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  • 2015-2019  (291)
  • 1985-1989  (89)
  • 1950-1954  (14)
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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 26 (1954), S. 726-727 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 90 (1986), S. 5956-5959 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 529 (1988), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Polar research 5 (1987), S. 0 
    ISSN: 1751-8369
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geography , Geosciences
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Zeitschrift für angewandte Mathematik und Physik 1 (1950), S. 185-189 
    ISSN: 1420-9039
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mathematics , Physics
    Notes: Summary It is well known that the dominant latent root of a square (real or complex) matrix may be calculated by iteration of the matrix on punched-card machines provided this root is single. The present paper treats the problem of the calculation of the derivatives of that root with respect to the elements of the matrix, It is shown that these derivatives may be calculated in short time without punching additional cards by simple permutation of the cards already used in the iteration process.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    International journal of earth sciences 75 (1986), S. 805-827 
    ISSN: 1437-3262
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Description / Table of Contents: Abstract Carbonate preservation profiles in the Atlantic Ocean and the Norwegian-Greenland Sea seem to be out-of phase during the last deglaciation. A possibly time transgressive deglacial preservation spike in the N-Atlantic overlaps with a major calcite dissolution pulse in the Norwegian Sea. Contemporaneously major changes in surface and bottom water circulation of the Norwegian-Greenland Sea occurred. Isotopic and sedimentological evidence suggests that bottom water formation in the Norwegian-Greenland Sea was almost shut down during the last maximum glaciation and probably also during the first part of the last deglaciation. During that time corrosive bottom waters might have filled the Norwegian Sea deep sea basins causing carbonate dissolution at the sea floor. Subsequently, the reinitiation of deep water formation could have been coupled with increased resuspension of organic matter and/or reworking of older organic matter rising the p CO2 of bottom waters and contributing to carbonate dissolution at the sea floor. Additionally, large volumes of atmospheric CO2 stored before the Younger Dryas might have been pumped into the deep sea possibly by downwelling of surface waters and been neutralized against carbonate at the sea floor.
    Abstract: Résumé Au moyen den l'examen des foraminifères planctoniquesN. pachyderma, des profils de l'état de conservation des carbonates ont été établis dans les sédiments déposés dans l'Atlantique et dans la Mer de Norvège au cours de la phase de fusion de la dernière glaciation. Ces profils ne sont pas en corrélation: dans l'Atlantique apparaÎt un maximum de stabilité des carbonates, probablement transgressif dans le temps, qui correspond à une phase de forte dissolution dans la Mer de Norvège. Certains paramètres sédimentologiques (granularité, teneur en C organique, structures sédimentaires) ainsi que des variations de la composition isotopique de l'O et du C des foraminifères benthoniques permettent de penser que la production d'eau profonde s'est arrÊtée dans la Mer de Norvège au cours du maximum de la dernière glaciation et sans doute aussi pendant le début de la fusion qui a suivi. Pendant cette période, le mélange vertical des masses d'eau était fortement ralenti et une ancienne eau de fond à caractère corrosif occupait le bassin de la Mer de Norvège où elle induisait une forte dissolution des carbonates. Plus tard, lorsque se rétablirent la circulation de l'eau de fond et la formation d'eau profonde, on assita à une aération de la partie profonde de la mer, par l'effet de la descente d'eau superficielle riche en oxygène. L'oxydation de la matière organique provoqua un accroissement de la pression partielle de CO2 dans l'eau de fond, ce qui y accentua la dissolution des carbonates. Une autre source possible pourrait Être le CO2 accumulé dans l'atmosphère avant le Dryas supérieur et entraÎné vers la profondeur par la descente des eaux de surface.
    Notes: Zusammenfassung Erhaltungsprofile des Karbonatlösungszustandes, bestimmt an der planktonischen Foraminif ere N. pachyderma aus Sedimenten, die während der letzten Abschmelzphase der letzten Eiszeit abgelagert wurden, zeigen im Atlantik und in der Norwegisch-Grönländischen See eine deutliche Phasenverschiebung der Erhaltungszustände. Ein möglicherweise zeittransgressiver Erhaltungspeak im Atlantik tritt in zeitlicher überlappung mit einer Phase erhöhter Karbonatlösung in der Norwegischen See auf. Aufgrund verschiedener sedimentologischer Parameter (Korngrö\enspektren, C-org Gehalte, Sedimentstrukturen) und deutlicher Veränderungen der stabilen Sauerstoff- und Kohlenstoffisotopenverhältnisse benthonischer Foraminiferen erscheint es wahrscheinlich, da\ die Tiefenwasserproduktion in der Norwegisch-Grönländischen See während des Höchststandes der letzten Vereisung und möglicherweise auch während des ersten Abschnittes des Abschmelzvorgangs gestoppt war. Während dieses Zeitraumes war die vertikale Durchmischung der Wassermassen stark herabgesetzt und altes korrosives Bodenwasser füllte die Tiefseebecken der Norwegischen See und verursachte eine intensive Karbonatlösung am Meeresboden. Nachdem die Bodenwasserzirkulation und Tiefenwasserbildung später erneut einsetzte, wurde zunächst eine verstärkte Ventilation durch absinkendes, sauerstoffreiches Oberflächenwasser am Meeresboden verursacht. Die Oxidation von resuspendiertem und die Aufarbeitung von bereits abgelagertem organischem Material bedingte einen letzten starken Anstieg des CO2 Partialdrucks im Bodenwasser und verstärkte die Karbonatlösung am Meeresboden. Eine mögliche zusätzliche Quelle liefert vor der Jüngeren Dryas in der Atmosphäre angereichertes CO2, das möglicherweise durch »downwelling« von Oberflächenwasser zusätzlich in die Tiefsee gepumpt wurde.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Physics and chemistry of minerals 14 (1987), S. 396-400 
    ISSN: 1432-2021
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Abstract A number of surface sensitive electron spectroscopic techniques have been used during the last few years to study the geometric and electronic structure of well characterized surfaces of metal oxide single crystals. For rocksalt monoxides, the (100) surface has been found to be very nearly a truncation of the bulk lattice; only qualitativelow energy electron diffraction (LEED) measurements have been performed on other oxide crystal structures. The electronic structure of nearly perfect oxide surfaces is generally very similar to that of the bulk, although excitonic surface states have been found on some rocksalt oxides. However, the presence of O-vacancy point defects on transition metal oxide surfaces changes their electronic structure drastically, increasing the d-orbital population of the cations adjacent to the defect. These surface defects are generally the active sites for chemisorption, with nearly perfect surfaces being relatively inert with respect to most of the molecules that have been studied.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1432-1904
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1617-4623
    Keywords: pepD gene ; gpt gene ; Intergenic region ; lpcA locus ; Peptidase D purification
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary A cloned DNA fragment, carrying the gene for peptidase D (pepD) of Escherichia coli, was partially sequenced. By purification of peptidase D and sequence determination of an amino-terminal oligopeptide the reading frame of the pepD gene, starting with a GTG initiator codon, was unambiguously identified. An overlap of the established nucleotide sequence with the previously sequenced 5′ flanking region of the gpt gene allowed the exact distance between pepD and gpt to be calculated. The two genes are pointing towards each other and are separated by 260 bp. A search for open reading frames (ORFs) and the analysis of possible codon usage in the intercistronic region indicate the absence of an additional gene (lpcA) between pepD and gpt.
    Type of Medium: Electronic Resource
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