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1.
Compaction and associated fluid flow are fundamental processes in sedimentary basin deformation. Purely mechanical compaction originates mainly from pore fluid expulsion and rearrangement of solid particles during burial, while chemo‐mechanical compaction results from Intergranular Pressure‐Solution (IPS) and represents a major mechanism of deformation in sedimentary basins during diagenesis. The aim of the present contribution is to provide a comprehensive 3D framework for constitutive and numerical modeling of purely mechanical and chemo‐mechanical compaction in sedimentary basins. Extending the concepts that have been previously proposed for the modeling of purely mechanical compaction in finite poroplasticity, deformation by IPS is addressed herein by means of additional viscoplastic terms in the state equations of the porous material. The finite element model integrates the poroplastic and poroviscoplastic components of deformation at large strains. The corresponding implementation allows for numerical simulation of sediments accretion/erosion periods by progressive activation/deactivation of the gravity forces within a fictitious closed material system. Validation of the numerical approach is assessed by means of comparison with closed‐form solutions derived in the context of a simplified compaction model. The last part of the paper presents the results of numerical basin simulation performed in one dimensional setting, demonstrating the ability of the modeling to capture the main features in elastoplastic and viscoplastic compaction. Copyright © 2016 John Wiley & Sons, Ltd.  相似文献   

2.
大港滩海区第三系湖相混积岩的成因与成岩作用特征   总被引：13，自引：7，他引：13  
马艳萍  刘立 《沉积学报》2003,21(4):607-614
大港滩海第三系沙河街组一段下部分布的混积岩主要为陆源碎屑质-碳酸盐混积岩, 其次为碳酸盐质-陆源碎屑混积岩和含碳酸盐-陆源碎屑混积岩.其中白水头地区的混积岩发育于辫状河-扇三角洲前缘水下分流河道沉积体系之中,为相缘渐变混合沉积的产物;而马东-马东东地区的混积岩发育于重力流沉积体系之中,为浊流沉积的产物.本区混积岩主要经历了压实作用、胶结作用和溶蚀溶解作用.孔隙流体的化学性质经历了由碱性到酸性,最后又回到碱性的变化历程.其中海绿石、微晶方解石、部分石英溶蚀和连生方解石为碱性流体条件下的共生组合;次生加大石英、油气侵位、溶蚀溶解、高岭石为酸性条件下的共生组合;伊利石、绿泥石、钠长石化、孔隙充填方解石和白云石为碱性流体条件下的共生组合.  相似文献   

3.
The calcium isotopic compositions (δ44Ca) of 30 high-purity nannofossil ooze and chalk and 7 pore fluid samples from ODP Site 807A (Ontong Java Plateau) are used in conjunction with numerical models to determine the equilibrium calcium isotope fractionation factor (αs−f) between calcite and dissolved Ca2+ and the rates of post-depositional recrystallization in deep sea carbonate ooze. The value of αs−f at equilibrium in the marine sedimentary section is 1.0000 ± 0.0001, which is significantly different from the value (0.9987 ± 0.0002) found in laboratory experiments of calcite precipitation and in the formation of biogenic calcite in the surface ocean. We hypothesize that this fractionation factor is relevant to calcite precipitation in any system at equilibrium and that this equilibrium fractionation factor has implications for the mechanisms responsible for Ca isotope fractionation during calcite precipitation. We describe a steady state model that offers a unified framework for explaining Ca isotope fractionation across the observed precipitation rate range of ∼14 orders of magnitude. The model attributes Ca isotope fractionation to the relative balance between the attachment and detachment fluxes at the calcite crystal surface. This model represents our hypothesis for the mechanism responsible for isotope fractionation during calcite precipitation. The Ca isotope data provide evidence that the bulk rate of calcite recrystallization in freshly-deposited carbonate ooze is 30-40%/Myr, and decreases with age to about 2%/Myr in 2-3 million year old sediment. The recrystallization rates determined from Ca isotopes for Pleistocene sediments are higher than those previously inferred from pore fluid Sr concentration and are consistent with rates derived for Late Pleistocene siliciclastic sediments using uranium isotopes. Combining our results for the equilibrium fractionation factor and recrystallization rates, we evaluate the effect of diagenesis on the Ca isotopic composition of marine carbonates at Site 807A. Since calcite precipitation rates in the sedimentary column are many orders of magnitude slower than laboratory experiments and the pore fluids are only slightly oversaturated with respect to calcite, the isotopic composition of diagenetic calcite is likely to reflect equilibrium precipitation. Accordingly, diagenesis produces a maximum shift in δ44Ca of +0.15‰ for Site 807A sediments but will have a larger impact where sedimentation rates are low, seawater circulates through the sediment pile, or there are prolonged depositional hiatuses.  相似文献   

