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1.
‘Colluvisols’ (Colluvi-cumulic Anthrosols) are an important soil unit in North Germany. In the landscape of loamy till these soils are associated with eroded Luvisols. The soil organic matter (SOM) of top layers of both soils was compared by using approaches of wet chemistry, CPMAS 13C-NMR and pyrolysis field-ionization mass spectrometry (Py-FIMS). The Luvisols are sources of SOM transfer due to a continuous erosion process. The annual input of straw and plant residues induces the dominance of litter compounds like proteins, polysaccharides and lignin in the SOM. The Colluvisols are sinks of SOM transfer with a predominance of humic compounds. Lignin is degraded forming humic compounds with an alkylic and aromatic structure. In these soils selected compounds with higher mass signals were detected by Py-FIMS, which may indicate the existence of typical “SOM markers” in the colluvic materials.  相似文献   

2.
We studied quantitative and qualitative changes in soil organic matter (SOM) due to different land uses (reference woodland versus cultivated) on six soils from Tanzania (Mkindo and Mafiga), Zimbabwe (Domboshawa and Chickwaka), and South Africa (Hertzog and Guquka). Structural characteristics of the humic acids (HAs) were measured by Curie-point pyrolysis–gas chromatography/mass spectrometry (Py–GC/MS) and solid-state 13C nuclear magnetic resonance (CPMAS 13C NMR) spectroscopy. Significant changes in concentration and composition of SOM were observed between land uses. Losses of organic carbon after cultivation ranged from 35% to 50%. Virgin soils showed large proportions of colloidal humus fractions: humic acids (HAs) and fulvic acids (FAs) but negligible amounts of not-yet decomposed organic residues. The change in land use produced a contrasting effect on the composition of the HAs: a noteworthy “alkyl enhancement” in Mkindo soil and “alkyl depletion” in Chikwaka and to a lesser extent in Domwoshawa. The remaining soils displayed only minor alterations.  相似文献   

3.
The composition of soil organic matter (SOM) on sewage farms south of Berlin was investigated by solid-state CP/MAS 13C-NMR and pyrolysis-field ionization mass spectrometry (Py-FIMS) of freeze-dried sewage solids and soil samples of differing contamination. These were an untreated soil (USOIL), a former sewage farm used as arable land since 1990 (SF90A), and a recent sewage farm (SF1994). The CP/MAS 13C-NMR spectra showed enrichments of the sewage-treated soils with aliphatic C and C in OCH3-groups and amino acids. In the Py-FI mass spectra the major markers of sewage and SOM in sewage farm soils were (i) N-containing compounds, in particular peptides, (ii) dimethylphthalate (m/z 194), (iii) sterols, and (iv) signals in the mass range m/z 502 to 554 of mono- and diaryl esters which were substituted by long aliphatic chains. The latter signals were intense in the sewage solids, increased in intensity from sample SF90A to SF1994; but they were not present in the USOIL, thus clearly indicating anthropogenic origin. Temperature-resolved Py-FIMS showed that the SOM compounds in the sewage farm soils were generally incorporated into bonds with widely different stabilities which could be relevant for SOM turnover and environmental effects. This is demonstrated for the trapping of dimethylphthalate in a modelled humic substance.  相似文献   

4.
Conversion of natural forest to agricultural land use has significantly lowered the soil organic matter (SOM) content in sandy soils of northeast Thailand. This paper reviews the findings of comparative studies on contents of SOM pools (labile, i.e. microbial biomass and particulate organic matter—POM and stable, i.e. humic substance) and related soil aggregate formation, in natural forest plots and cultivated fields (monocrops of cassava, sugarcane and rice) in sites representative of northeast Thailand from the viewpoints of terrain (i.e. undulating), soils (sandy) and land use and discusses the restoration of SOM and fertility (nitrogen) in these degraded soils. Monocultural agriculture brings about the degradation of all SOM pools and associated soil aggregation as compared to the forest system because of decreased organic inputs and more frequent soil disturbance. The build‐up of SOM was achieved through the continuous recycling of organic residues produced within the system. Low‐quality residues contributed the largest SOM build‐up in whole and fractionated SOM pools, including POM and humic substance. However, to restore N fertility, high quality residues, (i.e. with low C/N ratios, lignin and polyphenols) were also needed. Timing of N release to meet crop demand was achieved by employing a mixture of high and low quality residues. Selection of appropriate residues for N sources was affected by environmental factors, notably soil moisture regimes, which differed in upland field and lowland paddy subsystems. Copyright © 2007 John Wiley & Sons, Ltd.  相似文献   

