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1.
扬子地台上震旦统-下古生界白云岩广泛发育，是最重要的碳酸盐岩储集层.目前对下扬子地区白云岩的研究程度较低，严重制约了对该区白云岩储层性能的深化认识和油气勘探工作.研究以南京地区为例，通过对该区上震旦统-下古生界白云岩进行系统的岩石学、主量和微量元素、碳-氧同位素及稀土元素分析，确定了白云岩的类型及成因.结果表明：研究区发育泥晶白云岩、粉-细晶白云岩、细晶白云岩、中晶白云岩4种白云岩类型.上震旦统泥晶白云岩具有较高的Mg含量和较低的Fe、Mn、Sr元素含量，δ18O平均值高达0.2‰，形成温度近于地表温度，盐度指数明显高于海水，∑REE值约为28×10-6,δCe和δEu呈负异常，平均分别为0.867和0.917，稀土元素配分模式与海相灰岩类似，为近地表强蒸发浓缩海水流体环境下准同生白云石化成因；中寒武统粉-细晶白云岩晶体具有雾心亮边和环边状结构，Mg、Fe、Mn元素含量和稀土元素特征与泥晶白云岩类似，盐度指数较高，说明有相似的海水流体性质，δ18O值介于-2.5‰～-6.5‰，为浅埋藏环境下渗透回流白云石化成因；上寒武统... 相似文献
2.
川东北地区下三叠统飞仙关组为浅海碳酸盐岩夹泥页岩与蒸发岩序列,而在碳酸盐岩台地边缘通常发育一些白云石化的鲕粒滩。这些鲕粒滩白云岩储集层是川东北地区主要的产气层,一些学者认为该套白云岩为大气淡水与海水的混合水白云石化成因,另外一些学者将其视为回流—渗透白云石化成因。飞仙关组鲕粒滩白云岩稳定同位素氧值一般为-6.73‰～-3.65‰(PDB),平均值为-4.89‰(PDB)（罗家寨地区为-10.81‰(PDB)）,稳定同位素碳值一般为+0.57‰～+3.00‰(PDB)。对基质和孔洞中充填的鞍状白云石和亮晶白云石胶结物而言,稳定同位素87Sr/86Sr值为0.70735～0.70800。这些有关鲕粒滩白云岩的数据表明白云石化作用是在埋藏条件下进行的。在测定流体包裹体的均一化温度后,计算出白云石化流体稳定同位素氧成分(δ18O白云石-δ18O水=［3.2×106 T-2］-1.5,来自 Friedman 和 ONeil（1977）),其平均值约为+4‰(SMOW)。根据流体稳定同位素氧、碳成分与海水蒸发时流体盐度的正相关性,计算出流体δD平均值约为+25‰(SMOW)。流体包裹体盐度测定表明,白云石化流体是一种超盐度卤水,其盐度是海水的数倍,白云石化的温度为90～130℃。由于下三叠统鲕粒滩白云岩的稳定同位素氧和碳成分与上二叠统生物礁白云岩的稳定同位素氧和碳成分类似,因此,它们的白云石化流体很可能是同一来源。然而,这一结论还有待于进一步研究。 相似文献
3.
通过对鄂尔多斯盆地马家沟组五段5亚段白云岩的岩石学和地球化学研究表明,主要岩性有泥晶白云岩、泥粉晶白云岩和粉晶白云岩等三类。泥晶白云岩类为泥晶结构,阴极发光为暗红光,白云石有序度低;Na、K和Sr值较高;δ~(13)C平均-1.23‰,δ~(18)O平均-7.59‰,锶同位素平均值0.709 81,形成于闭塞局限、盐度相对较高的环境,由准同生白云石化作用所形成,并发育少量晶间微孔。泥粉晶白云岩类为泥晶—细粉晶结构,不发光或发极暗的红光,白云石有序度0.75;常量元素、微量元素大幅降低;δ~(13)C和δ~(18)O的平均值分别是-0.43‰和-7.29‰,锶同位素平均值0.709 36,由准同生后回流渗透白云石化作用所形成,并发育晶间孔。粉晶白云岩不发光或发极暗红光,白云石有序度0.81;常量元素、微量元素有明显的突变;δ~(13)C和δ~(18)O平均值分别为-0.65‰和-6.46‰,锶同位素平均值0.709 67,由埋藏白云石化作用所形成,并发育晶间扩溶孔或溶蚀孔。 相似文献
4.
