626 research outputs found

    A Snapshot Survey for Gravitational Lenses Among z>=4.0 Quasars: I. The z>5.7 Sample

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    Over the last few years, the Sloan Digital Sky Survey (SDSS) has discovered several hundred quasars with redshift between 4.0 and 6.4. Including the effects of magnification bias, one expects a priori that an appreciable fraction of these objects are gravitationally lensed. We have used the Advanced Camera for Surveys on the Hubble Space Telescope to carry out a snapshot imaging survey of high-redshift SDSS quasars to search for gravitationally split lenses. This paper, the first in a series reporting the results of the survey, describes snapshot observations of four quasars at z = 5.74, 5.82, 5.99 and 6.30, respectively. We find that none of these objects has a lensed companion within 5 magnitudes with a separation larger than 0.3 arcseconds; within 2.5 magnitudes, we can rule out companions within 0.1 arcseconds. Based on the non-detection of strong lensing in these four systems, we constrain the z~6 luminosity function to a slope of beta>-4.63 (3 sigma), assuming a break in the quasar luminosity function at M_{1450}^*=-24.0. We discuss the implications of this constraint on the ionizing background due to quasars in the early universe. Given that these quasars are not highly magnified, estimates of the masses of their central engines by the Eddington argument must be taken seriously, possibly challenging models of black hole formation.Comment: 23 pages, 8 figures, 2 tables, submitted to A

    Functional Enhancers at the Gene-Poor 8q24 Cancer-Linked Locus

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    Multiple discrete regions at 8q24 were recently shown to contain alleles that predispose to many cancers including prostate, breast, and colon. These regions are far from any annotated gene and their biological activities have been unknown. Here we profiled a 5-megabase chromatin segment encompassing all the risk regions for RNA expression, histone modifications, and locations occupied by RNA polymerase II and androgen receptor (AR). This led to the identification of several transcriptional enhancers, which were verified using reporter assays. Two enhancers in one risk region were occupied by AR and responded to androgen treatment; one contained a single nucleotide polymorphism (rs11986220) that resides within a FoxA1 binding site, with the prostate cancer risk allele facilitating both stronger FoxA1 binding and stronger androgen responsiveness. The study reported here exemplifies an approach that may be applied to any risk-associated allele in non-protein coding regions as it emerges from genome-wide association studies to better understand the genetic predisposition of complex diseases

    Quasar Clustering from SDSS DR5: Dependences on Physical Properties

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    Using a homogenous sample of 38,208 quasars with a sky coverage of 4000deg24000 {\rm deg^2} drawn from the SDSS Data Release Five quasar catalog, we study the dependence of quasar clustering on luminosity, virial black hole mass, quasar color, and radio loudness. At z<2.5z<2.5, quasar clustering depends weakly on luminosity and virial black hole mass, with typical uncertainty levels 10\sim 10% for the measured correlation lengths. These weak dependences are consistent with models in which substantial scatter between quasar luminosity, virial black hole mass and the host dark matter halo mass has diluted any clustering difference, where halo mass is assumed to be the relevant quantity that best correlates with clustering strength. However, the most luminous and most massive quasars are more strongly clustered (at the 2σ\sim 2\sigma level) than the remainder of the sample, which we attribute to the rapid increase of the bias factor at the high-mass end of host halos. We do not observe a strong dependence of clustering strength on quasar colors within our sample. On the other hand, radio-loud quasars are more strongly clustered than are radio-quiet quasars matched in redshift and optical luminosity (or virial black hole mass), consistent with local observations of radio galaxies and radio-loud type 2 AGN. Thus radio-loud quasars reside in more massive and denser environments in the biased halo clustering picture. Using the Sheth et al.(2001) formula for the linear halo bias, the estimated host halo mass for radio-loud quasars is 1013h1M\sim 10^{13} h^{-1}M_\odot, compared to 2×1012h1M\sim 2\times 10^{12} h^{-1}M_\odot for radio-quiet quasar hosts at z1.5z\sim 1.5.Comment: Updated version; accepted for publication in Ap

    The XMM Cluster Survey: Forecasting cosmological and cluster scaling-relation parameter constraints

