Auditory generalization gradients for response latency in the monkey

Two monkeys were trained to press and hold a response key in the presence of a light and to release it at the onset of a pure tone. Initially, all responses with latencies shorter than 1 sec were reinforced without regard to the frequency of the pure tone, and the intensity of the pure tone that resulted in equal latencies at each frequency was determined. The second stage of the experiment consisted of discrimination training, during which releases to one pure-tone frequency (positive stimulus) were reinforced and releases to a second frequency (negative stimulus) were extinguished. Median latencies to the negative stimulus slowly increased as did the variability of the latency distribution for the negative stimulus. There was no evidence of a concurrent decrease in latencies to the positive stimulus indicative of behavioral contrast. The third part of the experiment consisted of determining maintained generalization gradients by increasing the number of nonreinforcement stimuli. The gradients that eventually resulted showed approximately equal latencies to all frequencies of the negative stimulus and shorter latencies to the positive stimulus frequency.     

A demonstration of auto-shaping with monkeys

The Brown-Jenkins auto-shaping procedure for pigeons was found applicable to monkeys. Repeated pairings of lighted keys with reinforcement generated key-pressing behavior. The animals rapidly learned a simultaneous light-dark discrimination. The topographies of key-pressing and magazine behavior differed; the food tray was not illuminated.     

Some effects of discriminative training with equated frequency of reinforcement

Pigeons were exposed to a multiple schedule which provided equally frequent reinforcement in the presence of two stimuli but which produced markedly different rates of key-pecking. Generalization gradients were displaced away from the stimulus associated with the lower rate of key-pecking. Another group of pigeons had similar training, except that a low rate of key-pecking was established in a stimulus with a much higher frequency of food reinforcement. In this case, the generalization gradients were not affected by the training on the schedule producing a low response rate.     

Suppression of behavior by timeout punishment when suppression results in loss of positive reinforcement

This investigation, using rats as subjects and punishment by timeout for responses maintained on a ratio schedule, sought to determine whether behavior would be suppressed by timeout punishment when such suppression also reduced reinforcement density or frequency. A series of experiments indicated that timeout punishment suppressed responding, with the degree of suppression increasing as a function of the duration of the timeout period. Suppressive effects were found to decrease as a function of increases in deprivation (body weight) and were eliminated when the punished response also was reinforced. It was concluded that timeout can produce aversive effects even when loss of reinforcement results. An alternative interpretation of the findings, based on the effects of extinction periods and delay of reinforcement on chained behavior, was discussed.     

Further evidence of a sensory-tonic interaction in pigeons

The five pigeons in Group 1 were given successive intradimensional discrimination training in which responses to a line of 49 degrees were reinforced on a variable-interval schedule and responses to a line of 33 degrees were not reinforced. Subsequent generalization testing with other line orientations revealed a peak shift from the positive stimulus in the direction away from the negative stimulus in all subjects. The four pigeons in Group 2 received successive discrimination training with the 49 degrees value on the key during both stimuli. During the negative stimulus, however, the floor was tilted 16 degrees counterclockwise. When tested (with the floor flat) these subjects showed peak shifts similar to those observed with Group 1. A third group of three pigeons, given successive interdimensional discrimination training with the 49 degrees line as the positive stimulus and the absence of the line as the negative, showed no peak shift in a subsequent generalization test. It was concluded that tilting the floor on which the pigeon stood systematically distorted the bird's visual perception of the orientation of the line in a manner consistent with the results of other studies in this laboratory.     

Stimulus control in the experimental study of cooperation

The cooperative responses of pairs of human subjects were reinforced under several stimulus conditions in two settings designed to require a "social" response, i.e., where at least one of the two persons is responding to the behavior of the other. The first task, designed by Lindsley and Cohen, required individual responses within 0.5 sec of one another for reinforcement. The second (modified) task required a delay of 3 sec between individual responses. To determine dependence of cooperation on social stimuli, rates of cooperative behavior on these tasks were compared in the presence and absence of a stimulus indicating to each subject the other's response and a stimulus which indicated the duration of the timeout after reinforcement. The results indicated that only in the modified task was a high rate of cooperation always contingent upon the presence of the social stimuli.     

Facilitation and suppression of human loss-avoidance by signaled, unavoidable loss

A 15-sec stimulus followed by unavoidable monetary loss was presented to human subjects who were avoiding loss on a free-operant schedule. As has been observed in studies where shock is the aversive event, initial reactions to the pre-loss stimulus were transient increases in overall and stimulus rates. Unlike shock studies, continued training produced decreased rates, in the presence of the 15-sec stimulus, which were maintained in two of three subjects. Subsequent observations indicated that lowered rates were a function of the subject's rate of avoidance responding, the duration of the stimulus, and the scheduling of avoidable losses. Increasing the duration of the stimulus eliminated lowered rates in the presence of the stimulus and subsequent exposures to conditions which previously produced lowered rates did not result in recovery of the phenomenon. Introduction of the pre-loss stimulus on an extinction baseline (avoidable losses were omitted), however, reinstituted lowered rates. It is proposed that the pre-loss stimulus assumed discriminative control over low rates because responding in the presence of the stimulus was ineffective in avoiding the unavoidable loss. Recovery from lowered rates is attributed to the occurrence of avoidable losses during the stimulus period, and maintenance of lowered rates on the extinction schedule to the omission of such avoidable losses.     

Magnitude and frequency of reinforcement and frequencies of interresponse times

The relative magnitude and relative frequency of reinforcement for two concurrent interresponse times (1.5 to 2.5 sec and 3.5 to 4.5 sec) were simultaneously varied in an experiment in which pigeons obtained grain by pecking on a single key. Visual discriminative stimuli accompanied the two time intervals in which reinforcements were arranged by a one-minute variable-interval schedule. The resulting interresponse times of each of three pigeons fell into two groups; "short" (1.0 to 2.5 sec) and "long" (3.0 to 4.5 sec). Steady-state relative frequencies of these interresponse times were orderly functions of both reinforcement variables. The combined effects of both independent variables were well summarized by a linear function of one variable, relative access to food. Unlike corresponding two-key concurrent variable-interval schedules, the present schedule did not produce an equality between the relative frequency of an operant and either the relative magnitude or the relative frequency of reinforcement of that operant. A tentative account is provided for this difference between one-key and two-key functions.     

Performance of two species of quail on basic reinforcement schedules

Two bobwhite quail (Colinus virginianus) and two Japanese quail (Coturnix coturnix japonica) were trained to peck a response key to obtain food. In general, performance on fixed ratio 20 and variable- and fixed-interval 60-sec schedules was comparable to the response patterns of other species under these schedules.     

A comparison of escape and avoidance conditioning in wild and domesticated rats

In the first of two experiments, three cotton rats (Sigmodon hispidus) and three albino rats were exposed to instrumental escape, unsignaled avoidance, and signaled avoidance, in that order. All subjects learned the escape procedure quickly, with the albino rats having generally shorter latencies, higher response rates, and requiring fewer sessions to reach the criterion. When the avoidance contingency was introduced, the cotton rats continued to respond almost entirely in the presence of the shock, whereas the albino rats responded in its absence, thus displaying effective avoidance behavior. Introduction of a pre-aversive stimulus did not improve the performance of the cotton rats. In the second experiment, five cotton rats and four albino rats were exposed to a free-operant (Sidman) avoidance procedure with a shock-shock interval of 3 sec and a response-shock interval of 20 sec. The cotton rats initiated responding at lower shock intensities than the albino rats, but their asymptotic avoidance responding was far less effective.