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1.
Ubiquitous microorganisms, especially cyanobacteria preferably grow on the sediment surface thereby producing microbial mats. In the absence of grazers and bioturbators, microbial mat is a unique feature of the Proterozoic. Most of the papers so far published described a wide variety of bed surface microbial mat structures with rare illustrations from sections perpendicular to bedding. Nonetheless, bed surface exposures are relatively rare in rock records. This limitation of bed surface exposures in rock records suggest that a study of microbial mats in bed-across sections is needed. The 60 m thick coastal marine interval of the Sonia Sandstone Formation is bounded between two terrestrial intervals, a transgressive lag at the base and an unconformity at the top, and has been chosen for exploration of microbial mat structures in bed-across sections. A wide variety of microbial mat-induced structures in bed-across sections are preserved within the coastal interval of the Sonia Sandstone. Though many of these structures are similar in some aspects with bed surface structures, some of those presented here are new. The palaeogeographic range of these microbial structures extends from supralittoral to neritic. Diagenetic alterations of microbial mats produce pyrite and those zones are suitable for the preservation of microbial remains. SEM and EDAX analyses show fossil preservation of filamentous microbial remains that confirm the presence of microbial mats within the coastal interval of the Sonia Sandstone. Effects of proliferation of microbial mats in the siliciclastic depositional setting are numerous. The mat-cover on sediment surfaces hinders reworking and/or erosion of the sediments thereby increases the net sedimentation rate. Successive deposition and preservation of thick microbial mat layer under reducing environments should have a great potential for hydrocarbon production and preservation and therefore these Proterozoic formations could be a target for exploration.  相似文献   

2.
Phototrophic mats (microbial mats with a phototrophic top layer) are complex systems in terms of microbial diversity, biogeochemical cycles and organic matter (OM) turnover. It has been proposed that these mats were a predominant life form in Proterozoic shallow water settings, prior to the emergence of bioturbating organisms in the Ediacaran–Cambrian transition. For most of the Precambrian, microbial mats were not only quantitative important carbon fixing systems, but also influenced the transfer and transformation of OM before it entered the geosphere. The profound alteration of compound inventories during transit through microbial mats, implying substantial consequences for OM preservation in the Proterozoic, was recently proposed as a “mat-seal effect” [Pawlowska et al. (2012) Geology 41, 103–106]. To obtain a better understanding of the early diagenetic fate of primary produced OM in microbial mats, we studied a recent calcifying mat from a hypersaline lake in Kiritimati, which showed in the deeper mat layers a maximum 14Ccarbonate age of ∼1500 years. We particularly focused on OM entrapped in the carbonate matrix, because of the better potential of such biomineral-encapsulated OM to reach the geosphere before degradation (and remineralization). Our data indicate that selective preservation is important in phototrophic mats. While a diagenetic transformation of lipid fatty acids (FAs) was evident, their fatty acyl-derived hydrocarbon moieties were not introduced into protokerogen, which was instead mainly comprised of cyanobacterial and/or algal biomacromolecules. Our data support the proposed major impact of the “mat-seal effect” on OM turnover and preservation; i.e. the suppression of biosignatures derived from the upper mat layers, while signals of heterotrophic microbes thriving in deeper mat layers become preferentially preserved (e.g. high hopane/sterane ratios). This mechanism may have broad consequences for the interpretation of biomarkers from Proterozoic shelf environments, because biosignatures of phototrophic mat dwellers as well as planktonic signals may have become heavily biased by the production and turnover of OM in microbial mat systems.  相似文献   

