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1.
对珠江口淇澳岛海岸带3个站位(QA-11,QA-9和QA-14)的沉积物中不同形态的还原硫(酸可挥发性硫,黄铁矿和有机硫)、总有机碳(TOC)和孔隙水中SO42-,甲烷浓度进行了测定,并且利用稳态扩散模型计算其中2个站位(QA-9和QA-14)硫酸盐还原通量[1.74和1.14 mmol/(m2.d)]和甲烷厌氧氧化通量[0.34和0.29 mmol/(m2.d)]。研究结果表明由于潮间带沉积物受到SO42-供给的限制,因此位于潮间带的QA-11站位硫酸盐还原带较浅(约16 cm);在潮下带的QA-9和QA-14站位,随离海岸距离和水深的增加,硫酸盐还原通量呈现减小的趋势,并且硫酸还原逐渐受到可利用活性有机质的限制;甲烷厌氧氧化对硫酸盐还原的贡献表现出增加的趋势,由19.2%增加至25.5%。三个站位沉积物中按不同形态还原硫含量由大到小列出,它们是有机硫(OS)、黄铁矿(DS)、酸可挥发性硫(AVS)。沉积物中AVS的空间分布与硫酸盐还原通量有正相关性。QA-11和QA-14站位的黄铁矿与AVS硫的含量比值大于3,分别为7.9和3.6,表明两个站位的黄铁矿形成可能受硫酸盐还原作用的控制;QA-9站位黄铁矿与AVS硫的含量比值为2.2,暗示AVS向黄铁矿转化受到可利用活性铁的限制。  相似文献   

2.
Since an important fraction of the organic matter produced by salt marshes is decomposed in situ, macro-benthic communities are particularly exposed to the trace metals retained by these systems. Yet, few studies have investigated the macro-benthic communities using the between-root sediment habitat of the salt marsh halophytes (salt-tolerant plants), or the effect of trace metal pollution on its population dynamics. In the present study, samples were collected in vegetated and unvegetated sediment, in three salt marshes in the Tagus estuary, for trace metal concentration determination in the sediment and in the halophytes roots, grain size determination and macro-benthic organism identification. Data analysis revealed that the distribution of macro-benthic organisms is mainly determined by metal contamination, metal type and by the presence/absence of halophytes, not by the halophyte species. Five different associations were identified: resistant organisms were associated with the highest concentrations of lead (sediment); tolerant organisms with zinc, copper (sediment and roots) and lead (roots); cadmium in the sediment with a lack of macro-benthic life; sensitive organisms with low levels of metals except for cadmium in the roots; and macro-benthos typical of intertidal mudflats with unvegetated areas with low metal contamination.  相似文献   

3.
全球范围内有植被定植的海岸带栖息地(红树林、盐沼和海草床)是巨大的沉积物有机碳碳库,同时也是自然生态系统中最密集的碳汇之一,在全球碳循环中发挥着重要作用。针对江苏盐城海岸盐沼湿地沉积物有机碳的研究,区域上的稀疏性和偏向性限制了其作为区域碳汇能力的可靠估计。本研究采用47个100 cm深沉积柱样的现场调查数据,探讨了江苏盐城海岸盐沼湿地沉积物有机碳含量、密度和储量特征。结果表明,0～100 cm深度沉积物有机碳平均含量和平均密度分别为1.68%和23.07 kg/m3,不同盐沼群落沉积物有机碳含量和密度存在一定的差异,其中有机碳平均含量大小排序依次为互花米草>芦苇>盐地碱蓬,有机碳密度排序为芦苇>互花米草>盐地碱蓬。总体而言,3种盐沼群落沉积物有机碳含量的垂向变化趋势与有机碳密度变化趋势具有一致性,芦苇和互花米草表聚性明显。沉积物有机碳含量与其理化性质有关,互花米草群落沉积物有机碳含量具有明显的粒度控制效应,而其他群落不显著。3种盐沼湿地类型0～100 cm深度沉积物总碳储量约为6195.27×103Mg C。研究成果揭...  相似文献   

