6,365 research outputs found

    The Discovery of an X-ray/UV Stellar Flare from the Late-K/Early-M Dwarf LMC 335

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    We report the discovery of an X-ray/UV stellar flare from the source LMC 335, captured by XMM-Newton in the field of the Large Magellanic Cloud. The flare event was recorded continuously in X-ray for its first 10 hours from the precursor to the late decay phases. The observed fluxes increased by more than two orders of magnitude at its peak in X-ray and at least one in the UV as compared to quiescence. The peak 0.1-7.0 keV X-ray flux is derived from the two-temperature APEC model to be ~(8.4 +/- 0.6) x 10^-12 erg cm-2 s-1. Combining astrometric information from multiple X-ray observations in the quiescent and flare states, we identify the NIR counterpart of LMC 335 as the 2MASS source J05414534-6921512. The NIR color relations and spectroscopic parallax characterize the source as a Galactic K7-M4 dwarf at a foreground distance of (100 - 264) pc, implying a total energy output of the entire event of ~(0.4 - 2.9) x 10^35 erg. This report comprises detailed analyses of this late-K / early-M dwarf flare event that has the longest time coverage yet reported in the literature. The flare decay can be modeled with two exponential components with timescales of ~28 min and ~4 hours, with a single component decay firmly ruled out. The X-ray spectra during flare can be described by two components, a dominant high temperature component of ~40-60MK and a low temperature component of ~10MK, with a flare loop length of about 1.1-1.3 stellar radius.Comment: 35 pages, 6 figures, 5 tables, accepted for publication in Ap

    Nuclear isotope thermometry

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    We discuss different aspects which could influence temperatures deduced from experimental isotopic yields in the multifragmentation process. It is shown that fluctuations due to the finite size of the system and distortions due to the decay of hot primary fragments conspire to blur the temperature determination in multifragmentation reactions. These facts suggest that caloric curves obtained through isotope thermometers, which were taken as evidence for a first-order phase transition in nuclear matter, should be investigated very carefully.Comment: 9 pages, 7 figure

    Effect of isospin dependent cross-section on fragment production in the collision of charge asymmetric nuclei

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    To understand the role of isospin effects on fragmentation due to the collisions of charge asymmetric nuclei, we have performed a complete systematical study using isospin dependent quantum molecular dynamics model. Here simulations have been carried out for 124Xn+124Xn^{124}X_{n}+ ^{124}X_{n}, where n varies from 47 to 59 and for 40Ym+40Ym^{40}Y_{m}+ ^{40}Y_{m}, where m varies from 14 to 23. Our study shows that isospin dependent cross-section shows its influence on fragmentation in the collision of neutron rich nuclei

    Upper airway change after oral appliance in obstructive sleep apnoea patients - difference exist in good and poor responders

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    Light particle spectra from 35 MeV/nucleon 12C-induced reactions on 197Au

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    Energy spectra for p, d, t, 3He, 4He, and 6He from the reaction 12C+197Au at 35 MeV/nucleon are presented. A common intermediate rapidity source is identified using a moving source fit to the spectra that yields cross sections which are compared to analogous data at other bombarding energies and to several different models. The excitation function of the composite to proton ratios is compared with quantum statistical, hydrodynamic, and thermal models

    CD4+ T-cell responses to Epstein-Barr virus nuclear antigen EBNA1 in Chinese populations are highly focused on novel C-terminal domain-derived epitopes

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    Epstein-Barr virus nuclear antigen EBNA1, the one viral protein uniformly expressed in nasopharyngeal carcinoma (NPC), represents a prime target for T-cell-based immunotherapy. However, little is known about the EBNA1 epitopes, particularly CD4 epitopes, presented by HLA alleles in Chinese people, the group at highest risk for NPC. We analyzed the CD4+^+ T-cell responses to EBNA1 in 78 healthy Chinese donors and found marked focusing on a small number of epitopes in the EBNA1 C-terminal region, including a DP5- restricted epitope that was recognized by almost half of the donors tested and elicited responses able to recognize EBNA1-expressing, DP5-positive target cells
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