Shell disintegration and taphonomic loss in rudist biostromes

Radiolitid biostromes in the Upper Cretaceous of Austria and Italy record a marked taphonomic loss controlled mainly by the composition of the biocoenosis, by the density of rudist colonization, by the style of radiolitid shell disintegration and by early diagenetic processes. Radiolitid shells consisted of a calcitic ostracum and an originally aragonitic hypostracum. The attached valve of most radiolitids was built of (1) an outermost ostracal layer of delicate calcite lamellae, (2) a thick layer of ‘boxwork ostracum’ built of radial funnel plates and cell walls, (3) a thin, inner ‘ostracal layer 3’ of thick-walled boxwork, and (4) the hypostracum that formed the innermost shell layer. The attached valve disintegrated by spalling of radial funnel plates of layer 2, and by selective removal of the boxwork ostracum. In the free valve, the ostracum consisted of two layers: (a) an inner, lid-shaped layer of dense calcite, and (b) an outer layer composed of calcite lamellae. The free valve disintegrated by spalling into ostracal and hypostracal portions, by spalling of the ostracum into layers a and b, and by disintegration of layer b into packages of calcite lamellae and individual lamellae. The specific style of disintegration of the radiolitids was aided or induced by discontinuities in shell structure. Lamellar fragments from the ostracum of the upper valve and from the radial funnel plates of the lower valve locally are abundant in free-valve-funnel-plate floatstones that comprise the matrix of or occur in lenses within radiolitid biostromes. In biostromes with an open parautochthonous fabric, selective removal of the boxwork ostracum of the attached valve occurred by mechanical spalling and, most probably, by early diagenetic dissolution. Complete removal of the boxwork ostracum yielded thin, relict shells composed of the ‘ostracal layer 3’ and the hypostracum. During early diagenesis, the hypostracum was replaced by blocky calcite spar, or was dissolved and became filled by internal sediments. The combination of both selective removal of boxwork ostracum and early diagenetic dissolution of aragonite locally resulted in the formation of ghost biostromes that entirely or largely consist of faint relics of radiolitids. The syndepositional formation of radiolitid shell relics and the presence of radiolitid ghost biostromes produced by bios-tratinomic and early diagenetic processes show that rudist biostromes can undergo marked taphonomic loss during fossilization. The presence of ghost biostromes with a burrowed, open parautochthonous rudist fabric indicates that the final preservation of a rudist biostrome was directly influenced by the characteristics of the biocoenosis, including unpreserved burrowing taxa. Rudist biostromes may be of markedly different taphonomy as a result of the taxonomic composition of the entire assemblage and the density of colonization by the rudists.     

Biotic interaction and synecology in a Late Cretaceous coral-rudist biostrome of southeastern Spain

A coral-rudist biostrome exposed in Campanian limestones near the village of Tabernas de Valldigna in south-east Spain was analysed with respect to its palaeontology, sedimentology and palaeoecology. Special attention was given to possible evidence for synecological interactions between corals and rudists. Changes in the rudist shell accretion process are evident in some polished slabs and thin sections and resulted from in vivo contact with coral-colonies. These unusual balcony-like shell protuberances exist where the rudist’s commissure was in contact with corals. They likely represent defence-reactions of rudists against the coral cnidia. Nevertheless, the fossil record of these biotic interactions is rare. This may be due to different growth-rates of rudists and corals, differing shape and size of interacting areas, or different life-spans. In consequence, the discrete ‘window’ of intergroup biotic interaction was small. Sedimentation and resuspension rates were high in the biostrome and corals only established pioneer associations under these unfavourable conditions. A higher diversity of corals is reached, however, when rudists are present. This increase in diversity resulted from the availability of additional ecological niches such as rudist-shell hard substrates and elevation above mobile sediment surface. Rudists on the other hand, received support from stabilisation of their shells through coral encrustation and framework building. In consequence, both groups benefited from their co-existence.     

