Purpose

The increasing reuse of wastewater for irrigation introduces surfactants and antibiotics into the environment. How these two kinds of compounds interact with regard to their sorption processes in soil is not clear.

Materials and methods

We performed batch experiments to investigate the sorption of linear alkylbenzene sulfonates (LAS) and its effect on sorption of sulfamethoxazole and ciprofloxacin in irrigated and non-irrigated soils with different organic matter (OM) contents.

Results and discussion

LAS sorption was non-linear in the presence of the antibiotics, and as general trend, it increased with rising OM content of soils. Free LAS was also removed from solution by complexation with Ca²⁺. Dissolved organic compounds released from soils with OM contents ≥18.4 g kg^?1 further reduced LAS sorption. Sorption of sulfamethoxazole was reduced by LAS sorption only in one soil with a small OM content of 9.5 g kg^?1.

Conclusions

The strong sorption of ciprofloxacin is not affected by LAS. Sulfamethoxazole sorption only competes with LAS sorption in organic matter-poor soils. Accumulation of organic matter in soils, for example due to long-term wastewater irrigation, provides extra sorption capacity for LAS and sulfamethoxazole so that competition for sorption sites is reduced.

Purpose

Sulfamethazine (SMT) is increasingly detected in environmental matrices due to its versatile use as antibiotics. We aimed to investigate the benefits and roles of steam activation of biochars with respect to SMT sorption kinetics and equilibrium sorption.

Materials and methods

Biochars were produced from burcucumber plant and tea waste using a pyrolyzer at a temperature of 700 °C for 2 h. The biochar samples were treated with 5 mL min^?1 of steam for an additional 45 min for post-synthesis steam activation. The SMT sorption on the unmodified and steam activated biochars were compared.

Results and discussion

The time taken to reach equilibrium was significantly less for steam activated biochars (～4 h) than non-activated biochars (>24 h). Up to 98 % of SMT could be removed from aqueous solutions by steam activated biochars. The sorption kinetic behaviors were well described by the pseudo-second model and SMT sorption rates of steam activated biochars (k ₂?～?1.11–1.57 mg g^?1 min^?1) were significantly higher than that of the unmodified biochars (k ₂?～?0.04–0.11 mg g^?1 min^?1) because of increased availability of accessible porous structure with averagely larger pore diameters. Moreover, the equilibrium sorption on the unmodified biochars was significantly influenced by increasing solution pH (～30–50 % reduction) because of speciation change of SMT, whereas steam activated biochars manifested much stronger sorption resilience against pH variation (～2–4 % reduction only) because the enhanced porosity offset the effect of unfavorable electrostatic repulsion.

Conclusions

The observed features of steam activated biochars would render their applications more versatile and reliable in field throughout changeable environmental conditions.

Purpose

Remediate metal contamination is a fundamental step prior to reclaim oil sands tailing ponds, and copper (Cu(II)) is the most abundant metal in the tailings water or oil sands process-affected water (OSPW). Biochars produced at four pyrolysis conditions were evaluated for sorption of Cu(II) in synthetic OSPW to explore different biochar potentials in removing Cu(II) from the contaminated water.

Materials and methods

Pine sawdust biochars pyrolyzed at 300 and 550 °C with and without steam activation were investigated by batch sorption experiments. Isotherm and kinetic studies were conducted to compare the sorption capacities of the four biochars and to examine potential mechanisms involved.

Results and discussion

For all the biochars, Langmuir and pseudo-second order models were the best-fit for isotherm and kinetic studies, respectively. According to the Langmuir parameters, the maximum adsorption capacities of the biochars produced at 550 °C were around 2.5 mg Cu(II)?g^?1, which were 30-folds higher than those produced at 300 °C. However, steam activation did not cause any significant difference in the biochars’ sorption performance. The kinetic study suggested that chemisorption involving valence forces was the limiting factor of the sorption. In addition, ion exchange and precipitation were likely the primary mechanisms for Cu(II) sorption which outweigh complexation with functional groups on the biochars’ surface.

Conclusions

Pine sawdust biochar produced at 550 °C without steam activation could be utilized as a sustainable and cost-effective material to remove Cu(II) from the OSPW.

Purpose

Technosol management is one of the greatest challenges for the future, more specifically as regards supporting and/or restoring ecosystems. The understanding of natural soil organic matter (SOM) dynamic from Technosol may give important information about soil functioning and Technosol evolution.