4.
Community metabolism and nutrient, iron (Fe) and manganese (Mn) cycling were examined in two intertidal, marine, microbial mat communities during short (4–5 days) incubations in closed, flow-through microcosms. Sediment microcosms were incubated under either light (light–dark cycles) or dark (continuous darkness) conditions to assess the effect(s) of photosynthetic oxygen production and microalgal activity on nutrient, Fe and Mn cycling. The effects of chemical redox reactions between reduced sulphur (S), Fe and Mn cycling were examined by blocking sulphate reduction, and reduced S production, with 25 mM molybdate while incubating under dark conditions.In light-incubated microcosms, negligible fluxes of nutrients (nitrogen and phosphorus) and trace metals were observed. A substantial sediment–water flux of reduced Fe (Fe2+) and Mn (Mn2+) was observed in microcosms incubated under continuous darkness; highest fluxes were observed in molybdate-amended microcosms. At both sites, biologically-mediated redox reactions accounted for a substantial (>50%) portion of the Fe2+and Mn2+flux. Both microbial mat communities exhibited similar rates of gross photosynthetic oxygen (O2) production, but dramatically different rates of net benthic O2flux. Distinct patterns of net O2production and trace metal cycling arose from differences in either trace metal oxide availability or reactivity (mineralogy), organic carbon mineralization rates, or sediment characteristics (porosity). Variations in the microbial community responsible for trace metal cycling could have also contributed to the pattern. The present data illustrate that chemically-mediated redox reactions between metal oxides and reduced S complicate interpretation of Fe and Mn fluxes, underscoring the need to separate chemical and biological reactions when attempting to determine the role of biological trace metal reduction in organic carbon oxidation.  相似文献   

5.
对南海北部陆坡柱状沉积物样品总有机碳、总硫含量,以及其中的自生黄铁矿形貌、含量进行分析．结果显示,沉积物中黄铁矿（FeS2）、总有机碳（TOC）、总硫（TS）的质量分数分别为0～0,71％、0．37％～1．18％、0．04％～0．81％;黄铁矿和总有机碳、总硫的含量随深度加深逐渐增大,达到峰值后不断减少,三者的分布趋势基本一致;扫描电镜下观察到黄铁矿主要以莓球状集合体和八面体微晶形貌产出,局部层位亦发现管状、生物内膜状和立方体状黄铁矿晶体．表明该区浅表层环境为缺氧环境,硫化物主要以黄铁矿形式产出,其成因与有机质的厌氧氧化作用有关,而甲烷的厌氧氧化作用也可能促使自生黄铁矿的加速形成．莓球状黄铁矿占主导亦指示一种强还原性的缺氧微环境．黄铁矿富集的缺氧环境与下伏地层中天然气水合物分解释放的甲烷有关,为天然气水合物在该区的勘探提供一定的科荤依据．  相似文献   

6.
In a study of the benthic environment of Belfast Lough the structure of the subtidal sediment was examined along with its content of organic matter and selected metals (Cr, Mn, Ni, Cu, Zn, Pb). A wide range of sediment types occurred within the lough but the mean grain sizes for individual sites lay predominantly within the size classes of fine sand, very fine sand and silt. The content of organic matter and metals in the sediments showed strong positive correlations with each other and with the content of silt/clay. Both organic matter and metals decreased in concentration in a seawards direction. The content of organic matter lay generally within the range of 1–5% which is normally associated with shelf sediments, but constituted up to 12% of the sediment in the docks area. Likewise, metals were usually within the range reported within other nearshore coastal waters of the U.K., but sediments in the docks area and inner lough were enriched with several metals. Cluster analysis identified four major subdivisions in the lough which were distinctly different in their contents of silt/clay, organic matter and metals.  相似文献   

