Chemical Characterization of Acid Fog and Rain in Northern Japan Using Back Trajectory and Oblique Rotational Factor Analysis

Fog/cloud and rain water were collected at the mountainside of Hachimantai range in northern Japan and rain water was also collected at Akita City in order to investigate the air pollutant scavenging mechanism. The concentrations of various ions in these samples were analyzed, and the fog drop size and the wind direction were measured at each fog event. The fog at Hachimantai range had a very high total ion concentration, and was considerably acidified by non sea salt (nss-) SO₄ ^2? and NO₃ ^?, compared with the rain at Akita and all sites in Hachimantai range. Using the oblique rotational factor analysis, three factors were extracted as the air pollutants; A: (NH₄)₂SO₄+H₂SO₄, B: sea salts+HNO₃+H₂SO₄, C: NH₄NO₃+OH^?. These salts are well-known as the cloud condensation nuclei (CCN). Combining the factor analysis with the 72h back trajectory at 850hPa level, the contribution of Factor A was closely connected to the long-range transportation of anthropogenic or natural aerosol in air masses of continental origin.     

Stability of Ionic Components in Precipitation Samples — A Case Study in Taipei

The changes in ionic contents were studied in acidic precipitation samples collected for precipitation events in Taipei, which is near the sea. The storage cases under investigation include filtration, refrigeration, and light. Thus the experimental design leads all precipitation samples collected in the same rain event stored under different conditions. They were then analyzed six times successively within two months to provide the information containing potential ionic composition change. The measured constituents are H⁺, K⁺, Na⁺, Ca²⁺, Mg²⁺, NH₄ ⁺, NO₃ ^?, SO₄ ^2?, and Cl^?. The comparison of measured ionic concentrations corresponding to different storage methods yield no significant difference. The increases of NO₃ ^? and decreases of NH₄ ⁺ with time were observed to be of similar magnitude, while the variation of pH values is significant. The presented study indicated the important role played by sample storage in determining the ionic composition of precipitation samples.     

Evalution of Acid Deposition in Korea

This study was carried out to evaluate acid depositions and to understand their effect. Wet precipitation has been collected at twenty-four sites in Korea for one year of 1999. The ion concentrations such as H⁺, Na⁺, K⁺, Mg²⁺, NH₄ ⁺, Ca²⁺, Cl^?, NO₃ ^? and SO₄ ^2? were chemically analyzed and determined. Precipitation had wide range of pH(3.5～8.5), and volume-weighted average was 5.2. The contribution amounts of Cl^?, SO₄ ^2? and NO₃ ^? in anion were shown to be 54%, 32%, and 14%, respectively and those of Na⁺ and NH₄ ⁺ in cation were 32% and 25%. The ratios of Cl^? and Mg²⁺ to Na⁺ in precipitation were similar to those of seawater, which imply that great amount of Cl^? and Mg²⁺ in precipitation could be originated from seawater. The concentration of H⁺ is little related with SO₄ ^2?, NO₃ ^? and Cl^? ions, whereas nss^?SO₄ ^2? and NO₃ ^? are highly correlated with NH₄ ⁺, which could suggest that great amount of SO₄ ^2? and NO₃ ^? exist in the form of ammonium associated salt. The annual wet deposition amounts (g m^?2year^?1) of SO₄ ^2?, NO₃ ^?, Cl^?, H⁺, NH₄ ⁺, Na⁺, K⁺, Ca²⁺ and Mg²⁺ were estimated as 0.88～4.89, 0.49～4.37, 0.30～9.80, 0.001～0.031, 0.06～2.15, 0.27～4.27, 0.10～3.81, 0.23～1.59 and 0.03～0.63.     

Long-Term Trends in the Chemical Composition of Precipitation over Western Japan

Wet deposition monitoring was conducted at six rural stations in western Japan, during the period from 1987 through 1996. Long-term trends in the concentration of non-sea salt ions were analyzed on the basis of the data obtained. The monitoring results indicated that annual average concentrations of NO₃ ^? and NH₄ ⁺ in precipitation significantly increased on the order of 45%, and that of nss-Ca²⁺ and nss-SO₄ ^2?, concentrations did not change over the past 10 years. The ratio of NO₃ ^?/nss-SO₄ ^2? in precipitation significantly increased, the ratio of NO₃ ^?/NH₄ ⁺ showed no marked fluctuations, and the ratio of [nss-Ca²⁺+NH₄ ⁺]/[nss-SO₄ ^2?+NO₃ ^?] slightly increased during the period. These findings suggested that the wet deposition of NO₃ ^? and NH₄ ⁺ in western Japan, particularly that in the winter season, was influenced by the long-range transport of nitrogen oxides and ammonia from the Asian continent.     