3.
The duration of shoreline occupation at a given sea‐level, coastal response to sea‐level change and the controls on preservation of various shoreline elements can be recognized by detailed examination of submerged shorelines on the continental shelf. Using bathymetric and seismic observations, this article documents the evolution and preservation of an incised valley and lithified barrier complex between ?65 m and ?50 m mean sea‐level on a wave‐dominated continental shelf. The barrier complex is preserved as a series of aeolianite or beachrock ridges backed by laterally extensive back‐barrier sediments. The ridges include prograded cuspate lagoonal shoreline features similar to those found in contemporary lagoons. The incised valley trends shore‐parallel behind the barrier complex and records an early phase of valley filling, followed by a phase of extensive lagoonal sedimentation beyond the margins of the incised bedrock valley. Sea‐level stability at the outer barrier position (ca ?65 m) enabled accumulation of a substantial coastal barrier that remained intact during a phase of subsequent slow sea‐level rise to ?58 m when the lagoon formed. These lagoonal sediments are stripped seawards by bay ravinement processes which caused the formation of several prograded marginal cuspate features. An abrupt rise in sea‐level to ?40 m, correlated with melt‐water pulse 1B, enabled the preservation of thick lagoonal sediments at the top of the incised valley fill and preservation on the sea bed of the cemented core of the barriers. This situation is unique to subtropical coastlines where early diagenesis is possible. The overlying sandy sediment from the uncemented upper portion of the barriers is dispersed by ravinement, partly burying the ridges and protecting the underlying sediments. The high degree of barrier or shoreline preservation is attributed to rapid overstepping of the shoreline, early cementation in favourable climatic conditions and the protection of the barrier cores by sand sheet draping.  相似文献   

4.
In the modern hypersaline carbonate lagoon and sabkha sedimentary environments of Abu Dhabi (United Arab Emirates), three types of organic matter originate respectively from microbial mat, Avicennia mangrove, and Halodule lagoonal seagrass. The study of recent sedimentary processes and cross sections through the sabkha sediments lead to the definition of organo-sedimentary facies based on geochemical and sedimentological criteria. This permits the construction of an organo-sedimentary sequence which expresses the Holocene sedimentary record involving a transgressive and a regressive sequence. The various organic facies occur in both sequences.Heterogeneity within the individual organic facies reflects several factors, including sedimentation dynamics, mineral matrix, oxidation and reduction, and selective organic and mineral diagenesis. These parameters are discussed in terms of depositional environment and location within the organo-sedimentary sequence. Changes in distribution, quantity, and preservation potential of the buried organic matter are discussed in terms of sea level changes and sedimentary accretion rates.  相似文献   

5.
Well-preserved siliciclastic domal stromatolites, up to 2 m wide and 1·5 m high, are found in a 10 to 15 m thick interval within the Late Ordovician Eureka Quartzite of Southern Nevada and Eastern California, USA. These stromatolites appear as either isolated features or patchy clusters that contain more than 70% by volume quartz grains; their association with planar, trough and herringbone cross-bedding suggests that they were formed in an upper shoreface environment with high hydraulic energy. In this environment, sand bars or dunes may have provided localized shelter for initial microbial mat colonization. Biostabilization and early lithification of microbial mats effectively prevented erosion during tidal flushing and storm surges, and the prevalence of translucent quartz sand grains permitted light penetration into the sediment, leading to thick microbial mat accretion and the formation of domal stromatolites. Decimetre-scale to metre-scale stromatolite domes may have served as localized shelter and nucleation sites for further microbial mat colonization, forming patchy stromatolite clusters. Enrichment of iron minerals, including pyrite and hematite, within dark internal laminae of the stromatolites indicates anaerobic mineralization of microbial mats. The occurrence of stromatolites in the Eureka Quartzite provides an example of microbial growth in highly stressed, siliciclastic sedimentary environments, in which microbial communities may have been able to create microenvironments promoting early cementation/lithification essential for the growth and preservation of siliciclastic stromatolites.  相似文献   

