Geographical and Temporal Variations of Chemical Constituents in Winter Precipitation Collected in the Areas along the Coast of the Sea of Japan

The geographical and temporal variations of chemical constituents in winter precipitation collected in the areas along the coast of the Sea of Japan (AASJ) were discussed by analyzing the data obtained in the 1st and 2nd National Acid Deposition Survey by Japan Environmental Laboratories Association. In western Tohoku (WT) and Hokuriku (HR) areas in AASJ, in spite of large amounts of precipitation in winter, concentrations of non sea salt (nss-)SO₄ ^2? are not as low as the other areas, and nss-Ca²⁺ in these areas is lower than the other areas. As a result, H⁺ concentrations of precipitation in these areas are somewhat higher than other areas. From the temporal analysis of daily sampled data and back trajectory analysis of air mass, it was found that the concentrations of nss-SO₄ ^2?, NO₃ ^?, NH₄ ⁺ and nss-Ca²⁺ are correlatively varied when air mass come from the Asian Continent, showing higher concentrations at the western sites in AASJ and depending on the meteorological conditions such as the direction of in flow air mass.     

Long-Term Trends in the Chemical Composition of Precipitation over Western Japan

Wet deposition monitoring was conducted at six rural stations in western Japan, during the period from 1987 through 1996. Long-term trends in the concentration of non-sea salt ions were analyzed on the basis of the data obtained. The monitoring results indicated that annual average concentrations of NO₃ ^? and NH₄ ⁺ in precipitation significantly increased on the order of 45%, and that of nss-Ca²⁺ and nss-SO₄ ^2?, concentrations did not change over the past 10 years. The ratio of NO₃ ^?/nss-SO₄ ^2? in precipitation significantly increased, the ratio of NO₃ ^?/NH₄ ⁺ showed no marked fluctuations, and the ratio of [nss-Ca²⁺+NH₄ ⁺]/[nss-SO₄ ^2?+NO₃ ^?] slightly increased during the period. These findings suggested that the wet deposition of NO₃ ^? and NH₄ ⁺ in western Japan, particularly that in the winter season, was influenced by the long-range transport of nitrogen oxides and ammonia from the Asian continent.     

Characteristics in Concentration of Chemical Species in Ambient Air Based on Three-Year Monitoring by Filter Pack Method

Continuous monitoring of concentrations of particulate matter and gaseous compounds for three years by a four-stage filter-pack method clarified the characteristics in the concentrations of chemical species in particulate matter and gaseous compounds in ambient air in Kobe, Japan. The amount of materials in blank filters was low enough for this method to be used for the monitoring of ambient air. Little or none of the hydrogen chloride was derived anthropogenically. The concentrations of both particulate sulfate and sulfur dioxide in spring and summer were significantly higher than those in autumn and winter. The concentration of gaseous nitric acid was high in summer, which suggests that active photochemical reactions in the atmosphere provided more nitrogen species in summer. The measured concentration products [HNO₃][NH₃] showed good agreement with the theoretical predictions with some exceptions. The total concentration of ammonium species showed no significant seasonal variation except that the concentration in winter was low. The concentration of nss-Ca²⁺ in spring was significantly higher than that in the other seasons, which is most likely associated with the so-called yellow-sand events. The concentrations of nss-K⁺ and nss-Ca²⁺ accounted for most of K⁺ and Ca²⁺, respectively, whereas that of nss-Mg²⁺ accounted for only 5% of Mg²⁺     

Sulphur and nitrogen deposition in Norway,status and trends

The total deposition of sulphur (S) and nitrogen (N) components in Norway during the period 1988–1992 has been estimated on the basis of measurement data of air- and precipitation chemistry from the national monitoring network. There are large regional variations in depositions with highest values in the southwestern part of Norway. Time series analysis of annual mean concentrations of sulphur dioxide (SO₂) and sulphate (SO₄ ^––) in air, non marine SO₄ ^––, nitrate (NO₃ ^–) and ammonium (NH₄ ⁺) in precipitation, shows a significant reduction in the S concentrations both in air and precipitation. In precipitation the concentrations are reduced by 30–45 percent in Southern Norway and 45–55 percent in Central and Northern Norway. Even larger reductions are observed in air concentrations with 50–65 percent reduction in Southern Norway and 65–88 percent reduction further north. For N components there are generally no significant trends in concentration levels nor in precipitation or air. The observed trends are comparable with reported trends in emission.     

