The change of heavy metals fractions during hydrochar decomposition in soils amended with different municipal sewage sludge hydrochars

Purpose

This study was to investigate the changes of heavy metals in the soils amended with different municipal sewage sludge hydrochars.

Materials and methods

Sewage sludge hydrochars prepared at either 190 or 260 °C, for 1, 6, 12, 18, or 24 h, respectively, were added to soil samples and then incubated for 60 days. Water-extractable organic carbon (WEOC) and CO₂ evolution were determined during the incubation. The total quantities of heavy metals and their different fractions were analyzed by inductively coupled plasma spectrometry (ICP).

Results and discussion

Hydrochar-amended soils had much higher water-extractable carbon and more CO₂ evolution than control soil, indicating that the added hydrochars contained a significant amount of WEOC and could be decomposed during the incubation. Hydrochar addition immediately and significantly increased the total heavy metals of the soil. Moreover, both oxidizable and residual fractions of all heavy metals were significantly higher in all the hydrochar-added soils than those in control soil. Both oxidable and residual fractions of heavy metals decreased in the hydrochar-amended soils during 60-day incubation. In contrary, both acid soluble and reducible fractions of heavy metals increased in the hydrochar-amended soils during incubation. It is thus obvious that the heavy metals in both oxidable and residual fractions may be released during hydrochar decomposition and then be adsorbed by soil matrix such as carbonates, iron oxides, and clays.

Conclusions

Municipal sewage sludge can be readily carbonized into hydrochar. However, it is watchful of applying the hydrochar into soil since hydrochar addition increases in both total and bioavailable heavy metals in soil. More work is particularly required to investigate the long-term impacts on soil and environment.

     

Dry cultivation enhances cadmium solubility in contaminated soils but minimizes cadmium accumulation in a leafy vegetable

Purpose

Water management has a strong influence on Cd solubility in agricultural soils, affecting Cd uptake in crops. In the process, sulfur interaction with other metals such as zinc may play an important role. A pot experiment was carried out to investigate the effects of water management coupled with zinc and sulfate amendment on Cd uptake by the leafy vegetable amaranth with a strong Cd accumulation tendency in its edible parts.

Materials and methods

The soils were amended with Cd, Cd+SO₄ and Cd+SO₄+Zn with no amendment as control. Then, the soils were flooded for 1 month, after which amaranth was grown with soil kept saturated (wet cultivation). In the succeeding planting, soils were tilled to aeration condition under which amaranth was grown again (dry cultivation). Soil and crop samples were collected and analysed for various parameters.

Results and discussion

The readily exchangeable quantities of Cd and Zn in the soil decreased under wet cultivation, increasing again under dry cultivation but to levels lower than those in the initial soil. Wet cultivation enhanced plant Cd concentration but reduced Zn accumulation compared to dry cultivation. Zn bioavailability was strongly affected by soil water status but failed to reduce Cd uptake by amaranth. Irreversible or slowly reversible changes occurred in Cd and Zn solubility and phytoavailability as soil water-saturated status was altered by periodic flooding events.

Conclusions

Dry cultivation with lower soil water content ensured high production with low Cd in the edible part of this leaf vegetable and so remains the recommended irrigation regime.

     

Sustainability of in situ remediation of Cu- and Cd-contaminated soils with one-time application of amendments in Guixi,China

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.

     

Bioavailability of Cd and Zn in soils treated with biochars derived from tobacco stalk and dead pigs

Purpose

Previous studies show that application of biochar can reduce the bioavailability of heavy metals in soil. A plant growth experiment was carried out to evaluate the effect of tobacco stalk- and dead pig-derived biochars on the extractability and redistribution of cadmium (Cd) and zinc (Zn) in contaminated soil, and the impact on tobacco (Nicotiana tabacum L.) plant growth.

Materials and methods

The top 20 cm of a soil contaminated with Cd and Zn was used in this study. Biochars derived from tobacco stalk and dead pig were applied to the soil at four application rates (0, 1, 2.5, and 5 %), and tobacco plants were grown. After 80-days growth, the pH, electrical conductivity (EC), CaCl₂-extractable heavy metals and fractions of heavy metals in soil samples, as well as the plant biomass and the concentrations of heavy metals in the plant were determined.

