水稻子实对不同形态重金属的累积差异及其影响因素分析

在分析成都平原核心区土壤重金属(Cd、Cr、Pb、Cu、Zn)全量、各形态含量及相应点位种植的水稻子实重金属含量的基础上,通过统计分析、空间插值及线性回归方程的模拟,研究了土壤Cd、Cr、Pb、Cu、Zn全量的空间分布状况、各形态重金属含量统计特征,以及水稻子实对重金属各形态的累积差异及其影响因素。结果表明,成都平原水稻土重金属污染较轻,除Cd外,均低于国家土壤环境质量二级标准。土壤中重金属的可交换态含量均较低,Cd主要以铁锰氧化态存在,Cr、Cu、Zn、Pb主要以残渣态存在。水稻子实对5种重金属的累积效应顺序为:Cd>Zn>Cu>Pb>Cr。与水稻重金属累积关系密切的重金属活性形态(可交换态、碳酸盐结合态、铁锰氧化物结合态和有机物结合态)主要有:Cd的碳酸盐结合态、Cr的可交换态、Pb的有机物结合态和Cu的碳酸盐结合态含量;Zn各活性形态对水稻子实含量的影响不明显。土壤理化性质对不同活性形态重金属元素的影响效应各不相同。活性态Cd主要受有机质、pH和容重的影响;活性态Cr与pH、有机质、CEC和容重密切相关;活性态Pb与有机质、容重、中细粉粒、砂粒等均有密切的关系;Cu的活性主要受粘粒、有机质含量的影响;Zn的有效性主要受pH、有机质、砂粒、容重的影响。总的看来,对土壤Cd、Cr、Pb、Cu、Zn各活性形态含量影响效应较强的是有机质、pH、容重,而与土壤吸附性能密切相关的颗粒组成、CEC的影响不甚明显。     

Determination of High Resolution Pore Water Profiles of Trace Metals in Sediments of the Rupel River (Belgium) using Det (Diffusive Equilibrium in Thin Films) and DGT (Diffusive Gradients in Thin Films) Techniques

The techniques of diffusional equilibrium in thin films (DET) and diffusional gradients in thin films (DGT) were used to obtain high resolution pore water profiles of total dissolved and labile trace (mobilizable) metals in the sediments of the Rupel River, Belgium. DGT measures labile metal species in situ by immobilizing them on a resin gel after diffusion through a diffusive gel whereas for DET an equilibrium is established between the DET gel and the pore water. Concentrations of Pb and Zn obtained by DGT were in good agreement with the results obtained by centrifugation, and thus were well buffered by rapid equilibrium with the solid phase, whereas Fe, Mn and Cd were very tightly bound to the sediment phase and large differences were observed between the labile and the total metal concentrations. Cu, Zn, Co and Ni show intermediated behavior. Good correlations were found between the profiles of As and Fe and Mn and Co for DET as well as DGT showing a close link between the geochemical behavior of these elements. Cu, Zn, Pb and Cd are also influenced by the reductive mobilization of Fe and Mn oxides but are also closely linked to the bacterial degradation of organic matter in the surface sediments as to the precipitation of metal sulfides in the deeper layers.     

Laboratory Investigation of the Geochemical Behavior of Metals in Paddy Soils Contaminated with Mine Tailings

The geochemical behavior of metals, including Fe, Mn, Pb and Zn, in contaminated paddy soils was investigated during the cultivation of rice crops through laboratory microcosm experiments. From the two paddy fields contaminated by mine tailings, Siheung and Deokeum in Korea, paddy soils were collected and analyzed for their geochemical characteristics. The Siheung paddy soil showed higher levels of heavy metals, whereas the higher potential for the release of metals was anticipated due to the extremely acidic conditions at Deokeum. In microcosm experiments of flooded paddy soils over 18 weeks, Fe and Mn were released in subsurface pore waters by reductive dissolution, and Pb and Zn were dissolved in high amounts at the surface by oxidation of sulfides. Although amorphous Fe oxide-rich layers were formed at the surface of both paddy soils, the release of Pb and Zn were controlled at the surface by these layers only under slightly alkaline conditions at Siheung. Lead and Zn were associated with the reducible and carbonate fractions at the surface paddy soil of Siheung from the sequential extraction on core samples collected during the flooded period. In the acidic conditions at Deokeum, Pb and Zn were continuously released until the late stage of flooding. A great increase in the exchangeable fraction of metals was observed after the soils had drained. The bioavailability of metals for rice crops would be high under acidic conditions at Deokeum, despite the lower levels of heavy metal contamination.     

