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A composite Tethyan Late Jurassic–Early Cretaceous carbon and oxygen isotope curve is presented. C-isotope data provide information on the evolution and perturbation of the global carbon cycle. O-isotope data are used as a palaeotemperature proxy in combination with palaeontological information. The resulting trends in climate and in palaeoceanography are compared with biocalcification trends and oceanographic conditions favouring or inhibiting biocalcification. Positive C-isotope anomalies in the Valanginian and Aptian correlate with episodes of increased volcanic activity regarded as a source of excess atmospheric carbon dioxide. A major warming pulse accompanies the Aptian but not the Valanginian C-isotope event. The observed change in Early Aptian temperatures could have triggered the destabilization of sedimentary gas hydrates and the sudden release of methane to the biosphere as recorded as a distinct negative carbon isotope pulse preceding the positive excursion. Both C-isotope anomalies are accompanied by biocalcification crises that may have been triggered by p CO 2 -induced changes in climate and in surface water chemistry. Elevated nutrient levels in river-influenced coastal waters and in upwelling regions further weakened marine calcification. These conditions contrast with ‘normal’ trophic conditions prevailing in the latest Jurassic and favouring biocalcification. The C- and O-isotope curves record a stable mode of carbon cycling and stable temperatures. We conclude that biocalcification is mostly triggered (and inhibited) by CO 2 conditions in the atmosphere–ocean system.

Ocean acidification induced by atmospheric CO2 may be a major threat to marine ecosystems, particularly to calcareous nannoplankton. We show that, during the Aptian (approximately 120 million years ago) Oceanic Anoxic Event 1a, which resulted from a massive addition of volcanic CO2, the morphological features of calcareous nannofossils traced the biological response to acidified surface waters. We observe the demise of heavily calcified nannoconids and reduced calcite paleofluxes at the beginning of a pre-anoxia calcification crisis. Ephemeral coccolith dwarfism and malformation represent species-specific adjustments to survive lower pH, whereas later, abundance peaks indicate intermittent alkalinity recovery. Deepwater acidification occurred with a delay of 25,000 to 30,000 years. After the dissolution climax, nannoplankton and carbonate recovery developed over approximately 160,000 years under persisting global dysoxia-anoxia.

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