Mercury deposition and sources for the upper great lakes region

Mercury concentrations and depositions for northeastern Minnesota were measured in precipitation to investigate depositional trends, relationships with major cations and anions, and possible source emission regions. Results for 1987–1990 showed that environmentally significant amounts of Hg are present in precipitation and air and are subsequently deposited to remote lake watersheds. Volume-weighted concentrations of total Hg in precipitation averaged about 18 ng Hg L⁻¹ with calculated annual depositions near 15 μg Hg m⁻². Mercury concentrations in precipitation are positively correlated with the major ions, conductivity, and pH, and are negatively correlated with precipitation volume. The best predictor equation from stepwise regression has an r² of 0.65 with Mg and chloride concentrations as predictor variables. From measurements of Hg in rain concentrations as a function of time within events, scavenging ratios for “washable” Hg were calculated to be 140 ± 80 (mass based at a 1 mm hr ⁻¹ precipitation rate). Up to about 10% of the total Hg in air is subject to washout by precipitation for a given event. Air parcel back-trajectories indicate that possible source regions within 72-hr travel time were located mostly to the south, southeast, and southwest, up to 2500 km distance away but local sources may also be important.     

Comparison of the Chemical Composition of Precipitation on the Western and Eastern Coasts of Korea

Precipitation samples were collected at two coastal sites on the Korean Peninsula, Kangwha on the western coast and Yangyang on the eastern coast, from September 1991 to February 1997. The samples were analyzed for concentrations of major ions, in addition to pH and electrical conductivity. The annual volume-weighted mean pH values were 4.89 and 5.05 at Kangwha and Yangyang, respectively. The pH was generally lower at Kangwha than that at Yangyang, especially during the winter, because of reduced neutralizing inputs and greater acid inputs in winter. Dominant ions were different with NH₄ ⁺ and SO₄ ^2- most important at Kangwha and Na⁺ and Cl^- at Yangyang. Neglecting sea salt components, nss-SO₄ ^2- and NO₃ ^- were important anions and nss-Ca²⁺ and NH₄ ⁺ were important cations at both sites. Concentrations of these ions were 1.2–1.6 times higher at Kangwha than at Yangyang. Annual mean concentrations of these ions varied little during the study, while larger seasonal variations were observed. Annual mean nss-SO₄ ^2-/NO₃ ^- ratios at Kangwha and Yangyang were 2.8 and 2.6. The 5 yr annual mean values of nss-SO₄ ^2-/NO₃ ^- showed no trend at Kangwha but a decreasing tendency at Yangyang. The decreasing trend is similar to the decreasing trend in emissions of SO₂/NO_x in South Korea. Regional differences in chemical composition between Kangwha and Yangyang appear to be associated with long-range transport of acidic gases and alkaline dust originated from other regions.     

Geochemical Characteristics of Acidic Stream Water on Yakushima Island,a World Natural Heritage Site

We determined the chemical compositions of acidic stream waters on the rural, mountainous island of Yakushima (YK), and compared them with those of near-neutral stream waters in other mountainous watersheds in Japan. The pH and concentrations of the predominant sea-salt components (i.e., Cl^?, Na⁺, Mg²⁺) in YK water, particularly in streams with small watersheds, decrease with elevation, while the concentration of Al increases. In contrast, water in northwestern YK contains higher concentrations of non-sea-salt SO₄^2? and NO₃^? and of rock-derived cations such as Si and Ca²⁺ than water in eastern to southern YK. This clearly shows that the anthropogenic pollutants on YK are dominantly derived from the northwestern to western Asian continent rather than from Japan's main islands, which lie to the northeast. These pollutants are responsible for stream acidification on YK and for accelerating chemical weathering, mainly of plagioclase, in northwestern YK. Large amounts of acid rain on YK may enhance the formation of secondary minerals that strongly adsorb heavy metals, which can partly account for the low concentrations of heavy metals in YK waters.     

