滇东北火德红铅锌矿床地球化学特征与成矿机制分析   总被引：1，自引：0，他引：1  

武昱东  王宗起  罗金海  程家孝  张英利  王师迪 《矿床地质》2016,35(5):1084-1098

文章通过研究滇东北火德红铅锌矿床岩石地球化学和S、Pb同位素地球化学特征,分析其成矿金属和成矿流体来源,进而对其成矿机制进行探讨。围岩主量与微量元素分析结果表明,火德红铅锌矿床为后生热液矿床,铅锌等成矿金属物质随热液进入赋矿围岩,结合围岩蚀变特征判断,其应属中_低温热液成因;闪锌矿与黄铁矿的δ34S主要分布在-17‰~-11.4‰,其S源极可能来自生物成因硫酸盐还原,与川滇黔地区铅锌矿的S同位素来源(总体来自海水硫酸盐热化学还原)有着明显的不同;矿石硫化物的Pb同位素比值变化范围较窄,均为正常Pb;Pb同位素主要来自于上地壳,有少量岩浆物质混入。上述特征表明火德红铅锌矿床为构造和岩性共同控制的后生热液型矿床,其成矿机制与典型MVT型铅锌矿相似。  相似文献   

广西官村岩溶溪流中生物地球化学控制的DIC和NO3-昼夜变化研究     

张陶  蒲俊兵  袁道先  李建鸿 《地质学报》2016,90(8):1965-1976

为了解岩溶区控制溪流中溶解无机碳(DIC)和NO_3~-昼夜变化的生物地球化学过程以及DIC和NO_3~-日变化量,于2014-07-22~2014-07-24期间,在广西壮族自治区融安县官村溪流中包括地下河出口(CK)和下游雷崖村(LY)设置两个监测点同时对水体物理化学参数以及C、N同位素(δ~(13) CDIC、δ~(15) N-NO_3~-和δ~(18) O-NO_3~-)展开了为期2d的高分辨率昼夜监测采样工作。结果发现CK点各物理化学参数没有表现出昼夜变化,但是LY点Ca2+、DIC以及PCO2表现出明显的昼夜变化规律,即白天下降夜间上升且与DO和pH表现出明显的负相关关系。相对于CK点,在白天水生光合生物光合作用导致LY点DIC下降的同时δ~(13) CDIC上升,而在夜间呼吸作用导致LY点DIC上升的同时δ~(13) CDIC下降且部分时间段要低于CK点δ~(13) CDIC值。溪流中的NH4+在监测期间基本上都在下降而NO_3~-离子在夜间和上午时间段都在上升,δ~(15) N-NO_3~-却表现出下降的趋势,且比较接近δ~(15) N-NO_3~-初始值,而NO_3~-离子在下午时间段出现下降的趋势。结果表明溪流中DIC昼夜变化主要受到水生植物的光合作用和呼吸作用控制,且通过质量平衡方程计算得知溪流中由于光合作用吸收无机碳而转为有机碳的量为0.94kgC/d,这部分有机碳可以形成相对长期稳定的自然C汇。溪流在夜间和上午时间段发生了N的硝化作用,增长量为2.08kgN/d,但在下午时间段(12:00~18:00)发生了N的同化作用,损失量为0.42kgN/d。溪流输出的NO_3~--N的量为1.66kgN/d,表明在富碳、富钙的岩溶溪流中,有利于水生光合生物的生长,促进N的同化作用的发生,从而减少溪流输出NO_3~--N的量,说明岩溶区溪流N的生物地球化学过程可能在昼夜尺度上改变水质。  相似文献   

鄂尔多斯盆地北部直罗组有机质特征及与铀成矿关系   总被引：2，自引：0，他引：2  

侯惠群  李言瑞  刘洪军  韩绍阳  王贵  白云生  吴迪  吴柏林 《地质学报》2016,90(12):3367-3374

本文研究了鄂尔多斯盆地典型铀矿床的有机质与铀成矿的关系。探讨了煤屑的赋存状态、煤质特征及成熟度,认为煤屑的演化程度均较低,处于低成熟阶段,有利于对铀的吸附。总体上看煤质有机质和铀矿化关系密切,铀含量与煤屑含量呈正相关关系,对铀矿物为吸附态形式。通过对该区油气包裹体的研究认为,该区存在多期次的成岩方解石胶结过程,并伴随多期次的油气包裹体发育,尤以晚期的胶结方解石矿物中存在丰富的晚期油气包裹体。研究认为晚期可能发生过油、气的运移和聚集,铀矿床的形成与赋矿砂岩中有机流体或还原性气体的充注和络合作用密切相关,因而这些丰富的有机流体和还原性气体对于铀的富集沉淀具有重要意义。  相似文献   

Re-parameterization of a quasi-analytical algorithm for colored dissolved organic matter dominant inland waters     

