The effect of deuteration on organic magnetoresistance

NOTICE: this is the author’s version of a work that was accepted for publication in Synthetic Metals. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in SYNTHETIC METALS, 161, 7-8, (2011) DOI 10.1016/j.synthmet.2010.11.04

The "physical process" version of the first law and the generalized second law for charged and rotating black holes

We investigate both the ``physical process'' version of the first law and the second law of black hole thermodynamics for charged and rotating black holes. We begin by deriving general formulas for the first order variation in ADM mass and angular momentum for linear perturbations off a stationary, electrovac background in terms of the perturbed non-electromagnetic stress-energy, $\delta T_{ab}$, and the perturbed charge current density, $\delta j^a$. Using these formulas, we prove the "physical process version" of the first law for charged, stationary black holes. We then investigate the generalized second law of thermodynamics (GSL) for charged, stationary black holes for processes in which a box containing charged matter is lowered toward the black hole and then released (at which point the box and its contents fall into the black hole and/or thermalize with the ``thermal atmosphere'' surrounding the black hole). Assuming that the thermal atmosphere admits a local, thermodynamic description with respect to observers following orbits of the horizon Killing field, and assuming that the combined black hole/thermal atmosphere system is in a state of maximum entropy at fixed mass, angular momentum, and charge, we show that the total generalized entropy cannot decrease during the lowering process or in the ``release process''. Consequently, the GSL always holds in such processes. No entropy bounds on matter are assumed to hold in any of our arguments.Comment: 35 pages; 1 eps figur

Project Coolbit: Can your watch predict heat stress and thermal comfort sensation?

10.1088/1748-9326/abd130ENVIRONMENTAL RESEARCH LETTERS16

Chronic Ketamine Administration Modulates Midbrain Dopamine System in Mice

Ketamine is an anesthetic and a popular abusive drug. As an anesthetic, effects of ketamine on glutamate and GABA transmission have been well documented but little is known about its long-term effects on the dopamine system. In the present study, the effects of ketamine on dopamine were studied in vitro and in vivo. In pheochromocytoma (PC 12) cells and NGF differentiated-PC 12 cells, ketamine decreased the cell viability while increasing dopamine (DA) concentrations in a dose-related manner. However, ketamine did not affect the expression of genes involved in DA synthesis. In the long-term (3 months) ketamine treated mice, significant increases of DA contents were found in the midbrain. Increased DA concentrations were further supported by up-regulation of tyrosine hydroxylase (TH), the rate limiting enzyme in catecholamine synthesis. Activation of midbrain dopaminergic neurons could be related to ketamine modulated cortical-subcortical glutamate connections. Using western blotting, significant increases in BDNF protein levels were found in the midbrain, suggesting that perhaps BDNF pathways in the cortical-subcortical connections might contribute to the long-term ketamine induced TH upregulation. These data suggest that long-term ketamine abuse caused a delayed and persistent upregulation of subcortical DA systems, which may contribute to the altered mental status in ketamine abusers

Hot-mode accretion and the physics of thin-disc galaxy formation

We use FIRE simulations to study disc formation in z ∼ 0, Milky Way-mass galaxies, and conclude that a key ingredient for the formation of thin stellar discs is the ability for accreting gas to develop an aligned angular momentum distribution via internal cancellation prior to joining the galaxy. Among galaxies with a high fraction (⁠>70 per cent⁠) of their young stars in a thin disc (h/R ∼ 0.1), we find that: (i) hot, virial-temperature gas dominates the inflowing gas mass on halo scales (≳20 kpc), with radiative losses offset by compression heating; (ii) this hot accretion proceeds until angular momentum support slows inward motion, at which point the gas cools to ≲104K⁠; (iii) prior to cooling, the accreting gas develops an angular momentum distribution that is aligned with the galaxy disc, and while cooling transitions from a quasi-spherical spatial configuration to a more-flattened, disc-like configuration. We show that the existence of this ‘rotating cooling flow’ accretion mode is strongly correlated with the fraction of stars forming in a thin disc, using a sample of 17 z ∼ 0 galaxies spanning a halo mass range of 1010.5 M⊙ ≲ Mh ≲ 1012 M⊙ and stellar mass range of 108 M⊙ ≲ M⋆ ≲ 1011 M⊙. Notably, galaxies with a thick disc or irregular morphology do not undergo significant angular momentum alignment of gas prior to accretion and show no correspondence between halo gas cooling and flattening. Our results suggest that rotating cooling flows (or, more generally, rotating subsonic flows) that become coherent and angular momentum-supported prior to accretion on to the galaxy are likely a necessary condition for the formation of thin, star-forming disc galaxies in a ΛCDM universe

CCL3L1 Copy Number Variation and Susceptibility to HIV-1 Infection: A Meta-Analysis

Background: Although several studies have investigated whether CCL3L1 copy number variation (CNV) influences the risk of HIV-1 infection, there are still no clear conclusions. Therefore, we performed a meta-analysis using two models to generate a more robust estimate of the association between CCL3L1 CNV and susceptibility to HIV-1 infection. Methods: We divided the cases and controls into two parts as individuals with CCL3L1 gene copy number (GCN) above the population specific median copy number (PMN) and individuals with CCL3L1 GCN below PMN, respectively. Odds ratios (ORs) with 95 % confidence intervals (95 % CIs) were given for the main analysis. We also conducted stratified analyses by ethnicity, age group and sample size. Relevant literatures were searched through PubMed and ISI Web of Knowledge up t

Motion microscopy for visualizing and quantifying small motions

Although the human visual system is remarkable at perceiving and interpreting motions, it has limited sensitivity, and we cannot see motions that are smaller than some threshold. Although difficult to visualize, tiny motions below this threshold are important and can reveal physical mechanisms, or be precursors to large motions in the case of mechanical failure. Here, we present a “motion microscope,” a computational tool that quantifies tiny motions in videos and then visualizes them by producing a new video in which the motions are made large enough to see. Three scientific visualizations are shown, spanning macroscopic to nanoscopic length scales. They are the resonant vibrations of a bridge demonstrating simultaneous spatial and temporal modal analysis, micrometer vibrations of a metamaterial demonstrating wave propagation through an elastic matrix with embedded resonating units, and nanometer motions of an extracellular tissue found in the inner ear demonstrating a mechanism of frequency separation in hearing. In these instances, the motion microscope uncovers hidden dynamics over a variety of length scales, leading to the discovery of previously unknown phenomena

Gene Expression Changes in GABAA Receptors and Cognition Following Chronic Ketamine Administration in Mice

Ketamine is a well-known anesthetic agent and a drug of abuse. Despite its widespread use and abuse, little is known about its long-term effects on the central nervous system. The present study was designed to evaluate the effect of long-term (1- and 3-month) ketamine administration on learning and memory and associated gene expression levels in the brain. The Morris water maze was used to assess spatial memory and gene expression changes were assayed using Affymetrix Genechips; a focus on the expression of GABAA receptors that mediate a tonic inhibition in the brain, was confirmed by quantitative real-time PCR and western blot. Compared with saline controls, there was a decline in learning and memory performance in the ketamine-treated mice. Genechip results showed that 110 genes were up-regulated and 136 genes were down-regulated. An ontology analysis revealed the most significant effects of ketamine were on GABAA receptors. In particular, there was a significant up-regulation of both mRNA and protein levels of the alpha 5 subunit (Gabra5) of the GABAA receptors in the prefrontal cortex. In conclusion, chronic exposure to ketamine impairs working memory in mice, which may be explained at least partly by up-regulation of Gabra5 subunits in the prefrontal cortex