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1.
Major cations and anions were investigated in the Damietta branch of the River Nile. The branch is divided into two different regions; the fresh Nile water (Region A) and the mostly marine environment (Region B). The latter region represents the Damietta estuary. The relative abundance of the major ions in the fresh water system was Na > Ca > Mg > K, HCO3 > Cl > SO4 > CO3, while in the mostly marine area it was Na > Mg > K > Ca, Cl > HCO3 > SO4 > CO3. Regional and monthly variations of the major ions were related to the duration of the Nile discharge and climatic conditions. The major ions -to- chloride ratios for Region A were higher than those in the adjacent Mediterranean waters, while those for the mostly marine region were slightly lower.  相似文献   

2.
Reclaimed water is efficiently used to recover the dry river, but river water and groundwater may be impacted considering the water quality. Thus, it is critical to study the factors controlling water chemistry. Samples of reclaimed water, river and groundwater were collected monthly from January to September in 2010, in Huai River (North China). And samples were analyzed for major 15 physio-chemical parameters. Using hierarchical cluster analysis, 9 months are divided into two distinct groups, which show the clear temporal variation. In reclaimed water and river water, one group includes February, while the other includes other months. In shallow and deep groundwater, one group includes months from January to April, while the other encompasses others. Monitoring stations are classified into three groups. Group A with high value of ions and nitrogen (order: NH4-N > NO3-N > NO2-N) includes reclaimed water and river water. Group B with moderate concentration and nitrogen (order: NO3-N > NH4-N > NO2-N) includes all shallow groundwater and one deep groundwater. Group C with the low value and nitrogen (order: NO3-N > NO2-N > NH4-N), includes two deep groundwater. Using multivariate analysis and ionic relationships, river water chemistry is found to be controlled by reclaimed water and evaporation process; chemistry in shallow groundwater and one deep groundwater, with type of Na–Ca(Mg)–HCO3–Cl, is controlled by dissolution of calcite, carbonate weathering. Additionally, reactions of nitrification, denitrification and cation exchange occur in the infiltration of reclaimed water; chemistry in the other deep groundwater, with type of Ca–Mg–HCO3–Cl, is controlled by dissolution of calcite, carbonate weathering and denitrification.  相似文献   

3.
ABSTRACT

The regional groundwater groups of central Israel include:

  1. bicarbonate waters representing the replenishment areas;

  2. chloride waters representing the confined and the base-level zones;

  3. sulfate waters of the intermediate zones (fig. 2).

These water types were found to fit broadly into five hydrogeographical groups.

The chemical evolution of the ground waters is a function of: a) lithology and solubility of the aquifer components and of the surrounding strata; b) mixing between groundwater bodies of different composition. The first factor is important mainly within the confined zones while the latter is conspicuous in the Rift Valley and adjacent areas.

Groundwater mixing within the Dead Sea basin produces waters with Mg > Na > Ca, and Cl ? SO > HCO3. Other brines show the order: Ca > Na > Mg. All these brines show compositions different from ocean water.  相似文献   

4.
Chemical studies have been carried out on a number of water wells from the Dibdiba Formation northeast of Kuwait. Water salinity of this formation ranges between 3,300 mg/l to 7,000 mg/l, increasing with depth. The water entrapped in Dibdiba Formation is mainly sodium chloride type which can be differentiated into three different groups according to the ranges of concentration of the main cations and anions. These groups are: (3331113) sodium chloride water type in which Cl > Na, group (3333113) sodium chloride water type in which Na > Cl. In both groups the sequence of dominant cations is Na > Ca > Mg. Group (3333111) sodium chloride water type has Na > Cl and the sequence of dominant cations is Na > Mg > Ca. Chemical ratios of Ca/Mg, Na/Cl, and C1/HCO3 were worked out for Dibdiba ground water. The ratio of Ca/Mg Dibdiba Formation ranges from 0.4 to 8.58, the ratio of Na/Cl ranges between 0.98 to 1.33, and the ratio of C1/HCO3 is 232. A plot of chemical analysis on a trilinear diagram shows that Dibdiba Formation ground-water chemical properties are dominated by alkalies (Na > Ca) and strong acid (Cl > SO4). Water chemistry may reflect the history of the flow path, indicating regional flow as shown by increasing Na+, Cl-, SO–4 and where Ca+, Mg+ achieve equilibrium.  相似文献   