Materials and methods

According to this, SOM from three French old mine Technosols, (an old tin mine, a lead and zinc, and a gold one which is arsenic-rich), were studied and characterized using thermochemolysis coupled with gas chromatography and mass spectrometry (GC-MS) with tetramethyl ammonium hydroxide (TMAH) as reagent and FTIR. The characterization and quantification of some specific biomacromolecules, used as biomarkers, indicate the specific level of incorporation relative to various subgroups. Global parameters of soils (pH, total organic matter, cation exchange capacity…) were also evaluated.

Results and discussion

Results on bulk samples show that lipids are the most reactive group and therefore play the most important role in young soil pedogenesis. All of the results show that the behavior of SOM of the Technosol is similar to homolog non-anthropized soil and depends on vegetation type.

Conclusions

A slight inhibition of bacterial activity is observed which underlines a protective effect of Technosols on SOM degradation due to the low pH, the high clay content, and the presence of Al³⁺ and metal(loid)s. In fine, lipid fraction of SOM may act as a well-done fingerprint of pedogenesis processes in Technosols.

Purpose

Combined pollution by polycyclic aromatic hydrocarbons (PAHs) and heavy metals are commonly found in industrial soils. This study aims to investigate the effect of the coexistence of heavy metals on the sorption of PAHs to soils. We focused specifically on the relationship of the sorption capacity with the estimation of the binding energy between PAHs and heavy metals.

Materials and methods

The sorption of typical PAHs (naphthalene, phenanthrene, and pyrene) to soils coexisting with heavy metals (Cu(II), Pb(II), and Cr(III)) was characterized in batch sorption experiments. The binding energy between PAHs and heavy metals in aqueous solution was estimated by quantum mechanical (QM) method using density functional theory (DFT) at the M06-2x/def2svp level of theory.

Results and discussion

Sorption capacity and nonlinearity of the PAHs to the soils were enhanced by the coexisting heavy metals. The extent of increment was positively associated with the hydrophobicity of the PAHs and the electronegativity and radius of the metal cations: Cr(III)?>?Pb(II)?>?Cu(II). The cation-π interaction was revealed as an important noncovalent binding force. There was a high correlation between the binding energies of the PAHs and K _f ′ (K _f adjusted after normalizing the equilibrium concentration (C _e) by the aqueous solubility (C _s)) (R ²?>?0.906), indicating the significant role of the cation-π interactions to the improved PAH sorption to soils.

Conclusions

In the presence of heavy metals, the sorption capacities of naphthalene, phenanthrene, and pyrene to soils were enhanced by 21.1–107 %. The improved sorption capacity was largely contributed from the potent interactions between PAHs and heavy metals.

Purpose

Quarrying activities in areas with serpentinized rocks may have a negative impact on plant growth. Quarry soils generally offer hostile environments for plant growth due to their low-nutrient availability, low organic matter, and high-trace metal content.

Materials and methods

In order to determine the factors that can limit plant revegetation, this study was carried out in two serpentine quarries in Galicia (NW Spain): one abandoned in 1999 and the other still active.

Results and discussion

The results show that in soils developed in the abandoned quarry, the limitations for revegetation were: moderate alkaline pH (7.87–8.05), strong Ca/Mg (<1) imbalance, low N (<0.42 mg kg^?1) and P (<2 mg kg^?1) content, and high total heavy-metal content (Co 76–147 mg kg^?1; Cr 1370–2600 mg kg^?1; and Ni 1340–2040 mg kg^?1). The limitations were much less intense in the soils developed in the substratum in the active quarry, which were incipient soils poorly developed and permanently affected by the quarrying activity.

Conclusions

Restoration work should be geared toward establishing a stable diverse vegetation cover, including serpentinophile species, which would provide the necessary modifications to correct nutritive imbalances and improve soil quality.

Purpose

Sulfonamides are widely used for the prevention and treatment of bacterial infections, hard-degraded contaminants distributed in the environment if they are discharged into the soil and water. Biochar could probably influence the geochemical behavior of ionized antibiotics in the soils.

