Observational Evidence from Supernovae for an Accelerating Universe and a Cosmological Constant

We present observations of 10 type Ia supernovae (SNe Ia) between 0.16 < z < 0.62. With previous data from our High-Z Supernova Search Team, this expanded set of 16 high-redshift supernovae and 34 nearby supernovae are used to place constraints on the Hubble constant (H_0), the mass density (Omega_M), the cosmological constant (Omega_Lambda), the deceleration parameter (q_0), and the dynamical age of the Universe (t_0). The distances of the high-redshift SNe Ia are, on average, 10% to 15% farther than expected in a low mass density (Omega_M=0.2) Universe without a cosmological constant. Different light curve fitting methods, SN Ia subsamples, and prior constraints unanimously favor eternally expanding models with positive cosmological constant (i.e., Omega_Lambda > 0) and a current acceleration of the expansion (i.e., q_0 < 0). With no prior constraint on mass density other than Omega_M > 0, the spectroscopically confirmed SNe Ia are consistent with q_0 <0 at the 2.8 sigma and 3.9 sigma confidence levels, and with Omega_Lambda >0 at the 3.0 sigma and 4.0 sigma confidence levels, for two fitting methods respectively. Fixing a ``minimal'' mass density, Omega_M=0.2, results in the weakest detection, Omega_Lambda>0 at the 3.0 sigma confidence level. For a flat-Universe prior (Omega_M+Omega_Lambda=1), the spectroscopically confirmed SNe Ia require Omega_Lambda >0 at 7 sigma and 9 sigma level for the two fitting methods. A Universe closed by ordinary matter (i.e., Omega_M=1) is ruled out at the 7 sigma to 8 sigma level. We estimate the size of systematic errors, including evolution, extinction, sample selection bias, local flows, gravitational lensing, and sample contamination. Presently, none of these effects reconciles the data with Omega_Lambda=0 and q_0 > 0.Comment: 36 pages, 13 figures, 3 table files Accepted to the Astronomical Journa

Supernova Limits on the Cosmic Equation of State

We use Type Ia supernovae studied by the High-Z Supernova Search Team to constrain the properties of an energy component which may have contributed to accelerating the cosmic expansion. We find that for a flat geometry the equation of state parameter for the unknown component, alpha_x=P_x/rho_x, must be less than -0.55 (95% confidence) for any value of Omega_m and is further limited to alpha_x<-0.60 (95%) if Omega_m is assumed to be greater than 0.1 . These values are inconsistent with the unknown component being topological defects such as domain walls, strings, or textures. The supernova data are consistent with a cosmological constant (alpha_x=-1) or a scalar field which has had, on average, an equation of state parameter similar to the cosmological constant value of -1 over the redshift range of z=1 to the present. Supernova and cosmic microwave background observations give complementary constraints on the densities of matter and the unknown component. If only matter and vacuum energy are considered, then the current combined data sets provide direct evidence for a spatially flat Universe with Omega_tot=Omega_m+Omega_Lambda = 0.94 +/- 0.26 (1-sigma).Comment: Accepted for publication in ApJ, 3 figure

Hubble Space Telescope and Ground-Based Observations of Type Ia Supernovae at Redshift 0.5: Cosmological Implications

We present observations of the Type Ia supernovae (SNe) 1999M, 1999N, 1999Q, 1999S, and 1999U, at redshift z~0.5. They were discovered in early 1999 with the 4.0~m Blanco telescope at Cerro Tololo Inter-American Observatory by the High-z Supernova Search Team (HZT) and subsequently followed with many ground-based telescopes. SNe 1999Q and 1999U were also observed with the Hubble Space Telescope. We computed luminosity distances to the new SNe using two methods, and added them to the high-z Hubble diagram that the HZT has been constructing since 1995. The new distance moduli confirm the results of previous work. At z~0.5, luminosity distances are larger than those expected for an empty universe, implying that a ``Cosmological Constant,'' or another form of ``dark energy,'' has been increasing the expansion rate of the Universe during the last few billion years.Comment: 68 pages, 22 figures. Scheduled for the 01 February 2006 issue of Ap.J. (v637

