Mobilization of Heavy Metals in a Saline Confined Aquifer as a Consequence of Rainwater Injection: A Case Study in Southern Vietnam.

An artificial recharge test was performed in Ho Chi Minh City, Vietnam to see the geochemical response of a saline coastal plain aquifer to the injected rainwater. The results show that the rainwater injection can cause mobilization of heavy metals due to pyrite oxidation and this phenomenon can persist even after the full recovery of the injected water. In this study, a 30-m-deep well was installed in a confined aquifer. Pyrite framboids were observed in the sediment samples collected during the well drilling. A total of 400 L rainwater was injected into the well for 70 min. After waiting 63 h, the well was extracted at a pump speed of 2.7 L/min and the chemistry of the pumped groundwater was monitored for 10 h. The groundwater showed geochemical features close to rainwater at the early stage of pumping and gradually changed to those of the background waters, especially, in electrical conductivity and Cl- concentration, as the pumping proceeded. However, the groundwater pumped in the later stage showed much increased concentrations in SO42-, total iron (FeT), AsT, Ni, Mn and Zn relative to the calculated mixing concentrations due to pyrite oxidation even though NO3-, the pyrite oxidant, already had disappeared. It was revealed from the geochemical modeling that the persistent pyrite oxidation was the result of the reaction with ferrihydrite, which precipitated in pores of the sediment by the injection of aerated water. We believe our study is a good example showing the importance of careful design of the artificial recharge systems to avoid or minimize the geochemical disturbance of aquifer.

Contribution of nitrate-nitrogen concentration in groundwater to stream water in an agricultural head watershed.

This study characterized nitrate-nitrogen (NO3-N) concentrations in groundwater and stream water in an agricultural head watershed in South Korea and identified the pollution load of NO3-N as a result of the groundwater entering streams using field surveys, analyses of chemical constituents, and numerical modeling. The mean NO3-N concentration in groundwater was 7.373 mg/L, which is approximately 1.9 times higher than concentrations found in stream water. The groundwater and stream water samples belonged to the Ca-HCO3 type. The concentration of NO3-N in groundwater tended to increase in the lowland areas downstream. There was seasonal variations of NO3-N in both the groundwater and stream water samples, with increases in concentration during the dry season (January-April) and decreases during the wet season (June-October). The NO3-N load in stream water to that in groundwater (R) was higher during the wet season (September) than the dry season (March), with R distinctly increasing in upstream areas relative to downstream areas, indicating that during the wet season, a large amount of NO3-N is introduced into stream water from groundwater. By analyzing the relationship between groundwater and stream water and through NO3-N transport modeling, it was revealed that in the watershed, the nitrate-N load in stream water is greatly augmented by inputs from groundwater, particularly in the middle and downstream areas.

Concentration, Source, and Total Health Risks of Cadmium in Multiple Media in Densely Populated Areas, China.

Cadmium (Cd) is a non-essential and harmful element to humans. Cadmium contamination is a serious issue for human health, especially in densely populated agroecology areas. In this study, the investigation of an agroecology area was conducted to gain insight into the relationship between Cd in wheat and soil and then evaluate the Cd total risk for human health. The soil samples and their matching wheat samples, underground water samples, and atmospheric deposition (air) samples were collected from a wheat-growing area in an agroecology plain. The cadmium concentration in the four types of media, in order, was air > soil > wheat > water. The mean concentration of the geoaccumulation index (Igeo) showed that the total Cd in soil (Cd-T) and Cdair reached a mild and moderate pollution level. The results of the correlation and principal component analysis (PCA) showed that the majority of Cdwheat originated from Cd-2 (exchangeable), Cd-4 (humic acid-bound), and Cd-7 (residual). Furthermore, the results of the stepwise multiple linear regression (SMLR) showed that three fractions were primarily controlled by Cd-T: clay, cation exchange capacity (CeC), and total organic carbon (TOC). In addition, the total cancer risk (CR) of Cd in multiple media was, in the order wheat > water > soil > air. It is noteworthy that the Cd content in underground water and wheat by the ingestion pathway posed cancer risks to the local residents and provided a comprehensive insight into multiple media environment management. Furthermore, it provides a very significant basic study for detailed research into the mobility and transformation for factions.