加拿大阿尔伯达省西部上泥盆统凯恩组白云岩的成因 总被引：1，自引：0，他引：1
加拿大阿尔伯达省西部上泥盆统凯恩组主要由粉晶白云岩和细晶白云岩组成，另外还常见一种充填溶蚀孔洞的亮晶白云石。粉晶白云岩纹理、泥裂和鸟眼等构造发育，其δ＾１３Ｃ为＋１．０‰－＋３．０‰，δ＾１８Ｏ为－６．０‰－－４．３‰，为潮坪上混合水白云化形成。细晶白云岩分布于假整合面之下，其δ＾１３Ｃ为＋０．２‰－＋２．９‰，δ＾１８Ｏ为－６．９‰－－４．６‰，也是混合水白云化的产物。亮晶白云石洁净明亮、晶粒粗 相似文献
5.
灯影组白云岩是四川盆地超深层油气勘探的重点领域,但目前人们对该套白云岩成因争议仍较大,且缺乏系统研究.通过对四川盆地灯影组白云岩C-O-Sr同位素和稀土元素数据的系统分析来研究白云石化流体的化学性质和成因,进而约束白云岩的差异性成因机制.研究表明：(1)灯影组白云岩碳同位素值较均一,δ13C值基本分布在0‰～+5.0‰之间,而氧同位素值变化较大.近地表环境基质白云岩和早期白云石胶结物δ18O均大于-8.0‰,埋藏环境白云石胶结物δ18O均小于-8.0‰,而热液白云石化胶结物δ18O均小于-10.0‰.(2)基质白云岩和早期白云石胶结物具有与同期海水相似的87Sr/86Sr值(0.708～0.709),指示其继承于海水流体;而埋藏环境白云石胶结物87Sr/86Sr比值明显大于同期海水,指示其为地层流体和深部热液流体来源.(3)灯影组白云岩稀土元素均亏损轻稀土元素、富集重稀土元素.基质白云岩和早期白云石胶结物可见Ce负异常、未见Eu明显异... 相似文献
6.
上新世最重要的古气候事件就是北极冰盖的形成和扩张（3.2—2.5Ma）。根据北极冰盖的形成过程,文中将上新世—早更新世（4.5—1.6Ma）西太平洋暖池核心区ODP807A孔2个浮游有孔虫属种Globigerinoides ruber和Pulleniatina obliquiloculata的δ18O（氧同位素）、δ13C（碳同位素）记录数据细分为3个阶段：形成前（4.5—3.2Ma）、形成中（3.2—2.5Ma）和形成后（2.5—1.6Ma）。研究结果表明,北极冰盖形成以来,G.ruber和P.obliquiloculata的 δ18O值均呈增大趋势;北极冰盖形成中,G.ruber 的δ18O值基本不变,P.obliquiloculata的 δ18O值略增大,反映出西太平洋暖池次表层海水受北极冰盖形成的影响更甚;Δδ18O（P-G）（G.ruber和P.obliquiloculata的 δ18O 的差值）反映出温跃层无明显变化,受北极冰盖形成影响微弱。根据用Ma/Ca值得到的ODP806站SST值（Wara et al.,2005）以及用UK′37得到的东太平洋ODP847站SST值数据（Herbert and Laura,2010）,对北极冰盖形成以来东西太平洋古海洋学演化进行比较发现：冰盖形成以来东西赤道太平洋海水表层温度均有所下降,且东太平洋降温幅度更大;对比同时期的西太平洋ODP807A孔Δδ18O（P-G）与东太平洋ODP847站Δδ18O（T-S）的变化趋势,发现东太平洋温跃层变浅,表明受北极冰盖形成和扩张的影响,东西太平洋温跃层深度梯度增大。对比ODP807A孔与南海南部1143站、南海北部1148站G.ruber的 δ18O 和δ13C记录,揭示西太平洋边缘海如南海北部和南部受北极冰盖形成的影响有所不同,北部的表层海水温度和生产力水平受冰盖形成的影响更加明显。 相似文献
7.
