Water Chemistry Research Articles

Using Geochemical Tracers to Determine Seasonal Inputs of Freshwater to a Coastal Estuary: Biscayne Bay, FL

Biscayne Bay is a coastal estuary that historically relied on rainfall and groundwater inputs from the karst Biscayne aquifer. The construction of major canals along the coastline has released point-source freshwater inputs into the bay, detrimentally affecting the Bay’s ecosystem balance. This project investigates the proportional inputs of freshwater between the wet and dry seasons in Deering Estate, adjacent to Biscayne Bay. The objective of this project was accomplished by analyzing the water chemistry of the bay using naturally occurring geochemical tracers. Water sampling occurred from May to August (wet season 2022) and January to March (dry season 2023); at an inland freshwater spring and on Biscayne Bay. Water samples were analyzed for δ18O and δ2H values, and Sr2+/Ca2+ ratios as geochemical tracers. The highest and lowest salinity values observed in the wet and dry seasons, at both the freshwater spring and Biscayne Bay sites, were before and after a major rain event, respectively. The chemical analysis supports that rain is the dominant source of freshwater input into the bay at our sampling location, and the freshwater spring is dominated by groundwater and canal water during the wet season. During the dry season, groundwater and canal water are the dominant source for the sampling location in Biscayne Bay and the dominant source of freshwater input for the freshwater spring. However, all three endmembers contribute seasonally. Understanding freshwater inputs to this crucial estuary will provide important information for current restoration efforts of Biscayne Bay, specifically around the Deering Estate area.

Diffusion in Porous Rock Is Anomalous.

Molecular diffusion of chemical species in subsurface environments─rock formations, soil sediments, marine, river, and lake sediments─plays a critical role in a variety of dynamic processes, many of which affect water chemistry. We investigate and demonstrate the occurrence of anomalous (non-Fickian) diffusion behavior, distinct from classically assumed Fickian diffusion. We measured molecular diffusion through a series of five chalk and dolomite rock samples over a period of about two months. We demonstrate that in all cases, diffusion behavior is significantly different than Fickian. We then analyze the results using a continuous time random walk framework that can describe anomalous diffusion in heterogeneous porous materials such as rock. This methodology shows extreme long-time tailing of tracer advance as compared to conventional Fickian diffusion processes. The finding that distinct anomalous diffusion occurs ubiquitously implies that diffusion-driven processes in subsurface zones should be analyzed using tools that account for non-Fickian diffusion.

GEOLOGY AND THE STUDY OF HEAVY METAL IMPACTS ON ENVIRONMENTAL QUALITY ASSESSMENT USING ARCGIS FOR INTERPRETATION DISTRIBUTION

The Boto area, Jatiroto District, Wonogiri Regency, Central Java, Indonesia, is a traditional gold mining site with inadequate waste management practices, particularly mercury usage. This study aims to assess mercury contamination and evaluate phytoremediation potential in the area. Geological mapping, petrographic analysis, fossil analysis, stereographic analysis, soil Hg measurement, soil and water chemistry analysis, and XRF analysis were conducted to characterize the geology, geomorphology, and heavy metal distribution. The study area is divided into four geomorphological units: Intrusive Hill Unit (V1), Homoklin Hill Unit (S1), Karst Hill Unit (K1), and Alluvial Plain Unit (F1). Stratigraphically, the area consists of the Nglanggeran Breccia Unit interbedded with early Miocene lava, the early Miocene andesite Intrusion Unit with a terrestrial depositional environment, the Wonosari Limestone Unit of Middle-Late Miocene age, and the Holocene Alluvial Deposit Unit. Geological structures include left-lateral normal faults trending relatively north-south (Sesar Boto), left-lateral normal faults trending southeast-northwest (Sesar Brenggolo), and right-lateral downthrown faults trending southeast-northwest (Sesar Mesu). Fractures and veins are also present. Mercury (Hg), manganese (Mn), arsenic (As), and lead (Pb) distribution mapping was conducted. The contaminated zone falls into TCLP-A, and waste management falls into category 1, located in Boto Village, which is a gold mining and processing area. Phytoremediation is proposed as a remediation strategy. Keywords: gold mining, heavy metals, XRF, phytoremediation, distribution

