Chemical weathering and CO2 consumption in the glaciated Karuxung River catchment,Tibetan Plateau     

Fan Zhang  Xiong Xiao  Lijie Wang  Chen Zeng  Zhengliang Yu  Guanxing Wang  Xiaonan Shi 《水文研究》2021,35(8):e14330

Climate factors play critical roles in controlling chemical weathering, while chemically weathered surface material can regulate climate change. To estimate global chemical weathering fluxes and CO₂ balance, it is important to identify the characteristics and driving factors of chemical weathering and CO₂ consumption on the Tibetan Plateau, especially in glaciated catchments. The analysis of the hydro-geochemical data indicated that silicate weathering in this area was inhibited by low temperatures, while carbonate weathering was promoted by the abundant clastic rocks with fresh surfaces produced by glacial action. Carbonate weathering dominated the riverine solute generation (with a contribution of 58%, 51%, and 43% at the QiangYong Glacier (QYG), the WengGuo Hydrological Station (WGHS), and the lake estuary (LE), respectively). The oxidation of pyrite contributed to 35%, 42%, and 30% of the riverine solutes, while silicate weathering contributed to 5%, 6%, and 26% of the riverine solutes at the QYG, WGHS, and LE, respectively. The alluvial deposit of easily weathering fine silicate minerals, the higher air temperature, plant density, and soil thickness at the downstream LE in comparison to upstream and midstream may lead to longer contact time between pore water and mineral materials, thus enhancing the silicate weathering. Because of the involvement of sulfuric acid produced by the oxidation of pyrite, carbonate weathering in the upstream and midstream did not consume atmospheric CO₂, resulting in the high rate of carbonate weathering (73.9 and 75.6 t km⁻² yr⁻¹, respectively, in maximum) and potential net release of CO₂ (with an upper constraint of 35.6 and 35.2 t km⁻² yr⁻¹, respectively) at the QYG and WGHS. The above results indicate the potential of the glaciated area of the Tibetan Plateau with pyrite deposits being a substantial natural carbon source, which deserves further investigation.  相似文献   

Growth mechanisms and geochemistry of carbonate concretions from the Cambrian Wheeler Formation (Utah,USA)          下载免费PDF全文

Robert R. Gaines  John S. Vorhies 《Sedimentology》2016,63(3):662-698

Carbonate concretions provide unique records of ancient biogeochemical processes in marine sediments. Typically, they form in organic‐rich mudstones, where a significant fraction of the bicarbonate required for carbonate precipitation is supplied from the decomposition of organic matter in the sediments. As a result, carbonates that comprise concretions are usually characterized by broad ranges in δ¹³C and include values that are significantly depleted relative to seawater. This article reports results from a physical, petrographic and geochemical analysis of 238 concretions from the Wheeler Formation (Cambrian Series 3), Utah, USA, which are unusual in several respects. Most prominently, they formed in organic‐poor mudstones (total organic carbon = 0·1 to 0·5%) and are characterized by a narrow range of δ¹³C that onlaps the range of contemporaneous seawater values. Subtle centre to edge trends in δ¹³C demonstrate that concretion precipitation was initiated by local chemical gradients set up by microbial activity in the sediments, but was sustained during growth by a large pool of inorganic bicarbonate probably derived from alkaline bottom waters. The large inorganic pool appears to have been important in facilitating rapid precipitation of the concretion matrix, which occurred via both displacive and replacive carbonate precipitation during early diagenesis. Stable isotope data from cogenetic pyrite (δ³⁴S) and silica (δ¹⁸O) phases provide insight into the evolution of biogeochemical processes during concretion growth, and suggest that concretions were formed almost entirely during sulphate reduction, with only minor modification thereafter. Concretions of the Wheeler Formation appear to represent an end‐member system of concretion formation in which rapid growth was promoted by ions supplied from sea‐water. As such, they offer insight into the spectrum of processes that may influence the growth of carbonate concretions in marine sediments.  相似文献   

