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1.
微藻矿化去除Pb2+的研究   总被引:1,自引:0,他引:1       下载免费PDF全文
藻类作为水体中的初级生产力,通过生物积累、生物矿化等生理功能与环境中的重金属相互作用、对重金属地球生 物化学循环起到关键作用。为了探讨藻类生物矿化去除水体中重金属的现象,文中研究了淡水微藻FZUL-321对Pb2+的去除 及矿化。结果表明:微藻FZUL-321对Pb2+有较强的去除能力,且是一个快速去除的过程。随着Pb2+浓度增大,该微藻对Pb2+ 的去除效果也增大。在弱酸性条件下(pH5.0),其去除Pb2+的效果较好。如在Pb2+初始浓度为100mg/L,pH5.0,去除时间 为40min,此时Pb2+的去除量为423.2×10-3干重。原子力显微镜(AFM)对细胞表面的形貌进行观察,发现微藻FZUL-321与 Pb2+作用后,细胞形貌和尺寸变化较大,如细胞褶皱并塌陷,细胞表面变得粗糙等。傅里叶红外光谱(FT-IR)结果表明藻 细胞表面的羧基、氨基和磷酸基团等官能团参与前期Pb2+的吸附沉淀。最终,通过一系列生化作用,微藻FZUL-321将离子 态的Pb2+矿化,X射线衍射(XRD)分析显示,矿化产物为Pb5(PO4)3OH。  相似文献   

2.
河南熊耳山地区花山花岗岩与金矿化的关系   总被引:14,自引:0,他引:14  
王长明  邓军  张寿庭 《现代地质》2006,20(2):315-321
熊耳山地区是豫西重要的金矿化集中区。通过对该区花山花岗岩的化学组成、微量元素、稀土元素、稳定同位素特征及与金矿化关系的研究,得出如下主要研究成果:(1)在R型聚类分析谱系图上表明岩体中Au、Ag、Pb、Cu、Ba元素与金矿床微量元素相关性趋于一致;(2)在稀土元素配分模式图上表现出花岗岩和蚀变岩具有相似的右倾配分曲线的特征;(3)在流体包裹体的w(Na+)-w(K+)-w(Ca2++Mg2+)成分三角图上表明金成矿流体和岩浆热液具亲缘关系;(4)岩体线性构造控制了花山地区构造蚀变岩型和爆破角砾岩型金矿床的时空分布;(5)金矿床的成矿时代为燕山期,花山花岗岩的成岩时间集中于81~159 Ma;(6)S、H、O、Pb同位素组成表明成矿物质和成矿流体来自岩浆热液。  相似文献   

3.
为了研究并比较不同微生物在不同钙锶比条件下对钙锶生物矿化过程的调制作用,选取耐辐射奇球菌、酵母菌和大 肠杆菌作为模拟生物矿化的有机基质,通过SEM,FT-IR和XRD对钙锶矿物的形貌、晶型、晶粒尺寸进行表征分析。结果 表明:①当[Ca2+]/[Sr2+]=2时,不加微生物体系中形成的是文石型和柱状方解石型混合晶体,加入微生物组则形成纺锤状方 解石型晶体。此时3种微生物均能诱导锶离子进入碳酸钙晶格;②当[Ca2+]/[Sr2+]=1时,不加菌体系中形成条稀疏的纺锤状文 石型晶体。加入酵母菌和大肠杆菌的体系则形成紧密的纺锤状和簇状文石型晶体,它们能在一定程度上抑制锶离子进入碳 酸钙晶格。而加入耐辐射奇球菌体系形成菜花状方解石型晶体,其仍能诱导锶离子置换钙离子;③当[Ca2+]/[Sr2+]=1/2时,不 加菌体系中形成大小无规则聚集成团的文石型晶体。加3种微生物体系则形成纺锤状或簇状文石型晶体,它们会在一定程 度上抑制锶离子进入碳酸钙晶格。因此,在钙离子浓度较大时,更易形成方解石物相,在锶离子浓度较大时,更易形成文 石物相。  相似文献   

