湖北宜昌王家坪下寒武统天河板组古杯礁丘及其成岩作用

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。     

Facies distribution of the Lower Cambrian cryptic microbial and epibenthic archaeocyathan-microbial communities, western Anti-Atlas, Morocco

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.     

Reefs in the Early Paleozoic Taebaek Group, Korea: A Review

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.     

Facies architecture of a Lower Cretaceous coral-rudist patch reef, Arizona

The Lower Cretaceous Mural Limestone marks the maximum marine incursion into southeast Arizona during Aptian-Albian time and records the middle Cretaceous transition from coral-dominated to rudist-bivalve dominated reefs. Upper Mural Limestone facies are most often dominated by corals. However, rudists form significant frameworks at some localities, one of which is described in this paper. The paleoenvironmental distribution of three potential reef-builders (corals, rudists, and ‘oysters’) were studied at this patch reef locality. Corals built the framework of the inner reef core. The rudist Petalodontia initially gained a foothold in sheltered areas among corals and subsequently built a framework in the outer reef core. Caprinid rudists formed mounds in the outer reef to back reef areas. The rudists Toucasia and Monopleura and the oyster-like bivalve Chondrodonta formed beds or were scattered in the reef-flank and shelf lagoon sediments and did not contribute to the reef framework.Upper Mural Limestone reefs are important examples of the coexistence of corals and rudists during this middle Cretaceous faunal transition period. This study supports the idea that rudist-bivalves initially colonized protected back-reef areas early in the Cretaceous and only later in the Cretaceous did rudists dominate reef frameworks.     

Lower Cambrian patch reefs and associated sediments: southern Labrador, Canada

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.     

Cryptalgal-metazoan bioherms of early Ordovician age in the St George Group, western Newfoundland

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.     

Reef Fabrics, biotic crusts and syndepositional cements of the Latemar reef margin (Middle Triassic), northern Italy

The Latemar reef buildup of the central Dolomites (northern Italy) provides a rare opportunity to examine an in-place Middle Triassic (Upper Anisian to Lower Ladinian) platform margin that is not strongly deformed or dolomitized. The margin lies between the flat lying platform interior and steeply dipping foreslope clinoforms. Across this transition, the depositional profile relates directly to a consistent lateral facies pattern: (1) restricted-biota grainstone of the platform interior, (2) ‘Tubiphytes’-rich boundstone and (3) diverse-biota grainstone that grades into (4) foreslope breccia beds. The boundstone and diverse-biota grainstone facies comprise the platform margin. The boundstone facies consists of a framework of small (< 10 cm) skeletal remains (< 10% by volume) with associated biotic crusts, internal sediments and syndepositional cements. Crusts and cements constitute most of the rock volume and created the boundstone fabric. Biotic crusts exhibit gravity-defying geometries and range from a light grey, ‘structure grumeleuse’ rind to dark grey, micritic laminae. Both cements and biotic crusts occur as redeposited talus in the foreslope talus deposits, indicating a syndepositional origin. The diverse-biota grainstone facies primarily consists of skeletal-peloidal grainstone with a diverse open marine biotic assemblage, in contrast to the restricted biota grainstones of the platform interior that have a low diversity, restricted marine biota. Metre scale hexacoral boundstone and centimetre-scale sponge boundstone and microbial boundstone occur as isolated patches (tens to hundreds of metres apart) within the diverse-biota grainstone facies. The depositional profile, facies zonation and biotic constituents all indicate that the Latemar buildup had a shallow water reef margin, in contrast to previous interpretations that these were upper slope reefs. The syndepositional biotic crusts and inorganic cementation played key roles in stabilizing the boundstone fabric to form a wave-resistant reef fabric.     

Microbial mounds prior to the Frasnian‐Famennian mass extinctions,Hantang, Guilin,South China

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.     

The ecology of Lower Cambrian buildups from Zuune Arts, Mongolia: implications for early metazoan reef evolution

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.     

Coral-stromatolite reef framework, Upper Miocene, Almería, Spain

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.     

