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1.
The process of organomineralization is increasingly well understood with respect to modern carbonate sediments accumulating adjacent to tropical reef atolls and reef caves. Mineralization related to non-living organic substrates results in autochthonous micrite production (‘automicrites’). ‘Automicrites’ are the main constructive element of Lower Cretaceous (Albian) carbonate mud mounds in northern Spain. These slope mud mounds occur within transgressive and early highstand system tracts encompassing several macrobenthic ecological zones. They are clearly separated from the biocalcifying carbonate factory (Urgonian carbonate platforms), in both space and time. Within these build-ups, most ‘automicrites’ were initially indurated and accreted to form a medium-relief growth framework. ‘Automicrites’ have a uniform, presumably high-Mg-calcite precursor mineralogy. They show an inorganic stable-isotope signature (?13C around +3·3‰) within the range of early marine cements, and skeletal compounds lacking major vital effects. Epifluorescence microscopy shows that they have facies-specific fluorescence, which is similar to skeletal compounds of Acanthochaetetes, but clearly different from allomicritic sediment and cements, which are mostly non-fluorescent. The EDTA-soluble intracrystalline organic fraction (SIOF) of Albian automicrites shows an amino acid spectrum that is similar to shallow subsurface samples from their modern counterparts. Gel electrophoresis of the SIOF demonstrates an exclusively acidic character, and a mean molecular size range between 20 and 30 kDa. Experiments in vitro (inhibition tests) indicate that the SIOF has a significant Ca2+-binding capacity. Fluorescence and chemical characteristics of SIOF point to a main substance class, such as humic and fulvic acids, compounds that form from pristine organic matter during early diagenesis. Biomarker analyses provide evidence for the crucial role of biodegradation by heterotrophic microorganisms, but no biomarker for cyanobacteria has been found. Primary sources of organic material should have been manifold, including major contributions by metazoans such as sponges. It is concluded that many carbonate mud mounds are essentially organomineralic in origin and that the resulting fabric of polygenetic muds (‘polymuds’) may represent ancestral metazoan reef ecosystems, which possibly originated during the Neoproterozoic.  相似文献   

2.
Various early Paleozoic (Cambrian Series 3–Middle Ordovician) reefs are found in the Taebaek Group, eastern Korea, located in the eastern margin of the Sino-Korean Block. They occur in every carbonate-dominant lithostratigraphic unit of the group, but their morphology and composition differ markedly. The Daegi Formation (middle Cambrian: Cambrian Series 3) contains siliceous sponge-Epiphyton reefs formed in a shallow subtidal environment, which is one of the earliest metazoan-bearing microbial reefs after the archaeocyath extinction. The Hwajeol Formation (upper Cambrian: Furongian) encloses sporadic dendrolites consisting of Angulocellularia, which developed in a relatively deep subtidal environment, representing a rare deeper water example. The onset of the Ordovician radiation resulted in the formation of microbialite–Archaeoscyphia–calathiid patch reefs in shallow subtidal deposits of the Lower Ordovician Dumugol Formation. Subsequent late Early Ordovician relative sea-level fall established extensive peritidal environments, forming microbial mats and stromatolites of the Lower–Middle Ordovician Makgol Formation. Ensuing Ordovician radiation resulted in one of the earliest metazoan skeletal reefs of the Middle Ordovician Duwibong Formation, constructed by stromatoporoid Cystostroma and bryozoan Nicholsonella, and developed around shallow shoals. These reefs reflect ongoing evolution and sea-level change during the early Paleozoic, and exemplify a rare glimpse of peri-Gondwanan records of reef evolution, which warrant detailed investigations and comparison with their counterparts in other regions.  相似文献   

3.
Distinctive, metre‐scale antiformal structures are well developed in a Famennian carbonate platform in the Chedda Cliffs area of the Lennard Shelf reef complexes. The structures are distinguished by chevron‐shaped crests and thickened cores and contain abundant non‐skeletal allochems (ooids/pisoids, peloids and intraclasts) of silt to pebble size and variably developed laminations and fenestrae. The internal morphology and pervasive occurrence of fenestral clotted and wavy laminated fabrics suggest that these structures are microbial mounds composed of agglutinated stromatolites and thrombolites. Microbial fabrics most probably originated through sediment trapping and binding by microbial mats with early lithification involving microbial calcification and cementation of trapped sediment. The facies and stratigraphic context of the mounds support a shallow subtidal, transitional backreef to reef‐flat setting; however, alone these mounds do not provide unequivocal environmental information. Other large antiformal structures in Famennian platforms on the Lennard Shelf, previously described as tepee structures, show morphological similarities to the Chedda Cliffs mounds, which suggests that these other structures may also be microbial mounds. The presence of microbial mounds in platform successions further highlights the importance of microbial communities in the Lennard Shelf reef complexes.  相似文献   

