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1.
化学需氧量(COD)、五日生化需氧量(BOD_5)及溶解性有机碳(DOC)是指示湖泊水质的重要指标,然而上述指标测定通常耗费大量时间、试剂及人力物力且排放大量有害废液.有色可溶性有机物(CDOM)是溶解性有机物(DOM)中可以强烈吸收光谱中的紫外光和可见光的部分,数据测定耗时短、方便快捷,且样品处理过程环境友好,能在很大程度上反映湖泊水质.本研究基于2016年2、5和8月在太湖均匀布设的32个采样点进行样品采集,运用光谱吸收与三维荧光-平行因子分析(EEMs-PARAFAC)探究太湖CDOM的光谱吸收和荧光组分,探讨CDOM光谱指标对湖泊BOD_5、COD及DOC浓度等湖泊环境质量指标的可替代性.结果表明:(1)运用EEMs-PARAFAC方法解析出3种荧光组分:类腐殖酸C1、类酪氨酸C2和类色氨酸C3.(2) COD和BOD_5和DOC在空间上呈现出相似的分布趋势,不同水期的最高值均出现在竺山湾和梅梁湾,由西北湖区至中部敞水区、东南湖湾递减.(3)在不同水期,COD、BOD_5、DOC浓度和C1组分均表现为丰水期极显著大于枯水期和平水期,a_(254)在丰、平、枯水期间无显著性差异,最大值出现在丰水期;C2与C3组分均在枯水期和平水期极显著大于丰水期.(4)在不同水文时期,COD、BOD_5和DOC浓度均与a_(254)、类腐殖酸C1呈显著正相关,丰水期太湖COD、BOD_5和DOC浓度与CDOM光谱指标的线性相关性要优于枯水期和平水期.(5) CDOM光谱指标在不同水文时期均能很好地替代COD、BOD_5和DOC等作为反映太湖水体中有机物污染程度及湖泊水质的指标.  相似文献   

2.
East Fork Poplar Creek (EFPC) is a mercury (Hg) contaminated creek in east Tennessee, USA. Stream restoration activities included the initiation of a flow management programme in 1996 in which water from a nearby lake was pumped to the head of the creek. We conducted regular water sampling for 2 years along the length of EFPC during active flow management and for 5 years after flow management stopped. Total Hg and total monomethylmercury (MMHg) concentration and flux decreased in the uppermost reaches of EFPC that were closest to the point of water addition. Most water quality parameters, including DOC concentration, remained unchanged after flow management termination. Nevertheless, SUVA254, a measure of dissolved organic matter (DOM) composition, increased and coincided with increased dissolved Hg (HgD) concentration and flux and decreased Hg solid-water partitioning coefficients throughout EFPC. Higher SUVA254 and HgD concentration have potential implications for bioavailability and MMHg production. Total and dissolved MMHg concentrations increased in lower reaches of EFPC after the end of flow management and these increases were most pronounced during spring and early summer when biota are more susceptible to exposure and uptake. A general warming trend in the creek after active flow management ended likely acted in concert with higher HgD concentration to promote higher MMHg concentration. Total and dissolved MMHg concentrations were positively correlated with water temperature above a threshold value of 10°C. Concentration changes for Hg and MMHg could not be accounted for by changes in creek discharge that accompanied the cessation of flow management. In addition to the changing DOM composition in-stream, other watershed-scale factors likely contributed to the observed patterns, as these changes occurred over months rather than instantaneously after flow management stopped. Nevertheless, similar changes in MMHg have not been observed in a tributary to EFPC.  相似文献   

