Biogeochemistry of aluminum in a forest catchment in the Czech Republic impacted by atmospheric inputs of strong acids

The Lysina catchment in the Czech Republic was studied to investigate the biogeochemical response of Al to high loadings of acidic deposition. The catchment supports Norway spruce plantations and is underlain by granite and podzolic soil. Atmospheric deposition to the site was characterized by high H⁺ and SO₄ ^2– fluxes in throughfall. The volume-weighted average concentration of total Al (Al_t) was 28 mol L^–1 in the O horizon soil solution. About 50% of Al_t in the O horizon was in the form of potentially-toxic inorganic monomeric Al (Al_i). In the E horizon, Al_t increased to 71 mol L^–1, and Al_i comprised 80% of Al_t. The concentration of Al_t (120 mol L^–1) and the fraction of Al_i (85%) increased in the lower mineral soil due to increases in Al_i and decreases in organic monomeric Al (Al_o). Shallow ground water was less acidic and had lower Al_t concentration (29 mol L^–1). The volume-weighted average concentration of Al_t was extremely high in stream water (60 mol L^–1) with Al_i accounting for about 60% of Al_t. The major species of Al_i in stream water were fluorocomplexes (Al-F) and aquo Al³⁺. Soil solutions in the root zone were undersaturated with respect to all Al-bearing mineral phases. However, stream water exhibited Al_i concentrations close to solubility with jurbanite. Acidic waters and elevated Al concentrations reflected the limited supply of basic cations on the soil exchange complex and slow weathering, which was unable to neutralize atmospheric inputs of strong acids.     

The relationship between salmonid fish densities and critical ANC at exceeded and non-exceeded stream sites in Scotland

The critical load concept is now accepted throughout Europe as a means of estimating the sensitivity of key components of aquatic and terrestrial ecosystems to atmospheric inputs of sulphur (S) and nitrogen (N). Current UK freshwater maps, based on steady-state water chemistry, are derived using a critical acid neutralising capacity (ANC_LIM) value of zero eql^–1, which is based on the probability of occurrence of salmonid fish in lakes. In practice most acidification damage to salmonid fish occurs in nursery streams at the emergence and first feeding stages. In general a clear relationship exists between salmon (Salmo salar L.) and trout (S. trutta L.) densities in Scottish streams and ANC values. However, differences between sites depend on which ANC value is used (eg maximum, minimum or mean). By contrast, when the exceedance of critical loads is compared with salmonid densities the relationship is less clear because many exceeded sites have good salmonid densities. Many of these latter sites are found in north-west Scotland where sea-salt inputs are high and ANC is usually greater than zero eql^–1, although diatom-based studies indicated slight acidification of these waters, with a point of change in diatom flora close to ANC=20 eql^–1. These false exceedances are probably due to preferential adsorption of acidic SO₄ deposition which results in an overestimate of exceedance values. All sites with a mean ANC 0 are fishless but some sites with negative minimum ANC values had normal salmonid densities. Consequently a mean ANC_LIM value of zero in the critical load equations for UK freshwaters appears to be too low to protect salmonid stocks. Values between 20–50 eql^–1 represent a more realistic range if prevention of long term damage to salmonid stocks is to be achieved.     

Acidic deposition,ecosystem processes,and nitrogen saturation in a high elevation Southern Appalachian watershed

