Chemical trends in background air quality and the ionic composition of precipitation for the period 1980-2004 from samples collected at Valentia Observatory, Co. Kerry, Ireland

A major Irish study, based upon more than 8000 samples collected over the measurement period of 22 years, for sulfur dioxide (SO2-S), sulfate (SO4-S) and nitrogen dioxide (NO2-N) concentrations (microg m(-3)) within air, and the ionic composition of precipitation samples based on sodium (Na+), potassium (K+), magnesium (Mg2+), calcium (Ca2+), chloride (Cl-), sulfate (SO4-S), non-sea salt sulfate (nssSO4-S), ammonium (NH4-N), and nitrate (NO3-N) weighted mean concentrations (mg l(-1)), has been completed. For the air samples, the sulfur dioxide and sulfate concentrations decreased over the sampling period (1980-2004) by 75% and 45%, respectively, whereas no significant trend was observed for nitrogen dioxide. The highest concentrations for sulfur dioxide, sulfate and nitrogen dioxide were associated with wind originating from the easterly and northeasterly directions i.e. those influenced by Irish and European sources. The lowest concentrations were associated with the westerly directions i.e. for air masses originating in the North Atlantic region. This was further verified with the use of backward (back) trajectory analysis, which allowed tracing the movement of air parcels using the European Centre for Medium range Weather Forecasting (ECMWF) ERA-40 re-analysis data. High non-sea salt sulfate levels were being associated with air masses originating from Europe (easterlies) with lower levels from the Atlantic (westerlies). With the precipitation data, analysis of the non-sea salt sulfate concentrations showed a decrease by 47% since the measurements commenced.     

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).     

A Preliminary Assessment of the Montréal Process Indicators of Air Pollution for the United States

Air pollutants pose a risk to forest health and vitality in the United States. Here we present the major findings from a national scale air pollution assessment that is part of the United States' 2003 Report on Sustainable Forests. We examine trends and the percent forest subjected to specific levels of ozone and wet deposition of sulfate, nitrate, and ammonium. Results are reported by Resource Planning Act (RPA) reporting region and integrated by forest type using multivariate clustering. Estimates of sulfate deposition for forested areas had decreasing trends (1994-2000) across RPA regions that were statistically significant for North and South RPA regions. Nitrate deposition rates were relatively constant for the 1994 to 2000 period, but the South RPA region had a statistically decreasing trend. The North and South RPA regions experienced the highest ammonium deposition rates and showed slightly decreasing trends. Ozone concentrations were highest in portions of the Pacific Coast RPA region and relatively high across much of the South RPA region. Both the South and Rocky Mountain RPA regions had an increasing trend in ozone exposure. Ozone-induced foliar injury to sensitive species was recorded in all regions except for the Rocky Mountain region. The multivariate analysis showed that the oak-hickory and loblolly-shortleaf pine forest types were generally exposed to more air pollution than other forest types, and the redwood, western white pine, and larch forest types were generally exposed to less. These findings offer a new approach to national air pollution assessments and are intended to help focus research and planning initiatives related to air pollution and forest health.     

Evaluating PM₂.₅ ionic components and source apportionment in Jinan, China from 2004 to 2008 using trajectory statistical methods

The mass concentrations and major chemical components of PM(2.5) in Jinan, Shandong Province, China from Dec. 2004 to Oct. 2008 were analyzed using backward trajectory cluster analysis in conjunction with the potential source contribution function (PSCF) model. The aim of this work was to study the inter-annual variations of mass concentrations and major chemical components of PM(2.5), evaluate the air mass flow patterns and identify the potential local and regional source areas that contributed to secondary sulfate and nitrate in PM(2.5) in Jinan. The annual mean concentrations of PM(2.5), sulfate and nitrate in 2004-2008 were almost the highest in the world. The most significant air parcels contributing to the highest mean concentrations of mass and secondary ions in PM(2.5) originated from the industrialized areas of Shandong Province. Clusters with a lower ratio of NO(3)(-)/SO(4)(2-) in PM(2.5) originated from the Yellow Sea, while a higher ratio was observed in the clusters passing through Beijing and Tianjin. PSCF modeling indicated that the provinces of Shandong, Henan, Jiangsu, Anhui and the Yellow Sea were the major potential source regions for sulfate, in agreement with the cluster analysis results. Regional and long-range transport of NH(4)NO(3) played an important role in the nitrate concentration of Jinan. By comparing the distributions of secondary sulfate and nitrate over three years, enhanced emission control management before and during the 29(th) Olympic Games led to a discernible decrease in source contributions from Beijing and its environs in 2007-2008.     

