Long-Term Monitoring Study on Rain, Throughfall, and Stemflow Chemistry in Evergreen Coniforous Forests in Hokkaido, Northern Japan

Long-term study on acid precipitation monitoring at suburban forests in Sapporo city showed that bulk precipitation pH were below 4.8 in recent years. Throughfall and stemflow chemistry for two main coniferous species (Abies sachalinensis and Picea jezoensis) showed different regime for pH and element deposition. The mean annual pH values of throughfall and stemflow in Picea stand were 1.0 to 1.3 units higher than that of rain collected outside the forest. In contrast, mean annual pH of throughfall and stemflow in Abies stand were 0.3 to 0.5 units higher than that of rain. Mean annual inorganic nitrogen input via throughfall and stemflow were estimated 0.41±0.11 gN/m²/yr in Abies stand, 0.44±0.13 gN/m²/yr in Picea stand. Cation input via throughfall, especially for K, in Picea stand was 1.4 times as large as that in Abies stand. Mean annual input of S in both stands was the same level. The possible effects on surface soil properties and nutrient cycling in northern evergreen conifers was discussed.     

Study on Sampling Method of Rainfall, Throughfall, and Stemflow to Monitor the Effect of Acid Deposition on Forest Ecosystem

The use of samplers for rainfall, throughfall, and stemflow was studied in Chamaecyparis obtusa forest in Kobe to develop a suitable simplified collection method for long-term monitoring of the effect of acid deposition on the forest ecosystem. A filtrating bulk sampler, widely used in Japan due to its convenience, was modified for rainfall- and throughfall-sampling. The pH value, NH₄ ⁺- and NO₃ ^?- concns. did not change within a two-week sampling period, and the collection efficiency of the modified type relative to the wet/dry sampler was 97% (mean). The three samplers (shampoo-hat, vinyl chloride tube, and gauze type) were used for stemflow sampling. Collection efficiency of the samplers was in the order of shampoo-hat> vinyl chloride tube> gauze and that of the gauze type varied significantly with rainfall condition.     

Photochemical Formation of OH Radicals in Dew Formed on the Pine Needles at Mt. Gokurakuji

Photochemical formation rates and sources of the hydroxyl (OH) radical were determined in dew water formed on the surface of Japanese red pine (Pinus densiflora) needles of declining (NO₂ polluted area) and healthy pine stands at Mt. Gokurakuji located west of Hiroshima city in western Japan. The measured OH radical photoformation rates in dew water (n=10), which were normalized to the rate at midday on May 1 at 34°N, ranged from 0.67 to 5.18 µM h^?1 (1M=1mol L^?1). The mean value (2.69 µM h^?1) was higher than that in dew water collected on a Teflon board and higher than the mean value in rain water published previously. Of the total OH radical formation rate observed in dew water on the pine needles, 16.4 % was estimated to originate from N (III) (NO₂ ^? and HNO₂) and 24.6 % was estimated to originate from NO₃ ^?. There were other sources of OH radical photochemical formation in dew water on the pine needles besides photolysis of NO₂ ^? and NO₃ ^?.     

Characteristics of Nitrogenous Air Pollutants at Urban and Suburban Forested Sites, Western Japan

Nitrogenous air pollutants including nitrogen dioxide (NO₂), nitric acid (HNO₃), nitrate (NO ₃ ^? ), ammonia (NH₃), ammonium (NH ₄ ⁺ ), and nitrous acid (HONO) were characterized at an urban forested (UF) site in Hiroshima and at a suburban forested (SF) site in Fukuoka, western Japan, using an annular denuder system for 1?year from May 2006 to May 2007 to compare the concentrations and chemical species of atmospheric nitrogenous pollutants between UF and SF sites. The proximity of the urban area was reflected in higher NO₂ concentrations at the UF site than at the SF site. NO₂ was more oxidized at the SF site because it is farther from an urban area than the UF site, which was reflected in higher concentrations of HNO₃ at the SF site than the UF site. HNO₃ and acidic sulfate is neutralized by NH₃, existing as ammonium nitrate (NH₄NO₃) and ammonium sulfate [(NH₄)₂SO₄] at the UF site. At the SF site, acidic sulfate is neutralized by NH₃, existing as (NH₄)₂SO₄, but NH₄NO₃, had scarcely formed at the SF site. A much higher HONO concentration was observed at the UF site than at the SF site, especially in winter and spring at night, which could be explained by higher NO₂ concentrations at the UF site because of its proximity to an urban area and stagnant meteorological conditions. Atmospheric HONO determination was critical in evaluating the possibility of damage to trees in UF areas.     