塔里木盆地柯坪地区中寒武统藻白云岩去白云岩化研究 总被引：1，自引：0，他引：1
对塔里木盆地柯坪地区中寒武统去白云岩化现象进行了研究。去白云岩化限于渗透性较好的藻白云岩,并且只有靠近含膏层段的藻白云岩才发生去白云岩化。从微观上看,发生去白云岩化的藻灰岩与藻灰云岩含有明显的去白云岩化交代残余,白云石残余呈碎斑状或树枝状。树枝状白云石残余含有大量的方解石包裹体,同时具有较高的Ca/Mg比,为高钙白云石,去白云岩化较彻底,形成藻灰岩;碎斑状白云石残余成分较均一,接近化学计量白云石(Ca/Mg比接近1),去白云岩化程度较弱,形成藻灰云岩。藻灰云岩的δ18O值(平均值为-6.7‰)明显低于邻近的白云岩(平均值为-5.3‰),同时高于藻灰岩(平均值为-9.5‰)。与未发生去白云岩化的藻白云岩相比,藻灰岩与藻灰云岩的孔隙度要明显降低。 相似文献
8.
以黔中地区下奥陶统为例,通过野外剖面观测、实验分析等工作,揭示了白云岩的热液-岩溶改造特征,并探讨了其发育机理。研究区下奥陶统红花园组和桐梓组以白云岩为主,在白云岩构造裂缝和溶蚀孔洞中见白云石、方解石、沥青的充填,具有典型的斑马纹状构造。充填白云石为粗晶粒状的鞍形白云石,具有弯曲晶面和波状消光的特征,阴极发光呈现较强的红色。充填白云石的碳同位素δ~(13)C在-2.2‰~-0.8‰之间,平均值为-1.47‰,氧同位素δ~(18)O在-12.2‰~-7.6‰之间,平均值为-9.4‰,与围岩白云石相比明显偏轻。充填白云石的稀土元素具有典型的Eu正异常特征,δEu最高达91.9。根据地质演化背景和流体作用类型,奥陶系白云岩储层发育过程为:早奥陶世沉积过程中发生同生/准同生白云石化作用;中晚奥陶世至早志留世,受都匀运动影响,白云岩暴露至地表遭受岩溶作用,形成岩溶孔洞型白云岩储层;中泥盆世遭受构造热液进一步对白云岩进行的溶蚀改造,所形成的溶蚀孔洞为天然气的主要储集空间。 相似文献
9.
近期川东南多口钻井在中二叠统茅口组白云岩储层获得了油气突破，但具有很强的非均质性，白云岩化机理不明确，难以预测优质白云岩储层的展布规律。本次研究基于区域地质背景和峨眉山大火成岩省热事件，通过岩石学和地球化学等综合分析，系统总结了不同类型白云岩的特征及成因机理。研究认为：川东南茅口组白云岩以细-中晶白云岩为主，泥-粉晶白云岩和白云石胶结物次之；綦江地区主要发育层状细-中晶白云岩，白云石呈自形-半自形晶，多具有雾心亮边结构和明显的颗粒幻影，阴极发光下晶体内部呈棕色-红色，由内向外过渡为暗红色，细-中晶白云石的δ18OV-PDB、δ13CV-PDB和87Sr/86Sr值均表明白云岩化流体主要为海水，白云石可能为浅埋藏期中等盐度回流渗透白云岩化作用生成，后期经历重结晶或海源流体的热调整改造；泰来地区主要发育斑块状泥-粉晶、细-中晶白云岩以及裂缝内充填的白云石胶结物，原始岩石较致密，晶粒结构不明显，白云石胶结物以具波状消光的鞍形白云石为主，阴极发光下可见多期环带状特... 相似文献
10.