5.
Abstract

Knowledge of the distribution of soil organic matter (SOM) fractions is important in managing soils toward a sustainable agricultural system in a tropical environment. However, data on Histosols is limited. This study developed 19 profiles of Histosols and soils with high organic-matter content from different regions of Brazil. Soil organic matter was fractionated into fulvic acids (FAF), humic acids (HAF), and humin (HUM). The ratios HAF/FAF and AE (alkaline extract)/HUM were calculated. The objectives were to evaluate the method for SOM fractionating in Histosols and related soils and to correlate the distribution of organic fractions with other soil attributes. The humic fractions presented significant correlations with other soil attributes, the best being the correlation between FAF and nutrient level. The HAF and HUM presented high correlation with cationic exchange capacity, active acidity (H+) and pH. Humin and the alkaline extract absorbance measured at 380 nm and 465 nm and presented good correlation with total organic carbon.  相似文献   

6.
Two arable soils and one pasture soil had previously been air-dried for 6 d and stored at room temperature. The enzyme activities remaining after this treatment were constant. The soils were then extracted with 140 mM sodium pyrophosphate at pH 7.1. Amino acid N and total organic C content of soils and soil extracts, together with humic and fulvic acids content of soil extracts were determined. Total organic C was determined in soil residues obtained after extraction. Chemical characterization of the organic matter of soils, soil extracts and soil residues was carried out by pyrolysis–gas chromatography (Py–GC). Protease activity was determined in soil extracts and soil residues by using three different substrates: N-benzoyl- -argininamide (BAA), specific for trypsin; N-benzyloxycarbonyl- -phenylalanyl -leucine (ZPL), specific for carboxypeptidases, and casein, essentially non-specific. Comparative studies between specific activities referred to organic C in soils, soil extracts and soil residues and their corresponding pyrogram composition, and also between total extracted or residual activity and the humine or unhumified organic matter content of the corresponding soil, allowed us to establish hypotheses about the type of organic matter the enzymes are associated with. From 12% to 21% of the soil organic C (33% to 39% of which were humic acids) and from 3% and 18% of amino acid N were extracted from soil using pyrophosphate. Py–GC analyses showed that pyrophosphate was effective in extracting condensed humic substances and glycoproteins and that the organic matter present in soil extracts was especially rich in intact or partially-decomposed fresh residues of carbohydrate origin and also in certain humus-associated proteins. Extracted BAA-hydrolysing activity accounted for 11% to 36% of the soil activity, depending on soil type. Extracted ZPL- and casein-hydrolysing activities were, with one exception, remarkably high, accounting for about 100% or even more of the soil activity, depending on soil type. According to the results BAA-hydrolysing proteases are probably mostly associated with highly condensed humus, ZPL-hydrolysing proteases with less condensed humic substances and casein-hydrolysing proteases with fresh organic matter.  相似文献   

7.
珠江三角洲地区土壤与表层沉积物有机质的性质结构研究   总被引：11，自引：1，他引：11  
通过分析海洋、河流、池塘和稻田四种热带 /亚热带土壤与表层沉积物及用化学方法分离的有机质 ,证明了土壤与沉积物有机质是高度不均匀的 ,除了包括腐殖酸和演化程度较深的干酪根外 ,强调了演化程度更深的碳黑的存在 ,并对不同有机质的来源、性质和结构进行了表征。腐殖酸和干酪根来源于生物体的演化 ,在结构上后者比前者致密 ;碳黑来源于化石燃料和生物体的不完全燃烧 ,具有更致密的结构 ,对有机质的非均质性影响很大。因此可认为 ,系统地研究土壤与表层沉积物有机质的非均质性及组分特征对了解地球表层的生物地球化学过程和疏水性毒害有机污染物在环境中的迁移具有重要的意义。  相似文献   

