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1.
Detailed studies of a new, complete Marl Slate core in South Yorkshire have provided information on isotopic (δ13C, δ18O, δ34S) and geochemical variations (trace elements and C/S ratio) which enable the formulation of a model for carbonate and sulphide precipitation in the Late Permian Zechstein Sea. Calcite and dolomite are intimately associated; the fine lamination, organic character and absence of benthos in the sediments are indicative of anoxic conditions. Lithologically the core can be divided into a lower, predominantly sapropelic Marl Slate (2 m) and an upper Transition Zone (0·65 m) of alternating sapropel and calcite-rich and dolomite-rich carbonates. C/S ratios are 2·22 for the Marl Slate and 1·72 for the Transition Zone respectively, both characteristic of anoxic environments. δ18O in the carbonates shows a large and systematic variation closely mirrored by variations in calcite/dolomite ratio. The results suggest a fractionation factor equivalent to a depletion of 3·8% for 18O and 1·5% for 13C in calcite. The δ34S values of pyrite are isotopically light (mean value = - 32·7%) suggesting a fractionation factor for the Marl Slate of almost 44%, typical of anoxic basins. The results are related to stratification in the early Zechstein Sea. Calcite was precipitated in oxic upper layers above the halocline. Below the oxic/anoxic boundary framboidal pyrite was precipitated, resulting in lower sulphate concentration and elevated Mg/Ca ratio (due to calcite precipitation). As a result of this, dolomite formation occurred below the oxic/anoxic interface, within the anoxic water column and in bottom sediments. Variations in calcite/dolomite ratios, and isotopic variations, are thus explained by fluctuations in the relative level of the oxic/anoxic boundary in the Zechstein Sea.  相似文献   

2.
刘新宇  颜佳新 《沉积学报》2007,25(5):730-736
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。  相似文献   

3.
J. B. KEENE 《Sedimentology》1983,30(3):449-454
ABSTRACT Chalcedony is the most abundant form of quartz in silicified pelagic sediments from the North Pacific. Varieties of chalcedonic quartz present in chert of deep-sea origin include chalcedony (length-fast and zebraic), quartzine (length-slow), and lutecite.
These occurrences of quartzine in known pelagic sediments emphasize the dangers of using quartzine as an indicator of former evaporitic environments. Quartzine is a diagenetic mineral and does indicate pore fluids rich in sulphate and magnesium. In pelagic sediments, it is always associated with authigenic barite and in many cases with authigenic dolomite. Quartzine should not be used, by itself, as an indicator of any particular environment of deposition.  相似文献   

4.
Auriferous quartz pebble conglomerates (QPC) formed during Tertiary sedimentary recycling in the Waimumu district, Southland, New Zealand. These sediments contain fine-grained gold of detrital origin with abundant surface textures and gold-forms associated with authigenic gold remobilisation. Most authigenic gold contains no detectable silver and occurs as overgrowths on detrital Au–Ag and Au–Ag–Hg alloys that contain up to 13 wt.% Ag, and 9 wt.% Hg. Fine-grained Au–Ag and Au–Ag–Hg alloys are compositionally heterogeneous, exhibiting both well-defined silver-depleted and silver-enriched rims. Rare coarse Au–Ag alloy is intergrown with quartz and is homogenous. Discrete grains of authigenic, porous, sheet-like gold occur in carbonaceous mudstone within a QPC sequence. Some QPC contain abundant sulphide minerals. Some of these sulphides (pyrite and arsenopyrite) are of long-distance detrital origin, presumably from the Otago Schist, whereas the bulk of the sulphide suite is marcasite of variably transported diagenetic origin, derived from the erosion of QPC and underlying Tertiary sediments. There has also been authigenic deposition of sulphide minerals in the QPC themselves. These diagenetic sulphides include framboidal and anhedral marcasite, and framboidal and euhedral pyrite. Sulphur isotope data for the sulphide minerals range from − 45‰ to + 18‰ (relative to VCDT). Sulphur isotope data for euhedral detrital pyrite and arsenopyrite range from − 9‰ to − 1‰ and are most likely derived from the Otago Schist to the north. Both framboidal and anhedral marcasite have lower values (< − 20‰) reflecting microbial sulphate reduction as a source for the precursor hydrogen sulphide. Anhedral marcasite contains elevated concentrations of Ni, Co, As and Cr, commonly with compositional banding of these metals.Both the gold and diagenetic sulphides from the Belle-Brook QPC are compositionally similar to gold and sulphides from Archaean QPC. Porous, sheet-like authigenic gold is morphologically similar to gold associated with carbonaceous material in the Witwatersrand. In addition, Southland marcasite textures resemble the rounded and banded pyrite in Witwatersrand QPC placers. There is abundant evidence from these Tertiary QPC in southern New Zealand for sedimentary transport of sulphide minerals and post-depositional sulphide mineralisation in the surficial environment despite an oxygen-rich atmosphere. These young deposits thus provide an example of authigenic gold and sulphide textures formed during diagenesis in unmetamorphosed placers. Many of these textures are similar to those commonly ascribed to metamorphic processes in Archaean auriferous QPC.  相似文献   

