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1.
Three pigeons pecked keys for food reinforcers delivered by multiple variable interval variable interval schedules in the first part of each session (baseline) and by multiple variable interval extinction schedules in the second part of each session (contrast). The variable interval schedules delivered reinforcers after an average of 4 min or 30 sec in different conditions. The duration of a time-out between the components varied in five steps from 5 to 120 sec. Positive contrast occurred for all time-out durations in both experiments. That is, the rate of responding emitted during the constant, variable interval component was greater during the contrast than during the baseline schedules. The size of contrast did not change systematically with changes in timeout duration. These results violate most theories of contrast. They are compatible with the idea that animals integrate reinforcers over intervals longer than 2 min.  相似文献   

2.
Five pigeons pecked lighted keys for food reinforcers delivered by several multiple variable interval 2-min variable interval 2-min schedules. At different times, the components of the multiple schedule both supplied food reinforcers, both supplied water, or one supplied food and the other supplied water. Rates of responding during the water component of the food-water schedule were lower than the rates during comparable components of the water-water schedules (negative contrast). But, the rates of responding during the food component of the food-water schedule were not greater than the rates of responding during comparable components of the food-food schedules (absence of positive contrast) at two different levels of water deprivation. These results raise questions about several theories of behavioral contrast, and they may restrict the scope of any theory that attributes positive and negative contrast to symmetrical factors.  相似文献   

3.
Three experiments examined changes in size of multiple-schedule behavioral contrast with changes in an independent variable. Experiment 1 found that positive contrast generally increased with increases in component duration when pigeons pressed treadles. Experiments 2 and 3 found that positive and negative contrast generally increased with increases in the baseline rates of reinforcement when pigeons pecked keys. The experiments show that positive and negative contrast vary as similar functions of the same variables. Experiment 1 also suggests that these functions are different for different responses.  相似文献   

4.
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   

5.
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   

6.
Positive and negative behavioral contrast were examined when pigeons were required to keypeck in one component and treadle press in the other component of a series of multiple schedules. The experimental conditions were constructed so that the positive and negative contrast groups were exposed to complementary conditions. Positive keypeck and negative treadle-press contrast occurred in all subjects. Positive treadle-press contrast seemed to depend on the order of schedule presentation. Only one subject exhibited strong negative keypeck contrast. The results indicate that symmetrical conditions are not sufficient to produce positive and negative contrast for a given response when topographically different responses are used in the components of a multiple schedule. The results are globally consistent with the competition theory of behavioral contrast.  相似文献   

7.
Five pigeons pecked lighted keys for food reinforcers delivered by a multiple variable-time 30-sec variable-time 2-min schedule. The duration of the components varied from 5 sec to 16 min. The rate of responding generated by the more favorable component schedule decreased as component duration increased to an intermediate value and then increased with additional increases in duration. The decrease confirmed a prediction of additive theories of behavioral contrast. The rate of responding generated by the less favorable component did not increase as component duration increased. This decrease may represent a floor effect or it may violate a prediction of one additive theory of contrast.  相似文献   

8.
Homing pigeons were reinforced for emitting a perching response according to differential-reinforcement-of-low-rate (DRL) schedules. The spacing requirement between successive perchings was progressively increased by 1-sec steps up to 70 sec and then abruptly decreased to 60, 40, and 20 sec. IRT/OP (interresponse time/opportunity) functions were maximal near the time of reinforcement. The coefficients of variation of the IRT distributions (ratio between the interquartile range and median IRT) fluctuated around .32, testifying for equivalent levels of adjustment throughout the critical IRT range. The ratio between reinforced and total IRTs ranged between .90 and .20. These data contrast with the performance of another group of pigeons reinforced for a treadle-pressing response according to DRL schedules (flatter IRT/OP functions, high coefficients of variation, and low efficiencies). Despite these differences in temporal regulation between perching and treadle-pressing DRL, response rates and reinforcement rates followed the same trend in both cases: they decreased as schedule value increased. The DRL perching results are similar to previous results obtained in the same species when perching duration was reinforced.  相似文献   

