Origin of subaerial Holocene calcareous crusts: role of algae, fungi and sparmicritisation

The Pleistocene Miami Limestone that crops out on the lower Florida Keys is overlain by thin (16 cm or less), discontinuous, Holocene calcareous crusts (caliche) that are usually laminated, composed dominantly of calcite micrite and may or may not incorporate part of the underlying limestone. Both allochems and sparry calcite cement in the former unit contain endolithic algae and fungi, borings and unicellular algae. Biogenic structures identical to those in the Miami Limestone also occur in the calcareous crusts but are somewhat less abundant in the latter unit versus the former unit. The calcareous crusts were formed in the vadose diagenetic environment. Some of the CaCO₃ necessary for the micrite that comprises the bulk of the crusts was probably derived from solution of carbonate from a soil cover and some from wind blown salt spray. Most of the micrite, however, was formed by replacement of the uppermost portions of the Miami Limestone. Replacement involved micritisation of allochems and a previously unreported process, sparmicritisation, the degrading recrystallization of sparry calcite to micrite. Minor sparmicritisation was caused by micrite calcification of endolithic fungi or algae within sparry calcite cement or by micrite precipitation in empty borings within such cement. Most sparmicritisation took place by dissolution of sparry calcite and concomitant precipitation of micrite in the space occupied previously by the dissolved spar. Such sparmicritisation is interpreted to be caused by chemical reactions involving the crystals, pore water which is moving slowly but steadily and organic compounds released during bacterial decomposition of fungi, algae or both. It is recognized that sparmicritisation occurs in the marine diagenetic environment and is not, therefore, necessarily indicative of vadose diagenesis. Incomplete sparmicritisation is responsible for some of the clotted textures typically found within calcareous crusts and may explain such textures in many other carbonate rock types. A combination of sparmicritisation and micritisation has probably greatly influenced the porosity of many reefs and, in some cases, led to the formation of ‘micritic reefs’.     

酒西盆地碎屑岩胶结物的形成问题

酒西盆地下白垩统陆相碎屑岩胶结物的形成关系到油气储集的重要问题,富铁的洪积扇沉积体系和非富铁的河流一湖泊沉积体系形成两种不同的胶结物组合类型,平面上可分为三带胶结物:混合胶结带、铁镁胶结带和浓聚成岩带。盆地边缘带是以铁、泥、钙为主的混合胶结物,中间为以碳酸铁镁矿物的白云石、铁白云石为主的胶结物,盆中带形成胶结物的浓聚成岩层,事实证明过渡的铁镁胶结带是最富于聚集油气的地带。本文还在纵向上探讨了泥质粘土矿物和碳酸盐胶结物的成岩变化。     

地层水条件下碳酸盐矿物热力学平衡条件及其在克拉2气田的应用

基于热力学平衡理论及库车盆地的实际,建立了该区地层水温度、压力条件下方解石溶解、白云石对方解石交代作用的热力学平衡条件,并根据地层水介质特征探讨了该区方解石溶解、白云石交代方解石的具体成岩反应状况,认为该区地层水条件下正进行着方解石溶蚀及白云石对方解石的交代作用,方解石的溶蚀是形成该区深层次生孔隙的根本因素。      

