首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到19条相似文献，搜索用时 248 毫秒
1.
本文利用取自浙江椒江河口3个未扰动柱状沉积物样,进行了孔隙水化学测试、固相沉积物的活性分量与黄铁矿分量的分级提取和测试,结果表明：Hg主要以黄铁矿态形式存在于沉积物中。As在有机碳较高的河口区潮上带和沉积速率较慢的潮下带主要以黄铁矿形态存在[DTMP（degree of trace metal pyritization,痕量元素黄铁矿矿化程度）〉50%）],而在中潮带As的黄铁矿矿化程度略低（DTMP均值为40.99%）,研究区DOP（Fe的黄铁矿矿化程度）值普遍较低（〈35%）,Mn-DTMP低于3.32%。从而揭示了浙江椒江河口沉积物在数厘米以下,毒性痕量元素Hg和As被高度黄铁矿矿化的规律性,并指出在遇有海事活动或风暴潮事件对海底沉积物进行扰动时,河口沉积物与充氧的海水反应,高度黄铁矿矿化的痕量元素会转变成活性态,从而导致近海生态系统的毒性事件。  相似文献   

2.
关中娄土剖面中重金属元素的垂直分布规律研究   总被引：8，自引：0，他引：8  
郑国璋 《地球学报》2008,29(1):109-115
通过对关中平原西安污灌区、宝鸡峡灌区、交口灌区关中娄土剖面土壤样品的采集、监测,重点分析了对土壤环境及人体危害较大的Cd、Pb、As、Cr等重金属元素在土壤剖面中的垂直分布和淋失迁移的特征.结果表明:在长期污灌的条件下,关中娄土剖面中的Cd、Pb、As、Cr含量具有在土壤耕作层富集的特征,关中娄土剖面中的Cd、Pb含量具有从耕作层向土壤下层递减的趋势,As、Cr含量从耕作层向土壤下层递减的趋势不明显.关中娄土剖面中的Cd、Pb、As、Cr含量在80～100 cm土壤粘化层中均具有明显增高的趋势,为土壤剖面中重金属元素垂直分布的转折层.关中娄土剖面中重金属元素的淋失率具有CA>Cr>As>Pb的特征,且土壤剖面中重金属的淋失率具有从耕作层、犁底层、老耕层、古耕层、粘化层垂直递增的趋势.当污灌区土层中的重金属含量高时,土壤剖面中的重金属元素Cd、Cr、As、Pb均可向土壤下包气带土层淋虑迁移,对地下水的安全构成威胁.  相似文献   

3.
3个未扰动柱状样分别采自浙江椒江口潮间带高、中、低潮带,用冷盐酸法测定了沉积物中酸可挥发硫化物(AVS)及同步提取金属（SEM）,分析了不同潮位沉积物剖面类型及形成机理,并根据SEM-Me/AVS比值评价痕量金属（Cu、Pb、Zn、Cd、Cr、As、Hg及Ni）的活性和生物有效性。结果表明：在高潮带和低潮带形成了薄活动层剖面（<6 cm）,痕量金属的活性态浓度较低,AVS浓度较高;而中潮带形成了厚活动层(约26 cm),痕量金属的活性态浓度较高。潮间带不同潮位痕量金属活性态浓度剖面类型的形成是沉积速率、有机质供源及所处潮位共同作用的结果。在河口区应该存在表层mm尺度上的高值有机碳（C有机）分布。  相似文献   

4.
在浙江椒江口潮间带采集了3个未扰动沉积物柱状样,并采用分级提取方法获得了沉积物各痕量金属的活性态和黄铁矿态分量,同时采用冷扩散法测试了酸可挥发性硫化物(AVS)。结果表明:研究区痕量金属黄铁矿矿化程度(DOP)较低,痕量金属存在较大的活性,容易参与水生系统的生物地球化学循环;但各元素的痕量金属黄铁矿矿化度(DTMP)存在较大差别,即元素As和Hg的DTMP值最大,Cu、Zn、Cd、Cr和Ni中等,Pb和Mn最小。控制黄铁矿矿化程度的因素包括沉积物是否存在大量的有机碳(OrgC)、AVS以及是否存在隔氧的还原系统。  相似文献   

