Crops grow poorly in saline-sodic soils, and the productivity of these soils can be dramatically improved with proper amendments. Current research mainly focuses on either organic or inorganic soil amendments, whereas few studies address options of combining organic and inorganic amendments. The objective of this study was to develop new organic and inorganic soil amendments which can lower the soil pH, replace sodium, and improve soil structure.
Materials and methodsPolyhalite (PL), microporous potassium-silicon-calcium mineral fertilizer (MF), furfural residue (FR), and fulvic acid (FA) were mixed with four different ratios to produce organic and inorganic soil amendments: PLFR, PLFA, MFFR, and MFFA. And their optimum mixing ratios were determined by comparing the potassium, calcium concentrations, and pH of filtrate after dissolution. Then, a leaching experiment was conducted by packing mixtures (mass ratio of soil to amendment = 219:1, equivalent to 13 t/hm2) of the saline-sodic soil with each one of these amendments plus two contrasts, gypsum (GP), and no amendment (CK). And the remediation effect was compared by pH, EC, ESP, texture, organic recombination degree of clay, saturated hydraulic conductivity, water-stable aggregates fraction, and enzyme (urease, alkaline phosphatase, and catalase) activities of soil.
Results and discussionAfter four times leaching experiment, soil treated with PLFR had lower pH and 25.86% lower exchangeable sodium than untreated soils. The water-stable small macroaggregate fractions and saturated hydraulic conductivity of the MFFR-treated soils were significantly increased by 133% and 31%, respectively. Also, the total soil and heavy fraction organic carbons of the soils treated with MFFR in addition to its alkaline phosphatase activity were all significantly higher than the other treatments.
ConclusionsThe results revealed that MFFR has more potential as a soil amendment to improve soil structure and quality and thus help in the development and use of saline-sodic lands for agriculture.
相似文献This study focused on the effects and mechanisms of biochar amendment to Cd-contaminated soil on the uptake and translocation of Cd by rice under flooding conditions.
Materials and methodsPot and batch experiments were conducted using Cd-contaminated soil collected from a field near an ore mining area and a cultivar of Oryza sativa ssp. indica. Biochar derived from rice straw under anaerobic conditions at 500 °C for 2 h was mixed with the soil at the rate of 0, 2.5, and 5%.
Results and discussionThe application of 5% biochar reduced CaCl2-extractable soil Cd by 34% but increased Cd concentration in brown rice by 451%. Biochar amendment decreased water-soluble Fe2+ in soils and formation of Fe plaques on roots and weakened the Fe2+-Cd2+ competition at adsorption sites on the root surface. Biochar increased water-soluble Cd in the soil and consequently Cd uptake by rice roots by releasing water-soluble Cl?. Biochar application also reduced the proportion of cell wall-bound Cd in the root, which caused easier Cd translocation from the cortex to the stele in the root and up to the shoot.
ConclusionsRice straw biochar (with high concentration of water-soluble Cl?) reduced CaCl2-extractable soil Cd but increased Cd concentration in rice under flooding condition.
相似文献Polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs) in Havana were quantified and analyzed in relation to possible emission sources to assess metropolitan soil contaminations in a highly dynamic, urban environment. The results of this study will serve Cuban legislators as a basis to develop environmental quality standards for organic pollutants in soils.
Materials and methodsPossible emission sources as, e.g., the vicinity to roads or industrial plants and the influence of the land use were related to the organic contaminants concentrations. Therefore, 28 topsoils in the Havana urban and semi-urban area were sampled at agricultural (n?=?12), organoponic (urban gardens in the capital, n?=?8), public park (n?=?7), and remediation (on-site bioremediation of an oil refinery, n?=?1) sites. Their PAH and PCB concentrations were measured with gas chromatography mass spectroscopy and the total organic carbon (TOC) and black carbon (BC) concentrations with the chemo-thermal oxidation.
Results and discussionThe sum of the 16 PAH concentrations ranged from 0.04 mg/kg in agricultural and organoponic soils to up to 72 mg/kg in a public park at about 1.5 km distance from an oil refinery. The lowest sum of the seven PCB congener concentrations was also measured in organoponic soils (0.002 mg/kg) and the highest in an arable patch of land between the rail roads and a main road (0.1 mg/kg). Both, PAH as well as PCB soil concentrations in Havana were almost up to two orders of magnitudes higher compared to a soil monitoring in the neighboring province of Mayabeque, but overall in the typical range of urban soils reported by other studies. The pollutants showed no relationship between TOC and BC except for PAHs with BC. For PAHs, combustion was the main source.