High-elevation red spruce-Fraser fir forests in the Southern Appalachian mountains: 1) receive among the highest rates of atmospheric deposition measured in North America, 2) contain old-growth forests, 3) have shown declines in forest health, 4) have sustained high insect-caused fir mortality, and 5) contain poorly buffered soils and stream systems. High rates of nitrogen and sulphur deposition (1900 and 2200 Eq·ha^–1·yr^–1, respectively) are dominated by dry and cloud deposition processes. Large leaching fluxes of nitrate-nitrogen (100–1400 Eq·ha^–1·yr^–1) occur within the soil profile. We have expanded the study to the watershed scale with monitoring of: precipitation, throughfall, stream hydrology, and stream chemistry. Two streamlets drain the 17.4 ha Noland Divide Watershed (1676–1920m) located in the Great Smoky Mountains National Park. A network of 50 20x20 m plots is being used to assess stand structure, biomass, and soil nutrient pools. Nitrate is the predominant anion in the streamlets (weighted concentrations: 47 and 54 eq·L^–1 NO₃ ^–; 31 and 43 eq·L^–1 SO₄ ^2–). Watershed nitrate export is extremely high (1000 Eq·ha^–1 yr^–1), facilitating significant base cation exports. Stream acid neutralizing capacity values are extremely low (–10 to 20 eq·L^–1) and episodic acidifications (pH declines of a full unit in days or weeks time) occur. Annual streamwater sulfate export is on the order of 770 Eq·ha^–1yr^–1 or about one-third of total annual inputs, indicating there is net watershed sulfate retention. The system is highly nitrogen saturated (Stage 2, Stoddard, 1994) and this condition promotes both chronic and episodic stream acidification.     

Bioaccumulation of selenium by floating aquatic plants

The degree to which floating aquatic plants concentrate Se in tissues was determined for four species grown in solutions containing various levels of Se. Results of this greenhouse study showed that all four plant species, Azolla caroliniana, Eichhornia crassipes, Salvinia rotundi folia, and Lemna minor absorbed Se quickly upon exposure to Se in water as concentrated as 2.5 g Se mL^–1, and attained maximum tissue concentrations within 1 to 2 weeks. Azolla absorbed Se to the highest tissue concentration (about 1000 g Se g^–1 dry matter) from the 2.5 g Se mL^–1 solution, followed by Salvinia (700 g Se g^–1), Lemna (500 g Se g^–1),and Eichhornia (300 g Se g^–1). Plant growth appeared unaffected by solution Se concentrations lower than about 1.25 g mL^–1. These results indicate potential for rapid Se movement from water into aquatic food chains, and for use of aquatic plants for Se removal in wastewater treatment systems.     

Surface ozone concentrations and exposures during growing season at the Lithuanian rural site

The surface ozone (O₃) data show an increase by 2.6 % per year during the period 1982–1994 at the rural site of Lithuania. WHO (World Health Organization), UN-ECE (United Nations Economic Commission for Europe), CES (Commission of the European Communities) guideline values for the protection of vegetation from adverse effects are exceeded during the growing season at the Preila coastal station. Ozone exposures for different concentration threshold are estimated during daylight hours in April-September. These values above 60 g/m³ varied between 10 000 and 43 000 (g/m³) ·h, above 80 g/m³ — between 1700 and 15 000 (g/m³) ·h, above 100 g/m³ — between 130 and 3700 (g/m³) ·h during separate years. Maximum hourly ozone values were observed from 116 to 228 g/m³ during this period.     

Ionic composition of rainwater and atmospheric aerosols in Sardinia,southern Mediterranean

The ionic composition of 55 aerosol samples and 31 precipitation events collected in a coastal site in southern Sardinia (Capo Carbonara, 39°06 N; 09°31 E) were compared. The samples were collected during one year period (Oct'90/Oct'91) and showed high variability in composition according to meteorological conditions. Rain and soluble part of aerosol showed a strikingly similar ionic composition: most significant anions were chlorine and sulphate, and sodium is the principal cations, followed by magnesium and calcium. The acid events are associated with N-NW trajectories (anthropogenic influxes from N. Europe) with avg. pH=4.65, non sea salt (nss) Ca=60 eq/l and NO₃/_nssSO₄=0.6. Southern precipitations are influenced by Saharan dust alkaline effects, with avg. pH=6.75,_nssCa=271 eq/l and NO₃/_nssSO₄=0.4. Na/Cl ratio in rain is similar to sea water (0.87), whilst in aerosols there is a Cl loss (Na/Cl=1.10), probably due to reaction with nitric acid. Total fluxes of Ca, Mg, NO₃ and SO₄ were 104, 9, 64 and 113 g/cm², and wet deposition exceeded (65–90%) dry deposition. Scavenging ratios (SR) as defined by the equation:SR=[(Ci)rain/(Ci)air] ^*d, (d=1200g/m³) were calculated, using geometric means (Ci) of precipitation and aerosols collected concurrently during the period (a total of 23 samples). The SR values are Ca=3400, Cl=2400, Na, K, SO₄=1700, Mg=1000 and NO₃=750. These numbers could be useful to infer total fluxes by using simply rainwater ionic composition in Mediterranean semi-arid sites like Sardinia.     

