Stromatolite biostromes and associated facies in the late precambrian porsanger dolomite formation of Finnmark,Arctic Norway

The Late Precambrian Porsanger Dolomite Formation, occurring beneath the Varanger tillite in Arctic Norway, consists of various dolomitic lithofacies of subtidal, intertidal and supratidal environments. The lithofacies belong to three facies associations, A, B and C, which are repeated several times in the sequence. Facies association A comprises cryptalgal laminites, dolomicrites and thin-bedded grainstones and flakestones. The environment represented by this facies is broadly intertidal (locally supratidal) flat, with the interbedded carbonate sands representing storm deposits. Facies association B, of shallow subtidal to low intertidal origin, comprises cross-bedded carbonate sands (flakestones, grainstones and oolites) forming units up to 10 m thick. Small stromatolite bioherms (5 m wide, 2 m high) are locally developed within these “high-energy” deposits. Facies association C formed in a subtidal environment consists of laterally extensive (over 20 km) uniformly developed stromatolite biostromes, up to 16 m thick. The biostromes, locally divided by channels filled with grainstones and intraformational conglomerates, are composed of cylindrical and turbinate columnar (SH-V and SH-C) and digitate stromatolites (Gymnosolen, Inseria and Tungussia) in their lower parts. Larger, bulbous (SH-C and LLH-C) and conical (Conophyton) stromatolites occur in the upper parts, as well as the branching conophyte, Jacutophyton.All of the biostromes are always developed above cross-bedded carbonate sands (facies association B). A broadly symmetrical cyclic pattern, A B C B A, of tidal flat deposits (facies association A) passing up into carbonate sands (B), into biostrome (C), overlain by carbonate sands (B) and then tidal flat deposits (A), is repeated four times in the Porsanger Dolomite sequence. The pattern is interpreted in terms of two controls on sedimentation: (1) a slow transgressive phase followed by (2) depositional regression. The former (1) took place either through eustatic sea-level rise or more likely through accelerated subsidence because of tectonic instability and compaction of underlying sediments. This resulted in the sequence: tidal flat sediments, low intertidal/shallow subtidal carbonate sands, subtidal biostrome (A, B, C). Depositional regression through prograding tidal flats, generated the shoaling upward part of the cycle: biostrome, carbonate sands, tidal flat sediments (C, B, A).     

Pleistocene facies of Belize barrier and atoll reefs

The knowledge of Pleistocene reef facies of Belize, Central America, is largely limited to outcrops in the northernmost part of the country. Otherwise, Pleistocene limestone, which forms the basement of the modern barrier and atoll reefs, occurs in the subsurface and is to a major extent unstudied. Based on the study of 40 m of core from 25 rotary core holes collected on central and southern Belize barrier and on atoll reefs, five Pleistocene reef facies are distinguished in the present study. They include (1) Acropora palmata grainstone, (2) Acropora cervicornis grainstone, (3) biogenic grainstone, (4) mollusk packstone, and (5) mollusk-foram wackestone. Facies 1 and 3 occur on marginal reefs, facies 2 is found on marginal and lagoonal reefs, and facies 4 and 5 mark lagoon shoals and lagoons, respectively. Most of the facies have equivalents in the Pleistocene of the wider Caribbean and also in the modern of the study area. Diagenetic features include dissolution, caliche formation, laminated blocky low-magnesium-calcite and dogtooth spars. Age data from Pleistocene corals obtained during earlier studies are discussed, and indicate deposition during marine isotope stage 5, between 140–80 ka bp.     

The upper Moscovian and basal Kasimovian (Pennsylvanian) of Central European Russia: Facies,subaerial exposures and depositional model

