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.     

The Behavior of Nitrogen Isotopes in Acidified Forest Soils in the Czech Republic

The effects of atmospheric deposition on N cycling in acidified soils were studied at three spruce and one beech forested sites in the Czech Republic. Nitrogen content and δ¹⁵N were monitored in bulk and throughfall precipitation, needles, leaves, soils and soil solutions. Changes in soil NO₃ ^- production, effect of admixing of atmospheric N in spruce forest and N consumption in deciduous forest are described using changes in ¹⁵N fractionation of mineralized N in soil. Admixing of atmospheric NH4+ can be identified at low concentrations of exchangeable NH₄ ⁺. The δ¹⁵N ratio of atmospheric NO₃ ^- input is on average by 2‰ less negative than the δ5N ratio in soil water; admixing changes the δ¹⁵N of soil NO₃ ^- detected in lysimeters.     

An Empirical Approach for Assessing the Relationship Between Nitrogen Deposition and Nitrate Leaching from Upland Catchments in the United Kingdom Using Runoff Chemistry

Samples were collected from 13 upland sites (main inflow and loch outflow) in the UK along an N deposition gradient of 12-50 kg ha^-1 yr^-1 to determine the relationship between N deposition and NO₃ ^- concentrations in surface waters. There was no direct correlation between NO₃ ^- leaching and soluble inorganic N deposition at these sites, but a significant relationship with NO₃ ^- was found using a deposition function incorporating dissolved organic carbon (DOC) flux from each catchment. A similar but less significant relationship was found between NO₃ ^- concentration and DOC:DON ratio in runoff water. Catchments showed evidence of N saturation, i.e., when mean NO₃ ^- concentration exceeded 5 µeq L^-1, when the mean DOC:DON ratio fell below an approximate value of 25. Five other large loch sites (LLS) with multiple subcatchments were used to test these relationships and for four of these mostly heathland sites the predicted NO₃ ^- concentrations closely matched measured values. At the fifth site, where most subcatchments were forested, the deposition function and DOC:DON ratios gave conflicting predictions and both methods generally underestimated measured NO₃ ^- concentrations. If the capacity of these catchments to retain deposited N is determined by C supply then many upland catchments in the UK may experience increasing NO₃ ^- concentrations in runoff in the future at current or increased levels of N deposition.     

Catchment-Scale Variation in the Nitrate Concentrations of Groundwater Seeps in the Catskill Mountains,New York,U.S.A.

Forested headwater streams in the Catskill Mountains of New York show significant among-catchment variability in mean annual nitrate (NO₃ ^-) concentrations. Large contributions from deep groundwater with high NO₃ ^-concentrations have been invoked to explain high NO₃ ^-concentrations in stream water during the growing season. To determine whether variable contributions of groundwater couldexplain among-catchment differences in streamwater, we measuredNO₃ ^- concentrations in 58 groundwater seeps distributed across six catchments known to have different annual average streamwater concentrations. Seeps were identified based on release from bedrock fractures and beddingplanes and had consistently lower temperatures than adjacentstreamwaters. Nitrate concentrations in seeps ranged from neardetection limits (0.005 mg NO₃ ^--N/L) to 0.75 mg NO₃ ^--N/L. Within individual catchments, groundwaterresidence time does not seem to strongly affect NO₃ ^-concentrations because in three out of four catchments therewere non-significant correlations between seep silica (SiO₂) concentrations, a proxy for residence time, andseep NO₃ ^- concentrations. Across catchments, therewas a significant but weak negative relationship betweenNO₃ ^- and SiO₂ concentrations. The large rangein NO₃ ^- concentrations of seeps across catchmentssuggests: 1) the principal process generating among-catchmentdifferences in streamwater NO₃ ^- concentrations mustinfluence water before it enters the groundwater flow system and 2) this process must act at large spatial scales becauseamong-catchment variability is much greater than intra-catchmentvariability. Differences in the quantity of groundwater contribution to stream baseflow are not sufficient to account for differences in streamwater NO₃ ^- concentrationsamong catchments in the Catskill Mountains.     

