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

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

Changes in water quality in the Laflamme Lake Watershed Area,Canada

The Laflamme Lake Watershed Area is located in a sensitive region on the Canadian Shield and is subjected to wet atmospheric loading between 17 and 25 kg ha^?1 yr^?1. From 1981 to 1988, the level and fluctuations of the atmospheric deposition of acidifying substances has led to various responses in the water chemistry of headwater lakes in the area. The general trend in atmospheric inputs is a gradual increase of acidifying substances from 1981 to 1985 followed by a 2 yr decrease then a return to previous values. In the two lakes with almost no alkalinity acidification has occured throughout the 1983 to 1988 period. In the four lakes with slightly higher alkalinity values, a reversal in acidification is seen when atmospheric loading decreased in 1986. Along with the interannual trends, seasonal variability to acidification occurs with sensitivity of surface waters being highest during spring melt. Sensitivity to acidification can also be altered by watershed processes and in the Laflamme Lake Watershed, soil processes are effective in altering the acidity of precipitation before it reached the lake. In this watershed, wet atmospheric inputs of H⁺ and NO₃ ^? are larger than surface water outputs while the reverse occurs for Ca²⁺, Mg²⁺, Na⁺, K⁺, Cl^? and SO₄ ^2?.     

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.     

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.     

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.     

Assessment of critical loads and their exceedance on Dutch forests using a multi-layer steady-state model

Critical acid loads for Dutch forests were derived using a multi-layer steady-state model that includes canopy interactions, nutrient cycling, mineral weathering and N transformations. Values were calculated for combinations of 12 tree species and 23 soil types for a 10×10 km grid. Critical acid loads thus derived increased with decreasing soil depth. Nearly 90% of the values varied approximately between 1500 and 4000 mol_c ha^?1 yr^?1 at 10 cm soil depth and between 750 and 2000 mol_c ha^?1 yr^?1 at the bottom of the rootzone. Separate critical loads calculated for N and S at the bottom of the rootzone varied between approximately 300 and 1000 mol_c ha^?1 yr^?1 for N and between 150 and 1250 mol_c ha^?1 yr^?1 for S. Using deposition data of 1990, a median reduction of the deposition by approximately 75% was calculated to achieve the critical loads at the bottom of the rootzone. The overall uncertainty in this value was estimated to be about 10%, although it can be much larger for specific soil types such as clay and peat soils. For N a larger reduction deposition percentage was calculated than for S, especially for coniferous forests with a high present N input.     

Acidity neutralization mechanism in a forested watershed in Central Japan

The contributions of cation exchange and mineral weathering to the neutralization of acidity in the Jingahata watershed in central Japan were estimated through a laboratory weathering experiment and runoff chemistry measurements. The laboratory experiment was conducted in a stirred-flow reactor for a whole soil sample collected from the C horizon in the watershed. The concentration ratios of base cations (Ca²⁺, Mg²⁺, K⁺ and Na⁺) to Si (BC/Si) released during the steady-state stage of the laboratory experiment were in good agreement with the ratios of the net flux of base cations to the flux of Si in the streamwater (BC _{N ET}/Si _L).This result suggests that the acidity in the watershed is neutralized primarily by mineral weathering without causing a net loss of base cations from exchange sites. The alkalinity/acidity balance estimated for the watershed shows that the total weathering rate of base cations is approximately 3.26 keq ha^?1 yr^?1. Weathering of plagioclase (An₄₁) contributes 83% of the total weathering rate. The dominant acidity source is CO₂ released within the soil horizons, accounting for roughly 85% of the total acidity flux (3.20 keq ha^?1 yr^?1). This high internal production of acidity suppresses the relative importance of atmospheric acidity inputs (0.3 keq ha^?1 yr^?1).     