Summary The type upper Moscovian-basal Kasimovian argillaceous-carbonate succession of central European Russia contains regionally traced cyclothem-bounded subaerial exposure horizons (geosols) represented mainly by rendzina-type palaeosols. Palaeokarst profiles occurrarely and grade laterally to palaeosols. Composite subaerial profiles divided by one or two thin marine beds are called ‘multiple geosols’. The biofaces structure of the studied succession is defined by brachiopod and fusulinoid biofaces. The heterogeneous Choristites biofacies characterizes openmarine intervals, which constitute the bulk of the succession, and is defined by presence of Choristites. The Meekella biofacies with monospecific concentrations of Meekella shells and extreme rarity of other brachiopods characterises restricted peritidal intervals which commonly constitute the terminal regressive parts of major cyclothems. Three fusulinoid biofacies defined by Baranova and Kabanov (2003) include restricted peritidal Biofacies 1 with only small fusulinoids Fusiella and Schubertella present, open shoal-to-subtidal Biofacies 2 with the richest fusulinoid assemblages, and the most offshore Biofacies 3 with less diverse, sometimes Hemifusulina-dominated, fusulinoid assemblages. Bioturbation patterns and ichnofossils allow recognition of deeper subtidal Zoophycos and shallower non-Zoophycos ichnofacies. Among the latter, shallowest subtidal facies are characterized by presence of thalassinoid burrows. Intertidal laminated lithofacies with suppressed bioturbation contain Skolithos burrows. Seventeen lithofacies are recognized. Terrestrial lithofacies include topclays (upper clayey palaeosol horizons) and aeolian grainstones. Restricted peritidal lithofacies include cross-stratified skeletal-peloidal grainstones, fine-grained laminated grainstones-mudstones, and lagoonal mudstones. Open shoal lithofacies include ooidal grainstones (rare, only in Podolskian) and coarse skeletal-peloidal grainstones. The open subtidal lithofacies include skeletal packstones-rudstones, shallow subtidal packstones-wackestones, deeper subtidal packstones-wackestones, Ivanovia boundstones (only in Podolskian), proximal tempestites, distal tempestites, and skeletal wackestones-mudstones. The fossiliferous shale lithofacies is a miscellaneous group of marine shales lacking distinct features of the above-listed lithofacies. Conglomerates of cyclothem bases that are regarded as early transgressive lithofacies are variable in their palaeoenvironmental position and are characterized by concentrated pebbles derived from palaeosol reworking. The shallowest subtidal lithofacies of fine packstones-grainstones is considered as transitional between open subtidal and restricted peritidal lithofacies. The origin of stratiform dolostones is shown to be early diagenetic in the subsurface. The depositional model involves a shallow and broad epicontinental ramp, where through water circulation prevented stratification of the water column and allowed large skeletal benthos to colonize the entire spectrum of depositional environments. Storms are thought to be the principal water-mixing agent. The anti-estuarine circulation carrying oxygenated waters down-ward may explain the lack of anoxic features in the deepest facies that may have formed below storm wave base.     

Palaeoecological significance of calcimicrobial communities during ramp evolution: An example from the Lower Cambrian of Germany

Summary The palaeoecology of calcimicrobial communities from the only Gondwana-related Lower Cambrian in Central Europe (eastern Germany, carbonates and siliciclastics) has been studied. Six morphological groups of calcimicrobes are described. Some of them show a significant ability for sediment stabilization and construction of biohermal reef mounds. Other types of calcimicrobes were more common in biostromal thickets. Some of them were capable of populating different environments, growing in different modes and on different substrates. AnEpiphyton-archaeocyathan reef mound is described, illustrating the importance of calcimicrobes for mound formation. The fossil communities together with a complex of sedimentary features allow a reconstruction of the depositional history of the environment. Based on comparison with similar Gondwanan Lower Cambrian successions (Sardinia/Italy, Spain) and facies development a model is proposed describing the sedimentary history. Three depositional stages are distinguished: (1) deep subtidal ramp, (2) shallow subtidal ramp, (3) shallow subtidal to intertidal mixed siliciclastic-carbonate ramp with migrating oolitic shoals. In spite of similarities with the deposits in southern Europe, some distinct differences exist with respect to the succession of facies, the completeness of the sections, the fossil spectrum, and the nature of the siliciclastic sediments. For the German Lower Cambrian, a facies development from a low energy deep environment to a high energy shallow environment (partly restricted and with some evaporites) can be reconstructed. As compared with Sardinia and Spain, the depositional environment of the eastern German Lower Cambrian successions was predominantly characterized by low-energy conditions.     