6.
Processes of carbonate precipitation in modern microbial mats   总被引:20,自引:0,他引:20  
Microbial mats are ecosystems that arguably greatly affected the conditions of the biosphere on Earth through geological time. These laminated organosedimentary systems, which date back to > 3.4 Ga bp, are characterized by high metabolic rates, and coupled to this, rapid cycling of major elements on very small (mm-µm) scales. The activity of the mat communities has changed Earth's redox conditions (i.e. oxidation state) through oxygen and hydrogen production. Interpretation of fossil microbial mats and their potential role in alteration of the Earth's geochemical environment is challenging because these mats are generally not well preserved.Preservation of microbial mats in the fossil record can be enhanced through carbonate precipitation, resulting in the formation of lithified mats, or microbialites. Several types of microbially-mediated mineralization can be distinguished, including biologically-induced and biologically influenced mineralization. Biologically-induced mineralization results from the interaction between biological activity and the environment. Biologically-influenced mineralization is defined as passive mineralization of organic matter (biogenic or abiogenic in origin), whose properties influence crystal morphology and composition. We propose to use the term organomineralization sensu lato as an umbrella term encompassing biologically influenced and biologically induced mineralization. Key components of organomineralization sensu lato are the “alkalinity” engine (microbial metabolism and environmental conditions impacting the calcium carbonate saturation index) and an organic matrix comprised of extracellular polymeric substances (EPS), which may provide a template for carbonate nucleation. Here we review the specific role of microbes and the EPS matrix in various mineralization processes and discuss examples of modern aquatic (freshwater, marine and hypersaline) and terrestrial microbialites.  相似文献   

7.
Foraminifera can be used to determine the source(s) of carbonate sediment and the directions of sediment transport in shallow, coastal lagoons such as Frank Sound on the south-central coast of Grand Cayman. These determinations, based on the distribution of foraminiferal assemblages and ‘tracer species’ (numerically abundant species that live in known physiographic units and/or ecological conditions), show that the lagoonal sediments are a mixture of grains that originated in the lagoon and forereef. The variable proportions of these foraminifera throughout the lagoon reflects the dynamic processes that control lagoonal sedimentation. Amphistegina gibbosa, Discorbis rosea, and Asterigerina carinata lived in the forereef environment. The fact that these ‘tracer species’ are found throughout Frank Sound and in the beach sands, shows that they were transported across the reef crest and the lagoon. Abrasion-resistant Archaias angulatus, a‘tracer species’ indicative of a lagoonal setting, forms up to 50% of foraminiferal assemblages found in the lagoonal sediments. Preferential winnowing of small tests from these populations indicates sorting under high energy conditions. The vertical distribution of the forereef and lagoonal foraminifera in the sediment blanket that covers the floor of Frank Sound indicates that these processes are temporally persistent. Transportation of forereef foraminifera into and around the lagoon and sorting of the lagoonal foraminifera cannot take place under ‘normal’ conditions when the tranquil lagoon is characterized by weak currents. Storms and/or hurricanes, however, generate short-lived high-energy events that can move and sort the sediment and foraminifera. At the height of a storm, water and sediment are moved over the reef and then piled and held onshore by the onshore winds and the constant flow of water over the reef and across the lagoon. These currents can mix some of the lagoonal and forereef sediments. As a storm wanes, however, the ‘piled water’ flows offshore via strong rip currents that pass into the ocean through the channels which transect the reef. These currents winnow and/or strip sediment from the lagoon and may transport lagoonal sediments into the forereef area. As a result, residual lagoonal sediment is commonly characterized by larger and abrasion-resistant foraminifera.  相似文献   

8.
Abundant scratching traces are described from the Early Triassic Kockatea Shale Formation in the Northampton area of the northern Perth Basin, Western Australia. Except for the Radichnus trace that represents grazing of a possible decapod mecochirids, Scalpoichnus minchinensis igen. and isp. nov. is established to accommodate other scratching sculptures, which might have been produced by arthropods that share similar feeding behaviours to those of decapods. These arthropod traces occurred on a mat‐bound substratum defined by wrinkle structures. Microbial mats may have served as food resources for trace‐makers feeding on the substratum. Furthermore, microbial envelopes functioning as a sole veneer in early diagenesis acted as a crucial role for the preservation of those shallow‐tiered engraving traces. Abundant arthropod traces indicate frequent grazing activities probably by decapods or organisms having similar feeding habits upon microbial mat‐bound substratum, implying that the deposit‐feeders or omnivores survived on the matgrounds in the aftermath of the end‐Permian mass extinction in Gondwanaland. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   

