An Exploratory Investigation on the Mobility of Polybrominated Diphenyl Ethers (PBDEs) in Biosolid-Amended Soil

Polybrominated diphenyl ethers (PBDEs) have been found at high levels, up to 7.6?×?10⁶?pg/g, in biosolids commonly applied to agricultural soils. A field investigation was carried out in this study to measure concentrations of PBDEs in biosolid-amended agricultural soils in which various amounts of biosolids (20 and 80?t/ha) had been applied. Concentrations of PBDEs in surface soils that had received a single application of 80?t/ha biosolids were one to two orders of magnitude greater than that in soil, which had received a single application of 20?t/ha of biosolids. Assessment of PBDEs levels at different depths, between 0.05 and 1.05?m, in soils that received 80?t/ha biosolids, showed that PBDEs were mobilized from the surface soil to lower depths. Total PBDEs concentrations decreased from 10,250?pg/g dry weight basis (dw) in the 0.05?m soil layer to 220?pg/g dw at a depth of 1?m. The distribution of PBDEs with depth and cation exchange capacity of the soil could be described as exponential functions. The coefficients of correlation ranged from 0.47 to 0.57 and 0.47 to 0.67, respectively. Despite the deviation in the experimental measurements induced by variables, such as non-uniform biosolid application, heterogeneity of the soil, and the uneven surface of the field, variations of PBDEs along the soil profile in the biosolid-amended soil were clearly demonstrated.     

Partitioning of Hg Between Solid and Dissolved Organic Matter in the Humus Layer of Boreal Forests

The mobility of mercury (Hg) deposited on soils controls the concentration and toxicity of Hg within soils and in nearby streams and lakes, but has rarely been quantified under field conditions. We studied the in situ partitioning of Hg in the organic top layer (mor) of podsols at two boreal forest sites differing in Hg deposition and climatic regime (S. and N. Sweden, with pollution declining to the north). Soil solution leaching from the mor layer was repeatedly sampled using zero-tension lysimeters over 2 years, partly in parallel with tension lysimeters. Concentrations of Hg and dissolved organic carbon (DOC) were higher while pH was lower at the southern site (means ± SD: Hg?=?44?±?15 ng L^?1, DOC?=?63.0?±?31.3 mg L^?1, pH?=?4.05?±?0.53) than at the northern site (Hg?=?22?±?6 ng L^?1, DOC?=?41.8?±?12.1 mg L^?1, pH?=?4.28?±?0.43). There was a positive correlation over time between dissolved Hg and DOC at both sites, even though the DOC concentration peaked during autumn at both sites, while the Hg concentration remained more constant. This correlation is consistent with the expected strong association of Hg with organic matter and supports the use of Hg/C ratios in assessments of Hg mobility. In the solid phase of the overlying O_f layer, both Hg concentrations and Hg/C ratios were higher at the southern site (means ± SD: 0.34?±?0.06 μg g^?1 dw and 0.76?±?0.14 μg g^?1 C, respectively) than at the northern site (0.31?±?0.05 μg g^?1 dw and 0.70?±?0.12 μg g^?1 C, respectively). However, concentrations in the solid phase differed less than might be expected from the difference in current atmospheric input, suggesting that the fraction of natural Hg is still substantial. At both sites, Hg/C ratios in the upper half of the mor layer were only about two thirds of those in the lower half, suggesting that the recent decrease in anthropogenic Hg deposition onto the soil is offset by a natural downward enrichment of Hg due to soil decomposition or other processes. Most interestingly, comparison with soil leachate showed that the average Hg/C ratios in the dissolved phase of the mor layers at both sites did not differ from the average Hg/C ratios in the overlying solid organic matter. These results indicate a simple mobilisation with negligible fractionation, despite differences in Hg deposition patterns, soil chemistry and climatic regimes. Such a straight-forward linkage between Hg and organic matter greatly facilitates the parameterisation of watershed models for assessing the biogeochemical fate, toxic effect and critical level of atmospheric Hg input to forest soils.     

Major nutrients,heavy metals and PBDEs in soils after long-term sewage sludge application

Purpose

Two contrasting soils receiving long-term application of commercial sewage sludge fertilizers in China were investigated to determine the concentrations of selected nutrients, heavy metals (HMs) and polybrominated diphenyl ethers (PBDEs) present to evaluate the impact of sewage sludge fertilizer on soil fertility and environmental risk.