Prolonged Testing of Metal Mobility in Mining-Impacted Soils Amended with Phosphate Fertilisers

The aim of the study was to determine whether the application of superphosphate fertiliser to soils contaminated with mine wastes can inhibit metal and metalloid mobility (Cu, Pb, Zn, Cd, Fe, Mn, As, Sb) in the long term. Contaminated soils contained sulfide- and sulfate-rich waste materials from the Broken Hill and Mt Isa mining centres. Results of long-term (10 months) column experiments demonstrate that fertiliser amendment had highly variable effects on the degree of metal and metalloid mobilisation and capture. Rapid release of metals from a sulfate-rich soil showed that phosphate amendment was ineffective in stabilising highly soluble metal-bearing phases. In a sulfide-rich soil with abundant organic matter, complexing of metals with soluble organic acids led to pronounced metal (mainly Cd, Cu and Zn) release from fertiliser-amended soils. The abundance of pyrite, as well as the addition of fertiliser, caused persistent acid production over time, which prevented the formation of insoluble metal phosphate phases and instead fostered an increased mobility of both metals and metalloids (As, Cd, Cu, Sb, Zn). By contrast, fertiliser application to a sulfide-rich soil with low organic carbon content and a sufficient acid buffering capacity to maintain near-neutral pH resulted in the immobilisation of Pb in the form of newly precipitated Pb phosphate phases. Thus, phosphate stabilisation was ineffective in suppressing metal and metalloid mobility from soils that were rich in organic matter, contained abundant pyrite and had a low acid buffering capacity. Phosphate stabilisation appears to be more effective for the in situ treatment of sulfide-rich soils that are distinctly enriched in Pb and contain insignificant concentrations of organic matter and other metals and metalloids.     

PARTITIONING OF HEAVY METALS IN PODZOL SOILS CONTAMINATED BY MINE DRAINAGE WATERS,DALARNA, SWEDEN

The discharge of acidic mine drainage waters onto a hillslope in Dalarna, central Sweden, has lead to the contamination of the podzol soils with Cu, Fe, Ni, Pb, Zn and sulfate. Samples from contaminated and reference soils have been collected for chemical and mineralogical analyses. Jarosite is identified by x-ray diffraction analysis as a precipitate in the upper horizons (A, E, B) of the contaminated soils, where the soil acidity (pH_KCl～2.6) promotes jarosite stability. The sequential chemical extraction of soil samples indicates that, in the reference A horizon, Cu, Pb, Ni and Zn are bound primarily to cation exchange sites and organic matter. In the A horizon of the contaminated soils closest to the rock dump, metal partitioning is dominated by the Fe oxide fractions, despite the high organic matter content; Pb is almost completely bound to crystalline Fe oxides, possibly adsorbed to Fe oxides or occuring in a jarosite solid solution. In the reference B and C horizons, Cu, Ni and Zn are primarily adsorbed/coprecipitated in the Fe oxide fractions, while Pb remains with a large fraction bound to organic matter. In the Fe-rich B horizon of the contaminated soils, the partitioning of the metals in cation exchange sites and to organic matter has greatly increased relative to the reference soils, resulting from the mobilization of organo-metal complexes down the profile.     

Trace metal composition and speciation in street sediment: Sault Ste. Marie,Canada

Street sediment collected in Sault Ste. Marie, Ontario was examined for trace element composition (As, Cd, Cr, Cu, Fe, Pb, Hg, Ni and Zn) and the metal partitioning to various sediment properties was determined by sequential extraction. Total Ni, Cu, Zn and Pb concentrations exceeded the lowest effect levels specified in the Ontario Provincial Sediment Quality Guidelines for Metals (Environment Ontario, 1992) and derived from bioassay studies. According to these Guidelines, the disposal of such sediment has to be guided by environmental considerations. A significant fraction of these metals was extractable in 0.5 N HCl over a 12-hour period and considered as potentially bioavailable. The major accumulative phases of toxic metals in this sediment are exchangeable, carbonate, Fe/Mn oxides and organic matter but the relative importance of each phase varied for individual metals. Approximately 20% of the total extractable Cd is found in each of these four fractions. Pb, Zn and Mn are predominantly bound to carbonates, Fe/Mn oxides and organic matter. Cu shows a high affinity for organic matter and to a lesser extent for carbonates. Elevated levels of Cd, Pb, Cu, Zn, Mn and Cr in the exchangeable and/or soluble phase suggest that sediment associated metals, mobilised from streets in Sault Ste. Marie during runoff and snowmelt, would adversely impact water quality in the receiving waters. However, large fractions of the total metal load are associated with coarser particles which are unlikely to be transported through the drainage system into receiving waters.     