5.
为探究红树林沉积环境自生黄铁矿形貌特征及其分布规律,利用新西兰北岛红树林沼泽区三个不同植被带采集的沉积物柱状样品,在偏光显微镜及扫描电镜下对其不同深度沉积物样品中黄铁矿数量及形貌特征进行了分类、统计。结果表明:(1)三个植被带沉积物样品中均存在莓球状黄铁矿、团块状黄铁矿、结核状黄铁矿及晶粒状黄铁矿,且结核状黄铁矿占比最高;(2)莓球状黄铁矿平均粒径7.77μm,微晶形态以八面体和五角十二面体型为主;(3)相比光滩区、内部林区两个植被带,红树林林缘区沉积物的莓球状黄铁矿粒径变幅较大,自形晶含量最高。初步判断本研究区沉积环境属于贫氧沉积环境,红树林林缘区水环境动荡,黄铁矿发育程度较高。相比中国海南省、厦门红树林湿地及美国西海岸Elkhorn Slough盐沼湿地沉积环境,本研究区红树林沉积环境更封闭,促进了自形晶的广泛发育。  相似文献   

6.
廖启林  任静华  姜丽 《江苏地质》2018,42(4):651-661
通过对河流沉积物等地表沉积物中重金属元素分布等环境地球化学调查数据的统计分析,总结了江苏典型地区河流沉积物中重金属元素的分布特点与规律:江苏局部地区河流沉积物中,Cd、Pb、Zn、Cr、Cu、Ni、Hg等相对富集趋势明显,Cd最大富集倍数 100;不同河流沉积物的重金属元素分布存在差异,与其污染来源密切相关;工业排放是导致河流重金属污染的主要原因,使用含Cd的颜料作为调色剂导致部分河流出现严重Cd污染;与土壤等其他地表沉积物相比,河流沉积物中重金属元素的分布更不均衡。查明河流沉积物的重金属元素分布可为相关农产品安全性预测、确定重金属污染来源、追踪涉重产业的发展历程、防治局部耕地重金属污染等提供科学依据。  相似文献   

7.
滇西沘江沉积物剖面重金属元素分布特征   总被引：3，自引：0，他引：3  
采用连续提取法测定流经兰坪金顶铅锌矿区的沘江3个沉积物剖面中重金属元素的含量,分析Pb、Zn、Cd和As在流域的分布特征和在沉积物剖面中的分布特征。结果表明,距矿山75km的河段沉积物中,浅层沉积物中4种金属元素均污染严重,金顶铅锌矿是沉积物中重金属元素的主要来源,随着矿山开发规模的不断扩大,污染程度加深。4种重金属元素中Cd活性态比例高,且污染程度最强、范围最广、深度最大,Zn、Pb次之,As污染相对较轻、范围较小。潜在生态危害指数法研究结果表明,浅层沉积物中重金属元素表现出中等—很强的生态风险性,产生生态危害的主要重金属元素是Cd,其后依次是Pb、As和Zn。  相似文献   

8.
选取珠江三角洲冲积平原区4个不同沉积相带的第四系岩心做元素全量分析,并对4种重金属进行了赋存形态分数分析,揭示了珠江三角洲第四系元素地球化学特征主要受物源和沉积环境的控制。不同沉积环境下物源的影响程度不同,物源在三角洲平原相的沉积环境下影响强度最大,在海陆交互强烈的沉积环境下,物源的影响减弱,海陆交互作用的影响增强。不同重金属元素由于自身化学性质的差异,其对沉积环境的敏感程度有所不同。研究区Cd富集显著,且其活性态比例最高、潜在生态风险最大;而As,Hg和Pb的富集程度较弱,且As和Hg主要以残渣态的形式存在,Pb主要以残渣态和铁锰氧化物态为主,它们的生态风险相对较低。不同的沉积环境下p H等理化指标对Cd形态的影响不同,Cd的活动态主要与p H和淋滤系数有关。  相似文献   