5.
Tectonically isolated blocks of carbonate rocks present within the anhydritic Haselgebirge mélange of the Northern Calcareous Alps record a complex history of deformation and associated deep-burial diagenetic to very low-grade metamorphic reactions. Fluids were hot (up to ≈ 250 °C) and reducing brines charged with carbon dioxide. Individual carbonate outcrops within the mélange record different regimes of brine–rock reactions, ranging from pervasive dolomite recrystallization to dedolomitization. Early diagenetic features in these carbonates were almost entirely obliterated. Matrix dolomite alteration was related to thermochemical sulphate reduction (TSR) recognized by the replacement of anhydrite by calcite + pyrite ± native sulphur. Pyrite associated with TSR is coarsely crystalline and characterized by a small sulphur isotope fractionation relative to the precursor Permian anhydrite. Carbonates associated with TSR show low Fe/Mn ratios reflecting rapid reaction of ferrous iron during sulphide precipitation. As a result, TSR-related dolomite and calcite typically show bright Mn(II)-activated cathodoluminescence in contrast to the dull cathodoluminescence of many (ferroan) carbonate cements in other deep-burial settings. In addition to carbonates and sulphides, silicates formed closely related to TSR, including quartz, K-feldspar, albite and K-mica. 40Ar/39Ar analysis of authigenic K-feldspar yielded mostly disturbed step-heating spectra which suggest variable cooling through the argon retention interval for microcline during the Late Jurassic. This timing coincides with the recently recognized subduction and closure of the Meliata-Hallstatt ocean to the south of the Northern Calcareous Alps and strongly suggests that the observed deep-burial fluid–rock reactions were related to Jurassic deformation and mélange formation of these Permian evaporites.  相似文献   

6.
The stratiform Cu–Co ore mineralisation in the Katangan Copperbelt consists of dispersed sulphides and sulphides in nodules and lenses, which are often pseudomorphs after evaporites. Two types of pseudomorphs can be distinguished in the nodules and lenses. In type 1 examples, dolomite precipitated first and was subsequently replaced by Cu–Co sulphides and authigenic quartz, whereas in type 2 examples, authigenic quartz and Cu–Co sulphides precipitated prior to dolomite and are coarse-grained. The sulphur isotopic composition of the copper–cobalt sulphides in the type 1 pseudomorphs is between −10.3 and 3.1‰ relative to the Vienna Canyon Diablo Troilite, indicating that the sulphide component was derived from bacterial sulphate reduction (BSR). The generation of during this process caused the precipitation and replacement of anhydrite by dolomite. A second product of BSR is the generation of H2S, resulting in the precipitation of Cu–Co sulphides from the mineralising fluids. Initial sulphide precipitation occurred along the rim of the pseudomorphs and continued towards the core. Precipitation of authigenic quartz was most likely induced by a pH decrease during sulphide precipitation. Fluid inclusion data from quartz indicate the presence of a high-salinity (8–18 eq. wt.% NaCl) fluid, possibly derived from evaporated seawater which migrated through the deep subsurface. 87Sr/86Sr ratios of dolomite in type 1 nodules range between 0.71012 and 0.73576, significantly more radiogenic than the strontium isotopic composition of Neoproterozoic marine carbonates (87Sr/86Sr = 0.7056–0.7087). This suggests intense interaction with siliciclastic sedimentary rocks and/or the granitic basement. The low carbon isotopic composition of the dolomite in the pseudomorphs (−7.02 and −9.93‰ relative to the Vienna Pee Dee Belemnite, V-PDB) compared to the host rock dolomite (−4.90 and +1.31‰ V-PDB) resulted from the oxidation of organic matter during BSR.  相似文献   