Sedimentation on Rasdhoo and Ari Atolls, Maldives, Indian Ocean

A first systematic study of composition, texture, and distribution of modern sediments in two Maldivian atolls reveals the predominance of skeletal carbonates. Fragments of corals, calcareous algae, mollusks, benthic foraminifera, and echinoderms are identified in the grain-size fraction >125 μm. Non-skeletal grains such as cemented fecal pellets and aggregate grains only occur in small percentages. Fragments of skeletal grains, aragonite needles, and nanograins (<1 μm) are found in the grain-size fraction <125 μm. Needles and nanograins are interpreted to be largely of skeletal origin. Five sedimentary facies are distinguished (1–5), for which the Dunham-classification is applied. Fore reef, reef, back reef, as well as lagoonal patch reef and faro areas in both atolls are characterized by the occurrence of coral grainstones (1), which also contain fragments of red coralline algae, the codiacean alga Halimeda, and mollusks. On reef islands, coral-rich sediment is cemented to form intertidal beachrock and supratidal cayrock. Skeletal grains in atoll-interior lagoons are mainly mollusks and foraminifera. The lagoon of Rasdhoo Atoll is covered in the west by mudstones (2), in the center by mollusk packstones (3) and mollusk wackestones (4), and by hard bottoms with corals in the east adjacent to channels through the atoll reef margin. The interior lagoon of Ari Atoll contains mollusk wackestones (4) in the center and mollusk-foraminifer packstones (5). Marginal lagoon areas are characterized by hard bottoms with corals. Facies distribution appears to be an expression of depositional energy, which decreases from the atoll margin towards the center in Ari Atoll, and towards the west in Rasdhoo Atoll. Predominant sediment mineralogies include aragonite and high-magnesium calcite. Mean aragonite content decreases from 90% in coral grainstone to 70–80% in mollusk packstone, mollusk wackestone, and mudstone, and to 50% in mollusk-foraminifer packstone. Stable isotopes of oxygen and carbon in bulk samples range from −3 to −1.5 (δ¹⁸O) and from +0.4 to +3.2 (δ¹³C). It is not possible to delineate facies based on O- and C-isotopes.     

Early (Series 2) Cambrian archaeocyathan reefs of southern Labrador as a locus for skeletal carbonate production

Pruss, S.B., Clemente, H. & Laflamme, M. 2012: Early (Series 2) Cambrian archaeocyathan reefs of southern Labrador as a locus for skeletal carbonate production. Lethaia, Vol. 45, pp. 401–410. Archaeocyathan reefs, the first reefs produced by animals, are prominent, global features of early Cambrian successions. However, microbialites – the dominant reef components of the Proterozoic – were still abundant in most archaeocyathan reefs. Although such reefs were a locus for carbonate production, it is unclear how much carbonate was produced skeletally. This analysis of well‐known early Cambrian archaeocyathan patch reefs of the Forteau Formation, southern Labrador, demonstrates that skeletal carbonate was abundantly produced in these archaeocyathan reefs, although only about half was produced by archaeocyathans. Trilobites, echinoderms and brachiopods contributed substantially to the total carbonate budget, particularly in grainstone facies flanking the reefs. Through point count analysis of samples collected from the reef core and flanking grainstones, it can be demonstrated that skeletal material was most abundant in grainstone facies, where animals such as trilobites and echinoderms contributed significantly to carbonate production. In contrast, microbial fabrics were more abundant than skeletal fabrics in the reef core, although archaeocyathan material was more abundant than other skeletal debris. Similar to modern reefs, these reefs created a variety of habitats that allowed for the proliferation of skeletal organisms living on and around the reef, thereby promoting skeletal carbonate production through ecosystem engineering. □Archaeocyatha, bioherms, carbonates, calcification, point count analysis     

Microbial-Activated Sediment Traps Associated with Oncolite Formation Along a Peritidal Beach,Northern Arabian (Persian) Gulf,Kuwait

Identification of microbial communities within shoreline sediments and sediment precipitates from the Tigris-Euphrates delta (northern Kuwait) were determined by microscopic/nanoscopic studies, and by molecular analysis. Oncolites are syn-diagenetic carbonate precipitates that are surviving in a shallow subtidal to intertidal siliciclastic environment with periodically excessive hydraulic energy, extreme salinity (up to 47 per mil), and high concentrations of organic matter. X-ray diffraction techniques reveal that oncolite cortices are predominantly composed of calcite, quartz, halite and dolomite, associated with minor fractions of clay minerals. Quantitative analysis of the Corey Shape Factor reveals distinct morphological populations but with local overlap. A plot of the Equivalent Diameter vs. Corey Shape Factor provided the best indicator of the morphological relationships within the total oncolite population, indicating a hydrodynamically controlled morphological distribution defining intertidal and subtidal oncolite classes. Direct microscopic examination of the samples indicates that diatoms are the most abundant eukaryotic algae in subtidal sediments and within actively precipitating carbonate cements, especially the genus Navicula. In contrast, filamentous cyanobacteria from the genus Anabaena are most abundant in the intertidal zone sediments. The PCR-DGGE of the 16SrRNA gene of the cyanobacteria shows a higher diversity for this genus of bacteria in all sediment samples and that the cyanobacterial population in the diagenetically precipitating oncolites are closely related to the population found in the subtidal sediments. Dunaliella viridis dominates the culturable algae obtained from the four tidal zones. Our results indicate that a range of microbial populations are actively contributing to the formation of microbially-induced sedimentary structures in the extreme conditions of the southern Tigris-Euphrates delta.     

