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1.
Late Frasnian mounds of the Yunghsien Formation, Guilin, South China, developed as part of the Guilin platform, mostly in reef‐flat and platform margin settings. Microbial mounds in platform margin settings at Hantang, about 10 km west of Guilin, contain Frasnian biota, such as Stachyodes and Kuangxiastraea and, thus, occur below the Frasnian‐Famennian mass extinction boundary. Platform margin facies were dominated by microbes, algae and receptaculitids. Massive corals and stromatoporoids are not common and rarely show reef‐building functions as they did in Givetian time. The margin mounds are composed of brachiopod‐receptaculitid cementstone, and a variety of boundstones that contain Rothpletzella, Renalcis, thrombolite and stromatolite. Other microbial communities include Girvanella, Izhella, Ortonella and Wetheredella. Solenoporoid algae are abundant locally. Zebra structures and neptunian dykes are well‐developed at some intervals. Pervasive early cementation played an important role in lithification of the microbial boundstones and rudstones. Frasnian reefs of many regions of the world were constructed by stromatoporoids and corals, although a shift to calcimicrobe‐dominated frameworks occurred before the Famennian. However, the exact ages of many Frasnian margin outcrops are poorly constrained owing to difficulties dating shallow carbonate facies. The Hantang mounds represent a microbe‐dominated reef‐building community with rare skeletal reef builders, consistent with major Late Devonian changes in reef composition, diversity and guild structure occurring before the end of the Frasnian. A similar transition occurred in the Canning Basin of Western Australia, but coeval successions in North America, Western Europe and the northern Urals are either less well‐known or represent different bathymetric settings. The transition in reef‐building style below the Frasnian‐Famennian boundary is documented here in the two best exposed successions on two continents, which may have been global. Set in the larger context of Late Devonian and Mississippian microbial reef‐building, the Hantang mounds help to demonstrate that controls on microbial reef communities differed from those on larger skeletal reef biota. Calcimicrobes replaced stromatoporoids as major reef builders before the Frasnian‐Famennian extinction event, and increasing stromatoporoid diversity towards the end of the Famennian did not result in a resurgence of skeletal reef frameworks. Calcimicrobes dominated margin facies through the Famennian, but declined near the Devonian‐Carboniferous boundary. Stromatolite and thrombolite facies, which occurred behind the mound margin at Hantang, rose to dominate Mississippian shallow‐water reef frameworks with only a minor resurgence of the important Frasnian calcimicrobe Renalcis in the Visean when well‐skeletonized organisms (corals) also became volumetrically significant frame builders again. 相似文献
2.
Thrombolite fabrics and origins: Influences of diverse microbial and metazoan processes on Cambrian thrombolite variability in the Great Basin,California and Nevada 
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下载免费PDF全文 Thrombolites are a common component of carbonate buildups throughout the Phanerozoic. Although they are usually described as microbialites with an internally clotted texture, a wide range of thrombolite textures have been observed and attributed to diverse processes, leading to difficulty interpreting thrombolites as a group. Interpreting thrombolitic textures in terms of ancient ecosystems requires understanding of diverse processes, specifically those due to microbial growth and metazoan activity. Many of these processes are reflected in thrombolites in the Cambrian Carrara, Bonanza King, Highland Peak and Nopah formations, Great Basin, California, USA; they comprise eight thrombolite classes based on variable arrangements and combinations of depositional and diagenetic components. Four thrombolite classes (hemispherical microdigitate, bushy, coalescent columnar and massive fenestrated) contain distinct mesoscale microbial growth structures that can be distinguished from surrounding detrital sediments and diagenetic features. By contrast, mottled thrombolites have mesostructures that dominantly reflect post‐depositional processes, including bioturbation. Mottled thrombolites are not bioturbated stromatolites, but rather formed from disruption of an originally clotted growth structure. Three thrombolite classes (arborescent digitate, amoeboid and massive) contain more cryptic textures. All eight of the thrombolite classes in this study formed in similar Cambrian depositional environments (marine passive margin). Overall, this suite of thrombolites demonstrates that thrombolites are diverse, in both internal fabrics and origin, and that clotted and patchy microbialite fabrics form from a range of processes. The diversity of textures and their origins demonstrate that thrombolites should not be used to interpret a particular ecological, evolutionary or environmental shift without first identifying the microbial growth structure and distinguishing it from other depositional, post‐depositional and diagenetic components. Furthermore, thrombolites are fundamentally different from stromatolites and dendrolites in which the laminae and dendroids reflect a primary growth structure, because clotted textures in thrombolites do not always reflect a primary microbial growth structure. 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.