9.
This research provides an ancient analogue for biologically mediated dolomite precipitation in microbial mats and biofilms, and describes the involvement of highly structured extracellular polymeric secretion (EPS) templates in dolomite nucleation. The structure of EPS is shown to match the hexagonal–trigonal lattice geometry of dolomite, which favoured the epitaxial crystallization of dolomite on the organic substrate. This structure of EPS also matches the arrangement of silica nanospheres in opal, which further accounts for the organically‐templated formation of opal enabling the non‐replacive co‐existence of dolomite and silica. The study is focused on a 50 m thick dolomite succession that is exposed in central areas of the Tertiary Duero Basin and was deposited in a mudflat‐saline lake sedimentary complex during the Middle to Late Miocene (9 to 15 Ma). In the intermediate intervals of the succession, poorly indurated dolomite beds pass gradually into silica beds. On the basis of sedimentological, compositional, geochemical and petrographic data, silica and dolomite beds have been interpreted as mineralized microbial mats. The silica beds formed in marginal areas of the lake in response to intense evaporative concentrations; this resulted in the rapid and early precipitation of opal. Silicification accounted for the exceptional preservation of the microbial mat structure, including biofilms, filamentous and coccoid microbes, and EPS. Extracellular polymeric secretions have a layered structure, each layer being composed of fibres which are arranged in accordance with a reticular pattern, with frequent intersection angles at 120° and 60°. Therefore, the structure of EPS matches the lattice geometry of dolomite and the arrangement of silica nanospheres in opal. Additionally, EPS binds different elements, with preference to Si and Mg. The concurrence of suitable composition and surface lattice morphologies in the EPS favoured the crystallization of dolomite on the substrate. In some cases, dolomite nucleation took place epicellularly on coccoid micro‐organisms, which gave way to spheroid crystals. Organic surfaces enable the inorganic mineral precipitation by lowering the free energy barrier to nucleation. Most of the microbial mats probably developed on the lake floor, under sub‐aqueous conditions, where the decomposition of organic matter took place. The subsequent formation of openly packed dolomite crystals, with inter‐related Si‐enriched fibrils throughout, is evidence for the pre‐existence of fibrillar structures in the mats. Miocene dolomite crystals are poorly ordered and non‐stoichiometric, with a slight Ca‐excess (up to 5%), which is indicative of the low diagenetic potential the microbial dolomite has towards a more ordered and stoichiometric structure; this confirms that microbial imprints can be preserved in the geological record, and validates their use as biosignatures.  相似文献   

10.
The microbial community of the flat laminated sediments in the hypersaline lagoon at Laguna Figueroa has undergone dramatic changes due to prolonged periods of submergence under fresh water. This paper describes the techniques used in the first comprehensive in situ ultrastructural study of a stratified microbial community formerly dominated by Microcoleus sp. and introduces the changes caused by flooding and burial. Flat mat desiccation polygons fixed in 2.5% buffered glutaraldehyde were studied by light and transmission electron microscopy. Typical pre-flood Microcoleus-dominated laminated mat from 1977 was compared to post-flood laminated mat from 1979. The technique faithfully preserves the various laminae with their associated organisms and sediment, Morphological identification of several genera of photosynthetic prokaryotes including cyanobacteria, purple, and green bacteria was made by analysis of cell membrane and wall structure. Amoebic cysts could also be recognized in situ. Bacteria of unknown generic affinity, but with distinctive ultrastructure were discovered. A filamentous purple photosynthetic bacterium was found to be a common component of the 1979 mat and two bacteria within a bacterium associations were seen in sections from the 1977 mat.  相似文献   

