Major Ion Chemistry Research Articles

Appraisal of contamination, hydrogeochemistry, and Monte Carlo simulation of health risks of groundwater in a lithium-rich ore area.

This study incorporated hydrogeochemical facies, the entropy-weighted water quality index (EWQI), multivariate statistics, and probabilistic human exposure assessment to investigate hydrogeochemistry, analyze groundwater quality, and estimate potential risks to human health in a lithium-rich ore area (Jadar River basin, Serbia). The findings designated the Ca·Mg-HCO3 hydrogeochemical type as the predominant type of groundwater, in which rock weathering and evaporation control the major ion chemistry. Due to the weathering of a lithium-rich mineral (Jadarite), the lithium content in the groundwater was very high, up to 567mg/L, with a median value of 4.3mg/L. According to the calculated EWQI, 86.4% of the samples belong to poor and extremely poor quality water for drinking. Geospatial mapping of the studied area uncovered several hotspots of severely contaminated groundwater. The risk assessment results show that groundwater contaminants pose significant non-carcinogenic and carcinogenic human health risks to residents, with most samples exceeding the allowable limits for the hazard index (HI) and the incremental lifetime cancer risk (ILCR). The ingestion exposure pathway has been identified as a critical contaminant route. Monte Carlo risk simulation made apparent that the likelihood of developing cancerous diseases is very high for both age groups. Sensitivity analysis highlighted ingestion rate and human body weight as the two most influential exposure factors on the variability of health risk assessment outcomes.

Major Ion Chemistry of Surface Water and Its Controlling Factors in Ebinur Lake Basin

The sustainable development of arid regions is significantly constrained by the availability of water resources, which play a crucial role in this context. It is necessary to deeply investigate and analyze the hydrochemical characteristics and major ion sources. This study, which was based on data from 183 water samples collected from the Jinghe River Basin, provided a comprehensive analysis of the river water hydrochemistry. The results show that the average TDSs (total dissolved solids) was measured at 49.8 mg·L−1. HCO3− (82.4%) and Ca2+ (77.1%) were the ions present in the highest abundances. The river water was classified as the HCO3−-Ca2+ hydrochemical type. The Gibbs diagrams indicated that the ion composition was primarily influenced by rock weathering. Additionally, the Na-normalized molar ratio diagrams suggested that the chemical composition was primarily governed by the weathering and dissolution of silicate rocks, while the carbonate rock dissolution played a lesser role. This study demonstrates a critical aspect of water resources quality evaluation, which is of great significance for the sustainable development, utilization and environmental protection of regional water resources.

Investigation of hydrochemical characteristic, water quality and associated health risks of metals and metalloids in water resources in the vicinity of Akamkpa quarry district, southeastern, Nigeria

Quarrying of rock aggregates generates produced water that, if not handled properly will be a source of pollution for nearby water bodies, thus affecting the chemistry of the water. This study examined the chemistry, impact of quarrying activities on water resources and the health consequences/risks posed by ingestion of the water by humans in the Akamkpa quarry region in southeastern Nigeria. Thirty (30) water samples consisting of pond water, stream water, hand dug wells, and borehole samples were collected and analyzed for their physicochemical parameters using standard methods. The results obtained from the analyses indicated that the water was moderately acidic, fresh, and not salty, with many parameters below the recommended standards with Ca2+, and HCO3− being the dominant ions present in the water resources. Rock weathering processes including silicate weathering as illustrated by hydrochemical facies, cross plots, and Gibbs diagrams are the dominant mechanisms influencing the quality and major ions chemistry of the water resources with minor contributions from dissolution, anthropogenic activities, and ion exchange. Ca-Mg-SO4-Cl and Na–K-HCO3− are the most important water types. Although the water quality index shows that the water is suitable for human use and irrigation, the mean values of As, Cd, Pb, and Se are above the acceptable limits. Additionally, the calculated contamination factor revealed the water resources are moderate to highly contaminated by As, Cd, Cr, Mo, Pb, Sb, and Se, and are therefore unsuitable for consumption with regards to these parameters. However, the residual sodium carbonate and water hazard index (WHI) values showed that 38% to 90% of sites in the quarry area were unsuitable for cultivation, 10–30% were in the low to medium impact category, and 60% were classified as risky and are from high to very high impact category. A non-cancer study of inhabitants living in the vicinity of the quarry area indicated that 6.7% of the sites have values greater than one, indicating that it may endanger the health of the people. Therefore, constant monitoring of the water quality is recommended as long-term use of contaminated water can harm humans, plants, and soils.

