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1.
N. L. WATTS 《Sedimentology》1980,27(6):661-686
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2.
High concentrations of fluoride (up to 7.6 mg/L) are a recognized feature of the Wailapally granitic aquifer of Nalgonda District, Andhra Pradesh, India. The basement rocks provide abundant sources of F in the form of amphibole, biotite, fluorite and apatite. The whole-rock concentrations of F in the aquifer are in the range 240–990 mg/kg. Calcretes from the shallow weathered horizons also contain comparably high concentrations of F (635–950 mg/kg). The concentrations of water-soluble F in the granitic rocks and the calcretes are usually low (1% of the total or less) but broadly correlate with the concentrations observed in groundwaters in the local vicinity. The water-soluble fraction of fluoride is relatively high in weathered calcretes compared to fresh calcretes.Groundwater major-ion composition shows a well-defined trend with flow downgradient in the Wailapally aquifer, from Na–Ca–HCO3-dominated waters in the recharge area at the upper part of the catchment, through to Na–Mg–HCO3 and ultimately to Na–HCO3 and Na–HCO3–Cl types in the discharge area in the lowest part. The evolution occurs over a reach spanning some 17 km. Groundwater chemistry evolves by silicate weathering reactions, although groundwaters rapidly reach equilibrium with carbonate minerals, favouring precipitation of calcite, and ultimately dolomite in the lower parts of the watershed. This precipitation is also aided by evapotranspiration. Decreasing Ca activity downgradient leads to a dominance of fluorite-undersaturated conditions and consequently to mobilisation of F. Despite the clear downgradient evolution of major-ion chemistry, concentrations of F remain relatively uniform in the fluorite-undersaturated groundwaters, most being in the range 3.0–7.6 mg/L. The rather narrow range is attributed to a mechanism of co-precipitation with and/or adsorption to calcrete in the lower sections of the aquifer. The model may find application in other high-F groundwaters from granitic aquifers of semi-arid regions.  相似文献   

3.
文章以桂林典型岩溶区和非岩溶区土壤剖面为研究对象,采用改进的Tessier元素形态连续提取法,测定岩溶区和非岩溶区土壤钙（Ca）和镁（Mg）元素离子交换态（包括水溶态）、碳酸盐结合态、腐殖酸结合态、铁锰氧化物结合态、强有机质结合态（包括部分硫化物）和残渣态等形态,探讨岩溶区和非岩溶区土壤Ca、Mg形态在土壤剖面中的迁移变化特征。结果表明:（1）岩溶区石灰土剖面中,随剖面深度加深,pH值增大,而土壤有机质、全氮（N）、全磷（P）含量减少,Ca元素主要以交换态存在且在各土壤剖面中含量相近,Mg元素主要是以残渣态赋存在土壤剖面中,随着土壤剖面深度腐殖酸结合态百分比减少,存在累积现象;（2）在非岩溶地区酸性土壤中,土壤总钙较低。在土壤剖面0~60 cm以强有机结合态为主,深层剖面（大于60 cm）以残渣态为主;Mg元素有效态含量较低,非岩溶区土壤Mg元素以腐殖酸结合态和残渣态为主,与岩溶区土壤类似,非岩溶区Mg元素在土壤中也存在一定累积。   相似文献   

