Assessment of water quality in the Messolonghi�CEtoliko and Neochorio region (West Greece) using hydrochemical and statistical analysis methods

Assessment of the water quality can enhance understanding of the hydrochemical system and effective management of water resources. To this end, an assessment of water quality was conducted in the Messolonghi-Etoliko and Neochorio region. Surface water and groundwater samples have been collected, treated, and subjected to chemical analysis for the following parameters: Br?, Cl?, F?, NO??, NO??, PO?3?, SO?2?, Li?, Na?, NH??, K?, Mg2?, Ca2?, HCO??, Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb, and Zn. A characterization has been carried out using the Piper trilinear diagram, the United States Salinity Laboratory diagram, and the Wilcox diagram. Assessment of water samples by comparing the recorded values of the water quality parameters with the parametric values established by European Community indicated that the 50% of the surface water samples and 67% of the groundwater samples in the study area are chemically suitable for drinking use. Assessment of water samples from calculation of chemical indexes like sodium adsorption ratio, sodium percentage, residual sodium carbonate, and by comparing the values of the water quality parameters with the water quality limits established by Canadian Council of Minister of the Environment indicated that 75% of the surface water and that all the groundwater samples are chemically suitable for irrigation use.     

Ion chemistry and individual particle analysis of atmospheric aerosols over Mt. Bogda of eastern Tianshan Mountains, Central Asia

Aerosol samples were collected during the scientific expedition to Mt. Bogda in July-August, 2009. The major inorganic ions (Na(?+?), NH??, K(?+?), Mg(2?+?), Ca(2?+?), Cl(?-?), SO2??, and NO??) of the aerosols were determined by ion chromatography. SO2??, NO??, and Ca(2?+?) were the dominate ions, with the mean concentrations of 0.86, 0.56, and 0.28 μg m?3, respectively. These mean ion concentrations were generally comparable with the background conditions in remote site of Xinjiang, while much lower than those in ürümqi. Morphology and elemental compositions of 1,500 particles were determined by field emission scanning electron microscopy equipped with an energy dispersive X-ray spectrometer. Based on the morphology and elemental compositions, particles were classed into four major groups: soot (15.1%), fly ash (4.7%), mineral particles (78.9%), and little other matters (0.8% Fe-rich particles and 0.5% unrecognized particles). Presence of soot and fly ash particles indicated the influence of anthropogenic pollutions, while abundance mineral particles suggested that natural processes were the primary source of aerosols over this region, coinciding with the ionic analysis. Backward air mass trajectory analysis suggested that ürümqi may contribute some anthropogenic pollution to this region, while the arid and semi-arid regions of Central Asia were the primary source.     

Statistical approaches for hydrogeochemical characterization of groundwater in West Delhi, India

Parametric statistical approaches, correlations and multiple linear regressions were used to develop models for the interpretation of hydrogeochemical parameters in the Western part of Delhi state, India. The hydrogeochemical parameters indicated that the groundwater quality is not safe for consumption. The water is moderately saline and the salinity level is increasing over time. There is also the problem of nitrate pollution. The correlation between electrical conductivity (EC) and other water quality parameters except potassium (K(+)), nitrate (NO(3)(-)) and bicarbonate (HCO(3)(-)) is significantly positive and Ca(++)+ Mg(++)/Na(+)+ K(+) is significantly negative. In predicting EC, the multiple R(2) values of 0.996 and 0.985 indicate that 99.6% and 98.5% variability in the observed EC could be ascribed to the combined effect of Na(+), HCO(3)(-), Cl(-), SO(4)(--), NO(3)(-) and Ca(++)+ Mg(++) for the year of 2005 and 2006 respectively. Out of 99.6% of the variability in EC in 2005, 51.2% was due to Cl(-) alone, and 8.5%, 12.5%, 6.1%, 14.7% and 6.7% were due to Na(+), HCO(3)(-), SO(4)(--), NO(3)(-) and Ca(++) + Mg(++). Similarly in 2006, out of 98.5% of the variability in EC, 48.5% was due to Cl(-) alone, and 10.4%, 12.7%, 5.3%, 17.2% and 4.4% were due to Na(+), HCO(3)(-), SO(4)(--), NO(3)(-) and Ca(++)+ Mg(++). The analysis shows that a good correlation exists between EC, Cl(-) and SO(4)(--) either individually or in combination with other ions and the multiple regression models can predict EC at 5% level of significance.     

