Microbial boundstone dominated carbonate slope (Upper Carboniferous,N Spain): Microfacies,lithofacies distribution and stratal geometry

Summary The Carboniferous, particularly during the Serpukhovian and Bashkirian time, was a period of scarce shallow-water calcimicrobial-microbialite reef growth. Organic frameworks developed on high-rising platforms are, however, recorded in the Precaspian Basin subsurface, Kazakhstan, Russia, Japan and Spain and represent uncommon occurrences within the general trend of low accumulation rates and scarcity of shallow-water reefs. Sierra del Cuera (Cantabrian Mountains, N Spain) is a well-exposed high-rising carbonate platform of Late Carboniferous (Bashkirian-Moscovian) age with a microbial boundstone-dominated slope dipping from 20° up to 45°. Kilometer-scale continuous exposures allow the detailed documentation of slope geometry and lithofacies spatial distribution. This study aims to develop a depositional model of steep-margined Late Paleozoic platforms built by microbial carbonates and to contribute to the understanding of the controlling factors on lithofacies characteristics, stacking patterns, accumulation rates and evolution of the depositional architecture of systems, which differ from light-dependent coralgal platform margins. From the platform break to depths of nearly 300 m, the slope is dominated by massive cement-rich boundstone, which accumulated through the biologically induced precipitation of micrite. Boundstone facies (type A) with peloidal carbonate mud, fenestellid and fistuliporid bryozoans, sponge-like molds and primary cavities filled by radiaxial fibrous cement occurs all over the slope but dominates the deeper settings. Type B boundstone consists of globose centimeter-scale laminated accretionary structures, which commonly host botryoidal cement in growth cavities. The laminae nucleate around fenestellid bryozoans, sponges, Renalcis and Girvanella-like filaments. Type B boundstone typically occurs at depths between 20–150 m to locally more than 300 m and forms the bulk of the Bashkirian prograding slope. The uppermost slope boundstone (type C; between 0 and 20–100 m depth) includes peloidal micrite, radiaxial fibrous cement, bryozoans, sponge molds, Donezella, Renalcis, Girvanella, Ortonella, calcareous algae and calcitornellid foraminifers. From depths of 80–200 m to 450 m, 1–30 m thick lenses of crinoidal packstone, spiculitic wackestone, and bryozoan biocementstone with red-stained micrite matrix are episodically intercalated with boundstone and breccias. These layers increase in number from the uppermost Bashkirian to the Moscovian in parallel with the change from a rapidly prograding to an aggrading architecture. The red-stained strata share comparable features with Lower Carboniferous deeper-water mud-mound facies and were deposited during relative rises of sea level and pauses in boundstone production. Rapid relative sea-level rises might have been associated with changes in oceanographic conditions not favourable for thecalcimicrobial boundstone growth, such as upwelling of colder, nutrient-rich waters lifting the thermocline to depths of 80–200 m. Downslope of 150–300 m, boundstones interfinger with layers of matrix-free breccias, lenses of matrix-rich breccias, platform- and slope-derived grainstone and crinoidal packstone. Clast-supported breccias bound by radiaxial cement are produced by rock falls and avalanches coeval to boundstone growth. Matrix-rich breccias are debris flow deposits triggered by the accumulation of red-stained layers. Debris flows develop following the relative sea-level rises, which favour the deposition of micrite-rich lithofacies on the slope rather than being related to relative sea-level falls and subaerial exposures. The steep slope angles are the result of in situ growth and rapid stabilization by marine cement in the uppermost part, passing into a detrital talus, which rests at the angle of repose of noncohesive material. In the Moscovian, the aggradational architecture and steeper clinoforms are the result of increased accommodation space due to tectonic subsidence and due to a reduction of slope accumulation rates (from 240±45−605±35 m/My to 130±5 m/My). The increasing number of red-stained layers and the decrease of boundstone productivity are attributed to environmental changes in the adjacent basin, in particular during relative rises of sea level and to possible cooling due to icehouse conditions. The geometry of the depositional system appears to be controlled by boundstone growth rates. During the Bashkirian, the boundstone growth potential is at least 10 times greater than average values for ancient carbonate systems. The slope progradation rates (nearly 400–1000 m/My) are similar to the highest values deduced for the Holocene Bahamian prograding platform margin. The fundamental differences with modern systems are that progradation of the microbial-boundstone dominated steep slope is primarily controlled by boundstone growth rates rather than by highstand shedding from the platform top and that boundstone growth is largely independent from light and controlled by the physicochemical characteristics of seawater.     