An analysis of the development of Late Devonian reefs in a number of regions worldwide shows that reef formation decreased gradually and discontinuously during the second half of the Frasnian and was completely terminated in some places. These events were associated with regression stages. The final Frasnian regression and Kellwasser event, which led to the biotic crisis, resulted, first, in the quantitative reduction of reef formation in the Famennian and, second, in the change of the frame reef formation by the formation of microbial mud mounds in the Famennian. 相似文献
5.
Cryptalgal-metazoan bioherms of early Ordovician age in the St George Group, western Newfoundland 总被引：3，自引：0，他引：3
Bioherms are common in the St George Group, a sequence of shallow-water carbonate rocks deposited on the western continental shelf of Iapetus Ocean. They range from small heads and metre-sized mounds to extensive banks and complexes many metres thick and hundreds of metres in lateral extent. The cores of these bioherms are principally composed of thrombolites (unlaminated, branching, columnar stromatolites), structures quite distinct from laminated stromatolites which are common in intertidal beds. Associated with thrombolites is a diverse fauna of burrowing invertebrates, trilobites, nautiloids, pelmatozoans, brachiopods, gastropods, rostroconchs and archaeoscyphiid sponges. On the basis of framework-building components, three main bioherm types are distinguished: (1) thrombolite mounds, (2) thrombolite-Lichenaria or -sponge mounds and (3) thrombolite-Lichenaria-Renalcis reef complexes. The framework of the last is the most complex, with abundant cavities and a demonstrably uneven growth surface of thrombolites, corals and free-standing Renalcis heads, walls and roofs. Some cavities were active sediment conduits while others were protected, their roofs draped with Renalcis and their walls coated by cryptalgal laminites. These bioherms possess the attributes of shallow-water ecologic reefs. They span a critical time gap in the development of reefs, the transition period from algal-dominated bioherms of the Precambrian and Cambrian to the metazoan-dominated bioherms of the Middle Ordovician and remaining Phanerozoic. 相似文献
6.
Devonian reefs are widespread in the West Canada Basin in three regions: lower Givetian in the north (Elk Point subbasin), upper Givetian and middle Frasnian in the central part (framing of the Peace River Arch), and middle Frasnian (southern end of the basin). Each stage of reef formation ended with regression, and the last reefs terminated long before the Frasnian/Famennian biotic crisis and mass extinction. Reefs of this basin are petroliferous. Moreover, the structure of reservoirs is determined by the reef type, and the highest reservoir properties are related to bioherm varieties in reefs. 相似文献
7.
Messinian stromatolite-thrombolite associations,Santa Pola,SE Spain: an analogue for the Palaeozoic? 总被引：6，自引：0，他引：6
Stromatolite-thrombolite associations are the dominant facies forming large portions of the Santa Pola carbonate platform (SE Spain) during deposition of the Terminal Carbonate Complex (TCC). The TCC, the last period of marine sedimentation in the Western Mediterranean associated with the Messinian Salinity Crisis, comprises a NE-SW trending thrombolite reef with occasionally interlayered stromatolite horizons and a predominantply stromatolite and oolite facies in the back-reef area. The stromatolites are mainly dome shaped, but fine-columnar or wavy-undulose forms can occur. The stromatolites form huge bioherms, extending tens to hundreds of metres. They are finely laminated with alternating layers of dolomicrite and dolomicrospar. The dolomicrite layers appear to be a primary dolomite precipitate, whereas the dolomite crystals in the dolomicrospar layers apparently formed around a meta-stable nuclei which was subsequently dissolved or degraded. The low content of sand-sized particles in the stromatolitic layers indicates formation under low-energy conditions, possibly on a tidal flat. As reported from other areas in the Western Mediterranean, deposition of the TCC at Santa Pola was apparently cyclic, whereby stromatolites generally terminate each depositional cycle. Subtidal Conophyton stromatolites, possibly the only known occurrence younger than Palaeozoic, are, however, found on the reef slope at the base of the first TCC depositional cycle. The dolomitic nature of the unadulterated stromatolitic laminations and the association of stromatolites and thrombolites as platform builders were a common feature in the Early Palaeozoic but are unusual in post-Ordovician carbonate facies. We propose that the conditions during TCC deposition were very restricted, possibly reflecting an environment similar to that of the Early Palaeozoic. 相似文献
8.