Long-term trends in the chemistry of precipitation and lake water in the Adirondack Region of New York,USA

Long-term changes in the chemistry of precipitation (1978–94) and 16 lakes (1982–94) were investigated in the Adirondack region of New York, USA. Time-series analysis showed that concentrations of SO₄ ^2–, NO₃ ^–, NH₄ ⁺ and basic cations have decreased in precipitation, resulting in increases in pH. A relatively uniform rate of decline in SO₄ ^2– concentrations in lakes across the region (1.81±0.35 eq L^–1 yr^–1) suggests that this change was due to decreases in atmospheric deposition. The decrease in lake SO₄ ^2– was considerably less than the rate of decline anticipated from atmospheric deposition. This discrepancy may be due to release of previously deposited SO₄ ^2– from soil, thereby delaying the recovery of lake water acidity. Despite the marked declines in concentrations of SO₄ ^2– in Adirondack lakes, there has been no systematic increase in pH and ANC. The decline in SO₄ ^2– has corresponded with a near stoichiometric decrease in concentrations of basic cations in low ANC lakes. A pattern of increasing NO₃ ^– concentrations that was evident in lakes across the region during the 1980's has been followed by a period of lower concentrations. Currently there are no significant trends in NO₃ ^– concentrations in Adirondack lakes.     

Sulphur isotope characteristics of two north Bohemian forest catchments

Sulphate concentrations and ³⁴S ratios were monitored in bulk precipitation, spruce throughfall, and soil water (depth of 30 and 90 cm) at ervená jáma (CER) and Naetín (NAC), two severely polluted sites in the Czech Republic, between December 1992 and September 1994. Throughfall [SO₄ ^2–], up to 80 mg L^–1 in winter and as low as 7 mg L^–1 in summer, was higher than [SO₄ ^2–] in bulk precipitation (annual average 6 mg L^–1). There was a distinct seasonaity in S isotope abundances, with lower ³⁴S_BULK in summer (+4 per mil CER, + 6 per mil NAC) and lower ³⁴S_TF in winter (+3 per mil CER, +4 per mil NAC). Wintertime ³⁴S_BULK was around +8 per mil at CER and +10 per mil at NAC, summertime ³⁴S_TF was close to +7 per mil at both sites. For only a 1- month period in spring, bulk precipitation S became isotopically lighter than throughfall S. Bulk precipitation data from CER were in good agreement with those from the nearby monitoring station Lesná (LES), typically differing by less than 10 mg L^–1 and 2 per mil in [SO₄ ^2–] and ³⁴S, respectively. Suction lysimeters (soil depth of 30 and 90 cm) yielded higher sulphate concentrations and lower ³⁴S ratios compared to both bulk and throughfall precipitation. Little seasonality was observed in [SO₄ ^2–] at 30 cm (around 40 mg L^–1); at 90 cm [SO₄ ^2–] was higher in winter (70 mg L^–1) than in summer (45 mg L^–1). ³⁴S at 90 cm was <+5 per=" mil=" in=" 1993=" and=" up=" to=" +7.5=" in=" 1994,=" lower=" in=" the=" first=" year=" and=" higher=" in=" the=" second=" year=" compared=" to=" the=" depth=" of=" 30=" cm.=" sulphur=" fluxes=" at=" cer=" and=" nac=" are=" characterized=" by=" distinct=" isotope=" compositions=" and=" can=" therefore=" be=" used=" to=" trace=" s=" pathways=" and=" transformations=" in=" the=" forest=">     