3.
The spatial and diurnal tidal variability of dissolved organic carbon (DOC) concentrations and the composition of dissolved organic matter (DOM), as evaluated by high-temperature catalytic oxidation and excitation–emission matrix combined with parallel factor analysis (EEM–PARAFAC), respectively, were determined in Liverpool Bay. EEM–PARAFAC modeling resulted in six fluorescent components characterized as terrestrial humic-like (two), microbial humic-like (two), and protein-like (two). The spatial distributions of DOC and the four humic-like components were negatively correlated with salinity in the high-salinity waters observed in this study (30.41–33.75), suggesting that terrestrial DOM was conservatively distributed. The spatial patterns of protein-like components were largely different from those of DOC, humic-like components, and chlorophyll a, suggesting that these distributions were the combined result of production and degradation in the bay in addition to river inputs. These findings suggest that the DOM dynamics in Liverpool Bay are strongly controlled by river-dominated allochthonous DOM inputs with some less significant contributions of autochthonous DOM within the bay. In addition, the temporal variations of DOM associated with the diurnal tidal cycles were determined at one inshore (31.34–32.24 salinity) and one offshore (33.64–33.75 salinity) station in the bay. Negative linear relationships between salinity and DOM characteristics, i.e., DOC, humic-like, and protein-like components, were observed at the inshore station. In contrast, no relationship was observed at the offshore station, suggesting that the export of DOM through rivers and possibly tidal flats have a noticeable influence on DOM concentration and composition up to a relatively elevated salinity of around 33 in Liverpool Bay.  相似文献   

4.
Dissolved organic carbon (DOC) is one of the most abundant fractions of organic matter in aquatic systems and plays an important role in the dynamics of aquatic environments, controlling both the penetration and the underwater light radiation climate. DOC can be photodegraded by light, thus facilitating biodegradation, especially in regions where the incidence of solar radiation is high, such as higher altitudes and lower latitudes. This study quantified the photodegradation of dissolved organic material in a natural tropical lake surrounded by native forests (Brazilian Atlantic Forest) through two experiments: i) the first experiment exposed concentrated autochthonous, allochthonous, and lake water to in situ solar radiation; ii) this experiment also exposed the same organic material to artificial UV radiation in an incubator under controlled conditions. The quality and quantity of dissolved organic carbon were measured using indices based on carbon absorbance and fluorescence spectrum. In the in situ experiment, it was observed that the DOC degradation profile of the concentrated allochthonous and autochthonous organic material were distinct from each other in the absorbance indices, and the lake water mostly resembled the latter one. On the other hand, we did not see evidence of any significant difference among treatments in the laboratory experiment. An increase in the SR index and a concomitant decrease in the fluorescence of humic compounds and SUVA254 over time were observed. In both experiments, the amount of degraded organic material over time was low and some possible explanations are discussed.  相似文献   

5.
为探究引黄水源水库——门楼水库平水期和丰水期有色可溶性有机物(CDOM)的组成特征、来源及差异,运用紫外—可见光谱技术(UV-vis)和三维荧光光谱(EEMs)技术,结合平行因子分析法(PARAFAC)分析2022年5月(平水期)和2022年7月(丰水期)有色可溶性有机物含量及组分变化。研究结果表明:PARAFAC识别出2类荧光组分,分别是C1(Ex=355 nm,Em=476 nm,类腐殖质组分)和组分C2(Ex=225 nm,Em=320 nm,类蛋白组分);丰水期CDOM组分荧光强度显著高于平水期。CDOM光谱参数表明,门楼水库水体处于中营养状态,水体CDOM受新生内源和外源输入共同影响,以自生源为主;水库CDOM具有相对分子量小、腐殖化程度较弱的特点。丰水期水库富营养化水平和CDOM相对浓度低于平水期;丰水期CDOM疏水性组分比例和芳香化程度高于平水期。水质理化指标、CDOM组分和光谱参数相关性分析结果表明SUVA260和SUVA280与DOC呈显著负相关,说明紫外—可见光谱参数在一定程度上可以用来估算DOC的浓度;Chl.a浓度作为...  相似文献   

6.
In this study, samples were taken from three contrasting freshwater sources and amended with salt in order to determine the influence of salinity and dissolved organic matter (DOM) composition on DOM recovery via ultrafiltration and solid phase extraction (SPE) with C18 disks. Salt addition caused variable recovery of DOM when using C18 SPE, and ultraviolet–visible spectroscopic characterization of the extracted material showed spectral responses that varied among sample sources. In contrast, increasing sample salinity from 0 to 30 ppt consistently caused a 15–25% reduction in the amount of high molecular weight DOM isolated by ultrafiltration for both dissolved organic carbon (DOC) and chromophoric DOM (CDOM), regardless of DOM composition. We hypothesize that a change in conformation (such as coiling or disaggregation) of DOM molecules occurs in the presence of salt, allowing them to pass through the ultrafiltration membrane and thereby decreasing the DOM retained by ultrafiltration. These results are important because they demonstrate that changes in salinity can influence DOM recovery in estuaries. Interpretation of DOM characteristics along estuarine gradients needs to account for potential artifacts introduced by sample isolation techniques.  相似文献   

