536 research outputs found
Experimental evaluation of a solid oxide fuel cell system exposed to inclinations and accelerations by ship motions
Solid Oxide Fuel Cell (SOFC) systems have the potential to reduce emissions from seagoing vessels. However, it is unknown whether ship motions influence the system's operation. In this research, a 1.5 kW SOFC module is operated on an inclination platform that emulates ship motions, to evaluate the influence of static and dynamic inclinations on the system's safety, operation, and lifetime. The test campaign consists of a static inclination test, a dynamic test, a degradation test, and a high acceleration test. There were no interruptions in the power supply during the different tests, and no detectable gas leakages or safety hazards. Although the SOFC does not fail in any test condition, dynamic inclinations result in forced oscillations in the fuel regulation, which propagate through the system by different feedback loops in the control architecture, leading to significant deviations in the operational parameters of the system. Additionally, for motion periods from 16 to 26 s, reoccurring exceedance of the fuel utilisation results in a gradual reduction of the power supply. Several enhancements are recommended to improve the design of SOFCs and marine fuel cell regulations to ensure their safe operation on ships.</p
Oropouche Virus Infection And Pathogenesis Are Restricted By Mavs, Irf-3, Irf-7, And Type I Interferon Signaling Pathways In Nonmyeloid Cells
Conselho Nacional de Desenvolvimento CientÃfico e Tecnológico (CNPq)Oropouche virus (OROV) is a member of the Orthobunyavirus genus in the Bunyaviridae family and a prominent cause of insect-transmitted viral disease in Central and South America. Despite its clinical relevance, little is known about OROV pathogenesis. To define the host defense pathways that control OROV infection and disease, we evaluated OROV pathogenesis and immune responses in primary cells and mice that were deficient in the RIG-I-like receptor signaling pathway (MDA5, RIG-I, or MAVS), downstream regulatory transcription factors (IRF-3 or IRF-7), beta interferon (IFN-beta), or the receptor for type I IFN signaling (IFNAR). OROV replicated to higher levels in primary fibroblasts and dendritic cells lacking MAVS signaling, the transcription factors IRF-3 and IRF-7, or IFNAR than in wild-type (WT) cells. In mice, deletion of IFNAR, MAVS, or IRF-3 and IRF-7 resulted in uncontrolled OROV replication, hypercytokinemia, extensive liver damage, and death, whereas WT congenic animals failed to develop disease. Unexpectedly, mice with a selective deletion of IFNAR on myeloid cells (CD11c Cre(+) Ifnar(f/f) or LysM Cre(+) Ifnar(f/f)) did not sustain enhanced disease with OROV or a selective (flox/flox) deletion La Crosse virus, a closely related encephalitic orthobunyavirus. In bone marrow chimera studies, recipient irradiated Ifnar(-/-) mice reconstituted with WT hematopoietic cells sustained high levels of OROV replication and liver damage, whereas WT mice reconstituted with Ifnar(-/-) bone marrow were resistant to disease. Collectively, these results establish a dominant protective role for MAVS, IRF-3 and IRF-7, and IFNAR in restricting OROV infection and tissue injury and suggest that IFN signaling in nonmyeloid cells contributes to the host defense against orthobunyaviruses.89947204737National Institutes of Health [R01 AI104972, P30 DK52574]Conselho Nacional de Desenvolvimento CientÃfico e Tecnológico (CNPq)University Research Committee grantConselho Nacional de Desenvolvimento CientÃfico e Tecnológico (CNPq)CNPq [246513/2012-8
Interferon-regulatory Factor 5-dependent Signaling Restricts Orthobunyavirus Dissemination To The Central Nervous System
Interferon (IFN)-regulatory factor 5 (IRF-5) is a transcription factor that induces inflammatory responses after engagement and signaling by pattern recognition receptors. To define the role of IRF-5 during bunyavirus infection, we evaluated Oropouche virus (OROV) and La Crosse virus (LACV) pathogenesis and immune responses in primary cells and in mice with gene deletions in Irf3, Irf5, and Irf7 or in Irf5 alone. Deletion of Irf3, Irf5, and Irf7 together resulted in uncontrolled viral replication in the liver and spleen, hypercytokinemia, extensive liver injury, and an early-death phenotype. Remarkably, deletion of Irf5 alone resulted in meningoencephalitis and death on a more protracted timeline, 1 to 2 weeks after initial OROV or LACV infection. The clinical signs in OROV-infected Irf5(-/-) mice were associated with abundant viral antigen and terminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL)-positive cells in several regions of the brain. Circulating dendritic cell (DC) subsets in Irf5(-/-) mice had higher levels of OROV RNA in vivo yet produced lower levels of type I IFN than wild-type (WT) cells. This result was supported by data obtained in vitro, since a deficiency of IRF-5 resulted in enhanced OROV infection and diminished type I IFN production in bone marrow-derived DCs. Collectively, these results indicate a key role for IRF-5 in modulating the host antiviral response in peripheral organs that controls bunyavirus neuroinvasion in mice.90118920
Transverse Dynamics and Energy Tuning of Fast Electrons Generated in Sub-Relativistic Intensity Laser Pulse Interaction with Plasmas
The regimes of quasi-mono-energetic electron beam generation were
experimentally studied in the sub-relativistic intensity laser plasma
interaction. The observed electron acceleration regime is unfolded with
two-dimensional-particle-in-cell simulations of laser-wakefield generation in
the self-modulation regime.Comment: 10 pages, 5 figure
A High Luminosity e+e- Collider to study the Higgs Boson
A strong candidate for the Standard Model Scalar boson, H(126), has been
