大亚湾海域典型有机氯农药生物累积特征及变化因素研究

于2003年采集大亚湾海域28个鱼类等生物样品和14个表层沉积物样品,分析其中滴滴涕(DDTs)、六六六(HCHs)和氯丹(CHLs)各组分的含量以及脂含量和δ15N,δ13C同位素值,重点研究了大亚湾沉积物和生物体中有机氯农药(OCPs)的污染现状及其生物积累规律.大亚湾海域鱼类DDTs,HCHs和CHLs平均含量分别为57.1±52.9,0.30±0.18和0.87±0.35ng/g(湿重);与其他海区相比,该海域生物体中DDTs的含量相对较高,HCHs和CHLs较低;表层沉积物中高的p,p'-DDT含量及较低的(DDE+DDD)/DDT比值(平均为0.56,<1),均显示仍有新的DDTs源输入;OCPs在生物累积中表现出脂溶性的特征,生物体内脂含量越高,其OCPs含量也越高;δ15N,δ13C同位素的研究结果显示肉食性生物比植食性生物更易累积OCPs;大亚湾海域OCPs的生物-沉积物累积系数(BSAF)与有机物的亲脂性程度即辛醇-水比值(K_OW)存在显著的正相关.     

三沙湾表层沉积物中有机污染物的含量及风险评价

利用气相色谱/质谱方法对三沙湾表层沉积物中多氯联苯(PCBs)、多环芳烃(PAHs)和有机氯农药(OCPs)进行测定,结果表明,PCBs、PAHs和OCPs的含量均值分别为1.28、61.76和1.18ng/g。与早期研究结果相比,PCBs含量浓度明显降低,表明其污染已得到有效控制;PAHs中高分子量组分普遍存在,通过分析菲/蒽和荧蒽/芘比值,判断其主要来源为燃料的高温燃烧;HCHs和DDTs是主要的有机氯农药污染物,二者的残留特征表明其主要来源为早期历史残留,且表层沉积物受到厌氧微生物降解。总体而言,三沙湾表层沉积物中PCBs、PAHs和OCPs的污染程度及生态风险均处于较低水平。     

西北太平洋海域黑潮区有机氯农药和多氯联苯的浓度及其组成特征

由于传统持久性有机污染物（POPs）如有机氯农药（OCPs）和多氯联苯（PCBs）在全球范围内被广泛的限制或禁用,各种环境介质中的污染物浓度呈现逐年降低的趋势。西北太平洋作为远离大陆的开放性海域,无明显的污染点源,其洋流在POPs的输送和扩散过程中扮演重要的角色。本研究采集西北太平洋黑潮区表层和次表层（2～5 m和150 m）水体为研究对象,分析其中溶解态OCPs（六六六（HCHs）、滴滴涕（DDTs）、氯丹（CHLs））和PCBs的浓度及组成特征。结果显示,黑潮区表层水体中HCHs、 DDTs、 CHLs和PCBs的浓度范围分别为30.7～68.8 pg/L、 6.16～23.8 pg/L、1.07～5.75 pg/L和49.8～124 pg/L;次表层水体中分别为27.3～68.4 pg/L、7.06～14.1 pg/L、0.518～10.1 pg/L和34.1～68.4 pg/L。HCHs各异构体的比值特征表明该海域以林丹输入为主,而DDTs和CHLs的比值结果显示,该海域水体中滴滴涕和氯丹均主要是来自于历史残留。水体中PCBs主要以三氯联苯、四氯联苯为主,与东亚多氯联苯的历史使...     

桑沟湾水体中有机氯农药和多氯联苯的浓度水平及分布特征

以气相色谱-电子捕获检测器(GC/ECD)分析并结合外标法,定量测定了桑沟湾海域水体中15种有机氯农药和多氯联苯类化合物的含量.结果表明:桑沟湾海域表层水体中有机氯农药浓度范围为20.34～52.86 ng/L,底层水中的浓度范围为31.7～58.68 ng/L.该海域水体中共检出有机氯农药6种,DDTs类化合物是水体...     

