631 research outputs found

    Cluster Galaxy Evolution from a New Sample of Galaxy Clusters at 0.3 < z < 0.9

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    (Abridged) We analyze photometry and spectroscopy of a sample of 63 clusters at 0.3<z<0.9 drawn from the Las Campanas Distant Cluster Survey to empirically constrain models of cluster galaxy evolution. Specifically, by combining data on our clusters with those from the literature we parametrize the redshift dependence of 1) M*_I in the observed frame; 2) the V-I color of the E/S0 red sequence in the observed frames; and 3) the I-K' color of the E/S0 red sequence in the observed frame. Using the peak surface brightness of the cluster detection, S, as a proxy for cluster mass, we find no correlation between S and M* or the location of the red envelope in V-I. We suggest that these observations can be explained with a model in which luminous early type galaxies (or more precisely, the progenitors of current day luminous early type galaxies) form the bulk of their stellar populations at high redshift (>~ 5) and in which many of these galaxies, if not all, accrete mass either in the form of evolved stellar populations or gas that causes only a short term episode of star formation at lower redshifts (1.5 < z < 2). Our data are too crude to reach conclusions regarding the evolutionary state of any particular cluster or to investigate whether the morphological evolution of galaxies matches the simple scenario we discuss, but the statistical nature of this study suggests that the observed evolutionary trends are universal in massive clusters.Comment: 35 pages, accepted for publication in Ap

    Multiaperture UBVRIzJHKUBVRIzJHK Photometry of Galaxies in the Coma Cluster

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    We present a set of UBVRIzJHKsUBVRIzJHK_s photometry for 745 J+HJ+H band selected objects in a 22.5′×29.2′22.5' \times 29.2' region centered on the core of the Coma cluster. This includes 516 galaxies and is at least 80% complete to H=16, with a spectroscopically complete sample of 111 cluster members (nearly all with morphological classification) for H<14.5H < 14.5. For each object we present total \cite{kron80} magnitudes and aperture photometry. As an example, we use these data to derive color-magnitude relations for Coma early-type galaxies, measure the intrinsic scatter of these relations and its dependence on galaxy mass, and address the issue of color gradients. We find that the color gradients are mild and that the intrinsic scatter about the color-magnitude relation is small (∼0.05\sim 0.05 mag in U−VU-V and less than ∼0.03\sim 0.03 in B−RB-R, V−IV-I or J−KJ-K). There is no evidence that the intrinsic scatter varies with galaxy luminosity, suggesting that the cluster red sequence is established at early epochs over a range of ∼100\sim 100 in stellar mass.Comment: 41 pages, 5 figures, 18 data tables attached to source files or available on request from R. De propris. Accepted for publication in Astrophysical Journal Supplement Serie

    Revisiting Brightest Cluster Galaxy Evolution with the Las Campanas Distant Cluster Survey

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    We investigate the influence of environment on brightest cluster galaxy (BCG) evolution using a sample of 63 clusters at 0.3 < z < 0.9 drawn primarily from the Las Campanas Distant Cluster Survey and follow-up V, I, and K' photometry. The luminosity evolution of the entire BCG sample is not adequately described by a single evolutionary model. Using the integrated light from the cluster detection as a proxy for cluster Lx and the suggestion by Burke, Collins, & Mann, we set Lx = 2 x 10^{44} ergs/s to be the division between high and low luminosity clusters. At high redshift (z>0.6) BCGs from low-Lx clusters are fainter, on average, than those from high-Lx clusters and are best modeled as having constant luminosity with redshift. The BCGs from high-Lx cluster are best modeled as having a stellar population that formed at large redshift (z_form > 5) and is passively evolving. However, for the entire BCG population, the observed V-I and I-K' colors are well described by a single evolutionary model in which the stellar populations have z_form > 5 and subsequently passively evolve. We conclude that accretion is proportionally more significant for BCGs in lower mass clusters at these redshifts (factor of 2 to 4 increase in mass since z ~ 1 for the low Lx systems) and that the accreted matter is in the form of systems with evolved stellar populations.Comment: 32 pages (18 figures, 1 figure abridged for electronic version) Accepted for publication in Ap

