45 research outputs found

    Galaxy Zoo : Building the low-mass end of the red sequence with local post-starburst galaxies

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    We present a study of local post-starburst galaxies (PSGs) using the photometric and spectroscopic observations from the Sloan Digital Sky Survey and the results from the Galaxy Zoo project. We find that the majority of our local PSG population have neither early- nor late-type morphologies but occupy a well-defined space within the colour-stellar mass diagram, most notably, the low-mass end of the 'green valley' below the transition mass thought to be the mass division between low-mass star-forming galaxies and high-mass passively evolving bulge-dominated galaxies. Our analysis suggests that it is likely that local PSGs will quickly transform into 'red', low-mass early-type galaxies as the stellar morphologies of the 'green' PSGs largely resemble that of the early-type galaxies within the same mass range. We propose that the current population of PSGs represents a population of galaxies which is rapidly transitioning between the star-forming and the passively evolving phases. Subsequently, these PSGs will contribute towards the build-up of the low-mass end of the 'red sequence' once the current population of young stars fade and stars are no longer being formed. These results are consistent with the idea of 'downsizing' where the build-up of smaller galaxies occurs at later epochs.Peer reviewe

    Galaxy Zoo Builder: Four-component Photometric Decomposition of Spiral Galaxies Guided by Citizen Science

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    Multicomponent modeling of galaxies is a valuable tool in the effort to quantitatively understand galaxy evolution, yet the use of the technique is plagued by issues of convergence, model selection, and parameter degeneracies. These issues limit its application over large samples to the simplest models, with complex models being applied only to very small samples. We attempt to resolve this dilemma of "quantity or quality"by developing a novel framework, built inside the Zooniverse citizen-science platform, to enable the crowdsourcing of model creation for Sloan Digital Sky Survey galaxies. We have applied the method, including a final algorithmic optimization step, on a test sample of 198 galaxies, and examine the robustness of this new method. We also compare it to automated fitting pipelines, demonstrating that it is possible to consistently recover accurate models that either show good agreement with, or improve on, prior work. We conclude that citizen science is a promising technique for modeling images of complex galaxies, and release our catalog of models

    Galaxy Zoo: Bulgeless galaxies with growing black holes

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    The growth of supermassive black holes appears to be driven by galaxy mergers, violent merger-free processes and/or 'secular' processes. In order to quantify the effects of secular evolution on black hole growth, we study a sample of active galactic nuclei (AGN) in galaxies with a calm formation history free of significant mergers, a population that heretofore has been difficult to locate. Here we present an initial sample of 13 AGN in massive (M ≳ 10M) bulgeless galaxies - which lack the classical bulges believed inevitably to result from mergers - selected from the Sloan Digital Sky Survey using visual classifications from Galaxy Zoo. Parametric morphological fitting confirms that the host galaxies lack classical bulges; any contributions from pseudo-bulges are very small (typicallyPeer reviewe

    Benchmarking Strain-Based Finite Element Model Validation

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    A nested case-control study of influenza vaccination was a cost-effective alternative to a full cohort analysis

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    OBJECTIVE: In the absence of trial results that are applicable to the target population, nested case-control studies might be an alternative to full-cohort analysis. We compared relative and absolute estimates of associations in an influenza vaccine study using both designs. STUDY DESIGN AND SETTING: Data from elderly persons enrolled during six consecutive influenza seasons were used (147,551 person-periods). The endpoints "hospitalization for pneumonia or influenza" (P&I) or "death" were used combined and separately to define three types of cases. Controls for the case-control samples were randomly selected from the remainder of the total cohort at different ratios (1:1 to 1:4). Logistic regression analysis was used to assess adjusted vaccine effectiveness (VE). Sampling fractions were used to determine the number needed to treat to prevent one outcome. Receiver-operator-curve analysis was conducted to estimate the area under the curve (AUC) as a measure of discriminative capacity of the prognostic model. RESULTS: In all, 978 P and I hospitalizations and 1,339 deaths were observed. The adjusted estimates of relative estimates (VE, AUC) and their corresponding 95% confidence intervals were virtually the same using both study designs, notably when the case-control ratio was high (1:4). CONCLUSION: A nested case-control design can provide valid and precise estimates of associations and is a cost-effective alternative for full-cohort analysis

    Do recommended high-risk adults benefit from a first influenza vaccination?

