Using Fallout Lead-210 Measurements to Estimate Soil Erosion in Three Small Catchments in Southern Italy

Soil erosion and associated off-site environmental impacts have attracted increasing attention in recent decades, and there is a growing need for reliable information on rates of soil loss. The potential for using ¹³⁷Cs fallout to quantify rates and patterns of soil redistribution over medium-term timescales (ca. 45 years) has been successfully demonstrated in a wide range of environments around the world. The similar behaviour of fallout ²¹⁰Pb in soils offers potential for its use as an alternative to ¹³⁷Cs, in areas where ¹³⁷Cs inventories are low or are complicated by additional fallout from the Chernobyl accident. There have, however, to date been few attempts to validate the use of fallout ²¹⁰Pb measurements for assessing erosion rates. This paper reports an attempt to explore the use of fallout ²¹⁰Pb to estimate rates of water-induced soil erosion on uncultivated land. It focuses on three small forest/rangeland catchments located in Calabria, southern Italy, for which measurements of sediment output are available. Comparison of the estimates of net soil loss from the catchments derived from ²¹⁰Pb measurements with the measured sediment output, confirmed the validity of the ²¹⁰Pb approach. The soil redistribution rates estimated using ²¹⁰Pb measurements were also consistent with equivalent estimates obtained for the same study catchments using ¹³⁷Cs measurements.     

The Input and Transmission of Fallout Radionuclides Through Redó, a High Mountain Lake in the Spanish Pyrenees

Fallout radionuclides have increasing value as tracers of pathways for pollutant transport through catchment/lake systems, in addition to their more traditional role in dating sediment records. The objectivesof this study, carried out within the EU MOLAR project, were tomeasure atmospheric fluxes of fallout ²¹⁰Pb, ¹³⁷Cs and ⁷Be at Redó, to establish mass balances for theseradionuclides, and test and validate models of pollutant transport through the lake and its catchment. This was achieved by comparing measured fluxes and concentrations in the water column with theoretical estimates using simple compartment models. Several interesting points emerged. Differences betweensoil core and rainwater measurements suggest that Saharan dust may be an important source of fallout ²¹⁰Pb. Fluxes throughthe water column had a clear seasonal trend reflecting winter icecover. Significant concentrations of ¹³⁷Cs are still presentin the water column, due to continued inputs from the catchment and/or remobilisation from the bottom sediments.     

Atmospheric Transfer and Deposition Mechanisms of 210Pb Aerosols onto Forest Soils

Activities of ²¹⁰Pb carrier aerosols in an age-graded Sitka spruce conifer, three deciduous (oak, lime and sycamore) foliage and in rain and throughfall samples have been measured during the period of 2001–2002. The ²¹⁰Pb concentrations in the age-graded Sitka leaf needles have shown to accumulate until a steady state between accretion and loss of particulate matter is maintained with time. Similarly, the concentrations of ²¹⁰Pb on deciduous tree leaves increased with time until the leaves began to senesce. The ²¹⁰Pb inventory in bulk precipitation was significantly (r ²?=?0.99; P?<?0.001) large compared with that in throughfall samples, as indicated by a ratio of 1 to 0.1 of ²¹⁰Pb deposition in bulk precipitation to throughfall. This suggests that ²¹⁰Pb is retained in the Sitka spruce foliage during deposition until transfer to the ground mainly through litterfall. These findings suggest that the presence of woodland is responsible for enhanced ²¹⁰Pb deposition fluxes beneath wooded areas relative to open grassland soils.     

