TY - JOUR A1 - Kaiser, Michael A1 - Zederer, Dan P. A1 - Ellerbrock, Ruth H. A1 - Sommer, Michael A1 - Ludwig, Bernard T1 - Effects of mineral characteristics on content, composition, and stability of organic matter fractions separated from seven forest topsoils of different pedogenesis JF - Geoderma : an international journal of soil science N2 - Mineral topsoils possess large organic carbon (OC) contents but there is only limited knowledge on the mechanisms controlling the preservation of organic matter (OM) against microbial decay. Samples were taken from the uppermost mineral topsoil horizon (0 to 5 cm) of seven sites under mature deciduous forest showing OC contents between 69 and 164 g kg(-1) and a wide range in mineral characteristics. At first, organic particles and the water-extractable OM were removed from the soil samples. Thereafter, Na-pyrophosphate extractable organic matter (OM(PY)), assumed to be indicative for OM bound via cation mediated interactions, and the OM remaining in the extraction residue (OM(ER)), supposed to be indicative for OM occluded in mechanically highly stable micro-aggregates, were sequentially separated and quantified. The composition of OM(PY) and OM(ER) was analyzed by FTIR and their stability by C-14 measurements. The OC remaining in the extraction residues accounted for 38 to 59% of the bulk soil OC (SOC) suggesting a much larger relevance of OM(ER) for the OM dynamic in the analyzed soils as compared with OM(PY) that accounted for 1.6 to 7.5% of the SOC. The FUR analyses revealed a lower relative proportion of C=O groups in OM(ER) compared to OM(PY) indicating differences in the degree of microbial processing between these fractions. Correlation analyses suggest an increase in the stability of OM(PY) with the soil pH and contents of Na-pyrophosphate soluble Fe, Al, and Mg and an increase in the stability of OM(ER) with the soil pH and the contents of clay and oxalate-soluble Fe and Al. Despite the detected influence of soil mineral characteristics on the turnover of OM(PY) and OM(ER), the Delta C-14 signatures indicated mean residence times less than 100 years. The presence of less stabilized OM in these fractions can be derived from methodological uncertainties and/or the fast cycling compartment of mineral-associated OM. (C) 2015 Elsevier B.V. All rights reserved. KW - Forest mineral topsoil KW - Organic matter stabilization KW - Na-pyrophosphate soluble organic matter KW - Micro-aggregates KW - Infrared spectroscopy KW - C-14 analyses Y1 - 2016 U6 - https://doi.org/10.1016/j.geoderma.2015.08.029 SN - 0016-7061 SN - 1872-6259 VL - 263 SP - 1 EP - 7 PB - Elsevier CY - Amsterdam ER - TY - JOUR A1 - Kayler, Z. E. A1 - Kaiser, Michael A1 - Gessler, A. A1 - Ellerbrock, Ruth H. A1 - Sommer, Michael T1 - Application of delta C-13 and delta N-15 isotopic signatures of organic matter fractions sequentially separated from adjacent arable and forest soils to identify carbon stabilization mechanisms JF - Biogeosciences N2 - Identifying the chemical mechanisms behind soil carbon bound in organo-mineral complexes is necessary to determine the degree to which soil organic carbon is stabilized belowground. Analysis of delta C-13 and delta N-15 isotopic signatures of stabilized OM fractions along with soil mineral characteristics may yield important information about OM-mineral associations and their processing history. We anlayzed the delta C-13 and delta N-15 isotopic signatures from two organic matter (OM) fractions along with soil mineral proxies to identify the likely binding mechanisms involved. We analyzed OM fractions hypothesized to contain carbon stabilized through organo-mineral complexes: (1) OM separated chemically with sodium pyrophosphate (OM(PY)) and (2) OM occluded in micro-structures found in the chemical extraction residue (OM(ER)). Because the OM fractions were separated from five different soils with paired forest and arable land use histories, we could address the impact of land use change on carbon binding and processing mechanisms. We used partial least squares regression to analyze patterns in the isotopic signature of OM with established mineral and chemical proxies indicative for certain binding mechanisms. We found different mechanisms predominate in each land use type. For arable soils, the formation of OM(PY)-Ca-mineral associations was identified as an important OM binding mechanism. Therefore, we hypothesize an increased stabilization of microbial processed OM(PY) through Ca2+ interactions. In general, we found the forest soils to contain on average 10% more stabilized carbon relative to total carbon stocks, than the agricultural counter part. In forest soils, we found a positive relationship between isotopic signatures of OM(PY) and the ratio of soil organic carbon content to soil surface area (SOC/SSA). This indicates that the OM(PY) fractions of forest soils represent layers of slower exchange not directly attached to mineral surfaces. From the isotopic composition of the OM(ER) fraction, we conclude that the OM in this fraction from both land use types have undergone a different pathway to stabilization that does not involve microbial processing, which may include OM which is highly protected within soil micro-structures. Y1 - 2011 U6 - https://doi.org/10.5194/bg-8-2895-2011 SN - 1726-4170 VL - 8 IS - 10 SP - 2895 EP - 2906 PB - Copernicus CY - Göttingen ER - TY - JOUR A1 - Kaiser, Michael A1 - Walter, K. A1 - Ellerbrock, Ruth H. A1 - Sommer, Michael T1 - Effects of land use and mineral characteristics on the organic carbon content, and the amount and composition of Na-pyrophosphate-soluble organic matter, in subsurface soils JF - European journal of soil science N2 - Land use and mineral characteristics affect the ability of surface as well as subsurface soils to sequester organic carbon and their contribution to mitigation of the greenhouse effect. There is less information about the effects of land use and soil properties on the amount and composition of organic matter (OM) for subsurface soils as compared with surface