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1.
Comparison of Upper Guadalupian fore-reef, reef and back-reef strata from outcrops in the Guadalupe Mountains with equivalent subsurface cores from the northern and eastern margins of the Delaware Basin indicates that extensive evaporite diagenesis has occurred in both areas. In both surface and subsurface sections, the original sediments were extensively dolomitized and most primary and secondary porosity was filled with anhydrite. These evaporites were emplaced by reflux of evaporitic fluids from shelf settings through solution-enlarged fractures and karstic sink holes into the underlying strata. Outcrop areas today, however, contain no preserved evaporites in reef and fore-reef sections and only partial remnants of evaporites are retained in back-reef settings. In their place, these rocks contain minor silica, very large volumes of coarse sparry calcite and some secondary porosity. The replacement minerals locally form pseudomorphs of their evaporite precursors and, less commonly, contain solid anhydrite inclusions. Some silicification, dissolution of anhydrite and conversion of anhydrite to gypsum have occurred in these strata where they are still buried at depths in excess of 1 km; however, no calcite replacements were noted from any subsurface core samples. Subsurface alteration has also led to the widespread, late-stage development of large- and small-scale dissolution breccias. The restriction of calcite cements to very near-surface sections, petrographic evidence that the calcites post-date hydrocarbon emplacement, and the highly variable but generally ‘light’carbon and oxygen isotopic signatures of the spars all indicate that calcite precipitation is a very late diagenetic (telogenetic) phenomenon. Evaporite dissolution and calcitization reactions have only taken place where Permian strata were flushed with meteoric fluids as a consequence of Tertiary uplift, tilting and breaching of regional hydrological seals. A typical sequence of alteration involves initial corrosion of anhydrite, one or more stages of hydration/dehydration during conversion to gypsum, dissolution of gypsum and precipitation of sparry calcite. Such evaporite dissolution and replacement processes are probably continuing today in near-outcrop as well as deeper settings. This study emphasizes the potential importance of telogenetic processes in evaporite diagenesis and in the precipitation of carbonate cements. The extensive mineralogical and petrophysical transformations which these strata have undergone during their uplift indicates that considerable caution must be exercised in using surface exposures to interpret subsurface reservoir parameters in evaporitic carbonate rocks.  相似文献   

2.
This study reports a complex fluid and thermal history using petrography, electron microprobe, isotopic analysis and fluid inclusions in replacement minerals within gypsum pseudomorphs in Tithonian-Berriasian lacustrine deposits in Northern Spain. Limestones and dolostones, formed in the alkaline lakes, contain lenticularly shaped gypsum pseudomorphs, considered to form in an evaporative lake. The gypsum was replaced by quartz and non-ferroan calcite (Ca-2), which partially replaces the quartz. Quartz contains solid inclusions of a preexisting non-ferroan calcite (Ca-1), anhydrite and celestine. High homogenization temperatures (T h ) values and inconsistent thermometric behaviour within secondary fluid inclusion assemblages in quartz (147?C351°C) and calcite (108?C352°C) indicate high temperatures after precipitation and entrapment of lower temperature FIAs. Th are in the same range as other reequilibrated fluid inclusions from quartz veins in the same area that are related to Cretaceous hydrothermalism. Gypsum was replaced by anhydrite, likely during early burial. Later, anhydrite was partially replaced by Ca-1 associated with intermediate burial temperatures. Afterward, both anhydrite and Ca-1 were partially replaced by quartz and this by Ca-2. All were affected during higher temperature hydrothermalism and a CO2-H2O fluid. Progressive heating and hydrothermal pulses, involving a CO2-H2O fluid, produce the reequilibration of the FIAs, which was followed by uplift and cooling.  相似文献   

3.
Lithologic succession, microscopic examination as well as X-ray diffraction and chemical data revealed that the surface Middle Miocene evaporites of Wadi Quei are composed of anhydrite beds intercalated with carbonate and green shale, whilst the subsurface evaporites of Gemsa locality are composed of gypsum, anhydrite, carbonates and celestite with a rare amount of halite. The anhydrite is found to be formed diagenetically after gypsum. The carbonate is interpreted as having been of biogenic origin. The strong smell of H2S and golden crystals of pyrite at Wadi Quei beds are indications of the biogenic action of sulphate-reducing bacteria in the presence of organic matter. It is suggested that the evaporite sequence which was deposited in a supratidal sabkha environment is characterized by alkaline-reducing conditions. The presence of nodular gypsum at Gemsa locality is probably deposited in a supratidal environment with oscillation of sea level.  相似文献   

