Abstract:The key objective of investigation of hemipelagic sediments from the Gresten Klippenbelt (Blassenstein Formation, Ultrahelvetic paleogeographic realm) was to shed light on environmental changes around the Jurassic-Cretaceous (J/K) boundary on the northern margin of the Penninic Ocean. This boundary is well exposed in a newly discovered site at Nutzhof. Around the critical interval including the boundary, this new outcrop bears a rich microplanktonic assemblage characterized by typical J/K (Tithonian/Berriasian) boundary faunas. The Nutzhof section is located in the Gresten Klippenbelt (Lower Austria) tectonically wedged into the deep-water sediments of the Rhenodanubian Flysch Zone. In Late JurassicEarly Cretaceous time the Penninic Ocean was a side tract of the proto-North Atlantic Oceanic System, intercalated between the European and the Austroalpine plates. Its opening started during the Early Jurassic, induced by sea floor spreading, followed by Jurassic-Early Cretaceous deepening of the depositional area of the Gresten Klippenbelt. These tectonically induced paleogeographic changes are mirrored in the lithology and microfauna that record a deepening of the depositional environment from Tithonian to Berriasian sediments of the Blassenstein Formation at Nutzhof. The main lithological change is observed in the Upper Tithonian Crassicollaria Zone, in Chron M20N, whereas the J/K boundary can be precisely fixed at the Crassicollaria-Calpionella boundary, within Chron M19n.2n. The lithological turnover of the deposition from more siliciclastic pelagic marl-limestone cycles into deep-water pelagic limestones is correlated with the deepening of the southern edge of the European continent at this time. Within the Gresten Klippenbelt Unit, this transition is reflected by the lithostratigraphic boundary between siliciclastic-bearing marl-limestone sedimentation in the uppermost Jurassic and lowermost Cretaceous limestone formation, both within the Blassenstein Formation. The cephalopod fauna (ammonites, belemnites, aptychi) and crinoids from the Blassenstein Formation, correlated with calcareous microfossil and nannofossil data combined with isotope and paleomagnetic data, indicate the Tithonian to middle Berriasian (Hybonoticeras hybonotum Zone up to the Subthurmannia occitanica Zone; M17r-M21r). The succession of the Nutzhof section thus represents deposition of a duration of approximately 7 . The deposition of the limestone, marly limestone and marls in this interval occurred during tectonically unstable conditions reflected by common allodapic material. Along with the integrated biostratigraphic, geochemical and isotopic analysis, the susceptibility and gamma-ray measurements were powerful stratigraphic tools and important for the interpretation of the paleogeographic setting. Two reverse magneto-subzones, Kysuca and Brodno, were detected within magnetozones M20n and M19n, respectively.

In contrast to the Palaeozoic to Jurassic fossil record, modern tropical and subtropical shallow-water brachiopods are typically small-sized and mostly restricted to cryptic habitats in coral reefs, but information on microhabitat-composition is scant. At Dahab, northern Red Sea, living brachiopods of the genus Argyrotheca were only detected on massively encrusted coral colonies attached to encrusting foraminifers and coralline red algae. Three samples from autochthonous sediments underneath coral colonies are comparatively rich in the brachiopod genera Megerlia and Argyrotheca, and additionally show low numbers of Novocrania and Thecidellina. Based on a coarse-grain analysis including more than 16,000 components >1 mm, these brachiopod shells co-occur with skeletal components of 11 higher taxa. Decapods, Wxosessile foraminifers, molluscs, scleractinians, and coralline red algae clearly dominate the assemblages. Brachiopods in this study always contribute less than 2% to the sediment composition. This conWrms previous results that even in brachiopod habitats the contribution of brachiopod shells to the total sediment composition is almost negligible. Our study indicates that brachiopods co-occur with pteriomorph bivalves and other epifauna in the cryptic habitats with limited space for encrusters or epibionts on the undersides of scleractinians and it tentatively supports the hypothesis of brachiopods preferring habitats with low grazing pressure, because shelly components of grazers (polyplacophorans and regular echinoids) are rare in our samples.

A Julian/Tuvalian (¼Lower/Upper Carnian) substage boundary within the Kasımlar Formation, recently detected at Aşagiyaylabel (Taurus Mountains, Turkey) by facies analyses and biostratigraphic ammonoid investigations, was additionally detected by magnetic susceptibility (MS) and radiometry data. The Aşagiyaylabel sequence, a key section concerning environmental changes during Early to Late Carnian time, represents a deepening sequence from platform carbonates to pelagic limestones and marls. The Julian/Tuvalian boundary strata can be correlated over wide areas due to a positive shift in MS values from 11-105 × 10 26 SI (range AS

The deposits of the Carnian Kasımlar Formation within the Taurus Platform Units of south‐western Turkey represent an important archive of a Late Triassic ecosystem. New palaeontological information was obtained by analysing the Kasimlarceltites mass occurrence, located within the Kasımlar Formation and named after the Lower Carnian (Julian) ammonoid genus Kasimlarceltites. This is the dominant taxon (> 94%) within the mass occurrence: nearly 775 million ammonoids and 50 million gastropods were extrapolated for the whole extension (at least 5 km2) of the Kasimlarceltites beds. This calculation is one of the main findings within this study, as it is the first time that such a fossil mass occurrence was quantified. Additionally, orientation measurements of the planispiral ammonoids and the helical gastropods enabled reconstructing the history of the mass occurrence and interpreting the underlying transport mechanisms. Further taphonomic aspects (e.g. biofabric, preservation, bioerosion or genetic classification) as well as comparisons with samples of the same acme zone from different localities near Aşağiyaylabel (AS IV, KA I‐II) point to a two‐phased genetic history. Accordingly, local mass mortality within the Kasimlarceltites fauna due to oxygen fluctuations or methane degassing may have initially led to a primary accumulation. These deposits were then reworked and redeposited basinward by gravity flows to create the present‐day secondary allochthonous concentrations.

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