首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到19条相似文献,搜索用时 78 毫秒
1.
不同生物质材料对蕉园土壤有机质组成的影响   总被引:2,自引:1,他引:1  
为探究不同生物质材料对蕉园土壤有机质及组成的影响,以木炭、椰壳炭、椰糠炭和与椰糠炭等碳量的椰糠为材料,分别以质量分数为2%和4%的用量加入土壤中,于室内常温培养并保持土壤含水量不变。在第15、30、60、90、120和180 d采集土壤,分析不同生物质材料对土壤有机质、胡敏酸、富里酸和土壤胡敏酸/富里酸的影响。结果表明:添加木炭、椰壳炭、椰糠炭和椰糠均能提高土壤有机质含量,并随添加量的增加而升高;添加木炭、椰壳炭、椰糠炭和椰糠均能加速土壤有机质的分解,添加椰壳炭对土壤有机质分解的影响相对较小。椰糠的添加主要是同时增加了土壤胡敏酸和富里酸碳含量,生物炭(木炭、椰壳炭和椰糠炭)的添加主要是影响了土壤胡敏酸与富里酸的相互转化。  相似文献   

2.
不同来源腐殖酸的组成和性质的研究   总被引:31,自引:1,他引:30  
贺婧  颜丽  杨凯  马明贺  刘晔  崔桂芳 《土壤通报》2003,34(4):343-345
本研究从三种有机物料草炭、褐煤、风化煤中提取腐殖酸,对其组成和性质进行了测定,同时对胡敏酸进行酒精沉淀分级。研究结果表明:褐煤胡敏酸氧化度和芳香度最高,其次为风化煤胡敏酸,最后是草炭胡敏酸;风化煤富里酸的氧化度和芳香度最高,其次为褐煤富里酸和草炭富里酸。胡敏酸各级分的回收率均随着级分数的升高而增加。回收率以风化煤胡敏酸最高,依次为褐煤胡敏酸、草炭胡敏酸。  相似文献   

3.
为了探究天然有机质结构对有机污染物光降解的影响,选取7种天然有机质,在以氙灯为光源模拟太阳光条件下,研究这7种天然有机质对菲、诺氟沙星光解的影响。菲、诺氟沙星在纯水中光化学降解反应均符合准一级动力学。加入胡敏酸组分的溶液中菲、诺氟沙星降解速度普遍大于加入富里酸组分的溶液中菲、诺氟沙星的降解速度。黑土富里酸、胡敏酸之间结构差异较大,有机肥富里酸、胡敏酸之间结构差异较小。将天然有机质结构特征与菲、诺氟沙星降解系数进行相关性分析得出,胡敏酸类有机质比富里酸类有机质腐殖化程度更高,吸光能力更强,更容易吸收光子跃迁到激发三重态,将能量传递给基态污染物,促进菲、诺氟沙星更快地降解。  相似文献   

4.
特定培养条件下土壤有机质分解转化规律的研究   总被引:8,自引:0,他引:8  
通过室内培养实验,应用δ~(13)C方法研究了玉米秸秆分解期间,土壤固有及新形成有机质的分解转化规律。结果表明:玉米秸秆分解期间,土壤固有及新形成的有机质都逐渐分解,但前者的分解速度较慢。第360 d时,玉米秸秆和土壤固有有机质的残留率分别为30.0%和92.2%;720 d时分别为25.3%和78.8%。培养初期,富里酸的形成速度大于胡敏酸,而后富里酸转化为胡敏酸或相互转化;与新形成有机质相比,固有有机质中胡敏酸、富里酸的转化速度相对较慢。  相似文献   