Chemical Composition of Precipitation, Throughfall and Soil Solutions at Two Forested Sites in Guangzhou, South China

Rain water at two forested sites in Guangzhou (south China) show high concentrations of SO₄ ^2?, NO₃ ^? and Ca²⁺ and display a remarkable seasonal variation, with acid rain being more important during the spring and summer than during the autumn and winter. The amount of acid rain represents about 95% of total precipitation. The sources of pollutants from which acid rain developed includes both locally derived and long-middle distance transferred atmosphere pollutants. The seasonal variation in precipitation chemistry was largely related to the increasing neutralizing capacity of base cations in rainwater in winter. Soil acidification is highlighted by high H⁺ and Al³⁺ concentrations in soil solutions. The variation in elemental concentration in soil solution was related to nitrification (H⁺, NH₄ ⁺ and NO₃ ^?) and cation exchange reaction (H⁺, Al³⁺) in soil. The negative effect of soil acidification is partly dampened by substantial deposition of base cations (Ca²⁺, Mg²⁺ and K⁺) in this area.     

Geographical and Temporal Variations of Chemical Constituents in Winter Precipitation Collected in the Areas along the Coast of the Sea of Japan

The geographical and temporal variations of chemical constituents in winter precipitation collected in the areas along the coast of the Sea of Japan (AASJ) were discussed by analyzing the data obtained in the 1st and 2nd National Acid Deposition Survey by Japan Environmental Laboratories Association. In western Tohoku (WT) and Hokuriku (HR) areas in AASJ, in spite of large amounts of precipitation in winter, concentrations of non sea salt (nss-)SO₄ ^2? are not as low as the other areas, and nss-Ca²⁺ in these areas is lower than the other areas. As a result, H⁺ concentrations of precipitation in these areas are somewhat higher than other areas. From the temporal analysis of daily sampled data and back trajectory analysis of air mass, it was found that the concentrations of nss-SO₄ ^2?, NO₃ ^?, NH₄ ⁺ and nss-Ca²⁺ are correlatively varied when air mass come from the Asian Continent, showing higher concentrations at the western sites in AASJ and depending on the meteorological conditions such as the direction of in flow air mass.     

Geochemical Distribution of Selected Heavy Metals in Stream Sediments Affected by Tannery Activities

Bayesian regularized back-propagation neural network (BRBPNN) was developed for trend analysis, acidity and chemical composition of precipitation in North Carolina using precipitation chemistry data in NADP. This study included two BRBPNN application problems: (i) the relationship between precipitation acidity (pH) and other ions (NH₄ ⁺, NO₃ ^?, SO₄ ^2?, Ca²⁺, Mg²⁺, K⁺, Cl^? and Na⁺) was performed by BRBPNN and the achieved optimal network structure was 8-15-1. Then the relative importance index, obtained through the sum of square weights between each input neuron and the hidden layer of BRBPNN(8-15-1), indicated that the ions' contribution to the acidity declined in the order of NH₄ ⁺ > SO₄ ^2? > NO₃ ^?; and (ii) investigations were also carried out using BRBPNN with respect to temporal variation of monthly mean NH₄ ⁺, SO₄ ^2? and NO₃ ^? concentrations and their optimal architectures for the 1990–2003 data were 4-6-1, 4-6-1 and 4-4-1, respectively. All the estimated results of the optimal BRBPNNs showed that the relationship between the acidity and other ions or that between NH₄ ⁺, SO₄ ^2?, NO₃ ^? concentrations with regard to precipitation amount and time variable was obviously nonlinear, since in contrast to multiple linear regression (MLR), BRBPNN was clearly better with less error in prediction and of higher correlation coefficients. Meanwhile, results also exhibited that BRBPNN was of automated regularization parameter selection capability and may ensure the excellent fitting and robustness. Thus, this study laid the foundation for the application of BRBPNN in the analysis of acid precipitation.     