中国南方灯影峡期(晚前寒武纪)是白云岩广泛发育的海洋碳酸盐沉积时期,在灯影组.中部发育从海水直接沉积、沉淀的原生白云岩,目前仍保留其原始组构特征。从40个原生白云石(岩)中测得:泥晶白云石的δ13C值为3.64‰,δ18O值为-1.17‰(n=6);藻白云岩的δ13C值为3.52‰,δ18O值为-1.86‰(n=15);海水纤状白云石胶结物δ13C值为2.90‰,δ18O值为-2.65‰(n=8);海水刃状白云石胶结物的δ13C值为2.96‰,δ18O值为-2.41‰(n=8);泥晶纹层和海水纤状白云石胶结物的δ13C值为2.79‰,δ18O值为-3.13‰。40个岩样的δ13C平均值为3.25‰±0.44‰,δ18O平均值为-2.12‰±0.98‰(均以PDB标准)。对于灯影峡期海相白云岩的原始δ13C和δ18O值,不采用所有样品的平均值,而是采用原生白云石沉积物与海水白云石胶结物δ13C值和δ18O值两个图示分布区重叠部分的最重同位素值,即：δ13C值为4.43‰(PDB标准),δ18O值为-0.62‰(PDB标准),将其作为灯影峡期海洋碳酸盐岩的原始同位素组成。对海水原生白云石胶结物包裹体盐度进行了测定,海水δ18O计算值为2.90‰(SMOW标准),用原始δ18O值计算的原生白云石形成时的海水温度为40.8 ℃。这说明中国南方灯影峡期的海洋为炎热的较高的海水温度环境。 相似文献
11.
Dotan Shaked Gelband Yael Edelman‐Furstenberg Mordechai Stein Abraham Starinsky 《Sedimentology》2019,66(7):2950-2975
The study focuses on the formation of lacustrine dolomite in late Miocene lakes, located at the East Mediterranean margins (Northern Israel). These lakes deposited the sediments of the Bira (Tortonian) and Gesher (Messinian) formations that comprise sequences of dolostone and limestone. Dolostones are bedded, consist of small‐sized (<7 μm), Ca‐rich (52 to 56 mol %) crystals with relatively low ordering degrees, and present evidence for replacement of CaCO3 components. Limestones are comprised of a wackestone to mudstone matrix, freshwater macrofossils and intraclasts (mainly in the Bira Formation). Sodium concentrations and isotope compositions differ between limestones and dolostones: Na = ~100 to 150 ppm; ~1000 to 2000 ppm; δ18O = ?3·8 to ?1·6‰; ?2·0 to +4·3‰; δ13C = ?9·0 to ?3·4‰; ?7·8 to 0‰ (VPDB), respectively. These results indicate a climate‐related sedimentation during the Tortonian and early Messinian. Wet conditions and positive freshwater inflow into the carbonate lake led to calcite precipitation due to intense phytoplankton blooms (limestone formation). Dry conditions and enhanced evaporation led to precipitation of evaporitic CaCO3 in a terminal lake, which caused an increased Mg/Ca ratio in the residual waters and penecontemporaneous dolomitization (dolostone formation). The alternating lithofacies pattern reveals eleven short‐term wet–dry climate‐cycles during the Tortonian and early Messinian. A shift in the environmental conditions under which dolomite formed is indicated by a temporal decrease in δ18O of dolostones and Na content of dolomite crystals. These variations point to decreasing evaporation degrees and/or an increased mixing with meteoric waters towards the late Messinian. A temporal decrease in δ13C of dolostones and limestones and appearance of microbial structures in close association with dolomite suggest that microbial activity had an important role in allowing dolomite formation during the Messinian. Microbial mediation was apparently the main process that enabled local growth of dolomite under wet conditions during the latest Messinian. 相似文献
12.
