421 research outputs found

    Relevance of d-D interactions on neutron and tritium production in IFMIF-EVEDA accelerator prototype

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    In the IFMIF-EVEDA accelerator prototype, deuterium is implanted in the components due to beam losses and in the beam dump, where the beam is stopped. The interaction of the deuterons with the deuterium previously implanted leads to the production of neutrons and tritium, which are important issues for radioprotection and safety analysis. A methodology to assess these production pathways in more realistic approach has been developed. The new tools and their main achievement are: (i) an “effective diffusivity coefficient” (deduced from available experimental data) that enables simulation of the diffusion phase, and (ii) the MCUNED code (able to handle deuteron transport libraries) allows to simulate the transport-slowdown of deuteron/tritium (to get the concentration profiles) and the neutron/tritium productions from d-Cu and d-D for up to 9 MeV incident deuteron. The results with/without theses tools are presented and their effect on the relevance of d-D sources versus d-Cu is evaluated

    Probing MHD Shocks with high-J CO observations: W28F

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    Context. Observing supernova remnants (SNRs) and modelling the shocks they are associated with is the best way to quantify the energy SNRs re-distribute back into the Interstellar Medium (ISM). Aims. We present comparisons of shock models with CO observations in the F knot of the W28 supernova remnant. These comparisons constitute a valuable tool to constrain both the shock characteristics and pre-shock conditions. Methods. New CO observations from the shocked regions with the APEX and SOFIA telescopes are presented and combined. The integrated intensities are compared to the outputs of a grid of models, which were combined from an MHD shock code that calculates the dynamical and chemical structure of these regions, and a radiative transfer module based on the 'large velocity gradient' (LVG) approximation. Results. We base our modelling method on the higher J CO transitions, which unambiguously trace the passage of a shock wave. We provide fits for the blue- and red-lobe components of the observed shocks. We find that only stationary, C-type shock models can reproduce the observed levels of CO emission. Our best models are found for a pre-shock density of 104 cm-3, with the magnetic field strength varying between 45 and 100 {\mu}G, and a higher shock velocity for the so-called blue shock (\sim25 km s-1) than for the red one (\sim20 km s-1). Our models also satisfactorily account for the pure rotational H2 emission that is observed with Spitzer.Comment: 8 pages, 6 figures, 1 table, accepted for A&A SOFIA/GREAT Special Issu

    Cool and warm dust emission from M33 (HerM33es)

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    We study the far-infrared emission from the nearby spiral galaxy M33 in order to investigate the dust physical properties such as the temperature and the luminosity density across the galaxy. Taking advantage of the unique wavelength coverage (100, 160, 250, 350 and 500 micron) of the Herschel Space Observatory and complementing our dataset with Spitzer-IRAC 5.8 and 8 micron and Spitzer-MIPS 24 and 70 micron data, we construct temperature and luminosity density maps by fitting two modified blackbodies of a fixed emissivity index of 1.5. We find that the 'cool' dust grains are heated at temperatures between 11 and 28 K with the lowest temperatures found in the outskirts of the galaxy and the highest ones in the center and in the bright HII regions. The infrared/submillimeter total luminosity (5 - 1000 micron) is estimated to be 1.9x10^9 Lsun. 59% of the total luminosity of the galaxy is produced by the 'cool' dust grains (~15 K) while the rest 41% is produced by 'warm' dust grains (~55 K). The ratio of the cool-to-warm dust luminosity is close to unity (within the computed uncertainties), throughout the galaxy, with the luminosity of the cool dust being slightly enhanced in the center of the galaxy. Decomposing the emission of the dust into two components (one emitted by the diffuse disk of the galaxy and one emitted by the spiral arms) we find that the fraction of the emission in the disk in the mid-infrared (24 micron) is 21%, while it gradually rises up to 57% in the submillimeter (500 micron). We find that the bulk of the luminosity comes from the spiral arm network that produces 70% of the total luminosity of the galaxy with the rest coming from the diffuse dust disk. The 'cool' dust inside the disk is heated at a narrow range of temperatures between 18 and 15 K (going from the center to the outer parts of the galaxy).Comment: 12 pages, 14 figures, accepted for publication in A&