5.
ABSTRACT

Water quality in the arid regions has long been an issue of great concern in the world. In this study, quantitative research was carried out to create new knowledge to understand the processes that determine the variation in the groundwater chemical composition of the Yinchuan Plain, China. In this context, the distribution and zonation characteristics of groundwater in this area were assessed using geochemical modelling of groundwater quality evolution. The results show the existence of an obvious zonation from the recharge area to the discharge area in the study area. Dominant anions transform from HCO3 in the inclined pluvial area to HCO3·SO4·Cl in the discharge region, while the main cations vary from Ca and Mg to Na and Mg. The simulation results indicate that the evaporation process triggers 2–35% of groundwater loss, leading to an increase in the total dissolved solids. The irrigation leakage mixes with the groundwater at about 8:2, suggesting that the irrigation leakage dilutes the groundwater.  相似文献   

6.
Some 300 measurements under a wide range of flow conditions were used to construct regression models to predict concentrations of six major ions in a moorland stream draining intermediate-basic lavas in Scotland. Ca, Mg, and HCO3 were very closely related to discharge in log-log regressions (r2 > 90 percent). Na and Cl required inclusion of seasonal functions for best prediction (r2 = 76 per cent in both cases). K concentrations were predicted from discharge, direction of stage change, and a seasonal function. Annual losses of Ca, Mg, and HCO3 were 252, 36, and 871 kg ha ?1, substantially larger than those for upland catchments on acid rocks. Losses of K, Na, and Cl were of a similar order to other upland sites.  相似文献   

7.
This paper examines groundwater hydrochemical characteristics during mixing between thermal and non-thermal groundwater in low-to-medium temperature geothermal fields. A case study is made of Daying and Qicun geothermal fields in the Xinzhou basin of Shanxi province, China. The two geothermal fields have similar flow patterns, with recharge sourced from precipitation in mountain areas heated through a deep cycle, before flowing into overlying Quaternary porous aquifers via fractures. Hydrochemical features of 60 ground- and surface water samples were examined in the context of hydrogeologic information. The average temperatures of the deep geothermal reservoirs are estimated to be 125 °C in Daying field, and 159 °C in Qicun field, based on Na–K–Mg geothermometry, while slightly lower estimates are obtained using silica geothermometers. Hydrochemical features of thermal water are distinct from cold water. Thermal groundwater is mainly Cl·SO4–Na type, with high TDS, while non-thermal groundwater is mostly HCO3–Ca·Mg and HCO3–Ca type in the Daying and Qicun regions, respectively. Hydrogeochemical processes are characterized by analyzing ion ratios in various waters. Higher contents of some minor elements in thermal waters, such as F, Si, B and Sr, are probably derived from extended water–rock interaction, and these elements can be regarded as indicators of flow paths and residence times. Mixing ratios between cold and thermal waters were estimated with Cl, Na, and B concentrations, using a mass balance approach. Mixing between ascending thermal waters and overlying cold waters is extensive. The proportion of water in the Quaternary aquifer derived from a deep thermal source is lower in Daying geothermal field than in Qicun field (5.3–7.3% vs. 6.3–49.3%). Mixing between thermal and non-thermal groundwater has been accelerated by groundwater exploitation practices and is enhanced near faults. Shallow groundwater composition has also been affected by irrigation with low-temperature thermal water.  相似文献   

