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1.
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   

2.
ABSTRACT

Sugarcane is a strategic commodity in Indonesia. It is usually raised in a monoculture system. There is a lack of information about the effects of extended sugarcane monoculture on the soil carbon fraction. The aim of this study was to determine the relative changes in the soil organic C fractions in response to the duration of sugarcane monoculture on Entisols, Inceptisols, and Vertisols. The measured variables were the percentages of sand, silt, and clay, organic matter (OM), total nitrogen (TN), pH (H2O), cation exchange capacity (CEC), NH4 +, NO3 -, labile carbon fraction (soil carbon mineralization (C-Min), soil microbial carbon (C-Mic), and carbon particulate organic matter (C-POM)), and stable carbon fraction (humic and fulvic acids). Soil type with sugarcane monoculture period had significant influences on the percentages of clay, sand, silt, CEC, and pH (H2O). Soil type and sugarcane monoculture period had no apparent significant effect on C-Min or C-POM but did significantly influence C-Mic. The humic and fulvic acid levels in all three soil types were affected by the duration of sugarcane monoculture. To establish the impact of long-term sugarcane monoculture on the physicochemical properties of soils with various textures, it is more appropriate to measure the soil stable carbon fractions such as humic and fulvic acid rather than the soil labile carbon fractions such as C-Min, C-POM, or C-Mic.  相似文献   

3.
To investigate the chemical heterogeneity of humic substances in relation to molecular size, fulvic and humic acids were extracted and purified from the surface horizon of a Humic Gleysol in northern Switzerland. A fractionation scheme using hollow‐fibre ultrafiltration cartridges was developed and used to obtain four size fractions of the humic acid with nominal molecular weight ranges > 300 kDa, 100–300 kDa, 30–100 kDa, and 10–30 kDa. The fulvic acid and all humic acid fractions were characterized by size exclusion chromatography, elemental analysis (C, H, N, S), as well as spectroscopic techniques including UV‐VIS, CP‐MAS 13C‐NMR, FT‐IR, and fluorescence spectroscopy. Clear chemical differences between the humic acid size fractions were observed. Smaller size fractions of the soil humic acid contained more chargeable functional groups and a larger percentage of aromatic carbon than the larger size fractions. Conversely, the percentage of aliphatic carbon increased with increasing apparent molecular weight. The chemical composition of the smallest humic acid fraction differed clearly from the fulvic acid fraction, despite similar apparent molecular size and carboxyl carbon content. Small humic acids contained much more aromatic carbon and less aliphatic carbon than the fulvic acid fraction. Apparently, humic size fractions differ in their chemical composition, which can have important implications for their environmental behaviour.  相似文献   

4.
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   

5.
The carbohydrates in soil organic matter seem to be derived from undecomposed or partially decomposed plant and microbial residues, In soil, these carbohydrates exist chiefly in such from as polysaccharide hemicellulose, and their polyuronide has been the chief object of investigation1)-3). In various soil, the polyuronide is found in a large quantity in fulvic fraction of soil organic matter and has been considered as important in connection with the physical structure of soil4),5). According to Lynch 5), the carbohydrate content of humic acid is markedly smaller than that of fulvic acid. His work also indicates that a' considerable change is noted in the content and composition of the carbohydrate in humic acid because of the addition of some organic substances to the soils, or of the cultivation of virgin soils. Further, some investigators7) believe that uronic acid is introduced into the aromatic structure of the humic acid by changing into pentose and furan. Accordingly, it seems that the role of carbohydrate in the formation of soil humic acid should not be overlooked.  相似文献   