Results and discussion

The plant growth experiment demonstrated that tobacco stalk biochar and dead pig biochar significantly (P?<?0.05) increased the pH, but had no significant effect on the electrical conductivity (EC) of the soil. The CaCl₂-extractable Cd and Zn content decreased as the application rates increased. The concentration of extractable Cd and Zn decreased by 64.2 and 94.9 %, respectively, for the tobacco stalk biochar treatment, and 45.8 and 61.8 %, respectively, for the dead pig biochar treatment at 5 % application rate. After biochar addition, the exchangeable Cd was mainly transformed to fractions bound to carbonates and Fe-Mn oxides, while the Zn was immobilized mainly in the fraction bound to Fe-Mn oxides. Tobacco stalk biochar increased the tobacco plant biomass by 30.3 and 36.2 % for shoot and root, respectively at the 5 % application rate. Dead pig biochar increased the tobacco plant biomass by 43.5 and 40.9 % for shoot and root, respectively, at the 2.5 % application rate. Both biochars significantly (P?<?0.05) decreased the Cd and Zn accumulation by tobacco plant.

Conclusions

As a soil amendment, tobacco stalk biochar was more effective at removing Cd, whereas dead pig biochar was more effective at removing Zn, and a higher application rate was more effective than a lower application rate. Overall, biochar derived from tobacco stalk was more effective, than dead pig biochar, at remediating soil contaminated with Cd and Zn, as well as promoting tobacco growth.

     

Contrast effect of long-term fertilization on SOC and SIC stocks and distribution in different soil particle-size fractions

Purpose

The objectives of the study were (1) to quantify the long-term effects of nitrogen-phosphorus fertilizer (NP) and a combination of nitrogen-phosphorus with organic manure (NPM) on total soil organic carbon (SOC) and total soil inorganic carbon (SIC), (2) to identify the changes of SOC and SIC in soil particle-size fractions, and (3) to investigate the relationship between SOC and SIC.

Materials and methods

Two long-term field experiments (sites A and B) were performed in 1984 (site A) and 1979 (site B) in the North China Plain. The soil samples were collected in 2006 and separated for clay, silt and sand size particle fractions and then determined for SOC and SIC.

Results and discussion

The long-term fertilization significantly increased SOC in 0–20 cm soil layer by 9–68% but significantly decreased or had no effect on SIC. In total, soil carbon storage was little affected by NP, but significantly increased by NPM application (p < 0.05). Fertilization affected both SOC and SIC in sand- and silt-sized particles but not in clay-size fraction. Both NP and NPM increased SOC in sand- and silt-sized particles by 8.7–123.9% in the 0–20 cm layer but decreased SIC up to 80.4% in the 40–60 cm layer. The SOC concentration in the particle-size fractions was negatively correlated with SIC concentration, which may imply an antagonistic interaction between organic and inorganic carbon levels.

Conclusions

These results illustrate the importance of soil inorganic carbon pool in evaluating soil total carbon pool in semi-arid farmlands. Previous assessments of the effects of fertilizers on the soil carbon pool, using only SOC determinations, require re-evaluation with the inclusion of SIC determinations.

     

Heavy metal distribution in different soil aggregate size classes from restored brackish marsh,oil exploitation zone,and tidal mud flat of the Yellow River Delta

Purpose

Heavy metal distribution in soils is affected by soil aggregate fractionation. This study aimed to demons trate the aggregate-associated heavy metal concentrations and fractionations in “sandy,” “normal,” and “mud” soils from the restored brackish tidal marsh, oil exploitation zone, and tidal mudflat of the Yellow River Delta (YRD), China.

Materials and methods

Soil samples were sieved into the aggregates of >2, 0.25–2, 0.053–0.25, and <0.053 mm to determine the concentrations of exchangeable (F1), carbonate-bound (F2), reducible (F3), organic-bound (F4), and residual fraction (F5) of Cd, Cr, Cu, Ni, Pb, and Zn.