Vertical Distribution of Carbonyl Sulfide at Mt. Fuji, Japan

Atmospheric carbonyl sulfide (COS) mixing ratios measured over 24 h during five summer campaigns (2003–2007) in a forest at the foot of Mt. Fuji, Japan (35°21′ N, 138°43′ E; 1,300 m above sea level, a.s.l.) and at the summit (3,776 m a.s.l.) were compared. COS levels were lower at the foot than at the summit during four out of five summer campaigns. The ratios of COS mixing ratios at the foot of Mt. Fuji to those at the summit ranged from 0.7 to 0.9. These results provide evidence of biological consumption of COS in the East Asian atmospheric boundary layer. We also measured the vertical profile of ambient COS below the forest canopy. These data showed a clear gradient of COS mixing ratio: in the lowermost 1 m of the boundary layer, COS mixing ratios decreased markedly downward. Two of the different kinds of vertical distribution of COS presented here support the role of soil as a sink of atmospheric COS described by previous research using dynamic enclosure experiments.     

重庆缙云山三种典型林分穿透水和树干茎流中氮素特征研究

为研究重庆酸雨区森林生态系统中氮湿沉降在不同林分中的分布特征,以重庆缙云山为站点,于2012年5月到10月间,测定了针阔混交林、常绿阔叶林和毛竹林三种典型林分内大气降水、穿透雨和树干茎流的铵态氮(NH4+-N)、硝态氮(NO3--N)和可溶性有机氮(DON,Dissolved Organic Nitrogen)浓度,并进行系统分析。结果表明:(1)各林分降雨组分中氮浓度均值关系为:NH4+-NNO3--NDON,NH4+-N和NO3--N的最小值分别为1.84 mg L-1和1.11 mg L-1,而DON浓度不超过0.47 mg L-1;(2)相比于大气降水,各林分的穿透雨和树干流的氮浓度都有增加,林分上分布表现为:针阔混交林常绿阔林毛竹林;(3)在时间尺度上,各林分穿透雨NH4+-N和NO3--N浓度的最高值、次高值和最低值分别出现在10月份、8月份和6月份,林分间差异不显著。树干茎流无明显时间分布规律,林分间无显著差异。研究指出,降雨量不是决定氮浓度的关键因子,而林分对氮浓度的影响作用显著。     

Fog Water Chemistry at Mt. Oyama and its Dominant Factors

We have observed acid fog in Mt. Oyama since 1988. Fog events occur frequently in Mt. Oyama; 47% of the time the mountain top is covered with fog. The pH of fog is lower than that of rain collected at the fog sampling station by about 1 unit and the lowest pH was 1.95. We have also collected gas and aerosol components at the station and observed fog events by a video camera from the mountain base, where there is an air pollution monitoring station. The air quality at the fog sampling station was affected by not only the air quality at the base but also the wind direction, valley or mountain wind. It is ascertained by using back trajectory analyses that polluted air masses are transported to the base from the Kanto plains or other big urban areas, Osaka and Nagoya. When the base is polluted, the relative humidity increases, and the valley wind blows, acid fog is formed at the mountainside. In the acid fog, nitrate ion is the most abundant anion. Nitrate ion concentration correlates well with hydrogen ion concentration. The annual mean total ion concentration has not changed much since 1988, but the concentration ratio of nitrate ion to sulfate ion has increased in recent years. The nitric acid gas concentration in the station is comparable to that in urban areas, while other gas concentrations are much lower.     

