原油在储层介质中的加水裂解生气模拟实验   总被引：5，自引：2，他引：5  

冯子辉  侯读杰等 《沉积学报》2002,20(3):505-509

采用高温高压热模拟实验方法,开展了原油在砂岩和火成岩储层介质中的加水裂解生气模拟实验研究.结果表明,原油开始大量裂解的温度是400℃,随模拟温度增加,甲烷相对含量增大,乙烷以上重烃气尤其是丙烷相对含量减小.其中砂岩的油水混合物裂解生气主要发生在450～500℃之间,生气窗范围小,对应的烃气产率高,火成岩的油水混合物裂解生气主要发生在450～600℃之间,生气窗范围大,对应的烃气产率小.模拟烃气的组分碳同位素分馏显著,随模拟温度增加呈变重趋势.在裂解生气过程中,水解加氢和催化作用对烃气的组成、产率和碳同位素分布有重要影响。  相似文献   

沐川太平砂岩型铼钼（饿）矿点的地质特征和矿化时代   总被引：1，自引：0，他引：1       下载免费PDF全文

曹志敏  骆耀南等 《地质学报》2002,76(1):95-99

四川沐川县民主-太平-带含钼砂岩为一新矿化类型——沉积砂岩型铼钼（锇）矿点。X-射线粉晶衍射分析结果表明其中微-细晶鳞片状含钼矿物为晶质辉钼矿；高精度质谱分析发现辉钼矿中分散元素Re和铂族元素Os含量很高，具有重要的综合利用价值；高精度Re-Os同位素测年证明辉钼矿形成年龄与含矿的中生代红物学和矿床学均具有重要的理论意义和应用价值。  相似文献   

许家窑泥河湾沉积物的环境磁学特征   总被引：3，自引：3，他引：3       下载免费PDF全文

王喜生  Lovlie Reidar  苏朴 《第四纪研究》2002,22(5):451-458

许家窑泥河湾河-湖相沉积物磁化率(k)、天然剩磁(NRM)、饱和等温剩磁(SIRM_4T)、非磁滞剩磁(ARM)及S比率(IRM_-0.3T/IRM_4T)等磁学参数与深海氧同位素的对比分析结果显示:1)许家窑泥河湾层从布容/松山界线到氧同位素阶段5(0.13MaB.P.)基本上是连续沉积,沉积速率保持在约2.45cm/103a左右;2)与同期形成的黄土高原黄土-古土壤序列类似,许家窑河-湖相层也很好地记录了当时中国北方的第四纪气候和环境特征,其典型特征为冰期时高矫顽力赤铁矿含量的显著增加,而间冰期则以低矫顽力的磁铁矿及磁赤铁矿为主要载磁矿物;3)由尝试建立的S比率时间标尺所确定的许家窑古人类遗址处的地层年代约0.5MaB.P.,与先前报道的化石的UTh绝对年龄(0.1MaB.P.)不一致;4)与k相比,S比率与SIRM更适合作为河-湖相沉积物的古气候替代性指标;5)以2.45cm/10³a的沉积速率来推算,沉积物的主要物质来源为正常的河-湖相沉积,而直接接受的类似于黄土状的粉尘并不占主导地位  相似文献   

质量传输和同位素交换:流动几何学和交换机制     

刘伟 《地学前缘》2002,9(4):423-428

耦合的质量传输和动力学限制的同位素交换模型综合考虑了平流、扩散、热液弥散 ,以及岩石与水之间的不平衡同位素交换等项因素。把耦合模型应用于 2个构造环境下的古热液系统 ,进而解释稳定同位素数据。对于造成环绕浅成侵入岩体分布的18O亏损环带的流体的流动几何学 ,以及浅部正断层流体流动的几何学 ,耦合模型提供了不同于单一同位素交换模型的解释。耦合模型也提供了关于同位素相对交换速率和同位素交换机制的信息。结果表明 ,断层带的动态重结晶促进了表面反应 ,进而便利了同位素交换 ;在化学不反应性和未变形的矿物中 ,同位素交换可能受制于固态条件下的扩散。  相似文献   

