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1.
There are many factors affecting ungerground water chemistry of an oil-bearing sedimentary basin.The properties of underground water show variations in the vertical direction, giving rise to a vertical zonation with respect to underground water chemistry,Five zones could be divided downwards,including 1)The freshening zone due to meteoric water leaching (A):2)the evaporation-concentration zone near the surface(B);3) the freshening zone due to stratum compaction-released water(C1)-infiltration-concentration zone during the mudstone compaction and water releasing(C2);4) the freshening zone for clay mineral dehydration(D);and 5)the seepage-concentration zone(E).The hydrodynamic fields in the Songliao Basin are obviously asymmetrical,with the characteristics of gravity-induced centripetal flow recharged by meteoric water along the edge to the inner part of the basin mainly in its northern and eastern regions,centrifugal flow and crossformational flow in the center of the basin,as well as the cross-formation flow-evaporation discharge area in its southern area.Hydrodynamics controls the planar distribution of underground-water chemical fields;1)the freshening area due to penetrating meteoric water generally at the basin edges;2)the freshening area for mudstone compaction-released water at the center of the basin;3) the cross-formational area as the transitional aqrea;and 4)the concentration area by cross-formational flow and evaporation.The mineralization degree and the concentrations of Na^ and Cl^- and their salinity coefficeents tend to increase,while the concentrations of(CO3^2- HCO3^-) and SO4^2- and the metamorphism and desulfuration coefficients tend to decrease along the centrifugal flow direction caused by mudstone compaction in the depression area.But all of them tend to increase along the gravity-induced centripetal flow direction.  相似文献   

2.
Preferential flow and solute transport are common processes in the unsaturated soil, in which distributions of soil water content and solute concentrations are often characterized as fractal patterns. An active region model (ARM) was recently proposed to describe the preferential flow and transport patterns. In this study, ARM governing equations were derived to model the preferential soil water flow and solute transport processes. To evaluate the ARM equations, dye infiltration experiments were conducted, in which distributions of soil water content and Cl− concentration were measured. Predicted results using the ARM and the mobile–immobile region model (MIM) were compared with the measured distributions of soil water content and Cl− concentration. Although both the ARM and the MIM are two-region models, they are fundamentally different in terms of treatments of the flow region. The models were evaluated based on the modeling efficiency (ME). The MIM provided relatively poor prediction results of the preferential flow and transport with negative ME values or positive ME values less than 0.4. On the contrary, predicted distributions of soil water content and Cl− concentration using the ARM agreed reasonably well with the experimental data, with ME values higher than 0.8. The results indicated that the ARM successfully captured the macroscopic behavior of preferential flow and solute transport in the unsaturated soil.  相似文献   

3.
Sulfate transport in a Coastal Plain confining unit, New Jersey, USA   总被引：1，自引：0，他引：1  
 A transient 1-D, two-pathway non-equilibrium deterministic advective dispersion model was used to examine the distribution of chloride (43–100 mg/L) and sulfate (57–894 mg/L) concentrations in the 35-m-thick section of the Lower confining unit, Atlantic Coastal Plain, New Jersey, USA. The model was used to constrain hypotheses about how pore-water chemistry changed over time. Explanations of the solute concentrations were explored by inverse and direct methods given a few known constraints, including concentrations of pore-water constituents from 12 core samples, reported simulated flow rates, and estimated hydrogeologic properties. The hypothesis that is best supported by the model results is that the distribution of chloride and sulfate concentrations in the confining unit reflect the history of the aquifer system since it was filled with seawater at the last eustatic high, about 84×103yr BP. The model simulates fresh-water flushing of the seawater-permeated silts at a steady upward pore-water flow velocity of 8.8×10–6 m/d, with a dispersion coefficient of 9.2×10–7 m2/d, a dimensionless partition expression for chloride, βCl=0.981, and a dimensionless exchange coefficient, ωCl=0.31×10–2. Sulfate concentrations were simulated over the flow path using flow and dispersion values calculated for chloride transport plus a retardation term. Parameters for sulfate transport include retardation coefficient=4.51, βSO4=0.994, and ωSO4=0.31×10–2. Sensitivity analysis indicates that the model is most sensitive to flow velocity, and that fresh-water flushing of the confining unit is best simulated by having seawater concentration levels at the inflow boundary of the confining unit exponentially decrease with a concentration half-life rate of 825 yr. Received, January 1997 / Revised, April 1998, October 1998, January 1999 / Accepted, January 1999  相似文献   

