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1.
In highly weathered tropical conditions, soil organic matter is important for soil quality and productivity. We evaluated the effects of deforestation and subsequent arable cropping on the qualitative and quantitative transformation of the humic pool of the soil at three locations in Nigeria. Cultivation reduced the humic pool in the order: acetone‐soluble hydrophobic fraction (HE) > humic acid (HA) > humin (HU) > fulvic acid (FA), but not to the same degree at all three sites. The C and N contents, as well as the C/N ratios of humic extracts, were large and not substantially influenced by land use. The δ13C values of the humic extracts were invariably more negative in forested soils thereby showing a dilution of δ13C signature with cultivation from C3 to C4 plants. The δ13C values of apolar HE fractions were generally more negative, indicating a reduced sensitivity compared with other humic fractions to turnover of crop residues. The contents of hydrophobic constituents (alkyl and aromatic C), as revealed by cross‐polarization magic angle spinning (CPMAS) 13C‐NMR spectroscopy, in HA, FA and HU were generally < 50%, with the exception of larger hydrophobicity in HU in the forested soil at Nsukka and HA in that at Umudike. The HE fraction contained significantly more apolar constituents, and consequently had a larger intrinsic hydrophobicity than the other humic fractions. The larger reduction of apolar humic constituents than of the less hydrophobic humic fractions, when these soils were deforested for cultivation, indicates that at those sites the stability of accumulated organic matter is to be ascribed mainly to the selective preservation of hydrophobic compounds.  相似文献   

2.
Decomposition and humification were studied within three types of forest humus (mull, moder, and mor) by means of CPMAS 13C NMR spectroscopy combined with degradative methods. The NMR data show that O-alkyl carbon decreases in all soils, and alkyl as well as carboxyl carbon increase as depth and decomposition increase; the percentage of aromatic carbon remains constant at about 25%. With increasing depth the amount of carbon that can be identified as belonging to specific compound classes by wet chemical methods decreases from 60% to 40%. Microbial polysaccharides and the proportion of non polysaccharide O-alkyl carbon increase with depth. A selective preservation of recalcitrant, condensed lignin structural units is also observed. In order to relate the spectroscopic and chemical data from investigations of whole soils with studies of humification, samples were fractionated into fulvic acid, humic acid, and humin fractions. The fulvic acid fraction contains large concentrations of carbohydrates irrespective of the soil horizon. The humic acid fraction contains less polysaccharides, but high amounts of alkyl carbon and aromatic structures. The percentage of aromatic carbon existing in the humic acid fraction increases with depth, probably reflecting the amount and degree of oxidative decomposition of lignin. A loss of methoxyl and phenolic groups is evident in the 13C NMR spectra of the humic acid fraction. The humin fraction resembles relatively unchanged plant-derived materials as evident from the lignin parameters and carbohydrate contents. All the observed data seem to indicate that humic acids originate form oxidative degradation of humin or plant litter.  相似文献   

3.
The dynamics of incorporation of fresh organic residues into the various fractions of soil organic matter have yet to be clarified in terms of chemical structures and mechanisms involved. We studied by 13C‐dilution analysis and CPMAS‐13C‐NMR spectroscopy the distribution of organic carbon from mixed or mulched maize residues into specific defined fractions such as carbohydrates and humic fractions isolated by selective extractants in a year‐long incubation of three European soils. The contents of carbohydrates in soil particle size fractions and relative δ13C values showed no retention of carbohydrates from maize but rather decomposition of those from native organic matter in the soil. By contrast, CPMAS‐13C‐NMR spectra of humic (HA) and fulvic acids (FA) extracted by alkaline solution generally indicated the transfer of maize C (mostly carbohydrates and peptides) into humic materials, whereas spectra of organic matter extracted with an acetone solution (HE) indicated solubilization of an aliphatic‐rich, hydrophobic fraction that seemed not to contain any C from maize. The abundance of 13C showed that all humic fractions behaved as a sink for C from maize residues but the FA fraction was related to the turnover of fresh organic matter more than the HA. Removal of hydrophobic components from incubated soils by acetone solution allowed a subsequent extraction of HA and, especially, FA still containing much C from maize. The combination of isotopic measurements and NMR spectra indicated that while hydrophilic compounds from maize were retained in HA and FA, hydrophobic components in the HE fraction had chemical features similar to those of humin. Our results show that the organic compounds released in soils by mineralization of fresh plant residues are stored mainly in the hydrophilic fraction of humic substances which are, in turn, stabilized against microbial degradation by the most hydrophobic humic matter. Our findings suggest that native soil humic substances contribute to the accumulation of new organic matter in soils.  相似文献   