4.
组织坏死后矿(钙)化是甲状腺癌病灶中普遍存在的钙化形式之一,与病变关系密切。利用光学显微镜、环境扫描电镜、高分辨透射电镜及显微红外光谱研究了6例甲状腺乳头状癌中的组织坏死后矿化特征。结果表明,组织坏死后矿化往往发生在胶原纤维丰富的位置,与胶原关系密切。矿化表现出2种形态,矿(钙)化灶内为较为致密的隐晶集合体,其表面及其附近的胶原上沉淀有许多微米级矿化小球,离矿化灶较远的胶原纤维上也散布有矿化小球。一些矿化小球边缘还发育絮状矿化物质,使之形成绒球状外貌。矿化物质结晶程度均较差,由纳米多晶组成。钙化灶中央较致密部分的n(Ca)/n(P)比较高,接近羟基磷灰石的理论比值,而其边缘以及矿化小球的n(Ca)/n(P)比均较低,可能含有磷酸八钙等低n(Ca)/n(P)磷酸钙系列矿物。矿化初期形成纳米多晶组成的微米级矿化小球,矿化小球逐渐聚集形成大面积的矿化灶。  相似文献   

5.
微生物诱导碳酸盐沉淀(MICP)是一种微生物矿化过程,能够胶结松散土体。将其应用于加固土体坡面提高抗降雨侵蚀能力具有潜在的发展前景。通过模拟降雨冲刷试验,对微生物诱导矿化加固前后粉土坡面的径流水动力与侵蚀特性开展研究,分析和讨论了水动力参数之间的相关性以及对土壤剥蚀率的影响规律。结果显示,加固后与加固前相比,粉土坡面径流的弗劳德数平均下降50%;在降雨前期的阻力系数平均下降66%,径流稳定后二者阻力系数接近;径流剪切力平均提高52%。径流系数与坡面入渗速率呈线性负相关(R2=0.857),与加固层的贯入强度呈指数负相关(R2=0.824);入渗速率与加固层的贯入强度呈二次负相关R2=0.930);径流剪切力与坡度呈指数正相关(R2=0.964)。加固粉土坡面的剥蚀率与加固层的贯入强度呈指数负相关(R2=0.822),与径流剪切力线性正相关(R2=0.912),临界径流剪切力为0.5 Pa。对于坡度10~25°的粉土坡面,微生物加固能将其剥蚀率从58.2~118.4 g/m2s降至2.4~21.2 g/m2s,剥蚀率最大降幅可达95.0%。粉土坡面经微生物诱导矿化加固后,水动力参数值发生显著变化,径流特性与水动力参数、加固层特性及坡度相关,坡面的抗冲刷侵蚀性能得到有效提升。  相似文献   

6.
测量了喀斯特地区乌江、沅江两大水系的河流枯水期的主元素、Sr2+离子浓度和Sr同位素比值。这些河流的化学组成代表了流经碳酸盐岩地层的河水的化学组成。这些河流及其支流有高的溶解盐,TZ+变化范围为:2.1~6.3 meq/L,高于全球河流的平均值(TZ+=0.725 meq/L)。河水含有较高的溶质浓度,河水水化学组成以Ca2+和HCO-3为主,其次为Mg2+和SO2-4,Na++K+和Cl-+Si分别只占阳离子和阴离子组成的5%~10%。 这些河流的化学和同位素组成主要受其自流盆地的地质特征控制。流经碳酸盐岩地层的乌江水系河流具有较高的Sr浓度(1.1~9.70 mol/L)和较低的87Sr/86Sr比值(0.7077~0.7110),与流经碎屑岩地层的沅江水系的清水江河流中较高的87Sr/86Sr比值(0.7090~0.7145)及较低的Sr浓度(0.28~1.32 mol/L)形成鲜明的对比。 流域盆地的地理岩性控制了河水的化学组成和同位素组成。对河水的化学计量分析表明河水化学组成受碳酸盐岩溶解控制,而碳酸盐岩主要受碳酸和硫酸作用而溶解。乌江流域受硫酸作用特别明显,表明硫酸主要来源于燃煤或流域盆地硫化物矿物氧化而形成的大气输入。化学元素和同位素比值之间的相互关系表明3个主要来源为:石灰岩、白云岩和硅酸盐岩的风化。同时估计了碳酸盐岩和硅酸盐岩的化学风化速率,结果表明流域盆地的碳酸盐岩风化速率远远高于许多世界大河。岩石风化过程中硫酸的出现或土地的过度使用或土壤植被的退化等都可能是导致流域的碳酸盐岩风化速率如此高的原因。   相似文献   

