钦州湾海水中石油烃时空变化特征及其影响因素

2009年1月至11月对广西钦州典型养殖海湾-钦州湾海域表层海水石油烃进行了4次采样调查,分析该海域石油烃污染状况,探讨石油烃的时空分布特征及其影响因素。结果表明,钦州湾表层海水石油烃的质量浓度在0.001~0.095 mg/L之间,平均值为0.022 mg/L;季节变化呈现夏季最高,秋、冬季次之,春季最低的特点,夏、冬季海水受到不同程度石油污染,春、秋季均达到国家《海水水质标准》二类标准。水平分布上总体呈现春、秋季节外湾大于内湾,夏、冬季节内湾大于外湾的特征。钦州湾水产养殖活动及陆地径流输入是影响石油烃时空变化的主要因素。春季石油烃的质量浓度与温度和溶解氧等环境因子有着较好的相关性,夏季石油烃和溶解无机磷存在显著正相关。总体上钦州湾海域目前受石油烃污染程度较轻,仍有一定接纳自净能力。     

胶州湾海水中阴离子表面活性剂的含量及分布

根据2003年5月和8月对胶州湾进行的两次现场调查，采用亚甲基蓝分光光度法测定了该海域海水中阴离子表面活性剂含量并初步分析了其分布特点。结果表明，2003年5月胶州湾全湾表层海水中阴离子表面活性剂平均浓度为12．6μg／L，略高于8月份(10．3μg／L)；各站位含量有变化，河口及邻近海域站位高于其他站位；表层海水含量高于底层海水。     

威海双岛湾海域重金属的分布特征及生态风险评价

根据2012年双岛湾海域环境调查资料,研究了海水和表层沉积物中重金属的分布特征以及生态风险。结果显示,双岛湾海域海水中的重金属Cu和Pb在湾中部和湾底的部分站位含量较高,Zn和Cr含量在湾底最高、湾外最低,Cd和Hg在湾底和湾外的含量均高于湾中部,As的分布比较均匀;除Zn和Pb外,其余重金属含量均高于周边其他海域。双岛湾海域沉积物中重金属含量较低,与区域背景值相近,其中重金属Hg和Cd在湾内沉积作用明显,而Cu、Pb和Cr在湾外沉积作用比较明显。相关性分析表明,有机碳含量对双岛湾沉积物中的重金属分布影响不大。生态风险评价结果表明,双岛湾海域海水未受到重金属的污染;表层沉积物中重金属存在中低度的生态风险,具有潜在的不利生物毒性效应,重金属毒性大小依次为Pb>As>Cu>Hg>Cr=Cd>Zn。     

泉州湾表层水主要化学要素含量和富营养化指数的时空变化特征

根据泉州湾2010年4个航次的现场调查资料,分析泉州湾表层海水中化学需氧量、无机氮、活性磷酸盐含量的季节变化特征,应用海湾富营养化评价模式对泉州湾海域海水富营养化状态进行评价,得出秋季和冬季富营养化指数（17.85和18.32）相对较高,夏季和春季富营养化指数（3.02和5.89）相对较低,与无机氮、活性磷酸盐含量的季节变化特征相似.根据近20 a泉州湾海域历史监测数据得出富营养化指数年际变化特征呈现先缓慢升高,后下降,最后又升高的趋势,与无机氮、活性磷酸盐的年均含量变化特征基本相似,近几年来富营养化指数（14.57）急剧增大,表明泉州湾海水富营养化程度非常严重.泉州湾海水富营养化指数平面分布特征总体上呈现由湾口向晋江入海口、后渚附近海域逐渐递增的趋势,与无机氮含量平面分布特征一致,与活性磷酸盐含量平面分布特征相似.     

