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1.
Treatment of acid mine drainage (AMD) highly rich in sulfate and multiple metal elements has been investigated in a continuous flow column experiment using organic and inorganic reactive media. Treatment substrates that composed of spent mushroom compost (SMC), limestone, activated sludge and woodchips were incorporated into bacterial sulfate reduction (BSR) treatment for AMD. SMC greatly assisted the removals of sulfate and metals and acted as essential carbon source for sulfate-reducing bacteria (SRB). Alkalinity produced by dissolution of limestone and metabolism of SRB has provided acidity neutralization capacity for AMD where pH was maintained at neutral state, thus aiding the removal of sulfate. Fe, Pb, Cu, Zn and Al were effectively removed (87–100%); however, Mn was not successfully removed despite initial Mn reduction during early phase due to interference with Fe. The first half of the treatment was an essential phase for removal of most metals where contaminants were primarily removed by the BSR in addition to carbonate dissolution function. The importance of BSR in the presence of organic materials was also supported by metal fraction analysis that primary metal accumulation occurs mainly through metal adsorption onto the organic matter, e.g., as sulfides and onto Fe/Mn oxides surfaces.  相似文献   

2.
Spent mushroom compost (SMC) is commonly used as a carbon source for passive treatment systems in South Korea; however, it has some drawbacks, such as sulfate release from itself. Consequently, investigations to identify effective substitutes for SMC are necessary. In this study, batch experiments were conducted for 27 days to evaluate the efficiency of rice wine waste (RWW) for reducing sulfate and removing dissolved metals within synthetic acid mine drainage (AMD). The results showed that RWW could be more suitable than SMC, which even released sulfate in the early stage of the experiment, for sulfate reduction by sulfate-reducing bacteria. Both materials produced similar results with respect to the removal of dissolved metals, such as Fe and Al. Furthermore, a mixture of SMC and RWW showed the greatest efficiency in sulfate removal. Overall, both RWW and the mixed carbon source showed comparable performance to SMC, which indicated that RWW had a great potential for use as a carbon source for AMD treatment.  相似文献   

3.
Field experiments were conducted over a 460-day period to assess the efficiency of different mixtures of organic substrates to remediate coalmine-generated acid mine drainage (AMD). Five pilot-scale, flow-through bioreactors containing mixtures of herbaceous and woody organic substrates along with one control reactor containing only limestone were constructed at the Tab-Simco site and exposed to AMD in situ. Tab-Simco is an abandoned coal mine near Carbondale, Illinois that produces AMD with pH ∼2.5 and notably high average concentrations of SO4 (5050 mg/L), Fe (950 mg/L), Al (200 mg/L), and Mn (44 mg/L). Results showed that the sequestration of SO4 and metals was achieved in all reactors; however, the presence and type of organic carbon matrix impacted the overall system dynamics and the AMD remediation efficiency. All organic substrate-based reactors established communities of sulfate reducing microorganisms that contributed to enhanced removal of SO4, Fe, and trace metals (i.e., Cu, Cd, Zn, Ni) via microbially-mediated reduction followed by precipitation of insoluble sulfides. Additional mechanisms of contaminant removal were active in all reactors and included Al- and Fe-rich phase precipitation and contaminant surface sorption on available organic and inorganic substrates. The organic substrate-based reactors removed more SO4, Fe, and Al than the limestone-only control reactor, which achieved an average removal of ∼19 mol% SO4, ∼49 mol% Fe, 36 mol% Al, and 2 mol% Mn. In the organic substrate-based reactors, increasing herbaceous content correlated with increased removal efficiency of SO4 (26–35 mol%), Fe (36–62 mol%), Al (78–83 mol%), Mn (2–6 mol%), Ni (64–81 mol%), Zn (88–95 mol%), Cu (72–85 mol%), and Cd (90–92 mol%), while the diversity of the intrinsic microbial community remained relatively unchanged. The extrapolation of these results to the full-scale Tab-Simco treatment system indicated that, over the course of a 460-day period, the predominantly herbaceous bioreactors could remove up to 92,500 kg SO4, 30,000 kg Fe, 8,950 kg Al, and 167 kg Mn, which represents a 18.3 wt%, 36.8 wt%, 4.1 wt% and 82.3 wt% increase in SO4, Fe, Al, and Mn, respectively, removal efficiency compared to the predominantly ligneous bioreactors.The results imply that anaerobic organic substrate bioreactors are promising technologies for remediation of coal-generated AMD and that increasing herbaceous content in the organic substrate matrix can enhance contaminant sequestration. However, in order to improve the remediation capacity, future designs must optimize not only the organic carbon substrate but also include a pretreatment phase in which the bulk of dissolved Fe/Al-species are removed from the influent AMD prior to entering the bioreactor because of 1) seasonal variations in temperature and redox gradients could induce dissolution of the previously formed redox sensitive compounds, and 2) microbially-mediated sulfate reduction activity may be inhibited by the excessive precipitation of Al- and Fe-rich phases.  相似文献   

