Neutron and proton transverse emission ratio measurements and the density dependence of the asymmetry term of the nuclear equation of state

Recent measurements of preequilibrium neutron and proton transverse emission from (112,124)Sn+(112,124)Sn reactions at 50 MeV/A have been completed at the National Superconducting Cyclotron Laboratory. Free nucleon transverse emission ratios are compared to those of A=3 mirror nuclei. Comparisons are made to Boltzmann-Uehling-Uhlenbeck (BUU) transport calculations and conclusions concerning the density dependence of the asymmetry term of the nuclear equation of state at subnuclear densities are made. Comparison to BUU model predictions indicate a density dependence of the asymmetry energy that is closer to a form in which the asymmetry energy increases as the square root of the density for the density region studied. A coalescent-invariant analysis is introduced as a means of reducing suggested difficulties with cluster emission in total nucleon emission.     

ZI round,a MIP rounding heuristic

We introduce a new pure integer rounding heuristic, ZI Round, and compare this heuristic to recent extremely fast pure integer rounding heuristic Simple Rounding. Simple Rounding was introduced in the non-commercial code SCIP. ZI Round attempts to round each fractional variable while using row slacks to maintain primal feasibility. We use the MIPLIB 2003 library for the test set. The average time in our run per instance for both Simple Rounding and ZI Round was 0.8 milliseconds, but ZI Round found more feasible solutions with a the same or better objective value. Also the average time to solve the lp relaxation per instance was 2.2 seconds, so these two rounding heuristics are several magnitudes faster than other heuristics which must use the lp solver, including diving heuristics. We also show that ZI Round performs well on a set covering class and a railway crew scheduling class.     

Meeting Reports: International Workshop on the Protein Circular Dichroism Data Bank

The International Workshop on the Protein Circular Dichroism Data Bank (PCDDB) was held on April 11–13, 2005, at Birkbeck College, University of London, UK, under the sponsorship of the UK Biotechnology and Biological Sciences Research Council. The meeting was chaired by Bonnie Ann Wallace, Professor in the Department of Crystallography at Birkbeck College. The workshop organizing committee consisted of Dr. Robert W. Janes, Queen Mary, University of London, and Dr. Lee Whitmore, also of Birkbeck College.

Participants included experts in both conventional circular dichroism (CD) spectroscopy and representatives from synchrotron radiation circular dichroism (SRCD) beamlines: Prof. J. Sutherland of the NSLS SRCD beamlines U9b and U11 and East Carolina University (USA);     

BioCD-2008: Synchrotron Radiation Circular Dichroism Spectroscopy of Proteins and Other Biomolecules

A weeklong workshop focusing on circular dichroism (CD) spectroscopy using both conventional and synchrotron sources (SRCD) was presented at the National Synchrotron Light Source at Brookhaven National Laboratory from June 23–27, 2008.     

Review of Experiments on the Convection of Light

The interferometric experiments on the convection of white light in flowing water first done by Fizeau in 1851 and later repeated by Michelson and Morley in 1886 are quantitatively meaningless. The work by Zeeman in 1914 on flowing water is in agreement with an incorrect formulation. His observations can also be interpreted to be in agreement with the conventional addition of speeds rather than the Einstein addition theorem. Zeeman's experiments with moving quartz rods led to ambiguous and inaccurate results. His experiments on moving glass rods are also quantitatively meaningless due to the use of white rather than monochromatic light. Experiments with a “ring” laser interferometer published in 1964 present results both in agreement and in disagreement with an incorrectly formulated prediction.     

Transition Metal‐Free Reduction of Activated Alkenes Using a Living Microorganism

Microorganisms can be programmed to perform chemical synthesis via metabolic engineering. However, despite an increasing interest in the use of de novo metabolic pathways and designer whole‐cells for small molecule synthesis, the inherent synthetic capabilities of native microorganisms remain underexplored. Herein, we report the use of unmodified E. coli BL21(DE3) cells for the reduction of keto‐acrylic compounds and apply this whole‐cell biotransformation to the synthesis of aminolevulinic acid from a lignin‐derived feedstock. The reduction reaction is rapid, chemo‐, and enantioselective, occurs under mild conditions (37 °C, aqueous media), and requires no toxic transition metals or external reductants. This study demonstrates the remarkable promiscuity of central metabolism in bacterial cells and how these processes can be leveraged for synthetic chemistry without the need for genetic manipulation.     

The Fundamentals of Real‐Time Surface Plasmon Resonance/Electrogenerated Chemiluminescence

We report the integration of surface plasmon resonance (SPR), cyclic voltammetry and electrochemiluminescence (ECL) responses to survey the interfacial adsorption and energy transfer processes involved in ECL on a plasmonic substrate. It was observed that a Tween 80/tripropylamine nonionic layer formed on the gold electrode of the SPR sensor, while enhancing the ECL emission process, affects the electron transfer process to the luminophore, Ru(bpy)₃²⁺, which in turn has an impact on the plasmon resonance. Concomitantly, the surface plasmon modulated the ECL intensity, which decreased by about 40 %, due to an interaction between the excited state of Ru(bpy)₃²⁺ and the plasmon. This occurred only when the plasmon was excited, demonstrating that the optically excited surface plasmon leads to lower plasmon‐mediated luminescence and that the plasmon interacts with the excited state of Ru(bpy)₃²⁺ within a very thin layer.     

Problem-driven scenario generation: an analytical approach for stochastic programs with tail risk measure

Mathematical Programming - Scenario generation is the construction of a discrete random vector to represent parameters of uncertain values in a stochastic program. Most approaches to scenario...     

Electrochemical methods for analysing and controlling charge transfer at the electrode–tissue interface

There have been rapid advances in the development of new materials for use in electrode–tissue interfacing. The development of conducting polymers, conducting hydrogels, carbon nanotubes, graphene and other conducting materials has provided a rich landscape for controlling charge transfer at the electrode–tissue interface and hence to monitor and manipulate cell behaviour. These materials have been used in tissue-engineered constructs to direct and control cell proliferation, growth and differentiation. However, their translation to clinical devices has been less successful. In this review, the use of electroanalytical techniques to develop an understanding of charge transfer at the electrode–tissue interface is discussed. In particular, the impact of solution and electrode conditions on charge injection capacity is demonstrated. The importance of standardised testing methods and the correlation of electrochemical and electrophysiological performance show the limitations of empirical studies and help define key electrode properties for clinical devices. The development of a sound theoretical basis for charge transfer at this increasingly important interface is being advocated to improve clinical outcomes and device lifetime and reduce power usage.