塔里木盆地下奥陶统蓬莱坝组白云岩成因及储层主控因素分析——以巴楚大班塔格剖面为例   总被引：1，自引：1，他引：0  

郑剑锋  沈安江  乔占峰  倪新锋 《岩石学报》2013,29(9):3223-3232

寒武系-下奥陶统白云岩是塔里木盆地非常重要的勘探接替领域,但由于白云岩埋藏深度大,勘探和研究程度低,目前的认识程度无法满足勘探的需求,尤其是白云岩储层成因和分布的认识。本文以巴楚地区大班塔格剖面蓬莱组白云岩的精细解剖为例,测制解剖剖面9条,采集样品195块,系统的开展了岩石薄片、物性及地球化学特征分析,取得了两个方面的新的认识。1)是塔里木盆地蓬莱坝组发育粉晶、细晶、中晶和粗晶四种白云岩,主要形成于早-中埋藏期与海源流体有关的白云石化作用中,局部受到热液改造,其晶粒大小与原岩结构的粗细及孔隙空间的大小有关,原岩结构粗,形成的白云石晶粒就粗,原岩孔隙空间大,白云石晶粒就大。2)是白云岩储层的分布具成层性和旋回性,孔隙发育段总体位于向上变浅旋回的顶部,与高频旋回的暴露面有关,其载体以细-粗晶白云岩为主,孔隙主体来自原岩孔隙的继承和再调整,少量来自埋藏(热液)溶蚀作用,而并不是传统观点所认为的白云石化作用建造孔隙,这一认识对塔里木盆地深层白云岩有效储层预测具重要的指导意义。  相似文献   

白云岩之上红色粘土的磁组构特征及其成因指示意义探讨     

冯金良  朱立平 《中国岩溶》2005,24(4):270-275

通过与粉尘堆积,以及玄武岩和片麻杂岩风化剖面磁组构的对比,探讨了以贵州平坝白云岩之上红色粘土剖面磁组构特征及其成因指示意义。红色粘土的各向异性较弱,并且不具有明显的沉积磁组构;母岩的组构特征对红色粘土磁化率各向异性没有明显的控制“痕迹” ;红色粘土与粉尘堆积物之间磁组构特征的明显差异,表明它们在物源和形成机制方面是不同的;红色粘土磁化率及磁组构特征反映出红色粘土中磁性矿物的物质来源和成因具有一定的特殊性。   相似文献   

An experimental study of dissolution kinetics of Calcite, Dolomite, Leucogranite and Gneiss in buffered solutions at temperature 25 and 5°C   总被引：1，自引：0，他引：1  

S. K. Yadav  G. J. Chakrapani  M. K. Gupta 《Environmental Geology》2008,53(8):1683-1694

Laboratory experiments were carried out continuously for 30–35 days at 25 and 5°C in three different buffer solutions of pH 4.0, 2.2 and 8.4 to calculate dissolution rates of two minerals, calcite (CC) and dolomite (DM) and two rocks, leucogranite (LG) and gneiss (GN) from the Himalayan range. Calculated rates in terms of release of targeted elements versus time (Ca for CC; Mg for DM; Si for LG and GN) demonstrate direct correlation with temperature. Dissolution rates are higher at 25°C compared to 5°C. CC and DM were experimented only at pH 8.4 and results show that both undergo congruent dissolution with CC dissolving ∼5 times faster than DM. Ca and Mg exhibit average apparent activation energies (E _a) of 13.98 and 9.98 kcal mol⁻¹ respectively at pH 8.4 which reflects greater sensitivity of CC dissolution than DM dissolution towards an increase in temperature. Scanning Electron Microscope attached with Energy Dispersive X-Ray Analyser (SEM-EDX) data indicates that dissolution is controlled primarily by surface-reaction processes, with dislocation sites contributing maximum to the dissolution. As compared to CC and DM dissolution, LG and GN undergo relatively slower incongruent dissolution with precipitation of some secondary minerals as revealed from X-ray diffractometer (XRD) results. Rates of dissolution of LG is maximum at pH 2.2, moderate at pH 8.4 and least at pH 4.0, whereas GN shows maximum dissolution at pH 2.2, moderate at pH 4.0 and least at pH 8.4. A comparison in dissolution behavior of LG and GN at experimental conditions reveals that increase in Si-release rate in the temperature range between 5 and 25°C is maximum at pH 8.4 (∼3.4–4.5 times), moderate at pH 4.0 (∼3–1.8 times) and least at pH 2.2 (∼1.0–1.5 times). Within the experimental temperature range, calculated values of E _a for Si release during LG and GN dissolution advocates positive correlation with pH. A substantial decrease in initial values of Brunauer–Emmett–Teller (BET) surface area of DM, LG, and GN has been encountered at the end of the experiment, except for CC for which an increase is observed. The study clearly demonstrates the dissolution behavior of pure minerals and rocks under controlled conditions. The dissolution rates assume enormous significance for the release of trace elements from rocks/minerals to the reacting water.  相似文献   

