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1.
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   

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

3.
Late Ordovician coral bioherms in the Lourdes Formation of western Newfoundland exhibit a complex mixing of architectural elements, including framework, boundstone and suspension deposits. The bioherms occur within a narrow (16 m) stratigraphic interval, and a prominent unconformity truncates the interval of bioherm growth and tops of many of the bioherms. The buildups developed along a carbonate ramp. They occur isolated and in groups, individuals in groups are aligned in parallel orientation. The sizes of the bioherms range from small (50–100 cm) coral piles to columnar and dome‐shaped masses (1–15 m); however, topographic relief was never more than ≈1 m. Bioherm construction reflects: (i) stacking of the tabulate coral Labyrinthites chidlensis, and less common stromatoporoids; (ii) accumulation of microbial‐stromatoporoid boundstone and suspension deposits within shelter cavities between corals; and (iii) detrital bioherm‐flank skeletal grainstone beds. Trypanites borings are common in the tops of coral heads. The bioherms exhibit three growth‐development stages: (i) seafloor stabilization, wherein rare, abraded coral colonies lie scattered within pelmatozoan/skeletal grainstone lenses; (ii) colonization, wherein corals (L. chidlensis), rare stromatoporoids (Labechia sp.), and other biota (bryozoans) produced a bioherm overlying the basal sediment base; and (iii) diversification, which is marked by a more diverse range of fauna and flora as well as occurrence of shelter‐cavity deposits. The diversification stage usually makes up more than 70% of a bioherm structure, and, in some defines multiple periods of start‐up and shut‐down of bioherm growth. The latter is defined by bored omission surfaces and/or deposition of inter‐bioherm sediment. The Lourdes bioherms have a similar ecological structure, biotic diversity and depositional environment to patch reefs in the equivalent Carters Limestone in Tennessee. The mixture of coral stacking and boundstone as architectural elements identify an Early Palaeozoic transition of reef‐design development along shallow‐water platforms that began to displace the muddy (boundstone, bafflestone) carbonate buildups more typical of the Early and Middle Ordovician time.  相似文献   

4.
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   

5.
Existing facies models for Devonian reef systems can be divided into high‐energy and low‐energy types. A number of assumptions have been made in the development of these models and, in some cases, criteria that distinguish important aspects of the models are poorly defined. The Upper Devonian Alexandra Reef System contains a variety of reef fabrics from different depositional environments and is ideal for studying the range of environments in which stromatoporoids thrived and the facies from these different environments. A wide variety of stromatoporoid growth forms including laminar, tabular, anastamosing laminar and tabular, domal, bulbous, dendroid, expanding conical, concave‐up whorled‐laminar, concave‐up massive tabular and platy‐multicolumnar are present in the Alexandra Reef System. The whorled‐laminar and massive tabular concave‐up growth forms are virtually undocumented from other Devonian reefs but were common in the reef front of the Alexandra, where they thrived in a low‐energy environment around and below fair‐weather wave base. In contrast, high‐energy parts of the reef margin were dominated by bioclastic rubble deposits with narrow ribbon‐like discontinuous bodies of laminar stromatoporoid framestone. In the lagoon, laminar stromatoporoids formed steep‐sided sediment‐dominated bioherms in response to sea‐level rise and flooding. Relying mostly on the different reef facies in the Alexandra system, a new classification scheme for Devonian reef fabrics has been developed. Devonian reef fabrics can be classified as being: (i) sediment‐laden metazoan dominated; (ii) metazoan–microbial dominated (boundstone); (iii) metazoan dominated (framestone); or (iv) metazoan–marine cement dominated. Distinction of these fabrics carries important sedimentary and palaeoecological implications for reconstructing the depositional environment. With examples from the Alexandra Formation, it is demonstrated that reef facies accumulated in a range of depositional environments and that the simple observation of massive stromatoporoids with or without microbial deposits does not automatically imply a high‐energy reef margin, as otherwise portrayed in a number of the existing facies models for these systems.  相似文献   

6.
梅冥相  张瑞  李屹尧  接雷 《岩石学报》2017,33(4):1073-1093
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   

