The phytotoxic risk of ambient air pollution to local vegetation was assessed in Selangor State, Malaysia. The AOT40 value was calculated by means of the continuously monitored daily maximum concentration and the local diurnal pattern of O3. Together with minor risks associated with the levels of NO2 and SO2, the study found that the monthly AOT40 values in these peri-urban sites were consistently over 1.0 ppm·h, which is well in exceedance of the given European critical level. Linking the O3 level to actual agricultural crop production in Selangor State also indicated that the extent of yield losses could have ranged from 1.6 to 5.0% (by weight) in 2000. Despite a number of uncertainties, the study showed a simple but useful methodological framework for phytotoxic risk assessment with a limited data set, which could contribute to appropriate policy discussion and countermeasures in countries under similar conditions. There is a large potential of phytotoxic risk on vegetation in Selangor State, Malaysia.

We intensively surveyed the concentrations of chemical species in aerosols and gases using a four-stage filter-pack method at a site in Japan facing the Sea of Japan in winter with 6-h sample intervals. A few chloride species emitted anthropogenically were detected, and the HCl (g) concentration was quite low. The number of chloride species artifacts was also low. The HNO₃ (g) concentration was significantly higher when the monitored air mass passed over the Korean Peninsula compared to when it did not pass over the Korean Peninsula. In addition, the HNO₃ (g) concentration was significantly higher when the air mass arrived at the monitoring site by passing the route at lower latitude than the latitude of the monitoring site. On the other hand, the SO₂ (g) concentration showed no change between various trajectories of the air mass. The [Formula: see text] (p)/non-seasalt- (nss-) [Formula: see text] (p) ratio was intermediate between the compositions of (NH₄)₂SO₄ and NH₄HSO₄ when the air mass passed over the Korean Peninsula, whereas it was intermediate between NH₄HSO₄ and H₂SO₄ when the air mass did not pass over the Korean Peninsula. We detected the transboundary transport of sulfur dioxide with high time-resolution monitoring at two separate monitoring points: the current monitoring site and Oki Island.

Analysis of the sensitivity of soils to acidification caused by the deposition of atmospheric pollutants has been one of the major scientific issues in Europe during the past few decades. In the present study, critical loads of acid deposition were calculated using the most accurate datasets available at present for European soils, by the “Simple Mass Balance” method. The results show that the soils most sensitive to acid deposition are Histosols, Cryosols and Podzols in cold areas in northern countries, followed by Lithic and Haplic Leptosols (Dystric) developed on acid parent materials. The highest critical loads corresponded to soils developed over calcareous rocks and soils in areas subject to high precipitation, even those dominated by poorly weatherable primary mineral. In the latter case critical alkalinity leaching is the main variable that determines the value of critical loads, because of the buffering action of the dissolution of aluminium compounds. The results were compared with those obtained by the Stockholm Environmental Institute in the same area, but with a different method of analysis. It was found that the results are highly dependent on the method used to perform the analysis.

Field study at the Cervenohorske sedlo (1,013 m a.s.l.) (Hruby Jesenik Mountains, the Czech Republic, Central Europe) during 1999-2002 has been conducted in order to analyse the chemistry of rain/snow water using bulk and throughfall collector and fog/cloud water using modified passive Grunow collector. Fog water input to coniferous forest (Picea abies) was quantified using canopy balance method. For all samples pH, and the concentrations of [graphic removed] , Ca²⁺, K⁺, Mg²⁺, Na⁺, Cl-, [graphic removed] , and [graphic removed] were measured. The volume-weighted mean pH value varied from 4.92 to 5.43 in open bulk precipitation, from 4.30 to 4.71 in throughfall and from 4.66 to 5.23 in fog water. The fog droplets generally contain higher ion concentrations than rainwater. The related enrichment factors lie between 1.1 and 10.7 for the relevant species. The fog samples exhibit higher concentrations of [graphic removed] and [graphic removed] as compared to the bulk samples during 2000-2002. [graphic removed] are 5.7-10.7 times more concentrated in fog water and [graphic removed] are 3.4-7.2 times more concentrated in fog water. These differences may result from the height and characteristics of formation of the droplets. Based on canopy balance method, the annual fog water inputs were estimated to be 22 and 19% of rain and snow annual amounts in 1999 and 2000, respectively. For [graphic removed] , [graphic removed] , and [graphic removed] , the contribution of fog deposition in total (bulk + fog) deposition is estimated as 54, 47, and 42%, respectively.

