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  • 1
    Series available for loan
    Series available for loan
    Stockholm
    Associated volumes
    Call number: SR 93.0768(500)
    In: Sveriges Geologiska Undersökning
    Type of Medium: Series available for loan
    Pages: 16 S.
    Series Statement: Sveriges geologiska undersökning : Ser. C, Avhandlingar och uppsatser 500
    Language: Swedish
    Location: Lower compact magazine
    Branch Library: GFZ Library
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  • 2
    Monograph available for loan
    Monograph available for loan
    Washington, DC : National Aeronautics and Space Administration
    Call number: G 8956 ; G 8956(2. Ex., Fanselau)
    Type of Medium: Monograph available for loan
    Pages: XII, 599 S. : graph. Darst.
    Series Statement: NASA SP 345
    Location: Upper compact magazine
    Location: Upper compact magazine
    Branch Library: GFZ Library
    Branch Library: GFZ Library
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  • 3
    Monograph non-lending collection
    Monograph non-lending collection
    Leipzig : Akad. Verl.-Ges.
    Call number: H O 218
    Type of Medium: Monograph non-lending collection
    Pages: VI, 208 S. : Ill.
    Uniform Title: Världarnas utveckling
    Language: German
    Location: Pendulum room
    Branch Library: GFZ Library
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  • 4
    Monograph available for loan
    Monograph available for loan
    Leipzig : Akad. Verl.-Ges.
    Call number: MOP 5382
    Type of Medium: Monograph available for loan
    Pages: VI, 208 S. : Ill., graph. Darst.
    Location: MOP - must be ordered
    Branch Library: GFZ Library
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  • 5
    Publication Date: 1994-02-01
    Print ISSN: 0169-6149
    Electronic ISSN: 1573-0875
    Topics: Biology , Geosciences
    Published by Springer
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  • 6
    Publication Date: 2019-07-13
    Description: The sources and speciation of reduced carbon and nitrogen inferred for the early Archean are reviewed in terms of current observations and models, and known chemical reactions. Within this framework hydrogen cyanide and cyanide ion in significant concentration would have been eliminated by reaction with excess formaldehyde to form cyanohydrin (glycolonitrile), and with ferrous ion to formferrocyanide. Natural reactions of these molecules would under such conditions deserve special consideration in modeling of primordial organochemical processes. As a step in this direction, transformation reactions have been investigated involving glycolonitrile in the presence of water. We find that glycolonitrile, formed from formaldehyde and hydrogen cyanide or cyanide ion, spontaneously cyclodimerizes to 4-amino-2-hydroxymethyloxazole. The crystalline dimer is the major product at low temperatue (approximately 0 C); the yield diminishes with increasing temperature at the expense of polymerization and hydrolysis products. Hydrolysis of glycolamide and of oxazole yields a number of simpler organic molecules, including ammonia and glycolamide. The spontaneous polymerization of glycolonitrile and its dimer gives rise to soluble, cationic oligomers of as yet unknown structure, and, unless arrested, to a viscous liquid, insoluble in water. A loss of cyanide by reaction with formaldehyde, inferred for the early terrestrial hydrosphere and cryosphere would present a dilemma for hypotheses invoking cyanide and related compounds as concentrated reactants capable of forming biomolecular precursor species. Attempts to escape from its horns may take advantage of the efficient concentration and separation of cyanide as solid ferriferrocyanide, and most directly of reactions of glycolonitrile and its derivatives.
    Keywords: GEOPHYSICS
    Type: Origins of Life and Evolution of the Biosphere (ISSN 0169-6149); 24; 1; p. 1-17
    Format: text
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  • 7
    Publication Date: 2019-08-27
    Description: A central problem in molecular evolution concerns the selective concentration from dilute, multicomponent solution of source molecules into a reactive environment, where formation of larger molecular assemblages can take place. Minerals consisting of positively charged, separable metal hydroxide sheets have proven capable of these functions. This common structural type is represented by minerals such as pyroaurite (Mg-Fe(3+) hydroxide), hydrotalcite (Mg-Al), green rust Fe(2+)-Fe(3+) and others. Effective interlayer sorption is demonstrated for orthophosphate and condensed phosphates, anionic alkyl compounds, polypeptides, nucleic acids, cyanide complexes and glycolaldehyde phosphate, the latter shown to readily oligomerize to form and selectively retain racemic hexose -2, 4, 6-phosphates, preferentially of altrose (Pitsch, et al, 1993). The selective aldomerization and retention effects correlate with the charge distribution in the host mineral structure and the stereochemistry of the substrate molecules. Interaction between nucleic acid bases, and between the cyanide groups of glycolaldehyde phosphate nitrile at the low water activity in the mineral interlayer is indicated by doubling of the monomeric separation of the hydroxide mineral sheets.