Occurrence of metal-rich acidic groundwaters around the Mekong Delta (Vietnam): A phenomenon linked to well installation.

Acidic groundwaters enriched with heavy metals are frequently observed in the coastal plain aquifers. The acidic pHs are observed even in the deep confined aquifers in southern Vietnam. This study geochemically explores the causes of these acidic groundwaters by investigating 41 groundwater samples, 4 soil samples and a 54 m long sediment core and the long-term monitoring data (4189 observations) obtained from 178 wells of the National Groundwater Monitoring Network for the South of Vietnam (NGMNS). The groundwater data show elevated Fe, Mn, Al, Pb, and Zn concentrations as the pH becomes acidic and suggest pyrite oxidation be the major cause for the groundwater acidification. This is further confirmed by pyrite framboids observed in the sediment or soil samples taken from the sites where strongly acidic groundwaters were observed. Results of leaching experiments using sediment and soil samples indicate that high metal concentrations in the acidic pH are associated with the increased metal solubility and mineral dissolution kinetics. The acidification of deep groundwaters is revealed to be associated with well installation, indicating the importance of proper well-installation techniques to protect water quality of deep confined aquifers.

Inhibitory effect of veterinary antibiotics on denitrification in groundwater: a microcosm approach.

Veterinary antibiotics in groundwater may affect natural microbial denitrification process. A microcosm study was conducted to evaluate the influence of sulfamethazine and chlortetracycline at different concentrations (0, 0.01, 0.1, and 1.0 mg/L) on nitrate reduction in groundwater under denitrifying condition. Decrease in nitrate removal and nitrite production was observed with the antibiotics. Maximum inhibition of nitrate removal was observed after seven days of incubation with 0.01 mg/L sulfamethazine (17.0%) and 1.0 mg/L chlortetracycline (15.4%). The nitrite production was inhibited with 1.0 mg/L sulfamethazine to 82.0% and chlortetracycline to 31.1%. The initial/final nitrate concentrations indicated that 0.01 mg/L sulfamethazine and 1.0 mg/L chlortetracycline were most effective in inhibiting activity of denitrifying bacteria in groundwater. After 12 days of incubation, the sulfamethazine biodegradation was observed whereas chlortetracycline was persistent. Sulfamethazine and chlortetracycline in groundwater could inhibit the growth and capability of naturally occurring denitrifying bacteria, thereby threatening nitrate pollution in groundwater.

Current approaches for mitigating acid mine drainage.