The STIS Parallel Survey: Introduction and First Results

The installation of the Space Telescope Imaging Spectrograph (STIS) on the Hubble Space Telescope (HST) allows for the first time two-dimensional optical and ultraviolet slitless spectroscopy of faint objects from space. The STIS Parallel Survey (SPS) routinely obtains broad band images and slitless spectra of random fields in parallel with HST observations using other instruments. The SPS is designed to study a wide variety of astrophysical phenomena, including the rate of star formation in galaxies at intermediate to high redshift through the detection of emission-line galaxies. We present the first results of the SPS, which demonstrate the capability of STIS slitless spectroscopy to detect and identify high-redshift galaxies.Comment: 11 pages, Latex, 3 enclosed Postscript figures, aaspp4.sty, accepted for publication in the Astrophysical Journal Letters HST Second Servicing Mission special issu

Meta-analysis of genome-wide association studies of asthma in ethnically diverse North American populations.

Asthma is a common disease with a complex risk architecture including both genetic and environmental factors. We performed a meta-analysis of North American genome-wide association studies of asthma in 5,416 individuals with asthma (cases) including individuals of European American, African American or African Caribbean, and Latino ancestry, with replication in an additional 12,649 individuals from the same ethnic groups. We identified five susceptibility loci. Four were at previously reported loci on 17q21, near IL1RL1, TSLP and IL33, but we report for the first time, to our knowledge, that these loci are associated with asthma risk in three ethnic groups. In addition, we identified a new asthma susceptibility locus at PYHIN1, with the association being specific to individuals of African descent (P = 3.9 × 10(-9)). These results suggest that some asthma susceptibility loci are robust to differences in ancestry when sufficiently large samples sizes are investigated, and that ancestry-specific associations also contribute to the complex genetic architecture of asthma

The High-Z Supernova Search: Measuring Cosmic Deceleration and Global Curvature of the Universe Using Type IA Supernovae

The High-Z Supernova Search is an international collaboration to discover and monitor Type Ia supernovae (SNe Ia) at z > 0.2 with the aim of measuring cosmic deceleration and global curvature. Our collaboration has pursued a basic understanding of supernovae in the nearby universe, discovering and observing a large sample of objects and developing methods to measure accurate distances with SNe Ia. This paper describes the extension of this program to z >= 0.2, outlining our search techniques and follow-up program. We have devised high-throughput filters that provide accurate two-color rest frame B and V light curves of SNe Ia, enabling us to produce precise, extinction-corrected luminosity distances in the range 0.25 < z < 0.55. Sources of systematic error from K-corrections, extinction, selection effects, and evolution are investigated, and their effects estimated. We present photometric and spectral observations of SN 1995K, our program's first supernova (SN), and use the data to obtain a precise measurement of the luminosity distance to the z = 0.479 host galaxy. This object, when combined with a nearby sample of SNe, yields an estimate for the matter density of the universe of ΩM=-0.2+1.0-0.8 if ΩΛ = 0. For a spatially flat universe composed of normal matter and a cosmological constant, we find ΩM=0.4+0.5-0.4, ΩΛ=0.6+0.4-0.5. We demonstrate that with a sample of ~30 objects, we should be able to determine relative luminosity distances over the range 0 < z < 0.5 with sufficient precision to measure ΩM with an uncertainty of +/-0.2.We wish to thank Ed Carter at NOAO for tracing the redshifted Ðlter set. A. V. F. acknowledges support from NSF grant AST 94-17213. R. P. K. acknowledges support from NSF grants AST 95-28899 and AST 96 17058 and thanks the Institute for Theoretical Physics, University of California, Santa Barbara, for their generous hospitality. A. G. R. acknowledges support from the Miller Institute for Basic Research in Science, University of California, Berkeley. SN research at UW is supported by the NSF and NASA. C. W. S. acknowledges the generous support of the Seaver Institute and the Packard Foundation. M. H. acknowledges support provided for this work by the NSF through grant number GF-1002-97 from the Association of Universities for Research in Astronomy, Inc., under NSF Cooperative Agreement No. AST 89-47990, and from Fundacio n Andes under project C-12984; M. H. also acknowledges support by Ca tedra Presidencial de Ciencias 1996-1997. Partial support for A. C. was provided by the NSF through grant GF-1001-95 from AURA, Inc., under NSF cooperative agreement AST 89-47990, and from Fundacio n Antorchas Argentina under project A-13313. This research used IRAF, an astronomical reduction package distributed by the National Optical Astronomy Observatories, which is operated by the Association of Universities for Research in Astronomy, Inc. (AURA), under cooperative agreement with the NSF

