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1.
Dolomite [Ca,Mg(CO3)2] precipitation from supersaturated ionic solutions at Earth surface temperatures is considered kinetically inhibited because of the difficulties experienced in experimentally reproducing such a process. Nevertheless, recent dolomite is observed to form in hypersaline and alkaline environments. Such recent dolomite precipitation is commonly attributed to microbial mediation because dolomite has been demonstrated to form in vitro in microbial cultures. The mechanism of microbially mediated dolomite precipitation is, however, poorly understood and it remains unclear what role microbial mediation plays in natural environments. In the study presented here, simple geochemical methods were used to assess the limitations and controls of dolomite formation in Deep Springs Lake, a highly alkaline playa lake in eastern California showing ongoing dolomite authigenesis. The sediments of Deep Springs Lake consist of unlithified, clay‐fraction dolomite ooze. Based on δ18O equilibria and textural observations, dolomite precipitates from oxygenated and agitated surface brine. The Na‐SO4‐dominated brine contains up to 500 mm dissolved inorganic carbon whereas Mg2+ and Ca2+ concentrations are ca 1 and 0·3 mm , respectively. Precipitation in the subsurface probably is not significant because of the lack of Ca2+ (below 0·01 mm ). Under such highly alkaline conditions, the effect of microbial metabolism on supersaturation by pH and alkalinity increase is negligible. A putative microbial effect could, however, support dolomite nucleation or support crystal growth by overcoming a kinetic barrier. An essential limitation on crystal growth rates imposed by the low Ca2+ and Mg2+ concentrations could favour the thermodynamically more stable carbonate phase (which is dolomite) to precipitate. This mode of unlithified dolomite ooze formation showing δ13C values near to equilibrium with atmospheric CO2 (ca 3‰) contrasts the formation of isotopically light (organically derived), hard‐lithified dolomite layers in the subsurface of some less alkaline environments. Inferred physicochemical controls on dolomite formation under highly alkaline conditions observed in Deep Springs Lake may shed light on conditions that favoured extensive dolomite formation in alkaline Precambrian oceans, as opposed to modern oceans where dolomites only form diagenetically in organic C‐rich sediments.  相似文献   

2.
Atomistic computer simulation methods have been used to model the nature of nonstoichiometry and impurity defects in the bulk and at the (101?4) surface of dolomite (MgCa(CO3)2). Calcium and Mg in the bulk and at the surface have been replaced with divalent Ni, Co, Zn, Fe, Mn, and Cd. The results of these calculations indicate that in the bulk, these impurities will prefer to substitute at the Ca site rather than the Mg site. Ca excess in dolomite is most likely incorporated as basal stacking faults; this nonstoichiometry can influence the site distribution of impurities. The calculated surface segregation energies suggest that of all the impurities studied, only Cd will show a strong preference for the (101?4) surface of dolomite.  相似文献   