Integrating depth-dependent protist dynamics and microbial interactions in spring succession of a freshwater reservoir

BackgroundProtists are essential contributors to eukaryotic diversity and exert profound influence on carbon fluxes and energy transfer in freshwaters. Despite their significance, there is a notable gap in research on protistan dynamics, particularly in the deeper strata of temperate lakes. This study aimed to address this gap by integrating protists into the well-described spring dynamics of Římov reservoir, Czech Republic. Over a 2-month period covering transition from mixing to established stratification, we collected water samples from three reservoir depths (0.5, 10 and 30 m) with a frequency of up to three times per week. Microbial eukaryotic and prokaryotic communities were analysed using SSU rRNA gene amplicon sequencing and dominant protistan groups were enumerated by Catalysed Reporter Deposition-Fluorescence in situ Hybridization (CARD-FISH). Additionally, we collected samples for water chemistry, phyto- and zooplankton composition analyses.ResultsFollowing the rapid changes in environmental and biotic parameters during spring, protistan and bacterial communities displayed swift transitions from a homogeneous community to distinct strata-specific communities. A prevalence of auto- and mixotrophic protists dominated by cryptophytes was associated with spring algal bloom-specialized bacteria in the epilimnion. In contrast, the meta- and hypolimnion showcased a development of a protist community dominated by putative parasitic Perkinsozoa, detritus or particle-associated ciliates, cercozoans, telonemids and excavate protists (Kinetoplastida), co-occurring with bacteria associated with lake snow.ConclusionsOur high-resolution sampling matching the typical doubling time of microbes along with the combined microscopic and molecular approach and inclusion of all main components of the microbial food web allowed us to unveil depth-specific populations’ successions and interactions in a deep lentic ecosystem.

Integrating geoelectrical and water chemistry studies to explore environmental challenges with an Indigenous community in northern Canada

Integrating geoelectrical and water chemistry studies to explore environmental challenges with an Indigenous community in northern Canada

Reservoir temperature prediction based on characterization of water chemistry data—case study of western Anatolia, Turkey

Reservoir temperature estimation is crucial for geothermal studies, but traditional methods are complex and uncertain. To address this, we collected 83 sets of water chemistry and reservoir temperature data and applied four machine learning algorithms. These models considered various input factors and underwent data preprocessing steps like null value imputation, normalization, and Pearson coefficient calculation. Cross-validation addressed data volume issues, and performance metrics were used for model evaluation. The results revealed that our machine learning models outperformed traditional fluid geothermometers. All machine learning models surpassed traditional methods. The XGBoost model, based on the F-3 combination, demonstrated the best prediction accuracy with an R2 of 0.9732, while the Bayesian ridge regression model using the F-4 combination had the lowest performance with an R2 of 0.8302. This study highlights the potential of machine learning for accurate reservoir temperature prediction, offering geothermal professionals a reliable tool for model selection and advancing our understanding of geothermal resources.

Assessing the efficacy of magnetic water treatment: A concise review and experimental investigation

