Hall, Gwendy E.M
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Hall, Gwendy E.M
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Hall, Gwendy E.M
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Hall, G. E. M.
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Item-typ:Veröffentlichung, The chemical composition of shallow-water hydrothermal fluids in Tutum Bay, Ambitle Island, Papua New Guinea and their effect on ambient seawaterSubmarine, hydrothermal venting occurs at Tutum Bay in shallow (5–10 m) water along the inner shelf that contains a patchy distribution of coral–algal reefs. Two types of venting are observed. (1) Focused discharge of a clear, two-phase fluid from discrete orifices, 10–15 cm in diameter. Discharge temperatures are between 89 and 98°C and estimated flow rates are as high as 300 to 400 l/min. (2) Dispersed or diffuse discharge that consists of streams of gas bubbles ubiquitous in the area. The composition of the gas is mainly CO2 (92.6–97.9%) with minor amounts of N2 (2.2–4.7%), O2 (0.43–0.73%), CH4 (0.6–2%) and He (∼0.01–0.02%). Based on their geographic position and chemical composition, the vents have been divided into two groups, A and B. Area B vents have higher K, Rb, Sb, Cs, Tl, and As and lower Ca, Li, Mn, Fe, and Sr concentrations. Their chemical difference is likely caused by subsurface mixing of a CO2-rich water with a deep reservoir neutral chloride fluid in varying proportions. A two- or possibly three-step process controls fluid evolution and final chemical composition: (1) phase separation in the deep reservoir beneath Ambitle Island produces a high temperature vapor that rises upward and subsequently reacts with cooler ground water to form a low pH, CO2-rich water of approximately 150–160°C. (2) The steep topography causes lateral movement of this CO2-rich fluid towards the margin of the hydrothermal system where it mixes with the marginal upflow from the deep reservoir. This produces a dilute chloride water of approximately 165°C. A third step may be the entrainment of minor amounts of ground or seawater during its final ascent. Based on a B–Rb/Cs mixing model, it has been estimated that approximately 10% of the deep reservoir fluid reaches the surface. Compared to seawater, the hydrothermal fluids are depleted in Cl, Br, SO4, Na, K, Ca, Mg, and Sr and enriched in HCO3, B, Si, Li, Mn, Fe, Rb, Cs, Sb, Tl and As. Although some elements are significantly enriched, they do not have a clear impact on ambient seawater composition because their concentration is buffered by mixing and uptake into secondary minerals. Only the surface water in Tutum Bay carries a clear imprint of the hydrothermal fluids.Wissenschaftlicher ArtikelBand:64Heft:387 71 - Some of the metrics are blocked by yourconsent settings
Item-typ:Veröffentlichung, The mineralogy of arsenic in uranium mine tailings at the Rabbit Lake In-pit Facility, northern Saskatchewan, CanadaA detailed investigation of the mineralogy of As in the tailings of the Rabbit Lake uranium ore processing facility was conducted. The milling/ore extraction process was sampled at three different locations to obtain information about when, where and under what condition secondary As phases form. These samples were compared with four samples of varying As content from the Rabbit Lake in-pit tailings management facility (TMF). Up to 20% As in the tailings are present in primary minerals that reach the tailings directly because they are not dissolved during the uranium extraction. The remaining 80% constitute As that was dissolved during ore extraction and then re-precipitated before being discharged into the tailings pond. It was not possible to conclusively identify any individual re-precipitated (secondary) As minerals in the Rabbit Lake TMF. Indirect evidence from sequential extraction analyses suggests the presence of an amorphous Ca-As phase and a possible, but unlikely, minor amount of an amorphous Fe-As phase. However, the close association between hydrous ferric oxide (HFO) and As could be clearly demonstrated. HFO was identified to be 2-line ferrihydrite and its XRD pattern geometry indicates a substantial amount of adsorbed As. This is in good agreement with SEM, TEM and sequential extraction analyses that all showed the close association of HFO and As.Wissenschaftlicher ArtikelBand:4063 57