Microbial deposits in the aftermath of the end‐Permian mass extinction: A diverging case from the Mineral Mountains (Utah,USA) 下载免费PDF全文
下载免费PDF全文 Emmanuelle Vennin Nicolas Olivier Arnaud Brayard Ivan Bour Christophe Thomazo Gilles Escarguel Emmanuel Fara Kevin G. Bylund James F. Jenks Daniel A. Stephen Richard Hofmann 《Sedimentology》2015,62(3):753-792
The Lower Triassic Mineral Mountains area (Utah, USA) preserves diversified Smithian and Spathian reefs and bioaccumulations that contain fenestral‐microbialites and various benthic and pelagic organisms. Ecological and environmental changes during the Early Triassic are commonly assumed to be associated with numerous perturbations (productivity changes, acidifica‐tion, redox changes, hypercapnia, eustatism and temperature changes) post‐dating the Permian–Triassic mass extinction. New data acquired in the Mineral Mountains sediments provide evidence to decipher the relationships between depositional environments and the growth and distribution of microbial structures. These data also help to understand better the controlling factors acting upon sedimentation and community turnovers through the Smithian–early Spathian. The studied section records a large‐scale depositional sequence during the Dienerian(?)–Spathian interval. During the transgression, depositional environments evolved from a coastal bay with continental deposits to intertidal fenestral–microbial limestones, shallow subtidal marine sponge–microbial reefs to deep subtidal mud‐dominated limestones. Storm‐induced deposits, microbialite–sponge reefs and shallow subtidal deposits indicate the regression. Three microbialite associations occur in ascending order: (i) a red beds microbialite association deposited in low‐energy hypersaline supratidal conditions where microbialites consist of microbial mats and poorly preserved microbially induced sedimentary structure; (ii) a Smithian microbialite association formed in moderate to high‐energy, tidal conditions where microbialites include stromatolites and associated carbonate grains (oncoids, ooids and peloids); and (iii) a Spathian microbialite association developed in low‐energy offshore conditions that is preserved as multiple decimetre thick isolated domes and coalescent domes. Data indicate that the morphologies of the three microbialite associations are controlled primarily by accommodation, hydrodynamics, bathymetry and grain supply. This study suggests that microbial constructions are controlled by changes between trapping and binding versus precipitation processes in variable hydrodynamic conditions. Due to the presence of numerous metazoans associated with microbialites throughout the Smithian increase in accommodation and Spathian decrease in accommodation, the commonly assumed anachronistic character of the Early Triassic microbialites and the traditional view of prolonged deleterious conditions during the Early Triassic time interval is questioned. 相似文献
9.
