A comparison of the convection-dispersion equation and transfer function model for predicting chloride leaching through an undisturbed, structured clay soil

The transfer function mode) (TFM) and convection-dispersion equation (CDE) were compared for predicting Cl ^? transport through a calcareous pelosol during steady, nearsaturated water flow. Large, undisturbed soil cores were used at constant irrigation intensities (q₀) between 0.3 and 3 cm h^?1, with a step-change in Cl^? concentration. The assumption of a lognormal distribution of travel times–characterized by the mean (μ) and variance (σ²)–permitted the flux-averaged breakthrough curves (BTCs) to be modelled very accurately by the TFM. The BTCs could be modelled equally well by the CDE when both the mean pore water velocity (v) and dispersion coefficient (D) were optimized simultaneously by the method of least squares, but not when v was put equal to q₀/_v, where _V was the mean volumetric water content. The best estimate of v was consistently > q₀/_v, which suggested that not all the pore water was effective in chloride transport. An operationally defined transport volume (θ_st) was calculated from the mean () or median (τ_m) travel times derived from the TFM. Chloride exclusion was not solely responsible for θ_st() being <_V: immobile water also contributed. The positive skewness of the travel time distributions meant that θ_st(τ_m) < θ_st(), indicating the effectiveness of macropore flow in solute transport. Dαv^1.42 (from the CDE), and σ²αv (from the TFM), confirmed that Cl^? dispersion increased as flow velocity increased. Flux-averaged concentrations were used to calculate the volume-averaged resident concentrations. They matched the measured Cl^? concentrations most closely when there was a gradual decrease in measured Cl ^? concentration with depth, but not when Cl ^? decreased sharply below c. 10 cm. Calculations assuming that all the water was effective in chloride transport gave less accurate results. Comparison of the measured and predicted concentrations of solute demonstrated that this must be a critical part of the evaluation of any model of solute transport.     

Determination of total soil organic C and hot water‐extractable C from VIS‐NIR soil reflectance with partial least squares regression and spectral feature selection techniques

The calibration of soil organic C (SOC) and hot water‐extractable C (HWE‐C) from visible and near‐infrared soil reflectance spectra is hindered by the complex spectral interaction of soil chromophores that usually varies from one soil or soil type to another. The exploitation of spectral variables from spectroradiometer data is further affected by multicollinearity and noise. In this study, a set of soil samples (Fluvisols, Podzols, Cambisols and Chernozems; n = 48) representing a wide range of properties was analysed. Spectral readings with a fibre‐optics visible to near‐infrared instrument were used to estimate SOC and HWE‐C contents by partial least squares regression (PLS). In addition to full‐spectrum PLS, spectral feature selection techniques were applied with PLS (uninformative variable elimination, UVE‐PLS, and a genetic algorithm, GA‐PLS). On the basis of normalized spectra (mean centring + vector normalization), the order of prediction accuracy was GA‐PLS ? UVE‐PLS > PLS for SOC; for HWE‐C, it was GA‐PLS > UVE‐PLS, PLS. With GA‐PLS, acceptable cross‐validated (cv) prediction accuracies were obtained for the complete dataset (SOC, , RPD_cv = 2.42; HWE‐C_cv, , RPD_cv = 2.13). Splitting the soil data into two groups with different basic properties (Podzols compared with Fluvisols/Cambisols; n = 21 and n = 23, respectively) improved SOC predictions with GA‐PLS distinctly (Podzols, , RPD_cv = 3.14; Fluvisols/Cambisols, , RPD_cv = 3.64). This demonstrates the importance of using stratified models for successful quantitative approaches after an initial rough screening. GA selection frequencies suggest that the spectral region over 1900 nm, and in particular the hydroxyl band at 2200 nm are of great importance for the spectral prediction of both SOC and HWE‐C.     