5.
土壤腐殖质分组研究   总被引:23,自引:1,他引:22  
采用Pallo法对两种耕地土壤腐殖质进行分组,初步研究了各组分的数量和结构特征。结果表明:焦磷酸钠提取的胡敏酸(HAp)是胡敏酸(HA)的主要组分;游离富里酸(FAf)是富里酸(FA)的主要组分;胡敏素(HM)的主要组分为非溶解性胡敏素(ISHM),而溶解性胡敏素(SHM)含量较低。通常随土层深度增加,HA、HM各组分的绝对数量和相对数量都下降;FA各组分的绝对数量也下降,而相对数量增加;HA/FA比值下降。一般来看,焦磷酸钠提取的富里酸(FAp)、氢氧化钠提取的富里酸(FAs)比相应的HAp、氢氧化钠提取的胡敏酸(HAs)的分子结构简单,铁结合胡敏素(HMi)比粘粒结合胡敏素(HMc)的分子结构简单;随土层深度增加,HAp、HAs的分子结构变简单,而HMi、HMc的分子结构变复杂。  相似文献   

6.
热辐射对水稻土有机质组成的影响   总被引:1,自引:0,他引:1  
黄兆琴  胡林潮  代静玉 《土壤》2009,41(4):630-634
本文研究了受不同程度热辐射后的水稻土中有机质组分的变化情况,结果表明:随温度升高,土壤中水溶性有机碳(DOC)含量先增加后减少,200℃变化尤为显著,增加为CK的3.68 ~ 7.45倍,中性糖、糖醛酸与DOC的变化趋势一致.辐射温度不同,土壤中的胡敏酸、富里酸组成和含量亦发生不同程度的变化,300℃胡/富比值最大(1.79 ~ 5.04),土壤腐殖质聚合程度增加;200℃胡敏酸的E4/E6比值最大,反映此温度下土壤芳香缩合度低、具有较多的脂族结构物质、土壤腐殖化程度低.  相似文献   

7.
黄土丘陵区不同植被下土壤可溶性有机物的荧光特征研究   总被引:4,自引:0,他引:4  
【目的】土壤水溶性有机质的组成和结构是土壤质量的重要判别指标,具有重要的生态意义。研究黄土丘陵地区不同植被下土壤水溶性有机物的数量和荧光结构特征,可以为该地的植被修复及土壤质量评价提供科学依据。【方法】利用传统荧光和三维荧光技术,选取激发发射荧光光谱、 同步荧光光谱得到的腐殖化指标对土壤水溶性有机物的来源和结构进行评估,通过三维荧光技术探究不同植被下土壤水溶性有机物之间组分的差异。【结果】辽东栎(Quercus liaotungensis)和油松林(Pinus tabulaeformia)地具有较高的水溶性有机物含量,含量均为0.16 mg/g; 而荒坡地和农地的水溶性有机物较低,分别为0.04和0.05 mg/g,灌木荆条(Vitex negundo var. heterophylla )和狼牙刺(Sophora viciifolia)林地的含量介于两者之间。发射激发荧光光谱、 同步荧光光谱以及三维荧光光谱表明土壤水溶性有机物大多来源于植物和微生物的混合作用; 油松林地的水溶性有机物结构较简单、 腐殖化程度较低; 而灌木林地的水溶性有机物结构较为复杂、 腐殖化程度较高。从不同植被下土壤水溶性有机物的组成来看,蛋白类的物质差异不明显; 油松和辽东栎林地土壤水溶性有机物的类酪氨酸蛋白质、 类色氨酸蛋白质、 类溶解性微生物代谢产物含量较高,灌木林地较低。最主要的差异是富里酸类和胡敏酸类物质,油松林地的水溶性小分子量的富里酸类物质占主导地位,而灌木林地的水溶性有机物芳香化程度较高,农地和抛荒地类富里酸物质和类胡敏酸类物质含量的比值最低,其水溶性腐殖质的缩聚度高。油松、 辽东栎林地水溶性有机物由于植物残体分解形成的富里酸较易被氧化,同时阴坡林地较高的含水量使得这些产物较难缩合; 而灌木林地和农田及荒地较为干旱,枯枝落叶少,腐殖酸有充分时间进行缩合,导致了水溶性有机物的高芳香化和腐殖化。【结论】不同植被下的土壤水溶性有机物的组成和结构是存在差异的,同时说明荧光技术可用于揭示水溶性有机物的组成和缩合特性研究。  相似文献   

