Estimation of Ammonia Emission in South Korea

The importance of ammonia (NH₃) in the atmosphere andits role in acidification is increasingly recognized. Adetailed emission inventory of NH₃ for South Korea iscarried out for different sources using emission factors.Results indicate that the emission of ammonia has increasedby 21% over the last 11 yr from 143 000 t yr^-1 in1988 to 181 000 t yr^-1 in 1998. The major contributorsto the NH₃ emission in South Korea are livestock andfertilizer application that account for 70 and 26% oftotal NH₃ emission, respectively. The 11 × 14 km (0.125° long. × 0.125° lat.) grid distribution of emission of ammonia shows an maximum in the Yochon area due to the largest fertilizer factory and relatively wide regions of high NH₃ emission in thenorthwestern part of South Korea due to a great number of livestock. It is found that the nitrogen ratio of wet deposition of NH₄ ⁺ to emission of NH₃ in SouthKorea is averaged to be 0.45.     

Estimation and Mapping of Nitrogen Uptake by Forest in South Korea

Regional air pollution in northeast Asia is an emerging environmental problem requiring long-term impact assessment of acidic deposition. In this study, the gridded distribution of nitrogen uptake led by both growing forests and harvested biomass for eight tree species: Japanese Larch, Red pine, Korean pine, Oak tree, Chestnut, Other Conifers, Other broad leaved trees, and Mixed forest was identified to estimate critical loads for nitrogen over South Korea. The gridded spatial distribution of averaged nitrogen uptake was mapped by 0.125° Latitude × 0.125° Longitude resolution. The results showed that net uptake of nitrogen led by both growth and harvested biomass was totaled at 438 mol_c ha^?1 year^?1 among which harvested biomass contribution was estimated to be 25 mol_c ha^?1 year^?1, yielding a very small fraction of total nitrogen uptake presumably due to the younger stages of forest in South Korea.     

Estimation of the Maximum Critical Load for Sulfur in South Korea

The maximum critical load of sulfur and its exceedance by the sulfur deposition of 1994–1997 were mapped for South Korea with a spatial resolution of 11 × 14 km using the steady-state mass balance method. The Korean soil and geological maps were used as basis for the estimations of the critical alkalinity leaching and the weathering rate of base cations. The normalized difference vegetation index data obtained from the Advanced Very High Resolution Radiometer (AVHRR) together with the observed primary productivity of plants were used for the estimation of the critical uptake of base cations. Wet deposition of the non-sea-salt base cations was derived from measured base cation concentrations in precipitation, precipitation rate and air concentration of total suspended particulate while dry deposition of base cations was estimated using the inferential technique using scavenging ratios. The predominant ranges of base cation weathering, uptake and deposition were estimated to be of 200 – 600 eq ha^?1 yr^?1, 200 – 400 eq ha^?1 yr^?1 and 400 – 600 eq ha^?1 yr^?1, respectively. Critical alkalinity leaching was mainly in the range of 1000 – 2000 eq ha^?1 yr^?1 due to relatively high value of precipitation runoff. Exceedance of sulfur critical load was found at 40 % of the ecosystems considered mainly in the southeastern part of Korea, and about 60 % of Korea ecosystems were sustainable against sulfur acidity loadings.     

Effects of warming, wetting and nitrogen addition on substrate-induced respiration and temperature sensitivity of heterotrophic respiration in a temperate forest soil