4.
Geochemical evolution of uraniferous soda lakes in Eastern Mongolia   总被引：1，自引：1，他引：0  
Extremely high concentrations of uranium (U) were discovered in shallow, groundwater-fed hyperalkaline soda lakes in Eastern Mongolia. A representative groundwater sample in this area is dilute and alkaline, pH = 7.9, with 10 mM TIC and 5 mM Cl−. In contrast, a representative lake water sample is pH ~ 10 with TIC and Cl− each more than 1,000 mM. Groundwater concentrations of U range from 0.03 to 0.43 μM L−1. Lake water U ranges from 0.24 to >62.5 μM, possibly the highest naturally occurring U concentrations ever reported in surface water. Strontium isotopes 87Sr/86Sr varied in groundwaters from 0.706192 to 0.709776 and in lakes 87Sr/86Sr varied from 0.708702 to 0.709432. High concentrations of U, Na, Cl−, and K correlate to radiogenic Sr in lake waters suggesting that U is sourced from local Cretaceous alkaline rhyolites. Uranium-rich groundwaters are concentrated by evaporation and U(VI) is chelated by CO3−2 to form the highly soluble UO2(CO3)3−4. Modeled evaporation of lakes suggests that a U-mineral phase is likely to precipitate during evaporation.  相似文献   

5.
Nitrate pollution of groundwater in Toyserkan,western Iran   总被引：5，自引：2，他引：3  
A total of 95 groundwater samples were collected from Toyserkan, western Iran to assess the chemical composition and nitrate (NO3 −) status of groundwater. The most prevalent water type is Ca–HCO3 followed by water types Ca–Mg–HCO3. In comparison with the World Health Organization (WHO) drinking water guideline of 50 mg l−1 for NO3 −, a total of nine wells (9.5%) showed higher concentrations. In 36% of samples (34) NO3 − concentration was low (<20 mg l−1), and in 53.7% of samples (51), in the range of 20–50 mg l−1. The samples were classified into four groups based on NO3 − and chloride (Cl−) concentrations. Of the samples, 40% were classified as group 4 and were relatively high in Cl− and NO3 − (Cl− > 47 mg l−1, NO3 − > 27 mg l−1). The high correlation between NO3 − and Cl− (r = 0.86, p < 0.01) is consistent with a manure source, resulting from the practice of adding salt to animal feed. Pollution of groundwaters appeared to be affected by the application of inorganic fertilizer at greater than agronomic rates, Cl-salt inputs, and irrigation practice.  相似文献   

6.
This paper analyses flow and transport of pesticides from the unsaturated zone to groundwater so as to predict concentration of those contaminants in the Fucino Plain’s groundwater, by site investigations and numerical simulations. Pesticides were detected in surface water (peaks of 13 μg L−1) and groundwater (peaks of 0.37 μg L−1). Modelling tools made it possible to identify that pattern of precipitation, organic matter content, and root thickness are the key factors involved in vertical seepage of pesticides. Numerical simulations indicated that a significant fraction of contaminants is leached from the most surficial soil layers through runoff, while only a secondary fraction is mobilised towards groundwater. Likelihood of contaminating deep groundwater is fairly low, whereas surface waters show higher susceptibility. Results of the proposed conceptual hydrogeological model show that pesticides are more likely to be entrained by mixing of stream water with shallow groundwater in periods of high water exploitation from shallow wells.  相似文献   

