Geochemical,and stable and radiogenic isotope records in Devonian and Early Carboniferous carbonates from Valle de Tena,central Pyrenees (Spain): evidence for their diagenetic environments

Mineralogical, textural and geochemical investigations were made to determine the post-depositional evolution of Devonian and Early Carboniferous carbonates from Valle de Tena. The carbonate association is made up of low-Mg calcite, which occurs as micrite, spar cements, neomorphic patches and spar filling veinlets. Non-stoichiometric dolomite and ankerite occur as cements (dolomite also as replacements) in the Middle Devonian, post-dating calcite types. All these phases pre-date tectonic stylolites, indicating compaction after stabilization of the carbonate minerals. Strontium concentrations indicate that Early Devonian and Early Carboniferous micrites initially precipitated as aragonite; Middle and Late Devonian micrites precipitated as high-Mg calcites. Both precursors were diagenetically stabilized to low-Mg calcites through interaction with meteoric waters in phreatic environments. Trace elements in dolomite and ankerite indicate precipitation from Sr-enriched meteoric water. All studied carbonates, except Middle Devonian limestones, precipitated in reducing environments, which favoured incorporation of Fe and Mn. Late calcite generations precipitated from more saline waters than micrites. Light ¹⁸O values in micrites suggest alteration mainly in meteoric-phreatic environments. The dolomites and ankerites precipitated from more ¹⁸O-depleted fluids than the calcites, suggesting a greater contribution from meteoric waters. Variations in ¹³C of micrites represent primary secular trends, according to published ¹³C variations. The ¹³C oscillations within each succession probably relate to sea-level oscillations. Strontium isotopes also point to a meteoric origin of diagenetic fluids. Model calculations suggest that O and Sr isotopes equilibrated between calcites and fluid at relatively low water/rock ratios, whereas C isotopic signatures are inherited from limestones.     

Origin,characteristics and distribution of fault‐related and fracture‐related dolomitization: Insights from Mississippian carbonates,Isle of Man

Viséan limestones on the Isle of Man host numerous examples of fault‐controlled and fracture‐controlled dolomitization, which have been investigated to determine their macro‐scale to micro‐scale characteristics, geofluid origin, timing and relation to basin evolution. Geobodies composed of fabric destructive, ferroan, non‐planar dolomite range from several centimetres to >300 m wide and tens to hundreds of metres long parallel to faults and/or fractures; they have sharply defined margins, cross‐cut stratigraphy and locally finger out along beds or bed boundaries for tens of metres. Larger geobodies accompany NNE–SSW extensional faults with substantial breccia zones. One of these bodies hosts a sphalerite‐rich breccia deposit cemented by dolomite. Saddle dolomite lines or fills vugs and fractures within dolomite geobodies, and is a minor late diagenetic phase in undolomitized limestones. Replacive dolomite has low matrix porosity owing to non‐planar texture and associated cementation, and there is no evidence for subsequent leaching. Three dolomite stages are discriminated by texture, cathodoluminescence petrography and electron microscopy. Disseminated ‘Dolomite 1’ is substantially replaced and may be residual early diagenetic dolomite. Pervasive ‘Dolomite 2’ and ‘Dolomite 3’ have overlapping carbon–oxygen–strontium isotopic and fluid‐inclusion characteristics that indicate precipitation from allochthonous, high‐temperature (98 to 223°C) and high‐salinity (15 to 24 wt% NaCl eq.) brines. These variably equilibrated with host limestones and mixed with resident pore fluids. Overlying mudrocks formed a seal for ascending fluids. Integration of data from the mineral deposit suggests that fault‐fracture systems tapped different deep‐seated fluid reservoirs at different temperatures, and implies fluid interactions with both metamorphic basement and sedimentary cover in large‐scale circulation systems. This phenomenon probably took place during Mesozoic rifting, although an earlier event at the end of the Early Carboniferous cannot be discounted. In either case, a transient heat flow anomaly, previously unrecognized in the Irish Sea region, may be required to account for the hottest fluids.     