7.
近年来,在相山铀矿田的西部牛头山地区深部发现了铅锌矿化体,其成因机制不明.为探讨牛头山铅锌矿化体物质来源,开展了硫化物原位硫同位素分析研究.根据硫化物矿物之间的充填和包裹关系判断,铅锌矿化体金属硫化物形成的先后顺序是:黄铁矿形成最早,方铅矿和闪锌矿次之,细脉状黄铜矿形成最晚.利用LA-MC-ICP-MS技术对矿化体中几种金属硫化物分别进行了系统的原位硫同位素分析.结果显示:黄铁矿、闪锌矿、方铅矿、细脉状黄铜矿的δ34S值介于-4.8‰~+5.4‰之间,各硫化物矿物之间硫同位素未达到完全平衡分馏,利用黄铁矿δ34S值得到的矿化流体δ34SΣS值(总硫同位素组成)近似为+3.7‰,与共生矿物对(闪锌矿-方铅矿)图解法得到的闪锌矿和方铅矿沉淀时矿化流体的δ34SΣS值(+3.2‰)相近,表明形成牛头山铅锌矿化体的矿化流体δ34SΣS值大约为+3.7‰,为岩浆硫.结合前人的岩浆岩年龄数据,我们判断该铅锌矿化体金属硫化物的硫可能主要来自次火山岩相花岗斑岩岩浆热液.同一薄片中闪锌矿δ34S值高于共生的方铅矿,表明两者硫同位素基本平衡,利用共生矿物对(闪锌矿-方铅矿)硫同位素温度计计算得出平衡温度为197~476℃,与前人通过脉石矿物流体包裹体得到的铅锌矿化流体温度基本一致.相山火山盆地与相邻的北武夷黄岗山、梨子坑等产铅锌矿的火山盆地具有相似的成矿条件及成矿物质来源,使相山火山盆地具有良好的铅锌多金属找矿前景.   相似文献   

8.
微量元素是岩溶洞穴沉积中非常重要的一类古气候环境替代指标,为近20年来国内外的一个研究热点。总结前人的研究,主要取得了以下一些重要认识:(1)洞穴上覆土壤 和围岩是洞穴次生碳酸盐沉积Mg、Sr的主要来源;(2)Mg/Ca与Sr/Ca能够指示气候环境变化,但需结合其它指标综合考虑。(3)洞穴次生碳酸盐沉积Mg/Ca与Sr/Ca受多种气候环境因素(包括土壤和围岩的组成和性质、水-岩相互作用、先期碳酸盐沉积、分配系数等)影响,其古气候环境指示意义具有多解性;(4)矿物结晶作用对Mg/Ca与Sr/Ca有一定的影响,特别是文石在向方解石转变的过程中容易丢失Mg、Sr,此外,杂质的混入也将抑制Mg、Sr进入方解石,从而引起洞穴次生碳酸盐沉积Mg/Ca与Sr/Ca比值的变化。今后应进一步加强对石笋中这些微量元素的影响机制研究,尤其是对一些影响因素与微量元素含量变化之间的定量关系进行探讨。   相似文献   