Soil wetting‐drying and water‐retention properties in a mine‐soil treated with composted and thermally‐dried sludges

The main objective of this study was to analyse how different sewage sludges influence soil wetting and drying dynamics. Three composted and three thermally‐dried municipal sludges from different wastewater plants located in Catalonia (NE Spain) were mixed with a mine‐soil obtained from a limestone quarry. Measurements of the time required to reach zero contact angle () and water holding time (WHT) provided information on the time required for a mine‐soil to reach its complete wettability and the residence time of water stored between ?0.75 and ?25 MPa of soil suction, respectively. One month after sludge amendments, one composted and one thermally‐dried sludge significantly increased . WHT was increased in the mine‐soil treated by composted sludges (50.6% by Blanes' sludge, 65.5% by Manresa's sludge and 52.5% by Vilaseca's sludge) one month after sludge amendments. The amount of water retained in the mine‐soil was increased by all composted sludges and one thermally‐dried sludge after one month (by 42.3% with Blanes' sludge, 42.3% with Manresa's sludge, 65.7% with Vilaseca's sludge and 23.9% with Mataró's sludge) and one year after sludge amendments and at a small suction. Increments in WHT corresponded with the amount of water retained so the time‐scale of soil water availability should also be considered. The value was modified mainly by increments in carbon stock and microbial biomass, while the WHT was modified mainly by increments in pH and electrical conductivity. Under similar air‐drying conditions, mine‐soil treated with composted sludges retained more water for longer compared with thermally‐dried sludges.     

SATURATION PERCENTAGE AS A MEASURE OF SOIL TEXTURE IN THE LOWER INDUS BASIN

The saturation percentage is related to the mechanical constituents of a soil: and is therefore a quantitative expression of soil texture. Profiles may be described in terms of the S.P.; thus Maps may be drawn showing quantitative changes in texture, and associated statements of the reliability of an S.P. estimate and the probable error of the position of a textural contour be made. Decomposition of the calcium carbonate component should be avoided in routine soil survey work.     

Depletion of non‐exchangeable NH$ _4^+ $ at the root–soil and hyphae–soil interface of VA mycorrhizal maize (Zea mays) and parsley (Petroselinum sativum)

Mobilization of non‐exchangeable ammonium (NH ) by hyphae of the vesicular‐arbuscular mycorrhizal (VAM) fungus Glumus mosseae was studied under controlled experimental conditions. Maize (Zea mays) and parsley (Petroselinum sativum) were grown either alone or in symbiosis with Glomus mosseae in containers with separated compartments for roots and hyphal growth. In one experiment, ¹⁵NH was added to the soil to differentiate between the native non‐exchangeable NH and the non‐exchangeable NH derived from N fertilization. Non‐exchangeable NH was mobilized by plant growth. Plant dry weight and N uptake, however, were not significantly influenced by mycorrhizal colonization of the roots. The influence of root infection with mycorrhizal fungus on the mobilization of non‐exchangeable NH was negligible. In the hyphal compartment, hyphal uptake of N resulted in a decrease of NH in the soil solution and of exchangeable NH . However, the NH concentration was still too high to permit the release of non‐exchangeable NH . The results demonstrate that, in contrast to roots, hyphae of VAM fungi are not able to form a non‐exchangeable‐NH depletion zone in the adjacent soil. However, under conditions of a more substantial depletion of the exchangeable NH in the mycorrhizal sphere (e.g., with longer growth), an effect of mycorrhiza on the non‐exchangeable NH might be found.     

Comparison of urease inhibitor N‐(n‐butyl) thiophosphoric triamide and oxidized charcoal for conserving urea‐N in soil