6.
The most southerly ombrotrophic peat bogs in Europe are in Galicia (northwest Spain). The humic matter in them originates from chemical processes in anaerobic conditions. We studied the acid properties of fulvic acids and humic acids isolated from two peat horizons of an ombrotrophic peat bog by potentiometric titration. Solutions containing 25, 50 and 100 mg l−1 of each humic substance were titrated at ionic strengths 0.005 m , 0.01 m and 0.1 m (with KNO3 as the inert electrolyte). Charge curves were analysed with a Donnan model to determine the intrinsic proton binding parameters. The concentration of the humic substance affected the charge curves more significantly at pH exceeding 6, and tended to disappear at greater concentrations. The proton binding conditional constants decreased with increasing ionic strength, this effect being more significant in the carboxylic groups with less affinity for protons. The proton binding constant of the carboxyl groups in a fulvic acid was one order of magnitude less than the value for the corresponding humic acid, whereas for the phenolic groups the values for both fractions were similar. The total content of acid groups was approximately 2 mol kg−1 greater in the fulvic fraction than in the humic fraction. Both humic fractions from the lower horizon contained more acid groups than those from the upper horizon, mainly because the content of carboxyl groups increases with soil depth. Therefore, the humic substances in the lower horizon of the peat will be more negatively charged, which will affect their solubility and the binding of metal ions.  相似文献   

7.
Incorporation of newly-immobilized N into major soil organic matter fractions during a cropping period under paddy and upland cropping systems in the tropics was investigated in Jawa paddy fields with and without fish cultivation and a Sumatra cassava field in Indonesia. 15N-labelled urea (15N urea) was applied as basal fertilizer, and the soil samples were collected after harvest. The percentage of distribution of the residual N in soil from 15N urea into the humic acids, fulvic acid fraction, and humin were 13.1–13.9, 19.0–20.5, and 53.4–54.3%, respectively, for the Jawa paddy soils, and 14.9, 27.4, and 52.4%, respectively, for the Sumatra cassava soil. These values were comparable to the reported ones for other climatic zones. The percentage of distribution of 15N urea-derived N into humic acids was larger than that of total N into the same fraction in all the soils. The distribution into the fulvic acid fraction was also larger for 15N urea-derived N than for total N in the Jawa soils. Humic and non-humic substances in the fulvic acid fraction were separated using insoluble polyvinylpyrrolidone (PVP) into the adsorbed and non-adsorbed fractions, respectively. Less than 5% of the 15N urea-derived N in fulvic acid fraction was detected in the PVP-adsorbed fraction (generic fulvic acids). The proportion of non-hydrolyzable N remained after boiling with 6 M HCl in the 15N urea-derived N was 9.4–13.5%, 17.3–26.7%, and 8.4–16.6% for the humic acids, generic fulvic acids, and humin, respectively. The significantly low resistance to acid hydrolysis suggested that the 15N urea-derived N was less stable than the total N in soil regardless of the fractions of humus.  相似文献   

8.
红松人工林腐殖质组成及其结合形态研究   总被引：4，自引：0，他引：4       下载免费PDF全文
 运用野外调查与实验分析相结合的方法,对不同生长发育阶段红松人工林（林龄25、45、58、68 a）和红松混交林（林龄60a）根际与非根际土壤有机质含碳量、腐殖质组成与结合形态进行了研究。结果表明:不同年龄阶段红松人工纯林、红松混交林土壤有机质含碳量、腐殖质各组分含碳量随土层深度的加深而降低,并且根际土壤高于非根际土壤。就土壤腐殖质组成而言,除林龄58a红松人工林根际土壤和45a红松人工林非根际土壤外,其他林型土壤胡敏酸含碳量均高于富里酸含碳量;胡敏酸与富里酸比值（HA/FA）在1.00～2.45之间;土壤重组腐殖质、松结态腐殖质、稳结态腐殖质含碳量大小顺序为林龄58>68>25>45a;红松混交林除紧结态腐殖质外,其他腐殖质各组分含碳量均高于红松人工林。  相似文献   