9.
沙漠微生物矿化覆膜及其稳定性的现场试验研究   总被引:2,自引:0,他引:2  
李驰  王硕  王燕星  高瑜  斯日古楞 《岩土力学》2019,40(4):1291-1298
将微生物诱导矿化技术应用于原位沙漠覆膜的形成,使得流动沙丘经结皮固定而成为半固定、固定沙丘,从根本上阻断沙尘暴的源头。在内蒙古乌兰布和沙漠腹地选择两个微生物矿化试验区域(TP1和TP3),分别用于两种不同矿化菌种诱导生成碳酸钙覆膜。研究沙漠微生物矿化覆膜的现场试验方法及工艺,对原位矿化覆膜的强度及其在沙漠环境中的长期稳定性进行跟踪检测。采用沙漠土中自行提取的葡萄球菌和传统的巴氏芽孢杆菌两种不同的微生物矿化菌种,通过现场贯入试验检测7、14、28、60、210 d后矿化覆膜沿深度发展的贯入阻力,并将覆膜厚度为2 cm处的平均贯入阻力换算成覆膜层强度,总结覆膜强度随时间的发展变化规律。现场观测结果显示,不同微生物菌种诱导生成的矿化覆膜均在试验的第4天开始形成,到第7天覆膜层具有稳定的强度和厚度,现场检测覆膜的平均厚度为2.0~2.5 cm,经自源葡萄球菌诱导生成的矿化覆膜(TP1)的强度是巴氏芽孢杆菌诱导生成的矿化覆膜(TP3)强度的1.05倍。当经历冬春交替后覆膜层强度都有不同程度的降低,明显地TP3较TP1区域表面剥落更为严重,第210天检测TP3的平均厚度为0.7~1.0 cm,覆膜强度较第7天时降低19%,覆膜内碳酸钙含量较第7天检测时降低15%~30%。而TP1在第210天时的强度较第7天时强度降低仅2%。因此,微生物诱导矿化技术可以应用于沙漠原位覆膜的形成,且沙漠自源葡萄球菌经诱导生成的矿化覆膜层具有更好的强度表现和稳定性。  相似文献   

10.
为了研究不同盐碱程度旱田和水田土壤有机碳(SOC)矿化对氮、磷添加的响应,定量化其激发效应的大小和方向,选择了吉林西部3块盐碱旱田样地(H1,H2,H3)和3块盐碱水田样地(S1,S2,S3),采用实验室模拟培养,将无机营养素((NH42SO4、KNO3和KH2PO4)以7种形式添加到0~15 cm表层土壤样本中,在25 ℃恒温箱内连续监测32 d的CO2释放量,分析7种氮、磷添加处理对SOC矿化和激发效应的影响。结果表明:1)按7种处理形式分别添加200 mg/kg和1 000 mg/kg氮或磷,SOC矿化量和矿化速率均增加了158.5%~876.5%;同一添加物的质量分数越高,SOC矿化量越大,且随着培养时间延长,SOC矿化速率呈逐渐降低的趋势。2)在培养期间,各添加组均产生了正激发效应。3)在培养期间,部分处理组的SOC矿化、激发效应和碱化度表现出显著负相关性(显著性水平p<0.05)。碱化度越大,SOC矿化作用和激发效应越弱;矿化作用越大,正激发效应越低。4)与水田土壤相比,旱田SOC矿化和激发效应对添加氮、磷的响应更大。  相似文献   

11.
西成矿化集中区热水沉积岩物质来源的同位素示踪及其意义   总被引:11,自引:3,他引:11  
利用硅同位素、锶同位素和碳氧同位素,对西成矿化集中区与矿体紧密伴生的热水沉积岩的物质来源进行了探讨。硅质岩的硅同位素δ3 0 SiNBS -2 8=- 0.6‰~ - 0.1‰,硅主要来源于下伏沉积岩;热水沉积岩的锶同位素比值87Sr/ 86Sr变化于 0.70 938~ 0.72 812之间,位于海洋锶和陆壳锶之间,为混合锶,其锶主要来源于下伏沉积地层柱;碳同位素组成略低于正常沉积碳酸盐岩,碳主要来源于下伏沉积地层柱在循环碳,同时又受其它来源碳的影响。同位素研究结果表明,热水沉积岩的组成物质主要来源于下伏沉积地层柱 (地壳内部 ),形成方式主要是外生沉积作用,即热水沉积岩是内生作用与外生作用共同作用的结果,是内外生矛盾的统一体。  相似文献   