Calcimicrobes and microbialites in lagoonal sediments from Mississippian Midale Beds,Williston Basin,southeastern Saskatchewan,Canada

Carbonates of Mississippian age (Viséan) in the Midale Beds, Charles Formation of southeastern Saskatchewan, Canada, produce significant amounts of hydrocarbons. The Midale Beds represent deposition in a shallow-water, periodically restricted, epeiric setting. The sedimentation is characterized by a variety of shallow-water carbonate lithologies ranging from wackestone, packstone, grainstone, to microbial boundstone. Algae, calcimicrobes, and related microbial fabrics are common features in these limestones. Cores and thin sections through the Midale Beds in the Glen Ewen and Midale pools of southeastern Saskatchewan were examined in order to study the contribution of calcimicrobes and microbial fabrics to the sedimentation of Mississippian carbonate rocks in southeastern Saskatchewan. Calcimicrobes and microbial fabrics are the important components in the grainstones and microbial boundstone. The calcimicrobes are commonly found as porostromate forms, including Garwoodia sp. and Ortonella sp., and other forms such as Archaeolithoporella-like, Girvanella-like, Wetheredella-like, and problematic microbes also occur but are not common. Microbial fabrics are characterized by microstromatolites, microbial laminations, thrombolite, clotted peloids, and fenestrate forms. Calcimicrobes stabilized grains and modified and created sediments, and the related syndepositional microbial fabrics affected the development of porosity/permeability of Midale carbonates. Calcimicrobes and microbial fabrics in Midale Beds highlighted a significant account of microbial facies associated with the Mississippian carbonates worldwide.     

Facies, geometry and geological significance of Late Ordovician (early Caradocian) coral bioherms: Lourdes Formation, western Newfoundland

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.     

Platform and off-platform carbonates of the Upper Cambrian of western Maryland, U.S.A.

Upper Cambrian carbonates in western Maryland are comprised of platform facies (Conococheague Limestone) west of South Mountain and basin facies (Frederick Limestone) east of South Mountain. Conocheague platform carbonates contain interbedded non-cyclic and cyclic facies. Non-cyclic facies consist of cross-stratified grainstones, thrombolitic bioherms, and graded, thin-bedded dolostones. These were deposited in shallow, subtidal shelf lagoons. Cyclic facies are composed of repeated sequences of cross-stratified grainstone; ribbon-rock; wavy, prism-cracked laminite; and planar laminated dolostone. The cyclic facies are shallowing-upward cycles produced by lateral progradation of tidal flats over shallow, nearshore subtidal environments. Cyclic and non-cyclic facies are interbedded in the Conococheague in a layer cake fashion, but no higher-order cyclicity can be found. The Frederick Limestone is dominated by monotonously thick sequences of graded, thin-bedded limestones, interbedded with massive peloidal grainstones and beds of breccia up to 10 m thick in the lower Frederick. The breccias contain transported megaclasts of Epiphyton-Girvanella boundstones. The basal Frederick was deposited in a slope-to-basinal setting east of a rimmed shelf. An Epiphyton-Girvanella marginal reef along the shelf edge was the source of the blocks in the breccias. The upper Frederick Limestone formed on a carbonate ramp.     

Lower Cambrian shelf and shelf margin buildups,Flinders Ranges,South Australia1

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.     

黔南晚石炭世礁相地层中造礁生物Tubiphytes研究

广泛分布在黔南晚石炭世礁相地层中,具有多样的生物形态。其造礁作用以粘结方式为主,可以集中密集形成粘结岩礁块,也可以与其它造礁生物共同建造礁体。其建造的礁体分布局限,礁体一般规模不大。Tubiphytes在工作区除形成礁体外,还通过包覆其它生物碎屑和粘连灰泥和碎屑颗粒形成粘结岩,构成珊瑚礁体的基底,起到固结基底的作用;也可以在其它礁体内部粘结充填在礁骨架中的灰泥和碎屑颗粒形成块状粘结岩,起到加固礁体的作用。Tubiphytes与其它生物碎屑一起作为碳酸盐岩造岩的重要组成部分,在礁相地层中也广泛存在。Tubiphytes在黔南晚石炭世礁相地层中是一类具有特色的生物。     