In the study area physical and chemical factors control the composition of surface and groundwaters, which in turn determine the water quality of the “Biviere di Gela” lake. These factors combine to create diverse water types which change their compositional character spatially as rainfall infiltrates the soil zone, moves down a topographically defined flow path, and interacts with bedrock minerals. Low-salinity waters, which represent the initial stage of underground circulation, start dissolving calcium carbonate from the local rocks. The progressive increase in salinity, characterized by substantially higher Ca, SO₄, Na and Cl concentrations, suggests that dissolution of CaSO₄ and NaCl is an important process during water-rock interactions. The “Biviere di Gela” lake is often separated into two units (Lago Grande and Lago Piccolo). “Lago Grande” water is generally of Na-SO₄-Cl-type, whereas “Lago Piccolo” water is of Na-Cl-SO₄-type. Their total content of dissolved salts varies with season, the amount of rainfall, and inflow of ground and drainage water. Over time, an increasing trend towards greater salinity and also sudden changes in the relative abundances of Cl and SO₄ have been recorded for the “Lago Grande.” The isotope composition of the lake water appears to be affected by inflow of ground and surface waters and also by evaporative loss. The nitrate content of waters from the recharge basin is of particular concern because it contributes to lake eutrophication. The trace element contents do not evidence the presence of any significant metal contamination of lake waters, although a future potential hazard of metals bioaccumulation by the aquatic biota must be taken into consideration. Finally, a water balance for the basin shows that a drop in precipitation of about 20% might be critical for lake survival.

Temporal trends of non-sea salt (nss-) sulfate and nitrate were analyzed from nationwide precipitation chemistry measurements provided by the Ministry of the Environment (MOE) for the 1988-2002 fiscal years (April-March). The concentrations and deposition of nss-sulfate were found to be decreasing, and those of nitrate were stable or slightly increasing at most sites. These deposition trends were discussed from the viewpoint of emissions of SO₂ and NOX during the period of interest. Because monitoring techniques have changed in the number of active sites, samplers, and analytical methods during the operation period, the median of all annual depositions measured in Japan in a specific year was selected as the annual representative. The contribution of specific emission sources was also calculated for 1990 on the basis of the nss-sulfate and nitrate deposition in Japan obtained with a model simulation in which the model did not include volcanic emissions from Mt. Oyama, Miyakejima Island, which began to erupt suddenly and violently in 2000. For nss-sulfate, the calculated deposition agrees well with the intensity and trends of the median up to 1999. After 2000, a higher deposition than calculated in the preceding years was evident, which is attributable to the volcanic SO₂ from Mt. Oyama. For nitrate, both the calculated and observed depositions were slightly increasing; however, the calculation was found to exceed the observation.

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.

This study examines the seasonal variability in levels of nitrogen (N) leaching and acidity in four acid impacted upland regions of the UK: the South Pennines, Snowdonia, Galloway and the Mourne Mountains. All regions are acidified, with median pH values of <5.5. The South Pennines exhibit excess sulphate concentrations an order of magnitude higher than those for other regions and have the lowest pH values of all the regions. Nitrate concentrations are highest in the South Pennines (seasonal medians 20-26 μeq l-¹) and the Mourne Mountains (seasonal medians 9-26 μeq l-¹). Surface water in the Mourne Mountains is the most highly N impacted in terms of the proportional contribution of N to acidity. All N species exhibit seasonality, with greater retention by catchment soils and vegetation in August. This seasonality is most marked in Snowdonia and least marked in the South Pennines. This implies that the South Pennines have reached an advanced stage of N saturation. Despite the reductions in S deposition, xSO₄ is the dominant anion for all sites in the South Pennine and Snowdonia regions. A strong negative relationship between the contribution of NO₃ to total acidity and DON was observed for all regions except the South Pennines. It is hypothesized that catchments dominated by organic rich soils produced more DON and have an increased capacity to immobilise NO₃. Seasonal nitrogen budgets show that over 60% of the N inputs are retained within catchments, and no site retains all incoming N throughout the year.

