6,365 research outputs found
The Discovery of an X-ray/UV Stellar Flare from the Late-K/Early-M Dwarf LMC 335
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
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
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 , where n
varies from 47 to 59 and for , 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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Room temperature "optical nanodiamond hyperpolarizer": Physics, design, and operation.
Dynamic Nuclear Polarization (DNP) is a powerful suite of techniques that deliver multifold signal enhancements in nuclear magnetic resonance (NMR) and MRI. The generated athermal spin states can also be exploited for quantum sensing and as probes for many-body physics. Typical DNP methods require the use of cryogens, large magnetic fields, and high power microwave excitation, which are expensive and unwieldy. Nanodiamond particles, rich in Nitrogen-Vacancy (NV) centers, have attracted attention as alternative DNP agents because they can potentially be optically hyperpolarized at room temperature. Here, unraveling new physics underlying an optical DNP mechanism first introduced by Ajoy et al. [Sci. Adv. 4, eaar5492 (2018)], we report the realization of a miniature "optical nanodiamond hyperpolarizer," where 13C nuclei within the diamond particles are hyperpolarized via the NV centers. The device occupies a compact footprint and operates at room temperature. Instrumental requirements are very modest: low polarizing fields, low optical and microwave irradiation powers, and convenient frequency ranges that enable miniaturization. We obtain the best reported optical 13C hyperpolarization in diamond particles exceeding 720 times of the thermal 7 T value (0.86% bulk polarization), corresponding to a ten-million-fold gain in averaging time to detect them by NMR. In addition, the hyperpolarization signal can be background-suppressed by over two-orders of magnitude, retained for multiple-minute long periods at low fields, and deployed efficiently even to 13C enriched particles. Besides applications in quantum sensing and bright-contrast MRI imaging, this work opens possibilities for low-cost room-temperature DNP platforms that relay the 13C polarization to liquids in contact with the high surface-area particles
Light particle spectra from 35 MeV/nucleon 12C-induced reactions on 197Au
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
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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