3.
The Late Cretaceous to Early Eocene, dominantly micritic, Amuri Limestone Group (ALG) was deposited in an approximately NW trending trough, in eastern Marlborough, New Zealand. The ALG comprises: the Mead Hill Formation; the Teredo, Lower and Middle Limestone formations; and the Upper and Lower Marl formations. Chert and dolomite are concentrated in the Mead Hill Formation, which contains five of six recognized diagenetic zones: Zone I at the base of the ALG consists almost entirely of chert; Zone II consists solely of chert and dolomite; Zone III comprises chert and limestone; Zone IV is composed of chert plus dolomite; Zone V is a chertified mudstone; and the minor amounts of chert found in the Middle Limestone Formation comprise Zone VI. With the exception of Zones IV and V, chert decreases stratigraphically upwards and away from the basin centre. All the dolomites are composed of <1 mm diameter rhombohedra in discontinuous beds and lenses. Generally Ca-rich, and non- to slightly ferroan, the dolomite contains approximately 500–900 ppm Mn and 200–400 ppm Sr. δ13C values average 1–2%PDB with δ18O ratios of about -4%PDB. Mass balance calculations indicate that the Mg2+ for dolomitization was derived from sea water. Sr, Fe and Mn concentrations are interpreted as indicating dolomite formation in the marine environment, with no influence from meteoric waters. The intimate association with pyrite implies dolomite formation in association with sulphate reduction, in the upper sediment column. δ18O data show that the bulk of the dolomite formed at temperatures below 50°C. All chert samples contain in excess of 90 wt% SiO2, about 1 wt% Al2O3 and 1 wt% from losses on ignition. Generally all other major elements total less than 2 wt% oxide. δ18O values range from 26·8 to 29·0%SMOW. Chert chemistry is consistent with the replacement of host carbonate and expulsion of carbonate-bound components from the site of chertification, and the effective dilution by SiO2 of non-carbonate-bound insoluble residues. δ18O data indicate that chert formed in fluids of similar composition and temperature as the dolomite. The abundance of disseminated pyrite in cherts implies an association with sulphate reduction. Silica for chertification is thought to have initially come from dissolution of siliceous organisms. However, there is insufficient biogenic silica available to form the volumes of chert observed. It is suggested that the bulk of the silica came from SiO2-rich pore waters generated by clay mineral reactions in the thick underlying mudstones. The ALG compacted down through these pore waters. Chert and dolomite nucleation are considered to have been penecontemporaneous. Dolomitization was initially probably the faster process, continuing as long as sulphate reduction prevailed and there was an adequate supply of Mg2+. The nucleation of chert, although initially slower (probably due to a relatively lower initial SiO2 supply), continued after cessation of dolomitization to the extent of completely chertifying the dolomite intercrystalline matrix. The amount of chertification decreased progressively as SiO2 supplies diminished, both stratigraphically upwards and away from the basin centre.  相似文献   

4.
The structure and reactivity of the dolomite (104)-water interface was probed in situ with high resolution X-ray reflectivity and surface force microscopy at room temperature. Measurements in stoichiometric solutions alternating between saturated and supersaturated (log IAP/K = 2.3) conditions show that the dolomite surface termination readily changes in response to solution composition, but these changes are self-limiting and partially irreversible. The freshly cleaved dolomite (104) surface in contact with the saturated solution has a stoichiometric termination, a distinct surface hydration layer and small surface structural displacements, similar to those observed previously at the calcite-water interface. After reaction with supersaturated solutions dolomite is terminated by a two-layer thick Ca-rich film with substantial structural displacements of the cations. With subsequent exposure to a saturated solution this surface was transformed to an interfacial structure different from the freshly cleaved surface, having a reduced density of the outermost surface layer and a Ca-rich second layer. These results provide new insight into the lack of dolomite growth in modern carbonate environments (i.e., the “dolomite problem”), suggesting that this behavior is associated with a combination of thermodynamic and kinetic factors, including (1) growth of compositionally modified epitaxial CaXMg2−X(CO3)2 layers having thicknesses limited by lattice strain, (2) slow incorporation of Mg during layer growth, and (3) partial irreversibility of surface reactions.  相似文献   

5.
《Geochimica et cosmochimica acta》1999,63(19-20):3133-3143
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6.
Spheroidal dolomite cements are a pervasive and distinctive feature in five exposed lithologies of different geological age in Kuwait. The spheroids range in diameter from ～5–350 μm, have concentric zones and nuclei of fluid inclusions with or without a radial fabric, and compositions varying from near stoichiometric to Ca56 Mg44. All spheroids appear to be primary in origin with no evidence of replacement. Some concentric zones show selective calcitization and/or leaching. Most of these features are confined to within 30 m of the surface. Consequently, spheroidal dolomites recognizable at depth in ancient sequences may be indicative of a local unconformity. The dolomite distributions are areally correlative with known areas of hydrocarbon seepage, the latter being confined to prominent oil field anticlinal trends. It is proposed that the dolomitization was caused by groundwaters carrying hydrocarbons to the surface, which were then oxidized to carbon dioxide. The gas bubbles may have acted as nuclei for spheroid growth with a possible inducement by bacteria which have an affinity for hydrocarbons. The implication is that the regional distribution of spheroidal dolomites may be an indicator of a potential reservoir facies at depth.  相似文献   

