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The physicochemical properties and major ion chemistry of the groundwater sources from alluvial aquifers along the stretch (60 km) of Jhelum River in Kashmir Himalaya were determined in order to identify hydro-geochemical processes and their suitability for drinking purposes. The data depicted that calcium and bicarbonates were dominating among the cations and anions. The results indicate the trend of cation dominance as Ca2+ > Na+ > Mg2+ > K+, whereas anion dominance was in the order of HCO3 ? > Cl? > SO4 2?. Ratio of calcium to magnesium indicated the dissolution of Ca2+ from CaCO3, which results in an increased levels of Ca2+ in the groundwater. Interpretation of Piper Trilinear plot understands the various geochemical processes affecting the groundwater quality and shows groundwater was dominated by Ca–HCO3 type. The pH was recorded in the slightly alkalinity range 7.2–7.8 and was showing positive correlation with HCO3 ?. The chloro-alkaline indices revealed 86% of the sources exchange by a type of base-exchange reactions, rest by cation–anion exchange. Gibbs diagram revealed groundwater sources fall in the category of rock dominance. The concentration of the nitrogen compounds was in the progression of NO3–N > NH4–N > NO2–N, and the PO4 ? fluctuated from 0.12 to 0.22 mg/L. Moreover, corrosivity ratio indicated that water from the majority of sources (71%) is safe to supply using pipes without any corrosive effects, while 29% of sources are corrosive in nature and need non-corrosive pipes for transporting and lifting of groundwater. The results revealed, groundwater samples were within permissible limits as prescribed by International and National standards, for drinking purposes. The State government and NGO’s can show their interest in utilizing such water resources to overcome the shortage of drinking water in a sustainable way for the daily consumption of the people living in the vicinity of Jhelum River.  相似文献   

3.
Epidote-bearing porphyritic dikes (whole rock analysis: SiO2?=?55–65 wt. %, MgO <2.1 wt. %, K2O <2.5 wt. %, Al2O3 >17 wt. %, Na2O + K2O?=?5.7–9.4 wt. %) situated in the continental margin zone, the Middle Urals, Russian Federation have been dated using SHRIMP U-Pb zircon techniques and give a Middle Devonian age of 388?±?2 Ma and 389?±?6 Ma. The porphyries contain phenocrysts of magmatic epidote (Ps?=?17–25 %), Ca- and Mn-rich (CaO >9 wt. %; MnO >6 wt. %) almandine garnet, Al-rich (Al2O3?=?12–16 wt. %) amphibole, titanite, plagioclase, biotite, muscovite, apatite, and quartz. 60 to 70 % groundmass of the porphyritic dikes consists of fine-grained albite, quartz, and K-feldspar. A variety of thermobarometric estimations, plus comparison with published experimental data indicate that the phenocryst assemblage was stable between 5 and 11 kbar and 690 to 800 °C. Oxygen fugacity was close to or greater than logfo2 = Ni-NiO + 1. Later stage formation of the quartz-feldspar groundmass took place at hypabyssal conditions, corresponding to 1 to 2 kbar and 660 to 690 °C. The porphyritic dikes are metaluminous to slightly peraluminous (ACNK?=?0.7–1.17). They are enriched in REE and depleted Nb and Ti. They show features typical of subduction-related magmas. Chemical composition and isotopic ratios of 86Sr/87Sri?=?0.709–0.720 suggest that both mantle- and deep crustal-derived materials were involved in their petrogenesis.  相似文献   

4.
The Imphal valley is an intramontane basin confined within an anticlinorium of several anticlines and synclines in the Disang Group of rocks of Tertiary age. This valley of more than 2 million people is occupied by fluvio-lacustrine deposits of Quaternary age and is located in the central part of the Indo-Myanmar range of Northeast India. The hydrogeochemical parameters of temperature, pH, ORP, TDS, Na, Cl, Br, Ba, B, Sr, Li, δ18O, HCO3, K, Mg, Ca, NO3, PO4, SO4 in 173 samples using ion-chromatograph, ICP (AES), ICP (OES), ICP (MS) and 37 dugwells were studied to understand the occurrence and origin of salinization process for the first time. The order of abundance of ions is identified as HCO3 > Na > Cl > Ca > Mg > K > NO3 > PO4 > Sr > Br > B>Ba > Li > SO4. Five hydrochemical facies (Na–Cl, Ca–Mg–HCO3, Na–HCO3, Ca–Mg–HCO3–Cl and Ca–Mg–Cl) represent the types of waters. The saline-dominated water types (Na–Cl and Na–HCO3) represent piedmont and the rest of the facies represent alluvial plain and flood plain groundwaters. Durov’s diagram reveales initial and intermediate stages of groundwater evolution. Isotope δ18O, Gibbs diagram and ions scatter plots suggest evaporation and crystallization processes leading to halite encrustation in the Disang shales. Negative Eh, low NO3 and the absence of SO4 indicates reduced condition coupled with rich dissolve organic matters leading to elevation of salts in soils around piedmont where the rock type is exclusively of the Disang shales. Trilinear plot, correlation matrix and water table flow analysis suggest salinization of groundwater originates in piedmont groundwater and disseminates towards alluvial plain and flood plain along the flow path.  相似文献   