8.
Montane volcanic ash soils contain disproportionate amounts of soil organic carbon and thereby play an often underestimated role in the global carbon cycle.Given the central role of Al and Fe in stabilizing organic matter in volcanic ash soils,we assessed various extraction methods of Al,Fe,and C fractions from montane volcanic ash soils in northern Ecuador,aiming at elucidating the role of Al and Fe in stabilizing soil organic matter(SOM).We found extractions with cold sodium hydroxide,ammonium oxalate/oxalic acid,sodium pyrophosphate,and sodium tetraborate to be particularly useful.Combination of these methods yielded information about the role of the mineral phase in stabilizing organic matter and the differences in type and degree of complexation of organic matter with Al and Fe in the various horizons and soil profiles.Sodium tetraborate extraction proved the only soft extraction method that yielded simultaneous information about the Al,Fe,and C fractions extracted.It also appeared to differentiate between SOM fractions of different stability.The fractions of copper chloride-and potassium chloride-extractable Al were useful in assessing the total reactive and toxic Al fractions,respectively.The classical subdivision of organic matter into humic acids,fulvic acids,and humin added little useful information.The use of fulvic acids as a proxy for mobile organic matter as done in several model-based approaches seems invalid in the soils studied.  相似文献   

9.
东北黑土有机质组分与结构的研究进展   总被引：11，自引：1，他引：10  
梁尧  韩晓增  丁雪丽 《土壤》2012,44(6):888-897
在全球气候变化背景下研究土壤有机质的转化过程对于评价陆地生态系统碳截获潜力具有重要意义,而土壤有机质的循环特征及其稳定性与土壤有机质的组成和结构密切相关.东北黑土区是我国重要的商品粮基地,近年来,黑土有机质含量呈显著下降趋势,造成黑土肥力和质量的严重退化.本文通过文献资料的整理,总结了不同农田管理措施下黑土土壤有机质的消长动态、组分变化以及结构特征的研究现状,并探讨了研究中存在的问题.开垦和耕作导致土壤有机质总量、活性组分以及腐殖物质含量的显著降低,而平衡施用化肥和有机肥是维持和提升土壤有机质数量和质量的有效途径,长期有机无机配施使土壤有机质结构趋于简单化,有利于土壤肥力的保持.黑土有机质组分化学结构变化的驱动机制是值得人们长期探索的问题.  相似文献   

10.
Abstract

A neutral phosphate buffer (NPB) extraction method has been used to estimate the amount of available N in soil. However, the properties of soil NPB-extractable organic N have not been fully elucidated. The purpose of the present study was to characterize the properties of organic matter in the NPB extracts of soils. The NPB extracts were obtained from three soil samples, and the organic matter in the extracts was separated into three fractions according to its solubility in acid and adsorption onto polyvinylpyrrolidone (PVP). High-performance size exclusion chromatography (HPSEC) with ultraviolet (UV) and fluorescence detections was applied to the NPB extracts and their fractions. The HPSEC analysis of the NPB extract revealed the presence of a single broad peak, irrespective of the detection methods. The broad peak was identified as humic substances using the on-flow measurements of UV absorption spectra and fluorescence emission spectra. Among the fractions, the PVP-non-adsorbed fulvic acid (FA) fraction accounted for the largest proportion of organic C or N in the NPB extract, followed by the PVP-adsorbed FA and humic acid (HA) fractions. The peak of humic substances was observed for all fractions using HPSEC with the on-flow measurement of UV absorption and fluorescence emission spectra. The molecular weight of the humic substances varied with each fraction. When the Coomassie Blue-reactive substances (CBRS) were quantified using a Bradford protein assay, they were detected in the NPB extract and almost half were distributed in the PVP-non-adsorbed FA fraction. However, humic substances were considered to be the main constituents of CBRS in the soil NPB extract because of their reactivity with Coomassie Blue and the absence of proteinaceous materials. Furthermore, an incubation experiment revealed that the organic matter available to microorganisms was included in the HA and PVP-non-adsorbed FA fractions. Based on the HPSEC analysis of the NPB extracts and their fractions, it was observed that the humic substances in the NPB extract, particularly in the HA and PVP-non-adsorbed FA fractions, were available to microorganisms.  相似文献   

