Cosmologically allowed regions for the axion decay constant FaF_a

If the Peccei-Quinn symmetry is already broken during inflation, the decay constant $F_a$ of the axion can be in a wide region from $10^{11}$ GeV to $10^{18}$ GeV for the axion being the dominant dark matter. In this case, however, the axion causes the serious cosmological problem, isocurvature perturbation problem, which severely constrains the Hubble parameter during inflation. The constraint is relaxed when Peccei-Quinn scalar field takes a large value $\sim M_{p}$ (Planck scale) during inflation. In this letter, we point out that the allowed region of the decay constant $F_a$ is reduced to a rather narrow region for a given tensor-to-scalar ratio $r$ when Peccei-Quinn scalar field takes $\sim M_{p}$ during inflation. For example, if the ratio $r$ is determined as $r \gtrsim 10^{-3}$ in future measurements, we can predict $F_a \simeq (0.1-1.4)\times 10^{12}$ GeV for domain wall number $N_\text{DW}=6$.Comment: 9 pages, 1 figure, LaTeX; some explanations and references adde

Fast ignitor research at the Institute of Laser Engineering, Osaka University

Copyright 2001 American Institute of Physics. This article may be downloaded for personal use only. Any other use requires prior permission of the author and the American Institute of Physics. The following article appeared in Physics of Plasmas, 8(5), 2268-2274, 2001 and may be found at http://dx.doi.org/10.1063/1.135259

Studies of ultra-intense laser plasma interactions for fast ignition

Copyright 2000 American Institute of Physics. This article may be downloaded for personal use only. Any other use requires prior permission of the author and the American Institute of Physics. The following article appeared in Physics of Plasmas, 7(5), 2014-2022, 2000 and may be found at http://dx.doi.org/10.1063/1.87402

Medium-size-vessel vasculitis

Medium-size-artery vasculitides do occur in childhood and manifest, in the main, as polyarteritis nodosa (PAN), cutaneous PAN and Kawasaki disease. Of these, PAN is the most serious, with high morbidity and not inconsequential mortality rates. New classification criteria for PAN have been validated that will have value in epidemiological studies and clinical trials. Renal involvement is common and recent therapeutic advances may result in improved treatment options. Cutaneous PAN is a milder disease characterised by periodic exacerbations and often associated with streptococcal infection. There is controversy as to whether this is a separate entity or part of the systemic PAN spectrum. Kawasaki disease is an acute self-limiting systemic vasculitis, the second commonest vasculitis in childhood and the commonest cause of childhood-acquired heart disease. Renal manifestations occur and include tubulointerstitial nephritis and renal failure. An infectious trigger and a genetic predisposition seem likely. Intravenous immunoglobulin (IV-Ig) and aspirin are effective therapeutically, but in resistant cases, either steroid or infliximab have a role. Greater understanding of the pathogenetic mechanisms involved in these three types of vasculitis and better long-term follow-up data will lead to improved therapy and prediction of prognosis