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1.
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   

2.
The effects of changeover delays of fixed or variable duration on concurrent variable-interval performance in pigeons were investigated in a series of three experiments. Experiment 1 compared the effects of a fixed, variable, or variable signaled changeover delay on interchangeover times and responding during and after the changeover delay. The duration of the changeover delays was systematically varied in Experiment 2, and the relative reinforcement frequencies were manipulated in Experiment 3. Interchangeover times were found to be shorter when changeover delays of variable duration were compared with those of fixed duration. Changeover delays of fixed duration produced higher response rates during the changeover delay than after the changeover delay had elapsed; changeover delays of variable duration produced such differences to a lesser extent. It was concluded that the changeover delay in concurrent variable-interval schedules of reinforcement functionally acts as a delay period to the next opportunity for reinforcement, possibly serving as a conditioned reinforcer for the behavior preceding it (the interchangeover time) and as a discriminative stimulus for the behavior in its presence (response rates during the delay).  相似文献   

3.
Pigeons were trained on a multiple schedule of reinforcement in which each component was a concurrent schedule. The concurrent schedules were programmed by the changeover-key procedure. The primary purpose was to determine if the relative behavior allocated to two response alternatives is affected when absolute changes in these behaviors occur; i.e., to determine if matching is affected when positive behavioral contrast occurs. Results showed that (1) relative behavior in the unaltered component of the multiple schedule is not disrupted when positive contrast occurs in that component, (2) positive contrast occurred when the overall frequency of reinforcement in the reinforcement-correlated component(s) was high, but not when it was low, (3) changeover behavior was susceptible to positive contrast effects, and (4) changeover contrast and food-key contrast are independent phenomena.  相似文献   

4.
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   

5.
Pigeons responded to changeover-key concurrent variable-interval variable-interval reinforcement schedules while there were intervals during which the changeover key was inoperative (no-choice intervals). In Experiment 1, a multiple schedule on the changeover key signaled choice and no-choice intervals. All subjects showed near-perfect discrimination during initial discrimination training and rapid reacquisition of discrimination following contingency reversals. In Experiment 2, the onset of no-choice intervals was unsignaled and contingent on interchangeover time. The temporal distribution of changeover-key responses conformed to the temporal distribution of choice intervals. The results of both experiments suggest that changeover responding is modifiable as a function of its immediate consequences. The results of Experiment 2, in particular, suggest that time or some correlate of time since the last changeover response can determine subsequent changeover behavior.  相似文献   

6.
In the first condition in Experiment 1, 6 rats were exposed to concurrent variable ratio (VR) 30, variable interval (VI) 30-sec schedules. In the next two conditions, the subjects were exposed to concurrent VI VI schedules and concurrent tandem VI-differential-reinforcement-of-high-rate VI schedules. For the latter conditions, the overall and relative reinforcer rates equaled those in the first condition. Only minor differences appeared in time allocation (a molar measure) across conditions. However, local response rate differences (a molecular measure) appeared between schedule types consistently with the interresponse times these schedules reinforced. In Experiment 2, these findings reappeared when the prior experiment was replicated with 5 subjects, except that the VR schedule was replaced by a VI plus linear feedback schedule. These results suggest that within the context tested, the molar factor of relative reinforcement rate controls preference, whereas the molecular factor of the relation between interresponse times and reinforcer probability controls the local response rate.  相似文献   

7.
The aim of the four present experiments was to explore how different schedules of reinforcement influence schedule-induced behavior, their impact on evaluative ratings given to conditioned stimuli associated with each schedule through evaluative conditioning, and the transfer of these evaluations through derived stimulus networks. Experiment 1 compared two contrasting response reinforcement rules (variable ratio [VR], variable interval [VI]). Experiment 2 varied the response to reinforcement rule between two schedules but equated the outcome to response rate (differential reinforcement of high rate [DRH] vs. VR). Experiment 3 compared molar and molecular aspects of contingencies of reinforcement (tandem VIVR vs. tandem VRVI). Finally, Experiment 4 employed schedules that induced low rates of responding to determine whether, under these circumstances, responses were more sensitive to the molecular aspects of a schedule (differential reinforcement of low rate [DRL] vs. VI). The findings suggest that the transfer of evaluative functions is determined mainly by differences in response rate between the schedules and the molar aspects of the schedules. However, when neither schedule was based on a strong response reinforcement rule, the transfer of evaluative judgments came under the control of the molecular aspects of the schedule.  相似文献   

