Dissolution Of Silicate Minerals Research Articles

Dissolution process and mechanism of montmorillonite in oxalic acid and sulfuric acid media at various pH levels

The dissolution of silicate minerals plays a crucial role in many natural geological processes. In order to better comprehend the reaction mechanisms and dissolution characteristics of montmorillonite in different acidic systems, the effects of interfacial reactions of montmorillonite with oxalic and sulfuric acid solutions at various pH levels on the ionic dissolution, crystal structure, and micro-morphology were studied, and the morphology of aluminum and saturation index of secondary mineral were simulated. It was shown that the dissolution amounts of Mg2+, Al3+ and Si4+ in montmorillonite structure decreased with the increase of pH value, which reflected the dependence of montmorillonite dissolution on the pH value of solution. The dissolution percentages of Mg2+, Al3+ and Si4+ after the reaction of montmorillonite with oxalic acid solution were greater than those in sulfuric acid solution, and the highest dissolution rate of Al3+, indicated that both ligands and protons attacked the surface sites of montmorillonite and accelerated the dissolution of ions. Moreover, oxalate ligands exerted specific binding effects on Al3+ ions. While reacting with oxalate and sulfate, the tetrahedral, octahedral and interlayer cations of montmorillonite exhibited the non-stoichiometric and inconsistent dissolution. The oxalate ligands have a strong complexation effect on Al3+, so that Al3+ in oxalate solution exists in the form of aluminum oxalate complex, which reduces the effective concentration of Al3+ in solution and promotes the dissolution of Al3+ in montmorillonite structure. The Mg2+ ions settled at octahedral substitution sites possessed weak stability, while those from the interlayer featured strong interlayer interchangeability, demonstrating the dissolution percentage up to 10.85 % and 8.62 % even in oxalic and sulfuric acid solutions at pH of 6.5. All secondary mineral phases in the solution were undersaturated, making the montmorillonite dissolution difficult to balance. Montmorillonite has a high cation exchange capacity, which makes it have a strong buffer capacity to exogenous acids. This study helps to explain the dissolution process of montmorillonite in inorganic and organic acid solutions at different pH value.

Distribution and genesis of geothermal waters in the Xianshuihe fault zone, Western Sichuan plateau, China: Constraints on fracture system and regional seismic activities

The Xianshuihe fault zone (XSFZ), which is characterized by intense tectonic activities, frequent earthquakes and great number of hot springs, has significant potential for exploiting geothermal resources. Previous studies primarily focus on certain hydrothermal systems in southeastern segment of XSFZ, such as Kangding hydrothermal system, but lack the synthetical comparison and systematic analysis of geothermal waters along the XSFZ. Based on detailed geological investigation, the XSFZ hydrothermal system has divided into six geothermal activity areas: Luhuo (LH), Daofu (DF), Qianning-Bamei (QB), Yalahe-Zhonggu (YZ), Kangding (KD) and Moxi (MX). According to the 87Sr/86Sr ratios and elements behaving in water-rock interactions, the dissolution of silicate minerals is the primarily source of the hydrogeochemical compositions in geothermal waters. The δD and δ18O composition indicate that geothermal waters primarily originated from meteoric waters, but also affected by deep fluids. However, the contribution of deep fluids to the southeastern geothermal areas (YZ, KD and MX) with high concentrations of Cl- is greater than that of the northwestern (LH, DF and QB). The reservoir temperatures and chlorine-enthalpy model reveal that there are three distinct geothermal systems along the XSFZ: YZ and KD geothermal waters are originated from a common deep reservoir (R1), MX are from R3, and LH, DF, and QB are from R4. Due to the uneven thermal structural distribution along XSFZ, the southeastern segments generated stronger thermal stress and have more frequent earthquake occurrence. Thus, the study of geothermal waters along XSFZ can provide valuable insights into deep tectonic activities and geochemical indicators of earthquake monitoring in the region.

