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新疆阿尔泰大东沟铅锌矿床地质特征及稳定同位素地球化学研究 总被引：12，自引：0，他引：12
文章在对大东沟铅锌矿床地质特征进行简要描述的基础上,系统地研究了矿石碳、氢、氧、硫同位素的组成。研究结果表明其形成于火山活动的间歇期,受控于北西向断裂、火山沉积盆地、热液流体及喷流中心。矿体呈层状分布,与地层产状一致,直接容矿围岩为下泥盆统康布铁堡组火山－沉积岩,矿石构造以条带状、浸染状、细脉状为主,矿石矿物成分相对简单,主要为方铅矿、锌矿、黄铁矿等,其中锌的含量高于铅,矿床形成后经历了区域变质作用及热液流体改造。围岩蚀变较发育,矽卡岩化与铅锌矿化关系密切。矿床的34SV-PDB值为-22.3‰～11.7‰,方解石中的13CV-PDB值介于-4.2‰～0.4‰,计算所得的石英及方解石18O水值在-11.4‰～8.4‰之间,成矿流体应该为大气降水与岩浆水的混合物。矿床应属于火山－沉积岩容矿的块状硫化物矿床。 相似文献
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氢氧同位素可以识别水体来源,示踪水循环,自20世纪50年代以来已被广泛应用于水文地球化学领域。已有学者开展了新疆大气降水及部分河流湖泊的稳定同位素研究,而关于阿勒泰地区大气降水之外的地表水体稳定同位素研究尚需加强。本文采用液体水激光同位素分析法开展了新疆阿勒泰地区地表河水、湖泊、山泉水、雪水、锂矿坑裂隙水五类水体的氢氧同位素组成研究。结果表明:阿勒泰地区各种类型水体氢氧同位素组成差异明显,地表河流的δ~(18)O及δD值变化范围分别为-15.4‰～-11.5‰及-114‰～-100‰,氘过量参数(d值)变化范围为-12.4‰～12.4‰;乌伦古湖湖水的δ~(18)O及δD值均远高于地表河流,平均值分别为-5.95‰及-78.5‰,氘过量参数远低于地表河流,均值为-30.9‰。地表河流与全球及乌鲁木齐大气降水线相比差异很大,河水除了大气降水外还受到冰川融水的补给,且在水循环过程中经历了蒸发分馏作用,地表河流之间的氢氧同位素组成差异主要受水体补给来源及蒸发程度强弱的控制。由于氢氧同位素温度效应、纬度效应等的存在,阿勒泰地区水体δD及δ~(18)O与水温(T)、总溶解性固体(TDS)及主要离子Na~+、K~+、Ca~(2+)、Cl~-、SO■摩尔浓度呈显著正相关关系,而与采样点纬度及溶解氧含量(DO)呈显著负相关关系(P0.05,n=32)。本研究获得的氢氧同位素组成特征为阿勒泰地区各类型水体稳定同位素研究提供了基础数据。 相似文献
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氢氧稳定同位素与水-岩相互作用的研究表明,华东相山铀铲田成矿热水溶液的水源属大气降水成因。其δ_(18)O、δD值分别为-6.5—+1.83‰和-60.78—--80.74‰(SMOW),是成矿期大气降水与岩石相互作用的结果,成矿期该区降水氢氧同位素组成的恢复对此提供了佐证。 相似文献
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现代大气降水中的稳定同位素组成是全球或地区性水循环研究的重要载体,同时也是冰芯、湖泊沉积物、石笋等研究领域中,运用稳定同位素来重建古气候的重要依据。本文研究了桂林地区2012年大气降水氢氧同位素组成的逐日变化,根据得到的132组氢氧稳定同位素组成建立了桂林局地大气降水线方程为δD = 8.8δ18O +17.96,大气降水的δ18O波动范围在-13.56‰～+1.07‰,平均为-5.78‰;δD在-101.52‰～+16.02‰,δD平均为-41.03‰。利用降水稳定同位素资料,结合后向轨迹法( Backwards Trajectory) 对桂林水汽来源进行追踪,发现夏季(5-10月)大气降水的水汽来源主要受来自孟加拉湾、南海海洋气团的水汽源的控制,降水的δ18O值偏负,平均为-8.02‰(共64组);冬季(11月至次年4月)大气降水的水汽来源主要受来自西太平洋暖湿气团、冬季风冷气团或西风环流所携带的大陆性气团的影响,不同程度地叠加了局地环流气团、蒸发水汽的补给的影响,降水的δ18O值偏正,平均为-2.86‰(共68组)。研究结果表明,桂林大气降水的稳定同位素组成与降水的水汽来源、季风类型、降水云团来源和性质有关,来自远距离输送夏季风海洋性水汽团形成的降水δ18O值较低(或偏负), 而大陆性气团或局地蒸发水汽循环形成的降水δ18O值较高（或偏正）。不同的水汽来源是决定降水中δ18O值变化的主要因素,因此,通过降水中的δ18O值,特别是其季节变化的特征分析,可以反过来揭示当地降水的水汽来源。 相似文献
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川东北地区酸性气体中CO2成因与TSR作用影响 总被引：3，自引：0，他引：3
通过对川东北地区52个天然气样品化学组分和稳定碳同位素分析,天然气以烃类气体为主,且甲烷占绝对高含量,重烃气体甚微,干燥系数C1/C1+为0.989～1.0。非烃气体H2S和CO2含量变化较大,当二者含量大于5.0％时,具有较好的正相关性。川东北地区天然气中CO2主要包括碳酸盐岩热分解和TSR作用,其中碳酸盐岩热分解生成的CO2含量一般小于5.0％,13CCO2值小于-2‰,且CO2含量与13CCO2值具有正相关性;而TSR作用生成的CO2含量大于5.0％,13CCO2值多大于-2‰,且CO2含量与13CCO2值具有较弱的负相关性。CH4/CO2比值和（H2S+CO2）/（H2S+CO2+∑C1-3）比值能够较好地反映TSR作用程度;当CH4/CO2比值和（H2S+CO2）/（H2S+CO2+∑C1-3）比值分别小于10和大于0.1时,随着TSR作用增强,CH4/CO2比值减少,而（H2S+CO2）/（H2S+CO2+∑C1-3）比值呈指数增加。同时,遭受TSR作用改造的天然气具有较高CO2含量和重的13CCO2,造成13CCO2值与实验结果不一致性的可能原因是在TSR反应过程中部分CO2与硫酸盐中Mg2+、Fe2+和Ca2+等金属离子以碳酸盐的形式沉淀且残余的重碳同位素组成的CO2与酸性气体腐蚀碳酸盐储层形成的CO2相混合。 相似文献
