The aim of this work was to study the level and degree of mobility of heavy metals in the soil–plant system and to perform bioindication observations in the Don River estuarine region and the Russian sector of the Taganrog Bay coast.
Materials and methodsThe objects of the study included samples of zonal soils (chernozem) and intrazonal soils (alluvial meadow and alluvial-stratified soils, Solonchak, sandy primitive soil) from monitoring stations of the Don river estuarine region and the Taganrog Bay coast, as well as their higher plants: Phragmites australis Cav., Typha angustifolia L., Carex riparia Curtis, Cichorium intybus L., Bolboschoenus maritimus L. Palla, and Rumex confertus Willd. The total concentrations of Mn, Ni, Cd, Cu, Zn, Pb, and Cr in the soils were determined by X-ray fluorescent scanning spectrometer. The concentration of heavy metal mobile forms exchangeable, complex compounds, and acid-soluble metal were extracted using the following reagents: 1 N NH4Ac, pH 4.8; 1 % EDTA in NH4Ac, pH 4.8; 1 N HCl, respectively. Heavy metals in plants were prepared for analysis by dry combustion at 450 °C. The heavy metal concentration in extracts from plants and soils was determined by AAS.
Results and discussionThe total contents of heavy metals in the soil may be described with a successively decreasing series: Mn?>?Cr?>?Zn?>?Ni?>?Cu?>?Pb?>?As?>?Cd. The total concentrations of As, Cd, and Zn in the soil exceed the maximum permissible concentrations levels. Contamination of alluvial soils in the estuarine zone with mobile Сu, Zn, Pb, and Cd has been revealed, which is confirmed by the high bioavailability of Cu and Zn and, to a lesser degree, Cd and Pb accumulating in the tissues of macrophytic plants. Data on the translocation of elements to plant organs have showed their predominant accumulation in the roots. Bioindication by the morphofunctional parameters of macrophytic plants (with a Typha L. species as an example) can be used for revealing the existence of impact zones with elevated contents of metals in aquatic ecosystems.
ConclusionsThe results revealed that increased content of Zn, Pb, Cu, Ni, and As in soil have anthropogenic sources. The high content of Cr in the soils is related to the lithogenic factor and, hence, has a natural source.
相似文献This study aimed to reveal spatial distribution of As, Cd, Cr, Cu, Mn, Ni, Pb, Sb, V, and Zn in paddy soils in the Zijiang River basin and to evaluate its pollution status and potential ecological risks, and thus to provide basic information for rational utilization of paddy soils in the study area.
Materials and methodsThe heavy metal(loid) concentrations in one hundred and thirty-five paddy soil samples (these samples were collected from the top 0–20 cm layer) were measured by inductively coupled plasma-optical emission spectrometry. The spatial distribution characteristics of the heavy metal(loid)s were depicted by the Ordinary Kriging interpolation analysis. The contamination degree and potential ecological risks of the heavy metal(loid)s in paddy soils were assessed by Nemerow’s comprehensive index, geoaccumulation index, potential ecological risk factor, and potential ecological risk index. The potential sources of the heavy metal(loid)s were deduced by Pearson’s correlation analysis, hierarchical cluster analysis, and principal component analysis.
Results and discussionThe mean concentrations of the heavy metal(loid)s decreased in the order of Mn?>?V?≈?Zn?>?Cr?>?Ni?≈?Pb?>?Cu?≈?Sb?>?As?>?Cd. Except for Cd and Sb, the mean concentrations of As, Cr, Cu, Mn, Ni, Pb, V, and Zn were close to the background reference values. The concentration of Cd in 94.8% of samples exceeded the soil quality standard value (grade II, 5.5?<?pH?<?6.5, GB 15618–1995). According to the assessments of pollution and potential ecological risks for the heavy metal(loid)s, 45.2% and 46.7% of samples were severely polluted and moderately polluted, respectively. The potential sources analysis indicated that Cd, Sb, and Zn mainly originated from agricultural, mining, and smelting activities; As, Cu, and Pb mainly originated from agricultural activities, while coal combustion by-products was another major source of these heavy metal(loid)s in paddy soils near the thermal power plant in the southwest corner of the study area; Cr, V, Mn, and Ni mainly originated from natural source.
