长江南京段近岸沉积物中重金属富集特征与形态分析

在对长江南京段八卦洲和杨中两个冲积洲近岸沉积物及其优势野生植物中A1、Cu、zn、Cr、Pb、Nj和Cd元素含量分析的基础上,分别考查了这些重金属的富集系数(EF)和生物富集因子(BCF),并采用BCR连续提取法对Cd的赋存形态进行了研究.结果表明,本区域长江近岸沉积物和野生植物中重金属存在不同程度的富集现象,两洲沉积物中Cu、Cr、Pb、Ni、Cd均有富集趋势,各元素EF>1的样品占总样品比例分别为Cu 50%、Cr40%、Pb40%、Ni 40%、Cd20%.而在野生桐蒿和芦蒿两种优势植物中Cd富集显著,其中桐蒿的BCF平均值高达2.57.采用BCR连续提取法对沉积物中Cd进行形态分析,结果显示,沉积物中Cd主要以酸溶/交换态(B1)和可还原态(B2)为主,二者分别为31.7%和45.5%,占到总量的70%以上,B1态远高于一般土壤和沉积物中重金属的分布,表现出很强的迁移性和生物可利用性.新生成沉积物较老沉积物中的B1态有显著增加,反映出沉积物越新,Cd的迁移性越强的趋势.研究结果说明长江城市段近岸沉积物中Cd受近期人为因素影响明显,具有一定的生态风险.     

AVS-SEM relationships and potential bioavailability of trace metals in sediments from the Southeastern Mediterranean sea,Egypt

In risk assessment of aquatic sediments, much attention is paid to the difference between acid volatile sulfide (AVS) and simultaneously extracted metals (SEM) as indicators of metal bioavailability. Distribution of AVS and SEM (Cd, Cu, Ni, Pb and Zn) were determined in 20 representative sampling sites collected along the Egyptian Mediterranean coast. Total SEM concentration [ΣSEM] ranged from 0.012 to 0.241 μmoleg^?1. AVS concentrations were much more variable, showing significant spatial variations. The values ranged from 0.015 to 31.326 μmoleg^?1. The different relationships between AVS and SEM to establish mechanical models such as the ratio of ΣSEM and AVS [ΣSEM/AVS], the difference between the ΣSEM and AVS [ΣSEM–AVS], or the organic carbon normalised difference between SEM and AVS [ΣSEM-AVS]/f_oc models were used as parameters to evaluate potential bioavailability. Considering SEM/AVS model, sediments at the Western Harbour, Eastern Harbour, Ras El-Burr, El-Gamil East, and Port Said stations are occasionally toxic, while according to SEM-AVS model, no indication of associated adverse toxic effect would occur at any of the sampling sites. Calculated [ΣSEM-AVS]/f_oc was<130 μmoleg^?1 in the sediments indicating that sediments should pose a low risk of adverse biological effects owing to cadmium, copper, lead, nickel and zinc. Association of adverse effects to aquatic organisms was determined, using the classification of the sediments according to the Sediment Quality Guidelines (SQGs). The marine Threshold Effect Levels (TEL) and Probable Effect Levels (PEL) were used in this work and in order to obtain a more realistic measure of predicted toxicity, mean PEL quotients (PELq) were calculated. The mean PELq calculated for the sampling sites was (0.11–1.5) and categorised as slightly toxic at all stations except Baghoush, Nobarreya and western harbour, which had PELq<0.1 and categorised as non-toxic. The obtained data concluded that the remobility and bioavailability of trace metals contained in surfacial sediments of the Egyptian Mediterranean coastal area are low.     

Heavy metals in surface water and stream sediments in Jamaica

The levels of heavy metals in water and stream sediments in Jamaica are presented and compared to levels in soils and environmental standards. Heavy metals (cadmium, chromium, copper, mercury, nickel, lead and zinc) appear to be less of a problem to Jamaica's freshwater environment than might be expected given the concentrations in soils. This can be explained by taking into account the dynamics of the Jamaican water environment and the relative absence of anthropogenic sources. The dynamics of the freshwater system on the other hand, could pass any environmental threat to the coastal environment. Because the stream sediments are relatively coarse and contain little organic material the bio-availability of micropollutants such as heavy metals from the sediments can be expected to be relatively high.     