AMD is one of the critical environmental problems that causes acidification and metal contamination of surface and ground water bodies when mine materials and/or over burden-containing metal sulfides are exposed to oxidizing conditions. The best option to limit AMD is early avoidance of sulfide oxidation. Several techniques are available to achieve this. In this paper, we review all of the major methods now used to limit sulfide oxidation. These fall into five categories: (1) physical barriers,(2) bacterial inhibition, (3) chemical passivation, ( 4) electrochemical, and (5) desulfurization.We describe the processes underlying each method by category and then address aspects relating to effectiveness, cost, and environmental impact. This paper may help researchers and environmental engineers to select suitable methods for addressing site-specific AMD problems.Irrespective of the mechanism by which each method works, all share one common feature, i.e., they delay or prevent oxidation. In addition, all have limitations.Physical barriers such as wet or dry cover have retarded sulfide oxidation in several studies; however, both wet and dry barriers exhibit only short-term effectiveness.Wet cover is suitable at specific sites where complete inundation is established, but this approach requires high maintenance costs. When employing dry cover, plastic liners are expensive and rarely used for large volumes of waste. Bactericides can suppress oxidation, but are only effective on fresh tailings and short-lived, and do not serve as a permanent solution to AMD. In addition, application of bactericides may be toxic to aquatic organisms.Encapsulation or passivation of sulfide surfaces (applying organic and/or inorganic coatings) is simple and effective in preventing AMD. Among inorganic coatings,silica is the most promising, stable, acid-resistant and long lasting, as compared to phosphate and other inorganic coatings. Permanganate passivation is also promising because it creates an inert coating on the sulfide surface, but the mechanism by which this method works is still unclear, especially the role of pH. Coatings of Fe-oxyhydroxide, which can be obtained from locally available fly ash are receiving attention because of its low cost, self-healing character, and high cementation capacity. Among organic coatings, lipids and natural compounds such as humic acid appear to be encouraging because they are effective, and have a low environmental impact and cost. Common advantages of organic vs. inorganic coatings are that they work best at low pH and can prevent both chemical and biological oxidation.However, organic coatings are more expensive than inorganic coatings. Furthermore,while organic coatings are effective under laboratory conditions, they often fail under field conditions or require large amounts of reagents to insure effectiveness.Electrochemical cover technology may become a suitable technique to prevent AMD, but the mechanism by which this technique operates is still under investigation.Limitations of this method include the initial capital cost and ongoing costs of anodes and cathodes.Desulfurization is an alternative process for managing large-scale sulfide wastes/tailings. This process can separate sulfide minerals into a low-volume stream, leaving mainly waste with low sulfur content that will be non-acid-generating. The attractiveness of desulfurization is that it is simple and economic.Our review has clearly disclosed that more information is needed for most of the AMD-mitigation techniques available. Silica passivation has shown promise, butmore extensive field-testing is needed to reduce it to commercial viability. Silica is the dominant element in fly ash, and therefore, its use as a low-cost, easily accessible coating should be evaluated. Permanganate passivation also requires further study to understand the role of pH. The secondary formation of Fe-oxyhydroxide minerals from Fe-oxyhydroxides, from the standpoint of their phase transformation,stability and effectiveness, should be assessed over longer experimental periods. All inorganic coatings are designed to inhibit abiotic oxidation of pyrite; however, their effect on biotic pyrite oxidation is not well known and should be further studied.Currently, there is no information available on longer-term field application of organic reagents. Such information is needed to evaluate their lifetime environmental and performance effects. Future studies require spectroscopic analyses of all coating types to achieve a better understanding of their surface chemistry. In addition,a thorough mineralogical and geochemical characterization of waste materialsis essential to understand the acid generating potential, which can indeed help to select better prevention measures.From having performed this review, we have concluded that no single method is technologically mature, although the majority of methods employed are promising for some applications, or at specific sites. Combining techniques can help ac~Ie:eAMD containment in some cases. For example, applying dry cover (e.g., sml) mcombination with liming material or a bactericide, or applying inorganic coatings(e.g., silica) along with organic reagents (e.g., lipids or humic acid) may be moreeffective than utilizing any single technique alone.

Molecular analysis of spatial variation of iron-reducing bacteria in riverine alluvial aquifers of the Mankyeong River.

Alluvial aquifers are one of the mainwater resources in many countries. Iron reduction in alluvial aquifers is often a major anaerobic process involved in bioremediation or causing problems, including the release of As trapped in Fe(III) oxide. We investigated the distribution of potential iron-reducing bacteria (IRB) in riverine alluvial aquifers (B1, B3, and B6 sites) at the Mankyeong River, Republic of Korea. Inactive iron reduction zones, the diversity and abundance of IRB can be examined using a clone library and quantitative PCR analysis of 16S rRNA genes. Geobacter spp. are potential IRB in the iron-reducing zone at the B6 (9 m) site, where high Fe(II) and arsenic (As) concentrations were observed. At the B3 (16 m) site, where low iron reduction activity was predicted, a dominant clone (10.6%) was 99% identical in 16S rRNA gene sequence with Rhodoferax ferrireducens. Although a major clone belonging to Clostridium spp. was found, possible IRB candidates could not be unambiguously determined at the B1 (18 m) site. Acanonical correspondence analysis demonstrated that, among potential IRB, only the Geobacteraceae were well correlated with Fe(II) and As concentrations. Our results indicate high environmental heterogeneity, and thus high spatial variability, in thedistribution of potential IRB in the riverine alluvial aquifersnear the Mankyeong River.