Concentrations and Pools of Heavy Metals in Urban Soils in Stockholm,Sweden

The concentrations of heavy metals (Cd, Cr, Cu, Hg, Ni, Pb andZn) and arsenic (As) were surveyed and the metal pools estimatedin soils in Stockholm Municipality. The sampling sites were distributed all over the entire municipality with a higher sampling density in the city centre. Soils were sampled to a maximum depth of 25 to 60 cm. Soil texture, total-C content, electrical conductivity and pH were analysed. Heavy metal concentrations were determined after wet digestion with boiling7 M HNO₃.The results showed a wide range in heavy metal concentrations, as well as in other soil properties. The city centre soils constituted a rather homogeneous group whereas outside this areano geographical zones could be distinguished. These soils were grouped based on present land use, i.e. undisturbed soils, public parks, wasteland (mainly former industrial areas), and roadside soils. The city centre and wasteland soils generally hadenhanced heavy metal concentrations to at least 30 cm depth compared to park soils outside the city centre and rural (arable)soils in the region, which were used to estimate background levels. For example, the mean Hg concentration was 0.9 (max 3.3)mg kg^-1 soil at 0–5 cm and 1.0 (max 2.9) at 30 cm depth in the city centre soils, while the background level was 0,04 mg kg^-1. Corresponding values for Pb were 104 (max 444) and135 (max 339) mg kg^-1, at 0–5 and 30 cm, respectively, while the background level was 17 mg kg^-1.The average soil pools (0–30 cm depth) of Cu, Pb and Zn were 21,38 and 58 g m^-2 respectively, which for Pb was 3–4 timeshigher and for Cu and Zn 1.5–2 times higher than the backgroundlevel. The total amount of accumulated metals (down to 30 cm)in the city centre soils (4.5^*10 ⁶ m² public gardens and green areas) was estimated at 80, 1.1, 120 and 40 t for Cu, Hg, Pb and Zn, respectively. The study showed (1) thatfrom a metal contamination point of view, more homogeneous soilgroups were obtained based on present land use than on geographicdistance to the city centre, (2) the importance of establishing a background level in order to quantify the degree of contamination, and (3) soil samples has to be taken below the surface layer (and deeper than 30 cm) in order to quantify theaccumulated metal pools in urban soils.     

What Anthropogenic Radionuclides (90Sr and 137Cs in Atmospheric Deposition, Surface Soils and Aeolian Dusts Suggest for Dust Transport over Japan

Currently, atmospheric anthropogenic radionuclides (particulate) are controlled by suspension of the surface dust containing those radionuclides (resuspension). We have found, therefore, that such radionuclides can be used as tracers of the surface dust suspension, transport and its subsequent deposition in distant areas. The ¹³⁷Cs/⁹⁰Sr activity ratios in the atmospheric deposition, without the direct influence of nuclear tests and accidents, at the Meteorological Research Institute (MRI, Tsukuba, Japan) during the 1990s were fairly low (average: 2.1). This value is not in agreement with the ratios in Japanese surface soils (range of averages: 4–7), which had been considered as the primary source of the deposited dust. This suggests that the current atmospheric dust deposition in Japan is a mixture of local and remote components. The remote component could be an aeolian dust that has been transported long distances from arid areas. The major component is most likely to be Asian dust. It was further hypothesized that other remote source may exist beyond the Asian domain, based on accumulated observations and model results. To obtain more information about the dust transport, Sahara dust deposited in Monaco in 2002 and a suspended dust collected in the Taklamakan area in 2001 were analyzed for ⁹⁰Sr and ¹³⁷Cs. The Taklamakan dust exhibited a ¹³⁷Cs/⁹⁰Sr ratio of about 4, which is within the range of atmospheric deposition observed at the MRI, while the Sahara dust exhibited a higher ¹³⁷Cs/⁹⁰Sr ratio (about 13). Although the present Sahara datum was negative for our hypothesis of ‘hyper-range transport’, the seasonal change of the ¹³⁷Cs/⁹⁰Sr ratio in the atmospheric deposition observed at the MRI requires an aeolian dust source having a low ¹³⁷Cs/⁹⁰Sr ratio, other than Asian dust.     

Measuring Aerosol and Heavy Metal Deposition on Urban Woodland and Grass Using Inventories of 210Pb and Metal Concentrations in Soil

The deposition of aerosols to trees has proved very difficult to quantify, especially in complex landscapes. However, trees are widely quoted to be efficient scavengers of particles from the atmosphere, and a growing proportion of the pollutant burden in the atmosphere is present in the aerosol phase. In this study, the deposition of aerosols onto woodland and grass was quantified at a range of locations throughout the West Midlands of England. The sites included mature deciduous woodland in Edgbaston, and Moseley, and mixed woodland at sites within Sutton Park, a large area of semi-natural vegetation. Aerosol deposition to areas of grassland close to the woodland at each site was also measured. Detailed inventories of ²¹⁰Pb in soils within the woodland and in grassland soils, together with concentrations in the atmosphere and precipitation, provided the necessary data to calculate the long-term (about 40 years) annual deposition of sub-micron aerosols onto grassland and woodland. The soil inventories of ²¹⁰Pb under woodland exceeded those under grass, by between 22% and 60%, with dry deposition contributing 24% of the total input flux for grass and 47% for woodland. The aerosol dry deposition velocity to grassland averaged 3.3 mm s^-1 and 9 mm s^-1 for woodland. The large deposition rates of aerosols onto woodland relative to grass or other short vegetation (× 3), and accumulation of heavy metals within the surface horizons of organic soils, leads to large concentrations in soils of urban woodland. Concentrations in the top 10 cm of these woodland soils averaged 252 mg kg^-1 for Pb with peaks to 400 mg kg^-1. Concentrations of Cd averaged 1.4 mg kg^-1, Cu, 126 mg kg^-1, Ni 23 mg kg^-1 and Zn 173 mg kg^-1. The accumulated Pb in urban woodland soils is shown to be large relative to UK emissions.     