The stable enrichment of pyrite from magnesite ores in δ34S isotope (from 5.4 to 6.9‰) compared with pyrite from the host (sedimentary and igneous) rocks was established in the classical Satka sparry magnesite ore field. Concretionary segregations of fine-grained pyrite in dolomite are depleted in the heavy sulfur isotope (δ34S, from–9.1 to–5.8‰). Pyrite from dolerite is characterized by δ34S values (–1.1 and 1.7‰) close to the meteorite sulfur. The δ34S values in barite from the underlying dolomite horizon vary in the range of 32.3–41.4‰. The high degree of homogeneity of the sulfur isotope composition in pyrite from magnesite is a result of thermochemical sulfate reduction during the syngenetic crystallization of pyrite and magnesite from epigenetic brines, formed during dissolution of evaporite sulfate minerals at the stage of early catagenesis of the Riphean deposits.
相似文献13.
Dolomitization,gypsum calcitization and silicification in carbonate–evaporite shallow lacustrine deposits 
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下载免费PDF全文 This paper describes and interprets the mineral and facies assemblages that occur in carbonate–evaporite shallow lacustrine deposits, considering the importance of the processes pathway (i.e. dolomitization, gypsum calcitization and silicification). The Palaeogene deposits of the Deza Formation (Almazán Basin, central‐northern Spain) are selected as a case study to determine the variety of physicochemical processes taking place in carbonate–evaporite shallow lakes and their resulting diagenetic features. Dolostones are the predominant lithology and are composed mainly of dolomite with variable amounts of secondary calcite (5 to 50%), which mainly mimic lenticular gypsum (pseudomorphs). Five morphological types of dolomite crystal were identified as follows: dolomite tubes, dolomite cylinders, rhombohedral dolomite, spheroidal and quasi‐rhombohedral dolomite, and cocoon‐shaped dolomite. The dolomite cylinders and tubes are interpreted as the dolomitized cells of a widespread microbial community. The sequence of diagenetic processes started with growth of microlenticular interstitial gypsum in a calcareous mud deposited on the playa margin mudflats, and that sometimes included microbial sediments. Immediately following growth of gypsum, dolomite replaced the original calcite (or possibly aragonite) muds, the microbial community and the gypsum. Partial or total replacement of gypsum by dolomite was related mainly to the biomineralization of endolithic microbial communities on gypsum crystals. Later calcitization took place under vadose, subaerial exposure conditions. The development of calcrete in distal alluvial settings favoured the release of silica and subsequent silicification on the playa margin mudflats. Stable isotope compositions of calcite range from ?9·02 to ?5·83‰ δ13CPDB and ?7·10 to 1·22‰ δ18OPDB; for the dolomite, these values vary from ?8·93 to ?3·96‰ δ13CPDB and ?5·53 to 2·4‰ δ18OPDB. Quartz from the cherts has δ18OSMOW values ranging from 27·1 to 31·1‰. Wide variation and relatively high δ18OSMOW values for dolomite indicate evaporitic and closed hydrological conditions; increased influx of meteoric waters reigned during the formation of secondary calcite spar. 相似文献
14.