4.
利用厌氧微生物分离技术,对深度为1.2 m 的海南红树林湿地沉积物钻孔样品进行了分离培养,共获得11 株 厌氧sulfate-reducing bacteria（SRB） 菌株。经显微观察和16S rDNA序列分析,可归纳为6个属,其中已经报道有芽孢杆菌 属（Bacillus）、弧菌属（Vibrio） 和梭状芽胞杆菌属（Clostridium）,另外3个属分别为伯克霍尔德菌属（Burkholderia）、希瓦氏菌属（Shewanella） 和海杆菌属（Marinobacterium）。不同属的细菌对硫酸盐还原的速率最低为14.71%,最高可达 56.78%,并且以上6属11株菌都能将+6价的硫还原生成-2价硫,并与培养基中的Fe2+结合生成黑色FeS沉淀,而这些无定 形FeS沉淀是生成黄铁矿的前体。红树林湿地SRB种群数量随沉积物深度的增加而降低,结合沉积物的地球化学分析测试 结果表明,表层（0 cm） 水界面的沉积物由于处于氧化-还原界面,氧气的周期性输入在一定程度上抑制了SRB的生长;随着 深度增加（10~40 cm）,充足的有机质、偏中性的pH值以及厌氧环境的增强,使得SRB种类和数量明显增加;而60 cm以下 沉积物中因TOC含量降低,减少了微生物可利用的碳源,pH值明显降低,Na+和Ca2+离子浓度明显增加,这些因素都抑制了 SRB的生长,使得深部沉积物中SRB的种类和数量显著减少。  相似文献   

5.
Extracellular enzymatic hydrolysis of high-molecular weight organic matter is the initial step in sedimentary organic carbon degradation and is often regarded as the rate-limiting step. Temperature effects on enzyme activities may therefore exert an indirect control on carbon mineralization. We explored the temperature sensitivity of enzymatic hydrolysis and its connection to subsequent steps in anoxic organic carbon degradation in long-term incubations of sediments from the Arctic and the North Sea. These sediments were incubated under anaerobic conditions for 24 months at temperatures of 0, 10, and 20 °C. The short-term temperature response of the active microbial community was tested in temperature gradient block incubations. The temperature optimum of extracellular enzymatic hydrolysis, as measured with a polysaccharide (chondroitin sulfate), differed between Arctic and temperate habitats by about 8-13 °C in fresh sediments and in sediments incubated for 24 months. In both Arctic and temperate sediments, the temperature response of chondroitin sulfate hydrolysis was initially similar to that of sulfate reduction. After 24 months, however, hydrolysis outpaced sulfate reduction rates, as demonstrated by increased concentrations of dissolved organic carbon (DOC) and total dissolved carbohydrates. This effect was stronger at higher incubation temperatures, particularly in the Arctic sediments. In all experiments, concentrations of volatile fatty acids (VFA) were low, indicating tight coupling between VFA production and consumption. Together, these data indicate that long-term incubation at elevated temperatures led to increased decoupling of hydrolytic DOC production relative to fermentation. Temperature increases in marine sedimentary environments may thus significantly affect the downstream carbon mineralization and lead to the increased formation of refractory DOC.  相似文献   

