Atmospheric sulfur and nitrogen in West Java

Wet-only rainwater composition on a weekly basis was determined at four sites in West Java, Indonesia, from June 1991 to June 1992. Three sites were near the extreme western end of Java, surrounding a coal-fired power station at Suralaya. The fourth site was ～100 km to the east in the Indonesian capital, Jakarta. Over the 12 months study period wet deposition of sulfate at the three western sites varied between 32–46 meq m^?2 while nitrate varied between 10–14 meq m^?2. Wet deposition at the Jakarta site was systematically higher, at 56 meq m^?2 for sulfate and 20 meq m^?2 for nitrate. Since sulfate and nitrate wet deposition fluxes in the nearby and relatively unpopulated regions of tropical Australia are both only ～5 meq m^?2 anthropogenic emissions of S and N apparently cause significant atmospheric acidification in Java. It is possible that total acid deposition fluxes (of S and N) in parts of Java are comparable with those responsible for environmental degradation in acid-sensitive parts of Europe and North America.     

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.     

Rainwater Composition and Acidity at Five Sites in Malaysia, in 1996

Rainwater chemical composition and acidity were determinedfrom weekly-averaged wet-only rainwater samples collected atfive sites in Malaysia throughout 1996. The major aim of thiswork was to assess the extent to which acid deposition, foundpreviously at one site in the Klang Valley, was a general,rather than local, phenomenon. To this end, three measurementsites were located spanning the length of the Klang Valley (anurban-industrial region of approximately 3000 km²containing the Malaysian capital, Kuala Lumpur). A fourth sitewas located outside, but adjacent to the Klang Valley, and thefinal site was located 300 km to the southeast, in anurban/industrial region adjacent to Singapore. Annual pHvalues in the range 4.16–4.40 and estimated total depositionfluxes of acidic sulfur and nitrogen species in the range 120–350 meq m^-2 yr^-1 show all sites to be impactedsignificantly by acidic deposition. Average contributionswere 60% as sulfur species, 40% as nitrogen species. Theresults confirm that potentially significant levels of aciddeposition occur in Malaysia as a regional phenomenonassociated with urban/industrial activities.     

Deposition of acidic species at a rural location in New South Wales,Australia

Wet-only rainwater composition on a daily basis, and atmospheric SO₂ and NO₂ concentrations on a monthly basis have been measured over a two year period at four sites ～100 km to the west of Sydney. Bulk aerosol composition on a monthly basis was also measured at one site. The study region is predominantly rural in character, but contains two coal-fired thermal power stations with a total installed capacity of 2320 MW, as well as several min or population centres, including a small city, with a total population of about 21,000. The measurement sites were located roughly on the perimeter of a circle of about 20 km radius having the power stations at its centre. Three of the sites were situated in rural settings, while the fourth was located on the outskirts of the small city of Lithgow. Atmospheric acid loadings at all sites were low by the standards usually associated with industrialised regions of Europe and North America, with about one third of rainwater total acidity provided by organic acids (formic, acetic and oxalic). At the three rural sites, total inorganic acid deposition, comprising measured wet deposition plus inferred dry deposition of acidic S and N species, averaged about 30 meq m^?2 y^?1, a low figure by most standards. At the site located near the city of Lithgow total deposition of acidic S and N species averaged about 80 meq m^?2 y^?1.     

Phosphorus and potassium fertility of some riceland soils in Indonesia

Abstract

Contents of soil phosphorus and potassium vary appreciably in different localities of the Indonesian Archipelago. Data collected for riceland soils from seven irrigation areas (five on Java and one each on Sumatra and Sulawesi) show that average available phosphorus contents in the tilled layer may range from 23 ppm P at the Sumatra location to 203 ppm Pat the Sulawesi location. Average exchangeable potassium contents ranged from less than 0.2 meq/100g. K in the Sumatran soils to over 1.0 meq/100g. in potash‐rich soils of Java. Distinct regional differences in soil fertility of the magnitude observed indicate that blanket fertilizer recommendations cannot be made if rice production is to be increased without wasting chemical fertilizers which are relatively scarce and expensive in Indonesia. Increased emphasis must be placed on soil testing and soil fertility research in order to achieve the national goal of self‐sufficiency in food stuffs.     

The Prediction of Nitrate Leaching with the First-Order Acidity Balance (FAB) Model for Upland Catchment in Great Britain

The relative contribution of N deposition to the acidification of freshwaters in Great Britain has increased over the last few years as S deposition has fallen in line with reduced emissions. In certain high deposition areas of Great Britain, NO₃ ^--based acidity can equal or exceed the contribution of SO₄ ^2--based acidity in some upland waters. Here we apply the first-order acidity balance model (FAB) to predict the maximum N leaching from 13 study catchments at future steady state. Using mean water chemistry and catchment soils data, along with long-term default values for N sink processes, we predict NO₃-N leaching at much higher rates than currently are being measured in surface waters, with a mean increase of 10.5 kg ha^-1 yr^-1. As a result, mean acid neutralizing capacity would decline to less than 0 meq L^-1 at 4 sites. While there are uncertainties associated with model parameterization relating to the short-term storage of N within catchment soils and vegetation, model outputs do indicate much greater leaching of N at some time in the future as steady-state is achieved.     

