Nitridogermanate Nitrides Sr7[GeN4]N2 and Ca7[GeN4]N2

The alkaline earth nitridogermanate nitrides AE7[GeN4]N2 (AE = Ca, Sr) have been synthesized using a Na flux technique in sealed Ta tubes. According to single-crystal X-ray diffraction the isotypic compounds crystallize in space group Pbcn (No. 60) with Z = 4, (Sr7[GeN4]N2: a = 1152.6(2), b = 658.66(13), c = 1383.6(3) pm, V = 1050.5(4) × 106 pm3, R1 = 0.049; Ca7[GeN4]N2: a = 1082.6(2), b = 619.40(12), c = 1312.1(3) pm, V = 879.8(3) × 106 pm3, R1 = 0.016). Owing to the high N/Ge ratio, the compounds contain discrete N3− ions coordinated by six AE2+ besides discrete [GeN4]8− tetrahedrons. One of the AE2+ ion is coordinated by only four N3− ions, which is rather an unusual low coordination number for Sr2+. Together with the isolated [GeN4]8− tetrahedrons, these Sr2+ ions form chains of alternating cation centered edge sharing tetrahedrons. The electronic structure and chemical bonding in Sr7[GeN4]N2 has been analyzed employing linear muffin-tin orbital (LMTO) band structure calculations

Spacecraft nitrogen generation

Two spacecraft nitrogen (N2) generation systems based on the catalytic dissociation of hydrazine (N2H4) were evaluated. In the first system, liquid N2H4 is catalytically dissociated to yield an N2 and hydrogen (H2) gas mixture. Separation of the N2/H2 gas mixture to yield N2 and a supply of H2 is accomplished using a polymer-electrochemical N2/H2 separator. In the second system, the N2/H2 gas mixture is separated in a two-stage palladium/silver (Pd/Ag) N2/H2 separator. The program culminated in the successful design, fabrication, and testing of a N2H4 catalytic dissociator, a polymer-electrochemical N2/H2 separator, and a two-stage Pd/Ag N2/H2 separator. The hardware developed was sized for an N2 delivery rate of 6.81 kg/d (15lb/day). Experimental results demonstrated that both spacecraft N2 generation systems are capable of producing 6.81 kg/d (15lb/day) of 99.9% pure N2 at a pressure greater than or equal to 1035 kN/m(2) (150 psia)

Operator-Schmidt decomposition of the quantum Fourier transform on C^N1 tensor C^N2

Operator-Schmidt decompositions of the quantum Fourier transform on C^N1 tensor C^N2 are computed for all N1, N2 > 1. The decomposition is shown to be completely degenerate when N1 is a factor of N2 and when N1>N2. The first known special case, N1=N2=2^n, was computed by Nielsen in his study of the communication cost of computing the quantum Fourier transform of a collection of qubits equally distributed between two parties. [M. A. Nielsen, PhD Thesis, University of New Mexico (1998), Chapter 6, arXiv:quant-ph/0011036.] More generally, the special case N1=2^n1<2^n2=N2 was computed by Nielsen et. al. in their study of strength measures of quantum operations. [M.A. Nielsen et. al, (accepted for publication in Phys Rev A); arXiv:quant-ph/0208077.] Given the Schmidt decompositions presented here, it follows that in all cases the communication cost of exact computation of the quantum Fourier transform is maximal.Comment: 9 pages, LaTeX 2e; No changes in results. References and acknowledgments added. Changes in presentation added to satisfy referees: expanded introduction, inclusion of ommitted algebraic steps in the appendix, addition of clarifying footnote

Input of nitrogen from N2 fixation to northern grasslands

Forage legumes form N2-fixing symbioses with rhizobia and may thus make substantial contributions to the N pool in grasslands. However, to optimize their use as sources of N, it is important to elucidate the effects of management factors that influence their N2 fixation rates, and to develop convenient methods for measuring N2 fixation quickly and reliably. An analysis of published data on N2 fixation in the field showed that lucerne (Medicago sativa L.), red clover (Trifolium pratense L.), and white clover (T. repens L.) grown in mixtures with grasses derived most of their N from N2 fixation, irrespective of geographic location and management practices – and despite large inter-annual variations in legume dry matter yield (kg ha-1 year-1). Consequently, there were strong correlations between legume dry matter yield and amounts of N2 fixed (kg N ha-1 year-1), which can be used very simply to obtain estimates of N2 fixation in these legumes. In experimental grassland plots where the species richness of neighbouring vegetation was varied, alsike clover (T. hybridum L.), red clover, and white clover consistently derived at least half of their N from N2 fixation, measured by the 15N natural abundance (NA) method using three different reference plants. This method is sensitive to the degree of discrimination against 15N in the N2-fixing plant (B value) and the choice of reference plant. B values were therefore established for each of the three clover species in symbioses with different Scandinavian Rhizobium leguminosarum bv. trifolii genotypes. In red clover, reductions following cutting in the activity of the N2-fixing enzyme, nitrogenase, and the rate of shoot regrowth were dependent on the cutting height. The recovery in nitrogenase activity after cutting followed the rate of leaf area increment, which confirms the correlation between N2 fixation and growth found in field experiments. The results of the work underlying this thesis show that perennial forage legumes growing in grasslands are highly dependent on N2 fixation. Awareness of this should facilitate the development of resource-efficient management regimes for northern grasslands

