Correlation between geology and radon levels in groundwater, soil and indoor air in Bhilangana Valley, Garhwal Himalaya, India

 Radon concentrations were measured in soil, air and groundwater in Bhilangana Valley, Garhwal Himalaya, India by using an LR-115 plastic track detector and radon emanometer. Radon concentrations were found to vary from 1 KBq/m³ to 57 KBq/m³ in soil , 5 Bq/l to 887 Bq/l in water and 95 Bq/m³ to 208 Bq/m³ in air. The recorded values are quite high due to associated uranium mineralization in the area. Radon concentration was also found to depend on the tectonic structure and geology of the area. Received: 22 July 1996 · Accepted: 8 January 1997     

Simultaneous declines in radon and methane precursory to 2008 <Emphasis Type="Italic">M</Emphasis><Subscript>W</Subscript> 5.0 Antung earthquake: corroboration of in-situ volatilization

Radon volatilization mechanism into the gas phase was hypothesized to explain the anomalous decline in groundwater radon precursory to the 2003 M _W = 6.8 Chengkung earthquake in Taiwan. We initiated the monitoring of both radon and methane in the groundwater since November 2007 at well D1 in the Antung hot spring. The mechanism of in-situ radon volatilization has been corroborated by the simultaneous anomalous declines in groundwater-dissolved radon and methane precursory to the 2008 M _W 5.0 Antung earthquake.     

Using radon-222 to study coastal groundwater/surface-water interaction in the Crau coastal aquifer (southeastern France)

Radon has been used to determine groundwater velocity and groundwater discharge into wetlands at the southern downstream boundary of the Crau aquifer, southeastern France. This aquifer constitutes an important high-quality freshwater resource exploited for agriculture, industry and human consumption. An increase in salinity occurs close to the sea, highlighting the need to investigate the water balance and groundwater behavior. Darcy velocity was estimated using radon activities in well waters according to the Hamada “single-well method” (involving comparison with radon in groundwater in the aquifer itself). Measurements done at three depths (7, 15 and 21 m) provided velocity ranging from a few mm/day to more than 20 cm/day, with highest velocities observed at the 15-m depth. Resulting hydraulic conductivities agree with the known geology. Waters showing high radon activity and high salinity were found near the presumed shoreline at 3,000 years BP, highlighting the presence of ancient saltwater. Radon activity has also been measured in canals, rivers and ponds, to trace groundwater discharges and evaluate water balance. A model of the radon spatial evolution explains the observed radon activities. Groundwater discharge to surface water is low in pond waters (4 % of total inputs) but significant in canals (55 l/m²/day).     

Groundwater chemistry within a plateau neighboring Matsumoto city,Japan

The change in groundwater chemistry along the groundwater flow path in the Matsumoto tunnel vicinity was studied, and the origin of the groundwater and dissoluted substances was determined. The relationship between the concentration of HCO₃ ^–, Ca²⁺, and Na⁺, and CO₂ gas pressure in the groundwater indicated that the HCO₃ ^–, Ca²⁺, and Na⁺ were produced by the reaction of the CO₂ gas in the groundwater and feldspar in the rocks. The relationship between the concentration of NO₃ ^– and the Eh and pH values in the groundwater indicated that in an oxidative condition, ammonia-oxidizing and nitriteoxidizing bacteria used NH₄ ⁺ and produced NO₃ ^– and H⁺, and in a reductive condition, denitrifying bacteria used NO₃ ^– and produced N₂ gas and OH^–. The stable hydrogen and oxygen isotopic ratio in the groundwater and precipitation indicated that the groundwater originated from precipitation that had fallen on the area. The concentration of³H and the stable hydrogen and oxygen isotopic ratios in the groundwater suggested that it has been getting warmer climatically for more than 60 years. The stable carbon isotopic ratio indicated that the HCO₃ ^– in the groundwater, excluding deep well water, originated from CO₂ gas produced by organic matter in the soil. The deep well water, which had a higher concentration of HCO₃ ^– than the other groundwater sampled, was thought to have acquired HCO₃ ^– though contact with rocks. The³⁶Cl/Cl ratio indicated the recharge age of the deep well water sampled at a depth of 760 m at the foot of the plateau was recent.     