Measurements of atmospheric particulate carbon in Lithuania

During 1985–1989 particulate carbon concentrations were determined at suburban and rural sites in Lithuania. The main part of the continuous measurements was conducted at Preila background station (Curonian spit). Daily samples of airborne particulate matter were collected on glass fiber filters or by impactors and analysed for total carbon (TC), benzene extractable organic carbon (BEOC) and elemental carbon (EC) using combustion and optical techniques. Monthly median concentrations of total particulate carbon varied in the range 2–22 g/m³ during the period of measurements. For all the forms of particulate carbon the strong seasonal dependence was observed. The very regular seasonal cycle is characteristic for the ratio EC/TC: 0.10–0.15 and 0.30–0.35 for warm and cold periods respectively. Size distribution measurements shows that the main part of TC is in the sub-micron particle fraction — about 80–90 % in summer and even 92–98 % in winter. The concentrations of TC in size fraction <1.2>m have sharp winter peaks and summer minima. Very low concentrations and summer maxima for TC in the fraction >3.5 m have been observed. The concentrations of EC in precipitation varied from 0.02 to 0.7 mg/l and average wet deposition flux of EC was 5–7 and maximum 15–20 mg/m² per month.     

Precipitation chemistry at sinhagad-a hill station in India

The chemistry of precipitation in remote sites such as mountain tops is of interest in the study of atmospheric pollution and acid rain. The chemical composition measured at mountain site which is away from industrial and urban areas is useful as a reference level and it allows to determine the extent of anthropogenic contamination. Hence, rain water samples were collected at Sinhagad (18°21N, 73°45E, 1450 m asl during the monsoon season (June-September) of 1992 and were analysed for major ions. The precipitation samples collected at Sinhagad were alkaline in nature and pH values ranged between 5.9 to 6.76. The ionic composition was dominated by soil dust The concentration of Ca²⁺ was highest among all the ions. The concentrations of excess SO₃ ^2– and NO₄ ^– were small (23.8 and 15.2 eq l^–1 respectively) compared to the values of polluted regions in India. The correlation coefficient between the ions and pH values was calculated and it was found to be maximum in case of Ca²⁺. Precipitation samples collected at Sinhagad were alkaline owing to higher concentration of Ca²⁺ and lower levels of acidic pollutants (SO₄ ^2– and NO₃ ^–).     

Export of Dissolved Inorganic Nitrogen in a Partially Cultivated Subtropical Mountainous Watershed in Taiwan

A spatial and temporal investigation of dissolved inorganic nitrogen (DIN; NO₃, NO₂ and NH₄) was conducted under various water discharge conditions in Lanyang-Hsi, a subtropical mountainous stream, which drains through distinct degrees of agriculture-influenced sub-watersheds. In both the cultivated and non-cultivated sub-watersheds, NO₃ was the most abundant species accounting for >80% of total DIN, while NH₄ and NO₂ accounted for <15% and=" 5%=" of=" din,=" respectively.=" agricultural=" activities=" along=" the=" riverbank=" led=" to=" significantly=" higher=">₃ concentrations (13–246 M) and DIN yields (1300–3800 kg N km^–2 yr^–1) in main channel when compared to those of non-cultivated tributaries (9–38 M for NO₃ and 550–740 kg N km^–2 yr^–1 for yield). The much lower and less variable DIN yields observed in tributary stations (mean = 660 ± 120 kg N km^–2 yr^–1) are considered as the present day background of DIN yield, which is significantly higher than those of most natural watersheds in other regions. Elevated atmospheric DIN deposition is likely the cause for the high background DIN yield. Human activity within the watershed results in additional DIN yield, which accounted for 49% of total N export. However, the reported atmospheric DIN input in northern Taiwan (1800 kg N km^–2 yr^–1) is much higher than the background DIN yield implying that a major fraction (70%) of atmospheric inputs are retained or processed within the watershed. A dilution pattern occurred in the main channel where high NO₃ concentrations from the upstream sources decreased significantly in downstream direction due to inputs of NO₃-diluted water from non-cultivated areas. We adopted a two-source mixing model to predict the NO₃ dilution pattern. This model revealed a third yet not recognized N source in the lower part of watershed. Model results also indicated the importance of water discharge rate in regulating the relative contribution to total DIN export among these sources.     