Materials and methods

Soil samples were collected from Tangshan City, Hebei province and Ningbo City, Zhejiang province and divided into two portions, one of which was air-dried and sieved through 2-, 0.25- and 0.149-mm nylon mesh for determination of nutrients and heavy metals. The other portion was frozen at ?20°C, freeze-dried and sieved through 2-mm nylon mesh for PBDE analysis. The concentrations of nutrients, heavy metals and PBDEs were determined in all samples.

Results and discussion

Concentrations of nutrients and heavy metals in soils amended with low rates of sewage sludge fertilizer (SSF) and conventional fertilizer were compared. After long-term excessive amendment with SSF from Ningbo City (SSF-N), the concentrations of soil total N, P, aqua regia-extractable HMs and DTPA extractable HMs were higher than the control, especially in the arable layer. Moreover, the concentration of aqua regia-extractable Zn (457 mg kg^?1) exceeded the recommended China Environmental Quality Standard for soils (GB15618-1995). All 8 target PBDE congeners were found in fertilizer SSF-N and soil with excessive amendment with SSF-N for 12 years, but the concentrations of 8 different PBDEs in SSF-N-amended soil were not significantly different from control soil.

Conclusions

Both economic and environmental benefits can be obtained by careful application of sewage sludge fertilizer to recycle plant nutrients. Repeated and excessive application rates of sewage sludge fertilizer may pose environmental risk, especially in respect of soil heavy metal and PBDE contamination, and high concentrations of phosphorus may also be environmentally detrimental.

     

Clay Addition to Sandy Soil Reduces Nutrient Leaching—Effect of Clay Concentration and Ped Size

Leaching of nutrients, particularly in sandy soil with low nutrient and water holding capacity (WHC), is a major threat to marine and fresh water pollution. Addition of clay soil to sandy soil could be an option to increase water and nutrient holding capacity of sandy soils, but the effect of clay soil addition may depend on the form in which the clay soil is added and the addition rate. Clay soil was added to sandy soil at rate of 10 or 20% (w/w) finely ground (<2 mm) or 2 and 5 mm peds with and without nitrogen (N) and phosphorus (P) fertilizer equivalent to 60 kg N ha^?1 and 15 kg P ha^?1. The clay sand mixture for each treatment was weighed (30 g) in cores with nylon mesh at the bottom. The soils were incubated at 80% WHC for 7 weeks. To obtain leachate, 20 mL reverse osmosis (RO) water was added every week to each core. Leachate was analysed for inorganic N, P, and pH. Soil was analyzed for N, P, and pH before and after the leaching. Clay addition significantly reduced the leaching of N and P compared to sandy soil alone, with greatest reduction by finely ground clay soil and least with 5 mm peds. Compared to sandy soil alone, 83% more N was retained in clay-amended soil and P retention was doubled. This study showed that addition of finely ground clay soil can substantially reduce N and P leaching and thereby increase fertilizer retention compared to sandy soil alone.     

Polybrominated Diphenyl Ether Leachability from Biosolids and Their Partitioning Characteristics in the Leachate

Biosolids are commonly applied to agricultural soils. A laboratory investigation was carried out to determine polybrominated diphenyl ether (PBDE) congener profiles in biosolids and leachability by water. In addition, PBDE fractionation in water and suspended solids of different sizes was examined to determine the potential for enhanced mobility of these contaminants within soils. The leachates from glass column experiments were passed through a series of filters, and the filtrates and retained particles analyzed for PBDEs. PBDEs were found to sorb on solid particles suspended in the leachate, allowing PBDEs to be present at concentrations exceeding their aqueous solubilities. The filtration process indicated that PBDEs are associated with fine and ultrafine particles. Filters of different pore sizes provide a better indication of PBDE levels in the leachate compared to not filtering or using a single filter. PBDEs concentrations were much higher on ultrafine than on fine particles, due to the greater surface area and higher organic content of the former.     

Pilot-scale counter-current acid leaching process for Cu,Pb, Sb,and Zn from small-arms shooting range soil

Purpose

The main objective of this study was to evaluate the potential of a counter-current leaching process (CCLP) on 14 cycles with leachate treatment at the pilot scale for Pb, Cu, Sb, and Zn removal from the soil of a Canadian small-arms shooting range.

