A mass‐conservative staggered immersed boundary model for solving the shallow water equations on complex geometries

In this work, an approach is proposed for solving the 3D shallow water equations with embedded boundaries that are not aligned with the underlying horizontal Cartesian grid. A hybrid cut‐cell/ghost‐cell method is used together with a direction‐splitting implicit solver: Ghost cells are used for the momentum equations in order to prescribe the correct boundary condition at the immersed boundary, while cut cells are used in the continuity equation in order to conserve mass. The resulting scheme is robust, does not suffer any time step limitation for small cut cells, and conserves fluid mass up to machine precision. Moreover, the solver displays a second‐order spatial accuracy, both globally and locally. Comparisons with analytical solutions and reference numerical solutions on curvilinear grids confirm the quality of the method. Copyright © 2015 John Wiley & Sons, Ltd.     

Norchlorotestosterone Acetate: An Alternative Metabolism Study and GC–MS<Superscript>2</Superscript> Analysis in Kidney Fat,Urine, and Faeces

Norchlorotestosterone acetate (NClTA) is an anabolic steroid which resembles chlorotestosterone acetate. It cannot yet be detected by routine methods used for anabolic steroids, because there is no knowledge of its metabolic pathway. The invertebrate Neomysis integer has been used as an alternative model to study the metabolism of NClTA. The experimental results indicated the presence of 4-norchloroandrost-4-ene-17-ol-3-one (NClT) and 4-norchloroandrost-4-ene-3,17-dione (NorClAD) as possible metabolites of NClTA. Subsequently NClTA and the synthesised metabolites NClT and NorClAD were incorporated into the routine multi-residue method for detection of anabolic steroids in kidney fat, urine, and faeces.     

PHOTOMORPHOGENETIC REACTIONS and THEIR RELATION TO TIME*

Abstract— Hook-opening and leaf expansion were selected as a measure of the photoactivity of etiolated Phaseolus vulgaris L. seedlings. The experimental procedure consisted of a standard red illumination, followed by a 24-h reaction period. The magnitude of both morphogenic responses was dependent upon the time of day when the light pulse was given. The photoactivity of the etiolated seedlings changed rhythmically with a periodicity of about 6 h.     

CIRCANNUAL COURSE OF PHOTOMORPHOGENETIC REACTIVITY IN ETIOLATED BEAN SEEDLINGS

Hook opening and leaf expansion, measured 24 h after standard red light illumination, were considered as parameters determining the photoactivity of etiolated Phaseolus vulgaris L. seedlings. The experiment was repeated every h during one 17-h period each month for 1 year. The mean values for each experimental period indicated that the photoactivity of the etiolated seedlings changed markedly throughout the year according to a seasonal pattern.