Origin and Circulation of Springs in the Nangqen and Qamdo Basins, Southwestern China, Based on Hydrochemistry and Environmental Isotopes

The Nangqen and Qamdo (NQ-QD) basins in China have very rich geothermal and brine resources. The origin and spatiotemporal evolutionary processes of its hot and saline springs however remain unclear. Geochemical and isotopic (18O, 2H, 3H) studies have therefore been conducted on the water from the geothermal and saline springs in the NQ-QD Basin. All saline springs in the study area are of the Na-Cl geochemical type while geothermal waters show different geochemical types. The oxygen and hydrogen isotopic compositions of the springs in the NQ-QD Basin are primarily controlled by meteoric water or ice-snow melt water and are influenced by rock-water interactions. It is found that the saline springs in the study area are derived from the dissolution of halite and sulfate that occur in the tertiary Gongjue red bed, while the hot springs in the QD Basin are greatly influenced by the dissolution of carbonatites and sulfates from the Bolila (T3b) and Huakaizuo (J2h) formations. Results from silica geothermometry and a silicon-enthalpy hybrid model indicate that the apparent reservoir temperatures and reservoir temperatures for the hot springs in the QD Basin range from 57–130°C to75–214°C, respectively. Deuterium analysis indicates that most of the hot springs are recently recharged rain water. Furthermore, the saline springs have a weaker groundwater regeneration capacity than the hot springs. Tritium data shows that the ranges of calculated residence times for springs in this study are 25 to 55 years, and that there is a likelihood that hot springs in the QD Basin originated from two different hydrothermal systems. The geochemical characteristics of the NQ-QD springs are similar to those of the Lanping-Simao Basin, indicating similar solute sources. Thus, the use of water isotope analyses coupled with hydrogeochemistry proves to be an effective tool to determine the origin and spatiotemporal evolution of the NQ-QD spring waters.

Geochemical Techniques to Detect Sources of Fluids in Highly Pressured Casing-Casing Annuli CCA

The buildup of high casing-casing annulus (CCA) pressure compromises the well integrity and can lead to serious incidents if left untreated. Potential sources of water causing the elevated CCA pressure are either trapped water in the cement column or water from a constant feeding source. This study utilizes inorganic geochemical techniques to determine the provenance of CCA produced water as trigger for high pressure in newly drilled wells. Affinities in the hydrochemical (major, minor and trace elements) and stable isotopic (δ2H, δ18O) composition are monitored to identify single fluid types, multi-component mixing and secondary fluid alteration processes. As a proof-of-concept, geochemical fingerprints of CCA produced water from three wells were correlated with potential source candidates, i.e., utilized drilling fluids (mud filtrate, supply water) from the target well site, Early - Late Cretaceous aquifers and Late Jurassic - Late Triassic formation waters from adjacent wells and fields. Geochemical affinities of CCA water with groundwater from an Early Cretaceous aquifer postulate the presence one single horizon for active water inflow. Non-reactive elements (Na, Cl) and environmental isotopes (δ2H, δ18O) were found to be most suited tools for fluid identification. 2H/1H and 18O/16O ratios of supply water and mud filtrate are close to global meteoric water composition, whereas formation waters are enriched in 18O. Elevated SO4 and K concentrations and extreme alkaline conditions for CCA water indicates the occurrence of minor secondary alteration processes, such the contact of inflowing groundwater with cement or fluid mixing with minor portions of KCl additives. The presented technology in this study enables the detection of high CCA pressure and fluid leakages sources, thereby allowing workover engineers to plan for potential remedial actions prior to moving the rig to the affected well; hence significantly reducing operational costs. Appropriate remedial solutions can be prompted for safe well abandonment as well as to resume operation at the earliest time.