4.
Septarian concretions occur at several horizons within the Oxford Clay Formation, a marine mudstone containing pristine aragonite and immature biomarker molecules. They record the passage of at least four generations of pore fluids, the first of marine origin and the last still present in cavities. Concretion bodies formed, cracked, and calcite and pyrite precipitated in and around the cracks within the sulphate reduction zone, as demonstrated by C, O, S and Sr isotopic composition (Pore fluid 1). Before major compaction, sandstone dykes were intruded locally, and baryte precipitated, followed by coarse calcite cements with isotopically light oxygen and radiogenic strontium, indicating the introduction of meteoric-derived water (Pore fluid 2). Later, coarse celestine within concretions has distinct sulphur-isotopic composition and requires a further, geographically restricted, water source (Pore fluid 3). Celestine-bearing concretions contain water in tight cavities whose isotopic composition is close to that of modern precipitation. Its chemistry shows that it is equilibrating with pre-existing minerals implying a relatively recent origin (Pore fluid 4). The mineralogy of the Oxford Clay concretions shows that complex results can follow from a simple burial and uplift history, and that multiple generations of pore fluids can pass through a low-permeability clay.  相似文献   

5.
准噶尔盆地西北缘克拉玛依—百口泉地区侏罗系砂岩、砂砾岩储层经历了压实、胶结、溶蚀等多种成岩作用,其中压实和溶蚀作用是控制储层物性的主要成岩作用,其次为胶结作用。压实作用以机械压实为主,是孔隙减少的主要原因。胶结作用主要为碳酸盐胶结,少量黄铁矿胶结,偶见方沸石胶结和硅质胶结。溶蚀作用导致碳酸盐胶结物、长石颗粒和少量岩屑溶解流失。储层孔隙经历了由原生到次生的演化过程。在成岩演化过程中,长石的溶蚀作用、碳酸盐矿物的沉淀与溶解作用是影响储层孔隙发育的关键因素,早期方解石的胶结有利于后期次生孔隙的形成。在克-乌断裂带上、下盘地层中,断裂带上盘埋深浅,一般小于1200m,原生孔隙非常发育;断裂带下盘埋深较深,压实作用强,原生孔隙所占比例明显减少,次生溶蚀孔隙相对发育。次生孔隙的形成受流体及断裂控制。  相似文献   

6.
Pore fluid calcium isotope, calcium concentration and strontium concentration data are used to measure the rates of diagenetic dissolution and precipitation of calcite in deep-sea sediments containing abundant clay and organic material. This type of study of deep-sea sediment diagenesis provides unique information about the ultra-slow chemical reactions that occur in natural marine sediments that affect global geochemical cycles and the preservation of paleo-environmental information in carbonate fossils. For this study, calcium isotope ratios (δ44/40Ca) of pore fluid calcium from Ocean Drilling Program (ODP) Sites 984 (North Atlantic) and 1082 (off the coast of West Africa) were measured to augment available pore fluid measurements of calcium and strontium concentration. Both study sites have high sedimentation rates and support quantitative sulfate reduction, methanogenesis and anaerobic methane oxidation. The pattern of change of δ44/40Ca of pore fluid calcium versus depth at Sites 984 and 1082 differs markedly from that of previously studied deep-sea Sites like 590B and 807, which are composed of nearly pure carbonate sediment. In the 984 and 1082 pore fluids, δ44/40Ca remains elevated near seawater values deep in the sediments, rather than shifting rapidly toward the δ44/40Ca of carbonate solids. This observation indicates that the rate of calcite dissolution is far lower than at previously studied carbonate-rich sites. The data are fit using a numerical model, as well as more approximate analytical models, to estimate the rates of carbonate dissolution and precipitation and the relationship of these rates to the abundance of clay and organic material. Our models give mutually consistent results and indicate that calcite dissolution rates at Sites 984 and 1082 are roughly two orders of magnitude lower than at previously studied carbonate-rich sites, and the rate correlates with the abundance of clay. Our calculated rates are conservative for these sites (the actual rates could be significantly slower) because other processes that impact the calcium isotope composition of sedimentary pore fluid have not been included. The results provide direct geochemical evidence for the anecdotal observation that the best-preserved carbonate fossils are often found in clay or organic-rich sedimentary horizons. The results also suggest that the presence of clay minerals has a strong passivating effect on the surfaces of biogenic carbonate minerals, slowing dissolution dramatically even in relation to the already-slow rates typical of carbonate-rich sediments.  相似文献   