Improved mapping of National Atmospheric Deposition Program wet-deposition in complex terrain using PRISM-gridded data sets

High-elevation regions in the United States lack detailed atmospheric wet-deposition data. The National Atmospheric Deposition Program/National Trends Network (NADP/NTN) measures and reports precipitation amounts and chemical constituent concentration and deposition data for the United States on annual isopleth maps using inverse distance weighted (IDW) interpolation methods. This interpolation for unsampled areas does not account for topographic influences. Therefore, NADP/NTN isopleth maps lack detail and potentially underestimate wet deposition in high-elevation regions. The NADP/NTN wet-deposition maps may be improved using precipitation grids generated by other networks. The Parameter-elevation Regressions on Independent Slopes Model (PRISM) produces digital grids of precipitation estimates from many precipitation-monitoring networks and incorporates influences of topographical and geographical features. Because NADP/NTN ion concentrations do not vary with elevation as much as precipitation depths, PRISM is used with unadjusted NADP/NTN data in this paper to calculate ion wet deposition in complex terrain to yield more accurate and detailed isopleth deposition maps in complex terrain. PRISM precipitation estimates generally exceed NADP/NTN precipitation estimates for coastal and mountainous regions in the western United States. NADP/NTN precipitation estimates generally exceed PRISM precipitation estimates for leeward mountainous regions in Washington, Oregon, and Nevada, where abrupt changes in precipitation depths induced by topography are not depicted by IDW interpolation. PRISM-based deposition estimates for nitrate can exceed NADP/NTN estimates by more than 100% for mountainous regions in the western United States.     

Airborne sulfur and nitrogen in Finland-trends and exposure in relation to air transport sector

We present the concentration trends and the atmospheric exposure of sulfur and nitrogen compounds in different transport sectors during the period 1981-2000, based on the air quality data of the Finnish Meteorological Institute. Sulfur and nitrogen concentrations in air and precipitation were assessed from background stations covering the whole country. A significant decrease of more than 60% was observed in the concentrations of all sulfur compounds throughout the country during 1981-2000. In the 1990's, significant trends were detected in all sulfur time series, with the exception of sulfate in precipitation at the northernmost stations. On the other hand, the concentrations of oxidized nitrogen compounds in air and precipitation have declined only slightly or not at all, especially in the 1990's. This is attributed to the fairly small domestic and European NO(x) emission reductions after 1981. The ammonium concentration in precipitation has declined by more than 50% during 1981-2000. The atmospheric sulfur exposure was found to be dominated by transport from the West and South-West sectors during summer, whereas in winter all the southward sectors were important. The largest decline in the sectoral sulfur concentrations has taken place already before 1991, with a more pronounced reduction during winter than during summer. The atmospheric nitrogen exposure was mainly dominated by transport from the sectors between west and south, but in the latter half of the study period there seems to have been a slight shift towards increased transport from the eastern and northern sectors.     

