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On the basis of ultrastructural, biochemical and genetic studies, bacteria and blue green algae (Kingdom Monera, all prokaryotes) differ unambiguously from the eukaryotic organisms (Fungi, plants sensu stricto) and protists or protoctists, (Copeland, 1956). The gap between eukaryotes and prokaryotes is recognized as the most profound evolutionary discontinuity in the living world. This gap is reflected in the fossil record. Fossil remains of Archaean and Proterozoic Aeons primarily consist of prokaryotes and the Phanerozoic is overwhelmingly characterized by fossils of the megascopic eukaryotic groups, both metazoa and metaphyta. Based on the morphological interpretation of microscopic objects structurally preserved in Precambrian cherts, the time of appearance of remains of eukaryotic organisms in the fossil record has been claimed to be as early as 2.7 · 109 years ago, (Ka?mierczak, 1976). Others suggest chronologies varying between 1.7 to 1.3 · 109 (Schopf et al., 1973) or a time approaching 1.3 · 109 years (Cloud, 1974).There is general agreement that many of the Ediacaran faunas, which have been dated at about 680 m.y. are fossils of megascopic soft-bodied invertebrate animals. Since all invertebrates are eukaryotic, the ca. 680 m.y. date for deposition of these animal assemblages may represent the earliest appearance of eukaryotic organisms. But the question remains as to whether there is definitive evidence for eukaryotic cells before this “benchmark” of the late Precambrian.An excellent discussion of this particular problem as especially relating to acritarchs extending from rocks of Upper Riphean through Vendian and into the basal Cambrian is presented in recent studies by Vidal (1974, 1976) in Late Precambrian microfossils from the Visingsö rocks of southern Sweden.Previous work on the laboratory silicification of wood and algal mat communities (Leo and Barghoorn, 1976) suggested that further analysis of “artificial fossils” might be of aid in the interpretation of fossil morphology toward the ultimate solution of this problem. Thus the procedure developed by one of us (ESB) for laboratory wood silicification was adapted to various smaller objects.By successive immersions of wet cellular aggregates, colonies of various organisms and abiotic organic microspheres in tetraethyl orthosilicate, silicified cells and structures are produced which bear an interesting resemblance to ancient chert-embedded microfossils. Our observation of these microorganisms and proteinoid microspheres silicified in the laboratory as well as of degrading microorganisms, both eukaryotic and prokaryotic, have led us to conclude that many, if not all, of the criteria for assessing fossil eukaryotic microorganisms are subject to serious criticism in interpretation. We studied a large variety of prokaryotic algae, some eukaryotic algae, fungi, protozoa, and abiotic organic microspheres stable at essentially neutral pH. In some cases, degradation and/or silicification systematically altered both size and appearances of microorganisms. By the use of monoalgal cultures of blue-green algae, features resembling nuclei, chloroplasts, tetrads, pyrenoids, and large cell size may be simulated. In many cases individual members of these cultures show so much variation that they may be mistaken as belonging to more than one species. The size ranges for silicified prokaryotic and eukaryotic algae overlap. Several prokaryotes routinely yielded spherical or filamentous structures that resembled large cells. Because of genuine large sizes (e.g., Prochloron), shrinkage, systematic alteration or congregation of unicells to form other structures we find sizes to be of very limited use in determining whether an organism of simple morphology was prokaryotic or eukaryotic. Although some “prebiotic proteinoid microspheres” (of Fox and Harada, 1960) are impossible to silicify with our laboratory methods, those stable at neutral pH (Hsu and Fox, 1976) formed spherical objects that morphologically resemble silicified algae or fungal spores. Many had internal structure. We conclude that even careful morphometric studies of fossil microorganisms are subject to many sources of misinterpretation. Even though it is a logical deduction that eukaryotic microorganisms evolved before Ediacaran time there is no compelling evidence for fossil eukaryotes prior to the late Precambrian metazoans. 相似文献
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Rapid in situ silicification of microbes at Loburu hot springs, Lake Bogoria, Kenya Rift Valley 总被引：1，自引：0，他引：1
Microbial mats, located along the margins of hot-spring pools and outflow channels at Lake Bogoria, Kenya, are commonly silicified forming friable laminated crusts. Columnar microstromatolites composed of silica and calcite are also forming at several springs in sites of oscillating water level or spray. Silicification of the microbes involves impregnation of organic tissue by very fine amorphous silica particles and encrustation by small (< 2 μm) silica spheroids. Rapid silicification of the microbes, which may begin while some are still alive, can preserve sheaths and in some examples, the filaments, capsules and cells. Although this provides evidence of their general morphology, the biological features that are required for taxonomic identifications are commonly poorly preserved.