soils. Here we aimed to analyse the long-term (>= 100 years) impact of arable and forest land use and soil mineral characteristics on subsurface soil organic carbon (SOC) contents, as well as on amount and composition of OM sequentially separated by Na pyrophosphate solution (OM(PY)) from subsurface soil samples. Seven soils with different mineral characteristics (Albic and Haplic Luvisol, Colluvic and Haplic Regosol, Haplic and Vertic Cambisol, Haplic Stagnosol) were selected from within Germany. Soil samples were taken from subsurface horizons of forest and adjacent arable sites continuously used for > 100 years. The OM(PY) fractions were analysed for their OC content (OC(PY)) and characterized by Fourier transform infrared spectroscopy. Multiple regression analyses for the arable subsurface soils indicated significant positive relationships between the SOC contents and combined effects of the (i) exchangeable Ca (Ca(ex)) and oxalate-soluble Fe (Fe(ox)) and (ii) the Ca(ex) and Al(ox) contents. For these soils the increase in OC (OC(PY) multiplied by the relative C=O content of OM(PY)) and increasing contents of Ca(ex) indicated that OM(PY) mainly interacts with Ca2+. For the forest subsurface soils (pH < 5), the OC(PY) contents were related to the contents of Na-pyrophosphate-soluble Fe and Al. The long-term arable and forest land use seems to result in different OM(PY)-mineral interactions in subsurface soils. On the basis of this, we hypothesize that a long-term land-use change from arable to forest may lead to a shift from mainly OM(PY)-Ca2+ to mainly OM(PY)-Fe3+ and -Al3+ interactions if the pH of subsurface soils significantly decreases to < 5. Y1 - 2011 U6 - https://doi.org/10.1111/j.1365-2389.2010.01340.x SN - 1351-0754 VL - 62 IS - 2 SP - 226 EP - 236 PB - Wiley-Blackwell CY - Malden ER - TY - JOUR A1 - Kaiser, M. A1 - Ellerbrock, Ruth H. A1 - Wulf, M. A1 - Dultz, S. A1 - Hierath, C. A1 - Sommer, M. T1 - The influence of mineral characteristics on organic matter content, composition, and stability of topsoils under long-term arable and forest land use JF - Journal of geophysical research : Biogeosciences N2 - In this study, we analyzed the influence of soil mineral characteristics (e. g., clay concentration and mineralogical composition, iron and aluminum oxide concentration and crystallinity, specific surface area, and exchangeable cation concentration) on (i) organic carbon (OC) content (kg m(-2)) and (ii) the concentration (g kg(-1)), composition, and stability of the mineral-associated organic matter (OM) of arable and forest topsoils. We selected seven soil types with different mineral characteristics for this study. For each soil type, samples were taken from topsoils of a deciduous forest and an adjacent arable site. The arable and forest sites have been used continuously for more than 100 years. Na-pyrophosphate soluble OM fractions (OM(PY)), representing mineral-associated OM, were extracted, analyzed for OC and C-14 concentrations, and characterized by FTIR spectroscopy. For the forest and arable topsoils, a linear relationship was found between the OC content and exchangeable Ca. For the arable topsoils (pH 6.7-7.5), correlation analyses indicated that the OCPY concentration increased with an increase in oxalate soluble Fe and Al, exchangeable Ca, and Na-pyrophosphate soluble Mg and Fe concentrations. The stability of OM(PY) determined by the C-14 measurements of the near-neutral arable topsoils was shown to increase with the specific surface area and the concentration of exchangeable Ca. For the acidic forest topsoils (pH < 5), the stability of OM(PY) was found to increase as the pH, and the concentration of C=O groups and Na-pyrophosphate soluble Mg increase. Y1 - 2012 U6 - https://doi.org/10.1029/2011JG001712 SN - 0148-0227 VL - 117 IS - 4 PB - American Geophysical Union CY - Washington ER - TY - JOUR A1 - Kaiser, Michael A1 - Ellerbrock, Ruth H. A1 - Sommer, Michael T1 - Separation of coarse organic particles from bulk surface soil samples by electrostatic attraction N2 - Different separation procedures are suggested for studying the stability and functionality of sod organic matter (OM). Density fractionation procedures using high-molarity, water-based salt solutions to separate organic particles may cause losses or transfers of C between particle and soluble OM fractions during separation, which may be a result of solution processes. The objective of this study was to separate coarse organic particles (>0.315 mm) from air- dried surface soil samples to avoid such solution processes as far as possible. Air-dried surface soil samples (<2 mm) from nine adjacent arable and forest sites were sieved into five soil particle size fractions (2-1.25, 1.25-0.8, 0.8- 0.5, 0.5-0.4, and 0.4-0.315 mm). Coarse organic particles were separated from each of these fractions using electrostatic attraction by a charged glass surface. The sum of the total dry matter content of the electrostatically separated coarse organic particles ranged from 0.05 to 140 g kg(-1). Scanning electron microscopy images and organic C (OC) analyses indicated, however, that the coarse organic particle fractions were also composed of 20 to 76% mineral particles (i.e., 200-760 g mineral kg(-1) fraction). The repeatability of the electrostatic attraction procedure falls within a range similar to that of accepted density fractionation methods using high-molarity salt solutions. Based on the similarity in repeatability, we suggest that the electrostatic attraction procedure will successfully remove coarse organic particles (>0.315 mm) from air-dried surface soil samples. Because aqueous solutions are not used, the electrostatic attraction procedure to separate coarse organic particles avoids C losses and transfers associated with solution-dependent techniques. Therefore, this method can be used as a pretreatment for subsequent density- or solubility-based soil OM fractionation procedures. Y1 - 2009 UR - https://www.soils.org/publications/sssaj U6 - https://doi.org/10.2136/sssaj2009.0046 SN - 0361-5995 ER -