珠海近岸海域表层沉积物中的重金属及生态危害评价

为了研究珠江口近海海域重金属的污染状况,2009年8—12月对珠海珠江口4个站点的表层沉积物进行了6次采样,测定了表层沉积物中重金属Cd、Cr、Pb、Hg、Cu、Zn、Mn、Ni、Fe和金属Al的质量分数,分析了它们质量分数间的相关性,依据Lars Hakanson提出的沉积物中金属污染物评价方法,对Cd、Cr、Pb、Hg、Cu和Zn等6种典型重金属的潜在危害进行了评价。结果表明,Cd、Cu和Zn是该调查区域的主要重金属污染物,应该予以优先控制和治理。位于马骝洲水道入海口的S1位点上,金属元素（Cd除外）质量分数的季节特征是秋季（丰水期）〈冬季（枯水期）,重金属危害指数（RT）为轻微级,重金属潜在生态危害系数（Eir）顺序为Cd〉Hg〉Pb〉Cu〉Zn〉Cr;在S2位点,Cd、Cu、Hg、Ni和Fe的平均质量分数为秋季〉冬季,其它5种金属则为秋季〈冬季,RT为强级;在S3、S4位点上,8种金属元素（Hg、Mn除外）的质量分数呈现秋季〉冬季的现象,RT为很强级;S2、S3和S4站点的Eir均表现为Cd〉Hg〉Cu〉Pb〉Zn〉Cr的顺序。     

湛江湾红树林湿地表层沉积物重金属形态特征、生态风险评价及来源分析

随着工业化与城市化进程加快,湛江湾重金属污染物入海量逐年增加,沿岸红树林湿地承受着愈来愈大的环境压力。为了解湛江湾红树林表层(0-15 cm)沉积物重金属污染状况,对湾内沉积物中8种重金属元素(As、Cd、Cr、Cu、Hg、Ni、Pb、Zn)的质量分数、赋存形态特征及潜在生态风险进行了研究。采用改进BCR提取法分析重金属形态特征,运用基于总质量分数的潜在生态风险指数法和基于形态学的次生相与原生相分布比值法与风险评估编码法进行风险评价,并结合多元统计方法对重金属来源进行解析。结果表明,(1)沉积物中除Cr、Pb外,其余6种重金属的质量分数平均值均超过雷州半岛土壤环境背景值;8种重金属空间分布差异明显,变异系数在37.24%-108.19%之间。(2)As、Hg以残渣态为主要赋存形态,Cd、Zn以酸提取态为主要赋存形态,Cu、Ni、Pb以可还原态为主要赋存形态,Cr、Ni以可氧化态为主要赋存形态。(3)8种重金属元素非残渣态所占比例排序依次为CdCuNiZnPbCrAsHg,其中Cd、Cu、Ni、Zn、Pb、Cr的非残渣态所占比例均超过70%,说明重金属元素具有极强的迁移性和生物有效性,再次释放风险较大;非残渣态质量分数高值区出现在NHD和GHCL站位,说明这两个区域红树林沉积物重金属活性较高,重金属污染问题应引起重视。(4)湛江湾红树林表层沉积物中重金属RI均值为273.076,为中等潜在生态风险;而总体RSP值为5.79,表现为重度污染。从空间分布看,各站位重金属元素为中度至重度污染;其中NHD站位重金属污染程度最高,RSP值为11.97,与非残渣态空间分布特征一致。(5)多元统计结果表明,湾内红树林表层沉积物中重金属来源主要与生活排污、养殖排污和工业排污有关,其次为自然风化产物的输入。     

洞庭湖湘江入湖口至出湖口水域表层沉积物中重金属时空分布特征与生态风险

基于2007—2012年连续对洞庭湖湘江入湖口至出湖口水域5个采样点的表层沉积物中Cd、Hg、As、Cu、Pb、Cr和Zn等7种重金属含量分析,对该水域表层沉积物中重金属的时空分布特征进行了探讨,并采用沉积物质量基准法对其生态风险进行了评价.结果表明,Cd、Hg、As、Cu、Pb、Cr和Zn的含量分别为0.54—79.90 mg·kg-1、0.046—0.712 mg·kg-1、15.2—289.0 mg·kg-1、29.0—217.0 mg·kg-1、6.0—246.0 mg·kg-1、65.4—269.0 mg·kg-1和41.4—632.0 mg·kg-1,其大小顺序为ZnCrPbCuAsCdHg;Cd、Hg、As、Cu、Pb和Zn含量沿程总体呈"V"形变化趋势,Cr含量沿程变化较小,重金属含量年际变化较为稳定;As具有较高生态风险,其余污染物具有较低生态风险,不同污染物生态风险的大小顺序为AsCdCrCuPbZnHg,S1和S3具有较高生态风险,其余点位具有较低生态风险,不同点位生态风险的大小顺序为S1S3S5S2S4.     