7.
Profiles of trace contaminant concentrations in sediment columns can be a natural archive from which pollutant inputs into coastal areas can be reconstructed. Reconstruction of historical inputs of anthropogenic chemicals is important for improving management strategies and evaluating the success of recent pollution controls measures. Here we report a reconstruction of historical contamination into three coastal sites along the US Gulf Coast: Mississippi River Delta, Galveston Bay and Tampa Bay. Within the watersheds of these areas are extensive agricultural lands as well as more than 50% of the chemical and refinery capacity of the USA. Despite this pollution potential, relatively low concentrations of trace metals and trace organic contaminants were found in one core from each of the three sites. Concentrations and fluxes of most trace metals found in surface sediments at these three sites, when normalized to Al, are typical for uncontaminated Gulf Coast sediments. Hydrophobic trace organic contaminants that are anthropogenic (polycyclic aromatic hydrocarbons, DDTs, and polychlorinated biphenyls) are found in sediments from all locations. The presence in surface sediments from the Mississippi River Delta of low level trace contaminants such as DDTs, which were banned in the early 1970's, indicate that they are still washed out from cultivated soils. It appears that the DDTs profile in that sediment core was produced by a combination of erosion processes of riverine and other sedimentary deposits during floods. Most of the pollutant profiles indicate that present-day conditions have improved from the more contaminated conditions in the 1950-1970's, before the advent of the Clean Water Act.  相似文献   

8.
Partitioning of copper, zinc, iron and manganese into oxide, sulfide, organic and silicate fractions has been determined with a selective chemical leaching technique on sediment samples from a core collected in Osaka Bay. The samples have been dated by the210Pb method. Most of the copper and zinc in the polluted surface sediment layer are contained in both oxide and sulfide fractions. This suggests that the transformation of oxides and hydroxides to sulfides under anoxic conditions within the sediment is significant for the fixation of copper and zinc discharged through human activities into the sediment. Manganese is apparently enriched in oxide and hydroxide fractions of the surface layer due to the post-depositional migration of manganese within the sediment. The copper, zinc and manganese contents of the 30 % H2O2 soluble fraction (mostly organic fraction) decrease with depth in the sediment core, and correlate significantly with the organic carbon content. The heavy metal (Cu, Zn, Fe and Mn) contents of the silicate fraction, without exchangeable sites, are almost constant with depth.  相似文献   

9.
测定了湛江湾海域20个站位表层沉积物中的酸可挥发性硫（AVS）、同步浸提重金属（SEM）、TOC含量和Eh值,对AVS、SEM含量的平面分布及AVS与SEM、TOC含量、Eh值的相互关系进行了分析.结果表明：该海域表层沉积物中AVS含量范围为0.004～0.547μmol/g,平均值为0.155μmol/g,SEM含量范围为2.10～4.27μmol/g,平均值为3.32μmol/g,相对其他海域湛江湾海域沉积物表现出AVS含量较低,SEM含量较高的特征.AVS与SEM含量平面分布较一致,湾顶的含量都较高,含量均值分别为0.361和3.52μmol/g,特呈岛以南到湾口呈逐渐减小的明显趋势.调查海域沉积物AVS与TOC含量呈显著正相关,与Eh值呈显著负相关,说明高有机质含量、低氧化还原电位沉积环境有利于AVS的生成.20个站位CSEM5-CAVS的差值均为0〈（CSEM5-CAVS）〈5,说明该海域可能存在重金属的中等毒性生态风险.  相似文献   