7.
In order to better understand the compositional and structural complexity of dissolved organic matter(DOM) macromolecules and provide mechanistic information on the binding of hydrophobic organic contaminants(HOCs) to DOM, we fractionated large amounts of lake water into three hydrophobic DOM-fractions. The variation of the partitioning coef?cients(K_(DOC)) of pyrene at different p H levels was examined by ?orescence quenching titration. Results show that, relative to the more polar acidic DOM-fractions, the hydrophobic neutral fraction exhibits a higher sorption ability to pyrene. Generally, the sorption of pyrene to the three hydrophobic fractions is strongly pH-dependent. The K_(DOC) values of pyrene generally increase with decreasing p H levels, which is especially obvious in the sorption of pyrene to the fulvic acid fractions, suggesting that the binding is controlled by hydrophobic interactions. The mechanisms underlying the binding of pyrene to the hydrophobic fractions were also discussed. Our data are bene?cial to further understanding the binding of HOCs to DOM and how it has been affected,which may result in more accurate predictions of K_(DOC).  相似文献   

8.
The bioavailability of predegraded dissolved organic matter (DOM) from a humic-rich, boreal river to estuarine bacteria from the Baltic Sea was studied in 39-day bioassays. The river waters had been exposed to various degrees of bacterial degradation by storing them between 0 and 465 days in dark prior to the bioassay. The resulting predegraded DOM was inoculated with estuarine bacteria and the subsequent changes in DOM quantity and quality measured. During the incubations, dissolved organic carbon (DOC) and oxygen concentrations decreased, indicating heterotrophic activity. Coloured DOM was degraded less than DOC, indicating a selective utilization of DOM, and humic-like fluorescence components increased during the incubations. The amount of DOC degraded was not affected by the length of DOM predegradation. The percentage of bioavailable DOC (%BDOC) was higher in experiment units with added inorganic nitrogen and phosphorus than without addition (on average 13.5 % and 9.0, respectively), but had no effect on the degradation of fresh, non-predegraded, DOC (%BDOC 12.0 %). Bacterial growth efficiency (BGE) was highest (65 ± 2 %) in the units with fresh DOM, and lowest in units with predegraded DOM and no added inorganic nutrients (11 ± 4 %). The addition of inorganic nutrients increased the BGE of predegraded DOM units by an average of 28 ± 4 %. There was no significant effect on BGE by length of predegradation after the initial drop (<3 months). This study suggests that both the length of predegradation and the inorganic nutrient status in the receiving estuary has consequences to carbon cycling and will determine the amount of terrestrial-derived DOC being ultimately assimilated into marine food webs.  相似文献   

9.
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   

10.
有色溶解性有机物(CDOM)广泛存在于水体中，占溶解有机碳(DOC)10%～90%，其浓度影响水环境碳循环过程、污染物质迁移以及水生生物群落的结构和功能。为分析东北地区水库DOC碳循环情况，本文于2015—2020年对第二松花江流域典型水库白山水库和丰满水库进行5次现场观测和室内实验，在分析CDOM吸收特性的基础上，基于Landsat系列卫星利用波段比值法建立CDOM浓度反演模型(R2=0.82)，根据实测值CDOM与DOC的强相关性(R2=0.78)，进而估算水库DOC浓度。结果表明：(1)利用野外实测数据和Landsat系列卫星能够对东北内陆水库CDOM浓度进行良好反演，(2)2000—2020年白山水库和丰满水库年际CDOM和DOC浓度变化不大，在2010年之后表现出轻微上升趋势，CDOM浓度从支流和干流的汇入到主库区呈现逐渐减少趋势，(3)白山水库和丰满水库M值(CDOM在250和365 nm处吸收系数比值)和S275～295(CDOM在275～295 nm波段处的吸收光谱的斜率)较小、SUVA254<...  相似文献   