Materials and methods

To determine the sorption/desorption of three representative sulfonamides (SAs) in soils amended with biochar, we investigated the effects of water pH, Cu²⁺, and dissolved humic acid on the sorption of sulfamethoxazole (SMX), sulfamethazine (SMZ), and sulfadiazine (SD) onto two different soil samples (S1 pH?=?5.13 and S2 pH?=?7.33) amended with wheat straw-derived biochar (size 0.5～0.6 mm).

Results and discussion

Batch experiments showed that the sorption/desorption isotherms of SAs on soil with/without biochar followed the Freundlich model. The biochar had a strong adsorption potential for SMX, SMZ, and SD both in S1 and S2 at low water pH. Except for SMX, the presence of Cu²⁺ inhibited the sorption of SMZ and SD through competing hydrophobic adsorption region in soils. HA suppressed the sorption of three sulfonamides in soil S2 by electrostatic repulsion under alkaline condition. The soil leaching column experiments showed the SA transport in soils, and S1 and S2 amended with biochar (0.5 and 1.0 wt%) brought about 12–20 % increase in SMX, SMZ, and SD retention compared to the untreated soil.

Conclusions

The results indicated that the presence of biochar effectively mitigated the mobility of ionized antibiotics such as SMX, SMZ, and SD in soils, which helps us reconsider the potential risk of antibiotics in the environment.

Purpose

Soil macropores play a principal role in water infiltration but they are highly variable. The objectives of this study were (1) to investigate the temporal change in macropores of an Ultisol as affected by land use and slope position and (2) to analyze contribution of macropores to water infiltration.

Materials and methods

Water infiltration was measured at upper and lower slopes in citrus orchard and watermelon field once every 2 months for 1 year using tension infiltrometers at a successive pressure head from ?12, ?6, ?3, to 0 hPa.

Results and discussion

Hydraulic conductivity (K) was significantly affected by land use and slope position except at 0 hPa pressure head, showing a significant temporal variation. Effective macroporosity, derived from the increment of hydraulic conductivity between ?3 and 0 hPa, showed a significant temporal variation. Such temporal variation was land use (P?<?0.05) and slope position (P?<?0.001) dependent. Despite of low proportion in total soil volume (averaged 3.5 cm³ m^?3), the macropores contributed 47 % of water flux on average. The macroporosity was more stable and higher in the citrus orchard (2.43 cm³ m^?3, coefficient of variance (CV)?=?75 %) than in the watermelon field (1.72 cm³ m^?3, CV?=?117 %) and contributed more to infiltration in the citrus orchard (60 %, CV?=?16 %) than in the watermelon field (33 %, CV?=?43 %) as well, because tillage was operated only in the watermelon field.

Conclusions

No-tillage increased water conducting macropores but did not increase hydraulic conductivity irrespective of slope position.

Purpose

Sorption of heavy metals on soil components plays an important role in reducing their mobility and bioavailability. Organic matter is an important sorbent of heavy metals in soil. Crop residues which are important sources of soil organic matter will undergo decomposition after addition to the soil. However, few studies reported the effect of organic matter decomposition on heavy metal sorption. This study aimed to investigate the effect of straw decomposition on the sorption of Cu.

Materials and methods

Rice straw was decomposed in aerobic conditions for 1, 3, 6, and 12 months, respectively. Solid organic matter in decomposed rice straw was collected and marked OM-1, OM-3, OM-6, and OM-12, respectively. Sorption isotherms and kinetics of Cu on solid organic matter were studied by batch experiments. The sorption of Cu was calculated by the difference between the amount of Cu added initially and that remained in the supernatant. Sorption thermodynamics of Cu were studied by isothermal titration calorimetry technique. Potential mechanisms of Cu sorption were analyzed by combining the information from sorption thermodynamics, desorption experiments, and Fourier transform infrared spectroscopy observations. All sorption experiments were carried out at pH 5.0.

Results and discussion

The maximum sorption of Cu was 165.8, 170.5, 186.6, and 226.9 mmol kg^?1, and the rate constant of Cu sorption was 0.80, 0.58, 0.50, and 0.32 kg mmol^?1 h^?1 on OM-1, OM-3, OM-6, and OM-12, respectively, indicating that the maximum sorption of Cu increased while sorption rate of Cu decreased with increasing the duration of straw decomposition from 1 to 12 months. The negative values of Gibbs free energy change and positive values of enthalpy change and entropy change revealed that Cu sorption was spontaneous, endothermic in nature, and the randomness was increased during sorption. Carboxyl and hydroxyl in solid organic matter were involved in Cu sorption. The percentage of Cu desorbed by NH₄Ac from OM-1, OM-3, OM-6, and OM-12 was 45.0, 43.5, 42.8, and 37.8 %, respectively.