7.
The sedimentology, mineralogy and pore fluid chemistry of seven cores from the Holocene sediments of Florida Bay were studied to determine the physical processes and diagenetic reactions affecting the sediments. The cores were taken in a transect from a shallow mudbank onto a small adjacent island, Jimmy Key. Steady state models of pore fluid chemistry are used to estimate the rates of various reactions. In the mudbank sediments, little carbonate mineral diagenesis is taking place. No change in sediment mineralogy is detectable and pore water profiles of Ca2+, Mg2+ and Sr2+ show only minor variation. Chloride concentrations indicate substantial biological mixing of seawater from the bay into the sediments in one of the cores. Pore water analyses of sulphate and alkalinity show only a low degree of sulphate depletion and a decreasing extent of sulphate reduction downcore. Models of sulphate reduction in the mudbank show that there is substantial chemical exchange between the sediment pore fluids and water from the bay probably as a result of bio-irrigation. The sulphate and alkalinity data also suggest that the underlying Pleistocene rocks contain water of near normal seawater composition. Stratigraphic analysis and δ13C analyses of the organic carbon in the sediments of the island cores show that the sediments were primarily deposited in a subtidal mudbank setting; only the upper 20–30 cm is supratidal in origin. Nevertheless, island formation had a significant effect on pore fluid chemistry and the types of diagenetic reactions throughout the sediment column. Chloride in the sediment pore fluids is more than twice the normal seawater concentrations over most of the depth of the cores. The constant, elevated chloride concentrations indicate that hypersaline fluids which formed in ponds on the island are advected downward through the sediments. Models of the chloride profiles yield an estimate of 2·5 cm yr?1 as a minimum advective velocity. Changes in pore water chemistry with depth are interpreted as indicating the following sequence of reactions: (1) minor high-Mg calcite dissolution and low-Mg calcite precipitation, from 0 to 35 cm; (2) Ca- or Mg-sulphate dissolution and low-Mg calcite precipitation, from 5 to 35 cm; (3) dolomite or magnesite precipitation together with sulphate reduction, from 35 to 55 cm; and (4) little reaction below 55 cm. In addition, one or more as yet unidentified reactions must be taking place from 5 to 55 cm depth as an imbalance in possible sources and sinks of alkalinity is observed. The imbalance could be explained if chloride is not completely conservative. Despite the pore fluid chemical evidence for diagenetic reactions involving carbonate minerals, no changes in sediment mineralogy were detected in X-ray diffraction analyses, probably because of the comparatively young age of the island.  相似文献   

