Ramp morphology controlling the facies differentiation of a Late Ordovician reef complex at Bachu,Tarim Block,NW China

A carbonate ramp in the shallow‐marine northwestern part of the Central Tarim Uplift, Bachu, NW China, exhibits an extraordinary Late Ordovician reef complex along the Lianglitag Mountains, exposed for a distance of about 25 km. Seven localities within the ‘Middle Red Limestone’ of the Upper Member of the Lianglitag Formation (Katian, Late Ordovician) illustrated the changes in biofacies and lithofacies: northern, seaward‐directed patch reefs are replaced towards the south by coeval grain banks. The patch reef units are dominated by microbial and calcareous algal components. The reefs at the northernmost locality are knoll‐shaped, kalyptra‐shaped or irregularly shaped with sizes of individual reefs increasing from about 2 m in height and diameter. Stratigraphically upward, reefs notably expand to larger structures by several mounds coalescing; they are generally about 10 m thick and tens of metres in lateral extent. The maximum thickness of the main patch reef is more than 30 m, and its diameter is around 100 m. The reefal units turn into biostromes with gentler relief southward and still further south grade into banks composed of peloids and coated grains. The southernmost locality is still a shallow‐water bank, and the coastline is not documented in the study area. The present evidence indicates that the Late Ordovician palaeo‐oceanography provided a number of environments for the optimal growth of carbonate build‐ups; microbial‐calcareous algal communities could thrive in areas where the innovative metazoan reef frameworks consisting of corals and stromatoporoids did not play a significant role. The ramp morphology, especially changes in water depth, controlled the configuration of the reef complex.     

Early Ordovician reefs in South China (Chenjiahe section, Hubei Province): deciphering the early evolution of skeletal-dominated reefs

The Lower Ordovician (late Tremadocian–early Floian) Fenhsiang and the overlying Hunghuayuan Formations at the Chenjiahe section in the Three Gorges area of Hubei Province, South China, include four types of reef: microbe-dominated (lithistid sponge–stromatolite and lithistid sponge–calcimicrobial) reefs, and skeletal-dominated (lithistid sponge–bryozoan and bryozoan–pelmatozoan) reefs. The microbe-dominated reefs are characterized by the dominance of microbial sediments that encrusted and bound the surfaces of sponges to reinforce the reef frameworks. In contrast, the skeletal-dominated reefs are distinguished by bryozoans that encrusted frame-building sponges and pelmatozoans, and that grew downward to fill the open spaces available within the frameworks. A series of these reefs shows a temporal succession in reef type, with a decline in the lithistid sponge–stromatolite reefs and an increase in the lithistid sponges and receptaculitids within the lithistid sponge–calcimicrobial reefs in the Hunghuayuan Formation; the lithistid sponge–bryozoan reefs are common in both the Fenhsiang and Hunghuayuan Formations. These features of the Chenjiahe reefs are in marked contrast to other coeval reefs on the Yangtze Platform and elsewhere. Skeletal-dominated reefs first developed in the Three Gorges and adjacent areas, located on the central part of the platform. Likewise, lithistid sponges and receptaculitids first developed in the Three Gorges area and then expanded their range. In contrast, stromatolites declined over time, but remained abundant on a marginal part of the platform. The spatial–temporal distributions of these reefs on the Yangtze Platform reflect the initiation of the Great Ordovician Biodiversification Event and its consequences, although influenced by local environmental conditions. The Three Gorges area was a center for the development of skeletal-dominated reefs, which were established earlier here than elsewhere in the world. These reef types and their spatial–temporal successions provide invaluable clues to the earliest evolution of skeletal-dominated reefs and their ensuing development during the Middle–Late Ordovician.     