7.
Dissolved major ions and important heavy metals including total arsenic and iron were measured in groundwater from shallow (25–33 m) and deep (191–318 m) tube-wells in southeastern Bangladesh. These analyses are intended to help describe geochemical processes active in the aquifers and the source and release mechanism of arsenic in sediments for the Meghna Floodplain aquifer. The elevated Cl− and higher proportions of Na+ relative to Ca2+, Mg2+, and K+ in groundwater suggest the influence by a source of Na+ and Cl−. Use of chemical fertilizers may cause higher concentrations of NH4+ and PO43− in shallow well samples. In general, most ions are positively correlated with Cl−, with Na+ showing an especially strong correlation with Cl−, indicating that these ions are derived from the same source of saline waters. The relationship between Cl−/HCO3− ratios and Cl− also shows mixing of fresh groundwater and seawater. Concentrations of dissolved HCO3− reflect the degree of water–rock interaction in groundwater systems and integrated microbial degradation of organic matter. Mn and Fe-oxyhydroxides are prominent in the clayey subsurface sediment and well known to be strong adsorbents of heavy metals including arsenic. All five shallow well samples had high arsenic concentration that exceeded WHO recommended limit for drinking water. Very low concentrations of SO42− and NO3− and high concentrations of dissolved Fe and PO43− and NH4+ ions support the reducing condition of subsurface aquifer. Arsenic concentrations demonstrate negative co-relation with the concentrations of SO42− and NO3− but correlate weakly with Mo, Fe concentrations and positively with those of P, PO43− and NH4+ ions.  相似文献   

8.
Present study is an effort to distinguish between the contributions of natural weathering and anthropogenic inputs towards high salinity and nutrient concentrations in the groundwater of National Capital Territory (NCT) Delhi, India. Apart from the source identification, the aquifer of entire territory has been characterized and mapped on the basis of salinity in space and water suitability with its depth. Major element chemistry, conventional graphical plots and specific ionic ratio of Na+/Cl−, SO4 2−/Cl−, Mg2+/Ca2+ and Ca2+/(HCO3 − + SO4 2−) are conjointly used to distinguish different salinization sources. Results suggest that leaching from the various unlined landfill sites and drains is the prime cause of NO3 − contamination while study area is highly affected with inland salinity which is geogenic in origin. The seasonal water level fluctuation and rising water level increases nutrients concentration in groundwater. Mixing with old saline sub-surface groundwater and dissolution of surface salts in the salt affected soil areas were identified as the principle processes controlling groundwater salinity through comparison of ionic ratio. Only minor increase of salinity is the result of evaporation effect and pollution inflows. The entire territory has characterized into four groups as fresh, freshening, near freshening and saline with respect to salinity in groundwater. The salinity mapping suggests that in general, for drinking needs, groundwater in the fresh, freshening and near freshening zone is suitable up to a depth of 45, 20 and 12 m, respectively, while the saline zones are unsuitable for any domestic use. In the consideration of increasing demand of drinking water in the area; present study is vital and recommends further isotopic investigations and highlights the need of immediate management action for landfill sites and unlined drains.  相似文献   

9.
This study presents the data on the hydrochemical characteristics and isotope chemistry of Liwa aquifer, which could be useful to clarify the hydrochemical facies and hydrogeological regime in the study area. Electric conductivity and total dissolved solid values show that the investigated water is slightly brackish, due to the effect of evaporation and the occurrences of evaporite rocks in the adjacent Sabkhas of Abu Dhabi. Major cations and anions arranged according to their decreasing concentrations are: Na+ > Ca+2 > K+ > Mg+2 and Cl− > HCO3 − > SO4−2, respectively. As sodium is the dominate cation and chloride is the prevailing anion, hydrochemically the groundwater of Liwa can be classified as Na–Cl rich, predominantly chloridic. Ion concentrations increase towards the northeast and presumably coincide with the lithological sources of ions. Factors affecting the hydrochemistry of the groundwater of the investigated area include the effect of weathering of soil and rocks, evaporation and agricultural activities. Stable isotopes of oxygen and hydrogen show that the shallow aquifers contain a single water type that originated in a distinct climatic regime. This water type deviates from the local meteoric water line, as well as from the Eastern Mediterranean Meteoric Water Line, suggesting potential evaporation of recharged water prior to infiltration. The waters are poor in tritium, and thus can be considered generally as indication for recharge prior to 1952. The degradation of groundwater quality can be attributed to evaporation and agricultural practices in most cases.  相似文献   