9.
Previous research has demonstrated that running in a rotating wheel functions as a reinforcer for leverpressing in rats. In these studies, the pattern of responding was similar to the pattern of responding maintained by consummatory reinforcers, such as food and water. The present study investigated quantitative features of responding maintained by running. In previous experiments in which responses were reinforced according to variable-interval (VI) schedules and food and water served as the reinforcer, the equation for a rectangular hyperbola described the relationship between response rate and reinforcement rate. This experiment tested whether this quantitative regularity also applies to leverpressing maintained by the opportunity to run in a wheel. Fourteen male Wistar rats responded on levers for the opportunity to run. In each session, subjects were exposed to a series of VI schedules. An opportunity to run for 60 sec was the reinforcing consequence. Results showed that response rate was a negatively accelerated function of reinforcement rate, and the relationship between these two variables was described well by the equation for a rectangular hyperbola. To further test the similarity between running and consummatory reinforcers, the response requirement and access were manipulated. In previous experiments with food and water, these types of manipulations differentially changed the two parameters of the hyperbola. A similar pattern of results was obtained with wheel running. Thus, the equation appears to apply to running about as well as it does to consummatory reinforcers.  相似文献   

10.
11.
Salt-hungry rats fail to develop anticipatory wheel-running activity when maintained under schedules of limited daily access to salt, in marked contrast to the robust anticipatory activity seen under food-access schedules. This suggests that the circadian oscillator underlying food-anticipatory activity is specifically related to food access and does not readily generalize to other scheduled resources. However, an alternative hypothesis is that rats are capable of anticipating daily salt-access periods, but that this anticipation is not manifest in wheel-running activity. In the present study, we maintained adrenalectomized rats under schedules of limited daily access to salt in which all salt was obtained by leverpressing. The results indicate that rats are capable of anticipating daily salt access by reference to an endogenous circadian timing mechanism. However, this behavior differs in several respects from that seen under food-access schedules.  相似文献   

12.
Pigeons' keypecking was reinforced by food on baseline schedules of multiple variable interval (VI) x VI x and on contrast schedules of multiple VI x VI y. Deprivation of food was varied by maintaining subjects at 75%, 85%, and 95% (+/- 2%) of their free-feeding weights. Positive and negative behavioral contrast were observed. The size of the contrast was not systematically altered by changes in deprivation. Positive and negative contrast were both larger later in the session than they were earlier. Within-session decreases in responding were steeper for the baseline than for the contrast schedules for positive contrast. Within-session decreases were steeper for the contrast than for the baseline schedules for negative contrast. These results were predicted by the idea that different amounts of habituation to the reinforcer during the baseline and contrast schedules contribute to behavioral contrast. The results show that contrast occurs under conditions that reduce the effect of the following component. The results support the assumption that positive and negative contrast are produced by symmetrical theoretical variables.  相似文献   

13.
An experiment with pigeons related overall and local behavioral contrast to similarity between stimuli signaling multiple-schedule components. Similarity was defined both physically and by discrimination performance. Initial and final baseline conditions used two equal random-interval schedules. During two intervening test periods, the schedule accompanying one component was changed to extinction. In the first test, components alternated strictly; in the second test, random component sequences were used. Signaling wavelength stimuli were separated by 1.5, 2, or 14 nm. Overall positive contrast occurred reliably, but its amount depended neither on wavelength difference nor on discrimination performance. Local positive contrast was less frequently observed when signaling stimuli were physically dissimilar; however, the effect was most closely related to actual discrimination performance. The relationship between discrimination and local contrast was nonmonotonic, indicating maximum local contrast at intermediate discriminations.  相似文献   

14.
Two experiments tested the hypothesis that habituation contributes to within-session decreases in responding. In Experiment 1, rats’ leverpressing was reinforced under a fixed ratio (FR) 4 schedule throughout the baseline sessions. During the dishabituation sessions, the first 21 min and the last 21 min were FR 4; dishabituating events occurred during the middle 3 min. The dishabituating events altered the manner of reinforcer delivery in four different ways. Response rates increased after all dishabituating events. In Experiment 2, rats responded on several FR and variable ratio (VR) schedules. The ratio requirement varied from 3 to 15. Within-session decreases in responding were steeper during FR schedules than during VR schedules. In addition, response rates were well described as linear functions of cumulative number of food pellets eaten within sessions. These results support the habituation hypothesis but do not rule out the possibility that other satiety variables might contribute simultaneously.  相似文献   