An early cretaceous section in the Kircaova area (Berdiga Limestone,NE-Turkey) and its correlation with platform carbonates in W-Slovenia

Summary In the Kale (Gümüshane) area in the North Eastern Turkey, platform carbonates of the Berdiga Limestone were deposited during Late Jurassic-Early Cretaceous time in environments varying from intertidal to fore reef. The sequence shows extensive lateral and vertical alterations and interfingering of different facies types. In the upper part of the Berdiga Limestone in the Kircaova area a bituminous thin-bedded to platy limestone and shale 5 to 6 m thick occurs at the Early/Late Aptian boundary. It is underlain by limestones rich in silica nodules of up to 10 cm size. A facies analysis of a section about 70 m thick including the bituminous interval was carried out in 1994/95 at the SW border of the Kircaova area close to the road from L?rikas to Kale. The limestones consist mainly of packstones and grainstones locally rich in calcareaous algae and forminifera. Fragments of molluscs and echinoids as well as some ostracods and calcispheres occur. Some sponges, corals, and beds rich in molluscs occur in minor amounts in the middle part of the section which is characterized by intertidal to shallow subtidal facies. Algae and foraminifera indicate a Barremian-Early Aptian age of the lower part and Late Aptian age of the upper part of the section (e.g.Salpingoporellamuehlbergii, Salpingoporella aff.melitae, Clypeina solkani, Novalesia producta), divided by the bituminous limestones. In West Slovenia (close to the Italian border) a complete Cretaceous section occurs at Sabotin mountain containing Aptian beds with comparable faunal composition. In contrast to the Berdiga Limestone, in Slovenia at the rim of the dinaric platform a patch reef about 50 m in thickness is developed which is also covered by a bituminous limestones (black shale) marking the Early/Late Aptian boundary. Faunal elements in Slovenia arePalorbitolina lenticularis, Cuneolina laurentii, Orbitolina (Mesorbitolina) texana andSalpingopoprella dinarica. The bituminous limestone appears to be a marker horizon. At both locations it is locally rich in characeans probably indicating a regressive maximum before another transgression began in the Late Aptian/Albian as world-wide drowning event. Possibly the occurrence of the bituminous limestone (black shale) is associated with volcanic activity during the Aptian. If so it could be used as a chronostratigraphic marker horizon in both areas analyzed.     

A new species of the interstitial genus <Emphasis Type="Italic">Neopetitia</Emphasis> (Polychaeta,Syllidae, Eusyllinae) from Tenerife,with modified acicular chaetae in males

A new species of Neopetitia San Martín, 2003 is described from intertidal and shallow subtidal soft-bottom stations on the eastern and western coast of Tenerife, Canary Islands. The new species is characterized by the presence in males of a modified acicular chaeta in chaetiger 11. A discussion of known species of the genus is presented.     

Microfacies and sequence stratigraphy of the Amapá Formation, Late Paleocene to Early Eocene, Foz do Amazonas Basin, Brazil

