Long-Term Observation of Fogwater Composition at two Mountainous Sites in Gunma Prefecture, Japan

We made serial observations on acid fog at Mt. Akagi and Mt. Haruna, Japan for 5 years. The altitudes of the sampling sites were 1500 m (Mt. Akagi) and 1200 m (Mt. Haruna) above sea level, and the sites were approximately 30 km apart. The average liquid water content (LWC) at Mt. Akagi and Mt. Haruna was 74 mg m^?3 and 63 mg m^?3, respectively. The pH of fogwater was 2.72–7.14 (mean 3.71) at Mt. Akagi and 2.94–6.58 (mean 3.73) at Mt. Haruna. Our long-term observations indicate that there was no significant difference in the chemical components in fogwater at both sites except for ammonium ion. However, there were some cases where the chemical components of fogwater at each site were differed remarkably even in the concurrent fog event. Nitrate and sulfate ions contributed to acidification of fogwater at Mts. Akagi and Haruna and 95% of sulfate ion in the fogwater originated from air pollution. Ammonia gas in the air was the main neutralizer of acidity in fogwater. When absorption of excessive nitric acid gas over ammonia gas in the air occurred, the pH of fogwater was lowered. Our back trajectory analysis indicated that the fogwater at Mt. Akagi was mainly affected by an air mass from the Kanto Plain, including Tokyo, while the fogwater at Mt. Haruna was influenced by an air mass from large, western cities, such as Nagoya and Osaka, as well as Tokyo.     

Elevational Patterns of Acid Deposition into a Forest and Nitrogen Saturation on Mt. Oyama, Japan

Virgin fir trees have been dying on Mt. Oyama, which is located in the southwestern part of Kanto Plain, although the frequency of death seems to be reducing recently. We report elevational patterns of acid deposition in precipitation and throughfall under fir and cedar canopies and nitrogen saturation in the forest ecosystem on Mt. Oyama. The deposition fluxes of major inorganic ions in precipitation were nearly constant regardless of elevation except for hydrogen and ammonium ions, whereas the deposition fluxes of all major inorganic ions in throughfall among cedar increased. The 5-year average of annual nitrate deposition in precipitation from 1994 to 1998 showed 19.3 – 23.5 kg ha^?1 yr^?1 (annual inorganic total N deposition: 9.6 – 10.7 kgN ha^?1 yr^?1) at four sites ranging in elevation from 500 to 1252 m, whereas the deposition in both cedar and fir throughfall was over 6 times greater than that in precipitation. The average soil surface nitrate concentration in 1998 was 140 µg g^?1 (the range: 21.1 – 429 µg g^?1, n=80) and the 7-year average of nitrate concentration in stream water from 1992 to 1998 was 4.81 mg L^?1 (the range: 2.38 – 20.6 mg L^?1, n=317). Our results indicate that nitrogen saturation is occurring in the forest ecosystem because of high N deposition, probably via acid fog, on Mt. Oyama.     

Monitoring of Acid Rain over Korean Peninsula

In order to investigate the temporal and spacial deposition characteristics of acid rain, five monitoring sites were set up in the central part of Korean Peninsula. Rainwater samples were collected by wet-only sampler from 1992 to 1997. The pH and conductivity values were measured and the major water soluble ionic components were also analyzed. Ion balance between anion and cation sum was calculated to check out the data quality of samples. The acidity of rainwater was influenced by the local sources and meteorological factors such as surface wind, moving path of storm, precipitation process, and so on. Backward trajectories were depicted to investigate the effect due to moving path of weather system. The rainwater shows strong acidity in winter and weak in summer. The pH and ion concentrations were highly dependent on synoptic weather system. In addition, we sampled fog/cloud at Mt. Sobaek (BAPMoN Station) from June to August 1995 and characterized the fog/cloud chemistry according to surface wind system of sampling site. The volume-weighted mean pH of fog/cloud samples is 4.39 at Mt. Sobaek during the sampling period.     

