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  • Springer (CrossRef)  (17)
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  • 1
    Language: English
    In: Plant and Soil, 2013, Vol.370(1), pp.497-509
    Description: Aims: We analysed current carbon (C) stocks in fine root and aboveground biomass of riparian forests and influential environmental parameters on either side of a dike in the Donau-Auen National Park, Austria. Methods: On both sides of the dike, carbon (C) stock of fine roots (CFR) under four dominant tree species and of aboveground biomass (CAB) were assessed by topsoil cores (0-30 cm) and angle count sampling method respectively (n=48). C stocks were modeled, performing boosted regression trees (BRT). Results: Overall CFR was 2.8 t ha super(-1), with significantly higher C stocks in diked (DRF) compared to flooded riparian forests (FRF). In contrast to CFR, mean CAB was 123 t ha super(-1) and lower in DRF compared to FRF. However, dike construction was consistently ruled out as a predictor variable in BRT. CFR was influenced by the distance to the Danube River and the dominant tree species. CAB was mainly influenced by the magnitude of fluctuations in the groundwater table and the distances to the river and the low groundwater table. Conclusions: Despite pronounced differences in FRF and DRF, we conclude that there is only weak support that dikes directly influence C allocation in floodplain forests within the time scale considered (110 years).
    Keywords: Aboveground biomass ; Belowground biomass ; Carbon distribution ; Carbon sequestration ; Dike ; Ecosystem services ; Floodplain forest
    ISSN: 0032-079X
    E-ISSN: 1573-5036
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  • 2
    Language: English
    In: Nutrient Cycling in Agroecosystems, 2012, Vol.93(1), pp.75-88
    Description: Topsoil constituents are eroded from agricultural sites and leached towards drainage channels. This transfer can affect aquatic ecosystems and deteriorate the efficiency of drainage systems and fertilisers. As long as erosion cannot be completely avoided, the recycling of sediments and associated nutrients may offer a sustainable solution to these problems. The aim of our case study at the island Sant Erasmo, lagoon of Venice (Italy) was to assess the ecological problems and potentials of sediment recycling. With our assessment we concentrated on (1) the origin of channel sediments, (2) the benefit of sediment application for increasing the nutrient stocks of the soils, and (3) the risk of heavy metal (HM) contamination of arable soils by sediment application. Samples from soils of horticultural sites, sediments, and waters from adjacent drainage channels and lagoon sediments were analyzed for the concentrations of nutrients (P and K) and HM (Cu, Pb, and Zn). Potentially available channel sediment masses and element stocks were calculated for the soil fertility classes of Sant Erasmo based on local measurements of sediment depths and analyses of aerial photographs by a geographic information system. In a column experiment, leaching of both nutrients and Cu from recently dredged sediments was analyzed. Heavy metal concentrations of soils and channel sediments were much higher than of lagoon sediments. The similarity of the chemical properties of the channel sediments and of top soil samples implies that topsoil material is eroded into the channels. The amount of sediments accumulated in the channels corresponded to soil erosion rates between 2 and 23 t ha −1  a −1 . Channel sediments contained higher concentrations of nutrients and organic carbon but slightly lower concentrations of HM than the soils of adjacent horticultural sites. Sediment P and K yields would be sufficient to replace fertiliser application at the horticultural sites for up to 51 and 35 years, respectively. The column experiment indicated that Cu mobilization induced by oxidation processes is restricted to the first years after sediments are applied to the soils. Our study emphasizes that for a comprehensive assessment of sediment recycling in agricultural systems the available sediment stocks as well as the contents of nutrients and pollutants of the sediment in relation to soils have to be considered.
