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1.
The Darlington (Sakmarian) and Berriedale (Artinskian) Limestones are neritic deposits that accumulated in high‐latitude environments along the south‐eastern margin of Pangea in what is now Tasmania. These rocks underwent a series of diagenetic processes that began in the marine palaeoenvironment, continued during rapid burial and were profoundly modified by alteration associated with the intrusion of Mesozoic igneous rocks. Marine diagenesis was important but contradictory; although dissolution took place, there was also coeval precipitation of fibrous calcite cement, phosphate and glauconite, as well as calcitization of aragonite shells. These processes are interpreted as having been promoted by mixing of shelf and upwelling deep ocean waters and enabled by microbial degradation of organic matter. In contrast to warm‐water carbonates where meteoric diagenesis is important, the Darlington and Berriedale Limestones were largely unaffected by meteoric diagenesis. Only minor dissolution and local cementation took place in this diagenetic environment, although mechanical compaction was ubiquitous. Correlation with burial history curves indicates that chemical compaction became important as burial depths exceeded 150 m, promoting precipitation of extensive ferroan calcite. This effect resulted from burial by rapidly deposited, overlying, thick, late Permian and Triassic terrestrial sediments. This diagenetic pathway was, however, complicated by the subsequent intrusion of massive Mesozoic diabases and associated silicifying diagenetic fluids. Finally, fractures most probably connected with Cretaceous uplift were filled with late‐stage non‐ferroan calcite cement. This study suggests that both carbonate dissolution and precipitation occur in high‐latitude marine palaeoenvironments and, therefore, the cold‐water diagenetic realm is not always destructive in terms of diagenesis. Furthermore, it appears that for the early Permian of southern Pangea at least, there was no real difference in the diagenetic pathways taken by cool‐water and cold‐water carbonates. 相似文献
2.
New interpretations of Great Salt Lake ooids and of ancient non-skeletal carbonate mineralogy 总被引：2，自引：0，他引：2
PHILIP A. SANDBERG 《Sedimentology》1975,22(4):497-537
Earlier interpretations of textural alteration affecting Great Salt Lake ooids have greatly influenced concepts of ooid diagenesis. Scanning electron microscope study shows, however, that the coarse radial aragonite rays are depositional, that no recrystallization of pellet cores has occurred, and that Great Salt Lake ooids have not suffered noticeable diagenesis. As suggested by Kahle (1974), radial texture in ancient calcitic ooids is probably mainly original, not diagenetic. Retention of such fine textures has been attributed to organic matter (since found to be equivalent in modern skeletal and non-skeletal grains) or to paramorphic replacement (proposed for non-skeletal grains whose original aragonite mineralogy was only inferred from modern analogs). Pleistocene ooids known to have been aragonite alter like aragonite shells to coarse neomorphic calcite, often with aragonite relics. The striking uniformity of that coarse texture in neomorphic calcite replacing known skeletal aragonites throughout the geologic record has been noted for over 100 years. In contrast, Mississippian ooids retain fine texture as do calcite layers of coexisting gastropods, but unlike the strongly altered aragonite layers of these same gastropods. Therefore, inferences of original aragonitic mineralogy of ancient non-skeletal carbonate grains (including muds) which are now calcite but retain fine texture appear unwarranted, as do assumptions of differential diagenetic behaviour of ancient aragonitic skeletal and non-skeletal grains. Accordingly, modern depositional environments of marine ooids and carbonate muds must be rejected as chemically unrepresentative of comparable ancient environments. It is inferred that ancient non-skeletal carbonates were originally predominantly or exclusively calcite because of an earlier lower oceanic Mg/Ca ratio (<2/1) which altered progressively to values favouring aragonite (modern Mg/Ca value = 5/1). Major influencing factors are: selective removal of calcium by planktonic foraminifers and coccolithophorids since Jurassic-Cretaceous time and by abundant younger, Mg-poor aragonite skeletons and an erratic trend toward decreasing dolomite formation (decreasing removal of oceanic Mg). The change to aragonite dominance over calcite for non-skeletal carbonates was probably during early to middle Cenozoic time. 相似文献
3.