7.
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   

8.
The Al‐Jawf area of northern Saudi Arabia provides spectacular outcrops of Early Devonian carbonate bioherms in the Wadi Murayr and Dumat Al‐Jandal areas. These carbonate bioherms belong to the Qasr Member of the Late Pragian–Early Emsian Jauf Formation (~405 Ma) and are surrounded by a bioclastic carbonate succession. The Qasr Member is the first major carbonate unit of the Palaeozoic succession in Saudi Arabia that mainly consists of microbialite carbonates and metazoan reefs exhibiting distinct mound features. These bioherm complexes and their associated carbonate facies are pervasively dolomitized. Stratigraphic, petrographic and geochemical analyses were conducted to determine the facies distribution and interpret their depositional and diagenetic processes. A total of 11 facies are identified from a range of depositional environments within a carbonate platform system, ranging from tidal flats, lagoon, shoal, patch reefs to reef front. The main diagenetic processes are carbonate cementation and dolomitization. Dolomitization occurred as both fabric preserved (mostly in grain‐dominated facies) and fabric destructive (mud‐dominated facies). The microbialites and coralline sponges facies show poor reservoir with visual porosity less than 5%, but this succession may have a potential to serve as a good source for the underlying and overlying facies. Ooid and peloidal grainstone facies show fair to good visual porosity that locally exceeds 10% with intergranular porosity as the dominant type. However, in the most studied samples, vuggy and intraparticle porosities are observed as the dominant type. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

9.
A ~6 Ma Messinian (late Miocene) Bioherm Unit on the southern slope of the Sorbas Basin, SE Spain, contains numerous biotically diverse lensoid patch reefs that formed on a shelf to basin slope during a cycle of relative sea-level change. Halimeda reefs are the largest and most complex of the patch reefs and are divisible into core, cap, and flank facies. On the upper and midslope they are up to 40 m thick and 400 m long. They become smaller downslope. The core consists of jumbled Halimeda segments, released by spontaneous disaggregation of the alga. The segments were stabilized close to their sites of growth and rapidly lithified by micritic and peloidal microbial crusts. Residual cavities were further veneered by isopachous marine cements. Flank facies, consisting of bedded packstones to rudstones, form wedge-shaped units lateral to the mounds. Cap facies consist of bioclastic calcarenites/calcirudites and microbial carbonates. Synsedimentary lithification assisted rapid accretion and inhibited off-mound export of sediment. Allochthonous reef-derived blocks on the mid-slope reflect penecontemporaneous rigidity of the Halimeda bioherms. Proximal Porites coral frame patch reefs associated with calcarenites were located near the shelf margin during the initial lowstand stage. Halimeda segment reefs associated with calcarenites and silty marls developed on the midslope and bivalve-bryozoan-serpulid reefs formed on the lower slope in silty marls with occasional turbidites. During the transgressive stage, coral patch reefs near the shelfbreak were overgrown by Halimeda. During highstand progradation, cap facies spread basinward as a sheet connecting many of the midslope patch reefs. These ancient analogues differ from most modern Halimeda reefs in being discrete laterally restricted patch reefs, surrounded by marly sediment, and located on a slope. They are, however, broadly comparable in biota, thickness, and depositional depth. Intense early lithification by microbial crusts and marine cements is an important feature of these Messinian segment reefs. It has not been reported from modern examples.  相似文献   

10.
张俊明  彭克兴 《地质科学》1994,29(3):236-245
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   

11.
Reefal buildups in western Mongolia of mid-Early Cambrian (late Atdabanian) age flourished during a period when shelf seas were globally widespread. The succession at Zuune Arts records the transition from shallow marine siliciclastic sediments (Bayan Gol Formation) to shallow marine, but still clastic-influenced, carbonates (Salaany Gol Formation). The Salaany Gol Formation is interpreted as having been deposited as a series of shallowing upwards cycles on a shallow, gently inclined shelf in a rapidly subsiding epicontinental sea. Cycles commenced with the growth of subtidal metazoan-calcimicrobe aggregative communities on an open shelf. The resultant buildups were commonly engulfed by extensive, massive microbial stromatolites when they grew in agitated intertidal conditions. Latterly, they were smothered by ooid shoals in response to rapid sea level rise. Four types of reefal buildup are distinguished: (1) green-coloured calcimicrobe (Tarthinia, Epiphyton, Gordonophyton and Renalcis) boundstones; (2) red-or green-coloured Cambrocyathellus-Tarthinia-Epiphyton bafflestones; (3) red-coloured Okulitchicyathus bindstones; and (4) red-coloured radiocyath-archaeocyath-cribricyath bioherms. Each is interpreted as having grown at increasing depths and possibly sedimentation rates. The buildups are commonly enclosed within graded and planar bedded bioclastic grainstones and packstones, and are best developed towards the top of the formation, when sea level was high. Thickets of large, solitary archaeocyaths are also inferred in the deeper interbiohermal areas. These buildups had synoptic relief and constructed porous structures with growth-framework cavities housing diverse coelobiontic communities. Extensive synsedimentary cements are present, including pseudomorphed aragonitic fans and possible pseudomorphed aragontic botryoids. These early reefs thus have geological fabrics similar to later Phanerozoic representatives. It is proposed however, that this ecosystem was largely composed of generalist and opportunistic filter and suspension feeders which were dependent upon a far higher input of nutrients than modern day reefal developments. Bacteria were probably the main primary producers, from both planktic and benthic cyanobacterial communities. The diversity of each buildup assemblage appears to be controlled by primary cavity size, the richest fauna belonging to the highly tiered radiocyath-dominated community inferred to have lived in the deepest waters. The communities at Zuune Arts can be compared with other buildups from the early Cambrian, and with Lower Ordovician receptaculid-calcimicrobe-solitary sponge bioherms known from the USA and Siberia.  相似文献   

