Phosphorus loss from soil to water.

End of Project ReportThe work described under this project covers field work on phosphorus(P) loss from soil to water under field conditions. In addition two International Workshops on P loss to water, held in Ireland in 1995 and 1998, are also covered under this project. The results indicate that P loss to water is a complex process and it is influenced by a number of factors, including hydrology of the soil, rates and timing of P application and soil P levels. Most work on this subject indicates that there is a positive relationship between soil test P levels and P loss to water. There is need for further work to establish the relative contribution of the different variables involved in P loss from soil to water for different soils and farming conditions. This should help provide answers to the most sustainable methods to minimise losses of P to water and ensure that agricultural production is compatible with good water quality.European Union Structural Funds (EAGGF

Exoplanet Detection Synenergy Between Gaia and the WFIRST Coronagraph

Future astrometric detections of exoplanets from the Gaia mission will augment and improve the sample of targets accessible to the Coronagraph Instrument (CGI) on WFIRST. We assessed the joint detection sensitivity of Gaia and WFIRST by modeling random planet populations around nearby (d less than 20 pc), bright (V less than 6) stars, and applying nominal detection thresholds for each mission. Our analysis suggests that only a small number of the new planet detections from Gaia will be favorable for spectroscopic characterization by WFIRST CGI: 1-3 planets, depending on the assumed planet population model. The target stars hosting gas giants detectable to both missions tend to be GK dwarfs with brightness between V = 3-5, and distances within 10 pc. While few in number, these new Gaia-detected exoplanets could be exceptionally valuable targets for WFIRST due to the ability to incorporate astrometric mass estimates into the spectral retrieval of atmospheric parameters

Specification of advanced safety modeling requirements (Rev. 0).

The U.S. Department of Energy's Global Nuclear Energy Partnership has lead to renewed interest in liquid-metal-cooled fast reactors for the purpose of closing the nuclear fuel cycle and making more efficient use of future repository capacity. However, the U.S. has not designed or constructed a fast reactor in nearly 30 years. Accurate, high-fidelity, whole-plant dynamics safety simulations will play a crucial role by providing confidence that component and system designs will satisfy established design limits and safety margins under a wide variety of operational, design basis, and beyond design basis transient conditions. Current modeling capabilities for fast reactor safety analyses have resulted from several hundred person-years of code development effort supported by experimental validation. The broad spectrum of mechanistic and phenomenological models that have been developed represent an enormous amount of institutional knowledge that needs to be maintained. Complicating this, the existing code architectures for safety modeling evolved from programming practices of the 1970s. This has lead to monolithic applications with interdependent data models which require significant knowledge of the complexities of the entire code in order for each component to be maintained. In order to develop an advanced fast reactor safety modeling capability, the limitations of the existing code architecture must be overcome while preserving the capabilities that already exist. To accomplish this, a set of advanced safety modeling requirements is defined, based on modern programming practices, that focuses on modular development within a flexible coupling framework. An approach for integrating the existing capabilities of the SAS4A/SASSYS-1 fast reactor safety analysis code into the SHARP framework is provided in order to preserve existing capabilities while providing a smooth transition to advanced modeling capabilities. In doing this, the advanced fast reactor safety models will target leadership-class computing architectures for massively-parallel high-fidelity computations while providing continued support for rapid prototyping using modest fidelity computations on multiple-core desktop platforms

Elucidation of the RamA Regulon in Klebsiella pneumoniae Reveals a Role in LPS Regulation

Klebsiella pneumoniae is a significant human pathogen, in part due to high rates of multidrug resistance. RamA is an intrinsic regulator in K. pneumoniae established to be important for the bacterial response to antimicrobial challenge; however, little is known about its possible wider regulatory role in this organism during infection. In this work, we demonstrate that RamA is a global transcriptional regulator that significantly perturbs the transcriptional landscape of K. pneumoniae, resulting in altered microbe-drug or microbe-host response. This is largely due to the direct regulation of 68 genes associated with a myriad of cellular functions. Importantly, RamA directly binds and activates the lpxC, lpxL-2 and lpxO genes associated with lipid A biosynthesis, thus resulting in modifications within the lipid A moiety of the lipopolysaccharide. RamA-mediated alterations decrease susceptibility to colistin E, polymyxin B and human cationic antimicrobial peptide LL-37. Increased RamA levels reduce K. pneumoniae adhesion and uptake into macrophages, which is supported by in vivo infection studies, that demonstrate increased systemic dissemination of ramA overexpressing K. pneumoniae. These data establish that RamA-mediated regulation directly perturbs microbial surface properties, including lipid A biosynthesis, which facilitate evasion from the innate host response. This highlights RamA as a global regulator that confers pathoadaptive phenotypes with implications for our understanding of the pathogenesis of Enterobacter, Salmonella and Citrobacter spp. that express orthologous RamA proteins

Methods for Quantifying Uncertainty in Fast Reactor Analyses.

Liquid-metal-cooled fast reactors in the form of sodium-cooled fast reactors have been successfully built and tested in the U.S. and throughout the world. However, no fast reactor has operated in the U.S. for nearly fourteen years. More importantly, the U.S. has not constructed a fast reactor in nearly 30 years. In addition to reestablishing the necessary industrial infrastructure, the development, testing, and licensing of a new, advanced fast reactor concept will likely require a significant base technology program that will rely more heavily on modeling and simulation than has been done in the past. The ability to quantify uncertainty in modeling and simulations will be an important part of any experimental program and can provide added confidence that established design limits and safety margins are appropriate. In addition, there is an increasing demand from the nuclear industry for best-estimate analysis methods to provide confidence bounds along with their results. The ability to quantify uncertainty will be an important component of modeling that is used to support design, testing, and experimental programs. Three avenues of UQ investigation are proposed. Two relatively new approaches are described which can be directly coupled to simulation codes currently being developed under the Advanced Simulation and Modeling program within the Reactor Campaign. A third approach, based on robust Monte Carlo methods, can be used in conjunction with existing reactor analysis codes as a means of verification and validation of the more detailed approaches

Myosin-X functions in polarized epithelial cells

Myosin-X, an unconventional myosin that has been studied primarily in fibroblast-like cells, has been shown to have important functions in polarized epithelial cell junction formation, regulation of paracellular permeability, and epithelial morphogenesis.Myosin-X (Myo10) is an unconventional myosin that localizes to the tips of filopodia and has critical functions in filopodia. Although Myo10 has been studied primarily in nonpolarized, fibroblast-like cells, Myo10 is expressed in vivo in many epithelia-rich tissues, such as kidney. In this study, we investigate the localization and functions of Myo10 in polarized epithelial cells, using Madin-Darby canine kidney II cells as a model system. Calcium-switch experiments demonstrate that, during junction assembly, green fluorescent protein–Myo10 localizes to lateral membrane cell–cell contacts and to filopodia-like structures imaged by total internal reflection fluorescence on the basal surface. Knockdown of Myo10 leads to delayed recruitment of E-cadherin and ZO-1 to junctions, as well as a delay in tight junction barrier formation, as indicated by a delay in the development of peak transepithelial electrical resistance (TER). Although Myo10 knockdown cells eventually mature into monolayers with normal TER, these monolayers do exhibit increased paracellular permeability to fluorescent dextrans. Importantly, knockdown of Myo10 leads to mitotic spindle misorientation, and in three-dimensional culture, Myo10 knockdown cysts exhibit defects in lumen formation. Together these results reveal that Myo10 functions in polarized epithelial cells in junction formation, regulation of paracellular permeability, and epithelial morphogenesis