The impacts of atmospheric n inputs on throughfall,soil and stream water interactions for different aged forest and moorland catchments in Wales

A study of inorganic-N concentrations in streams, soil waters, throughfall and rainfall was conducted for one year in five moorland and 20 Sitka spruce plantation catchments in upland Wales. The forest ages ranged from 10 to 55 yr. Highly significant positive relationships with forest stand age existed for inorganic-N concentrations in streamwater, B and O horizon soil waters and throughfall. Inorganic-N in streams and B horizon waters was entirely NO₃ ^?. Inorganic-N fluxes in throughfall also showed a significant, positive relationship with stand age. Throughfall flux of inorganic-N in the oldest stand was 25.1 kgN ha^?1 yr^?1, double that in incident rainfall. The older forest stands appear unable to utilise the available N. Nitrification is very active in the soils of these older stands, resulting in significant soil acidification. The processes responsible for the observed NO₃ ^? leaching losses, and the implications for the debate on Nitrogen Critical Loads are discussed.     

Sources of acidity in forest-floor percolate from a maple-birch ecosystem

Ion concentrations in water collected within a forest of sugar maple and yellow birch at the Turkey Lakes Watershed near Sault Ste. Marie, Ontario were examined from 1982 to 1984 to determine sources of acidity and the extent of cation leaching from forest floor horizons. Volume-weighted concentrations and ion fluxes in throughfall and forest-floor percolate during the growing and dormant seasons were calculated. Hydrogen ion content of the forest-floor percolate decreased in relation to that of throughfall in the dormant season and increased in the growing season. Hydrogen ion deposition in throughfall could account for 100% of the flux of H⁺ through the forest floor in the dormant period, and 40% of the flux during the growing season. In forest-floor percolate, Ca²⁺ concentrations were positively correlated with those of SO₄ ^2-, NO₃ ^- and organic anions during both dormant and growing seasons. Sources of NO₃ ^- and organic anions within the ecosystem and major external inputs of NO₃ ^- and SO₄ ^2- were critical factors that influenced cation mobility in the forest floor.     

Retention and Leaching of Elevated N Deposition in a Forest Ecosystem with Gleysols

The responses of nitrogen transformations and nitrate (NO_{_3} ^-) leaching to experimentally increased N deposition were studied in forested sub-catchments (1500 m²) with Gleysols in Central Switzerland. The aim was toinvestigate whether the increase in NO₃ ^- leaching,due to elevated N deposition, was hydrologically driven orresulted from N saturation of the forest ecosystem.Three years of continuous N addition at a rate of 30 kgNH₄NO₃-N ha^-1 yr^-1 had no effects on bulksoil N, on microbial biomass N, on K₂SO₄-extractableN concentrations in the soil, and on net nitrification rates.In contrast, N losses from the ecosystem through denitrification and NO₃ ^- leaching increased significantly. Nitrate leaching was 4 kg N ha^-1yr^-1at an ambient N deposition of 18 kg N ha^-1 yr^-1.Leaching of NO₃ ^- at elevated N deposition was 8 kg Nha^-1 yr^-1. Highest NO₃ ^- leaching occurredduring snowmelt. Ammonium was effectively retained within theuppermost centimetres of the soil as shown by the absence ofNH₄ ⁺ in the soil solution collected with microsuction cups. Quantifying the N fluxes indicated that 80% ofthe added N were retained in the forest ecosystem.Discharge and NO₃ ^- concentrations of the outflow from the sub-catchments responded to rainfall within 30 min. The water chemistry of the sub-catchment outflow showed thatduring storms, a large part of the runoff from this Gleysol derived from precipitation and from water which had interactedonly with the topsoil. This suggests a dominance of near-surface flow and/or preferential transport through this soil. The contact time of the water with the soil matrix wassufficient to retain NH₄ ⁺, but insufficient for a complete retention of NO₃ ^-. At this site with soilsclose to water saturation, the increase in NO₃ ^- leaching by 4 kg N ha^-1 yr^-1 through elevated N inputsappeared to be due to the bypassing of the soil and the rootsystem rather than to a soil-internal N surplus.     