Understanding arsenic and manganese enrichment in the aquifers of the Ghaghara river basin, Middle Gangetic Plain (MGP), India: A multivariate statistical, compositional data analysis (CoDA), and receptor model approach

The focus of this study was to comprehend the spatial distribution, source apportionment, evaluation of natural background level (NBL), and mobilization mechanisms of arsenic (As) and manganese (Mn) in the Ghaghara river basin, located in the middle Gangetic plain (MGP) of India. A combination of analytical tools was employed, including multivariate statistical analysis (MSA), correlation analysis, and receptor models such as positive matrix factorization (PMF) and principal component analysis-multi linear regression (PCA-MLR). Taking into consideration the compositional constraints of the geochemical data, compositional data analysis (CoDA) methods were applied on the raw data prior to the correlation analysis and MSA. The results of MSA, correlation analysis and receptor models showed that major ion chemistry and As, Mn enrichment in groundwater were largely controlled by carbonate weathering, Fe and Mn oxyhydroxides dissolution. Anthropogenic activities, such as the infiltration of dissolved organic matter-rich water from local surface water bodies used as dumping sites and the infiltration of fertilizer-rich water from agricultural lands, were found to notably impact the groundwater geochemistry and release of As in the research area. The lower NBL of As (5.92 μg/L) compared to its mean concentrations (17.9 μg/L) in the study area also indicated that the rate of As release in groundwater through natural processes was comparatively low but various anthropogenic activities operating in the study region possibly acted as a trigger for the mobility of As from the mineral phases of the subsurface sediments. This study also highlighted the significance of applying CoDA techniques on geochemical data prior to statistical analysis, and the importance of receptor models, to better understand the nature and contribution of various natural and anthropogenic processes governing the hydrochemistry of groundwater in the alluvial aquifers.

Groundwater recharge sources and mechanisms in the Ethiopian central Afar rift: Insights from isotopic and hydrogeochemical tracers.

Groundwater flow and recharge mechanisms in the central Afar rift and the associated western marginal grabens and Northwestern Plateau (NWP) are poorly understood because of the complex geology and spatial heterogeneity in the aquifer systems. The major aquifers in the region include the Oligocene and Pliocene to recent volcanics and recent alluvio-lacustrine sediments. We employed hydrogeochemical, stable isotopes of water (18O and 2H), and geological structures insights to identify groundwater recharge sources and mechanisms, aiming to develop a representative conceptual groundwater flow model. Water samples from groundwater and surface water were collected based on lithological/aquifer variation and geomorphological setup for isotope and hydrochemical analysis. Findings reveal distinct isotopic differences between the deep (>350 m) and shallow groundwater systems of the Afar rift, with deep systems showing relative isotopic depletion, indicating varying recharge sources. The deep groundwater exhibited a similar isotopic signature to that of the marginal grabens and NWP. The distribution of major ion chemistry and electric conductivity (EC) of groundwaters from the western plateau to the Afar rift show significant spatial variability. However, in some corridors of western parts of the rift, there is a clear geochemical evolution along the flow paths inferring groundwater flow continuity between aquifers. The results revealed the existence of preferential deep groundwater recharge from the NWP through the highly fractured linking zones, interacting fault zones in between the marginal grabens, to the deeper volcanic aquifers of the central Afar rift. The proposed groundwater flow model of this study illustrates the deep groundwater flow from the NWP to the Afar rift is primarily directed by the orientations of the faulted marginal grabens and the highly fractured interacting zones. This model is pivotal for understanding groundwater dynamics in similar continental rift environments, offering insights for effective groundwater management.

