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1.
The properties and transformation of dissolved organic matter (DOM) extracted (10 L water per kilogram compost) from municipal solid waste (MSW) compost at five stages (days 47, 77, 105, 126, and 187) of composting were investigated. The DOM was fractionated into hydrophobic or hydrophilic neutrals, acids, and bases. The unfractionated DOM, the hydrophobic acids and neutrals (HoA and HoN, respectively), and the hydrophilic neutrals (HiN) fractions were studied using solid-state 13C-NMR, FTIR, and DRIFT spectroscopy. The HoA fraction was found to be the dominant (percentage of total DOM) hydrophobic fraction, exhibiting a moderate increase during composting. The HoN fraction increased sharply from less than 1% to 18% of the total DOM during 187 days of composting, while the hydrophobic bases (HoB) exhibited the opposite trend. The HiN represented the major fraction of the hydrophiles up to 120 days of composting, decreasing thereafter by 38%. The relative concentration of the hydrophilic acids and bases (HiA and HiB, respectively) exhibited no consistent trend during composting. DRIFT spectra of the unfractionated DOM taken from the composting MSW revealed a decreasing level of polysaccharide structures with time. The 13C-NMR and FTIR spectra of the HoA fraction exhibited a polyphenol-humic structure, whereas the HoN spectra exhibited strong aliphatic features. The spectra of the HiN fraction confirmed its polysaccharide nature. During the final stage of composting, the DOM concentration was steady, while a relative decrease of HiN concomitant with an increase of HoA and HoN fractions was observed. These indicate that the DOM contained a low concentration of biodegradable organic matter and a higher content of macromolecules related to humic substances. The biological significance and heavy metal binding of these fractions are being studied based on earlier observations showing enhanced plant growth in the presence of DOM extracted from mature as opposed to immature compost. 相似文献
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Stefania Mazzuoli Steven Loiselle Vincent Hull Luca Bracchini Claudio Rossi 《洁净——土壤、空气、水》2003,31(6):461-468
The spatial and temporal distribution of humic substances in aquatic ecosystems can have important effects on ecosystem productivity, negatively impacting primary productivity while positively impacting secondary productivity. In the present investigation, a large shallow lake ecosystem was studied to determine the spatial and seasonal variation of the composition and concentration of humic substances. Concentrations of total dissolved organic matter, humic acid, and fulvic acid were found to display significant spatial distributions (1.3…13.5 mg/L, DOM; 0.1…5.4 mg/L, HA). The distribution is described by using mapping techniques and the analysis of the spatial distribution of the lake. An analysis of the seasonal variations also indicated the dependence of the occurrence of these compounds on meteorological and hydrological conditions. To identify the potential sources of these organic materials, an analysis was made of the ratio of humic and fulvic acid fractions and total DOM. It was found that areas of high DOM concentration coincided with the areas of highest HA percentage of total DOM. Furthermore using the ratio of the normalised concentrations of HA, FA, and residual DOM (< 5000 g/mol) it was found that areas dominated by each are spatially distinct. This confirms the hypothesis that in these shallow lakes, photodegradation and bacterioplankton activity will create a residence time dependent zonation of each component of the total DOM. 相似文献
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为探究富营养化湖泊中自生源可溶有机质(DOM)在泥水界面的吸附行为,以马来眼子菜(Potamogeton malaianus)和铜绿微囊藻(Microcystis aeruginosa)释放的DOM为代表,考察针铁矿对草、藻源DOM中不同组分的吸附特征.三维荧光平行因子分析表明类富里酸组分C1和类胡敏酸组分C4的含量很低,而类蛋白物质(类酪氨酸组分C2和类色氨酸组分C3)分别占草、藻源DOM荧光组成的70%和93%. 2种DOM均可被针铁矿吸附,吸附过程符合伪一级动力学.通过等温线拟合发现针铁矿吸附藻源DOM的非线性更强,饱和吸附量(23.77 mg/g)高于草源DOM(19.10 mg/g).特别地,类蛋白组分呈现非线性吸附,而类腐殖物质的吸附近似线性,且针铁矿对于DOM各荧光组分的吸附量顺序为:C3C2 C4 C1,此非均质吸附特征与DOM组分的初始含量、分子大小、芳香性及有效吸附位点有关.红外光谱证实氨基、羧基和羟基是吸附过程中的重要官能团.因此,草、藻源DOM显著改变了针铁矿表面的有机物质组成,影响湖泊沉积物的生物地球化学行为. 相似文献
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无机阴离子及溶解性有机质对程海化学需氧量测定值的影响 总被引：1，自引：0，他引：1
自2005年以来,程海水体的化学需氧量(COD)持续升高,而生化需氧量(BOD)却维持不变,高锰酸盐指数(COD_(Mn))升高也较缓慢.为研究程海COD持续升高的原因,选取程海水体中具有代表性的无机阴离子(Cl~-、F~-、S~(2-)、HCO_3~-)和溶解性有机质(DOM)中不同浓度的胡敏酸(HA)、富里酸(FA)和商品化腐殖酸(SHA),研究其对COD和COD_(Mn)测定的影响,探讨Cl~-和DOM共同存在下对COD测定的影响.结果表明:程海水体中Cl~-浓度对COD存在显著影响,产生的COD值为5.42 mg/L,S~(2-)、F~-和HCO_3~-对COD影响较小;各离子对COD_(Mn)的影响很小;不同浓度梯度的HA、FA和SHA与COD测定结果呈显著线性相关,氧化1 mg C HA、FA和SHA所产生的COD值分别为2.164、1.964和2.362 mg;氧化1 mg C HA和FA所产生的COD_(Mn)值分别为0.646和0.344 mg;DOM对COD测定值的影响显著大于对COD_(Mn)测定值的影响;且一定浓度Cl~-的存在增强了FA与HA对COD测定的影响.该研究为进一步阐明程海COD逐步升高,COD_(Mn)值缓慢升高的内在原因奠定了基础. 相似文献