10.
Water samples collected from dug wells and tube wells from the Kurunegala District of Sri Lanka have been studied for their major hydrogeochemical parameters to understand the chemical quality of water in the terrain. The region is composed of Precambrian metamorphic rocks where groundwater is only available in the regolith and along weak structural discontinuities. The study of the major chemical constituents of groundwater revealed several relationships with the aquifer lithology. Groundwater from mafic rocks have high dissolved solids, while quartzose metaclastic rocks yield water with low dissolved solids. The study area displays very low SO4 2− contents of the groundwater. The chloride content is higher in the dry regions and in terrains underlain by pink granite and marble/calc gneiss while areas with marble, as expected, show high concentrations of Ca and Mg ions. The waters in the region can be classified into non-dominant cations to Na + K dominant and Cl− and HCO3 − dominant types. Water from charnockite-bearing areas tends to have non-dominant cations and more CO3 2− + HCO3 − types. Effects such as soluble salts in the regolith, fracture intensity and climatic variations play a significant role in the behavior of the hydrogeochemistry in the area.  相似文献   

11.
A one-dimensional mathematical model based on convection–dispersion equation in unsaturated porous media is presented to compute inorganic total solid concentration in the soil column under the Shiraz landfill. In addition, a dynamic mathematical model is formulated to simulate concentrations of ions such as Ca2+ , Mg2+, Fe2+, K+, Na+, Cl−, SO4 2− and HCO3 − as well as PH and EC in soil profile under the Shiraz landfill. Leachw model was applied to simulate water flow, water content and hydraulic conductivity in soil depth. The model was calibrated and verified by using different sets of data collected from several segments of soil depth in the study area. The numerical solution obtained using finite element method. The simulated values for the parameters were compared with measured values as well as analytical solution. The simulated results are in good agreement with measured values. This model could be applied to field scale problems for the landfill management.  相似文献   

12.
The hydrogeochemical study of surface and subsurface water of Mahi River basin was undertaken to assess the major ion chemistry, solute acquisition processes and water quality in relation to domestic and irrigation uses. The analytical results show the mildly acidic to alkaline nature of water and dominance of Na+ and Ca2+ in cationic and HCO3 − and Cl− in anionic composition. In general, alkaline-earth elements (Ca2+ + Mg2+) exceed alkalis (Na+ + K+) and weak acids (HCO3 −) dominate over strong acids (SO4 2+ + Cl−) in majority of the surface and groundwater samples. Ca2+–Mg2+–HCO3 − is the dominant hydrochemical facies both in surface and groundwater of the area. The weathering of rock-forming minerals mainly controlled the solute acquisition process with secondary contribution from marine and anthropogenic sources. The higher concentration of sodium and dissolved silica, high equivalent ratios of (Na+ + K+/TZ+), (Na+ + K+/Cl−) and low ratio of (Ca2+ + Mg2+)/(Na+ + K+) suggest that the chemical composition of the water is largely controlled by silicate weathering with limited contribution from carbonate weathering and marine and anthropogenic sources. Kaolinite is the possible mineral that is in equilibrium with the water, implying that the chemistry of river water favors kaolinite formation. Assessment of water samples for drinking purposes suggests that the majority of the water samples are suitable for drinking. At some sites concentrations of TDS, TH, F−, NO3 − and Fe are exceeding the desirable limit of drinking. However, these parameters are well within the maximum permissible limit except for some cases. To assess the suitability for irrigation, parameters like SAR, RSC and %Na were calculated. In general, both surface and groundwater is of good to suitable category for irrigation uses except at some sites where high values of salinity, %Na and RSC restrict its uses.  相似文献   

13.
This study assessed the levels of selected inorganic contaminants in streams and stream sediments in the effluent areas relating to the pyrometallurgical and hydrometallurgical treatment of gold ores in the Obuasi gold mine, Ghana. Water and stream sediment samples were taken from specific locations during the consecutive rainy and dry seasons, and concentrations of phosphate (PO4 3−), nitrate (NO3 −), chloride (Cl−), sulphate (SO4 2−), sodium (Na+), potassium (K+), calcium (Ca2+), magnesium (Mg2+), arsenic (As), copper (Cu), iron (Fe), zinc (Zn) and lead (Pb), were determined. Alkalinity, pH, temperature and specific electrical conductivity were also measured. In the water samples, the average pH range for both the seasons is 6.9–7.4, most anions and metals have relatively higher concentrations in the wet season than in the dry season at both the metallurgical sites. Trace metals concentrations were comparatively low (<0.01–5.00 mg/l), higher in the dry season at the pyrometallurgical sites. Irrespective of seasons, SO4 2− (0.80–949.50 mg/l) and PO4 3− (<0.01–6.30 mg/l) were pronounced at the pyrometallurgical sites, while NO3 − (0.01–98.45 mg/l) and Cl− (1.88-49.05 mg/l) were higher at the hydrometallurgical sites. In water samples, Ca2+ and SO4 2+ were the dominant cation and anion, respectively. In the stream sediments, except pH, NO3 −, Cl−, Na+ and Mg2+, all other parameter values were relatively higher at the hydrometallurgical areas. The average concentrations of Ca2+, Mg2+, As and Fe are remarkably high at both metallurgical sites (3,217–46,026 mg/kg). Overall, the level of parameters in the water samples are pronounced at pyrometallurgical sites, whereas the levels in sediments are higher at the hydrometallurgical sites.  相似文献   

