Verification of CPT-invariance of QED bound states for the production of muonium or antimuonium in scattering of electrons or positrons by nuclei

A possibility of a verification of CPT-invariance of QED for bound states by example of muonium or antimuonium produced in reactions of scattering of electrons or positrons by nuclei is considered. The number of events of the muonium production is estimated for contemporary accelerators. The method of the detection of muonium by measuring of oscillations of the decay curve caused by the interference between the ground and excited state of muonium is suggested. The admixture of the excited muonium to the final state is calculated.Comment: 7 pages, 3 figures, Latex, published in JETP 74, 196 (2001), corrected mistypes in eqs. (2.2), (2.4), (2.7

Post‐discharge tobacco cessation rates among hospitalized US veterans with and without diabetes

Aims  Smoking is a major risk factor for cardiovascular complications among patients with diabetes. Hospitalization has been shown to enhance cessation rates. The purpose of this study was to compare 6‐month post‐hospitalization tobacco cessation rates among US veterans with and without diabetes. Methods  This was a longitudinal study among inpatient veterans who used tobacco in the past month ( n  = 496). Patients were recruited and surveyed from three Midwestern Department of Veterans Affairs hospitals during an acute‐care hospitalization. They were also asked to complete a follow‐up survey 6 months post‐discharge. Bivariate‐ and multivariable‐adjusted analyses were conducted to determine differences in tobacco cessation rates between patients with and without a diagnosis of diabetes. Results  The mean age of patients was 55.2 years and 62% were white. Twenty‐nine per cent had co‐morbid diabetes. A total of 18.8% of patients with diabetes reported tobacco cessation at 6 months compared with 10.9% of those without diabetes ( P  = 0.02). Cotinine‐verified cessation rates were 12.5 vs. 7.4% in the groups with and without diabetes, respectively ( P  = 0.07). Controlling for psychiatric co‐morbidities, depressive symptoms, age, self‐rated health and nicotine dependence, the multivariable‐adjusted logistic regression showed that patients with diabetes had three times higher odds of 6‐month cotinine‐verified tobacco cessation as compared with those without diabetes (odds ratio 3.17, P  = 0.005). Conclusions  Post‐hospitalization rates of smoking cessation are high among those with diabetes. Intensive tobacco cessation programmes may increase these cessation rates further.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/92145/1/j.1464-5491.2012.03635.x.pd

Synthetic ozone deposition and stomatal uptake at flux tower sites

We develop and evaluate a method to estimate O-3 deposition and stomatal O-3 uptake across networks of eddy covariance flux tower sites where O-3 concentrations and O-3 fluxes have not been measured. The method combines standard micrometeorological flux measurements, which constrain O-3 deposition velocity and stomatal conductance, with a gridded dataset of observed surface O-3 concentrations. Measurement errors are propagated through all calculations to quantify O-3 flux uncertainties. We evaluate the method at three sites with O(3 )flux measurements: Harvard Forest, Blodgett Forest, and Hyytiala Forest. The method reproduces 83 % or more of the variability in daily stomatal uptake at these sites with modest mean bias (21 % or less). At least 95 % of daily average values agree with measurements within a factor of 2 and, according to the error analysis, the residual differences from measured O-3 fluxes are consistent with the uncertainty in the underlying measurements. The product, called synthetic O-3 flux or SynFlux, includes 43 FLUXNET sites in the United States and 60 sites in Europe, totaling 926 site years of data. This dataset, which is now public, dramatically expands the number and types of sites where O-3 fluxes can be used for ecosystem impact studies and evaluation of air quality and climate models. Across these sites, the mean stomatal conductance and O-3 deposition velocity is 0.03-1.0 cm s(-1). The stomatal O-3 flux during the growing season (typically April-September) is 0.5-11.0 nmol O-3 m(-2) s(-1) with a mean of 4.5 nmol O(3 )m(-2) s(-1) and the largest fluxes generally occur where stomatal conductance is high, rather than where O-3 concentrations are high. The conductance differences across sites can be explained by atmospheric humidity, soil moisture, vegetation type, irrigation, and land management. These stomatal fluxes suggest that ambient O-3 degrades biomass production and CO2 sequestration by 20 %-24 % at crop sites, 6 %-29 % at deciduous broadleaf forests, and 4 %-20 % at evergreen needleleaf forests in the United States and Europe.Peer reviewe

Canopy nitrogen, carbon assimilation, and albedo in temperate and boreal forests: Functional relations and potential climate feedbacks