4.
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   

5.
The Lake Afourgagh sediment record and facies successions provide an outstanding example of environmentally controlled carbonate sedimentation. Afourgagh is a small, shallow permanent lake located in the Middle‐Atlas Mountains in Morocco in a karstic context. It is fed by ground waters that are relatively enriched in Mg resulting from the leaching of the Jurassic dolomitic bedrock of the catchment. This eutrophic lake is episodically restricted and characterized by alkaline waters with a fluctuating high Mg/Ca ratio. The maximum extension of the Holocene shoreline coincides with evidence of a lake stabilization level corresponding to the outflow of the lake through a wadi. Lakeshore terrace sediments deposited on an alluvial fan siltstone during the past ca 2500 cal yr bp comprise four main facies: a littoral crust, palaeosols, palustrine silts and charophyte tufas, which reflect different environments from the shoreline toward the deeper water. In the more distal parts, the charophyte tufas display a well‐expressed lamination punctuated by the development of microstromatolites on algae thalli. The mineralogical composition of the carbonates is linked to the facies. While the charophyte tufas are characterized by a relatively high content in aragonite, in addition to low‐Mg calcite, the littoral crust is mainly composed of magnesite. This pattern is related to the evolving chemistry of water due to the influence of charophyte proliferation during dry summers. Calcium‐carbonate precipitation on algae thalli (both bioinduced and microbially mediated) progressively induces an increase in the Mg/Ca ratio of the lake water, while the capillary evaporation of shallow ground waters causes precipitation of a magnesite precursor on the shoreline, producing magnesite during early diagenesis. This effect is characteristic of two episodes: part of the Roman Warm Period and the beginning of the Dark Age Cold Period. The carbonate mineralogy of the different depositional sequences at Afourgagh indicates lake‐level and water‐chemistry fluctuations under a climatic influence. Therefore, among other regional records, the Lake Afourgagh sedimentary record provides useful evidence for reconstructing these environmental changes.  相似文献   

6.
Seventy-six samples of formation waters were collected from oil wells producing from the Aux Vases or Cypress Formations in the Illinois Basin. Forty core samples of the reservoir rocks were also collected from the two formations. Analyses of the samples indicated that the total dissolved solids content (TDS) of the waters ranged from 43,300 to 151,400 mg/L, far exceeding the 35,400 mg/L of TDS found in typical seawater. Cl-Br relations suggested that high salinities in the Aux Vases and Cypress formation waters resulted from the evaporation of original seawater and subsequent mixing of the evaporated seawater with concentrated halite solutions. Mixing with the halite solutions increased Na and Cl concentrations and diluted the concentration of other ions in the formation waters. The elemental concentrations were influenced further by diagenetic reactions with silicate and carbonate minerals. Diagenetic signatures revealed by fluid chemistry and rock mineralogy delineated the water-rock interactions that took place in the Aux Vases and Cypress sandstones. Dissolution of K-feldspar released K into the solution, leading to the formation of authigenic illite and mixed-layered illite/smectite. Some Mg was removed from the solution by the formation of authigenic chlorite and dolomite. Dolomitization, calcite recrystallization, and contribution from clay minerals raised Sr levels significantly in the formation waters. The trend of increasing TDS of the saline formation waters with depth can be explained with density stratification. But, it is difficult to explain the combination of the increasing TDS and increasing Ca/Na ratio with depth without invoking the controversial 'ion filtration' mechanism.  相似文献   

7.
The calcretes in the Thar desert occur in a variety of settings, including the piedmonts, sheetwash aggraded plains; and this study adds calcretes in regolith and colluvio-alluvial plains to the group of settings in which calcretes occur in the region. Field logs, morphological details and analytical data such as petrographic, cathodoluminescence and geochemical characteristics are described along with a discussion on their implications. Sand dunes and sandy plains dating to < 20 ka have weakly developed calcretes. The better-developed calcrete horizons occur in piedmonts, interdunes or in areas that have sufficient groundwater. Deep sections in the region show phases of calcrete development in aeolian sand aggradation at ∼ 150, ∼ 100, ∼ 60 and 27–14 ka. The extensive sheetwash plains have mature calcretes and date to mid-Pleistocene. Our studies indicate that these calcretes represent a hybrid process, where carbonate enrichment of the originally calcareous host occurred due to periodically raised groundwaters, and its differentiation into nodules occurred under subaerial environment i.e., after recession of groundwater. Deep sections also show a stack of discrete calcretes that developed in individual aggradation episodes with hiatuses as indicated by ESR dating results. Nodules display a multiplicity of carbonate precipi tation events and internal reorganization of calcitic groundmass. The process is accompanied by degradation and transformation of unstable minerals, particularly clays and with a neosynthesis of palygorskite. The ancient calcretes are dated from the beginning of the Quaternary to ∼ 600 ka and show more evolved morphologies marked by brecciation, dissolution, laminar growth on brecciated surfaces, pisolites and several generations of re-cementation. Mica/chlorite schists and such other rocks are particularly vulnerable to replacement by carbonate. In an extreme case, replacement of quartzose sandstone was observed also. The presence of stretches of alluvio-colluvial plains in an area presently devoid of drainage bespeaks of occasional high-energy fluvial regime, under a semi-arid climate. The mid-Pleistocene period saw a shift towards more arid climate and this facilitated sheetwash aggradation. Finally, during the late Pleistocene, aggradation of aeolian sands indicated a progressively drier climate. However, this does not find its reflection in stable isotope data. The amount of carbonate in the form of calcretes is substantial. The present studies indicate that aeolian dust or rainwater are minor contributors to the carbonate budget. A more important source was provided by the pre-existing calcretes in the sheetwash aggraded plains and detrital carbonate in the aeolian sediments. The original source of carbonate in the region, however, remains unresolved and will need further investigations. Electron spin resonance protocols for the dating of calcretes were developed as a part of this study and the results accorded well with geological reasoning  相似文献   