Conclusions

In the current study, the decomposition of straw promoted the sorption capacity but reduced the sorption rate of Cu on solid organic matter. Copper sorption was an endothermic and spontaneous process. The formation of inner-sphere complexes was the main mechanism of Cu sorption, and its role in Cu sorption tended to increase with increasing the duration of straw decomposition. The information will facilitate the understanding of the contamination and remediation of heavy metal in cropland.

Purpose

A study was carried out to evaluate the concentration of heavy metals (Pb, Cu, Cr, Cd, and Hg) and total petroleum hydrocarbons (TPH) in road-deposited sediments (RDS) from Tijuana, Mexico, and identify their possible sources.

Materials and methods

Thirty RDS samples were randomly collected during the dry season using a brush and dustpan and classified according to construction material, traffic intensity, and land use. Soil samples were collected from a nonurban area and their concentrations were used as background values. For TPH, the samples were quantified gravimetrically after Soxhlet extraction, whereas heavy metals were extracted by acid digestion and their concentrations were measured by atomic absorption spectrometry.

Results and discussion

The mean TPH concentrations for RDS were 4208 mg kg^?1 and ranged from 1186 to 9982 mg kg^?1. For heavy metals, mean concentrations were 31.8, 50.2, 17.1, 0.1, and 0.1 mg kg^?1 for Pb, Cu, Cr, Cd, and Hg, respectively. The Igeo results showed that RDS from Tijuana are moderately to strongly polluted with Pb and Cu and moderately polluted with Cr. Principal component analysis (PCA) showed that Pb, Cu, and Cr could have their origin in tire wear, brake pads, bearings, and bushings.

Conclusions

The findings of this study revealed that RDS from Tijuana are polluted with TPH and heavy metals and that their principal sources are anthropogenic activities.

Purpose

In situ immobilization of heavy metal-contaminated soils with the repeated incorporation of amendments can effectively reduce the bioavailability of soil heavy metals. However, the long-term application of amendments would lead to the destruction of soil structure and accumulation of soil toxic elements, ultimately affecting food security and quality. Thus, the sustainability of the amendments in a heavy metal-contaminated soil was evaluated from 2010 to 2012.

Materials and methods

Batch field experiments were conducted in the soils, which were amended with apatite (22.3 t ha^?1), lime (4.45 t ha^?1), and charcoal (66.8 t ha^?1), respectively. The amendments were applied only one time in 2009, and ryegrass was sown each year. Ryegrass and setaria glauca (a kind of weed) were harvested each year. Concentrations of copper (Cu) and cadmium (Cd) were determined by batch experiments. Five fractions of Cu and Cd were evaluated by a sequential extraction procedure.

Results and discussion

Ryegrass grew well in the amended soils in the first year, but it failed to grow in all the soils in the third year. However, setaria glauca could grow with higher biomass in all the amended soils. The treatment of apatite combined with plants was more effective than lime and charcoal treatments in removing Cu and Cd from the contaminated soils by taking biomass into account. Apatite had the best sustainable effect on alleviating soil acidification. The Cu and Cd concentrations of CaCl₂-extractable and exchangeable fractions decreased with the application of amendments. Moreover, apatite and lime could effectively maintain the bioavailability of Cu and Cd low.

Conclusions

Apatite had a better sustainable effect on the remediation of heavy metal-contaminated soils than lime and charcoal. Although all the amendment treated soils did not reduce soil total concentrations of Cu and Cd, they could effectively reduce the environmental risk of the contaminated soils. The findings could be effectively used for in situ remediation of heavy metal-contaminated soils.

Purpose

The Al forms on maize and soybean roots were investigated to determine the main factors affecting the distribution of Al forms and its relationship with Al plant toxicity.

Materials and methods

Solution culture experiments were conducted to obtain the fresh roots of maize and soybean. KNO₃, citric acid, and HCl were used to extract the exchangeable, complexed, and precipitated forms of Al on the roots.