Reflux stratabound dolostone and hydrothermal volcanism-associated dolostone: a two-stage dolomitization model (Jurassic, Lebanon)

The Kesrouane Formation, which is characterized by pervasive dolomitization, has a stratigraphic thickness that exceeds 1000 m. It is part of a broad carbonate platform deposited in the Levant region and represents 60% of the Lebanese Jurassic rocks. Two genetically distinct dolostones are recognized within this unit: (1) fine‐to‐medium crystalline non‐planar grey dolostone; and (2) coarse‐crystalline planar beige dolostone. The former is stratabound and of Early Jurassic age (⁸⁷Sr/⁸⁶Sr = 0·707455). This dolostone locally exhi‐bits pseudomorphs of evaporite nodules, pointing towards seepage‐reflux dolomitization by hypersaline‐ to marine‐related fluids. Exposures of the coarse‐crystalline dolostone are associated with regional pre‐Cretaceous faults, along which Late Jurassic volcanics also occur. Sedimentological and diagenetic considerations coupled with microthermometry support a hydrothermal origin for this dolostone, with T_H values of primary inclusions between 50 and 80 °C. The related dolomitizing fluids are mesosaline (3·5–12·0 eq. wt% NaCl), and are believed to result from the mixing of evaporative brines and sea water. Dolomitization is thus believed to have occurred in two stages, whereby fluids invaded the host rocks first by seepage‐reflux, explaining the resulting Early Jurassic stratabound dolostone, and later through fracture flow along the faults associated with the Late Jurassic volcanism, explaining the coarse‐crystalline hydrothemal dolostone.     

The geochemistry of carbonate diagenesis: The past,present and future

Stable carbon and oxygen isotopes (δ¹⁸O and δ¹³C values) and trace elements have been applied to the study of diagenesis of carbonate rocks for over 50 years. As valuable as these insights have been, many problems regarding the interpretation of geochemical signals within mature rocks remain. For example, while the δ¹⁸O values of carbonate rocks are dependent both upon the temperature and the δ¹⁸O value of the fluid, and additional information including trace element composition aids in interpreting such signals, direct evidence of either the temperature or the composition of the fluids is required. Such information can be obtained by analysing the δ¹⁸O value of any fluid inclusions or by measuring the temperature using a method such as the ‘clumped’ isotope technique. Such data speak directly to a large number of problems in interpreting the oxygen isotope record including the well‐known tendency for δ¹⁸O values of carbonate rocks to decrease with increasing age. Unlike the δ¹⁸O, δ¹³C values of carbonates are considered to be less influenced by diagenesis and more a reflection of primary changes in the global carbon cycle through time. However, many studies have not sufficiently emphasized the effects of diagenesis and other post‐depositional influences on the eventual carbon isotopic composition of the rock with the classic paradigm that the present is the key to the past being frequently ignored. Finally, many additional proxies are poised to contribute to the interpretation of carbonate diagenesis. Although the study of carbonate diagenesis is at an exciting point with an explosion of new proxies and methods, care should be taken to understand both old and new proxies before applying them to the ancient record.     

华北蓟县中元古界剖面中燧石条带的形成机制——硼硅同位素证据

天津蓟县中新元古界海相沉积碳酸盐岩建造中分布大量燧石条带,特别是雾迷山组燧石条带与白云岩互层密集产出,沉积韵律非常明显,记录了其形成时海洋的化学和生物等信息,但关于其成因和形成机制还存在不同的认识。我们对蓟县中元古界剖面中碳酸盐岩的硼同位素和燧石条带的硅氧同位素进行了系统研究。燧石条带的 δ 30 Si NBS 28 值为0. 6‰~3. 3‰,平均2. 2‰,较热水化学沉积硅质岩的 δ 30 Si NBS 28 值显著偏高,与浅海生物沉积硅质岩的硅同位素组成相近。燧石条带的 δ 18 O V SMOW 值为21. 7‰~27. 8‰,平均25. 5‰,较热液成因硅质岩的值明显偏高,而与常温海相硅质岩的 δ 18 O值相似。蓟县剖面白云岩和灰岩等碳酸盐岩的 δ 11 B SRM 951 值为0‰~11. 0‰之间,平均4. 8‰,较现代海相碳酸盐的值明显偏低。高于庄组至雾迷山组燧石条带白云岩的 δ 11 B值普遍高于白云岩和灰岩的值,在3. 3‰~12. 9‰之间,平均8. 4‰。在酸性条件下富集重硼同位素的B(OH) 3掺入碳酸盐的比例增加,可导致其 δ 11 B值升高。这表明燧石条带白云岩可能形成于局部酸性水环境。结合碳酸盐和SiO 2溶解/沉淀与pH之间相互关系,提出蓟县剖面中的燧石条带是一种具有时代特征的同沉积的生物化学沉积硅质岩。中元古代海水中SiO 2浓度高,基本呈饱和状态,Mg/Ca比值高,生物活动已成为影响海洋环境的重要因素。在生物活动繁盛期大量有机质沉积于海底,导致海水-沉积物界面附近pH值大幅下降(pH＜7. 8),白云石等碳酸盐溶解度升高,难以沉淀;与此相反,SiO 2溶解度降低,达到过饱和,大量沉淀形成燧石条带/透镜体。生物活动羸弱期,海底pH值升高恢复到正常水平,SiO 2溶解度升高,碳酸盐溶解度降低,形成白云岩等碳酸盐沉淀。生物活动的周期性变化,则形成白云岩与燧石互层的条带状韵律层。燧石条带白云岩的硼同位素组成反映的是局部流体的 δ 11 B和pH值,不适合用来反演海水的硼同位素组成。     

