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  • 1
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Key engineering materials Vol. 157-158 (May 1998), p. 113-120 
    ISSN: 1013-9826
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1793
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Phylogenetic relationships among the seven species of deep-sea giant clams Calyptogena (Bivalvia: Vesicomyidae) collected around Japan were examined using parts of nucleotide sequences of mitochondrial genes for cytochrome oxidase I (COI) and cytochrome oxidase III (COIII) and the encoded amino acid sequences. The seven species were C. soyoae (Sagami Bay), C. fausta (Suruga Bay), C. kaikoi (Nankai Trough), C. nautilei (Nankai Trough), C. phaseoliformis (Japan Trench), C. solidissima (Minami-Ensei Knoll, Okinawa Trough) and Calyptogena sp. (Iheya Ridge, Okinawa Trough). A clear phylogenetic split was observed between one group of three species (C. kaikoi, C. phaseoliformis and C. fausta) and the remaining species. This clustering corresponds to the two previously described subgenera within the genus Calyptogena (Calyptogean and Ectenagena) with the exception of the placement of C. nautilei, which had been placed in the subgenus Ectenagena. Genetic distances between two haplotypes of C. soyoae were 0.043 for the COI region and 0.055 for the COIII region, and three amino acid substitutions were detected with the COIII region. Calyptogena sp. from the Iheya Ridge could be distinguished from one of the two haplotypes (type A) of C. soyoae by only a single nucleotide substitution, a result that suggests that Calyptogena sp. of the Iheya Ridge diverged from C. soyoae after the two haplotypes had diverged, and it is now isolated from C. soyoae in Sagami Bay.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Biology and fertility of soils 24 (1997), S. 261-265 
    ISSN: 1432-0789
    Keywords: Key words Methane ; Wetland rice soils ; Oryza sativa ; Methane oxidation ; Acetylene Propylene oxide ; Methanotrophs ; Rhizosphere
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Acetylene up to 500 μl l–1 did not affect methane formation in anoxic soil up to 12 h, but further incubation for 1 week showed strong inhibition of methanogenesis. To ascertain the extent of the oxidation of methane produced from rice-planted pots, the effect of acetylene on methane emission was studied. Two rice varieties (Toyohatamochi and Yamahikari) were grown in a greenhouse in submerged soil in pots. At about maximum tillering, heading, and grain-forming stages, methane fluxes were measured. Flux measurement was performed for 3 h from 6 pm, then acetylene at 100 μl l–1 was added to some of the pots. At 6 a.m. the following day, methane fluxes were again measured for 3 h. Only at maximum tillering stage of the variety Toyohatamochi was a significant increase (1.4 times) in methane flux caused by acetylene observed, whereas in the other treatments no significant increase in methane fluxes by acetylene could be defected. To ascertain the activity of methane monooxygenase (MMO), propylene oxide (PPO) formation from propylene was measured with excised roots and a basal portion of stems of the rice plants grown on the submerged soil. A level of 0.1–0.2 μmol PPO h–1 plant–1 was recorded. The roots showed the highest PPO formation per gram dry matter, followed by basal stems. Methane oxidation was roughly proportional to PPO formation. Soluble MMO-positive methanotroph populations were measured by plate counts. The number of colony-forming units per gram dry matter was 106–105 in roots, and 104–103 in basal stems. These results indicate the possibility of methane oxidation in association with wetland rice plants.
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  • 4
    ISSN: 1432-0789
    Keywords: Methane oxidation ; Propylene oxide ; Wetland rice soils ; Methanotrophs ; Methane monooxygenase ; Greenhouse effect
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract The magnitude of methane emission is a net result of methane production and the oxidation rate. The possibility of measuring oxidized products of alternative substrates of methane monooxygenase was examined to determine methane-oxidizing ability of soils, and to count methanotrophic populations in soils. Wetland rice soils were incubated under methane containing air to enirch the methanotrophs. Methane loss and oxygen uptake were inhibited by acetylene, dimethylether, and nitrapyrin (N-Serve). Acetylene was used routinely, because it inhibited methane oxidation even at a low concentration of 0.03 to 0.06 μl ml-1 in the incubation headspace. Propylene at 10 kPa was used as an alternative substrate of methane monooxygenase, and the formation of propylene oxide was measured. When soils were incubated under methane, their methane-oxidizing activity increased. Propylene oxide formation increased simultaneously. Acetylene also blocked propylene oxidation. The results of several experiments and propylene oxide formation (r=0.87 after long-transformation). These results indicate that propylene oxide formation can be used as a semiquantitative measure of the methane-oxidizing activity of soils. The colonies of soluble methane monooxygenase-forming methanotrophs were counted on Cu-deficient methanotroph agar medium by the formation of naphthol from haphthalene. The counts increased from 104 (0 days) to 107 (21 days) g-1 soil during oxic incubation under methane.
