204 research outputs found

    British Wartime Control of Prices

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    Sensing Through the Continent: Towards Monitoring Migratory Birds Using Cellular Sensor Networks

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    This paper presents CraneTracker, a novel sensor platform for monitoring migratory birds. The platform is designed to monitor Whooping Cranes, an endangered species that conducts an annual migration of 4, 000 km between southern Texas and north-central Canada. CraneTracker includes a rich set of sensors, a multi-modal radio, and power control circuitry for sustainable, continental-scale information delivery during migration. The need for large-scale connectivity motivates the use of cellular technology in low-cost sensor platforms augmented by a low-power transceiver for ad-hoc connectivity. This platform leads to a new class of cellular sensor networks (CSNs) for time-critical and mobile sensing applications. The CraneTracker is evaluated via field tests on Wild Turkeys, Siberian Cranes, and an on-going alpha deployment with wild Sandhill Cranes. Experimental evaluations demonstrate the potential of energy-harvesting CSNs for wildlife monitoring in large geographical areas, and reveal important insights into the movements and behaviors of migratory animals. In addition to benefiting ecological research, the developed platform is expected to extend the application domain of sensor networks and enable future research applications

    Multiwavelength Observations of the Second Largest Known FR II Radio Galaxy, NVSS 2146+82

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    We present multi-frequency VLA, multicolor CCD imaging, optical spectroscopy, and ROSAT HRI observations of the giant FR II radio galaxy NVSS 2146+82. This galaxy, which was discovered by the NRAO VLA Sky Survey (NVSS), has an angular extent of nearly 20' from lobe to lobe. The radio structure is normal for an FR II source except for its large size and regions in the lobes with unusually flat radio spectra. Our spectroscopy indicates that the optical counterpart of the radio core is at a redshift of z=0.145, so the linear size of the radio structure is ~4 h_50^-1 Mpc. This object is therefore the second largest FR II known (3C 236 is ~6 h_50^-1 Mpc). Optical imaging of the field surrounding the host galaxy reveals an excess number of candidate galaxy cluster members above the number typically found in the field surrounding a giant radio galaxy. WIYN HYDRA spectra of a sample of the candidate cluster members reveal that six share the same redshift as NVSS 2146+82, indicating the presence of at least a ``rich group'' containing the FR II host galaxy. ROSAT HRI observations of NVSS 2146+82 place upper limits on the X-ray flux of 1.33 x 10^-13 ergs cm^-2 s^-1 for any hot IGM and 3.52 x 10^-14 ergs cm^-2 s^-1 for an X-ray AGN, thereby limiting any X-ray emission at the distance of the radio galaxy to that typical of a poor group or weak AGN. Several other giant radio galaxies have been found in regions with overdensities of nearby galaxies, and a separate study has shown that groups containing FR IIs are underluminous in X-rays compared to groups without radio sources. We speculate that the presence of the host galaxy in an optically rich group of galaxies that is underluminous in X-rays may be related to the giant radio galaxy phenomenon.Comment: 46 pages, 15 figures, AASTeX aaspp4 style, accepted for publication in A

    The role of measuring exhaled breath biomarkers in sarcoidosis: A systematic review

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    Introduction: Sarcoidosis is a chronic granulomatous disease of unknown aetiology with a variable clinical course and prognosis. There is a growing need to identify non-invasive biomarkers to differentiate between clinical phenotypes, identify those at risk of disease progression and monitor response to treatment. Objectives: We undertook a systematic review and meta-analysis, to evaluate the utility of breath-based biomarkers in discriminating sarcoidosis from healthy controls, alongside correlation with existing non-breath based biomarkers used in clinical practice, radiological stage, markers of disease activity and response to treatment. Methods: Electronic searches were undertaken during November 2017 using PubMed, Ebsco, Embase and Web of Science to capture relevant studies evaluating breath-based biomarkers in adult patients with sarcoidosis. Results: 353 papers were screened; 21 met the inclusion criteria and assessed 25 different biomarkers alongside VOCs in exhaled breath gas or condensate. Considerable heterogeneity existed amongst the studies in terms of participant characteristics, sampling and analytical methods. Elevated biomarkers in sarcoidosis included 8-isoprostane, carbon monoxide, neopterin, TGF-β1, TNFα, CysLT and several metallic elements including chromium, silicon and nickel. Three studies exploring VOCs were able to distinguish sarcoidosis from controls. Meta-analysis of four studies assessing alveolar nitric oxide showed no significant difference between sarcoidosis and healthy controls (2.22ppb; 95% CI -0.83, 5.27) however, a high degree of heterogeneity was observed with an I2 of 93.4% (p<0.001). Inconsistent or statistically insignificant results were observed for correlations between several biomarkers and radiological stage, markers of disease activity or treatment. Conclusions: The evidence for using breath biomarkers to diagnose and monitor sarcoidosis remains inconclusive with many studies limited by small sample sizes and lack of standardisation. VOCs have shown promising potential but further research is required to evaluate their prognostic role

