Effects on preference of reinforcement delay, number of reinforcers, and terminal-link duration

Three experiments used concurrent-chains procedures to examine the effects of reinforcement delay, number of reinforcers, and terminal-link duration on preference. In Condition 30 of Experiment 1, food was delivered after 30 seconds in each 150-second terminal link, with four additional food deliveries occurring at 30-second intervals in one of the links. In Condition 5, food was delivered after 5 seconds in each 25-second terminal link, and the four additional reinforcers were delivered at 5-second intervals. Preferences for the multiple-food chain were greater in Condition 30. In Experiment 2, the terminal link(s) providing only one reinforcer terminated immediately after delivery of the reinforcer. Preferences for the multiple-food chain were smaller than in Experiment 1. In Condition 5 of Experiment 3, food was delivered after 5, 75, 100, 125, and 150 seconds in one 150-second link and after 5 seconds in the other. Condition 50 differed only in that the first (or only) reinforcer in each link was delivered after 50 seconds instead of after 5 seconds. Preferences for the multiple-food chain were greater in Condition 50. Results of Experiments 1 and 2 do not correspond to results obtained by Moore (1979).     

REPEATED ACQUISITION OF BEHAVIORAL CHAINS: RESPONSE SEQUENCES OR CONDITIONAL DISCRIMINATIONS?

The purpose of this study was to determine whether pigeons learn a sequence of positional responses or a series of conditional discriminations under a repeated-acquisition-of-behavioral-chains procedure. Three pigeons were trained under a repeated-acquisition procedure in which three different key colors served as stimuli correlated with the three steps in a chain. The order of presentation of the three stimuli was altered during the latter part of each test session after acquisition had occurred. If the pigeons had acquired a response sequence, the pattern of responding should remain the same as in the initial portion of the test session. However, if the pigeons had acquired a conditional discrimination, the response pattern should change in accordance with the changed order of the key colors. Although the results of this study do not rule out the possibility that the subjects acquired, to some degree, a response sequence, the results suggest that the behavior of pigeons under a repeated-acquisition-of-behavioral-chains procedure is controlled primarily by conditional discriminative stimuli.     

Concept learning by monkeys with video picture images and a touch screen.

Two rhesus monkeys were trained in a same/different task to discriminate digitized computer-stored picture stimuli. The pictures were digitized from 35-mm slides and presented in pairs on a computer monitor. The monkeys were required to touch the pictures and then make a choice response to indicate whether the pictures were identical or nonidentical. The response areas and stimuli were located to the sides of the picture stimuli. Responses were defined and monitored by an infrared matrix touch screen. After learning the same/different task, both monkeys showed performance accuracy with novel picture stimuli similar to that with training picture stimuli. This accurate novel-picture transfer indicates that a same/different concept had been learned, a concept similar to the one they had previously demonstrated in a different apparatus with rear-projected slide stimuli and a response lever.     

视空间和听觉数字记忆的混合广度

Ｆｒｉｃｋ成功地增加了混合通道的广度,其必要条件是同时呈现视觉刺激和反序报告。该文采用干扰更少的Ｃｏｒｓｉ视空间测验,即序列呈现视觉刺激,并用正序报告,进行混合广度的新实验。发现在分离通道报告的条件下其混合广度都明显地高于单一通道的广度,因此Ｆｒｉｃｋ的两个必要条件不总是必需的。这种新的混合广度实验可能对研究工作记忆的中央执行系统有益。比较了刺激呈现模式和被试反应方式对混合广度的影响     

Choice with certain and uncertain reinforcers in an adjusting-delay procedure.

A discrete-trials adjusting-delay procedure was used to investigate the conditions under which pigeons might show a preference for partial reinforcement over 100% reinforcement, an effect reported in a number of previous experiments. A peck on a red key always led to a delay with red houselights and then food. In each condition, the duration of the red-houselight delay was adjusted to estimate an indifference point. In 100% reinforcement conditions, a peck on a green key always led to a delay with green houselights and then food. In partial-reinforcement conditions, a peck on the green key led either to the green houselights and food or to white houselights and no food. In some phases of the experiment, statistically significant preference for partial reinforcement over 100% reinforcement was found, but this effect was observed in only about half of the pigeons. The effect was largely eliminated when variability in the delay stimulus colors was equated for 50% reinforcement conditions and 100% reinforcement conditions. Idiosyncratic preferences for certain colors or for stimulus variability may be at least partially responsible for the effect.     

Do you know where your group is? development of a group-as-a-whole compass. Part I

A therapist's ability to locate the essential dimensions of a group is a critical skill. The literature on group-as-a-whole theory and practice is a rich body of work that reveals a variety of discrete models and approaches with little coordination between them. This paper is an attempt at theory binding. A group-as-a-whole compass is introduced as a spherical motif to integrate varied conceptual understandings of whole-group functioning. The compass, by providing a metapsychological framework, is designed to orient the therapist and theoretician to the myriad ways that group-centered configurations come to life and can be known.     

Molecular contingencies: reinforcement probability

Pigeons obtained food by responding in a discrete-trials two-choice probability-learning experiment involving temporal stimuli. A given response alternative, a left- or right-key peck, had 11 associated reinforcement probabilities within each session. Reinforcement probability for a choice was an increasing or a decreasing function of the time interval immediately preceding the choice. The 11 equiprobable temporal stimuli ranged from 1 to 11 sec in 1-sec classes. Preference tended to deviate from probability matching in the direction of maximizing; i.e., the percentage of choices of the preferred response alternative tended to exceed the probability of reinforcement for that alternative. This result was qualitatively consistent with probability-learning experiments using visual stimuli. The result is consistent with a molecular analysis of operant behavior and poses a difficulty for molar theories holding that local variations in reinforcement probability may safely be disregarded in the analysis of behavior maintained by operant paradigms.     

Behavioral contrast in rats with different reinforcers and different response topographies

Experiment I demonstrated positive behavioral contrast in rats when one of two qualitatively different reinforcers (milk and pellets) was removed from a component of a multiple schedule. The contrast effect was larger and more enduring when milk was removed. Experiment II showed that the rats spent more time on the side of a shuttle-box on which milk was freely available than on the side on which pellets were freely available. Experiment III, a partial replication of Experiment I, failed to demonstrate the contrast effect of Experiment I. Experiment IV demonstrated contrast when two topographically distinct responses, nose-key poking and lever pressing, were required in different components of a multiple schedule. These results extend the conditions that generate behavioral contrast in rats.     

Maintenance of behavior controlling the duration of discriminative stimuli

The maintenance of a response controlling the duration of positive and negative discriminative stimuli in a multiple schedule was examined with respect to the possible consequences of the response: none, escape from the negative stimulus, production of the positive stimulus, and initiation of the reinforcement schedule associated with the latter. The last two seemed to be the major factors in producing and maintaining the response. Escape from the negative stimulus maintained it in most subjects, but only at a much lower level.