Surface Water Chemistry Research Articles

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.

Water quality and dissolved load in the Chirchik and Akhangaran river basins (Uzbekistan, Central Asia)

Uzbekistan (Central Asia) is experiencing serious water stress as a consequence of altered climate regime, past over-exploitation, and dependence from neighboring countries for water supply. The Chirchik–Akhangaran drainage basin, in the Tashkent province of Uzbekistan, includes watersheds from the Middle Tien Shan Mountains escarpments and the downstream floodplain of the Chirchik and Akhangaran rivers, major tributaries of the Syrdarya river. Water in the Chirchik–Akhangaran basin is facing potential anthropogenic pressure from different sources at the scale of river reaches, from both industrial and agricultural activities. In this study, the major and trace element chemistry of surface water and groundwater from the Chirchik–Akhangaran basin were investigated, with the aim of addressing the geogenic and anthropogenic contributions to the dissolved load. The results indicate that the geochemistry of water from the upstream catchments reflects the weathering of exposed lithologies. A significant increase in Na+, K+, SO42−, Cl−, and NO3− was observed downstream, indicating loadings from fertilizers used in croplands. However, quality parameters suggest that waters are generally suitable for irrigation purposes, even if the total dissolved solid indicates a possible salinity hazard. The concentration of trace elements (including potentially toxic elements) was lower than the thresholds set for water quality by different regulations. However, an exceedingly high concentration of Zn, Mo, Sb, Pb, Ni, U, As, and B compared with the average river water worldwide was observed. Water in a coal fly-ash large pond related to the Angren coal-fired power plants stands out for the high As, Al, B, Mo, and Sb concentration, having a groundwater contamination potential during infiltration. Spring waters used for drinking purposes meet the World Health Organization and the Republic of Uzbekistan quality standards. However, a surveillance of such drinking-water supplies is suggested. The obtained results are indicators for an improved water resource management.

Assessing surface water quality in Hungary’s Danube basin using geochemical modeling, multivariate analysis, irrigation indices, and Monte Carlo simulation

Evaluation of water quality is crucial for managing surface water effectively, ensuring its suitability for human use, and sustaining the environment. In the lower Danube River basin, various methods were employed to assess surface water quality for irrigation, drinking, human health risk purposes and the main mechanism control the surface water chemistry. These methods included water quality indicators (WQIs), complex statistical analyses, geographic information systems (GIS), Monte Carlo simulation, and geochemical modeling. Physicochemical analyses of surface water samples revealed primarily Ca–Mg–HCO3− is the dominant water types. Principal component analysis (PCA), ionic ratios and piper, chloro alkaline index, Chadha, and Gibbs diagrams identified three distinct water characteristics influenced by water-rocks interaction, evaporation, ions exchange, and human activities. The geochemical modeling showed Danube River water’s strong ability to dissolve gypsum, halite, and anhydrite (SI < 0) and precipitate aragonite, dolomite, and calcite with saturation index (SI) value greater than 0 along its flow path. The irrigation water quality index (IWQI = 99.6–107.6), sodium adsorption ratio (SAR = 0.37–0.68), sodium percentage (Na% = 13.7–18.7), soluble sodium percentage (SSP = 12.5–17.5), Potential Salinity (PS = 0.73–1.6), and Residual Sodium Carbonate (RSC = − 1.27–0.58) values were used, mainly indicating acceptable quality with some limitations. Danube River water was unsuitable for drinking based on WQI value (WQI = 81–104). Oral exposure of children to specific components showed a higher hazard index (HI > 1) compared to adults, indicating a 2.1 times higher overall non-carcinogenic risk hazard index. However, Monte Carlo simulation demonstrated negligible iron, manganese, and nitrate health hazards for both age groups. These findings are valuable for water quality management decisions, contributing to long-term resource sustainability.