12.
梅冥相  郭荣涛  胡媛 《岩石学报》2011,27(8):2473-2486
北京西郊下苇甸剖面的崮山组,属于寒武系第三统顶部,自下而上从陆棚相泥灰岩向上变浅至鲕粒滩相灰岩,组成一个淹没不整合型三级沉积层序。在该组上部的一层块状鲕粒滩相颗粒灰岩中,发育串珠状分布的、可以归为叠层石生物丘的穹窿状构造。这些叠层石生物丘,典型的地势隆起和突变的边界代表了明显的早期石化作用特征。叠层石生物丘中的柱状叠层石,为典型的泥晶相叠层石,其内部除了黏结较多的三叶虫生物碎屑外,还不均匀地分布着放射-纤维状方解石(或文石?)组成的底栖鲕粒。这些底栖鲕粒,以其较小的粒径、多样的类型、平滑但不连续的鲕粒圈层以及外部边缘的泥晶套等特征,明显区别于宿主岩石中的颗粒滩相悬浮鲕粒,而且表现出较为明显的与微生物活动相关的微组构。鉴于叠层石是典型的微生物席建造物,该叠层石生物丘特别的宏观和微观沉积组构还可以进一步将其归为较为典型的"微生物礁",从而成为研究中奥陶生物大辐射事件之前贫乏骨骼的浅海环境的沉积作用样式、以及更加深入理解这一特殊时期的微生物造礁作用特征提供了一个较为典型的实例。  相似文献   

13.
《Sedimentology》2018,65(1):303-333
Calathid–demosponge carbonate mounds are a feature of Early to Middle Ordovician shallow‐marine carbonate depositional environments of tropical to subtropical palaeolatitudes. These mounds contain an important amount of autochthonous non‐skeletal microcrystalline calcium‐carbonate (automicrite) conventionally considered microbial in origin. Here, the automicrite of calathid–demosponge carbonate mounds (Tarim Basin, north‐west China) is broken down into five distinct fabrics: an in situ peloidal–spiculiferous fabric (AM‐1), an in situ peloidal fabric (AM‐2), an aphanitic–microtubular fabric (AM‐3), a minipeloidal fabric (AM‐4) and a laminoid–cerebroid fabric (AM‐5). Type AM‐1 occurs with AM‐2 being succeeded by an assemblage of AM‐3 and AM‐4. Types AM‐4 and AM‐5 are separated by an erosional disconformity. A good correlation of fluorescence and cathodoluminescence of automicrites indicates that induced and supported organomineralization produced automicrite, probably via the permineralization of non‐living organic substrates adsorbing dissolved metal–humate complexes. Using a spreadsheet with six parameters and 17 characters, AM‐1 to AM‐4 turn out to be non‐microbial in origin. Instead, these automicrites represent relics of calcified metazoan tissues, such as siliceous sponges, non‐spiculate sponges or the basal attachment structures of stalked invertebrates. Fabric AM‐5 is a microbial carbonate but is post‐mound in origin forming a drape within a reefal framework established by AM‐4. The five automicritic fabrics, individually or as an assemblage, are a common element of Ordovician calathid–demosponge carbonate mounds in general. The reassessment of the origins of these automicritic fabrics holds consequences for understanding of the Great Ordovician Biodiversification Event in terms of community structure, reef ecology and reef evolution. Episodically, these fabrics are also present in other carbonate build‐ups stretching from the Neoproterozoic over the entire Phanerozoic Eon. The massive calcification of metazoan soft tissue (AM‐1 to AM‐4) characterizes episodes and conditions of enhanced marine calcification and might be of value to refine secular trends of p CO2, Ca concentration and Mg/Ca ratio at the scale of individual sedimentary basins.  相似文献   