8.
Four pigeons were exposed to several nonindependent concurrent variable-interval schedules of reinforcement. One schedule component required a keypecking response; the other component required a treadlepressing response. The birds matched the ratio of their behavior (as measured by responses and time) between the two topographically different responses to the ratio of reinforcement in those two components. When additional foods not contingent on a keypeck or treadle-press were then added, the birds matched time spent in the components to total rates of food delivered in those components; response matching was somewhat disrupted. The matching law, developed under concurrent variable-interval schedules requiring similar responses, can thus account for choice behavior involving topographically different responses.  相似文献   

9.
Pigeons responded to concurrent variable-interval variable-interval schedules of food reinforcement. Interchangeover times and reinforcements were recorded in intact time series during acquisition following several schedule-density manipulations. Probability of a changeover, while constant as a function of time since the previous changeover, was found to be a nonmonotonically increasing function of time since reinforcement. Autocorrelation analyses of intact time series revealed the presence of statistically significant sequential dependencies in the time series during acquisition, but not during asymptotic performance. Lag transformations of actual interchangeover times revealed inhomogeneities in the time series not shown in the autocorrelations or in the overall distribution of interchangeover times.  相似文献   

10.
Separate groups of food- and water-deprived rats pressed a lever for food or water, respectively, on continuous reinforcement and various fixed-ratio and fixed-interval reinforcement schedules. Food-reinforced rats on continuous, FR 2-, or FI 10-sec schedules showed consistently longer mean lever contact durations per leverpress than did water-reinforced rats on the same schedules. Mean lever-contact-duration differences between food- and water-reinforced rats were greatly attenuated or disappeared under FR 4-, FR 8-, FI 20-sec, and FI 30-sec schedules of reinforcement. These results are interpreted as supporting earlier hypotheses that there are respondent components of operantly conditioned and autoshaped leverpresses, but that these respondent components weaken with partial reinforcement and the leverpress topography comes under the control of operant contingencies.  相似文献   

11.
Pigeons were trained on a multiple schedule in which separate concurrent schedules were presented in the two components of the schedule. During one component, concurrent variable-interval 40-sec variableinterval 80-sec schedules operated. In the second component, concurrent variable-interval 40-sec variableinterval 20-sec schedules operated. After stable baseline performance was obtained in both components, extinction probe choice tests were presented to assess preference between the variable-interval 40-sec schedules from the two components. The variable-interval 40-sec schedule paired with the variableinterval 80-sec schedule was preferred over the variable-interval 40-sec schedule paired with the variableinterval 20-sec schedule. The subjects were also exposed to several resistance-to-change manipulations: (1) prefeeding prior to the experimental session, (2) a free-food schedule added to timeout periods separating components, and (3) extinction. The results indicated that preference and resistance to change do not necessarily covary.  相似文献   

12.
How do animals choose between opportunities to run of different durations? Are longer durations preferred over shorter durations because they permit a greater number of revolutions? Are shorter durations preferred because they engender higher rates of running? Will longer durations be chosen because running is less constrained? The present study reports on three experiments that attempted to address these questions. In the first experiment, five male Wistar rats chose between 10-sec and 50-sec opportunities to run on modified concurrent variable-interval (VI) schedules. Across conditions, the durations associated with the alternatives were reversed. Response, time, and reinforcer proportions did not vary from indifference. In a second experiment, eight female Long-Evans rats chose between opportunities to run of equal (30 sec) and unequal durations (10 sec and 50 sec) on concurrent variable-ratio (VR) schedules. As in Experiment 1, between presentations of equal duration conditions, 10-sec and 50-sec durations were reversed. Results showed that response, time, and reinforcer proportions on an alternative did not vary with reinforcer duration. In a third experiment, using concurrent VR schedules, durations were systematically varied to decrease the shorter duration toward 0 sec. As the shorter duration decreased, response, time, and reinforcer proportions shifted toward the longer duration. In summary, differences in durations of opportunities to run did not affect choice behavior in a manner consistent with the assumption that a longer reinforcer is a larger reinforcer.  相似文献   

