Effects of hunger and VI value on VI pacing

In two experiments, each involving four rats, responses preceded by an inter-response time between 8 and 10 sec in duration were intermittently reinforced. In Experiment I, final performance was compared under two hunger levels, while the frequency of reinforcement was held constant by a VI 5 schedule. In Experiment II, hunger was held constant and VI 3 was compared with VI 8. Both hunger and frequency of reinforcement increased the over-all rate of response, but the exact effects of these operations on temporal discrimination were different for different rats. Usually, a peak “response probability” (IRTs/Op ratio) was obtained 8 to 10 sec after the preceding response, indicating adaptation to the reinforcement contingency, but in some cases this peak was about 2 sec earlier. One rat exhibited unusually pronounced bursting which seemed to alternate with adaptive temporally spaced responding. Prolonged pauses, observable in the cumulative records, particularly following reinforcement, were attributed to the fact that inter-response times greater than 10 sec were not reinforced, so that as the interval of time since the preceding response became discriminably greater than 10 sec, the probability of a response became small.     

VI. Akrasia and conflict

As Elster suggests in his chapter ‘Contradictions of the Mind’, in Logic and Society, akrasia and self‐deception represent the most common psychological functions for a person in conflict and contradiction. This article develops the theme of akrasia and conflict. Section I says what akrasia is not. Section II describes the character of the akrates, analyzing the sorts of conflicts to which he is subject and describing the sources of his debilities. A brief account is then given of the attractions of the akratic alternative: its power to focus or dominate the agent's attention; its being strongly habitual; its having the pull of social streaming: following the charismatic leader, the mechanisms of sympathetic or antipathetic infection, the models of role casting. Following these strategies is by no means pathological: these are relatively automatic (though still voluntary) psychological functions. That is precisely their power and attraction: they provide the conflicted akrates with an action solution, though not one that accords with his preferred judgment.     

Determination of a behavioral transfer function: White-noise analysis of session-to-session response-ratio dynamics on concurrent VI VI schedules

Six pigeons were exposed to concurrent variable-interval schedules in which the programmed reinforcer ratios changed from session to session according to a pseudorandom binary sequence. This procedure corresponded to the stochastic identification paradigm (“white-noise experiment”) of systems theory and enabled the relation between log response ratios in the current session and log reinforcer ratios in all previous sessions to be determined. Such dynamic relations are called linear transfer functions. Both nonparametric and parametric representations of these, in the form of “impulse-response functions,” were determined for each bird. The session-to-session response ratios resulting from the session-to-session pseudorandom binary variations in reinforcer ratios were well predicted by the impulse-response functions identified for each pigeon. The impulse-response functions were well fitted by a second-order dynamic model involving only two parameters: a time constant and a gain. The mean time constant was 0.67 sessions, implying that the effects of abrupt changes in log reinforcer ratios should be 96% complete within about five sessions. The mean gain was 0.53, which was surprisingly low inasmuch as it should equal the sensitivity to reinforcement ratio observed under steady-state conditions. The same six pigeons were subjected to a similar experiment 10 months following the first. Despite individual differences in impulse-response functions between birds within each experiment, the impulse-response functions determined from the two experiments were essentially the same.     

Studies of Emotional Reactions VI. Cardiac Responses

Wild-strain male house mice were fostered at birth onto conspecifics, deer mice, or domestic Norway rats. In adulthood, their flesh-eating preferences were tested by allowing them to feed from freshly asphyxiated conspecifics and either deer mice or rats. The mice ate significantly more conspecific flesh than contraspecific flesh, except when the flesh offered was that of the contraspecies upon which the mouse had been fostered at birth. The failure of cross-species-fostered mice to discriminate between their own species and their foster species in flesh-preference tests is attributed to their having learned early in life to respond to the foster species in the same way they normally respond to conspecifics, that is, by approaching them, investigating them, and, when finding them dead, feeding upon them.     

Section VI: Summary,Conclusions and Recommendations

Abstract

Helping children to use words to express their thoughts and feelings is the goal of psychodynamic group therapy. The subject of this paper was a group of boys in a weekly school-based counseling group. The article explores ways in which the boys could only discharge psychic tension in action and uncovers a fear of using words as a mode of expression. By conceptualizing what he calls “action-talk,” a stage between the use of action and talk which sounds like talk, but is not, the author resolved resistances to progressive communication. The importance of being aware of the therapist’s own need to control the direction of the group, tendency to avoid negative feelings, and the importance of open-ended, talk-based therapy approaches (versus curriculum-based or psychoeducational groups) are discussed.     

Effects of dl-amphetamine under concurrent VI DRL reinforcement

Three adult, food-deprived rats were given IP injections of dl-amphetamine sulfate under DRL and concurrent VI DRL reinforcement schedules. The drug results were as follows.(1) The IRT distributions of DRL responses shifted to the left, but some temporal discrimination remained. (2) The IRT distributions of VI responses shifted slightly to the left. (3) The distinguishing characteristics of VI and DRL IRT distributions were preserved. (4) The frequency distribution of number of VI responses between two consecutive DRL responses was relatively unaffected. (5) Over-all response rates on the two components of the concurrent schedules increased more or less proportionately.These findings imply that the primary behavioral effect of dl-amphetamine was a motor excitatory one. The drug's disruption of timing behavior was not due to a derangement of internal timing mechanisms, nor to interference with the topography or pattern of behavior. Rather, it might be a secondary result of the accelerated emission of overt behavior patterns mediating the temporal spacing of DRL bar presses.