Nitrogen mineralization and CO2 and N2O emissions in a sandy soil amended with original or acidified pig slurries or with the relative fractions

The following six pig slurries obtained after acidification and/or solid/liquid separation were used in the research: original (S) and acidified (AS) pig slurry, nonacidified (LF) and acidified (ALF) pig slurry liquid fraction, and nonacidified (SF) and acidified (ASF) pig slurry solid fraction. Laboratory incubations were performed to assess the effect of the application of these slurries on N mineralization and CO₂ and N₂O emissions from a sandy soil. Acidification maintained higher NH₄ ⁺-N contents in soil particularly in the ALF-treated soil where NH₄ ⁺-N contents were two times higher than in LF-treated soil during the 55–171-day interval. At the end of the incubation (171 days), 32.9 and 24.2 mg N kg⁻¹ dry soil were mineralized in the ASF- and SF-treated soils, respectively, but no mineralization occurred in LF- and S-treated soils, although acidification decreased N immobilization in ALF- (−25.3 mg N kg⁻¹ soil) and AS- (−12.7 mg N kg⁻¹ soil) compared to LF- (−34.4 mg N kg⁻¹ soil) and S-treated (−18.6 mg N kg⁻¹ soil) soils, respectively. Most of the dissolved CO₂ was lost during the acidification process. More than 90% of the applied C in the LF-treated soil was lost during the incubation, indicating a high availability of the added organic compounds. Nitrous oxide emissions occurred only after day 12 and at a lower rate in soils treated with acidified than nonacidified slurries. However, during the first 61 days of incubation, 1,157 μg N kg⁻¹ soil was lost as N₂O in the AS-treated soil and only 937 in the S-treated soil.     

How increasing availabilities of carbon and nitrogen affect atrazine behaviour in soils

 The effect of increasing amounts of glucose and mineral N on the behaviour of atrazine was studied in two soils. One had been exposed to atrazine under field conditions (adapted soil), the other had not (non-adapted soil), resulting, respectively, in an accelerated degradation of atrazine in the adapted soil and in a slow degradation of the herbicide in the non-adapted soil. The dissipation of ¹⁴C-atrazine via degradation and formation of non-extractable "bound" residues was followed during laboratory incubations in soils supplemented or not with increasing amounts of glucose and mineral N. In both soils, glucose added at rates of up to 16 g C kg^–1 soil did not modify atrazine mineralization but increased the formation of bound residues; this was probably due to the retention of atrazine by the growing microbial biomass. Atrazine dealkylation was enhanced when a large amount of glucose was added. In both soils, the addition of the largest dose of mineral N (2.5 g N kg^–1 soil) decreased atrazine mineralization. The simultaneous addition of glucose and mineral N enhanced their effects. When the largest doses of mineral N and glucose were added, atrazine mineralization stopped in both soils, and the proportion of bound residues increased. Glucose and mineral N additions influenced atrazine mineralization to a greater extent in the adapted soil than in the non-adapted one, as revealed by ANOVA, although glucose addition had a greater effect than N. The competition for space and nutrients between atrazine-degrading microorganisms and the total heterotrophic microflora probably contributed to the decrease in atrazine mineralization. Received: 9 June 1998     

Effect of long-term liquid pig manure application on atrazine mineralization in a soil cultivated with maize

Soil samples were collected in plots from a field experiment in maize monoculture receiving 0, 60 and 120 m³ ha^-1 liquid pig manure (LPM) for 19 years. Soils were sampled from the 0- to 20-cm layer in August and October 1997 and in June, July and September 1998. Subsurface samples were also evaluated in September 1998. Laboratory soil radiorespirometry was used to evaluate atrazine mineralization using [U-ring-¹⁴C]-atrazine mixed with commercially available product. The effect of atrazine dose (50, 100 and 500 mg atrazine kg^-1 soil) was evaluated on soils sampled in August 1997. For the other sampling dates, the soils were spiked with 50 mg atrazine kg^-1 soil. No LPM dose effect on atrazine mineralization was obtained in the different experiments. Increasing atrazine dose to 500 mg kg^-1 decreased significantly the mineralization rate (R_i) and the maximum of atrazine mineralized (MAX), while the time needed to mineralize 50% of MAX (DT-50%) was not significantly affected. Sampling time had a significant effect on atrazine mineralization. Atrazine mineralization in the soils sampled in June 1998 showed lower R_i and MAX than in the soils sampled at the other dates. Atrazine mineralization in subsurface soils (20–60 cm) was very variable and quite high in some samples. This may be due to atrazine pre-exposure in subsoils resulting from atrazine deep movement by preferential flow.     