6.
Under stagnant conditions, the ability of 15 earth materials (non-lime) including various inorganic 2:1 and 1:1 layer silicates, an amorphous oxide, and two 'whole' soils were tested for their pH-buffering efficiency in an acid mine drainage (AMD) water. The purpose was to decrease AMD acidity to a level where sulfate-reducing bacteria (SRB) placed in it may be activated. Of all materials, a whole soil (a high cation-exchange capacity clayey mollisol containing 40% clay, and 4% soil organic matter) caused the greatest pH increases from 2.5 up to 5.5 units after 10 days in the AMD water. Influent AMD was then ameliorated at various speeds through an SRB driven bioreactor using a 50/50 weight over weight (w/w) combination of the mollisol and ryegrass (MR) as the pH buffer substrate. This substrate combination decreased the SRB acclimatisation period (from 50 days in a previous experiment utilising sludge + ryegrass) to <10 days in the present experiment. After causing pH increases from 2.8 to >6 units in 5 days, the buffer reduced the hydraulic retention time (HRT) of the constant-flow reactor from 12 days at flow speeds of 100 ml/day to 2 days at 25 ml/day, respectively. After 10 days, soluble Fe, Al and sulfate were all decreased >1,800-, >40- and 3-fold, respectively. This was a more efficient performance than the no-flow bioreactor of a previous experiment using sludge + ryegrass. This method of AMD rehabilitation is an alternative for localities that lack cheap sources of calcium compounds for chemical treatment, but have a similar soil type and copious quantities of fresh decomposable plant wastes.  相似文献   

7.
The flood zone of the Ob River, the largest (in watershed area) river of the Arctic Ocean basin, is tens of km wide and, after the Amazon's Varzea, is the world's second largest flooding territory. To better understand the biogeochemistry of the Ob River and adjacent surface waters, we studied, in May and July 2014, the dissolved and colloidal organic carbon and trace metals in small rivers, lakes, and flooded water bodies connected and disconnected with the mainstream as well as the Ob River itself. All major and trace elements were distributed among two major categories depending on their pattern of dependence on the dissolved organic carbon (DOC) concentration. Dissolved inorganic carbon (DIC), Na, Mg, Ca, sulfate, Sr, Mo, Sb and U exhibited a general decrease in concentration with the increase of the [DOC]. The lowest concentration of these elements was observed in DOC-rich humic, acidic (4.9 ≤ pH ≤ 6.1) upland lakes fed by surrounding bogs. These elements marked the influence of underground feeding in July during summer baseflow, which was most visible in flood lakes in the Ob riparian zone and the Ob River itself. In May, the flood lakes were statistically similar to the Ob River. The elevated concentration of DOC (up to 60 mg/L) in the upland lakes was not correlated with groundwater-related elements, suggesting a lack of significant groundwater feeding in these lakes. In contrast, insoluble, usually low mobile elements (Al, Fe, other trivalent hydrolysates, Ti, Zr, Hf) and some metals (Cr, Zn, Ni, Pb) demonstrated a steady increase in concentration with increasing DOC, with the lowest values observed in the Ob River and the highest values observed in small tributaries and organic-rich upland lakes in July. It follows that these elements are limited by their main carriers – organic and organo-ferric colloids, rather than by the availability of the source, peat and mineral soil or plant litter. While for the majority of non-colloidal, groundwater-fed elements with high mobility (DIC, Na, Mg, Ca, K, Sr…) the small tributaries can be used as representatives of the Ob main stream, this is not the case for low mobility “insoluble” elements, such as Fe, Al, trivalent and tetravalent hydrolysates, and metal micronutrients (Cu, Zn, and Mn). The low soluble elements and divalent metals exhibited a much lower concentration in the river mainstream compared to that in the flood lakes, upland lakes and small rivers. This difference is significantly more pronounced in the baseflow in July compared to the spring flood in May. Presumably, autochthonous processes, such as the photo-oxidation and bio-oxidation of organo-ferric colloids and phytoplankton uptake are capable decreasing the concentration of these elements in the river mainstream.  相似文献   

