Method to estimate atmospheric deposition of base cations in coniferous throughfall

A convenient non-electric method for estimating the dry deposition of base cations on a coniferous forest is presented. The dry deposition is estimated by multiplying the ratio of the base cation deposition to the sodium deposition on a surrogate surface with the dry deposition of sodium on the forest stand (throughfall technique). The surrogate surface is designed to resemble the needles in a coniferous forest with respect to particle deposition. Atmospheric non-marine dry deposition measured using the surrogate surface was compared to model calculated depositions. There was a good agreement for calcium but not for potassium.     

Atmospheric deposition in forest edges measured by monitoring canopy throughfall

Atmospheric dry deposition in two forest edges was studied by means of monitoring canopy throughfall in Douglas Fir stands. Throughfall fluxes in the first 50 to 100 m of forest edges were found to be substantially higher than fluxes in the interior of forest stands. Sodium and chloride showed the steepest throughfall flux gradients. Ions important for soil acidification and eutrophication showed relatively less steep but still significant gradients. The mean increase of the throughfall flux at 10 m, with respect to the flux at 200 m from the forest edge amounted to 150% for Na⁺, 119% for Cl^?, 54% for S0₄ ^2?, 38% for NO₃ ^? , and 39% for NH₄ ⁺ The enhancement of dry deposition in forest edges strongly depends on wind velocity and wind direction during dry deposition. Particularly trees in forest edges exposed to prevailing wind directions receive relatively large amounts of dry deposition.     

Above-Ground Sulfur Cycling in Adjacent Coniferous and Deciduous Forests and Watershed Sulfur Retention in the Georgia Piedmont,U.S.A.

Atmospheric deposition and above-ground cycling of sulfur (S) were evaluated in adjacent deciduous and coniferous forests at the Panola Mountain Research Watershed (PMRW), Georgia, U.S.A. Total atmospheric S deposition (wet plus dry) was 12.9 and 12.7 kg ha-¹ yr-¹ for the deciduous and coniferous forests, respectively, from October 1987 through November 1989. Dry deposition contributes more than 40% to the total atmospheric S deposition, and SO₂ is the major source (～55%) of total dry S deposition. Dry deposition to these canopies is similar to regional estimates suggesting that 60-km proximity to emission sources does not noticeably impact dry deposition at PMRW. Below-canopy S fluxes (throughfall plus stemflow) in each forest are 37% higher annually in the deciduous forest than in the coniferous forest. An excess in below-canopy S flux in the deciduous forest is attributed to leaching and higher dry deposition than in the coniferous forest. Total S deposition to the forest floor by throughfall, stemflow and litterfall was 2.4 and 2.8 times higher in the deciduous and coniferous forests, respectively, than annual S growth requirement for foliage and wood. Although S deposition exceeds growth requirement, more than 95% of the total atmospheric S deposition was retained by the watershed in 1988 and 1989. The S retention at PMRW is primarily due to SO₄ ²- adsorption by iron oxides and hydroxides in watershed soils. The S content in white oak and loblolly pine boles have increased more than 200% in the last 20 yr, possibly reflecting increases in emissions.     

Trends in Sulphur and Nitrogen Deposition Fluxes in the GEOMON Network, Czech Republic, between 1994 and 2000