10.
Sediment cores from a transect of sealochs, Etive, Sunart, Nevis, Duich, Broom and Torridon in N.W. Scotland were analysed for the trace metals lead, copper, and zinc. In addition, sediment cores from the Clyde Sea Basin (Loch Fyne, the Gareloch, Clyde dumpsite) and from the Irish and Celtic Seas were analysed as possible source areas for contaminated particles. The sediment cores were dated using excess 210Pb and 137Cs, and Al normalisation was used to correct for sediment compositional effects. All cores showed increased concentrations of all trace metals (and M/Al) towards the surface, with a maximum of 280–500% above background being observed in Loch Etive. Only cores from Duich and Torridon (Zn/Al and Pb/Al) and Etive (Zn/Al) did not continue to show an increase in trace metals to the uppermost samples. The burden of atmospherically derived trace metals accumulated over the past 100 years was compared with similar published burdens from a series of freshwater lochs adjacent to the sealochs. Plots of excess 210Pb (used to correct for sediment focusing) against atmospherically derived Pb showed a series of linear relationships of systematically decreasing gradient towards the north-west, away from potential urban sources of lead. It was calculated that 49% (15–77%) of the Pb but only 3% (1–4%) of the Zn and 2% (0–3%) of the Cu reached the sealochs from atmospheric sources. The remaining trace metals deposited in the sealochs came from marine particles. Using trace metal ratios as an indicator of pollutant provenance, it was shown that the trace metals came predominantly from the Irish Sea. There was no evidence of trace metals derived from the Firth of Clyde basin. It was concluded that trace metal contamination from the Clyde and the surrounding industrialised urban area was mainly deposited in the estuary and the Clyde Sea basin with its adjoining sealochs, such as the Gareloch and Loch Fyne.  相似文献   

11.
Vertical distribution (0–15 cm) of the macrobenthic community and its relationships to natural sediment characteristics and trace metal contents and bioavailability were studied at five locations in the lower Douro estuary, Portugal. An analysis of vertical metal distribution, for the interpretation of anthropogenic impact on the estuarine sediments, was also investigated. Sediment characterisation included organic matter, grain size, metals (Al, Fe, Cu, Pb, Cr, Ni, Cd, Zn and Mn), acid volatile sulphide (AVS) and simultaneously extracted metals (SEM). The macrobenthic community had low diversity (14 species), was dominated by small size opportunists and seemed to be controlled mainly by natural factors such as grain size distribution, Al and Fe contents and sediment depth. The vertically heterogeneous distribution of macrobenthic community appears to affect redox status of the sediments and consequently metal bioavailability. Despite anthropogenic contamination in terms of Zn, Cu, Pb, Cr and Ni having already been detected in the north bank, the analysis of vertical distribution was essential for the identification of current anthropogenic contamination in terms of Zn, Pb and Cd in the south bank.  相似文献   

12.
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   

13.
Denitrification influences the nitrogen budget in estuaries by removing fixed nitrogen from the inorganic pool; rates are dependent on both geological and geographic conditions as well as increasing anthropogenic impacts. In this study the effects of copper (Cu), chromium (Cr), zinc (Zn), cadmium (Cd) and lead (Pb), on the denitrification pathway were evaluated in subtidal and intertidal sediments of the Douro River estuary. Dinitrogen, N2O and NO2− production rates were measured in triplicate slurries of field samples under different treatments of metal concentrations. Results demonstrated that similar metal amendments led to different site responses for denitrification, suggesting that variations in sediment properties (metal concentrations, grain size, organic matter content, etc.) and/or differences in denitrifying community tolerance modulate the level of metal toxicity. Denitrifying communities in subtidal muddy sediments were not affected by increasing concentrations of metals. In contrast, intertidal sandy sites revealed high sensitivity to almost all trace metals tested; almost complete inhibition by Cr (95%) and Cu (85%) was observed for 98 and 79 μg per gram of wet sediment respectively, and by Zn (92%) at the highest concentration added (490 μg per gram of wet sediment). Moreover, the addition of trace metals stimulated N2O and NO2− accumulation in intertidal sandy (Zn, Cu, Cr and Cd) and muddy sediments (Cu and Zn), demonstrating a pronounced inhibitory effect on specific steps within the denitrification enzymatic system. In summary, the results obtained suggest that, according to the type of estuarine sediment, trace metals cannot only reduce total N removal from an estuary via denitrification but also can enhance the release of N2O, a powerful greenhouse gas.  相似文献   