《International Journal of Applied Earth Observation and Geoinformation》2016

Quasi-Analytical Algorithms (QAAs) are based on radiative transfer equations and have been used to derive inherent optical properties (IOPs) from the above surface remote sensing reflectance (R_rs) in aquatic systems in which phytoplankton is the dominant optically active constituents (OACs). However, Colored Dissolved Organic Matter (CDOM) and Non Algal Particles (NAP) can also be dominant OACs in water bodies and till now a QAA has not been parametrized for these aquatic systems. In this study, we compared the performance of three widely used QAAs in two CDOM dominated aquatic systems which were unsuccessful in retrieving the spectral shape of IOPS and produced minimum errors of 350% for the total absorption coefficient (a), 39% for colored dissolved matter absorption coefficient (a_CDM) and 7566.33% for phytoplankton absorption coefficient (a_phy). We re-parameterized a QAA for CDOM dominated (hereafter QAA_CDOM) waters which was able to not only achieve the spectral shape of the OACs absorption coefficients but also brought the error magnitude to a reasonable level. The average errors found for the 400–750 nm range were 30.71 and 14.51 for a, 14.89 and 8.95 for a_CDM and 25.90 and 29.76 for a_phy in Funil and Itumbiara Reservoirs, Brazil respectively. Although QAA_CDOM showed significant promise for retrieving IOPs in CDOM dominated waters, results indicated further tuning is needed in the estimation of a(λ) and a_phy(λ). Successful retrieval of the absorption coefficients by QAA_CDOM would be very useful in monitoring the spatio-temporal variability of IOPS in CDOM dominated waters.  相似文献   

赛里木湖沉积物有机质变化特征及其环境信息   总被引：3，自引：0，他引：3  

陈京  吉力力·阿不都外力  马龙 《冰川冻土》2016,38(3):761-768

在分析赛里木湖湖泊沉积物中氮含量(TN)、有机碳含量(TOC)及其碳同位素(δ~(13)C_(org))以及色素等指标的变化特征的基础上,结合沉积物中有机指标的环境意义的探讨,揭示了新疆赛里木湖湖泊沉积物中有机质所蕴含的环境信息.赛里木湖沉积物中总有机碳含量、总氮含量的变化反映了流域初级生产力的变化,沉积物色素变化是有机质保存条件的指标,间接指示了湖泊-流域水热配置环境.有机碳同位素(δ~(13)C_(org))反映了湖泊内外源的混合信息.结合有序样品聚类分析方法,可以将赛里木湖近代环境划分为四大发展阶段:1、各有机指标相对稳定;2、各有机指标明显波动;3、各有机指标显著增加;4、各有机指标快速增加.  相似文献   

黄河三角洲滨海湿地演化过程中的碳埋藏效率及其控制因素          下载免费PDF全文

丁喜桂  王吉松  赵广明  袁红明  王锦  叶思源 《中国地质》2016,(1):319-328

2007年在黄河三角洲布设了一口浅钻ZK4,孔深28.3 m,对获取的岩心样品进行了详细的沉积学观测及含水量、有机碳、总碳和营养成分的实验室分析测试。通过ZK4孔的地层分析,将其划分为7种沉积环境,揭示了滨海湿地地质演化过程。并利用AMS14C测年方法,结合黄河改道的历史记录,运用历史地理学和沉积地质学综合分析的方法对黄河三角洲沉积环境进行了年代划分,并计算了黄河三角洲不同沉积环境沉积物的沉积速率和碳的加积速率。结果表明:总碳和有机碳与除硫和磷元素以外的各营养成分都呈良好的线性相关;碳、氮、磷的加积速率与沉积物的沉积速率呈极显著正相关关系(R0.89,p0.01),沉积物的沉积速率是碳、氮、磷的加积速率的主控因素;虽然现代黄河三角洲沉积物有机碳浓度较低(1%),但由于沉积物的高沉积速率,现代黄河三角洲沉积物有机碳的平均加积速率达到2878.23 g/(m2·a),远高于世界其他高有机碳浓度的湿地,因此是很好的碳汇地质体。  相似文献   

贵州织金下寒武统黑色页岩矿物岩石成分及资源利用特征     

王沙  张杰 《岩石矿物学杂志》2016,35(3):543-552

通过野外采样、化学分析、电子探针(EPMA)和X射线衍射(XRD)分析等手段,研究了贵州织金地区黑色页岩矿物成分、化学组分、微量元素、稀土元素特征。研究区矿样化学成分以SiO_2和Al_2O_3为主,且具有高K低Na的特征。电子探针和X射线衍射分析表明,研究区黑色页岩主要矿物组成有石英、粘土矿物、白云石及黄铁矿等。织金黑色页岩中Pb、Ni、U、V、Cr等金属元素存在不同程度的富集,稀土元素总量为153.2×10~(-6)~224.89×10~(-6),属轻稀土元素富集型。同时从多金属层、页岩气、页岩提钾及近底部含磷铀矿资源等方面讨论了织金黑色页岩资源化利用。织金黑色页岩多金属层含有Mo、V、Ni、Ag及U等多金属元素,具综合利用价值;其中有机碳含量达到页岩气开发大于2%的条件,可进一步开展研究;页岩中伊利石含量较多,可提取黑色页岩中的钾制备含钾复合肥;黑色页岩底部与磷矿层接触带产出磷铀矿,主要为胶状磷铀矿,接触带可作为铀矿找矿的标志层。  相似文献   