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以云南省蒙自断陷盆地东山山区典型岩溶洼地为研究区,通过野外采集土壤样品与实验室测试分析相结合的方法,运用稳定同位素技术研究旱季不同深度土壤水氢氧同位素组成,揭示区内土壤水氢氧同位素时空变化特征,为进一步研究云南断陷盆地山区土壤水分运移机制和当地农业合理利用和管理水资源提供科学依据。结果表明:(1)土壤水δD、δ18O同位素值的变化范围分别为-128.3‰~-27.6‰和-17.5‰~2.5‰,平均值分别为-96.1‰±20.7‰和-12.3‰±3.7‰,降雨转化为土壤水和水分在土壤中重新分布时发生一定程度的氢氧同位素分馏。(2)旱季两个月份土壤水氢氧同位素组成发生变化,4月份土壤水δD、δ18O同位素平均值分别为-86.3‰±23.83‰和-10.6‰±4.3‰,显著高于2月份(δD:-106.1‰±9.5‰;δ18O:-14.1‰±1.6‰)(p<0.05),主要和4月份土壤水的蒸发作用强烈有关。(3)在空间上,坡地与洼地之间土壤水氢氧同位素组成存在差异,2月份坡地与洼地之间土壤水δD、δ18O值差异显著(p<0.05),洼地土壤水δD、δ18O比坡地偏轻;4月份坡地与洼地之间土壤水δD、δ18O值差异不显著(p>0.05)。(4)土壤垂直剖面方向上土壤水δD、δ18O值随着土壤深度的增加而减小,浅层土壤水δ18O和深层土壤水δ18O存在显著差异,2月份浅层土壤水δ18O比深层土壤水δ18O偏正2.8‰,4月份浅层土壤水δ18O比深层土壤水δ18O偏正10.5‰。 相似文献
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贵州乌江水系枯水期河水硫同位素组成研究 总被引：12，自引：5，他引：12
对枯水期乌江及其主要支流河水的硫同位素组成进行了研究。河水SO42-的δ34S值在-15.7‰～18.9‰之间,干流δ34S值介于-3.7‰～0.0‰之间。主要支流河水的SO42-浓度和δ34S值具有明显的区域性差异:上游碳酸盐岩地区支流河水SO42-浓度较高而δ34S值较低,河水中的SO24-来源于煤中还原态硫的氧化、矿床硫化物氧化和大气降水;下游碳酸盐岩夹碎屑岩地区支流河水则相反,具有较低SO24-浓度和较高δ34S值,河水中的SO24-来源于硫酸盐蒸发岩溶解、大气降水以及煤中还原态硫的氧化。干流的硫同位素组成显示枯水期河水中的硫酸盐主要来源于碳酸盐岩地区。 相似文献
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The concentrations of total suspended sediments (TSS), dissolved organic carbon (DOC) and particulate organic carbon (POC) were measured in water samples taken monthly in the Apure, Caura and Orinoco rivers during a hydrological cycle (between Sept. 2007 and Aug. 2008). The DOC concentration values ranged between 1.5 and 6.8 mgC l−1 in the Apure River; 2.07 and 4.9 mgC l−1 in the Caura River and 1.66 and 5.35 mgC l−1 in the Orinoco River. The mean concentration of DOC was 3.9 mgC l−1 in the Apure River, 3.24 mgC l−1 in the Caura River and 2.92 mgC l−1 in the Orinoco River at Puerto Ordaz. The three rivers showed a similar temporal pattern in the concentrations of DOC, with higher DOC values during the increasing branch of the hydrograph due to wash-out processes of the organic material stored in soils. The mean concentration values of POC were 1.33 mgC l−1; 0.77 mgC l−1 and 0.91 mgC l−1 in the Apure, Caura and Orinoco rivers, respectively. The inverse relationship found between the percentage in weight of the POC and the concentrations of TSS in the three rivers fits a logarithmic model, as it has been previously reported for other worldwide rivers. The POC concentrations in the Orinoco River showed a positive relationship with the TSS, suggesting that the POC in the Orinoco is the result of terrestrially organic matter. Although the fluxes of organic carbon (OC) in the three studied rivers are dependent on the values of water discharge, the fluxes of DOC during the increasing branch of the hydrograph are higher than those found during the decreasing stage, due to the yield of organic material accumulated in soils