Late Pleistocene mixing zone dolomitization, southeastern Barbados, West Indies

ABSTRACT Field, geochemical, and petrographic data for late Pleistocene dolomites from southeastern Barbados suggest that the dolomite precipitated in the zone of mixing between a coastal meteoric phreatic lens and normal marine waters. The dolomite is localized in packstones and wackestones from the algalAmphistegina fore-reef calcarenite facies. Stable isotopic evidence suggests that meteoric water dominated the diagenetic fluids responsible for dolomitization. Carbon isotopes in pure dolomite phases average about -15%₀ PDB. This light carbon is attributed to the influence of soil gas CO₂, and precludes substantial mixing with seawater. A narrow range of oxygen isotopic compositions coupled with a wide range of carbon compositions attest to the meteoric diagenetic overprint. Dolomitization likely occurred with as little as a five per cent admixture of seawater. Strontium compositions of the dolomites indicate probable replacement dolomitization of original unstable mineralogy. The dolomite is characterized by low sodium values. Low concentrations of divalent manganese and iron suggest oxidizing conditions at the time of dolomitization. A sequence of petrographic features suggests a progression of diagenetic fluids from more marine to more meteoric. Early marine diagenesis was followed by replacement dolomitization of skeletal grains and matrix. Limpid, euhedral dolomite cements precipitated in primary intra- and interparticle porosity subsequent to replacement dolomitization. As waters became progressively less saline, dolomite cements alternated with thin bands of syntaxial calcite cement. The final diagenetic phase precipitated was a blocky calcite spar cement, representing diagenesis in a fresh-water lens. This sequence of diagenetic features arose as the result of a single fall in eustatic sea-level following deposition. A stratigraphic-eustatic-diagenetic model constrains both the timing and rate of dolomitization in southeastern Barbados. Dolomitization initiated as sea-level began to fall immediately following the oxygen isotope stage 7–3 high stand, some 216 000 yr bp . Due to the rapidity of late Pleistocene glacio-eustasy, dolomitization (locally complete) is constrained to have occurred within about 5000 yr.     

Magnesian calcite cements and their diagenesis: dissolution and dolomitization, Mururoa Atoll

The most ubiquitous syn-sedimentary cements affecting Mururoa atoll are composed of magnesian calcite. Three main types are distinguished: fibrous, bladed and sparitic on the basis of petrography, morphology and MgCO₃ concentration of the constituting crystals, while peloid infills, a particular form of HMC chemical precipitation, also exist. Petrographic evidence and isotopic signatures are compatible with marine precipitation. Mururoa atoll was exposed several times to meteoric diagenesis resulting in varied diagenetic alterations including selective dissolution and partial dolomitization of Mg-calcite cements. These alterations are responsible for substantial modifications of the initial cement fabrics and may introduce unconformities in the diagenetic chronology. The first stage of the partial dissolution of Mg-calcite induces the development of chalky, white friable zones within the initially crystalline, hard cement layers. At ultrascale, this is due to the creation of micro-voids along the elongate cement fibres. Advanced dissolution includes total disappearance of cement portions as attested to by large voids within the cement crust and/or between superposed cement layers. Mg-calcite dissolution is related to meteoric diagenesis during periods of Quaternary exposure. The creation of voids within Mg-calcite layers is due to the mechanical removal of previously altered calcium carbonate, a process suggesting marine or non-marine water flow, probably in the vadose environment. Selective dolomitization of Mururoa cements involves alternations of calcite and dolomite which form successive cement-like rinds within primary cavities. At Mururoa, these alternations are the result of selective dolomitization of the pre-existing Mg-calcite cements rather than successive precipitation of calcite and dolomite. Selective dolomitization of Mg-calcite cements at Mururoa indicates that a given cement succession is not necessarily a simple chronological sequence. Oxygen isotope values of dolomites are enriched in δ¹⁸6 by about 3‰ PDB within calcite-dolomite pseudo-alternations. The dolomitizing fluid at Mururoa seems similar to present marine water although some mixture with meteoric water is probable to favour dissolution associated with dolomitization.     