A Single Law to Describe Atmospheric Nitrogen Bulk Deposition versus Rainfall Amount: Inputs at the Seine River Watershed Scale

Atmospheric nitrogen species (NH₄-N and (NO₃+NO₂)-N) were determined in weekly samples of atmospheric bulk deposition (dry plus wet), collected in France at seven sites over the course of a year. Rural, semi-rural and industrialised-urban sites were chosen in the Seine river watershed from the Seine estuary to upstream from Paris. Mean NH₄-N concentrations varied from 0.7 to 1.7 mg L^-1. Mean (NO₃+NO₂)-N concentrations were approximately 0.5 mg L^-1 for all sites except Paris (0.7 mg L^-1), which has a local impact on the fallout contamination from urban emissions. The relation between concentration and rainfall amount obeys a power law, in the form of y = ax ^b. When the nitrogen sources are very local, this relationship turns into a dilution law. Annual atmospheric nitrogen deposition (NH₄-N+(NO₃+NO₂)-N) was calculated and varied from 7.8 kg ha^-1 yr^-1 in the neighbourhood of a rural town to 17.3 kg ha^-1 yr^-1 in a very industrialised harbour. 58% of the atmospheric nitrogen deposition occurred during ‘spring + summer’ period. The total nitrogen atmospheric input to the Seine estuary, via direct deposition + indirect input via the watershed, was estimated to about 5% of the total nitrogen load within the Seine river basin.     

Watershed vs in-lake alkalinity generation: A comparison of rates using input-output studies

As a means of assessing the relative contributions of watershed (terrestrial) and in-lake processes to overall lake/watershed alkalinity budgets, alkalinity production rates for watersheds and low alkalinity lakes were compiled from the literature and compared. Based on net alkalinity production data, derived using wet or bulk deposition data, mean and median alkalinity production for 20 watersheds in North America and Europe were 89 and 69 meq m^?2 yr^?1 (range 20 to 235 meq m^?2 yr^?1). For a subset of 10 watersheds with dry deposition data, terrestrial alkalinity production neutralized an additional 35 meq m^?2 yr^?1 of acidic deposition. For 11 lakes, mean and median in-lake alkalinity generation were 99 and 88 meq m^?2 yr^?1 (range 22 to 240 meq m^?2 yr^?1). Analysis of data indicates that for the low alkalinity systems described here, areal alkalinity production rates for watersheds and lakes are approximately equal. This relationship suggests that watershed area to lake area ratio can be used as a convenient estimator of the relative importance of watershed and in-lake sources of alkalinity for drainage lake systems. For precipitation-dominated seepage lakes and other systems where hydrology limits soil-water contact, hydrologic flow paths and residence times can be of overriding importance in determining alkalinity sources. For regions dominated by drainage lakes with high watershed area to lake area ratios (such as the Northeastern U.S.), however, alkalinity budgets are dominated by watershed processes. Omission of in-lake alkalinity consideration for most lakes in such regions would have little impact on computed alkalinity budgets or on predicted response to changes in acidic deposition loadings.     

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.     

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.     

Relations between lake acidification and sulfate deposition in Northern Minnesota,Wisconsin, and Michigan

From a level of 1 kg ha^?1yr^?1 in north central Minnesota, emission-related wet SO₄ deposition increases across northern Wisconsin and northern Michigan to about 18 kg ha^?1yr^?1 in south central Michigan. Samples taken from 82 clearwater (low color) lakes across this region in the summer of 1984 showed a pattern of acidification in proportion to deposition. We found a linear increase in the difference between alkalinity and Ca+Mg and in lake SO₄ concentration with increasing deposition. We developed a simple equation to predict the emission-related SO₄ deposition levels that will cause the alkalinity of sensitive clear-water lakes to go to zero.     

A comparison of the effects of sediments and standard elutriates on phosphorus kinetics in lakewater

Average rates of atmospheric deposition of total phosphorus (TP) and total nitrogen (TN) to Narrow Lake, located on sedimentary bedrock in the boreal forest of central Alberta, were 20 and 424 mg m^?2 yr^?1, respectively, between 1983–1986. There were no significant differences (P > 0.05) in deposition rates between sites on Narrow Lake, on the lake shore, and on land 18 km away. Deposition of TP, but not TN, followed a distinct pattern during the open-water season; TP was highest just after ice-off (May) and decreased throughout the remainder of the open-water season. Deposition during the winter accounted for only 4 and 12% of the annual TP and TN loads, respectively. Dry fallout contributed 50 and 33% of atmospheric deposition of TP and TN, respectively. In both dry and wet fallout, dissolved P (< 0.45 μm) and organic N were the predominant fractions of TP and TN, respectively. During July 1986, unusually heavy rainfalls caused an increase in TP, but not TN, concentrations in the epilimnion of Narrow Lake. Wet fallout accounted for only 9% of the observed increase of epilimnetic TP; the rest was from surface runoff from the drainage basin. The design of sampling programs to measure atmospheric deposition of nutrients to lakes is discussed.     