    Reconstruction of the superior vena cava: Benefits of postoperative surveillance and secondary endovascular interventions

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    AbstractPurpose: Superior vena cava (SVC) reconstructions are rarely performed; therefore the need for surveillance and the results of secondary interventions are unknown. Methods: During a 14-year period 19 patients (11 male, 8 female; mean age 41.9 years, range 8 to 69 years) underwent SVC reconstruction for symptomatic nonmalignant disease. Causes included mediastinal fibrosis (n = 12), indwelling foreign bodies (n = 4), idiopathic thrombosis (n = 2), and antithrombin III deficiency (n = 1). Spiral saphenous vein graft (n = 14), polytetrafluoroethylene (n = 4), or human allograft (n = 1) was implanted. Results: No early death or pulmonary embolism occurred. Four early graft stenoses or thromboses (spiral saphenous vein graft, n = 2, polytetrafluoroethylene, n = 2) required thrombectomy, with success in three. During a mean follow-up of 49.5 months (range, 4.7 to 137 months), 95 imaging studies were performed (average, five per patient; range, one to 10 studies). Venography detected mild or moderate graft stenosis in seven patients; two progressed to severe stenosis. Two additional grafts developed early into severe stenosis. Four of 19 grafts occluded during follow-up (two polytetrafluoroethylene, two spiral saphenous vein graft). Computed tomography failed to identify stenosis in two grafts, magnetic resonance imaging failed to confirm one stenosis and one graft occlusion, and duplex scanning was inconclusive on graft patency in 10 patients. Angioplasty was performed in all four patients with severe stenosis, with simultaneous placement of Wallstents in two. One of the Wallstents occluded at 9 months. Repeat percutaneous transluminal angioplasty was necessary in two patients, with placement of Palmaz stents in one. Only one graft occlusion and one severe graft stenosis occurred beyond 1 year. The primary, primary-assisted, and secondary patency rates were 61%, 78%, and 83% at 1 year and 53%, 70%, and 74% at 5 years, respectively. Conclusions: Long-term secondary patency rates justify SVC grafting for benign disease. Postoperative surveillance with contrast venography is indicated in the first year to detect graft problems. Endovascular techniques may salvage and improve the patency of SVC grafts. (J Vasc Surg 1998;27:287-301.

    Precision Measurement of the Weak Mixing Angle in Moller Scattering

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    We report on a precision measurement of the parity-violating asymmetry in fixed target electron-electron (Moller) scattering: A_PV = -131 +/- 14 (stat.) +/- 10 (syst.) parts per billion, leading to the determination of the weak mixing angle \sin^2\theta_W^eff = 0.2397 +/- 0.0010 (stat.) +/- 0.0008 (syst.), evaluated at Q^2 = 0.026 GeV^2. Combining this result with the measurements of \sin^2\theta_W^eff at the Z^0 pole, the running of the weak mixing angle is observed with over 6 sigma significance. The measurement sets constraints on new physics effects at the TeV scale.Comment: 4 pages, 2 postscript figues, submitted to Physical Review Letter

    Iatrogenic air embolism: pathoanatomy, thromboinflammation, endotheliopathy, and therapies

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    Iatrogenic vascular air embolism is a relatively infrequent event but is associated with significant morbidity and mortality. These emboli can arise in many clinical settings such as neurosurgery, cardiac surgery, and liver transplantation, but more recently, endoscopy, hemodialysis, thoracentesis, tissue biopsy, angiography, and central and peripheral venous access and removal have overtaken surgery and trauma as significant causes of vascular air embolism. The true incidence may be greater since many of these air emboli are asymptomatic and frequently go undiagnosed or unreported. Due to the rarity of vascular air embolism and because of the many manifestations, diagnoses can be difficult and require immediate therapeutic intervention. An iatrogenic air embolism can result in both venous and arterial emboli whose anatomic locations dictate the clinical course. Most clinically significant iatrogenic air emboli are caused by arterial obstruction of small vessels because the pulmonary gas exchange filters the more frequent, smaller volume bubbles that gain access to the venous circulation. However, there is a subset of patients with venous air emboli caused by larger volumes of air who present with more protean manifestations. There have been significant gains in the understanding of the interactions of fluid dynamics, hemostasis, and inflammation caused by air emboli due to in vitro and in vivo studies on flow dynamics of bubbles in small vessels. Intensive research regarding the thromboinflammatory changes at the level of the endothelium has been described recently. The obstruction of vessels by air emboli causes immediate pathoanatomic and immunologic and thromboinflammatory responses at the level of the endothelium. In this review, we describe those immunologic and thromboinflammatory responses at the level of the endothelium as well as evaluate traditional and novel forms of therapy for this rare and often unrecognized clinical condition