Crop residues and fertilizer nitrogen influence residue decomposition and nitrous oxide emission from a Vertisol

Crop residues with high C/N ratio immobilize N released during decomposition in soil, thus reducing N losses through leaching, denitrification, and nitrous oxide (N₂O) emission. A laboratory incubation experiment was conducted for 84 days under controlled conditions (24°C and moisture content 55% of water-holding capacity) to study the influence of sugarcane, maize, sorghum, cotton and lucerne residues, and mineral N addition, on N mineralization–immobilization and N₂O emission. Residues were added at the rate of 3 t C ha⁻¹ to soil with, and without, 150 kg urea N ha⁻¹. The addition of sugarcane, maize, and sorghum residues without N fertilizer resulted in a significant immobilization of soil N. Amended soil had significantly (P < 0.05) lower NO₃⁻–N, which reached minimum values of 2.8 mg N kg⁻¹ for sugarcane (at day 28), 10.3 mg N kg⁻¹ for maize (day 7), and 5.9 mg N kg⁻¹ for sorghum (day 7), compared to 22.7 mg N kg⁻¹ for the unamended soil (day 7). During 84 days of incubation, the total mineral N in the residues + N treatments were decreased by 45 mg N kg⁻¹ in sugarcane, 34 mg kg⁻¹ in maize, 29 mg kg⁻¹ in sorghum, and 16 mg kg⁻¹ in cotton amended soil compared to soil + N fertilizer, although soil NO₃⁻–N increased by 7 mg kg⁻¹ in lucerne amended soil. The addition of residues also significantly increased amended soil microbial biomass C and N. Maximum emissions of N₂O from crop residue amended soils occurred in the first 4–5 days of incubation. Overall, after 84 days of incubation, the cumulative N₂O emission was 25% lower with cotton + N fertilizer, compared to soil + N fertilizer. The cumulative N₂O emission was significantly and positively correlated with NO₃⁻–N (r = 0.92, P < 0.01) and total mineral N (r = 0.93, P < 0.01) after 84 days of incubation, and had a weak but significant positive correlation with cumulative CO₂ in the first 3 and 5 days of incubation (r = 0.59, P < 0.05).     

Microbial biomass and C mineralization in agricultural soils as affected by atrazine addition

This study examines the effects of atrazine on both microbial biomass C and C mineralization dynamics in two contrasting agricultural soils (organic C, texture, and atrazine application history) located at Galicia (NW Spain). Atrazine was added to soils, a Humic Cambisol (H) and a Gleyic Cambisol (G), at a recommended agronomic dose and C mineralization (CO₂ evolved), and microbial biomass measurements were made in non-treated and atrazine-treated samples at different time intervals during a 12-week aerobic incubation. The cumulative curves of CO₂–C evolved over time fit the simple first-order kinetic model [Ct = Co (1 − e ^−kt )], whose kinetic parameters were quantified. Differences in these parameters were observed between the two soils studied; the G soil, with a higher content in organic matter and microbial biomass C and lower atrazine application history, exhibited higher values of the total C mineralization and the potentially mineralizable labile C pool than those for the H soil. The addition of atrazine modified the kinetic parameters and increased notably the C mineralized; by the end of the incubation the cumulative CO₂–C values were 33–41% higher than those in the corresponding non-added soils. In contrast, a variable effect or even no effect was observed on the soil microbial biomass following atrazine addition. The data clearly showed that atrazine application at normal agricultural rates may have important implications in the C cycling of these two contrasting acid soils.     

Dynamic of organic matter in the heavy fraction after abandonment of cultivated wetlands

The abandonment of cultivated wetland soil increased the contents of light fraction organic matter (LFOM), heavy fraction organic matter (HFOM) and soil organic matter (SOM). The LFOM and HFOM content increased to 13.3 g kg⁻¹ and 62.4 g kg⁻¹ after 5 years whereas they were 8.4 and 47.9 g kg⁻¹ after 9 years of cropping, respectively. Fourteen years after abandonment, HFOM content increased to 104.3 g kg⁻¹. LFOM was positively correlated with HFOM (p < 0.001). A Langmuir equation was used to calculate the highest HFOM value. The value for the natural wetland soil was closed to this theoretical value (140.8 g kg⁻¹). After 14 years of abandonment, the HFOM maximum (HFOM_Max) value was lower than the equilibrium value suggesting that a further increase in HFOM can occur after abandonment. Assuming a linear accumulation (3.87 Mg C ha⁻¹yr⁻¹), it would take approximately 24 years after the abandonment to reach the HFOM_Max value.     

