Sandstone diagenesis in the Pattani Basin (Gulf of Thailand): history of water-rock interaction and comparison with the Gulf of Mexico

In the Pattani Basin, a failed-rift basin, extensive water-rock interaction has occurred between subquartzose alluvial sandstones of Miocene age and their pore fluids. Diagenetic rates and pathways have been strongly influenced by high geothermal gradients, high CO₂ fugacities, and low pore water salinities. Depositional pore water was fresh to brackish, depending on the depositional environment of the sediments. Chloride concentrations in modern formation water are believed primarily to reflect the proportions of river and sea water in the depositional environment. However, the concentration of other important solutes and the isotopic composition of the formation waters can not be explained by roportional mixing of these two end-member waters. Dissolution of detrital plagioclase (An = 3) and K- feldspar are reactions of major significance that are reflected chemically in the Na/Cl and K/Cl ratios of the formation water. Despite the high temperature of the sandstones (120–200°C), diagenetic albite does not occur. Geochemical calculations indicate the formation water is undersaturated with respect to both orthoclase and albite. This style of feldspar diagenesis differs significantly from that of sandstones of similar composition in other basins, and has probably influenced other aspects of silicate diagenesis.Important authigenic minerals are: 1. locally abundant calcite cement (δ¹³C= −12.8, δ¹⁸O= −17.3 PDB), an early diagenetic phase that formed at about 60°C; 2. pore-filling kaolinite (δ¹⁸O= 9.9, δD= −83.5SMOW) that was closely associated with feldspar dissolution and formed over a range of temperatures; and 3. fibrous pore-lining and pore-bridging illite (δ¹⁸O = 9.8, δD = − 86.7 SMOW, the last significant cement, formed at temperatures of 120 to 150°C. Potassium/argon dates on illite indicate that sandstone diagenesis took place during a period of rapid sedimentation in the first two-thirds of the burial history.Comparison of Pattani Basin diagenesis with diagenesis of sandstones of similar age in other sedimentary basins demonstrates that chemical diagenesis, relative to mechanical compaction, has been especially rapid in the Pattani Basin. This reflects the effect of high temperatures on reaction rates. The net effect is a high average rate of porosity loss with burial (11% km).     

The roles of pedogenesis and diagenesis in clay mineral assemblages: Lower Cretaceous fluvial mudrocks,Nova Scotia,Canada

Clay mineral assemblages in alluvial mudrocks are important for paleoclimatic interpretation and for understanding burial diagenetic cementation in sandstones, but it is commonly difficult to unravel the relative importance of source weathering, pedogenesis and diagenesis in their origin. The clay mineral assemblages in fluvial overbank mudrocks from the Lower Cretaceous Chaswood Formation in central Nova Scotia, investigated by X-ray diffraction analysis of the < 2 µm fraction of 45 samples, include kaolinite, illite, vermiculite, and mixed layer kaolinite/expandable clay and mica/vermiculite. The assemblages vary with depositional facies. Wetland organic-rich mudrocks have large amounts of amorphous material and kaolinite is the dominant clay mineral. In the eastern part of the basin, where overbank mudrocks were episodically uplifted by syn-sedimentary strike-slip faulting, cumulate ultisol and alfisol paleosols are common. In the ultisols, hematite is enriched and kaolinite increases at the expense of illite in the B horizon. Alfisols contain more illite and vermiculite and the B horizon is enriched in goethite. In the western part of the basin, where thin sandstones with abundant diagenetic kaolinite cement are interbedded with the mudrocks, the distinctive clay mineral assemblage of mica/vermiculite mixed layer, vermiculite with 15.5 Å peak, and kaolinite/expandable mixed layer clay with a 17.7 Å peak is interpreted to result from bacterially-mediated oxidation of organic matter below the paleo-water table during early burial diagenesis. Deeper burial diagenesis may lead to slightly higher kaolinite crystallinity. Volcanic ash appears to alter to kaolinite/expandable mixed layer clay with a 7.9 Å peak. Comparison with the continuously subsiding and rapidly accumulated Wessex Formation of southern England, formed at a similar paleolatitude, shows the strong role of pedogenic processes and early diagenesis by meteoric water in development of clay mineral assemblages in the locally tectonically uplifted Chaswood Formation.     

