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1.
通过分析长江河口湿地典型植物根际沉积物柱样(0～40 cm)中总汞(THg)、甲基汞(MeHg)及其与粒度、总有机碳(TOC)、还原态硫等环境因子之间的关系,探讨了互花米草(Spartina alterniflora)入侵对沉积物中汞形态特征的影响及主控因子。结果表明:(1)不同植物(互花米草、芦苇(Phragmites communis)、海三棱藨草(Scirpus mariqueter)和水葱(Scirpus tabernaemontani))根际沉积物中THg均值为49.9～100.9 μg/kg,其与粒径小于16 μm颗粒物组分体积百分比及TOC含量之间存在显著正相关关系(r2=0.85,p<0.01;r2=0.58,p<0.01),这意味着沉积物中矿物?有机物复合体细颗粒物的空间分异决定着总汞的空间分异。互花米草入侵促进了细颗粒的沉积,进而间接促进了沉积物中总汞含量的增加。(2)不同植物根际沉积物中MeHg均值为0.3～1.4 μg/kg,MeHg/THg均值为0.4%～1.4%,互花米草、芦苇及海三棱藨草根际沉积物中MeHg含量及MeHg/THg值随深度增加不断减小,但无显著差异,表明了互花米草入侵对沉积物中汞甲基化过程的影响可能有限。Pearson相关分析表明,MeHg/THg与THg、TOC、酸挥发性硫之间不存在显著的正相关关系。硫的K边同步辐射结果进一步表明了硫形态(如有机硫和S2?)变化与MeHg变化关系不大。MeHg/THg值呈表层(0～8 cm)高,底层低的分布规律,表明了表层沉积物中汞的甲基化潜势较大,这可能与表层新鲜有机质(如藻类和植物凋落物)的不断供给及其降解过程密切相关,还需深入研究。  相似文献   

2.
胶州湾中汞的含量及其形态的分布规律   总被引：2，自引：0，他引：2  
1987年5月、9月和1988年1月调查了胶州湾表层海水、浮游植物和表层沉积物中汞含量。溶解无机汞含量的变化范围为0.63—4.4ng/dm~3,溶解总汞含量的变化范围为2.5—40ng/dm~3,浮游植物含量变化范围为1.1—25ng/g(湿重)。测定结果表明,胶州湾中汞含量和分布规律与浮游植物的盛衰和陆地迳流有关。有机汞和COD之间存在着线性关系,溶解无机汞含量随叶绿素a含量增加呈指数下降,表明浮游植物对汞的富集及其在海水中形态的转化起着十分重要的作用。  相似文献   

3.
胶州湾海洋黄色物质的生化成分分析   总被引：1，自引：1，他引：0  
在实验室对胶州湾现场水样进行了处理、分析,获得了黄色物质溶液中六种生化成分在胶州湾的水平分布和测定数据,其中测得胶州湾黄色物质溶液中总脂质含量的平均值为21.03mg/dm3,游离氨基酸为1.75mg/dm3,总糖为1.41mg/dm3,氨基多糖为14.23μg/dm3,而胡萝卜素和酚分别为1.13和0.004μg/dm3.黄色物质在胶州湾海水中约为24.20mg/dm3.计算给出了胶州湾黄色物质中总脂质占86.90%,总糖占5.82%,游离氨基酸占7.22%,氨基多糖占0.06%,而胡萝卜素和酚所占比例甚小,与总脂质、氨基酸和总糖相比,约相差几个数量级.分析认为,胶州湾黄色物质以陆源输入为主,其生化成分分布受河流淡水入海流路和湾内环流等影响而被进一步扩散、输送.  相似文献   

4.
对胶州湾水体、浮游生物、悬浮颗粒物和沉积物中锡的测定、形式、生物累积等进行研究。不同季节(1987年和1988年)的水体、浮游植物和沉积物测定表明:1.水体总还原无机锡和总锡含量分别为4.2～38.8ng/dm~3,65.6～209ng/dm~3;浮游植物总锡含量为22.4～414mg/kg(干重);沉积物总锡含量为0.015～0.98mg/kg(干重),且在胶州湾港口区测得水体总锡的最大值209ng/dm~3。以上结果与目前世界其它海域、河口类似。2.有些区域有机锡含量已达到或超过某些生物的致毒阈值(对双壳类,其TBT≤0.1μg/dm~3)从而引起水质恶化。3.水体总锡含量与悬浮颗粒量密切相关;浮游植物对锡的生物富集因子高达10~5,说明无机或有机颗粒及生物体在水体锡的循环迁移过程中起重要作用。  相似文献   

