Accumulation and Transport of Sediment Metals by the Vertically Migrating Opossum Shrimp,Mysis relicta

This study examined the accumulation of metals (Al, As, Cd, Cu, Cr, Fe, Ni, V, and Zn) in the opossum shrimp Mysis relicta from sediments to understand the contribution of sediment metals to overall body burden metal contents. Metal biota-sediment accumulation factors, tissue depuration ratios, and sediment metal assimilation efficiencies were calculated to examine the extent to which mysids accumulate metals from sediments contained within their guts. Results were then used to estimate the concentrations of metals transported to the water column and to fish because of mysid diel vertical migration. Results showed that Al, Cr, Fe, and V were readily depurated (34 to 73% of total body burden) and were not preferentially accumulated in mysid tissues (Biota Sediment Accumulation Factor, BSAF < 0.009). In comparison, As, Cd, Cu, and Zn were not readily depurated (9 to 26% of total body burden) and were more readily accumulated in mysid tissues (BSAF > 0.037). Nickel shows an intermediate behavior for depuration and accumulation. Calculations suggest that following 12 hours depuration through vertical migration, about 1.57 μg sediment/mysid (0.05% of dry weight of M. relicta) remained as gut contents. As a result, 16 to 50% of the Al, Cr, Fe, Ni, and V and 1.0 to 5.5% of the As, Cd, Cu, and Zn mysid body burden metal content transported to the water column was attributed to sediment in the gut. These results indicate that trace metals (As, Cd, Cu, and Zn) ingested from sediments are poorly accumulated in mysids (calculated AEs ranged from 0.07 for Cr to -11 for Cu) and metals transported by mysids to fish in the water column are primarily associated with mysid tissues.     

Biogeochemical Investigation of Big Creek Marsh,Lake Erie,Ontario

Geochemical composition of sediment, uptake of nutrients and metals by macrophytes, and nutrient and metal concentration in the water was investigated at six selected stations in Big Creek Marsh, Ontario. The maximum concentrations of Pb, Ni, Cu, Cr, and Zn in marsh sediment (86, 48, 38,119, and 383 μg/g dry weight, respectively), were lower than the concentration of these metals found in fine-grained surficial sediments of Lake Erie, and maximum concentration of As and Hg in marsh sediment (112 and 0.930 μg/g dry weight, respectively) were higher than As and Hg concentration in most of Lake Erie surficial sediments. Occurrence of DDT metabolites in marsh sediment reflects extensive use of DDT in the Big Creek drainage basin prior to 1970. Increase of total Kjeldahl Nitrogen and NH₄-N in marshwater was observed at a few sampling stations in November. Submerged macrophytes Myriophyllum, Chara, and Elodea sps. accumulated larger quantities of Pb, Cu, Ni, Cd, and Cr than emergent macrophytes at the stage of maximum development. Correlation between Ca and Pb, Cu, Ni, and Cr concentration in sampled macrophytes was observed; however, there was no correlation between Ca and Zn in these plants.     

Variations in trace elements in bottom sediments of major rivers in Lake Victoria's basin, Kenya

River sediments collected between March 1994 and January 1995 were analysed for iron (Fe), manganese (Mn), zinc (Zn), lead (Pb), copper (Cu), chromium (Cr), aluminium (Al) and cadmium (Cd) in the less than 63 μm grain‐size fraction. The river sediments were characterized by a sandy texture, with a relatively low organic matter (as percentage loss on ignition), ranging 3.5–9.6%. The metal mean range values in μg/g dry weight for the river sediments were: Mn (836–2.10 × 10⁴), Fe (1.09 × 10⁴–9.22 × 10⁴), Al (2.86 × 10³–7.77 × 10³), Zn (34–130), Cu (11–78), Cr (not detected ND–125); Pb (ND–100) and Cd (ND). Temporal variations were significant for Zn, Cr and Pb. There were no significant longitudinal differences in all the elements in rivers Nyando, Nzoia, Yala and Sondu‐Miriu, apart from sediment Fe contents. Relatively high sediment Fe, Mn, Zn, Cr and Al were observed in river Kasat. River Kasat was considered polluted with respect to Mn, Zn and Cr, which were comparatively higher than unpolluted sediments and geochemical background values. This supports similar results on surface water trace element levels. Most of the rivers drain an area of relatively similar lithological characteristics. Therefore, apart from the direct waste input into Kasat river from municipal and industrial sources, lack of specific point sources indicate lithological metal origins with localized variations. A final comparative evaluation of the river sediments’ trace metal pollution was made from the study results. The data is vital for pollution management of the lake as information about metal loadings into the lake ecosystem is lacking.     