Ten years of precipitation chemistry in Haifa,Israel

Rain event samples have been collected in Haifa, Israel, for nine hydrological years 1981 to 1990. Precipitation amount, pH, SO₄ ⁼, NO₃ ^?, Cl^?, NH₄ ⁺, Na⁺, K⁺, Ca⁺⁺, Mg⁺⁺ and alkalinity of rainwater samples were recorded. The sampling and analysis program was based on WMO recommendations for background networks. The sampling was performed manually, and the analysis was based on wet chemistry for ions and atomic absorptions for metals. Data of 187 rain samples showed that the average pH was 5.3±1.1∶ 26% of the rain events were below pH of 5.6 and 23% above pH of 7.0. Some simple chemical mass-balance considerations indicate that natural sources, sea salt and soil carbonates are the main contributors to rain chemistry. However, the presence of low pH events observed over the years suggests that the impact of anthropogenic emissions may overwhelm the buffering capacity of the alkaline aerosol.     

Chemical and Statistical Analysis of Precipitation in Singapore

The results of chemical analyses of precipitation samples collected in Singapore between August 1997 and July 1998 are presented. Major inorganic and organic ions were determined in 169 rain samples collected using an automated wet-only sampler. The daily sample pH values ranged from 3.49 to 6.54 with a volume-weighted mean of 4.50, and about 88% of the samples had pH values less than 5.0 Nss-SO₄ ^2? accounted for about 53 % of the sum of anions in rain, whereas chloride, nitrate, formate, and acetate accounted for the remainder. Rain chemistry data were analyzed using principal component analysis to find possible sources of the measured chemical species. Three components that accounted for 83.5% of the total variance were extracted: sea-spray (Na⁺, Cl^? and and Mg²⁺) and soil particles (Ca²⁺ and K⁺), acid factor (nss-SO₄ ^2?, NO₃ ^?, NH₄ ⁺, and H⁺), and biomass burning (HCOO^? and CH₃COOO^?).     

An analysis of spatial variability of the dominant ions in precipitation in the eastern United States

Data of the Multistate Atmospheric Power Production Pollution Study (MAP3S) and the National Atmospheric Deposition Program (NADP) were utilized to develop wet deposition spatial distribution patterns for the eastern United States for 1979. The ions of SO₄ ^?, NO₃ ^?, H⁺, and NH₄ ⁺ were selected for study since they are the most prominent ones found in precipitation. Total wet deposition for 1979 was normalized to one centimeter of precipitation and objectively analyzed using the Synagraphic Mapping System (SYMAP) technique. Gradients of SO₄ ^? and NO₃ ^? were found to be essentially uniform, both to the east and west of the major pollution regions. An increased gradient in normalized deposition for SO₄ ^?, NO₃ ^?, and H⁺ was found in the Appalachian Mountain region. Estimates of total wet deposition were obtained by using the normalized deposition values in conjunction with precipitation as reported by the National Climatic Center. SYMAP analyses of the estimated total wet deposition were localized in nature due to precipitation variations between sites.     

Niederschlags-Chemismus und atmosphärische Element-Deposition in einem an der Nordseeküste von Schleswig-Holstein gelegenen Agrarökosystem

Precipitation chemistry and atmospheric element-deposition in an agroecosystem at the North-Sea Coast of Schleswig-Holstein The objective of this study was to examine the chemistry of bulk precipitation and atmospheric element inputs in an arable soil near the North Sea coast of Schleswig-Holstein, North Germany. Bulk precipitation was collected at weekly intervals from November 1989 to October 1991. Precipitation amount, pH, electrical conductivity, and concentrations of Na⁺, K⁺, NH₄⁺, Mg²⁺, Ca²⁺, Cl^?, NO₃^?, and SO₄^2? were recorded. The average volume-weighted pH was 5.5 and the average EC was 92 μS cm^?1. Sodium and Cl^? were with 64% and 76% the dominant ions (equivalent concentration) in bulk precipitation indicating the influence of the North Sea. The contribution of marine alkalinity to neutralization reactions of bulk precipitation was negligible (1%). The neutralizing substances NH₃ (63%) and Carbonate (36%) were more important. Deposition rates were in 1990 and 1991 97.0 and 51.7 kg Na⁺ ha^?1, 6.2 and 4.0 kg K⁺ ha^?1, 15.0 and 8.4 kg Mg²⁺ ha^?1, 13.2 and 10.4 kg Ca²⁺ ha^?1, 12.3 and 9.5 kg NH₄⁺-N ha^?1, 8.0 and 5.9 kg NO₃^?-N ha^?1, 168 and 83.1 kg Cl^? ha^?1 and 19.1 and 12.7 kg SO₄^2?-S ha^?1. In 1990 both more westerly winds and stronger wind-forces occurred than in 1991 and resulted in higher inputs of marine origin. Calculated on Cl^? basis 93% of Na⁺, 55% of K⁺, 74% of Mg²⁺, 24% of Ca²⁺, and 36% of SO₄^2? were of marine origin. Atmospheric input of marine origin supplied 39–72% of Mg and 21–37% of S requirement for crop production. The North Sea is an important source providing significant amounts of these elements to agricultural crops.     