5.
The present work is an effort to develop an appraisal of the hydrogeochemical regime for the aquifers of Dhekiajuli, Sonitpur district, Assam, which is imperative considering: (i) excessive use of groundwater for irrigation; (ii) reported high arsenic (As) contamination; (iii) application of fertilizer is an inevitable process undergoing in this region to achieve higher yield owing to deteriorating water quality; and (iv) study area being the location of many tea estates of Assam, that export tea in many foreign countries. The highest As concentration of 44.39 µg/L was detected in this study (Bachasimalu and Sitalmari region), implying high As-contaminated aquifers being used for drinking and irrigation purposes in the area. The relative abundance pattern of major cations and anions was in the order of Na+ > Mg2+ > Ca2+ > K+ and HCO3 ? > Cl? > SO4 2?, respectively. Majority of the samples belong to Na+–K+–Cl?–HCO3 ? and mixed water type. Closer inspection of Piper plot reveals that a higher As value (>40 µg/L) was prevalent in HCO3 ? water type. Results of hydrogeochemical plots suggest silicate and carbonate weathering, ion exchange and anthropogenic activities to be the dominant processes governing groundwater contamination, including As which is further supported from PCA loadings. The Singri area to the east of the affected areas and adjacent to the Brahmaputra River has oxic aquifers owing to the absence of mass deposition of younger sediments, while reducing conditions prevails in the Bachasimalu and Sitalmari region. High positive correlation between As and Fe (r = 0.83**) and a negative correlation between ORP and Fe (r = ?0.68**) further add that Fe (hydr)oxides are the direct source of As release in the affected region, the mechanism being reductive hydrolysis of such (hydr)oxides. The study implies that although groundwater is suitable for irrigation use, there is a high probability of As getting into the food chain through tea and other edible plants irrigated with As-contaminated water; thus, the area has a maximum probability of facing health hazards caused by As-contaminated groundwater.  相似文献   

6.
The loess–paleosol deposit in Central Asia is a sensitive indicator of the evolution of the quaternary paleoclimate in the Westerlies, providing insight into the quaternary climate history and its relationship with global climatic changes. Based on the geochemical analysis of elemental composition of densely sampled strata from Talede loess–paleosol sequence in the Ili Basin, the results showed that SiO2 had the highest major elements content, followed by Al2O3. The order of compositional abundance of major elements was generally as follows: SiO2 > Al2O3 > CaO > Fe2O3 > MgO > Na2O > K2O. Trace elements (i.e. Rb, Sr, Sc, Ni, Cu, Ga, Mo, Y, Pb, Th) in the paleosol layers (i.e. S 0, S m, S 1) and the loess layer of L 1 were enriched relative to underlain loess (L 2) horizons, except for the contents of Zr, Cs, Nd, and La in paleosol layers. All of geochemical proxies, such as enrichment factor, Rb/Sr ratio, eluvial coefficient (K i ) and chemical weathering index, display no obvious differentiation in the Talede loess–paleosol deposit. The results indicate that the weak chemical weathering, greater evaporation and low effective moisture in Ili Basin, are to a degree weaker than those in the China Loess Plateau and the climate was warm–dry during the interglacial period. In addition, the loess of Ili area is rich in schistose minerals and implies that the loess may come from the deserts of Central Asia and it may be closely related to the widespread aridification of Central Asia.  相似文献   