A case study on topsoil removal and rewetting for paludiculture: effect on biogeochemistry and greenhouse gas emissions from Typha latifolia, Typha angustifolia, and Azolla filiculoides

Abstract. Rewetting drained peatlands for paludiculture purposes is a way to reduce peat oxidation (and thus CO2 emissions) while at the same time it could generate an income for landowners, who need to convert their traditional farming into wetland farming. The side effect of rewetting drained peatlands is that it potentially induces high methane (CH4) emissions. Topsoil removal could reduce this emission due to the removal of easily degradable carbon and nutrients. Another way to limit CH4 emissions is the choice in paludiculture species. In this study we conducted a field experiment in the coastal area of the Netherlands, in which a former non-intensively used drained peat grassland is rewetted to complete inundation (water table ∼ +18 cm) after a topsoil removal of ∼ 20 cm. Two emergent macrophytes with high potential of internal gas transport (Typha latifolia and Typha angustifolia), and a free floating macrophyte (Azolla filiculoides), were introduced and intensive measurement campaigns were conducted to capture CO2 and CH4 fluxes as well as soil and surface water chemistry. Greenhouse gas fluxes were compared with a high-productive peat meadow as a reference site. Topsoil removal reduced the amount of phosphorus and iron in the soil to a large extent. The total amount of soil carbon per volume stayed more or less the same. The salinity of the soil was in general high, defining the system as brackish. Despite the topsoil removal and salinity, we found very high CH4 emissions for T. latifolia (84.8 g CH4 m−2 yr−1) compared with the much lower emissions from T. angustifolia (36.9 g CH4 m−2 yr−1) and Azolla (22.3 g CH4 m−2 yr−1). The high emissions can be partly explained by the large input of dissolved organic carbon into the system, but it could also be caused by plant stress factors like salinity level and herbivory. For the total CO2 flux (including C-export), the rewetting was effective, with a minor uptake of CO2 for Azolla (−0.13 kg CO2 m−2 yr−1) and a larger uptake for the Typha species (−1.14 and −1.26 kg CO2 m−2 yr−1 for T. angustifolia and T. latifolia, respectively) compared with the emission of 2.06 kg CO2 m−2 yr−1 for the reference site. T. angustifolia and Azolla, followed by T. latifolia, seem to have the highest potential for reducing greenhouse gas emissions after rewetting to flooded conditions (−1.4, 2.9, and 10.5 t CO2 eq. ha−1 yr−1, respectively) compared with reference drained peatlands (20.6 t CO2 eq. ha−1 yr−1). When considering the total greenhouse gas balance, other factors, such as biomass use and storage of topsoil after removal, should be considered. Especially the latter factor could cause substantial carbon losses if not kept in anoxic conditions. When calculating the radiative forcing over time for the different paludicrops, which includes the GHG fluxes and the carbon release from the removed topsoil, T. latifolia will start to be beneficial in reducing global warming after 93 years compared with the reference site. For both Azolla and T. angustifolia this will be after 43 years.

Boosting the adsorption capacity and anti-impurity performance of zeolitic imidazolate frameworks for antimony(III) in water through the synthesis of leaf-shaped structures

In recent years, the search for effective antimony adsorption materials has been unyielding. However, the exploration of zeolite imidazolate frameworks (ZIFs) as potential adsorbents, along with the influence of material surface structure and water chemistry on their performance remain under explored. In this study, various molar ratios of Zn2+ and 2-methylimidazole are employed to synthesize three distinct shapes of ZIFs: cube, leaf, and dodecahedron. The experimental outcomes reveal that Leaf-ZIFs, exhibit exceptional adsorption capabilities for Sb(III), the maximum adsorption capacity of Leaf-ZIFs was 57.3 mg g−1. The adsorption kinetics adhere to the pseudo-second-order model, and equilibrium is achieved in approximately 10 h. Additionally, the adsorption isotherm curve is consistent with the Freundlich model. Through comprehensive batch experiments, we thoroughly examined the impact of varying solution pH levels, coexisting ions, and the coexistence of humic acids on the adsorption of Sb(III). The Leaf-ZIFs exhibited remarkable adaptability in neutral, alkaline, and low-concentration heteroionic environments, while demonstrating minimal interference from humic acid present in the solution. Analysis using SEM, XPS, and FTIR techniques revealed that the adsorption mechanism of Leaf-ZIFs primarily involved the partial breakage of the Zn-N bond within the material's structure. This breakage led to the formation of Zn-OH groups, which subsequently reacted with Sb(III) molecules through the -OH groups. The culmination of this process was the formation of Zn-O-Sb bonds, resulting in the effective adsorption of Sb(III) from aqueous solutions.

