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1.
利用高精度的电感耦合等离子体质谱仪对2014年1月长江口表层水中溶解铀浓度及其234U/238U比值、2013年3月长江口表层沉积物中各矿物组分的铀含量及其234U/238U比值进行了测定,研究了其空间分布特征和影响因素。结果表明:除了长江径流和海水之外,长江口还有其他的溶解铀来源。水体中过剩铀与悬浮颗粒物浓度呈现显著相关性（r2=0.96）。对长江口表层沉积物进行的序列提取实验进一步表明,水体中悬浮颗粒物或沉积物中可解吸态和碳酸钙结合态铀可以在河口区域释放进入水体,而铁锰氧化物和有机物结合铀比较稳定,不受河口区混合过程的影响。每千克颗粒物或沉积物能够释放约2 μmol颗粒态铀,使其转化为溶解态。然而,铁氢氧化物和细颗粒物的絮凝吸附作用也可使溶解铀同时从河口水体中清除。在低盐度区,铀的清除和添加过程速率相近,使溶解铀呈现暂时的"伪保守"现象:颗粒态释放的铀具有明显低的234U/238U比值,导致水体的234U/238U低于保守混合值。在中高盐度区域,溶解铀呈现明显的富集现象。但是由于水相和颗粒相中的铀交换,可释放颗粒态铀的234U/238U接近溶解铀的234U/238U比值,从而导致水体的234U/238U比值呈现出保守性。长江口颗粒物的铀释放通量为（3.48±0.41）×105 mol/a,约占输入的总颗粒态铀通量（1.80±0.17）×106 mol/a的19.3%。长江口输入东海的溶解铀总通量（河流溶解态铀与河口添加铀之和）为（2.68±0.13）×106 mol/a,约为世界河流入海铀通量的11.7%。 相似文献
2.
东海秋季典型站位沉降颗粒物通量 总被引：6，自引：0，他引：6
2002年9月在东海的长江口、中陆架区和浙江近岸上升流区三个站位放置沉积物捕获器采集沉降颗粒物。在对颗粒有机碳(POC)、颗粒有机氮(PON)和总颗粒碳(PC)元素分析基础上,采用颗粒物通量模型对沉降通量进行了研究。镜检发现细小无机颗粒物和大颗粒聚合体是三个站位沉降颗粒物的主要形式。大颗粒聚合体有住囊类、粪球聚合体、硅藻聚合体和混杂聚合体四种类型。研究结果显示,东海中陆架区和浙江近岸上升流区沉降颗粒物中POC、PON和PC的百分含量均呈现随水深增加明显降低的趋势,但在长江口,这些成分的含量低且上下均匀。长江口观测到的是大风后的一个实例,存在强烈的再悬浮,各水层颗粒物沉降通量平均(±SE)高达(319.02±65.33)g/(m2.d),尽管如此,沉降颗粒物有机态C/N值却很高(18.0±0.9),明显受陆源颗粒物的影响。POC净沉降通量在浙江近岸上升流区为961mg/(m2.d)(水深55m),在东海中陆架区为123mg/(m2.d)(水深88m),可见浙江近岸上升流区是POC向海底转移的重要区域之一,其垂直转移能力明显高于东海中陆架区。在上升流区域和中陆架区,POC的输出比率大约分别为48%—77%和15%—21%。浙江近岸上升流区和东海中陆架区底层颗粒物再悬浮比率分别为66.50%和88.52%。研究显示,浙江近岸上升流区的水体底层颗粒物受底部平流的影响比东海中陆架区相对较强。 相似文献
3.
海洋中悬浮颗粒物质(SPM)的化学特征和沉积通量的研究对于了解全球物质循环和确定海洋吸收、贮存和转移碳能力的生物地球化学过程具有重要的意义。陆架海洋沉积物的再悬浮作为海洋悬浮颗粒物质的一个重要来源已引起本领域专家的重视(詹滨秋等，1993)。Hosika等(1994)在研究东海陆架和沿岸区时,证实在东海存在一个底层涡动层，其悬浮颗粒物质的含量可达总量的30%-40%。Kusakabe等(1994)运用光透射仪(Bean Transmisso Meter)研究涡动层的颗粒物质,以上研究都未能定量地计算再悬浮的比率。本文根据悬浮颗粒物质特征化学成分的垂直通量以及它们在海洋中自身生成的和沉积物再悬浮的悬浮颗粒物质中含量的关系,建立了定量化学模式,并运用现场资料定量计算东海陆架海洋中悬浮物质的再悬浮比率(αγ)。 相似文献
4.