7.
Prediction of hollows in abandoned underground workings at shallow depth   总被引:1,自引:1,他引:0  
Composite statistical analysis of the lithological composition of the rock mass above underground workings in coal seams and experimental work (laboratory mechanical tests and boring for the determination of hollows) in Donetsk city (Ukraine) have been used to develop a method for predicting the presence of hollows. The empirical criteria K1–K2>0 and K32.5 which relate to the physical characteristics of the overlying strata were found to predict the existence of such hollows in abandoned underground workings at shallow depth. The values of K1–K2 and K3 depend on the thicknesses of the different rock layers and the uniaxial compressive strength of the immediate roof over underground openings. The different layers e.g. sandstones, argillites, aleurolites and alluvium in the rock mass are shown to influence the existence of hollows in abandoned workings. Large thicknesses of sandstones in the rock mass or relatively high uniaxial compressive strength rock in the immediate roof contribute to the existence of hollows in abandoned workings. On the other hand, sandstones of small thickness, weak alluvium, argillites and aleurolites only give additional weight on immediate roof of the opening and allow collapse of the rock mass. The method of prediction for hollows was developed from the back-analysis of data from 41 boreholes which were drilled from the ground surface above underground openings.  相似文献   

8.
The chemical analysis of 19 water wells in Ferdows area, Northeastern Iran, has been evaluated to determine the hydrogeochemical processes and ion concentration background in the region. In the study area, the order of cation and anion abundance is Na+ > Ca2+ > Mg2+ > K+ and Cl? > SO 4 ?2  > HCO3 ? > NO3 ?, respectively, and the dominating hydrochemical types are Na–Cl. Most metal concentrations in water depend on the mineral solubility, and pH, Eh, and salinity of the solution. Their ΣREE concentrations showed excellent correlations with parameters such as TDS and pH. North American Shale Composite (NASC)-normalized REE patterns are enriched in the HREEs relative to the LREEs for all groundwaters. They all have positive Eu anomalies (Eu/Eu* = 0.752–3.934) and slightly negative Ce anomalies (Ce/Ce* = 0.019–1.057). Reduction–oxidation, complexation, desorption, and re-adsorption alter groundwater REE concentrations and fractionation patterns. The positive Eu anomalies in groundwaters are probably due to preferential mobilization of Eu2+ relative to the trivalent REEs in the reducing condition.  相似文献   

9.
Twenty groundwater samples were collected from Enugu metropolis over two seasonal periods in order to characterize the groundwater and to determine its quality for domestic and irrigation purposes. The results show that groundwater of the area is strongly acidic to slightly alkaline in nature and varied from “soft water” to “moderately hard” water type. The major ionic trend is in the order Cl> Na> HCO3 ? > K> Mg2+ > Ca2+ > SO4 2?and Mg2+ > Cl> Na> K> Ca2+ > HCO 3 > SO4 2? in abundance for dry and rainy seasons, respectively. The results also reveal that there is an increase in trend of the ionic concentrations during the dry season, which arises from weathering of the host rocks and anthropogenic activities. Two hydrochemical facies were identified, namely, Na+ –K+ –Cl? –SO4 2?and Ca2+ –Mg2+ –Cl? –SO4 2? , with Na+ –K+ –Cl? –SO4 2? as the dominant facies for the two seasons. Groundwater quality ranges from “very poor water” to “good water” and “water unsuitable for drinking purposes” to “good water” for the dry season and rainy season investigations, respectively. The groundwater is suitable for irrigation purposes for the two seasons.  相似文献   

10.
Hydrogeochemical investigation of groundwater has been carried out in the coastal aquifers of southern Tamil Nadu, India. Seventy-nine dug well samples were collected and analyzed for various physicochemical parameters. The result of the geochemical analysis indicates the groundwater in the study area is slightly alkaline with moderate saline water. The cation and anion concentrations confirm most of the groundwater samples belong to the order of Na+ > Mg2+ > Ca2+ > K+ and Cl? > SO4 2? > HCO3 ?. Thereby three major hydrochemical facies (Ca–Cl, mixed Ca–Mg–Cl and Na–Cl) were identified. Based on the US Salinity diagram, majority of the samples fall under medium to very high salinity with low to high sodium hazard. The cross plot of Ca2+ + Mg2+ versus chloride shows 61 % of the samples fall under saline water category. Higher EC, TDS and Cl concentrations were observed from Tiruchendur to Koodankulam coastal zone. It indicates that these regions are significantly affected by saltwater contamination due to seawater intrusion, saltpan deposits, and beach placer mining activities.  相似文献   

