Some Effects Of Intertrial Interval Duration On Discrete-trial Choice

Pigeons were trained in Experiment 1 on a discrete-trial concurrent variable-interval (VI) 1-min VI 3-min schedule, and in Experiment 2 on a discrete-trial concurrent VI 1.5-min VI 1.5-min schedule. In each experiment, the intertrial-interval durations (ITIs) were 0 s, 6 s, 22 s, and 120 s, and the schedules were both independent and interdependent. The purpose of the research was to determine whether lengthening the ITI would disrupt any local control that existed, measured with respect to relative response rate and changeover probability. In Experiment 1, with the independent schedules, both preference and obtained relative reinforcement rate approximated .75 at short ITIs, but then decreased toward .50 with longer ITIs. With interdependent schedules, both preference and obtained relative reinforcement rate approximated .75 at all ITIs. In both experiments, with both independent and interdependent schedules, changeover probabilities for each response in a sequence of up to five successive responses to a given schedule were variable for individual birds. The average changeover probabilities for all birds suggested perseveration rather than a systematic increase within a given ITI or a systematic trend toward chance responding as ITI duration increased. Finally, the changeover functions did not differ when a sequence of responses was calculated to begin anew after reinforcement rather than with the first response on a schedule. Taken together, the data were inconsistent with a theory holding that only local processes underlie choice in discrete-trial procedures.     

Optimality And Concurrent Variable-interval Variable-ratio Schedules

Despite claims to the contrary, all leading theories about operant choice may be seen as models of optimality. Although melioration is often contrasted with global maximization, both make the same core assumptions as other versions of optimality theory, including momentary maximizing, hill climbing, and the various versions of optimal foraging theory. The present experiment aimed to test melioration against more global optimality and to apply the visit-by-visit analysis suggested by foraging theory. Rats were exposed to concurrent schedules in which one alternative was always variable-ratio 10 and the other alternative was a variable-interval schedule. Although choice relations varied from rat to rat, the overall results roughly confirmed the matching law, a result often taken to support melioration. Pooling the data across sessions and across rats, however, resulted in no increment in unsystematic variance, lending support to the contention by Ziriax and Silberberg (1984) that the choice relation is partly constrained. When the data were analyzed at the level of visits, the results either disconfirmed predictions of melioration or showed regularities about which melioration is silent. Instead, performance tended toward a rough optimization, in which responding favored the variable ratio, but with relatively brief visits to the variable interval. There were no asymmetries in travel or variability that would indicate that different processes were involved in generating visits at the two different schedules. The findings point toward a more global optimality model than melioration and demonstrate the value of per-visit analysis in the study of concurrent performances.     

Tail-measurability in monotone latent variable models

We consider latent variable models for an infinite sequence (or universe) of manifest (observable) variables that may be discrete, continuous or some combination of these. The main theorem is a general characterization by empirical conditions of when it is possible to construct latent variable models that satisfy unidimensionality, monotonicity, conditional independence, andtail-measurability. Tail-measurability means that the latent variable can be estimated consistently from the sequence of manifest variables even though an arbitrary finite subsequence has been removed. The characterizing,necessary and sufficient, conditions that the manifest variables must satisfy for these models are conditional association and vanishing conditional dependence (as one conditions upon successively more other manifest variables). Our main theorem considerably generalizes and sharpens earlier results of Ellis and van den Wollenberg (1993), Holland and Rosenbaum (1986), and Junker (1993). It is also related to the work of Stout (1990).The main theorem is preceded by many results for latent variable modelsin general—not necessarily unidimensional and monotone. They pertain to the uniqueness of latent variables and are connected with the conditional independence theorem of Suppes and Zanotti (1981). We discuss new definitions of the concepts of true-score and subpopulation, which generalize these notions from the stochastic subject, random sampling, and domain sampling formulations of latent variable models (e.g., Holland, 1990; Lord & Novick, 1968). These definitions do not require the a priori specification of a latent variable model.The authors made equivalent contributions to the results of this article. Ellis' research was supported by the Dutch Interuniversitary Graduate School of Psychometrics and Sociometrics. Junker's research was supported by ONR Grant N00014-87-K-0277, NIMH Grant MH15758, and a Carnegie Mellon University Faculty Development Grant. In addition Junker would like to acknowledge the hospitality of the Nijmegen Institute for Cognition and Information during his visit to the University of Nijmegen in August 5–10, 1993.     

