9 research outputs found

    Pennsylvania Folklife Vol. 27, Folk Festival Supplement

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    • Hex Signs: A Living Tradition • Decoys and How to Make Them • Kutztown\u27s Plain People • The Old Country Kitchen: Where Food Preparation was an Art • Wooden Toys, Games and Puzzles: The Delight of All Children • A Sketch of the Seminar Stage Programs • Festival Focus • Folk Festival Programs • The Furniture-Makers at the Kutztown Festival • The Muzzle-Loading Gunsmith • Those Rare Things Called Antiques! • Mouth-Watering Baked Goods, Fresh From the Ovens! • The Art of the Potterhttps://digitalcommons.ursinus.edu/pafolklifemag/1079/thumbnail.jp

    Mass of the Southern Black Hole in NGC 6240 from Laser Guide Star Adaptive Optics

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    NGC 6240 is a pair of colliding disk galaxies, each with a black hole in its core. We have used laser guide star adaptive optics on the Keck II telescope to obtain high-resolution (0.06\sim 0.06") near-infrared integral-field spectra of the region surrounding the supermassive black hole in the south nucleus of this galaxy merger. We use the K-band CO absorption bandheads to trace stellar kinematics. We obtain a spatial resolution of about 20 pc and thus directly resolve the sphere of gravitational influence of the massive black hole. We explore two different methods to measure the black hole mass. Using a Jeans Axisymmetric Multi-Gaussian mass model, we investigate the limit that a relaxed mass distribution produces all of the measured velocity dispersion, and find an upper limit on the black hole mass at 2.0 \pm 0.2 \times 10^9 M_{\sun}. When assuming the young stars whose spectra we observe remain in a thin disk, we compare Keplerian velocity fields to the measured two-dimensional velocity field measured and fit for a mass profile containing a black hole point mass plus a radially-varying spherical component, which suggests a lower limit for the black hole mass of 8.7 \pm 0.3 \times 10^8 M_{\sun}. Our measurements of the stellar velocity dispersion place this AGN within the scatter of the MBHM_{BH}-σ\sigma_{*} relation. As NGC 6240 is a merging system, this may indicate that the relation is preserved during a merger at least until the final coalescence of the two nuclei.Comment: 10 pages, 12 figures; accepted to Ap

    Explaining Gender-Specific Racial Differences in Obesity Using Biased Self-Reports of Food Intake

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    Policymakers have an interest in identifying the differences in behavior patterns - namely, habitual caloric intake and physical activity levels - that contribute to demographic variation in body mass index (BMI) and obesity risk. While disparities in mean BMI and obesity rates between whites (non-Hispanic) and African-Americans (non-Hispanic) are well-documented, the behavioral differences that underlie these gaps have not been carefully identified. Moreover, the female-specificity of the black-white obesity gap has received relatively little attention. In the National Health and Nutrition Examination Surveys (NHANES) data, we initially observe a very weak relationship between self-reported measures of caloric intake and physical activity and either BMI or obesity risk, and these behaviors appear to explain only a small fraction of the black-white BMI gap (or obesity gap) among women. These unadjusted estimates echo previous findings from large survey datasets such as the NHANES. Using an innovative method to mitigate the widely recognized problem of measurement error in self-reported behaviors' proxying for measurement errors using the ratio of reported caloric intake to estimated true caloric needs' we obtain much stronger relationships between behaviors and BMI (or obesity risk). Behaviors can in fact account for a significant share of the BMI gap (and the obesity gap) between black women and white women and are consistent with the presence of much smaller gaps between black men and white men. The analysis also shows that the effects smoking has on BMI and obesity risk are small-to-negligible when measurement error is properly controlled

    Rationale, design and methods for a staggered-entry, waitlist controlled clinical trial of the impact of a community-based, family-centred, multidisciplinary program focussed on activity, food and attitude habits (Curtin Universitys activity, food and att

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    Background: Current estimates place just under one quarter of adolescents in Australia as overweight or obese. Adolescence has been identified as a critical period for the development of obesity, yet despite this recognition, there is limited systematic research into or evaluation of interventions for overweight adolescents. Reviews have concluded that there is a substantive evidence gap for effective intervention, but physical activity, lifestyle change and family involvement have been identified as promising foci for treatment. Methods: This paper reports on the development of a staggered-entry, waitlist controlled clinical trial to assess the impact of a multidisciplinary intervention aiming to change the poor health trajectory of overweight adolescents and help them avoid morbid obesity in adulthoodCurtin Universitys Activity, Food and Attitudes Program (CAFAP). 96 adolescents, aged 1116 years, and parents, will attend twice weekly during an 8 week intensive multidisciplinary program with maintenance follow-up focussed on improving activity, food and attitude habits. Follow-up assessments will be conducted immediately after completing the intensive program, and at 3, 6 and 12 months post intensive program. Main outcomes will be objectively-measured physical activity, sedentary behaviour and activity behaviours; food intake (measured by 3 day diary) and food behaviours; body composition, fitness and physical function; mental and social well-being (quality of life, mood and attitudes), and family functioning. Discussion: This trial will provide important information to understand whether a community based multidisciplinary intervention can have short and medium term effects on activity and food habits, attitudes, and physical and mental health status of overweight adolescents. Trial registration: Australian New Zealand Clinical Trials Registry ACTRN12611001187932
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