550 research outputs found
Effects of Hyperbolic Rotation in Minkowski Space on the Modeling of Plasma Accelerators in a Lorentz Boosted Frame
Laser driven plasma accelerators promise much shorter particle accelerators
but their development requires detailed simulations that challenge or exceed
current capabilities. We report the first direct simulations of stages up to 1
TeV from simulations using a Lorentz boosted calculation frame resulting in a
million times speedup, thanks to a frame boost as high as gamma=1300. Effects
of the hyperbolic rotation in Minkowski space resulting from the frame boost on
the laser propagation in the plasma is shown to be key in the mitigation of a
numerical instability that was limiting previous attempts
Presence of New Delhi metallo-ÎČ-lactamase gene (NDM-1) in a clinical isolate of Acinetobacter junii in Argentina
Here we report the presence of a clinically significant A. junii blaNDM-1 positive in a 38-year-old woman who was admitted to the emergency department with a fever and leg ulcers with signs of infection. The NDM-1 carbapenemase has been dramatically spread among Gram-negative bacilli, thus imposing a new challenge on the health system to fight bacterial infections.These data expand the number of Acinetobacter species harbouring blaNDM-1. The wide existence of Acinetobacter harbouring and dispersing this carbapenemase emphasizes the importance of non-previously recognized pathogens as reservoirs of dangerous resistance determinants. These resistance determinants can be later easily transferred to other menacing pathogens.Fil: Montaña, Sabrina Daiana. Consejo Nacional de Investigaciones CientĂficas y TĂ©cnicas. Oficina de CoordinaciĂłn Administrativa Houssay. Instituto de Investigaciones en MicrobiologĂa y ParasitologĂa MĂ©dica. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones en MicrobiologĂa y ParasitologĂa MĂ©dica; ArgentinaFil: Cittadini, Roxana. Sanatorio Mater Dei; ArgentinaFil: Del Castillo M,. Sanatorio Mater Dei; ArgentinaFil: Uong, S.. California State University; Estados UnidosFil: Lazzaro, T.. California State University; Estados UnidosFil: Almuzara, Marisa. Consejo Nacional de Investigaciones CientĂficas y TĂ©cnicas; Argentina. Universidad de Buenos Aires. Facultad de Farmacia y BioquĂmica. Departamento de BioquĂmica ClĂnica; Argentina. Universidad de Buenos Aires. Facultad de Medicina. Hospital de ClĂnicas General San MartĂn; ArgentinaFil: Barberis, Claudia. Sanatorio Mater Dei; Argentina. Universidad de Buenos Aires. Facultad de Farmacia y BioquĂmica. Departamento de BioquĂmica ClĂnica; Argentina. Universidad de Buenos Aires. Facultad de Medicina. Hospital de ClĂnicas General San MartĂn; ArgentinaFil: Vay, Carlos Alberto. Consejo Nacional de Investigaciones CientĂficas y TĂ©cnicas; Argentina. Universidad de Buenos Aires. Facultad de Farmacia y BioquĂmica. Departamento de BioquĂmica ClĂnica; Argentina. Universidad de Buenos Aires. Facultad de Medicina. Hospital de ClĂnicas General San MartĂn; ArgentinaFil: RamĂrez, M. S.. California State University; Estados Unido
Quasi-monoenergetic femtosecond photon sources from Thomson Scattering using laser plasma accelerators and plasma channels
Narrow bandwidth, high energy photon sources can be generated by Thomson
scattering of laser light from energetic electrons, and detailed control of the
interaction is needed to produce high quality sources. We present analytic
calculations of the energy-angular spectra and photon yield that parametrize
the influences of the electron and laser beam parameters to allow source
design. These calculations, combined with numerical simulations, are applied to
evaluate sources using conventional scattering in vacuum and methods for
improving the source via laser waveguides or plasma channels. We show that the
photon flux can be greatly increased by using a plasma channel to guide the
laser during the interaction. Conversely, we show that to produce a given
number of photons, the required laser energy can be reduced by an order of
magnitude through the use of a plasma channel. In addition, we show that a
plasma can be used as a compact beam dump, in which the electron beam is
decelerated in a short distance, thereby greatly reducing radiation shielding.