14.
The complex pattern of biological accretion, internal sedimentation, early lithification, and biological destruction, that characterizes modern reefs and many fossil reefs has been recognized in archaeocyathid-rich patch reefs of Lower Cambrian age in the Forteau Formation, southern Labrador. Patch reefs occur as isolated masses or complex associations of many discrete masses of archaeocyathid-rich limestone and skeletal lime sands, surrounded by well-bedded skeletal limestones and shales. Each reef is composed of many loafshaped mounds stacked on top of one another. The limestone of each mound comprises archaeocyathids and Renalcis or Renalcis-like structures in a matrix of argillaceous lime mud rich in sponge spicules, trilobite and salterellid skeletons. Numerous growth cavities roofed by pendant Renalcis-like organisms and Renalcis are partially to completely filled with geopetal sediment indicating that much of the matrix was deposited as internal sediment. Two stages of diagenetic alteration are recognized: (1) syn-depositional, which affected only the reefs, and (2) post-depositional, which affected both reefs and inter-reef sediments. On the sea floor reef sediments were pervasively cemented and fibrous carbonate was precipitated in intraskeletal and growth cavities. These limestones and cements as well as archaeocyathid skeletons, were subsequently bored by endolithic organisms. Later post-depositional subaerial diagenesis resulted first in dissolution of certain skeletons and precipitation of calcite cement above the water table, followed by extensive precipitation of pore-filling calcite below the water table. These carbonate reefs are similar in structure to the basal pioneer accumulations of much younger lower and middle Palaeozoic reefs. They did not develop into massive ‘ecologic’ reefs because archaeocyathids never developed the necessary large, massive, hemispherical skeletons. This occurrence indicates that reefs developed more or less coincident with, and not long after, the appearance of skeletal metazoans in the Lower Cambrian.  相似文献   

15.
Ancient microbialites reflect interactions between microbial communities and environmental conditions. However, evaluating the relative roles of microbial community processes and environmental influences on microbialite morphology and internal fabric in the rock record can be challenging. The Neoproterozoic Beck Spring Dolomite preserves diverse microbialites, and thus provides an opportunity to explore the factors that influenced microbialite development locally. Stromatolitic, thrombolitic and composite microbialites are abundant in subtidal to upper intertidal carbonates in the Beck Spring Dolomite. Thrombolitic and composite microbialites have not been recognized previously in this unit, but compose much of the newly defined thrombolitic member. Stratigraphic relationships demonstrate that these three types of microbialites formed in close spatial and temporal association in subtidal to intertidal environments. The relative proportions and distributions of stromatolitic and thrombolitic microbialites vary with depositional environment; stromatolitic microbialites dominate in deeper intertidal to subtidal facies, whereas thrombolitic textures are more abundant in upper intertidal facies. Composite microbialites, composed of intermingled clotted and laminated textures, formed in all environments but are most abundant in intertidal facies. The broad environmental distribution of stromatolitic, thrombolitic and composite microbialites and the intermingling of textures suggest that laminated and clotted textures reflect diverse microbial community morphologies rather than environmental variations. Furthermore, the ca 750 Ma age of thrombolitic microbialites in the Beck Spring Dolomite requires that they formed without the influence of calcimicrobes or metazoans colonizing and grazing the microbial mat surface. Thus, these thrombolites provide further evidence that the biostratigraphic distribution of thrombolites cannot be uniquely attributed to evolution of calcifying and grazing organisms in the earliest Cambrian, and that older microbial communities were capable of producing clotted textures.  相似文献   

16.
藏西北三岔口地区泥盆系生物礁特征及其意义   总被引:3,自引:0,他引:3       下载免费PDF全文
在羌塘西部的三岔口一带泥盆系拉竹龙组中发现规模较大的生物礁———台地前缘礁。下层礁体厚7.28m,上层礁体厚40.98m。两个礁体均为叠置礁,礁体由礁基、礁核、礁顶组成。剖面显示发育有礁前垮塌角砾、礁格架、礁间及礁后环境。泥盆纪生物礁的发现为羌塘盆地寻找油气资源提供了新思路。  相似文献   