Estimation of sulfur mineralization and relationships with nitrogen and carbon in soils

A 25-week laboratory study was carried out to determine sulfur, carbon, and nitrogen mineralization rates in soil samples obtained from representative soils in France. Their relationship with some of the soil properties was investigated to find a predictor of mineralized S in soils. At 20°C and 80% water-holding capacity, the S mineralization rate ranged from 0.02 to 0.16 mg kg⁻¹ day⁻¹. It was significantly positively related to soil organic C and N and to C and N mineralization rates. It was weakly related to total soil S. The results suggest that the S mineralization is predominantly driven by heterotrophic microbial activity. A predictive equation for S mineralization based on soil C content, soil pH, and clay content is proposed.     

A critical assessment of soil amendments (slaked lime/acidic fertilizer) for the phytomanagement of moderately contaminated shooting range soils

Purpose  

The effects of the addition of an acidic fertilizer solution and/or slaked lime (5.5 g Ca(OH)₂ kg⁻¹) on a slightly acidic shooting range soil (pH 6.1, % organic carbon 5.4) with moderate metal (e.g., 620 mg kg⁻¹ Pb) and metalloid (17 mg kg⁻¹ Sb) concentrations on metal and Sb solubility and plant accumulation were investigated.     

Sequencing Zerovalent Iron Treatment with Carbon Amendments to Remediate Agrichemical-Contaminated Soil

Agrichemical spills and discharges to soil can cause point-source contamination of surface and ground waters. When high contaminant concentrations inhibit natural attenuation in soils, chemical treatments can be used to promote degradation and allow application of treated soils to agricultural lands. This approach was used to remediate soil containing >650 mg atrazine, >170 mg metolachlor and >18,000 mg nitrate kg^?1. Results indicated a decrease in metolachlor concentration to <1 mg kg^?1 within 95 days of chemical treatment with zerovalent iron (Fe⁰, 5% w/w) and aluminum sulfate (Al₂(SO₄)₃, 2% w/w) but after one year >150 mg atrazine and >7000 mg nitrate kg^?1 remained. Laboratory experiments confirmed that subsequent additions of sucrose (table sugar) to the chemically pretreated soil promoted further reductions in atrazine and nitrate concentrations. Field-scale results showed that adding 5% (w/w) sucrose to windrowed and pretreated soil significantly reduced atrazine (<38 mg kg^?1) and nitrate (<2,100 mg kg^?1) concentrations and allowed for land application of the treated soil. These results provide evidence that zerovalent iron in combination with Al₂(SO₄)₃ and sucrose can be used for on-site, field-scale treatment of pesticide- and nitrate-contaminated soil.     

Soil Acid-Base Chemistry of a High-Elevation Forest Watershed in the Great Smoky Mountains National Park: Influence of Acidic Deposition

Understanding the acid-base chemistry of soil and the soil processes related to the release or retention of sulfate and nitrate is important in order to predict watershed recovery from long-term acid deposition. Soils were sampled from the Noland Divide Watershed (NDW), a small, high-elevation watershed in the Great Smoky Mountains National Park receiving high rates of acid deposition over several decades. Soil samples were measured for chemical properties related to acidification and used to conduct sulfate adsorption and nitrogen (N) incubation experiments. Shallow soil was higher in acidic and basic ions than deeper soils, and the mean effective cation exchange capacity was 8.07, 5.06, and 3.57 cmol_c kg⁻¹ in the A, Bw, and Cb horizons, respectively. In all three soil horizons, the base saturation was equal to or below 7% and the ratio of Ca/Al was below 0.01, indicating that the NDW is very sensitive to acid deposition. Based on results from sulfate adsorption isotherms, the NDW has not reached its maximum sulfate adsorption saturation and is likely able to retain further additions of sulfate. Desorption of sulfate from NDW soils is expected if sulfate concentrations in soil solution drop below 50 μeq L⁻¹ but is highly dependent on soil pH and organic carbon content. Total soil organic N was 500 times greater than inorganic N in the A soil horizon, and net N mineralization and nitrification remained constant during a 28-day incubation indicating a large reservoir of N substrate for soil microbes. Nitrogen experiment results suggest that nitrate export from the watershed is largely controlled by biological processes rather than by nitrate deposition flux. Soil data collected in this study contributes to our understanding of biogeochemical processes affecting the response of acid-impacted ecosystems such as the NDW to future changes in atmospheric deposition.     