ConclusionsA comparison of the pollutant concentrations with regulatory guidance values (RGV) of other countries revealed PCB concentrations in Havana soils far below these RGV. In contrast, some concentrations of benzo[a]pyrene, the most carcinogenic PAH, in agricultural and park soils in Havana exceeded some RGV. Thus, some public parks pose a risk according to the Canadian quality guidelines when people have direct contact with these soils but not if they were consuming products thereof.
相似文献Phosphorus influence on arsenic bioavailability in soils and its toxicity to plants is widely recognized. This work compares competitive influence of P on As bioavailability in dry and flooded soils.
Materials and methodsPot experiments were carried out in dry and flooded soils, respectively. Bioavailable As in soils was measured using diffusive gradients in thin films (DGT), soil solution concentration, and three single chemical extraction methods.
Results and discussionP concentration at 50 mg/kg promoted wheat growth in dry soil. At concentrations above 50 mg/kg, P competition inhibited wheat growth and enhanced As toxicity. In flooded soil, the rice height and biomass decreased with the increase of P addition. P concentrations above 800 mg/kg were lethal to the rice. The content of As absorbed by wheat and rice roots as well as shoots increased with the increase of P concentration. The bioavailability of As in wheat- and rice-grown soils, determined by all methods, also increased with the increase of P concentration. The correlation analysis between the bioavailable As measured by the all three methods and the content of As in plants showed a significant positive correlation. The Pearson correlation coefficient for the DGT method was higher comparing to all other methods. DGT-induced fluxes in soils (DIFS) modeling further showed sharp decreases of Tc (the characteristic time to reach equilibrium between available solid As pool and soil solution As from DGT perturbation) and increases of desorption and adsorption rate constants (k1 and k?1) of As in P-amended soils, reflecting that the kinetic release of As from available solid As pools became much easy from P competition.
ConclusionsP competition in both dry and flooded soils could significantly increase bioavailability of As and further increase its toxicity. Competition effect was more pronounced in flooded soil. DGT is a more accurate method for As bioavailability evaluation in both dry and flooded soils.
相似文献The aim of this study was to investigate the remediation efficiency of actual arsenic-contaminated soils by electrokinetic (EK)-enhanced remediation with approaching cathode and Fe0 permeable reactive barrier (PRB).
Materials and methodsExperiments were conducted in a lab-made apparatus consisting of the anode reservoir, the soil specimen chamber, and the cathode reservoir.
Results and discussionIn this study, the enhanced combination methods (approaching cathode and Fe0-PRB) were assisted for EK remediation of actual arsenic-contaminated soils under a voltage gradient of 1 V/cm and a treatment period of 96 h. Experimental results showed that arsenic accumulated in the anode sections (I, II) of the soil by employing EK alone with an arsenic removal rate of less than 5%. In contrast, EK-enhanced remediation with either approaching cathode (EK/AC) or Fe0-PRB (EK/PRB) reduced the arsenic concentrations in both central and anode sections of the soil and afforded the removal rates of 20% in both cases. However, EK-enhanced remediation with the combination of approaching cathode and Fe0-PRB (EK/PRB/AC) reached the removal efficiency of 45% without arsenic accumulation in any soil sections. This phenomenon is mainly caused by the approaching cathode that creates an alkaline environment to promote the migration of arsenic, as well as PRB filled with Fe0 that achieves the adsorption and immobilization of arsenic.
ConclusionsThe highest remediation efficiency was achieved in the EK/PRB/AC test, which was attributed to the fact that the combination of this two methods solved the problem of arsenic accumulation in treated soil and ensured a more thorough arsenic removal. Furthermore, enhanced remediation efficiency does not elevate the costs.
相似文献Phosphorus (P) losses from agricultural fields through leaching are the main contributors to eutrophication of lakes and rivers in North America. Adoption of P-retaining strategies is essential to improve the environmental quality of water bodies. The main objective of this study is to evaluate lime as a soil amendment in reducing phosphorus concentration in the leachate from three common soil textures with neutral to alkaline pH.
