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  • 1
    ISSN: 1432-0789
    Keywords: Long-term experiment ; Organic fertilization ; Soil organic matter ; Particle-size fractions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary The concentrations of organic C and total N in five different particle-size fractions were studied under different mineral and organic fertilizer regimens by examining soil samples from the 34-year-old soil-formation pot experiment Hu 3 in Rostock. The C and N concentrations were generally highest in the clay fraction and decreased in the order medium silt 〉fine silt 〉coarse silt and sand. For nearly all years and size fractions the following order was obtained for C and N concentrations under the various fertilizer regimens: Compost 〉farmyard manure 〉straw + mineral fertilizer 〉mineral fertilizer. The various particle-size fractions and fertilizer regimens differed in the development of soil organic matter levels. Consequently, characteristic redistributions were found in the proportions of C and N in the various particle-size fractions, particularly after organic fertilizer was no longer applied (years 20–34). This experimental phase was characterized by decreased organic C and increased total N concentrations, and increased proportions of C and N in the clay-size at the expense of the sand fractions.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 50 (1994), S. 844-845 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Biology and fertility of soils 14 (1992), S. 237-245 
    ISSN: 1432-0789
    Keywords: Soil organic matter ; Long-term experiment ; Molecular composition ; Pyrolysis-mass spectrometry ; Grass residues
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary The formation of soil organic matter from grass residues was studied using samples of a long-term experiment (34 years) on humus and soil formation at Rostock, Germany (Hu 3), by elemental analyses (C and N) and pyrolysis-field ionization mass spectrometry of grass residues, humus-free loamy marl, mixtures of this loamy marl with grass roots, and whole soil samples from the 2nd, 7th, 13th, 19th, 25th, 29th, and 34th year of the experiment. The pyrolysis-field ionization mass spectra of the two grass species Phleum pratense and Lolium multiflorum were similar insofar as signals characteristic of lignin dimers and phytosterols dominated at higher masses and for mono-and polysaccharides at lower masses. The most prominent differences between overand underground plant constituents were indicated by higher relative abundances of lignin dimers in the stems and leaves and of sugars and suberin-derived phytosterols in the roots. In the investigation of the influence of mineral to organic matter ratios, comparatively weak effects of the inorganic matrix were obtained: firstly, in the lower mass range (m/z〈250), secondly, for organic matter concentrations between 1.0% and 2.0%, and thirdly, for certain classes of compounds such as phenols, alkanes/alkenes, N heterocycles and mono-and polysaccharides. The qualitative differences in the molecular composition of soil organic matter were clearly attributed to its rapid increase during the first 7 years of the experiment and largely originated from a relative enrichment of lignin dimers. Then, in the period of steady-state soil organic matter levels, dynamic changes were indicated by slight enrichments of mono-and polysaccharides, alkanes/alkenes, fatty acids, N heterocycles, and fluctuating data for phenols/lignin monomers, lignin dimers, and the sum of N compounds. Alkylaromatics showed a steep increase between the 13th and 19th years and remained then on a high level.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-1351
    Keywords: Cochlea ; Outer hair cells ; Echolocation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Isolated outer hair cells (OHCs) and explants ot the organ of Corti were obtained from the cochlea of the echolocating bat, Carollia perspicillata, whose hearing range extends up to about 100 kHz. The OHCs were about 10–30 μm long and produced resting potentials between-30 to -69 mV. During stimulation with a sinusoidal extracellular voltage field (voltage gradient of 2 mV/μm) cyclic length changes were observed in isolated OHCs. The displacements were most prominent at the level of the cell nucleus and the cuticular plate. In the organ of Corti explants, the extracellular electric field induced a radial movement of the cuticular plate which was observed using video subtraction and photodiode techniques. Maximum displacements of about 0.3–0.8 μm were elicited by stimulus frequencies below 100 Hz. The displacement amplitude decreased towards the noise level of about 10–30 nm for stimulus frequencies between 100–500 Hz, both in apical and basal explants. This compares well with data from the guinea pig, where OHC motility induced by extracellular electrical stimulation exhibits a low pass characteristic with a corner frequency below 1 kHz. The data indicate that fast OHC movements presumably are quite small at ultrasonic frequencies and it remains to be solved how they participate in amplifying and sharpening cochlear responses in vivo.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical and applied genetics 79 (1990), S. 575-576 
    ISSN: 1432-2242
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Glycoconjugate journal 10 (1993), S. 327-327 
    ISSN: 1573-4986
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Glycoconjugate journal 10 (1993), S. 287-287 
    ISSN: 1573-4986
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1573-4986
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Glycoconjugate journal 10 (1993), S. 331-331 
    ISSN: 1573-4986
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 620 (1994), S. 665-671 
    ISSN: 0044-2313
    Keywords: Cerium(III) chloride hydrates ; Synthesis ; Solution enthalpies ; Crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Hydrates of Cerium(III) ChlorideThe thermal dehydration of CeCl3 · 7 H2O to CeCl3 gives four definite intermediates: CeCl3 · 6 H2O, CeCl3 · 3 H2O, CeCl3 · 2 H2O, CeCl3 · H2O. In the hexahydrate monomeric [CeCl2(H2O)6]+ units exist. A structure analysis of CeCl3 · 3 H2O gave an orthorhombic unit cell (S.G. Pnma; Z = 4) with a = 1 242.7(4) pm; b = 881.8(8) pm, c = 693.4(5) pm. The structure consists of [CeCl4/2Cl(H2O)3] chains, where two Ce3+ ions are connected via two chloride ions, forming bent chains in the [010] direction. The trihydrates LnCl3 · 3 H2O (Ln = Pr—Tb) are isotypic, also one modification of LaCl3 · 3 H2O. The structures of the di- and mono-hydrate are not yet known. Molar volumina and solution enthalpies in water vary linearly with the number of H2O molecules per formula unit.
    Notes: Der thermische Abbau von CeCl3 · 7 H2O zu CeCl3 verläuft über die präparativ faßbaren Hydrate CeCl3 · 6 H2O, CeCl3 · 3 H2O, CeCl3 · 2 H2O und CeCl3 · H2O. CeCl3 · 6 H2O kristallisiert isotyp zu PrCl3 · 6 H2O mit monomeren [CeCl2(H2O)6]+-Einheiten. Eine Strukturbestimmung von CeCl3 · 3 H2O Pnma; Z = 4; a = 1 242,7(4) pm; b = 881,8(8) pm, c = 693,4(5) pm ergab das Vorliegen von [CeCl4/2Cl(H2O)3]-Einheiten, die über je zwei Chlorid-Doppelbrücken zu gewinkelten Ketten in [010]-Richtung verknüpft sind. Die Trihydrate LnCl3 · 3 H2O (Ln = Pr—Tb) sind isotyp, ebenfalls eine Modifikation von LaCl3 · 3 H2O. Die Strukturen des Di- und Monohydrats sind noch unbekannt. Die Molvolumina und Lösungsenthalpien in Wasser ändern sich linear mit dem Hydratationsgrad.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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