9.
《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   

10.
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11.
Volcanic ash soils along the western edge of the Omiya tableland, Japan, are covered with thick anthropogenic soil horizons. The formation of anthropogenic soil horizons occurs because of the soil dressing practice known as “Dorotsuke,” where alluvial soil materials are deposited on fields and mixed with volcanic ash topsoil by tillage over the years. To clarify the chronology of this anthropedogenesis, carbon-14 (14C) age profiles were estimated using humic acid fractions from three pedons: an anthropogenic soil, an undressed Andosol, and a Fluvisol. Soil charcoal fragments were also dated to estimate maximum burial age. Charcoal fragments displayed vertically random age distributions, indicating that the fragments may have had multiple origins. However, the age of charcoal in the lower part of the anthropogenic soil horizons indicated that the initiation of anthropedogenesis occurred later than the late 13th century. The 14C age profile of humic acid in the Andosol exhibited little variation in age with depth in the subsoil. The 14C age profile of humic acid in the Fluvisol suggested that the humic acid fraction included allochthonous old carbon (C), although the soil itself had been formed from recent sediments. The 14C age profile of humic acid in the anthropogenic soil showed features of its two component soils. The 14C ages in the volcanic ash subsoil matched with those in the Andosol, whereas the ages increased in the anthropogenic soil horizons because of supplementation with old C from alluvial soil materials. However, the peak 14C ages occurred in the lower part of the anthropogenic horizons, whereas the middle part on the peak position displayed a gradual age-depth gradient. This feature was interpreted as a sign of 14C activity equilibrium throughout anthropedogenesis. On the basis of this postulated 14C activity equilibrium, the linear age-depth gradient at the peak position was derived from differences in burial time, and burial ages were calculated by estimating steady-state 14C. The calculated ages were lower than the charcoal ages. These age estimates suggest that anthropedogenesis was initiated in the Middle Ages and reached an intermediate stage before or during the first half of the Edo period.  相似文献   

12.
Humic substances are the main responsible for soil conditioning and are one of the major components of the composting product. However, there is still little information about their composition and mechanisms of activity. This study aimed to evaluate quantitatively the humic and fulvic fraction by size-exclusion liquid chromatography and the metal content by atomic absorption spectrometry. The chromatographic method used was efficient for humic and fulvic acids quantitation. Levels of 1.73 ± 0.03 and 1.6 ± 0.5 g kg?1 were found for chicken manure regarding humic and fulvic acids, respectively, and 5.1 ± 0.9 and 1.2 ± 0.1 g kg?1 for peat. The metal contents indicated the need of a mineral enrichment, because only the levels of iron reached the minimum recommended by legislation. It was also observed that evaluated organic fertilizers were in accordance with the specifications established by legislation in relation to carbon and total nitrogen and the pathogen levels.  相似文献   

13.
Studies were made to determine the rate of decomposition of some 14C-labeled microbial polysaccharides, microbial cells, glucose, cellulose and wheat straw in soil, the distribution of the residual 14C in various humic fractions and the influence of the microbial products on the decomposition of plant residues in soil. During 16 weeks from 32 to 86 per cent of the C of added bacterial polysaccharides had evolved as 14CO2. Chromobacterium violaceum polysaccharide was most resistant and Leuconostoc dextranicus polysaccharide least resistant. In general the polysaccharides, microbial cells, and glucose exerted little effect on the decomposition of the plant products. Upon incubation the 14C-activity was quickly distributed in the humic. fulvic and extracted soil fractions. The pattern of distribution depended upon the amendment and the degree of decomposition. The distribution was most uniform in the highly decomposed amendments. After 16 weeks the bulk of the residual activity from Azotobacter indicus polysaccharide remained in the NaOH extracted soil. From C. violaceum polysaccharide both the extracted soil and the humic acid fraction contained high activity. About 50–80 per cent of the residual activity from the 14C-glucose, cellulose and wheat straw amended soils could be removed by hydrolysis with 6 n HCl. The greater part of this activity in the humic acid fraction was associated with the amino acids and that from the fulvic acids and residual soils after NaOH extraction with the carbohydrates. About 8 16 per cent of the activity of the humic acid fraction was present in substances (probably aromatic) extracted by ether after reductive or oxidative degradation.  相似文献   