Heavy metals in top core sediments from the southern Campania shelf (Italy): Hints to define large-scale geochemical backgrounds

The results of a geochemical survey carried out on the southern Campania shelf (southern Italy) are illustrated, offering a tempting opportunity to discuss the statement and definition of regional geochemical backgrounds for selected heavy metals. A total of 104 top core sediments, collected on average 1.5 km from one another and covering a shelf area of about 1300 km², were analysed for grain size, organic carbon content (OC), and heavy-metal (As, Al, Fe, Cd, V, Cr, Zn, Cu, Ni, Hg, and Pb) concentrations. The characteristics of the area, scarcely influenced by industrial activities, and the extensive data set, make this study suitable for an appropriate multivariate and spatial geostatistical methodologies used for i) a reliable definition of large-scale marine sediments' geochemical backgrounds and ii) an accurate discrimination of different geological controls on trace-element distribution patterns. Enrichment factors estimated with respect to both the average shale composition and the weighted average metal concentrations measured in inland soils rule out significant anthropogenic inputs. A spatial-geostatistics approach (kriging of spatial component based on an accurate implementation of variographic surveying) was applied, and this is proposed as an appropriate quantitative methodology to define the geochemical backgrounds for the different heavy metals. Two nested spatial structures were identified for some of the heavy metals, thus allowing clear identification of local and regional geochemical controls related to the different spatial variability of grain size.     

Extraction of anthropogenic heavy metals from reduced sediments: Indeterminations due to authigenic sulphides and clay minerals

A mineralogical and micro‐chemical study was performed by X‐ray diffraction and SEM/EDS techniques in a reduced sediment sample from the Venice Lagoon to investigate selectivity and significance of two widely used acid extractions (cold IN HCl and hot 8N HNO₃) for the evaluation of anthropogenic metal concentrations. Hydrochloric acid determines an incomplete and variable solubilization of authigenic iron sulphides, yielding a partial extraction of the associated metals (Hg, Mn, Zn and less Ni and Cu). Nitric acid is effective in solubilizing all sulphides, however, it leads to an overestimate of the anthropogenic metal content since it partially dissolves the lattice of some clay‐minerals, particularly chlorites. When these acid extractions are used to asses metal pollution in aquatic ecosystems, the possible over or under‐estimate of the anthropogenic concentration must be taken into account, considering the mineralogical composition of the sediment.     

Trace metal pollution in aquatic sediments and some fish species from the Kwilu-Ngongo River,Democratic Republic of Congo (Bas-Congo)

In this study, the concentrations of some metals in sediments and consumable fish from the Kwilu Ngongo River, province of Bas-Congo, Democratic Republic of Congo, are investigated. The digested muscle tissue, whole fish, and river sediment samples were subjected to trace element analysis by inductively coupled plasma mass spectroscopy and by using an automatic mercury analyzer. The highest values of trace metals in fish muscle tissue were found for Cr, Cu, Pb and Hg, with maximum values of 8.6 (Cr), 15.7 (Cu), 6.0 (Pb) and 3.3 (Hg) mg kg^?1. These values are higher than maximum tolerable limits recommended by the European Commission Regulation for Food. The highest metal concentrations in sediments were 81 (Cr), 86 (Cu), 21 (Sb), 41 (Pb), and 0.8 (Hg) mg kg^?1. Sediment toxicity tests using benthic crustaceans (ostracods) revealed mortality rates of up to 30% after six days of exposure to the sediments near the sugarcane industry outlet pipe discharge. The contamination of the sediments and fishes by the elements and the bio-accumulation of mercury in fish most likely arise from the adjacent agricultural fields where intensive sugarcane cultivation since 1925 has probably contaminated the soils through the long-term use of fertilizers and pesticides.     