4.
Gold nuggets (centimetre scale) have formed in a supergene alteration zone on hydrothermal gold deposits, and occur intergrown with quartz and iron oxyhydroxide pseudomorphs after sulphide minerals, and along fractures in quartz and host rocks. The supergene alteration was driven by groundwater-driven water-rock interaction near to a regional unconformity beneath fluvial sediments, and involved clay alteration and oxidation that extended up to 50 m below the unconformity. Oxidation of pyrite and arsenopyrite produced temporary thiosulphate ligands that mobilised microparticulate gold encapsulated in the sulphide minerals. The nuggets have some crystalline form, and internally they consist of anhedral grains, elongated gold plates, and intimate intergrowths of gold and iron oxyhydroxide. Nugget surfaces have further micron scale overgrowths of microparticulate gold, gold plates, and gold crystals. Nuggets were eroded and recycled into nearby proximal Miocene quartz pebble conglomerates, where they concentrated in placers near the basal unconformity. Later recycling transferred gold into Pleistocene fluvial channels. Gold dissolution and redeposition as plates and crystals occurred on the exterior surfaces of placer gold particles, with little change in mass. All groundwater maintained high pH throughout the geological history because there was sufficient calcite in the basement rocks to neutralise any acid generated by pyrite oxidation. Hence, gold mobility in sediments was driven by thiosulphate complexes as for the in situ nuggets, albeit with lower dissolved sulphur concentrations. Despite aridification of the climate in the late Cenozoic, with resulting localised high dissolved chloride concentrations, chloride complexation did not contribute to gold mobility.  相似文献   

5.
The Lower Werra Anhydrite (Zechstein, Upper Permian) deposits of the teba area originated in a deep basin setting, in shallow to deep water conditions. Facies changes occur within small distances and suggest fluctuating boundaries between well defined basins and platforms. This pattern of local platforms and adjacent basins developed during deposition. In basinal areas, the sequence is clearly transgressive, whereas on platforms accumulation kept pace with subsidence after an initial transgression. Nodular anhydrite represents a polygenetic deposit which formed at different times with respect to deposition. Massive anhydrite with pseudomorphs after upright-growth gypsum crystals suggest rapid precipitation in a subaqueous environment and/or fluctuating, but generally high, salinity conditions. Massive clastic sulphate originated due to periodic high energy events and resedimentation, or due to brecciation possibly connected with salinity fluctuations and the dissolution of halite. Massive, textureless anhydrite is locally porous and passes upward into breccia, indicating a strongly saline environment. Bedded anhydrite is considered to form in shallow water environments and laminated anhydrite in deep water. Bedded anhydrites contain portions which are graded. Intercalations of sulphate turbidites and upright-growth gypsum suggest fluctuating water depths, with comparatively deep water during turbidite deposition, but shallower conditions during upright-growth gypsum deposition. The sequence observed in slope zones at platform-basin margins, detrital (parautochthonous) sulphate sand to graded beds to basinal laminites, indicates that redistribution processes were important. At the onset of the Lower Werra Anhydrite deposition bathymetric relief existed between the central part of the basin and its margins, where carbonate platforms remained subaerially exposed. Formation of local platforms and adjacent basins required a relatively high subsidence rate, as pre-existing relief cannot account for the total accumulated thickness of the Lower Werra Anhydrite deposits. One implication of this is that the main argument against ‘the shallow water - shallow basin’ evaporite basin model, i.e.,a very fast rate of subsidence, may not be valid for the Łeba Lower Werra Anhydrite basin.  相似文献   