The oldest bryozoan reefs: a unique Early Ordovician skeletal framework construction

Adachi, N., Ezaki, Y. & Liu, J. 2011: The oldest bryozoan reefs: a unique Early Ordovician skeletal framework construction. Lethaia, Vol. 45, pp. 14–23. The oldest bryozoan reefs occur in the Lower Ordovician (late Tremadocian) Fenhsiang Formation of the Three Gorges area, South China. These reefs show a unique type of bryozoan (Nekhorosheviella) framework, and were constructed as follows: the first stage involved colonization by lithistid sponges, which acted as a baffler to trap sediments, providing bryozoans with a stable substrate for attachment. The bryozoans then grew as an encruser on the surfaces of sponges, showing a preferential downwards and lateral growth within the sponge scaffolding to avoid biological and physical disturbance. Finally, these biotic combinations among skeletal organisms formed a rigid, three‐dimensional skeletal framework. This mode of bryozoan growth in association with lithistid sponges is remarkable and unique in its growth direction, and the appearance of such reefs, just prior to the widespread development of skeletal‐dominated reefs as part of the Great Ordovician Biodiversification Event, provides an excellent example of the earliest attempts by skeletal organisms to form frameworks by themselves. This find significantly enhances our understanding of the initial stages of skeletal‐dominated reef evolution and the ensuing development of reefs during the Middle–Late Ordovician. □Bryozoa, Early Ordovician, lithistid sponge, Ordovician radiation, reef.     

The origin of Jurassic reefs: Current research developments and results

Summary In order to elucidate the control of local, regional and global factors on occurrence, distribution and character of Jurassic reefs, reefal settings of Mid and Late Jurassic age from southwestern Germany, Iberia and Romania were compared in terms of their sedimentological (including diagenetic), palaeoecological, architectural, stratigraphic and sequential aspects. Upper Jurassic reefs of southern Germany are dominated by siliceous sponge—microbial crust automicritic to allomicritic mounds. During the Oxfordian these form small to large buildups, whereas during the Kimmeridgian they more frequently are but marginal parts of large grain-dominated massive buildups. Diagenesis of sponge facies is largely governed by the original composition and fabric of sediments. The latest Kimmeridgian and Tithonian spongiolite development is locally accompanied by coral facies, forming large reefs on spongiolitic topographic elevations or, more frequently, small meadows and patch reefs within bioclastic to oolitic shoal and apron sediments. New biostratigraphic results indicate a narrower time gap between Swabian and Franconian coral development than previously thought. Palynostratigraphy and mineralostratigraphy partly allow good stratigraphic resolution also in spongiolitic buildups, and even in dolomitised massive limestones. Spongiolite development of the Bajocian and Oxfordian of eastern Spain shares many similarities. They are both dominated by extensive biostromal development which is related to hardground formation during flooding events. The Upper Jurassic siliceous sponge facies from Portugal is more localised, though more differentiated, comprising biostromal, mudmound and sponge-thrombolite as well as frequent mixed coral-sponge facies. The Iberian Upper Jurassic coral facies includes a great variety of coral reef and platform types, a pattern which together with the analysis of coral associations reflects the great variability of reefal environments. Microbial reefs ranging from coralrich to siliceous sponge-bearing to pure thrombolites frequently developed at different water depths. Reef corals even thrived within terrigeneous settings. In eastern Romania, small coral reefs of various types as well as larger siliceous sponge-microbial crust mounds grew contemporaneously during the Oxfordian, occupying different bathymetric positions on a homoclinal ramp. Application of sequence stratigraphic concepts demonstrates that onset or, in other cases, maximum development of reef growth is related to sea level rise (transgressions and early highstand) which caused a reduction in allochthonous sedimentation. The connection of reef development with low background sedimentation is corroborated by the richness of reefs in encrusting organisms, borers and microbial crusts. Microbial crusts and other automicrites can largely contribute to the formation of reef rock during allosedimentary hiatuses. However, many reefs could cope with variable, though reduced, rates of background sedimentation. This is reflected by differences in faunal diversities and the partial dominance of morphologically adapted forms. Besides corals, some sponges and associated brachiopods show distinct morphologies reflecting sedimentation rate and substrate consistency. Bathymetry is another important factor in the determination of reefal composition. Not only a generally deeper position of siliceous sponge facies relative to coral facies, but also further bathymetric differentiation within both facies groups is reflected by changes in the composition, diversity and, partly, morphology of sponges, corals, cementing bivalves and microencrusters. Criteria such as authigenic glauconite, dysaerobic epibentic bivalves,Chondrites burrows or framboidal pyrite in the surrounding sediments of many Upper Jurassic thrombolitic buildups suggest that oxygen depletion excluded higher reefal metazoans in many of these reefs. Their position within shallowing-upwards successions and associated fauna from aerated settings show that thrombolitic reefs occurred over a broad bathymetric area, from moderately shallow to deep water. Increases in the alkalinity of sea water possibly enhanced calcification. Reefs were much more common during the Late Jurassic than during the older parts of this period. Particularly the differences between the Mid and Late Jurassic frequencies of reefs can be largely explained by a wider availability of suitable reef habitats provided by the general sea level rise, rather than by an evolutionary radiation of reef biota. The scarcity of siliceous sponge reefs on the tectonically more active southern Tethyan margin as well as in the Lusitanian Basin of west-central Portugal reflects the scarcity of suitable mid to outer ramp niches. Coral reefs occurred in a larger variety of structural settings. Upper Jurassic coral reefs partly grew in high latitudinal areas suggesting an equilibrated climate. This appears to be an effect of the buffering capacity of high sea level. These feedback effects of high sea level also may have reduced oceanic circulation particularly during flooding events of third and higher order, which gave rise to the development of black shales and dysaerobic thrombolite reefs. Hence, the interplay of local, regional and global factors caused Jurassic reefs to be more differentiated than modern ones, including near-actualistic coral reefs as well as non-actualistic sponge and microbial reefs.     

