768 research outputs found

    The relative effect of particles and turbulence on acoustic scattering from deep sea hydrothermal vent plumes revisited

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    Author Posting. © Acoustical Society of America, 2017. This article is posted here by permission of Acoustical Society of America for personal use, not for redistribution. The definitive version was published in Journal of the Acoustical Society of America 141 (2017): 1446–1458, doi:10.1121/1.4974828.The relative importance of suspended particles and turbulence as backscattering mechanisms within a hydrothermal plume located on the Endeavour Segment of the Juan de Fuca Ridge is determined by comparing acoustic backscatter measured by the Cabled Observatory Vent Imaging Sonar (COVIS) with model calculations based on in situ samples of particles suspended within the plume. Analysis of plume samples yields estimates of the mass concentration and size distribution of particles, which are used to quantify their contribution to acoustic backscatter. The result shows negligible effects of plume particles on acoustic backscatter within the initial 10-m rise of the plume. This suggests turbulence-induced temperature fluctuations are the dominant backscattering mechanism within lower levels of the plume. Furthermore, inversion of the observed acoustic backscatter for the standard deviation of temperature within the plume yields a reasonable match with the in situ temperature measurements made by a conductivity-temperature-depth instrument. This finding shows that turbulence-induced temperature fluctuations are the dominant backscattering mechanism and demonstrates the potential of using acoustic backscatter as a remote-sensing tool to measure the temperature variability within a hydrothermal plume.We thank the National Science Foundation for support (NSF Award Nos. OCE-0824612 and OCE-1234163 to APL-UW; NSF Award Nos. OCE-0825088 and OCE-1234141 to Rutgers)

    A preliminary 1-D model investigation of tidal variations of temperature and chlorinity at the Grotto mound, Endeavour Segment, Juan de Fuca Ridge

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    Author Posting. © American Geophysical Union, 2017. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geochemistry, Geophysics, Geosystems 18 (2017): 75–92, doi:10.1002/2016GC006537.Tidal oscillations of venting temperature and chlorinity have been observed in the long-term time series data recorded by the Benthic and Resistivity Sensors (BARS) at the Grotto mound on the Juan de Fuca Ridge. In this study, we use a one-dimensional two-layer poroelastic model to conduct a preliminary investigation of three hypothetical scenarios in which seafloor tidal loading can modulate the venting temperature and chlorinity at Grotto through the mechanisms of subsurface tidal mixing and/or subsurface tidal pumping. For the first scenario, our results demonstrate that it is unlikely for subsurface tidal mixing to cause coupled tidal oscillations in venting temperature and chlorinity of the observed amplitudes. For the second scenario, the model results suggest that it is plausible that the tidal oscillations in venting temperature and chlorinity are decoupled with the former caused by subsurface tidal pumping and the latter caused by subsurface tidal mixing, although the mixing depth is not well constrained. For the third scenario, our results suggest that it is plausible for subsurface tidal pumping to cause coupled tidal oscillations in venting temperature and chlorinity. In this case, the observed tidal phase lag between venting temperature and chlorinity is close to the poroelastic model prediction if brine storage occurs throughout the upflow zone under the premise that layers 2A and 2B have similar crustal permeabilities. However, the predicted phase lag is poorly constrained if brine storage is limited to layer 2B as would be expected when its crustal permeability is much smaller than that of layer 2A.Woods Hole Oceanographic Institution; NOAA; National Science Foundation Grant Numbers: 9820105 , 0120392 , 0701196 , 0751868 , 08190042017-07-1

    ATS-6 spacecraft: In-flight antenna pattern measurement

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    Antenna patterns, principally associated with the 9.1 meter parabolic antenna of the ATS-6 spacecraft, were measured while in orbit at quasi-stationary synchronous altitude. Controlling the spacecraft attitude permitted a scanning of the spacecraft antenna pattern over the Rosman ground station, thus achieving the measurement of the antenna pattern contour. Patterns were determined in terms of relative gain referenced in position to the spacecraft body coordinates by means of signal power measurements made using a linear detector. These data were subsequently correlated with the attitude data to define the antenna patterns. Antenna patterns measured are presented and compared with available preflight patterns

    A Multi-Method Approach for Proteomic Network Inference in 11 Human Cancers.