6.
The Badenian (Middle Miocene) Ca-sulphate deposits of the fore-Carpathian basin – including the shelf and adjacent salt depocentre – have undergone varying degrees of diagenetic change: they are preserved mainly as primary gypsum in the peripheral part of the platform, whereas toward the centre of the basin, where great subsidence occurred during the Miocene, they have been totally transformed into anhydrite. The facies variation and sequence of Badenian anhydrites reflect different genetic patterns of two members of the Ca-sulphate formation. In the lower member (restricted to the platform), anhydrite formed mainly by synsedimentary anhydritization (via nodule formation), whereas in the upper member (distributed throughout the platform and depocentre) the various gypsum/anhydrite lithofacies display a continuum of distinctive anhydrite type-fabrics. These fabrics are based on petrographic features and show from the centre to the margin: (1) syndepositional, interstitial growth of displacive anhydrite; (2) early diagenetic, displacive to replacive (by replacement of former gypsum) anhydrite formation near the depositional surface; (3) early diagenetic, displacive to replacive anhydrite formation during shallow burial; and (4) late-diagenetic (and only partial) replacement of gypsum at deeper burial. The cross-shelf lateral relations of anhydrite lithofacies and fabrics suggest that the diagenesis developed as a diachronous process. These fabrics of the upper member reflect both palaeogeographic (linked to different parts of the basin) and burial controls. Anhydrite growth started very early in the basin centre, presumably related to high-salinity pore fluids; anhydritization prograded updip toward the shelf (landward in a generalized cross-section through the basin). The intensity of gypsum replacement by anhydrite was progressively attenuated landward by a decrease in the salinity of the pore fluids. In each part of the basin, the anhydrite fabric was also controlled by the texture and degree of lithification of the fine-grained primary gypsum lithofacies. Recrystallization of these anhydrite fabrics during late diagenesis, linked to deeper burial conditions, is insignificant, allowing reconstruction of the original anhydritization pattern.  相似文献   

7.
PERYT  PIERRE  & GRYNIV 《Sedimentology》1998,45(3):565-578
Polyhalite deposits in the Zechstein (Upper Permian) of northern Poland occur in the Lower Werra Anhydrite. In the Zdrada Sulphate Platform, the polyhalite appears to be a very early replacement of anhydrite. The replacement was caused by the halite-precipitating brines which contained potassium and magnesium ions. The formation of polyhalite was preceded by the syndepositional anhydritization of the original gypsum deposit which has often preserved its primary textures. This anhydritization on the platform and its slopes was a reaction of the precipitated gypsum in a hydrologically open evaporite basin, with brines of salt basins adjacent to the sulphate platform. These brines, when nearly saturated with respect to halite, and potassium and magnesium rich, reacted with anhydrite to precipitate polyhalite along the slopes of the Zdrada Platform. The oxygen and sulphur isotopic compositions of sulphate evaporites indicate that marine solutions were the only source of sulphate ions supplied to the Zechstein basin, and that anhydrite was transformed to polyhalite by reaction with marine brines more concentrated than those that precipitated precursor calcium sulphate minerals.  相似文献   

8.
This paper describes and interprets the mineral and facies assemblages that occur in carbonate–evaporite shallow lacustrine deposits, considering the importance of the processes pathway (i.e. dolomitization, gypsum calcitization and silicification). The Palaeogene deposits of the Deza Formation (Almazán Basin, central‐northern Spain) are selected as a case study to determine the variety of physicochemical processes taking place in carbonate–evaporite shallow lakes and their resulting diagenetic features. Dolostones are the predominant lithology and are composed mainly of dolomite with variable amounts of secondary calcite (5 to 50%), which mainly mimic lenticular gypsum (pseudomorphs). Five morphological types of dolomite crystal were identified as follows: dolomite tubes, dolomite cylinders, rhombohedral dolomite, spheroidal and quasi‐rhombohedral dolomite, and cocoon‐shaped dolomite. The dolomite cylinders and tubes are interpreted as the dolomitized cells of a widespread microbial community. The sequence of diagenetic processes started with growth of microlenticular interstitial gypsum in a calcareous mud deposited on the playa margin mudflats, and that sometimes included microbial sediments. Immediately following growth of gypsum, dolomite replaced the original calcite (or possibly aragonite) muds, the microbial community and the gypsum. Partial or total replacement of gypsum by dolomite was related mainly to the biomineralization of endolithic microbial communities on gypsum crystals. Later calcitization took place under vadose, subaerial exposure conditions. The development of calcrete in distal alluvial settings favoured the release of silica and subsequent silicification on the playa margin mudflats. Stable isotope compositions of calcite range from ?9·02 to ?5·83‰ δ13CPDB and ?7·10 to 1·22‰ δ18OPDB; for the dolomite, these values vary from ?8·93 to ?3·96‰ δ13CPDB and ?5·53 to 2·4‰ δ18OPDB. Quartz from the cherts has δ18OSMOW values ranging from 27·1 to 31·1‰. Wide variation and relatively high δ18OSMOW values for dolomite indicate evaporitic and closed hydrological conditions; increased influx of meteoric waters reigned during the formation of secondary calcite spar.  相似文献   

