Sodium-bicarbonate groundwaters in southeastern West Siberia, Russia: Compositions, types, and formation conditions; Applied Geochemistry; Vol. 116

Dades bibliogràfiques
Parent link:Applied Geochemistry
Vol. 116.— 2020.— [104579, 11 p.]
Autor principal: Lepokurova О. Е. Olesya Evgenyevna
Autor corporatiu: Национальный исследовательский Томский политехнический университет Инженерная школа природных ресурсов Отделение геологии
Sumari:Title screen
Sodium-bicarbonate HCO3–Na (sodic) groundwaters exist throughout southeastern West Siberia at approximate depths from 50–300 m to 1.0–2.3 km in Mesozoic-Cenozoic sediments. They belong to five main types of fresh (I), brackish (II), high-pH low-saline (III), coal-related saline (IV), and carbonated (V) waters that differ in composition, as well as in depth and lateral extent. Waters of types I and II are of regional extent and common chemistry, while those of three other types have specific compositions and are restricted to local areas. Isotope data (d18O, dD, d13C) indicate that waters of all five types originated by the infiltration mechanism; type IV water has an enriched oxygen isotope composition; all water types except V have biogenic carbon sources. As shown by thermodynamic calculations, all HCO3–Na waters are nonequilibrium with many primary aluminosilicate minerals bur are equilibrated with carbonates and clay minerals. The number of minerals equilibrated with these waters increases progressively from type I to IV with salinity and pH. The obtained data allow reconstructing the formation of sodic waters of different types in the context of the evolution in the system ‘water – rock – gas – organic matter’. The formation scenario is the same for all types of water: dissolution of sedimentary aluminosilicate minerals which are not in equilibrium with the waters and concurrent precipitation of carbonates. Waters in the zone of slow water exchange at depths from 100 to 300 m acquire the HCO3–Na compositions, with TDS >0.7–0.8 g/L and ?H >7.6. The diversity of the waters results from difference in their residence time, even during the formation of HCO3–Na chemistry (types I and II), and from environment effects: presence of inorganic CO2 (V) and organic carbon (IV) sources or their absence (III).
Режим доступа: по договору с организацией-держателем ресурса
Idioma:anglès
Publicat: 2020
Matèries:
Accés en línia:https://doi.org/10.1016/j.apgeochem.2020.104579
Format: Electrònic Capítol de llibre
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=662809

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200 1 |a Sodium-bicarbonate groundwaters in southeastern West Siberia, Russia: Compositions, types, and formation conditions  |f О. Е. Lepokurova 
203 |a Text  |c electronic 
300 |a Title screen 
330 |a Sodium-bicarbonate HCO3–Na (sodic) groundwaters exist throughout southeastern West Siberia at approximate depths from 50–300 m to 1.0–2.3 km in Mesozoic-Cenozoic sediments. They belong to five main types of fresh (I), brackish (II), high-pH low-saline (III), coal-related saline (IV), and carbonated (V) waters that differ in composition, as well as in depth and lateral extent. Waters of types I and II are of regional extent and common chemistry, while those of three other types have specific compositions and are restricted to local areas. Isotope data (d18O, dD, d13C) indicate that waters of all five types originated by the infiltration mechanism; type IV water has an enriched oxygen isotope composition; all water types except V have biogenic carbon sources. As shown by thermodynamic calculations, all HCO3–Na waters are nonequilibrium with many primary aluminosilicate minerals bur are equilibrated with carbonates and clay minerals. The number of minerals equilibrated with these waters increases progressively from type I to IV with salinity and pH. The obtained data allow reconstructing the formation of sodic waters of different types in the context of the evolution in the system ‘water – rock – gas – organic matter’. The formation scenario is the same for all types of water: dissolution of sedimentary aluminosilicate minerals which are not in equilibrium with the waters and concurrent precipitation of carbonates. Waters in the zone of slow water exchange at depths from 100 to 300 m acquire the HCO3–Na compositions, with TDS >0.7–0.8 g/L and ?H >7.6. The diversity of the waters results from difference in their residence time, even during the formation of HCO3–Na chemistry (types I and II), and from environment effects: presence of inorganic CO2 (V) and organic carbon (IV) sources or their absence (III). 
333 |a Режим доступа: по договору с организацией-держателем ресурса 
461 |t Applied Geochemistry 
463 |t Vol. 116  |v [104579, 11 p.]  |d 2020 
610 1 |a электронный ресурс 
610 1 |a труды учёных ТПУ 
610 1 |a HCO3-Na groundwater 
610 1 |a water chemistry 
610 1 |a system 'water-aluminosilicate rock-gas-organic matter' 
610 1 |a equilibrium 
610 1 |a formation mechanism and conditions 
610 1 |a West Siberia 
610 1 |a подземные воды 
610 1 |a равновесие 
610 1 |a условия образования 
610 1 |a Западная Сибирь 
700 1 |a Lepokurova  |b О. Е.  |c geologist  |c Professor of Tomsk Polytechnic University, Doctor of Geological and Mineralogical Sciences  |f 1980-  |g Olesya Evgenyevna  |3 (RuTPU)RU\TPU\pers\32568  |9 16489 
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