The utilization of magnetic water treatment has gained significant attention as a promising method for addressing scaling and water quality issues. This strategy has attracted interest due to its ability to potentially alter the behavior of dissolved particles in water. This investigation aimed to examine the impact of magnetic water treatment utilizing two different pipe materials, "iron pipe" and "PVC pipe", with a specific emphasis on the levels of total dissolved salts (TDS). Unexpectedly, the research findings indicate a positive correlation between the number of coil turns and the levels of TDS, which contradicts the popular belief that magnetic treatment would lead to a decrease in TDS. For instance, at a flow rate of 1mL/s, TDS levels increase from an average of 265 ppm to roughly 277 ppm utilizing 500 and 2000 coil turns around an iron pipe, respectively. Similarly, when using a PVC pipe, TDS levels increase from around 263 ppm to 271 ppm as the magnetic field intensity increases. Furthermore, experiments carried out at an increased flow rate under a constant magnetic field strength show an inverse relationship with TDS. The TDS levels fall from 265 ppm to 261 ppm and from 263 ppm to 260 ppm as the flow rate rises from 1mL/s to 6mL/s for iron and PVC pipes, respectively. This intriguing phenomenon presents a challenge to long-held theories and highlights the complex relationship between magnetic fields, pipe materials, and water chemistry. Despite the unexpected results, the increase in the total dissolved salts indicates a possible improvement in reducing scaling, a common problem in fluid systems. In this discourse, this study analyzes the ramifications of these discoveries and underscores the necessity for additional investigation in order to elucidate the intricate mechanisms that underlie these interactions and enhance the efficacy of magnetic water treatment approaches. This research enhances the comprehension of water treatment strategies and emphasizes the significance of customizing procedures to suit individual scenarios in order to achieve efficient water quality control.

Acid mine drainage from coal mines in the eastern Himalayan sub-region: Hydrogeochemical processes, seasonal variations and insights from hydrogen and oxygen stable isotopes

Uncontrolled coal mining using non-scientific methods has presented a major threat to the quality of environment, particularly the water resources in eastern himalayan sub-region of India. Water bodies in the vicinity of mining areas are contaminated by acid mine drainage (AMD) that is released into streams and rivers. This study attempted to assess the impact of AMD, deciphering hydrogeochemical processes, seasonal fluctuations, and stable isotope features of water bodies flowing through and around coal mining areas. Self-organising maps (SOMs) used to separate and categorize AMD, AMD-impacted and non-AMD impacted water from the different study locations for two sampling seasons revealed four clusters (C), with C1 and C2 impacted by AMD, C3 and C4 showing negligible to no impact of AMD. AMD impacted water was SO42- - Mg2+- Ca2+ hydrochemical type with sulphide oxidation and evaporation dominating water chemistry, followed by silicate weathering during both the sampling seasons. Water with negligible-to-no AMD-impact was Mg2+- Ca2+- SO42- to Ca2+ - HCO3- to mixed hydrochemical type with rock weathering and dissolution, followed by ion exchange as major factors controlling water chemistry during both the sampling seasons. Most of physicochemical parameters of C1 and C2 exceeded the prescribed limits, whereas in C3 and C4 water samples, parameters were found within the prescribed limits. Stable isotopes of hydrogen (δ2H) and oxygen (δ18O) during post-monsoon (PoM) varied between -29.98 ‰ to -41.04 ‰ and -6.60 ‰ to -3.94 ‰; and during pre-monsoon (PrM) varied between -58.18 ‰ to - 33.76 ‰ and -8.60 ‰ to -5.46 ‰. Deuterium excess (d-excess) ranged between 12.47 ‰ to 1.57 ‰ during PoM and 15.17 ‰ to 5.70 ‰ during PrM season. The stable isotopes analysis revealed that evaporation, mineral dissolution and mixing with rainwater are the key factors in study area.

Probe into Water Chemistry Effects on Internal Corrosion Risk for Sour Gas Pipelines

Probe into Water Chemistry Effects on Internal Corrosion Risk for Sour Gas Pipelines

Nb speciation and microstructural characterization of the oxide layer formed on neutron-irradiated Zr-2.5 Nb alloy in high-temperature water

It is crucial to understand the degradation mechanisms of the alloy Zr-2.5Nb, which make the pressure boundary in Canada Deuterium Uranium reactors. In the present study, Zr-2.5Nb coupons were exposed for 567 days at 325 °C with and without neutron-irradiation in simulated primary water chemistry. A combination of scanning/transmission electron microscopy with energy dispersive X-ray spectroscopy, and electron energy loss spectroscopy was used to investigate the base metal and oxide. The obtained results suggest that the distribution of nanopores and the variation in Nb oxidation state likely create a gradient in the oxygen concentration and electrochemical potential through the film.