The dolomitization of CaCO3: an experimental study at 252–295°C

The results of experiments on the hydrothermal dolomitization of calcite (between 252 and 295°C) and aragonite (at 252°C) by a 2 M CaCl₂-MgCl₂ aqueous solution are reported and discussed. Dolomitization of calcite proceeds via an intermediate high (ca. 35 mole %) magnesian calcite, whereas that of aragonite is carried out through the conversion of the reactant into a low (5.6 mole %) magnesian calcite which in turn transforms into a high (39.6 mole %) magnesian calcite. Both the intermediate phases and dolomite crystallize through a dissolution-precipitation reaction. The intermediate phases form under local equilibrium within a reaction zone surrounding the dissolving reactant grains. The volume of the reaction zone solution can be estimated from Sr²⁺ and Mg²⁺ partitioning equations. In the case of low magnesian calcite growing at the expense of aragonite at 252°C, the total volume of these zones is in the range of 2 × 10^?5 to 2 × 10^?4 1., out of 5 × 10^?3 1., the volume of the bulk solution.The apparent activation energies for the initial crystallization of high magnesian calcite and dolomite are 48 and 49 kcal/mole, respectively.Calcite transforms completely into dolomite within 100 hr at 252°C. The overall reaction time is reduced to approximately 4 hr at 295°C. The transformation of aragonite to dolomite at 252°C occurs within 24 hr. The nature of the reactant dictates the relative rates of crystallization of the intermediate phases and dolomite. With calcite as reactant, dolomite growth is faster than that of magnesian calcite; this situation is reversed when aragonite is dolomitized.Coprecipitation of Sr²⁺ with dolomite is independent of temperature (within analytical error) between 252 and 295°C. Its partitioning, with respect to calcium, between dolomite and solution results in distribution coefficients in the range of 2.31 × 10^?2 to 2.78 × 10^?2.     

Diagenetic model of carbonate rocks of Guri Member of Mishan Formation (Lower to Middle Miocene) SE Zagros basin,Iran

In order to understand the post-depositional history of carbonate rocks of Guri Member (Lower to Middle Miocene), three stratigraphic sections were selected in north Bandar-Abbas in southeast of Iran. Sampling was carried out, analyzed for selective parameters such as oxygen and carbon isotopic compositions (δ¹⁸O and δ¹³C) and interpreted in the present study. We recognized several diagenetic processes including micritization, cementation, neomorphism, compaction, dissolution, silicification, dolomitization, fracturing and vein filling. Some of the diagenetic processes occurred at different conditions, so in order to achieve precise interpretation, samples from different carbonate components such as, micrite, fracture cement, solution pore cement, intergranular cement, and some biotic allochems were analyzed. In this study micrite samples were subdivided into two groups including micro-spary and micrite. They were recognized under Cathodoluminescence microscope. In addition, micrite samples were classified into five groups based on their depositional environments: supratidal, lagoon, coral bar, open sea, and open basin. There were minor changes in stable isotope ratios based on the sedimentary environments, stratigraphy successions, and micro-spary or micrite properties. In this study, similar calcite cements in petrography studies were differentiated by stable isotope data. Those calcite cements have formed in different diagenetic environments such as meteoric and burial cements. Paragenetic sequence of carbonate rocks were interpreted by integration of petrographic and isotopic studies. We have reconstructed diagenetic models of Guri Member into four stages including marine, meteoric, burial, and uplifting.     