The silica precipitation results mainly from evaporative concentration and rapid cooling of spring waters that have been drawn upward through the mats and microstromatolites by capillary processes. Almost all the silica at the Loburu springs nucleates on microbial substrates. This affinity of silica for functional groups on microbial surfaces contributes to the rapid silicification of the microbes and their preservation in modern and ancient cherts. 相似文献
The silica precipitation results mainly from evaporative concentration and rapid cooling of spring waters that have been drawn upward through the mats and microstromatolites by capillary processes. Almost all the silica at the Loburu springs nucleates on microbial substrates. This affinity of silica for functional groups on microbial surfaces contributes to the rapid silicification of the microbes and their preservation in modern and ancient cherts. 相似文献
4.
The Tandilia Belt in northeast Argentina includes a Neoproterozoic sequence of sediments (Sierras Bayas Group), in which the Cerro Largo Formation, ca. 750 Ma in age, forms a siliciclastic, shallowing upward succession of subtidal nearshore to tidal flat deposits. Trace fossils Palaeophycus isp. and Didymaulichnus isp. have been described from the upper part of this succession. Specific sedimentary structures consisting of round-crested bulges, arranged in a reticulate pattern, and networks of curved cracks are associated with the trace fossils. These structures are considered to be related to epibenthic microbial mats that once colonized the sediment surface. They reflect stages of mat growth and mat destruction, if compared to analogous structures in modern cyanobacterial mats of peritidal, siliciclastic depositional systems. Also the trace fossils are interpreted as mat-related structures, partly forming components of networks of shrinkage cracks, partly representing the upturned and involute margins of shrinkage cracks or circular openings in desiccating and shrinking, thin microbial mats.
The definition of Didymaulichnus miettensis Young as a Terminal Proterozoic trace fossil is questioned, and it may be considered to interpret the ‘bilobate’ structure as the upturned, opposite margins of microbial shrinkage cracks which have been brought back into contact by compaction after burial. 相似文献
5.
Robert G. Maliva 《Sedimentology》2001,48(4):887-896
Nodular cherts can provide a window on the original sediment composition, diagenetic history and biota of their host rock because of their low susceptibility to further diagenetic alteration. The majority of Phanerozoic cherts formed by the intraformational redistribution of biogenic silica, particularly siliceous sponge spicules, radiolarian tests and diatom frustules. In the absence of a biogenic silica source, Precambrian cherts necessarily had to have had a different origin than Phanerozoic cherts. The Mesoproterozoic Belt Supergroup in Glacier National Park contains a variety of chert types, including silicified oolites and stromatolites, which have similar microtextures and paragenesis to Phanerozoic cherts, despite their different origins. Much of the silicification in the Belt Supergroup occurred after the onset of intergranular compaction, but before the main episode of dolomitization. The Belt Supergroup cherts probably had an opal-CT precursor, in the same manner as many Phanerozoic cherts. Although it is likely that Precambrian seas had higher silica concentrations than at present because of the absence of silica-secreting organisms, no evidence was observed that would suggest that high dissolved silica concentrations in the Belt sea had a significant widespread effect on silicification. The rarity of microfossils in Belt Supergroup cherts indicates that early silicification, if it occurred, was exceptional and restricted to localized environments. The similarity of microtextures in cherts of different ages is evidence that the silicification process is largely controlled by host carbonate composition and dissolved silica concentration during diagenesis, regardless of the source of silica. 相似文献