Using field analogue soil column experiments to quantify radon-222 gas migration and transport through soils and bedrock of Halifax,Nova Scotia,Canada

Radon gas is a human health hazard; long-term exposure to high radon concentrations through inhalation is the second leading cause of lung cancer. Nova Scotia has been previously identified as a potential high risk region because of the geology. As such, the gas transport through Halifax’s fine grained leucomonzogranite (FGL) unit of the South Mountain Batholith needed to be quantified to further remediation efforts. Using controlled laboratory experiments, four different soil columns were created using the Halifax Regional Municipality’s (HRM) highest producing field tills and bedrock. Permeability, diffusivity, radon-222 gas concentrations, and gas transit time/speed were measured in both dry tills (field moisture) and wet tills (simulated rain event moisture). Columns with HRM till displayed the highest radon concentrations, and were less permeable with additional moisture. Radon diffusivity calculated from CO₂ was 7.52 × 10^?8 m² (dry), and 3.37 × 10^?8 m² (wet); diffusivity calculated from ²²²Rn was 7.30 × 10^?7 m² (dry), and 6.47 × 10^?7 m² (wet). The average FGL transit time in a 60 cm column was 3.57 days (dry), and 3.82 days (wet). Locally this study presents two different methods for diffusivity calculations, for a unit lacking previous diffusivity information. The radon gas concentrations and transport speeds quantified the transport mechanisms within the till. Globally, the correlation between soil moisture, and radon/permeability values was established using these results. The link between diffusivity and permeability was also confirmed using field tills. Implications were made for building foundations, as well as the depth and type of material necessary to reduce radon gas from reaching the surface.     

Geological and tectonic influence on water–soil–radon relationship in Mandi–Manali area,Himachal Himalaya

Radon measurements in soil and groundwater (springs, thermal springs and handpumps) were made in a variety of lithological units including major thrusts between Mandi and Manali in Himachal Himalaya. Analysis of radon data in light of lithological controls and influence of deep-seated thrusts has been made to elucidate the causative factors for anomalous emanation of radon. The lithological types include banded gneisses, schists, quartzite, granite, phyllites, volcanics and mylonites. The low-grade metasedimentries of Shali and Dharamsala generally show low and narrow range of radon concentration in water (5.6–13.4 Bq/l) as well as in soil (1.8–3.2 kBq/m³) except for the samples related to thrusts. On the other hand, sheared and deformed rocks of Chail and Jutogh show moderate radon content (average 5.03 kBq/m³, range 2.9–11.1 kBq/m³) in soil. However, the groundwater radon concentration shows wide variation in different types of sources (2.1–80.8 Bq/l). The quartzite and volcanic rocks of Rampur formation in this area present as a window separated by Chail thrust. Radon emanations on these rock types are relatively high (6.3–68.1 Bq/l in water and 5.5–15.9 kBq/m³ in soil) and are exceptionally high in samples that are related to uranium mineralization, deep-seated thrusts and hot springs (13.5–653.5 Bq/l). It is generally observed that anomalous high radon content is associated with mineralization, deeper source and tectonic discontinuities. Whereas it is obvious that subsurface radioactive mineralization would facilitate enhanced radon production, however, thrust plains provide easy pathways for escape of gases from the deeper sources. Shallow and deep sources of the groundwater have contrasting radon content particularly in the deformed and metamorphosed rocks of Jutogh and Chail. Shallow groundwater sources, mainly handpumps, have lower radon concentration due to limited superficial water circulation, whereas deeper sources, mainly perennial springs, show higher radon content because of larger opportunity for water–rock interaction.     