Stable isotope and geochemical evidence of formation pore fluid evolution during diagenesis of Tertiary sandstones and mudrocks of the Niger Delta

Petrological data provide evidence that framboidal pyrite, Fe-carbonates and kaolinite are the major diagenetic minerals developed during burial diagenesis in the Tertiary Niger Delta sandstones and associated mudrocks. The pyrite sulphur, carbonate carbon and oxygen and kaolinite oxygen and hydrogen isotope compositions have been determined. These data (pyrite, δ³⁴S = −24.8 to 21.0‰; “siderite”, δ¹³C(PDB) = −14.7 to +5.0‰, δ¹⁸O(PDB) = −19.1 to −0.6‰; Fe-calcite, δ¹³C(PDB) = +17.5 to 17.9‰, δ¹⁸O(PDB) = −8.3 to −8.0‰; kaolinite, δ¹⁸O(SMOW) = +14.7 to 17.5‰, δD (SMOW) = −86 to −43‰) have been used to interpret the isotopic compositions of the precipitating pore fluids and/or the temperatures of mineral formation. The interpretation of these results indicate that in the deltaic depositional setting the syndepositional pore waters had a significant but variable marine influence that favoured the early formation of pyrite. Subsequently the subsurface influence of meteoric waters, showing varying degrees of modification involving organic and/or water-rock reactions, played an increasingly significant role in the development of later diagenetic cements in the sediments when abundant authigenic carbonates and kaolinites were formed.     

Loss of primary texture and geochemical signatures in speleothems due to diagenesis: Evidences from Castañar Cave, Spain

Geochemical signals from speleothems are commonly used in the investigation of palaeoenvironments. In most cases, however, little attention is paid to whether or not these signals are primary or altered by diagenesis. The speleothems of the Castañar Cave (Cáceres, Spain), which are initially formed of calcite or aragonite, have undergone a variety of meteoric diagenetic processes such as micritization and neomorphism (inversion), that collectively modify their primary features (textures, mineralogy, geochemical signals). The mean δ¹³C and δ¹⁸O values of the aragonites in the cave are −8.66 and −4.64 respectively, whereas the primary calcites have mean δ¹³C and δ¹⁸O values of −9.99 and −5.77, respectively. Following the diagenetic process of micritization, the aragonite isotopic signals averaged −7.63 δ¹³C and −4.74 δ¹⁸O and the calcite micrite signals −9.53 δ¹³C and −5.21 δ¹⁸O. Where inversion took place, some secondary calcites after the aragonite show preserved aragonite, whereas others do not. The secondary calcites without aragonite relics show isotopic values slightly higher than those of the primary calcite due to the inheritance of the aragonite signal. Where aragonite relics are preserved, the isotopic signatures are very similar to those of the aragonite micrite.In addition, the stable isotopic values and Sr and Mg contents of the speleothems became also modified by micritization and/or inversion. These diagenetic processes were driven by the changes in composition of the cave waters over time and space, but also, in the case of aragonite, by its initial unstable mineralogy.The present results highlight how important diagenesis is in caves and how the initial features of cave minerals may be lost. These changes alter the geochemical signals shown by speleothems, which may have an impact on the interpretation of the results obtained in palaeoenvironmental studies.     

Clay mineralogy, organic carbon burial, and redox evolution in Proterozoic oceans

Clay minerals formed through chemical weathering have long been implicated in the burial of organic matter (OM), but because diagenesis and metamorphism commonly obscure the signature of weathering-derived clays in Precambrian rocks, clay mineralogy and its role in OM burial through much of geologic time remains incompletely understood. Here we have analyzed the mineralogy, geochemistry and total organic carbon (TOC) of organic rich shales deposited in late Archean to early Cambrian sedimentary basins. Across all samples we have quantified the contribution of 1M and 1M_d illite polytypes, clay minerals formed by diagenetic transformation of smectite and/or kaolinite-rich weathering products. This mineralogical signal, together with corrected paleo-weathering indices, indicates that late Archean and Mesoproterozoic samples were moderately to intensely weathered. However, in late Neoproterozoic basins, 2M₁ illite/mica dominates clay mineralogy and paleo-weathering indices sharply decrease, consistent with an influx of chemically immature and relatively unweathered sediment. A late Neoproterozoic switch to micaceous clays is inconsistent with hypotheses for oxygen history that require an increased flux of weathering-derived clays (i.e., smectite or kaolinite) across the Precambrian-Cambrian boundary. Compared to previous studies, our XRD data display the same variation in Schultz Ratio across the late Neoproterozoic, but we show the cause to be micaceous clay and not pedogenic clay; paleo-weathering signals cannot be recovered from bulk mineralogy without this distinction. We find little evidence to support a link between these mineralogical variations and organic carbon in our samples and conclude that modal clay mineralogy cannot by itself explain an Ediacaran increase in atmospheric oxygen driven by enhanced OM burial.     