Effect of the insecticide methidathion on agricultural soil microflora

Summary We studied the effects of the organophosphorus insecticide methidathion, at concentrations of 10, 50, 100, 200 and 300 g g^-1 in an agricultural soil, on fungi, total bacterial populations, aerobic N₂-fixing bacteria, denitrifying bacteria, nitrifying bacteria (phases I and II), and nitrogenase activity (acetylene reduction assay). The presence of 10–300 g g^-1 of methidathion significantly increased fungal populations (colony-forming units). Denitrifying bacteria, aerobic N₂-fixing bacteria and N₂ fixation were significantly increased at concentrations of 50–300 g g^-1. The total number of bacteria increased significantly at concentrations of 100–300 g g^-1. Nitrifying bacteria decreased initially at concentrations of 300 g g^-1, but recovered rapidly to levels similar to those in the control soil without the insecticide.     

Interactions between anthropogenic sulphate and marine salts in the Bs horizons of acidic soils in Scotland

In laboratory adsorption experiments, the comparison of podzol Bs horizons from coastal and inland moderately-impacted catchments with those from a severely-acidified inland region has demonstrated the effect of marine inputs on SO₄ ^2– -retention. Moderate sea-salt inputs and low acid deposition leads to the retention of most of the SO₄ ^2– and the release of soluble Mg²⁺; increasing the marine salt loading causes the development of a selectivity towards retention of acidic SO₄ ^2– and the retention of Mg²⁺. In the highly-impacted soil, the marine input caused a decrease in SO₄ ^2– retention in open moorland soils. The opposite occurred under forest, due to the ion-exchange of marine Mg²⁺ for soil Al³⁺, increasing soil acidity towards the pH₀ (Gillman and Uehara, 1980), which is depressed below that of its moorland equivalent.     

Synthesis of 15N-labelled microbial biomass in soil in situ and extraction of biomass N

Summary A Pakistani soil (Hafizabad silt loam) was incubated at 30°C with varying levels of ¹⁵N-labelled ammonium sulphate and glucose (C/N ratio of 30 at each addition rate) in order to generate different insitu levels of ¹⁵N-labelled microbial biomass. At a stage when all of the applied ¹⁵N was in organic forms, as biomass and products, the soil samples were analysed for biomass N by the chloroform (CHCl₃) fumigation-extraction method, which involves exposure of the soil to CHCl₃ vapour for 24 h followed by extraction with 500 mM K₂SO₄. A correction is made for inorganic and organic N in 500 mM K₂SO₄ extracts of the unfumigated soil. Results obtained using this approach were compared with the amounts of immobilized ¹⁵N extracted by 500 mM K₂SO₄ containing different amounts of CHCl₃. The extraction time varied from 0.5 to 4 h.The amount of N extracted ranged from 27 to 270 g g^–1, the minimum occurring at the lowest (67 g g^–1) and the maximum at the highest (333 g g^–1) N-addition rate. Extractability of biomass ¹⁵N ranged from 25% at the lowest N-addition rate to 65%a for the highest rate and increased consistently with an increase in the amount of ¹⁵N and glucose added. The amounts of both soil N and immobilized ¹⁵N extracted with 500 mM K₂SO₄ containing CHCl₃ increased with an increase in extraction time and in concentration of CHCl₃. The chloroform fumigation-extraction method gives low estimates for biomass N because some of the organic N in K₂SO₄ extracts of unfumigated soil is derived from biomass.     