Peroxide Concentrations in Fog Water at Mountainous Sites in Japan

Measurements of peroxide concentrations in fog water were conducted near the summit of Mt. Norikura (altitude, 2770m) in central Japan, and at the midslope of Mt. Oyama (altitude, 680m), southwest of the Kanto Plain. The concentrations of peroxide at Mt. Norikura, far from industrial regions, ranged from 3 to 120 µ M during the summer and early autumn in 1993. The potential capacity for SO₂ oxidation appears to be very high near the summit of Mt. Norikura. Analysis of the chemical composition of three-stage size-fractionated fog water samples collected at Mt. Norikura showed that the concentrations of peroxide were apparently independent of droplet size, whereas the concentrations of chemical constituents mainly derived from secondary aerosols and the acidity were higher in smaller droplets. Peroxide concentrations in fog water were low (< 5 µ M) at Mt. Oyama, located near heavy industrial areas, and lower than those in rain water sampled simultaneously (0.2–33 µ M). Especially, peroxide was scarcely detected in strongly acidic fogs (< 0.2 µ M). Peroxide might have been decomposed by SO₂ (S(IV)) oxidation in the aqueous-phase.     

A statistical model for concentration prediction at a mountain and valley station

An atmospheric statistical model for surface pollutant concentration prediction near Anderson Creek, California, has been constructed. The model can predict the surface pollutant concentration depending on meteorological variables very well. Under the assumption of constant emission rate and mixing depth, it is found from this study that the surface pollutant concentration at a mountain and valley station depends primarily on the surface wind speed, surface wind direction, geostrophic wind and surface thermal stability.     

Differences between new england coastal fog and mountain cloud water chemistry

Major inorganic ions and pH were analyzed from mountain cloud and coastal fog water event samples from New Hampshire and Maine, U.S.A. Based on marine corrected values, the medians for coastal fog were still up to three times higher in ionic concentrations and lower in pH, compared to mountain clouds. Of the acidic constituents, nitrate concentrations were considerably higher in coastal fogs, which correlates with higher concentrations of 03 measured along the New England coast. It is hypothesized that meteorological conditions permit air pollutants emitted in the northeastern US urban corridor to move relatively intact across the Gulf of Maine and to interact with the coastal fogs, which results in differences in the chemistry of coastal fogs and mountain clouds.     

Mercury accumulation in transplanted moss and lichens at high elevation sites in Quebec

Mercury deposition was monitored at two mountain sites in Quebec using transplanted lichens and moss. The terricolous lichen species Cladina rangiferina, the epiphytic lichen species Hypogymnia physodes, and the feather moss Pleurozium schreberi were transplanted from a northern Ontario boreal site to the bases and summits of Roundtop Mountain and Mt. Tremblant in southern Quebec. After 12 months, transplants of C. rangiferina sited at the base and summit of Roundtop mountain and the summit of Mt. Tremblant showed a significant increase in mercury concentration over controls (p < 0.05). The largest difference occurred at the summit of Roundtop mountain where mercury concentration was 81.4 ± 10.9 ppb as compared to 45.6 + 10.6 ppb at the control site. No significant increases in mercury concentration in P. schreberi were seen after 12 months at any site althought trends of increase were apparent. After 20 months, further significant increases in Hg content were observed in both the terricolous lichen and the feather moss at both the Roundtop Mountain base and summit sites. A significant increase in Hg content of P. schreberi was also noted at the Mt. Tremblant summit site. Over the length of the study the greatest mercury concentration increases were observed in the feather moss at the Roundtop Mountain summit site (with a 248.3 ± 30.0 ppb mercury concentration as compared to 108.3 ± 30.0 ppb in controls). No significant change in mercury concentration in the epiphyte H. physodes was found during the study. These data indicate that mercury deposition is occurring, especially to higher elevation sites. While mercury inputs at the summits may be increased by the effects of fog, increases in mercury at the base sites cannot be accounted for the same way, but may represent the importance of dry deposition processes.     