4.
Abstract In mid‐Middle Cambrian time, shallow‐water sedimentation along the Cordilleran passive margin was abruptly interrupted by the development of the deep‐water House Range embayment across Nevada and Utah. The Marjum Formation (330 m) in the central House Range represents deposition in the deepest part of the embayment and is composed of five deep‐water facies: limestone–argillaceous limestone rhythmites; shale; thin carbonate mud mounds; bioturbated limestone; and cross‐bedded limestone. These facies are cyclically arranged into 1·5 to 30 m thick parasequences that include rhythmite–mound, rhythmite–shale, rhythmite–bioturbated limestone and rhythmite–cross‐bedded limestone parasequences. Using biostratigraphically constrained sediment accumulation rates, the parasequences range in duration from ≈14 to 270 kyr. The mud mounds are thin (<2 m), closely spaced, laterally linked, symmetrical domes composed of massive, fenestral, peloidal to clotted microspar with sparse unoriented, poorly sorted skeletal material, calcitized bacterial(?) filaments/tubes and abundant fenestrae and stroma‐ tactoid structures. These petrographic and sedimentological features suggest that the microspar, peloids/clots and syndepositional micritic cement were precipitated in situ from the activity of benthic microbial communities. Concentrated growth of the microbial communities occurred during periods of decreased input of fine detrital carbonate transported offshore from the adjacent shallow‐water carbonate platform. In the neighbouring Wah Wah Range and throughout the southern Great Basin, coeval mid‐Middle Cambrian shallow‐water carbonates are composed of abundant metre‐scale, upward‐shallowing parasequences that record high‐frequency (104?105 years) eustatic sea‐level changes. Given this regional stratigraphic relationship, the Marjum Formation parasequences probably formed in response to high‐frequency sea‐level fluctuations that controlled the amount of detrital carbonate input into the deeper water embayment. During high‐frequency sea‐level rise and early highstand, detrital carbonate input into the embayment decreased as a result of carbonate factory retrogradation, resulting in the deposition of shale (base of rhythmite–shale parasequences) or thin nodular rhythmites, followed by in situ precipitated mud mounds (lower portion of rhythmite–mound parasequences). During the ensuing high‐frequency sea‐level fall/lowstand, detrital carbonate influx into the embayment increased on account of carbonate factory pro‐ gradation towards the embayment, resulting in deposition of rhythmites (upper part of rhythmite–mound parasequences), reworking of rhythmites by a lowered storm wave base (cross‐bedded limestone deposition) or bioturbation of rhythmites by a weakened/lowered O2‐minimum zone (bioturbated lime‐ stone deposition). This interpreted sea‐level control on offshore carbonate sedimentation patterns is unique to Palaeozoic and earliest Mesozoic deep‐water sediments. After the evolution of calcareous plankton in the Jurassic, the presence or absence of deeper water carbonates was influenced by a variety of chemical and physical oceanographic factors, rather than just physical transport of carbonate muds.  相似文献   