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  • 5
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 52 (1996), S. 405-406 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Crystals of aldehyde reductase from a red yeast, Sporobolomyces salmonicolor, have been grown from an ammonium sulfate solution, pH 7.0, by means of the vapor-diffusion procedure. The crystals belong to the hexagonal system, space group P6122 or its enantiomorph, P6522, with unit-cell dimensions of a = 72.2 and c = 320 Å. The X-ray diffraction patterns extend to at least 2 Å resolution with the use of synchrotron radiation. The crystals are stable on exposure to X-rays and suitable for high-resolution X-ray structure determination.
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 801 (1996), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 104 (1996), S. 6244-6258 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Multireference perturbation theory with complete active space self-consistent field (CASSCF) reference functions was applied to the study of the valence π→π* excited states of benzene and naphthalene. The eigenvectors and eigenvalues of CASSCF with valence π active orbitals satisfy pairing properties for the alternant hydrocarbons to a good approximation. The excited states of polyacenes are classified into the covalent minus states and ionic plus states with the use of the alternancy symmetry. The present theory satisfactorily describes the ordering of low-lying valence π→π* excited states. The overall accuracy of the present approach is surprisingly high. We were able to predict the valence excitation energies with an accuracy of 0.27 eV for singlet u states and of 0.52 eV or better for singlet g states of naphthalene. Our predicted triplet states spectrum provides a consistent assignment of the triplet–triplet absorption spectrum of naphthalene. For benzene we were able to predict the valence excitation energy with an accuracy of about 0.29 eV. The covalent minus states and ionic plus states exhibit different behavior as far as the electron correlation is concerned. The ionic plus states are dominated by the single excitations but covalent minus states include a large fraction of doubly excited configurations. The covalent minus states always give lower energy than the corresponding ionic plus states. This is true for triplet states. The dynamic σ–π polarization effects introduced by perturbation theory are significant for the ionic plus states while those on covalent excited states are usually of the same order as in the covalent ground state. The enlargement of the active space of the reference functions represents a great improvement of the description of the ionic states. The present approach with the pairing properties has proved to be of great value in understanding and predicting the experimental data of the alternant hydrocarbons. © 1996 American Institute of Physics.
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  • 8
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 82 (1997), S. 3593-3597 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The magnetization-curling mode in a columnar-structure film with perpendicular magnetization is studied on the assumption that the film is a two-dimensional array of cylinders. The angular dependence of the nucleation field HN is calculated by the Ritz method and compared with that for the coherent-rotation mode. It is found that the magnetization rotates in the curling mode for a large reduced radius S and in the coherent-rotation mode for a small S. The angular dependence of HN is different from that in an infinite cylinder. If S is large, the magnetization rotates in the curling mode for any value of θ0, where θ0 is the angle between the applied field and the cylinder axis. When S is medium, the magnetization rotates in the coherent-rotation mode for a small θ0 and in the curling mode for a large θ0. © 1997 American Institute of Physics.
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  • 9
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 78 (1995), S. 7410-7412 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The heat capacity of the ternary compounds RNiGe(R=Er, Dy, Gd, and Y) was studied in the temperature range between 2 and 40 K. From the heat capacity curves, Néel temperatures are found to be 3.3, 7.4, and 10.7 K for ErNiGe, DyNiGe, and GdNiGe, respectively. The heat capacity of YNiGe was well fitted with an average Debye temperature of 272 K in the temperature range between 2 and 40 K. The changes of magnetic entropy indicate a strong influence of the crystal field on the Er+3 and Dy+3 ion in ErNiGe and DyNiGe compounds. These results suggest the possibility of using these compounds as magnetic regenerator materials near the temperature of 4.2 K. © 1995 American Institute of Physics.
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  • 10
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 77 (1995), S. 2214-2216 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: To search the new magnetic regenerator materials in the temperature range near 4 K, specific heat behavior of pseudobinary compounds ErxDy1−xSb(x=0, 0.2, 0.6, 0.8, and 1) was studied at temperatures from 2 to 40 K. The ordering temperature shifts from 3.5 to 9.5 K with increasing the concentration of the Dy+3 ion. The compounds of 1(approximately-greater-than)x(approximately-greater-than)0 show the gradual magnetic phase transition. The change of entropy associated with the magnetic phase transition is close to R ln 2 for all compounds. The change of magnetic entropy up to 40 K increases rapidly with decreasing the concentration of the Dy+3 ion, which implies that more excited states exist. The compounds of lower concentration of the Dy+3 ion have properties well suited for magnetic regenerative material around the temperature range of 4 K. © 1995 American Institute of Physics.
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