Dating multistage paleofluid percolations: A K-Ar and O/O study of fracture illites from altered Hercynian plutonites at the basement/cover interface (Poitou High, France)

Isotopic age determination of fluid events in basement fractures is of prime importance for the reconstruction of paleo-hydraulic regimes. However, material from fracture or wall-rock is not generally easily dated. In the case of fractures filled by minerals such as phyllosilicates, it can be expected that subsequent fluid circulation may cause partial alteration or recrystallization of the previous phyllosilicates, disturbing the isotope signature. Using a specific methodology, including the extraction process without contamination of the finest (<0.2 μm) authigenic fractions, identification of clay fractions by X-ray diffraction (XRD), scanning electron microscopy, and electron microprobe, analysis of stable isotope composition (D/H, δ¹⁸O) and K-Ar dating, fluid event ages can be estimated. This methodology was applied to the northwestern margin of the French Massif Central, where basinal brines have interacted with the sedimentary cover (infra-Toarcian formations) and the fractured Hercynian crystalline basement. During periods of unknown age, precipitates from brines sealed most basement fractures as carbonates, and a recrystallization of early Hercynian phengite (+chlorite) into illite and illite/smectite minerals occurred in the earlier fractures.XRD patterns show that the clay fraction is dominated by illite and ordered mixed-layer minerals having a relatively high amount of illite (I-S R3). In the shallowest samples beneath the paleo-surface, a late assemblage is identified as a mixture of I-S minerals, a part of them being characterized by significant amounts of swelling layers (I-S R0).The δD values of the clay fractions are fairly constant around −50 ± 10‰, but δ¹⁸O values of the same clay fractions display a wide range from 8‰ to 18‰ (SMOW). The study of the size fractions between 2 and 0.2 μm reveals a correlation between K-Ar ages and δ¹⁸O values, which cannot be related to a change in the relative amounts of clay minerals. Deep fractures (at depths of 570 and 923 m) are characterized by δ¹⁸O values around 10.3 ± 0.4‰ SMOW and old ages ranging from 253 to 272 Ma. The finest fractions (<0.2 μm) of clays located at shallow level (<300 m) beneath the paleo-surface yield the highest δ¹⁸O values (15.7-18.2‰) and the youngest K-Ar dates (188 to 198 Ma). These dates are likely to record the extensional episode and thermal anomaly related to the rifting of central Atlantic Ocean (c. 190 Ma). The other important thermal/extensional episode which affected the Aquitaine Basin, namely the opening of the Gascogne gulf at c. 120 Ma, is not detected by the K-Ar method on the clay fractions. We believe that resetting of clay-type K-Ar ages linked to recrystallization was favoured in the upper part of the basement where the ancient (Hercynian) clay minerals were destabilized by subaerial low-temperature alteration during Permo-Triassic times.From a methodologic point of view, the analytical characterization of several size fractions of clays from reactivated fractures, using both stable isotope geochemistry and K-Ar isotope geochemistry, can be considered as a powerful tool for dating fluid events when no suitable material for conventional methods is available.     

鸡西盆地下白垩统城子河组-穆棱组露头砂岩中的黏土矿物成因探讨

对鸡西盆地下白垩统城子河组—穆棱组露头砂岩中的黏土矿物进行了X-衍射分析。研究结果表明,黏土矿物主要由伊利石,高岭石和伊/蒙混层组成,组合可分为高岭石型与伊/蒙混层和伊利石型两种,根据黏土矿物组合判断露头砂岩处于中成岩阶段A期。下白垩统城子河组—穆棱组煤系地层和泥岩成岩过程中析出的有机酸是高岭石型黏土矿物组合发育的重要原因,而沉积相带水动力条件弱导致砂岩渗滤条件的变差则是伊/蒙混层和伊利石型黏土矿物组合形成的原因。     

