An analysis of spatial variability of the dominant ions in precipitation in the eastern United States

Data of the Multistate Atmospheric Power Production Pollution Study (MAP3S) and the National Atmospheric Deposition Program (NADP) were utilized to develop wet deposition spatial distribution patterns for the eastern United States for 1979. The ions of SO₄ ^?, NO₃ ^?, H⁺, and NH₄ ⁺ were selected for study since they are the most prominent ones found in precipitation. Total wet deposition for 1979 was normalized to one centimeter of precipitation and objectively analyzed using the Synagraphic Mapping System (SYMAP) technique. Gradients of SO₄ ^? and NO₃ ^? were found to be essentially uniform, both to the east and west of the major pollution regions. An increased gradient in normalized deposition for SO₄ ^?, NO₃ ^?, and H⁺ was found in the Appalachian Mountain region. Estimates of total wet deposition were obtained by using the normalized deposition values in conjunction with precipitation as reported by the National Climatic Center. SYMAP analyses of the estimated total wet deposition were localized in nature due to precipitation variations between sites.     

山西省太原市旱作农区大气活性氮干湿沉降年度变化特征

鉴于大气氮素沉降对整个生态系统的重要影响,我国近年来陆续开展了不同尺度的大气氮素干、湿沉降的研究,但少有农业区多年连续监测的资料。本研究利用DELTA系统、被动采样器和雨量器在山西省太原市郊区阳曲县河村旱作农业区进行了4年的监测试验,观测大气氮素干、湿沉降的时间变异。结果表明:2011年4月—2015年3月,河村4年大气活性氮NH_3、HNO_3、NO_2、颗粒态NO_3~-(pNO_3~-)、颗粒态NH_4~+(pNH_4~+)平均沉降量分别为4.50 kg(N)·hm~(-2)·a~(-1)、3.54 kg(N)·hm~(-2)·a~(-1)、2.56 kg(N)·hm~(-2)·a~(-1)、1.62 kg(N)·hm~(-2)·a~(-1)、2.75 kg(N)·hm~(-2)·a~(-1),大气氮素干沉降总量为12.38~18.95 kg(N)·hm~(-2)·a~(-1),以2011年的氮干沉降量最高,2014年的最低。2011年4月—2015年3月各月氮干沉降量与氨气沉降量之间存在显著正相关,相关系数在0.809 8~0.937 1,由此可知,该地区活性氮沉降主要受农业氨气排放的影响。河村4年雨水中NO_3~-、NH_4~+平均浓度分别为3.20 mg(N)·L~(-1)和2.43 mg(N)·L~(-1),大气氮素湿沉降11.67~41.31 kg(N)·hm~(-2)·a~(-1)。年度间氮素湿沉降存在很大差异,以2012年氮素年湿沉降量最高,2014年最低,每年大气氮素湿沉降占氮总沉降量的份额超过50%。此外,4年湿沉降中不仅NO_3~--N和NH_4~+-N之间、且二者与降雨量也呈显著线性或二次相关关系,说明降雨量对NO_3~--N和NH_4~+-N的湿沉降影响较大。本研究表明太原市旱作农区不同年份间氮素湿沉降比干沉降差异更大,且总沉降数量较高。虽然是旱作区,该地区氮素干沉降略低于湿沉降。研究结果为该地区农田氮肥施用和氮素循环监测提供了理论依据。     

Long-Term Annual and Seasonal Patterns of Acidic Deposition and Stream Water Quality in a Great Smoky Mountains High-Elevation Watershed

