Effect of Chronic Nitrogen Additions on Soil Nitrogen Fractions in Red Spruce Stands

The responses of temperate and boreal forest ecosystems to increased nitrogen (N) inputs have been varied, and the responses of soil N pools have been difficult to measure. In this study, fractions and pool sizes of N were determined in the forest floor of red spruce stands at four sites in the northeastern U.S. to evaluate the effect of increased N inputs on forest floor N. Two of the stands received 100 kg N ha^-1 yr^-1 for three years, one stand received 34 kg N ha^-1 yr^-1 for six years, and the remaining stand received only ambient N inputs. No differences in total N content or N fractions were measured in samples of the Oie and Oa horizons between treated and control plots in the three sites that received N amendments. The predominant N fraction in these samples was amino acid N (31-45% of total N), followed by hydrolyzable unidentified N (16-31% of total N), acid-soluble N (18-22% of total N), and NH₄ ⁺ (9^-13% of total N). Rates of atmospheric deposition varied greatly among the four stands. Ammonium N and amino acid N concentrations in the Oie horizon were positively related to wet N deposition, with respective r2 values of 0.92 and 0.94 (n = 4, p < 0.05). These relationships were somewhat stronger than that observed between atmospheric wet N deposition and total N content of the forest floor, suggesting that these pools retain atmospherically deposited N. The NH₄ ⁺ pool may represent atmospherically deposited N that is incorporated into organic matter, whereas the amino acid N pool could result from microbial immobilization of atmospheric N inputs. The response of forest floor N pools to applications of N may be masked, possibly by the large soil N pool, which has been increased by the long-term input of N from atmospheric deposition, thereby overwhelming the short-term treatments.     

Studies of Atmospheric Nitrogen Deposition in a Mire of the German National Park Hochharz Mountains Using Two Different Methods

The purpose of this study was to determine the nitrogen (N) deposition in a mire of the German National Park Hochharz Mountains in regard to different input pathways of open area and forest stand deposition. High N deposition rates strongly affect the development and growth of mires in general. For determination of the open area N deposition two methods were applied: the bulk deposition method and the Integral Total Nitrogen Input (ITNI) method. This method is based on the ¹⁵N isotope dilution technique and was adapted at this study to evaluate its applicability for natural ecosystems as well as to compare with the traditional bulk method. The forest stand deposition included canopy throughfall, stemflow and fog was measured by means of bulk collectors. On the test site, bulk deposition measurements showed an input of 27 kg N ha^{? 1} yr^{? 1} in the open area and 47 kg N ha^{? 1} yr^{? 1} in the forest stand. The higher N input in the forest stand is caused by interception of fog by the canopy. N concentrations in fog were up to more than six times higher than in rain. The ITNI system yielded a total N deposition of 30 kg N ha^{? 1} yr^{? 1} on average in the open area. The small differences between the two simultaneously applied measuring techniques were caused by a minimum biomass development of the autochthonous plant Calamagrostis villosa in the ITNI system. With increasing biomass production the influence of plants on the atmospheric N input also increased. It can be concluded that the ITNI system is beneficial for the application in a natural ecosystem when using more robust and biomass producing plants. The measured atmospheric N deposition exceeds the critical load for nutrient poor mires and represents therefore a potential risk for the continuity of this ecosystem.     

Average critical loads for nitrogen and sulfur and its use in acidification abatement policy in the Netherlands

