Three-component model of runoff generation,Lysina catchment,Czech Republic

The forested Lysina catchment is situated in an area very susceptible to acid deposition. The stream water is characterized by extremely high concentrations of total dissolved Al (volume weighted mean 66 Μmol L^?1) and H⁺ (average pH=3.87). In a simple two-component model, the surface runoff component contributes only 6% of runoff in winter and 4% of runoff in summer. During flood episodes, the direct runoff contributes up to 20% of streamflow. There is a strong positive correlation between stream acidity and stream discharge. The observed exponential increase in streamwater acidity with discharge during high flow periods cannot be explained by the simple two-component model. A three-component model used for hydrograph separation is based on chemical and¹⁸O analysis of precipitation, soil water and runoff. It incorporates a soil water component along with groundwater and rainfall components in streamwater generation. Dissociated organic acids leached during the flow of water through the uppermost soil horizon help to balance an apparent anion deficit. The apparent anion deficit was found to increase exponentially with flow rate. Low variability in streamwaterδ ¹⁸O corresponds to a high contribution of indirect components (i.e., soil and ground water) in the runoff. The soil water contribution to indirect runoff calculated from the apparent anion deficit of streamwater, varied from 0 at base flow up to 80% during floods. On average, 40% of the streamwater is derived from soil water (from 31 to 39% in winter and from 47 to 54% in summer).     

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=">     

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

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

Lead Speciation in the Dusts Emitted from Non-Ferrous Metallurgy Processes

The paper presents results for the speciation analysis of lead in dusts derived from dedusting of technological gasses from metallurgical processes of non-ferrous metals with different elementary content, made in accordance with two equal sequential extractions. Analytical procedure A provided possibilities for determination of fraction of Pb(2+), metallic lead and fraction containing mainly lead sulfides. The second procedure (procedure B) was sequential extraction in accordance with Tessier. The results obtained in accordance with procedure A indicate that, regardless of the dust origin, the dominant group of Pb compounds is composed of lead salts which are soluble under alkaline conditions or lead compounds that form plumbites in the reaction with NaOH.