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《Precambrian Research》1985,28(2):163-173
Eight categories of organic-walled coccoid microfossils in the c. 700-Ma-old Doushantuo Formation are described and named. Of these, one genus and species (Paratetraphycus giganteus) is new. Most of the microfossils are interpreted as being the remains of the Chroococcaceae and are morphologically comparable to those of the 650-Ma-old Yudoma microbiota and the 850-Ma-old Bitter Springs microbiota. These microfossils occur in non-stromatolitic cherts, adding preservational information to the study of Precambrian life. 相似文献
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The source of silica in the formation of the Precambrian laminated cherts has long remained a problem to be solved. Through experiments on cherts and living blue-green algae, the authors found that the collected chert samples probably come from primary deposits, and there is a great biomass of fossil algae in chert, among which the filamentous algae can be compared with the living blue-green algae Oscillatoria, that a higher Pco_2 of the gas would be favourable for the increase of the biomass of living blue-green algae and consequently raises the pH value of the water body; and that lack of free oxygen and a higher concentration of SiO_2 in the water have no apparent influence on the biomass of blue-green algae. Based on the evidence above, a biogeochemical model concerning the origin of Precambrian laminated chert has been set up, in which the. photosynthesis of algae under the presumed atmospheric conditions of the Precambrian might raise the pH value of the water body and promote the dissolution of silicate minerals, thus providing a source of colloid SiO_2 for the formation of Precambrian laminated chert.Furthermore, a simulation experiment device has been designed successfully, which can control the temperature(30 ± 0.5°), Pco_2(50662.5 Pa) and Po_2(about zero Pa) of the gas, the rate of photosynthesis of algae and the movement of the water carrying opal. In the simulation experiments, separate measurements have been made on the rate of photosynthesis of algae, pH value and concentration of SiO_2 of the water body, with the results indicating that under the conditions similar to the presumed Precambrian atmosphere, the photosynthesis of algae can make the pH value of the water body go up steadily to over 9.7, leading to the dissolution of the silicate minerals, with the concentration of SiO_2 measured reaching as high as 84 mg/l. Finally, through the vaporation of water, a phenomenon of colloid floccilation has been observed.The simulation experiment has verified the proposed biogeochemical model illustrating the origin of Precambrian laminated chert. Moreover, the device and method of its kind may also be applied to the research on the relationship of the Precambrian algae with the formation of some other mineral deposits such as of Fe, Mn, U and carbonates. 相似文献
8.
微生物活动导致铁氧化被认为是前寒武纪铁建造和红层形成的重要机制之一,但是地质记录中却鲜有相关证据。针对这一问题,本研究选择华北古元古代末的大红峪组微生物席成因构造(MISS)为研究对象,通过沉积学和矿物学的综合研究,揭示微生物活动在前寒武纪铁循环中的关键作用。研究表明:华北井陉大红峪组发育大量以砂裂为代表的MISS,指示当时潮间带至潮上带广泛发育微生物席;非微生物席层发育大量原位和近距离搬运的海绿石,指示低氧富铁的浅海和孔隙水化学条件,而相邻微生物席层则发生了显著的赤铁矿化,指示相对更氧化的沉积环境。考虑到微生物席层与相邻(厘米级)非微生物席层间微生物活动与矿物组成的明显差异,笔者提出微生物活动可能是导致当时低氧铁化浅海环境局部铁氧化的重要机制。本研究提供了微生物参与Fe2+离子氧化的重要证据,对揭示前寒武纪红层和大规模铁建造形成机制具有启示意义。 相似文献
9.