Influence of clay minerals on pH and major cation concentrations in acid-leached sands: Column experiments and reactive-transport modeling

A series of laboratory experiments are conducted to simulate the acidification and subsequent recovery of a sand aquifer exploited by in situ recovery (ISR) mining. A sulfuric acid solution (pH 2) is first injected into a column packed with sand from the Zoovch Ovoo uranium roll front deposit (Mongolia). Solutions representative of local groundwater or enriched in cations (Na+, Mg2+) are then circulated through the column to simulate the inflow of aquifer water. pH and major ion concentrations (Na+, Cl−, SO42−, Ca2+, Mg2+, K+) measured at the column outlet reproduce the overall evolution of porewater chemistry observed in the field. The presence of minor quantities of swelling clay minerals (≈6 wt% smectite) is shown to exert an important influence on the behavior of inorganic cations, particularly H+, via ion-exchange reactions. Numerical models that consider ion-exchange on smectite as the sole solid-solution interaction are able to reproduce variations in pH and cation concentrations in the column experiments. This highlights the importance of clay minerals in controlling H+ mobility and demonstrates that sand from the studied aquifer can be described to a first order as an ion-exchanger. The present study confirms the key role of clay minerals in controlling water chemistry in acidic environments through ion-exchange processes. In a context of managing the long-term environmental footprint of industrial and mining activities (ISR, acid mine drainage…), this work will bring insights for modeling choices and identification of key parameters to help operators to define their production and/or remediation strategies.

High-resolution mapping and multivariate technique (factor analysis) to support hydrogeochemical analysis and identification of surface water contamination

The study presented a high-resolution regional mapping of a significant Brazilian watershed, which is heavily influenced by mining, agriculture, and domestic/industrial effluents. Upper São Francisco Basin encompasses the largest karst area in the country and includes three important Brazilian biomes: Cerrado, Atlantic Forest, and Caatinga. Surface water (1418 samples) was collected during the dry season and was analyzed for physical-chemical parameters, cations, anions, and some metals. The spatial distribution and abundance of variables were assessed, and the processes controlling the sources of dissolved loads in surface waters were discussed. The results indicate that rock weathering is the primary factor controlling water chemistry, with a strong influence of carbonate and silicate minerals. Anthropogenic activities, particularly agriculture, play a key role in the chemical composition of the microbasins. Soil erosion and leaching processes also contribute significantly to the region, driven by land use practices and mineral extraction, which intensify erosion processes. The northern sector of the Upper São Francisco Basin, characterized by an arid climate and Caatinga vegetation, experiences low precipitation and high evapotranspiration rates. The VG stands out due to the presence of the karst zone and for the mixture of natural to anthropogenic sources.

Ведение ВХР с применением реагентов ВТИАМИН на ТЭЦ с сезонным режимом работы

The main equipment of the thermal power plant (TPP) includes a E-120-7.0-500GM steam boiler produced by LLC “Belenergomash – BZEM” with a single-stage evaporation circuit. The operating mode of the thermal power plant has seasonal characteristics. During the period of February to the end of August the equipment is stopped as a reserve. Dosing of AMINAT PK-3 does not provide the required pH level in steam and feed water, so the reagent for water-chemical regime and preservation has been substituted with VTIAMIN KR-33. The complex reagent VTIAMIN KR-33 ensures both the maintenance of the required quality indicators of the coolant along the path and promotes the formation of a protective barrier film on the internal heating surfaces. To check water-chemical regime, the existing automatic chemical control system has been updated. Panels have been installed for automatic chemical control of pH value, electrical conductivity of direct and H-cationized samples. The filter material has been replaced and the mechanical filters have been connected. The first stage of the filter has been replaced, the second stage of the filter and final purification filters Н-OH have been installed. The authors have demonstrated the possibility to use boilers with seasonal operating modes and measuring the electrical conductivity of cooled water and steam samples as a chemical control of water chemistry. It is found out that dosing the VTIAMIN KR-33 reagent with periodic dosing of the VTIAMIN D-8 reagent into the boiler water prevent the precipitation of hardness salts and other impurities coming with the return condensate. Analysis of the indicators of the water chemistry regime at the thermal power plant when dosing the VTIAMIN KR-33 reagent at two points has shown that the pH value of the feed water is in the range of 8,8–9,0 and the indicators of the water chemistry regime in terms of the content of iron, silicic acid and sodium are also within the norm limits. The composition of the reagents is selected. Flexibility of water chemistry management is ensured. It has been shown that the dosage of the amine-containing reagent VTIAMIN neutralizes the negative effects of aggressive gases (carbon dioxide and oxygen) due to their binding and the formation of a protective film of the magnetite-amine type on heating surfaces. Introduction of the water chemical regime when the equipment is stopped as a reserve does not require additional preservation measures.