Morphological responses among crop species to full-season exposures to enhanced concentrations of atmospheric CO2 and O3

Field studies using open-top chambers were conducted at USDA-BARC involving the growth of soybeans ('89 & '90), wheat ('91 & '92), and corn ('91), under increased concentrations of atmospheric CO₂ and O₃. Treatment responses were compared in all cases to plants grown in charcoal-filtered (CF) air (seasonal 7-h mean = 25±3 n mol O₃ mol^–1) having 350 or 500 mol CO₂ mol^–1. Elevated seasonal O₃ levels for the soybean, wheat, and corn studies averaged 72.2±4, 62.7±2, and 70.2 n mol O₃ mol^–1, respectively. Results presented were obtained for plants grown in silt loam soil under well-watered conditions. Grain yield increases in response to elevated CO₂ in the absence of O₃ stress averaged 9.0, 12.0, and 1.0% for soybean, wheat, and corn; respectively. Reductions in grain yields in response to the elevated O₃ treatments at 350 mol CO, mol^–1 averaged 20.0, 29.0 and 13.0% for soybean, wheat, and corn, respectively. Reductions in grain yields in response to elevated O₃ at 500 mol CO₂ mol^–1 averaged 20.0, 8.0, and 7.0% for soybean, wheat, and corn, respectively. Dry biomass and harvest index in wheat were significantly reduced by O₃ stress at 350 mol mol ¹ CO₂ but not at 500 u mol mol^–1 CO₂. Seed weight 1000^–1 for scybeans and wheat was significantly increased by CO₂ enrichment and decreased by O₃ stress. Seed weight 1000^–1 in corn was increased by O₃ stress suggesting that O₃ affected pollination resulting in fewer kernels per ear.Scientific Article No. A7784, Contribution No. 9105, Maryland Agric. Exp. Sta., Univ. of MD, College Park, MD 20472     

Technetium-99 toxicity in phaseolus vulgaris: Ultrastructural evidence for metabolic disorders

The influence of light intensity on the effects of 10^–6 mol L^{–1 99}Tc on growth, chlorophyll and carotenoid contents of bush bean plants was investigated. After germination and cotyledon excision, the plants were grown in a growth chamber either under low light (photosynthetic active radiation, PAR 144 E m^–2 s^–1) or higher light (PAR 307 E M^–2 s^–1) conditions. In plants grown under the higher light conditions, ⁹⁹Tc hardly affected CO₂-assimilation, dark respiration, pigment contents and growth. No toxicity symptoms were observed in these plants. Under low light conditions, ⁹⁹T c significantly decreased growth and the concentration of chlorophylls. Toxicity symptoms in the form of chlorosis and necrosis developed. Transmission electron microscopy (TEM) observations revealed alterations of chloroplast ultrastructure comparable to those described for plants slightly affected by paraquat toxicity or by Mo-deficiency. Our results indicate that in the low light plants ⁹⁹Tc induces damage in chloroplasts by peroxidation of membrane lipids.     

Seasonal changes and the effects of fertiliser on some chemical,biochemical and microbiological characteristics of high-producing pastoral soil

Summary A 2-year study (1983–1984 to 1984–1985) was conducted to estimate temporal and seasonal changes and the effects of fertiliser on some soil chemical, biochemical and microbiological characteristics. The soil used was a Typic Vitrandept under grazed pasture. Soil samples were taken regularly to a depth of 75 mm from paired unfertilised and fertilised (500 kg ha^– 30% potassic superphosphate) plots. Except for organic C, fertiliser had little or no effect on the characteristics measured. Organic C averaged about 9.2% in unfertilised soil and was about 0.3% higher in the fertilised soil. The size of the microbial biomass fluctuated widely in the 1st year (3000 g C g^–1 in February to 1300 g C g^–1 in September) but there was less variation in the 2nd year (range 1900 g C g^–1 to 2500 g C g^–1 soil). CO₂ production values (10- to 20-day estimates averaged 600 g of CO₂-C g^–1 soil) were generally higher in spring compared to the rest of the year. Water extractable C increased over winter and declined through spring in both years (range 50 g C g^–1 soil to 150 g C g^–1 soil). Mineral-N flush values were higher in summer (300 g N g^–1 soil) and lower in winter months (200 g N g^–1 soil). The pattern of variation of microbial N values was one of gradual accumulation followed by rapid decline. This rapid decline in values occurred in spring and autumn (range 130–220 g N g^–1 soil). N mineralisation and bicarbonate-extractable N showed no clear trend; these values ranged from 100–200 and 122–190 g N g^–1 soil, respectively. There was a significant correlation (0.1%) between N mineralisation and bicarbonate-extractable N in the late summer-autumn-early winter period (February–August) in both years but not in spring. These results and their relationships to climatic factors and rates of pasture production are discussed.     