5.
海口湾海水重金属的行为特征   总被引：11，自引：2，他引：9  
本文对海口湾溶解态铜、铅、锌、镉进行了测定.铜的变化范围为:0.47～1.16μg/dm3,平均值为0.78μg/dm3;铅的变化范围为:0.94～2.36μg/dm3,平均值为1.36μg/dm3;锌的变化范围为:1.28～4.83μg/dm3,平均值为3.14μg/dm3;镉的变化范围为:0.005～0.072μg/dm3,平均值为0.030μg/dm3,Cu、Zn的溶解态含量在龙昆路生活污水排污沟口、秀英工业排污沟口及海甸溪口的测站相对较高,Pb、Cd溶解态含量较低,湾内各站平面分布较为均匀.它们的溶解态含量垂直变化趋势为:Cu、Pb、Zn底层大于表层,而Cd表层大于底层.对Cu、Pb、Zn、Cd的颗粒态含量也进行了测定,指出海口湾海水中的颗粒物对重金属的净化起一定作用.对铜的溶解态中的强络合态和不稳态铜也进行了研究,强络合态占总溶解态的比例均在85%以上,对生物起毒性作用有关的不稳态铜含量很低,均小于5nmol/dm3,表明目前海口湾海水中的重金属铜不会对生物生长产生影响.  相似文献   

6.
一、引言 食用海鱼乃为人类从食物中摄入汞、特别是剧毒甲基汞的重要来源。不管被捕捞的海区是否受汞污染,鱼体内常含有占总汞量80—100％的甲基汞。海洋环境中的甲基汞或来源于工业废水或由自然的甲基化作用所合成。鱼能从海水和食物中积累甲基汞,但本身并不能使无机汞甲基化。甲基汞仅在有严重汞污染历史的日本水俣湾检出过。主要是在已知受汞污染地区的一些沉积物中发现有汞,然而浓度很低。有机汞一般占沉积物中总汞的1％以下,但实际上,常常少于0.1％。有人认为沉积物  相似文献   

7.
研究了台州湾海域海水和表层沉积物中15种多环芳烃(PAHs)的浓度水平,评价了表层沉积物对多环芳烃的富集规律,探讨其可能来源.结果表明,表层沉积物中PAHs的浓度范围为85.4 ～ 167.6 ng/g,平均值为138.62 ng/g,总多环芳烃的最大值是椒江码头.表层沉积物中二环、三环、四环、五环和六环多环芳烃占总多环芳烃的百分含量平均值分别为7.8 %,42.1 %, 33.3 %, 9.6 %和 7.2 %,三环多环芳烃的含量最高;表层沉积物对多环芳烃的富集系数为532.7 ～ 1068.9,平均值为807.5,单组分菲的富集系数最高为122.7,最小的是苯并(a)芘为2.7;台州湾表层沉积物中的多环芳烃主要来源于燃煤污染,部分来源于石油烃类物质的直接污染.  相似文献   

8.
日本真海带对硒的积累和生物转化   总被引：4，自引：0，他引：4  
在海水中添加亚硒酸盐(Na2SeO3)及不同浓度的氮磷营养盐(NaNO3+NaHO2PO4),研究海带对硒的积累,通过分离测定海带富硒前后各生化组分的含硒量来探讨硒的生物转化问题.结果表明天然海带含硒量(鲜重)为0.451~0.596μg/g,海带富硒最佳的Na2SeO3浓度为200mg/dm3,培养56h后的富硒倍率约为50.在天然海带中,硒主要以有机态存在,有机硒占总硒含量的86.22%;在含有200mg/dm3NaO2SeO3的海水中培养56h后测得海带的总硒为24.481μg/g,其中有机硒含量为16.703μg/g,无机硒为4.714μg/g;在添加氮磷营养盐的含硒海水中,海带的富硒能力得到进一步的提高,在适宜的氮磷条件下(150mg/dm3NaNO3和25mg/dm3NaHO2PO4)总硒含量达到33.649μg/g,而无机硒含量基本不变,为4.497μg/g,因此提高部分转化为有机硒,有机硒含量达到24.678μg/g.这说明海带具有通过自身代谢将无机硒转化为有机硒的较强的能力.  相似文献   