黄河中下游干流沉积物中重金属的赋存形态及其生态风险

在黄河中下游干流采集6个表层沉积物样品,采用Han和Banin连续提取法提取并采用ICP-MS和ICP-OES测定不同化学形态的Pb、Cu、Cd、Cr、Ni、Zn、Mn含量,在计算重金属富集因子、迁移系数、次生相和原生相分布比值的基础上,对重金属赋存形态、迁移能力、生物活性、污染状况和潜在生态风险进行了研究.结果表明,黄河中下游干流表层沉积物中重金属元素含量沿河流向先增加后降低,高含量点位出现在汜水汇入黄河后,支流的输入对黄河重金属含量具有较为明显的贡献.形态分析研究表明,Pb、Cu、Cr、Zn、Ni等5种重金属残渣态在其不同形态中有绝对优势,Cd可浸取态占明显优势,Mn的残渣态与可浸取态所占比例相当.富集因子分析表明,黄河中下游表层沉积物中重金属可分为3类:Cu、Cr、Mn基本无富集,Pb、Ni、Zn轻度富集,Cd中度到极高度富集;迁移系数研究表明黄河中下游表层沉积物重金属迁移系数和生物活性顺序为MnCdZnNiPbCuCr.次生相原生相比值法表明Cu、Cr、Ni、Zn无污染,Pb在3点位轻度污染,其它点位无污染,Mn在1、3、6点位轻度污染,其它点位无污染.综合各种评价方法,Cd是黄河中下游沉积物中污染程度最高的重金属,具有潜在生态风险,应引起重视.     

鄱阳湖湖口段沉积物重金属污染特征及潜在生态风险评价

为了解鄱阳湖与长江交汇区沉积物中重金属含量以及各污染物的潜在生态危害程度,通过采样分析As、Cd、Cr、Cu、Hg、Pb、Zn等7种重金属含量及污染特征分布的基础上,采用地积累指数法和潜在生态风险指数法对鄱阳湖底泥中的重金属污染进行综合性的评价分析.结果表明,鄱阳湖湖口段沉积物已经受到了不同程度的重金属污染;沉积物中Cd、Cu和Hg受人为影响比较严重,Cr、Cu、Hg、Pb和Zn均存在一定程度的积累;区域重金属元素潜在生态风险主要受制于Hg和Cu,潜在生态风险贡献率大小排序为:Hg(38.4%)Cu(27.8%)Pb(10.9%)Cd(9.1%)As(8.0%)Cr(4.0%)Zn(1.8%).     

珠江磨刀门河口表层沉积物中重金属含量及其分布特征

分析了在珠江磨刀门河口采集的37个表层沉积物样品重金属(Cu、Pb、Zn、Cr、Cd、Hg、As、Ni)的含量及分布特征。采用原子吸收法分析了Cu、Pb、Zn、Cr、Cd、Ni的含量,采用冷原子吸收法分析了Hg、As含量。结果表明,口门处及其两侧和拦门沙内坡重金属的含量最高;外海区域重金属含量普遍较低;由口内河床至口门处,Cu、Cr、Hg、As的含量减小,Pb、Cd、Zn、Ni的含量逐渐增大;大部分重金属(Cu、Pb、Zn、Cd、As、Ni)的含量由口门处至拦门沙地区是先减小再增大的;由拦门沙至外海,Cu、Pb、Cd、As的含量减小,Zn和Ni的含量先减小后增大;由口门处至外海,Cr和Hg含量的总体趋势是增大的。磨刀门河口表层沉积物中重金属元素含量与CEC、小于0.001mm粘粒以及沉积物有机质含量的相关性均达到显著或极显著水平;重金属含量与沉积物pH值的相关性不显著;重金属元素的含量变化和分布规律还表明磨刀门表层沉积物的重金属主要受陆源污染物的影响。     

庄河青堆子湾海水和沉积物重金属分布特征

利用电感耦合等离子体质谱仪和测汞仪对庄河青堆子湾近岸海水和沉积物中重金属含量进行了测定,分析了其时空分布特征及其与其它环境要素之间的相关性,同时对重金属污染状况进行了评价.结果表明,海水和沉积物中的Zn元素含量相对偏高;海水中Cu、Zn、Cd、Pb、Cr的分布受到相同因素的影响;青堆子湾近岸海水和沉积物受重金属污染尚不明显.     