大亚湾海域水体和沉积物中多环芳烃分布及其生态危害评价

1999年8月首次采集大亚湾海域14个站位的次表层水和表层沉积物样品,分析其中16种多环芳烃(PAHs)单体的含量,探讨其可能的来源,并进行典型有机污染物生态危害评价。结果表明,海水中PAHs平均含量为10984±8461ng·L-1,变化范围为4228—29325ng·L-1;表层沉积物中PAHs平均含量为481±316ng·g-1,变化范围为115—1134ng·g-1;大亚湾海域PAHs含量比其它近岸海区相对较高。PAHs的组成在水体中以3环为主,在沉积物中以4环为主。菲/蒽和荧蒽/芘比值显示沉积物中PAHs来自化石燃料的燃烧和成岩作用的输入。PAHs在沉积物/水中的富集系数平均值为72,变化范围为9—756。大亚湾海域水体PAHs污染严重而表层沉积物污染较轻,显示尚有较大量的PAHs输入。为保持大亚湾海洋生态系统的可持续发展,必须加强PAHs的监测,特别是生物体中PAHs含量的分析。     

大连湾和杭州湾表层沉积物中多氯联苯和有机氯农药及风险评价

对大连湾与杭州湾沉积物样品中多氯联苯(Polychlorinated Biphenyls,PCBs)和有机氯农药(Organochlorine Pesticides,OCPs)进行了分析测定。结果表明,大连湾和杭州湾沉积物中PCBs的含量为0.72~14.87 ng/g和0.76~3.86 ng/g,其中3、4、5氯联苯比例较高,其和超过总含量的70%;OCPs的含量为2.98~32.23 ng/g和1.61~4.71 ng/g,其中主要成分为六六六(Hexachlorocyclohexanes,HCHs)和滴滴涕(Dichlorodiphenyldichloroethylenes,DDTs)。大连湾和杭州湾表层沉积物中HCHs主要来自农业使用,而且大连湾有新的DDTs输入,杭州湾表层沉积物中的DDTs则主要来自历史残留。生态风险评价的结果表明,PCBs几乎不会对研究区域产生生态风险,OCPs对杭州湾也不会造成潜在的生态风险,但大连湾的OCPs处于中等风险水平,应当引起关注。     

桑沟湾水体中有机氯农药时空分布特征

利用气相色谱法分析并结合外标法,定量测定2009年4个航次桑沟湾海域水体中8种有机氯农药的质量浓度,探讨了有机氯污染物在该海域组成以及时空分布特征。结果表明,DDTs类农药是桑沟湾水体中主要的有机氯农药种类。该海域有机氯农药质量浓度分布特征呈现8月份较高,10月和12月份次之,4月份最低。与其他海域相比,其有机氯农药质量浓度处于中等水平。桑沟湾的水体中HCHs和DDTs质量浓度均符合国家一类海水质量标准。     

厦门海域表层沉积物中DDTs、HCHs和PCBs的含量及其分布

对厦门海域表层沉积物中有机氯农药和多氯联苯的含量与分布进行了调查研究.调查结果表明厦门海域HCHs和PCBs含量较低,远低于国家海洋沉积物质量标准第一类底质标准的阈值,说明其污染已受到有效控制;但厦门海域表层沉积物中DDTs含量较高,部分海区已经超出或者接近国家海洋沉积物质量标准第一类底质标准的阈值.DDTs和PCBs有极为相似的分布特征,而HCHs的分布特征则不尽相同.     

桑沟湾水体及沉积物中有机磷农残时空分布特征

以气相色谱-质谱法(GC-MS)分析并结合外标法,定量测定了2009年4月—2010年2月6个航次桑沟湾海域水体和沉积物中常见的8种有机磷农药,探讨了该海域有机磷农药组成以及时空分布特征.结果表明:桑沟湾水体中共检出有机磷农药6种,其中甲基对硫磷、马拉硫磷和对硫磷等3种有机磷农药在各航次均有检出.沉积物中有机磷农药含量的水平分布呈现由湾口向湾内海域逐渐降低的趋势.该海域水体中有机磷农药含量呈现10月份较高,4月、6月和8月份次之,12月和 2月份最低的月份分布特征.与国内外类似水体相比,桑沟湾海域中总有机磷农药含量处于轻度污染水平,甲基对硫磷、马拉硫磷等单组分含量也处于较低水平.     