11.
A study was conducted by collecting eight seepage water samples that drain through the sedimentary rocks, mainly sandstone and shale, to evaluate the hydrogeochemical characteristics. The collected samples were analyzed for physico-chemical parameters using standard procedures. Three water types were identified in the Piper plot and the hydrogeochemical evolution starts from a Ca–Cl facies (type 1) via mixed Ca–Mg–Cl and Ca–Na–HCO3 facies (type 2) to Na–Cl facies (type 3). Increasing trend of electrical conductivity (EC) values were observed from type 1 water to type 3 water. Lower ionic concentrations with an average EC value of 35.7 µs/cm in Ca–Cl facies indicate the recharge water by monsoonal rainfall, and ion exchange/weathering process is reflected in the mixing zone. Higher ionic concentration with an average EC value of 399 µs/cm is noted in Na–Cl facies, which indicates the ion exchange during water–rock interaction. Higher log pCO2 values are also found in this facies, revealing the longer residence time of seepage water in the rock matrix, which release more ions into the water. The relative mobility of elements during weathering suggest that the order of mobility in both sandstone and shale is Na > Ca > Mg > K. It was observed that the hydrogeochemistry of seepage water is mainly controlled by the bedrock geology.  相似文献   

12.
13.
Information on the chemical composition of phosphorus (P) fractions in sediments is fundamental to understanding P bioavailability and eutrophication in lake ecosystems. Phosphorus fractions and its bioavailability in sediments cores of Lake Hongfeng, southwest China, were investigated using a chemical sequential extraction scheme. Relationships between P fractions, P bioavailability and particle sizes were discussed. P fractions concentrations were ranked in the order: Residual-P > NaOH–rP > NaOH–NRP > HCl–P > BD–P > NH4Cl–P, and all of them decreased with increasing sediment depth. Statistical analysis showed that concentrations of bioavailable P (BAP) which includes the NH4Cl–P, BD–P, NaOH–rP and NaOH–NRP fractions ranged from 404.68 to 1,591.99 mg/kg and accounted for 26.8–71.8 % of the concentrations of total phosphorus (TP) in the top 5 cm sediments, whereas in the whole sediment cores, their concentrations ranged from 239.70 to 1,591.99 mg/kg and accounted for 26.8–76.0 % of TP. The results suggested that the sediments were a large potential source of P for algae blooms in Lake Hongfeng. Phosphorus fractions and their potential bioavailability were influenced by the sediment particle sizes, especially the bioavailability of the NH4Cl–P fraction, which was strongly affected by the presence of fine particle sizes in the sediments.  相似文献   

14.
With few available soil organic carbon (SOC) profiles and the heterogeneity of those that do exist, the estimation of SOC pools in karst areas is highly uncertain. Based on the spatial heterogeneity of SOC content of 23,536 samples in a karst watershed, a modified estimation method was determined for SOC storage that exclusively applies to karst areas. The method is a “soil-type method” based on revised calculation indexes for SOC storage. In the present study, the organic carbon contents of different soil types varied greatly, but generally decreased with increasing soil depth. The organic carbon content decreased nearly linearly to a depth of 0–50 cm and then varied at depths of 50–100 cm. Because of the large spatial variability in the karst area, we were able to determine that influences of the different indexes on the estimation of SOC storage decreased as follows: soil thickness > boulder content > rock fragment content > SOC content > bulk density. Using the modified formula, the SOC content in the Houzhai watershed in Puding was estimated to range from 3.53 to 5.44 kg m?2, with an average value of 1.24 kg m?2 to a depth of 20 cm, and from 4.44 to 14.50 kg m?2, with an average value of 12.12 kg m?2 to a depth of 100 cm. The total SOC content was estimated at 5.39 × 105 t.  相似文献   