由于化学溶出、物理溶解以及胞外酶等作用,沉积物捕获器中颗粒物在锚系布放期间会发生一定程度的溶解,从而引起沉积物捕获器中碳、氮颗粒物通量的低估。本文对于1987—1988年南海北部中深层沉积物捕获器中碳、氮颗粒物的溶解作用进行了研究。溶解作用对于碳、氮通量估算的影响大致随着深度的增加而减小。总体而言,颗粒有机碳通量低估约3.8%~40.3%,平均值为26.6%。颗粒氮通量低估约4.2%~76.4%,平均值为43.7%。碳、氮颗粒物的溶出量与颗粒物通量大小关系不明显,但是样品储存时间对于碳、氮颗粒物溶解作用的影响较显著,储存时间较长的样品中颗粒物溶出量更大。 相似文献
5.
采用超低本底液闪β计数的方法,测定了春季黄海、东海海水中溶解态、悬浮物、筛绢颗粒物和雨水中天然32P和33P的比活度.结果显示,上层海水各相33P,32P的比活度相当低,其中TDP的32P,33P比活度的浓度最高,悬浮物次之,筛绢颗粒物最低.海水各相中33P与32P活度比值从TDP到悬浮物、筛绢颗粒物逐渐增大,反映出食物链传递过程中磷的年龄逐渐增加.根据稳态模式的估算结果,海水各相中磷的停留时间具有明显的区域变化特征,其中近岸和内陆架溶解磷的停留时间比外陆架短,仅为3~4 d,意味着近岸和内陆架海区低浓度的磷也可能维持高生物生产力的运转.利用稳态模式还估算出浮游植物的碳同化通量为189~814 mg/(m2·d),浮游动物的碳摄食通量为10~161 mg/(m2·d).此外,通过比较雨水32P,33P的输入通量和海水32P,33P积存量,利用质量平衡方法估算出上层海水POC输出通量为102~972 mg/(m2·d). 相似文献
6.
运用时间序列的沉积物捕获器对海岸与陆架海域沉降颗粒物进行采集,估算沉降通量,并运用多学科综合研究手段分析沉降颗粒物的来源、组成、时空变化及控制因素,可以为海岸与陆架沉积动力过程的研究提供新的研究手段。福建罗源湾的实验表明,夏季罗源湾潮下带小潮至中潮期间的沉降通量为133.20~256.18g/(m2·t);由中潮向大潮变化期间单个潮周期的沉降通量明显增大,台风过后的大潮期间的沉降通量为373.99~590.51g/(m2·t);台风显著影响期间的沉降通量为746.34g/(m2·t);粒度分析及水动力观测结果显示,观测期间罗源湾潮下带沉降颗粒物主要来源于海底沉积物的再悬浮。台湾海峡西北部内陆架海域的实验研究表明,该海域近底部悬浮颗粒物沉降通量最大值为13.34g/(m2·d),由小潮向中潮沉降通量逐渐增大,这主要是由于近底部温盐跃层层位上移,近底部垂向混合作用增强,致使底部再悬浮沉积物向上扩散,并最终被沉积物捕获器捕获。沉积物捕获器可以接收到再悬浮沉积物,结合底部边界层过程的观测研究,可以深入认识海底沉积物的侵蚀、沉降及埋藏过程,在研究海岸与陆架区沉积动力学、泥质区沉积记录的形成过程与保存潜力中扮演着十分重要的角色。 相似文献
7.
九龙江河口区稀土元素地球化学特征 总被引：1，自引：0，他引：1
用电感耦合等离子体质谱（ICP-MS）对2007年10月航次采集的九龙江河口区溶解态、悬浮颗粒态、沉积物样品中的稀土元素（REEs）进行了测定,对REEs的地球化学特征进行研究.结果表明,REEs在各相态中的含量范围如下：溶解态的为0.1 ng/dm^3（Eu）～1.96μg/dm^3（Ce）,悬浮颗粒态的为0.28（Tm）～142.83（Ce）mg/kg,沉积物的为0.25（Tm）～99.65（Ce）mg/kg;溶解态、悬浮颗粒态及沉积物中REEs球粒陨石标准化配分曲线均表现为负斜率型,九龙江河口为LREE相对HREE富集型河口.九龙江河口溶解态、悬浮颗粒态、沉积物三相态中REEs含量受流域土壤、地表径流等源区因素影响较大.Ce异常值在各相态中表现为负异常. 相似文献
8.