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    It is unknown whether a first influenza vaccination protects high-risk adults from severe morbidity and mortality during influenza epidemics. As part of the PRISMA nested case-control study, we aimed to evaluate the effectiveness of first-time and repeat influenza vaccinations in adult persons recommended for vaccination aged between 18 and 64 years during the 1999-2000 influenza A epidemic. After adjustments, 69% of hospitalizations for acute respiratory or cardiovascular disease or death were prevented in first-time vaccinees (95% percent confidence interval [95% CI]: 8-90%). The corresponding figure in persons who were vaccinated before was 85% (95% CI: 36-96%). Adult persons with high-risk medical conditions can substantially benefit from a first and repeat influenza vaccination prior to an epidemic. (c) 2006 Elsevier Ltd. All rights reserved

    Predicting Influenza Waves with Health Insurance Data

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    Antimicrobial and cytotoxic synergism of biocides and quorum-sensing inhibitors against uropathogenic Escherichia coli.

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    BackgroundUropathogenic Escherichia coli (UPEC) are a primary cause of catheter-associated urinary tract infections (CAUTIs), often forming mature recalcitrant biofilms on the catheter surface. Anti-infective catheter coatings containing single biocides have been developed but display limited antimicrobial activity due to the selection of biocide-resistant bacterial populations. Furthermore, biocides often display cytotoxicity at concentrations required to eradicate biofilms, limiting their antiseptic potential. Quorum-sensing inhibitors (QSIs) provide a novel anti-infective approach to disrupt biofilm formation on the catheter surface and help prevent CAUTIs.AimTo evaluate the combinatorial impact of biocides and QSIs at bacteriostatic, bactericidal and biofilm eradication concentrations in parallel to assessing cytotoxicity in a bladder smooth muscle (BSM) cell line.MethodsCheckerboard assays were performed to determine fractional inhibitory, bactericidal, and biofilm eradication concentrations of test combinations in UPEC and combined cytotoxic effects in BSM cells.FindingsSynergistic antimicrobial activity was observed between polyhexamethylene biguanide, benzalkonium chloride or silver nitrate in combination with either cinnamaldehyde or furanone-C30 against UPEC biofilms. However, furanone-C30 was cytotoxic at concentrations below those required for even bacteriostatic activity. A dose-dependent cytotoxicity profile was observed for cinnamaldehyde when in combination with BAC, PHMB or silver nitrate. Both PHMB and silver nitrate displayed combined bacteriostatic and bactericidal activity below the half-maximum inhibitory concentration (IC50). Triclosan in combination with both QSIs displayed antagonistic activity in both UPEC and BSM cells.ConclusionPHMB and silver in combination with cinnamaldehyde display synergistic antimicrobial activity in UPEC at non-cytotoxic concentrations, suggesting potential as anti-infective catheter-coating agents

    Clinical effectiveness of first and repeat influenza vaccination in adult and elderly diabetic patients

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    OBJECTIVE - influenza vaccine uptake remains low among the high-risk group of patients with diabetes, partly because of conflicting evidence regarding its potential benefits. We assessed the clinical effectiveness of influenza vaccination in adults with diabetes and specifically examined potential modification of effect by age and prior influenza vaccine uptake. RESEARCH DESIGN AND METHODS - The study was part of the Prevention of Influenza, Surveillance and Management (PRISMA) study, a nested case-control study conducted during the 1999-2000 influenza A epidemic, among 75,235 patients from primary care of any age recommended for vaccination. Among 9,238 adult patients with diabetes, 131 cases arose who were either hospitalized for diabetes dysregulation, acute respiratory disease, or cardiovascular disease and 61 cases who died, and we compared them with 1,561 control subjects. We evaluated the effect of (prior) influenza vaccination by means of logistic regression analysis controlling for age, sex, health insurance coverage, prior health care use, medication use, and comorbid conditions. RESULTS - Vaccination was associated with a 56% reduction in any complication (95% CI 36-70%), a 54% reduction in hospitalizations (26-71%), and 58% reduction in deaths (13-80%). Among study subjects aged 18-64 years, we observed somewhat higher reductions in the 0 occurrence of any complication than among those aged > 65 years (72 vs. 39%). in first-time vaccinated subjects, the primary end point was reduced by 47% (0.2-72%), and in those who received vaccination in the year before, the reduction was 58% (4-81%). CONCLUSIONS - Adults with type 2 diabetes, like other individuals from recognized risk groups, benefit considerably from influenza vaccination, and no difference in vaccine effectiveness was observed between first-time and repeat vaccination
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