The recovery potential of stream acidification from years of acidic deposition is dependent on biogeochemical processes and varies among different acid-sensitive regions. Studies that investigate long-term trends and seasonal variability of stream chemistry in the context of atmospheric deposition and watershed setting provide crucial assessments on governing biogeochemical processes. In this study, water chemistries were investigated in Noland Divide watershed (NDW), a high-elevation watershed in the Great Smoky Mountains National Park (GRSM) of the southern Appalachian region. Monitoring data from 1991 to 2007 for deposition and stream water chemistries were statistically analyzed for long-term trends and seasonal patterns by using Seasonal Kendall Tau tests. Precipitation declined over this study period, where throughfall (TF) declined significantly by 5.76?cm?year^?1. Precipitation patterns play a key role in the fate and transport of acid pollutants. On a monthly volume-weighted basis, pH of TF and wet deposition, and stream water did not significantly change over time remaining around 4.3, 4.7, and 5.8, respectively. Per NDW area, TF SO₄ ^2- flux declined 356.16?eq?year^?1 and SO₄ ^2- concentrations did not change significantly over time. Stream SO₄ ^2- remained about 30???eq L^?1 exhibiting no long-term trends or seasonal patterns. SO₄ ^2- retention was generally greater during drier months. TF monthly volume-weighted NH₄ ⁺ and NO₃ ^- concentrations significantly increased by 0.80???eq L^?1?year^?1 and 1.24???eq L^?1?year^?1, respectively. TF NH₄ ⁺ fluxes increased by 95.76?eq?year^?1. Most of NH₄ ⁺ was retained in the watershed, and NO₃ ^- retention was much lower than NH₄ ⁺. Stream monthly volume-weighted NO₃ ^- concentrations and fluxes significantly declined by 0.56???eq L^?1?year^?1 and 139.56?eq?year^?1, respectively. Overall, in NDW, inorganic nitrogen was exported before 1999 and retained since then, presumably from forest regrowth after Frazer fir die-off in the 1970s from balsam wooly adelgid infestation. Stream export of NO₃ ^- was greater during winter than summer months. During the period from 1999 to 2007, stream base cations did not exhibit significant changes, apparently regulated by soil supply. Statistical models predicting stream pH, ANC, SO₄ ^2-, and NO₃ ^- concentrations were largely correlated with stream discharge and number of dry days between precipitation events and SO₄ ^2- deposition. Dependent on precipitation, governing biogeochemical processes in NDW appear to be SO₄ ^2- adsorption, nitrification, and NO₃ ^- forest uptake. This study provided essential information to aid the GRSM management for developing predictive models of the future water quality and potential impacts from climate change.     

上海地区氮素湿沉降及其对农业生态系统的影响

试验研究上海地区N素湿沉降及其对农业生态系统的影响结果表明,上海地区湿沉降中N营养盐含量较高,其中NO3-为2.587mg/L,NH4 达2.155mg/L,TIN的含量均在4.000mg/L以上。湿沉降输入到上海地区农业生态系统N营养盐的年通量较高,其中NH4 平均为26.580kg/hm2,1999年达到38.930kg/hm2;NO3-平均为31.545kg/hm2;TIN平均为58.123kg/hm2,相当于124.549kg/hm2尿素或327.980kg/hm2碳酸氢铵,1999年TIN输入量为77.750kg/hm2,相当于166.607kg/hm2尿素或438.732kg/hm2碳酸氢铵,占1998年全国化肥(N)平均施用量的35%。湿沉降中N的输入对农业生产有重要影响。     

铵硝营养对水稻氮效率和矿质养分吸收的影响

NH_4~+和NO_3~–是对植物有效的两种主要无机氮源。水稻一般被认为是偏好NH_4~+的植物,但是在NO_3~–条件下,水稻也能良好地生长。大多数关于水稻铵硝营养的报道是在pH 6.0左右的水培条件下开展的,但是对于酸性条件下水稻铵硝营养研究很少。随着土壤酸化的加重及一些边际酸性土壤被用作水稻种植,研究酸性条件下水稻的铵硝营养具有重要意义。本文采用水培试验,在pH 5.0的条件下,通过添加和不添加pH缓冲剂MES(2-(N-吗啡啉)乙磺酸),研究了NH_4~+和NO_3~–对水稻生长、氮效率和矿质养分(N、P、K、Ca、Mg、Fe、Zn、Cu、Mn)吸收的影响。结果表明,在不添加MES的条件下,水稻地上部生长(株高、叶绿素含量、干重)在NH_4~+和NO_3~–之间没有显著差异,而添加MES后,NH_4~+处理的水稻地上部生长优于NO_3~–。不管是否添加MES,NO_3~–处理的水稻地下部生长(根长、根表面积和根物质量)优于NH_4~+。水稻含氮量和氮利用效率在不同NH_4~+和NO_3~–处理之间没有显著差异,但是NH_4~+处理的水稻氮吸收效率高于NO_3~–。与NO_3~–相比,NH_4~+增加了水稻地上部P和Fe含量,而降低了水稻地上部Ca、Mg、Zn、Cu和Mn含量,对K含量影响较小。上述结果表明,NH_4~+有利于改善水稻地上部生长,提高氮吸收效率、地上部P和Fe含量,而NO_3~–则有利于水稻发根,提高地上部Ca、Mg、Zn、Cu和Mn含量。     