11.
  rgen Schieber 《Sedimentary Geology》1998,120(1-4):105-124
It has been suspected for some time that microbial mats probably colonized sediment surfaces in many terrigenous clastic sedimentary environments during the Proterozoic. However, domination of mat morphology by depositional processes, post-depositional compaction, and poor potential for cellular preservation of mat-building organisms make their positive identification a formidable challenge. Within terrigenous clastics of the Mid-Proterozoic Belt Supergroup, a variety of sedimentary structures and textural features have been observed that can be interpreted as the result of microbial colonization of sediment surfaces. Among these are: (a) domal buildups resembling stromatolites in carbonates; (b) cohesive behaviour of laminae during soft-sediment deformation, erosion, and transport; (c) wavy–crinkly character of laminae; (d) bed surfaces with pustular–wrinkled appearance; (e) rippled patches on otherwise smooth surfaces; (f) laminae with mica enrichment and/or randomly oriented micas; (g) irregular, curved–wrinkled impressions on bedding planes; (h) uparched laminae near mud-cracks resembling growth ridges of polygonal stromatolites; and (i) lamina-specific distribution of certain early diagenetic minerals (dolomite, ferroan carbonates, pyrite). Although in none of the described examples can it irrefutably be proven that they are microbial mat deposits, the observed features are consistent with such an interpretation and should be considered indicators of possible microbial mat presence in other Proterozoic sequences.  相似文献   

12.
The algal dolostone of the Upper Sinian Dengying Formation (corresponding to the Ediacaran system) in the Upper Yangtze Platform of China possesses a rich diversity of microorganisms and is an ideal site for the study of ancient microbial dolomite. We focused on algal dolostone and its microbial dolomite in the Hanyuan area of Sichuan Province, China. The macroscopic petrological features, microscopic morphology, texture characteristics of the fossil microorganisms and microbial dolomite, and geochemical characteristics were investigated. We found rich fossil microorganisms and microbial dolomites in the laminated, stromatolithic, uniform and clotted (algal) dolostones. The microorganisms present were mainly body fossils of cyanobacteria (including Renalcis, Girvanella, Nanococcus, and Epiphyton) and their trace fossils (including microbial mats (biofilms), algal traces, and spots). In addition, there was evidence of sulfate-reducing bacteria (SRB), moderately halophilic aerobic bacteria, and red algae. The microbial dolomites presented cryptocrystalline textures under polarizing microscope and nanometer-sized granular (including spherulitic and pene-cubical granular) and (sub) micron-sized sheet-like, irregular, spherical and ovoidal morphologies under scanning electron microscope (SEM). The microbial dolomites were formed by microbially induced mineralization in the intertidal zone and lagoon environments during the depositional and syngenetic stages and microbially influenced mineralization in the supratidal zone environment during the penecontemporaneous stage. The microbial metabolic activities and extracellular polymeric substances (EPS) determined the morphology and element composition of microbial dolomite. During the depositional and syngenetic stages, the metabolic activities of cyanobacteria and SRB were active and EPS, biofilms and microbial mats were well-developed. EPS provided a large number of nucleation sites. Accordingly, many nanometer-sized pene-cubical granular and (sub) micron-sized sheet-like microbial dolomites were formed. During the penecontemporaneous stage, SBR, cyanobacteria, and moderately halophilic aerobic bacteria were inactive. Furthermore, nucleation sites reduced significantly and were derived from both the EPS of surviving microorganisms and un-hydrolyzed EPS from dead microorganisms. Consequently the microbial dolomites present nanometer-sized spherulitic and micron-sized irregular, spherical, and ovoidal morphologies. Overall, the microbial dolomites evolved from nanometer-sized granular (including spherulitic and pene-cubical granular) dolomites to (sub) micron-sized sheet-like, irregular, spherical and ovoidal dolomites, and then to macroscopic laminated, stromatolithic, uniform, and clotted dolostones. These findings reveal the correlation between morphological evolution of microbial dolomite and microbial activities showing the complexity and diversity of mineral (dolomite)-microbe interactions, and providing new insight into microbial biomineralization and microbial dolomite in the Precambrian era.  相似文献   

13.
Optical and SEM observations of phosphorites reveal that mineralization is concentrated on ooids and micro-oncoids. The coated grains occur within microbial mats. Microbial mats represent the formational environment of the ooids and oncoids. Both coated grains and mats exhibit similar filamentous micro-organisms. The mat filaments show no fixed orientation and they merge with the concentrically oriented filaments of the coated grains. The branching nature and chlamydospore-like structures of filaments suggest that both mat and coated grains have been formed by fungi. Some coated grains appear to have been slightly disturbed and sometimes mobilized from their sites of formation due to separation from the parent mat resulting perhaps from contraction/fragmentation. The voids so created within the mat had been later filled with either micrite or sparite.  相似文献   