7.
The Callovian-Oxfordian (COx) clayey unit is being studied in the Eastern part of the Paris Basin at depths between 400 and 500 m depth to assess of its suitability for nuclear waste disposal. The present study combines new mineralogical and isotopic data to describe the sedimentary history of the COx unit. Petrologic study provided evidence of the following diagenetic mineral sequence: (1) framboidal pyrite and micritic calcite, (2) iron-rich euhedral carbonates (ankerite, sideroplesite) and glauconite (3) limpid calcite and dolomite and celestite infilling residual porosity in bioclasts and cracks, (4) chalcedony, (5) quartz/calcite. Pyrite in bioturbations shows a wide range of δ34S (−38‰ to +34.5‰), providing evidence of bacterial sulphate reduction processes in changing sedimentation conditions. The most negative values (−38‰ to −22‰), measured in the lower part of the COx unit indicate precipitation of pyrite in a marine environment with a continuous sulphate supply. The most positive pyrite δ34S values (−14‰ up to +34.5‰) in the upper part of the COx unit indicate pyrite precipitation in a closed system. Celestite δ34S values reflect the last evolutionary stage of the system when bacterial activity ended; however its deposition cannot be possible without sulphate supply due to carbonate bioclast dissolution. The 87Sr/86Sr ratio of celestite (0.706872-0.707040) is consistent with deposition from Jurassic marine-derived waters. Carbon and oxygen isotopic compositions of bulk calcite and dolomite are consistent with marine carbonates. Siderite, only present in the maximum clay zone, has chemical composition and δ18O consistent with a marine environment. Its δ13C is however lower than those of marine carbonates, suggesting a contribution of 13C-depleted carbon from degradation of organic matter. δ18O values of diagenetic chalcedony range between +27‰ and +31‰, suggesting precipitation from marine-derived pore waters. Late calcite crosscutting a vein filled with chalcedony and celestite, and late euhedral quartz in a limestone from the top of the formation have lower δ18O values (∼+19‰), suggesting that they precipitated from meteoric fluids, isotopically close to present-day pore waters of the formation. Finally, the study illustrates the transition from very active, biotic diagenesis to abiotic diagenesis. This transition appears to be driven by compaction of the sediment, which inhibited movement of bacterial cells by reduction of porosity and pore sizes, rather than a lack of inorganic carbon or sulphates.  相似文献   

8.
Nodular silica concentrations reminiscent of evaporite bodies have been observed in the Late Precambrian (Riphean) Porsangerfjord Group in western Porsangerfjord, northern Norway. The nodules are individual or coalescent kidney-shaped bodies measuring a few centimetres across, and consist predominantly of megaquartz and of length-slow chalcedony. Length-fast chalcedony occurs only as a red layer present in some large nodules. Relics of a fibrous, felted or radiating texture are preserved in numerous crystals of megaquartz and quartzine.The quartz nodules are interpreted as silica-replaced, early diagenetic evaporite (anhydrite) bodies. The paleoclimatic importance of these Precambrian evaporites is briefly discussed and the significance of length-slow chalcedony as an indicator of evaporite environments is confirmed.  相似文献   

