INTERNATIONAL JOURNAL FOR NUMERICAL METHODS IN FLUIDS

Implementation of semi-discrete, non-staggered central schemes in a colocated, polyhedral, finite volume framework, for high-speed viscous flow

A Novel Lifecycle Extension Plan for the Efficient Usage of On-Orbit Post-Consumer Assets

Asteroid mining is a potential form of commercial space industry, and significant amounts of research have gone into the feasibility of that activity. Less research has been done on what happens to the asteroid post-mining; the two primary end-of-life scenarios for the remains of a mined asteroid are not ideal. The remains could be deorbited, which entails complex technical and legal challenges, or they could remain in or-bit, which could lead to collisions and a general increase in space debris. This proposal outlines a solution for the post-consumer asteroid issue which avoids creating more space debris and the risky business of deorbiting. This solution is to use the post-consumer asteroid shell as a shelter for delicate equipment or as a “garbage can in space,” which would hold the remains of defunct satellites until the time they could be more safely deorbited. The shell of the asteroid would provide protection from space debris impacts and some radiation. This proposal also discusses some of the major technical and legal challenges that this solution would face, and how stakeholders could potentially address them. More research is required to gain a better understanding of the challenges and opportunities that this proposal faces, which can be conducted during the long-term development of commercial asteroid mining technologies

The Psychology of Holiness

A series of four lectures delivered April 30th to May 4th, 1951 by Henry Orton Wiley (1877–1961)

Project ATLANTIS (Applied Technology Learning Activities for Non-Traditional Instruction in Space)

As commercial and governmental space endeavors increase in number and complexity, the need for people educated in space policy and law will also grow. In order to create this well-educated group of space professionals, a sophisticated space policy and law curriculum is needed. As accessibility of technology increases and more students are becoming digital natives, the importance of non-traditional curriculums increases. This paper describes an educational experiment in which students in an independent study course created space policy and law educational videos based on topics within the curriculum of an existing undergraduate space law course. Two educational models can be derived from this experiment: the creation of the videos as a special project within a traditional classroom or independent study course, or administering the completed videos as part of a flipped-classroom model. This paper proposes measures of success for both educational models derived from the experiment as well. Beyond engaging students in a flexible, non-traditional curriculum, the benefit of creating the videos was threefold: the activity taught the students the material, developed the digital literacies of the student-creators, and created materials that could be used in a flipped-classroom or a traditional educational setting, or as capacity-building materials. Capacity-building materials are not limited to students at the college levels, but are available through organizations like the United Nations Office of Outer Space Affairs for any situation in which subject matter expertise is lacking. The course materials created in this experiment could be used to complement space law capacity-building materials, for the benefit of all, regardless of gender, generation, or geography. A further benefit to the educational materials made in this project is that they could be used for space law outreach

Writing in Britain and Ireland, c. 400 to c. 800

No abstract available

A Novel Lifecycle Extension Plan for the Efficient Usage of On-Orbit Post-Consumer Assets

Asteroid mining is a highly-discussed emerging area in outer space commercialization. Significant research has gone into the feasibility of asteroid mining, specifically into the retrieval of asteroids and the technical challenges of resource extraction. Less research has focused on the end-of-life of the asteroid. There are two primary end-of-life scenarios for the asteroid: abandonment or deorbit. These scenarios are technologically challenging and potentially risky for the owners of the asteroid. This paper presents a third option for the asteroid asset after mining operations conclude by lengthening the profitable lifespan of the asteroid. Additionally, the plan takes advantage the caverns and depressions in the surface of the asteroid, a byproduct of the resource extraction process. The solution proposed is to use the asteroid as a storage container on orbit for delicate payloads or as a “garbage can in space,” which would hold the remains of defunct space objects. The mass of the asteroid would provide objects stored within passive shielding from the dangers of the space environment. Additional discussion on the major technical and legal challenges that this solution would face, and how stakeholders could potentially address them. This paper presents a third option for the asteroid asset after mining operations conclude. This plan would lengthen the profitable lifespan of the asteroid, thereby avoiding deorbiting the asteroid or abandoning it as space debris. Additionally, the plan takes advantage the caverns and depressions in the surface of the asteroid, a byproduct of the resource extraction process. The solution we propose is to use the asteroid as a storage container on orbit for delicate payloads or as a “garbage can in space,” which would hold the remains of defunct space objects until the time they could be more safely deorbited. The mass of the asteroid would provide objects stored within passive shielding from the dangers of the space environment, namely space debris and radiation. This proposal also discusses some of the major technical and legal challenges that this solution would face, and how stakeholders could potentially address them. More research is required to gain a better understanding of the challenges and opportunities that this proposal faces, which can be conducted during the long-term development of commercial asteroid mining technologies

Signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations and disseminated coccidioidomycosis and histoplasmosis

Background: Impaired signaling in the IFN-g/IL-12 pathway causes susceptibility to severe disseminated infections with mycobacteria and dimorphic yeasts. Dominant gain-of-function mutations in signal transducer and activator of transcription 1 (STAT1) have been associated with chronic mucocutaneous candidiasis. Objective: We sought to identify the molecular defect in patients with disseminated dimorphic yeast infections. Methods: PBMCs, EBV-transformed B cells, and transfected U3A cell lines were studied for IFN-g/IL-12 pathway function. STAT1 was sequenced in probands and available relatives. Interferon-induced STAT1 phosphorylation, transcriptional responses, protein-protein interactions, target gene activation, and function were investigated. Results: We identified 5 patients with disseminated Coccidioides immitis or Histoplasma capsulatum with heterozygous missense mutations in the STAT1 coiled-coil or DNA-binding domains. These are dominant gain-of-function mutations causing enhanced STAT1 phosphorylation, delayed dephosphorylation, enhanced DNA binding and transactivation, and enhanced interaction with protein inhibitor of activated STAT1. The mutations caused enhanced IFN-g–induced gene expression, but we found impaired responses to IFN-g restimulation. Conclusion: Gain-of-function mutations in STAT1 predispose to invasive, severe, disseminated dimorphic yeast infections, likely through aberrant regulation of IFN-g–mediated inflammationFil: Sampaio, Elizabeth P.. National Institutes of Health. National Institute of Allergy and Infectious Diseases. Laboratory of Clinical Infectious Diseases. Immunopathogenesis Section; Estados Unidos. Instituto Oswaldo Cruz. Laboratorio de Leprologia; BrasilFil: Hsu, Amy P.. National Institutes of Health. National Institute of Allergy and Infectious Diseases. Laboratory of Clinical Infectious Diseases. Immunopathogenesis Section; Estados UnidosFil: Pechacek, Joseph. National Institutes of Health. National Institute of Allergy and Infectious Diseases. Laboratory of Clinical Infectious Diseases. Immunopathogenesis Section; Estados UnidosFil: Hannelore I.. National Institutes of Health. National Institute of Allergy and Infectious Diseases. Laboratory of Clinical Infectious Diseases. Immunopathogenesis Section; Estados Unidos. Erasmus Medical Center. Department of Medical Microbiology and Infectious Disease; Países BajosFil: Dias, Dalton L.. National Institutes of Health. National Institute of Allergy and Infectious Diseases. Laboratory of Clinical Infectious Diseases. Immunopathogenesis Section; Estados UnidosFil: Paulson, Michelle L.. Clinical Research Directorate/CMRP; Estados UnidosFil: Chandrasekaran, Prabha. National Institutes of Health. National Institute of Allergy and Infectious Diseases. Laboratory of Clinical Infectious Diseases. Immunopathogenesis Section; Estados UnidosFil: Rosen, Lindsey B.. National Institutes of Health. National Institute of Allergy and Infectious Diseases. Laboratory of Clinical Infectious Diseases. Immunopathogenesis Section; Estados UnidosFil: Carvalho, Daniel S.. National Institutes of Health. National Institute of Allergy and Infectious Diseases. Laboratory of Clinical Infectious Diseases. Immunopathogenesis Section; Estados Unidos. Instituto Oswaldo Cruz, Laboratorio de Leprologia; BrasilFil: Ding, Li. National Institutes of Health. National Institute of Allergy and Infectious Diseases. Laboratory of Clinical Infectious Diseases. Immunopathogenesis Section; Estados UnidosFil: Vinh, Donald C.. McGill University Health Centre. Division of Infectious Diseases; CanadáFil: Browne, Sarah K.. National Institutes of Health. National Institute of Allergy and Infectious Diseases. Laboratory of Clinical Infectious Diseases. Immunopathogenesis Section; Estados UnidosFil: Datta, Shrimati. National Institutes of Health. National Institute of Allergy and Infectious Diseases. Laboratory of Allergic Diseases. Allergic Inflammation Unit; Estados UnidosFil: Milner, Joshua D.. National Institutes of Health. National Institute of Allergy and Infectious Diseases. Laboratory of Allergic Diseases. Allergic Inflammation Unit; Estados UnidosFil: Kuhns, Douglas B.. Clinical Services Program; Estados UnidosFil: Long Priel, Debra A.. Clinical Services Program; Estados UnidosFil: Sadat, Mohammed A.. National Institutes of Health. National Institute of Allergy and Infectious Diseases. Laboratory of Host Defenses. Infectious Diseases Susceptibility Unit; Estados UnidosFil: Shiloh, Michael. University of Texas. Southwestern Medical Center. Division of Infectious Diseases; Estados UnidosFil: De Marco, Brendan. University of Texas. Southwestern Medical Center. Division of Infectious Diseases; Estados UnidosFil: Alvares, Michael. University of Texas. Southwestern Medical Center. Division of Allergy and Immunology; Estados UnidosFil: Gillman, Jason W.. University of Texas. Southwestern Medical Center. Division of Infectious Diseases; Estados UnidosFil: Ramarathnam, Vivek. University of Texas. Southwestern Medical Center. Division of Infectious Diseases; Estados UnidosFil: de la Morena, Maite. University of Texas. Southwestern Medical Center. Division of Allergy and Immunology; Estados UnidosFil: Bezrodnik, Liliana. Gobierno de la Ciudad de Buenos Aires. Hospital General de Niños "Ricardo Gutierrez"; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Moreira, Ileana. Gobierno de la Ciudad de Buenos Aires. Hospital General de Niños "Ricardo Gutierrez"; ArgentinaFil: Uzel, Gulbu. National Institutes of Health. National Institute of Allergy and Infectious Diseases. Laboratory of Clinical Infectious Diseases. Immunopathogenesis Section; Estados UnidosFil: Johnson, Daniel. University of Chicago. Comer Children; Estados UnidosFil: Spalding, Christine. National Institutes of Health. National Institute of Allergy and Infectious Diseases. Laboratory of Clinical Infectious Diseases. Immunopathogenesis Section; Estados UnidosFil: Zerbe, Christa S.. National Institutes of Health. National Institute of Allergy and Infectious Diseases. Laboratory of Clinical Infectious Diseases. Immunopathogenesis Section; Estados UnidosFil: Wiley, Henry. National Eye Institute. Clinical Trials Branch; Estados UnidosFil: Greenberg, David E.. University of Texas. Southwestern Medical Center. Division of Infectious Diseases; Estados UnidosFil: Hoover, Susan E.. University of Arizona. College of Medicine. Valley Fever Center for Excellence; Estados UnidosFil: Rosenzweig, Sergio D.. National Institutes of Health. National Institute of Allergy and Infectious Diseases. Laboratory of Host Defenses Infectious Diseases Susceptibility Unit; Estados Unidos. National Institutes of Health. National Institute of Allergy and Infectious Diseases. Primary Immunodeficiency Clinic; Estados UnidosFil: Galgiani, John N.. University of Arizona. College of Medicine. Valley Fever Center for Excellence; Estados UnidosFil: Holland, Steven M.. National Institutes of Health. National Institute of Allergy and Infectious Diseases. Laboratory of Clinical Infectious Diseases. Immunopathogenesis Section; Estados Unido