11.
Photobleaching of humic rich dissolved organic matter   总被引：7，自引：0，他引：7  
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12.
高邮湖、南四湖和东平湖作为南水北调东线枢纽湖泊,其水质状况对保障调水安全起到关键性作用本文运用三维荧光光谱平行因子分析法(EEMs-PARAFAC)分析了3个湖泊在不同水文情景下有色可溶性有机物(CDOM)吸收、荧光光谱特征以及荧光组分与主要水质参数的相关性,以探究3个湖泊CDOM来源组成特征结果表明,平行因子分析法解析CDOM三维荧光图谱,得到陆源类腐殖质C1、类色氨酸C2和类酪氨酸C3不同水文情景对高邮湖CDOM来源与结构组成影响较明显,丰水期其类腐殖质荧光强度显著大于枯水期(t-test,P0.01),并且与a(254)呈正相关(R~2=0.85,P0.01),表明类腐殖质是CDOM主要部分,该荧光组分贡献率可达50%[F_(max)C1/(F_(max)C1+F_(max)C2+F_(max)C3)×100%],高邮湖受到入湖河流来水的影响较大,丰水期入湖口附近荧光强度明显高于其他水域东平湖和南四湖CDOM来源组成特征相似,丰水期东平湖和南四湖组分C2和C3显著低于枯水期(t-test,P0.01),两湖泊枯水期工农业等人为污染源影响较大相关性分析表明高邮湖中类腐殖质荧光特征在一定程度是能反演DOC浓度,并且类腐殖质的输入会增加湖泊总磷、总氮和叶绿素a浓度而东平湖和南四湖CDOM荧光特征与主要水质参数的相关性较差,这与高邮湖水体存在较大差异.  相似文献   

13.
Changes in molecular size distribution associated with degradation of refractory DOM (macromolecules, apparent mol wt. ≥1500) by 3 strains of bacteria were investigated by Sephadex G-15 gel permeation chromatography and DOC analysis of the eluates. Macromolecules and bacteria were isolated from the same lake water sample, one taken in summer and one in winter. The decompositional changes of the DOM fraction were compared with respect to substance- and bacterial species-specific differences, and with respect to the action of photolysis and co-substrate supplementation. The metabolite patterns resulting from the simultaneous growth of the bacteria on the persistent DOM fraction and the labile co-substrate, glutamic acid were analyzed. The macromolecules differed in accessible components, and the bacteria degraded most effectively the DOM fraction of the parent lake water sample. Photolysis was the prerequisite for the reduction of the inaccessible bulk of the macromolecules. Glutamic acid enhanced the degradation of the macromolecules. The enhancement effect was impaired by the build up of waste products which balanced the losses of the DOM fraction. Three formation modes of refractory metabolites could be distinguished: formation of intensely UV absorbing small sized products which were poor in DOC during degredation of (1) the macromolecules of winter, and (2) of glutamic acid, and formation of (3) apparent high molecular weight substances from glutamic acid in cultures containing the macromolecules of summer which probably results from a stable linkage between the small sized metabolites of the amino acid and the DOM fraction. The research was supported by the Deutsche Forschungsgemeinschaft.  相似文献   

14.
赵紫凡  孙欢  苏雅玲 《湖泊科学》2019,31(4):1088-1098
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   

15.
为了揭示湖库内源性污染物的分布、来源、组成及垂向分布特征,以新建人工深水湖泊龙景湖为研究对象,采用紫外-可见光谱和三维荧光光谱技术,研究了该湖泊以成湖前用途划分的3个特征区域(原河道底部、新淹没区底部和新淹没区边坡)的沉积物上覆水和孔隙水中的溶解性有机质(DOM)的光谱特征.结果表明,孔隙水中的DOM芳香性和腐殖化程度高于上覆水;孔隙水中疏水组分含量大于上覆水,且水体中可能存在内源孔隙水释放的低分子量DOM.龙景湖上覆水和孔隙水中的DOM主要源于水体自身的微生物,自生源特征明显,且可能存在新近释放到水体的有机质.龙景湖沉积物上覆水和孔隙水中的DOM以类腐殖酸和类蛋白质为主,且随着深度增加,类腐殖酸峰强度增强,与龙景湖的建湖背景有明显联系.  相似文献   

