Replacement of evaporites within the Permian Park City Formation, Bighorn Basin, Wyoming, USA

The Permian Park City Formation consists of cyclically bedded subtidal to supratidal carbonates, cherts and siltstones. Early diagenesis of Park City Formation carbonates occurred under the influence of waters ranging from evaporative brines to dilute meteoric solutions and resulted in evaporite emplacement (syndepositional nodules and cements), as well as dolomitization, silicification and leaching of carbonate grains. Major differences are seen, however, in the diagenetic patterns of subsurface and surface sections of Park City Formation rocks. Subsurface samples are characterized by extensively preserved evaporite crystals and nodules, and preserve evidence of significant silicification (chert, chalcedony and megaquartz) and minor calcitization of evaporites. In outcrop sections, the evaporites are more poorly preserved, and have been replaced by silica and calcite and also leached. The resultant mouldic porosity is filled with widespread, very coarse, blocky calcite spar. These replacements appear to be multistage phenomena. Field and petrographic evidence indicates that silicification involved direct replacement of evaporites and occurred during the early stages of burial prior to hydrocarbon migration. Siliceous sponge spicules provided a major source of silica, and the fluids involved in replacement were probably a mixture of marine and meteoric waters. A second period of replacement and minor calcitization is inferred to have occurred during deep burial (under the influence of thermochemical sulphate reduction), although the presence of hydrocarbons probably retarded most other diagenetic reactions during this time interval. The major period of evaporite diagenesis, however, occurred during late stage uplift. The late stage replacement and pore-filling calcites have δ¹³C values ranging from 0·5 to -25·3%, and δ¹⁸O values of -16·1 to -24·3₀ (PDB), reflecting extensive modification by meteoric water. Vigorous groundwater flow, associated with mid-Tertiary block faulting, led to migration of meteoric fluids through the porous carbonates to depths of several kilometres. These waters reacted with the in situ hydrocarbon-rich pore fluids and evaporite minerals, and precipitated calcite cements. The Tosi Chert appears to have been an even more open system to fluid migration during its burial and has undergone a much more complex diagenetic history, as evidenced by multiple episodes of silicification, calcitization (ferroan and non-ferroan), and hydrocarbon emplacement. The multistage replacement processes described here do not appear to be restricted to the Permian of Wyoming. Similarly complex patterns of alteration have been noted in the Permian of west Texas, New Mexico, Greenland and other areas, as well as in strata of other ages. Thus, multistage evaporite dissolution and replacement may well be the norm rather than the exception in the geological record.     

Burial-dominated cementation in non-tropical carbonates of the Oligocene Te Kuiti Group, New Zealand

Cementation of bryozoan-echinoid-benthic foraminiferal temperate shelf carbonates of the Oligocene Te Kuiti Group, North Island, New Zealand, occurred mainly during subsurface burial. The calcite cements in the limestones are dominated by equant and syntaxial rim spar which typically becomes ferroan (given an iron supply) and, compared to the skeletal material with normal marine δ¹⁸O values from +2 to −1‰, more depleted in ¹⁸O with depth of burial, the δ¹⁸O composition of bulk cement samples ranging from −1 to −7‰. These trends reflect the establishment in pore waters during sediment burial of reducing conditions and gradually increasing temperatures (20–50°C), respectively. The δ¹³C values (0 to +3‰) of the cements remain the same as the host marine shells, suggesting the source of carbon in the cements was simply redistributed marine carbonate derived from shell dissolution.

Two gradational burial diagenetic environments influenced by marine-derived porewaters are arbitrarily distinguished: shallow burial phase and moderate burial phase. During the shallow burial phase, down to 500–600 m sub-bottom depth, the carbonates lost at least 25% of their original porosity by mechanical compaction and were selectively cemented by non-ferroan or usually ferroan, variably luminescent, slightly ¹⁸O-depleted sparry calcite cement (δ¹⁸O −2 to −4‰), mainly as syntaxial rims about echinoid grains. These shallow-burial cements form less than about 10% of total cement in the majority of the limestones and their source was probably mainly mild intergranular dissolution of calcitic skeletal fragments accompanying the onset of chemical compaction. During the moderate burial phase, between about 600 and 1100 m sub-bottom depth, porosity loss continued (typically to about 70% of its original value) as a result of pressure-solution of calcitic bioclasts associated with more advanced stages of chemical compaction. This involved development of a wide variety of non-sutured and microstylolitic solution seams, including both single and composite, wispy or continuous, bedding-parallel types and non-parallel reticulate forms. The released carbonate was precipitated as ferroan (or non-ferroan where iron supply was negligible), dull luminescent, strongly ¹⁸O-depleted (δ¹⁸O −4 to −7‰), mainly equant calcite spar cement, occluding available pore space in the limestones.     