渤海湾各形态重金属的地球化学特征及其环境意义

根据2008年对渤海湾的调查,重点研究了渤海湾湾内和湾口柱状沉积物重金属的生物地球化学特征,通过剖析不同形态重金属的特征,结合渤海湾生态环境信息的综合分析,系统探讨了渤海湾沉积物重金属的演变趋势、影响控制因素以及潜在生态风险。结果表明,湾内海河口附近沉积柱重金属含量有几次突变,20～22cm段极小值可对应1939年海河北系的洪水,10～12cm段极小值可对应1963年海河南系的洪水,1963年至今重金属含量有逐渐增加的趋势。不同形态重金属百分含量从大到小为：残渣态〉铁锰氧化物结合态〉碳酸盐结合态〉有机结合态〉可交换态,且重金属在海河口附近都表现出较高的可浸取态百分含量。风险评价结果表明,重金属总量富集因子由大到小为：Pb〉Cd〉Zn〉Cr〉V〉Co〉Cu〉Ni,其中Pb、Cd和Zn的富集因子均大于1,说明其有污染,但渤海湾沉积物总体质量良好,潜在生态风险较低。从重金属形态角度评价,V和Cr无污染,Zn、Co、Cu、Ni和Pb在湾内及湾外均有不同程度的污染,而Pb的污染最为严重。     

Mikrosondenuntersuchungen an unterschiedlich stark mit Schwermetallen belasteten Böden. 2. Gehalte an Schwermetallen und anderen Elementen in Huminstoffaggregationen,Streustoffen und Holzkohlepartikeln

Electron microprobe studies on soil samples with varying heavy metal contamination. 2. Contents of heavy metals and other elements in aggregations of humic substances, litter residues and charcoal particles EMA point analysis show that the organic matter constituents of heavy metal contaminated soils are highly enriched with heavy metals. The maximal trace element accumulation were for Cu up to 13,000 mg/kg, for Zn up to 48,000 mg/kg, for Cd up to 2,100 mg/kg and for Pb up to 193,000 mg/kg. The affinity for the accumulation of the different heavy metals in aggregations of humic substances can be described by the sequence Cu > Pb ? Cd > Zn ? Ni > Co. In very strongly acidified humic top soil horizons the Pb and Cd accumulation in the organic matter constituents is in competition with the accumulation in Fe and Mn oxides. The heavy metal contents (especially of Cu) of the organic matter are often correlated with the content of organically bound calcium. The EMA results also show that high heavy metal amounts occur in combination with Ca-accumulations in the epidermis and the outer bark parenchym of decayed roots. EMA point analysis of the interior of fungus sclerotias show that sclerotias can contain high amounts of heavy metals, in particular lead (up to 49,700 mg Pb/kg). From statistical results of EMA point analysis follows that lead and other heavy metals attached to humic substances are not only bound as metal organic complexes but also as organic metal phosphate complexes. Also charcoal particles of polluted soils contain high amounts of heay metals. The accumulation affinity is quite similar to that of humic substances.     

Origin,retention and release of trace metals from sediments of the river seine

Metallic contents (Fe, Mn, Pb, Cu, Cd, Zn, Cr) of sediments were measured in 14 sites in the River Seine (France) along 110 km; in three sites surrounding the sewage treatment plant at Achères, vertical profiles were established from cores and dialysis cells, and interface exchanges have been studied. Metal contamination increases downstream, except for Pb for which contamination is higher immediately downstream of stormdrains (up to 130 mg kg^?1); that confirms its urban origin. Upstream of Achères, metallic contamination increases with depth while downstream, contribution to sediments of suspended matter from the treatment plant, loaded with organic matter, alters the behaviour of metals within the first ten centimeters. A strong link between particulate organic carbon (POC), polycyclic aromatic hydrocarbons (PAH), polychlorobiphenyls (PCB) and metal contents has been established. The organic matter brought down by the treatment plant effluents induces a specific diagenesis downstream leading to metal release in summer as attested by a 30% metal contents decrease in sediments. Calculation of molecular diffusion fluxes shows that in september, the release phenomenon is ending.     