Morphology and Solutes Content of Atmospheric Particles in an Urban and a Natural Area of São Paulo State, Brazil

The objectives of this work were to characterize and compare the chemical composition of the water-soluble fraction of the PM₁₀ particles (Dp < 10μm) in two sites: one inside the Metropolitan Area of São Paulo (MASP) and another, 250km apart, inside the State Park of Serra do Mar (CUNHA) part of the Atlantic Forest Reserve, both located in São Paulo State, Brazil. The atmospheric particles were collected during dry and wet season. The morphologic parameters of the particles were characterized for the different size fractions of the collected material. In the aqueous extract of the particulate fine fraction the major ions (Na⁺, K⁺, Mg²⁺, Ca²⁺, Cl^?, NO₃ ^?, NH₄ ⁺, SO₄ ^2?) and trace elements (Al, Mn, Fe, Pb, Cd, Zn, Ti, Ni, Cu, Co, Ba) were determined. The morphological characteristics of the particles collected within the MASP are typical of polluted environment while in CUNHA there is no evidence of this type of contribution. Regarding the solute concentrations it was observed that the most abundant major ions and trace elements were K⁺, Ca²⁺, Na⁺, Cl^? and Pb, for CUNHA and NO₃ ^?, SO₄ ^2?, NH₄ ⁺ and Mn, Ni, Pb, Co, Cd and Ba for MASP. These differences are associated with the different sources of the particles. In the urban area they are predominantly of pollution origin, mainly from vehicle emissions, and road dust suspension, while in the State Park they are mainly of biogenic, terrigenous and oceanic origins. For these reasons the CUNHA region can be considered to be a regional reference site for studies concerning eventual disturbances in the Cunha background site, derived from transported pollution.     

Trends of Major Inorganic Species at the Small Watershed Ecosystem in Northern Tama Hills, the Western Tokyo Metropolitan Area, Japan

Acid rain impacts on the small forested watershed in northern Tama Hills in the western Tokyo metropolitan area Japan were investigated by surveying the trends of major inorganic species in rain and spring water during the years from 1991 to 1997. The ecosystem had been stressed by the annual H⁺-deposition of around 0.43 kmol/ha. The spring water outflow corresponded to ca. 27% of the precipitation. Budgets for the precipitation input and spring water output gave good balance for Cl^?,?0.01 ±0.09 kmol/ha, net gains for H⁺, NO₃ ^? and SO₄ ^2?, and to the contrary, relatively large net losses for Na⁺, Mg²⁺, Ca²⁺, Si(as H₄SiO₄) and HCO₃ ^?, thus suggesting the dissolution of chemical weathered products of silicate minerals. Further, in spring water, some concentration relationships were found: CNa⁺ = 376.5?2.05CCl^? (R²=0.748), CNa⁺=12.69+0.5556CHCO₃ ^? (R²=0.872) and CH₄SiO₄=130.0 + 1.108CHCO₃ ^? (R²=0.816). Evidently, the spring water chemistry reflected probable geochemical changes in the soil layer of the watershed. Mass balance in the ecosystem and estimation of the spring water output of chemical weathered products were investigated     

Fog- and Rainwater Chemistry in the Tropical Seasonal Rain Forest of Xishuangbanna, Southwest China

Fogwater, fog drip and rainwater chemistry were examined at a tropical seasonal rain forest in Xishuangbanna, southwest China between November 2001 and October 2002. During the period of observation, 204 days with the occurrence of radiation fog were observed and the total duration of fog was 1949 h, of which 1618 h occurred in the dry season (November to April), accounting for 37.0% of the time during the season. The mean pH of fogwater, fog drip and rainwater were 6.78, 7.30, and 6.13, respectively. The ion with the highest concentration for fog- and rainwater was HCO₃ ^?, which amounted to 85.2 and 37.3 μeq l^?1, followed by Ca²⁺, Mg²⁺ and NH₄ ⁺. Concentrations of NO₃ ^?, HCO₃ ^?, NH₄ ⁺, Ca²⁺, and K⁺ in fogwater samples collected in the dry season were significantly greater when compared to those collected in the rainy season. It was found that the ionic concentrations in fog drip were higher than those in fogwater, except for NH₄ ⁺ and H⁺, which was attributed to the washout of the soil- and ash-oriented ions deposited on the leaves and the alkaline ionic emissions by the leaves, since biomass burns are very common in the region and nearby road was widening.     