泉州大港湾海水、沉积物及水产生物体内重金属的含量分布

根据1997年7月大港湾海域环境调查资料,着重分析了大港湾海水、表层沉积物及水产生物体内重金属的含量及分布。结果表明：大港湾海水中Cu,Pb,Cd,Zn的含量均低于渔业水质标准,大港湾湾顶水域,海水和表层沉积物中Cu,Pb,Cd,Zn的含最明显高于湾口水域：湾南部水域高于北部水域。文中还根据《海洋沉积物质量》、《无公害食品》、《食品中锌限量卫生标准》、《海洋生物质量》标准对表层沉积物和6种水产生物的重金属污染程度进行评价,结果大港湾的水产生物体内的重金属含量均未超标,但沉积物中的Cd含量已超标。     

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。     

兴化湾表层海水和沉积物中重金属含量的时空变化特征

根据福建兴化湾2006年12月（冬季）和2007年4月（春季）表层海水以及2007年3月表层沉积物的监测资料,分析了该海域表层海水和沉积物中重金属Cu、Pb、zn、Cd、Hg和As含量的时空变化特征,评价了该海域重金属的污染程度．结果表明：冬季,调查海域表层海水中cu、Pb、zn、cd、Hg、As的含量范围分别为〈0．20～2．42、〈0．03～1．08、〈3．1～16．5、〈0．010—0．043、〈0．007～0．170、0．82～4．00肌g／dm’;春季其含量范围分别为0．91～3．80、0．18～3．40、8．7～36．0、〈0．Ol～0．22、〈0．007～0．063、0．63～1．58~g／dm’．这两季表层海水重金属的测值均低于《海水水质标准（GB3097—1997）》第二类标准值,其中春季cu、Pb、zn、cd含量的均值高于冬季,可能与陆源重金属污染物入海的影响有关．兴化湾表层沉积物中cu、Ph、zn、Cd、Hg和As的含量范围分别为7．60～22．oo、22．4～39．1、54．2～114．0、0．045～0．082、0．020～0．066、5．00～10．20mg／kg,均低于《海洋沉积物质量（GB18668_2002）》的第一类标准值．该湾表层海水和沉积物中重金属含量的平面分布特征呈近岸海域较高．此外,对其历年来监测结果的比较表明,兴化湾表层海水和沉积物中cu和Ph含量的多次监测值较接近,但重金属zn含量的监测值存在着波动现象．     

兴化湾表层海水氮磷营养盐含量的时空变化及富营养化状况

根据福建兴化湾海域2006年12月（冬季）和2007年4月（春季）的水质监测资料,分析了表层海水无机氮和活性磷酸盐含量的时空变化特征,并对该海域表层水体的富营养化状况进行了评价.结果表明,冬、春两季,兴化湾表层海水无机氮含量的变化范围分别为0.30~1.30、0.34~1.10mg/dm3,均值分别为0.50、0.54 mg/dm3;无机氮的单项污染指数变化范围分别为1.0~4.2、1.1~3.7,均值分别为1.7和1.8.冬、春两季,其海水活性磷酸盐含量的变化范围分别为0.024~0.085、0.016~0.148 mg/dm3,均值分别为0.040、0.038 mg/dm3;其单项污染指数变化范围分别为0.8~2.8、0.5~4.9,均值则都为1.3.其次,该湾表层海水无机氮和活性磷酸盐含量的空间分布特征为西侧近岸水域的较高,往湾口方向递减.冬、春两季兴化湾表层海水富营养化指数（E值）分别为3.53和4.26,基本呈现富营养状态;富营养化严重的区域主要位于兴化湾西南部,其E值最高达29.9.     

兴化湾海域水体和表层沉积物中重金属分布及其源解析

根据2015年春季兴化湾海域的环境调查资料,对海水和沉积物中的重金属分布及其来源进行了探讨。采用单因子污染指数法和地质累积指数法对海水和沉积物污染程度进行评价,并利用主成分分析法对其重金属的潜在来源进行解析。结果显示:表层海水中重金属Cd,As和Cr质量浓度符合海水水质一类标准,重金属Cu,Pb,Zn,Hg质量浓度均符合海水水质二类标准;表层沉积物中重金属Cu,Pb,Zn,Hg,As,Cd,Cr含量均符合海洋沉积物质量一类标准。地质累积指数评价结果显示,沉积物中重金属Cd总体为污染,其余6种重金属为清洁水平。表层沉积物中重金属间相关性分析表明,Hg与Cu,Zn之间具有相似的来源特征。研究区重金属潜在来源主要为江阴港周边入港船舶排放、生活污水和工农业生产的输入、周边河流输入和大气沉降等。     

桑沟湾海域石油烃的分布特征及其与环境因子的相关性

2009-04-2010-02对山东荣成典型养殖海湾-桑沟湾海区表层海水的石油烃进行6个航次的监测,分析该海区石油烃的污染现状,探讨石油烃在桑沟湾表层海水中的分布特征,以及与水温、叶绿素a、营养盐等环境因子的相关性.结果表明,桑沟湾表层海水石油烃质量浓度的季节变化大致呈现春夏季高,秋季偏低,冬季最低的特点;水平分布基本...     