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.

Characterization of The Interaction Between Surface Water and Groundwater Using Major Ion Chemistry and Stable Isotopes Northwest Sinai Egypt

Characterization of The Interaction Between Surface Water and Groundwater Using Major Ion Chemistry and Stable Isotopes Northwest Sinai Egypt

Geochemical processes, salinity sources and utility characterization of groundwater in a semi-arid region of Iraq through geostatistical and isotopic techniques.

Identifying factors contributing to water salinity is paramount in efficiently managing limited water resources in arid environments. The primary objective of this study is to enhance understanding regarding the hydrochemistry, source, and mechanism of water salinity, as well as to assess the suitability of water for various uses in southern Iraq. The groundwater samples were collected from water wells and springs and analyzed for major cations and anions along with stable isotopes (δ18O and δ2H) to accomplish the objective. The analysis of major ion chemistry, hydrochemical techniques, principal component analysis (PCA), and isotope signatures were adopted to determine the primary factors contributing to water mineralization. The study inferred that evaporation and geological processes encompassing water-rock interactions, such as dissolution precipitation and ion exchange, were key processes. The stable isotope analysis revealed that the water originated from meteoric sources and underwent significant evaporation during or before infiltration. The utility assessment of water samples indicates that most samples are not appropriate for consumption and are significantly below the established standards for potable water. In contrast, a significant portion of the groundwater samples were found to meet the criteria for irrigation suitability by adopting Wilcox and the US Salinity Laboratory criteria. The groundwater could be considered for irrigation with proper salinity control management. Overall, this study has significantly improved the understanding of the hydrogeochemical regimes and acts as a first step toward the sustainable utilization of water resources.

Seasonality of hydrogeochemical evolutions and isotopic variabilities (δ18O, δ2H and d-excess) in the surface water as well as groundwater from tropical central-south Mexico

Due to adverse impact of the global warming on hydrological resources, we intended to document the hydrogeochemical evolutions of surface and groundwater at tropical central-south Mexico in terms of seasonality of rock-water interaction, precipitation/evaporation variation and moisture source by evaluating the major ion chemistry in Piper and Gibbs plots, Durov diagram and through estimation of the chloro-alkaline indices as well as assessing the stable isotope compositions (δ18O and δ2H) in samples from different seasons of a year. Surface water of the Lake Coatetelco shifted from mostly Ca–Mg–HCO3 facies in wet summer-autumn to Na–HCO3–Cl facies in the dry spring due to elevated Na, Cl and HCO3. Greater evaporation in spring led to a maximum δ18O enrichment of ca.7‰ compared to the other seasons, and much depleted deuterium excess (−40.92‰ to −39.20‰). Interaction of the lake water with subsurface carbonate lithologies, and comparable isotopic compositions reflected the enhanced interaction between the surface water body and aquifers in the wet autumn. Effect of seasonality, however, was unclear on the groundwater facies, and its heterogenous composition (Ca–Mg–HCO3, Na–HCO3–Cl and Na–HCO3) reflected the interactions with different lithologies. Fractionations in isotope compositions of the groundwater were caused from recharge at different elevations, seasonality of moisture sources and moisture recycling. The water-mineral saturation index was an efficient proxy of seasonality as the lake water and groundwater (avg SIcalcite > 0.5) of the dry autumn were saturated with calcite. This vital information about carbonate precipitation, pCO2 and chemical facies would be useful for the better interpretation of paleoclimate archives in this region.

