Concurrent second-order schedules of reinforcement

Responses on one key (the main key) of a two-key chamber produced food according to a second-order variable-interval schedule with fixed-interval schedule components. A response on a second key (the changeover key) alternated colors on the main key and provided a second independent second-order variable-interval schedule with fixed-interval components. The fixed-interval component on one variable-interval schedule was held constant at 8 sec, while the fixed interval on the other variable-interval schedule was varied from 0 to 32 sec. Under some conditions, a brief stimulus terminated each fixed interval and generated fixed-interval patterns; in other conditions, the brief stimulus was omitted. Relative response rate and relative time deviated substantially from scheduled relative reinforcement rate and, to a lesser extent, from obtained relative reinforcement rate under both brief-stimulus and no-stimulus conditions. Matching was observed with equal components on both schedules; with unequal components, increasingly greater proportions of time and responses than the matching relation would predict were spent on the variable-interval schedule containing the shorter component. Preference for the shorter fixed interval was typically more extreme under brief-stimulus than under no-stimulus schedules. The results limit the extension of the matching relation typically observed under simple concurrent variable-interval schedules to concurrent second-order variable-interval schedules.     

The economics of daily consumption controlling food- and water-reinforced responding

In the first experiment, two rhesus monkeys earned their entire ration of food and water during daily sessions with no provisions to ensure constant daily intakes. Two variable-interval schedules of food presentations were concurrent with one variable-interval schedule of water presentations; the maximum rate of food presentations arranged by one food schedule was varied. As the rate of food presentations was increased, the absolute level of responding on the two food schedules combined decreased, while responding on the water schedule increased. The preference for the variable food schedule compared to the other food schedule approximately matched the proportion of reinforcers obtained from it. The preference for the variable food schedule compared to the water schedule did not match, but greatly decreased, as the proportion of reinforcers from the food schedule increased. When Experiment I was replicated, with provisions to ensure constant daily intakes of food and water (Experiment II), the absolute response rates under the two food schedules combined and under the water schedule no longer changed with increases in the rate of food during the sessions. On the other hand, choice between the two food schedules remained proportional to the distribution of obtained food pellets. These results were interpreted as indicating that behavior to obtain nonsubstitutable commodities, such as food and water, is strongly controlled by the economic conditions of daily consumption, while choice between substitutable commodities is independent of these factors.     

PDP启动型实验程序与Richardson-Klavehn模型的比较研究

2个实验对PDP的启动型实验程序与Richardson-Klavehn的修正模型进行了比较研究,通过对指示语的操纵,考察提取策略是否完全受意志控制,以及注意水平、刺激材料、测验类型、加工水平对被试作业的影响.结果发现刺激材料对有意识控制记忆的实验结果影响很大,对PDP的无意识自动加工参数无影响;启动型实验程序的结果与PDP理论相当一致;提取策略不一定是受意志精确控制的.     

A feature-integration theory of attention

A new hypothesis about the role of focused attention is proposed. The feature-integration theory of attention suggests that attention must be directed serially to each stimulus in a display whenever conjunctions of more than one separable feature are needed to characterize or distinguish the possible objects presented. A number of predictions were tested in a variety of paradigms including visual search, texture segregation, identification and localization, and using both separable dimensions (shape and color) and local elements or parts of figures (lines, curves, etc. in letters) as the features to be integrated into complex wholes. The results were in general consistent with the hypothesis. They offer a new set of criteria for distinguishing separable from integral features and a new rationale for predicting which tasks will show attention limits and which will not.     

Asymmetric attributions for compliance: Reward vs punishment

It was proposed that people attribute an individual's behavior more to internal factors when that individual's actions are influenced by reward than when those actions are influenced by punishment. Previous research has failed to control for the power of reward versus punishment which, in effect, creates a confounding of behavioral base rates (consensus) with the reward-punishment manipulation. The current research created reward and punishment contingencies that were equal in their base rates for producing a compliant response. In Experiment 1, subjects (n = 63) who produced the base-rate data also made attributions regarding a compliant target person. The results supported the reward-punishment attributional asymmetry hypothesis in that the target person was held more responsible for his actions in the reward than in the punishment conditions. A second experiment (n = 72) provided some attributors with information regarding base rates for compliance and measured perceived base rates for compliance. Knowledge of the base rates for compliance eliminated the reward-punishment attributional asymmetry phenomenon. Subjects not provided with such knowledge erroneously assumed different base rates for reward and punishment and maintained the perception of reward-punishment attributional asymmetry. Using subjects' estimates of base rate for compliance as a covariate eliminated the attributional asymmetry effect. It is suggested that erroneous base-rate assumptions mediate the attributional asymmetry phenomenon.     