The availability of nitrogen represents a key constraint on carbon cycling in terrestrial ecosystems, and it is largely in this capacity that the role of N in the Earth\u27s climate system has been considered. Despite this, few studies have included continuous variation in plant N status as a driver of broad-scale carbon cycle analyses. This is partly because of uncertainties in how leaf-level physiological relationships scale to whole ecosystems and because methods for regional to continental detection of plant N concentrations have yet to be developed. Here, we show that ecosystem CO2 uptake capacity in temperate and boreal forests scales directly with whole-canopy N concentrations, mirroring a leaf-level trend that has been observed for woody plants worldwide. We further show that both CO2 uptake capacity and canopy N concentration are strongly and positively correlated with shortwave surface albedo. These results suggest that N plays an additional, and overlooked, role in the climate system via its influence on vegetation reflectivity and shortwave surface energy exchange. We also demonstrate that much of the spatial variation in canopy N can be detected by using broad-band satellite sensors, offering a means through which these findings can be applied toward improved application of coupled carbon cycle–climate models

Chemo- and Thermosensory Responsiveness of Grueneberg Ganglion Neurons Relies on Cyclic Guanosine Monophosphate Signaling Elements

Neurons of the Grueneberg ganglion (GG) in the anterior nasal region of mouse pups respond to cool temperatures and to a small set of odorants. While the thermosensory reactivity appears to be mediated by elements of a cyclic guanosine monophosphate (cGMP) cascade, the molecular mechanisms underlying the odor-induced responses are unclear. Since odor-responsive GG cells are endowed with elements of a cGMP pathway, specifically the transmembrane guanylyl cyclase subtype GC-G and the cyclic nucleotide-gated ion channel CNGA3, the possibility was explored whether these cGMP signaling elements may also be involved in chemosensory GG responses. Experiments with transgenic mice deficient for GC-G or CNGA3 revealed that GG responsiveness to given odorants was significantly diminished in these knockout animals. These findings suggest that a cGMP cascade may be important for both olfactory and thermosensory signaling in the GG. However, in contrast to the thermosensory reactivity, which did not decline over time, the chemosensory response underwent adaptation upon extended stimulation, suggesting that the two transduction processes only partially overlap. Copyright (C) 2011 S. Karger AG, Base

Atomic Alchemy

We consider the transitions between electromagnetic bound states, such as the exclusive weak decay of a muonic atom into an electronic atom: $(\mu^- Z) \to (e^- Z) {\bar \nu_e }\nu_\mu .$ We show that relativistic effects in the atomic wavefunctions are crucial for determining the rate. In the case of heavy atoms, the exclusive channel branching ratios exceed $10^{-6},$ possibly bringing the study of these rare decays within experimental reach. Such processes thus provide a detailed laboratory for studying the high momentum tail of wavefunctions in atomic physics; in addition, they provide a simple toy model for investigating analogous exclusive heavy hadronic decays in quantum chromodynamics such as $B \to \pi e \nu.$Comment: 16 pages and 5 Figures, SLAC-PUB-648

Regulation of protein abundance in genetically diverse mouse populations.

Genetically diverse mouse populations are powerful tools for characterizing the regulation of the proteome and its relationship to whole-organism phenotypes. We used mass spectrometry to profile and quantify the abundance of 6,798 proteins in liver tissue from mice of both sexes across 58 Collaborative Cross (CC) inbred strains. We previously collected liver proteomics data from the related Diversity Outbred (DO) mice and their founder strains. We show concordance across the proteomics datasets despite being generated from separate experiments, allowing comparative analysis. We map protein abundance quantitative trait loci (pQTLs), identifying 1,087 local and 285 distal in the CC mice and 1,706 local and 414 distal in the DO mice. We find that regulatory effects on individual proteins are conserved across the mouse populations, in particular for local genetic variation and sex differences. In comparison, proteins that form complexes are often co-regulated, displaying varying genetic architectures, and overall show lower heritability and map fewer pQTLs. We have made this resource publicly available to enable quantitative analyses of the regulation of the proteome

Genetic dissection of the pluripotent proteome through multi-omics data integration.

Genetic background drives phenotypic variability in pluripotent stem cells (PSCs). Most studies to date have used transcript abundance as the primary molecular readout of cell state in PSCs. We performed a comprehensive proteogenomics analysis of 190 genetically diverse mouse embryonic stem cell (mESC) lines. The quantitative proteome is highly variable across lines, and we identified pluripotency-associated pathways that were differentially activated in the proteomics data that were not evident in transcriptome data from the same lines. Integration of protein abundance to transcript levels and chromatin accessibility revealed broad co-variation across molecular layers as well as shared and unique drivers of quantitative variation in pluripotency-associated pathways. Quantitative trait locus (QTL) mapping localized the drivers of these multi-omic signatures to genomic hotspots. This study reveals post-transcriptional mechanisms and genetic interactions that underlie quantitative variability in the pluripotent proteome and provides a regulatory map for mESCs that can provide a basis for future mechanistic studies