Leaching of nutrients and major ions from an arable field with an unfertilized fallow as infield buffer zone

Abstract

Leaching of nutrients and major ions from a tile-drained arable field was evaluated over a 25-year period (1980–2005). The soil, classified as a Gleyic Cambisol, received moderate applications of fertilizers. During later years the soil was more frequently under ley, and since 2002, an area of ravine (29% of the total field) has been managed as a permanent fallow with annual cutting without removing the grass material. A decrease in the concentration of nitrate nitrogen (NO₃?N) in the drainwater was estimated in 1980–2005, based on non-parametric tests on concentrations flow-normalized with a robust fitting curve procedure. The average concentration of soluble reactive phosphorus after pre-filtration (RP_f) of 0.030 mg l^?l corresponded to a calculated degree of phosphorus saturation (DPS) of 6% in acid extract of ammonium lactate from the topsoil. Between 1995 and 2005, concentrations of suspended solids (SS), RP and total organic carbon (TOC) decreased significantly in the drainage water from the entire field. Throughout the entire period, there was a negative net accumulation of the major ions to the soil. The order of decrease in relative terms was calcium (Ca²⁺)>magnesium (Mg²⁺)>sulphate (SO₄ ^2?)>chloride (Cl^?)>potassium (K⁺). In addition, the soil phosphorus (P) balance was negative. A significant reduction in ion concentrations in the drainwater, including sodium (Na⁺) and hydrogen carbonate HCO₃ ^?, was estimated. The order of reduction in relative terms was: SO₄ ^2?>Mg²⁺>Ca²⁺>HCO₃ ^?>Cl^?>NO₃ ^?>Na⁺>HPO₄. Altogether these trends were equal to approximately 0.1 mmol_c l^?1. yr^?1 of positively and negatively charged ions. Based on measured concentrations, decreasing trends in SO₄ ^2? and Ca²⁺ were also observed in the shallow groundwater (3.6 m below the soil surface), while K⁺, Na⁺ and HCO₃ ^? tended to increase. Trends of cations in deeper groundwater (5.8 m below the soil surface) were in some cases the opposite of the trends in the drainwater.     

Regional Differences in the Relation Between Monthly Precipitation and Bulk Concentration in France (Renecofor)

Bulk precipitation was sampled weekly from 1993 to 1994 at 27 sites, covering the whole country. In this paper the relations between decreasing concentrations of 4-weekly mean weighted samples with increasing 4-weekly precipitation are studied using two types of equations: (i) y = a+b/x; (ii) y+1= ax^b, where y = concentration of an ion and x = 4-weekly precipitation quantity. Relationships were studied for the major ions. H⁺ did not show any relationship with the rainfall amount. From the 216 regressions (27 sites × 8 ions) for all the other ions, 55.6% showed a good fit (r equal or above 0.6) and 16.2% a very good fit (r equal or above 0.85). Good fits were found for 85% of the regressions for N-NO₃ ^-, 81% for S-SO₄ ^2-, 63% for Ca²⁺, 59% for K⁺, 55% for N-NH₄ ⁺, 37% for Mg²⁺, 33% for Cl^- and 29% for Na⁺. The comparison between sites for the same ions showed: (i) the ranking of the sites after the regressions from lower to higher concentration levels does not necessarily correspond to the ranking of the sites bi-annual mean weighted concentrations; (ii) sites showed similar behaviour for certain ions for which an explanation could be found, based on local or regional emission characteristics or air mass influences, and for others this was not possible; (iii) for certain ions and pairs of sites, comparable annual precipitation led to comparable behaviour, for others precipitation was not an explanatory factor at all, (iv) local and regional influences seem to have a much greater impact on decreasing concentrations than the gradient from the Atlantic coast to the eastern French border.     