14.
Dinosaur footprints and tracks in the Sousa Basin (Lower Cretaceous, Brazil) occur in at least 37 localities, in distinct stratigraphic positions. Footprints are rare in the Antenor Navarro (lower) and Rio Piranhas (upper) formations, where lithofacies analyses point to sedimentation in ancient alluvial fan to fluvial braided palaeoenvironments. In the Sousa Formation, the generally finer grain sized sediments rendered them more suitable for footprint preservation, where lithofacies analyses point to sedimentation in warm, small/shallow and temporary lakes, swamps and meandering fluvial palaeoenvironments. Microbially induced sedimentary structures are observed in many of the fine-grained lithofacies where dinosaur tracks are also found, and the large number of these tracks in the Sousa Basin (particularly in the Sousa Formation, Lower Cretaceous) may be related to the role of the mats in their preservation. Observations on recent microbial mats show that footprint morphology is related to the mat thickness and to the water content of the mat and the underlying sediment. In dry mats, generally poorly defined or no footprints are produced, while in saturated ones the imprints are well-defined, sometimes with well-defined displacement rims. The formation of well-defined displacement rims around the prints of large dinosaurs occurs in thick, plastic, moist to water-unsaturated microbial mats on top of moist to water-unsaturated sediment. These aspects are commonly observed in the tracks of the Passagem das Pedras site in the Sousa Basin. The footprint consolidation and its early lithification probably occurred due the existence of microbial mats that allowed a more cohesive substrate, preventing the footprints from erosion. The sediments were initially stabilized by early cementation and by the mat fabric over the tracks. Successive flooding, and subsequent sediment influx allowed the large number of layers with dinosaur tracks and sedimentary structures.  相似文献   

15.
The Mesoproterozoic Tieling Formation, near Jixian, northern China, contains thick beds of vertically branched, laterally elongate, columnar stromatolites. Carbonate mud is the primary component of both the stromatolites and their intervening matrix. Mud abundance is attributed to water column ‘whiting’ precipitation stimulated by cyanobacterial photosynthesis. Neomorphic microspar gives the stromatolites a ‘streaky’ microfabric and small mud flakes are common in the matrix. The columns consist of low‐relief, mainly non‐enveloping, laminae that show erosive truncation and well‐defined repetitive lamination. In plan view, the columns form disjunct elongate ridges <10 cm wide separated by narrow matrix‐filled runnels. The stromatolite surfaces were initially cohesive, rather than rigid, and prone to scour, and are interpreted as current aligned microbial mats that trapped carbonate mud. The pervasive ridge–runnel system suggests scale‐dependent biophysical feedback between: (i) carbonate mud supply; (ii) current duration, strength and direction; and (iii) growth and trapping by prolific mat growth. Together, these factors determined the size, morphology and arrangement of the stromatolite columns and their laminae, as well as their branching patterns, alignment and ridge–runnel spacing. Ridge–runnel surfaces resemble ripple mark patterns, but whether currents were parallel and/or normal to stromatolite alignment remains unclear. The formation and preservation of Tieling columns required plentiful supply of carbonate mud, mat‐building microbes well‐adapted to cope with this abundant sediment, and absence of both significant early lithification and bioturbation. These factors were time limited, and Tieling stromatolites closely resemble coeval examples in the Belt‐Purcell Supergroup of Laurentia. The dynamic interactions between mat growth, currents and sediment supply that determined the shape of Tieling columns contributed to the morphotypical diversity that characterizes mid–late Proterozoic branched stromatolites.  相似文献   