Volcanic Glass as a Proxy for Paleotopography Suggests New Features in Late-Miocene Oregon

Volcanic glass has been used extensively as a paleoaltimeter. Deuterium (2H) concentrations in glass have been found to be stable over geologic timescales, making δ2H (also known as δD) a reliable proxy for ancient water chemistry. However, continued work revolves around better understanding how different factors affect preserved water in volcanic ash. Here, we analyze δD in the Rattlesnake Tuff (RST), a widespread ca. 7 Ma ash-flow tuff, and create a paleoisoscape to assess variations in δD across Oregon during that time. To this end, 16 ash samples were collected across central and eastern Oregon from various flow units within the RST. Samples were analyzed for δD using a temperature conversion elemental analyzer (TC/EA) connected to a mass spectrometer and elemental composition using a scanning electron microscope (SEM). We compared the isotopic results to modern water and published ancient water proxy data to better constrain changes in climate and topography across Oregon throughout the Neogene. We also estimated wt. % H2O by calculating excess (non-stoichiometric) oxygen from SEM elemental data. We did not observe significant variations in δD among the flow units from single locations, nor was there a significant relationship between the prepared glass shard composition and wt. % H2O or δD, supporting the use of volcanic glass as a reliable paleoenvironmental indicator. Our results show significant spatial variation in δDwater values of RST, ranging from −107‰ to −154‰. δD values of ancient glass were similar to modern water near the Cascade Mountains but became relatively negative to the east near the inferred eruptive center of the RST, suggesting that a significant topographic feature existed in the vicinity of the RST eruptive center that has since subsided.

Porewater microbiomes in buried wetland soils: Synergic effects of water chemistry and redox gradients associated with hydrological processes

Abstract Interstitial water or pore water occupies the space between soil particles and provides “hotspots” and “fluvial networks” for microbial activities in floodplain soil. However, to date, we know very little about the microorganisms living in pore water and how they respond to environmental changes. This study aimed to understand microbial distribution and assemblage in riparian pore waters, and how they respond to water chemistry and redox gradients associated with hydrological processes. We analysed the annual changes of porewater microbial communities from the east and west banks of the White Clay Creek, a site at the Christina River Basin – Critical Zone Observatory, Pennsylvania, USA. Microbial abundances were quantified by epifluorescence microscopy and detailed community structures were characterised by high‐throughput sequencing. Water chemistry and redox gradients were also monitored and recorded, and their interactions with porewater microbiomes were analysed using correlations and multivariate analyses. Abundance of microbial cells increased during summer and late autumn. Wetland porewater microbiomes mainly contained Acidobacteria, Bacteroidetes, Nitrospirae and Proteobacteria, and microbiome structures were easily distinguishable from those in the underlying hyporheic gravel layer. Seasonal dynamics of bacterial community structure in the east and west wetlands were distinct, responding to floodplain topography and associated hydrological/geochemical processes. Iron (Fe)‐cycling bacteria (mainly Gallionellaceae and Rhodoferax spp.) dominated the porewater microbiome, and their relative abundance was significantly higher in the east than the west wetland. Furthermore, Fe‐oxidising bacteria (Gallionellaceae) were negatively correlated with Fe‐reducing bacteria (Rhodoferax spp.) at the east wetland. Microbial abundances (cell density) in pore waters showed similar seasonal patterns across stream banks, but microbial community structure did not. Microbiome assembly in pore water is correlated with water chemistry and redox gradients primarily associated with local hydrological processes. As a consequence of their significance for carbon (C) mineralisation and Fe reduction at terrestrial–aquatic interfaces, microbiomes in riparian pore waters and associated microbial activity play an essential role in C and mineral dynamics. These findings will inform future studies of the response of freshwater ecosystems to hydrological dynamics influenced by global climate change.