Hydrogeochemical and isotopic investigations of groundwater in the reclaimed desert located between EL Nasr canal and Mariut Tableland, NW Coast, Egypt

A complete understanding of groundwater dynamics and its interaction with surface water under the impact of agricultural activities is vital for local agriculture, ecology, and residents of dry regions, which is not commonly recognized in arid areas. This research outlines the geochemical characteristics, recharge sources, and potential factors impacting groundwater quality in a new land reclamation located in the small basin of Abu Mina, which is part of the Western Nile Delta region.1 Thirty-one groundwater samples and two surface water samples were collected in 2021 to represent the Pleistocene aquifer and were subjected to multivariate statistical, hydrochemical, and stable isotope analyses. Data analysis demonstrates that Na+ > Ca2+ > Mg2+ > K+ and SO42– > Cl– > HCO3– > NO3– are the predominant cations and anions, respectively. Groundwater salinity ranged from 465.60 to 6455.18 mg/l, with slightly alkaline. Most of the water samples fall into one of three types of facies: Ca–Cl, Na–Cl, and Mixed Ca–Mg–Cl, in decreasing order. The meteoric genesis index (r2) indicates that deep meteoric water percolation dominates the Pleistocene aquifer. The aquiline diagrams, correlation matrix, and different ionic ratios indicate that evaporation, reverse ion exchange reactions, and the dissolution of carbonate and silicate minerals are the main processes governing groundwater chemistry. Factor analysis (FA) indicated that three factors explain groundwater hydrochemistry, accounting for 71.98% of the total variance. According to the rotating components matrix (F1–F3), the chemistry of the Quaternary aquifer is principally affected by evaporation, ion exchange reactions, and anthropogenic influences. Additionally, salinity increases due to the return flow of irrigation activities and mixing between old and recent water. The stable isotopes (δ18O and δ2H) indicate that the Quaternary aquifer receives groundwater recharge through the return flow of excess irrigation and canal seepage. Under desert reclamation conditions, groundwater salinization processes should be given special consideration. All groundwater samples are appropriate for agricultural irrigation based on the Sodium Adsorption Ratio (SAR), Permeability Index (PI), Percent Sodium (%Na), and Residual Sodium Carbonate (RSC).

Comprehending Spatial Distribution and Controlling Mechanisms of Groundwater in Topical Coastal Aquifers of Southern China Based on Hydrochemical Evaluations

Groundwater quality and availability in coastal aquifers have become a serious concern in recent times due to increased abstraction for domestic, agricultural and industrial purposes. (1) Background: Zhuhai city is selected as a representative coastal aquifer in Southern China to comprehensively evaluate the hydrochemical characteristics, spatial distribution and controlling mechanisms of groundwater. (2) Methods: A detailed study utilizing statistical analyses, a Piper diagram, Gibbs plots, and ion ratios was conducted on 114 surface water samples and 211 groundwater samples. (3) Results: The findings indicate that the pH of most groundwater is from 6.06 to 6.52, indicating a weakly acidic environment. The pH of surface water ranges from 5.35 to 9.86, with most values being weakly alkaline. The acidity in the groundwater may be related to the acidic atmospheric precipitation, an acidic unsaturated zone, oxidation of sulphide minerals and tidal action. The groundwater chemical types are predominantly mixed, followed by Ca-Mg-HCO3 type. Surface water samples are predominantly Na-Cl-SO4 type. The NO3− concentration in groundwater is relatively high, with a mean value of 17.46 mg/L. The NO2− and NH4+ concentrations in groundwater are relatively low, with mean values of 0.46 mg/L and 7.58 mg/L. (4) Conclusions: The spatial distribution of the principal chemical constituents in the groundwater is related to the landform. The chemical characteristics of groundwater in the study area are mainly controlled by the weathering and dissolution of silicate and sulfate minerals, evaporation, seawater mixing and cation exchange. Nitrate in clastic fissure groundwater, granite fissure groundwater and unconfined pore groundwater primarily originates from atmospheric precipitation, agricultural activities of slope farmland and forest land. Nitrate in confined pore groundwater and karst groundwater primarily originates from domestic sewage and mariculture wastewater. Our findings elucidate the processes characterizing the hydrogeology and surface water interactions in Zhuhai City’s coastal system, which are relevant to other catchments with similar geological characteristics.