9.
通过对东北太平洋海域中国多金属结核开辟区沉积物间隙水中铜、锰、镍等微量元素的详细研究表明,锰主要受沉积环境的影响,其含量的变化范围在0.16～8.61μg/dm3之间;铜和镍则主要与表层海水的初级生产力有关,研究区内间隙水中铜和镍含量的变化范围分别为0.16～20.8和0.80～3.12μg/dm3,且这些元素在沉积物—水界面处均存在最大浓度梯度.利用“Fick扩散定律”计算表明,锰在研究区主要是从上覆海水向沉积物扩散,是沉积物中锰的主要来源之一;而铜和镍则是从沉积物向上覆海水扩散,是底层海水中铜和镍的主要来源。与表层海水中铜和镍向底层海水的输送通量计算结果相比,底层海水中铜和镍的含量主要受沉积物的控制.  相似文献   

10.
江锦花 《海洋通报》2007,26(4):85-90
研究了台州湾海域海水和表层沉积物中15种多环芳烃(PAHs) 的浓度水平,评价了表层沉积物对多环芳烃的富集规律,探讨其可能来源.结果表明,表层沉积物中 PAHs 的浓度范围为85.4～167.6 ng / g,平均值为138.62 ng/g,总多环芳烃的最大值是椒江码头.表层沉积物中二环、三环、四环、五环和六环多环芳烃占总多环芳烃的百分含量平均值分别为7.8 %,42.1 %,33.3 %,9.6 % 和 7.2 %,三环多环芳烃的含量最高;表层沉积物对多环芳烃的富集系数为 532.7～1 068.9,平均值为 807.5,单组分菲的富集系数最高为 122.7,最小的是苯并(a) 芘为 2.7;台州湾表层沉积物中的多环芳烃主要来源于燃煤污染,部分来源于石油烃类物质的直接污染.  相似文献   

11.
In Tokyo Bay the concentrations of dissolved gaseous mercury (DGM) in the surface seawater and total gaseous mercury (TGM) over the sea were measured during December 2003, October 2004 and January 2005. Based on these data, the evasional fluxes of mercury from the sea surface were estimated using a gas exchange model. In addition, an automatic wet and dry deposition sampler was used to measure the wet and dry depositional fluxes of mercury from December 2003 to November 2004 at three locations in and near Tokyo Bay. The results indicate that the average DGM and TGM levels of seven locations are 52 ± 26 ng m−3 and 1.9 ± 0.6 ng m−3, respectively, which shows that the surface seawater in Tokyo Bay is supersaturated with gaseous mercury, leading to an average mercury evasional flux of 140 ± 120 ng m−2d−1. On the other hand, the annual average wet and dry depositional fluxes of mercury at three locations were 19 ± 3 μg m−2yr−1 and 20 ± 9 μg m−2yr−1, respectively. These depositional fluxes correspond to the daily average total depositional flux of 110 ± 20 ng m−2d−1. Thus, it is suggested that in Tokyo Bay, the evasional fluxes of mercury are comparable to the depositional fluxes.  相似文献   

12.
汞同位素技术是汞的生物地球化学循环和污染防治研究的重要手段,在汞的源解析和过程示踪等方面具有广泛应用。由于自然环境中汞含量极低,所以环境样品需先经过一系列严苛的预处理才能开展汞同位素分析。目前,用于同位素分析的固态样品前处理方法主要有湿法消解和燃烧捕集法,液态样品的前处理方法以色谱分离、共沉淀和吹扫捕集为主,气态样品则收集至不同的固态吸附剂后,通过燃烧捕集法富集样品中的汞。相比湿法消解,燃烧捕集法具有富集倍数高、干扰元素少、适用范围广、操作简便等优点,广泛应用于土壤、岩石和大气等样品的前处理中。海水样品的前处理以共沉淀的效率最高,而吹扫捕集能富集海水中不同形态的汞。为拓展汞同位素技术在汞的生物地球化学循环研究中的应用,亟需建立更加快捷、高效的前处理技术。  相似文献   

13.
Concentrations of total mercury (THg) and methyl mercury (MeHg) were determined for 32 surface sediments collected along the coastal line of Fujian Province and eastern Guangdong Province. The spatial distributions of THg and MeHg and their environmental impact factors were investigated. The average concentrations of THg and MeHg in the sediments were 31.5 ng/g and 0.096 ng/g, respectively. Both sediment THg and MeHg concentrations showed relatively high value in the Minjiang Estuary and the coastal areas of Quanzhou and Putian. The concentrations overall decreased as the distance to the shoreline increased. The correlations among environmental impact factors and THg, MeHg were analyzed. The sediment THg concentration was highly correlated to the concentrations of organic matter, copper, total nitrogen (TN) and total phosphorus (TP), and significantly correlated to pH value of the bottom seawater and concentration of sediment sulfide. The sediment MeHg concentration was highly correlated to the concentrations of organic matter and copper, and significant correlated to the concentrations of sulfide, TN, TP and pH value of the bottom seawater.  相似文献   