14.
为探究生物炭对土壤腐殖质组成和团聚体特征的影响，以东北黑土区植烟土壤为研究对象，设置了3个处理，2019-2020年连续施用低量生物炭5t/hm2（C1）；高量生物炭25t/hm2（C2）和不施生物炭（CK），分析了不同用量生物炭对土壤腐殖质组分及水稳性团聚体分布的影响，并利用傅里叶红外光谱(FTIR)和13C核磁共振光谱(13C-NMR)对土壤胡敏酸化学结构进行表征。结果表明：C1和C2处理分别使富里酸减少了16.90%和40.85%，胡敏酸含量显著增加了14.86%和33.78%，胡敏酸在腐殖酸中所占比例（PQ值）也显著增加；FTIR和13C-NMR分析表明，C2处理的土壤胡敏酸的2920/1620值降低了11.82%，脂族C/芳香C比值降低了13.04%，表明高量生物炭使胡敏酸芳构化程度增强，脂肪结构比例降低；生物炭的添加促使土壤大团聚体（>0.25mm）比例增加，C2处理提升大团聚体的作用更显著。结合相关性分析发现，胡敏酸含量与2~0.25mm大团聚体含量显著正相关，胡敏酸分子的脂肪族官能团特征与>2mm粒级团聚体显著正相关。此外，C1和C2处理显著提高了烟叶产量。从而表明，生物炭能提升土壤腐殖质中胡敏酸含量和结构，有利于土壤大团聚体形成，提高土壤固碳潜力，对作物有一定的增产效果。  相似文献   

15.
The 18O/16O ratios of a number of soil humic and fulvic acids were measured and compared with those of lignin and cellulose samples originating from the same area. The average enrichments above ground water were: cellulose 32%0 humic and fulvic acid 29%0 and lignin 14%0, suggesting that the oxygen in humic and fulvic acid originates pricipally from cellulose or other plant carbohydrates and not lignin as has been suggested.  相似文献   

16.
In order to analyze the behavior and phytoxicity of iodine in soil, the chemical forms of soil iodine must be identified. Therefore, a method for quantitative speciation of iodine in soil was proposed. Iodine extracted from soil samples with tetrametBPyIammonium hydroxide (TMAH) was separated into humic and fnalvic acid fractions at pH4 1.5 after the addition of ascorbic acid into the TMAH extract to reduce iodate into iodide. Since the iodide in the TMAH extract was recovered in the fdvic acid fraction by this procedure, iodine contained in the haamic acid fraction was considered to be organically bound. Podine in the fulvic acid fraction was separated into organic iodine bound to fnlvic acids and the total inorganic iodine. Furthermore, iodine soluble from soil in 0.1 mol L-1 potassium chloride was assumed to correspond to the amount of total iodide in soil, and from the difference in the concentration of total inorganic iodine and soluble iodide, the amount of iodate was calculated. By the application of this method, iodine in soil was separated into four fractions: organic iodine bound to humic acids, organic iodine bound to fulvic acids, iodate, and iodide. This speciation method was applied to two soils. It was found that s Barge proportion of iodine in soil occurred in an organicalPy bound form.  相似文献   

17.
Abstract

Organic matter in Urbic Anthrosols often contains chemically and biologically inert organic carbon. This material, called black carbon (BC), originates from municipal wastes, coal‐mine deposits and/or fly ash. This black carbon needs to be differentiated from the other soil organic substances because of its very different physical and chemical nature. In this paper, we propose a new method for determining BC, integrated into the humic fractionation procedure. The remaining organic carbon in the soil residue left after lipid extraction, alkaline extraction [0.5 M sodium hydroxide (NaOH)], and further oxidation with 30% hydrogen peroxide (H2O2) is defined as inert organic carbon or BC. The common fractions of soil organic matter, such as lipids, fulvic and humic acids, and humins are thus supplemented with a new fraction, BC. According to our results by 13C‐NMRspectroscopy, this fraction consists mainly of polyaromatic hydrocarbons with few functional groups.  相似文献   

