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Neodymium isotopes of central Mediterranean phosphatic hardgrounds reveal Miocene paleoceanography
Morphological variability of peteinoid acritarchs from the Middle Ordovician of Öland, Sweden, and implications for acritarch classification
Bryozoans from the lower Silurian (Telychian) Hanchiatien Formation from southern Chongqing, South China
Lithological dependence of aragonite preservation in monospecific gastropod deposits of the Miocene Mainz Basin: Implications for the (dia-)genesis of limestone–marl alternations
High-resolution correlation of the Homerian carbon isotope excursion (Silurian) across the interior of the Midland Platform (Avalonia), UK
Interplay of Autogenic and Allogenic Processes On the Formation of Shallow Carbonate Cycles in a Synrift Setting (Lower Pliensbachian, Traras Mountains, NW Algeria)
REVEALING THE GENESIS OF LIMESTONE-MARL ALTERNATIONS: A TAPHONOMIC APPROACH
Conodonts in Silurian hypersaline environments: Specialized and unexpectedly diverse
Graptoloid evolutionary rates track Ordovician–Silurian global climate change
A Revised 87 Sr/ 86 Sr Curve for the Silurian: Implications for Global Ocean Chemistry and the Silurian Timescale
Testing the limits of Paleozoic chronostratigraphic correlation via high-resolution (<500 k.y.) integrated conodont, graptolite, and carbon isotope (δ 13 C carb ) biochemostratigraphy across the Llandovery–Wenlock (Silurian) boundary: Is a unified Phanerozoic time scale achievable?
A Hirnantian (latest Ordovician) reefal bryozoan fauna from Anticosti Island, eastern Canada: taxonomy and chemostratigraphy
Front Matter
Fabric transitions from shell accumulations to reefs: An introduction with Palaeozoic examples
Abstract One unresolved conceptual problem in some Palaeozoic sedimentary strata is the boundary between the concepts of “shell concentration” and “reef”. In fact, numerous bioclastic strata are transitional coquina–reef deposits, because either distinct frame-building skeletons are not commonly preserved in growth position, or skeletal remains are episodically encrusted by “stabilizer” (reef-like) organisms, such as calcareous and problematic algae, encrusting microbes, bryozoans, foraminifers and sponges. The term “parabiostrome”, coined by Kershaw, can be used to describe some stratiform bioclastic deposits formed through the growth and destruction, by fair-weather wave and storm wave action, of meadows and carpets bearing frame-building (archaeocyaths, bryozoans, corals, stromatoporoids, etc.) and/or epibenthic, non-frame-building (e.g. pelmatozoan echinoderms, spiculate sponges and many brachiopods) organisms. This paper documents six Palaeozoic examples of stabilized coquinas leading to (pseudo)reef frameworks. Some of them formed by storm processes (generating reef soles, aborted reefs or being part of mounds) on ramps and shelves and were consolidated by either encrusting organisms or early diagenesic processes, whereas others, bioclastic-dominated shoals in barrier shelves, were episodically stabilized by encrusting organisms, indicating distinct episodes in which shoals ceased their lateral migration.
Abstract Shelled phosphorites of Early Cambrian age are common in the Avène-Mendic autochthonous unit (Marcory Formation) and the Mélagues nappe ( “Heraultia beds” of the Lastours Formation), northern Montagne Noire (France). Palaeogeographically, the concentration of phosphate took place along the shelf edge between a stable inner platform (southern Montagne Noire) and an unstable slope-to-basin sea floor preserved in the northern Montagne Noire. Petrography, back-scattered SEM (scanning election microscopy) and elemental mapping by EDS (energy dispersive system) show that the phosphorites were generated by repeated alternations of low sedimentation rates and condensation forming hardgrounds, in situ early diagenetic phosphogenesis, winnowing and polyphase reworking of previously phosphatized skeletons and hardground-derived clasts. The succession of repeated cycles of sedimentation, phosphate concentration and reworking led to multi event phosphate deposits rich in allochthonous particles. Associated accumulations of exhumed and reworked pyrite clasts reflect final deposition in a mainly dysaerobic substrate.
Anatomy of the Early Cambrian ‘La Sentinella’ reef complex, Serra Scoris, SW Sardinia, Italy
Abstract All bioherms from the Early Cambrian (Botoman) Matoppa Formation of the Nebida Group in SW Sardinia were previously thought to be dominated by Epiphyton. However, at “La Sentinella” (Serra Scoris Hill), they are composed of Girvanella, Razumovskia, Botomaella and Renalcis, with Epiphyton and archaeocyaths as accessory components. This association forms two unusual types of crust boundstone, consisting of stacked flat or curved crusts and saucer-like archaeocyaths delimiting shelter cavities. Dendrolitic Renalcis archaeocyath–cement boundstone caps the bioherm. Analysis of the La Sentinella reef complex and comparison with similar constructions from Mongolia (Zuune Arts, Salaany Gol), Nevada (Stewart's Mill, Battle Mountain), Mexico (Sonora) and China (Tianheban Formation) suggest that episodic deposition of fine-grained siliciclastic or carbonate sediment followed by periods of non-deposition enabled the calcimicrobial rafts and crusts to colonize the substrate and then provide synoptic relief for the development of a dendrolitic Renalcis–cement framework. “La Sentinella” is one of the rare examples of Cambrian reef complex displaying community replacement, from an initial stage of thrombolitic and/or flat-stacked microbial crusts on a muddy substrate to an arched microbial crust system, to a more resistant Renalcis–cement boundstone. Such bioherms reflect an open-shelf, shallow-marine environment of increasing energy.