    Keywords: Phosphorus ; Heavy metals ; Nutrient cycling ; Leaching experiment
    ISSN: 1385-1314
    E-ISSN: 1573-0867
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  • 3
    Language: English
    In: Journal of Soils and Sediments, 2013, Vol.13(3), pp.606-615
    Description: Byline: Horst Schonsky (1), Andre Peters (1), Friederike Lang (2), Stefan Abel (1), Beate Mekiffer (3), Gerd Wessolek (1) Keywords: Column experiment; Construction rubble; Numerical modeling; Sulfate; Urban soil Abstract: Purpose In Berlin and many other cities, technogenic soil substrates from World War II and building and construction debris, in general, play an important role for soil formation and solute transport in the vadose zone. The largest debris landfill in Berlin is the Teufelsberg. Sulfate release from the landfill poses threats to groundwater quality. The scope of this study is to determine and model the processes controlling sulfate release from soils containing construction rubble. Materials and methods Column leaching experiments were conducted to analyze sulfate mobilization from Teufelsberg topsoil material. Flow interruptions of 1 and 7 days were applied. Sulfate release was modeled using a geochemical simulation tool (HP1). The model considered water flux, solute transport, and precipitation/dissolution with first-order kinetics. Results and discussion Sulfate release increased after flow interruptions, although bromide breakthrough indicated physical equilibrium of transport processes. Hence, kinetically limited solution/dissolution of sulfate is assumed. The model was applicable for qualitative description of our experimental results. The estimated equilibrium concentrations of sulfate were one to two orders of magnitude smaller than expected according to the equilibrium constant of gypsum. Conclusions It is assumed that the mobilization and transport of sulfate from debris soil material can be described by an effective model. If sulfate release and transport from soils containing debris is modeled using literature values of thermodynamic constants for gypsum, sulfate concentrations will be overestimated by one to two orders of magnitude. Author Affiliation: (1) Fachgebiet Standortkunde und Bodenschutz, Technische Universitat Berlin, Ernst Reuter Platz 1, 10587, Berlin, Germany (2) Institut fur Bodenkunde und Waldernahrungslehre, Albert Ludwig Universitat Freiburg, Bertoldstr. 17, 79085, Freiburg i.Br., Germany (3) WISTA-MANAGEMENT GMBH, Rudower Chaussee 17, 12489, Berlin, Germany Article History: Registration Date: 01/10/2012 Received Date: 12/12/2011 Accepted Date: 01/10/2012 Online Date: 19/10/2012 Article note: Responsible editor: Jean Louis Morel
    Keywords: Column experiment ; Construction rubble ; Numerical modeling ; Sulfate ; Urban soil
    ISSN: 1439-0108
    E-ISSN: 1614-7480
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  • 4
    Language: English
    In: Plant and Soil, 2005, Vol.275(1), pp.vii-vii
    Description: Issue Title: Kinetics of soil physico - chemical processes
    Keywords: Life Sciences ; Plant Sciences ; Ecology ; Plant Physiology ; Soil Science & Conservation ; Agriculture ; Botany ; Ecology;
    ISSN: 0032-079X
    E-ISSN: 1573-5036
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  • 5
    Language: English
    In: Journal of Soils and Sediments, 2015, Vol.15(1), pp.1-12
    Description: Byline: Daniela Gildemeister (1,2), George Metreveli (1), Sandra Spielvogel (3), Sabina Hens (1,4), Friederike Lang (5), Gabriele E. Schaumann (1) Keywords: Cation bridges; Cross-link; Differential scanning calorimetry; Dissolved organic matter; Glass transition; Water molecule bridges Abstract: Purpose Precipitation of dissolved organic matter (DOM) by multivalent cations is important for biogeochemical cycling of organic carbon. We investigated to which extent cation bridges are involved in DOM precipitation and how cross-links by cations and water molecule bridges (WaMB) stabilise the matrix of precipitated DOM. Materials and methods DOM was precipitated from the aqueous extract of a forest floor layer adding solutions of Ca(NO.sub.3).sub.2, Al(NO.sub.3).sub.3 and Pb(NO.sub.3).sub.2 with different initial metal cation/C (Me/C) ratios. Precipitates were investigated by differential scanning calorimetry before and after ageing to detect cation bridges, WaMB and restructuring of supramolecular structure. Results and discussion Twenty-five to sixty-seven per cent of the dissolved organic carbon was precipitated. The precipitation efficiency of cations increased in the order Ca〈Al〈Pb, while the cation content of precipitates increased in the order Pb〈Ca〈Al. The different order and the decrease in the WaMB transition temperature (T*) for Al/C〉3 is explained by additional formation of small AlOOH particles. Thermal analysis indicated WaMB and their disruption at T* of 53--65 [degrees]C. Like cation content, T* increased with increasing Me/C ratio and in the order Ca〈Pb〈Al for low Me/C. This supports the general assumption that cross-linking ability increases in the order Ca〈Pb〈Al. The low T* for high initial Me/C suggests less stable and less cross-linked precipitates than for low Me/C ratios. Conclusions Our results suggest a very similar thermal behaviour of OM bound in precipitates compared with soil organic matter and confirms the relevance of WaMB in stabilisation of the supramolecular structure of cation-DOM precipitates. Thus, stabilisation of the supramolecular structure of the DOM precipitates is subjected to dynamics in soils. Author Affiliation: (1) Institute for Environmental Sciences, Group of Environmental and Soil Chemistry, Universitat Koblenz-Landau, Fortstr. 