Maastrichtian facies succession and sea-level history of the Hossein-Abad,Neyriz area,Zagros Basin

The Maastrichtian shallow-water carbonate platform (Tarbur Formation) is described from outcrop in southwest Iran. It is characterised by eight microfacies types, which are dominated by larger foraminifera, rudist debris and dasycladacean algae. They are grouped into four distinct depositional settings: tidal flat, lagoon, barrier and open marine. The depositional settings include stromatolitic boundstone of tidal flat, peloidal dasycladacean miliolids wackestone and peloid bioclastic imperforate foraminifera wackestone of restricted lagoon, Omphalocyclus miliolids bioclast packstone–grainstone and miliolids intraclast bioclast packstone–grainstone of open lagoon, rudist bioclast grainstone of inner-platform shoals and rudist bioclast floatstone–rudstone and bioclastic wackestone of open-marine environments.

The facies and faunal characters are typical of a ramp-like open shelf. The lack of reef-constructing organisms resulted in a gently dipping ramp morphology for the margin and slope. On the basis of facies analysis, three depositional sequences (third order) are defined.     

Paleoecology of Pennsylvanian phylloid algal buildups in south Guizhou,China

Pennsylvanian phylloid algal reefs are widespread and well exposed in south Guizhou, China. Here we report on reefs ranging from 2 to 8 m thickness and 30–50 m lateral extension. Algae, the main components, display a wide spectrum of growth forms, but are commonly cyathiform (cup-shaped) and leaf-like (undulate plates). The algal reef facies is dominated by boundstone. Algal thalli form a dense carpet whose framework pores are filled with marine cement and peloidal micrite. The peloidal matrix is dense, partly laminated or clotted with irregular surfaces and often gravity defying. Algal reefs in Guizhou differ from examples reported to date by the high biodiversity of organisms other than phylloids: e.g., the intergrowth of algae with corals (some of which are twice the size of algal thalli) and numerous large brachiopods. This contrasts to previous views that phylloid algal “meadows” dominated the actual seafloor, excluding other biota. Also, the pervasive marine cements (up to 50%) including botryoidal cement are noteworthy. Algal reefs developed at platform margins, a depositional environment similar to that of modern Halimeda mounds in Java, Australia and off Bahamas, and to that of time-equivalent examples reported from the Canadian Arctic Archipelago. Whereas nutrients appear decisive in the growth of Halimeda reefs, algal reefs reported herein seemingly grew under conditions of low nutrient levels. Overall, algal reefs in Guizhou challenge previous views on growth forms, diversity patterns, and depositional environments and add to the spectrum of these partly puzzling biogenic structures.     

Transgressive–regressive sequence stratigraphy of Pennsylvanian Donezella bioherms in a foreland basin (Lena Group, Cantabrian Zone, NW Spain)

A well-preserved Pennsylvanian (early Moscovian) succession including Donezella mounds, which accumulated in a highly subsiding foreland basin (Cantabrian Zone, NW of Spain), is described and discussed. This succession has been interpreted as one 3rd-order sequence reaching a thickness up to 815?m and recording?~2.3-My duration. It consists of four 4th-order transgressive–regressive (T-R) sequences (105–350?m thick and?~0.6-My duration), each subdivided into several 5th-order (~70-ky duration) meter-scale cycles (23-m average thickness). Nearly all the Donezella mounds are present in the second and third 4th-order sequences defined (Levinco Formation). They are up to?~90?m in thickness and several hundreds of meters wide, showing lenticular to domal morphologies with steep slopes up to 35–40°. Bioherms are composed of micritic boundstones with heterogeneous microfabrics and a diverse biotic community, including the microproblematic Donezella, calcitornellid foraminifers, bryozoans, agglutinated worm tubes, crinoids, and calcareous algae (red Komia/Ungdarella, beresellids, dasycladaceans and phylloids). According to the biotic assemblage and sedimentological features, these Donezella-rich bioherms thrived in a relatively shallow and low-energy environment (below fair-weather wave-base), and resulted from the baffling and binding ability of Donezella and associated biota, and the in situ-precipitation of microbial micrite. The upward evolution of the succession mainly resulted from the interplay between high tectonic subsidence rates and high-frequency moderate-amplitude glacioeustatic sea-level changes. The mounds growth mainly occurred during the transgressive phase of the 3rd-order sequence (Vereian), whereas during the regressive phase (Kashirian), deltaic siliciclastics prograding westward gradually buried and prevented the buildup development.     