Assessing groundwater-surface water connectivity using radon and major ions prior to coal seam gas development (Richmond River Catchment,Australia)

Coal seam gas (CSG, or coal bed methane) mining is rapidly growing, with poorly understood impacts on groundwater and surface water systems. Here, we use chemical tracers to investigate groundwater-surface water connectivity in an Australian river system (Richmond River Catchment, New South Wales) prior to CSG extraction but after ∼ 50 exploratory CSG wells were drilled. We performed four surveys of 29 interconnected creek and river sites, over contrasting hydrological conditions. Radon was used to determine if a surface water segment was gaining groundwater. Radon observations over four seasons revealed that 28 out of 77 surface water segments were clearly gaining groundwater, 5 were possibly gaining groundwater and 44 were undetermined. This is equivalent to gaining segments in 333 km (39%) of surface water from the 864 km being investigated. High spatial and temporal variability in groundwater gaining segments was found. Na/Cl ratios were used to determine the fraction of groundwater in surface water. Overall, the groundwater contribution in surface waters was 14–24% higher in post flood conditions than during the other three surveys of baseflow and moderate flow conditions. The results serve as a regional baseline assessment of river water chemistry and groundwater-surface water connectivity prior to the planned development of CSG fields. Our geochemical tracer approach allows for a quick qualitative assessment of groundwater-surface water connectivity in poorly gauged river systems and can define priority locations where groundwater extraction for CSG mining should be carefully managed.     

Noble gas tracing of groundwater/coalbed methane interaction in the San Juan Basin, USA

The San Juan Basin natural gas field, located in northwestern New Mexico and southwestern Colorado in the USA, is a case-type coalbed methane system. Groundwater is thought to play a key role in both biogenic methane generation and the CO₂ sequestration potential of coalbed systems. We show here how noble gases can be used to construct a physical model that describes the interaction between the groundwater system and the produced gas. We collected 28 gas samples from producing wells in the artesian overpressured high production region of the basin together with 8 gas samples from the underpressured low production zone as a control. Stable isotope and major species determination clearly characterize the gas in the high production region as dominantly biogenic in origin, and the underpressured low producing region as having a significant admix of thermogenic coal gas. ³He/⁴He ratios increase from 0.0836R_a at the basin margin to 0.318R_a towards the center, indicating a clear but small mantle He signature in all gases. Coherent fractionation of water-derived ²⁰Ne/³⁶Ar and crustal ⁴He/⁴⁰Ar* are explained by a simple Rayleigh fractionation model of open system groundwater degassing. Low ²⁰Ne concentrations compared to the model predicted values are accounted for by dilution of the groundwater-associated gas by desorbed coalbed methane. This Rayleigh fractionation and dilution model together with the gas production history allows us to quantify the amount of water involved in gas production at each well. The quantified water volumes in both underpressured and overpressured zones range from 1.7 × 10³ m³ to 4.2 × 10⁵ m³, with no clear distinction between over- and underpressured production zones. These results conclusively show that the volume of groundwater seen by coal does not play a role in determining the volume of methane produced by secondary biodegradation of these coalbeds. There is no requirement of continuous groundwater flow for renewing the microbes or nutrient components. We furthermore observe strong mass related isotopic fractionation of ²⁰Ne/²²Ne and ³⁸Ar/³⁶Ar isotopic ratios. This can be explained by a noble gas concentration gradient in the groundwater during gas production, which causes diffusive partial re-equilibration of the noble gas isotopes. It is important for the study of other systems in which extensive groundwater degassing may have occurred to recognize that severe isotopic fractionation of air-derived noble gases can occur when such concentration gradients are established during gas production. Excess air-derived Xe and Kr in our samples are shown to be related to the diluting coalbed methane and can only be accounted for if Xe and Kr are preferentially and volumetrically trapped within the coal matrix and released during biodegradation to form CH₄.     

An 8-year record of gas geochemistry and isotopic composition of methane during baseline sampling at a groundwater observation well in Alberta (Canada)

Variability in baseline groundwater methane concentrations and isotopic compositions was assessed while comparing free and dissolved gas sampling approaches for a groundwater monitoring well in Alberta (Canada) over an 8-year period. Methane concentrations in dissolved gas samples (n?=?12) were on average 4,380?±?2,452 μg/L, yielding a coefficient of variation (CV) >50 %. Methane concentrations in free gas samples (n?=?12) were on average 228,756?±?62,498 ppm by volume, yielding a CV of 27 %. Quantification of combined sampling, sample handling and analytical uncertainties was assessed via triplicate sampling (CV of 19 % and 12 % for free gas and dissolved gas methane concentrations, respectively). Free and dissolved gas samples yielded comparable methane concentration patterns and there was evidence that sampling operations and pumping rates had a marked influence on the obtained methane concentrations in free gas. δ¹³C_CH4 and δ²H_CH4 values of methane were essentially constant (?78.6?±?1.3 and ?300?±?3?‰, respectively) throughout the observation period, suggesting that methane was derived from the same biogenic source irrespective of methane concentration variations. The isotopic composition of methane constitutes a robust and highly valuable baseline parameter and increasing δ¹³C_CH4 and δ²H_CH4 values during repeat sampling may indicate influx of thermogenic methane. Careful sampling and analytical procedures with identical and repeatable approaches are required in baseline-monitoring programs to generate methane concentration and isotope data for groundwater that can be reliably compared to repeat measurements once potential impact from oil and gas development, for example, may occur.     