Results and discussion

The complexed Al was higher than the exchangeable and precipitated Al. Root CECs of soybean and maize were 77 and 55 cmol kg^?1, and functional groups on the soybean roots (262.4 cmol kg^?1) were greater than on maize roots (210.8 cmol kg^?1), which resulted in more exchangeable and complexed Al on soybean roots than on maize roots, and was one of the reasons for the increased Al toxicity to soybean. The total and exchangeable Al were the highest on the plant root tips and decreased gradually with increasing distance from the tips. Ca²⁺, Mg²⁺, and NH₄ ⁺ cations reduced the exchangeable Al on the roots. Oxalate and malate also reduced the adsorption and absorption of Al by roots, and the effect of oxalate was greater than malate.

Conclusions

Higher exchangeable and complexed Al on plant roots led to increased Al plant toxicity. Ca²⁺, Mg²⁺, and NH₄ ⁺ and oxalate and malate can effectively alleviate Al plant toxicity.

Purpose

The nature of dissolved organic matter (DOM) strongly influences heavy metal sorption onto soil. However, the constituents and structures of DOM change continuously as DOM is subjected to microbial decomposition and photodegradation at natural field scales. Thus, this study was designed to explore the effects of chemical changes of DOM on heavy metal sorption onto farmland soil in natural degradation.

Materials and methods

Fresh DOM (FDOM) and degraded DOM (DDOM) both were extracted from the straw of maize which was extensively planted in Loess Plateau, China. The characteristics of DOM were determined by Fourier transform infrared spectroscopy (FTIR), elemental analysis, excitation-emission matrix (EEM) fluorescence spectra, UV-visible spectra (UV-vis), nuclear magnetic resonance (NMR), and molecular weight analysis. Farmland loess soil in Loess Plateau and heavy metal Cu(II) which can easily form a complex with DOM in soil were employed to investigate the effects of DOM dynamic changes on Cu(II) sorption onto loess through batch tests.

Results and discussion

Compared with FDOM, DDOM changed significantly in composition including oxygen content, functional group species, aromatic properties, and molecular weight distribution. Oxygen content, aromaticity, and low-molecular-weight fraction (<3 kDa) decreased while aromatic substitution and high-molecular-weight fraction (>10 kDa) increased for DDOM. For these changes, the effects of FDOM and DDOM on heavy metal Cu(II) sorption onto loess were significantly different due to DOM-Cu(II) binding ability varied with FDOM degradation. FDOM promoted Cu(II) sorption onto loess at Cu(II) concentration below 400 mg l^?1 while inhibited above 400 mg l^?1, but DDOM always showed inhibition effects on Cu(II) sorption onto loess. Moreover, both the promotion and inhibition effects depended mainly on the initial concentrations and pH values of FDOM and DDOM.

Conclusions

The results of the present study demonstrate that chemical characteristics of FDOM and DDOM are greatly diverse in components, functional group species, molecular weight distribution, etc. although they are from the same source. The apparent differences can explain their distinct effects on copper sorption onto loess soil. Hence, future researches are supposed to focus on the dynamic changes of DOMs when evaluating their influence on heavy metals environmental behaviors under actual conditions.

Purpose

This study aimed to evaluate the effect of combination of alkyl polyglucoside (APG) and nitrilotriacetic acid (NTA) on improving the efficiency of phytoremediation for pyrene and lead (Pb) co-contaminated soil by Scirpus triqueter.

Materials and methods

Seedlings of S. triqueter with a similar size and biomass (3 g/pot) were grown on 2-month aged soil contaminated with 184.5 mg kg^?1of pyrene and 454.3 mg kg^?1 of Pb at pH?=?8.3. After growth for 10 days, different doses of APG and NTA were added into the soil. After 60 days, the height of plants, Pb concentrations in plants, and pyrene amounts in soil were determined.

Results and discussion

Combined application of NTA and APG with lower dosage (1 + 1 g kg^?1 soil and 1 + 2 g kg^?1 soil) had no notable negative influence on the growth of S. triqueter. Moreover, significant synergy on Pb accumulation in S. triqueter was achieved with APG and NTA combined application. Besides, the dissipation of pyrene from soil after 60-day planting was increased in APG and NTA treatments when compared with the control treatments. Application of APG alone or combined with NTA had greater effect on enhancing dissipation of pyrene from soil than NTA alone.