Fate and behavior of metal(loid) contaminants in an organic matter-rich shooting range soil: Implications for remediation

This study investigates the fate and behavior of lead (Pb), copper (Cu), antimony (Sb), and arsenic (As) in a shooting range soil. The soil samples were collected from the surface (0–15 cm) and the subsurface (15–40 cm and 40–55 cm) of a grassy and wood chip covered impact area behind a firing position. Optical microscopy images indicate significant amounts of corroded bullet fragments and organic wood chips in the surface soil. Analysis by X-ray powder diffraction (XRPD) and scanning electron microscopy electron dispersive X-ray spectroscopy (SEM-EDS) showed that metallic Pb was transformed into lead oxides (litharge PbO and massicot PbO) and lead carbonates (hydrocerussite Pb₃(CO₃)₂(OH)₂, cerussite PbCO₃, and plumbonacrite Pb₅(CO₃)₃O(OH)₂). Rietveld quantification indicated the surface soil contained 14.1% metallic Pb, 17.9% hydrocerussite, 5.2% plumbonacrite, 5.9% litharge, and 3.9% massicot on a dry weight basis, or a total of 39.7% Pb, far in excess of lead concentrations typically found in US shooting range soils. Metallic Cu (bullet jacket material) appeared stable as no secondary minerals were detected in the surface soil. As and Sb concentrations were on the order of 1,057 mg/kg and 845 mg/kg respectively. The elevated soil pH coupled with high organic carbon content is thought to have caused downward migration of metals, especially for Pb, since 4,153 mg Pb/kg was observed at a depth of 55 cm. More than 60% of Pb was concentrated in the coarse soil (> 0.425 mm) fraction, suggesting soil clean-up possible by physical soil washing may be viable. The concentrations of Pb, As, and Sb in the toxicity characteristic leaching procedure (TCLP) extracts were 8,869 mg/L, 6.72 mg/L, and 6.42 mg/L respectively, were above the USEPA non-hazardous regulatory limit (As and Pb) of 5 mg/L. The elevated Sb and As concentrations draw concern because there is historically limited information concerning these metals at firing ranges and several values exceeded local soil cleanup criteria. As the high Pb concentrations appeared to be linked to the presence of organic-rich berm cover materials, the use of wood chips as berm cover to prevent soil erosion requires reconsideration as a shooting range management practice.     

Vertical Distribution of Atmospheric Pollution Lead in Swedish Boreal Forest Soils

In order to understand the fate of anthropogenic lead (Pb)pollution in boreal forest soils, and to predict future trends, it is important to know where in the soil the pollution Pb is accumulated and how large the pollution and natural Pb inventories are in different soil horizons. We combined stable Pb isotope (²⁰⁶Pb/²⁰⁷Pb ratios) and concentration analyses to study Pb in podzol profiles and mor samples from old-growth forest stands at seven sites distributed from southern to northern Sweden. Additional samples were taken from managed forests, and from an agricultural field, to give some idea of the effects of land-use. Pb concentrations are typically 60–100 g g^-1 dry mass in the mor layer in southern Sweden and about 30 g g^-1 in northern Sweden. Pb isotope analyses show that virtually all of this Pb is pollution Pb. The isotope composition also shows that pollution Pb has penetrated downwards between 20–60 cm in the forest soils. The total pollution Pb inventories vary between 0.7–3.0 g m^-2 ground surface, with larger inventories in southern compared to northern Sweden. Although the highest Pb concentrations occur in the mor layer, the largest inventories of pollution Pb are found in the Bs-horizon. The limited investigation of Pb distribution and inventories in soils from managed forests did not point to any major difference compared to the old-growth forests. The agricultural field revealed, however, a completely deviating Pb profile with all pollution Pb evenly distributed in the 20 cm thick top-soil.     

