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1.
This study investigated the effect of a pine/oak forest canopy on rainfall chemistry in the Qinling Mountains. The area is an important water source for China’s North-to-South Water Transfer Project. Rainfall and throughfall samples were collected at the Huoditang Natural Forest in 1999, 2004, and 2009. Analyses of the samples indicated that the forest canopy had several important effects on rainfall chemistry. Rainfall pH generally increased as water passed through the canopy. On average, the rainfall pH increased by 0.54 pH units. The canopy’s effect declined after deciduous trees lost their leaves late in the sampling season. Rainfall NO3 ? concentrations generally declined as water passed through the forest canopy, but PO4 3? concentrations generally increased. On average, rainfall NO3 ? concentration declined by 0.135 mg/L as it passed though the forest canopy and PO4 3? increased by 0.85 mg/L. The forest canopy had a mitigating effect on the base cation content of throughfall. Specifically, K+, Na+, Ca2+ and Mg2+ were leached from the canopy when the concentration of these cations in rainfall was low. In contrast, K+, Na+, Ca2+ and Mg2+ were absorbed by the canopy when the concentration of these cations in rainfall was high. The pH of rainfall, as well as its K+, Ca2+ and Mg+ concentration, influenced the effect of the forest canopy on the base cation content of throughfall. The concentration of Cd, Pb, and Zn in rainfall generally decreased as water passed through the forest canopy, but the concentration of Fe in rainfall generally increased. The Cd concentration decreased by an average of 3.938 μg/L, the Pb concentration decreased by an average of 8.457 μg/L, and the Zn concentration decreased by an average of 0.986 mg/L. The Fe concentration increased by an average of 0.009 mg/L. The canopy’s ability to absorb Cd declined after several rainfall events in which rainfall Cd concentrations were relatively high.  相似文献   

2.
Hydrochemical investigations were carried out in Damagh area, Hamadan, western Iran, to assess chemical composition of groundwater. Forty representative groundwater samples were collected from different wells to monitor the water chemistry of various ions. Chemical analysis of the groundwater showed that the mean concentration of the cations is in the order Na+ > Ca2+ > Mg2+ > K+, while that for anions was HCO3− > Cl− > SO42 − > NO3−. All of the investigated groundwaters present two different chemical facies (Ca–HCO3 and Na–HCO3) which is in relation with their interaction with the geological formations of the basin, cation exchange between groundwater and clay minerals and anthropogenic activities. The principal component analysis (PCA) performed on groundwater identified three principal components controlling their variability in groundwater. Electrical conductivity, Mg2+, Na+, SO42−, and Cl− content were associated in the same component (PC1) (salinity), determined principally by anthropogenic activities. The pH, CO32 −, HCO3−, and Ca2+ (PC2) content were related to the geogenic factor. Finally, the NO3−, Cl− and K+ (PC3) were controlled by anthropogenic activity as a consequence of inorganic fertilizers.  相似文献   