Botoman (Lower Cambrian) turbid- and clear-water reefs and associated environments from the High Atlas, Morocco
Abstract Exposures of the Botoman (Lower Cambrian), Lemdad and Issafen formations on the Lemdad syncline, southern High Atlas, provide an excellent example of the interactions between tectonic events, magmatic activity and carbonate productivity. The major factors that controlled the nucleation of carbonate factories on the Botoman High Atlas platform were: (i) synsedimentary tectonism, as normal faulting resulted in tilting of fault blocks causing irregular topographies and subsequent sharp erosion; (ii) volcanism, because pyroclastic influx smothered carbonate factories except in distal areas of the platform or during quiescent episodes of volcanic activity; and (iii) the influence of successive shoaling parasequences. The Botoman reefs exhibit a wide range of external morphologies, including tabular (biostromes) and domal (bioherms and patches) boundstones, which do not exceed 3.5 m of thickness. Although archaeocyathan–microbial reefs only developed under clear-water conditions, microbial reefs grew also under turbid-water conditions. Domal and digitate stromatoids, Girvanella crusts, Epiphyton bushes and thromboid–stromatoid intergrowths document the ability of some microbial communities to develop heterotrophic strategies when submitted to a moderate terrigenous input. Turbidity was a major ecological factor that constrained development of filter/suspension-feeder and phototrophic organisms, but not necessarily of benthic non-phototrophic microbial communities.
Abstract In the abandoned slate quarry of Guernanic, Gourin (Morbihan, France), a single horizon (Upper Member of the Schistes de Postolonnec Formation) has yielded an exquisitely preserved Llandeilian (Middle Ordovician) echinoderm assemblage composed of the ophiuroid Taeniaster armoricanus sp. nov. and the mitrate Mitrocystella incipiens. These two groups of echinoderms represent the first fossils formally described from the Middle Ordovician of the Gourin area. The brittlestar T. armoricanus sp. nov. is the third and oldest ophiuroid reported so far in the Palaeozoic of the Armorican Massif. The mitrate Mitrocystella is also described for the first time from western Brittany. Taphonomic features of this ophiuroid–stylophoran aggregation suggest that it probably corresponds to the rapid burial of a life assemblage in an otherwise quiet and moderately deep setting (shelf) below, but close to, storm wave base. This echinoderm association represents the oldest evidence for a gregarious mode of life for ophiuroids, as well as the oldest indisputable example of a mixed ophiuroid–stylophoran meadow.
Micritic fabrics define sharp margins of Wenlock patch reefs (middle Silurian) in Gotland and England
Abstract Silurian reefs are well known to comprise frame-building corals, stromatoporoids and algae, but also a range of calcimicrobial components and micritic sediments of possible microbial origin. The margins of Wenlock patch reefs tend to have diffuse edges that grade into the surrounding bedded facies because of talus shed from the reefs. However, portions of patch reefs show sharp-bounded reef margins, with bedded limestones terminating abruptly against the reef edge. Examples of sharp boundaries where the reef comprises only carbonate mudstone–wackestone with poorly-defined gross fabric, and containing no metazoan framework, have been found in Wenlock patch reefs the UK and Gotland. Although in some cases the micrite may demonstrate a peloidal structure, in others there is no clear structure, broadly fitting the aphanitic (structureless) type of fabric found in leiolites (suspected microbial facies that show no structure). The fabrics are interpreted to have been formed by microbial mediation of micrite precipitation as part of reef construction, and are therefore automicrites. In all cases the sharp reef edges indicate coherence of the micritic fabric, interpreted as a lithified wall against which bedded limestones were deposited. This arrangement supports published interpretations of pronounced topography of Wenlock patch reefs, and shows the presence of steep, vertical and, possibly, overhanging reef margins, formed prior to bedded sediment accumulation. Thus, there is likely to have been a time interval between reef formation and deposition of bedded sediments, possibly caused by reef upward growth in transgressive settings, followed by catch-up of bedded limestone deposition.
Abstract Palaeozoic sediments of Austria are separated by the Periadriatic Fault into Eastern Alpine (Upper, Middle and Lower Austroalpine) and Southern Alpine units. We herein present six case studies showing up the different development of shallow-marine communities with special regard to carbonate factories and shell pavements occurring in both regions during the Siluro-Devonian time span. Upper Silurian-Upper Devonian deposits of the Eastern Alps comprise accumulations of serpulid tubes (Southern Burgenland) and Septatrypa pavements, Amphipora mounds, coral-stromatoporoid–biostromes and Stachyodes–auloporoid beds regarded as pioneer reef communities (Graz Palaeozoic), respectively. Lower Silurian strata of the Southern Alps consist of pelagic sediments persisting to the Upper Silurian and therefore differ from contemporaneous successions in the Eastern Alps. Intercalated in Ludlow orthocerid limestone beds Cardiola pavements appear (Carnic Alps). Within the Lower Devonian sequence, mounds were built by baffling calcareous algae and tabulozoan communities. Coral–stromatoporoid patch reefs occur during the Pragian, Givetian and Frasnian stages.