Reward Density And Variable-interval Schedule Performance In An Open Economy

There is no general agreement regarding the form of the relation between response rate and reinforcement rate when single schedules of reinforcement are studied in an open economy. The present study assessed the form of this relation using reward density, which incorporates both reinforcement rate and duration of access to food, as an independent variable. Reward density was manipulated with 4 pigeons by changing the value of the variable-interval schedule, the hopper duration, or both. The relations between response rate and reward density were sharply rising and hyperbolic in 3 of 4 pigeons, replicating results obtained by Catania and Reynolds (1968). Because eating efficiency was lower in conditions that provided longer hopper durations, programmed reward densities differed from obtained reward densities. When response rates were examined as a function of obtained reward densities, the same relations were demonstrated more strongly. In further clarifying the relation between response rate and reward density in an open economy, these results lend support to the conclusion that open and closed economies yield different behavioral effects.     

运动强度和持续时间对运动后过量氧耗的影响

本研究采用双因素实验设计探讨了运动负荷强度和持续时间对 E-POC的影响。实验结果发现 ,运动过程中机体净耗氧量主要取决于运动持续时间 ,而运动后的 EPOC既受运动强度 ,也受持续时间的影响 ,但以前者的作用更加明显 ;运动后 VO2 的恢复速度快于血乳酸的消除 ,不同运动条件下的氧亏量变化主要取决于运动负荷的强度。     

Associative interaction: joint control of key pecking by stimulus-reinforcer and response-reinforcer relationships

The joint control of rate of key pecking in pigeons by stimulus-reinforcer and response-reinforcer relationships was studied in the context of a two-component multiple schedule of reinforcement. Food presentation was always associated with one component and extinction with the other. The stimulus-reinforcer relationship was manipulated by varying the relative durations of the two components. In the food-presentation component, a fixed rate of reinforcement, independent of rate of responding, was generated by a schedule referred to as “T*”. One aspect of the response-reinforcer relationship, contiguity, was manipulated by varying the percentage of delayed reinforcers. With the multiple T* extinction schedule, stimulus-reinforcer and response-reinforcer relationships could be varied independently of one another. Rate of key pecking was sensitive to manipulations of both relationships. However, significant differential effects due to either the stimulus-reinforcer or response-reinforcer relationship were obtained only when the other relationship was weak: stimulus-reinforcer and response-reinforcer relationships interacted in the joint control of responding.     

The effects of component duration on multiple-schedule performance in closed and open economies.

Pigeons responded on multiple variable-interval variable-interval schedules of reinforcement in an open and a closed economy. Equal duration components were increased in duration while the component rates of reinforcement were held constant, the component schedules were reversed, and component duration was decreased. In the open economy, daily sessions were limited to 1 hr, and subjects were maintained at 80% of their free-feeding weights through supplemental feeding when necessary in their home cages. In the closed economy, subjects were housed in their experimental chambers and no deprivation regimen was enforced. Relative response rate decreased as components were lengthened in the open economy, whereas in the closed economy relative rate increased as components were lengthened. Response proportions overmatched reinforcer proportions to a greater extent at long component durations in the closed economy, but there was no systematic effect of component duration on responding in the open economy.     

Stimulus- and pellet-induced drinking during a successive discrimination

In three experiments, interim water drinking was examined in rats exposed to a multiple schedule whose two components were extinction and a variable-time 30-s schedule of food delivery. Two different drinking patterns were observed in Experiment 1. Pellet-induced drinking, characterized by high rates of postpellet drinking in the variable-time component, with little or no drinking in extinction, occurred when the acquisition of stable postpellet drinking preceded discrimination training. Stimulus-induced drinking, characterized by a burst of drinking at the onset of extinction, with no drinking during the variable-time schedule, occurred when discrimination training preceded all other experimental conditions. With extended training, stimulus-induced drinking eventually was accompanied by postpellet drinking. In Experiment 2, the rate of stimulus-induced drinking and the number of sessions during which it occurred without postpellet drinking were found to be inversely related to component duration. In Experiment 3, the rate of schedule-induced drinking was found to vary directly with component duration.     