Dolomitization of Quaternary reef limestone, Aitutaki, Cook Islands

Six holes were drilled to depths of 30–69 m in the shallow lagoon of Aitutaki in the southern Cook Islands. One hole encountered pervasively dolomitized reef limestones at 36 m subbottom depth, which extended to the base of the drilled section at 69·3 m. This hole was drilled near the inner edge of the present barrier reef flat on the flank of a seismically defined subsurface ridge. Both the morphology and biofacies indicate that this ridge may represent an outer reef crest. Mineralogy, porosity and cementation change in concert downhole through three zones. Zone 1, 0–9 m, is composed of primary skeletal aragonite and calcite with minor void-filling aragonite and magnesian calcite cement of marine phreatic origin. Zone 2, 9–36 m, is composed of replacement calcite and calcite cement infilling intergranular, intragranular, mouldic and vuggy porosity. Stable isotopes (mean δ¹⁸O=—5·4‰ PDB for carbonate; δD =—50‰ SMOW for fluid inclusions) support the petrographic evidence indicating that sparry calcite cements formed in predominantly freshwater. Carbon isotope values of —4·0 to —11·0‰ for calcite indicate that organic matter and seawater were the sources of carbon. Zone 3, 36–69·3 m, is composed of replacement dolostone, consisting of protodolomite with, on average, 7 mol% excess CaCO₃ and broad and weak ordering X-ray reflections at 2·41 and 2·54 A. The fine-scale replacement of skeletal grains and freshwater void-filling cements by dolomite did not significantly reduce porosity. Stable isotopes (mean δ¹⁸O=+2·6‰₀ PDB for dolomite; maximum δD =—27‰ SMOW for fluid inclusions) and chemical composition indicate that the dolomite probably formed from seawater, although formation in the lower part of a mixed freshwater-seawater zone, with up to 40% freshwater contribution, cannot be completely ruled out. The carbon (δ¹³C=2·7‰) and magnesium were derived from seawater. Low-temperature hydrothermal iron hydroxides and associated transition metals occur in void space in several narrow stratigraphic intervals in the limestone section that was replaced by dolomite. The entire section of dolomite is also enriched in these transition metals. The metals dispersed throughout the dolostone section were introduced at the time of dolomitization by a different and later episode of hydrothermal circulation than the one(s) that produced the localized deposits near the base of the section. The primary reef framework is considered to have been deposited during several highstands of sea level. Following partial to local recrystallization of the limestone, a single episode of dolomitization occurred. Both tidal and thermal pumping drove large quantities of seawater through the porous rocks and perhaps maintained a wide mixing zone. However, the isotopic, geochemical and petrographic data do not clearly indicate the extent of seawater mixing.     

Shallow subsurface diagenesis of Pleistocene periplatform ooze: northern Bahamas

Previous studies on early submarine diagenesis of periplatform carbonates have implied that these originally polymineralic (aragonite, magnesian calcite, calcite) sediments are susceptible to early diagenesis only in current-swept open seaways or where surficially exposed by erosion on the seafloor. It has also been proposed that while in the shallow subsurface, periplatform oozes retain their original mineralogy for at least 200,000–400,000 yr and remain unlithified for tens of millions of years. Evidence is reported here for extensive calcitization and selective lithification of periplatform oozes of late Pleistocene age in two piston cores collected from water depths of ～ 1,000 m north of Little Bahama Bank. It is shown that shallow (<30 m) subsurface diagenesis can significantly alter the original mineralogy of periplatform oozes to predominantly calcite in less than 440,000 yr, and that cementation by calcite can produce chalk-ooze sequences within the same time-frame. Periplatform oozes that originally contain a high percentage of bank-derived magnesian calcite appear to have a higher diagenetic potential than those originally low in magnesian calcite. Shallow subsurface calcitization and fithification greatly reduce the diagenetic potential of periplatform carbonates, and chalk-ooze sequences apparently can persist for tens of millions of years and to burial depths of at least 300 m. Shallow subsurface diagenesis, at water depths > 1,000 m, proceeds via dissolution of magnesian calcite and aragonite and reprecipitation of calcite as allochem fillings, exterior overgrowths and cement. It is speculated that density-driven ‘Kohout convection‘, where seawaters under-saturated with respect to magnesian calcite and aragonite and saturated/supersaturated with respect to calcite flow through the margins of carbonate platforms, is the primary driving mechanism for shallow subsurface diagenesis. Removal of Mg during early stages of deep seafloor and shallow subsurface diagenesis should increase the Mg content of interstitial waters which is likely to increase the ‘dolomitizing potential’ of Kohout convection fluid flow.     