2003—2018年全国酸雨状况变化趋势研究

基于2003—2018年全国291个城市降水监测结果的分析表明:全国降水酸度明显降低,其中,2003—2006年有所升高,2006年之后呈降低趋势；酸雨区面积呈减小趋势,共减少约97万km²,酸雨发生频率超过5%的面积减少了20.9个百分点；全国酸雨城市比例为21.3%～40.9%,2009年开始总体呈下降趋势,2018年降为21.6%,重酸雨城市比例在2005年之后总体呈下降趋势；全国平均酸雨频率为11.7%～25.6%,2006年之后总体呈下降趋势,2018年酸雨频率在50%以上的城市比例较2006年下降了13.9个百分点。基于174个城市的降水离子组分分析结果显示:我国降水中的主要阴离子为硫酸根,其离子当量浓度占比为19.4%～32.9%,2003年以来年平均降低0.6个百分点；降水中的主要阳离子为钙离子和铵离子；硫酸根沉降通量年平均下降0.68 t/km²,硝酸根沉降通量年平均降低0.05 t/km²,全国SO₂浓度变化趋势与硫酸根沉降通量变化趋势基本一致；我国降水中的硝酸根与硫酸根离子当量浓度比值总体呈升高趋势,表明硝酸根离子对降水酸度的影响逐渐增加,酸雨类型正由硫酸型向硫酸-硝酸混合型转变。     

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.     

Atmospheric wet deposition of soluble macro-nutrients in the Cilician Basin, north-eastern Mediterranean sea

In order to estimate wet deposition atmospheric fluxes of macro-nutrients into the eastern Mediterranean coastal waters, soluble inorganic phosphate (PO4(3-)), nitrate (NO3-) and nitrite (NO2-) concentrations in precipitation (from February 1996 to June 1997) have been measured at a coastal sampling site, Erdemli, Turkey. Water-soluble inorganic PO4(3)-P, a reactive, bioavailable, limiting macro-nutrient in the oligotrophic waters of the eastern Mediterranean was studied with respect to its contribution to biological productivity. Reactive PO4(3-)-P and NO2(-) + NO3(-)-N concentrations were found to be highly variable in rainwater samples. One of the aims of the study was to determine the contribution of dust transport to the soluble macro-nutrient budget of the eastern Mediterranean. No differences were found between the mean reactive P and NO(2-) + NO3(-)-N concentrations of "red rain" and normal rain events. Most likely as a result of low solubility of crustal phosphorus, dust episodes were not found to be important sources of reactive P, in terms of wet deposition. The annual wet deposition fluxes of reactive PO4(3-)-P and NO2(-) + NO3(-)-N into the Cilician Basin were respectively estimated to be 0.010 g P m(-2) per year and 0.23 g N m(-2) per year, which are comparable to the fluxes from land-based sources in the north-eastern Mediterranean. The incorporation of water soluble bioavailable PO4(3-)-P and NO2(-) + NO3(-)-N delivered via atmospheric wet deposition could be responsible for approximately 3.3% (0.40 g C m(-2) per year) and 11.0% (1.31 g C m(-2) per year) respectively, of the mean annual new production in the north-eastern Mediterranean.     

Analysis of Wet Precipitation of Air Pollutants in Mumbai (India)

Bulk precipitation samples at Mumbai (India) were collectedduring the monsoon seasons of 1991 to 1996 and analysed forionic concentrations using an Ion Chromatograph DIONEX model100. The variability of sulphate to nitrate ratio in rainwaterfluctuates in a wide range from 1.5 to 20 and governed by thesulphate concentrations in the sample. The regression analysisof the data reveals that in the bulk precipitation at Mumbai, SO₄ ^2- is becoming increasingly important relative toNO₃ ^-. The role of meteorological influences onscavenging of air pollutants by rain water has been tried toexplain the phenomena. The computed wet deposition rates for Sand N during 1991–1996 show that the S deposition is higherthan N in all the years. There is a wide fluctuation indeposition rates of S ranging from 2 to 55 kg km² per annum.     