Dry and wet atmospheric deposition of nitrogen, phosphorus and silicon in an agricultural region

We measured atmospheric nutrient deposition as wet deposition and dry deposition to dry and wet surfaces. Our analyses offer estimates of atmospheric transport of nitrogen (N), phosphorus (P) and silicon (Si) in an agricultural region. Annual dry and wet deposition (ha^?1 year^?1) was 0.3 kg of P, 7.7 kg of N, and 6.1 kg of Si; lower than or similar to values seen in other landscapes. N:P and Si:N imply that atmospheric deposition enhances P and Si limitation. Most P and soluble reactive P (SRP) deposition occurred as dryfall and most dry-deposited P was SRP so would be more readily assimilable by plant life than rainfall P. Dry deposition of N to wet surfaces was several times greater than to dry surfaces, suggesting that ammonia (NH _x ) gas absorbtion by water associated with wet surfaces is an important N transport mechanism. Deposition of all nutrients peaked when agricultural planting and fertilization were active; ratios of NH _x :nitrate (NO _x ) hbox{reflected} the predominant use of NH _x fertilizer. Wet deposition estimates were consistent over hundreds of km, but dry deposition estimates were influenced by animal confinements and construction. Precipitation wash-out of atmospheric nutrients was substantial but larger rain events yielded higher rates of wet deposition. Methodological results showed that local dust contaminated wet deposition more than dry; insects, bird droppings and leaves may have biased past deposition estimates; and estimating dry deposition to dry plastic buckets may underestimate annual deposition of N, especially NH _x .     

Long-term nitrogen balance for pearl millet (Pennisetum glaucum L.) in an acid sandy soil of Niger

On acid sandy soils of Niger (West Africa) fertilizer N recovery by pearl millet (Pennisetum glaucum L.) is often more than 100 per cent in years with normal or above average rainfall. Biological nitrogen fixation (BNF) by N₂-fixing bacteria may contribute to the N supply in pearl millet cropping systems. For a long-term field experiment comprising treatments with and without mineral fertilizer (F) and with and without crop residue application (CR) a N balance sheet was calculated over a period of six years (1983-1988). After six years of successive millet cropping total N uptake (36-77 kg N ha^?1 yr^?1) was distinctly higher than the amount of fertilizer N applied (30 kg N ha^?1 yr^?1). The atmospheric input of NH₄-N and NO₃-N in the rainwater was about 2 kg N ha_?1 yr^?1, 70 % in the form of NH₄-N. Gaseous NH₃ losses from urea (broadcast, incorporated) were estimated from other experiments to amount to 36 % of the fertilizer N applied. Nitrogen losses by leaching (15 to > 25 kg N ha^?1 yr^?1) were dependent on the treatment and on the quantity and distribution of single rainfall events (>50 mm). Decline in total soil N content (0-60 cm) ranged from 15 to 48 kg N ha^?1 yr^?1. The long-term N balance (1983-1988) indicated an annual net gain between 6 (+CR-F) and 13 (+CR+F) kg N ha^?1 yr^?1. For the control (-CR-F) the long-term N balance was negative (10 kg N ha^?1 yr^?1). In the treatment with crop residues only, the N balance was mainly determined by leaching losses, whereas in treatments with mineral fertilizer application the N balance depended primarily on N removal by the millet crop. The annual net gain in the N balance increased from 7 kg ha^?1 with mineral fertilizer to 13 kg ha^?1 in the combination mineral fertilizer plus crop residues. In both the rhizosphere and the bulk soil (0-15 cm), between 9 and 45% of the total bacterial population were N₂-fixing (diazotrophic) bacteria. The increased N gain upon crop residue application was positively correlated with an increase in the number of diazotrophic and total bacteria. The data on bacterial numbers suggest that the gain of N in the longterm N balance is most likely due to an N input by biological nitrogen fixation. In addition, evidence exists from related studies that the proliferation of diazotrophs and total bacteria in the rhizosphere due to crop residue application stimulated root growth of pearl millet, and thus improved the phosphorus (P) acquisition in the P deficient soil.     

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.     