9.
Three major types of dolomite occur in the Trenton Formation (Mid-Ordovician) of the Michigan Basin. These are: (1) ‘regional dolomite’ which is confined to the extreme western edge of the basin; (2) ‘cap dolomite’ which occurs in the upper portion of the Trenton and is confined to the basin's southern margin; and (3) ‘fracture-related’ dolomite which occurs in association with both large- and small-scale faults and fractures. These three dolomite types can be distinguished from one another by their major element chemistry, oxygen isotope ratios and rock texture. The regional dolomite is fine-grained, has <0.34 mol% FeCO3, and mean δ18O of ?6·8‰OPBD. The cap dolomite is texturally similar to regional dolomite but contains 3–13·0 mol% FeCO3 and has a mean δ18O of ?7·7‰. Fracture-related dolomites are coarse-grained, low in iron, and have the most depleted δ18O ratios (x?=–9·0%PDB). Petrographic relationships imply that the regional dolomite, formed prior to the cap dolomite probably during early diagenesis. The cap dolomite formed at relatively shallow depths as a result of the interaction of the overlying Utica Shale and the Trenton Limestone. Fracture-related dolomites post-date the cap dolomite and formed during deeper burial. A temperature of precipitation of approximately 80°C was calculated for fracture-related dolomites using oxygen isotope data. The distribution of the cap dolomite was controlled by the availability of Fe2? which was in turn controlled by the availability of S2?. In the centre of the basin Trenton-Utica deposition was continuous. The upper Trenton contained relatively high concentrations of organic matter which was used by sulphate reducing bacteria to produce H2S from seawater sulphate. The precipitation of iron sulphides (pyrite + iron monosulphide) followed and used up most of the available Fe2?. As a result only small amounts of ferroan dolomite formed. On the periphery of the basin, subaerial exposure resulted in the oxidation of most of the available organic matter. Sulphate reducing bacteria were therefore limited and produced limited amounts of H2S. As a result only a minor amount of iron sulphide (iron monosulphide) formed. The remaining Fe2- was then available for the formation of the ferroan cap dolomite. This model is supported by the following: (1) In the southern margin of the basin, the contact between Trenton cap dolomite and the overlying Utica Shale is sharp and probably unconformable. In the centre of the basin the contact is gradational. (2) In the centre of the basin, the total organic carbon content in the upper Trenton is an order of magnitude higher than in the cap dolomite. (3) The whole-rock concentration of iron is high in both the cap dolomite and in slightly dolomitized equivalent beds in the basin centre. (4) Iron sulphides are abundant in the centre of the basin and mostly in the form of pyrite. In the cap dolomite, iron sulphide is minor and primarily in the form of iron monosulphide.  相似文献   

10.
Pyrite masses composed of compacted pyrite framboids in chalcedony in weathered andesites at Allandale, New South Wales, Australia, show evidence of colloidal origin and contemporaneous deposition of pyrite and silica. Free framboids and framboidal clusters in the chalcedony show indications of crystallization into pyrite polyhedra and pyrite octahedra.  相似文献   

11.
Despite recent advances, diagenetic processes in fine-grained sediments are still relatively poorly understood. Key questions still to be resolved include the types of diagenetic minerals present in mudstones and the extent of element mobility in these low permeability systems. This study utilizes data from the Haynesville-Bossier Shale, USA, to analyze lithologies, discriminate authigenic phases and identify mobile elements during diagenesis. It has implications for understanding how authigenic minerals develop and the sources of those authigenic minerals in fine-grained sediments. On the basis of grain-size and mineralogy five lithologies are designated: (i) silica-rich argillaceous mudstones; (ii) argillaceous siliceous mudstones; (iii) mixed siliceous mudstones; (iv) mixed mudstones; and (v) authigenically-dominated mudstones. The diagenetic development of the Haynesville-Bossier Shale can be divided into early and late diagenesis. Ferroan and non-ferroan dolomite, framboidal pyrite and bioclast pore-filling kaolinite and calcite grain replacements and cements all formed during early diagenesis. Late diagenetic mineral phases include illite formed by the illitization of smectite, replacive and displacive chlorite, calcite-replacive albite, quartz-replacive calcite and replacive and/or displacive quartz. The presence of extensive late diagenetic mineral precipitates indicates that there was a degree of element mobility on at least the local scale. Aluminium present in albite is most likely to have resulted from the illitization of smectite. Quartz overgrowths probably resulted from illitization and the pressure dissolution at quartz silt grain boundaries. Externally, hydrothermal fluids resulting from regional-scale igneous activity appear to have played a role in the formation of chlorite and possibly albite. The work indicates that extensive mineral development and element mobility occurred during late diagenesis.  相似文献   