Satellite Analysis of Volcanic Clouds and Transport of Acidic Substances from Mt. Aso and Mt. Sakurajima

The satellite images of volcanic clouds in Kyushu, Japan during September–November 1989 were studied in connection with the mountain site measurement of atmospheric qualities at Unzen-Nodake and the SO₂ concentration data at Aso Volcano Museum. The images strongly indicate that many high concentration events of SO₂ were the results of the long-range transport of volcanic gas from Mt. Aso and Mt. Sakurajima to these stations. Brief comments on the 2000 eruption of Miyake-jima volcano are added.     

Hydrologic pathways and chemical composition of runoff during snowmelt in Loch Vale Watershed,Rocky Mountain National Park,Colorado, USA

Intensive sampling of a stream draining an alpine-subalpine basin revealed that depressions in pH and acid neutralizing capacity (ANC) of surface water at the beginning of the spring snowmelt in 1987 and 1988 were not accompanied by increases in strong acid anions, and that surface waters did not become acidic (ANC<0). Samples of meltwater collected at the base of the snowpack in 1987 were acidic and exhibited distinct ‘pulses’ of nitrate and sulfate. Solutions collected with lysimeters in forest soils adjacent to the stream revealed high levels of dissolved organic carbon (DOC) and total Al. Peaks in concentration of DOC, Al, and nutrient species in the stream samples indicate a flush of soil solution into the surface water at the beginning of the melt. Infiltration of meltwater into soils and spatial heterogeneity in the timing of melting across the basin prevented stream and lake waters from becoming acidic.     

Variation in ozone concentration in relation to local climate in south-west Sweden

Ozone (O₃) concentration and air temperature/relative humidity were monitored using diffusive samplers (weekly, 3 m above ground) and Tinytag loggers (10 min sampling, 1 m above ground, self-ventilating radiation shields), respectively, in the forested landscape of south-west Sweden, 40 km north-east of Gothenburg. Two forest sites were included, one at a hilltop (175 m a.s.l.), and one in a nearby (～1 km) valley (110 m a.s.l.). In addition, a valley site (～3 km from the forest sites, 60 m a.s.l.) in an agricultural landscape was included, where ozone was measured using both a UV-based monitor and diffusive sampling. At the agricultural site measurements of temperature and relative humidity were made using a radiation shield with forced ventilation and with Tinytags, as on the forest sites, in addition to observations of wind speed and the vertical temperature gradient. Furthermore, comparison with O₃ concentrations at urban and coastal sites in the region was made. The temperature dependent, systematic error of using a self-ventilating radiation shield was estimated and corrected for. It was found that the elevated forested site experienced higher O₃ concentrations and lower evening cooling rates in calm situations as compared to the forest site in the valley and in particular as compared to the agricultural site. This can be explained by a stronger coupling with the planetary boundary layer at the elevated site and more pronounced night-inversions at the valley sites. The difference in weekly O₃ concentration between the two forested sites was correlated with the difference in average minimum night-time temperature. The coastal site had the highest ozone concentrations, related largely, but not fully, to higher night-time O₃ concentrations. The urban site showed a depression in O₃ concentration associated with the combination of large NO emissions and slow air mixing during the morning traffic rush hours.     

Chemistry of Fog Water Collected in the Mt. Rokko Area (Kobe City, Japan) between April 1997 and March 2001

