Uranium isotopes as a tracer of sources of dissolved solutes in the Han River,South Korea

The uranium (U) content and ²³⁴U/²³⁸U activity ratio were determined for water samples collected from Korea's Han River in spring, summer, and winter 2006 to provide data that might constrain the origin of U isotope fractionation in river water and the link between U isotope systematics in river waters and the lithological nature of the corresponding bedrock. The large difference in the major dissolved loads between the two major branches of the Han River, the North Han River (NHR) and South Han River (SHR), is reflected in the contrasting U content and ²³⁴U/²³⁸U activity ratio between the tributaries: low U content (0.08–0.75 nM; average, 0.34 nM) and small ²³⁴U/²³⁸U activity ratio (1.03–1.22; average, 1.09) in the NHR; and high U content (0.65–1.98 nM; average, 1.44 nM) and large ²³⁴U/²³⁸U activity ratio (1.05–1.45; average, 1.24) in the SHR. The large spatial differences in U content and ²³⁴U/²³⁸U activity ratio are closely related to both lithological differences between the two tributaries and groundwater input. The low U content and small ²³⁴U/²³⁸U activity ratio in the NHR arise mainly from a combination of surface and meteoric weathering of the dominant silicate rocks in this branch and congruent dissolution of already weathered (secular equilibrium) materials. In contrast, the high U content and large ²³⁴U/²³⁸U activity ratio in the SHR are ascribed to the dissolution of carbonates and black shales along with significant inputs of deep groundwater.     

Use of the subsurface thermal regime as a groundwater-flow tracer in the semi-arid western Nile Delta,Egypt

Temperature profiles from 25 boreholes were used to understand the spatial and vertical groundwater flow systems in the Western Nile Delta region of Egypt, as a case study of a semi-arid region. The study area is located between the Nile River and Wadi El Natrun. The recharge areas, which are located in the northeastern and the northwestern parts of the study area, have low subsurface temperatures. The discharge areas, which are located in the western (Wadi El Natrun) and southern (Moghra aquifer) parts of the study area, have higher subsurface temperatures. In the deeper zones, the effects of faults and the recharge area in the northeastern direction disappear at 80 m below sea level. For that depth, one main recharge and one main discharge area are recognized. The recharge area is located to the north in the Quaternary aquifer, and the discharge area is located to the south in the Miocene aquifer. Two-dimensional groundwater-flow and heat-transport models reveal that the sealing faults are the major factor disturbing the regional subsurface thermal regime in the study area. Besides the main recharge and discharge areas, the low permeability of the faults creates local discharge areas in its up-throw side and local recharge areas in its down-throw side. The estimated average linear groundwater velocity in the recharge area is 0.9 mm/day to the eastern direction and 14 mm/day to the northwest. The average linear groundwater discharge velocities range from 0.4 to 0.9 mm/day in the southern part.     

Characterising the distribution of near-shore submarine groundwater discharge along a coastline using 222Rn and electrical conductivity

The spatial and temporal distribution of near-shore fresh submarine groundwater discharge (SGD) was characterised from the coastal aquifers of the Willunga Basin, South Australia, an extensive aquifer system that supports an important viticultural region. Measurements of electrical conductivity (EC) and ²²²Rn (radon) activity were collected at 19 sites along the coastline during the Southern Hemisphere spring (2011) and summer (2013). At each site, samples were collected from the surf zone as well asporewater from beach sediment in the intertidal zone. Surf-zone radon activity ranged from <5 to 70mBq L^–1, and intertidal porewater radon ranged over two orders of magnitude (220–36 940 mBq L^–1) along the Willunga Basin coastline during both surveys. Overall, surf-zone and porewater EC was lower in the spring 2011 survey than in the summer 2013 survey. Porewater EC was similar to that of coastal water at most sites along the coastline, except at three sites where porewater EC was found to be lower than coastal water during both surveys, and three sites where evaporated seawater was observed in the summer survey. Based on the patterns in radon and EC along the coastline, two sites of localised fresh SGD were identified, in addition to a groundwater spring that is known to discharge to the coast. The results indicate that near-shore fresh SGD occurs as localised seeps rather than diffuse seepage along the entire coastline. The apparent absence of groundwater discharge at most locations is also consistent with current evidence suggesting that extensive groundwater pumping within the basin has resulted in seawater intrusion across much of the coastline. These observations also suggest that previous studies are likely to have over-estimated SGD rates from the Willunga Basin because they assumed that SGD occurred along the entire coastline.     