9.
滇东北矿集区昭通铅锌矿区蚀变岩分带及元素迁移特征   总被引：1，自引：0，他引：1  
围岩蚀变是昭通铅锌矿床的重要找矿标志。通过对矿区760中段98勘探线剖面实测、蚀变岩分带研究、岩石地球化学迁移特征与参数计算,指出围岩蚀变与成矿的关系：热液蚀变分带明显,在蚀变中心,黄铁矿化最强,方解石化、白云石化次之,硅化较弱,黄铁矿化与矿化关系密切;远离矿体,黄铁矿化逐渐减弱,而方解石化、白云石化逐渐增强。强黄铁矿化和强黄铁矿化-强方解石化-强硅化粗晶白云岩蚀变组合是重要的找矿标志。从细晶白云岩带到强黄铁矿化带,元素整体呈迁入形式,主要为与Zn-Pb成矿作用有关的元素,如Ge、Ag、Cd等迁入;同时伴随成矿流体作用,亲铁元素及铁明显富集,显示不同蚀变岩相受热液改造作用影响。蚀变指数（IA）的大小,与矿化强弱呈正相关关系,IA大,则矿化强。  相似文献   

10.
为了认识青藏高原南部雪冰中痕量元素的组成特征、背景含量水平以及人为污染的可能影响,利用高分辨电感耦合等离子体质谱仪首次对2009年4月19日采自枪勇冰川一个40 cm 雪坑中 Al、 Fe、 Ba、 Cd、Co、Cr、Cu、Li、Ni、Zn、Pb、Sb、Sr、U 和 V 共15个痕量元素的浓度进行了测试和研究.分析表明,不同痕量元素之间浓度变化很大,从 Cd 的0.004 ng/g 变化到 Fe 的8628 ng/g;同一痕量元素的浓度变化范围也较大,最大值/最小值从13(Cd)变化到94(Sr).研究表明,不同痕量元素记录反映了人类活动与自然活动的不同影响.对痕量元素地壳富集系数分析表明,岩石和土壤粉尘是 Ba、Fe、Sr、Co、Cr、V 和 U 的主要来源;而人为污染是枪勇冰川中 Pb、Zn、Cu、Li、Ni、Cd 和 Sb 的一个重要来源.对比研究表明,无论是以粉尘源为主要来源的痕量元素,还是以人为源为主要来源的痕量元素,它们的浓度明显高于中亚有关地区冰川中痕量元素的浓度,更远远地高于格陵兰和南极雪冰中的相应浓度,揭示了该地区大气中痕量元素受到粉尘和人为源污染物带来的显著影响  相似文献   

11.
The present study investigates the levels of Mn, Zn, Ni, and Co pyritization in mangrove sediments along distinct sedimentary zones in Enseada das Gra?as, a lagoon-type estuary located on the southeastern coast of Brazil. The coastal geology is characterized by intense interactions of trace metals, forming pyrite minerals. Specific orders of DOP (degree of pyritization) and DTMP (degree of trace-metal pyritization) are shown: supratidal flat?<?mangrove forest?<?mud flat. Distinct changes in content along the sediment profiles are noted, where a supratidal flat presented low levels of DOP and DTMP with little variance along the sedimentary depths. The mangrove forest showed relatively high values of DOP and DTMP in the lower depths, while the mud flat showed the highest levels of DOP and DTMP.  相似文献   