14.
胶州湾李村河口沉积物中重金属分布特征及其控制因素   总被引：6，自引：2，他引：6  
对胶州湾李村河口4个站点沉积物中的酸可挥发性硫化物(AVS)以及同步提取金属元素(SEM,包括Cu,Cd,Ni,Pb和Zn)的含量进行测定,以研究重金属元素在河口海湾沉积物中的分布特征及影响其分布的因素。结果表明,J1站表层沉积物中同步提取金属含量高于其它站点;除J1站外其他站点的同步提取金属的总量随沉积物深度变化范围不大;J1站的SEM/AVS比值始终小于1,其他站点SEM/AVS比值只在沉积物浅表层大于1。此外,AVS和同步提取Fe的含量对沉积物中同步提取金属的分布有着重要影响,其他的因素如有机质的含量等也会对沉积物中同步提取金属的分布产生影响。  相似文献   

15.
Suspended sediments from large and middle size Chinese estuaries, including the Yalujiang, Shuangtaizihe, Luanhe, Jiaojiang and Zhujiang, were analysed to understand trace metal transport in the coastal zone. The determinations of 13 major and trace elements plus organic carbon were made of total concentrations and were fully validated by certified reference materials (CRMs). The combination of the data sets with other Chinese estuaries, such as Changjiang and Huanghe, provides an overview of particulate trace metal geochemistry in this region. Trace metal levels in Chinese rivers are relatively low compared with those draining industrialized regions of Europe and North America. In the estuaries, most particulate elements illustrate stable distribution in the mixing zone until a salinity of 30, especially when absolute concentrations are normalized to aluminium, although the total suspended matter (TSM) is quite different in time and space. Using Al as a reference, it was estimated that 25–40% for Cu, and 5–20% for Pb could remain in labile part in the Jiaojiang, Shuangtaizihe and Zhujiang, whereas different features of labile elements were found in the Changjiang and Luanhe. The mean enrichment factor (EFm) increases with higher sewage to river runoff ratio (S/R) over the drainage basin and EFm for suspended matter is higher than that for bottom sediments. Finally, inputs of particulate trace metals to the coast are estimated based on the riverine sediment load and chemical compositions.  相似文献   

16.
Forty four core samples were analyzed to determine sediment particle size, total organic carbon (TOC), total inorganic carbon (TIC), total nitrogen and total sulphur. Sequential extraction of S was also carried out, differentiating AVS (acid volatile sulphide), elemental S, organic S and pyrite S. The results obtained show that the presence of mussel rafts causes intense changes in the physicochemical composition and properties of the sea floor in the Ria de Arousa. The percentage of silt and clay, TOC, TIC and total N were significantly higher in the biodeposit than in the sediment. In contrast, there were no differences between the biodeposit and the sediment in terms of pH (8.0-8.7) and redox potential. The sediment and biodeposit were always anoxic, with values of redox potentials below -100 mV. In accordance with these conditions, the dominant fraction of S was pyrite S (FeS(2)). The AVS fraction and elemental S were present at low concentrations, except in the uppermost part of each core. Pyrite was relatively stable when the biodeposit and sediment were maintained in suspension for 8 days in oxic sea water; unlike the AVS fraction, which disappeared within a few hours.  相似文献   

17.
Vertical profiles of total sulfur and organic carbon have been measured in two deep-sea piston cores from the southwestern Japan Sea where sulfate reduction is proceeding within the sediments. The content of total sulfur, most of which is present as pyrite, increases gradually with increasing depth, showing several peaks. The amount of diagenetically deposited sulfide-sulfur is estimated using a steady-state model that considers vertical change in the diffusion coefficient. It is suggested that two-thirds to three-fourths of the observed total sulfur content has been deposited diagenetically.  相似文献   