川北阿坝地区三叠系粘土矿物特征及地质意义

分析了川北阿坝地区三叠系泥质岩的岩石矿物组合、粘土矿物类型、伊利石结晶度和镜质体反射率特征,并以此划分成岩演化阶段及变质程度。以成岩作用—极低级变质作用的研究方法,明确了阿坝地区成岩作用及极低级变质作用的上、下界限及区域分布规律:以唐克为中心的地区处于成岩作用晚期阶段,成岩作用温度200～212℃,伊利石结晶度IC≥0.42;周围地区处于极低级变质作用阶段,成岩作用温度212～222℃,伊利石结晶度IC<0.42。镜质体反射率(Ro)也具有同样的演化规律。对该地区域上成岩演化的差异及原因作如下解释:由于构造活动的远近程效应存在差异,该地区的周缘明显受到构造作用的影响,因叠加动力变质而达到极低级变质作用阶段;唐克位于阿坝地块中心,受构造作用的影响相对较小,因而处于成岩作用晚期阶段。     

Microfacies and geochemistry of the Ilam Formation in the Tang-E Rashid area, Izeh, S.W. Iran

The Ilam Formation (Santonian–Campanian in age), part of the Bangestan Group, is disconformably overlain by the Sarvak Formation and underlain by the Gurpi Formation in the Tang-E Rashid, Peyon area, Izeh (Zagros), southwest of Iran.Facies analyses indicate that the Ilam carbonates formed in four microfacies belts: tidal flat, lagoon, shoal and open marine, in a platform ramp environment. Major and minor elements and carbon and oxygen isotope values were used to determine the original carbonate mineralogy of the Ilam Formation. Petrographic evidence and elemental and oxygen and carbon isotope values indicate that aragonite was the original carbonate mineralogy in the Ilam Formation. The elemental and isotopic compositions of the Ilam carbonates also illustrate that they have stabilized in the marine phreatic environment. Variations of Sr/Ca and δ¹⁸O values versus Mn suggest that diagenetic alteration occurred in a closed system. Temperature calculation based on the oxygen isotope value of the least-altered sample indicates that the very early shallow burial fluid temperature was around 28 °C.Recognition of the exact boundary between the Ilam and Sarvak Formations is difficult, due to similar lithologies and the absence of the Surgah Formation in the study area. However, elemental and oxygen and carbon isotope analysis were used to determine the boundary between these formations. The δ¹⁸O and δ¹³C values, along with elemental results, clearly indicate a subaerial exposure surface, below which meteoric diagenesis affected the sediments.     

Geochemical and Mineralogical Characteristics of Pleistocene Lignites and Associated Sediments of Marathousa Coal Field,Central Peloponnese,Greece

The mineralogy and geochemistry data are presented for thirty-seven shales,four concretions,two carbonate sediments and seven lignites from the Marathousa coal field of the Megalopolis Basin in Greece.The argillaceous rocks consist of chlorite,illite,kaolinte,albite,quartz.opal-A,calcite and dolomite;the concretions of aragonite,gypsum and pyrite;and the carbonate rocks of calcite,quartz and illite.The mineral matter in the lignites consists of gypsum,quartz,albite,chlorite,illite,opal-A,dolomite,pyrite,and rarely calcite and kaolinite Athree-factor model explains the total variaition of major and trace elements in the argillaceous sediments.The first factor is an aluminosilicate factor and involves the following elements:Al,Si,Mg,Na,K,Ti,Mn,Nb,Y,Rb,Zn,Cu,Ni,Cr,Nband V,associated with chlorite,albite and illite.The second factor involves the elements Ca,Sr,Ba,Znand Sc and is related to carbonate lithology and mainly the carbonate concretions with gypsum.The third factor involves Fe and Ce with a weak association with Mn.The diagenesis of the Marathousa sediments and lignites was not very advanced as indicated by (a) the total thickness of the sequence (500m),(b) the presence of biogenic silica(opal-A) and (c) the age of the deposit(Pleistocene).FOr these reasons the rpresence of chlorite,illite and kaolinite in the sediments and lignite is due not to diagenetic reactions but to weathering of the flysch and metamorphic rocks at the edges of the Megalopolis Basin and transport of the weathering products(illite,chlorite,kaolinite)into the basin of deposition.The diagenetic minerals of the Marathousa sequence include pyrite,gypsum,dolomite and aragonite.     