Chemical and isotopic constraints on fluid origin and genesis of geothermal systems in the Tingri-Tangra Yumco rift, southern Tibetan Plateau

Numerous geothermal systems are hosted by extensional rifts that transect the Himalayas and Lhasa block in the Himalayan–Tibetan orogen. However, the relationships between hydrogeological processes and geothermal fluid circulation in different tectonic units remain unclear. Here, we report an integrated dataset of chemical and isotopic compositions (including major and trace elements, δD, δ18O, and 87Sr/86Sr) of thermal spring water from the Tingri-Tangra Yumco rift to assess their origins and circulation processes. δ18O (− 21.3 to − 17.0‰) and δD (− 166 to − 135‰) values of thermal springs indicate dominant recharge of meteoric waters from areas with elevation of > 6000 m and minor addition of magmatic fluids. Meteoric water could infiltrate to depths of about 1700–2900 m along the faults, whereby it is influenced by geothermal gradient and/or conductive heat transfer of magmatic fluids. The thermal spring waters are mainly Na-HCO3 type and are controlled by dissolution of silicate and carbonate minerals and mixing with deep fluids. The results of chemical and multicomponent geothermometers indicate reservoir temperatures of 115 − 195 ℃, corresponding to a convection heat flux of 3.96 × 105 J/s to 1.78 × 107 J/s from geothermal systems, which are comparable to that of the low-enthalpy geothermal systems in southern Italy. Geochemical modeling is conducted to assess the water–mineral equilibria in the reservoir. Trace elements and 87Sr/86Sr data suggest spatially variable controlling factors for the rift-related geothermal systems: (1) interaction with granitoid and carbonate in the Himalayas; (2) cold groundwater mixing with that leaching from granite and volcanic rocks in the Lhasa block; (3) the input of vapors from magmatic degassing. The geochemistry of thermal springs associated with extensional rift is largely induced by the interaction between fluid and different reservoir rocks in the Himalayas and Lhasa block. Based on these findings, a genetic model is proposed for exploration and development of geothermal resources in the Tingri-Tangra Yumco rift.

Hydrochemical and Formation Mechanism Studies of Groundwater in Quaternary Aquifer in a Northern Plain of China: An Example of Beijing Plain

Beijing Plain is a very active part of Beijing city regarding the socio-economic and human activities of the region. Over the past four decades, Beijing’s economic development and the continuous drought for nearly 10 years in the 2000s have negatively impacted the groundwater quantity and quality. Therefore, it is necessary to investigate the present situation of groundwater chemistry in this region to develop a comprehensive database and orientation for future research on groundwater quality evaluation. Mathematical statistics, Piper’s trilinear diagram, Gibbs plots, the ion ratio method and PHREEQC software 3.7.3 were used to analyze the groundwater hydrogeochemical characteristics and formation mechanisms of the quaternary aquifers of the Beijing Plain area. Hydrogeochemical results indicated that the groundwater is slightly alkaline, with pH values ranging from 6.76 to 8.65 and an average value of 7.92. The order of major cations in groundwater was Ca2+ > Na+ > Mg2+ > K+ with average values of 66.54 mg/L, 50.58 mg/L, 23.78 mg/L, and 1.81 mg/L, respectively, while the order of major anions was HCO3− > SO42− > Cl− with average values of 284.89 mg/L, 52.1 mg/L and 35.5 mg/L, respectively. The groundwater chemical types are Mg-Ca-Cl-HCO3, Na-Ca-HCO3, Mg-Ca-HCO3 and Mg-Na-HCO3. Research on the main influencing factors and PHREEQC hydrogeochemical inverse simulations results along the four pathways selected confirmed that rock weathering with sulfate, silicate and carbonate rock mineral dissolution and Na+, Mg2+ and Ca2+ ion reaction exchange influenced groundwater hydrogeochemical characteristics of the quaternary aquifers of the Beijing Plain area. Understanding the formation mechanisms of hydrogeochemistry in quaternary plains provides guidance for future studies and, through suggestions and case studies, facilitates decision-making by policy-makers on the sustainable management of groundwater resources.