广东大降坪硫(铅锌)矿床岩浆热液叠加作用——来自闪锌矿Rb-Sr年龄及硫同位素的证据   总被引：2，自引：2，他引：0  

赵海杰  余长发  韩心巧  郑伟 《矿床地质》2016,35(4):795-808

广东大降坪硫(铅锌)矿床位于与岩浆作用有关的大绀山多金属矿田的中部,主矿体为赋存在震旦纪变质岩中的层状、透镜状黄铁矿矿体,最近在两个不同产状的黄铁矿矿体下部又新发现了脉状及层状铅锌矿体。文章通过对铅锌矿体的年龄及硫同位素研究,探讨其与主矿体的成因关系,获得了脉状铅锌矿体中闪锌矿的Rb-Sr等时线年龄为(88.5±3.9)Ma,即晚白垩世,与上部黄铁矿矿体的年龄(约630 Ma)相差较大,而与整个大绀山多金属矿田的成矿作用时限一致。三种不同产状的矿体硫同位素组成差异明显:层状黄铁矿矿体富集硫的轻同位素(δ34S=-10.90‰~-25.55‰),且与围岩的硫同位素范围一致,说明硫来自生物的细菌还原硫;透镜状黄铁矿矿体δ34S组成范围较宽(-9.38‰~22.69‰),具多源性硫的特征;铅锌矿体的δ34S在-7.1‰~6.4‰之间变化,硫可能来自深源岩浆,并受围岩成分混染。多方面的证据表明,大降坪黄铁矿矿体下部的铅锌矿体形成于晚白垩世的岩浆热液成矿作用,透镜状黄铁矿矿体受到岩浆热液的叠加。  相似文献   

无内标-多外标校正激光剥蚀等离子体质谱法测定磁铁矿微量元素组成   总被引：4，自引：2，他引：2  

孟郁苗  黄小文  高剑峰  戴智慧  漆亮 《岩矿测试》2016,35(6):585-594

激光剥蚀电感耦合等离子体质谱(LA-ICP-MS)常用于磁铁矿原位微量元素分析,按照校正策略不同,主要分为内标法和无内标法。内标法需要用电子探针(EMPA)预先测定磁铁矿中内标元素Fe的含量,过程较繁琐,且待测元素含量会受到内标元素含量测定的影响。本文采用铁含量较高的玄武质玻璃BCR-2G、BIR-1G、BHVO-2G和GSE-1G作为外标,避免了内标元素含量的测定,建立了无内标-多外标校正LA-ICP-MS测定磁铁矿微量元素组成的分析方法。利用该方法测定了科马提岩玻璃GOR-128g和自然岩浆磁铁矿BC 28的微量元素组成以评估方法的可靠性。结果表明,科马提岩玻璃的测定结果与推荐值及前人内标法的测定值一致,多数元素的相对标准偏差RSD5%;自然岩浆磁铁矿的测定结果与推荐值相比,多数元素的RSD7%,低于前人内标法的RSD(15%)。由此说明无内标-多外标法可以实现富铁硅酸岩或磁铁矿微量元素含量的准确校正,克服了基体效应的影响。因此,无内标-多外标法是一种原位测定磁铁矿微量元素含量的快速、准确方法,具有一定的应用潜力。  相似文献   