Two identical experimental subsurface-flow constructed wetlands were operated at relatively high organic loading rates (23 g COD m-² day-¹) for 4 months to evaluate their relative ability to remove either dissolved organic carbon (glucose, considered to be a readily biodegradable substrate) or particulate organic carbon (starch, considered to be a slowly biodegradable substrate). The systems were built using plastic containers (0.93 m long, 0.59 m wide and 0.52 m high) that were filled with an 0.35 m layer of wetted gravel (D₆₀ = 3.5 mm, uniformity coefficient Cu = D₆₀/D₁₀ = 1.7) and the water level was maintained at 0.05 m under the gravel surface to give a water depth of 0.30 m. The results indicated that there was no significant difference in COD removal between the two systems. Both systems generally had COD removal rates of over 90%, which is quite high if the heavy load applied is taken into account. The removal of ammonium was greater in the glucose-fed system (57%) in comparison with the starch-fed system (43%). Based on mass balance calculations and stoichiometric relationships, it was estimated that denitrification and sulphate reduction were minor pathways for the removal of organic matter. Indirect observations allowed to assume that methanogenesis made a highly significant contribution to the removal of organic matter.

Background, Aim and Scope Acid deposition has become a concern in south China in recent years. This phenomenon has increased to a dramatic extent with the large use of cars and coal- fueled power plants. As a consequence, soils are becoming acidified and their element dynamics will change. A decrease in the nutrient availability will lead to slower plant growth and maybe to a change in the forest type with current species being replaced by new ones with less nutrient requirements. Because of these reasons, it is important to understand how the dynamics of elements will change and what mechanism is part of the process. This knowledge is important for modeling the acidification process and either finding ways to counter it or to predict its consequences. The primary purpose of this study was to provide information about how the dynamics of K, Na, Ca, Mg and P are affected by acid deposition in a typical forest in southern China. Materials and Methods: Experimental soils and saplings were collected directly from the monsoon evergreen broad-leaved forest in Dinghushan. All saplings were transplanted individually into ceramic pots in August 2000 and placed in an open area near their origin site. Pot soils were treated weekly from October, 2000 to July, 2002 with an acidic solution at pH 3.05, pH 3.52, pH 4.00 or pH 4.40, or with tap water as a control. The concentrations of SO42-, NO3-, K+, Na+, Ca2+, Mg2+ and available P and the pH were measured in soil and leachate samples taken at different times. The sapling leaves were collected and their element concentrations were measured at the end of the experiment. Results: Concentrations of soil exchangeable Ca and Mg decreased quickly over time, although only Ca showed changes with the acidic solution treatment and soil exchangeable K was stable because of soil weathering. Leaching of K, Mg and Ca was dependent upon the treatment acidity. Soil available P decreased slowly without any correlation with the acidity of the treatment. All the NO3- added by the treatment was taken up by the plants, but the SO42- added accumulated in the soil. Discussion: Amongst the plant species, Schima superba was little affected by the treatment, the leaf P content was affected in Acmena acuminatissima plants and Cryptocarya concinna was the most susceptible species to soil acidification, with a marked decrease of the leaf K, Ca and Mg concentrations when the treatment acidity increased. Conclusions: Simulated acid deposition affected the dynamics of K, Ca and Mg in the monsoon evergreen broad-leaved forest. The dynamics of Ca in the soil and of K, Mg and Ca in the soil leachates were affected by the acidic solution treatment. If such a soil acidification occurs, Cryptocarya concinna will be amongst the first affected species, but Schima superba will be able to sustain a good growth and mineral nutrition. Recommendations and Perspectives: Acid deposition will lead to imbalance the nutrient elements in the evergreen broad-leaved forest because of accelerated leaching losses of soil exchangeable Ca and Mg. Measures should be developed to slow down soil acidification or nutrient decrease.