N-Source Effects on Temporal Distribution of NO3-N Leaching Losses to Subsurface Drainage Water

Understanding the temporal distribution of NO₃-N leaching losses from subsurface drained ‘tile’ fields as a function of climate and management practices can help develop strategies for its mitigation. A field study was conducted from 1999 through 2003 to investigate effects of the most vulnerable application of pig manure (fall application and chisel plow), safe application of pig manure (spring application and no-tillage) and common application of artificial nitrogen (UAN spring application and chisel plow) on NO₃-N leaching losses to subsurface drainage water beneath corn (Zea mays L.)–soybean (Glycine max L.) rotation systems as a randomized complete block design. The N application rates averaged over five years ranged from 166 kg-N ha^?1 for spring applied manure to 170 kg-N ha^?1 for UAN and 172 kg-N ha^?1 for fall applied manure. Tillage and nitrogen source effects on tile flow and NO₃-N leaching losses were not significant (P?<?0.05). Fall applied manure with CP resulted in significantly greater corn grain yield (10.8 vs 10.4 Mg ha^?1) compared with the spring manure-NT system. Corn plots with the spring applied manure-NT system gave relatively lower flow weighted NO₃-N concentration of 13.2 mg l^?1 in comparison to corn plots with fall manure-CP (21.6 mg l^?1) and UAN-CP systems (15.9 mg l^?1). Averaged across five years, about 60% of tile flow and NO₃-N leaching losses exited the fields during March through May. Growing season precipitation and cycles of wet and dry years primarily controlled NO₃-N leaching losses from tile drained fields. These results suggest that spring applied manure has potential to reduce NO₃-N concentrations in subsurface drainage water and also strategies need to be developed to reduce early spring NO₃-N leaching losses.     

A simple dose-effect model of lake acidity in Québec (Canada)

A simple dose-effect model expressing the relationships between lake acidity, weighted mean annual sulfate concentration in wet deposition, Ca, Mg and true color (as an index of organic anion concentration) is presented. The agreement between observed and estimated pH for more than a 1000 lakes is high according to the Pearson coefficients of correlation (0.81 to 0.90) and the standard error of estimation (0.22 to 0.27 pH unit). Results obtained with this model show that an airborne sulfate target loading of 20 kg ha^?1 yr^?1 would be too high to adequately protect sensitive lake ecosystems. A target loading of 15 kg ha^?1 yr^?1 in wet deposition would be best suited for the protection of the greater portion of sensitive lakes. However, a target loading of 10 kg ha^?1 yr^?1 would be required to protect the most sensitive lake ecosystems.     

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.     

Nutrient fluxes from a soil treatment process for pig slurry

Abstract. The effects of pig slurry applications to a hydrologically isolated field treatment plant (at Solepur) were studied over a period of eight years. Thirty repeated doses, averaging 160 m³ ha^?1 were applied from April to October of each year (1991–1995), to reach a total application of 4930 m³ ha^?1. All slurry samples were analysed for their total solids (TS), macronutrient (C, N, P, K, Ca) and micronutrient (Cu, Zn) content. In total, 284 tonnes of total solids (57 t TS ha^?1 yr^?1), 115 tonnes of carbon (23 t C ha^?1yr^?1), 24.5 tonnes of nitrogen (4900 kg N ha^?1 yr^?1), 7964 kg of phosphorus (1593 kg P ha^?1 yr^?1), 16 518 kg of potassium (3304 kg K ha^?1 yr^?1), 183 kg copper (37 kg Cu ha^?1 yr^?1) and 266 kg zinc (53 kg Zn ha^?1 yr^?1) were applied to the soil. Thus, this site provides an opportunity to assess the balance and to examine the long‐term behaviour of nutrients under conditions of intensive land application of pig slurries or similar effluents. The main nutrient fluxes through the soil‐water system were determined for each element. Over 40% of the total carbon applied was retained by the soil. About 25% of the slurry nitrogen applied remained in the soil profile and 12.5% was leached through the drainage water as nitrate. Most of the slurry phosphorus applied was retained in the soil profile either as P‐Dyer extractable (83%), or as total soil phosphorus (112%); <0.01% was found in the drainage water. Forty‐three per cent of the potassium applied in the slurry was recovered from the soil profile and 15% was recovered in the drainage water. Most of the copper (62%) and zinc (74%) applied in the slurry remained in the soil as EDTA extractractable forms; very low percentages (0.05% and 0.6% respectively) were found in the drainage water.