On the basis of thin-section studies of cuttings and a core from two wells in the Amapá Formation of the Foz do Amazonas Basin, five main microfacies have been recognized within three stratigraphic sequences deposited during the Late Paleocene to Early Eocene. The facies are: 1) Ranikothalia grainstone to packstone facies; 2) ooidal grainstone to packstone facies; 3) larger foraminiferal and red algal grainstone to packstone facies; 4) Amphistegina and Helicostegina packstone facies; and 5) green algal and small benthic foraminiferal grainstone to packstone facies, divisible locally into a green algal and the miliolid foraminiferal subfacies and a green algal and small rotaliine foraminiferal subfacies. The lowermost sequence (S1) was deposited in the Late Paleocene–Early Eocene (biozone LF1, equivalent to P3–P6?) and includes rudaceous grainstones and packstones with large specimens of Ranikothalia bermudezi representative of the mid- and inner ramp. The intermediate and uppermost sequences (S2 and S3) display well-developed lowstand deposits formed at the end of the Late Paleocene (upper biozone LF1) and beginning of the Early Eocene (biozone LF2) on the inner ramp (larger foraminiferal and red algal grainstone to packstone facies), in lagoons (green algal and small benthic foraminiferal facies) and as shoals (ooidal facies) or banks (Amphistegina and Helicostegina facies). Depth and oceanic influence were the main controls on the distribution of these microfacies. Stratal stacking patterns evident within these sequences may well have been related to sea level changes postulated for the Late Paleocene and Early Eocene. During this time, the Amapá Formation was dominated by cyclic sedimentation on a gently sloping ramp. Environmental and ecological stress brought about by sea level change at the end of the biozone LF1 led to the extinction of the larger foraminifera (Ranikothalia bermudezi).     

Relationship between algae and environment: an Early Cretaceous case study, Trascău Mountains, Romania

The relationship between algae and depositional environment was studied in a limestone succession of Berriasian–Valanginian age. Several depositional environments were recorded from shallow subtidal to intertidal and supratidal, with salinity ranging from normal marine to fresh and/or supersaline water. The algal assemblages consist mainly of dasycladaleans, rivulariacean-type cyanobacteria and charophytes. Nipponophycus (Bryopsydales) and Lithocodium-Bacinella (microproblematicum), occur at some levels. Dasycladaleans are associated with subtidal, sometimes restricted (“lagoonal”) environments, while rivulariacean-like cyanobacteria and charophytes characterise intertidal-supratidal and fresh and/or supersaline environments, respectively. Among the dasycladaleans, Salpingoporella annulata is often related to restricted environments where it forms monospecific assemblages. Large dasycladaleans, such as Selliporella neocomiensis, Macroporella praturloni and Pseudocymopolia jurassica are found in subtidal high-energy deposits (bioclastic grainstones). The relationship between environment and algae, characteristic for each depositional unit, can be used to interpret the relative sea-level variations.     

Early Triassic peritidal carbonate sedimentation on a Panthalassan seamount: the Jesmond succession,Cache Creek Terrane,British Columbia,Canada

The Jesmond succession of the Cache Creek Terrane in southern British Columbia records late Early Triassic peritidal carbonate sedimentation on a mudflat of a buildup resting upon a Panthalassan seamount. Conodont and foraminiferal biostratigraphy dates the succession as the uppermost Smithian to mid-Spathian. The study section (ca. 91 m thick) is dominated by fine-grained carbonates and organized into at least 12 shallowing-upwards cycles, each consisting of shallow subtidal facies and overlying intertidal facies. The former includes peloidal and skeletal limestones, flat-pebble conglomerates, stromatolitic bindstones, and oolitic grainstone, whereas the latter consists mainly of dolomicrite. The scarcity of skeletal debris, prevalence of microbialite, and intermittent intercalation of flat-pebble conglomerate facies imply environmentally harsh conditions in the mudflat. The study section also records a rapid sea-level fall near the Smithian-Spathian boundary followed by a gradual sea-level rise in the early to mid-Spathian.     

Foraminiferal biofacies eco-succession and Holocene sealevels,Port Pirie,South Australia

At Port Pirie, on the eastern coast of Northern Spencer Gulf, South Australia, 10 cores taken along a 3 km transect recovered a succession of Holocene marine sediments. Facies representing shallow subtidal Posidonia seagrass and intertidal sandflat, mangrove and back-storm ridge coastal lagoon environments are recognized on the basis of lithological characteristics and their preserved foraminifera. An assemblage dominated by Nubecularia lucifuga, Peneroplis planatus and Discorbis dimidiatus signifies sediments of shallow subtidal Posidonia seagrass meadows. Subtle changes in the numerical distribution of these species upcore are used to infer the change from subtidal to intertidal sandflat facies; Elphidium crispum and Elphidium macelliforme become more numerous across this transition. The mangrove facies is characterized by Trochammina inflata. This species is present significantly in only one seaward core where modern mangrove woodland continues to grow today and no equivalent biofacies are recognized in other cores. The lagoonal sediments preserve a rich assemblage of species of euryhaline foraminifera. Together with those of the mangrove woodland, they exhibit an ecological succession which can be related to decreasing intervals of tidal inundation and increasing salinity. Helenina anderseni, with subordinate Ammonia beccarii, and Elphidium cf. articulatum are the pioneer species in the euryhaline setting, giving way to Trichohyalus tropicus and Miliolinella schauinslandi. Late stages of hypersaline sedimentation are characterized by Triloculina inflata+Triloculina oblonga. In the mangroves, H. anderseni, A. beccarii and Elphidium cf. articulatum are replaced by Trochammina inflata as the dominant species. In turn, as further sediment aggradation leads to ever shorter intervals of tidal inundation at the landward side of the mangrove woodland, Trochammina inflata is overtaken by Ammobaculites barwonensis. Quantitative foraminiferal biofacies analysis confirms and refines the sedimentological interpretation of intertidal sediment facies from macro-observations of the core materials. It provides independent estimates of the elevation of key facies boundaries in cores and confirmation of a general relative fall in sealevel in Northern Spencer Gulf over the past 7000 yr.     