Co-contamination of arsenic and fluoride in the groundwater of unconsolidated aquifers under reducing environments.

The co-contamination of arsenic (As) and fluoride (F(-)) in shallow aquifers is frequently observed worldwide, and the correlations between those contaminants are different according to the redox conditions. This study geochemically explores the reasons for the co-contamination and for the redox-dependent correlations by investigating the groundwater of an alluvial aquifer in Korea. Geochemical signatures of the groundwater in the study area show that the As concentrations are enriched by the reductive dissolution of Fe-(hydr)oxides, and the correlations between As and F(-) concentrations are poor comparatively to those observed in the oxidizing aquifers. However, F(-) concentrations are strongly dependent on pH. Desorption/adsorption experiments using raw soils and citrate-bicarbonate-dithionite treated soils indicated that Fe-(hydr)oxides are the important As and F(-) hosts causing the co-contamination phenomenon. The weaker correlation between F(-) and As in reducing aquifers is likely to be associated with sulfate reduction, which removes As from groundwater without changing the F(-) concentration.

Relations of As concentrations among groundwater, soil, and bedrock in Chungnam, Korea: implications for As mobilization in groundwater according to the As-hosting mineral change.

Arsenic (As) concentrations and As-bearing minerals in bedrock and soil, and their relations with groundwater concentrations were investigated in a small agricultural area of Korea. The As concentration of the bedrock shows a wide variation (<0.5-3990 mg/kg) and is well correlated with that in the contacting groundwaters (23-178 µg/L). Soils, the weathering product of bedrock, show the lower and more dispersed As concentrations (8.8-387 mg/kg) than the bedrock. But the soil As concentrations are very high relative to those reported from other areas. The As concentrations in the shallow groundwaters are comparatively low (<20 µg/L) and are independent of the soil concentration. Arsenopyrite is the major As-bearing mineral in the bedrock and its oxidation controls the As levels in deep groundwater. In contrast, As mostly resides in soil as Fe-(hydr)oxide-bound forms. Due to low pH and oxidizing redox condition, the release of As from Fe-(hydr)oxides is largely suppressed, and the shallow groundwater shows low As concentrations generally satisfying the drinking water limit. However, it is suggested that the disturbance of soil geochemical conditions by land use changes would cause a serious As contamination of the shallow groundwaters.

Processes controlling the variations of pH, alkalinity, and CO2 partial pressure in the porewater of coal ash disposal site.

Alkalinity, pH, and pCO2 are generally regarded as the most important parameters affecting trace element leaching from coal ashes. However, little is known about how those parameters are actually regulated in the field condition. This study investigated the processes controlling those parameters by observing undisturbed porewater chemistry in a closed ash disposal site. The site is now covered with 30-50 cm thick soils according to the management scheme suggested by the Waste Management Law of Korea and our results show the important role of soil cover regulating those parameters in the shallow porewater. Without the soil cover, the shallow porewater shows low pCO2 and alkalinity, and highly alkaline pH. In contrast, the porewater shows much higher alkalinity and near neutral pH range when the site was covered with the low permeability soils. This difference was caused by the CO2 supply condition changes associated with the changes in infiltration rate. The geochemical modeling shows that the calcite precipitations induced by porewater aging, dolomitization, and weathering of solid phases are the main processes controlling alkalinity, pH, and pCO2 in the deep saline porewaters. The weathering of coal ash plays the most important role decreasing the alkalinity in the deep porewater.