Soil heterotrophic respiration and its temperature sensitivity are affected by various climatic and environmental factors.However,little is known about the combined effects of concurrent climatic and environmental changes,such as climatic warming,changing precipitation regimes,and increasing nitrogen(N)deposition.Therefore,in this study,we investigated the individual and combined effects of warming,wetting,and N addition on soil heterotrophic respiration and temperature sensitivity.We incubated soils collected from a temperate forest in South Korea for 60 d at two temperature levels(15 and 20℃,representing the annual mean temperature of the study site and 5℃warming,respectively),three moisture levels(10%,28%,and 50%water-filled pore space(WFPS),representing dry,moist,and wet conditions,respectively),and two N levels(without N and with N addition equivalent to 50 kg N ha^-1year^-1).On day 30,soils were distributed across five different temperatures(10,15,20,25,and 30℃)for 24 h to determine short-term changes in temperature sensitivity(Q₁₀,change in respiration with 10℃increase in temperature)of soil heterotrophic respiration.After completing the incubation on day 60,we measured substrate-induced respiration(SIR)by adding six labile substrates to the three types of treatments.Wetting treatment(increase from 28%to 50%WFPS)reduced SIR by 40.8%(3.77 to 2.23μg CO₂-C g^-1h^-1),but warming(increase from 15 to 20℃)and N addition increased SIR by 47.7%(3.77 to 5.57μg CO₂-C g^-1h^-1)and 42.0%(3.77 to 5.35μg CO₂-C g^-1h^-1),respectively.A combination of any two treatments did not affect SIR,but the combination of three treatments reduced SIR by 42.4%(3.70 to 2.20μg CO₂-C g^-1h^-1).Wetting treatment increased Q₁₀by 25.0%(2.4 to 3.0).However,warming and N addition reduced Q₁₀by 37.5%(2.4 to 1.5)and 16.7%(2.4 to 2.0),respectively.Warming coupled with wetting did not significantly change Q₁₀,while warming coupled with N addition reduced Q₁₀by 33.3%(2.4 to 1.6).The combination of three treatments increased Q₁₀by 12.5%(2.4 to 2.7).Our results demonstrated that among the three factors,soil moisture is the most important one controlling SIR and Q₁₀.The results suggest that the effect of warming on SIR and Q₁₀can be modified significantly by rainfall variability and elevated N availability.Therefore,this study emphasizes that concurrent climatic and environmental changes,such as increasing rainfall variability and N deposition,should be considered when predicting changes induced by warming in soil respiration and its temperature sensitivity.     

Acid deposition to nature areas in the Netherlands: Part I. Methods and results

In this paper estimates of dry and wet deposition of acidifying substances in the Netherlands are presented. The deposition was estimated from measured concentrations in the atmosphere and in precipitation or if these were not available, from modelled concentrations. The method was applied for the Netherlands on a 5×5 km scale. The most important components are sulphur oxides and ammonia and their reaction products. It was estimated that the annual average deposition of SO _x in the Netherlands decreased from 1570 to 670 mol ha^?1 a^?1 between 1980 and 1989. In 1989, the annual average NO _y deposition was estimated to be 1220 mol ha^?1 a^?1 in 1980 and 1160 mol ha^?1 a^?1 in 1989. The annual average NH _x deposition in the Netherlands was estimated to be 2330 and 2190 mol ha^?1 a^?1 in 1980 and 1989 respectively. HCI deposition was about 100 mol ha^?1 a^?1 in all years. Dry deposition contributes most to the total deposition for each component. The spatial distribution of the total deposition shows a gradient over the Netherlands with highest values in the South and lowest in the North of the country. Meteorological conditions are also of influence on the deposition fluxes for all components. During 1988 and 1989 meteorological conditions favoured low deposition. The estimated uncertainty in the average fluxes of SO _x , NO _y , and NH _x for the Netherlands is 15, 25, and 30% respectively. The wet deposition fluxes can be estimated more accurately than the dry deposition.     

Observed regional distribution of sulfur dioxide in Asia

SO₂ concentrations have been measured for one year at forty-five locations throughout Asia using passive samplers. Duplicate samples were exposed at each site for one month intervals. The sites were selected to provide background information on the distribution of SO₂ over wide geographical regions, with emphasis on the regional characteristics around areas estimated to be sensitive to sulfur deposition. The annual mean values ranged from less than 0.3 μg/m³ at Tana Rata, located at 1545 m on the Malaysia Peninsula, Lawa Mandau, (Borneo) Malaysia, and Dhankuta, Nepal, to values greater than 20 μg/m³ at Luchongguan (Guiyang) China, Babar Mahal, Nepal, and Hanoi, Vietnam. In general high concentrations were measured throughout China, with the highest concentrations in the heavy industrial areas in Guiyang. The concentrations in east Asia around the Korea peninsula were ～5 μg/m³. The concentrations in the southeast Asia tropics were low, with no station in Malaysia and Indonesia having average concentrations exceeding 1.7 μg/m³. The observed SO₂ concentrations were found to display a distinct seasonal cycle which is strongly influenced by the seasonality of winds and precipitation patterns.     