The Menderes Massif, in western Anatolia, has been described as a lithological succession comprising a basal ‘Precambrian gneissic core of sedimentary origin’ overlain in sequence by ‘Palaeozoic schist’ and ‘Mesozoic-Cenozoic marble’ forming the envelope. The boundary between core and schist envelope was interpreted as a major unconformity, the ‘Supra-Pan-African unconformity’. By contrast, our field observations and geochemical data show that around the southern side of Besparmak Mountain, north of Selimiye (Milas), the protoliths of highly deformed, mylonitized augen gneisses are granitoid rocks intrusive into the adjacent Palaeozoic metasedimentary schists. The field relationships indicate the age of intrusion to be younger than late Permian and there is no evidence for the existence of either an exposed Precambrian basement or the ‘Supra-Pan-African unconformity’ in this sector of the Menderes Massif. 相似文献
10.
Breandán Anraoi MacGabhann 《地学前缘(英文版)》2014,5(1):53-62
The term‘Ediacara Biota’(or many variants thereof)is commonly used to refer to certain megascopic fossils of Precambrian and early Palaeozoic age e but what does the term actually mean?What differentiates a non-Ediacaran‘Ediacaran’and an Ediacaran‘Ediacaran’from an Ediacaran non-‘Ediacaran’?Historically,the term has been used in either a geographic,stratigraphic,taphonomic,or biologic sense.More recent research and new discoveries,however,mean that the term cannot actually be defned on any of these bases,or any combination thereof.Indeed,the term is now used and understood in a manner which is internally inconsistent,and unintentionally implies that these fossils are somehow distinct from other fossil assemblages,which is simply not the case.Continued use of the term is a historical relic,which has led in part to incorrect assumptions that the‘Ediacara Biota’can be treated as a single coherent group,has obscured our understanding of the biological change over the PrecambrianeCambrian boundary,and has confused research on the early evolution of the Metazoa.In the future,the term‘Ediacaran’should be restricted to purely stratigraphic usage,regardless of affnity,geography,or taphonomy;suffcient terminology also exists where reference to specimens on a geographic,taphonomic,or biologic basis is required.It is therefore time to abandon the term‘Ediacara Biota’and to instead treat equally all of the fossils of the Ediacaran System. 相似文献
11.
《Precambrian Research》1982,18(4):367-396
This paper outlines studies of Chinese Precambrian stromatolites, which may be subdivided preliminarily into two ‘stromatolite successions’ and seven assemblages.Secondly, based on Chinese data, stromatolites have undoubted stratigraphic significance for intrabasinal correlation, but it is necessary to depend on some of the ‘bridging elements’ and the ‘related assemblages’, as well as on other methods for interbasinal correlation.Finally, the paper discusses some problems of fossil stromatolites, i.e. the principal classification and the stromatolite cycles. 相似文献
12.
Characterization of the Microbial Dolomite of the Upper Sinian Dengying Formation in the Hanyuan Area of Sichuan Province, China 总被引：1，自引：1，他引：0
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.
M. D. BRASIER 《Geology Today》1985,1(5):141-146
Over the last decade, palaeontologists around the world have been striving to understand one of the most remarkable episodes in the fossil record: the explosive evolution of skeletal fossils around the Precambrian–Cambrian boundary. When examined in the field, the close association of geological and biological events is apparent. An important succession in this respect is the classic Precambrian and Cambrian area of Charnwood–Nuneaton in the English Midlands. Here it can be seen that the boundary also spans a time of major tectonic and oceanographic changes. Could these have contributed to the ‘Cambrian evolutionary explosion’? 相似文献
14.
Pradip Samanta Soumik Mukhopadhyay Anudeb Mondal Subir Sarkar 《Journal of Asian Earth Sciences》2011,40(2):542-549
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
15.
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
16.