Discovery of Anticostia uniformis from the Xiazhen Formation at Zhuzhai,South China and its stratigraphic implication

The Xiazhen Formation is an Upper Ordovician lithostratigraphic unit in the Jiangshan-Changshan-Yushan (JCY) area, which contains series of Late Ordovician reef successions. The reef successions of the Xiazhen Formation at Zhuzhai are critical for evaluation of the Late Ordovician marine diversity and palaeoecology. However, their age has long been uncertain and generally is regarded as of upper Katian, based on the occurrences of shelly fossils and correlation with the stratigraphic equivalent Changwu Formation. The newly discovered graptolite species Anticostia uniformis, in the Xiazhen Formation, together with the combined evidence of brachiopods and sedimentology, indicates an age range for the graptolite locality from the Dicellograptus complanatus Biozone to the Diceratograptus mirus Subzone of late Katian, but the graptolites do not rule out the possibility that it is Hirnantian.     

Lower Devonian reef structures in Russia: an example from the Urals

The Lower Devonian reefs of the Urals were formed in two different environmental settings: (1) the Novaya Zemlya-West-Uralian reefs were rigid organic structures that grew at a passive platform at the eastern margin of Baltica; (2) reefal limestones from the Eastern Urals developed in an island arc during a phase of volcanism. The reef belts can be traced for more than 2,500 km. The largest barrier reefs (up to 1,500 m thick) formed during the Pragian-Lower Emsian (West-Urals zone) and Emsian (East-Urals zone). They are characterized by rather uniform faunal and sedimentary features from the Arctic Ocean as south as near the Aral Lake. The Uralian reef facies was constructed mainly with algal and microbial communities (calcimicrobes and cyanobacteria) in association with low-diverse metazoan assemblages. In the Lower Devonian reefs of both regions, there are similar groups of organisms comprising some of the major taxa of reef-builders and reef-dwellers. The distinctive feature of the Lower Devonian reefs of both regions is the stromatolite-like framework structure. A clear palaeobiogeographic link is obvious between West-Uralian and East-Uralian environment settings during the Early Devonian.     

