14 research outputs found

    Properties of Type Ia supernovae inside rich galaxy clusters

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    We used the Gaussian Mixture Brightest Cluster Galaxy catalogue and Sloan Digital Sky Survey-II supernovae data with redshifts measured by the Baryon Oscillation Spectroscopic Survey to identify 48 Type Ia supernovae (SNe Ia) residing in rich galaxy clusters and compare their properties with 1015 SNe Ia in the field. Their light curves were parametrized by the SALT2 model and the significance of the observed differences was assessed by a resampling technique. To test our samples and methods, we first looked for known differences between SNe Ia residing in active and passive galaxies. We confirm that passive galaxies host SNe Ia with smaller stretch, weaker colour–luminosity relation [β of 2.54(22) against 3.35(14)], and that are ∼0.1 mag more luminous after stretch and colour corrections. We show that only 0.02 per cent of random samples drawn from our set of SNe Ia in active galaxies can reach these values. Reported differences in the Hubble residuals scatter could not be detected, possibly due to the exclusion of outliers. We then show that, while most field and cluster SNe Ia properties are compatible at the current level, their stretch distributions are different (∼3σ): besides having a higher concentration of passive galaxies than the field, the cluster’s passive galaxies host SNe Ia with an average stretch even smaller than those in field passive galaxies (at 95 per cent confidence).We argue that the older age of passive galaxies in clusters is responsible for this effect since, as we show, old passive galaxies host SNe Ia with smaller stretch than young passive galaxies (∼4σ).Web of Scienc

    Type II-P Supernovae from the SDSS-II Supernova Survey and the Standardized Candle Method

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    We apply the Standardized Candle Method (SCM) for Type II Plateau supernovae (SNe II-P), which relates the velocity of the ejecta of a SN to its luminosity during the plateau, to 15 SNe II-P discovered over the three season run of the Sloan Digital Sky Survey - II Supernova Survey. The redshifts of these SNe - 0.027 < z < 0.144 - cover a range hitherto sparsely sampled in the literature; in particular, our SNe II-P sample contains nearly as many SNe in the Hubble flow (z > 0.01) as all of the current literature on the SCM combined. We find that the SDSS SNe have a very small intrinsic I-band dispersion (0.22 mag), which can be attributed to selection effects. When the SCM is applied to the combined SDSS-plus-literature set of SNe II-P, the dispersion increases to 0.29 mag, larger than the scatter for either set of SNe separately. We show that the standardization cannot be further improved by eliminating SNe with positive plateau decline rates, as proposed in Poznanski et al. (2009). We thoroughly examine all potential systematic effects and conclude that for the SCM to be useful for cosmology, the methods currently used to determine the Fe II velocity at day 50 must be improved, and spectral templates able to encompass the intrinsic variations of Type II-P SNe will be needed.Comment: Accepted for publication by ApJ; data used in this paper can be downloaded from http://sdssdp47.fnal.gov/sdsssn/photometry/SNIIp.tgz; citation errors correcte

    Host galaxy identification for supernova surveys

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    Host galaxy identification is a crucial step for modern supernova (SN) surveys such as the Dark Energy Survey (DES) and the Large Synoptic Survey Telescope (LSST), which will discover SNe by the thousands. Spectroscopic resources are limited, so in the absence of real-time SN spectra these surveys must rely on host galaxy spectra to obtain accurate redshifts for the Hubble diagram and to improve photometric classification of SNe. In addition, SN luminosities are known to correlate with host-galaxy properties. Therefore, reliable identification of host galaxies is essential for cosmology and SN science. We simulate SN events and their locations within their host galaxies to develop and test methods for matching SNe to their hosts. We use both real and simulated galaxy catalog data from the Advanced Camera for Surveys General Catalog and MICECATv2.0, respectively. We also incorporate "hostless" SNe residing in undetected faint hosts into our analysis, with an assumed hostless rate of 5%. Our fully automated algorithm is run on catalog data and matches SNe to their hosts with 91% accuracy. We find that including a machine learning component, run after the initial matching algorithm, improves the accuracy (purity) of the matching to 97% with a 2% cost in efficiency (true positive rate). Although the exact results are dependent on the details of the survey and the galaxy catalogs used, the method of identifying host galaxies we outline here can be applied to any transient survey

    Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants with Treatment Resistance in Schizophrenia

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    Importance: About 20% to 30% of people with schizophrenia have psychotic symptoms that do not respond adequately to first-line antipsychotic treatment. This clinical presentation, chronic and highly disabling, is known as treatment-resistant schizophrenia (TRS). The causes of treatment resistance and their relationships with causes underlying schizophrenia are largely unknown. Adequately powered genetic studies of TRS are scarce because of the difficulty in collecting data from well-characterized TRS cohorts. Objective: To examine the genetic architecture of TRS through the reassessment of genetic data from schizophrenia studies and its validation in carefully ascertained clinical samples. Design, Setting, and Participants: Two case-control genome-wide association studies (GWASs) of schizophrenia were performed in which the case samples were defined as individuals with TRS (n = 10501) and individuals with non-TRS (n = 20325). The differences in effect sizes for allelic associations were then determined between both studies, the reasoning being such differences reflect treatment resistance instead of schizophrenia. Genotype data were retrieved from the CLOZUK and Psychiatric Genomics Consortium (PGC) schizophrenia studies. The output was validated using polygenic risk score (PRS) profiling of 2 independent schizophrenia cohorts with TRS and non-TRS: a prevalence sample with 817 individuals (Cardiff Cognition in Schizophrenia [CardiffCOGS]) and an incidence sample with 563 individuals (Genetics Workstream of the Schizophrenia Treatment Resistance and Therapeutic Advances [STRATA-G]). Main Outcomes and Measures: GWAS of treatment resistance in schizophrenia. The results of the GWAS were compared with complex polygenic traits through a genetic correlation approach and were used for PRS analysis on the independent validation cohorts using the same TRS definition. Results: The study included a total of 85490 participants (48635 [56.9%] male) in its GWAS stage and 1380 participants (859 [62.2%] male) in its PRS validation stage. Treatment resistance in schizophrenia emerged as a polygenic trait with detectable heritability (1% to 4%), and several traits related to intelligence and cognition were found to be genetically correlated with it (genetic correlation, 0.41-0.69). PRS analysis in the CardiffCOGS prevalence sample showed a positive association between TRS and a history of taking clozapine (r2 = 2.03%; P =.001), which was replicated in the STRATA-G incidence sample (r2 = 1.09%; P =.04). Conclusions and Relevance: In this GWAS, common genetic variants were differentially associated with TRS, and these associations may have been obscured through the amalgamation of large GWAS samples in previous studies of broadly defined schizophrenia. Findings of this study suggest the validity of meta-analytic approaches for studies on patient outcomes, including treatment resistance

    First cosmology results using Type Ia supernova from the Dark Energy Survey: simulations to correct supernova distance biases

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    We describe catalogue-level simulations of Type Ia supernova (SN Ia) light curves in the Dark Energy Survey Supernova Program (DES-SN) and in low-redshift samples from the Center for Astrophysics (CfA) and the Carnegie Supernova Project (CSP). These simulations are used to model biases from selection effects and light-curve analysis and to determine bias corrections for SN Ia distance moduli that are used to measure cosmological parameters. To generate realistic light curves, the simulation uses a detailed SN Ia model, incorporates information from observations (point spread function, sky noise, zero-point), and uses summary information (e.g. detection efficiency versus signal-to-noise ratio) based on 10 000 fake SN light curves whose fluxes were overlaid on images and processed with our analysis pipelines. The quality of the simulation is illustrated by predicting distributions observed in the data. Averaging within redshift bins, we find distance modulus biases up to 0.05 mag over the redshift ranges of the low-z and DES-SN samples. For individual events, particularly those with extreme red or blue colour, distance biases can reach 0.4 mag. Therefore, accurately determining bias corrections is critical for precision measurements of cosmological parameters.ISSN:0035-8711ISSN:1365-296
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