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    Protein expression and post-translational modification levels are tightly regulated in neoplastic cells to maintain cellular processes known as 'cancer hallmarks'. The first Pan-Cancer initiative of The Cancer Genome Atlas (TCGA) Research Network has aggregated protein expression profiles for 3,467 patient samples from 11 tumor types using the antibody based reverse phase protein array (RPPA) technology. The resultant proteomic data can be utilized to computationally infer protein-protein interaction (PPI) networks and to study the commonalities and differences across tumor types. In this study, we compare the performance of 13 established network inference methods in their capacity to retrieve the curated Pathway Commons interactions from RPPA data. We observe that no single method has the best performance in all tumor types, but a group of six methods, including diverse techniques such as correlation, mutual information, and regression, consistently rank highly among the tested methods. We utilize the high performing methods to obtain a consensus network; and identify four robust and densely connected modules that reveal biological processes as well as suggest antibody-related technical biases. Mapping the consensus network interactions to Reactome gene lists confirms the pan-cancer importance of signal transduction pathways, innate and adaptive immune signaling, cell cycle, metabolism, and DNA repair; and also suggests several biological processes that may be specific to a subset of tumor types. Our results illustrate the utility of the RPPA platform as a tool to study proteomic networks in cancer

    Performance of a 229 Thorium solid-state nuclear clock

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    The 7.8 eV nuclear isomer transition in 229 Thorium has been suggested as an etalon transition in a new type of optical frequency standard. Here we discuss the construction of a "solid-state nuclear clock" from Thorium nuclei implanted into single crystals transparent in the vacuum ultraviolet range. We investigate crystal-induced line shifts and broadening effects for the specific system of Calcium fluoride. At liquid Nitrogen temperatures, the clock performance will be limited by decoherence due to magnetic coupling of the Thorium nucleus to neighboring nuclear moments, ruling out the commonly used Rabi or Ramsey interrogation schemes. We propose a clock stabilization based on counting of flourescence photons and present optimized operation parameters. Taking advantage of the high number of quantum oscillators under continuous interrogation, a fractional instability level of 10^{-19} might be reached within the solid-state approach.Comment: 28 pages, 9 figure

    Nuclear Ground State Observables and QCD Scaling in a Refined Relativistic Point Coupling Model

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    We present results obtained in the calculation of nuclear ground state properties in relativistic Hartree approximation using a Lagrangian whose QCD-scaled coupling constants are all natural (dimensionless and of order 1). Our model consists of four-, six-, and eight-fermion point couplings (contact interactions) together with derivative terms representing, respectively, two-, three-, and four-body forces and the finite ranges of the corresponding mesonic interactions. The coupling constants have been determined in a self-consistent procedure that solves the model equations for representative nuclei simultaneously in a generalized nonlinear least-squares adjustment algorithm. The extracted coupling constants allow us to predict ground state properties of a much larger set of even-even nuclei to good accuracy. The fact that the extracted coupling constants are all natural leads to the conclusion that QCD scaling and chiral symmetry apply to finite nuclei.Comment: 44 pages, 13 figures, 9 tables, REVTEX, accepted for publication in Phys. Rev.

    Proteomic Characterization of Cerebrospinal Fluid from Ataxia-Telangiectasia (A-T) Patients Using a LC/MS-Based Label-Free Protein Quantification Technology

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    Cerebrospinal fluid (CSF) has been used for biomarker discovery of neurodegenerative diseases in humans since biological changes in the brain can be seen in this biofluid. Inactivation of A-T-mutated protein (ATM), a multifunctional protein kinase, is responsible for A-T, yet biochemical studies have not succeeded in conclusively identifying the molecular mechanism(s) underlying the neurodegeneration seen in A-T patients or the proteins that can be used as biomarkers for neurologic assessment of A-T or as potential therapeutic targets. In this study, we applied a high-throughput LC/MS-based label-free protein quantification technology to quantitatively characterize the proteins in CSF samples in order to identify differentially expressed proteins that can serve as potential biomarker candidates for A-T. Among 204 identified CSF proteins with high peptide-identification confidence, thirteen showed significant protein expression changes. Bioinformatic analysis revealed that these 13 proteins are either involved in neurodegenerative disorders or cancer. Future molecular and functional characterization of these proteins would provide more insights into the potential therapeutic targets for the treatment of A-T and the biomarkers that can be used to monitor or predict A-T disease progression. Clinical validation studies are required before any of these proteins can be developed into clinically useful biomarkers
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