Dimensions of the Mysticism Scale: Confirming the Three-Factor Structure in the United States and Iran

In a mostly Christian American sample (N = 1,379), confirmatory factor analysis of Hood's (1975) Mysticism Scale verified the existence of Stace's (1960) introvertive and extrovertive dimensions of mystical phenomenology along with a separate interpretation factor. A second study confirmed the presence of these three factors in not only another group of Americans (N = 188), but also in a sample of Iranian Muslims (N = 185). Relationships of the introvertive and extrovertive factors with the interpretation factor were essentially identical across these two cultures, but the Americans displayed a stronger association between the two phenomenology factors. In both samples, the interpretation factor correlated positively with an intrinsic and negatively with an extrinsic religious orientation, and the introvertive factor predicted psychological dysfunction. Associations of the interpretation factor with relative mental health appeared only in the Iranians. These data offered general support for Stace's phenomenology of mysticism, although the ineffability he linked with interpretation proved to be as much or even more a feature of the introvertive experience, as hypothesized by Hood.     

The effects of a local negative feedback function between choice and relative reinforcer rate

Four pigeons were trained on two-key concurrent variable-interval schedules with no changeover delay. In Phase 1, relative reinforcers on the two alternatives were varied over five conditions from .1 to .9. In Phases 2 and 3, we instituted a molar feedback function between relative choice in an interreinforcer interval and the probability of reinforcers on the two keys ending the next interreinforcer interval. The feedback function was linear, and was negatively sloped so that more extreme choice in an interreinforcer interval made it more likely that a reinforcer would be available on the other key at the end of the next interval. The slope of the feedback function was -1 in Phase 2 and -3 in Phase 3. We varied relative reinforcers in each of these phases by changing the intercept of the feedback function. Little effect of the feedback functions was discernible at the local (interreinforcer interval) level, but choice measured at an extended level across sessions was strongly and significantly decreased by increasing the negative slope of the feedback function.     

Nonstable concurrent choice in pigeons

Six pigeons were trained on concurrent variable-interval schedules in which the arranged reinforcer ratios changed from session to session according to a 31-step pseudorandom binary sequence. This procedure allows a quantitative analysis of the degree to which performance in an experimental session is affected by conditions in previous sessions. Two experiments were carried out. In each, the size of the reinforcer ratios arranged between the two concurrent schedules was varied between 31-step conditions. In Experiment 1, the concurrent schedules were arranged independently, and in Experiment 2 they were arranged nonindependently. An extended form of the generalized matching law described the relative contribution of past and present events to present-session behavior. Total performance in sessions was mostly determined by the reinforcer ratio in that session and partially by reinforcers that had been obtained in previous sessions. However, the initial exposure to the random sequence produced a lower sensitivity to current-session reinforcers but no difference in overall sensitivity to reinforcement. There was no evidence that the size of the reinforcer ratios available on the concurrent schedules affected either overall sensitivity to reinforcement or the sensitivity to reinforcement in the current session. There was also no evidence of any different performance between independent and nonindependent scheduling. Because of these invariances, this experiment validates the use of the pseudorandom sequence for the fast determination of sensitivity to reinforcement.     

Effects of response-allocation constraints on multiple-schedule performance

Four pigeons were trained on multiple variable-interval schedules in which components alternated after a fixed number of responses had been emitted. In Part 1, each component change occurred after 20 responses; in Part 2, the number was 40; and in Part 3, the number of responses before change was 10. Component reinforcer rates were varied over five experimental conditions in each of Parts 1 to 3. Component response rates decreased as the specified number of responses per component was increased. However, the relation between component response-rate ratios and component reinforcer-rate ratios was independent of the specified number of responses per component, and was similar to that found when components alternate after fixed time periods. In the fourth part of the experiment, the results from Parts 1 to 3 were systematically replicated by keeping the component reinforcer rates constant, but different, while the number of responses that produced component alternation was varied from 5 to 60 responses. The results showed that multiple-schedule performance under component-response-number constraint is similar to that under conventional component-duration constraint. They further suggest that multiple-schedule response rates are controlled by component reinforcer rates and not by principles of maximizing overall reinforcer rates or meliorating component reinforcer rates.     

Divided stimulus control: Which key did you peck,or what color was it?

Responding on concurrent schedules produced a conditional discrimination (Phases 1 and 2), asking either which peck produced the event, or which color the keys were when the event was produced. In Phases 3 and 4, reinforcer delivery or a delay in blackout was interpolated between responding and the conditional discrimination. In Phase 1, location versus color discrimination accuracy was controlled by the relative reinforcer frequency for correct responses to these questions (divided stimulus control). In Phases 2 to 4, relative reinforcer frequency for correct responses to these questions was .5, and the relative frequency with which concurrent‐schedule responses produced the questions was varied. This variation had no clear effect on the accuracy of reporting Location or Color. These results are consistent with the model of divided control suggested by Davison and Elliffe (2010). Arranging a 3‐s reinforcer between responding and choice decreased both color and location accuracy, but a 3‐s delay only decreased location accuracy. Thus, in concurrent‐schedule performance, both ambient stimuli prior to a reinforcer and the location of the just‐reinforced response are available as discriminative stimuli following the reinforcer. Control of postreinforcer responding is divided between these according to their association with the relative frequency of subsequent reinforcers.     

Patterns in Father Presence and Engagement in Mongolia: A Historical Cross-Sectional Study

Journal of Child and Family Studies - Many households in Mongolia are facing increased livelihood and financial insecurity due to rapid social, economic, political, and climate changes. There is...     

Being there on time: Reinforcer effects on timing and locating

In research on timing, reinforcers often are assumed to influence discrimination of elapsed time. We asked whether changes in choice used to measure timing arise because of joint control by elapsed time and reinforcers, rather than from the direct modification of control by elapsed time by reinforcers. Pigeons worked on a concurrent-choice task in which 1 response was 9 times more likely to produce a reinforcer, reversing between locations when 19 s had elapsed since the marker event. Across conditions, we manipulated the percentage of reinforcers arranged before the probability reversal from 5 to 95%. These changes in reinforcer percentages altered control by location-based elements of the contingency, but not by time-based elements. Choice was well described by a model that assumes that control by the contingency is weakened by generalization across the time and location of reinforcers, and that these generalizations become more likely at later times since a marker. These findings add to a growing body of research that suggests that reinforcers share the same function as other environmental events in determining how the environment controls behavior.     

Travel time and concurrent-schedule choice: retrospective versus prospective control

Six pigeons were trained on concurrent variable-interval schedules in which two different travel times between alternatives, 4.5 and 0.5 s, were randomly arranged. In Part 1, the next travel time was signaled while the subjects were responding on each alternative. Generalized matching analyses of performance in the presence of the two travel-time signals showed significantly higher response and time sensitivity when the longer travel time was signaled compared to when the shorter time was signaled. When the data were analyzed as a function of the previous travel time, there were no differences in sensitivity. Dwell times on the alternatives were consistently longer in the presence of the stimulus that signaled the longer travel time than they were in the presence of the stimulus that signaled the shorter travel time. These results are in accord with a recent quantitative account of the effects of travel time. In Part 2, no signals indicating the next travel time were given. When these data were analyzed as a function of the previous travel time, time-allocation sensitivity after the 4.5-s travel time was significantly greater than that after the 0.5-s travel time, but no such difference was found for response allocation. Dwell times were also longer when the previous travel time had been longer.