莱州湾表层沉积物中重金属时空分布、污染来源及风险评价

运用污染风险评价标准和方法研究了2010年5月(春)、8月(夏)、10月(秋)和12月(冬)莱州湾表层沉积物中7种重金属污染物的时空分布特征、来源及生态风险。结果表明,表层沉积物中Cr、Zn和Pb含量均呈现春季低于其他季节特征,秋季Hg含量是其他季节的4倍,Cu、As和Pb含量无显著季节差异。表层沉积物中Cr、Cu、Zn、As和Cd最高值出现在莱州湾中部及小清河河口等西部水域,来源呈现受自然作用影响较大的特征;而Hg和Pb最高值出现在龙口和界河河口等东部水域,来源呈现受周边工业污染物的人为排放影响较大的特征。基于地理累积指数、生态效应浓度以及Hakanson潜在生态风险指数的综合评价表明,13%~29%的研究区域的表层沉积物受到轻微程度的Cd、Hg和Pb污染,Cd和Hg高值水域达到中等生态风险程度;Hg和As在65%~68%的研究区域的表层沉积物中达到可能对沉积物底质环境及生物群落产生不利生态影响水平。基于对重金属污染物的评价结果,莱州湾表层沉积物质量较好,局部区域存在Hg、Pb、Cd和As的潜在污染风险。     

东平湖表层沉积物重金属的空间分布及污染评价

为了解东平湖沉积物中重金属的污染特征,于2013年11月环湖采集了44个表层沉积物样品,分析了Al、Cd、Cr、Cu、Fe、Ni、Pb、Zn、Hg、As、有机质的含量和粒度,采用克里格(Kriging)插值法探讨了重金属的空间分布特征,并采用富集因子法和潜在生态风险指数法对其进行了污染评价。结果表明:东平湖表层沉积物有机质的平均质量分数为22.4g·kg~(-1);平均粒径为25.5μm,以粘粒和粉粒为主;Cd、Cr、Cu、Ni、Pb、Zn、Hg和As的平均质量分数分别为0.299、78.7、43.8、37.3、22.4、100.0、0.030和17.3 mg·kg~(-1)。各重金属含量较高的区域主要位于大汶河入湖口即湖区的东部、东南部,其次位于南部湖区;Hg和As在湖区北部即出湖区部分区域含量也较高。以黄河干流沉积物化学元素的背景值为评价标准,Cd、Cu和Zn表现为中度污染,其他重金属元素为轻微污染;总体生态风险水平为中等,其中Cd和Hg是主要的生态危害因子,其对潜在生态风险指数的平均贡献率分别为46.5%和29.6%。大汶河入湖区和出湖区部分区域表层沉积物重金属具有强生态风险。Cd、Cr、Cu、Ni、Pb和Zn之间具有显著的正相关性,与受人类活动影响较小的Al和Fe亦呈显著正相关,结合其空间分布特征和污染水平,推断Cd、Cr、Cu、Ni、Pb和Zn的来源受到自然源和大汶河污染输入的双重影响;而Hg和As与其他重金属元素间的相关性不显著,其可能还来源于湖区的渔业养殖、化肥农药、垃圾和生活污水等面源污染,但具体成因仍有待进一步研究。     