14.
About 24 samples from hand-dug wells and boreholes were used to characterize concentrations of the main inorganic ions in a laterite environment under semi-arid climatic conditions in Tikaré, northern Burkina Faso. It was found that the most represented groundwater anion in groundwater was HCO3 − with average levels of 49.1 mg/L in the dry season and 33.5 mg/L in the rainy season. The most represented cation was Ca2+ with mean concentrations of 13.7 and 9.5 mg/L, respectively. The main processes, which influence the concentrations of these ions, are evaporation (dry season), local enrichment of recharge water in some elements, ion exchange and fixation by clay minerals (in case of K+). The best correlations were found between Ca2+ and Mg2+ (r = 0.95), Cl− and Na+ (r = 0.95), HCO3 − and Mg2+ (r = 0.89), HCO3 − and Ca2+ (r = 0.89), and between HCO3 − and Na+ (r = 0.80). In general, the quality of the groundwater from the different wells sampled for this study was good enough to serve as drinking water. However, there were situations where the quality of water was polluted because of anthropogenic contaminants (mainly NO3 −, K+, Cl−) from septic tanks and manure pits located in the vicinity of some sampled wells. In addition, application of fertilizers also represents a potential anthropogenic contamination source with regard to SO4 2−, Ca2+, K+, Na+, and Mg2+. Considering the high concentrations of SO4 2−, Mg2+, Na+ and Ca2+ found in one borehole, the deeper, fractured aquifers were also likely to be enriched in these elements. In contrast, the shallow aquifers are likely to be contaminated with Cl−, NO3 − and K+. Cl− and K+ seem to be locally present in recharge water as shown by their relative higher mean concentrations in the rainy season samples.  相似文献   

15.
Wadi El-Natrun area has recently undergone extensive urban and agricultural expansion. Due to the absence of natural surface irrigation supplies, the only source of water in the area is the Pliocene groundwater aquifer. As a result, secondary salinization from increased abstractions is the major threat to the groundwater aquifer. There is a dire need for efficient strategies to ensure long-term sustainability of the area’s productive agriculture. These strategies should be based on scientific spatio-temporal monitoring and analysis of the groundwater conditions that is also lacking. To capture the spatio-temporal variability in groundwater conditions, field measurements of total dissolved solids, electrical conductivity, pH, temperature, and water level as well as lab-based ionic composition were performed on 47 groundwater samples collected during 2006 and 2007. Determinations of the hydrochemical characteristics, water types, salt assemblages, and the sodium adsorption ratio were carried out on the samples. Reference data sets recorded in 1973 and 1997 were available for the area and were used to monitor the changes occurred in these periods. Geographic information system (GIS) was appraised for mapping and for integrated analysis of the different layers. Remotely sensed change detection techniques were applied to the Landsat TM and the ETM + imageries and used to highlight the extensive reclamation and urbanization and to find key trends for the alterations in the groundwater conditions and their spatial association with land covers. Results revealed a topographic depression-induced flow pattern, predominance of leaching and dissolution processes, the presence of saline lakes, over-pumping from the Pliocene aquifer, and temporal changes in land uses are the main factors combined to control the spatio-temporal variability in the groundwater. Results also clarified the presence of two: northwestern and southeastern zones that varied distinctively in their hydrodynamic and hydrochemical characteristics. The northwestern zone showed an average water level decline of 15 m, the water of which is brackish (av. 2,037 mg/l) with dominant Na+, Cl− and SO4 2− ions. The groundwater of this zone is characterized by high to very high salinity hazard and high to very high alkali hazard and is not recommended for irrigation on soils with poor drainage and without proper management for salinity control. The southeastern zone showed water level decline less than 2 m, the water of which is fresh (av. 424 mg/l) with major Na+, HCO3 −, Cl−, and SO4 2− ions, and quality suitable for irrigation with medium to high salinity and low to medium alkali hazards. The article represents the first step towards an integrated management of Wadi El-Natrun groundwater resources within a GIS framework.  相似文献   