8.
Biogeochemical processes involving acetate in sub-seafloor sediments from piston core PC23B from the Bering Sea shelf break were inferred by examining the stable carbon isotopic relationships between acetate and other relevant carbon compounds: total organic carbon (TOC) in the sediment solid phase, and dissolved organic carbon (DOC) and dissolved inorganic carbon (DIC) in pore water. Throughout the core, the isotopic composition of acetate (δ13Cacetate), from −31‰ to −29‰, was 13C-depleted by ca. 7‰ vs. DOC (δ13CDOC) and its depth profile approximately paralleled that of δ13CDOC, suggesting that the principal process producing acetate was fermentation of dissolved organic compounds. However, the 13C depletion in δ13Cacetate indicates some contribution of acetogenesis to total acetate production, because acetogenesis results in 13C depletion of the acetate produced. The relative contribution of acetogenesis via the H2/CO2 reaction, calculated by using a two source isotope mixing model, increased with depth in the sulfate reduction zone from 10% to 15% and was constant at 19% in the methanogenic zone. The acetogenic contribution to acetate production in the methanogenic zone underlying the sulfate reduction zone is consistent with reported observations, whereas the occurrence of acetogenesis in the sulfate reduction zone may be related to the contribution of terrestrial organic matter (OM) to the sedimentary OM in that depth interval, because the terrestrial component likely includes precursors that favor organoautotrophic acetogenesis. The high acetate concentration (up to 81 μM) and TOC content (up to 1.4%) at the same depth (<200 cmbsf) suggest that some relationship exists between acetate production rate and TOC content, or that a temperature increase during core storage at room temperature might stimulate acetate-producing microbial activity in the high TOC sediment.  相似文献   

9.
Dissolved (<1 kDa) and colloidal (1 kDa-0.45 μm) size fractions of sulfate, organic carbon (OC), phosphate and 17 metals/metalloids were investigated in the acidic Vörå River and its estuary in Western Finland. In addition, geochemical modelling was used to predict the formation of free ions and complexes in these waters. The sampling was carried out during high-water flow in autumn and in spring when the abundantly occurring acid sulfate (AS) soils in the catchment area are extensively flushed. Based on the high concentrations of sulfate, acidity and several metals, it is clear that the Vörå River and its estuary is strongly affected by AS soils. The high dissolved form of metals limits also the existence of fish and other organisms in this estuary, and certainly also in other similar shallow brackish estuaries elsewhere in the Gulf of Bothnia. However, generally already <20% saline sea water reduces the concentration for OC and several elements (Al, Cu, Cr, Fe, Pb, PO4 and U) by half and c. 20–30% saline sea water is needed to halve concentrations of Cd, Co, Mn, Ni and Zn. Consequently, these elements as well as organic matters were rapidly precipitated in the estuary, even after mixing with fairly small amounts of the alkaline brackish sea water. Aluminium, Cu, Fe and U most likely precipitate together with organic matter closest to the river mouth. Manganese is relatively persistent in solution and, thus, precipitates further down the estuary as Mn oxides, which concomitantly capture Ba, Cd, Co, Cu, Ni and Zn. In the inner estuary, the high contents of Al is as important than Fe in removing PO4 and, thus, also reducing the risk of algae blooms in near coastal areas influenced by AS soils in the Gulf of Bothnia. Moreover, the dispersion of metals far out in the estuary is dependent on hydrological conditions, i.e. with high flows the plume of metal-rich water will spread further out in the estuary. Furthermore, the extensive drainage of the catchment and subsequent artificial enlargement of the river channel during recent decades has not only enabled oxidation of sulfidic sediments, but strongly increased flow peaks that reach further out in the estuary.  相似文献   