16.
《Sedimentology》2018,65(4):1213-1245
In a modern peritidal microbial mat from Qatar, both biomediated carbonates and Mg‐rich clay minerals (palygorskite) were identified. The mat, ca 5 cm thick, shows a clear lamination reflecting different microbial communities. The initial precipitates within the top millimetres of the mat are composed of Ca–Mg–Si–Al–S amorphous nanoparticles (few tens of nanometres) that replace the ultrastructure of extracellular polymeric substances. The extracellular polymeric substances are enriched in the same cations and act as a substrate for mineral nucleation. Successively, crystallites of palygorskite fibres associated with carbonate nanocrystals develop, commonly surrounding bacterial bodies. Micron‐sized crystals of low‐Mg calcite are the most common precipitates, together with subordinate aragonite, very high‐Mg calcite/dolomite and ankerite. Pyrite nanocrystals and framboids are present in the deeper layers of the mat. Calcite crystallites form conical structures, circular to triangular/hexagonal in cross‐section, evolving to crystals with rhombohedral terminations; some crystallite bundles develop into dumb‐bell and stellate forms. Spheroidal organo‐mineral structures are also common within the mat. Nanospheres, a few tens of nanometres in diameter, occur attached to coccoid bacteria and within their cells; these are interpreted as permineralized viruses and could be significant as nuclei for crystallite‐crystal precipitation. Microspheres, 1 to 10 μm in diameter, result from intracellular permineralization within bacteria or the mineralization of the bacteria themselves. Carbonates and clay minerals are commonly aggregated to form peloids, tens of microns in size, surrounded by residual organic matter. Magnesium silicate and carbonate precipitation are likely to have been driven by pH – saturation index – redox changes within the mat, related to microenvironmental chemical changes induced by the microbes – extracellular polymeric substances – viruses and their degradation.  相似文献   

17.
Jonathan Franks  John F. Stolz   《Earth》2009,96(3):163-172
Flat laminated microbial mats are complex microbial ecosystems that inhabit a wide range of environments (e.g., caves, iron springs, thermal springs and pools, salt marshes, hypersaline ponds and lagoons, methane and petroleum seeps, sea mounts, deep sea vents, arctic dry valleys). Their community structure is defined by physical (e.g., light quantity and quality, temperature, density and pressure) and chemical (e.g., oxygen, oxidation/reduction potential, salinity, pH, available electron acceptors and donors, chemical species) parameters as well as species interactions. The main primary producers may be photoautotrophs (e.g., cyanobacteria, purple phototrophs, green phototrophs) or chemolithoautophs (e.g., colorless sulfur oxidizing bacteria). Anaerobic phototrophy may predominate in organic rich environments that support high rates of respiration. These communities are dynamic systems exhibiting both spatial and temporal heterogeneity. They are characterized by steep gradients with microenvironments on the submillimeter scale. Diel oscillations in the physical-chemical profile (e.g., oxygen, hydrogen sulfide, pH) and species distribution are typical for phototroph-dominated communities. Flat laminated microbial mats are often sites of robust biogeochemical cycling. In addition to well-established modes of metabolism for phototrophy (oxygenic and non-oxygenic), respiration (both aerobic and anaerobic), and fermentation, novel energetic pathways have been discovered (e.g., nitrate reduction couple to the oxidation of ammonia, sulfur, or arsenite). The application of culture-independent techniques (e.g., 16S rRNA clonal libraries, metagenomics), continue to expand our understanding of species composition and metabolic functions of these complex ecosystems.  相似文献   