discovered by the Large Hadron Collider (LHC) experiments. In order to study
this fundamental particle with unprecedented precision, and to perform
precision tests of the closure of the Standard Model, we investigate the
possibilities offered by An e+e- storage ring collider. We use a design
inspired by the B-factories, taking into account the performance achieved at
LEP2, and imposing a synchrotron radiation power limit of 100 MW. At the most
relevant centre-of-mass energy of 240 GeV, near-constant luminosities of 10^34
cm^{-2}s^{-1} are possible in up to four collision points for a ring of 27km
circumference. The achievable luminosity increases with the bending radius, and
for 80km circumference, a luminosity of 5 10^34 cm^{-2}s^{-1} in four collision
points appears feasible. Beamstrahlung becomes relevant at these high
luminosities, leading to a design requirement of large momentum acceptance both
in the accelerating system and in the optics. The larger machine could reach
the top quark threshold, would yield luminosities per interaction point of
10^36 cm^{-2}s^{-1} at the Z pole (91 GeV) and 2 10^35 cm^{-2}s^{-1} at the W
pair production threshold (80 GeV per beam). The energy spread is reduced in
the larger ring with respect to what is was at LEP, giving confidence that beam
polarization for energy calibration purposes should be available up to the W
pair threshold. The capabilities in term of physics performance are outlined.Comment: Submitted to the European Strategy Preparatory Group 01-04-2013 new
version as re-submitted to PRSTA
All-sky upper limit for gravitational radiation from spinning neutron stars
We present results of the all-sky search for gravitational-wave signals from
spinning neutron stars in the data of the EXPLORER resonant bar detector. Our
data analysis technique was based on the maximum likelihood detection method.
We briefly describe the theoretical methods that we used in our search. The
main result of our analysis is an upper limit of for
the dimensionless amplitude of the continuous gravitational-wave signals coming
from any direction in the sky and in the narrow frequency band from 921.00 Hz
to 921.76 Hz.Comment: 12 pages, 4 figures, submitted to Proceedings of 7th Gravitational
Wave Data Analysis Workshop, December 17-19, 2002, Kyoto, Japa
IRF-5-dependent signaling restricts Orthobunyavirus dissemination to the central nervous system
ABSTRACT Interferon (IFN)-regulatory factor 5 (IRF-5) is a transcription factor that induces inflammatory responses after engagement and signaling by pattern recognition receptors. To define the role of IRF-5 during bunyavirus infection, we evaluated Oropouche virus (OROV) and La Crosse virus (LACV) pathogenesis and immune responses in primary cells and in mice with gene deletions in Irf3 , Irf5 , and Irf7 or in Irf5 alone. Deletion of Irf3 , Irf5 , and Irf7 together resulted in uncontrolled viral replication in the liver and spleen, hypercytokinemia, extensive liver injury, and an early-death phenotype. Remarkably, deletion of Irf5 alone resulted in meningoencephalitis and death on a more protracted timeline, 1 to 2 weeks after initial OROV or LACV infection. The clinical signs in OROV-infected Irf5 −/− mice were associated with abundant viral antigen and terminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL)-positive cells in several regions of the brain. Circulating dendritic cell (DC) subsets in Irf5 −/− mice had higher levels of OROV RNA in vivo yet produced lower levels of type I IFN than wild-type (WT) cells. This result was supported by data obtained in vitro , since a deficiency of IRF-5 resulted in enhanced OROV infection and diminished type I IFN production in bone marrow-derived DCs. Collectively, these results indicate a key role for IRF-5 in modulating the host antiviral response in peripheral organs that controls bunyavirus neuroinvasion in mice. IMPORTANCE Oropouche virus (OROV) and La Crosse virus (LACV) are orthobunyaviruses that are transmitted by insects and cause meningitis and encephalitis in subsets of individuals in the Americas. Recently, we demonstrated that components of the type I interferon (IFN) induction pathway, particularly the regulatory transcription factors IRF-3 and IRF-7, have key protective roles during OROV infection. However, the lethality in Irf3 −/− Irf7 −/− (DKO) mice infected with OROV was not as rapid or complete as observed in Ifnar −/− mice, indicating that other transcriptional factors associated with an IFN response contribute to antiviral immunity against OROV. Here, we evaluated bunyavirus replication, tissue tropism, and cytokine production in primary cells and mice lacking IRF-5. We demonstrate an important role for IRF-5 in preventing neuroinvasion and the ensuing encephalitis caused by OROV and LACV
Design, Manufacturing Status, First Results of the LHC Main Dipole Final Prototypes and Steps towards Series Manufacture
This paper reports about the program of six LHC superconducting main dipole final prototypes and the steps towards series manufacture. The above program, launched in summer 1998, relies on collared coils manufactured by industry and cold masses assembled at the CERN Magnet Assembly Facility. Following design, stability and robustness studies, the magnet design for series manufacture features a "6-block" coil and austenitic steel collars. A general description of the magnet with its main components is given and the main working parameters and the most important manufacturing features are presented. Results of mechanical and magnetic measurements are given as well as the performances of the first prototype. A comparison with results from the previous generation of dipole magnet models and prototypes is also made. Finally an outlook towards series manufacture is given
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