9.
ABSTRACT The Tripoli Formation (Lower Messinian) in Sicily includes diatomites irregularly alternating with marl and carbonate beds and lies, stratigraphically, between the Tortonian pelagic marls and the evaporitic Calcare di base. The relationships between mineralogy, textural features and oxygen-carbon isotopic compositions of carbonate components point to a wide variability of depositional conditions and suggest that Tripoli sedimentation occurred in small basins characterized by periodic and marked restriction from the open sea.
The isotopic values of calcite and dolomite in the diatomites suggest an evolution from normal marine towards more restricted environments. Evaporating conditions are also indicated by the occurrence of anhydrite, length-slow chalcedonic quartz and moulds of gypsum. In a more advanced stage, the precipitation of heavy δ180 dolomite in the interstitial pores of fossil-poor diatomites denotes an environment with highly evaporated water. Mixing of meteoric and marine waters, on the other hand, might have favoured the precipitation of a dolomite characterized by relatively low δ180 and δ13C values.
The deposition of marl and carbonate beds alternating with or overlying the diatomites took place in an environment with highly evaporated marine waters on the basis of δl18O values of dolomite (up to + 9.10‰) and aragonite (up to + 5.83‰), occurrence of evaporitic minerals and lack of fossils. The presence at these levels of calcite with extremely negative δ13C values (down to - 38.40‰), filling gypsum moulds, suggests activity of sulphate-reducing bacteria. Some aragonitic marls, however, bear evidence of deposition in relatively normal marine conditions.  相似文献   

10.
Experimental partioning of Sr between solutions, aragonite, calcite, gypsum and anhydrite show that the isomorphous replacement of Ca2+ by Sr2+ can be described as a linear function. The constants of the distributions are used to calculate primary Sr-contents of the various Ca-carbonates and Ca-sulfates precipitated from seawater and to estimate the point of precipitation of celestite. Comparism of these data with actual Sr-contents in sediments and sedimentary rocks show that in most cases gypsum has to be considered as the primary precipitate. Anhydrite in general is formed by diagenetic alteration of gypsum. The average Sr-content of gypsum rocks make it very probable that the Sr-concentration of seawater has stayed virtually unchanged since the end of Mesozoic. Sr-contents of carbonate rocks show that most of the limestones have been altered diagenetically. The distribution of Sr within the various sedimentary units of the earth's crust make it very probable that this alteration occurred in a system open to pore solutions.  相似文献   

11.
四川渠县三叠系膏盐的同生、成岩、后生及表生变化   总被引：1，自引：0，他引：1  
隗合明 《沉积学报》1987,5(4):56-65
本文论述了四川渠县三叠系的膏盐在沉积后的不同阶段所发生的各种变化,并提出根据膏盐的变化特征推测它们的原生沉积条件、卤水咸化程度及研究区的矿床保存条件。  相似文献   