Intrinsic and extrinsic drivers of organic matter processing along phosphorus and salinity gradients in coastal wetlands

Abstract Climate change is accelerating sea‐level rise and saltwater intrusion in coastal regions world‐wide and interacting with large‐scale changes in species composition in coastal wetlands. Quantifying macrophyte litter breakdown along freshwater‐to‐marine coastal gradients is needed to predict how carbon stores will respond to shifts in both macrophyte communities and water chemistry under changing environmental conditions. To test the interactive drivers of changing species identity and water chemistry, we performed a reciprocal transplant of four macrophyte litter species in seven sites along freshwater‐to‐marine gradients in the Florida Coastal Everglades. We measured surface water chemistry (dissolved organic carbon, total nitrogen and total phosphorus), litter chemistry (% nitrogen, % phosphorus, change in N:P molar ratio, % cellulose and % lignin as proxies for recalcitrance) and litter breakdown rates (k/degree‐day). Direct effects of salinity and surface water nutrients were the strongest drivers of k, but unexpectedly, litter chemistry did not correlate with litter k. However, salinity strongly correlated with changes in litter chemistry, whereby litter incubated in brackish and marine wetlands was more labile and gained more phosphorus compared with litter in freshwater marshes. Our results suggest that litter k in coastal wetlands is explained by species‐specific interactions among water and litter chemistries. Water nutrient availability was an important predictor of breakdown rates across species, but breakdown rates were only explained by the carbon recalcitrance of litter in the species with the slowest breakdown (Cladium jamaicense), indicating the importance of carbon structure, and species identity on breakdown rates. Synthesis. In oligotrophic ecosystems, nutrients are often the primary driver of organic matter breakdown. However, we found that variation in macrophyte breakdown rates in oligotrophic coastal wetlands was also explained by salinity and associated seawater chemistry, emphasising the need to understand how saltwater intrusion will alter organic matter processing in wetlands. Our results suggest that marine subsidies associated with sea‐level rise have the potential to accelerate leaf litter breakdown. The increase in breakdown rates could either be buffered or increase further as sea‐level rise also shifts macrophyte community composition to more or less recalcitrant species.

Solute fluxes in headwater catchments with contrasting anthropogenic impact

Understanding the response of headwater catchments to increasing anthropogenic influences is one of the key issues in hydrological and geomorphological research. Two headwater catchments with contrasting human impacts on the environment were chosen to determine changes in surface water chemistry and solute fluxes. In one catchment, 22 % of the forest area was cleared in 2013 and in the other, 75 % of the arable lands was converted to grassland and forest in the last 25 years. Atmospheric input and solute mass balance were analysed using homogeneity Pettitt test. It seems that in both areas, a very important factor affecting solute fluxes was most likely changes, or lack thereof, in soil erosion. In the partially clear-cut catchment, a small clear-cut area and adequate protection of the soil cover had little effect on the stream water chemistry, and the total solute mass balance remained unchanged during the study period. In this catchment, the more pronounced effect on solute fluxes was using de-icing salts in winter, which contributed to a 62 % increase in total solute flux (mainly by supplying Na+ and Cl−, but also Ca2+, Mg2+ and K+). In a catchment with a decrease in arable lands, there was a 55 % decrease in total solute mass balance (including mass balance of Ca2+, Mg2+, Na+, K+, NH4+, SO4−, NO3−, Cl−) in the stream likely associated with a decrease in soil erosion and fertilization. In both catchments there was a decrease in total monthly atmospheric input (especially in input of NH4+, SO4− and NO3−) of 53 % and 21 %, respectively, over the study period. To summarize, the road salting has increased the amount of transported solutes in the stream and deteriorated surface water chemistry, while the reduction of arable land area has reduced the amount of transported solutes in the stream and improved surface water quality.