Materials and methods

The metal concentrations in the contaminated soil were 904?±?112 mg Cu kg^–1, 8,550?±?940 mg Pb kg^–1, 370?±?26 mg Sb kg^–1, and 169?±?14 mg Zn kg^–1. The CCLP includes three acid leaching steps (0.125 M H₂SO₄?+?4 M NaCl, pulp density (PD)?=?10 %, t?=?1 h, T?=?20 °C, total volume?=?20 L). The leachate treatment was performed using metal precipitation with a 5-M NaOH solution. The treated effluent was reused for the next metal leaching steps.

Results and discussion

The average metal removal yields were 80.9?±?2.3 % of Cu, 94.5?±?0.7 % of Pb, 51.1?±?4.8 % of Sb, and 43.9?±?3.9 % of Zn. Compared to a conventional leaching process, the CCLP allows a significant economy of water (24,500 L water per ton of soil), sulfuric acid (133 L H₂SO₄ t^–1), NaCl (6,310 kg NaCl t^–1), and NaOH (225 kg NaOH t^–1). This corresponds to 82 %, 65 %, 90 %, and 75 % of reduction, respectively. The Toxicity Characteristic Leaching Procedure test, which was applied on the remediated soil, demonstrated a large decrease of the lead availability (0.8 mg Pb L^–1) in comparison to the untreated soil (142 mg Pb L^–1). The estimated total cost of this soil remediation process is 267 US$ t^–1.

Conclusions

The CCLP process allows high removal yields for Pb and Cu and a significant reduction in water and chemical consumption. Further work should examine the extraction of Sb from small-arms shooting range.     

EDTA Leaching of Cu Contaminated Soils Using Ozone/UV for Treatment and Reuse of Washing Solution in a Closed Loop

Ozone and UV irradiation were used for oxidative decomposition of EDTA-Cu complexes in washing solution obtained during multi-step leaching of Cu (344,1?±?36.5 mg kg^?1) contaminated vineyard soil with EDTA as a chelant. The released Cu was absorbed from the washing solution on a commercial mixture of metal absorbing minerals, and the treated washing solution then reused for removal of soil residual Cu-EDTA complexes in a closed-loop process. Six consecutive leaching steps (6?×?2.5 mmol kg^?1 of EDTA) removed 38.8 % of Cu from soils, and reduced Cu soil mobility, determined using the toxicity characteristic leaching test (TCLP), by 28.5%. The final washing solution obtained after soil remediation was colourless, with a pH close to neutral (7.5?±?0.2) and with low concentrations of Cu and EDTA (0.51?±?0.22 mg L^?1 and 0.083 mM, respectively). The proposed remediation method has therefore potential not just to recycle and save process water, but also not to produce toxic wastewaters. Soil treatment did not substantially alter the soil properties determined by pedological analysis, and had relatively little impact on soil hydraulic conductivity and soil water sorption capacity.     

Effect of two moisture regimes on P-release from P treated soils

Understanding phosphorus (P) release under different climatic or moisture regimes will facilitate effective management of plant nutrition. The objective of this study is to evaluate the effect of two soil moisture regimes on P release from Ogun rock phosphate (ORP) and Sokoto rock phosphate (SRP) in two soil types. Soil was poured into soil columns to form lower and top layers. Top layer was mixed with 400 kg ha^?1 P from ORP, SRP, single super phosphate (SSP) and leached with 35.4 cm³ water representing low moisture regime (LMR; 400 mm rainfall) and 106.1 cm³ water for high moisture regime (HMR; 1200 mm rainfall). P concentrations of leachates, available P in soil and soil pH were determined. Cumulative P leached was higher under HMR than LMR in both soils. There was more leaching with SSP (0.41–0.97 mg P) than both phosphate rocks (0.008–0.19 mg P) indicating leaching potential of SSP. Cumulative P leached from SSP treated Olokemeji soils was twice that of acidic Sapoba under LMR while they were similar (Olokemeji, 0.97 mg P; Sapoba, 0.94 mg P) under HMR suggesting that LMR enhances fixation of P in acidic soils. Irrigation of P fertilized soils may reduce P sorption in acidic soils.     