Low-magnesian calcite limestones forming at the deep-sea floor, Tongue of the Ocean, Bahamas

Carbonate ooze in the deep troughs between the Bahama Banks is a mixture of pelagic and bank-derived material. It consists of aragonite, calcite and magnesium calcite in a ratio of about 3:2:1. Where exposed in erosional cuts at the sea floor, this ooze lithifies within 100,000 years and is transformed into calcite micrite of only 3.5-5 mol % MgCO₃. Where buried, the ooze maintains its original composition for at least 200,000-400,000 years and remains unlithified for tens of millions of years. Quite unexpectedly, the path of sea-floor diagenesis of peri-platform ooze was found to be the same as that of freshwater diagenesis. Most of the aragonite is leached, pteropod shells often leaving cement-lined moulds behind; magnesian calcite recrystallizes and loses magnesium; polyhedral calcite of 2-4 μm size appears as cement. The setting and the carbon-oxygen isotope ratios rule out any freshwater influence. Carbon isotope ratios remain heavy, oxygen ratios shift towards equilibrium with the cold bottom water. The calcite cement has 3.5-5 mol % MgCO₃ and can be interpreted as the least soluble form of calcite emerging from alteration at the sea floor or, alternatively, as a direct precipitate from cold sea water. The change in the composition of calcite cements with water depth supports the second interpretation. In the Bahamas and elsewhere in the world ocean, magnesium in calcite cements decreases from the warm surface waters down to 700-1200 m, i.e. the boundary between intermediate and cold deep-water masses. Below this level, calcite prevails and magnesian calcite and aragonite cements are restricted to semi-enclosed seas with exceptionally warm bottom waters.     

Disseminated ‘jigsaw piece’ dolomite in Upper Jurassic shelf sandstones,Central North Sea: an example of cement growth during bioturbation?

Unusual textural and chemical characteristics of disseminated dolomite in Upper Jurassic shelf sediments of the North Sea have provided the basis for a proposed new interpretation of early diagenetic dolomite authigenesis in highly bioturbated marine sandstones. The dolomite is present throughout the Franklin Sandstone Formation of the Franklin and Elgin Fields as discrete, non‐ferroan, generally unzoned, subhedral to highly anhedral ‘jigsaw piece’ crystals. These are of a similar size to the detrital silicate grains and typically account for ≈5% of the rock volume. The dolomite crystals are never seen to form polycrystalline aggregates or concretions, or ever to envelop the adjacent silicate grains. They are uniformly dispersed throughout the sandstones, irrespective of detrital grain size or clay content. Dolomite authigenesis predated all the other significant diagenetic events visible in thin section. The dolomite is overgrown by late diagenetic ankerite, and bulk samples display stable isotope compositions that lie on a mixing trend between these components. Extrapolation of this trend suggests that the dolomite has near‐marine δ¹⁸O values and low, positive δ¹³C values. The unusual textural and chemical characteristics of this dolomite can all be reconciled if it formed in the near‐surface zone of active bioturbation. Sea water provided a plentiful reservoir of Mg and a pore fluid of regionally consistent δ¹⁸O. Labile bioclastic debris (e.g. aragonite, Mg‐calcite) supplied isotopically positive carbon to the pore fluids during shallow‐burial dissolution. Such dissolution took place in response to the ambient ‘calcite sea’ conditions, but may have been catalysed by organic matter oxidation reactions. Bioturbation not only ensured that the dissolving carbonate was dispersed throughout the sandstones, but also prohibited coalescence of the dolomite crystals and consequent cementation of the grain framework. Continued exchange of Mg²⁺ and Ca²⁺ with the sea‐water reservoir maintained a sufficient Mg/Ca ratio for dolomite (rather than calcite) to form. Irregular crystal shapes resulted from dissolution, of both the dolomite and the enclosed fine calcitic shell debris, before ankerite precipitation during deep‐burial diagenesis.     