Trends in Sulfate,Base Cations and H+ Concentrations in Bulk Precipitation and Throughfall at Integrated Monitoring Sites in Finland 1989-1995

Temporal trends in sulfate, base cation (Ca2+ + Mg2+ + K+), and H+ ion concentrations in bulk precipitation and throughfall samples collected over a seven year period (1989-95) in four forested catchments in Finland are presented. The catchments are in remote locations and span the boreal zone (61-69 °N). The stands represent old, undisturbed forests, and are composed of varying proportions of Scots pine, Norway spruce and deciduous species (mainly Betula spp.). Monthly SO₄ ^2- and H+ ion concentrations in bulk precipitation averaged over the study period and catchments were: 18.7 µmol L^-1 and 32.3 µmol L^-1. The corresponding values for throughfall were: 37.4 µmol L^-1 and 32.4 µmol L^-1. Sulfate and H+ ion concentrations in bulk precipitation and throughfall both showed negative linear trends, which were significant (p < 0.05) for the three southernmost catchments. Concentrations and trend slope decreased northwards (e.g., bulk precipitation SO₄ ^2- slope estimates: ^-1.6 to ^-1.0 µmol L^-1 yr^-1). The decline was greater for throughfall than for bulk precipitation, indicating a proportionally greater reduction in dry deposition than wet. The sum of base cation concentrations averaged 12.1 µmol(+) L^-1 in bulk precipitation and 83.1 µmol(+) L^-1 in throughfall. There were no significant trends in the sum of base cations (p > 0.05). It is concluded that the reported reduction in S emissions over the study period has resulted in a significant reduction in the acidity and SO₄ ^2- concentration of bulk precipitation, and this reduction has has been reflected in throughfall concentrations. The greatest reduction has taken place in the southern part of the country.     

Estimating the atmospheric input of pollutants into a watershed

Estimating the atmospheric input of ions to a watershed has traditionally been accomplished through either the extrapolation of point measurements of deposition or the integration of model estimated deposition. This paper examines the characteristics of precipitation chemistry on the eastern seaboard of the United States where precipitation quality could conceivably affect fish habitats in estuaries. The measured values presented here have been extracted from the data base of the Utility Acid Precipitation Sampling Program (UAPSP) precipitation chemistry network. These data illustrate the nature of ionic deposition at four points on the eastern seabord. The deposition of H' (acidity) is shown to be dependent upon the amount of sulfate and, to a lesser degree, nitrate in the precipitation. It is also shown that the quantity of ionic deposition on a storm-by-storm basis was influenced by the amount of water deposition but the relationship was not very strong. Thus the use of water deposition as a surrogate for ionic deposition is not justified in these watersheds. Finally, it is shown that the deposition of H⁺, SO₄ ^2?, NO₃ ^?, and NH₄ ⁺ were not clearly seasonal. While a large percentage of total ionic deposition occurred in a small number of precipitation events, these exceptional events were not confined to a particular season.     

Evalution of Acid Deposition in Korea

This study was carried out to evaluate acid depositions and to understand their effect. Wet precipitation has been collected at twenty-four sites in Korea for one year of 1999. The ion concentrations such as H⁺, Na⁺, K⁺, Mg²⁺, NH₄ ⁺, Ca²⁺, Cl^?, NO₃ ^? and SO₄ ^2? were chemically analyzed and determined. Precipitation had wide range of pH(3.5～8.5), and volume-weighted average was 5.2. The contribution amounts of Cl^?, SO₄ ^2? and NO₃ ^? in anion were shown to be 54%, 32%, and 14%, respectively and those of Na⁺ and NH₄ ⁺ in cation were 32% and 25%. The ratios of Cl^? and Mg²⁺ to Na⁺ in precipitation were similar to those of seawater, which imply that great amount of Cl^? and Mg²⁺ in precipitation could be originated from seawater. The concentration of H⁺ is little related with SO₄ ^2?, NO₃ ^? and Cl^? ions, whereas nss^?SO₄ ^2? and NO₃ ^? are highly correlated with NH₄ ⁺, which could suggest that great amount of SO₄ ^2? and NO₃ ^? exist in the form of ammonium associated salt. The annual wet deposition amounts (g m^?2year^?1) of SO₄ ^2?, NO₃ ^?, Cl^?, H⁺, NH₄ ⁺, Na⁺, K⁺, Ca²⁺ and Mg²⁺ were estimated as 0.88～4.89, 0.49～4.37, 0.30～9.80, 0.001～0.031, 0.06～2.15, 0.27～4.27, 0.10～3.81, 0.23～1.59 and 0.03～0.63.     