Simultaneous Determination of Gas and Particle Dry Deposition onto Conditioned Surrogate Surfaces

Aerodynamically designed surrogate surfaces were used to determine the relative importance of gaseous (SO₂, HNO₃, NH₃) and particulate species (SO₄ ^2?, NO₃ ^?, NH₄ ⁺, Ca²⁺) in the dry deposition flux. For 11 sampling periods, we measured the deposition fluxes, ambient gaseous concentrations, size distributions of atmospheric aerosols and some meteorological parameters in Uji. The dry deposition of the gas to a nearly perfect sink was calculated by subtracting the greased surface flux from the total deposition flux to both the greased and reagent impregnated (or water) surface. It was found that the gas phase deposition contributed significantly more (60–93%) than the particulate phase to overall deposition of sulfur and nitrogen compounds. The dry deposition velocities of the species were also calculated using the deposition fluxes and the measured ambient concentrations. Comparisons were made between the measured and modeled particulate deposition flux.     

Dry deposition measurements using water as a receptor: A chemical approach

The field measurement of dry deposition still represents a difficult task. In our approach, a 1 to 2 cm thick layer of water in a petri dish with a diameter of 22 cm, serves as a surrogate surface. The atmospheric constituents taken up by the water can be analyzed chemically by the same procedure as for the wet deposition samples. In contrast to solid surrogate surfaces, water exhibits the following advantageous properties: low and constant surface resistance, high sticking coefficient for aerosols, and predictable Sorption behavior for gases. Consequently, the deposition rates measured to the wet surface are generally higher, by up to a factor of 4 for NH₄ ⁺, Cl^?, NO₃ ^? and SO₄ ^2?, than those to a dry surface, but still smaller than the concurrent wet deposition rates. We observed the following average dry deposition rates in μmol m^?2 d^?1∶ NH₄ ⁺ 48.3, Ca²⁺ 40.7, Na⁺ 15.8, Mg²⁺ 8.4, K⁺ 4.2, H-Aci 36.4; SO₄ ^2? 57.2, Cl^? 39.2, NO₃ ^? 34.5, HSO₃ ^? 5.7, formate 4.0; acid soluble metals: Fe 2.8, Zn 0.60, Cu 0.11, Pb 0.073, Cd 0.0022. The soluble fraction of Zn, Cd, Cu, Pb and Fe in the dry deposition varied with the pH of the water phase corresponding to the adsorption tendency of these metals to oxide surfaces. The sampling method also allows tracing of regionally and locally emitted atmospheric pollutants. In our study the local pollution sources included road salting, construction work and a refuse incinerator. Finally, chemical reactions occurring in the atmosphere, such as the conversion of Cl^? to HCl by HNO₃ or the oxidation of SO₂, can be identified by evaluating the data. The method proposed is relevant to measure reproducibly the dry deposition of a variety of compounds to water bodies and moist vegetation.     

Measurements of wet and dry deposition in a Northern Hardwood forest

Inputs of wet and dry deposition were monitored at the Huntington Forest in the Adirondack Mountains of New York for two years in the open and beneath the canopy of a northern hardwood forest. In the open, ion flux estimates were similar using wet-only weekly (NADP protocol) and event collections, but bulk collections were higher for all ions except H⁺, which was much lower. These differences were due to the contribution of dry deposition and possible biotic alterations in bulk collectors. Dry deposition was estimated using air concentrations and ion-specific depositional velocities modeled with meteorological data, and contributed substantially to the input of all ions [H⁺ (45%), Na⁺ (24%), K⁺ (22%), NH₄ ⁺ (12%), Ca²⁺ (58%), Mg²⁺(43%), NO₃ ^? (55%), Cl^? (27%) and SO₄ ^?2 (26%)]. Dry input of base cations was dominated by coarse particles, whereas gaseous inputs were more important for S and NO₃ ^?. Atmospheric concentrations of SO₂ and inputs of SO₄ ^2? and H⁺ were lower at this site than sites closer to point sources of S gas emission. The importance of estimating atmospheric inputs was examined using examples of elemental budgets. For example, different estimates of the contribution of dry deposition of SO₄ ^2? (9–21 meq m^?2 y^?1) resulted in conclusions ranging from no net retention to a net loss of this element. Such differences have important implications in assessing the current and future role of atmospheric inputs in affecting elemental cycling.     

