Teaching business ethics: Plato was right

Ethical lapses in major corporations continue to draw public attention to the specter of corporate misconduct. This paper presents a pedagogical approach that is designed to enhance student understanding and appreciation of the challenges that business leaders face when confronted with the conflict between the profit-maximizing demands of capitalism and the ethical expectations of society. This is an approach that fully acknowledges the seductive nature of unethical conduct in search of corporate rewards. This paper presents a method which can be applied both in undergraduate and graduate coursework, facilitates the examination of two corruption cases (Enron and WorldCom), and highlights short-term gain versus the eventual long-term pain of unethical behavior

The Acute and Residual Effect of a Single Exercise Session on Meal Glucose Tolerance in Sedentary Young Adults

The study goals were to (1) establish the variability in postprandial glucose control in healthy young people consuming a mixed meal and, then (2) determine the acute and residual impact of a single exercise bout on postprandial glucose control. In study 1, 18 people completed two similar mixed meal trials and an intravenous glucose tolerance test (IVGTT). There were strong test-retest correlations for the post-meal area under the curve (AUC) for glucose, insulin, and Cpeptide (r = 0.73–0.83) and the Matsuda insulin sensitivity index (ISI, r = 0.76), and between meal and IVGTT-derived ISI (r = 0.83). In study 2, 11 untrained young adults completed 3 trials. One trial (No Ex) was completed after refraining from vigorous activity for ≥3 days. On the other 2 trials, a 45-min aerobic exercise bout was performed either 17-hours (Prior Day Ex) or 1-hour (Same Day Ex) before consuming the test meal. Compared to No Ex and Prior Day Ex, which did not differ from one another, there were lower AUCs on the Same Day Ex trial for glucose (6%), insulin (20%) and C-peptide (14%). Thus, a single moderate intensity exercise session can acutely improve glycemic control but the effect is modest and short-lived

Wind tunnel model surface gauge for measuring roughness

The optical inspection of surface roughness research has proceeded along two different lines. First, research into a quantitative understanding of light scattering from metal surfaces and into the appropriate models to describe the surfaces themselves. Second, the development of a practical instrument for the measurement of rms roughness of high performance wind tunnel models with smooth finishes. The research is summarized, with emphasis on the second avenue of research

Comparative studies of the scanning tunneling spectra in cuprate and iron-arsenide superconductors

We report scanning tunneling spectroscopic studies of cuprate and iron-arsenic superconductors, including YBa_2Cu_3O_{7-\delta} (Y-123, T_c = 93 K), Sr_{0.9}La_{0.1}CuO_2 (La-112, T_c = 43 K), and the "122" compounds Ba(Fe_{1-x}Co_x)_2As_2 (Co-122 with x = 0.06, 0.08, 0.12 for T_c = 14, 24, 20 K). For H > 0, pseudogap (\Delta_{PG}) features are revealed inside the vortices, with \Delta_{PG} = [(\Delta_{eff})^2+(\Delta_{SC})^2]^{1/2} > \Delta_{SC} in Y-123 and \Delta_{PG} < \Delta_{SC} in La-112, suggesting that the physical origin of \Delta_{PG} is a competing order coexisting with superconductivity. Additionally, Fourier transformation (FT) of the Y-123 spectra exhibits two types of spectral peaks, one type is associated with energy (\omega)-dependent quasiparticle interference (QPI) wave-vectors and the other consists of \omega-independent wave-vectors due to competing orders and (\pi,\pi) magnetic resonances. For the multi-band Co-122 compounds, two-gap superconductivity is found for all doping levels. Magnetic resonant modes that follow the temperature dependence of the superconducting gaps are also identified. These findings, together with the \omega- and x-dependent QPI spectra, are consistent with a sign-changing s-wave pairing symmetry in the Co-122 iron arsenides. Our comparative studies suggest that the commonalities among the cuprate and the ferrous superconductors include the proximity to competing orders, antiferromagnetic (AFM) spin fluctuations and magnetic resonances in the superconducting (SC) state, and the unconventional pairing symmetries with sign-changing order parameters on different parts of the Fermi surface.Comment: 6 pages, 3 figures. Submitted to Journal of Physics: Conference Proceedings for the 26th International Low-Temperature Conference (2011). Corresponding author: Nai-Chang Yeh ([email protected]