Realistic experimental errors such as transverse jitter are quantitatively
shown to be tolerable. Examples of designs for sources capable of performing
nuclear resonance fluorescence and photofission are provided
Rapid convective outflow from the U.S. to the upper troposphere over the North Atlantic during the NASA INTEX-NA airborne campaign: flight 13 case study
International audienceA case study of convective outflow from the United States (U.S.) was examined using airborne measurements from NASA DC-8 flight 13 during the Intercontinental Chemical Transport Experiment ? North America (INTEX-NA). Mixing ratios of methane (CH4) and carbon monoxide (CO) at 8?11 km altitude over the North Atlantic were elevated to 1843 ppbv and 134 ppbv respectively, while those of carbon dioxide (CO2) and carbonyl sulfide (COS) were reduced to 372.4 ppmv and 411 pptv respectively. In this region, urban and industrial influence was evidenced by elevated mixing ratios and good linear relationships between urban and industrial tracers compared to North Atlantic background air. Moreover, low mixing ratios and a good correlation between COS and CO2 showed a fingerprint of terrestrial uptake and minimal dilution during rapid transport over a 1?2 day time period. Analysis of synoptic conditions, backward trajectories, and photochemical aging estimates based on C3H8/C2H6 strongly suggested that elevated anthropogenic tracers in the upper troposphere of the flight region were the result of fast transport via convective uplifting of boundary layer air over the southeastern U.S. This mechanism is supported by the similar slopes values of linear correlations between long-lived (months) anthropogenic tracers (e.g., C2Cl4 and CHCl3) from the flight region and the planetary boundary layer in the southeastern U.S. In addition, the aircraft measurements suggest that outflow from the U.S. augmented the entire tropospheric column at mid-latitudes over the North Atlantic. Overall, the flight 13 data demonstrate a pervasive impact of U.S. anthropogenic emissions on the troposphere over the North Atlantic
Continental outflow from the US to the upper troposphere over the North Atlantic during the NASA INTEX-NA Airborne Campaign
A case of continental outflow from the United States (US) was examined using airborne measurements from NASA DC-8 flight 13 during the Intercontinental Chemical Transport Experiment &ndash; North America (INTEX-NA). Mixing ratios of methane (CH<sub>4</sub>) and carbon monoxide (CO) at 8&ndash;11 km altitude over the North Atlantic were elevated to 1843 ppbv and 134 ppbv respectively, while those of carbon dioxide (CO<sub>2</sub>) and carbonyl sulfide (COS) were reduced to 372.4 ppmv and 411 pptv respectively. In this region, urban and industrial influences were evidenced by elevated mixing ratios and good linear relationships between urban and industrial tracers compared to North Atlantic background air. Moreover, low mixing ratios and a good correlation between COS and CO<sub>2</sub> showed a fingerprint of terrestrial uptake and minimal dilution during rapid transport over a 1&ndash;2 day time period. Analysis of synoptic conditions, backward trajectories, and photochemical aging estimates based on C<sub>3</sub>H<sub>8</sub>/C<sub>2</sub>H<sub>6</sub> strongly suggested that elevated anthropogenic tracers in the upper troposphere of the flight region were the result of transport via convection and warm conveyor belt (WCB) uplifting of boundary layer air over the southeastern US. This mechanism is supported by the similar slope values of linear correlations between long-lived (months) anthropogenic tracers (e.g., C<sub>2</sub>Cl<sub>4</sub> and CHCl<sub>3</sub>) from the flight region and the planetary boundary layer in the southeastern US. In addition, the aircraft measurements suggest that outflow from the US augmented the entire tropospheric column at mid-latitudes over the North Atlantic. Overall, the flight 13 data demonstrate a pervasive impact of US anthropogenic emissions on the troposphere over the North Atlantic