8.
土壤中溶解性有机质分组组分的结构特征研究   总被引:18,自引:3,他引:15       下载免费PDF全文
以Leenheer的分组方法为基础 ,用XAD 8树脂将黄泥土中水溶性有机质 (DOM)按极性和电荷特性分为结构较为均一的不同组分 ,并采用元素分析、1 H NMR以及CP/MAS1 3 C NMR研究各组分的性质。初步认为 :三种不同利用方式下 (桑园、水田、水杉 )黄泥土中的DOM组成中疏水碱性组分 (HOB)含量很少 ,疏水中性组分 (HON)相对含量为 7%~ 1 5 %,亲水性组分 (HIM)是土壤DOM中最大组成部分 ,约占 35 %。元素分析、1 H NMR以及1 3 C NMR分析结果表明 :DOM各组分结构特征差异显著。HON以含有大量的长链烷烃为主要结构特征 ,并含有较多氨基酸、多肽类物质 ;疏水酸性组分 (HOA)的结构特征相似于土壤FA ,含有大量羧基 ,但与FA相比芳香族物质减少 ,碳水化合物增多 ;酸不溶组分 (AIM)以多酚类、腐殖质结合的碳水化合物为主要组成物质 ;HIM中则含有大量碳水化合物。  相似文献   

9.
蜉金龟堆肥施入后土壤腐殖质表征及特性研究   总被引:2,自引:1,他引:1       下载免费PDF全文
康露  陈贺  王富兰  吴景贵 《土壤》2014,46(3):452-457
采用元素组成、红外光谱及差热分析对土壤施用蜉金龟堆肥后腐殖质结构特征的变化进行表征。元素分析结果表明,与对照处理相比,土壤施用蜉金龟堆肥后焦磷酸钠浸提胡敏酸(NaHA)、氢氧化钠浸提胡敏酸(PAHA)、焦磷酸钠浸提富里酸(NaFA)及氢氧化钠浸提富里酸(PAFA)的碳含量增加,H/C减小,表明施肥后土壤腐植酸(胡敏酸和富里酸)的芳香性增加。差热分析结果表明,与NaHA相比,对照处理和施蜉金龟堆肥PAHA的高温放热峰消失,说明PAHA的热稳定性低于NaHA;而NaFA在两种处理中的中温反应热也均高于PAFA,进一步说明了氢氧化钠浸提腐植酸的热稳定性高于焦磷酸钠浸提的腐植酸。红外光谱结果表明,两种提取剂提取的土壤腐植酸均含有大量的芳香化合物和碳水化合物。综上,两种提取剂对土壤腐植酸在热性质及官能团的组成上存在着差异性。  相似文献   

10.
四川成都经济区土壤腐殖质重金属元素含量特征研究   总被引:3,自引:1,他引:2  
通过对四川成都经济区16件土壤样品腐殖质组成及其各组分中重金属元素含量的分析表明,胡敏素是土壤腐殖质的主要组成部分,富里酸和胡敏酸次之。土壤腐殖质中重金属元素含量占土壤全量20%~44%,是土壤重金属污染元素主要存在方式。重金属元素在腐殖质不同组分中的含量具有很大的差异,Cr主要赋存在胡敏素中,Cd、As、Cu、Zn等元素主要赋存在富里酸中。各重金属元素在腐殖酸中含量较高,富里酸中的含量均大于胡敏酸,其机理是富里酸对重金属元素的络合是腐殖酸与重金属相互作用的主要方式。  相似文献   

11.
Interactions between soil humic substances and metal ions I. Isolation and characterization of the soil humic substances From two horizons of a podzol humic acids and fulvic acids were isolated by two different methods. The obtained samples were characterized by elemental analysis, the determination of the ash and moisture content, functional group analysis as well as FTIR-, 1H-NMR-, and 13C-NMR-spectroscopic examinations. In spite of the different isolation methods humic and fulvic acids show great similarities. A higher oxidized state and a lower content of aromatic structural features are clearly observed in the fulvic acids in contrast to humic acids. Besides aromatic structural elements, distinct aliphatic sections were detected in the investigated samples, which showed a lower concentration in the less transformed fractions of the Ahe-horizon.  相似文献   