Dolomite textures in the Upper Cretaceous carbonate-hosted Pb–Zn deposits,Zakho, Northern Iraq

In the northeast of Zakho City, Northern Iraq, the host rocks of Pb–Zn deposits are composed predominantly of dolomites with subordinate dolomitic limestone intervals. This study is focused on the dolomites of the Bekhme Formation (Upper Campanian) carbonate-hosted Pb–Zn deposits. The amount of dolomites, however, increases toward the mineralized zone. Dolomites are dominated by replacement dolomite with minor dolomite cements. Petrography study allowed identification of six different dolomite textures. These are (1) fine crystalline, planar-s (subhedral) dolomite, RD1; (2) medium to coarse crystalline, planar-e (euhedral) to planar-s (subhedral) dolomites, RD2; (3) medium crystalline, planar-s (subhedral) to nonplanar-a (anhedral) dolomites, RD3; (4) coarse crystalline, planar-s (subhedral) to nonplanar-a (anhedral) dolomites, RD4; (5) planar (subhedral) void-filling dolomite cements, CD1; and (6) nonplanar (saddle) void-filling dolomite, CD2. The RD1, RD2, RD3, and RD4 dolomite textures are replacive in origin and are volumetrically the most important types, whereas CD1 and CD2 dolomites with sparry calcite are commonly cements that fill the open spaces. Although the dolomites of the Bekhme Formation are not macroscopically observed in the field, their different types are easily distinguished by petrographic examination and scanning electron microscopy. It was observed that the dolomites of the Bekhme Formation are formed in two different diagenetic stages: the early diagenetic from mixing zone fluids at the tidal–subtidal (reef) environments and the late diagenetic from basinal brines which partially mixed with hydrothermal fluids at the shallow-deep burial depths. The latter occurs often with sphalerite, galena, and pyrite within mineralized zone. These dolomite types are associated base-metal mineralization (Mississippi Valley type).     

Holocene carbonate sedimentation in Lake Manitoba, Canada

The carbonate mineral suite of the modern offshore bottom sediment of the South Basin of Lake Manitoba consists mainly of high magnesian calcite and dolomite with minor amounts of low-Mg calcite and aragonite. The high-Mg calcite is derived from inorganic precipitation within the water column in response to supersaturation brought about by high levels of organic productivity in the basin. Both dolomite and pure calcite are detrital in origin, derived from erosion of the surrounding carbonate-rich glacial deposits. Aragonite, present only in trace amounts in the offshore sediments, is bioclastic in origin. The upward increase in the amount of magnesian calcite in the post-glacial sediment record is attributed to increasing photosynthetic utilization of CO₂ in the lake. Stratigraphic variation in the amount of magnesium incorporated into the calcite lattice is interpreted as reflecting a variable magnesium input to the lake from ground water and surface runoff, and possibly variable calcium removal in the precipitating lake water. The effects of long-term chemical weathering at the source and size segregation explain the changes in dolomite content throughout the section.     

Cathodoluminescent bimineralic ooids from the Pleistocene of the Florida continental shelf

A bored and encrusted late Pleistocene ooid grainstone was recovered from the seafloor at a depth of approximately 40 m on the outer continental shelf of eastern Florida. Ooid cortices are dominantly bimineralic, generally consisting of inner layers of radial magnesian calcite and outer layers of tangential aragonite. Ooid nuclei are dominantly rounded cryptocrystalline grains, although quartz grains and a variety of skeletal grains also occur as nuclei. Ooids are partially cemented by blocky calcite, and interparticle porosity is partially filled by micrite. Radial cortex layers are composed of brightly cathodoluminescent magnesian calcite having a composition of approximately 12 mol% MgCO₃ and 1000 ppm strontium. The iron and manganese concentrations in radial cortex layers are generally in the range of 500–1000 ppm and 100–250 ppm, respectively. Tangential cortex layers are composed of noncathodoluminescent aragonite containing approximately 11 500 ppm strontium and less than 0.5 mol% MgCO₃. Iron concentrations in tangential cortex layers are generally in the range of 150–400 ppm, and manganese concentrations are generally below the detection limit of 100 ppm. Echinoderm skeletal fragments, which are present as accessory grains, are composed of brightly cathodoluminescent magnesian calcite. Some ooid nuclei and the thin outer edges of some blocky calcite cement are cathodoluminescent; micrite matrix and the bulk of blocky calcite cement are noncathodoluminescent. Ooids do not exhibit textural evidence of recrystallization. The ooid grainstone underwent an episode of meteoric diagenesis. but ooid cortices were not affected by the event. We propose a previously unrecognized process by which the magnesian calcite cortex layers underwent diagenetic alteration in oxygen-depleted seawater. During this diagenesis, magnesium was lost and manganese was incorporated without apparent textural alteration and without mineralogical stabilization. Thus, we Suggest that cathodoluminescence may result from diagenetic alteration on the sea-floor.     