Alleys in visual space

Geometry of frameless visual space is dealt with. First, parallel and equidistant alleys, horopters in the horizontal plane of eyes' level are discussed within the framework of the Luneburg's model that the frameless visual space is a Riemannian space of constant curvature. That basic postulate and the specific mapping functions assumed by Luneburg between the euclidean map of visual space and the physical space are kept separate, and efforts are directed to make the model applicable to more natural conditions of our visual space. A possibility is pointed out to remove the constraint “frameless” in the sense that perceptual geometrical properties are primarily determined by the convergence of optic axes. So far, only alleys in the horizontal plane extending from us toward infinity have been studied, but more often we perceive parallel lines, horizontal or vertical, in front of us like shelves of a bookcase. Hence, equations are derived for horopter plane appearing fronto-parallel in the three-dimensional visual space and alleys running horizontally or vertically on the horopter plane. It is shown that parallel and equidistant alleys are not the same in the horopter plane as in the horizontal plane, if the visual space is not euclidean. A method to evaluate the discrepancy between the two alleys without using any mapping functions is stated with some numerical examples.     

An experimental analysis of the effects of d-amphetamine and cocaine on the acquisition and performance of response chains in monkeys.

In one component of a multiple schedule of food presentation, monkeys acquired a different four-response chain each session by responding sequentially on three keys in the presence of four geometric forms (learning). In the other component, the four-response chain was the same each session (performance). Both d-amphetamine and cocaine, at the higher doses, disrupted the behavior in the learning component; the overall response rate decreased, the overall accuracy was impaired (i.e., percent errors increased), and there was less within-session error reduction. The performance component was generally less sensitive than the learning component to the disruptive effects of both drugs on rate and accuracy. After pre-feeding or during an extended session, the response rate decreased in both components, but accuracy was generally unaffected. When the four discriminative stimuli in both components were removed, the behavior was disrupted to a greater extent in the performance component. The disruptive effects of both drugs on behavior in the learning component were attenuated when the drugs were administered during the session after the response chain had been acquired. It was concluded that the greater sensitivity of the learning component to disruptive drug effects is related to the relatively weak stimulus control and/or the lower rate of reinforcement associated with that component.     

Concurrent-schedule performance: Effects of relative and overall reinforcer rate

Six pigeons were trained to respond on two keys, each of which provided reinforcers on an arithmetic variable-interval schedule. These concurrent schedules ran nonindependently with a 2-s changeover delay. Six sets of conditions were conducted. Within each set of conditions the ratio of reinforcers available on the two alternatives was varied, but the arranged overall reinforcer rate remained constant. Each set of conditions used a different overall reinforcer rate, ranging from 0.22 reinforcers per minute to 10 reinforcers per minute. The generalized matching law fit the data from each set of conditions, but sensitivity to reinforcer frequency (a) decreased as the overall reinforcer rate decreased for both time allocation and response allocation based analyses of the data. Overall response rates did not vary with changes in relative reinforcer rate, but decreased with decreases in overall reinforcer rate. Changeover rates varied as a function of both relative and overall reinforcer rates. However, as explanations based on changeover rate seem unable to deal with the changes in generalized matching sensitivity, discrimination accounts of choice may offer a more promising interpretation.     

Variable-interval schedules of timeout from avoidance

Rats were trained on concurrent schedules in which pressing one lever postponed shock and pressing the other occasionally produced a 2-min timeout during which the shock-postponement schedule was suspended and its correlated stimuli were removed. Throughout, the shock-postponement schedule maintained proficient levels of avoidance. Nevertheless, in Experiment 1 responding on the timeout lever was established rapidly, was maintained at stable levels on variable-interval schedules, was extinguished by withholding timeout, was reestablished when timeout was reintroduced, and was brought under discriminative control with a multiple variable-interval extinction schedule of timeout. These results are in contrast with Verhave's (1962) conclusion that timeout is an ineffective reinforcer when presented to rats on intermittent schedules. In Experiment 2 the consequence of responding on the timeout lever was altered so that the shock-postponement schedule remained in effect even though the stimulus conditions associated with timeout were produced for 2 min. Responding extinguished, indicating that suspension of the shock-postponement schedule, not stimulus change, was the source of reinforcement. By establishing the reinforcing efficacy of timeout with standard variable-interval schedules, these experiments illustrate a procedure for studying negative reinforcement in the same way as positive reinforcement.     

Competitive fixed-interval performance in humans

Two persons responded in the same session in separate cubicles, but under a single schedule of reinforcement. Each time reinforcement was programmed, only the first response to occur, that is, the response of only one of the subjects, was reinforced. “Competitive” behavior that developed under these conditions was examined in three experiments. In Experiment 1 subjects responded under fixed-interval (FI) 30-s, 60-s, and 90-s schedules of reinforcement. Under the competition condition, relative to baseline conditions, the response rates were higher and the pattern was “break-and-run.” In Experiment 2, subjects were exposed first to a conventional FI schedule and then to an FI competition schedule. Next, they were trained to respond under either a differential-reinforcement-of-low-rate (DRL) or fixed-ratio (FR) schedule, and finally, the initial FI competition condition was reinstated. In this second exposure to the FI competition procedure, DRL subjects responded at lower rates than were emitted during the initial exposure to that condition and FR subjects responded at higher rates. For all subjects, however, responding gradually returned to the break-and-run pattern that had occurred during the first FI competition condition. Experiment 3 assessed potential variables contributing to the effects of the competitive FI contingencies during Experiments 1 and 2. Subjects were exposed to FI schedules where (a) probability of reinforcement at completion of each fixed interval was varied, or (b) a limited hold was in effect for reinforcement. Only under the limited hold was responding similar to that observed in previous experiments.