5.
The nature of Phanerozoic carbonate factories is strongly controlled by the composition of carbonate‐producing faunas. During the Permian–Triassic mass extinction interval there was a major change in tropical shallow platform facies: Upper Permian bioclastic limestones are characterized by benthic communities with significant richness, for example, calcareous algae, fusulinids, brachiopods, corals, molluscs and sponges, while lowermost Triassic carbonates shift to dolomicrite‐dominated and bacteria‐dominated microbialites in the immediate aftermath of the Permian–Triassic mass extinction. However, the spatial–temporal pattern of carbonates distribution in high latitude regions in response to the Permian–Triassic mass extinction has received little attention. Facies and evolutionary patterns of a carbonate factory from the northern margin of peri‐Gondwana (palaeolatitude ca 40°S) are presented here based on four Permian–Triassic boundary sections that span proximal, inner to distal, and outer ramp settings from South Tibet. The results show that a cool‐water bryozoan‐dominated and echinoderm‐dominated carbonate ramp developed in the Late Permian in South Tibet. This was replaced abruptly, immediately after the Permian–Triassic mass extinction, by a benthic automicrite factory with minor amounts of calcifying metazoans developed in an inner/middle ramp setting, accompanied by transient subaerial exposure. Subsequently, an extensive homoclinal carbonate ramp developed in South Tibet in the Early Triassic, which mainly consists of homogenous dolomitic lime mudstone/wackestone that lacks evidence of metazoan frame‐builders. The sudden transition from a cool‐water, heterozoan dominated carbonate ramp to a warm‐water, metazoan‐free, homoclinal carbonate ramp following the Permian–Triassic mass extinction was the result of the combination of the loss of metazoan reef/mound builders, rapid sea‐level changes across Permian–Triassic mass extinction and profound global warming during the Early Triassic.  相似文献   

6.
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7.
Carbonate buildups in the Flinders Ranges of mid-Early Cambrian age grew during a period of high archaeocyath diversity and are of two types: (1) low-energy, archaeocyath-sponge-spicule mud mounds, and (2) high-energy, archaeocyath-calcimicrobe (calcified microbial microfossil) bioherms. Mud mounds are composed of red carbonate mudstone and sparse to abundant archaeocyath floatstone, have a fenestral fabric, display distinct stromatactis, contain abundant sponge spicules and form structures up to 150m wide and 80 m thick. Bioherms are either red or dark grey limestone and occur as isolated small structures 2–20 m in size surrounded by cross-bedded calcarenites and calcirudites or as complexes of mounds and carbonate sands several hundreds of metres across. Red bioherms comprise masses of white Epiphyton with scattered archaeocyaths and intervening areas of archaeocyath-rich lime mudstone. Grey bioherms are complex intergrowths of archaeocyaths, encrusting dark grey Renalcis and thick rinds of fibrous calcite cement. The bioherms were prone to synsedimentary fracturing and exhibit large irregular cavities, up to 1.5 m across, lined with fibrous calcite. The buildups are isolated or in contiguous vertical succession. Mud mounds occur alone in low-energy, frequently nodular, limestone facies. Individual bioherms and bioherm complexes occur in high-energy on-shelf and shelf-margin facies. The two types also form large-scale, shallowing-upward sequences composed of basal (deep water) mud mounds grading upward into archaeocyath-calcimicrobe bioherm complexes and bioherms in cross-bedded carbonate sands. The uppermost sequence is capped by ooid grainstone and/ or fenestral to stromatolitic mudstone. The calcimicrobe and metazoan associations form the two major biotic elements which were to dominate reefs throughout much of subsequent Phanerozoic time.  相似文献   

8.
Following introduction of the term ‘nummulite bank’, there has been debate regarding interpretation of these types of deposits as autochthonous (automicrite) or allochthonous (detrital micrite). These banks are made up of large foraminifera and ill‐defined fine‐grained components. The fine‐grained components consist mainly of micrites. The recognition of automicrite has deep implications for the synsedimentary cementation and stabilization of the bank. In order to distinguish between automicrite and detrital micrite, the nanomorphology, geochemistry and organic matter remains in the microfacies of a nummulite bank in the Middle Eocene of Monte Saraceno (Gargano, Southern Italy) were analysed. Optical and scanning electron microscope investigations showed that the micrites have been recrystallized to aggrading microsparite. Epifluorescence observations on selected micrite/microsparite areas with peloidal texture revealed the presence of organic matter. Scanning electron microscope analyses on epifluorescent micrites showed that the microbial peloids have smaller crystal sizes than those in organic matter‐depleted areas. The geochemical characterization of extracted organic matter, performed through the functional group analyses by Fourier transform‐infrared spectroscopy, shows strong prevalence of the aromatic fraction over the aliphatic and carboxylic ones. These characteristics of organic compounds indicate both their thermal maturation and their likely derivation from degradation of bacterial communities. The local presence of peloidal anti‐gravity textures, bright epifluorescence and organic molecules in clotted peloidal areas suggest that the metabolic activity of microbial communities could have induced precipitation of these micrites and, consequently, the syndepositional cementation of the nummulite bank. This type of cementation can rapidly stabilize sediments and promote the depositional bank geometry.  相似文献   