基于西沙永兴岛上最新钻孔（SSZK1）取得的55.92 m岩芯的 U?Th定年、矿物、薄片、主微量元素及碳氧稳定同位素等资料,开展了西沙群岛晚第四纪碳酸盐岩沉积相和淡水成岩作用的研究。根据不同的矿物组成特征,可将SSZK1钻孔岩芯分为上、中、下三段: 下 段（33.89~55.92 m,主要为低镁方解石）、中 段（18.39~33.89 m,主要为文石和低镁方解石）、上段（0~18.39 m,主要为文石、高镁方解石和低镁方解石）。由于下段碳酸盐岩几乎全为稳定的低镁方解石组成,碳氧同位素值的严重负偏和小幅度变化,可推断其经历了程度较大的淡水成岩作用。中段和上段还存在不稳定的文石和高镁方解石,碳氧同位素值相对下段正偏和高幅高频变化,推测其淡水成岩作用的程度比下段要小。中段碳氧同位素值高幅高频变化同时也说明该段的矿物纵向变化较复杂。这种矿物组成的复杂变化可能是由于晚第四纪海平面频繁变化,该段被大气水渗流带和潜流带交替占据引起的。主微量元素的变化同时受到淡水成岩作用和沉积环境的影响。在中段、下段中可识别出sq1、sq2、sq3、sq4四个完整的相旋回。Na2O,S,Sr 和碳氧同位素受到的淡水成岩作用而被消耗和负偏,且由于老一期的旋回经历了更长时间的淡水成岩作用,新、老旋回间的 Na2O,S,Sr含量值和碳氧同位素值有明显差异。利用新、老时期形成的旋回间淡水成岩作用剩余Na2O,S,Sr含量和碳氧同位素值的差别可以将新、老两个旋回区分开来。 相似文献
4.
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. 相似文献
5.
Cathodoluminescent bimineralic ooids from the Pleistocene of the Florida continental shelf 总被引：1，自引：0，他引：1
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. 相似文献
6.
A strong correlation in the geometry and mineralogy of two cement generations of a Quaternary with a Precambrian calcarenite enables us to reconstruct the diagenetic history of the Precambrian limestone. Both calcarenites contain two cement generations (A and B) of which A consists of dolomite, B of calcite. The following diagenetic stages can be recognized: after deposition of the allochems in a shallow marine environment, cementation in the intertidal zone with magnesian calcite (cement A) led to the formation of beachrock (Stage 1). By lowering of the sea level, the beach rock was shifted into the supratidal zone, but still remained under the predominant influence of the sea water (breakers, spray). During longer periods of aridity, the magnesian calcite of cement A and of the allochems was transformed into dolomite by brines derived from sea water with very high Mg/Ca ratio (> 15), whereas aragonite and calcite remained unaffected. After further lowering of the sea, an increasing influence of meteoric water caused the wet transformation of aragonitic allochems to sparry calcite and to the precipitation of sparry calcitic cement B. 相似文献
7.
The Permian Park City Formation consists of cyclically bedded subtidal to supratidal carbonates, cherts and siltstones. Early diagenesis of Park City Formation carbonates occurred under the influence of waters ranging from evaporative brines to dilute meteoric solutions and resulted in evaporite emplacement (syndepositional nodules and cements), as well as dolomitization, silicification and leaching of carbonate grains. Major differences are seen, however, in the diagenetic patterns of subsurface and surface sections of Park City Formation rocks. Subsurface samples are characterized by extensively preserved evaporite crystals and nodules, and preserve evidence of significant silicification (chert, chalcedony and megaquartz) and minor calcitization of evaporites. In outcrop sections, the evaporites are more poorly preserved, and have been replaced by silica and calcite and also leached. The resultant mouldic porosity is filled with widespread, very coarse, blocky calcite spar. These replacements appear to be multistage phenomena. Field and petrographic evidence indicates that silicification involved direct replacement of evaporites and occurred during the early stages of burial prior to hydrocarbon migration. Siliceous sponge spicules provided a major source of silica, and the fluids involved in replacement were probably a mixture of marine and meteoric waters. A second period of replacement and minor calcitization is inferred to have occurred during deep burial (under the influence of thermochemical sulphate reduction), although the presence of hydrocarbons probably retarded most other diagenetic reactions during this time interval. The major period of evaporite diagenesis, however, occurred during late stage uplift. The late stage replacement and pore-filling calcites have δ13C values ranging from 0·5 to -25·3%, and δ18O values of -16·1 to -24·30 (PDB), reflecting extensive modification by meteoric water. Vigorous groundwater flow, associated with mid-Tertiary block faulting, led to migration of meteoric fluids through the porous carbonates to depths of several kilometres. These waters reacted with the in situ hydrocarbon-rich pore fluids and evaporite minerals, and precipitated calcite cements. The Tosi Chert appears to have been an even more open system to fluid migration during its burial and has undergone a much more complex diagenetic history, as evidenced by multiple episodes of silicification, calcitization (ferroan and non-ferroan), and hydrocarbon emplacement. The multistage replacement processes described here do not appear to be restricted to the Permian of Wyoming. Similarly complex patterns of alteration have been noted in the Permian of west Texas, New Mexico, Greenland and other areas, as well as in strata of other ages. Thus, multistage evaporite dissolution and replacement may well be the norm rather than the exception in the geological record. 相似文献
8.
