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Observations on the origin of micrite crystals
Institution:1. Key Laboratory of Carbonate Reservoirs, China National Petroleum Corporation, Hangzhou 310023, China;2. PetroChina Hangzhou Research Institute of Geology, Hangzhou 310023, China;1. Norwegian Geotechnical Institute, Level 7, 40 St Georges Terrace, Perth, WA 6000, Australia;2. Centre for Energy and Climate Geoscience, School of Earth Sciences, The University of Western Australia, 35 Stirling Highway, Perth, WA 6009, Australia;3. UWA Oceans Institute, The University of Western Australia, Perth, WA 6009, Australia;4. School of Geosciences, The University of Sydney, NSW 2006, Australia;1. Aix-Marseille Université, CNRS, IRD, Cerege, Um 34, 3 Place Victor Hugo (Case 67), 13331 Marseille Cedex 03, France;2. VU University Amsterdam, Faculty of Earth and Life Sciences (FALW), Department of Sedimentology and Marine Geology, De Boelelaan 1085, 1081 HV Amsterdam, The Netherlands
Abstract:The transformation of depositional lime mud to microporous micrite has been the subject of several important papers recently in response to the recognition that micropores are important to the production of carbonate hydrocarbon reservoirs. The origin of micrite has generally been described as a micro dissolution and reprecipitation process (often referred to as Ostwald ripening), with nanometer-sized depositional particles being dissolved and larger crystals (micrite) averaging 2 μm in diameter being precipitated. These conclusions were tested by detailed scanning electron microscope (SEM) observations of micrite and minimicrite crystals found in the mid-Pliocene to upper Miocene section of the Clino core taken on the western edge of the Bahama Bank. Minimicrite in this data set is shown to be composed of both aragonite and calcite with calcite being the dominate mineral. In addition, micrite crystals are composed of cemented nanometer-sized calcite crystals and are not individually precipitated calcite crystals. As a result, the faces of the micrite are anhedral and knobby in appearance rather than being smooth, euhedral crystal faces. Extensive size measurements could find no size selectivity in the dissolution of the calcite minimicrite, indicating that the Ostwald ripening process is not active. Aragonite and calcite crystals are dissolved and some calcite crystals act as nuclei for the precipitation of the dissolved carbonate. The origin of the micropores is also debated. Some authors call upon a dissolution event to increase porosity of a partially cemented micrite, based largely on the anhedral nature of the micrite. Others conclude that porosity is originally inherited from the deposition lime mud and that porosity is lost by overgrowth cementation, which results in euhedral micrite crystals. The observations presented here show that anhedral crystals are due to the inclusion of nanometer calcite crystals rather than to dissolution of euhedral crystals. Lastly, these micrite crystals are formed by calcite and aragonite sediment precipitated from an aragonitic sea, disproving the assertion of some authors that porous micrite only forms from sediments deposited in calcitic seas.
Keywords:Micrite  Carbonate  Transformation  Ostwald ripening  Micrite crystal morphology
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