Geothermal solute flux monitoring and the source and fate of solutes in the Snake River,Yellowstone National Park,WY

The combined geothermal discharge from over 10,000 features in Yellowstone National Park (YNP) can be can be estimated from the Cl flux in the Madison, Yellowstone, Falls, and Snake Rivers. Over the last 30 years, the Cl flux in YNP Rivers has been calculated using discharge measurements and Cl concentrations determined in discrete water samples and it has been determined that approximately 12% of the Cl flux exiting YNP is from the Snake River. The relationship between electrical conductivity and concentrations of Cl and other geothermal solutes was quantified at a monitoring site located downstream from the thermal inputs in the Snake River. Beginning in 2012, continuous (15 min) electrical conductivity measurements have been made at the monitoring site. Combining continuous electrical conductivity and discharge data, the Cl and other geothermal solute fluxes were determined. The 2013–2015 Cl fluxes (5.3–5.8 kt/yr) determined using electrical conductivity are comparable to historical data. In addition, synoptic water samples and discharge data were obtained from sites along the Snake River under low-flow conditions of September 2014. The synoptic water study extended 17 km upstream from the monitoring site. Surface inflows were sampled to identify sources and to quantify solute loading. The Lewis River was the primary source of Cl, Na, K, Cl, SiO₂, Rb, and As loads (50–80%) in the Snake River. The largest source of SO₄ was from the upper Snake River (50%). Most of the Ca and Mg (50–55%) originate from the Snake Hot Springs. Chloride, Ca, Mg, Na, K, SiO₂, F, HCO₃, SO₄, B, Li, Rb, and As behave conservatively in the Snake River, and therefore correlate well with conductivity (R² ≥ 0.97).     

Arsenic and fluoride in the upper madison river system: Firehole and gibbon rivers and their tributaries,yellowstone national park,wyoming, and southeast montana

Chemical analyses of 21 water samples from the Firehole and Gibbon Rivers, which combine to form the Madison River, gave arsenic and fluoride values above the Environmental Protection Agency Interim Primary Drinking Water maximum contaminant levels (0.05 mg/l arsenic and 2.0 mg/l fluoride). On 18 October, 1975, during a period of moderate flow (16,600 l/s), the Madison River at West Yellowstone contained 0.23 mg/l arsenic and 6.2 mg/l fluoride. Below Hebgen Lake the Madison River during periods of high flow (56,000 liter/s at West Yellowstone and 708,000 liter/s below Hebgen Lake) would contain 0.05 mg/l arsenic at both stations and 1.5 and 4.0 mg/l fluoride at West Yellowstone and below Hebgen Lake, respectively. The strong correlations of arsenic and fluoride with other chemical constituents of the river water at the sampling sites demonstrate the conservative nature of each element after it reaches the Madison River system. Calculations indicate that water from three sampling sites is above saturation with respect to fluorite.     

Solute geothermometry of springs and wells of the Los Azufres and Las Tres Vírgenes geothermal fields,Mexico

Subsurface reservoir temperatures of two important Mexican geothermal systems (Los Azufres and Las Tres Vírgenes) were estimated by applying all available solute geothermometers for 88 and 56 chemical data measurements of the spring waters and fluids of the deep geothermal wells, respectively. Most of the chemical data for spring water of these two geothermal fields are for HCO₃ water, followed by SO₄ and Cl types. For the Los Azufres geothermal field (LAGF), the reservoir temperatures estimated by Na-K geothermometers for springs of HCO₃ and SO₄ waters, and by Na-Li and Li-Mg geothermometers for Cl water, are close to the average bottom-hole temperature (BHT) of the geothermal wells. However, all reservoir temperatures for spring waters from the Las Tres Vírgenes geothermal field (LTVGF) estimated by all solute geothermometers indicated significantly large differences (low temperatures) compared to the BHT. Evaluation of inferred reservoir temperatures for spring waters of the LAGF and LTVGF suggests that not all springs nor all solute geothermometers provide reliable estimation of the reservoir temperatures. Even though chemical equilibrium probably was not achieved in the water–rock system, Na-K geothermometers for HCO₃ water (peripheral water mainly of meteoric origin with little geothermal component) and SO₄ water (geothermal steam heated) and Na-Li and Li-Mg geothermometers for Cl-rich spring water (fully mature geothermal water) of the LAGF indicated reservoir temperatures close to the BHT. However, in comparison with the geothermometry of spring water of the LAGF and LTVGF, fluid measurements from geothermal wells of these two fields indicated reservoir temperatures in close agreement with their respective BHTs. For the best use of the solute geothermometry for spring water, it is advisable to: (1) chemically classify the springs based on water types; (2) identify and eliminate the discordant outlier observations by considering each water type as a separate sampled population; (3) apply all available solute geothermometers employing a suitable computer program such as SolGeo instead of using some specific, arbitrarily chosen geothermometers; and (4) evaluate the temperatures obtained for each solute geothermometer by considering the subsurface lithology, hydrological conditions, and BHTs or static formation temperatures whenever available.     