3.
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   

4.
The present study highlights the hydrogeological and hydrogeochemical characteristics of the CO2-rich thermal–mineral waters in Kayseri, Turkey. These waters of Dokuzpınar cold spring (DPS) (12–13°C), Yeşilhisar mineral spring (YMS) (13–16°C), Acısu mineral spring (ACMS) (20–22.5°C), Tekgöz thermal spring (TGS) (40–41°C), and Bayramhacı thermal-mineral spring (BTMS) (45–46.5°C) have different physical and chemical compositions. The waters are located within the Erciyes basin in the Central Anatolian Crystalline complex consisting of three main rock units. Metamorphic/crystalline rocks occur as the basement, sedimentary rocks of Upper Cretaceous-Quaternary age form the cover, and volcanosedimentary rocks Miocene-Quaternary in age represent the extrusive products of magmatism acting in that period. All these units are covered unconformably by terrace and alluvial deposits, and travertine occurrences have variable permeability. Dokuzpinar cold spring, YMS and ACMS localized mainly along the faults within the region have higher Na+ and Cl− contents whereas TGS and BTMS have higher amounts of Ca2+ and HCO 3 − . The high concentrations of Ca2+ and HCO 3 − are mainly related to the high CO2 contents resulting from interactions with carbonate rocks. Whereas the high Na+ content is derived from the alkaline rocks, such as syenite, tuff and basalts, the Cl− is generally connected to the dissolution of the evaporitic sequences. These waters are of meteoric-type. BTMS deviates from meteoric water line. The content is related to the increases in the δ18O compositions due to mineral–water interaction (re-equilibrium) process. CO2-dominated YMS and ACMS with low temperatures have higher mineralizations. Yeşilhisar mineral spring, ACMS, TGS and BTMS are oversaturated in terms of calcite, aragonite, dolomite, goethite and hematite, and undersaturated with respect to gypsum, halite and anhydrite. Yeşilhisar mineral spring, ACMS and BTMS are also characterized by recent travertine precipitation. Dokuzpınar cold spring is undersaturated in terms of the above minerals. The higher ratios of Ca/Mg and Cl/HCO3, and lower ratios of SO4/Cl in BTMS than TGS suggest that TGS has shallow circulation compared to BTMS, and/or has much more heat-loss enroute the surface. The sequence of hydrogeochemical and isotopic compositions of the waters is in an order of DPS>YMS>ACMS>TGS>BTMS and this suggests a transition period from a shallow circulation to a deep circulation path.  相似文献   

5.
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   

6.
Geochemical processes that take place in the aquifer have played a major role in spatial and temporal variations of groundwater quality. This study was carried out with an objective of identifying the hydrogeochemical processes that controls the groundwater quality in a weathered hard rock aquifer in a part of Nalgonda district, Andhra Pradesh, India. Groundwater samples were collected from 45 wells once every 2 months from March 2008 to September 2009. Chemical parameters of groundwater such as groundwater level, EC and pH were measured insitu. The major ion concentrations such as Ca2+, Mg2+, Na+, K+, Cl−, and SO4 2− were analyzed using ion chromatograph. CO3 − and HCO3 − concentration was determined by acid–base titration. The abundance of major cation concentration in groundwater is as Na+ > Ca2+ > Mg2+ > K+ while that of anions is HCO3 − > SO4 2− > Cl− > CO3 −. Ca–HCO3, Na–Cl, Ca–Na–HCO3 and Ca–Mg–Cl are the dominant groundwater types in this area. Relation between temporal variation in groundwater level and saturation index of minerals reveals the evaporation process. The ion-exchange process controls the concentration of ions such as calcium, magnesium and sodium. The ionic ratio of Ca/Mg explains the contribution of calcite and dolomite to groundwater. In general, the geochemical processes and temporal variation of groundwater in this area are influenced by evaporation processes, ion exchange and dissolution of minerals.  相似文献   

7.
Two springs (Cuihua Spring, Shuiqiuchi Spring) in Cuihua Mountain of the Qinling Mountains were observed and sampled monthly during 2004 and 2005 to trace their physical properties and chemical compositions with seasons. Although both pH values and cation (Ca2+, Mg2+, K+, and Na+) contents of Cuihua Spring are higher than those of Shuiqiuchi Spring, seasonal variations in both springs are obvious. The pH values of both spring waters are between 5.69 and 6.98, lower than that of rainwater during summer and autumn. From January to November, the pH values of both springs similarly vary from high to low and then to high again. Variations in electric conductivities of two spring waters are contrary, although their electric conductivities are positively correlative with the cation content respectively. This can be attributed to different water sources of the two springs or different acidic rocks they passed. The contents of HCO3 −, Ca2+, Mg2+, K+, and Na+ are low, indicating a low silicate weathering that the strata in this district are mainly composed of granite and schist of quartz and mica. Differing from change in spring water in karst regions of South China where abundant precipitation and dilution of rainwater cause low pH and electric conductivity in summer and autumn, the seasonal variations in the pH values and the electric conductivities of two springs in Qinling Mountains are attributed to seasonal changes in CO2 produced by microorganisms’ activity in soil within respective year, rather than rainfall. The microorganisms’ activity in soil produces more CO2 during summer and autumn. Therefore, the water nature of springs in silicate regions chiefly reflects the seasonal changes of CO2 produced by the microorganisms in soil.  相似文献   