Materials and methodsPhosphorus leaching from undisturbed soil columns (10 cm in diameter and 20 cm deep) as well as small repacked columns was investigated and compared in this study. Lime (high calcium hydrated lime) at the rate of 1% by air-dried soil mass was applied to the topsoil of the columns. Both sets of experiments followed a full factorial design with two factors of soil texture at three levels (sandy loam, loam, and clay loam) and treatment at two levels (control and limed) with three replicates. Scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy was performed on the control and limed soil samples to confirm the formation of calcium phosphate compounds.
Results and discussionsFor both intact and repacked columns, dissolved reactive phosphorus (DRP) concentrations in the leachates from limed sandy loam and limed loam soil columns was significantly reduced, while DRP in the limed clay loam column leachates was not changed. Elemental mapping demonstrated that in limed sandy loam and loam soils, the calcium loadings on the soil surface were always linked with phosphorus. The formation of calcium phosphate compounds and the increased phosphate adsorption on the soil surface through Ca bridging could be the two main phosphorus-lime retention mechanisms. Total dissolved phosphorus (TDP) in the leachates of limed loam and limed clay loam indoor intact and repacked columns was reduced, while there was no change in that of the sandy loam soil. In finer textured soils, lime can increase TDP retention through the immobilization of organic phosphates.
ConclusionsThe impact of lime application on DRP and TDP varied with the soil texture. The lime-induced reduction in the DRP and TDP was variable between the intact and repacked columns demonstrating the importance of soil structure on phosphorus and lime interactions in the soil. Overall, lime application at the studied rate can be considered a promising soil amendment in mitigating phosphorus loss from non-calcareous neutral to alkaline soils.
相似文献To compare Cd removal from different soils with three washing agents recovered from sewage sludge (dissolved organic matter (DOM), soluble humic-like substances (HLS), soluble humic substances (SHS)). Also, to investigate how washing with these agents changes soil organic-matter composition (OM).
Materials and methodsSandy clay loam (S1) and clay (S2) highly contaminated with Cd (300 mg kg?1) were washed with DOM, HLS, or SHS solutions at various pHs, and with various washing times and washing modes (single or double). Cd distribution and OM composition were determined (including content of humic substances (HS), fulvic fraction (FF), labile humic acids (L-HA), and stable humic acids (S-HA)).
Results and discussionCd removal proceeded with pseudo-second-order kinetics. Equilibrium was reached in 30 min (S1) and 60 min (S2). DOM, HLS, and SHS removed 75–82% of Cd from S1, and 80–87% from S2. The most mobile fraction of Cd was removed after one wash. S2 retained more OM, including HS, than S1. Although washing did not change the HA/FF ratio in most variants, washing with DOM and HLS increased the percentage of L-HA in both soils. Washing with SHS increased S-HA content in both soils, but the percent content of S-HA was similar to that in the unwashed soil.
ConclusionsDOM, HLS, and SHS derived from sewage sludge can effectively remediate clay and sandy clay soils highly contaminated with Cd. Washing with an SHS solution can increase the content of the most stable carbon forms (HA), which is beneficial for carbon sequestration in remediated soils.
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While organic waste amendments can initially improve soil physicochemical properties, including nutritional benefits to plants and increased microorganism activity, long-term application of excessive amounts of organic wastes can cause accumulation of heavy metals (HMs). Thus, the current study examined the accumulation of HMs in agricultural soil profiles following organic waste application.
Materials and methodsThree common organic sludge, including municipal sewage sludge (MSS), industrial sewage sludge (ISS), and leather sludge (LS), were applied annually to an agricultural soil under field conditions over 7 years (1994–2000) at a rate of 25 and 50 t ha?1 year?1. Subsequently, when organic sludge amendments were ceased, the experimental plots were cultivated without any treatments for another 12 years (2001–2012) and the changes in HM concentrations along the soil depth profile were monitored together with soil pH, dissolved organic carbon (DOC), and dehydrogenase activity (DHA).
Results and discussionSignificant increases in Cu, Pb, and Zn concentrations were observed down to a depth of 80 cm in soils treated with ISS and LS, where sludge application also increased the levels of Cd, Cr, Pb, and Zn and their movement down the soil profile. However, with the exception of Cu, no significant changes in HM concentrations were observed following treatment with MSS. At a depth of 80 cm, soils which had received 25 and 50 t ha?1 LS showed, respectively, 4 and 14 times higher Cr levels than the control soil.
ConclusionsOrganic sludge induced changes in soil pH and soil DOC concentration which were the key factors influencing HM movement and accumulation following organic sludge treatment.