贵州紫云上石炭统叶状藻礁灰岩的成岩作用

贵州紫云县猴场镇扁平村的上石炭统中的叶状藻礁及其周边灰岩中发育强烈的成岩作用和胶结物,这些胶结物在猴场研究区内是显著的和有代表性的。通过观察、分析野外露头、光片、薄片、薄片的阴极发光和染色,来研究礁体岩石的成岩作用,确定了成岩作用序列、成岩环境、成岩阶段。成岩作用类型主要有泥晶化、溶蚀、胶结、新生变形、机械压实、剪切或...     

Depositional Environments and Diagenesis of the Kuldhar and Keera Dome Carbonates (Late Bathonian–Early Callovian) of Western India

This paper describes 11 microfacies types in late Bathonian–Early Callovian carbonates of the Kuldhar Member of the Jaisalmer Formation (Rajasthan) and the Keera Golden Oolite Member of the Chari Formation (Kachchh Mainland) western India. The different microfacies associations reported in this study reflect an ideal shallowing upward sequence, representing a system of bioclastic bars developed on the lower ramp, evolving into an oolitic bar-to-bank system separating restricted lagoonal—from lower ramp environment. Four main types of cements, i.e. bladed, fibrous, syntaxial overgrowth and blocky cement (characterized in a few cases by ferroan calcite and anhydrite II) occur in these carbonates. The study also reveals that chemical compaction followed the two phases of early mechanical compaction that largely governed porosity of these limestones. However, micritization and neomorphism also contributed significantly in this respect. Diagenetic signatures in these carbonates suggest that marine phreatic and fresh water phreatic environments dominated, but deep burial diagenesis also played its role in shaping these rocks. The early and late diagenetic changes have been controlled by the depositional facies evolving in a basin riddled with rifting in an extensional tectonic regime forcing regional-scale sea level fluctuations.     

Origin and diagenetic evolution of Ca–Mg–Fe carbonates in some coalfields of Japan

Carbonate concretions, lenses and bands in the Pleistocene, Palaeogene and Upper Triassic coalfields of Japan consist of various carbonate minerals with varied chemical compositions. Authigenic carbonates in freshwater sediments are siderite > calcite > ankerite > dolomite >> ferroan magnesite; in brackish water to marine sediments in the coal measures, calcite > dolomite > ankerite > siderite >> ferroan magnesite; and in the overlying marine deposits, calcite > dolomite >> siderite. Most carbonates were formed progressively during burial within a range of depths between the sediment-water interface and approximately 3 km. The mineral species and the chemical composition of the carbonates are controlled primarily by the initial sedimentary facies of the host sediments and secondarily by the diagenetic evolution of pore water during burial. Based on the regular sequence and burial depth of precipitation of authigenic carbonates in a specific sedimentary facies, three diagenetic stages of carbonates are proposed. Carbonates formed during Stage I (< 500 m) strongly reflect the initial sedimentary facies, e.g. low Ca-Mg siderite in freshwater sediments which are initially rich in iron derived from lateritic soil on the nearby landmass, and Mg calcite and dolomite in brackish-marine sediments whose pore waters abound in Ca²⁺ and Mg²⁺ originating in seawater and calcareous shells. Carbonates formed during Stage II (500–2000 m) include high Ca-Mg siderite, ankerite, Fe dolomite and Fe–Mg calcite in freshwater sediments. The assemblage of Stage II carbonates in brackish-marine sediments in the coal measures is similar to that in freshwater sediments. This suggests similar diagenetic environments owing to an effective migration and mixing of pore water due to the compaction of host sediments. Carbonates formed during Stage III (> 2000 m) are Fe calcite and extremely high Ca-Mg siderite; the latter is exclusively in marine mudstones. The supply of Ca is partly from the alteration of silicates in the sediments at elevated burial temperatures. After uplift, calcite with low Mg content precipitates from percolating groundwater and fills extensional cracks.     