during the preceding dry season. The mean annual flux of total organic carbon (TOC) of the Orinoco River at Puerto Ordaz was about 4.27 × 106 TonC yr−1. Of this, 3.28 × 106 TonC yr−1 (77%) represents the flux of DOC and about 0.99 TonC yr−1 (23%) represents the flux of POC. The mean annual input of TOC from the Apure River to the Orinoco River was about 4.92 × 105 TonC yr−1 (11.5%), while the contribution of TOC from the Caura River to the Orinoco River was estimated at 3.05 × 105 TonC yr−1 (7.1%).The values of annual transport of TOC calculated for the Apure, Caura and Orinoco rivers were lower than those reported twenty years ago. This could be related to interannual variations of precipitation in the Orinoco Basin, due to runoff variations can have a strong effect on the fluxes of OC from land to rivers. 相似文献
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西江、北江下游及三角洲网河河道同步水文测验成果分析 总被引：1，自引：1，他引：1
1999年汛期，西江、北江下游及三角洲开展了历史上规模最大、项目最齐全的同步水文测验工作。对该次测验进行了简要的介绍，并通过对测验成果的合理性分析，论述了该成果的测验精度、上下边界条件和洪潮代表性，进而指出了珠江三角洲河网主要节点和八大口门水量分配比发生了变化及所带来的影响。 相似文献
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硫和氧同位素示踪黄河及支流河水硫酸盐来源 总被引：10，自引：0，他引：10
为了准确识别河水硫酸盐受自然风化和人为活动影响的过程,做好地表水资源管理,选择黄河小浪底水库以下干流和支流河水为主要研究对象,分期采集河水样品,采用硫酸盐硫和氧同位素,结合水化学组成及潜在硫酸盐来源硫和氧同位素范围,判定黄河及支流河水硫酸盐的来源及混入比例。结果表明:① 研究区黄河河水硫酸盐主要来源于第四纪黄土中易溶硫酸盐,干流河水SO42-含量均值为2.23 mmol/L,δ34SSO4和δ18OSO4均值分别为+8.9‰和+10.4‰;② 研究区沁河丰水期河水硫酸盐24%来源于大气降水,61%来源于土壤硫酸盐溶解,15%来自于石膏溶解;平水期河水硫酸盐39%来源于大气降水,36%来源于土壤硫酸盐溶解,25%来源于石膏溶解。沁河河水SO42-含量均值为2.44 mmol/L,δ34SSO4和δ18OSO4均值分别为+9.8‰和+9.7‰;③ 研究区洛河河水硫酸盐受生活污水影响较大,伊河河水硫酸盐受到土壤硫酸盐溶解和化学肥料溶解的共同影响,伊洛河河水SO42-含量均值为1.27 mmol/L,δ34SSO4和δ18OSO4均值分别为+10.4‰和+6.5‰。蒸发盐类矿物溶解以及土壤硫酸盐溶解等自然风化过程是控制区域河水硫酸盐来源的重要过程,人为活动对伊洛河河水硫酸盐的贡献不容忽视。 相似文献
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Yang Yueqing Tian Nong Institute of Mineral Deposits Chinese Academy of Geological Sciences Beijing Zhang Zhongming 《《地质学报》英文版》1993,67(3)
The Jinsha River-Lancang River-Nujiang River area is one of the important prospect areas for noble metal and nonferous metal deposits of China. Of a great variety of gold deposits present in this area, the following types seem to be economically most valuable and promising: tectonic alteration type in ophiolitic melange; polymetallic quartz vein type related to intermediate-acid intrusions; finely disseminated type in fracture zones; mixed hydrothermal type in tectonic fractures of carbonate rocks; hydrothermal type related to subvolcanic rocks; volcanic-hot spring type; submarine volcano exhalation-sedimentary-hydrothermal reformation type. Metallogenic epochs are exclusively Mesozoic and Cenozoic, and ore deposits and orebodies are controlled by linear structures. Magmatic activity has affected gold mineralization in varying degrees, and gold deposits are basically of mesothermal-epithermal type with ubiquitous and intense alterations. Ore-forming materials and hydrothermal solutions show multi-source character. 相似文献