AXEL MUNNECKE HILDEGARD WESTPHAL† JOHN J. G. REIJMER† CHRISTIAN SAMTLEBEN 《Sedimentology》1997,44(6):977-990
Comparison of ultrastructures in Pliocene periplatform carbonates from the Bahamas with Silurian limestones from Gotland (Sweden) reveals that despite the differences in primary sediment composition and age, they reflect a similar mechanism of lithification. In both sequences calcite microspar was formed as a primary cement at an early stage of marine burial diagenesis. Neither significant compression nor meteoric influence are necessary for the formation of calcite microspar. A model is proposed for the process of microsparitic cementation of fine-grained aragonite needle muds comprising four stages: (1) unconsolidated, aragonite-dominated carbonate mud; (2) precipitation of microspar that engulfs aragonite needles; (3) dissolution of aragonite, resulting in pitted surfaces of the microspar crystals; and (4) slight recrystallization. Our results contradict the widespread opinion that microspar necessarily is a product of secondary recrystallization of a previously lithified micrite. 相似文献
9.
更新世以来,剧烈的构造运动已将巴布亚新几内亚合恩半岛东北海岸的晚第四纪珊瑚礁阶地抬升上千米.阶地中造礁珊瑚的成岩变化和成岩产物的组构特征反映了该礁的成岩历史,充分体现该区快速构造上升的影响.海水潜流带和淡水渗流带为上升礁的主要成岩环境.生物钻孔、生物碎屑填隙、珊瑚文石针粗化、珊瑚骨骼的溶解和新生变形转化,以及其不同矿物成分和组构的种种胶结物的胶结作用是造礁珊瑚经历的主要成岩作用.地球化学资料表明其成岩变化发生于开放的化学体系之中. 相似文献
10.
Calcite cementation during bacterial manganese, iron and sulphate reduction in Jurassic shallow marine carbonates 总被引：4，自引：0，他引：4
JAMES P. HENDRY 《Sedimentology》1993,40(1):87-106
Faunally restricted argillaceous wackestones from the Middle Jurassic of eastern England contain evidence of early diagenetic skeletal aragonite dissolution and stabilization of the carbonate matrix, closely followed by precipitation of zoned calcite cements, and precipitation of pyrite. Distinctive cathodoluminescence and trace element trends through the authigenic calcites, their negative δ13C compositions and the location of pyrite in the paragenetic sequence indicate that calcite precipitation took place during sequential bacterial Mn, Fe and sulphate reduction. Calcite δ18O values are compatible with cementation from essentially marine pore fluids, although compositions vary owing to minor contamination with 18O-depleted ‘late’cements. Mg and Sr concentrations in the calcites are lower than those in recent marine calcite cements. This may be a result of kinetic factors associated with the shallow burial cementation microenvironments. Bicarbonate for sustained precipitation of the authigenic calcites was derived largely from aragonite remobilization, augmented by that produced through anaerobic organic matter oxidation in the metal and sulphate reduction environments. Aragonite dissolution is thought to have been induced by acidity generated during aerobic bacterial oxidation of organic matter. Distinction of post-oxic metal reduction and anoxic sulphate reduction diagenetic environments in modern carbonate sediments is uncommon outside pelagic settings, and early bacterially mediated diagenesis in modern platform carbonates is associated with extensive carbonate dissolution. High detrital Fe contents of the Jurassic sediments, and their restricted depositional environment, were probably the critical factors promoting early cementation. These precipitates constitute a unique example of calcite authigenesis in shallow water limestones during bacterial Mn and Fe reduction. 相似文献
11.
Paleoclimate of some Permo-Triassic carbonates of Malaysia 总被引：1，自引：0，他引：1
C. Prasada Rao 《Sedimentary Geology》1988,60(1-4):163-171
Four hundred thin-sections of Permian (Chuping and Summalayang Limestones) and Triassic (Kodiang Limestone) carbonates of Malaysia were studied, mainly to interpret probable climatic zones during their formation.
