Abstract

Several diagenetic models have been proposed for Middle and Upper Jurassic carbonates of the eastern Paris Basin. The paragenetic sequences are compared in both aquifers to propose a diagenetic model for the Middle and Late Jurassic deposits as a whole. Petrographic (optical and cathodoluminescence microscopy), structural (fracture orientations) and geochemical (δ18O, δ13C, REE) studies were conducted to characterize diagenetic cements, with a focus on blocky calcite cements, and their connection with fracturation events. Four generations of blocky calcite (Cal1–Cal4) are identified. Cal1 and Cal2 are widespread in the dominantly grain-supported facies of the Middle Jurassic limestones (about 90% of the cementation), whereas they are limited in the Oxfordian because grain-supported facies are restricted to certain stratigraphic levels. Cal1 and Cal2 blocky spars precipitated during burial in a reducing environment from mixed marine-meteoric waters and/or buffered meteoric waters. The meteoric waters probably entered aquifers during the Late Cimmerian (Jurassic/Cretaceous boundary) and Late Aptian (Early Cretaceous) unconformities. The amount of Cal2 cement is thought to be linked to the intensity of burial pressure dissolution, which in turn was partly controlled by the clay content of the host rocks. Cal3 and Cal4 are associated with telogenetic fracturing phases. The succession of Cal3 and Cal4 calcite relates to the transition towards oxidizing conditions during an opening of the system to meteoric waters at higher water/rock ratios. These meteoric fluids circulated along Pyrenean, Oligocene and Alpine fractures and generated both dissolution and subsequent cementation in Oxfordian vugs in mud-supported facies and in poorly stylolitized grainstones. However, these cements filled only the residual porosity in Middle Jurassic limestones. In addition to fluorine inputs, fracturation also permitted inputs of sulphur possibly due to weathering of Triassic or Purbeckian evaporites or H2S input during Paleogene times.

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