15.
A total of 194 groundwater samples were collected from wells in hard rock aquifers of the Medak district, South India, to assess the distribution of fluoride in groundwater and to determine whether this chemical constituent was likely to be causing adverse health effects on groundwater user in the region. The study revealed that the fluoride concentration in groundwater ranged between 0.2 and 7.4 mg/L with an average concentration of 2.7 mg/L. About 57% of groundwater tested has fluoride concentrations more than the maximum permissible limit of 1.5 mg/L. The highest concentrations of fluoride were measured in groundwater in the north-eastern part of the Medak region especially in the Siddipeta, Chinnakodur, Nanganoor and Dubhaka regions. The areas are underlain by granites which contain fluoride-bearing minerals like apatite and biotite. Due to water–rock interactions, the fluoride has become enriched in groundwater due to the weathering and leaching of fluoride-bearing minerals. The pH and bicarbonate concentrations of the groundwater are varied from 6.6 to 8.8 and 18 to 527 mg/L, respectively. High fluoride concentration in the groundwater of the study area is observed when pH and the bicarbonate concentration are high. Data plotted in Gibbs diagram show that all groundwater samples fall under rock weathering dominance group with a trend towards the evaporation dominance category. An assessment of the chemical composition of groundwater reveals that most of the groundwater samples have compositions of Ca2+–Mg2+–Cl? > Ca2+–Na+–HCO3 ? > Ca2+–HCO3 ? > Na+–HCO3 ?. This suggests that the characteristics of the groundwater flow regime, long residence time and the extent of groundwater interaction with rocks are the major factors that influence the concentration of fluoride. It is advised not to utilize the groundwater for drinking purpose in the areas delineated, and they should depend on alternate safe source.  相似文献   

16.
Groundwater survey has been carried out in the area of Gummanampadu sub-basin located in Guntur District, Andhra Pradesh, India for assessing the factors that are responsible for changing of groundwater chemistry and consequent deterioration of groundwater quality, where the groundwater is a prime source for drinking and irrigation due to non-availability of surface water in time. The area is underlain by the Archaean Gneissic Complex, over which the Proterozoic Cumbhum rocks occur. The results of the plotting of Ca2+ + Mg2+ versus HCO3 ? + CO3 2?, Ca2+ + Mg2+ versus total cations, Na+ + K+ versus total cations, Cl? + SO4 2? versus Na+ + K+, Na+ versus Cl?, Na+ versus HCO3 ? + CO3 2?, Na+ versus Ca2+ and Na+: Cl? versus EC indicate that the rock–water interaction under alkaline condition is the main mechanism in activating mineral dissociation and dissolution, causing the release of Ca2+, Mg2+, Na+, K+, HCO3 ?, CO3 2?, SO4 2? and F? ions into the groundwater. The ionic relations also suggest that the higher concentrations of Na+ and Cl? ions are the results of ion exchange and evaporation. The influences of anthropogenic sources are the other cause for increasing of Mg2+, Na+, Cl?, SO4 2? and NO3 ? ions. Further, the excess alkaline condition in water accelerates more effective dissolution of F?-bearing minerals. Moreover, the chemical data plotted in the Piper’s, Gibbs’s and Langelier–Ludwig’s diagrams, computed for the chloro-alkaline and saturation indices, and analyzed in the principal component analysis, support the above hypothesis. The groundwater quality is, thus, characterized by Na+ > Ca2+ > Mg2+ > K+: HCO3 ? + CO3 2? > Cl? > SO4 2? > NO3 ? > F? facies. On the other hand, majority of groundwater samples are not suitable for drinking with reference to the concentrations of TDS, TH, Mg2+ and F?, while those are not good for irrigation with respect to USSL’s and Wilcox’s diagrams, residual sodium carbonate, and magnesium hazard, but they are safe for irrigation with respect to permeability index. Thus, the study recommends suitable management measures to improve health conditions as well as to increase agricultural output.  相似文献   

17.
To assess the competitive sorption and desorption of cadmium (Cd) and lead (Pb), batch equilibrium experiments were performed using single- and binary-metal solutions in surface samples of three paddy soils from eastern China. Sorption isotherms were well fitted with one-metal and competitive Langmuir equation for single- and binary-metal system, respectively. The distribution coefficient (K d) values were K d single (Pb) > K d binary (Pb) > K d single (Cd) > K d binary (Cd), indicating that Pb was stronger sorbed by these soils than Cd in binary metal system. Soils with high pH and clay content had the greatest sorption capacity as estimated by the maximum sorption parameter (Q). The co-existence of both metals reduces their tendency of sorption, whereas Cd sorption was affected to a greater extent than that of Pb. The Langmuir binding strength parameter (b) in binary sorption system was greater than that in single sorption system for all soils (b < b 1), indicating that competition for sorption sites promote the retention of both metals into more specific sorption sites. Sorption of Cd and Pb decreased soil pH by 1.61 U for YRS, 1.39 U for PCS, and 0.91 U for SLS. The decreases of pH in binary metal system were greater than in single-metal system for three soils. Cadmium and Pb desorption increased with increasing Cd and Pb sorption saturation for all soils; however, Cd desorption ratio in binary metal system (d Cd*) was much greater than Pb (d Pb*), indicating that under the competitive sorption conditions, the sorbed Cd was more readily desorbed from the soils than the sorbed Pb.  相似文献   