Deposition fluxes of sulphur and nitrogen in bulk and throughfall precipitation were monitored for the 1994–2000 period for seven small forest catchments in the GEOMON network, Czech Republic (CR). Four catchments are situated at similar elevations (roughly between 800 and 1000 m) and represent three areas: the Black Triangle near the Kru?né hory Mts. coalfield (catchments JEZ and LYS), the Orlické hory Mts., close to the Polish industrial regions (UDL), and the ?umava Mts., a relatively unpolluted area (LIZ). Three catments (GEM, POM, LES) lie at lower elevations (400–600 m) in Central Bohemia. A substantial decrease in the bulk and throughfall deposition of pollutants occurred as a result of the desulphurisation programme implemented in the Czech Republic between 1996 and 1998. A reduction has been described mainly in the Kru?né hory Mts. (JEZ), in Slavkovský les (LYS) and also in Central Bohemia (GEM). The decrease in the throughfall to less than one half within a single year in POM (Central Bohemia) was an example of a direct response to the local emission reduction in the nearby Chvaletice power plant. However, in some areas, the throughfall deposition of sulphur, which includes wet and dry deposition, is still significant, especially at higher elevations. Recent forest degradation was observed in the Orlické hory Mts., where, particularly in 1998, as much as 91.1 kg S was found in coniferous throughfall. The fraction of dry deposition in the coniferous forests of CR represents 30–70% of the total deposition. The difference between coniferous (higher) and deciduous (lower) throughfall fluxes is significant because of the larger surface area of conifers and year-round exposure to air-borne sulphur. At several of the GEOMON sites, the flux of nitrogen via throughfall increased during the observation period and, at the end of the studied period (2000), nitrogen became the main source of acidification, replacing sulphur compounds. The highest fluxes (81.7 kg N ha^-1 yr^-1)were measured in 2000 in the Orlické hory Mts., which provide an example of multiple causes of forest decline – the direct impact of air pollution, abundance of nitrogen, acidification and secondary stressors (weather changes, insect pests, fungal infections). A comparison is given with data from other countries.     

Elevational trends in the fluxes of sulphur and nitrogen in throughfall in the Southern Appalachian Mountains: Some surprising results

From 1986–1989, a team of scientists measured atmospheric concentrations and fluxes in precipitation and throughfall, and modeled dry and cloudwater deposition in a spruce-fir forest of the Great Smoky Mountains National Park which is located in the Southern Appalachian Region of the United States. The work was part of the Integrated Forest Study (IFS) conducted at 12 forests in N. America and Europe. The spruce-fir forest at 1740 m consistently received the highest total deposition rates (～2200, 1200, and 700 eq ha^?1 yr^?1 for SO₄ ^2?, NO₃ ^?, and NH₄ ⁺). During the summers of 1989 and 1990 we used multiple samplers to measure hydrologie, SO₄ ^2?, and NO₃ ^? fluxes in rain and throughfall events beneath spruce forests above (1940 m) and below (1720 m) cloud base. Throughfall was used to estimate total deposition using relationships determined during the IFS. Although the SO₄ ^2? fluxes increased with elevation by a factor of ～2 due to higher cloudwater interception at 1940 m, the NO₃ ^? fluxes decreased with elevation by ～30%. To investigate further, we began year round measurements of fluxes of all major ions in throughfall below spruce-fir forests at 1740 m and at 1920 m in 1993–1994. The fluxes of most ions showed a 10–50% increase with elevation due to the ～70 cm yr^?1 cloudwater input at 1920 m. However, total inorganic nitrogen exhibited a 40% lower flux in throughfall at 1920 m than at 1740 m suggesting either higher dry deposition to trees at 1740 m or much higher canopy uptake of nitrogen by trees at 1920 m. Differential canopy absorption of N by trees at different elevations would have significant consequences for the use of throughfall N fluxes to estimate deposition. We used artificial trees to understand the foliar interactions of N.     

Throughfall deposition of ammonium and sulphate during ammonia fumigation of a scots pine forest

The estimation of the dry deposition of sulphur dioxide to forests is confounded by the possibility of co-deposition of SO₂ with NH₃ on leaf surfaces. A sector of Scots pine forest was selectively fumigated with NH₃ to give average concentrations up to 15 ppbV (nL L^–1) above ambient, in order to test the hypothesis that increased air concentrations of NH₃ would enhance the dry deposition of SO₂, and the consequent amounts of SO₄ ^2– measured in throughfall below the forest canopy. Ammonia gas, generated by evaporation of concentrated aqueous solution, was released above the canopy in proportion to wind speed when the wind direction was between south and west. Concentrations of NH₃ at canopy height were measured using passive diffusion tubes; throughfall was preserved with thymol and measured weekly. Meteorological data and SO₂ concentrations were recorded continuously, to permit the estimation of dry deposition input. Deposition of NH₄ ⁺ in throughfall over 8 months was increased by up to 40 meq m^–2 relative to control sites upwind of the NH₃ release point, with largest values closest to the release point. Deposition of SO₄ ^2– in throughfall was also enhanced in the fumigated area, by up to 20 meq m^–2, even though average ambient SO₂ concentrations were 2.3 ppbV. The results are discussed in terms of the factors controlling SO₂ deposition on forest surfaces, the development of appropriate deposition models, and their relevance to using throughfall as an estimate of total S deposition.     