8.
通过钻井岩心观察及室内测试分析等方法,对江汉盆地江陵凹陷南缘古新统沙市组四段含盐岩系的沉积特征进行了研究.该时期研究区盐湖的特点是:成盐多期次、沉积连续、淡化—成化周期性交替,因而成为恢复古气候和古环境的重要研究对象.该区沙市组四段盐层间的层段由非砂岩组成,主要由单层厚度为几毫米至几十厘米、累积厚度达几十厘米至几米的含...  相似文献   

9.
The Mg/Ca ratio of seawater has varied significantly throughout the Phanerozoic Eon, primarily as a function of the rate of ocean crust production. Specimens of the crustose coralline alga Neogoniolithon sp. were grown in artificial seawaters encompassing the range of Mg/Ca ratios shown to have existed throughout the Phanerozoic. Significantly, the coralline algae’s skeletal Mg/Ca ratio varied in lockstep with the Mg/Ca ratio of the artificial seawater. Specimens grown in seawater treatments formulated with identical Mg/Ca ratios but differing absolute concentrations of Mg and Ca exhibited no significant differences in skeletal Mg/Ca ratios, thereby emphasizing the importance of the ambient Mg/Ca ratio, and not the absolute concentration of Mg, in determining the Mg/Ca ratio of coralline algal calcite. Specimens grown in seawater of the lowest molar Mg/Ca ratio (mMg/Ca = 1.0) actually changed their skeletal mineralogy from high-Mg (skeletal mMg/Ca > 0.04) to low-Mg calcite (skeletal mMg/Ca < 0.04), suggesting that ancient calcitic red algae, which exhibit morphologies and modes of calcification comparable to Neogoniolithon sp., would have produced low-Mg calcite from the middle Cambrian to middle Mississippian and during the middle to Late Cretaceous, when oceanic mMg/Ca approached unity. By influencing the original Mg content of carbonate facies in which these algae have been ubiquitous, this condition has significant implications for the geochemistry and diagenesis of algal limestones throughout most of the Phanerozoic. The crustose coralline algae’s precipitation of high-Mg calcite from seawater that favors the abiotic precipitation of aragonite indicates that these algae dictate the precipitation of the calcitic polymorph of CaCO3. However, the algae’s nearly abiotic pattern of Mg fractionation in their skeletal calcite suggests that their biomineralogical control is limited to polymorph specification and is generally ineffectual in the regulation of skeletal Mg incorporation. Therefore, the Mg/Ca ratio of well-preserved fossils of crustose coralline algae, when corrected for the effect of seawater temperature, may be an archive of oceanic Mg/Ca throughout the Phanerozoic. Magnesium fractionation algorithms that model algal skeletal Mg/Ca as a function of seawater Mg/Ca and temperature are presented herein. The results of this study support the empirical fossil evidence that secular variation of oceanic Mg/Ca has caused the mineralogy and skeletal chemistry of many calcifying marine organisms to change significantly over geologic time.  相似文献   