18.
Voluminous Neoproterozoic granitoid sheets of the Imorona–Itsindro Suite are important components of exposed basement in west-central Madagascar. Here, we report precise new zircon U–Pb ages and whole-rock geochemistry for granitoids within the Maevatanana area of Madagascar. The new laser ablation inductively coupled plasma mass spectrometry zircon U–Pb dating undertaken during this study indicates that Antanimbary granitoid and Antasakoamamy granitoid were emplaced at 747 ± 9 Ma and 729 ± 9–727 ± 8 Ma, respectively. Geochemically, the Antanimbary granitoids show poor Nb, Ta anomalies, pronounced positive Zr anomalies, and are K-rich (K2O/Na2O > 1), but the Antasakoamamy granitoids are relatively depleted in Nb, Ta, show slightly negative Zr anomalies, and are Na-rich (Na2O/K2O > 1). Both suites contain zircons with strongly negative εHf(t), indicating participation of much older (Palaeoproterozoic and Archaean) crust. Their geochemical characteristics, along with the use of various discrimination diagrams, reveals that crustal delamination and asthenospheric upwelling resulted in crustal extension of the region before ~747 Ma, with subsequent lithospheric subduction and arc magmatism after 729–727 Ma.  相似文献   

19.
Groundwater of an aquifer located in the vicinity of a large coal washery near Zarand City, Iran consists of two hydrochemically differing facies, which have been informally designated as groundwater (A) and groundwater (B). Groundwater (A) is native, brackish in composition and is characterized by Na+ > Mg2+ > Ca2+ > K+ and SO4 2? > HCO3 ? > Cl? > NO3 ?. Spearman’s rank correlation coefficient matrices, factor analysis data, and values of chloro-alkaline indices, C ratio and Na+/Cl? molar ratio indicate that in the groundwater (A), the ionic load of Ca2+, Mg2+, Na+, K+, SO4 2? and HCO3 ? is derived essentially from weathering of both carbonates and aluminosilicates and direct cation and reverse cation–anion exchange reactions. Groundwater (B) is the polluted variant of the groundwater (A), brackish to saline in composition, and unlike the groundwater (A), consists of HCO3 ? as the dominant anion. In comparison with the groundwater (A), the groundwater (B) contains higher concentrations of all ions, and its average ionic load (av. = 59.74 me/L) is 1.43 times higher than that of the groundwater (A) (av. = 41.54 me/L). Additional concentrations of Ca2+, Mg2+, K+, SO4 2?, Cl? and HCO3 ? in the groundwater (B) are provided mainly by downward infiltrating water from the coal washery tailings pond and reverse cation–anion exchange reaction between tailings pond water and exchanger of the aquifer matrix during non-conservative mixing process of groundwater (A) and tailings pond water. Certain additional concentrations of Na+, K+ and NO3 ? in the groundwater (B) are provided by other anthropogenic sources. Quality wise, both groundwaters are marginally suitable for cultivation of salt-tolerant crops only.  相似文献   

20.
Deepawali is one of the main festivals for Hindu religion which falls in the period October–November every year with great fireworks display. In this study, we investigated the levels of water soluble ions and heavy metals—during the fireworks festival in Rajnandgaon, Central India. The chemical compositions and noise level distributions are reported from the sampling site. First time during Deepawali, air quality was studied in this area, The Aerosol samples of PM10 (particle aerodynamic diameter <10 μm) are collected in October 24–28, 2011. Aims of the present studies are (1) To describe the particulate concentrations and associated chemical species during Deepawali festival, (2) To recognize the noise level in Deepawali festival. For study, the samples were collected in glass fiber filter paper and analyzed for the major water soluble ions F?, Cl?, NO3 ?, SO4 2?, Na2+, NH4 +, K+, Ca2+, and Mg2+ employing ion chromatograph. Concentration of heavy metals was analyzed by ICP-MS and was observed to occur in order Fe > Zn > Pb > Ni > Cr > Cd. The result revels that all concentration are above the permissible limit fixed by CPCB, USPEA, and WHO standard. It is concluded that the burning of fireworks during Deepawali festival was the main source of heavy metals and ion.  相似文献   

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