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  • 1970-1974  (7)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 30 (1973), S. 181-193 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Zusammenfassung 1. Es wird bestätigt, daß der Goldfisch entgegen der alten Kreidlschen Annahme (1895) „hört“. Die obere Hörgrenze liegt meist bei g4-c5 (etwa 3000–4000 Hz). 2. Die Pars superior ist lediglich ein statisches Organ und dient entgegen den Manningschen Befunden (1924) nicht zur Schallwahrnehmung. 3. Die Pars inferior dient der Schallperception. Nach ihrer Fortnahme und auch nach der Fortnahme des ganzen Labyrinthes reagiert das Versuchstier nur noch im tiefen Tonbereich bis etwa 250–500 Hz, was dem Hauttastsinn zuzuschreiben ist. 4. Die Dressur mit elektrischen Strafreizen führt bei träge reagierenden Fischen, wie es die Goldfische sind, viel rascher zum Ziel als die Methode der Futterdressur.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Oecologia 9 (1972), S. 215-222 
    ISSN: 1432-1939
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Laboratory populations of the rotifer Brachionus calyciflorus were cultured at different temperatures (25, 20, 15°C) but otherwise at constant conditions. The population densities showed relatively constant oscillations (Figs. 1 to 3A-C). Amplitudes and frequencies of the oscillations were positively correlated with temperature (Table 1). A test was made, whether the logistic growth function with simple time lag is able to describe the population curves. There are strong similarities between the simulations (Figs. 1-3E) and the real population dynamics if minor adjustments of the empirically determined parameters are made. There-fore it is suggested that time lags are responsible for the observed oscillations. However, the actual time lags probably do not act in the simple manner of the model, because birth and death rates react with different time lags, and both parameters are dependent on individual age and population density. A more complex model, which incorporates these modifications, should lead to a more realistic description of the observed oscillations.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 106 (1973), S. 1555-1564 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Pentacarbonyl(organometal selenide)chromium, -molybdenum, and -tungsten ComplexesThe reaction of hexacarbonylchromium, -molybdenum, or -tungsten with bis(trimethylgermyl)selenide, bis(trimethylstannyl)selenide, or bis(trimethylplumbyl)selenide results in the elimination of one CO ligand under formation of the corresponding pentacarbonyl(organometal selenide)chromium(0), -molybdenum(0), or -tungsten(0) complexes (7-15). The i.r., Raman, and 1H n.m.r spectra are discussed.
    Notes: Hexacarbonylchrom, -molybdän und -wolfram reagieren mit Bis(trimethylgermyl)selenid, Bis(trimethylstannyl)selenid und Bis(trimethylplumbyl)selenid unter Abspaltung eines CO-Liganden und Bildung entsprechender Pentacarbonyl(organometallselenid)chrom(0)-, -molyb-dän(0)- bzw -wolfram(0)-Komplexe (7-15). Die Infrarot-, Raman- und 1H-NMR-Spektren werden diskutiert.
    Additional Material: 6 Tab.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 106 (1973), S. 2049-2057 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Pentacarbonyl(organometal telluride)chromium, -molybdenum and -tungsten ComplexesThe reaction of trimethylgermaniumchloride, trimethyltinchloride, or trimethylleadchloride with sodium telluride results in the formation of bis(trimethylgermanium)telluride (1), bis(trimethyltin)telluride (2) or bis(trimethyllead)telluride (3) respectively. These organometaltellurides react with hexacarbonylchromium, hexacarbonylmolybdenum, or hexacarbonyltungsten under elimination of one CO ligand yielding the corresponding pentacarbonyl(organometal telluride)-chromium(0), -molybdenum(0) or -tungsten(0) complexes 4-12. The i.r., Raman, and 1H-n.m.r. spectra are discussed.