Hydrogeochemical characteristics of Thrissur Kole Wetland, Southwest India

ABSTRACT Surface water samples collected from Thrissur Kole wetland (UNSECO-protected Ramsar Site) were analysed for hydrogeochemical characteristics. The objectives of this work were to: (i) study the spatial and seasonal variability in water quality and (ii) analyse the hydrogeochemical characteristics of different water types and suitability status for irrigation. Remarkable season-wise and station-wise variation in salinity was attributed to the mixing of freshwater and seawater. Relatively lower values of pH during post-monsoon were due to the freshwater discharge and mineralisation of organic matter. Besides natural sources, agriculture activities, and droppings from birds also serve as sources of nutrients in the wetland. The average relative abundance of major cations and anions was Cl- > Na+ > Mg2+ > K+ > SO4 2- > HCO3 - > Ca2+. In addition, the contribution of dissolved ions from tidal ingression was established by the dominance of magnesium and sulphate. Based on Piper plot, three major hydro-chemical facies (Ca–Mg-HCO3 type, Ca–Mg-Cl-SO4 type, and Na-K-Cl-SO4 type) were identified. Irrigational suitability of water throughout the wetland was excellent during monsoon as per irrigational water quality indices. Piper plot indicated that the surface water chemistry was controlled by silicate weathering with contribution from seawater ingression and anthropogenic sources.

Role of edaphic, hydrologic, and land cover variables in determining dissolved organic carbon in Missouri (USA) reservoirs and streams

Jones JR, Graham JL, Obrecht DV, Harlan JD, Knowlton MF, Pollard C, Parris J, Thorpe AP. 2024. Role of edaphic, hydrologic, and land cover variables in determining dissolved organic carbon in Missouri (USA) reservoirs and streams. Lake Reserv Manage. 40:177–195. In Missouri, distinct geophysical gradients influence statewide patterns in water quality. Here, we quantify the spatiotemporal variability of dissolved organic carbon (DOC) in reservoirs and streams and the edaphic, hydrologic, and land cover variables that account for cross-system variation. Datasets included statewide inventories collected over decades and studies with greater temporal resolution (n = >6350 DOC measurements). Among reservoirs, the smallest DOC concentration was measured in a spring-fed system within a forested watershed, and the largest was where agricultural biosolids were applied to the land (range 1.0–15.9 mg/L, overall mean 5.8 mg/L). Reservoir values increased from the southern forested Highlands (mean 4.7 mg/L) to the northern agricultural Plains (mean 7.0 mg/L). Stream DOC was similar to reservoir values (overall mean in streams 6.3 mg/L; Highlands mean 4.0 mg/L; Plains mean 6.6 mg/L), despite differences in study design and collection period. Reservoir DOC increased in spring, indicative of allochthonous loading, with small autochthonous additions during a broad summer peak. Temporal variability in DOC was low relative to macronutrients and chlorophyll in both reservoirs and streams, indicating DOC may be a sensitive and readily detected indicator of temporal change in these systems. In regression analyses, watershed features accounted for more than 60% of overall cross-system variability in DOC in both reservoirs and streams. Driver-response relations, however, differed between regions. This analysis extends our understanding of environmental influences on surface water chemistry in Missouri and indicates DOC is nearly as predictable as macronutrients using landscape-level features.

Floral scents, specialized metabolites and stress-response activities in Heritiera fomes and Bruguiera gymnorrhiza from Sundarban mangrove ecosystem.