8.
Mineral and thermal water chemistry from the Azores archipelago was investigated in order to discriminate among hydrochemical facies and isotopic groups and identify the major geochemical processes that affect water composition. A systematic geochemical survey of mineral and thermal water chemistry was carried out, incorporating new data as well as results from the literature. The Azores are a volcanic archipelago consisting of nine islands and samples were collected at São Miguel, Graciosa, Faial, São Jorge, Pico and Flores islands. Hydrothermal manifestations show the effects of active volcanism on several islands. Discharges are mainly related to active Quaternary central volcanoes, of basaltic to trachytic composition, but also some springs are related to older dormant or extinct volcanoes.Multivariate analysis – principal component and cluster analysis – enables classification of water compositions into 4 groups and interpretation of processes affecting water compositions. Groups 1 and 2 discharge from perched-water bodies, and mostly correspond to Na–HCO3 and Na–HCO3–Cl type waters. These groups comprise of cold, thermal (27 °C–75 °C) and boiling waters (92.2 °C–93.2 °C), with a wide TDS range (77.3–27, 145.7 mg/L). Group 3 is made of samples of dominated Na–SO4 from very acid boiling pools (pH range of 2.02–2.27) which are fed by steam-heated perched-water bodies. Group 4 is representative of springs from the basal aquifer system and corresponds to Na–Cl type fluids, with compositions dominated by seawater.Results are used to further develop a conceptual model characterizing the geochemical evolution of the studied waters. Mineral and thermal waters discharging from perched-water bodies are of meteoric origin and chemically evolve by absorption of magmatic volatiles (CO2) and by a limited degree of rock leaching. Existing data also suggest mixture between cold waters and thermal water. Water chemistry from springs that discharge from the basal aquifer system evolves by mixing with seawater; although, processes such as absorption of magmatic volatiles (CO2), rock leaching and mixture with hydrothermal waters are not excluded by the data because the actual composition of these waters deviates from that expected considering only conservative mixing between fresh and seawater.  相似文献   

9.
Abstract

The chemistry of streamwater, bulk precipitation, throughfall and soil waters has been studied for three years in two plantation forest and two moorland catchments in mid-Wales. Na and CI are the major ions in streamwater reflecting the maritime influence on atmospheric inputs. In all streams, baseflow is characterised by high pH waters enriched in Ca, Mg, Si and HCO3. Differences in baseflow chemistry between streams reflect the varying extent of calcite and base metal sulphide mineralization within the catchments. Except for K, mean stream solute concentrations are higher in the unmineralized and mineralized forest catchments compared with their respective grassland counterparts. In the forest streams, storm flow concentrations of H+ are approximately 1.5 times and Al four times higher than in the moorland streams. Annual catchment losses of Na, Cl, SO4, NO3, Al and Si are greatest in the forest streams. In both grassland and forest systems, variations in stream chemistry be explained by mixing waters from different parts of the catchment, although NO3 concentrations may additionally be controlled by N transformations occurring between soils and streams. Differences in stream chemistry and solute budgets between forest and moorland catchments are related to greater atmospheric scavenging by the trees and changes in catchment hydrology consequent on afforestation. Mineral veins within the catchment bedrock can significantly modify the stream chemical response to afforestation.  相似文献   

10.
Water quality analyses for the Niger River for the 1980/81 hydrological year are presented. The samples were collected from the main river at Lokoja, and from two main tributaries, the Kaduna and the Benue Rivers. Different water types were distinguished by the concentrations of major ions. The type Ca > Na > Mg > K - HCO3 > SO4 > Cl was represented at all stations during at least part of the year. Chloride was found to dominate the sulphate ion in the Kaduna and Niger, while the Benue maintained a higher concentration of sulphate relative to chloride all year round. Distinct patterns of seasonal variation in the ion concentrations were observed, particularly for the samples collected at Lokoja. Low ion concentrations were prominent during periods of high discharge, while low flow periods coincided with high dissolved ion concentrations. The contribution of rainwater to the total dissolved solids in the river waters was assessed indirectly using rainwater chemistry data from the Gulf of Guinea. The estimated rainwater contribution to the Lower Niger amounts to 5.15 mg 1?1. Geochemical weathering calculations involving reactions of the four major minerals of granitic rocks - anorthite, biotite, albite, and K-feldspar - with carbon dioxide and water, can account for the average water composition of the Lower Niger. The proportion of the ionic components was also related to the occurrence of the respective element in the minerals.  相似文献   

