38 research outputs found
The Physics of Cluster Mergers
Clusters of galaxies generally form by the gravitational merger of smaller
clusters and groups. Major cluster mergers are the most energetic events in the
Universe since the Big Bang. Some of the basic physical properties of mergers
will be discussed, with an emphasis on simple analytic arguments rather than
numerical simulations. Semi-analytic estimates of merger rates are reviewed,
and a simple treatment of the kinematics of binary mergers is given. Mergers
drive shocks into the intracluster medium, and these shocks heat the gas and
should also accelerate nonthermal relativistic particles. X-ray observations of
shocks can be used to determine the geometry and kinematics of the merger. Many
clusters contain cooling flow cores; the hydrodynamical interactions of these
cores with the hotter, less dense gas during mergers are discussed. As a result
of particle acceleration in shocks, clusters of galaxies should contain very
large populations of relativistic electrons and ions. Electrons with Lorentz
factors gamma~300 (energies E = gamma m_e c^2 ~ 150 MeV) are expected to be
particularly common. Observations and models for the radio, extreme
ultraviolet, hard X-ray, and gamma-ray emission from nonthermal particles
accelerated in these mergers are described.Comment: 38 pages with 9 embedded Postscript figures. To appear in Merging
Processes in Clusters of Galaxies, edited by L. Feretti, I. M. Gioia, and G.
Giovannini (Dordrecht: Kluwer), in press (2001
Atomistic characterization of the active-site solvation dynamics of a model photocatalyst
The interactions between the reactive excited state of molecular photocatalysts and surrounding solvent dictate reaction mechanisms and pathways, but are not readily accessible to conventional optical spectroscopic techniques. Here we report an investigation of the structural and solvation dynamics following excitation of a model photocatalytic molecular system [Ir 2 (dimen) 4 ] 2+, where dimen is para-diisocyanomenthane. The time-dependent structural changes in this model photocatalyst, as well as the changes in the solvation shell structure, have been measured with ultrafast diffuse X-ray scattering and simulated with Born-Oppenheimer Molecular Dynamics. Both methods provide direct access to the solute-solvent pair distribution function, enabling the solvation dynamics around the catalytically active iridium sites to be robustly characterized. Our results provide evidence for the coordination of the iridium atoms by the acetonitrile solvent and demonstrate the viability of using diffuse X-ray scattering at free-electron laser sources for studying the dynamics of photocatalysis. © The Author(s) 201617111sciescopu
No association between intake of marine n-3 polyunsaturated fatty acids during second trimester of pregnancy and factors associated with cardiometabolic risk in the 20 year old off-spring
Supplementary Material for: Biomarker Discovery by Mass Spectrometry in Cerebrospinal Fluid and Plasma after Global Hypoxia-Ischemia in Newborn Piglets
<b><i>Background:</i></b> Biomarkers may qualify diagnosis, treatment allocation, and prognostication in neonatal encephalopathy. Biomarker development is challenged by competing etiologies, inter-individual genetic variability, and a lack of specific neonatal markers. To address these challenges, we used a standardized neonatal hypoxic-ischemic (HI) encephalopathy model with pre- and post-HI sampling of cerebrospinal fluid (CSF) and plasma. <b><i>Objectives:</i></b> The study aimed to identify novel candidate protein biomarkers of HI encephalopathy in a newborn piglet model in CSF and plasma. <b><i>Methods:</i></b> F<sub>i</sub>O<sub>2</sub> was lowered to 4% in 6 newborn piglets, then adjusted over a 45-min period keeping the amplitude integrated-EEG < 7 µV to induce HI encephalopathy. CSF and plasma was sampled pre-HI and 2 h after HI, protein levels were then analyzed by mass spectrometry. <b><i>Results:</i></b> Protein levels after HI changed significantly for 18 CSF proteins and 37 plasma proteins. CSF and plasma data showed distinct information, although peptidyl-prolyl cis-trans isomerase A had elevated levels in both fluids. HI regulation involved functional groups such as the antioxidant system, cell proliferation, cell structure, and apoptosis. S100-A8, which increased the most in CSF (9.5 fold), is known to be involved in inflammatory and immune response and to be highly regulated during injury. In plasma, increased proteins included FABP1 (31.8 fold) and proteins with antioxidant (SOD1, GPX3) and lectin function (REG3A, LGALS3). <b><i>Conclusions:</i></b> In this exploratory study, we have identified candidate biomarkers for HI in CSF and plasma, many not previously associated with HI. Identified proteins are promising candidates for further validation in time series experiments and clinical studies