The Shackleton Limestone formed a carbonate platform that bordered part of the Greater Antarctic craton in middle and late Early Cambrian time. In the Holyoake Range of the central Transantarctic Mountains, this unit records deposition on a stable shelf on which flourished ecological reefs composed of microorganisms and archaeocyathans. Burrow-mottled lime mudstone, wackestone and packstone with patch reefs represent accumulation in shelf areas of relatively low to moderate energy. Thick ooidal grainstone units reflect deposition in higher energy shoals and as sand sheets that were associated with extensive reef complexes. The framework of these reefs was principally the product of micro-organisms, by inference mostly cyanobacteria. Archaeocyathans constitute as much as 30% of some reefs, but commonly they form less than 10% and are absent from some. On the basis of microbial composition, three reef types are recognized. The first type is a Renalcis boundstone that lacks archaeocyathans. Within these, abundant upward-directed thalii of Renalcis formed a framework that trapped fine-grained sediment. The second type, which forms the core of some larger reefs, is composed of stromatactis-bearing, microbial boundstone. The third, yet most common, reef type is variable in composition. It is characterized by the presence of abundant Epiphyton, but may include archaeocyathans, and the microbial microfossils Girvanella and Renalcis as well as cryptomicrobial clotted micrite. In this type of reef, frame-building organisms typically constructed highly porous structures that had small interparticle and fenestral pores and large growth-framework cavities, as well as rare metre-sized caverns. Within these spaces, Epiphyton and, less commonly Renalcis, encrusted framework elements, fine-grained sediments accumulated, and pervasive sea-floor cements were precipitated. Boundstone fabrics in the Shackleton Limestone are highly complex, with fabrics analogous to younger, more metazoan-rich reefs, as well as deep-water stromatactis-bearing mud-mounds. The Epiphyton-Girvanella-archaeocyathan frameworks and stromatactis-bearing boundstones, both of which seemingly first appeared in the middle Early Cambrian, are regarded as the precursors, in structure, composition, and preferred hydrologic setting, of the more extensive reefs and complex framework styles of later Phanerozoic time. 相似文献
10.
J. JAVIER ÁLVARO† SÉBASTIEN CLAUSEN† ABDERRAZZAK EL ALBANI‡ EL HASSANE CHELLAI§ 《Sedimentology》2006,53(1):35-53
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
11.
The Messinian (Late Miocene) marine stratigraphic record of the Sorbas Basin (S.E. Spain) is well preserved and can be considered as being representative of the entire western Mediterranean. It exhibits a series of features relating to: (1) the composition, characteristics and evolution of coral reefs; (2) changes between temperate and subtropical climates; and (3) the extensive development of microbial carbonates (stromatolites and thrombolites) at the end of the Messinian. Each of these features has global significance.
Porites, which is the major and almost only coral component in reefs, is heavily encrusted with stromatolites. These reefs grew at the edge of the subtropical belt and were totally eliminated at the end of the Messinian because of global cooling.
Lowermost-Messinian carbonate sediments in the Sorbas Basin reflect a temperate climate, whereas those immediately above, which contain bioherms and coastal reefs, are subtropical. The shift from temperate to subtropical conditions during the early Messinian was accompanied by an important change in water circulation within the western Mediterranean. Temperate times were marked by cold surface Atlantic waters entering the Mediterranean, whereas subtropical times coincided with warm surface waters entering the western Mediterranean from the east. The subtropical waters were thermally stratified, which favoured the deposition of euxinic marls and diatomites at the centre of the basin. The upwelling of nutrient-rich water promoted stromatolite development within reefs and Halimeda growth on adjacent slopes.
Lastly, microbial carbonates (stromatolites and thrombolites) attained giant dimensions during the late Messinian, which can be regarded as a measure of their success in occupying a variety of ecological niches. This abundance of available habitats is believed to have resulted from the Messinian “salinity crisis”, which was followed by a re-colonization of the western Mediterranean. In this context stromatolite proliferation was due to opportunism of microbial communities in colonizing the new environments, rather than to a complete absence of other competitive biota. We do not believe that hypersaline conditions were a causal factor in stromatolite development because of the normal-marine biota associated with them. 相似文献
12.
LEE Jeong-Hyun HONG Jongsun WOO Jusun OH Jae-Ryong LEE Dong-Jin CHOH Suk-Joo 《《地质学报》英文版》2016,90(1):352-367
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
13.