Charcoal‐based amendments have a potential use in controlling NH₃ volatilization from urea fertilization, owing to a high cation‐exchange capacity (CEC) that enhances the retention of NH . An incubation study was conducted to evaluate the potential of oxidized charcoal (OCh) for controlling soil transformations of urea‐N, in comparison to urease inhibition by N‐(n‐butyl) thiophosphoric triamide (NBPT). Four soils, ranging widely in texture and CEC, were incubated aerobically for 0, 1, 3, 7, and 14 d after application of ¹⁵N‐labeled urea with or without OCh (150 g kg^?1 fertilizer) or NBPT (0.5 g kg^?1 fertilizer), and analyses were performed to determine residual urea and ¹⁵N recovery as volatilized NH₃, mineral N (as exchangeable NH , NO , and NO ), and immobilized organic N. The OCh amendment reduced NH₃ volatilization by up to 12% but had no effect on urea hydrolysis, NH and NO concentrations, NO accumulation, or immobilization. In contrast, the use of NBPT to inhibit urea hydrolysis was markedly effective for moderating the accumulation of NH , which reduced immobilization and also controlled NH₃ toxicity to nitrifying microorganisms that otherwise caused the accumulation of NO instead of NO . Oxidized charcoal is not a viable alternative to NBPT for increasing the efficiency of urea fertilization.     

How does the application of different nitrification inhibitors affect nitrous oxide emissions and nitrate leaching from cow urine in grazed pastures?

Nitrous oxide (N₂O) is a potent greenhouse gas, and nitrate () is a water contaminant. In grazed grassland, the major source of both leaching and N₂O emissions is nitrogen (N) deposited in animal excreta, particularly in the urine. The objective of this study was to determine the effectiveness of two nitrification inhibitors: (i) a solution of dicyandiamide (DCD) and (ii) a liquid formulation of 3,4‐dimethylpyrazole phosphate (DMPP) for reducing N₂O emissions and leaching from urine patch areas in two grazed pasture soils under different environmental conditions. In the Canterbury Templeton soil, the nitrification rate of ammonium from the animal urine applied at 1000 kg N/ha was significantly decreased by the application of DCD (10 kg/ha) and DMPP (5 kg/ha). N₂O emissions, measured over a 3‐month period, from dairy cow urine applied to the Canterbury Templeton soil were 1.14 kg N₂O‐N/ha, and this was reduced to 0.43 and 0.39 kg N₂O‐N/ha by DCD and the liquid DMPP, respectively. These are equivalent to 62–66% reductions in the total N₂O emissions. Nitrate leaching losses from dairy cow urine applied to the Waikato Horotiu soil lysimeters were reduced from 628.6 kg ‐N/ha to 400.6 and 451.5 kg ‐N/ha by the application of DCD (10 kg/ha) or DMPP (1 kg/ha), respectively. There was no significant difference between the DCD solution and the liquid DMPP in terms of their effectiveness in reducing N₂O emissions or leaching under the experimental conditions of this study. These results suggest that both the liquid formulations of DCD and DMPP have the potential to be used as nitrification inhibitors to reduce N₂O emissions and leaching in grazed pasture soils.     

Lead sorption to selected Portuguese soils

We studied the interaction of lead with seven Portuguese soils with different physical and chemical properties in order to elucidate more fully the behaviour of Pb in soil. We studied these adsorption phenomena by voltammetric titrations with differential pulse polarography (DPP) at different pH (6.0–7.2) and ionic strengths, I (0.010–0.50 m ) in order to clarify some of the factors that might control soil sorption capacity for Pb. From the voltammetric data, average formation constants, , and binding capacity, C_c, have been estimated according to a surface complexation model based on Scatchard and van den Berg–R?zic methods. Linear Scatchard and van den Berg–R?zic plots (r≥ 0.99) indicated that the results can be interpreted according to the existence of just one predominant active site for Pb(II) adsorption. The values from both procedures () agreed in all cases (r= 0.938, n= 66, P < 0.001). The same happened with C_c values that were statistically equivalent (r= 0.9998; n= 66; P < 0.001). The C_c values were found to depend on the pH and I, as well as on the soil properties. Either Langmuir or Freundlich isotherms fitted the experimental data well (r > 0.90, P < 0.05). The lead binding capacities were strongly and significantly correlated (P < 0.05) with pH, cation exchange capacity, organic carbon, loss‐on‐ignition, total Al₂O₃ content, extractable forms of Al and pyrophosphate extractable Fe, [Fe_p]. From a forward, stepwise regression model we concluded that [Al₂O₃], [Pb′] (concentration of labile lead in solution), [Fe_p], pH and I are able to explain more than 99.7% of the variation in lead sorption in our soils. The soils’ surface groups with special affinity to Pb(II) are in the inorganic fraction associated with aluminium.     