Use of Unmanned Surface Vehicles (USVs) in Water Chemistry Studies.

Unmanned surface vehicles (USVs) equipped with integrated sensors are a tool valuable to several monitoring strategies, offering enhanced temporal and spatial coverage over specific timeframes, allowing for targeted examination of sites or events of interest. The elaboration of environmental monitoring programs has relied so far on periodic spot sampling at specific locations, followed by laboratory analysis, aiming at the evaluation of water quality at a catchment scale. For this purpose, automatic telemetric stations for specific parameters have been installed by the Institute of Marine Biological Resources and Inland Waters of Hellenic Centre for Marine Research (IMBRIW-HCMR) within several Greek rivers and lakes, providing continuous and temporal monitoring possibilities. In the present work, USVs were deployed by the Athens Water and Sewerage Company (EYDAP) as a cost-effective tool for the environmental monitoring of surface water bodies of interest, with emphasis on the spatial fluctuations of chlorophyll α, electrical conductivity, dissolved oxygen and pH, observed in Koumoundourou Lake and the rivers Acheloos, Asopos and Kifissos. The effectiveness of an innovative heavy metal (HM) system installed in the USV for the in situ measurements of copper and lead was also evaluated herewith. The results obtained demonstrate the advantages of USVs, setting the base for their application in real-time monitoring of chemical parameters including metals. Simultaneously, the requirements for accuracy and sensitivity improvement of HM sensors were noted, in order to permit full exploitation of USVs' capacities.

New Insights into Aggregation Behaviors of the UV-Irradiated Dissolved Biochars (DBioCs) in Aqueous Environments: Effects of Water Chemistries and Variation in the Hamaker Constant.

The aggregation behavior of ubiquitous dissolved black carbon (DBC) largely affects the fate and transport of its own contaminants and the attached contaminants. However, the photoaging processes and resulting effects on its colloidal stability remain yet unknown. Herein, dissolved biochars (DBioCs) were extracted from common wheat straw biochar as a proxy for an anthropogenic DBC. The influences of UV radiation on their aggregation kinetics were systematically investigated under various water chemistries (pH, electrolytes, and protein). The environmental stability of the DBioCs before and after radiation was further verified in two natural water samples. Hamaker constants of pristine and photoaged DBioCs were derived according to Derjaguin-Landau-Verwey-Overbeek (DLVO) prediction, and its attenuation (3.19 ± 0.15 × 10-21 J to 1.55 ± 0.07 × 10-21 J after 7 days of radiation) was described with decay kinetic models. Pearson correlation analysis revealed that the surface properties and aggregation behaviors of DBioCs were significantly correlated with radiation time (p < 0.05), indicating its profound effects. Based on characterization and experimental results, we proposed a three-stage mechanism (contended by photodecarboxylation, photo-oxidation, and mineral exposure) that DBioCs might experience under UV radiation. These findings would provide an important reference for potential phototransformation processes and relevant behavioral changes that DBC may encounter.

The influence of atmospheric deposition and climate change driven catchment internal processes on the recovery from acidification of high-altitude Alpine lakes

