1. The origin of celestine–quartz–calcite geodes associated with a basaltic dyke, Makhtesh Ramon, Israel.
- Author
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ANENBURG, MICHAEL, BIALIK, OR M., VAPNIK, YEVGENY, CHAPMAN, HAZEL J., ANTLER, GILAD, KATZIR, YARON, and BICKLE, MIKE J.
- Subjects
CELESTITE ,CALCITE ,GEODES ,SULFATE minerals - Abstract
Spectacular celestine geodes occur in a Jurassic peri-evaporitic sequence (Ardon Formation) exposed in Makhtesh Ramon, southern Israel. The geodes are found only in one specific location: adjacent to an intrusive contact with a Lower Cretaceous basaltic dyke. Celestine, well known in sedimentary associations worldwide and considered as a low temperature mineral, may therefore be associated with magmatic-induced hydrothermal activity. Abundant fluid inclusions in celestine provide valuable information on its origin: gas-rich inclusions in celestine interiors homogenized at T≥200°C whereas smaller liquid-rich inclusions record the growth of celestine rims at T≤200°C. Near 0°C melting temperatures of some fluid inclusions and the occurrence of hydrous Ca-sulphate solid crystals in other inclusions indicate that celestine precipitated from variably concentrated Ca-sulphate aqueous solutions of meteoric origin. Celestine crystallized from meteoric water heated by the cooling basaltic dyke at shallow levels (c. 160 m) during a Lower Cretaceous thermal perturbation recorded by regional uplift and magmatism. The 87Sr/86Sr ratio of geode celestine, 0.7074, is similar to that measured in the dolostones of the host Jurassic sequence, but differs markedly from the non-radiogenic ratio of the dyke. Strontium in celestine was derived from dolostones preserving the 87Sr/86Sr of Lower Jurassic seawater, while sulphur (δ34S = 19.9‰) was provided by in situ dissolution of precursor marine gypsum (δ34S = 16.8‰) indicated by relict anhydrite inclusions in celestine. Low-temperature meteoric fluid flow during the Campanian caused alteration of the dyke into secondary clays and alteration of geodal celestine into quartz, calcite and iron oxides. [ABSTRACT FROM AUTHOR]
- Published
- 2014
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