首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 30 毫秒
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   

2.
The seeded precipitation (crystal growth) of aragonite and calcite from sea water, magnesium-depleted sea water, and magnesium-free sea water has been studied by means of the steady-state disequilibrium initial rate method. Dissolved magnesium at sea water levels appears to have no effect on the rate of crystal growth of aragonite, but a strong retarding effect on that of calcite. By contrast, at levels less than about 5 per cent of the sea water level, Mg has little or no effect on calcite growth. Extended crystal growth on pure calcite seeds in sea water of normal Mg content resulted in the crystallization of magnesium calcite overgrowths, containing 7–10 mole % MgCO3 in solid solution. This suggests that the rate inhibition by Mg is due to its incorporation within the calcite crystal structure during growth, which causes the resulting magnesian calcite to be considerably more soluble than pure calcite. The standard free energy of formation of 8.5 mole% Mg calcite calculated on this assumption is in good agreement with independent estimates of magnesian calcite stability.From the work of Katz (Geochim. Cosmochim. Acta37, 1563–1586, 1973), Plummer and Mackenzie (Amer. J. Sci. 273, 515–522, 1974), and the present paper, it can be predicted that the most stable calcite in Ca-Mg exchange equilibrium with sea water contains between 2 and 7 mole%MgCO3 in solid solution. Likewise, calcites containing more than 8.5 mole% MgCO3 are less stable, and those containing less than 8.5 mole% MgCO3 are more stable than aragonite plus Ca and Mg in sea water.  相似文献   

3.
Transient aragonite seas occurred in the early Cambrian but several models suggest the late Cambrian was a time of calcite seas. Here, evidence is presented from the Andam Group, Huqf High, Oman (Gondwana) that suggests a transient Furongian (late Cambrian) aragonite sea, characterized by the precipitation of aragonite and high‐Mg calcite ooids and aragonite isopachous, fibrous, cements. Stable carbon isotope data suggest that precipitation occurred just before and during the SPICE (Steptoean Positive Carbonate Isotope Excursion). Aragonite and high‐Mg calcite precipitation can be accounted for if mMg:Ca ratios were around 1.2 given the very high atmospheric CO2 at that time and if precipitation occurred in warm waters associated with the SPICE. This, together with reported occurrences of early Furongian aragonite ooids from various locations in North America (Laurentia), suggests that aragonite and high‐Mg calcite precipitation from seawater may have been more than just a local phenomenon.  相似文献   

4.
The most ubiquitous syn-sedimentary cements affecting Mururoa atoll are composed of magnesian calcite. Three main types are distinguished: fibrous, bladed and sparitic on the basis of petrography, morphology and MgCO3 concentration of the constituting crystals, while peloid infills, a particular form of HMC chemical precipitation, also exist. Petrographic evidence and isotopic signatures are compatible with marine precipitation. Mururoa atoll was exposed several times to meteoric diagenesis resulting in varied diagenetic alterations including selective dissolution and partial dolomitization of Mg-calcite cements. These alterations are responsible for substantial modifications of the initial cement fabrics and may introduce unconformities in the diagenetic chronology. The first stage of the partial dissolution of Mg-calcite induces the development of chalky, white friable zones within the initially crystalline, hard cement layers. At ultrascale, this is due to the creation of micro-voids along the elongate cement fibres. Advanced dissolution includes total disappearance of cement portions as attested to by large voids within the cement crust and/or between superposed cement layers. Mg-calcite dissolution is related to meteoric diagenesis during periods of Quaternary exposure. The creation of voids within Mg-calcite layers is due to the mechanical removal of previously altered calcium carbonate, a process suggesting marine or non-marine water flow, probably in the vadose environment. Selective dolomitization of Mururoa cements involves alternations of calcite and dolomite which form successive cement-like rinds within primary cavities. At Mururoa, these alternations are the result of selective dolomitization of the pre-existing Mg-calcite cements rather than successive precipitation of calcite and dolomite. Selective dolomitization of Mg-calcite cements at Mururoa indicates that a given cement succession is not necessarily a simple chronological sequence. Oxygen isotope values of dolomites are enriched in δ186 by about 3‰ PDB within calcite-dolomite pseudo-alternations. The dolomitizing fluid at Mururoa seems similar to present marine water although some mixture with meteoric water is probable to favour dissolution associated with dolomitization.  相似文献   