10.
Earlier interpretations of textural alteration affecting Great Salt Lake ooids have greatly influenced concepts of ooid diagenesis. Scanning electron microscope study shows, however, that the coarse radial aragonite rays are depositional, that no recrystallization of pellet cores has occurred, and that Great Salt Lake ooids have not suffered noticeable diagenesis. As suggested by Kahle (1974), radial texture in ancient calcitic ooids is probably mainly original, not diagenetic. Retention of such fine textures has been attributed to organic matter (since found to be equivalent in modern skeletal and non-skeletal grains) or to paramorphic replacement (proposed for non-skeletal grains whose original aragonite mineralogy was only inferred from modern analogs). Pleistocene ooids known to have been aragonite alter like aragonite shells to coarse neomorphic calcite, often with aragonite relics. The striking uniformity of that coarse texture in neomorphic calcite replacing known skeletal aragonites throughout the geologic record has been noted for over 100 years. In contrast, Mississippian ooids retain fine texture as do calcite layers of coexisting gastropods, but unlike the strongly altered aragonite layers of these same gastropods. Therefore, inferences of original aragonitic mineralogy of ancient non-skeletal carbonate grains (including muds) which are now calcite but retain fine texture appear unwarranted, as do assumptions of differential diagenetic behaviour of ancient aragonitic skeletal and non-skeletal grains. Accordingly, modern depositional environments of marine ooids and carbonate muds must be rejected as chemically unrepresentative of comparable ancient environments. It is inferred that ancient non-skeletal carbonates were originally predominantly or exclusively calcite because of an earlier lower oceanic Mg/Ca ratio (<2/1) which altered progressively to values favouring aragonite (modern Mg/Ca value = 5/1). Major influencing factors are: selective removal of calcium by planktonic foraminifers and coccolithophorids since Jurassic-Cretaceous time and by abundant younger, Mg-poor aragonite skeletons and an erratic trend toward decreasing dolomite formation (decreasing removal of oceanic Mg). The change to aragonite dominance over calcite for non-skeletal carbonates was probably during early to middle Cenozoic time.  相似文献   

11.
Ana M. 《Earth》2003,60(3-4):261-298
Interest in palustrine carbonates and calcretes has increased over the last 20 years since they contain significant environmental information. Much of the work performed in this area has focused on either of two types of terrestrial carbonate—palustrine carbonates or calcretes (pedogenic and groundwater)—yet their simultaneous study shows there may be a gradual transition from one form to the other, revealing the interplay between pedogenic, sedimentary, and diagenetic processes. Three main factors control the formation of these carbonates: the position of the water table, the host rock, and the period of sub-aerial exposure. In pedogenic calcretes, precipitation of carbonate takes places mostly in the vadose zone above the water table, and within a previous host rock or sediment. In groundwater calcretes, the precipitation of carbonate also occurs within a previous host rock and around the groundwater table. In palustrine carbonates, however, the precipitation of lime mud occurs in a lacustrine water body. Palustrine carbonates necessarily form on previous lacustrine mud, whereas both types of calcretes may form on any type of sediment or soil. The sub-aerial exposure time needed to form palustrine carbonates may by relatively short (even a season), whereas pedogenic calcretes need more time (several years to millions of years). Groundwater calcretes do not form on the topographic surfaces, so there is no need of sub-aerial exposure. However, stable surfaces favour the development of thick groundwater calcretes. Small fluctuations in the water table cause gradual transitions of these three types of terrestrial carbonates and the subsequent mixture of their characteristic features, causing difficulties in the interpretation of these carbonates.

The formation of these carbonates is controlled by palaeoenvironmental factors. Both commonly form in semi-arid climates. Arid climates are also suitable for calcretes, but sub-humid conditions are more suitable for palustrine carbonates. More indications of climatic conditions may be obtained through the analysis of the δ18O content of both calcretes and palustrine carbonates, and from the depth of the horizon containing carbonate nodules in pedogenic calcretes. Vegetation is also important in the formation of these types of carbonates. Data on the prevailing vegetation can be obtained from the analysis of the micro and macrofabric as well as from the δ13C signal of the primary carbonates, which, in pedogenic carbonates, has also been used to estimate atmospheric pCO2 during the Phanerozoic. These terrestrial carbonates are widely distributed on floodplains and distal areas of alluvial basins. Their presence and characteristics can be used as indicators of aggradation, subsidence or accommodation rates, and therefore as indicators of different tectonic regimes.