9.
自生泥晶,也称作原地微晶碳酸钙或原地灰泥以区分他生泥晶或异地泥晶,指的是通过无机和/或有机媒介过程作用在原地形成的泥晶碳酸钙。在前人的基础上,对自生泥晶概念的提出和发展进行了概括;对自生泥晶的矿物组成、显微结构、荧光和阴极发光特征进行了总结;对自生泥晶的形成过程和来源（包括生物矿化作用、有机矿化作用和无机沉淀三种方式）进行了探讨;对自生泥晶在不同沉积环境碳酸盐岩中的贡献及其地球化学指示进行了论述;对自生泥晶在地质历史时期的分布做了归纳;最后对自生泥晶的后续研究提出了一些展望。认为正确认识自生泥晶的性质,其形成过程和来源对碳酸盐岩的结构成因分类、地质历史时期生物礁丘的演化和地球化学指示、建筑工程和环境修复、探寻地外生命和油气地质等方面都将产生深远的影响。  相似文献   

10.
Recent studies of continental carbonates revealed that carbonates with similar fabrics can be formed either by biotic, biologically-induced, biologically-influenced or purely abiotic processes, or a combination of all. The aim of this research is to advance knowledge on the formation of carbonates precipitated (or diagenetically altered) in extreme, continental environments by studying biotic versus abiotic mechanisms of crystallization, and to contribute to the astrobiology debate around terrestrial analogues of Martian extreme environments. Both fossil (upper Pleistocene to Holocene) and active carbonate spring mounds from the Great Artesian Basin (South Australia) have been investigated. These carbonates consist of low-Mg to high-Mg calcite tufa. Four facies have been described: (i) carbonate mudstone/wackestone; (ii) phytohermal framestone/boundstone; (iii) micrite boundstone; and (iv) coarsely crystalline boundstone. The presence of filaments encrusted by micrite, rich in organic compounds, including ultraviolet-protectants, in phytohermal framestone/boundstone and micrite boundstone is clear evidence of the existence of microbial mats at the time of deposition. In contrast, peloidal micrite, despite commonly being considered a microbial precipitate, is not directly associated with filaments in the Great Artesian Basin mounds. It has probably formed from nanocrystal aggregation on colloid particulate. Thus, where biofilms have been documented, it is likely that bacteria catalyzed the development of fabrics. It is less certain that microbes induced calcium carbonate precipitation elsewhere. Trace elements, including rare earth element distribution from laminated facies, highlight strongly evaporative settings (for example, high Li contents). Carbon dioxide degassing and evaporation are two of the main drivers for an increase in fluid alkalinity, resulting in precipitation of carbonates. Hence, although the growth of certain fabrics is fostered by the presence of microbial mats, the formation of carbonate crystals might be independent from it and mainly driven by extrinsic factors. More generally, biological processes may be responsible for fabric and facies development in micritic boundstone whilst micrite nucleation and growth are driven by abiotic factors. Non-classical crystallization pathways (aggregation and fusion of nanoparticles from nucleation clusters) may be more common than previously thought in spring carbonate and this should be carefully considered to avoid misinterpretation of certain fabrics as by-products of life. It is proposed here that the term ‘organic-compound catalyzed mineralization’ should be used for crystal growth in the presence of organic compounds when dealing with astrobiological problems. This term would account for the possibility of multiple crystallization pathways (including non-classical crystallization) that occurred directly from an aqueous solution without the direct influence of microbial mats.  相似文献   

