Records |
Author |
Dutova, E.M.; Nikitenkov, A.N.; Pokrovskiy, V.D.; Banks, D.; Frengstad, B.S.; Parnachev, V.P. |
Title |
Modelling of the dissolution and reprecipitation of uranium under oxidising conditions in the zone of shallow groundwater circulation |
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Journal Article |
Year |
2017 |
Publication |
Journal of Environmental Radioactivity |
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Volume |
178-179 |
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Pages |
63-76 |
Keywords |
Groundwater, Hydrochemical modelling, Mineralisation, Natural uranium, Ore, Solubility |
Abstract |
Generic hydrochemical modelling of a grantoid-groundwater system, using the Russian software “HydroGeo”, has been carried out with an emphasis on simulating the accumulation of uranium in the aqueous phase. The baseline model run simulates shallow granitoid aquifers (U content 5 ppm) under conditions broadly representative of southern Norway and southwestern Siberia: i.e. temperature 10 °C, equilibrated with a soil gas partial CO2 pressure (PCO2, open system) of 10−2.5 atm. and a mildly oxidising redox environment (Eh = +50 mV). Modelling indicates that aqueous uranium accumulates in parallel with total dissolved solids (or groundwater mineralisation M – regarded as an indicator of degree of hydrochemical evolution), accumulating most rapidly when M = 550–1000 mg L−1. Accumulation slows at the onset of saturation and precipitation of secondary uranium minerals at M = c. 1000 mg L−1 (which, under baseline modelling conditions, also corresponds approximately to calcite saturation and transition to Na-HCO3 hydrofacies). The secondary minerals are typically “black” uranium oxides of mixed oxidation state (e.g. U3O7 and U4O9). For rock U content of 5–50 ppm, it is possible to generate a wide variety of aqueous uranium concentrations, up to a maximum of just over 1 mg L−1, but with typical concentrations of up to 10 μg L−1 for modest degrees of hydrochemical maturity (as indicated by M). These observations correspond extremely well with real groundwater analyses from the Altai-Sayan region of Russia and Norwegian crystalline bedrock aquifers. The timing (with respect to M) and degree of aqueous uranium accumulation are also sensitive to Eh (greater mobilisation at higher Eh), uranium content of rocks (aqueous concentration increases as rock content increases) and PCO2 (low PCO2 favours higher pH, rapid accumulation of aqueous U and earlier saturation with respect to uranium minerals). |
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0265-931x |
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THL @ christoph.kuells @ dutova_modelling_2017 |
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114 |
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Post, V.E.A.; Vassolo, S.I.; Tiberghien, C.; Baranyikwa, D.; Miburo, D. |
Title |
Weathering and evaporation controls on dissolved uranium concentrations in groundwater – A case study from northern Burundi |
Type |
Journal Article |
Year |
2017 |
Publication |
Science of The Total Environment |
Abbreviated Journal |
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Volume |
607-608 |
Issue |
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Pages |
281-293 |
Keywords |
Geochemical modelling, Hydrochemistry, Lake Tshohoha South, Public health, Radionuclides, Water supply |
Abstract |
The potential use of groundwater for potable water supply can be severely compromised by natural contaminants such as uranium. The environmental mobility of uranium depends on a suite of factors including aquifer lithology, redox conditions, complexing agents, and hydrological processes. Uranium concentrations of up to 734μg/L are found in groundwater in northern Burundi, and the objective of the present study was to identify the causes for these elevated concentrations. Based on a comprehensive data set of groundwater chemistry, geology, and hydrological measurements, it was found that the highest dissolved uranium concentrations in groundwater occur near the shores of Lake Tshohoha South and other smaller lakes nearby. A model is proposed in which weathering and evapotranspiration during groundwater recharge, flow and discharge exert the dominant controls on the groundwater chemical composition. Results of PHREEQC simulations quantitatively confirm this conceptual model and show that uranium mobilization followed by evapo-concentration is the most likely explanation for the high dissolved uranium concentrations observed. The uranium source is the granitic sand, which was found to have a mean elemental uranium content of 14ppm, but the exact mobilization process could not be established. Uranium concentrations may further be controlled by adsorption, especially where calcium-uranyl‑carbonate complexes are present. Water and uranium mass balance calculations for Lake Tshohoha South are consistent with the inferred fluxes and show that high‑uranium groundwater represents only a minor fraction of the overall water input to the lake. These findings highlight that the evaporation effects that cause radionuclide concentrations to rise to harmful levels in groundwater discharge areas are not only confined to arid regions, and that this should be considered when selecting suitable locations for water supply wells. |
