Group Dynamics—Boon or Bane?

In our society an increasingly greater emphasis is being placed on group interaction and decision-making. Persons participating in such a process often use the term “group dynamics” to describe what is thought to be a social-psychological phenomenon. This article discusses some of the elements of “true” group characteristics and effects, and their possible existence in “group dynamic” situations. The article also deals with the implications of the effects of these elements in “group dynamic” environments on educational and administrative leadership and decision-making.     

The uniqueness and significance of simple structure demonstrated by contrasting organic “natural structure” and “random structure” data

The study compares the extent to which naturally structured data and artificial, relatively random data (both with the same basic parameters) produce simple structure factors which are uniquely determined. Two examples of unstructured matrices were compared with the ball problem matrix. The results show that an oblique position of maximum hyperplane count in the structured data differs from that in the unstructured by reaching a significantly more unique position in terms of the exactitude with which it is re-discoverable when starting from different positions, and by reaching (at the maximum) a significantly higher hyperplane count.     

Persistent behavior maintained by unavoidable shocks

Squirrel monkeys were trained on a multiple schedule in which 10-min periods on a continuous shock avoidance schedule, indicated by a yellow light, alternated with 10-min periods on a 1.5-min variable interval schedule of food reinforcement (VI 1.5). A white light indicated that VI 1.5 was in effect, except for the middle 2 min of the period on VI 1.5, in which a blue light appeared and terminated with the delivery of a 0.5-sec unavoidable shock. Stable response rates developed in the avoidance and VI 1.5 components. However, the highest response rates occurred in the blue, preshock stimulus. A series of experiments showed that responding in the blue stimulus persisted even when responding had been extinguished on both the VI schedule of food reinforcement and the shock avoidance schedule. Responding in the blue stimulus ceased when the blue stimulus terminated without shock or when it terminated with a response-contingent shock. Each time responding ceased, it was restored by terminating the blue stimulus with an unavoidable shock. When the blue stimulus was on throughout each session and unavoidable shocks were delivered at regular 10-min intervals, responding was well maintained. These results show that in monkeys that have been trained on a continuous avoidance schedule, unavoidable shocks can maintain responding even under conditions where responses have no programmed consequences.     

Reinforcement of least-frequent sequences of choices

When a pigeon's choices between two keys are probabilistically reinforced, as in discrete trial probability learning procedures and in concurrent variable-interval schedules, the bird tends to maximize, or to choose the alternative with the higher probability of reinforcement. In concurrent variable-interval schedules, steady-state matching, which is an approximate equality between the relative frequency of a response and the relative frequency of reinforcement of that response, has previously been obtained only as a consequence of maximizing. In the present experiment, maximizing was impossible. A choice of one of two keys was reinforced only if it formed, together with the three preceding choices, the sequence of four successive choices that had occurred least often. This sequence was determined by a Bernoulli-trials process with parameter p. Each of three pigeons matched when p was ½ or ¼. Therefore, steady-state matching by individual birds is not always a consequence of maximizing. Choice probability varied between successive reinforcements, and sequential statistics revealed dependencies which were adequately described by a Bernoulli-trials process with p depending on the time since the preceding reinforcement.     

The reinforcement of short interresponse times

Five contingencies were superimposed successively on a variable-interval schedule of reinforcement. In each of the resulting conditions, a different short, interresponse time was reinforced and an interresponse-time distribution was obtained from each of three pigeons. The lower bound of the reinforced interresponse times ranged from 0.3 to 2.4 sec. The resulting distributions were combined, according to a rationale based upon concurrent operants, induction, and a property of variable-interval schedules, to describe the interresponse-time distributions from a variable-interval schedule.     

Changeover delay and concurrent schedules: some effects on relative performance measures

The pigeon and the rat partition total response output between both schedules of a concurrent variable-interval pair. The quantitative nature of a partition seems critically dependent on the relative rates with which the two schedules provide reinforcements for responding, in addition to the changeover delay. The manner in which the changeover delay controls the partition was studied by varying the duration of the changeover delay from 0 to 20 sec with each of two pairs of concurrent variable-interval schedules, viz., Conc VI 1.5-min VI 1.5-min and Conc VI 1-min VI 3-min. Rats served as the subjects and brain stimulation was employed as the reinforcer. When the schedules were Conc VI 1.5-min VI 1.5-min, relative response rate approximated 0.50 at all values of the changeover delay. When the schedules were Conc VI 1-min VI 3-min, relative response rate, computed with respect to the VI 1-min schedule, increased when the duration of the changeover delay increased. Changeover rate decreased when the duration of the changeover delay increased. The decrease was the same for both VI schedules of the Conc VI 1.5-min VI 1.5-min pair but was more rapid for the VI 3-min schedule of the Conc VI 1-min VI 3-min pair.     

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