12.
The Gulf of Mannar along the Tuticorin coast is a coral base of the southeast coast of India. To obtain a preliminary view of its environmental conditions, geochemical distribution of major elements (Si, Al, Fe, Ca, Mg, Na, K, P), trace elements (Mn, Cr, Cu, Ni, Co, Pb, Zn, Cd) and acid leachable elements (Fe, Mn, Cr, Cu, Ni, Co, Pb, Zn, Cd) were analyzed in surface sediment samples from two seasons. Geochemical fractionation confirmed the lithogenic origin of metals, which were mainly associated with the detrital phase. The sediments in the gulf are sandy with abundant calcareous debris, which controls the distribution of total and acid leachable elements. Enrichment factors relative to crust vary by a magnitude of two to three and the presence of trace metals indicates the input of Cr, Pb, Cd, Cu and Zn in both forms through industrial activities. Factor analysis supports the above observation with higher loadings on acid leachable elements and its association with CaCO3. The increase in concentration of trace metals (Cr, Pb, Cd, Cu, Co, Ni, Zn) along the Gulf of Mannar indicates that the area has been contaminated by the input from riverine sources and the industries nearby. The present study indicates that other sources should be evaluated in the long-term monitoring program.  相似文献   

13.
《Applied Geochemistry》2003,18(8):1149-1163
A core collected in the Guaymas Basin contained an organic-poor, Mn oxide-rich and (relatively) Fe oxide-rich turbidite layer that affected the distribution of Fe, Mn, C, S and trace metals. Results indicate that sediments not influenced by the turbidite layer achieved a 100% degree of pyritization and, by extension, that pyrite production is Fe-limited in these sediments. In contrast, the mud slide layer apparently supplied enough reactive Fe to transfer essentially 98% of the total S present at the base of the turbidite (17–19 cm) to the pyrite reservoir. C/S ratios showed rapid decreases with depth, from a high of 38 close to the sediment-water interface, to minimum values of 2.8 at the lower limit of the turbidite layer, a ratio equal to the average C/S value of normal marine modern sediments, where concentrations of organic C and pyrite supposedly have attained quasi-steady values. A significant part of the reactive Mn was associated with carbonates (41±12%) and, to a much lower degree, with pyrite (2.7±1.2%). The turbidite layer is currently showing a depletion of Mn relative to the host sediment. It is possible that Mn, a major metal constituent in these sediments, was initially present in high concentrations in the mud slide, but was eventually mobilized and transferred either to the water column or to the sediments immediately below the turbidite layer. Metals associated with this element probably followed the same path, affecting their incorporation into pyrite. The turbidite layer apparently affected the distribution of most of the trace metals associated with pyrite, except maybe Cd, Pb and, to a certain, extent Cr. However, Cu, Cr, Zn, Ni and Co were all found to be highly pyritized (>80%) in the sediments of the Guaymas Basin.  相似文献   

14.
Authigenic pyrite grains from a section of the Lower Toarcian Posidonia Shale were analysed for their trace‐element contents and sulphur‐isotope compositions. The resulting data are used to evaluate the relationship between depositional conditions and pyrite trace‐element composition. By using factor analysis, trace‐elements in pyrite may be assigned to four groups: (i) heavy metals (including Cu, Ni, Co, Pb, Bi and Tl); (ii) oxyanionic elements (As, Mo and Sb); (iii) elements partitioned in sub‐microscopic sphalerite inclusions (Zn and Cd); and (iv) elements related to organic or silicate impurities (Ga and V). Results indicate that trace‐element contents in pyrite depend on the site and mechanism of pyrite formation, with characteristic features being observed for diagenetic and syngenetic pyrites. Diagenetic pyrite formed within anoxic sediments generally has a high heavy metals content, and the degree of pyritization of these elements increases with increasing oxygen deficiency, similar to the degree of pyritization of reactive Fe. The highest gradient in the increase of the degree of trace element pyritization with bottom‐water oxygenation was found for the elements Ni < Cu < Mo = As < Tl. In contrast, syngenetic pyrite formed within a euxinic water column typically is enriched in As, Mo and Sb, but is low in heavy metals, and the geochemical variation reflects changes in sea water composition.  相似文献   