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

6.
Stoichiometric solubility constants of calcite in initially supersaturated solutions of various magnesium to calcium concentration ratios but identical ionic strength were determined at 25°C and one atmosphere total pressure.The thermodynamic solubility constant of calcite is used with ion pairing equations to interpret the data reported in this study. Results indicate that even though magnesian calcites, rather than pure calcite, precipitate from seawater solutions containing magnesium ions, the incorporation of MgCO3 in the calcite crystal lattice does not extensively alter the equilibrium calcium carbonate activity product.The equilibrium activity of the ionic species in solution and the composition of magnesian calcite overgrowths precipitated from solutions of similar composition are used to calculate the solubility of magnesian calcites. The values for magnesian calcite solubilities obtained by this approach are lower than those obtained from the dissolution kinetics of biogenic carbonates.  相似文献   

7.
Lower Cretaceous (Hauterivian) bioclastic sandstone turbidites in the Scapa Member (North Sea Basin) were extensively cemented by low-Mg calcite spars, initially as rim cements and subsequently as concretions. Five petrographically distinct cement stages form a consistent paragenetic sequence across the Scapa Field. The dominant and pervasive second cement stage accounts for the majority of concretions, and is the focus of this study. Stable-isotope characterization of the cement is hampered by the presence of calcitic bioclasts and of later cements in sponge spicule moulds throughout the concretions. Nevertheless, trends from whole-rock data, augmented by cement separates from synlithification fractures, indicate an early calcite δ18O value of+0·5 to -1·5‰ PDB. As such, the calcite probably precipitated from marine pore fluids shortly after turbidite deposition. Carbon isotopes (δ13C=0 to -2‰ PDB) and petrographic data indicate that calcite formed as a consequence of bioclastic aragonite dissolution. Textural integrity of calcitic nannoplankton in the sandstones demonstrates that pore fluids remained at or above calcite saturation, as expected for a mineral-controlled transformation. Electron probe microanalyses demonstrate that early calcite cement contains <2 mol% MgCO3, despite its marine parentage. Production of this cement is ascribed to a combination of an elevated aragonite saturation depth and a lowered marine Mg2+/Ca2+ ratio in early Cretaceous ‘calcite seas’, relative to modern oceans. Scapa cement compositions concur with published models in suggesting that Hauterivian ocean water had a Mg2+/Ca2+ ratio of ≤1. This is also supported by consideration of the spatial distribution of early calcite cement in terms of concretion growth kinetics. In contrast to the dominant early cement, late-stage ferroan, 18O-depleted calcites were sourced outwith the Scapa Member and precipitated after 1–2 km of burial. Our results emphasize that bioclast dissolution and low-Mg calcite cementation in sandstone reservoirs should not automatically be regarded as evidence for uplift and meteoric diagenesis.  相似文献   

8.
海水化学演化对生物矿化的影响综述   总被引：1，自引：1，他引：0       下载免费PDF全文
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   

9.
Previous studies on early submarine diagenesis of periplatform carbonates have implied that these originally polymineralic (aragonite, magnesian calcite, calcite) sediments are susceptible to early diagenesis only in current-swept open seaways or where surficially exposed by erosion on the seafloor. It has also been proposed that while in the shallow subsurface, periplatform oozes retain their original mineralogy for at least 200,000–400,000 yr and remain unlithified for tens of millions of years. Evidence is reported here for extensive calcitization and selective lithification of periplatform oozes of late Pleistocene age in two piston cores collected from water depths of ～ 1,000 m north of Little Bahama Bank. It is shown that shallow (<30 m) subsurface diagenesis can significantly alter the original mineralogy of periplatform oozes to predominantly calcite in less than 440,000 yr, and that cementation by calcite can produce chalk-ooze sequences within the same time-frame. Periplatform oozes that originally contain a high percentage of bank-derived magnesian calcite appear to have a higher diagenetic potential than those originally low in magnesian calcite. Shallow subsurface calcitization and fithification greatly reduce the diagenetic potential of periplatform carbonates, and chalk-ooze sequences apparently can persist for tens of millions of years and to burial depths of at least 300 m. Shallow subsurface diagenesis, at water depths > 1,000 m, proceeds via dissolution of magnesian calcite and aragonite and reprecipitation of calcite as allochem fillings, exterior overgrowths and cement. It is speculated that density-driven ‘Kohout convection‘, where seawaters under-saturated with respect to magnesian calcite and aragonite and saturated/supersaturated with respect to calcite flow through the margins of carbonate platforms, is the primary driving mechanism for shallow subsurface diagenesis. Removal of Mg during early stages of deep seafloor and shallow subsurface diagenesis should increase the Mg content of interstitial waters which is likely to increase the ‘dolomitizing potential’ of Kohout convection fluid flow.  相似文献   