Biological nitrogen fixation by common beans (<Emphasis Type="Italic">Phaseolus vulgaris</Emphasis> L.) increases with bio-char additions

This study examines the potential, magnitude, and causes of enhanced biological N₂ fixation (BNF) by common beans (Phaseolus vulgaris L.) through bio-char additions (charcoal, biomass-derived black carbon). Bio-char was added at 0, 30, 60, and 90 g kg⁻¹ soil, and BNF was determined using the isotope dilution method after adding ¹⁵N-enriched ammonium sulfate to a Typic Haplustox cropped to a potentially nodulating bean variety (CIAT BAT 477) in comparison to its non-nodulating isoline (BAT 477NN), both inoculated with effective Rhizobium strains. The proportion of fixed N increased from 50% without bio-char additions to 72% with 90 g kg⁻¹ bio-char added. While total N derived from the atmosphere (NdfA) significantly increased by 49 and 78% with 30 and 60 g kg⁻¹ bio-char added to soil, respectively, NdfA decreased to 30% above the control with 90 g kg⁻¹ due to low total biomass production and N uptake. The primary reason for the higher BNF with bio-char additions was the greater B and Mo availability, whereas greater K, Ca, and P availability, as well as higher pH and lower N availability and Al saturation, may have contributed to a lesser extent. Enhanced mycorrhizal infections of roots were not found to contribute to better nutrient uptake and BNF. Bean yield increased by 46% and biomass production by 39% over the control at 90 and 60 g kg⁻¹ bio-char, respectively. However, biomass production and total N uptake decreased when bio-char applications were increased to 90 g kg⁻¹. Soil N uptake by N-fixing beans decreased by 14, 17, and 50% when 30, 60, and 90 g kg⁻¹ bio-char were added to soil, whereas the C/N ratios increased from 16 to 23.7, 28, and 35, respectively. Results demonstrate the potential of bio-char applications to improve N input into agroecosystems while pointing out the needs for long-term field studies to better understand the effects of bio-char on BNF.     

Field-scale variability of topsoil dehydrogenase and cellulase activities as affected by variability of some physico-chemical properties

We have studied spatial field-scale variability of soil dehydrogenase (DH) and cellulase activities (CEL) and their relationship with variability of some physico-chemical properties at the surface horizon of the agricultural field. Soil samples were collected at 50 points from the upper 20 cm of soil. The activity of DH ranged between 0.77 and 1.5 μM TPP·g⁻¹·h⁻¹ while CEL activity ranged from 0.8 to 1.94 μM glucose·g⁻¹·24 h⁻¹. Concentrations of C_ORG and TN varied from 8.5 to 31.7 g·kg⁻¹ and from 0.94 to 3.56 g·kg⁻¹, respectively. The soil data showed that spatial variability and semivariograms describe spherical and linear models with the nugget effect (DH, CEL, C_ORG and TN). Dehydrogenase activity was in the strong variability class, while cellulase activity was situated in the week variability class. Both C_ORG and TN concentrations and pH_KCl values were strongly spatially dependent with the percentage of total variance (sill) presents as nugget variance ranging from 8.9% to 16.1%. Kriged maps displayed the lowest values of CEL activities in the north-east of the area, while the south area showed the highest CEL activity. The DH activity values were irregularly distributed in the surface horizon of the studied soil and this behaviour did not correspond with the spatial distribution of other properties.     