Acid Mine Drainage Sources and Impact on Groundwater at the Osarizawa Mine, Japan

Understanding the origin of acid mine drainage (AMD) in a closed mine and groundwater flow system around the mine aids in developing strategies for environmental protection and management. AMD has been continuously collected and neutralized at Osarizawa Mine, Akita Prefecture, Japan, since the mine was closed in the 1970s, to protect surrounding river water and groundwater quality. Thus, water samples were taken at the mine and surrounding groundwaters and rivers to characterize the chemical properties and environmental isotopes (δ2H and δ18O). The results showed that the quality and stable isotope ratios of AMD differed from those of groundwater/river water, indicating that the recharge areas of AMD. The recharge area of AMD was evaluated as the mountain slope at an elevation of 400–500 m while that of the surrounding groundwater was evaluated at an elevation of 350–450 m, by considering the stable isotopes ratios. This indicates that the groundwater affected by AMD is limited to the vicinity of the mine and distributed around nearby rivers.

Hydrogeochemical indications of regional flow in the Lower Greensand aquifer of the London Basin

The Lower Greensand (LGS) forms the second most important aquifer in the London Basin but, being largely absent beneath the city itself, has received much less attention than the ubiquitous overlying Chalk aquifer. While the general directions of groundwater flow in the Chalk are well established, there has been much less certainty about flow in the LGS owing to regionally sparse borehole information. This study focuses on two hitherto uncertain aspects of the confined aquifer: the sources of recharge to the west-central London Basin around Slough, and the fate of LGS water where the aquifer thins out on the flank of the London Platform in the Gravesend–Medway–Sheppey area on the southern side of the basin. The application of hydrogeochemical techniques including environmental isotopes indicates that recharge to the Slough area is derived from the northern LGS outcrop, probably supplemented by downward leakage from the Chalk, while upward leakage from the LGS in North Kent is mixing with Chalk water to the extent that some Chalk boreholes on the Isle of Sheppey are abstracting high proportions of water with an LGS fingerprint. In doing so, this study demonstrates the value of re-examining previously published data from a fresh perspective.Thematic collection: This article is part of the Hydrogeology of Sandstone collection available at: https://www.lyellcollection.org/cc/hydrogeology-of-sandstone

Hydrogeochemical and Isotopic Investigations on the Origins of Groundwater Salinization in Çarşamba Coastal Aquifer (North Turkey)

The aim of this study is to determine the origins of salinization and the main hydrogeochemical process that controls the chemistry of Çarşamba coastal aquifer in Turkey. Therefore, a total of 33 groundwater samples and three seawater samples were analyzed in the coastal region of Çarşamba Plain in July 2019 and for these samples’ physical parameters, major ions and environmental isotopes (δ18O, δ2H and 3H) values were determined. Piper, Chadha, Gibbs diagrams and Stuyfzand Classification Systems were used to determine the origins of salinization and the key hydrogeochemical process controlling the groundwater chemistry. According to Stuyfzand classification system, the study showed that the freshwater and fresh-brackish water main types are the most widespread in the study area. Six water subtypes were observed in the study area that include CaHCO3, CaMix, NaMix, NaCl, NaHCO3 and MgHCO3. In addition, the subtypes CaMix indicated the locations of the transition zone, where the groundwater rich in Ca and HCO3 and gradually enriched in Na changes from CaMix with HCO3 as dominant anion to eventually CaCl and NaCl subtypes. Furthermore, the subtypes NaMix, NaHCO3 and MgHCO3 showed the locations of the transition zone where the flushing of the saline aquifer by freshwater takes place. All groundwater samples from study area had a positive cation exchange code and show that four hydrogeochemical facies composed of CaHCO3; Ca-Mg-Cl and NaCl and NaHCO3. Besides, groundwater samples have been influenced by two main mechanisms: the water-rock interaction and evaporation-crystallization. According to δ18O, δ2H and 3H analysis, the water samples have meteoric origin, shallow circulation, and a short residence time.