10.
The uplifted Pleistocene terraces along the coast of southern Sinai exhibit a well developed reef system formed during isotope stage 9, and a younger one formed during isotope stage 5. An intermediate reef corresponding to isotope stage 7 occurs only as an erosional relic in the study area. The sediments comprise reefal framestones, peri-reefal facies, coral rubble, and siliciclastic-dominated beach and aeolian facies. The compositional and textural complexity of the sediments leads to a highly variable spatial distribution of diagenetic features. However, the geometric relationships and elemental analyses allow a reconstruction of the general diagenetic evolution: during the major eustatic sea-level highstand of isotope stage 9, the Older Reef was constructed and cemented with aragonite and high-Mg calcite. Climate was probably semiarid with some rainy periods which permitted the installation of ephemeral freshwater lenses, especially during the minor sea-level lowstand within isotope stage 9. In these lenses, and during the subsequent major sea-level lowstand, some freshwater dissolution occurred. The highstand during isotope stage 7 led to the construction of the Intermediate Reef. In the Older Reef, some high-Mg calcite precipitated at that time. Dolomite cement formed either in marine interstitial waters modified by some freshwater input, or in a hypersaline context. Phreatic-meteoric low-Mg calcite cement covers, and partly replaces, previous marine cements and dolomite, but is still attributed to the major highstand of isotope stage 7 when freshwater lenses could develop during minor sea-level lowstands. The subsequent major sea-level lowstand was dominated by an arid climate, and only a little freshwater corrosion occurred. The Younger Reef formed during the major highstand of isotope stage 5. Aragonite and high-Mg calcite cements, as well as some dolomite, are common within the reef, whereas freshwater cements are limited to beach and aeolian facies. Due to tectonic uplift, only the lower part of the Older Reef was reflooded during isotope stage 5, and only some aragonite crystals precipitated on top of dolomite or low-Mg calcite. The interrelationships between tectonics, sea-level variations of different orders, and climatic changes thus had a profound impact on the diagenetic history of these reef systems.  相似文献   

11.
In this study, the stable isotope and trace element geochemistries of meteoric cements in Pleistocene limestones from Enewetak Atoll (western Pacific Ocean), Cat Island (Bahamas), and Yucatan were characterized to help interpret similar cements in ancient rocks. Meteoric calcite cements have a narrow range of δ18O values and a broad range of δ13C values in each geographical province. These Pleistocene cements were precipitated from water with stable oxygen isotopic compositions similar to modern rainwater in each location. Enewetak calcite cements have a mean δ18O composition of ?6.5%0 (PDB) and δ13C values ranging from ?9.6 to +0.4%0 (PDB). Sparry calcite cements from Cat Island have a mean δ18O composition of ?4.1%0 and δ13C values ranging from ?6.3 to + 1.1%0. Sparry cements from Yucatan have a mean δ18O composition of ?5.7%0 and δ13C values of ?8.0 to ?2.7%0. The mean δ18O values of these Pleistocene meteoric calcite cements vary by 2.4%0 due to climatic variations not related directly to latitude. The δ13C compositions of meteoric cements are distinctly lower than those of the depositional sediments. Variations in δ13C are not simply a function of distance below an exposure surface. Meteoric phreatic cements often have δ13C compositions of less than —4.0%0, which suggests that soil-derived CO2 and organic material were washed into the water table penecontemporaneous with precipitation of phreatic cements. Concentrations of strontium and magnesium are quite variable within and between the three geographical provinces. Mean strontium concentrations for sparry calcite cements are, for Enewetak Atoll, 620 ppm (σ= 510 ppm); for Cat Island, 1200 ppm (σ= 980 ppm); and for Yucatan, 700 ppm (σ= 390 ppm). Equant cements, intraskeletal cements, and Bahamian cements have higher mean strontium concentrations than other cements. Equant and intraskeletal cements probably precipitated in more closed or stagnant aqueous environments. Bahamian depositional sediments had higher strontium concentrations which probably caused high strontium concentrations in their cements. Magnesium concentrations in Pleistocene meteoric cements are similar in samples from Enewetak Atoll (mean =1.00 mol% MgCO3; σ= 0.60 mol% MgCO3) and Cat Island (mean = 0.84 mol% MgCO3; σ= 0.52mol% MgCO3) but Yucatan samples have higher magnesium concentrations (mean = 2.20 mol% MgCO3: σ= 0.84mol% MgCO3). Higher magnesium concentrations in some Yucatan cements probably reflect precipitation in environments where sea water mixed with fresh water.  相似文献   