The impact of adsorption–desorption reactions on the chemistry of Himalayan rivers and the quantification of silicate weathering rates

Common environmental adsorbents (clay minerals, metal-oxides, metal-oxyhydroxides and organic matter) can significantly impact the chemistry of aqueous fluids via adsorption–desorption reactions. The dissolved chemistry of rivers have routinely been used to quantify silicate mineral dissolution rates, which is a key process for removing carbon dioxide (▪) from the atmosphere over geological timescales. The sensitivity of silicate weathering rates to climate is disproportionately weighted towards regions with high erosion rates. This study quantifies the impact of adsorption-desorption reactions on the chemistry of three large Himalayan rivers over a period of two years, utilising both the adsorbed and dissolved phases. The concentration of riverine adsorbed cations are found to vary principally as a function of the concentration and cation exchange capacity (CEC) of the suspended sediment. Over the study period, the adsorbed phase is responsible for transporting ∼70% of the mobile (adsorbed and dissolved) barium and ∼10% of the mobile calcium and strontium. The relative partitioning of cations between the adsorbed and dissolved phases follows a systematic order in both the monsoon and the dry-season (preferentially adsorbed: Ba > Sr & Ca > Mg & K > Na). Excess mobile sodium (▪=Na-Cl) to silicon (Si) riverine ratios are found to vary systematically during an annual hydrological cycle due to the mixing of low temperature and geothermal waters. The desorption of sodium from uplifted marine sediments is one key process that may increase the Na*/Si ratios. Accounting for the desorption of sodium reduces silicate weathering rate estimates by up to 83% in the catchments. This study highlights that surficial weathering processes alone are unable to explain the chemistry of the rivers studied due to the influence of hydrothermal reactions, which may play an important role in limiting the efficiency of silicate weathering and hence modulating atmospheric ▪ concentrations over geological time.

Characteristics of congruent dissolution of silicate minerals enhanced by chelating ligand under ambient conditions

Abstract Natural and anthropogenic chelating ligands play important roles in promoting mineral dissolution during water-rock interactions. To address the remaining issue of how chelating ligands participate in the dissolution of minerals, this study investigated the dissolution characteristics of seven types of silicate minerals in the presence of a chelating ligand, N,N-bis(carboxymethyl)-L-glutamic acid (GLDA), which is a glutamic acid derivative, through batch dissolution experiments. The results showed that the dissolution of all types of silicate minerals, i.e., olivine (nesosilicate), epidote (sorosilicate), tourmaline (cyclosilicate), enstatite (single-chain inosilicate), hornblende (double-chain inosilicate), biotite (phyllosilicate), and anorthite (tectosilicate), can be enhanced by up to two orders of magnitude at both pH 4 and 8. The chelating ligand particularly facilitated the dissolution of minerals with a higher Al content, such as tourmaline and anorthite. Furthermore, the presence of chelating ligands enhanced the leaching of not only metals but also Si from minerals, resulting in a more congruent characteristic of mineral dissolution. A possible mechanism is that the chelating ligand adsorbs onto the negatively charged the mineral surface, which attracts more H+ and polarizes Si-O and Mg-O bonds, thereby dissolving the minerals at a faster rate. These results have significant implications for understanding the dissolution of minerals in nature and for the application of chelating agents in geological and materials engineering.

Geochemical characteristics, mechanisms, and suitability of groundwater resource for sustainable water supply in Quetta valley

ABSTRACT Groundwater is a crucial water resource for various usages worldwide. The Quetta Valley of Pakistan was investigated regarding its groundwater quality sustainability based on integrated approaches of hydrochemistry, geographic information system, and multivariate statistics. A total of 29 groundwater samples were collected from monitoring wells to get insights into the hydrochemical suitability of groundwater for sustainable irrigation and drinking utilization. The results indicate groundwater is mainly featured by the hydrochemical facies of HCO3·Cl-Ca. Groundwater hydrochemical composition is dominantly governed by the dissolution of carbonates and silicate minerals in combination with positive cation exchange in the valley. Principal component analysis reveals a significant influence of geogenic factors on groundwater chemistry, further supported by PHREEQC simulation that detects a supersaturation of calcite, dolomite, and sulphate minerals in the aquifer. The irrigation water quality index divides groundwater in the study area into three zones, which signify low restriction and no restriction, except for a severe restriction in the southwestern part of the valley. Groundwater is generally suitable for irrigation across the valley. The entropy-weighted water quality index classifies groundwater as excellent and good quality for drinking. This study can provide crucial insights for authorities on groundwater suitability in Quetta Valley and similar regions worldwide.