Atmospheric deposition of N and S on terrestrial and aquatic ecosystems causes effects induced by eutrophication and acidification. Effects of eutrophication include forest damage, NO₃ pollution of groundwater and vegetation changes in forests, heathlands and surface waters due to an excess of N. Effects of acidification include forest damage, groundwater pollution, and loss of fish populations due to Al mobilization. Critical loads (deposition levels) for N and S on terrestrial and aquatic ecosystems in the Netherlands related to these effects have been derived by empirical data and steady-state acidification models. Critical loads of N generally vary between 500 and 1500 mol _c ha^?1 yr^?1 for forests, heathlands and surface waters and between 1500 and 3600 for phreatic groundwaters. Critical loads of total acid (S and N) vary between 300 to 500 mol _c ha^?1 yr^?1 for phreatic groundwaters and surface waters and between 1100 to 1700 mol ha^?1 yr^?1 for forests. On the basis of the various critical loads a deposition target for total acid of 1400 mol _c ha^?1 yr^?1 has been set in the Netherlands from which the N input should be less than 1000 mol _c ha^?1 yr^?1. This level, to be reached in the year 2010, implies an emission reduction of 80–90% in SO₂, NO _x and NH₃ in the Netherlands and of about 30% in neighboring countries compared to 1980 emissions.     

Influence of acid deposition on element cycling in mature sugar maple forest,Algoma, Canada

Forestry studies were undertaken within the Turkey Lakes Watershed to determine the impact of long-range transport of air pollutants on biogeochemical processes in old-growth sugar maple forest on shallow Precambrian-derived till soils in the Algoma District of Ontario, Canada. Distributions of organic matter and macroelements were determined in the tree- and field-layer vegetation, the forest floor and the mineral soil of the study site. Annual tree growth was largely offset by mortality, resulting in a relatively stable standing stock of ca. 245 t ha^?1. Annual aboveground litter production averaged 3.7 t ha^?1 yr^?1, chiefly in the form of deciduous leaf fall. The average pH of the precipitation (4.3) was reduced considerably by contact with the forest canopy. Throughfall was enriched with other elements, principally K and, to a lesser extent, Ca and Mg. The cationic composition of the forest-floor percolates, on the other hand, was dominated primarily by Ca and only to a lesser extent by Mg and K. The stand receives moderate acid deposition, mainly from average inputs of 33–36 kg ha^?1 yr^?1 of SO₄ ^2? and 24–29 kg ha^?1 yr^?1 of NO₃ ^? distributed throughout the year. Atmospheric inputs add to substantial natural NO₃ ^? production, notably within the forest floor and upper mineral soil, and contribute to leaching of bases, principally Ca and Mg, from the rooting zone. Active recycling of elements together with weathering of primary minerals should assist in preserving the base status of the site.     

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.     

Proton Budget for a Japanese Cedar Forest Ecosystem

The proton budget for a Japanese cedar (Cryptomeria japonica) forest in Gunma Prefecture, Japan, was studied by estimating biogeochemical fluxes. The proton budgets were estimated for three individual compartments of the ecosystem: vegetation canopy, and the upper (O horizon + 0–10 cm) and lower (10–100 cm) soil layers. The dominant proton sources in the compartments were atmospheric deposition (1.2 kmol ha^?1 yr^?1), nitrification (5.1 kmol, ha^?1 yr^?1) and base-cation uptake by vegetation (8.0 kmol, ha^?1 yr^?1) respectively. These proton sources were neutralized almost completely within the individual compartments mainly by base-cation release from the canopy or the soil. The sum of internal proton sources was five times as large as that of external ones. Nitrogen input from the atmosphere was 2.2 kmol ha^?1 yr^?1, whereas its output from the lower soil layer was 3.9 kmol ha^?1 yr^?1, indicating that a net loss of nitrogen occurred in the ecosystem. However, this did not cause the acidification of soil leachates because of a sufficient release rate of base cations from the soil.     