ConclusionsCadmium and Sb are the main contaminants in paddy soils in the study area, and there are hot-spot pollution areas.
相似文献There is little knowledge on the organic matter fractions of salt-affected soil aggregates. This study aimed at investigating characteristics of salt-affected soil organic carbon components and the relationships between soil salt concentration and soil organic carbon component content.
Materials and methodsFive typical salt-affected soils in Hetao region China were collected and analyzed for light (LF) and heavy fraction (HF) in different water-stable aggregates. And the soil organic carbon components were measured by Fourier transform infrared (FTIR) and pyrolysis-gas chromatography/mass spectrometer (Py–GC/MS).
Results and discussionThe results showed that the salt-affected soils were dominant in 53–10-μm water-stable aggregates, 61–80% in the bulk soil, and very low in >?250-μm macro-aggregates, less than 7.06% in the bulk soil. The proportions of >?250-μm macro-aggregates and the mean weight diameter (MWD) were negatively correlated to Na+ concentration (p?<?0.05). Furthermore, the macro-aggregates were generally higher in total organic carbon (TOC) and accordingly higher C/N ratio than those in micro-aggregates. Heavy fractions (HF) from both >?53 μm and <?53-μm soil aggregates accounted for 99.30–99.83% of the bulk soil and contained 89.6–98.5% lower TOC and accordingly 49.2–84.8% lower C/N ratio than those in light fractions (LF). The LFs were high in lignin (7.27–34.02% in total pyrolysis products, 19.89% on average) and alkane/alkene-derived compounds (9.51–37.21%, 23.18% on average), but low in N-containing compounds (0–3.64%, 1.71% on average), while HFs were high in both alkane/alkene (4.38–27.46%, 15.06% on average) and N-containing compounds (7.45–26.45%, 13.98% on average), but low in lignin-derived compounds (1.13–8.75%, 3.86% on average).
ConclusionsThe tested salt-affected soils were predominant in 53–10-μm micro-aggregates, which was caused by the Na+ dispersion effect on soil aggregates. Most SOM was stored in HF that contained high N-containing compounds and low C/N ratios. Our results suggested that the components of SOM were mainly controlled by the soil Na+ concentration.
相似文献Several interactions between Al and the solid phase of soil influence Al buffering in soil solution. This work evaluated soils cultivated with Pinus taeda L. to determine Al forms in organic and mineral horizons using various extraction methods and to relate acidity with clay mineralogy.
Materials and methodsOrganic and mineral horizons of 10 soil profiles (up to 2.1 m deep) in southern Brazil were sampled. Organic horizons were separated into fresh, aged, and fermented/humified litter. The following Al extraction methods were utilized: 0.5 mol L?1 pH 2.8 CuCl2–Al complexed in organic matter; 1.0 mol L?1 KCl–exchangeable Al; water–Al soluble in soil solution; HF concentrated?+?HNO3 concentrated?+?H2O2 30% (v/v)–total Al. Six sequential extractions were carried out to isolate different forms of amorphous minerals that can buffer Al on soil solution: 0.05 and 0.1 mol L?1 sodium pyrophosphate; 0.1 and 0.2 mol L?1 ammonium oxalate; 0.25 and 0.5 mol L?1 NaOH. Samples of clay were also analyzed by XRD.
Results and discussionThere was a clear effect of litter age on increasing total Al concentration. In the aged litter and fermented and/or humified litter, levels of total Al were 1.4 to 3.8 and 1.5 to 7.8 times greater than in fresh litter, respectively. The CuCl2 method had higher Al extraction capacity than the KCl method for litter. The lowest Al–pyrophosphate values were observed in the Oxisol, which also had a predominance of gibbsite and the lowest levels of Al–KCl and Al–CuCl2. There was an inverse relationship between degree of soil weathering and soluble and exchangeable Al in soils. Available Al increased with higher Si proportion in minerals of the clay fraction (2:1?>?1:1?>?0:1).
ConclusionsThe worst scenario was soils with the combination of high soluble and exchangeable Al levels and high concentrations of amorphous forms of Al minerals. The best predictors of Al accumulation in the youngest litter horizon were extractions of amorphous minerals with pyrophosphate and NaOH. These extractors are normally used to predict the level of Al buffering in soils. Organic matter had less influence on Al dynamics in soils.