4.
A combination of solid‐state CPMAS‐13C‐NMR and TMAH thermochemolysis‐GC/MS was applied to investigate the molecular composition of particulate organic matter (POM) separated from a Chinese paddy soil, from the Tai Lake region, under a long‐term field experiment with different fertilizer treatments. The treatments were: (i) no fertilizer application (NF), (ii) chemical fertilizers only (CF), (iii) chemical fertilizer plus pig manure (CFM) and (iv) chemical fertilizer plus crop straw (CFS). CPMAS‐13C‐NMR spectra showed that POM from all treated plots was rich in O‐alkyl‐C compounds, followed by alkyl‐C and aromatic‐C compounds. However, as compared with a control (NF), POM under CFM and CFS treatments exhibited a smaller relative O‐alkyl‐C content and a larger contribution of aromatic‐C and alkyl‐C, thus increasing both aromaticity and hydrophobicity and, hence, recalcitrance of POM samples. Thermochemolysis of POM from all treatments demonstrated a dominance of aliphatic and lignin‐derived compounds. However, the distribution of lignin monomers (p‐hydroxyphenyl, P, guaiacyl, G, and syringyl, S) revealed significant differences among the treatments. The relative distribution of lignin P, G and S monomers in NF, CF and CFS indicated a preferential contribution of annual crops and maize straw, as compared with that found for CFM. Concomitantly, a larger content of aliphatic thermochemolysis derivatives was found for CFS and CFM. The relative increase of aliphatic molecules in CFS was attributed to hydrophobic polyesters from higher plants. In the CF and CFM systems, the presence of aliphatic components of microbial origin suggested a greater microbial activity in comparison with NF and CFS. The combined application of solid state CPMAS‐13C‐NMR and TMAH thermochemolysis‐GC/MS can be used to assess effectively the accumulation of recalcitrant organic compounds in soil POM under long‐term fertilizer application with organic biomass. It is thus inferred that soil organic matter stabilization by molecular recalcitrance contributes to carbon sequestration in Chinese paddy soils under long‐term managements.  相似文献   

5.
Soil organic matter was extracted by a mixture of O.IM Na4P2O: O.IM NaOH from a chronosequence of weakly weathered soils developed on aeolian sand, and fractionated into humin (non-extractable), humic acid, and fulvic acid. The mass of total organic carbon in the profiles, the 14C content and the 13C/12C ratios were also determined. The weight of total carbon increased rapidly at first and then gradually without attaining a steady state. This trend was also shown by the humin and fulvic acid fractions, but the humic acid fraction appeared to have reached a maximum after about 3000 years. The order of total weights of the organic fractions was humin > fulvic acid > humic acid. The evidence suggests that the proportions of the humic fractions formed by decomposition are related to soil differences but not to vegetation. The greater part of the plant material found in the soils appears in the humin and fulvic acid fractions.  相似文献   

6.
This study was conducted to investigate the influence of land-use systems (grassland and cropland) and of long-term no-till cropping systems [bare soil, oat/maize (O/M), pigeon pea+maize (P+M)] on the composition of organic N forms in a subtropical Acrisol. Soil samples collected from the 0- to 2.5-cm layer in the study area (Eldorado do Sul RS, Brazil) were submitted to acid hydrolysis and cross-polarization magic angle spinning (CPMAS) 15N and 13C nuclear magnetic resonance (NMR) spectroscopies. The legume-based cropping system P+M contained the highest contents of non-hydrolysable C and N, hydrolysable C and N, amino acid N and hydrolysed unknown N. The relative proportion of non-hydrolysable N was higher in bare soil (30.0%) and decreased incrementally in other treatments based on the total C and N contents. The amino acid N corresponded to an average of 37.2% of total N, and was not affected by land use and no-till cropping systems. The non-hydrolysable residue contained lower O-alkyl and higher aromatic C concentrations, as revealed by CPMAS 13C NMR spectroscopy, and higher C:N ratio than the bulk soil. No differences in the bulk soil organic matter composition could be detected among treatments, according to CPMAS 13C and 15N NMR spectra. In the non-hydrolysable fraction, grassland showed a lower concentration of aromatic and a higher concentration of alkyl C than other treatments. From CPMAS 15N NMR spectra, it could be concluded that amide N from peptide structures are the main organic N constituent. Amide structures are possibly protected through encapsulation into hydrophobic sites of organic matter and through organomineral interaction.  相似文献   