Mud mounds: A polygenetic spectrum of fine-grained carbonate buildups

Summary This research report contains nine case studies (part II to X) dealing with Palaeozoic and Mesozoic mud mounds, microbial reefs, and modern zones of active micrite production, and two parts (I and XI) summarizing the major questions and results. The formation of different types ofin situ formed micrites (automicrites) in close association with siliceous sponges is documented in Devonian, Carboniferous, Triassic, Jurassic and Cretaceous mounds and suggests a common origin with a modern facies found within reef caves. Processes involved in the formation of autochthonous micrites comprise: (i) calcifying mucus enriched in Asp and Glu, this type presumably is linked to the formation of stromatolites, thrombolites and massive fabrics; (ii) protein-rich substances within confined spaces (e.g. microcavities) result in peloidal pockets, peloidal coatings and peloidal stromatolites, and (iii) decay of sponge soft tissues, presumably enriched with symbiotic bacteria, lead to the micropeloidal preservation of parts of former sponge bodies. As a consequence, there is strong evidence that the primary production of micrite in place represents the initial cause for buildup development. The mode of precipitation corresponds to biologically-induced, matrix-mediated mineralization which results in high-Mg-calcites, isotopically balanced with inorganic cements or equilibrium skeletal carbonates, respectively. If distinct automicritic fabrics are absent, the source or origin of micrite remains questionable. However, the co-occurring identifiable components are inadequate, by quantity and physiology, to explain the enhanced accumulation of fine-grained calcium carbonate. The stromatolite reefs from the Permian Zechstein Basin are regarded as reminiscent of ancestral (Precambrian) reef facies, considered the precursor of automicrite/sponge buildups. Automicrite/sponge buildups represent the basic Phanerozoic reef type. Analogous facies are still present within modern cryptic reef habitats, where the biocalcifying carbonate factory is restricted in space.     

Hydraulic sorting of microbiota in calciturbidites— A dinantian case study from the rheinische schiefergebirge,Germany

Summary A calciturbidite bed from the lower part of the Kieselkalk Formation (late cd II) at Wallau, eastern Rheinisches Schiefergebirge, displays ideal grading of reworked calcareous shallow-water microbiota, ranging from plurimillimetric agglutinated foraminifers and fragments of calcareous algae (Koninckopora sp.) to plurimicronic calcispheres, radiolarians and sponge spicules. Microbiota derived from all levels of the platform. Correspondingly, several carbonate microfacies types could be discerned. The early diagenetic micrite base of the turbidite preserved the anoxic basinal facies. The turbidite bed belongs to Foraminiferal Zone 15 (V3bα), theAlbaillella cartalla Zone (radiolarian chronology), and is the Lower and part of the Uppertexanus Zone (standard conodont zonation). From the few published data on foraminifers, the Kieselkalk is thought to range from Mid Viséan V2b to Late Viséan V3b gamma.     

Pennsylvanian fusulinids and calcareous algae from Sonora (northwestern Mexico), and their biostratigraphic and palaeobiogeographic implications

Pennsylvanian carbonates are widespread in Sonora (Mexico) and contain a diverse biota of foraminifers and calcareous algae. Detailed studies here are devoted to the outcrops of the Sierra Agua Verde and Cerro El Tule. The Late Atokan (early Late Moscovian part), Desmoinesian (= late Late Moscovian) and Missourian (= Kasimovian) stages are especially rich in fusulinids and algae. The principal zones of fusulinids of Wilde encountered are A3, DS1 and MC1–2. New data are given about the genera Fusulinella, Parawedekindellina, Zellerella, Komia and Paraepimastopora, in order to establish migrations or vicariances between Mexico and Palaeotethys.     

Nubecularia-coralline algal-serpulid-microbial bioherms of the Paratethys Sea—Distribution and paleoecological significance (upper Serravallian,upper Sarmatian,Middle Miocene)