西沙海域西琛1井生物礁性质及储层岩石学特征

西沙海域西琛1井生物礁主要是由红藻门壳状珊瑚藻、有节珊瑚藻和绿藻门仙掌藻等钙藻组成的植物礁,其次为珊瑚礁。礁相类型主要有礁核相和礁后泻湖相。岩石矿物成分单一,以碳酸盐矿物为主,包括低镁方解石和铁白云石;结构组分有生物骨架、粒屑、泥晶和亮晶;结构类型有生物格架结构、生物障积结构、生物节片结构、生物捆扎结构和生物粘结结构。岩石类型包括骨架石灰岩/白云岩、粘结石灰岩/白云岩、粒屑石灰岩/白云岩。储集空间类型有粒间孔、生物体腔孔和藻架孔等原生孔隙和铸模孔、裂缝、颗粒内溶蚀孔、藻类溶孔和扩大的粒间溶孔等次生孔隙。孔隙组合类型以粒间孔＋溶孔＋晶间孔最为发育,储集性能较好。     

广西上泥盆统肾形藻和肾形藻泥丘的发现及其环境意义

引言肾形藻(Renalcis)是A.G.Vologdin发现并命名的一种钙质微体化石,在广义上归属于蓝绿藻(Pratt,1984)。肾形藻通常发育在寒武纪、早奥陶世、泥盆纪和早石炭世的碳酸盐岩地层中。就其形态来说,在漫长的地质年代中没有什么变化,不同形态的肾形藻可出现在不同时代的地层中,各种类型的肾形藻又可共生一处,因此常被认为没有什么时代意义。尽管如此,肾形藻的生长常局限于比较窄的生态和环境范围,又在某些建隆,特别在泥丘中是主要的骨架构筑成分,因而对于沉积微相的研究和细分具有重要的意义。     

塔里木盆地下寒武统微生物礁储集性研究及油气勘探意义

通过塔北西部-柯坪地区大量的野外露头观测及室内薄片观察与物性分析,对塔里木盆地下寒武统肖尔布拉克组上二亚段微生物礁白云岩储集性进行了精细研究。该层微生物礁仅在研究区南部三个剖面有发现,其中在昆盖阔坦剖面发育数量最多、体积最大,呈近东西向带状、串珠状分布;英尔苏和苏盖特布拉克两剖面发育数量和体积皆较小,呈现由南到北逐减趋势。微生物礁白云岩具有粒内孔、晶间孔、溶孔、格架孔、微裂缝和缝合线6种储集空间,但储集性能远低于预期目标,平均孔隙度与渗透率分别仅有1.84%和0.91×10-3 μm2,属于特低孔特低渗储集体。结合前人工作不难发现,塔里木盆地下寒武统甚至更老地层的微生物礁不应再作为台缘带油气勘探的重点对象,而台缘微生物颗粒滩更具有勘探潜力。     

Stromatoporoid growth forms and Devonian reef fabrics in the Upper Devonian Alexandra Reef System,Canada – Insight on the challenges of applying Devonian reef facies models

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.     

柴北缘塔塔楞环斑花岗岩的岩相学和地球化学特征

塔塔楞环斑花岗岩是柴达木盆地北缘一个古生代复式岩体。该环斑花岗岩在主量元素上, 具有富SiO2、K2O和FeO*, 高K2O/Na2O和FeO*/MgO的特点, 其平均值分别为72.86％、5.17％和3.35％,2.22和10.73;∑REE在279.1×10－6～300.3×10－之间,（La/Lu）N为11.32～13.14,δEu在0.28～0.38之间;Ba、Rb、Pb、Th等元素的含量高,而Sr、Cr、Ni、V等元素的含量低。与经典环斑花岗岩相比,二者在岩相学上相同,在地球化学上也有相似之处,即该岩体也表现为高钾、富铁和LREE,Eu亏损的特征,但部分微量元素与典型环斑花岗岩有一定差异。岩体的形成时代和区域构造背景的综合分析显示,该岩体可能是早古生代后碰撞或后造山伸展构造环境下的产物。