Atmospheric deposition of major ions and trace metals near an industrial area,Jordan

Al, Cd, Cr, Cu, Fe, Mn, Pb, Zn, NH4+, Mg2+, Ca2+, Na+, K+, Cl-, NO3- and SO4(2-), along with pH were determined in wet and dry deposition samples collected at Al-Hashimya, Jordan. Mean trace metal concentrations were similar or less than those reported for other urban regions worldwide, while concentrations of Ca2+ and SO4(2-) were the highest. The high Ca2+ concentrations were attributed to the calcareous nature of the local soil and to the influence of the Saharan dust, while the high concentrations of SO4(2-) were attributed to the influence of anthropogenic sources and Saharan dust soil. Except for SO4(2-), NO3-, and Ca2+, dry deposition fluxes of measured metals and ions were higher than their corresponding wet deposition fluxes. The high annual average pH values recorded for wet and dry deposition samples were attributed to the neutralization of acidity by alkaline species. Cd, Cr, Cu, Pb, Zn, NO3- and SO4(2-) were enriched in wet and dry deposition samples relative to crustal material, and a significant anthropogenic contribution to these elements and ions is tentatively suggested. Finally, the possible sources and the main factors affecting the concentrations of the measured species are discussed.     

An application of multivariate analysis to acid rain data in Northern Italy to discriminate natural and man-made compounds

This paper presents the preliminary results of a study, the aim of which was to analyse the pluviometric and chemical rain data, recorded by a wet only network located in Northern Italy.More in detail, precipitations were collected on a weekly basis and chemical analysis was performed on pH, electric conductivity and Ca, Mg, Na, K, NH₄, NO₃, SO₄, Cl concentrations.The Principal Components Analysis pointed out that the first three components are enough to explain more than 90% of the variability of the parameters. Moreover each component may have a different physical interpretation, that is the first one is mainly related to the precipitation amount, while the second to the man made and natural sources and the last one to the sea/soil contribution.     

Chemical characterization of precipitation at a coastal site in Trombay, Mumbai, India

Precipitation is the best scavenger for the particulates and dissolved gaseous pollutants present in the atmosphere. The chemical composition of precipitation is dominated by a number of in-cloud and below-cloud scavenging processes. The present study is aimed at analyzing the chemical composition of rainwater in the relatively less industrialized part of Mumbai. The pH of rainwater in this region ranges from 4.8 to 6.4. The percentage contributions of ions were calculated and the major contributing ions were calcium (28%), chloride (23%), sodium (18%), sulfate (14%), magnesium (11%), ammonium (4%), potassium (1%), and nitrate (1%). The correlation coefficient is highest for Na and Cl (r ²?=?0.99), giving a clear indication of contribution from sea salt. Sulfate and nitrate ions also show a very good correlation (r ²?=?0.90), which may be due to their coemission from fossil fuel combustion. Acidification caused by these ions is neutralized by Ca, Mg, and NH₄ ions. The neutralization effect due to these ions is validated by calculating the neutralization factor (NF). The NF values are in the order Ca > Mg > NH₄. The major source contributors for the ions in precipitation are sea salt (Na, Cl, and K) and fossil fuel combustion (SO₄ and NO₃). These assumptions are supported by the values of wet-only ratio, enrichment factor, and percent sea salt fraction.     