Flüssebilanzen und aktuelle Änderungsraten der Schwermetall-Vorräte in Wald-Ökosystemen des Soiling

Flux balances and current rates of change of heavy metal stores in forest ecosystems of the Soiling The inventory of the heavy metals Cr, Mn, Fe, Co, Ni, Cu, Zn, Cd, and Pb is calculated for a beech and a spruce forest ecosystem in the Soiling mountains on the basis of measured concentrations in the vegetation and soil compartments and their dry mass per hectare. The inventory is compared with measured heavy metal fluxes coupled with precipitation above and below the canopy, with seepage water fluxes below the rooting zone (50 cm depth), with litterfall, and with the current increment to biomass. The ratios between heavy metal stores in the forest floor layers (table 3) and the annual flux with litterfall (table 4) show decreasing tendency for liberation of the elements by decomposition of organic matter (OM) in the following order: Mn>OM>Ni>Cd>Cu>Cr ≈? Zn>Co ≈? Fe ≈? Pb Manganese is set free faster than total organic matter. The flux balances for the total ecosystems (table 4) show input > output in the case of Cr, Fe, Cu, Cd, and Pb; input ≈? output for Ni and Zn; input < output for Mn and Co. Heavy metal stores in mineral soil are decreasing by percolation losses and increment to biomass (mainly wood) in the case of all elements investigated, except Zn (under beech), Cd and Pb (table 4). The concentrations of Cu and Pb in the forest floor layers have reached levels at which deleterious effects on microorganisms and litter decomposition are to be expected.     

Treatment of Acid Mine Drainage Using Fly Ash Zeolite

In this paper, two Indian fly ashes (from Talcher and Ramagundam) were converted into zeolites and both the raw fly ash and zeolite were used to treat two British acidic mine waters. The results demonstrate that fly ash zeolites are more effective than raw fly ash for treatment of acid mine drainage. Fly ash has been found effective for removal of Pb, but with increased dosing, caused release of Ba, Cr, Sr (both fly ashes) plus Zn, Ni (Talcher), or Fe (Ramagundam) into mine water. In contrast, increased dosing with fly ash zeolite removed 100% Pb, 98.9% Cd, 98.8% Zn, 85.6% Cu, 82.8% Fe, 48.3% Ni, and 44.8% Ba from mine water. Fly ash is amorphous in nature and many metals attached on the surface of the ash particles are easily leached off when ash comes in contact with acidic mine water. However, fly ash zeolite is crystalline in nature and due to its high cation exchange properties, most of the metals present in acid mine water are retained in surface sites.     

Rhizosphere effects of <Emphasis Type="Italic">Populus euramericana</Emphasis> Dorskamp on the mobility of Zn,Pb and Cd in contaminated technosols

Purpose

This study aimed at investigating the rhizosphere effects of Populus euramericana Dorskamp on the mobility of Zn, Pb and Cd in contaminated technosols from a former smelting site.

Materials and methods

A rhizobox experiment was conducted with poplars, where the plant stem cuttings were grown in contaminated technosols for 2 months under glasshouse conditions. After plant growth, rhizosphere and bulk soil pore water (SPW) were sampled together. SPW properties such as pH, dissolved organic carbon (DOC) and total dissolved concentrations of Zn, Pb and Cd were determined. The concentrations of Zn, Pb and Cd in plant organs were also determined.

Results and discussion

Rhizosphere SPW pH increased for all studied soils by 0.3 to 0.6 units compared to bulk soils. A significant increase was also observed for DOC concentrations regardless of the soil type or total metal concentrations, which might be attributed to the plant root activity. For all studied soils, the rhizosphere SPW metal concentrations decreased significantly after plant growth compared to bulk soils which might be attributed to the increase in pH and effects of root exudates. Zn, Pb and Cd accumulated in plant organs and the higher metal concentrations were found in plant roots compared to plant shoots.

Conclusions

The restricted transfer of the studied metals to the plant shoots confirms the potential role of this species in the immobilization of these metals. Thus, P. euramericana Dorskamp can be used for phytostabilization of technosols.