Floral biochemistry and stress physiology is an underexplored aspect of mangroves, which should be investigated as part of preservation and restoration efforts. A thriving true mangrove tree (Bruguiera gymnorrhiza (L.) Lamk.) and a threatened mangrove-associate species (Heritiera fomes Buch. Ham.) were studied in the Sundarban region of India for seasonal variations in floral odours, non-volatile phytochemicals, antioxidant enzyme activities, and surface water chemistry in surrounding habitat. Both species were found to exhibit significant differences in floral volatilomes, protein contents, antioxidant enzyme activities, total flavonoids, and total phenolic contents between spring and autumn blooms. The bird-pollinated flowers of B. gymnorrhiza also showed considerable seasonal differences in floral anthocyanin and proline contents, indicating vulnerability of the post-anthesis open flowers to environmental factors. Contrarily to previous findings, B. gymnorrhiza floral bouquet appeared to be enriched in various classes of volatiles - dominated by sulphurous compounds in bud stage and terpenoids in open stage. Floral anthocyanins, contributing to the striking colouration of the calyx, were found to comprise cyanidin and delphinidin derivatives. Other glycosides of cyanidin and delphinidin were detected in H. fomes flowers, contributing to visual guides to potential food rewards for pollinating insects. Floral tissue in H. fomes was found to be protected by densely overlapping layers of stellate trichomes containing sesquiterpenoids as phytoprotectants. Comparison of the two floral species suggested that H. fomes flowering is optimized to oligohaline (but not freshwater) vernal conditions; whereas B. gymnorrhiza blooms are adapted for biologically enriched (including abundant herbivores and microbial growth), mesohaline forest habitats.

Reservoir Drawdown Highlights the Emergent Effects of Water Level Change on Reservoir Physics, Chemistry, and Biology

AbstractWater level drawdowns are increasingly common in lakes and reservoirs worldwide as a result of both climate change and water management. Drawdowns can have direct effects on physical properties of a waterbody (e.g., by altering stratification and light dynamics), which can interact to modify the waterbody's biology and chemistry. However, the ecosystem‐level effects of drawdown remain poorly characterized in small, thermally stratified reservoirs, which are common in many regions of the world. Here, we intensively monitored a small eutrophic reservoir for 2 years, including before, during, and after a month‐long drawdown that reduced total reservoir volume by 36%. During drawdown, stratification strength (maximum buoyancy frequency) and surface phosphate concentrations both increased, contributing to a substantial surface phytoplankton bloom. The peak in phytoplankton biomass was followed by cascading changes in surface water chemistry associated with bloom degradation, with sequential peaks in dissolved organic carbon, dissolved carbon dioxide, and ammonium concentrations that were up to an order of magnitude higher than the previous year. Dissolved oxygen concentrations substantially decreased in surface waters during drawdown (to 41% saturation), which was associated with increased total iron and manganese concentrations. Combined, our results illustrate how changes in water level can have cascading effects on coupled physical, chemical, and biological processes. As climate change and water management continue to increase the frequency of drawdowns in lakes worldwide, our results highlight the importance of characterizing how water level variability can alter complex in‐lake ecosystem processes, thereby affecting water quality.

Hydrochemical and Isotopic Characteristics and the Spatiotemporal Differences of Surface Water and Groundwater in the Qaidam Basin, China

In the context of climate change, precipitation and runoff in the arid inland basins of northwest China have undergone significant changes. The Qaidam Basin (QB) is a typical highland arid inland area. Understanding the spatial and temporal variations in surface water and groundwater chemistry and isotopes, as well as their causes, is crucial for future water resource management and ecological protection. Samples of river, lake, and groundwater, as well as others, were collected and tested in five typical watersheds in the summer and winter. The hydrochemistry and isotopic spatiotemporal differences in various water bodies were studied using the significant difference method, water vapor flux models, hydrochemistry, isotopes, and other methods for cause analyses. The results indicate the following: (1) There are differences in hydrochemistry between the southern and northern basins because the southern basin is more influenced by the dissolution of salt rocks and evaporation, whereas the northern basin is mainly affected by carbonate weathering. (2) The enrichment of δD and δ18O in the northern basin gradually increases from west to east, while in the southern basin, it is the opposite. This is because the southern basin receives a larger contribution of water vapor from the mid-latitude westerlies, while the northern basin primarily relies on local evaporation as its water vapor source. (3) Significant differences are observed in the total dissolved solids (TDS) and hydrochemical types of river water and groundwater between the summer and winter due to higher rates of rock weathering and evaporation in the summer. (4) The more pronounced seasonal differences in hydrogen and oxygen stable isotopes in the southern basin are due to higher rates of internal water vapor circulation in the summer. (5) The similarity in characteristics between river water and groundwater is the result of strong exchanges between river water and groundwater from piedmonts to terminals. The spatiotemporal heterogeneity of terminal lakes is attributed to the accumulation of salts and groundwater replenishment from other sources.