Pleistocene marine depositionalenvironments from Mauritius island,Indian Ocean

The Pleistocene elevated marine carbonate complexes on Mauritius island correspond to three types of depositional zones: (1) reef-crest zone, (2) backreef zone, (3) littoral zone.On reef crests, the primary frame-builders are scleractinian corals (Acroporidae, Faviidae, Poritidae) and crustose coralline algae. The secondary builders are encrusting Foraminifers (Homotrematidae) chiefly, Molluscs (Vermetidae), Bryozoans (Cheilostomata) and Serpulids. Associated internal sediments are coarse to fine sand-sized grainstones or packstones and wakestones. In decreasing order of abundance, skeletal elements include fragments of corals, branched and crustose red algae, Pelecypods, Gastropods, benthonic Foraminifera (Amphisteginidae, Peneroplidae, Calcarinidae, Nummulitidae, Alveolinidae and Homotrematidae), Echinoderms and Alcyonarians; the most abundant mud-sized grains are identified as tunicate spicules. Primary marine cements are needle, palisade, micrite and pelletal ones.The backreef zone is characterized by coarse tomedium grainstones, packstones and wakestones. In addition to pellets the most common components are skeletal in nature; they broadly show the same mode of occurrence as the reef-crest unit. Primary cements locally occur in packed fibrous or micrite form.In littoral areas, well-sorted grainstones to poorlysorted mudstones can be described. The distribution of the various categories of biogenic particles is dependent upon the extent of reef tracts; ancient beaches from narrow reefs are characterized by coralgal facies while consolidated muddy banks in large complexes display high amount of molluscan detritus. Primary cementation appears mainly to be the result of the precipitation of fibrous or micrite calcite.The morphology, biological associations andsediments of these Pleistocene limestones are homologous with those of the adjacent modern environments.     

Facies mosaic in the inner areas of a shallow carbonate ramp (Upper Jurassic,Higueruelas Fm,NE Spain)

The internal facies and sedimentary architecture of an Upper Jurassic inner carbonate ramp were reconstructed after the analysis and correlation of 14 logs in a 1 × 2 km outcrop area around the Mezalocha locality (south of Zaragoza, NE Spain). The studied interval is 10–16 m thick and belongs to the upper part of the uppermost Kimmeridgian–lower Tithonian Higueruelas Fm. On the basis of texture and relative proportion of the main skeletal and non-skeletal components, 6 facies and 12 subfacies were differentiated, which record subtidal (backshoal/washover, sheltered lagoon and pond/restricted lagoon) to intertidal subenvironments. The backshoal/washover subenvironment is characterized by peloidal wackestone–packstone and grainstone. The lagoon subenvironment includes oncolitic, stromatoporoid, and oncolitic-stromatoporoid (wackestone and packstone) facies. The intertidal subenvironment is represented by peloidal mudstone and packstone–grainstone with fenestral porosity. Gastropod-oncolitic (wackestone–packstone and grainstone) facies with intercalated marl may reflect local ponds in the intertidal or restricted lagoon subenvironments. Detailed facies mapping allowed us to document 7 sedimentary units within a general shallowing-upward trend, which reflect a mosaic distribution, especially for stromatoporoid and fenestral facies, with facies patches locally more than 500 m in lateral extent. External and internal factors controlled this heterogeneity, including resedimentation, topographic relief and substrate stability, combined with variations in sea-level. This mosaic facies distribution provides useful tools for more precise reconstructions of depositional heterogeneities, and this variability must be taken into account in order to obtain a solid sedimentary framework at the kilometer scale.     