8.
The 87Sr/86Sr ratios and Sr concentrations in sediment and pore fluids are used to evaluate the rates of calcite recrystallization at ODP Site 807A on the Ontong Java Plateau, an 800-meter thick section of carbonate ooze and chalk. A numerical model is used to evaluate the pore fluid chemistry and Sr isotopes in an accumulating section. The deduced calcite recrystallization rate is 2% per million years (%/Myr) near the top of the section and decreases systematically in older parts of the section such that the rate is close to 0.1/age (in years). The deduced recrystallization rates have important implications for the interpretation of Ca and Mg concentration profiles in the pore fluids. The effect of calcite recrystallization on pore fluid chemistry is described by the reaction length, L, which varies by element, and depends on the concentration in pore fluid and solid. When L is small compared to the thickness of the sedimentary section, the pore fluid concentration is controlled by equilibrium or steady-state exchange with the solid phase, except within a distance L of the sediment-water interface. When L is large relative to the thickness of sediment, the pore fluid concentration is mostly controlled by the boundary conditions and diffusion. The values of L for Ca, Sr, and Mg are of order 15, 150, and 1500 meters, respectively. LSr is derived from isotopic data and modeling, and allows us to infer the values of LCa and LMg. The small value for LCa indicates that pore fluid Ca concentrations, which gradually increase down section, must be equilibrium values that are maintained by solution-precipitation exchange with calcite and do not reflect Ca sources within or below the sediment column. The pore fluid Ca measurements and measured alkalinity allow us to calculate the in situ pH in the pore fluids, which decreases from 7.6 near the sediment-water interface to 7.1 ± 0.1 at 400-800 mbsf. While the calculated pH values are in agreement with some of the values measured during ODP Leg 130, most of the measurements are artifacts. The large value for LMg indicates that the pore fluid Mg concentrations at 807A are not controlled by calcite-fluid equilibrium but instead are determined by the changing Mg concentration of seawater during deposition, modified by aqueous diffusion in the pore fluids. We use the pore fluid Mg concentration profile at Site 807A to retrieve a global record for seawater Mg over the past 35 Myr, which shows that seawater Mg has increased rapidly over the past 10 Myr, rather than gradually over the past 60 Myr. This observation suggests that the Cenozoic rise in seawater Mg is controlled by continental weathering inputs rather than by exchange with oceanic crust. The relationship determined between reaction rate and age in silicates and carbonates is strikingly similar, which suggests that reaction affinity is not the primary determinant of silicate dissolution rates in nature.  相似文献   

9.
We present a 2D numerical model for the growth of calcite from supersaturated aqueous solutions under laminar, open-channel flow conditions. The model couples solution chemistry, precipitation at solution/calcite interfaces, hydrodynamics, diffusion and degassing. The model output is compared with experimental results obtained using an oversaturated calcite solution produced by mixing CaCl2 and Na2CO3. The precipitation rate is observed to increase when the supersaturated solution flows over an obstruction, leading to a growth instability that causes the formation of terraces. At relatively high flow rates, the most important mechanism for this behaviour seems to be hydrodynamic advection of dissolved species either towards or away from the calcite surface, depending on location relative to the obstruction, which deforms the concentration gradients. At lower flow rates, steepening of diffusion gradients around protrusions becomes important. Enhanced degassing over the obstruction due to shallowing and pressure drop is not important on small scales. Diffusion controlled transport close to the calcite surface can lead to a fingering-type growth instability, which generates porous textures. Our results are consistent with existing diffusive boundary layer theory, but for flow over non-smooth surfaces, simple calcite precipitation models that include empirical correlations between fluid flow rate and calcite precipitation rate are inaccurate.  相似文献   

10.
The evolution of fluid chemistry in compacting rock is controlled by coupled chemical processes and rock deformation. In order to characterize this evolution, we conducted water-rock interaction experiments using quartz aggregates at 150 °C and effective pressure of 34.5 MPa. A coupled fluid flow, chemical reaction, and creep compaction model is developed, in which both free-surface reaction and grain-contact dissolution are considered as system volume and porosity evolve.The direct experimental measurement and numerical modeling indicate that effective pressure has significant effects on pore-fluid chemistry. At the early stages of compaction, pore fluids are supersaturated with respect to bulk quartz. With increasing compaction and time, solute concentrations gradually decrease to saturated conditions. Supersaturation is caused mainly by dissolution of ultrafines and high-energy, unstable surfaces which are produced by stress concentrations at grain contacts during the very early stages of compaction. Grain-contact dissolution also contributes to the solute increase in pore fluid in the early stage of compaction, but the effect is small compared to that of ultrafines and unstable surfaces and only slight supersaturation can be produced by it. The gradual decrease in pore-fluid concentration is related to the mechanical removal of ultrafines by pore-fluid flow and the dissolution of ultrafines and unstable surfaces. It also results from the lessening of grain-contact dissolution.Pore fluids in compacting sedimentary basins of quartz sandstone are nearly saturated throughout most of diagenetic processes. Ultrafines and unstable surfaces produced by stress appear not to be the major sources of quartz cement.  相似文献   