12.
The Abu Ruweis Formation is composed of carbonates, evaporites, and mudstones, with some locally developed pelletic, oolitic and stromatolitic limestones. The lateral persistence of bedding, the purity of the evaporite rocks, the alternating arrangement of marine carbonates and evaporites indicates periodic deposition in subaqueous conditions (salina). Petrographic investigations, X-ray diffraction analysis as well as chemical analysis have shown that the outcropping evaporite beds are mainly composed of secondary gypsum, with rare anhydrite relics. Five microfacies of gypsum were recognized according to their fabrics: porphyroblastic and granoblastic gypsum showing polarization texture, gypsum pseudomorph after anhydrite laths, and satin spar gypsum. The textures they display indicate a hydration origin of precursor anhydrite, which is in turn rehydrated from primary gypsum. Some of these anhydrites were formed as a result of replacement processes of the carbonate sediments associated with the evaporites, as evidenced from the textural relationships of the carbonate and sulfate minerals. The O18 content ranges from 1.45 to 8.38% PDB and the C13 content ranges from −1.52 to 4.73% PDB. Trace elements analysis has shown that the Abu Ruweis dolomites are rich in strontium (up to 600 ppm), and sodium (up to 835 ppm). The isotope composition and trace elements content, as well as the petrographic characteristics point to a penecontemporaneous hypersaline dolomitization origin for the Abu Ruweis dolomites. The evaporites were deposited during a regressive lowstand systems tract, whereas the carbonates were deposited under shallow water marine conditions during a highstand systems tract. The Abu Ruweis succession represents a relatively stable arid climate within a rapidly subsiding basin. Restricted conditions were provided by the development of beach barriers.  相似文献   

13.
Samples of chert nodules, diagenetic carbonates and evaporites (gypsum/anhydrite) collected from the gypsiferous limestones of the Kef Eddour Member (Ypressian‐Priabonian) near Metlaoui and Sehib (Tunisia) show selective silicification with great variety in the silicified by‐products. Based on δ13C values, which support an organic origin for the carbon, carbonates replaced evaporites microbially through bacterial sulphate reduction. Observations and results suggest two scenarios for chert formation that are related to the rate and timing of diagenetic carbonate replacement of the evaporites (anhydrite/gypsum). In the absence of early diagenetic carbonate phases, silica with δ18O values from +25 to +28·6‰ [standard mean ocean water (SMOW)] replaced the outer parts of anhydrite nodules at pH < 9. In contrast, pore‐fluid pH values > 9 in the innermost parts of the anhydrite nodules prevented silica precipitation. The record of this chemical barrier is preserved in the microquartz rims and geode features that formed in the inner parts of the nodules after dissolution of the anhydrite nucleus. The microbial diagenetic replacement of evaporites (bacterial sulphate reduction) by carbonates (calcite, aragonite and dolomite) favoured silica replacement of carbonates rather than evaporites. Silica, with δ18O signature of +21 to +26‰ (SMOW), replaced carbonates on a volume‐for‐volume basis, yielding a more siliceous groundmass, and accounting for 90–95% of the nodules. The relatively higher δ18O values of quartz replacing anhydrite can be explained by a diagenetic fluid in equilibrium with mixed (meteoric/marine) to marine water. The lower δ18O values of the quartz that replaced the diagenetic carbonates are ascribed to flushing by meteoric water in a later diagenetic stage. The silica supply for chert formation could be derived from the reworked bio‐siliceous deposits (diatomites) to the west of the basin [vestiges of an opal‐CT precursor undetectable by X‐ray diffraction (XRD) were revealed by δ29Si magic‐angle‐spinning nuclear magnetic resonance investigations], diagenesis of the extraformational and overlying clay‐rich beds (the host limestones are clay‐poor as shown by XRD measurements), and minor volcanogenic and hydrothermal contributions during early diagenetic stages.  相似文献   

14.
安徽向山铁硫矿区硬石膏岩热水沉积特征及成因意义   总被引：2，自引：1，他引：1  
安徽向山地区铁、硫矿床中存在大片硬石膏岩 ,其Cu、Pb、Zn、As、Sb等元素含量都比较高 ,Sr元素含量在 0 .0 5 %～ 0 .6 0 %之间 ,且具有稀土总量低 ,铈、铕元素明显亏损等特征。据对其岩石学、岩石化学和硫同位素等特征综合研究表明 :矿床附近的硬石膏岩属热水成因 ,硫可能来源于下伏地层及深部。  相似文献   