苏皖地区石炭纪海相碳酸盐岩碳和氧同位素演化规律   总被引：5，自引：2，他引：5  

林春明  凌洪飞  王淑君  张顺 《地球化学》2002,31(5):415-423

对江苏南京孔山和安徽巢湖凤凰山石炭系碳酸盐岩C、O稳定同位素进行了测定。结果表明，苏皖地区石炭系δ^13C,δ^18O记录是以4个同位素演化阶段为特征，前3个同位素演化阶段与同时代的北美石炭纪相似，仅仅是内部演化特征略有不同，这反映了区域性的沉积环境的不同变化。在金陵组下部、和州组下部、黄龙组中下部和船山组层段，δ^13C表现出明显的正漂移，这可能是受植物和生物量增长、有机碳储藏量增加所引起的。δ^18O记录总体上与δ^13C值呈相似的变化趋势。δ^18O增加记录了气候变冷和冰川作用的结果。δ^18O负漂移与气候变暖和冰川消融是一致的。在浅水潮坪环境，大气淡水的淋滤作用使δ^13C和δ^18O值明显降低。  相似文献   

湘中锡矿山锑矿床成矿物质来源的同位素示踪   总被引：14，自引：0，他引：14  

彭建堂  胡瑞忠  邹利群  刘建雄 《矿物学报》2002,22(2):155-159

本文利用放射成因同位素（Pb、Sr)和轻稳定同位素（C、O）对锡矿山超大型锑矿床的成矿物质来源进行了示踪，从物源角度揭示了其在规模成矿、元素发生超常富集的原因。研究表明，锡矿山锑矿床的成矿物质不可能是来自赋矿围岩；深部地幔和基底都卷入了该矿的成矿作用；富Sb的交代型地幔和富Sb的元古界基底为其大规模成矿提供了充足的矿源，两者是形成锡成山超大型锑矿床的前提条件。  相似文献   

Tectonic Subdivision of Dabie Orogenic Belt,Central China：Evidence from Pb Isotope Geochemistry of Late Mesozoic Basalts     

匡少平  张本仁 《中国地球化学学报》2002,21(2):147-155

It has long been debated that the Dabie orogenic belt belongs to the North China or Yangtze craton. In recent years, eastern China has been suggested, based on the Pb isotopic compositions of Phanerozoic ore and Mesozoic granitoid K-feldspar (revealing the crust Pb) in combination with Meso-Cenozoic basalts (revealing the mantle Pb), being divided into the North China and Yangtze Pb isotopic provinces, where the crust and mantle of the Yangtze craton are characterized by more radiogenic Pb. In this sense, previous researchers suggested that the pro-EW-trending Dabie crogenic belt with less radiogenic Pb in the crust was part of the North China craton. In this paper, however, the Late Cretaceous basalts in the central and southern parts of the Dabie orogenic belt are characterized by some more radiogenic Pb (²⁰⁶Pb/²⁰⁴Pb=17.936−18.349,²⁰⁷Pb/²⁰⁴Pb=15.500−15.688,²⁰⁸Pb/²⁰⁴Pb=38.399−38.775) and a unique U-Th-Pb trace element system similar to those of the Yangtze craton, showing that the Mesozoic mantle is of the Yangtze type. In addition, the decoupled Pb isotopic compositions between crust and mantle were considerably derived from their rheological inhomogeneity, implying a complicated evolution of the Dabie orogenic belt. The study was funded by the National Natural Science Foundation of China (No. 49794043) and the Open Laboratory of Constitution, Interaction and Dynamics of the Crust-Mantle System, China.  相似文献   

Stable isotopic signature of a palaeoaquifer, Mississippian Alamogordo Member limestones, Sacramento Mountains, New Mexico, USA   总被引：1，自引：0，他引：1  

YongqiangWu  Henry S. Chafetz 《Sedimentology》2002,49(2):227-235

Nine stratigraphic sections, each ≈5 m thick, were sampled from the Alamogordo Member limestones of the Lake Valley Formation, Sacramento Mountains, New Mexico, USA. Four stratigraphic sections consist entirely of lime mudstone and wackestone, whereas the other five sections have a prominent layer of crinoidal packstone about 1 m thick at their base. Stable isotopic analyses reveal that the lime muds in the sections with basal packstone layers show a downward decrease in δ¹⁸O and constant δ¹³C values, whereas those in the sections solely composed of lime mudstone and wackestone have, in general, relatively uniform δ¹⁸O and δ¹³C values. The diagenesis of the Alamogordo Member limestones was previously believed to have been governed by the downward percolation of meteoric water from a regional pre-Pennsylvanian exposure surface ≈100 m above this unit. However, the uniform δ¹³C and downward decrease in δ¹⁸O values in the lime muds in the sections with basal packstones indicate that the meteoric water ascended within the Alamogordo Member, rather than descended from the overlying exposure surface. This indicates that the basal packstones were probably a conduit for meteoric water. This is further supported indirectly by the relatively uniform δ¹⁸O and δ¹³C values of the lime mud in the sections without basal packstones. The implications are that the oxygen isotopic gradients may be used to identify palaeoaquifers, flow directions within these aquifers and that meteoric diagenesis below an exposure surface could be governed by flow through a palaeoaquifer.  相似文献   