Investigation of gamma ray absorption levels of composites produced from copper mine tailings,fly ash,and brick dust

To date, heavyweight concretes have been produced from various heavy aggregates as radiation insulation materials, and their gamma ray absorption levels have been investigated. Many of the studies have used heavy aggregates instead of cement or coarse aggregates from composite material components. The present study prepared lightweight concretes using copper mine tailings, clay brick dust, and fly ash instead of fine aggregates. Some mechanical tests (density, compressive strength, and ultrasonic pulse velocity) were performed on composite blocks with dimensions of 5*5*5 cm, and radiation interaction parameters [linear absorption coefficient (cm⁻¹), mass attenuation coefficient (cm²/gr), HVL (half-value layer) (cm), MFP (cm), and permeability (%)] were measured. Radiation interaction parameters were obtained using a HPGe gamma detector. Radiation measurements were performed at five different photon energies: 583 keV (¹³³Ba), 609 keV (¹³³Ba), 662 keV (¹³⁷Cs), 911 keV (133^Ba), 1173 keV (⁶⁰Co), and 1332 keV (⁶⁰Co). Additionally, the compressive strength and UPV values of composite materials were associated with their gamma ray permeability. Tests revealed that samples with the addition of copper mine tailings yielded the best energy absorption at all energy levels and that absorption decreased as the energy level increased. For example, with the increasing of the energy level, mass attenuation coefficients decreased. The highest mass attenuation coefficients were obtained as 0.128 cm²/g at an energy level of 583 keV in composites produced from copper mine tailings. On the other hand, it was measured at the same energy level as 0.069 cm²/g (a 46% decrease) in the composites produced with fly ash. In addition, it was observed that fly ash used as a fine aggregate did not have a significant effect on mass attenuation coefficient and could be used as a gamma shield if the material thickness was increased to an average of 14 cm. This study revealed that tailings materials could be used as radiation shields. This study also demonstrated that not using heavy aggregates and producing lightweight concrete in radiation shield production significantly reduced shield production cost.

     

Water movement through an experimental soil liner

A field-scale soil liner was constructed to test whether compacted soil barriers in cover and liner systems could be built to meet the U.S. EPA saturated hydraulic conductivity requirement (⩽ 1 × 10⁻⁷ cm s⁻¹). The 8 × 15 × 0.9 m liner was constructed in 15 cm compacted lifts using a 20,037 kg pad-foot compactor and standard engineering practices. Water infiltration into the liner has been monitored for one year. Monitoring will continue until water break through at the base of the liner occurs. Estimated saturated hydraulic conductivities were 2.5 × 10⁻⁹, 4.0 × 10⁻⁸, and 5.0 × 10⁻⁸ cm s⁻¹ based on measurements of water infiltration into the liner by large- and small-ring infiltrometers and a water balance analysis, respectively.Also investigated in this research was the variability of the liner's hydraulic properties and estimates of the transit times for water and tracers. Small variances exhibited by small-ring flux data suggested that the liner was homogeneous with respect to infiltration fluxes. The predictions of water and tracer breakthrough at the base of the liner ranged from 2.4–12.6 y, depending on the method of calculation and assumptions made. The liner appeared to be saturated to a depth between 18 and 33 cm at the end of the first year of monitoring. Transit time calculations cannot be verified yet, since breakthrough has not occurred. The work conducted so far indicates that compacted soil barriers can be constructed to meet the saturated hydraulic conductivity requirement established by the U.S. EPA.     

Laboratory stabilization/solidification of surrogate and actual mixed-waste sludge in glass and grout

Grout and glass formulations were developed for the stabilization of highly radioactive tank sludges. These formulations were tested in the laboratory with a surrogate and with a sample of an actual mixed waste tank sludge. The grout formulation was tested at wet-sludge loadings of 50–60 wt%, giving a volume increase of about 40–50 vol%. Dried sludge was vitrified into glass at waste oxide loadings of 40–50 wt%, giving a volume decrease of about 50–60 vol%. The Resource Conservation and Recovery Act (RCRA) metals included in surrogate testing were Ag, Ba, Cd, Cr, Ni, Pb, Se, Tl and Hg. Since vitrification would volatilize, not stabilize mercury, it was not included in the surrogates vitrified. The actual sludge sample was only characteristically hazardous for mercury by the toxic characteristic leaching procedure (TCLP) but exceeded the Universal Treatment Standard (UTS) limit for chromium. The grout and glass formulations stabilized these RCRA metals within UTS limits. In addition, a grout leachability index of about 9–10 was measured for both ⁸⁵Sr and ¹³⁷Cs, meeting the recommended requirement of >6. The glass leachability index was estimated to be >18 for cold cesium and strontium.     