11.
ABSTRACT

Hydrogeochemical investigations were carried out with an objective to identify the processes affecting the chemistry of groundwater in the Coimbatore district of Tamil Nadu, India. Thirty-three groundwater samples were collected from representative wells for chemical analysis. Groundwater types identified from piper plots were Ca-Mg-Cl and Na-Cl. The dominance of ions was in the order of Na>Ca>Mg>K and Cl>HCO3>SO4>CO3. Spatial variation diagrams of ions were generated using the geostatistical analyst tool ArcGIS 9.3. According to these diagrams, most of the ions were higher in the northeast and southeast regions. This is attributed to the flow direction of the groundwater and high residence times. Gibbs diagrams identified rock–water interaction as an important geochemical process in the district. Evaporation, ion exchange, silicate weathering and dissolution of carbonate minerals were identified as other important hydrogeochemical processes which influence the groundwater chemistry of the study area.
EDITOR D. Koutsoyiannis ASSOCIATE EDITOR M. Besbes  相似文献   

12.
Thermal waters hosted by Menderes metamorphic rocks emerge along fault lineaments in the Simav geothermal area. Thermal springs and drilled wells are located in the Eynal, Çitgöl and Na a locations, which are part of the Simav geothermal field. Studies were carried out to obtain the main chemical and physical characteristics of thermal waters. These waters are used for heating of residences and greenhouses and for balneological purposes. Bottom temperatures of the drilled wells reach 163°C with total dissolved solids around 2225 mg/kg. Surface temperatures of thermal springs vary between 51°C and 90°C. All the thermal waters belong to Na–HCO3–SO4 facies. The cold groundwaters are Ca–Mg–HCO3 type. Dissolution of host rock and ion-exchange reactions in the reservoir of the geothermal system shift the Ca–Mg–HCO3 type cold groundwaters to the Na–HCO3–SO4 type thermal waters. Thermal waters are oversaturated at discharge temperatures for aragonite, calcite, quartz, chalcedony, magnesite and dolomite minerals giving rise to a carbonate-rich scale. Gypsum and anhydrite minerals are undersaturated with all of the thermal waters. Boiling during ascent of the thermal fluids produces steam and liquid waters resulting in an increase of the concentrations of the constituents in discharge waters. Steam fraction, y, of the thermal waters of which temperatures are above 100°C is between 0.075 and 0.119. Reservoir pH is much lower than pH measured in the liquid phase separated at atmospheric conditions, since the latter experienced heavy loss of acid gases, mainly CO2. Assessment of the various empirical chemical geothermometers and geochemical modelling suggest that reservoir temperatures vary between 175°C and 200°C.  相似文献   

13.
The origin and the chemical and isotopic evolution of dissolved inorganic carbon (DIC) in groundwater of the Okavango Delta in semi-arid Botswana were investigated using DIC and major ion concentrations and stable oxygen, hydrogen and carbon isotopes (δD, δ18O and δ13CDIC). The δD and δ18O indicated that groundwater was recharged by evaporated river water and unevaporated rain. The river water and shallow (<10 m) groundwater are Ca–Na–HCO3 type and the deep (≥10 m) groundwater is Na–K–HCO3 to HCO3–Cl–SO4 to Cl–SO4–HCO3. Compared to river water, the mean DIC concentrations were 2 times higher in shallow groundwater, 7 times higher in deep groundwater and 24 times higher in island groundwater. The δ13CDIC indicate that DIC production in groundwater is from organic matter oxidation and in island groundwater from organic matter oxidation and dissolution of sodium carbonate salts. The ionic and isotopic evolution of the groundwater relative to evaporated river water indicates two independent pools of DIC.  相似文献   