Speciation of heavy metals in Albanian coastal sediments

This article presents results on heavy metal (Fe, Mn, Cr, Ni, Cu, Cd, Pb and Zn) speciation in the coastal sediments of Albania. Sediment samples were collected within the framework of the activities of the Interreg Italia–Albania Project, carried out in the Southern Adriatic Sea in 2000–01. This study shows that Albanian coastal sediments are highly influenced by river input, as the decreasing concentrations from coast to offshore confirm. Pb represents an exception of the general trend; meteoric inputs are prevalent for this metal. Ni, Cr, Fe, Zn and Cu correlate significantly and positively in the entire area, indicating a common origin for these metals in the analyzed sediments. All metals result mostly associated to the most refractory phases, which constitute up to 80% of the total concentration. Nevertheless a recent input of Cr, Ni, Cu and Mn can be observed, as the result of mining and industrial activities, in some selected areas, such as the Drin Bay and Durres. Their high concentration in the bioavailable phase can determine toxic effect upon biota.     

Heavy metals availability (Fe, Mn, Zn, Cu and Cr) in Aden Gulf sediments under aerobic and anaerobic conditions

The present study aims to analyse the chemical speciation of heavy metals in relation to aerobic and anaerobic conditions. Two sediment samples (from the Gulf of Aden, Yemen) were incubated under flooded conditions. In particular, the chemical forms of Fe, Mn, Zn, Cu and Cr under the experimental conditions were studied using a sequential chemical extraction method. The pH and Eh of the suspension were measured as critical parameters controlling the fate of the metals in the environment. The results showed that the metals concentration in the different forms varied with time incubation and affected by the variation of redox potential and pH value. Also, the changes in both redox potential (Eh) and pH values had evident effects on heavy metals transformation. It is obvious that the highest redox potential affected the amount of iron and manganese in the oxides form. When the redox potential decreased to-133 and-170 mV, it caused a significant transformation of the Fe-Mn oxide form to the water-soluble and exchangeable fractions. Under anaerobic conditions, the relative percentage of all five metals including the summation of four fractions (the water-soluble and exchangeable, carbonate, oxides and organic fractions) constituted 45-60% of the total amount of iron, 33-50% for manganese, 33-63% for Zn, 63-74% for Cu and 19-43% for Cr. Both zinc and copper among water-soluble and exchangeable fraction were high at the end of incubation period, this accompanied by a significant decrease in the content of the organically bound fraction. In general, the reducing conditions were more favorable for metal bound to water soluble and exchangeable fraction.     

The distribution of heavy metals in deposited urban dusts and sediments, Coventry, England

Samples of urban dusts and sediments have been collected and categorised into three compartment those which act mainly as sources, those undergoing transport and those which have been deposited. The sediments were fractionated into <63m to match similar sized lacustrine sediments and <2mm to represent natural and anthropogenic fluvially transported sediments. Preliminary results of total heavy metals analysis show that the <2mm fraction of the source group exhibits the greatest variabilty in metal concentrations. Overall, however, the <63m fraction dominates regardless of compartment. Some heavy metal concentrations decrease through the sourcetransportdeposit process, possibly due to selective onward transport of finer material or other anthropogenic processes unique to the urban environment (e.g. street cleansing). Sitespecificity is indicated in a comparison with other similar studies.     

羟基磷灰石对沉积物中重金属释放特性的影响

以羟基磷灰石掺杂前后模拟重金属污染沉积物为研究对象,利用混匀释放实验及化学连续萃取法分析沉积物中重金属的释放特征及形态分布特性,考察了羟基磷灰石对重会属污染沉积物中Cu、zn、Pb、Cd稳定性的影响.结果表明不同来源模拟污染沉积物中松花江沉积物中的重金属最易重新释放,而伊通河沉积物中的重金属释放量最小;同时伊通河沉积物中残渣态重金属的比例较其它沉积物高很多,而可交换态和碳酸盐结合态的重金属比例较其它沉积物低很多,说明同时进入沉积物中的重金属,伊通河沉积物中的重金属相对稳定一些.羟基磷灰石的掺杂不同程度降低了沉积物中重金属的释放能力,促使沉积物中的重金属由较不稳定结合态向较稳定结合态转化,减小了沉积物中重金属的生物可利用性,增强了重金属的稳定性.     