8.
This study was conducted to evaluate factors regulating groundwater quality in an area with agriculture as main use. Thirty groundwater samples have been collected from Razan area (Hamadan, Iran) for hydrochemical investigations to understand the sources of dissolved ions and assess the chemical quality of the groundwater. The chemical compositions of the groundwater are dominated by Na+, Ca2+, HCO3 −, Cl− and SO4 2−, which have been derived largely from natural chemical weathering of carbonate, gypsum and anthropogenic activities of fertilizer’s source. The production of SO4 2− has multiple origins, mainly from dissolution of sulphate minerals, oxidation of sulphide minerals and anthropogenic sources. The major anthropogenic components in the groundwater include Na+, Cl−, SO4 2− and NO3 −, with Cl− and NO3 − being the main contributors to groundwater pollution in Razan area.  相似文献   

9.
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   

10.
Hydrogeochemical investigations are carried out in the different blocks of Burdwan district, West Bengal, India in order to assess its suitability for drinking as well as irrigation water purpose. Altogether 49 representative groundwater samples are collected from bore wells and the water chemistry of various ions viz. Ca2+, Mg2+, Na+, K+, CO32−, HCO3−, Cl−, SO42− and NO3− are carried out. The chemical relationships in Piper and Gibbs diagram suggest that the groundwater mainly belongs to alkali type and Cl− group and are controlled by rock dominance. A comparison of groundwater quality in relation to drinking water quality standards proves that most of the water samples are suitable for drinking water purpose whereas groundwater in some areas of the district has high salinity and high sodium adsorption ratio (SAR), indicating unsuitability for irrigation water and needs adequate drainage.  相似文献   

11.
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   

12.
The formation of the Mufushan granopegmatite was closely related to the Late Yenshanian multiphase and multistage magmatic activities,More than one generation of beryl and aquamarine occur in different types of pegmatite in the granites.The presence of melt and melt-fluid inclusions strongly indicates a melt-solution character of the pegmatitic magma.Forming temperatures of the different generations of beryl in a Na^ -K^ ,Ca^2 -CO3^2--Cl^--SO4^2- solution ranges from 990℃to 200℃.Aquamarine was formed at 720-180℃.The contents of alkali metals(Na^ K^ )in th ore-formming solution of aquamarine are lower than those in the beryl,but the contents of alkali earths(Ca) and salinity are higher,The granite was generated by remelting of the basement formation(meta-sedimentary rocks of the Lengjiaxi Group)which also served as the source of ore-forming material.Beryllium in the pegmatite was transported mainly in the form of Na[Be(CO3)2],with part of it being complexed with Cl^- and SO4^2-.During the generation and evolution of the pegmatite,equilibrium might have been reached in the solid-melt-fluid or solid-fluid system.The intergranular solutions may have reacted with the early crystallized minerals,resulting in potash-feldsparization,albitization and muscovitization during which the ore-forming elements were mobilized and transported in favour of ore deposition.  相似文献   

13.
THEJINLONGSHANGOLDOREBELTINZHEN’ANCOUN TY,SOUTHERNSHAANXIPROVINCE,ISLOCATEDINTHEWEST ERNQINLINGGOLDPROVINCE(NO.16INFIG.1;CHEN YANJINGETAL.,2004).ITWASDISCOVEREDINTHEDEVO NIANSTRATAINTHELATE1980S).ITSGEOLOGICALSETTING ANDMETALLOGENICEVOLUTIONARESIMILARTOT…  相似文献   