16.
In this study, 92 groundwater samples were collected from the Attica region (Greece). Moreover, geographical information system database, geochemistry of groundwater samples and statistics were applied. These were used for studying the chemical parameters (NO3 −, Mg2+, Ca2+, Cl−, and Na+) and conductivity spatial distribution and for assessing their environmental impact. The ranges of chemical parameters of the water samples (in mg L−1) are: NO3 − 1–306, Mg2+ 2–293, Ca2+ 3–453, Cl− 5–1,988, and Na+ 4–475. The elevated concentrations of sodium, Mg2+, Cl− are attributed to natural contamination (seawater intrusion). On the other hand, NO3 − elevated concentrations are attributed to anthropogenic contamination (nitrate fertilizers). The results of the GIS analysis showed that elevated values of Na+, Mg2+, Cl− are related to shrubby and sparsely vegetated areas, while elevated values of NO3 − are connected with urban and agricultural areas.  相似文献   

17.
The aim of this study was to determine geochemical properties of groundwater and thermal water in the Misli Basin and to assess thermal water intrusion into shallow groundwater due to over-extraction. According to isotope and hydrochemical analyses results, sampled waters can be divided into three groups: cold, thermal, and mixed waters. Only a few waters reach water–rock chemical equilibrium. Thermal waters in the area are characterized by Na+–Cl−–HCO3−, while the cold waters by CaHCO3 facies. On the basis of isotope results, thermal waters in the Misli basin are meteoric origin. In particular, δ18O and δ2H values of shallow groundwater vary from −10.2 to −12.2‰ and −71.2 to −82‰, while those of thermal waters range from −7.8 to −10.1‰ and from −67 to −74‰, respectively. The tritium values of shallow groundwater having short circulation as young waters coming from wells that range from 30 to 70 m in depth vary from 10 to 14 TU. The average tritium activity of groundwater in depths more than 100 m is 1.59 ± 1.16, which indicates long circulation. The rapid infiltration of the precipitation, the recycling of the evaporated irrigation water, the influence of thermal fluids and the heterogeneity of the aquifer make it difficult to determine groundwater quality changes in the Misli Basin. Obtained results show that further lowering of the groundwater table by over-consumption will cause further intrusion of thermal water which resulted in high mineral content into the fresh groundwater aquifer. Because of this phenomenon, the concentrations of some chemical components which impairs water quality in terms of irrigation purposes in shallow groundwaters, such as Na+, B, and Cl−, are highy probably expected to increase in time.  相似文献   

18.
A study of environmental chloride, deuterium, oxygen-18, and tritium in deep sand profiles (35 m) has been carried out in order to estimate their relative value for measuring average groundwater recharge. The investigation was located at a 0.1-km2 site in Quaternary sands near the northwestern coast of Senegal in a zone of rainfed agriculture. By using a steady-state model for duplicate unsaturated zone chloride profiles, the long-term average recharge at the site was estimated to be 30 mm yr–1 or around 10% of the average precipitation (290 mm). The chloride concentration of adjacent shallow groundwater was relatively uniform and comparable to the unsaturated zone average, while the spatial variability in the depth distribution of Cl– in the unsaturated zone was considerable. Stable isotope (deuterium and oxygen-18) data show that there is some isotopic enrichment due to direct evaporation through the soil surface. The degree of heavy isotope enrichment is proportional to the extent of evaporative loss and there is good correspondance with the chloride enrichment. Nevertheless, stable isotopes cannot be used quantitatively to estimate the recharge. The excellent preservation of the peak in thermonuclear tritium in precipitation in the unsaturated zone at depths between 12 and 20 m enables an estimated annual recharge of 24 mm yr–1 in this area to be calculated, using the piston flow model. Agreement therefore between Cl and3H as tools for recharge measurement is reasonable over the site.  相似文献   