15.
Fluid inclusion studies in combination with hydrogen, oxygen and sulphur isotope data provide novel insights into the genesis of giant amethyst-bearing geodes in Early Cretaceous Paraná continental flood basalts at Amestita do Sul, Brazil. Monophase liquid inclusions in colourless quartz, amethyst, calcite, barite and gypsum were analysed by microthermometry after stimulating bubble nucleation using single femtosecond laser pulses. The salinity of the fluid inclusions was determined from ice-melting temperatures and a combination of prograde and retrograde homogenisation temperatures via the density maximum of the aqueous solutions. Four mineralisation stages are distinguished. In stage I, celadonite, chalcedony and pyrite formed under reducing conditions in a thermally stable environment. Low δ34SV-CDT values of pyrite (?25 to ?32?‰) suggest biogenic sulphate reduction by organotrophic bacteria. During the subsequent stages II (amethyst, goethite and anhydrite), III (early subhedral calcite) and IV (barite, late subhedral calcite and gypsum), the oxidation state of the fluid changed towards more oxidising conditions and microbial sulphate reduction ceased. Three distinct modes of fluid salinities around 5.3, 3.4 and 0.3 wt% NaCl-equivalent characterise the mineralisation stages II, III and IV, respectively. The salinity of the stage I fluid is unknown due to lack of fluid inclusions. Variation in homogenisation temperatures and in δ18O values of amethyst show evidence of repeated pulses of ascending hydrothermal fluids of up to 80–90 °C infiltrating a basaltic host rock of less than 45 °C. Colourless quartz and amethyst formed at temperatures between 40 and 80 °C, while the different calcite generations and late gypsum precipitated at temperatures below 45 °C. Calculated oxygen isotope composition of the amethyst-precipitating fluid in combination with δD values of amethyst-hosted fluid inclusions (?59 to ?51?‰) show a significant 18O-shift from the meteoric water line. This 18O-shift, high salinities of the fluid inclusions with chloride-sulphate composition, and high δ34S values of anhydrite and barite (7.5 to 9.9?‰) suggest that sedimentary brines from deeper parts of the Guaraní aquifer system must have been responsible for the amethyst mineralisation.  相似文献   

16.
塔里木盆地塔中地区深埋碳酸盐岩储层显示出极强的非均质性。如灰岩地层孔隙度极低,而含酸性气藏的白云岩储层最大孔隙度高达27%。然而,造成这些现象的原因仍然不清楚。通过岩芯、薄片、扫描电镜观察,结合流体包裹体均一温度、盐度分析,方解石、白云石的碳氧同位素测定,试图解决这一问题。前人研究认为,塔中地区碳酸盐岩优质储层分布主要受控于原始沉积条件（如高能的礁滩相）和表生溶蚀,热液活动和断裂活动也起到重要作用。然而,多期流体活动和成岩作用导致大量同生期和表生期形成的溶蚀孔洞被破坏。在某些井区（如ZG9井和TZ75井）,埋藏溶蚀作用可能对优质储层形成起到重要作用。在寒武系和奥陶系岩芯中发现了大量硬石膏、重晶石、黄铁矿、沥青、方解石等,方解石交代硫酸盐,方解石具有较高的均一温度及较低的碳同位素值说明其形成与热化学硫酸盐还原作用（TSR）有关。在发生TSR的白云岩井段,储层物性较好,说明TSR可能对深埋储层的改善具有促进作用。这些认识有助于指导深层寒武系碳酸盐岩储层的进一步勘探。  相似文献   

17.
Petrographic examination of the dolomitized Main Limestone Series cropping out in the south, east and northeast corners of the South Wales Coalfield Basin shows evidence of the earlier presence of evaporite minerals. However, it is believed that lack of extensive evaporite deposits in these rocks may be due to the active diagenetic dissolution and oncoming humid coal conditions of post Main Limestone time.The evaporite minerals in the Main Limestone rocks seem to be overwhelmingly early diagenetic in origin in the light of the following observations: (1) calcite or dolomite pseudomorphs after gypsum crystals associated with a fine pelmicrite matrix; (2) association of such pseudomorphs with oolitic pelsparite; and (3) evaporite solution breccia texture.  相似文献   