Dolomite in caves: Recent dolomite formation in oxic, non-sulfate environments. Castañar Cave, Spain     

Ana M. Alonso-Zarza  Andrea Martín-Prez 《Sedimentary Geology》2008,205(3-4):160-164

Dolomite is a common mineral in the rock record but rare in recent superficial environments. Where it does occur, it is related to anoxic, sulfate-rich environments and microbial activity. The occurrence of some dolomite deposits in caves, however, indicates that dolomite formation is also possible in oxic, non-sulfate settings. Dolomite is forming at 17 °C and in oxic-vadose conditions on the host rocks and aragonite speleothems of the Castañar Cave, Cáceres, Spain. It appears as spheroids and dumbbells 50–300 μm in diameter that internally consist of micron-sized rhombic to rounded crystals. Initially this dolomite is Ca-rich, non-stoichiometric and poorly ordered. Mg-rich solutions allow the precipitation of metastable Mg-rich carbonates, such as huntite. This soon transforms into this Ca-rich dolomite, which later “ages” to form a more stoichiometric dolomite. These dolomites show similarities to those grown under anoxic, sulfate-rich conditions and their presence in caves provides a different setting that may contribute to the understanding of the “dolomite problem”, including their initial formation and later recrystallization processes.  相似文献   

Dissolution-precipitation reactions controlling fast formation of dolomite under hydrothermal conditions     

《Applied Geochemistry》2016

In laboratory experiments, the precipitation of dolomite at ambient temperature is virtually impossible due to strong solvation shells of magnesium ions in aqueous media and probably also due to the existence of a more intrinsic crystallization barrier that prevents the formation of long-range ordered crystallographic structures at ambient surface conditions. Conversely, dolomite can easily form at high temperature (>100 °C), but its precipitation and growth requires several days or weeks depending on experimental conditions. In the present study, experiments were performed to assess how a single heat-ageing step promotes the formation of dolomite under high-carbonate alkaline conditions via dissolution-precipitation reactions. This reaction pathway is relevant for the so-called hydrothermal dolomite frequently observed in carbonate platforms, but still ill-defined and understood. Our precipitation route is summarized by two main sequential reactions: (1) precipitation of Mg-calcite at low temperature (∼20 °C) by aqueous carbonation of synthetic portlandite (Ca(OH)₂) in a highly alkaline medium (1 M of NaOH and 1 M of MgCl₂), leading to precipitation of oriented nanoparticles of low- and high-Mg calcite (∼79 wt%) coexisting with aragonite (∼18 wt%) and brucite (∼3 wt%) after 24 h; (2) fast dolomitization process starting from 1 h of reaction by a single heat-ageing step from ∼20 to 200, 250 and 300 °C. Here, the Mg-calcite acts as a precursor that lowers the overall kinetics barrier for dolomite formation. Moreover, it is an important component in some bio-minerals (e.g. corals and seashells). Quantitative Rietveld refinements of XRD patterns, FESEM observations and FTIR measurements on the sequentially collected samples suggest fast dolomite precipitation coupled with dissolution of transient mineral phases such as low-Mg calcite (Mg < 4 mol%), high-Mg calcite (Mg > 4 mol%), proto-dolomite (or disordered dolomite; Mg > 40 mol%) and Ca-magnesite. In this case, the dolomite formation rate and the time-dependent mineral composition strongly depend on reaction temperature. For example, high-purity dolomitic material (87 wt% of dolomite mixed with 13 wt% of magnesite) was obtained at 300 °C after 48 h of reaction. Conversely, a lower proportion of dolomite (37 wt%), mixed with proto-dolomite (43 wt%), Ca-magnesite (16 wt%) and high-Mg calcite (4 wt%), was obtained at 200 °C after 72 h. The present experiments provide an additional mechanism for the massive dolomite formation in sedimentary environments (ex. deep sea organic-rich carbonate-sediments) if such sediments are subjected to significant temperature variations, for example by hot fluid circulations related to volcanic activity. In such systems, organic degradation increases the carbonate alkalinity (HCO₃⁻) necessary to induce the dolomitization process at low and high temperature.  相似文献   