Characterizinig Precipitation Chemistry in Changhua, Central Taiwan Using Weather Conditions And Multivariate Analysis

Few studies of atmospheric deposition come from the fast growing region of Southeast Asia. Precipitation in Changhua City in central Taiwan was collected to examine its chemical composition and relationship with meteorological patterns. Fifty percent of the precipitation measurements had pH<5.0. Deposition fluxes of most ions were comparable to that reported for heavily industrialized temperate regions. Storms associated with air masses which originated in China had higher ion concentrations than other storms, suggesting substantial contribution of long-range transport. Two factors, a sea salt factor and an anthropogenic factor, explained more than 70% of the variation in precipitation chemistry. A third factor had a high loading only on H⁺, suggesting that pH of precipitation in Changhua City was not dominated only by acidic or basic ions alone. Instead it is determined by all components. The influences of soil and dust, as indicated by high loading on Ca²⁺ and K⁺, cannot be recognized without sea salt correction.     

Precipitation and streamwater chemistry from undisturbed watersheds in the cascade mountains of Oregon

Long-term records of precipitation and streamwater chemistry are rare; such records from forested watersheds relatively free of acidic deposition are even rarer. Precipitation and streamwater chemistry have been measured on two undisturbed forested watersheds at the H. J. Andrews Experimental Forest located on the western slopes of the Cascade Mountains of Oregon. Data from one watershed spans the period 1973–1985, the other 1969–1985. The mean annual pH of precipitation was 5.5 with a range of 4.7 to 6.0. HCO₃ ^? was the dominant anion; Ca²⁺ and Na⁺ were the dominant cations. The mean annual pH of streamwater was 7.3, and was dominated by HCO₃ ^? and Ca²⁺. These data contrast sharply with data from other calibrated watersheds in the north Cascade Mountains of Washington and British Columbia, and with data from New Hampshire and North Carolina where pH of precipitation averages 4.14 and 4.43, respectively, with SO₄ ^2? the dominant anion.     

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.     

Source Identification of Rural Precipitation Chemistry in Japan

Precipitation chemistry was discussed from the viewpoint of potential sources for four rural sites where wet-only daily-basis measurement data sets were available during the period from April 1996 to March 1997 in Japan. Annual volume-weighted mean concentrations of nss-SO₄ ^2? and NO₃ ^? ranged from 18.0 to 34.6 µeq L^?1, and from 9.3 to 23.1 µeq L^?1, respectively. The degree of neutralization of input acidity in terms of the concentration ratio, [H⁺] / ([nss-SO₄ ^2?] + [NO₃ ^?]), ranged from 0.46 to 0.63. This suggests that about half of the input acidity due to H₂SO₄ and HNO₃ was neutralized by NH₄ ⁺ and nss-Ca²⁺ to produce the pH values of 4.46 to 4.82 for these sites. Maximum likelihood factor analysis was then performed on the logarithmically transformed daily wet deposition of major ions. Two factors successfully explained a total of about 80% of the variance in the data for each site. Interpreting varimax rotated factor loadings, we could identify two source types: (1) acid source with large loadings on ln(H⁺), ln(nss-SO₄ ^2?), ln(NO₃ ^?) and ln(NH₄ ⁺), (2) sea-salt source with large loadings on ln(Na⁺), ln(Cl^?), ln(Mg²⁺) and ln(K⁺). The rural wet deposition over Japan appears to have a similar structure in terms of the kinds of sources and their relative location.     

Chemical Characteristics of Fog Water at Mt. Tateyama, Near the Coast of the Japan Sea in Central Japan

Measurements of the chemical composition of fog water at Murododaira (altitude, 2,450 m), on the western slope of Mt. Tateyama near the coast of the Japan Sea, were performed each autumn from 2004 through 2007. Strong acidic fogs (pH?<?4) containing high concentrations of nssSO ₄ ^2? were frequently observed in the autumn of 2005, when the air mass at Mt. Tateyama originated mainly from the polluted regions of Asia. The ratio of NO ₃ ^? /nssSO ₄ ^2? in fog water was relatively high in 2004 and 2007. High concentrations of nssCa²⁺ derived from dust particles were detected in 2006. Background Kosa particles might have been predominant in the free troposphere and could have neutralized acidic fogs in the autumn of 2006. High concentrations of sea-salt components were also observed in October 2005. The sea-salt particles might have been transported from the Pacific Ocean by a strong typhoon, and significant Mg²⁺ loss was observed. Peroxides higher than 100 μM, which are seriously harmful to vegetation were sometimes detected.     