Large-scale groundwater flow and sedimentary diagenesis in continental shelves influence marine chemical budgets

The major ion chemistry of the ocean has been assumed to be controlled by river input, hydrothermal circulation at mid-ocean ridges, carbonate production, and low-temperature alteration of seafloor basalt, but marine chemical budgets remain difficult to balance. Here we propose that large-scale groundwater flow and diagenetic reactions in continental shelf sediments have been overlooked as an important contributor to major ion budgets in the ocean. Based on data synthesized from 17 passive margin basins, continental shelves contribute fluid exchanges comparable to hydrothermal circulation at mid-ocean ridges. Chemical exchange is similarly significant, indicating removal of Mg2+ from the oceans at rates similar to mid-ocean ridge convection. Continental shelves likely contribute Ca2+ and K+ to the oceans at rates that, in combination with low-temperature basalt alteration, can close current budget deficits. Flow and reaction in continental shelf sediments should be included in a new generation of studies addressing marine isotope budgets.

Using multivariate statistics to link major ion chemistry changes at karst springs to agriculture

Agricultural contamination is a pervasive problem in karst landscapes that negatively impacts groundwater quality, and subsequently harms hydraulically connected springs and associated ecosystems. While most research on agricultural contamination in karst aquifers has focused on nitrate, agricultural operations also alter major ion chemistry in groundwater, which can have significant implications on water rock interactions, geochemical interpretability, and enrichment of harmful contamination. Additionally, recent evidence has questioned the singular role of nutrient enrichment on aquatic ecosystem degradation, thus prompting further investigation into the broader extent of agricultural contamination for improved water quality restoration. In karst aquifers, quantifying the disruption of groundwater quality from agricultural contamination at springs can be challenging as major ions associated with agricultural contamination may be conflated with natural processes and interpretation further compounded by complex flow dynamics. These factors can render traditional statistical methods inadequate for identifying more comprehensive groundwater quality disruptions. To overcome these challenges, we use principal component analysis to classify the major ion covariance signature of agriculturally impaired and unimpaired groundwater and develop a new impairment metric to characterize the relative major ion impairment from agriculture to karst spring water quality. We apply our method to a primarily rural region in northern Florida whereby major ion chemistry has been changing over the last several decades. Our results identify a significant difference in major ion covariance structure between agriculturally impaired and unimpaired groundwater which is exploited to directly link major ion changes at karst springs to agriculture via relating a derived impairment metric to measured nitrate. Our newly developed method is easy to apply and can be used to identify more comprehensive contamination from pollutant sources and prioritize relative water quality restoration.

Geochemical evolution of geothermal waters in the Pearl River Delta region, South China: Insights from water chemistry and isotope geochemistry

The Pearl River Delta (PRD) region in South China is abundant of geothermal water resources whereas geochemical evolution of the geothermal water is still poorly understood. In this study, geothermal water is sampled to investigate the provenance of CO2 and sulphate, residence time, recharge elevation, circulation depth, and water-interaction processes by analyzing chemistry of major ions and isotope geochemistry. The range of δ13C and content of bicarbonate reveal multiple sources of soil CO2, carbonate rocks, and small amounts of mantle CO2. The δ34S ratio and sulphate concentration are attributed to evaporites dissolution, input of atmospheric sulphur, seawater intrusion, and oxidation of pyrite. The residence time of up to 21.01 ka for geothermal water likely suggests the earliest precipitation recharge during the Late Pleistocene. Mountains or/and hills at an altitude of 300–760 m in north PRD region are currently the major recharge areas for the geothermal water which can circulate at the depths of up to 3000–4800 m along regional structures. The isotopic and hydrochemical analysis confirms that extensive water interaction with silicate rock, carbonate rock and evaporite, evaporation-crystallization process, and cation exchange are the key mechanisms that control the geochemical evolution of geothermal water in the PRD geothermal system.