HSD3B1 genotype identifies glucocorticoid responsiveness in severe asthma

Asthma resistance to glucocorticoid treatment is a major health problem with unclear etiology. Glucocorticoids inhibit adrenal androgen production. However, androgens have potential benefits in asthma. HSD3B1 encodes for 3β-hydroxysteroid dehydrogenase-1 (3β-HSD1), which catalyzes peripheral conversion from adrenal dehydroepiandrosterone (DHEA) to potent androgens and has a germline missense-encoding polymorphism. The adrenal restrictive HSD3B1(1245A) allele limits conversion, whereas the adrenal permissive HSD3B1(1245C) allele increases DHEA metabolism to potent androgens. In the Severe Asthma Research Program (SARP) III cohort, we determined the association between DHEA-sulfate and percentage predicted forced expiratory volume in 1 s (FEV1PP). HSD3B1(1245) genotypes were assessed, and association between adrenal restrictive and adrenal permissive alleles and FEV1PP in patients with (GC) and without (noGC) daily oral glucocorticoid treatment was determined (n = 318). Validation was performed in a second cohort (SARP I&II; n = 184). DHEA-sulfate is associated with FEV1PP and is suppressed with GC treatment. GC patients homozygous for the adrenal restrictive genotype have lower FEV1PP compared with noGC patients (54.3% vs. 75.1%; P < 0.001). In patients with the homozygous adrenal permissive genotype, there was no FEV1PP difference in GC vs. noGC patients (73.4% vs. 78.9%; P = 0.39). Results were independently confirmed: FEV1PP for homozygous adrenal restrictive genotype in GC vs. noGC is 49.8 vs. 63.4 (P < 0.001), and for homozygous adrenal permissive genotype, it is 66.7 vs. 67.7 (P = 0.92). The adrenal restrictive HSD3B1(1245) genotype is associated with GC resistance. This effect appears to be driven by GC suppression of 3β-HSD1 substrate. Our results suggest opportunities for prediction of GC resistance and pharmacologic intervention

1983: Abilene Christian College Bible Lectures - Full Text

LIGHTS IN A WORLD OF DARKNESS Being the Abilene Christian University Annual Bible Lectures 1983 Published by Abilene Christian University Book Store ACU Station Abilene, Texas 7969

Dynamical masses and stellar evolutionary model predictions of M stars

Funding: J.P. gratefully acknowledges the support of the National Science Foundation (NSF) Graduate Research Fellowship through grant Nos. DGE1144152 and DGE1745303. K.I.Ö. gratefully acknowledges the support of the Simons Foundation through a Simons Collaboration on the Origins of Life (SCOL) PI grant (No. 321183). G.J.H. is supported by general grant 11773002 awarded by the National Science Foundation of China. L.I.C. gratefully acknowledges support from the David and Lucille Packard Foundation, the Virginia Space Grant Consortium, and Johnson & Johnson’s WiSTEM2D Award. V.V.G. gratefully acknowledges support from FONDECYT Iniciación 11180904. Support for this work was also provided by NASA through the NASA Hubble Fellowship grant Nos. HST-HF2-51460.001-A, HST-HF2-51405.001-A, and HST-HF2-51429.001-A awarded by the Space Telescope Science Institute, which is operated by the Association of Universities for Research in Astronomy, Inc., for NASA, under contract NAS5-26555.In this era of Gaia and ALMA, dynamical stellar mass measurements, derived from spatially and spectrally resolved observations of the Keplerian rotation of circumstellar disks, provide benchmarks that are independent of observations of stellar characteristics and their uncertainties. These benchmarks can then be used to validate and improve stellar evolutionary models, the latter of which can lead to both imprecise and inaccurate mass predictions for pre-main-sequence, low-mass (≤0.5 M⊙) stars. We present the dynamical stellar masses derived from disks around three M stars (FP Tau, J0432+1827, and J1100-7619) using ALMA observations of 12CO (J = 2-1) and 13CO (J = 2-1) emission. These are the first dynamical stellar mass measurements for J0432+1827 and J1100-7619 (0.192 ± 0.005 M⊙ and 0.461 ± 0.057 M⊙, respectively) and the most precise measurement for FP Tau (0.395 ± 0.012 M⊙). Fiducial stellar evolutionary model tracks, which do not include any treatment of magnetic activity, agree with the dynamical stellar mass measurement of J0432+1827 but underpredict the mass by ∼60% for FP Tau and by ∼80% for J1100-7619. Possible explanations for the underpredictions include inaccurate assumptions of stellar effective temperature, undetected binarity for J1100-7619, and that fiducial stellar evolutionary models are not complex enough to represent these stars. In the former case, the stellar effective temperatures would need to be increased by amounts ranging from ∼40 to ∼340 K to reconcile the fiducial stellar evolutionary model predictions with the dynamically measured masses. In the latter case, we show that the dynamical masses can be reproduced using results from stellar evolutionary models with starspots, which incorporate fractional starspot coverage to represent the manifestation of magnetic activity. Folding in low-mass M stars from the literature and assuming that the stellar effective temperatures are imprecise but accurate, we find tentative evidence of a relationship between fractional starspot coverage and observed effective temperature for these young, cool stars.Publisher PDFPeer reviewe