Estimation of the Maximum Critical Load for Sulfur in South Korea

The maximum critical load of sulfur and its exceedance by the sulfur deposition of 1994–1997 were mapped for South Korea with a spatial resolution of 11 × 14 km using the steady-state mass balance method. The Korean soil and geological maps were used as basis for the estimations of the critical alkalinity leaching and the weathering rate of base cations. The normalized difference vegetation index data obtained from the Advanced Very High Resolution Radiometer (AVHRR) together with the observed primary productivity of plants were used for the estimation of the critical uptake of base cations. Wet deposition of the non-sea-salt base cations was derived from measured base cation concentrations in precipitation, precipitation rate and air concentration of total suspended particulate while dry deposition of base cations was estimated using the inferential technique using scavenging ratios. The predominant ranges of base cation weathering, uptake and deposition were estimated to be of 200 – 600 eq ha^?1 yr^?1, 200 – 400 eq ha^?1 yr^?1 and 400 – 600 eq ha^?1 yr^?1, respectively. Critical alkalinity leaching was mainly in the range of 1000 – 2000 eq ha^?1 yr^?1 due to relatively high value of precipitation runoff. Exceedance of sulfur critical load was found at 40 % of the ecosystems considered mainly in the southeastern part of Korea, and about 60 % of Korea ecosystems were sustainable against sulfur acidity loadings.     

Comparison of two methods to assess the carbon budget of forest biomes in the Former Soviet Union

The sink of CO₂ and the C budget of forest biomes of the Former Soviet Union (FSU) were assessed with two distinct methods: (1) ecosystem/ecoregional, and (2) forest statistical data. The ecosystem/ecoregional method was based on the integration of ecoregions (defined with a GIS analysis of several maps) with soil/vegetation C data bases. The forest statistical approach was based on data on growing stock, annual increment of timber, and FSU yield tables. Applying the ecosystem/ecoregional method, the area of forest biomes in the FSU was estimated at 1426.1 Mha (10⁶ ha); forest ecosystems comprised 799.9 Mha, non-forest ecosystems and arable land comprised 506.1 and 119.9 Mha, respectively. The FSU forested area was 28% of the global area of closed forests. Forest phytomass (i.e., live plant mass), mortmass (i.e., coarse woody debris), total forest plant mass, and net increment in vegetation (NIV) were estimated at 57.9 t C ha^?1, 15.5 t C ha^?1, 73.4 t C ha^?1, and 1.0 t C ha^?1 yr^?1, respectively. The 799.9 Mha area of forest ecosystems calculated in the ecosystem/ecoregional method was close to the 814.2 Mha reported in the FSU forest statistical data. Based on forest statistical data forest phytomass was estimated at 62.7 t C ha^?1, mortmass at 37.6 t C ha^?1; thus the total forest plant mass C pool was 100.3 t C ha^?1. The NIV was estimated at 1.1 t C ha^?1 yr^?1. These estimates compared well with the estimates for phytomass, total forest plant mass, and NIV obtained from the ecosystem/ecoregional method. Mortmass estimated from the forest statistical data method exceeded the estimate based on the ecosystem/ecoregional method by a factor of 2.4. The ecosystem/ecoregional method allowed the estimation of litter, soil organic matter, NPP (net primary productivity), foliage formation, total and stable soil organic matter accumulation, and peat accumulation (13.9 t C ha^?1, 125.0 t C ha^?1, 3.1 t C ha^?1 yr^?1, 1.4 t C ha^?1 yr^?1, 0.11, and 0.056 t C ha^?1 yr^?1, respectively). Based on an average value of NEP (net ecosystem productivity) from the two methods, and following a consideration of anthropogenic influences, FSU forests were estimated to be a net sink of approximately 0.5 Gt C yr^?1 of atmospheric C.     

An update of the mercury inventory and atmospheric mercury fluxes to and from Finland

Finland, the northern-most agricultural/industrial country in the world, has been for some time steadily improving environmental mercury (Hg) research. This paper focuses upon Hg recovery during zinc production, uses of Hg, updating of information on Hg emissions and atmospheric transport of Hg to and from Finland. The recovery of Hg as a by-product of zinc production began in 1970. The highest amount of recovered Hg was noted to be 160 t in 1989. Total uses of Hg in different sectors were about 7.4 t in 1992, which had decreased by 50% since the year 1987. In 1992, the estimated Hg emission to air was 2 t yr^?1, whereas to water and land the emission was about 0.20 and 3.67 t yr^?1, respectively. Natural Hg emission in Finland was estimated to be about 0.4 t yr^?1 (range: 0.3 to 0.5 t yr^?1). In addition, an initial attempt was made to estimate the atmospheric Hg flux to and from Finland; these values were noted to be 2.7 and 2.1 t yr^?1, respectively.     

