Martin Nose

Microbial crusts of the late jurassic: Composition, palaeoecological significance and importance in reef construction

SummaryUpper Jurassic reefs contain variable amounts of calcareous microbial crusts. In examples from Portugal, Spain and southern Germany they occur within coral biostromes and bioherms, mixed coral-siliceous sponge reefs, siliceous sponge meadows and mudmounds, and build up thrombolities with or without additional reef metazoans. The crusts are of paramount importance for the establishment and development of positive buildups. Commonly, reef growth starts with crusts which develop from a narrow base and rapidly expand laterally by rising above the sea floor. Reef associations with little or no microbial crust normally did not develop distinct relief.The basic microbial crust type is characterised by a dense to peloidal, mostly clotted, hence thrombolitic fabric which developed due to calcification triggered by microbes. Morphological evidence for this organic nature are positive relief, bridge-structures, and the shape and arrangement of peloids. The basic thrombolitic crust type is a eurytopic feature, equally occurring in settings of different bathymetry, waterenergy, salinity and oxygen/nutrient concentrations. However, the crusts also comprise additional micro-encrusters of variable abundance and diversity. The concurrent occurrence of these encrusters and diversity trends allows discrimination between crusts of different environments, particularly of different water depths. Microbial crusts from non-reefal marine oncoids show both similarities and differences with reefal crusts. For some of the mostly enigmatic micro-encrusters new clues to their nature could be detected. For instance, bubble-like structures, formerly interpreted as sporangia inLithocodium could be identified as the foraminiferBullopora aff.laevis, possibly living as a parasite or symbiont in theLithocodium algal tissue.Lithocodium andBacinella are regarded as different organisms.‘Tubiphytes’ morronensis clearly represents a symbiotic intergrowth between a nubeculinellid foraminifer and a microbe of unknown nature.The main prerequisite for the occurrence of microbial crusts is a cessation of background sedimentation which commonly can be tied to rises in sea level. This results in the development of crust-rich reefs. Fluctuations in oxygen and nutrient levels are indicated by dysaerobic bivalves and richness in authigenic glauconite, and led to the microbes outcompeting reefal metazoans, and to the development of thrombolites. Such thrombolites occur at very different depths which is interpreted to be related to a rise of dysaerobic waters due to climatic buffering and lowering of oceanic circulation during sea level rises.Microbial crusts in modern reefs are largely restricted to shaded, cryptic settings which contrasts with the wide distribution of crusts in Upper Jurassic reefs. Microbial crusts were increasingly replaced by coralline red algae since the Late Mesozoic, but despite their restricted modern habitat seem to still play an important, commonly overlooked role in the stabilisation of reef framework.

The origin of Jurassic reefs: Current research developments and results

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

Growth dynamics and ecology of Upper Jurassic mounds, with comparisons to Mid-Palaeozoic mounds

The Mid-Palaeozoic, including the Late Jurassic, was a time of both widespread coral reef growth and pronounced mound formation. A comparison of mound features and their general setting highlights, despite all differences, general similarities in overall growth dynamics. Mound formation was frequently driven by discontinuous patterns, particularly by background sedimentation. In many examples, episodes of mound stabilisation by early lithification, growth of microbolite crusts and winnowing of fines was followed by growth episodes of benthic fauna under reduced to negligible background sedimentation. This pattern of variable sedimentation and organic buildups may have occurred in different orders and magnitudes, inducing a fractal pattern in some mound complexes. A composite approach in estimating growth rates of mounds demonstrates that highfrequency oscillations necessary for growth of most mounds might have ranged from a few thousand years to 4th and 5th order Milankovich cycles that were superimposed by autocyclic factors. D 2001 Elsevier Science B.V. All rights reserved.

The Paleozoic record of Thaumatoporella PIA, 1927?

From Palaeozoic (mainly Devonian) shallow-water carbonates, spherical to irregular shaped microfossils with thin, apparently homogeneous or perforate micritic walls are widely reported. They are classically referred either to unilocular parathuramminid foraminifera, algae incertae sedis or calcispheres (e.g., Bisphaera , Cribrosphaeroides , Uslonia , Vermiporella myna , Irregularina ). Due to their morphology and microstructural features, they are here reassessed more accurately as belonging to Thaumatoporella PIA, a widespread Mesozoic-Early Cenozoic taxon of incertae sedis showing a remarkably high morphological variability. In analogy to Mesozoic thaumatoporellaceans, Bisphaera malevkensis BIRINA is interpreted as the cyst (= resting) stage of forms ascribed to different genera, i.e., Cribrosphaeroides , Uslonia and Vermiporella (here: Vermiporella myna WRAY). This new interpretation leads to taxonomic reassessment as Thaumatoporella malevkensis (BIRINA) nov. comb. As a consequence of our interpretation, the rather long Mesozoic to Early Cenozoic (Ladinian to Early Ypresian) record of thaumatoporellaceans is supposed to be significantly larger than formerly assumed, showing four periods of increased abundance in the Middle/Late Devonian, Late Permian (?), Early/Middle Jurassic and Late Cretaceous time windows.

NEW RECORD OF HALIMEDACEAN ALGAE FROM THE UPPER TRIASSIC OF THE SOUTHERN ALPS (DOLOMITES, ITALY)

A new record of halimedacean algae is reported from the Upper Triassic (Carnian) of the Dolomites (Southern Alps) near Cortina d’Ampezzo. Based on the gross morphology (non-segmented non-branched thalli) and the internal skeletal arrangement (e.g., medulla with thicker siphons, sometimes bifurcating at high angles; cortex with thinner siphons with multiple Y-like branching), the material can be assigned to the genus Boueina . It is the first record of halimedacean algae from the Upper Triassic of the Southern Alps (Dolomites) and the highly diverse San Cassiano Formation sensu lato (Heiligkreuz Formation). Although the fossilization potential of these algae was low, it is likely that they were much more common than suggested by this sparse fossil record and that they contributed considerably to carbonate production in early Mesozoic times.

Ästige tabulate Korallen-Gemeinschaften aus dem Mitteldevon der Sötenicher Mulde (Eifel)

A comparative study of branching tabulate coral-rich successions from the Middle Devonian (lower Givetian) of the