713 research outputs found
STR-855: INSTANTANEOUS DEFLECTIONS OF CONCRETE SLABS COMPUTED USING DISCRETIZED ANALYSIS
Excessive deflection of concrete floor slabs is a recurring serviceability problem (Gilbert 2012, Stivaros 2012). Current practice is to compute deflections using either a single-element idealization, where an average effective moment of inertia is assigned to the entire member, or a discretized analysis, where the member is idealized as discrete elements with unique effective moments of inertia. There are two equations available for calculating the effective moment of inertia, developed by Branson (1965) and by Bischoff (2005). Branson originally proposed two equations for effective moment of inertia, a 3rd-power equation for use in a single-element idealization and a 4th-power equation for use in a discretized-element idealization. Bischoff has proposed a single equation, based on a correct mechanical model, for use in a single-element idealization only. The research summarized in this paper investigates suitable modifications to Bischoff’s Equation for use in a discretized analysis. Simply supported members with various reinforcement ratios and live- to dead-load ratios are explored. Comparisons to experimental data are made to determine which deflection calculation procedure provides results closest to those observed
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Vegetation Description, Rare Plant Inventory, and Vegetation Monitoring for Craig Mountain, Idaho.
The Craig Mountain Wildlife Mitigation Area was purchased by Bonneville Power Administration (BPA) as partial mitigation for wildlife losses incurred with the inundation of Dworshak Reservoir on the North Fork Clearwater River. Upon completion of the National Environmental Protection Act (NEPA) process, it is proposed that title to mitigation lands will be given to the Idaho Department of Fish and Game (IDFG). Craig Mountain is located at the northern end of the Hells Canyon Ecosystem. It encompasses the plateau and steep canyon slopes extending from the confluence of the Snake and Salmon rivers, northward to near Waha, south of Lewiston, Idaho. The forested summit of Craig Mountain is characterized by gently rolling terrain. The highlands dramatically break into the canyons of the Snake and Salmon rivers at approximately the 4,700 foot contour. The highly dissected canyons are dominated by grassland slopes containing a mosaic of shrubfield, riparian, and woodland habitats. During the 1993 and 1994 field seasons, wildlife, habitat/vegetation, timber, and other resources were systematically inventoried at Craig Mountain to provide Fish and Game managers with information needed to draft an ecologically-based management plan. The results of the habitat/vegetation portion of the inventory are contained in this report. The responsibilities for the Craig Mountain project included: (1) vegetation data collection, and vegetation classification, to help produce a GIS-generated Craig Mountain vegetation map, (2) to determine the distribution and abundance of rare plants populations and make recommendations concerning their management, and (3) to establish a vegetation monitoring program to evaluate the effects of Fish and Game management actions, and to assess progress towards meeting habitat mitigation goals
Noncommutative partially convex rational functions
Motivated by classical notions of bilinear matrix inequalities (BMIs) and
partial convexity, this article investigates partial convexity for
noncommutative functions. It is shown that noncommutative rational functions
that are partially convex admit novel butterfly-type realizations that
necessitate square roots. The notion of xy-convexity, a strengthening of
partial convexity arising in connection with BMIs, is also considered. A
characterization of xy-convex polynomials is given
Deliverable D4.4 Simulated coherent scattering data from plasma and non–plasma samples
Deliverable D4.4 of work package 4 (SIMEX) in EUCALL
Factor VIII: Long-established role in haemophilia A and emerging evidence beyond haemostasis
Abstract Factor VIII protein (FVIII) as a coagulation replacement factor has for decades been used as the standard of care for management of people with haemophilia A. It is effective for treatment of bleeding events, as prophylaxis to prevent bleeding events and preserve joint function, and to support surgery in people with haemophilia A. Despite long experience in treating haemophilia A, we are only beginning to understand the functions of FVIII beyond its established role as a coenzyme to factor IXa to expedite thrombin generation through the intrinsic pathway of coagulation. Here, we review the current role of FVIII coagulant (FVIII:C) in haemophilia A management and emerging evidence for the role of FVIII across multiple systems, including the cardiovascular system, angiogenesis and maintenance of bone health. For instance, supraphysiological FVIII levels are a risk factor for venous thromboembolism. von Willebrand factor (VWF), which forms a non-covalent complex with circulating FVIII, is an established marker and regulator of angiogenesis. In a mouse model of haemophilia, treatment with FVIII decreased expression of receptor activator of nuclear factor kappa-Î’ ligand (RANKL), a marker for bone turnover. Longitudinal follow-up data in people with haemophilia A are needed to confirm and extend these observations
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A Neonatal Model of Intravenous Staphylococcus epidermidis Infection in Mice <24 h Old Enables Characterization of Early Innate Immune Responses
Staphylococcus epidermidis (SE) causes late onset sepsis and significant morbidity in catheterized preterm newborns. Animal models of SE infection are useful in characterizing disease mechanisms and are an important approach to developing improved diagnostics and therapeutics. Current murine models of neonatal bacterial infection employ intraperitoneal or subcutaneous routes at several days of age, and may, therefore, not accurately reflect distinct features of innate immune responses to bacteremia. In this study we developed, validated, and characterized a murine model of intravenous (IV) infection in neonatal mice <24 hours (h) old to describe the early innate immune response to SE. C57BL/6 mice <24 h old were injected IV with 106, 107, 108 colony-forming units (CFU) of SE 1457, a clinical isolate from a central catheter infection. A prospective injection scoring system was developed and validated, with only high quality injections analyzed. Newborn mice were euthanized between 2 and 48 h post-injection and spleen, liver, and blood collected to assess bacterial viability, gene expression, and cytokine production. High quality IV injections demonstrated inoculum-dependent infection of spleen, liver and blood. Within 2 h of injection, SE induced selective transcription of TLR2 and MyD88 in the liver, and increased systemic production of plasma IL-6 and TNF-α. Despite clearance of bacteremia and solid organ infection within 48 h, inoculum-dependent impairment in weight gain was noted. We conclude that a model of IV SE infection in neonatal mice <24 h old is feasible, demonstrating inoculum-dependent infection of solid organs and a pattern of bacteremia, rapid and selective innate immune activation, and impairment of weight gain typical of infected human neonates. This novel model can now be used to characterize immune ontogeny, evaluate infection biomarkers, and assess preventative and therapeutic modalities
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