15.
《Applied Geochemistry》1998,13(2):213-233
Porewater concentration profiles were determined for Fe, trace elements (As, Cd, Co, Cu, Mn, Ni, Pb, Zn), sulfide, SO4 and pH in two Canadian Shield lakes (Chevreuil and Clearwater). Profiles of pyrite, sedimentary trace elements associated with pyrite and AVS were also obtained at the same sites. Thermodynamic calculations are used, for the anoxic porewaters where sulfide was measured, to characterize diagenetic processes involving sulfide and trace elements and to illustrate the importance of sulfide, and possibly polysulfides and thiols, in binding trace elements. The ion activity products (IAP) of Fe sulfide agree with the solubility products (Ks) of greigite or mackinawite. For Co, Ni and Zn, IAP values are close to the KS values of their sulfide precipitates; for Cu and Pb, IAP/Ks indicate large oversaturations, which can be explained by the presence of other ligands (not measured) such as polysulfides (Cu) and thiols (Pb). Cobalt, Cu, Ni and Zn porewater profiles generally display a decrease in concentration with increasing ΣH2S, as expected for transition metals, whereas Cd, Pb and Zn show an increase (mobilisation). The results suggest that removal of trace elements from anoxic porewaters occurs by coprecipitation (As and Mn) with FeS(s) and/or adsorption (As and Mn) on FeS(s), and by formation of discrete solid sulfides (Cd, Cu, Ni, Pb, Zn and Co). Reactive Fe is extensively sulfidized (51–65%) in both lakes, mostly as pyrite, but also as AVS. Similarities between As, Co, Cu and Ni to Fe ratios in pyrite and their corresponding mean diffusive flux ratios suggest that pyrite is an important sink at depth for these trace elements. High molar ratios of trace elements to Fe in pyrite from Clearwater Lake correspond chronologically to the onset of smelting activities. AVS can be an important reservoir of reactive As, Cd and Ni and, to a lesser extent, of Co, Cu and Pb. Overall, the trace elements most extensively sulfidized were Ni, Cd and As (maximum of 100%, 81% and 49% of the reactive fraction, respectively), whereas Co, Cu, Mn, Pb and Zn were only moderately sulfidized (11–16%).  相似文献   

16.
The Pimpama River floodplain has developed over the last several thousand years as a result of sea-level fluctuations that shaped the lower catchment and enabled the formation of sedimentary pyrite. The subsequent production of sulfuric acid due to the oxidation of this pyrite enhances the breakdown of metal-bearing sediments and can lead to leaching of major and trace metals into the waters of the region. The seasonal pattern of rainfall and current land-use activities are important aspects that intensify the natural production of acid and influence the release and distribution of metals. To identify the source and migration of metals in the Pimpama catchment and to understand the impact of pyrite oxidation on the distribution of metals in sediments and waters, several components of the drainage system were analyzed: bedrock, sediments from river bed and bank, and water. The elements analyzed in this study (V, Cr, Co, Ni, Cu, Zn and Pb) are all present in the bedrock material which explains their occurrence in the unconsolidated sediments of the floodplain. These metals concentrate in the upper section of the sedimentary sequence and their presence is related to clay minerals such as smectite, organic matter and iron phases. However, Zn, Mo and Co occur in higher amounts than the local background and within standard shale. This comparison suggests that the diagenetic processes alone cannot explain the higher concentrations and it is concluded that these metals also have an anthropogenic source. The formation of sulfuric acid creates conditions for higher mobility of some metals, such as Cr, Co, Ni, Cu, Zn, but does not affect less mobile ones such as Mo and Pb. Over the longterm, the production of acid influences the breakdown of mineral phases and enhances the process of weathering. Over the short term, every rain event leaches acid from sediments and mobilizes metals resulting in a substantial reduction in the quality of river water. Received: 2 October 1998 · Accepted: 16 February 1999  相似文献   