11.
济阳坳陷古近系成岩作用及其对储层质量的影响?   总被引：12，自引：5，他引：12  
大量的储层分析化验资料研究表明，济阳坳陷古近系砂岩储层经历了压实、胶结等多种成岩作用。压实作用以机械压实为主，压溶作用较少。胶结作用主要有十分普遍的石英次生加大胶结、碳酸盐胶结、粘土矿物胶结。碳酸盐胶结物有早、晚两期，早期泥晶方解石主要分布在浅层，连晶方解石充填的深度分布范围大，中深部最为发育。溶蚀作用主要有碳酸盐胶结物、长石颗粒和少量岩屑溶蚀。储层孔隙经历了由原生到次生的演化过程，在成岩演化过程中，长石的溶蚀作用、碳酸盐矿物的沉淀与溶解作用是影响孔隙大小的关键因素，早期方解石的胶结有利于后期次生孔隙的发育。不同凹陷次生孔隙发育的深度不同。在济阳坳陷西部的惠民凹陷次生孔隙主要发育于1500-2400m深度，向东至东营凹陷则主要发育于1650-2450m，再向东到沾化凹陷为2300-3500m，车镇凹陷为2200-2700m。从西向东、由南向北次生孔隙的发育深度逐步增大是受盆地沉积沉降中心的迁移规律控制的。  相似文献   

12.
Petrographic and SEM observations on 478 samples of six quartzose sandstones provide a data base that can be used to evaluate the role of intergranular pressure solution (IPS) in sandstone diagenesis and to constrain predictive models of the pressure solution process. SEM examination of grain contacts that have experienced pressure solution suggests that IPS occurs at the interior portions of contacts where the greatest stress is concentrated and that granulation of quartz grains at points of contact may contribute to the process. The chemical compaction fabrics that result from IPS suggest that the process is most commonly induced by effective lithostatic stress and that the resulting strain is uniaxial.Numerous geological variables influence IPS. Grain size exerts a fundamental influence, with finer grained samples experiencing more IPS than coarser grained samples. On both local and regional scales, IPS is inhibited by poor sorting, an abundance of ductile grains, the presence of “shallow” cement, slow rates of shallow burial, and overpressured conditions. In contrast, IPS is enhanced by the presence of illite grain coatings, increased maximum burial depth, rapid rates of shallow burial, longer times spent at great depths, higher temperatures, and high volumes and rates of fluid flow.Silica budgets indicate that some of the analyzed sandstones approximate mass balance whereas others have exported silica. Calculations of fluid flow requirements indicate that advanced stages of IPS are favored by high volume, high velocity fluid flow. Such flow can occur as a result of uplift of basin margins, which is typical of foreland and intractonic basins.  相似文献   