2009—2017年南充市城区酸雨特征分析

为了更为有效地治理酸雨污染,根据南充市环境监测中心站提供的2009—2017年降水监测数据,对南充市城区酸雨污染情况进行了分析及源解析。结果表明:2009—2017年,南充市降水pH从4.60波动上升至5.6以上,酸雨频率波动下降,酸雨污染情况有所改善;[SO4^2-]/[NO3^-]从4.92下降至0.86,酸雨污染类型从硫酸型转变为硝酸-硫酸型。同时,对比分析2014—2016年大气污染物排放源可知,NOx排放源中,工业污染源占比由14%降至11%,生活污染源由2%上升至5%;SO2排放源中,工业污染源占比由62%降至43%,生活污染源由38%上升至57%,表明南充市SO2污染已从以工业污染源为主转变为工业污染源与生活污染源并重。     

On-site simultaneous determination of anions and cations in drainage water using a flow injection-capillary electrophoresis system with contactless conductivity detection

Drainage water diverted from a farm pasture, which was heavily loaded with manure, was monitored during a rain event. Concurrent anion and cation determinations at intervals of 10 min could be achieved with a new capillary electrophoresis system employing dual injection at opposite ends of the separation capillary. The flow injection approach enabled automation of the sampling process. Interruption of the separation voltage was not necessary. Contactless conductivity detection with an electrolyte solution optimized for the purpose allowed the facile simultaneous detection of the inorganic ions Cl(-), NO(3)(-), SO(4)(2-), HPO(4)(2-), NO(2)(-), NH(4)(+), K(+), Ca(2+), Na(+) and Mg(2+) and the acquisition of temporal concentration profiles of these species. The detection limits achieved were between 20 and 200 [micro sign]g l(-1) for all ions and the repeatability of peak areas and peak heights was better than 1%. The quantitative results were verified by analysing individual samples later in the laboratory with photometry and ion chromatography and the average deviations were found to be between 4 and 12%. This contribution presents a further step in the development of capillary electrophoresis towards a fully automated, low maintenance field method.     

Composition, seasonal variation, and sources of PM10 from world heritage site Taj Mahal, Agra

Air samples for PM(10) (dp?相似文献   

Hydrogeochemical study of shallow carbonate aquifers, Rameswaram Island, India

Groundwater quality assessment has been carried out based on physicochemical parameters (pH, EC, TDS, CO(3), HCO(3), Cl, SO(4), PO(4), NO(2), Ca(+2), Mg(+2), Na(+) and K(+)) and metal concentration in the Rameswaram Island from 25 bore wells. The Langelier Saturation Index of the groundwater shows positive values (63% samples) with a tendency to deposit the CaCO(3) in the majority of water samples. Scatter plot (Ca + Mg/HCO(3)) suggests carbonate weathering process, which is the main contributor of Ca(2+), Mg(2+) and HCO(3) ions to the water. Gibbs diagram suggests rock-water interaction dominance and evaporation dominance which are responsible for the change in the quality of water in the study area. NaCl and mixed CaNaHCO(3) facies are two main hydrogeochemical facies of groundwater. Mathematical calculations and graphical plots of geochemical data reveal that the groundwater of Rameswaram Island is influenced by natural weathering of rocks, anthropogenic activities and seawater intrusion due to over exploitation. Weathering and dissolution of carbonate and gypsum minerals also control the concentration of major ions (Ca(+2), Mg(+2), Na(+) and K(+)) in the groundwater. The nutrient concentration of groundwater is controlled to a large extent by the fertilizers used in agricultural lands and aquaforms. Comparison of geochemical data shows that majority of the groundwater samples are suitable for drinking water and irrigation purposes.     