Deposition and Fate of Lead in a Forested Catchment, Lesni Potok, Central Czech Republic

The deposition of trace elements and their fate in a forest ecosystemhas been monitored at the experimental site, Lesni Potok catchment (LP), with granite bedrock. The catchment is located 30 km ESE from Prague. Annual bulk Pb-deposition flux F_Pb was 3.41 kg km^-2 a^-1 in 1994 and gradually decreased to 0.49 kg km^-2 a^-1 in 2001. The decrease is comparable with those observed in Germany and in the U.S.A. in the 1970s and 1980s. The total sales ban of leaded gasoline in the Czech Republic since January 2001 was accompanied by a pronounced decrease of F_Pb in a single year. The residual Pb-deposition flux is assigned to both the long-range transport of fine-grained vehicular lead aerosol (with a long residence time in the atmosphere) and to theemissions from power plant boilers burning lignite mined in the Czech northwest coal basin. The F_Pb of lead correlates stronglywith those of As, Cd, Cu, Zn and Be, the typical metals in coal fly ash, at two monitored sites. Topsoil horizons contain elevated concentrations of Pb (53–67 mg kg^-1), which are of anthropogenicorigin. Soils in the riparian areas contain increased concentrations of Pb when compared to soils on the hillslope areas. Significant amounts of Pb were found on a stream substrate and Fe-precipitate sampled from the stream. Low concentrations of Pb in bark and bole wood suggest that the uptake of Pb by vegetation is negligible. The very small surface water outputs (average of 0.002 kg km^-2 a^-1) compared to inputs (average of 1.890 kg km^-2 a^-1) from the LP catchment indicate an ongoing accumulation of Pb in a forested landscape.     

Accumulation of radionuclides released to a reactor discharge pond

Due to material degradation in tubing, the heat exchanger for the primary coolant of the 1 MW Tsing Hua Open-pool Reactor has minor leakage to the secondary cooling system since 1970. In the past 20 years, trace amounts of ^58,60Co, ⁵¹Cr, ¹³⁷Cs, ⁵⁴Mn, ⁴⁶Sc, and ⁶⁵Zn have leaked through the cooling system, accumulated, and eventually trapped in the discharge pond directly in front of the reactor. The distribution of these radionuclides in the mud at different depths and various locations in the pond was measured with standard procedures of radioactive soil sampling and counting techniques. Concentration of corrosion products, with no more than 40 KBq/Kg dry at the hottest spot, was contour-mapped to reveal the accumulation patterns of these trace level radioactive products at the end of the 20-year period.     

Ex‐situ efficacy analysis of brine remediation products in clay loam soil

This study evaluated the effectiveness of gypsum and three proprietary products to remediate brine‐contaminated soil. The research objective was to determine if additives could increase plant cover germination in soils without costly prior soil‐washing or dilution techniques. The soil was shredded using a soil shredder equipped with a spray bar to apply the individual treatments of DeSalt Plus, SoilTech, Chlor*rid, and calcium sulfate (gypsum). Treatments were placed in 40‐mm high‐density polyethylene cells and small drainage systems were installed to allow removal of excess water. An initial 10‐point soil composite was taken from bulk untreated soils at a depth of more than 2.5 cm. Five‐point composite samples were collected from the same depth at weekly intervals and analyzed for: electrical conductivity, sodium adsorption ratio, cation exchange capacity, sodium, calcium, magnesium, potassium, chlorides, and pH. The Gapon selectivity coefficient was calculated and utilized to quantify the affinity for binding between ionic alkali salt constituent groups Na⁺, Ca ⁺⁺, and Mg ^++. Soil analysis indicated product‐related improvements in and bioavailability of salts. The nature of the products requires some prior treatment such as soil washing or dilution using clean soil to lower electroconductivity levels and allow the site to vegetate.     