The effect of punishment on free-operant choice behavior in humans

During Phase I, three female human subjects pressed a button for monetary reinforcement in five variable-interval schedules specifying different frequencies of reinforcement. On alternate days, responding was also punished (by subtracting money) according to a variable-ratio 34 schedule. In the absence of punishment, response rates conformed to Herrnstein's equation for single variable-interval schedules. Punishment suppressed responding at all frequencies of reinforcement. This was reflected in a change in the values of both constants in Herrnstein's equation: the value of the theoretical maximum response-rate parameter was reduced, and the parameter describing the reinforcement frequency corresponding to the half-maximal response rate was elevated. During Phase II, the same five schedules (A) were in operation (without punishment), but in addition, a concurrent variable-interval schedule (B) of standard reinforcement frequency was introduced. On alternate days, responding in Component B was punished according to a variable-ratio 34 schedule. In the absence of punishment, absolute response rates conformed to equations proposed by Herrnstein to describe performance in concurrent schedules; the ratios of the response rates in the two components and the ratios of the times spent in the two components conformed to the Matching Law. When responding in Component B was punished, response rates in Component B were reduced and those in Component A were elevated, these changes being reflected in distortions of the matching relationship.     

Relationship between response rate and reinforcement frequency in variable-interval schedules: the effect of the concentration of sucrose reinforcement

Four rats were exposed to variable-interval schedules specifying a range of different reinforcement frequencies, using sucrose of two different concentrations and distilled water as the reinforcer. With sucrose, the rates of responding of all four rats were increasing negatively accelerated functions of reinforcement frequency, the data conforming closely to Herrnstein's equation; this was also true of the data from three of the four rats when distilled water was used as the reinforcer. The values of both constants in Herrnstein's equation were related to the sucrose concentration: the asymptotic response rate decreased, and the reinforcement frequency corresponding to the half-maximal response rate increased, with decreasing sucrose concentration.     

Instrumental Values – Strong and Weak

What does it mean that an object has instrumental value? While some writers seem to think it means that the object bears a value, and that instrumental value accordingly is a kind of value, other writers seem to think that the object is not a value bearer but is only what is conducive to something of value. Contrary to what is the general view among philosophers of value, I argue that if instrumental value is a kind of value, then it is a kind of extrinsic final value.     

INTERRESPONSE TIME STRUCTURES IN VARIABLE-RATIO AND VARIABLE-INTERVAL SCHEDULES

The interresponse-time structures of pigeon key pecking were examined under variable-ratio, variable-interval, and variable-interval plus linear feedback schedules. Whereas the variable-ratio and variable-interval plus linear feedback schedules generally resulted in a distinct group of short interresponse times and a broad distribution of longer interresponse times, the variable-interval schedules generally showed a much more continuous distribution of interresponse times. The results were taken to indicate that a log survivor analysis or double exponential fit of interresponse times may not be universally applicable to the task of demonstrating that operant behavior can be dichotomized into bouts of engagement and periods of disengagement.     

心理咨询过程-效果研究现状及展望

心理咨询过程-效果研究考察咨询过程变量对咨询效果的影响。以人为中心流派、认知流派、行为流派、精神分析流派等都为该研究领域提供了理论基础。主要研究内容有咨询师的反应方式、会谈中的当事人行为、工作同盟、会谈中的重要内容等过程变量与效果的关系。该领域积累的成果还不多,这可能与过程-效果关系本身的复杂性有关,同时研究方法尚有许多欠缺,如考察复杂关系时使用的研究设计过于简单、测量工具不统一导致结果难以比较,有些测量工具不成熟信效度不高。未来的研究除了努力克服这些问题外,还应多考虑理论构建、内隐变量的调节和中介作用、当事人变量,在研究方法上应更为综合和多样化     

The reductive effects of noncontingent reinforcement fixed-time versus variable-time schedules.

The effects of fixed‐time (FT) and variable‐time (VT) schedules on responding were evaluated with 2 adults with mental retardation. Multielement and reversal designs were used to compare the effects of FT and VT schedules in reducing responses previously maintained on variable‐ratio reinforcement schedules. The schedules were equally effective in reducing the target behavior.     

时间期待的认知与神经机制

时间期待是指个体利用环境中的时间信息预测目标刺激何时出现的能力。相关的认知模型可以分为两类：一类侧重于解释时间期待的形成过程, 如痕迹条件反射模型、双加工模型、动态注意模型、时间定向理论等; 另一类侧重于解释时间期待的更新过程, 如策略模型和时间再定位模型等。不同类型的时间期待激活的脑区不同, 表明时间期待的产生和更新过程存在分离：期待的产生激活与运动有关的左侧脑区, 而期待的更新激活与控制有关的右侧脑区。