Diagenetic formation of gypsum and dolomite in a cold‐water coral mound in the Porcupine Seabight,off Ireland

Authigenic gypsum was found in a gravity core, retrieved from the top of Mound Perseverance, a giant cold‐water coral mound in the Porcupine Basin, off Ireland. The occurrence of gypsum in such an environment is intriguing, because gypsum, a classic evaporitic mineral, is undersaturated with respect to sea water. Sedimentological, petrographic and isotopic evidence point to diagenetic formation of the gypsum, tied to oxidation of sedimentary sulphide minerals (i.e. pyrite). This oxidation is attributed to a phase of increased bottom currents which caused erosion and enhanced inflow of oxidizing fluids into the mound sediments. The oxidation of pyrite produced acidity, causing carbonate dissolution and subsequently leading to pore‐water oversaturation with respect to gypsum and dolomite. Calculations based on the isotopic compositions of gypsum and pyrite reveal that between 21·6% and 28·6% of the sulphate incorporated into the gypsum derived from pyrite oxidation. The dissolution of carbonate increased the porosity in the affected sediment layer but promoted lithification of the sediments at the sediment‐water interface. Thus, authigenic gypsum can serve as a signature for diagenetic oxidation events in carbonate‐rich sediments. These observations demonstrate that fluid flow, steered by environmental factors, has an important effect on the diagenesis of coral mounds.     

白云鄂博Fe-REE-Nb建造地球化学特征及成因：元素及同位素新证据

通过野外地质观察和室内镜下研究,利用XRF和ICP-MS对白云岩及其周围的板岩的主、微量元素进行分析,同时对硫化矿化的样品开展硫同位素测试。元素测试结果显示白云鄂博Fe-REE-Nb建造白云岩既具有部分火成碳酸岩的地球化学特征,也具有部分沉积碳酸岩的地球化学特征,表明白云鄂博Fe-REE-Nb建造赋矿白云岩不是典型的火成碳酸岩或沉积碳酸盐岩。硫同位素的测试结果表明,全岩的硫同位素组成不呈塔式模型分布,出现两个比较明显的峰值,一个在0‰左右,具有深源特征;另一个在+8‰左右,明显高于幔源硫,这个结果说明其来源可能有两个:地幔和海水。赋矿白云岩中Nb随着稀土的富集也发生富集作用,但是Ta的富集作用却十分微弱,显示了成矿热液强烈富REE和Nb及贫Ta的元素地球化学特征。据元素和硫同位素结果,我们认为白云鄂博赋矿白云岩是沉积碳酸盐受地幔碳酸岩岩浆及派生的流体交代的产物,而非直接源于火山碳酸岩喷发成因。地幔深部碳酸岩岩浆及其派生的富稀土流体沿区域性深大断裂上涌与沉积碳酸盐岩进行交代作用,形成了白云鄂博独特巨大的Fe-REE-Nb矿床及区域性的稀土矿床。     

Stable and clumped isotopes in desert carbonate spring and lake deposits reveal palaeohydrology: A case study of the Lower Jurassic Navajo Sandstone,south‐western USA