Stratigraphic architecture of a Santonian mixed siliciclastic-carbonate succession (Catalonian Pyrenees, Spain)

Summary At Collades de Bastus, Catalonian Pyrences, a Santonian mixed siliciclastic-carbonate succession indicates two proximal-distal gradients, and records two styles of stratigraphical development upon relative sea-level change. The succession consists of four small-scale sequences (5.1 to 5.4) within the highstand systems tract of the. “Valicarca-5” depositional sequence of Simo (1993), and is topped by a drowning sequence (small-scale sequence 5.5). The investigated succession (Collades Member) accumulated near the margin of the south-Pyrenean shelf, shortly before development of the south-vergent Boixols thrust system. Deposition of the Collades Member commenced with moderate sea-level rise accompanied by increased siliciclastic input. In the larger, eastern outcrop sector the Collades Member consists of a succession of neritic marls with four intercalated intervals each deposited from a carbonate shelf. Each carbonate interval consists of stacked upward-shoaling cycles interpreted as parasequences. From bottom to top, most parasequences consist of a coral-sponge-rudist bioconstruction, a rudist biostrome, and bioclastic limestones. Depositional sequences 5.1 to 5.4 developed by overstep of shelf carbonates with neritic marls, corresponding to the transgressive systems tract (TST) and to part of the highstand systems tract(HST) The carbonate facies tract of the HST consists of stacked parasequences that become thinner up-section and record a westward component of progradation. Each highstand carbonate interval is overlain by a stack of carbonate parasequences that become thicker up-section and, down depositional dip, by neritic marls. Together, the upward-thickening parasequence stack and the laterally adjacent overlying succession of neritic marls comprise the TST and part of the HST of the successive sequence. The sequence boundary is the level of maximum shoaling within each carbonate shelf interval. The uppermost sequence 5.5 is a drowning sequence (cf. Simo 1993). In the western outcrop sector, the Collades Member consists of hummocky cross-laminated to bioturbated sandy calcarenites, of neritic marls and of relatively thin intervals of coral-sponge-rudist limestones. Sequence development may have started with deposition of sharp-based bedsets of sandy calcarenites that both eastward and up-section become thinner and grade into neritic marls. Together, the succession of sandy calcarenites and neritic marls may comprise the TST and, possibly, part of the HST. In the HST neritic marls and, locally, coral-sponge-rudist bioconstructions accumulated. Deposition of some calcarenite bedsets seems to have started near or closely after maximum progradation of each carbonate shelf in the eastern part of outcrop. The stratigraphic architecture of the Collades Member indicates, for the eastern outcrop sector, an east-west proximal-distal gradient, whereas the western sector records a west-east gradient. The opposite gradients result from outcrop intersection subparallel to oblique to general northward depositional dip, across two distinct shelf depositional systems.     

Upper cretaceous rudist and stromatoporid associations of Central Oman (Arabian Peninsula)

Summary Rudist and stromatoporid associations of the Campanian from Central Oman are nearly monospecific. They are dominated byDurania aff.nicholasi, Vaccinites vesiculosus, Torreites milanovici or phaceloid and massive stromatoporids. Several other rudist genera play a secondary role. The thickness of the associations is rarely more than one metre. Solitary corals do not occur in the associations. Colonial corals are less common, although they are up to 1 m high and show considerable diversity. There are no binders. The reef structure indicates variable hydrodynamic conditions. They are always associated with very shallow water. The pureDurania aff.nicholasi patches with large colonial corals andTorreites milanovici are presumably the most rigid structures. The near monospecific associations ofVaccinites vesiculosus are widely distributed. Although mostly preserved in situ, strong currents, presumably caused by tropical storms, have repeatedly impaired and interrupted growth. The specific growth characteristics of the shell of some rudists, especially the radiolitids, enable an estimation of the individual lifespan. Frameworks of approximately 1 metre thickness probably developed in ±100 years. The sediments of the complete sections are predominantly bioclastic.     

Palaeoecology of solitary corals in soft-substrate habitats: the example of Cunnolites (upper Santonian, Eastern Alps)

