Effect of freeze–thaw cycles on carbon stocks of saline–alkali paddy soil

This study aims to provide basic data to support accurate estimation of carbon stocks and reveal the physicochemical factors that influence the carbon cycle in saline–alkali soils. Soil samples were collected during initial freezing, complete freezing, initial thawing and complete thawing stages. Levels of soil organic carbon (SOC), soil inorganic carbon (SIC), moisture, salinity, pH and available nitrogen were determined, and variations were observed during the freezing and thawing periods. Correlation analysis and regression analysis of carbon contents and physicochemical properties were performed. The results showed that freeze–thaw cycles have significant effects on carbon contents. The SOC content initially decreased in the freezing stage and then increased in the thawing stage. However, the SIC content initially increased in the freezing stage, decreased in the initial thawing stage and finally increased in the complete thawing stage. The migration and transformation of SOC and SIC were observed both temporally and spatially. SOC was positively correlated with available nitrogen, moisture and salinity and negatively correlated with pH; while SIC was negatively correlated with available nitrogen, moisture and salinity and positively correlated with pH. Among the factors evaluated, available nitrogen and salinity exerted the greatest effects on SOC and SIC contents, respectively.     

Application of Electrochemical Degradation of Wastewater Composed of Mixtures of Phenol–Formaldehyde

The industrial wastewater from resin production plants contains as major components phenol and formaldehyde, which are traditionally treated by biological methods. As a possible alternative method, electrochemical treatment was tested using solutions containing a mixture of phenol and formaldehyde simulating an industrial effluent. The anode used was a dimensionally stable anode (DSA?) of nominal composition Ti/Ru_0.3Ti_0.7O₂, and the solution composition during the degradation process was analyzed by liquid chromatography and the removal of total organic carbon. From cyclic voltammetry, it is observed that for formaldehyde, a small offset of the beginning of the oxygen evolution reaction occurs, but for phenol, the reaction is inhibited and the current density decreases. From the electrochemical degradations, it was determined that 40?mA?cm^?2 is the most efficient current density and the comparison of different supporting electrolytes (Na₂SO₄, NaNO₃, and NaCl) indicated a higher removal of total organic carbon in NaCl medium.     

Integrated Analysis of Capture–Recapture–Resighting Data and Counts of Unmarked Birds at Stop-Over Sites

The models presented in this paper are motivated by a stop-over study of semipalmated sandpipers, Calidris pusilla. Two sets of data were collected at the stop-over site: a capture–recapture–resighting data set and a vector of counts of unmarked birds. The two data sets are analyzed simultaneously by combining a new model for the capture–recapture–resighting data set with a binomial likelihood for the counts. The aim of the analysis is to estimate the total number of birds that used the site and the average duration of stop-over. The combined analysis is shown to be highly efficient, even when just 1 % of birds are recaptured, and is recommended for similar investigations. This article has supplementary material online.     

Comparison of thermal and chemical stability of Cu–humic complexes

Purpose

The purpose of this study was to investigate relationships between chemical and thermal stabilities of Cu–humic complexes. The study of the chemical stability was based on pedological methods used for the determination of the bond strength of metal ions in soils by chemical leaching agents. The samples with various contents of the Cu(II) ions and their bond strength were put to the thermal analysis in order to correlate their thermo-oxidative behavior with their stability determined by leaching.

Materials and methods

The humic acid was extracted from the South-Moravian lignite by standard alkaline extraction. The humic sample was used in two different forms: as the solid powder and as the hydrogel prepared by the acidic precipitation of humate. Six various concentrations of copper(II) solutions were used for the complexation of the humic powder and the hydrogel, in order to study the influence of their initial concentration on both the determined stabilities of the prepared complexes. Their chemical stability was assessed in terms of the Cu(II) ions release from the humic acid structure into two different extraction agents (MgCl₂ and HCl solutions). Their thermo-oxidative behavior was investigated employing the thermogravimetry.