Rare-earth element geochemistry as a tracer for clarifying the provenance of the stream sediments in Namhan River, Korea

In the last forty years, the rare-earth elements （REEs） have been used as a powerful tool for solving various geological and geochemical problems due to their unique and chemically coherent behavior. The river sediments are produced by weathering, transportation and deposition. Nesbitt suggested that the rare-earth elements had been mobilized and fractionated during supracrustal alteration of the Torrongo granite, southeastern Australia. Nevertheless, recently, our replicate estimation for REE patterns in sediments revealed that there is nearly no variation in REE patterns. This suggests that invariability of REE patterns in weathering and solidification can be used as a tracer for constraining the provenance of stream sediments. In order to trace the pathway of the river sediments geochemically, based on the REE geochemistry from the river sediments and rocks, we have monitored the REE abundance of stream sediments at branch rivers of the Namhan River in South Korea for three years. The branches studied are Bokhacheon, Shinduncheon and Yanghwacheon. The sediments were divided into coarse （〉300 μm） and fine fractions （〈300 μm）. As a result, we could observe that major element compositions were similar to each other regardless of particle size and sampling date. This suggests that it is difficult to deduce a geochemical difference between river sediments based on major element composition and particle size. The geochemical characteristics of surrounding soils were similar to those of fine river sediments. And the chondrite-normalized REE patterns of most of the fine and coarse sediments in combination with grain sizes and drainage area showed very close relationship with the surrounding rocks. However, some sites showed that there were large variations in REE patterns including total REE abundance and Eu anomaly due to feldspars. This variation trend of REE patterns suggests that changes might have happened in sediment supply for the drainage system in the study area due to floods or large-scale construction.     

Calculations of horizontal mixing rates using222Rn and the controls on hypoxia in western Long Island Sound, 1991

Late summer hypoxia (<3 ppm oxygen) in western Long Island Sound (WLIS) is a persistent environmental and management issue whose controlling processes are poorly understood. Measured rates of sediment and water-column oxygen consumption in the bottom water suggest that a condition of no oxygen should be attained on the time scale of 13–30 d. Observations, however, indicate the onset of hypoxia is of the order 150 d. Therefore, horizontal and/or vertical transport of oxygen into the area of hypoxia must play an important role. Hypoxia decreases benthic activity and the sediment flux of²²²Rn. The resulting horizontal gradient in bottom water²²²Rn was measured and used to estimate the effective horizontal transport rate (>5–50 m² s^?1), which is considerably slower than previous estimates. Scale analysis of the hypoxia process indicates that horizontal transport rates alone can explain the slow progression of hypoxia in XLIS but that vertical processes may also be capable of delaying the onset of hypoxia especially under conditions of weak stratification or weak intermediate layer oxygen consumption. This scale analysis indicates a delicately balanced process that is sensitive to both climatologically-driven variability in the rates of horizontal and vertical transport as well as the biologically-driven rates of oxygen consumption. An improved ability to predict and/or control hypoxia must be based on a better understanding of temporal and spacial variations in circulation, mixing, and stratification as well as the biological processes in the water column and the sediments.     

Simulation of DNAPL infiltration and spreading behaviour in the saturated zone at varying flow velocities and alternating subsurface geometries

The influence of varying groundwater flow velocities on DNAPL infiltration and spreading behaviour was investigated by multiphase modelling using TMVOC and PetraSim. The multiphase models were calibrated by results of previously conducted laboratory experiments for the complete spatio-temporal range of the experiments. The small scale 2D scenario modelling was applied to qualify and quantify changes in position, architecture, geometry and dissolution of a TCE body in a fully saturated homogeneous sandy medium. The applied flow velocities ranging from 0.05 up to 40.00 m/day exhibited that the DNAPL TCE is affected even at the lowest flow velocity in its position, its size and its architecture. Additionally, several impermeable lenses with simple geometry were assumed in the model, to investigate the influence of stratified subsoil. In the experimental set-ups, the DNAPL body reacts more sensitive to the applied groundwater flow velocities than to the geometrical set-up of the scenarios. A possible consequence can be the transportation and displacement of a DNAPL pool due to natural or anthropogenic induced high groundwater flow velocities, as by Pump and Treat facilities, complicating site investigation process and planning of remediation activities.     