Varespladib and cardiovascular events in patients with an acute coronary syndrome: the VISTA-16 randomized clinical trial

IMPORTANCE: Secretory phospholipase A2(sPLA2) generates bioactive phospholipid products implicated in atherosclerosis. The sPLA2inhibitor varespladib has favorable effects on lipid and inflammatory markers; however, its effect on cardiovascular outcomes is unknown. OBJECTIVE: To determine the effects of sPLA2inhibition with varespladib on cardiovascular outcomes. DESIGN, SETTING, AND PARTICIPANTS: A double-blind, randomized, multicenter trial at 362 academic and community hospitals in Europe, Australia, New Zealand, India, and North America of 5145 patients randomized within 96 hours of presentation of an acute coronary syndrome (ACS) to either varespladib (n = 2572) or placebo (n = 2573) with enrollment between June 1, 2010, and March 7, 2012 (study termination on March 9, 2012). INTERVENTIONS: Participants were randomized to receive varespladib (500 mg) or placebo daily for 16 weeks, in addition to atorvastatin and other established therapies. MAIN OUTCOMES AND MEASURES: The primary efficacy measurewas a composite of cardiovascular mortality, nonfatal myocardial infarction (MI), nonfatal stroke, or unstable angina with evidence of ischemia requiring hospitalization at 16 weeks. Six-month survival status was also evaluated. RESULTS: At a prespecified interim analysis, including 212 primary end point events, the independent data and safety monitoring board recommended termination of the trial for futility and possible harm. The primary end point occurred in 136 patients (6.1%) treated with varespladib compared with 109 patients (5.1%) treated with placebo (hazard ratio [HR], 1.25; 95%CI, 0.97-1.61; log-rank P = .08). Varespladib was associated with a greater risk of MI (78 [3.4%] vs 47 [2.2%]; HR, 1.66; 95%CI, 1.16-2.39; log-rank P = .005). The composite secondary end point of cardiovascular mortality, MI, and stroke was observed in 107 patients (4.6%) in the varespladib group and 79 patients (3.8%) in the placebo group (HR, 1.36; 95% CI, 1.02-1.82; P = .04). CONCLUSIONS AND RELEVANCE: In patients with recent ACS, varespladib did not reduce the risk of recurrent cardiovascular events and significantly increased the risk of MI. The sPLA2inhibition with varespladib may be harmful and is not a useful strategy to reduce adverse cardiovascular outcomes after ACS. TRIAL REGISTRATION: clinicaltrials.gov Identifier: NCT01130246. Copyright 2014 American Medical Association. All rights reserved