12.
Equilibrium constants at stoichiometric saturation with respect to various magnesian calcite compositions were measured using free-drift dissolution rate data and inverse time plots to estimate equilibrium pH. The equilibrium constants determined for two ultrasonically cleaned and annealed biogenic magnesian calcites (12 and 18 mole % MgCO3) in CaCl2 + MgCl2 media at two Mg:Ca molar ratios (1:5 and 5:1) are about three times smaller than those previously reported by Plummer and Mackenzie (1974). These equilibrium constants are not affected by changes in initial pH value, solid:solution ratio, or solution Mg:Ca molar ratio when the ion activity product is expressed in the fractional exponent form. Other models for expression of the equilibrium ion activity product fail to yield consistent values in solutions of different Mg:Ca molar ratios.Experiments performed using crushed samples not ultrasonically cleaned and annealed yield equilibrium constants which vary with solid:solution ratio. Those performed at high solid:solution ratios yield values which approach those previously reported. Submicron size particles and crystal strain induced by crushing the biogenic carbonates may cause more rapid dissolution rates and, hence, overestimation of the solubility of samples not prepared so as to minimize these effects. Thus, the large range in reported solubilities of magnesium calcites may be a result of differences in sample preparation procedure.The results of these measurements shift the thermodynamic equivalence point of aragonite and magnesian calcite from 7.5 mole % MgCO3 up to 12 mole % MgCO3 and prompt a reassessment of models for carbonate diagenetic reactions in natural environments.  相似文献   

13.
Large areas of southern Australia and New Zealand are covered by mid‐Tertiary limestones formed in cool‐water, shelf environments. The generally destructive character of sea‐floor diagenesis in such settings precludes ubiquitous inorganic precipitation of carbonates, yet these limestones include occasional units with marine cements: (1) within rare in situ biomounds; (2) within some stacked, cross‐bedded sand bodies; (3) at the top of metre‐scale, subtidal, carbonate cycles; and (4) most commonly, associated with certain unconformities. The marine cements are dominated by isopachous rinds of fibrous to bladed spar, interstitial homogeneous micrite and interstitial micropeloidal micrite, often precipitated sequentially in that order. Internal sedimentation of microbioclastic micrite may occur at any stage. The paradox of marine‐cemented limestone units in an overall destructive cool‐water diagenetic regime may be explained by the precipitation of cement as intermediate Mg‐calcite from marine waters undersaturated with respect to aragonite. In some of the marine‐cemented limestones, aragonite biomoulds may include marine cement/sediment internally, suggesting that dissolution of aragonite can at times be wholly marine and not always involve meteoric influences. We suggest that marine cementation occurred preferentially, but not exclusively, during periods of relatively lowered sea level, probably glacio‐eustatically driven in the mid‐Tertiary. At times of reduced sea level, there was a relative increase in both the temperature and the carbonate saturation state of the shelf waters, and the locus of carbonate sedimentation shifted towards formerly deeper shelf sites, which now experienced increased swell wave and/or tidal energy levels, fostering sediment abrasion and reworking, reduced sedimentation rates and freer exchange of sediment pore‐waters. Energy levels were probably also enhanced by increased upwelling of cold, deep waters onto the Southern Ocean margins of the Australasian carbonate platforms, where water‐mass mixing, warming and loss of CO2 locally maintained critical levels of carbonate saturation for sea‐floor cement precipitation and promoted the phosphate‐glauconite mineralization associated with some of the marine‐cemented limestone units.  相似文献   

14.
西沙群岛现代海滩岩岩石学初见   总被引：3，自引：0，他引：3       下载免费PDF全文
引言我国美丽富饶的西沙群岛位于海南岛东南180海里南海西北部台阶式大陆坡的西沙台阶之上,由近40个岛洲礁滩组成。其中岛屿部分,除高尖石是由火山岩构成的以外,其余均为珊瑚礁岛屿。  相似文献   