≥3700 Ma pre-metamorphic dolomite formed by microbial mediation in the Isua supracrustal belt (W. Greenland): Simple evidence for early life?     

Allen P. Nutman  Clark R.L. Friend  Vickie C. Bennett  David Wright  Marc D. Norman 《Precambrian Research》2010

Chemical (meta)sedimentary rocks in the amphibolite facies ≥3700 Ma Isua supracrustal belt (W. Greenland) are mostly strongly deformed, so there is only a small chance of the survival of features such as stromatolites or microfossils that would be direct proof of a ≥3700 Ma biosphere. Therefore the search for evidence of ≥3700 Ma life in Isua rocks has focused on chemical signatures, particularly C-isotopes. The new approach presented here is based on whole rock chemistry rather than isotopic signatures. Isua chemical sedimentary rocks have Ca–Mg–Fe bulk compositions that coincide with ferroan dolomite – siderite/Fe-oxide mixtures. Most have low Al₂O₃, TiO₂ contents (<0.5 and <0.05 wt% respectively) showing minimal contamination from terriginous materials. Identical seawater-like REE + Y shale-normalised trace element signatures with La, Ce, Eu and Y positive anomalies are found in magnetite-rich banded iron formation (BIF – such as the geochemical standard IF-G), dolomite-rich rocks and quartz–carbonate–calc-silicate rocks. Additionally from a rare, small area of low deformation in Isua, there are ∼3700 Ma pillow lava interstices consisting of quartz + tremolite + calcite derived from pre-metamorphic dolomite + silica. Thus the dolomite in the chemical sediments and the pillow interstice was part of the pre-metamorphic assemblage, and was deposited from seawater and/or low-temperature groundwater (as shown by the REE + Y chemistry). Therefore, at least some Isua carbonate rocks are sedimentary or diagenetic in origin rather than being formed by metasomatism at 600–500 °C as proposed by Rose et al. (1996. American Journal of Science 296, 1004–1044).  相似文献   

江汉盆地白垩系渔洋组砂岩的成岩作用及其热力学分析   总被引：4，自引：2，他引：4  

关平张文涛  吴雪松熊金玉 《岩石学报》2006,22(8):2144-2150

江汉盆地白垩系渔洋组砂岩存在五种类型的成岩作用。其中,与油气运移有关并对储层孔隙演化产生重要影响的是硬石膏的胶结与交代作用和后期方解石再次胶结作用。为了更好的研究成岩作用发生的控制因素以及成岩环境的变化,我们通过细致的热力学推导,绘制出包含方解石、白云石和硬石膏等矿物相在内的五组分相图。通过相图分析可以看出,pH 值在成岩作用过程中有着重要的作用。方解石和白云石的胶结及交代作用代表了偏中性或碱性的成岩环境;而硬石膏的胶结及交代作用则表明成岩环境由中性或碱性向酸性转变,例如酸性的油气前锋流体的注入。另外,成岩环境中阳离子(Ca~(2 )、Mg~(2 ))和阴离子(CO_3~(2-)、SO_4~(2-))的浓度对方解石、白云石和硬石膏的胶结、溶解及交代作用也有重要影响。  相似文献   

An overview of the geology of the Transvaal Supergroup dolomites (South Africa)   总被引：1，自引：0，他引：1  

