3. Electronic Theses and Dissertations (ETDs) - All submissions
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Item Orebody characterisation and structural features that govern copper and cobalt mineralisation in the eastern limb of the Lufilian Arc, Democratic Republic of Congo(2015-02-06) Johnson, Russell DouglasThe Central African Copperbelt is located in the Lufilian Arc which straddles the border between Zambia and the Democratic Republic of Congo (DRC). Mineralisation of the cupriferous Arc is found in basal Neoproterozoic Katangan Supergroup sedimentary rocks, which in DRC are termed the Mines Series Subgroup. The Mines Series is divided into the dolomitic and carbonaceous GRAT, DStrat RSF, RSC, SD and CMN units. The composition of the units is homogeneous across the Lubumbashi district and potentially across the Katangan basin. This study focussed on the Kinsevere and Ruashi deposits in the Lubumbashi district, which are approximately 50 km apart. The study confirmed that relative eustatic sea level changes resulted in the non-deposition of the RSF and RSC stratigraphic units at Kinsevere. Sedimentation was followed by early pervasive potassic alteration and silicification at the diagenetic stage whilst a magnesian dolomitisation event resulted in alteration of potassic feldspars and recrystallisation of carbonates. Albitisation was veincontrolled and late-stage scapolitisation altered evaporitic nodules. Finally, haematisation by late iron-rich fluids circulating through the Roan Group strata resulted in oxidation of sulphides. The structural analysis of Kinsevere Central pit indicates E-W and N-S shortening whereas the Ruashi pit 1 deposit underwent NE-SW and N-S shortening. Initial shortening, associated with Kolwezian deformation (D1), resulted in the formation of NE-thrust folds and a primary set of joints. The Kolwezian deformation event (D2), reoriented the shortening direction from E-W to N-S, creating interference folds and possibly a second set of joints. The final phase in the structural evolution of the Kinsevere and Ruashi deposits was late-stage brittle deformation (faulting). Mineralisation was a multi-stage process. Disseminated chalcopyrite and carrollite were deposited from formation waters during diagenesis in a stable basin environment. Chalcopyrite, carrollite, chalcocite and bornite are predominantly located at the base of the DStrat, whereas chalcopyrite and pyrite dominate the stratigraphically higher portions of the deposits. Hypogene vein mineralisation began at the syn- to late- orogenic stage with carrollite and chalcopyrite in beddingparallel veins. Possible changes in the compression direction created the perpendicularly oriented veins that host chalcopyrite, carrollite, bornite, covellite, digenite and chalcocite. Finally a late stage of chalcopyrite and pyrite deposition occurred in and around the evaporites, indicating a strong correlation between mineralisation, evaporites and scapolitisation. iii Near-surface supergene alteration of hypogene sulphide ores, resulted in Cu-Co carbonates and oxides, such as malachite, azurite, cobaltiferous malachite, chrysocolla, kolwezite and sphaerocobaltite being deposited in vugs and pore spaces above the meteoric water line. Faulted and brecciated zones tend to have deeper supergene alteration. Between the sulphide facies at depth and the supergene oxide facies at surface is a transition zone which marks the depth to which oxidation has penetrated. Sulphur isotope analysis from the Kinsevere and Ruashi deposits suggests a sulphur contribution from a continental Red-Bed sedimentary source and from an evaporitic source.Item The nitrogen and sulfur status and isotopes of soils within the vicinity of a coal-fired power station in South Africa(2013-05-02) Angelova, MiaAmplified loads of sulfate and nitrate have caused increased stress on soil systems in many areas of the world, as both are dominant components of acid rain. This is a critical environmental stress due to the damage caused to soil, water quality and ecosystem functioning. Issues concerning the rising emissions of these elements from local industries have begun to attract increasing attention in South Africa, as the rates of deposition in the Mpumalanga Highveld region alone is comparable to those experienced in First World countries. This study sought to investigate the use of natural stable isotopes of sulfur and nitrogen to identify the process transformations that these species undergo in environmental cycles. Total δ34S, δ15N and δ13C isotope signature of soils in the Mpumalanga region were combined with total elemental concentrations to determine the effect of deposition on the soil system. Soil samples from two soil depths (0 – 10 cm and 20 – 40 cm) were taken along a distance gradient from an identified pollution source, the Majuba power station. Long-term air quality data from the study area were also obtained from Eskom’s air quality monitoring stations, as well as sulfur and nitrogen deposition data from selected literature. Elemental concentrations decreased with soil depth as expected, while sites located approximately 25 km downwind of the power station were seen to contain higher concentrations of both soil sulfur and nitrogen. The mean per site soil sulfur concentration across all depths ranged from 0.009 % to 0.048 %, while the mean per site nitrogen concentration across all depths ranged from 0.056 % to 0.346 %. The mean soil carbon concentration in the top-soils ranged from 0.97 % to 7.93 %, and decreased in the sub-soils to 0.490 % to 3.270 %.The mean δ34S value for the top-soils was found to be 8.28 ‰ and increased to 10.78 ‰ in the sub-soils. Soil δ15N also increased with soil depth from 6.55 ‰ to 8.28 ‰. Soil δ13C values were seen to increase from -12.83 ‰ in the top-soils to -11.90 ‰ in the sub-soils. Lighter δ34S values at the surface may be due to anthropogenic deposition. The positive δ34S shift was attributed to a two-source mixing model (atmospheric deposition and bedrock) and isotopic fractionation processes that occur within the soil profile. The δ15N values of the top-soil were higher than what is expected if all nitrogen was derived from atmospheric nitrogen gas fixation. The increase in δ15N with depth suggested that isotope fractionation occurred during nitrogen export due to the faster reaction rate of 14N compared to 15N. The soil δ13C values indicated a typical C4 grassland system. New carbon at the top-soil depths was enriched in 13C due to the slower decay of 13C-depleted lignin; whereas in the sub-soils microbial recycling of carbon dominates and explained the higher 13C content of the older carbon. The conceptual framework presented for this project involves simultaneous processes of deposition and export in the soil system. This was particularly true for sulfur, where sites with lower isotope values had lower soil sulfur concentrations and vice versa. This indicates that high levels of deposition correspond to high net export. The sulfur and nitrogen isotopic signatures could not be used to as a direct means of source identification; however, the effectiveness of isotopes in elucidating transfer of these nutrients in the soil system was illustrated.