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D Anger

Publications and source records attributed to D Anger.

13 recordsLinked to original sources

Reinforcement of inhibition.

A differential-reinforcement-of-other-behavior (DRO) schedule with trials and delayed reinforcement was investigated. Periodically a wheel was briefly available to rats, followed six seconds later by brief availability of a bar. Variable-ratio food reinforcement of wheel turns was adjusted to give 95% turns. After variable-ratio-five reinforcement of bar presses produced 100% pressing, then separate ratio schedules were used for presses following turns (turn presses) and presses following nonturns (nonturn presses). Increasing nonturn-press reinforcements decreased turns, even though total reinforcements increased. Reversal by decreasing nonturn-press reinforcements raised turns, though with hysteresis. Thus food reinforcement increased nonturns even though delayed six to ten seconds after nonturns, a delay that greatly reduces response reinforcement. Those and other results indicate that the turn decrease was not due to reinforcement of competing responses. Evidence against other alternatives, and the reduction of responding by increased reinforcement, indicate that the term inhibition is appropriate for the phenomenon reinforced. Response-specific inhibition appears appropriate for this particular kind, since its effects are more specific to particular responses than Pavlovian conditioned-inhibition. Response-specific inhibition seems best considered a behavioral output comparable to responses (e.g., both reinforcible) but with important properties different from responses (e.g., different reinforcement-delay gradients).

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Behavior changes during repeated eight-day extinctions.

Pigeons were given repeated two-day conditionings alternating with eight-day extinctions using a trial procedure. One group had different key colors during each of the first five conditioning-extinction pairs; another group had the same key color throughout. Total extinction responses of both groups were quite constant over successive extinctions. This finding differs from the rapid declines found in most previous studies with bar-press and key-peck responses. The difference probably was due to our longer extinctions, because responses early in each extinction did decrease. However, that decrease was neutralized by increases in responses late in each extinction. The two opposite changes indicate the influence of two different factors during repeated extinctions, with neither factor having much stimulus specificity. The reduction of early responses may result from feeding changes confounded with extinction. The increase in later extinction responses may result from a decrease in the effect of unreinforced responses after their repeated occurrence.

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The effect upon simple animal behavior of different frequencies of reinforcement, Part II: separate control of the reinforcement of different IRTs.

Rats' responding was stabilized for over 35 days on 4-min variable-interval reinforcement. Reinforcements per hour for 4-sec wide classes of interresponse times were then separately controlled by adjusting those for each class to the variable-interval values that had just prevailed. This produced little or no change in interresponse times, indicating that the new procedure was substantially equivalent to a variable-interval schedule. The variable-interval schedule produced a high and stable conditional probability of interresponse times in the 0- to 4-sec class, associated with a peak in reinforcements per hour for this class. Reducing the reinforcements per hour for this class while raising that for another class (by 3.3 reinforcements per hour) significantly reduced the conditional probability of 0- to 4-sec interresponse times. Restoring the 3.3 reinforcements per hour to the 0- to 4-sec class significantly elevated the conditional probability of interresponse times in this class. Hence, it is concluded that the distribution of interresponse times produced by a subject during some variable-interval schedules is determined partly by the relative reinforcement of different interresponse times that the variable-interval schedule provided.Reprinted from Part II of the Final Report of Research under Contract DA-49-007-MD-408 with the Medical Research and Development Board, Office of the Surgeon General, Department of the Army, 31 December 1954. Edwin B. Newman, Responsible Investigator; Douglas Anger, Research Assistant and author of report. Experimental work done in the Psychological Laboratories of Harvard University.

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The effect of discrimination training on responses to a new stimulus.

Most previous research on the effect of the duration of preceding discrimination training on responding to a new stimulus has measured the responding during extinction. To reduce effects originating in the extinction procedure itself, the present study assessed the effect of discrimination training on responses to a new negative stimulus added during continued discrimination training. Pigeons were given a new negative stimulus (blue key) after 0, 1, 3, or 9 days of discrimination training with a yellow key as the positive stimulus, and both a green key and a red key as negative. Fewer responses were made to the blue key when it was introduced after nine days of discrimination training than after less discrimination training. That effect of long discrimination training agrees with reported results from extinction tests. However, the effect of briefer discrimination training in the present study differed from reported results with extinction testing. It appears that testing during continued discrimination training eliminates a distortion present in extinction tests of the effect of discrimination training on responding to a new stimulus.

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