7.
The potential for metal release associated with CO2 leakage from underground storage formations into shallow aquifers is an important consideration in assessment of risk associated with CO2 sequestration. Metal release can be driven by acidification of groundwaters caused by dissolution of CO2 and subsequent dissociation of carbonic acid. Thus, acidity is considered one of the main drivers for water quality degradation when evaluating potential impacts of CO2 leakage. Dissolution of carbonate minerals buffers the increased acidity. Thus, it is generally thought that carbonate aquifers will be less impacted by CO2 leakage than non-carbonate aquifers due to their high buffering potential. However, dissolution of carbonate minerals can also release trace metals, often present as impurities in the carbonate crystal structure, into solution. The impact of the release of trace metals through this mechanism on water quality remains relatively unknown. In a previous study we demonstrated that calcite dissolution contributed more metal release into solution than sulfide dissolution or desorption when limestone samples were dissolved in elevated CO2 conditions. The study presented in this paper expanded our work to dolomite formations and details a thorough investigation on the role of mineral composition and mechanisms on trace element release in the presence of CO2. Detailed characterization of samples from dolomite formations demonstrated stronger associations of metal releases with dissolution of carbonate mineral phases relative to sulfide minerals or surface sorption sites. Aqueous concentrations of Sr2+, CO2+, Mn2+, Ni2+, Tl+, and Zn2+ increased when these dolomite rocks were exposed to elevated concentrations of CO2. The aqueous concentrations of these metals correlate to aqueous concentrations of Ca2+ throughout the experiments. All of the experimental evidence points to carbonate minerals as the dominant source of metals from these dolomite rocks to solution under experimental CO2 leakage conditions. Aqueous concentrations of Ca2+ and Mg2+ predicted from numerical simulation of kinetic dolomite dissolution match those observed in the experiments when the surface area is three to five orders of magnitude lower than the surface area of the samples measured by gas adsorption.  相似文献   

8.
Examination with scanning electron microscopy (SEM) and scanning force microscopy (SFM) revealed etch pits, layers and islands on dolomite crystal faces synthesized from calcite in Ca‐Mg‐Cl solutions at 200 °C and a wide variety of natural dolomites. Layers are broad, flat structures bounded by steps less than 100 nm high and greater than 1 μm wide. Islands are rounded topographic highs <20 nm high and <200 nm wide. The nanotopography of synthetic dolomite changed from islands throughout most of the reaction to layers at 100% dolomite. Island nanotopography formed on both Ca‐rich and near‐stoichiometric dolomite. Analyses of reaction products from dolomite synthesis indicates that there are no SFM‐detectable products formed in <10 h. SEM‐detectable products formed in 15 h. X‐ray diffraction (XRD)‐detectable products formed in ≈18 h, and the reaction went to completion in ≈40 h. Based on SFM analyses, the induction period for dolomitization in these experiments accounts for ≈20% of the total reaction time necessary to dolomitize CaCO3 completely under the experimental conditions used here. Island nano‐ topography is inferred to occur at higher degrees of supersaturation than layer nanotopography for three reasons. First, island nanotopography on synthetic calcite and gypsum forms at higher supersaturations than layer nanotopography. Secondly, island nanotopography formed in solutions with higher degrees of supersaturation with respect to dolomite. Thirdly, the greater surface roughness of a crystal face composed of islands compared with layers indicates that island surfaces have higher surface energy than layer surfaces. Therefore, the stability of island surfaces requires a higher degree of supersaturation. Because islands and layers form under a wide range of conditions, their presence provides broadly applicable criteria for evaluating relative degrees of supersaturation under which ancient dolomite formed. Comparison of synthetic dolomites with natural dolomites demonstrates (1) similar nanotopography on natural and synthetic dolomites and (2) both natural planar and non‐planar dolomite may have island nanotopography.  相似文献   