天津市蓟县系雾迷山组地热流体地球化学特征

蓟县系雾迷山组是天津地区最重要的基岩裂隙型热储层。通过对天津市平原区不同构造单元的70组蓟县系雾迷山组地热流体样品的水化学测试,从其化学类型、特殊组分、热储温度及地热水成因等方面进行分析研究。结果表明,流体化学类型北部以HCO_3·SO_4-Na、HCO_3·SO_4·Cl-Na为主,往南变为Cl·HCO_3-Na、Cl·HCO_3·SO_4-Na、Cl·SO_4·HCO_3-Na为主,南部为Cl·SO_4-Na为主;地热流体中的氟、偏硅酸、偏硼酸、温度均达到了"有医疗价值浓度"或"命名矿水浓度"标准;由于雾迷山组地热流体水-岩之间未达到离子平衡状态,K-Mg温标不适用于本地区热储温度的计算,采用玉髓温标来预测热储温度的方法比较适用于本地区的热储。通过成因分析可知该热储属于贫溴的含岩盐地层溶滤水,具有陆相沉积水的特征。     

A linear regression model (LRM) for groundwater chemistry in and around the Vaniyambadi industrial area, Tamil Nadu, India

A linear regression model in conjunction with cluster analysis was applied to the groundwater quality parameters for the Vaniyambadi industrial area, Tamil Nadu, India. These physico-chemical parameters were collected from 25 wells by intensive groundwater sampling conducted during January 2010. All the major ions, pH and electrical conductivity were analyzed. The abundances of cations were in the order of Na 相似文献   

Geochemical constraint on origin and evolution of solutes in geothermal springs in western Yunnan,China

Geothermal resources are very rich in Yunnan, China. However, source of dissolved solutes in geothermal water and chemical evolution processes remain unclear. Geochemical and isotopic studies on geothermal springs and river waters were conducted in different petrological-tectonic units of western Yunnan, China. Geothermal waters contain Ca–HCO₃, Na–HCO₃, and Na (Ca)–SO₄ type, and demonstrate strong rock-related trace elemental distributions. Enhanced water–rock interaction increases the concentration of major and trace elements of geothermal waters. The chemical compositions of geothermal waters in the Rehai geothermal field are very complicated and different because of the magma chamber developed at the shallow depth in this area. In this geothermal field, neutral-alkaline geothermal waters with high Cl, B, Li, Rb Cs, As, Sb, and Tl contents and acid–sulfate waters with high Al, Mn, Fe, and Pb contents are both controlled by magma degassing and water–rock interaction. Geothermal waters from metamorphic, granite, and sedimentary regions (except in the Rehai area) exhibit varying B contents ranging from 3.31 mg/L to 4.49 mg/L, 0.23 mg/L to 1.24 mg/L, and <0.07 mg/L, respectively, and their corresponding δ¹¹B values range from −4.95‰ to −9.45‰, −2.57‰ to −8.85‰, and −4.02‰ to +0.06‰. The B contents of these geothermal waters are mainly controlled by leaching host rocks in the reservoir, and their δ¹¹B values usually decrease and achieve further equilibrium with its surrounding rocks, which can also be proven by the positive δ¹⁸O-shift. In addition to fluid–rock reactions, the geothermal waters from Rehai hot springs exhibit higher δ¹¹B values (−3.43‰ to +1.54‰) than those yielded from other areas because mixing with the magmatic fluids from the shallow magma. The highest δ¹¹B of steam–heated waters (pH 3.25) from the Zhenzhu spring in Rehai is caused by the fractionation induced by pH and the phase separation of coexisting steam and fluids. Given the strong water–rock interaction, some geothermal springs in western Yunnan show reservoir temperatures higher than 180 °C, which demonstrate potential for electricity generation and direct-use applications. The most potential geothermal field in western Yunnan is located in the Rehai area because of the heat transfer from the shallow magma chamber.     