Tracing the geographical origin of beefs being circulated in Korean markets based on stable isotopes.

We have examined the carbon, nitrogen and oxygen isotopic compositions of American, Mexican, Australian, New Zealand and Korean beefs, which are currently being circulated in Korean markets, to check whether stable isotope ratios can identify their country of origin. Each beef exhibited statistically distinct isotopic compositions, especially in oxygen and carbon, because of the different isotopic compositions of their water and cattle feeds. Nevertheless, their isotopic compositions still showed some overlap, especially among USA, Australian, and Korean beefs, which sometimes resulted in significant misidentification when a single isotope was considered. However, the discrimination was generally successful when both the carbon and the oxygen isotopes were used.

Arsenic concentration in porewater of an alkaline coal ash disposal site: Roles of siderite precipitation/dissolution and soil cover.

The geochemical behavior of As in porewaters of an alkaline coal ash disposal site was investigated using multilevel samplers. The disposal site was in operation from 1983 until 1994 and was covered with 0.3-0.5m thick soils in 2001 when this study was initiated. Sequential extraction analyses and batch leaching experiments were also performed using the coal ash samples collected from the disposal site. The results suggest the important roles of siderite (FeCO(3)) precipitation/dissolution and soil cover, which have been ignored previously. Arsenic levels in the porewater were very low (average of 10microgL(-1)) when the site was covered with soil due to coprecipitation with siderite. The soil cover enabled the creation of anoxic conditions, which raised the Fe concentration by the reductive dissolution of Fe-(hydr)oxides. Because of the high alkalinity generated from the alkaline coal ash, even a small increase in the Fe concentration (0.66mgL(-1) on average) could cause siderite precipitation. When the soil cover was removed, however, an oxidizing condition was created and triggered the precipitation of dissolved Fe as (hydr)oxides. As a result, the dissolution of previously precipitated As-rich siderite caused higher As concentration in the porewater (average of 345microgL(-1)).

Importance of surface geologic condition in regulating As concentration of groundwater in the alluvial plain.

The arsenic (As) concentrations in the groundwater of alluvial plains generally show high spatial variability. We geochemically explore the factors causing the spatial variability in an alluvial plain that is mainly used for rice cultivation, the commonest land-use pattern in alluvial plains of Asia. We investigate the chemical processes, sources of chemicals that affect the behavior of As, and their relationships with the geologic conditions at seven multilevel sampler sites. All sites showed As concentrations that increased with depth at shallow levels and decreased at greater depths, which is the typical vertical pattern in alluvial aquifers where Fe-(hydr)oxide reduction is the major As release mechanism. Data show that NO(3) and SO(4) originating from the land surface play important roles in suppressing the increase in As concentration by buffering the redox potential at shallow depths and by precipitating As with sulfide minerals at deep depths, respectively. The As concentration in the intermediate depth range was also low in the presence of SO(4), because its reduction can occur together with Fe-(hydr)oxide reduction in a wide range of redox potentials. As a result, the maximum As concentrations at the sites where the land was covered with a thick silt layer (approximately 5m) were 3- to 5-times higher than those at other sites due to the supply of NO(3) and SO(4) from land surface being largely limited by the silt layer. This indicates that the surface geology could be an important indicator for the As concentration in alluvial groundwater.

Hydrochemical and multivariate statistical interpretations of spatial controls of nitrate concentrations in a shallow alluvial aquifer around oxbow lakes (Osong area, central Korea).