9.
Cleaved surfaces of dolomite were studied using ex-situ X-ray photoelectron spectroscopy (XPS) following exposure of the surfaces to various experimental conditions. Dolomite samples exposed to air, to a highly undersaturated solution (0.1 M NaCl, pH = 9), and to solution with a supersaturation (−Δμ/kT) of 5.5 (pH = 9) were investigated with semiquantitative methods of analysis to ascertain the degree of non-stoichiometry resulting at the dolomite surface from reactive conditions. It was found that the dolomite cleavage surface in undersaturated solution was not altered significantly from the stoichiometric surface termination. The composition of the cleaved surface after exposure to supersaturated solution, a surface known to have self-limiting growth characteristics under similar conditions, was found to be Ca2+ rich (CaxMg2 − x(CO3)2, 1.7 > x > 1.3). The observations, while underscoring differences in hydration/dehydration kinetics of the two alkaline earth cations, suggest that achievement of equilibrium at dolomite-water interfaces may be subject to significant barriers from both undersaturated and supersaturated solutions.  相似文献   

10.
塔里木盆地寒武系盐下白云岩作为重要的战略接替区已成为近年来的研究热点。前人主要集中对寒武系白云岩的形成机制和膏盐岩的封盖作用进行了研究,而关于膏盐岩对白云岩储层的影响则少有涉及。本文总结了塔里木盆地寒武系白云岩储层特征,同时探讨了膏盐岩对白云岩储层的影响机制,以期为寒武系盐下白云岩勘探提供指导。塔里木盆地寒武系白云岩主要分为结晶白云岩和微生物白云岩两大类,其中结晶白云岩又可分为泥微晶白云岩、晶粒白云岩和颗粒白云岩,微生物白云岩又可分为凝块石白云岩、叠层石白云岩和泡沫绵石白云岩。受膏盐岩影响的白云岩储层类型可划分为膏溶孔型白云岩储层、晶间孔型白云岩储层和溶蚀孔型白云岩储层。蒸发潮坪环境中,膏盐岩的沉淀有利于克服白云石化的Mg2+的动力学障碍而形成白云岩,同时,微生物作用下SO24-的还原会促进白云石的沉淀。膏盐岩对白云岩储层孔隙的影响主要体现在:含硬石膏结核泥粉晶白云岩易于形成膏溶孔型白云岩储层;膏盐层较高的热导率有利于倒退溶蚀作用的发生;近地表低温条件下硫酸盐的溶解有利于白云石的沉淀;热化学硫酸盐还原作用形成酸性气体有利于深埋溶蚀作用,形成溶蚀孔型白云岩储层。  相似文献   

11.
In past decades, the formation of dolomite at low temperature has been widely studied in both natural systems and cultured experiments, yet the mechanism(s) involved in the nucleation and precipitation of dolomite remains unresolved. Late Eocene dolomitic deposits from core in the upper Niubao Formation (Lunpola Basin, central Tibetan Plateau, China) are selected as a case study to understand the dolomitization process(es) in the geological record. Dolomite formation in Lunpola Basin can be ascribed to a different mechanism forming the large quantities of replacive dolostones in the geological record; and provides a potential fossil analogue for primary dolomite precipitation at low temperature. This analogue consists of an alternation of laminated dolomitic beds, organic-rich and siliciclastic layers; formed in response to intense evaporation interpreted to take place in a continental shallow lake environment. Mineralogical, textural and stable isotopic evaluations suggest that the dolomite from those dense-clotted laminated beds is a primary precipitate. At the nanoscale, these dolomitic beds are composed of Ca–Mg carbonate globular nanocrystals (diameter 80 to 100 nm) embedded in an organic matrix and attached to clay flakes. Micro-infrared spectroscopy analyses have revealed the presence of aliphatic compounds in the organic matrix. Microscopic and elemental compositional studies suggest that clay surfaces may facilitate the nucleation of dolomite at low temperature in the same way as the organic matrix does. The dolomite laminae show values for δ18OVPDB from −3.2 to −1.76‰ and for δ13CVPDB from −2.62 to −3.78‰. Inferred δ18OSMOW values of the lake water reveal typical evaporitic hydrological conditions. These findings provide a potential link to primary dolomite formation in ancient and modern sedimentary environments; and shed new light on the palaeoenvironmental conditions in central Tibet during the Eocene.  相似文献   