浙江省海盐县河流水体表层沉积物重金属生态风险评价

以浙江省海盐县水体监测断面位置处表层沉积物为研究对象,分析了表层沉积物中As、Hg、Cu、Pb、Zn、Cr、Ni和Cd这8种重金属元素含量和形态分布,采用地累积评价法(Igeo)、潜在生态危险指数(IR)、沉积物质量基准(SQC)、平均效应区间中值商法(m ERM-Q)和形态分析等方法评价了重金属的生态风险。研究结果表明:海盐县沉积物中As、Cd、Cr、Cu、Ni、Pb和Zn均呈现不同程度的污染,以Zn污染最为普遍。地累积评价指数法评价结果显示,大部分水体沉积物重金属呈轻度到偏重度污染,其中Zn和Cd呈轻度以上污染的分别达16和10处。潜在生态危害指数评价结果显示,单个重金属的潜在生态风险指数(Er)由大到小的排列顺序为CdHgAsCuPbNiZnCr,Cd是研究区域内主要的生态风险元素; IR评价结果显示,采样点HN6、HN11和HN20的IR分别为263、193和269,生态风险等级达中等级别。SQC评估结果显示,不同采样点处沉积物中重金属污染水平不同,且对水生生物影响不同; m ERM-Q亦显示各采样点位沉积物中重金属均有不同程度的生态风险。研究区域沉积物中Cr主要以不可迁移态存在,而其他重金属则主要为可提取态,需要重视环境改变后沉积物中重金属的二次污染问题。     

珠江三角洲工业区土壤(沉积物)重金属污染特征及防治对策--以石龙和容桂工业区为例

对珠三角两个代表性乡镇工业区的土壤（沉积物）重金属污染现状和来源进行了评价。结果表明,两工业区在主要污染元素类型和综合污染程度上很相似,表层土壤（沉积物）均以Hg、As、Cu的污染为主,且均以Hg的污染最严重;但在某些次要污染元素种类以及某些主要、次要污染元素的单个元素污染程度上存在一些差异。柱样沉积物中重金属的变化特征进一步说明,两工业区土壤（沉积物）中重金属的累积与我国尤其是本地区的工农业发展阶段和发展水平密切相关。文章最后提出了乡镇工业区土壤（沉积物）重金属污染的几点建设性防治对策。     

Correlation between levels of some heavy metals in plants and sediments from a segment of Calabar River and associated creeks in Cross River state of Nigeria

Plants and sediments were collected at three sites along Calabar River (CR), Upper Town Creek (UCC) and Lower Town Creek (LCC). The CR is a major tributary of Cross River, Nigeria. The concentrations of 10 heavy metals were determined and results for Fe, Mn and Zn at almost all the sites showed that the levels of these metals exceeded the amounts present in non-polluted areas. Fe was found in the highest concentration at all three sites in both plants and sediments. Correlation analysis between levels of heavy metals in plants and sediments were also determined. The occurrence of higher concentrations of heavy metals in plants and coastal sediments at CR, UCC and LCC is an indication of anthropogenically induced pollution rather than contributions from natural sources.     

洞庭湖主要入湖口表层沉积物重金属分布特征与生态风险评价

尽管针对洞庭湖沉积物中重金属的研究工作较多,但缺乏针对其主要入湖口的研究。基于2014年12月和2015年6月对洞庭湖主要入湖口表层沉积物中重金属调查,分析了重金属含量的时空分布特征,并采用一致性沉积物质量基准法对其生态风险进行了评价。结果表明,Cd、Hg、As、Cu、Pb和Zn的平均含量分别为3.27、0.190、27.10、39.8、38.0和157.8 mg·kg-1,其大小顺序为ZnCuPbAsCdHg,Cd和As含量出现超过土壤环境质量三级标准的现象,是主要的重金属污染物。Cd、As、Pb和Zn等4种重金属含量的最高值均出现在湘江入湖口,Cu含量的最高值出现在资水入湖口,Hg含量以沅江入湖口最高,除Pb外,其他5种重金属在湘江和资水入湖口的含量均大于平均值,表明湘江和资水入湖口污染较为严重;汛期与非汛期6种重金属的含量均无显著性差异(P0.05)。6种重金属生态风险大小顺序为AsCdZnPbCuHg,各入湖口生态风险大小顺序为湘江入湖口资水入湖口沅江入湖口汨罗江入湖口澧水入湖口长江"三口"新墙河入湖口,其中湘江和资水入湖口为较高生态风险,其他入湖口为较低生态风险。入湖河流是洞庭湖湖体沉积物重金属污染的主要来源,在一定程度上,入湖河流沉积物中重金属的含量对洞庭湖湖体沉积物中重金属污染状况起着决定性作用,因此,洞庭湖流域重金属污染防控应以入湖河流为主,其中尤以湘江和资水为重点。     