Results and discussion

The complexation capacity of the humic hydrogel was higher in comparison with the humic powder. The amounts extractable from the Cu–humic complexes by the used leaching agents are higher for the humic powder, which shows on the lower chemical stability. The thermal degradation of the prepared complexes proceeds in several steps and this character remains also after the removal of the mobile and the ion-exchangeable fractions by the MgCl₂. The elimination of these fractions as well as the extraction of the strongly bound Cu(II) ions shift the thermal degradation to higher temperatures. The incombustible residue increases with the Cu(II) content in the complexes except for the samples extracted by the HCl.

Conclusions

The form of humic sample used for the preparation of the Cu–humic complexes influences both the chemical stability and the thermal one. The main reason is probably a better accessibility of the functional groups in the humic gel, which enables forming stronger binding copper(II) ions. The results showed that the thermal and chemical stabilities are closely related, which corresponds with the shift of the thermal degradation to higher temperatures after removing the less stable fractions from the humic complexes.     

Potential of Carbon Dioxide Biosequestration of Saline–Sodic Soils during Amelioration under Rice–Wheat Land Use

Potential for carbon dioxide (CO₂) biosequestration was determined during the reclamation of highly saline–sodic soils (Aridisols) after rice (2003) and wheat (2003–2004) crops at two sites in District Faisalabad, Pakistan. Two treatments were assessed: T₁, tube-well brackish water only; and T₂, soil-applied gypsum at 25% soil gypsum requirement?+?tube-well brackish water. The irrigation water used at both sites had different levels of salinity (EC 3.9–4.5 dS m^?1), sodicity (SAR 21.7–28.8), and residual sodium carbonate (14.9 mmol_c L^?1). Composite soil samples were collected from soil depths of 0–15 and 15–30 cm at presowing and postharvest stages and analyzed for pH, EC_e, and sodium adsorption ratio (SAR). After rice harvest, there was no significant effect of gypsum application on EC_e, pH, and SAR at both sites, except pH at 0–15 cm depth decreased significantly with gypsum at site 1. After wheat harvest, EC_e, pH, and SAR decreased significantly with gypsum at site 1, whereas the effect of gypsum on these parameters was not significant at site 2. Compared to initial soil, EC_e and SAR in soil decreased considerably after rice or wheat cultivation, particularly at site 1, whereas pH increased slightly due to cultivation of these crops. For rice, the total CO₂ sequestration was significantly increased with gypsum application at both sites and ranged from 1499 to 2801 kg ha^?1. The total sequestration of CO₂ was also significantly increased with gypsum application in wheat at both sites and ranged from 2230 to 3646 kg ha^?1. The amounts of CO₂ sequestered by crops due to gypsum application were related to seed and straw yield responses of rice and wheat to gypsum, which were greater at site 1 than site 2. Also, the yield response to applied gypsum was greater for rice than wheat at site 1, whereas the opposite was true at site 2. Overall, the combined application of gypsum with brackish water reduced soil EC_e and SAR compared to brackish water alone, particularly at site 1. Our findings also suggest that the reclamation strategies should be site specific, depending on soil type and quality of brackish water used for irrigation of crops. In conclusion, the use of gypsum is recommended on brackish water–irrigated salt-prone soils to improve their quality, and for enhancing C biosequestration and crop production for efficient resource management.     

Treatment of Olive Oil Mill Wastewater by Silica–Alginate–Fungi Biocomposites

Olive oil mill wastewater (OMW) generates a wide variety of pollutants depending on the production process and other factors such as olive varieties and cultivation system. Efforts to mitigate the impact of these effluents in the environment have been made by developing more efficient treatment systems in terms of removal of chemical oxygen demand (COD), color, organic compounds, and toxicity. This study is the first that reports the potential of a treatment of OMW by biocomposites of silica?Calginate?Cfungi (Pleurotus sajor caju and Trametes versicolor). The treatment by biocomposites can be considered as a three-step process responsible for the removal of the compounds: (1) adsorption of reactants on the monolithic structure and diffusion to the biological active sites, (2) biodegradation by the fungi, and (3) diffusion of the products resulting from the biodegradation. Both treatments tested showed potential capacity to remove organic compounds, color, COD, and toxicity. The T. versicolor biocomposites were the most effective and responsible for the reduction in color (from 38.4 to 44.9?%), COD (from 42.8 to 63.8?%), and total phenolic content (from 85.3 to 88.7?%) after 29?days of treatment. The toxicity reduction on Portuguese OMW was minimal, but the use of composites on the Moroccan OMW caused a 9.5- to 19-fold reduction in toxicity. Furthermore, the biocomposites showed potential for re-utilization for more 29?days of treatment.     