In situ feldspar dissolution rates in an aquifer

In situ silicate dissolution rates within the saturated Navajo sandstone, at Black Mesa, Arizona were determined from elemental fluxes in the aquifer. The mass transfer between groundwater and mineral matrix along flow paths was calculated from inverse mass balance modeling. The reaction time is bound by ¹⁴C-based travel time. BET surface areas were measured with N₂ gas adsorption. Dissolution rates for K-feldspar and plagioclase are 10⁻¹⁹ and 10⁻¹⁶ mol (feldspar) m⁻² s⁻¹, respectively, which are ∼10⁵ times slower than laboratory experiment-derived rates under similar pH and temperature but at far from equilibrium conditions. The rates obtained in this study are consistent with the slower field rates found in numerous watershed and soil profile studies. However, these rates are from saturated aquifers, overcoming some concerns on estimated rates from unsaturated systems. The Navajo sandstone is a quartz-sandstone with a relatively simple and well-studied hydrogeology, groundwater geochemistry, and lithology, a large number of groundwater analyses and ¹⁴C groundwater ages, groundwater residence times up to ∼37 ky, groundwater pH from ∼8 to 10, and temperature from ∼15 to 35°C.     

Chemical and isotope compositions of shallow groundwater in areas impacted by hydraulic fracturing and surface mining in the Central Appalachian Basin,Eastern United States

Hydraulic fracturing of shale deposits has greatly increased the productivity of the natural gas industry by allowing it to exploit previously inaccessible reservoirs. Previous research has demonstrated that this practice has the potential to contaminate shallow aquifers with methane (CH₄) from deeper formations. This study compares concentrations and isotopic compositions of CH₄ sampled from domestic groundwater wells in Letcher County, Eastern Kentucky in order to characterize its occurrence and origins in relation to both neighboring hydraulically fractured natural gas wells and surface coal mines. The studied groundwater showed concentrations of CH₄ ranging from 0.05 mg/L to 10 mg/L, thus, no immediate remediation is required. The δ¹³C values of CH₄ ranged from −66‰ to −16‰, and δ²H values ranged from −286‰ to −86‰, suggesting an immature thermogenic and mixed biogenic/thermogenic origin. The occurrence of CH₄ was not correlated with proximity to hydraulically fractured natural gas wells. Generally, CH₄ occurrence corresponded with groundwater abundant in Na⁺, Cl⁻, and HCO₃⁻, and with low concentrations of SO₄²⁻. The CH₄ and SO₄²⁻concentrations were best predicted by the oxidation/reduction potential of the studied groundwater. CH₄ was abundant in more reducing waters, and SO₄²⁻ was abundant in more oxidizing waters. Additionally, groundwater in greater proximity to surface mining was more likely to be oxidized. This, in turn, might have increased the likelihood of CH₄ oxidation in shallow groundwater.     

Analysis of the exchange of groundwater and river water by using Radon-222 in the middle Heihe Basin of northwestern China

In arid regions of western China, water resources come from mountain watersheds and disappear in the desert plain. The exchange of surface water and groundwater takes place two or three times in a basin. It is essential to analyze the interaction of groundwater with surface water to use water resources effectively and predict the change in the water environment. The conventional method of analysis, however, measures only the flow of a stream and cannot determine groundwater seepage accurately. As the concentration of Radon-222 (²²²Rn) in groundwater is much higher than in surface water, the use of ²²²Rn was examined as an indicator for the analysis of the interaction between surface water and groundwater. Measurement of the ²²²Rn concentration in surface water was conducted to detect groundwater seepage into a stream in the middle Heihe Basin of northwestern China. Furthermore, the simultaneous groundwater flow into and out of a stream from the aquifers was quantified by solving the ²²²Rn mass balance equation, in which the losses of gas exchange and radioactive decay of ²²²Rn are considered. Meanwhile, river runoff was gauged to determine the exchange rates between surface water and groundwater. The result shows that ²²²Rn isotope can be used as a good environmental tracer with high sensitivity for the interaction between surface water and groundwater, especially in the fractured aquifer system, karst aquifer system and discharge basins.     