Levels of selected heavy metals in commercial fish from five freshwater lakes,Pakistan

The levels of As, Cd, Cr, Cu, Fe, Mn, Ni, Pb, Zn and Hg are estimated by atomic absorption in the muscle of six commercial species of fish belonging to five freshwater lakes of Pakistan. The species included Mastacembelus armatus, Tor putitura, Mystus seenghala, Wallago attu, Catla catla and Labeo rohita. The fish were procured in comparable weight ranges so that a viable comparison of trace metal content could be effected. As, Fe, Pb, Zn and Hg showed elevated levels of 0.006–6.967, 0.933–6.133, 0.060–4.108, 0.978–5.363 and 0.030–3.211 μg/g, wet weight. The relevant statistical parameters, such as standard deviation, standard error, skewness and its t‐value are also reported for establishing the randomness of the distribution in relation to the corresponding data of freshwater lakes of the world and examined in view of species‐specificity and origin.     

Geochemical forms of trace metals in mangrove sediments—Red Sea (Egypt)

Seven sediment samples from mangrove sediments of the Red Sea were taken in order to evaluate the possible contamination of the sediments by trace metals (iron (Fe), manganese (Mn), zinc (Zn), copper (Cu), lead (Pb) and cadmium (Cd)). Sequential extraction techniques were performed to study the different geochemical forms of these metals. X-ray diffraction analysis has been performed to correlate the mineralogical composition with the geochemical forms of the studied elements. The results of Fe and Mn contents indicate that they are in large part from lithogenous origin. The elevated concentrations are associated with the residual form ranged from 70 to 93% for Fe and 46 to 70% for Mn. The percentage of Zn, Cu, Cd and Pb in the non-residual form was much greater than that of the residual fractions. This reflects the high mobility and bioavailability of these metals in mangrove sediments of the Red Sea. X-ray diffraction analysis revealed the presence of silicate components including quartz, feldspars and clay minerals in some locality. Non-silicate components recorded in the study area as calcite as well as, Mg-calcite. Quantitatively both components i.e. silicate and carbonate varied according to their source material.     

Inorganic and organic contaminants in sediments from an urban playa and associated toxicity among Hyalella azteca

Playa wetlands are important components of the Southern High Plains (USA) landscape as they are the major aquatic surface feature. Chemical contaminants associated with playas have been documented, particularly for grassland and agricultural watersheds, but not for playas in urban settings. The objectives of this study were to determine concentrations of inorganic and organic contaminants in sediments from an urban playa within the I-20 Wildlife Preserve and Jenna Welch Nature Study Center in Midland, TX, and evaluate toxicity of these sediments to Hyalella azteca. Concentrations of most trace elements were below sediment quality guidelines with exceptions of lead, cadmium, and arsenic. Concentrations of organic contaminants, particularly PAHs, DDT, DDE, and malathion, were above sediment quality guidelines at various locations within the playa. Decreased survival was observed among H. azteca exposed to sediment from a single location when compared those exposed to reference sediments. This location also produced maximum observed concentrations for five of seven trace elements, potentially due to its location at the lowest elevation within the playa. This study documented concentrations of contaminants in sediments of an urban playa associated with past and present land uses in its urban setting, including those from automotive emissions and historical pesticide use.     

Chemical fractionation of metals in core sediments of Orogodo River,southern Nigeria