11.
The chemical identity of organic nitrogen (N) containing compounds in soils is only partially known, because 20—35% of soil N can not be hydrolyzed and identified by wet‐chemical methods. Therefore a new methodology for investigations of the extractability and composition of nonhydrolyzed N was developed using a combination of selective extraction, wet‐chemical analyses and pyrolysis‐mass spectrometry. Residues of organic matter hydrolysis with 6 M HCl from particle‐size separates and whole soils of five sites in Thyrow, 2 × Halle, Lauterbach and Bad Lauchstädt (Germany) were treated with dithionite/citrate/bicarbonate (DCB) to remove pedogenic oxides and bound N‐containing compounds. Between 13 and 61% (mean 34 ± 13%) of nonhydrolyzed N (Nnhydr) was extracted with DCB. For all particle‐size separates, there was a close positive correlation between the contents of nonhydrolyzed N and DCB extractable Al and Fe, respectively. Univariate analysis of variance and Pearson correlation coefficients showed that the specific surface areas of samples were the major factor determining the contents of Nnhydr. About 30—50% of the variation in Nnhydr could be explained by the variation in the contents of pedogenic oxides. In the DCB extraction residues an additional portion of 12 to 66% of N was hydrolyzed by 6 M HCl. About 75% of total N in the DCB extracts was hydrolyzed, and 29% was identified as α‐amino‐N. Amino acid analysis showed that the DCB extracts from clay and fine silt contained all amino acids characteristic of soils. Pyrolysis‐field ionization mass spectrometry (Py‐FIMS) of a freeze‐dried DCB extract indicated the presence of peptides (about 5% of total ion intensity) and heterocyclic N‐containing compounds (about 3% of total ion intensity). In summary, these results provide evidence that organic‐mineral bonds at reactive surfaces (silicates, pedogenic oxides, alkali‐extractable organic substances) are the main factors for the nonhydrolyzability of significant amounts of organic N, including peptides. It is concluded that the processes of trapping and binding of proteinaceous compounds proceed as postulated for recent models of soil organic matter (SOM) and soil particles. Molecular mechanics calculations show large gaps between SOM and the mineral matrix and as well as fine pores and voids in SOM which have a strong potential to occlude and bind peptides (hydrogen bonds).  相似文献   

12.
《Geoderma》2006,130(1-2):141-156
Sixteen Orthic Chernozemic surface soil samples, one half from virgin prairie and one half from adjacent cultivated prairie (cultivated for 31 to 94 years), were collected from eight sites throughout Southern Saskatchewan, Canada. Samples were analyzed for total organic C and a number of other chemical and physical properties. The virgin and cultivated soils at site No. 4 were selected for more detailed analysis by CP-MAS 13C NMR, Curie-point-pyrolysis-gas chromatography/mass spectrometry (Cp-Py-GC/MS), and by pyrolysis-field ionization mass spectrometry (Py-FIMS). Long-term cultivation resulted in large significant decreases in total SOM (soil organic matter), as represented by total soil organic C. There were significant increases in aromaticity of the SOM as a result of long-term cultivation as indicated by CP-MAS 13C NMR spectroscopy. This was mainly attributable to the result of cultivation-enhanced degradation of aliphatic C relative to aromatic C. Organic compounds identified in the Cp-Py-GC/MS spectra of the virgin and cultivated soils at site No. 4 consisted of n-alkanes (ranging from C11 to C22) and alkenes (ranging from C7:1 to C21:1), with the virgin soil being richer in alkenes than the cultivated soil. Other components identified were cyclic aromatics, carbocyclics, N-containing aromatics, N-heterocyclics, benzene and substituted benzenes, phenols and substituted phenols and substituted furans. The compounds identified appeared to originate from long-chain aliphatics, lignins, polyphenols, aromatics, polysaccharides, and N-containing compounds in the two soils. While qualitatively similar compounds were identified by Py-FIMS in the two soils, the total ion intensity (TII) of the virgin soil was almost 2.5 times as high as that of the cultivated soil. This suggests that cultivation made the organic matter less volatile, either by favouring the formation of higher molecular weight organic matter or by promoting the formation of non-volatile metal-organic matter complexes. The Py-FIMS spectra showed that the virgin soil contained relatively more lignin dimers, lipids, sterols, and n-C16 to n-C34 fatty acids than the cultivated soil. Thus, conversely, the cultivated soil was richer in carbohydrates, phenols and lignin monomers, alkyl aromatics and N-containing compounds, including peptides, than the virgin soil.  相似文献   