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.     

Rainfall,Stemflow, and Throughfall Chemistry at Urban- and Mountain-facing Sites at Mt. Gokurakuji,Hiroshima, Western Japan

Rainfall, stemflow, and throughfall were collected from 1996 to 1999 at two types of forest sites: (1) forests near the traffic roads and urban areas and (2) forests away from the urban areas at Mt. Gokurakuji, Hiroshima, western Japan in order to estimatethe effects of anthropogenic activities on atmospheric deposition. Rainfall deposition for major ions showed small differences between the sites. The NO₃ ^- and SO₄ ^2-concentrations in stemflow were higher at the urban-facing slope than at the mountain-facing slope. Throughfall deposition of NO₃ ^- and SO₄ ^2- was also higher at urban-facing slopes. Net throughfall (NTF) deposition (throughfall minus rainfall) of NO₃ ^- and SO₄ ^2- accounted for 77 and50% of the total throughfall deposition on urban-facing slopes, respectively, while it accounted for 44 and 23% on themountain-facing slopes, respectively. These results indicated a higher contribution from dry deposition on urban-facing slopes compared to mountain-facing slopes. Atmospheric N (NO₃ ^- +NH₄ ⁺) deposition from throughfall was estimated to be around 17–26 kg N ha^-1 yr^-1 on urban-facing slopes, which was greater than the threshold of N deposition that could cause nitrogen leaching in Europe and the United States. The highload of atmospheric N deposition may be one of the factors bringing about the decline of pine forests on urban-facing slopesof Mt. Gokurakuji.     

Estimation of Dry Deposition by Using a Filter Pack Method at Chunchon, Korea

Atmospheric gases and particulates were collected using four-stage filter-pack in Chunchon from January through December in 1999. Particulate SO₄ ^2? and NO₃ ^?, and gaseous HNO₃, SO₂ and NH₃ were analyzed. Annual average concentration of SO₄ ^2?(S), NO₃ ^?(S), HNO₃ (g), SO₂(g) and NH₃(g) were 5.75µg/m³, 4.98µg/m³, 0.33ppb, 1.52ppb and 7.25ppb, respectively. Annual dry deposition fluxes were estimated using the measured concentration and dry deposition velocity published by other research group. Annual dry deposition of S was 287kg · (km)^?2·y^?1, which accounted for about 30% of total S deposition. For N deposition, dry deposition is predominant; about 70% of total N deposition was through dry process mostly as forms of NH₃ and HNO₃.     

Atmospheric Deposition of Acidifying Components to a Japanese Cedar Forest

One-year field measurements were conducted in a Japanese cedar (Cryptomeria japonica) forest, located in Gunma Prefecture, Japan. On the basis of the meteorological and atmospheric concentration data, the dry deposition of SO₂, HNO₃, NO₂ and HCl was estimated using the inferential method. The annual dry deposition of H⁺ was estimated at 721 eq ha^?1yr^?1, which was 40% larger than the measured annual wet deposition of H⁺ (514 eq ha^?1yr^?1). Therefore, dry deposition is an important pathway for the atmospheric input of H⁺ to the forest in the study site. The contribution of each gas to the dry deposition of H⁺ was as follows: SO₂, 25%; HNO₃, 32%; NO₂, 10%; and HCl, 33%. The extremely high contribution of HCl appeared to be caused by the high emission intensity of HCl due to waste incineration in the site region. The differences between estimated deposition and throughfall and stemflow measurements indicated that about 80% of the total deposition of H⁺ was taken up by the canopy.     