华南地区二叠纪栖霞组燧石结核成因研究及其地质意义

燧石结核是华南地区二叠纪栖霞组的重要识别特征之一，其成因具重要的古地理、古海洋意义。通过对湖北黄石、江苏南京和广西来宾三地栖霞组燧石结核的岩石矿物学研究，确定了栖霞组燧石结核的矿物组成和成岩作用序列。研究区燧石结核主要由微石英、负延性玉髓、粗晶石英组成，并含少量白云石、方解石及生物碎屑。其中，微石英、负延性玉髓、正延性玉髓、白云石形成于早期成岩作用，方解石晶粒形成于晚期成岩作用，粗晶石英的形成则具有多期性。结合栖霞组菊花状天青石和海泡石成因研究结果，本文认为组成栖霞组燧石结核的硅质来源与当时全球硅质生物的繁盛有关。燧石结核内玉髓和白云石形成环境条件及形成时间的确定，为建立更加合理的燧石结核成因模式和白云岩化模式提供了重要资料，同时也对深入探讨本区二叠纪层状硅质岩的成因具启发意义。     

川西南中二叠统中粗晶白云石流体来源分析

四川盆地西南地区中二叠统地层在埋藏过程中发生了较高程度的白云岩化。通过野外剖面观察和详细的薄片岩石学研究,在中二叠统白云岩储层中识别出了四种类型的白云石（包括三种基质交代白云石和一种白云石胶结物）:1）粉晶白云石,宏观上主要呈层状发育,晶粒小于50 μm,平直镜面半自形晶-非平直晶面它形晶;2）细晶白云石,晶粒大小为50~250 μm,平直晶面半自形晶-自形晶;3）中粗晶白云石,宏观上可见溶蚀孔洞和裂缝发育,其中充填白色的白云石胶结物、方解石胶结物等,晶粒大小为250 μm~2 mm,非平直晶面它形晶;4）白云石胶结物,以胶结物的形式在裂缝和溶蚀孔洞中发育,晶粒大小变化较大,具有明显的波状消光。利用不同矿物之间的接触和切割关系,结合阴极发光和扫描电镜等手段,确定了几种白云石和相关成岩矿物的形成时序,确立四川盆地西南地区中二叠统白云岩的成岩演化序列。即从成岩早期到晚期,依次形成（或发生成岩作用）了粉晶白云石、早期溶蚀作用、细晶白云石、中粗晶白云石、水力压裂缝、白云石胶结物、石英、方解石脉、缝合线、晚期溶蚀和沥青充填。通过地球化学和包裹体分析,发现中粗晶白云石和白云石胶结物具有相似的地球化学特征,即明显偏负的氧同位素、大于同期海水的Sr同位素,成岩流体具有较高的温度和盐度,表明其成岩流体具有典型的热液性质。原始灰岩和早期白云岩经热液改造,重结晶为中粗晶白云石,并在裂缝和溶蚀孔洞中沉淀鞍形白云石胶结物。     