Internal structure and paleoecology of the lower Permian Uzunbulak reef complex of the Tarim Basin,Northwest China

Summary The internal construction and biotic communities of the Uzunbulak reef of the northwestern Tarim Basin are studied for the first time. The reef was built during the Sakmarian, while the reef substrate and capping beds are of latest Asselian and earliest Artinskian ages, respectively. The reef substrate beds are composed of skeletal and oncoid grainstone. Those fusulinid-dominated skeletal shoals and oncoid banks indicate a high-energy environment and produced local topographic highs on which the reef grew. Reef framework consists mainly of calcisponge bafflestone, calcisponge-Thartharella framestone, and Tubiphytes, Archaeolithoporella and Girvanella boundstones. Calcisponges were the primary frameconstructors that baffled high-energy currents. Archaeolithoporella, Tubiphytes, Girvanella and possibly microbes acted as the primary binders for the boundstone framework. Fusulinids and brachiopods were common reef dwellers. The interreef facies sediments are composed of skeletal-crinoid wackestone-packstone. Most of bioclasts have thick, micritized envelopes. The back-reef facies deposits consist of alternating skeletal packstone to wackestone and black shale. Sea-level fluctuations were probably accountable for the reef growth and demise. Of the reefal dwellers, brachiopods are extraordinarily abundant in Uzunbulak. They are assignable to five distinctive associations, one each from the reef substrate, framework and inter-reef facies, respectively, and two from the reef capping facies. The brachiopods in the substrate beds were mostly attached to hard substrates by a pedicle, while a few species rested on soft substrates by support of halteroid spines. Cementation of the ventral valve on hard substrates characterizes attachment of the reef framework brachiopods. All inter-reef species were anchored into the substratum comprising hard material by a strong pedicle. Back-reef brachiopods dominantly rested on the soft substrates by support of halteroid spines. the framework brachiopods had the strongest wave-resistant capability;those from both substrate and inter-reef facies were moderately capable of withstanding agitation; and the backreef species preferred to live in calmwater, organic-rich muddy environments.     

A late-devonian (Famennian)Renalcis-Epiphyton reef at Zhaijiang, Guilin, South China

Summary Microbial reefs, together with stromatolitic mounds and ooid shoals, constitute massive limestones in Famennian platform marginal strata in Guilin, in sharp contrast to the well-known coral-stromatoporoid reefs in the Givetian and Frasnian. Microbes played a significant and important role as stabilizers in the Famennian carbonate deposits of Guilin. A reef at Zhaijiang was constructed byEpiphyton andRenalcis, and is representative of such carbonate buildups. The reef is situated 10 km west of Guilin and corresponds to a microbe-dominated platform margin carbonate complex. Organisms in the Zhaijiang microbial reef are low diversity and dominated by ostracods and two genera of microbes,Epiphyton andRenalcis. Other microbial genera such asSphaerocodium andWetheredella occur in most of reef facies in Guilin, but their role as reef builder is doubtful because they occur only in minor amounts. The same four genera occur in volumetrically significant amounts in the upper Devonian carbonate complexes of Alberta. Canada and Western Australia. However.Epiphyton is more abundant in the Guilin reefs. The Zhaijiang microbial reef developed above Famennian proximal slope faices, as suggested by reef architecture and paleogeographic setting. The facies sequence of the microbial reef can be divided into three parts. The lower part is composed of medium-bedded bioclastic grainstones with a few microbial framestone lithoclasts, representing a proximal slope facies. The middle part consists of thin-bedded mudstone and shale with limestone lenses that are thought to be low stand deposits. In some cross sections, mudstone and shale infilled tidal channels that developed in the bioclastic grainstones.Renalcis-Epiphyton framestone constitutes the upper part with massive stacking patterns. The reef is 35 m thick and over 50 m in width. Nine litho- and biofacies are recognized. Zhaijiang reef provides an example of a binder guild-dominated buildup in the almost vacant reef ecosystem of the Famennian and represents a characteristic kind of reef after the Frasnian/Famennian extinction.     