Metals and Essential Elements in Herring Gulls from the Great Lakes, 1983

Adult and prefledged herring gulls were collected from one location each in Lakes Ontario, Erie, Huron, and Superior. Composite samples of liver, kidney, and feather were analyzed for 24 elements and composite samples of bone for 22 elements. After consideration of quality assurance results, concentrations of 16 elements (Al, Ca, Cd, Cr, Cu, Fe, Hg, K, Mg, Mn, Na, P, Pb, Sr, Ti, Zn) in liver, kidney, and feather were accepted for presentation while 6 elements were accepted from bone (Ca, Cd, Hg, P, Pb, Zn). Only lead, cadmium, and mercury values were of toxicological interest. Data on other trace elements are presented as baseline values among locations for each tissue and age class. Concentrations of Cd, Pb, and Hg were higher in adults than in prefledged young. Metal levels varied among different tissues with Cd highest in kidney (2.16 μg/g; Hamilton Harbour, Lake Ontario), Pb highest in bone (30.0 μg/g; Double Island, Lake Huron), and Hg highest in feather (6.11 μg/g; Middle Island, Lake Erie). Lead levels in both age classes were generally higher in tissues from the two upper lakes colonies than in samples from the lower lakes. Cadmium and mercury levels did not vary greatly among locations. Levels found are below those associated with metal toxicoses in laboratory studies with other avian species.     

Accumulation of Contaminant Metals in the Amphipod Diporeia spp. in Western Lake Ontario

Sediment and amphipods (Diporeia spp.) were collected in areas in western Lake Ontario suspected of containing a range of sediment metal contents. The total metal contents (Al, As, Cd, Cr, Cu, Ni, Fe, V, and Zn) of depurated Diporeia tissues were measured and compared to the total metal contents of the surrounding sediment. The fractional bioavailability of As, Cu, Fe, and Zn was determined in those same sediments using a sequential chemical extraction (SCE) procedure and correlated with depurated Diporeia tissue metal contents. Results of these analyses were then used to assess the ability of Diporeia to accumulate sediment metal contamination. A comparison of metal biota-sediment accumulation factors (BSAFs) and sediment metal enrichment factors (EFs) for each metal yielded separate metal groups showing different behavior for tissue accumulation. Aluminum, Cr, Fe, Ni, and V were not enriched in the sediments and were not accumulated in Diporeia tissues, while As, Cd, Cu, and Zn were enriched in the sediments and accumulated in Diporeia tissues. SCE results showed that Cu (3.2 to 8.4 %) and Zn (13 to 19 %) contents in the easily extractable sediment fractions (MgCl₂ and Na-acetate) were significantly correlated with Cu (r = 0.86; P<0.01) and Zn (r = 0.69; P<0.05) contents in depurated Diporeia tissue. In addition, Cu and Zn in Diporeia tissues are also correlated to the total sediment metal content for each respective metal (Cu: r = 0.67, P < 0.05; Zn: r = 0.66, P < 0.05). The high BSAFs for Cu and Zn, in combination with the association of tissue metal contents with easily extracted sediment metal fractions, suggest that Diporeia may be a potential bioindicator for Cu and Zn contamination in sediments.     

浸提时间对城市污泥重金属浸出特性的影响

在研究含工业废水污泥中Zn、Cu、Pb、Cr、Mn、Ni含量的基础上,应用固体废物浸出毒性方法,以不同浸出时间对污泥中重金属的浸出特性进行了实验研究.结果表明:污泥中Mn和Zn含量较高,其次为Cu和Ni,而毒性较大的Pb和Cr含量较低.浸提时间对污泥中重金属的浸出具有重要影响,污泥中的Zn、Cu、Ni最大浸出浓度在8h时,而Fe和Mn随着浸提时间增加而增加;浸提时间对污泥中重金属浸出量的影响因该重金属的化学性质不同而存在较明显的差别,这可能与浸提过程中的吸附-解吸过程、络合-解离过程和溶解-沉淀/共沉淀等因素有关.     