Even though the study of these carbonates has notably increased in recent years, much less is known about them than about marine carbonates. Presently, there is much emphasis on obtaining a general model for sequence stratigraphy in terrestrial basins, with a need to include the carbonates analysed in this paper.  相似文献   


12.
鲕粒原生矿物识别及对海水化学成分变化的指示意义   总被引：1，自引：0，他引：1  
李飞  武思琴  刘柯 《沉积学报》2015,33(3):500-511
鲕粒是碳酸盐沉积过程中一类非常特殊的颗粒类型, 为研究当时的沉积背景、水动力条件、气候环境, 甚至储层特征提供了重要线索。然而, 鲕粒的矿物组成及控制因素问题, 长期受到忽视。组成鲕粒的原生矿物类型在地质历史时期呈周期性变化, 在显生宙表现为三个以文石和高镁方解石占主导的时期以及两个以低镁方解石占主导的时期, 这也被称作“文石海”和“方解石海”时期。原生矿物的组成, 制约着鲕粒的纹层结构、保存程度以及成岩特征, 还蕴含着海水化学成分变化的线索。鲕粒原生矿物识别主要依据:①原生纹层结构;②保存程度;③微量元素浓度, 尤其是Sr-Mg的浓度。文石质鲕粒受文石不稳定性的影响, 原生结构保存程度较差;一般保存有典型的文石残余纹层结构(例如砖砌结构、溶解变形结构以及偏心结构等);在封闭成岩环境下原生矿物为文石质的鲕粒Sr浓度往往大于2 000 ppm;纹层结构主要为切线状(占主导)和放射状。方解石质鲕粒包括低镁方解石和高镁方解石两种类型:低镁方解石为稳定矿物, 原生结构一般保存良好。尽管高镁方解石也为亚稳定矿物, 但成岩转换后的保存程度好于文石。两者Sr含量一般均低于1 000 ppm, Mg含量一般在0~20 mol % MgCO3(两者以4 mol % MgCO3为界)。高镁方解石受成岩作用影响, 在纹层中往往保留有微粒白云石包裹体;海相地层中保存的方解石质鲕粒为放射状或同心-放射状结构。另外还存在一类由两种矿物共同构成的双矿物鲕粒, 可以通过分析两类纹层在结构和保存特征上的差异进行区分。鲕粒原生矿物成分随时间的波动变化受到海水化学条件, 尤其是Mg/Ca比值, 大气二氧化碳分压以及碳酸盐饱和度的控制。Mg/Ca比值的波动决定着鲕粒原生矿物类型的长期变化规律。一些突发性事件可能会扰动(区域)短时间尺度下鲕粒原生矿物的组成, 造成鲕粒原生矿物的转换。通过研究碳酸盐鲕粒原生矿物特征以及控制因素进而了解海水的化学特征, 是独立于古生物学和地球化学分析之外的一种较为可靠的沉积学方法。  相似文献   

13.
利用富钴结壳碳酸盐基岩有孔虫矿物标型重建古海洋温度   总被引：1，自引：0，他引：1  
重建古海洋海表温度(SST),是研究地质历史时期气候变化控制过程的关键。组成有孔虫化石的矿物Mg/Ca值是海水温度的可靠代用指标,是重建古海洋SST的一个非常好的手段。麦哲伦海山区的富钴结壳和基岩中普遍存在有孔虫化石,这对重建该区的SST有重要意义。利用LA-ICP-MS测得西太平洋麦哲伦海山区富钴结壳碳酸盐基岩中8颗浮游有孔虫化石Globigerinoides sacculifer的Mg/Ca值为3.84±0.36(mmol/mol),通过线性公式:T(℃)=2.898Mg/Ca(mmol/mol)+13.76及已有的定年数据,得到0.91Ma±西太平洋麦哲伦海山区海表温度为24.9+1.1/-1.0℃,未能检索到前人关于该区0.91Ma±前海表温度数据。  相似文献   

