.
In three experiments with rat subjects, we examined the effects of trial spacing in appetitive conditioning. Previous research
in this preparation suggests that self-generated priming of the conditional stimulus (CS) and/or unconditional stimulus (US)
in short-term memory is a cause of the trial-spacing effect that occurs with intertrial intervals (ITIs) of less than 240
sec. Experiment 1 nonetheless showed that a trial-spacing effect still occurs when ITIs are increased beyond 240 sec, and
that the effect of ITI over 60–1,920 sec on conditioned responding is best described as a linear function. In Experiment 2,
some subjects were removed from the context during the ITIs, preventing extinction of the context. Removal abolished the advantage
of the long ITI, suggesting the importance of exposure to the context during the long ITI. Experiment 3 still produced a trial-spacing
effect in a within-subjects design that controlled for the level of context conditioning and reinforcement rate in the absence
of the CS. Overall, the results are most consistent with the idea that adding time to the ITI above 240 sec facilitates conditioning
by extinguishing context-CS associations—and possibly context-US associations—that otherwise interfere with CS-US learning
through retrieval-generated priming (see, e.g., Wagner, 1981). 相似文献
14.
In two experiments, pigeons' responding on an extraneous task was explicitly reinforced during delayed matching-to-sample
trials. In Experiment 1, red or green sample stimuli were followed by retention intervals of 0.2, 1, 4, or 12 sec, during
which pecks to a white center key were reinforced with 2.5-sec access to wheat according to extinction, variable-interval
30-sec, and variable-interval 15-sec schedules in different conditions. A proportion of .2, .5, .7, or .9 of subsequent red
or green choice responses that matched the sample were reinforced with 3-sec access to wheat. The result was that increasing
center key reinforcement, or reducing reinforcer probability, lowered overall accuracy. Initial discriminability fell, but
with no change in the rate of forgetting. In Experiment 2, initial discriminability was affected by extraneous reinforcers
that were contingent on center key pecking, but not by noncontingent reinforcers. A plausible conclusion is that initial discriminability
decreases when reinforcers strengthen competing behaviors. 相似文献
15.
The effects of different schedule requirements at reinforcement on patterns of responding by pigeons were assessed under conjunctive schedules with comparable response-number requirements, Under one conjunctive schedule (conjunctive fixed-interval fixed-ratio schedule), a response was reinforced after a 6-min interval had elapsedand a specific minimum number of responses had been emitted, Under a second conjunctive schedule, a response was reinforced after the 6-min fixed interval and upon completion of a tandem schedule requirement (conjunctive fixed-interval tandem schedule), This schedule retained the same required minimum number of responses as the first conjunctive schedule, but responses were never reinforced according to a fixed-ratio schedule; the tandem schedule was comprised of a fixed-ratio and a small (.1 to 10.0 sec) fixed-interval schedule, Under the conjunctive fixed-interval fixed-ratio schedule, responding was characterized by an initial pause, an abrupt transition to a high response rate, and a second transition to a lower rate that prevailed or slightly increased up to reinforcement, Under the conjunctive fixed-interval tandem schedule, pauses were extended, response rates were lower, and the initial high rate of responding was generally absent, The above effects depended upon the size of the fixed interval of the tandem schedule, The distinct pattern of responding generated by conjunctive fixed-interval fixed-ratio schedules depends upon occasional reinforcement of fixed-ratio responding and not merely on the addition of a minimum number of required responses. 相似文献
16.
Blocking was investigated in a free-operant procedure by presenting a response-contingent signal prior to reinforcer delivery. At issue was the way in which blocking effects previously reported with this procedure are related to conditioned reinforcement effects, also previously found with similar procedures. Signal presentation decreased response rate when delay of reinforcement was 0 or .5 sec, but the signal increased response rate when the delay of reinforcement was increased to 3 sec. Thus, which effect (blocking or conditioned reinforcement) occurred depended critically on the response-reinforcer interval. 相似文献
17.