    SARS Surveillance during Emergency Public Health Response, United States, March–July 2003

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    In response to the emergence of severe acute respiratory syndrome (SARS), the United States established national surveillance using a sensitive case definition incorporating clinical, epidemiologic, and laboratory criteria. Of 1,460 unexplained respiratory illnesses reported by state and local health departments to the Centers for Disease Control and Prevention from March 17 to July 30, 2003, a total of 398 (27%) met clinical and epidemiologic SARS case criteria. Of these, 72 (18%) were probable cases with radiographic evidence of pneumonia. Eight (2%) were laboratory-confirmed SARS-coronavirus (SARS-CoV) infections, 206 (52%) were SARS-CoV negative, and 184 (46%) had undetermined SARS-CoV status because of missing convalescent-phase serum specimens. Thirty-one percent (124/398) of case-patients were hospitalized; none died. Travel was the most common epidemiologic link (329/398, 83%), and mainland China was the affected area most commonly visited. One case of possible household transmission was reported, and no laboratory-confirmed infections occurred among healthcare workers. Successes and limitations of this emergency surveillance can guide preparations for future outbreaks of SARS or respiratory diseases of unknown etiology

    Prokaryotic and Eukaryotic Community Structure in Field and Cultured Microbialites from the Alkaline Lake Alchichica (Mexico)

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    The geomicrobiology of crater lake microbialites remains largely unknown despite their evolutionary interest due to their resemblance to some Archaean analogs in the dominance of in situ carbonate precipitation over accretion. Here, we studied the diversity of archaea, bacteria and protists in microbialites of the alkaline Lake Alchichica from both field samples collected along a depth gradient (0–14 m depth) and long-term-maintained laboratory aquaria. Using small subunit (SSU) rRNA gene libraries and fingerprinting methods, we detected a wide diversity of bacteria and protists contrasting with a minor fraction of archaea. Oxygenic photosynthesizers were dominated by cyanobacteria, green algae and diatoms. Cyanobacterial diversity varied with depth, Oscillatoriales dominating shallow and intermediate microbialites and Pleurocapsales the deepest samples. The early-branching Gloeobacterales represented significant proportions in aquaria microbialites. Anoxygenic photosynthesizers were also diverse, comprising members of Alphaproteobacteria and Chloroflexi. Although photosynthetic microorganisms dominated in biomass, heterotrophic lineages were more diverse. We detected members of up to 21 bacterial phyla or candidate divisions, including lineages possibly involved in microbialite formation, such as sulfate-reducing Deltaproteobacteria but also Firmicutes and very diverse taxa likely able to degrade complex polymeric substances, such as Planctomycetales, Bacteroidetes and Verrucomicrobia. Heterotrophic eukaryotes were dominated by Fungi (including members of the basal Rozellida or Cryptomycota), Choanoflagellida, Nucleariida, Amoebozoa, Alveolata and Stramenopiles. The diversity and relative abundance of many eukaryotic lineages suggest an unforeseen role for protists in microbialite ecology. Many lineages from lake microbialites were successfully maintained in aquaria. Interestingly, the diversity detected in aquarium microbialites was higher than in field samples, possibly due to more stable and favorable laboratory conditions. The maintenance of highly diverse natural microbialites in laboratory aquaria holds promise to study the role of different metabolisms in the formation of these structures under controlled conditions
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