相似文献Heavy metal pollution in soils has become a global environmental concern. The combination of biochar and compost has already been proved to be an attractive method in contaminated soil. The objective was to study the sorption-desorption characteristics of Cd, Cu, and Zn onto soil amended with combined biochar-compost.
Materials and methodsIn this study, the soil was amended with combinations of biochar and compost with different ratios at 10% (w/w). To determine the sorption-desorption behaviors of heavy metals by biochar-compost amendment with different ratios, we determine the effects of different ratios on soil properties and use batch experiments to investigate sorption-desorption behaviors of Cd, Cu, and Zn.
Results and discussionThe results show that the Langmuir and Freundlich model can well describe the adsorption isotherm of Cd, Cu, and Zn in the soils with or without biochar-compost combinations. The incorporation of amendment combinations into soil significantly promotes the sorption affinity of soil on metals. The sorption capacity of Cd and Zn was improved as the compost percentage rose in biochar-compost more likely due to the increase of organic matter and available phosphorus, while that of Cu was stronger with 10 and 20% biochar addition in biochar-compost combinations likely as the result of the formation of new specific adsorption sites and the mobile Cu adsorption in compost after adding a certain amount of biochar in amendment mixtures. Additionally, a certain proportion of biochar applied into amendment mixtures could suppress desorption of Cd and Cu by pH change, and the Zn desorption rate gradually decreased as the compost ratio increased in amendment mixtures.
ConclusionsThe results indicated that the various ratios between biochar and compost have a significant effect on sorption-desorption of metals in soil, which helps us consider the effective combination of biochar and compost in soil.
相似文献The concentrations and distribution of arsenic (As) in two different soil types (Vertisols and Entisols) of Central Mexico impacted by mine activities and irrigation with As-rich groundwater are analyzed in order to determine their impact on the soil quality, and to contribute reliable data that may help to assess the environmental risk that represents the progressive accumulation of As in the arable soils of Guanajuato.
Materials and methodsTwo Entisol and two Vertisol profiles located in the Guanajuato state (Mexico) were described and sampled from ~?1.20-m-deep pits. Soils are irrigated with As-rich deep and shallow groundwaters that were sampled from irrigation boreholes. Additionally, a Vertisol profile located in a parcel not impacted by irrigation was sampled and used as a control soil. Minerals were identified by X-ray diffraction (XRD) and scanning electron microscopy (SEM) coupled with dispersive X-ray spectrometry (EDS). Geoaccumulation indexes (Igeo) were calculated to evaluate As enrichment with respect to a control soil and the Upper Continental Crust (UCC). Anions and cations of groundwater were analyzed by high-performance liquid chromatography (HPLC) and by inductively coupled plasma atomic emission spectroscopy (ICP-AES), respectively. As in soils was determined by ICP-AES.
Results and discussionNear total As concentrations are higher in Entisols (mean As value?=?7.20 mg/kg) than in Vertisols (mean As?=?1.02 mg/kg). As concentrations in the control soil are lower (0.34 to 0.70 mg/kg). The in-depth distribution of As in Vertisol profiles reveals that the higher As concentrations are found in the uppermost horizons (10 cm) and they tend to decrease with depth. In Entisols, As concentrations do not follow a vertical trend. Igeo values of As indicate moderate to heavy As contamination in Vertisols and moderate contamination in Entisols. SEM-EDS analyses revealed the presence of some potential As-bearing minerals such as magnetite and abundant Fe oxides and Ti-Fe coatings precipitated onto feldspar grains, particularly in Entisols.
ConclusionsIrrigation of Vertisols with As-rich groundwater determines As concentrations in the uppermost horizons that exceed the natural background of the region (0.4 mg/kg). In depth, clay grain-sized particles inhibit the downward migration of As, while Fe oxides and organic matter scavenge As by adsorption. As concentrations in Entisols are higher, and the in-depth distribution of this element is controlled by periodic contributions of As-bearing minerals delivered from mine prospects located at the river’s catchments.
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Soil chromium (Cr) pollution has received substantial attention owing to related food chain health risks and possible promotion of greenhouse gas (GHG) emissions. The aim of the present study was to develop a promising remediation technology to alleviate Cr bioavailability and decrease GHG emissions in Cr-polluted paddy soil.