Nubecularia bioherms represent unique bioconstructions that are restricted to the upper Serravallian of the Paratethys and have been reported since the 19th century. They occur in the Central Paratethys in the late Sarmatian and the Eastern Paratethys in the Bessarabian both regional stages of the respective Paratethyan areas. In this study, several locations in the Vienna and Styrian basins of the Central Paratethys were studied out of which four localities were documented in detail (Wolfsthal, Maustrenk, St. Margarethen—Zollhaus, Vienna—Ruzickagasse) to reconstruct their sedimentary setting, their internal composition, and their indications of environmental parameters. The detailed studies included logging of outcrop sections, petrographic, facies and biotic analyses of polished slabs and thin sections and also cathodoluminescence analyses. These concluded that these bioconstructions are not only composed of the foraminifer Nubecularia but represent a complex mixture and interrelationships of Nubecularia, serpulids and microbial carbonate. Four boundstone types can be differentiated: Nubecularia boundstone, Nubecularia-coralline algal boundstone, stromatolitic/thrombolitic boundstone and serpulid-nubeculariid-microbial boundstone. The first 3 types are characteristic of specific localities; the fourth type occurs in all studied locations and represents the terminal association on top of the three other types. The three basal boundstones are predominantly of columnar growth form irrespective of dominance of Nubecularia, coralline algae or microbial carbonate, and the terminal boundstone is widely irregularly organized. The general depositional environment is characterized by cross-bedded oolitic grainstones with abundant quartz grains, miliolid foraminifers and mollusks. Intercalated are microbial carbonates mostly stromatolites but also thrombolites. This indicates a general high water energy environment interrupted by more calm periods when the microbial carbonate was built. The 3 basal types of bioconstructions are interpreted to reflect decreasing food supply and/or oxygenation from Nubecularia over Nubecularia-coralline algal to stromatolitic/thrombolitic boundstone. The serpulid-nubeculariid-microbial boundstone reflects an internal succession with a decrease of the same parameters. Water depth is considered very shallow ranging from 0 to a few meters, and salinity was normal marine to hypersaline. The reconstructed paleoenvironment with dominating oolite shoals and seagrass meadows was not restricted to the Central Paratethys but extended over the entire Paratethys and represented the largest oolite facies area of the entire Cenozoic!     

Microbial origin of travertine fabrics—two examples from Southern Germany (Pleistocene stuttgart travertines and miocene riedöschingen Travertine)

Summary In Southern Germany, two examples of travertines of different age and depositional morphology were examined in detail. Travertines are laminated carbonate rocks formed by precipitation from mineral and/or thermal waters. They include characteristic facies types, such as bushy layers (‘shrubs’) referred to calcification of branching microbes (‘Dichothrix’-morphotype), laminar microbial mats, peloidal layers, and gas bubble layers formed within the sediment. In travertines, microbial activity is the most important factor for carbonate precipitation. Tufas differ from travertines by their abundance of molds of higher plants (leaves, reed, moss, green algae). They may be associated with travertines, but do not exhibit strict travertine facies types. Tufas are common in normal fresh water environments. Contrary to travertines and tufas, calcareous sinters usually occur in restricted areas like spring fissures, caves, or in pores, where microbial activity is not totally absent, but not of paramount importance for precipitation. Pedogenetic processes, which can alter travertine deposits, are responsible for large-scale features such as tepee-structures, and some intraclastic layers, and microscopic structures like endolithic borings andMicrocodium. Travertines may also grade into lacustrine limestones with Characeae, ostracods, and aquatic gastropods.     

Microbial contribution to deposition of upper carboniferous and lower Permian seamount-top carbonates,Akiyoshi, Japan

Summary Microbial organisms significantly contributed to the accumulation of shallow-marine carbonates in an open-ocean realm of the Panthalassan Ocean during Late Carboniferous-Early Permian time. The Jigokudai plateau in the northern part of the Akiyoshidai Plateau is the study area, where the limestone of the Upper Carboniferous Kasimovian Stage to the Lower Permian Artinskian Stage is well exposed. The fusulinid biostratigraphy as well as top-bottom geopetal fabrics revealed that the rocks of the study area are overturned. The thickness of this succession is approximated to 150 m. The succession is lithologically divided into the Lower Jigokudai and Upper Jigokudai formations. The lime-stones of these formations were deposited in a lagoonal setting. The Lower Jigokudai formation (95 m thick: Kasimovian to Asselian) is characterized by sand shoal facies represented by crinoid-Tubiphytes-fusulinid peloidal pack/grainstones and oolitic grainstones. Phylloid algal grain/packstones and microbial boundstones subordinately crop out. The Upper Jigokudai Formation (55 m thick: Sakmarian to Artinskian) is characterized by shoal and tidal flat facies represented by mollusk-fusulinid peloidal grain/rudstones, and peloidal grain/rudstones and peloidal lime-mudstones, respectively. Laterally discontinuous microbial bound-stones occur intercalated in mollusk-fusulinid peloidal grain/rudstones. This formation contains pendant and meniscus cements, and flat-pebble breccia indicative of an intertidal deposition and subaerial exposure. Various types of boundstone and organosedimentary structures constructed mainly by filamentous cyanobacteria,Tubiphytes obscurus tubular microproblematicum A, and other microproblematica were recognized. Significant facies types are (1) filamentous cyanobacteria-microproblematicum A bind/framestones, (2)Tubiphytes obscurus bindstones, (3) stromatolitic bindstones, (4) microbial laminites, (5) microbially linked structures, (6) oncoids, (7) microproblematica B-C framestones. The calcimicrobes, combined with synsedimentary cementation, formed small-scale and low-relief mounds of these facies, and greatly contributed to the deposition of the Kasimovian to Artinskian Panthalassan buildup.     