11.
Modern Ca:Mg carbonate stromatolites form in association with the microbial mat in the hypersaline coastal lagoon, Lagoa Vermelha (Brazil). The stromatolites, although showing diversified fabrics characterized by thin or crude lamination and/or thrombolitic clotting, exhibit a pervasive peloidal microfabric. The peloidal texture consists of dark, micritic aggregates of very high‐Mg calcite and/or Ca dolomite formed by an iso‐oriented assemblage of sub‐micron trigonal polyhedrons and organic matter. Limpid acicular crystals of aragonite arranged in spherulites surround these aggregates. Unlike the aragonite crystals, organic matter is present consistently in the dark, micritic carbonate comprising the peloids. This organic matter is observed as sub‐micron flat and filamentous mucus‐like structures inside the interspaces of the high‐Mg calcite and Ca dolomite crystals and is interpreted as the remains of degraded extracellular polymeric substances. Moreover, many fossilized bacterial cells are associated strictly with both carbonate phases. These cells consist mainly of 0·2 to 4 μm in diameter, sub‐spherical, rod‐like and filamentous forms, isolated or in colony‐like clusters. The co‐existence of fossil extracellular polymeric substances and bacterial bodies, associated with the polyhedrons of Ca:Mg carbonate, implies that the organic matter and microbial metabolism played a fundamental role in the precipitation of the minerals that form the peloids. By contrast, the lack of extracellular polymeric substances in the aragonitic phase indicates an additional precipitation mechanism. The complex processes that induce mineral precipitation in the modern Lagoa Vermelha microbial mat appear to be recorded in the studied lithified stromatolites. Sub‐micron polyhedral crystal formation of high‐Mg calcite and/or Ca dolomite results from the coalescence of carbonate nanoglobules around degraded organic matter nuclei. Sub‐micron polyhedral crystals aggregate to form larger ovoidal crystals that constitute peloids. Subsequent precipitation of aragonitic spherulites around peloids occurs as micro‐environmental water conditions around the peloids change.  相似文献   

12.
The flanks of Middle Triassic carbonate buildups in the Dolomites show well‐developed clinostratification, with typical angles of 30–40°. This paper focuses on the metre‐scale fabric of these clinoforms and sets these within the context of their large‐scale and microscopic features. Clinoform stratification is caused by fibrous cement crusts, by stylolites paralleling a vague stratification and by pelagic limestone interbedded with the lower portions of the clinoforms. These parts of the clinoforms locally exhibit a boulder fabric. A fracture system, subvertical to clinostratification, is filled by fibrous cements and marine internal sediment. The analysis of clinoform fabric indicates that parts consist of in situ automicrite. Other parts of the clinoforms are made up of breccia. The breccias occur as isolated pockets and lenses with random orientation and dimensions ranging from a few square decimetres to hundreds of square metres. The breccias have gradual contacts with the unbrecciated host rock. Breccia components are mostly angular, show a microfacies similar to that of the unbrecciated host rock and are composed of millimetre‐ to decimetre‐sized particles that generally float in radiaxial‐fibrous cement. Matching grain boundaries are common. Calcite cement typically makes up 20 and 40 vol.% of the brecciated areas. Clinostratification, the fracture system, brecciation and boulder fabric point to gravity induced deformation of in situ flank deposits rather than gravity induced depositional processes. Brecciation appears to result from translational sliding (millimetres to metres) on the steep buildup flanks, which caused fracturing of the vaguely stratified automicrite, followed by displacive growth of fibrous cement. Cementation occurred in a (shallow) burial, marine phreatic environment, because cement clasts are virtually absent from the flank‐derived gravity flows in the adjoining basinal sediments. Displacive cement growth indicates a volume increase of the clinoforms during diagenesis of up to 20–40 vol.% and can account for the local drag of buildup interior limestones. Similarly, the boulder fabric appears to be a diagenetic feature, which resulted from differential settling of incompletely lithified boundstone and grainstone, and the interbedded pelagic limestone.  相似文献   

13.
The Al‐Jawf area of northern Saudi Arabia provides spectacular outcrops of Early Devonian carbonate bioherms in the Wadi Murayr and Dumat Al‐Jandal areas. These carbonate bioherms belong to the Qasr Member of the Late Pragian–Early Emsian Jauf Formation (~405 Ma) and are surrounded by a bioclastic carbonate succession. The Qasr Member is the first major carbonate unit of the Palaeozoic succession in Saudi Arabia that mainly consists of microbialite carbonates and metazoan reefs exhibiting distinct mound features. These bioherm complexes and their associated carbonate facies are pervasively dolomitized. Stratigraphic, petrographic and geochemical analyses were conducted to determine the facies distribution and interpret their depositional and diagenetic processes. A total of 11 facies are identified from a range of depositional environments within a carbonate platform system, ranging from tidal flats, lagoon, shoal, patch reefs to reef front. The main diagenetic processes are carbonate cementation and dolomitization. Dolomitization occurred as both fabric preserved (mostly in grain‐dominated facies) and fabric destructive (mud‐dominated facies). The microbialites and coralline sponges facies show poor reservoir with visual porosity less than 5%, but this succession may have a potential to serve as a good source for the underlying and overlying facies. Ooid and peloidal grainstone facies show fair to good visual porosity that locally exceeds 10% with intergranular porosity as the dominant type. However, in the most studied samples, vuggy and intraparticle porosities are observed as the dominant type. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