Heavy metal concentrations in surface waters of Hurghada and environs, Red Sea Coast, Egypt, and their correlation with sediment distribution

This study investigates the properties and chemistry of surface water in Hurghada and its adjacent areas, with a focus on assessing the potential impact of human activities on water quality by measuring the concentrations of heavy metals in surface water samples. A total of fifty-nine surface water samples were collected and analyzed for various heavy metals, including manganese (Mn), iron (Fe), nickel (Ni), copper (Cu), zinc (Zn), cadmium (Cd), mercury (Hg), and lead (Pb) using the AAS technique.The results indicate that at the Desert Rose Resort transect, the average total concentrations of heavy metals were within the following ranges: Fe (average of 26.96 μg/L), Cu (average of 0.61 μg/L), Zn (average of 6.31 μg/L), and Pb (average of 0.75 μg/L). Conversely, at the Abu-Shaar transect, Ni (0.87 μg/L) and Cd (average of 0.02 μg/L) were the dominant heavy metals, while Mn exhibited the highest mean value (1.80 μg/L) at the El-Samaka Village transect. Notably, Hg was not detected in any of the samples within the study areas.Comparative analysis of heavy metal concentrations in Hurghada's surface waters with data from the Red Sea coast and other global regions reveals that the study areas maintain heavy metal concentrations well below the maximum permissible values for the marine environment. These findings suggest that human activities have not significantly impacted heavy metal levels in the region's surface waters.Additionally, statistical assessments, such as correlation coefficients (r), were employed to explore the relationships between heavy metal concentrations in water and sediment. These relationships provide valuable insights into the dynamic balance of elements within the sediment and their potential direct or indirect transfer into the water.

Delayed recovery of surface water chemistry from acidification in subtropical forest region of China

The three largest acid rain regions of current earth are located in northern and western Europe, eastern North America, and East Asia. Sulfur and nitrate concentrations in headwater streams in Europe and North America decreased as atmospheric sulfur and nitrogen deposition decreased, albeit with a considerable delay. However, how water chemistry responds to the declining sulfur and nitrogen deposition in China is unclear. The regional survey of surface water chemistry during 2010 and 2018 within the Sichuan Basin in southwestern China showed that the recovery of the surface water chemistry was delayed for at least 5 years owing to the release of previously deposited sulfur and nitrogen stored in the soil. After sulfur deposition declined from its peak value, the subregions of purplish soil with low sulfate adsorption capacity still exhibited a net sulfur release in 2010, but this release was no longer evident by 2018. The subregions with the red and yellow soils, which have a high sulfate adsorption capacity, operated as sulfur sinks during 2010 and 2018, indicating a continuous immobilization process through sulfate reduction despite a decrease in sulfur deposition. Additionally, this sulfate reduction countered the release of sulfate caused by sulfur desorption. There was a substantial nitrogen sink within the Sichuan Basin. Nitrogen leaching decreased slowly with the declined nitrogen deposition, except in regions where nitrogen deposition exceeded the critical threshold. Compared to temperate forest regions in Europe, the Sichuan Basin and its surrounding areas have experienced higher decline rates in the leaching of sulfur and nitrogen, highlighting that the subtropical forest region undergoes a faster restoration of surface water chemistry.

Radium Isotopes as Tracers of Shelf‐Basin Exchange Processes in the Eastern Arctic Ocean

AbstractRadium isotopes, which are sourced from sediments, are useful tools for studying potential climate‐driven changes in the transfer of shelf‐derived elements to the open Arctic Ocean. Here we present observations of radium‐228 and radium‐226 from the Siberian Arctic, focusing on the shelf‐basin boundary north of the Laptev and East Siberian Seas. Water isotopes and nutrients are used to deconvolve the contributions from different water masses in the study region, and modeled currents and water parcel back‐trajectories provide insights on water pathways and residence times. High radium levels and fractions of meteoric water, along with modeled water parcel back‐trajectories, indicate that shelf‐ and river‐influenced water left the East Siberian Shelf around 170°E in 2021; this is likely where the Transpolar Drift was entering the central Arctic. A transect extending from the East Siberian Slope into the basin is used to estimate a radium‐228 flux of 2.67 × 107 atoms m−2 d−1 (possible range of 1.23 × 107–1.04 × 108 atoms m−2 d−1) from slope sediments, which is comparable to slope fluxes in other regions of the world. A box model is used to determine that the flux of radium‐228 from the Laptev and East Siberian Shelves is 9.03 × 107 atoms m−2 d−1 (possible range of 3.87 × 107–1.56 × 108 atoms m−2 d−1), similar to previously estimated fluxes from the Chukchi Shelf. These three shelves contribute a disproportionately high amount of radium to the Arctic, highlighting their importance in regulating the chemistry of Arctic surface waters.