Sedimentary facies and paleoenvironmental interpretation of the Oligocene larger-benthic-foraminifera-dominated Qom Formation in the northeastern margin of the Tethyan Seaway

The well-exposed outcrops of the Bujan, northern Abadeh, and Varkan stratigraphic sections of the Qom Formation in the Iranian part of the “northeastern margin” of the Tethyan Seaway were characterized by abundant biogenic components dominated by foraminifers, coralline red algae, and corals. The Qom Formation is Rupelian–Chattian in age in the study areas. Based on the field investigations, depositional textures, and dominant biogenic components, fifteen (carbonate and terrigenous) facies were identified. These facies can be grouped into four depositional environments: open marine, open lagoon, restricted lagoon, and continental braided streams. The marine facies were deposited on a ramp-type platform. The euphotic inner ramp was characterized mainly by imperforate foraminifera, with co-occurrence of some perforate taxa. These facies passed basinward into a mesophotic (middle) ramp with Neorotalia packstone (F5), coral, coralline algae, perforate foraminiferal packstone (F4), and coral patch reefs (F7). The deeper, oligophotic ramp facies were marly packstones with planktonic and hyaline benthic foraminifera, including large lepidocyclinids and nummulitids. The abundance of perforate foraminifera and the absence of facies indicating restricted lagoonal or intertidal settings suggest that the Varkan section was deposited mainly in open marine settings with normal salinity. The prevalence of larger benthic foraminiferal and red algal assemblages, together with the coral facies, indicates that carbonate production took place in tropical–subtropical waters.     

A late Devonian (Frasnian) coral-bafflestone reef at Houshan in Guilin, South China

Summary Givetian to early Carboniferous sediments of South China are characterized by carbonates. Middle and Late Devonian strata are best developed in the Guilin area. Reefs and organic shoals are recorded by various lithofacies types indicating the existence of an extended carbonate platform and a change of the composition of reef communities in time. Starting in the late Devonian, stromatoporoids and corals were replaced by algae that subsequently played an important role together with stromatoporoids, receptaculitids and fasciculate rugose corals in reef communities. In Houshan, 5 km west of Guilin, a coral-bafflestone reef occurs in the Frasnian strata, situated near an offshore algal-stromatoporoid reef. The coral reef was formed in a back-reef area adjacent to the inner platform margin. The coral-bafflestone reef is unique among the late Devonian reefs of South China with regard to the biotic composition. The reef is composed of fasciculate colonies ofSmithiphyllum guilinense n. sp. embedded within in packstones and wackestones. The height of colonies reaches 1 m. The community is low-diverse. The species ofSmithiphyllum occurring in the Frasnian reef complexes of Guilin exhibit a distinct facies control:Smithiphyllum guilinense occurs in or near to margin facies and formed bafflestone, constituting a coral reef whereasSmithiphyllum occidentale Sorauf, 1972 andSmithiphyllum sp.—characterized by small colonies with thin corallites—are restricted to the back-reef and marginal slope facies. The bush-like coral colonies baffled sediments. Algae and stromatoporoids (mainlyStachyodes) are other reef biota. Reef-dwelling organisms are dominated by brachiopods. The reefs are composed from base to top of five lithofacies types: 1) cryptalgal micrite, 2) peloidal packstone, 3) stromatactis limestone, 4) coral-bafflestone, and 5) pseudopeloidal packstone. The reef complex can be subdivided into back-reef subfacies, reef flat and marginal subfacies, and marginal fore-slope subfacies. The Houshan coral-bafflestone reef is not a barrier reef but a coral patch reef located near the inner margin of a carbonate platform.     