Geochemistry and sources of boron and strontium of geothermal waters from the Pearl River Delta region, South China: Implications for water-rock interactions

Pearl River Delta (PRD) region of South China is abundant of geothermal water resources. However, the development and utilization level of geothermal resources in this region is relatively low, due in part to the lack of fundamental geochemical research. To access water-rock interaction processes of the PRD geothermal system, we analyzed the geochemistry of geothermal waters by combining trace elements (B, Sr, and Br) and isotopes (δ11B and 87Sr/86Sr) with conventional tracers (major elements) that had been reported. The Cl/Br ratios (from 31 to 639) confirm the multi-source salinity of marine origin, precipitation, and a minor dissolution of halite. Major ions chemistry highlights the influence of ions exchange, the dissolution of carbonate, silicate, and sulphate minerals as well as the contribution of seawater. The Cl/B ratios (61 to 22,583) suggest interactions with carbonate rock and felsic rock, input of seawater, and groundwater mixing. Boron isotopic compositions (δ11B) range between −9.22 and +39.78 ‰. Sr contents and 87Sr/86Sr ratios are more homogeneous, falling between 0.06 and 32.26 mg/L and between 0.71239 and 0.72121, respectively. The B and Sr isotopic signatures show that three processes contribute to geochemistry of geothermal waters: 1) water/rock interaction involving marine carbonate rock, evaporite, and granitoid or/and gneiss, 2) seawater intrusion, and 3) shallow groundwater mixing. Major-trace element chemistry and these isotope systematics on their own indicates essential information on the aspects of fluid origin or water-rock interaction processes, and however provide a more comprehensive understanding of the geothermal system in the PRD region, South China.

Genetic mechanism of geothermal water in the sandstone reservoir of western Sichuan, SW China: Evidence from hydrochemistry and δD − δ18O isotopes

Geothermal energy is the vital clean and renewable energy in the world. In China, most of high−temperature sedimentary − type geothermal waters are developed in western Sichuan, such as geothermal springs in the Litang county. In this study, hydrochemistry and δD − δ18O isotopes were investigated to clarify the genetic mechanism of high−temperature sedimentary − type geothermal waters in the Litang county. The self-organized map and Piper diagram showed three hydrochemical types of geothermal waters: (1) HCO3 − SO4 − Na, (2) HCO3 − Na with low Cl− concentration, (3) HCO3 − Na with high Cl− concentration. Cluster 1 geothermal water of Na − HCO3 − SO4 was dominated by dissolution of silicate and sulfate minerals. Cluster 2 geothermal water of HCO3 − Na with low Cl− concentration was affected by dissolution of silicate and CO2 degassing and mixed by large amounts of shallow cold water. Cluster 3 geothermal water of HCO3 − Na with high Cl− concentration was affected by dissolution of sandstone silicate and CO2 degassing and mixed by less shallow cold water. The recharge elevation of geothermal water in Litang ranges from 4799 to 4972 m, with an average of 4915 m. This suggests that the recharge sources of geothermal water are snow melt water and magmatic water. Cluster 3 geothermal water displayed the largest contribution of magmatic water. The temperature of HCO3 − SO4 − Na geothermal water after mixing is 92−102 °C, with an average of 97 °C; the initial temperature of HCO3 − Na with low Cl− geothermal water is 60−72 °C, with an average of 65 °C; the initial temperature of HCO3 − Na with high Cl− geothermal water is 74−91 °C, with an average of 81 °C. The temperature of geothermal water after mixing is Class 1 > Class 3 > Class 2. From the perspective of reservoir temperature, the Class 3 of geothermal water had the highest values, followed by Class 1 and Class 2 of geothermal water. From the perspective of cold − water mixing ratio, Class 2 and Class 3 of geothermal water had a similar mixing ratio, slightly higher than that of Class 1 of geothermal water. Therefore, the class 3 geothermal water with HCO3 − Na with high Cl− concentration possess the great potential for exploitation.