The Gunflint microbiota 总被引：1，自引：0，他引：1
The microbiota of the Gunflint Iron Formation (～2 Ga old) is sufficiently great in diversity as to represent a “benchmark” in the level of evolution at a time only somewhat less than intermediate between the origin of the earth and the present.To date, thirty entities from these ～2 Ga old microfossiliferous cherts have been described and all but two systematically categorized. From our continuing detailed study of the Gunflint microbiota (ESB for over 20 years) and, in light of our recent investigations on blue-green algal cell degradation, we conclude that: (1) A considerable number of the taxa systematically described are either of doubtful biological origin, doubtful taxonomic assignment, and/or morphologically indistinguishable from previously described Gunflint microorganisms, (2) The microbiota is wholly prokaryotic.At present, we recognize sixteen taxa falling within three categories: (1) blue-green algae (6 taxa; e.g. Gunflintia minuta); (2) budding bacteria (4 taxa; e.g. Eoastrion simplex); and (3) unknown affinities (6 taxa; e.g. Eosphaera tyleri). Organisms of undoubted eukaryotic affinities have yet to be found in the Gunflint.The Gunflint assemblage includes a high percentage of morphologic entities of obscure taxonomic position.Recently, Walter (1975) and Knoll and Barghoorn (1975) reported Gunflint-type microbiotas of approximately the same age as the Gunflint from two localities in Australia. The dominant morphotypes of the Gunflint microbiota appear to be cosmopolitan and the striking similarity of the three assemblages may strengthen the potential of ancient microbiotas for use in Precambrian biostratigraphy. 相似文献
17.
J. William Schopf 《Precambrian Research》1977,5(2):143-173
Diverse, cellularly preserved microbial communities are now known from stromatolitic sediments of at least twenty-eight Precambrian formations. These fossiliferous deposits, principally cherts and cherty portions of carbonate units, range in age from Early Proterozoic (Transvaal Dolomite, ca. 2250 Ma old) to Vendian (Chichkan Formation, ca. 650 Ma old) and include units from Australia, India, Canada, South Africa, Greenland, the United States and the Soviet Union. More than three-quarters of these microbiotas have been discovered since 1970. Although few, therefore, have as yet been studied in detail, virtually all of the assemblages are known to be dominated by prokaryotic (bacterial and blue-green algal) microorganisms and to contain three major categories of microfossils: spheroidal unicells, cylindrical tube-like sheaths, and cellular trichomic filaments. Analyses of data now available (including measurements of more than 7800 fossil unicells) indicate that each of these three types of microfossils exhibited a gradual, but marked, increase in mean diameter and size range during the Proterozoic and that taxonomic diversity apparently also increased, especially beginning about 1400 Ma ago. Thus, it now seems evident that (i) the microbial components of Proterozoic stomatolitic assemblages have varied systematically as a function of geologic age and that (ii) such communities are both more abundant and more widespread than had previously been recognized. These observations augur well for the future use of such assemblages in Precambrian biostratigraphy. At present, however, data are sufficient to warrant the provisional establishment of only a few microfossil-based subdivisions of the Proterozoic. Such zones, necessarily relatively long-ranging, are here tentatively defined; it is of interest to note that boundaries between certain of these microfossil-based subdivisions appear to coincide, at least approximately, with previously suggested stromatolite-based boundaries. To some extent, therefore, results of this study seem consistent with, and may be supportive of, the concept of stromatolite-based biostratigraphy. At the same time, however, the study seems to indicate that stromatolites of markedly differing age, whether of similar or of dissimilar morphology, were probably formed by distinctly differing microbiotas. Data are as yet insufficient to indicate whether differing types of coetaneous, stratigraphically useful, stromatolites were formed by differing microbial communities and two what extent the “evolution” of stromatolite morphology was a result of the biologic evolution of stromatolite-building microorganisms. There is thus continued need for investigation of the potential biostratigraphic usefulness of stromatolitic microbiotas and, especially, for more effective integration of results of such studies with those available from studies of stromatolites without preserved microbiotas and from studies of the acritarchs preserved in Proterozoic shales. 相似文献
18.
Processes of carbonate precipitation in modern microbial mats 总被引：20，自引：0，他引：20
Christophe Dupraz R. Pamela Reid Olivier Braissant Alan W. Decho R. Sean Norman Pieter T. Visscher 《Earth》2009,96(3):141-162
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
19.
