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1.
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   

2.
A modification of the nonlinear curve-fitting procedure proposed by Wetherington and Lucas (1980) was used to assess how well Herrnstein’s (1970) equation for the rates of responding during concurrent schedules described performance. The equation fitted some results very well, accounting for 80% or more of the variance in the data in studies that used moderate-duration changeover delays and provided the same positive reinforcers, operanda, and simple schedules in the two components. The equation fitted the data poorly in other studies. The k parameter changed with several variables; it was not as constant as Herrnstein (1974) suggested. R0 did not fit Herrnstein’s interpretation as reinforcement from unprogrammed sources. Forty percent of all values of R0 were negative, and another 23% were unreasonably large (greater than 50 reinforcers/h). The data suggest that Herrnstein’s equation is not a general theory of concurrent-schedule responding, and that Herrnstein’s interpretation of k and R0 should be modified.  相似文献   

3.
Four pigeons pecked for food reinforcement on variable interval 1-min schedules and on the variable-interval 1-min components of multiple, concurrent, and pseudoconcurrent schedules. The pseudoconcurrent schedule provided only one schedule of reinforcement; but, any reinforcer could be collected by responding on either of two keys. The rate of responding generated by the variable interval schedule was not greater than the rates of responding generated by the components of the complex schedules. But, the rate of reinforcement obtained from the variable interval schedule was greater than the rates of reinforcement obtained from the components of the multiple schedule. These results may contradict the equation proposed by Herrnstein (1970). The equation predicts that the rate of responding generated by a schedule of reinforcement will be greater when the schedule appears alone, than when it appears as one component of a complex schedule.  相似文献   

4.
Four pigeons pecked for food reinforcers delivered by several two-key concurrent schedules. The sum of the rates of reinforcement provided by the component schedules varied from 25 to 300 reinforcers/h. The ratio of the rates of reinforcement remained constant at 1:4. The sum of the rates of responding generated by the component schedules increased with increases in the sum of the rates of reinforcement which the components provided. The increase in response rate was predicted by equations proposed by Catania (1963) and by Herrnstein (1970). But the data conformed more closely to Herrnstein’s equation.  相似文献   

5.
Pigeons’ choice responding on 10-sec interpolated probes was studied after baseline training on multiple variable-interval variable-interval schedules of food reinforcement. Unreinforced choice following training with three different relative reinforcement rates (Experiment 1), with a 3-ply multiple schedule (Experiment 2), and with three different relative reinforcement durations (Experiment 3) was examined. Least squares lines were fit to choice relative response rate and schedule relative response rate as functions of training relative reinforcement rate; choice slope was significantly greater than schedule slope in all three experiments. This result is counter to the prediction of Herrnstein’s (1970) theory that these slopes should not differ. Luce’s (1959) theory also failed to account for the data. It was concluded that choice responding was controlled by both approach to the stimulus associated with the smaller mean interreinforcer interval or the longer duration, and avoidance of the other stimulus.  相似文献   

6.
Pigeons pecked keys for food reinforcers delivered by several variable-interval and multiple variable-interval schedules. The rates of responding emitted during the simple schedules were not systematically different from the rates emitted during the multiple schedules when the components of the multiple schedule were identical. The rates of responding emitted during the components were usually greater than the rates emitted during comparable simple schedules when the components were more favorable than the added components of the multiple schedules. Response rates during the components were not significantly lower than those during comparable simple schedules when the components were less favorable. The observation of higher rates of responding during the more favorable components conforms to a prediction of several additive theories (e.g., Rachlin, 1973) but violates a prediction of Herrnstein’s (1970) theory. However, the additive theories are brought into question by the fact that changing the location of the discriminative stimuli did not change the pattern of results.  相似文献   

7.
8.
Previous research that compared the estimated parameters (i.e.,k andR e) from Herrnstein’s (1970) hyperbolic matching law equation within the same individuals responding for qualitatively different consummatory reinforcers (i.e., water and sucrose solution) found similar asymptotic response rates (k). The present study compared these parameters within subjects responding on levers for consummatory and nonconsummatory reinforcers. Male Wistar rats responded on a lever in a running wheel on a series of tandem FR 1 VI schedules for either 0.1 ml of a 15% sucrose solution or the opportunity to run for 15 sec. Herrnstein’s hyperbola was fit to response and reinforcement rates from each session. Results showed thatk values were significantly higher for sucrose than for wheel-running reinforcement. On average,R e was lower for sucrose than for wheel-running reinforcement, though not significantly lower. The results of the present study appear to violate the assumption of the constancy ofk in Herrnstein’s matching law analysis.  相似文献   