    Keywords: LIFE SCIENCES (GENERAL)
    Type: Origins of Life and Evolution of the Biosphere (ISSN 0169-6149); 24; 4-Feb; p. 336
    Format: text
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Origins of life and evolution of the biospheres 24 (1994), S. 1-17 
    ISSN: 1573-0875
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Geosciences
    Notes: Abstract The sources and speciation of reduced carbon and nitrogen inferred for the early Archean are reviewed in terms of current observations and models, and known chemical reactions. Within this framework hydrogen cyanide and cyanide ion in significant concentration would have been eliminated by reaction with excess formaldehyde to form cyanohydrin (glycolonitrile), and with ferrous ion to form ferrocyanide. Natural reactions of these molecules would under such conditions deserve special consideration in modeling of primordial organochemical processes. As a step in this direction, transformation reactions have been investigated involving glycolonitrile in the presence of water. We find that glycolonitrile, formed from formaldehyde and hydrogen cyanide or cyanide ion, spontaneously cyclodimerizes to 4-amino-2-hydroxymethyloxazole. The crystalline dimer is the major product at low temperature (∼0 °C); the yield diminishes with increasing temperature at the expense of polymerization and hydrolysis products. Hydrolysis of glycolonitrile and of oxazole yields a number of simpler organic molecules, including ammonia and glycolamide. The spontaneous polymerization of glycolonitrile and its dimer gives rise to soluble, cationic oligomers of as yet unknown structure, and, unless arrested, to a viscous liquid, insoluble in water. A loss of cyanide by reaction with formaldehyde, inferred for the early terrestrial hydrosphere and cryosphere would present a dilemma for hypotheses invoking cyanide and related compounds as concentrated reactants capable of forming biomolecular precursor species. Attempts to escape from its horns may take advantage of the efficient concentration and separation of cyanide as solid ferriferrocyanide, and most directly of reactions of glycolonitrile and its derivatives.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Astrophysics and space science 144 (1988), S. 357-372 
    ISSN: 1572-946X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Alfvén in his early work on the origin of the solar system (1942–1946) noted a pronounced band structure in the gravitational potential distribution of secondary bodies, and suggested this feature to be directly related to the formation process. When the critical velocity phenomenon was later discovered, a close agreement was found between the planet-satellite bands on one hand, and the critical velocity limits of the major compound elements in the interstellar medium on the other, suggesting a specific emplacement mechanism for the dusty plasma which presumably constituted the solar nebula. Since the originally perceived band structure was outlined in a qualitative fashion, an attempt is made here to analyze the distribution by a statistical technique, testing the significance of clustering of the observational data in the bands. The results show that, with proper scaling of the parameters, such a band structure indeed appears, with features closely similar to those originally conceived. Some deviations are indicated by the cluster analysis, however; their significance is discussed in terms of process involved in the formation of the solar system.
    Type of Medium: Electronic Resource
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  • 10
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    Unknown
    PANGAEA
    In:  Supplement to: Goldberg, Edward D; Arrhenius, Gustaf (1958): Chemistry of Pacific pelagic sediments. Geochimica et Cosmochimica Acta, 13(2-3), 153-212, https://doi.org/10.1016/0016-7037(58)90046-2
    Publication Date: 2023-08-28
    Description: The chemical and mineralogical composition of pelagic sediments from the East Pacific Ocean has been determined with the aim of defining the ultimate sources and the mechanisms of formation of the solid phases. The distribution of elements between sea-water, the pore solution and the various solid components of the sediments permits interpretations of the variations in time and space of the gross chemical composition of pelagic clays. For example, manganese, present in sea-water in a divalent form, is apparently oxidized at the sediment-water interface to tetravalent species which subsequently become a part of the group of ferromanganese oxide minerals which are found in the marine environment. It is suggested the rate of manganese accumulation in sediments is some function of the length of time the sediment surface is in contact with sea-water. The contribution of chemical species from the different geospheres is considered. The quantitative importance of pelagic clays in the major sedimentary cycle is studied on the basis of the distribution of the weathered igneous rock products between continental and pelagic deposits and sea-water. These analyses of a wide variety of pelagic clays allow a reformulation of the geochemical balance and it is concluded that pelagic clays account for approximately 13 per cent of the total mass of sediments produced over geologic time.
    Keywords: 08995002-SC11; Barium; Boron; Calcium; Chromium; Cobalt; Copper; DEPTH, sediment/rock; Description; Dredge; DRG; File name; Magnesium; Manganese; Nickel; NOAA and MMS Marine Minerals Geochemical Database; NOAA-MMS; Sample ID; San Clemente Basin, Pacific ocean; Strontium; Tin; Titanium; Uniform resource locator/link to image; Vanadium; X-ray microanalyzer analysis (XMA); Ytterbium; Zirconium
    Type: Dataset
    Format: text/tab-separated-values, 30 data points
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