Results and discussion

The 0.25–2 mm aggregates presented the highest concentrations but the lowest mass loadings (4.23–12.18 %) for most metal fractions due to low percentages of 0.25–2 mm aggregates (1.85–3.12 %) in soils. Aggregates <0.053 mm took majority mass loadings of metals in sandy and normal soils (62.04–86.95 %). Most soil aggregates had residual Cr, Cu, Ni, Zn, and reducible Cd, Pb dominated in the total Cd, Cr, Cu, Ni, Pb, and Zn concentrations. Sandy soil contained relatively high F4, especially of Cu (F4) in 0.25–2 mm aggregates (10.22 mg kg^?1), which may relate to significantly high organic carbon contents (23.92 g kg^?1, P?<?0.05). Normal soil had the highest total concentrations of metals, especially of Cu, Ni, and Pb, which was attributed to the high F3 and F5 in the <0.053 mm aggregates. Although mud soil showed low total concentrations of heavy metals, the relatively high concentrations of bioavailable Cd and Cu resulted from the relatively high Cd (F2) and Cu (F2) in the >2 mm aggregates indicated contribution of carbonates to soil aggregation and metal adsorption in tidal mud flat.

Conclusions

Soil type and aggregate distribution were important factors controlling heavy metal concentration and fractionation in YRD wetland soil. Compared with mud soil, normal soil contained increased concentrations of F5 and F3 of metals in the 0.053–0.25 mm aggregate, and sandy soil contained increased concentrations of bioavailable and total Cr, Ni, and Zn with great contribution of mass loadings in the <0.053 mm aggregate. The results of this study suggested that oil exploitation and wetland restoration activities may influence the retention characteristics of heavy metals in tidal soils through variation of soil type and aggregate fractions.

     

Changes of soil particle size fraction along a chronosequence in sandy desertified land: a fundamental process for ecosystem succession and ecological restoration

Purpose

Soil is composed of particles of different sizes. A fraction of soil particles with different sizes has many vital effects on soil properties such as soil texture, soil porosity, and soil nutrient content. We intended to explore what change took place in soil particle distribution along the chronosequence of restoration and to address what implication this change has for ecosystem restoration.

Materials and methods

Six restoration ecosystem sites were selected to form a chronosequence in a sandy desertified region, northern China. We examined the relative content of soil particles with different sizes and established an index of enrichment ratio to reflect the change trend of soil particle size fraction.

Results and discussion

It was showed that soil substrate in this region is mainly composed of coarse sand (>0.25 mm) and fine sand (0.25–0.10 mm), the fraction of which are averagely 23.62 and 57.07 %, respectively. These characteristics make soil coarse, loose and erodible, and to be one of the reasons why sandy desertification was quickly developed in this region. In sandy desertification process, the grades of soil particles were air-classified. Fine sand was strongly enriched 1.36 times than average level, while very fine sand (0.10–0.05 mm) and silt and clay (<0.05 mm) were strongly diluted 0.14 and 0.22 times than average level, respectively. Along with the chronosequence of restoration, very fine sand and silt and clay were deposited and markedly enriched. This change in soil particle size fraction along the chronosequence has many fundamental roles for the subsequent restoration succession of sandy land ecosystem, such as promoting plant growth, strengthening soil anti-erodibility, leading to species replacement and community succession.

Conclusions

From this research, it could be concluded that the response of soil particle size fraction to ecological restoration in sandy desertified lands is ecologically valuable, demonstrating that a positive cycle between plant and soil was formed to strengthen the stability of soil-plant system, and the ecosystem has the ability of self-recovering or self-organizing.

     

Rhizosphere effects of <Emphasis Type="Italic">Populus euramericana</Emphasis> Dorskamp on the mobility of Zn,Pb and Cd in contaminated technosols

Purpose

This study aimed at investigating the rhizosphere effects of Populus euramericana Dorskamp on the mobility of Zn, Pb and Cd in contaminated technosols from a former smelting site.

Materials and methods

A rhizobox experiment was conducted with poplars, where the plant stem cuttings were grown in contaminated technosols for 2 months under glasshouse conditions. After plant growth, rhizosphere and bulk soil pore water (SPW) were sampled together. SPW properties such as pH, dissolved organic carbon (DOC) and total dissolved concentrations of Zn, Pb and Cd were determined. The concentrations of Zn, Pb and Cd in plant organs were also determined.