Evidence for enhanced bioavailability of trace elements in the marine ecosystem of Deception Island, a volcano in Antarctica

This study assessed whether trace elements present at Deception Island, an active submarine volcano in the Antarctic Peninsula, show enhanced biological availability to the local marine community. Using a weak acid extraction method to dissolve organic material and leach associated but not constitutive trace elements of sediments, fifteen elements were measured from seafloor sediment, seawater particulates, and tissues of benthic (bivalves, brittlestars, sea urchins) and pelagic (demersal and pelagic fishes, krill) organisms collected in the flooded caldera. The highest element concentrations were associated with seafloor sediment, the lowest with seawater particulates and organism tissues. In the case of Ag and Se, concentrations were highest in organism tissue, indicating contamination through the food chain and biomagnification of those elements. The elements Al, Fe, Mn, Sr, Ti, and to a lesser extent Zn, were the most concentrated of the trace elements for all sample types. This indicates that the whole ecosystem of Deception Island is contaminated with trace elements from local geothermal activity, which is also reflected in the pattern of element contamination in organisms. Accordingly, element concentrations were higher in organisms collected at Deception Island compared to those from the neighboring non-active volcanic King George Island, suggesting that volcanic activity enhances bioavailability of trace elements to marine organisms. Trace element concentrations were highest in digestive tissue of organisms, suggesting that elements at Deception Island are incorporated into the marine food web mainly through a dietary route.     

Trace element concentrations in Coastal Hawaiian waters

The objective of this work is to characterize the concentrations of selected trace elements (V, Mn, Ni, Fe, Co, Cu, Zn, Se, As, Mo, Cd, Pb, U) in diverse nearshore (50 m), coastal (1.5 km) and seawater well environments within the Hawaiian Archipelago using robust analytical methods that are appropriate for metals analyses in seawater. The sampling sites include locations having varying type, quality and quantity of freshwater input. In most coastal and nearshore cases, the trace element concentrations approximate values characteristic of offshore waters. Concentrations of trace elements in coastal waters that were enriched through either urban or agricultural inputs declined sharply within a short distance from shore; this is taken to indicate the predominant importance of physical mixing/advective processes along with particle scavenging in these dynamic areas. Trace element levels in seawater wells did not evidence any concentration trends consistent with island age suggesting little or no impact of island weathering on metal concentrations; concentration differences among wells appeared to be more dependent on well depth, redox conditions, and/or salinity. Sampling also targeted nearshore locales where ciguatera fish poisoning is prominent because of suggested linkages between trace element concentrations and aberrant dinoflagellate growth. Nearshore stations where ciguatera is prevalent failed to show clearly different trace element levels except for two prominent locales which showed elevated Mn and Fe concentrations.     

Techniques for determination of trace metals in small samples of size-fractionated particulate matter: phytoplankton metals off central California

The oceanic biogeochemical cycles of many trace elements are dominated by their association with the growth, death, consumption and sinking of phytoplankton. The trace element content of marine phytoplankton reflects nutritional status, species composition, surface area to volume ratios, and interactions with bioactive and toxic elements in the ambient seawater. Despite the ecological and environmental importance of trace element assimilation by autotrophs, there are few modern measurements of trace elements in phytoplankton assemblages from the natural environment. Here we introduce a new method for collection and analysis of size-fractionated particulate samples from practical seawater volumes. We pay particular attention to accurate determination of trace element filter blanks which are typically the limiting factor for analysis of such samples. Metals were determined at very low detection limits by high resolution inductively coupled plasma mass spectrometry (HR-ICP-MS) for 11 elements (Ag, Al, Cd, Co, Cr, Cu, Fe, Mn, U, Zn and P, which is used as a biomass normalizer) in three types of polymer filters (0.45, 5.0, and 53 μm pore size) and a quartz fiber filter (0.8 μm pore size). To place these new determinations in a practical context, results are presented for a vertical profile of samples filtered from 1–4 l of coastal seawater (0.3–1.0 mg total solid dry weight) at a station off central California. The results demonstrate that the blanks of the evaluated filter types, precleaned appropriately, are sufficiently low to allow accurate determination of the trace metal content of three size-classes of phytoplankton. At the Pacific station, measured phytoplankton Zn content (as Zn/P) agrees with values predicted from single-species culture studies growing at seawater Zn concentrations expected for coastal waters. The new method has utility as a generally applicable and simple size fractionation technique, and allows determination of natural and pollutant elements in small samples of phytoplankton and particles in coastal, estuarine and offshore marine regimes.     