Spatial variability of soil gas concentration and methane oxidation capacity in landfill covers

In order to devise design criteria for biocovers intended to enhance the microbial oxidation of landfill methane it is critical to understand the factors influencing gas migration and methane oxidation in landfill cover soils. On an old municipal solid waste landfill in north-western Germany soil gas concentrations (10, 40, 90 cm depth), topsoil methane oxidation capacity and soil properties were surveyed at 40 locations along a 16 m grid. As soil properties determine gas flow patterns it was hypothesized that the variability in soil gas composition and the subsequent methanotrophic activity would correspond to the variability of soil properties. Methanotrophic activity was found to be subject to high spatial variability, with values ranging between 0.17 and 9.80 g CH₄ m⁻² h⁻¹_. Considering the current gas production rate of 0.03 g CH₄ m⁻² h⁻¹, the oxidation capacity at all sampled locations clearly exceeded the flux to the cover, and can be regarded as an effective instrument for mitigating methane fluxes. The methane concentration in the cover showed a high spatial heterogeneity with values between 0.01 and 0.32 vol.% (10 cm depth), 22.52 vol.% (40 cm), and 36.85 vol.% (90 cm). The exposure to methane raised the oxidation capacity, suggested by a statistical correlation to an increase in methane concentration at 90 cm depth. Methane oxidation capacity was further affected by the methanotroph bacteria pH optimum and nutrient availability, and increased with decreasing pH towards neutrality, and increased with soluble ion concentration). Soil methane and carbon dioxide concentration increased with lower flow resistance of the cover, as represented by the soil properties of a reduced bulk density, increase in air capacity and in relative ground level.     

Levels and Characteristics of TOC in Throughfall, Forest Floor Leachate and Soil Solution in Undisturbed Boreal Forest Ecosystems

Total organic carbon (TOC) concentrations and fluxes in throughfall, forest floor leachate, soil solution (15 and 35 cm depths), and groundwater for coniferous forest sites in the boreal zone throughout Finland are described. Eight upland forest stands and one peatland forest stand are included in the study and the samples were collected during 1991–1997. Carbon (C) pools in the living tree biomass and soil compartments are presented, and the hydrophobic/hydrophilic and acidic components of dissolved organic carbon (DOC) in samples collected in autumn 1999 and spring 2000 from two of the sites are compared. Biomass (aboveground and belowground) pools of C averaged 88 Mg ha^-1 and soil (humus layer + 20 cm soil layer) averaged 55 Mg ha^-1. Stand throughfall TOC monthly mean concentrations ranged from 4.0 to 18.6 mg L^-1 and annual fluxes averaged 4.0 g m^-2 yr^-1. TOC concentrations in the water passing through the forest floor and soil decreased with depth. Plot mean concentrations at 35 cm depth values ranged from 4.1 to 21.2 mg L^-1 and fluxes averaged 3.7 g m^-2 yr^-1. Throughfall TOC concentrations were lowest during the winter, snowfall period and highest during the growing season. No monotonic trends in throughfall TOC concentrations over the 1991–1997 period were found. Soil solution TOC concentrations varied considerably, both within and between years. DOC in throughfall, forest floor, and soil solutions and in both autumn and spring seasons was dominated by hydrophobic fractions, particularly acids. Spruce canopies and litter appear to be important sources of soluble organic carbon, particularly acidic and hydrophobic compounds. Further studies on the nature and dynamics of organic carbon fluxing through coniferous, boreal forest ecosystems are needed.     

Residual Cadmium and Lead Pollution at a Former Soviet Military Airfield in Tartu, Estonia

This paper presents data on the levels and dynamics of cadmium (Cd) and lead (Pb) concentration in the plants, soil, and groundwater of the landing corridor and airfield of a former Soviet military air base in Estonia, immediately at the end of its 40-year service in 1992 and over the following 8 yr. In 1991–92 we found high Cd concentrations in the meadow plants Trifolium pratense and Dactylis glomerata (up to 56 mg kg^-1). In 1993, the Cd concentration had dropped to 0.12–0.19 mg kg^-1, and stabilized in 1997–2000 at 0.04 mg kg^-1. Cd concentration in plants decreased significantly with increasing distance from the landing strip. Elevated Cd concentration (0.012 mg L^-1) was found in the fuel of the TU-22M (Backfire) strategic bombers. In 1991 and 1993, leaded fuel influenced the mean Pb concentration in plants (1.8–4.2 mg kg^-1). Average Pb concentration in both topsoil and the 30–40 cm soil horizon decreased between 1991 and 2000 from 28 to 6.5 and from 13.5 to 4.3 mg kg^-1, respectively. Cd concentration in the topsoil of the landingcorridor showed a significant increase between 1991 and 1993 (0.07–0.3 and 0.3–1.2 mg kg^-1, respectively), but stabilized later on the level of 0.04 mg kg^-1. The concentrations of both Pb and Cd in the soil were higher closer to the fuel bunkers. Current assessment of the movement of these metals from the vegetation to the soil and to groundwater is linked to potential leaching to the surrounding environment.     