Results and discussion

Rhizosphere SPW pH increased for all studied soils by 0.3 to 0.6 units compared to bulk soils. A significant increase was also observed for DOC concentrations regardless of the soil type or total metal concentrations, which might be attributed to the plant root activity. For all studied soils, the rhizosphere SPW metal concentrations decreased significantly after plant growth compared to bulk soils which might be attributed to the increase in pH and effects of root exudates. Zn, Pb and Cd accumulated in plant organs and the higher metal concentrations were found in plant roots compared to plant shoots.

Conclusions

The restricted transfer of the studied metals to the plant shoots confirms the potential role of this species in the immobilization of these metals. Thus, P. euramericana Dorskamp can be used for phytostabilization of technosols.

     

Simultaneous immobilization of lead,cadmium, and arsenic in combined contaminated soil with iron hydroxyl phosphate

Purpose

Combined contamination of lead (Pb), cadmium (Cd), and arsenic (As) in soils especially wastewater-irrigated soil causes environmental concern. The aim of this study is to develop a soil amendment for simultaneous immobilization of Pb, Cd, and As in combinative contaminated soil.

Materials and methods

A soil amendment of iron hydroxyl phosphate (FeHP) was prepared and characterized, and its potential application in simultaneous immobilization of Pb, Cd, and As in combined contaminated soil from wastewater-irrigated area was evaluated. The effects of FeHP dosage, reaction time, and soil moisture on Pb, Cd, and As immobilization in the soil were examined.

Results and discussion

The immobilization efficiencies of Pb, Cd, and As generally increased with the increasing of FeHP dosage. With FeHP dosage of 10 %, the immobilization percentages of NaHCO₃-extractable As and DTPA-extractable Pb and Cd reached 69, 59, and 44 %, respectively. The equilibrium time required for immobilization of these contaminants was in the following order: NaHCO₃-extractable As (0.25 days) < DTPA-extractable Cd(3 days) < DTPA-extractable Pb (7 days). However, the immobilization efficiencies of Pb, Cd, and As have not changed much under soil moisture varied from 20 to 100 %. According to the results of the sequential extraction, the percentages of Pb, Cd, and As in residual fractions increased after the application of FeHP amendment, while their percentages in exchangeable fractions decreased, illustrating that FeHP can effectively decrease the mobilities and bioavailabilities of Pb, Cd, and As in the soil. Moreover, the application of FeHP will not have soil acidification and soil structure problem based on the soil pH measurements and soil morphology.

Conclusions

FeHP can immobilize Pb, Cd, and As in the combinative contaminated soil from wastewater irrigation area simultaneously and effectively. Thus, it can be used as a potential soil amendment for the remediation of Pb, Cd, and As-combined contaminated soil.

     

Evaluation of palygorskite for remediation of Cd-polluted soil with different water conditions

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.

     

Mixed chelators of EDTA,GLDA, and citric acid as washing agent effectively remove Cd,Zn, Pb,and Cu from soils

Purpose

Soil washing with chelators is a viable treatment alternative for remediating multi-contaminated soils. The aim of this study was to investigate the removal efficiencies of Cd, Zn, Pb, and Cu in alkaline and acid multi-metal-contaminated soils by washing with the mixed chelators (MC).

Materials and methods

The batch experiments were carried out to evaluate the removal efficiencies of heavy metals in contaminated soils by the MC with different molar ratios of EDTA, GLDA, and citric acid, and evaluated the washing factors, including contact time, pH, MC concentration, and single and multiple washings at the same MC dose, on the removal efficiencies.

Results and discussion

Results showed that the removal efficiencies for Cd, Zn, Pb, and Cu by the MC (the molar ratio of EDTA, GLDA, and citric acid was 1:1:3) were as much as those of the only EDTA washing from both soil at the same application dose of total chelators; moreover, the application dose of EDTA decreased by 80%. For the alkaline-contaminated soil, the removal efficiencies of Cd, Zn, Pb, and Cu decreased with the increasing of the solution pH, which was opposite to acid-contaminated soil. This was attributed to that the metal-ligand complex could be obviously re-adsorbed on the soil surface sites, particularly in low pH values. The removal efficiencies of Cd, Zn, Pb, and Cu depended on MC concentration. A higher MC concentration led to a more effective removal of Cd, Zn, Pb, and Cu in alkaline-contaminated soil; however, their changes were slightly increased in acid-contaminated soil. At the same dose of MC, single washing with higher MC concentration might be favorable to remove heavy metals, moreover, with much less wastewater generation.