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.     

Sulphur and nitrogen input to the Ratanica forested catchment (Carpathian Foothills,southern Poland)

The study covers 1991–1994 concentrations of SO₂ and NO₂ in the air, concentrations of sulphur and nitrogen in bulk precipitation, throughfall and stemflow as well as input of S and N to the Ratanica forested catchment (S. Poland), which is exposed to moderate anthropogenic pollution are presented. There was high input of sulphur (26 kg ha^?1) and nitrogen (24 kg ha^?1) to the catchment, mainly in NH4⁺ (18 kg ha^?1). The significant contribution of NH₄ ⁺ connected with intensive agriculture in surrounding fields has led to eutrophication of the ecosystem.     

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.     

Fluxes and Trends of Nitrogen and Sulphur Compounds at Integrated Monitoring Sites in Europe

The International Cooperative Programme on Integrated Monitoring (ICP IM) is part of the effects monitoring strategy of the UN/ECE Convention on Long-Range Transboundary Air Pollution. We calculated input-output budgets and trends of N and S compounds, base cations and hydrogen ions for 22 forested ICP IM catchments/plots across Europe. The site-specific trends were calculated for deposition and runoff water fluxes and concentrations using monthly data and non-parametric methods. The reduction in deposition of S and N compounds, caused by the new Gothenburg Protocol of the Convention, was estimated for the year 2010 using atmospheric transfer matrices and official emissions. Statistically significant downward trends of SO₄, NO₃ and NH₄ bulk deposition (fluxes or concentrations) were observed at 50% of the ICP IM sites. Implementation of the new UN/ECE emission reduction protocol will further decrease the deposition of S and N at the ICP IM sites in western and northwestern parts of Europe. Sites with higher N deposition and lower C/N-ratios clearly showed an increased risk of elevated N leaching. Decreasing SO₄ and base cation trends in output fluxes and/or concentrations of surface/soil water were commonly observed at the ICP IM sites. At several sites in Nordic countries decreasing NO₃ and H⁺ trends (increasing pH) were also observed. These results partly confirm the effective implementation of emission reduction policy in Europe. However, clear responses were not observed at all sites, showing that recovery at many sensitive sites can be slow and that the response at individual sites may vary greatly.     

Examination of the Dissolved Inorganic Nitrogen Budget in Three Experimental Microbasins with Contrasting Land Cover—A Mass Balance Approach

A long-term hydrological and water chemistry research was conducted in three experimental microbasins differing in land cover: (1) a purely agricultural fertilized microbasin, (2) a forested microbasin dominated by Carpinus betulus (European hornbeam), and (3) a forested microbasin dominated by Picea abies (L.) (Norway spruce). The dissolved inorganic nitrogen (DIN: NH ₄ ⁺ , NO ₂ ^? , NO ₃ ^? ) budget was examined for a period of 3 years (1991–1993). Mean annual loads of DIN along with sulfate SO ₄ ^2? and base cations Ca²⁺, Mg²⁺, Na⁺, K⁺, and HCO ₃ ^? were calculated from ion concentrations measured in stream water, open-area rainfall, throughfall (under tree canopy), and streamwater at the outlets from the microbasins. Comparison of the net imported/exported loads showed that the amount of NO ₃ ^? leached from the agricultural microbasin is ～3.7 times higher (43.57 kg ha^?1?a^?1) than that from the spruce dominated microbasin (11.86 kg ha^?1?a^?1), which is a markedly higher export of NO ₃ ^? compared to the hornbeam dominated site. Our analyses showed that land cover (tree species) and land use practices (fertilization in agriculture) may actively affect the retention and export of nutrients from the microbasins, and have a pronounce impact on the quality of streamwater. Sulfate export exceeded atmospheric rainfall inputs (measured as wet deposition) in all three microbasins, suggesting an additional dry depositions of SO ₄ ^2? and geologic weathering.     