Carbon, oxygen and clumped isotope (Δ₄₇) values were measured from lacustrine and tufa (spring)‐mound carbonate deposits in the Lower Jurassic Navajo Sandstone of southern Utah and northern Arizona in order to understand the palaeohydrology. These carbonate deposits are enriched in both ¹⁸O and ¹³C across the basin from east to west; neither isotope is strongly sensitive to the carbonate facies. However, ¹⁸O is enriched in lake carbonate deposits compared to the associated spring mounds. This is consistent with evaporation of the spring waters as they exited the mounds and were retained in interdune lakes. Clumped isotopes (Δ₄₇) exhibit minor systematic differences between lake and tufa‐mound temperatures, suggesting that the rate of carbonate formation under ambient conditions was moderate. These clumped isotope values imply palaeotemperature elevated beyond reasonable surface temperatures (54 to 86°C), which indicates limited bond reordering at estimated burial depths of ca 4 to 5 km, consistent with independent estimates of sediment thickness and burial depth gradients across the basin. Although clumped isotopes do not provide surface temperature information in this case, they still provide useful burial information and support interpretations of the evolution of groundwater locally. The findings of this study significantly extend the utility of combining stable isotope and clumped isotope methods into aeolian environments.     

Lead contamination in a wetland watershed: isotopes as fingerprints of pollution

The Pb-isotope composition of soils and sediments has been measured from both highly contaminated and non-contaminated regions of Bayou Trepagnier, a bayou in southern Louisiana that has had oil refinery effluent discharged into it over the past 66 years. Spoil banks created by the dredging of the bayou bottom approximately 50 years ago are the main source of contamination within the ecosystem. The ²⁰⁶Pb/²⁰⁷Pb isotope composition of the contaminant is relatively constant averaging 1.275 ±0.008. A literature search reveals that such radiogenic values are typical of ores from southeastern Missouri. When surficial soil ²⁰⁶Pb/²⁰⁸Pb and ²⁰⁶Pb/²⁰⁷Pb isotope ratios are plotted against each other, a straight line is defined (r²=0.99). The linear correlation suggests mixing between Pb from the spoil banks and Pb from a natural source. The latter source may consist of Pb in soil that has been leached of its natural radiogenic component during weathering processes. Mixing calculations indicate that transport of contaminant Pb is widespread and occurs several hundred meters from the spoil banks. Despite the low Pb concentrations of some of the soils, the isotope data demonstrate that a significant amount of the Pb is derived from the pollutant source. Received: 12 July 1999 · Accepted: 14 September 1999     

Oxygen and carbon isotope composition of Gordon Group carbonates (Ordovician), Florentine Valley,Tasmania, Australia

The Gordon Group carbonates consist of biota of the Chlorozoan assemblage, diverse non‐skeletal grains and abundant micrite and dolomite, similar to those of modern warm water carbonates. Cathodoluminescence studies indicate marine, meteoric and some burial cements. Dolomites replacing burrows, mudcracks and micrite formed during early diagenesis.

δ¹⁸O values (‐5 to ‐7%ō PDB) of the non‐luminescent fauna and marine cement are lighter than those of modern counterparts but are similar to those existing within low latitudes during the Ordovician because of the light δ¹⁸O values of Ordovician seawater (‐3 to ‐5%o SMOW). The δ¹⁸O difference (2%o) between marine and meteoric calcite indicates that Ordovician meteoric water was similar to that in modern subtropics. Values of δ¹³C relative to δ¹⁸O indicate that during the Early Ordovician there were higher atmospheric CO₂ levels than at present but during the Middle and Late Ordovician they became comparable with the present because of a change from ‘Greenhouse’ to glacial conditions. δ¹⁸O values of Late Ordovician seawater were heavier than in the Middle Ordovician mainly because of glaciation.

Dolomitization took place in marine to mixed‐marine waters while the original calcium carbonate was undergoing marine to meteoric diagenesis.     