Diagenetic alterations of the upper Jurassic scleractinian corals,Hanifa Formation,Jabal Al-Abakkayn,central Saudi Arabia

During diagenetic stages, the aragonitic skeletons and the inter/intra-corallite cement of the upper Jurassic corals of Hanifa Formation either dissolved or subjected to diagenetic alterations including cementation, micritization, recrystallization, silicification, dolomitization and dedolomitization. The proposed sequence of diagenetic stages is as follows: early marine diagenesis, early meteoric and mixing zone diagenesis, late meteoric diagenesis, and shallow burial diagenesis. Each stage is characterized by certain diagenetic processes. The source of sulfate solutions for dedolomitization in the studied corals is the dissolved anhydrite deposits of the Arab–Hith Formations, sometime before their erosion. A possible source of silica, needed for the formation of chert and chalcedony, is the sponge spicules dispersed in many carbonates of the Hanifa Formation.     

Contrasting diagenesis of two Carboniferous Oolites from South Wales: a tale of climatic influence

Two oolites in the Dinantian (Mississippian/Lower Carboniferous) of Glamorgan, SW Britain, were deposited in similar depositional environments but have contrasting diagenetic histories. The Brofiscin and Gully Oolites occur in the upper parts of shallowing-upward sequences, formed through strandplain progradation and sand shoal and barrier growth upon a southward-dipping carbonate ramp. The Brofiscin Oolite is characterized by a first-generation cement of equant calcite spar, preferentially located at grain-contacts and forming non-isopachous fringes around grains, interpreted as meteoric vadose and phreatic in origin. Isopachous fibrous calcite fringes of marine origin are rather rare and occur only at a few horizons. Burial compaction was not important and porosity was occluded by poikilotopic calcite spar. Fitted grain-grain contacts locally occur and could be the result of near-surface vadose dissolution-compaction. Syntaxial overgrowths on echinoderm debris are common. Pre-compaction overgrowths are cloudy (inclusion-rich) and probably of meteoric origin, and post-compaction overgrowths are inclusion-free. By contrast, the Gully Oolite has little first-generation cement. However, marine fibrous calcite is common in oolitic intraclasts, as isopachous fringes of acicular calcite crystals closely associated with peloidal internal sediment; and early equant, drusy calcite spar occurs in the uppermost part of the Gully, beneath a prominent palaeokarst where pedogenic cements also occur. The major feature of Gully diagenesis is burial compaction, resulting in extensive grain-grain dissolution and microstylolitic grain contacts, and post-compaction poikilotopic spar occluded remaining porosity. The Brofiscin Oolite is pervasively dolomitized up-dip but the Gully Oolite for the most part only contains scattered pre-compaction dolomite rhombs and late veins of baroque dolomite, with less pervasive dolomitization. The difference in diagenetic style of the two Dinantian oolites is attributed to prevailing climate. The paucity of early meteoric cements in the Gully is a result of an arid climate, and this is supported by the nature of the capping palaeokarst. The abundant meteoric cements in the Brofiscin reflect a more humid climate, and effective meteoric recharge also resulted in up-dip pervasive mixing-zone dolomitization. The style of early diagenesis in these two oolites exerted a major control on the later burial diagenesis: in the Brofiscin, the early cements inhibited grain-grain dissolution and pressure solution, while these processes operated extensively in the Gully Oolite. Thus, prevailing climate can influence a limestone's diagenetic history from near-surface through into deep burial.     

Diagenesis of Barremian-Aptian platform carbonates (the Urgonian Limestone Formation of SE France): near-surface and shallow-burial diagenesis