Calibration of Hargreaves–Samani and Priestley–Taylor equations in estimating reference evapotranspiration in the Northwest of Iran

Accurate estimation of reference evapotranspiration (ET_o) is essential for water resources management and irrigation systems scheduling, especially in arid and semiarid regions such as Iran. In the present research, constant coefficients of Hargreaves–Samani (C_H–S) and Priestley–Taylor (C_P–T) equations were locally calibrated to estimate the ET_o based on the FAO–Penmen–Monteith (PM) method as standard method. For this purpose, meteorological data of eight synoptic stations located in the northwest of Iran were used during the period of 1997–2008. The outcomes showed that the values of C_H–S and C_P–T were 0.0026 (instead of 0.0023) and 1.68 (instead of 1.26), respectively. Also, at stations with high wind speed, the values of calibrated coefficients of C_H–S and C_P–T were maximum. Then, the estimated ET_o values using adjusted C_H–S and C_P–T coefficients were compared to the obtained actual ET_o values by PM method using root mean square error and mean bias error indices. The results indicated that the new calibrated H–S and P–T equations have good agreement with the PM method for estimation of the ET_o. Moreover, the equation of Ravazzani et al. was calibrated in the studied region. It was concluded that in general, the mentioned equation was shown better performance than original H–S equation.     

Effect of microwave–chemical pre-treatment on compression characteristics of biomass grinds

The effect of microwave and microwave–chemical pre-treatments on densification characteristics and physical quality of pellets made from wheat and barley straw grinds were investigated. The ground wheat and barley straw samples were immersed in water, sodium hydroxide or calcium hydroxide solution at different concentrations (1 and 2% w/v) and then exposed to microwave radiation at three power levels (295, 603 and 713 W). Chemical composition and bulk and particle densities of samples were determined after pre-treatments. Pre-treated grinds were compressed in a plunger–die assembly with a force of 4000 N and compression and relaxation test data were recorded. The specific energy required for compression and ejection of pellets produced from untreated and pre-treated wheat and barley straw grinds was calculated. The tensile strength of the pellets was also evaluated to investigate the hardness of the pellets. Chemical composition analysis showed that microwave and chemical pre-treatment was significantly able to disintegrate the lignocellulosic structure of wheat and barley straw grinds. Data analysis also indicated that the pellets made from microwave–chemical pre-treated biomass grinds had a significantly higher density and tensile strength than the untreated or samples pre-treated by microwave and distilled water.     

Landau–Deryagin law and hydration energy of soils of different genesis

Linear regression equations between the logarithm of the total soil moisture potential and soil moisture content in the hygroscopic moisture range (Landau–Deryagin law) were derived for typical soils from different natural zones of European Russia. From these equations, a compact algorithm was developed for calculating the hydration energy of soils, which increases from 1280 to 10600 J/kg in the following soil series: heavy loamy soddy podzolic soil–heavy loamy gray forest soil–medium loamy light chestnut soil–heavy loamy brown semidesert soil–light clayey solonchak–light clayey chernozem–medium clayey krasnozem. Relationships were revealed between the hydration energy of soils, the specific surface of soils, the content of physical clay in soils, and the concentration of hydrated exchangeably adsorbed ions.     

