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.     

Effects of methamphetamine and scopolamine on variability of response location.

Methamphetamine and scopolamine were studied in monkeys responding under a multiple fixed-ratio fixed-interval schedule of reinforcement. A response on any one of six levers could satisfy the schedule requirements. Variability of response location was evaluated in terms of switches, where a switch was defined as a response on one lever followed by a response on a different lever. Under baseline conditions the fixed-ratio schedule generated a high rate of responding and a low level of variability, while the fixed-interval schedule generated a low rate of responding and a high level of variability. Both methamphetamine (0.1 to 0.5 mg/kg) and scopolamine (2.4 to 240 microgram/kg) decreased overall response rate and increased variability of response location in each component of the multiple schedule with increasing doses of drug. At lower doses both drugs were found to decrease rate without affecting response variability.     

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.     

Logit models and logistic regressions for social networks: III. Valued relations

This paper generalizes thep* model for dichotomous social network data (Wasserman & Pattison, 1996) to the polytomous case. The generalization is achieved by transforming valued social networks into three-way binary arrays. This data transformation requires a modification of the Hammersley-Clifford theorem that underpins thep* class of models. We demonstrate that, provided that certain (non-observed) data patterns are excluded from consideration, a suitable version of the theorem can be developed. We also show that the approach amounts to a model for multiple logits derived from a pseudo-likelihood function. Estimation within this model is analogous to the separate fitting of multinomial baseline logits, except that the Hammersley-Clifford theorem requires the equating of certain parameters across logits. The paper describes how to convert a valued network into a data array suitable for fitting the model and provides some illustrative empirical examples.This research was supported by grants from the Australian Research Council, the National Science Foundation (#SBR96-30754), and the National Institute of Health (#PHS-1RO1-39829-01).     

The behavioral theory of timing: Reinforcer rate determines pacemaker rate

In the behavioral theory of timing, pulses from a hypothetical Poisson pacemaker produce transitions between states that are correlated with adjunctive behavior. The adjunctive behavior serves as a discriminative stimulus for temporal discriminations. The present experiments tested the assumption that the average interpulse time of the pacemaker is proportional to interreinforcer interval. Responses on a left key were reinforced at variable intervals for the first 25 s since the beginning of a 50-s trial, and right-key responses were reinforced at variable intervals during the second 25 s. Psychometric functions relating proportion of right-key responses to time since trial onset, in 5-s intervals across the 50-s trial, were sigmoidal in form. Average interpulse times derived by fitting quantitative predictions from the behavioral theory of timing to obtained psychometric functions decreased when the interreinforcer interval was decreased and increased when the interreinforcer interval was increased, as predicted by the theory. In a second experiment, average interpulse times estimated from trials without reinforcement followed global changes in interreinforcer interval, as predicted by the theory. Changes in temporal discrimination as a function of interreinforcer interval were therefore not influenced by the discrimination of reinforcer occurrence. The present data support the assumption of the behavioral theory of timing that interpulse time is determined by interreinforcer interval.     

Some critical observations of the test information function as a measure of local accuracy in ability estimation

The test information function serves important roles in latent trait models and in their applications. Among others, it has been used as the measure of accuracy in ability estimation. A question arises, however, if the test information function is accurate enough for all meaningful levels of ability relative to the test, especially when the number of test items is relatively small (e.g., less than 50). In the present paper, using the constant information model and constant amounts of test information for a finite interval of ability, simulated data were produced for eight different levels of ability and for twenty different numbers of test items ranging between 10 and 200. Analyses of these data suggest that it is desirable to consider some modification of the test information function when it is used as the measure of accuracy in ability estimation.     

Performances on ratio and interval schedules of reinforcement: Data and theory

Two differences between ratio and interval performance are well known: (a) Higher rates occur on ratio schedules, and (b) ratio schedules are unable to maintain responding at low rates of reinforcement (ratio “strain”). A third phenomenon, a downturn in response rate at the highest rates of reinforcement, is well documented for ratio schedules and is predicted for interval schedules. Pigeons were exposed to multiple variable-ratio variable-interval schedules in which the intervals generated in the variable-ratio component were programmed in the variable-interval component, thereby “yoking” or approximately matching reinforcement in the two components. The full range of ratio performances was studied, from strained to continuous reinforcement. In addition to the expected phenomena, a new phenomenon was observed: an upturn in variable-interval response rate in the midrange of rates of reinforcement that brought response rates on the two schedules to equality before the downturn at the highest rates of reinforcement. When the average response rate was corrected by eliminating pausing after reinforcement, the downturn in response rate vanished, leaving a strictly monotonic performance curve. This apparent functional independence of the postreinforcement pause and the qualitative shift in response implied by the upturn in variable-interval response rate suggest that theoretical accounts will require thinking of behavior as partitioned among at least three categories, and probably four: postreinforcement activity, other unprogrammed activity, ratio-typical operant behavior, and interval-typical operant behavior.     

企业三类人员对人际关系及知识分子重要性的估计

本文探讨了企业不同层次的领导人与技术人员对有关企业领导人与知识分子的人际关系、知识分子的重要性及其发挥作用的程度等问题的评价差异。研究表明,他们在下述二方面的主观评价上存在着显著的差异:(1)企业领导人与知识分子之间的人际关系;(2)知识分子的重要性。文章也谈了作者关于这类主观评价差异研究的一些思考。     

Performance of children under a multiple random-ratio random-interval schedule of reinforcement

Three children, aged 1.5, 2.5, and 4.5 years, pressed telegraph keys under a two-component multiple random-ratio random-interval schedule of reinforcement. In the first condition, responses on the left key were reinforced under a random-interval schedule and responses on the right key were reinforced under a random-ratio schedule. In the second condition, the schedule components were reversed. In the third condition, the original arrangement was reinstated. For all subjects, rates of responding were higher in the random-ratio component despite higher rates of reinforcement in the random-interval component. The average interreinforcement interval of the random-interval component was increased in the fourth condition, resulting in more similar rates of reinforcement for both schedule components, and then returned to its original value in the fifth condition. In both conditions, all subjects continued to exhibit higher rates of responding in the ratio component than in the interval component. Although these observations are consistent with results from studies with pigeons, it is argued that the response-rate differences between the interval and ratio schedule components are sufficient to demonstrate schedule sensitivity.