Gauge invariant formulation of N=2N=2 Toda and KdV systems in extended superspace

We give a gauge invariant formulation of $N=2$ supersymmetric abelian Toda field equations in \n2 superspace. Superconformal invariance is studied. The conserved currents are shown to be associated with Drinfeld-Sokolov type gauges. The extension to non-abelian \n2 Toda equations is discussed. Very similar methods are then applied to a matrix formulation in \n2 superspace of one of the \n2 KdV hierarchies.Comment: 21 page

Nitrogen Fixation Mutants of the Actinobacterium Frankia Casuarinae CcI3

Frankia is a representative genus of nitrogen-fixing (N2-fixing) actinobacteria; however, the molecular mechanisms underlying various phenomena such as the differentiation of a N2 fixation-specific structure (vesicle) and the regulation of N2 fixation (nif) genes, have yet to be elucidated in detail. In the present study, we screened hyphal fragments of Frankia casuarinae that were mutagenized by 1-methyl-3-nitro-1-nitrosoguanidine or gamma rays, and isolated 49 candidate N2 fixation mutants. Twelve of these mutants were selected for further study, and their abilities to grow in NH3-deficient (N-) liquid media and their rates of acetylene reduction activities were evaluated. Eleven mutant strains were confirmed to lack the ability to fix N2. Five mutant strains formed significantly reduced numbers of vesicles, while some failed to form large mature vesicles. These vesicle mutants also exhibited an aberrant hyphal morphology, suggesting a relationship between vesicle differentiation and hyphal branching. Ten mutants showed significant reductions in the expression of nifE, nifH, and nifV genes under N- conditions. The genome sequencing of eight mutants identified 20 to 400 mutations. Although mutant strains N3H4 and N6F4 shared a large number of mutations (108), most were unique to each strain. Mutant strain N7C9 had 3 mutations in the nifD and nifH genes that may result in the inability to fix N2. The other mutant strains did not have any mutations in any known N2 fixation-related genes, indicating that they are novel N2 fixation mutants

Hopanoid lipids may facilitate aerobic nitrogen fixation in the ocean.

Cyanobacterial diazotrophs are considered to be the most important source of fixed N2 in the open ocean. Biological N2 fixation is catalyzed by the extremely O2-sensitive nitrogenase enzyme. In cyanobacteria without specialized N2-fixing cells (heterocysts), mechanisms such as decoupling photosynthesis from N2 fixation in space or time are involved in protecting nitrogenase from the intracellular O2 evolved by photosynthesis. However, it is not known how cyanobacterial cells limit O2 diffusion across their membranes to protect nitrogenase in ambient O2-saturated surface ocean waters. Here, we explored all known genomes of the major marine cyanobacterial lineages for the presence of hopanoid synthesis genes, since hopanoids are a class of lipids that might act as an O2 diffusion barrier. We found that, whereas all non-heterocyst-forming cyanobacterial diazotrophs had hopanoid synthesis genes, none of the marine Synechococcus, Prochlorococcus (non-N2-fixing), and marine heterocyst-forming (N2-fixing) cyanobacteria did. Finally, we conclude that hopanoid-enriched membranes are a conserved trait in non-heterocyst-forming cyanobacterial diazotrophs that might lower the permeability to extracellular O2 This membrane property coupled with high respiration rates to decrease intracellular O2 concentration may therefore explain how non-heterocyst-forming cyanobacterial diazotrophs can fix N2 in the fully oxic surface ocean

Production of N2 Vegard-Kaplan and other triplet band emissions in the dayglow of Titan

Recently the Cassini Ultraviolet Imaging Spectrograph has revealed the presence of N2 Vegard-Kaplan band emissions in Titan's dayglow limb observation. We present model calculations for the production of various N2 triplet states in the upper atmosphere of Titan. The Analytical Yield Spectra technique is used to calculate steady state photoelectron fluxes in Titan's atmosphere, which are in agreement with those observed by the Cassini's CAPS instrument. Considering direct electron impact excitation, inter-state cascading, and quenching effects, the population of different levels of N2 triplet states are calculated under statistical equilibrium. Densities of all vibrational levels of each triplet state and volume production rates for various triplet states are calculated in the model. Vertically integrated overhead intensities for the same date and lighting conditions as the reported by UVIS observations for N2 VK, 1P, 2P, Wu-Benesch, and Reverse First Positive bands of N2 are found to be 132, 114, 19, 22, and 22 R, respectively. Overhead intensities are calculated for each vibrational transition of all the triplet band emissions of N2, which span a wider spectrum of wavelengths from ultraviolet to infrared. The calculated limb intensities of total and prominent transitions of VK band are presented. The model limb intensity of VK emission within the 150-190 nm wavelength region is in good agreement with the Cassini UVIS observed limb profile. An assessment of the impact of solar EUV flux on the N2 triplet band emission intensity has been made by using three different solar flux models, viz., Solar EUV Experiment, SOLAR2000 model of Tobiska (2004), and HEUVAC model of Richards et al, (2006). The calculated N2 VK band intensity at the peak of limb intensity due to S2K and HEUVAC solar flux models is a factor of 1.2 and 0.9, respectively, of that obtained using SEE solar EUV flux.Comment: 25 pages, 11 figures; Icarus, 201