Hydrochemical and multivariate statistical interpretations of 16 physicochemical parameters of 45 groundwater samples from a riverside alluvial aquifer underneath an agricultural area in Osong, central Korea, were performed in this study to understand the spatial controls of nitrate concentrations in terms of biogeochemical processes occurring near oxbow lakes within a fluvial plain. Nitrate concentrations in groundwater showed a large variability from 0.1 to 190.6 mg/L (mean=35.0 mg/L) with significantly lower values near oxbow lakes. The evaluation of hydrochemical data indicated that the groundwater chemistry (especially, degree of nitrate contamination) is mainly controlled by two competing processes: 1) agricultural contamination and 2) redox processes. In addition, results of factorial kriging, consisting of two steps (i.e., co-regionalization and factor analysis), reliably showed a spatial control of the concentrations of nitrate and other redox-sensitive species; in particular, significant denitrification was observed restrictedly near oxbow lakes. The results of this study indicate that sub-oxic conditions in an alluvial groundwater system are developed geologically and geochemically in and near oxbow lakes, which can effectively enhance the natural attenuation of nitrate before the groundwater discharges to nearby streams. This study also demonstrates the usefulness of multivariate statistical analysis in groundwater study as a supplementary tool for interpretation of complex hydrochemical data sets.

Tracing the sources of nitrate in the Han River watershed in Korea, using delta15N-NO3- and delta18O-NO3- values.

The dissolved nitrate concentrations and their nitrogen and oxygen isotopic ratios were analyzed in seasonal samples from Korea's Han River to ascertain the seasonal and spatial variations of dissolved nitrate and its possible sources. Nitrate concentrations in the South Han River (SHR) were much higher than those in the North Han River (NHR), probably because of the more extensive distribution of agricultural fields, residential areas and animal farms in the SHR drainage basin. The nitrogen isotopic composition of dissolved nitrate indicates that nitrate-nitrogen (NO(3)(-)-N) is derived mainly from atmospheric deposition and/or soil organic matter in the NHR but comes principally from manure or sewage, with only a minor contribution from atmospheric deposition or soil organic matter, in the SHR. The oxygen isotopic compositions of dissolved nitrate suggest that most atmospheric nitrate undergoes microbial nitrification before entering the river.

Comparison of microbial indicators under two water regimes in a soil amended with combined paper mill sludge and decomposed cow manure.

An incubation study was conducted under laboratory conditions to compare the effects of soil amendment of combined paper mill sludge (PS) and decomposed cow manure (DCM) on selected microbial indicators. A lateritic soil (Typic Haplustalf) was amended with 0 (control), 20 or 80tha(-1) (wet weight) of PS or DCM. The amended soils were then adjusted to 60% water holding capacity (WHC) or submerged conditions, and incubated at 27 degrees C in dark for up to 120days (d). The microbial biomass C (MBC), the basal soil respiration and the enzyme activities of the beta-glucosidase, acid phosphatase and sulphatase were analyzed at day 15, 30, 45, 60 and 120. Compared to the unamended soil (control), the MBC, the basal soil respiration and the enzyme activities increased with the rate of PS and DCM. At similar rate, the DCM treatment increased significantly the MBC, the soil respiration and the enzyme activities compared to the PS treatment. Also, the water regimes affected the microbial activities. At 60% WHC, the MBC and soil respiration increased during the first 30d and decreased thereafter. The enzyme activities showed similar trends, where they increased for the first 60d, and decreased thereafter. In contrast, under submerged condition, the MBC and enzymes activities declined during 120d, whereas the soil respiration increased. Compared to the control, the used of PS and DCM had no negative impact of the soil microbial parameters, even at the highest application rate. Long-term field experiments are required to confirm these laboratory results.

Arsenic fractions and enzyme activities in arsenic-contaminated soils by groundwater irrigation in West Bengal.

A study for the effect of arsenic (As) contamination on beta-glucosidase, urease, acid-/alkaline-phosphatase, and arylsulphatase activities was conducted in As contaminated soils of West Bengal, India. The studied soils show low total As contents relative to those in other As-contaminated sites. A sequential extraction technique was used to quantify water soluble, exchangeable, carbonate bound, Fe/Mn oxide bound, organic bound, and residual As fractions. Arsenic concentrations in the two most labile fractions (i.e., water soluble and exchangeable fractions) were generally low. The studied enzymes were significantly and negatively correlated with water soluble and exchangeable As forms but did not show any significant correlations with other forms, indicating that water soluble and exchangeable forms exert a strong inhibitory effect on the soil enzyme activities. It is thus suggested that the enzyme activity can be helpful in assessing the effects of As on biochemical quality of soils.