山西省大气降水水质评价

为了解山西省大气降水水质状况、主要污染物及区域分布规律，山西省水文部门于1984年开始对大气降水进行监测。在全省9个地市布设测点，分别为：太原市、大同市、长治市、榆次市、临汾市以及吕梁、忻州、阳泉、运城地区。监测项目为H^2 、电导率、Ca^2 、Mg^2 、K^2 、Na^2 、NH4^2 、SO4^2-、NO3^-、Cl^-、CO3^-、HCO3^-、F^-。结果表明，除吕梁、忻州地区外。山西省各地市均有酸雨发生，但酸雨发生的频率不高，全省年平均为3．3％；酸雨的酸性程度也不高，对生态可造成明显影响的降水次数不多；山西省酸雨为典型的硫酸型，酸雨中硫酸与硝酸的质量浓度比值远高于全国平均值。     

Precipitation composition and wet deposition temporal pattern in Central Serbia for the period from 1998 to 2004

Bulk samples collected on a daily basis at three principal meteorological stations in central Serbia were analyzed on chloride (Cl(-)), nitrate [Formula: see text], sulfate [Formula: see text], sodium (Na(+)), ammonium [Formula: see text], potassium (K(+)), calcium (Ca(2+)), and magnesium (Mg(2+)) in addition to precipitation amount, pH and conductivity measurements over the period 1998-2004. The data were subjected to variety of analyses (linear regression, principal component analysis, time series analysis) to characterize precipitation chemistry in the study area. The most abundant ion was [Formula: see text] with annual volume weighted mean concentration of 242 microeq L(-1). Neutralization of precipitation acidity occurs both as a result of the dissolution of alkaline compounds containing Ca(2+), Mg(2+), and K(+) as well as the absorption of ammonia. The ratio of [Formula: see text] was above 5, which indicated that the combustion process of low-grade domestic lignite for electricity generation from coal-fired thermal power plants was the main source of pollution in the investigated area. A considerable mean annual bulk wet deposition of SO(4)-S determined by precipitation amount and concentrations of sulfate in the precipitation was calculated to be 12-35 kg ha(-1).     

杭州市酸雨污染现状及成因分析

对杭州市1998年—2002年的降水监测数据进行了统计分析。结果表明,2002年杭州市区酸雨频率为73.6%,降水pH均值为4.68,临安酸雨频率高达97.5%,降水pH均值为4.04,其余几个县(市)降水酸度均<5.60。杭州市有82.1%面积属重酸雨区。指出,杭州市气象条件不利于大气中SO2、NOx的扩散,土壤扬尘不能对酸雨的形成起有效的缓冲作用,因此只有通过调整能源结构,从源头控制煤质(含硫量),严格控制机动车尾气污染,以减少SO2、NOx排放量。     

乌鲁木齐市降水酸度及化学特征的初步研究

降水酸度和离子平衡研究结果表明,乌鲁木齐市降水为非酸性雨,但其PH值有较明显的季节变化,降水中的SO_4~(2-)、Ca~(2+)、和NH_4~+是影响酸度的关键离子,与其他地区相比,乌鲁木齐市降水中的Ca~(2+)浓度是酸雨区(贵阳、重庆)平均值的3.50倍,是非酸雨区(北京、天津)平均值的1.86倍。可见,乌鲁木齐市降水酸度的高低,不仅取决于酸性离子浓度,而且更重要的是取决于碱性离子浓度。     

上海市浦东新区大气降水化学组分及其相关性分析

依据上海市浦东新区2010—2015年2个代表性采样点的142份监测数据,对降水中的化学组成及各组分间的相关性进行了分析。结果表明,监测期间单次降雨的pH值为3.85~6.09,平均值为5.09,属硫酸型/硝酸型复合污染酸雨。其中SO_4~(2-)和NO_3~-为主要离子,平均值分别为4.55和3.31 mg/L。通过SPSS统计分析得出,人类生活和生产过程以及海洋源是浦东新区大气降水化学组分的主要来源,但仍存在不同的区域特征。     

Characterization of ionic composition of TSP and PM10 during the Middle Eastern Dust (MED) storms in Ahvaz, Iran