Comparison of surface functional groups and metal uptake efficiency of rice husk harvested from different climatic zones

Rice husk (RH) is a very effective natural adsorbent for fast removal of heavy metal cations from water solutions. Application of RH for removal of some heavy metal ions, such as Ni, Zn, Mn, Co, Cu, Pb and Cd from water solutions has been studied and different maximum adsorption capacities and a variety of optimized conditions were reported in the literature. In this work, the efficiency of RH harvested from different climatic regions was studied. For this proposal, different RH samples were collected from three different climatic regions of Iran (nominated as RH1 to RH3); their removal efficiencies of heavy metal cations of Ni(2+), Cu(2+) and Cd(2+) were investigated and compared. The adsorption data at optimum conditions could be assessed well by both Langmuir and Freundlich models. Statistical analysis of the results of adsorption isotherms showed that different RH samples have different efficiencies in uptake of these heavy metal ions. The RH samples were characterized using Fourier transform infrared spectroscopy and Boehm titration, which indicated that amounts of functional groups differed between RHs that are grown in different climatic conditions.     

Trace metal levels in sediments deposited in urban stormwater management facilities.

Characteristics of solids recovered from stormwater best management practice (BMP) facilities, including stormwater ponds, constructed wetlands, an infiltration basin, a biofilter, a stormwater treatment clarifier, and three-chamber oil and grit separators were described with respect to their metal chemistry. The reported trace metal concentrations in BMP sediments were assessed against the Ontario Sediment Quality Guidelines. Between 80 to 100% of all samples were marginally-to-intermediately polluted by Cd, Cr, Cu, Fe, Pb, Mn, Ni and Zn. Severe pollution of sediments was noted for Cr (122 microg/g), Cu (151 and 196 microg/g), Mn (1,259 and 1,433 microg/g), and Zn (1,116 microg/g), at several facilities studied, and even higher levels of metals were reported in the literature for certain oil and grit separators. With respect to individual BMPs, the severe pollution was found in sediments from oil and grit separators (for Cd, Cr, Cu, Pb and Zn), the stormwater clarifier sludge (Cu, Mn and Zn), a biofilter (Cu and Mn), an industrial area stormwater pond (Cu only), and a commercial/residential pond (Cr only). Finally, the chemical pollution of pond sediment triggered toxicity testing at some of the facilities studied, and sediment toxicity was confirmed at several sites.     

Zinc, lead and cadmium speciation in Dnieper water-bodies

Data on the concentrations and movements of Zn, Pb and Cd in Dnieper reservoirs and the Dnieper‐Bug estuary are considered. There is a clear trend of increasing concentrations, often two‐ to fourfold, of these materials from the 1960s to the end of the 1980s. Large increases may be explained as the result of increased human impact on the water‐bodies and also because of reduced water discharge in the Dnieper River (discharge has been reduced by nearly 10 km³ in recent years). At present, the average concentrations of Zn, Pb and Cd in Dnieper water‐bodies are 35.0–50.0, 15.0–18.0 and 0.5–1.8 μg L^–1, respectively. Anodic stripping voltammetry, membrane filtration, ion‐exchange and gel permeation chromatography on neutral sephadexes were methods used for analysis. The influence of adsorption and complexation processes on the mobility of Zn, Pb and Cd, and the ratio of their forms were compared. Ratios of free metal ions to ions bound in complexes with natural organic ligands were studied. The binding of metals in complexes with dissolved organic matter (DOM), or their adsorption onto suspended particles, were major processes reducing the concentration of free ions in their most toxic form. The percentage of Zn, Pb, and Cd free ions in the total balance of dissolved forms was no more than 3.6–4.8, 0.2–0.6 and 7.2–9.5%, respectively. The molecular‐weight distribution of organic metal complexes and their chemical nature, as well as the potential for complexing of DOM were investigated. Most Zn, Pb and Cd was found as complex compounds with DOM of different chemical natures and molecular weights. Humic substances, particularly fulvic acids, played a major role in the migration of the metals. These ligands bind from 40 to 80% of metals in the composition of organic complexes. Metal complex compounds of relatively low molecular weight (< 5000 Da) predominated in organic complexes of Zn (38–50%), Pb (38–52%) and Cd (22–47%). The role of inorganic ligands in complexation in surface waters was less important.     