12.
The Ediacara mineral field is situated 30 km W of Beltana on the western margins of the Flinders Ranges, South Australia, and consists of silver‐lead and copper deposits in lower Cambrian carbonate rocks that contain anomalous base‐metal contents throughout the Adelaide Geosyncline. The lower Cambrian rocks, which consist of the basal Parachilna Formation and overlying Ajax Limestone, rest disconformably on the Precambrian, and at Ediacara occupy a shallow N‐S elongate syncline near the hinge zone of the Adelaide Geosyncline. The main primary ore minerals of the silver‐lead mineralization are galena and pyrite, with very minor chalcopyrite and sphalerite, and rare tetrahedrite and pearceite. The gangue consists mainly of silica (both chalcedony and quartz), with minor dolomite and rare barite. The mineralization is stratabound and occurs in conformable zones, the lowest of which commences about 30–50 m above the base of the Cambrian sequence. The host to the silver‐lead mineralization, the Ajax Limestone, can be subdivided into three units which represent a set of lithologies, structures and organic traces indicative of a shallow near‐shore carbonate environment. The silver‐lead mineralization is mainly present in sandy and laminated dolomites which were deposited in an environment ranging from sub‐tidal to bar and channel and tidal flat, respectively. Four types of mineralization have been recognized; disseminated sulphides of syngenetic and/or diagenetic origin and epigenetic concentrations along stylolites, in veins and as breccia fillings. Post‐depositional solution activity has affected a large proportion of the carbonate sequence. The effects of this activity range from stylolites through stylobreccias to solution collapse breccias. The epigenetic concentrations of mineralizations have apparently been formed by the remobilization of the disseminated sulphides during solution activity. The ore and gangue minerals of the epigenetic mineralization display both euhedral forms and distinct colloform banding, and framboidal textures have also been observed in both pyrite and galena. There is evidence of repeated episodic precipitation and no simple paragenetic sequence can be recognized. Fluid inclusions in silica and dolomite associated with the epigenetic mineralization have homogenization temperatures of 159 to 199°C and freezing temperatures that indicate the fluids to be saline brines containing NaCl with CaCl2 and/or MgCl2. Sulphur isotope analyses show a range of 834S values from ‐12.5 to +8.6 per mil, with no evidence of significant differences between the four types of mineralization. The data suggest deposition of the disseminated sulphides as a result of biological reduction of seawater sulphate in a system partially open with respect to sulphate supply. Subsequent remobilization of sulphides apparently involved little or no sulphur isotope fractionation. The Ediacara silver‐lead deposits have many features in common with Mississippi Valley‐type lead‐zinc deposits and appear to have similarities in terms of genesis, in that the epigenetic mineralization has been formed as a result of post‐depositional solution activity during diagenesis in a sedimentary basin. The scale of transport of the metals deposited as the epigenetic mineralization at Ediacara appears, however, to have been very much less than that of the metals in other Mississippi Valley‐type deposits.  相似文献   