Arsenic and antimony in geothermal waters of Yellowstone National Park,Wyoming, USA

A total of 268 thermal spring samples were analyzed for total soluble As using reduced molybdenum-blue; 27 of these samples were also analyzed for total Sb using flame atomic absorption spectrometry. At Yellowstone the $\text{Cl}\text{As}$ atomic ratio is nearly constant among neutral-alkaline springs with Cl > 100 mg L^?1, and within restricted geographic areas, indicating no differential effects of adiabatic vs. conductive cooling on arsenic. The $\text{Cl}\text{As}$ ratio increases with silica and decreases with decreasing $\text{Cl}\text{ΣCO}{}_3$; the latter relationship is best exemplified for springs along the extensively sampled SE-NW trend within the Lone Star-Upper-Midway Basin region. The relationship between $\text{Cl}\text{As}$ and $\text{Cl}\text{ΣCO}{}_3$ at Yellowstone suggests a possible rock leaching rather than magmatic origin for much of the Park's total As flux. Condensed vapor springs are low in both As and Cl. Very high $\text{Cl}\text{As}$ ratios ( > 1000) are associated exclusively with highly diluted (Cl < 100 mg L^?1) mixed springs in the Norris and Shoshone Basins and in the Upper White Creek and Firehole Lake areas of Lower Basin. The high ratios are associated with acidity and/or oxygen and iron; they indicate precipitation of As following massive dilution of the Asbearing high-Cl parent water.Yellowstone Sb ranged from 0.009 at Mammoth to 0.166 mg L^?1 at Joseph's Coat Spring. Within basins, the $\text{Cl}\text{Sb}$ ratio increases as the $\text{Cl}\text{ΣCO}{}_3$ ratio decreases, in marked contrast to As. Mixed springs also have elevated $\text{Cl}\text{Sb}$ ratios. White (1967) and Weissberg (1969) previously reported stibnite (Sb₂S₃), but not orpiment (As₂S₃), precipitating in the near surface zone of alkaline geothermal systems.     

Groundwater hydrochemistry of a sugarcane cultivation belt in parts of Muzaffarnagar district, Uttar Pradesh, India

The Kali-Hindon is a watershed in the most productive central Ganga plain of India. The whole area is a fertile track with sugarcane being the principal crop. Systematic sampling was carried out to assess the source of dissolved ions, impact of sugar factories and the quality of groundwater. Thirty-six samples were collected covering an area of 395 km². The quality of groundwater is suitable for irrigational purposes but is rich in SO₄ which is not best for human consumption. Graphical treatment of major ion chemistry helps identify six chemical types of groundwater. All possible species such as Na–Cl, K–Cl, Na–HCO₃, Na–SO₄, Ca–HCO₃, Mg–HCO₃, Ca–SO₄ and Mg–SO₄ are likely to occur in the groundwater system. The most conspicuous change in chemistry of groundwater is relative enrichment of SO₄. The interpretation of data reveals that SO₄ has not been acquired through water–rock interaction. The source of SO₄ is anthropogenic. Sugar factories alone are responsible for this potential environmental hazard.     

Geochemistry of sulphate-bearing water of Akra Kaur Dam,Gwadar, Balochistan,Pakistan and its assessment for drinking and irrigation purposes

This paper is an attempt to study the geochemistry of Akra Kaur Dam (AKD) water, north of Gwadar city, southern Balochistan. Representative water samples were collected from AKD reservoir to assess the suitability of water for drinking and agriculture purposes. The major ionic composition is suggestive for freshwater. The average ionic composition demonstrate SO₄ > Ca > Na > Cl > HCO₃ > Mg > K. The plots on Piper diagram reflected Ca–Mg–SO₄ type of water facies. High Ca/SO₄ and Ca/Mg ratios revealed that the water has influence of gypsum dissolution. The negative ratio of chloro-alkaline indices indicated reverse exchange between Ca and Mg in water occurred with Na and K in rocks. The pH, electrical conductivity, total dissolved salts, Ca, Mg, Na, K, HCO₃, Cl and SO₄ concentrations in the dam water were below the permissible limit, however, Na and SO₄ were above the desirable limit, set by the World Health Organization. Important parameters such as residue sodium carbonate, sodium percent, sodium adsorption ratio, permeability index, magnesium content and Kelley’s ratio were calculated to evaluate the suitability of water for irrigation purpose. The result were compared with standard permissible limits and found satisfactory. The health and agriculture hazards of sulphate-bearing water were also discussed.     