13.
Pore water chemistry and 234U/238U activity ratios from fine-grained sediment cored by the Ocean Drilling Project at Site 984 in the North Atlantic were used as constraints in modeling in situ rates of plagioclase dissolution with the multicomponent reactive transport code Crunch. The reactive transport model includes a solid-solution formulation to enable the use of the 234U/238U activity ratios in the solid and fluid as a tracer of mineral dissolution. The isotopic profiles are combined with profiles of the major element chemistry (especially alkalinity and calcium) to determine whether the apparent discrepancy between laboratory and field dissolution rates still exists when a mechanistic reactive transport model is used to interpret rates in a natural system. A suite of reactions, including sulfate reduction and methane production, anaerobic methane oxidation, CaCO3 precipitation, dissolution of plagioclase, and precipitation of secondary clay minerals, along with diffusive transport and fluid and solid burial, control the pore fluid chemistry in Site 984 sediments. The surface area of plagioclase in intimate contact with the pore fluid is estimated to be 6.9 m2/g based on both grain geometry and on the depletion of 234U/238U in the sediment via α-recoil loss. Various rate laws for plagioclase dissolution are considered in the modeling, including those based on (1) a linear transition state theory (TST) model, (2) a nonlinear dependence on the undersaturation of the pore water with respect to plagioclase, and (3) the effect of inhibition by dissolved aluminum. The major element and isotopic methods predict similar dissolution rate constants if additional lowering of the pore water 234U/238U activity ratio is attributed to isotopic exchange via recrystallization of marine calcite, which makes up about 10-20% of the Site 984 sediment. The calculated dissolution rate for plagioclase corresponds to a rate constant that is about 102 to 105 times smaller than the laboratory-measured value, with the value depending primarily on the deviation from equilibrium. The reactive transport simulations demonstrate that the degree of undersaturation of the pore fluid with respect to plagioclase depends strongly on the rate of authigenic clay precipitation and the solubility of the clay minerals. The observed discrepancy is greatest for the linear TST model (105), less substantial with the Al-inhibition formulation (103), and decreases further if the clay minerals precipitate more slowly or as highly soluble precursor minerals (102). However, even several orders of magnitude variation in either the clay solubility or clay precipitation rates cannot completely account for the entire discrepancy while still matching pore water aluminum and silica data, indicating that the mineral dissolution rate conundrum must be attributed in large part to the gradual loss of reactive sites on silicate surfaces with time. The results imply that methods of mineral surface characterization that provide direct measurements of the bulk surface reactivity are necessary to accurately predict natural dissolution rates.  相似文献   

14.
At burial depths of 800-1000 m, within the epicontinental Queensland Trough of north-east Australia (ODP Site 823), microcrystalline inter- and intraskeletal mosaics of anhedral (loaf-shaped, rounded) calcite have Sr2+ values ranging from below microprobe detection limits (<150 ppm) to 8100 ppm. Host rocks are well lithified, fine-grained mixed sediment to clayey wackestone and packstone of Middle and Late Miocene age. Petrography demonstrates that calcite precipitation has spanned shallow to deep burial, overlapping formation of framboidal pyrite in the upper 50 m; shallow-burial dolomitization (<300 m); and dedolomitization during sediment consolidation and incipient chemical compaction at greater (>400–500 m) depths. Petrographic observations illustrate that the calcite microfabric formed through coalescing crystal growth resulting from one or a combination of displacive growth in clay, porphyroid neomorphism of aragonite/vaterite, and clay replacement by calcite. Sr2+ mean concentrations in calcite between depths of 800 and 1000 m are similar to an expected equilibrium pore-water concentration, using a Dsr of 0.06, and may indicate active calcite precipitation. However, Sr2+ variation (2000–5000 ppm) within and among crystals, and concentrations that range well above predicted equilibrium values for a given depth, illustrate either variable Sr2+ retention during recrystallization of shelf-derived aragonite (and authigenic local vaterite) or relative uptake of Sr2+ during calcite precipitation with burial. Within the context of calcite formation during burial to 1 km, diagenetic attributes that affect the latter process include increased concentrations of pore-water Sr2+ with depth associated with aragonite recrystallization/dissolution; upward migration of Sr-rich pore water; and increased DSr related to local variation in precipitation/recrystallization rates, differential crystal sector growth rates and/or microvariation in aragonite distribution.  相似文献   

15.
Recovery of highly viscous oil from some of the deeper oil sand deposits of northern Alberta, Canada, is made possible through injection of heat by steam or hot water flooding of the reservoirs. The rise in temperature lowers the viscosity of the bitumen allowing it to be produced. The increase in temperature accelerates the reactions between the matrix and pore minerals of the formation and can produce reaction products which can significantly alter the permeability of the reservoir. If carbonate minerals are present in the reservoir, inorganic CO2 may also be a reaction product.

The Grand Rapids reservoir consists of relatively clean quartz sand containing 7 wt.% kaolinite, 1 wt.% calcite and a trace of smectite. Core floods of this sand by a neutral NaCl brine at 265°C, 8.2-MPa overburden pressure, 6.0-MPa fluid pressure and a flow velocity of 0.4 pore volumes per hour were used to determine the potential for hydrothermal reactions between clays and carbonate minerals in a natural reservoir sand. Reaction progress was followed by continuous sampling of the production fluids. The produced water was analyzed and the phase chemistry was calculated back to the run conditions using the computer code SOLMNEQF.