7.
Humic acids were extracted from the bottom sediment of the three lakes (Zlatari, Vasici and Vodozahvat) that together comprise Lake ?elije a regional drinking water reservoir. The humic acids were examined by high resolution 13C and 1H solution NMR and 13C CPMAS. The aromaticity expressed as the number of benzene rings per 1000 g of humic acid is 1.8 for Zlatari, 2.3 for Vasici and 1.9 for Vodozahvat. Oxygen-substituted aromatic carbon structures in humic acids from the first two lakes (Zlatari and Vasici) are similar and resemble p-coumaryl units in lignin while those in Lake Vodozahvat more closely resemble coniferyl or sinapyl units in lignin. The aromatic rings of all three humic acids are highly substituted. Humic acids from the first two lakes have very similar carbohydrate carbon contents (19.9 and 19.5% respectively) compared to 23.3% for Vodozahvat humic acid. Zlatari and Vodozahvat humic acids have a higher alkyl chain content which indicates a greater potential for forming hydrophobic cavities. The carboxyl and aromatic OH group content of each humic acid influences their capacity for forming complexes with metal ions.  相似文献   

8.

Purpose

Under a global warming scenario, understanding the response of soil organic carbon fractions and aggregate stability to temperature increases is important not only for better understanding and maintaining relevant ecosystem services like soil fertility and crop productivity, but also for understanding key environmental processes intimately related with the maintenance of other regulatory ecosystem services like global climate change mitigation through carbon sequestration. An increase in temperature would accelerate the mineralization of soil organic carbon. However, the properties of organic carbon remained in soil after mineralization is not well known.

Materials and methods

Mollisol was collected at 0–20-cm depth from maize (Zea mays L.) field in Northeast China. A 180-day incubation experiment was conducted at three different temperatures (10, 30, and 50 °C) under constant soil moisture (60 % water holding capacity). Soil samples were assayed for total organic carbon (TOC), water-soluble organic carbon (WSOC), easily oxidizable organic carbon (EOC), humic fractions carbon, aggregate-associated carbon, and water stability of aggregates. Elemental analysis and solid-state 13C nuclear magnetic resonance spectroscopy were used to characterize humic acid and humin fractions.

Results and discussion

The contents of soil TOC, EOC, humic fractions carbon, and aggregate-associated carbon decreased with the increase in temperature. The proportion of 2–0.25-mm macroaggregate and the mean weight diameter (MWD) of aggregates also decreased. The C, H, N, S, alkyl C, and O-alkyl C contents of humic acid and humin decreased, whereas the O, aromatic C, and carbonyl C contents increased. The H/C, aliphatic C/aromatic C, and O-alkyl C/aromatic C ratios in humic acid and humin fractions decreased.

Conclusions

The increase in temperature has a negative impact on soil organic carbon content, soil aggregation, and aggregate stability. Moreover, humic acid and humin molecules become less aliphatic and more decomposed with the increase in temperature.
  相似文献   

9.
Because of the important role of soil organic carbon (SOC) in nutrient cycling and global climate changes, there has been an interest in understanding how different fertilizer practices affect the SOC preservation and promotion. The results from this study showed that long‐term application of manure (21 years) could increase significantly the content of SOC, total nitrogen (N) and soil pH in the red soil of southern China. The chemical structure of SOC was characterized by using solid‐state cross‐polarization magic angle spinning (CPMAS) 13C nuclear magnetic resonance (NMR) spectroscopy, and the aromatic C, ratio of alkyl C : O‐alkyl C, aromaticity and hydrophobicity of mineral fertilizers N, P and K plus organic manure (NPKM) and organic manure (M) treatments were less than those of mineral fertilizer nitrogen (N) and mineral fertilizers N, P and K (NPK) treatments. Both poorly crystalline (Feo) and organically complexed (Fep) iron contents were influenced significantly (P < 0.05) by different fertilizers, and it was observed that NPKM and M treatments increased the non‐crystalline Fe (Feo‐Fep) content. There was a significant (P < 0.01) positive correlation between soil organic C and non‐crystalline Fe in both the surface (0–20 cm) and subsurface (20–40 cm) soils. The results suggested that non‐crystalline Fe played an important role in the increase of SOC by long‐term application of organic manure (NPKM and M) in the red soil of southern China.  相似文献   