Kurt O. Konhauser Vernon R. Phoenix Simon H. Bottrell David G. Adams & Ian M. Head 《Sedimentology》2001,48(2):415-433
Silicified deposits, such as sinters, occur in several modern geothermal environments, but the mechanisms of silicification (and crucially the role of microorganisms in their construction) are still largely unresolved. Detailed examination of siliceous sinter, in particular sections of microstromatolites growing at the Krisuvik hot spring, Iceland, reveals that biomineralization contributes a major component to the overall structure, with approximately half the sinter thickness attributed to silicified microorganisms. Almost all microorganisms observed under the scanning electron microscope (SEM) are mineralized, with epicellular silica ranging in thickness from < 5 μm coatings on individual cells, to regions where entire colonies are cemented together in an amorphous silica matrix tens of micrometres thick. Within the overall profile, there appears to be two very distinct types of laminae that alternate repeatedly throughout the microstromatolite: ‘microbial’ layers are predominantly consisting of filamentous, intact, vertically aligned, biomineralized cyanobacteria, identified as Calothrix and Fischerella sp.; and weakly laminated silica layers which appear to be devoid of any microbial component. The microbial layers commonly have a sharply defined base, overlying the weakly laminated silica, and a gradational upper surface merging into the weakly laminated silica. These cyclic laminations are probably explained by variations in microbial activity. Active growth during spring/summer allows the microorganisms to keep pace with silicification, with the cell surfaces facilitating silicification, while during their natural slow growth phase in the dark autumn/winter months silicification exceeds the bacteria’s ability to compensate (i.e. grow upwards). At this stage, the microbial colony is probably not essential to microstromatolite formation, with silicification presumably occurring abiogenically. When conditions once again become favourable for growth, recolonization of the solid silica surface by free‐living bacteria occurs: cell motility is not responsible for the laminations. We have also observed that microbial populations within the microstromatolite, some several mm in depth, appear viable, i.e. they still have their pigmentation, the trichomes are not collapsed, cell walls are unbroken, cytoplasm is still present and they proved culturable. This suggests that the bulk of silicification occurred rapidly, probably while the cells were still alive. Surprisingly, however, measurements of light transmittance through sections of the microstromatolite revealed that photosynthetically active light (PAL) only transmitted through the uppermost 2 mm. Therefore the ‘deeper’ microbial populations must have either: (i) altered their metabolic pathways; (ii) become metabolically inactive; or (iii) the deeper populations may be dominated by different microbial assemblages from that of the surface. From these collective observations, it now seems unequivocal that microstromatolite formation is intimately linked to microbial activity and that the sinter fabric results from a combination of biomineralization, cell growth and recolonization. Furthermore, the similarities in morphology and microbial component to some Precambrian stromatolites, preserved in primary chert, suggests that we may be witnessing contemporaneous biomineralization processes and growth patterns analogous to those of the early Earth. 相似文献
20.
贵州瓮安陡山沱期矿化生物群的研究进展和意义 总被引：6，自引：2，他引：6
贵州瓮安陡山沱期矿化（磷酸盐化和硅化）生物群的研究近年来倍受关注，它为研究包括后生动物在内的多细胞生物早期演化提供了十分难得的机遇。最近，由于其中部分磷酸盐化球状化石保存了与某些后生动物胚胎早期发育阶段类似的卵裂特征，被认为是后生动物的休眠卵和胚胎化石。但是，由于至今未发现可靠的囊胚期到原肠胚期和幼体孵化的化石证据，此类化石的动、植物之争一直没有停止。作者近期对该套含磷地层进行了系统的分析研究，除已报道的大量休眠卵和胚胎化石外，还发现保存原肠发育特征的磷酸盐化实体化石、蓝藻细胞集合体、可疑海绵动物化石及类似瓶形的不明化石等。研究表明，陡山沱期矿化生物群具有多样性特征，包含了多种门类的不同类型，是迄今为止全球保存最完好的未元古纪磷质化石库。 相似文献