10.
Feasibility of using straw as sole substrate for in situ bioremediation of acidic mine drainage (AMD) was studied. The result showed that straw was more suitable than woodchips, which had been successfully used for bioremediating AMD at the source, for establishing bioremediation layer. The sulfate removal rate of rice straw treatment was almost two times higher than that of the woodchips treatment when the initial pH of the synthetic AMD was set to 3.0. Straw treatment may be more efficient at reducing sulfate than woodchips treatment under stressful conditions. The sulfate removal rate of the rice straw treatment increased from 8.67 to 21.77 mg L−1 day−1 when initial pH increased from 1 to 7 while the removal rate of woodchips treatment increased from 3.80 to 11.95 mg L−1 day−1. The sulfate removal rate of the rice straw treatment decreased from 13.93 to 9.91 mg L−1 day−1 when temperature decreased from 25 to 5°C while the removal rate of woodchips treatment decreased from 7.43 to 4.98 mg L−1 day−1. Differences in soluble organic carbon release between rice straw and woodchips led to the differences in bioremediation efficiency. Concentrations of Cu2+ maintained at low level in the column effluent during the whole bioremediation period. Cu2+ was removed by forming sulfide precipitates. Microbial community analysis showed that sulfate reducing bacteria in the bioremediation layer together with microorganisms capable of degrading rice straw caused the bioremediation of AMD. These findings have significant environmental implications in terms of in situ bioremediation of AMD using straw as sole substrate.  相似文献   

11.
长江口盐沼硫酸盐还原菌的分布特征与环境机制   总被引：3，自引：0，他引：3  
陈庆强  唐媛  杨艳  谢冰  吕宝一 《沉积学报》2012,30(6):1088-1098
选择长江口崇明东滩两类植被区（互花米草、土著植被）纵向剖面,根据不同高程部位柱样土壤和植被根际硫酸盐还原菌（SRB）与异养菌的数量,颗粒有机碳（POC）含量与δ13C值,孔隙水Cl-/SO2-   ４摩尔比等,研究盐沼SRB的空间分布特征与机制。自高潮滩向光滩,柱样氧含量降低,SO2-   ４含量增加,导致SRB含量增加,SRB在有机质矿化中的作用增强。高潮滩柱样不同深度层位的异养菌数量明显大于中潮滩和光滩柱样的相应层位,这与由陆向海柱样氧含量及POC含量降低有关。SRB对植被根际环境的变化较敏感,芦苇根际最有利于SRB生长,藨草根际次之;互花米草根际不利于SRB生长,根系分泌物可能对SRB有抑制作用。土壤有机质含量是导致不同纵向剖面相同高程部位柱样之间微生物数量差异的主要因素。同一纵向剖面不同高程部位柱样之间在土壤氧含量与SO2-   ４含量方面的不同,导致这些柱样微生物数量存在差异。盐沼柱样孔隙水Cl-/SO2-４摩尔比总体偏低,多小于19.33,指示有非海源SO2- ４加入。非海源SO2-４的加入掩盖了硫酸盐还原作用对SO2-４的消耗,增加了利用孔隙水Cl-/SO2-４摩尔比定量研究盐沼硫酸盐还原作用强度的难度。柱样中SRB越多,Cl-/SO2-４摩尔比就越大,硫酸盐还原作用就越明显。  相似文献   

12.
Here we report diel (24 h) and seasonal differences in the concentration and stable carbon isotope composition of dissolved inorganic (DIC) and organic carbon (DOC) in the Clark Fork (CFR) and Big Hole (BHR) Rivers of southwestern Montana, USA. In the CFR, DIC concentration decreased during the daytime and increased at night while DOC showed an inverse temporal relationship; increasing in the daytime most likely due to release of organic photosynthates and decreasing overnight due to heterotrophic consumption. The stable isotope composition of DIC (δ13C-DIC) became enriched during the day and depleted over night and the δ13C-DOC displayed the inverse temporal pattern. Additionally, the night time molar rate of decrease in the concentration of DOC was up to two orders of magnitude smaller than the rate of increase in the concentration of DIC indicating that oxidation of DOC was responsible for only a small part of the increase in inorganic carbon. In the BHR, in two successive years (late summer 2006 & 2007), the DIC displayed little diel concentration change, however, the δ13C-DIC did show a more typical diel pattern characteristic of the influences of photosynthesis and respiration indicating that the isotopic composition of DIC can change while the concentration stays relatively constant. During 2006, a sharp night time increase in DOC was measured; opposite to the result observed in the CFR and may be related to the night time increase in flow and pH also observed in that year. This night time increase in DOC, flow, and pH was not observed 1 year later at approximately the same time of year. An in-stream mesocosm chamber used during 2006 showed that the night time increase in pH and DOC did not occur in water that was isolated from upstream or hyporheic contributions. This result suggests that a “pulse” of high DOC and pH water was advected to the sampling site in the BHR in 2006 and a model is proposed to explain this temporal pattern.  相似文献   