The diagenesis of carbonate platform sediments is controlled by the original facies and mineralogy, climate, sea-level changes and burial history; these controls are clearly seen in the diagenesis of the Urgonian platform carbonates of SE France. Early diagenesis in the Urgonian platform included the precipitation of marine cements, dissolution of rudist shells and minor karstification. Diagenetic features produced during this phase were controlled by several falls in relative sea-level during the Barremian to mid-Aptian punctuating platform sedimentation, the original mineralogy of the sediment and the prevailing semi-arid/arid climate in the region at this time. Following a relative sea-level rise and further sedimentation, progressive burial of the platform led to minor compaction, followed by precipitation of coarse, equant, zoned to non-luminescent, calcite cement. This cement was cut by later stylolites, suggesting a relatively shallow-burial origin. Stable isotope (mean values - 7.94%δ¹⁸O and 0.36%δ¹³C) and trace element (mean values of Fe 334 ppm, Mn 92 ppm and Sr 213 ppm) data suggest that these cements precipitated from meteoric fluids at temperatures slightly elevated relative to depositional temperatures. A variable thickness of replacive dolomite which occurs preferentially within the shelf-margin facies of the lower part of the Urgonian post-dates mechanical fracturing and chemical compaction, but pre-dates the main phase of stylolitization. It is probable that the dolomitizing fluid was sourced by the early compaction-driven release of connate fluids held within the underlying muddy units. The burial history of these rocks suggests that calcite cementation and dolomitization took place at relatively shallow burial depths (1–1.5 km). The overall diagenetic history of the Urgonian Limestone Formation is a reflection of the pre-conditioning of the platform limestones by climate, sea level, tectonics and the shallow burial depths experienced by the platform during the later Mesozoic.     

Fluid–rock interactions associated with regional tectonics and basin evolution

An integrated approach consisting of fracture analysis, petrography, carbon, oxygen and strontium‐isotope analyses, as well as fluid‐inclusion micro‐thermometry, led to a better understanding of the evolution of fluid–rock interactions and diagenesis of the Upper Permian to Upper Triassic carbonates of the United Arab Emirates. The deposited carbonates were first marked by extensive early dolomitization. During progressive burial, the carbonates were affected by dolomite recrystallization as well as precipitation of vug and fracture‐filling dolomite, quartz and calcite cements. After considerable burial during the Middle Cretaceous, sub‐vertical north–south oriented fractures (F1) were cemented by dolomite derived from mesosaline to hypersaline fluids. Upon the Late Cretaceous maximum burial and ophiolite obduction, sub‐vertical east–west fractures (F2) were cemented by dolomite (Dc2) and saddle dolomite (Ds) derived from hot, highly saline fluids. Then, minor quartz cement has precipitated in fractures from hydrothermal brines. Fluid‐inclusion analyses of the various diagenetic phases imply the involvement of increasingly hot (200°C) saline brines (20 to 23% NaCl eq.). Through one‐dimensional burial history numerical modelling, the maximum temperatures reached by the studied rocks are estimated to be in the range of 160 to 200°C. Tectonically‐driven flux of hot fluids and associated diagenetic products are interpreted to have initiated during the Late Cretaceous maximum burial and lasted until the Oligocene–Miocene compressional tectonics and related uplift. The circulation of such hydrothermal brines led to partial dissolution of dolomites (Dc2 and Ds) and to precipitation of hydrothermal calcite C1 in new (mainly oriented north–south; F3) and pre‐existing, reactivated fractures. The integration of the obtained data confirms that the diagenetic evolution was controlled primarily by the interplay of the burial thermal evolution of the basin and the regional tectonic history. Hence, this contribution highlights the impacts of regional tectonics and basin history on diagenetic processes, which may subsequently affect reservoir properties.     

川东北下侏罗统大安寨段陆相页岩方解石成因

为分析陆相页岩中方解石的成因及其对储层的影响,以四川盆地下侏罗统大安寨段的介壳泥岩与灰岩夹层为主要研究对象,利用X-射线衍射、普通薄片、岩芯观察、阴极发光及电子探针测试手段,识别出文石转化方解石、胶结物方解石和重结晶作用形成的方解石.在同生期和成岩早期,生物介壳中的文石转化为泥晶无铁方解石,阴极发光为橙黄色.成岩早期,...     

Compaction in halite-cemented carbonates – the Dawson Bay Formation (Middle Devonian) of Saskatchewan, Canada