震旦纪灯影组磷块岩及其生成特点

灯影组磷块岩有四种类型,即泥晶磷块岩、内碎屑磷块岩、藻磷块岩和细晶磷块岩。组成磷块岩的主要矿物是磷灰石、白云石、石英和少量伊利石等。磷块岩主要沉积在陆缘海内,它的沉积环境是与深水有联系的浅水地区。深水和浅水环境的地质背景分别为构造拗陷和碳酸盐岩台地。前者提供成矿物质,后者提供有利于磷质成矿的沉积环境。     

Dolomite-calcite textures in early carbonatites of the Kovdor ore deposit,Kola peninsula,Russia: their genesis and application for calcite-dolomite geothermometry

In early calcite carbonatites of the Kovdor ore deposit four morphological types of dolomite are represented. In the first type, dolomite microcrystals occur as lamellae enclosed by optically continuous calcite. In the second, dolomite microcrystals occur as segmented rods, plates and xenomorphic grains, enclosed by optically discontinuous calcite, and in the third, dolomite is represented by grains of various morphologies, situated along calcite grain boundaries. The fourth type of dolomite occurs as a fine-grained aggregate, which develops along grain boundaries and cleavage cracks of calcite. From microscopic, scanning electron microscope and microprobe studies of these different types of dolomite microcrystals, as well as the calcite associated with them, it can be concluded that the first type of dolomite was exsolved from magnesian calcite during cooling. The second, and the third types of dolomite microcrystals were formed by recrystallization. The fourth type of dolomite was formed by metasomatic dolomitization. As the result of these two processes-recrystallization and metasomatic dolomitization-early dolomite microcrystals seldom occur. The composition of the early-formed primary magnesian calcite yielded temperatures of exsolution of dolomite from magnesian calcite between 665 and 700°C.     

The Mineral Geochemical Discrimination of the Calcite Crystals in the Pores of Upper Ordovician Limestone and Its Environmental Significance: Take Tazhong Oilfield of Tarim Basin for Example

Based on the analysis of the morphology, order, cathodoluminescence and microelement of the calcite crystals in the pores of Upper Ordovician limestone in Tazhong oilfield of Tarim Basin, this paper suggest that the calcite crystals can divided 11 kinds of cements into three stages, and confirms their cementation sequence characteristics and formation environment. First stage of the cementation occurred on the bottom of the diagenetic environment, the product of which mainly are microcrystalline, fine shape, radiation fibrous, fasciculation, radiation axis shape calcites and a ball-like aragonite, whose filling pore is 0%–30%; the second one occurred in the atmospheric fresh water environment, with main cement types of crescent or pendulous shape, vadose silt, hyperplasia of coaxial, the filling pore of which is 5%–100%; the third one occurred in a burial environment, the crystals of which are bright and thick, mainly coarse sparry and poikilitic calcite, with filling pore of 5%–5%. In this paper, influence from each stage of cementation on porosity is analyzed, and pore evolution is established.     

一种严格受控于环境和时间的特殊碳酸盐岩——臼齿构造碳酸盐岩

臼齿构造碳酸盐岩是一种具有类似于大象臼齿特征的特殊碳酸盐岩，其微亮晶脉由纯净的、基本等粒的方解石（或白云岩）构成，而基质物质则由细粒的、富泥质的灰岩组成。通过对中朝板块东部吉辽徐淮地区前寒武纪臼齿构造碳酸盐岩研究，结合国外研究资料，臼齿构造碳酸盐岩具有特定的生存时限，目前只在前寒武纪（主要发育在中、新元古代）地层中发现。研究表明，臼齿构造碳酸盐岩发育在缓坡型台地，宿主岩性以富含泥质的粉屑灰岩、泥晶灰岩为主，位于潮汐流、风暴流影响范围内，为浅潮下和环潮坪环境，潮上带与深缓坡均不发育，具有鲜明的环境和相指示意义。由于缺乏现代相似沉积物，臼齿构造碳酸盐岩的成因还是一个谜，需要进一步研究和探索。 