15.
Response rate (responses per minute) and response duration (time in seconds per press) were recorded in rats shifted from multiple variable-interval variable-interval (mult VI VI) to multiple extinction variable-interval (mult EXT VI). This procedure produced positive contrast (i.e., a decrease in response rate in EXT and an increase in VI) in 11 of 12 rats and, in addition, produced an increase in response duration (i.e., bar holding), which, for the most part, was confined to the EXT component of the mult EXT VI condition. One of the 12 rats showed negative induction (i.e., a decrease in response rate in both the EXT and VI components), and also an increase in response duration in both the EXT and VI components of the mult EXT VI condition. The results indicate that generalization of behavior from the EXT to the VI component can produce negative induction, and that such generalization must be prevented if positive contrast is to occur in the rat.  相似文献   

16.
Groups of pigeons were exposed to multiple variable-interval variable-interval and multiple variable-interval extinction schedules of either food or water reinforcement for keypecking. Discriminative stimuli associated with component schedules were located either on the operant key or on a second “signal” key. When the stimuli were projected on the operant key, positive contrast appeared during discrimination conditions with either food or water as the reinforcer. When the stimuli were projected on the signal key, overall responding to the operant and signal keys showed contrast with food, but negative induction with water as the reinforcer. In the latter condition, the signal for the variable-interval shcedule of water reinforcement elicited a variety of water-related behavior, only some of which was directed at the signal. Thus, the type of reward and location of discriminative stimuli interacted to determine the presence or absence of behavioral contrast effects. In large part, these results support and extend the autoshaping view of contrast.  相似文献   

17.
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   

18.
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   

19.
We present an algebraic model of resistance to extinction that is consistent with research on resistance to change. The model assumes that response strength is a power function of reinforcer rate and that extinction involves two additive, decremental processes: (1) the termination of the reinforcement contingency and (2) generalization decrement resulting from reinforcer omission. The model was supported by three experiments. In Experiment 1, 4 pigeons were trained on two-component multiple variable-interval (VI) 60-sec, VI 240-sec schedules. In two conditions, resistance to change was tested by terminating the response-reinforcer contingency and presenting response-independent reinforcers at the same rate as in training. In two further conditions, resistance to change was tested by prefeeding and by extinction. In Experiment 2, 6 pigeons were trained on two-component multiple VI 150-sec schedules with 8-sec or 2-sec reinforcers, and resistance to change was tested by terminating the response-reinforcer contingency in three conditions. In two of those conditions, brief delays were interposed between responses and response-independent reinforcers. In both Experiments 1 and 2, response rate was more resistant to change in the richer component, except for extinction in Experiment 1. In Experiment 3, 8 pigeons were trained on multiple VI 30-sec, VI 120-sec schedules. During extinction, half of the presentations of each component were accompanied by a novel stimulus to produce generalization decrement. The extinction data of Experiments 1 and 3 were well described by our model. The value of the exponent relating response strength and reinforcement was similar in all three experiments.  相似文献   

20.
Three experiments delivered food at fixed or random intervals independently of the rat’s behavior, always less than the amount eaten with food freely available. The results revealed a Polydipsie response to this experimental suppression of eating, and total drinking decreased as total eating increased. When we added a lever that signaled each food delivery, leverpressing and drinking rose far above their baseline levels; both responses decreased as total eating increased. When a similar schedule presented lever and food independently, rats still became Polydipsie, but showed no sign of autoshaped leverpressing. A fourth experiment revealed a hypophagic response to schedules that suppressed drinking; total eating increased with total drinking. As mutual substitutes in the economic sense, one behavior falls as the other rises; as mutual complements in the economic sense, the two behaviors rise or fall together. We discuss polydipsia and autoshaping in terms of drinking as an intrinsic substitute for eating, and leverpressing as a learned substitute for eating. The results suggest a revision of conservation theory, which views drinking and eating as substitutes when the schedule suppresses eating but as complements when the schedule suppresses drinking.  相似文献   

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