Disentangling canid howls across multiple species and subspecies: Structure in a complex communication channel.

Wolves, coyotes, and other canids are members of a diverse genus of top predators of considerable conservation and management interest. Canid howls are long-range communication signals, used both for territorial defence and group cohesion. Previous studies have shown that howls can encode individual and group identity. However, no comprehensive study has investigated the nature of variation in canid howls across the wide range of species. We analysed a database of over 2000 howls recorded from 13 different canid species and subspecies. We applied a quantitative similarity measure to compare the modulation pattern in howls from different populations, and then applied an unsupervised clustering algorithm to group the howls into natural units of distinct howl types. We found that different species and subspecies showed markedly different use of howl types, indicating that howl modulation is not arbitrary, but can be used to distinguish one population from another. We give an example of the conservation importance of these findings by comparing the howls of the critically endangered red wolves to those of sympatric coyotes Canis latrans, with whom red wolves may hybridise, potentially compromising reintroduced red wolf populations. We believe that quantitative cross-species comparisons such as these can provide important understanding of the nature and use of communication in socially cooperative species, as well as support conservation and management of wolf populations.Recording work was approved by the Institutional Animal Care and Use Committee of the University of Tennessee. AK is supported by a Herchel Smith postdoctoral fellowship at the University of Cambridge. Part of this work was carried out while AK was a Postdoctoral Fellow at the National Institute for Mathematical and Biological Synthesis, an Institute sponsored by the National Science Foundation through NSF Award #DBI-1300426, with additional support from The University of Tennessee, Knoxville. BH is thankful to the State Forest Departments of Himachal Pradesh, J&K, and Maharashtra, and to various zoos in India for permitting us to record howls. HRG is grateful to all who helped with the project: the staff at Colchester Zoo; the Wildwood Trust, the Borror Laboratory of Bioacoustics; the British Library; Lupus Laetus; Polish Mammal Research Institute; Tigress Productions; the BBC Natural History Unit; Longleat Safari Park; Tierstimmen Archiv; Wild Sweden; Wolf Park; the Macaulay Sound Library and the UK Wolf Conservation Trust; and Mike Collins, Teresa Palmer, Monty Sloan, Karl-Heinz Frommolt, Yorgos Iliopoulos, Christine Anhalt, Louise Gentle, Richard Yarnell, Victoria Allison Hughes and Susan Parks. BRM thanks the USDA/APHIS/WS/National Wildlife Research Center for supporting his doctoral research and providing access to captive coyotes; recording work was approved by the NWRC IACUC. SW thanks Mariana Olsen for assistance with data collection, and Yellowstone National Park for permission to record.This is the author accepted manuscript. The final version is available from Elsevier via http://dx.doi.org/10.1016/j.beproc.2016.01.00

Exercise and bone health across the lifespan

With ageing, bone tissue undergoes significant compositional, architectural and metabolic alterations potentially leading to osteoporosis. Osteoporosis is the most prevalent bone disorder, which is characterised by progressive bone weakening and an increased risk of fragility fractures. Although this metabolic disease is conventionally associated with ageing and menopause, the predisposing factors are thought to be established during childhood and adolescence. In light of this, exercise interventions implemented during maturation are likely to be highly beneficial as part of a long-term strategy to maximise peak bone mass and hence delay the onset of age- or menopause-related osteoporosis. This notion is supported by data on exercise interventions implemented during childhood and adolescence, which confirmed that weight-bearing activity, particularly if undertaken during peripubertal development, is capable of generating a significant osteogenic response leading to bone anabolism. Recent work on human ageing and epigenetics suggests that undertaking exercise after the fourth decade of life is still important, given the anti-ageing effect and health benefits provided, potentially occurring via a delay in telomere shortening and modification of DNA methylation patterns associated with ageing. Exercise is among the primary modifiable factors capable of influencing bone health by preserving bone mass and strength, preventing the death of bone cells and anti-ageing action provided