Constructing a map of potassium inputs to paddy fields from irrigation

Geographical and geological parameters, including land use, lithology, and water quality, and volume of irrigation were investigated to map K inputs into paddy fields from irrigation in the eastern part of Fukushima, Japan. This area has had one of the greatest needs for K maintenance worldwide due to the control of radiocesium uptake by plants after the Fukushima nuclear accident in 2011. The K+ concentration in irrigation water and its sources was in the range of 0.2–5.2 mg L−1, which was probably affected by both the natural conditions (e.g., amount of silicate mineral dissolution and presence of hot springs and coal seams) and human activities (e.g., agriculture and urbanization). Irrigation volume was estimated to range from 306 to 2300 mm in response to daily water requirement rates. K inputs were computed by multiplying the concentrations and volumes, giving estimated inputs of 2.5–133 kg K2O ha−1 crop−1. The inputs proved spatially variable and were high in the western and southeastern parts of the study area. Irrigation was estimated to supply more than half of the K application rate in the rice cultivation guidelines to 12% of the paddy field area. This map should provide useful information for devising K maintenance plans.

Hydrochemical Characteristics, Controlling Factors and Strontium Enrichment Sources of Groundwater in the Northwest Plain of Shandong Province, China

To elucidate the hydrochemical characteristics, controlling factors, sources and mechanisms of strontium ion enrichment in groundwater in the northwest plain of Shandong Province, China, 88 groundwater samples were collected, including 51 shallow pore groundwater samples, 29 deep pore groundwater samples and 8 karst groundwater samples. The hydrochemical characteristics of the different types of groundwater were quite different. The karst groundwater samples were all fresh water with a single hydrochemical type, either HCO3-Ca or HCO3-Ca·Mg. The deep pore groundwater samples were mainly brackish water, and the shallow pore groundwater samples were brackish water–salt water, which has complex hydrochemical types. The hydrochemical characteristics of all the types of groundwater were controlled by mineral dissolution and active positive cation exchange. In shallow pore groundwater, deep pore groundwater and karst groundwater, the dissolution of silicate, evaporite and carbonate minerals dominated the hydrogeochemical process. The strontium in groundwater was derived from the dissolution of minerals with strontium isomorphism. The average contents of strontium in shallow, deep and karst groundwater were 1.59 mg/L, 0.58 mg/L and 0.50 mg/L, respectively. The strontium in shallow pore groundwater was mainly derived from the enrichment of groundwater runoff, and its sources are abundant, with silicic rock being the main source. The deep pore groundwater mainly derived from the evaporative minerals containing strontium, and the karst water mainly derived from carbonate rock dissolution with similar characteristics.

Soil Inorganic Carbon Formation and the Sequestration of Secondary Carbonates in Global Carbon Pools: A Review

Soil inorganic carbon (SIC), a potential carbon sink especially in arid and semi-arid environments, contributes to soil development, landscape stability, carbon (C) sequestration, and global C dynamics but due to the lack of SIC scientific reporting in most C sequestration research, its importance is unclear. A detailed overview of primary and secondary carbonate occurrence, formation, and importance is much needed to understand the role of pedogenic (PC)/secondary carbonate (a common biogeochemically derived soil mineral over time) in the SIC. The mechanisms involved in the formation of PC including carbon dioxide (CO2) from microbial respiration and precipitation, silicate mineral weathering, dissolution, and reprecipitation are highlighted. The isotopic composition of carbonates related to biological C3 or C4 carbon fixation pathways and other paleoecologic and/or climactic factors responsible for new soil carbonate formation are discussed in detail. To address the lack of knowledge associated with SIC, this review attempts to highlight the currently known aspects of the literature, and briefly describe the formation and methodologies that can aid in addressing the research gaps surrounding SIC sequestration. The authors also suggest that greater focus needs to be provided on the actual measurement of SIC to develop a more comprehensive SIC inventory to provide sound data for future research direction, and modeling efforts and to predict C terrestrial storage and change efficiently.