14.
Groundwater in Palnad sub-basin is alkaline in nature and Na+-Cl−-HCO3− type around Macherla-Karempudi area in Guntur district, Andhra Pradesh. Total dissolved solids (TDS) show strong positive correlation with Cl−, Na+, Ca2+ and Mg2+, and positive correlation with SO42−, K+ and HCO3−. Calcareous Narji Formation is the dominant aquifer lithology, and water-rock interaction controls the groundwater chemistry of the area. Chloro-alkaline indices (CAI) are positive at Miriyala, Adigopula, Mutukuru, Macherla and Durgi suggesting replacement of Na+ and K+ ions from water by Mg++ and Ca++ ions from country rock through base exchange reactions. Negative CAI values are recorded at Terala, Rayavaram and Nehrunagar, which indicate exchange of Na+ and K+ from the rock as cation-anion exchange reaction (chloro-alkaline disequilibrium). TDS range from 91 to 7100 ppm (Avg. 835 ppm) and exceed the prescribed limit of drinking water around Mutukuru, Durgi, Rayavaram, Khambampadu and Ammanizamalmadaka areas. Scanty rainfall and insufficient groundwater recharge are the prime factors responsible for high salinity in the area. Fluoride content ranges from <1 to 3.8 ppm and contaminated areas were identified around Macherla (1 sq km; 3.8ppm), Mandadi (1 sq km, 2.1ppm) and Adigopula (2 sq km, <1 to 3.7 ppm). The % Na+ content varies from 17 to 85 with the mean value of 57, and eighty (80) samples showed higher %Na+ in comparison to the prescribed limit of 60 for irrigation water. Sodium Adsorption Ratio (SAR) and % Na+ in relation to total salt concentration indicate that groundwater (51%) mostly falls under doubtful to poor quality for irrigation purpose. Groundwater of Adigopula village is fluoride contaminated and remedial measures are suggested to improve the water quality.  相似文献   

15.
The Heihe River Basin is a typical arid inland river basin for examining stress on groundwater resources in northwest China. The basin is composed of large volumes of unconsolidated Quaternary sediments of widely differing grain size, and during the past half century, rapid socio-economic development has created an increased demand for groundwater resources. Understanding the hydrogeochemical processes of groundwater and water quality is important for sustainable development and effective management of groundwater resources in the Heihe River basin. To this end, a total of 30 representative groundwater samples were collected from different wells to monitor the water chemistry of various ions and its quality for irrigation. Chemical analysis shows that water presents a large spatial variability of chemical facies (SO4 2−–HCO3−, SO4 2−–Cl−, and Cl−–SO4 2−) as groundwater flow from recharge area to discharge area. The ionic ratio indicates positive correlation between the flowing pairs of parameters: Cl− and Na+(r = 0.95), SO4 2− and Na+ (r = 0.84), HCO3 − and Mg2+(r = 0.86), and SO4 2− and Ca2+ (r = 0.91). Dissolution of minerals, such as halite, gypsum, dolomite, silicate, and Mirabilite (Na2SO4·10H2O) in the sediments results in the Cl−, SO4 2−, HCO3 −, Na+, Ca2+ and Mg2+ content in the groundwater. Other reactions, such as evaporation, ion exchange, and deposition also influence the water composition. The suitability of the groundwater for irrigation was assessed based on the US Salinity Laboratory salinity classification and the Wilcox diagram. The results show that most of the groundwater samples are suitable for irrigation uses barring a few locations in the dessert region in the northern sub-basin.  相似文献   

16.
In this study, the hydrochemical characteristics of shallow groundwater in a coastal region (Khulna) of southwest Bangladesh have been evaluated based on different indices for drinking and irrigation uses. Water samples were collected from 26 boreholes and analyzed for major cations and anions. Other physico-chemical parameters like pH, electrical conductivity (EC), and total dissolved solids were also measured. Most groundwater is slightly alkaline and largely varies in chemical composition, e.g. EC ranges from 962 to 9,370 μs/cm. The abundance of the major ions is as follows: Na+ > Ca2+ > Mg2+ > K+ = Cl− > HCO3 − > SO4 2− > NO3 −. Interpretation of analytical data shows two major hydrochemical facies (Na+–K+–Cl−–SO4 2− and Na+–K+–HCO3 −) in the study area. Salinity, total hardness, and sodium percentage (Na%) indicate that most of the groundwater samples are not suitable for irrigation as well as for domestic purposes and far from drinking water standard. Results suggest that the brackish nature in most of the groundwaters is due to the seawater influence and hydrogeochemical processes.  相似文献   