12.
近年来,工业和科技的快速发展使得重金属污染土固化/稳定化的修复研究成为热点。运用微生物诱导碳酸钙沉淀(MICP)技术联合吸附材料对锌铅复合重金属污染土进行固化/稳定化的修复,通过无侧限抗压强度试验、毒性浸出试验,评价处理前后污染土的固化效果与重金属的稳定化效果,结合扫描电镜(SEM)和X射线衍射(XRD)等检测手段,揭示MICP技术处理锌铅重金属污染土的修复机制。研究结果表明,采用MICP技术对锌铅重金属污染土进行固化/稳定化之后,可以有效降低污染土中有害重金属的浸出性。当矿化时间为10d时,试样无侧限抗压强度为942.5k Pa;铅的浸出浓度为4.20mg/L,比未处理时降低了44.81%;锌的浸出浓度为4.31mg/L,比未处理时降低了46.19%,效果显著。在此基础上,添加10%的多孔硅吸附材料后,试样无侧限抗压强度可达到1 021 kPa,强度提高了8.3%;铅的浸出浓度为2.45mg/L,与未经处理时相比,降幅达到了67.81%,与单纯MICP方法处理时相比,铅浸出浓度被二次降低了41.67%;锌的浸出浓度仅为2.93 mg/L,与未经处理时相比,降幅达到了63.4%,与单纯...  相似文献   

13.
A small Kuroko-type Cu-Zn deposit exhibiting metal zoning and alteration assemblages comparable with documented proximal volcanogenic deposits, occurs at the top of a felsic fragmental pile, mantling a large sodic rhyolite domal complex. The domal complex occurs within predominantly mafic to intermediate lavas and volcaniclastic rocks with low-potash island-arc tholeiitic affinities, representing the basal section of the early Tertiary (Eocene to middle Miocene) Wainimala Group near the southern coast of Viti Levu, Fiji.Lithogeochemical trends identified in analyses of rock chip samples from traverses across the domal complex reflect alteration zoning. Sodium, Ca and Sr are strongly depleted within the quartz-sericite foot-wall alteration zone (Zone I) 200 m below mineralization. Potassium, Rb and weaker Mn, Zn and Co depletion and Cu, Pb and Mg enrichment define clay-sericite (Zone II) and clay carbonate (Zone III) footwall alteration 600 to 1200 m below mineralization. Hanging-wall albite-chlorite-calcite-zeolite alteration (Zone IV) is accompanied by enhanced Zn, Pb, Co, Mn, Sr and Na values.Significant mine-scale lithogeochemical trends obtained from systematic sampling of a mineralized borehole section include K and Rb enrichment in the zone of strongest quartz-sericite alteration associated with mineralization and broad depletion of Mn, Na, Ca and Sr within altered footwall fragmental rocks. Minor Cu, Pb, Zn and Ag enrichment has accompanied low-grade propylitic alteration of hanging-wall rocks up to 50 m above mineralization. Analysis of weathered bedrock samples from traverses above the mineralized borehole section indicates that primary geochemical trends occur in the weathered zone. Outcropping gossan has strongly anomalous Cu (535 ppm-21.5%), Zn (3300 ppm-6.15%), Pb (420–8200 ppm), As (200–7000 ppm) and Hg (33–670 ppm) values.Application of lithogeochemistry as a follow-up exploration method in a tropical area such as Wainaleka was investigated as a possible replacement for ridge, spur and base-of-slope soil sampling techniques. Ridge-top auger samples and creek outcrop samples were collected at approximately 100 m intervals and a density of 70/km2. Elements (including Cu, Pb, Zn, Mn, Rb, Sr, Na, K, Ca and Mg) were selected for analysis because of specific associations with mineralization and alteration, and low analytical costs. Single- and multi-element dispersions effectively outline mineralization and attendant alteration.  相似文献   

14.
胶东招-掖金矿带金矿化蚀变带Rb-Sr等时线的研究及测定   总被引:1,自引:0,他引:1  
招-掖金矿带已得出三次金矿化的年龄。最早的一次金矿化发生在距今188.94±4.24Ma;第二次金矿化距今100.74±3.58Ma,这两次均属燕山期。最晚的一次金矿化发生在距今46.52±2.290Ma,当属喜山期。几次矿化年龄证明,招-掖金矿带的成矿作用是多次的,每次矿化又是多阶段的,可互相叠加。这充分反映了含矿热液的脉动性。矿体围岩蚀变是金矿化的同步产物,是一个锶均一化的封闭体系。用Rb-Sr等时线法测出其同位素年龄,即为一次金矿化的年龄。几条等时线给出的87Sr/86Sr初始比说明:招-掖金矿带成矿热液来源于大陆壳。  相似文献   