The framework‐building stromatoporoid Stachyodes, the encrusting calcimicrobe Rothpletzella and encrusting Graticula‐like red algae are major contributors to red algal–calcimicrobial–stromatoporoid bindstones in the Lower Devonian Elmside Formation of the Yass Basin, New South Wales, Australia. The distribution and accumulation patterns of encrusting organisms within the red algal–calcimicrobial–stromatoporoid bindstones observed by optical microscopy and SEM imply a biotic interrelationship between skeletal organisms and microbes that reflects environmental changes. Rothpletzella is characterized by prostrate filaments with frequent branching and a high angle of bifurcation. Filaments of Graticula‐like red algae exhibit rare branching and a relatively low angle of bifurcation. In addition, they are prostrate at the base before becoming erect. Both Rothpletzella and the red algae successively encrust the surfaces of skeletal frameworks, but exhibit different distributions. Rothpletzella and other calcimicrobes cover both the lower and upper surfaces of frameworks, whereas red algae are limited to the upper surfaces. Their individual distributions are thus significantly influenced by the frameworks formed by the thin, laminar stromatoporoid Stachyodes, which create different microenvironments as by‐products. The limited distribution of the red algae was probably related to light levels or phototropism. Upper framework surfaces are variously encrusted by calcimicrobes and the red algae to form thick crusts with varying accumulation patterns. Micritization around the algal thalli, covering of calcimicrobes such as Wetheredella, and microbial micrites between algal thalli all suggest interruptions of algal growth that correspond to episodes of harsh environmental conditions. Transitions from Graticula‐like red algae to Rothpletzella reflect periods of deteriorating environmental change for skeletal organisms, which resulted in the predominance of microbial growth. In contrast, a resurgence of red algae on calcimicrobes suggests improved environmental change. Repeated accumulation patterns between Graticula‐like red algae and Rothpletzella indicate changing habitat environments and competitive relations within skeletal organisms and microbes. These relationships provide insight into understanding how skeletal organisms and microbes utilized space and how they interrelated with each other to produce Devonian reefal limestones. 相似文献
14.
Stromatolitic crusts on stick-like and platy Porites corals forming Messinian reefs in Almería played an important role in supporting and binding the brittle corals. The crusts were previously regarded as probable marine cements. However, their clotted, peloidal, and micritic fabrics are directly comparable with those of stromatolites. They accreted allochthonous grains even on vertical faces, and include bushy fabrics closely comparable with those produced by cyanobacterial calcification. They contain numerous fenestrae, exhibit rapid fabric variation, and locally form micro-columns and laminated domes. Their similarities to peloid micrite crusts in Recent reefs suggest that at least some of these Recent crusts are microbial in origin, even though they have widely been interpreted as marine cements. The sedimentary effects of crust development substantially affected both the morphology and relief of the reefs and the generation of reefal clasts. Binding of the reef-frame in the Pinnacle and Thicket zones in the lower and middle parts of the reef created a rigid margin which shed large (commonly up to 5 m) cuboidal blocks of coral-stromatolite frame. The blocks broke along planes of weakness provided by the vertical Porites sticks and were deposited on the Fore-Reef Slope. In the uppermost parts of the reefs crusts dominate the structure, constituting 80% or more of the rock. Veneers up to 15 cm thick encrust thin irregular Porites plates to create a solid Reef Crest Zone which has not been recognized before. The coral-stromatolite framework is associated with echinoids, crustose corallines and halimedacean algae which, together with the scleractinians, indicate normal marine salinity throughout reef growth. 相似文献
15.