13.
Spheroidal dolomite crystals occur in the karstified top of a Dinantian dolomite sequence in eastern Belgium. The spheroidal dolomite crystals are best developed at the base of the karst system. The dolomite crystals are characterized by a spherulitic or dumb-bell inclusion pattern, and are overgrown by dolomite cements with a rhombohedral outline. They are considered to be bacterially related precipitates based on, (1) textural similarities with documented bacteriogenic precipitates, (2) the presence of ‘bacterial’microspheres and framboidal pyrite embedded within the dolomite, and (3) their general geological setting. The geochemical characteristics of the dolomites and associated minerals support a bacterial origin. The ubiquity of framboidal pyrite, depleted in 34S (δ34S=— 22.4 to — 25.5%oCDT), testifies to a period of bacterial sulphate reduction. The isotopic composition of the spheroidal dolomites (δ13C=— 2.4 to - 3.2%oPDB and δ18O=— 3.8 to - 3.4%oPDB) suggest a contribution from oxidized organic carbon produced during bacterial sulphate reduction. Sulphate reduction may also result in a concomitant 18O depletion if the system is nearly closed. It is however, evident from the sulphur isotopic composition of associated framboidal pyrite that the system was fairly open. The 18O depletion of the spheroidal dolomite crystals (δ18O=— 3.8 to — 3.4%oPDB) and their occurrence adjacent to, and within karst cavities suggests a mixing zone origin, with a significant proportion of freshwater in it. The rhombohedral cement-overgrowths have calculated δ18O values in the range of 0 to +5.3%oPDB, which reflect precipitation from normal to slightly evaporated contemporaneous seawater.  相似文献   

14.
Environments characterized by fluctuating hypersaline to fresh-water conditions are defined as “schizohaline” and examples are given of situations in which “schizohaline” environments can arise. Fabrics diagnostic for the occurrence of both hyper- and hyposalinity have been recorded in Late Paleozoic rocks from Bear Island (74°30′N, 19°E): evaporite nodules, length-slow chalcedony and very finely crystalline penecontemporaneous dolomite are considered as indicators of hypersaline conditions while euhedral limpid dolomite crystals, coarse poikilitic sparry calcite and microspar calcite are thought to have originated under the hyposaline regime. Zoned dolomite crystals and euhedral crystals of authigenic mega-quartz replacing sulphates have also been recorded in the same rocks; their diagnostic importance for the schizohaline environment is, however, uncertain.Internal structural pores of some crinoid and bryozoan skeletal grains of biosparites from Bear Island are either empty or infilled with very finely crystalline dolomite. Expulsion of Mg2+ ions from the magnesian-calcite skeletons and either: (1) “poisoning” of the micro-environment of the pores; or (2) formation of stagnant “micro-sabkha” conditions in the pores are proposed as an explanation for these phenomena.  相似文献   

15.
以层序地层研究为基础,根据铸体薄片、扫描电镜、镜质体反射率、X衍射及地球化学等分析,对东营凹陷沙河街组层序与成岩的关系进行了系统研究。研究结果表明:不同层序部位具有不同的成岩响应,低位体系域主要发育微晶方解石胶结、硬石膏胶结、黄铁矿胶结等,湖盆扩张体系域主要发育有铁碳酸盐胶结、粘土矿物胶结等;高位体系域主要发育有白云石胶结、铁白云石胶结、溶蚀作用、粘土矿物胶结等;层序界面附近主要发育溶蚀现象和铁碳酸盐岩胶结现象。层序发育过程中,原始水介质条件及元素富集规律是引起早期成岩响应的主要因素,并对早期的成岩物质组分造成强烈影响;讨论了层序对成岩演化的控制作用,主要体现在3个方面:a.层序发育控制了原始成岩组分,进而控制后期成岩改造;b.早期成岩作用对层序发育过程具有一定的响应关系,后期成岩改造掩盖了部分成岩响应;c.层序界面通过河流作用、沉积间断减缓压实作用、后期成岩流体的侵入作用对成岩演化造成影响。  相似文献   