Age,facies, and geometry of the Sandbian/Katian (Upper Ordovician) pelmatozoan-bryozoan-receptaculitid reefs of the Vasalemma Formation,northern Estonia

The Vasalemma Formation (early Katian, Late Ordovician) of northern Estonia consists of a succession of biodetrital grainstones up to 15 m thick with numerous intercalated reef bodies, which reach diameters of more than 50 m. Four dominant facies types are distinguished within the reef core limestones: (1) a bryozoan framestone—bindstone, (2) an echinoderm bindstone, (3) a receptaculitid-bryozoan-microbial framestone, and (4) a tabulate bafflestone. A linking theme between the different reef-core limestones is the presence of clotted microbial bindstone, which in some places contains spicules. Except for the tabulate bafflestone, all facies types occur in the youngest and oldest intervals of reef growth. Generally, a tendency can be observed with a dominance of echinoderm framestone low in the formation and at the base of individual reefs, towards a more receptaculitid dominated facies at the top of the formation. The reefs developed in a narrow, ca. 20-km-long and max. 5-km-wide band on a shallow NE–SW-directed platform in the central part of the North Estonian Confacies Belt. Reef growth can be constrained toward the latest Keila age, representing the rising limb and the peak interval of the Guttenberg Isotopic Carbon Excursion (GICE). Reef termination falls within a second-order sea-level lowstand, the Frognerkilen Lowstand Event, which led to partial subaerial exposure of the reefs. The dead reefs subsequently and rapidly drowned during the Nakkholm Drowning Event at the Oandu/Rakvere Stage. This timing is nearly equivalent to a phase of enhanced reef development elsewhere in Baltica and probably is related to locally increased nutrient availability during the GICE interval.     

Early ordovician reefs from Argentina: Stromatoporoid vs stromatolite origin

Summary Late Arenigian biohermal reef mounds and biostromes within the shallow-marine platform facies of the upper San Juan Formation of the Precordillera (Western Argentina) represent a new Early Ordovician reef type. The meter-sized reefs are dominated byZondarella communis n.g. n. sp. The new taxon is characterized by domical, bulbous and laminar morphotypes exhibiting growth layers and thin horizontal and vertical as well as intermingled skeletal elements included within different sets. The fossil maybe compared with stromatolites and stromatoporoids but an interpretation as primitive stromatoporoids is favoured.     

Plaeocene reef sediments from the maiella carbonate platform,Italy

Summary Upper Cretaceous and Paleocene reef limestones from the Maiella carbonate platform show how reefs evolved during a time of faunal turn-over. Biostratigraphy and facies analysis of the reef limestones reveal the details of reef growth, composition, and age. Rudists disappeared as reef builders from the Maiella platform shortly before the Cretaceous/Tertiary boundary. Small coral-algal reefs became established in the Danian to Late Thanetian. These scleractinian-red algal dominated boundstones and framestones represent two periods of reef sedimentation and the subsequent interruption of reef growth by emersion and erosion, controlled primarily by fluctuations of relative sea-level. The coral-algal reefs evolved as the taxonomic composition of reef organisms changed. The Paleocene reef sediments are preserved as large slide blocks and as boulders redeposited from the shallow-water platform onto the slope during the course of the Paleocene.     

Reef reconstruction after extinction events of the latest ordovician in the Yangtze platform,South China