Dolomite characteristics and diagenetic model of the Calcari Grigi Group (Asiago Plateau,Southern Alps – Italy): an example of multiphase dolomitization

A multidisciplinary study, conducted over the carbonate platform deposits of the Liassic Calcari Grigi Group (Southern Alps), highlighted how the use of outcrop analogues can contribute to better define the distribution of dolomitic bodies related to fault networks, to characterize the petrophysical properties of the dolomitic sequence and unravel a complex diagenetic history. This study was carried out in the Asiago Plateau (southernmost part of the eastern Southern Alps, northern Italy) which provides excellent outcrops of the Jurassic Calcari Grigi Group. The dolomitization of the Jurassic sequence is variable in terms of stratigraphic extension and geographic distribution. In the studied localities the dolomitization is generally limited to the Mount Zugna Formation and is characterized by an undulatory front, with ‘sub‐vertical dolomitic chimneys’ along the major faults. Within this unit, and often associated with faults, stacked high‐porosity and permeability bed‐parallel dolomitic bodies are developed that show excellent petrophysical properties. The dolomitic intervals are characterized by pervasive unimodal and patchy polymodal dolomite crystals. Thin section, cathodoluminescence, isotopic and fluid inclusion analyses were used to constrain the paragenetic evolution of the sequence which is similar in all the studied localities. The first dolomitization stage is marked by zoned dolomite crystals with a dull luminescent core. The porosity is thought to have increased after this stage, with dark blue luminescent dolomite accompanied by the corrosion of older crystals. The appearance of saddle dolomite marks the onset of the porosity reduction stage, ending with the infilling of vugs and the remaining open pores with calcite cement. The diagenetic evolution locally stopped at the saddle dolomite stage with the complete occlusion of the remaining pores. Paragenetic and fluid‐inclusion data suggest an evolutionary trend of increasing temperatures and decreasing salinity toward brackish fluids responsible for dolomite and calcite precipitation. The integration of the available data seem to indicate that the diagenetic evolution of the study area is related to: (i) the interplay between evolving fluids (from marine to brackish); (ii) the burial of the sequence (increasing temperature); and (iii) the evolution of the hydrogeological system (fault and fracture network, fluid mixing). This complex paragenetic evolution is strongly linked to the evolution of the porosity framework that evolved from a good, widespread network in the early stages of the burial history to a confined system in the later stages due to reduction of porosity by the deposition of late calcite and dolomite cements.     

Multiphase partial and selective dolomitization of Carnian reef limestone (Transdanubian Range,Hungary)

Partially dolomitized carbonate successions provide a good opportunity to understand the commonly multistage process of dolomitization. Petrographic methods, fluid inclusion microthermometry and stable isotope measurements were applied to reconstruct the diagenetic evolution and dolomitization of a partially dolomitized Carnian reef limestone from the Transdanubian Range, Hungary. The diagenetic history began with reef diagenesis and formation of dolomite micro‐aggregates in microbial fabric elements; this was followed by the development of euhedral porphyrotopic dolomite crystals through overgrowths around the previously formed dolomite micro‐aggregates during the earliest burial stage. Increasing burial resulted in the extension of the dolomite patches via formation of finely crystalline replacement dolomite. From the Late Norian, when the Carnian reef carbonates reached the depth of 1·0 to 1·8 km, the diagenetic evolution continued in an intermediate to deep‐burial setting. Contemporaneously, an extensional regime was established, leading to fracturing. The progressive burial resulted in the recrystallization of the pre‐existing dolomite with increasing temperature, while saddle dolomite cement was precipitated in fractures. In connection with the Alpine Orogeny, intense denudation took place during the Late Cretaceous, accompanied by fracturing. Similar tectonically controlled denudation and fracturing occurred in several stages during the Cenozoic. As a result of these processes, the studied Carnian carbonates were raised to a near‐surface position or became subaerially exposed, leading to dedolomitization of the last dolomite phase and precipitation of calcite cement in cavities and fractures. This study revealed that by investigating partially and selectively dolomitized rock types, it is possible to document and understand those stages of the multiple dolomitization process which can barely be detected in the completely dolomitized rock bodies. Recognition of the dolomitization phases could provide the basis for the analysis of their relations with the depositional, diagenetic and tectonic processes, and stages of basin evolution.     