16.
Development of a diagenetic anhydrite bed at the base of the Cretaceous Maha Sarakham Saline Formation (the `Basal Anhydrite' member) of the Khorat Plateau in north-eastern Thailand took place due to leaching and/or pressure dissolution of salt at the contact between an underlying active sandstone aquifer system and an overlying massive halite-dominated evaporite sequence. Basal evaporites composed of halite with intercalated anhydrite of the latter sequence are undergoing dissolution as a result of subsurface flushing, with anhydrite produced as the insoluble residue. The result is a 1·1 m thick interval of nodular anhydrite displaying unique, basin-wide continuity. Observed textures, petrographic features and chemical data from the anhydrite and associated authigenic minerals support the origin of the Basal Anhydrite Member as an accumulation residue from the dissolution of the Maha Sarakham salts. Petrographically, the anhydrite in this unit is made up of crystals that are blocky and recrystallized, sheared, generally elongated and broken, and is bounded at the bottom by organic-rich stylolite surfaces. Authigenic and euhedral dolomite and calcite crystals are associated with the anhydrite. Traces of pyrite, galena and chalcopyrite are present along the stylolite surfaces suggesting supply of fresh water from the underlying sandstone at highly reducing conditions of burial. The δ34S of sulphate in the Basal Anhydrite averages 15 ‰ (CDT) and falls within the isotopic composition of the anhydrite in the Cretaceous Maha Sarakham Formation proper and the Cretaceous values of marine evaporites. Measured δ18O in dolomite range from ?4·37 to ?14·26‰ (PDB) suggesting a re-equilibration of dolomite with basinal water depleted in 18O and possible recrystallization of dolomite under relatively elevated temperatures. The δ13C, however, varies from +1·57 to ?2·53‰ (PDB) suggesting a contribution of carbon from oxidation of organic matter. This basal anhydrite bed, similar to basinwide beds found at the bottom of many giant evaporite sequences, has always been considered to be depositional. Here, at the base of the Maha Sarakham Formation, we demonstrate that the anhydrite is diagenetic in origin and was formed by accumulation of original anhydrite by dissolution of interbedded halite from waters circulating though the underlying aquifer: it represents an `upside-down' caprock.  相似文献   

17.
Alpha Mound and Beta Mound are two cold‐water coral mounds, located on the Pen Duick Escarpment in the Gulf of Cadiz amidst the El Arraiche mud volcano field where focused fluid seepage occurs. Despite the proximity of Alpha Mound and Beta Mound, both mounds differ in their assemblage of authigenic minerals. Alpha Mound features dolomite, framboidal pyrite and gypsum, whereas Beta Mound contains a barite layer and predominantly euhedral pyrite. The diagenetic alteration of the sedimentary record of both mounds is strongly influenced by biogeochemical processes occurring at shallow sulphate methane transition zones. The combined sedimentological, petrographic and isotopic analyses of early diagenetic features in gravity cores from Alpha Mound and Beta Mound indicate that the contrast in mineral assemblages between these mounds is caused by differences in fluid and methane fluxes. Alpha Mound appears to be affected by strong fluctuations in the fluid flow, causing shifts in redox boundaries, whereas Beta Mound seems to be a less dynamic system. To a large extent, the diagenetic regimes within cold‐water coral mounds on the Pen Duick Escarpment appear to be controlled by fluid and methane fluxes deriving from layers underlying the mounds and forcings like pressure gradients caused by bottom current. However, it also becomes evident that authigenic mineral assemblages are not only very sensitive recorders of the diagenetic history of specific cold‐water coral mounds, but also affect diagenetic processes in turn. Dissolution of aragonite, lithification by precipitation of authigenic minerals and subsequent brecciation of these lithified layers may also exert a control on the advective and diffusive fluid flow within these mounds, providing a feedback mechanism on subsequent diagenetic processes.  相似文献   