13.
Two types of the natural organic matter P and B were isolated from dried figs by gel permeation and high-performance liquid chromatography. The characterizations of their molecular structures were also performed using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry and infrared absorption spectrometry. As a result, these samples were revealed to inhibit the serine and cysteine proteinases chymotrypsin and papain (K(i) = 10(-)(6)-10(-)(4) M). The optimal inhibitory pH values of the P and B samples were observed to be approximately 5.5 and 5.0, respectively. The analyses of their UV-vis absorption spectra and infrared absorption spectra indicated that they would be a kind of humic substance. The mass spectrometry analyses showed that they possessed relatively small heterogeneous molecules with molecular masses around 692, 845, and 1389 Da for the P sample and around 551, 704, and 909 Da for the B sample.  相似文献   

14.
Abstract

Determinations were made of total soil organic matter (SOM), stable and labile organic fractions, biomass carbon (C), and chemical composition of several humus‐soil‐fractions in Chilean volcanic soils, Andosols and Ultisols. Their physico‐chemical properties and humification degree at different stages in edaphic evolution were also assessed. In addition, organic matter models were obtained by chemical and biological syntheses and the structures and properties of natural and synthetic humic materials were compared with SOM. Results indicate that Andosols have higher SOM levels than Ultisols, but the fraction distribution in the latter suggests a shift of the more stable fractions to the more labile ones. Moreover, contents of humines, and humic and fulvic acids suggest that Chilean volcanic soil SOM is highly humified. On the other hand, among the SOM labile fractions, carbohydrate and biomass are about 15% of the SOM which are one of the most important fractions in soil fertility.  相似文献   

15.
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16.
Non destructive spectroscopic methods such as 13C- and 15N-NMR provide new insights into the structure of humic substances. Solid state NMR is capable of studying complete native soils by the CPMAS-technique. By means of nitrogen 15-enriched composts it is suggested that nitrogen in soil organic matter is mainly located in amide and peptide structures. Most probable assignments are given. The investigation of humification processes in forest soils is possible via an approach which uses several fractionation techniques in combination with degradative and non-degradative analytical techniques. Besides structure analysis, the 13C-NMR-spectroscopy provides important information about the functions of humic substances. By using 13C-enriched xenobiotics the binding mechanism to organic matter can be elucidated on a molecular basis. Molecular fluorescence spectrometry, a non-invasive method, is a powerful tool for the quantitative characterization of metal ion complexation by dissolved organic matter in aqueous leaf litter extracts in terms of conditional stability constants and metal binding capacities.  相似文献   

17.
The aim of this paper is to discuss the demand of fresh organic matter (FOM) supply to maintain soil organic matter (SOM) levels and productivity of arable soils under organic management. The basic question is whether the different frame conditions in organic vs. conventional farming result in a different and system‐specific FOM demand. If this is the case, it would follow that the farming system has to be considered in the calculation of SOM balances. SOM balances are the most common decision support tools in organic matter management. A conversion to organic farming in practice usually leads to an increase of SOM levels as well as soil microbial activity over time. The system‐specific driver of this effect is the indispensable extension of the share of (perennial) legumes in crop rotations at the expense of non‐legumes such as cereals, row crops, and maize. Extended legume cropping is essential for N supply in crop rotations as the import of N fertilizer in total is limited by organic farming regulations and mineral N fertilizer may not be used at all. Based on this characteristic of organic management, we argue that the demand of FOM supply to soils must be higher than in conventional crop production. The most relevant factors are (1) the non‐existence of mineral N fertilizer as an external N source that supports the maintenance of SOM by decreasing the demand for SOM‐N, (2) benefits of increasing SOM stocks and turnover for soil productivity under organic management, and, (3) increased mass‐losses of FOM and easily degradable SOM compartments due to higher microbial activity in soils. These effects have to be quantified and must be considered in SOM balances in order to avoid misleading assessments and erroneous decisions.  相似文献   