P. G. Eriksson  W. Altermann 《Environmental Geology》1998,36(1-2):179-188

 In the Neoarchaean intracratonic basin of the Kaapvaal craton, between approximately 2640 Ma and 2516 Ma, two successive stromatolitic carbonate platforms developed. Deposition started with the Schmidtsdrif Subgroup, which is probably oldest in the southwestern part of the basin, and which contains stromatolitic carbonates, siliciclastic sediments and minor lava flows. Subsequently, the Nauga formation carbonates were deposited on peritidal flats located to the southwest and were drowned during a transgression of the Transvaal Supergroup epeiric sea, around 2550 Ma ago. This transgression led to the development of a carbonate platform in the areas of the preserved Transvaal and Griqualand West basins, which persisted for 30–50 Ma. During this time, shales were deposited over the Nauga Formation carbonates in the southwestern portion of the epeiric sea. A subsequent period of basin subsidence led to drowning of the stromatolitic platform and to sedimentation of chemical, iron-rich silica precipitates of the banded iron formations (BIF) over the entire basin. Carbonate precipitation in the Archaean was largely due to chemical and lesser biogenic processes, with stromatolites and ocean water composition playing an important role. The stromatolitic carbonates in the preserved Griqualand West and Transvaal basins are subdivided into several formations, based on the depositional facies, reflected by stromatolite morphology, and on intraformational unconformities; interbedded tuffs and available radiometric age data do not yet permit detailed correlation of units from the two basins. Thorough dolomitisation of most formations took place at different post-depositional stages, but mainly during early diagenesis. Partial silicification was the result of diagenetic and weathering processes. Karstification of the carbonate rocks was related to periods of exposure to subaerial conditions and to percolation of groundwater. Such periods occurred locally at the time of carbonate and BIF deposition. Main karstification, however, probably took place during an erosional period between approximately 2430 Ma and 2320 Ma. Received: 15 September 1996 · Accepted: 12 May 1998  相似文献   

石膏对白云岩溶解影响的实验模拟研究   总被引：25，自引：2，他引：25  

黄思静  杨俊杰 《沉积学报》1996,14(1):103-109

表生到埋藏成岩作用的温度与压力（４０-１３０℃、常压－３０ＭＰａ）条件下，含膏与不含膏白云岩的溶解实验证明:在表生与相对浅埋藏的温压条件（低于７５℃，２０ＭＰａ）下，石膏（或硬石膏）的存在可不同程度地加速白云岩的溶解，随着实验温度和压力的升高，石膏（或硬石膏）对白云岩溶解的这种积极作用逐渐降低。在相对深埋藏的温压条件（高于７５℃、２０ＭＰａ）下，石膏（或硬石膏）的存在显著阻止白云岩的溶解，随着实验温度和压力的继续升高，石膏（或硬石膏）对白云岩溶解的这种消极作用也逐渐增加。从实验的这种结果可以预测，在近地表条件下和埋藏成岩作用的早期阶段，由溶解作用造成的含膏白云岩地层的次生孔隙将比不含膏的白云岩地层更为发育，因而在经历了古风化作用的地层中，含膏白云岩层更易形成良好的储层；与之相反，在相对高温高压的深埋藏成岩阶段，不含膏的白云岩地层中将更容易因酸性水的溶解作用而形成次生孔隙。因而在非蒸发沉积环境中形成的白云岩体（如正常海沉积环境的灰岩中的白云岩透镜体）更易因深埋藏溶蚀作用而形成良好的储层。  相似文献   

Detection of sinkholes using 2D electrical resistivity imaging     

Michael van Schoor   《Journal of Applied Geophysics》2002,50(4):165

Sinkholes in dolomitic areas are notoriously difficult geophysical targets, and selecting an appropriate geophysical solution is not straightforward. Electrical resistivity imaging, or tomography (RESTOM) is well suited to mapping sinkholes because of the ability of the technique for detecting resistive features and discriminating subtle resistivity variations. RESTOM surveys were conducted at two sinkhole sites near Pretoria, South Africa. The survey areas are located in the dolomites of the Lyttelton Formation, which forms part of the Malamani Subgroup and Chuniespoort Group of the Transvaal Supergroup. The survey results suggest that RESTOM is an ideal geophysical tool to aid in the detection and monitoring of sinkholes and other subsurface cavities.  相似文献