相似文献Soil consists of various sizes of aggregates, and different soil aggregates vary in their abilities to adsorb or transport metals. This study aimed to investigate the distribution behaviors of Cu from different fungicides in soil aggregates after a 15-month incubation.
Materials and methodsBordeaux mixture (CuSO4/Ca(OH)2?=?1/1 by weight, BR), copper nitrate (Cu(NO3)2·4H2O, CN), and copper oxychloride (3Cu(OH)2·CuCl2, CO) were applied to a representative Chinese Mollisol to reach the Cu content 200 mg kg?1. Five soil aggregate fractions, i.e., >?2000 μm, 2000–1000 μm, 1000–500 μm, 500–250 μm, and <?250 μm, were obtained by the wet sieving method. The modified Bureau Communautaire de Références (BCR) sequential extraction was applied to assess the Cu distribution among the main soil fractions.
Results and discussionThe highest Cu mass loading was found for the >?2000-μm soil aggregate. The input Cu was mainly in stable fractions, and the highest proportion was found for the residual fraction. The bioavailability and mobility of Cu from different fungicides in soils varied from each other, and they presented an order of CO > CN > BR. High bioavailability and transferring coefficients were found in the <?250-μm and >?2000-μm soil aggregates.
ConclusionsThis study indicated that the input Cu from fungicides mainly distributed in the >?2000-μm soil aggregates. Moreover, the CO-derived Cu presented a higher availability than the BR- and CN-derived Cu in the soil.
相似文献The purpose of this study is to study the major sources, concentrations, and distributions of polycyclic aromatic hydrocarbons (PAHs) in three different types of green space in Shanghai. In addition, we will quantitatively assess the burden of PAHs in the soil, as well as the potential carcinogenic risk of PAHs in humans. These results will provide valuable information for soil remediation and human health risk management.
Materials and methodsA total of 166 surface soil samples were collected in parks, greenbelts, and woodlands. Soils were extracted using accelerated solvent extraction (ASE). PAHs were analyzed by gas chromatography-mass spectrometry (GC-MS). The positive matrix factorization (PMF) model was used to identify major PAH emission sources and quantitatively assess their contributions to PAHs. The incremental lifetime cancer risk (ILCR) was used to quantify the potential health risk of PAHs.
Results and discussionThe average concentrations of ∑15 PAHs are 227?±?95 ng g?1, 1632?±?251 ng g?1, and 1888?±?552 ng g?1 in the woodland, park, and greenbelt soils, respectively. The PMF results show that biomass (33%), coal (21%), vehicles (17%), natural gas (14%), oil (9%), and coke (7%) are the dominant sources of PAHs in the park soils. Diesel (40%), tire debris (30%), biomass (15%), gasoline (9%), and oil (5%) are the main sources in the greenbelt soils. Biomass (48%), vehicles (37%), and coal (15%) are the main sources in the woodland soils. The ILCRs of adults and children who are exposed to PAHs in soils range from 9.53?×?10?8~1.42?×?10?5.
ConclusionIn three types of green space in Shanghai, the dominant PAHs are high–molecular weight (HMW) compounds (≥?4 rings). This may be due to the proximity of the sampling site to emission sources. In addition, low–molecular weight (LMW) PAHs (with 2–3 rings) are relatively unstable, and these compounds are prone to volatilization and degradation. Source identification indicates that biomass combustion is the most dominant PAH source in the park and woodland soils, while vehicles are the dominant PAH source in the greenbelt soils. The ILCRs of adults and children indicate potential health risks, and children have a greater health risk than adults.
相似文献Recent research suggests that Swedish organic arable soils have been under-recognized as a potential source of phosphorus (P) loading to water bodies. The aim of this study was to compare P losses through leaching from organic and high-fertility mineral soils. In addition, the effectiveness of a magnesium-salt-coated biochar applied below the topsoil as a mitigation strategy for reducing P losses was evaluated.