The oxygen isotopic composition of phosphate as an effective tracer for phosphate sources in Hongfeng Lake

In order to characterize the oxygen isotopic composition of internal phosphate and explore the possibility of using these data to identify phosphate sources, we measured oxygen isotopic compositions of phosphate (δ¹⁸O_p) in sediment pore water in Hongfeng Lake, a typical deep-water lake in a mountainous area. These data, in combination with δ¹⁸O_p in surface water samples and water column samples, were successfully used to identify phosphate sources. The δ¹⁸O_p value of sediment pore water ranged from 15.2‰ to 15.8‰, with an average value of 15.5‰—the δ¹⁸O_p value of internal phosphate. The δ¹⁸O_p values decreased gradually through the water column from 19.4‰ in surface water to 16.4‰ in deeper water, implying that internal phosphate had more negative δ¹⁸O_p values than external phosphate. This finding was substantiated by horizontal variations in δ¹⁸O_P values, which decreased with increasing distance from inflowing rivers. All collected evidence suggests that external and internal phosphate have distinctly different isotopic signatures and that these signatures have not been considerably altered by biological mediation in Hongfeng Lake. Therefore, δ¹⁸O_P can be used to distinguish phosphate sources. A two-endmember mixing model showed that internal phosphate had an average contribution of 40%, highlighting the influence of internal phosphorus loading on aqueous phosphate and eutrophication. This study illustrates the need to reduce the internal phosphorus load from sediment and provides guidance for nutrient management and in-lake restoration treatment in Hongfeng Lake. The data presented here are limited, but serve to highlight the great potential of δ¹⁸O_p as an effective tracer for identifying phosphate sources. Systematic investigations of the oxygen isotopic compositions of external phosphate, internal phosphate, and phosphate through the water column, in combination with in-lake P biogeochemical cycle study, would be desirable in further research.     

Nitrogen geochemistry as a tracer of fluid flow in a hydrothermal vent complex in the Karoo Basin, South Africa

We have investigated the N geochemistry of minerals and rocks from contact metamorphic aureoles and hydrothermal vent complexes (HVC) in the Karoo Basin in South Africa. The HVC formed during phreatic eruptions associated with rapid devolatilization and pressure build-up in contact aureoles around early Jurassic sill intrusions. By combining outcrop data from a HVC and core data from contact aureoles, we investigate the relationship between light element release during metamorphism and vertical fluid migration. Sandstone and breccia from the HVC contain early-diagenetic ammonium -bearing feldspar (buddingtonite) and illite. Ammonium occupies up to 95% of the A site in feldspar, corresponding to concentrations up to 5.2 wt% N. Bulk-rock N isotope data for rocks from inside and outside the hydrothermal vent complex fall into two distinct groups. Background samples have δ¹⁵N_air between +1.5‰ and +4.9‰, whereas minerals from the vent complex have δ¹⁵N in the range +7.5 to +10.6‰. The N geochemistry of contact metamorphic shale from the lower stratigraphic units of the Karoo Basin shows that the vitrinite reflectance and δ¹⁵N values are positively correlated. Shale with reflectivity values >4%Ro are enriched in ¹⁵N, with δ¹⁵N values between +6‰ and +14‰, implying the release of isotopically light N into metamorphic fluids (probably as N₂). We suggest that the relatively high δ¹⁵N values of the early-diagenetic buddingtonite in the HVC reflect exchange of buddingtonite with N-bearing fluids ascending from greater depth after their release during contact metamorphism and dehydration. We present a qualitative model whereby hydrothermal vent complexes represent fluid flow structures after their formation, focusing N-bearing metamorphic fluids sourced in deeper levels of the basin. The release of organic N from sediments at depth in volcanic basins could play a role in the geochemical cycle of N, becoming particularly important during periods of intense volcanic activity.     

Assessment of groundwater chemistry in a coastal region (Kunsan, Korea) having complex contaminant sources: a stoichiometric approach

Groundwater chemistry in a coastal region (Kunsan, Korea) having complex contaminant sources was investigated. Water analysis data for 197 groundwater samples collected from the uniformly distributed sixty-six wells were used. Chemical analysis results indicate that groundwaters show wide concentration ranges in major inorganic ions, reflecting complex hydrochemical processes. Due to the complexity of groundwater chemistry, the samples were classified into four groups based on Cl and NO₃ concentrations and the processes controlling water chemistry were evaluated based on the reaction stoichiometry. The results explained the importance of mineral weathering, anthropogenic activities (nitrification and oxidation of organic matters), and Cl-salt inputs (seawater, deicer, NaCl, etc.) on groundwater chemistry. It was revealed that mineral dissolution is the major process controlling the water chemistry of the low Cl and NO₃ group (Group 1). Groundwaters high in NO₃ (Groups 2 and 4) are acidic in nature, and their chemistry is largely influenced by nitrification, oxidation of organic matters and mineral dissolution. In the case of chloride rich waters (Group 3), groundwater chemistry is highly influenced by mineral weathering and seawater intrusion associated with cation-exchange reactions.     

Simultaneous monitoring of soil 222Rn in the Eastern Himalayas and the geothermal region of eastern India: an earthquake precursor

Natural Hazards - Activity of 222Rn gas in soil has been recorded continuously at three monitoring centres, namely Ravangla and Diphu in the Eastern Himalayan region and Tantloi in the geothermal...     