内蒙古东升庙和炭窑口多金属硫化物矿床铁同位素地球化学特征及其成矿指示意义     

高兆富  朱祥坤  高文革  王炳林  孙剑  罗照华  包创  唐超 《地质学报》2016,90(2):352-360

本文报道了内蒙古狼山成矿带内两个最大的铅锌多金属硫化物矿床——东升庙矿床和炭窑口矿床中黄铁矿、黄铜矿单矿物的铁同位素研究结果。东升庙矿床绢云石墨片岩中不规则状黄铁矿的铁同位素组成δ~(56)Fe_(-IRMM)值在+0.04‰~+1.11‰之间,呈现铁的重同位素富集,指示了海水中的铁以氧化态沉淀并在成岩期转化成黄铁矿的矿化过程。东升庙和炭窑口矿床富硫化物矿石中黄铁矿和黄铜矿的铁同位素组成δ~(56)Fe_(-IRMM)值的变化范围为-1.33‰~+0.08‰,具有热液成矿特征,指示金属成矿物质来源于热液流体。另外,绢云石墨片岩中脉状黄铁矿的铁同位素组成δ~(56)Fe_(-IRMM)值的变化范围为-0.39‰~-0.04‰,处于矿石黄铁矿和围岩不规则状黄铁矿之间,指示脉状黄铁矿是热液矿化的产物,并在成矿过程中混入了围岩中早先形成的富集铁的重同位素的黄铁矿。绢云石墨片岩中广泛发育的不规则状黄铁矿与赋存在绢云石墨片岩中的富硫化物矿体具有完全不同的铁同位素组成,指示热液活动对不规则状黄铁矿没有明显成矿物质贡献,因此同沉积热液活动成矿的可能性不大。结合赋存在白云石大理岩中硫化物矿体的顶、底部常见硅化的白云石大理岩角砾,本文提出后生矿化是东升庙多金属硫化物矿体的主要成矿方式。另外,东升庙矿床和炭窑口矿床的矿石硫化物具有相似的铁同位素组成特征,指示两者的成矿物质来源具有相似性。  相似文献   

湘西北寒武系沉积型镍钼矿成矿物质来源   总被引：1，自引：0，他引：1  

闫友谊 《江苏地质》2016,40(4):560-566

湘西北寒武系含矿丰富,在寒武系下统牛蹄塘组黑色岩系中赋存有磷矿、石煤、钒矿、铀矿,并有有色金属钼、镍矿及铂族元素矿物聚集。通过分析总结前人成果资料,探究镍钼矿成矿地质环境条件是在低温环境、有微生物参与及强还原环境中同生沉积,对寒武系沉积型镍钼矿成矿物质来源提出了明确的看法,即成矿物质来源于海底喷流-热水。  相似文献   

二连盆地与地沥青密切相关的砂岩型铀矿床微观矿物特征及成因分析     

王文广 《铀矿地质》2016,(5):270-278

内蒙古二连盆地产在下白垩统碎屑岩系中的砂岩型铀矿床,其矿化与地沥青密切相关,有铀矿物存在之处必有地沥青;岩石中也普遍含地沥青。笔者通过蚀刻α径迹示踪,对铀含量在(200~1770)×10~(-6)的碎屑岩进行扫描电镜分析,采用分子量计算方法确定了该地区含铀碎屑岩中的铀是以多种超显微铀矿物形式存在。其中,以赛汉高毕铀矿床为代表,铀主要形成复成分磷钙铀矿。其它铀矿床也普遍有复成分磷钙铀矿产出:巴彦乌拉矿床样品因钙含量低、硅含量高,则铀石多于复成分磷钙铀矿;道尔苏矿床以铀石和磷铀矿为主,有少量沥青铀矿及复成分磷钙铀矿;哈达图矿床主要是沥青铀矿,未见复成分磷钙铀矿。除了地沥青之外,各矿床中与铀矿物共生的主要矿物还有草莓状、鲕粒状黄铁矿。由此推断,铀矿床的可能成因是:来自盆地深部的UH_3、PH_3、CaH_2、SiH_4、FeH_2、H_2S等在伴随油气向上运移过程中,由于温度、压力降低和氧化作用而发生分解及凝聚,形成草莓状、鲕粒状黄铁矿;同时派生出含U、P、Si、Ca等的氧化物的低温热水溶液,并最终结晶析出铀矿物,形成有大量黄铁矿共生的铀矿体;而油气经过长期挥发,最终演变成地沥青,成为铀矿物的载体。  相似文献   

广东省典型矿区生态复绿遥感调查研究          下载免费PDF全文

朱俊凤  王耿明 《山东国土资源》2016,32(6)