17.
A halocline developed in the GotlandDeep, Baltic Sea, at c. 8.0 14C ky BP, as theresult of a transition from fresh to brackish water.The sediment-water interface changed from oxic topredominantly anoxic, depositional conditions wereperiodically euxinic and pyrite formation wasextensive. This environmental change led topyritization of the upper part of earlier depositedsediments. This study discusses how the distributionof trace elements (As, Ba, Cd, Cu, Co, Mo, Mn, Ni, Pb,U, Zn and V) were affected by the changing redoxconditions, productivity and salinity. The reducingconditions led to pyritization of Cu, Co, Ni, Cd, Mo,Mn and As. Lead and Zn concentrations are very low inpyrite, in agreement with their coordination tosulfide being tetrahedral. Certain elements areenriched in those sediments deposited under euxinicconditions. This enrichment was caused by scavengingof elements dissolved in the water column and isrestricted to elements that have a comparably longresidence time in the Baltic Sea. Molybdenum appearsto be the most unambigious proxy for euxinicconditions, whereas enrichment of U also requiresbrackish water in the productive zone. In the brackishenvironment, enrichment of Ba and V are linked to thecycling of organic carbon. Manganese and As are theonly elements that have been significantly remobiliseddue to the downward moving pyritization front.  相似文献   

18.
利用电感耦合等离子体质谱仪测定了中国南极科考21~27航次期间获取的普里兹湾表层沉积物中Cu、Pb、Zn、Cd、Cr、Co、Al、Fe、Mn的含量,分析了普里兹湾微量元素的分布特征,结合沉积物粒度分布、生物硅含量,并利用富集系数和主成分分析的方法,探讨了微量元素的物源指示意义。研究结果表明:普里兹湾沉积物中的微量元素含量与南大洋其他海域具有很好的可比性。Cu、Zn、Cr、Co、Fe、Mn含量在陆坡深海区明显高于冰架边缘区和陆架区;Al、Pb含量在冰架边缘区较高;而Cd含量在陆架区相对较高。人类活动对普里兹湾沉积物中的微量元素没有明显的影响,南极大陆岩石风化产物和海洋生物源性沉降是其主要来源。冰架边缘区及陆架破折处P2-9站位的微量元素主要为岩源性输入。陆架区、陆坡深海区的微量元素Cu、Zn、Cr、Co、Fe、Mn明显受到生源性物质输入的影响。而普里兹湾沉积物中Cd则主要来源于硅藻的吸收利用及硅质软泥的富集。  相似文献   

19.
The seasonal variation in the trace metals’ concentrations (Cd, Co, Cu, Fe, Mn, Ni, Pb, and Zn) were investigated in surface sediments of the Pandoh Lake. The horizontal distribution of TC, TN, and TP reflects spatial and temporal differences in sedimentary organic production. The chemical sequential extraction of heavy metals was carried out by seven-step fractionation scheme (Leleyter and Probst in Int J Environ Chem 73:109–128, 1999). The significant concentrations of Ni and Cd were associated with “water soluble (Eua)” fraction in the monsoon and winter, respectively, while “exchangeable (Exch)” and “carbonate-bound (Carb)” fractions for Ni and Cd were abundant in winter and summer. The Cd, Cu, and Pb associated with “Exch” fraction in the summer season support their availability on exchange sites due to oxidized nature of surface sediments. Enrichment of Co, Fe, Mn, and Zn in “AFeO” fraction showed poor bioavailability, while Cd, Cu, and Mn in the monsoon, Co in the winter and summer, and Zn in the winter season showed significant “organically bound (Org)” fraction. The ANOVA was significant for chemical fractions of trace elements except “Carb” fraction of Pb and Zn and “CFeO” fraction of Pb. Factor analysis revealed that the “Eua”, “Exch”, and “Carb” fractions together control the metal enrichment of “MnO”, “AFeO”, and “CFeO” fractions in the summer season.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号