Critical deposition levels for nitrogen and sulphur on dutch forest ecosystems

Critical loads for N and S on Dutch forest ecosystems have been derived in relation to effects induced by eutrophication and acidification, such as changes in forest vegetation, nutrient imbalances, increased susceptibility to diseases, nitrate leaching, and Al toxicity. The criteria that have been used are N contents in needles, nitrate concentrations in groundwater (drinking water), and NH₄/K ratios, Ca/Al ratios, and Al concentrations in the soil solution. Assuming an equal contribution of N and S, all effects seem to be prevented at a total deposition level below 600 mol_c ha^?1 yr^?1 due to N uptake by stemwood and acid neutralization by base cation weathering. The most serious effects will probably be prevented at total deposition levels between 1500 and 2000 mol_c ha^?1 yr^?1. The current average deposition in the Netherlands is 4900 mol_c ha^?1 yr^?1.     

Potential hazards of lime application in a damaged pine forest ecosystem in Berlin,Germany

Ninety percent of the pines (P. Sylvestris) in the forests of Berlin (West) are classified as damaged. Needle and leaf analyses do not indicate nutrient deficiencies. In site of high S-inputs (55 kg ha^?1 yr^?1 with throughfall) total acid inputs are moderate (2.4 kmol ha^?1 yr^?1) due to their neutralization by carbonatic dusts. Heavy metal depositions have led to accumulations in the forest floor (e.g. Pb 150 mg kg^?1, Cd 0.5 mg kg^?1). The dominating soil type, a cambic arenosol (Ustipsamment) is strongly acidified (pH 3.2 – 4.0) and poor in available nutrients. On an experimental plot, the application of dolomitic lime (6.1 tons ha^?1) and fertilizer (145 kg ha^?1 K₂SO₄) led to a significant increase m pH and base saturation in the top 10 cm of the mineral soil after 2 yr. The data on element fluxes give evidence for increased mineralization rates, enhanced heavy metal accumulation in the forest floor and increased soil solution concentrations of potentially hazardous substances (Al, Cd, NO₃). The lime application is discussed in terms of site specific effects on ecosystem stability and groundwater quality.     

Acidification of Nova Scotia Lakes

Although water chemistry of precipitation and lakes in Nova Scotia is dominated by C1 from sea salt, correction for marine influence reveals that the dominant anion in acidified lakes is SO₄. Atmospheric deposition of non-marine SO₄ (SO₄) and NO₃- for the period 1977–1980 at 4 stations in southwest Nova Scotia averaged 47 meq SO₄ ^* m^?2 yr^?1 and 21 meq NI₃-m^?2 yr^?1 compared with 38 and 13 meq, respectively, for the average of 3 stations in the northeastern third of the province. Precipitation pH increased from 4.5 to 4.8 along the same axis. Almost 50% of the SO₄ deposition occurred when storms came from the southwest, indicating low pressure tracks which pass south of major Canadian sources of S. SO₄ ^* deposition in metropolitan Halifax (1982 bulk data) was 87 meq m^?2 yr^?1, due to local emissions of ca. 28 300 tonne S in the area, as well as LRTAP. Concurrent deposition of NO₃-N was 15 meq m^?2 yr^?1 (2.1 kg ha^?1 yr ^?1). Loadings from SO₄ deposition in the Halifax area amount to 42 kg ha^?1 yr^?1 and clearly exceed the federal guideline (M.O.I., 1983) of 20 kg ha^?1 yr^?1. Water chemistry of southwest, northeast, and Halifax area lakes show the same general SOI trends as observed for atmospheric deposition. In addition we find a positive relationship between SOI concentrations in the urban lakes and proximity to the center of the urban area.     