Total Lead and Stable Lead Isotopes in Stockholm Sediments

Lead (Pb) in the environment is derived from both naturaland anthropogenic sources. The aim of this study is to estimate the isotopic signature of anthropogenic Pb in sediments from a highly contaminated area (Stockholm), to discuss the influence of different sources on this signature, and to suggest natural Pb background concentrations. Also distribution patterns and differences between different water areas in Stockholm have been studied, both by total Pb and stable Pb isotopes. In 1993, sediment samples were collected at 24 stations in the Stockholm area and analysed for total Pb, zirconium (Zr), scandium (Sc) and stable Pb isotopes (^{204, 206-208}Pb). Total Pb data show that the Stockholm sediments are severely contaminated by Pb. The contamination seems to be rather local since the small lakes surrounding the central parts of Stockholm are much less effected than the central parts. Stockholm is clearly influenced by anthropogenic and natural sources, but in some of the small lakes also by Pb in zircons from the geological basement. The anthropogenic Pb in Stockholm has typical ²⁰⁷Pb/²⁰⁶Pb ratios of 0.85–0.89 and ²⁰⁸Pb/²⁰⁴Pb ratios of 36–38, which are distinct from natural sources. Pb/Sc ratios suggest that the natural background Pb concentration is 10–20 mg kg^-1 d.w.     

Changing of Lead and Cadmium Pools of Swedish Forest Soils

The aims of the paper are to; i)evaluate the rate and direction of present changesin lead (Pb) and cadmium (Cd) soil pools of Swedishforests; ii) discuss processes of importance forleaching of Pb and Cd in Swedish forest soils. Thepresently ongoing changes of Pb and Cd pools ofSwedish forest soils are evaluated by compilationof data from the literature and unpublishedsources. It is concluded that Cd pools arepresently decreasing in larger areas of Sweden. Therate of decrease is mainly determined by soilacidity status; Cd leaching is regulated by ionexchange with Ca²⁺, Mg²⁺, Al³⁺ andH⁺, and is higher in acid soils. The Pb poolsare presently increasing with 0.1 to 0.3 percentannually in the soil down to 0.5 meter. Pb isredistributed from the O horizon to the B horizon,most pronounced in spruce forests; the Pb pools ofthe O horizon are presently not increasing, but isslightly decreasing by 0.1 to 0.2 percent annually. The leaching of Pb in the soil is controlled byfactors regulating the solubility of organicmatter.     

Simulation of Exterior Conditions in Permanently Closed Soil Chambers by Controlling Air Flow,Soil Water Content,and Temperature

Volatile substances and gases resulting e.g. from degradation processes of chemicals in soils emit into the atmosphere and no chemical mass balance is complete without considering this path. Closed soil chambers allow the evaluation of this transfer to the atmosphere. This study deals with the influence of soil chambers with a glass plate cover on physical soil conditions in the chambers and the possibility to simulate the exterior conditions within the chambers. The water content immediately at the soil surface is an important factor for the microbial activity and the transfer of gaseous compounds to the atmosphere as well. It is monitored by specially designed water content sensors in 1 cm depth in the chamber and as control outside. Funnels with a cross section equal to the soil surface area of the chamber collect the rain water and channel it into the soil chamber. This results in soil water content in the chambers very similar to that outside. For the purpose of analysing ¹⁴CO₂ and volatile ¹⁴C-compounds, air is permanently pumped through the chamber. In order to simulate natural conditions, the wind speed is measured 1 cm above the soil surface outside the chambers. A control circuit adjusts the air flow through the chamber to a value corresponding to the wind speed outside. Temperature measurements in 1 cm depth verify that there is no significant difference between the soil chamber and the control outside.