14.
This study formulates a comprehensive depositional model for hydromagnesite–magnesite playas. Mineralogical, isotopic and hydrogeochemical data are coupled with electron microscopy and field observations of the hydromagnesite–magnesite playas near Atlin, British Columbia, Canada. Four surface environments are recognized: wetlands, grasslands, localized mounds (metre‐scale) and amalgamated mounds composed primarily of hydromagnesite [Mg5(CO3)4(OH)2·4H2O], which are interpreted to represent stages in playa genesis. Water chemistry, precipitation kinetics and depositional environment are primary controls on sediment mineralogy. At depth (average ≈ 2 m), Ca–Mg‐carbonate sediments overlay early Holocene glaciolacustrine sediments indicating deposition within a lake post‐deglaciation. This mineralogical change corresponds to a shift from siliciclastic to chemical carbonate deposition as the supply of fresh surface water (for example, glacier meltwater) ceased and was replaced by alkaline groundwater. Weathering of ultramafic bedrock in the region produces Mg–HCO3 groundwater that concentrates by evaporation upon discharging into closed basins, occupied by the playas. An uppermost unit of Mg‐carbonate sediments (hydromagnesite mounds) overlies the Ca–Mg‐carbonate sediments. This second mineralogical shift corresponds to a change in the depositional environment from subaqueous to subaerial, occurring once sediments ‘emerged’ from the water surface. Capillary action and evaporation draw Mg–HCO3 water up towards the ground surface, precipitating Mg‐carbonate minerals. Evaporation at the water table causes precipitation of lansfordite [MgCO3·5H2O] which partially cements pre‐existing sediments forming a hardpan. As carbonate deposition continues, the weight of the overlying sediments causes compaction and minor lateral movement of the mounds leading to amalgamation of localized mounds. Radiocarbon dating of buried vegetation at the Ca–Mg‐carbonate boundary indicates that there has been ca 8000 years of continuous Mg‐carbonate deposition at a rate of 0·4 mm yr?1. The depositional model accounts for the many sedimentological, mineralogical and geochemical processes that occur in the four surface environments; elucidating past and present carbonate deposition.  相似文献   

15.
The influence of the pedogenic and climatic contexts on the formation and preservation of pedogenic carbonates in a climosequence in the Western Ghats (Karnataka Plateau, South West India) has been studied. Along the climosequence, the current mean annual rainfall (MAR) varies within a 80 km transect from 6000 mm at the edge of the Plateau to 500 mm inland. Pedogenic carbonates occur in the MAR range of 500-1200 mm. In the semi-arid zone (MAR: 500-900 mm), carbonates occur (i) as thick hardpan calcretes on pediment slopes and (ii) as nodular horizons in polygenic black soils (i.e. vertisols). In the sub-humid zone (MAR: 900-1500 mm), pedogenic carbonates are disseminated in the black soil matrices either as loose, irregular and friable nodules of millimetric size or as indurated botryoidal nodules of centimetric to pluricentimetric size. They also occur at the top layers of the saprolite either as disseminated pluricentimetric indurated nodules or carbonate-cemented lumps of centimetric to decimetric size.Chemical and isotopic (87Sr/86Sr) compositions of the carbonate fraction were determined after leaching with 0.25 N HCl. The corresponding residual fractions containing both primary minerals and authigenic clays were digested separately and analyzed. The trend defined by the 87Sr/86Sr signatures of both labile carbonate fractions and corresponding residual fractions indicates that a part of the labile carbonate fraction is genetically linked to the local soil composition. Considering the residual fraction of each sample as the most likely lithogenic source of Ca in carbonates, it is estimated that from 24% to 82% (55% on average) of Ca is derived from local bedrock weathering, leading to a consumption of an equivalent proportion of atmospheric CO2. These values indicate that climatic conditions were humid enough to allow silicate weathering: MAR at the time of carbonate formation likely ranged from 400 to 700 mm, which is 2- to 3-fold less than the current MAR at these locations.The Sr, U and Mg contents and the (234U/238U) activity ratio in the labile carbonate fraction help to understand the conditions of carbonate formation. The relatively high concentrations of Sr, U and Mg in black soil carbonates may indicate fast growth and accumulation compared to carbonates in saprolite, possibly due to a better confinement of the pore waters which is supported by their high (234U/238U) signatures, and/or to higher content of dissolved carbonates in the pore waters. The occurrence of Ce, Mn and Fe oxides in the cracks of carbonate reflects the existence of relatively humid periods after carbonate formation. The carbonate ages determined by the U-Th method range from 1.33 ± 0.84 kyr to 7.5 ± 2.7 kyr and to a cluster of five ages around 20 kyr, i.e. the Last Glacial Maximum period. The young occurrences are only located in the black soils, which therefore constitute sensitive environments for trapping and retaining atmospheric CO2 even on short time scales. The maximum age of carbonates depends on their location in the climatic gradient: from about 20 kyr for centimetric nodules at Mule Hole (MAR = 1100 mm/yr) to 200 kyr for the calcrete at Gundlupet (MAR = 700 mm/yr, Durand et al., 2007). The intensity of rainfall during wet periods would indeed control the lifetime of pedogenic carbonates and thus the duration of inorganic carbon storage in soils.  相似文献   