Effects of nitrogen deposition on the acidification of terrestrial and aquatic ecosystems

The concentration of ammonium and nitrate in precipitation has increased during this century. The deposition of N compounds (wet + dry) is reaching 30 to 40 kg ha^?1yr^?1 in many areas in Central Europe and above 20 kg in the southern parts of Scandinavia. In extreme situations throughfall data indicate depositions above 60 kg ha^?1yr^?1 in Central Europe and above 40 kg ha^?1yr^?1 in south Sweden. Very high depositions are observed on slopes at forest edges and adjacent to areas with animal farms and manure spreading. In areas with low N deposition almost all deposited N (>95%) will be absorbed in the tree canopies or in the soil. In areas with high deposition an increased outflow is observed which in some cases reach 10 to 15 kg ha-lyr-1. The increased output is an indication of N saturation of the ecosystem and it leads to acidification effects in soils, soilwater, groundwater and surface waters.     

Calculating critical loads of acid deposition with PROFILE — A steady-state soil chemistry model

A steady state soil chemistry model was used to calculate the critical load of acidity for forest soils and surface waters at Lake GÄrdsjön in S.W. Sweden. The critical load of all acid precursors (potential acidity) for the forest soil is 1.64 kmol_c ha^?1 yr^?1, and 1.225 kmol_c ha^?1 yr^?1 for surface waters. For the most sensitive receptor, the critical load is exceeded by 1.0 kmol_c ha^?1 yr^?1, and a 80% reduction in S deposition is required, if N deposition remains unchanged. The critical load is largely affected by the present immobilization of N in the terrestrial ecosystem which is higher than the base cation uptake. The model, PROFILE, is based on mass balance calculations for the different soil layers. From measurable soil properties, PROFILE reproduces the present stream water composition as well as present soil solution chemistry. The model calculates the weathering rate from independent geophysical properties such as soil texture and mineral composition.     

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.     

Ion leaching from a sugar maple forest in response to acidic deposition and nitrification

Year-to-year variation in acidic deposition within a mature sugar maple-dominated forest and in leaching of ions from the associated podzolic soil were examined at the Turkey Lakes Watershed between 1981 and 1986. Below-canopy inputs to the soil of SO₄ ^2? and NO₃ ^? in throughfall averaged 640 and 295 eq. ha^?1 yr^?1; the corresponding ranges were 493–917 and 261–443 eq. ha^?1 yr^?1. The contribution of atmospheric deposition to SO₄ ^2? NO₃ ^? and Ca²⁺ leaching decreased over the six years. During the study period, the mean annual volume-weighted NO₃ ^? concentration decreased in throughfall and forest-floor percolate and increased in the mineral-soil solution collected below the effective rooting zone. A substantial shift in the balance between SO₄ ^2? and NO₃ ^?leaching from the mineral soil was observed; leaching of SO₄ ^2?decreased and NO₃ ^? leaching increased with time. Leaching of Ca²⁺ and Mg²⁺ from the soil was increased as a result of excess NO₃ ^? production in the soil. The calculated output of NO₃ ^? from the soil, which averaged 1505 eq. ha^?1 yr^?1, considerably exceeded the atmospheric deposition of NO₃ ^?, whereas SO₄ ^2? outputs were only moderately greater than inputs.     