Isotopic constraints on growth conditions of multiphase calcite–pyrite–barite concretions in Carboniferous mudstones     

R. Raiswell  S. H. Bottrell  S. P. Dean  J. D. Marshall†  A. Carr‡  & D. Hatfield 《Sedimentology》2002,49(2):237-254

Carbonate concretions in the Lower Carboniferous Caton Shale Formation contain diagenetic pyrite, calcite and barite in the concretion matrix or in different generations of septarian fissures. Pyrite was formed by sulphate reduction throughout the sediment before concretionary growth, then continued to form mainly in the concretion centres. The septarian calcites show a continuous isotopic trend from δ¹³C=?28·7‰ PDB and δ¹⁸O=?1·6‰ PDB through to δ¹³C=?6·9‰ PDB and δ¹⁸O=?14·6‰ PDB. This trend arises from (1) a carbonate source initially from sulphate reduction, to which was added increasing contributions of methanogenic carbonate; and (2) burial/temperature effects or the addition of isotopically light oxygen from meteoric water. The concretionary matrix carbonates must have at least partially predated the earliest septarian cements, and thus used the same carbonate sources. Consequently, their isotopic composition (δ¹³C=?12·0 to ?10·1‰ PDB and δ¹⁸O=?5·7 to ?5·6‰ PDB) can only result from mixing a carbonate cement derived from sulphate reduction with cements containing increasing proportions of carbonate from methanogenesis and, directly or indirectly, also from skeletal carbonate. Concretionary growth was therefore pervasive, with cements being added progressively throughout the concretion body during growth. The concretions contain barite in the concretion matrix and in septarian fissures. Barite in the earlier matrix phase has an isotopic composition (δ³⁴S=+24·8‰ CDT and δ¹⁸O=+16·4‰ SMOW), indicating formation from near‐surface, sulphate‐depleted porewaters. Barites in the later septarian phase have unusual isotopic compositions (δ³⁴S=+6 to +11‰ CDT and δ¹⁸O=+8 to +11‰ SMOW), which require the late addition of isotopically light sulphate to the porewaters, either from anoxic sulphide oxidation (using ferric iron) or from sulphate dissolved in meteoric water. Carbon isotope and biomarker data indicate that oil trapped within septarian fissures was derived from the maturation of kerogen in the enclosing sediments.  相似文献   

Constraints on the application of carbon isotope thermometry in high- to ultrahigh-temperature metamorphic terranes   总被引：7，自引：0，他引：7  

M. Satish-Kumar  H. Wada  M. Santosh 《Journal of Metamorphic Geology》2002,20(3):335-350

Nine marble horizons from the granulite facies terrane of southern India were examined in detail for stable carbon and oxygen isotopes in calcite and carbon isotopes in graphite. The marbles in Trivandrum Block show coupled lowering of δ¹³C and δ¹⁸O values in calcite and heterogeneous single crystal δ¹³C values (? 1 to ? 10‰) for graphite indicating varying carbon isotope fractionation between calcite and graphite, despite the granulite facies regional metamorphic conditions. The stable isotope patterns suggest alteration of δ¹³C and δ¹⁸O values in marbles by infiltration of low δ¹³C–δ¹⁸O‐bearing fluids, the extent of alteration being a direct function of the fluid‐rock ratio. The carbon isotope zonation preserved in graphite suggests that the graphite crystals precipitated/recrystallized in the presence of an externally derived CO₂‐rich fluid, and that the infiltration had occurred under high temperature and low f_O2 conditions during metamorphism. The onset of graphite precipitation resulted in a depletion of the carbon isotope values of the remaining fluid+calcite carbon reservoir, following a Rayleigh‐type distillation process within fluid‐rich pockets/pathways in marbles resulting in the observed zonation. The results suggest that calcite–graphite thermometry cannot be applied in marbles that are affected by external carbonic fluid infiltration. However, marble horizons in the Madurai Block, where the effect of fluid infiltration is not detected, record clear imprints of ultrahigh temperature metamorphism (800–1000 °C), with fractionations reaching <2‰. Zonation studies on graphite show a nominal rimward lowering δ¹³C on the order of 1 to 2‰. The zonation carries the imprint of fluid deficient/absent UHT metamorphism. Commonly, calculated core temperatures are > 1000 °C and would be consistent with UHT metamorphism.  相似文献