Interaction of Magnesium–Iron–Carbonic-Layered Double Hydroxides with As(III)

Static granular bed reactor (SGBR) and upflow anaerobic sludge blanket (UASB) reactor were demonstrated at mesophilic condition for the treatment of pulp and paper mill wastewater. The hydraulic retention times (HRTs) were varied from 4 to 24 h following 29-day start-up period. The overall chemical oxygen demand (COD) removal efficiency of the SGBR was higher than the UASB during this study. At 4 h HRT, the COD removal was greater than 70 % for the SGBR and 60 % for the UASB. Biomass yield and volatile fatty acids concentration of SGBR were slightly less than UASB at organic loading rates ranging from 1.2 to 5.1 kg/m³/day. The results indicated that the SGBR system can be considered a viable alternative system for anaerobic treatment for pulp and paper wastewater.     

15N2–DNA–stable isotope probing of diazotrophic methanotrophs in soil

Nucleic acid stable isotope probing (SIP) is a powerful tool that can identify and characterize the microorganisms that mediate specific soil processes and explore the flow of C and N through functional groups in the soil food web. While ¹³C–SIP has been used successfully in a range of applications, methodological constraints have limited the applicability of ¹⁵N-labelled compounds in nucleic acid SIP. However, ¹⁵N–DNA–SIP can now be achieved and this method when used with ¹⁵N₂ provides a powerful new tool for characterizing free-living diazotrophs in natural ecosystems. A diverse array of non-cultivated diazotrophs have been observed in soil and yet the characteristics of these organisms and their environmental significance remain almost completely unknown. ¹⁵N₂–DNA–SIP can identify those diazotrophs that are active in situ while providing access to gene sequences and genome fragments that can yield insights on their evolutionary history and functional capacities. Further insights on the ecology of free-living diazotrophs in soil can be provided by performing ¹⁵N₂–DNA–SIP on microcosms in which the response of the diazotrophic community is determined in relation to experimental manipulation. We describe the use of ¹⁵N₂–DNA–SIP to explore linkages between different C sources and N-fixation by specific diazotroph populations in soil. Methane addition to soil was observed to stimulate N-fixation and the organisms that were found to be responsible for this activity were Type II methanotrophs most closely related to the genus Methylocystis. This report provides insights on the use of nucleic acid SIP to identify and characterize microorganisms that mediate specific soil processes and represents the first time that a specific group of methanotrophs has been shown to mediate N-fixation while in the soil environment.     

Long–term effect of crop rotation and nutrient management on soil–plant nutrient cycling and nutrient budgeting in Indo–Gangetic plains of India

In the present investigation, the long-term effect of pulse crop inclusion in the maize-wheat rotation was assessed for the nutrient availability and soil-plant nutrient cycling under different nutrient management practices. Including pulses in the maize-wheat rotation improved soil organic carbon (SOC) and plant available macronutrients being higher in maize-wheat-mungbean rotation. Inclusion of mungbean to maize-wheat rotation enhanced the nitrogen (33.9%), phosphorus (46.4%), potassium (36.3%), and sulphur (55.5%) uptake in maize crop; likewise, alternate-year chickpea inclusion increased the uptake of these nutrients by 18.2, 19.1, 21.7, 32.1%, respectively. Inorganic fertilization maintained the positive annual balance of nitrogen, phosphorus, and zinc. By contrast, the nutrient balance under organic nutrient management was mostly negative. The magnitude of negative balance of potassium and sulphur was higher in inorganic than that of organic nutrient management. The low nutrient supply (particularly nitrogen) in organic fertilization largely inhibited the yield of cereal crops but not that of pulses. In view of this, the inclusion of pulses in the cereal-cereal systems could cause substantial improvement in soil fertility and sustainability in Indo-Gangetic plains. We infer that supply of nutrients like nitrogen and phosphorus in organic, and potassium and sulphur in recommended inorganic fertilization merit special attention.     