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0048-9697 |
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THL @ christoph.kuells @ post_weathering_2017 |
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132 |
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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. |
Title |
Enrichment of germanium and associated arsenic and tungsten in coal and roll-front uranium deposits |
Type |
Journal Article |
Year |
2017 |
Publication |
Chemical Geology |
Abbreviated Journal |
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Volume |
463 |
Issue |
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Pages |
29-49 |
Keywords |
Arsenic, Coal, EXAFS and XANES, germanium, Hydrothermal fluids, Metallogenesis, Speciation, Tungsten |
Abstract |
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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Author |
Bullock, L.A.; Parnell, J. |
Title |
Selenium and molybdenum enrichment in uranium roll-front deposits of Wyoming and Colorado, USA |
Type |
Journal Article |
Year |
2017 |
Publication |
Journal of Geochemical Exploration |
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Volume |
180 |
Issue |
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Pages |
101-112 |
Keywords |
Molybdenum, Roll-fronts, Selenium, Tellurium, Uranium, Wyoming |
Abstract |
Sandstone uranium (U) roll-front deposits of Wyoming and Colorado (USA) are important U resources, and may provide a terrestrial source for critical accessory elements, such as selenium (Se), molybdenum (Mo), and tellurium (Te). Due to their associated toxicity, MoSeTe occurrences in roll-fronts should also be carefully monitored during U leaching and ore processing. While elevated MoSe concentrations in roll-fronts are well established, very little is known about Te occurrence in such deposits. This study aims to establish MoSeTe concentrations in Wyoming and Colorado roll-fronts, and assess the significance of these deposits in an environmental and mineral exploration context. Sampled roll-front deposits, produced by oxidized groundwater transportation through a sandstone, show high MoSe content in specific redox zones, and low Te, relative to crustal means. High Se concentrations (up to 168ppm) are restricted to a narrow band of alteration at the redox front. High Mo content (up to 115ppm) is typically associated with the reduced mineralized nose and seepage zones of the roll-front, ahead of the U orebody. Elevated trace element concentrations are likely sourced from proximal granitic intrusions, tuffaceous deposits, and local pyritic mudstones. Elevated MoSe content in the sampled roll fronts may be regarded as a contaminant in U in-situ recovery and leaching processing, and may pose an environmental threat in groundwaters and soils, so extraction should be carefully monitored. The identification of peak concentrations of MoSe can also act as a pathfinder for the redox front of a roll-front, and help to isolate the U orebody, particularly in the absence of gamma signatures. |
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0375-6742 |
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THL @ christoph.kuells @ bullock_selenium_2017 |
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189 |
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Author |
Brutsaert, W. |
Title |
Global land surface evaporation trend during the past half century: Corroboration by Clausius-Clapeyron scaling |
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Journal Article |
Year |
2017 |
Publication |
Advances in Water Resources |
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106 |
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3-5 |
Keywords |
Evaporation, Climate change, Evaporation trend |
Abstract |
Analyses of satellite data mainly over the world’s ocean surfaces have shown that during 1986–2006 global average values of atmospheric water vapor, precipitation and evaporation have increased at a relative rate of 0.0013a−1; this is roughly in accordance with the Clausius-Clapeyron equation for the average temperature trend during this period, and amounts to 0.065K−1 at the average temperature of T=14∘C. Application of this concept over the world’s land surfaces yields an average global evaporation trend during the past half century of around 0.4 to 0.5 mma−2; this confirms the values obtained in previous studies with totally different methods. |
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0309-1708 |
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Tribute to Professor Garrison Sposito: An Exceptional Hydrologist and Geochemist |
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THL @ christoph.kuells @ Brutsaert20173 |
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287 |
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Author |
Röttcher, K. |
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Book Chapter |
Year |
2018 |
Publication |
Risikomanagement und Nachhaltigkeit in der Wasserwirtschaft: Erfolgreiche Navigation durch die Komplexität und Dynamik des Risikos |
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165-174 |