16.
Euhedral quartz and albite crystals are common in Devonian (Givetian-Frasnian) shallow-marine shelf carbonates from the Belgian Ardennes. Several features such as morphology, the presence of carbonate inclusions, inversion temperatures and occurrence in the insoluble residues of stylolitic surfaces indicate that these crystals have developed authigenically. Oxygen isotope ratios point to an intermediate deep burial realm of origin at temperatures of 60–90°C. The predominance of illite and the almost total absence of smectite clay minerals is interpreted as an indication that illitization produced the silica needed for authigenesis. The mineral composition of inclusions indicates that the carbonate host rock must have consisted of low-Mg calcite already at the time of authigenesis. These inclusions represent an earlier diagenetic stage than the present carbonate rock, since they were protected from further diagenetic alteration by the surrounding quartz. The calcite inclusions display a higher Sr/Ca and Mg/Ca ratio than the carbonate host-rock. Because neomorphic diagenesis of the carbonate continued after silicate authigenesis, the contents of Mg and Sr in the calcite of the host carbonate are even lower. The authigenic feldspar mineralogy seems to be determined by the composition of the host-sediment.  相似文献   

17.
陆现彩  张文兰 《沉积学报》1998,16(1):120-125
以东营凹陷沙四段上部烃源岩为研究对象,利用电子探针微区测试技术,对同生、成岩及成岩期后不同阶段碳酸盐矿物进行了系统分析,揭示出不同古地理位置碳酸盐成分的三种变化情况,即Mg/Ca比值①由高到低,②一直保持很高,成岩期后降低,和③由低到高,反映了不同层段从沉积到成岩直至成岩期后水体或孔隙流体盐度的三种变化历程,进而确定了该凹陷中心区域烃源岩成岩过程中处于高盐度介质环境中,对于分析该区油气生成条件具有重要意义。本文的研究思路和方法对于其它地区的类似工作也有一定借鉴意义。  相似文献   