18.
川东北地区石炭系成岩作用及储集性   总被引：1，自引：0，他引：1  
川东北石炭系为一套蒸发性局限海潮坪沉积 ,仅残存中石炭统黄龙组。残厚在通江—南江—巴中地区为2 0 -m左右 ,且分布零星 ;开县—大竹—垫江一带为主要分布区 ,达县地区最厚 ,局部可达 70 -m。岩性主要为含粒屑微—粉晶白云岩、角砾状白云岩、膏岩及泥晶灰岩等。经历了白云石化、重结晶、溶蚀等成岩作用和构造作用 ,地层的溶蚀孔、晶间孔和裂缝发育 ,其储集性能得到了较大改善 ,成为川东北乃至川东地区碳酸盐岩地层中最重要的一套储集层。孔隙度大于 3%的储层分布范围也在开县—大竹—垫江构造上 ,呈北东向展布。宣汉以北 ,主要是由于双石庙、通江—南江—巴中地区石炭系地层变薄 ,因而储集性能较差。高产的沙罐坪气藏预示本区石炭系具良好的油气远景。  相似文献   

19.
石膏对白云岩溶解影响的实验模拟研究   总被引：25，自引：2，他引：25  
黄思静  杨俊杰 《沉积学报》1996,14(1):103-109
表生到埋藏成岩作用的温度与压力（４０-１３０℃、常压－３０ＭＰａ）条件下，含膏与不含膏白云岩的溶解实验证明:在表生与相对浅埋藏的温压条件（低于７５℃，２０ＭＰａ）下，石膏（或硬石膏）的存在可不同程度地加速白云岩的溶解，随着实验温度和压力的升高，石膏（或硬石膏）对白云岩溶解的这种积极作用逐渐降低。在相对深埋藏的温压条件（高于７５℃、２０ＭＰａ）下，石膏（或硬石膏）的存在显著阻止白云岩的溶解，随着实验温度和压力的继续升高，石膏（或硬石膏）对白云岩溶解的这种消极作用也逐渐增加。从实验的这种结果可以预测，在近地表条件下和埋藏成岩作用的早期阶段，由溶解作用造成的含膏白云岩地层的次生孔隙将比不含膏的白云岩地层更为发育，因而在经历了古风化作用的地层中，含膏白云岩层更易形成良好的储层；与之相反，在相对高温高压的深埋藏成岩阶段，不含膏的白云岩地层中将更容易因酸性水的溶解作用而形成次生孔隙。因而在非蒸发沉积环境中形成的白云岩体（如正常海沉积环境的灰岩中的白云岩透镜体）更易因深埋藏溶蚀作用而形成良好的储层。  相似文献   

20.
Diagenesis in shallow cores from the Lower Cretaceous Edwards Limestone was investigated in thin sections and with the scanning electron microscope (SEM). The SEM is a particularly useful tool in the study of diagenesis in porous fine-grained carbonate rocks because of its good resolution and depth of field.The Edwards Group was deposited in shallow-marine environments and underwent normal early diagenesis. Dolomite and evaporite minerals such as gypsum formed penecontemporaneously in some tidal-flat sediments. Slightly later, when the carbonate sediments were flushed by fresh water, carbonate mud recrystallized to micrite and aragonite allochems altered to calcite or were leached. Some cementation by calcite occurred in a fresh-water phreatic environment.The Edwards Limestone was divided into two zones by Miocene faulting along the Balcones Fault Zone. On the upthrown side of the fault a circulating fresh-water aquifer developed, whereas relatively stagnant brackish water remained present on the down-thrown side. Differences in the chemistry of the interstitial fluids in these zones resulted in different types of diagenesis. The presence of fresh water caused extensive oxidation, solution along fractures, recrystallization of micrite to coarse microspar and pseudospar, precipitation of equant sparry-calcite crystals in a variety of shapes and sizes, and extensive dedolomitization. The dedolomitization is thought to have been caused by the high Ca/Mg ratio of the circulating fresh water in a shallow subsurface environment.In the brackish-water zone, textures and fabrics related to deposition or early diagenesis, such as primary porosity, unoxidized organic material, framboidal pyrite, and evaporite minerals have been preserved. Some precipitation of authigenic dolomite, celestite, and kaolinite occurred in the brackish-water zone. In contrast to the fresh-water zone, precipitation of coarse calcite spar, dedolomitization, and recrystallization of micrite to microspar occurred only rarely in the brackish-water zone.  相似文献   

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