中国北部辽东湾表层沉积物中PAHs源解析和生态风险评价

研究于2014年和2015年对辽东湾表层沉积物中16种多环芳烃（PAHs）的来源和生态风险状况进行了调查和评估。辽东湾表层沉积物中16种PAHs的含量范围为88.5-347 ng/g,高值区主要分布在辽东湾中部海域。对辽东湾各站位沉积物中多环芳烃的含量进行中聚类分析结果表明,辽东湾的采样站位可分为两类,一类站位主要分布在辽东湾沉积物中部海域,另一类站位主要分布在受陆源污染较为严重的近岸海域。辽东湾表层沉积物中PAHs的来源为燃烧源和石油源的混合来源,其中燃烧源为主要来源。萘、苊、苊烯、菲、二苯并[a,h]蒽可能偶尔会引发有害生物效应;辽东湾表层沉积物为低致癌风险;辽东湾中部海域表层沉积物中PAHs的生态风险和毒性污染水平高于辽东湾近岸海域。     

Distribution and sources of organochlorine pesticides in water and sediments from Daliao River estuary of Liaodong Bay,Bohai Sea (China)

The levels of 19 kinds of organochlorine pesticides (OCPs) in the aqueous phase, suspended particulate matter (SPM), pore water and sediments from Daliao River estuary of Liaodong Bay (Bohai Sea) in northeast China were investigated to evaluate their potential pollution risks. The total OCPs concentrations in the aqueous phase, SPM, pore water and sediments were 3.7–30.1 ng l⁻¹, 4.6–52.6 ng l⁻¹, 157–830 ng l⁻¹ and 2.1–21.3 ng g⁻¹ dry weight, respectively. The concentrations of OCPs, in the Daliao River estuary, are in the mid-range, as compared to those reported in other estuaries worldwide. The distribution of HCHs and DDTs were different indicating different contamination sources. Lindane is the main type of HCH and continuing use in northeast China of ‘pure’ HCH (lindane) rather than technical HCH accounts for the source. The ratios of (DDE + DDD)/DDT in the samples indicate no recent inputs of these chemicals to the estuary.     

连云港西大堤海域水环境污染特征分析

连云港拦海西大堤建成已20余年,为得到近几年来本海域水环境中重金属和有机污染物的污染特征,作者于2011年6月对海州湾西大堤海域进行现场调查,根据海洋监测规范对采集水样的DO、COD、石油、重金属(Cu、Zn、Pb、Cd)、活性磷酸盐、无机氮9个化学指标进行测定,并对水质现状进行评价。同时,本研究测定了连云港海州湾西大堤近岸表层沉积物中多种重金属和有机质的含量,利用因子分析法研究了沉积物中重金属的污染来源。结果表明:海州湾西大堤海域海水中重金属Cu、Zn、Pb、Cd的平均质量浓度皆未超出国家二类海水水质标准,石油类和无机氮类污染物为本海域海水中的首要污染物,有机物污染呈现加重的趋势。表层沉积物中重金属Zn、Cd、As的富集指数大于3,属于重污染级别。根据数理统计,发现前3个主成分的贡献率分别为44.09%、27.61%、13.44%,表明沉积物重金属主要有3个来源:工业和生活污水排放、港口煤渣倾倒、海陆交通排污。     

近50年长江口的主要有机污染的记录

本文通过近50年来我国长江口及长江流域有机物污染物的研究记录和成果和国内外其它重要河口海域的资料进行对比分析,认为人类近50年的活动对长江口已造成了比较严重的有机污染。本世纪初长江干流中检出的有机污染物达308种。从上世纪50年代到80年代初长江口的有机氯农药污染呈逐年上升趋势,之后开始下降,但至今还对生态系统造成影响。同时,与上世纪80年代相比,上个世纪90年代长江口的多氯联苯(PCBs)污染要来得重。在上世纪50年代和60年代在我国沿海均已出现油污染,并在上世纪90年左右最为严重,虽然从上世纪90年代中期开始呈下降趋势。长江口多环环芳烃(PAHs)污染在上世纪70年代很少,但随着长江流域工业的发展,从上世纪80年代开始加重,到上世纪90年代中期才开始下降。     

Trace organic contaminants and their sources in surface sediments of Santa Monica Bay,California, USA