Relationships between foraminiferal assemblages and depositional sequences in Jahrum Formation,Ardal area (Zagros Basin,SW Iran)

The Jahrum Formation was deposited in the foreland basin in southwest Iran (Zagros Basin). The Zagros mountain belt of Iran, a part of the Alpine–Himalayan system, extends from the NW Iranian border through to SW Iran, up to the strait of Hormuz. The various facies of the Jahrum Formation were deposited in four main genetically related depositional environments, including: tidal flat, lagoon, shoal and open marine. These are represented by 14 microfacies. The Jahrum Formation represents sedimentation on a carbonate ramp. Tidal flat facies are represented by fenestral fabric, stromatolitic boundstone and thin-bedded planes. Carbonate deposition in a shallow marine lagoon was characterised by wacke–packstone, dominated by various taxa of imperforate foraminifer. The shoals are made up of medium- to coarse-grained skeletal and peloidal grainstone. This facies was deposited predominantly in an active high energy wave and current regime, and grades basinward into middle ramps facies are represented by wackestones–packstones with a diverse assemblage of echinoderm and large benthic foraminifers with perforate wall. Outer ramp facies consist of alternating marl and limestones rich in pelagic foraminifera. There is no evidence for resedimentation processes in this facies belt. The sequence stratigraphy study has led to recognition of three third-order depositional sequences.     

Coralline red algal limestones of the late Eocene alpine Foreland Basin in Upper Austria: Component analysis, facies and palecology

Summary Late Eocene sediments of the Upper Austrian Alpine Foreland Basin discordantly overlie Mesozoic and crystalline rocks, which are deeply eroded and form a distinct pre-Eocene relief. Late Eocene deposits contain red algal limestones with a remarkable lateral extent and a high diversity of sedimentary facies. Towards the south the algal limestones change into more clastic sediments, which are characterized by larger foraminifera and bryozoans. Main components are coralline algal branches and detritus, coralline crusts, rhodoliths, peyssonneliacean aggregates and crusts, nummulitid and orthophragminid foraminifera, corals, bryozoans, as well as terrigenous components. Rank correlation and factor analysis were calculated in order to obtain informations about relations between components. Hierarchical cluster analysis allowed the designation of 17 facies, most of them are dominated by coralline algae. Actualistic comparisons and correlations obtained from statistical analyses allowed the reconstruction of the depositional environments. Main features of the northern area are huge accumulations of unattached coralline algae (branches, rhodoliths, detritus), which are comparable to the present-day “Maerl”-facies. They formed loose frameworks cut by sand channels. The frequency of coralline detritus decreases upsection. Peyssonneliacean algae in higher parts of the profiles show growth-forms that are comparable to peyssonneliaceans of the Mediterranean circalittoral soft bottoms. This succession can be interpreted by an increasing relative sea level. Besides, crustose coralline algal frameworks were growing on morphological highs which are partially comparable to the present-day “Coralligéne de Plateau” of the Mediterranean Sea. In contrast to the northern area, sedimentation rate of the southern area is too low to keep up with rising sea level. The typical succession from nummulitid- to orthophragminid-and bryozoan-dominated facies can be interpreted by an increasing water depth from shallowest subtidal to the deeper photic zone and finally to the aphotic zone.     

Carboniferous reef succession of the Panthalassan open-ocean setting: example from Omi Limestone, central Japan

Summary The Carboniferous-Permian (Visean-Midian) Omi Limestone in the Akiyoshi Terrane, central Japan is a large carbonate unit developed on a seamount in the Panthalassa Ocean. As the seamount subsided during Carboniferous and Permian time, the carbonate deposition at the top of a seamount was almost continous. Terrigenous siliciclastic sediments are absent, because the seamount was situated in an open-ocean setting. The lower part of this seamount-type limestone records a nearly continuous Carboniferous reef succession. Sedimentary facies in the Carboniferous part of the Omi Limestone are generally highly diverse, but their diversity varies in each age. The Upper Carboniferous part consists of highly diversified facies including fore reef, reef front, reef crest, sand shoal, and lagoon facies, while a simple facies assemblage, composed only of fore reef, reef front, and sand shoal facies, occurs in the Lower Carboniferous. The Carboniferous reef succession consists of four phases characterized, in ascending order, by the coralbryozoan-crinoid community, problematic skeletal organism-microencruster community, chaetetid-microencruster community, and calcareous algal community. The first phase, comprising the coral-bryozoan-crinoid community, occurs in theEndothyra spp. Zone to theEostaffella kanmerai Zone (Visean to Serpukhovian). This community acted only as sediment-bafflers and/or contributors. The second phase, represented by the problematic skeletal organism-microencruster community, is developed in theMillerella sp. Zone to theAkiyoshiella ozawai Zone (Bashkirian to lowermost Moscovian), and the third phase, comprising the chaetetid-microencruster community, occurs in the overlyingFusulinella biconica Zone (Lower Moscovian). These two communities are characterized by highly diversified reef-building organisms that had the ability to build rigid frameworks. Calcareous algae and incertae sedis such asHikorocodium, solenoporaceans and phylloid algae characterize the fourth phase, which occurs in theBeedeina sp. Zone (Upper Moscovian). The changes of the reef communities were sucessive for a long period of more than 40 m.y., and each community was distributed in various environments. In addition, the continuous subsidence of the isolated seamount resulted in environmental stability. These properties indicate that this succession represents the biotic evolution of reef-building organisms. The problematic skeletal organism-microencruster community and chaetetid-microencruster community of the Late Carboniferous formed wave-resistant and rigid frameworks along with abundant submarine cements. The growth of these reef frameworks resulted in the formation of highly diversified sedimentary facies comparable to those of a modern reef complex. Such reefs are also recognized in the seamount-type Akiyoshi Limestone, but rare on Carboniferous Pangean shelves. Therefore, the formation of these types of reefs appear to be characteristic of open-ocean seamount settings, which differed from epicontinental shelf settings in having no siliciclastic input, being exposed to relatively strong openocean waves and swells, and probably more environmental stability resulting from the relatively continuous subsidence of the seamount.     