Stable isotope evidence for the origin of diagenetic carbonate minerals from the Lower Jurassic Inmar Formation, southern Israel 总被引：1，自引：0，他引：1
The oxygen isotope compositions of diagenetic carbonate minerals from the Lower Jurassic Inmar Formation, southern Israel, have been used to identify porewater types during diagenesis. Changes in porewater composition can be related to major geological events within southern Israel. In particular, saline brines played an important role in late (Pliocene-Pleistocene) dolomitization of these rocks. Diagenetic carbonates included early siderite (δ18OSMOW=+24.4 to +26.5‰δ13CPDB=?1.1 to +0.8‰), late dolomite, ferroan dolomite and ankerite (δ18OSMOW=+18.4 to +25.8‰; δ13CPDB=?2.1 to +0.2‰), and calcite (δ18OSMOW=+21.3 to +32.6‰; δ13CPDB=?4.2 to + 3.2‰). The petrographic and isotopic results suggest that siderite formed early in the diagenetic history at shallow depths. The dolomitic phases formed at greater depths late in diagenesis. Crystallization of secondary calcite spans early to late diagenesis, consistent with its large range in isotopic values. A strong negative correlation exists between burial depth (temperature) and the oxygen isotopic compositions of the dolomitic cements. In addition, the δ18O values of the dolomitic phases in the northern Negev and Judea Mountains are in isotopic equilibrium with present formation waters. This behaviour suggests that formation of secondary dolomite post-dates the tectonic activity responsible for the present relief of southern Israel (Upper Miocene to Pliocene) and that the dolomite crystallized from present formation waters. Such is not the case in the Central Negev. In that locality, present formation waters have much lower salinities and δ18O values, indicating invasion of freshwater, and are out of isotopic equilibrium with secondary dolomite. Recharge of the Inmar Formation by meteoric water in the Central Negev occurred in the Pleistocene, and halted formation of dolomite. 相似文献
15.
PATRICK MEISTER† JUDITH A. MCKENZIE† CRISOGONO VASCONCELOS† STEFANO BERNASCONI† MARTIN FRANK‡ MARCUS GUTJAHR§ DANIEL P. SCHRAG¶ 《Sedimentology》2007,54(5):1007-1032
Early diagenetic dolomite beds were sampled during the Ocean Drilling Programme (ODP) Leg 201 at four reoccupied ODP Leg 112 sites on the Peru continental margin (Sites 1227/684, 1228/680, 1229/681 and 1230/685) and analysed for petrography, mineralogy, δ13C, δ18O and 87Sr/86Sr values. The results are compared with the chemistry, and δ13C and 87Sr/86Sr values of the associated porewater. Petrographic relationships indicate that dolomite forms as a primary precipitate in porous diatom ooze and siliciclastic sediment and is not replacing the small amounts of precursor carbonate. Dolomite precipitation often pre‐dates the formation of framboidal pyrite. Most dolomite layers show 87Sr/86Sr‐ratios similar to the composition of Quaternary seawater and do not indicate a contribution from the hypersaline brine, which is present at a greater burial depth. Also, the δ13C values of the dolomite are not in equilibrium with the δ13C values of the dissolved inorganic carbon in the associated modern porewater. Both petrography and 87Sr/86Sr ratios suggest a shallow depth of dolomite formation in the uppermost sediment (<30 m below the seafloor). A significant depletion in the dissolved Mg and Ca in the porewater constrains the present site of dolomite precipitation, which co‐occurs with a sharp increase in alkalinity and microbial cell concentration at the sulphate–methane interface. It has been hypothesized that microbial ‘hot‐spots’, such as the sulphate–methane interface, may act as focused sites of dolomite precipitation. Varying δ13C values from −15‰ to +15‰ for the dolomite are consistent with precipitation at a dynamic sulphate–methane interface, where δ13C of the dissolved inorganic carbon would likewise be variable. A dynamic deep biosphere with upward and downward migration of the sulphate–methane interface can be simulated using a simple numerical diffusion model for sulphate concentration in a sedimentary sequence with variable input of organic matter. Thus, the study of dolomite layers in ancient organic carbon‐rich sedimentary sequences can provide a useful window into the palaeo‐dynamics of the deep biosphere. 相似文献
16.