多环芳烃(polycyclic aromatic hydrocarbons,PAHs)是指广泛存在于环境中由两个以上的苯环以稠环形式相连的有机污染物。目前发现的大部分PAHs具有致癌、致畸和致突变性,可通过食物链进入生态系统,其毒性和持久性严重影响了生态环境和人类的健康。PAHs的疏水亲脂性使它们在水体中的含量较低,大部分被水体中的悬浮颗粒物吸附,并迅速进入沉积物中。沉积物中的PAHs还能通过食物链的逐级传递向水体释放,造成二次污染[1-2]。 相似文献
9.
九龙江口、厦门西海域磷的生物地球化学研究——Ⅱ.表层沉积物中磷形态的分布及在再悬浮过程中的转化 总被引：5，自引：0，他引：5
本文根据１９８７年３月至１９８８年１２月九龙江口、厦门西海域调查资料、讨论表层沉积物中各种形态磷的分布特征以及在沉积与再悬浮过程中磷形态的转化。结果表明表层沉积物磷含量最高值处距悬浮颗粒物最大沉降速率处下游约５ｋｍ，磷在悬浮颗粒物上主要以颗粒态有机磷存在，在表层沉积物中主要以无机结合态磷存在，缺氧的沉积环境中可溶性磷自表层沉和只物上释放以及吸附在悬浮颗粒物上的磷的解吸作用，是该水域溶解态无机磷再生 相似文献
10.
九龙江口、厦门西海域磷的生物地球化学研究——Ⅱ.表层沉积物中磷形态的分布及在再悬浮过程中的转化 总被引：1，自引：0，他引：1
本文根据1987年3月至1988年12月九龙江口、厦门西海域调查资料,讨论表层沉积物中各种形态磷的分布特征以及在沉积与再悬浮过程中磷形态的转化。结果表明表层沉积物磷含量最高值处距悬浮颗粒物最大沉降速率处下游约5km。磷在悬浮颗粒物上主要以颗粒态有机磷存在,在表层沉积物中主要以无机结合态磷存在。缺氧的沉积环境中可溶性磷自表层沉积物上释放以及吸附在悬浮颗粒物上的磷的解吸作用,是该水域溶解态无机磷再生的两个主要来源。潮汐运动对磷的形态变化有影响。 相似文献
11.
Evaluation of atmospheric transport as a nonpoint source of polycyclic aromatic hydrocarbons in marine sediments of the Eastern Mediterranean 总被引：1，自引：0，他引：1
Coastal marine sediment, air and seawater samples were collected at six sampling stations in the Eastern Mediterranean Sea distant from pollutant point sources. All sediment samples were analyzed to determine polycyclic aromatic hydrocarbon (PAH), black carbon (BC) and organic carbon (OC) contents. The PAH contents of gaseous and seawater samples of the study were determined in order to evaluate the role of air–sea exchange as PAH nonpoint source to the marine sediments. The average concentration of the total PAHs (∑PAHs) in the sediments varied from 2.2 to 1056.2 ng g−1 dry weight. The average BC and OC contents varied from 0.3 to 5.6 and from 2.9 to 21.4 mg g−1 dry weight, respectively. ∑PAH concentration in the marine atmosphere varied from 20.0 to 83.2 ng m−3. Air–water exchange flux (FA–W) estimation has indicated air transport as a significant source of PAHs to pristine marine sediments of Eastern Mediterranean. In addition, the significant correlation between the PAHs and the organic and soot carbon content further suggests the importance of atmospheric input of PAHs to the sediments. 相似文献
12.
珠江虎门潮汐水道多环芳烃的分布、组成及来源分析 总被引：6，自引：1，他引：6
采用GF／F玻璃滤膜对珠江虎门潮汐水道水样进行过滤，分离出颗粒相和溶解相多环芳烃：定量分析结果显示，2001年洪、枯季水体中多环芳烃总最分别是786～2098ng／L和11360～34338ng／L，16种优控多环芳烃含量分别为223～614ng／L和6559～20031ng／L。广州前航道多环芳烃的含量高于狮子洋水样的含量：珠江虎门潮汐水道水体中多环芳烃的含量、分布具有明显的季节变化特征，枯季多环芳烃总量高于洪季1个数量级。多环芳烃的组成及其特祉参数分析表明，珠江虎门潮汐水道水体中多环芳烃主要来源于矿物燃料燃烧和汽车排放。 相似文献
13.