A close look at late carboniferous algal mounds: Schulterkofel,Carnic Alps,Austria

Summary During the uppermost Carboniferous and lowermost Permian algal mounds were formed in inner shelf settings of the Carnic Alps (Austria/Italy). A specific mound type, characterized by the dominance of the dasyclad green alga Anthracoporella was studied in detail with regard to geometry, relationship between mound and intermound rocks, composition of the sediment, biota and diagenetic criteria. The two meter-sized mounds studied, occur within depositional sequences of transgressive systems tracts in the Lower Pseudoschwagerina Limestones (uppermost Gzhelian) at the flank of the Schulterkofel. The mounds consist of an Anthracoporella core facies with a spongecrust boundstone facies at the base and at the top. The massive limestones of the Anthracoporella core facies exhibit abundant algal tufts and bushes, frequently in life position. The limestones of the intermound facies represented by thin-bedded bioclastic wackestones and packstones with abundant phylloid algae underlie and overlie the mounds. Intercalations of intermound beds within the mound facies indicate sporadic disruption of mound growth. Onlapping of intermound beds on steep mound flanks indicate rapid stabilization and lithification of mound flanks and the existence of a positive paleorelief. Asymmetrical shape of the mounds may be current controlled. Mound and intermound biota differ in the prevailing algae but are relatively similar with regard to associated foraminifera. Conspicuous differences concern bioerosion and biogenic encrustations. Bothare, high in intermound areas but low in the Anthracoporella core facies. The mounds show no ecological zonation. The mounds grew by in-place accumulation of disintegrated algal material and trapped bioclastic material between erect algal thalli. The comparison of the various Anthracoporella mounds demonstrates that almost each mound had ist own history. Establishing a general model for these mounds is a hazardous venture.     

The role of microbes in reef-building communities of the Cannindah limestone (Mississippian), Monto region, Queensland, Australia

Reefs in the Cannindah Limestone at Old Cannindah Homestead, Monto region, Queensland, are exceptional in Eastern Australian Mississippian (Carboniferous) build-ups because of their largest dimension and differentiated microbial fabrics. Calcimicrobes and microbial carbonates, which represent a marine reefal environment occupied by both corals and sponges, are particularly abundant in the reef framework fabrics compared to other Mississippian build-ups in the world. They contributed significantly to the rigidity of the reefs on a crinoidal bank setting. Metazoans and calcimicrobes coexisted and played different roles in reef construction. Reef-building and cavity-dwelling microbes include Renalcis, Palaeomicrocodium, Girvanella, problematic Aphralysia, Ortonella, Shamovella-like, Rothpletzella-like, Wetheredella-like, and some problematic calcimicrobes, which occur in inter-corallite infillings of fasciculate rugose corals, in thrombolitic textures, in or within deposits between microdigitate stromatolite and laminated microbialites, and in reef cavities. Some reef intervals are entirely formed by Renalcis, Palaeomicrocodium, problematic calcimicrobes, and cement. Girvanella, as an encrusting calcimicrobe, generally bound bioclasts and micrite, or together with cement, formed boundstone. Microbial carbonates, including thrombolites, microencrusters, microdigitate stromatolite, laminated and tabular microbialite, irregular layers of self-encrusting vesicles, and microbial micrite, occur commonly in reef framestone and boundstone. The role of microbes and relevant microbial carbonates in the Cannindah reef limestone highlighted a significant account of microbial facies complexes associated with the Mississippian reefs.     