Summary Early Silurian reef reconstruction on the Yangtze Platform, in the northern part of the South China Block, is preceded by a combination of regional and global processes. During most of Ashgill time (Late Ordovician), the area was dominated by Wufeng Formation deep water graptolitic black shales. Reefs largely disappeard in the middle of the Ashgill Stage, from the northwestern margin of Cathaysian Land (southeastern South China Block), in advance of the Late Ordovician glaciation and mass extinction, due to regional sea-level changes and regional uplift, unrelated to the mass extinction itselt. Late Ordovician microbial mudmound occurrence is also found in the western margin of the Yangtze Platform, its age corresponding to theDicellograptus complexus graptolite biozone of pre-extinction time. On the Yangtze Platform, a thin, non-reef-bearing carbonate, the Kuanyinchiao Formation (=Nancheng Formation in some sites), thickness generally no more than 1m, occurs near several landmasses as a result of Hirnantian regression. Reappearance of the earliest Silurian carbonates consisting of rare skeletal lenses in the upper part of Lungmachi Formation, are correlated to theacensus graptolite biozone, early Rhuddanian of Shiqian, northeastern Guizhou, near Qianzhong Land. Carbonate sediments gradually developed into beds rich in brachiopods and crinoids in the lower part of Xiangshuyuan Formation, middle Rhuddanian. In the middle part of Xiangshuyan Formation, biostromes, containing abundant and high diversity benthic faunas such as corals, crinoids and brachiopods, show beginnings of reconstruction of reef facies. Substantial reef recovery occurred in the upper part of Xiangshuyuan Formation, lower Aeronian, as small patch reefs and biostromes. During the late Aeronian, carbonate sediments, especially reefs and reef-related facies, expanded on the upper Yangtze Platform, and radiation of reefs occurred in Ningqiang Formation, upper Telychian. The long period of reef recovery, taking several million years, remains difficult to explain, because redistribution of any refugia faunas would be expected to take place soon after the extinction. Reefs and reef-related facies subsequently declined after Telychian time due to regional uplift of the major portion of the Yangtze Platform. Carbonate facies are therefore uncommon in South China during the rest of Silurian time.     

江西玉山上奥陶统凯迪阶三衢山组的丛花海绵(Corymbospongia)*

串管海绵在中–晚奥陶世经历了的首次辐射演化事件, 在北美、新南威尔士、哈萨克斯坦、西伯利亚和中国西北等地的上奥陶统地层中皆有报道, 但研究程度较低。本文系华南奥陶系串管海绵首次系统古生物学的报道, 详细描述江西玉山上奥陶统凯迪阶三衢山组的Corymbospongia (丛花海绵属)化石, 并基于C. amplia Rigby, Karl, Blodgett & Baichtal, 2005和C. mica Rigby & Potter, 1986的标本展示该属化石外壁的微孔等特征性结构, 这2个种具有跨板块的生物地理分布。综合串管海绵产出层的碳酸盐岩微相以及伴生钙藻和珊瑚化石等群落分子的指相参照, 识别C. amplia和C. mica均具有明显的生态专属性: C. amplia为造礁生物, 在小型微生物岩中出现; C. mica则代表适应于更浅水生境的平地群落代表。本研究将为从底栖生物群落角度开展扬子区生物地层学及古地理重建提供进一步的依据。     

鄂尔多斯盆地南缘上奥陶统生物礁的层孔虫化石

文中系统描述了鄂尔多斯盆地南缘淳化县铁瓦殿、岐山县烂泥沟上奥陶统生物礁中的层孔虫化石,包括2目5属9种,分别为囊层孔虫(Cystistroma)、拉贝希层孔虫(Labechia)、穿孔层孔虫(Forolinia)、网格层孔虫(Clathrod ict yon)和蜂巢层孔虫(Ecclimadictyon).建立拉贝希层孔...     

Late Ordovician–Early Silurian facies development and environmental changes in the Subpolar Urals

The continuous Upper Ashgill–Sheinwoodian carbonate succession in the most eastern Kozhym River area in the Subpolar Urals comprises the Yaptikshor (Rawtheyan), Kamennaya baba (Hirnantian), Ruchej and Manyuku (Llandovery–?Sheinwoodian) formations. The facies of the deep subtidal Yaptikshor Fm. mark an abrupt sea‐level rise following emergence of the Bad’ya reef (Rawtheyan). Carbonate breccias at the base of the Kamennaya baba Fm. correlate with the beginning of the Hirnantian glaciation and change upwards towards the Ordovician–Silurian boundary with the development of light‐grey massive boundstone/packstone shoal deposits. An abrupt change in facies to the Rhuddanian–Aeronian Ruchej Fm. continental slope environment marked the start of a long‐term sea‐level rise. The uppermost Aeronian–?Sheinwoodian is represented by submarine canyon carbonate conglobreccias of the Manyuku Fm. unconformably underlying the Balban’yu reef. The rapid facies changes at the base of the Hirnantian and at the Ordovician–Silurian boundary were of global eustatic origin. In contrast, the abrupt changes in the Rawtheyan and the formation of the Manyuku Fm. conglobreccias were of local or regional origin associated with tectonics. They were followed by the start of a regional transgression (Yaptikshor Fm.) and a global transgression marked by the initiation of the Balban’yu Reef in the Sheinwoodian.     