Groundwater quality and its suitability for drinking and agricultural use in Chithar River Basin, Tamil Nadu, India

Hydrochemistry of groundwater in Chithar Basin, Tamil Nadu, India was used to assess the quality of groundwater for determining its suitability for drinking and agricultural purposes. Physical and chemical parameters of groundwater such as electrical conductivity, pH, total dissolved solids (TDS), Na⁺, K⁺, Ca²⁺, Mg²⁺, Cl^–, HCO₃^–, CO₃^2–, SO₄^2–, NO^–₃, F^–, B^– and SiO₂ were determined. Concentrations of the chemical constituents in groundwater vary spatially and temporarily. Interpretation of analytical data shows that mixed Ca–Mg–Cl, Ca–Cl and Na–Cl are the dominant hydrochemical facies in the study area. Alkali earths (Ca²⁺, Mg²⁺) and strong acids (Cl^–, SO₄^2–) are slightly dominating over alkalis (Na⁺, K⁺) and weak acids (HCO₃^–, CO₃^2–). The abundance of the major ions is as follows: Na⁺ Ca²⁺ Mg²⁺ > K⁺ = Cl^– > HCO₃^–> SO₄^2– > NO₃^– > CO₃^2– . Groundwater in the area is generally hard, fresh to brackish, high to very high saline and low alkaline in nature. High total hardness and TDS in a few places identify the unsuitability of groundwater for drinking and irrigation. Such areas require special care to provide adequate drainage and introduce alternative salt tolerance cropping. Fluoride and boron are within the permissible limits for human consumption and crops as per the international standards.     

National scale evaluation of groundwater chemistry in Korea coastal aquifers: evidences of seawater intrusion

Pollution of groundwater by seawater intrusion poses a threat to sustainable agriculture in the coastal areas of Korea. Therefore, seawater intrusion monitoring stations were installed in eastern, western, and southern coastal areas and have been operated since 1998. In this study, groundwater chemistry data obtained from the seawater intrusion monitoring stations during the period from 2007 to 2009 were analyzed and evaluated. Groundwater was classified into fresh (<1,500 μS/cm), brackish (1,500–3,000 μS/cm), and saline (>3,000 μS/cm) according to EC levels. Among groundwater samples (n = 233), 56, 7, and 37% were classified as the fresh, brackish, and saline, respectively. The major dissolved components of the brackish and saline groundwaters were enriched compared with those of the fresh groundwater. The enrichment of Na⁺ and Cl⁻ was especially noticeable due to seawater intrusion. Thus, the brackish and saline groundwaters were classified as Ca–Cl and Na–Cl types, while the fresh groundwater was classified as Na–HCO₃ and Ca–HCO₃ types. The groundwater included in the Na–Cl types indicated the effects of seawater mixing. Ca²⁺, Mg²⁺, Na⁺, K⁺, SO₄ ²⁻, and Br⁻ showed good correlations with Cl⁻ of over r = 0.624. Of these components, the strong correlations of Mg²⁺, SO₄ ²⁻, and Br⁻ with Cl⁻ (r ≥ 0.823) indicated a distinct mixing between fresh groundwater and seawater. The Ca/Cl and HCO₃/Cl ratios of the groundwaters gradually decreased and approached those of seawater. The Mg/Cl, Na/Cl, K/Cl, SO₄/Cl, and Br/Cl ratios of the groundwaters gradually decreased, and were similar to or lower than those of seawater, indicating that Mg²⁺, Na⁺, K⁺, SO₄ ²⁻, and Br⁻, as well as Cl⁻ in the saline groundwater can be enriched by seawater mixing, while Ca²⁺ and HCO₃ ⁻ are mainly released by weathering processes. The influence of seawater intrusion was evaluated using threshold values of Cl⁻ and Br⁻, which were estimated as 80.5 and 0.54 mg/L, respectively. According to these criteria, 41–50% of the groundwaters were affected by seawater mixing.     