Effects of rainfall and manure application on phosphorus leaching in field lysimeters during fallow season

Purpose

Transformation and transport of soil phosphorus (P) from chemical fertilizer or manure are affected by agronomic practices (i.e., fertilization, irrigation, and tillage) and numerous abiotic factors (i.e., temperature, drought, and rainfall). Previous studies on the effects of manure application on P loss were mostly conducted during cultivation and often using the laboratory column approach. Validated field observations by integrating P availability with the risk of P loss are few. This study aimed to evaluate the effects of rainfall and manure application on P leaching during fallow season.

Materials and methods

An in situ field lysimeter experiment was performed. Leachate was collected and analyzed for total P (TP) and dissolved reactive P (DRP). At the end of the lysimeter trial, soils were sampled incrementally to a depth of 40 cm with the following depth intervals: 0–4, 4–10, 10–20, 20–30, and 30–40 cm. Soil water extractable P (P_w) was analyzed and degree of P saturation (DPS) was calculated after oxalate and Mehlich-3 (M3) extractions.

Results and discussion

Phosphorus loading was found below 40 cm in all treatments and P was most concentrated in the 4–10 cm soil layer. High rainfall enhanced P leaching and consequently led to lower P_w and higher leachate DRP and TP than low rainfall. Furthermore, P leaching was observed regardless of manure application, with the highest leachate DRP (1.83 mg L^?1) and TP (7.46 mg L^?1) concentrations found at the end of experiment (day 53). Observed P leaching loads during fallow season (53 days) varied between 0.08 and 1.21 kg ha^?1. The thresholds of DPS indicating P leaching were identified at 18.9% DPS_M3(Ca) and 12.9% DPS_M3(Ca+Mg), respectively. In this study, the DPS_M3(Ca) and DPS_M3(Ca+Mg) values exceeded the corresponding thresholds in the upper 30-cm soil layer but did not reach the thresholds at 30–40 cm. Nevertheless, the leachate DRP and TP indicated soil P leaching.

Conclusions

The results showed that intensive rainfall could significantly increase P leaching from manure application. Moreover, P leaching could occur in fallow season even in the absence of manure input, which should be assessed by not only soil P sorption capacities, but also soil fertilization history and hydrologic conditions. Implementation of soil P level evaluation is critical before spreading manure on land to avoid P pollution. Cost-effective and applicable soil test methods are required to generate environmental indicators to classify agricultural lands for risk of P loss, providing basis to safe manure disposal.     

Downward Movement of Soil Cations in Highly Weathered Soils Caused by Addition of Gypsum

Abstract

Besides supplying calcium (Ca) and sulfur (S) to plants, gypsum has recently been used in agriculture to ameliorate some soil physical and chemical properties, especially to alleviate aluminum phytotoxicity in subsoils. When applied in large quantities, however, gypsum may leach significant amounts of nutrients from the plow layer. This study was conducted to assess the effect of gypsum addition to the soil on the magnitude of cation leaching as well as the relationship of leaching with some soil properties in a group of seven Brazilian soils. Rates of gypsum equivalents to 0, 5.0, 10, and 20 t ha^?1 (0, 2.5, 5.0, and 10 g kg^?1) were mixed with triplicate soil samples consisting of 3.0 kg of dry base soil. After 60 days of incubation at room temperature (15–25°C), the experimental units were packed into polyvinyl chloride leaching columns (32‐cm‐high×10 -cm-diameter) at a density of 0.9 g cm^?3. Thereafter, they were percolated once a week with a volume of distilled water equivalent to 1.5 times the total soil porosity over 11 weeks. Soil samples were collected before the first and after the last percolation, for chemical analysis. Averaged across soils, 11 percolation events leached about 26% of each Ca, magnesium (Mg), and potassium (K) from the treatment without gypsum. Averaged across soils and rates, addition of gypsum leached 41–94% of added Ca, 13–90% of exchangeable Mg, and 13–58% of exchangeable K, and the highest losses occurred on the sandiest soils. The relationship between soil parameters and Ca leaching varied with gypsum rate: in the treatments that received gypsum, leaching was negatively related to cation exchange capacity (CEC), clay, and organic matter, and positively correlated with sand; in the treatment with no gypsum, leaching correlated with the same parameters above, nevertheless, all coefficients presented opposite signs. Leaching of K caused by gypsum was negatively associated with clay and positively with sand, whereas leaching of Mg was poorly correlated with any soil parameter. Gypsum is a good source to promote high and fast downward movement of Ca in the soil profile, but rates must be cautiously chosen because of excessive leaching of Mg especially on soils with low CEC.     