Particle emission from heavy-duty engine fuelled with blended diesel and biodiesel

In this study, particulate matter (PM) were characterized from a place impacted by heavy-duty vehicles (Bus Station) fuelled with diesel/biodiesel fuel blend (B3) in the city of Londrina, Brazil. Sixteen priority polycyclic aromatic hydrocarbons (PAH) concentrations were analyzed in the samples by their association with atmospheric PM, mass size distributions and major ions (fluorite, chloride, bromide, nitrate, phosphate, sulfate, nitrite, oxalate; fumarate, formate, succinate and acetate; lithium, sodium, potassium, magnesium, calcium and ammonium). Results indicate that major ions represented 21.2% particulate matter mass. Nitrate, sulfate, and ammonium, respectively, presented the highest concentration levels, indicating that biodiesel may also be a significant source for these ions, especially nitrate. Dibenzo[a,h]anthracene and indeno[1,2,3,-cd]pyrene were the main PAH found, and a higher fraction of PAH particles was found in diameters lower than 0.25 μm in Londrina bus station. The fine and ultrafine particles were dominant among the PM evaluated, suggesting that biodiesel decreases the total PAH emission. However, it does also increase the fraction of fine and ultrafine particles when compared to diesel.     

Indoor air quality during renovation actions: a case study

A temporary renovation activity releases considerably high concentrations of particulate matter, viable and non-viable, into air. These pollutants are a potential contributor to unacceptable indoor air quality (IAQ). Particulate matter and its constituents lead, sulfate, nitrate, chloride, ammonium and fungi as well as fungal spores in air were evaluated in a building during renovation action. Suspended dust was recorded at a mean value of 6.1 mg m(-3) which exceeded the Egyptian limit values for indoor air (0.15 mg m(-3)) and occupational environments (5 mg m(-3)). The highest particle frequency (23%) of aerodynamic diameter (dae) was 1.7 microm. Particulate sulfate (SO(4)(2-)), nitrate (NO(3)(-)), chloride (Cl(-)), ammonium (NH(4)(+)) and lead components of suspended dust averaged 2960, 28, 1350, 100 and 13.3 microg m(-3), respectively. Viable fungi associated with suspended dust and that in air averaged 1.11 x 10(6) colony forming unit per gram (cfu g(-1)) and 92 colony forming unit per plate per hour (cfu p(-1) h(-1)), respectively. Cladosporium(33%), Aspergillus(25.6%), Alternaria(11.2%) and Penicillium(6.6%) were the most frequent fungal genera in air, whereas Aspergillus(56.8%), Penicillium(10.3%) and Eurotium(10.3%) were the most common fungal genera associated with suspended dust. The detection of Aureobasidium, Epicoccum, Exophiala, Paecilomyces, Scopulariopsis, Ulocladium and Trichoderma is an indication of moisture-damaged building materials. Alternaria, Aureobasidium, Cladosporium, Scopulariopsis and Nigrospora have dae > 5 microm whereas Aspergillus, Penicillium and Verticillium have dae < 5 microm which are suited to penetrate deeply into lungs. Particulate matter from the working area infiltrates the occupied zones if precautionary measures are inadequate. This may cause deterioration of IAQ, discomfort and acute health problems. Renovation should be carefully designed and managed, in order to minimize degradation of the indoor and outdoor air quality.     

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.     

长江入海口北岸单站降水组分10年变化状况探讨

分析2001—2010年南通市区城中子站降水监测点位数据,得出降水中起致酸作用的阴离子硫酸根、硝酸根、氟离子和氯离子中除硝酸根呈现显著性上升趋势,其余上升趋势不明显;氯离子、钠离子与降水量存在高度线性负相关,硫酸根、硝酸根与降水量分别为低度非线性负相关和正相关,其他项目与降水量为显著性非线性负相关;将pH分5级,pH<4.7为重酸雨频率,pH4.7～5.0为较重酸雨频率,pH5.0～5.3为中度酸雨频率,pH5.3～5.6为轻度酸雨频率,pH≥0.56为非酸雨频率,其结果表明:南通市区2009、2010年酸雨频率降低,分别为44.1%和38.2%,主要是重酸雨频率减少,非酸雨频率增加;2003、2007年酸雨频率升高,分别为67.4%和69.8%,主要是重酸雨频率增加,非酸雨频率减小;降水量大小与电导率浓度高低没有对应性;阴阳离子浓度总量逐年、逐月同步变化;阴离子中硫酸根、硝酸根浓度逐年、逐月变化量与幅度较大;阳离子中钙离子、铵离子浓度逐年、逐月变化量与幅度较大;阴阳离子浓度逐年、逐月占比呈准对称形。     