18.
Organic wastes such as sewage sludge and compost increase the input of carbon and nutrients to the soil. However, sewage sludge-applied heavy metals, and organic pollutants adversely affect soil biochemical properties. Therefore, an incubation experiment lasting 90 days was carried out to evaluate the effect of the addition of two sources of organic C: sewage sludge or composted turf and plant residues to a calcareous soil at three rates (15, 45, and 90 t of dry matter ha–1) on pH, EC, dissolved organic C, humic substances C, organic matter mineralization, microbial biomass C, and metabolic quotient. The mobile fraction of heavy metals (Zn, Cd, Cu, Ni, and Pb) extracted by NH4NO3 was also investigated.The addition of sewage sludge decreased soil pH and increased soil salinity to a greater extent than the addition of compost. Both sewage sludge and compost increased significantly the values of the cumulative C mineralized, dissolved organic C, humic and fulvic acid C, microbial biomass C, and metabolic quotient (qCO2), especially with increasing application rate. Compared to compost, the addition of sewage sludge caused higher increases in the values of these parameters. The values of dissolved organic C, fulvic acid C, microbial biomass C, metabolic quotient, and C/N ratio tended to decrease with time. The soil treated with sewage sludge showed a significant increase in the mobile fractions of Zn, Cd, Cu, and Ni and a significant decrease in the mobile fraction of Pb compared to control. The high application rate of compost resulted in the lowest mobility of Cu, Ni, and Pb. The results suggest that biochemical properties of calcareous soil can be enhanced by both organic wastes. But, the high salinity and extractability of heavy metals, due to the addition of sewage sludge, may limit the application of sewage sludge.  相似文献   

19.
Abstract

The changes in quality and quantity of phenolic substances in the decaying process of rice straw in a soil were compared under moist and flooded conditions for 200 days. The amounts of phenolic substances divided into fractions of humic acid and fulvic acid, ether- and butanol-extractable and organic solvent-unextractable fractions, then the amounts of individual phenolic acids were determined. The following results were obtained.

1) Alkali-extractable total phenolics as well as individual phenolic acids decreased more rapidly under moist, than under flooded, conditions as rice straw decayed in the soil. The phenolics present were mainly attributable to the straw, not to the soil.

2) The decrease in the level of total phenolics in the early stage of the decaying process was mainly due to the decrease in ether-extractable phenolic compounds in the fulvic acid fraction, and in the later stage, was mainly due to the decrease in butanol-extractable phenolics in the humic acid fraction.

3) The amounts of butanol-extractable phenolics and organic solvent-unextractable phenolics were larger in humic acid than in fulvic acid. On the other hand, a larger amount of organic solvent-extractable phenolics, especially ether-extractable phenolics, was present in fulvic acid.

4) The degradation patterns and pathways of individual phenolic acids in the decaying process of rice straw in soil were found to be the lame as those of decaying straw without soil which were reported previously.

5) The level of phenolic substances in the humic acid was not greatly changed during the decaying process, but the phenolic substances in fulvic acid rapidly increased for 30 days and then rapidly decreased to a constant level.  相似文献   

20.
不同施肥措施对白土腐殖质组成的影响   总被引：3，自引：0，他引：3  
吴萍萍  王家嘉  李录久 《土壤》2016,48(1):76-81
以白土稻区4年大田定位试验为基础,设置2种翻耕深度(10 cm、20 cm,分别标记为T10、T20)和4种施肥措施(单施化肥、化肥+畜禽粪肥、化肥+秸秆还田、化肥+绿肥,分别标记为F、F+M、F+S、F+G),通过腐殖质组成修改法分别提取表层土壤水溶性物质、胡敏酸、富里酸和胡敏素,研究不同施肥措施对白土腐殖质各组分碳含量的影响。结果表明:单施化肥措施下,翻耕20 cm处理(T20+F)土壤总有机碳和腐殖质各组分碳含量均低于翻耕10 cm处理(T10+F),但差异未达显著水平。在翻耕20 cm的基础上增施有机肥能显著提高土壤总有机碳和腐殖质各组分碳含量,增施畜禽粪(T20+F+M)、秸秆还田(T20+F+S)和增施绿肥(T20+F+G)3处理的土壤总有机碳、胡敏酸、富里酸和水溶性物质碳含量较T20+F处理分别提高14.57%~30.64%、10.36%~30.57%、0.74%~12.31%和14.25%~26.80%。增施有机肥显著提高胡敏素碳含量,T20+F+M、T20+F+S和T20+F+G处理较T20+F处理提高18.87%~35.78%。4年不同翻耕与施肥措施对白土腐殖质性质未产生显著影响。增施有机肥能一定程度上提高土壤PQ值、胡富比、E4/E6值和色调系数。相关性分析表明,胡敏素、胡敏酸、富里酸碳含量与总有机碳含量间均存在显著或极显著正相关,与水溶性物质碳含量间无明显相关性。  相似文献   

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