Sequential chemical extraction of metals (Cu, Ni, Mn, Fe, Pb, Cr, and Zn) from core sediments of the Orogodo River was carried out with a view of providing information on the phase distribution of these metals with respect to depths and seasons. The results indicate that copper was speciated into organic matter/sulfide, Fe–Mn oxides, and residual forms at 0–5?cm depth while at deeper sections copper was predominantly in the residual form. Nickel was speciated mainly into Fe–Mn oxides and residual forms. The average of lead in various particulate phases of the sediment are 0–100% for residual; 0–8% for carbonate; 0–16.2% for exchangeable; 0–10% for organic matter/sulfide form and 22–56% for Fe–Mn oxides bound metals. Manganese was speciated into exchangeable (10–36%) and Fe–Mn oxides bound (10–48%) at the surface layers of 0–20?cm depths and predominantly in the residual form in deeper sections implying partitioning into trioctahydral clay and/or well-defined crystalline oxides. Iron was predominantly in the Fe–Mn oxides and residual fractions, less than 8% in the organic fraction, and 24.4–37.3% in the exchangeable and carbonates fractions at the surface. The percentage contributions of iron in the exchangeable and carbonate fractions decreased to 3.2% at 55–60?cm depth. The amount of chromium in the exchangeable fraction ranged from 0% to 7% for exchangeable; 0–26.5% for organic matter/sulfide bound; 3.8–17.9% for Fe–Mn oxides; and 46.8–100% for residual fraction. The mobility factors of the metals indicated that these metals were relatively mobile at top sections as compared with deeper sections. The overall picture of metal mobility and availability indicates potential contamination risk by Fe, Zn, Mn, and Pb in the Orogodo River sediment system.     

Heavy metals contamination in mudflat and mangrove sediments (Mumbai,India)

The focus of this study, carried out on mudflat and mangrove sediments of Ulhas Estuary and Thane Creek in Mumbai, India, documents how sediment analysis in different ecosystems can help in understanding metal behaviour and pollution status of the region. Based on the the geoaccumulation index (I _geo ), the study shows that the estuarine and creek regions, being recipients of industrial and domestic wastes, display moderate pollution. Ulhas Estuary with higher clay and organic matter contents, exhibits higher amounts of metals than Thane Creek. Furthermore, using correlation and cluster analyses, the creek projects stable subenvironments with similar types of metal associations, with Fe and total organic carbon as the dominant metal carriers. By contrast, in the estuarine subenvironments, the metal associations do not reveal any distinct trend, which may be attributed to the disturbance caused by dredging activities routinely carried out in the region. Factor analysis carried out on I _geo data in both regions further helped in identifying polluted metal groups.     

成都市河流表层沉积物重金属污染及潜在生态风险评价

根据流经成都市内的三条河流（府河、南河、沙河）表层沉积物重金属数据，采用Hakanson潜在生态危害指数法对重金属的潜在生态风险进行了评价。结果表明（1）重金属潜在的生态危害因子（Er^i）说明大多属于轻微生态危害范畴，产牛生态危害的主要重金属是Hg、Cd，Cu、Pb次之，As影响最小；（2）多种重金属的生态系统的潜在生态风险指数（RI）表明河流重金属污染属于轻微生态危害和接近中等生态危害，其受危害程度由强至弱的次序为：府河，南河，沙河。     

Sediments distribution of trace metals in a coastal lagoon (Southern Sardinia,Mediterranean Sea): assessment of contamination and ecological risk

Coastal lagoons are subject to several sources of contaminations. To shade light on the contamination level of the Santa Gilla lagoon (Tyrrhenian Sea) we investigated the spatial distribution of Cr, Ni, Pb, Zn and Hg in sediments and their correlation with grain size and organic matter contents. Moreover, sediment contamination levels and the ecological risk associated with metal concentration were assessed using different abiotic indicators. The lagoon is characterised by low levels of contamination, with exceptions for Pb and Hg, whose distribution reflects the position of an old chlor-alkali plant and that of an airport. These results indicate that the restoration put in place 30 years ago have not reached the expected target and that the presence of the airport deserves further attention. In the outer section of the lagoon, where clam fishery occurs, we observed low levels of contamination suggesting that such artisanal fishery could somehow help mobilising metals. We conclude that the area exposed to Hg pollution, though tentatively restored, still suffers of a potential risk of ecosystem deterioration. We pinpoint that further investigations on the mobility, bioavailability and toxicity of metals are needed to finally address the actual impairment of the Santa Gilla lagoon.     