Bacterial numbers and biomass in leachate and in subsoil of a submerged paddy field

By a leaching experiment with glass columns packed with submerged paddy soils, the relationships among numbers of total bacteria, total Gram-positive bacteria, culturare aerobic bacteria and a amount of bacterial biomass both in the leachate, and in the subsoil after leaching incubation were studied. The leachate from soil columns was collected every 3 d during the 30-d incubation period. The soil columns were packed with plow layer soil samples with and without rice straw (RS) amendment, and the subsoil column was connected to the plow layer soil column without RS. Numbers of total bacteria, culturable aerobic bacteria, and a amount of bacterial biomass in the leachate decreased with the incubation time. There was no correlation between the number of total bacteria in the leachate and the concentration of total organic carbon in the leachate. Bacteria less than 0.1 µsm³ in size predominated in the leachate, especially in that from the plow layer soil column with RS. Percentages of the number of Gram-positive bacteria in the leachate were very low (less than 7% of the total bacterial number), while the percentage in the subsoil after the leaching experiment was in the range of 21–82%. The sum of the number of bacteria percolated from the plow layer soil column with RS during the 30-d period of incubation and the sum of the amount of biomass C were 39 and 77% less than the corresponding values for the bacteria percolated from the plow layer soil column without RS. Percentages of culturable aerobic bacteria among the total bacteria ranged between 2.8 and 37% in the leachate, while less than 0.6% in the subsoil after the leaching experiment.     

Sulfonamides Leach from Sandy Loam Soils Under Common Agricultural Practice

Sulfonamide antibiotics can enter agricultural soils by fertilisation with contaminated manure. While only rough estimations on the extent of such applications exist, this pathway results in trace level contamination of groundwater. Therefore, we studied the transport of three sulfonamides in leachates from field lysimeters after application of a sulfonamide-contaminated liquid manure. In a 3-year period, the sulfonamides were determined in 64% to 70% of all leachate samples at concentrations between 0.08 to 56.7 µg L^?1. Furthermore, sulfonamides were determined in leachates up to 23 months after application, which indicated a medium- to long-term leaching risk. Extreme dry weather conditions resulted in highest dislocated amounts of sulfonamides in two of the three treatments. Furthermore, soil management such as tillage and cropping affected the time between application and breakthrough of sulfonamides and the intra-annual distribution of sulfonamide loads in leachates. Although the total sulfonamide leaching loads were low, the concentrations exceeded the limit value of the European Commission of 0.1 µg biocide L^?1 in drinking water in more than 50% of all samples. Furthermore, the medium-term mean concentration of the sulfonamides ranged from 0.08 and 4.00 µg L^?1, which was above the limit value of the European Commission in 91 out of 158 samples. Therefore, sulfonamides applied to soils in liquid manure under common agricultural practice may cause environmental and health risks which call for a setting up of more long-term studies on the fate of antibiotics.     

Reclamation of Alkali Soils: Influence of Amendments and Leaching on Transformation and Availability of Phosphorus