Geochemical and isotopic evidence of groundwater salinization processes in the Essaouira region, north-west coast, Morocco

The city of Essaouira is located along the north-west coast of Morocco, where groundwater is the main source of drinking, domestic and agricultural water. In recent decades, the salinity of groundwater has increased, which is why geochemical techniques and environmental isotopes have been used to determine the main sources of groundwater recharge and salinization. The hydrochemical study shows that for the years 1995, 2007, 2016 and 2019, the chemical composition of groundwater in the study area consists of HCO3–Ca–Mg, Cl–Ca–Mg, SO4–Ca and Cl–Na chemical facies. The results show that from 1995 to 2019, electrical conductivity increased and that could be explained by a decrease in annual rainfall in relation to climate change and water–rock interaction processes. Geochemical and environmental isotope data show that the main geochemical mechanisms controlling the hydrochemical evolution of groundwater in the Cenomanian–Turonian aquifer are the water–rock interaction and the cation exchange process. The diagram of δ2H = 8 * δ18O + 10 shows that the isotopic contents are close or above to the Global Meteoric Water Line, which suggests that the aquifer is recharged by precipitation of Atlantic origin. In conclusion, groundwater withdrawal should be well controlled to prevent groundwater salinization and further intrusion of seawater due to the lack of annual groundwater recharge in the Essaouira region.

Hydrochemistry and environmental isotopes of spring water and their relation to structure and lithology identified with remote sensing methods in Wadi Araba, Egypt

Springs located at the historical sites of Wadi Araba (Eastern Desert of Egypt) and emerging from the escarpments of the Northern and Southern Galala Plateaus were investigated. A combination of methods, including hydrochemistry, stable and radioisotope composition, and structural analyses based on satellite data, provided information about the structure of the subsurface and the derived groundwater flow paths. Satellite images reveal karst features within the northern plateau, e.g. conical landforms. Karstic caves were documented along both escarpments. Chemical analysis of floodwater from Wadi Araba indicates higher concentrations of terrestrial salts compared to floodwaters from central and southern parts of the desert. δ18O and δ2H signatures in spring waters resemble those of floodwater and fall on the global meteoric water line, confirming their fast infiltration with minor influence of evaporation. The aquifer feeding the springs of the Northern Galala Plateau has low retention and the springs dry out quickly, even after heavy rainfall. Contrastingly, 3H activities in springs emerging from the Southern Galala Plateau refer to much slower subsurface passage. With respect to 3H content (3.8 TU) in recent flood waters, the spring water at Southern Galala Plateau contains about 40% recently recharged groundwater. However, its largest spring—the St. Antony spring—discharges water with a radiocarbon age of about 15,000 years. In combination with this spring’s constant and high discharge over a period of several months, that age estimate suggests a large reservoir with moderate to high retention.

Hydrochemistry and environmental isotopes (18O, 2H, 3H, 3He/4He) of groundwater and floodwater in the great area of Hurghada, Eastern Desert of Egypt

Porous and fractured aquifers exist in the area of Hurghada, Eastern Desert of Egypt, whose recharge processes through the common flash floods are not identified. Hydrochemical parameters, stable isotopes 18O, 2H and tritium in floodwater and groundwater were applied in the area subject to study. Additionally, He isotopes were investigated in the deep wells in the faulted zone at the Abu Shaar Plateau. 3H activity in all sampled points lies below the detection limit excluding a recent recharge component in groundwater. However, the hydrochemical ratios and the stable isotope signature confirm that the shallow wells and springs (Red Sea Hills group) are being recharged from modern precipitation. The hydrochemical parameters of the deep wells at the Abu Shaar Plateau (coastal plain group) confirm another origin for the ions rather than the modern precipitation. Together with the 18O and 2H values, the Br/Cl ratio of this group confirms the absence of seawater intrusion component and the role of the fault as a hydraulic barrier. These 18O and 2H values deviate from the GMWL confirming an evaporation effect and colder infiltration conditions and reveal strongly a possible mixing with the Nubian Sandstone in the region. The 3He/4He ratio confirms a mantle contribution of 2% from the total He components.