Physical and Chemical Properties of a Winter-Time Yellow Sand Event in Northeast Asia

The long range transport of mineral dust such as Yellow Sand (YS) is not restricted to the springtime periods in Northeast Asia. A YS phenomenon was observed during 25～27 January 1999, which was a remarkably distinctive episode in the occurrence time and intensity that had ever been observed in the wintertime in Korea. This YS event had a bi-modal temporal structure with the daily average concentrations of 210～349 µg m^?3. The long-lasted second one followed the first arriving short and strong dust pulse. The dominant ion components were SO₄ ^2?, NO₃ ^?, Ca²⁺ and Na⁺ with the concentration of 11.3, 7.6, 6.1 and 4.2 µg m^?3, respectively during the passage of YS, compared to the corresponding concentrations of 4.1, 4.6, 0.4, and 1.2 µg m^?3 after the passage of YS (AYS) over Korea. The mode diameter of these compounds of YS was around 4 µm, compared to 0.4～0.9 µm of AYS. Concentrations of SO₄ ^2? and NO₃ ^? were found to be highly correlated with that of Ca²⁺ in the coarse mode during the YS event, whereas they were well correlated with NH₄ ⁺ during the non-YS period.     

Sulfur Deposition in Asia: Seasonal Behavior and Contributions from Various Energy Sectors

Sulfur transport and deposition in Asia, on an annual andseasonal basis, is analyzed using the ATMOS model. Calculationsare performed for two complete years (1990 and 1995). Deposition amounts in excess of 0.5 g S m^-2 yr^-1 are estimated for large regions in Asia, with values as high as 10 g S m^-2 yr^-1 in southeastern China. Annual averaged SO₂ concentrations in excess of 20 μg SO₂ m^-3 are calculated for many urban and suburban areas ofeastern China and S. Korea, with an average of 5 μg SO₂ m^-3 over most of the emitter regions. Sulfur deposition by major source categories is also studied. Southeast Asia (Indonesia, Malaysia, Philippines, Singapore)receives ～25% of its sulfur deposition from shipping activities. Sulfur deposition from bio-fuel burning is significant for most of the underdeveloped regions in Asia. Volcanoes are a major source of sulfur emissions in the PacificOcean, Papua New Guinea, Philippines and Southern Japan. Sulfur deposition is shown to vary significantly throughout the year.The monsoons are found to be the largest factor controlling sulfur transport and deposition in the Indian sub-continent andSoutheast Asia. India receives over 35% of its total depositionduring the summer months. In East Asia, sulfur deposition isestimated to be 10% higher during summer and fall than winterand spring. Model results are compared with observations from a number of monitoring networks in Asia and are found to be generally consistent with the limited observations.     

