52 research outputs found

    Documenting Disasters: A Focus on Floods

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    A more thorough understanding of disasters can help archivists assemble and acquire collections of depth that will be of wide use to scholars, survivors, and others. To investigate the broader context of disasters, the focus of this article is on natural disasters, looking at floods in particular, with the hope that the information can be applied to other tragedies. The article includes an in-depth examination of disaster studies literature of assistance to archivists, along with accounts of experiences working with flood collections

    Tracing the Source of Irrigation: An Examination of Colorado Ditch Company Collections in Archival Repositories

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    The history of irrigation is significant in the western United States, which has now experienced over 150 years of irrigation development. When considered fully, the history of Western irrigation goes beyond agriculture and extends to engineering, economics, business, sociology, law, politics, ecology, and more. The historical understanding to be gained from any of these viewpoints depends on the preservation and accessibility of original records created by irrigators. In the West, ditch company records are the earliest and best source of irrigation history. This article examines to what extent historical records of Colorado ditch companies have been preserved in and made accessible through public archival repositories. It also contextualizes ditch companies and their records and makes recommendations so such records can be available for a variety of research

    "The beginning of everything": a five-year report on the Colorado State University Water Resources Archive

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    Includes bibliographical references (pages 13-17)

    Colorado water history: a bibliography

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    March 2008.Water is at the heart of Colorado's past and future. Ongoing debates - even lawsuits - regarding water show the importance this vital resource to the state and to the West. Combined with natural disasters such as floods and drought, or human concerns such as pollution and recreation, water issues have drawn an increasing degree of public attention. For water professionals, students, and interested citizens, knowing the history of our water resources can lead to a better understanding of current issues and events. The Colorado Water History Bibliography is a helpful resource for those wanting to learn more about this timely and significant topic. This bibliography is not intended to be comprehensive. Rather, it is a selective listing of core books on the topic that are generally accessible to the public, both in terms of content and availability. In addition to illuminating books already written about Colorado's water, this list reveals areas ripe for research. There are clearly holes in the writings about our state's rich water history, waiting to be filled in by generations of scholars yet to come

    Developing a metadata best practices model: the experience of the Colorado State University Libraries

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    Final, peer-reviewed manuscript.The Metadata Best Practices Task Force at the Colorado State University (CSU) Libraries developed a core set of metadata elements and an accompanying data dictionary to facilitate a coordinated metadata management approach for a central digital repository of diverse digital objects. This article describes the rationale for the Task Force and the process used for its work following a look at the background of digitization and past metadata practices at CSU. The article includes a literature review on institutional metadata projects and examples, and it ends with a description of the Task Force's ongoing work and plans for future assessment

    Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney.

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    Elevated blood pressure is a major risk factor for cardiovascular disease and has a substantial genetic contribution. Genetic variation influencing blood pressure has the potential to identify new pharmacological targets for the treatment of hypertension. To discover additional novel blood pressure loci, we used 1000 Genomes Project-based imputation in 150 134 European ancestry individuals and sought significant evidence for independent replication in a further 228 245 individuals. We report 6 new signals of association in or near HSPB7, TNXB, LRP12, LOC283335, SEPT9, and AKT2, and provide new replication evidence for a further 2 signals in EBF2 and NFKBIA Combining large whole-blood gene expression resources totaling 12 607 individuals, we investigated all novel and previously reported signals and identified 48 genes with evidence for involvement in blood pressure regulation that are significant in multiple resources. Three novel kidney-specific signals were also detected. These robustly implicated genes may provide new leads for therapeutic innovation

    Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.

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    Numerous genetic loci have been associated with systolic blood pressure (SBP) and diastolic blood pressure (DBP) in Europeans. We now report genome-wide association studies of pulse pressure (PP) and mean arterial pressure (MAP). In discovery (N = 74,064) and follow-up studies (N = 48,607), we identified at genome-wide significance (P = 2.7 × 10(-8) to P = 2.3 × 10(-13)) four new PP loci (at 4q12 near CHIC2, 7q22.3 near PIK3CG, 8q24.12 in NOV and 11q24.3 near ADAMTS8), two new MAP loci (3p21.31 in MAP4 and 10q25.3 near ADRB1) and one locus associated with both of these traits (2q24.3 near FIGN) that has also recently been associated with SBP in east Asians. For three of the new PP loci, the estimated effect for SBP was opposite of that for DBP, in contrast to the majority of common SBP- and DBP-associated variants, which show concordant effects on both traits. These findings suggest new genetic pathways underlying blood pressure variation, some of which may differentially influence SBP and DBP

    Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.