12.
ALI M'RABET 《Sedimentology》1981,28(3):331-352
Combined field, sedimentological, mineralogical, isotopic and geochemical study of the Lower Cretaceous dolomites of Central Tunisia has demonstrated considerable diversity in origin. Environments of dolomite formation include deep phreatic, karst, lacustrine and evaporitic sabkha. All four groups of dolomite are composed of non-stoichiometric and/or disordered crystals which are more or less rich in calcium and in iron. Petrographic fabrics are of three types: replacement, recrystallization and cementation. These three fabrics are proposed among the various criteria for the different environments of dolomitization. Average isotope (δ18 O and δ13 C) contents for these four dolomite groups range from ?10·5 to +0·4%o (PDB) and ?3·9 to + 3·7%o respectively. The distribution of strontium is related both to the degree of recrystallization and to the palaeosalinity. Ferrous iron, also very common, is regarded as an indicator of relatively deep reducing conditions, mainly in meteoric groundwaters. Sodium distribution is related to inclusions within the dolomite, its distribution being relatively constant in all four groups; it cannot be regarded as a reliable criterion for palaeosalinity of dolomitizing fluids. This study confirms that dolomitization may occur under widely different palaeoenvironments, either at the surface or during burial. With the exception of the sabkha environment, dolomitizing fluids seem to have been essentially meteoric.  相似文献   

13.
Microstructure‐based finite-element analysis with a microcracking algorithm was used to simulate an actual degradation phenomenon of marble structures, i.e., microcracking. Both microcrack initiation and crack propagation were characterized, as were their dependence on lattice preferred orientation (LPO), grain shape preferred orientation (SPO), grain size, marble composition (calcite and dolomite) and grain‐boundary fracture toughness. Two LPOs were analyzed: a random orientation distribution function and an orientation distribution function with strong directional crystalline texture generated from a March–Dollase distribution. Three SPOs were considered: equiaxed grains; elongated grains and a mixture of equiaxed and elongated grains. Three different grain sizes were considered: fine grains of order 200 μm (only calcitic marble); medium size grains of order 1 mm (calcitic and dolomitic marbles); and large grains of order 2 mm (only dolomitic marble). The fracture surface energy for the grain boundaries, γig, was chosen to be 20 and 40 % of the fracture surface energy of a grain, γxtal, so that both intergranular and transgranular fracture were possible. Studies were performed on these idealized marble microstructures to elucidate the range of microcracking responses. Simulations were performed for both heating and cooling by 50 °C in steps of 1 °C. Microcracking results were correlated with the thermoelastic responses, which are indicators related to degradation. The results indicate that certain combinations of LPO, SPO, grain size, grain‐boundary fracture toughness and marble composition have a significant influence on the thermal-elastic response of marble. Microstructure with the smallest grain size and the highest degree of SPO and LPO had less of a tendency to microcrack. Additionally, with increasing SPO and LPO microcracking becomes more spatially anisotropic. A significant observation for all microstructures was an asymmetry in microcracking upon heating and cooling: more microcracking was observed upon cooling than upon heating. Given an identical microstructure and crystallographic texture, calcite showed larger thermal stresses than dolomite, had an earlier onset of microcracking upon heating and cooling, and a greater microcracked area at a given temperature differential. Thermal expansion coefficients with and without microcracking were also determined.  相似文献   