7, 76829, Landau, Germany (2) Umweltbundesamt, FG IV 2.2 Pharmaceuticals, Worlitzer Platz 1, 06844, Dessau-Ro[sz]lau, Germany (3) Department of Geography, Institute of Integrated Natural Sciences, Universitat Koblenz-Landau, Universitatsstr. 1, 56070, Koblenz, Germany (4) GN Dr. Netta Beratende Ingenieure und Geowissenschaftler, Bienengarten 3, 56072, Koblenz, Germany (5) Albert-Ludwigs-Universitat Freiburg, Institute of Forest Sciences, 79085, Freiburg i.Br., Germany Article History: Registration Date: 09/07/2014 Received Date: 02/04/2014 Accepted Date: 09/07/2014 Online Date: 30/07/2014 Article note: Responsible editor: Dong-Mei Zhou Electronic supplementary material The online version of this article (doi: 10.1007/s11368-014-0946-9) contains supplementary material, which is available to authorized users.
    Keywords: Cation bridges ; Cross-link ; Differential scanning calorimetry ; Dissolved organic matter ; Glass transition ; Water molecule bridges
    ISSN: 1439-0108
    E-ISSN: 1614-7480
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  • 6
    Language: English
    In: Plant and Soil, 2018, Vol.432(1), pp.289-301
    Description: Aims The accumulation of organic layers in forests is linked to decreasing nutrient availability. Organic layers might represent a source of phosphorus (P) nutrition of trees in forests. Our aims were i) to test if the fate of P in a tree sapling-soil system differs between nutrient-poor and nutrient-rich sites, and ii) to assess the influence of organic layers on the fate of P in a tree sapling-soil system at either site. Methods We conducted a 33P labeling experiment of mesocosms of beech (Fagus sylvatica) saplings. Results Recovery of 33P in the organic layer was greater under nutrient-poor than under nutrient-rich conditions likely caused by the abundance of microorganisms and roots. Under nutrient-poor conditions, we found that the mobilization of P followed by efficient uptake promoted tree sapling growth if the organic layer was present. The presence of organic layers did not significantly influence P uptake by beech saplings under nutrient-rich conditions suggesting mechanisms of P mobilization in addition to organic matter mineralization. Conclusions Our results highlight the importance of organic layers for P nutrition of young beech trees growing on nutrient-poor soils in temperate forest ecosystems. The role of organic layers should be considered for sustainable forest management.
    Keywords: P tracer ; Phosphorus nutrition ; Forest floor ; Soil ; Beech ; Phosphorus uptake
    ISSN: 0032-079X
    E-ISSN: 1573-5036
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  • 7
    Language: English
    In: Plant and Soil, 2018, Vol.427(1), pp.53-69
    Description: Background and aims Phosphorus (P) availability is crucial for forest ecosystem productivity and soil organic matter (SOM) is an important source for P. This study was conducted to reveal carbon (C), nitrogen (N) and P distributions in functional SOM fractions. We hypothesised that (1) most of the organic P (P.sub.org) is part of the particulate SOM, (2) particulate SOM stores increasing share of P with decreasing soil P content and (3) the C:P.sub.org ratio of mineral-associated SOM is smaller than that of particulate SOM. Methods We analysed soil samples from five temperate forest sites (Fagus sylvatica) under different geological parent material with a wide range of total P concentrations. Density fractionation was used to separate free light fraction (fLF), particulate SOM occluded within soil aggregates (occluded light fraction; oLF), and mineral associated SOM (heavy fraction; HF). We determined the mass balance of P in these fractions, in addition to the C and N concentrations. Additionally, the P speciation of the topsoil was analysed by X-ray absorption near edge structure (XANES) spectroscopy at the P K-edge. Results The fLF contained 18-54% and the oLF 1-15% of total P (P.sub.tot). High percentage of P in these light fractions was associated to soil minerals. Phosphorous in particulate SOM within aggregates tend to increase with decreasing soil P. The HF containing mineral-associated OM, comprised 38-71% of P.sub.tot and their C:P.sub.org ratios were consistently lower than those of the fLF irrespective of the P status of the soil. Conclusions We show that all three functional SOM fractions contain variable amount of both organic and inorganic P species. The free light fraction shows no response to changing P stocks of soils.. Despite physically protected particulate SOM, oLF, becomes increasingly relevant as P cache in soils with declining P status.