14.
Marine microbial communities recorded in the Moroccan Anti‐Atlas were unaffected across the Neoproterozoic–Cambrian transition. A stromatolite‐dominated consortium was replaced at the beginning of the Atdabanian (ca 20 Myr after the Neoproterozoic–Cambrian boundary) by shelly metazoan and thromboid consortia, which contain the oldest biostratigraphically significant fossils of the Moroccan Cambrian. The associated collapse of microbial mat (stromatolitic) growth appears to coincide with a change from pre‐Atdabanian shallow‐water restricted conditions into Atdabanian deeper, open‐sea conditions. It is postulated that this environmental change led to an episode of improved water circulation over carbonate platform interiors, promoting shelly metazoan immigration into the region. The Tiout/Amouslek lithostratigraphic contact in the early Atdabanian marks the end of an episodically unstable seafloor as suggested by the abundance of slumping and sliding structures, and synsedimentary microfaults and cracks recorded in the underlying Tiout Member. Concurrent with the transition is the occurrence of a network of cryptic fissures and cavities that provided habitats for a coelobiontic chemosynthetic–heterotrophic microbial community composed of stromatolitic crusts, Renalcis–Epiphyton–Girvanella intergrowths, and Kundatia thalli. In the overlying Amouslek Formation, archaeocyathan–thromboid reefs were constrained by substrate stability, water depth and subsidence rate. Four reef geometries are distinguished: (i) patch reefs surrounded by shales, (ii) bioherms in which flank beds intercalate laterally with carbonate and shale inter‐reef sediments, (iii) biostromes or low‐relief structures formed as a result of lateral accretion of patch reefs, and (iv) kalyptrate complexes that nucleated because of a marked tendency for aggregation, and in which patch reefs and bioherms occur stacked together bounded by clay–marl–silt seams.  相似文献   

15.
Late Mississippian carbonates in southern Montagne Noire are dominantly domical to laterally‐accreted microbial mounds in some formations, as well as stratiform microbial limestones occurring in hundreds of olistoliths within a flysch basin, constituting pieces of a giant puzzle that are used to help reconstruct a platform in a region that is no longer preserved. Petrographic data of limestone samples from 14 continuous long sections of olistoliths have been analyzed statistically, using multivariate clustering (Q‐mode) of the components/matrix/cement and canonical correspondence analysis that allow the reconstruction of the environmental parameters of carbonate microbial communities in space and time. Clustering analysis separated microbial and non‐microbial facies. The calculation of indices along the various axes from canonical correspondence analysis allows recognition of the controlling factors of the mounds and microbial growth as being turbidity, light penetration, bathymetry and storms. Turbidity and light penetration are the primary factors controlling the morphology of the microbial limestones. Representation of the light penetration and bathymetry indices on the stratigraphical sections defines two vertical environmental gradients. Light penetration can be subdivided into euphotic, euphotic–dysphotic and dysphotic‐aphotic conditions. The representation of the bathymetry allows the subdivision of samples into a deeper outer ramp, external mid‐ramp and internal mid‐ramp. The curve distance from the section base = f (index) suggests a cyclicity for the platform that cannot be compared with the onlap curve defined from other cratonic areas (Moscow Basin), and thus the cyclic succession of the Montagne Noire is interpreted to have been mostly tectonically‐controlled. Integration of the data allowed the reconstruction of the original Mississippian carbonate platform, where, up to the Mikhailovian, it appears to correspond to a platform morphology, with narrow shallow water facies and wide turbiditic systems, whereas the width of shallow‐water settings expanded during the Venevian to the Protvian, forming a ramp or distally‐steepened ramp with widespread microbial limestones.  相似文献   

