Over the last decade, our studies in ancient evaporitic basins have been based on a detailed study of a single borehole record. The detailed findings in medium- to large-sized evaporitic basins were shadowed with a relevant question: can interpretations from a representative evaporitic record in a single borehole be extended to the whole evaporitic basin? This paper addresses that question; the results obtained are compared with results from another distant point within the basin. The general methodology not only proves its reliability in interpreting the evolution of evaporitic basins from a single borehole but reveals its capability to obtain detailed palaeoenvironmental interpretations.
The chemical evolution of an Upper Eocene evaporitic sequence from the South Pyrenean foreland basin (Spain) has been investigated along the Súria-19 borehole record. Detailed petrographic and mineralogical study, X-ray microanalysis of frozen primary inclusions trapped in halite (Cryo-SEM-EDS), systematic isotopic analysis (δ34S and δ18O in sulphates) and computer-based evaporation models have been integrated in a multi-proxy methodology. This study revealed that a variable amount of Ca excess is required throughout different parts of the marine Lower Halite Unit (LHU) for sylvite, instead of K–Mg sulphates, to form. This Ca excess is in turn different from that required for the western sector of the same evaporitic basin (Navarrese subbasin). Quick and variable changes in Ca-rich brines or equivalent dolomitization required are explained as internal processes within the basin rather than secular variations in seawater chemistry.
The general hydrological evolution of the Catalan subbasin is explained as a restricted subbasin with a first marine stage in which continental input (up to 50% of total input) had an important control on the geochemistry of the subbasin. A second stage was determined during potash precipitation, in which the subbasin was cut from any seawater input to end up in its last stage as a purely continental evaporitic basin. Coupling evaporation models and analytical results we have obtained the proportions of recycling and their sources, estimated to change from a 100% (total mass of sulphate) Eocene source to 20% Eocene and 80% Triassic (Keuper) towards the latest stage of potash precipitation. The results obtained have been compared with results from the Navarrese subbasin allowing an integrated interpretation of the hydrological evolution of the whole Upper Eocene South Pyrenean basin. Local geochemical variations within the Upper Eocene south Pyrenean basin are explained by the differences in paleogeographical setting of the Navarrese and Catalan subbasins. 相似文献
Anaerobic biodegradation of hydrocarbons, using a variety of terminal electron acceptors (TEAs), is increasingly being reported both in laboratory studies and in the field. Of all the petroleum hydrocarbons, benzene is considered the most problematical due to its high toxicity and relatively high aqueous solubility. These, combined with its peculiarly stable structure, mean that it has long been considered recalcitrant in all but aerobic conditions. There is now a small, but growing, literature to suggest that this may not in fact be the case. We present an assessment of the field, encompassing reviews up to 1997 and original papers published since then. It appears that benzene is indeed degraded anaerobically, but that organisms capable of doing so are not ubiquitous. In addition, benzene degradation may be competitively inhibited by the presence of more readily degraded compounds such as toluene. Certainly, the occurrence and rate of benzene attenuation under anaerobic conditions is far more site-specific than for other benzene, toluene, ethylbenzene and xylenes (BTEX) compounds. We discuss a mathematical method for modelling redox-dependent, differential degradation rates. 相似文献
Gold extraction at the Macraes gold mine in New Zealand involves concentration of pyrite and arsenopyrite, oxidation of those sulphides, then cyanidation. The ore concentrate is predominantly Otago Schist host rock (andesitic composition) with up to 15% sulphides. The oxidation step is conducted on ore concentrate slurry in an autoclave at 225°C and 3,800 kPa oxygen gas pressure with continuous feed. The slurry takes ca. 1 h to pass through the autoclave, during which time the sulphides are almost completely oxidised. Sulphide oxidation causes strong acidification of the slurry, which is maintained at pH of 1–2 by addition of CaCO3. Scales form on walls in the autoclave, with minerals reflecting progressive oxidation and alteration of the ore through the system. The schist in the ore feed has mineralogy similar to propylitically altered andesite: quartz, albite, muscovite, chlorite, and pyrite. Muscovite undergoes almost complete dissolution, with associated precipitation of quartz and alunite (KAl3(SO4)2(OH)6). Other principal minerals deposited and discharged include anhydrite (and/or gypsum), jarosite (KFe3(SO4)2(OH)6), hematite (and/or amorphous iron oxyhydroxide), and amorphous arsenates. Dissolved ferrous iron passes right through the autoclave, and variably hydrated Fe2+and Fe3+sulphate minerals, including rozenite and szomolnokite (both FeSO4.hydrate) and ferricopiapite (Fe5(SO4)6O(OH).hydrate), are formed along the way. The autoclave chemical system resembles acid–sulphate hydrothermal activity in geothermal systems and high-sulphidation epithermal mineral deposits formed in arc environments. These natural acid–sulphate systems are pervaded by volcanic vapours in the near-surface environment, where widespread dissolution of host rocks occurs and deposition of quartz, alunite, and anhydrite is common. Some of the volume loss associated with these natural systems may be due to dissolution of soluble sulphate minerals by later-stage groundwater incursion. 相似文献
During March and April of 1995 a major international field project was conducted at the UMIST field station site on Great Dun Fell in Cumbria, Northern England. The hill cap cloud which frequently envelopes this site was used as a natural flow through reactor to examine the sensitivity of the cloud microphysics to the aerosol entering the cloud and also to investigate the effects of the cloud in changing the aerosol size distribution, chemical composition and associated optical properties. To investigate these processes, detailed measurements of the cloud water chemistry (including the chemistry of sulphur compounds, organic and inorganic oxidised nitrogen and ammonia), cloud microphysics and properties of the aerosol and trace gas concentrations upwind and downwind of the cap cloud were undertaken. It was found that the cloud droplet number was generally strongly correlated to aerosol number concentration, with up to 2000 activated droplets cm−3 being observed in the most polluted conditions. In such conditions it was inferred that hygroscopic organic compounds were important in the activation process. Often, the size distribution of the aerosol was substantially modified by the cloud processing, largely due to the aqueous phase oxidation of S(IV) to sulphate by hydrogen peroxide, but also through the uptake and fixing of gas phase nitric acid as nitrate, increasing the calculated optical scattering of the aerosol substantially (by up to 24%). New particle formation was also observed in the ultrafine aerosol mode (at about 5 nm) downwind of the cap cloud, particularly in conditions of low total aerosol surface area and in the presence of ammonia and HCl gases. This was seen to occur at night as well as during the day via a mechanism which is not yet understood. The implications of these results for parameterising aerosol growth in Global Climate Models are explored. 相似文献