Because of the recent frequent observations of major dust storms in southwestern cities in Iran such as Ahvaz, and the importance of the ionic composition of particulate matters regarding their health effects, source apportionment, etc., the present work was conducted aiming at characterizing the ionic composition of total suspended particles (TSP) and particles on the order of ～10?μm or less (PM(10)) during dust storms in Ahvaz in April-September 2010. TSP and PM(10) samples were collected and their ionic compositions were determined using an ion chromatography. Mean concentrations of TSP and PM(10) were 1,481.5 and 1,072.9?μg/m(3), respectively. Particle concentrations during the Middle Eastern Dust (MED) days were up to four times higher than those in normal days. Ionic components contributed to only 9.5% and 11.3% of the total mass of TSP and PM(10), respectively. Crustal ions were most abundant during dust days, while secondary ions were dominant during non-dust days. Ca(2+)/Na(+) and Cl(-)/Na(+) ratios can be considered as the indicators for identification of the MED occurrence. It was found that possible chemical forms of NaCl, (NH(4))(2)SO(4), KCl, K(2)SO(4), CaCl(2), Ca(NO(3))(2), and CaSO(4) may exist in TSP. Correlation between the anionic and cationic components suggests slight anion and cation deficiencies in TSP and PM(10) samples, though the deficiencies were negligible.     

MULTI-MEDIA CONCENTRATIONS OF HEAVY METALS AND MAJOR IONS FROM URBAN AND RURAL SITES IN NEW BRUNSWICK, CANADA

Concentrations of heavy metals and major ions were measured in precipitation, snowpack, garden soils and vegetables from urban and rural sites in New Brunswick in Atlantic Canada. Atmospheric loading of mercury, lead, cadmium, arsenic, strontium, and vanadium need further assessment. Vanadium concentrations in precipitation, snowpack, soils and vegetables showed an urban influence. Vanadium concentrations in the snowpack ranged between <2.0 ppb at 50 kilometers from the city center to 31.4 ppb in the city. Concentrations of all heavy metals in urban soils were less than CCME remediation guidelines but selected metals exceeded the assessment benchmark non-regulatory guidelines. Major ions were consistently higher in event precipitation than the snowpack. The order of ion elution from the snowpack was NO3 > SO4 > NH4 > H > Mg > Cl > Na > K. Hydrogen ion equivalents were highest in the snowpack and precipitation from urban samples. Mean hydrogen ion concentrations ranged from 11 to 22 eq L-1 in the snowpack compared with 18 to 41 eq L-1 in event precipitation.     

Atmospheric aerosol concentration level and chemical characteristics of water-soluble ionic species in wintertime in Beijing,China

Total suspended particulate (TSP) samples were collected during wintertime from November 24, 1998 to February 12, 1999 in Beijing. Ionic species including Cl-, NO3(-), SO4(2-), Na+, NH4(+), K+, Mg2+ and Ca2+ were determined by Ion Chromatography (IC). The sum average concentration of all the determined ions accounted for 18.9% of the TSP concentration, and SO4(2-) appeared the dominant ion with an average concentration of 30.84 microg m(-3); the sum mass concentration of SO4(2-), NO3(-), Ca2+ and NH4(+) accounted for about 83.2% of all the eight ions measured. The study indicated that the chemical form of sulfate and ammonium varies with TSP concentration levels. During heavy pollution periods, the average TSP concentration was 0.66 mg m(-3), and the NH4(+)/SO4(2-) molar ratio was low (0.58). It indicated that sulfate may present as CaSO4 and (NH4)2SO4 x CaSO4 x 2H2O. When TSP concentration (average 0.186 mg m(-3)) was relatively low, the NH4(+)/SO4(2-) molar ratio was 1.94, close to the theoretical ratio of 2 of (NH4)2SO4. Under this condition (NH4)2SO4 is expected to exist as the major form of sulfate. When the TSP concentration level was medium (average 0.35 mg m(-3)), the NH4+/SO4(2-) molar ratio appeared an average value (1.27), (NH4)2SO4, (NH4)2SO4 x CaSO4 x 2H2O and CaSO4 are expected to be present in those aerosol particles. Meteorological conditions including wind speed and wind direction were related to the TSP concentration level.     

