48 research outputs found
Polarimetry of binary systems: polars, magnetic CVs, XRBs
Polarimetry provides key physical information on the properties of
interacting binary systems, sometimes difficult to obtain by any other type of
observation. Indeed, radiation processes such as scattering by free electrons
in the hot plasma above accretion discs, cyclotron emission by mildly
relativistic electrons in the accretion shocks on the surface of highly
magnetic white dwarfs and the optically thin synchrotron emission from jets can
be observed. In this review, I will illustrate how optical/near-infrared
polarimetry allows one to estimate magnetic field strengths and map the
accretion zones in magnetic Cataclysmic Variables as well as determine the
location and nature of jets and ejection events in X-ray binaries.Comment: 26 pages, 16 figures; to be published in Astrophysics and Space
Science Library 460, Astronomical Polarisation from the Infrared to Gamma
Rays, Editors: Mignani, R., Shearer, A., S{\l}owikowska, A., Zane,
Measurement of the Ratio of b Quark Production Cross Sections in Antiproton-Proton Collisions at 630 GeV and 1800 GeV
We report a measurement of the ratio of the bottom quark production cross
section in antiproton-proton collisions at 630 GeV to 1800 GeV using bottom
quarks with transverse momenta greater than 10.75 GeV identified through their
semileptonic decays and long lifetimes. The measured ratio
sigma(630)/sigma(1800) = 0.171 +/- .024 +/- .012 is in good agreement with
next-to-leading order (NLO) quantum chromodynamics (QCD)
Seipin and the membrane-shaping protein Pex30 cooperate in organelle budding from the endoplasmic reticulum
Lipid droplets (LDs) and peroxisomes are ubiquitous organelles with central roles in eukaryotic cells. Although the mechanisms involved in biogenesis of these organelles remain elusive, both seem to require the endoplasmic reticulum (ER). Here we show that in yeast the ER budding of these structurally unrelated organelles has remarkably similar requirements and involves cooperation between Pex30 and the seipin complex. In the absence of these components, budding of both LDs and peroxisomes is inhibited, leading to the ER accumulation of their respective constituent molecules, such as triacylglycerols and peroxisomal membrane proteins, whereas COPII vesicle formation remains unaffected. This phenotype can be reversed by remodeling ER phospholipid composition highlighting a key function of these lipids in organelle biogenesis. We propose that seipin and Pex30 act in concert to organize membrane domains permissive for organelle budding, and that may have a lipid composition distinct from the bulk ER