    Keywords: Ecosystem nutrition ; Density fractions ; Soil organic matter ; C:N:P ratio ; Phosphorus ; P K-edge XANES
    ISSN: 0032-079X
    E-ISSN: 1573-5036
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  • 8
    Language: English
    In: Plant and Soil, 2018, Vol.427(1), pp.71-86
    Description: Background and aims Nanoparticles and colloids affect the mobilisation and availability of phosphorus for plants and microorganisms in soils. We aimed to give a description of colloid sizes and composition from forest soil profiles and to evaluate the size-related quality of colloids for P fixation. Methods We investigated the size-dependent elemental composition and the P content of water-dispersible colloids (WDC) isolated from five German (beech-dominated) forest soil profiles of varying bulk soil P content by field-flow fractionation (FFF) coupled to various detectors. Results Three size fractions of WDC were separated: (i) nanoparticles 25 nm (NP) rich in C.sub.org, (ii) fine colloids (25 nm-240 nm; FC) composed mainly of C.sub.org, Fe and Al, probably as associations of Fe- and Al- (hydr)oxides and organic matter, and (iii) medium-sized colloids (240 nm-500 nm; MC), rich in Fe, Al and Si, indicating the presence of phyllosilicates. The P concentration in the overall WDC was up to 16 times higher compared to the bulk soil. The NP content decreased with increasing soil depth while the FC and MC showed a local maximum in the mineral topsoil due to soil acidification, although variant distributions in the subsoil were observed. NP were of great relevance for P binding in the organic surface layers, whereas FC- and MC-associated P dominated in the Ah horizon. Conclusion The nanoparticles and colloids appeared to be of high relevance as P carriers in the forest surface soils studied, regardless of the bulk soil P content.
    Keywords: Colloids ; Field-flow fractionation ; Forest soil ; Nanoparticles ; Phosphorus
    ISSN: 0032-079X
    E-ISSN: 1573-5036
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  • 9
    Language: English
    In: Journal of Soils and Sediments, 2012, Vol.12(8), pp.1209-1210
    Description: Issue Title: Special issue: Coevolution of organic substances and soils
    Keywords: Environment ; Environmental Physics ; Soil Science & Conservation ; Environment, General ; Agriculture;
    ISSN: 1439-0108
    E-ISSN: 1614-7480
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  • 10
    Language: English
    In: Journal of Thermal Analysis and Calorimetry, 2014, Vol.118(2), pp.1203-1213
    Description: Multivalent cations are suggested to influence the supramolecular structure of soil organic matter (SOM) via inter- and intra-molecular interactions with SOM functional groups. In this study, we tested the combined effect of cations, temperature treatment, and isothermal aging on SOM matrix properties. Samples from a peat and a mineral soil were either enriched with Na, Ca, and Al or desalinated in batch experiments. After treatment at 25, 40, 60, and 105 °C and after different periods of aging at 19 °C and 31 % relative humidity, we investigated the physicochemical matrix stability and the thermal stability against combustion. We hypothesized that multivalent cations stabilize the SOM matrix, that these structures disrupt at elevated temperatures, and that aging leads to an increase in matrix stability. The results show that cation-specific effects on matrix rigidity started to evolve in the peat only after 8 weeks of aging and were significantly lower than the temperature effects. Temperature treatment above 40 °C caused a non (or not immediately) reversible loss of water molecule bridges (WaMB) and above 60 °C a partly reversible melting process probably of semi-crystalline poly(methylene). Thermal stability increased with increasing cation valence and degree of protonation and was much less affected by temperature. Generally, Na-treated and control samples revealed lower thermal stability and lower increase in matrix rigidity with aging than those treated with Ca, Al, and H. We conclude that drying at elevated temperatures (〉40 °C) may irreversibly change SOM structure via disruption of labile cross-links and melting of semi-crystalline domains.
    Keywords: Cation ; Combustion enthalpy ; Differential scanning calorimetry (DSC) ; Soil organic matter (SOM) ; Step transition
    ISSN: 1388-6150
    E-ISSN: 1588-2926
    E-ISSN: 15728943
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