Escherichia coli-mediated impairment of ureteric contractility is uropathogenic E. coli specific.

BACKGROUND: Ureters are fundamental for keeping kidneys free from uropathogenic Escherichia coli (UPEC), but we have shown that 2 strains (J96 and 536) can subvert this role and reduce ureteric contractility. To determine whether this is (1) a widespread feature of UPEC, (2) exhibited only by UPEC, and (3) dependent upon type 1 fimbriae, we analyzed strains representing epidemiologically important multilocus sequence types ST131, ST73, and ST95 and non-UPEC E. coli. METHODS: Contractility and calcium transients in intact rat ureters were compared between strains. Mannose and fim mutants were used to investigate the role of type 1 fimbriae. RESULTS: Non-UPEC had no significant effect on contractility, with a mean decrease after 8 hours of 8.8%, compared with 8.8% in controls. UPEC effects on contractility were strain specific, with decreases from 9.47% to 96.7%. Mannose inhibited the effects of the most potent strains (CFT073 and UTI89) but had variable effects among other UPEC strains. Mutation and complementation studies showed that the effects of the UTI89 cystitis isolate were fimH dependent. CONCLUSIONS: We find that (1) non-UPEC do not affect ureteric contractility, (2) impairment of contractility is a common feature of UPEC, and (3) the mechanism varies between strains, but for the most potent UPEC type 1 fimbriae are involved

An Evolutionary Reduction Principle for Mutation Rates at Multiple Loci

A model of mutation rate evolution for multiple loci under arbitrary selection is analyzed. Results are obtained using techniques from Karlin (1982) that overcome the weak selection constraints needed for tractability in prior studies of multilocus event models. A multivariate form of the reduction principle is found: reduction results at individual loci combine topologically to produce a surface of mutation rate alterations that are neutral for a new modifier allele. New mutation rates survive if and only if they fall below this surface - a generalization of the hyperplane found by Zhivotovsky et al. (1994) for a multilocus recombination modifier. Increases in mutation rates at some loci may evolve if compensated for by decreases at other loci. The strength of selection on the modifier scales in proportion to the number of germline cell divisions, and increases with the number of loci affected. Loci that do not make a difference to marginal fitnesses at equilibrium are not subject to the reduction principle, and under fine tuning of mutation rates would be expected to have higher mutation rates than loci in mutation-selection balance. Other results include the nonexistence of 'viability analogous, Hardy-Weinberg' modifier polymorphisms under multiplicative mutation, and the sufficiency of average transmission rates to encapsulate the effect of modifier polymorphisms on the transmission of loci under selection. A conjecture is offered regarding situations, like recombination in the presence of mutation, that exhibit departures from the reduction principle. Constraints for tractability are: tight linkage of all loci, initial fixation at the modifier locus, and mutation distributions comprising transition probabilities of reversible Markov chains.Comment: v3: Final corrections. v2: Revised title, reworked and expanded introductory and discussion sections, added corollaries, new results on modifier polymorphisms, minor corrections. 49 pages, 64 reference