Sex differences in reinforcement and punishment on prime-time television

Prime-time television programs were analyzed for frequencies of positive reinforcement and punishment exchanged among performers varying in age and sex. Results indicated that most responses were given by and directed to adult males. Moreover, while adult males exhibited and received similar frequencies of reinforcement and punishment, adult females were likely to give and to be the recipients of more reinforcement than punishment. Proportional analyses which controlled for sex differences in frequencies of responses revealed that females more often exhibited and received reinforcement, whereas males more often exhibited and received punishment. Results are interpreted from a social learning theory perspective and the implications for children's learning of positive and negative behaviors are explored.     

Ethical issues in diagnosis

The ways in which ethical issues arise in making clinical judgments are briefly discussed. By showing the topography of the role of value judgments in medical diagnostics it is suggested why clinical medicine remains inextricably a value-infected science.     

New perspectives in temperament/personality research: The “Behavioral” model of the Warsaw group

This paper reviews the theory and research of the Warsaw school of differential psychophysiology, which has modified and extended the typologic model constructed by Teplov and Nebylitsyn. While Soviet theory still favors a relatively inflexible structure of nervous system properties as the biologic basis of individual differences in personality, Strelau and colleagues, in line with the action/activity model of Vygotsky and Tomaszewski, begin with the premise that for every individual there is a specific, genetically determined optimal level of arousal, a necessary background for fullest emotional and intellectual development. The person strives to create this optimal climate through an active process of stimulation control, achieved primarily through enhancement or dampening of reactivity—which describes innate responsivity in the reacting systems to both sensory and emotional stimuli—through various hormonal ‘tuning’ mechanisms and through “appropriate” activity, reflected in different cognitive styles and preference for certain work conditions. Such activities aim to ensure comfortable physical and psychologic environments, in which the individual can avoid conflict and stress. The system regulating and integrating such control mechanisms is the core of personality. Investigations of the Warsaw group on relationships between reactivity and different forms of stimulation seeking/control—risk-taking, work style preferences, cognitive style, defense mechanisms, for example—and between reactivity and tolerance of stress and conflict and their speculations about the neurophysiologic and endocrinologic mechanisms of stimulation control are described, as are a number of questionnaires developed by this group to measure reactivity, the temporal parameters of response, and stimulation-seeking in a variety of occupational and social contexts.     

Two auditory aftereffects and their dependency on carrier frequency

It is suggested that aftereffects caused by swept change of sound level (Reinhardt-Rutland & Anstis, Note 1) may contribute to auditory motion aftereffects (Grantham & Wightman, 1979). The latter appear to show selectivity for frequency; they are substantial if the frequency is .5 kHz but not if it is 2 kHz. An experiment was carried out to show to what extent there is such selectivity for aftereffects from swept sound-level change; this showed that they are substantial over a much wider range of frequencies than auditory motion aftereffects. It is concluded that the frequency selectivity of auditory motion aftereffects might be explained by frequency selectivity for inter-aural phase differences.     

Saltation through the blind spot

At least three localization illusions can be produced by varying the time relations between two stimuli. Two of these, phi motion and Békésy’s illusion, have been induced in areas lacking receptors. To learn if this also occurred with the third illusion, sensory saltation, people reported their observations when Geldard’s visual rabbit was induced by stimulating points around the optic disk. The rabbit crossed the blind spot as well as other portions of the eyes, and the illusory point was often localized within the region of the blind spot. All three illusions can be localized in an area devoid of receptors.     

Effective luminance contrast as a parameter in contingent aftereffects

Variation in the magnitude of contingent aftereffects was explored as a function of the luminance contrast ratio profile of inspection stimuli. Positive contrast stimuli (chromatic bars interspersed with achromatically brighter bars) produced substantially attenuated aftereffects compared with negative contrast stimuli (chromatic and dark bars). This attenuation was hypothesized to result from retinal image deterioration of positive contrast gratings due to retinal reflection/scatter. In a second experiment, subjects selected for their light retinal pigmentation manifested substantial enhancement of the asymmetry between the aftereffects generated by positive and negative contrast gratings. Those with dark fundus pigmentation showed symmetrical aftereffects.     

Functional Differences Between Upright and Rotated Images

In Experiment I subjects imaged an alphanumeric character either upright or upside-down, and triggered a test display character. Their task was to decide as quickly as possible whether the test character was NORMAL or MIRRORED. On 72% of the trials the test was at the orientation imaged. Reaction time (RT) was then about 200 ms longer in the upside-down image condition. This difference reduced with practice. On the remaining trials the orientation of the test character differed from that of the prepared image. For upright images RT increased monotonically with the angular difference in orientation between test and image. For upside-down images RT did not increase monotonically with angular difference as there was a wide dip around the upright. Further experiments suggested that upside-down images can be rotated, but at considerably slower rates than upright ones, and that the apparent rates of rotation for upside-down images are dependent upon the width of the sector tested. These results indicate that visual short-term memory (STM) and long-term memory (LTM) are distinct; that the process of mental rotation does not operate directly upon LTM; and that functionally, upright and rotated images may differ in important ways.