    PACS and SPIRE photometer maps of M33: First results of the Herschel M33 extended survey (HERM33ES)

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    Within the framework of the HERM33ES key project, we are studying the star forming interstellar medium in the nearby, metal-poor spiral galaxy M33, exploiting the high resolution and sensitivity of Herschel. We use PACS and SPIRE maps at 100, 160, 250, 350, and 500 micron wavelength, to study the variation of the spectral energy distributions (SEDs) with galacto-centric distance. Detailed SED modeling is performed using azimuthally averaged fluxes in elliptical rings of 2 kpc width, out to 8 kpc galacto-centric distance. Simple isothermal and two-component grey body models, with fixed dust emissivity index, are fitted to the SEDs between 24 and 500 micron using also MIPS/Spitzer data, to derive first estimates of the dust physical conditions. The far-infrared and submillimeter maps reveal the branched, knotted spiral structure of M33. An underlying diffuse disk is seen in all SPIRE maps (250-500 micron). Two component fits to the SEDs agree better than isothermal models with the observed, total and radially averaged flux densities. The two component model, with beta fixed at 1.5, best fits the global and the radial SEDs. The cold dust component clearly dominates; the relative mass of the warm component is less than 0.3% for all the fits. The temperature of the warm component is not well constrained and is found to be about 60K plus/minus 10K. The temperature of the cold component drops significantly from about 24K in the inner 2 kpc radius to 13K beyond 6 kpc radial distance, for the best fitting model. The gas-to-dust ratio for beta=1.5, averaged over the galaxy, is higher than the solar value by a factor of 1.5 and is roughly in agreement with the subsolar metallicity of M33.Comment: 5 pages, 3 figures, accepted for publication in the A&A Herschel Special Issu

    Caveolin-1 protects B6129 mice against Helicobacter pylori gastritis.

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    Caveolin-1 (Cav1) is a scaffold protein and pathogen receptor in the mucosa of the gastrointestinal tract. Chronic infection of gastric epithelial cells by Helicobacter pylori (H. pylori) is a major risk factor for human gastric cancer (GC) where Cav1 is frequently down-regulated. However, the function of Cav1 in H. pylori infection and pathogenesis of GC remained unknown. We show here that Cav1-deficient mice, infected for 11 months with the CagA-delivery deficient H. pylori strain SS1, developed more severe gastritis and tissue damage, including loss of parietal cells and foveolar hyperplasia, and displayed lower colonisation of the gastric mucosa than wild-type B6129 littermates. Cav1-null mice showed enhanced infiltration of macrophages and B-cells and secretion of chemokines (RANTES) but had reduced levels of CD25+ regulatory T-cells. Cav1-deficient human GC cells (AGS), infected with the CagA-delivery proficient H. pylori strain G27, were more sensitive to CagA-related cytoskeletal stress morphologies ("humming bird") compared to AGS cells stably transfected with Cav1 (AGS/Cav1). Infection of AGS/Cav1 cells triggered the recruitment of p120 RhoGTPase-activating protein/deleted in liver cancer-1 (p120RhoGAP/DLC1) to Cav1 and counteracted CagA-induced cytoskeletal rearrangements. In human GC cell lines (MKN45, N87) and mouse stomach tissue, H. pylori down-regulated endogenous expression of Cav1 independently of CagA. Mechanistically, H. pylori activated sterol-responsive element-binding protein-1 (SREBP1) to repress transcription of the human Cav1 gene from sterol-responsive elements (SREs) in the proximal Cav1 promoter. These data suggested a protective role of Cav1 against H. pylori-induced inflammation and tissue damage. We propose that H. pylori exploits down-regulation of Cav1 to subvert the host's immune response and to promote signalling of its virulence factors in host cells