Human Health Risk Assessment through Depiction of Major Ion Chemistry of Groundwater from Part of Balaghat District (MP), Central India

The key interpretations on the study concerning the human health risk appraisal and hydrogeochemical environment of major ions (cations and anions) of the groundwater samples from the part of Balaghat District (MP) latitude 21°31’42”: 2143’11” N and longitude 79°50’ 30”: 80°11’30”E., Central India are presented here. The pH and EC values were found to grade between 7.3 to 8.6 and 50 to 5080 µS/cm, unraveling the alkaline nature of groundwater and numerous phases of processes in groundwater characterization. The ion exchange along with the solubilization processes during the rock-water interaction undoubtedly represents the geogenic as well as non-geogenic sources for the salinity in the groundwater of the study area. The Ca2+ is predominant over the other cations, wherein the abundance succession of cations is Ca2+ > Na+ > Mg2+ > K+ . The HCO3 - predominates over the other anions with the abundance succession as - HCO3 - > Cl- > NO3 - > SO4 2- > F- . The concentrations of the cations and the anions have been subjected to Aquachem4 software to get the Piper trillinear diagram for the groundwater samples of the study area and it has been found that the alkaline earths (Ca + Mg) exceed the alkalis (Na + K). The three major facies evaluated after the analysis from the study area are Mg-HCO3 (75%), Na-HCO3 (16%) and Ca-HCO3 (9%). The total health hazard quotient (THI) values due to NO3 - content range from 0.026 to 6972 mg/kg/day for the adult and from 0.034 to 1002.7 mg/kg/day for children. Similarly, the health hazard quotient (THI) values due to Fconcentration ranges from 0.01 to 0.19 mg/kg/day and from 0.02 to 0.52 mg/kg/day for adult and children respectively. Thus, the study points out that the children are more susceptible to the non-carcinogenic risk than to adults and may pose undesirable health effects.

Hydrochemical Characteristics of Groundwater in and around the Peenya Industrial Area in Bengaluru City

The present study aims to use the Water Quality Index (WQI) modeling method to know about groundwater hydrochemistry and drinking suitability in and around (5 km) the Peenya industrial area/estate in Bengaluru city. For this research study, 116 bore well samples were collected and examined for the pre (dry) and post (wet) monsoon seasons in 2021, following APHA standard procedures. According to the BIS standard, the TH, Ca, Mg, NO3, and TDS exceed the desirable limits in both seasons. The water quality examination data shows that TDS concentration is found to be higher above the desired limit (500 mg/l) during the pre- (63%) and post- (45%) monsoon seasons. Furthermore, 55% (pre-monsoon) and 15% (post-monsoon) of the groundwater samples exceed the BIS’s nitrate allowable limit (45 mg/l). Among the analyzed samples, the calcium content in 19% and 20% of samples exceeded the desirable limit (75 mg/l), and magnesium content in 87% and 83% exceeded the desirable limit (30 mg/l) in pre- and post-monsoon seasons. In 95% of samples, TH content exceeded the desirable limit (200 mg/l) in both pre- and post-monsoon seasons. Piper diagram plots were utilized to determine sources of dissolved constituents, rock-water interaction, and other factors that influenced the region’s groundwater composition. Based on hydro-chemical facies the Ca-Mg-HCO3 type of water predominates in the study area during pre (dry) and post (wet)-monsoon seasons of the year 2021. The chemistry of groundwater has deteriorated significantly because of several industrial and anthropogenic activities. The WQI spatial distribution map shows that groundwater quality has the greatest impact in the west and a few places in the north and south regions of the research area. This study was conducted in Bangalore’s Peenya industrial area to determine whether groundwater is suitable for drinking, identify the mechanisms governing groundwater’s geochemistry, and evaluate the effects of an industrial area on groundwater quality. The primary focus of this study is the major ion chemistry in this field.