18.
We used NMR spectroscopy to characterize humid acids extracted from soils that had received long-term application of 2 levels of biosolids to evaluate the soil organic matter (SOM) stability in biosolids-amended soils. The study also quantified fulvic acids (FAs), humic acids (HAs) and Fe/Al oxides. The soils were collected in 2004 from 7 fields, in Fulton County, southwestern Illinois, which received biosolids at a cumulative rate of 0 (control), 554 (low biosolids) and 1,066 (high biosolids) Mg ha−1. The application of biosolids increased both FA and HA contents, but biosolids-amended soil and control soil did not differ in FA/HA ratio. Biosolids application had no effect on water-soluble organic carbon content. Biosolids application increased the presence of Fe/Al in the SOM complex and lowered its C/Fe and C/Al ratios. 13C NMR spectra showed increased alkyl C and decreased aromatic C content in soil HAs with the application of biosolids, and the extent of such changes was higher with high than low biosolids treatment. Under biosolids application, the soil HAs’ C structure shifts from O-alkyl-dominant to alkyl-dominant. Biosolids application does not decrease SOM stability but rather increases the stability of soil humic substances.  相似文献   

19.
Ingrid Kgel-Knabner 《Geoderma》1997,80(3-4):243-270
Nuclear magnetic resonance (NMR) is a valuable tool for the characterization of soil organic matter and humification processes in soils. This review highlights soil organic matter studies based mainly on solid-state 13C and 15N NMR spectroscopy and some emerging applications, that may provide significant progress in our knowledge on soil organic matter. A major advantage of Nmr spectroscopy is that it can be used as a non-invasive method for solid soil samples or soil fractions. Although resolution is limited, one can obtain an overview on the organic matter structures present in the soil sample. Application of 13C and 15N NMR to soils has, for a long time, been confined to the study of bulk soils or humic extracts for structural characterization. The transformations of soil organic C and N are now being investigated after addition of 13C- and 15N-labelled parent materials to the soil and following their evolution in different C and N pools. With labelling techniques it is also possible to study the interaction of organic pollutants with soil organic matter. Contamination of a soil with man-made additives, such as soot or brown coal dust, can also be detected in soils or individual soil fractions.  相似文献   

20.
Soil organic matter (SOM) has long been recognized as an important indicator of soil productivity. The SOM refers to the organic fraction of the soil exclusive of undecayed plant and animal residues. It plays a crucial role in maintaining sustainability of cropping systems by improving soil physical (texture, structure, bulk density, and water-holding capacity), chemical (nutrient availability, cation exchange capacity, reduced aluminum toxicity, and allelopathy), and biological (nitrogen mineralization bacteria, dinitrogen fixation, mycorrhizae fungi, and microbial biomass) properties. The preservation of SOM is crucial to ensure long-term sustainability of agricultural ecosystems. Improvement/preservation of soil organic matter can be achieved by adopting appropriate soil and crop management practices. These practices include conservation tillage, crop rotation, use of organic manures, increasing cropping intensity, use of adequate rate of chemical fertilizers, incorporation of crop residues, liming acidic soils, and keeping land under pasture. Organic matter can adsorb heavy metals in the soils, which reduce toxicity of these metals to plants and reduce their escape to ground water. Similarly, SOM also adsorbs herbicides, which may inhibit contamination of surface and ground water. Furthermore, SOM also functions as a sink to organic carbon and mitigates carbon dioxide (CO2) gas escape to the environment. Globally, soil organic matter contains about three times as much carbon as found in the world's vegetation. Hence, organic matter plays a critical role in the global carbon balance that is thought to be the major factor affecting global warming. Overall, adequate amounts of soil organic matter maintain soil quality, preserve sustainability of cropping systems, and reduce environmental pollution.  相似文献   

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