A canopy budget model to assess atmospheric deposition from throughfall measurements

A canopy exchange model is presented which allows atmospheric deposition to be estimated from longterm throughfall and precipitation measurements. For a forest in the Netherlands, the combination of throughfall measurements and this model resulted in deposition estimates which were similar to deposition estimates derived from micrometeorological measurements and inferential modeling, deposition of NOy being the only exception. Unfortunately, several basic assumptions in the canopy exchange model are not properly evaluated, which up to now limits its application. Suggestions are made on how the model can be improved.     

Nitrogen Deposition and Nitrate Leaching at Forest Edges Exposed to High Ammonia Emissions in Southern Bavaria

The atmospheric deposition of air pollutants was studied by means of monitoring canopy throughfall at six forest stands. The investigation was carried out in Norway spruce (Picea abies L. Karst.) forests in Southern Bavaria with high ambient ammonia concentrations due to either adjacent intensive agriculture or poultry housing. Five monitoring plots transected the forest edges and forest interior from the edge, at 50, 150, about 400 m and about 800m to the interior. Additionally, nutrient concentration in soil solution was sampled with suction cups at each plot, and C/N ratio of the humus layer was also determined. The variation of ambient ammonia concentration between three of the six investigated sites was estimated using diffusive samplers. In order to compare the effects of atmospheric deposition on European beech (Fagus sylvatica L.) and Norway spruce additional monitoring plotswere installed under each of these species in a mixed beech and spruce stand. Bulk deposition and soil water samples were analysed for major ions (NO₃ ^-, NH₄ ⁺, SO₄ ^2-, Cl^-, Na⁺, K⁺, Mg²⁺, Ca^2+M).The results show a substantial increase of deposition towards the forest edges for all ions. This so called 'edge effect' continued in most cases until a distance from 50 to 150 m from edge. For both ambient ammonia concentrations and nitrogen deposition, it can be concluded that increased dry deposition is the main reason for the edge effect. Over 76% of the nitrogen ratios in throughfall deposition between the edge and 50 m distance into the spruce forest exceed 1.0. Except for potassium, beech generally showed lower ratios than spruce.Due to high nitrogen deposition the forest floor, C/N ratios were lower at stand edges when compared to their interior. In contrast to the increase of nitrogen deposition at the edge, nitrate export below the main rooting zone was lower at the edge. Nitrate export was generally lower under beech than spruce. Nitrogen budgets of some plots were negative, indicating a reduction of total ecosystem nitrogen stock.The results show that forest edges, especially in areas with high air pollution, receive much more atmospheric deposition than the interior parts of closed forest stands. As many deposition studies in forests were conducted at field stations in the central parts of forests the estimated deposition for the whole forest may be underestimated. This may be important to consider in geo-statistical studies and models aiming to estimate spatial critical deposition values, especially with an increasing fragmentation of the forest cover.     

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.     

Ausfilterung von Schwefelverbindungen aus der Luft durch einen Buchenbestand

Filtering of Sulfur compounds from air by beech forest In a mature beech (Fagus silvatica) forest the amounts of sulfate-S per ha and year in open land precipitation, throughfall, stem flow and seepage in 100 cm soil depth have been measured from 1969 to 1976. From the fluxes measured quantitative data on plant leaching and dry deposition in the form of plant filtering are derived. Dry deposition amounts to 26kg S · ha^?1 · y^?1 and is of the same size as wet deposition (24 kg). The leaching of sulfate takes place only in autumn and amounts to ca. 3 kg S. The acid soil in the range of Al-buffering increases its sulfate storage annually by ca. 17 kg S/ha.     