Conclusions

This study demonstrated that the remediation of Pb and pyrene co-contaminated soil by S. triqueter can be enhanced by combined application of APG and NTA. Long-term evaluation of this strategy is needed in co-contaminated field sites.

Purpose

Particularly in organic viticulture, copper compounds are intentionally released into the environment as fungicide, whereas uranium originates from conventional phosphate fertilization. Both activities contribute to the metal contamination in wine-growing areas. This pilot study aimed to better understand how soil properties influence the presence and environmental fate of copper and uranium with respect to viticultural management.

Materials and methods

We characterized metal binding forms, i.e., their association with different soil constituents, in organically and conventionally cultivated vineyard soils and adjacent upstream and downstream sediments. The available metal fraction and the fractions associated with manganese oxides, organic matter, iron oxides, and total contents were extracted sequentially.

Results and discussion

Total soil copper ranged from 200 to 1600 mg kg^?1 with higher contents in topsoil than subsoil. The majority of copper (42–82%) was bound to soil organic matter. In all fractions, copper contents were up to 2-fold higher in organic than in conventional vineyards, whereas the sediment concentrations were independent of the adjacent viticultural management. A net increase of copper in downstream sediments was found only when water-extractable organic carbon (WEOC) in an adjacent vineyard was elevated. With 11 ± 1 mg kg^?1, total uranium was 25% higher in conventional than in organic vineyard soils. Its affinity to iron or WEOC potentially rendered uranium mobile leading to a substantial discharge to downstream sediments.

Conclusions

Translocation of copper and uranium from vineyards into adjacent stream sediments may rather be attributed to WEOC and iron contents than the viticultural management. Follow-up studies should scrutinize the processes driving metal availability and transport as well as their interaction at the aquatic–terrestrial interface.

Purpose

The study aimed at comparing the effects of different water managements on soil Cd immobilization using palygorskite, which was significant for the selection of reasonable water condition.

Materials and methods

Field experiment was taken to discuss the in situ remediation effects of palygorskite on Cd-polluted paddy soils, under different water managements, using a series of variables, including pH and extractable Cd in soils, plant Cd, enzyme activity, and microorganism number in soils.

Results and discussion

In control group, the pH in continuous flooding was the highest under three water conditions, and compared to conventional irrigation, continuous flooding reduced brown rice Cd by 37.9%, and brown rice Cd in wetting irrigation increased by 31.0%. In palygorskite treated soils, at concentrations of 5, 10, and 15 g kg^?1, brown rice Cd reduced by 16.7, 44.4, and 55.6%; 13.8, 34.5, and 44.8%; and 13.1, 36.8, and 47.3% under continuous flooding, conventional irrigation, and wetting irrigation (p < 0.05), respectively. The enzyme activity and microbial number increased after applying palygorskite to paddy soils.

Conclusions

Continuous flooding was a good candidate as water management for soil Cd stabilization using palygorskite. Rise in soil enzyme activity and microbial number proved that ecological function regained after palygorskite application.

Purpose

Crop growth on sandy soils can be increased by claying. In modified sandy soils, the added clay is in the form of peds ranging in size from millimetres to centimetres creating a highly non-uniform matrix where ped size could influence nutrient availability and organic C binding. The aim of the study was to determine the effect of clay addition rate and ped size in residue amended sandy soil on soil respiration, nutrient availability and organic C retention.

Materials and methods

In this study, clay peds of 1, 2 or 3 mm size derived from a clay-rich Vertosol (73 % clay) were added to a sandy soil (3 % clay) at clay addition rates of 10 and 20 % w/w. After the addition of ground faba bean residue (C/N 37) at 10 g kg^?1, the soils were incubated for 45 days at 80 % of water-holding capacity.

Results and discussion

Clay addition had no consistent effect on cumulative respiration, but reduced NH₄ ⁺ availability with a greater reduction at 20 % compared to 10 % clay and with 1 and 2 mm compared to 3 mm peds. Sandy soil with clay peds had a greater maximum NH₄ ⁺ and P sorption capacity than sandy soil alone, and sorption capacity was higher at 20 % compared to 10 % clay addition and greater with 1 mm compared to 3 mm peds. Retrieval of clay peds at the end of the experiment showed ped breakdown during the experiment but also the formation of larger peds. Compared to the <53 μm fraction added at the start of the experiment, the total organic carbon (TOC) content of the <53 μm fraction was increased up to nearly two fold, particularly in the smaller peds (1 and 2 mm).

