| Records |
| Author |
Lima, G.F.C.; Filho, C.A. de C.; Ferreira, V.G.; Lima, J. da S.D.; Marques, E.D.; Minardi, P.S.P.; Dalmázio, I.; Moreira, R.M. |
Title  |
Establishing a water baseline for the unconventional gas industry: A multiple environmental isotopes assessment (18O, 2H, 3H, 13C, and 14C) of surface and groundwater in the São Francisco Basin, Brazil |
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Journal Article |
| Year |
2023 |
Publication |
Applied Geochemistry |
Abbreviated Journal |
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| Volume |
159 |
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105818 |
| Keywords |
Fracking, Groundwater dating, Indaiá river, Isotopes assessment, Shale gas, Unconventional hydrocarbons |
| Abstract |
Unconventional hydrocarbon production has become the target of an intensive environmental debate due to the risks it poses to water resources. Fracking, while enabling the extraction of oil and gas from ultra-low permeability reservoirs, also possesses the risk of polluting water systems through failures from hydraulic fracturing and its associated procedures. The need to foster national industrial development with a transitional energy matrix has led Brazil to discuss the environmental suitability before producing its large unconventional reserves. Many studies have highlighted the need for a robust environmental characterization before the development of the unconventional industry. In this sense, multiple environmental isotopes may work as a proxy for identifying water contamination right from the early stages. Environmental isotopes may also be applied to enhance the understanding of the natural geochemical processes intrinsic to a given area. This study presents an environmental isotopes baseline for the groundwater and riverine water systems within the São Francisco Basin, a proven tight gas reservoir in Brazil, in a pre-operational context. δ18O, δ2H, 3H, δ13C, and Δ14C were evaluated in three different seasons in groundwater and surface water samples, along with other auxiliary parameters such as physical-chemical parameters (in situ), major ions, and d-excess. The δ2H and δ18O in surface water shows an upstream → downstream enrichment trend, with some variations suggesting baseflow interactions in the surface water systems. An evaporation line for the study area was defined as δ2H = 4.6903 δ18O + 10.362. δ13C indicates a mutual dissolution of silicates and carbonates in the groundwater system and suggests a group of samples highly related to the recharge areas. Groundwater dating denotes the Serra da Saudade Formation as a modern fractured aquifer with a strong recharge capacity. These findings support stakeholders in environmental monitoring and management of the unconventional gas industry. |
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0883-2927 |
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THL @ christoph.kuells @ lima_establishing_2023 |
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173 |
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Külls, C.; Marx, V.; Bittner, A.; Ellmies, R.; Seely, M. |
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Environmental impacts on the hydrology of ephemeral streams and alluvial aquifers |
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2009 |
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EGU Geophysical Abstracts |
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5517 |
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THL @ christoph.kuells @ Kuells2009environmental |
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53 |
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Külls, C.; Jobin, J.; Weiler, M. |
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Environmental analytics for water carbon management: enable WCM: Schlussbericht |
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2015 |
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Albert Ludwigs Universität, Professur für Hydrologie |
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THL @ christoph.kuells @ Kuells2015environmental |
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65 |
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Ollivier, C.C.; Carrière, S.D.; Heath, T.; Olioso, A.; Rabefitia, Z.; Rakoto, H.; Oudin, L.; Satgé, F. |
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Ensemble precipitation estimates based on an assessment of 21 gridded precipitation datasets to improve precipitation estimations across Madagascar |
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Journal Article |
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2023 |
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Journal of Hydrology: Regional Studies |
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47 |
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101400 |
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Precipitation products, Remote sensing, Ensemble approach, Hydrology, Madagascar |
| Abstract |