Origin and recharge estimates of groundwater in the ordos plateau,People’s Republic of China

Groundwater is a valuable resource in the semiarid Ordos Plateau region where abundant mineral resources, such as coal, natural gas, and halite, are present. With resources development, groundwater demand will increase dramatically. The origin identification and recharge estimates of groundwater are significant components of sustainable groundwater development in the Ordos Plateau. Groundwater and precipitation samples were taken and the isotopic compositions δ²H, δ¹⁸O, and chloride were analyzed to identify groundwater origins and to estimate recharge rates. The δ²H and δ¹⁸O of the groundwater show that the groundwater recharge is of meteoric origin. The chloride mass balance (CMB) method was used to quantify recharge rates of groundwater in the Ordos Plateau, which varies from 2.93 to 22.11% of the effective annual rainfall. Recharge rates estimated by CMB were compared with values obtained from other methods and were found to be in good agreement. This study can be used to develop effective programs for groundwater management and development.     

Spatial distribution mapping and radiological hazard assessment of groundwater and soil gas radon in Ekiti State,Southwest Nigeria

Groundwater constitutes the major source of utility water in Ekiti State with the majority of the population depending on groundwater for drinking and other household uses. Soil in the area is commonly used as a component of building materials, which may produce radon in the indoor environment. Excessive concentrations of radon in water and soil can cause radiological health risks to human as witnessed by the increased cases of lung cancer among non-smokers in Nigeria, which may be traceable to the ingestion and inhalation ²²²Rn in drinking water and indoor air. In the present study, comparative in situ measurements of radon in groundwater and soil gas were carried out at one hundred selected locations across the Ekiti State in southwest Nigeria, using a RAD7 radon detector to generate a radon distribution map and to estimate radiation hazards due to radon. The concentrations of radon in groundwater ranged from 0.9 to 472 Bq L^?1 with a mean of 34.7?±?4.4 Bq L^?1, while those of soil gas ranged from 0.1 to 315 kBq L^?1 with a mean of 38.9?±?1.4 kBq L^?1. The total annual effective dose due to inhalation and ingestion of radon in groundwater amounted to 94.7 µSv year^?1, which is lower than the reference dose of 100 µSv year^?1 recommended by the World Health Organization (WHO). The radon map generated for groundwater and soil gas identified three distinct areas with radon levels ranging from low to high. The results of this study show that some locations (Emure, Gbonyin, Ijero and Ikole) show mean total annual effective doses which are higher than the recommended limit. It can then be inferred that the groundwater samples pose significant radiological hazards to the population and that the noticed increase in lung cancer cases may be attributed to the consumption of groundwater in the area.     

Tracing the sources of strontium in karst groundwater in Chongqing, China: a combined hydrogeochemical approach and strontium isotope

Groundwater quality in karst regions is largely controlled by natural processes and anthropogenic activities. Over the past 10?years, dissolved Sr and its radiogenic isotope, ⁸⁷Sr/⁸⁶Sr, were widely used to trace the sources of solutes in groundwater. However, there is little research about hydrogeochemistry and Sr isotopic compositions of the karst groundwater in Chongqing karst area. In this paper, thirty-five representative karst groundwater samples were collected from different aquifers (limestone and dolomite) and various land use types. Hydrochemical types of karst groundwater in Chongqing were mainly of the Ca-HCO₃ type or Ca(Mg)-HCO₃ type. The dissolved Sr concentrations of the studied groundwater ranged from 0.57 to 15.06???mmol/L, and the ⁸⁷Sr/⁸⁶Sr varied from 0.70751 to 0.71627. The groundwater samples from different aquifers and land use types showed distinctive dissolved Sr concentrations and ⁸⁷Sr/⁸⁶Sr. The very positive relationship between Ca/Sr and Mg/Sr in dolomite and limestone aquifers suggests that Ca, Mg and Sr element come mainly from the release of carbonate rock under the groundwater?Crock?CCO₂ gas interaction. According to the ⁸⁷Sr/⁸⁶Sr ratio, the Sr element in karst groundwater in Chongqing was controlled by the weathering of limestone, dolomite and silicate rock (allogenic water in a non-karst area). The relationship ⁸⁷Sr/⁸⁶Sr versus Sr²⁺/[K⁺?+?Na⁺] shows that the anthropogenic inputs also obviously contribute to the Sr contents. The research results show that the karst groundwater in Chongqing is facing serious crisis of water quality, and needs to be protected further.     

