Correlates of Body Image of Undergraduate Females Attending Andrews University

Problem: Literature on the relationship between ethnic identity and body image has been scarce, focusing almost entirely on the Asian and/or Hispanic population. The purpose of this study is to examine the influence that ethnic identity has on the body image of undergraduate females. Method: In the present study, I explored the extent to which body image is related to ethnicity in a diverse sample of 345 undergraduate females (43.5% Caucasian American, 17.4% African American, 9.3% West Indian/Caribbean, 14.8% Hispanic American, 12.5%, Asian American, & 2.6% Multi-ethnic) from a Seventh-day Adventist university. Possible correlates of body dissatisfaction such as ethnic identity, religious commitment, sociocultural pressure, and internalization of the thinness ideal were also explored. Results: Results of this study indicated that low ratings on Sociocultural Pressure and Internalization of the Thinness Ideal were related to positive body image perceptions. As a whole, undergraduate females in this study presented with a positive body image. Specifically, the women expressed positive feelings about their bodies, had lower preoccupation with their weight, classified their weight as normal, and were moderately satisfied with all areas of their body. In terms of ethnic identity, the females in this study had low interest and little awareness of their own ethnicity. As seen in previous research, the only significant correlates of body image that emerged in this study were sociocultural pressure and internalization of the thinness ideal. Conclusions: Body image concerns of undergraduate females may not be as prevalent as once thought. Females are displaying greater body satisfaction than in the recent past. Differences in body dissatisfaction among the Seventh-day Adventist sample including various ethnic groups are becoming non-existent. This may be due to the Seventh-day Adventist culture serving as a protective factor against body image dissatisfaction. Another possible explanation is the increased emphasis on social media

Comparison of bipyridyl, maltol and kojic acid action as organic vanadium ligands on activity of galactosyltransferase (EC 2.4.1.38), some physiological parameters and ultrastructure of Golgi complexes in rat hepatocytes.

The biochemical activity and morphology of control and streptozotocin-diabetic rat liver Golgi complexes were previously investigated by us under influence of some vanadium [V(IV)] compounds. The effectiveness of these derivatives depends on the kind of complexing ligands. This paper presents the investigation of the effect of bipyridyl, the ligand of a new vanadium compound, tested by us with maltol and kojic acid (two ligands studied by the present and other authors). The three ligands alone action was tested under the same experimental conditions as in the case of whole compounds with vanadium and applied to liver Golgi complexes of control rats. A preliminary study for maltol and kojic acid had been previously carried out by us parallel with tests of whole vanadium complexes, but valuable differences in biological action found in our condition of experiments suggested the extension of studies to include the two above-mentioned ligands and to compare the effects of the three investigated ligands. The supplementary part of the experiment focused mainly on the ultrastructure of Golgi complexes in hepatocytes. Four groups of animals were used: C - control rats, C + M (maltol), C + (ka)2 (kojic acid) and C + (bpy)2 (bipyridyl). The control rats received 0.09M NaCl as drinking liquid; all the other animals were given 3.6 mmol/L of appropriate ligand solution in 0.09M NaCl during 7 days. All the animals survived the experiments. Only in group C + (bpy)2 did the authors observe statistically significant differences as compared with the controls (group C). The differences were detected in physiological studies and manifested as body weight decreased by approximately 20% during the experiment, lower liquid (

Compositional and textural analysis of host-rock diamictite matrix at the Kakula copper deposit, Democratic Republic of Congo

The Kakula deposit is a high-grade sedimentary-rock-hosted Cu deposit (628 Mt, 2.72% Cu indicated resource, 1% cut-off) ~10 km south of the Kamoa deposit (759 Mt, 2.57% Cu indicated resource, 1% cut-off) in the central African copperbelt, Democratic Republic of Congo. Copper-sulphide ore (chalcocite, bornite, chalcopyrite) at Kakula is predominantly disseminated in the fine-grained matrix of clast-poor (≤20% clasts ≥2 mm) subaqueous debrite (diamictite), at the base of the nearly flat-lying midNeoproterozoic “grand conglomérat” (Mwale formation). Scanning electron microscopy was used to document matrix texture and composition to develop a matrix paragenesis, recorded in five phases of the matrix evolution: sedimentation, pre-ore diagenesis, mainore mineralisation, post-ore alteration, and weak tectonism. The ore-zone matrix is porous, up to 12.5%, and consists of clay- to silt-sized muscovite, quartz, chlorite, Kfeldspar, dolomite, and biotite, whereas least-altered matrix, several hundred metres above copper-sulphide mineralisation, consists of clay- to silt-sized quartz, albite, chlorite, K-feldspar, calcite, and dolomite. Copper-sulphide precipitation is contemporaneous with chlorite and biotite (+/- hematite, quartz, and K-feldspar) and fit in a paragenetic sequence between diagenetic pyrite (± Fe-dolomite) and later muscovite. Hematite is ore-stage and most abundant in areas containing chalcocite. Areas of mm- to cm-scale “aligned” matrix (nearly vertical microfabric of aligned, elongated grains) consists of a higher abundance of muscovite, locally elongated copper-sulphides, and a lower concentration of copper than non-aligned matrix, suggesting that copper-sulphide development pre-dated fabric development and that copper-sulphide grains were later dissolved and possibly remobilised. Although determining the original mineralogy and texture of the diamictite matrix is challenging, the depositional matrix characteristics (clast-rich versus clast-poor diamictite) and the availability of reactive agents (e.g., diagenetic pyrite) may have been important controls on copper grade and distribution. More work is required to constrain the absolute timing of mineralisation, which is a major debate at Kakula and Kamoa.Master of Science (MSc) in Geolog

