Changing the response unit from a single peck to a fixed number of pecks in fixed-interval schedules

Each of three pigeons was studied first under a standard fixed-interval schedule. With the fixed interval held constant, the schedule was changed to a second-order schedule in which the response unit was the behavior on a small fixed-ratio schedule (first a fixed-ratio 10 and then a fixed-ratio 20 schedule). That is, every completion of the fixed-ratio schedule produced a 0.7-sec darkening of the key and reset the response count to zero for the next ratio. The first fixed-ratio completed after the fixed-interval schedule elapsed produced the 0.7-sec blackout followed immediately by food. These manipulations were carried out under two different fixed-interval durations for each bird ranging from 3 min to 12 min. The standard fixed-interval schedules produced the typical pause after reinforcement followed by responding at a moderate rate until the next reinforcement. The second-order schedules also engendered a pause after reinforcement, but responding occurred in bursts separated by brief pauses after each blackout. For a particular fixed-interval duration, post-reinforcement pauses increased slightly as the number of pecks in the response unit increased despite large differences in the rate and pattern of key pecking. Post-reinforcement pause increased with the fixed-interval duration under all response units. These data confirm that the allocation of time between pausing and responding is relatively independent of the rate and topography of responding after the pause.     

Fixed-interval limited-hold avoidance with and without signalled reinforcement

Rats trained to lever press on a fixed-interval limited-hold avoidance schedule maintained a pattern of responding similar to that maintained by fixed-interval limited-hold schedules of positive reinforcement. But this positively accelerated pattern of behavior was maintained only when the occurrence of reinforcement was signalled by the presentation of a brief flash of light. This result suggests that the discriminative function of the reinforcer in avoidance is less pronounced than the discriminative function of the reinforcer in escape or positive reinforcement. It also suggests that the distinction between positive reinforcement and avoidance is not superfluous. Although the schedule of reinforcement is an important variable in determining the pattern of behavior, other variables, such as the nature (i.e., stimulus presentation, termination, or omission) of the reinforcer, are also potent determinants of behavior.     

Infantile handling and sex as determinants of the negative reinforcing effects of gentling

Summary BD IX rats were trained to avoid a black and white compartment which was associated with gentling. The rats were given 12 acquisition sessions in which they were stroked if they remained in the critical compartment at the end of the fifteen 20-sec intervals during the 5-min test period. The results indicated that the negative reinforcing effects of gentling were a function of the early handling history and sex of the rat.This research was aided by Grant APA-247 from the National Research Council of Canada. The author thanks David Wood for his active collaboration in conducting the experiment.     

An apparatus for apparent conditioning ofOctopus cyaneus Gray

An ann-out-of-water response was conditioned as an operant inOctopus cyaneus Gray. The response was limited to a vertical tube, 2.54 em i.d, Photoresistive sensors, illuminated with modulated light arranged around the tube above the waterline, detect the presence of an opaque object in the tube. The signal from this response detector is amplified and used to initiate a commercial motor-driven universal feeder according to the reinforcement schedule maintained by the logic control circuit. A sample cumulative record for perfonnance on a CRF schedule is given.     

A circuit to permit an electronic drinkometer to operate during footshock

A circuit to permit an electronic drinkometer to operate during footshock is described. The circuit employs a diode matrix that allows all grid bars to be connected at one point to form one electrode of the drinkometer; it is isolated at another point so as not to shortcircuit the impressed footshock.     

Misuse,abuse, overuse,and unuse of on-line computer facilities by psychologists

This, then, is a very personal and informal view of some of the peculiar trends of computer application in experimental psychology. If there is any single point on which I would prefer to end, it would be a reiteration of my belief that, on the whole, the positive attributes and contributions to our science of on-line computers have far outweighed some of these nagging aggravations. Regardless of what has been done and in what way it has been done, it is certainly better to have done something than never to have done anything at all. Our science, like a computer program, is also contingent and self-adapting, and most minor strategic errors are quickly corrected. But no one can debug a computer program or a major technological movement without at least having pushed the startbutton.     

Error patterns in a chord keyboard response task

Errors in a serial choice-reaction time experiment employing two-finger chord responses to alphabetic stimuli are shown to be distributed in a significantly non-random fashion. Two factors are postulated which are relevant to prediction of the error response. These are the presence or absence of a common finger, and the difference in finger separation, between the actual and the required response. It is suggested that the chord response is coded in terms of a pattern (the distance between the two response components). Responses which mirror the correct response about the centre of the hand are also shown to be significantly more frequent.     

Sleep and overextinction of the GSR component of the orienting response

Overextinction of the GSR component of the orienting response was examined in a sample of 68 socially disturbed adolescents. Continued stimulus repetition beyond the point of habituation resulted in GSR return after 50–60 stimulus presentations. However, division of Ss into sleep and non-sleep groups using behavioral and self-report criteria, failed to support Sokolov’s (1963) notion that overextinction is accompanied by drowsiness. A possible explanation of these results is discussed.