The upper Santonian Hofergraben Member (Eastern Alps) provides an example of a soft‐substrate habitat suited mainly for solitary corals (Cunnolites), for colonial forms of solitary coral‐like shape (Placosmilia, Diploctenium), and for colonial corals of high sediment resistance (e.g. Actinacis, Pachygyra). The Hofergraben Member consists mainly of silty‐sandy marls of wave‐dominated, low‐energy shore zone to shallow neritic environments. Substrates of soft to firm mud supported level‐bottoms of non‐rudist bivalves, gastropods, solitary corals, colonial corals, rudists, echinoids, and benthic foraminifera. Boring and/or encrustation of fossils overall are scarce. In the marls, Cunnolites is common to abundant. Both a cupolate shape and a lightweight construction of the skeleton aided the coral to keep afloat soft substrata. Cunnolites taphocoenoses are strongly dominated by small specimens (about 1–3 cm in diameter). Cunnolites was immobile and mostly died early in life upon, either, smothering during high‐energy events, rapid sedimentation associated with river plumes, or by toppling and burial induced by burrowing. Comparatively few large survivor specimens may show overgrowth margins interpreted as records of partial mortality from episodic sedimentation or tilting on unstable substrate. Scattered pits and scalloped surfaces on large Cunnolites may have been produced, in some cases at least, by predators (durophagous fish?). Post‐mortem, large Cunnolites provided benthic islands to corals, epifaunal bivalves and bryozoans. In a single documented case of probable in vivo contact of Cunnolites with the colonial coral Actinastraea, the latter prevailed.     

Carbonate facies evolution from the late albian to Middle Cenomanian in Southern Istria (Croatia): influence of synsedimentary tectonics and extensive organic carbonate production

Summary During the Late Albian, Early and Middle Cenomanian in the NW part of the Adriatic Carbonate Platform (presentday Istria) specific depositional systems characterised by frequent lateral and vertical facies variations were established within a formerly homogeneous area, ranging from peritidal and barrier bars to the offshore-transition zone. In southern Istria this period is represented by the following succession: thin-bedded peritidal peloidal and stromatolitic limestones (Upper Albian); well-bedded foreshore to shoreface packstones/grainstones with synsedimentary dliding and slumping (Vraconian-lowermost Cenomanian); shoreface to off-shore storm-generated limestones (Lower Cenomanian); massive off-shore to shoreface carbonate sand bodies (Lower Cenomanian); prograding rudist bioclastic subaqueous dunes (Lower to Middle Cenomanian); rudist biostromes (Lower to Middle Cenomanian), and high-energy rudist and ostreid coquina beds within skeletal wackestones/packstones (Middle Cenomanian). Rapid changes of depositional systems near the Albian/Cenomanian transition in Istria are mainly the result of synsedimentary tectonics and the establishment of extensive rudist colonies producing enormous quantities of bioclastic material rather than the influence of eustatic changes. Tectonism is evidenced by the occurrence of sliding scars, slumps, small-scale synsedimentary faults and conspicuous bathymetric changes in formerly corresponding environments. Consequently, during the Early Cenomanian in the region of southern Istria, a deepening of the sedimentary environments occurred towards the SE, resulting in the establishment of a carbonate ramp system. Deeper parts of the ramp were below fair-weather wave base (FWWB), while the shallower parts were characterised by high-energy environments with extensive rudist colonies, and high organic production leading to the progradation of bioclastic subaqueous dunes. This resulted in numerous shallowing- and coarsening-upwards clinostratified sequences completely infilling formerly deeper environments, and the final re-establishment of the shallow-water environments over the entire area during the Middle Cenomanian.     

The faunal structure of a mid-Cretaceous rudist reef core

The macrofaunal distribution of the mid-Cretaceous El Abra Limestone reef core is quantified from two measured sections in Taninul Quarry, San Luis Potosi, central Mexico. The faunal structure is transitional between typical Lower Cretaceous reefs dominated by corals with low-density rudist bivalve packing; and densely-packed, rudist-dominated Upper Cretaceous reefs. The macrofauna is predominantly associations of unconnected individuals of caprinid rudists, with a low diversity of other shelly mollusks and corals. An examination of the alternation of paleocommunities defined by the dominant caprinid taxa reveals no pattern of biotic succession within the reef core. Large-scale sedimentologic features of mud and debris content, coupled with rudist growth type, suggest that paleocommunities may have been physically controlled.     