Chuping Limestone is rich in skeletal grains and intraclasts formed in shallow, high-energy environments. Original mineralogy of skeletal grains and early diagenetic cements were chiefly calcites with some aragonite. The faunal assemblage is similar to that of subpolar carbonates. The brachiopods are characterized by heavy δ13C and light δ18O and these values lie in the same field as an Early Permian fauna from eastern Australia. The δ18O values of fauna show unrealistic temperatures because the fauna has equilibrated with melt waters. However, calculated original δ18O values of the fauna from δ13C indicate temperatures ranging from 2 to 13°C with δw of +1.2. These features reflect cool-temperate (to ?subpolar) conditions.
Summalayang Limestone is rich in fusulinids and was deposited in bar to shelf environments. Fusulinids are often filled with fine, equigranular sparry calcite. Early diagenetic origin of these cements is indicated by erosion of cements during transportation and also by the cross-cutting relationship of veins with cements. These cements were originally Mg calcites. The foramol faunal assemblage, and predominantly Mg calcite mineralogy of both fauna and cements, reflect temperate climate.
Kodiang Limestone was deposited in peritidal environments. This limestone formation has all the characteristic features of modern, warm, tropical carbonates such as chlorozoan assemblage, diverse non-skeletal grains, abundant early diagenetic dolomites and predominance of aragonitic fauna, non-skeletal grains and cements.
The formation of temperate carbonates during the Permian suggests that Malaysia was probably part of Gondwanaland. 相似文献
12.
GREGORY E. WEBB LUKE D. NOTHDURFT BALZ S. KAMBER† J. T. KLOPROGGE‡ JIAN-XIN ZHAO§ 《Sedimentology》2009,56(5):1433-1463
Rare earth element geochemistry in carbonate rocks is utilized increasingly for studying both modern oceans and palaeoceanography, with additional applications for investigating water–rock interactions in groundwater and carbonate diagenesis. However, the study of rare earth element geochemistry in ancient rocks requires the preservation of their distribution patterns through subsequent diagenesis. The subjects of this study, Pleistocene scleractinian coral skeletons from Windley Key, Florida, have undergone partial to complete neomorphism from aragonite to calcite in a meteoric setting; they allow direct comparison of rare earth element distributions in original coral skeleton and in neomorphic calcite. Neomorphism occurred in a vadose setting along a thin film, with degradation of organic matter playing an initial role in controlling the morphology of the diagenetic front. As expected, minor element concentrations vary significantly between skeletal aragonite and neomorphic calcite, with Sr, Ba and U decreasing in concentration and Mn increasing in concentration in the calcite, suggesting that neomorphism took place in an open system. However, rare earth elements were largely retained during neomorphism, with precipitating cements taking up excess rare earth elements released from dissolved carbonates from higher in the karst system. Preserved rare earth element patterns in the stabilized calcite closely reflect the original rare earth element patterns of the corals and associated reef carbonates. However, minor increases in light rare earth element depletion and negative Ce anomalies may reflect shallow oxidized groundwater processes, whereas decreasing light rare earth element depletion may reflect mixing of rare earth elements from associated microbialites or contamination from insoluble residues. Regardless of these minor disturbances, the results indicate that rare earth elements, unlike many minor elements, behave very conservatively during meteoric diagenesis. As the meteoric transformation of aragonite to calcite is a near worst case scenario for survival of original marine trace element distributions, this study suggests that original rare earth element patterns may commonly be preserved in ancient limestones, thus providing support for the use of ancient marine limestones as proxies for marine rare earth element geochemistry. 相似文献
13.
Shells of the aragonite bivalve Neomiodon (Great Estuarine Group, Jurassic, Scotland) replaced by coarse neomorphic calcite contain oriented relics of the original aragonite ultrastructure. The presence of these relics in such old altered shells, as well as the high Sr content of the replacement calcite, indicate that the process of calcite replacement of aragonite is not a cumulative slow process involving repeated alteration events, but rather a rapid, one-step process. Aragonite relics, once encased in neomorphic spar, will survive as unequivocal evidence of original aragonite mineralogy, barring total remobilization of the enclosing stable calcite, a generally unlikely event. The retention of this residual aragonite and high-Sr calcite supports recent isotopic studies which suggest that the multiple phases of alteration (‘recrystallization’) invoked in earlier literature are unlikely events in the diagenesis of most undolomitized limestones. Retention of aragonite relics appears to be independent of whether alteration occurs in shallow meteoric or, as in the case of our Neomiodon material, deeper burial environments. Pseudopleochroism of the replaced Neomiodon shells appears to be due to organic, largely graphitic, relics, not to the aragonite relics. 相似文献
14.