An intensive 1-month investigation of trace metal deposition and throughfall at a mountain spruce forest

During July 1986, atmospheric concentrations and deposition rates of Ph, Cd, Zn, and Mn were measured at a spruce forest in the Great Smoky Mountains National Park, and meteorological data were recorded. Precipitation, cloud water impaction, and dry deposition were quantified. Average total fluxes of 12, 1.0, 53, and 40 µg m^?2 d^?1 for Pb, Cd, Zn, and Mn, respectively, were measured; dry deposition constituted 46, 32, 62 and 66% of each of the totals. Cloud impaction (unusually low for this particular month) was measurable but not quantitatively important. Dry deposited Pb and Zn were washed from the canopy by subsequent rainfall — revealing greater throughfall fluxes associated with increasing antecedent dry period durations. Cadmium and Mn did not, however, show this relationship. Measurements revealed little interaction of Cd with the forest canopy, while considerable net leaching of Mn was evident (as had been expected). The canopy behaviors of both Pb (i.e., leaching) and Zn (i.e., uptake) were contrary to expectations.     

Input of Atmospheric Particles into Forest Stands by Dry Deposition

In this study the dry input of atmospheric particles into a forest stand is quantified. A wash-off-method using the natural leaf surfaces as collectors of the dry deposition was chosen. The direct on-site-measurement on living branches were achieved in a spruce stand (Picea abies (L.) Karst) at Solling, Germany. The ion exchange processes occurring on natural branches can reliably be quantified through immediate sequential washings. In order to calculate also the gas dry deposition of those trace elements which occur in both particle and gas phases, a resistance model was used. From these results the deposition velocity of particulate aerosol components into the forest stand was calculated. Dry particle deposition constitutes an important part of the total matter input into the forest ecosystem. Just the nitrogen input into Solling only by dry deposition (from particle-, mist-, and gas-deposition) with about 30 kg N ha^?1 a^?1 already exceeds the critical load of 20 kg N ha^?1 a^?1 by far, and this is without even considering the additional load by wet deposition which amounts to 15 kg ha^?1 a^?1. These findings are of greatest ecological importance, as the damage to the stability of the forest ecosystem caused by increased nitrogen input is considerable. Only a quick and drastic reduction of sulphur and nitrogen emissions could stop the further increase of the nutritient imbalance and the progressing acidification of this ecosystem.     

Deposition of acidifying compounds in Sweden

The Swedish Environmental Research Institute (IVL) has monitored deposition of acidifying compounds in Sweden. The monitoring programmes were initiated by various air quality protection associations, and regional forest and environmental authorities. The purpose is to quantify sulphur (S) and nitrogen (N) deposition to forests, and to illustrate possible acidification of the soil. Actual deposition of S and N is compared with critical loads. Deposition is investigated by precipitation studies in open field areas and by throughfall studies in forest stands. Soilwater chemistry is examined in the forest stands and used as indication of soil conditions. For most of the study sites, data on needle loss, forest growth, and soil chemistry are available from the National Board of Forestry. All available data are combined in a computer database for evaluation. Evaluation of data during 1985–94 shows that regional deposition monitoring illustrates the size and distributional pattern of S and seasalts. Monitoring data can identify certain regions receiving heavy loads of N, which can be found mainly in southern Sweden. Soilwater analyses indicates that large areas in Sweden have heavily acidified forest soils, low pH-values, low levels of calcium (Ca²⁺), magnesium (Mg²⁺), and potassium (K⁺), and raised levels of inorganic aluminium (iAl). Forest sites in the coastal regions of southern and south-western Sweden also showed raised inorganic N levels in soilwater. The relationship between deposition load and effects on soil chemistry is recognised by a correlation between S deposition and iAl levels in soilwater. Another correlation was found between N deposition (throughfall) and N levels in soilwater.     