Microbial carbonates and corals on the marginal French Jura platform (Late Oxfordian,Molinges section)

Molinges was located on an Upper Jurassic ramp system of low-energy regime that developed at the southern margin of the French Jura platform. The sedimentary succession is characterized by the transition from a mixed siliciclastic-carbonate to a carbonate depositional setting that occurred during a long-term shallowing-upward trend. The disappearance of siliciclastics is explained by a climatic change, from humid and cold to drier and warmer conditions, previously identified in Late Oxfordian adjacent basins. The base of the section shows marl-limestone alternations of outer ramp. In its middle part, the section displays oncolitic marls, coral-microbialite beds and oncolitic limestones that deposited in a mid ramp position. Finally, the upper section part is made of oolitic limestones of inner ramp. In outer- to mid-ramp settings submitted to terrigenous inputs, the stacking pattern of deposits and facies evolution allow the identification of elementary, small-, medium-, and large-scale sequences. Small amplitudes of sea-level variations probably controlled rapid shifts of facies belts and reef window occurrences. In small-scale sequences, the coral beds developed during periods of sea-level rise. The decreasing rate of sea-level rise is marked by the downramp shift of the oncolitic limestone belt that led to the demise of coral-microbialite beds. These bioconstructions are mainly represented by thin biostromes in which corals never reach great sizes. The coral assemblages mainly include the genera Enallhelia, Dimorpharaea, Thamnasteria, and some solitary forms (Montlivaltia and Epistreptophyllum). They suggest relatively low-mesotrophic conditions in marine waters during the edification of the primary framework. Relatively cold water temperatures and periods of more elevated nutrient contents are probably responsible of the reduced coral development and the formation of a large amount of microbialites.     

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.     

Reefal and mud mound facies development in the Lower Devonian La Vid Group at the Colle outcrops (León province, Cantabrian Zone, NW Spain)

In the locality of Colle (Cantabrian Zone, NW Spain), the upper part of the Valporquero Shale Formation (Emsian, La Vid Group) contains an interval of shales and marlstones (barren, greenish-grey shales and fossiliferous, greenish-grey or reddish shales/marlstones) with beds and packages of homogeneous and cross-bedded skeletal limestones. Metre-scale mud mounds and coral biostromes occur encased in the fossiliferous reddish and greenish-grey shale/marlstones, respectively, with the coral biostromes overlying conspicuous skeletal limestone bodies. These rocks were deposited on a carbonate ramp, ranging from above storm wave base for the cross-bedded skeletal limestones to below the storm wave base for the remaining deposits, organic buildups included. The vertical stacking of these facies and the occurrence of the two types of buildups are interpreted to reflect the interplay among several (possibly 4th and 5th) orders of relative sea-level variations, during a 3rd-order highstand. Coral biostromes occur in early 5th-order transgressive system tracts developed within late 4th-order highstand, and are interpreted to have thrived on a stable granular substrate (skeletal limestones) in non-turbid waters, being later aborted by the onset of muddy sedimentation. Biostrome features suggest that they developed under environmental conditions essentially different from those related to the sedimentation of their granular substrate. Mud mounds occur in 5th-order transgressive and early highstand system tracts tied to early 4th-order sea-level rise. Field relationships suggest that mud mounds grew coevally with muddy sedimentation, with high-frequency variations in carbonate vs. terrigenous mud sedimentation influencing their development.An erratum to this article can be found at     

The <Emphasis Type="Italic">Laluzia armini</Emphasis> (gen. et spec. nov.) ecosystem: understanding a deeper-water rudist lithosome from the Early Maastrichtian of Mexico

In the Lower Maastrichtian Cardenas Formation exposed at La Luz (State of San Luis Potosí, east-central Mexico), a shallowing-upwards mixed-clastic-carbonate sequence is exposed. The sequence passes from marls with thin siltstones, through lower and upper hippuritid-rudist-dominated intervals, and into a Durania-dominated interval. This succession shows an increase in grain size upwards and a progressive reworking of rudists upwards (preserved in life position, other than in distinct tempestites, in the lower part; invariably reworked/toppled in the upper part). Epibionts show a change from a serpulid–bryozoan assemblage in the lower sequence to a red algal–rhodolith assemblage in the upper part. Using these data, we argue that the sequence shows a change from a low-energy, relatively deep-water, nutrient-rich environment with low-light intensity in the lower part, to a high-energy, well-lit environment in the upper part. Two rudist species are present: a new multifold hippuritid rudist with cellular outer shell layer, Laluzia armini, that lacks pallial canals in its free valve and has a unique myocardinal pillar arrangement, in the lower part; and Durania in the upper part. Laluzia was adapted to low-energy, low-light, soft-bottom environments that were abundant within the lower part of the sequence exposed in the La Luz section—a very unusual environment for rudists.     