15.
埃达克质岩的金属成矿作用   总被引:12,自引:0,他引:12  
介绍了“埃达克质岩”的术语、与成矿有关的埃达克质岩的分布、成矿背景,讨论了埃达克质岩有利于成矿的控制因素。“埃达克质岩”是指那些具有与俯冲洋壳熔融形成的“埃达克岩”类似地球化学特征,如SiO2≥56%,Al2O3≥15%,亏损Y(≤18×10-6)和重稀土元素(如Yb≤1.9×10-6),高Sr(很少样品的Sr含量低于400×10-6),无-正Eu,Sr异常,贫高场强元素等,但可以形成于不同构造背景并可有不同成因的岩浆岩。埃达克质岩具有重要的金属成矿意义,其有利成矿背景主要包括岛弧、大陆板内伸展和大陆活动碰撞造山带环境。世界上许多(包括三个最大的)斑岩铜矿都与埃达克质斑岩密切共生,因此埃达克质岩的成矿潜力巨大。在岛弧和大陆板内伸展环境中,来自俯冲玄武质洋壳或洋壳沉积物或拆沉的大陆地壳产生的熔体或释放的超临界流体与地幔的相互作用,一方面可能导致熔体被地幔橄榄岩混染,另一方面可能导致高Fe2O3含量的熔体或超临界流体对地幔的交代作用,地幔氧逸度升高,地幔金属硫化物被氧化分解,有利于铜、金等的矿化。  相似文献   

16.
微生物诱导碳酸钙沉淀(microbially induced calcium carbonate precipitation, MICP)是一种在自然界中广泛存在的生物矿化过程。由于MICP具有反应速度快、环境条件要求低、应用范围广、温室气体减排效应显著等特点,在地质、土木、水利、环境多个领域中广泛推广应用。文章在分析国内外相关研究成果的基础上,归纳整理出反硝化过程、硫酸盐还原作用、尿素分解作用等多种微生物诱导下碳酸钙矿化途径和作用机制。以尿素分解菌为代表,重点讨论微生物诱导碳酸盐沉淀过程中pH、温度、离子浓度等环境因素对生成矿物晶型晶貌等方面的影响,总结了MICP的环境应用机制,即环境中的重金属元素通过替换作用替换矿化矿物中的Ca2+或CO32?从而被固定。MICP作为一种简单高效的地质环境过程,在生态环境修复领域具有广阔的应用前景。   相似文献   

17.
Concentrations of trace elements such as As, Ba, Co, Cr, Cu, Ni, Pb, Rb, Sr, V, Y, Zn and Zr were studied in soils to understand metal contamination due to agriculture and geogenic activities in Chinnaeru River Basin, Nalgonda District, India. This area is affected by the geogenic fluoride contamination. The contamination of the soils was assessed on the basis of geoaccumulation index, enrichment factor (EF), contamination factor and degree of contamination. Forty-four soil samples were collected from the agricultural field from the study area from top 10–50 cm layer of soil. Soil samples were analyzed for trace elements using X-ray fluorescence spectrometer. Data revealed that soils in the study area are significantly contaminated, showing high level of toxic elements than normal distribution. The ranges of concentration of Ba (370–1,710 mg/kg), Cr (8.7–543 mg/kg), Cu (7.7–96.6 mg/kg), Ni (5.4–168 mg/kg), Rb (29.6–223 mg/kg), Sr (134–438 mg/kg), Zr (141.2–8,232 mg/kg) and Zn (29–478 mg/kg). The concentration of other elements was similar to the levels in the earth’s crust or pointed to metal depletion in the soil (EF < 1). The high EFs for some trace elements obtained in soil samples show that there is a considerable heavy metal pollution, which could be due to excessive use of fertilizers and pesticides used for agricultural or may be due to natural geogenic processes in the area. Comparative study has been made with other soil-polluted heavy metal areas and its mobility in soil and groundwater has been discussed. A contamination site poses significant environmental hazards for terrestrial and aquatic ecosystems. They are important sources of pollution and may result in ecotoxicological effects on terrestrial, groundwater and aquatic ecosystems.  相似文献   