17.
在羌塘西部的三岔口一带泥盆系拉竹龙组中发现规模较大的生物礁——台地前缘礁。下层礁体厚7.28m,上层礁体厚40.98m。两个礁体均为叠置礁,礁体由礁基、礁核、礁顶组成。剖面显示发育有礁前垮塌角砾、礁格架、礁间及礁后环境。泥盆纪生物礁的发现为羌塘盆地寻找油气资源提供了新思路。  相似文献   

18.
The onset of the Cambrian witnessed the diversification of “small shelly fossils (SSF)”, which affected carbonate depositional system. One of the problematic SSF, chancelloriids, are common components of the early to middle Cambrian carbonate and shale, and their contributions toward Cambrian carbonates are not yet fully understood. This study assesses distribution patterns of chancelloriid sclerites in the Cambrian Series 3 Daegi Formation based on microfacies analysis and discusses their sedimentologic implications. In the lower part of the formation, partially articulated chancelloriid sclerites occur mainly in bioclastic packstone and grainstone facies, with isolated sclerite rays in nodular packstone to grainstone facies. In the middle part of the formation, chancelloriid fragments occur only sporadically in bioclastic wackestone to packstone, bioclastic grainstone and oolitic packstone to grainstone facies, whereas boundstone facies are nearly devoid of their fragments. There are no chancelloriid fragments in the upper part of the formation, which consists of oolitic packstone to grainstone facies. Chancelloriids are interpreted to have primarily occupied platform margin shoal environments, shedding their sclerites to surrounding areas, and thus contributed as sediment producers. The distribution of Daegi chancelloriid sclerites is similar to other Cambrian examples, with the exception of common chancelloriids in Cambrian Series 2 reefs and their apparent near absence in the Daegi and other Cambrian Series 3 reefs. This disparity resulted from changes in the ecologic niche of chancelloriids after the end-Cambrian Series 2 reef crisis, coupled with an overall decline of chancelloriids in the middle Cambrian.  相似文献   

19.
The Lefroy Goldfield in eastern Tasmania is anomalous in southeastern Australia because mineralised fault reefs (i.e. reefs that are also faults) strike in an easterly direction at a high angle to the predominantly northwest strike of bedding and folds. Gold mineralisation is of Early to Middle Devonian age, with reef formation coinciding with a third regionally compressive deformation event (D3), and a second phase of Tabberabberan orogenesis. Mineralised reefs are hosted by Mathinna Supergroup turbidites of Cambrian to Ordovician age and extend for up to 2 km across the boundary between the sandstone‐dominated Stony Head Sandstone and the shale‐dominated Turquoise Bluff Slate. Ore shoots in the reefs plunge moderately west and, in the Volunteer Mine, coincide with the intersection of the reef and a D1/D2 thrust contact. The subvertical orientation and discordant relationship of the mineralised reefs to bedding, as well as the lack of gold mineralisation along bedding and pre‐D3 structures, indicate that the reefs formed during a period of wrench faulting. In contrast to lode‐style deposits in Victoria, the far‐field minimum compressive stress at Lefroy during reef formation was not vertical but, rather, occupied a subhorizontal orientation.  相似文献   

20.
The lower Cambrian Niutitang Formation, a widespread black shale deposition, is of geological interest because of its polymetallic beds, Cambrian explosion, depositional ages, dramatic environmental changes and so on. Previous study focused mainly on inorganic geochemistry and few studies have investigated the organic fractions of upper Neoproterozoic-lower Cambrian strata in South China. Here we report a study of biomarkers plus organic carbon isotopes for black shales from Ganziping, Hunan Province (China). All the saturated hydrocarbon fractions have a unimodal distribution of n-alkanes, a high content of short-chain alkanes and maximize at C 19 or C 20 (C 23 for sample Gzh00-1). The C 27 /C 29 sterane ratio ranges from 0.77 to 1.20 and 4-methylsteranes are in low abundance. These parameters indicate that algae and bacteria are the important primary producers. Furthermore, biomarker maturity proxies show the samples to be higher maturity. The low Pr/Ph values (<0.7) suggest that the samples were deposited under anoxic conditions and, likely, under stratified water columns. In addition, 25-norhopanes and gammacerane are present as diagnostic indicators of normal marine salinity and dysoxic to anoxic conditions. During the Early Tommotian, known to coincide with a transgression event, small shelly fossils increased in abundance and diversity. Moreover, positive δ 13 C org excursions close to 1.4‰ occur at the base of the Tommotian stage. In summary, the Early Cambrian black shales were deposited under dramatic paleoenvironmental changes, including oceanic anoxia, higher primary productivity and sea-level rise.  相似文献   

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