Fog chemistry was studied for four years (April 1997–March 2001) at Mt. Rokko (altitude 931 m) in Kobe, Japan. A collection of samples was obtained at a mountainous site close to a highly industrialized area. The samples were collected by an active string-fog collector. The summer fog was dense and frequent. The geography of Mt. Rokko is linked to the seasonality of the occurrence and the thickness of the fog. Among the meteorological parameters, the relative humidity was important for the occurrence of fog. The correlation of the concentrations of the components in fog water indicated that (NH₄)₂SO₄ and/or NH₄HSO₄ were involved in the process of the formation of fog drops in the atmosphere. The concentration of the components decreased with an increase in the liquid water content (LWC) of the fog, and the seasonal variation of the concentration of some components depended on the seasonal variation of the LWC. The equivalent ratio of NO₃ ^? to non-sea salt (nss?) SO₄ ^2? was considerably larger than that in precipitation. Ammonium ion accounted for the largest percentage of cations, which indicates that NH₄ ⁺ was an important counter cation for NO₃ ^? and nss-SO₄ ^2?. A unique fog event in which the air pollutants seemed to be scavenged stoichiometrically was sometimes observed. The methodology used for collecting fog water at 60 mL intervals provided detailed information.     

Regional Characteristics of Cooper Corrosion Components in East Asia

Copper plates were exposed under shelters at 13 sampling sites in East Asia and their corrosion was analyzed. The corrosion products were first dissolved in water and then oxalic acid. Sulfate, nitrate and chloride in the solutions were measured by ion chromatography. The amounts of the three anions significantly differed depending on the atmospheric environment at the sites. Sulfate was a major part of the anions at Chongqing and Shanghai in China. Especially, at the urban sites in Japan, nitrate remarkably changed with the seasons, and often became the large anionic component in the summer. The amounts of chloride at most sites were at higher concentration levels compared with those at the rural sites in Japan. The anions in the copper corrosion must mainly reflect the impact of acid deposition.     

Soil acidification along a topographic gradient on Roundtop Mountain,Quebec, Canada

We examined the effects that different acidic loadings have had on soil chemistry along a toposequence on Roundtop Mountain. Due to fog interception by the forest canopy, the amount of time in the clouds is a major factor determining the amount and chemistry of precipitation reaching the soil and hence, acid precipitation loading is directly related to elevation. Soils on a transect from 520 to 850 m show a pattern of chemistry that corresponds to the loading of acidic deposition. Soil solutions collected at two elevations show different levels of both SO₄ and Cl, two of the anions in fog water as well as differences in concentrations of H ion and Al. Surface horizons of soils located at 850 m have pH in water as low as 3.7; in mineral horizons base saturation is extremely low (<5%) and Al saturation exceeds 95% in many cases. In contrast, lower on the mountain slope (below 650 m), pH is slightly higher (about 4.1) and base saturation rises to over 50% for the same soil horizons. There is a clear relationship between soil acidification and position on the mountain.     

The Chemistry of Intercepted Clouds in Northern Arizona during the North American Monsoon Season

Cloudwater samples have been collected for the first time at a high-elevation site in the US interior Southwest. Cloud samples were collected at the summit of Mt. Elden near Flagstaff, Arizona. The samples were analyzed for pH, ionic composition, trace metals, organic carbon content, and volatile organic compounds. All of the samples showed high pH values (5.12–6.66), which appear to be the result of soil/crustal acid-neutralizing components. Ammonium and nitrate were the dominant ionic species. Organic carbon concentrations ranged from 3 to 18 mg/l. Volatile aromatic compounds (toluene, ethylbenzene, and xylenes) were detected, although they did not contribute significantly to the dissolved organic matter (<1% of dissolved organic carbon). Still, their aqueous-phase concentrations were substantially higher than equilibrium partitioning from the gas phase would suggest. Metal concentrations were high when compared to other cloud studies in remote areas. Overall, with the exception of pH, the cloud chemistry showed marked inter-event variability. The source of the variability was investigated using NOAA HYSPLIT dispersion calculations. Like the cloud composition, the air mass back trajectories differed widely from event to event, and consistently, air masses that passed over highly urbanized areas had higher trace metal, organic, and ion concentrations than more pristine air masses.     

Aerosol and Precipitation Chemistry during the Summer at the Summit of Mt. Fuji, Japan (3776m a.s.l.)