辽宁省双台子河口潮滩表层沉积物微量元素地球化学特征

对双台子河口潮滩上所采集沉积物样品的微量元素含量进行了测试分析,研究其空间分布特征、元素相关性以及元素组合特征,探索了微量元素在河口潮滩上的迁移富集规律及其控制因素。结果表明:潮滩沉积物中Cu、Pb、Zn元素富集,V元素流失;除Ti、Ba、Sr、Zr外,其余11种元素均表现为高潮滩比中低潮滩含量高;R型因子分析识别出3个微量元素组合,分别是Mn、Rb、Co、Cu等为代表的亲铁亲铜的元素组合,Sr、Ba等与含钾矿物有关的元素组合和Nb、Y等与细粒黏土有关的元素组合。     

海水中微量元素的活性炭吸附预浓集和中子活化分析

应用高分辨率的Ge(Li)γ谱仪,可以对天然水中的多种微量元素进行不破坏样品的中子活化分析,但要得到高的灵敏度,必须在活化前将水中待测元素预先浓集。冷冻干燥预浓集方法成功地用于各种天然淡水,而海水在冷冻干燥后会得到大量的混合盐(主要是NaCl),经过中子活化将产生很强的~(24)Na放射性,干扰其它元素的测定。因此,对于海水多数采用离子交換树脂吸附,溶剂萃取和活性炭吸附等预浓集方法。活性炭的优点是,对水中多种微量元素吸附能力很强,对Na,Cl和     

Trace element bioaccumulation in reef fish from New Caledonia: Influence of trophic groups and risk assessment for consumers

Fourteen trace elements (Ag, As, Cd, Co, Cr, Cu, Fe, Hg, Mn, Ni, Pb, Se, V, and Zn) were analyzed in livers and muscles from 22 fish species from the New Caledonia lagoon, which is subjected to important chemical inputs due to intense land-based mining activities (New Caledonia is the third largest world producer of Ni). The results of this baseline research indicated that livers generally concentrated trace elements to a greater extent than muscles. Nevertheless, the overall trace element concentrations in both tissues were barely above the levels reported in fish and thus contamination at the local scale was poorly discriminated. Although these levels were low, preliminary risk assessment from a global health standpoint suggests that As would be an element potentially leading to exposure of concern for fish consumers. Based on the trace element concentrations in livers and the fish trophic preferences, some trends have been observed among trophic groups: Ag, Cu, Fe, Hg, and Zn concentrations were generally higher in liver of fish with the highest trophic position whereas Cd concentrations were lower in these groups. The use of the leopard coral grouper Plectropomus leopardus as a resident top predator allowed determining the geographical variations in contamination levels with significant differences for six out of the fourteen elements investigated. The sampling sites influenced by anthropogenic inputs were revealed by high Ag, Cd, Cu, Hg, and Pb concentrations. Such geographic differences also applied to Zn but surprisingly not for the typical elements associated with Ni mining, i.e., Co, Cr, Mn and Ni.     

西南印度洋脊49.6°E热液区热液产物和玄武岩地球化学特征

利用X射线荧光法和ICP-MS等方法对取自超慢速扩张的西南印度洋脊(SWIR) 49.6°E热液区的热液产物和玄武岩样品进行元素地球化学特征分析研究,结果表明:(1)与亏损型洋中脊玄武岩(N-MORB)相比,研究区玄武岩样品的主量元素组成显示其偏碱性,而微量元素对比表明该区玄武岩明显富集Pb元素;(2)对热液产物的综合分析表明这些样品多为Fe-Si-Mn氧羟化物且都为热液来源;(3)热液产物的∑REE含量介于玄武岩和海水之间,经球粒陨石标准化的稀土元素(REE)分布模式均表现出Eu正异常和轻稀土(LREE)富集的特征。另外,本研究还表明,利用玄武岩和热液产物地球化学指标不仅能够模拟出以热液喷口为中心的元素地球化学晕,而且能反映出热液活动的影响范围。     