     

Copper,Zinc, and Lead Fractions in Soils Long-Term Irrigated with Municipal Wastewater

Long-term irrigation with municipal wastewater may lead, even in spite of intense farming, to an accumulation of organic matter, nutrient elements, and trace metals in soils. Excessive increases of heavy metals may pose a potential risk to the food chain and provoke restrictions for the further cultivation of sensitive crops. Copper (Cu), zinc (Zn), and lead (Pb) forms in soils under long-term irrigation (for 100–120 years) with treated wastewater of Wroclaw were investigated by using selective seven-step sequential extraction (procedure of Zeien-Bruemmer) for partitioning the metals into operationally defined fractions, likely to be released in solution under various environmental conditions. The largest fraction of Cu, Pb, and particularly Zn in nonirrigated (control) soils was strongly bound in a residual form, while the percentage of exchangeable and the most labile fractions were negligible. Total concentration of metals in irrigated soils was elevated, and significant redistribution of metals among phases was observed. Percentages of residual fraction of Cu and Pb were no more than 25% (Zn < 40%), while significantly increased contribution of fractions occluded on iron (Fe) oxides and organically bound Cu. Exchangeable and readily mobile forms of Zn are predominant zinc fractions in soils irrigated with wastewater.     

Leaching of metals from the A-horizon of a spruce forest soil

The study quantifies the amount of metals (Na, K, Mg, Ca, Al, Fe, Mn, Ni, Cr, V, Cu, Zn, Cd, Pb) leached from the A-horizon of a podzolic spruce forest soil in southern Sweden during 2.5 yr, and offers statistical evidence of environmental conditions of importance to metal release. Considerable losses of Pb, Cr, Ni and V may occur from the A-horizon of forest soils under conditions favoring leaching of organic matter, Fe, and Al, i.e. during periods of comparably high soil temperature and moisture. Metals with a larger fraction present in exchangeable form (Na, Mg, Ca, Zn, Cd) are more susceptible to minor pH changes. An accelerated deposition or internal production of acidic matter therefore will reduce the retention times of these elements particularly.     

Heavy metal, pH, and total solid content of maple sap and syrup produced in eastern Canada

Maple sap and syrups in eastern Canada were analyzed for pH, total solids, and the heavy metals Cu, Fe, Pb, and Zn. The levels of heavy metals found were within the range normally contained in food and water samples except for Pb. The concentration factor found in reducing sap to syrup did not reflect the same concentration change for the measured parameters. This indicates removal or conversion of heavy metals and organic acids with the sugar sands. There was no statistical difference among provinces with respect to the heavy metal, pH, and total solids content of sap. The only significant difference in syrup occurred with Cu and this appeared to be the result of the processing procedure. As the season progressed, the Cu, Pb, pH, and total solids content of the sap decreased while Zn increased and Fe showed little change. Syrups reflected a similar change. Statistical differences occurred in sap composition among sites within each province.     

Applying Chemometrics to Determine Dispersion of Mine Tailing-Affected Sediments from Submarine Tailing Disposal in Bøkfjorden,Northern Norway

Mine tailing management is one of the largest environmental issues related to mining operation. This study uses chemometrics to assess the dispersion of iron mine tailing-affected sediments in Bøkfjorden, Northern Norway. Metal concentrations (Al, As, Cd, Cr, Cu, Fe, Mn, Ni, Pb, Zn) and physico-chemical sediment characteristics (conductivity, organic matter, sulphate, chloride, grain size, CaCO₃, pH) were analysed in seven sediment cores collected in a transect out of the fjord along with two reference cores. Results of hierarchical cluster analysis and principal component analysis allowed to distinguish between mine tailing-affected and non-affected sediments. Non-affected sediments were especially characterised by high levels of organic matter whilst mine tailing-affected sediments varied significantly in sediment characteristics depending on location in the fjord. Crucial parameters to reveal mine tailing-affected sediments varied between the target metal Fe along with metals of Cd and Mn, albeit less significant. Variations in mine tailing-affected sediment characteristics could be attributed to other anthropogenic activities in the fjord. Despite potential disturbances, chemometrics made it possible to identify dispersion of mine tailing-affected sediments to cover the inner and middle parts of the fjord. The study demonstrates the advantage of applying chemometrics on complex fjord systems, which in this case was used to distinguish mine tailing-affected sediments from areas with elevated levels of metals not necessarily related to the mine.     