Availability and Accumulation of Arsenic in Oilseeds Grown in Contaminated Soils

Arsenic occurs in the earth's crust in various chemical forms as a result of both natural and anthropogenic sources. Soil chemical extractions may help understand As availability, as well as the possibility of As entry into the food chain. Phytoextraction has been proposed as a technology for remediation of As-contaminated soils. The study was carried out to assess the bioavailability of As by extractants and to compare the performance of castor bean and sunflower for As removal from soils. Two soils were contaminated with Na₂HAsO₄.7H₂O adding 35 and 150 mg As dm⁻³ soil. Arsenic availability was assessed using the following extractants: tri-distilled water, ammonium sulfate, ammonium phosphate, ammonium oxalate + oxalic acid, organic acids mixture, Mehlich-1, and United States Environmental Protection Agency 3051. The roots and shoots of 35-day-old plants were collected and dry matter yield as well as As concentration were determined. The accumulation of As in shoot was also calculated in order to evaluate the plants potential for As phytoextraction. The extractants tested were efficient to assess the concentration of available As in soil. Addition of As to the soils did not cause severe toxicity in plants, although the dose 150 mg As dm⁻³ soil decreased shoot and root yield in both species. Castor bean was less sensitive to As than sunflower, but none of the species had hyperaccumulation characteristics. These species can be used for revegetation of areas contaminated with As up to safe limit of 150 mg As dm⁻³ soil, as proposed by CONAMA for industrial areas in Brazil.     

Importance of heterotrophic nitrification and dissimilatory nitrate reduction to ammonium in a cropland soil: Evidences from a 15N tracing study to literature synthesis

Future climate change is predicted to influence soil moisture regime, a key factor regulating soil nitrogen (N) cycling. To elucidate how soil moisture affects gross N transformation in a cultivated black soil, a ¹⁵N tracing study was conducted at 30%, 50% and 70% water-filled pore space (WFPS). While gross mineralization rate of recalcitrant organic N (N_rec) increased from 0.56 to 2.47 mg N kg⁻¹ d⁻¹, the rate of labile organic N mineralization declined from 4.23 to 2.41 mg N kg⁻¹ d⁻¹ with a WFPS increase from 30% to 70%. Similar to total mineralization, no distinct moisture effect was found on total immobilization of ammonium, which primarily entered the N_rec pool. Nitrate (NO₃⁻) was mainly produced via autotrophic nitrification, which was significantly stimulated by increasing WFPS. Unexpectedly, heterotrophic nitrification was observed, with the highest rate of 1.06 mg N kg⁻¹ d⁻¹ at 30% WFPS, contributing 31.8% to total NO₃⁻ production, and decreased with WFPS. Dissimilatory nitrate reduction to ammonium (DNRA) increased from near zero (30% WFPS) to 0.26 mg N kg⁻¹ d⁻¹ (70% WFPS), amounting to 16.7–92.9% of NO₃⁻ consumption. A literature synthetic analysis from global multiple ecosystems showed that the rates of heterotrophic nitrification and DNRA in test soil were comparative to the forest and grassland ecosystems, and that heterotrophic nitrification was positively correlated with precipitation, soil organic carbon (SOC) and C/N, but negatively with pH and bulk density, while DNRA showed positive relationships with precipitation, clay, SOC, C/NO₃⁻ and WFPS. We suggested that low pH and bulk density and high SOC and C/N in test soil might favor heterotrophic nitrification, and that C and NO₃⁻ availability together with anaerobic condition were crucial for DNRA. Overall, our study highlights the role of moisture in regulating gross N turnover and the importance of heterotrophic nitrification for NO₃⁻ production under low moisture and DNRA for NO₃⁻ retention under high moisture in cropland.     

Effects of long-term compost and fertilizer application on stability of aggregate-associated organic carbon in an intensively cultivated sandy loam soil

The study examined the influence of compost and mineral fertilizer application on the content and stability of soil organic carbon (SOC). Soil samples collected from a long-term field experiment were separated into macroaggregate, microaggregate, and silt + clay fractions by wet-sieving. The experiment involved seven treatments: compost, half-compost N plus half-fertilizer N, fertilizer NPK, fertilizer NP, fertilizer NK, fertilizer PK, and control. The 18-year application of compost increased SOC by 70.7–121.7%, and mineral fertilizer increased by 5.4–25.5%, with no significant difference between control soil and initial soil. The C mineralization rate (rate per unit dry mass) in microaggregates was 1.52–2.87 mg C kg⁻¹ day⁻¹, significantly lower than in macroaggregate and silt + clay fractions (P < 0.05). Specific C mineralization rate (rate per unit SOC) in silt + clay fraction amounted to 0.48–0.87 mg C g⁻¹ SOC day⁻¹ and was higher than in macroaggregates and microaggregates. Our data indicate that SOC in microaggregates is more stable than in macroaggregate and silt + clay fractions. Compost and mineral fertilizer application increased C mineralization rate in all aggregates compared with control. However, compost application significantly decreased specific C mineralization rate in microaggregate and silt + clay fractions by 2.6–28.2% and 21.9–25.0%, respectively (P < 0.05). By contrast, fertilizer NPK application did not affect specific C mineralization rate in microaggregates but significantly increased that in silt + clay fractions. Carbon sequestration in compost-amended soil was therefore due to improving SOC stability in microaggregate and silt + clay fractions. In contrast, fertilizer NPK application enhanced SOC with low stability in macroaggregate and silt + clay fractions.     