Thomas Mann Andr Wizemann Marleen Stuhr Yannis Kappelmann Alexander Janßen Jamaluddin Jompa Hildegard Westphal 《Sedimentology》2022,69(1):282-300
Early-diagenetic cementation of tropical carbonates results from the combination of numerous physico-chemical and biological processes. In the marine phreatic environment it represents an essential mechanism for the development and stabilization of carbonate platforms. However, diagenetic cements that developed early in the marine phreatic environment are likely to become obliterated during later stages of meteoric or burial diagenesis. When lithified sediment samples are studied, this complicates the recognition of processes involved in early cementation, and their geological implications. In this contribution, a petrographic microfacies analysis of Holocene Halimeda segments collected on a coral island in the Spermonde Archipelago, Indonesia, is presented. Through electron microscopical analyses of polished samples, this study shows that segments are characterized by intragranular cementation of fibrous aragonite, equant High-Mg calcite (3.9 to 7.2 Mol% Mg), bladed Low-Mg calcite (0.4 to 1.0 Mol% Mg) and mini-micritic Low-Mg calcite (3.2 to 3.3 Mol% Mg). The co-existence and consecutive development of fibrous aragonite and equant High-Mg calcite results initially from the flow of oversaturated seawater along the aragonite template of the Halimeda skeleton, followed by an adjustment of cement mineralogy towards High-Mg calcite as a result of reduced permeability and fluid flow rates in the pores. Growth of bladed Low-Mg calcite cements on top of etched substrates of equant High-Mg calcite is explained by shifts in pore water pH and alkalinity through microbial sulphate reduction. Microbial activity appears to be the main trigger for the precipitation of mini-micritic Low-Mg calcite as well, based on the presumable detection of an extracellular polymeric matrix during an early stage of mini-micrite Low-Mg calcite cement precipitation. Radiocarbon analyses of five Halimeda segments furthermore indicate that virtually complete intragranular cementation in the marine phreatic environment with thermodynamically/kinetically controlled aragonite and High-Mg calcite takes place in about 100 years. Collectively, this study shows that early-diagenetic cements are highly diverse and provides new quantitative constraints on the rate of diagenetic cementation in tropical carbonate factories. 相似文献
15.
Middle Pleistocene to Holocene sediment variations observed in a 26 metre long core taken during a cruise of the RV Marion Dufresne are presented. Core MD992202 was retrieved from the northern slope of Little Bahama Bank and provides an excellent example for sedimentation processes in a mid‐slope depositional environment. The sediment composition indicates sea‐level related deposition processes for the past 375 000 years (marine isotope stages 1 to 11). The sediments consist of: (i) periplatform ooze (fine‐grained particles of shallow‐water and pelagic origin) with moderate variations in carbonate content, carbonate mineralogy and grain‐size; and (ii) coarser intervals with cemented debris consisting of massive, poorly sorted, mud‐supported or clast‐supported deposits with an increased high‐magnesium calcite content. During interglacial stages (marine isotope stages 1, 5, 7, 9 and 11) periplatform oozes (i) are characterized by higher aragonite contents, finer grain‐size and higher organic contents, whereas during glacial stages (marine isotope stages 2 to 4, 6, 8 and 10), increased low‐magnesium and high‐magnesium calcite values, coarser grain‐size and lower organic contents are recorded. These glacial to interglacial differences in mineralogy, grain‐size distribution and organic content clearly show the impact of climatically controlled sea‐level fluctuations on the sedimentation patterns of the northern slope of Little Bahama Bank. The coarser deposits (ii) occur mainly at the transitions from glacial to interglacial and interglacial to glacial stages, and are interpreted as redeposition events, indicating a direct link between sediment properties (changes in mineralogy, grain‐size distribution, variations in organic contents) and sea‐level fluctuations. Changes in hydrostatic pressure and the wave base position during sea‐level changes are proposed to have triggered these large‐scale sediment redepositions. 相似文献
16.
A marked increase in manganese content from shallow to deep marine lithofacies can be observed within the carbonate fraction of the Middle Ordovician sequence in eastern Tennessee. The distribution of manganese is controlled by: (1) the original aragonite and calcite mineralogy of shallow and deep marine environments, respectively; (2) preferential substitution of manganese for calcium in the rhombohedral structure of calcite; (3) anoxic depositional and diagenetic environments; and (4) possibly, volcanism. 相似文献
17.
