Star clusters as building blocks for dSph galaxies formation

We study numerically the formation of dSph galaxies. Intense star bursts, e.g. in gas-rich environments, typically produce a few to a few hundred young star clusters, within a region of just a few hundred pc. The dynamical evolution of these star clusters may explain the formation of the luminous component of dwarf spheroidal galaxies (dSph). Here we perform a numerical experiment to show that the evolution of star clusters complexes in dark matter haloes can explain the formation of the luminous components of dSph galaxies.Comment: 4 pages, 4 figures, Proceedings of IAU symposium 266 'Star Clusters - Basic Building Blocks

A Possible Formation Scenario for Dwarf Spheroidal Galaxies - II: A Parameter Study

Dwarf spheroidal (dSph) galaxies are considered the basic building blocks of the galaxy formation process in the LCDM (Lambda Cold Dark Matter) hierarchical cosmological model. These galaxies are believed to be the most dark matter (DM) dominated systems known, have the lowest stellar content, and are poor in gas. Many theories attempt to explain the formation of dSph galaxies resorting to the fact that these galaxies are mainly found orbiting large galaxies or invoking other mechanisms of interactions. Here we show the full set of simulation as an extension of our fiducial model, where we study the formation of classical dSph galaxies in isolation by dissolving star clusters within the DM halo of the dwarf galaxy. In our parameter survey we adopt cored and cusped DM halo profiles and consider different numbers of dissolving star clusters. We investigate the dependency of observable quantities with different masses and scale-lengths of the DM halo and different star formation efficiencies (SFE). We find that our proposed scenario explains many features of the classical dSph galaxies of the Milky Way, like their morphology and their dynamics. We see trends how the surface brightness and the scale-length of the luminous component vary with the parameters of our simulations. We also identify how irregularities in their shape, i.e. clumpiness and ellipticity vary in our simulations. In velocity space, we identify the parameters leading to flat velocity dispersions curves. We recognize kinematically cold substructures in velocity space, named fossil remnants and stemming from our unique initial conditions, which alter the expected results. These streaming motions are considered as a key feature for future observation with high resolution to validate our scenario.Comment: 23 pages, 9 figures, 4 Tables, accepted for publication in MNRA

Chemical defenses of the Caribbean sponges Agelas wiedenmayeri and Agelas conifera

Previous studies have determined that Caribbean reef sponges of the genus Agelas are chemically defended from fish predation by brominated pyrrole alkaloids, and that the compounds responsible for this defense have been elucidated for one species, Agelas clathrodes. In this study, we expand our understanding of chemical defense in this common sponge genus to include the characterization of defensive metabolites in the tissues of Agelas wiedenmayeri and Agelas conifera. Bioassay-directed isolation of defensive metabolites was undertaken using fish feeding assays carried out in laboratory aquaria and in the field. Agelas wiedenmayeri contained the same two major metabolites as Agelas clathrodes, 4,5-dibromopyrrole-2-carboxylic acid (1), and oroidin (2), in addition to a small amount of bromoageliferin (7). The two major metabolites were present at higher concentrations in samples of Agelas wiedenmayeri than in Agelas clathrodes, and their relative concentrations were reversed, with Agelas wiedenmayeri on average containing more 4,5-dibromopyrrole-2-carboxylic acid (1) (2.0 mg/mL) than oroidin (2) (0.8 mg/mL). Agelas conifera contained a mixture of dimeric bromopyrrole alkaloids dominated by sceptrin (3), with <10% each of dibromosceptrin (5), bromoageliferin (7), dibromoageliferin (8), ageliferin (6), and bromosceptrin (4). Mean concentration of sceptrin (3) in sponge tissue was 5.3 mg/mL; this compound deterred feeding of reef fish in aquarium assays at 1.0 mg/mL, the lowest concentration assayed. Sceptrin (3) concentrations were higher in sponges collected in the southern Bahama Islands than those collected in the middle Bahamas, but reasons for this variation remain unclear. The structure-activity relationship of the pyrrole group was investigated by assaying derivatives of the active metabolites. Feeding deterrent activity of the molecule was enhanced by the addition of bromine to the pyrrole group, but not affected by exchange of the heteroatom from N to O or S. Combining an understanding of the structure-activity relationship of Agelas metabolites with an understanding of the variation in these metabolites across the genus may provide insight into the evolution of defensive chemistry in this highly successful taxa of pan-tropical sponges