Ra and Rn isotopes as natural tracers of submarine groundwater discharge in the patagonian coastal zone (Argentina): an initial assessment

Submarine groundwater discharge (SGD) is herein recognized as a significant pathway of material transport from land to the coastal SW Atlantic Ocean and thus, it can be a relevant factor affecting the marine biogeochemical cycles in the region. This paper focuses on the initial measurements of ²²⁶Ra, ²²⁸Ra and ²²²Rn made in Patagonia’s coastal zone of Chubut and Santa Cruz provinces (42°S–48°S, Argentina). ²²⁶Ra activity ranged from 2.9 to 73.5 dpm 100 L^?1, and ²²⁸Ra activity ranged from 11.9 to 311.0 dpm 100 L^?1 in groundwater wells. The radium activities found in Patagonia’s marine coastal regions and adjacent shelf indicate significant enrichment throughout the coastal waters. Groundwater samples presented the largest ²²²Rn activity and ranged from 2.66 to 1083 dpm L^?1. Conversely, in the coastal marine environment, the ²²²Rn activity ranged from 1.03 to 6.23 dpm L^?1. The Patagonian coastal aquifer showed a larger enrichment in ²²⁸Ra than in ²²⁶Ra, which is a typical feature for sites where SGD is dominant, probably playing a significant role in the biogeochemistry of these coastal waters.     

Identification of sources affecting water chemistry in the Nakdong River,South Korea

The sources impacting the water chemistry of the Nakdong River (NR) in South Korea were investigated in order to examine the pollution mechanism including the fate and transport of the contaminants and how much such sources may affect its main channel of water resource. Water samples were collected between 2007 and 2008 from 8 sites along a 510 km downstream transect of the NR, and chemical and isotopic compositions of the water samples were evaluated to identify natural and anthropogenic sources contributing to the water chemistry of the NR. The results showed that the major ion concentrations were mainly controlled by chemical weathering that occurred in the watershed, in which a silicate weathering is more dominant than a carbonate weathering. The ⁸⁷Sr/⁸⁶Sr ratios of the water samples were in a range from 0.71043 to 0.71520 within those of the Mesozoic volcanogenic sedimentary rocks long developed in the watershed, thereby supporting the fact that the water chemistry is governed by a chemical weathering. The δ³⁴S values varied in a narrow range of 1.8–3.1‰, regardless of spatial and seasonal variations. Mass balance calculations indicated that the contributions of chemical weathering and anthropogenic sources during summer time increased along a downstream transect, from 67.3 ± 1.3 to 73.6 ± 0.5% and from 6.0 to 15.7%, respectively. In contrast, the contribution of chemical weathering during winter time decreased from 82.7 ± 0.8 to 72.5 ± 0.3%, while anthropogenic contribution increased up to 22.2%. These results indicated that the water chemistry of the NR was mainly caused by a chemical weathering, followed by anthropogenic inputs and rainwater. This study will provide baseline information for comparing the water quality issue before and after the implementation of the Four Rivers Restoration Project of South Korea.     

Temperature as a tracer of hydrological dynamics in an anchialine cave system with a submarine spring

Hydrogeology Journal - Although temperature is a nonconservative tracer, it often provides useful information to understand hydrological processes. This study explores the potential of temperature...     

Multi-scale characterization of a complex karst and alluvial aquifer system in southern Germany using a combination of different tracer methods

Water suppliers face major challenges such as climate change and population growth. To prepare for the future, detailed knowledge of water resources is needed. In southern Germany, the state water supplier Zweckverband Landeswasserversorgung provides 3 million people with drinking water obtained from a complex karst and alluvial aquifer system and the river Danube. In this study, a combination of different tracing techniques was used with the goal of a multi-scale characterization of the aquifer system and to gain additional knowledge about groundwater flow toward the extraction wells in the Danube Valley. For the small-scale characterization, selected groundwater monitoring wells were examined using single-borehole dilution tests. With these tests, a wide range of flow behavior could be documented, including fast outflow within just a few hours in wells with good connection to the aquifer, but also durations of many weeks in low-permeability formations. Vertical flow, caused by multiple flow horizons or uprising groundwater, was detected in 40% of the tested wells. A regional multi-tracer test with three injections was used to investigate the aquifer on a large scale. For the highly karstified connection between a swallow hole and a spring group, high flow velocities of around 80 m/h could be documented. Exceptionally delayed arrivals, 250 and 307 days after the injection, respectively showing maximum velocities of 0.44 and 0.39 m/h, were observed in an area where low-permeability sediments overlay the karst conduits. With the chosen methods, a distinct heterogeneity caused by the geological setting could be documented on both scales.

     

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.