Conclusions

When sandy soils are amended with clay, N availability and organic C binding depend on both clay addition rate and ped size.

Purpose

The phosphate adsorption on natural adsorbents is of particular importance in regulating the transport and bioavailability of phosphates in environmental system. In soils, oxides are often associated with organic matter and form mineral-organic complexes. The aim of the present paper was to investigate the mechanisms of phosphate adsorption on these complexes.

Materials and methods

Phosphate adsorption on uncoated and humic acid (HA)-coated iron oxide complexes was investigated at different ionic strengths and pH by isotherm experiments and attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy.

Results and discussion

Results showed that HA-coated iron oxide complexes caused a decrease in the specific surface area (SSA) and the isoelectric point (IEP) of oxides. Phosphate adsorption on iron oxides was insensitive to changes of ionic strength, while it increased on the complexes with increasing ionic strength. The presence of HA decreased the maximum adsorption and the affinity of phosphate on the complexes. The zeta potential of phosphate-bound iron oxides linearly reduced with the increment of phosphate surface coverage, while the zeta potential of complexes with adsorbed phosphate kept at the same level. ATR-FTIR analysis suggested the formation of phosphate-metal complexation. The presence of HA promotes the formation of the monodentate phosphate complexes at pH 4.5 and significantly influenced phosphate species at pH 8.5.

Conclusions

The amount of phosphate adsorbed was reduced, and the phosphate speciation was also influenced when phosphate was adsorbed on HA-coated iron oxide complexes compared with phosphate adsorption on pure goethite and hematite.

Purpose

The validity of soil erosion data is often questioned because of the variation between replicates. This paper aims to evaluate the relevance of interreplicate variability to soil and soil organic carbon (SOC) erosion over prolonged rainfall.

Materials and methods

Two silty loams were subjected to simulated rainfall of 30 mm h^?1 for 360 min. The entire rainfall event was repeated ten times to enable statistical analysis of the variability of the runoff and soil erosion rates.

Results and discussion

The results show that, as selective removal of depositional particles and crust formation progressively stabilized the soil surface, the interreplicate variability of runoff and soil erosion rates declined considerably over rainfall time. Yet, even after the maximum runoff and erosion rates were reached, the interreplicate variability still remained between 15 and 39 %, indicating the existence of significant inherent variability in soil erosion experiments.

Conclusions

Great caution must be paid when applying soil and SOC erosion data after averaging from a small number of replicates. While not readily applicable to other soil types or rainfall conditions, the great interreplicate variability observed in this study suggests that a large number of replicates is highly recommended to ensure the validity of average values, especially when extrapolating them to assess soil and SOC erosion risk in the field.

Purpose

At the global scale, gardening activities are often performed in urban areas with a historical background of pollution. In this study, a participatory program was developed with citizens concerned by gardening activities near a 50-year-old regulated lead recycling company, with the aim of co-constructing the tools for the assessment and management of potential sanitary risks induced by historic pollution with persistent (eco) toxic metals: lead and cadmium.

Materials and methods

Soils and vegetables (lettuce, leek, celery, carrot, chard, pumpkin, and celeriac) samples were collected from four kitchen gardens neighboring a 50-year-old secondary lead smelter. Both total and in vitro human bioaccessible metal concentrations in the cultivated plants were measured in relation to soil characteristics.

Results and discussion

The results showed that the soils of these gardens were slightly contaminated by metals (Pb, 77 to 236 mg kg^?1; and Cd, 0.5 to 1 mg kg^?1) in comparison with the natural geologic background. However, significant pollution of vegetables can occur especially with lead (Pb up to 9.8 mg kg^?1 in lettuce) and certainly as a result of direct foliar transfer. The washing of plants before consumption is therefore recommended in the context of atmospheric fallout of ultrafine particles enriched with metals.

Conclusions

Metal bioaccessibility measure integrates the influence of metal type, plant type, and soil physico-chemical properties. Based on the results, it is proposed that human bioaccessible fraction of metals may also be currently taken into account as well as total metal quantities and bioaccumulation factors in risk assessment studies performed in gardens. Overall, this study has led to reflections and functional recommendations aimed at reducing human exposure and to finally developing sustainable gardening practices.