北江干流沉积物重金属污染生态风险评价

通过北江干流水体沉积物重金属含量,研究其典型污染物的潜在生态风险。采集了北江干流韶关至清远段7份沉积物样品,经混酸消解后,以电感耦合等离子体质谱仪测定沉积物中重金属含量,并对沉积物重金属分布特征进行了分析。同时利用Hakanson的潜在生态危害指数（RI）评价模式,对北江干流沉积物重金属生态风险进行了评价。评价结果表明,北江干流沉积物中重金属综合生态危害程度均表现为很高级别,其生态危害因子Pb、Cd已成为北江干流突发性水污染事故潜在预警因子。     

芝罘湾表层沉积物中重金属的分布特征及潜在生态危害评价

为了解芝罘湾沉积物中重金属的污染状况,于2009年7月采集了黄海芝罘湾16个站位的表层沉积物并测定了其中的重金属含量.芝罘湾的重金属污染程度较低,所有测定值均低于国家海洋沉积物Ⅰ类质量标准.Hg、Cu、Pb、Cd、Zn、Ni、Co、Mn 8种重金属的平均含量分别为0.02、12.3、8.67、0.13、32.8、11....     

大亚湾表层沉积物中重金属分布特征及潜在生态危害评价

为了解大亚湾沉积物中重金属含量分布及其对海湾生态环境的危害状况,于2006年7月至2007年11月采集了大亚湾10个采样点的春、夏、秋、冬四个季度的表层沉积物样品,分析了沉积物中重金属的含量.结果表明,大亚湾重金属含量均低于海洋沉积物Ⅰ类质量标准,研究海域沉积物中Hg、Pb、Cu、Zn的含量分别为0.009 ～0.158 mg/kg、11.52 ～45.95 mg/kg、2.61 ～64.68 mg/kg、30.58 ～85.07 mg/kg,平均含量分别为0.040、28.50、12.46、61.76 mg/kg,Hg、Pb、Cu的季度差异不明显,Zn有较明显的季节变化.潜在生态危害评价表明,夏季重金属潜在生态危害属于强级污染,其余季节属于中等程度污染;重金属生态危害程度顺序为:Hg＞Cu＞Pb＞Zn,其中Hg的潜在生态危害属于很强级,其余均属于轻微级.     

沱江流域Pb、Cd的环境污染化学行为研究

对沱江流域金堂、简阳、内江三地河流沉积物中重金属Pb和Cd含量及其时空分布特征进行了研究,并结合与沉积物中Fe、Mn和LOI等参数的相关性对河流沉积物中Pb和Cd地球化学性质进行了初步的分析和讨论。结果表明,沱江三地沉积物中Cd、Pb含量不高,平均含量按上、中、下游次序逐渐降低;从垂向分布行为看,Cd在上游金堂地区上部含量高于下部,而中、下游两地则相反,而Pb均随着深度的增加而减少,反映了近年来人类活动所产生Pb污染的加剧;TOC、沉积物性状和上覆水体中的物化性质对于其垂向分布有着较大影响。对于深入揭示水环境中重金属的环境地球化学循环有着重要的指导意义。     

象山港沉积物对重金属Fe和Mn的吸附特征

对象山港不同站点的沉积物对重金属铁、锰的吸附特征进行了研究,考察了阳离子交换量、有机质含量对铁、锰的吸附能力的影响。吸附动力学实验表明,沉积物对铜和锌的吸附量随着铁、锰的初始含量增加而增大,但分别都在40 min和30 min左右达到吸附平衡;热力学实验结果表明,不同沉积物对铁、锰的热力学吸附过程符合Freundlich等温方程,各站点沉积物对铁的吸附能力由强到弱依次是S02,S25,S17,S10,S12,D03,D08,各站点沉积物对锰的吸附能力由强到弱依次是S02,S25,S17,S12,S10,D03,D08;影响因素实验表明,有机质的含量是影响沉积物对重金属铁吸附能力的主要影响因素之一,而沉积物对锰的吸附能力与阳离子交换量存在一定的关联性,有机质的含量几乎不影响沉积物对锰的吸附能力。因此,沉积物对重金属铁、锰的吸附系数K并不与其中单个理化性质有明显的相关性,这说明沉积物对铁、锰的吸附强度受多种沉积物理化性质控制。     

潮州市西湖沉积物中金属元素的污染特性研究

用原子吸收分光光度法研究了潮州市西湖沉积物中的铜、锌、铅、镉、锰、镍、镁、钙等金属元素的含量及分布规律。结果表明,铜、铅、锌、镉和镍是主要的重金属污染物,沉积物中5种重金属的平均含量为:铜584.7 mg/kg,铅149.1 mg/kg,锌360.9 mg/kg,镉1.2 mg/kg,镍76.7 mg/kg,均高于我国土壤背景值。     