鄂尔多斯盆地陕北地区长7砂岩储层成岩相特征研究

在大量样品测试数据与野外地质调查综合分析的基础上, 对长7储层岩石学特征、物性、孔隙结构、成岩作用、成岩阶段和成岩相等进行了研究。结果表明: 研究区长7储层处于中成岩A~B期。压实作用及碳酸盐、粘土(高岭石、伊利石、伊蒙混层)矿物胶结和硅质胶结作用是造成储层原生孔隙丧失的主要原因; 绿泥石胶结抑制孔隙充填, 长石溶蚀作用使孔隙间的连通性得到改善, 储层物性得到提高。根据成岩作用类型、强度及其对储层物性的影响划分出6种成岩相, 其中压实相、碳酸盐胶结相、粘土矿物胶结相、石英加大相、浊沸石充填相不利于储层的发育, 而长石溶蚀相、绿泥石膜胶结相对储层物性改善起了重要作用。     

Late Quaternary climatic control on erosion and weathering in the eastern Tibetan Plateau and the Mekong Basin

High-resolution siliciclastic grain size and bulk mineralogy combined with clay mineralogy, rubidium, strontium, and neodymium isotopes of Core MD01-2393 collected off the Mekong River estuary in the southwestern South China Sea reveals a monsoon-controlled chemical weathering and physical erosion history during the last 190,000 yr in the eastern Tibetan Plateau and the Mekong Basin. The ranges of isotopic composition are limited throughout sedimentary records: ⁸⁷Sr/⁸⁶Sr = 0.7206–0.7240 and ε_Nd(0) = −11.1 to −12.1. These values match well to those of Mekong River sediments and they are considered to reflect this source region. Smectites/(illite + chlorite) and smectites/kaolinite ratios are used as indices of chemical weathering rates, whereas the bulk kaolinite/quartz ratio is used as an index of physical erosion rates in the eastern Tibetan Plateau and the Mekong Basin. Furthermore, the 2.5–6.5 μm/15–55 μm siliciclastic grain size population ratio represents the intensity of sediment discharge of the Mekong River and, in turn, the East Asian summer monsoon intensity. Strengthened chemical weathering corresponds to increased sediment discharge and weakened physical erosion during interglacial periods. In contrast, weakened chemical weathering associated with reduced sediment discharge and intensified physical erosion during glacial periods. Such strong glacial–interglacial correlations between chemical weathering/erosion and sediment discharge imply the monsoon-controlled weathering and erosion.     

柴达木盆地鄂博梁Ⅲ号中新统成岩作用及沉积环境

综合运用岩石学、矿物学和元素地球化学等方法,对柴达木盆地北缘构造带鄂博梁Ⅲ号构造中新统上干柴沟组碎屑岩的成岩作用、形成环境和物质来源等进行了系统研究。发现上干柴沟组碎屑岩中碎屑颗粒间主要以点-线接触关系为主,长粒矿物被定向排列,经历过较强的压实作用。其中黏土矿物含量较高,平均达到了35.03%,主要以伊利石,绿泥石及伊-蒙混层为主。碳酸盐胶结物类型主要以方解石为主,仅含有少量白云石。碳酸盐胶结物的碳氧同位素含量测定表明,碳同位素(δ13C)分布在-6.8‰~-4.0‰之间,平均为-5.0‰;氧同位素(δ18O)分布于-11.1‰~-5.4‰,平均为-8.7‰;根据碳氧同位素含量推算古盐度Z值分布于108.34~114.89,平均值为112.77;碳酸盐沉淀温度分布在43.36℃~77.84℃,平均值为62.30℃。结合对主量元素、微量元素及有机碳含量等地球化学元素的综合分析,认为鄂博梁Ⅲ号构造带中新统上干柴沟组目前所处的成岩阶段主要为早成岩阶段B期至中成岩阶段A期,在形成早期主要以干、冷的淡水-微咸水环境为主,晚期则以要对暖、湿的淡水环境为主。     

A Reconstruction and Discussion of the Effect of Diagenetic Environment on Hydrocarbon Generation Based on Diagenetic Mineral Assemblage in Mudstone