A WESTWARD EXTENSION OF THE UPPER ASHGILLIAN HIRNANTIA FAUNA

The very distinctive Hirnantia fauna of uppermost Ordovician age is here recorded from Ireland, where it is found in association with the upper parts of the Chair of Kildare reef limestone. The most important hrachiopod members of the Hirnantia assemblage are Cliftoma, Cryptothyrella, Plectothyrella, Hirnantia, Eostropheodonta , and Dalmanella which are illustrated and their occurrences at other European localities indicated and discussed, particularly with respect to their differing abundances. The nature of the fauna, in conjunction with some lithological pointers, indicates a shallow water lagoonal environment of deposition. With respect to the Kildare succession, the presence of the Hirnantia fauna indicates that the upper part of the Kildare limestone at least belongs to Zone 8 of the Ashgillian; and it is believed that the North of England Keisley Limestone is also of this age, rather than of Lower or Middle Ashgillian age.     

Biotic structure and morphology of patch reefs from South China (Ningqiang Formation, Telychian, Llandovery, Silurian)

Summary Ningqiang Formation (late Telychian, Llandovery, Silurian), characterized by nearly 3000 m of shales in tercalated with carbonates, is situated between Ningqiang (S. Shaanxi Province) to Guangyuan (N. Sichuan Province) adjacent to the northwest margin of the Yangtze Platform. The high diversity “Xiushan Fauna”, and abundant reef development, illustrate a relatively warm and persistent shallo marine environment in these early Silurian sediments. The sequence shows reef radiation after recovery from the end Ordovician mass extinction envents. Multiple horizons of reef-building occurred within a relatively short geological interval and resulted in more than 30patch reefs up to 200 m in diameter and 1–50 m vertically, composed of abundant fossils. Reef biota include frame-building corals, stromatoporoids, bryozoans, and microbialites, and reef-associated oranisms such as crinoids, brachiopods, trilobites, gastropods, nautiloids and ostracods. Three reefrelated biotic associations are recognised: a) reefs dominated by framework with crinoids and microbia; b) reefs dominated by only crinoids and microbia; and c) crinoiddomainated facies. Seven representative reef examples illustrate different morphologies and growth styles. A high terrigenous debris input and shallow epicontinental ramp, which lacked obvious topographic variation, were major controls which resulted in rather simple reefs; sedimentation was apparently the main constraint on lateral and vertical extension of reefs, and prevented large-scale reef complexes developing.     

A modern-type Kimmeridgian reef (Ota Limestone,Portugal): Implications for Jurassic reef models

Upper Jurassic reefs rich in microbial crusts generally appear in deeper (sponge—‘algal’ crust reefs) or in very shallow but protected settings (coral or coral-coralline sponge meadows with ‘algal’ crusts). Upper Jurassic high-energy reefs (coral reefs and coral-stromatoporoid reefs) normally lack major participation of microbial crusts but rather represent huge bioclastic piles with only minor framestone patches preserved. An exception to this rule is represented by the high-energy, coral-‘algal’ Ota Reef from the Kimmeridgian of the Lusitanian Basin (Portugal). The narrow Ota Reef tract rims a small intra-basinal carbonate platform exhibiting perfect facies zonation (from W to E: Reef tract, back reef sands, peritidal belt, low-energy shallow lagoon). The reef is dominated by massive corals (Thamnasteria, Microsolena, Stylina). Complete preservation of coral framework is rare: like other Upper Jurassic high-energy reefs, the Ota Reef is very rich in debris; however, this debris is largely stabilized by algal and microbial crusts, what contrasts the other examples and gives the Ota Reef the appearance of a typical modern high-energy coral-melobesioid algal reef. Further similarities to modern reefs are the likely existence of a spur-and-groove system, the perfect sheltering of inner platform areas and the occurrence of small islands, as indicated by local blackenings and early vadose and karstic features.     