Microstratigraphy and taphonomy of rudist shell concentrations in Upper Cretaceous limestones,Cilento area (central-southern Italy)

Rudist bed type and distribution has been investigated in Upper Cretaceous limestones cropping out in the northern Cilento area (southern Italy). These limestones are dominated by fine-grained, peloidal, silty packstone in which rudist-rich beds are intercalated. An inner shelf environment may be inferred on the basis of the recognized sedimentary and taphonomic features. The rudist shell beds are characterized by low species diversity, with slight differences in abundance of a few species belonging to the Durania, Bournonia, Sauvagesia, Gorjanovicia and Biradiolites genera, which usually form oligo- or monospecific congregations. The internal fabric of these levels (i.e. orientation, arrangement, packing and sorting of the skeletal elements; internal microstratigraphy) has permitted us to distinguish two broad shell bed categories: (a) shell beds considered as “Primary Shell Concentration”, in which the shell concentration is essentially created by the behaviour of local shell producers, preserved in situ and in growth position; (b) shell beds considered as “Hydraulic Shell Concentration”, which were deposited under the influence of hydraulic processes and/or input of surrounding bioclastic sediments. The taphonomic analyses allowed us to highlight the role of some of the biotic and abiotic factors that controlled the distribution of the rudists in the various habitats. The increase of physical disturbance (especially hydrodynamism) is the primary difference between these shell bed categories. The establishment and development of the densest rudist congregations appear to be related to the accommodation space made available by means of relative sea level rise. The lowering of the sea level was often accompanied by the increased influence of waves and/or currents on the seabed and the consequent sediment disturbance and demise of the rudist lithosome, although other factors cannot be excluded.     

On Cretaceous bioconstructions: Composition and evolutionary trends of crust-building associations

Summary Bioconstructions are built by colonial to solitary sessile organisms which develop a variety of different morphologies due to genetic, ecologic, and environmental controls. Crust-building associations are groups of encrusting taxa within a community which predominantly serve as binders and cementers of bioconstructions (planooccupants), while constructing organisms predominantly build the frameworks (spatio-occupants). In the Cretaceous, the most important constructional elements were corals, stromatoporoids, chaetetids, and rudists which built thickets, biostromes, mounds, patch reefs, and occasionally bioherms. The crust-building associations were composed of corals, cyanophytes (including tubiphytoids), microproblematicum (Lithocodium/Bacinella), modern red algae (corallinaceans and peyssonneliceans), as well as some stromatoporoids and chaetetids. The combination of constructing and binding associations can be used to differentiate Cretaceous build-ups both temporally and in terms of ecologic succession. The development of tropical to subtropical carbonate platforms during the Cretaceous brought about a world-wide expansion of and innovation within bioconstructions. The major changes within bioconstructions consist of the increasing dominance of the rudists as framework constructors and the evolution of the modern red algae. The corals remained an essential element of reef constructional as well as of binding associations. The stromatoporoids and chaetetids, however, lost importance during the mid-Cretaceous. Other important qualitative changes were the evolution of the acervulinids (a massive encrusting foraminiferid) during Campanian to Maastrichtian time and the extinction of the rudists at the end of the Cretaceous. Cretaceous bioconstructions suffered significant periods of retrogradation during the following periods: the beginning of the Cretaceous, Cenomanian-Turonian, and Maastrichtian-Paleocene. These represent long-term evolutionary changes, and to date, there is at least for encrusting associations no evidence to corroborate the short-term mass extinction events commonly documented for these boundaries. These long-term changes appear to be controlled by the interaction of various over-riding factors (tectonism, paleogeographic changes, oceanic chemistry, climate, and sea-level fluctuations). Although for individual bioconstructions the primary controlling mechanisim can possibly be determined, this is impossible at a global scale given current levels of understanding of the intricate interactions of these various factors.     