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.     

Ion mass budgets for small forested catchments in Finland

Ion mass and H⁺ budgets were calculated for three pristine forested catchments using bulk deposition, throughfall and runoff data. The catchments have different soil and forest type characteristics. A forest canopy filtering factor for each catchment was estimated for base cations, H⁺, Cl^? and SO ₄ ^2? by taking into account the specific filtering abilities of different stands based on the throughfall quality and the distribution of forest types. Output fluxes from the catchments were calculated from the quality and quantity of the runoff water. Deposition, weathering, ion exchange, retention and biological accumulation processes were taken into account to calculate catchment H⁺ budgets, and the ratio between external (anthropogenic) and internal H⁺ sources. In general, output exceeded input for Na⁺, K⁺, Ca²⁺, Mg²⁺, HCO ₃ ^? (if present) and A^? (organic anions), whereas retention was observed in the case of H⁺, NH ₄ ⁺ , NO ₃ ^? and SO ₄ ^2? . The range in the annual input of H⁺ was 22.8–26.3 meq m^?2 yr^?1, and in the annual output, 0.3–3.9 meq m^?2 yr^?1. Compared with some forested sites located in high acid deposition areas in southern Scandinavia, Scotland and Canada, the catchments receive rather moderate loads of acidic deposition. The consumption of H⁺ was dominated by base cation exchange plus weathering reactions (41–79 %), and by the retention of SO ₄ ^2? (17–49 %). The maximum net retention of SO ₄ ^2? was 87% in the HietajÄrvi 2 catchment, having the highest proportion of peatlands. Nitrogen transformations played a rather minor role in the H⁺ budgets. The ratio between external and internal H⁺ sources (excluding net base cation uptake by forests) varied between 0.74 and 2.62, depending on catchment characteristics and acidic deposition loads. The impact of the acidic deposition was most evident for the southern Valkeakotinen catchment, where the anthropogenic acidification has been documented also by palaeolimnological methods.     

Sulfur Deposition in Asia: Seasonal Behavior and Contributions from Various Energy Sectors

Sulfur transport and deposition in Asia, on an annual andseasonal basis, is analyzed using the ATMOS model. Calculationsare performed for two complete years (1990 and 1995). Deposition amounts in excess of 0.5 g S m^-2 yr^-1 are estimated for large regions in Asia, with values as high as 10 g S m^-2 yr^-1 in southeastern China. Annual averaged SO₂ concentrations in excess of 20 μg SO₂ m^-3 are calculated for many urban and suburban areas ofeastern China and S. Korea, with an average of 5 μg SO₂ m^-3 over most of the emitter regions. Sulfur deposition by major source categories is also studied. Southeast Asia (Indonesia, Malaysia, Philippines, Singapore)receives ～25% of its sulfur deposition from shipping activities. Sulfur deposition from bio-fuel burning is significant for most of the underdeveloped regions in Asia. Volcanoes are a major source of sulfur emissions in the PacificOcean, Papua New Guinea, Philippines and Southern Japan. Sulfur deposition is shown to vary significantly throughout the year.The monsoons are found to be the largest factor controlling sulfur transport and deposition in the Indian sub-continent andSoutheast Asia. India receives over 35% of its total depositionduring the summer months. In East Asia, sulfur deposition isestimated to be 10% higher during summer and fall than winterand spring. Model results are compared with observations from a number of monitoring networks in Asia and are found to be generally consistent with the limited observations.     

Weekly Measurements over One Year of Ammonia Concentrations and Surface Exchange Fluxes at a Danish Heathland with Passive Wind-Vane Flux Samplers in an Aerodynamic Gradient Configuration

The present study aims to establish the annual NH₃ deposition to an inland heathland in Denmark using a micro-meterological approach with passive wind-vane flux samplers. The integrating samplers were replaced at weekly intervals from May 1995 to May 1996. The average concentration, 2.05 μg m^-3 at the heathland is at a moderate level when compared to heathlands in other parts of Europe. The average deposition velocity was 0.83 cm s^-1 which is within the range of depositon velocities found for other heathlands in Europe. The average canopy resistance was found to be relatively high, 61 s ^-1. The measurements yielded a total NH₃-N deposition of 2.4 (± 0.9) kg ha^-1 yr^-1 with a data coverage of 71% for 1995/1996. In 40% of this time the flux is regarded as zero because the flux is not significant different from zero. In 60% of this time the significant fluxes varied from –0.052 μg m^-2 s^-1 (deposition equal 16.4 kg N ha^-1 yr^-1) to 0.089 μg m^-2 s^-1 (emission equal 28.2 kg N ha^-1 yr^-1). The method is only able to direct measure significant fluxes down to the equivalence of 0.010 μg m^-2 s^-1 (approximately 3.2 kg ha^-1 yr^-1). Therefore the exact deposition cannot be determined by the applied method at very low deposition sites such as a coastal heathland in Denmark. In a high-deposition area as in the central Netherlands the method gave significant fluxes with a 100% data coverage for a two month period.     