Radioactive elements in natural gas: a case study on distribution of gaseous 222radon and its origin mechanism

As natural gas becomes increasingly important in our daily life, studies have been carried out on trace elements such as mercury and arsenic within it. Other than those, the existence of radioactive gaseous radon from the combustion of natural gas indoors can cause severe diseases and damages to body organs, putting a hazardous impact on human health. At the same time, the radon can also corrode gas production and transportation equipment. A review of the literature on radon concentrations in natural gas produced from gas reservoirs in China and other countries have been studied. Radon is a decay product from ²³⁸U, which is closely related to the accumulation and migration of organic matter during diagenesis. Gas recovered from reservoirs with higher than average natural ²³⁸U contains higher than average levels of ²²²Rn. Massive fault systems and fracture zones appear to play a significant role in radon concentrations in natural gas.     

Carbon and hydrogen isotopic evidence for the origin of combustible gases in water-supply wells in north-central Pennsylvania

The origin of the combustible gases in groundwater from glacial-outwash and fractured-bedrock aquifers was investigated in northern Tioga County, Pennsylvania. Thermogenic methane (CH₄) and ethane (C₂H₆) and microbial CH₄ were found. Microbial CH₄ is from natural in situ processes in the shale bedrock and occurs chiefly in the bedrock aquifer. The δ¹³C values of CH₄ and C₂H₆ for the majority of thermogenic gases from water wells either matched or were between values for the samples of non-native storage-field gas from injection wells and the samples of gas from storage-field observation wells. Traces of C₂H₆ with microbial CH₄ and a range of C and H isotopic compositions of CH₄ indicate gases of different origins are mixing in sub-surface pathways; gas mixtures are present in groundwater. Pathways for gas migration and a specific source of the gases were not identified. Processes responsible for the presence of microbial gases in groundwater could be elucidated with further geochemical study.     

Carbon and hydrogen isotopic evidence for the origin of combustible gases in water-supply wells in north-central Pennsylvania

The origin of the combustible gases in groundwater from glacial-outwash and fractured-bedrock aquifers was investigated in northern Tioga County, Pennsylvania. Thermogenic methane (CH₄) and ethane (C₂H₆) and microbial CH₄ were found. Microbial CH₄ is from natural in situ processes in the shale bedrock and occurs chiefly in the bedrock aquifer. The δ¹³C values of CH₄ and C₂H₆ for the majority of thermogenic gases from water wells either matched or were between values for the samples of non-native storage-field gas from injection wells and the samples of gas from storage-field observation wells. Traces of C₂H₆ with microbial CH₄ and a range of C and H isotopic compositions of CH₄ indicate gases of different origins are mixing in sub-surface pathways; gas mixtures are present in groundwater. Pathways for gas migration and a specific source of the gases were not identified. Processes responsible for the presence of microbial gases in groundwater could be elucidated with further geochemical study.     