9.
Five rats responded on several concurrent schedules in which pressing a key produced reinforcers in one component and pressing a lever produced reinforcers in the other component (Experiment 1). Four pigeons responded on several concurrent keypeck treadlepress schedules (Experiment 2). The programmed rates of reinforcement varied from 15 to 240 reinforcers per hour in different conditions. Rates of responding usually changed systematically within experimental sessions, and the changes were similar for the two components of a concurrent schedule. These results imply that within-session changes in responding may not confound the predictions of theories that describe the ratio of the rates of responding during the two components of concurrent schedules. Instead, within-session changes may be controlled by a mechanism that integrates the reinforcers obtained from the two components.  相似文献   

10.
Pigeons responded in a two-component peak procedure in which the components differed in terms of reinforcement magnitude (Experiment 1), immediacy (Experiment 2), or probability (Experiment 3). The prediction of behavioral momentum theory that responding in the relatively richer component should be more resistant to change was tested by (1) presenting response-independent food in the intervals between components according to a variable-time (VT) schedule, (2) prefeeding, and (3) extinction. In all the experiments, peak location in baseline occurred earlier, relative to the schedule value in the richer component. Peak response rate was more resistant to change in the richer component during the VT and prefeeding tests, and change in peak rate was more sensitive to differential reinforcement than change in overall response rate. Changes in measures of performance on peak trials during the disruptor tests were partially consistent with predictions of the behavioral theory of timing. The results suggest that peak response rate provides a more sensitive index of resistance to change for fixed-interval schedules than does overall response rate and that reinforcement strengthens both peak responding and temporal control.  相似文献   

11.
The conservation model was generalized to the variable-interval schedule by incorporating the concept of unscheduled instrumental responses, those which occur in the time before the next setup is due. Thirsty rats responded in constant-duration sessions on two 7-sec schedules that required one leverpress for 25 and 50 licks at a water tube and on a 14-sec 25-lick schedule. In accordance with the model, total licks decreased linearly as total presses increased, and the schedules facilitated leverpressing and suppressed licking relative to paired baseline levels of responding. While the matching model also gave a satisfactory fit to instrumental responding under the schedules, its two constants, representing asymptotic rate of responding and extraneous reinforcement, had anomalous values which led the model to predict that response rate would decrease as the rate of reinforcement increased, directly opposing its prediction for the constant-consumption experiments of its previous tests.  相似文献   

12.
Six rats were placed on concurrent variable-interval variable-interval schedules with a 15-sec changeover delay (COD). The variable-interval schedules were varied such that the COD comprised between 25% and 100% of the average interreinforcement interval of the more favorable alternative. The obtained reinforcement rate and the rate of changing from one schedule to the other were compared to predictions of Houston and McNamara’s (1981) optimality model of concurrent choice. The pattern of behavioral allocation was consistent with the predictions of the model, although none of the animals was able to achieve optimal performance on any of the presented schedules. Observed behavior reliably tracked optimal behavior in that the ratio of obtained reinforcers to the optimum predicted by Houston and McNamara did not vary as the underlying schedule parameters was changed.  相似文献   

13.
14.
In this investigation, which employed rats in a runway, discriminative responding consisted of faster running on the reinforced than on the nonreinforced trials of either the 4NR or R4N schedule, both schedules containing fixed, repeated sequences of nonreinforced and reinforced trials. Under the 4NR schedule, four nonreinforced trials preceded a reinforced trial each day, and under the R4N schedule, a reinforced trial was followed by four nonreinforced trials each day. The major finding obtained was that under the 4NR schedule, discriminative responding was improved very substantially by a shift to extinction. Rats maintained on the 4NR schedule did not show improved discriminative responding, nor did discriminative responding improve in extinction following training under either the R4N schedule or a schedule of consistent reinforcement. Latent discrimination learning was defined as discriminative responding which fails to reflect adequately the amount of discrimination learning accomplished. The present findings demonstrate latent discrimination learning for regular schedules of partial reinforcement, something already demonstrated for brightness differential conditioning and possibly DRL schedules, as well.  相似文献   

