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.     

A general rotation criterion and its use in orthogonal rotation

Measures of test parsimony and factor parsimony are defined. Minimizing their weighted sum produces a general rotation criterion for either oblique or orthogonal rotation. The quartimax, varimax and equamax criteria are special cases of the expression. Two new criteria are developed. One of these, the parsimax criterion, apparently gives excellent results. It is argued that one of the most important factors bearing on the choice of a rotation criterion for a particular problem is the amount of information available on the number of factors that should be rotated. This research was supported by the National Research Council of Canada research grant 291-13 to Dr. G. A. Ferguson.     

The effect of pressurized air in establishing discriminative response suppression in stump-tailed macaques

Pressurized air was repeatedly associated with one of two frequencies of flashing light during performance of a VI 30-sec positive reinforcement schedule by stump-tailed monkeys. As revealed by the relative suppression of bar presses to each of the two visual stimuli, the Ss learned to discriminate between the different flicker frequencies. However, they also showed signs of adapting to the airblast during the course of training, and its location had to be changed in order to maintain discriminative suppression.     

The effects of area and perimeter on detection rates

The detection of luminance increments in a homogeneously lighted field was studied as a function of the area and perimeter of the luminance increment. Sixteen targets representing all possible combinations of four values of area and four values of perimeter were foveally presented. Exposure durations were short (25 to 40 msec). Results of both an analysis of variance and linear discriminant analysis indicated that detection probability increases as area increases, but neither variations in perimeter nor perimeter-area combinations produced effects that were significant oyer the experiment as a whole. The linear discriminant analysis revealed individual differences in the effects of perimeter and area on detection probability. Results were contradictory to Kristofferson’s (1957) “element contribution theory” and gave only slight support to Hecht’s (Lamar, Hecht, Shlaer, & Hendley, 1947) “border-quantum theory.”     

Experimental control of superstitious responding in humans

Superstitions were demonstrated with human subjects when presses on one button were reinforced on a VI 30-sec schedule while presses on a second were never reinforced. Superstitious responding, on the second button, was often maintained because presses on that button were frequently followed by reinforcement for a subsequent press on the first button. The introduction of a changeover delay (COD), which separated in time presses on the second button and subsequent reinforced presses on the first button, reduced or eliminated the superstitious responding of these subjects. Some complex superstitions were also demonstrated with other subjects for which the COD was in effect from the beginning of the session.     

Concurrent performances: a baseline for the study of reinforcement magnitude

When a pigeon's pecking on a single key was reinforced by a variable-interval (VI) schedule of reinforcement, the rate of pecking was insensitive to changes in the duration of reinforcement from 3 to 6 sec. When, however, the pigeon's pecking on each of two keys was concurrently reinforced by two independent VI schedules, one for each key, the rate of pecking was directly proportional to the duration of reinforcement.     

The effect of abnormal displacement of the retinal image during eye movements

The displacement of the images on the retina that results from a turning of the eye does not lead to an apparent motion of what is seen, It has been generally assumed that this is due to a compensating process which takes eye movement into account and serves to discount those image displacements that result from eye movements, It follows from this view that an abnormal image displacement, that is, an image displacement that is larger or smaller than the causing eye movement would warrant, should lead to an experienced displacement of the target. Abnormal image displacement was produced by placing the eye in the converging or diverging bundle of rays from a point source that form behind a strong positive lens; this arrangement yielded a disc-shaped image, the projection of the pupil onto the retina, which displaced abnormally during eye movements. By changing the position of the eye along the axis of the lens in relation to the crossing point of the bundle, the degree to which the displacement was abnormal could be varied, For various displacement rates ranging from 25% to 120 and 400% of normal, abnormal displacements produced by incidental eye movements remained unnoticed, Only where eye movements were intentional did some of our Ss report shifts of the perceived image. It is suggested that the organism copes with the image displacement resulting from the ever-present incidental eye movements not by compensation but by ignoring them.