Carbonate minerals

AccessScience ◽  
2015 ◽  
Keyword(s):  
Energies ◽  
2021 ◽  
Vol 14 (12) ◽  
pp. 3662
Author(s):  
Hongzhi Yang ◽  
Liangbiao Lin ◽  
Liqing Chen ◽  
Yu Yu ◽  
Du Li ◽  
...  

The Longtan Formation of the Upper Permian in the Sichuan Basin has become a significant target for shale gas exploration in recent years. Multiple methods, including outcrop observations, thin sections, total organic matter content, X-ray diffraction and scanning electron microscopy were used to investigate the mineralogy, shale lithofacies assemblages and their relationships with the deposition environment. The mineral composition of the Longtan Formation has strong mineral heterogeneity. The TOC values of the Longtan Formation have a wide distribution range from 0.07% to 74.67% with an average value of 5.73%. Four types of shale lithofacies assemblages of the Longtan Formation could be distinguished, as clayey mudstone (CLS), carbonaceous shale (CAS), siliceous shale (SS) and mixed shale (MS) on the basis of mineral compositions. The TOC values of various types of shale lithofacies assemblages in the Longtan Formation varied widely. The shore swamp of the Longtan Formation is most influenced by the terrestrial input and mainly develops CLS and MS. The tidal flat is influenced by the terrestrial input and can also deposit carbonate minerals, developing CLS, CAS and MS. The shallow water melanged accumulation shelf develops CAS and MS, dominated by clay and carbonate minerals. The deep water miscible shelf develops CLS and SS, whose mineral composition is similar to that of the shore swamp, but the quartz minerals are mainly formed by chemical and biological reactions, which are related to the Permian global chert event. The depositional environment of the Longtan Formation controls the shale mineral assemblage of the Longtan Formation and also influences the TOC content.


Agronomy ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 512
Author(s):  
Michiele Gebrehiwet ◽  
Nata T. Tafesse ◽  
Solomon Habtu ◽  
Berhanu F. Alemaw ◽  
Kebabonye Laletsang ◽  
...  

This study evaluates the cause of salinization in an irrigation scheme of 100 ha supplied from a reservoir. The scheme is located in Gumselasa catchment (28 km2), Tigray region, northern Ethiopia. The catchment is underlain by limestone–shale–marl intercalations with dolerite intrusion and some recent sediments. Water balance computation, hydrochemical analyses and irrigation water quality analyses methods were used in this investigation. Surface waters (river and reservoir) and groundwater samples were collected and analyzed. The water table in the irrigated land is ranging 0.2–2 m below the ground level. The majority of groundwater in the effective watershed area and the river and dam waters are fresh and alkaline whereas in the command area the groundwater is dominantly brackish and alkaline. The main hydrochemical facies in the groundwater in the effective watershed area are Ca-Na-SO4-HCO3, Ca-Na- HCO3-SO4, and Ca-Na-Mg-SO4-HCO3. The river and dam waters are Mg-Na-HCO3-SO4 and HCO3-SO4-Cl types, respectively. In the command area the main hydrochemical facies in the groundwater are Ca-Na-HCO3-SO4 and Ca-Na-Mg-SO4-HCO3. Irrigation water quality analyses revealed that salinity and toxicity hazards increase from the effective watershed to the irrigated land following the direction of the water flow. The results also showed that the analyzed waters for irrigation purpose had no sodicity hazard. The major composition controlling mechanisms in the groundwater chemistry was identified as the dissolution of carbonate minerals, silicate weathering, and cation exchange. One of the impacts of the construction of the dam in the hydrologic environment of the catchment is on its groundwater potential. The dam is indirectly recharging the aquifers and enhances the groundwater potential of the area. This increment of availability of groundwater enhanced dissolution of carbonate minerals (calcite, dolomite, and gypsum), silicate weathering and cation exchange processes, which are the main causes of salinity in the irrigated land. The rising of the brackish groundwater combined with insufficient leaching contributed to secondary salinization development in the irrigated land. Installation of surface and subsurface drainage systems and planting salt tolerant (salt loving) plants are recommended to minimize the risk of salinization and salt accumulation in the soils of the irrigated land.


2020 ◽  
Vol 7 (21) ◽  
pp. 4197-4221 ◽  
Author(s):  
Francisco Colmenero ◽  
Jakub Plášil ◽  
Jiří Sejkora

The structure, hydrogen bonding, X-ray diffraction pattern and mechanical properties of six important uranyl carbonate minerals, roubaultite, fontanite, sharpite, widenmannite, grimselite and čejkaite, are determined using first principles methods.


Icarus ◽  
2008 ◽  
Vol 195 (1) ◽  
pp. 493-503 ◽  
Author(s):  
Frans J.M. Rietmeijer ◽  
Aurora Pun ◽  
Yuki Kimura ◽  
Joseph A. Nuth

We present an overview of geochemical data from pore waters and solid phases that clarify earliest diagenetic processes affecting modern, shallow marine carbonate sediments. Acids produced by organic matter decomposition react rapidly with metastable carbonate minerals in pore waters to produce extensive syndepositional dissolution and recrystallization. Stoichiometric relations among pore water solutes suggest that dissolution is related to oxidation of H 2 S which can accumulate in these low-Fe sediments. Sulphide oxidation likely occurs by enhanced diffusion of O 2 mediated by sulphide-oxidizing bacteria which colonize oxic/anoxic interfaces invaginating these intensely bioturbated sediments. Buffering of pore water stable isotopic compositions towards values of bulk sediment and rapid 45 Ca exchange rates during sediment incubations demonstrate that carbonate recrystallization is a significant process. Comparison of average biogenic carbonate production rates with estimated rates of dissolution and recrystallization suggests that over half the gross production is dissolved and/or recrystallized. Thus isotopic and elemental composition of carbonate minerals can experience significant alteration during earliest burial driven by chemical exchange among carbonate minerals and decomposing organic matter. Temporal shifts in palaeo-ocean carbon isotope composition inferred from bulk-rocks may be seriously compromised by facies-dependent differences in dissolution and recrystallization rates.


Radiocarbon ◽  
1992 ◽  
Vol 34 (3) ◽  
pp. 646-653 ◽  
Author(s):  
Songlin Cheng

Since the pioneer publication of K. O. Münnich (1957), 14C systematics have been used in many hydrogeological studies. Because of the complexity of carbon geochemistry, numerous models have been proposed to correct the dilution effect of “dead” carbon in groundwater. All the 14C correction models for dating groundwater are based on either open- or closed-system conditions. I present here a simple model that accounts for the effects of both open- and closed-system dissolution of carbonate and aluminosilicate minerals. For systems involving precipitation of carbonate minerals and redox reactions of organic matter, reaction-path simulations are essential for reliable 14C dating of groundwater.


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