岷江流域河水主要离子地球化学特征及人类活动影响研究

岷江水流量约为8.9×1010m3/yr,约占长江全流域水量10%。作者对4个监测站监测数据的分析发现,岷江TZ 高于世界河流平均值,具有富HCO3-、Ca2 特征;流域化学剥蚀通量为20.48×106t/yr,约占长江流域的10%;化学剥蚀速率为155.9t/km2.yr。岷江在流经四川盆地时主要离子SO42-、Cl-和Ca2 均已受到了人类活动较为严重的影响,酸雨是SO42-的主要污染来源,Cl的污染来源包括生活和工业废水、化肥和井盐开采,农业生产使用的富Ca化肥应是河流Ca污染源之一。     

A hydrogeochemical approach to evaluate the occurrence and source of salinization in the shallow aquifers of the southeastern Imphal valley in the Indo-Myanmar range of Northeast India

The Imphal valley is an intramontane basin confined within an anticlinorium of several anticlines and synclines in the Disang Group of rocks of Tertiary age. This valley of more than 2 million people is occupied by fluvio-lacustrine deposits of Quaternary age and is located in the central part of the Indo-Myanmar range of Northeast India. The hydrogeochemical parameters of temperature, pH, ORP, TDS, Na, Cl, Br, Ba, B, Sr, Li, δ¹⁸O, HCO₃, K, Mg, Ca, NO₃, PO₄, SO₄ in 173 samples using ion-chromatograph, ICP (AES), ICP (OES), ICP (MS) and 37 dugwells were studied to understand the occurrence and origin of salinization process for the first time. The order of abundance of ions is identified as HCO₃ > Na > Cl > Ca > Mg > K > NO₃ > PO₄ > Sr > Br > B>Ba > Li > SO₄. Five hydrochemical facies (Na–Cl, Ca–Mg–HCO₃, Na–HCO₃, Ca–Mg–HCO₃–Cl and Ca–Mg–Cl) represent the types of waters. The saline-dominated water types (Na–Cl and Na–HCO₃) represent piedmont and the rest of the facies represent alluvial plain and flood plain groundwaters. Durov’s diagram reveales initial and intermediate stages of groundwater evolution. Isotope δ¹⁸O, Gibbs diagram and ions scatter plots suggest evaporation and crystallization processes leading to halite encrustation in the Disang shales. Negative Eh, low NO₃ and the absence of SO₄ indicates reduced condition coupled with rich dissolve organic matters leading to elevation of salts in soils around piedmont where the rock type is exclusively of the Disang shales. Trilinear plot, correlation matrix and water table flow analysis suggest salinization of groundwater originates in piedmont groundwater and disseminates towards alluvial plain and flood plain along the flow path.     

Hydrogeochemistry of coal mine water of North Karanpura coalfields,India: implication for solute acquisition processes,dissolved fluxes and water quality assessment

Mine water samples collected from different mines of the North Karanpura coalfields were analysed for pH, electrical conductivity, total dissolved solids (TDS), total hardness (TH), major anions, cations and trace metals to evaluate mine water geochemistry and assess solute acquisition processes, dissolved fluxes and its suitability for domestic, industrial and irrigation uses. Mine water samples are mildly acidic to alkaline in nature. The TDS ranged from 185 to 1343 mg L^?1 with an average of 601 mg L^?1. Ca²⁺ and Mg²⁺ are the dominant cations, while SO₄ ^2? and HCO₃ ^? are the dominant anions. A high concentration of SO₄ ^2? and a low HCO₃ ^?/(HCO₃ ^? + SO₄ ^2?) ratio (<0.50) in the majority of the water samples suggest that either sulphide oxidation or reactions involving both carbonic acid weathering and sulphide oxidation control solute acquisition processes. The mine water is undersaturated with respect to gypsum, halite, anhydrite, fluorite, aluminium hydroxide, alunite, amorphous silica and oversaturated with respect to goethite, ferrihydrite, quartz. About 40% of the mine water samples are oversaturated with respect to calcite, dolomite and jarosite. The water quality assessment shows that the coal mine water is not suitable for direct use for drinking and domestic purposes and needs treatment before such utilization. TDS, TH, F^?, SO₄ ^2?, Fe, Mn, Ni and Al are identified as the major objectionable parameters in these waters for drinking. The coal mine water is of good to suitable category for irrigation use. The mines of North Karanpura coalfield annually discharge 22.35 × 10⁶ m³ of water and 18.50 × 10³ tonnes of solute loads into nearby waterways.     