Forest canopy transformation of atmospheric deposition

Solute fluxes to the ground in open plots and under the forest canopy of different species were investigated in a number of long-term ecosystem studies in West Germany. From the canopy flux balance, rates of interception deposition and canopy/deposition interactions were assessed. Chemically, both open precipitation and throughfall are dilute solutions of H₂SO₄ and HNO₃ and their salts. For the sites investigated, mean pH in bulk precipitation ranged from 4.1 to 4.6, and in throughfall from 3.4 to 4.7. The increase in acidity after canopy passage at most sites indicates considerable interception deposition of strong acids to the forest stands, exceeding the rate of H+ buffering in the canopy. Evidence for buffering processes can be directly deduced from the fact that on sites with high soil alkalinity and high foliage base status, throughfall pH is usually higher than precipitation pH. Furthermore, the same idea can be concluded from changes in solution composition after canopy passage: the H⁺/SO _inf4 ^sup2? ratio is decreasing at most sites, while alkali earth cations from exchange processes occur in throughfall (Ca²⁺/SO _inf4 ^sup2? ratio increases). Solution composition and element flux data are presented for each of the sites, and the regional, orographical and site specific (species composition, ecosystem state) differentiations are discussed. A method for the assessment of total deposition and of canopy interactions such as H⁺-buffering and cation leaching is described, and results of calculations are shown. From these calculations it is concluded that forest ecosystems in Germany receive mean H⁺ loads of ca. 1 to 4 keq H⁺ · ha^?1 · a^?1 from atmospheric deposition. Acidity deposition rates seem to be related to a few key factors such as regional characteristics and ecosystem characteristics.     

Mapping of Base Cation Deposition in South Korea

Deposition of non-seasalt base cations (Ca²⁺ + Mg²⁺+ K⁺) in South Korea was mapped for 1994 to 1997 on a 11 × 14 km grid using the so-called inferential modeling technique. It is found that the annual mean wet deposition of non-seasalt base cations is about 290 eq ha^-1 yr^-1 with a maximum of 470 eq ha^-1 yr^-1 and a minimum of 120 eq ha^-1 yr^-1 while the annual mean dry deposition is about 130 eq ha^-1 yr^-1 with a maximum of 240 eq ha^-1 yr^-1 and a minimum 70 eq ha^-1 yr^-1. Theannual mean total deposition of non-seasalt Ca²⁺ + Mg²⁺ + K⁺ is found to be about 420 eq ha^-1 yr^-1 with the predominant range of 400 eq ha^-1 yr^-1 to 550 eq ha^-1 yr^-1 thatoccupies more than 45% of total deposition of non-seasalt base cations and dry deposition constitutes on average30% of the total base cation deposition. About 30% of the annualtotal deposition of sulfur is found counteracted by depositionof non-seasalt base cations over South Korea.     

A preliminary assessment of nitrogen-based fresh water acidification in southeastern Canada

Sulphate deposition is the primary cause of acidification in northeastern North America, and new SO₂ emission control is being implemented. However, continuation of existing levels of N deposition may undermine the environmental benefits derived from SO₂ control. This likelihood has been assessed for Canadian lakes. Maximum N deposition (～13 kg N ha^?1 yr^?1) occurs in south-central Ontario and southwestern Quebec. Regional median NO ₃ ^? levels are generally low (<5 μeq L^?1) suggesting that on average, N-based acidification is minor compared to the S-based component. However, examination of the seasonal NO ₃ ^? pattern at 5 intensively monitored basins reveals that 2 of them (in Ontario and Quebec) have incipient N saturation. A regional status for nitrogen-based acidification was qualitatively assessed by classifying survey data to identify cases of NO ₃ ^? leaching. Many lakes throughout southeastern Canada exhibit some leaching, particularly those in south-central Ontario and southwestern Quebec. While the evidence for a deposition-acidification link appears strong, sources of N other than the atmosphere should be considered for certain anomalous cases.     