16.
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   

17.
《Sedimentary Geology》2001,139(3-4):261-283
We have estimated abundance and distribution of automicrite, marine cements and skeletal grains in the Triassic Sella massif, an isolated platform flanked by steep (25–35°) clinoforms. 108 samples were taken at constant intervals from measured sections of the major zones of the platform edifice: the platform top, margin–upper slope, and lower slope. In a first step, carried out in the field and on hand specimen, purely detrital deposits were separated from automicrite facies, i.e. beds with automicrite, cement-filled, primary vugs and admixtures of skeletal carbonate and lithoclasts. In the second step, samples with automicrite facies were thin-sectioned and point counted. The categories used for point counting were (a) automicrite, (b) vugs and cement, (c) microspar or neomorphic spar, (d) skeletal grains and (e) internal sediments. At the platform top 46% of samples are pure detrital deposits, 27% consist of automicrite facies and 27% are too strongly altered by dolomitization to allow classification. At the margin–upper slope 68% of samples consist of automicrite facies, 22% are pure detrital sediments and 10% are strongly altered. At the lower slope 63% are detrital deposits, 10% automicrite facies and 27% are extensively dolomitized. The most important contributors to the automicrite facies are automicrite (41% on the platform top, 29% on the margin–upper slope, 28% on the lower slope) and early marine cement (35% on the platform top, 48% on the margin–upper slope, 27% on the lower slope). The amount of skeletal grains is less than 10%.The automicrite facies stabilized the platform margin and upper slope. Automicrite, abundant early marine cements and micro-organisms such as Tubiphytes, formed a rigid framework, thus substituting for the lack of a metazoan reef. On the upper slopes, the framework of automicrite facies stabilized the slope but intermittently. The automicrite layers are frequently dissected by sediment-filled fractures or are broken into clasts. We assume that they slid on the layers of loose detritus. Bigger slides turned into rubbly debris flows that formed metre-thick breccias at the lower slope and the proximal basin floor. The planar shape and steep angle of the clinoforms indicate that the large-scale geometry of the slope was not controlled by the automicrite but rather by non-cohesive layers of sand and rubble piled up to the angle of repose.The production mode of the Sella is comparable of that of a (mud) mound factory. This factory was highly productive: in 1 Ma, the platform aggraded over 300 m and prograded over 2000 m in all directions.  相似文献   

18.
Microbial deposits at Shark Bay constitute a diverse living microbial carbonate system, developed in a semi‐arid, highly evaporative marine setting. Three tidal flats located in different embayments within the World Heritage area were investigated in order to compare microbial deposits and their Holocene evolution. The stressing conditions in the intertidal–subtidal environment have produced a microbial ecosystem that is trapping, binding and biologically inducing CaCO3 precipitation, producing laminated stromatolites (tufted, smooth and colloform), non‐laminated thrombolitic forms (pustular) and cryptomicrobial non‐laminated forms (microbial pavement). A general shallowing‐upwards sedimentary cycle was recognized and correlated with Holocene sea‐level variations, where microbial deposits constitute the younger (2360 years bp ) and shallower sedimentary veneer. In addition, sediments have been documented with evidence of exposure during the Holocene, from 1040 to 940 14C years bp , when sea‐level was apparently lower than present. Filamentous bacteria constitute the dominant group in the blister, tufted and smooth mat types, and coccus bacteria dominate the pustular, colloform and microbial pavement deposit types. In the subtidal environment within colloform and pavement structures, microbial communities coexist with organisms such as bivalves, serpulids, diatoms, green algae (Acetabularia), crustaceans, foraminifera and micro‐gastropods, which are responsible for exoskeleton supply and extensive bioturbation. The internal fabric of the microbial deposits is laminated, sub‐laminar, scalloped, irregular or clotted, depending on the amount of fine‐grained carbonate and the natural ability of microbial communities to trap and bind particles or induce carbonate precipitation. Nilemah tidal flat contains the thickest (1·3 m) and best‐developed microbial sedimentary system; its deposition pre‐dated the Rocky Point and Garden Point tidal flats, with the most positive isotope values for δ13C and δ18O, reflecting strong microbial activity in a highly evaporative environment. There is an evolutionary series preserved within the tidal flats reflecting relative ages and degree of salinity elevation.  相似文献   