Assessment of heavy metals in sediments and aquatic organisms in West Lake (Ho Tay), Hanoi, Vietnam

West Lake (Ho Tay) is the largest freshlake in Hanoi, Vietnam. It has a surface area of ≈ 500 ha and a total volume of >10⁷ m³, and is 1–3.5 m in depth. West Lake has been classified as needing protection because of its valuable freshwater genetic resources. Noting that it has been extensively affected by pollution, the objective of the present study was to examine the extent of heavy metal contamination of the sediments and commercially important biota in the lake. Heavy metal concentrations in the sediment from most of 24 samples in West Lake exceeded the Ontario Ministry of Environment Screening Level for chromium (Cr), copper (Cu), manganese (Mn), lead (Pb) and zinc (Zn) concentrations. Aquatic organisms from the lake also were found to be contaminated by heavy metals. The average Zn concentrations in snails and mussels tissues ranged between 174 and 415 µg g⁻¹, and the Pb concentrations between 3.5 and 5.2 µg g⁻¹. The Cu concentration in shrimp (52 µg g⁻¹) and snail (189 µg g⁻¹), and the Pb concentration in all fish species and shrimp from the lake (2.0–5.2 µg g⁻¹) exceeded the Food Standard Australia‐New Zealand (FSANZ) health standards for human consumption. The Cd concentration in Cyprinus carpio also exceeded the FSANZ standard. The implications of these study findings for the effective management of the food and ecological resources of West Lake are discussed.     

Comparative spatial metal concentrations and partitioning in bottom sediments of two tropical freshwater lake basins,Kenya

Metal concentrations in the water, sediments and biota in alkaline, near neutral water tropical freshwater lake basins were determined and a comparative analysis made on the spatial and accumulated trace metal concentrations, and geochemical partitioning of iron (Fe), manganese (Mn), copper (Cu), chromium (Cr), zinc (Zn), nickel (Ni), cadmium (Cd) and lead (Pb) in bottom lake sediments. Variable accumulated levels were found in the analysed sediments and aquatic biological tissues. Metal partitioning data in the present study from the two areas exhibits similar trends in magnitude. The residual fractions retained relatively higher amounts of metals. Relatively higher contents of Pb, Cr and Cu were found in Lake Victoria sediments. Cd, Ni, Mn and Pb are of concern because a higher percentage of these metals were retained in the more bioavailable fractions in Lake Naivasha. Total levels of sediment mercury were comparable for the two lake basins. Metals were found in significant levels in the tissues of aquatic organisms, highlighting the potential risks to other levels within the aquatic food chain. Although the exposure risk was not evaluated, it is important to continue monitoring these elements in fish, as sediments were found to contain considerable quantities of the metals. Numerous sediment extraction techniques data applied for evaluating metal partitioning in sediments cannot be compared because of the use of different methods. Nevertheless, the information is still useful in differentiating and understanding pollution loads from natural versus anthropogenic sources and their associated risks.     

The sorption of lead, cadmium, copper and zinc ions from aqueous solutions on a raw diatomite from Algeria

The adsorption of Cu(2+), Zn(2+), Cd(2+) and Pb(2+) ions from aqueous solution by Algerian raw diatomite was studied. The influences of different sorption parameters such as contact pH solution, contact time and initial metal ions concentration were studied to optimize the reaction conditions. The metals ions adsorption was strictly pH dependent. The maximum adsorption capacities towards Cu(2+), Zn(2+), Cd(2+) and Pb(2+) were 0.319, 0.311, 0.18 and 0.096 mmol g(-1), respectively. The kinetic data were modelled using the pseudo-first-order and pseudo-second-order kinetic equations. Among the kinetic models studied, the pseudo-second-order equation was the best applicable model to describe the sorption process. Equilibrium isotherm data were analysed using the Langmuir and the Freundlich isotherms; the results showed that the adsorption equilibrium was well described by both model isotherms. The negative value of free energy change ΔG indicates feasible and spontaneous adsorption of four metal ions on raw diatomite. According to these results, the high exchange capacities of different metal ions at high and low concentration levels, and given the low cost of the investigated adsorbent in this work, Algerian diatomite was considered to be an excellent adsorbent.     