Materials and methodsPhosphorus leaching was measured from four medium- to high-P arable soils, two Typic Haplosaprists (organic 1 and 2), a Typic Hapludalf (sand), and an unclassified loam textured soil (loam), in a 17-month field study utilizing 90-cm-long lysimeters. A magnesium-salt-coated biochar was produced and characterized using X-ray powder diffraction (XPD), scanning electron microscopy with energy-dispersive spectroscopy (SEM-EDS), and X-ray adsorption (XANES) spectroscopy, and its phosphate adsorption capacity was determined at laboratory scale. It was also applied as a 3-cm layer, 27 cm below the soil surface of the same lysimeters and examined as a mitigation measure to reduce P leaching.
Results and discussionTotal-P loads from the 17-month, unamended lysimeters were in the order of organic 2 (1.2 kg ha?1)?>?organic 1 (1.0 kg ha?1)?>?sand (0.3 kg ha?1)?>?loam (0.2 kg ha?1). Macropore flow, humic matter competition for sorption sites, and fewer sorption sites likely caused higher P losses from the organic soils. Analysis by XRD and SEM revealed magnesium was primarily deposited as periclase (MgO) on the biochar surface but hydrated to brucite (Mg(OH)2) in water. The Langmuir maximum adsorption capacity (Qmax) of the coated biochar was 65.4 mg P g?1. Lysimeters produced mixed results, with a 74% (P?<?0.05), 51% (NS), and 30% (NS) reduction in phosphate-P from the organic 1, organic 2, and sand, respectively, while P leaching increased by 230% (NS) from the loam.
ConclusionsThe findings of this study indicate that P leached from organic arable soils can be greater than from mineral soils, and therefore, these organic soils require further investigation into reducing their P losses. Metal-enriched biochar, applied as an adsorptive layer below the topsoil, has the potential to reduce P losses from medium- to high-P organic soils but appear to be less useful in mineral soils.
相似文献This study compares the dynamic effects of straw and biochar on soil acidity and phosphorus (P) availability in the rice growth period to reveal how straw and biochar affect the availability of phosphorus in soil and utilization of P for rice crop.
Materials and methodsIn the pot experiment, rice straw, canola stalk, and corresponding biochars were mixed uniformly with the Ultisol. Soil samples were collected at four stages of rice growth to analyze the dynamic changes of soil acidity and P availability. The availability of phosphate in straw/biochar-amended soils were evaluated using a combination of chemical extraction and diffusive gradients in thin films (DGT) technique.
ResultsSoil pH, KCl-P, Olsen-P, DGT-P, and Al-P deceased with the rice growth, while Fe-P increased. Biochar increased soil pH and P availability more than straw returning, especially in the mature stage, while the DGT-P only increased in the tillering stage. The DGT-induced fluxes in sediments (DIFS) model revealed that all treatments increased the capacity of soil solid phase supplementing P to pore water in the filling and mature stages. The content of total P in different rice tissues followed the order of grain?>?straw?>?root, and RB350 treatment had the highest P content in rice tissues. In the mature stage, soil pH had positive correlations with KCl-P and Olsen-P, and soil Fe-P had positive correlations with total P of root and straw.
ConclusionsApplication of biochar made at 550 ℃ resulted in a larger increase in available P in soil, while biochar made at 350 ℃ had more effect on the chemical forms of P. The canola stalk biochar showed a larger influence on the P availability than rice straw biochar. Biochar treatments had a larger effect on inhibiting soil acidification and improving P availability than straw returning directly.
相似文献Climate warming and sea level rise have the potential to change the salt level of soil in tidal wetlands. And it is important to clarify the process and the mechanism of decomposition of soil organic carbon in a tidal wetland under varying salinities. The aim of this study was to evaluate the impacts of soil salinity on the decomposition rate of organic carbon (DROC) and dissolved organic carbon (DOC) in a tidal wetland.
Materials and methodsTwo types of soil (surface soil in Suaeda salsa and bare tidal flat) were collected, air-dried, and homogenized. After adding different content of salt (0 g/L, 3 g/L, 6 g/L, 9 g/L, and 12 g/L), the soils were incubated for 28 days at stable room temperature (25?±?2 °C) and added by deionized water to maintain the stability of soil moisture. The gases (CO2 and CH4) emission rates of each salt treatment were measured during 28-day incubation. DROC was determined by the sum of daily CO2-C emission rates and daily CH4-C emission rates in this study.