Temporal variation and distribution of trace metals in freshwater and fish from Calabar River, S.E. Nigeria

An investigation on the abundance and distribution of trace metals (Fe, Cu, Zn, Mn, Cr, Cd and Pb) in water, and nine species of fish samples from Calabar river was carried out in 1992. The concentrations of iron (6000–7240gl^–1), zinc (4910–7230gl^–1), and cadmium (3–7gl^–1) showed moderate pollution while those of copper (420–630gl^–1), manganese (23–48gl^–1), chromium (<10–20gl^–1) and lead (<1–10gl^–1) in water were well below WHO permissible levels. Significant seasonal changes (0.001p0.25) were obtained for iron, copper, zinc, manganese and cadmium in water. Furthermore, iron, zinc and cadmium showed statistically significant spatial changes (0.005p0.10). Of the nine fish species studied, no statistically significant relationship between body weight and the concentrations of the metals was observed. The concentrations of the metals per mean total body weight apparently decreases in the order Fe>Zn>Cu>Mn>Pb>Cd=Cr and were within the limits that were safe for consumption.     

镇江市古运河河岸沉积物重金属分布特征及潜在生态风险评价

对镇江市古运河河岸7个表层沉积物中重金属As、Cu、Pb、Cd、Zn、Cr含量进行测定,并通过富集系数、地累积指数法、潜在生态风险评价以及主成分分析等对沉积物重金属的分布特征进行综合分析与评价.结果表明:(1)古运河河岸带沉积物Cr、Cu、Zn、As、Pb和Cd元素的含量平均值分别为45.07、41.70、254.06、19.67、45.88、0.75 mg·kg-1,p H平均值为7.98.对比《国家土壤环境质量标准》可知,沉积物中Cu、Zn、Pb、As属于超一级标准,而Cd属于超二级标准.(2)6种重金属的富集系数表现为:AsCdPbZnCuCr,且综合富集系数在空间上表现为:G2G5G1G4G3G7G6;(3)古运河河岸表层沉积物地累积指数表现为AsCdPbCuZnCr,6种重金属中As富集量最大,Cr的富集量最小.(4)单项潜在生态危害系数结果表明,Cr、Cu、Zn、Pb均为轻微生态危害程度,As和Cd处于中等生态危害程度.从RI值判断,古运河河岸沉积物总体处于轻微生态危害.(5)相关性和主成分分析结果表明,Pb、Cu、Cr、Cd是决定第一主成分的4个主要因子,且Cu与Pb、Cd以及Pb与Cd元素具有相同的污染源.As、Zn在第二主成分中具有较高的载荷值,且As与Zn之间的相关性较弱,表明这两种重金属并非来自同一污染源.     

龙塘镇电子垃圾拆解区土壤和河流底泥重金属赋存形态及生态风险

龙塘镇是珠三角电子垃圾拆解区之一,采用AAS方法对该地土壤和河流底泥沉积物中5种重金属(Cd、Cr、Cu、Zn和Pb)含量进行测定分析,结果显示周围农田土壤中Cd含量是《国家土壤质量标准》二级标准的3倍左右,是广东省土壤背景值的20倍左右;拆解区土壤Cd超标最为严重,最高达5.67倍,超过广东省土壤背景值达36.17倍;拆解区下游0—1500 m河流底泥中Cd、Cr、Cu、Zn和Pb含量大幅增加且部分金属超标,Cd在0—40 cm深度内含量总体逐渐降低,仍远超背景值,Cu含量采样深度内递减规律最显著且在0—10 cm内含量超标,Cr、Zn和Pb除部分点位在表层积累较多外,其余与背景值相差不大且未超标.采用BCR(the Community Bureau of Reference)法提取重金属不同形态可知,底泥中Cd主要以弱酸溶态和可还原态为主,Cu主要以可氧化态存在,Cr主要以残渣态存在,而Zn和Pb则以可还原态为主;其中Cd的可提取态比例较高(60%),容易释放出来形成"二次污染".潜在生态风险结果表明,河流底泥中Cd生态危害程度属于极强(Ei320);其他金属Cr、Cu、Zn和Pb危害风险程度属于轻微(Ei40);金属Cd对整个RI值贡献最大(88%),应重点加强对Cd污染的防控.