CMIP5地球系统模式溶解氧模拟结果分析     

鲍颖  李阳春 《海洋学报(英文版)》2016,35(12):28-37

本文基于常用的统计方法,通过与WOA09观测的海洋溶解氧浓度数据进行比较,定量地评估了9个CMIP5地球系统模式在历史排放试验中海洋溶解氧气候态特征的模拟能力。在海表,由于地球系统模式均能很好地模拟海表温度（SST）,模式模拟的海表溶解氧浓度分布与观测一致,模拟结果无论是全球平均浓度偏差还是均方根误差均接近0,空间相关系数与标准偏差接近1。在海洋中层以及深层这些重要水团所在的区域,各模式的模拟能力则差异较大,尤其在溶解氧低值区（OMZs）所在的500m到1000m,各模式均出现全球平均偏差、均方根误差的极大值以及空间相关系数的极小值。在海洋内部,模式偏差的原因比较复杂。经向翻转环流和颗粒有机碳通量均对模式的偏差有贡献。分析结果表明物理场偏差对溶解氧偏差的贡献较大。一些重要水团,比如北大西洋深水,南极底层水以及北太平洋中层水在极大程度上影响了溶解氧在这些海区的分布。需要指出的是,虽然在海洋内部各模式模拟的溶解氧浓度偏差较大,但是多模式平均结果却能表现出与观测较好的一致性。  相似文献   

A novel method to estimate mineral compositions of mudrocks: A case study for the Canadian unconventional petroleum systems     

《Marine and Petroleum Geology》2016

The mineral composition of mudrocks is an essential attribute in controlling the reservoir quality of unconventional petroleum systems. The present study introduces a semi-quantitative method to estimate mineral phases of mudrocks in various Canadian unconventional hydrocarbon systems using total elemental analysis (inductively coupled plasma-mass spectrometry (ICP-MS)) and Rock-Eval data (total organic carbon (TOC) and mineral carbon (MinC)).This method involves statistical analysis based on a sound knowledge of hydrocarbon source rock inorganic geochemistry. The workflow can be divided into four steps: (i) converting major elements (Si, Al, Fe, K, Na, Ca, Mg, Ti, and P) to their oxides, (ii) inferring modes of occurrence of elements using statistical analysis of geochemical data (major elements, TOC, and MinC), (iii) identifying the mineral types (oxide, aluminosilicates, carbonates, sulfide, and phosphate) according to elemental occurrences and calculating mineral phase concentrations, and (iv) verifying the results by comparing to XRD data on selected samples. The results, especially for brittle minerals such as quartz, carbonates (e.g. calcite, dolomite, and ankerite), and pyrite, show that the estimated mineral compositions correspond closely and consistently with measured mineralogy obtained from XRD. This method takes advantage of bulk geochemical data already available for hydrocarbon potential and chemostratigraphic studies, without devoting additional samples and cost for XRD analysis.  相似文献   

Copper Speciation in a Collection of Geochemical Reference Materials Using Sequential Extraction and Evaluation of the Validity Using XANES Spectroscopy          下载免费PDF全文

Atsuyuki Ohta  Ran Kubota 《Geostandards and Geoanalytical Research》2016,40(1):117-134

Copper speciation in a collection of Japanese geochemical reference materials (JSO‐1, JLk‐1, JSd‐1, ‐2, ‐3 and ‐4, JMs‐1 and JMs‐2) was achieved by sequential extraction and characterised using X‐ray absorption near‐edge structure spectroscopy. In the first step of the extraction, referred to as the acid fraction, between 1% and 20% total Cu within the reference materials was extracted. Such a result is typically accounted for by absorption of Cu onto clay minerals. However, the presence of Cu sulfate (an oxidation product of chalcopyrite) was observed in some of the stream sediments affected by mining activity (JSd‐2 and JSd‐3) instead. Copper was extracted in the reducible fraction (targeting Fe hydroxide and Mn oxide) (2–49% total Cu). Between 2% and 51% Cu was extracted in the oxidised fraction (targeting sulfides and organic matter). X‐ray absorption near‐edge structure spectroscopy clarified that the reducible fraction consisted of Cu bound to Fe hydroxide, whereas the oxidised fraction was a mixture of Cu bound to humic acid (HA) and Cu sulfide. In the oxidisable fraction, chalcopyrite was the predominant species identified in JSd‐2, and Cu bound to HA was the major species identified in JSO‐1 (a soil sample).  相似文献