14.
Door County, Wisconsin, is a region of karst topography underlain by Silurian dolomite bedrock. Numerous sinkholes intercept much of the surface runoff and act as sites for direct groundwater recharge. The clay-rich and impermeable Upper Ordovician Maquoketa formation separates the dolomite aquifer from the deeper aquifers and appears to be a factor in groundwater circulation and karst formation Thin glacial drift and Quaternary materials overlie the dolomite and are hydrologically connected with it The interactions of surface and groundwater, and the role of solution features in water interchange were studied in a small drainage basin. This basin contains several large sinkholes and a nearby spring complex Mapping identified many additional sinks and swallets in surface drainage routes Water flowing into two sinks was traced and found to have a residence time of several hours. Water flowing into sinkholes and from the spring was sampled to identify the quality and seasonal trends in composition of the shallow groundwater Water quality parameters monitored include magnesium, sodium, potassium, chloride, phosphorous, nitrate and ammonia, nitrogen, alkalinity, pH, turbidity, and specific conductance. Nitrate levels were found to increase 5 to 6 times during periods when there was zero input through sinkhole recharge sites. Nitrate levels approached the 10 mg/l NO3 −-N limit set by the U.S. Public Health Service for drinking water In this basin sandy soils are most susceptible to sink development, whereas clay-rich soils have a lesser number of sinks. It appears, however, that a network of bedrock solution features exists under all soils The loss of soil into sinkholes has impacted groundwater quality and reduced agricultural productivity through a reduction in tillable acreage and water retention capacity.  相似文献   

15.
ABSTRACT Gravity cores of Holocene sediments from a shallow ephemeral lake in the Coorong region (Pellet Lake, southeastern coastal Australia) show a mineral assemblage and sequence particular to its hydrology. The mineralogical sequence above an initial dolomitic siliciclastic sand reflects conditions of increasing salinity in the lower portions of the core (i.e. organic-rich aragonite to magnesite + hydromagnesite + aragonite) followed by a relative decrease in salinity (i.e. magnesite + aragonite + hydromagnesite to aragonite + hydromagnesite) in the upper portions of the core. This sequence is capped by ? 0.4 m of micritic dolomite and minor amounts of hydromagnesite, with the relative abundance of dolomite increasing upwards. Three stratigraphically and spatially distinct dolomite units (upper, lower and margin) are recognized using stable carbon and oxygen isotope data, unit cell calculations and MgCO3 mole per cent data of the dolomite. Detailed X-ray diffraction (XRD) analyses of samples with more than 80% dolomite shows that the dolomite is ordered. Average unit cell parameters, calculated from the XRD patterns, indicate that the upper dolomite unit has crystal lattices expanded in the co direction (co= 16.09 Å) relative to ideal dolomite (co= 16.02 Å) and contracted in the ao direction (ao= 4.796 Å) relative to ideal dolomite (ao= 4.812 Å). The mol fraction of MgCO3 in the upper dolomite shows up to 4.0 ±M 2.0 mole per cent excess Mg in the dolomite crystal lattice (calculated from XRD). This unusual dolomite crystal chemistry is probably generated by rapid precipitation from solutions which have greatly elevated Mg/Ca ratios. Transmission electron microscopy reveals that the upper dolomite has a heterogeneous microstructure which also suggests rapid precipitation from solution. The modulated microstructure found in calcium-rich dolomite is completely lacking. Dolomite ordering reflections are present in electron diffraction patterns, but are weak. Stable oxygen and carbon isotope values of the upper dolomite are tightly grouped (ave. δ18O ～+ 7.55%o, δ13C ～+ 4.10%o), yet show three upward-lightening oxygen cycles. The oxygen cycles correlate with three upward decreases in the calculated Mg content of the dolomite zone. These cycles may indicate the increased importance of rain-water dilution of the brine at times when the water in the lake was at its shallowest levels. Analyses of the lower dolomite and the margin dolomite suggest that these units precipitated more slowly from less evaporitic brines than the upper dolomite unit. The lower dolomite is close to stoichiometric, has less evaporitic stable isotope values than the upper dolomite, and has only a slightly expanded co-axis. The margin dolomite is Ca-rich, has a more homogeneous microstructure, and has expanded ao and co axes. The abundance of relatively soluble Mg-bearing phases, such as hydromagnesite and magnesite, may supply additional magnesium for the dolomitization of aragonite and calcite during subsequent diagenesis and burial of the sediment. This process may leave a finely laminated dolomicrite deposit which retains little, if any, evidence of evaporite minerals.  相似文献   