18.
The resuspension of 65 marine sediments was simulated in the laboratory with elutriates from 30 different sites from the north coast of Spain. The partitioning of Cu, Pb and Zn between sediment and elutriate was studied as a function of different physicochemical characteristics of the sediment: organic matter (OM), fine fraction (FF), redox potential and acid volatile sulfides (AVS). Mean remobilization factors (RF) -calculated as metal concentration in the elutriate (μg/L) divided by metal concentration in the sediment (μg/g dry weight)- were 0.072 for Cu, 0.012 for Pb and 0.071 for Zn. Remobilization of Pb was significantly lower than that of Cu and Zn. Although AVS, OM and FF presented a strong intercorrelation, OM explained great part of the variability on Cu and Pb remobilization while AVS did it for Zn. A multiple regression model considering both OM and AVS explained slightly better the remobilization of Pb and Cu, but not that of Zn.  相似文献   

19.
The early diagenesis of trace elements (V, Cr, Co, Cu, Zn, As, Cd, Ba, U) in anoxic sediments of the Achterwasser, a shallow lagoon in the non-tidal Oder estuary in the Baltic Sea, was investigated in the context of pyrite formation. The dissolved major redox parameters show a two-tier distribution with transient signals in the occasionally re-suspended fluid mud layer (FM) and a permanently established diagenetic sequence in the sediment below. Intense microbial respiration leads to rapid depletion of O2 within the uppermost mm of the FM. The reduction zones of Mn, Fe and sulfate overlap in the FM and in the permanently anoxic sediment section which appears to be a typical feature of estuarine sediments, under low-sulfate conditions. Degrees of pyritization (DOP) range from 50% in the FM to remarkably high values > 90% at 50 cm depth. Pyrite formation at the sediment surface is attributed to the reaction of Fe-monosulfides with intermediate sulfur species via the polysulfide pathway. By contrast, intense pyritization in the permanently anoxic sediment below is attributed to mineral growth via adsorption of aqueous Fe-sulfide complexes onto pyrite crystals which had originally formed in the surface layer.The studied trace elements show differential behavior patterns which are closely coupled to the diagenetic processes described above: (i) Zn, Cu and Cd are liberated from organic matter in the thin oxic layer of the sediment and diffuse both upwards across the sediment/water boundary and downwards to be trapped as monosulfides, (ii) V, Cr, Co and As are released during reductive dissolution of Mn- and Fe-oxyhydroxides, (iii) U removal from pore water occurs concomitantly to Fe reduction in the FM and is attributed to reduction of U(VI) to U(IV), (iv) the Ba distribution is controlled by reductive dissolution of authigenic barite in the sulfate reduction zone coupled with upward diffusion and re-precipitation. The incorporation of trace elements into pyrite is most intense for Co, Mn and As, intermediate for Cu and Cr and little to negligible for U, Zn, Cd, V and Ba. The observed trend is largely in agreement with previous studies and may be explained with differing rates for ligand exchange. Slow and fast ligand exchange and thus precipitation kinetics are also displayed by downcore increasing (Mn, Cr, Co and As) or constantly low (Zn, Cu, Cd) pore water concentrations. The downward increasing degrees of trace metal pyritization (DTMP) for Co, Cu, Zn and As are, in analogy to pyrite growth, assigned to adsorption of sulfide complexes or As oxyanions onto preexisting pyrite minerals.  相似文献   

20.
The contents of Fe, Mn, Cu, Co, Ni, Pb and Zn in the seaiment associated with manganese nodules from the Northern Central Pacific Ocean and in their acid-soluble fractions were determined and correlations among the elements and between the trace metals and environmental parameters were discussed. It has been found that the contents of Mn, Cu and Ni in the sediment are one order of magnitude higher than those in the common sediment. As shown in the manganese nodules, they may mainly derive from seabed. The contents of all trace metals in the sediment are obviously governed by Fe-and Mn-oxides, organic matter, seawater depth, particle size and Eh. Multi-element correlation equations were developed for all trace metals. The trace metals in acid-soluble fraction of the sediment were also much higher than ihose of common sediment and negatively correlated with water depth, implying the possible influence of carbonate speciation.  相似文献   

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