18.
The question of a primary versus diagenetic origin for the limestone-shale rhythms of the Blue Lias has been addressed through a study of pyrite abundance and isotopic composition. Pyrite is relatively abundant and isotopically light in the central portions of the bioturbated limestones as compared to adjacent, less calcareous, sediment. The abundance of pyrite shows that the limestones were a focus for prolonged sulphate reduction and pyrite formation. The isotopic data indicate that bioturbation oxidized some pyrite to produce isotopically light sulphate, part of which was subsequently reduced back to pyrite before preservation by burial. Acidity generated by pyrite oxidation was buffered in the limestones by carbonate dissolution, hence supersaturation of sulphides could be maintained. By contrast, in adjacent less calcareous sediments, carbonate dissolution was unable to buffer acidity and bioturbational oxidation of pyrite formed iron-rich pore solutions. Continued sulphate reduction in the limestones acted as a sink for iron from the adjacent sediments and, with burial below the zone of bioturbation, the alkalinity so generated caused cementation of the limestones. Diagenetic cementation would be enhanced during an hiatus in sedimentation, an event which might be related to a Milankovitch forcing mechanism, but which would not be recorded in bioturbated, less calcareous sediment, thus leaving an imperfect record. Only cyclicity in pre-diagenetic sedimentation patterns may be safely related to a Milankovitch forcing mechanism as proposed by Weedon.  相似文献   

19.
Field, petrographic and stable isotopic evidence indicate the former presence of widespread evaporites in the Neoarchaean Campbellrand Subgroup of South Africa. Calcitization of the vanished but once laterally-extensive evaporites was apparently driven by bacterial sulphate reduction of solid sulphate in association with organic diagenesis and pyrite precipitation within platform-wide microbialites and sapropels. This counters current interpretations that much of the calcite was precipitated directly on the seafloor or in primary voids in open marine conditions controlled by regional seawater chemistry. Rather, large-scale microbial mediation of ambient waters across a shallow to emergent platform raised carbonate alkalinity and removed kinetic inhibitors to carbonate formation.The low preservation potential of Precambrian solid sulphate is related in part to bacterial sulphate reduction within the microbially-dominated ecosystems of which cyanobacteria were a major component. Evidence for the former presence of solid sulphate in shallow Neoarchaean seas includes pseudomorphs after selenite, also recorded from the contemporaneous Carawine Dolomite of Australia, together with rock fabrics and textures typical of evaporite dissolution. Importantly, sulphur isotopes of pyrite samples from the Cambellrand carbonates show a wide range of values indicating biogenic fractionation of sulphate, a signature also seen in the Neoarchaean Belingwe Greenstone Belt of Zimbabwe, and the Mt McRae and Jeerinah shales of Western Australia.Mass microbial colonization across extensive Neoarchaean epeiric seas witnessed the microbiogeochemical transformation of the Earth’s hydrosphere, atmosphere and biosphere. The consequences for a reducing ocean would be the progressive oxidation of the major dissolved species in surface seawater, most notably of reduced sulphur and iron. Cyanobacterial photosynthetic oxidation of surface seawater drove formation of aqueous sulphate and permitted the precipitation of extensive evaporites in restricted basins, perhaps beginning the process of ridding the oceans of reduced sulphur. The first dramatic explosion of carbonate precipitation can be related to intense bacterial sulphate reduction in association with anoxic organic diagenesis and pyrite formation within the decaying interiors of microbialites and in sapropels.  相似文献   

20.
利用岩芯和薄片资料,通过薄片孔隙描述、铸体薄片图像分析等方法,在对研究区马五41储层孔隙类型划分的基础上,详细划分了膏模孔充填类型,并对其充填过程进行了阐述。研究结果表明,研究区马五41储层主要发育溶蚀孔（膏模孔和其他溶孔）、晶间孔、晶间溶孔、微裂缝4种类型的孔隙,且以膏模孔为主。通过镜下薄片对膏模孔内不同充填物观察发现,充填物主要为白云石、方解石、硬石膏,其中半充填的膏模孔中主要充填物为白云岩粉砂、白云岩粉砂+石英、白云岩粉砂+铁白云石3种类型,而全充填的膏模孔中主要充填物为白云岩粉砂+方解石、白云岩粉砂+石英+方解石、白云岩粉砂+硬石膏3种类型。综合分析认为膏模孔是含膏云岩中石膏等易溶晶体溶蚀后,晶体轮廓保留而形成的,首先裸露风化壳期先充填白云岩粉砂和深灰色方解石,其次深埋藏期充填自生石英、白色亮晶方解石、铁白云石及硬石膏。  相似文献   

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