18.
Carbonate, largely in the form of dolomite, is found throughout the host rocks and ores of the Nchanga mine of the Zambian Copperbelt. Dolomite samples from the hanging wall of the mineralization show low concentrations of rare-earth elements (REE) and roof-shaped, upward convex, shale-normalized REE patterns, with positive Eu*SN anomalies (1.54 and 1.39) and marginally negative Ce anomalies (Ce*SN 0.98,0.93). In contrast, dolomite samples associated with copper and cobalt mineralization show a significant rotation of the REE profile, with HREE enrichment, and La/LuSN ratios <1 (0.06–0.42). These samples also tend to show variable but predominantly negative Eu*SN and positive cerium anomalies and an upwardly concave MREE distribution (Gd-Er). Malachite samples from the Lower Orebody show roof-tile-normalized REE patterns with negative europium anomalies (Eu*SN 0.65–0.80) and negative cerium anomalies (Ce*SN 0.86–0.9). The carbonate 87Sr/86Sr signature correlates with the associated REE values. The uppermost dolomite samples show Neoproterozoic seawater-like 87Sr/86Sr ratios ranging from 0.7111 to 0.7116, whereas carbonate from Cu–Co mineralized samples show relatively low concentrations of strontium and more radiogenic 87Sr/86Sr, ranging between 0.7136–0.7469. The malachite samples show low concentrations of strontium, but give a highly radiogenic 87Sr/86Sr of 0.7735, the most radiogenic 87Sr/86Sr ratio. These new data suggest that the origin and timing of carbonate precipitation at Nchanga is reflected in the REE and Sr isotope chemistry. The upper dolomite samples show a modified, but essentially seawater-like signature, whereas the rotation of the REE profile, the MREE enrichment, the development of a negative Eu*SN anomaly and more radiogenic 87Sr/86Sr suggests the dolomite in the Cu–Co mineralized samples precipitated from basinal brines which had undergone significant fluid–rock interaction. Petrographic, REE, and 87Sr/86Sr data for malachite are consistent with the original sulfide Lower Orebody being subject to a later oxidizing event.  相似文献   

19.
The Tarim basin, which is located in the Xin-jiang Autonomous Region in western China , is alarge-scale superi mposed basin situated between theTianshan Mountains to the north and the KunlunMountains to the south, with an area of 560 000km2. The Tazhong uplift ,locatedin the central partof the basin, has an area of 30 000 km2.It is sur-rounded by the Manjiaer depressionin the north,theTangguzibasi depressionin the south,the Bachu up-lift inthe west andthe Tadong saginthe east .It hasbeco…  相似文献   

20.
Heavy metals are toxic elements that have hazardous effect on the environment. They cause soil pollution as a result of their toxicity, potential reactivity, and mobility in soils. There are so many methods for the measurement of heavy metal concentrations in soils and aquatic systems. The traditional methods used for detecting heavy metal distribution in soil involve laboratory analysis and raster sampling. Both of them are expensive and time-consuming for large areas. Remote sensing techniques are used for obtaining the earth’s surface information, and these techniques have been used in the investigations of heavy metal distributions in preliminary analysis of soils as a rapid method. Today, near-infrared reflectance spectroscopy (NIRS) of soil characteristics has been of interest as a significant object. The present investigation is focused on the detection of heavy metals in contaminated soils by the application of reflectance spectroscopy in the spectral range of 350 to 2500 nm. This study also discusses the circumstances of the applied current methods for the detection and estimation of arsenic (As), cadmium (Cd), nickel (Ni), and lead (Pb) in contaminated agricultural soils. In the first part of laboratory spectroscopy, estimations were done using heavy metal reflectance spectroscopy and partial least square regression (PLSR) approaches, while in the second part, the heavy metal estimations were done using soil organic carbon reflectance spectroscopy through the PLSR approaches. Similar to the tasks above, estimations of As, Cd, Ni, and Pb by using Landsat 8 images were done in the forms of direct and indirect methods and the distribution of heavy metals in the study area was determined. Finally, the results obtained using direct and indirect methods were compared with the wet chemical measurements of heavy metals and organic carbon. It was found that although the direct detection of heavy metals using the images of Landsat 8 produced more accurate results than the indirect detections, the results obtained from laboratory spectroscopy corresponded more with the results from atomic adsorption spectroscopy. On the other hand, based on the fact that the soil has a complex content, the use of nonlinear methods, such as artificial neural networks in predicting soil heavy metal contents, could be regarded as a trusted method.  相似文献   

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