Nitrate Leaching by Atmospheric N Deposition to Upper Groundwater in the Sandy Regions of The Netherlands in 1990

Anthropogenic increase in atmospheric nitrogen (N) deposition in nature areas results in nitrate leaching to groundwater, threatening its quality. Member states of the European Union are obliged to reduce groundwater nitrate concentrations and to monitor this reduction. The relationship between N deposition and groundwater nitrate concentrations is quantified using a field survey and geographical information. Nitrate concentrations of the uppermost metre of groundwater in nature areas in the sandy regions in 1990 were related to geographical data by means of regression analysis. In this way nitrate concentrations could be explained by potential ammonia deposition, soil type, vegetation and land use. We found that about 35% of 54 kg ha(-1) a(-1) atmospheric N deposition was leached to the upper groundwater as nitrate, resulting in a mean NO3 concentration of about 30 mg L(-1). The critical N load for exceeding the EC limit value (50 mg L(-1)) in the sandy regions of The Netherlands composed of natural vegetation will be about 80 kg ha(-1) a(-1). Leaching is less than expected for nature areas but comparable with leaching of N surpluses in pastures in The Netherlands. A reduction in nitrate leaching by 25% or more can currently be detected via a new field survey.     

A Global Overview of Atmospheric Acid Deposition Fluxes

This paper presents a summary of globalacid deposition flux data taken from a globalassessment report on acid deposition prepared forUNEP/WMO (Whelpdale and Kaiser, 1996). There is a largevariation in the spacial coverage and reliability ofmonitoring around the world. Many more stationsmeasure wet deposition than collect appropriate datafor estimating dry deposition. The widespread regionswith highest precipitation concentrations anddeposition fluxes of sulphate and nitrate coincideclosely with the regions of highest density ofSO₂ and NO_x precursor emissions occurringprimarily in the mid-latitude, northern hemispherebelt where a large fraction of the worlds fossilfuels is consumed. Organic acids in precipitation makea minor contribution to acidity (<20%) inindustrial regions, but in the rest of the world theyare of same order, or even exceed, inorganic acids.Less is known about dry deposition, but it appears topredominate near strong emission sources with wetdeposition predominating farther downwind. The molarratio of the N/S contribution to acidic deposition isclose to 1.0 over large areas of Europe and NorthAmerica, but is highly variable elsewhere, beinghighest in equatorial regions due to biomass burningand lowest near smelters and other large sources of SO₂.     

Evaluation of filter-based aerosol measurements during the 1987 Southern California Air Quality Study

The Southern California Air Quality Study (SCAQS) was conducted during the summer and fall of 1987 to assess the causes of elevated ozone and suspended particulate matter concentrations in California's South Coast Air Basin (SoCAB). Extensive gaseous (i.e. nitric acid, ammonia, sulfur dioxide) and particle (i.e. PM_2.5 and PM₁₀ mass, elements, ions, carbon) measurements were acquired for 11 days during the summer at nine locations, and six days during the fall at six locations. Outliers were identified so that they could be excluded from further statistical analyses. Carbon and elemental measurements were found to be negatively biased by 20% owing to inhomogenous aerosol deposits on the SCAQS filters and analysis methods which were applied to a portion of the filters. These biases seem relatively consistent, however, and should not affect conclusions drawn from data analysis efforts if they are appropriately considered. Significant fractions (30–60%) of ammonium nitrate volatilized during the summer when temperatures were higher. Less than 10% typically volatilized during the fall when temperatures were lower. Anion/cation balances support the accuracy and precision estimates of the nitrate, sulfate, and ammonium measurements. Coarse particle sulfate was generally low, while coarse particle nitrate was most pronounced at the coastal sites.This paper documents SCAQS filter-based aerosol measurement methods, and evaluates the accuracy, precision, and validity of the data set. Various comparisons were made for: (1) PM_2.5/PM₁₀ ratios for mass and major chemical species; (2) sum of chemical species versus measured mass; (3) sulfate versus sulfur ratios; (4) PM_2.5 particulate nitrate versus nitric acid-denuded nitrate; and (5) anion/cation balances. The measurement and evaluation techniques presented in this paper serve as a guideline for other data analysis and modeling studies.     