18.
Studies of modern cyanobacterial mats and biofilms show that they can precipitate minerals as a consequence of metabolic and degradational activities paired with ambient hydrochemical conditions. This study looked at modern microbial mats forming giant, tower‐like, groundwater‐fed, calcareous microbialites in the world's largest, highly alkaline lake; Van Gölü (Lake Van), East Turkey. Results show that microbial systems play a role not only in carbonate precipitation but also in the formation of siliceous mineral phases. Transmitted light microscopy, scanning electron microscopy and spectral observations revealed that, within the extracellular polymeric substances excreted by the mats abundant minute aragonite grains precipitated first in vivo. These minute grains were quickly succeeded and/or supplemented in the dead biomass of the cyanobacterial mat by authigenic Al–Mg–Fe siliceous phases. Silicon dioxide is available in large concentrations in the highly alkaline water of Lake Van. Divalent cations (Ca and Mg) are delivered to the microbialites mostly by groundwater springs. The precipitation of the fine‐grained siliceous phases is probably mediated by bacteria degrading the cyanobacterial biomass and complexing the excessive cations with their extracellular polymeric envelopes. The bacteria serve as nucleation centres for the subsequent precipitation of siliceous mineral phases. Generally, the biphasic (calcareous and siliceous) mineralization – characterizing Lake Van microbialites – is controlled by their interior highly dynamic hydrogeochemical situation. There, the dramatically different alkaline lake water and the Ca–Mg‐charged groundwater mix at various rates. The early diagenetic replacement of the in vivo aragonite by authigenic siliceous phases significantly increases the fossilization potential of the mat‐forming cyanobacteria. Lake Van and its giant microbialite tufa towers act as a model explaining the transformation of early diagenetic mineral phases observed in many modern and ancient carbonate marine deposits, particularly those influenced by diffusion of silica‐enriched and metal‐enriched pore waters from below the water–sediment interface.  相似文献   

19.
<正>Microbial mats are ecosystems that can control or induce the precipitation of calcium(Ca) carbonate on Earth through geological time.In the present study,we report on a novel accumulation of Ca,together with iron(Fe),in a microbial mat collected from a slight acidic hot spring(pH=5.9) in south China.Combining an array of approaches,including environmental scanning electron microscopy,X-ray microanalysis,transmission electron microscopy,and selected area electron diffraction,we provide ultrastructral evidence for amorphous acicular aggregates containing Ca and Fe associated with cyanobacteria precipitating in the microbial mats.Cyanobacterial photosynthesis and exopolymeric organic matrixes are considered to be responsible for the precipitation of Ca.These amorphous acicular aggregates might imply the early stage of calcification occurring in microbial mats.Ca and Fe coprecipitation indicates another potential important way of inorganic element precipitation in hot spring microbial mats.Our results provide insight into the possible mechanism of cyanobacterial calcification and microfossil preservation in slight acidic hot spring environments.  相似文献   

20.
Acid-sulfate-chloride (pH∼3) geothermal springs in Yellowstone National Park (YNP) often contain Fe(II), As(III), and S(-II) at discharge, providing several electron donors for chemolithotrophic metabolism. The microbial populations inhabiting these environments are inextricably linked with geochemical processes controlling the behavior of As and Fe. Consequently, the objectives of the current study were to (i) characterize Fe-rich microbial mats of an ASC thermal spring, (ii) evaluate the composition and structure of As-rich hydrous ferric oxides (HFO) associated with these mats, and (iii) identify microorganisms that are potentially responsible for mat formation via the oxidation of Fe(II) and or As(III). Aqueous and solid phase mat samples obtained from a spring in Norris Basin, YNP (YNP Thermal Inventory NHSP35) were analyzed using a complement of chemical, microscopic and spectroscopic techniques. In addition, molecular analysis (16S rDNA) was used to identify potentially dominant microbial populations within different mat locations. The biomineralization of As-rich HFO occurs in the presence of nearly equimolar aqueous As(III) and As(V) (∼12 μM), and ∼ 48 μM Fe(II), forming sheaths external to microbial cell walls. These solid phases were found to be poorly ordered nanocrystalline HFO containing mole ratios of As(V):Fe(III) of 0.62 ± 0.02. The bonding environment of As(V) and Fe(III) is consistent with adsorption of arsenate on edge and corner positions of Fe(III)-OH octahedra. Numerous archaeal and bacterial sequences were identified (with no closely related cultured relatives), along with several 16S sequences that are closely related to Acidimicrobium, Thiomonas, Metallosphaera and Marinithermus isolates. Several of these cultured relatives have been implicated in Fe(II) and or As(III) oxidation in other low pH, high Fe, and high As environments (e.g. acid-mine drainage). The unique composition and morphologies of the biomineralized phases may be useful as modern-day analogs for identifying microbial life in past Fe-As rich environments.  相似文献   

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