Ankerite

About: Ankerite is a research topic. Over the lifetime, 859 publications have been published within this topic receiving 23960 citations.

Evolution of palaeofluids at the Variscan thrust front in eastern Belgium

Abstract: The geochemical evolution of the fluids migra- ting at the Variscan thrust front in eastern Belgium has been investigated by a petrographic, mineralogical and geoche-mical study of ankerite, quartz and ferroan calcite veins hosted by lower Devonian rocks. Three vein generations have been recognized. The first generation consists of quartz, chlorite and ankerite filling pre- to early Variscan extensional fractures. The second generation is present as shear veins of Variscan age, and contains quartz, chlorite and ferroan calcite. The third generation consists of ankerite filling post-Variscan fractures. The oxygen and carbon isotopic composition of the two ankerite phases and of the ferroan calcites are respectively between –16.4 and –11.4‰ PDB between –17.8 and –1.7‰ PDB. This range is greater than that of calcite nodules in the lower Devonian siliciclastic sediments (δ18O= –15.6 to –11.1‰ PDB and δ13C= –13.4 to –10.2‰ PDB). This suggests precipitation of the carbonate veins from a fluid which was at most only partly isotopically buffered by the calcite nodules in the host rock. The calculated oxygen isotopic composition of the ambient fluid from which the calcite veins formed is between +7.8 and +10.0‰ SMOW. Two main fluid types have been recognized in fluid inclusions in the quartz and carbonates. The first fluid type is present as secondary fluid inclusions in the first and second vein generations. The fluid has a salinity of 0.5–7.2 eq. wt.% NaCl and a high, but variable, homogenization temperature (Th=124–188°C). Two origins can be proposed for this fluid. It could have been expelled from the lower Devonian or could have been derived from the metamorphic zone to the south of the area studied. Taking into account the microthermometric and stable-isotope data, and the regional geological setting, the fluid most likely originated from metamorphic rocks and interacted with the lower Devonian along its migration path. This is in agreement with numerical simulations of the palaeofluid and especially the palaeotempera-ture field, which is based on chlorite geothermometry and vitrinite reflectance data. The second fluid type occurs as secondary inclusions in the shear veins and as fluid inclusions of unknown origin in post-Variscan ankerite veins. Therefore, it has a post-Variscan age. The inclusions are characterized by a high salinity (18.6–22.9 eq. wt.% CaCl2). The composition of the fluid is similar to that which caused the development of Mississippi Valley-type Pb–Zn deposits in Belgium.

Sandstone diagenesis of the Lower Cretaceous Sindong Group, Gyeongsang Basin, southeastern Korea: Implications for compositional and paleoenvironmental controls

Abstract: The Gyeongsang Basin is a non-marine sedimentary basin formed by extensional tectonism during the Early Cretaceous in the southeastern Korean Peninsula. The sediment fill starts with the Sindong Group distributed along the western margin of the basin. It consists of three lithostratigraphic units: the Nakdong (alluvial fan), Hasandong (fluvial) and Jinju (lacustrine) formations with decreasing age. Sindong Group sandstones are classified into four petrofacies (PF) based on their detrital composition: PF-A consists of the lower Nakdong Formation with average Q73F12R15; PF-B the upper Nakdong and lower Hasandong formations with Q66F15R18; PF-C the middle Hasandong to middle Jinju formations with Q49F29R22; and PF-D the upper Jinju Formation with Q26F34R41. The variations of detrital composition influenced the diagenetic mineral assemblage in the Sindong Group sandstones. Illite and dolomite/ankerite are important diagenetic minerals in PF-A and PF-B, whereas calcite and chlorite are dominant diagenetic minerals in PF-C and PF-D. Most of the diagenetic minerals can be divided into early and late diagenetic stages of formation. Early diagenetic calcites occur mostly in PF-C, probably controlled by arid to semiarid climatic conditions during the sandstone deposition, no early calcite being found in PF-A and PF-B. Late-stage calcites are present in all Sindong Group sandstones. The calcium ions may have been derived from shale diagenesis and dissolution of early stage calcites in the Hasandong and Jinju sandstones. Illite, the only diagenetic clay mineral in PF-A and lower PF-B, is inferred to be a product of kaolinite transformation during deep burial, and the former presence of kaolinite is inferred from the humid paleoclimatic conditions during the deposition of the Nakdong Formation. Chlorites in PF-C and PF-D are interpreted to be the products of transformation of smectitic clay or of precipitation from alkaline pore water under arid to semiarid climatic conditions. The occurrence of late-stage diagenetic minerals largely depended on the distribution of early diagenetic minerals, which was controlled initially by the sediment composition and paleoclimate.

Electron microscope analysis of zoned dolomite rhombs in the Jet Rock Formation (Lower Toarcian) of the Whitby area, U.K.

Abstract: Zoned dolomite rhombs which occur in the organic-rich Jet Rock Formation (Toarcian) of northeast England have been studied using backscattered scanning electron microscopy, transmission electron microscopy and energy-dispersive X-ray microanalysis. The rhombs, which are 5–20 μm in size, are variable in chemical composition, but many consist of a dolomite core surrounded by a zone of ferroan dolomite, ankerite or ferroan calcite. Zoned rhombs occur in early-diagenetic calcite-cemented concretions and layers as well as dispersed throughout the shales. Distributional and textural evidence suggests that they formed mainly by primary precipitation from pore fluids within the zone of bacterial sulphate reduction. The ferroan outer zones probably formed after burial below the sulphate reduction zone when insufficient H 2 S was available to react with all the Fe 2+ in solution.

Stable isotope evidence for the origin of diagenetic carbonate minerals from the Lower Jurassic Inmar Formation, southern Israel

Abstract: The oxygen isotope compositions of diagenetic carbonate minerals from the Lower Jurassic Inmar Formation, southern Israel, have been used to identify porewater types during diagenesis. Changes in porewater composition can be related to major geological events within southern Israel. In particular, saline brines played an important role in late (Pliocene-Pleistocene) dolomitization of these rocks. Diagenetic carbonates included early siderite (δ18OSMOW=+24.4 to +26.5‰δ13CPDB=−1.1 to +0.8‰), late dolomite, ferroan dolomite and ankerite (δ18OSMOW=+18.4 to +25.8‰; δ13CPDB=−2.1 to +0.2‰), and calcite (δ18OSMOW=+21.3 to +32.6‰; δ13CPDB=−4.2 to + 3.2‰). The petrographic and isotopic results suggest that siderite formed early in the diagenetic history at shallow depths. The dolomitic phases formed at greater depths late in diagenesis. Crystallization of secondary calcite spans early to late diagenesis, consistent with its large range in isotopic values. A strong negative correlation exists between burial depth (temperature) and the oxygen isotopic compositions of the dolomitic cements. In addition, the δ18O values of the dolomitic phases in the northern Negev and Judea Mountains are in isotopic equilibrium with present formation waters. This behaviour suggests that formation of secondary dolomite post-dates the tectonic activity responsible for the present relief of southern Israel (Upper Miocene to Pliocene) and that the dolomite crystallized from present formation waters. Such is not the case in the Central Negev. In that locality, present formation waters have much lower salinities and δ18O values, indicating invasion of freshwater, and are out of isotopic equilibrium with secondary dolomite. Recharge of the Inmar Formation by meteoric water in the Central Negev occurred in the Pleistocene, and halted formation of dolomite.