Most vein minerals deposited in fractures of the Jialingjiang Formation from Libixia section,Hechan area include a large amount of saddle dolomite and accompanying celestite,calcite and fluorite.This study analyzed the nature,source,evolution of the fluids by plane-light petrography,fluid-inclusion methods,cathodoluminescence images,and stable isotopic compositions.The homogenization temperatures of two-phase aqueous fluid inclusions in dolomite range between100 and 270℃.Combined with theδ~(18)O data,it is suggested that the fluid responsible for the precipitation of fracture fillings haveδ~(18)O values between 10‰and 18‰(relative to SMOW).The saddle dolomite and the accompanying minerals were the result of activity of dense brines at elevated temperatures.Moreover,analysis shows that the fluid was derived from a mixture of marine-derived brine and deeper circulating flow.This fluid was enriched in Sr during diagenesis and formed celestite in fracture and for regional mineralization.Dissolution of saddle dolomite was attributed to the cooling of Mg/Ca-decreased fluids,which may relate to a leaching of gypsum to celestite in surrounding carbonates. 相似文献
17.
QIN Xiwei MA Haizhou ZHANG Xiying CHENG Huaide HAN Jibin LI Yongshou MIAO Weiliang HAI Qingyu 《《地质学报》英文版》2019,93(4):1097-1112
Chemical and isotopic data were measured for 51 leached brine springs in the Changdu-Lanping-Simao Basin (CD-LP-SM), China. The predominance of Cl and Na, saturation indices of carbonate minerals, and Na/Cl and Ca/SO4 ratios of ~1 suggest that halite, sulphate, and carbonate are the solute sources. Integration of geochemical, δ18O, and δD values suggests that springs are mainly derived from meteoric water, ice-snow melt, and water-rock interactions. B concentrations range from 0.18 to 11.9 mg/L, with δ11B values of ?4.37‰ to +32.39‰, indicating a terrestrial source. The δ11B-B relationships suggest B sources of crustal origin (marine carbonates with minor crust-derived volcanics); we did not identify a marine or deep mantle origin. The δ11B values of saline springs (+4.61‰ to +32.39‰) exceed those of hot (?4.37‰ to +4.53‰) and cold (?3.47‰ to +14.84‰) springs; this has contributed to strong water-rock interactions and strong saturation of dissolved carbonates. Conversely, the global geothermal δ11B-Cl/B relationship suggests mixing of marine and non-marine sources. The δ11B-Cl/B relationships of the CD-LP-SM are similar to those of the Tibet geothermal belt and the Nangqen Basin, indicating the same B origin. These differ from thermal waters controlled by magmatic fluids and seawater, suggesting that B in CD-LP-SM springs has a crustal origin. 相似文献
18.
Dolomitization of the Capitan Formation forereef facies (Permian, west Texas and New Mexico): seepage reflux revisited 总被引：5，自引：0，他引：5
Abstract Interpretation of seepage reflux dolomitization is commonly restricted to intervals containing evaporites even though several workers have modelled reflux of mesosaline brines. This study looked at the partially dolomitized forereef facies of the Capitan Formation to test the extent of reflux dolomitization and evaluate the possible role of the near‐backreef mesosaline carbonate lagoon as an alternative source of dolomitizing fluids. The Capitan Formation forereef facies ranges from 10% to 90% dolomite. Most of the dolomite is fabric preserving and formed during early burial after marine cementation, before and/or during evaporite cementation and before stylolitization. Within the forereef facies, dolomite follows depositional units, with debris‐flow and grain‐flow deposits the most dolomitized and turbidity‐current deposits the least. The amount of dolomite increases with stratigraphic age and decreases downslope. Within the reef facies, dolomite is restricted to haloes around fractures and primary cavities except where the reef facies lacks marine cements and, in contrast, is completely dolomitized. This dolomite distribution supports dolomitization by sinking fluids. Oxygen isotopic values for fabric‐preserving dolomite (δ18O = 0·9 ± 1·0‰, N = 101) support dolomitization by sea water to isotopically enriched sea water. These values are closer to the near‐backreef dolomite (δ18O = 2·1 ± 0·7‰, N = 48) than the hypersaline backreef dolomite (δ18O = 3·6 ± 0·9‰, N = 11). Therefore, the fabric‐preserving dolomite is consistent with dolomitization during seepage reflux of mainly mesosaline brines derived from the near‐backreef carbonate lagoon. The occurrence of mesosaline brine reflux in the Capitan Formation has important implications for dolomitization in forereef facies and elsewhere. First, any area with a restricted carbonate lagoon may be dolomitized by refluxing brines even if there are no evaporite facies present. Secondly, such brines may travel significant distances vertically provided permeable pathways (such as fractures) are present. Therefore, the absence of immediately overlying evaporite or restricted facies is not sufficient cause to eliminate reflux dolomitization from consideration. 相似文献
19.