15.
In three experiments, we examined the effect on the patterns of responding noted on fixed interval (FI) schedules of prior exposure to a range of interval and ratio schedules. Rats leverpressed for food reinforcement on random ratio (RR), random interval (RI), or variable interval (VI) schedules prior to transfer to FI schedules. In Experiment 1, prior exposure to an RR schedule retarded the development of typical FI patterns of responding. Exposure to a yoked RI schedule produced even greater retardation of typical FI performance. This effect was replicated in Experiment 2, using a within-subjects design. Rats responded on a multiple RR-RI schedule prior to a multiple FI-FI schedule. Typical FI performance emerged more slowly in the component previously associated with the RI than with that associated with the RR. In Experiment 3, exposure to an RR schedule retarded the development of FI performance to a greater extent than did exposure to a VR schedule. The latter schedule was programmed to allow the possibility that inhibitory control would develop after reinforcement. These results confirm that ratio schedules independently result in the disruption of FI responding. This effect was not long lasting and cannot be used plausibly to explain species differences in responding to FI schedules. However, it does suggest that temporal control—as manifested by the transfer of inhibitory control from one schedule to another—could facilitate movement between interval schedules.  相似文献   

16.
Four pigeons were exposed to multiple schedules with concurrent variable interval (VI) components and then tested for preference transfer. Half of the pigeons were trained on a multiple concurrent VI 20-sec, VI 40-sec/cuncurrent VI 4G-sec5 VI 80-sec schedule. The remaining pigeons were trained on a multiple concurrent VI 80-sec, VI 40-sec/concurrent VI 40-sec, VI 20-sec schedule-After stability criteria for time and response proportions were simultaneously met, four preference transfer tests were conducted with the stimuli associated with the VI 40-sec schedules. During the transfer tests, each pigeon allocated a greater proportion of responses (M=0,79) and time (M=0.82) to the stimulus associated with the VI 40-sec schedule that was paired with the VI 80-sec schedule than lo the VI 40-sec schedule stimulus paired with the VI 20-sec schedule. Absolute reinforcement rates on the two VI 40 sec schedules were approximately equal and unlikely to account for the observed preference. Nor was the preference consistent with the differences in local reinforcement rates associated with the two stimuli. Instead, the results were interpreted in terms of the differential value that stimuli acquire as a function of previous pairings with alternative schedules of reinforcement.  相似文献   

17.
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   

18.
Sated rats, previously trained to leverpress for H2O reinforcement on continuous or variable-interval (10-sec or 60-sec) schedules, were given NaCl injections and tested for leverpressing. Under all schedules, responding was an inverted U function of NaCl concentration (0.15M to 3.0M). However, NaCl thirst produced relatively little change in behavior under the VI 60-sec schedule.  相似文献   

19.
The effects of reinforcement rate on behavioral contrast were examined in pigeons and rats. Each species was exposed to a series of 12 multiple variable-interval schedules, divided into four 3-schedule series. Each series consisted of a standard contrast manipulation, and baseline schedules provided a different rate of reinforcement in each of the series. The functions relating reinforcement rate to the magnitude of contrast were different across species. Rats showed a U-shaped function, with reliable contrast occurring only at high reinforcement rates. Pigeons showed an inverted U-shaped function, with contrast occurring on all schedules except the schedule providing the lowest rate of reinforcement. Pigeons discriminated between schedule components better than rats did, although differences in discrimination were probably not responsible for the differences in contrast. The results suggest that behavioral contrast in rats may be a different phenomenon from behavioral contrast in pigeons. The results cannot be explained by current theories, which view contrast as the product of a single general process.  相似文献   

20.
Two accounts of how density of reinforcement affects steady-state performance on probabilistic schedules were compared: the real-time linear operator (RTLO) model and a temporal control model (in which response strength is determined by reinforcement probability as a function of postreinforcement time). In Experiment 1, the probability of reinforcement repeatedly cycled between extinction and a random-ratio 10 schedule. Response-rate gain and phase did not change with period of the cycle as predicted by the RTLO model, nor did either model predict the differences in response rate following reinforcement at different points in the cycle. In Experiment 2, the probability of reinforcement was elevated immediately following a reinforcement but fell after a few seconds. Previous reinforcements had no effect upon responding. An extension of the temporal control model, the cumulative impulse model, allowed for the summing of response strength over successive reinforcements and was consistent with the data of both experiments.  相似文献   

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