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Ozone production in the upper troposphere and the influence of aircraft during SONEX: Approach of NO(x)-saturated conditions
During October/November 1997, simultaneous observations of NO, HO2 and other species were obtained as part of the SONEX campaign in the upper troposphere. We use these observations, over the North Atlantic (40-60°N), to derive ozone production rates, P(O3), and to examine the relationship between P(O3) and the concentrations of NO(x) (= NO + NO2) and HO(x) (= OH + peroxy) radicals. A positive correlation is found between P(O3) and NO(x) over the entire data set, which reflects the association of elevated HO(x) with elevated NO(x) injected by deep convection and lightning. By filtering out this association we find that for NO(x)>70 pptv, P(O3) is nearly independent of NO(x), showing the approach of NO(x)-saturated conditions. Predicted doubling of aircraft emissions in the future will result in less than doubling of the aircraft contribution to ozone over the North Atlantic in the fall. Greater sensitivity to aircraft emissions would be expected in the summer
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Contribution of biomass and biofuel emissions to trace gas distributions in Asia during the TRACE-P experiment
Low transverse emittance electron bunches from two-color laser-ionization injection
A method is proposed to generate low emittance electron bunches from two
color laser pulses in a laser-plasma accelerator. A two-region gas structure is
used, containing a short region of a high-Z gas (e.g., krypton) for ionization
injection, followed by a longer region of a low-Z gas for post-acceleration. A
long-laser-wavelength (e.g., 5 micron) pump pulse excites plasma wake without
triggering the inner-shell electron ionization of the high-Z gas due to low
electric fields. A short-laser-wavelength (e.g., 0.4 micron) injection pulse,
located at a trapping phase of the wake, ionizes the inner-shell electrons of
the high-Z gas, resulting in ionization-induced trapping. Compared with a
single-pulse ionization injection, this scheme offers an order of magnitude
smaller residual transverse momentum of the electron bunch, which is a result
of the smaller vector potential amplitude of the injection pulse
In situ measurements of tropospheric volcanic plumes in Ecuador and Colombia during TC^4
A NASA DC-8 research aircraft penetrated tropospheric gas and aerosol plumes sourced from active volcanoes in Ecuador and Colombia during the Tropical Composition, Cloud and Climate Coupling (TC^4) mission in JulyâAugust 2007. The likely source volcanoes were Tungurahua (Ecuador) and Nevado del Huila (Colombia). The TC^4 data provide rare insight into the chemistry of volcanic plumes in the tropical troposphere and permit a comparison of SO_2 column amounts measured by the Ozone Monitoring Instrument (OMI) on the Aura satellite with in situ SO_2 measurements. Elevated concentrations of SO_2, sulfate aerosol, and particles were measured by DC-8 instrumentation in volcanic outflow at altitudes of 3â6 km. Estimated plume ages range from ~2 h at Huila to ~22â48 h downwind of Ecuador. The plumes contained sulfate-rich accumulation mode particles that were variably neutralized and often highly acidic. A significant fraction of supermicron volcanic ash was evident in one plume. In-plume O_3 concentrations were ~70%â80% of ambient levels downwind of Ecuador, but data are insufficient to ascribe this to O_3 depletion via reactive halogen chemistry. The TC^4 data record rapid cloud processing of the Huila volcanic plume involving aqueous-phase oxidation of SO_2 by H_2O_2, but overall the data suggest average in-plume SO_2 to sulfate conversion rates of ~1%â2% h^(â1). SO_2 column amounts measured in the Tungurahua plume (~0.1â0.2 Dobson units) are commensurate with average SO_2 columns retrieved from OMI measurements in the volcanic outflow region in July 2007. The TC^4 data set provides further evidence of the impact of volcanic emissions on tropospheric acidity and oxidizing capacity
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