Fate of Nitrogen Compounds Deposited to Spruce (Picea Abies Karst.) and Pine (Pinus Silvestris L.) Forests Located in Different Air Pollution and Climatic Conditions

Measurements were made of NO₃-N and NH₄-N in bulk deposition, throughfall and soil solution on six permanent plots in pine and spruce stands located along a transect from the south to the north of Poland. Location differed both in the level of air pollution level and in climatic parameters. The total N load calculated from throughfall ranged from 12.5 to 34 kg^{-1a -1}. The load of NH₄-N exceeded the NO₃-N contribution. Differences in total N load were not reflected in foliar N concentration. Present forest health status of stands determined by defoliation class, and do not appear to be related to their N deposition.     

Synthesis of Nitrogen Pools and Fluxes from European Forest Ecosystems

To investigate which ecosystem parameters determine the risk and magnitude of nitrate leaching we compiled data from published and unpublished sources on dissolved inorganic nitrogen (DIN: NO₃ ^-) in throughfall, DIN leaching loss in runoff or seepage water, and other ecosystem characteristics from 139 European forests. Not all data were available for all sites: 126 sites had at least one year's data on DIN inputs and DIN leaching loss; 40-50 sites had some data on soil chemistry and/or vegetation pools of N. DIN inputs in throughfall range between <1 and about 70 kg N ha-1 yr-1 and the losses with seepage or runoff range between <1 and 50 kg N ha-1 yr-1. Retention of N within the ecosystem increases with increasing DIN deposition and increasing proportion of NH₄ ⁺ in deposition. The amount of N in needles and litterfall shows a significant linear relationship with throughfall deposition of DIN, whereas the C:N ratio of the organic (OH) horizon is uncorrelated to the level of throughfall-DIN flux. About 50% of the variability in DIN leaching loss can be explained by the flux of DIN in throughfall. Alternatively, about 60% of the variability in DIN leaching loss can be explained in a two-variable multiple regression combining the C:N ratio of the organic soil and the pH of the mineral soil. The survey data suggest that leaching of DIN from forest ecosystems in Europe is related in part to current DIN deposition and in part to the longer-term internal ecosystem N status as reflected in the chemistry of the humus and acidification status of the soil.     

Canopy and Soil Retention of Nitrogen Deposition in a Mixed Boreal Forest in Eastern Finland

Nitrogen deposition, leaching, and retention were monitored in a mature spruce (Picea abies Karsten) dominated mixed boreal forest in eastern Finland. Bulk precipitation, throughfall, stemflow, and percolation through the podzolic soil profile were monitored from 1993 to 1996. Mean annual bulk deposition of total N was 3.83 kg ha^-1, of which 33% was NH₄ ⁺, 26% was NO₃ ^- , and 41% was organic N. Throughfall+stemflow flux of total N was 2.93 kg ha^-1 yr^-1. Sixty-four % of NH₄ ⁺ and 38% of NO₃ ^- in bulk precipitation was retained by tre three canopy. Organic N was released (0.27 kg ha^-1 yr^-1) from the tree canopy. Nitrate-N was retained and organic N was leached as the water passed through the ground vegetation and soil O-horizon. Ammonium-N and organic N were retained mainly in the E-horizon. The output of total N from the E-horizon was only 5% of the total N deposition in the forest stand during the study period and it was mainly as organic N. The output of inorganic N forms from under B-horizon was seasonal and occurred mainly at spring snowmelt.     