18.
The non-marine Campins Basin developed in the Oligocene, during a period of early rifting of the Catalan Coastal Ranges. Lacustrine deposits, interbedded between two alluvial units, comprise shallow and deep lacustrine facies. The lower, shallow lacustrine facies are made up of microbialite buildups and thin limestone beds. In the studied area, these facies are overlain by deep lacustrine facies which consist of alternations of several, metre-thick carbonate- and mudstone-dominated intervals. In addition to calcite, which is characteristic of the shallow lacustrine facies, aragonite and abundant dolomite are present in the deep lacustrine facies. This mineralogical change in the sequence reflects an overall increase in the Mg/Ca ratio of the lake waters. The deep lacustrine sequences are interpreted as having formed in a hydrologically closed basin that was subject to changes in the Mg/Ca ratio of the water, probably related to variations in the evaporation/precipitation rate. The sedimentological, mineralogical and isotopic characteristics of the Campins Basin dolomites suggest that, in general, they are primary in origin. The stable isotope data show an approximate covariance between δ13C and δ18O in the lower shallow lacustrine carbonates (calcite) which suggests that they formed during the onset of closure of the lake. The δ13C and δ18O values of the deep lacustrine carbonates display three different clusters that are roughly related to the carbonate mineralogy. Normalisation with respect to calcite of the isotopic compositions of dolomite and aragonite from the deep lacustrine carbonates allows the integration of all these isotope values into one covariant trend. The sequential appearance of different carbonate minerals and the isotopic covariant trend may indicate an overall evaporative concentration of the lake waters. The change in slope of the covariant trend for the isotope values between the shallow and the deep lacustrine carbonates might reflect the change in the waterbody morphology recorded in the basin fill sequence.  相似文献   

19.
This study investigates the conditions of occurrence and petrographic characteristics of low‐Mg calcite (LMC) from cold seeps of the Gulf of Mexico at a water depth of 2340 m. Such LMC mineral phases should precipitate in calcite seas rather than today's aragonite sea. The 13C‐depleted carbonates formed as a consequence of anaerobic oxidation of hydrocarbons in shallow subsurface cold seep environments. The occurrence of LMC may result from brine fluid flows. Brines are relatively Ca2+‐enriched and Mg2+‐depleted (Mg/Ca mole ratio <0.7) relative to seawater, where the Mg/Ca mole ratio is ~5, which drives high‐Mg calcite and aragonite precipitation. The dissolution of aragonitic mollusk shells, grains and cements was observed. Aerobic oxidation of hydrocarbons and H2S is the most likely mechanism to explain carbonate dissolution. These findings have important implications for understanding the occurrence of LMC in deep water marine settings and consequently their counterparts in the geological record.  相似文献   

20.
Siderite (FeCO3) is a widespread minor diagenetic mineral in clastic sedimentary basins. Although eodiagenetic authigenesis of siderite is well-known, siderite formed during burial diagenesis shows habits and chemical compositions that are poorly understood. This study tests the hypothesis that diagenetic siderite cements in sandstones in the Scotian Basin, offshore eastern Canada, show systematic variability in chemistry and habit that is a response to recrystallization and changing composition of basinal fluids. Mineral textures were determined from backscattered electron images, and chemistry mostly from electron microprobe analyses. Five chemical types of siderite are identified using k-means cluster analysis, based on the amount of substitution of Ca, Mg and Mn for Fe. Eodiagenetic microcrystalline coated grains, concretions and intraclasts in sandstones are principally Fe-rich siderite and locally have recrystallised to blocky equant crystals. Mesodiagenetic Mg-rich siderite partly replaced these equant crystals and also framework mica and K-feldspar grains, showing textural evidence for coupled dissolution–reprecipitation. Slender Mg-rich siderite rhombs (lozenges, bladed or wheat-seed siderite) have precipitated before and after the formation of quartz overgrowths in geochemical microenvironments. Magnesium substitution reflects Mg-rich formation waters resulting from smectite to illite conversion. Equivalent Ca-rich siderite occurs where sandstones overlie a Jurassic carbonate bank. Late Mn-rich siderite has complex textures resembling those of Mississippi-Valley type ores, with spheroidal rims, a honeycomb-like mesh and concentric infill around secondary pores. It also occurs in veins or replacing intraclasts, post-dating late ferroan-calcite cements in sandstones that show strong dissolution by hot basinal brines. The Ca, Mg and Mn content of diagenetic siderite, coupled with textural evidence for recrystallization, can thus be used to track changes in ambient formation fluids. Siderite habits and chemistry described from the Scotian Basin are found in many clastic basins, suggesting that the observed recrystallization textures and variation in chemical type are of broad application.  相似文献   

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