University of Arizona

About: University of Arizona is a education organization based out in Tucson, Arizona, United States. It is known for research contribution in the topics: Population & Galaxy. The organization has 63805 authors who have published 155998 publications receiving 6854915 citations. The organization is also known as: UA & U of A.

The 16th Data Release of the Sloan Digital Sky Surveys: First Release from the APOGEE-2 Southern Survey and Full Release of eBOSS Spectra

Abstract: This paper documents the sixteenth data release (DR16) from the Sloan Digital Sky Surveys; the fourth and penultimate from the fourth phase (SDSS-IV). This is the first release of data from the southern hemisphere survey of the Apache Point Observatory Galactic Evolution Experiment 2 (APOGEE-2); new data from APOGEE-2 North are also included. DR16 is also notable as the final data release for the main cosmological program of the Extended Baryon Oscillation Spectroscopic Survey (eBOSS), and all raw and reduced spectra from that project are released here. DR16 also includes all the data from the Time Domain Spectroscopic Survey (TDSS) and new data from the SPectroscopic IDentification of ERosita Survey (SPIDERS) programs, both of which were co-observed on eBOSS plates. DR16 has no new data from the Mapping Nearby Galaxies at Apache Point Observatory (MaNGA) survey (or the MaNGA Stellar Library "MaStar"). We also preview future SDSS-V operations (due to start in 2020), and summarize plans for the final SDSS-IV data release (DR17).

Nearby Supernova Rates from the Lick Observatory Supernova Search. II. The Observed Luminosity Functions and Fractions of Supernovae in a Complete Sample

Abstract: This is the second paper of a series in which we present new measurements of the observed rates of supernovae (SNe) in the local Universe, determined from the Lick Observatory Supernova Search (LOSS). In this paper, a complete SN sample is constructed, and the observed (uncorrected for host-galaxy extinction) luminosity functions (LFs) of SNe are derived. These LFs solve two issues that have plagued previous rate calculations for nearby SNe: the luminosity distribution of SNe and the host-galaxy extinction. We select a volume-limited sample of 175 SNe, collect photometry for every object, and fit a family of light curves to constrain the peak magnitudes and light-curve shapes. The volume-limited LFs show that they are not well represented by a Gaussian distribution. There are notable differences in the LFs for galaxies of different Hubble types (especially for SNe Ia). We derive the observed fractions for the different subclasses in a complete SN sample, and find significant fractions of SNe II-L (10%), IIb (12%), and IIn (9%) in the SN II sample. Furthermore, we derive the LFs and the observed fractions of different SN subclasses in a magnitudelimited survey with different observation intervals, and find that the LFs are enhanced at the high-luminosity end and appear more “standard” with smaller scatter, and that the LFs and fractions of SNe do not change significantly when the observation interval is shorter than 10 d. We also discuss the LFs in different galaxy sizes and inclinations, and for different SN subclasses. Some notable results are that there is not a strong correlation between the SN LFs and the host-galaxy size, but there might be a preference for SNe IIn to occur in small, late-type spiral galaxies. The LFs in different inclination bins do not provide strong evidence for extreme extinction in highly inclined galaxies, though the sample is still small. The LFs of different SN subclasses show significant differences. We also find that SNe Ibc and IIb come from more luminous galaxies than SNe II-P, while SNe IIn come from less luminous galaxies, suggesting a possible metallicity effect. The limitations and applications of our LFs are also discussed.

Watermarking, tamper-proofing, and obfuscation - tools for software protection

Abstract: We identify three types of attack on the intellectual property contained in software and three corresponding technical defenses. A defense against reverse engineering is obfuscation, a process that renders software unintelligible but still functional. A defense against software piracy is watermarking, a process that makes it possible to determine the origin of software. A defense against tampering is tamper-proofing, so that unauthorized modifications to software (for example, to remove a watermark) will result in nonfunctional code. We briefly survey the available technology for each type of defense.

The shared landscape: what does aesthetics have to do with ecology?

Abstract: This collaborative essay grows out of a debate about the relationship between aesthetics and ecology and the possibility of an “ecological aesthetic” that affects landscape planning, design, and management. We describe our common understandings and unresolved questions about this relationship, including the importance of aesthetics in understanding and affecting landscape change and the ways in which aesthetics and ecology may have either complementary or contradictory implications for a landscape. To help understand these issues, we first outline a conceptual model of the aesthetics–ecology relationship. We posit that: 1. While human and environmental phenomena occur at widely varying scales, humans engage with environmental phenomena at a particular scale: that of human experience of our landscape surroundings. That is the human “perceptible realm.” 2. Interactions within this realm give rise to aesthetic experiences, which can lead to changes affecting humans and the landscape, and thus ecosystems. 3. Context affects aesthetic experience of landscapes. Context includes both effects of different landscape types (wild, agricultural, cultural, and metropolitan landscapes) and effects of different personal–social situational activities or concerns. We argue that some contexts elicit aesthetic experiences that have traditionally been called “scenic beauty,” while other contexts elicit different aesthetic experiences, such as perceived care, attachment, and identity. Last, we discuss how interventions through landscape planning, design, and management; or through enhanced knowledge might establish desirable relationships between aesthetics and ecology, and we examine the controversial characteristics of such ecological aesthetics. While these interventions may help sustain beneficial landscape patterns and practices, they are inherently normative, and we consider their ethical implications.

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program.

Abstract: The Trans-Omics for Precision Medicine (TOPMed) programme seeks to elucidate the genetic architecture and biology of heart, lung, blood and sleep disorders, with the ultimate goal of improving diagnosis, treatment and prevention of these diseases The initial phases of the programme focused on whole-genome sequencing of individuals with rich phenotypic data and diverse backgrounds Here we describe the TOPMed goals and design as well as the available resources and early insights obtained from the sequence data The resources include a variant browser, a genotype imputation server, and genomic and phenotypic data that are available through dbGaP (Database of Genotypes and Phenotypes)1 In the first 53,831 TOPMed samples, we detected more than 400 million single-nucleotide and insertion or deletion variants after alignment with the reference genome Additional previously undescribed variants were detected through assembly of unmapped reads and customized analysis in highly variable loci Among the more than 400 million detected variants, 97% have frequencies of less than 1% and 46% are singletons that are present in only one individual (53% among unrelated individuals) These rare variants provide insights into mutational processes and recent human evolutionary history The extensive catalogue of genetic variation in TOPMed studies provides unique opportunities for exploring the contributions of rare and noncoding sequence variants to phenotypic variation Furthermore, combining TOPMed haplotypes with modern imputation methods improves the power and reach of genome-wide association studies to include variants down to a frequency of approximately 001% The goals, resources and design of the NHLBI Trans-Omics for Precision Medicine (TOPMed) programme are described, and analyses of rare variants detected in the first 53,831 samples provide insights into mutational processes and recent human evolutionary history