Suppression of VMH-lesion-induced reactivity and aggressiveness in the rat by stimulation of lateral septum, but not medial septum or cingulate cortex

Animals made vicious with bilateral ventromedial hypothalamic lesions had bipolar electrodes implanted unilaterally in the lateral septum, medial septum, or cingulate cortex. Four days later, the animals' reactivity and aggressiveness were evaluated 5 min before, during, and 5 min after stimulation at 20 micronA (60 Hz, sine wave). Lateral septal stimulation suppressed reactivity and aggressiveness by almost 80% compared with pre- and poststimulation levels. Stimulation of neither the cingulate cortex nor the medial septum produced a change reliably different from that seen in unstimulated control animals. Further tests with stimulation of the lateral septum at the 20-micronA level showed that neither rewarding self-stimulation nor disruption of ongoing water drinking was produced. These results are congruent with evidence from lesion studies that the lateral septum normally acts to suppress reactivity and aggressiveness in the rat; they do not support previous suggestions that the medial septum is involved in the modulation of these behaviors.     

Development of binocular fixation in human infants

Two experiments measured changes in binocular eye alignment from 1- to 6-month-old human infants. In Experiment 1 changes in binocular eye alignment were recorded from 1, 2, and 3 month olds using corneal photography. A luminous target was moved along the infant's midline at one of two constant speeds. Infants at all three ages showed some evidence of appropriate changes in binocular eye alignment (convergence as the target approached and divergence as the target receded). The likelihood of appropriate convergence and divergence increased with age, as did the ability to respond appropriately to the faster target motion. A measure of convergence lag (further decrease in interpupillary distance after target motion had ended) was obtained for trials on which the target approached the infant. Convergence lag decreased with age and was greater on trials at the faster target speed until 3 months of age. Experiment 2 measured the responses of 3, $\text{4}\text{1}\text{2}$, and 6 month olds as a wedge prism was placed alternately in front of each eye. The prism displaced the image nasally (either 2.5° or 5°), creating inappropriate binocular eye alignment. A refixation eye movement in response to the prism was not present consistently until 6 months of age. Hypotheses as to the mechanism controlling infant binocular eye alignment are discussed with respect both to the present findings and to findings from human adults and animals.     

TEACHING COIN EQUIVALENCE TO THE MENTALLY RETARDED1

A program was designed to teach coin equivalence to mentally retarded adolescents. Coin equivalence was defined as choosing several different combinations of coins to equal specified target values. A pretest-posttest matched-groups design was employed with an experimental group receiving the monetary training, and a no-training control group. A multiple baseline across coin-counting responses was also incorporated in the experimental group. Training was divided into six stages, each teaching one specific method of combining coins to equal 10 target values from 5¢ through 50¢. A three-component response chain was used, requiring (a) naming, (b) selecting and counting, and (c) depositing target monetary values into a coin machine. Experimental subjects improved significantly in coin equivalence performance and maintained their skill on follow up tests; control subjects did not.     

Serial-position effects in motor short-term memory

This study examined the effect of the length of a series of movements on the recall of those movements. Subjects (n = 45) were randomly assigned to one of three experimental groups with each group recalling either three, six, or nine movements on a linear-slide apparatus. The subjects, while blindfolded, were presented with each movement by actively moving to a stop. Recall occurred 5 sec after the last movement to a stop on a trial. All subjects were given nine trials, each containing a different series of to-be-recalled movements. Results indicated that absolute error of recall of the three movements increased in a linear fashion. However, for six and nine movements, a bowing effect of the recall curve was noted following the fifth position. A primacy effect was more evident than was a recency effect. Accuracy of recall was a function of list length up to six movements, after which accuracy was not further impaired.     

Observer orientation and actor-observer differences in attributions for failure

In a series of two experiments, male undergraduates either operated or watched another person operate a model racecar set. Instructions varied observers' expectancies about future involvement with the task. The drivers' causal attributions for their performance were compared with those of neutral observers as well as those of involved observers who anticipated running on the track. Predictions, derived from the Jones and Nisbett framework of actor/observer differences, were that actors should make more external than internal attributions and that neutral or “passive” observers should do the opposite. Moreover, the involved or “active” observer groups were expected to display attributional patterns similar to those of the actors. These predictions were confirmed. Results are discussed in terms of information and information-processing differences between groups.     

An analysis of motor coordination components for various localization tasks

Localization abilities of subjects in three perceptual-motor tasks were considered before and after an exposure to a visual distortion. During this distortion the subject observed his hand ballistically point to an invisible but audible target while either receiving or not receiving knowledge of results (KR) concerning pointing accuracy. Also, subjects either received a 1- or a 4-sec rest period between each of 30 exposure ballistic pointing actions. The pre- and postexposure tasks involved the ability of a subject to accurately point to an occluded and stationary auditory target, to point to the straight-ahead position in space, and to indicate when a moving, auditory target was perceived as being in the straight-ahead position. For these tasks, the pre- vs. postexposure localization difference scores are referred to as the negative aftereffect, the proprioceptive shift, and the auditory shift, respectively. Wilkinson's (1971) two-component additive model (negative aftereffect = proprioceptive shift plus auditory shift) held when KR was given regardless of amount of rest between exposure pointing responses. With a 4-sec rest and no KR, the relationship between coordination components was nonadditive (negative aftereffect greater than proprioceptive shift plus auditory shift).     

Bilateral electrodermal activity in waking man

Skin conductance responses were examined bilaterally in a group of 14 normal subjects. Twelve of them were right-handed and two were left-handed. All right-handed subjects exhibited asymmetry in skin conductance level and in skin conductance response during verbal-numerical and visual-imagery tasks. With the visual activity, larger responses were found in the left hand, while during the verbal task, larger responses were recorded from the right hand. The results were interpreted as evidence of hemispheric asymmetry of the electrodermal activity orienting response control mechanisms. More ipsilateral control for the right hand is predicted.     

Reinforcing fluency in stutterers: An experimental study

Subject-specific periods of fluent reading responses of three adult stutterers were positively reinforced with the presentation of a dime. Subjects were run individually through a sequence of two base rate, two experimental, and two extinction sessions, each session lasting 45 min. Periods of fluent reading responses increased during the experimental condition for each of the three subjects. When the reinforcer was withdrawn during the extinction condition, the frequency of fluent periods showed a decrease. Concomitantly, disfluencies decreased during the experimental condition and they increased during the extinction condition. The clinical implications of fluency manipulation as against disfluency manipulation are discussed.