17.
Pollution of groundwater by seawater intrusion poses a threat to sustainable agriculture in the coastal areas of Korea. Therefore, seawater intrusion monitoring stations were installed in eastern, western, and southern coastal areas and have been operated since 1998. In this study, groundwater chemistry data obtained from the seawater intrusion monitoring stations during the period from 2007 to 2009 were analyzed and evaluated. Groundwater was classified into fresh (<1,500 μS/cm), brackish (1,500–3,000 μS/cm), and saline (>3,000 μS/cm) according to EC levels. Among groundwater samples (n = 233), 56, 7, and 37% were classified as the fresh, brackish, and saline, respectively. The major dissolved components of the brackish and saline groundwaters were enriched compared with those of the fresh groundwater. The enrichment of Na+ and Cl− was especially noticeable due to seawater intrusion. Thus, the brackish and saline groundwaters were classified as Ca–Cl and Na–Cl types, while the fresh groundwater was classified as Na–HCO3 and Ca–HCO3 types. The groundwater included in the Na–Cl types indicated the effects of seawater mixing. Ca2+, Mg2+, Na+, K+, SO4 2−, and Br− showed good correlations with Cl− of over r = 0.624. Of these components, the strong correlations of Mg2+, SO4 2−, and Br− with Cl− (r ≥ 0.823) indicated a distinct mixing between fresh groundwater and seawater. The Ca/Cl and HCO3/Cl ratios of the groundwaters gradually decreased and approached those of seawater. The Mg/Cl, Na/Cl, K/Cl, SO4/Cl, and Br/Cl ratios of the groundwaters gradually decreased, and were similar to or lower than those of seawater, indicating that Mg2+, Na+, K+, SO4 2−, and Br−, as well as Cl− in the saline groundwater can be enriched by seawater mixing, while Ca2+ and HCO3 − are mainly released by weathering processes. The influence of seawater intrusion was evaluated using threshold values of Cl− and Br−, which were estimated as 80.5 and 0.54 mg/L, respectively. According to these criteria, 41–50% of the groundwaters were affected by seawater mixing.  相似文献   

18.
Fluid chemistry and processes at the Porgera gold deposit, Papua New Guinea   总被引：4，自引：0，他引：4  
The Porgera gold deposit in Papua New Guinea is a world-class example of an alkalic-type epithermal gold system (stage II), which overprints a precursor stage of magmatic-hydrothermal gold mineralization (stage I). Gas and ion chromatographic analyses of fluid inclusions contained in vein minerals from both mineralization stages have been carried out in order to constrain the compositions of the fluids involved in, and the processes attending, ore deposition. These data indicate the presence of three end-member liquids, the most dilute of which was present throughout the mineralization history and is interpreted to represent evolved groundwater of meteoric origin. Its composition is estimated to have been approximately 500 mM Na+, 10 mM K+, 5 mM Li+, 250 mM Cl−, 0.15 mM Br−, and 0.01 mM I−, plus significant concentrations of dissolved gases. More saline liquids were also present during the two main stages of ore formation, and although their compositions differ, both are interpreted to have been derived at least in part from magmatic fluids, and to have been the media by which gold was introduced into the system. Stage I minerals contain fluid inclusions which decrease in salinity towards this dilute end-member composition through the vein paragenesis, reflecting progressive dilution at depth of the magmatic fluid source by groundwaters. Ore deposition is thought to have been caused largely by simple cooling and/or wallrock reactions, although limited in situ fluid mixing may also have occurred. The most saline fluids, present in early quartz and pyrite, contain at least 810 mM Na+, 530 mM Ca2+, 130 mM K+, 12 mM Li+, 87 mM SO4 2−, 960 mM Cl−, 1.1 mM Br−, and 0.05 mM I−, plus significant but variable concentrations of dissolved gases. Fluid inclusions from stage II hydraulic breccia veins reveal the presence of two distinct liquids with contrasting salinities, which were present at different times during vein formation. A higher salinity liquid appears to have predominated during mineralization, whereas lower salinity groundwaters filled the structures during intervening periods. The ore-forming fluid may have been forcibly injected into the veins from depth during fracturing and depressurization events, displacing the resident groundwaters in the process. The original composition of this fluid is estimated to have been at least 1770 mM Na+, 59 mM K+, 180 mM Li+, 210 mM SO4 2−, 680 mM Cl−, 1.4 mM Br−, and 0.09 mM I−, plus 1.5 mol% CO2, 0.19 mol% CH4, and 0.04 mol% N2. Gas chromatographic analyses of fluid inclusions from stage II samples show a decrease in total gas content between early unmineralized veins and post-mineralization vuggy quartz (suitable samples could not be obtained from the ore stage itself). Post-mineralization samples plot along an experimental gas-saturation curve in the CO2-CH4-H2O-NaCl system, obtained at conditions similar to those attending stage II ore deposition at Porgera (200–300 bar, ˜165 °C). These results are interpreted to indicate a period of depressurization-induced phase separation during hydraulic fracturing, which resulted in rich ore deposition. Volatile gases such as CH4 and N2, in addition to CO2 in solution, are shown to have a significant negative effect on total gas solubility. This effect may be of critical importance in lowering the temperature and increasing the depth (pressure) at which phase separation can occur in epithermal systems. Received: 28 November 1995 / Accepted: 17 July 1996  相似文献   