Groundwater quality assessment from a hard rock terrain, Salem district of Tamilnadu, India

A total of 162 groundwater samples for three representative seasons were collected from Salem district of Tamilnadu, India to decipher hydrogeochemistry and groundwater quality for determining its suitability for drinking and agricultural proposes. The water is neutral to alkaline in nature with pH ranging from 6.6 to 8.6 with an average of 8.0. Higher electrical conductivity was observed during post-monsoon season. The abundance of major ions in the groundwater was in the order of $ {\text{Na} > \text{Ca} > \text{Mg} > \text{K} = \text{Cl} > \text{HC}}{{\text{O}}_3}\; > \;{\text{S}}{{\text{O}}_4}\; > \;{\text{N}}{{\text{O}}_3} $ . Piper plot reveals the dominance of geochemical facies as mixed Ca–Mg–Cl, Na–Cl, Ca–HCO₃, Ca–Na–HCO₃, and Ca–Cl type. NO₃, Cl, SO₄, and F exceed the permissible limit during summer and post-monsoon seasons. Sodium adsorption ratio was higher during post-monsoon and southwest monsoon season indicating high and low salinity, satisfactory for plants having moderate salt tolerance on soils. Permeability index of water irrespective of season falls in class I and class II indicating water is moderate to good for irrigation purposes. As per the classification of water for irrigation purpose, water is fit for domestic and agricultural purposes with minor exceptions irrespective of seasons.     

Hydrogeochemical assessment of surface and groundwater resources of Korba coalfield,Central India: environmental implications

The present study assesses the impact of coal mining on surface and groundwater resources of Korba Coalfield, Central India. Accordingly, water samples collected from various sources are analyzed for major ions, trace elements, and other mine effluent parameters. Results show that the groundwater samples are slightly acidic, whereas river water and mine water samples are mildly alkaline. Elevated concentrations of Ca²⁺, Na⁺, HCO₃ ^?, and SO₄ ^2? alongside the molar ratios (Ca²⁺+Mg²⁺)/(SO₄ ^2?+HCO₃ ^?) <1 and Na⁺/Cl^? >1 suggest that silicate weathering (water-rock interaction) coupled with ion exchange are dominant solute acquisition processes controlling the chemistry of groundwater in the study area. The overall hydrogeochemistry of the area is dominated by two major hydrogeochemical facies (i.e., Ca–Cl–SO₄ and Ca–HCO₃). Analysis of groundwater and river water quality index (GRWQI) elucidates that majority (82%) of samples are of “excellent” to “good” category, and the remaining 12% are of “poor” quality. Similarly, the effluent water quality index (EWQI) indicates that 6 out of 8 samples belong to excellent quality. Concentration of trace element constituents such as As, Zn, Cu, Cr, and Cd is found to be well within the stipulated limits for potable use, except for Fe, Mn, and Pb. Suitability of water samples for irrigation purpose, established using standard tools like Wilcox and USSL diagrams, reveal “excellent to permissible” category for majority of the samples. The present study also substantiates the effectiveness of the measures implemented for the treatment of mine effluent water.     

Major ion chemistry,weathering processes and water quality assessment in upper catchment of Damodar River basin,India

The chemical characteristics of surface, groundwater and mine water of the upper catchment of the Damodar River basin were studied to evaluate the major ion chemistry, geochemical processes controlling water composition and suitability of water for domestic, industrial and irrigation uses. Water samples from ponds, lakes, rivers, reservoirs and groundwater were collected and analysed for pH, EC, TDS, F, Cl, HCO₃, SO₄, NO_3, Ca, Mg, Na and K. In general, Ca, Na, Mg, HCO₃ and Cl dominate, except in samples from mining areas which have higher concentration of SO₄. Water chemistry of the area reflects continental weathering, aided by mining and other anthropogenic impacts. Limiting groundwater use for domestic purposes are contents of TDS, F, Cl, SO₄, NO₃ and TH that exceed the desirable limits in water collected from mining and urban areas. The calculated values of SAR, RSC and %Na indicate good to permissible use of water for irrigation. High salinity, %Na, Mg-hazard and RSC values at some sites limit use for agricultural purposes.     