13.
高砷地下水中溶解性有机碳和无机碳稳定同位素特征   总被引：1，自引：0，他引：1  
周殷竹  郭华明  逯海 《现代地质》2015,29(2):252-259
随着稳定同位素分析技术的逐步完善,碳稳定同位素被广泛应用于地球化学领域。高砷地下水砷的生物地球化学循环是目前环境化学研究热点之一。分析概括了碳稳定同位素应用于地下水领域的研究现状,介绍了地下水中有机碳和无机碳稳定同位素的前处理方法以及测试技术。在此基础上,选取了内蒙古河套平原具有代表性的高砷地下水进行氧化还原敏感组分、碳稳定同位素的测定与分析。结果表明,As分布极不均匀,其含量为1.24~387 μg/L。地下水溶解性有机碳(DOC)含量相对较高,与溶解性无机碳(DIC)浓度基本呈正相关。δ13CDIC相对δ13CDOC较富集13C;δ13CDIC-δ13CDOC与δ13CDIC之间具有显著的正相关关系;表明δ13CDIC值越贫化,δ13CDIC-δ13CDOC越小,地下水中来源于有机物氧化分解的无机碳越多,进一步说明有机碳的氧化分解在无机碳稳定同位素贫化过程中起主要作用。此外,δ13CDIC-δ13CDOC与As浓度呈一定的负相关关系;表明有机物的微生物降解对砷的富集具有明显的促进作用。微生物可利用的碳源增加,促进异养微生物的代谢,并消耗氧气,最终形成有利于地下水As富集的还原环境。  相似文献   

14.
The distributions of dissolved organic carbon (DOC) and the natural carbon isotope ratio of DOC (DO13C) in estuaries reflect the predominant sources and sinks of organic matter from both allochthonous and autochthonous origins. The traditional view is that DOC in land-margin ecosystems reflects mainly the mixing of land-derived and oceanic DOC. However, this view is not consistent with the bulk of our data from a survey of DOC and DO13C distributions in estuaries on the East and Gulf coasts of the USA. While it is accurate that the DOC in estuaries includes material derived from land and from the ocean, the distributions of DOC and DO13C in several estuaries reflect additional DOC inputs from estuarine phytoplankton and tidal marshes. Even when DOC concentrations were distributed conservatively, the isotopic composition of the DOC revealed the existence of a dynamic cycle of DOC input and removal in some systems.  相似文献   

15.
Organic matter is an important factor that cannot be neglected when considering global carbon cycle. New data including organic matter geochemistry at the small watershed scale are needed to elaborate more constrained carbon cycle and climatic models. The objectives are to estimate the DOC and DIC yields exported from small tropical watersheds and to give strong constraints on the carbon hydrodynamic of these systems. To answer these questions, we have studied the geochemistry of eleven small watersheds around Basse-Terre volcanic Island in the French West Indies during different hydrological regimes from 2006 to 2008 (i.e. low water level versus floods). We propose a complete set of carbon measurements, including DOC and DIC concentrations, δ13C data, and less commonly, some spectroscopic indicators of the nature of organic matter. The DOC/DIC ratio varies between 0.07 and 0.30 in low water level and between 0.25 and 1.97 during floods, indicating that organic matter is mainly exported during flood events. On the light of the isotopic composition of DOC, ranging from ? 32.8 to ? 26.2‰ during low water level and from ? 30.1 to ? 27.2‰ during floods, we demonstrate that export of organic carbon is mainly controlled by perennial saprolite groundwaters, except for flood events during which rivers are also strongly influenced by soil erosion. The mean annual yields ranged from 2.5 to 5.7 t km? 2 year? 1 for the DOC and from 4.8 to 19.6 t km? 2 year? 1 for the DIC and exhibit a non-linear relationship with slopes of watersheds. The flash floods explain around 60% of the annual DOC flux and between 25 and 45% of the DIC flux, highlighting the important role of these extreme meteorological events on global carbon export in small tropical volcanic islands. From a carbon mass balance point of view the exports of dissolved carbon from small volcanic islands are important and should be included in global organic carbon budgets.  相似文献   