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    We forecast the constraints on the values of sigma_8, Omega_m, and cluster scaling relation parameters which we expect to obtain from the XMM Cluster Survey (XCS). We assume a flat Lambda-CDM Universe and perform a Monte Carlo Markov Chain analysis of the evolution of the number density of galaxy clusters that takes into account a detailed simulated selection function. Comparing our current observed number of clusters shows good agreement with predictions. We determine the expected degradation of the constraints as a result of self-calibrating the luminosity-temperature relation (with scatter), including temperature measurement errors, and relying on photometric methods for the estimation of galaxy cluster redshifts. We examine the effects of systematic errors in scaling relation and measurement error assumptions. Using only (T,z) self-calibration, we expect to measure Omega_m to +-0.03 (and Omega_Lambda to the same accuracy assuming flatness), and sigma_8 to +-0.05, also constraining the normalization and slope of the luminosity-temperature relation to +-6 and +-13 per cent (at 1sigma) respectively in the process. Self-calibration fails to jointly constrain the scatter and redshift evolution of the luminosity-temperature relation significantly. Additional archival and/or follow-up data will improve on this. We do not expect measurement errors or imperfect knowledge of their distribution to degrade constraints significantly. Scaling-relation systematics can easily lead to cosmological constraints 2sigma or more away from the fiducial model. Our treatment is the first exact treatment to this level of detail, and introduces a new `smoothed ML' estimate of expected constraints.Comment: 28 pages, 17 figures. Revised version, as accepted for publication in MNRAS. High-resolution figures available at http://xcs-home.org (under "Publications"

    Comprehensive resequence analysis of a 136 kb region of human chromosome 8q24 associated with prostate and colon cancers

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    Recently, genome-wide association studies have identified loci across a segment of chromosome 8q24 (128,100,000–128,700,000) associated with the risk of breast, colon and prostate cancers. At least three regions of 8q24 have been independently associated with prostate cancer risk; the most centromeric of which appears to be population specific. Haplotypes in two contiguous but independent loci, marked by rs6983267 and rs1447295, have been identified in the Cancer Genetic Markers of Susceptibility project (http://cgems.cancer.gov), which genotyped more than 5,000 prostate cancer cases and 5,000 controls of European origin. The rs6983267 locus is also strongly associated with colorectal cancer. To ascertain a comprehensive catalog of common single-nucleotide polymorphisms (SNPs) across the two regions, we conducted a resequence analysis of 136 kb (chr8: 128,473,000–128,609,802) using the Roche/454 next-generation sequencing technology in 39 prostate cancer cases and 40 controls of European origin. We have characterized a comprehensive catalog of common (MAF > 1%) SNPs within this region, including 442 novel SNPs and have determined the pattern of linkage disequilibrium across the region. Our study has generated a detailed map of genetic variation across the region, which should be useful for choosing SNPs for fine mapping of association signals in 8q24 and investigations of the functional consequences of select common variants

    Ovarian cancer risk and common variation in the sex hormone-binding globulin gene: a population-based case-control study

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    BACKGROUND: The sex hormone-binding globulin (SHBG) is a carrier protein that modulates the bio-availability of serum sex steroid hormones, which may be involved in ovarian cancer. We evaluated whether common genetic variation in SHBG and its 3' neighbor ATP1B2, in linkage disequilibrium, is associated with the risk of epithelial ovarian cancer. METHODS: The study population included 264 women with ovarian carcinoma and 625 controls participating in a population-based case-control study in Poland. Five common single nucleotide polymorphisms (SNPs) in SHGB and five in ATP1B2 were selected to capture most common variation in this region. RESULTS: None of the SNPs evaluated was significantly associated with ovarian cancer risk, including the putative functional SNPs SHBG D356N (rs6259) and -67G>A 5'UTR (rs1799941). However, our data were consistent with a decreased ovarian cancer risk associated with the variant alleles for these two SNPs, which have been previously associated with increased circulating levels of SHBG. CONCLUSION: These data do not support a substantial association between common genetic variation in SHBG and ovarian cancer risk

    The Atacama Cosmology Telescope: Sunyaev Zel'dovich Selected Galaxy Clusters at 148 GHz in the 2008 Survey

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    We report on twenty-three clusters detected blindly as Sunyaev-Zel'dovich (SZ) decrements in a 148 GHz, 455 square-degree map of the southern sky made with data from the Atacama Cosmology Telescope 2008 observing season. All SZ detections announced in this work have confirmed optical counterparts. Ten of the clusters are new discoveries. One newly discovered cluster, ACT-CL J0102-4915, with a redshift of 0.75 (photometric), has an SZ decrement comparable to the most massive systems at lower redshifts. Simulations of the cluster recovery method reproduce the sample purity measured by optical follow-up. In particular, for clusters detected with a signal-to-noise ratio greater than six, simulations are consistent with optical follow-up that demonstrated this subsample is 100% pure. The simulations further imply that the total sample is 80% complete for clusters with mass in excess of 6x10^14 solar masses referenced to the cluster volume characterized by five hundred times the critical density. The Compton y -- X-ray luminosity mass comparison for the eleven best detected clusters visually agrees with both self-similar and non-adiabatic, simulation-derived scaling laws.Comment: 13 pages, 7 figures, Accepted for publication in Ap
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