Halite-impregnated carbonates in the Dawson Bay Formation of Saskatchewan lie between beds of halite and are buried to a depth of 1 km. They exhibit two different diagenetic styles – some resisted compaction and had high pre-salt porosities; others contain compaction-broken fossils and pressure-solution seams. The uncompacted rocks, together with the difficulty of explaining how halite cement could enter the Dawson Bay after overlying bedded halites were deposited, suggest that halite cementation occurred early with only a few tens of metres of overburden. Early diagenetic compaction is suggested by the presence of unbroken, displacive skeletal halite crystals, which cross-cut compaction structures, and by the difficulty of explaining how (1) later compaction could occur in halite-cemented rocks and (2) how pore-fluids could be expelled after surrounding rocks lost their permeability. The organic-rich nature of many carbonates may explain why compaction was both early and extensive, but this explanation fails to explain how similar compaction developed in horizons with lower organic contents. Chemical compaction may also have been enhanced by aragonite dissolution during seawater evaporation or brine dilution. Early chemical compaction in Dawson Bay carbonates indicates that compaction in other carbonates need not signify deep burial diagenesis; neither can compaction be used indiscriminately to identify other diagenetic events as being of deep burial origin. Early halite cementation, as in the Dawson Bay Formation, preserves carbonates at early diagenetic stages and may thus preserve geochemical information unmodified by later diagenesis.     

Diagenesis and Fluid Flow History in Sandstones of the Upper Permian Black Jack Formation, Gunnedah Basin, Eastern Australia

The fluid flow history during diagenesis of sandstones in the Upper Permian Black Jack Formation of the Gunnedah Basin has been investigated through integrated petrographic observations, fluid inclusion investigations and stable isotope analyses. The early precipitation of mixed-layer illite/smectite, siderite, calcite, ankerite and kaolin proceeded at the presence of Late Permian connate meteoric waters at temperatures of up to 60℃. These evolved connate pore waters were also parental to quartz, which formed at temperatures of up to 87℃. The phase of maximum burial was characterized by development of filamentous illite and late calcite at temperatures of up to -90℃. Subsequent uplifting and cooling led to deep meteoric influx from surface, which in turn resulted in dissolution of labile grains and carbonate cements, and formation of second generation of kaolin. Dawsonite was the last diagenetic mineral precipitated and its formation is genetically related to deep-seated mamagtic sourced CO2.     

Calcite precipitation and Recrystallization fabrics—their significance in Jurassic Limestones of Europe

Many fabrics in Corallian (Upper Jurassic) carbonates in England, France and Switzerland are bigenetic, forming by solution/precipitation and recrystallization processes. Early precipitated cements are non‐ferroan, whereas those formed later are decidedly ferroan. Mossbauer spectroscopy has shown that the iron in the carbonates is largely divalent, substituting for calcium in the calcite lattice. The cements may be subdivided into those forming in an oxidizing environment, and those forming in a reducing environment. Fabric evidence indicates that a solution period separates the two cement phases. The diagenetic history is linked with the sedimentation pattern. Thus, under progressive build up of sediments into shallow‐water or supratidal conditions, the first‐phase cement probably precipitated from non‐marine, partially oxygenated vadose water. Subsequent subsidence and sedimentation resulted in the depression of partially cemented sediments into zones within the sedimentary pile conducive first to pyrite precipitation, and then to ferroan calcite precipitation. Fabrics can therefore be used to interpret the diagenetic environment of regressive sedimentary associations.     

Carbonate Diagenesis Controlled by Glacioeustatic Sea-Level Changes： A Case Study from the Carboniferous-Permian Boundary Section at Xikou, China

The diagenesis of modern and ancient carbonatesedi ments has been widely studied and systematicallyreviewed since the 1960s (e .g. Moore ,2001 ,1989 ;Wang et al ., 1994 , 1991 ; McIlreath and Morrow,1990 ; Tucker and Bathurst , 1990 ; Schneidermannand Harris , 1985 ; Longman, 1980 ; Bathurst ,1975) . With the development of sequence stratigra-phy and its more widespread application, discussionabout the relationship between diagenesis and se-quence stratigraphy/sea-level changes ,as well as…     

碳酸盐沉积物的成岩作用

化学沉淀碳酸盐矿物在沉积后很容易受到各种作用的影响,其中最重要的是其在成岩阶段所经历的成岩作用.碳酸盐沉积物在成岩过程中主要受大气降水、海水和埋藏过程中孔隙流体的控制,经历一系列压实、溶解、矿物的多相转变、重结晶、胶结等成岩作用,逐渐转变为固结的岩石.在成岩过程中,由于孔隙流体与沉积流体之间的异同以及温度的变化,碳酸盐沉积物的原始矿物成分、地球化学特征可能会很好的保存下来,但在许多情况下,也可能会改变,从而使我们无法准确反演碳酸盐沉积物在沉积时水体的特征.因此,我们在应用碳酸盐岩重建相关古环境和古气候变化的时候,必须要通过有效的方法来对碳酸盐岩是否受到成岩作用的影响进行鉴定.     