16.
The surface effect on the isotopic fractionation between CO2 and calcite, dolomite and witherite has been studied through gas-solid exchange experiments. Oxygen isotope fractionation between surface calcite and CO2 was found to be higher by 5–6%. than the fractionation between bulk calcite and CO2.Similar studies were made using dolomite and witherite. The dolomite-calcite and witheritecalcite fractionation evaluated through the surface exchange with CO2 were found to be close to values determined by other workers under controlled conditions in the laboratory.  相似文献   

17.
Stoichiometric mixtures of tremolite and dolomite were heated to 50° C above equilibrium temperatures to form forsterite and calcite. The pressure of the CO2-H2O fluid was 5 Kb and \(X_{{\text{CO}}_{\text{2}} }\) varied from 0.1 to 0.6. The extent of the conversion was determined by the amount of CO2 produced. The resulting mixtures of unreacted tremolite and dolomite and of newly-formed forsterite and calcite were examined with a scanning electron microscope. All tremolite and dolomite grains showed obvious signs of dissolution. At fluid compositions with \(X_{{\text{CO}}_{\text{2}} }\) less than about 0.4, the forsterite and calcite crystals are randomly distributed throughout the charges, indicating that surfaces of the reactants are not a controlling factor with respect to the sites of nucleation of the products. A change is observed when \(X_{{\text{CO}}_{\text{2}} }\) is greater than about 0.4; the forsterite and calcite crystals now nucleate and grow at the surface of the dolomite grains, thus indicating a change in mechanism at medium CO2 concentrations. As the reaction progresses, the dolomite grains become more and more surrounded by forsterite and calcite, finally forming armoured relics of dolomite. Under experimental conditions this characteristic texture can only be formed if the CO2-concentration is greater than about 40 mole %. These findings make it possible to estimate the CO2-concentration from the texture of the dolomite+tremolite+forsterite+calcite assemblage. The results suggest a dissolution-precipitation mechanism for the reaction investigated. In a simplified form it consists of the following 4 steps:
  1. Dissolution of the reactants tremolite and dolomite.
  2. Diffusion of the dissolved constituents in the fluid.
  3. Heterogeneous nucleation of the product minerals.
  4. Growth of forsterite and calcite from the fluid.
Two possible explanations are discussed for the development of the amoured texture at \(X_{{\text{CO}}_{\text{2}} }\) above 0.4. The first is based upon the assumption that dolomite has a lower rate of dissolution than tremolite at high \(X_{{\text{CO}}_{\text{2}} }\) values resulting in preferential calcite and forsterite nucleation and growth on the dolomite surface. An alternative explanation is the formation of a raised CO2 concentration around the dolomite grains at high \(X_{{\text{CO}}_{\text{2}} }\) values, leading to product precipitation on the dolomite crystals.  相似文献   