万宁小海表层沉积物中重金属物质的空间分布特征及生态风险分析

为了解万宁小海海域表层沉积物重金属污染状况,2020年5月在小海潟湖采集18个沉积物样品,采用电感耦合等离子体质谱法（ICP-MS）同时测定5种重金属含量,采用原子荧光光度计测定总汞和砷,并分析归纳出重金属分布特征。采用Hakanson的潜在生态风险指数法识别小海表层沉积物潜在生态风险程度,以及运用富集系数和地累积法进一步评价小海表层沉积物重金属的污染程度。结果表明：Cu、Pb、Zn、Cd、Cr、Hg和As含量平均值分别为7.26 mg/kg、27.08 mg/kg、75.06 mg/kg、0.16 mg/kg、38.43 mg/kg、0.054 mg/kg、4.66 mg/kg,均符合第一类海洋沉积物质量标准。7种元素的潜在生态风险程度依序为Hg＞Cd＞Pb＞As＞Cu＞Cr＞Zn,其中Hg和Cd为主要潜在生态危害因子,其综合潜在生态风险等级已达到中等级风险;富集系数评价和地质累积系数评价污染程度依次为：Cd＞Hg＞Pb＞Zn＞Cr＞As＞Cu;表层沉积物中TOC 含量与 Cu、Pb、Zn、Cd 和 Cr 含量具存在显著正相关,与粒度呈一定的负相关。     

火焰原子吸收光谱法分析沉积物中重金属元素的形态

采用原子吸收光谱法研究了金沙江攀枝花段水系沉积物中重金属的形态及分布特征。研究发现,各重金属的形态以残渣态为主,离子交换态含量很少。同时说明原子吸收光谱法完全可以用来研究重金属形态特征,在环境研究中具有重要意义。     

自动消解仪—ICP法测定水系沉积物中6种重金属元素

建立了自动消解仪-电感耦合等离子体发射光谱法(ICP-OES)同时测定水系沉积物中Cu、Zn、Ni、Cr、Pb、Co六种元素含量的方法。该方法的相关系数好、检出限低。方法经国家标准物质(GBW07361)验证,准确度和精密度均能达到环境监测分析的要求,为水系沉积物中重金属元素含量的测定提供了简单可靠的分析方法。     

沉积物中重金属形态分析方法研究进展

介绍近年来国内外对沉积物中重金属的研究概况,以及重金属形态分离方法和监测方法的最新进展,对国内外常用的沉积物中重金属的形态分析提取方法如Tessier法、Forstner法和BCR法进行了比较,概述了重金属形态分离检测方法。     

Voltammetric method for the determination of Zn,Cd, Pb,Cu and Ni in interstitial water

To determine heavy metals in interstitial water from Baltic sea sediments a sampling method with subsequent voltammetric determination is described. Copper, lead, zinc and cadmium are determined in the UV-digested samples of interstitial water by differential pulse anodic stripping voltammetry while nickel is determined by adsorption voltammetry. The determination of five metals in one sample in a wide concentrations range is possible using a low cost apparatus. The profiles of the metal concentrations in interstitial water of subsequent layers of sediments, sampled from Puck Bay, Gdańsk Bay, the Bornholm area and the S?upsk area are presented.     

Contents of some heavy metals in plants from Saginaw Bay (Lake Huron) and some small lakes in wilderness areas of Michigan's Upper Peninsula as analyzed by neutron activation analysis

Our results indicate that the highest concentrations of heavy metals occurred in those plants collected near the mouth of the Saginaw River. The alga, Cladophora sp., and the flowering plant, Typha augustifolia (cat-tail), are notable for the high concentration of heavy metals that they accumulated. In addition, several other species that were sampled from small lakes in Michigan's Upper Peninsula contained higher concentrations of certain metals (Ba, Cr, Rb) than from any samples obtained from Saginaw Bay. Different organs of the same species, or of the same plant, such as cat-tail, vary widely in concentrations of the same elements. A computer-derived analysis of our data is presented, and the implications of our results as they relate to pollution by heavy metals in fresh-water lakes is discussed. This work was supported by a private subsidy from Edna Newnan, Bloomfield Hills, Michigan to whom we express our thanks for hernerous support. We also wish to thank the Division of Biological Sciences, The University of Michigan, for making funds available for the computer analyses performed in this study.     