Conclusions

The MC (the molar ratio of EDTA, GLDA, and citric acid was 1:1:3) may be a useful, environmentally friendly, and cost-effective chelators to remediate heavily multi-metal-contaminated soil.

     

Influence of organic and inorganic passivators on Cd and Pb stabilization and microbial biomass in a contaminated paddy soil

Purpose

Soil contamination with heavy metals, such as Cd and Pb, has caused severe health and environmental risks all over the world. Possible eco-friendly solutions for Cd and Pb immobilization were required to reduce its mobility through various cost-effective amendments.

Materials and methods

A laboratory incubation study was conducted to assess the efficiency of biochar (BC), zeolite (ZE), and rock phosphate (RP) as passivators for the stabilization of Cd and Pb in paddy soil as well as soil microbial biomass. Various extraction techniques were carried out: a sequential extraction procedure, the European Community Bureau of Reference (BCR), toxicity characteristic leaching procedure (TCLP) test, and single extraction with CaCl₂. The impact of passivators on soil pH, dissolved organic carbon (DOC), and microbial biomass (carbon, nitrogen, and phosphorus) was examined in the metal contaminated soil.

Results and discussion

The results showed that the exchangeable portion of Cd in soil was significantly reduced by 34.8, 21.6, and 18.8% with ZE, RP, and BC at a 3% application rate, respectively. A similar tendency of reduction in Pb soluble portion was observed by ZE (9.6%), RP (20%), and BC (21.4%) at a 3% application rate. Moreover, the TCLP leachate of Cd and Pb was apparently reduced by 17 and 30.3% with BC at a 3% application dose, respectively, when compared to the control. Soil pH, nutrients, and microbial biomass C, N, and P were significantly increased with the addition of BC, RP, and ZE passivators.

Conclusions

The results showed that the incorporation of BC, ZE, and RP significantly reduced the Cd and Pb mobility in paddy soil as well as enhanced soil nutrients and microbial biomass. Overall, among all the amendments, rice straw derived-BC performed better for Cd and Pb immobilization in paddy soil.

     

Effect of tea plantation age on the distribution of fluoride and its fractions within soil aggregates in the hilly region of Western Sichuan,China

Purpose

Long-term tea plantation (Camellia sinensis L.) could markedly change the pools of total fluoride (T-F) in soil extractable fractions. However, the effects of different chronosequence phases on the changes of fluoride fractions in these plantations are poorly understood.

Materials and methods

In this study, we have investigated the distribution of extractable fluoride fractions in four differently aged tea plantations (16, 23, 31, and 53 years old, respectively), in Zhongfeng Township of Ming-shan County, Sichuan, Southwest China. This study aimed to determine the effects of the age of various tea plantations with respect the contents of T-F, also considering the water-soluble fluoride (Ws-F), the exchangeable fluoride (Ex-F), the Fe/Mn oxide-bound fluoride (Fe/Mn-F), the organic matter-bound fluoride (Or-F), and the residual fluoride (Res-F) within soil aggregates.

Results and discussion

The T-F, Ws-F, Ex-F, and Res-F contents increased with the decreasing of particle size except for Fe/Mn-F and Or-F. Along with the increase of tea plant life, the contents of Ws-F and Ex-F within soil aggregates gradually increased. In addition, the trends of extractable Fe/Mn-F and Or-F were opposite to that of highly available fluoride after 23 years.

Conclusions

The results of this study show that fluoride is easily transformed into highly available phases in long-term tea plantations, improving the absorption of fluoride for tea plants.

     

Evaluating the fraction of electrically associated cations on surfaces of soil particles by extrapolation of strong-field Wien effect measurements in dilute suspensions

Purpose

For agricultural production and environment protection, it is cations loosely bound to the soil particles that have a great significance in short-term processes of adsorption–desorption, exchange, and transport. It is beneficial to be able to evaluate the fractions of these cations in order to correctly predict potential pollution of soils by heavy metals and availability of plant nutrients.

Materials and methods

The homionic suspensions of yellow-brown soil (YB) and black soil I (BI) saturated with Na⁺ and Ca²⁺ and three subsamples of black soil II (BII) saturated with Ca²⁺ and Cd²⁺ were prepared to determine the electrical conductivity (EC) of the suspensions. On the basis of electrical conductivity vs. field strength (EC-E) curve, the fraction of electrically associated cations on surfaces of soil particles was evaluated by extrapolation of strong-field Wien effect measurements in dilute suspensions.