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Im vorliegenden Beitrag werden beispielhaft unterschiedliche Ansätze des Risikomanagements und das Verständnis von Nachhaltigkeit in der Wasserwirtschaft dargelegt. Die Darstellung richtet sich insbesondere an Leser aus anderen Fachdisziplinen, wie das Rechts- und Finanzwesen, den Fahrzeug- und Maschinenbau oder auch die sozialen Berufe. Die Zusammenhänge werden überblicksartig mit einzelnen konkreten Beispielen dargestellt mit dem Fokus auf die grundsätzlichen Denk- und Vorgehensweisen. |
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Springer Fachmedien Wiesbaden |
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Wiesbaden |
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Michalke, A.; Rambke, M.; Zeranski, S. |
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978-3-658-19684-4 |
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THL @ christoph.kuells @ Röttcher2018 |
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90 |
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Rossetto, R.; Filippis, G.D.; Borsi, I.; Foglia, L.; Cannata, M.; Criollo, R.; Vázquez-Suñé, E. |
Title |
Integrating free and open source tools and distributed modelling codes in GIS environment for data-based groundwater management |
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Journal Article |
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2018 |
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Environmental Modelling & Software |
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107 |
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210-230 |
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Free and Open Source Software, FREEWAT, Groundwater management, ICT, MODFLOW, QGIS |
Abstract |
Integrating advanced simulation techniques and data analysis tools in a freeware Geographic Information System (GIS) provides a valuable contribution to the management of conjunctive use of groundwater (the world’s largest freshwater resource) and surface-water. To this aim, we describe here the FREEWAT (FREE and open source software tools for WATer resource management) platform. FREEWAT is a free and open source, QGIS-integrated interface for planning and management of water resources, with specific attention to groundwater. The FREEWAT platform couples the power of GIS geo-processing and post-processing tools in spatial data analysis with that of process-based simulation models. The FREEWAT environment allows storage of large spatial datasets, data management and visualization, and running of several distributed modelling codes (mainly belonging to the MODFLOW family). It simulates hydrologic and transport processes, and provides a database framework and visualization capabilities for hydrochemical analysis. Examples of real case study applications are provided. |
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1364-8152 |
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THL @ christoph.kuells @ rossetto_integrating_2018 |
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92 |
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Nijsten, G.-J.; Christelis, G.; Villholth, K.G.; Braune, E.; Gaye, C.B. |
Title |
Transboundary aquifers of Africa: Review of the current state of knowledge and progress towards sustainable development and management |
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Journal Article |
Year |
2018 |
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Journal of Hydrology: Regional Studies |
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20 |
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Pages |
21-34 |
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Africa, Assessment, Governance, Indicators, Transboundary aquifers |
Abstract |
Study region Transboundary aquifers (TBAs) of Africa. Study focus Review of work on TBAs in Africa, including an overview of assessments and management efforts that have taken place over the last half century. New hydrological insights Seventy-two TBAs have been mapped in Africa. They underlie 40% of the continent, where 33% of the population lives, often in arid or semi-arid regions. TBA inventories have progressed since 2000 and remain work in progress. Despite their importance only eleven TBAs have been subjected to more detailed studies. Cooperation has been formalised for seven TBAs. Most of these TBAs are in North Africa and the Sahel. The recent global Transboundary Waters Assessment Programme compiled information at the national level to describe TBAs in terms of key indicators related to the water resource, socio-economic, and legal and institutional conditions. Availability of data at national level is low, hampering regional assessment. Comparing indicators, from questionnaire surveys, with those from a global water-use model showed variable levels of agreement, calling for further research. Reports on agreements scoping TBA management, indicate that this may be dealt with within international river/lake agreements, but reported inconsistencies between TBA sharing countries also indicate that implementation is limited. Increasing awareness and support to joint TBA management is noticeable amongst international organisations. However, such cooperation requires long-term commitment to produce impacts at the local level. |
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2214-5818 |
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THL @ christoph.kuells @ nijsten_transboundary_2018 |
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93 |
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Author |