    Safety and pharmacokinetics of multiple dose myo-inositol in preterm infants

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    BACKGROUND: Preterm infants with respiratory distress syndrome (RDS) given inositol had reduced bronchopulmonary dysplasia (BPD), death and severe retinopathy of prematurity (ROP). We assessed the safety and pharmacokinetics of daily inositol to select a dose providing serum levels previously associated with benefit, and to learn if accumulation occurred when administered throughout the normal period of retinal vascularization. METHODS: Infants ≤ 29 wk GA (n = 122, 14 centers) were randomized and treated with placebo or inositol at 10, 40, or 80 mg/kg/d. Intravenous administration converted to enteral when feedings were established, and continued to the first of 10 wk, 34 wk postmenstrual age (PMA) or discharge. Serum collection employed a sparse sampling population pharmacokinetics design. Inositol urine losses and feeding intakes were measured. Safety was prospectively monitored. RESULTS: At 80 mg/kg/d mean serum levels reached 140 mg/l, similar to Hallman's findings. Levels declined after 2 wk, converging in all groups by 6 wk. Analyses showed a mean volume of distribution 0.657 l/kg, clearance 0.058 l/kg/h, and half-life 7.90 h. Adverse events and comorbidities were fewer in the inositol groups, but not significantly so. CONCLUSION: Multiple dose inositol at 80 mg/kg/d was not associated with increased adverse events, achieves previously effective serum levels, and is appropriate for investigation in a phase III trial

    Formulation of a mmaA4 Gene Deletion Mutant of Mycobacterium bovis BCG in Cationic Liposomes Significantly Enhances Protection against Tuberculosis

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    A new vaccination strategy is urgently needed for improved control of the global tuberculosis (TB) epidemic. Using a mouse aerosol Mycobacterium tuberculosis challenge model, we investigated the protective efficacy of a mmaA4 gene deletion mutant of Mycobacterium bovis BCG (ΔmmaA4BCG) formulated in dimethyl dioctadecyl ammonium bromide (DDA) – D(+) trehalose 6,6 dibenenate (TDB) (DDA/TDB) adjuvant. In previous studies, deletion of the mmaA4 gene was shown to reduce the suppression of IL-12 production often seen after mycobacterial infections. While the non-adjuvanted ΔmmaA4BCG strain did not protect mice substantially better than conventional BCG against a tuberculous challenge in four protection experiments, the protective responses induced by the ΔmmaA4BCG vaccine formulated in DDA/TDB adjuvant was consistently increased relative to nonadjuvanted BCG controls. Furthermore, the ΔmmaA4BCG-DDA/TDB vaccine induced significantly higher frequencies of multifunctional (MFT) CD4 T cells expressing both IFNγ and TNFα (double positive) or IFNγ, TNFα and IL-2 (triple positive) than CD4 T cells derived from mice vaccinated with BCG. These MFT cells were characterized by having higher IFNγ and TNFα median fluorescence intensity (MFI) values than monofunctional CD4 T cells. Interestingly, both BCG/adjuvant and ΔmmaA4BCG/adjuvant formulations induced significantly higher frequencies of CD4 T cells expressing TNFα and IL-2 than nonadjuvanted BCG or ΔmmaA4BCG vaccines indicating that BCG/adjuvant mixtures may be more effective at inducing central memory T cells. Importantly, when either conventional BCG or the mutant were formulated in adjuvant and administered to SCID mice or immunocompromised mice depleted of IFNγ, significantly lower vaccine-derived mycobacterial CFU were detected relative to immunodeficient mice injected with non-adjuvanted BCG. Overall, these data suggest that immunization with the ΔmmaA4BCG/adjuvant formulation may be an effective, safe, and relatively inexpensive alternative to vaccination with conventional BCG

    LSST Science Book, Version 2.0

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    A survey that can cover the sky in optical bands over wide fields to faint magnitudes with a fast cadence will enable many of the exciting science opportunities of the next decade. The Large Synoptic Survey Telescope (LSST) will have an effective aperture of 6.7 meters and an imaging camera with field of view of 9.6 deg^2, and will be devoted to a ten-year imaging survey over 20,000 deg^2 south of +15 deg. Each pointing will be imaged 2000 times with fifteen second exposures in six broad bands from 0.35 to 1.1 microns, to a total point-source depth of r~27.5. The LSST Science Book describes the basic parameters of the LSST hardware, software, and observing plans. The book discusses educational and outreach opportunities, then goes on to describe a broad range of science that LSST will revolutionize: mapping the inner and outer Solar System, stellar populations in the Milky Way and nearby galaxies, the structure of the Milky Way disk and halo and other objects in the Local Volume, transient and variable objects both at low and high redshift, and the properties of normal and active galaxies at low and high redshift. It then turns to far-field cosmological topics, exploring properties of supernovae to z~1, strong and weak lensing, the large-scale distribution of galaxies and baryon oscillations, and how these different probes may be combined to constrain cosmological models and the physics of dark energy.Comment: 596 pages. Also available at full resolution at http://www.lsst.org/lsst/sciboo

    Review: Far-infrared instrumentation and technological development for the next decade

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    This work is licensed under a Creative Commons Attribution 4.0 Unported License.Far-infrared astronomy has advanced rapidly since its inception in the late 1950s, driven by a maturing technology base and an expanding community of researchers. This advancement has shown that observations at far-infrared wavelengths are important in nearly all areas of astrophysics, from the search for habitable planets and the origin of life to the earliest stages of galaxy assembly in the first few hundred million years of cosmic history. The combination of a still-developing portfolio of technologies, particularly in the field of detectors, and a widening ensemble of platforms within which these technologies can be deployed, means that far-infrared astronomy holds the potential for paradigm-shifting advances over the next decade. We examine the current and future far-infrared observing platforms, including ground-based, suborbital, and space-based facilities, and discuss the technology development pathways that will enable and enhance these platforms to best address the challenges facing far-infrared astronomy in the 21st century
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