The role of organic horizons and canopy to modify the chemistry of acidic deposition in some forest ecosystems

To clarify the mechanisms of pH buffering in forest ecosystems, field observations of pH and ionic concentrations in precipitation (R), throughfall (Tf), stemflow (Sf), and leachates from organ c horizons (Lo) were conducted for three years at three stands in Tomakomai (TK) and Teshio (TS) in Hokkaido, northern Japan. Weighted mean rates of H⁺ input as wet deposition at TK and TS were estimated in the range from 0.3 to 1.0 and 0.4–0.6 kmol_c ha^?1 y^?, respectively. While the net H⁺ flux was reduced significantly by the forest canopy, net fluxes of other ions by throughfall, especially for Na⁺, Cl^?, and SO₄ ^2?, were apparently greater than those by precipitation. The canopy modification of the H⁺ flux was more remarkable under deciduous stands than under coniferous stands, suggesting that the efficiency of conifers as the collectors of dry deposition is greater than that of deciduous ones. More than 50% of H⁺ flux due to throughfall was absorbed by the organic horizons and the weighted mean pH of Lo at TK and TS was in the range from 4.9 to 5.5 and 5.0–5.5, respectively. Results from field observation and field leaching experiments, showed that the major H⁺ sinks of the organic horizons are exchange reaction of Ca²⁺, Mg²⁺ and K⁺. Organic acids or organo-metallic complexes of lower pK(=5.0–5.5) played a significant role as counter anions in O horizons leachate in coniferous forests. Our results indicate the importance of biogeochemical modifications in the canopy and organic horizon in acid buffering mechanisms of forest ecosystems.     

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.     

Spatial variability in nutrient deposition under an oak/beech canopy

Nutrient deposition in throughfall and stemflow were measured on a two-weekly basis in an oak/beech forest in the eastern part of the Netherlands. The large number of sampling points (11 throughfall and 8 stemflow collectors) enabled an analysis of the spatial variability in ion deposition. Spatial variability of ion depositions in throughfall revealed wide variation both between dissolved constituents as between seasons for single dissolved constituents. On a two weekly basis coefficients of variation ranged from 20–72% with highest values generally occurring for ortho-P and H and during spring. In contrast coefficients of variation based upon annual deposition totals ranged from 9–31%. Ion depositions in stemflow showed a much higher spatial variability with coefficients of variation for annual totals ranging from 46–115% with highest values again reported for ortho-P and H. The results on the ion-depositions in throughfall are summarized in a scheme in which for a given dissolved constituent and a desired accuracy interval, the needed number of sampling points is indicated.     

Effects of acidic deposition on soil ecosystems under forest in the Chongqing region of China

The effects of acidic deposition on soil ecosystems under temperate coniferous forest in the Chongqing region of China were investigated from 1993 to 1994. Precipitation, throughfall, stemflow, soil solutions, and soil samples were collected to estimate the acidification of soil ecosystems through the changes of their chemical components. The concentrations of ion species in the throughfall and stemflow under masson pine forest in Mt. Zhenwu were higher than those under mixed coniferous forest in Mt. Jinyun and under camphor tree forest in Laojundong, suggesting that Mt. Zhenwu is located in the vicinity of the Chongqing center and that it allowed the canopy of masson pine to intercept air pollutants. However, the level of aluminum dissolution into soil solutions was relatively low under masson pine forest in Mt. Zhenwu in spite of the low pH in the stemflow.     

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.     

Atmospheric sulfur deposition for a red soil broadleaf forest in southern China

A two-year study in a typical red soil region of Southern China was conducted to determine 1) the dry deposition velocity (Vd) for SO2 and particulate SO4^2- above a broadleaf forest, and 2) atmospheric sulfur fluxes so as to estimate the contribution of various fractions in the total. Using a resistance model based on continuous hourly meteorological data, atmospheric dry sulfur deposition in a forest was estimated according to Va and concentrations of both atmospheric SO2 and particulate SO2^4-. Meanwhile, wet S deposition was estimated based on rainfall and sulfate concentrations in the rainwater. Results showed that about 99% of the dry sulfur deposition flux in the forest resulted from SO2 dry deposition.In addition, the observed dry S deposition was greater in 2002 than in 2000 because of a higher average concentration of SO2 in 2002 than in 2000 and not because of the average dry deposition velocity which was lower for SO2 in 2002. Also,dry SO2 deposition was the dominant fraction of deposited atmospheric sulfur in forests, contributing over 69% of the total annual sulfur deposition. Thus, dry SO2 deposition should be considered when estimating sulfur balance in forest ecological systems.