Secular variations in seawater chemistry controlling dolomitization in shallow reflux systems: insights from reactive transport modelling

Dolomitization often plays a critical role in the pore network development of platform carbonates, with implications for reservoir quality distribution. Understanding both the hydrological system driving dolomitization and the chemistry of the fluids involved is fundamental to constrain predictions of the geometry and the petrophysical properties of dolomite bodies. Here, the role of secular variations in seawater Mg/Ca as a control on dolomitization and early porosity modification was evaluated using one‐dimensional reactive transport models and fluids based on modern (aragonite sea), Mississippian and Aptian (calcite sea) seawaters. The sensitivity of dolomitization to a range of extrinsic controls (brine salinity, temperature, fluid flow rate and pCO₂) and to intrinsic reactivity of the sediments (effective reactive surface area) was also explored. Simulations suggest faster calcite replacement by dolomite for seawaters with higher Mg/Ca, indicating that dolomitization potential is determined more by Mg/Ca rather than saturation index. Increasing evaporative concentration enhances reaction rate independent of the effect of enhanced density‐driven fluid flux. In addition to brine composition, effective surface area of precursor sediments and temperature exert a critical control on replacement rate, while secular variations of pH and carbonate alkalinity associated with changes in pCO₂ are only secondary controls. Above flow rates of 0·01 m yr^?1 replacive dolomitization is reaction‐limited rather than flux limited, favouring alteration of fine‐grained carbonates and suggesting that preferential alteration of grainstone units is rare unless head gradients are low. Post‐replacement dolomite cementation is flux dependent, and thus favoured in areas of high head gradient and high permeability sediments and, contrary to replacement, supersaturation is a more important driver than Mg/Ca. While uncertainties remain regarding low‐temperature dolomitization kinetics, the capability of numerical simulations to decouple individual controls provides new insights which can be used, in conjunction with traditional comparative sedimentology, to generate more rigorous conceptual models for individual reservoir settings.     

重大地质转折期的碳、硫循环与环境演变

碳、硫在表层储库和地质储库以不同的形式相互转换,在这个过程中都伴随着一定的同位素分馏。碳同位素的分馏主要受到光合作用以及海水溶解无机碳与大气CO2交换的控制,而硫同位素的分馏则主要受控于硫酸盐细菌还原作用。表层储库碳、硫同位素的组成通过地质作用被很好地保存在地质储库中,因此通过对地质储库中碳、硫同位素的分析和研究,可以很好地了解地球各圈层相互作用的规律,重塑地质历史特别是重大关键转折时期的演化过程。同时文中借助一些碳、硫同位素应用实例,进一步加深理解影响碳、硫同位素组成和变化的原因,以提高对不同时期全球环境变化的认知程度。     

华北地幔捕虏体Fe-Mg-Ca同位素研究进展

近年来,得益于同位素分析技术和质谱仪器性能的提高,使得铁（Fe）、镁（Mg）和钙（Ca）等非传统稳定同位素的高精度测量成为可能,并很快在地球化学、天体化学和生物地球化学等研究领域取得了丰硕的成果。本文通过对比分析来自华北克拉通不同地区不同类型地幔捕虏体的Fe、Mg和Ca位素组成特征,揭示华北克拉通岩石圈地幔Fe、Mg和Ca同位素组成不均一性的成因,并在此基础上,探讨华北大陆岩石圈地幔演化过程如部分熔融、橄榄岩-熔体反应过程、熔体的性质和来源等科学问题,为华北克拉通岩石圈的演化过程提供新证据。

     

塔里木盆地北部下奥陶统碳酸盐岩孔洞充填物特征及其成岩环境分析

为了正确分析和评价碳酸盐岩溶蚀孔洞在埋藏成岩环境中的发育和保存条件,对塔里木盆地北部露头剖面中下奥陶统白云岩及其溶蚀孔洞的充填物进行了详细的矿物学和地球化学研究,试图对这类孔洞充填物沉淀时的成岩环境进行恢复。大型洞穴充填物的矿物学特征和微孔洞充填物扫描电镜的分析表明,此类孔洞的环带状充填物具有明显的世代性,由基岩向孔洞中心,至少可识别出4期充填物,即第1期的乳白色白云石,第2期的铁质浸染的杂色高镁方解石,第3期的无色透明白云石和第4期的自形石英。碳、氧同位素分析结果表明,孔洞充填物形成于高温条件,结合微量元素、稀土元素所示的成岩信息可进一步推断其形成于高温埋藏环境,而非现代表生暴露期的充填物;第1期和第3期白云石充填物形成在相对还原且高盐度的流体性质条件下,而第2期高镁方解石充填物沉淀时相对偏氧化,盐度也偏低。据下奥陶统此类4期充填物的特征分析可知,第2期高镁方解石充填物的发育可能与构造抬升导致成岩环境的改变有关。     