首次系统性地对湖北松滋地区下奥陶统微生物岩开展研究。根据微生物岩的生长方式,文中将微生物岩划分为原地生长型和非原地生长型两大类别,前者包括叠层石、凝块石,后者主要为核形石。根据几何形态特征,将研究区的叠层石分为层状、波状、柱状和丘状4种类型,新发现并命名了双锥柱状叠层石。将凝块石划分为斑状、网状和条带状3种类型,在豹斑状和网状凝块石中,发现了许多钻孔捕食软体动物Ecculiomphalus化石以及生物扰动的痕迹,文中认为这两种凝块石均属于生物扰动型凝块石。生物扰动型凝块石的发现不仅填补了国内、外奥陶纪该领域的部分空白,而且为凝块石成因的研究提供新的材料。在对各类微生物岩的沉积特征分析基础上,阐述了各类微生物岩的沉积环境,并总结其沉积环境分布模式。对微生物岩发育与中奥陶世后生动物大辐射之间的关系进行了探讨,根据早奥陶世晚期至中奥陶世初期后生动物的阶梯式和快速辐射与微生物岩突然减少的对应关系,结合研究区叠层石、凝块石中发现许多后生底栖钻孔捕食腹足类Ecculiomphalus化石等现象,认为微生物岩随时间推移而逐渐减少、衰退与后生动物丰度的快速增加有一定关系,指出食草动物不仅啃食了形成叠层石的菌藻类微生物,造成叠层石数量的不断减少,而且破坏了叠层石的生长状态,结果形成了研究区独具特征的生物扰动型凝块石。此外,作者认为,中奥陶世开始,海平面的快速上升也是研究区微生物岩减少直至消失的原因之一。 相似文献
16.
王家坪古杯礁丘是由不规则古杯和蓝绿藻Renalcis、Epiphyton、Cirvanella等组成的障积礁丘。可分为:孤立小型古杯泥丘和由丘状藻-古杯粘结岩叠置而成的点礁。以Renalcis为主的藻-古杯粘结岩与孤立小型古杯泥丘一样形成于风暴浪基面之下的低能陆架。以Epiphyton为主的藻-古杯粘结岩形成于较动荡的中-高能陆架浅滩。除造礁生物的沉积作用外,早期海底胶结作用和充填固化作用对古杯礁丘的形成亦起了十分重要的作用。 相似文献
17.
Stromatactis‐bearing mud‐mounds remain an enigmatic reef type despite being common in Palaeozoic ramp settings. Two well preserved Upper Devonian (Frasnian) mud‐mounds in the Mount Hawk Formation crop out side by side in the southern Rocky Mountains of west‐central Alberta and provide an opportunity to develop a new case study that can be compared with the other coeval examples, such as those well‐known ones in southern Belgium, as well as evaluate competing hypotheses for mud‐mound formation. The southern mud‐mound is 46·2 m thick and 38·6 m wide at the base, whilst the northern one is 53·3 m thick and 72·2 m wide at the base, and they exhibit three or four growth stages indicated by interfingering and onlapping geometries with flanking strata. The biota is diverse, but fossils only occupy 10·7% by volume, among which sponge spicules, echinoderms, ostracods, brachiopods and calcimicrobes belonging to Girvanella and Rothpletzella are the most common. Five microfacies are discriminated in the mud‐mounds: biomicrite, clotted micrite, spiculite, stromatolite and laminite, with clotted micrite comprising the largest proportion. There is no internal vertical or lateral palaeoecological zonation, and the presence of calcimicrobes and calcareous algae throughout indicates accretion entirely within the photic zone, in a deeper ramp setting seaward of a large carbonate platform to the east. Stromatactis is abundant and the cavities were mostly due to excavation by currents rather than physical collapse of spiculate siliceous sponges. Formation of lime mud involved a combination of multiple organisms, mechanisms and processes. Cyanobacteria were integral to mud‐mound frame‐building and accretion because they stabilized the surface, often permineralized to form Girvanella and provided organic matter that was decomposed by bacteria. This induced precipitation of micrite, forming early indurated rigid masses, evidenced by the presence of intraclasts, stromatactis cavities, isopachous marine cements, absence of bioturbation and rare synsedimentary brittle deformation. The same microbial components, invertebrate biota and clotted micrite occur in underlying strata, suggesting that there was a protracted period of potential mud‐mound initiation before the exact conditions arose to trigger it. The ramp setting, antecedent sea floor topography and relative sea‐level likely contributed together to control this. This study indicates that mud‐mound formation was controlled by a combination of processes, but they are essentially a microbial buildup. 相似文献
18.