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A phenoloxidase-producing fungus – Cladosporium cladosporioides – was isolated from water of a bog lake. At high concentrations of carbon (333 mM) and nitrogen (12 mM), the fungus demonstrated the formation of a laccase and a high ligninolytic activity. After addition of riverine or groundwater humic substances into culture media (ca. 1 mg mL–1), the fungus showed the ability of degrading (utilizing) of about 60% of these substances. However, the exact quantification of the degree of degradation was difficult because of adsorption of humic matter on fungal mycelium. Reisolated humic substances were lower in aromatic and higher in aliphatic structures. A crude enzyme from the C. cladosporioides culture showed only low activity in decolorizing humic substances, whereas decolorization up to 50% was observed when using a laccase preparation from Polyporus versicolor, and especially in the presence of a redox mediator. 相似文献
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Doreen Franke Michael W. Hamilton Susan E. Ziegler 《Aquatic Sciences - Research Across Boundaries》2012,74(4):751-768
Boreal watersheds contain a vast quantity of terrestrially derived dissolved organic matter (DOM) originating from wetland and forest soils, yet variation in the potential for photochemical transformation of boreal aquatic DOM sources remains poorly understood. Laboratory solar radiation exposure experiments were conducted on DOM samples collected in three seasons, across nine sites, representing contrasting catchment composition and watershed position to assess variation in the photochemical lability of boreal DOM source and stable carbon isotopic signature (δ13C) of photomineralized DOM. Dissolved organic carbon (DOC) loss rates during laboratory exposure were lowest in summer, suggesting that DOM may have been more photo-degraded during summer. DOM from upstream portions of forested stream sites and wetland-influenced sites was more photolabile relative to downstream portions and the river DOM, suggesting potential losses in photolabile DOM downstream and in the lower reaches of the watershed. Increased a254:a350 and spectral slope following sample exposure suggest photoproduction of low molecular weight (LMW) CDOM and/or a higher photoreactivity of high molecular weight versus LMW compounds. Photomineralization of nitrogen was regulated by organic nitrogen concentration and resulted in NH4 +-photoproduction rates between 0.01 and 0.3?μM N?h?1 and ecologically significant increases in NH4 + for these waters. The δ13C of the photomineralized DOM was positively correlated to initial DOC concentration and generally lower when initial DOC concentrations were lower, suggesting variation in photomineralized DOM δ13C may be a result of kinetic isotope fractionation. Results from this study demonstrate significant variation in the photochemical lability of boreal watershed sources of DOM. Such variation suggests landscape and environmental change has the potential to alter the biogeochemical role photochemical transformations play in downstream portions of boreal watersheds. 相似文献
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Jung‐Hwan Kwon 《洁净——土壤、空气、水》2012,40(5):472-478
The extractable fraction of aqueous colloidal C60 nanoparticles (nC60) was quantified using a liquid–liquid extraction method in the presence of five types of dissolved organic matter (DOM): Aldrich humic acid (AHA), Suwannee River fulvic acid (SFA), sodium dodecyl sulfate (SDS) micelle, liposomes composed of 1‐palmitoyl‐2‐oleoyl‐sn‐glycero‐3‐phosphocholine (POPC), and bovine serum albumin (BSA). The changes in toluene extractable fraction highly depended on the type and dose of DOM. Whereas an environmentally relevant concentration of AHA, 2–20 mg L?1, was sufficient to reduce the nC60 fraction easily destabilized, much higher dose of fulvic acid was needed to result in the similar degree of stabilization. A big contrast between two types of self‐organized DOM, SDS micelle and POPC liposomes, was observed. Although SDS micelle significantly decreased the toluene extractable fraction of nC60 at the dose greater than its critical micelle concentration, no apparent decrease in toluene extractable fraction was found in the presence of POPC liposomes up to 3000 mg L?1. The toluene extractable fraction of nC60 in the presence of BSA rapidly decreases at lower doses then gradually decreased at higher doses. An equilibrium complexation model was proposed to quantitatively describe the decrease in the extractability of nC60 in the presence of DOM. The observed decrease in the extractability of nC60 was well explained by the model and the complexation of nC60 with DOM was thought to occur close to 1:1 molar ratio except for BSA. The association constants of nC60 with DOM were in the order of BSA, AHA, SFA, and SDS micelle, showing the differences in the affinity to nC60. 相似文献