Abstract

Phosphorus (P) availability to plants in reclaimed alkali soils was the main objective of this study, which was also focused on P transformations, decrease in Olsen‐P content, and magnitude of P lost in leachate in course of amendment application and leaching. Liquid sodium bicarbonate (NaHCO₃) was added to nonalkali soils to set up four ESP (exchangeable sodium percentage) levels (viz., 2.9, 25.0, 50.0, and 75.0), but actual ESP levels obtained were 2.9, 24.6, 51.2, and 75.3. Amendments (viz., gypsum and pyrites) and P treatments (viz., 0 and 50 mg P Kg^?1) were mixed with dry, sieved soil before filling into PVC (polyvinyl chloride) drainage columns, which were then compacted to uniform bulk density and leached with deionized water for 30 days. Results indicated that the pH and electrical conductivity (EC) of the soils increased with increase in ESP level of the soil but decreased with amendment application. Phosphorus addition to alkali soils decreased the pH on day 30, but it could not affect the EC of the soils. Successive increase in the ESP level of the soil increased the pH and EC off the leachate. Gypsum‐amended soils exhibited lower pH and EC values than pyrite‐amended soils. The EC of the leachate decreased sharply with time in amended soils, but the pH decreased slowly. Phosphorus addition affected the leachate pH earlier than the soil pH. Cumulative volume of leachate decreased with increasing ESP levels, but it increased with amendment and phosphorus application. Leaching of P increased with increase in ESP levels, and the maximum cumulative loss of P was 11.2 mg Kg^?1 in the 75.3 ESP soil. Cumulative P lost in the pyrite‐amended soils was higher than the gypsum‐amended soils. Phosphorus leaching in the gypsum‐amended soils stopped at day 10 and beyond, but it continued until day 30 in the pyrite‐amended soils. Part of the applied P in alkali soils was also lost along with the native P, whereas it was protected in the nonalkali soils. OlsenP increased with increasing ESP levels, and alkali soils invariably contained higher Olsen P than nonalkali soils. At day 30, alkali soils contained much higher Olsen P (12.6 mg Kg^?1) than nonalkali soils (5.9 mg Kg^?1). In general, there was a decrease in the Olsen P with both of the amendments, but it decreased more with pyrites than with gypsum. Phosphorus added through monopotassium phosphate (KH₂PO₄) remained extractable by Olsen's extractant up to day 30. Results also indicated that percent distribution of ammonium chloride (NH₄Cl)‐P, calcium (Ca)‐P, and unknown P increased with rising ESP levels but iron (Fe)‐aluminum (Al)‐bound P and residual P decreased. Percent distribution of Ca‐P and unknown P exhibited an increase with time also. Unamended alkali soils contained more NH₄Cl‐P than amended ones. Iron and Al‐ bound P and residual P increased more with pyrites, whereas formation of Ca‐P and unknown P was enhanced with gypsum. Applied P tended to convert more into NH₄Cl‐P, Ca‐P, and residual P than to Fe‐Al‐bound P or unknown P fractions. Models developed to estimate Olsen P and P concentration in leachate, through pH or EC, have application value for P management in alkali soils that are leached after application of amendments.     

Integrated Flow-based System Displaying an In-line Mini Soil Column to Monitor Iron Species in Soils Leachates

ABSTRACT

Contamination of ground water as a consequence of soil leaching processes is an issue of major concern. In this context, a simulation of the soil leaching process was designed. A sequential injection (SI) method to monitor the soil leaching of iron complexes with in-line rain simulation for leachate production is described. The developed methodology comprises the SI determination of both iron(III) and 3-hydroxy-4-pyridinones iron(III) complexes, coupled to a mini soil column (mSC) for displaying in-line rain simulations. The described SI method enabled iron(III) determination within the range 2.0–35 µmol L^?1, with a detection limit of 0.42 µmol L^?1, and determination of iron(III) complexes in the range 1.0–45 µmol L^?1. It was successfully applied to leachates from laboratory scale soil columns (LSSC), with good precision for both iron(III) and iron complexes determinations: calculated relative standard deviation (RSD) of 5% and 6%, respectively. A step further in automation and miniaturization was attained with the incorporation of a mini soil column for the in-line leachate production. The system enabled the soil leachate production and assessment in less than 5 min, including determinations in triplicate.     

Relationship between Metals Leached and Soil Type from Potential Acid Sulphate Soils under Acidic and Neutral Conditions in Western Australia

Metal contaminants are likely to be mobilised from soil when in contact with acidic drainage. Soils containing sulphide are often associated with significant quantities of trace metals. Understanding the source of metal pollution is of significant concern for management because sulphide-containing soils are found in close proximity to estuaries, lowland rivers and lakes. This study focuses on Western Australian soils, which are typically sandy and well weathered. Two leachate trials, a batch and a column method, investigated the possibility of characteristic leachate signatures with respect to future traceability of metal contamination from soil drainage. Leaching signatures were assessed for four soil types (grey sand (GS), iron-rich sand (FeRS), silty sand (SS) and peat) found coastally between Perth and Albany, in Western Australia. Trace metals leached from the four soil types showed significant differences for both the metals leached and the concentrations for the column leaching trial. No nickel (<1.0 µgL^?1) but relatively high concentrations of arsenic were leached from the peat site. The FeRS leachates contained chromium, copper, high aluminium and relatively high iron. The GS leached extremely high iron and relatively high manganese concentrations. In comparison, only small concentrations of nickel, iron, aluminium, arsenic and manganese leached from the SS columns. Selenium did not leach above reporting limits (<1.0 µg L^?1) from any of the soil types. This work suggests that leachate signatures from different soil types exist and that soil type should be considered when determining the risk of aquatic impact associated with acidic drainage.     