Characterization of Swine Wastewater by Toxicity Identification Evaluation Methodology (TIE)

Since swine wastewater is used by farmers for soil fertilization, evaluation of toxic compounds or micro-contaminants of separate streams is required. This paper uses the toxicity identification evaluation (TIE) procedure for the physicochemical and ecotoxicological characterization of swine wastewater. To distinguish the most important toxic compounds, a physicochemical characterization and phase I-TIE procedure were performed. The acute toxic effect of swine wastewater and treated fractions (phase II-TIE) were evaluated using Daphnia magna determining 48-h LC₅₀. Results show a high level of conductivity (23.5 μS cm⁻¹), which is explained as due to the concentration of ions, such as ammonium (NH₄⁺–N 1.6 g L⁻¹), sulfate (SO₄²⁻ 397.3 mg L⁻¹), and chlorine (Cl⁻ 1,230.0 mg L⁻¹). The acute toxicity of the swine wastewater was evaluated on D. magna (48-h LC₅₀ = 3.4%). Results of the different water treatments indicate that anionic exchange treatments could reduce 22.5% of swine wastewater’s acute toxicity by reducing chlorine (to around 51%) and conductivity (8.5%). On the other hand, cationic exchange treatment increased acute toxicity on D. magna (% RT = −624.4%), by reducing NH₄⁺–N (around 100%) and total nitrogen (95.5%). This finding suggests that part of the toxicity comes from anionic compounds, such as chlorine.     

Mineralization of the herbicide MCPA in urban soils is linked to presence and growth of class III tfdA genes

Mineralization and sorption of ¹⁴C-ring labeled herbicide 2-methyl-4-chlorophenoxyacetic acid (MCPA) were quantified along with the tfdA gene abundance in 7 different soils. The soils tested were five gravel soils from urban locations, one soil from the embankment of a railway track, and finally an agricultural soil as a control. The mineralization experiments were performed with a concentration of MCPA of 5 mg/kg and incubated at 10 °C for a period of 60 days.With K_d values ranging from 0.04 to 0.41 l kg⁻¹ the sorption experiments revealed that binding of MCPA to the six gravel soils was lower compared to the control soil which had a K_d value of 0.91 l kg⁻¹. The potential for MCPA mineralization varied from less than 5 to over 55% mineralized in 60 days. The most rapid MCPA mineralization was observed in the soil from the Danish railway tracks with 55% mineralized after only 18 days. The mineralization data was fitted to degradation kinetic models, which indicated that growth occurred as a response to MCPA degradation in most of the soils.Soil DNA was extracted and tfdA genes responsible for the first step in MCPA degradation were quantified by real-time PCR (qPCR) at appropriate time points throughout the mineralization experiments. Indicating growth of specific MCPA degraders, the abundance of class III tfdA genes showed an increase during MCPA mineralization in those soils able to mineralize MCPA.These findings emphasize the importance of the presence of microorganisms that are able to readily degrade MCPA, to avoid groundwater leaching following use on urban gravel areas that possess low binding ability of the compound.     

Plant Availability and Uptake of Lead, Zinc, and Cadmium in Soils Contaminated with Anti-corrosion Paint from Pylons in Comparison to Heavy Metal Contaminated Urban Soils