In this study, we examined the distribution of polycyclic aromatic hydrocarbons (PAHs) in a contaminated coastal area and the characteristics of the natural organic matter in tandem. We present a detailed study of PAH concentration, distribution, and organic matter characteristics of three core samples from Pensacola Bay, Florida. Solid-state 13C Nuclear Magnetic Resonance (NMR), pyrolysis gas chromatography coupled with mass spectrometry (GC-MS), and tetramethyl ammonium hydroxide (TMAH) thermochemolysis GC-MS were applied to obtain structural details about the sedimentary organic matter. Elemental compositions (carbon and nitrogen) and estimates of black carbon contents are also reported. These coastal sediments were found to contain more PAHs in the upper 15 cm layers than in the bottom 15-25 cm samples. The samples that contained the most PAHs also contained the least amount of aromatic carbon and contained a significant amount of paraffinic carbon. Lignin-derived pyrolysis and TMAH thermochemolysis products were abundant and generally higher in all of the samples in comparison to those reported for modern coastal sediments, indicating a large flux of terrestrial carbon. The black carbon contents were found to range from 4.3% to 6.8%, which are significantly lower than other reports of black carbon in sediments, which represent as much as 65% of the total organic carbon content. The low black carbon content suggests that this type of refractory carbon may not be as responsible for regulating PAH distribution as indicated by other researchers. 相似文献
14.
Hydrophobic organic contaminants (HOCs) may be used as tracers of particle dynamics in aquatic systems. Internal cycling of polychlorinated biphenyls (PCBs) and polycyclic aromatic hydrocarbons (PAHs) were studied in the mesohaline Chesapeake Bay to assess the role of resuspension in maintaining particle and contaminant inventories in the water column, and to compare settling and suspended particle characteristics. Direct measurements of sediment resuspension and settling conducted in conjunction with one of the sediment trap deployments indicate reasonable agreement between measurements of particle flux using the two different methods. Organic carbon and PCB concentrations in settling solids collected in near-surface sediment traps were remarkably lower than concentrations in suspended particles collected by filtration during the trap deployments, but higher PAH concentrations were found in the settling particles. The different behaviors of PAHs and PCBs in the settling particles are due to their different source types and association to different types of particles. Sediment trap collections in near bottom waters were dominated by resuspension. Resuspension fluxes of HOCs measured 2 m above the bay bottom were as high as 2.5 μg/m2 day for total PCBs and 15 μg/m2 day for fluoranthene, and were 25 and 10 times higher than their settling fluxes from surface waters, respectively. HOC concentrations in the near bottom traps varied much less between trap deployments than HOC concentrations in the surface traps, indicating that the chemical composition of the resuspended particles collected in the near bottom traps was more time-averaged by repeated resuspension than the surface particles. 相似文献
15.
This study examined the concentrations of polycyclic aromatic hydrocarbons (PAHs) in surface sediments collected in July 2004 from eight stations in the Zhelin Bay, one of the most important bays for large-scale mariculture in Guangdong Province. Thirteen individual parent PAH compounds were identified using high performance liquid chromatography with UV detection. The overall average concentration of total PAHs was 477.0 ng/g, ranging from 146.1 to 928.8 ng/g. Low molecular mass PAHs with two to three rings (e.g., acenaphthene) were dominant in each sample. The PAH concentration varied among sampling stations, with the highest concentration observed at bay outlets and the lowest found at stations outside the bay. Ratios of low to high molecular mass PAHs and fluoranthene to pyrene were used to determine the origin of PAHs, and results indicated mainly petroleum-derived contamination. Compared with other bays and harbors around the world, the total concentrations of PAHs in surface sediments at the Zhelin Bay are moderate, but this does not exclude the possibility of potential impact on human consumers because some strong carcinogenic PAHs with high molecular mass were found at the station with a nearby caged-fish and oyster farm. Long-term monitoring of PAH contamination in the Zhelin Bay is recommended to reduce the potential toxicological effects on aquatic organisms and humans. 相似文献
16.
珠江虎门潮汐水道水体中多环芳烃的分布及季节变化 总被引：14，自引：0，他引：14
采用GF/F玻璃滤膜对珠江虎门潮汐水道6个表层水样进行过滤分离出多环芳烃的颗粒相和溶解相,并根据美国EPA标准对多环芳烃进行了定量分析.结果显示,洪、枯季水体中16种优先控制多环芳烃总量分别是223～614,6 559～20 031 ng/dm3;洪、枯季多环芳烃总量分别为786～2 098,11 360～34 338 ng/dm3;广州前航道的污染较狮子洋严重.珠江虎门潮汐水道水体中多环芳烃的含量、分布具有明显的季节变化特征,枯季多环芳烃的浓度高于洪季1个数量级以上,且二环多环芳烃的含量占95%以上,主要呈溶解相形式出现;洪季高环多环芳烃的含量明显升高,主要呈颗粒相形式输运. 相似文献
17.