Evaluation and Interpretation of Legacy Major-Ion Chemistry for the Niobrara River Watershed, Northwestern and Northcentral Nebraska, USA

Evaluation and Interpretation of Legacy Major-Ion Chemistry for the Niobrara River Watershed, Northwestern and Northcentral Nebraska, USA

Impact assessment of long-term high-volume abstraction of groundwater from Palla floodplain aquifers of Delhi, India

The global demand for freshwater resources has universally stressed the groundwater system. This is particularly seen in urban areas like the National Capital Territory (NCT), Delhi where extreme disturbance in the natural flow conditions may result in a variety of complex hydrological crises. To address the issues of uneven water distribution in NCT-Delhi, a detailed assessment was undertaken to formulate a holistic approach to efficiently utilize natural water in the late 1990s and early 2000s, leading to the development of the Palla well field, which has been deemed successful on the water supply front. However, its hydrogeological impact assessment was not fully reviewed until now.In this context, the study presented here aims to assess the impact of the long-term pumping from Palla well field tube wells on the physical and chemical attributes of the hydrogeological system. The experimental investigations revealed that the aquifers have high potential, and can achieve dynamic equilibrium relatively faster, thereby showing resilience to the drastic effects of prolonged pumping. Furthermore, the isotopic signatures revealed varying impacts of recharge associated with given hydrological settings.Additionally, the XRD and SEM-EDS analyses indicate that the sediment-groundwater interaction does not primarily control the major ion chemistry in the younger alluvium. However, iron enrichment in a few groundwater samples was supposedly observed to be a product of the chemical weathering of iron oxides. Overall, the multifaceted investigation provided evidence that there is no major detrimental impact on the groundwater system from the prolonged pumping in the Palla wellfield.

Major Ion Chemistry of Waters and Possible Controls under Winter Irrigation in the Saline Land of Arid Regions

To reduce downstream ecological damage, it is crucial to analyze water and salt sources in saline–alkali farmland drainage and optimize soil salt discharge. This study employs statistical, hydrochemical, and isotope methods to identify controlling factors and characteristics in water bodies during winter irrigation. The results show average TDS values of 0.59, 6.40, and 4.14 g/L for irrigation, phreatic, and drainage water. Irrigation and phreatic water mainly belong to the HCO3-Ca·Mg·Na and Cl·SO4-Na·Mg types. Na+/(Na+ + Ca2+) and Cl−/(Cl− + HCO3−) values suggest the rock–water interaction and evaporation influences in irrigation water, while evaporation primarily controls phreatic water. The main salt types include NaCl, MgSO4, Na2CO3, and CaCO3 for irrigation water and NaCl, MgSO4, Na2SO4, and CaCO3 for phreatic water. These findings lay a research basis for analyzing water and salt sources in farmland drainage during winter irrigation in saline–alkali land.

Understanding the origins of and influences on precipitation major ion chemistry on the Island of O'ahu, Hawai'i.

Precipitation is the primary groundwater source for the Island of O'ahu, Hawai'i, USA, and is an important source of terrestrial nutrients. Since Pacific Islands are particularly vulnerable to the impacts of climate change, they are important venues for studying the controls on and fluctuations in precipitation chemistry. Spatial variations in some of the dissolved rainfall ions can also be of value as natural geochemical tracers in examining surface and groundwater flow. This study collected and chemically analyzed bulk precipitation from 20 sites across the Island of O'ahu approximately quarterly between April 2018 and August 2021. The new precipitation chemistry data were integrated with previously published precipitation data to characterize major ion composition and examine the atmospheric processes controlling inorganic ion deposition. Linear regression and multivariate analysis were used to quantify the relationships among major ions and to assess the impacts of various environmental and meteorological factors on precipitation chemistry. Ordinary kriging and inverse distance weighted interpolations were conducted to help visualize spatial variations in major ion deposition. The results clearly indicate that ocean sea spray is the primary driver of precipitation inorganic chemistry, with marine sea salt aerosols accounting for more than 90% of the measured ion load. However, they also show that various weather patterns and nutrient sources impact inorganic deposition. Most notably, upper atmospheric transport of Asian continental dust during Hawaiian wet seasons, Ca2+ from local sedimentary deposits, and anthropogenic K+ from agricultural activity appear to be substantial non-marine deposition sources. This study synthesizes data from multiple sources into the most spatially and topographically diverse precipitation collector network on O'ahu to date. The findings from this effort help establish a baseline for assessing future fluctuations in inorganic ion deposition and lay important groundwork for examining connections between precipitation and groundwater chemistry within the study area.