16.
The acid mine drainage (AMD) discharged from the Hejiacun uranium mine in central Hunan (China) was sampled and analyzed using ICP-MS techniques. The analyzing results show that the AMD is characterized by the major ions FeTotal, Mn, Al and Si, and is concentrated with heavy metals and metalloids including Cd, Co, Ni, Zn, U, Cu, Pb, Tl, V, Cr, Se, As and Sb. During the AMD flowing downstream, the dissolved heavy metals were removed from the AMD waters through adsorption onto and co-precipitation with metal-oxhydroxides coated on the streambed. Among these metals, Cd, Co, Ni, Zn, U, Cu, Pb and Tl are negatively correlated to pH values, and positively correlated to major ions Fe, Al, Si, Mn, Mg, Ca and K. The metals/metalloids V, Cr, Se, As and Sb are conservative in the AMD solution, and negatively-correlated to major ions Na, Ca and Mg. Due to the above different behaviors of these chemical elements, the pH-negatively related metals (PM) and the conservative metals (CM) are identified; the PM metals include Cd, Co, Ni, Zn, U, Cu, Pb and Tl, and the CM metals V, Cr, Se, As and Sb. Based on understanding the geochemistry of PM and CM metals in the AMD waters, a new equation: EXT = (Acidity + PM)/pH + CM × pH, is proposed to estimate and evaluate extent of heavy-metal pollution (EXT) of AMD. The evaluation results show that the AMD and surface waters of the mine area have high EXT values, and they could be the potential source of heavy-metal contamination of the surrounding environment. Therefore, it is suggested that both the AMD and surface waters should be treated before they are drained out of the mine district, for which the traditional dilution and neutralization methods can be applied to remove the PM metals from the AMD waters, and new techniques through reducing the pH value of the downstream AMD waters should be developed for removal of the CM metals.  相似文献   

17.
The use of agricultural wastes as biosorbents is gaining importance in bioremediation of heavy metal-polluted water and soils, due to their effectiveness and low cost. This work assesses the Cd, Pb and Cu adsorption capacity of the raw materials used in the production of substrates for mushroom production (Agaricus bisporus and Pleurotus ostreatus) and the spent mushroom composted (SMC), based on the functional groups of their organic carbon. The raw materials studied included agricultural wastes (wheat straw, wheat and rice poultry litter, grape pomace) and inorganic substances (gypsum and calcareous sand). Organic carbon from wastes and their composting products were characterized by CP-MAS 13C NMR. Langmuir adsorption isotherms of metals were plotted for each raw material, composting step, spent A. bisporus and P. ostreatus substrates and the final SMC. The maximum adsorption capacities of SMC were 40.43, 15.16 and 36.2 mg g?1 for Cd, Pb and Cu, respectively. The composting process modified the adsorption properties of raw materials because of the enhanced adsorption of Cd and Cu and decreased adsorption capacity of Pb. CP-MAS 13C NMR and potentiometric titration were used to identify the functional groups of the organic carbon responsible for the metal adsorption. The content of cellulose was correlated with Pb adsorption (p < 0.001), alkyl and carboxyl carbon with Cd adsorption (p < 0.001), and N-alkyl (p < 0.001) and carboxyl (p < 0.010) groups with Cu adsorption. These results are valuable to develop new biosorbents based on agricultural wastes and demonstrate the high potential of SMC to adsorb heavy metals from polluted environments.  相似文献   