14.
Due to the lack of knowledge regarding annual bioaccumulation rates in estuarine and marine fauna, the main aim of this work was to study the annual mercury bioaccumulation in the well-documented bivalve species Scrobicularia plana along a human induced mercury gradient in the Ria de Aveiro coastal lagoon (Portugal) and in a nearby, non-polluted system (Mondego estuary), parallel to the risks associated with its consumption by humans.Minimum total mercury concentration was as low as 0.019 mg kg−1 (wwt) in 4+ year old organisms in the reference site, where a significant negative correlation (p < 0.05) was found between total mercury concentrations and size, resulting in negative bioaccumulation rates (detoxification). On the other hand, values reached 1.8 mg kg−1 (wwt) in 3+ year old bivalves from the most contaminated area, where a strong positive correlation with size was found (p < 0.01) and annual bioaccumulation rates were as high as 0.25 mg kg−1 yr−1. Annual bioaccumulation rates were highly correlated with suspended particulate matter mercury concentrations. Even though the levels of organic mercury contents increased parallel to the contamination gradient, at each sampling station, no increment was found with age, which corresponded to a decrease in organic mercury percentage with age.In terms of ecological management and public health, the ratio of 0.01 consistently found between Scrobicularia plana annual mercury accumulation rates and SPM mercury levels for most sites may permit to roughly estimate S. plana contamination of commercial sized individuals (>2.5 cm) and, if verified and confirmed in other systems, be used as a simple management tool.  相似文献   

15.
Sediments are the major repository of mercury in estuaries and could be a significant source of Hg to the overlying water column via release from the solid phase during resuspension. There is, however, little information on the effect of resuspension on Hg partitioning and release to the water column. The objective of this study was to determine the effect of resuspension on the cycling of THg and MeHg between the water column and the sediment. Tidal resuspension was simulated using the MEERC STORM facility. The facility can mimic both realistic bottom shear stress and water column turbulence simultaneously. There were three replicates of each resuspension (R) and no resuspension (NR) mesocosms. Two 4-week experiments were conducted in July and October of 2001: experiment 1 without clams and experiment 2 with clams. Both experiments showed that resuspension of muddy sediment introduced significantly higher particulate THg to the water column as TSS increased. The results suggest that THg was mostly bound to sediment particles with very little release during the resuspension events. In contrast, particulate MeHg was significantly lower in the R tanks where sediment particles with poor MeHg were dominant in the water column during the resuspension events. Dissolved THg and MeHg did not change in concert with changes in particulate load, suggesting that the dynamics between dissolved and particulate phases for both THg and MeHg cannot be explained by an equilibrium partitioning.  相似文献   

16.
A series of experiments was conducted to evaluate the appropriateness of cross-flow ultrafiltration (CFUF) techniques for the determination of the phase speciation of monomethyl mercury (MeHg) in natural waters. Spiral-wound cartridge (Amicon S1Y1) and Miniplate (Amicon) were evaluated for their nominal molecular weight cut-offs of 1 and 10 kDa, respectively. The ultrafiltration behavior of standard macromolecules showed that the permeation of high molecular weight (HMW) organic macromolecules was not significant when a concentration factor (CF)>15 was used. The retention of low molecular weight (LMW) molecules was significant, especially at a low CF<5, suggesting that the use of a high CF (15) will minimize the retention of LMW molecules. Sorptive losses of MeHg in the solution phase to the 1 kDa membrane were negligible, but MeHg bound to HMW macromolecules was still retained (20%), even with a preconditioned membrane. The mass balance recovery of MeHg during ultrafiltration averaged 101±15% (n=7) and 105±14% (n=5) for the 1 and 10 kDa membranes, respectively. Sample storage over 24 h caused significant coagulation (47%) of the <10 kDa MeHg into the 10 kDa–0.45 μm colloidal or the particulate MeHg pool. The 1 kDa–0.45 μm colloidal MeHg in Galveston Bay and the Trinity River water samples accounted for 40–48% of the filter-passing MeHg, although the most abundant fraction (52–60%) of MeHg was the truly dissolved fraction (<1 kDa). The partition coefficient between the colloidal (1 kDa–0.45 μm) and truly dissolved MeHg (average log KC=5.2) was higher than the partition coefficient based on particle/filter-passing (average log KD=4.6) or particle/truly dissolved MeHg (average log KP=4.8), suggesting that MeHg has stronger affinity for natural colloids than macroparticulate materials (>0.45 μm).  相似文献   