Sampling frequency, load estimation and the disproportionate effect of storms on solute mass flux in rivers

Riverine discharge (Q) and dissolved concentrations (C) dictate solute mass export from watersheds. Commonly Q is tracked at a much higher frequency than C for most major solutes, leading to the necessity of load estimation algorithms which are often based on sparse data. The result is that the disproportionate effects of short-duration events (e.g., storms) on solute mass fluxes are poorly known. Here we use novel lab-in-the-field instrumentation to compare high temporal-resolution (∼30 min to 7 h) datasets of major ion chemistry collected over a year of continuous monitoring in three watersheds ranging over four orders of magnitude in drainage area. In these diverse settings, we quantify the errors associated with common load estimation algorithms and reduced sampling frequencies. When sample frequencies are coarsened, the mass flux of solutes which are diluted by storm events (i.e., Ca2+, Mg2+, Na+, Cl− and SO42−) are systematically overestimated, while nutrients which become mobilized by these events (K+ and NO3−) are underestimated. This is most pronounced in the largest river, and strongly tied to the increasing likelihood that storm events are missed as sampling frequencies decrease. Coarsening our high-resolution data to monthly sampling frequency yields an average overestimate of 8 % for Na+ and an average underestimate of 32.5 % for K+ across the three watersheds, illustrating clear implications for estuary and coastal water eutrophication, chemical weathering budgets, and agricultural land management practices. SynopsisA new ‘lab-in-the-field’ technology produces continuous high-frequency records of the full suite of major ions in rivers. These data highlight the disproportionate effect of large storms on catchment solute exports and the error associated with temporally coarse monitoring.

Spatial distribution of drinking and irrigation water quality in different climatic zones of Baluchistan, Pakistan.

Baluchistan's water profile was developed by dividing it into seven zones (Northern Highlands-NH, Southern Highlands-SH, Quetta Valley-QV, Desert-D, Sibbi Plains-SP, Coastal Lasbella-CL, Coastal Gwadar-CG) based on geography, water availability, and climate of the area. A total of 106 water samples were collected from karaiz, spring water, and tube wells. Spatial distribution of EC, TDS, TH, SO42-, Cl-, Na+, and K+ showed an increasing trend in concentration from the highlands towards the desert and coastal zones. For anion, HCO3- is predominant in NH, SH, and QV, Cl- in D, CL, and CG and only SO42- in SP, whereas the cationic trend in overall zones is Na+>Ca2+>Mg2+>K+. In the NH, SH, QV, and SP zones, the physicochemical parameters met the drinking water quality guidelines; however, D, CL, and CG exceeded in almost all quality parameters. Furthermore, the drinking water quality index (WQI) shows excellent to good water quality in NH, SH, QV, and D zones, while CL and CG fall in poor to unsuitable water classes. In terms of hydrogeochemical facies, maximum water samples from NH fall in Ca-Mg-HCO3, and SH, QV, and SP in Ca-Mg-Cl type, where major ion chemistry is controlled by rock-weathering, while D, CL, and CG fall in the NaCl type, where evaporation is dominant. Similarly, irrigation water quality parameters (EC, SAR, RSC, Na%, MH%, PI, SSP, and KR) reveal that NH, SH, QV, and SP have suitable water for irrigation, and D, CL, and CG require proper treatment. Additionally, USSL and Wilcox's diagrams indicated that NH, SH, QV, and SP have "excellent to permissible"; however, D, CL, and CG have "permissible to unsuitable" class water, requiring special management practices. Consequently, appropriate control measures and targetedwater purification programmes should be implemented to protect the publichealth and sustainability of water resources inBaluchistan.