Psychophysics of key-peck duration in the pigeon

The duration of the pigeon's key peck was differentially reinforced in either a trials or a free-operant procedure. Mean emitted peck duration was a power function of the duration required for food delivery to occur. The exponents of the power function differed considerably from those observed in earlier research involving longer duration responses in pigeons and other species. The coefficients of variation also did not correspond with those of the earlier research on other responses, nor did consideration of the durations actually reinforced resolve the differences. Duration was neither a function of response rate nor of intermittency of reinforcement. Key-peck duration was changed in an orderly way by differential reinforcement. However, it appeared to be more strongly determined by its duration in the absence of differential reinforcement than were longer duration responses.     

Multiple schedule component duration: a reanalysis of Shimp and Wheatley (1971) and Todorov (1972)

The tendency for relative response rate to approach matching as multiple schedule component duration decreases has been interpreted as confirming a prediction of Herrnstein's multiple schedule equation. However, the equation predicts that absolute response rate will decrease in both multiple schedule components as component duration decreases. The absolute response-rate data of two studies of component duration do not support this prediction; absolute rate either increased or remained relatively constant.     

Run length, visit duration, and reinforcers per visit in concurrent performance

The contingencies in each alternative of concurrent procedures consist of reinforcement for staying and reinforcement for switching. For the stay contingency, behavior directed at one alternative earns and obtains reinforcers. For the switch contingency, behavior directed at one alternative earns reinforcers but behavior directed at the other alternative obtains them. In Experiment 1, responses on the main lever, in S1, incremented stay and switch schedules and obtained a stay reinforcer when it became available. Responses on the switch lever changed S1 to S2 and obtained switch reinforcers when available. In S2, neither responses on the main lever nor on the switch lever were reinforced, but a switch response changed S2 to S1. Run lengths and visit durations were a function of the ratio of the scheduled probabilities of reinforcement (staying/switching). From run lengths and visit durations, traditional concurrent performance was synthesized, and that synthesized performance was consistent with the generalized matching law. Experiment 2 replicated and extended this analysis to concurrent variable-interval schedules. The synthesized results challenge any theory of matching that requires a comparison among the alternatives.     

Relative durations of conditioned stimulus and intertrial interval in conditioned suppression.

The effects of the relative durations of the conditional stimulus and the intertrial interval on bar pressing during a conditioned-suppression procedure were examined as a function of two additional variables--type of operant baseline schedule and rate of shock presentation. In Experiment 1, response suppression was compared across components of a multiple fixed-ratio, random-ratio, fixed-interval, random-interval schedule, at relative conditioned-stimulus/intertrial-interval durations of 1/1, 1/4, and 1/9. In Experiment 2, relative conditioned-stimulus/intertrial-interval duration (1/5, 3/3, or 5/1) was manipulated across groups, while shock frequency (2, 6, or 10 shocks/hr) was manipulated within groups. In both experiments, suppression during the signal was virtually complete at all relative durations. Responding was also suppressed during the intertrial interval, but that suppression varied as a function of experimental manipulations. In Experiment 1, intertrial-interval response rates were higher when relative signal duration was 1/9 than when it was 1/1, although both relative signal duration and shock frequency, which covaried, could have contributed to the difference. In Experiment 2, the patterning of response rates between successive shocks was affected by relative duration, absolute rates during the intertrial interval varied as a function of shock frequency, and differences between suppression during the signal and suppression during the intertrial interval were affected by both relative duration and shock frequency. The data support an analysis based upon relationships between shock-correlated and intertrial-interval stimuli and, as assessed by the relative-delay-to-reinforcement metric, are comparable to results that have been reported from experiments using similar manipulations under the autoshaping paradigm.     

不同情绪诱发方法有效性的比较研究

采用自我报告和生理反馈法,从强度、纯度、时间进程三方面考察图片、音乐、电影和回忆四种常用情绪诱发方法诱发出的高兴、激动、悲伤和恐惧四种不同维度的情绪的有效性。得出结论：（1）总体上,音乐诱发情绪的强度最高,图片最低;在积极情绪中,音乐诱发的强度普遍较高,图片较低;消极情绪中,回忆诱发的强度普遍较高,音乐较低。（2）音乐诱发情绪的纯度较高,图片较低。（3）效价和激活度不同,情绪的时间进程不同,高兴能持续将近1分钟,激动能持续2分30秒,悲伤能持续1分30秒,而恐惧能持续2分钟。