The calcite fossils of the Derbyhaven Beds, Isle of Man, have δ13C values (+ 1·8 PDB) similar to modern, shallow-water marine skeletons, but the δ18O values (?6·1 PDB) are much lighter than modern skeletons. The light oxygen values indicate either re-equilibration with isotopically light water before cementation started, or Carboniferous sea water with δ18O of ?6‰. Aragonite dissolution was followed by precipitation of zoned calcite cement. In this cement, up to six intracrystalline zones, recognized in stained thin sections, show isotopic variation. Carbon varies from + 3-8 to + 1-2‰. and oxygen from ? 2-6 to ? 12-4‰. with decreasing age of the cement. This trend is attributed to increasing temperature and to isotopic evolution of the pore waters during burial. The zoned calcite is sequentially followed by dolomite and kaolinite cements which continue the trend towards light isotopic values. This trend is continued with younger, fault-controlled dolomite, and is terminated by vein-filling calcite and dolomite. The younger calcite, interpreted as a near-surface precipitate from meteoric waters, is unrelated to the older sequence of carbonates and has distinctly different carbon isotope ratios: δ13C ? 6-8‰. 相似文献
20.
Jurassic septarian concretions from NW Scotland record interdependent bacterial, physical and chemical processes of marine mudrock diagenesis 总被引：3，自引：0，他引：3
JAMES P. HENDRY MICHAEL J. PEARSON† NIGEL H. TREWIN‡ ANTHONY E. FALLICK§ 《Sedimentology》2006,53(3):537-565
Septarian concretions in the Staffin Shales Formation (Kimmeridgian, Isle of Skye) allow controls on concretion rheology and septarian cracking to be investigated. Stratabound concretions consist of anhedral ferroan calcite microspar enclosing clay and minor pyrite. Intergranular volumes range from 77% to 88%, and calcite δ13C and δ18O values in most concretion bodies range from ?10·0‰ to ?17·3‰ and +0·3‰ to ?0·6‰ respectively, consistent with rapid and pervasive cementation in marine pore fluids. Septarian rupture occurred during incipient cementation, with a sediment volume reduction of up to 43%. Crack‐lining brown fibrous calcite records pore fluid re‐oxygenation during a depositional hiatus, followed by increasing Fe content and δ13C related to bacterial methanogenesis. Brown colouration results from an included gel‐like polar organic fraction that probably represents bacterially degraded biomass. A new hypothesis for concretion growth and septarian cracking argues that quasi‐rigid ‘proto‐concretions’ formed via binding of flocculated clays by bacterial extracellular polysaccharide substances (EPS). This provided rheological and chemical conditions for tensional failure, subcritical crack growth, volume contraction, calcite nucleation, and incorporation of degraded products into crack‐lining cements. Bacterial decay of EPS and syneresis of host muds provided internal stresses to initiate rupture at shallow burial. Development of septarian (shrinkage) cracks in muds is envisaged to require pervasive in situ bacterial colonization, and to depend on rates of carbonate precipitation versus EPS degradation and syneresis. Subsequent modification of septarian concretions included envelopment by siderite and calcite microspar, hydraulic fracturing associated with Cretaceous shallow burial or Palaeogene uplift; and cementation by strongly ferroan, yellow sparry calcite that records meteoric water invasion of the host mudrocks. An abundance of fatty acids in these spars indicates aqueous transport of organic breakdown products, and δ13C data suggest a predominantly methanogenic bicarbonate source. However, the wide δ18O range for petrographically identical cement (?1·3‰ to ?15·6‰) is difficult to explain. 相似文献