Diagenesis and reservoir quality analysis in the Lower Cretaceous Qishn sandstones from Masila oilfields in the Sayun–Masila Basin,eastern Yemen

Lower Cretaceous sandstones of the Qishn Formation have been studied by integrating sedimentological, petrological and petrophysical analyses from wells in the Masila oilfields of eastern Yemen. These analyses were used to define the origin, type of diagenesis and its relation to reservoir quality. The sandstones of the Qishn Formation are predominately quartz arenite to subarkose arenite with sublitharenite and quartz wackes displaying a range of porosities, averaging 22.33%. Permeability is likewise variable with an average of 2844.2 mD. Cementation coupled with compaction had an important effect on porosity destruction after sedimentation and burial. The widespread occurrence of early calcite cement suggests that the sandstones of the Qishn Formation lost significant primary porosity at an early stage of its diagenetic history. In addition to poikilotopic calcite, several different cements including kaolinite, illite, chlorite and minor illite–smectite occur as pore‐filling and pore‐lining cements, which were either accompanied by or followed the development of the early calcite cement. Secondary porosity development occurred due to partial to complete dissolution of early calcite cements and feldspar grains. The new data presented in this paper suggest the reservoir quality of Qishn sandstones is strongly linked to their diagenetic history; hence, the reservoir quality is reduced by clay minerals, calcite and silica cements but is enhanced by the dissolution of the unstable grains, in addition to partial or complete dissolution of calcite cements and unstable grains. Copyright © 2015 John Wiley & Sons, Ltd.     

黄骅坳陷三马地区中-深部储层成岩作用及主控因素分析

黄骅坳陷三马地区储集岩样品的显微特征及成岩矿物的组合关系分析结果表明，三马地区下第三系中深层储层主要处于晚成岩A期，成岩现象包括石英、长石的次生加大、碳酸盐矿物胶结作用、矿物交代作用、溶解作用和粘土矿物转化作用等。其中石英次生加大于2700m左右开始出现，随埋深增大，石英增生加强；长石次生加大现象不十分普遍；碳酸盐胶结作用包括早期自生泥晶方解石胶结作用、连晶方解石和晚期白云石(或铁方解石)的胶结作用。在扫描电镜下可见到方解石与含铁方解石集合体充填在粒间孔隙中或与石英、钠长石及粘土矿物共生，白云岩多呈菱形粒状分布于粒间；常见的交代现象主要有方解石交代长石、石英及粘土矿物，粘土矿物交代长石、石英等；溶解作用主要有长石的溶解、碳酸盐颗粒的溶解和方解石胶结物的溶解等，粘土矿物的转化主要为蒙脱石、高岭石向伊利石(或绿泥石)转化。还讨论了储层岩相、岩性特征、孔隙水中有机酸含量、早期方解石的充填、烃类早期注入等因素对储层成岩演化的控制作用。     

西沙群岛晚第四纪碳酸盐岩淡水成岩作用

基于西沙永兴岛上最新钻孔（SSZK1）取得的55.92 m岩芯的 U?Th定年、矿物、薄片、主微量元素及碳氧稳定同位素等资料,开展了西沙群岛晚第四纪碳酸盐岩沉积相和淡水成岩作用的研究。根据不同的矿物组成特征,可将SSZK1钻孔岩芯分为上、中、下三段: 下 段（33.89~55.92 m,主要为低镁方解石）、中 段（18.39~33.89 m,主要为文石和低镁方解石）、上段（0~18.39 m,主要为文石、高镁方解石和低镁方解石）。由于下段碳酸盐岩几乎全为稳定的低镁方解石组成,碳氧同位素值的严重负偏和小幅度变化,可推断其经历了程度较大的淡水成岩作用。中段和上段还存在不稳定的文石和高镁方解石,碳氧同位素值相对下段正偏和高幅高频变化,推测其淡水成岩作用的程度比下段要小。中段碳氧同位素值高幅高频变化同时也说明该段的矿物纵向变化较复杂。这种矿物组成的复杂变化可能是由于晚第四纪海平面频繁变化,该段被大气水渗流带和潜流带交替占据引起的。主微量元素的变化同时受到淡水成岩作用和沉积环境的影响。在中段、下段中可识别出sq1、sq2、sq3、sq4四个完整的相旋回。Na₂O,S,Sr 和碳氧同位素受到的淡水成岩作用而被消耗和负偏,且由于老一期的旋回经历了更长时间的淡水成岩作用,新、老旋回间的 Na₂O,S,Sr含量值和碳氧同位素值有明显差异。利用新、老时期形成的旋回间淡水成岩作用剩余Na₂O,S,Sr含量和碳氧同位素值的差别可以将新、老两个旋回区分开来。     