A combination of multivariate statistics and machine learning techniques in groundwater characterization and quality forecasting

Globally, the quality of groundwater has proven to have been affected by some natural and human activities in recent years. To ensure there is good drinking water (Sustainable Development Goal 6.3, there is a need to elucidate the groundwater quality status of the area of interest. The groundwater in the northwestern parts of Ghana is not yet well characterized. Hence, this study employed a multi-method approach of hydrochemistry, water quality index (WQI), multivariate statistics, and machine models: multiple linear regression (MLR), decision tree regression (DTR), random forest regression (RFR), and artificial neural network (ANN), are combined in the characterization and prediction of the water quality in the area. They are robust in providing conclusions on groundwater assessment that can be relied upon for decision-making processes regarding groundwater usage and monitoring. Except for NO3− and TDS exceeding their standard levels in 22 and 2 locations, respectively, the other physicochemical parameters are within acceptable limits. The groundwater is generally good for domestic usage based on the WQI, with 79.2% of excellent to good waters. The groundwater evolved from Na-type, Cl-type, and Cl(SO4)-Ca(Mg) facies. Agricultural activities are the main source of human impact on the groundwater. Silicate mineral dissolution and ion exchange processes are the natural processes that affect groundwater mineralization, with mineral dissolution being the dominant process. Based on the performance metrics: MAE, MSE and RMSE of the ML methods considered in the WQI forecasting, the order of performance of the models is ANN > RFR > DTR > MLR, with the following respective R2 values 0.9974, 0.9193, 0.8966 and 0.8886.

Muddy sediments are an important potential source of silicon in coastal and continental margin zones

The dissolution of silicate minerals on the seafloor releases an important amount of dissolved silicon (dSi), which is necessary for maintaining high diatom production in Coastal and Continental Margin Zones (CCMZs). However, the dissolution of silicate minerals along the continental shelves is variable, which hinders our understanding of the marine Si cycle on both a regional and global scale. To understand the discrepancy of silicon (Si) released in different sediment matrices and its potential controlling factors, we investigated surface sediments of typical CCMZs of the Chinese marginal Seas using a continuous alkaline extraction technique, grain size and chemical (carbon and total nitrogen) analysis as well as a qualitative measurement of clay mineral composition by X-ray diffraction. The results showed that the amount of Si and aluminum (Al) leached from muddy sediments were 2 times greater than those released from sandy sediments. High dissolution rates (> 0.20 mg-SiO2 g−1 min−1) of silicate minerals are caused by a large sediment-specific surface area. Further, our data showed that biogenic silica (bSi) with high Al content (Si:Al < 40) has low reactivity and that the source of Al incorporated in bSi is silicate minerals undergoing dissolution. We show that although the dissolution of silicate minerals is less active than that of bSi, it still potentially releases more bio-available Si and Al to seawater due to its dominant presence on the seafloor (70.3% − 99.0%wt). This study highlights silicate minerals as an important potential marine Si source and emphasizes the need for a better understanding of the roles of silicate minerals in the Si cycle of marginal seas in future studies.

Hydrogeochemical and geothermal features of thermal springs along the Ganzi-Yushu fault, eastern Tibetan Plateau and its geological implications

Important fault zone processes can be discerned from the hydrothermal fluid circulation associated with active seismic sources. This study focused on the geochemical and isotopic features of the thermal waters along the Ganzi-Yushu fault (GZYSF) located in the eastern Tibetan Plateau. 22 spring samples were collected to characterize the chemical compositions and calculate the geothermal reservoir temperatures. The hydrothermal waters are mainly recharged by meteoric water based on the δ18O and δ2H values. Immature waters with a Na + -HCO3- or Ca2+(Mg2+)-HCO3- composition were recognized in the study area, combined with the poor correlation between K+, Na+, Mg2+, HCO3− and Cl− suggesting a shallow hydrothermal fluid source. The 87Sr/86Sr ratios and high concentrations of B (from 20.3 to 9445 μg/L) and Li (from 3.04 to 2380 μg/L) show a dissolution of silicate minerals containing calcium and magnesium during fluid circulation. The geothermometry in the silicon-enthalpy system suggested equilibrium temperatures up to 146 °C, whereas most are low temperatures. The shallow geothermal fields along GZYSF show that most large earthquakes (M＞5) were distributed in the transitional zone between high-value area and low-value area of the shallow geothermal field, suggesting a potential genetic link between geothermal field structure and earthquake nucleation along active faults. In conclusion, we proposed a conceptual model to portray the fluid circulation process. Such work can provide insights into the potential geothermal resource in Tibetan Plateau, and also investigate the processes controlling the fluid chemistry and the correlation with occurrence of earthquakes in the region.