Metal removal via particulate material in a lowland river system

Twelve month surveys of acid-soluble and dissolved trace metal concentrations in the lower Waikato River (in 1998/9 and 2005/6) showed abnormally low particulate Fe, Mn, Cu, Pb and Zn concentrations and mass flux in autumn, when the suspended particulate material (SPM) had a relatively high diatom and organic carbon content, and low Fe and Al content. Dissolved Mn, Cu and Zn concentrations also decreased in autumn, while dissolved Fe and Pb concentrations were unaffected. While SPM settlement under the low river flow conditions present in autumn can explain the removal of particulate metals, it does not explain dissolved metal removal. SPM-metal interaction was therefore investigated using seasonal monitoring data, experimental adsorption studies, sequential extraction and geochemical modelling. Pb binding to SPM occurred predominantly via Fe-oxide surfaces, and could be reliably predicted using surface complexation adsorption modelling. Dissolved Mn concentrations were controlled by the solubility of Mn oxide, but enhanced removal during autumn could be attributed to uptake by diatoms. Zn and Cu were also adsorbed on Fe-oxide in the SPM, but removal from the water column in autumn appeared augmented by Zn adsorption onto Mn-oxide, and Cu adsorption onto the organic extracellular surfaces of the diatoms.     

Prediction of trace metal distribution coefficients (KD) for aerobic sediments

Distribution coefficients for suspended sediments may be estimated from water and sediment quality variables, using detailed conceptual chemical models or semi-empirical models. The predicted K_D values find application in trace metal fate modelling and risk assessment. The detailed chemical model SWAMP (Sediment Water Algorithm for Metal Partitioning) which expresses trace metal distribution coefficients as a function of environmental variables and sediment characteristics was used to describe field K_D values. Besides SWAMP, semi-empirical models were derived from field-K_D values. The field K_D-values for Cd, Cu, Ni, Pb and Zn were measured on samples taken monthly from four surface waters in The Netherlands. In this paper we discuss the differences between the two modeling approaches.     

Assessment of sediment quality and pore water ecotoxicity in Kebir Rhumel basin (NE-Algeria): a combined approach

The objectives of this study are to use different approaches to assess the current pollution status in the wadis of the Kebir Rhumel basin. First, sediment trace metal contents were measured by flame atomic absorption spectroscopy. Then, sediment quality was assessed on the basis of contamination assessment indexes such as: Geoaccumulation Index (Igeo), Contamination factor (C(f)), Contamination degree (C(d)), Sediment Pollution Index (SPI) and SEQ guidelines (Consensus Sediment Quality Guidelines). In addition, several toxicity tests (Daphnia magna mobility inhibition acute test-48 h, Aliivibrio fischeri luminescence inhibition acute test - 15/30 mn and Pseudokirchneriella subcapitata growth inhibition chronic test - 72 h) were conducted to assess sediment pore water ecotoxicity. Trace metal concentrations followed the order: Mn > Zn > Pb > Cr > Cu > Ni > Co > Cd. Indexes used indicate varying degrees of sediment quality. Igeo, C(f), C(d) and SPI reveal a polymetallic contamination dominated by two or more elements in which Cd, Cu and Pb are of greatest concern. SEQ guidelines showed that biological effects on fauna would likely be observed occasionally and/or frequently for Cd, Cr, Cu, Pb and Zn contents. Test organisms exposed to sediment pore water showed that the algal P. subcapitata test was more sensitive than the D. magna and A. fischeri tests. Hence, algal growth inhibition proved to be the most sensitive response to contaminants present in sediment extracts but a significant relationship with trace metal contents was not demonstrated.     

Prolonged deposition of heavy metals in infiltration facilities and its possible threat to groundwater contamination.

A field investigation of infiltration facilities, built two decades ago in Tokyo, was carried out and sediment samples were collected from 12 infiltration inlets of three different locations. Heavy metals contents in the inlet sediment, road dusts and soils samples were analysed and compared. The particle size distribution analysis showed its variation in depth as well as from inlet to inlet. The nature of organic substances present in sediment found changes in particle sizes as well as in depth. The heavy metals content in the sediment samples ranged from 6-143 (Cr), 1-84 (Ni), 49-331 (Cu), 210-2186 (Zn) and 2-332 (Pb) microg/g. The heavy metal content ranges were similar to road dust, which indicated road dust as a possible source for sediment for the infiltration inlets. The lower heavy metals content in many sediment samples than the soil indicated possible release/desorption of heavy metals under newly created environments such as an anaerobic environment. Among the heavy metals there was a relatively good relationship between Cu and Zn, indicating the existence of their common sources.     

