26 research outputs found

    A Far-Ultraviolet View of Starburst Galaxies

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    Recent observational and theoretical results on starburst galaxies related to the wavelength regime below 1200 A are discussed. The review covers stars, dust, as well as hot and cold gas. This wavelength region follows trends similar to those seen at longer wavelengths, with several notable exceptions. Even the youngest stellar populations show a turn-over in their spectral energy distributions, and line-blanketing is much more pronounced. Furthermore, the O VI line allows one to probe gas at higher temperatures than possible with lines at longer wavelengths. Molecular hydrogen lines (if detected) provide a glimpse of the cold phase. I cover the crucial wavelength regime below 912 A and the implications of recent attempts to detect the escaping ionizing radiation.Comment: 8 pages, 3 figures, Invited Talk, Starbursts--From 30 Doradus to Lyman-Break Galaxies, ed. R. de Grijs & R. M. Gonzalez Delgado (Dordrecht: Kluwer

    Analysing the elasticity difference tensor of general relativity

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    The elasticity difference tensor, used in [1] to describe elasticity properties of a continuous medium filling a space-time, is here analysed from the point of view of the space-time connection. Principal directions associated with this tensor are compared with eigendirections of the material metric. Examples concerning spherically symmetric and axially symmetric space-times are then presented.Comment: 17 page

    Fitting the integrated Spectral Energy Distributions of Galaxies

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    Fitting the spectral energy distributions (SEDs) of galaxies is an almost universally used technique that has matured significantly in the last decade. Model predictions and fitting procedures have improved significantly over this time, attempting to keep up with the vastly increased volume and quality of available data. We review here the field of SED fitting, describing the modelling of ultraviolet to infrared galaxy SEDs, the creation of multiwavelength data sets, and the methods used to fit model SEDs to observed galaxy data sets. We touch upon the achievements and challenges in the major ingredients of SED fitting, with a special emphasis on describing the interplay between the quality of the available data, the quality of the available models, and the best fitting technique to use in order to obtain a realistic measurement as well as realistic uncertainties. We conclude that SED fitting can be used effectively to derive a range of physical properties of galaxies, such as redshift, stellar masses, star formation rates, dust masses, and metallicities, with care taken not to over-interpret the available data. Yet there still exist many issues such as estimating the age of the oldest stars in a galaxy, finer details ofdust properties and dust-star geometry, and the influences of poorly understood, luminous stellar types and phases. The challenge for the coming years will be to improve both the models and the observational data sets to resolve these uncertainties. The present review will be made available on an interactive, moderated web page (sedfitting.org), where the community can access and change the text. The intention is to expand the text and keep it up to date over the coming years.Comment: 54 pages, 26 figures, Accepted for publication in Astrophysics & Space Scienc

    A surface plasmon resonance-based solution affinity assay for heparan sulfate-binding proteins

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    A surface plasmon resonance-based solution affinity assay is described for measuring the Kd of binding of heparin/heparan sulfate-binding proteins with a variety of ligands. The assay involves the passage of a pre-equilibrated solution of protein and ligand over a sensor chip onto which heparin has been immobilised. Heparin sensor chips prepared by four different methods, including biotin–streptavidin affinity capture and direct covalent attachment to the chip surface, were successfully used in the assay and gave similar Kd values. The assay is applicable to a wide variety of heparin/HS-binding proteins of diverse structure and function (e.g., FGF-1, FGF-2, VEGF, IL-8, MCP-2, ATIII, PF4) and to ligands of varying molecular weight and degree of sulfation (e.g., heparin, PI-88, sucrose octasulfate, naphthalene trisulfonate) and is thus well suited for the rapid screening of ligands in drug discovery applications
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