Nitrate stability in loess soils under anaerobic conditions—laboratory studies

The objective of this laboratory study with six loess soils (three Eutric CambisoIs and three Haplic Phaeozems) incubated under flooded conditions was to examine the effect of a wide range of NO doses under anaerobic conditions on soil redox potential and N₂O emission or absorption. Due to the fact that loess soils are usually well‐drained and are expected to be absorbers during prevailing part of the season, the study aimed at determination of the conditions decisive for the transition from emission to absorption process. On the basis of the response to soil nitrate level, the two groups of soils were distinguished with high and low denitrification capacity. The soil denitrification activity showed Michaelis‐Menten kinetics with respect to soil nitrate content with K_M in the range 50–100 mg NO ‐N kg^–1. Percentage of nitrates converted to N₂O increased linearly with nitrate concentration in the range from 25 to 100 mg NO ‐N kg^–1 up to 43% and decreased linearly at higher concentrations reaching practically zero at concentrations about 600 mg NO ‐N kg^–1. No denitrification was observed below 25 mg NO ‐N kg^–1. Nitrous oxide absorption in soil occurred only at nitrate concentrations to 100 mg NO ‐N kg^–1 and in this concentration range was proportional to the denitrification rate. Nitrous oxide was formed at redox potentials below +200 mV and started to disappear at negative E_h values.     

Toxic levels of metals in Ferralsols under natural vegetation and crops in New Caledonia

The chemistry of soil solutions and the potential toxicity of trace metals (Co, Cr, Cu, Ni and Mn) were investigated on soils formed on ultramafic rocks. Soil solutions were collected along a soil toposequence under natural vegetation and under a cropped field. In the latter, metal speciation and species activity were computed with the WHAM 6 model. Total element concentrations varied with the soil topographic position. Upslope, in well‐drained soils, they were relatively small with mean concentrations of <0.2 µmol l⁻¹ for Co and Cr and <2 µmol l⁻¹ for Ni and Mn. Downslope, in temporarily waterlogged soils, concentrations reached 37 (Mn), 5.6 (Ni), 1.9 (Co) and 0.1 (Cr) µmol l⁻¹. Under crops, Ni, Mn and Co concentrations were similar to those under natural vegetation, but Cr concentration averaged 5 µmol l⁻¹. Cu concentration was close to 1 µmol l⁻¹. Free‐ion species amounted to 53–71% of all species for Co, Ni and Mn but only 5% for Cu. Cr was almost entirely in the Cr(VI) form (CrO, HCrO. The free‐metal‐ion activities were in the range 26–81% of the corresponding free‐metal‐ion concentration. Comparing our data with levels that are toxic to crops, Ni and Cr are potentially toxic in the well‐drained and the poorly‐drained soils. In the latter, Co and Mn are also potentially toxic. Both the large concentration of metals and the chemical species in which they occur in solution could limit the use of the land for agricultural purpose.     

Effect of nitrogen forms and levels on β‐glucan accumulation in grains of oat (Avena sativa L.) plants

Oat consumption has been rapidly increased worldwide because its high β‐glucan concentration may lower the level of blood cholesterol. The rates of β‐glucan accumulation in two husk and two nude oats were determined with an interval of 5 d after anthesis in a pot experiment. The results showed that a higher nitrogen level increased oat grain yield per plant, thousand‐grain weight, and concentrations of protein and β‐glucan. β‐glucan concentration generally increased with development of grain after anthesis, whereas the accumulation rate of β‐glucan was greater at the early stage of grain development and reached a maximum around 25 d after anthesis. We also found a larger β‐glucan concentration when plants were grown with NO ‐N as compared to NH ‐N. This study may suggest that the agronomic approaches such as nutrient management by optimizing the time and the level of nitrogen application and a higher ratio of NO ‐N to NH ‐N can play an important role in enhancing β‐glucan concentration in oat grains.     