The noble gas geochemistry of natural CO2 gas reservoirs from the Colorado Plateau and Rocky Mountain provinces, USA

Identification of the source of CO₂ in natural reservoirs and development of physical models to account for the migration and interaction of this CO₂ with the groundwater is essential for developing a quantitative understanding of the long term storage potential of CO₂ in the subsurface. We present the results of 57 noble gas determinations in CO₂ rich fields (>82%) from three natural reservoirs to the east of the Colorado Plateau uplift province, USA (Bravo Dome, NM., Sheep Mountain, CO. and McCallum Dome, CO.), and from two reservoirs from within the uplift area (St. John’s Dome, AZ., and McElmo Dome, CO.). We demonstrate that all fields have CO₂/³He ratios consistent with a dominantly magmatic source. The most recent volcanics in the province date from 8 to 10 ka and are associated with the Bravo Dome field. The oldest magmatic activity dates from 42 to 70 Ma and is associated with the McElmo Dome field, located in the tectonically stable centre of the Colorado Plateau: CO₂ can be stored within the subsurface on a millennia timescale.The manner and extent of contact of the CO₂ phase with the groundwater system is a critical parameter in using these systems as natural analogues for geological storage of anthropogenic CO₂. We show that coherent fractionation of groundwater ²⁰Ne/³⁶Ar with crustal radiogenic noble gases (⁴He, ²¹Ne, ⁴⁰Ar) is explained by a two stage re-dissolution model: Stage 1: Magmatic CO₂ injection into the groundwater system strips dissolved air-derived noble gases (ASW) and accumulated crustal/radiogenic noble gas by CO₂/water phase partitioning. The CO₂ containing the groundwater stripped gases provides the first reservoir fluid charge. Subsequent charges of CO₂ provide no more ASW or crustal noble gases, and serve only to dilute the original ASW and crustal noble gas rich CO₂. Reservoir scale preservation of concentration gradients in ASW-derived noble gases thus provide CO₂ filling direction. This is seen in the Bravo Dome and St. John’s Dome fields. Stage 2: The noble gases re-dissolve into any available gas stripped groundwater. This is modeled as a Rayleigh distillation process and enables us to quantify for each sample: (1) the volume of groundwater originally ‘stripped’ on reservoir filling; and (2) the volume of groundwater involved in subsequent interaction. The original water volume that is gas stripped varies from as low as 0.0005 cm³ groundwater/cm³ gas (STP) in one Bravo Dome sample, to 2.56 cm³ groundwater/cm³ gas (STP) in a St. John’s Dome sample. Subsequent gas/groundwater equilibration varies within all fields, each showing a similar range, from zero to ∼100 cm³ water/cm³ gas (at reservoir pressure and temperature).     

Determination of groundwater recharge regime and flowpath in the Lower Heihe River basin in an arid area of Northwest China by using environmental tracers: Implications for vegetation degradation in the Ejina Oasis

Environmental tracers (CFCs, stable isotopes ¹⁸O, ²H, and ³H) and major ions were employed to study river infiltration and groundwater recharge in the aquifer system in the basin of the Lower Heihe River, Northwest China. Three groups of waters have been recognized: (1) young groundwater, connected to the river, with large variation of CFC apparent ages ranging from <10 a to 40 a, and δ¹⁸O and δ²H values which are similar to the river water; (2) regional background water, unaffected by the river, having CFC apparent ages >40 a, and being depleted in ¹⁸O and ²H compared with the river water; and (3) groundwater in Gurinai, a grassland located about 100 km from the river, in which the predominant discharge is from the Badain Jaran desert, with CFC apparent ages ranging from 25 to >50 a and being enriched in ¹⁸O and ²H compared to the river water. The groundwater along the river contains CFCs and ³H down to depths of about 120 m, and the shallow groundwater exhibits CFC apparent ages in a wide range which are not dependent on the well depth. Groundwaters along the river show a similar trend of enrichment in ¹⁸O and ²H as the river water whereas groundwaters in depression cones are depleted in heavier isotopes, and have low CFC and ³H concentrations. The CFC apparent age of the groundwater increases with increasing distance downstream, indicating that the dominant part of the groundwater is from infiltration of river water in the upper reaches. Modifications of groundwater recharge are reflected in variations of stable isotope compositions, as well as CFC and ³H concentrations in the groundwater that was recharged from the river over the last decades. Despite recharging from river water, groundwater abstraction has induced a water balance deficit. The riparian ecosystem in the Ejina Oasis is constrained by both decreased river flow and increased groundwater abstraction. The vegetation degradation in the Ejina Oasis is controlled not only by natural aridification but also worsened by heavy groundwater abstraction and decreased river flow.