Even with careful petrographic and mineralogic characterization of marine limestones, intertidally and subtidally lithified rocks are often difficult to differentiate, thus hindering an accurate delineation of the diagenetic environment. Limestones from water depths of 6 to 8 m off Kuwait vary in petrographic character from oosparite and biosparite (in which the cement is entirely aragonite) to oomicrite and biomicrite (in which at least some of the cement is microcrystalline magnesian calcite). Carbon-14 dates suggest that the oosparite may have lithified at depths shallower than at present (possibly intertidally) during a lower stand of sea-level. In contrast the biosparite, oomicrite and biomicrite appear to be contemporaneous and to have lithified subtidally. 相似文献
18.
The diagenesis of carbonate platform sediments is controlled by the original facies and mineralogy, climate, sea-level changes and burial history; these controls are clearly seen in the diagenesis of the Urgonian platform carbonates of SE France. Early diagenesis in the Urgonian platform included the precipitation of marine cements, dissolution of rudist shells and minor karstification. Diagenetic features produced during this phase were controlled by several falls in relative sea-level during the Barremian to mid-Aptian punctuating platform sedimentation, the original mineralogy of the sediment and the prevailing semi-arid/arid climate in the region at this time. Following a relative sea-level rise and further sedimentation, progressive burial of the platform led to minor compaction, followed by precipitation of coarse, equant, zoned to non-luminescent, calcite cement. This cement was cut by later stylolites, suggesting a relatively shallow-burial origin. Stable isotope (mean values - 7.94%δ18O and 0.36%δ13C) and trace element (mean values of Fe 334 ppm, Mn 92 ppm and Sr 213 ppm) data suggest that these cements precipitated from meteoric fluids at temperatures slightly elevated relative to depositional temperatures. A variable thickness of replacive dolomite which occurs preferentially within the shelf-margin facies of the lower part of the Urgonian post-dates mechanical fracturing and chemical compaction, but pre-dates the main phase of stylolitization. It is probable that the dolomitizing fluid was sourced by the early compaction-driven release of connate fluids held within the underlying muddy units. The burial history of these rocks suggests that calcite cementation and dolomitization took place at relatively shallow burial depths (1–1.5 km). The overall diagenetic history of the Urgonian Limestone Formation is a reflection of the pre-conditioning of the platform limestones by climate, sea level, tectonics and the shallow burial depths experienced by the platform during the later Mesozoic. 相似文献
19.
Relatively few studies have so far addressed diagenetic processes in Heterozoan carbonates and the role that sediment composition and depositional facies exert over diagenetic pathways. This paper presents a study of Oligocene shallow-water, Heterozoan carbonates from the Maltese Islands. We investigate stratigraphic distribution, abundance and timing of diagenetic features and their relationship to sediment composition and depositional facies. The studied carbonate rocks comprise rud- to packstones of the Heterozoan association predominantly containing coralline red algae, bryozoans, echinoids and benthic foraminifers. XRD analyses show that all high-Mg calcite has been transformed to low-Mg calcite and that no aragonite is preserved. Diagenetic processes include dissolution of aragonitic biota, neomorphism of high-Mg calcitic biota to low-Mg calcite and cementation by fibrous, bladed, epitaxial and blocky cements. Stable isotopes on bulk rock integrated with petrographic data suggest that the study interval was not exposed to significant meteoric diagenesis. We interpret early cementation to have taken place in the marine and marine burial environment. The distribution and abundance of early diagenetic features, determining the diagenetic pathway, can be related to the primary sediment composition and depositional texture. Sorting and micrite content are important controls over the abundance of diagenetic features. 相似文献
20.
显生宙非骨屑碳酸盐矿物经历了文石海和方解石海的交替,主要造礁生物和沉积物生产者的骨骼矿物与非骨屑碳酸盐矿物具有同步变化的趋势。这种长期的变化趋势可以用海水化学Mg/Ca摩尔比的变化来解释。流体包裹体、同位素和微量元素等证据也证实了海水化学在地质历史中经历过剧烈的变化。虽然生物诱导矿化和生物控制矿化的相对重要性一直存在争议,但古生物地层记录和人工海水养殖实验结果都表明,海水化学演化对生物矿化有重要的影响,体现在造礁生物群落的兴衰、生物起源时对骨骼矿物类型的选择以及微生物碳酸盐岩在地质历史中的分布等。这些为研究前寒武纪海水化学演化、古气候和古环境的重建、同位素地层对比以及碳酸盐的沉积和成岩等问题提供了新的思路。 相似文献