The accumulation of radiocesium in coarse marine sediment: effects of mineralogy and organic matter.

The controlling factors affecting the accumulation of (137)Cs in marine sediment have not been investigated in detail, especially in coarse grained sediment. Eighty eight coarse marine sediment samples near Wuljin, Korea, were characterized by quantitative X-ray-diffraction (XRD), gamma-ray, and total organic carbon (TOC) analysis. Those factors were then compared. The grain size was in the range of -0.48 to 3.6Mdphi corresponding to sand grains. TOC content was in the range of 0.06-1.75%, and the concentration of (137)Cs was

Fluorine geochemistry in bedrock groundwater of South Korea.

High fluoride concentrations (median=4.4 mg/L) in deep bedrock groundwater of South Korea prevent the usage of it as a drinking water source. The hydrogeochemistry of deep thermal groundwaters (N=377) in diverse bedrocks has been studied in order to evaluate the geologic and geochemical controls on fluoride concentrations in groundwater. The groundwater samples were clustered geologically, and the average and median concentrations of fluoride were compared by the Mann-Whitney U test. The order of median fluoride concentration with respect to geology is as follows: metamorphic rocks> or =granitoids > or =complex rock>>volcanic rocks> or =sedimentary rocks. This result indicates that the geological source of fluoride in groundwater is related to the mineral composition of metamorphic rocks and granitoids. With respect to groundwater chemistry, the fluoride concentration was highest in Na-HCO3 type groundwater and lowest in Ca-HCO3 type groundwater. Ionic relationships also imply that the geochemical behavior of fluoride in groundwater is related to the geochemical process releasing Na and removing Ca ions. The thermodynamic relationship between the activities of Ca and F indicates that fluoride concentration is controlled by the equilibrium of fluorite (CaF2). In other words, the upper limits of fluoride concentration are determined by the Ca ion; i.e., Ca concentrations play a crucial role in fluoride behavior in deep thermal groundwater. The result of this study suggests that the high fluoride in groundwater originates from geological sources and fluoride can be removed by fluorite precipitation when high Ca concentration is maintained. This provides a basis for a proper management plan to develop the deep thermal groundwater and for treatment of high fluoride groundwater frequently found in South Korea.

Radiocesium reaction with illite and organic matter in marine sediment.

The mineralogical effect on the (137)Cs reaction with marine sediment has not been systematically studied yet, even though illite has been known to adsorb Cs preferentially on its frayed edge sites in a low Cs concentration. Ninety-three marine sediment samples were collected near Yangnam, Korea for quantitative X-ray-diffraction (XRD), gamma-ray, and total organic carbon (TOC) analysis. Illite content was in the range of 0-23 wt.% and those of (137)Cs and TOC were minimum detectable activity (MDA) approximately 7.19 Bq/kg-dry and approximately 3.32%, respectively. The illite content in the marine sediment showed a good relationship with the (137)Cs content (R(2)=0.69), but with an increase in the illite content, the relationship became less linear. This trend can be clearly shown in two groups of samples with different size fractions (< and >5Mdvarphi). For the samples of larger particle sizes (low contents of illite), the relationship is linear, but for the samples of the smaller particle sizes (high illite content) it is less linear with a decreased slope, indicating that increase in illite content does not significantly contribute to the fixation of (137)Cs in marine sediment. Rather, the TOC has a more linear relationship with (137)Cs content with no slope change in all particle size ranges. This may indicate that humic materials in marine sediment block the access of (137)Cs to the frayed edge site and reduces the adsorption of (137)Cs on illite and that the organic materials in marine sediment play more important roles in adsorbing Cs than illite.