Effect of 7-year application of a nitrification inhibitor, dicyandiamide (DCD), on soil microbial biomass, protease and deaminase activities, and the abundance of bacteria and archaea in pasture soils

Purpose

The nitrification inhibitor dicyandiamide (DCD) has been shown to be highly effective in reducing nitrate (NO₃ ^?) leaching and nitrous oxide (N₂O) emissions when used to treat grazed pasture soils. However, there have been few studies on the possible effects of long-term DCD use on other soil enzyme activities or the abundance of the general soil microbial communities. The objective of this study was to determine possible effects of long-term DCD use on key soil enzyme activities involved in the nitrogen (N) cycle and the abundance of bacteria and archaea in grazed pasture soils.

Materials and methods

Three field sites used for this study had been treated with DCD for 7 years in field plot experiments. The three pasture soils from three different regions across New Zealand were Pukemutu silt loam in Southland in the southern South Island, Horotiu silt loam in the Waikato in the central North Island and Templeton silt loam in Canterbury in the central South Island. Control and DCD-treated plots were sampled to analyse soil pH, microbial biomass C and N, protease and deaminase activity, and the abundance of bacteria and archaea.

Results and discussion

The three soils varied significantly in the microbial biomass C (858 to 542 μg C g^?1 soil) and biomass N (63 to 28 μg N g^?1), protease (361 to 694 μg tyrosine g^?1 soil h^?1) and deaminase (4.3 to 5.6 μg NH₄ ⁺ g^?1 soil h^?1) activity, and bacteria (bacterial 16S rRNA gene copy number: 1.64?×?10⁹ to 2.77?×?10⁹ g^?1 soil) and archaea (archaeal 16S rRNA gene copy number: 2.67?×?10⁷ to 3.01?×?10⁸ g^?1 soil) abundance. However, 7 years of DCD use did not significantly affect these microbial population abundance and enzymatic activities. Soil pH values were also not significantly affected by the long-term DCD use.

Conclusions

These results support the hypothesis that DCD is a specific enzyme inhibitor for ammonia oxidation and does not affect other non-target microbial and enzyme activities. The DCD nitrification inhibitor technology, therefore, appears to be an effective mitigation technology for nitrate leaching and nitrous oxide emissions in grazed pasture soils with no adverse impacts on the abundance of bacteria and archaea and key enzyme activities.     

Evaluation of Biochar Effects on Nitrogen Retention and Leaching in Multi-Layered Soil Columns

Biochar can play a key role in nutrient cycling, potentially affecting nitrogen retention when applied to soils. In this project, laboratory experiments were conducted to investigate the adsorption properties of bamboo charcoal (BC) and the influence of BC on nitrogen retention at different soil depths using multi-layered soil columns. Results showed that BC could adsorb ammonium ion predominantly by cation exchange. Ammonium nitrogen (NH₄ ⁺-N) concentrations in the leachate of the soil columns showed significant differences at different depths after ammonium chloride application to the columns depending on whether BC had been added. Addition of 0.5% BC to the surface soil layer retarded the downward transport of NH₄ ⁺-N in the 70-day experiment, as indicated by measurements made during the first 7 days at 10 cm, and later, in the experimental period at 20 cm. In addition, application of BC reduced overall cumulative losses of NH₄ ⁺-N via leaching at 20 cm by 15.2%. Data appeared to suggest that BC could be used as a potential nutrient-retaining additive in order to increase the utilization efficiency of chemical fertilizers. Nonetheless, the effect of BC addition on controlling soil nitrogen losses through leaching needs to be further assessed before large-scale applications to agricultural fields are implemented.     