12.
The sorption of naphthalene and naphthol from water solutions by peat, chernozem, and humic and fulvic acids was studied. The sorption isotherms of naphthalene and naphthol by chernozem corresponded to the Langmuir isotherms. More complex nonlinear isotherms were obtained for peat. Binding of naphthalene and naphthol by humic and fulvic acids can proceed through hydrophobic interactions with aromatic fragments of humic substances and hydrogen bonds between the polar groups of humic molecules and naphthol OH groups.  相似文献   

13.
Experiments were conducted in growth chambers of the Phytotron to evaluate the effects of humic and fulvic acids on growth and ion uptake by tobacco plants grown to flowering.

When small amounts of humic or fulvic acids were added to media used to grow seedlings, the dry weight of roots and tops and the height of the plants subsequently grown in a nutrient solution with small amounts of humic or fulvic acids increased, while at high rates of humic acids they decreased. Generally, there was a trend for low rates of humic acids to increase concentration of Ca and Mg in roots and leaves and to decrease Fe concentration in roots.

The total content of N, K, P, Ca, Mg and Fe in the stalk and leaves increased in the presence of small amounts of humic or fulvic acids in the nutrient solution. Low rates of humic or fulvic acids in the growth medium facilitated the adsorption of Ca, Mg and Fe and their translocation within the plant. For high rates of humic acids there was a trend to decrease the total content of N, K, P, Ca and Fe in the roots and leaves of the plant.  相似文献   

14.
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   

15.
Data were analyzed on the elemental composition of humic and fulvic acids isolated from organic and mineral horizons of different-aged podzols developed on sand quarry dumps in Leningrad oblast. It was shown that the humic substances from the young podzols significantly differed from those isolated from the mature soils. The humic acids (HAs) of the young podzols composed a more homogeneous group of natural compounds compared to the fulvic acids (FAs). The HAs isolated from the organic, podzolic, and illuvial horizons of the embryopodzols significantly differed in their structure. The litter HAs were characterized by the minimum aromaticity and the maximum content of aliphatic components. The HAs from the illuvial horizons contained the maximum portion of aromatic components; a significant portion of carboxyls, ethers, polysaccharides, carbohydrates, and amino acids; and the minimum portion of aliphatic components. The HAs from the podzolic horizons occupied an intermediate position between the humic substances of the organic and illuvial horizons. It was shown that Mendeleev’s formula was more suitable than Aliev’s formula for calculating the calorific values of the HAs because of their structural features. Based on the particular features of the humic substances studied, they were classified as prohumic substances.  相似文献   

16.
Sorption on the mineral matrix is an important process restricting the movement of dissolved organic matter (DOM) in soils. In this study, we aimed to identify the chemical structures responsible for the retention of DOM by sorption experiments with total DOM and acidic humic substances (AHS), containing humic and fulvic acids, on soil samples and minerals (goethite, ferrihydrite, and amorphous Al(OH)3). The AHS remaining in solution after sorption were studied by 13C nuclear magnetic resonance (NMR) analysis, and total DOM and AHS for bed on the surfaces of minerals by diffuse reflectance Fourier-transform infrared (DRIFT) spectroscopy. The soil samples were taken from strongly sorbing Bw horizons of two Inceptisols rich in pedogenetic Fe (29 and 35 g kg ?1) and containing little C (7 and 22 g kg?1). The 13C-NMR spectra showed that sorption causes a preferential removal of aromatic and carboxyl C from the solution, whereas alkyl-C accumulates in the solution. No change was observed for O-alkyl C. The DRIFT spectra of sorbed total DOM and AHS showed a relative increase of the band intensity of carboxyl groups compared to DOM in the initial solution, confirming the importance of those groups for the sorption to mineral surfaces. The spectra also indicated reactions of carboxyl groups with metals at the mineral surfaces. The extent to which the carboxyl groups are bound depended on the surface coverage with DOM and the type of mineral.  相似文献   