Calcite cementation during bacterial manganese, iron and sulphate reduction in Jurassic shallow marine carbonates

Faunally restricted argillaceous wackestones from the Middle Jurassic of eastern England contain evidence of early diagenetic skeletal aragonite dissolution and stabilization of the carbonate matrix, closely followed by precipitation of zoned calcite cements, and precipitation of pyrite. Distinctive cathodoluminescence and trace element trends through the authigenic calcites, their negative δ¹³C compositions and the location of pyrite in the paragenetic sequence indicate that calcite precipitation took place during sequential bacterial Mn, Fe and sulphate reduction. Calcite δ¹⁸O values are compatible with cementation from essentially marine pore fluids, although compositions vary owing to minor contamination with ¹⁸O-depleted ‘late’cements. Mg and Sr concentrations in the calcites are lower than those in recent marine calcite cements. This may be a result of kinetic factors associated with the shallow burial cementation microenvironments. Bicarbonate for sustained precipitation of the authigenic calcites was derived largely from aragonite remobilization, augmented by that produced through anaerobic organic matter oxidation in the metal and sulphate reduction environments. Aragonite dissolution is thought to have been induced by acidity generated during aerobic bacterial oxidation of organic matter. Distinction of post-oxic metal reduction and anoxic sulphate reduction diagenetic environments in modern carbonate sediments is uncommon outside pelagic settings, and early bacterially mediated diagenesis in modern platform carbonates is associated with extensive carbonate dissolution. High detrital Fe contents of the Jurassic sediments, and their restricted depositional environment, were probably the critical factors promoting early cementation. These precipitates constitute a unique example of calcite authigenesis in shallow water limestones during bacterial Mn and Fe reduction.     

Shallow-marine carbonate cementation in Holocene segments of the calcifying green alga Halimeda

Early-diagenetic cementation of tropical carbonates results from the combination of numerous physico-chemical and biological processes. In the marine phreatic environment it represents an essential mechanism for the development and stabilization of carbonate platforms. However, diagenetic cements that developed early in the marine phreatic environment are likely to become obliterated during later stages of meteoric or burial diagenesis. When lithified sediment samples are studied, this complicates the recognition of processes involved in early cementation, and their geological implications. In this contribution, a petrographic microfacies analysis of Holocene Halimeda segments collected on a coral island in the Spermonde Archipelago, Indonesia, is presented. Through electron microscopical analyses of polished samples, this study shows that segments are characterized by intragranular cementation of fibrous aragonite, equant High-Mg calcite (3.9 to 7.2 Mol% Mg), bladed Low-Mg calcite (0.4 to 1.0 Mol% Mg) and mini-micritic Low-Mg calcite (3.2 to 3.3 Mol% Mg). The co-existence and consecutive development of fibrous aragonite and equant High-Mg calcite results initially from the flow of oversaturated seawater along the aragonite template of the Halimeda skeleton, followed by an adjustment of cement mineralogy towards High-Mg calcite as a result of reduced permeability and fluid flow rates in the pores. Growth of bladed Low-Mg calcite cements on top of etched substrates of equant High-Mg calcite is explained by shifts in pore water pH and alkalinity through microbial sulphate reduction. Microbial activity appears to be the main trigger for the precipitation of mini-micritic Low-Mg calcite as well, based on the presumable detection of an extracellular polymeric matrix during an early stage of mini-micrite Low-Mg calcite cement precipitation. Radiocarbon analyses of five Halimeda segments furthermore indicate that virtually complete intragranular cementation in the marine phreatic environment with thermodynamically/kinetically controlled aragonite and High-Mg calcite takes place in about 100 years. Collectively, this study shows that early-diagenetic cements are highly diverse and provides new quantitative constraints on the rate of diagenetic cementation in tropical carbonate factories.