Comparison of Nitrate Leaching under Silver Birch (Betula Pendula) and Corsican Pine (Pinus Nigra SSP. Laricio) in Flanders (Belgium)

In a forest in Flanders (Belgium), situated in a region of intensive livestock production, comparable stands of Corsican pine and silver birch were studied for (1) NH₄ ⁺ and NO₃ ^- concentrations in throughfall water and soil solution and (2) depositions and leaching of NH₄ ⁺ and NO₃ ^- to groundwater. In each stand, throughfall collectors and porous cup lysimeters at three depths (0.1m, 0.5m and 1m) were installed in three replicated sets. Throughfall concentrations of ammonium and nitrate were significantly different for both species as well as soil solution concentrations of nitrate at all depths. Under pine, nitrate concentrations of the soil solution at 1m depth clearly exceeded the Belgian critical level for drinking water (50 mg.1^-1). Under birch, this level was only sporadically exceeded. During the sampling period, the depositions of NH₄ ⁺-N and NO₃ ^--N reached respectively 21.6 kg/ha and 6.3 kg/ha under birch and 81.3 and 15.2 kg/ha under Corsican pine. Nitrate-N leaching under silver birch amounted 25.4 kg/ha whereas 56.4 kg/ha was measured under Corsican pine.     

山西省太原市旱作农区大气活性氮干湿沉降年度变化特征

鉴于大气氮素沉降对整个生态系统的重要影响,我国近年来陆续开展了不同尺度的大气氮素干、湿沉降的研究,但少有农业区多年连续监测的资料。本研究利用DELTA系统、被动采样器和雨量器在山西省太原市郊区阳曲县河村旱作农业区进行了4年的监测试验,观测大气氮素干、湿沉降的时间变异。结果表明:2011年4月—2015年3月,河村4年大气活性氮NH_3、HNO_3、NO_2、颗粒态NO_3~-(pNO_3~-)、颗粒态NH_4~+(pNH_4~+)平均沉降量分别为4.50 kg(N)·hm~(-2)·a~(-1)、3.54 kg(N)·hm~(-2)·a~(-1)、2.56 kg(N)·hm~(-2)·a~(-1)、1.62 kg(N)·hm~(-2)·a~(-1)、2.75 kg(N)·hm~(-2)·a~(-1),大气氮素干沉降总量为12.38~18.95 kg(N)·hm~(-2)·a~(-1),以2011年的氮干沉降量最高,2014年的最低。2011年4月—2015年3月各月氮干沉降量与氨气沉降量之间存在显著正相关,相关系数在0.809 8~0.937 1,由此可知,该地区活性氮沉降主要受农业氨气排放的影响。河村4年雨水中NO_3~-、NH_4~+平均浓度分别为3.20 mg(N)·L~(-1)和2.43 mg(N)·L~(-1),大气氮素湿沉降11.67~41.31 kg(N)·hm~(-2)·a~(-1)。年度间氮素湿沉降存在很大差异,以2012年氮素年湿沉降量最高,2014年最低,每年大气氮素湿沉降占氮总沉降量的份额超过50%。此外,4年湿沉降中不仅NO_3~--N和NH_4~+-N之间、且二者与降雨量也呈显著线性或二次相关关系,说明降雨量对NO_3~--N和NH_4~+-N的湿沉降影响较大。本研究表明太原市旱作农区不同年份间氮素湿沉降比干沉降差异更大,且总沉降数量较高。虽然是旱作区,该地区氮素干沉降略低于湿沉降。研究结果为该地区农田氮肥施用和氮素循环监测提供了理论依据。     

Contribution of dissolved organic nitrogen deposition to nitrogen saturation in a forested mountainous watershed in Tsukui, Central Japan

Nitrogen (N) budget was estimated with dissolved inorganic N (DIN) and dissolved organic N (DON) in a forested mountainous watershed in Tsukui, Kanagawa Prefecture, about 50 km west of Tokyo in Central Japan. The forest vegetation in the watershed was dominant by Konara oak (Quercus serrata) and Korean hornbeam (Carpinus tschonoskii), and Japanese cedar (Cryptomeria japonica). Nitrate (NO₃ ^?) concentration in the watershed streamwater was averagely high (98.0 ±± 19 (±± SD, n = 36) μmol L^?1) during 2001–2003. There was no seasonal and annual changes in the stream NO^? ₃ concentration even though the highest N uptake rate presumably occurred during the spring of plant growing season, a fact indicating that N availability was in excess of biotic demands. The DON deposition rates (DON input rates) in open area and forest area were estimated as one of the main N sources, accounting for about 32% of total dissolved N (TDN). It was estimated that a part of the DON input rate contributed to the excessive stream NO^? ₃ output rate under the condition of the rapid mineralization and nitrification rates, which annual DON deposition rates were positively correlated with the stream NO₃ ^? output rates. The DON retention rate in the DON budget had a potential capacity, which contributed to the excessive stream NO^? ₃ output rate without other N contributions (e.g. forest floor N or soil N).     