Effect of SDBS–Tween 80 mixed surfactants on the distribution of polycyclic aromatic hydrocarbons in soil–water system

Purpose

Enhancing desorption of hydrophobic organic contaminants from soils is a promising approach for the effective remediation of soils contaminated with organic compounds. The desorption efficiency of chemical reagent, such as surfactant, should be evaluated. In this study, the effect of mixed anionic–nonionic surfactants sodium dodecylbenzene sulfonate (SDBS)–Tween 80 on the distribution of polycyclic aromatic hydrocarbons in soil–water system was evaluated.

Materials and methods

Batch desorption experiments were employed to evaluate the distribution of polycyclic aromatic hydrocarbons (PAHs) and surfactants in soil–water system. PAHs and SDBS were determined by high-performance liquid chromatography, Tween 80 by spectrophotometry, and total organic carbon with a carbon analyzer.

Results and discussion

Sorption of PAHs to soil was increased at low surfactant concentration due to the effective partition phase on soil formed by sorbed surfactants. The mixture of anionic and nonionic surfactants decreased the sorption of surfactants to soil, increasing the effective surfactant concentration in solution and thus decreasing the sorption of PAHs on soil. Anionic–nonionic mixed surfactant showed better performance on desorption of PAHs from soil than single surfactant. The greatest desorption efficiency was achieved with low proportions of SDBS (SDBS/Tween80?=?1:9).

Conclusions

SDBS–Tween 80 mixed surfactant showed the highest desorption rate with low proportion of SDBS, which indicated that the addition of relative low amount of anionic surfactant could significantly promote the desorption efficiency of PAHs by nonionic surfactants. Results obtained from this study did provide useful information in surfactant-enhanced remediation of soil and subsurface contaminated by hydrophobic organic compounds.     

Quantifying effects of primary parameters on adsorption–desorption of atrazine in soils

Purpose

Adsorption and desorption are important processes that influence the transport, transformation, and bioavailability of atrazine in soils. Equilibrium batch experiments were carried out to investigate the adsorption–desorption characteristics of atrazine. The objectives of this study were to (1) determine and quantify the main soil parameters governing atrazine adsorption and desorption phenomena; (2) find the correlativity between the identified soil parameters; and (3) investigate the universal desorption hysteresis traits.

Materials and methods

Fifteen soils with contrasting physico-chemical characteristics were collected from 11 provinces in eastern China. The equilibrium time was 24 h both for adsorption and desorption experiments. Atrazine was detected by Waters 2695/UV HPLC.

Results and discussion

Adsorption isotherms of atrazine could be well described by the Freundlich equation (r?≥?0.994, p?<?0.01). The total organic carbon (TOC) was the first independent variable that described 53.0 % of the total variability of K _f, followed by the pH (9.9 %), and the clay (4.0 %) and silt (1.2 %) contents, separately; while the primary soil properties that affect desorption parameters included the TOC, pH, free Fe₂O₃ (Fe_d) and the sand content, with the biggest contribution achieved by the TOC (ranged from 48.5–78.1 %). The results showed that when the content ratio of clay to TOC (RCO) was less than 40, the atrazine adsorption was largely influenced by the organic matrix, while when the RCO was greater than 40, they were vital affected by the clay content.

Conclusions

Adsorption–desorption isotherms of atrazine in soils were nonlinear. The content of TOC, clay, and iron oxides, as well as the pH value were the key soil parameters affecting the adsorption–desorption of atrazine in soil, among which the RCO especially exhibited relevance. Additionally, the desorption hysteresis existed for atrazine retention in all 15 tested soils, and the hysteretic effect enhanced with the increasing time for desorption. This would be ascribed to the heterogeneity physical–chemical properties of these soils.     