Facies and palaeoecology of Upper Jurassic (Middle Oxfordian) coral reefs in England

Summary This study documents the facies and fauna of Late Jurassic (Middle Oxfordian) coral reefs in England. Sedimentological and palaeoecological analysis of these reefs distinguishes three generic reef types: (1) small reef patches and thickets associated with siliciclastic deposits; (2) small reef patches and thickets associated with siliciclastic-free bioclastic grainstones and packstones; and (3) biostromal units associated with deep water facies. The depositional environments of these reef types are discussed. Two coral assemblages are identified: (1) the microsolenid assemblage; and (2) theThamnasteria, Isastraea, Fungiastraea andThecosmilia assemblage (Thamnasteria assemblage). TheThamnasteria assemblage developed in all shallow water environments in the study area, regardless of local environmental conditions. The fauna is very eurytopic,r-selected and can tolerate significant environmental fluctuations on short temporal scales (sub-seasonal). The main control on the development of the microsolenid assemblage was low light intensity, low background sedimentation rates and low hydrodynamic energy levels.     

Reef to basin sediment transport using Halimeda as a sediment tracer,Grand Cayman Island,West Indies

Fragments of the calcareous green alga Halimeda form a large part of the sediment in the fringing reef system and adjacent deep marine environments of Grand Cayman Island, West Indies. Nine species combine to form three depth-related assemblages that are characteristic of the major reef-related environments (lagoonpatch reef, reef terraces, and deep reef). These modern plant assemblages form the basis of the use of Halimeda as a sediment tracer. Halimeda-based tracer studies of Holocene sediments indicate that only sediments containing deep reef species of Halimeda are presently being transported through the reef system by sediment creep and being deposited at the juncture of the upper and lower island slope. Sediments containing shallow reef Halimeda are retained within the reef and lithified by marine carbonate cements. Tracer studies of Pleistocene sediment indicate large amounts of reef-derived carbonate sand containing deep water Halimeda were produced during interglacial high stands of sea level. Much of this material was removed by turbidity currents moving out of the reef system to the island slope down submarine channels perpendicular to the reef trend. These channels may still be identified on bathymetric profiles, but are no longer receiving coarse reef debris and are veneered with a blanket of pelagic carbonate mud.     

Subtropical coral-reef associated sedimentary facies characterized by molluscs (Northern Bay of Safaga, Red Sea, Egypt)

Summary The shallow marine subtropical Northern Bay of Safaga is composed of a complex pattern of sedimentary facies that are generally rich in molluscs. Thirteen divertaken bulk-samples from various sites (reef slopes, sand between coral patches, muddy sand, mud, sandy seagrass, muddy seagrass, mangrove channel) at water depths ranging from shallow subtidal to 40m were investigated with regard to their mollusc fauna >1mm, which was separated into fragments and whole individuals. Fragments make up more than 88% of the total mollusc remains of the samples, and their proportions correspond to characteristics of the sedimentary facies. The whole individuals were differentiated into 622 taxa. The most common taxon,Rissoina cerithiiformis, represented more than 5% of the total mollusc content in the samples. The main part of the fauna consists of micromolluscs, including both small adults and juveniles. Based on the results of cluster-, correspondence-, and factor analyses the fauna was grouped into several associations, each characterizing a sedimentary facies: (1) “Rhinoclavis sordidula—Corbula erythraeensis-Pseudominolia nedyma association” characterizes mud. (2) “Microcirce sp.—Leptomyaria sp. association” characterizes muddy sand. (3)”Smaragdia spp.-Perrinia stellata—Anachis exilis—assemblage” characterizes sandy seagrass. (4) “Crenella striatissima—Rastafaria calypso—Cardiates-assemblage” characterizes muddy seagrass. (5) “Glycymeris spp.-Parvicardium sueziensis-Diala spp.-assemblage” characterizes sand between coral patches. (6) “Rissoina spp.-Triphoridae —Ostreoidea-assemblage” characterizes reef slopes. (7) “Potamides conicus—Siphonaria sp. 2—assemblage” characterizes the mangrove. The seagrass fauna is related to those of sand between coral patches and reef slopes with respect to gastropod assemblages, numbers of taxa and diversity indices, and to the muddy sand fauna on the basis of bivalve assemblages and feeding strategies of bivalves. The mangrove assemblage is related to those of sand between coral patches and the reef slope with respect to taxonomic composition and feeding strategies of bivalves, but has a strong relationship to those of the fine-grained sediments when considering diversity indices. Reef slope assemblages are closely related to that of sand between coral patches in all respects, except life habits of bivalves, which distincly separates the reef slope facies from all others.