14.
A geochemical survey carried out in November 1993 revealed that Lake Quilotoa was composed by a thin (14 m) oxic epilimnion overlying a 200 m-thick anoxic hypolimnion. Dissolved CO2 concentrations reached 1000 mg/kg in the lower stratum. Loss of CO2 from epilimnetic waters, followed by calcite precipitation and a consequent lowering in density, was the apparent cause of the stratification.The Cl, SO4 and HCO3 contents of Lake Quilotoa are intermediate between those of acid–SO4–Cl Crater lakes and those of neutral-HCO3 Crater lakes, indicating that Lake Quilotoa has a ‘memory’ of the inflow and absorption of HC1- and S-bearing volcanic (magmatic) gases. The Mg/Ca ratios of the lake waters are governed by dissolution of local volcanic rocks or magmas, but K/Na ratios were likely modified by precipitation of alunite, a typical mineral in acid–SO4–Cl Crater lakes.The constant concentrations of several conservative chemical species from lake surface to lake bottom suggest that physical, chemical and biological processes did not have enough time, after the last overturn, to cause significant changes in the contents of these chemical species. This lapse of time might be relatively large, but it cannot be established on the basis of available data. Besides, the lake may not be close to steady state. Mixing of Lake Quilotoa waters could presently be triggered by either cooling epilimnetic waters by 4°C or providing heat to hypolimnetic waters or by seismic activity.Although Quilotoa lake contains a huge amount of dissolved CO2 (3×1011 g), at present the risk of a dangerous limnic eruption seems to be nil even though some gas exsolution might occur if deep lake waters were brought to the surface. Carbon dioxide could build up to higher levels in deep waters than at present without any volcanic re-awakening, due to either a large inflow of relatively cool CO2-rich gases, or possibly a long interval between overturns. Periodical geochemical surveys of Lake Quilotoa are, therefore, recommended.  相似文献   

15.
The use of reclaimed water and its impact on groundwater quality in the middle and southern parts of the Jordan Valley are investigated. The chemical analyses indicate that nitrate and bacteriological pollution is widespread, and thus, seriously affects groundwater use. During the study, 365 water samples were collected from wells and springs to determine the water chemistry and the extent of nitrate pollution. Three hydrochemical facies are identifed, i. e., (Ca–(Mg)–Na–HCO3), (Ca–Na–SO4–Cl) and (Ca–Na–Cl). The change of facies is accompanied by a gradual increase in the groundwater total dissolved solids (TDS), which is mainly controlled by evaporates and carbonates dissolution in the aquifer matrix. Water analyses indicate that the shallow aquifer in the study area is affected by non‐point pollution sources, primarily from natural (manure) and chemical nitrogen (N)‐fertilizers and treated wastewater used for agriculture. The concentration of nitrate in the groundwater ranges from 10 to 355 mg/L. Considerable seasonal fluctuations in groundwater quality are observed as a consequence of agricultural practices and other factors such as annual rainfall distribution and the Zarqa River flow. The noticeable levels of total coliform and Escherichia coli in the northern part of the study area may be attributed to contamination from the urban areas, intensive livestock production, and illegal dumping of sewage. Heavy metal concentrations in all samples were found to be significantly lower than the permissible limits for drinking water standards.  相似文献   

16.
Stable isotopic (δDVSMOW and δ18OVSMOW) and geochemical signatures were employed to constrain the geochemical evolution and sources of groundwater recharge in the arid Shule River Basin, Northwestern China, where extensive groundwater extraction occurs for agricultural and domestic supply. Springs in the mountain front of the Qilian Mountains, the Yumen‐Tashi groundwater (YTG), and the Guazhou groundwater (GZG) were Ca‐HCO3, Ca‐Mg‐HCO3‐SO4 and Na‐Mg‐SO4‐Cl type waters, respectively. Total dissolved solids (TDS) and major ion (Mg2+, Na+, Ca2+, K+, SO42?, Cl? and NO3?) concentrations of groundwater gradually increase from the mountain front to the lower reaches of the Guazhou Basin. Geochemical evolution in groundwater was possibly due to a combination of mineral dissolution, mixing processes and evapotranspiration along groundwater flow paths. The isotopic and geochemical variations in melt water, springs, river water, YTG and GZG, together with the end‐member mixing analysis (EMMA) indicate that the springs in the mountain front mainly originate from precipitation, the infiltration of melt water and river in the upper reaches; the lateral groundwater from the mountain front and river water in the middle reaches are probably effective recharge sources for the YTG, while contribution of precipitation to YTG is extremely limited; the GZG is mainly recharged by lateral groundwater flow from the Yumen‐Tashi Basin and irrigation return flow. The general characteristics of groundwater in the Shule River Basin have been initially identified, and the results should facilitate integrated management of groundwater and surface water resources in the study area. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

