Dynamic Power Spectral Analysis of Solar Measurements from Photospheric, Chromospheric, and Coronal Sources

An important aspect in the power spectral analysis of solar variability is the quasistationary and quasiperiodic nature of solar periodicities. In other words, the frequency, phase, and amplitude of solar periodicities vary on time scales ranging from active region lifetimes to solar cycle time scales. Here, researchers employ a dynamic, or running, power spectral density analysis to determine many periodicities and their time-varying nature in the projected area of active sunspot groups (S sub act). The Solar Maximum Mission/Active Cavity Radiometer Irradiance Monitor (SMM/ACRIM) total solar irradiance (S), the Nimbus-7 MgII center-to-wing ratio (R (MgII sub c/w)), the Ottawa 10.7 cm flux (F sub 10.7), and the GOES background x ray flux (X sub b) for the maximum, descending, and minimum portions of solar cycle 21 (i.e., 1980 to 1986) are used. The technique dramatically illustrates several previously unrecognized periodicities. For example, a relatively stable period at about 51 days has been found in those indices which are related to emerging magnetic fields. The majority of solar periodicities, particularly around 27, 150 and 300 days, are quasiperiodic because they vary in amplitude and frequency throughout the solar cycle. Finally, it is shown that there are clear differences between the power spectral densities of solar measurements from photospheric, chromospheric, and coronal sources

Observed solar near UV variability: A contribution to variations of the solar constant

Continuous Measurements of the Solar UV have been made by an instrument on the Solar Mesosphere Explorer (SME) since October 1981. The results for the wavelength interval 200 to 300 nm show an irradiance decrease to a minimum in early 1987 and a subsequent increase to mid-April 1989. The observed UV changes during part of solar cycles 21 to 22 represent approx. 35 percent (during the decreasing phase) and 25 percent (during the increasing phase) of the observed variations of the solar constant for the same time period as the SME measurements

Widespread occurrence of Mycobacterium tuberculosis DNA from 18th-19th century Hungarians

A large number (265) of burials from 1731-1838 were discovered in sealed crypts of the Dominican Church, Vac, Hungary in 1994. Many bodies were naturally mummified, so that both soft tissues and bones were available. Contemporary archives enabled the determination of age at death, and the identification of family groups. In some cases, symptoms before death were described and, occasionally, occupation. Initial radiological examination of a small number of individuals had indicated calcified lung lesions and demonstrable acid-fast bacteria suggestive of tuberculosis infection. Tuberculosis was endemic in 18th-19th century Europe, so human remains should contain detectable Mycobacterium tuberculosis complex (MTB) DNA, enabling comparisons with modern isolates. Therefore, a comprehensive examination of 168 individuals for the presence of MTB DNA was undertaken. Specific DNA amplification methods for MTB showed that 55% of individuals were positive and that the incidence varied according to age at death and sampling site in the body. Radiographs were obtained from 27 individuals and revealed an association between gross pathology and the presence of MTB DNA. There was an inverse relationship between PCR positivity and MTB target sequence size. In some cases, the preservation of MTB DNA was excellent, and several target gene sequences could be detected from the same sample. This information, combined with MTB DNA sequencing data and molecular typing techniques, will enable us to study the past epidemiology of TB infection, and extends the timeframe for studying changes in molecular fingerprints. Am J Phys Anthropol 120:144-152, 2003. (C) 2003 Wiley-Liss, Inc

Modeling Solar Lyman Alpha Irradiance

Solar Lyman alpha irradiance is estimated from various solar indices using linear regression analyses. Models developed with multiple linear regression analysis, including daily values and 81-day running means of solar indices, predict reasonably well both the short- and long-term variations observed in Lyman alpha. It is shown that the full disk equivalent width of the He line at 1083 nm offers the best proxy for Lyman alpha, and that the total irradiance corrected for sunspot effect also has a high correlation with Lyman alpha

Numerical study of SU(2) Yang-Mills theory with gluinos

We report on a numerical investigation of the SU(2) gauge theory with gluinos. The low-lying spectrum in bosonic and fermionic channels is determined. Improvements of the multi-bosonic algorithm are discussed.Comment: latex, 3 pages, 4 figures; Poster presented by K. Spanderen at LATTICE9

Antibody-mediated inhibition of syndecan-4 dimerisation reduces interleukin (IL)-1 receptor trafficking and signalling.

OBJECTIVE: Syndecan-4 (sdc4) is a cell-anchored proteoglycan that consists of a transmembrane core protein and glucosaminoglycan (GAG) side chains. Binding of soluble factors to the GAG chains of sdc4 may result in the dimerisation of sdc4 and the initiation of downstream signalling cascades. However, the question of how sdc4 dimerisation and signalling affects the response of cells to inflammatory stimuli is unknown. METHODS: Sdc4 immunostaining was performed on rheumatoid arthritis (RA) tissue sections. Interleukin (IL)-1 induced extracellular signal-regulated kinases (ERK) phosphorylation and matrix metalloproteinase-3 production was investigated. Il-1 binding to sdc4 was investigated using immunoprecipitation. IL-1 receptor (IL1R1) staining on wild-type, sdc4 and IL1R1 knockout fibroblasts was performed in fluorescence-activated cell sorting analyses. A blocking sdc4 antibody was used to investigate sdc4 dimerisation, IL1R1 expression and the histological paw destruction in the human tumour necrosis factor-alpha transgenic mouse. RESULTS: We show that in fibroblasts, the loss of sdc4 or the antibody-mediated inhibition of sdc4 dimerisation reduces the cell surface expression of the IL-1R and regulates the sensitivity of fibroblasts to IL-1. We demonstrate that IL-1 directly binds to sdc4 and in an IL-1R-independent manner leads to its dimerisation. IL-1-induced dimerisation of sdc4 regulates caveolin vesicle-mediated trafficking of the IL1R1, which in turn determines the responsiveness to IL-1. Administration of antibodies (Ab) against the dimerisation domain of sdc4, thus, strongly reduces the expression IL1R1 on arthritic fibroblasts both in vitro and an animal model of human RA. CONCLUSION: Collectively, our data suggest that Ab that specifically inhibit sdc4 dimerisation may support anti-IL-1 strategies in diseases such as inflammatory arthritis