Materials and methodsWe investigated the potential role of biochar amendment in decreasing soil CO2, CH4, and N2O emissions, as well in reducing Cr uptake by rice grains at application rates of 0 t ha?1 (CK), 20 t ha?1 (BC20), and 40 t ha?1 (BC40) in Cr-polluted paddy soil in southeastern China. In addition, the soil aggregate size distribution, soil organic carbon (SOC) concentration of soil aggregates, soil available Cr concentration, and rice yield were analyzed after harvesting.
Results and discussionBiochar amendment significantly reduced CO2, CH4, and N2O emission fluxes. Compared to CK, total C emissions in the BC20 and BC40 treatments decreased by 9.94% and 17.13% for CO2-C, by 30.46% and 37.10% for CH4-C, and by 34.24% and 37.49% for N2O-N, respectively. Biochar amendment increased the proportion of both the 2000–200 μm and 200–20 μm size fractions in the soil aggregate distribution. Accordingly, the organic carbon concentration of these fractions increased, which increased the total SOC. Moreover, biochar amendment significantly decreased soil available Cr concentration and total Cr content of the rice grains by 33.6% and 14.81% in BC20 and 48.1% and 33.33% in BC40, respectively. Rice yield did not differ significantly between biochar amendment treatment and that of CK.
ConclusionsBiochar application reduced GHG emissions in paddy soil, which was attributed to its comprehensive effect on the soil properties, soil microbial community, and soil aggregates, as well as on the mobility of Cr. Overall, the present study demonstrates that biochar has a great potential to enhance soil carbon sequestration while reducing Cr accumulation in rice grains from Cr-polluted rice paddies.
相似文献Natural sepiolite (SP) has proven effective on the in-situ immobilization remediation of Cd-contaminated soils. But the practical remediation effect may largely influenced by water management and the application of organic manure. The effects of chicken manure (CM) on SP-amended soils were investigated under normal and saturated water conditions using a pot experiment with Brassica campestris L.
Materials and methodsCd-contaminated paddy soils were amended with CM, SP, and CM?+?SP with no amendment as control. The amount of sepiolite was 0.5% (w/w, the same below) either in SP or CM?+?SP amended soils, while the amount of CM was 0.5, 1.0, and 2.0% in CM and CM?+?SP-amended soils. The plant metal contents, fresh weight, and soluble sugar content of plant edible parts were measured on harvest. Soil Cd was extracted by diethylenetriaminepentaacetic acid (DTPA) and HCl to estimate the mobility of heavy metal. Soil pH and dissolved organic matter (DOM) of rhizosphere soil were determined. The electronegative charges of soils were also measured using the zeta potential.
Results and discussionThe application of CM and increasing soil moisture on SP-amended soil increased plant growth to a greater extent than the application of SP alone. The application of CM along with the increase of soil moisture decreased Cd uptake and translocation in plants grown on SP-amended soil compared to the application of SP alone. Cd content of edible plant parts reached a minimum of 0.24 mg kg?1 with the application of 2.0% CM on SP-amended soils under water-saturated conditions, which was approximately 50% lower than the Cd concentration found when applying SP alone.
ConclusionsThe results of this study suggest that the application of sepiolite on Cd contaminated soil can effectively reduce Cd uptake by B. campestris L., and the addition of CM combined with effective water management also appears to further reduce Cd absorption and accumulation.
相似文献Understanding the soil nitrogen (N) mineralization potential (N0) and crop N availability during the growing season is essential for improving nitrogen use efficiency (NUE) and preventing over-fertilization, which lead to negative environmental impacts.
MethodsFive black soils with different levels of fertility were selected in Northeast China. The N0 and kinetics of these soils were estimated through laboratory experiments at different incubation temperatures (15, 25, and 35 °C). N mineralization dynamics were simulated using field soil temperature according to the incubation results. Moreover, the N uptake dynamics of maize were simulated according to the literature.
ResultsCompared with the very low-fertility soils, the cumulative mineralized nitrogen increased under all incubation temperatures (15, 25, and 35 °C), by 48–136%, 8–61%, and 24–59%, respectively, in the medium- and high-fertility soils. The highest N0 values (96.90, 115.31, and 121.33 mg/kg at the three different temperatures) were recorded in the very high-fertility soils. The soil N mineralization dynamics and N uptake of maize in the growing season were highly consistent over time, although the soil N supply could not meet the maize growth requirements. The higher the soil fertility, the lower the N fertilizer requirement.