10.
A glasshouse incubation experiment was conducted to study the carbon (C) and nitrogen (N) mineralization of municipal solid waste compost (MSWC) added at differential rates to a laterite soil where cassava has been continuously cultivated for the past 10 years. The rate of C mineralization from added substrates increased with increasing rates of addition of MSWC. Available N significantly increased with increase in the rate of application of MSWC. There was a decreasing trend in E465/E665 ratio of humic acid as we increased the rate of application of MSWC from 2.5 to 20 t ha?1. The Cross Polarization Magic Angle Spinning (CPMAS) 13C NMR spectral analysis revealed that there are differences in the rate of humification of added MSWC, and application of MSWC at 15 t ha?1 resulted in least humification with the greatest alkyl C, lowest aromatic C, and greater O-alkyl C content. The decomposition rate (R) was found to be greater for this treatment. The residual C in soil was found to increase over time coincident with greater rates of MSWC application, indicating increased C stabilization, which could improve soil quality.  相似文献   

11.
The 4‐year application of pig‐manure compost (PMC) to crop fields in Jiangsu significantly increased organic‐C and total N concentrations compared to chemical fertilization and control treatment. To identify the soil processes that led to these changes, 13C cross‐polarization magic‐angle spinning nuclear‐magnetic resonance (13C CPMAS NMR) and dipolar‐dephasing nuclear‐magnetic‐resonance spectroscopy (DD NMR) were conducted on soil organic matter (SOM) fractions separated by wet‐sieving and density fractionation procedures. This allowed characterization of the SOM quality under three contrasting fertilizer regimes. The results indicate that PMC application can alter the distribution of functional groups and improve alkyl C‐to‐O‐alkyl C ratios compared to chemical‐fertilizer treatment (CF). Alkyl C contents were increased from macroaggregate fractions (> 2 mm) to microaggregate fractions (0.05–0.25 mm) for all treatments, suggesting that recalcitrant material accumulates in the microaggregate fractions. The O‐alkyl C contents were decreased from macroaggregate fractions (> 2 mm) to microaggregate fractions (0.05–0.25 mm) under CF and PMC treatments, while no consistent trend was found for the control (NF) treatment. The alkyl C‐to‐O‐alkyl C ratios in macroaggregates were lower than those in microaggregates, indicating that the degrees of SOM decomposition were lower in macroaggregates compared to microaggregates. In all aggregate‐size classes, the amount of organic matter appeared to depend on the fertilization regime. This study provides useful information regarding the buildup of organic material in soil from long‐term manure‐compost enrichment.  相似文献   

12.
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.  相似文献   

13.
硫酸铝对新开垦苏打盐碱水田的快速改良和培肥效果   总被引：3，自引：1，他引：2  
通过田间试验,研究了硫酸铝(0,300,500,900,1400kg/hm^2)施用对新开垦苏打盐碱水田的快速改良和培肥效果。结果表明:与不施用硫酸铝的对照处理相比,施用硫酸铝后土壤pH、全盐量、交换性钠、阳离子交换量和碱化度降低;可溶盐组成中,CO32-、Ca2+、K+、Na+含量通常降低,SO42-含量增加,而HCO3-、Cl-和Mg2+含量没有显著的变化,从而使得(CO32-+HCO3-)/(Cl-+SO42-)比值下降;土壤有机碳、胡敏酸碳、富里酸碳、胡敏素碳及各粒径水稳性团聚体有机碳含量均显著增加,而水溶性有机碳含量则显著降低;土壤有机碳组成中,烷基碳和烷氧碳的比例增加,而芳香碳和羰基碳的比例降低,导致烷基碳/烷氧碳和疏水碳/亲水碳比值降低而脂族碳/芳香碳比值增加;此外,土壤中>2mm水稳性团聚体和<0.053mm粉黏粒组分的比例降低,而2~0.25,0.25~0.053mm水稳性团聚体的比例增加,导致水稳性团聚体的平均重量直径降低;随硫酸铝施用量的增加,上述规律性通常表现得更为明显,但900,1400 kg/hm^2硫酸铝用量间通常没有明显的差异。说明硫酸铝施用能降低土壤碱性和盐分含量,同时有助于提高土壤有机碳含量并改善其品质,是快速改良和培肥苏打盐碱土的有效方式;但值得注意的是,硫酸铝单独施用不利于土壤结构性的改善,还需要与其他改良措施配合使用。  相似文献   