塔中16井区晚奥陶世良里塔格组的沉积相

塔里木板块中央隆起区的塔中低隆带上奥陶统凯迪阶良里塔格组礁相群落是晚奥陶世生物礁演化阶段的例证。该组分为5个岩性段。塔中16井区位于塔中Ⅰ号断裂坡折带向台地内部延伸的缓坡区,海水深度和水流能量显著控制碳酸盐岩的岩相分布。良里塔格组所赋存的典型动物格架礁集中于台地边缘的高能区,而塔中16井区不属于大型动物格架礁建造的富集区域,其早期多以低能带沉积为主,特别是塔中16井和塔中166井灰泥坪常见;晚期常见高能滩相和灰泥丘以及近礁沉积,可划归为台缘坡折带大型格架礁建造向台内的延伸区,这里的水深和能量变化更频繁。偏西北的井在良二段沉积之后抬升较早,东南的塔中161井则保存部分良一段沉积。     

Triassic reefs in Slovenia

The paper deals with the distribution, paleogeography, age and biota of Triassic reefs in Slovenia. Most of these reefs have not been studied in detail up to now, but the paleographical distributional pattern can be outlined (Figs. 1 and 2). Triassic reefs are known from Central and Northern Slovenia, predominantly occurring at the margins of the “Slovenian trough” (which separates the northern Julian Platform and the southern Dinaric Platform) and at the margins of an intraplatform trough within the Julian platform. Reef growth started in the Ladinian and Cordevolian and continued (with interruptions during the Upper Carnian ?) to the Norian and Rhaetian. Anisian environments are characterized by the predominance of algal mats and dasycladacean algae. Cordevolian patch reefs as well as Norian and Rhaetian reefs were built during the Late Triassic by calcareous sponges and corals, which belong to different species (Tab. 1 and 2). Some smaller Cordevolian patch reefs may have been formed within deeper-water sediments. An interesting facies sequence is developed in the Norian Dachstein Limestone reef of Pokljuka (Julian Alps), starting with deeper-marine cherty limestones, which gradually succeeded by crinoidal limestones followed by reef limestones and lagoonal Dachstein Limestones.     

Permian reefs re-examined: extrinsic control mechanisms of gradual and abrupt changes during 40 my of reef evolution

The evolution of Permian reefs is characterized by the following sequence of events: (1) Late Carboniferous–Cisuralian radiation, (2) early Late Cisuralian (Artinskian–Kungurian) turnover, (3) Guadalupian radiation, (4) end-Guadalupian crisis, (5) Lopingian radiation, (6) end-Lopingian crisis at the PTB (Permian–Triassic boundary), and (7) the at least 7 my (million years) metazoan reef gap during the Early Triassic. The early Late Cisuralian turnover and the end-Guadalupian reef crisis are gradual changes, while the end-Lopingian reef crisis represents an abrupt event. Lopingian reefs occur in a zone from 40 °N to 15 °S, Guadalupian reefs in an extended equatorial zone from 35 °N to 35 °S, and Lopingian reefs in a narrow equatorial zone of 20 °N and 20 °S. This pattern resulted from a network of global and regional control mechanisms including the assemblage of Pangea, the northward drift of continents, the opening of Neo-Tethys, and second-order sea level changes. The mechanism of the extinction has been intensely debated and a combination of the above mentioned long-term changes and abrupt ocean anoxia or hypercapnia (CO₂-poisoning) for the end-Guadalupian reef crisis is considered.