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A natural decay of plant and animal biomass in aquatic environments results in the release of different simple structured organic substances into water. In our laboratory experiments we investigated whether some of them, e.g., starch or peptone, and also a complex yeast biomass can be transformed into humic-like substances by natural assemblages and some pure cultures of aquatic microorganisms. After a 6 months incubation most of the cultural media enriched with those natural organic substrates turned dark in color and humic-like substances (HS) could be isolated. However, the original substrate organic carbon was mainly mineralized in microbial cultures, and only about 3 % C was converted into HS. Total yields of HS differed in dependence of the individual substrate used (peptone > yeast > starch), the origin of inoculum (river > lake > groundwater), and the incubation temperature (20°C > 10°C). According to their elemental composition, and their spectroscopical and electrophoretic characteristics the microbially formed HS resembled natural aquatic humic matter, but were higher in aliphatic constituents (carbohydrates, peptides) and lower in aromatic structures. HS-like substances were also obtained from pure cultures of a bacterium Bacillus sphaericus and a fungus Cladosporium cladosporioides. The 13C and 15N isotopic contents of the microbially produced HS differed in dependence on the microbial inoculum and the type of organic substrates used, but in general they indicated anabolic processes to be mainly responsible for the humification of the simple organic substrates used in our experiments. 相似文献
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The Conductivity Test — Determining the Membrane-toxic Properties of Substances A new biotest system is introduced which is specific in terms of the measured effect but not in terms of the applied organisms. The system is able to detect the effect of membrane-toxic compounds e.g. detergents, organic solvents, and radical formers. Released into the environment, these substances damage biological membranes and therefore cause ion leakage into a surrounding medium. Ion leakage is taken as a measure for membrane damage and is determined as an increase of the electrical conductivity in the medium (conductivity test). The results presented for the tensides benzalkonium chloride, LAS (linear alkylbenzenesulfonate), and APG (alkylpolyglycoside) demonstrate the capability of the conductivity test to distinguish between the differing toxicological potential of these membrane-toxic substances. In contrast to most of the conventional biotests, the endpoint of the conductivity test is independent of a specific organism. This independence is demonstrated by the results obtained with benzalkonium chloride treatment of Elodea canadensis, Lemna minor, and Salvinia natans. The conductivity test represents a versatile, easy to handle biotest system for the assessment of ecotoxicological effects caused by membrane-toxic substances. 相似文献
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Sediment and seawater samples were taken in a sewage affected channel in Blanca Bay, Argentina. Protein content, ‘humic substances’ and silt-clay percentage were evaluated in the sediments; NH4+, PO43? and ‘dissolved organic matter’ in seawater. A highly significant correlation (r=0.747, n=59) was obtained for the relation between protein and % silt-clay. The ‘humic substances’ distribution depends more on the distance from the outfall than does the protein content, probably because of the important relation of the latter with the sediment particle size. The dissolved components showed a dilution pattern similar to that of a contaminant plume in a moving water mass, reaching normal values at 1700 m from the outfall. 相似文献
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John D. Coates Romy Chakraborty Susan M. O&#x;Connor Claudia Schmidt Jürgen Thieme 《洁净——土壤、空气、水》2001,28(7):420-427
As part of a study on microbial redox alteration of humic substances we investigated the potential effect of this metabolism on the fate of heavy metals and hydrocarbons as a result of conformational alteration of the humic molecular structure due to microbial reduction. Our studies indicate that the microbial reduction of humic acids (HA) results in significant morphological and geochemical alterations. X‐ray microscopy analysis indicate that the conformational structure of the humic colloids is altered as a result of the redox change. In the reduced state, the HA appeared as small dense particles, on reoxidation, large loose aggregates were formed. In addition, spectrofluorometric studies indicated that the binding capacity of the HA for naphthalene was decreased by 10% when the HA was reduced. Similarly, the