Results and discussion

The maximum dissociation degree (α _max) of Na⁺ adsorbed on surfaces of yellow-brown soil and black soil I was about 0.21, which is approximately twice as much as those of Ca²⁺ (0.07–0.10) adsorbed on surfaces of two soils. The soil type was not the main factor in evaluating α _max, and the valence of the cations was. For divalent cations, α _max of Ca²⁺ and Cd²⁺ adsorbed on soil particles with different contents of organic matter descended in the order: top black soil II?>?bottom black soil II?>?OM-free bottom black soil II.

Conclusions

The relatively small fractions of electrically adsorbed cations—about 0.2 for Na⁺ and 0.1 for Ca²⁺ on yellow-brown and black soils particles indicated that even for the more loosely adsorbed Na⁺ ions, most of the cations in the double layers of soil particles were adsorbed strongly by other, more specific mechanisms and cannot be stripped off into the solution, which would increase its electrical conductivity in a strong applied field.

     

Remediation of heavy metal(loid)s contaminated sediments—in situ iron treatment and subsequent magnetic extraction

Purpose

Surface sediments contaminated with high levels of multiple heavy metal(loid) species are very common environmental problems. Especially, the labile and bioaccessible fractions of heavy metal(loid)s in the sediments are posing serious risks to the biota and the overlaying water quality. This study aimed at developing a potential method to manage the activity of the labile fractions of heavy metal(loid)s in surface sediments.

Materials and methods

This study assessed the feasibility of adding iron powder, a low-cost industrial by-product, to sediments containing high levels of Pb, As, and Cd to adsorb labile fractions of heavy metal(loid)s onto the sorbent surfaces and to retrieve the heavy metal(loid) laden powders by applying external magnetic field. In addition, the redistribution of Pb, Cd, and As in different sediment fractions, the dissolved fraction and the sorbent-adsorbed fraction, was also investigated and characterized.

Results and discussion

The results indicate that the bioactive labile fractions (exchangeable and carbonate-bound fractions) of heavy metal(loid)s are prone to concentrating onto iron powders and can be selectively removed from the sediments by magnetic retrieval. In addition, iron addition induces conversion of labile fractions of heavy metal(loid)s into more stabilized fractions.

Conclusions

Overall, the process can effectively minimize the activity of labile fractions of heavy metal(loid)s in surface sediments.

     

Source identification and apportionment of soil cadmium in cropland of Eastern China: a combined approach of models and geographic information system

Purpose

Cadmium (Cd) is regarded as one of the most toxic heavy metals in the environment and can undermine the ecosystem function and human health at trace level due to its high toxicity. In order to reduce the anthropogenic Cd input into agricultural soil, it is of utmost importance to pinpoint the sources of Cd in soils and apportion their respective contributions.

Materials and methods

One hundred twenty-seven topsoil samples and 21 subsoil samples were collected from croplands of Meishan Basin, Changxing County, Zhejiang Province, Eastern China, and analyzed for concentrations of Cd and other heavy metals. Finite mixture distribution model (FMDM) was employed to fit the data to obtain the local soil Cd threshold value, a critical indicator to assess soil heavy metal contamination. Then, principal component analysis (PCA) and geographic information system (GIS) were used to identify the potential sources of Cd. Finally, positive matrix factorization (PMF) was applied to apportion the source contributions.

Results and discussion

Among the 127 topsoil samples, 71 were subject to Cd contamination with a mean concentration of 0.66 mg kg^?1 while the others were considered as background with a lower mean concentration of 0.145 mg kg^?1, close to the local background concentration of 0.142 mg kg^?1. Further, three components were extracted by PCA and interpreted as natural background, lead-acid battery manufacturing plants, and construction material associated activities, respectively. Additionally, most of the topsoil samples around the lead-acid battery manufacturing plants, construction material plants, and limestone/marble quarries were classified as Cd contaminated. However, PMF failed to get a successful portioning.