The impact of atmospheric deposition and environmental factors on catchment processes and water chemistry of 20 high-altitude Alpine lakes in Southern Switzerland was investigated over four decades. Through the analysis of input-output budgets of sulphur (S), nitrogen (N), base cations and alkalinity significant trends emerged. Notably, S and N input concentrations significantly declined since the 1980s, by approximately 78 % and 22 %, respectively, with N primarily declining after 2000. Recovery from acidification was slightly delayed, likely due to the increased release of S, possibly originating from legacy S pools, alongside the simultaneous reduction in leaching of base cations from exchange sites. Catchments heavily impacted by thawing cryospheric features increasingly released S and base cations due to enhanced weathering processes, with hardly any impact on the recovery process, as evidenced by the balanced releases of S and base cations. N output concentrations followed the decrease of N input concentrations, while the relative N retention in the catchments remained relatively stable. Recently, both input concentrations of S and N have stabilised, while output concentrations of base cations began to increase across all catchments. The trend likely arises from the stabilisation of S and N input concentrations and/or the ongoing increase in weathering rates induced by climate change. Consequently, there was a consistent rise in alkalinity output concentrations even after the stabilisation of the S and N input concentrations. Ion ratio analysis suggests that carbonation primarily drives weathering processes in catchment areas unaffected by thawing cryosphere, while in areas impacted by thawing cryosphere, sulphide oxidation (or sulphate dissolution) is the dominant process. Further recovery depends on future N deposition and the effects of climate change.

The Hydrogeochemistry of and Earthquake-Related Chemical Variations in the Springs along the Eastern Kunlun Fault Zone, China

The Eastern Kunlun Fault (EKF) is situated in an area with a history of significant seismic events, yet it has witnessed a dearth of major earthquakes in recent years. This study conducted a detailed analysis of the hydrogeochemical characteristics of the springs in the EKF and their temporal variation, aiming to address the gaps in the research on the hydrogeochemistry in the region and to investigate the changes in water chemistry during the seismogenic process. In this study, the main elements, trace elements, hydrogen isotopes, oxygen isotopes, and strontium isotopes of 23 springs in the EKF were analyzed. The results indicated that the groundwater recharge in the eastern part of the Eastern Kunlun Fault Zone mainly originates from atmospheric precipitation, as supported by its isotopic characteristics. The spring water is immature, showing weak water–rock interactions. A hydrochemical analysis classified the springs into 11 main types, reflecting varying degrees of water–rock interaction. Based on measurements using quartz geothermometers, the estimated geothermal reservoir temperatures ranged from 39.6 to 120.3 °C, with circulation depths of 1.3 to 3.8 km. By means of regularly monitoring three selected springs, this study also explored the relationship between earthquakes and hot spring chemical variations. Finally, a conceptual model of hydrogeochemistry was proposed to describe the groundwater circulation in the study area.

Low adsorption affinity of athabasca oil sands naphthenic acid fraction compounds to a peat-mineral mixture

Much of the toxicity in oil sands process-affected water in Athabasca oil sands tailings has been attributed to naphthenic acids (NAs) and associated naphthenic acid fraction compounds (NAFCs). Previous work has characterized the environmental behaviour and fate of these compounds, particularly in the context of constructed treatment wetlands. There is evidence that wetlands can attenuate NAFCs in natural and engineered contexts, but relative contributions of chemical, biotic, and physical adsorption with sequestration require deconvolution. In this work, the objective was to evaluate the extent to which prospective wetland substrate material may adsorb NAFCs using a peat-mineral mix (PMM) sourced from the Athabasca Oil Sands Region (AOSR). The PMM and NAFCs were first mixed and then equilibrated across a range of NAFC concentrations (5–500 mg/L) with moderate ionic strength and hardness (∼200 ppm combined Ca2+ and Mg2+) that approximate wetland water chemistry. Under these experimental conditions, low sorption of NAFCs to PMM was observed, where sorbed concentrations of NAFCs were approximately zero mg/kg at equilibrium. When NAFCs and PMM were mixed and equilibrated together at environmentally relevant concentrations, formula diversity increased more than could be explained by combining constituent spectra. The TOC present in this PMM was largely cellulose-derived, with low levels of thermally recalcitrant carbon (e.g., lignin, black carbon). The apparent enhancement of the concentration and diversity of components in PMM/NAFCs mixtures are likely related to aqueous solubility of some PMM-derived organic materials, as post-hoc combination of dissolved components from PMM and NAFCs cannot replicate enhanced complexity observed when the two components are agitated and equilibrated together.