Effects of Reduced S Deposition on Large-Scale Transport of Sulphur in Swedish Rivers

Sulphur deposition has diminished by about half during the last decade. For Sweden consistent estimates of total deposition are available for 1991, and 1994–97. Based on these estimates and using GIS the deposition for large drainage areas during one decade are calculated. These values are compared with the measured S transport in rivers covering about 85% of the Swedish territory, thus enabling the construction of a S budget for Sweden. The majority of the drainage areas have a net loss of S, which can be attributed to desorption of S in the soil. During the period of high deposition in the 1980:s (>60 meq m^?2 yr^?1 in southern Sweden) S was adsorbed, and retarded acidification. There still seems to be some S-adsorption in the northern parts of the country, where the deposition is less (now <20 meq m^?2 yr^?1).     

The cation denudation rate as a quantitative index of sensitivity of eastern Canadian rivers to acidic atmospheric precipitation

A model has been developed that relates the cation denudation rate (CDR) of a watershed (the rate that cations derived from chemical weathering are carried off by runoff), the atmospheric load of excess SO₄, and the pH of the river. Chemical and discharge data for rivers in Nova Scotia and Newfoundland were used to develop and test the model, which is based upon the common major ion chemistry of soft surface waters, and may be expressed by three statements: (1) CDR (meq m^?2 yr^?1) ? Excess SO₄ ^?? load (meq m^?2 yr^?1) = HCO₃ ^? (meq m^?2 yr^?1), (2) HCO₃ ^? (meq m^?2 yr^?1)/Runoff (m³ m^?2 yr^?1) = HCO₃ ^? (meq m^?3), (3) pH = pK + \(pP_{CO_2 } \) ? pHCO₃ ^?. The model in concentration form applies well to lakes. A detailed analysis of the data for the Isle aux Morts River, Newfoundland, is presented, showing that the CDR varies throughout the year, affected by both discharge and seasonal pattern.     

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.     

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.     

Deposition Patterns of SO4 2−, NO3 − and H+ in the Brazilian Territory

SO₄ ^2?, NO₃ ^? and H⁺ depositions are estimated in the Brazilian territory based on the existing rainfall chemical data and on annual rainfall distribution over the whole territory. Local and regional depositions are estimated. Rainfall chemical data over the Braziliian territory shows that the average pH values are usually low (between 4.0 and 5.5). These values are observed in the tropical Amazon forest as well as in urban areas. However, the rainwater acidity in the tropical forests are due to organic acids naturally produced by the vegetation while in urban areas the acidity is mainly due to acidic anion deposition (NO₃ ^? and SO₄ ^2?). In some Amazonian areas, the average input values through rainfall for NO₃ ^? is about 0.06 keq.ha.yr^?1 and for SO₄ ^2? is between 0.23 and 0.54 keq.ha^?1.yr^?1. On the other hand, in some urban centers, such as São Paulo, values of .072 keq.ha^?1.yr^?1 for NO₃ ^? and 1.16 keq.ha^?1.yr^?1 of SO₄ ^2? are found and in sites where sulfate sources (coal mining) are present, as for the area of Florianópolis, values as high as 5.59 keq.ha^?1.yr^?1 for SO₄ ^2? are found.     

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.     

Regionalization of critical loads under uncertainty

The steady-state model PROFILE was used to perform Monte Carlo simulations of critical loads of acidity and exceedances of forest soils for 128 sites in the province of Scania, southern Sweden. Statistical tests showed that 100 sites had normal distributed critical loads and exceedances and that the variance of these parameters was statistically equal for all sites. Pooled estimates of the standard deviation was 0.19 and 0.31 kmol_c ha^?1 yr^?1 for the critical loads and exceedances, respectively. Introduction of uncertainties, expressed as confidence intervals, in the cumulative distribution function for critical loads showed that overlaps between percentiles were substantial. The 5%-ile was systematically equal to the 57%-ile using a 67% confidence interval and equal to the 87%-ile when a 95% confidence level was chosen. The overlaps of percentiles cause a reduction of acidic deposition according to the mean value of the 5%-ile to protect only 68% of the ecosystem area with an 84% probability and not a guaranteed protection of 95% as if uncertainties did not exist. Thus, uncertainties make it possible to advocate reductions to levels of deposition below the 5%-tile of critical loads.     

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.     

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.