Effects of the nitrification inhibitor dicyandiamide on soil mineral N, pasture yield, nutrient uptake and pasture quality in a grazed pasture system

Recent lysimeter studies have demonstrated that the nitrification inhibitor, dicyandiamide (DCD), can reduce nitrate (NO) leaching losses from cow urine patches in grazed pasture systems. The objective of this study was to quantify the effects of fine particle suspension (FPS) DCD on soil mineral N components, pasture yield, nutrient uptake and pasture quality under grazed pasture conditions. A field study was conducted on the Lincoln University dairy farm, Canterbury, New Zealand, from 2002 to 2006. FPS DCD was applied to grazed pasture plots at 10 kg ha^?1 in early May in addition to applied cow urine patches at a nitrogen (N) loading rate of 1000 kg N ha^?1, with DCD reapplied in early August. Soil mineral N levels in the urine patches were monitored. Pasture yield, N and cation concentrations and uptake were measured in treatment urine patches and inter‐urine areas of the pasture. Comparisons were made with control plots which did not receive DCD. NO levels under the DCD‐treated urine patches (0–7.5 cm) were in the order of 10 kg N ha^?1 compared with 40–80 kg N ha^?1 under untreated patches, and soil ammonium (NH) levels were consistently higher under the DCD‐treated patches. The DCD significantly and consistently increased pasture yield in both the urine patches, and inter‐urine areas of the pasture in all 4 years of the trial. Mean annual dry matter (DM) yields over 4 years were inter‐urine areas, 10.3; inter‐urine + DCD, 12.4; urine, 12.4 and urine +DCD 16.0 t DM ha^?1, representing an average DM yield increase of 20 and 29% in inter‐urine and urine patch areas, respectively. On a whole paddock basis, the increase in annual DM yield resulting from DCD application was estimated to be 21%. N, calcium (Ca), magnesium (Mg) and potassium (K) concentrations in pasture were unaffected by treatment with DCD; however, total annual uptake of these nutrients by pasture was significantly higher in all years where DCD had been applied. Pasture DM, protein, carbohydrate, metabolizable energy and fibre levels and sward clover content were not affected by treatment with DCD. The results demonstrate the agronomic value of the DCD treatment in addition to the environmental benefits in a grazed pasture system.     

Verteilung von Stickstoff auf Sproß und Wurzel bei jungen Bohnenpflanzen nach der Aufnahme von NO und NH

Translocation of nitrogen to the shoot of young bean plants after uptake of NO and NH by the root Phaseolus vulgaris plants (var. nana, cv. Saxa) at the primary leaf stage (without nodules) were fed during 6 hours with ¹⁵NO and ¹⁵NH, respectively. 24 hours after the absorption period more ₁₅N from the absorbed NO was translocated from the root to the shoot. The presence of NH in the nutrient solution enhanced the translocation of ¹⁵NON, probably by an inhibition of nitrate reductase. NH_4-⁺¹⁵N is mainly retained in the root by a high incorporation into the root protein. It can be concluded that nitrogen from newly absorbed NO is not retained and used for protein synthesis in the root according to the root's potential to synthesize protein. Nitrate reduction in the root is considered to be the limiting factor. This is supported by the fact that withdrawal of NO in the nutrient solution prior to the ¹⁵N-experiment increased NOtranslocation to the shoot as a consequence of a lowered level of nitrate reductase. In an experiment with ¹⁴NOsupply to the roots and ¹⁵NOapplication to the primary leaves (infiltration method) a considerable amount of ¹⁵N was translocated from the leaves to the roots. This indicates that an insufficient NOreduction in the root can be substituted by a retranslocation of reduced N-compounds from leaves to the roots. The proportion of NO reduced in the root influences also the pattern of primary distribution of nitrogen in the shoot of plants at the 4 leaf stage. At a concentration of 0,2 meq/l NO in the nutrient solution as compared to 20 meq/l NO during 10 hours a relative higher amount of ₁₅N was transported from the root to the younger, growing leaves i.e. via the phloem to metabolic sinks.     