Chemical Composition of Precipitation, Throughfall and Soil Solutions at Two Forested Sites in Guangzhou, South China

Rain water at two forested sites in Guangzhou (south China) show high concentrations of SO₄ ^2?, NO₃ ^? and Ca²⁺ and display a remarkable seasonal variation, with acid rain being more important during the spring and summer than during the autumn and winter. The amount of acid rain represents about 95% of total precipitation. The sources of pollutants from which acid rain developed includes both locally derived and long-middle distance transferred atmosphere pollutants. The seasonal variation in precipitation chemistry was largely related to the increasing neutralizing capacity of base cations in rainwater in winter. Soil acidification is highlighted by high H⁺ and Al³⁺ concentrations in soil solutions. The variation in elemental concentration in soil solution was related to nitrification (H⁺, NH₄ ⁺ and NO₃ ^?) and cation exchange reaction (H⁺, Al³⁺) in soil. The negative effect of soil acidification is partly dampened by substantial deposition of base cations (Ca²⁺, Mg²⁺ and K⁺) in this area.     

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.     

Fog and Precipitation Chemistry at Mt. Rokko in Kobe, April 1997-March 1998

Fog water and precipitation were collected and analyzed to study fog and precipitation chemistry. The research was carried out through one year from April 1997 to March 1998 at Mt. Rokko in Kobe. Higher fog occurrence and larger volume of fog water were observed in summer, corresponding to the trend of seasonal variation in precipitation amount. The annual mean pH value of fog water (3.80) was lower by ca. one pH unit than that of precipitation (4.74). The concentration of chemical species in fog water was ca. 7 times that in precipitation. The highest anion and cation concentrations were SO₄ ^2? and NH₄ ⁺ in fog water and Cl^? and Na⁺ in precipitation, although the Cl^?/Na⁺ equivalent ratio in both fog water and precipitation was almost the same value as that in sea water. It is considered that in the longest fog event, NH₄ ⁺ and nss-SO₄ ^2? in fog water mainly scavenged as (NH₄)₂SO₄, mainly derived from (NH₄)₂SO₄ (aerosol) in the atmosphere, NH₃ was scavenged at the growing stage, and SO₂ was also scavenged after the mature stage. NO₃ ^? in this fog event was mainly absorbed as HNO₃.     

日本御岳等地非饱和泥石流的流动机理(上)

<正> 一、前言 1983年9月长野县西部地震,使御岳发生了3600万m~3的大滑坡,其中2500万m~3的土体滑出约9km,堆积在王龙川干流河床比降4度以下的地方。据日本主要报纸和电视台报道,这次滑坡与通常的泥石流不同,其滑动土体为非饱和状态,属粉状流。 粉状流是由于孔隙气压过剩致使土体有效摩擦角减小而发生的滑动现象。过剩孔隙气压的作用方式有两种:一种是象气垫船那样,粉状体附着在气垫上;另     

Cloud Water Deposition to Forest Canopies of Cryptomeria Japonica at Mt.Rokko, Kobe, Japan

Cloud water deposition to canopies of Cryptomeria japonica at Mt.Rokko, Kobe, Japan, was estimated from throughfall measurements and fog water collections carried out during a full year. Annual cloud frequency was 11.5–15.5% and liquid water content (LWC) was 0.059 g/m³. Since cloud water deposition on to forest canopies was significantly correlated with the amount of fog water collected, the former parameter could be quantitatively derived from throughfall measurements. Annual cloud water deposition on to Cryptomeria canopies was 1420–2860 mm (Av. 2140 mm), corresponding to 90–180% (Av. 122%) of annual rainfall. The rate of deposition was higher at the mountain ridge and the forest edge than at the mountain side and the forest interior. Annual deposition of SO₄ ^2?, NO₃ ^?, H⁺ and NH₄ ⁺ from cloud water was estimated as 204, 153, 2.5 and 58 kg/ha, respectively, equivalent to 5.8–11.7 times the corresponding deposition via rain. The values are equal to, or exceed, the maximum deposition reported for Appalachian forests in the eastern United States. Multiple regression analyses indicate that cloud water deposition on to Cryptomeria canopies was significantly correlated with the following three parameters: cloud frequency, LWC, and wind speed. Thus, these three factors apparently control cloud water deposition on to forest canopies.     

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.     

Liquid and Chemical Fluxes in Precipitation, Throughfall and Stemflow: Observations from a Deciduous Forest and a Red Pine Plantation in the Midwestern U.S.A.