Burchi, S. |
Title |
Legal frameworks for the governance of international transboundary aquifers: Pre- and post-ISARM experience |
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Journal Article |
Year |
2018 |
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Journal of Hydrology: Regional Studies |
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20 |
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15-20 |
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International aquifers, International aquifers agreements, International groundwater law, UN draft articles on the law of transboundary aquifers |
Abstract |
Study region Africa, Latin America, Europe. Study focus Through the extensive study and mapping of the world’s aquifers that lie astride the international boundary lines of sovereign States, ISARM has awakened concerned States to the existence of aquifers stretching beyond their borders, and precipitated cooperation in generating a body of knowledge that facilitated cooperation in governance arrangements for such aquifers. In parallel, ISARM influenced the shape and direction of the United Nations “Draft articles on the law of transboundary aquifers” appended to UN Resolution 63/124 of 2008. Both stimulated cooperation among concerned States, and provided a frame of reference for the legal grounding of such cooperation in aquifer-specific agreements. New hydrological insights Through this synergistic paradigm, ISARM has made an impact on the shape and direction of cooperation in the Guaraní Aquifer in South America, and in the Iullemeden and Taoudeni/Tanezrouft Aquifer Systems (ITAS) in the Sahel region of Africa. It is having an influence on the shape and direction of cooperation being negotiated on the Stampriet Aquifer System in Southern Africa, and on the Ocotepeque-Citalá Aquifer in Central America. The link of ISARM to other international aquifer agreements on record is tenuous, and ISARM’s influence on their generation speculative. The visibility of ISARM has faded since 2012, however its legacy is lasting. |
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2214-5818 |
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THL @ christoph.kuells @ burchi_legal_2018 |
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100 |
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Priestley, S.C.; Payne, T.E.; Harrison, J.J.; Post, V.E.A.; Shand, P.; Love, A.J.; Wohling, D.L. |
Title |
Use of U-isotopes in exploring groundwater flow and inter-aquifer leakage in the south-western margin of the Great Artesian Basin and Arckaringa Basin, central Australia |
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Journal Article |
Year |
2018 |
Publication |
Applied Geochemistry |
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98 |
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Pages |
331-344 |
Keywords |
Activity ratios, Central Australia, Great Artesian Basin, Hydrogeology, Sequential extraction, Uranium isotopes |
Abstract |
The distribution of uranium isotopes (238U and 234U) in groundwaters of the south-western margin of the Great Artesian Basin (GAB), Australia, and underlying Arckaringa Basin were examined using groundwater samples and a sequential extraction of aquifer sediments. Rock weathering, the geochemical environment and α-recoil of daughter products control the 238U and 234U isotope distributions giving rise to large spatial variations. Generally, the shallowest aquifer (J aquifer) contains groundwater with higher 238U activity concentrations and 234U/238U activity ratios close to secular equilibrium. However, the source input of uranium is spatially variable as intermittent recharge from ephemeral rivers passes through rocks that have already undergone extensive weathering and contain low 238U activity concentrations. Other locations in the J aquifer that receive little or no recharge contain higher 238U activity concentrations because uranium from localised uranium-rich rocks have been leached into solution and the geochemical environment allows the uranium to be kept in solution. The geochemical conditions of the deeper aquifers generally result in lower 238U activity concentrations in the groundwater accompanied by higher 234U/238U activity ratios. The sequential extraction of aquifer sediments showed that α-recoil of 234U from the solid mineral phases into the groundwater, rather than dissolution of, or exchange with the groundwater accessible minerals in the aquifer, caused enrichment of groundwater 234U/238U activity ratios in the Boorthanna Formation. Decay of 238U in uranium-rich coatings on J aquifer sediments caused resistant phase 234U/238U activity ratio enrichment. The groundwater 234U/238U activity ratio is dependent on groundwater residence time or flow rate, depending on the flow path trajectory. Thus, uranium isotope variations confirmed earlier groundwater flow interpretations based on other tracers; however, spatial heterogeneity, and the lack of clear regional correlations, made it difficult to identify recharge and inter-aquifer leakage. |
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0883-2927 |
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THL @ christoph.kuells @ priestley_use_2018 |
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115 |
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