Types and Origin of Dolostones in Tarim Basin, Northwest China:Petrographic and Geochemical Evidence

In the Tarim Basin of northwestern China hydrocarbon deposits have been discovered in parts of the thick strata of Cambrian dolostones. Based on petrographic study, six types of dolostone have been distinguished: Type-1, pink mud-bearing silty crystalline dolostone (PMSD); Type-2, gypsum- and salt-bearing fine crystalline dolostone (GSFD); Type-3, fine crystalline dolostone with dolomite crystals with cloudy core and clear rim (CCFD); Type-4, deep gray mud-bearing silty crystalline dolostone (GMSD); Type-5, euhedral coarse crystalline dolostone (ECD); and Type-6, xenotopic coarse crystalline dolostone (XCD). Applying petrographic and geochemical methods, the genesis of the dolostones is studied in this paper. Normally, Type-1 dolostone shows U- and Mo-depleted characteristics, reflecting a more oxidized formation environment; High δ18O and the purple color are consistent with formation of Sabkha dolostones on a supratidal flat. Types 2, 3, 4 dolostones show strata formation, similar REE patterns and 87Sr/86Sr ratios with contemporaneous limestones, suggesting a penecontemporaneous origin from seawater. Types 5 and 6 dolostones commonly occur as interbedded rocks, indicating secondary genesis after diagenesis. Type-6 dolostone has the highest order degree (OD) values (average 0.86), the lowest oxygen isotope values and positive Eu anomalies, which are consistent with previously reported hydrothermal dolostones. Differently, Type-5 shows euhedral texture, higher δ18O value, similar REE characteristic and 87Sr/86Sr ratios in comparison with contemporaneous limestones, suggesting that this type might have been dolomitized by down-transferring evaporated seawater during shallow burial stage. Dolostone fluid sources, formation environments and crystallizing dynamics are summarized and possible genetic models for the six types are proposed.     

Lithofacies associations and stable isotopes of palustrine and calcrete carbonates: examples from an Indian Maastrichtian regolith

Detailed information on semi‐arid, palustrine carbonate–calcrete lithofacies associations in a sheetwash‐dominated regolith setting is sparse. This is addressed by studying the Lower Limestone of the Lameta Beds, a well‐exposed Maastrichtian regolith in central India. The general vertical lithofacies assemblage for this unit comprises: (a) basal calcareous siltstones and marls with charophytes, ostracods and gastropods; (b) buff micritic limestones associated in their upper parts with calcretized fissure‐fill sandstones; (c) sheetwash as fissure‐fill diamictites and thin pebbly sheets, locally developed over a few metres; and (d) sandy, nodular, brecciated and pisolitic calcretes at the top. The sequence is ‘regressive’, with upsection filling of topographic lows by increased sheetwash. Lateral lithofacies change is marked, but there are no permanent open‐water lake deposits. In topographic lows close to the water table, marshy palustrine or groundwater calcretes formed, whereas on better drained highs, brecciation and calcretization occurred. Prolonged exposure is implied, suggesting that shrinkage was the main cause of brecciation. Evidence for rhizobrecciation and other biological calcrete fabrics is sparse, contrasting with the emphasis on root‐related brecciation in many studies of palustrine lithofacies. Stable isotope (δ¹⁸O and δ¹³C) values are consistent with the palustrine limestones being fed from meteoric‐derived groundwater with a strong input of soil‐zone carbon. There is overlap of both δ¹⁸O and δ¹³C values from the various palustrine and calcrete fabrics co‐occurring at outcrop. This suggests that, in groundwater‐supported wetlands, conversion from palustrine carbonate to calcrete need not show isotopic expression, as the groundwater source and input of soil‐zone carbon are essentially unchanged. Cretaceous–Tertiary δ¹⁸O and δ¹³C values from palustrine lithofacies and associated calcretes appear to be strongly influenced by the inherited values from lakes and wetlands. Hydrologically closed lakes and marine‐influenced water bodies tend to result in low negative palustrine δ¹⁸O and δ¹³C values. During brecciation and calcretization, the degree of isotopic inheritance depends on whether or not alteration occurs in waters that are different from those of the original water body or wetland. Marked biological activity (e.g. rhizobrecciation or root mat development) during calcretization may lower δ¹³C values where C₃ plants are abundant but, in shrinkage‐dominated systems, δ¹³C values will be largely inherited from the palustrine limestones.     