北部湾文蛤体内氧化逆境标志物对重金属积累的响应研究

研究目的是通过评价北部湾文蛤（Meretrix meretrix）体内7种氧化逆境标志物对重金属积累的响应, 筛选出能够灵敏指示海域现场重金属污染压力的生物标志物. 2011年秋季, 在北部湾沿海潮间带6个典型站位采集文蛤样品, 测定软组织中重金属含量及鳃、内脏中7种氧化逆境标志物水平, 分析其空间、组织分布特征, 然后对标志物水平与重金属含量进行相关性分析. 结果表明, 文蛤软组织中重金属积累量和氧化逆境标志物水平在站位间存在很大差异. 大多数氧化逆境标志物具有明显的组织差异性, 鳃中的超氧化物歧化酶（SOD）、谷胱甘肽过氧化物酶（GPx）、谷胱甘肽转硫酶（GST）活性以及还原型谷胱甘肽（GSH）、氧化型谷胱甘肽（GSSG）含量均高于内脏, 过氧化氢酶（CAT）在内脏中的活性较高, 而硫代巴比妥酸反应物（TBARs）在两组织中无明显的分布差异. 多种重金属共存的情况下, 鳃的GSH/GSSG与软组织Cd含量有显著相关性; 4种抗氧化酶中, 鳃CAT对Pb具有显著正响应, 内脏CAT、GST对As具有显著负响应. 鳃TBARs分别与Hg、Cd含量呈显著正相关、负相关, 内脏TBARs则与Pb含量呈负相关, 表明这些标志物能够灵敏指示重金属对文蛤抗氧化防御机能的影响, 适于作为评价北部湾重金属污染压力的指标.     

Heavy Metal Concentrations in Water,Sediment and Fish from Izmit Bay,Turkey

Abstract

Mercury, cadmium and lead levels in water, sediment and fish samples from Izmit Bay, Turkey have been determined. Sampling and analysis methods are described. Variations of heavy metal concentrations from different sampling stations are discussed. Results indicate that the levels of mercury and cadmium were highest in the vicinity of a chlor-alkali plant while the highest concentration of lead was near a metallic pipe factory. The amounts of heavy metals found in the shoreline sediment samples were similar to those found in fish species from the bay.     

Voltammetric method for the determination of Zn, Cd, Pb, Cu and Ni in interstitial water

To determine heavy metals in interstitial water from Baltic sea sediments a sampling method with subsequent voltammetric determination is described. Copper, lead, zinc and cadmium are determined in the UV-digested samples of interstitial water by differential pulse anodic stripping voltammetry while nickel is determined by adsorption voltammetry. The determination of five metals in one sample in a wide concentrations range is possible using a low cost apparatus. The profiles of the metal concentrations in interstitial water of subsequent layers of sediments, sampled from Puck Bay, Gdask Bay, the Bornholm area and the Supsk area are presented.     

固相微萃取-气质联用测定胶州湾海水中有机锡化合物

采用顶空固相微萃取-气质联用(HS-SPME-GC-MS)技术测定了胶州湾海水中有机锡的含量.样品用4%的四乙基硼化钠(NaBEt4)进行衍生,同时用PDMS纤维进行萃取,萃取富集后,用气质联用仪进行测定.通过分析,该方法中MBT的线性范围为10～1000ng/L,DBT和TBT的线性范围为50～1000ng/L,相对标准偏差低于14.0%,回收率在70.0%～125.0%之间,检出限低于12.5ng/L;通过所建立的方法对胶州湾海水中有机锡的污染现状进行了调查,发现胶州湾海水中存在不同程度的有机锡污染.     

Determination of trace PAHs in seawater and sediment pore-water by solid-phase microextraction (SPME) coupled with GC/MS

A fast and reliable method for the determination of trace PAHs (polynuclear aromatic hydrocarbons) in seawater by solid-phase microextraction (SPME) followed by gas chromatographic (GC) analysis has been developed. The SPME operational parameters have been optimized, and the effects of salinity and dissolved organic matter (DOM) on PAHs recoveries have been investigated. SPME measures only the portion of PAHs which are water soluble, and can be used to quantify PAH partition coefficient between water and DOM phases. The detection limits of the overall method for the measurement of sixteen PAHs range from 0.1 to 3.5 ng/g, and the precisions of individual PAH measurements range from 4% to 23% RSD. The average recovery for PAHs is 88.2±20.4%. The method has been applied to the determination of PAHs in seawater and sediment porewater samples collected in Jiaozhou Bay and Laizhou Bay in Shandong Peninsula, China. The overall levels of PAHs in these samples reflect moderate pollution compared to seawater samples reported elsewhere. The PAH distribution pattern shows that the soluble PAHs in seawater and porewater samples are dominated by naphthalenes and 3 ring PAHs. This is in direct contrast to those of the sediment samples reported earlier, in which both light and heavy PAHs are present at comparable concentrations. The absence of heavy PAHs in soluble forms (<0.1-3.5 ng/L) is indicative of the strong binding of these PAHs to the dissolved or solid matters and their low seawater solubility.     

Lead,cadmium, and arsenic in commercial algae of the Sea of Japan

The concentrations of toxic elements (arsenic, cadmium, lead) in commercial algae Saccharina japonica and Ahnfeltia tobuchiensis from different habitats of the Sea of Japan have been determined. Bioaccumulation of heavy metals has been analyzed with respect to the habitat and growth conditions. The lead content of Sascharina japonica from all habitats and arsenic content of the same alga species from the Ol’ga Bay, Kievka Bay, and Tatar Strait have been found to exceed maximum permissible levels. Increased lead concentrations have been detected in Ahnfeltia tobuchiensis. Samples of Ahnfeltia tobuchiensis collected from the bottom layer contain more toxic elements than those from the upper layer.