THE MECHANICAL STRENGTH OF UNSATURATED POROUS GRANULAR MATERIAL

The influence of pore-water suction on the strength of a porous material is that it contributes a compressive load which increases the shear strength. When the material is unsaturated, the normal load or effective stress is due, in part to the continuous water at measured suction in unemptied pores, and in part to isolated bodies in nominally emptied pores at suctions approximating to the suction at emptying. When the material is draining from saturation, the effective stress σ is where S is the fraction of saturation, α is the fraction of the initial water content drained at the maximum suction, _Ps_d is the prevailing pore water suction, and _Ps_d is a suction passed through in reaching _pS_d at which the reduction of S is dS. When the material is rewetting, the relationship becomes where _ps_w is now the prevailing suction during wetting and f is a distribution function of the degree of saturation such that δS is the fractional saturation removed in the suction range δs_d at s_d and regained in the suction range δs_w at s_w. _ms_d is the maximum suction attained. The effective stress is revealed experimentally by unconfined compression tests on samples with imposed pore water suctions, and the dependence on this suction confirms reasonably that which is predicted by the theoretical formulas.     

Dissolved organic nitrogen and carbon in pastoral soils: the New Zealand experience

Dissolved organic nitrogen (DON) and dissolved organic carbon (DOC) in soils are increasingly recognized as important components of nutrient cycling and biological processes in soil‐plant ecosystems. The aims of this study were to: (i) quantify the pools of DON and DOC in a range of New Zealand pastoral soils; (ii) compare the effects of land use changes on these pools; and (iii) examine the seasonal variability associated with these two components of dissolved organic matter. Soil samples (0–7.5 cm depth) from 93 pastoral sites located in Northland, Waikato, Bay of Plenty and Otago/Southland, New Zealand, were collected in autumn. Adjacent sites under long‐term arable cropping or native vegetation and forestry land use were also sampled at the same time to estimate the impacts of different land use on DON and DOC in these soils. Twelve dairy and 12 sheep and or beef pastures were sampled in winter, spring, summer and autumn for a 2‐year period to study the seasonal fluctuations of DON and DOC. A field incubation study was also carried out in a grazed pasture to examine fluctuations in the concentrations of and and DON levels in soil. Other soil biological properties, such as microbial biomass‐C, biomass‐N and mineralizable N, were also measured. Pastoral soils contained the greatest amounts of DON (13–93 mg N kg⁻¹ soil, equivalent to 8–55 kg N ha⁻¹) and DOC (73–718 mg C kg⁻¹ soil, equivalent to 44–431 kg C ha⁻¹), followed by cropping and native vegetation and forestry soils. The DON concentration in soils was found to be more seasonally variable than DOC. There was approximately 80% fluctuation in the concentration of DON in winter from the annual mean concentration of DON, while DOC fluctuated between 23 and 28% at the dairy and the sheep and beef monitoring sites. Similar fluctuations in the concentrations of DON were also observed in the field incubation studies. These results indicate that DON is a dynamic pool of N in soils. There was a strong and significant positive correlation between DON and DOC in pastoral soils (r = 0.71, P < 0.01). There were also significant positive correlations between DON and total soil C (r = 0.59, P < 0.01), total soil N (r = 0.62, P < 0.01) and mineralizable N (r = 0.47, P < 0.01). The rather poor correlations between total soil C and N with DOC and DON, suggest other biogeochemical processes may be influencing concentrations of DOC and DON in these soils. Given the size of DON and DOC pools in the pastoral soils, we suggest that these pools of C and N should be taken into account when assessing the impact of pastoral land use on soil C and N enrichment of surface and groundwater.     