Heavy Metal Contamination Assessment in Sediments, Soils and Surface Waters in Agriculture-Based Rural Chhattisgarh, India, and Evaluation of Irrigation Water Quality

Regional geochemical mapping was carried out in Bilaspur and Korba Districts of Chhattisgarh, and stream sediments/slope wash, soil, and water samples were analyzed for concentration of heavy metals. The study contributes to understanding heavy metals contamination of sediments, soils, and water due to anthropogenic activity, mainly in agriculture-based rural areas. The study reveals that high geochemical anomalies observed for heavy metals like Ni, Cr, As, and Zn in sediments and soil samples are due to the extensive uses of phosphatic fertilizer and soil amendments in the form of poultry and swine manure. Water quality assessment of major streams in the study areas shows that the water is suitable for domestic and agricultural uses. Correlation analysis reveals that the chemical weathering of rock-forming minerals doesn’t control the surface water chemistry of the study area and is also an anthropogenic source of sodium in water. This study also shows the importance of the country’s geochemical mapping database, which will have much broader applications than conventional mineral exploration and geological mapping.

Hydrochemical and Stable Isotope characteristics of surface water and groundwater in Xiliugou and Wulagai River basin, North China

The investigation of the correlation between groundwater and surface water in terms of water origin and transformation is crucial for comprehending hydrological processes . Focuses on the Wulagai river and Xiliugou river basin located in East and West Inner Mongolia. It employs hydrochemical analysis and stable HO isotopes techniques to investigate the hydrochemical properties of the basin and quantitatively assess the interconversion between groundwater and surface water. The results suggest that the Xiliugou and Wulagai river basins were originally nourished by atmospheric precipitation, with lower δD and δ18O values in groundwater compared to surface water, attributed to factors such as evaporation, water vapor source, altitude, and latitude. The surface waters in the Xiliugou and Wulagai River exhibit dominance of Na•Ca-SO4•HCO3 and Ca•Na-HCO3 types, respectively, while the groundwater is characterized by dominance of Na•Ca-HCO3 and Ca•Mg-HCO3 types, respectively. The water chemistry of surface water and groundwater in the two basins is influenced by water-rock interactions and processes of evaporation and concentration, primarily observed in the dissolution of carbonate rocks and evaporites. Hydrograph separation using End-Members Mixing Analysis (EMMA) revealed that during the growing season, groundwater in Xiliugou was primarily recharged by precipitation (76.87 %) and surface water (23.13 %), while in Wulagai, groundwater was mainly recharged by precipitation (65 %) and surface water (35 %). The presence of comparable hydrochemical constituents and shared regulatory mechanisms between groundwater and surface water within a given basin provides further evidence of a discernible hydraulic interconnection, primarily driven by the replenishment of groundwater through surface water recharge.

Hydrochemical Characteristics and Control Factors of Surface Water in Kuaize River Basin at the Upper Pearl River