Inorganic minerals in mudstone are composed of clay minerals,carbonate and detrital minerals.Detrital minerals(such as quartz and feldspar)are mainly original deposit.However,clay minerals(kaolinite,illite,and chlorite)and carbonate(calcite and dolomite)are mostly diagenetic minerals.Furthermore,conversion of the four kinds of clay minerals are common.The formation of clay minerals and carbonate is controlled by temperature,pressure,p H,Eh and type of cations during diagenesis.Therefore mineral assemblage can indicate the characteristics and change of diagenetic environment.In addition to inorganic minerals,there are also organic matter of different sources and chemical properties in mudstone.Traditionally,it is considered that evolution of organic matter is controlled by thermal effect.Now studies show that inorganic and organic matter can interact with each other and form clay-organic complexes.This suggest that attention should be paid to the influence of diagenetic mineral assemblage and diagenetic environment on the evolution of organic matter* Samples of mudstone from 1500-4500m of the Palaeogene in the Dongying Depression,China,were collected to investigate the changes of mudstone diagenetic environment.XRD,thin section and SEM were used to detect diagenetic minerals and assemblage characteristics.Results showed that content of detrital minerals,which are floating in mud matrix or preserved as silt laminae,is basically unchanged from shallow to deep strata.Clay minerals which are gathered as argillaceous matrix or preserved as argillaceous laminae have growth and decline relation to carbonate which mainly appear as micropoikilitic ferriferous calcite and ferriferous dolomite.All these characteristics indicate that detrital minerals are exogenetic,whereas carbonate is diagenetic minerals.Based on the SEM analysis of the clay minerals,it was found that smectite present honeycomb and reticulate structure,while illite present filiform and schistose structure and there are growth and decline relationship between them.Nevertheless,hexagonal tabular and stratified kaolinite has the highest content from 2400m to3300m.Rosette and stratified chlorite shows increase trend when the burial depth is deeper than 3300m.These characteristics indicated that clay minerals are diagenetic minerals and there are conversions among the four types.Therefore form shallow to deep,three diagenetic mineral assemblage zones can be divided based on the characteristics of carbonate and clay minerals in mudstone.Namely,smectite+illite/smectite zone in the depth of 2000-2500m;kaolinite+illite/smectite zone in the depth of 2500-3300m and illite+chlorite+carbonate zone below 3300m.Previous studies showed that kaolinite is stable under acidic conditions,while other clay minerals and carbonate are stable under alkaline conditions.Hence according to mineral assemblages feature,it was inferred that diagenetic environment of mudstonehasundergonethechangeof alkaline-acid-alkaline.For the organic matter with different chemical properties in mudstone,the hydrocarbon generation will be different in the acidic and alkaline diagenetic environment even if the conditions of temperature and pressure are the same.Therefore,for hydrocarbon generation we should not only focus on thermal effect,but also pay more attention to the differences of diagenetic environment which have great significance for the understanding of hydrocarbon generation,hydrocarbon expulsion and reservoir formation in mudstone.     

Kinetic Modeling of Diagenesis of Eogene Lacustrine Sandstone Reservoirs in the Jianghan Basin,Southeastern China

In the Tuoshi oilfield,located in the Cenozoic Jianghan Basin of southeastern China ,there have been found hydrocarbon reservoirs hosted in lacustrine sandstones of the Eogene Xingouzui Formation.The main diagenetic features identified in these sandstones include the dissolution of detrital K-feldspar and albite grains,the precipitation of quartz as overgrowths and /or cements ,and the precipitation and /or transformation of clay minerals.These diagenetic features were interpreted to have occurred in early,intermediate and late stages,based on the burial depth.The kinetics of fluid-mineral reactions and the concentrations of aqueous species au each stage of diagenesis were simulated numerically for these lacustrine sandstones,using a quasi-sta-tionary state approximation that incorporates simultaneous chemical reactions in a time-space continuum.During the early diagenetic stage,pore fluid was weakly acidic,which resulted in dissolution of K-feldspar and albite and,therefore,led to the release of K^ ,Na^ ,Al^3 and SiO2(aq) into the diagenetic fluid.The increased K^ ,Na^ ,Al^3 and SiO2(aq) concentrations in the diagenetic fluid caused the precipitation of quartz,kaolinite and illite.At the beginning of the intermediate diagenetic stage the concentration of H^ was built up due to the decomposition of organic matter,which was responsible for further dissolution of K-feldspar and albite and pre-cipitation of quartz,kaolinite,and illite.During the late diagenetic stage,the pore fluid was weakly alkaline,K-feldspar became stable and was precipitated with quartz and clay minerals.When the burial depth was greater than 3000 m,the pore fluids became supersaturated with respect to allbite,but undersaturated with respect to quartz,resulting in the precipitation of albite and the dissolution of quartz.The diagenetic reactions forecasted in the numerical modeling closely matched the diagenet-ic features identified by petrographic examination, and therefore,can help us to gain a better understanding of the diagenetic processes and associated porosity evolution in sandstone reservoirs.     