降雨对长三角区域PM2.5浓度的影响

利用WRF-CAMx模式分析首届中国国际进口博览会(简称进博会)期间一次降雨过程对长三角地区PM2.5浓度影响,结果表明,降雨量分布区域与因降雨造成的PM2.5浓度减少量分布区域并不完全一致,湿沉降量受降雨量、PM2.5浓度和风速等多个因素共同影响。数值模拟结果表明,降雨导致浓度下降幅度排前5位的组分分别是有机气溶胶、硫酸盐、硝酸盐、铵盐和细颗粒原生气溶胶,下降幅度分别为44. 28%、16. 55%、11. 55%、9. 53%和5. 23%。结合观测资料和数值模式模拟结果可知,首届进博会期间上海本地减排和周边区域协同控制作用使PM2.5日均质量浓度降低33. 23μg/m3,因降雨引起的湿沉降作用使上海市PM2.5质量浓度降低15. 88μg/m^3。     

金华市大气降水的化学组成特征及来源解析

对2004年大气降水样品监测资料的综合分析和研究表明,金华市降水样品pH值的分布范围在3.64~6.76之间,降水的酸雨率为79.3%。SO24-和NO-3是降水中主要的阴离子,分别占降水中阴离子总量的66.1%和21.7%。NH 4和Ca2 是降水中含量最高的阳离子,分别占阴离子总量的56.6%和33.4%。降水中这些离子的浓度水平一般比世界上其它地方高,但大大低于国内的北方地区。由于降水中缺乏足够的中和物质,大约76%的降水酸度被NH 4、Ca2 和K 等碱性成分中和。陆源型离子Ca2 、Mg2 和K 以及海盐性离子Na 和Cl-之间存在明显的相关关系,另外Ca2 和SO24-、Mg2 和SO24-、Mg2 和NO-3以及Mg2 和Cl-之间也可以观察到比较好的相关关系。土壤和海水的富集系数表明,研究区域的Ca2 和K 主要来源于岩石/土壤风化,SO24-和NO-3主要归因于人为活动的影响。     

A comparison of European and North American atmospheric deposition networks: polycyclic aromatic hydrocarbons and lindane

A comparison between the sampling and analytical methods used by Canadian (IADN) and German (OSPAR) regional monitoring networks for persistent organic pollutants was conducted from September 2002 to October 2003 at a rural site in Ontario, Canada. Polycyclic aromatic hydrocarbons (PAHs) and the currently-used pesticide lindane were measured in precipitation and ambient air samples. Overall the two networks sampling and analytical methods agreed well in their results of deposition (wet and dry particulate). Lindane concentrations between the two networks agreed well in the air samples while too few precipitation samples could be compared to conclude on agreement. The lindane seasonal profile with a peak in spring-early summer was consistent with previous results pointing to the continued use of this pesticide in 2002-2003 in Canada. Annual lindane wet depositions were comparable between the two network methodologies. PAHs concentrations in precipitation and in gas phase agreed well while there was a discrepancy for particulate PAHs in air. This study confirmed that the use of data from the two regional POPs monitoring networks for hemispherical modelling studies is warranted.