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长江与黄河河口沉积物磁性特征对比的初步研究 总被引：11，自引：1，他引：10
根据2001年8月和9月分别采自黄河与长江河口沉积物样品的磁性测量和粒度分析,探讨长江和黄河河口沉积物的磁性特征及其差异。长江河口沉积物中亚铁磁性物质的含量高于黄河口,但长江口与黄河口沉积物中都是亚铁磁性矿物主导了样品磁性特征,亚铁磁性矿物晶粒都以假单畴-多畴为主。相比黄河口沉积物,长江口沉积物不完整反铁磁性物质对磁性特征的的贡献较小。长江与黄河河口的这种磁性特征主要反映了不同的沉积物来源的控制影响。此外,无论是长江口还是黄河口沉积物,磁性参数χARM、χfd%与沉积物细粒级组分存在显著的相关性,表明这两个参数作为粒度的代用指标具有普遍性。 相似文献
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The aquatic chemistry of rare earth elements in rivers and estuaries 总被引：17，自引：0，他引：17
Edward R. Sholkovitz 《Aquatic Geochemistry》1995,1(1):1-34
Laboratory experiments were carried out to determine how pH, colloids and salinity control the fractionation of rare earth elements (REEs) in river and estuarine waters. By using natural waters as the reaction media (river water from the Connecticut, Hudson and Mississippi Rivers) geochemical reactions can be studied in isolation from the large temporal and spatial variability inherent in river and estuarine chemistry. Experiments, field studies and chemical models form a consistent picture whereby REE fractionation is controlled by surface/solution reactions. The concentration and fractionation of REEs dissolved in river waters are highly pH dependent. Higher pH results in lower concentrations and more fractionated composition relative to the crustal abundance. With increasing pH the order of REE adsorption onto river particle surfaces is LREEs > MREEs > HREEs. With decreasing pH, REEs are released from surfaces in the same order. Within the dissolved (<0.22 µm) pool of river waters, Fe-organic colloids are major carriers of REEs. Filtration through filters and ultrafilters with progressively finer pore sizes results in filtrates which are lower in absolute concentrations and more fractionated. The order of fractionation with respect to shale, HREEs > MREEs > LREEs, is most pronounced in the solution pool, defined here as <5K and <50K ultrafiltrates. Colloidal particles have shale-like REE compositions and are highly LREE enriched relative to the REE composition of the dissolved and solution pools. The addition of sea water to river water causes the coagulation of colloidal REEs within the dissolved pool. Fractionation accompanies coagulation with the order of sea water-induced removal being LREEs > MREEs > HREEs. While the large scale removal of dissolved river REEs in estuaries is well established, the release of dissolved REEs off river particles is a less studied process. Laboratory experiments show that there is both release and fractionation of REEs when