15.
Magnesian calcite is an important sedimentary component in the deep-sea sediments of the eastern Mediterranean Sea, comprising an average of 20–50% of the carbonate fraction in most areas. The lack of any obvious biogenic source, plus similarities with magnesian-rich lutites from the Red Sea and deep-sea cements from other areas suggest that this magnesian calcite was precipitated inorganically. Although the exact mode of precipitation is not understood at present, it probably occurred at the water-sediment interface under elevated salinity and temperature conditions, such as those present in the modern eastern Mediterranean. Precipitation did not occur during periods of lower temperatures and/or salinities such as during the stagnant conditions caused by the influx of fresh waters from melting Pleistocene glaciers. The eastern Mediterranean magnesium-rich sediments appear to represent an intermediate stage between normal deep-sea sediments and those from the warm hpyersaline Red Sea. Normal deep-sea carbonates are composed almost entirely of biogenic calcite, whereas the Red Sea magnesian calcite alternates with layers of aragonite that were precipitated under elevated salinity and temperature conditions brought about by lowered stands of sea level.  相似文献   

16.
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   

17.
Petrography demonstrates the presence of three types of fibrous calcite cement in buildup deposits of the Kullsberg Limestone (middle Caradoc), central Sweden. Translucent fibrous calcite has intrinsic blue luminescence (CL) indicative of pure calcite. This cement has 2–5 mol% MgCO3, low Mn and Fe (≤ 100 p.p.m.), and is considered to be slightly altered to unaltered, primary low- to intermediate-Mg calcite. Grey turbid fibrous calcite has variable but generally low MgCO3 content (most analyses <2 mol%) and variable CL response, with Mn and Fe concentrations up to 1200 and 500 p.p.m., respectively. The heterogeneous characteristics of this variety of fibrous calcite are caused by diagenetic alteration of a translucent fibrous calcite precursor. Light-brown turbid fibrous calcite has low MgCO3 (near 1 mol%) and variable Mn (up to 800 p.p.m.) and Fe (up to 500 p.p.m.) concentrations, with an abundance of bright luminescent patches, which formed during alteration caused by reducing diagenetic fluids. The δ13C and δ18O values of all fibrous calcite form a tight field (δ13C=1·7 to 3·1‰ PDB, δ18O= ? 2·6 to ? 4·1‰ PDB) compared with fibrous calcite isotope values from other units. Fibrous calcite δ18O values are larger than adjacent meteoric or burial cements, which have δ18O δ ? 8‰ PDB. Consequently, most diagenetic alteration of Kullsberg fibrous calcite is interpreted to have occurred in the marine diagenetic realm. First-generation equant and bladed calcite cements, which pre-date fibrous calcite, are interpreted as unaltered, low-Mg calcite marine cements based on δ13C and δ18O data (δ13C = 2·3 to 2·7‰ PDB, δ18O= ? 2·8 to ? 3·5‰ PDB). Unlike fibrous cement, which reflects global sea water chemistry, first-generation equant and bladed calcite are indicators of localized modification of seawater chemistry in restricted settings. Kullsberg abiotic marine cements have larger δ18O values than most Caradoc marine precipitates from equatorial Laurentia. Positive Kullsberg δ18O values are attributed to lower seawater temperatures and/or slightly elevated salinity on the Baltic platform relative to seawater from which other marine precipitates formed.  相似文献   

18.
祝仲蓉 Marsh.  J 《沉积学报》1992,10(1):133-145
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   

19.
The Albian-Danian limestones of Cauvery Basin show a wide range of d13C and d18O values (–13.2 to +1.1% and –9.0 to –2.5%, respectively). The cement samples show negative carbon and oxygen isotope values (–18.9 to –3.9% and –9.0 to –4.3%, respectively). The petrographic study reveals the presence of algae, molluscs, bryozoans, foraminifers and ostracods as major framework constituents. The limestones have microspar and equant sparry calcite cements. The pore spaces and vugs are filled with sparry calcite cement. The bivariate plot of d13C and d18O suggests that most of the samples fall in the freshwater limestone and meteoric field, while few samples fall in the marine limestone and soil calcite fields. The presence of sparry calcite cement, together with negative carbon and oxygen isotope values, indicates that these limestones have undergone meteoric diagenesis.  相似文献   

20.
Oolitic sediments occur over large portions of the outer continental shelf off northernmost Brazil and southern French Guiana. Carbon-14 dates, stable isotope values and analogies with similar deposits from other areas in the world indicate that the ooids were formed in shallow water (possibly protected hypersaline environments) during low stands of sea level. In contrast to both modern ooids and other relict ooids, however, the Amazon shelf ooids are composed entirely of magnesian calcite (12 mol % MgCO3) and possess radial crystal microstructures. A comparison of water depths and ages of the Amazon ooids with the generally accepted eustatic sea level curve indicates that the Amazon shelf subsided more than 100 m 16-21 thousand years ago. Prior to and subsequent to the subsidence, however, the outer shelf remained relatively stable.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号