18.
Microbial mediation is the only demonstrated mechanism to precipitate dolomite under Earth surface conditions. A link between microbial activity and dolomite formation in the sabkha of Abu Dhabi has, until now, not been evaluated, even though this environment is cited frequently as the type analogue for many ancient evaporitic sequences. Such an evaluation is the purpose of this study, which is based on a geochemical and petrographic investigation of three sites located on the coastal sabkha of Abu Dhabi, along a transect from the intertidal to the supratidal zone. This investigation revealed a close association between microbial mats and dolomite, suggesting that microbes are involved in the mineralization process. Observations using scanning electron microscopy equipped with a cryotransfer system indicate that authigenic dolomite precipitates within the exopolymeric substances constituting the microbial mats. In current models, microbial dolomite precipitation is linked to an active microbial activity that sustains high pH and alkalinity and decreased sulphate concentrations in pore waters. Such models can be applied to the sabkha environment to explain dolomite formation within microbial mats present at the surface of the intertidal zone. By contrast, these models cannot be applied to the supratidal zone, where abundant dolomite is present within buried mats that no longer show signs of intensive microbial activity. As no abiotic mechanism is known to form dolomite at Earth surface conditions, two different hypotheses can reconcile this result. In a first scenario, all of the dolomite present in the supratidal zone formed in the past, when the mats were active at the surface. In a second scenario, dolomite formation continues within the buried and inactive mats. In order to explain dolomite formation in the absence of active microbial metabolisms, a revised microbial model is proposed in which the mineral‐template properties of exopolymeric substances play a crucial role.  相似文献   

19.
Summary New data on Sr and Nd isotope composition and major and trace element distribution in dolomite-calcite carbonatite dykes at Bayan Obo are provided, and a Mid-Proterozoic age is deduced. The dykes and the neighbouring massive dolomite (H8) body have similar geochemical characteristics, interpreted to indicate a carbonatitic magmatic origin. The occurrence of riebeckite-bearing fenitized quartzites marginal to both dykes and H8 dolomite body, and the presence of xenoliths in the latter, supports this conclusion. Taken together with previously published stable isotope data, these data confirm a mantle-derived origin for the H8 body. The oxygen isotope composition of the dolomite and magnetite in the dykes is lower than that in the fine-grained dolomite. Oxygen data from samples of the coarse-grained dolomite host are either similar to the dykes or to the fine-grained type in agreement with their other geochemical characteristics. The carbonate-magnetite thermometric pairs of the fine-grained dolomite indicate a range of 350–540 °C, which is probably lower than that of the original main magmatic emplacement. This supports the distinction made between the original coarse-grained dolomite marble and dyke composition from the later fine-grained dolomite. Thus the large H8 dolomite is interpreted as a carbonatite intrusion that contains wall-rock xenoliths and caused fenitization of the hanging wall, foot wall and the xenoliths, and that the coarse-grained portions of the H8 marble are those portions that, in the Late Proterozoic to Palaeozoic, escaped recrystallization to fine-grained dolomite and subsequent REE-Fe mineralization. Currently at National Oceanography Centre, University of Southampton, Southampton, UK An erratum to this article is available at .  相似文献   

20.
Dolomite [CaMg(CO3)2] is abundant in sedimentary rocks throughout the geological record, but it is rarely found in modern sediments. Also, it cannot be precipitated under low‐temperature conditions in the laboratory without microbial mediation and, as a result, its origin remains a long‐standing enigma. This study reports biologically mediated dolomite precipitation in ancient microbial mats and biofilms from the Cambrian Tarim Basin. The ambient temperature at the time of dolomite precipitation was estimated from δ18O values from early diagenetic dolomite, and the presence of structures associated with extracellular polymeric substances (EPS), is composed of fibres arranged in a reticular pattern, would favour epitaxial crystallization of dolomite on an organic substrate. In addition, poorly crystallized dolomite formed nanocrystal aggregates that strongly resemble the morphology and size distribution observed in microbial culture experiments. These lines of evidence confirm that microbial structures can be preserved in ancient dolomite and validate their use as biosignatures.  相似文献   

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