ConclusionsDifferent fertilizer strategies were developed based on the cumulative mineralized N, N uptake by maize, and NUE in soils with different fertility levels. We suggested a reduction of 50–65 kg N/ha in N fertilizer in the two highest fertility soils. This study provided basic data to reduce chemical N fertilizer to improve NUE and reduce negative environmental impacts.
相似文献Biochar has shown to be a great product to control the bioavailability of potentially hazardous elements (PHE) in contaminated soils. Despite the advantages associated with the application of biochar in agricultural soils, relatively few studies have focused on the effects of biochar amendments on soil chemical properties, accumulation of arsenic, cadmium, zinc, and lead in rice tissues, and their availability in soil systems.
Materials and methodsThe field experiment was conducted at the paddy soils in Hunan Province, China. The soil texture was sandy clay loam. Wheat-derived biochar was applied once to the experimental plots at the rates of 0, 10, 20, 30 and 40 t ha?1, and referenced as A0, A10, A20, A30, and A40, respectively. For PHE determination, soil samples and plant samples were digested with a mixed solution of HCl:HNO3 (4:1, V:V) and HCl:HClO4 (4:1, V:V), respectively, and the arsenic, cadmium, zinc, and lead in the digest solution were measured by ICP-MS (Thermo Fisher Scientific, USA). The soil available fraction of PHE (arsenic, cadmium, zinc, and lead) was extracted by diethylenetriamine pentaacetic acid (DTPA) and measured by inductively ICP-MS.
Results and discussionBiochar amendment increased chemical properties of soil organic matter, pH, electrical conductivity, cation exchange capacity, nitrate nitrogen, and available phosphorus. Soil DTPA extractable arsenic, cadmium, zinc, and lead concentrations were significantly reduced. Arsenic, cadmium, zinc, and lead in rice shoots, and arsenic, cadmium, and zinc in roots significantly decreased after amendment. Concentrations in rice tissues positively and negatively correlated with the soil available fraction of PHE and soil chemical properties, respectively. Soil electrical conductivity negatively correlated with the soil available fraction of PHE. Concentrations of arsenic, zinc, cadmium, and lead in rice roots declined relative to increases of cation exchange capacity (arsenic, zinc), available phosphorus (cadmium), and nitric nitrogen (lead) content. Similar relationships were observed between cation exchange capacity and PHE in shoots.
ConclusionsBiochar creates avoidance of PHE through regulating chemical properties through biochar sorption capacity. Cation exchange capacity, available phosphorus, and nitric nitrogen were the principle factors affecting roots uptake of arsenic, zinc, cadmium, and lead. Biochar soluble salts could decline availability of metals/metalloids in soils through precipitation. Wheat-derived biochar application is an alternative safe product to immobilize PHE in rice paddy soils by restricting the risk of PHE.
相似文献Copper (Cu) is the earliest anthropogenic metal pollutant, but knowledge of Cu soil concentrations at ancient metalworking sites is limited. The objective of this work was to examine the ability of portable X-ray fluorescence to quantify Cu in soils at such sites.
Materials and methodsUsing a Bruker Tracer III-SD pXRF, we examine factory “scan” settings versus simple instrument parameter changes (a reduction in energy settings from 40 to 12 kV) to target analysis for Cu. We apply these to a set of uncontaminated samples (n?=?18, <?92 mg Cu kg?1) from Central Thailand and compare results to standard wet chemistry analysis (aqua regia digestion and ICP-OES analysis). We then apply the optimized method to a set of highly contaminated samples (n?=?86, <?14,200 mg Cu kg?1) from a known ancient smelting site.
Results and discussionWe demonstrate that simple changes to factory recommended “scan” settings can double the sensitivity of Cu determination via pXRF (“optimized limit of determination” of 19.3 mg kg?1 versus an initial value of 39.4 mg kg?1) and dramatically improve the accuracy of analysis. Changes to other results for other elements are variable and depend on concentration ranges, soil matrix effects, and pXRF response for the individual element. We demonstrate that pXRF can accurately determine Cu across a wide concentration range and identify grossly contaminated soil samples.
ConclusionsWe conclude that pXRF is a useful tool to rapidly screen and analyse samples at remote sites and can be applied to ancient metalworking sites. Simple optimization of the pXRF settings greatly improves accuracy and is essential in determining comparative background concentrations and “unaffected” areas. Application to other elements requires further element and matrix specific optimization.
相似文献