44 research outputs found
Recoil Polarization for Delta Excitation in Pion Electroproduction
We measured angular distributions of recoil-polarization response functions
for neutral pion electroproduction for W=1.23 GeV at Q^2=1.0 (GeV/c)^2,
obtaining 14 separated response functions plus 2 Rosenbluth combinations; of
these, 12 have been observed for the first time. Dynamical models do not
describe quantities governed by imaginary parts of interference products well,
indicating the need for adjusting magnitudes and phases for nonresonant
amplitudes. We performed a nearly model-independent multipole analysis and
obtained values for Re(S1+/M1+)=-(6.84+/-0.15)% and Re(E1+/M1+)=-(2.91+/-0.19)%
that are distinctly different from those from the traditional Legendre analysis
based upon M1+ dominance and sp truncation.Comment: 5 pages, 2 figures, for PR
Virtual Compton Scattering and Neutral Pion Electroproduction in the Resonance Region up to the Deep Inelastic Region at Backward Angles
We have made the first measurements of the virtual Compton scattering (VCS)
process via the H exclusive reaction in the nucleon resonance
region, at backward angles. Results are presented for the -dependence at
fixed GeV, and for the -dependence at fixed near 1.5 GeV.
The VCS data show resonant structures in the first and second resonance
regions. The observed -dependence is smooth. The measured ratio of
H to H cross sections emphasizes the different
sensitivity of these two reactions to the various nucleon resonances. Finally,
when compared to Real Compton Scattering (RCS) at high energy and large angles,
our VCS data at the highest (1.8-1.9 GeV) show a striking -
independence, which may suggest a transition to a perturbative scattering
mechanism at the quark level.Comment: 20 pages, 8 figures. To appear in Phys.Rev.
Predominance of null mutations in ataxia-telangiectasia
Ataxia-telangiectasia (A-T) is an autosomal recessive disorder involving cerebellar degeneration, immunodeficiency, chromosomal instability, radiosensitivity and cancer predisposition. The responsible gene, ATM, was recently identified by positional cloning and found to encode a putative 350 kDa protein with a PI 3-kinase-like domain, presumably involved in mediating cell cycle arrest in response to radiation-induced DNA damage. The nature and location of A-T mutations should provide insight into the function of the ATM protein and the molecular basis of this pleiotropic disease. Of 44 A-T mutations identified by us to date, 39 (89%) are expected to inactivate the ATM protein by truncating it, by abolishing correct initiation or termination of translation, or by deleting large segments. Additional mutations are four smaller in-frame deletions and insertions, and one substitution of a highly conserved amino acid at the PI 3-kinase domain. The emerging profile of mutations causing A-T is thus dominated by those expected to completely inactivate the ATM protein. ATM mutations with milder effects may result in phenotypes related, but not identical, to A-T
Dynamics of the O(e,e'p) cross section at high missing energies
We measured the cross section and response functions (R_L, R_T, and R_LT) for the 16O(e,e'p) reaction in quasielastic kinematics for missing energies 25 60 MeV and P_miss > 200 MeV/c, the cross section is relatively constant. Calculations which include contributions from pion exchange currents, isobar currents and short-range correlations account for the shape and the transversity but only for half of the magnitude of the measured cross section
High Precision Measurement of the Proton Elastic Form Factor Ratio at low
We report a new, high-precision measurement of the proton elastic form factor
ratio \mu_p G_E/G_M for the four-momentum transfer squared Q^2 = 0.3-0.7
(GeV/c)^2. The measurement was performed at Jefferson Lab (JLab) in Hall A
using recoil polarimetry. With a total uncertainty of approximately 1%, the new
data clearly show that the deviation of the ratio \mu_p G_E/G_M from unity
observed in previous polarization measurements at high Q^2 continues down to
the lowest Q^2 value of this measurement. The updated global fit that includes
the new results yields an electric (magnetic) form factor roughly 2% smaller
(1% larger) than the previous global fit in this Q^2 range. We obtain new
extractions of the proton electric and magnetic radii, which are
^(1/2)=0.875+/-0.010 fm and ^(1/2)=0.867+/-0.020 fm. The charge
radius is consistent with other recent extractions based on the electron-proton
interaction, including the atomic hydrogen Lamb shift measurements, which
suggests a missing correction in the comparison of measurements of the proton
charge radius using electron probes and the recent extraction from the muonic
hydrogen Lamb shift.Comment: 12 pages, 3 figure
Measurement of the single-spin asymmetry A y 0 in quasi-elastic 3He↑(e,e′n) scattering at 0.4 < Q 2 < 1.0 GeV/c 2
No abstract available
Global monitoring of antimicrobial resistance based on metagenomics analyses of urban sewage
Antimicrobial resistance (AMR) is a serious threat to global public health, but obtaining representative data on AMR for healthy human populations is difficult. Here, we use meta-genomic analysis of untreated sewage to characterize the bacterial resistome from 79 sites in 60 countries. We find systematic differences in abundance and diversity of AMR genes between Europe/North-America/Oceania and Africa/Asia/South-America. Antimicrobial use data and bacterial taxonomy only explains a minor part of the AMR variation that we observe. We find no evidence for cross-selection between antimicrobial classes, or for effect of air travel between sites. However, AMR gene abundance strongly correlates with socio-economic, health and environmental factors, which we use to predict AMR gene abundances in all countries in the world. Our findings suggest that global AMR gene diversity and abundance vary by region, and that improving sanitation and health could potentially limit the global burden of AMR. We propose metagenomic analysis of sewage as an ethically acceptable and economically feasible approach for continuous global surveillance and prediction of AMR.Peer reviewe
Setting a baseline for global urban virome surveillance in sewage
The rapid development of megacities, and their growing connectedness across the world is becoming a distinct driver for emerging disease outbreaks. Early detection of unusual disease emergence and spread should therefore include such cities as part of risk-based surveillance. A catch-all metagenomic sequencing approach of urban sewage could potentially provide an unbiased insight into the dynamics of viral pathogens circulating in a community irrespective of access to care, a potential which already has been proven for the surveillance of poliovirus. Here, we present a detailed characterization of sewage viromes from a snapshot of 81 high density urban areas across the globe, including in-depth assessment of potential biases, as a proof of concept for catch-all viral pathogen surveillance. We show the ability to detect a wide range of viruses and geographical and seasonal differences for specific viral groups. Our findings offer a cross-sectional baseline for further research in viral surveillance from urban sewage samples and place previous studies in a global perspective