广西东攀剖面二叠系顶部粘土矿物特征及古气候意义

对广西东攀剖面二叠系顶部20个样品中的粘土矿物进行X射线衍射分析。伊利石结晶度值显示这些样品形成于中晚成岩带的地质环境;伊利石、蒙脱石纵向分布规律和伊利石结晶度与伊利石含量的关系表明伊利石除陆源碎屑来源外,可能有部分为蒙脱石伊利石化而成;伊利石结晶度变化曲线和伊蒙混层类型的变化规律表明,本区粘土矿物组合与含量的变化除受到后期成岩作用的影响外,还明显地受沉积因素的控制;伊利石结晶度、伊利石化学指数、高岭石和伊利石的含量、伊蒙混层类型显示东攀剖面以9、10层界线上方5cm为界,古气候由干冷变为湿暖;水介质由偏碱性向酸性转变。     

Geothermometry, geochronology, and mass transfer associated with hydrothermal alteration of a rhyolitic hyaloclastite from Ponza Island, Italy

A rhyolitic hyaloclastite from Ponza Island, Italy, was hydrothermally altered, producing four distinct alteration zones based on X-ray diffraction mineralogy and field textures: (1) nonpervasive argillic zone; (2) propylitic zone; (3) silicic zone; and (4) sericitic zone. The unaltered hyaloclastite is volcanic breccia with clasts of vesiculated obsidian in a matrix of predominantly pumice lapilli. Incomplete alteration of the hyaloclastite resulted in the nonpervasive argillic zone, characterized by smectite and disordered opal-CT. The other three zones exhibit more complete alteration of the hyaloclastite. The propylitic zone is characterized by mixed-layer illite-smectite (I-S) with 10 to 85% I, mordenite, opal-C, and authigenic K-feldspar (akspar). The silicic zone is characterized by I-S with ≥90% I, pure illite, quartz, akspar, and occasional albite. The sericitic zone consists primarily of I-S with ≥66% I, pure illite, quartz, and minor akspar and pyrite. K/Ar dates of I-S indicate hydrothermal alteration occurred at 3.38 ± 0.08 Ma.Oxygen isotope compositions of I-S systematically decrease from zones 1 to 4. In the argillic zone, smectite has δ¹⁸O values of 21.7 to 22.0‰ and I-S from the propylitic, silicic, and sericitic zones ranges from 14.5 to 16.3‰, 12.5 to 14.0‰, and 8.6 to 11.9‰, respectively. δ¹⁸O values for quartz from the silicic and sericitic zones range from 12.6 to 15.9‰. By use of isotope fractionation equations and data from authigenic quartz-hosted primary fluid inclusions, alteration temperatures ranged from 50 to 65°C for the argillic zone, 85 to 125°C for the propylitic zone, 110 to 210°C for the silicic zone, and 145 to 225°C for the sericitic zone. Fluid inclusion data and calculated δ¹⁸O_water values indicate that hydrothermal fluids were seawater dominated.Mass-transfer calculations indicate that hydrothermal alteration proceeded in a relatively open chemical system and alteration in the sericitic zone involved the most extensive loss of chemical species, especially Si. Systematic gains in Mg occur in all alteration zones as a result of I-S clay mineral formation, and systematic losses of Na, Ca, and K occur in most zones. With the exception of Ca, calculations of mass transfer associated with hydrothermal alteration on Ponza agree with chemical fluxes observed in laboratory experiments involving hydrothermal reactions of rhyolite and seawater. The anomalous Ca loss at Ponza may be due to hydrothermal formation of anhydrite and later low-temperature dissolution. On the basis of Mg enrichments derived from circulating seawater, we estimate the following minimum water/rock ratios: 9, 3, 6, and 9 for the argillic, propylitic, silicic, and sericitic zones, respectively. Hydrothermal fluid pH for the propylitic and silicic zones was neutral to slightly basic and relatively acidic for the sericitic zone as a result of condensation of carbonic and perhaps other acids.     