The trace element geochemistry of marine biogenic particulate matter

Plankton samples have been carefully collected from a variety of marine environments for major and trace-chemical analysis. The samples were collected and handled under the rigorous conditions necessary to prevent contamination of the trace elements. Immediately after collection, the samples were subjected to a series of physical and chemical leaching-decomposition experiments designed to identify the major and trace element composition of the biogenic particulate matter. Emphasis was placed on the determination of the trace element/major element ratios in the various biogenic phases important in biogeochemical cycling.The majority of the trace elements in the samples were directly associated with the non-skeletal organic phases of the plankton. These associations include a very labile fraction which was rapidly released into seawater immediately after collection and a more refractory component which involved specific metal-organic binding. Calcium carbonate and opal were not significant carriers for any of the trace elements studied. A refractory phase containing aluminum and iron in terrigenous ratios was present in all samples, even from remote pelagic environments. This non-biogenic carrier contributed insignificant amounts to the other trace elements studied.The plankton samples were collected from surface waters with a wide range in the dissolved trace element/nutrient ratios, however, the same elemental ratios in the bulk plankton samples were relatively constant in all these environments. The bulk compositions and the rapid release of the metals and nutrient elements (specifically phosphorus) from the plankton after collection were used to examine the systematics of depletions of the dissolved elements from surface waters. These elemental ratios were combined with known fluxes of the major biogenic materials to estimate the significance of the plankton in the vertical flux of the trace elements. In parallel with the major surface ocean cycles of carbon and nitrogen, significant fractions of the trace elements taken up by primary producers must be rapidly regenerated in order to explain the observed elemental compositions and fluxes.     

海山当地物源和南极底层水对富钴结壳成矿作用的影响——来自海山周围水柱化学分析的证据

为了了解海山富钴结壳中金属元素的来源及其形成环境,对中太平洋某海山周围两个站位(一个位于海山斜坡上部,另一个位于海山外围较远处)进行了海水水柱综合水化学分析,发现两个站位溶解氧、pH及营养盐的分布是一致的,反映了两个站位海水化学环境的相似性,而剖面上金属元素含量却存在很大差异,位于海山斜坡上部站位的金属元素含量明显高于离海山较远的站位,说明海山结壳的主要金属来源于海山当地的水岩反应甚至低温热液活动。尽管存在差异,但在两个不同站位均存在近底层金属元素含量高,这印证了通过势温分布推断的本区存在南极底层水(AABW)影响的判断,说明AABW在本研究区确实存在,并且是维持海山斜坡强氧化环境的主要因素,AABW可能同时起着输运部分成矿元素的作用,但两个站位水柱金属元素含量的差异主要揭示了海山区存在水岩反应或者低温热液等当地物质的输入。     

Using trace elements in skin to discriminate the populations of minke whales in southern hemisphere

Concentrations of 12 trace elements (V, Cr, Mn, Cu, Zn, Se, Rb, Sr, Cd, Cs, Ba, and Hg) were determined in liver and skin tissues of minke whales from various regions within the Antarctic Ocean. Cd concentrations in livers of southern minke whale were apparently higher than those in cetaceans from other regions, while Hg concentrations were lower. There were significant positive correlations between body length and concentrations of Cd and Hg in the liver. The concentrations of all trace elements in the skin were lower than those in other cetaceans reported previously. Significant positive correlations between liver and skin were found for Cr, Mn, Cu, Zn, Rb, Cd, and Cs, implying that the concentrations of these trace elements in the skin reflect those of internal organs. Large interannual variation of the accumulation pattern of trace elements in the skin was observed for the southern minke whales from Area V. There were significant differences in the skin element concentrations among Areas III, IV, and V, especially for males. Also, discriminant analysis between geographically two different groups collected during 1995/1996 austral summer season, based on the concentrations of trace elements in the skin, allowed for a correct classification of 90% of these minke whales. These results suggest that measurement of trace elements in skin samples could provide valuable information on the status of contamination and possible geographic differences in the accumulation levels in southern minke whales.