Spatial distribution of selected contaminants in the surface sediments of Santa Monica Bay (SMB), California was investigated. Sediments were analyzed for DDTs (DDT and metabolites), polychlorinated biphenyls (PCBs), polycyclic aromatic hydrocarbons (PAHs), linear alkylbenzenes (LABs) and coprostanol. Effluent samples from the Hyperion Treatment Plant (HTP), which discharges treated municipal wastewater effluents into SMB, were also analyzed. The inter-correlation in the distribution trends of contaminants was examined. The concentrations of contaminants were interpolated in a geographic information system to visualize their spatial distribution in the Bay. Inventories of the contaminants were also estimated.The concentrations of coprostanol, LABs and PCBs are very high only in the vicinity of the sewage outfall whereas PAHs and DDTs occur widespread in the Bay. The poor correlation of DDTs with LABs, PAHs or coprostanol content confirms the historic origin of DDTs and their absence in the contemporary wastewaters. Moderate correlation of DDTs with PCBs implies historic deposits as a major origin of PCBs. There are hot spots of DDTs at water depths of 60 and 100 m and the inventory of DDTs in Bay sediments is insignificant compared to that estimated in the Palos Verdes Shelf which extends from the southern edge of Redondo Canyon around Palos Verdes Peninsula. The concentration of toxic contaminants was examined according to published sediment quality guidelines. About 20 stations contain p, p′-DDE and/or total DDTs above ERM and, PCBs between ERL and ERM indicating potential for adverse biological effects.     

厦门港湾沉积物中有机氯农药和多氯联苯的垂直分布特征

从厦门港海区采集两根沉积柱样，研究有机氯农药六六六（ＨＣＨｓ），滴滴涕（ＤＤＴｓ）和多氯联苯（ＰＣＢｓ）在沉积物中的垂直分布，ＨＣＨｓ，ＤＤＴｓ及ＰＣＢｓ含量用ＧＣ法测定，取自厦门港湾口的１号柱样ＨＣＨｓ，ＤＤＴｓ和ＰＣＢｓ的含量范围分别为０．１２～ ０．３２ｎｇ／ｇ，４．６４～１０．５ｎｇ／ｇ和０．０９～０．４６ｎｇ／ｇ取自厦门西港内湾的５号柱样采分别为０．１７～０．３１ｎｇ／ｇ，３．６５     

Can salt marsh plants influence levels and distribution of DDTs in estuarine areas?

Sediments are depositories of toxic substances such as organochlorine pesticides and there is a global need for their removal in contaminated environments. Studies that combine contaminated sediments and phytoremediation are relatively recent and their number has been increasing. This work aimed to investigate whether salt marsh plants (sea club-rush Scirpus maritimus, sea rush Juncus maritimus and sea purslane Halimione portulacoides) can favor DDT and metabolites remediation in estuarine environment. For this purpose the levels of DDT, DDE and DDD were compared in vegetated and non-vegetated sediments from an estuary in the North of Portugal (in-situ study) and from another in the South of Portugal (ex-situ study). Results obtained both in the in-situ study, involving S. maritimus and J. maritimus, and in the ex-situ study, involving H. portulacoides, indicated that these plants did not have a significant role in DDTs removal and/or degradation. Therefore, it seems that the tested plants cannot influence levels and distribution of DDTs in estuarine areas.     

The PAH composition of surface sediments from Stagnone coastal lagoon, Marsala (Italy)

This paper examines the presence, distribution, nature and sources of 22 Aromatic Hydrocarbons (PAHs), which are important environmentally and toxicologically, in sediments from the Stagnone coastal lagoon at Marsala (Italy). Analysis was performed by gas chromatography/mass spectrometry (GC/MS) with selected ion monitoring (SIM). The total concentration of polycyclic aromatic hydrocarbons ranged from 72 to 18381 μg/kg of dry matrix. The relative standard deviation (RSD) of the replicates on the concentrations of individual compounds ranged from 5% to 20%. The accuracy of method was estimated by analyzing “blank” samples added of known quantities of analytes and the recover percentage was 88 ± 9%. The detection limit (LOD) of analytical procedure was less than 0.2 μg/kg d.w. for all analytes. The quantification limit (LOQ) of analytical procedure was less than 0.7 μg/kg d.w.The resulting distributions and weight ratios of specific compounds are discussed in terms of sampling location and origin of organic matter. A comparison with other studies of total PAHs suggests that the levels are within the concentration ranges already reported by other authors. From an eco-toxicological point of view, total PAH concentrations at seven out of the eight sites studied represent a relatively clean environment when compared to other sites.Organic matter content and PAH concentrations were found to be correlated and the compounds present in Stagnone sediments were shown to be mainly of pyrolitic origin, while a negligible quantity of PAHs may derive from biogenic sources since all the sediments contain perylene traces. There is no evidence of coal-tar contamination.Cluster analysis was carried out in order to discriminate between different PAH origins.