17.
以胶州湾海泊河口和李村河口为对象,研究了其沉积物中的汞向海水的释放.结果表明,在静态条件下,沉积物汞向海水释放,平衡时海泊河口和李村河口沉积物汞的释放量分别为 0.070 5 ～ 0.117 μg/g 和 0.056 5 ～ 0.093 5 μg/g;汞的释放通量在前 2 h 最大,随后逐渐减小,通量与温度呈指数正相关.通过对汞释放的热力学分析,汞释放的反应热大于零,分别为 9.92 kJ·mol-1 和 9.98 kJ·mol-1,说明汞的释放是一个吸热过程;汞的释放是一个熵增过程;两个实验反应的标准自由能变分别为 2.34 ～ 3.22 kJ·mol-1和 1.19 ～ 2.20 kJ·mol-1,而且温度越高,ΔG0 越小,越利于反应向正方向进行.  相似文献   

18.
The affinity of mercury for organic matter was the most important parameter governing its chemical speciation, transport and toxicity in Controlled Experimental Ecosystems (CEEs) of the Controlled Ecosystem Pollution Experiment (CEPEX) deployed in Saanich Inlet, B.C., Canada, Particulate, colloidal and high molecular weight dissolved forms of mercury accounted for about 90% of the total mercury present in the water column. Bioassays indicated that organic matter in the above size classes had an important influence on the toxicity of mercury to phytoplankton.Sorption of mercury to particulate organic matter in the CEEs could be described by either Freundlich or linear adsorption isotherms. An observed depth-dependent increase in mercury content of particulate matter was attributed to selective biological degradation of non-mercury-binding organic components of the particles during settling.The high affinity of mercury for settling particulate organic matter led to rapid removal of mercury from CEEs. Removal rates could be described as first order and were a function of primary production rates. Deviations of measured half-removal times from those predicted by an empirically formulated relationship between primary production and mercury half-removal times could be related successfully to the influence of other occasionally significant biological parameters such as zooplankton grazing activity.  相似文献   

19.
氮磷营养盐与有机汞联合作用对微氏海链藻生长的影响   总被引：1，自引：1，他引：1  
探讨在高营养盐（氮、磷、硅分别为浮游植物生长的营养盐阚值≥40、50、9倍）条件下，氮浓度及氮磷摩尔比值[n（N）／n（P）]变化、汞（甲基汞和乙基汞）对微氏海链藻（Thalassiosira weissflogii）生长的影响。结果表明，高营养盐区海链藻的生长遵循营养盐限制的唯一因子论；氮浓度和氮磷比提高促进生长，当n（N）／n（P）=64则呈抑制效应；生长初期，甲基汞和乙基汞均产生毒性抑制作用，生长中后期，适量甲基汞（浓度≤1．0μg／L）、乙基汞（浓度≤0．5μg／L）却呈兴奋效应，促进生长；汞形态不同，剂量-效应关系不同。氮和有机汞是海链藻生长的刺激因子。适度有机汞污染与氮富营养化对微氏海链藻的生长产生协同效应。  相似文献   

20.
Understanding the biogeochemical process of Hg is critical in the overall evaluation of the ecological impacts resulting from the reuse of Hg-contaminated dredged sediment. Sediment banks (V1 and V2) were constructed with freshly dredged sediments from a navigational channel in Venice Lagoon, Italy, with the goal of clarifying potential differences in the biogeochemistry of Hg between the reused dredged sediments and those from surrounding sites (SS1 and S2). Toward this purpose, Hg and monomethylmercury (MMHg) concentrations, and Hg methylation rates (MMRs) in the surface 2.5 cm sediments were monitored, along with ammonium, iron, sulfate and sulfide concentrations in the pore waters of banks and surrounding sites from November 2005 to February 2007. Pore water analyses indicate that the bank sediments are characterized by lower levels of sulfate and iron, and by higher levels of ammonium and sulfide compared to the surrounding sediments. With respect to Hg speciation, the fractions of MMHg in total Hg (%MMHg/Hg) and the MMRs were significantly lower in the bank V1 compared to those in the reference site SS1, whereas the %MMHg/Hg and the MMRs were similar between V2 and S2. A negative correlation is found between the logarithm of the particle-water partition coefficient of Hg and the MMR, indicating that the reduced MMRs in V1 are caused by the limited concentrations of dissolved Hg. Organic matter appears to play a key role in the control of MMR via the control of Hg solubility.  相似文献   

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