Mineralogy and major-element geochemistry of the lower Permian Greta Seam,Sydney Basin,Australia

The mineralogy of the high-volatile bituminous coals and associated strata from the Greta seam, Sydney Basin, Australia, has been evaluated in this study. Although the seam is not immediately overlain by marine strata, percolation of marine water into the original peat bed is indicated by the petrological, mineralogical and geochemical characteristics, which resemble those of coals with marine roof strata. The upper and lower sections of the seam have contrasting mineralogy. Pyrite typically comprises 40 to 56 wt% of the mineral assemblage in the marine-influenced upper part of the seam section. The lower part contains much less pyrite (typically <5 wt%, organic-free basis), and also relatively abundant dawsonite (up to 14 wt%, organic-free basis). The minerals within most coal plies are largely of authigenic origin. These include pyrite, siderite, clay minerals (mainly kaolinite and Na-rich mixed-layer illite/smectite), and quartz, most of which have a relatively early, syngenetic origin. Minor Ti-bearing minerals, anatase or rutile, and phosphate minerals, fluorapatite and goyazite, were probably also formed during early diagenesis. Other minerals have features that indicate late-stage precipitation. These include abundant cleat- and fracture-filling dawsonite, which may be the result of reactions between earlier-precipitated kaolinite and Na₂CO₃- or NaHCO₃-bearing fluids. Minor albite may also be epigenetic, possibly precipitated from the same Ca–Al bearing fluids that formed the dawsonite. The most abundant detrital minerals in the Greta coals are quartz, poorly ordered kaolinite, illite and mixed-layer illite/smectite (I/S). These occur mainly in the floor, roof and other epiclastic horizons of the seam, reflecting periods of greater clastic influx into those parts of the original peat-forming environment. Detrital minerals are rare in the coals away from the epiclastic horizons, probably owing to almost complete sediment bypassing in the depositional system. Alternatively, any detrital minerals that were originally present may have been leached from the peat bed by diagenetic or post-diagenetic processes.     

辽河盆地西部凹陷粘土矿物的成岩作用研究

对辽河盆地西部凹陷兴隆台、马圈子、欢喜岭和曙光等地沙河街组不同深度的层位,高升地区(属弱碱性和弱氧化-弱还原环境的沙四段分别采样,经X-光衍射、电子显微镜、化学分析和差热、红外等项目的分析鉴定,研究区内的粘土矿物有: 蒙脱石 在全区较浅的地层(如欢喜岭地区小于1000米,兴隆台地区小于1500米)中均有分布。其主要成份为二八面体的钙蒙脱石。 皂石 为黑色橄榄-辉石玄武岩的次生产物。     

辽河坳陷古近系碎屑岩储层孔隙演化特征探讨

辽河坳陷古近系的沉积特征是物源多、沉积体系多、砂岩成熟度低及砂体规模小。通过成岩作用和成岩相研究,储层成岩相可划分为4种,即碳酸盐胶结相、自生粘土矿物胶结相、石英胶结相和粘土矿物转化相。这4个相可进一步划分为7个亚相：自生粘土膜胶结亚相、晶粒状碳酸盐胶结亚相、自生高岭石胶结亚相、石英胶结亚相、嵌晶状碳酸盐胶结亚相、伊/蒙混层亚相和伊利石亚相。不同成岩相分布明显受深度控制,具有在垂向相连的展布特征,垂向上可组成6个成岩相带。通过大量的砂岩和泥岩孔渗数据统计分析,建立了6个对应的高孔渗带（ABCDEF）与6个低孔渗带（abcdef）,它们与6个成岩相带在空间分布上具有一一对应关系,即A－a、B－b、C－c、D－d、E－e和F－f分别与晶粒状碳酸盐相带、自生高岭石相带、石英胶结相带、嵌晶状碳酸盐相带、伊／蒙混层粘土矿物相带和伊利石相带相对应。可见,不同成岩相带对应不同孔隙度发育带的孔隙演化,并从有机质演化的角度解释了上述对应关系。应用这一规律在鸳鸯沟地区有利储层孔隙预测中取得了较好效果,验证了该区储层孔隙演化特征及其对油气运聚的影响。