Succession of rudistid lithosomes along the western coastal margin of the Iberian Basin (Coniacian,Castrojimeno Section,central Spain)

Rudistid lithosomes cropping out near Castrojimeno, at the northern margin of the Central System in north-central Spain, provide detailed information on their composition and structure, on their development and succession, and about their relationship with the Coniacian sequence stratigraphy framework of the Iberian Basin. Most rudist assemblages are oligospecific, with a dominant species, or monospecific. The radiolitids Biradiolites angulosus, Praeradiolites requieni, and Radiolites sauvagesi and the hippuritids Hippurites incisus and Vaccinites giganteus were identified. Radiolitids demonstrate wide intraspecific morphological variability. The following Riding’s structural categories of organic reefs are represented: segment reefs, spaced and close cluster reefs, and close cluster/frame reefs. Bioclastic beds of reworked rudist fragments occur below or in between the rudist reefs. The vertical succession of all five types of rudistid lithosomes distinguished evidences a shallowing-upward trend. Rudistid lithosomes developed on the coastal margin during the superposition of the highstand sea-level stage of third- and fourth-order depositional sequences.     

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.     

Cenomanian-Turonian rudists from Western Sinai, Egypt: Systematic paleontology and paleoecology

The Cenomanian-Turonian sequence is well exposed in western central Sinai and contains a considerable number of rudist species. The identified rudists belong to Radiolitidae, Hippuritidae and Requieniidae. Fifteen species are described, belonging to ten genera: Requienia, Toucasia, Apricardia, Radiolites, Eoradiolites, Praeradiolites, Sphaerulites, Sauvagesia, Hippurites, and Vaccinites. Eleven species are reported in the Cenomanian and four species in the Turonian. Within the Cenomanian, two new species are described: Requienia tortuosi and Eoradiolites lenisexternus. The genus Requienia and the species Apricardia carentonenis d’Orbigny, Eoradiolites syriacus (Conrad), Sphaerulites agariciformis Delamétherie, Sphaerulites depressus Blanckenhorn and Vaccinites cf. grossouvrei (Douvillé) are reported for the first time from Egypt. The Cenomanian and Turonian rudists in the western Sinai show either elevator or clinger morphotypes, with the predominance of the former type; recumbent mode of life is rarely represented by some Requieniidae. The elevators are of isolated and clustered occurrences and more represented in the Cenomanian sequence. Rudists of the study area are mainly of parautochthonous fabrics with low to dense packing. Autochthonous fabrics are also achieved by some species, mainly in the Turonian. The disappearance of rudists from the middle part of the sequence and above the Cenomanian/Turonian boundary is due to a deeper setting that resulted from sea-level rise or seafloor subsidence (shelf drowning). The occurrence of rudists with oysters and other benthic fossils in the siliciclastic and carbonate sediments of the Cenomanian and Turonian sedimentary rocks in the Sinai indicate that the sequence was deposited on a broad, shallow shelf. Although the first marine transgression invaded the central Sinai in the late Cenomanian, transgressive deepening conditions continued until the Turonian. The rudists of central Sinai are of Tethyan affinity with significant relation with North Africa, the Middle East, and Southern Europe.     

Anthracoporella mounds in the Late Carboniferous Auernig Group,Carnic Alps (Austria)

Summary A heretofore undocumented example of skeletal mounds formed by the dasycladacean algaAnthracoporella spectabilis is described from mixed carbonate-clastic cycles (Auernig cyclothems) of the Late Carboniferous (Gzhelian) Auernig Group of the central Carnic Alps in southern Austria. The massive mound facies forms biostromal reef mounds that are up to several m thick and extend laterally over more than 100 m. The mound facies is developed in the middle of bedded limestones, which are up to 16 m thick. These limestones formed during relative sea-level highstands when clastic influx was near zero. The mound facies is characterized by well developed baffler and binder guilds and does not show any horizontal or vertical zonation. Within the massive mound faciesAnthracoporella is frequently found in growth position forming bafflestones and wackestones composed of abundantAnthracoporella skeletons which toppled in situ or drifted slightly.Anthracoporella grew in such profusion that it dominated the available sea bottom living space, forming ‘algal meadows’ which acted as efficient sediment producers and bafflers. BecauseAnthracoporella could not provide a substantial reef framework, and could not withstand high water turbulence, the biostromal skeletal mounds accumulated in shallow, quiet water below the active wave base in water depths less than 30 m. The massive mound facies is under- and overlain by, and laterally grades into bedded, fossiliferous limestones of the intermound facies, composed mainly of different types of wackestones and packstones. Individual beds containAnthracoporella andArchaeolithophyllum missouriense in growth position, forming “micromounds’. Two stages of mound formation are recognized: (1) the stabilization stage when bioclastic wackestones accumulated, and (2) the skeletal mound stage when the sea-bottom was colonized byAnthracoporella and other members of the baffler and binder guilds, formingAnthracoporella bafflestones and wackestones of the mound facies. A slight drop in sea-level led to the termination of the mound growth and accumulation of organic debris, particularly calcareous algae, fusulinids, crinoids and bryozoans, forming well bedded limestones, which overlie the mound facies     

