Punishment by noise in an alternative response situation

Operant responses of human subjects were conditioned according to a variable-interval schedule of positive reinforcement. A brief noise was delivered as punishment for each of the responses. The noise suppressed the punished responses more when an alternative unpunished response was concurrently available than when only a single punished response was available. This finding extends the generality of a previous study that had used a period of extinction rather than the brief noise as the punishing stimulus.     

Punishment of temporally spaced responding

The responses of pigeons were maintained by a DRL schedule of food reinforcement. With this schedule, responses were reinforced only when a fixed period of time elapsed without an intervening response. Punishment of all responses reduced the frequency of these responses as a direct function of the punishment intensity. As a consequence of the increased temporal spacing of responses, more reinforcements resulted during punishment. Under progressively higher intensities of punishment, the reinforcement frequency increased to a maximum value and then decreased at the highest intensities. The increased frequency of reinforcement which resulted during punishment did not counteract the suppressive effect of punishment, nor did it lead to a low response rate after punishment was removed. Punishment did not reduce the inter-response time distribution uniformly, but rather especially reduced the number of short inter-response times. Even at the low punishment intensities, the number of short inter-response times was considerably reduced. After punishment was discontinued, performance recovered almost completely after a compensatory burst. The number as well as the temporal pattern of responses returned to normal.     

Elimination of behavior of mental patients by response-produced extinction

Mental hospital patients were conditioned to respond at a high rate. Then an attempt was made to eliminate the response by means of a mild punishment consisting of a period of timeout from reinforcement (response-produced extinction). When only one response was available for obtaining the reinforcement, the mild punishment was not effective in eliminating that response. When an alternative response was also made available for obtaining the reinforcement, the mild punishment was completely effective. It appears that even very mild punishment may be effective if the over-all frequency of reinforcement can be maintained by means of an alternative unpunished response.     

Conditioning of the aggressive behavior of pigeons by a fixed-interval schedule of reinforcement

Operant reinforcement of aggression was studied in food-deprived pigeons by delivering food for attacks against a target pigeon. The food was delivered according to a fixed-interval schedule and attack behavior was recorded automatically. Attack could be conditioned and extinguished, and the proportion of time spent in attack was a direct function of the frequency of reinforcement of the attack. The fixed-interval schedule produced an increasing rate of attack during the interval between food reinforcements. This positive curvature was an inverse function of the duration of the interval. The findings revealed that the duration and temporal patterning of the complex social behavior of attack can be influenced in a substantial and predictable manner by the schedule and frequency of operant reinforcement.     

Temporal patterns of sexual behavior in rabbits as determined by an automatic recording technique

Sexual behavior between rabbits was automatically recorded by means of electrodes attached externally to the unrestrained animals. Current flowed only when the animals came into physical contact; the duration and amplitude of the current flow provided a means of automatic differentiation between sexual and other types of physical contact. Various temporal aspects of sexual behavior were revealed: (1) copulation was preceded by a series of thrusts that occurred at a constant frequency of 13 to 14 thrusts per sec; (2) the duration of a copulation was about 1.5 sec and could be as brief as 0.3 sec; (3) copulation was much more likely during the hours between dusk and dawn despite constant illumination; (4) copulations occurred in groups or “runs” characterized by many copulations within a few hours; (5) each run began with a high rate of copulation that often decreased over time; (6) between runs, several hours or days passed with little or no sexual activity; and (7) a run of copulations was noted at the end of every 16- to 20-day period (which corresponds to the known period of pseudopregnancy in rabbits) whether or not other runs occurred within this period.     

Stimulus-response incompatibility eliminates inhibitory cueing effects with saccadic but not manual responses

There are thought to be two forms of inhibition of return (IOR) depending on whether the oculomotor system is activated or suppressed. When saccades are allowed, output-based IOR is generated, whereas input-based IOR arises when saccades are prohibited. In a series of 4 experiments, we mixed or blocked compatible and incompatible trials with saccadic or manual responses to investigate whether cueing effects would follow the same pattern as those observed with more traditional peripheral onsets and central arrows. In all experiments, an uninformative cue was displayed, followed by a cue-back stimulus that was either red or green, indicating whether a compatible or incompatible response was required. The results showed that IOR was indeed observed for compatible responses in all tasks, whereas IOR was eliminated for incompatible trials—but only with saccadic responses. These findings indicate that the dissociation between input- and output-based forms of IOR depends on more than just oculomotor activation, providing further support for the existence of an inhibitory cueing effect that is distinct to the manual response modality.