1,4-Diazo­niabicyclo­[2.2.2]octane bis­(2,4,6-trinitro­phenolate)

In the title compound, C6H14N2 2+·2C6H2N3O7 −, the cation possesses crystallographically imposed twofold rotation symmetry. In the crystal structure, the cation and anions are linked into a trimeric aggregate by inter­molecular N—H⋯O hydrogen bonds. The trimeric units are further connected by π–π inter­actions [centroid–centroid distances = 3.507 (2)–3.660 (3) Å], forming layers parallel to the bc plane

Materials science at Swiss universities of applied sciences

Copyright ©Swiss Chemical Society: CHIMIA, Volume 73, Numbers 7-8, August 2019, pp. 645-655(11)In the Swiss Universities of Applied Sciences, several research institutes are involved in Materials Science, with different approaches and applications fields. A few examples of recent projects from different groups of the University of Applied Sciences and Arts Western Switzerland (HES-SO), the Zurich University of Applied Sciences (ZHAW) and the University of Applied Sciences and Arts Northwestern Switzerland (FHNW) are given

Novel strategy for the calorimetry-based control of fed-batch cultivations of saccharomyces cerevisiae

Typical controllers for fed-batch cultivations are based on the estimation and control of the specific growth rate in real time. Biocalorimetry allows one to measure a heat signal proportional to the substrate consumed by cells. The derivative of this heat signal is usually used to evaluate the specific growth rate, introducing noise to the resulting estimate. To avoid this, this study investigated a novel controller based directly on the heat signal. Time trajectories of the heat signal setpoint were modelled for different specific growth rates, and the controller was set to follow this dynamic setpoint. The developed controller successfully followed the setpoint during aerobic cultivations of Saccharomyces cerevisiae, preventing the Crabtree effect by maintaining low glucose concentrations. With this new method, fed-batch cultivations of S. cerevisiae could be reliably controlled at specific growth rates between 0.075 h−1 and 0.20 h−1, with average root mean square errors of 15 ± 3%

Cole-Cole, linear and multivariate modeling of capacitance data for on-line monitoring of biomass

This work evaluates three techniques of calibrating capacitance (dielectric) spectrometers used for on-line monitoring of biomass: modeling of cell properties using the theoretical Cole-Cole equation, linear regression of dual-frequency capacitance measurements on biomass concentration, and multivariate (PLS) modeling of scanning dielectric spectra. The performance and robustness of each technique is assessed during a sequence of validation batches in two experimental settings of differing signal noise. In more noisy conditions, the Cole-Cole model had significantly higher biomass concentration prediction errors than the linear and multivariate models. The PLS model was the most robust in handling signal noise. In less noisy conditions, the three models performed similarly. Estimates of the mean cell size were done additionally using the Cole-Cole and PLS models, the latter technique giving more satisfactory result

The Influence of Active Phase Loading on the Hydrodeoxygenation (HDO) of Ethylene Glycol over Promoted MoS2_{2}/MgAl2_{2}O4_{4} Catalysts

The hydrodeoxygenation (HDO) of ethylene glycol over MgAl$_{2}$O$_{4}$ supported NiMo and CoMo catalysts with around 0.8 and 3 wt% Mo loading was studied in a continuous flow reactor setup operated at 27 bar H$_{2}$ and 400 °C. A co-feed of H2S of typically 550 ppm was beneficial for both deoxygenation and hydrogenation and for enhancing catalyst stability. With 2.8-3.3 wt% Mo, a total carbon based gas yield of 80-100 % was obtained with an ethane yield of 36-50 % at up to 118 h on stream. No ethylene was detected. A moderate selectivity towards HDO was obtained, but cracking and HDO were generally catalyzed to the same extent by the active phase. Thus, the C2/C1 ratio of gaseous products was 1.1-1.5 for all prepared catalysts independent on Mo loading (0.8-3.3 wt%), but higher yields of C1-C3 gas products were obtained with higher loading catalysts. Similar activities were obtained from Ni and Co promoted catalysts. For the low loading catalysts (0.83-0.88 wt% Mo), a slightly higher hydrogenation activity was observed over NiMo compared to CoMo, giving a relatively higher yield of ethane compared to ethylene. Addition of 30 wt% water to the ethylene glycol feed did not result in significant deactivation. Instead, the main source of deactivation was carbon deposition, which was favored at limited hydrogenation activity and thus, was more severe for the low loading catalysts