Some Insights into Atmospheric Processes Involving Urban Sulphur and Nitrogen in and around Hong Kong,SAR

The representative mass ratio of the reactive airborne sulphur-to-nitrogen, S/N in the gas and aerosol phases, and in wet and dry deposition over the territory of Hong Kong, SAR,was determined, utilizing available data for the 12 yr period, 1986–1997. Using this information, the representative stoichiometric ratio values for sulphate-to-nitrate in aerosoland in wet and dry depositions were estimated. A limited supplementary data set on various canopy depositions was alsoutilized. This information collectively suggests several basicdifferences in photochemical processes between the urbanatmospheres in and around Hong Kong and the classical, smoggyLos Angeles. This is also supported by the typical diurnal variation of nitrogen oxides in Hong Kong, which suggests a moreefficient photo-oxidation of NO to NO₂ within the territoryand in nearby areas upwind, as compared to further oxidation tothe NO₃ (or nitrate) stage. On the other hand, the relatively low gas-to-particle ratio value estimated for S (～3) relative to N (～26) suggests that the advectedfraction of non-sea salt aerosol sulphate in the territory couldbe considerably greater than the corresponding fraction for nitrate. Finally, significant losses (probably related to sampling) of NH₄-NH₃ in dry deposition could be inferred, while for SO₄ in wet deposition, a moderate enrichment factor of ～2 is observed in relation to SO₄ in aerosol.     

Dry Deposition to the Forest Canopy and Surrogate Surfaces in Two Mediterranean Holm Oak Forests in Montseny (NE Spain)

The fluxes recovered from washing branches and surrogatesurfaces were compared for two holm oak (Quercus ilex L.)forests in the Montseny mountains (NE Spain) differentiallyexposed to pollution. For 5 periods in May and June 1996 afterexposures ranging between 68–189 hr, 6 metacrylate plates and 8branches were extracted with distilled water. Also, a sequentialwashing of branches was undertaken, with 5 min separationsbetween the 3 initial washes, one hour between the 3rd and the4th, and 6 hr between the 4th and the last one. The compositionwas analysed for PO₄ ^3-, SO₄ ^2-,NO₃ ^-, Cl, F, NH₄ ⁺,Ca²⁺, Mg²⁺, Na⁺, K⁺, Cu, Pb, Mn, Co, Ni and Zn. The applied techniques were consistent in that dry deposition would accountfor the throughfall fluxes of NO₃ ^-, Cl^-,Cu and Zn. Potassium and Mn would derive mostly from leaching and their fluxes were strongly related with the holm oak flower growth. ForMg²⁺ and SO₄ ^2- either leaching or impaction of small particles or gases (for SO₄ ^2-) could account forthe recovered fluxes. Also for Na⁺ and Ca²⁺ the experiments did not produce conclusive results. Ammonium, F, Pb,Co, and Na were under the detection limit of analyticaltechniques in the plate-wash. The exposed site presented higherleaf-wash and plate-wash fluxes for all elements. This wasattributed to its higher exposure to pollutants, and forleaching-derived elements, to its higher site fertility.     

水稻对硝态氮响应的生理指标筛选

采用温室水培试验方法 ,系统评价了 4 0个遗传特性不同的水稻品种对 3种比例氮营养(NH 4 /NO-3 比例分别为 10 0∶0、5 0∶5 0和 0∶10 0 )的反应和对硝态氮响应的生理指标筛选。结果表明 ,4 0个水稻品种 (系 )在NH 4 /NO-3 比为 5 0∶5 0的营养液中生长最佳 ,植株总干重最高 ,但各个基因型的表现差异较大。根据水稻在两种比例氮营养液 (10 0∶0和 5 0∶5 0 )中的表现可将水稻分为 3种类型 :硝高度响应型、硝中度响应型、硝不响应型。在混合氮营养液中硝高度响应型水稻地上部干重、根干重、总干重和氮积累量显著比单一铵营养液中的高。在评价不同水稻基因型对硝营养的响应时 ,根干物重和氮积累量可作为筛选的主要生理指标     

Nature and Magnitude of Atmospheric Fluxes of Total Inorganic Nitrogen and Other Inorganic Species to the Tampa Bay Watershed, FL, USA