14.
Abstract

Although the application of manure to upland fields is believed to induce changes in the quality of humic substances in soil as well as the quantity, the direction and extent of these changes have not been elucidated. To understand temporal variations in humic acids, periodically collected soil samples from two fields, a Typic Hapludult (Togo) and a Pachic Melanudand (Kuriyagawa), with cattle manure and chemical fertilizer (CF) were examined. The content and degree of humification (darkening) of the humic acids were distinctly greater in Kuriyagawa than in Togo soil. Corresponding to the difference in the degree of humification, molecular size distribution, elemental composition, infrared (IR) spectra, and 13C cross polarization/magic angle spinning nuclear magnetic resonance (CPMAS NMR) spectra of humic acids differed between the two soils. Manure application at 40 Mg ha?1 year?1 for 16 years (Togo) and at 80 or 160 Mg ha?1 year?1 for 19 years (Kuriyagawa) resulted in greater humic acid content compared with plots with CF only because of its increase in the manured plots and/or decrease in the CF plots. Manure application at an extremely high rate (160 Mg ha?1 year?1) resulted in higher H content and greater signal intensities of alkyl C, O-alkyl C and amide C=O in the 13C CPMAS NMR and/or IR spectra. Although humic acids with larger molecule sizes increased in all the manured plots, differences between the humic acids from the plots with and without manure applied at practical levels in the elemental and spectroscopic analyses were small or scarce. These results were considered to be because of the similarity between the indigenous soil humic acids and the manure-derived ones in Togo soil (a low degree of humification) and because of the abundance of highly-humified humic acids in Kuriyagawa soil.  相似文献   

15.
We have tested to see if the generic set of NICA‐Donnan model parameters, used to describe isolated humic substances, can also describe soil humic substances in situ. A potentiometric back‐titration technique was used to determine the variable surface charge of two organic peat soils at three different ionic strengths. The non‐ideal, competitive‐adsorption NICA‐Donnan model was used to simulate the surface charge, by assuming a bimodal distribution of H+ affinity on the soil solid phase. The model provided an excellent fit to the experimental data. The Donnan volume, VD, varied slightly with ionic strength, although the variation was less than for humic substances in solution. The values obtained for the parameters that define the affinity distributions, the intrinsic proton binding constant (log Kiint) and the heterogeneity of the site (mi), were similar to those observed for isolated soil humic acids. The abundance of carboxylic groups in the whole soil represented 30% of the typical value for isolated soil humic acids. The composition of the organic matter of the whole soils, obtained by 13C CPMAS NMR, was comparable to the characteristic composition of soil humic acids.  相似文献   

16.
《Geoderma》2006,130(1-2):124-140
Chemically and physically fractionated samples extracted from the surface horizon of a soil developed under a mix of coniferous and deciduous vegetation in southwestern Colorado were studied. 13C NMR data on this soil's organic matter and its HF(aq)-washed residue, as well as the classic acid/base-separated humic fractions (humic acid, fulvic acid, humin), were examined for chemical–structural detail, e.g., the various structural functionalities present (especially lipids, carbohydrates, aromatics, polypeptides and carbonyl/carboxyls). Among the humic fractions, it was found that the lipid concentrations are in the order humic acid>fulvic acid= humin; for carbohydrates the order is fulvic acid>humin>humic acid; for aromatic carbons the order is humic acid>humin>fulvic acid; for polypeptides it is humic acid>fulvic acid>humin and for carbonyl/carboxyl species it is humin>humic acid>fulvic acid, but the differences are small. 13C spin–lattice relaxation times indicate that at least two types of “domains” exist in each, corresponding to “higher” and “lower” concentrations of paramagnetic centers, e.g., Fe3+.  相似文献   