Michael D. Zeiler 《Learning & behavior》1983,11(2):237-246
Two procedures involving differential reinforcement of the duration of fixed-ratio sequences required pigeons to choose between simultaneously available duration requirements. One variation demanded only that the ratio durations exceed a lower limit; the second entailed an upper limit as well. In the no-upper-bound conditions, ratio duration was influenced by the other choice option. The larger the difference between the two duration requirements, the more ratio duration in one component shifted in the direction of the other requirement. The upper-bound procedure weakened this interaction. The temporal differentiation equation—an equation that has successfully described the effects of single time requirements on a variety of species and response units—fit the present results when the functional time requirement was viewed as the weighted average of the component requirements. The weighting parameter determining the functional requirement was influenced by the presence or absence of the upper bound. As has proven generally the case in temporal differentiation experiments, behavior did not conform to Weber’s law. Instead, sensitivity decreased as time taken to complete the ratio increased. 相似文献
18.
Jonathan J. Beam Peter R. Killeen Lewis A. Bizo J. Gregor Fetterman 《Learning & behavior》1998,26(4):388-396
The behavioral theory of timing assumes that timing is governed by a pacemaker whose pulses move organisms from one state to the next, and that the speed of the pacemaker covaries with the rate of reinforcement in the experimental context. The goal of the present experiments was to clarify just what constitutes that context. In Experiment 1, pigeons responded on signaled fixed-interval 20-sec and 40-sec schedules of food reinforcement that were presented randomly within sessions (alternating condition) or between sessions (isolated condition). In Experiment 2, pigeons categorized the duration of a short or a long set of intervals in the alternating or the isolated condition. Performance in both experiments was under strong control by the signals, with scalar timing between long and short sets, but no significant differences between the alternating and isolated conditions. The context of reinforcement that determines pacemaker period can thus be specific to a particular timing task and signal. 相似文献
19.
Pigeons received variable-interval (VI) reinforcement for keypecking during randomized presentations of seven line-orientation stimuli forming a continuum ranging from horizontal (0 deg) to vertical (90 deg). Each line presentation lasted for 30 sec and was preceded and followed by 30-sec time-outs. After responding stabilized, only responding in the two extreme stimuli (0 and 90 deg) was reinforced. As discrimination training proceeded, strong behavioral contrast and dimensional contrast effects appeared. However, only marginal local effects (local contrast and local dimensional effects), exerted by one line-orientation component upon a second, appeared, indicating that behavioral and dimensional contrast may be independent of parallel local effects. An attempt was made to apply Blough’s (1975) quantitative model of operant generalization and discrimination to the present discrimination procedure. However, this model did not predict the generalization gradient shape that was experimentally obtained. This experiment also yielded two serendipitous findings: (1) Positive behavioral contrast appeared in an extinction-related stimulus (time-out) when other stimuli were switched from reinforcement to extinction (hitherto, positive behavioral contrast had been observed only in responding to a reinforcementrelated stimulus when other stimuli were switched from reinforcement to extinction), and (2) final responding was higher in the presence of an extinction stimulus that had always been an extinction stimulus than it was in the presence of other extinction stimuli that had previously been paired with VI reinforcement. 相似文献
20.
In one experiment, the rate and pattern of responding (head entry into the food cup) under different distributions of intervals
between food deliveries were examined. Separate groups of rats received fixed-time (45, 90, 180, or 360 sec), random-time
(45, 90, 180, or 360 sec), or tandem fixed-time (45 or 90 sec) random-time (45 or 90 sec) schedules of reinforcement. Schedule
type affected the pattern of responding as a function of time, whereas mean interval duration affected the mean rate of responding.
Responses occurred in bouts with characteristics that were invariant across conditions. Packet theory, which assumes that
the momentary probability of bout occurrence is negatively related to the conditional expected time remaining until the next
reinforcer, accurately predicted global and local measures of responding. The success of the model advances the prediction
of multiple measures of responding across different types of time-based schedules. 相似文献