Conclusions

Lead-acid battery manufacturing plants and construction material associated activities were the main anthropogenic sources of soil Cd contamination. With the help of FMDM, it is possible to distinguish the contaminated soil and estimate the contribution of anthropogenic sources to soil Cd. The apportionment by PMF was not successful in this paper due to the high skewness or outliers of Cd concentration in sampling sites and violation of the assumption that all samples have the same sources.

     

Organic carbon and nitrogen dynamics in different soil fractions between broad-leaved Korean pine forests and aspen–birch forests in northeastern China

Purpose

Both overharvesting and climate changes have greatly altered forest composition in northeastern China; however, forest-specific effects on soil organic carbon (SOC), N, and compositional features in different soil fractions have not yet been defined.

Materials and methods

By sampling from broad-leaved Korean pine forest (the climax vegetation) and aspen–birch forest (the secondary forest), five soil fractions were separated by a physicochemical soil fractionation method, and Fourier transform infrared spectroscopy, X-ray diffraction analysis, and X-ray photoelectron spectrometry were used for functional groups, mineral diffraction, and elemental composition determination together with SOC and N measurements.

Results and discussion

Aspen–birch forests tended to sequestrate more SOC in the slow fractions (sand and aggregate [SA] and easily oxidized fractions) and more N in the sensitive fractions (particulate and soluble fractions), indicating that in aspen–birch forests, high SOC sequestration (1.26-fold) coincided with the active and rapid N supply. Much higher percentages (13.1–40.5 %) of O–H and N–H stretching, O–H bending, and C=O, COO–, and C–H stretching, and also the much lower quartz grain size and mineral diffraction peaks in SA and acid-insoluble fraction (over 85 % of total soil mass), in aspen–birch forests were possibly associated with the 1.17- to 1.53-fold higher SOC compared to broad-leaved Korean pine forest. However, elemental composition on soil particles might marginally contribute to the SOC and N forest-dependent differences.

Conclusions

Considering the increase of aspen–birch forests and the decrease of broad-leaved Korean pine forests in historical and future scenarios in northeastern China, more SOC has been and also will sequestrate in intact soils and stable soil fractions, with more N in sensitive fractions, and these should be highlighted in evaluating forest C and N dynamics during forest successions in this region.

     

Binding,fractionation, and distribution of Cs,Co, and Sr in a US coastal soil under saturated and field capacity moisture regimes

Purpose

The concerns of the public on safe handling of nuclear energy power facilities have increased due to the recent nuclear plant accidents in Japan and others. Cesium, cobalt, and strontium are a few of the major radionuclides released from nuclear power plant accidents. The objectives of this study are to investigate binding, distribution, fractionation, and transformation of cesium (Cs), cobalt (Co), and strontium (Sr) in a US coastal soil under saturated paste (SP) and field capacity (FC) moisture regimes.

Materials and methods

There are four major nuclear power plants in the coast region around the northern Gulf of Mexico where coastal soil often undergoes soil moisture change. A coastal soil was taken from the middle region of these major nuclear power plants and spiked with different concentrations of cesium, cobalt, and strontium salts. The sequential selective dissolution technique was used to investigate the transformation and fractionations of these metals in the coastal soils affected by moisture regime, a key factor in the coastal environment.

Results and discussion

The adsorption kinetics showed that both Co and Sr reached the adsorption plateau even after 5 h of adsorption, indicating a fast initial adsorption process in the coastal soil. Cesium, cobalt, and strontium were dominantly presented in the soluble and exchangeable form (EXC) (Cs?>?Co and Sr), which linearly increased with the addition levels, possessing the high bioavailability, mobility, and ecotoxicity. Saturated regime significantly reduced the soluble and exchangeable form compared to field capacity moisture regime.

Conclusions

The current study provides the fundamental understanding for designing the cost-effective remediation technology to remediate these metals in coastal soil by targeting on the soluble and exchangeable forms and better prepare the USA for future potentially nuclear power plant accidents.

     

Magnetic signature and source identification of heavy metal contamination in urban soils of steel industrial city,Northeast China

Purpose

Identifying the spatial distribution and degree of heavy metal contamination in the soils is required for urban environmental management. Magnetic measurement provides a rapid means of determining spatial distribution and degree of soil pollution and identifying various anthropogenic sources of heavy metals. The purpose of this study was to characterize the magnetic signature of heavy metal contamination and identify the sources of heavy metals in urban soils from steel industrial city.