The Kuaize River is a small typical karst watershed in the source area of the Pearl River as well as an important coal mining area in Eastern Yunnan with a fragile ecological environment. Strengthening the research on the water environment in the region plays an important role in supporting the comprehensive management of the ecological environment and water resources in the source region of the Pearl River. Through the systematic collection of surface water, karst groundwater, and mine water samples, mathematical statistics analysis, correlation analysis, ion ratio analysis, absolute principal component scores multiple linear regression(APCS-MLR), and other methods were used to study the characteristics of hydrochemical evolution and control factors in Kuaize River Basin. The results showed that the average pH value of surface water in Kuaize River Basin was 7.8, which was weakly alkaline. The main cations were Ca2+ and Na+, showing the characteristics of Ca2+>Na+>Mg2+>K+. The main anions were HCO3- and SO42-, showing the characteristics of HCO3->SO42->NO3->Cl-. The variation coefficients of Na+, SO42-, and NO3- in surface water were high, showing strong spatial variability. The water chemical type of the trunk stream was mainly HCO3-Ca, whereas the water chemical type of the tributary was relatively complex, mainly HCO3-Ca, HCO3-Ca·Na, and HCO3·SO4-Ca·Na. The chemical composition of surface water was mainly affected by rock weathering, cation exchange, and human activities. Ca2+, Mg2+, Na+, and HCO3- in surface water mainly came from the weathering of carbonate rock and silicate rock; SO42- mainly came from the oxidation of sulfide, such as pyrite in coal seams; K+, Cl-, and NO3- mainly came from domestic sewage and agricultural activities. The APCS-MLR receptor model analysis results showed that the surface water in the Kuaize River Basin was mainly affected by sulfide oxidation, carbonate weathering, weathering of silicate rock in mine water, domestic sewage, agricultural activities, and unknown sources. In general, the contribution rate of human activities such as mining, domestic sewage, and agricultural activities to the surface water reached 47.17%, indicating that human activities were the key driving factor of surface water chemistry in the Kuaize River Basin.

The recovery of crustacean zooplankton from acidification depends on lake type.

Acidification has harmed freshwater ecosystems in Northern Europe since the early 1900s. Stricter regulations aimed at decreasing acidic emissions have improved surface-water chemistry since the late 1980s but the recovery of biotic communities has not been consistent. Generally, the recovery of flora and fauna has been documented only for a few lakes or regions and large-scale assessments of long-term dynamics of biotic communities due to improved water quality are still lacking. This study investigates a large biomonitoring dataset of pelagic and littoral crustacean zooplankton (Cladocera and Copepoda) from 142 acid-sensitive lakes in Norway spanning 24 years (1997-2020). The aims were to assess the changes in zooplankton communities through time, compare patterns of changes across lake types (defined based on calcium and humic content), and identify correlations between abiotic and biological variables. Our results indicate chemical and biological recovery after acidification, as shown by a general increase in pH, acid neutralizing capacity, changes in community composition and increases in the total number of species, number of acid-sensitive species and functional richness through time. However, the zooplankton responses differ across lake types. This indicates that the concentration of calcium (or alkalinity) and total organic carbon (or humic substances) are important factors for the recovery. Therefore, assessment methods and management tools should be adapted to the diverse lake types. Long-term monitoring of freshwater ecosystems is needed to fully comprehend the recovery dynamics of biotic communities from acidification.

A probabilistic assessment of surface water-groundwater exchange flux at a PCE contaminated site using groundwater modelling

Polluted groundwater discharge at a chlorinated solvent contaminated site in Hagfors, Sweden, is affecting a nearby stream flowing through a sparsely populated area. Because of difficulties related to source zone remediation, decision makers recently changed the short-term site management objective to mitigating discharge of polluted groundwater to the stream. To help formulating targeted remediation strategies pertaining to the new objective, we developed a groundwater numerical decision-support model. To facilitate reproducibility, the modelling workflow was scripted. The model was designed to quantify and reduce the uncertainty of surface water-groundwater (SW-GW) exchange fluxes for the studied period (2016–2020) through the use of history-matching. In addition to classical observations, thermal anomalies detected in fiber optic distributed temperature sensing (FO-DTS) measurements were used to inform the model of groundwater discharge. After assessing SW-GW exchange fluxes, we used measurements of surface water chemistry to provide a probabilistic estimation of mass influx and spatio-temporal distributions of contaminated groundwater discharge. Results show 1) SW-GW exchange fluxes are likely to be significantly larger than previously estimated, and 2) prior estimations of mass influx are located near the center of the posterior probability distribution. Based on this, we recommend decision makers to focus remediation action on specific segments of the stream.