湘江衡阳段沉积物中铊等重金属的污染特征及其生态风险评估

湘江是我国重金属污染最重的河流之一。为了更全面了解湘江衡阳段表层沉积物重金属污染现状及其潜在生态风险,在前期相关研究基础上,分析了重金属Tl及其他4种重金属(Mn、Co、Ni和V)的含量水平和分布特征,并采用地累积指数法和潜在生态风险指数法对沉积物中重金属污染现状和潜在生态风险进行了评价。结果表明,湘江衡阳段表层沉积物中Tl和Mn有一定程度的累积和污染,其含量分别为0.12～2.09mg·kg-1和234～4580mg·kg-1。由于Tl具有较强的毒性响应,其潜在生态风险不容忽视。综合前期相关研究结果,研究区域中10种重金属总潜在生态风险指数(RI)为27.8～6266,约70%采样点具有重度生态风险,其主要风险来源于Cd和Tl。     

Anthropogenic metal pollution in surface sediments of the Tambaraparni River Estuary

Estuarine sediments in the<63 μm size fraction were collected from 15 stations within the Tambaraparni River Estuary, located on the east coast of India. The distribution of the heavy metals Cd, Co, Cr, Cu, Ni, Pb and Zn was recorded. Our analysis distinguished two groups of elements. First, Cd, Pb and Zn, which occurred in higher than expected concentrations indicative of pollution, and second, Co, Cr, Cu and Ni, which occurred at background levels. The highest metal concentration found in the study area was for Zn (1200 μ g·g^?1), and the lowest was for Cd (0.42 μ g·g^?1). It is presumed that river run-off, industrial waters and untreated domestic waters are major contributors to heavy metal pollution in the Tambaraparni River Estuary. The concentrations of heavy metal species in surface sediments (<2 m water depth) of the Tambaraparni Estuary were studied to determine the extent of anthropogenic inputs from catchment areas and to understand anthropogenic effects on geochemical process in this tropical estuarine system.     

Heavy metals associated with reduced sulfur in sediments from different deposition environments in the Pearl River estuary, China

Distribution of acid volatile sulfur (AVS) and the simultaneously extracted metals (SEM: Cu, Pb, Zn, Cd, Ni) in sediment profiles has been studied at five sites in Pearl River estuary, China. Of the five sampling locations, Nos.1 and 2 are in the middle shoal, Nos.3 and 4 in the west shoal and No. 5 locates to the south of the estuary. The AVS content in the sediments of the middle shoal varies in a small range (0.25–4.06 μmol g⁻¹), while that of west shoal increases with depth from 0 to ultimately 26.09 μmol g⁻¹. The SEM concentration in the sediment profiles at location Nos. 1, 2 and 5 is generally in the range of 0.95±0.2 μmol g⁻¹ with a slight upward increase, while that in the sediment of west shallows are much higher (1.43–2.42 μmol g⁻¹) with a significant upward increase, especially in the upper layer of ca. 15 cm. The observed upward increase of SEM content at all the sites implies that heavy metal contamination of sediment in the Pearl River estuary is increasing. Calculations of the excess heavy metal content which is defined by SEM-AVS molar difference suggests that the upper sediment in the Pearl River estuary, especially on the west shallows, could be a source of heavy metal contaminants and may cause toxicity to the benthos. The site-specific distribution patterns in the AVS and SEM profiles were interpreted according to the hydrogeochemistry of deposition environments.     

城市湖泊表层沉积物中的重金属污染现状及其风险评价——以武汉墨水湖为例

水体沉积物中的重金属会对生态系统构成直接和间接的威胁.为了研究工业化、城市化过程中城市湖泊沉积物重金属污染现状及其暴露风险，以武汉市墨水湖为研究对象，测定了5种重金属Zn、Cu、Ni、Pb及Cr在表层沉积物中的含量，分析了其污染程度、分布特征，并对其稳定度进行了分析.结果表明，墨水湖表层沉积物重金属污染程度较重，在所有采样点5种重金属含量均高于最低效应阈值（LEL），多数采样点甚至超过了严重效应阈值（SEL）.该湖泊沉积物中重金属分布具有比较明显的空间差异性：排污口区>湖中心水域>城区岸边带>林田岸边带；其稳定程度依次为：Zn < Cu < Ni < Pb < Cr，其中Zn交换态及碳酸盐结合态比例超过50%，稳定程度极低.而Pb、Cr稳定程度较高，其交换态及碳酸盐结合态比例小于10%.像墨水湖这样受纳高污染负荷市政污水、暴雨径流的城市湖泊，其潜在的重金属生物活性，必须引起足够的重视.     