Materials and methods

A total of 115 urban topsoils from Anshan city, Northeast China, were collected and determined for magnetic properties and heavy metal concentration. Magnetic susceptibility (χlf) and saturation isothermal remanent magnetization (SIRM) were determined as proxy for ferrimagnetic mineral concentration. Magnetic minerals were identified by using Curie temperature, X-ray diffraction (XRD), and scanning electron microscope (SEM) equipped with an energy-dispersive X-ray spectrometer (EDS). The Pearson’ correlation and matrix cluster analyses were used to establish the relationship between magnetic parameters and heavy metal concentrations.

Results and discussion

Urban topsoils exhibit characteristic magnetic enhancement. The magnetic measurement in particle size fractions indicates that 50–2 μm fraction has the highest low-field magnetic susceptibility (χlf), while <2 μm has the highest frequency-dependent magnetic susceptibility (χfd) value. The soil χlf and SIRM values are significantly correlated with the contents of metals (Fe, Pb, Zn, Cu, and Cr) and Tomlinson pollution load index (PLI), which indicates that χlf and SIRM could be served as better indicators for the pollution of heavy metals in the urban topsoil. Spatial distribution maps of χlf, SIRM, and PLI indicate that the pollution hotspots tend to associate with the regions within and close to steel industrial zones. XRD and Curie temperature analyses indicate that the main magnetic minerals of urban topsoils are magnetite (Fe₃O₄), hematite (α-Fe₂O₃), and metallic iron. Magnetic minerals mostly occur in the pseudo-single-domain/multidomain (PSD/MD) grain size range, which is the dominant contributor to the magnetic enhancement of topsoils. SEM observation reveals that magnetic particles in soils exist in irregular-shaped particles and spherule. Results reveal that heavy metals from industrially derived and traffic emissions coexist with coarse-grained magnetic phases.

Conclusions

It is concluded that the magnetic measurement could be regarded as a proxy tool to detect the level of heavy metal pollution and identify the source of heavy metals in urban soils. Magnetic properties provide a fast and inexpensive method to map the spatial distribution of long-term pollution from steel industrial origin on region scale.

     

Effect of aggregation on the adsorption of phosphorus onto air-dried sediment in contrasting shear flow conditions

Purpose

Fine sediments are usually collected in situ and air-dried for adsorption experiments, which may lead to particle aggregation and thus have a significant effect on phosphorus (P) adsorption under dynamic conditions. The main purpose of this study was to investigate the changes of aggregates due to drying with shear stress and the effects on the adsorption of P onto air-dried sediments under different shear rates after re-wetting.

Materials and methods

Sediment samples were collected from an alluvial river. Fine wet sediments (<31 μm) were wet-sieved and air-dried, and some air-dried sediments were further sonicated and served as the control. The grain size distribution of the three sediment samples (wet, dried, and sonicated) was measured to evaluate the particle aggregation level. The P sorption capacity of wet and dried sediments was determined by batch equilibrium experiments. The change of aggregate size with shear stress was investigated for dried and sonicated sediments. Sorption equilibrium experiments were performed to investigate the effect of shear stress on the P sorption with and without change of particle aggregation level, respectively.

Results and discussion

Fine particles agglomerated into larger aggregates during the drying process, resulting in a significant increase in the aggregate size. The sorption capacity was lower in aggregated sediment than in original wet sediment. Aggregate size in dried sediment decreased with the increase of shear rate, leading to an increase in the surface area and available adsorption sites, whereas the particle size of sonicated sediment was hardly affected. Accordingly, the P sorption amount of dried sediment increased with increasing shear rate, whereas that of sonicated sediment showed no significant change with shear rate after all sediments were suspended. There was a significant curvilinear correlation between aggregate size and P sorption amount for dried sediments, thus indicating that the P sorption amount increased significantly with decreasing aggregate size.

Conclusions

Sediment aggregation is an important factor affecting P adsorption besides the amount of suspended sediments and the exchange between suspended and bed sediments under dynamic conditions. The P equilibrium adsorption amount increases with shear stress for air-dried sediment. The effect of particle aggregation on the amount of P sorbed onto sediments should not be ignored, and thus, more attention should be paid to the pretreatment of sediment samples in the sorption experiments under dynamic conditions.