Geochemical Evidence Constraining Genesis and Mineral Scaling of the Yangbajing Geothermal Field, Southwestern China

The Yangbajing geothermal field, a renowned high-temperature geothermal resource in Tibet of southwestern China, has been utilized for power generation for several decades. To improve geothermal exploitation in the Yangbajing, genesis and mineral scaling have yet to be further revealed. In this study, hydrochemistry and D-O-Sr isotopy were employed for analyzing genesis and mineral scaling in the Yangbajing geothermal field. The geothermal waters were weakly alkaline and had a high TDS content (1400–2900 mg/L) with the Cl-Na, Cl·HCO3-Na, and HCO3·Cl-Na types. The dissolution of silicate minerals (sodium and potassium feldspars) and positive cation exchange controlled the hydrogeochemical process. The geothermal water was recharged from snow-melted water and meteoric water originating from the Nyainqentanglh Mountains and Tangshan Mountains. The geothermal waters possessed the highest reservoir temperature of 299 °C and the largest circulation depth of 2010 m according to various geothermometers. The geothermal waters can produce CaCO3 and SiO2 scaling during vertical and horizontal transport. These achievements can provide a scientific basis for the sustainable development and conservation of the high-temperature geothermal resources in Yangbajing and elsewhere.

A study on the geothermal circulation system of granite: An example from the Lancang area, Yunnan

This study assesses the geothermal water circulation process of a granite geothermal system in the Lancang area, Yunnan. Cycling processes are studied using water chemistry and isotope analysis techniques. The results show that the water chemistry type of the hot springs in Lancang is Na-HCO3, with TDS values ranging from 246 to 724 mg/l. The granite pluton, as the main heat source, has a high radiogenic heat generation rate (4.17 μW/m3 on average). δD and δ18O in Lancang are close to the global atmospheric and local precipitation lines, indicating that geothermal water originates from atmospheric precipitation. Moreover, the mountainous area from 1295.3 to 1624.5 m above sea level is the main precipitation recharge area. In addition, the main ions of geothermal water mainly come from the dissolution, weathering, and cation exchange of silicate minerals in granite, and Ca2+ and Mg2+ in the water are exchanged with Na+ and K+ in the reservoir, significantly increasing the Na+ and K+ concentrations in the water. The reservoir temperatures are 126.60 °C to 151.32 °C based on the SiO2 geothermometer, and the depths range from 2283.05 to 4024.59 m. The NW- and NE-oriented fault system in Lancang serves as a channel for geothermal water to exit the ground and form hot springs; this water is also mixed with cold water during upwelling, and the mixing ratios are 63 %-84 %. Finally, the model of geothermal water circulation in the Lancang is established.

Lithium extraction from typical lithium silicate ores by two bacteria with different metabolic characteristics: Experiments, mechanism and significance

Microorganisms obtain inorganic nutrients or energy from specific minerals to selectively weather minerals, but few studies on the differences in metabolic components of different functional bacteria lead to different weathering effects. This study evaluated the leaching effects of two bacteria with distinct metabolic characteristics on lithium silicate minerals with different structures. We aimed to understand the microscopic mechanism of crystal destruction of lithium silicate minerals with different structures under the action of microorganisms. The results showed that the metabolites produced by an acid producing silicate strain Raoultella sp. Z107 (strain Z107) had a high content of organic acids, among which lactic acid was up to about 11 g/L. Bacillus mucilaginosus 21,699 (strain BM) secreted capsular polysaccharide with a high content of 14.84 mg/L. The metabolic activities of the two strains were significantly different. Through the analysis of the leaching residue, it was found that the lithium silicate minerals were acid etched, interlayer domains expanded, crystallinity decreased, and metal bonds were broken under the action of bacteria. The dissolution of lithium silicate minerals by bacteria is a combination of bacterial adsorption, organic acid corrosion, and complexation of small molecular organic acids and macromolecular polymers with metal ions. The acid erosion and complexation effects of organic acids are greater than the single complexation of capsular polysaccharides, and the layered lepidolite is more likely to be decomposed by the weathering of bacterial metabolites than the chain structure spodumene. These results indicate that the diversity of metabolic activity of bacteria from different sources and the sequence and decomposition mechanism of metal ions released from minerals after lattice destruction are also different. Microorganisms decompose minerals for energy and nutrients, and eventually become the main players in the transformation of elements in biogeology.