Note on changes in response latency following discrimination training in the monkey

Two monkeys were trained to press and hold down a telegraph key in the presence of a red light. Subsequent release of the key in response to a white cross superimposed on the red background was followed by reinforcement. Key release in response to a white circle on the red background was never reinforced. Latencies for the key release response to the reinforced stimulus (cross) were considerably shorter and less variable than those to the unreinforced stimulus (circle).     

Shaping of three-man teams on a multiple DRL-DRH schedule using collective reinforcement

Five three-man teams were conditioned to a multiple DRL-DRH schedule during five daily sessions of 3 hr each. The teams were conditioned on the basis of their cumulative response rate regardless of the contributions of individual members. Two individually conditioned Ss were run under a similar schedule for comparison. Although all teams demonstrated some differentiation of response rate under the two legs of the schedule, this difference was not achieved as rapidly, nor was it as stable, as the differentiation in rates achieved in individually conditioned Ss. Team members displayed a variety of response rates as a result of collective team conditioning. Often, individual response rates interfered with obtainment of team reinforcement. The individual team members displayed little S^D control in comparison with the individually conditioned Ss. In general the results suggest that collective reinforcement is highly inefficient in comparison with procedures employing individual feedback.     

A behaviour modification technique for the hyperactive child

This paper describes a procedure for the conditioning of attending behaviour in a brain-injured hyperactive boy.

Observations of the behaviour of two hyperactive children were made in the classroom setting. These observations were made from an observation bootn adjoining the classroom and provided data on the frequency of occurrence of the following high rate responses: walking, talking, distraction, “wiggling”. Each child was observed for a minimum of ten minutes a day, four days a week. Following several weeks of baseline observation, the conditioning procedure was begun with the expel imental subject. The conditioning trials took place in the classroom setting. During each time interval in which one of the high rate responses did not occur, S received an auditory stimulus (secondary reinforcer). This auditory stimulus had previously been paired with the delivery of candy and pennies. The stimulus was dispensed by a radio device which activated an earphone worn by the subject. At the end of each conditioning trial, S received whatever candy or pennies he had “earned”.

The data show that the control subject showed no significant change in the frequency of occurrence of the high rate responses during the three month period. The experimental subject showed a significant decrease in non-attending behaviour. This reduction in rate was maintained over a four week extinction period.     

Sidman avoidance in the fish

Goldfish trained in a shuttle box under conditions in which changing compartments postponed shock for 20 sec showed a substantial, negatively accelerated increase in rate of crossing. That the avoidance-contingency was responsible for the change in behavior is suggested by the fact that no significant increase in rate of crossing appeared in control animals which were paired with the experimentals and shocked whenever the experimental animals were shocked; there is some evidence, indeed, that the control animals were handicapped in their subsequent adjustment to the avoidance condition. The introduction of a warning stimulus (light) in the last 5 sec of the response-shock interval decreased the rate of crossing in the first 15 sec and increased the rate of crossing in the last 5 sec. Reducing the shock-shock interval from 20 sec to 2.5 sec had no marked effect. The results are compared with those obtained in analogous experiments with higher animals.     

Ratio reinforcement of matching behavior

Three pigeons, previously trained to a high level of accuracy on matching-to-sample procedures, were exposed to various schedules of ratio reinforcement for correct matches. Overall accuracy was lower on fixed ratio than on regular reinforcement. There was a high incidence of errors immediately after reinforcement on fixed ratio schedules with accuracy increasing as the ratio progressed. This increase was found to be inversely correlated with the latency of the observing response to the sample. By contrast, accuracy was high throughout the ratio on a variable ratio schedule.     

Partial negative reinforcement: fixed-ratio escape

Rats were unable to sustain performance when eight bar-presses turned off shock (−FR 8). In a second experiment, thirsty rats were able to maintain a moderate response rate when performance on −FR 8 was also reinforced with water. Some rats continued to bar-press on −FR 8 after withdrawal of positive reinforcement, but at a much lower rate. A possible explanation of the results is that during intermittent escape conditioning in a free-responding situation the absence of shock itself acquires aversive properties.     

Some parameters affecting the distributional properties of operant-level running in rats

Six adult female albino rats were subjected to operations known to increase the frequency of wheel-running. Operations included limited access to wheel, food deprivation, and protracted maintenance on a 24-hr feeding schedule. A distributional analysis of response duration, burst duration, and inter-burst interval showed that the increased frequency in all cases arose mainly from a shortening of the interval between successive bursts. Only short-term food deprivation produced any notable increase in burst length, and even here changes in both speed of the individual responses and in number of responses per burst were slight compared to changes in inter-burst interval.