城市湖泊表层沉积物中的重金属污染现状及其稳定度分析——以武汉墨水湖为例

水体沉积物中的重金属会对生态系统构成直接和间接的威胁.为了研究工业化、城市化过程中城市湖泊沉积物重金属污染程度,以武汉市墨水湖为研究对象,测定了5种重金属Zn、Cu、Ni、Pb及Cr在表层沉积物中的含量,分析了其污染程度、分布特征,并对其稳定度进行了分析.结果表明,墨水湖表层沉积物重金属污染程度较重,在所有采样点5种重金属含量均高于最低效应阈值(LEL),多数采样点甚至超过了严重效应阈值(SEL);该湖泊沉积物中重金属分布具有比较明显的空间差异性:排污口区>湖中心水域>城区岸边带>林田岸边带;其稳定程度依次为:Zn相似文献   

Sources,spatial variation,and speciation of heavy metals in sediments of the Tamagawa River in Central Japan

Sediments of the Tamagawa River in central Japan were studied to explain the spatial variation, to identify the sources of heavy metals, and to evaluate the anthropogenic influence on these pollutants in the river. Sediment samples were collected from 20 sites along the river (five upstream, four midstream, and 11 downstream). Heavy metal concentrations, viz. chromium, nickel, copper, zinc, lead, cadmium, and molybdenum, in the samples were measured using inductively coupled plasma-mass spectroscopy. The chemical speciations of heavy metals in the sediments were identified by the widely used five-step Hall method. Lead isotopes were analyzed to identify what portion is contributed by anthropogenic sources. The total heavy metal concentrations were compared with global averages for continental crust (shale) and average values for Japanese river sediments. The mean heavy metal concentrations were higher in downstream sediments than in upstream and midstream samples, and the concentrations in the silt samples were higher than those in the sand samples. Speciation results demonstrate that, for chromium and nickel, the residual fractions were dominant. These findings imply that the influence of anthropogenic chromium and nickel contamination is negligible, while copper, zinc, and lead were mostly extracted in the non-residual fraction (metals in adsorbed/exchangeable/carbonate forms or bound to amorphous Fe oxyhydroxides, crystalline Fe oxides, or organic matter), indicating that these elements have high chemical mobility. The proportion of lead (Pb) isotopes in the downstream silt samples indicates that Pb accumulation is primarily derived from anthropogenic sources.     

Sources, spatial variation, and speciation of heavy metals in sediments of the Tamagawa River in Central Japan

Sediments of the Tamagawa River in central Japan were studied to explain the spatial variation, to identify the sources of heavy metals, and to evaluate the anthropogenic influence on these pollutants in the river. Sediment samples were collected from 20 sites along the river (five upstream, four midstream, and 11 downstream). Heavy metal concentrations, viz. chromium, nickel, copper, zinc, lead, cadmium, and molybdenum, in the samples were measured using inductively coupled plasma-mass spectroscopy. The chemical speciations of heavy metals in the sediments were identified by the widely used five-step Hall method. Lead isotopes were analyzed to identify what portion is contributed by anthropogenic sources. The total heavy metal concentrations were compared with global averages for continental crust (shale) and average values for Japanese river sediments. The mean heavy metal concentrations were higher in downstream sediments than in upstream and midstream samples, and the concentrations in the silt samples were higher than those in the sand samples. Speciation results demonstrate that, for chromium and nickel, the residual fractions were dominant. These findings imply that the influence of anthropogenic chromium and nickel contamination is negligible, while copper, zinc, and lead were mostly extracted in the non-residual fraction (metals in adsorbed/exchangeable/carbonate forms or bound to amorphous Fe oxyhydroxides, crystalline Fe oxides, or organic matter), indicating that these elements have high chemical mobility. The proportion of lead (Pb) isotopes in the downstream silt samples indicates that Pb accumulation is primarily derived from anthropogenic sources.