华北地台东北缘寒武系芙蓉统叠层石生物丘中的钙化蓝细菌 总被引：5，自引：0，他引：5
华北地台东北缘的芙蓉统,大致为长山组和凤山组所组成,可以进一步划分为3个三级沉积层序;层序划分主要基于沉积相序列的旋回性所代表的沉积趋势,较深水的陆棚相钙质泥岩和深缓坡相条带状泥晶灰岩和泥灰岩组成的凝缩作用序列、与高水位体系域和强迫型海退体系域的中至浅缓坡相碳酸盐岩组成的总体向上变浅序列,是这些三级沉积层序的基本构成,从而形成了较为典型的淹没不整合型层序。那些典型的叠层石生物丘,类似于微生物礁,主要发育在长山组和凤山组下部构成的三级层序的强迫型海退体系域之中,代表了缓坡型台地中相对海平面下降阶段的沉积记录。这些叠层石生物丘中的叠层石,泥晶和微亮晶是其基本构成,最为特征的是发育着一些典型的钙化蓝细菌化石,表明了这些寒武纪芙蓉世的叠层石生长于蓝细菌主导的微生物席的钙化作用之中。最为重要的是,在构成叠层石生物丘的粗糙纹层柱状和穹窿状叠层石中,较为普遍地发育着"石松藻(Lithocodium)";这种谜一样的钙化蓝细菌化石,与其他的钙化蓝细菌化石一起,表明了寒武纪叠层石形成过程中复杂的微生物沉淀作用,成为窥视叠层石生长和石化过程中重要的微生物作用信号。就像其名称所蕴含着的高级绿藻中的松藻(Codium)的涵义一样,"石松藻(Lithocodium)"状的钙化蓝细菌,多描述于中生代的微生物碳酸盐岩中,而且还常常被解释为结壳状有孔虫或"海绵骨针的网状物",其生物亲和性还存在着剧烈的争论。因此,华北地台东北缘寒武系芙蓉统中的叠层石生物丘,特殊的层序地层位置代表了较为典型的强迫型海退沉积记录,特别的钙化微生物构成代表着叠层石生长和石化过程中复杂的微生物作用信号,成为深入了解"寒武纪-早奥陶世微生物碳酸盐岩复苏期"和"显生宙早期第一幕蓝细菌钙化作用事件"中的微生物造礁和成丘作用的典型实例。 相似文献
19.
Devonian sediments of the Malaguide Complex potentially could include the Frasnian–Famennian boundary, one of the five greatest Phanerozoic biotic crises. Conodont biofacies and microfacies of carbonate clasts from a pebbly mudstone underlying Tournaisian radiolarites allows identification, for the first time in the Malaguide Complex, of Devonian shallow marine environments laterally grading to deeper realms. The clasts yielded Frasnian conodont associations of the falsiovalis to rhenana biozones, with six biofacies that reveal different environmental conditions in their source areas. Source sediments were dismantled and redeposited within the pebbly mudstone, whose origin is tentatively related to one of the events that are associated worldwide with the Frasnian–Famennian crisis. The latter is recorded, in two equivalent Malaguide pelagic successions, by stratigraphic discontinuities, and it was, probably, tectonically and/or eustatically controlled, as in other Alpine‐Mediterranean Paleotethyan margins. 相似文献
20.
A Study of Devonian Reefs from Southern China 总被引：2，自引：0，他引：2
G.FLAJS 《《地质学报》英文版》2000,74(4):727-739
Three Devonian reefs (bioherms) from Yunnan and Guangxi, southern China, are studied in detail. Six microfacies types are differentiated. Colonial rugose corals (Columnaria, Disphyllum and Hexagonaria) at Qujing, tabulate corals (Alveolites) with massive stromatoporoids (Actinostroma and Stromatoporella) and sponges at Panxi, and massive stromatoporoids (Actinostroma, Trupetostroma and Stromatoporella) at Yangshuo belong to the most important reef builders. All the three reefs studied clearly reveal a successive evolution history. They developed on the carbonate banks, shallow carbonate platforms and platform margins in the Late Givetian and terminated in the Frasnian due to sea-level falls related to local uplifts of platforms. This coincides with a eustatic fall of relative sea level at the Frasnian/Famennian transition. 相似文献