Measurements of heavy ion beam losses from collimation

The collimation efficiency for Pb ion beams in the LHC is predicted to be lower than requirements. Nuclear fragmentation and electromagnetic dissociation in the primary collimators create fragments with a wide range of Z/A ratios, which are not intercepted by the secondary collimators but lost where the dispersion has grown sufficiently large. In this article we present measurements and simulations of loss patterns generated by a prototype LHC collimator in the CERN SPS. Measurements were performed at two different energies and angles of the collimator. We also compare with proton loss maps and find a qualitative difference between Pb ions and protons, with the maximum loss rate observed at different places in the ring. This behavior was predicted by simulations and provides a valuable benchmark of our understanding of ion beam losses caused by collimation.Comment: 12 pages, 20 figure

Membranous glomerulonephritis in the mouse

Membranous glomerulonephritis in the mouse. Glomerulonephritis was induced in C57.B110 mice by a single injection of rabbit IgG against homologous, pronase-digested, renal tubular antigens. The heterologous phase was characterized by a transient increase of glomerular permeability with fixation of rabbit IgG to the capillary walls, in a linear or fine-granular pattern, and to the brush borders of the proximal tubuli. The autologous phase was marked by the immune response to the injected protein, during which subepithelial immune deposits, consisting of mouse IgG1, rabbit IgG, and mouse C3 developed. Small amounts were still present at 1 year after the injection of antiserum. The antibody response of the mice correlated with the development and resolution of the deposits. None of the mice developed a nephrotic syndrome. Control mice treated with normal rabbit IgG did not show immune deposits in their kidneys at any stage despite a comparable antibody response to rabbit IgG. Immunoelectronmicroscopy showed that the rabbit antibodies fixed directly to an antigen in the cell membrane of the glomerular visceral epithelium. It seems, therefore, likely that in situ formation of subepithelial immune complexes occurred in the autologous phase by fixation of mouse immunoglobulins to rabbit IgG already present in the glomerular wall.Glomérulonéphrite extra-membraneuse chez la souris. Une glomérulonéphrite a été induite chez des souris C57.B110 par une injection unique d'IgG de lapin contre des antigènes tubulaires rénaux homologues, digérés par de la pronase. La phase hétérologue était caractérisée par une augmentation transitoire de la perméabilité glomérulaire avec fixation d'IgG de lapin aux parois capillaires, d'une façon linéaire ou finement granuleuse, et aux bordures en brosse des tubules proximaux. La phase autologue était marquée par la réponse immune à la protéine injectée, pendant laquelle des dépôts immuns sous-épithéliaux, consistant en de l'IgG1 de souris, de l'IgG de lapin et du C3 de souris, se sont développés. Il en restait encore de faibles quantités 1 an après l'injection de l'antisérum. La réponse anticorps des souris était corrélée avec le développement et la disparition des dépôts. Aucune des souris n'a développé de syndrome néphrotique. Les souris contrôles traitées avec de l'IgG de lapin normal n'ont pas eu de dépôts immuns dans le rein à aucun stade, malgré une réponse anticorps aux IgG de lapin comparable. La microscopie immuno-électronique a montré que les anticorps de lapin se fixaient directement à un antigène situé sur la membrane des cellules de l'épithélium viscéral glomérulaire. Il semble donc probable que la formation in situ de complexes immuns sous-épithéliaux est survenue à la phase autologue par fixation d'immunoglobulines de souris à de l'IgG de lapin déjà présente dans la paroi glomérulaire