17.
Humic substances play a key role in the global carbon cycling and the sequestration of micropollutants in soil. The transformation of these substances by earthworms, the dominant soil macroinvertebrates of many terrestrial ecosystems, and the mechanisms involved are still obscure. We prepared two chemically identical humic model compounds that were specifically 14C-labeled either in the aromatic or the proteinaceous component, and added them to soil incubated with the geophagous earthworm species Metaphire guillelmi (anecic) and Amynthas corrugatus (endogeic). In the absence of the earthworms, both the aromatic and the proteinaceous components were mineralized at similarly low rates (5−8% after 9 days of incubation). In the presence of the earthworms, mineralization rate of the proteinaceous component was strongly stimulated (2-fold by M. guillelmi and 1.4-fold by A. corrugatus). The mineralization rate of the aromatic component was (slightly) stimulated (1.2-fold; P < 0.05) only by A. corrugatus. In all cases, the stimulated mineralization was accompanied by a transformation of radiolabeled humic acids to fulvic acids within the earthworm guts and by an incorporation of radiolabel into the earthworm tissues. Digestion of the proteinaceous component of humic acids by the earthworms was corroborated also by a decrease of extractable humic acids in fresh cast and a stimulated mineralization of soil nitrogen; in the case of M. guillelmi, the fresh cast contained sixfold more NH4+ than the non-ingested soil. Our study provides direct evidence for the selective digestion of humic components by earthworms. Considering the ubiquity of geophagous earthworms and their large biomass, the alteration of the chemical structure of humic substances by the earthworms through their selective digestion of peptidic components may have significant impacts on the stability of humic substances and the bioavailability of micropollutants in soil.  相似文献   

18.
Chromatographic distinction of humic and non humic substances in chernozem-humus Fulvic acids, brown humic acids and grey humic acids from a chernozem from the Austrian Marchfeld were analyzed chromatographically on controlled pore glass with pore diameters of 177 and 259 Å. Concentration of coloured material and concentration of carbon were recorded in the chromatogramms. Specific extinctions at 400 nm were calculated for unit of C and maximal values were taken as constants specific for “pure” humic substances. These were 445,6 ± 10,5,388,7 ± 19,3 and 128,9 ± 0,8 for “pure” grey humic acids, brown humic acids and fulvic acids, respectively. With the aid of these constants, “pure” humic substances could be distinguished from accompanying non humic substances. “Pure” humic substances amounted to 63%, non humic substances to 37% of extractable organic C. 53%, 22% and 25% of the carbon of “pure” humic substances were from grey humic acids, brown humic acids and fulvic acids, respectively.  相似文献   

19.
Degradation of humic substances by soil microorganisms — a review Humic substances which represent differently extractable fractions of the soil organic matter exert multifarious effects on soil as a site for plant growth and a part of terrestrial environments. Among them especially humic acids and fulvic acids are subject to degradation and/or transformation by soil microorganisms. Several authors demonstrated the participation of different species of fungi, actinomycetes and also of non-mycelial aerobic or anaerobic bacteria in those processes under laboratory conditions. Indications exist that humic substances irrespective of their structure undergo degradation on cell surfaces due to the activity of exoenzymes. In this respect microbial phenoloxidases play an extraordinarily important role. The degradation rate of humic substances can be followed by optical, gravimetric and chemoanalytical methods as well as using biochemical and microbiological procedures (CO2 release, microbial growth, biomass formation). An objective evaluation, however, can be hindered by the adsorption of humic substances on microbial biomass and sometimes also by formation of novel humic-like microbial metabolites. Therefore it is necessary to apply a multifactorial approach in the study of the degradation of humic substances which includes both quantitative and qualitative parameters. To better elucidate how these processes may occur under natural conditions, mixed populations of soil microorganisms should be predominantly involved in future studies.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号