We estimated the total inorganic fluxes of nitrogen (N), sulfur (S), chloride (Cl^?, sodium (Na⁺, calcium (Ca²⁺, magnesium (Mg²⁺, potassium (K⁺ and hydronium (H⁺. The resistance deposition algorithm that is programmed as part of the CALMET/CALPUFF modeling system was used to generate spatially-distributed deposition velocities, which were then combined with measurements of urban and rural concentrations of gas and particle species to obtain dry deposition rates. Wet deposition rates for each species were determined from rainfall concentrations and amounts available from the National Acid Deposition Program (NADP) monitoring network databases. The estimated total inorganic nitrogen deposition to the Tampa Bay watershed (excluding Tampa Bay) was 17 kg-N ha^?1 yr^?1 or 9,700 metric tons yr^?1, and the ratio of dry to wet deposition rates was ～2.3 for inorganic nitrogen. The largest contributors to the total N flux were ammonia (NH₃ and nitrogen oxides (NO _x at 4.6 kg-N ha^?1 yr^?1 and 5.1 kg-N ha^?1 yr^?1, respectively. Averaged wet deposition rates were 2.3 and 2.7 kg-N ha^?1 yr^?1 for NH₄ ⁺ and NO₃ ^?, respectively.     

不同沟灌方式下玉米根区矿物氮迁移动态研究

为探索交替隔沟灌溉下玉米根区矿物氮分布规律, 通过遮雨棚内微区试验, 研究了常规沟灌、交替隔沟灌和固定隔沟灌3 种沟灌方式对玉米根区硝态氮、铵态氮迁移的影响。结果表明: 交替隔沟灌溉根区硝态氮等值线和常规沟灌相似, 沟内硝态氮含量基本沿垄的中心对称分布。固定隔沟灌溉的湿润沟内硝态氮含量小于干燥沟, 施氮后非灌水沟硝态氮保持较高水平。收获时交替隔沟灌溉的根区硝态氮残留量比常规灌溉略高。与硝态氮分布相比, 铵态氮在根区土壤中的含量很小, 3 种沟灌方式在沟和垄中的铵态氮含量没有明显差异。     

Intercomparison of snow Sampling and Analysis Within the Alpine-Wide Snowpack Investigation (SNOSP)

In order to investigate the seasonal and geographical distribution of snow concentrations anddeposition fluxes of environmentally relevant ionic species in the Alps, the international programSNOSP was initiated. In the framework of this program, intercomparisons of snow samplingtechniques and analytical methods to determine the ionic species C1^-, NO ₃ ^- ,SO ₄ ^2- , K⁺, Na⁺, NH4 ⁺, Mg²⁺, and Ca²⁺, as well as the pH and the specificconductivity were performed. The concentrations of these species in the snow samples collectedin the SNOSP program varied by orders of magnitude with, e.g., concentrations of NO ₃ ^- , SO ₄ ^2- , and NH4 ⁺ ranging from 0.2-60, 0.2-90, and 0.1-60 µeq L^-1,respectively. The intercomparisons revealed a reasonable agreement of the determinations of thespecies Cl^-, NO ₃ ^- , SO ₄ ^2- , Na⁺, and NH4 ⁺ in snow. Results were less satisfactory for K⁺, Mg²⁺, Ca²⁺,and H⁺, mainly due to the very low concentrations. In conclusion, recommendations areformulated for the reliable derivation of chemical inventories from snow packs.     

Dry deposition to snow in an urban area

Ambient particle and gas concentrations, wet deposition and dry deposition were measured in Warren, MI between December 18, 1983 and April 6, 1984. Dry deposition was measured to various surfaces in a cutoff bucket, including a snow surface, a snow/water surface during melting and a deionized water surface. Dry deposition velocities were calculated for various species from the ratio of the dry flux to the ambient concentrations. The dry deposition velocities measured to a snow surface were 0.082 cm s^?1 SO₂ 2.0 for HNO₃, 0.083 for NH₄ ⁺, 2.0 for Ca⁺⁺ and 4.3 for Cl^?. The values were not significantly different for a snow/water surface during melting compared to a snow surface. However, higher values of 0.69 cm s^?1 for SO₂, 6.2 for HNO₃, 0.33 for NH₄ ⁺, and 4.2 for Ca⁺⁺ were found to a deionized water surface in the spring. These higher values could be due to the higher air temperature, the pH of the liquid or to increased atmospheric mixing during this period.     

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.