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    Blood pressure is a heritable trait influenced by several biological pathways and responsive to environmental stimuli. Over one billion people worldwide have hypertension (≥140 mm Hg systolic blood pressure or  ≥90 mm Hg diastolic blood pressure). Even small increments in blood pressure are associated with an increased risk of cardiovascular events. This genome-wide association study of systolic and diastolic blood pressure, which used a multi-stage design in 200,000 individuals of European descent, identified sixteen novel loci: six of these loci contain genes previously known or suspected to regulate blood pressure (GUCY1A3-GUCY1B3, NPR3-C5orf23, ADM, FURIN-FES, GOSR2, GNAS-EDN3); the other ten provide new clues to blood pressure physiology. A genetic risk score based on 29 genome-wide significant variants was associated with hypertension, left ventricular wall thickness, stroke and coronary artery disease, but not kidney disease or kidney function. We also observed associations with blood pressure in East Asian, South Asian and African ancestry individuals. Our findings provide new insights into the genetics and biology of blood pressure, and suggest potential novel therapeutic pathways for cardiovascular disease prevention

    Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study

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    The prevalence of hypertension in African Americans (AAs) is higher than in other US groups; yet, few have performed genome-wide association studies (GWASs) in AA. Among people of European descent, GWASs have identified genetic variants at 13 loci that are associated with blood pressure. It is unknown if these variants confer susceptibility in people of African ancestry. Here, we examined genome-wide and candidate gene associations with systolic blood pressure (SBP) and diastolic blood pressure (DBP) using the Candidate Gene Association Resource (CARe) consortium consisting of 8591 AAs. Genotypes included genome-wide single-nucleotide polymorphism (SNP) data utilizing the Affymetrix 6.0 array with imputation to 2.5 million HapMap SNPs and candidate gene SNP data utilizing a 50K cardiovascular gene-centric array (ITMAT-Broad-CARe [IBC] array). For Affymetrix data, the strongest signal for DBP was rs10474346 (P= 3.6 × 10−8) located near GPR98 and ARRDC3. For SBP, the strongest signal was rs2258119 in C21orf91 (P= 4.7 × 10−8). The top IBC association for SBP was rs2012318 (P= 6.4 × 10−6) near SLC25A42 and for DBP was rs2523586 (P= 1.3 × 10−6) near HLA-B. None of the top variants replicated in additional AA (n = 11 882) or European-American (n = 69 899) cohorts. We replicated previously reported European-American blood pressure SNPs in our AA samples (SH2B3, P= 0.009; TBX3-TBX5, P= 0.03; and CSK-ULK3, P= 0.0004). These genetic loci represent the best evidence of genetic influences on SBP and DBP in AAs to date. More broadly, this work supports that notion that blood pressure among AAs is a trait with genetic underpinnings but also with significant complexit

    The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

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    To dissect the genetic architecture of blood pressure and assess effects on target-organ damage, we analyzed 128,272 SNPs from targeted and genome-wide arrays in 201,529 individuals of European ancestry and genotypes from an additional 140,886 individuals were used for validation. We identified 66 blood pressure loci, of which 17 were novel and 15 harbored multiple distinct association signals. The 66 index SNPs were enriched for cis-regulatory elements, particularly in vascular endothelial cells, consistent with a primary role in blood pressure control through modulation of vascular tone across multiple tissues. The 66 index SNPs combined in a risk score showed comparable effects in 64,421 individuals of non-European descent. The 66-SNP blood pressure risk score was significantly associated with target-organ damage in multiple tissues, with minor effects in the kidney. Our findings expand current knowledge of blood pressure pathways and highlight tissues beyond the classic renal system in blood pressure regulation
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