Precipitation Composition in the Ohio River Valley: Spatial Variability and Temporal Trends

Sulfate (SO₄ ^2?), nitrate (NO₃ ^?) and ammonium (NH₄ ⁺) concentrations in precipitation as measured at NADP sites within the Ohio River Valley of the Midwestern USA between 1985 and 2002 are quantified and temporal trends attributed to changes/ variations in (i) the precipitation regime, (ii) emission patterns and (iii) air mass trajectories. The results indicate that mean SO₄ ^2? concentrations in precipitation declined by 37–43% between 1985 and 2002, while NO₃ ^? concentrations decreased by 1–32%, and NH₄ ⁺ concentrations exhibited declining concentrations at some sites and increasing concentrations at others. The change in SO₄ ^2? concentrations is in broad agreement with estimated reductions in sulfur dioxide emissions. Changes in NO₃ ^? concentrations appear to be less closely related to variations in emissions of oxides of nitrogen and exhibit a stronger dependence on weekly precipitation volume. Up to one quarter of the variability in log-transformed weekly NO₃ ^? concentrations in precipitation is explicable by variations in precipitation volume. Trends in annual average log-transformed SO₄ ^2? concentrations exhibit only a relatively small influence of variability in weekly precipitation amount but at each of the sites considered the variance explanation of annual average log-transformed SO₄ ^2? by sampling year was increased by removing the influence of precipitation volume. Annual mean log-transformed ion concentrations detrended for precipitation volume (by week) and emission changes (by year) exhibit positive correlations at all sites, indicating that the residual variability of SO₄ ^2?, NO₃ ^? and NH₄ ⁺ may have a common source which is postulated to be linked to synoptic scale variability and air mass trajectories.     

Interactive Effects of Nitrogen Source and Salinity on Growth Indices and Ion Content of Indian Mustard

ABSTRACT

The interactions between salinity and different nitrogen (N) sources nitrate (NO₃ ^?), ammonium (NH₄ ⁺), and NO₃ ^? + NH₄ ⁺ were investigated on Indian mustard (Brassica juncea cv. RH30). Treatments were added to observe the combined effect of two salinity levels (8 and 12 ds m^{? 1}) and three nitrogen sources (NO₃ ^?, NH₄ ⁺, and NO₃ ^? + NH₄ ⁺) on different growth parameters and mineral composition in different plant parts, i.e., leaves, stem, and root. Salinity has been known to affect the uptake and assimilation of various essential nutrients required for normal growth and development. Different growth parameters, i.e., leaf area, dry weight of different plant parts, absolute growth rate (AGR), relative growth rate (RGR), and net assimilation rate (NAR) declined markedly by salinity at pre-flowering and flowering stages. All growth indices were less sensitive to salinity (12 d s m^{? 1}) with the nitrate form of nitrogen. It is pertinent mention that a high dose (120 kg ha^{? 1}) of nitrogen in ammonium form NH₄ ⁺, acted synergistically with salinity in inhibiting growth. Plants fed with combined nitrogen (NO₃ ^? + NH₄ ⁺) had an edge over individual forms in ameliorating the adverse effects of salinity on growth and yield. Under salt stress, different nutrient elements such as N, phosphorus (P), potassium (K⁺), and magnesium (Mg^{2 +}) were decreased in different plant parts (leaves, stem, and root). The maximum and minimum reduction was observed with ammoniacal and combined form of nitrogen, respectively, while the reverse was true of calcium (Ca^{2 +}), sodium (Na⁺), chloride (Cl^?), and sulfate (SO₄ ^2?) at harvest. Nitrogen application (120 Kg ha^{? 1}) in combined form had been found to maintain highest concentrations of N, P, Mg^{2 +}, and Ca^{2 +} along with reduced concentrations of Na⁺, Cl^?, and SO₄ ^{2 ?}. However, reverse was true with ammoniacal form of nitrogen.     

Does the potential ammonium fixation of soils have an impact on the optimum nitrogen fertilizer rate?