Aerosol and precipitation samples were obtained at the summit of Mt. Fuji, the highest peak (3776m a.s.l.) in Japan, in the summers of 1997, 1998, and 1999. The mountaintop might be affected by valley wind during the afternoon, but is located in the free troposphere during the morning. The temporal variations of chemical species in the aerosol and precipitation samples correspond with meteorological conditions. The SO₄ ^2? in the aerosol and precipitation exhibits high concentration with low temperature air mass, indicating the influence of long range transport from the Asian Continent. The contribution of the free troposphere to the chemical species obtained at the summit is estimated to be at least 30% during the summer season.     

酸沉降影响下近20年来衡山土壤酸化研究

对不同时期采自衡山东坡垂直带谱上6个典型土壤剖面Ah层和AB层的样品分析,土壤酸化指标研究结果表明,近2 0年来,由于酸沉降的影响,由花岗岩风化物发育的各类土壤,都有不同程度的酸化,表现在pH值下降,交换性酸,尤其是交换性Al3 增加,交换性盐基总量减少,盐基饱和度下降,特别是土壤酸缓冲性能和土壤酸害容量降低。相比之下,山顶的常湿淋溶土和山麓的湿润富铁土酸化更明显,而山体中部的常湿富铁土酸化进程较慢,山体上部的常湿雏形土酸化进程更慢,表明土壤酸化除了与土壤酸沉降量有关外,还与土壤类型有关     

巴尔鲁克山山地灰褐色森林土壤的研究

本文根据调查研究的结果,说明了巴尔鲁克山山地森林土壤与天山北坡的山地森林土壤,从生物气候带所形成的森林植被类型、成土条件、成土过程和森林土壤的基本属性都极为相似,因此应划定同属于天山北坡的灰褐色森林土。前人将它划定为同属于阿尔泰山西南坡的山地灰色森林土是不适宜的。     

Urban BTEX Spatiotemporal Exposure Assessment by Chemometric Expertise

Normative regulations on benzene in fuels and urban management strategies are expected to improve air quality. The present study deals with the application of self-organizing maps (SOMs) in order to explore the spatiotemporal variations of benzene, toluene, ethylbenzene, and xylene levels in an urban atmosphere. Temperature, wind speed, and concentration values of these four volatile organic compounds were measured after passive sampling at 21 different sampling sites located in the city of Trieste (Italy) in the framework of a multi-year long-term monitoring program. SOM helps in defining pollution patterns and changes in the urban context, showing clear improvements for what concerns benzene, toluene, ethylbenzene, and xylene concentrations in air for the 2001–2008 timeframe.     

贵阳市及其郊区土壤大气界面间汞交换通量的初步研究

利用动力学通量箱与高时间分辨率测汞仪联用技术对贵阳市市区及其郊区4个点的土壤大气界面间的汞交换通量进行了测定,用小型多功能气象仪记录了采样期间的气象参数。结果显示:4个采样点的大气汞含量都明显高于全球背景值(1.5~2.0 ng m-3),显示出贵阳市市区及郊区都遭受了不同程度的大气汞污染。土壤大气界面间的汞交换通量与光照强度具有显著的相关关系,与土壤温度也有很好的相关性。     

Acid deposition at the summit of Mt. Fuji: Observations of gases,aerosols and precipitation in summer,1993 and 1994

Intensive observations of chemical species in aerosols, gases and other samples at the summit of Mt. Fuji and at Tarobo (at 1300m on the mountain'ts southern slope) was performed from July 28 to Aug. 3, 1993 and from July 25 to 30,1994. The most interesting observation was the abrupt increase in the sulfate concentration in aerosol collected in July, 1993 just after the typhoon (number 9306) passed the Japanese archipelago and the wind direction shifted from south to west. Chemical analysis indicated this aerosol was acidic. In contrast, the summit aerosol observed in 1994 was not acidic following a less dramatic rise in sulfate content. Back trajectory analyses were used to extrapolate from these measurement to an inventory of polluted air over the Asian Continent. The concentrations of gaseous SO₂ and HCl remained low during both observation periods, with some higher concentrations of NH₃.