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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK; Malden, USA : Blackwell Science Ltd
    European journal of soil science 55 (2004), S. 0 
    ISSN: 1365-2389
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Preservation of organic matter in soils depends on the chemical structure of organic compounds and on the surface properties of the mineral matrix. We tested the effect of mineral surface reactivity on organic matter decomposition by (i) investigating changes of organic matter composition in clay subfractions of an illitic Haplic Chernozem along a time series of fertilizer deprivation and (ii) simultaneously characterizing the reactivity of mineral surfaces. The soil was subjected to fertilizer deprivation for 18, 44 and 98 years, respectively. Mineral surface properties were characterized by selective dissolution of pedogenic oxides. The number of hydroxyls released after exposure to sodium fluoride was taken as an index for mineral surface reactivity. Organic soil constituents were determined by 13C cross-polarization magic-angle spinning nuclear magnetic resonance (13C CPMAS NMR).Clay subfractions had different mineral surface properties. The coarse fractions have more reactive surfaces and contain more organic carbon than the fine clay fractions. Mineral surface properties are constant over time and are not affected by fertilizer deprivation. Surface reactivity is a function of iron oxide density and controls carbon concentrations in the clay subfractions. Within the time frame of our investigation, alkyl C and aromatic C responded to the duration of fertilizer deprivation, but were indifferent to mineral surface reactivity. O–alkyl C seems to be protected by interactions with pedogenic oxides.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK; Malden, USA : Blackwell Science Ltd
    European journal of soil science 56 (2005), S. 0 
    ISSN: 1365-2389
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Soil minerals are known to influence the biological stability of soil organic matter (SOM). Our study aimed to relate properties of the mineral matrix to its ability to protect organic C against decomposition in acid soils. We used the amount of hydroxyl ions released after exposure to NaF solution to establish a reactivity gradient spanning 12 subsoil horizons collected from 10 different locations. The subsoil horizons represent six soil orders and diverse geological parent materials. Phyllosilicates were characterized by X-ray diffraction and pedogenic oxides by selective dissolution procedures. The organic carbon (C) remaining after chemical removal of an oxidizable fraction of SOM with NaOCl solution was taken to represent a stable organic carbon pool. Stable organic carbon was confirmed as older than bulk organic carbon by a smaller radiocarbon (14C) content after oxidation in all 12 soils. The amount of stable organic C did not depend on clay content or the content of dithionite–citrate-extractable Fe. The combination of oxalate-extractable Fe and Al explained the greatest amount of variation in stable organic C (R2 = 0.78). Our results suggest that in acid soils, organic matter is preferentially protected by interaction with poorly crystalline minerals represented by the oxalate-soluble Fe and Al fraction. This evidence suggests that ligand exchange between mineral surface hydroxyl groups and negatively charged organic functional groups is a quantitatively important mechanism in the stabilization of SOM in acid soils. The results imply a finite stabilization capacity of soil minerals for organic matter, limited by the area density of reactive surface sites.
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK; Malden, USA : Blackwell Science Ltd
    European journal of soil science 56 (2005), S. 0 
    ISSN: 1365-2389
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Oxidative treatment can isolate a stable organic matter pool in soils for process studies of organic matter stabilization. Wet oxidation methods using hydrogen peroxide are widely used for that purpose, but are said to modify poorly crystalline soil constituents. We investigated the effect of a modified NaOCl oxidation (pH 8) on the mineral composition of 12 subsoils (4.9–38.2 g organic C kg−1) containing varying amounts of poorly crystalline mineral phases, i.e. 1.1–20.5 g oxalate-extractable Fe kg−1, and of different phyllosilicate mineralogy. Post-oxidative changes in mineral composition were estimated by (i) the determination of elements released into the NaOCl solution, (ii) the difference in dithionite- and oxalate-extractable Si, Al and Fe, and (iii) the specific surface areas (SSAs) of the soils. The NaOCl procedure reduced the organic C concentrations by 12–72%. The amounts of elements released into the NaOCl extracts were small (≤ 0.14 g kg−1 for Si, ≤ 0.13 g kg−1 for Al, and ≤ 0.03 g kg−1 for Fe). The SSA data and the amounts of dithionite- and oxalate-extractable elements suggest that the NaOCl oxidation at pH 8 does not attack pedogenic oxides and hydroxides and only slightly dissolves Al from the poorly crystalline minerals. Therefore, we recommend NaOCl oxidation at pH 8 for the purpose of isolating a stable organic matter pool in soils for process studies of organic matter stabilization.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    European journal of soil science 53 (2002), S. 0 
    ISSN: 1365-2389
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: We used the specific surface area (SSA), the cation exchange capacity (CEC) and the content of dithionite-extractable iron (Fed) to predict the content of organic carbon in illitic clay fractions of topsoils from loess. We determined SSA (BET-N2 method) and CEC of clay fractions after removing organic C or reducing oxides or both. The CEC and the SSA of the carbon- and oxide-free clay fraction explained 56% and 54% of the variation in C content, respectively. The Fed content of the clay fractions was strongly and negatively related to the C content, and with the SSA of the carbon-free clay fraction it predicted C content almost completely (R2 = 0.96). The results indicate that the amount of cations adhering to the silicate clay minerals and the size of the silicate mineral surface area are important properties of the mineral phase for the storage potential of C. The reason for the negative relation between iron oxides and C content remains unclear.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Nuclear Physics, Section A 252 (1975), S. 152-162 
    ISSN: 0375-9474
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Physica D: Nonlinear Phenomena 50 (1991), S. 391-404 
    ISSN: 0167-2789
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Nuclear Inst. and Methods in Physics Research, B 9 (1985), S. 505-508 
    ISSN: 0168-583X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Physics Letters B 43 (1973), S. 98-100 
    ISSN: 0370-2693
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Physics Reports 236 (1994), S. 331-393 
    ISSN: 0370-1573
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Physics Letters B 51 (1974), S. 17-18 
    ISSN: 0370-2693
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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