Acidic precipitation at a site within the northeastern conurbation

Rain and snow were collected in plastic beakers either manually or with a Wong sampler during 58 precipitation events in 1974 at Yonkers, New York approximately 24 km north of the center of New York City. Determinations were made of total dissolved ionic species, free H ions, total H ions, sulfate, nitrate, chloride, and fluoride. Conductivity measurements ranged from 6.8 to 162 gmhos, pH from 3.4 to 4.9, total acidity from 36 to 557 μeq 1^?1 sulfate from less than 1 to 20 mg 1^?1, nitrate from less than 1 to 14 mg 1^?1, and chloride from less than 1 to 7 mg 1^?1. All fluoride concentrations were less than 0.1 mg 1^?1. The results indicate that precipitation at this suburban location adjacent to New York City is consistently acidic and contains concentrations of sulfate, nitrate, and chloride which are similar to values found for other locations in the northeastern United States. Positive correlations were found between nitrate and sulfate concentrations and acidity suggesting that the atmospheric contaminants, SO₂, and NO₂ are causally-related to the occurrence of acidic precipitation. Further research will be necessary to clarify the relative influence of natural and man-made sources of N and S compounds and the contributions of gaseous and particulate contaminants in the atmosphere to the acidity of precipitation at this location.     

新疆伊犁察南灌区土壤盐分特征

以察南灌区土壤为研究对象,对不同含盐量土壤进行盐化程度分级,并对该地区土壤盐分特征进行相关分析和主成分分析,以及对土壤盐分因子区域影响因素进行探讨。结果表明:察南灌区以碱性土壤为主,HCO_3~–是影响该灌区土壤p H最强的因子;对灌区0~100 cm土体土壤的分析表明,灌区盐化土面积约为总灌溉面积的1/4,盐渍化风险较大;相关性分析显示,HCO–3、Cl~–、SO_4~(2-)、Ca~(2~+)、Mg~(2~+)、Na~+、K~+为盐分主要组成离子,总盐分与各离子之间均呈正相关关系,与总盐分相关性最强的阴离子为SO_4~(2-),相关性最强的阳离子为Mg~(2~+);主成分分析显示,HCO_3~–、Cl~–、K~+为影响该灌区土壤盐分特征的主导因子;通过盐分因子区域影响因素定性分析可知,除HCO_3~–和pH是由河流以及地下水综合作用影响外,其他盐分因子均主要受河流影响。     

Snowcover Components in Northern Japan

Snowcover surveys were carried out in Hokkaido, northern Japan. Snowpack samples were collected using a steel pipe at 80 sites in 1988, 69 sites in 1992, and 66 sites in 1996 and 2000 during the time when the water equivalents of the snowcover are the greatest. Spatial distribution maps of water equivalents and of the concentrations and the accumulated amounts of hydrogen, non-sea-salt sulfate and non-sea-salt calcium ion of the snowcover drawn by Kriging method are discussed. The distribution maps show that water equivalents and the accumulated amounts of hydrogen and non-sea-salt sulfate in all the sample years were largest in the Japan Sea region, as were the ion concentrations of hydrogen and non-sea-salt sulfate. It was estimated this was caused by air pollutants transported from a great distance. The ratio of areas below pH 5.0 increased temporally from 1988 (20%) to 1992, 1996 and 2000 (66–80%). This trend was estimated to be affected by a decline of non-sea-salt calcium concentrations derived from alkaline road dust. In addition, the effect of snowcover components was assessed by comparison between the acid loads of the snowcover and the acid neutralizing capacity of lake water. We found that lakes in the middle of the Japan Sea coast have the potential to be acidified by snowmelt.     