Mass-balance considerations on produced total inorganic carbon (TIC) show that calcite broke down very quickly, the maximum in CO2 production occurring after only one pore volume of fluid had passed through the core. The Ca released from the breakdown of calcite was incorporated in the formation of smectite as was shown by post-run clay mineral analysis by the following unbalanced chemical reaction:

calcite+kaolinite+H4Si04Ca-smectite+H20+CO2

Silica was supplied by the dissolution of quartz. Silica concentrations analyzed in the production fluid were depressed from those predicted by previously published quartz rate equations because of the rapid rate of smectite synthesis.

These observations were used to formulate the following model for the passage of the first pore volume of NaCl brine through the core. Initially calcite is present throughout the core. As the brine enters the inlet of the core, it equilibrates with calcite. The brine remains in equilibrium with calcite throughout the core as quartz and kaolinite react to form smectite. This model was tested with the computer code PATH.UBC using CO2 production as a measure of the progress variable ξ. A best fit was achieved to the produced fluid chemistry by varying relative dissolution rates of kaolinite and quatz and varying the suppression of precipitation of certain minerals.  相似文献   


16.
Hyperfiltration is sometimes cited as a mechanism to explain high degrees of calcite cementation at shale/sandstone contacts. To test this cementation mechanism, a series of experiments were performed in which solutions undersaturated with respect to calcite were hydraulically forced through a Ca-bentonite at different flow rates. Calcite precipitate was observed on the bentonite membrane from hyperfiltrated stock solutions having initial calcite saturation indices of 0.91 and 0.59. Supersaturation conditions at the clay's high-pressure interface are likely provided by establishment of a concentration polarization layer.In the subsurface, the driving force for hyperfiltration is a differential hydraulic pressure gradient acting across a shale membrane. This hydraulically-induced flux of solution causes a build-up of solute at the shale's high-pressure interface to levels that may exceed saturation indices of common cementing minerals like calcite. Although the source of the hydraulic pressure is likely due to compaction within the sedimentary pile, directional flow constraints suggest that hyperfiltration-induced precipitation of calcite occurs at sand/shale boundaries away from areas of active compaction.  相似文献   

17.
Pedogenic calcretes commonly exhibit clotted micrite, circum-granular calcite (grain coats) and microspar/spar veins. The three calcite-types with different dimensions were analyzed for their magnesium content to determine the relationship between crystal elongation and magnesium incorporation. The results show a very low MgO content for grain coats and microspars and high values for clotted micrite indicating that the ideal kinetic model does not hold true and several variables govern the end composition of calcites. The magnesium concentrations of meteoric calcites are genetically linked to the evolutionary history of the soil and climate. Grain coats, which are elongated calcites, contain the least amount of Mg and is related to the initial stages of pedogenesis wherein the limiting factor is the Mg/Ca ratio of the parent fluid. Lower magnesium contents arise due to smaller quantities of Mg being released during incipient weathering. Micrite morphology and composition is controlled by the greater availability of Mg ions through weathering, higher pCO2 in soil due to increased time-dependent soil respiration, which causes a rise in calcite precipitation rates and clay authigenesis. This in turn exerts a physical control on morphology by occluding pore space and providing numerous nuclei for calcite precipitation. The wide variability in spar cements is inherently controlled by inhomogeneties in parent fluid compositions with lower-than-micrite values on account of slower precipitation rates.  相似文献   

18.
Pedogenic calcretes commonly exhibit clotted micrite, circum-granular calcite (grain coats) and microspar/spar veins. The three calcite-types with different dimensions were analyzed for their magnesium content to determine the relationship between crystal elongation and magnesium incorporation. The results show a very low MgO content for grain coats and microspars and high values for clotted micrite indicating that the ideal kinetic model does not hold true and several variables govern the end composition of calcites. The magnesium concentrations of meteoric calcites are genetically linked to the evolutionary history of the soil and climate. Grain coats, which are elongated calcites, contain the least amount of Mg and is related to the initial stages of pedogenesis wherein the limiting factor is the Mg/Ca ratio of the parent fluid. Lower magnesium contents arise due to smaller quantities of Mg being released during incipient weathering. Micrite morphology and composition is controlled by the greater availability of Mg ions through weathering, higher pCO2 in soil due to increased time-dependent soil respiration, which causes a rise in calcite precipitation rates and clay authigenesis. This in turn exerts a physical control on morphology by occluding pore space and providing numerous nuclei for calcite precipitation. The wide variability in spar cements is inherently controlled by inhomogeneties in parent fluid compositions with lower-than-micrite values on account of slower precipitation rates.  相似文献   