Results and discussionSalt addition inhibited the process of gas emissions and DROC. Gases emission rates and DROC of two types of soil showed similar temporal trends, with distinctive drop in the beginning of experiment and no significant decrease followed. Significant difference of DOC among salt treatments was found in the bare tidal flat soil. Variations of partial correlation between DROC and soil salinity and DOC showed similar trends (e.g., in days 9–18, the positive effect of DOC on DROC was greatly promoted (R2?=?0.80, p?<?0.001), and the negative effect of soil salinity was highly improved (R2?=?0.93, p?<?0.001)). Soil properties, in particular DOC, may be primary factors accounting for the discrepancy of gases emission rates and DROC of two types of soil.
ConclusionsIncreased soil salinity had a negative effect on DROC during 28-day incubation. The impact of soil salinity and DOC on DROC were varied in different phases of laboratory experiment (soil salinity generally had increasingly negative relationship with DROC, but DOC showed most significantly positive relationship in the middle stage of incubation). Both the formation and consumption of DOC may be valuable for more detail research regarding to decomposition of soil organic carbon.
相似文献The suppression effect of a sandy soil interlayer on topsoil enrichment of salt ions was investigated. However, whether this suppression effect was enhanced by surface mulching was little documented. The objectives of this study were to compare the suppression effects under different materials mulching, and to investigate an innovative method to suppress the soil salt ions down-to-top enrichment.
Materials and methodsIn this study, the sandy soil layer was pre-positioned at 60–100 cm depth in a salt-contaminated site in advance, achieving the suppression effect on surface enrichment of salt components as expected. Three treatments were herein designed as bare field (CK), plastic film mulching (PM), and maize straw mulching (SM) to examine the dynamics of water and salt movement across soil profiles during the summer with strong evaporation.
Results and discussionsResults showed that total salt content was increased by 21.3 and 8.0% in CK and SM respectively, while decreased by 24.9% in PM at the end of strong evaporation period, comparing with the beginning. Thus, surface mulching further strengthened this suppression effect, but PM displayed better performance than SM did. The data also demonstrated that vertical transport of soil water was much restrained in PM and SM, accordingly inhibiting upward transfer of salt ions. Particularly, sodium adsorption ratio (SAR) ranged from 14.3–265.7, 17.9–147.1, 38.4–147.2 mmol1/2 kg?1/2 at a shallow soil layer (0–60 cm) in CK, PM, and SM, respectively.
ConclusionsThe results suggested that sandy soil interlayer settings with plastic mulching are a critical technical strategy for salt-contaminated land reutilization and management.
相似文献Based on two consecutive years of field-scale trials, under different water managements, we illustrated the persistence of remediation effect of palygorskite on a Cd-polluted rice field.
Materials and methodsThe Cd uptake by a plant, pH and Cd chemical extractability, available P/K, and extractable Zn/Cu in paddy soils were used to evaluate the influence of palygorskite on Cd immobilization and soil fertility index.
Results and discussionIn contrast to the 1st year, at 0–1.5% palygorskite applied dose in soils, 0.025 M HCl–extractable Cd in continuous flooding reduced by 12.1–19.0%, and that in wetting irrigation increased by 10.9–18.9% in the 2nd year (p?<?0.05). The toxicity characteristic leaching procedure Cd reduction of 3.0–11.4% and increase of 8.9–12.0% were obtained under above-mentioned water managements (p?<?0.05). Compared with the 1st year, at different clay additional concentrations, grain Cd in continuous flooding reduced by 7.0–11.3%, and that in wetting irrigation increased by 6.5–10.8% in the 2nd year (p?<?0.05). Although trace elements in clay treated soils declined, they had no influence on the grain yield due to a minimum value higher than the critical value of 1.5 mg kg?1 for Zn and 2.0 mg kg?1 for Cu. The available P in continuous flooding took on a maximum increase of 8.2% in the 2nd year (p?<?0.05).
ConclusionsTwo consecutive years of field-scale in situ demonstration tests revealed that continuous flooding was a preferable water management regime for Cd immobilization using palygorskite in the rice field. There were no remarkable differences in extractable Zn/Cu between 2 years.
相似文献