    CSF SerpinA1 in Creutzfeldt\u2013Jakob disease and frontotemporal lobar degeneration

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    Objective: SerpinA1 (alpha-1 antitrypsin) is an acute inflammatory protein, which seems to play a role in neurodegeneration and neuroinflammation. In Alzheimer\u2019s disease and synucleinopathies, SerpinA1 is overexpressed in the brain and the cerebrospinal fluid (CSF) showing abnormal patterns of its charge isoforms. To date, no comprehensive studies explored SerpinA1 CSF isoforms in Creutzfeldt\u2013Jakob disease (CJD) and frontotemporal lobar degeneration (FTLD). Methods: Using a capillary isoelectric focusing immunoassay, we analyzed CSF SerpinA1 isoforms in control cases (n = 31) and patients with a definite or probable diagnosis of CJD (n=77) or FTLD (n = 30), belonging to several disease subtypes. Results: The overall SerpinA1 signal was significantly higher than in controls in CJD subtypes linked to abnormal prion protein (PrPSc) type 1, such as sporadic CJD (sCJD) MM(V)1, and in FTLD-TDP. Moreover, CJD linked to PrPSc type 1 and FTLD-TAU groups showed a significant relative increase of acidic and basic isoforms in comparison with controls, thereby forming two distinct SerpinA1 isoform profiles. Interpretation: CJD linked to PrPSc type 1 and FTLD show a differential upregulation and post-translational modifications of CSF SerpinA1. Further studies are needed to clarify whether these findings may reflect a common, albeit disease-specific, pathogenetic mechanism related to neurodegeneration

    VizieR Online Data Catalog: Glycolaldehyde in Perseus young solar analogs (De Simone+, 2017)

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    Glycolaldehyde spatial distributions towards NGC1333-IRAS2A1, NGC1333-IRAS4A, NGC1333-IRAS4B1, and NGC1333 SVS13-A. The glycolaldehyde distribution refers to (1) the sum of the 76,2-65,1 and 76,1-65,2 emission with (220.2GHz, Eu=37K), and (2) the 222,21-211,20 emission (232.3GHz, Eu=135K). (2 data files). <P /

    Neurofilaments and progranulin are related to atrophy in frontotemporal lobar degeneration – A transdiagnostic study cross‐validating atrophy and fluid biomarkers

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    Introduction: Frontotemporal lobar degeneration (FTLD) encompasses behavioral variant frontotemporal dementia (bvFTD), progressive supranuclear palsy, corticobasal syndrome/degeneration, and primary progressive aphasias (PPAs). We cross-validated fluid biomarkers and neuroimaging.Methods: Seven fluid biomarkers from cerebrospinal fluid and serum were related to atrophy in 428 participants including these FTLD subtypes, logopenic variant PPA (lvPPA), Alzheimer's disease (AD), and healthy subjects. Atrophy was assessed by structural magnetic resonance imaging and atlas-based volumetry.Results: FTLD subtypes, lvPPA, and AD showed specific profiles for neurofilament light chain, phosphorylated heavy chain, tau, phospho-tau, amyloid beta1-42 from serum/cerebrospinal fluid, and brain atrophy. Neurofilaments related to regional atrophy in bvFTD, whereas progranulin was associated with atrophy in semantic variant PPA. Ubiquitin showed no effects.Discussion: Results specify biomarker and atrophy patterns in FTLD and AD supporting differential diagnosis. They identify neurofilaments and progranulin in interaction with structural imaging as promising candidates for monitoring disease progression and therapy.Highlights: Study cross-validated neuroimaging and fluid biomarkers in dementia. Five kinds of frontotemporal lobar degeneration and two variants of Alzheimer's disease. Study identifies disease-specific fluid biomarker and atrophy profiles. Fluid biomarkers and atrophy interact in a disease-specific way. Neurofilaments and progranulin are proposed as biomarkers for diagnosis and therapy
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