Wet deposition (WD), throughfall (TF) and stemflow (SF) measurements undertaken in a deciduous forest show 85% of the WD liquid flux is observed as TF and approximately 2% as SF. TF and SF were observed to be enriched in base cations and accordingly had an average pH of 6.1 and 5.9, respectively relative to a WD pH of 5.1. The seasonal variability of TF pH below the deciduous canopies was more pronounced than that of WD though both exhibited a growing season maximum, and there is evidence that the seasonal variability of TF pH below the pines is inverted relative to the deciduous canopies likely due to enhanced dust capture and buffering by calcium carbonate. TF ion concentrations differed significantly between deciduous and pine canopies during the growing season, and there is some evidence that variation in sky view factor of 0.18–0.22 is sufficient to manifest statistically differing TF composition below sugar maples. The total atmospheric flux of inorganic nitrogen to the forest is approximately 14–18 kg-N ha^?1 yr^?1 with approximately half taken up by the canopy. Associated experiments designed to quantify uncertainties in the nutrient fluxes included laboratory tests of the Aerochem automated wet-dry sampler. These experiments indicate the delay in initiating sample collection is less than half a minute for rainfall rates above 1 cm h^?1, but may increase substantially for lower precipitation rates.     

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.     

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.     

Influences of Forest Decline on Various Properties of Soils at Mt. Hirugatake, Tanzawa Mountains, Kanto District, Japan

At Mt. Hirugatake in the Tanzawa Mountains, Kanto district, Japan, the deciduous broadleaved forests have rapidly declined. In our previous studies, we reported that the amount of soil organic matter had significantly decreased at the early and final stages of forest decline, and that the soil microbial biomass also showed a large decrease at these stages, suggesting that the composition of soil organic matter might have also changed with forest decline. To clarify the influences of forest decline on the composition of soil organic matter, the amount of humic substances, optical properties of humic acid, and the amount of soil carbohydrates in surface soils at different stages of forest decline were investigated. The amounts of humic acid and fulvic acid decreased to a lesser extent at the early and middle stages of forest decline, and showed a significant decrease at the final stage. As the amount of humin significantly decreased at the early stage, it was plausible that the distinct decrease in the total carbon content of the soil surface horizons at the early stage of forest decline was induced by the decrease in the amount of humin, and at the final stage, by the decrease in the amounts of humic acid and fulvic acid. The amount of soil carbohydrates did not change appreciably with forest decline although the soil organic matter content markedly decreased. It was suggested that most of the carbohydrates in the soil surface horizons were in a stabilized form consisting of complexes with humic substances, metals, and minerals, and would not be affected by the environmental changes associated with forest decline.     

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.     

Temporal and Spatial Variations in Soil Water Chemistry at Three Acid Forest Sites

As acid deposition declines, recovery from acidification is delayed by the fact that the soil processes that earlier buffered against acidification are now being reversed. Monitoring of within catchment processes is thus desirable. However, soil sampling is destructive and not suitable for long-term monitoring at a single site, whereas sampling of soil water with suction lysimeters may be more suitable. In this paper we evaluate 8–11 years of soil water chemistry from E- and B-horizons in three acid forest soil plots within monitored catchments. Five years of sampling also included the C-horizon. To our knowledge, this is the first long-term lysimeter study including the E-horizon showing recovery from acidification, and one of few studies including the B-horizon. Soil water concentrations of SO₄ decreased significantly between –9.5 and –1.4 μeq L^-1 yr^-1, with much higher rates of change at two southern sites compared to a northern site, where levels and changes of deposition were lower. The average annual bulk deposition of S ranged between 3 kg S ha^-1 at the northernmost site to 11 kg S ha^-1 at the southernmost site. The SO₄ decline in E-horizons was smaller than the decline in deposition, which indicated leaching of SO₄ from the O-horizon. At the two southern sites, a weaker decline in SO₄ in the B-horizon compared to the E-horizon indicated desorption of SO₄. The negative trends in SO₄ were to a large extent balanced by decreases in base cations but there were also tendencies of recovery from acidification in soil solution at the southern sites by increasing pH and ANC. However, these were contradicted by increasing Al concentrations. A high influence of marine salts in the early 1990s may have delayed the recovery. Decreasing trends of the Ca/(H⁺)² ratio in the soil solution, most pronounced at one of the southern sites, suggested that the soils were becoming more acidic, although the soil solution tended to recover.