Field experiments were conducted to determine the effect of nitrogen (N) fertilizer forms and doses on wheat (Triticum aestivum L.) on three soils differing in their ammonium (NH₄) fixation capacity [high = 161 mg fixed NH₄-N kg^?1 soil, medium = 31.5 mg fixed NH₄-N kg^?1 soil and no = nearly no fixed NH₄-N kg^?1 soil]. On high NH₄⁺ fixing soil, 80 kg N ha^?1 Urea+ ammonium nitrate [NH₄NO₃] or 240 kg N ha^?1 ammonium sulfate [(NH₄)₂SO₄]+(NH₄)₂SO₄, was required to obtain the maximum yield. Urea + NH₄NO₃ generally showed the highest significance in respect to the agronomic efficiency of N fertilizers. In the non NH₄⁺ fixing soil, 80 kg N ha^?1 urea+NH₄NO₃ was enough to obtain high grain yield. The agronomic efficiency of N fertilizers was generally higher in the non NH₄⁺ fixing soil than in the others. Grain protein was highly affected by NH₄⁺ fixation capacities and N doses. Harvest index was affected by the NH₄⁺ fixation capacity at the 1% significance level.     

Ion Fluxes with Bulk and Throughfall Deposition along an Urban–Suburban–Rural Gradient

Fluxes of principal anions and cations with bulk and throughfall deposition during the growing period (April–September) were investigated for three years (2001–2003) at three sites differently exposed to the second biggest Lithuanian city – Kaunas. Fluxes of all investigated anions (SO₄ ^2?, NO₃ ^? and Cl^?) and most cations were found to be the highest in suburban area to compare with both – Rural and urban sites. The highest seasonal variability of monthly ion fluxes and the highest differences between throughfall and bulk fluxes (net throughfall) were recorded in suburban area. The highest throughfall enrichment by sulphur was detected in spring and the beginning of summer (April, May) in urban and especially in suburban sites. For nitrogen compounds (NO₃ ^?, NH₄ ⁺) positive net throughfall values were characteristic for urban and suburban sites and negative for rural site almost during the entire growing period. Uptake of NH₄ ⁺ ions was detected to be much higher of that for nitrates in rural area (46% vs. 22%). The most intensive enrichment of throughfall fluxes by K⁺ ions took place during the summer time (May, June, July), however, intensity of potassium leaching at the same amount of precipitation was the highest in suburban area.     

Characteristics of ammonium and nitrate fluxes along the roots of Picea asperata

Nitrogen (N), ammonium (NH₄⁺) and nitrate (NO₃^?), is one of the key determinants for plant growth. The interaction of both ions displays a significant effect on their uptake in some species. In the current study, net fluxes of NH₄⁺ and NO₃^? along the roots of Picea asperata were determined using a Non-invasive Micro-test Technology (NMT). Besides, we examined the interaction of NH₄⁺ and NO₃^? on the fluxes of both ions, and the plasma membrane (PM) H⁺-ATPases and nitrate reductase (NR) were taken into account as well. The results demonstrated that the maximal net NH₄⁺ and NO₃^? influxes were detected at 13–15?mm and 8–10.5?mm from the root apex, respectively. Net NH₄⁺ influx was significantly stimulated with the presence of NO₃^?, whereas NH₄⁺ exhibited a markedly negative effect on NO₃^? uptake in the roots of P. asperata. Also, our results indicated that PM H⁺-ATPases and NR play a key role in the control of N uptake.     

Relationships between Acid Ions and Carbonaceous Fly-Ash Particles in Deposition at European Mountain Lakes

The concentrations of major ions and spheroidal carbonaceous fly-ash particles (SCPs) in bulk deposition were determined in weekly samples from six European mountain lakes during 1997/98. SCPs are produced only from high temperature combustion of fossil-fuels and therefore provide an unambiguous indicator of atmospheric deposition from this source. Positive correlations were observed between SCPs and SO₄ ^2?, NO₃ ^? and NH₄ ⁺ at all sites except for some determinands at Jorisee (Switzerland) and Starolesnienske (Slovakia). Correlations between SCPs and SO₄ ^2? + NO₃ ^? were always more positive than for SCPs with 'total acid ions' (SO₄ ^2? + NO₃ ^? + NH₄ ⁺). This is in agreement with the expectation that the contribution to NH₄ ⁺ deposition made by fossil-fuels is negligible. Good positive correlations between SCPs and all acid anions were observed at Estany Redo (Pyrenees); lower but still positive correlations were observed for all acid ions with SCPs at Gossenköllesee (Austria), Lochnagar and Kårvatn (central Norway), whilst little trend in correlation was observed for Jorisee and Starolesnienske. It is suggested that this gradient reflects the influence of fossil-fuels on acid deposition in these areas. A high positive correlation was observed between SCP and Cl^? at Gossenkollesee possibly as a result of HCl from coal combustion.