High blushing propensity: fearful preoccupation or facial coloration?

Twenty-seven women with high scores on the Blushing Propensity Scale (BPS) and 26 women with low BPS scores were exposed to two different video segments. One video showed the subject's own singing, recorded in a previous session and the other video showed a segment of Hitchcock's movie Psycho. During the experiment, facial coloration, facial temperature, and skin conductance level were measured. In addition, subjects' blushing intensity was judged by raters. Finally, subjects were asked to rate their blushing intensity and fear of blushing during the video presentations. Subjects generally blushed more during the presentation of their singing than during comparison stimulation, as measured physiologically. There were no between group differences in this respect. No differences were found between the two groups on raters' judgements about blushing intensity. However, high BPS subjects dramatically overestimated their blushing intensity and were more afraid of blushing than low BPS subjects. During the mere presence of the raters, high BPS subjects tended to show a relatively strong coloration. Thus, the BPS seems to reflect both a fearful preoccupation and a stronger facial coloration.     

Binocular rivalry with moving patterns

Binocular rivalry between a horizontal and a vertical grating was examined in six experiments. The gratings could be presented in a static form or dynamically so that either one or both gratings moved. The motion consisted of a symmetrical transformation of the gratings about their centers, so that the lines moved outwards or inwards. During rivalry, a moving pattern was visible for about 50% longer than an equivalently oriented static pattern (Experiments 1, 2, and 4). When both gratings were in motion (Experiments 3 and 5), the course of rivalry was similar to that found for two static gratings. The duration of dominance of the moving grating was influenced by its velocity (Experiment 6). The results are interpreted in terms of the stimulus strengths of the static and dynamic patterns.     

The estimation of ultrametric and path length trees from rectangular proximity data

A least-squares algorithm for fitting ultrametric and path length or additive trees to two-way, two-mode proximity data is presented. The algorithm utilizes a penalty function to enforce the ultrametric inequality generalized for asymmetric, and generally rectangular (rather than square) proximity matrices in estimating an ultrametric tree. This stage is used in an alternating least-squares fashion with closed-form formulas for estimating path length constants for deriving path length trees. The algorithm is evaluated via two Monte Carlo studies. Examples of fitting ultrametric and path length trees are presented.G. De Soete is Aspirant of the Belgian Nationaal Fonds voor Wetenschappelijk Onderzoek at the University of Ghent, Belgium. W. S. DeSarbo and J. D. Carroll are Members of Technical Staff at AT&T Bell Laboratories, Murray Hill, N.J. G. W. Furnas is Member of Technical Staff at Bell Communications Research, Murray Hill, N.J.     

Frequency versus magnitude of reinforcement: New data with a different procedure

Two pigeons, with previous exposure to concurrent schedules, were submitted to 29 sessions of 8 hours each with concurrent variable-interval variable-interval schedules in which reinforcement parameters changed from session to session. In the first nine sessions reinforcement durations were equal in both schedules while reinforcement frequencies varied; in Sessions 10 through 18, both frequency and duration of reinforcement were varied; in Sessions 19 through 29, only reinforcement duration was varied. Results with this different procedure confirm previous findings that behavior is more sensitive to changes in reinforcement frequency than to reinforcement magnitude.     

Upper bounds for Kruskal's stress

In this paper the relationships between the two formulas for stress proposed by Kruskal in 1964 are studied. It is shown that stress formula one has a system of nontrivial upper bounds. It seems likely that minimization of this loss function will be liable to produce solutions for which this upper bound is small. These are regularly shaped configurations. Even though stress formula two yields less equivocal results, it seems to be expected that minimization of this loss function will tend to produce configurations in which the points are clumped. These results give no clue as to which of the two loss functions is to be preferred.This study has been supported by the Nederlandse Organisatie voor Zuiver-Wetenschappelijk Onderzoek (Netherlands Organization for the Advancement of Pure Research), under grant 56-146.Comments by Willem Heiser and Frank Critichley have been very helpful.The second author presently is employed by the Netherlands Central Bureau of Statistics, Voorburg.     

Anxiety, perception, and control of heart rate

8 women and 8 men took Cattell's IPAT-anxiety questionnaire and later McFarland's test of ability to perceive heart activity. The second test involved subjects' tracking their own heart rates, then they enrolled in an EKG biofeedback session to evaluate ability to increase and decrease heart rate from subjects' resting baselines. At the end of the session each subject completed Blanchard, et al.'s questionnaire to specify the cognitive strategies used for heart-rate control. Heart rate, abdominal respiration rate, respiration amplitude, EEG percent power in theta, alpha, and beta bands were evaluated. Success of heart-rate decrease seemed to depend mainly on activity levels: the subjects who achieved high scores on the activity test decreased heart rate significantly better than did low scorers. The relationship between scores for perception of heart and increases in heart rate was nonsignificant: increased heart-rate seemed to depend on differences in respiration between the rest and periods of increase. The significant, negative correlation between trait anxiety and perceptions of heart activity suggested that anxiety affected subjects' ability to perceive heart rate. The theta EEG power of the right hemisphere was significantly higher in subjects scoring high than for those low in perception of heart activity. During heart-rate increase tasks subjects mainly reported use of 'arousal responses,' similarly during heart-rate decrease tasks they reported use of relaxation responses.     

Dyslexia: saccadic eye movements

This paper describes an extensive study of the parameters of saccadic eye movement in a group of 28 poor-reading children and a comparative normally reading group of 31 children. Ages ranged from 6.0 to 16.9 yr. Poor readers had normal intelligence but were lagging by at least two years in reading ability as compared to their peer age group. Parameters studied in refixation eye movements included saccadic latency, accuracy, velocity, and acceleration, as well as differences in latency for abduct and adduct movements. Shapes of saccades were also studied. It was shown that eye-movement performance in simple saccadic refixation was not distinguishably different for poor readers and normal readers, even though in reading, which requires higher processing, eye-movement characteristics are quite different. Maturational changes for various saccadic eye-movement parameters were also examined for the normal and poor reading groups.     

Dynamic balance of learning disabled and nondisabled children

This investigation assessed a difference in the dynamic balance abilities of 30 learning disabled and 30 nondisabled children of elementary-school age. Only distance traveled across the beam, a novel task, was significantly different between groups; no other effects were significant. Nondisabled subjects traveled further across the beam before losing balance than learning disabled children.