Sulfur Acidity Loading in South Korean Ecosystems

The applicability of critical load (CL) methodology for thedetermination of natural terrestrial ecosystem sensitivity to sulfur acidity loading in South Korea was investigated.The sulfur critical load values, CL_maxS, were calculated for the terrestrial ecosystems of South Korea using the steady-state mass balance approach. The corresponding mapping of CL_maxS was carried out on the scale of 11 × 14 km grid cells. The estimated CL_maxS values depend on the low rate of soil chemical base cation weathering (mainly, 200–400 eq ha^-1 yr^-1), relativelylow base cation depositions (mainly less than 450 eq ha^-1 yr^-1) and base cation uptake (predominantly 300–400 eq ha^-1 yr^-1), and in significant degree on high valuesof acid neutralizing capacity. The latter in turn is connectedwith relatively high values of surface runoff (maximum 9000 m³ ha^-1 yr^-1). It has been shown that about 75%of CL_maxS values are in the range of 1000–2000 eq ha^-1 yr^-1 and about 15% are relatively low values(<1000 eq ha^-1 yr^-1). About 10% of ecosystems haveCL values more than 2000 eq ha^-1 yr^-1. The sensitiveand very sensitive ecosystems occur in the southeastern part of the country whereas the sustainable ecosystems are wide spread in the northeastern part. In accordance with sulfur critical load and sulfur deposition patterns, in 1994–1997 the CL_maxS values were found to be exceeded in about 40% of total number of Korean ecosystems, mainly in the southeastern part of the country. The average yearly valuesof exceedances varied from 176 to 3100 eq ha^-1 yr^-1.     

Spatial and Seasonal Variations in Nitrogen Leaching and Acidity across Four Acid-impacted Regions of the UK

This study examines the seasonal variability in levels of nitrogen (N) leaching and acidity in four acid impacted upland regions of the UK: the South Pennines, Snowdonia, Galloway and the Mourne Mountains. All regions are acidified, with median pH values of <5.5. The South Pennines exhibit excess sulphate concentrations an order of magnitude higher than those for other regions and have the lowest pH values of all the regions. Nitrate concentrations are highest in the South Pennines (seasonal medians 20–26 μeq l^?1) and the Mourne Mountains (seasonal medians 9–26 μeq l^?1). Surface water in the Mourne Mountains is the most highly N impacted in terms of the proportional contribution of N to acidity. All N species exhibit seasonality, with greater retention by catchment soils and vegetation in August. This seasonality is most marked in Snowdonia and least marked in the South Pennines. This implies that the South Pennines have reached an advanced stage of N saturation. Despite the reductions in S deposition, xSO₄ is the dominant anion for all sites in the South Pennine and Snowdonia regions. A strong negative relationship between the contribution of NO₃ to total acidity and DON was observed for all regions except the South Pennines. It is hypothesized that catchments dominated by organic rich soils produced more DON and have an increased capacity to immobilise NO₃. Seasonal nitrogen budgets show that over 60% of the N inputs are retained within catchments, and no site retains all incoming N throughout the year.     

模拟降水和氮沉降对准噶尔盆地南缘梭梭光合生理的影响

氮沉降和降水格局变化是目前全球气候变化背景备受关注的热点研究课题,也是荒漠生态系统的两个主要限制因子。因此,研究两者对荒漠植物的效应有助于深入了解荒漠生态系统对全球变化的响应。本文选择准噶尔盆地南缘荒漠地区的建群种梭梭(Haloxylon ammodendron)作为研究对象,设置自然降水(W0)与增加降水30%(W1)两个水分条件和自然氮沉降(N0)、增加氮素30 kg(N)·hm~(-2)·a~(-1)(N1)与增加氮素60kg(N)·hm~(-2)·a~(-1)(N2)3个施氮水平,连续处理2年,以探究降水、氮沉降及其交互作用对梭梭光合日变化及生理生态特征的影响。结果表明:降水、氮沉降及其交互作用对梭梭的净光合速率(Pn)日变化产生极显著正相关影响;同时根据梭梭Pn、胞间CO2浓度(Ci)及气孔限制值(Ls)的变化方向,推测梭梭光合"午休"主要由非气孔因素引起。此外,W0条件下,梭梭丙二醛(MDA)含量、抗氧化酶(POD、CAT、SOD)活性、可溶性蛋白(Pr)和可溶性糖(SS)含量均随施氮量增加而显著降低,脯氨酸(Pro)含量则呈先降低后增加的趋势;而W1条件下,梭梭MDA含量、抗氧化酶(POD、CAT、SOD)活性及渗透调节物质(Pro、Pr、SS)含量均随施氮量增加呈显著先增加后降低的趋势。两种水分条件下,除W1N1处理梭梭的Pro含量高于对照组外,其余处理均显著低于对照组;同时梭梭的MDA含量、抗氧化酶活性、Pr及SS含量也均显著低于对照组。综合分析结果表明:降水、增氮及其交互作用均有利于梭梭的生长,但其交互作用效应的强弱则取决于二者间的比例。     