Characterization and diurnal variation of size-resolved inorganic water-soluble ions at a rural background site

Water-soluble inorganic ions in aerosol samples have been studied. The sample collection took place during summer in 2003 at a European background site which is operating within the framework of the European Monitoring and Evaluation Program. Gent type PM10 stacked filter unit (SFU) samplers were operated in parallel on a day and night basis to collect particles in separate coarse (2.0-10 microm) and fine (<2.0 microm) size fractions. Particulate masses were measured gravimetrically; the filters from one of the SFU samplers were analyzed by particle-induced X-ray emission spectrometry (PIXE) and instrumental neutron activation analysis (INAA). Filters from the other SFU sampler were analyzed by ion chromatography (IC) for major inorganic anions (MSA-, NO2(-), NO3(-), Cl-, Br-, SO4(2-), oxalate) and cations (Na+, K+, NH4(+), Mg2+, Ca2+). The water-soluble inorganic ions measured were responsible for 44% and 16% of the total fine and coarse particulate mass, respectively. In the fine size fraction, the main ionic components were SO4(2-) and NH4(+) accounting for about 90% of fine ionic mass. In the coarse fraction the main ionic components were Ca2+ and NO3(-), followed by SO4(2-). Significant day and night difference in the mass concentrations was observed only for fine NO3(-). The molar ratios of fine NH4(+) to SO4(2-) indicated their complete neutralization to (NH4)2SO4. According to the cation-to-anion ratios the coarse particles were alkaline, while the fine particles were slightly acidic or neutral. By comparing the corresponding concentrations obtained from PIXE/INAA and IC, we determined the water-extractable part of the individual species. We also investigated the effect of long-range transported air masses on the local air concentrations, and we found that the air quality of this background monitoring station was affected by regional pollution sources.     

Groundwater quality assessment in the village of Lutfullapur Nawada, Loni, District Ghaziabad, Uttar Pradesh, India

The groundwater quality for drinking, domestic and irrigation in the village Lutfullapur Nawada, Loni, district Ghaziabad, U.P., India, has been assessed. Groundwater samples were collected, processed and analyzed for temperature, pH, conductivity, salinity, total alkalinity, carbonate alkalinity, bicarbonate alkalinity, total hardness, calcium hardness, magnesium hardness, total solids, total dissolved solids, total suspended solids, nitrate-nitrogen, chloride, fluoride, sulfate, phosphate, silica, sodium, potassium, calcium, magnesium, total chromium, cadmium, copper, iron, nickel, lead and zinc. A number of groundwater samples showed levels of electrical conductivity (EC), alkalinity, chloride, calcium, sodium, potassium and iron exceeding their permissible limits. Except iron, the other metals (Cr, Cd, Cu, Ni, Pb, and Zn) were analyzed below the permissible limits. The correlation matrices for 28 variables were performed. EC, salinity, TS and TDS had significant positive correlations among themselves and also with NO (3) (-) , Cl(-), alkalinity, Na(+), K(+), and Ca(2+). Fluoride was not significantly correlated with any of the parameters. NO (3) (-) was significantly positively correlated with Cl(-), alkalinity, Na(+), K(+) and Ca(2+). Chloride also correlated significantly with alkalinity, Na(+), K(+) and Ca(2+). Sodium showed a strong and positive correlation with K(+) and Ca(2+). pH was negatively correlated with most of the physicochemical parameters. This groundwater is classified as a normal sulfate and chloride type. Base-exchange indices classified 73% of the groundwater sources as the Na(+)-SO (4) (2-) type. The meteoric genesis indices demonstrated that 67% of groundwater sources belong to a deep meteoric water percolation type. Hydrochemical groundwater evaluations revealed that most of the groundwaters belong to the Na(+)-K(+)-Cl(-)-SO (4) (2-) type followed by Na(+)-K(+)-HCO (3) (-) type. Salinity, chlorinity and SAR indices indicated that majority of groundwater samples can be considered suitable for irrigation purposes.