19.
The area in Guntur district, Andhra Pradesh, India, is selected to discuss the impact of seasonal variation of groundwater quality on irrigation and human health, where the agriculture is the main livelihood of rural people and the groundwater is the main source for irrigation and drinking. Granite gneisses associated with schists and charnockites of the Precambrian Eastern Ghats underlie the area. Groundwater samples collected seasonally, pre- and post-monsoons, during three years from forty wells in the area were analyzed for pH, EC, TDS, TA, TH, Ca2+, Mg2+, Na+, K+, CO32−, HCO3−, Cl−, SO42−, NO3−and F−. The chemical relationships in Piper’s diagram, Chebotarev’s genetic classification and Gibbs’s diagram suggest that the groundwaters mainly belong to non-carbonate alkali type and Cl− group, and are controlled by evaporation-dominance, respectively, due to the influence of semi-arid climate, gentle slope, sluggish drainage conditions, greater water–rock interaction, and anthropogenic activities. A comparison of the groundwater quality in relation to drinking water quality standards proves that most of the water samples are not suitable for drinking, especially in post-monsoon period. US Salinity Laboratory’s and Wilcox’s diagrams, and %Na+ used for evaluating the water quality for irrigation suggest that the majority of the groundwater samples are not good for irrigation in post-monsoon compared to that in pre-monsoon. These conditions are caused due to leaching of salts from the overlying materials by infiltrating recharge waters. A management plan is suggested for sustainable development of the area.  相似文献   

20.
Slate quarrying in Mahendragarh district of Haryana state has resulted in changes in soil properties. Most of the mining area is devoid of vegetation. The soil in and around the mining area (0–1 km) is alkaline (pH 11.2–11.7) but non-saline (electrical conductivity < 4). The alkaline nature of the soil was attributed to the high concentrations of hydroxyl (OH−), carbonate (CO32−) and bicarbonate (HCO3 −) present in minerals of mined materials. Biotite, limonite, kaolinite, gibbsite, muscovite, geothite, dolomite and so on were the chief minerals added to soil through mining. The physical properties of soil, i.e. porosity, water-holding capacity (WHC), bulk density and particle density represented poor soil health in mining area (34.4, 29.8%, 1.636, 2.496 g/cc, respectively) and they improved with distance away from it (46.4, 38.3%, 1.070, 2.180 g/cc, respectively, at a distance of 1 km). Porosity and WHC were found to be a function of increased organic matter away from the mining area. CO32−, HCO3−, phosphate (PO43−), lead (Pb) and iron (Fe) were more in mining area and decreased with distance. On the other hand, sodium (Na+), potassium (K+), chloride (Cl−), sulphate (SO42−), organic carbon, total Kjeldahl’s nitrogen, cation exchange capacity, chromium (Cr) and cadmium (Cd) increased with distance from mining area. High concentration of heavy metals in mining area was a cause of concern (0.93 μg/g Cd, 22.35 μg/g Cr, 26.25 μg/g Pb, 1,383.75 μg/g Fe). The change in physico-chemical properties could be because of the addition of chemical constituents that are a part of major minerals present in mined material. The soil away from mining area represented comparatively better properties.  相似文献   

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