Specifics and Temporal Changes in Air Pollution in Areas Affected by Emissions from Oil Shale Industry, Estonia

Atmospheric air pollution levels and long-term effects on the environment caused by simultaneous presence of SO₂ and oil shale alkaline fly ash during the last five decades (since 1950) were investigated. The annual critical value of SO₂ for forest (20 µg m^?3) was surpassed in 1% (～35 km²) of the study area where the load was 30–40 µg m^?3. No effect of long-term SO₂ concentrations of up to 10–11 µg m^?3 (0.5-h max up to 270 µg m^?3) and simultaneous fly ash loads of up to 95 µg m^?3 (1000 µg m^?3) on the growth and needle longevity of Pinus sylvestris was established. The yearly deposition (average load up to 20–100 kg S ha^?1) was alkaline rather than acidic due to an elevated base cation deposition in 1960–1989. Since 1990, the proportion of SO₂ in the balance of components increased: about 70–85% of the total area was affected while the ratio of annual average concentrations of SO₂ to fly ash was over 1. The limit values of fly ash for Sphagnum mosses and conifers in the presence of SO₂ are recommended.     

Atmospheric sources,transport and deposition of mercury in Michigan: Two years of event precipitation

To assess the sources, transport and deposition of atmospheric mercury (Hg) in Michigan, a multi-site network was implemented in which Hg concentrations in event precipitation and ambient samples (vapor and participate phases) were determined. Results from the analysis of 2 years of event precipitation samples for Hg are reported here. The volume-weighted average Hg concentration in precipitation was 7.9, 10.8 and 10.2 ng/L for the Pellston, South Haven and Dexter sites, respectively. Yearly wet deposition of Hg for 1992–93 and 1993–94 was 5.8 and 5.5 μg/m² at Pellston, 9.5 and 12.7 μg/m² at South Haven and 8.7 and 9.1 μg/m at Dexter. A spatial gradient in both the Hg concentration and wet deposition was observed. Northern Michigan received almost half the deposition of Hg recorded at the southern Michigan sites. The concentration of Hg in precipitation exhibited a strong seasonal behavior with low values of 1.0 to 2.0 ng/L in winter and maximum values greater than 40 ng/L in summer. The spring, summer and autumn precipitation accounted for 89 to 91% of the total yearly Hg deposition. Mixed-layer back trajectories were calculated for each precipitation event to investigate the meteorological history and transport from potential Hg source regions. Elevated Hg concentrations were observed with air mass transport from the west, southwest, south, and southeast. At each of the sites precipitation events for which the Hg concentration was in the 90th and 10th percentile were-analyzed for trace elements by ICP-MS to investigate source impacts.     

Long Term Trend of Chemical Constituents in Tokyo Metropolitan Area in Japan

In recent years, acid rain has been a social problem all over the world. In Japan, it is also a big problem especially in the metropolitan area. Then, we have measured major ions such as H⁺, Na⁺, NH₄ ⁺, K⁺, Mg²⁺, Ca²⁺, Cl^?, NO₃ ^?, and SO₄ ^2? in precipitation and dry deposition samples which had been collected at 9 sampling sites at Hiyoshi, Mita, Kashiwa, Shiki, Fujisawa, Yokosuka, Mitaka, Hachiouji, and Ashikaga in Tokyo Metropolitan area for 10 years since 1990. The average pH of precipitation in their sites was 4.56 (n=1906). As the results of multiple regression analysis showed that pH of precipitation was determined by 5 ions such as NH₄ ⁺, nssCa²⁺(non sea salt calcium), nssCl^?(non sea salt chloride), NO₃ ^?, nssSO₄ ^2?(non sea salt sulfate) in the most of the sampling sites. Therefore, it is very important to investigate the behavior of these ions to understand the acidification of rain in Tokyo Metropolitan area. In this study, a long term trend of each ion concentration in precipitation and wet deposition was also investigated the base on the data we had observed at 7 sites for 10 years by the statistical method.