19.
Gas hydrate is a recently-found new source of energy that mostly exists in marine sediments. In recent years, we have conducted gas hydrate exploration in the South China Sea. The Xisha trough, one of the promising target areas for gas hydrate, is located in the northern margin of the South China Sea, adjacent to several large oil and gas fields. The Xisha trough extends 420 km long with the water depth of 1 500 m in the west part and 3 400 m in the east part and deposits thick sediments with organic matter content of 0.41%–1.02%. Previous studies on topographical features, geological P-T conditions, structural geology, sedimentary geology and geophysical bottom simulating reflectors (BSR) in the Xisha trough suggest that this area is favorable for the formation and accumulation of gas hydrate. In this paper, we present geochemical analyses for the sediment and pore water from a piston core at Site XS-01 in the Xisha trough. Seven pore water samples were analyzed for their anion (Cl−, SO4 2−, Br−, I−) contents, cation (Na, K, Ca, Mg) contents and trace element (Li, B, Sr, Ba, Rb, Mn) contents. Eight sediment samples were analyzed for stable carbon and oxygen isotopic compositions. A number of geochemical anomalies such as anions (e.g. Cl−, SO4 2−), cations (e.g. Ca, Mg) and trace elements (e.g. Sr, Ba, B) were found in this study. For example, the concentrations of Cl− and SO4 2− in pore water show a decreasing trend with depth. The estimated sulfate/methane interface (SMI) is only 18 m, which is quite similar to the SMI value of 23 m in the ODP164 Leg 997 at Blake Ridge. The Ca, Mg and Sr concentrations of pore water also decrease with depth, but concentrations of Ba, and Mg/Ca and Sr/Ca ratios increase with depth. These geochemical anomalies are quite similar to those found in gas hydrate locations in the world such as the Blake Ridge and may be related to the formation and dissociation of gas hydrates. The salt exclusion effect during the gas hydrate formation will cause an increase in major ion concentrations in the pore waters that diffused upward such as Cl. The anaerobic methane oxidation (AMO) may lead to the change of SO4 2− and other cations such as Ca, Mg, Sr and Ba in pore water. Low δ 13C value of authigenic carbonates is a good indicator for gas hydrate occurrence. However, the bulk sediment samples we analyzed all show normal δ 13C values similar to biogenic marine carbonates, and this may also suggest that no gas hydrate-related authigenic carbonates exist or their amount is so small that they are not detectable by using this bulk analytical method. In conclusion, we suggest that the Site XS-01 in the Xisha trough of the northern margin of the South China Sea is a potential target for further gas hydrate exploration. Translated from Quaternary Sciences, 2006, 26(3): 442–448 [译自: 第四纪研究]  相似文献   

20.
Groundwater and surface water samples were collected to improve understanding of the Senegal River Lower Valley and Delta system, which is prone to salinization. Inorganic ion concentrations and environmental isotopes (18O, 2H and 3H) in groundwater, river, lake and precipitation were investigated to gain insight into the functioning of the system with regard to recharge sources and process, groundwater renewability, hydraulic interconnection and geochemical evolution. The geochemical characteristics of the system display mainly cation (Ca2+ and/or Na+) bicarbonated waters, which evolve to chloride water type; this occurs during groundwater flow in the less mineralized part of the aquifer. In contrast, saline intrusion and secondary brines together with halite dissolution are likely to contaminate the groundwater to Na–Cl type. Halite, gypsum and calcite dissolution determine the major ion (Na+, Cl−, Ca2+, Mg2+, SO4 2− and HCO3 −) chemistry, but other processes such as evaporation, salt deposition, ion exchange and reverse exchange reactions also control the groundwater chemistry. Both surface water and groundwater in the system show an evaporation effect, but high evaporated signatures in the groundwater may be due to direct evaporation from the ground, infiltration of evaporated water or enriched rainwater in this region. The stable isotopes also reveal two types of groundwater in this system, which geomorphologically are distributed in the sand dunes (depleted isotopes) and in the flood plain (enriched isotopes). Consideration of the 3H content reinforces this grouping and suggests two mechanisms of recharge: contribution of enriched surface water in recharging the flood plain groundwater and, in the sand dunes area where water table is at depth between 8 and 13 m, slow recharge process characterized the submodern to mixed water.  相似文献   

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