Devonian carbonate buildup facies in an intra-oceanic island arc (Tamworth Belt, New South-Wales, Australia)

Summary  Biohermal and biostromal buildups were investigated in late Early and Middle Devonian carbonate complexes of the Tamworth Belt. The buildup types and subtypes were studied in three regions (Yarramanbully, Sulcor and, Wyaralong') to clarify their paleo-environmental position. Two stages of development are recognized: Incipient bioherms and bioherms. Incipient bioherms are carbonate buildups with organisms which commonly form true bioherms. They dominate the sediment with small growth forms but are not prolific enough to build large bio-frameworks. Small nodular and globular stromatoporoids characterize the incipient bioherms and are interpreted as stunted growth forms. In one location (‘Wyaralong’) the coarse stromatoporoid calcarenite represents a fore-reef facies, at Sulcor a shallow subtidal setting with moderate water energy can be deduced. The bioherms can be sub-divided into stromatoporoid-, stromatoporoid-Stachyodes-, and stromatoporoid-rugose coral bioherms. Their variable composition probably reflects growth and deposition in different zones of a reef complex and/or different proximity to areas of denundation indicated by high siliciclastic input. In the Tamworth region true bioherms occur only in the Moore Creek Limestone Member (Middle Devonian), and not in older carbonate successions. Biostromes are sub-divided into (1) incipient biostromes with stromatoporoid-heliolitid biostromes and alveolitid biostromes; (2) aggregate biostromes withAmphipora andStachyodes biostromes; (3) stratified biostromes; (4) mixed aggregate/stratified biostromes. The different types of biostromes are not limited to specific time-intervals, but rather to environmental conditions.

Development of rudist lithosomes in the Coniacian–Lower Campanian carbonate shelves of central-southern Italy: high-energy vs low-energy settings

The Late Cretaceous shallow-water depositional areas of southern Tethys were complexes of unprotected shelves occupied by foramol assemblages that produced loose, diagenetically stable bioclastic debris not involved in significant in situ cementation processes. Both storm- and wind-induced currents and waves exercised a strong control on the distribution of the shifting biogenic sediments which covered the open sea-floor, constituting large coalescing sheets of winnowed fine to coarse skeletal sands. Rudists spread over all shelf sectors, from more open and external areas to more internal ones, occupying different substrata and furnishing the bulk of the skeletal component by means of bioerosion processes. They colonised mobile sediments giving rise to complex bodies with peculiar characteristics related to environmental parameters of the different sectors of the shelf. On the basis of detailed sedimentological, taphonomic and palaeontological data, we recognised two main rudist-rich depositional settings (‘end members’) in the southern Italy Senonian rudist-bearing successions. In successions pertaining to hypothesised marginal shelf sectors, characterised by high-energy regime deposits, rudist lithosomes are metric in thickness and lateral extent and lens-like in morphology, rich in bioerosion-derived skeletal sand and silt. Rudists are highly diversified. Large elongated cylindro-conical hippuritids (mostly pertaining to the genera Hippurites and Vaccinites), thick-shelled radiolitids and plagioptychids largely dominate. Rudists clustered in life position are subordinate; they often form small bouquets. More commonly these organisms appear fallen but only barely reworked. The rudist-rich bodies laterally pass into clean bioclastic grainstone in which sedimentary structures, related to current and/or storm erosional action, are common. No evidence of significant original relief of the rudist bodies in respect of the neighbouring sediment can be recognised. The submarine erosion and/or the high-energy processes operating presumably inhibited the aggradation of the tidal sediments above the marginal ones. As a consequence the vertical facies organisation shows widespread subtidal cycles, as commonly recognised in open shelves with ramp-like morphologies. In successions pertaining to more internal and/or low-energy sectors, rudist-rich beds rhythmically alternate with finer-grained foraminiferal limestones. Small elevator radiolitids with oligospecific diversity are dominant, mostly concentrated in clumps. Rudists in growth position are abundant, although a large quantity of shells appear toppled with little reworking. They may form laterally continuous biostromal shell beds. Sedimentary structures such as cross-lamination and gradation are only occasionally present. The resulting facies are commonly arranged in peritidal/shallow subtidal cycles in which evidence of subaerial (up to pedogenic modifications on a large and small scale) and, less frequently, submarine exposure is common. Intermediate successions have been recognised, characterised by deposits of silty-sand plains, which present intercalations of graded, bioclastic, storm-related beds. Sedimentological characteristics seem to document more open conditions in which submarine erosion was intermittently prevalent. In these successions rudist species that are commonly found both in high-energy and low-energy assemblages coexist.     