    Notes: Trimethylgermanium-, -zinn- und -bleichlorid reagieren mit Natriumtellurid unter Bildung von Bis(trimethylgermyl)- (1), Bis(trimethylstannyl)- (2) und Bis(trimethylplumbyl)tellurid (3). Diese Organometalltelluride bilden mit Hexacarbonylchrom, -molybdän und -wolfram unter Abspaltung eines CO-Liganden entsprechende Pentacarbonyl(organometalltellurid)-chrom(0)-, -molybdän(0)- bzw. -wolfram(0)-Komplexe 4-12. Die IR-, Raman- und 1H-NMR-Spektren werden diskutiert.
    Additional Material: 5 Tab.
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  • 5
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Pyro-field ion mass spectrometry was used to study the primary fragments as well as the depolymerization behaviour of some α-methylstyrene (α-MS) copolymers. α-MS-methyl methacrylate (MMA) copolymers, when pyrolyzed, decompose mainly into the two monomers. The zip-depolymerization usually proceeds through the whole chain, disregarding the hetero-links between different monomeric units. Hetero-fragments are formed only with a small probability; still lower is the concentration of homo-dimers in the pyrolysate.Primary fragments of poly(acrylonitrile) (PAN) are acrylonitrile (AN), (AN)2, (AN)3, HCN, C3H5CN, C4H7CN, C5H9CN and higher nitriles. During pyrolysis of α-MS-AN copolymers, α-MS sequences zipdepolymerize with formation of the monomer. This retropolymerization stops at heterolinks, and fragments of the type α-MS-AN or α-MS-(AN)2 are formed. Long AN sequences in the copolymer cause, as PAN itself, formation of AN oligomeres as well as higher alkene cyanides. Isolated AN units lead to the formation of monomeric AN.
    Notes: Die Pyro-Feldionenmassenspektrometrie wurde zur Untersuchung der Primärfragmente und des Abbauverhaltens von α-Methylstyrol(α-MS)-Copolymeren eingesetzt. α-MS-Methylmethacrylat(MMA)-Copolymere depolymerisieren pyrolytisch unter weitgehender Rückbildung der beiden Monomeren. Die Retropolymerisation („Reißverschlußmechanismus„) geht meist über die Verknüpfungsstellen verschiedener Monomerer hinweg. Heterofragmente (α-MS-MMA) werden nur mit einer geringen Wahrscheinlichkeit gebildet; noch geringer ist die Konzentration von Homodimeren im Pyrolysat.Primärfragmente des Polyacrylnitrils (PAN) sind Acrylnitril (AN), (AN)2, (AN)3, HCN, C3H5CN, C4H7CN, C5H9CN und höhere Nitrile. Bei der Pyrolyse von α-MS-AN-Copolymeren retropolymerisieren α-MS-Sequenzen unter Rückbildung des Monomeren. Die Retropolymerisation macht an Heteroverknüpfungsstellen halt; hierbei bilden sich Heterofragmente des Typs α-MS-AN oder α-MS-(AN)2. Längere AN-Sequenzen im Copolymeren führen bei der Pyrolyse wie bei PAN zu AN-Oligomeren sowie zu höheren Alkencyaniden. Isolierte AN-Einheiten führen zur Bildung von monomerem AN.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 738 (1970), S. 42-45 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On the Bicyclo[3,l,0]hexane-2,4-dione System1,5-Dimethyl-bicyclo[3,l,0]hexane-2,4-dione (5) is prepared by cyclic ester condensation from methyl cis-2-acetyl-1,2-dimethylcyclopropanecarboxylate (4). With 20% enol the pK value amounts to 6.12. Acid cleavage is not found under the influence of alkali. Oxidative degradation leads to cis- 1,2-dimethylcyclopropane-1,2-dicarboxylic acid.
    Notes: 1.5-Dimethyl-bicyclo[3.l.0]hexandion-(2.4) (5) wird durch cyclisierende Esterkondensation aus cis-2-Acetyl-l.2-dimethyl-cyclopropancarbonsäure-methylester (4) hergestellt. Bei einem Enol-Gehalt von 20% beträgt der pK-Wert 6.12. Bei der Einwirkung von Alkali kann keine Säurespaltung beobachtet werden. Der oxydative Abbau ergibt cis-1.2-Dimethyl-cyclopropandicarbonsäure-(1.2).
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