reduced HA yielded higher surface tension values at all concentrations tested which is indicative of a more hydrophilic and less hydrophobic solute. On reoxidation, the surface tension values reverted back to values similar to those obtained for the untreated oxidized HA. These data indicate that the hydrophobicity of the HA is altered on biological reduction of the HA and that this alteration is reversible. In contrast the reduced HA demonstrated a 15% higher affinity for heavy metals such as divalent cobalt than the oxidized HA. In addition to increasing the binding capacity of HA for heavy metals, the reduction of the HA also decreased the bioavailability and toxicity of bound heavy metals such as chromium. When incubated in the presence of Cr(III) and HA, cells of Escherichia coli grew much more rapidly in the presence of the reduced HA suggesting that the higher metal binding capacity of the reduced humic substances resulted in a removal of the Cr(III) from solution and hence reduced its bioavailability and toxicity. These studies demonstrate that HA redox state and reduction of humic acids by microorganisms can have a significant effect on the molecular morphology and binding constants of HA for heavy metals and hydrocarbons and also directly affects the bioavailability of these compounds in the environment. 相似文献
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Photostability and photolability of dissolved organic matter upon irradiation of natural water samples under simulated sunlight 总被引：2，自引：0，他引：2
Davide Vione Vittorio Lauri Claudio Minero Valter Maurino Mery Malandrino Maria Eugenia Carlotti Romeo-Iulian Olariu Cecilia Arsene 《Aquatic Sciences - Research Across Boundaries》2009,71(1):34-45
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Sorption coefficients measured for PAHs on dissolved humic substances by SPME and FQT were found to be inevitably different and method‐dependent – SPME provides activity‐based and FQT concentration‐based sorption coefficients. Poly(acrylic acid) esters as well‐defined model polymers were used in sorption experiments, leading to the conclusion that short aliphatic chains are more effective in binding PAHs than aromatic moieties. FQT was inappropriate to measure sorption coefficients for the interaction of pyrene with poly(acrylic acid) esters but the experiments revealed a characteristic shift in the fluorescence spectrum. Using pyrene as a probe for the molecular environment in the sorbed state, the observed spectral shift indicated a highly hydrophobic microenvironment. The empirical relationships between lg KDOC and lg KOW were generalized on the basis of a modified Flory‐Huggins concept. Introducing only one sorbent‐specific parameter, the solubility parameter δDOM, the calculation of sorption coefficients became possible for a wide range of HOCs using fundamental data readily available from the literature. Long‐term experiments showed that reactive PAHs (such as acenaphthylene and 9‐methylanthracene) are able to react with HAs under strictly abiotic and anoxic conditions, whereas less reactive PAHs (such as naphthalene and dihydroanthracene) do not form bound residues. The HA reveals two functions in the interaction, behaving as a reaction partner and as a protecting ligand. 相似文献
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Dissolved organic matter (DOM) from riverine and lacustrine water was isolated using a reverse osmosis (RO) system. Solid-state 13C nuclear magnetic resonance (13C NMR) was used to quantitatively evaluate the compositions and constituents of DOM, which are compared with previous investigations on marine DOM. Results indicated that concentration factor (CF) was a key metric controlling yield and sorption of DOM on the RO system. The sorption was likely non-selective, based on the 13C NMR and δ13C analyses. Carbohydrates and lipids accounted for 25.0–41.5% and 30.2–46.3% of the identifiable DOM, followed by proteins (18.2–19.8%) and lignin (7.17–12.8%). The freshwater DOM contained much higher alkyl and aromatic C but lower alkoxyl and carboxyl C than marine DOM. The structural difference was not completely accounted for by using structure of high molecular weight (HMW) DOM, suggesting a size change involved in transformations of DOM during the transport from rivers to oceans. 相似文献
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湖泊生态系统作为自然界重要的碳库,光照强度的变化对于湖泊的碳循环过程可能产生重要的影响.以云南老君山高山湖泊天才湖周边土壤中的腐殖酸作为外源溶解性有机物（DOM）的代表物,通过腐殖酸模拟光降解实验,考察光照强度对外源DOM光降解过程的影响.研究结果表明：腐殖酸光吸收系数a440、465 nm和665 nm波长处吸光度比值E4/E6的下降幅度均为：对照组 < 20 W光照组 < 40 W光照组,a440、E4/E6和光谱斜率SR显著相关,表明紫外辐射使得腐殖酸溶液浓度降低、相对分子量下降,且光照强度越强,腐殖酸的光降解程度越大.通过EEM-PARAFAC模型识别出光降解过程中腐殖酸溶液中含有5种荧光组分：UV类腐殖质（C1）、UVA类腐殖质（C2）、类色氨酸（C3）、UVC类腐殖质（C4）和类络氨酸（C5）.40 W光照组中4种荧光组分的降解程度与降解速率均大于20 W光照组,降解程度均为：C4 > C3 > C2 > C1,降解速率为C2 > C4 > C3 > C1,说明不同的荧光组分对光照强度的响应不同.该研究有助于阐明外源DOM的光降解途径与归趋. 相似文献