Trace element release from forest floor can be monitored by ion exchange resin tubes

Risk assessment of heavy metal input into forest ecosystems requires information about metal fluxes from the forest floor (organic layer) into the mineral soil. Common methods for the monitoring of element fluxes are generally time‐consuming and expensive. Additionally, the reliability of the results is in part contested especially for trace elements, showing very low concentrations which are sometimes even below analytical detection limit. We used ion exchange resin tubes installed below the forest floor to determine heavy metal and As fluxes at 25 forest monitoring sites in Germany. Chloride tracer experiments and the comparison of our data with throughfall and lysimeter data, determined within the Level II monitoring network, proved the accuracy of our method. Mean trace element fluxes based on the resin method were 50 g As ha^–1 yr^–1, 2 g Cd ha^–1 yr^–1, 168 g Cu ha^–1 yr^–1, 176 g Ni ha^–1 yr^–1, and 186 g Pb ha^–1 yr^–1.The results show that the organic layer may change into a source of heavy metals after emission has decreased.     

Ozone Sensitivity Differences in Five Tomato Cultivars: Visible Injury and Effects on Biomass and Fruits

A complete record derived from the core from the Daihai Lake in a remote area provides new insights into the changing atmospheric heavy metal deposition associated with historical industrial activities, the Asian monsoon, long-range transport, and the chemical composition of matter derived from weathering of catchment. The fluctuation of lithogenic element concentration in the lake sediments can readily be explained by a particle sorting effect induced by the Asian monsoon. The variation of atmospheric deposition of Cu and Pb shows a similar profile in the lower part of the core sediments, and coincides with environmental change, with high atmospheric deposition coupled with wet, temperate period; while low deposition with dry, cold period, indicating a transport variation of heavy metal pollutants entrained by the Asian summer monsoon. From the beginning of nineteenth century, the atmospheric deposition of Cu and Pb decreased and then slowly increased. This may be associated with the destroyed industry induced by long-term wars in China and the less heavy metal pollutants relative to the weak Asian summer monsoon in this period. Comparison between atmospheric-derived metal and sediment trap metal using Ga as the reference element shows that atmospheric Cu and Pb budgets do not exceed the fluvially-induced Cu and Pb budgets in the indirectly disturbed area. On average, there have been approximately 5.4 mg m^?2 yr^?1 of Cu and 5.1 mg m^?2 yr^?1 of Pb atmospherically deposited in the region.     

Atmospheric deposition to grassland canopies: Lysimeter budgets discriminating between interception deposition,mineral weathering and mineralization

Lysimeter experiments were used to determine atmospheric input to grassland canopies. The combined effect of interception deposition + mineral weathering + mineralization was calculated from input/output budgets. Four types of lysimeters were used, either filled with very pure quartz sand or chalk grassland soil, and either without vegetation or planted with Brachypodium pinnatum (L.) Beauv., Combination of budgets for these four types of lysimeters yielded separate estimates of interception deposition and mineral weathering + mineralization. Ratios between total deposition and bulk deposition were 1.74 and 1.93 for N and S, respectively. Sources and sinks of H⁺ for lysimeters with chalk grassland soil and planted with Brachypodium (abbrev. CP-lysimeters) were about 10 times larger than for lysimeters without plants and filled with quartz sand. The contribution of atmospheric input to total H⁺-sources was 80% for bare lysimeters filled with quartz sand, and only 12% for CP-lysimeters. Bulk deposition and total atmospheric deposition of N was 1.25 and 2.18 kmol ha^?1 yr^?1, respectively, whereas N mineralization of chalk grassland soil yielded 1.62 kmol ha^?1 yr^?1, ‘Acid rain’ has only a minor influence on H⁺-transformations within a chalk grassland ecosystem, but N cycling is seriously affected by atmospheric input.     

Critical loads for nitrogen deposition on forest ecosystems

Critical loads for N deposition are derived from an ecosystem's anion and cation balance assuming that the processes determining ecosystem stability are soil acidification and nitrate leaching. Depending on the deposition of S, the parent soil material, and the site quality critical N deposition rates will range between 20 to 200 mmol m^?2 yr^?1 (3 to 14 kg ha^?1 yr^?1) on silicate soils and reach 20 to 390 mmol m^?2 yr^?1 (3 to 48 kg ha^?1) on calcareous soils.