river particles are leached with seawater. The order of sea water-induced release of dissolved REE(III) (LREEs > MREEs > HREEs) from Connecticut River particles is the same as that associated with lowering the pH and the same as that associated with colloidal particles. River waters, stripped of their colloidal particles by coagulation in estuaries, have highly evolved REE composition. That is, the solution pool of REEs in river waters are strongly HREE-enriched and are fractionated to the same extent as that of Atlantic surface seawater. This strengthens the conclusions of previous studies that the evolved REE composition of sea water is coupled to chemical weathering on the continents and reactions in estuaries. Moreover, the release of dissolved Nd from river particles to sea water may help to reconcile the incompatibility between the long oceanic residence times of Nd (7100 yr) and the inter-ocean variations of the Nd isotopic composition of sea water. Using new data on dissolved and particle phases of the Amazon and Mississippi Rivers, a comparison of field and laboratory experiments highlights key features of REE fractionation in major river systems. The dissolved pool of both rivers is highly fractionated (HREE enriched) with respect to the REE composition of their suspended particles. In addition, the dissolved pool of the Mississippi River has a large negative Ce-anomaly suggesting in-situ oxidation of Ce(III). One intriguing feature is the well developed maximum in the middle REE sector of the shale normalized patterns for the dissolved pool of Amazon River water. This feature might reflect competition between surface adsorption and solution complexation with carbonate and phosphate anions. 相似文献
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长江与汉江现代沉积物元素组成分析 总被引：1，自引：0，他引：1
长江与汉江表层沉积物常量及微量元素组成特征分析表明,长江沉积物的常量化学组分中CaO、MgO相对较汉江高,汉江沉积物中Fe2O3、Al2O3、K2O相对较长江高;汉江沉积物的微量化学组分中Cr Ni、Mo、As、Sb、F等元素相对长江高;长江沉积物Cd的赋存形式以离子交换态和碳酸盐态为主,汉江沉积物Cd的赋存形式以残余态为主。长江沉积物与汉江沉积物组成的差异是由其源区表壳岩系决定的,前者呈现高CaO、MgO,并呈碱性(pH:8.02)的特点,而后者相对富Fe2O3,并呈中性(pH:6.8)。 相似文献
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本文以上海市苏州河沉积物为研究对象,采用Tessier形态分析法研究了沉积物中重金属元素Zn、Cu和Hg的含量变化与形态分布,初步探讨了沉积特点,对苏州河底泥的进一步治理提供了参考.结果表明,样品中Zn 、Cu、 Hg的含量匀接近或高于生物有影响水平;Zn 、Cu分别主要存在于有机态和Fe-Mn氧化物态中,可交换含量较少;Zn 、Cu、 Hg含量随沉积物浓度的变化为:沉积物表层重金属含量较低并略有起伏,中部较高,底层较低. 相似文献
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利用清政府布设在黄河中游三门峡万锦滩、沁河下游木栾店以及永定河下游石景山、卢沟桥的志桩水位记录,以首次涨水超过0.64m作为汛期建立的标志,在候尺度下恢复了其汛期建立时间距平序列。黄河中游、沁河下游和永定河下游序列分别开始于1766年、1736年和1761年。研究时段内,黄河中游和沁河下游平均在7月6~10日入汛、永定河则在7月16~20日。永定河相对较为稳定,显示出其上游雨季开始时间基本维持在7月初,而黄河中游和沁河却波动较大,早晚相差达3个月;黄河中游与沁河入汛距平波动的同相位现象在19世纪中期之后比较明显。1870~1900年代黄河中游、沁河和永定河入汛普遍延迟1个候左右,对应于黄土高原夏温偏低的时期;1820~1860年代黄河中游、沁河入汛偏早,则对应了黄土高原夏温偏高。 相似文献