Platform environments, microfacies and systems tracts of the upper Cenomanian-lower Santonian of Sinai, Egypt

Summary Factors controlling grain composition and depositional environments of upper Cenomanian—Santonian limestones of Sinai are discussed. The mainly shallow-water, inner-platform setting investigated is subdivided into five major facies belts, each represented by several microfacies types (MFTs). Their lateral distribution patterns and their composition underline aclear relation between depositional environment and platform position. The facies belts include sandstones and quartzose packstones of siliciclastic shorefaces, mudstones and bioclastic wackestones of restricted lagoons, shallow-subtidal packstones with diverse benthic foraminifera and calcareous algae, bioclastic and/or oolitic grainstones of inner-platform shoals, and wackestones of deep open-marine environments. The microfacies distribution patterns of the Cenomanian-Santonian strata are evaluated with respect to local and regional large-scale environmental changes. While protected shallow-subtidal environments with only subordinate ooids and oncoids prevail during the late Cenomanian, high-energy oolithic shoals and carbonate sands occur locally during the middle and late Turonian. They were probably related to a change of the platform morphology and a reorganisation of the platform after a late Cenomanian drowning. In the Coniacian-Santonian, the lack of ooids, oncoids, and the decrease of calcareous algae versus an increase in siliciclastics indicate a shift to lower water temperature and to a more humid climate. Especially in the Turonian, the interplay between sea-level changes, accommodation, hydrodynamics, and siliciclastic input is reflected by lithofacies and biofacies interrelation-ships that are elaborated within individual systems tracts. In particular, increasing accommodation intensified circulation and wave-agitation and controlled the distribution of high-energy environments of the middle and upper Turonian trans-gressive systems tracts. During highstands protected innerplatform environments prevailed.     

Biotic composition and microfacies distribution of Upper Triassic build-ups: new insights from the Lower Carnian limestone of Lesno Brdo,central Slovenia

The architecture and composition of Middle to lower Upper Triassic platforms is often obscured by dolomitization. Hence, comparatively little is known about their architectures compared to their size and geographic extent. An active quarry near Lesno Brdo (central Slovenia) offers an excellent exposure of Lower Carnian (Julian) massive limestone, which is diagenetically little altered. A detailed microfacies analysis along a 15.5-m log revealed the presence of three facies types: fine-grained limestone as a groundmass, blocks and globular masses of sponge-microbialite boundstone, and lens-like aggregations of polychaete (terebellid) tubes. Sponge-microbialite boundstone contains a rather small number of cosmopolitan sponge taxa, solenoporacean red algae, microproblematica, bryozoans, and a small proportion of dwelling fauna. Instead, stromatolites represent the main constituent. While some blocks appear to have truncated margins, others show mammillary-like protrusions of microbialites into the surrounding sediment, suggesting active growth of microbialite-producing organisms. Aggregations of terebellid worm tubes show a highly irregular relief, with tubes placed sub-parallel to the ancient sea floor. The presence of fibrous rim cement, crystal silt, and in some cases fragmentation of the tubes, suggest at least moderately energetic waters. Aggregations are thus interpreted as preserved in situ, but not in toto. The entire complex was probably deposited at the margin or upper slope of a carbonate platform. Although the presence of a large number of terebellids associated with microbialites boundstone may indicate some sort of environmental stress, such a stress remains to be identified.     

Paleoecology of Middle Ordovician stromatoporoid mounds in Vermont

Fossiliferous mounds of carbonate mud are a distinctive facies in the middle Chazy Group (Crown Point Formation) at Isle La Motte, Lake Champlain. The mounds are surrounded by bedded calcarenite of spar-cemented pelmatozoan debris. Channels which cut into the mounds during mound growth are filled with the same calcarenite. The mud-free intermound rocks and the mound biota suggest agitated, normal marine shallow-water environments. The principal lime-secreting organisms within the mounds are stromatoporoids, calcareous algae, tabulate corals, sponges, and bryozoans. Each mound is dominated in terms of biomass by one of three groups: stromatoporoids, calcareous algae, and bryozoans. Most of the mound biota first appear at the base of the Crown Point Formation. In the lower Crown Point Formation the organisms increase in number and species. Both changes in the biota are related to periods of shallowing of the Chazy sea which are also reflected in the character of the carbonate sands.