Fractionation of heavy metals in sediment cores from the Ell-Ren River,Taiwan

Fractionation of heavy metals (Cr, Cu, Co, Zn, Ni, and Pb) in sediment cores taken from three heavily polluted locations of the Ell-Ren River in southern Taiwan was studied. After the three sediment cores were separated into several depth sections, sequential extraction procedure was used to determine the variations in heavy metal binding fractions (exchangeable, bound to carbonates, bound to Mn oxides, bound to Fe oxides, and bound to organic matter) with different sediment depth, and followed by multivariate analyses. It turns out that a deeper sediment depth tended to result in smaller amounts of total extractable heavy metals (TEHMs), indicating that heavy metal pollution of the river has been intensifying these years. The decreasing order of TEHMs was: Zn > Cu > Pb > Cr > Ni > Co. The TEHMs Zn and Cu detected from different depth of the three sediment cores were mainly originated from “bound to carbonates” and “bound to organic matter” fractions, respectively. Also, the percentages of the heavy metals contained in each of the five binding fractons only slightly varied with sediment depth. From multivariate analyses, all the heavy metals except Co behaved similarly and might be discharged from the same pollution sources.     

松花江流域鱼体内重金属含量的监测与污染评价

为研究松花江流域鱼体重金属的污染现状,采用微波消解-电感耦合等离子体质谱法测定松花江流域鱼类体内的Cu、Zn、Cr、Cd、Pb、Hg、As等7种重金属的残留量,使用综合污染指数法对污染情况进行了评价。结果表明,松花江鱼体中7种重金属的基准值由高到低依次为Zn、Cu、Cr、As、Pb、Hg和Cd,且除Hg以外,其他6种重金属的来源具有一定的相似性;第二松花江流域中鱼体内重金属残留量高于嫩江和松花江干流两条流域中鱼体内重金属残留量;参照《无公害食品水产品中有毒有害物质的限量标准》(NK 5073-2006)和《食品中锌限量卫生标准》(GB13106-1991),鱼体内Pb、As、Cr和Zn的超标率很高,特别是Pb和As的污染比较严重。     

Spatial and seasonal variations and ecotoxicological significance of sediment trace metal concentrations in Kebir-Rhumel basin (Northeast of Algeria)

This study sought to assess sediment contamination by trace metals (cadmium, chromium, cobalt, copper, manganese, nickel, lead and zinc), to localize contaminated sites and to identify environmental risk for aquatic organisms in Wadis of Kebir Rhumel basin in the Northeast of Algeria. Water and surficial sediments (0-5 cm) were sampled in winter, spring, summer and autumn from 37 sites along permanent Wadis of the Kebir Rhumel basin. Sediment trace metal contents were measured by Flame Atomic Absorption Spectroscopy. Trace metals median concentrations in sediments followed a decreasing order: Mn > Zn > Pb > Cr > Cu > Ni > Co > Cd. Extreme values (dry weights) of the trace metals are as follows: 0.6-3.4 microg/g for Cd, 10-216 microg/g for Cr, 9-446 microg/g for Cu, 3-20 microg/g for Co, 105-576 microg/g for Mn, 10-46 microg/g for Ni, 11-167 microg/g for Pb, and 38-641 microg/g for Zn. According to world natural concentrations, all sediments collected were considered as contaminated by one or more elements. Comparing measured concentrations with American guidelines (Threshold Effect Level: TEL and Probable Effect Level: PEL) showed that biological effects could be occasionally observed for cadmium, chromium, lead and nickel levels but frequently observed for copper and zinc levels. Sediment quality was shown to be excellent for cobalt and manganese but medium to bad for cadmium, chromium, copper, lead, nickel and zinc regardless of sites.     

南昌市湖泊重金属源识别及污染特征风险评价

为了解南昌市湖泊重金属污染特征现状,论文以青山湖、象湖及前湖为研究对象,在分析湖泊水体及沉积物重金属Cr、Ni、Cu、Zn、Cd、Pb水平的基础上,采用因子分析、地质累积指数与综合潜在生态风险指数对湖泊重金属污染水平进行评价,并结合主成分分析等统计方法判别各研究水域重金属污染源。结果表明水域中Cr、Cd与Pb为主要重金属污染元素,前湖面临着最为严重的水体重金属污染。沉积物中Ni、Cu、Zn、Cd、Pb存在不同程度风险,各湖泊中沉积重金属风险程度从大到小均为Cd>Cu>Pb>Ni>Zn。前湖生态风险程度最大,其次是象湖。主成分分析表明湖泊重金属主要来源于交通运输与废水废气排放。因此为避免进一步污染,应合理规划交通,控制汽车尾气排放,提升污水治理水平。