以多期遥感数据为数据源,采用人机交互解译方法提取了广东省大宝山多金属矿、云浮硫铁矿、石菉铜矿3个典型矿区生态复绿的位置、面积、变化趋势,结合野外实地调查,查明了矿区生态复绿现状,结果表明:大宝山多金属矿共有3个生态复绿区,生态复绿面积总计约10.08万m~2;云浮硫铁矿生态复绿区主要位于东南部采场,面积总计约65.21万m~2;石菉铜矿总计有生态复绿区25.4万m~2,其中已复绿区15.4万m~2,正在复绿区10.0万m~2,还有大片区域急需复绿。最后总结了3个矿区生态复绿措施和效果,并提出值得借鉴的地方和存在的不足。该文采用的技术方法能够为其他矿区特别是大范围矿区生态复绿的快速提取提供有益的参考。  相似文献   

内蒙古新地沟金矿床黄铁矿热电性特征及深部找矿意义          下载免费PDF全文

刘华南  刘家军  李小伟  刘冲昊  代鸿章  陶银龙  王建锋  杜映东  范云飞 《中国地质》2018,45(4):819-838

内蒙古新地沟金矿是中型绿岩型金矿床,但已属于严重资源危机的矿山,急待寻找接替资源,因此对新地沟金矿床进行深部远景预测具有十分重要的意义。本文根据找矿矿物学和成因矿物学理论,利用显微镜、电子探针及热电仪系统分析新地沟金矿床不同标高和矿段中黄铁矿的热电型标型特征,研究结果表明:新地沟金矿床中黄铁矿的晶型以立方体、五角十二面体及聚形为主;热电系数变化主要集中在-331.10~340.20μV·°C~(-1)范围内,导电型多以N型为主,约占总含量的80%;成矿温度主要集中于250~340℃,属于中温矿床。黄铁矿热电性参数XNP变化范围较大,估算矿体剥蚀率为67.96%~74.31%。通过对黄铁矿导型的空间分布规律和矿体剥蚀分析表明:油篓沟矿段位于矿体中底部,向深部可能有小规模延伸,小西沟矿段钻孔ZK106在深部有较大规模的延伸,其矿化前景最好;小西沟矿段钻孔ZK102深部矿化前景次之;大汗青矿段钻孔ZK_2802其深部矿化前景较差。综合分析认为,该矿床深部具有较好的找矿潜力。  相似文献   

赣南狮吼山硫铁-钨多金属矿床H-O-S同位素组成特征     

李伟  于长琦  曾载淋  刘翠辉  贺根文  陈伟  邬思涛 《岩矿测试》2018,37(6):713-720

狮吼山硫铁-钨多金属矿床位于银坑-青塘整装勘查区北部,是赣南地区唯一大型硫铁矿床。磁黄铁矿-黄铁矿(-黄铜矿-白钨矿)矿体赋存于石炭系梓山组上段地层中含铁、含钙层位,主要形成于石英-硫化物阶段。本文通过分析原生矿石矿物中H-O-S同位素组成特征,结合Pb同位素和成矿年代测试结果,探讨成矿流体来源及成矿演化过程。矿石硫化物中δ~(34)S组成特征(-5. 50‰～-0. 20‰,集中于-3. 0‰～0. 0‰)显示,硫源以岩浆硫为主,较宽的变化范围预示成矿流体遭受了叠加和改造作用。δD-δ~(18)O同位素组成主要集中于岩浆水与变质水重叠区域(δD=-74. 4‰～-48. 0‰,δ~(18)O_(H_2O)=3. 76‰～10. 86‰),说明成矿流体以岩浆水和变质水为主,后期有少量的天水混入。综合分析认为,该矿床成矿流体主要来自深部岩浆水,岩浆热液与含钙地层的接触交代作用形成大规模变质流体,再加上少量的天水混入,流体间的不混溶作用使成矿物质在岩体与含钙层位接触部位富集沉淀,形成热液充填交代型矿床。  相似文献