19.
Carbonate mylonites with varying proportions of second-phase minerals were collected at positions of increasing metamorphic grade along the basal thrust of the Morcles nappe (Helvetic nappes, Switzerland). Variations of temperature, stress, and strain rate, changes in chemistry of solid and fluid phases, and differing degrees of strain localization and annealing were tracked by measuring the shapes, mean sizes, and size distributions of both matrix and second-phase grains, as well as crystal preferred orientation (CPO) of the matrix. Field structures suggest that strain rate was constant along the fault. The mean and distribution of the calcite grain sizes were affected most profoundly by temperature: Increased temperature, presumably accompanied by decreased stress, correlated with larger mean sizes and wider size distributions. At a given location, the matrix grains in mylonites with more second-phase particles are, on average, smaller, have narrower size distributions, and have more elongate shapes. For example, mylonites with 50 vol.% of second phases have matrix grain sizes half that of pure mylonites. Changes in calcite chemistry and the presence of synkinematic fluids seemed to influence microfabric only weakly. Temporal variations in conditions, such as exhumation-induced cooling, apparently provoke changes in temperature, stress, and strain rate along the nappe. These changes result in further strain localization during retrograde conditions and cause the grain size to be reduced by an additional 50%. The matrix CPO strengthens with increasing temperature or strain, but weakens and rotates with increasing second-phase content. These fabric changes suggest differing rates of grain growth, grain size reduction, and development of CPO owing to variations in the deformation conditions and, perhaps, mechanisms. To interpret natural mylonite structures or to extrapolate mechanical data to natural situations requires careful characterization of the microfabric, and, in particular, second-phase minerals.  相似文献   

20.
The Middle Jurassic Khatatba Formation acts as a hydrocarbon reservoir in the subsurface in the Western Desert, Egypt. This study, which is based on core samples from two exploration boreholes, describes the lithological and diagenetic characteristics of the Khatatba Formation sandstones. The sandstones are fine‐ to coarse‐grained, moderately to well‐sorted quartz arenites, deposited in fluvial channels and in a shallow‐marine setting. Diagenetic components include mechanical and chemical compaction, cementation (calcite, clay minerals, quartz overgrowths, and a minor amount of pyrite), and dissolution of calcite cements and feldspar grains. The widespread occurrence of an early calcite cement suggests that the Khatatba sandstones lost a significant amount of primary porosity at an early stage of its diagenetic history. In addition to calcite, several different cements including kaolinite and syntaxial quartz overgrowth occur as pore‐filling and pore‐lining cements. Kaolinite (largely vermicular) fills pore spaces and causes reduction in the permeability of the reservoir. Based on framework grain–cement relationships, precipitation of the early calcite cement was either accompanied by or followed the development of part of the pore‐lining and pore‐filling cements. Secondary porosity development occurred due to partial to complete dissolution of early calcite cements and feldspar. Late kaolinite clay cement occurs due to dissolved feldspar and has an impact on the reservoir quality of the Khatatba sandstones. Open hydraulic fractures also generated significant secondary porosity in sandstone reservoirs, where both fractures and dissolution took place in multiple phases during late diagenetic stages. The diagenesis and sedimentary facies help control the reservoir quality of the Khatatba sandstones. Fluvial channel sandstones have the highest porosities and permeabilities, in part because of calcite cementation, which inhibited authigenic clays or was later dissolved, creating intergranular secondary porosity. Fluvial crevasse‐splay and marine sandstones have the lowest reservoir quality because of an abundance of depositional kaolinite matrix and pervasive, shallow‐burial calcite and quartz overgrowth cements, respectively. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   

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