Zebra dolomitization as a result of focused fluid flow in the Rocky Mountains Fold and Thrust Belt, Canada

Discordant zebra dolomite bodies occur locally in the Middle Cambrian Cathedral and Eldon Formations of the Main Ranges of the Canadian Rocky Mountains Fold and Thrust Belt. They are characterized by alternating dark grey (a) and white (b) bands, forming an ‘abba’ diagenetic cyclicity. These bands developed parallel to both bedding and cleavage. Dark grey (a) bands consist of fine (< 300 μm) non-planar crystalline impure dolomite. The white (b) bands are composed of coarse (up to several millimetres) milky-white pure saddle dolomites (b1) which are often covered by pore-lining zoned dolomite (b2). The b phases often possess a saddle-shaped morphology. In contrast to the replacement origin of the a dolomite, the zoned b2 dolomite rims are interpreted as a cement formed in open cavities. The b1 dolomite is interpreted as the result of recrystallization with diagenetic leaching of non-carbonate components. All the zebra dolomites studied are (nearly) stoichiometric and are characterized by enriched Na and depleted Sr concentrations. Fe and Mn concentrations in these dolomites differ depending on the sample locality. Fluid inclusion data indicate that the dolomites formed from relatively hot (T_H = 130–200 °C), saline (20–23 wt% CaCl₂ eq.) fluids. A diagenetic high temperature origin is also supported by depleted δ¹⁸O values (−20 to −14‰ VPDB). A contribution of ⁸⁷Sr-enriched fluids is reflected in the ⁸⁷Sr/⁸⁶Sr values (0·7091–0·7123). Zebra dolomite development is explained by focused fluid flow, which exploited areas of structural weaknesses (e.g. basin-platform, rim areas, faults, etc.). Expulsion of hot basinal brines in a tectonically active regime generated overpressures, which explains the development of secondary porosity during zebra dolomitization as well as the intra-zebra fracturing at decimetre to micrometre scale.     

Physical and chemical growth conditions of Ordovician organogenic deep-water dolomite concretions: implications for the δ18O of Early Palaeozoic sea water

The estimated depth of formation of authigenic dolomite concretions in the Middle Ordovician Cloridorme Formation, Quebec, ranges from < 1 m to 150–200 m below sea floor (mbsf) (mostly between < 1 and 25 mbsf), based on centre‐to‐margin variations in minus‐cement porosity (80–90% to 45–75%). Formation depths are > 350 mbsf (25–17% porosity) in the Lower Ordovician Levis Formation. Outward‐decreasing δ¹³C_VPDB values (10·2–0·8‰) suggest precipitation in the methane generation zone with an increasing contribution of light carbonate derived by advection from thermocatalytic reactions at depth. Anomalously low δ¹⁸O_VPDB values (centre‐to‐margin variations of ?0·4 to ?7·5‰) give reasonable temperatures for the concretion centres only if the δ¹⁸O of Ordovician sea water was negative (?6‰) and the bottom water was warm (> 15 °C). The 3–5‰ lower values for the concretion margins compared with the centres can be explained if, in addition, volcanic‐ash alteration, organic‐matter decomposition and/or advection of ¹⁸O‐depleted water lowered the δ¹⁸O of the pore water further by 2·0–4·0‰ during the first 25–200 m of burial. Reasonable growth temperatures for the margins of 17–20 °C are compatible with a lowering of the isotopic ratios by 1 to < 1·3‰ as a temperature effect. The systematic concentric isotope zonation of the concretions suggests that the well‐ordered near‐stoichiometric dolomite is a primary feature and not the result of recrystallization. Diagenetic dolomite beds of the Cloridorme Formation appear to have formed by coalescence of concretions, as shown by randomly sampled traverses that indicate formation at different subsurface depths. Growth of the Cloridorme dolomites was probably limited by calcium availability, at least 50% of which was derived from connate water, and the remainder by diffusion from sea water. Dolomite precipitation was favoured over calcite by very high sedimentation rates, the abundance of marine organic matter in the host sediment and a correspondingly thin sulphate reduction zone. Deep‐seated concretion growth in the Levis Formation required either internal sources for the participating ions (carbonate dissolution event) or porewater advection along faults.