Effects of rainfall pattern on carbon and nitrogen dynamics in soil amended with biogas slurry and composted cattle manure

Soil moisture affects the degradation of organic fertilizers in soils considerably, but less is known about the importance of rainfall pattern on the turnover of C and N. The objective of this study was to determine the effects of different rainfall patterns on C and N dynamics in soil amended with either biogas slurry (BS) or composted cattle manure (CM). Undisturbed soil cores without (control) or with BS or CM, which were incorporated at a rate of 100 kg N ha^–1, were incubated for 140 d at 13.5°C. Irrigation treatments were (1) continuous irrigation (cont_irr; 3 mm d^–1); (2) partial drying and stronger irrigation (part_dry; no irrigation for 3 weeks, 1 week with 13.5 mm d^–1), and (3) periodic heavy rainfall (hvy_rain; 24 mm d^–1 every 3 weeks for 1 d and 2 mm d^–1 for the other days). The average irrigation was 3 mm d^–1 in each treatment. Cumulative emissions of CO₂ and N₂O from soils amended with BS were 92.8 g CO₂‐C m^–2 and 162.4 mg N₂O‐N m^–2, respectively, whereas emissions from soils amended with CM were 87.8 g CO₂‐C m^–2 and only 38.9 mg N₂O‐N m^–2. While both organic fertilizers significantly increased CO₂ production compared to the control, N₂O emissions were only significantly increased in the BS‐amended soil. Under the conditions of the experiment, the rainfall pattern affected the temporal production of CO₂ and N₂O, but not the cumulative emissions. Cumulative NO leaching was highest in the BS‐amended soils (9.2 g NO ‐N m^–2) followed by the CM‐amended soil (6.1 g NO ‐N m^–2) and lowest in the control (4.7 g NO ‐N m^–2). Nitrate leaching was also independent of the rainfall pattern. Our study shows that rainfall pattern may not affect CO₂ and N₂O emissions and NO leaching markedly provided that the soil does not completely dry out.     

THE MEASUREMENT AND MECHANISM OF ION DIFFUSION IN SOIL

If an exchangeable ion in soil diffuses along a liquid and solid pathway, its diffusion coefficient may be expressed as where D, v, f, C are diffusion coefficient, volume fraction, impedance factor, and concentration terms and the suffixes _l,_S refer to liquid and solid. The self-diffusion coefficient of the ion is then where D′, D′_t, and D′_s, are self-diffusion coefficients. D and D′ will vary with concentration. In diffusion out of the soil to a zero sink, the appropriate average diffusion coefficient is, approximately, the self-diffusion coefficient in the undisturbed soil. Diffusion of one ion species is influenced by other ions diffusing in the system through the diffusion potential set up. When ions are diffusing to plant roots, the diffusion potential is likely to be small. A more likely, though more complicated, expression for D than the first equation above is derived by assuming the ion to follow solid and liquid pathways in series as well as in parallel.     

Plant availability and leaching of (heavy) metals from ammonium‐, calcium‐, carbohydrate‐, and citric acid‐treated uranium‐mine‐dump soil

Remediation of an uranium‐mine soil from Settendorf (East Germany) includes phytoextraction under conditions which make its heavy metals more plant‐available but less leachable. A second way is active inhibition of heavy metal uptake by the plant. In a pot trial with Chinese cabbage (Brassica chinensis L.), planted and unplanted soil samples were daily irrigated with deionized water or aqueous solutions with a total of (g (kg soil)^–1) CaCl₂ (0.26 Ca), NH₄Cl (1.39), casein, sucrose, citric acid (13), and an extract of rape (B. napus L.) shoots (13 DW) in a phytotron for 26 d. Water‐irrigated plants were also treated with a 50 mM citric acid solution (10.5 g (kg soil)^–1) 6 and 7 d prior to harvesting. Total elements in plant tissue and soluble elements in aqueous extracts from control and postharvest soils were determined by ICP‐AES. Supplements of NH , and the NH ‐generating casein and rape extract reduced soil pH during nitrification, and increased plant uptake of Cd, Cu, Ni, and Zn. Citric acid at 50 mM adjusted soil to pH 4.5–6.0 and enhanced uptake of all elements. Long‐term application of sucrose and citric acid increased pH and inhibited uptake of Cd, Cr, Cu, Ni, and Zn. Contemporarily, leaching of heavy metals and humic substances was lowest with Ca and NH and highest with sucrose and citric acid amendments. It is concluded that Chinese cabbage grown for chelate‐assisted phytoextraction should be supplied with Ca and NH to obtain a high plant biomass on soil with a low hazard of leaching. Metal uptake should be stimulated by application of chelator 7 d prior to harvesting. Undesired uptake of heavy metals by Chinese cabbage determined as food should be inhibited with carbohydrate amendments. Long‐term application of NH or chelator, which reduces the solubility of certain elements but increases their uptake moderately, is recommended as a tool for continuous phytoextraction technologies.     