16.
An ultrafiltration methodology and the results of its application on Elbe river water are presented. Compared with other methods, Ultrafiltration allows fractionation of the molecular-weight fractions of DOC for higher volumes of solution in a shorter time. To characterize the molecular-weight fractions, the sum parameter DOC (β(DOC)) and the absorption coefficient at 254 nm a254 were measured, together with determination of a254/ β(DOC) for further characterization of the DOC fractions and to provide information about changes in parts of the UV-active substances of the total dissolved organic material. In the period May 1992 to November 1994, the DOC molecular-weight composition of 65 samples of Elbe river water were determined. At two sampling locations (Torgau-East and Meissen), the DOC content β(DOC) was approximately 6 mg/L. The high-molecular weight fraction (> 10000 g/mol) gave a mean of 13% of the total DOC content β0(DOC). The measurements showed that the molecular composition of DOC in the Elbe does not greatly differ. There was also no clear seasonal influence on the molecular-weight composition of the DOC content. During the period of investigation, the percentage part of β(DOC) and a254/β(DOC) of the high-molecular weight fraction of the total dissolved organic material increased, while the a254/β(DOC) values of the middle molecular-weight fraction remained fairly constant. The dependence of β(DOC) on discharge of the Elbe river is low. Changes in molecularweight composition of DOC were only observed during the steepest increase in river discharge during a flood event, with another spectrum of substances responsible for the increase in β(DOC) when compared with the β(DOC) for low or middle water level.  相似文献   

17.
Waterborne carbon (C) export from terrestrial ecosystems is a potentially important flux for the net catchment C balance and links the biogeochemical C cycling of terrestrial ecosystems to their downstream aquatic ecosystems. We have monitored hydrology and stream chemistry over 3 years in ten nested catchments (0.6–15.1 km2) with variable peatland cover (0%–22%) and groundwater influence in subarctic Sweden. Total waterborne C export, including dissolved and particulate organic carbon (DOC and POC) and dissolved inorganic carbon (DIC), ranged between 2.8 and 7.3 g m–2 year–1, representing ~10%–30% of catchment net ecosystem exchange of CO2. Several characteristics of catchment waterborne C export were affected by interacting effects of peatland cover and groundwater influence, including magnitude and timing, partitioning into DOC, POC, and DIC and chemical composition of the exported DOC. Waterborne C export was greater during the wetter years, equivalent to an average change in export of ~2 g m–2 year–1 per 100 mm of precipitation. Wetter years led to a greater relative increase in DIC export than DOC export due to an inferred relative shift in dominance from shallow organic flow pathways to groundwater sources. Indices of DOC composition (SUVA254 and a250/a365) indicated that DOC aromaticity and average molecular weight increased with catchment peatland cover and decreased with increased groundwater influence. Our results provide examples on how waterborne C export and DOC composition might be affected by climate change. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

18.
Dissolved organic matter (DOM) concentration and composition in riverine and stream systems are known to vary with hydrological and productivity cycles over the annual and interannual time scales. Rivers are commonly perceived as homogeneous with respect to DOM concentration and composition, particularly under steady flow conditions over short time periods. However, few studies have evaluated the impact of short term variability (<1 day) on DOM dynamics. This study examined whether diurnal processes measurably altered DOM concentration and composition in the hypereutrophic San Joaquin River (California) during a relatively quiescent period. We evaluated the efficacy of using optical in situ measurements to reveal changes in DOM which may not be evident from bulk dissolved organic carbon (DOC) measurement alone. The in situ optical measurements described in this study clearly showed for the first time diurnal variations in DOM measurements, which have previously been related to both composition and concentration, even though diurnal changes were not well reflected in bulk DOC concentrations. An apparent asynchronous trend of DOM absorbance and chlorophyll‐a in comparison to chromophoric dissolved organic matter (CDOM) fluorescence and spectral slope S290–350 suggests that no one specific CDOM spectrophotometric measurement explains absolutely DOM diurnal variation in this system; the measurement of multiple optical parameters is therefore recommended. The observed diurnal changes in DOM composition, measured by in situ optical instrumentation likely reflect both photochemical and biologically‐mediated processes. The results of this study highlight that short‐term variability in DOM composition may complicate trends for studies aiming to distinguish different DOM sources in riverine systems and emphasizes the importance of sampling specific study sites to be compared at the same time of day. The utilization of in situ optical technology allows short‐term variability in DOM dynamics to be monitored and serves to increase our understanding of its processing and fundamental role in the aquatic environment. Copyright © 2007 John Wiley & Sons, Ltd.  相似文献   

19.
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20.
章奇  居琪  李健欣  曹驰程  江和龙  张晖 《湖泊科学》2020,32(4):1041-1049
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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