Seasonal and Annual Fluxes of Inorganic Constituents in a Small Catchment of a Japanese Cedar Forest near the Sea of Japan

Fluxes of major ions in rainfall (RF), throughfall plus stemflow (TF + SF), and stream water (SW) were measured for five water years in a small catchment of a Japanese cedar forest near the Sea of Japan. The fluxes of most ions in RF and in TF + SF, including the non-sea-salt constituents, increased from late autumn to midwinter owing to the seasonal westerly wind. The concentrations of most ions in SW showed no obvious seasonal trend during the study period, whereas ${\text{NO}}_3 ^ - $ concentrations were lowest in summer, with a small seasonality. The Ca²⁺ and Mg²⁺ outputs in SW were approximately 3.7 and 1.8 times the TF + SF inputs of these cations, respectively. The large net outputs of base cations in the catchment may indicate a decrease in the soil's acid-neutralizing capacity. Annual dissolved inorganic nitrogen inputs in RF and in TF + SF were 17.7 and 17.9 kg N ha^?1 year^?1, respectively, which exceeded previously published thresholds in Europe and the U.S. (i.e., the values at which these inputs increased ${\text{NO}}_3 ^ - $ levels in SW) and equaled the highest level of nitrogen deposition previously reported in Japan. The ${\text{NO}}_{\text{3}} ^{\text{ - }} $ concentrations in SW were relatively high even in summer. During high-precipitation events, ${\text{NO}}_{\text{3}} ^{\text{ - }} $ concentrations in SW increased with increasing water discharge, and the pH decreased simultaneously during several events. Nitrogen deposition may contribute to the high ${\text{NO}}_{\text{3}} ^{\text{ - }} $ concentrations in SW and the temporary acidification that occurred during the rain events.     

Precipitation chemistry in Japan 1989–1993

Precipitation chemistry in Japan was discussed on a wet-only sample database obtained in a nationwide survey from April 1989 to March 1993. Wet-only samples were collected at 29 stations over Japan on a biweekly basis. Commonly determined chemical parameters were measured in laboratories. The volume-weighted annual mean pH at each site ranged from 4.50 to 5.83 with a mean of 4.76. Concentration ranges and means (parenthesized) on an equivalent basis for major ions were as follows: nss-SO₄ ^2–; 5.2–58.9 (38.6), NO₃ ^–; 1.8–25.0 (14.1), NH₄ ⁺; 0.55–29.8 (18.3), nss-Ca²⁺; 2.0–34.5(14.2), Na⁺; 6.4–275.3 (49.1), Cl^–; 13.7–322.4 (63.5) eq L^–1. Acid-base relationships for Phase-II records were quantitatively discussed in terms of three measures: pH, fractional acidity, and our proposed pA_i.     

Wet deposition trends of major inorganic ions in Finland based on daily bulk deposition samples

Trends in the precipitation-weighted average concentrations and in the deposition of inorganic ions in daily precipitation samples at three Finnish background stations were calculated for a period extending from the seventies to 1988. During the period 1973–1988, S0₄ ^2? concentrations in wet deposition at the station in Central Finland decreased by 39% in accordance with the emission decrease of SO₁ in Finland of 50% over the same period, and the 20% decrease in Europe from 1980 to 1988. However, due to the more significant decrease in alkaline ions (80% for Mg²⁺), H⁺ concentrations increased by 30%. At the two southernmost stations, overall concentrations are higher and the decrease of Mg²⁺ and Ca²⁺ is less important, but at the station in southeastern Finland the increase of N0₃ ^? relative to NH₄ ⁺ has doubled H⁺ concentrations during the period 1977–1988. Division of the data according to wind direction sectors showed generally decreasing concentrations in the sectors related to Scandinavia, but unchanging or increasing concentrations in the sectors related to eastern Europe. Acid deposition trends were estimated as H⁺, S0₄ ^2? - (Ca²⁺ + Mg²⁺), and H⁺ + NH₄ ⁺ - N0₃ ⁺. All these trends showed increasing acid deposition in central Finland and decreasing trends in western Finland. In eastern Finland the trends were opposing due to the increasing N0^{3 +} but decreasing NH₄ ^? trends. It is concluded that S0₄ ^2? deposition trends do not reflect acid deposition trends, and SO₄ ^2? or N0₃ ^? deposition do not geographically represent acid deposition.