13.
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   

14.
Pigeons were trained on multiple schedules with component stimuli of different degrees of similarity. In Experiment 1, a two-component schedule was used in which the two stimuli were either two line orientations or a line orientation versus a diffuse color. Reinforcement rate was varied in one component to determine the effects of stimulus similarity on different aspects of behavioral contrast. Contrast in terms of average response rates (molar contrast) was larger with less similar stimuli. Local contrast effects at the beginning of the component were larger for more similar stimuli, but these effects were more variable and did not attain statistical significance. Independent of the level of molar contrast, the local pattern of schedule interaction differed for the two levels of similarity: with more similar stimuli, the maximum degree of interaction occurred at the beginning of the components and then decreased; with less similar stimuli, the degree of interaction increased throughout the components and was at its maximum near their end. In Experiment 2, the same three stimuli were used while reinforcement rate in the middle component of a three-component sequence was varied; this isolated the effects of the preceding schedule from those of the following schedule. Contrast effects were generally greater in the target component preceding the variable schedule, and these were enhanced by less similar stimuli. Contrast in the target component following the variable schedule was manifested primarily in terms of the behavior at the beginning of the component, and these effects were inconsistently related to stimulus similarity. The functional separation of the effects of stimulus similarity on the different locations of contrast suggest that “anticipatory contrast” and “local contrast” depend upon different mechanisms, thus excluding any account of contrast solely in terms of relative rate of reinforcement.  相似文献   

15.
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   

16.
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   

17.
Two experiments are reported in which, by pressing a lever, unsignaled avoidable shocks could be changed to signaled avoidable shocks for periods of 1 min, after which unsignaled avoidance was automatically reinstated. A correlated stimulus identified the signaled schedule. Under these conditions, Ss changed over at a rate sufficient to remain in the signaled schedule more than 90% of the time. Both experiments showed that changeover performance was under the control of the correlated stimulus. Presenting the signaled schedule without the correlated stimulus did not maintain changing over. The second experiment showed that a 1-sec presentation of the correlated stimulus was sufficient to maintain changeover performance. The results were attributed to the conditioned reinforcing properties of the correlated stimulus.  相似文献   

18.
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   

19.
When pigeons are required to peck each of two keys in any order for reinforcement, stereotyped response sequences develop that are resistant to disruption by extinction, schedules of reinforcement, or contingencies requiring sequence variability. To test the hypothesis that stereotyped response sequences become integrated behavioral units, two experiments introduced within-sequence temporal delays of varying duration. Experiment 1 found that when a delay followed each peck in a sequence, there was substantial disruption of sequence performance that was independent of delay duration. However, such disruption was only temporary. Experiment 2 found that when the location of a delay within a sequence was varied, sequence disruption was a function of when, in a sequence, the delay occurred. Delays that occurred within sequence subunits had large effects, whereas delays that occurred between such subunits had small effects. The data indicate that pigeons can learn to bridge within-sequence delays, and suggest that response sequences are organized into “phrases.”  相似文献   

20.
Experiment 1 investigated the behavior of rats trained to leverpress on a concurrent variable ratio (VR) 30 VR-30 schedule with a brief, 500-msec, light occurring at the midpoint of the ratio on one of the levers. Higher response rates were recorded on the lever associated with this stimulus, a finding that paralleled the effect produced by inserting primary reinforcement at the midpoint (i.e., by training on a concurrent VR-30 VR-15 schedule). Similar results were found in Experiment 2 using a concurrent VR-20 VR-20 schedule with a 2-sec visual stimulus presented midway through one of the components. In addition, a brief stimulus inserted midway through the VR-20 component of a concurrent VR-20 VR-10 schedule retarded the development of a difference in response rates between the components relative to a VR-20 VR-10 group lacking the signal. In Experiment 3, multiple VR VR schedules were used. Again, the response rate was higher in the component that had the added stimulus or, for a second group of subjects, on the component with the smaller response requirement. Probe-choice trials revealed a preference for the component that generated the higher rate in both groups. Presenting a stimulus partway through a ratio appears to reduce the effect on response rate and choice of a large ratio value.  相似文献   

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