Red lead (Pb₃O₄) has been used extensively in the past as an anti-corrosion paint for the protection of steel constructions. Prominent examples being some of the 200,000 high-voltage pylons in Germany which have been treated with red lead anti-corrosion paints until about 1970. Through weathering and maintenance work, paint compounds and particles are deposited on the soils beneath these constructions. In the present study, six such “pylon soils” were investigated in order to characterize the plant availability and plant uptake of Pb, Cd, and Zn. For comparison, three urban soils with similar levels of heavy metal contamination were included. One phase extractions with 1 M NH₄NO₃, sequential extractions (seven steps), and extractions at different soil pH were used to evaluate the heavy metal binding forms in the soil and availability to plants. Greenhouse experiments were conducted to determine heavy metal uptake by Lolium multiflorum and Lactuca sativa var. crispa in untreated and limed red lead paint contaminated soils. Concentrations of Pb and Zn in the pylon soils were elevated with maximum values of 783 mg Pb kg⁻¹ and 635 Zn mg kg⁻¹ while the soil Cd content was similar to nearby reference soils. The pylon soils were characterized by exceptionally high proportions of NH₄NO₃-extractable Pb reaching up to 17% of total Pb. Even if the relatively low pH of the soils is considered (pH 4.3–4.9), this appears to be a specific feature of the red lead contamination since similarly contaminated urban soils have to be acidified to pH 2.5 to achieve a similarly high Pb extractability. The Pb content in L. multiflorum shoots reached maximum values of 73 mg kg⁻¹ after a cultivation time of 4 weeks in pylon soil. Lime amendment reduced the plant uptake of Pb and Zn significantly by up to 91%. But L. sativa var. crispa cultivated on soils limed to neutral pH still contained critical Pb concentrations (up to 0.6 mg kg⁻¹ fresh weight). Possible mechanisms for the exceptionally high plant availability of soil Pb derived from red lead paint are discussed.     

Soil Degradation Due to Vicinal Intensive Hog Farming Operation Located in East Mediterranean

One of the main environmental impacts of concentrated animal feeding operations is the soil degradation in vicinity with the livestock breeding facilities due to substances such as ammonia emitted from the various stages of the process. Owing to the high temperatures of the Mediterranean ecosystems, the evolution of gasses is more extensive and the soil degradation is consequently more severe than those obtained in northern Europe. In this research, the soil degradation effects of a large meat-producing, processing, and packaging unit have been investigated. The investigated intensive hog farming operation (IHFO) is located at a limestone soil coastal area with sea to the north and hills to the south. Soil samples of the upper mineral soil were taken in various distances and directions from the IHFO boundaries. Thirteen experimental cycles were carried out in the duration of 1.5 years starting in March 2009 until October 2010. The soil samples were analyzed on pH and electrical conductivity (EC) values as well as NH₄ ⁺ and NO₃ ⁻ concentrations. Significantly higher concentrations of the two nitrogen forms were observed on samples at increasing proximity downwind from the farm (south). Southern soil average NH₄ ⁺ and NO₃ ⁻ concentrations ranged between 0.4–118 μg NH₄ ⁺-N g⁻¹ soil and 6.1–88.4 μg NO₃ ⁻-N g⁻¹ soil, respectively. The variation of emitted gasses depositions was clearly reflected in the average pH and EC values. Average pH and EC values downwind from IHFO boundaries varied between 7.1–8.2 and 140–268 μS/cm, respectively.     

Role of organic fractions on C decomposition and N mineralization of animal wastes in soil

The relative contributions of water-soluble, water-non-soluble, Van Soest-soluble, and neutral detergent fiber (NDF) fractions of pig slurry (PS), cattle slurry (CS), cattle farmyard manure (FYM), and composted cattle farmyard manure (CFYM) to the overall C and N mineralization of the raw wastes were studied by incubating treated soil for 107 days at 15°C under non-limiting N conditions. The C or N mineralization of soluble fractions was calculated from the difference between C or N mineralization of the raw and non-soluble fractions. The organic N content of raw wastes ranged from 15 to 32 mg N g⁻¹ dry matter and organic C to organic N ratio from 13 to 29. The water-soluble fraction (SOL_W) was close to 100 mg C g⁻¹ raw waste C for CS, FYM, and CFYM but reached 200 mg C g⁻¹ for PS. The Van Soest-soluble fraction (SOL_VS) was the main fraction for PS, CS, and CFYM (>500 mg C g⁻¹ raw waste C) but only 303 mg C g⁻¹ raw waste C for FYM. Both soluble and non-soluble fractions contributed to C decomposition of slurries, with half to more than half of the decomposed C derived from the degradation of soluble compounds. Most of the C decomposed from FYM was derived from the large NDF fraction, but the contribution from the water-soluble C to the decomposition was also significant. Carbon mineralization of CFYM was due to the degradation of the NDF fraction, whereas soluble C did not contribute. Amounts of N mineralized or immobilized by raw wastes and non-soluble fractions at the end of incubation were significantly correlated (P < 0.01) with their organic C to organic N ratio. The contribution of the Van Soest-soluble fraction to N mineralization varied greatly between the four wastes. Finally, large differences in the C degradability and N availability of the water and Van Soest-soluble fractions were demonstrated.