18.
Arctic rivers typically transport more than half of their annual amounts of water and suspended sediments during spring floods. In this study, the Sagavanirktok, Kuparuk and Colville rivers in the Alaskan Arctic were sampled during the spring floods of 2001 to determine levels of total suspended solids (TSS) and dissolved and particulate metals and organic carbon. Concentrations of dissolved organic carbon (DOC) increased from 167 to 742 μmol/L during peak discharge in the Sagavanirktok River, at about the same time that river flow increased to maximum levels. Concentrations of dissolved Cu, Pb, Zn and Fe in the Sagavanirktok River followed trends observed for DOC with 3- to 25-fold higher levels at peak flow than during off-peak discharge. Similar patterns were found for the Kuparuk and Colville rivers, where average concentrations of dissolved trace metals and DOC were even higher. These observations are linked to a large pulse of DOC and dissolved metals incorporated into snowmelt from thawing ponds and upper soil layers. In contrast with Cu, Fe, Pb and Zn, concentrations of dissolved Ba did not increase in response to increased discharge of water, TSS and DOC. Concentrations of particulate Cu, Fe, Pb and Zn were more uniform than observed for their respective dissolved species and correlated well with the Al content of the suspended particles. However, concentrations of particulate Al were poorly correlated with particulate organic carbon. Results from this study show that >80% of the suspended sediment and more than one-third of the annual inputs of dissolved Cu, Fe, Pb, Zn and DOC were carried to the coastal Beaufort Sea in 3 and 12 d, respectively, by the Kuparuk and Sagavanirktok rivers.  相似文献   

19.
Tropical small mountainous rivers (SMRs) are increasingly recognized for their role in the global export of dissolved organic carbon (DOC) to the oceans. Here we utilize the Isthmus of Panama as an ideal place to provide first-order estimates of DOC yields across a wide assemblage of bedrock lithologies and land cover practices. Samples for dissolved organic carbon (DOC) analysis were collected across Panama along an E–W transect from the central Panama area to the Costa Rican border for 24 mainstem rivers, 3 large tributary rivers, and one headwater stream. Sampling occurred during both the wet and the dry seasons. DOC concentrations during the wet season are higher than during the dry season in all but three of the rivers. Concentrations vary greatly from river to river and from season to season, with values as low as 0.64 mg l−1 to greater than >25 mg l−1 with the highest concentrations observed for the rivers draining Tertiary marine sedimentary rocks in the Burica and Azuero peninsulas. DOC yields from Panamanian rivers (2.29–7.97 tons/km2/y) are similar to or slightly lower than those determined for other tropical SMR systems. Areas underlain by Tertiary aged sediments exhibited significantly higher mean DOC yields compared to their igneous counterparts, despite maintaining substantially lower aboveground carbon densities, suggesting the important influence of lithology. Finally, regression analyses between DOC yields and select watershed parameters revealed a negative and statistically significant relationship with maximum and mean gradient suggesting lower soil retention times may be linked to lower DOC yields.  相似文献   

20.
Here we report on the temporal changes in the composition of dissolved organic carbon (DOC) collected in the tidal freshwater region of the lower Mississippi River. Lignin-phenols, bulk stable carbon isotopes, compound-specific isotope analyses (CSIA) and 13C nuclear magnetic resonance (NMR) spectrometry were used to examine the composition of high molecular weight dissolved organic matter (HMW DOM) at one station in the lower river over 6 different flow regimes in 1998 and 1999. It was estimated that the annual input of DOC delivered to the Gulf of Mexico from the Mississippi River was of 3.1 × 10−3 Pg, which represents 1.2% of the total global input of DOC from rivers to the ocean. Average DOC and HMW DOC were 489 ±163 and 115 ± 47 μM, respectively. 13C-NMR spectra revealed considerably more aliphatic structures than aromatic carbons in HMW DOC. Lignin phenols were significantly 13C-depleted with respect to bulk HMW DOM indicating that C4 grass inputs to the HMW DOM were not significant. It is speculated that C4 organic matter in the river is not being converted (via microbial decay) to HMW DOM as readily as C3 organic matter is, because of the association of C4 organic matter with finer sediments. The predominantly aliphatic 13C NMR signature of HMW DOM suggests that autochthonous production in the river may be more important as a source of DOC than previously thought. Increases in nutrient loading and decreases in the suspended load (because of dams) in the Mississippi River, as well as other large rivers around the world, has resulted in significant changes in the sources and overall cycling of riverine DOC.  相似文献   

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