Frequency discrimination near masked threshold

Frequency DLs (Δf) at 1000 Hz were obtained in quiet and under masking conditions similar to those used in pitch-shift experiments, narrow-band noise at levels of 60, 80, and 100 dB SPL and tones at 15 dB SL or less. The Δfs were obtained by means of a tracking task in which the S controlled the input voltage to a frequency modulator. Characteristic improvement was seen when Δf was plotted as a function of sensation level. However, noise level itself was a significant factor, with more intense noise resulting in larger Δfs for tones of equal sensation level re masked threshold. This departure from previous findings is attributed to the signal and noise levels used, although the possibility exists that it is due to the use of modulated tones.     

On the rate of stimulus occlusion during intermittent retinal stimulation

The CFF was determined with three sectored disks, each of which corresponded to one of the three rings in a Helmholtz disk. The fusion frequency is identical for all three rings of a Helmholtz disk but with the three sectored disks it was found that the rate of stimulus occlusion is a major factor in determining the CFF. It was tentatively concluded that the effect was not a consequence of different stimulus wave-forms. The phenomenon appears to have been reported late in the last century.     

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.     

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.