Groundwater solute chemistry,hydrogeochemical processes and fluoride contamination in phreatic aquifer of Odisha,India

The work investigates the major solute chemistry of groundwater and fluoride enrichment(F~-) in the shallow phreatic aquifer of Odisha.The study also interprets the hydrogeochemical processes of solute acquisition and the genetic behavior of groundwater F~-contamination.A total of 1105 groundwater samples collected from across the state from different hydro-geomorphic settings have been analyzed for the major solutes and F~-content.Groundwater is alkaline in nature(range of pH: 6.6–8.7; ave.: 7.9) predominated by moderately hard to very hard types.Average cation and anion chemistry stand in the orders of Ca~(2+) Na~+ Mg~(2+) K~+and HCO_3~- Cl~- SO_4~(2-) CO_3~(2-)respectively.The average mineralization is low(319 mg/L).The primary water types are Ca-Mg-HCO_3 and Ca-Mg-Cl~-HCO_3, followed by Na-Cl, Ca-Mg-Cl, and Na-Ca-Mg-HCO_3~-Cl.Silicate-halite dissolution and reverse ion exchange are the significant processes of solute acquisition.Both the geogenic as well as the anthropogenic sources contribute to the groundwater fluoride contamination,etc.The ratio of Na~+/Ca~(2+) 1.0 comprises Na-HCO_3(Cl) water types with F~- 1.0 mg/L(range 1.0–3.5 mg/L)where the F~-bears geogenic source.Positive relations exist between F~-and pH, Na~+, TDS, and HCO_3~-.It also reflects a perfect Na-TDS correlation(0.85).The ratio of Na~+/Ca~(2+) 1.0 segregates the sample population(F~- range: 1.0–4.0 mg/L) with the F derived from anthropogenic sources.Such water types include Ca-Mg-HCO_3(Cl) varieties which are recently recharged meteoritic water types.The F~-levels exhibit poor and negative correlations with the solutes in groundwater.The Na-TDS relation remains poor(0.12).In contrast, the TDS levels show strong correlations with Ca~(2+)(0.91), Mg~(2+)(0.80) and even Cl~-(0.91).The majority of the monitoring points with the anthropogenic sources of groundwater F~-are clustered in the Hirakud Canal Command area in the western parts of the state, indicating the role of irrigation return flow in the F~-contamination.     

河北汤泉地热流体水文地球化学特征及其成因

提要：汤泉位于河北省遵化市西北部,为山前丘陵地貌,地热资源丰富。本文通过对该地区地热流体研究发现：Na⁺、Ca²⁺、K⁺、Mg²⁺与SO^2-₄、HCO^-₃、Cl^-、NO^-₃是该地区地下热水的主要成分,水化学类型主要为SO^2-₄-Na⁺型,属于未污染的天然弱碱性水;流体中F^-含量平均为9.36 mg/l,远高于国家地下水质量标准ⅴ级;可溶性SiO₂的含量可作为地热温标;地热流体总矿化度平均为782.33 mg/l,属于淡水;为中等腐蚀型水,不结碳酸钙垢,无CaSO₄?2H₂O垢和SiO₂垢生成的可能;地热流体属于含岩盐地层溶滤的陆相沉积水;根据氢氧稳定同位素可知,河北汤泉地热流体主要来源于大气降水。     

Hydrogeochemical Characteristics and Groundwater Inrush Source Identification for a Multi‐aquifer System in a Coal Mine

Correct identification of water inrush sources is particularly important to prevent and control mine water disasters. Hydrochemical analysis, Fisher discriminant analysis, and geothermal verification analysis were used to identify and verify the water sources of the multi‐aquifer groundwater system in Gubei coal mine, Anhui Province, North China. Results show that hydrochemical water types of the Cenozoic top aquifer included HCO₃–Na+K–Ca, HCO₃–Na+K–Mg and HCO₃–Na+K, and this aquifer was easily distinguishable from other aquifers because of its low concentration of Na⁺+K⁺ and Cl^–. The Cenozoic middle and bottom aquifers, the Permian fissure aquifer, and the Taiyuan and Ordovician limestone aquifers were mainly characterized by the Cl–Na+K and SO₄–Cl‐Na+K or HCO₃–Cl–Na+K water types, and their hydrogeochemistries were similar. Therefore, water sources could not be identified via hydrochemical analysis. Fisher model was established based on the hydrogeochemical characteristics, and its discrimination rate was 89.19%. Fisher discrimination results were improved by combining them with the geothermal analysis results, and this combination increased the identification rate to 97.3 % and reasonably explained the reasons behind two water samples misjudgments. The methods described herein are also applicable to other mines with similar geological and hydrogeological conditions in North China.