The “shenandoah national park: Fish in sensitive habitats” (SNP: FISH) project. An integrated assessment of fish community responses to stream acidification

The Shenandoah National Park: Fish in Sensitive Habitats (SNP:FISH) project is a response to declining pH and acid neutralizing capacity in Shenandoah National Park (SNP) streams. SNP receives more atmospheric sulfate than any other USA national park, and pH had decreased to the point where early negative effects on fish were expected. SNP provides the opportunity to study the early stages of acidification effects on fish. Three different classes of geological formations yield streams with low-ANC (0 Eq/L), intermediate-ANC (60–100 Eq/L) or high-ANC (150–200 Eq/L) waters in SNP. This allows a comparison of responses across a water quality gradient in a small geographic area receiving similar deposition. Both chronic and episodic acidification occur in SNP streams. Biological effects are apparent in fish species richness, population density, condition factor, age, size, and bioassay survival. A primary project objective was to provide the necessary data for development and testing models for forecasting changes in fish communities resulting from changes in stream chemistry. Monitored variables include several which are predictive of acidification effects on SNP fish communities.     

Throughfall deposition of ammonium and sulphate during ammonia fumigation of a scots pine forest

The estimation of the dry deposition of sulphur dioxide to forests is confounded by the possibility of co-deposition of SO₂ with NH₃ on leaf surfaces. A sector of Scots pine forest was selectively fumigated with NH₃ to give average concentrations up to 15 ppbV (nL L^–1) above ambient, in order to test the hypothesis that increased air concentrations of NH₃ would enhance the dry deposition of SO₂, and the consequent amounts of SO₄ ^2– measured in throughfall below the forest canopy. Ammonia gas, generated by evaporation of concentrated aqueous solution, was released above the canopy in proportion to wind speed when the wind direction was between south and west. Concentrations of NH₃ at canopy height were measured using passive diffusion tubes; throughfall was preserved with thymol and measured weekly. Meteorological data and SO₂ concentrations were recorded continuously, to permit the estimation of dry deposition input. Deposition of NH₄ ⁺ in throughfall over 8 months was increased by up to 40 meq m^–2 relative to control sites upwind of the NH₃ release point, with largest values closest to the release point. Deposition of SO₄ ^2– in throughfall was also enhanced in the fumigated area, by up to 20 meq m^–2, even though average ambient SO₂ concentrations were 2.3 ppbV. The results are discussed in terms of the factors controlling SO₂ deposition on forest surfaces, the development of appropriate deposition models, and their relevance to using throughfall as an estimate of total S deposition.     

Uptake and toxicity of copper and zinc for the African earthworm,Eudrilus eugeniae (Oligochaeta)

Growth rate change in earthworms is considered to be a suitable endpoint when determining sublethal effects. In this study we evaluated growth and maturation in the vermicomposting earthworm speciesEudrilus eugeniae as marker of sublethal toxicity of copper and zinc. We also compared routes of uptake. Apart from exposing worms experimentally for 73 days to contaminated food, a series of contact filter paper tests was also performed to determine LD₅₀ for copper and zinc. Both copper and zinc at sublethal concentrations affected growth and maturation in worms exposed to contaminated food. These worms had a copper content of 34.5 g g^–1 after 73 days and a zinc content of 184.9 g g^–1, showing a differential uptake. Copper was more toxic than zinc. Also in the contact test worms did take up more zinc than copper and the LD₅₀ (48 h) for copper was 0.011 mg cm^–2 and for zinc 0.066 mg cm^–2, which translated to body burdens of 6 g g^–1 for copper and 131 g g^–1 for zinc. Indications were that a regulatory mechanism existed for both metals. Both metals were taken up through the body wall at a relatively fast rate. This study indicated that the skin was the major route of metal uptake. This study also showed a poor relation between the two types of tests for purposes of evaluating lethality of zinc and copper.