Variations in concentrations of N and P forms in leachates from dried soils rewetted at different rates

The rate at which dried soils are rewetted can affect the quantities and forms of nutrients in leachates. Both dried and moist replicated (n?=?3) samples of two contrasting grassland soil types (clayey vs brown earth) were irrigated during laboratory experiments with identical total amounts of water, but at different rates, ranging from 0 h, increasing by 30-min increments up to 4 h, and additionally a 24-h rewetting rate. Total P concentrations in leachates from dried samples of both soils generally decreased as rewetting rate increased, ranging from 2,923?±?589 μg P L^?1 (0.5 h rewetting rate) to 731?±?46.0 μg P L^?1 (24 h, clayey soil) and 1,588?±?45.1 μg P L^?1 (0.5 h) to 439?±?25.5 μg P L^?1 (24 h brown earth). Similar patterns in concentrations occurred for molybdate reactive P (MRP), although concentrations were generally an order of magnitude lower, indicating that the majority of the leached P was probably organic. The moist brown earth leached relatively high concentrations of MRP (maximum 232?±?10.6 μg P L^?1, 0.5 h), unlike the moist clayey soil (maximum 20.4?±?10.0 μg P L^?1, 0 h). The total oxidised N concentrations in leachates were less affected by rewetting rate, although longer rewetting rates resulted in decreased concentrations in leachates from the dried samples of both soils. The difference in responses to rewetting rates of the two soils is probably due to differences in the fate of the microbial biomass and adsorption properties in the soils. Results show that soil moisture could be an important factor in regulating nutrient losses and availability, especially under changing patterns of rainfall predicted by future climate change scenarios.     

Environmental impact of two organic amendments on sorption and mobility of propachlor in soils

Purpose

The purposes of this study were to understand the sorption?Cdesorption characteristics of propachlor in three types of soils with added solid organic matters and the effect of solid organic matters on propachlor mobilization in soil microstructures.

Materials and methods

Three soil types, Eutric gleysols (EG), Hap udic cambisols (HUC), and Haplic alisol (HA), along with the lakebed sludge (SL) and pig manure compost (PMC), were used in the study. The sorption and desorption experiments were carried out using the standard batch equilibration method. Soil column leaching was performed with soil samples packed into PVC columns. Soil thin-layer chromatography was performed using soils and water mixture spread on a 0.5?C0.7-mm thick layer over 20?×?10-cm glass plates.

Results and discussion

Propachlor was shown to be more mobile in EG and HUC than in HA. Application of PMC and SL to soils affected the propachlor mobilization in the soils. Using batch experiment, soil column, and soil thin-layer chromatography, we showed that addition of SL and PMC increased the sorption and decreased desorption of propachlor in the soils. Addition of PMC and SL reduced the total concentration of propachlor in the soil leachate and migration of propachlor in the soil profiles. Physicochemical properties of the three soils were analyzed and showed that the content of organic carbon (in percentage) was higher in Haplic alisol than in Eutric gleysols and Hap udic cambisols.

Conclusion

The soil organic matter played critical roles in modifying the absorption and mobility of organic chemicals (e.g., herbicide and contaminants) in soil ecosystem.     

Heavy Metals in Water Percolating Through Soil Fertilized with Biodegradable Waste Materials

The influence of manure and composts on the leaching of heavy metals from soil was evaluated in a model lysimeter experiment under controlled conditions. Soil samples were collected from experimental fields, from 0- to 90-cm layers retaining the layout of the soil profile layers, after the second crop rotation cycle with the following plant species: potatoes, spring barley, winter rapeseed, and winter wheat. During the field experiment, 20 t DM/ha of manure, municipal sewage sludge composted with straw (SSCS), composted sewage sludge (SSC), dried granular sewage sludge (DGSS), “Dano” compost made from non-segregated municipal waste (CMMW), and compost made from municipal green waste (CUGW) was applied, i.e., 10 t DM/ha per crop rotation cycle. The concentrations (μg/dm³) of heavy metals in the leachate were as follows: Cd (3.6–11.5)?<?Mn (4.8–15.4)?<?Cu (13.4–35.5)?<?Zn (27.5–48.0)?<?Cr (36.7–96.5)?<?Ni (24.4–165.8)?<?Pb (113.8–187.7). Soil fertilization with organic waste materials did not contaminate the percolating water with manganese or zinc, whereas the concentrations of the other metals increased to the levels characteristic of unsatisfactory water quality and poor water quality classes. The copper and nickel content of percolating water depended on the concentration of those metals introduced into the soil with organic waste materials. The concentrations of Cd in the leachate increased, whereas the concentrations of Cu and Ni decreased with increasing organic C content of organic fertilizers. The widening of the C/N ratio contributed to Mn leaching. The concentrations of Pb, Cr, and Mn in the percolating water were positively correlated with the organic C content of soil.