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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).

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Several lines of evidence suggest that the pigeon is near‐sighted for stimuli located in front of its beak and far‐sighted for stimuli located to the sides of its head.

A procedure is described for establishing an operant response in goats. The operanda are two lucite panels which can be transilluminated. The goats press the panels with their muzzles and are reinforced with whole oats. All six subjects showed reliable and accurate performance in brightness discrimination, including cessation of responding during time‐out periods.

Preening in four pigeons was observed and recorded during operant level determinations, continuous and variable interval reinforcement, and extinction. The rate at which preening responses occur seems to be controlled by reinforcement in the same way as other operant behavior. Preening during VI reinforcement and extinction appeared to be similar to preening in many natural situations. With respect to the part of the body preened, considerable stereotypy of responding was shown by all birds, particularly during VI training; there was, however, a conspicuous absence of consistency in the development of stereotypy both within and between individual birds, perhaps due to the nature of the response.

Extinction in the presence of each of two stimuli reduces the rate of pecking in the presence of each of them to zero or near zero. When, however, pecking a third stimulus is reinforced, responding is resumed under the other stimuli, and more responses are made to the stimulus least associated with extinction.

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