Tea Plantation–Induced Activation of Soil Heavy Metals

Abstract

The accumulation of heavy metals in tea leaves is of concern because of its impact on tea quality. This study characterized long‐term changes of soil properties and heavy‐metal fractions in tea gardens and their effect on the uptake of metals from soils by the plants. Soil and tea leaf samples were collected from five plantations with a history of 2–70 years in Jinghua, Zhejiang Province, southeast China. The six chemical fractions (water‐soluble, exchangeable, carbonate‐bound, organic‐matterbound, oxide‐bound, and residual forms) of cadmium (Cd), chromium (Cr), copper (Cu), iron (Fe), nickel (Ni), manganese (Mn), lead (Pb), and zinc (Zn) in the soils were characterized. Dissolved organic‐matter accumulation in the soils and effects of low‐molecular‐weight organic acids on solubility of soil heavy metals were also tested. Long‐term tea plantation use resulted in accumulation of dissolved organic matter, decrease of soil pH, and elevation of water‐soluble and exchangeable metal fractions, thereby increasing metal contents in leaves. The influence was more significant when soil pH was less than 4.4. The results indicated that both acidification and accumulation of dissolved organic matter induced by tea plantations were also important causes of increased accumulation of the metals in the tea leaves. This was particularly true for the soils polluted with low concentration of heavy metals, because availability of the metals in these soils was mainly controlled by pH and dissolved organic matter.     

Soil–Phosphorus Mobilization Potential of Phytate Mineralizing Fungi

Four most efficient phytase and phosphatase producing fungi belonging to genera Aspergillus, Trichoderma, and Penicillium were isolated from the rhizosphere soil of leguminous, cereal, and vegetable crops. Efficacy order of fungi in terms of phytate hydrolysis under laboratory conditions was Aspergillus > Penicillium > Trichoderma. The test fungi released more of extracellular (E) phytase than intracellular (I) phytase (E: I- 3.44 - 6.03:1) and produced acid phosphatase activity ranging from 367- 830 μmol pNP ml^?1 h^?1. Aspergillus niger possessed the twin ability of phosphate mineralization and solubilization. The incubation studies in compost-amended soil exhibited the higher competence of Penicillium chrysogenum to improve the soil available P and increase the level of extractable organic P under alkaline soil to benefit P nutrition. Developing microbial inoculant using P. chrysogenum strain and its subsequent application to soil may help the marginal farmer to replenish soil P more economically compared to chemical fertilizer.     

Meeting the challenge of scaling up processes in the plant–soil–microbe system

The scaling up of processes in the plant–soil–microbe system represents one of the greatest challenges facing environmental scientists and yet is essential for sustainable land management worldwide. The latter encompasses, for example, the mitigation of and adaptation to anthropogenic climate change, the bioremediation of industrially contaminated sites, catchment management of human pathogens such as Escherichia coli O157 and integrated crop management on the farm. Scaling up is also essential for the regional and global biogeochemical modelling that will inform policy-makers of the critical environmental factors driving climate change. Despite increasing understanding of the links between gene expression and process on a microscale, there is still much progress to be made when relating this to processes at the macroscale. In this paper, we explore the challenges this poses and examine key case studies of successful up-scaling.

Evaluation of the Migration Capacity of Zn in the Soil–Plant System

The mobility and migration capacity of Zn in the soil-plant system were studied in a series of pot experiments with barley as a test plant. The parameters of Zn accumulation depending on the metal concentrations in soils and soil solutions were estimated by soil and water culture methods. Experiments with barley in water culture were performed on a nutrient (soil) solution extracted from soddy-podzolic soil (Albic Retisol (Loamic, Ochric)) to which Zn²⁺ was added to reach working concentrations increasing from 0.07 to 430 μM. Different responses of barley plants to changes in the concentration of Zn in the studied soil were identified. Ranges of the corresponding concentrations in the soil and aboveground barley biomass were determined. Parameters of Zn accumulation by test plants were determined depending on the metal content in soddypodzolic soil and the soil solution. A new method was proposed for evaluating the buffer capacity of soils with respect to a heavy metal (Zn) using test plants (BCS(P)_Zn). The method was used to evaluate the buffering capacity of loamy sandy soddy-podzolic soil. The considered methodological approach offers opportunities for using data obtained during the agroecological monitoring of agricultural lands with heavy metals (HMs), including the contents of exchangeable HMs and macroelements (C and Mg) in soils and concentrations of HMs and (Ca + Mg) in plants, in the calculation of the buffering capacity of the surveyed soils for HMs.