Input-Output Budgets of Inorganic Nitrogen for 24 Forest Watersheds in the Northeastern United States: A Review

Input-output budgets for dissolved inorganic nitrogen (DIN) are summarized for 24 small watersheds at 15 locations in the northeasternUnited States. The study watersheds are completely forested, free of recent physical disturbances, and span a geographical region bounded by West Virginia on the south and west, and Maine on the north and east. Total N budgets are not presented; however, fluxes of inorganic N in precipitation and streamwater dominate inputs and outputs of N at these watersheds. The range in inputs of DIN in wet-only precipitation from nearby National Atmospheric Deposition Program (NADP) sites was 2.7 to 8.1 kg N ha^-1 yr^-1 (mean = 6.4 kg N ha^-1 yr^-1; median = 7.0 kg N ha^-1 yr^-1). Outputs of DIN in streamwater ranged from 0.1 to 5.7 kg N ha^-1 yr^-1 (mean = 2.0 kg N ha^-1 yr^-1; median = 1.7 kg N ha^-1 yr^-1). Precipitation inputs of DIN exceeded outputs in streamwater at all watersheds, with net retention of DIN ranging from 1.2 to 7.3 kg N ha^-1 yr^-1 (mean = 4.4 kg N ha^-1 yr^-1; median = 4.6 kg N ha^-1 yr^-1). Outputs of DIN in streamwater were predominantly NO₃-N (mean = 89%; median = 94%). Wet deposition of DIN was not significantly related to DIN outputs in streamwater for these watersheds. Watershed characteristics such as hydrology, vegetation type, and land-use history affect DIN losses and may mask any relationship between inputs and outputs. Consequently, these factors need to be included in the development of indices and simulation models for predicting 'nitrogen saturation' and other ecological processes.     

Trends in the Chemistry of Acidified Bohemian Lakes from 1984 to 1995: I. Major Solutes

Temporal changes in major solute concentrations in six Czech Republic lakes were monitored during the period 1984–1995. Four chronically-acidic lakes had decreasing concentrations of strong-acid anions (C_SA = SO₄ ^2- + NO^{3 -} + Cl^-), at rates of 3.0 to 9.0 μeq L^-1 yr^-1. Decreases in SO₄ ^2-, NO₃ ^-, and Cl^- (at rates up to 5.1 μeq L^-1 yr^-1, 3.2 μeq L^-1 yr^-1, and 0.6 μeq L^-1 yr^-1, respectively) occurred. The response to the decrease in deposition of S was rapid and annual decline of SO₄ ^2- in lake water was directly proportional to SO₄ ^2- concentrations in the acidified lakes. Changes in NO₃ ^- concentrations were modified by biological consumption within the lakes. The decline in C^SA was accompanied in the four most acidic lakes by decreases in Al_T, increases in pH at rates of 0.011 to 0.016 pH yr^{- 1}, and decreases of Ca²⁺ and Mg²⁺ (but not Na⁺) in three lakes. The acid neutralizing capacity (ANC) increased significantly in all six lakes. Increases in base cation concentrations (CB = Ca²⁺ + Na⁺ + Mg²⁺ + K⁺) were the principal contributing factor to ANC increases in the two lakes with positive ANC, whereas decrease in C_SA was the major factor in ANC increases in the four chronically-acidic lakes. The continued chemical recovery of these lakes depends on the uncertain trends in N deposition, the cycling of N in the lakes and their catchments, and the magnitude of the future decrease in S deposition.