基于2012年7月对东海的调查,剖析了其水体中各形态碳(pCO2、DIC、DOC、POC)的区域分布特征,估算了海-气界面CO2的交换通量(FCO2),探讨了影响其交换的主要因素,在此基础上,结合历史资料初步分析了近十几年来该海域海-气界面CO2交换通量的变化趋势。结果表明,2012年7月长江口邻近海域相对南部陆架区具有较低的DIC浓度,而DOC与POC的浓度相对较高。调查区域表层水pCO2变化范围为96.28~577.7μatm(1atm为101 325Pa),平均值为297.6μatm,低值区出现在长江冲淡水区(30°~33°N,123°~125°E),高值区主要分布在东海陆架的南部区域。表层水pCO2主要受控于长江冲淡水的输入和混合(盐度)、台湾暖流以及生物生产等。调查海域2012年7月海-气FCO2平均为(-6.410±7.486)mmol/(m2·d),表现东海在夏季是大气CO2的汇区,区域碳汇强度由强到弱依次为:长江冲淡水区(CDW)、黄东海混合水区(YEMW)、陆架咸淡水混合区(SMW)、近岸上升流区(CUW)和台湾暖流区(TWCW),东海夏季每日吸收大气CO2(以C计)约(18.3±19.8)kt。结合历史资料分析发现,近十几年来东海夏季碳汇强度有增强趋势,CDW区的海-气界面CO2通量平均年增速为-0.814mmol/(m2·d),即海水吸收大气二氧化碳每年增加约54.6kt,是夏季东海碳汇增加的最主要贡献者。 相似文献
18.
The oil companies operating in the Norwegian sector of the North Sea have conducted field studies since the mid-1990s to monitor produced water discharges to the ocean. These studies have been used to refine monitoring methods, and to develop and validate a dispersion and impact assessment model. This paper summarizes monitoring data from surveys conducted in two major oil and gas production areas, and compares the results to concentrations of polycyclic aromatic hydrocarbons (PAH) in surface waters predicted by the dose-related risk and effect assessment model (DREAM). Blue mussels and semi-permeable membrane devices (SPMDs) were deployed in the Ekofisk and Tampen Regions and analyzed for more than 50 PAH. PAH concentrations in ambient seawater were estimated based on the mussels and SPMD concentrations, and compared to model predictions. Surface water total PAH concentrations ranged from 25 to 350 ng/L within 1 km of the platform discharges and reached background levels of 4-8 ng/L within 5-10 km of the discharge; a 100,000-fold dilution of the PAH in the discharge water. The PAH concentrations in surface water, predicted by three methods, compared well for the Ekofisk Region. The model predicted higher concentrations than the field-based methods for parts of the Tampen Region; particularly the most tidally influenced areas. Tidally-mediated fluctuations in PAH concentrations in surface water must be considered because they affect the estimation of PAH concentrations from mussel and SPMD residue data, and the predictions by the DREAM model. Predictions using mussels, SPMDs, and modeling support and complement each other; all are valuable tools for estimating the fate and impact of chemical contaminants in produced water that are discharged to the ocean. 相似文献
19.
Seven stations were established in the Quanzhou Bay (24.73°-24.96°N, 118.50°-118.70°E) in China on three cruises to determine the concentrations of polycyclic aromatic hydrocarbons (PAHs) and the numbers of PAH-degrading bacteria in surface sediments. Assessing the biodegradation poten- tial of indigenous microorganisms by measuring the respiratory intensity with the addition of PAHs in sediment samples was also one of the aims of this study. The results show that the total PAH concentrations of the sedimen... 相似文献
20.
Sediments from 19 stations in the Gulf of Maine were analyzed for 16 priority polycyclic aromatic hydrocarbon (PAH) compounds in 1983. Thirteen of the compounds were distributed widely with total concentrations ranging from 10–512 ppb (dry wt). These values are an order of magnitude lower than those observed in the coastal zone but higher than those on Georges Bank. PAH concentration was directly related to grain size, total organic carbon (TOC) and distance from source. PAHs appear to be accumulating in Wilkinson and Jordan Basins but not in Georges Basin. Observed PAH distributions support the conclusion that the principal transport mechanism is through the atmosphere with localized augmentation by sediment resuspension and transport from coastal embayments. 相似文献