17.
A comprehensive study of a sandy aquifer of deltaic origin in southern Poland included water chemistry, isotopes, dissolved trace gases and transport modelling. Tritium, sulphur hexafluoride (SF6) and freons (F‐11, F‐12 and F‐113) showed the presence of modern waters in the recharge areas and shallow confined parts of the aquifer. The presence of older Holocene waters farther from the recharge areas was indicated by lack of 3H, SF6 contents ≤0·02 fmol l−1 and relatively low 14C values. The discharge from the system is by upward seepage in the valley of a major river. Pre‐Holocene waters of a cooler climate, identified on the basis of δ18O, δ2H, 14C, Ne and Ar data, were found in some distant wells. Concentrations of N2, Ne and Ar determined by gas chromatography were used for calculating the noble gas temperatures, air excess needed for correction of SF6, and nitrogen content released by denitrification process. The time series of 3H content available for some wells supplied quantitative information on age distributions and the total mean ages of flow through the unsaturated and saturated zones. The derived 3H age distributions turned out to be very wide, with mean values in the range of about 30 to 160 years. For each well with determined 3H age, the SF6 data showed either a lower age range or the possibility of a lower age as expected due to shorter travel times of SF6 through the unsaturated zone, which most probably also resulted in different types of age distributions of these tracers. Freons appeared to be of little use for individual age determinations. A quantitative estimation of two‐component mixing from SF63H relations is not possible unless the travel time of 3H through the unsaturated zone is comparable to that of SF6. The ratio of integrals of the response function over the age range with tracer and the whole response function yields the ratio of water with tracer to total flow of water. That ratio is a tracer‐dependent function of time. Transport modelling of SF6 tracer done with MT3D code yielded initially large discrepancies between calculated and measured tracer concentrations. Some discrepancies remained even after calibration of the transport model with SF6. Simulation of tritium contents with a calibrated transport model yielded reasonable agreement with measured contents in some wells and indicated a need for further investigations, particularly in the eastern part of the aquifer. The existence of distinct hydrochemical zones is consistent with the tracer data; young waters with measurable 3H and SF6 contents are aerobic and of HCO3 Ca or HCO3 SO4 Ca types. Slightly elevated Na and Cl contents, as well as the highest concentrations of SO4 and NO3 within this zone are due to anthropogenic influences. Anaerobic conditions prevail in the far field, under the confining cover, where pre‐bomb era Holocene waters dominate. In that zone, dissolved oxygen, NO3 and U contents are reduced, and Fe, Mn and NH4 contents increase. In the third zone, early Holocene and glacial waters occur. They are of HCO3 Ca Na or HCO3 Na types, with TDS values higher than 1 g l−1 and Na content higher than 200 mg l−1, due to either small admixtures of ascending or diffusing older water or freshening of marine sediments, a process that is probably occurring till the present time. Copyright © 2005 John Wiley & Sons, Ltd.  相似文献   