17.
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   

18.
Soils from A horizons of Eutrochrepts under spruce forest (Sf), mixed deciduous forest (Df), permanent grassland (Gp), and arable rotation (Ar) were fractionated into clay- (<2 μm), silt-(2–20 μm) and sand- (20–2000 μm) sized separates. 13C NMR spectroscopy was used to compare SOM composition across size separates and between land-use regimes. CPMAS 13C NMR spectroscopy showed that the intensity of signals assigned to carbohydrates (representing most O-alkyl C) and lignin (phenolic and methoxyl C) declined with decreasing particle size. Concurrently, alkyl C and C-substitution of aromatic C increased in the order sand, silt, clay. The amount of alkyl C correlated well with microbial resynthesis of carbohydrates. Solution 13C NMR spectra suggested that humic acids (HA) extracted from the size separates were richer in carboxyl C and aromatic C than the bulk size separates. Also HA reflected increasing percentage of alkyl C with decreasing particle size. O-alkyl C were lower in silt HA than in clay HA whereas aromatic C tended to peak in silt HA. These results suggested that sand-sized separates were enriched in plant residues (primary resources) whereas clay-sized separates were dominated by products of microbial resynthesis (secondary resources). Silt was rich in selectively preserved and microbially transformed primary resources. 13C NMR spectroscopy showed only small differences in SOM composition between land-use regimes, except that silt and silt HA from Ar were richer in aromatic C than those from the other plots. But enrichment factors (E= content in fraction/content in whole soil) revealed differences in the distribution of C species across the size separates. Relatively high Earomatic (0.9) and Eo-alkyl (1.0) for sand from Gp indicated high amounts of plant residues, probably due to intense rhizodeposition and to occlusion of plant debris within aggregates. Low Earomatic (0.3) and Eo-alkyl (0.3) for sand from Ar suggested depletion of primary resources, which could be attributed to disintegration of soil aggregates upon cultivation. A pronounced enrichment of alkyl C in Ar clay-sized separates (Ealkyl= 3.1) suggested large amounts of microbial carbon. Microbial products attached to clay surfaces by a variety of physico-chemical bondings appeared more stable against mineralization induced by cultivation than plant residues sequestered in aggregates.  相似文献   

19.
The definition of humusforms from soils under cultivation. II. Quantity and quality of soil organic matter In the new edition of the German textbook “Practical Studies in Soil Science” the authors presented a proposal of mapping humusforms in arable soils in order to characterize soil and site ecology (Schlichting et al., 1995). This proposal was developed from the definitions “Ochric”, “Mollic” and “Umbric” of the Soil Taxonomy and the FAO classification. The characterization of humusforms in 45 arable surface soils was carried out according to this proposal while soil organic matter (SOM) composition was investigated by means of wet chemistry and CPMAS 13C-NMR spectroscopy. “Mollic” in contrast to “Umbric” humusforms could be characterized by a higher carbonyl/carboxyl carbon content probably deriving from proteins, polysaccharides and humic substances. In addition the mollic epipedon contains 10% more litter compounds, whereas in the umbric epipedon humic acids are of major importance. The humin fraction in the mollic epipedon is thought to be raised by the formation of Ca-humates. Our data suggest, that with regard to microbial decomposition a surplus of available organic matter is present in the mollic horizons. The ochric-like epipedon has a much lower humus content compared to “Mollic” and “Umbric” horizons and exhibits the highest amounts of soluble organic matter as well as aromatic and carboxylic C-compounds in the humic fraction. Our data suggest, that SOM quantity and quality of the mollic, umbric and ochric epipedons differ substantially. These findings suggest that the proposal of Schlichting et al. (1995), which was extended by Blume & Beyer (1996), should be regarded as a useful basis to discuss the development of humusforms in soils under cultivation and facilitate soil survey in order to improve site characterization.  相似文献   

20.
Rock fragments in soil can contain significant amounts of organic carbon. We investigated the nature and dynamics of organic matter in rock fragments in the upper horizons of a forest soil derived from sandstone and compared them with the fine earth fraction (<2 mm). The organic C content and its distribution among humic, humin and non‐humic fractions, as well as the isotopic signatures (Δ14C and δ13C) of organic carbon and of CO2 produced during incubation of samples, all show that altered rock fragments contain a dynamic component of the carbon cycle. Rock fragments, especially the highly altered ones, contributed 4.5% to the total organic C content in the soil. The bulk organic matter in both fine earth and highly altered rock fragments in the A1 horizon contained significant amounts of recent C (bomb 14C), indicating that most of this C is cycled quickly in both fractions. In the A horizons, the mean residence times of humic substances from highly altered rock fragments were shorter than those of the humic substances isolated in the fine earth. Values of Δ14C of the CO2 produced during basal respiration confirmed the heterogeneity, complexity and dynamic nature of the organic matter of these rock fragments. The weak 14C signatures of humic substances from the slightly altered rock fragments confirmed the importance of weathering in establishing and improving the interactions between rock fragments and surrounding soil. The progressive enrichment in 13C from components with high‐14C (more recent) to low‐14C (older) indicated that biological activity occurred in both the fine and the coarse fractions. Hence the microflora utilizes energy sources contained in all the soil compartments, and rock fragments are chemically and biologically active in soil, where they form a continuum with the fine earth.  相似文献   

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