A coral-microbialite patch reef from the late jurassic (florigemma-Bank, Oxfordian) of NW Germany (Süntel mountains)

Summary Anin situ Oxfordian patch reef from the Süntel hills (florigemma-Bank, Korallenoolith, NW-Germany) is described. It is composed of an autochthonous reef core overlain by a ‘parautochthonous’ biostrome. The exposed reefal area amounts to about 20 m in lateral and up to 4 m in vertical direction. Nearly all major marine reefal fossil associations from the Tethyal realm are present. In the reef core two facies can be distinguished: (1)Thamnasteria dendroidea thicket facies and (2) thrombolite facies. The first facies is composed of a thin branched autochthonous coral thicket mainly constructed ofTh. dendroidea colonies with only a minor portion ofStylosmilia. Frequently, theTh. dendroidea branches laterally coalesce bridge-like forming a delicate initial framework which was subsequently reinforced by thick microbial coatings, that make up approximately 80% of the rock volume. This facies is an excellent example for microbialite binding in reefal architecture. Additionally, several generations of micromorphic and partly cryptic encrusting organisms settled on theTh. dendroidea branches and microbialite crusts. They successively overgrow each other and fill the space between the coral branches in the thicket forming a characteristic community replacement sequence. Initial colonization of theThamnasteria dendroidea took place on an oncoidic/bioclastic hardground. During this early phase of reefal development, microbialites also played an important role in stabilizing and binding the reef body. The thrombolite facies (2) occupying nearly the same volume of the reef body as facies type (1) consists of a thrombolitic microbialitic limestone which fills the interstice between the coral colonies. It shows a considerably lower faunal diversity than theTh. dendroidea facies. Numerous cavities are interspersed in the thrombolithe and are almost completely filled with dolomitized allomicrite. In contrast, microbialite and allomicrite adjacent to the reef core rarely reveal any dolomitized areas. Above the reef core, mostly toppledSolenopora jurassica thalli occur together with a few massiveIsastrea colonies forming a parautochthnous biostrome. They are inhabited by a low diverse assemblage of encrusting organisms. Microbialites are only rarely present in this biostromal unit. The patch reef is developed within a lagoonal limemud facies both separated by a sharp interface. In contrast, continuous facies transition exists between theSolenopora biostrome and adjacent deposits which are characterized by micritic to pelmicritic limestone sometimes with lenses of oncoids. Debris derived from the patch reef is only sporadically intercalated in the reef surrounding lagoonal sediments. Gastropods, bivalves, and dasycladalean algae dominate the lagoonal biota. Up-section following theSolenopora biostrome nerinean gastropods become the most abundant species amounting to a ‘Nerinea-bed’. This horizon moderately elevates above the patch reef indicating, that is arose above the surrounding sea floor forming a relief. The patch reef established on a secondary hardground probably released by a minor transgression and a nondepositional regime. It grew up on a well-illuminated sea floor only a few meters below sea level. Only a low background sedimentation rate and modest water circulation are assumed during reefal growth. These features characterize an open marine lagoon. A subsequent shallowing upwards trend caused emergence of the early lithifiedflorigemma-Bank sediments. In the following erosional phase the reef core,Solenopora biostrome and ‘Nerinea-bed’ were sharply cut. Paleokarst phenomena (karst solution of the rocks, selective leaching of the aragonitic corals) truncate the surface of theflorigemma-Bank. Released by a transgressive sea level, the paleokarst surface is densely inhabited by marine boring and encrusting organisms (oysters, serpulids). Karst cavities are filled with an oncoid-bearing bioclastic limestone with a large portion of siliciclastics. Theflorigemma-Bank is overlain by the reddish bioclastic sandstone of the ‘Zwischenfl?zregion’.