18.
The analysis of physicochemical variables and selected dissolved elements was performed on the Apure River waters for 15 months. The variables pH, alkalinity, dissolved O2, conductivity and Na, Ca, Mg and Cd concentrations showed maximum values during low water, whereas K, Si, Fe, Al, Mn, Zn, Cu, Cr and dissolved organic carbon (DOC) showed maximum concentrations during rising and high water. Five important factors were found to control the amount and temporal variability of the dissolved elements: lithology, hydrology, vegetation–floodplain processes, redox conditions and organic complexation. Weathering of silicates, carbonates and evaporites in the Andes provides most of the proportion of Na, Ca, Mg and HCO3? to waters. The temporal variability of these ions is controlled by a dilution process. Although Si can be taken up by the biomass, Si and K can be leached from the floodplain by weathering of clays. Microbial decay of the submerged plants in the floodplain during the inundation periods provides DOC and K to river waters and changes the redox conditions in water. The changing redox conditions control the solubility of Mn, Zn and Fe. Dissolved Mn is a function of pH‐dependent redox process, whereas Zn solubility is controlled by scavenging of Zn during the oxidation of Mn2+ to MnO2. Positive relationships between Al, Fe, Cu, Cr and DOC suggest that these elements are complexed by organic colloids generated in the floodplain. Moreover, the binding capacity of Fe with DOC increases under reducing conditions. Although Cd seems to be provided by weathering in the Andes, several processes can affect the mobility of Cd during transport. Copyright © 2010 John Wiley & Sons, Ltd.  相似文献   

19.
Abstract

On the basis of the degree of mineralization, the groundwater of Apan-Tochac sub-basin may be considered as fresh (TDS < 500 ppm). However, chlorination is necessary to make it fit for human consumption. Major ion analyses of over 235 water samples reveal a striking relationship between hydrochemical evolution and the groundwater flow system. A high content of total dissolved solids, and low values of the Ca:Mg ratio are present in wells located on the plain (discharge zone), whereas opposite conditions are associated with wells located in higher regions (recharge zone). Statistical data analysis using the method of principal components allowed to differentiation of two hydrochemical families: (a) low mineralization corresponding to the recharge zone, and (b) high mineralization corresponding to the discharge zone. Waters of the Ca + Mg + HCO3, and Na + Mg + HCO3 hydrochemical fades are present and the former is dominant. The water is slightly alkaline, having slight problems of salinity during the year owing mainly to Ca2+HCO3 ? and Na+Cl? salts. The hydrochemistry of the groundwater reflects the pattern of local groundwater flow for this sub-basin.  相似文献   

20.
Shallow submarine hydrothermal activity has been observed in the Bahía Concepción bay, located at the Gulf coast of the Baja California Peninsula, along faults probably related to the extensional tectonics of the Gulf of California region. Diffuse and focused venting of hydrothermal water and gas occurs in the intertidal and shallow subtidal areas down to 15 m along a NW–SE-trending onshore–offshore fault. Temperatures in the fluid discharge area vary from 50 °C at the sea bottom up to 87 °C at a depth of 10 cm in the sediments.Chemical analyses revealed that thermal water is enriched in Ca, As, Hg, Mn, Ba, HCO3, Li, Sr, B, I, Cs, Fe and Si, and it has lower concentrations of Cl, Na, SO4 and Br than seawater. The chemical characteristics of the water samples indicate the occurrence of mixing between seawater and a thermal end-member. Stable isotopic oxygen and hydrogen composition of thermal samples plot close to the Local Meteoric Water Line on a mixing trend between a thermal end-member and seawater. The composition of the thermal end-member was calculated from the chemistry of the submarine samples data by assuming a negligible amount of Mg for the thermal end-member. The results of the mixing model based on the chemical and isotopic composition indicate a maximum of 40% of the thermal end-member in the submarine vent fluid.Chemical geothermometers (Na/Li, Na–K–Ca and Si) were applied to the thermal end-member concentration and indicate a reservoir temperature of approximately 200 °C. The application of K–Mg and Na/Li geothermometers for vent fluids points to a shallow equilibrium temperature of about 120 °C.Results were integrated in a hydrogeological conceptual model that describes formation of thermal fluids by infiltration and subsequent heating of meteoric water. Vent fluid is generated by further mixing with seawater.  相似文献   

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