19.
The Mississippian (Early Carboniferous) is generally a period of scarce carbonate buildups in South China. This study documents outcrops of stromatolite mounds at Mengcun and Helv villages, in Laibin City, Guangxi Province, South China. The stromatolite mounds contain various stromatolite morphologies including laminar, wavy-laminar, domal or hemispheroidal, bulbous, and flabellate-growth columns. Intramound rocks are brachiopod floatstone and dark thin-bedded laminated micrite limestone. Individual stromatolites at Mengcun village are generally 3–6 cm thick and morphologically represent relatively shallow-water laminar (planar and wavy-undulated stromatolites) and deeper-water domal, bulbous and columnar forms. Where mounds were formed, the stromatolites continued growing upward up to 60 cm thick. Thrombolitic fabrics also occur but are not common. Stromatolite microscopic structure shows the bulk of the lamination to consist of wavy microbialite and discrete thin micritic laminae. These mounds are intercalated in deep-water fore-reef talus breccia, packstone formed as a bioclastic debris flow and thin-bedded limestone containing common chert layers of the Tatang Formation (late Viséan). Further evidence supporting the deep-water setting of the stromatolite mounds are: (1) a laterally thinning horizon of brachiopod floatstone containing deep-water, small, thin-shelled brachiopods, peloidal micritic sediments and low-diversity, mixed fauna (e.g., thin-shelled brachiopods, tube-like worms and algae) that have been interpreted as storm deposits, (2) common fore-reef talus breccias, (3) lack of sedimentary structures indicating current action, (4) preservation of lamination with sponge spicules, and (5) lack of bioturbation suggesting that the stromatolites grew in a relatively low energy, deep-water setting. The stromatolite mounds are the first described stromatolite mounds in Mississippian strata of South China and contain evidence that supports interpretations of (1) growth history of Mississippian microbial buildups and (2) environmental controls on stromatolite growth and lithification.  相似文献   

20.
The Lower Ordovician La Silla Formation of the Precordillera of west‐central Argentina is part of the west‐facing early Palaeozoic, tropical carbonate platform succession that comprises the core of the Cuyania terrane. Up to 360 m thick, it is exposed in several thrust sheets over a distance of some 250 km along and across depositional strike over a palinspastically unrestored distance of about 35 km. La Silla Formation is a strikingly pure limestone with subordinate finely crystalline dolomite and rare chert. It accumulated on a more or less uniformly subsiding passive margin. Copious precipitation of microcrystalline calcite, probably influenced by microbial activity to varying degrees, led to the generation of peloids, ooids and aggregates of these grains, as well as small amounts of lime mud, intraclasts, stromatolites and thrombolites. Rare bioclasts are limited mostly to scattered gastropods and trilobite sclerites; bioturbation is present locally. The array of carbonate rock types is grouped into eight recurring lithofacies, in order of decreasing abundance: (i) peloidal grainstone; (ii) laminated dolostone; (iii) intraclastic rudstone; (iv) microbial laminite; (v) peloidal packstone; (vi) ooidal grainstone; (vii) thrombolite boundstone; and (viii) mudstone. These facies represent sediments that formed solely in a shallow subtidal marine environment, with no evidence of restricted conditions, hypersalinity or subaerial exposure. No events of eustatic sea‐level change are recorded. By far the dominant facies is grainstone composed of well‐sorted, fine sand‐sized peloids and peloidal aggregates in homogeneous, tabular to gently undulating, medium to thick beds; cross‐lamination is scarce. Clusters of sub‐metre‐sized microbial patch reefs developed sporadically. The shallow platform is envisaged to have been covered by extensive peloidal sand flats and low‐relief banks, and little lime mud was generated. The setting was probably microtidal and may not have been affected by strong trade winds. It was washed by frequent, relatively gentle wave action but without experiencing powerful storms. In the middle member, anomalous lenses of intraclastic rudstone and laminated dolostone occur as graded beds overlying sharply downcut scoured surfaces up to 20 cm deep; these are interpreted to indicate a phase when accretion was punctuated occasionally by tsunamis generated from rift‐faulting seaward of the platform margin. The remarkably uniform peloidal grainstone composition over a broad area shows that, given the appropriate combination of climate, environmental and ecological factors, large portions of some early Palaeozoic platforms were dominated by grainy sediment and remained under well‐agitated conditions within fair‐weather wave‐base, without distinct lateral facies differentiation or tidal‐flat aggradation.  相似文献   

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