Study region this study focuses on Madagascar. This island is characterized by a great diversity of climate, due to trade winds and the varying topography. This country is also undergoing extreme rainfall events such as droughts and cyclones. Study focus the rain gauge network of Madagascar is limited (about 30 stations). Consequently, we consider relevant satellite-based precipitation datasets to fill gaps in ground-based datasets. We assessed the reliability of 21 satellite-based and reanalysis precipitation products (P-datasets) through a direct comparison with 24 rain gauge station measurements at the monthly time step, using four statistical indicators: Kling-Gupta Efficiency (KGE), Correlation Coefficient (CC), Root Mean Square Error (RMSE), and Bias. Based on this first analysis, we produced a merged dataset based on a weighted average of the 21 products. New hydrological insights for the region based on the KGE and the CC scores, WFDEI (WATCH Forcing Data methodology applied to ERA-Interim), CMORPH-BLD (Climate Prediction Center MORPHing satellite-gauge merged) and MSWEP (Multi-Source Weighted Ensemble Precipitation) are the most accurate for estimating rainfall at the national scale. Additionally, the results reveal a high discrepancy between bio-climatic regions. The merged dataset reveals higher performance than the other products in all situations. These results demonstrate the usefulness of a merging approach in an area with a deficit of rainfall data and a climatic and topographic diversity. |
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2214-5818 |
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THL @ christoph.kuells @ Ollivier2023101400 |
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288 |
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Etschmann, B.; Liu, W.; Li, K.; Dai, S.; Reith, F.; Falconer, D.; Kerr, G.; Paterson, D.; Howard, D.; Kappen, P.; Wykes, J.; Brugger, J. |
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Enrichment of germanium and associated arsenic and tungsten in coal and roll-front uranium deposits |
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Journal Article |
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2017 |
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Chemical Geology |
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463 |
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29-49 |
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Arsenic, Coal, EXAFS and XANES, germanium, Hydrothermal fluids, Metallogenesis, Speciation, Tungsten |
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Most of the World’s germanium (Ge) is mined from Ge-rich lignite, where it is commonly associated with elevated arsenic (As), tungsten (W) and beryllium (Be) contents. Over the past decade, new evidence showing that World-class Ge deposits result from the interaction of hydrothermal fluids with organic matter in coal seams has emerged. Yet, the chemical state of Ge and associated metals in lignite remains poorly understood. We used Mega-pixel Synchrotron X-ray Fluorescence (MSXRF), X-ray Absorption Near Edge Structure (XANES) and Extended X-ray Absorption Fine Structure (EXAFS) to characterize the oxidation states and chemical bonding environment of Ge, As, and W in two world-class Mesozoic Ge-in-lignite deposits (Lincang, Yunnan, southwestern China; Wulantuga, Inner Mongolia, northeastern China); in lignite-bearing uranium (U) ores from the Beverley deposit (South Australia) hosted in Eocene sandstones; and in lignite and preserved wood in late Oligocene-Miocene fluviatile sediments (Gore, Southland, New Zealand). The aim was to improve our understanding of the enrichment mechanism of Ge in lignite and better evaluate the environmental mobility of Ge and some of the associated metals (specifically As and W) in lignite ores. In all samples, chemical maps show that Ge is distributed homogeneously (down to 2μm) within the organic matter. XANES and EXAFS data show that Ge exists in the tetravalent oxidation state and in a distorted octahedral coordination with O, consistent with complexing of Ge by organic ligands. In some pyrite-bearing samples, a minor fraction of Ge is also present as Ge(IV) in association with pyrite. In contrast, As displays a more complex speciation pattern, sometimes even in a single sample, including As(III), As(V), and As(−I/+II) in solid solution in sulfides. Arsenic in sulfides occurs in anionic and cationic forms, i.e., it shows both the common substitution for S22− and the substitution for Fe recently discovered in some hydrothermal pyrites. Tungsten was present as W(VI) in distorted octahedral (3+3) coordination. The EXAFS data confirm the absence or minor contribution of individual W-rich minerals such as scheelite or ferberite to W mass balance in the studied samples. These data show that Ge, W, and probably some As are scavenged via formation of insoluble, oxygen-bridged metal organic complexes in lignite. Destruction of the organic ligands responsible for fixing Ge and W (As) in these lignites is required for liberating the metals, e.g. from waste materials. Geochemical modelling suggests that Ge, W, Be and As all can be extracted from granitic rocks by dilute, low temperature hydrothermal fluids. Germanium is transported mainly as the tetrahedral Ge(OH)4(aq) complex, but fixed as an octahedral oxy-bridged organic complex. The same situation is valid for W, which is transported at the tetrahedral tungstate ion, but most likely scavenged via formation of a 6-coordinated metal-organic species. The Ge-Be-W±As association in Ge-rich coals reflects the source of the metals as well as related scavenging mechanisms. |
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0009-2541 |
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THL @ christoph.kuells @ etschmann_enrichment_2017 |
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183 |
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