Nitrogen fertilization and nitrate leaching into groundwater on arable sandy soils

Nitrate leaching depending on N fertilization and different crop rotations was studied at two sites with sandy soils in N Germany between 1995 and 2000. The leaching of NO was calculated by using a numerical soil‐water and N model and regularly measured N_min values as input data. Also the variability of N_min values on the sandy soils was determined along transects. They reveal the high variability of the N_min values and show that it is not possible to confirm a significant N_min difference between fertilizer treatments using the normal N_min‐sampling intensity. Nitrate‐leaching calculations of five leaching periods showed that even strongly reduced N‐fertilizer applications did not result in a substantially lower NO leaching into the groundwater. Strong yield reductions of even more than 50%, however, were immediately measured. Mean NO concentrations in the groundwater recharge are >50 mg L^–1 and are mainly due to mineralization from soil organic matter. Obviously, the adjustment of the N cycle in the soil to a new equilibrium and a reduced NO ‐leaching rate as a consequence of lower N inputs need a much longer time span. Catch crops are the most efficient way to reduce the NO concentrations in the groundwater recharge of sandy soils. Their success, however, strongly depends on the site‐specific development possibilities of the catch crop. Even with all possible measures implemented, it will be almost impossible to reach NO concentrations <50 mg L^–1 in sandy soils. The only way to realize this goal on a regional scale could be by increasing areas with lower nitrate concentrations in the groundwater recharge like grassland and forests.     

Impact of urease and nitrification inhibitor on NH4+ and NO3− dynamic in soil after urea spring application under field conditions evaluated by soil extraction and soil solution sampling

The application of mineral nitrogen (N) fertilizers is one of the most important management tools to ensure and increase yield in agricultural systems. However, N fertilization can lead to various ecological problems such as nitrate () leaching or ammonia and nitrous oxide emissions. The application of N stabilizers (i.e., inhibitors) combined with urea fertilization offers an effective option to reduce or even prevent N losses due to their regulatory effect on ammonium () and release into the soil. The present field experiment therefore aimed at soil N speciation dynamics after urea spring fertilization (225 kg N ha^?1) in the presence of a urease inhibitor (UI), a nitrification inhibitor (NI), both inhibitors (UI+NI) or when no inhibitor was applied at all. The study focused on the distribution of N species among soil matrix and soil solution. Plant cultivation was completely omitted in order to avoid masking soil N turnover and speciation by plant N uptake and growth dynamics. Application of UI clearly delayed urea hydrolysis in the top soil, but a complete hydrolysis of urea took place within only 10 days after fertilization (DAF). Nitrification was significantly reduced by NI application, leading to higher and lower concentrations in treatments with NI. Due to sorption of to the soil matrix a significantly larger fraction of was always detected in the soil extracts compared to soil solution. However, while in soil extracts the impact of NI application was less apparent and delayed, in soil solution a quick response to NI application was observed as revealed by significantly increased soil solution concentrations of . Because of the “asymmetric” soil phase distribution soil solution was predominant over only initially after fertilization even in inhibitor treatments (≈ 8 to 10 DAF). Nevertheless, inhibitor application tended towards closer ratios of to concentration in soil solution and hence, might additionally affect concentration dependent processes like plant N uptake and root development. Despite cold spring conditions urea application along with UI and/or NI did not indicate a limited supply of plant available and .