The Apache Point Observatory Galactic Evolution Experiment (APOGEE)

The Apache Point Observatory Galactic Evolution Experiment (APOGEE), one of the programs in the Sloan Digital Sky Survey III (SDSS-III), has now completed its systematic, homogeneous spectroscopic survey sampling all major populations of the Milky Way. After a three-year observing campaign on the Sloan 2.5 m Telescope, APOGEE has collected a half million high-resolution (R ~ 22,500), high signal-to-noise ratio (>100), infrared (1.51–1.70 μm) spectra for 146,000 stars, with time series information via repeat visits to most of these stars. This paper describes the motivations for the survey and its overall design—hardware, field placement, target selection, operations—and gives an overview of these aspects as well as the data reduction, analysis, and products. An index is also given to the complement of technical papers that describe various critical survey components in detail. Finally, we discuss the achieved survey performance and illustrate the variety of potential uses of the data products by way of a number of science demonstrations, which span from time series analysis of stellar spectral variations and radial velocity variations from stellar companions, to spatial maps of kinematics, metallicity, and abundance patterns across the Galaxy and as a function of age, to new views of the interstellar medium, the chemistry of star clusters, and the discovery of rare stellar species. As part of SDSS-III Data Release 12 and later releases, all of the APOGEE data products are publicly available

Ethnic-specific associations of rare and low-frequency DNA sequence variants with asthma

Common variants at many loci have been robustly associated with asthma but explain little of the overall genetic risk. Here we investigate the role of rare (<1%) and low-frequency (1–5%) variants using the Illumina HumanExome BeadChip array in 4,794 asthma cases, 4,707 non-asthmatic controls and 590 case–parent trios representing European Americans, African Americans/African Caribbeans and Latinos. Our study reveals one low-frequency missense mutation in the GRASP gene that is associated with asthma in the Latino sample (P=4.31 × 10−6; OR=1.25; MAF=1.21%) and two genes harbouring functional variants that are associated with asthma in a gene-based analysis: GSDMB at the 17q12–21 asthma locus in the Latino and combined samples (P=7.81 × 10−8 and 4.09 × 10−8, respectively) and MTHFR in the African ancestry sample (P=1.72 × 10−6). Our results suggest that associations with rare and low-frequency variants are ethnic specific and not likely to explain a significant proportion of the ‘missing heritability’ of asthma

The genetic determinants of recurrent somatic mutations in 43,693 blood genomes

Nononcogenic somatic mutations are thought to be uncommon and inconsequential. To test this, we analyzed 43,693 National Heart, Lung and Blood Institute Trans-Omics for Precision Medicine blood whole genomes from 37 cohorts and identified 7131 non-missense somatic mutations that are recurrently mutated in at least 50 individuals. These recurrent non-missense somatic mutations (RNMSMs) are not clearly explained by other clonal phenomena such as clonal hematopoiesis. RNMSM prevalence increased with age, with an average 50-year-old having 27 RNMSMs. Inherited germline variation associated with RNMSM acquisition. These variants were found in genes involved in adaptive immune function, proinflammatory cytokine production, and lymphoid lineage commitment. In addition, the presence of eight specific RNMSMs associated with blood cell traits at effect sizes comparable to Mendelian genetic mutations. Overall, we found that somatic mutations in blood are an unexpectedly common phenomenon with ancestry-specific determinants and human health consequences