二百方子沼泽湿地沉积物重金属分布特征研究

选取霍林河下游二百方子沼泽湿地为研究对象 ,采用重力沉积芯采样钻钻孔采样与剖面切割采样相结合的方法 ,采集了 8个沉积柱芯及剖面 ,对沉积物重金属元素Cu、Zn、Cr、Ni、Co、Pb、Fe、Mn及pH、总有机碳 (TOC)、全氮 (TN)在剖面中的分布进行高分辨率研究。结果显示 ,剖面上部沉积物表层沉积序列内已明显富集了Fe、Mn、Zn等重金属 ,并与TOC含量呈显著相关。与此相反 ,大多数沉积柱芯下层的重金属含量相对较低并接近地球化学天然背景水平。研究表明 ,高分辨率取样易找出元素间相关性。越靠近河流 ,淹没频率越高 ,沼泽湿地表层沉积物中重金属元素含量越高。     

Determination of the Lability Characteristics of Lead,Cadmium and Zinc in a Polluted Mediterranean Brackish-Marine Interface System

Labile and non-labile fractions of zinc, lead and cadmium are studied throughout the mixing process of the waters of a small brackish, polluted lake (Koumoundouros lake) with the seawaters of the adjacent Elefsis Bay, employing Differential Pulse Anodic Stripping Voltammetry (DPASV) and Chelex-100 resins. The metal fractions were classified according to their relative lability as: very labile, moderately labile, slowly labile andinert. Their distribution is determined mainly by their affinity to complexation to organic and inorganic ligands and the changes of pH and salinity. Furthermore, the impact of salinity and pH on lability was also studied using laboratory simulation experiments. Interesting observations on the phenomena recorded include: (a) positive correlation between salinity and the very labilefraction of the metals, attributed to the formation of ion pairs and complexes of metals with chlorine ions; (b) increase of the presence of the less labile metal species by increasing pH; (c) relatively strong correlation of the dissolved organic carbon with the slowly labile and inert fractions of Pb and Zn, respectively.     

Temporal Variability of Metal Contamination in Urban Road-deposited Sediment in Manchester, UK: Implications for Urban Pollution Monitoring

An important component of monitoring pollution of urban road-deposited sediment (RDS) is an understanding of the temporal variability in its composition and physical characteristics. This study set out to determine what the monthly variability in metal concentrations, organic matter content, grain-size and grain-size fraction metal-loadings are in inner city sites in Manchester, northwest England. The results show that there is significant temporal variability in metal (Pb, Zn, Fe, Mn) concentration in RDS from inner city Manchester. There was no significant temporal variability in grain-size characteristics or organic matter content, indicting that these metal variations were the result of variation in sources and accumulation processes. Pb and Zn displayed local variability, suggesting local controls on variability, whereas Fe and Mn displayed consistent variability across all sites, suggesting a common, larger-scale control on variability. The finest grain-size fraction (<63 μm) contained the highest Pb, Cu and Zn concentrations, but for the case of Fe and Mn, the coarser fractions (>300 μm) commonly contained the highest concentrations, again suggesting differing controls. For all metals, due to the weight percent dominance of the coarser fractions, the dominant loading of metals is in the coarser fractions. This has implications on management strategies, via street sweeping and the subsequent waste disposal, and on the modelling of the input of RDS and associated metals into surface waterways. The recognition of significant temporal variability of metal concentrations in RDS, independent of grain-size changes, implies that the monitoring of urban road sediment pollution will require not just consideration of spatial variability, but the design of schemes that will capture temporal variability also.     

云南滇池沉积物中重金属的形态分布特征

Fractionation of heavy metals in sediments can help in understanding potential hazards of heavy metals. The present study analyzed total concentrations and fractions of selected heavy metals （Cd, Cr, Cu, Pb, and Zn） in surface sediments from Dianchi Lake, Yunnan Province, China, as well as factors that may affect distributions of the various heavy metal fractions. Total concentrations of the heavy metals decreased in the order Zn 〉 Cu 〉 Pb 〉 Cr 〉 Cd. These heavy metals, except Cr, were much higher than their background levels, indicating that Dianchi Lake was polluted by Cd, Zn, Pb, and Cu. Cadmium occurred mainly as the non-residual fraction （sum of the HOAc-soluble, reducible, and oxidizable fractions） （97.6%）, and Zn （55.7%） was also predominantly found in the non-residual fraction. In contrast, most of the Cr （88.5%）, Pb （81.8%）, and Cu （59.2%） occurred in the residual fraction. Correlation analysis showed that total heavy metal concentrations, organic matter and reducible Fe were the main factors affecting the distributions of the various heavy metal fractions. In the Walhai section of Dianchi Lake （comprising 97% of the lake area）, the concentrations of Cd, Zn, Pb, and Cu in the non-residual fraction were significantly lower （P ≤ 0.01 or 0.05） than those of the Caohal section （3% of the lake area）. This indicated that potential heavy metal hazards in the Caohai section were greater than the Waihai section.